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1.

rs1490880683 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    Y:13479646 (GRCh38)
    Y:15591526 (GRCh37)
    Canonical SPDI:
    NC_000024.10:13479645:G:A
    Gene:
    UTY (Varview), MIR12120 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,500B_downstream_variant,non_coding_transcript_variant,downstream_transcript_variant
    Validated:
    by frequency
    MAF:
    A=0.00002/1 (GnomAD_exomes)
    HGVS:
    NC_000024.10:g.13479646G>A, NC_000024.9:g.15591526G>A, XM_011531455.4:c.20C>T, XM_011531455.3:c.20C>T, XM_011531455.2:c.20C>T, XM_011531455.1:c.20C>T, XM_011531453.4:c.20C>T, XM_011531453.3:c.20C>T, XM_011531453.2:c.20C>T, XM_011531453.1:c.20C>T, XM_011531454.4:c.20C>T, XM_011531454.3:c.20C>T, XM_011531454.2:c.20C>T, XM_011531454.1:c.20C>T, NM_007125.4:c.20C>T, XM_011531441.4:c.20C>T, XM_011531441.3:c.20C>T, XM_011531441.2:c.20C>T, XM_011531441.1:c.20C>T, XM_011531442.4:c.20C>T, XM_011531442.3:c.20C>T, XM_011531442.2:c.20C>T, XM_011531442.1:c.20C>T, XM_011531443.4:c.20C>T, XM_011531443.3:c.20C>T, XM_011531443.2:c.20C>T, XM_011531443.1:c.20C>T, XM_011531445.4:c.20C>T, XM_011531445.3:c.20C>T, XM_011531445.2:c.20C>T, XM_011531445.1:c.20C>T, XM_011531446.4:c.20C>T, XM_011531446.3:c.20C>T, XM_011531446.2:c.20C>T, XM_011531446.1:c.20C>T, XM_011531447.4:c.20C>T, XM_011531447.3:c.20C>T, XM_011531447.2:c.20C>T, XM_011531447.1:c.20C>T, XM_011531448.4:c.20C>T, XM_011531448.3:c.20C>T, XM_011531448.2:c.20C>T, XM_011531448.1:c.20C>T, XM_011531451.4:c.20C>T, XM_011531451.3:c.20C>T, XM_011531451.2:c.20C>T, XM_011531451.1:c.20C>T, XM_011531459.4:c.20C>T, XM_011531459.3:c.20C>T, XM_011531459.2:c.20C>T, XM_011531459.1:c.20C>T, XM_011531460.4:c.20C>T, XM_011531460.3:c.20C>T, XM_011531460.2:c.20C>T, XM_011531460.1:c.20C>T, XM_017030070.3:c.20C>T, XM_017030070.2:c.20C>T, XM_017030070.1:c.20C>T, XM_017030071.3:c.20C>T, XM_017030071.2:c.20C>T, XM_017030071.1:c.20C>T, XM_017030073.3:c.20C>T, XM_017030073.2:c.20C>T, XM_017030073.1:c.20C>T, NM_001258249.2:c.20C>T, NM_001258249.1:c.20C>T, XM_047442748.1:c.20C>T, XM_047442749.1:c.20C>T, XM_047442751.1:c.20C>T, XM_047442752.1:c.20C>T, XM_047442754.1:c.20C>T, NR_047607.1:n.1025C>T, NR_047598.1:n.1025C>T, NR_047624.1:n.1025C>T, XM_047442747.1:c.20C>T, NR_047645.1:n.1025C>T, XM_047442750.1:c.20C>T, NR_047644.1:n.1025C>T, NM_001258258.1:c.20C>T, NR_047599.1:n.1025C>T, NM_001258252.1:c.20C>T, NM_001258261.1:c.20C>T, NR_047603.1:n.1025C>T, NR_047597.1:n.1025C>T, NR_047642.1:n.1025C>T, NR_047618.1:n.1025C>T, NM_001258260.1:c.20C>T, NM_001258264.1:c.20C>T, NR_047637.1:n.1025C>T, NR_047641.1:n.1025C>T, NM_001258266.1:c.20C>T, XM_047442753.1:c.20C>T, NM_001258251.1:c.20C>T, NM_001258267.1:c.20C>T, NR_047602.1:n.1025C>T, NM_001258256.1:c.20C>T, NR_047647.1:n.1025C>T, NM_001258259.1:c.20C>T, NR_047600.1:n.1025C>T, NM_001258262.1:c.20C>T, NR_047638.1:n.1025C>T, NM_001258253.1:c.20C>T, NR_047646.1:n.1025C>T, NM_001258269.1:c.20C>T, NM_001258263.1:c.20C>T, NR_047635.1:n.1025C>T, NM_001258268.1:c.20C>T, NR_047632.1:n.1025C>T, NM_001258255.1:c.20C>T, NR_047609.1:n.1025C>T, NM_001258265.1:c.20C>T, XM_047442746.1:c.20C>T, NM_001258270.1:c.20C>T, NM_001258257.1:c.20C>T, NR_047643.1:n.1025C>T, NM_001258254.1:c.20C>T, NM_001400177.1:c.20C>T, NM_001258250.1:c.20C>T, NR_047612.1:n.1025C>T, NM_001400175.1:c.20C>T, NM_001400178.1:c.20C>T, NR_047614.1:n.1025C>T, NR_047629.1:n.1025C>T, NR_047621.1:n.1025C>T, NR_047623.1:n.1025C>T, NR_047601.1:n.1025C>T, NR_047622.1:n.1025C>T, NR_047617.1:n.1025C>T, NR_047608.1:n.1025C>T, NR_047615.1:n.1025C>T, NR_047636.1:n.1025C>T, NR_047606.1:n.1025C>T, NR_047611.1:n.1025C>T, NR_047631.1:n.1025C>T, NR_047610.1:n.1025C>T, NR_047628.1:n.1025C>T, NM_001400181.1:c.20C>T, NR_047605.1:n.1025C>T, NR_047613.1:n.1025C>T, NR_047616.1:n.1025C>T, NR_047633.1:n.1025C>T, NR_047627.1:n.1025C>T, NR_047626.1:n.1025C>T, NR_047596.1:n.1025C>T, NR_047634.1:n.1025C>T, NR_047640.1:n.1025C>T, NR_047620.1:n.1025C>T, NR_047630.1:n.1025C>T, NR_047639.1:n.1025C>T, NR_047625.1:n.1025C>T, NR_047619.1:n.1025C>T, NR_047604.1:n.1025C>T, NM_001400170.1:c.20C>T, NM_001400171.1:c.20C>T, NM_001400173.1:c.20C>T, XM_047442755.1:c.20C>T, NM_182659.1:c.20C>T, XR_007068451.1:n.1025C>T, XM_047442756.1:c.20C>T, XR_007068452.1:n.1025C>T, NR_174404.1:n.388C>T, XM_047442757.1:c.20C>T, NR_174405.1:n.388C>T, NM_182660.1:c.20C>T, NM_001400183.1:c.20C>T, NM_001400185.1:c.20C>T, NM_001400187.1:c.20C>T, NM_001400189.1:c.20C>T, NM_001400192.1:c.20C>T, NM_001400195.1:c.20C>T, NM_001400199.1:c.20C>T, XP_011529757.1:p.Ser7Leu, XP_011529755.1:p.Ser7Leu, XP_011529756.1:p.Ser7Leu, NP_009056.3:p.Ser7Leu, XP_011529743.1:p.Ser7Leu, XP_011529744.1:p.Ser7Leu, XP_011529745.1:p.Ser7Leu, XP_011529747.1:p.Ser7Leu, XP_011529748.1:p.Ser7Leu, XP_011529749.1:p.Ser7Leu, XP_011529750.1:p.Ser7Leu, XP_011529753.1:p.Ser7Leu, XP_011529761.1:p.Ser7Leu, XP_011529762.1:p.Ser7Leu, XP_016885559.1:p.Ser7Leu, XP_016885560.1:p.Ser7Leu, XP_016885562.1:p.Ser7Leu, NP_001245178.1:p.Ser7Leu, XP_047298704.1:p.Ser7Leu, XP_047298705.1:p.Ser7Leu, XP_047298707.1:p.Ser7Leu, XP_047298708.1:p.Ser7Leu, XP_047298710.1:p.Ser7Leu, XP_047298703.1:p.Ser7Leu, XP_047298706.1:p.Ser7Leu, NP_001245187.1:p.Ser7Leu, NP_001245181.1:p.Ser7Leu, NP_001245190.1:p.Ser7Leu, NP_001245189.1:p.Ser7Leu, NP_001245193.1:p.Ser7Leu, NP_001245195.1:p.Ser7Leu, XP_047298709.1:p.Ser7Leu, NP_001245180.1:p.Ser7Leu, NP_001245196.1:p.Ser7Leu, NP_001245185.1:p.Ser7Leu, NP_001245188.1:p.Ser7Leu, NP_001245191.1:p.Ser7Leu, NP_001245182.1:p.Ser7Leu, NP_001245198.1:p.Ser7Leu, NP_001245192.1:p.Ser7Leu, NP_001245197.1:p.Ser7Leu, NP_001245184.1:p.Ser7Leu, NP_001245194.1:p.Ser7Leu, XP_047298702.1:p.Ser7Leu, NP_001245199.1:p.Ser7Leu, NP_001245186.1:p.Ser7Leu, NP_001245183.1:p.Ser7Leu, NP_001387106.1:p.Ser7Leu, NP_001245179.1:p.Ser7Leu, NP_001387104.1:p.Ser7Leu, NP_001387107.1:p.Ser7Leu, NP_001387110.1:p.Ser7Leu, NP_001387099.1:p.Ser7Leu, NP_001387100.1:p.Ser7Leu, NP_001387102.1:p.Ser7Leu, XP_047298711.1:p.Ser7Leu, NP_872600.1:p.Ser7Leu, XP_047298712.1:p.Ser7Leu, XP_047298713.1:p.Ser7Leu, NP_872601.1:p.Ser7Leu, NP_001387112.1:p.Ser7Leu, NP_001387114.1:p.Ser7Leu, NP_001387116.1:p.Ser7Leu, NP_001387118.1:p.Ser7Leu, NP_001387121.1:p.Ser7Leu, NP_001387124.1:p.Ser7Leu, NP_001387128.1:p.Ser7Leu

    2.

    rs1488385173 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      Y:13323621 (GRCh38)
      Y:15435501 (GRCh37)
      Canonical SPDI:
      NC_000024.10:13323620:A:G
      Gene:
      UTY (Varview)
      Functional Consequence:
      coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
      Validated:
      by frequency
      MAF:
      G=0.00001/1 (GnomAD_exomes)
      HGVS:
      NC_000024.10:g.13323621A>G, NC_000024.9:g.15435501A>G, XM_011531455.4:c.3258T>C, XM_011531455.3:c.3258T>C, XM_011531455.2:c.3258T>C, XM_011531455.1:c.3258T>C, XM_011531453.4:c.3258T>C, XM_011531453.3:c.3258T>C, XM_011531453.2:c.3258T>C, XM_011531453.1:c.3258T>C, XM_011531454.4:c.3258T>C, XM_011531454.3:c.3258T>C, XM_011531454.2:c.3258T>C, XM_011531454.1:c.3258T>C, NM_007125.4:c.2919T>C, XM_011531441.4:c.3258T>C, XM_011531441.3:c.3258T>C, XM_011531441.2:c.3258T>C, XM_011531441.1:c.3258T>C, XM_011531442.4:c.3210T>C, XM_011531442.3:c.3210T>C, XM_011531442.2:c.3210T>C, XM_011531442.1:c.3210T>C, XM_011531443.4:c.3192T>C, XM_011531443.3:c.3192T>C, XM_011531443.2:c.3192T>C, XM_011531443.1:c.3192T>C, XM_011531445.4:c.3123T>C, XM_011531445.3:c.3123T>C, XM_011531445.2:c.3123T>C, XM_011531445.1:c.3123T>C, XM_011531446.4:c.3102T>C, XM_011531446.3:c.3102T>C, XM_011531446.2:c.3102T>C, XM_011531446.1:c.3102T>C, XM_011531447.4:c.3075T>C, XM_011531447.3:c.3075T>C, XM_011531447.2:c.3075T>C, XM_011531447.1:c.3075T>C, XM_011531448.4:c.3057T>C, XM_011531448.3:c.3057T>C, XM_011531448.2:c.3057T>C, XM_011531448.1:c.3057T>C, XM_011531451.4:c.2967T>C, XM_011531451.3:c.2967T>C, XM_011531451.2:c.2967T>C, XM_011531451.1:c.2967T>C, XM_011531459.4:c.3258T>C, XM_011531459.3:c.3258T>C, XM_011531459.2:c.3258T>C, XM_011531459.1:c.3258T>C, XM_011531460.4:c.3258T>C, XM_011531460.3:c.3258T>C, XM_011531460.2:c.3258T>C, XM_011531460.1:c.3258T>C, XM_017030070.3:c.3258T>C, XM_017030070.2:c.3258T>C, XM_017030070.1:c.3258T>C, XM_017030071.3:c.3258T>C, XM_017030071.2:c.3258T>C, XM_017030071.1:c.3258T>C, XM_017030073.3:c.2967T>C, XM_017030073.2:c.2967T>C, XM_017030073.1:c.2967T>C, NM_001258249.2:c.3210T>C, NM_001258249.1:c.3210T>C, XM_047442748.1:c.3210T>C, XM_047442749.1:c.3144T>C, XM_047442751.1:c.3102T>C, XM_047442752.1:c.3075T>C, XM_047442754.1:c.3054T>C, NR_047607.1:n.4270T>C, NR_047598.1:n.4160T>C, NR_047624.1:n.4144T>C, XM_047442747.1:c.3210T>C, NR_047645.1:n.4130T>C, XM_047442750.1:c.3123T>C, NR_047644.1:n.4117T>C, NM_001258258.1:c.3075T>C, NR_047599.1:n.4047T>C, NM_001258252.1:c.3054T>C, NM_001258261.1:c.3045T>C, NR_047603.1:n.4047T>C, NR_047597.1:n.4030T>C, NR_047642.1:n.3924T>C, NR_047618.1:n.3933T>C, NM_001258260.1:c.3009T>C, NM_001258264.1:c.3006T>C, NR_047637.1:n.3982T>C, NR_047641.1:n.3924T>C, NM_001258266.1:c.3054T>C, XM_047442753.1:c.3054T>C, NM_001258251.1:c.2967T>C, NM_001258267.1:c.2919T>C, NR_047602.1:n.3889T>C, NM_001258256.1:c.3054T>C, NR_047647.1:n.3881T>C, NM_001258259.1:c.2871T>C, NR_047600.1:n.3848T>C, NM_001258262.1:c.2838T>C, NR_047638.1:n.3990T>C, NM_001258253.1:c.2967T>C, NR_047646.1:n.3797T>C, NM_001258269.1:c.2772T>C, NM_001258263.1:c.2919T>C, NR_047635.1:n.3919T>C, NM_001258268.1:c.2682T>C, NR_047632.1:n.3632T>C, NM_001258255.1:c.2682T>C, NR_047609.1:n.3682T>C, NM_001258265.1:c.2670T>C, XM_047442746.1:c.3144T>C, NM_001258270.1:c.2547T>C, NM_001258257.1:c.2547T>C, NR_047643.1:n.3524T>C, NM_001258254.1:c.2682T>C, NM_001400177.1:c.3144T>C, NM_001258250.1:c.2499T>C, NR_047612.1:n.3442T>C, NM_001400175.1:c.3144T>C, NM_001400178.1:c.3054T>C, NR_047614.1:n.3355T>C, NR_047629.1:n.3151T>C, NR_047621.1:n.3391T>C, NR_047623.1:n.3286T>C, NR_047601.1:n.3524T>C, NR_047622.1:n.3343T>C, NR_047617.1:n.3291T>C, NR_047608.1:n.3238T>C, NR_047615.1:n.3209T>C, NR_047636.1:n.3289T>C, NR_047606.1:n.3287T>C, NR_047611.1:n.3286T>C, NR_047631.1:n.3151T>C, NR_047610.1:n.3151T>C, NR_047628.1:n.3199T>C, NM_001400181.1:c.2919T>C, NR_047605.1:n.3103T>C, NR_047613.1:n.3392T>C, NR_047616.1:n.3265T>C, NR_047633.1:n.3200T>C, NR_047627.1:n.3354T>C, NR_047626.1:n.3151T>C, NR_047596.1:n.3151T>C, NR_047634.1:n.3150T>C, NR_047640.1:n.3135T>C, NR_047620.1:n.3286T>C, NR_047630.1:n.3151T>C, NR_047639.1:n.3057T>C, NR_047625.1:n.3024T>C, NR_047619.1:n.3209T>C, NR_047604.1:n.3017T>C, NM_001400170.1:c.3054T>C, NM_001400171.1:c.3009T>C, NM_001400173.1:c.2919T>C, XM_047442755.1:c.3210T>C, NM_182659.1:c.2919T>C, XR_007068451.1:n.4263T>C, XM_047442756.1:c.3054T>C, XR_007068452.1:n.4215T>C, NR_174404.1:n.2670T>C, XM_047442757.1:c.3192T>C, NR_174405.1:n.3287T>C, NM_182660.1:c.2919T>C, NM_001400183.1:c.3210T>C, NM_001400185.1:c.3144T>C, NM_001400187.1:c.3102T>C, NM_001400189.1:c.3057T>C, NM_001400192.1:c.3054T>C, NM_001400195.1:c.3009T>C, NM_001400199.1:c.2967T>C

      3.

      rs1486942920 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>G [Show Flanks]
        Chromosome:
        Y:13251020 (GRCh38)
        Y:15362900 (GRCh37)
        Canonical SPDI:
        NC_000024.10:13251019:T:G
        Gene:
        UTY (Varview)
        Functional Consequence:
        coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant,intron_variant,non_coding_transcript_variant
        Validated:
        by frequency
        MAF:
        G=0.00003/2 (GnomAD_exomes)
        HGVS:
        NC_000024.10:g.13251020T>G, NC_000024.9:g.15362900T>G, XM_011531455.4:c.4353A>C, XM_011531455.3:c.4353A>C, XM_011531455.2:c.4353A>C, XM_011531455.1:c.4353A>C, XM_011531453.4:c.4353A>C, XM_011531453.3:c.4353A>C, XM_011531453.2:c.4353A>C, XM_011531453.1:c.4353A>C, XM_011531454.4:c.4353A>C, XM_011531454.3:c.4353A>C, XM_011531454.2:c.4353A>C, XM_011531454.1:c.4353A>C, NM_007125.4:c.4014A>C, XM_011531441.4:c.4353A>C, XM_011531441.3:c.4353A>C, XM_011531441.2:c.4353A>C, XM_011531441.1:c.4353A>C, XM_011531442.4:c.4305A>C, XM_011531442.3:c.4305A>C, XM_011531442.2:c.4305A>C, XM_011531442.1:c.4305A>C, XM_011531443.4:c.4287A>C, XM_011531443.3:c.4287A>C, XM_011531443.2:c.4287A>C, XM_011531443.1:c.4287A>C, XM_011531445.4:c.4218A>C, XM_011531445.3:c.4218A>C, XM_011531445.2:c.4218A>C, XM_011531445.1:c.4218A>C, XM_011531446.4:c.4197A>C, XM_011531446.3:c.4197A>C, XM_011531446.2:c.4197A>C, XM_011531446.1:c.4197A>C, XM_011531447.4:c.4170A>C, XM_011531447.3:c.4170A>C, XM_011531447.2:c.4170A>C, XM_011531447.1:c.4170A>C, XM_011531448.4:c.4152A>C, XM_011531448.3:c.4152A>C, XM_011531448.2:c.4152A>C, XM_011531448.1:c.4152A>C, XM_011531451.4:c.4062A>C, XM_011531451.3:c.4062A>C, XM_011531451.2:c.4062A>C, XM_011531451.1:c.4062A>C, NM_001258249.2:c.4305A>C, NM_001258249.1:c.4305A>C, XM_047442748.1:c.4305A>C, XM_047442749.1:c.4239A>C, XM_047442751.1:c.4197A>C, XM_047442752.1:c.4170A>C, XM_047442754.1:c.4149A>C, NR_047607.1:n.5365A>C, NR_047598.1:n.5323A>C, NR_047624.1:n.5239A>C, XM_047442747.1:c.4305A>C, NR_047645.1:n.5225A>C, XM_047442750.1:c.4218A>C, NR_047644.1:n.5212A>C, NM_001258258.1:c.4170A>C, NR_047599.1:n.5142A>C, NM_001258252.1:c.4149A>C, NM_001258261.1:c.4140A>C, NR_047603.1:n.5142A>C, NR_047597.1:n.5125A>C, NR_047642.1:n.5124A>C, NR_047618.1:n.5120A>C, NM_001258260.1:c.4104A>C, NM_001258264.1:c.4101A>C, NR_047637.1:n.5077A>C, NR_047641.1:n.5087A>C, NM_001258266.1:c.4074A>C, XM_047442753.1:c.4149A>C, NM_001258251.1:c.4062A>C, NM_001258267.1:c.4014A>C, NR_047602.1:n.4984A>C, NR_047647.1:n.4976A>C, NM_001258259.1:c.3966A>C, NR_047600.1:n.4943A>C, NM_001258262.1:c.3933A>C, NR_047646.1:n.4892A>C, NM_001258269.1:c.3867A>C, NM_001258268.1:c.3777A>C, NR_047632.1:n.4795A>C, NM_001258255.1:c.3777A>C, NR_047609.1:n.4777A>C, NM_001258265.1:c.3765A>C, XM_047442746.1:c.4239A>C, NM_001258270.1:c.3642A>C, NM_001258257.1:c.3642A>C, NR_047643.1:n.4619A>C, NM_001400177.1:c.4239A>C, NM_001258250.1:c.3594A>C, NR_047612.1:n.4537A>C, NM_001400175.1:c.4239A>C, NM_001400178.1:c.4149A>C, NR_047614.1:n.4518A>C, NR_047629.1:n.4513A>C, NR_047621.1:n.4486A>C, NR_047623.1:n.4449A>C, NR_047622.1:n.4438A>C, NR_047617.1:n.4415A>C, NR_047608.1:n.4401A>C, NR_047615.1:n.4372A>C, NR_047636.1:n.4384A>C, NR_047606.1:n.4382A>C, NR_047611.1:n.4381A>C, NR_047631.1:n.4338A>C, NR_047610.1:n.4314A>C, NR_047628.1:n.4294A>C, NM_001400181.1:c.4014A>C, NR_047605.1:n.4303A>C, NR_047613.1:n.4299A>C, NR_047616.1:n.4298A>C, NR_047633.1:n.4295A>C, NR_047627.1:n.4261A>C, NR_047626.1:n.4246A>C, NR_047596.1:n.4246A>C, NR_047634.1:n.4245A>C, NR_047640.1:n.4230A>C, NR_047630.1:n.4171A>C, NR_047639.1:n.4152A>C, NR_047625.1:n.4119A>C, NR_047604.1:n.4112A>C, NM_001400170.1:c.4149A>C, NM_001400171.1:c.4104A>C, NM_001400173.1:c.4014A>C, NR_174404.1:n.3765A>C

        4.

        rs1486115496 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>G [Show Flanks]
          Chromosome:
          Y:13479551 (GRCh38)
          Y:15591431 (GRCh37)
          Canonical SPDI:
          NC_000024.10:13479550:T:G
          Gene:
          UTY (Varview), MIR12120 (Varview)
          Functional Consequence:
          coding_sequence_variant,missense_variant,500B_downstream_variant,non_coding_transcript_variant,downstream_transcript_variant
          Validated:
          by frequency
          MAF:
          G=0.00001/1 (GnomAD_exomes)
          HGVS:
          NC_000024.10:g.13479551T>G, NC_000024.9:g.15591431T>G, XM_011531455.4:c.115A>C, XM_011531455.3:c.115A>C, XM_011531455.2:c.115A>C, XM_011531455.1:c.115A>C, XM_011531453.4:c.115A>C, XM_011531453.3:c.115A>C, XM_011531453.2:c.115A>C, XM_011531453.1:c.115A>C, XM_011531454.4:c.115A>C, XM_011531454.3:c.115A>C, XM_011531454.2:c.115A>C, XM_011531454.1:c.115A>C, NM_007125.4:c.115A>C, XM_011531441.4:c.115A>C, XM_011531441.3:c.115A>C, XM_011531441.2:c.115A>C, XM_011531441.1:c.115A>C, XM_011531442.4:c.115A>C, XM_011531442.3:c.115A>C, XM_011531442.2:c.115A>C, XM_011531442.1:c.115A>C, XM_011531443.4:c.115A>C, XM_011531443.3:c.115A>C, XM_011531443.2:c.115A>C, XM_011531443.1:c.115A>C, XM_011531445.4:c.115A>C, XM_011531445.3:c.115A>C, XM_011531445.2:c.115A>C, XM_011531445.1:c.115A>C, XM_011531446.4:c.115A>C, XM_011531446.3:c.115A>C, XM_011531446.2:c.115A>C, XM_011531446.1:c.115A>C, XM_011531447.4:c.115A>C, XM_011531447.3:c.115A>C, XM_011531447.2:c.115A>C, XM_011531447.1:c.115A>C, XM_011531448.4:c.115A>C, XM_011531448.3:c.115A>C, XM_011531448.2:c.115A>C, XM_011531448.1:c.115A>C, XM_011531451.4:c.115A>C, XM_011531451.3:c.115A>C, XM_011531451.2:c.115A>C, XM_011531451.1:c.115A>C, XM_011531459.4:c.115A>C, XM_011531459.3:c.115A>C, XM_011531459.2:c.115A>C, XM_011531459.1:c.115A>C, XM_011531460.4:c.115A>C, XM_011531460.3:c.115A>C, XM_011531460.2:c.115A>C, XM_011531460.1:c.115A>C, XM_017030070.3:c.115A>C, XM_017030070.2:c.115A>C, XM_017030070.1:c.115A>C, XM_017030071.3:c.115A>C, XM_017030071.2:c.115A>C, XM_017030071.1:c.115A>C, XM_017030073.3:c.115A>C, XM_017030073.2:c.115A>C, XM_017030073.1:c.115A>C, NM_001258249.2:c.115A>C, NM_001258249.1:c.115A>C, XM_047442748.1:c.115A>C, XM_047442749.1:c.115A>C, XM_047442751.1:c.115A>C, XM_047442752.1:c.115A>C, XM_047442754.1:c.115A>C, NR_047607.1:n.1120A>C, NR_047598.1:n.1120A>C, NR_047624.1:n.1120A>C, XM_047442747.1:c.115A>C, NR_047645.1:n.1120A>C, XM_047442750.1:c.115A>C, NR_047644.1:n.1120A>C, NM_001258258.1:c.115A>C, NR_047599.1:n.1120A>C, NM_001258252.1:c.115A>C, NM_001258261.1:c.115A>C, NR_047603.1:n.1120A>C, NR_047597.1:n.1120A>C, NR_047642.1:n.1120A>C, NR_047618.1:n.1120A>C, NM_001258260.1:c.115A>C, NM_001258264.1:c.115A>C, NR_047637.1:n.1120A>C, NR_047641.1:n.1120A>C, NM_001258266.1:c.115A>C, XM_047442753.1:c.115A>C, NM_001258251.1:c.115A>C, NM_001258267.1:c.115A>C, NR_047602.1:n.1120A>C, NM_001258256.1:c.115A>C, NR_047647.1:n.1120A>C, NM_001258259.1:c.115A>C, NR_047600.1:n.1120A>C, NM_001258262.1:c.115A>C, NR_047638.1:n.1120A>C, NM_001258253.1:c.115A>C, NR_047646.1:n.1120A>C, NM_001258269.1:c.115A>C, NM_001258263.1:c.115A>C, NR_047635.1:n.1120A>C, NM_001258268.1:c.115A>C, NR_047632.1:n.1120A>C, NM_001258255.1:c.115A>C, NR_047609.1:n.1120A>C, NM_001258265.1:c.115A>C, XM_047442746.1:c.115A>C, NM_001258270.1:c.115A>C, NM_001258257.1:c.115A>C, NR_047643.1:n.1120A>C, NM_001258254.1:c.115A>C, NM_001400177.1:c.115A>C, NM_001258250.1:c.115A>C, NR_047612.1:n.1120A>C, NM_001400175.1:c.115A>C, NM_001400178.1:c.115A>C, NR_047614.1:n.1120A>C, NR_047629.1:n.1120A>C, NR_047621.1:n.1120A>C, NR_047623.1:n.1120A>C, NR_047601.1:n.1120A>C, NR_047622.1:n.1120A>C, NR_047617.1:n.1120A>C, NR_047608.1:n.1120A>C, NR_047615.1:n.1120A>C, NR_047636.1:n.1120A>C, NR_047606.1:n.1120A>C, NR_047611.1:n.1120A>C, NR_047631.1:n.1120A>C, NR_047610.1:n.1120A>C, NR_047628.1:n.1120A>C, NM_001400181.1:c.115A>C, NR_047605.1:n.1120A>C, NR_047613.1:n.1120A>C, NR_047616.1:n.1120A>C, NR_047633.1:n.1120A>C, NR_047627.1:n.1120A>C, NR_047626.1:n.1120A>C, NR_047596.1:n.1120A>C, NR_047634.1:n.1120A>C, NR_047640.1:n.1120A>C, NR_047620.1:n.1120A>C, NR_047630.1:n.1120A>C, NR_047639.1:n.1120A>C, NR_047625.1:n.1120A>C, NR_047619.1:n.1120A>C, NR_047604.1:n.1120A>C, NM_001400170.1:c.115A>C, NM_001400171.1:c.115A>C, NM_001400173.1:c.115A>C, XM_047442755.1:c.115A>C, NM_182659.1:c.115A>C, XR_007068451.1:n.1120A>C, XM_047442756.1:c.115A>C, XR_007068452.1:n.1120A>C, NR_174404.1:n.483A>C, XM_047442757.1:c.115A>C, NR_174405.1:n.483A>C, NM_182660.1:c.115A>C, NM_001400183.1:c.115A>C, NM_001400185.1:c.115A>C, NM_001400187.1:c.115A>C, NM_001400189.1:c.115A>C, NM_001400192.1:c.115A>C, NM_001400195.1:c.115A>C, NM_001400199.1:c.115A>C, XP_011529757.1:p.Thr39Pro, XP_011529755.1:p.Thr39Pro, XP_011529756.1:p.Thr39Pro, NP_009056.3:p.Thr39Pro, XP_011529743.1:p.Thr39Pro, XP_011529744.1:p.Thr39Pro, XP_011529745.1:p.Thr39Pro, XP_011529747.1:p.Thr39Pro, XP_011529748.1:p.Thr39Pro, XP_011529749.1:p.Thr39Pro, XP_011529750.1:p.Thr39Pro, XP_011529753.1:p.Thr39Pro, XP_011529761.1:p.Thr39Pro, XP_011529762.1:p.Thr39Pro, XP_016885559.1:p.Thr39Pro, XP_016885560.1:p.Thr39Pro, XP_016885562.1:p.Thr39Pro, NP_001245178.1:p.Thr39Pro, XP_047298704.1:p.Thr39Pro, XP_047298705.1:p.Thr39Pro, XP_047298707.1:p.Thr39Pro, XP_047298708.1:p.Thr39Pro, XP_047298710.1:p.Thr39Pro, XP_047298703.1:p.Thr39Pro, XP_047298706.1:p.Thr39Pro, NP_001245187.1:p.Thr39Pro, NP_001245181.1:p.Thr39Pro, NP_001245190.1:p.Thr39Pro, NP_001245189.1:p.Thr39Pro, NP_001245193.1:p.Thr39Pro, NP_001245195.1:p.Thr39Pro, XP_047298709.1:p.Thr39Pro, NP_001245180.1:p.Thr39Pro, NP_001245196.1:p.Thr39Pro, NP_001245185.1:p.Thr39Pro, NP_001245188.1:p.Thr39Pro, NP_001245191.1:p.Thr39Pro, NP_001245182.1:p.Thr39Pro, NP_001245198.1:p.Thr39Pro, NP_001245192.1:p.Thr39Pro, NP_001245197.1:p.Thr39Pro, NP_001245184.1:p.Thr39Pro, NP_001245194.1:p.Thr39Pro, XP_047298702.1:p.Thr39Pro, NP_001245199.1:p.Thr39Pro, NP_001245186.1:p.Thr39Pro, NP_001245183.1:p.Thr39Pro, NP_001387106.1:p.Thr39Pro, NP_001245179.1:p.Thr39Pro, NP_001387104.1:p.Thr39Pro, NP_001387107.1:p.Thr39Pro, NP_001387110.1:p.Thr39Pro, NP_001387099.1:p.Thr39Pro, NP_001387100.1:p.Thr39Pro, NP_001387102.1:p.Thr39Pro, XP_047298711.1:p.Thr39Pro, NP_872600.1:p.Thr39Pro, XP_047298712.1:p.Thr39Pro, XP_047298713.1:p.Thr39Pro, NP_872601.1:p.Thr39Pro, NP_001387112.1:p.Thr39Pro, NP_001387114.1:p.Thr39Pro, NP_001387116.1:p.Thr39Pro, NP_001387118.1:p.Thr39Pro, NP_001387121.1:p.Thr39Pro, NP_001387124.1:p.Thr39Pro, NP_001387128.1:p.Thr39Pro

          5.

          rs1483775547 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A [Show Flanks]
            Chromosome:
            Y:13355641 (GRCh38)
            Y:15467521 (GRCh37)
            Canonical SPDI:
            NC_000024.10:13355640:C:A
            Gene:
            UTY (Varview)
            Functional Consequence:
            intron_variant,non_coding_transcript_variant
            Validated:
            by frequency,by cluster
            MAF:
            A=0.00007/2 (GnomAD)
            A=0.00008/2 (GnomAD_exomes)
            HGVS:

            6.

            rs1482791252 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>G [Show Flanks]
              Chromosome:
              Y:13336324 (GRCh38)
              Y:15448204 (GRCh37)
              Canonical SPDI:
              NC_000024.10:13336323:T:G
              Gene:
              UTY (Varview)
              Functional Consequence:
              missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant
              Validated:
              by frequency
              MAF:
              G=0.00002/1 (GnomAD_exomes)
              HGVS:
              NC_000024.10:g.13336324T>G, NC_000024.9:g.15448204T>G, XM_011531455.4:c.2121A>C, XM_011531455.3:c.2121A>C, XM_011531455.2:c.2121A>C, XM_011531455.1:c.2121A>C, XM_011531453.4:c.2121A>C, XM_011531453.3:c.2121A>C, XM_011531453.2:c.2121A>C, XM_011531453.1:c.2121A>C, XM_011531454.4:c.2121A>C, XM_011531454.3:c.2121A>C, XM_011531454.2:c.2121A>C, XM_011531454.1:c.2121A>C, NM_007125.4:c.1782A>C, XM_011531441.4:c.2121A>C, XM_011531441.3:c.2121A>C, XM_011531441.2:c.2121A>C, XM_011531441.1:c.2121A>C, XM_011531442.4:c.2073A>C, XM_011531442.3:c.2073A>C, XM_011531442.2:c.2073A>C, XM_011531442.1:c.2073A>C, XM_011531443.4:c.2055A>C, XM_011531443.3:c.2055A>C, XM_011531443.2:c.2055A>C, XM_011531443.1:c.2055A>C, XM_011531445.4:c.1986A>C, XM_011531445.3:c.1986A>C, XM_011531445.2:c.1986A>C, XM_011531445.1:c.1986A>C, XM_011531446.4:c.1965A>C, XM_011531446.3:c.1965A>C, XM_011531446.2:c.1965A>C, XM_011531446.1:c.1965A>C, XM_011531447.4:c.1938A>C, XM_011531447.3:c.1938A>C, XM_011531447.2:c.1938A>C, XM_011531447.1:c.1938A>C, XM_011531448.4:c.1920A>C, XM_011531448.3:c.1920A>C, XM_011531448.2:c.1920A>C, XM_011531448.1:c.1920A>C, XM_011531451.4:c.1830A>C, XM_011531451.3:c.1830A>C, XM_011531451.2:c.1830A>C, XM_011531451.1:c.1830A>C, XM_011531459.4:c.2121A>C, XM_011531459.3:c.2121A>C, XM_011531459.2:c.2121A>C, XM_011531459.1:c.2121A>C, XM_011531460.4:c.2121A>C, XM_011531460.3:c.2121A>C, XM_011531460.2:c.2121A>C, XM_011531460.1:c.2121A>C, XM_017030070.3:c.2121A>C, XM_017030070.2:c.2121A>C, XM_017030070.1:c.2121A>C, XM_017030071.3:c.2121A>C, XM_017030071.2:c.2121A>C, XM_017030071.1:c.2121A>C, XM_017030073.3:c.1830A>C, XM_017030073.2:c.1830A>C, XM_017030073.1:c.1830A>C, NM_001258249.2:c.2073A>C, NM_001258249.1:c.2073A>C, XM_047442748.1:c.2073A>C, XM_047442749.1:c.2007A>C, XM_047442751.1:c.1965A>C, XM_047442752.1:c.1938A>C, XM_047442754.1:c.1917A>C, NR_047607.1:n.3133A>C, NR_047598.1:n.3023A>C, NR_047624.1:n.3007A>C, XM_047442747.1:c.2073A>C, NR_047645.1:n.2993A>C, XM_047442750.1:c.1986A>C, NR_047644.1:n.2980A>C, NM_001258258.1:c.1938A>C, NR_047599.1:n.2787A>C, NM_001258252.1:c.1917A>C, NM_001258261.1:c.1908A>C, NR_047603.1:n.2910A>C, NR_047597.1:n.2893A>C, NR_047642.1:n.2787A>C, NR_047618.1:n.2796A>C, NM_001258260.1:c.1872A>C, NM_001258264.1:c.1869A>C, NR_047637.1:n.2845A>C, NR_047641.1:n.2787A>C, NM_001258266.1:c.1917A>C, XM_047442753.1:c.1917A>C, NM_001258251.1:c.1830A>C, NM_001258267.1:c.1782A>C, NR_047602.1:n.2752A>C, NM_001258256.1:c.1917A>C, NR_047647.1:n.2744A>C, NM_001258259.1:c.1734A>C, NR_047600.1:n.2711A>C, NM_001258262.1:c.1701A>C, NR_047638.1:n.2853A>C, NM_001258253.1:c.1830A>C, NR_047646.1:n.2660A>C, NM_001258269.1:c.1635A>C, NM_001258263.1:c.1782A>C, NR_047635.1:n.2782A>C, NM_001258268.1:c.1545A>C, NR_047632.1:n.2495A>C, NM_001258255.1:c.1545A>C, NR_047609.1:n.2545A>C, NM_001258265.1:c.1533A>C, XM_047442746.1:c.2007A>C, NM_001258270.1:c.1410A>C, NM_001258257.1:c.1410A>C, NM_001258254.1:c.1545A>C, NM_001400177.1:c.2007A>C, NM_001258250.1:c.1362A>C, NM_001400175.1:c.2007A>C, NM_001400178.1:c.1917A>C, NM_001400181.1:c.1782A>C, NM_001400170.1:c.1917A>C, NM_001400171.1:c.1872A>C, NM_001400173.1:c.1782A>C, XM_047442755.1:c.2073A>C, NM_182659.1:c.1782A>C, XR_007068451.1:n.3126A>C, XM_047442756.1:c.1917A>C, XR_007068452.1:n.3078A>C, XM_047442757.1:c.2055A>C, NR_174405.1:n.2150A>C, NM_182660.1:c.1782A>C, NM_001400183.1:c.2073A>C, NM_001400185.1:c.2007A>C, NM_001400187.1:c.1965A>C, NM_001400189.1:c.1920A>C, NM_001400192.1:c.1917A>C, NM_001400195.1:c.1872A>C, NM_001400199.1:c.1830A>C, XP_011529757.1:p.Lys707Asn, XP_011529755.1:p.Lys707Asn, XP_011529756.1:p.Lys707Asn, NP_009056.3:p.Lys594Asn, XP_011529743.1:p.Lys707Asn, XP_011529744.1:p.Lys691Asn, XP_011529745.1:p.Lys685Asn, XP_011529747.1:p.Lys662Asn, XP_011529748.1:p.Lys655Asn, XP_011529749.1:p.Lys646Asn, XP_011529750.1:p.Lys640Asn, XP_011529753.1:p.Lys610Asn, XP_011529761.1:p.Lys707Asn, XP_011529762.1:p.Lys707Asn, XP_016885559.1:p.Lys707Asn, XP_016885560.1:p.Lys707Asn, XP_016885562.1:p.Lys610Asn, NP_001245178.1:p.Lys691Asn, XP_047298704.1:p.Lys691Asn, XP_047298705.1:p.Lys669Asn, XP_047298707.1:p.Lys655Asn, XP_047298708.1:p.Lys646Asn, XP_047298710.1:p.Lys639Asn, XP_047298703.1:p.Lys691Asn, XP_047298706.1:p.Lys662Asn, NP_001245187.1:p.Lys646Asn, NP_001245181.1:p.Lys639Asn, NP_001245190.1:p.Lys636Asn, NP_001245189.1:p.Lys624Asn, NP_001245193.1:p.Lys623Asn, NP_001245195.1:p.Lys639Asn, XP_047298709.1:p.Lys639Asn, NP_001245180.1:p.Lys610Asn, NP_001245196.1:p.Lys594Asn, NP_001245185.1:p.Lys639Asn, NP_001245188.1:p.Lys578Asn, NP_001245191.1:p.Lys567Asn, NP_001245182.1:p.Lys610Asn, NP_001245198.1:p.Lys545Asn, NP_001245192.1:p.Lys594Asn, NP_001245197.1:p.Lys515Asn, NP_001245184.1:p.Lys515Asn, NP_001245194.1:p.Lys511Asn, XP_047298702.1:p.Lys669Asn, NP_001245199.1:p.Lys470Asn, NP_001245186.1:p.Lys470Asn, NP_001245183.1:p.Lys515Asn, NP_001387106.1:p.Lys669Asn, NP_001245179.1:p.Lys454Asn, NP_001387104.1:p.Lys669Asn, NP_001387107.1:p.Lys639Asn, NP_001387110.1:p.Lys594Asn, NP_001387099.1:p.Lys639Asn, NP_001387100.1:p.Lys624Asn, NP_001387102.1:p.Lys594Asn, XP_047298711.1:p.Lys691Asn, NP_872600.1:p.Lys594Asn, XP_047298712.1:p.Lys639Asn, XP_047298713.1:p.Lys685Asn, NP_872601.1:p.Lys594Asn, NP_001387112.1:p.Lys691Asn, NP_001387114.1:p.Lys669Asn, NP_001387116.1:p.Lys655Asn, NP_001387118.1:p.Lys640Asn, NP_001387121.1:p.Lys639Asn, NP_001387124.1:p.Lys624Asn, NP_001387128.1:p.Lys610Asn

              7.

              rs1477017763 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                Y:13297749 (GRCh38)
                Y:15409629 (GRCh37)
                Canonical SPDI:
                NC_000024.10:13297748:C:T
                Gene:
                UTY (Varview)
                Functional Consequence:
                3_prime_UTR_variant,coding_sequence_variant,genic_downstream_transcript_variant,missense_variant,non_coding_transcript_variant
                Validated:
                by frequency
                MAF:
                T=0.00001/1 (GnomAD_exomes)
                HGVS:
                NC_000024.10:g.13297749C>T, NC_000024.9:g.15409629C>T, XM_011531455.4:c.4016G>A, XM_011531455.3:c.4016G>A, XM_011531455.2:c.4016G>A, XM_011531455.1:c.4016G>A, XM_011531453.4:c.4016G>A, XM_011531453.3:c.4016G>A, XM_011531453.2:c.4016G>A, XM_011531453.1:c.4016G>A, XM_011531454.4:c.4016G>A, XM_011531454.3:c.4016G>A, XM_011531454.2:c.4016G>A, XM_011531454.1:c.4016G>A, NM_007125.4:c.3677G>A, XM_011531441.4:c.4016G>A, XM_011531441.3:c.4016G>A, XM_011531441.2:c.4016G>A, XM_011531441.1:c.4016G>A, XM_011531442.4:c.3968G>A, XM_011531442.3:c.3968G>A, XM_011531442.2:c.3968G>A, XM_011531442.1:c.3968G>A, XM_011531443.4:c.3950G>A, XM_011531443.3:c.3950G>A, XM_011531443.2:c.3950G>A, XM_011531443.1:c.3950G>A, XM_011531445.4:c.3881G>A, XM_011531445.3:c.3881G>A, XM_011531445.2:c.3881G>A, XM_011531445.1:c.3881G>A, XM_011531446.4:c.3860G>A, XM_011531446.3:c.3860G>A, XM_011531446.2:c.3860G>A, XM_011531446.1:c.3860G>A, XM_011531447.4:c.3833G>A, XM_011531447.3:c.3833G>A, XM_011531447.2:c.3833G>A, XM_011531447.1:c.3833G>A, XM_011531448.4:c.3815G>A, XM_011531448.3:c.3815G>A, XM_011531448.2:c.3815G>A, XM_011531448.1:c.3815G>A, XM_011531451.4:c.3725G>A, XM_011531451.3:c.3725G>A, XM_011531451.2:c.3725G>A, XM_011531451.1:c.3725G>A, XM_011531459.4:c.4016G>A, XM_011531459.3:c.4016G>A, XM_011531459.2:c.4016G>A, XM_011531459.1:c.4016G>A, XM_017030070.3:c.*87G>A, XM_017030070.2:c.*87G>A, XM_017030070.1:c.*87G>A, NM_001258249.2:c.3968G>A, NM_001258249.1:c.3968G>A, XM_047442748.1:c.3968G>A, XM_047442749.1:c.3902G>A, XM_047442751.1:c.3860G>A, XM_047442752.1:c.3833G>A, XM_047442754.1:c.3812G>A, NR_047607.1:n.5028G>A, NR_047598.1:n.4986G>A, NR_047624.1:n.4902G>A, XM_047442747.1:c.3968G>A, NR_047645.1:n.4888G>A, XM_047442750.1:c.3881G>A, NR_047644.1:n.4875G>A, NM_001258258.1:c.3833G>A, NR_047599.1:n.4805G>A, NM_001258252.1:c.3812G>A, NM_001258261.1:c.3803G>A, NR_047603.1:n.4805G>A, NR_047597.1:n.4788G>A, NR_047642.1:n.4682G>A, NR_047618.1:n.4783G>A, NM_001258260.1:c.3767G>A, NM_001258264.1:c.3764G>A, NR_047637.1:n.4740G>A, NR_047641.1:n.4750G>A, NM_001258266.1:c.3737G>A, XM_047442753.1:c.3812G>A, NM_001258251.1:c.3725G>A, NM_001258267.1:c.3677G>A, NR_047602.1:n.4647G>A, NM_001258256.1:c.3812G>A, NR_047647.1:n.4639G>A, NM_001258259.1:c.3629G>A, NR_047600.1:n.4606G>A, NM_001258262.1:c.3596G>A, NR_047638.1:n.4748G>A, NM_001258253.1:c.3725G>A, NR_047646.1:n.4555G>A, NM_001258269.1:c.3530G>A, NM_001258263.1:c.3677G>A, NR_047635.1:n.4677G>A, NM_001258268.1:c.3440G>A, NR_047632.1:n.4458G>A, NM_001258255.1:c.3440G>A, NR_047609.1:n.4440G>A, NM_001258265.1:c.3428G>A, XM_047442746.1:c.3902G>A, NM_001258270.1:c.3305G>A, NM_001258257.1:c.3305G>A, NR_047643.1:n.4282G>A, NM_001258254.1:c.3440G>A, NM_001400177.1:c.3902G>A, NM_001258250.1:c.3257G>A, NR_047612.1:n.4200G>A, NM_001400175.1:c.3902G>A, NM_001400178.1:c.3812G>A, NR_047614.1:n.4181G>A, NR_047629.1:n.4176G>A, NR_047621.1:n.4149G>A, NR_047623.1:n.4112G>A, NR_047601.1:n.4282G>A, NR_047622.1:n.4101G>A, NR_047617.1:n.4078G>A, NR_047608.1:n.4064G>A, NR_047615.1:n.4035G>A, NR_047636.1:n.4047G>A, NR_047606.1:n.4045G>A, NR_047611.1:n.4044G>A, NR_047631.1:n.4001G>A, NR_047610.1:n.3977G>A, NR_047628.1:n.3957G>A, NM_001400181.1:c.3677G>A, NR_047605.1:n.3861G>A, NR_047613.1:n.3962G>A, NR_047616.1:n.3961G>A, NR_047633.1:n.3958G>A, NR_047627.1:n.3924G>A, NR_047626.1:n.3909G>A, NR_047596.1:n.3909G>A, NR_047634.1:n.3908G>A, NR_047640.1:n.3893G>A, NR_047620.1:n.4044G>A, NR_047630.1:n.3834G>A, NR_047639.1:n.3815G>A, NR_047625.1:n.3782G>A, NR_047619.1:n.3967G>A, NR_047604.1:n.3775G>A, NM_001400170.1:c.3812G>A, NM_001400171.1:c.3767G>A, NM_001400173.1:c.3677G>A, XM_047442755.1:c.3968G>A, NM_182659.1:c.3677G>A, XM_047442756.1:c.*87G>A, NR_174404.1:n.3428G>A, NR_174405.1:n.4137G>A, XP_011529757.1:p.Arg1339Gln, XP_011529755.1:p.Arg1339Gln, XP_011529756.1:p.Arg1339Gln, NP_009056.3:p.Arg1226Gln, XP_011529743.1:p.Arg1339Gln, XP_011529744.1:p.Arg1323Gln, XP_011529745.1:p.Arg1317Gln, XP_011529747.1:p.Arg1294Gln, XP_011529748.1:p.Arg1287Gln, XP_011529749.1:p.Arg1278Gln, XP_011529750.1:p.Arg1272Gln, XP_011529753.1:p.Arg1242Gln, XP_011529761.1:p.Arg1339Gln, NP_001245178.1:p.Arg1323Gln, XP_047298704.1:p.Arg1323Gln, XP_047298705.1:p.Arg1301Gln, XP_047298707.1:p.Arg1287Gln, XP_047298708.1:p.Arg1278Gln, XP_047298710.1:p.Arg1271Gln, XP_047298703.1:p.Arg1323Gln, XP_047298706.1:p.Arg1294Gln, NP_001245187.1:p.Arg1278Gln, NP_001245181.1:p.Arg1271Gln, NP_001245190.1:p.Arg1268Gln, NP_001245189.1:p.Arg1256Gln, NP_001245193.1:p.Arg1255Gln, NP_001245195.1:p.Arg1246Gln, XP_047298709.1:p.Arg1271Gln, NP_001245180.1:p.Arg1242Gln, NP_001245196.1:p.Arg1226Gln, NP_001245185.1:p.Arg1271Gln, NP_001245188.1:p.Arg1210Gln, NP_001245191.1:p.Arg1199Gln, NP_001245182.1:p.Arg1242Gln, NP_001245198.1:p.Arg1177Gln, NP_001245192.1:p.Arg1226Gln, NP_001245197.1:p.Arg1147Gln, NP_001245184.1:p.Arg1147Gln, NP_001245194.1:p.Arg1143Gln, XP_047298702.1:p.Arg1301Gln, NP_001245199.1:p.Arg1102Gln, NP_001245186.1:p.Arg1102Gln, NP_001245183.1:p.Arg1147Gln, NP_001387106.1:p.Arg1301Gln, NP_001245179.1:p.Arg1086Gln, NP_001387104.1:p.Arg1301Gln, NP_001387107.1:p.Arg1271Gln, NP_001387110.1:p.Arg1226Gln, NP_001387099.1:p.Arg1271Gln, NP_001387100.1:p.Arg1256Gln, NP_001387102.1:p.Arg1226Gln, XP_047298711.1:p.Arg1323Gln, NP_872600.1:p.Arg1226Gln

                8.

                rs1476506511 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  Y:13305436 (GRCh38)
                  Y:15417316 (GRCh37)
                  Canonical SPDI:
                  NC_000024.10:13305435:T:C
                  Gene:
                  UTY (Varview)
                  Functional Consequence:
                  coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant,non_coding_transcript_variant,downstream_transcript_variant
                  Validated:
                  by frequency
                  MAF:
                  C=0.00002/1 (GnomAD_exomes)
                  HGVS:
                  NC_000024.10:g.13305436T>C, NC_000024.9:g.15417316T>C, XM_011531455.4:c.3576A>G, XM_011531455.3:c.3576A>G, XM_011531455.2:c.3576A>G, XM_011531455.1:c.3576A>G, XM_011531453.4:c.3576A>G, XM_011531453.3:c.3576A>G, XM_011531453.2:c.3576A>G, XM_011531453.1:c.3576A>G, XM_011531454.4:c.3576A>G, XM_011531454.3:c.3576A>G, XM_011531454.2:c.3576A>G, XM_011531454.1:c.3576A>G, NM_007125.4:c.3237A>G, XM_011531441.4:c.3576A>G, XM_011531441.3:c.3576A>G, XM_011531441.2:c.3576A>G, XM_011531441.1:c.3576A>G, XM_011531442.4:c.3528A>G, XM_011531442.3:c.3528A>G, XM_011531442.2:c.3528A>G, XM_011531442.1:c.3528A>G, XM_011531443.4:c.3510A>G, XM_011531443.3:c.3510A>G, XM_011531443.2:c.3510A>G, XM_011531443.1:c.3510A>G, XM_011531445.4:c.3441A>G, XM_011531445.3:c.3441A>G, XM_011531445.2:c.3441A>G, XM_011531445.1:c.3441A>G, XM_011531446.4:c.3420A>G, XM_011531446.3:c.3420A>G, XM_011531446.2:c.3420A>G, XM_011531446.1:c.3420A>G, XM_011531447.4:c.3393A>G, XM_011531447.3:c.3393A>G, XM_011531447.2:c.3393A>G, XM_011531447.1:c.3393A>G, XM_011531448.4:c.3375A>G, XM_011531448.3:c.3375A>G, XM_011531448.2:c.3375A>G, XM_011531448.1:c.3375A>G, XM_011531451.4:c.3285A>G, XM_011531451.3:c.3285A>G, XM_011531451.2:c.3285A>G, XM_011531451.1:c.3285A>G, XM_011531459.4:c.3576A>G, XM_011531459.3:c.3576A>G, XM_011531459.2:c.3576A>G, XM_011531459.1:c.3576A>G, XM_017030070.3:c.3576A>G, XM_017030070.2:c.3576A>G, XM_017030070.1:c.3576A>G, NM_001258249.2:c.3528A>G, NM_001258249.1:c.3528A>G, XM_047442748.1:c.3528A>G, XM_047442749.1:c.3462A>G, XM_047442751.1:c.3420A>G, XM_047442752.1:c.3393A>G, XM_047442754.1:c.3372A>G, NR_047607.1:n.4588A>G, NR_047598.1:n.4546A>G, NR_047624.1:n.4462A>G, XM_047442747.1:c.3528A>G, NR_047645.1:n.4448A>G, XM_047442750.1:c.3441A>G, NR_047644.1:n.4435A>G, NM_001258258.1:c.3393A>G, NR_047599.1:n.4365A>G, NM_001258252.1:c.3372A>G, NM_001258261.1:c.3363A>G, NR_047603.1:n.4365A>G, NR_047597.1:n.4348A>G, NR_047642.1:n.4242A>G, NR_047618.1:n.4251A>G, NM_001258260.1:c.3327A>G, NM_001258264.1:c.3324A>G, NR_047637.1:n.4300A>G, NR_047641.1:n.4310A>G, NM_001258266.1:c.3297A>G, XM_047442753.1:c.3372A>G, NM_001258251.1:c.3285A>G, NM_001258267.1:c.3237A>G, NR_047602.1:n.4207A>G, NM_001258256.1:c.3372A>G, NR_047647.1:n.4199A>G, NM_001258259.1:c.3189A>G, NR_047600.1:n.4166A>G, NM_001258262.1:c.3156A>G, NR_047638.1:n.4308A>G, NM_001258253.1:c.3285A>G, NR_047646.1:n.4115A>G, NM_001258269.1:c.3090A>G, NM_001258263.1:c.3237A>G, NR_047635.1:n.4237A>G, NM_001258268.1:c.3000A>G, NR_047632.1:n.3950A>G, NM_001258255.1:c.3000A>G, NR_047609.1:n.4000A>G, NM_001258265.1:c.2988A>G, XM_047442746.1:c.3462A>G, NM_001258270.1:c.2865A>G, NM_001258257.1:c.2865A>G, NR_047643.1:n.3842A>G, NM_001258254.1:c.3000A>G, NM_001400177.1:c.3462A>G, NM_001258250.1:c.2817A>G, NR_047612.1:n.3760A>G, NM_001400175.1:c.3462A>G, NM_001400178.1:c.3372A>G, NR_047614.1:n.3673A>G, NR_047629.1:n.3736A>G, NR_047621.1:n.3709A>G, NR_047623.1:n.3604A>G, NR_047601.1:n.3842A>G, NR_047622.1:n.3661A>G, NR_047617.1:n.3609A>G, NR_047608.1:n.3624A>G, NR_047615.1:n.3527A>G, NR_047636.1:n.3607A>G, NR_047606.1:n.3605A>G, NR_047611.1:n.3604A>G, NR_047631.1:n.3469A>G, NR_047610.1:n.3537A>G, NR_047628.1:n.3517A>G, NM_001400181.1:c.3237A>G, NR_047605.1:n.3421A>G, NR_047613.1:n.3710A>G, NR_047616.1:n.3521A>G, NR_047633.1:n.3518A>G, NR_047627.1:n.3672A>G, NR_047626.1:n.3469A>G, NR_047596.1:n.3469A>G, NR_047634.1:n.3468A>G, NR_047640.1:n.3453A>G, NR_047620.1:n.3604A>G, NR_047630.1:n.3394A>G, NR_047639.1:n.3375A>G, NR_047625.1:n.3342A>G, NR_047619.1:n.3527A>G, NR_047604.1:n.3335A>G, NM_001400170.1:c.3372A>G, NM_001400171.1:c.3327A>G, NM_001400173.1:c.3237A>G, XM_047442755.1:c.3528A>G, NM_182659.1:c.3237A>G, XR_007068451.1:n.4581A>G, XM_047442756.1:c.3372A>G, XR_007068452.1:n.4533A>G, NR_174404.1:n.2988A>G, NR_174405.1:n.3605A>G

                  9.

                  rs1474835561 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C [Show Flanks]
                    Chromosome:
                    Y:13369298 (GRCh38)
                    Y:15481178 (GRCh37)
                    Canonical SPDI:
                    NC_000024.10:13369297:T:C
                    Gene:
                    UTY (Varview)
                    Functional Consequence:
                    missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant
                    Validated:
                    by frequency
                    MAF:
                    C=0.00002/1 (GnomAD_exomes)
                    HGVS:
                    NC_000024.10:g.13369298T>C, NC_000024.9:g.15481178T>C, XM_011531455.4:c.697A>G, XM_011531455.3:c.697A>G, XM_011531455.2:c.697A>G, XM_011531455.1:c.697A>G, XM_011531453.4:c.697A>G, XM_011531453.3:c.697A>G, XM_011531453.2:c.697A>G, XM_011531453.1:c.697A>G, XM_011531454.4:c.697A>G, XM_011531454.3:c.697A>G, XM_011531454.2:c.697A>G, XM_011531454.1:c.697A>G, NM_007125.4:c.697A>G, XM_011531441.4:c.697A>G, XM_011531441.3:c.697A>G, XM_011531441.2:c.697A>G, XM_011531441.1:c.697A>G, XM_011531442.4:c.697A>G, XM_011531442.3:c.697A>G, XM_011531442.2:c.697A>G, XM_011531442.1:c.697A>G, XM_011531443.4:c.697A>G, XM_011531443.3:c.697A>G, XM_011531443.2:c.697A>G, XM_011531443.1:c.697A>G, XM_011531445.4:c.697A>G, XM_011531445.3:c.697A>G, XM_011531445.2:c.697A>G, XM_011531445.1:c.697A>G, XM_011531446.4:c.697A>G, XM_011531446.3:c.697A>G, XM_011531446.2:c.697A>G, XM_011531446.1:c.697A>G, XM_011531447.4:c.697A>G, XM_011531447.3:c.697A>G, XM_011531447.2:c.697A>G, XM_011531447.1:c.697A>G, XM_011531448.4:c.697A>G, XM_011531448.3:c.697A>G, XM_011531448.2:c.697A>G, XM_011531448.1:c.697A>G, XM_011531451.4:c.697A>G, XM_011531451.3:c.697A>G, XM_011531451.2:c.697A>G, XM_011531451.1:c.697A>G, XM_011531459.4:c.697A>G, XM_011531459.3:c.697A>G, XM_011531459.2:c.697A>G, XM_011531459.1:c.697A>G, XM_011531460.4:c.697A>G, XM_011531460.3:c.697A>G, XM_011531460.2:c.697A>G, XM_011531460.1:c.697A>G, XM_017030070.3:c.697A>G, XM_017030070.2:c.697A>G, XM_017030070.1:c.697A>G, XM_017030071.3:c.697A>G, XM_017030071.2:c.697A>G, XM_017030071.1:c.697A>G, XM_017030073.3:c.697A>G, XM_017030073.2:c.697A>G, XM_017030073.1:c.697A>G, NM_001258249.2:c.697A>G, NM_001258249.1:c.697A>G, XM_047442748.1:c.697A>G, XM_047442749.1:c.697A>G, XM_047442751.1:c.697A>G, XM_047442752.1:c.697A>G, XM_047442754.1:c.697A>G, NR_047607.1:n.1702A>G, NR_047598.1:n.1808A>G, NR_047624.1:n.1922A>G, XM_047442747.1:c.697A>G, NR_047645.1:n.1773A>G, XM_047442750.1:c.697A>G, NR_047644.1:n.1702A>G, NM_001258258.1:c.697A>G, NR_047599.1:n.1702A>G, NM_001258252.1:c.697A>G, NM_001258261.1:c.697A>G, NR_047603.1:n.1825A>G, NR_047597.1:n.1808A>G, NR_047642.1:n.1702A>G, NR_047618.1:n.1702A>G, NM_001258260.1:c.697A>G, NM_001258264.1:c.697A>G, NR_047637.1:n.1702A>G, NR_047641.1:n.1702A>G, NM_001258266.1:c.697A>G, XM_047442753.1:c.697A>G, NM_001258251.1:c.697A>G, NM_001258267.1:c.697A>G, NR_047602.1:n.1667A>G, NM_001258256.1:c.697A>G, NR_047647.1:n.1702A>G, NM_001258259.1:c.697A>G, NR_047600.1:n.1667A>G, NM_001258262.1:c.697A>G, NR_047638.1:n.1773A>G, NM_001258253.1:c.697A>G, NR_047646.1:n.1702A>G, NM_001258269.1:c.697A>G, NM_001258263.1:c.697A>G, NR_047635.1:n.1702A>G, NM_001258268.1:c.697A>G, NR_047632.1:n.1782A>G, NM_001258255.1:c.697A>G, NR_047609.1:n.1702A>G, NM_001258265.1:c.448A>G, XM_047442746.1:c.697A>G, NM_001258270.1:c.697A>G, NM_001258257.1:c.697A>G, NR_047643.1:n.1702A>G, NM_001258254.1:c.697A>G, NM_001400177.1:c.697A>G, NM_001258250.1:c.697A>G, NR_047612.1:n.1702A>G, NM_001400175.1:c.697A>G, NM_001400178.1:c.697A>G, NR_047614.1:n.1816A>G, NR_047629.1:n.1702A>G, NR_047621.1:n.1773A>G, NR_047623.1:n.1702A>G, NR_047601.1:n.1702A>G, NR_047622.1:n.1702A>G, NR_047617.1:n.1808A>G, NR_047608.1:n.1702A>G, NR_047615.1:n.1702A>G, NR_047636.1:n.1702A>G, NR_047606.1:n.1702A>G, NR_047611.1:n.1702A>G, NR_047631.1:n.1702A>G, NR_047610.1:n.1702A>G, NR_047628.1:n.1702A>G, NM_001400181.1:c.697A>G, NR_047605.1:n.1702A>G, NR_047613.1:n.1652A>G, NR_047616.1:n.1816A>G, NR_047633.1:n.1702A>G, NR_047627.1:n.1667A>G, NR_047626.1:n.1702A>G, NR_047596.1:n.1702A>G, NR_047634.1:n.1667A>G, NR_047640.1:n.1808A>G, NR_047620.1:n.1702A>G, NR_047630.1:n.1702A>G, NR_047625.1:n.1702A>G, NR_047619.1:n.1702A>G, NR_047604.1:n.1702A>G, NM_001400170.1:c.697A>G, NM_001400171.1:c.697A>G, NM_001400173.1:c.697A>G, XM_047442755.1:c.697A>G, NM_182659.1:c.697A>G, XR_007068451.1:n.1702A>G, XM_047442756.1:c.697A>G, XR_007068452.1:n.1702A>G, NR_174404.1:n.1065A>G, XM_047442757.1:c.697A>G, NR_174405.1:n.1065A>G, NM_182660.1:c.697A>G, NM_001400183.1:c.697A>G, NM_001400185.1:c.697A>G, NM_001400187.1:c.697A>G, NM_001400189.1:c.697A>G, NM_001400192.1:c.697A>G, NM_001400195.1:c.697A>G, NM_001400199.1:c.697A>G, XP_011529757.1:p.Asn233Asp, XP_011529755.1:p.Asn233Asp, XP_011529756.1:p.Asn233Asp, NP_009056.3:p.Asn233Asp, XP_011529743.1:p.Asn233Asp, XP_011529744.1:p.Asn233Asp, XP_011529745.1:p.Asn233Asp, XP_011529747.1:p.Asn233Asp, XP_011529748.1:p.Asn233Asp, XP_011529749.1:p.Asn233Asp, XP_011529750.1:p.Asn233Asp, XP_011529753.1:p.Asn233Asp, XP_011529761.1:p.Asn233Asp, XP_011529762.1:p.Asn233Asp, XP_016885559.1:p.Asn233Asp, XP_016885560.1:p.Asn233Asp, XP_016885562.1:p.Asn233Asp, NP_001245178.1:p.Asn233Asp, XP_047298704.1:p.Asn233Asp, XP_047298705.1:p.Asn233Asp, XP_047298707.1:p.Asn233Asp, XP_047298708.1:p.Asn233Asp, XP_047298710.1:p.Asn233Asp, XP_047298703.1:p.Asn233Asp, XP_047298706.1:p.Asn233Asp, NP_001245187.1:p.Asn233Asp, NP_001245181.1:p.Asn233Asp, NP_001245190.1:p.Asn233Asp, NP_001245189.1:p.Asn233Asp, NP_001245193.1:p.Asn233Asp, NP_001245195.1:p.Asn233Asp, XP_047298709.1:p.Asn233Asp, NP_001245180.1:p.Asn233Asp, NP_001245196.1:p.Asn233Asp, NP_001245185.1:p.Asn233Asp, NP_001245188.1:p.Asn233Asp, NP_001245191.1:p.Asn233Asp, NP_001245182.1:p.Asn233Asp, NP_001245198.1:p.Asn233Asp, NP_001245192.1:p.Asn233Asp, NP_001245197.1:p.Asn233Asp, NP_001245184.1:p.Asn233Asp, NP_001245194.1:p.Asn150Asp, XP_047298702.1:p.Asn233Asp, NP_001245199.1:p.Asn233Asp, NP_001245186.1:p.Asn233Asp, NP_001245183.1:p.Asn233Asp, NP_001387106.1:p.Asn233Asp, NP_001245179.1:p.Asn233Asp, NP_001387104.1:p.Asn233Asp, NP_001387107.1:p.Asn233Asp, NP_001387110.1:p.Asn233Asp, NP_001387099.1:p.Asn233Asp, NP_001387100.1:p.Asn233Asp, NP_001387102.1:p.Asn233Asp, XP_047298711.1:p.Asn233Asp, NP_872600.1:p.Asn233Asp, XP_047298712.1:p.Asn233Asp, XP_047298713.1:p.Asn233Asp, NP_872601.1:p.Asn233Asp, NP_001387112.1:p.Asn233Asp, NP_001387114.1:p.Asn233Asp, NP_001387116.1:p.Asn233Asp, NP_001387118.1:p.Asn233Asp, NP_001387121.1:p.Asn233Asp, NP_001387124.1:p.Asn233Asp, NP_001387128.1:p.Asn233Asp

                    10.

                    rs1473383015 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>G [Show Flanks]
                      Chromosome:
                      Y:13355386 (GRCh38)
                      Y:15467266 (GRCh37)
                      Canonical SPDI:
                      NC_000024.10:13355385:C:G
                      Gene:
                      UTY (Varview)
                      Functional Consequence:
                      missense_variant,coding_sequence_variant,non_coding_transcript_variant
                      Validated:
                      by frequency
                      MAF:
                      G=0.00001/1 (GnomAD_exomes)
                      HGVS:
                      NC_000024.10:g.13355386C>G, NC_000024.9:g.15467266C>G, XM_011531455.4:c.1678G>C, XM_011531455.3:c.1678G>C, XM_011531455.2:c.1678G>C, XM_011531455.1:c.1678G>C, XM_011531453.4:c.1678G>C, XM_011531453.3:c.1678G>C, XM_011531453.2:c.1678G>C, XM_011531453.1:c.1678G>C, XM_011531454.4:c.1678G>C, XM_011531454.3:c.1678G>C, XM_011531454.2:c.1678G>C, XM_011531454.1:c.1678G>C, NM_007125.4:c.1387G>C, XM_011531441.4:c.1678G>C, XM_011531441.3:c.1678G>C, XM_011531441.2:c.1678G>C, XM_011531441.1:c.1678G>C, XM_011531442.4:c.1678G>C, XM_011531442.3:c.1678G>C, XM_011531442.2:c.1678G>C, XM_011531442.1:c.1678G>C, XM_011531443.4:c.1612G>C, XM_011531443.3:c.1612G>C, XM_011531443.2:c.1612G>C, XM_011531443.1:c.1612G>C, XM_011531445.4:c.1543G>C, XM_011531445.3:c.1543G>C, XM_011531445.2:c.1543G>C, XM_011531445.1:c.1543G>C, XM_011531446.4:c.1522G>C, XM_011531446.3:c.1522G>C, XM_011531446.2:c.1522G>C, XM_011531446.1:c.1522G>C, XM_011531447.4:c.1543G>C, XM_011531447.3:c.1543G>C, XM_011531447.2:c.1543G>C, XM_011531447.1:c.1543G>C, XM_011531448.4:c.1477G>C, XM_011531448.3:c.1477G>C, XM_011531448.2:c.1477G>C, XM_011531448.1:c.1477G>C, XM_011531451.4:c.1387G>C, XM_011531451.3:c.1387G>C, XM_011531451.2:c.1387G>C, XM_011531451.1:c.1387G>C, XM_011531459.4:c.1678G>C, XM_011531459.3:c.1678G>C, XM_011531459.2:c.1678G>C, XM_011531459.1:c.1678G>C, XM_011531460.4:c.1678G>C, XM_011531460.3:c.1678G>C, XM_011531460.2:c.1678G>C, XM_011531460.1:c.1678G>C, XM_017030070.3:c.1678G>C, XM_017030070.2:c.1678G>C, XM_017030070.1:c.1678G>C, XM_017030071.3:c.1678G>C, XM_017030071.2:c.1678G>C, XM_017030071.1:c.1678G>C, XM_017030073.3:c.1387G>C, XM_017030073.2:c.1387G>C, XM_017030073.1:c.1387G>C, NM_001258249.2:c.1678G>C, NM_001258249.1:c.1678G>C, XM_047442748.1:c.1678G>C, XM_047442749.1:c.1612G>C, XM_047442751.1:c.1522G>C, XM_047442752.1:c.1543G>C, XM_047442754.1:c.1522G>C, NR_047607.1:n.2738G>C, NR_047598.1:n.2628G>C, NR_047624.1:n.2612G>C, XM_047442747.1:c.1678G>C, NR_047645.1:n.2598G>C, XM_047442750.1:c.1543G>C, NR_047644.1:n.2585G>C, NM_001258258.1:c.1543G>C, NR_047599.1:n.2392G>C, NM_001258252.1:c.1522G>C, NM_001258261.1:c.1513G>C, NR_047603.1:n.2515G>C, NR_047597.1:n.2498G>C, NR_047642.1:n.2392G>C, NR_047618.1:n.2683G>C, NM_001258260.1:c.1477G>C, NM_001258264.1:c.1474G>C, NR_047637.1:n.2450G>C, NR_047641.1:n.2392G>C, NM_001258266.1:c.1522G>C, XM_047442753.1:c.1522G>C, NM_001258251.1:c.1387G>C, NM_001258267.1:c.1387G>C, NR_047602.1:n.2357G>C, NM_001258256.1:c.1522G>C, NR_047647.1:n.2349G>C, NM_001258259.1:c.1339G>C, NR_047600.1:n.2688G>C, NM_001258262.1:c.1678G>C, NR_047638.1:n.2458G>C, NM_001258253.1:c.1387G>C, NR_047646.1:n.2265G>C, NM_001258269.1:c.1612G>C, NM_001258263.1:c.1387G>C, NR_047635.1:n.2387G>C, NM_001258268.1:c.1522G>C, NR_047632.1:n.2472G>C, NM_001258255.1:c.1522G>C, NR_047609.1:n.2522G>C, NM_001258265.1:c.1138G>C, XM_047442746.1:c.1612G>C, NM_001258270.1:c.1387G>C, NM_001258257.1:c.1387G>C, NR_047643.1:n.2527G>C, NM_001258254.1:c.1522G>C, NM_001400177.1:c.1612G>C, NM_001258250.1:c.1339G>C, NR_047612.1:n.2683G>C, NM_001400175.1:c.1612G>C, NM_001400178.1:c.1522G>C, NR_047614.1:n.2596G>C, NR_047629.1:n.2392G>C, NR_047621.1:n.2754G>C, NR_047623.1:n.2527G>C, NR_047601.1:n.2527G>C, NR_047622.1:n.2584G>C, NR_047617.1:n.2654G>C, NR_047608.1:n.2479G>C, NR_047615.1:n.2450G>C, NR_047636.1:n.2482G>C, NR_047606.1:n.2528G>C, NR_047611.1:n.2527G>C, NR_047631.1:n.2392G>C, NR_047610.1:n.2392G>C, NR_047628.1:n.2392G>C, NM_001400181.1:c.1387G>C, NR_047605.1:n.2344G>C, NR_047613.1:n.2633G>C, NR_047616.1:n.2506G>C, NR_047633.1:n.2813G>C, NR_047627.1:n.2357G>C, NR_047626.1:n.2392G>C, NR_047596.1:n.2392G>C, NR_047634.1:n.2513G>C, NR_047640.1:n.2498G>C, NR_047620.1:n.2527G>C, NR_047630.1:n.2392G>C, NR_047639.1:n.2298G>C, NR_047625.1:n.2265G>C, NR_047619.1:n.2450G>C, NR_047604.1:n.2392G>C, NM_001400170.1:c.1522G>C, NM_001400171.1:c.1477G>C, NM_001400173.1:c.1387G>C, XM_047442755.1:c.1678G>C, NM_182659.1:c.1387G>C, XR_007068451.1:n.2683G>C, XM_047442756.1:c.1522G>C, XR_007068452.1:n.2683G>C, NR_174404.1:n.1911G>C, XM_047442757.1:c.1612G>C, NR_174405.1:n.1755G>C, NM_182660.1:c.1387G>C, NM_001400183.1:c.1678G>C, NM_001400185.1:c.1612G>C, NM_001400187.1:c.1522G>C, NM_001400189.1:c.1477G>C, NM_001400192.1:c.1522G>C, NM_001400195.1:c.1477G>C, NM_001400199.1:c.1387G>C, XP_011529757.1:p.Glu560Gln, XP_011529755.1:p.Glu560Gln, XP_011529756.1:p.Glu560Gln, NP_009056.3:p.Glu463Gln, XP_011529743.1:p.Glu560Gln, XP_011529744.1:p.Glu560Gln, XP_011529745.1:p.Glu538Gln, XP_011529747.1:p.Glu515Gln, XP_011529748.1:p.Glu508Gln, XP_011529749.1:p.Glu515Gln, XP_011529750.1:p.Glu493Gln, XP_011529753.1:p.Glu463Gln, XP_011529761.1:p.Glu560Gln, XP_011529762.1:p.Glu560Gln, XP_016885559.1:p.Glu560Gln, XP_016885560.1:p.Glu560Gln, XP_016885562.1:p.Glu463Gln, NP_001245178.1:p.Glu560Gln, XP_047298704.1:p.Glu560Gln, XP_047298705.1:p.Glu538Gln, XP_047298707.1:p.Glu508Gln, XP_047298708.1:p.Glu515Gln, XP_047298710.1:p.Glu508Gln, XP_047298703.1:p.Glu560Gln, XP_047298706.1:p.Glu515Gln, NP_001245187.1:p.Glu515Gln, NP_001245181.1:p.Glu508Gln, NP_001245190.1:p.Glu505Gln, NP_001245189.1:p.Glu493Gln, NP_001245193.1:p.Glu492Gln, NP_001245195.1:p.Glu508Gln, XP_047298709.1:p.Glu508Gln, NP_001245180.1:p.Glu463Gln, NP_001245196.1:p.Glu463Gln, NP_001245185.1:p.Glu508Gln, NP_001245188.1:p.Glu447Gln, NP_001245191.1:p.Glu560Gln, NP_001245182.1:p.Glu463Gln, NP_001245198.1:p.Glu538Gln, NP_001245192.1:p.Glu463Gln, NP_001245197.1:p.Glu508Gln, NP_001245184.1:p.Glu508Gln, NP_001245194.1:p.Glu380Gln, XP_047298702.1:p.Glu538Gln, NP_001245199.1:p.Glu463Gln, NP_001245186.1:p.Glu463Gln, NP_001245183.1:p.Glu508Gln, NP_001387106.1:p.Glu538Gln, NP_001245179.1:p.Glu447Gln, NP_001387104.1:p.Glu538Gln, NP_001387107.1:p.Glu508Gln, NP_001387110.1:p.Glu463Gln, NP_001387099.1:p.Glu508Gln, NP_001387100.1:p.Glu493Gln, NP_001387102.1:p.Glu463Gln, XP_047298711.1:p.Glu560Gln, NP_872600.1:p.Glu463Gln, XP_047298712.1:p.Glu508Gln, XP_047298713.1:p.Glu538Gln, NP_872601.1:p.Glu463Gln, NP_001387112.1:p.Glu560Gln, NP_001387114.1:p.Glu538Gln, NP_001387116.1:p.Glu508Gln, NP_001387118.1:p.Glu493Gln, NP_001387121.1:p.Glu508Gln, NP_001387124.1:p.Glu493Gln, NP_001387128.1:p.Glu463Gln

                      11.

                      rs1472399494 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        Y:13336106 (GRCh38)
                        Y:15447986 (GRCh37)
                        Canonical SPDI:
                        NC_000024.10:13336105:C:T
                        Gene:
                        UTY (Varview)
                        Functional Consequence:
                        missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant
                        Validated:
                        by frequency
                        MAF:
                        T=0.00001/1 (GnomAD_exomes)
                        HGVS:
                        NC_000024.10:g.13336106C>T, NC_000024.9:g.15447986C>T, XM_011531455.4:c.2339G>A, XM_011531455.3:c.2339G>A, XM_011531455.2:c.2339G>A, XM_011531455.1:c.2339G>A, XM_011531453.4:c.2339G>A, XM_011531453.3:c.2339G>A, XM_011531453.2:c.2339G>A, XM_011531453.1:c.2339G>A, XM_011531454.4:c.2339G>A, XM_011531454.3:c.2339G>A, XM_011531454.2:c.2339G>A, XM_011531454.1:c.2339G>A, NM_007125.4:c.2000G>A, XM_011531441.4:c.2339G>A, XM_011531441.3:c.2339G>A, XM_011531441.2:c.2339G>A, XM_011531441.1:c.2339G>A, XM_011531442.4:c.2291G>A, XM_011531442.3:c.2291G>A, XM_011531442.2:c.2291G>A, XM_011531442.1:c.2291G>A, XM_011531443.4:c.2273G>A, XM_011531443.3:c.2273G>A, XM_011531443.2:c.2273G>A, XM_011531443.1:c.2273G>A, XM_011531445.4:c.2204G>A, XM_011531445.3:c.2204G>A, XM_011531445.2:c.2204G>A, XM_011531445.1:c.2204G>A, XM_011531446.4:c.2183G>A, XM_011531446.3:c.2183G>A, XM_011531446.2:c.2183G>A, XM_011531446.1:c.2183G>A, XM_011531447.4:c.2156G>A, XM_011531447.3:c.2156G>A, XM_011531447.2:c.2156G>A, XM_011531447.1:c.2156G>A, XM_011531448.4:c.2138G>A, XM_011531448.3:c.2138G>A, XM_011531448.2:c.2138G>A, XM_011531448.1:c.2138G>A, XM_011531451.4:c.2048G>A, XM_011531451.3:c.2048G>A, XM_011531451.2:c.2048G>A, XM_011531451.1:c.2048G>A, XM_011531459.4:c.2339G>A, XM_011531459.3:c.2339G>A, XM_011531459.2:c.2339G>A, XM_011531459.1:c.2339G>A, XM_011531460.4:c.2339G>A, XM_011531460.3:c.2339G>A, XM_011531460.2:c.2339G>A, XM_011531460.1:c.2339G>A, XM_017030070.3:c.2339G>A, XM_017030070.2:c.2339G>A, XM_017030070.1:c.2339G>A, XM_017030071.3:c.2339G>A, XM_017030071.2:c.2339G>A, XM_017030071.1:c.2339G>A, XM_017030073.3:c.2048G>A, XM_017030073.2:c.2048G>A, XM_017030073.1:c.2048G>A, NM_001258249.2:c.2291G>A, NM_001258249.1:c.2291G>A, XM_047442748.1:c.2291G>A, XM_047442749.1:c.2225G>A, XM_047442751.1:c.2183G>A, XM_047442752.1:c.2156G>A, XM_047442754.1:c.2135G>A, NR_047607.1:n.3351G>A, NR_047598.1:n.3241G>A, NR_047624.1:n.3225G>A, XM_047442747.1:c.2291G>A, NR_047645.1:n.3211G>A, XM_047442750.1:c.2204G>A, NR_047644.1:n.3198G>A, NM_001258258.1:c.2156G>A, NR_047599.1:n.3005G>A, NM_001258252.1:c.2135G>A, NM_001258261.1:c.2126G>A, NR_047603.1:n.3128G>A, NR_047597.1:n.3111G>A, NR_047642.1:n.3005G>A, NR_047618.1:n.3014G>A, NM_001258260.1:c.2090G>A, NM_001258264.1:c.2087G>A, NR_047637.1:n.3063G>A, NR_047641.1:n.3005G>A, NM_001258266.1:c.2135G>A, XM_047442753.1:c.2135G>A, NM_001258251.1:c.2048G>A, NM_001258267.1:c.2000G>A, NR_047602.1:n.2970G>A, NM_001258256.1:c.2135G>A, NR_047647.1:n.2962G>A, NM_001258259.1:c.1952G>A, NR_047600.1:n.2929G>A, NM_001258262.1:c.1919G>A, NR_047638.1:n.3071G>A, NM_001258253.1:c.2048G>A, NR_047646.1:n.2878G>A, NM_001258269.1:c.1853G>A, NM_001258263.1:c.2000G>A, NR_047635.1:n.3000G>A, NM_001258268.1:c.1763G>A, NR_047632.1:n.2713G>A, NM_001258255.1:c.1763G>A, NR_047609.1:n.2763G>A, NM_001258265.1:c.1751G>A, XM_047442746.1:c.2225G>A, NM_001258270.1:c.1628G>A, NM_001258257.1:c.1628G>A, NM_001258254.1:c.1763G>A, NM_001400177.1:c.2225G>A, NM_001258250.1:c.1580G>A, NM_001400175.1:c.2225G>A, NM_001400178.1:c.2135G>A, NM_001400181.1:c.2000G>A, NM_001400170.1:c.2135G>A, NM_001400171.1:c.2090G>A, NM_001400173.1:c.2000G>A, XM_047442755.1:c.2291G>A, NM_182659.1:c.2000G>A, XR_007068451.1:n.3344G>A, XM_047442756.1:c.2135G>A, XR_007068452.1:n.3296G>A, XM_047442757.1:c.2273G>A, NR_174405.1:n.2368G>A, NM_182660.1:c.2000G>A, NM_001400183.1:c.2291G>A, NM_001400185.1:c.2225G>A, NM_001400187.1:c.2183G>A, NM_001400189.1:c.2138G>A, NM_001400192.1:c.2135G>A, NM_001400195.1:c.2090G>A, NM_001400199.1:c.2048G>A, XP_011529757.1:p.Ser780Asn, XP_011529755.1:p.Ser780Asn, XP_011529756.1:p.Ser780Asn, NP_009056.3:p.Ser667Asn, XP_011529743.1:p.Ser780Asn, XP_011529744.1:p.Ser764Asn, XP_011529745.1:p.Ser758Asn, XP_011529747.1:p.Ser735Asn, XP_011529748.1:p.Ser728Asn, XP_011529749.1:p.Ser719Asn, XP_011529750.1:p.Ser713Asn, XP_011529753.1:p.Ser683Asn, XP_011529761.1:p.Ser780Asn, XP_011529762.1:p.Ser780Asn, XP_016885559.1:p.Ser780Asn, XP_016885560.1:p.Ser780Asn, XP_016885562.1:p.Ser683Asn, NP_001245178.1:p.Ser764Asn, XP_047298704.1:p.Ser764Asn, XP_047298705.1:p.Ser742Asn, XP_047298707.1:p.Ser728Asn, XP_047298708.1:p.Ser719Asn, XP_047298710.1:p.Ser712Asn, XP_047298703.1:p.Ser764Asn, XP_047298706.1:p.Ser735Asn, NP_001245187.1:p.Ser719Asn, NP_001245181.1:p.Ser712Asn, NP_001245190.1:p.Ser709Asn, NP_001245189.1:p.Ser697Asn, NP_001245193.1:p.Ser696Asn, NP_001245195.1:p.Ser712Asn, XP_047298709.1:p.Ser712Asn, NP_001245180.1:p.Ser683Asn, NP_001245196.1:p.Ser667Asn, NP_001245185.1:p.Ser712Asn, NP_001245188.1:p.Ser651Asn, NP_001245191.1:p.Ser640Asn, NP_001245182.1:p.Ser683Asn, NP_001245198.1:p.Ser618Asn, NP_001245192.1:p.Ser667Asn, NP_001245197.1:p.Ser588Asn, NP_001245184.1:p.Ser588Asn, NP_001245194.1:p.Ser584Asn, XP_047298702.1:p.Ser742Asn, NP_001245199.1:p.Ser543Asn, NP_001245186.1:p.Ser543Asn, NP_001245183.1:p.Ser588Asn, NP_001387106.1:p.Ser742Asn, NP_001245179.1:p.Ser527Asn, NP_001387104.1:p.Ser742Asn, NP_001387107.1:p.Ser712Asn, NP_001387110.1:p.Ser667Asn, NP_001387099.1:p.Ser712Asn, NP_001387100.1:p.Ser697Asn, NP_001387102.1:p.Ser667Asn, XP_047298711.1:p.Ser764Asn, NP_872600.1:p.Ser667Asn, XP_047298712.1:p.Ser712Asn, XP_047298713.1:p.Ser758Asn, NP_872601.1:p.Ser667Asn, NP_001387112.1:p.Ser764Asn, NP_001387114.1:p.Ser742Asn, NP_001387116.1:p.Ser728Asn, NP_001387118.1:p.Ser713Asn, NP_001387121.1:p.Ser712Asn, NP_001387124.1:p.Ser697Asn, NP_001387128.1:p.Ser683Asn

                        12.

                        rs1469956766 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>G [Show Flanks]
                          Chromosome:
                          Y:13369310 (GRCh38)
                          Y:15481190 (GRCh37)
                          Canonical SPDI:
                          NC_000024.10:13369309:A:G
                          Gene:
                          UTY (Varview)
                          Functional Consequence:
                          intron_variant,coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
                          Validated:
                          by frequency
                          MAF:
                          G=0.00002/1 (GnomAD_exomes)
                          HGVS:
                          NC_000024.10:g.13369310A>G, NC_000024.9:g.15481190A>G, XM_011531455.4:c.685T>C, XM_011531455.3:c.685T>C, XM_011531455.2:c.685T>C, XM_011531455.1:c.685T>C, XM_011531453.4:c.685T>C, XM_011531453.3:c.685T>C, XM_011531453.2:c.685T>C, XM_011531453.1:c.685T>C, XM_011531454.4:c.685T>C, XM_011531454.3:c.685T>C, XM_011531454.2:c.685T>C, XM_011531454.1:c.685T>C, NM_007125.4:c.685T>C, XM_011531441.4:c.685T>C, XM_011531441.3:c.685T>C, XM_011531441.2:c.685T>C, XM_011531441.1:c.685T>C, XM_011531442.4:c.685T>C, XM_011531442.3:c.685T>C, XM_011531442.2:c.685T>C, XM_011531442.1:c.685T>C, XM_011531443.4:c.685T>C, XM_011531443.3:c.685T>C, XM_011531443.2:c.685T>C, XM_011531443.1:c.685T>C, XM_011531445.4:c.685T>C, XM_011531445.3:c.685T>C, XM_011531445.2:c.685T>C, XM_011531445.1:c.685T>C, XM_011531446.4:c.685T>C, XM_011531446.3:c.685T>C, XM_011531446.2:c.685T>C, XM_011531446.1:c.685T>C, XM_011531447.4:c.685T>C, XM_011531447.3:c.685T>C, XM_011531447.2:c.685T>C, XM_011531447.1:c.685T>C, XM_011531448.4:c.685T>C, XM_011531448.3:c.685T>C, XM_011531448.2:c.685T>C, XM_011531448.1:c.685T>C, XM_011531451.4:c.685T>C, XM_011531451.3:c.685T>C, XM_011531451.2:c.685T>C, XM_011531451.1:c.685T>C, XM_011531459.4:c.685T>C, XM_011531459.3:c.685T>C, XM_011531459.2:c.685T>C, XM_011531459.1:c.685T>C, XM_011531460.4:c.685T>C, XM_011531460.3:c.685T>C, XM_011531460.2:c.685T>C, XM_011531460.1:c.685T>C, XM_017030070.3:c.685T>C, XM_017030070.2:c.685T>C, XM_017030070.1:c.685T>C, XM_017030071.3:c.685T>C, XM_017030071.2:c.685T>C, XM_017030071.1:c.685T>C, XM_017030073.3:c.685T>C, XM_017030073.2:c.685T>C, XM_017030073.1:c.685T>C, NM_001258249.2:c.685T>C, NM_001258249.1:c.685T>C, XM_047442748.1:c.685T>C, XM_047442749.1:c.685T>C, XM_047442751.1:c.685T>C, XM_047442752.1:c.685T>C, XM_047442754.1:c.685T>C, NR_047607.1:n.1690T>C, NR_047598.1:n.1796T>C, NR_047624.1:n.1910T>C, XM_047442747.1:c.685T>C, NR_047645.1:n.1761T>C, XM_047442750.1:c.685T>C, NR_047644.1:n.1690T>C, NM_001258258.1:c.685T>C, NR_047599.1:n.1690T>C, NM_001258252.1:c.685T>C, NM_001258261.1:c.685T>C, NR_047603.1:n.1813T>C, NR_047597.1:n.1796T>C, NR_047642.1:n.1690T>C, NR_047618.1:n.1690T>C, NM_001258260.1:c.685T>C, NM_001258264.1:c.685T>C, NR_047637.1:n.1690T>C, NR_047641.1:n.1690T>C, NM_001258266.1:c.685T>C, XM_047442753.1:c.685T>C, NM_001258251.1:c.685T>C, NM_001258267.1:c.685T>C, NR_047602.1:n.1655T>C, NM_001258256.1:c.685T>C, NR_047647.1:n.1690T>C, NM_001258259.1:c.685T>C, NR_047600.1:n.1655T>C, NM_001258262.1:c.685T>C, NR_047638.1:n.1761T>C, NM_001258253.1:c.685T>C, NR_047646.1:n.1690T>C, NM_001258269.1:c.685T>C, NM_001258263.1:c.685T>C, NR_047635.1:n.1690T>C, NM_001258268.1:c.685T>C, NR_047632.1:n.1770T>C, NM_001258255.1:c.685T>C, NR_047609.1:n.1690T>C, NM_001258265.1:c.436T>C, XM_047442746.1:c.685T>C, NM_001258270.1:c.685T>C, NM_001258257.1:c.685T>C, NR_047643.1:n.1690T>C, NM_001258254.1:c.685T>C, NM_001400177.1:c.685T>C, NM_001258250.1:c.685T>C, NR_047612.1:n.1690T>C, NM_001400175.1:c.685T>C, NM_001400178.1:c.685T>C, NR_047614.1:n.1804T>C, NR_047629.1:n.1690T>C, NR_047621.1:n.1761T>C, NR_047623.1:n.1690T>C, NR_047601.1:n.1690T>C, NR_047622.1:n.1690T>C, NR_047617.1:n.1796T>C, NR_047608.1:n.1690T>C, NR_047615.1:n.1690T>C, NR_047636.1:n.1690T>C, NR_047606.1:n.1690T>C, NR_047611.1:n.1690T>C, NR_047631.1:n.1690T>C, NR_047610.1:n.1690T>C, NR_047628.1:n.1690T>C, NM_001400181.1:c.685T>C, NR_047605.1:n.1690T>C, NR_047613.1:n.1640T>C, NR_047616.1:n.1804T>C, NR_047633.1:n.1690T>C, NR_047627.1:n.1655T>C, NR_047626.1:n.1690T>C, NR_047596.1:n.1690T>C, NR_047634.1:n.1655T>C, NR_047640.1:n.1796T>C, NR_047620.1:n.1690T>C, NR_047630.1:n.1690T>C, NR_047625.1:n.1690T>C, NR_047619.1:n.1690T>C, NR_047604.1:n.1690T>C, NM_001400170.1:c.685T>C, NM_001400171.1:c.685T>C, NM_001400173.1:c.685T>C, XM_047442755.1:c.685T>C, NM_182659.1:c.685T>C, XR_007068451.1:n.1690T>C, XM_047442756.1:c.685T>C, XR_007068452.1:n.1690T>C, NR_174404.1:n.1053T>C, XM_047442757.1:c.685T>C, NR_174405.1:n.1053T>C, NM_182660.1:c.685T>C, NM_001400183.1:c.685T>C, NM_001400185.1:c.685T>C, NM_001400187.1:c.685T>C, NM_001400189.1:c.685T>C, NM_001400192.1:c.685T>C, NM_001400195.1:c.685T>C, NM_001400199.1:c.685T>C

                          13.

                          rs1469531525 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>T [Show Flanks]
                            Chromosome:
                            Y:13297718 (GRCh38)
                            Y:15409598 (GRCh37)
                            Canonical SPDI:
                            NC_000024.10:13297717:A:T
                            Gene:
                            UTY (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,coding_sequence_variant,genic_downstream_transcript_variant,missense_variant,non_coding_transcript_variant
                            Validated:
                            by frequency
                            MAF:
                            T=0.00001/1 (GnomAD_exomes)
                            HGVS:
                            NC_000024.10:g.13297718A>T, NC_000024.9:g.15409598A>T, XM_011531455.4:c.4047T>A, XM_011531455.3:c.4047T>A, XM_011531455.2:c.4047T>A, XM_011531455.1:c.4047T>A, XM_011531453.4:c.4047T>A, XM_011531453.3:c.4047T>A, XM_011531453.2:c.4047T>A, XM_011531453.1:c.4047T>A, XM_011531454.4:c.4047T>A, XM_011531454.3:c.4047T>A, XM_011531454.2:c.4047T>A, XM_011531454.1:c.4047T>A, NM_007125.4:c.3708T>A, XM_011531441.4:c.4047T>A, XM_011531441.3:c.4047T>A, XM_011531441.2:c.4047T>A, XM_011531441.1:c.4047T>A, XM_011531442.4:c.3999T>A, XM_011531442.3:c.3999T>A, XM_011531442.2:c.3999T>A, XM_011531442.1:c.3999T>A, XM_011531443.4:c.3981T>A, XM_011531443.3:c.3981T>A, XM_011531443.2:c.3981T>A, XM_011531443.1:c.3981T>A, XM_011531445.4:c.3912T>A, XM_011531445.3:c.3912T>A, XM_011531445.2:c.3912T>A, XM_011531445.1:c.3912T>A, XM_011531446.4:c.3891T>A, XM_011531446.3:c.3891T>A, XM_011531446.2:c.3891T>A, XM_011531446.1:c.3891T>A, XM_011531447.4:c.3864T>A, XM_011531447.3:c.3864T>A, XM_011531447.2:c.3864T>A, XM_011531447.1:c.3864T>A, XM_011531448.4:c.3846T>A, XM_011531448.3:c.3846T>A, XM_011531448.2:c.3846T>A, XM_011531448.1:c.3846T>A, XM_011531451.4:c.3756T>A, XM_011531451.3:c.3756T>A, XM_011531451.2:c.3756T>A, XM_011531451.1:c.3756T>A, XM_011531459.4:c.4047T>A, XM_011531459.3:c.4047T>A, XM_011531459.2:c.4047T>A, XM_011531459.1:c.4047T>A, XM_017030070.3:c.*118T>A, NM_001258249.2:c.3999T>A, NM_001258249.1:c.3999T>A, XM_047442748.1:c.3999T>A, XM_047442749.1:c.3933T>A, XM_047442751.1:c.3891T>A, XM_047442752.1:c.3864T>A, XM_047442754.1:c.3843T>A, NR_047607.1:n.5059T>A, NR_047598.1:n.5017T>A, NR_047624.1:n.4933T>A, XM_047442747.1:c.3999T>A, NR_047645.1:n.4919T>A, XM_047442750.1:c.3912T>A, NR_047644.1:n.4906T>A, NM_001258258.1:c.3864T>A, NR_047599.1:n.4836T>A, NM_001258252.1:c.3843T>A, NM_001258261.1:c.3834T>A, NR_047603.1:n.4836T>A, NR_047597.1:n.4819T>A, NR_047642.1:n.4713T>A, NR_047618.1:n.4814T>A, NM_001258260.1:c.3798T>A, NM_001258264.1:c.3795T>A, NR_047637.1:n.4771T>A, NR_047641.1:n.4781T>A, NM_001258266.1:c.3768T>A, XM_047442753.1:c.3843T>A, NM_001258251.1:c.3756T>A, NM_001258267.1:c.3708T>A, NR_047602.1:n.4678T>A, NM_001258256.1:c.3843T>A, NR_047647.1:n.4670T>A, NM_001258259.1:c.3660T>A, NR_047600.1:n.4637T>A, NM_001258262.1:c.3627T>A, NR_047638.1:n.4779T>A, NM_001258253.1:c.3756T>A, NR_047646.1:n.4586T>A, NM_001258269.1:c.3561T>A, NM_001258263.1:c.3708T>A, NR_047635.1:n.4708T>A, NM_001258268.1:c.3471T>A, NR_047632.1:n.4489T>A, NM_001258255.1:c.3471T>A, NR_047609.1:n.4471T>A, NM_001258265.1:c.3459T>A, XM_047442746.1:c.3933T>A, NM_001258270.1:c.3336T>A, NM_001258257.1:c.3336T>A, NR_047643.1:n.4313T>A, NM_001258254.1:c.3471T>A, NM_001400177.1:c.3933T>A, NM_001258250.1:c.3288T>A, NR_047612.1:n.4231T>A, NM_001400175.1:c.3933T>A, NM_001400178.1:c.3843T>A, NR_047614.1:n.4212T>A, NR_047629.1:n.4207T>A, NR_047621.1:n.4180T>A, NR_047623.1:n.4143T>A, NR_047601.1:n.4313T>A, NR_047622.1:n.4132T>A, NR_047617.1:n.4109T>A, NR_047608.1:n.4095T>A, NR_047615.1:n.4066T>A, NR_047636.1:n.4078T>A, NR_047606.1:n.4076T>A, NR_047611.1:n.4075T>A, NR_047631.1:n.4032T>A, NR_047610.1:n.4008T>A, NR_047628.1:n.3988T>A, NM_001400181.1:c.3708T>A, NR_047605.1:n.3892T>A, NR_047613.1:n.3993T>A, NR_047616.1:n.3992T>A, NR_047633.1:n.3989T>A, NR_047627.1:n.3955T>A, NR_047626.1:n.3940T>A, NR_047596.1:n.3940T>A, NR_047634.1:n.3939T>A, NR_047640.1:n.3924T>A, NR_047620.1:n.4075T>A, NR_047630.1:n.3865T>A, NR_047639.1:n.3846T>A, NR_047625.1:n.3813T>A, NR_047619.1:n.3998T>A, NR_047604.1:n.3806T>A, NM_001400170.1:c.3843T>A, NM_001400171.1:c.3798T>A, NM_001400173.1:c.3708T>A, XM_047442755.1:c.3999T>A, NM_182659.1:c.3708T>A, XM_047442756.1:c.*118T>A, NR_174404.1:n.3459T>A, NR_174405.1:n.4168T>A, XP_011529757.1:p.Phe1349Leu, XP_011529755.1:p.Phe1349Leu, XP_011529756.1:p.Phe1349Leu, NP_009056.3:p.Phe1236Leu, XP_011529743.1:p.Phe1349Leu, XP_011529744.1:p.Phe1333Leu, XP_011529745.1:p.Phe1327Leu, XP_011529747.1:p.Phe1304Leu, XP_011529748.1:p.Phe1297Leu, XP_011529749.1:p.Phe1288Leu, XP_011529750.1:p.Phe1282Leu, XP_011529753.1:p.Phe1252Leu, XP_011529761.1:p.Phe1349Leu, NP_001245178.1:p.Phe1333Leu, XP_047298704.1:p.Phe1333Leu, XP_047298705.1:p.Phe1311Leu, XP_047298707.1:p.Phe1297Leu, XP_047298708.1:p.Phe1288Leu, XP_047298710.1:p.Phe1281Leu, XP_047298703.1:p.Phe1333Leu, XP_047298706.1:p.Phe1304Leu, NP_001245187.1:p.Phe1288Leu, NP_001245181.1:p.Phe1281Leu, NP_001245190.1:p.Phe1278Leu, NP_001245189.1:p.Phe1266Leu, NP_001245193.1:p.Phe1265Leu, NP_001245195.1:p.Phe1256Leu, XP_047298709.1:p.Phe1281Leu, NP_001245180.1:p.Phe1252Leu, NP_001245196.1:p.Phe1236Leu, NP_001245185.1:p.Phe1281Leu, NP_001245188.1:p.Phe1220Leu, NP_001245191.1:p.Phe1209Leu, NP_001245182.1:p.Phe1252Leu, NP_001245198.1:p.Phe1187Leu, NP_001245192.1:p.Phe1236Leu, NP_001245197.1:p.Phe1157Leu, NP_001245184.1:p.Phe1157Leu, NP_001245194.1:p.Phe1153Leu, XP_047298702.1:p.Phe1311Leu, NP_001245199.1:p.Phe1112Leu, NP_001245186.1:p.Phe1112Leu, NP_001245183.1:p.Phe1157Leu, NP_001387106.1:p.Phe1311Leu, NP_001245179.1:p.Phe1096Leu, NP_001387104.1:p.Phe1311Leu, NP_001387107.1:p.Phe1281Leu, NP_001387110.1:p.Phe1236Leu, NP_001387099.1:p.Phe1281Leu, NP_001387100.1:p.Phe1266Leu, NP_001387102.1:p.Phe1236Leu, XP_047298711.1:p.Phe1333Leu, NP_872600.1:p.Phe1236Leu

                            14.

                            rs1464752363 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>T [Show Flanks]
                              Chromosome:
                              Y:13335622 (GRCh38)
                              Y:15447502 (GRCh37)
                              Canonical SPDI:
                              NC_000024.10:13335621:G:T
                              Gene:
                              UTY (Varview)
                              Functional Consequence:
                              intron_variant,coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
                              Validated:
                              by frequency
                              MAF:
                              T=0.00001/1 (GnomAD_exomes)
                              HGVS:
                              NC_000024.10:g.13335622G>T, NC_000024.9:g.15447502G>T, XM_011531455.4:c.2823C>A, XM_011531455.3:c.2823C>A, XM_011531455.2:c.2823C>A, XM_011531455.1:c.2823C>A, XM_011531453.4:c.2823C>A, XM_011531453.3:c.2823C>A, XM_011531453.2:c.2823C>A, XM_011531453.1:c.2823C>A, XM_011531454.4:c.2823C>A, XM_011531454.3:c.2823C>A, XM_011531454.2:c.2823C>A, XM_011531454.1:c.2823C>A, NM_007125.4:c.2484C>A, XM_011531441.4:c.2823C>A, XM_011531441.3:c.2823C>A, XM_011531441.2:c.2823C>A, XM_011531441.1:c.2823C>A, XM_011531442.4:c.2775C>A, XM_011531442.3:c.2775C>A, XM_011531442.2:c.2775C>A, XM_011531442.1:c.2775C>A, XM_011531443.4:c.2757C>A, XM_011531443.3:c.2757C>A, XM_011531443.2:c.2757C>A, XM_011531443.1:c.2757C>A, XM_011531445.4:c.2688C>A, XM_011531445.3:c.2688C>A, XM_011531445.2:c.2688C>A, XM_011531445.1:c.2688C>A, XM_011531446.4:c.2667C>A, XM_011531446.3:c.2667C>A, XM_011531446.2:c.2667C>A, XM_011531446.1:c.2667C>A, XM_011531447.4:c.2640C>A, XM_011531447.3:c.2640C>A, XM_011531447.2:c.2640C>A, XM_011531447.1:c.2640C>A, XM_011531448.4:c.2622C>A, XM_011531448.3:c.2622C>A, XM_011531448.2:c.2622C>A, XM_011531448.1:c.2622C>A, XM_011531451.4:c.2532C>A, XM_011531451.3:c.2532C>A, XM_011531451.2:c.2532C>A, XM_011531451.1:c.2532C>A, XM_011531459.4:c.2823C>A, XM_011531459.3:c.2823C>A, XM_011531459.2:c.2823C>A, XM_011531459.1:c.2823C>A, XM_011531460.4:c.2823C>A, XM_011531460.3:c.2823C>A, XM_011531460.2:c.2823C>A, XM_011531460.1:c.2823C>A, XM_017030070.3:c.2823C>A, XM_017030070.2:c.2823C>A, XM_017030070.1:c.2823C>A, XM_017030071.3:c.2823C>A, XM_017030071.2:c.2823C>A, XM_017030071.1:c.2823C>A, XM_017030073.3:c.2532C>A, XM_017030073.2:c.2532C>A, XM_017030073.1:c.2532C>A, NM_001258249.2:c.2775C>A, NM_001258249.1:c.2775C>A, XM_047442748.1:c.2775C>A, XM_047442749.1:c.2709C>A, XM_047442751.1:c.2667C>A, XM_047442752.1:c.2640C>A, XM_047442754.1:c.2619C>A, NR_047607.1:n.3835C>A, NR_047598.1:n.3725C>A, NR_047624.1:n.3709C>A, XM_047442747.1:c.2775C>A, NR_047645.1:n.3695C>A, XM_047442750.1:c.2688C>A, NR_047644.1:n.3682C>A, NM_001258258.1:c.2640C>A, NR_047599.1:n.3489C>A, NM_001258252.1:c.2619C>A, NM_001258261.1:c.2610C>A, NR_047603.1:n.3612C>A, NR_047597.1:n.3595C>A, NR_047642.1:n.3489C>A, NR_047618.1:n.3498C>A, NM_001258260.1:c.2574C>A, NM_001258264.1:c.2571C>A, NR_047637.1:n.3547C>A, NR_047641.1:n.3489C>A, NM_001258266.1:c.2619C>A, XM_047442753.1:c.2619C>A, NM_001258251.1:c.2532C>A, NM_001258267.1:c.2484C>A, NR_047602.1:n.3454C>A, NM_001258256.1:c.2619C>A, NR_047647.1:n.3446C>A, NM_001258259.1:c.2436C>A, NR_047600.1:n.3413C>A, NM_001258262.1:c.2403C>A, NR_047638.1:n.3555C>A, NM_001258253.1:c.2532C>A, NR_047646.1:n.3362C>A, NM_001258269.1:c.2337C>A, NM_001258263.1:c.2484C>A, NR_047635.1:n.3484C>A, NM_001258268.1:c.2247C>A, NR_047632.1:n.3197C>A, NM_001258255.1:c.2247C>A, NR_047609.1:n.3247C>A, NM_001258265.1:c.2235C>A, XM_047442746.1:c.2709C>A, NM_001258270.1:c.2112C>A, NM_001258257.1:c.2112C>A, NR_047643.1:n.3089C>A, NM_001258254.1:c.2247C>A, NM_001400177.1:c.2709C>A, NM_001258250.1:c.2064C>A, NM_001400175.1:c.2709C>A, NM_001400178.1:c.2619C>A, NR_047601.1:n.3089C>A, NM_001400181.1:c.2484C>A, NR_047627.1:n.2919C>A, NR_047604.1:n.2582C>A, NM_001400170.1:c.2619C>A, NM_001400171.1:c.2574C>A, NM_001400173.1:c.2484C>A, XM_047442755.1:c.2775C>A, NM_182659.1:c.2484C>A, XR_007068451.1:n.3828C>A, XM_047442756.1:c.2619C>A, XR_007068452.1:n.3780C>A, XM_047442757.1:c.2757C>A, NR_174405.1:n.2852C>A, NM_182660.1:c.2484C>A, NM_001400183.1:c.2775C>A, NM_001400185.1:c.2709C>A, NM_001400187.1:c.2667C>A, NM_001400189.1:c.2622C>A, NM_001400192.1:c.2619C>A, NM_001400195.1:c.2574C>A, NM_001400199.1:c.2532C>A

                              15.

                              rs1460686575 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>G [Show Flanks]
                                Chromosome:
                                Y:13479296 (GRCh38)
                                Y:15591176 (GRCh37)
                                Canonical SPDI:
                                NC_000024.10:13479295:C:G
                                Gene:
                                UTY (Varview), MIR12120 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,missense_variant,500B_downstream_variant,non_coding_transcript_variant,downstream_transcript_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.00001/1 (GnomAD_exomes)
                                HGVS:
                                NC_000024.10:g.13479296C>G, NC_000024.9:g.15591176C>G, XM_011531455.4:c.174G>C, XM_011531455.3:c.174G>C, XM_011531455.2:c.174G>C, XM_011531455.1:c.174G>C, XM_011531453.4:c.174G>C, XM_011531453.3:c.174G>C, XM_011531453.2:c.174G>C, XM_011531453.1:c.174G>C, XM_011531454.4:c.174G>C, XM_011531454.3:c.174G>C, XM_011531454.2:c.174G>C, XM_011531454.1:c.174G>C, NM_007125.4:c.174G>C, XM_011531441.4:c.174G>C, XM_011531441.3:c.174G>C, XM_011531441.2:c.174G>C, XM_011531441.1:c.174G>C, XM_011531442.4:c.174G>C, XM_011531442.3:c.174G>C, XM_011531442.2:c.174G>C, XM_011531442.1:c.174G>C, XM_011531443.4:c.174G>C, XM_011531443.3:c.174G>C, XM_011531443.2:c.174G>C, XM_011531443.1:c.174G>C, XM_011531445.4:c.174G>C, XM_011531445.3:c.174G>C, XM_011531445.2:c.174G>C, XM_011531445.1:c.174G>C, XM_011531446.4:c.174G>C, XM_011531446.3:c.174G>C, XM_011531446.2:c.174G>C, XM_011531446.1:c.174G>C, XM_011531447.4:c.174G>C, XM_011531447.3:c.174G>C, XM_011531447.2:c.174G>C, XM_011531447.1:c.174G>C, XM_011531448.4:c.174G>C, XM_011531448.3:c.174G>C, XM_011531448.2:c.174G>C, XM_011531448.1:c.174G>C, XM_011531451.4:c.174G>C, XM_011531451.3:c.174G>C, XM_011531451.2:c.174G>C, XM_011531451.1:c.174G>C, XM_011531459.4:c.174G>C, XM_011531459.3:c.174G>C, XM_011531459.2:c.174G>C, XM_011531459.1:c.174G>C, XM_011531460.4:c.174G>C, XM_011531460.3:c.174G>C, XM_011531460.2:c.174G>C, XM_011531460.1:c.174G>C, XM_017030070.3:c.174G>C, XM_017030070.2:c.174G>C, XM_017030070.1:c.174G>C, XM_017030071.3:c.174G>C, XM_017030071.2:c.174G>C, XM_017030071.1:c.174G>C, XM_017030073.3:c.174G>C, XM_017030073.2:c.174G>C, XM_017030073.1:c.174G>C, NM_001258249.2:c.174G>C, NM_001258249.1:c.174G>C, XM_047442748.1:c.174G>C, XM_047442749.1:c.174G>C, XM_047442751.1:c.174G>C, XM_047442752.1:c.174G>C, XM_047442754.1:c.174G>C, NR_047607.1:n.1179G>C, NR_047598.1:n.1179G>C, NR_047624.1:n.1179G>C, XM_047442747.1:c.174G>C, NR_047645.1:n.1179G>C, XM_047442750.1:c.174G>C, NR_047644.1:n.1179G>C, NM_001258258.1:c.174G>C, NR_047599.1:n.1179G>C, NM_001258252.1:c.174G>C, NM_001258261.1:c.174G>C, NR_047603.1:n.1179G>C, NR_047597.1:n.1179G>C, NR_047642.1:n.1179G>C, NR_047618.1:n.1179G>C, NM_001258260.1:c.174G>C, NM_001258264.1:c.174G>C, NR_047637.1:n.1179G>C, NR_047641.1:n.1179G>C, NM_001258266.1:c.174G>C, XM_047442753.1:c.174G>C, NM_001258251.1:c.174G>C, NM_001258267.1:c.174G>C, NR_047602.1:n.1179G>C, NM_001258256.1:c.174G>C, NR_047647.1:n.1179G>C, NM_001258259.1:c.174G>C, NR_047600.1:n.1179G>C, NM_001258262.1:c.174G>C, NR_047638.1:n.1179G>C, NM_001258253.1:c.174G>C, NR_047646.1:n.1179G>C, NM_001258269.1:c.174G>C, NM_001258263.1:c.174G>C, NR_047635.1:n.1179G>C, NM_001258268.1:c.174G>C, NR_047632.1:n.1179G>C, NM_001258255.1:c.174G>C, NR_047609.1:n.1179G>C, NM_001258265.1:c.174G>C, XM_047442746.1:c.174G>C, NM_001258270.1:c.174G>C, NM_001258257.1:c.174G>C, NR_047643.1:n.1179G>C, NM_001258254.1:c.174G>C, NM_001400177.1:c.174G>C, NM_001258250.1:c.174G>C, NR_047612.1:n.1179G>C, NM_001400175.1:c.174G>C, NM_001400178.1:c.174G>C, NR_047614.1:n.1179G>C, NR_047629.1:n.1179G>C, NR_047621.1:n.1179G>C, NR_047623.1:n.1179G>C, NR_047601.1:n.1179G>C, NR_047622.1:n.1179G>C, NR_047617.1:n.1179G>C, NR_047608.1:n.1179G>C, NR_047615.1:n.1179G>C, NR_047636.1:n.1179G>C, NR_047606.1:n.1179G>C, NR_047611.1:n.1179G>C, NR_047631.1:n.1179G>C, NR_047610.1:n.1179G>C, NR_047628.1:n.1179G>C, NM_001400181.1:c.174G>C, NR_047605.1:n.1179G>C, NR_047613.1:n.1179G>C, NR_047616.1:n.1179G>C, NR_047633.1:n.1179G>C, NR_047627.1:n.1179G>C, NR_047626.1:n.1179G>C, NR_047596.1:n.1179G>C, NR_047634.1:n.1179G>C, NR_047640.1:n.1179G>C, NR_047620.1:n.1179G>C, NR_047630.1:n.1179G>C, NR_047639.1:n.1179G>C, NR_047625.1:n.1179G>C, NR_047619.1:n.1179G>C, NR_047604.1:n.1179G>C, NM_001400170.1:c.174G>C, NM_001400171.1:c.174G>C, NM_001400173.1:c.174G>C, XM_047442755.1:c.174G>C, NM_182659.1:c.174G>C, XR_007068451.1:n.1179G>C, XM_047442756.1:c.174G>C, XR_007068452.1:n.1179G>C, NR_174404.1:n.542G>C, XM_047442757.1:c.174G>C, NR_174405.1:n.542G>C, NM_182660.1:c.174G>C, NM_001400183.1:c.174G>C, NM_001400185.1:c.174G>C, NM_001400187.1:c.174G>C, NM_001400189.1:c.174G>C, NM_001400192.1:c.174G>C, NM_001400195.1:c.174G>C, NM_001400199.1:c.174G>C, XP_011529757.1:p.Arg58Ser, XP_011529755.1:p.Arg58Ser, XP_011529756.1:p.Arg58Ser, NP_009056.3:p.Arg58Ser, XP_011529743.1:p.Arg58Ser, XP_011529744.1:p.Arg58Ser, XP_011529745.1:p.Arg58Ser, XP_011529747.1:p.Arg58Ser, XP_011529748.1:p.Arg58Ser, XP_011529749.1:p.Arg58Ser, XP_011529750.1:p.Arg58Ser, XP_011529753.1:p.Arg58Ser, XP_011529761.1:p.Arg58Ser, XP_011529762.1:p.Arg58Ser, XP_016885559.1:p.Arg58Ser, XP_016885560.1:p.Arg58Ser, XP_016885562.1:p.Arg58Ser, NP_001245178.1:p.Arg58Ser, XP_047298704.1:p.Arg58Ser, XP_047298705.1:p.Arg58Ser, XP_047298707.1:p.Arg58Ser, XP_047298708.1:p.Arg58Ser, XP_047298710.1:p.Arg58Ser, XP_047298703.1:p.Arg58Ser, XP_047298706.1:p.Arg58Ser, NP_001245187.1:p.Arg58Ser, NP_001245181.1:p.Arg58Ser, NP_001245190.1:p.Arg58Ser, NP_001245189.1:p.Arg58Ser, NP_001245193.1:p.Arg58Ser, NP_001245195.1:p.Arg58Ser, XP_047298709.1:p.Arg58Ser, NP_001245180.1:p.Arg58Ser, NP_001245196.1:p.Arg58Ser, NP_001245185.1:p.Arg58Ser, NP_001245188.1:p.Arg58Ser, NP_001245191.1:p.Arg58Ser, NP_001245182.1:p.Arg58Ser, NP_001245198.1:p.Arg58Ser, NP_001245192.1:p.Arg58Ser, NP_001245197.1:p.Arg58Ser, NP_001245184.1:p.Arg58Ser, NP_001245194.1:p.Arg58Ser, XP_047298702.1:p.Arg58Ser, NP_001245199.1:p.Arg58Ser, NP_001245186.1:p.Arg58Ser, NP_001245183.1:p.Arg58Ser, NP_001387106.1:p.Arg58Ser, NP_001245179.1:p.Arg58Ser, NP_001387104.1:p.Arg58Ser, NP_001387107.1:p.Arg58Ser, NP_001387110.1:p.Arg58Ser, NP_001387099.1:p.Arg58Ser, NP_001387100.1:p.Arg58Ser, NP_001387102.1:p.Arg58Ser, XP_047298711.1:p.Arg58Ser, NP_872600.1:p.Arg58Ser, XP_047298712.1:p.Arg58Ser, XP_047298713.1:p.Arg58Ser, NP_872601.1:p.Arg58Ser, NP_001387112.1:p.Arg58Ser, NP_001387114.1:p.Arg58Ser, NP_001387116.1:p.Arg58Ser, NP_001387118.1:p.Arg58Ser, NP_001387121.1:p.Arg58Ser, NP_001387124.1:p.Arg58Ser, NP_001387128.1:p.Arg58Ser

                                16.

                                rs1457277387 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  Y:13323722 (GRCh38)
                                  Y:15435602 (GRCh37)
                                  Canonical SPDI:
                                  NC_000024.10:13323721:T:C
                                  Gene:
                                  UTY (Varview)
                                  Functional Consequence:
                                  missense_variant,coding_sequence_variant,non_coding_transcript_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  C=0.00001/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000024.10:g.13323722T>C, NC_000024.9:g.15435602T>C, XM_011531455.4:c.3157A>G, XM_011531455.3:c.3157A>G, XM_011531455.2:c.3157A>G, XM_011531455.1:c.3157A>G, XM_011531453.4:c.3157A>G, XM_011531453.3:c.3157A>G, XM_011531453.2:c.3157A>G, XM_011531453.1:c.3157A>G, XM_011531454.4:c.3157A>G, XM_011531454.3:c.3157A>G, XM_011531454.2:c.3157A>G, XM_011531454.1:c.3157A>G, NM_007125.4:c.2818A>G, XM_011531441.4:c.3157A>G, XM_011531441.3:c.3157A>G, XM_011531441.2:c.3157A>G, XM_011531441.1:c.3157A>G, XM_011531442.4:c.3109A>G, XM_011531442.3:c.3109A>G, XM_011531442.2:c.3109A>G, XM_011531442.1:c.3109A>G, XM_011531443.4:c.3091A>G, XM_011531443.3:c.3091A>G, XM_011531443.2:c.3091A>G, XM_011531443.1:c.3091A>G, XM_011531445.4:c.3022A>G, XM_011531445.3:c.3022A>G, XM_011531445.2:c.3022A>G, XM_011531445.1:c.3022A>G, XM_011531446.4:c.3001A>G, XM_011531446.3:c.3001A>G, XM_011531446.2:c.3001A>G, XM_011531446.1:c.3001A>G, XM_011531447.4:c.2974A>G, XM_011531447.3:c.2974A>G, XM_011531447.2:c.2974A>G, XM_011531447.1:c.2974A>G, XM_011531448.4:c.2956A>G, XM_011531448.3:c.2956A>G, XM_011531448.2:c.2956A>G, XM_011531448.1:c.2956A>G, XM_011531451.4:c.2866A>G, XM_011531451.3:c.2866A>G, XM_011531451.2:c.2866A>G, XM_011531451.1:c.2866A>G, XM_011531459.4:c.3157A>G, XM_011531459.3:c.3157A>G, XM_011531459.2:c.3157A>G, XM_011531459.1:c.3157A>G, XM_011531460.4:c.3157A>G, XM_011531460.3:c.3157A>G, XM_011531460.2:c.3157A>G, XM_011531460.1:c.3157A>G, XM_017030070.3:c.3157A>G, XM_017030070.2:c.3157A>G, XM_017030070.1:c.3157A>G, XM_017030071.3:c.3157A>G, XM_017030071.2:c.3157A>G, XM_017030071.1:c.3157A>G, XM_017030073.3:c.2866A>G, XM_017030073.2:c.2866A>G, XM_017030073.1:c.2866A>G, NM_001258249.2:c.3109A>G, NM_001258249.1:c.3109A>G, XM_047442748.1:c.3109A>G, XM_047442749.1:c.3043A>G, XM_047442751.1:c.3001A>G, XM_047442752.1:c.2974A>G, XM_047442754.1:c.2953A>G, NR_047607.1:n.4169A>G, NR_047598.1:n.4059A>G, NR_047624.1:n.4043A>G, XM_047442747.1:c.3109A>G, NR_047645.1:n.4029A>G, XM_047442750.1:c.3022A>G, NR_047644.1:n.4016A>G, NM_001258258.1:c.2974A>G, NR_047599.1:n.3946A>G, NM_001258252.1:c.2953A>G, NM_001258261.1:c.2944A>G, NR_047603.1:n.3946A>G, NR_047597.1:n.3929A>G, NR_047642.1:n.3823A>G, NR_047618.1:n.3832A>G, NM_001258260.1:c.2908A>G, NM_001258264.1:c.2905A>G, NR_047637.1:n.3881A>G, NR_047641.1:n.3823A>G, NM_001258266.1:c.2953A>G, XM_047442753.1:c.2953A>G, NM_001258251.1:c.2866A>G, NM_001258267.1:c.2818A>G, NR_047602.1:n.3788A>G, NM_001258256.1:c.2953A>G, NR_047647.1:n.3780A>G, NM_001258259.1:c.2770A>G, NR_047600.1:n.3747A>G, NM_001258262.1:c.2737A>G, NR_047638.1:n.3889A>G, NM_001258253.1:c.2866A>G, NR_047646.1:n.3696A>G, NM_001258269.1:c.2671A>G, NM_001258263.1:c.2818A>G, NR_047635.1:n.3818A>G, NM_001258268.1:c.2581A>G, NR_047632.1:n.3531A>G, NM_001258255.1:c.2581A>G, NR_047609.1:n.3581A>G, NM_001258265.1:c.2569A>G, XM_047442746.1:c.3043A>G, NM_001258270.1:c.2446A>G, NM_001258257.1:c.2446A>G, NR_047643.1:n.3423A>G, NM_001258254.1:c.2581A>G, NM_001400177.1:c.3043A>G, NM_001258250.1:c.2398A>G, NR_047612.1:n.3341A>G, NM_001400175.1:c.3043A>G, NM_001400178.1:c.2953A>G, NR_047614.1:n.3254A>G, NR_047629.1:n.3050A>G, NR_047621.1:n.3290A>G, NR_047623.1:n.3185A>G, NR_047601.1:n.3423A>G, NR_047622.1:n.3242A>G, NR_047617.1:n.3190A>G, NR_047608.1:n.3137A>G, NR_047615.1:n.3108A>G, NR_047636.1:n.3188A>G, NR_047606.1:n.3186A>G, NR_047611.1:n.3185A>G, NR_047631.1:n.3050A>G, NR_047610.1:n.3050A>G, NR_047628.1:n.3098A>G, NM_001400181.1:c.2818A>G, NR_047605.1:n.3002A>G, NR_047613.1:n.3291A>G, NR_047616.1:n.3164A>G, NR_047633.1:n.3099A>G, NR_047627.1:n.3253A>G, NR_047626.1:n.3050A>G, NR_047596.1:n.3050A>G, NR_047634.1:n.3049A>G, NR_047640.1:n.3034A>G, NR_047620.1:n.3185A>G, NR_047630.1:n.3050A>G, NR_047639.1:n.2956A>G, NR_047625.1:n.2923A>G, NR_047619.1:n.3108A>G, NR_047604.1:n.2916A>G, NM_001400170.1:c.2953A>G, NM_001400171.1:c.2908A>G, NM_001400173.1:c.2818A>G, XM_047442755.1:c.3109A>G, NM_182659.1:c.2818A>G, XR_007068451.1:n.4162A>G, XM_047442756.1:c.2953A>G, XR_007068452.1:n.4114A>G, NR_174404.1:n.2569A>G, XM_047442757.1:c.3091A>G, NR_174405.1:n.3186A>G, NM_182660.1:c.2818A>G, NM_001400183.1:c.3109A>G, NM_001400185.1:c.3043A>G, NM_001400187.1:c.3001A>G, NM_001400189.1:c.2956A>G, NM_001400192.1:c.2953A>G, NM_001400195.1:c.2908A>G, NM_001400199.1:c.2866A>G, XP_011529757.1:p.Asn1053Asp, XP_011529755.1:p.Asn1053Asp, XP_011529756.1:p.Asn1053Asp, NP_009056.3:p.Asn940Asp, XP_011529743.1:p.Asn1053Asp, XP_011529744.1:p.Asn1037Asp, XP_011529745.1:p.Asn1031Asp, XP_011529747.1:p.Asn1008Asp, XP_011529748.1:p.Asn1001Asp, XP_011529749.1:p.Asn992Asp, XP_011529750.1:p.Asn986Asp, XP_011529753.1:p.Asn956Asp, XP_011529761.1:p.Asn1053Asp, XP_011529762.1:p.Asn1053Asp, XP_016885559.1:p.Asn1053Asp, XP_016885560.1:p.Asn1053Asp, XP_016885562.1:p.Asn956Asp, NP_001245178.1:p.Asn1037Asp, XP_047298704.1:p.Asn1037Asp, XP_047298705.1:p.Asn1015Asp, XP_047298707.1:p.Asn1001Asp, XP_047298708.1:p.Asn992Asp, XP_047298710.1:p.Asn985Asp, XP_047298703.1:p.Asn1037Asp, XP_047298706.1:p.Asn1008Asp, NP_001245187.1:p.Asn992Asp, NP_001245181.1:p.Asn985Asp, NP_001245190.1:p.Asn982Asp, NP_001245189.1:p.Asn970Asp, NP_001245193.1:p.Asn969Asp, NP_001245195.1:p.Asn985Asp, XP_047298709.1:p.Asn985Asp, NP_001245180.1:p.Asn956Asp, NP_001245196.1:p.Asn940Asp, NP_001245185.1:p.Asn985Asp, NP_001245188.1:p.Asn924Asp, NP_001245191.1:p.Asn913Asp, NP_001245182.1:p.Asn956Asp, NP_001245198.1:p.Asn891Asp, NP_001245192.1:p.Asn940Asp, NP_001245197.1:p.Asn861Asp, NP_001245184.1:p.Asn861Asp, NP_001245194.1:p.Asn857Asp, XP_047298702.1:p.Asn1015Asp, NP_001245199.1:p.Asn816Asp, NP_001245186.1:p.Asn816Asp, NP_001245183.1:p.Asn861Asp, NP_001387106.1:p.Asn1015Asp, NP_001245179.1:p.Asn800Asp, NP_001387104.1:p.Asn1015Asp, NP_001387107.1:p.Asn985Asp, NP_001387110.1:p.Asn940Asp, NP_001387099.1:p.Asn985Asp, NP_001387100.1:p.Asn970Asp, NP_001387102.1:p.Asn940Asp, XP_047298711.1:p.Asn1037Asp, NP_872600.1:p.Asn940Asp, XP_047298712.1:p.Asn985Asp, XP_047298713.1:p.Asn1031Asp, NP_872601.1:p.Asn940Asp, NP_001387112.1:p.Asn1037Asp, NP_001387114.1:p.Asn1015Asp, NP_001387116.1:p.Asn1001Asp, NP_001387118.1:p.Asn986Asp, NP_001387121.1:p.Asn985Asp, NP_001387124.1:p.Asn970Asp, NP_001387128.1:p.Asn956Asp

                                  17.

                                  rs1456132792 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A [Show Flanks]
                                    Chromosome:
                                    Y:13479286 (GRCh38)
                                    Y:15591166 (GRCh37)
                                    Canonical SPDI:
                                    NC_000024.10:13479285:C:A
                                    Gene:
                                    UTY (Varview), MIR12120 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant,500B_downstream_variant,non_coding_transcript_variant,downstream_transcript_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    A=0.00001/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000024.10:g.13479286C>A, NC_000024.9:g.15591166C>A, XM_011531455.4:c.184G>T, XM_011531455.3:c.184G>T, XM_011531455.2:c.184G>T, XM_011531455.1:c.184G>T, XM_011531453.4:c.184G>T, XM_011531453.3:c.184G>T, XM_011531453.2:c.184G>T, XM_011531453.1:c.184G>T, XM_011531454.4:c.184G>T, XM_011531454.3:c.184G>T, XM_011531454.2:c.184G>T, XM_011531454.1:c.184G>T, NM_007125.4:c.184G>T, XM_011531441.4:c.184G>T, XM_011531441.3:c.184G>T, XM_011531441.2:c.184G>T, XM_011531441.1:c.184G>T, XM_011531442.4:c.184G>T, XM_011531442.3:c.184G>T, XM_011531442.2:c.184G>T, XM_011531442.1:c.184G>T, XM_011531443.4:c.184G>T, XM_011531443.3:c.184G>T, XM_011531443.2:c.184G>T, XM_011531443.1:c.184G>T, XM_011531445.4:c.184G>T, XM_011531445.3:c.184G>T, XM_011531445.2:c.184G>T, XM_011531445.1:c.184G>T, XM_011531446.4:c.184G>T, XM_011531446.3:c.184G>T, XM_011531446.2:c.184G>T, XM_011531446.1:c.184G>T, XM_011531447.4:c.184G>T, XM_011531447.3:c.184G>T, XM_011531447.2:c.184G>T, XM_011531447.1:c.184G>T, XM_011531448.4:c.184G>T, XM_011531448.3:c.184G>T, XM_011531448.2:c.184G>T, XM_011531448.1:c.184G>T, XM_011531451.4:c.184G>T, XM_011531451.3:c.184G>T, XM_011531451.2:c.184G>T, XM_011531451.1:c.184G>T, XM_011531459.4:c.184G>T, XM_011531459.3:c.184G>T, XM_011531459.2:c.184G>T, XM_011531459.1:c.184G>T, XM_011531460.4:c.184G>T, XM_011531460.3:c.184G>T, XM_011531460.2:c.184G>T, XM_011531460.1:c.184G>T, XM_017030070.3:c.184G>T, XM_017030070.2:c.184G>T, XM_017030070.1:c.184G>T, XM_017030071.3:c.184G>T, XM_017030071.2:c.184G>T, XM_017030071.1:c.184G>T, XM_017030073.3:c.184G>T, XM_017030073.2:c.184G>T, XM_017030073.1:c.184G>T, NM_001258249.2:c.184G>T, NM_001258249.1:c.184G>T, XM_047442748.1:c.184G>T, XM_047442749.1:c.184G>T, XM_047442751.1:c.184G>T, XM_047442752.1:c.184G>T, XM_047442754.1:c.184G>T, NR_047607.1:n.1189G>T, NR_047598.1:n.1189G>T, NR_047624.1:n.1189G>T, XM_047442747.1:c.184G>T, NR_047645.1:n.1189G>T, XM_047442750.1:c.184G>T, NR_047644.1:n.1189G>T, NM_001258258.1:c.184G>T, NR_047599.1:n.1189G>T, NM_001258252.1:c.184G>T, NM_001258261.1:c.184G>T, NR_047603.1:n.1189G>T, NR_047597.1:n.1189G>T, NR_047642.1:n.1189G>T, NR_047618.1:n.1189G>T, NM_001258260.1:c.184G>T, NM_001258264.1:c.184G>T, NR_047637.1:n.1189G>T, NR_047641.1:n.1189G>T, NM_001258266.1:c.184G>T, XM_047442753.1:c.184G>T, NM_001258251.1:c.184G>T, NM_001258267.1:c.184G>T, NR_047602.1:n.1189G>T, NM_001258256.1:c.184G>T, NR_047647.1:n.1189G>T, NM_001258259.1:c.184G>T, NR_047600.1:n.1189G>T, NM_001258262.1:c.184G>T, NR_047638.1:n.1189G>T, NM_001258253.1:c.184G>T, NR_047646.1:n.1189G>T, NM_001258269.1:c.184G>T, NM_001258263.1:c.184G>T, NR_047635.1:n.1189G>T, NM_001258268.1:c.184G>T, NR_047632.1:n.1189G>T, NM_001258255.1:c.184G>T, NR_047609.1:n.1189G>T, NM_001258265.1:c.184G>T, XM_047442746.1:c.184G>T, NM_001258270.1:c.184G>T, NM_001258257.1:c.184G>T, NR_047643.1:n.1189G>T, NM_001258254.1:c.184G>T, NM_001400177.1:c.184G>T, NM_001258250.1:c.184G>T, NR_047612.1:n.1189G>T, NM_001400175.1:c.184G>T, NM_001400178.1:c.184G>T, NR_047614.1:n.1189G>T, NR_047629.1:n.1189G>T, NR_047621.1:n.1189G>T, NR_047623.1:n.1189G>T, NR_047601.1:n.1189G>T, NR_047622.1:n.1189G>T, NR_047617.1:n.1189G>T, NR_047608.1:n.1189G>T, NR_047615.1:n.1189G>T, NR_047636.1:n.1189G>T, NR_047606.1:n.1189G>T, NR_047611.1:n.1189G>T, NR_047631.1:n.1189G>T, NR_047610.1:n.1189G>T, NR_047628.1:n.1189G>T, NM_001400181.1:c.184G>T, NR_047605.1:n.1189G>T, NR_047613.1:n.1189G>T, NR_047616.1:n.1189G>T, NR_047633.1:n.1189G>T, NR_047627.1:n.1189G>T, NR_047626.1:n.1189G>T, NR_047596.1:n.1189G>T, NR_047634.1:n.1189G>T, NR_047640.1:n.1189G>T, NR_047620.1:n.1189G>T, NR_047630.1:n.1189G>T, NR_047639.1:n.1189G>T, NR_047625.1:n.1189G>T, NR_047619.1:n.1189G>T, NR_047604.1:n.1189G>T, NM_001400170.1:c.184G>T, NM_001400171.1:c.184G>T, NM_001400173.1:c.184G>T, XM_047442755.1:c.184G>T, NM_182659.1:c.184G>T, XR_007068451.1:n.1189G>T, XM_047442756.1:c.184G>T, XR_007068452.1:n.1189G>T, NR_174404.1:n.552G>T, XM_047442757.1:c.184G>T, NR_174405.1:n.552G>T, NM_182660.1:c.184G>T, NM_001400183.1:c.184G>T, NM_001400185.1:c.184G>T, NM_001400187.1:c.184G>T, NM_001400189.1:c.184G>T, NM_001400192.1:c.184G>T, NM_001400195.1:c.184G>T, NM_001400199.1:c.184G>T, XP_011529757.1:p.Asp62Tyr, XP_011529755.1:p.Asp62Tyr, XP_011529756.1:p.Asp62Tyr, NP_009056.3:p.Asp62Tyr, XP_011529743.1:p.Asp62Tyr, XP_011529744.1:p.Asp62Tyr, XP_011529745.1:p.Asp62Tyr, XP_011529747.1:p.Asp62Tyr, XP_011529748.1:p.Asp62Tyr, XP_011529749.1:p.Asp62Tyr, XP_011529750.1:p.Asp62Tyr, XP_011529753.1:p.Asp62Tyr, XP_011529761.1:p.Asp62Tyr, XP_011529762.1:p.Asp62Tyr, XP_016885559.1:p.Asp62Tyr, XP_016885560.1:p.Asp62Tyr, XP_016885562.1:p.Asp62Tyr, NP_001245178.1:p.Asp62Tyr, XP_047298704.1:p.Asp62Tyr, XP_047298705.1:p.Asp62Tyr, XP_047298707.1:p.Asp62Tyr, XP_047298708.1:p.Asp62Tyr, XP_047298710.1:p.Asp62Tyr, XP_047298703.1:p.Asp62Tyr, XP_047298706.1:p.Asp62Tyr, NP_001245187.1:p.Asp62Tyr, NP_001245181.1:p.Asp62Tyr, NP_001245190.1:p.Asp62Tyr, NP_001245189.1:p.Asp62Tyr, NP_001245193.1:p.Asp62Tyr, NP_001245195.1:p.Asp62Tyr, XP_047298709.1:p.Asp62Tyr, NP_001245180.1:p.Asp62Tyr, NP_001245196.1:p.Asp62Tyr, NP_001245185.1:p.Asp62Tyr, NP_001245188.1:p.Asp62Tyr, NP_001245191.1:p.Asp62Tyr, NP_001245182.1:p.Asp62Tyr, NP_001245198.1:p.Asp62Tyr, NP_001245192.1:p.Asp62Tyr, NP_001245197.1:p.Asp62Tyr, NP_001245184.1:p.Asp62Tyr, NP_001245194.1:p.Asp62Tyr, XP_047298702.1:p.Asp62Tyr, NP_001245199.1:p.Asp62Tyr, NP_001245186.1:p.Asp62Tyr, NP_001245183.1:p.Asp62Tyr, NP_001387106.1:p.Asp62Tyr, NP_001245179.1:p.Asp62Tyr, NP_001387104.1:p.Asp62Tyr, NP_001387107.1:p.Asp62Tyr, NP_001387110.1:p.Asp62Tyr, NP_001387099.1:p.Asp62Tyr, NP_001387100.1:p.Asp62Tyr, NP_001387102.1:p.Asp62Tyr, XP_047298711.1:p.Asp62Tyr, NP_872600.1:p.Asp62Tyr, XP_047298712.1:p.Asp62Tyr, XP_047298713.1:p.Asp62Tyr, NP_872601.1:p.Asp62Tyr, NP_001387112.1:p.Asp62Tyr, NP_001387114.1:p.Asp62Tyr, NP_001387116.1:p.Asp62Tyr, NP_001387118.1:p.Asp62Tyr, NP_001387121.1:p.Asp62Tyr, NP_001387124.1:p.Asp62Tyr, NP_001387128.1:p.Asp62Tyr

                                    18.

                                    rs1449703909 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      Y:13299055 (GRCh38)
                                      Y:15410935 (GRCh37)
                                      Canonical SPDI:
                                      NC_000024.10:13299054:C:T
                                      Gene:
                                      UTY (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,genic_downstream_transcript_variant,missense_variant,intron_variant,non_coding_transcript_variant,downstream_transcript_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      T=0.00002/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000024.10:g.13299055C>T, NC_000024.9:g.15410935C>T, XM_011531455.4:c.3818G>A, XM_011531455.3:c.3818G>A, XM_011531455.2:c.3818G>A, XM_011531455.1:c.3818G>A, XM_011531453.4:c.3818G>A, XM_011531453.3:c.3818G>A, XM_011531453.2:c.3818G>A, XM_011531453.1:c.3818G>A, XM_011531454.4:c.3818G>A, XM_011531454.3:c.3818G>A, XM_011531454.2:c.3818G>A, XM_011531454.1:c.3818G>A, NM_007125.4:c.3479G>A, XM_011531441.4:c.3818G>A, XM_011531441.3:c.3818G>A, XM_011531441.2:c.3818G>A, XM_011531441.1:c.3818G>A, XM_011531442.4:c.3770G>A, XM_011531442.3:c.3770G>A, XM_011531442.2:c.3770G>A, XM_011531442.1:c.3770G>A, XM_011531443.4:c.3752G>A, XM_011531443.3:c.3752G>A, XM_011531443.2:c.3752G>A, XM_011531443.1:c.3752G>A, XM_011531445.4:c.3683G>A, XM_011531445.3:c.3683G>A, XM_011531445.2:c.3683G>A, XM_011531445.1:c.3683G>A, XM_011531446.4:c.3662G>A, XM_011531446.3:c.3662G>A, XM_011531446.2:c.3662G>A, XM_011531446.1:c.3662G>A, XM_011531447.4:c.3635G>A, XM_011531447.3:c.3635G>A, XM_011531447.2:c.3635G>A, XM_011531447.1:c.3635G>A, XM_011531448.4:c.3617G>A, XM_011531448.3:c.3617G>A, XM_011531448.2:c.3617G>A, XM_011531448.1:c.3617G>A, XM_011531451.4:c.3527G>A, XM_011531451.3:c.3527G>A, XM_011531451.2:c.3527G>A, XM_011531451.1:c.3527G>A, XM_011531459.4:c.3818G>A, XM_011531459.3:c.3818G>A, XM_011531459.2:c.3818G>A, XM_011531459.1:c.3818G>A, NM_001258249.2:c.3770G>A, NM_001258249.1:c.3770G>A, XM_047442748.1:c.3770G>A, XM_047442749.1:c.3704G>A, XM_047442751.1:c.3662G>A, XM_047442752.1:c.3635G>A, XM_047442754.1:c.3614G>A, NR_047607.1:n.4830G>A, NR_047598.1:n.4788G>A, NR_047624.1:n.4704G>A, XM_047442747.1:c.3770G>A, NR_047645.1:n.4690G>A, XM_047442750.1:c.3683G>A, NR_047644.1:n.4677G>A, NM_001258258.1:c.3635G>A, NR_047599.1:n.4607G>A, NM_001258252.1:c.3614G>A, NM_001258261.1:c.3605G>A, NR_047603.1:n.4607G>A, NR_047597.1:n.4590G>A, NR_047642.1:n.4484G>A, NR_047618.1:n.4585G>A, NM_001258260.1:c.3569G>A, NM_001258264.1:c.3566G>A, NR_047637.1:n.4542G>A, NR_047641.1:n.4552G>A, NM_001258266.1:c.3539G>A, XM_047442753.1:c.3614G>A, NM_001258251.1:c.3527G>A, NM_001258267.1:c.3479G>A, NR_047602.1:n.4449G>A, NM_001258256.1:c.3614G>A, NR_047647.1:n.4441G>A, NM_001258259.1:c.3431G>A, NR_047600.1:n.4408G>A, NM_001258262.1:c.3398G>A, NR_047638.1:n.4550G>A, NM_001258253.1:c.3527G>A, NR_047646.1:n.4357G>A, NM_001258269.1:c.3332G>A, NM_001258263.1:c.3479G>A, NR_047635.1:n.4479G>A, NM_001258268.1:c.3242G>A, NR_047632.1:n.4260G>A, NM_001258255.1:c.3242G>A, NR_047609.1:n.4242G>A, NM_001258265.1:c.3230G>A, XM_047442746.1:c.3704G>A, NM_001258270.1:c.3107G>A, NM_001258257.1:c.3107G>A, NR_047643.1:n.4084G>A, NM_001258254.1:c.3242G>A, NM_001400177.1:c.3704G>A, NM_001258250.1:c.3059G>A, NR_047612.1:n.4002G>A, NM_001400175.1:c.3704G>A, NM_001400178.1:c.3614G>A, NR_047614.1:n.3983G>A, NR_047629.1:n.3978G>A, NR_047621.1:n.3951G>A, NR_047623.1:n.3914G>A, NR_047601.1:n.4084G>A, NR_047622.1:n.3903G>A, NR_047617.1:n.3880G>A, NR_047608.1:n.3866G>A, NR_047615.1:n.3837G>A, NR_047636.1:n.3849G>A, NR_047606.1:n.3847G>A, NR_047611.1:n.3846G>A, NR_047631.1:n.3803G>A, NR_047610.1:n.3779G>A, NR_047628.1:n.3759G>A, NM_001400181.1:c.3479G>A, NR_047605.1:n.3663G>A, NR_047616.1:n.3763G>A, NR_047633.1:n.3760G>A, NR_047626.1:n.3711G>A, NR_047596.1:n.3711G>A, NR_047634.1:n.3710G>A, NR_047640.1:n.3695G>A, NR_047620.1:n.3846G>A, NR_047630.1:n.3636G>A, NR_047639.1:n.3617G>A, NR_047625.1:n.3584G>A, NR_047619.1:n.3769G>A, NR_047604.1:n.3577G>A, NM_001400170.1:c.3614G>A, NM_001400171.1:c.3569G>A, NM_001400173.1:c.3479G>A, XM_047442755.1:c.3770G>A, NM_182659.1:c.3479G>A, NR_174404.1:n.3230G>A, NR_174405.1:n.3939G>A, XP_011529757.1:p.Arg1273Gln, XP_011529755.1:p.Arg1273Gln, XP_011529756.1:p.Arg1273Gln, NP_009056.3:p.Arg1160Gln, XP_011529743.1:p.Arg1273Gln, XP_011529744.1:p.Arg1257Gln, XP_011529745.1:p.Arg1251Gln, XP_011529747.1:p.Arg1228Gln, XP_011529748.1:p.Arg1221Gln, XP_011529749.1:p.Arg1212Gln, XP_011529750.1:p.Arg1206Gln, XP_011529753.1:p.Arg1176Gln, XP_011529761.1:p.Arg1273Gln, NP_001245178.1:p.Arg1257Gln, XP_047298704.1:p.Arg1257Gln, XP_047298705.1:p.Arg1235Gln, XP_047298707.1:p.Arg1221Gln, XP_047298708.1:p.Arg1212Gln, XP_047298710.1:p.Arg1205Gln, XP_047298703.1:p.Arg1257Gln, XP_047298706.1:p.Arg1228Gln, NP_001245187.1:p.Arg1212Gln, NP_001245181.1:p.Arg1205Gln, NP_001245190.1:p.Arg1202Gln, NP_001245189.1:p.Arg1190Gln, NP_001245193.1:p.Arg1189Gln, NP_001245195.1:p.Arg1180Gln, XP_047298709.1:p.Arg1205Gln, NP_001245180.1:p.Arg1176Gln, NP_001245196.1:p.Arg1160Gln, NP_001245185.1:p.Arg1205Gln, NP_001245188.1:p.Arg1144Gln, NP_001245191.1:p.Arg1133Gln, NP_001245182.1:p.Arg1176Gln, NP_001245198.1:p.Arg1111Gln, NP_001245192.1:p.Arg1160Gln, NP_001245197.1:p.Arg1081Gln, NP_001245184.1:p.Arg1081Gln, NP_001245194.1:p.Arg1077Gln, XP_047298702.1:p.Arg1235Gln, NP_001245199.1:p.Arg1036Gln, NP_001245186.1:p.Arg1036Gln, NP_001245183.1:p.Arg1081Gln, NP_001387106.1:p.Arg1235Gln, NP_001245179.1:p.Arg1020Gln, NP_001387104.1:p.Arg1235Gln, NP_001387107.1:p.Arg1205Gln, NP_001387110.1:p.Arg1160Gln, NP_001387099.1:p.Arg1205Gln, NP_001387100.1:p.Arg1190Gln, NP_001387102.1:p.Arg1160Gln, XP_047298711.1:p.Arg1257Gln, NP_872600.1:p.Arg1160Gln

                                      19.

                                      rs1445687317 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        Y:13360491 (GRCh38)
                                        Y:15472371 (GRCh37)
                                        Canonical SPDI:
                                        NC_000024.10:13360490:T:C
                                        Gene:
                                        UTY (Varview)
                                        Functional Consequence:
                                        missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0.00042/2 (ALFA)
                                        C=0.00003/2 (GnomAD_exomes)
                                        HGVS:
                                        NC_000024.10:g.13360491T>C, NC_000024.9:g.15472371T>C, XM_011531455.4:c.904A>G, XM_011531455.3:c.904A>G, XM_011531455.2:c.904A>G, XM_011531455.1:c.904A>G, XM_011531453.4:c.904A>G, XM_011531453.3:c.904A>G, XM_011531453.2:c.904A>G, XM_011531453.1:c.904A>G, XM_011531454.4:c.904A>G, XM_011531454.3:c.904A>G, XM_011531454.2:c.904A>G, XM_011531454.1:c.904A>G, NM_007125.4:c.904A>G, XM_011531441.4:c.904A>G, XM_011531441.3:c.904A>G, XM_011531441.2:c.904A>G, XM_011531441.1:c.904A>G, XM_011531442.4:c.904A>G, XM_011531442.3:c.904A>G, XM_011531442.2:c.904A>G, XM_011531442.1:c.904A>G, XM_011531443.4:c.904A>G, XM_011531443.3:c.904A>G, XM_011531443.2:c.904A>G, XM_011531443.1:c.904A>G, XM_011531445.4:c.904A>G, XM_011531445.3:c.904A>G, XM_011531445.2:c.904A>G, XM_011531445.1:c.904A>G, XM_011531446.4:c.904A>G, XM_011531446.3:c.904A>G, XM_011531446.2:c.904A>G, XM_011531446.1:c.904A>G, XM_011531447.4:c.904A>G, XM_011531447.3:c.904A>G, XM_011531447.2:c.904A>G, XM_011531447.1:c.904A>G, XM_011531448.4:c.904A>G, XM_011531448.3:c.904A>G, XM_011531448.2:c.904A>G, XM_011531448.1:c.904A>G, XM_011531451.4:c.904A>G, XM_011531451.3:c.904A>G, XM_011531451.2:c.904A>G, XM_011531451.1:c.904A>G, XM_011531459.4:c.904A>G, XM_011531459.3:c.904A>G, XM_011531459.2:c.904A>G, XM_011531459.1:c.904A>G, XM_011531460.4:c.904A>G, XM_011531460.3:c.904A>G, XM_011531460.2:c.904A>G, XM_011531460.1:c.904A>G, XM_017030070.3:c.904A>G, XM_017030070.2:c.904A>G, XM_017030070.1:c.904A>G, XM_017030071.3:c.904A>G, XM_017030071.2:c.904A>G, XM_017030071.1:c.904A>G, XM_017030073.3:c.904A>G, XM_017030073.2:c.904A>G, XM_017030073.1:c.904A>G, NM_001258249.2:c.904A>G, NM_001258249.1:c.904A>G, XM_047442748.1:c.904A>G, XM_047442749.1:c.904A>G, XM_047442751.1:c.904A>G, XM_047442752.1:c.904A>G, XM_047442754.1:c.904A>G, NR_047607.1:n.1909A>G, NR_047598.1:n.2010A>G, NR_047624.1:n.2129A>G, XM_047442747.1:c.904A>G, NR_047645.1:n.1980A>G, XM_047442750.1:c.904A>G, NR_047644.1:n.1909A>G, NM_001258258.1:c.904A>G, NR_047599.1:n.1909A>G, NM_001258252.1:c.904A>G, NR_047603.1:n.2032A>G, NR_047597.1:n.2015A>G, NR_047642.1:n.1909A>G, NR_047618.1:n.1909A>G, NM_001258260.1:c.904A>G, NR_047637.1:n.1909A>G, NR_047641.1:n.1909A>G, NM_001258266.1:c.904A>G, XM_047442753.1:c.904A>G, NM_001258251.1:c.904A>G, NM_001258267.1:c.904A>G, NR_047602.1:n.1874A>G, NM_001258256.1:c.904A>G, NR_047647.1:n.1909A>G, NR_047600.1:n.1874A>G, NM_001258262.1:c.904A>G, NR_047638.1:n.1975A>G, NM_001258253.1:c.904A>G, NR_047646.1:n.1782A>G, NM_001258269.1:c.904A>G, NM_001258263.1:c.904A>G, NR_047635.1:n.1904A>G, NM_001258268.1:c.904A>G, NR_047632.1:n.1989A>G, NM_001258255.1:c.904A>G, NR_047609.1:n.1909A>G, NM_001258265.1:c.655A>G, XM_047442746.1:c.904A>G, NM_001258270.1:c.904A>G, NM_001258257.1:c.904A>G, NR_047643.1:n.1909A>G, NM_001258254.1:c.904A>G, NM_001400177.1:c.904A>G, NR_047612.1:n.1909A>G, NM_001400175.1:c.904A>G, NM_001400178.1:c.904A>G, NR_047614.1:n.2023A>G, NR_047629.1:n.1909A>G, NR_047621.1:n.1980A>G, NR_047623.1:n.1909A>G, NR_047601.1:n.1909A>G, NR_047617.1:n.2015A>G, NR_047615.1:n.1909A>G, NR_047636.1:n.1909A>G, NR_047606.1:n.1909A>G, NR_047611.1:n.1909A>G, NR_047631.1:n.1909A>G, NR_047610.1:n.1909A>G, NR_047628.1:n.1909A>G, NM_001400181.1:c.904A>G, NR_047613.1:n.1859A>G, NR_047616.1:n.2023A>G, NR_047633.1:n.1909A>G, NR_047627.1:n.1874A>G, NR_047626.1:n.1909A>G, NR_047596.1:n.1909A>G, NR_047634.1:n.1874A>G, NR_047640.1:n.2015A>G, NR_047620.1:n.1909A>G, NR_047630.1:n.1909A>G, NR_047639.1:n.1815A>G, NR_047625.1:n.1782A>G, NR_047619.1:n.1909A>G, NR_047604.1:n.1909A>G, NM_001400170.1:c.904A>G, NM_001400171.1:c.904A>G, NM_001400173.1:c.904A>G, XM_047442755.1:c.904A>G, NM_182659.1:c.904A>G, XR_007068451.1:n.1909A>G, XM_047442756.1:c.904A>G, XR_007068452.1:n.1909A>G, NR_174404.1:n.1272A>G, XM_047442757.1:c.904A>G, NR_174405.1:n.1272A>G, NM_182660.1:c.904A>G, NM_001400183.1:c.904A>G, NM_001400185.1:c.904A>G, NM_001400187.1:c.904A>G, NM_001400189.1:c.904A>G, NM_001400192.1:c.904A>G, NM_001400195.1:c.904A>G, NM_001400199.1:c.904A>G, XP_011529757.1:p.Ile302Val, XP_011529755.1:p.Ile302Val, XP_011529756.1:p.Ile302Val, NP_009056.3:p.Ile302Val, XP_011529743.1:p.Ile302Val, XP_011529744.1:p.Ile302Val, XP_011529745.1:p.Ile302Val, XP_011529747.1:p.Ile302Val, XP_011529748.1:p.Ile302Val, XP_011529749.1:p.Ile302Val, XP_011529750.1:p.Ile302Val, XP_011529753.1:p.Ile302Val, XP_011529761.1:p.Ile302Val, XP_011529762.1:p.Ile302Val, XP_016885559.1:p.Ile302Val, XP_016885560.1:p.Ile302Val, XP_016885562.1:p.Ile302Val, NP_001245178.1:p.Ile302Val, XP_047298704.1:p.Ile302Val, XP_047298705.1:p.Ile302Val, XP_047298707.1:p.Ile302Val, XP_047298708.1:p.Ile302Val, XP_047298710.1:p.Ile302Val, XP_047298703.1:p.Ile302Val, XP_047298706.1:p.Ile302Val, NP_001245187.1:p.Ile302Val, NP_001245181.1:p.Ile302Val, NP_001245189.1:p.Ile302Val, NP_001245195.1:p.Ile302Val, XP_047298709.1:p.Ile302Val, NP_001245180.1:p.Ile302Val, NP_001245196.1:p.Ile302Val, NP_001245185.1:p.Ile302Val, NP_001245191.1:p.Ile302Val, NP_001245182.1:p.Ile302Val, NP_001245198.1:p.Ile302Val, NP_001245192.1:p.Ile302Val, NP_001245197.1:p.Ile302Val, NP_001245184.1:p.Ile302Val, NP_001245194.1:p.Ile219Val, XP_047298702.1:p.Ile302Val, NP_001245199.1:p.Ile302Val, NP_001245186.1:p.Ile302Val, NP_001245183.1:p.Ile302Val, NP_001387106.1:p.Ile302Val, NP_001387104.1:p.Ile302Val, NP_001387107.1:p.Ile302Val, NP_001387110.1:p.Ile302Val, NP_001387099.1:p.Ile302Val, NP_001387100.1:p.Ile302Val, NP_001387102.1:p.Ile302Val, XP_047298711.1:p.Ile302Val, NP_872600.1:p.Ile302Val, XP_047298712.1:p.Ile302Val, XP_047298713.1:p.Ile302Val, NP_872601.1:p.Ile302Val, NP_001387112.1:p.Ile302Val, NP_001387114.1:p.Ile302Val, NP_001387116.1:p.Ile302Val, NP_001387118.1:p.Ile302Val, NP_001387121.1:p.Ile302Val, NP_001387124.1:p.Ile302Val, NP_001387128.1:p.Ile302Val

                                        20.

                                        rs1437599600 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>C [Show Flanks]
                                          Chromosome:
                                          Y:13335951 (GRCh38)
                                          Y:15447831 (GRCh37)
                                          Canonical SPDI:
                                          NC_000024.10:13335950:A:C
                                          Gene:
                                          UTY (Varview)
                                          Functional Consequence:
                                          missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          C=0.00001/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000024.10:g.13335951A>C, NC_000024.9:g.15447831A>C, XM_011531455.4:c.2494T>G, XM_011531455.3:c.2494T>G, XM_011531455.2:c.2494T>G, XM_011531455.1:c.2494T>G, XM_011531453.4:c.2494T>G, XM_011531453.3:c.2494T>G, XM_011531453.2:c.2494T>G, XM_011531453.1:c.2494T>G, XM_011531454.4:c.2494T>G, XM_011531454.3:c.2494T>G, XM_011531454.2:c.2494T>G, XM_011531454.1:c.2494T>G, NM_007125.4:c.2155T>G, XM_011531441.4:c.2494T>G, XM_011531441.3:c.2494T>G, XM_011531441.2:c.2494T>G, XM_011531441.1:c.2494T>G, XM_011531442.4:c.2446T>G, XM_011531442.3:c.2446T>G, XM_011531442.2:c.2446T>G, XM_011531442.1:c.2446T>G, XM_011531443.4:c.2428T>G, XM_011531443.3:c.2428T>G, XM_011531443.2:c.2428T>G, XM_011531443.1:c.2428T>G, XM_011531445.4:c.2359T>G, XM_011531445.3:c.2359T>G, XM_011531445.2:c.2359T>G, XM_011531445.1:c.2359T>G, XM_011531446.4:c.2338T>G, XM_011531446.3:c.2338T>G, XM_011531446.2:c.2338T>G, XM_011531446.1:c.2338T>G, XM_011531447.4:c.2311T>G, XM_011531447.3:c.2311T>G, XM_011531447.2:c.2311T>G, XM_011531447.1:c.2311T>G, XM_011531448.4:c.2293T>G, XM_011531448.3:c.2293T>G, XM_011531448.2:c.2293T>G, XM_011531448.1:c.2293T>G, XM_011531451.4:c.2203T>G, XM_011531451.3:c.2203T>G, XM_011531451.2:c.2203T>G, XM_011531451.1:c.2203T>G, XM_011531459.4:c.2494T>G, XM_011531459.3:c.2494T>G, XM_011531459.2:c.2494T>G, XM_011531459.1:c.2494T>G, XM_011531460.4:c.2494T>G, XM_011531460.3:c.2494T>G, XM_011531460.2:c.2494T>G, XM_011531460.1:c.2494T>G, XM_017030070.3:c.2494T>G, XM_017030070.2:c.2494T>G, XM_017030070.1:c.2494T>G, XM_017030071.3:c.2494T>G, XM_017030071.2:c.2494T>G, XM_017030071.1:c.2494T>G, XM_017030073.3:c.2203T>G, XM_017030073.2:c.2203T>G, XM_017030073.1:c.2203T>G, NM_001258249.2:c.2446T>G, NM_001258249.1:c.2446T>G, XM_047442748.1:c.2446T>G, XM_047442749.1:c.2380T>G, XM_047442751.1:c.2338T>G, XM_047442752.1:c.2311T>G, XM_047442754.1:c.2290T>G, NR_047607.1:n.3506T>G, NR_047598.1:n.3396T>G, NR_047624.1:n.3380T>G, XM_047442747.1:c.2446T>G, NR_047645.1:n.3366T>G, XM_047442750.1:c.2359T>G, NR_047644.1:n.3353T>G, NM_001258258.1:c.2311T>G, NR_047599.1:n.3160T>G, NM_001258252.1:c.2290T>G, NM_001258261.1:c.2281T>G, NR_047603.1:n.3283T>G, NR_047597.1:n.3266T>G, NR_047642.1:n.3160T>G, NR_047618.1:n.3169T>G, NM_001258260.1:c.2245T>G, NM_001258264.1:c.2242T>G, NR_047637.1:n.3218T>G, NR_047641.1:n.3160T>G, NM_001258266.1:c.2290T>G, XM_047442753.1:c.2290T>G, NM_001258251.1:c.2203T>G, NM_001258267.1:c.2155T>G, NR_047602.1:n.3125T>G, NM_001258256.1:c.2290T>G, NR_047647.1:n.3117T>G, NM_001258259.1:c.2107T>G, NR_047600.1:n.3084T>G, NM_001258262.1:c.2074T>G, NR_047638.1:n.3226T>G, NM_001258253.1:c.2203T>G, NR_047646.1:n.3033T>G, NM_001258269.1:c.2008T>G, NM_001258263.1:c.2155T>G, NR_047635.1:n.3155T>G, NM_001258268.1:c.1918T>G, NR_047632.1:n.2868T>G, NM_001258255.1:c.1918T>G, NR_047609.1:n.2918T>G, NM_001258265.1:c.1906T>G, XM_047442746.1:c.2380T>G, NM_001258270.1:c.1783T>G, NM_001258257.1:c.1783T>G, NM_001258254.1:c.1918T>G, NM_001400177.1:c.2380T>G, NM_001258250.1:c.1735T>G, NM_001400175.1:c.2380T>G, NM_001400178.1:c.2290T>G, NM_001400181.1:c.2155T>G, NM_001400170.1:c.2290T>G, NM_001400171.1:c.2245T>G, NM_001400173.1:c.2155T>G, XM_047442755.1:c.2446T>G, NM_182659.1:c.2155T>G, XR_007068451.1:n.3499T>G, XM_047442756.1:c.2290T>G, XR_007068452.1:n.3451T>G, XM_047442757.1:c.2428T>G, NR_174405.1:n.2523T>G, NM_182660.1:c.2155T>G, NM_001400183.1:c.2446T>G, NM_001400185.1:c.2380T>G, NM_001400187.1:c.2338T>G, NM_001400189.1:c.2293T>G, NM_001400192.1:c.2290T>G, NM_001400195.1:c.2245T>G, NM_001400199.1:c.2203T>G, XP_011529757.1:p.Leu832Val, XP_011529755.1:p.Leu832Val, XP_011529756.1:p.Leu832Val, NP_009056.3:p.Leu719Val, XP_011529743.1:p.Leu832Val, XP_011529744.1:p.Leu816Val, XP_011529745.1:p.Leu810Val, XP_011529747.1:p.Leu787Val, XP_011529748.1:p.Leu780Val, XP_011529749.1:p.Leu771Val, XP_011529750.1:p.Leu765Val, XP_011529753.1:p.Leu735Val, XP_011529761.1:p.Leu832Val, XP_011529762.1:p.Leu832Val, XP_016885559.1:p.Leu832Val, XP_016885560.1:p.Leu832Val, XP_016885562.1:p.Leu735Val, NP_001245178.1:p.Leu816Val, XP_047298704.1:p.Leu816Val, XP_047298705.1:p.Leu794Val, XP_047298707.1:p.Leu780Val, XP_047298708.1:p.Leu771Val, XP_047298710.1:p.Leu764Val, XP_047298703.1:p.Leu816Val, XP_047298706.1:p.Leu787Val, NP_001245187.1:p.Leu771Val, NP_001245181.1:p.Leu764Val, NP_001245190.1:p.Leu761Val, NP_001245189.1:p.Leu749Val, NP_001245193.1:p.Leu748Val, NP_001245195.1:p.Leu764Val, XP_047298709.1:p.Leu764Val, NP_001245180.1:p.Leu735Val, NP_001245196.1:p.Leu719Val, NP_001245185.1:p.Leu764Val, NP_001245188.1:p.Leu703Val, NP_001245191.1:p.Leu692Val, NP_001245182.1:p.Leu735Val, NP_001245198.1:p.Leu670Val, NP_001245192.1:p.Leu719Val, NP_001245197.1:p.Leu640Val, NP_001245184.1:p.Leu640Val, NP_001245194.1:p.Leu636Val, XP_047298702.1:p.Leu794Val, NP_001245199.1:p.Leu595Val, NP_001245186.1:p.Leu595Val, NP_001245183.1:p.Leu640Val, NP_001387106.1:p.Leu794Val, NP_001245179.1:p.Leu579Val, NP_001387104.1:p.Leu794Val, NP_001387107.1:p.Leu764Val, NP_001387110.1:p.Leu719Val, NP_001387099.1:p.Leu764Val, NP_001387100.1:p.Leu749Val, NP_001387102.1:p.Leu719Val, XP_047298711.1:p.Leu816Val, NP_872600.1:p.Leu719Val, XP_047298712.1:p.Leu764Val, XP_047298713.1:p.Leu810Val, NP_872601.1:p.Leu719Val, NP_001387112.1:p.Leu816Val, NP_001387114.1:p.Leu794Val, NP_001387116.1:p.Leu780Val, NP_001387118.1:p.Leu765Val, NP_001387121.1:p.Leu764Val, NP_001387124.1:p.Leu749Val, NP_001387128.1:p.Leu735Val

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