U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 796

1.

rs1489221730 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G [Show Flanks]
    Chromosome:
    X:152918127 (GRCh38)
    X:152086671 (GRCh37)
    Canonical SPDI:
    NC_000023.11:152918126:A:C,NC_000023.11:152918126:A:G
    Gene:
    ZNF185 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,5_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000007/1 (GnomAD_exomes)
    C=0.00001/1 (GnomAD)
    HGVS:
    NC_000023.11:g.152918127A>C, NC_000023.11:g.152918127A>G, NW_003871103.3:g.352110A>C, NW_003871103.3:g.352110A>G, NG_021255.2:g.8686A>C, NG_021255.2:g.8686A>G, NM_007150.3:c.404A>C, NM_007150.3:c.404A>G, NM_001178108.2:c.404A>C, NM_001178108.2:c.404A>G, NM_001178108.1:c.404A>C, NM_001178108.1:c.404A>G, NM_001388432.2:c.404A>C, NM_001388432.2:c.404A>G, NM_001388432.1:c.404A>C, NM_001388432.1:c.404A>G, NM_001178113.2:c.-2A>C, NM_001178113.2:c.-2A>G, NM_001178113.1:c.-2A>C, NM_001178113.1:c.-2A>G, NM_001178106.1:c.404A>C, NM_001178106.1:c.404A>G, NM_001395254.1:c.404A>C, NM_001395254.1:c.404A>G, NM_001178107.1:c.404A>C, NM_001178107.1:c.404A>G, NM_001178109.1:c.404A>C, NM_001178109.1:c.404A>G, NM_001178110.1:c.404A>C, NM_001178110.1:c.404A>G, NW_025791818.1:g.533317A>C, NW_025791818.1:g.533317A>G, NC_000023.10:g.152086671A>C, NC_000023.10:g.152086671A>G, XM_005274746.4:c.404A>C, XM_005274746.4:c.404A>G, XM_005274746.3:c.404A>C, XM_005274746.3:c.404A>G, XM_005274746.2:c.404A>C, XM_005274746.2:c.404A>G, XM_005274746.1:c.404A>C, XM_005274746.1:c.404A>G, XM_017029822.3:c.404A>C, XM_017029822.3:c.404A>G, XM_017029822.2:c.404A>C, XM_017029822.2:c.404A>G, XM_017029822.1:c.404A>C, XM_017029822.1:c.404A>G, XM_005274738.3:c.404A>C, XM_005274738.3:c.404A>G, XM_005274738.2:c.404A>C, XM_005274738.2:c.404A>G, XM_005274738.1:c.404A>C, XM_005274738.1:c.404A>G, XM_005274741.3:c.404A>C, XM_005274741.3:c.404A>G, XM_005274741.2:c.404A>C, XM_005274741.2:c.404A>G, XM_005274741.1:c.404A>C, XM_005274741.1:c.404A>G, XM_005274740.3:c.404A>C, XM_005274740.3:c.404A>G, XM_005274740.2:c.404A>C, XM_005274740.2:c.404A>G, XM_005274740.1:c.404A>C, XM_005274740.1:c.404A>G, XM_005274742.3:c.404A>C, XM_005274742.3:c.404A>G, XM_005274742.2:c.404A>C, XM_005274742.2:c.404A>G, XM_005274742.1:c.404A>C, XM_005274742.1:c.404A>G, XM_005274744.3:c.404A>C, XM_005274744.3:c.404A>G, XM_005274744.2:c.404A>C, XM_005274744.2:c.404A>G, XM_005274744.1:c.404A>C, XM_005274744.1:c.404A>G, XM_005274745.3:c.404A>C, XM_005274745.3:c.404A>G, XM_005274745.2:c.404A>C, XM_005274745.2:c.404A>G, XM_005274745.1:c.404A>C, XM_005274745.1:c.404A>G, XM_017029821.2:c.404A>C, XM_017029821.2:c.404A>G, XM_017029821.1:c.404A>C, XM_017029821.1:c.404A>G, XM_017029823.2:c.404A>C, XM_017029823.2:c.404A>G, XM_017029823.1:c.404A>C, XM_017029823.1:c.404A>G, XM_017029824.2:c.404A>C, XM_017029824.2:c.404A>G, XM_017029824.1:c.404A>C, XM_017029824.1:c.404A>G, XM_017029825.2:c.404A>C, XM_017029825.2:c.404A>G, XM_017029825.1:c.404A>C, XM_017029825.1:c.404A>G, XM_017029826.2:c.404A>C, XM_017029826.2:c.404A>G, XM_017029826.1:c.404A>C, XM_017029826.1:c.404A>G, XM_017029827.2:c.404A>C, XM_017029827.2:c.404A>G, XM_017029827.1:c.404A>C, XM_017029827.1:c.404A>G, XM_017029828.2:c.404A>C, XM_017029828.2:c.404A>G, XM_017029828.1:c.404A>C, XM_017029828.1:c.404A>G, XM_017029829.2:c.404A>C, XM_017029829.2:c.404A>G, XM_017029829.1:c.404A>C, XM_017029829.1:c.404A>G, XM_017029830.2:c.404A>C, XM_017029830.2:c.404A>G, XM_017029830.1:c.404A>C, XM_017029830.1:c.404A>G, XM_017029831.2:c.404A>C, XM_017029831.2:c.404A>G, XM_017029831.1:c.404A>C, XM_017029831.1:c.404A>G, XM_017029832.2:c.404A>C, XM_017029832.2:c.404A>G, XM_017029832.1:c.404A>C, XM_017029832.1:c.404A>G, XM_017029833.2:c.404A>C, XM_017029833.2:c.404A>G, XM_017029833.1:c.404A>C, XM_017029833.1:c.404A>G, XM_017029834.2:c.404A>C, XM_017029834.2:c.404A>G, XM_017029834.1:c.404A>C, XM_017029834.1:c.404A>G, XM_017029835.2:c.404A>C, XM_017029835.2:c.404A>G, XM_017029835.1:c.404A>C, XM_017029835.1:c.404A>G, XM_011531194.2:c.404A>C, XM_011531194.2:c.404A>G, XM_011531194.1:c.404A>C, XM_011531194.1:c.404A>G, XM_011531195.2:c.404A>C, XM_011531195.2:c.404A>G, XM_011531195.1:c.404A>C, XM_011531195.1:c.404A>G, XM_047442492.1:c.404A>C, XM_047442492.1:c.404A>G, XM_047442493.1:c.404A>C, XM_047442493.1:c.404A>G, XM_047442495.1:c.404A>C, XM_047442495.1:c.404A>G, XM_047442497.1:c.404A>C, XM_047442497.1:c.404A>G, XM_047442498.1:c.404A>C, XM_047442498.1:c.404A>G, XM_047442499.1:c.404A>C, XM_047442499.1:c.404A>G, XM_047442500.1:c.404A>C, XM_047442500.1:c.404A>G, XM_047442503.1:c.404A>C, XM_047442503.1:c.404A>G, XM_047442505.1:c.404A>C, XM_047442505.1:c.404A>G, XM_047442504.1:c.404A>C, XM_047442504.1:c.404A>G, XM_047442506.1:c.404A>C, XM_047442506.1:c.404A>G, XM_047442507.1:c.404A>C, XM_047442507.1:c.404A>G, XM_047442508.1:c.404A>C, XM_047442508.1:c.404A>G, XM_047442509.1:c.404A>C, XM_047442509.1:c.404A>G, NM_001178114.1:c.-34A>C, NM_001178114.1:c.-34A>G, XM_047442494.1:c.404A>C, XM_047442494.1:c.404A>G, XM_047442491.1:c.404A>C, XM_047442491.1:c.404A>G, XM_047442502.1:c.404A>C, XM_047442502.1:c.404A>G, XM_047442501.1:c.404A>C, XM_047442501.1:c.404A>G, XM_047442488.1:c.404A>C, XM_047442488.1:c.404A>G, XM_047442489.1:c.404A>C, XM_047442489.1:c.404A>G, XM_047442490.1:c.404A>C, XM_047442490.1:c.404A>G, XM_047442496.1:c.404A>C, XM_047442496.1:c.404A>G, NP_009081.2:p.Lys135Thr, NP_009081.2:p.Lys135Arg, NP_001171579.1:p.Lys135Thr, NP_001171579.1:p.Lys135Arg, NP_001375361.1:p.Lys135Thr, NP_001375361.1:p.Lys135Arg, NP_001171577.1:p.Lys135Thr, NP_001171577.1:p.Lys135Arg, NP_001382183.1:p.Lys135Thr, NP_001382183.1:p.Lys135Arg, NP_001171578.1:p.Lys135Thr, NP_001171578.1:p.Lys135Arg, NP_001171580.1:p.Lys135Thr, NP_001171580.1:p.Lys135Arg, NP_001171581.1:p.Lys135Thr, NP_001171581.1:p.Lys135Arg, XP_005274803.1:p.Lys135Thr, XP_005274803.1:p.Lys135Arg, XP_016885311.1:p.Lys135Thr, XP_016885311.1:p.Lys135Arg, XP_005274795.1:p.Lys135Thr, XP_005274795.1:p.Lys135Arg, XP_005274798.1:p.Lys135Thr, XP_005274798.1:p.Lys135Arg, XP_005274797.1:p.Lys135Thr, XP_005274797.1:p.Lys135Arg, XP_005274799.1:p.Lys135Thr, XP_005274799.1:p.Lys135Arg, XP_005274801.1:p.Lys135Thr, XP_005274801.1:p.Lys135Arg, XP_005274802.1:p.Lys135Thr, XP_005274802.1:p.Lys135Arg, XP_016885310.1:p.Lys135Thr, XP_016885310.1:p.Lys135Arg, XP_016885312.1:p.Lys135Thr, XP_016885312.1:p.Lys135Arg, XP_016885313.1:p.Lys135Thr, XP_016885313.1:p.Lys135Arg, XP_016885314.1:p.Lys135Thr, XP_016885314.1:p.Lys135Arg, XP_016885315.1:p.Lys135Thr, XP_016885315.1:p.Lys135Arg, XP_016885316.1:p.Lys135Thr, XP_016885316.1:p.Lys135Arg, XP_016885317.1:p.Lys135Thr, XP_016885317.1:p.Lys135Arg, XP_016885318.1:p.Lys135Thr, XP_016885318.1:p.Lys135Arg, XP_016885319.1:p.Lys135Thr, XP_016885319.1:p.Lys135Arg, XP_016885320.1:p.Lys135Thr, XP_016885320.1:p.Lys135Arg, XP_016885321.1:p.Lys135Thr, XP_016885321.1:p.Lys135Arg, XP_016885322.1:p.Lys135Thr, XP_016885322.1:p.Lys135Arg, XP_016885323.1:p.Lys135Thr, XP_016885323.1:p.Lys135Arg, XP_016885324.1:p.Lys135Thr, XP_016885324.1:p.Lys135Arg, XP_011529496.1:p.Lys135Thr, XP_011529496.1:p.Lys135Arg, XP_011529497.1:p.Lys135Thr, XP_011529497.1:p.Lys135Arg, XP_047298448.1:p.Lys135Thr, XP_047298448.1:p.Lys135Arg, XP_047298449.1:p.Lys135Thr, XP_047298449.1:p.Lys135Arg, XP_047298451.1:p.Lys135Thr, XP_047298451.1:p.Lys135Arg, XP_047298453.1:p.Lys135Thr, XP_047298453.1:p.Lys135Arg, XP_047298454.1:p.Lys135Thr, XP_047298454.1:p.Lys135Arg, XP_047298455.1:p.Lys135Thr, XP_047298455.1:p.Lys135Arg, XP_047298456.1:p.Lys135Thr, XP_047298456.1:p.Lys135Arg, XP_047298459.1:p.Lys135Thr, XP_047298459.1:p.Lys135Arg, XP_047298461.1:p.Lys135Thr, XP_047298461.1:p.Lys135Arg, XP_047298460.1:p.Lys135Thr, XP_047298460.1:p.Lys135Arg, XP_047298462.1:p.Lys135Thr, XP_047298462.1:p.Lys135Arg, XP_047298463.1:p.Lys135Thr, XP_047298463.1:p.Lys135Arg, XP_047298464.1:p.Lys135Thr, XP_047298464.1:p.Lys135Arg, XP_047298465.1:p.Lys135Thr, XP_047298465.1:p.Lys135Arg, XP_047298450.1:p.Lys135Thr, XP_047298450.1:p.Lys135Arg, XP_047298447.1:p.Lys135Thr, XP_047298447.1:p.Lys135Arg, XP_047298458.1:p.Lys135Thr, XP_047298458.1:p.Lys135Arg, XP_047298457.1:p.Lys135Thr, XP_047298457.1:p.Lys135Arg, XP_047298444.1:p.Lys135Thr, XP_047298444.1:p.Lys135Arg, XP_047298445.1:p.Lys135Thr, XP_047298445.1:p.Lys135Arg, XP_047298446.1:p.Lys135Thr, XP_047298446.1:p.Lys135Arg, XP_047298452.1:p.Lys135Thr, XP_047298452.1:p.Lys135Arg

    2.

    rs1488273772 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      X:152973323 (GRCh38)
      X:152141867 (GRCh37)
      Canonical SPDI:
      NC_000023.11:152973322:C:T
      Gene:
      ZNF185 (Varview)
      Functional Consequence:
      3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0./0 (ALFA)
      T=0.000008/2 (TOPMED)
      T=0.000019/2 (GnomAD)
      HGVS:
      NC_000023.11:g.152973323C>T, NW_003871103.3:g.407306C>T, NG_021255.2:g.63882C>T, NM_007150.3:c.*2050C>T, NM_001178108.2:c.*2050C>T, NM_001178108.1:c.*2050C>T, NM_001388432.2:c.*2050C>T, NM_001388432.1:c.*2050C>T, NM_001178113.2:c.*2050C>T, NM_001178113.1:c.*2050C>T, NM_001178115.2:c.*2050C>T, NM_001178115.1:c.*2050C>T, NM_001178106.1:c.*2050C>T, NM_001395254.1:c.*2050C>T, NM_001178107.1:c.*2050C>T, NM_001178109.1:c.*2050C>T, NM_001178110.1:c.*2050C>T, NW_025791818.1:g.588513C>T, NC_000023.10:g.152141867C>T, XM_005274746.4:c.*2050C>T, XM_005274746.3:c.*2050C>T, XM_005274746.2:c.*2050C>T, XM_005274746.1:c.*2050C>T, XM_017029822.3:c.*2050C>T, XM_017029822.2:c.*2050C>T, XM_017029822.1:c.*2050C>T, XM_005274738.3:c.*2050C>T, XM_005274738.2:c.*2050C>T, XM_005274738.1:c.*2050C>T, XM_005274741.3:c.*2050C>T, XM_005274741.2:c.*2050C>T, XM_005274741.1:c.*2050C>T, XM_005274740.3:c.*2050C>T, XM_005274740.2:c.*2050C>T, XM_005274740.1:c.*2050C>T, XM_005274742.3:c.*2050C>T, XM_005274742.2:c.*2050C>T, XM_005274742.1:c.*2050C>T, XM_005274744.3:c.*2050C>T, XM_005274744.2:c.*2050C>T, XM_005274744.1:c.*2050C>T, XM_005274745.3:c.*2050C>T, XM_005274745.2:c.*2050C>T, XM_005274745.1:c.*2050C>T, XM_017029821.2:c.*2050C>T, XM_017029821.1:c.*2050C>T, XM_017029823.2:c.*2050C>T, XM_017029823.1:c.*2050C>T, XM_017029824.2:c.*2050C>T, XM_017029824.1:c.*2050C>T, XM_017029825.2:c.*2050C>T, XM_017029825.1:c.*2050C>T, XM_017029826.2:c.*2050C>T, XM_017029826.1:c.*2050C>T, XM_017029827.2:c.*2050C>T, XM_017029827.1:c.*2050C>T, XM_017029828.2:c.*2050C>T, XM_017029828.1:c.*2050C>T, XM_017029829.2:c.*2050C>T, XM_017029829.1:c.*2050C>T, XM_017029830.2:c.*2050C>T, XM_017029830.1:c.*2050C>T, XM_017029831.2:c.*2050C>T, XM_017029831.1:c.*2050C>T, XM_017029832.2:c.*2050C>T, XM_017029832.1:c.*2050C>T, XM_017029833.2:c.*2050C>T, XM_017029833.1:c.*2050C>T, XM_017029834.2:c.*2050C>T, XM_017029834.1:c.*2050C>T, XM_017029835.2:c.*2050C>T, XM_017029835.1:c.*2050C>T, XM_011531194.2:c.*2050C>T, XM_011531194.1:c.*2050C>T, XM_011531195.2:c.*2050C>T, XM_011531195.1:c.*2050C>T, XM_047442488.1:c.*2050C>T, XM_047442489.1:c.*2050C>T, XM_047442490.1:c.*2050C>T, XM_047442491.1:c.*2050C>T, XM_047442496.1:c.*2050C>T, XM_047442492.1:c.*2050C>T, XM_047442493.1:c.*2050C>T, XM_047442494.1:c.*2050C>T, XM_047442495.1:c.*2050C>T, XM_047442497.1:c.*2050C>T, XM_047442498.1:c.*2050C>T, XM_047442499.1:c.*2050C>T, XM_047442500.1:c.*2050C>T, XM_047442501.1:c.*2050C>T, XM_047442502.1:c.*2050C>T, XM_047442503.1:c.*2050C>T, XM_047442505.1:c.*2050C>T, XM_047442507.1:c.*2050C>T, XM_047442508.1:c.*2050C>T, XM_047442509.1:c.*2050C>T, NM_001178114.1:c.*2050C>T, XM_047442506.1:c.*2050C>T, XM_047442504.1:c.*2050C>T

      3.

      rs1486876249 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        X:152972275 (GRCh38)
        X:152140819 (GRCh37)
        Canonical SPDI:
        NC_000023.11:152972274:C:T
        Gene:
        ZNF185 (Varview)
        Functional Consequence:
        3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0./0 (ALFA)
        T=0.000008/2 (TOPMED)
        T=0.00001/1 (GnomAD)
        HGVS:
        NC_000023.11:g.152972275C>T, NW_003871103.3:g.406258C>T, NG_021255.2:g.62834C>T, NM_007150.3:c.*1002C>T, NM_001178108.2:c.*1002C>T, NM_001178108.1:c.*1002C>T, NM_001388432.2:c.*1002C>T, NM_001388432.1:c.*1002C>T, NM_001178113.2:c.*1002C>T, NM_001178113.1:c.*1002C>T, NM_001178115.2:c.*1002C>T, NM_001178115.1:c.*1002C>T, NM_001178106.1:c.*1002C>T, NM_001395254.1:c.*1002C>T, NM_001178107.1:c.*1002C>T, NM_001178109.1:c.*1002C>T, NM_001178110.1:c.*1002C>T, NW_025791818.1:g.587465C>T, NC_000023.10:g.152140819C>T, XM_005274746.4:c.*1002C>T, XM_005274746.3:c.*1002C>T, XM_005274746.2:c.*1002C>T, XM_005274746.1:c.*1002C>T, XM_017029822.3:c.*1002C>T, XM_017029822.2:c.*1002C>T, XM_017029822.1:c.*1002C>T, XM_005274738.3:c.*1002C>T, XM_005274738.2:c.*1002C>T, XM_005274738.1:c.*1002C>T, XM_005274741.3:c.*1002C>T, XM_005274741.2:c.*1002C>T, XM_005274741.1:c.*1002C>T, XM_005274740.3:c.*1002C>T, XM_005274740.2:c.*1002C>T, XM_005274740.1:c.*1002C>T, XM_005274742.3:c.*1002C>T, XM_005274742.2:c.*1002C>T, XM_005274742.1:c.*1002C>T, XM_005274744.3:c.*1002C>T, XM_005274744.2:c.*1002C>T, XM_005274744.1:c.*1002C>T, XM_005274745.3:c.*1002C>T, XM_005274745.2:c.*1002C>T, XM_005274745.1:c.*1002C>T, XM_017029821.2:c.*1002C>T, XM_017029821.1:c.*1002C>T, XM_017029823.2:c.*1002C>T, XM_017029823.1:c.*1002C>T, XM_017029824.2:c.*1002C>T, XM_017029824.1:c.*1002C>T, XM_017029825.2:c.*1002C>T, XM_017029825.1:c.*1002C>T, XM_017029826.2:c.*1002C>T, XM_017029826.1:c.*1002C>T, XM_017029827.2:c.*1002C>T, XM_017029827.1:c.*1002C>T, XM_017029828.2:c.*1002C>T, XM_017029828.1:c.*1002C>T, XM_017029829.2:c.*1002C>T, XM_017029829.1:c.*1002C>T, XM_017029830.2:c.*1002C>T, XM_017029830.1:c.*1002C>T, XM_017029831.2:c.*1002C>T, XM_017029831.1:c.*1002C>T, XM_017029832.2:c.*1002C>T, XM_017029832.1:c.*1002C>T, XM_017029833.2:c.*1002C>T, XM_017029833.1:c.*1002C>T, XM_017029834.2:c.*1002C>T, XM_017029834.1:c.*1002C>T, XM_017029835.2:c.*1002C>T, XM_017029835.1:c.*1002C>T, XM_011531194.2:c.*1002C>T, XM_011531194.1:c.*1002C>T, XM_011531195.2:c.*1002C>T, XM_011531195.1:c.*1002C>T, XM_047442488.1:c.*1002C>T, XM_047442489.1:c.*1002C>T, XM_047442490.1:c.*1002C>T, XM_047442491.1:c.*1002C>T, XM_047442496.1:c.*1002C>T, XM_047442492.1:c.*1002C>T, XM_047442493.1:c.*1002C>T, XM_047442494.1:c.*1002C>T, XM_047442495.1:c.*1002C>T, XM_047442497.1:c.*1002C>T, XM_047442498.1:c.*1002C>T, XM_047442499.1:c.*1002C>T, XM_047442500.1:c.*1002C>T, XM_047442501.1:c.*1002C>T, XM_047442502.1:c.*1002C>T, XM_047442503.1:c.*1002C>T, XM_047442505.1:c.*1002C>T, XM_047442507.1:c.*1002C>T, XM_047442508.1:c.*1002C>T, XM_047442509.1:c.*1002C>T, NM_001178114.1:c.*1002C>T, XM_047442506.1:c.*1002C>T, XM_047442504.1:c.*1002C>T

        4.

        rs1486830627 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AGTT>- [Show Flanks]
          Chromosome:
          X:152971793 (GRCh38)
          X:152140337 (GRCh37)
          Canonical SPDI:
          NC_000023.11:152971787:TAGTTAGTT:TAGTT
          Gene:
          ZNF185 (Varview)
          Functional Consequence:
          3_prime_UTR_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TAGTT=0./0 (ALFA)
          -=0.000038/4 (GnomAD)
          -=0.000049/13 (TOPMED)
          HGVS:
          NC_000023.11:g.152971789AGTT[1], NW_003871103.3:g.405772AGTT[1], NG_021255.2:g.62348AGTT[1], NM_007150.3:c.*516AGTT[1], NM_001178108.2:c.*516AGTT[1], NM_001178108.1:c.*516AGTT[1], NM_001388432.2:c.*516AGTT[1], NM_001388432.1:c.*516AGTT[1], NM_001178113.2:c.*516AGTT[1], NM_001178113.1:c.*516AGTT[1], NM_001178115.2:c.*516AGTT[1], NM_001178115.1:c.*516AGTT[1], NM_001178106.1:c.*516AGTT[1], NM_001395254.1:c.*516AGTT[1], NM_001178107.1:c.*516AGTT[1], NM_001178109.1:c.*516AGTT[1], NM_001178110.1:c.*516AGTT[1], NW_025791818.1:g.586979AGTT[1], NC_000023.10:g.152140333AGTT[1], XM_005274746.4:c.*516AGTT[1], XM_005274746.3:c.*516AGTT[1], XM_005274746.2:c.*516AGTT[1], XM_005274746.1:c.*516AGTT[1], XM_017029822.3:c.*516AGTT[1], XM_017029822.2:c.*516AGTT[1], XM_017029822.1:c.*516AGTT[1], XM_005274738.3:c.*516AGTT[1], XM_005274738.2:c.*516AGTT[1], XM_005274738.1:c.*516AGTT[1], XM_005274741.3:c.*516AGTT[1], XM_005274741.2:c.*516AGTT[1], XM_005274741.1:c.*516AGTT[1], XM_005274740.3:c.*516AGTT[1], XM_005274740.2:c.*516AGTT[1], XM_005274740.1:c.*516AGTT[1], XM_005274742.3:c.*516AGTT[1], XM_005274742.2:c.*516AGTT[1], XM_005274742.1:c.*516AGTT[1], XM_005274744.3:c.*516AGTT[1], XM_005274744.2:c.*516AGTT[1], XM_005274744.1:c.*516AGTT[1], XM_005274745.3:c.*516AGTT[1], XM_005274745.2:c.*516AGTT[1], XM_005274745.1:c.*516AGTT[1], XM_017029821.2:c.*516AGTT[1], XM_017029821.1:c.*516AGTT[1], XM_017029823.2:c.*516AGTT[1], XM_017029823.1:c.*516AGTT[1], XM_017029824.2:c.*516AGTT[1], XM_017029824.1:c.*516AGTT[1], XM_017029825.2:c.*516AGTT[1], XM_017029825.1:c.*516AGTT[1], XM_017029826.2:c.*516AGTT[1], XM_017029826.1:c.*516AGTT[1], XM_017029827.2:c.*516AGTT[1], XM_017029827.1:c.*516AGTT[1], XM_017029828.2:c.*516AGTT[1], XM_017029828.1:c.*516AGTT[1], XM_017029829.2:c.*516AGTT[1], XM_017029829.1:c.*516AGTT[1], XM_017029830.2:c.*516AGTT[1], XM_017029830.1:c.*516AGTT[1], XM_017029831.2:c.*516AGTT[1], XM_017029831.1:c.*516AGTT[1], XM_017029832.2:c.*516AGTT[1], XM_017029832.1:c.*516AGTT[1], XM_017029833.2:c.*516AGTT[1], XM_017029833.1:c.*516AGTT[1], XM_017029834.2:c.*516AGTT[1], XM_017029834.1:c.*516AGTT[1], XM_017029835.2:c.*516AGTT[1], XM_017029835.1:c.*516AGTT[1], XM_011531194.2:c.*516AGTT[1], XM_011531194.1:c.*516AGTT[1], XM_011531195.2:c.*516AGTT[1], XM_011531195.1:c.*516AGTT[1], XM_047442488.1:c.*516AGTT[1], XM_047442489.1:c.*516AGTT[1], XM_047442490.1:c.*516AGTT[1], XM_047442491.1:c.*516AGTT[1], XM_047442496.1:c.*516AGTT[1], XM_047442492.1:c.*516AGTT[1], XM_047442493.1:c.*516AGTT[1], XM_047442494.1:c.*516AGTT[1], XM_047442495.1:c.*516AGTT[1], XM_047442497.1:c.*516AGTT[1], XM_047442498.1:c.*516AGTT[1], XM_047442499.1:c.*516AGTT[1], XM_047442500.1:c.*516AGTT[1], XM_047442501.1:c.*516AGTT[1], XM_047442502.1:c.*516AGTT[1], XM_047442503.1:c.*516AGTT[1], XM_047442505.1:c.*516AGTT[1], XM_047442507.1:c.*516AGTT[1], XM_047442508.1:c.*516AGTT[1], XM_047442509.1:c.*516AGTT[1], NM_001178114.1:c.*516AGTT[1], XM_047442506.1:c.*516AGTT[1], XM_047442504.1:c.*516AGTT[1]

          5.

          rs1486799312 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            X:152973152 (GRCh38)
            X:152141696 (GRCh37)
            Canonical SPDI:
            NC_000023.11:152973151:C:T
            Gene:
            ZNF185 (Varview)
            Functional Consequence:
            3_prime_UTR_variant
            Validated:
            by frequency,by alfa
            MAF:
            T=0./0 (ALFA)
            HGVS:
            NC_000023.11:g.152973152C>T, NW_003871103.3:g.407135C>T, NG_021255.2:g.63711C>T, NM_007150.3:c.*1879C>T, NM_001178108.2:c.*1879C>T, NM_001178108.1:c.*1879C>T, NM_001388432.2:c.*1879C>T, NM_001388432.1:c.*1879C>T, NM_001178113.2:c.*1879C>T, NM_001178113.1:c.*1879C>T, NM_001178115.2:c.*1879C>T, NM_001178115.1:c.*1879C>T, NM_001178106.1:c.*1879C>T, NM_001395254.1:c.*1879C>T, NM_001178107.1:c.*1879C>T, NM_001178109.1:c.*1879C>T, NM_001178110.1:c.*1879C>T, NW_025791818.1:g.588342C>T, NC_000023.10:g.152141696C>T, XM_005274746.4:c.*1879C>T, XM_005274746.3:c.*1879C>T, XM_005274746.2:c.*1879C>T, XM_005274746.1:c.*1879C>T, XM_017029822.3:c.*1879C>T, XM_017029822.2:c.*1879C>T, XM_017029822.1:c.*1879C>T, XM_005274738.3:c.*1879C>T, XM_005274738.2:c.*1879C>T, XM_005274738.1:c.*1879C>T, XM_005274741.3:c.*1879C>T, XM_005274741.2:c.*1879C>T, XM_005274741.1:c.*1879C>T, XM_005274740.3:c.*1879C>T, XM_005274740.2:c.*1879C>T, XM_005274740.1:c.*1879C>T, XM_005274742.3:c.*1879C>T, XM_005274742.2:c.*1879C>T, XM_005274742.1:c.*1879C>T, XM_005274744.3:c.*1879C>T, XM_005274744.2:c.*1879C>T, XM_005274744.1:c.*1879C>T, XM_005274745.3:c.*1879C>T, XM_005274745.2:c.*1879C>T, XM_005274745.1:c.*1879C>T, XM_017029821.2:c.*1879C>T, XM_017029821.1:c.*1879C>T, XM_017029823.2:c.*1879C>T, XM_017029823.1:c.*1879C>T, XM_017029824.2:c.*1879C>T, XM_017029824.1:c.*1879C>T, XM_017029825.2:c.*1879C>T, XM_017029825.1:c.*1879C>T, XM_017029826.2:c.*1879C>T, XM_017029826.1:c.*1879C>T, XM_017029827.2:c.*1879C>T, XM_017029827.1:c.*1879C>T, XM_017029828.2:c.*1879C>T, XM_017029828.1:c.*1879C>T, XM_017029829.2:c.*1879C>T, XM_017029829.1:c.*1879C>T, XM_017029830.2:c.*1879C>T, XM_017029830.1:c.*1879C>T, XM_017029831.2:c.*1879C>T, XM_017029831.1:c.*1879C>T, XM_017029832.2:c.*1879C>T, XM_017029832.1:c.*1879C>T, XM_017029833.2:c.*1879C>T, XM_017029833.1:c.*1879C>T, XM_017029834.2:c.*1879C>T, XM_017029834.1:c.*1879C>T, XM_017029835.2:c.*1879C>T, XM_017029835.1:c.*1879C>T, XM_011531194.2:c.*1879C>T, XM_011531194.1:c.*1879C>T, XM_011531195.2:c.*1879C>T, XM_011531195.1:c.*1879C>T, XM_047442488.1:c.*1879C>T, XM_047442489.1:c.*1879C>T, XM_047442490.1:c.*1879C>T, XM_047442491.1:c.*1879C>T, XM_047442496.1:c.*1879C>T, XM_047442492.1:c.*1879C>T, XM_047442493.1:c.*1879C>T, XM_047442494.1:c.*1879C>T, XM_047442495.1:c.*1879C>T, XM_047442497.1:c.*1879C>T, XM_047442498.1:c.*1879C>T, XM_047442499.1:c.*1879C>T, XM_047442500.1:c.*1879C>T, XM_047442501.1:c.*1879C>T, XM_047442502.1:c.*1879C>T, XM_047442503.1:c.*1879C>T, XM_047442505.1:c.*1879C>T, XM_047442507.1:c.*1879C>T, XM_047442508.1:c.*1879C>T, XM_047442509.1:c.*1879C>T, NM_001178114.1:c.*1879C>T, XM_047442506.1:c.*1879C>T, XM_047442504.1:c.*1879C>T

            6.

            rs1485985223 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G,T [Show Flanks]
              Chromosome:
              X:152973004 (GRCh38)
              X:152141548 (GRCh37)
              Canonical SPDI:
              NC_000023.11:152973003:C:G,NC_000023.11:152973003:C:T
              Gene:
              ZNF185 (Varview)
              Functional Consequence:
              3_prime_UTR_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0./0 (ALFA)
              T=0.000004/1 (TOPMED)
              HGVS:
              NC_000023.11:g.152973004C>G, NC_000023.11:g.152973004C>T, NW_003871103.3:g.406987C>G, NW_003871103.3:g.406987C>T, NG_021255.2:g.63563C>G, NG_021255.2:g.63563C>T, NM_007150.3:c.*1731C>G, NM_007150.3:c.*1731C>T, NM_001178108.2:c.*1731C>G, NM_001178108.2:c.*1731C>T, NM_001178108.1:c.*1731C>G, NM_001178108.1:c.*1731C>T, NM_001388432.2:c.*1731C>G, NM_001388432.2:c.*1731C>T, NM_001388432.1:c.*1731C>G, NM_001388432.1:c.*1731C>T, NM_001178113.2:c.*1731C>G, NM_001178113.2:c.*1731C>T, NM_001178113.1:c.*1731C>G, NM_001178113.1:c.*1731C>T, NM_001178115.2:c.*1731C>G, NM_001178115.2:c.*1731C>T, NM_001178115.1:c.*1731C>G, NM_001178115.1:c.*1731C>T, NM_001178106.1:c.*1731C>G, NM_001178106.1:c.*1731C>T, NM_001395254.1:c.*1731C>G, NM_001395254.1:c.*1731C>T, NM_001178107.1:c.*1731C>G, NM_001178107.1:c.*1731C>T, NM_001178109.1:c.*1731C>G, NM_001178109.1:c.*1731C>T, NM_001178110.1:c.*1731C>G, NM_001178110.1:c.*1731C>T, NW_025791818.1:g.588194C>G, NW_025791818.1:g.588194C>T, NC_000023.10:g.152141548C>G, NC_000023.10:g.152141548C>T, XM_005274746.4:c.*1731C>G, XM_005274746.4:c.*1731C>T, XM_005274746.3:c.*1731C>G, XM_005274746.3:c.*1731C>T, XM_005274746.2:c.*1731C>G, XM_005274746.2:c.*1731C>T, XM_005274746.1:c.*1731C>G, XM_005274746.1:c.*1731C>T, XM_017029822.3:c.*1731C>G, XM_017029822.3:c.*1731C>T, XM_017029822.2:c.*1731C>G, XM_017029822.2:c.*1731C>T, XM_017029822.1:c.*1731C>G, XM_017029822.1:c.*1731C>T, XM_005274738.3:c.*1731C>G, XM_005274738.3:c.*1731C>T, XM_005274738.2:c.*1731C>G, XM_005274738.2:c.*1731C>T, XM_005274738.1:c.*1731C>G, XM_005274738.1:c.*1731C>T, XM_005274741.3:c.*1731C>G, XM_005274741.3:c.*1731C>T, XM_005274741.2:c.*1731C>G, XM_005274741.2:c.*1731C>T, XM_005274741.1:c.*1731C>G, XM_005274741.1:c.*1731C>T, XM_005274740.3:c.*1731C>G, XM_005274740.3:c.*1731C>T, XM_005274740.2:c.*1731C>G, XM_005274740.2:c.*1731C>T, XM_005274740.1:c.*1731C>G, XM_005274740.1:c.*1731C>T, XM_005274742.3:c.*1731C>G, XM_005274742.3:c.*1731C>T, XM_005274742.2:c.*1731C>G, XM_005274742.2:c.*1731C>T, XM_005274742.1:c.*1731C>G, XM_005274742.1:c.*1731C>T, XM_005274744.3:c.*1731C>G, XM_005274744.3:c.*1731C>T, XM_005274744.2:c.*1731C>G, XM_005274744.2:c.*1731C>T, XM_005274744.1:c.*1731C>G, XM_005274744.1:c.*1731C>T, XM_005274745.3:c.*1731C>G, XM_005274745.3:c.*1731C>T, XM_005274745.2:c.*1731C>G, XM_005274745.2:c.*1731C>T, XM_005274745.1:c.*1731C>G, XM_005274745.1:c.*1731C>T, XM_017029821.2:c.*1731C>G, XM_017029821.2:c.*1731C>T, XM_017029821.1:c.*1731C>G, XM_017029821.1:c.*1731C>T, XM_017029823.2:c.*1731C>G, XM_017029823.2:c.*1731C>T, XM_017029823.1:c.*1731C>G, XM_017029823.1:c.*1731C>T, XM_017029824.2:c.*1731C>G, XM_017029824.2:c.*1731C>T, XM_017029824.1:c.*1731C>G, XM_017029824.1:c.*1731C>T, XM_017029825.2:c.*1731C>G, XM_017029825.2:c.*1731C>T, XM_017029825.1:c.*1731C>G, XM_017029825.1:c.*1731C>T, XM_017029826.2:c.*1731C>G, XM_017029826.2:c.*1731C>T, XM_017029826.1:c.*1731C>G, XM_017029826.1:c.*1731C>T, XM_017029827.2:c.*1731C>G, XM_017029827.2:c.*1731C>T, XM_017029827.1:c.*1731C>G, XM_017029827.1:c.*1731C>T, XM_017029828.2:c.*1731C>G, XM_017029828.2:c.*1731C>T, XM_017029828.1:c.*1731C>G, XM_017029828.1:c.*1731C>T, XM_017029829.2:c.*1731C>G, XM_017029829.2:c.*1731C>T, XM_017029829.1:c.*1731C>G, XM_017029829.1:c.*1731C>T, XM_017029830.2:c.*1731C>G, XM_017029830.2:c.*1731C>T, XM_017029830.1:c.*1731C>G, XM_017029830.1:c.*1731C>T, XM_017029831.2:c.*1731C>G, XM_017029831.2:c.*1731C>T, XM_017029831.1:c.*1731C>G, XM_017029831.1:c.*1731C>T, XM_017029832.2:c.*1731C>G, XM_017029832.2:c.*1731C>T, XM_017029832.1:c.*1731C>G, XM_017029832.1:c.*1731C>T, XM_017029833.2:c.*1731C>G, XM_017029833.2:c.*1731C>T, XM_017029833.1:c.*1731C>G, XM_017029833.1:c.*1731C>T, XM_017029834.2:c.*1731C>G, XM_017029834.2:c.*1731C>T, XM_017029834.1:c.*1731C>G, XM_017029834.1:c.*1731C>T, XM_017029835.2:c.*1731C>G, XM_017029835.2:c.*1731C>T, XM_017029835.1:c.*1731C>G, XM_017029835.1:c.*1731C>T, XM_011531194.2:c.*1731C>G, XM_011531194.2:c.*1731C>T, XM_011531194.1:c.*1731C>G, XM_011531194.1:c.*1731C>T, XM_011531195.2:c.*1731C>G, XM_011531195.2:c.*1731C>T, XM_011531195.1:c.*1731C>G, XM_011531195.1:c.*1731C>T, XM_047442488.1:c.*1731C>G, XM_047442488.1:c.*1731C>T, XM_047442489.1:c.*1731C>G, XM_047442489.1:c.*1731C>T, XM_047442490.1:c.*1731C>G, XM_047442490.1:c.*1731C>T, XM_047442491.1:c.*1731C>G, XM_047442491.1:c.*1731C>T, XM_047442496.1:c.*1731C>G, XM_047442496.1:c.*1731C>T, XM_047442492.1:c.*1731C>G, XM_047442492.1:c.*1731C>T, XM_047442493.1:c.*1731C>G, XM_047442493.1:c.*1731C>T, XM_047442494.1:c.*1731C>G, XM_047442494.1:c.*1731C>T, XM_047442495.1:c.*1731C>G, XM_047442495.1:c.*1731C>T, XM_047442497.1:c.*1731C>G, XM_047442497.1:c.*1731C>T, XM_047442498.1:c.*1731C>G, XM_047442498.1:c.*1731C>T, XM_047442499.1:c.*1731C>G, XM_047442499.1:c.*1731C>T, XM_047442500.1:c.*1731C>G, XM_047442500.1:c.*1731C>T, XM_047442501.1:c.*1731C>G, XM_047442501.1:c.*1731C>T, XM_047442502.1:c.*1731C>G, XM_047442502.1:c.*1731C>T, XM_047442503.1:c.*1731C>G, XM_047442503.1:c.*1731C>T, XM_047442505.1:c.*1731C>G, XM_047442505.1:c.*1731C>T, XM_047442507.1:c.*1731C>G, XM_047442507.1:c.*1731C>T, XM_047442508.1:c.*1731C>G, XM_047442508.1:c.*1731C>T, XM_047442509.1:c.*1731C>G, XM_047442509.1:c.*1731C>T, NM_001178114.1:c.*1731C>G, NM_001178114.1:c.*1731C>T, XM_047442506.1:c.*1731C>G, XM_047442506.1:c.*1731C>T, XM_047442504.1:c.*1731C>G, XM_047442504.1:c.*1731C>T

              7.

              rs1485892406 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>T [Show Flanks]
                Chromosome:
                X:152971654 (GRCh38)
                X:152140198 (GRCh37)
                Canonical SPDI:
                NC_000023.11:152971653:G:T
                Gene:
                ZNF185 (Varview)
                Functional Consequence:
                3_prime_UTR_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                T=0.00001/1 (GnomAD)
                T=0.000011/3 (TOPMED)
                HGVS:
                NC_000023.11:g.152971654G>T, NW_003871103.3:g.405637G>T, NG_021255.2:g.62213G>T, NM_007150.3:c.*381G>T, NM_001178108.2:c.*381G>T, NM_001178108.1:c.*381G>T, NM_001388432.2:c.*381G>T, NM_001388432.1:c.*381G>T, NM_001178113.2:c.*381G>T, NM_001178113.1:c.*381G>T, NM_001178115.2:c.*381G>T, NM_001178115.1:c.*381G>T, NM_001178106.1:c.*381G>T, NM_001395254.1:c.*381G>T, NM_001178107.1:c.*381G>T, NM_001178109.1:c.*381G>T, NM_001178110.1:c.*381G>T, NW_025791818.1:g.586844G>T, NC_000023.10:g.152140198G>T, XM_005274746.4:c.*381G>T, XM_005274746.3:c.*381G>T, XM_005274746.2:c.*381G>T, XM_005274746.1:c.*381G>T, XM_017029822.3:c.*381G>T, XM_017029822.2:c.*381G>T, XM_017029822.1:c.*381G>T, XM_005274738.3:c.*381G>T, XM_005274738.2:c.*381G>T, XM_005274738.1:c.*381G>T, XM_005274741.3:c.*381G>T, XM_005274741.2:c.*381G>T, XM_005274741.1:c.*381G>T, XM_005274740.3:c.*381G>T, XM_005274740.2:c.*381G>T, XM_005274740.1:c.*381G>T, XM_005274742.3:c.*381G>T, XM_005274742.2:c.*381G>T, XM_005274742.1:c.*381G>T, XM_005274744.3:c.*381G>T, XM_005274744.2:c.*381G>T, XM_005274744.1:c.*381G>T, XM_005274745.3:c.*381G>T, XM_005274745.2:c.*381G>T, XM_005274745.1:c.*381G>T, XM_017029821.2:c.*381G>T, XM_017029821.1:c.*381G>T, XM_017029823.2:c.*381G>T, XM_017029823.1:c.*381G>T, XM_017029824.2:c.*381G>T, XM_017029824.1:c.*381G>T, XM_017029825.2:c.*381G>T, XM_017029825.1:c.*381G>T, XM_017029826.2:c.*381G>T, XM_017029826.1:c.*381G>T, XM_017029827.2:c.*381G>T, XM_017029827.1:c.*381G>T, XM_017029828.2:c.*381G>T, XM_017029828.1:c.*381G>T, XM_017029829.2:c.*381G>T, XM_017029829.1:c.*381G>T, XM_017029830.2:c.*381G>T, XM_017029830.1:c.*381G>T, XM_017029831.2:c.*381G>T, XM_017029831.1:c.*381G>T, XM_017029832.2:c.*381G>T, XM_017029832.1:c.*381G>T, XM_017029833.2:c.*381G>T, XM_017029833.1:c.*381G>T, XM_017029834.2:c.*381G>T, XM_017029834.1:c.*381G>T, XM_017029835.2:c.*381G>T, XM_017029835.1:c.*381G>T, XM_011531194.2:c.*381G>T, XM_011531194.1:c.*381G>T, XM_011531195.2:c.*381G>T, XM_011531195.1:c.*381G>T, XM_047442488.1:c.*381G>T, XM_047442489.1:c.*381G>T, XM_047442490.1:c.*381G>T, XM_047442491.1:c.*381G>T, XM_047442496.1:c.*381G>T, XM_047442492.1:c.*381G>T, XM_047442493.1:c.*381G>T, XM_047442494.1:c.*381G>T, XM_047442495.1:c.*381G>T, XM_047442497.1:c.*381G>T, XM_047442498.1:c.*381G>T, XM_047442499.1:c.*381G>T, XM_047442500.1:c.*381G>T, XM_047442501.1:c.*381G>T, XM_047442502.1:c.*381G>T, XM_047442503.1:c.*381G>T, XM_047442505.1:c.*381G>T, XM_047442507.1:c.*381G>T, XM_047442508.1:c.*381G>T, XM_047442509.1:c.*381G>T, NM_001178114.1:c.*381G>T, XM_047442506.1:c.*381G>T, XM_047442504.1:c.*381G>T

                8.

                rs1484067793 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>T [Show Flanks]
                  Chromosome:
                  X:152963947 (GRCh38)
                  X:152132491 (GRCh37)
                  Canonical SPDI:
                  NC_000023.11:152963946:C:T
                  Gene:
                  ZNF185 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,synonymous_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0.000071/1 (ALFA)
                  T=0.00001/1 (GnomAD)
                  HGVS:
                  NC_000023.11:g.152963947C>T, NW_003871103.3:g.397930C>T, NG_021255.2:g.54506C>T, NM_007150.3:c.1713C>T, NM_001178108.2:c.1716C>T, NM_001178108.1:c.1716C>T, NM_001388432.2:c.1716C>T, NM_001388432.1:c.1716C>T, NM_001178113.2:c.1050C>T, NM_001178113.1:c.1050C>T, NM_001178115.2:c.627C>T, NM_001178115.1:c.627C>T, NM_001178106.1:c.1809C>T, NM_001395254.1:c.1812C>T, NM_001178107.1:c.1722C>T, NM_001178109.1:c.1626C>T, NM_001178110.1:c.1536C>T, NW_025791818.1:g.579137C>T, NC_000023.10:g.152132491C>T, XM_005274746.4:c.1455C>T, XM_005274746.3:c.1455C>T, XM_005274746.2:c.1455C>T, XM_005274746.1:c.1455C>T, XM_017029822.3:c.1944C>T, XM_017029822.2:c.1944C>T, XM_017029822.1:c.1944C>T, XM_005274738.3:c.1713C>T, XM_005274738.2:c.1713C>T, XM_005274738.1:c.1713C>T, XM_005274741.3:c.1626C>T, XM_005274741.2:c.1626C>T, XM_005274741.1:c.1626C>T, XM_005274740.3:c.1626C>T, XM_005274740.2:c.1626C>T, XM_005274740.1:c.1626C>T, XM_005274742.3:c.1623C>T, XM_005274742.2:c.1623C>T, XM_005274742.1:c.1623C>T, XM_005274744.3:c.1539C>T, XM_005274744.2:c.1539C>T, XM_005274744.1:c.1539C>T, XM_005274745.3:c.1536C>T, XM_005274745.2:c.1536C>T, XM_005274745.1:c.1536C>T, XM_017029821.2:c.1944C>T, XM_017029821.1:c.1944C>T, XM_017029823.2:c.1941C>T, XM_017029823.1:c.1941C>T, XM_017029824.2:c.1860C>T, XM_017029824.1:c.1860C>T, XM_017029825.2:c.1857C>T, XM_017029825.1:c.1857C>T, XM_017029826.2:c.1854C>T, XM_017029826.1:c.1854C>T, XM_017029827.2:c.1851C>T, XM_017029827.1:c.1851C>T, XM_017029828.2:c.1848C>T, XM_017029828.1:c.1848C>T, XM_017029829.2:c.1767C>T, XM_017029829.1:c.1767C>T, XM_017029830.2:c.1761C>T, XM_017029830.1:c.1761C>T, XM_017029831.2:c.1758C>T, XM_017029831.1:c.1758C>T, XM_017029832.2:c.1749C>T, XM_017029832.1:c.1749C>T, XM_017029833.2:c.1683C>T, XM_017029833.1:c.1683C>T, XM_017029834.2:c.1671C>T, XM_017029834.1:c.1671C>T, XM_017029835.2:c.1632C>T, XM_017029835.1:c.1632C>T, XM_011531194.2:c.1617C>T, XM_011531194.1:c.1617C>T, XM_011531195.2:c.1614C>T, XM_011531195.1:c.1614C>T, XM_047442488.1:c.1845C>T, XM_047442489.1:c.1755C>T, XM_047442490.1:c.1725C>T, XM_047442491.1:c.1722C>T, XM_047442496.1:c.1626C>T, XM_047442492.1:c.1638C>T, XM_047442493.1:c.1635C>T, XM_047442494.1:c.1632C>T, XM_047442495.1:c.1629C>T, XM_047442497.1:c.1614C>T, XM_047442498.1:c.1545C>T, XM_047442499.1:c.1542C>T, XM_047442500.1:c.1530C>T, XM_047442501.1:c.1518C>T, XM_047442502.1:c.1515C>T, XM_047442503.1:c.1440C>T, XM_047442505.1:c.1437C>T, XM_047442507.1:c.1428C>T, XM_047442508.1:c.1356C>T, XM_047442509.1:c.1341C>T, NM_001178114.1:c.1002C>T, XM_047442506.1:c.1431C>T, XM_047442504.1:c.1437C>T

                  9.

                  rs1483605766 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAT>- [Show Flanks]
                    Chromosome:
                    X:152973457 (GRCh38)
                    X:152142001 (GRCh37)
                    Canonical SPDI:
                    NC_000023.11:152973453:AATAAAT:AAT
                    Gene:
                    ZNF185 (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAT=0./0 (ALFA)
                    -=0.000034/9 (TOPMED)
                    -=0.000095/10 (GnomAD)
                    HGVS:
                    NC_000023.11:g.152973457_152973460del, NW_003871103.3:g.407440_407443del, NG_021255.2:g.64016_64019del, NM_007150.3:c.*2184_*2187del, NM_001178108.2:c.*2184_*2187del, NM_001178108.1:c.*2184_*2187del, NM_001388432.2:c.*2184_*2187del, NM_001388432.1:c.*2184_*2187del, NM_001178113.2:c.*2184_*2187del, NM_001178113.1:c.*2184_*2187del, NM_001178115.2:c.*2184_*2187del, NM_001178115.1:c.*2184_*2187del, NM_001178106.1:c.*2184_*2187del, NM_001395254.1:c.*2184_*2187del, NM_001178107.1:c.*2184_*2187del, NM_001178109.1:c.*2184_*2187del, NM_001178110.1:c.*2184_*2187del, NW_025791818.1:g.588647_588650del, NC_000023.10:g.152142001_152142004del, XM_005274746.4:c.*2184_*2187del, XM_005274746.3:c.*2184_*2187del, XM_005274746.2:c.*2184_*2187del, XM_005274746.1:c.*2184_*2187del, XM_017029822.3:c.*2184_*2187del, XM_017029822.2:c.*2184_*2187del, XM_017029822.1:c.*2184_*2187del, XM_005274738.3:c.*2184_*2187del, XM_005274738.2:c.*2184_*2187del, XM_005274738.1:c.*2184_*2187del, XM_005274741.3:c.*2184_*2187del, XM_005274741.2:c.*2184_*2187del, XM_005274741.1:c.*2184_*2187del, XM_005274740.3:c.*2184_*2187del, XM_005274740.2:c.*2184_*2187del, XM_005274740.1:c.*2184_*2187del, XM_005274742.3:c.*2184_*2187del, XM_005274742.2:c.*2184_*2187del, XM_005274742.1:c.*2184_*2187del, XM_005274744.3:c.*2184_*2187del, XM_005274744.2:c.*2184_*2187del, XM_005274744.1:c.*2184_*2187del, XM_005274745.3:c.*2184_*2187del, XM_005274745.2:c.*2184_*2187del, XM_005274745.1:c.*2184_*2187del, XM_017029821.2:c.*2184_*2187del, XM_017029821.1:c.*2184_*2187del, XM_017029823.2:c.*2184_*2187del, XM_017029823.1:c.*2184_*2187del, XM_017029824.2:c.*2184_*2187del, XM_017029824.1:c.*2184_*2187del, XM_017029825.2:c.*2184_*2187del, XM_017029825.1:c.*2184_*2187del, XM_017029826.2:c.*2184_*2187del, XM_017029826.1:c.*2184_*2187del, XM_017029827.2:c.*2184_*2187del, XM_017029827.1:c.*2184_*2187del, XM_017029828.2:c.*2184_*2187del, XM_017029828.1:c.*2184_*2187del, XM_017029829.2:c.*2184_*2187del, XM_017029829.1:c.*2184_*2187del, XM_017029830.2:c.*2184_*2187del, XM_017029830.1:c.*2184_*2187del, XM_017029831.2:c.*2184_*2187del, XM_017029831.1:c.*2184_*2187del, XM_017029832.2:c.*2184_*2187del, XM_017029832.1:c.*2184_*2187del, XM_017029833.2:c.*2184_*2187del, XM_017029833.1:c.*2184_*2187del, XM_017029834.2:c.*2184_*2187del, XM_017029834.1:c.*2184_*2187del, XM_017029835.2:c.*2184_*2187del, XM_017029835.1:c.*2184_*2187del, XM_011531194.2:c.*2184_*2187del, XM_011531194.1:c.*2184_*2187del, XM_011531195.2:c.*2184_*2187del, XM_011531195.1:c.*2184_*2187del, XM_047442488.1:c.*2184_*2187del, XM_047442489.1:c.*2184_*2187del, XM_047442490.1:c.*2184_*2187del, XM_047442491.1:c.*2184_*2187del, XM_047442496.1:c.*2184_*2187del, XM_047442492.1:c.*2184_*2187del, XM_047442493.1:c.*2184_*2187del, XM_047442494.1:c.*2184_*2187del, XM_047442495.1:c.*2184_*2187del, XM_047442497.1:c.*2184_*2187del, XM_047442498.1:c.*2184_*2187del, XM_047442499.1:c.*2184_*2187del, XM_047442500.1:c.*2184_*2187del, XM_047442501.1:c.*2184_*2187del, XM_047442502.1:c.*2184_*2187del, XM_047442503.1:c.*2184_*2187del, XM_047442505.1:c.*2184_*2187del, XM_047442507.1:c.*2184_*2187del, XM_047442508.1:c.*2184_*2187del, XM_047442509.1:c.*2184_*2187del, NM_001178114.1:c.*2184_*2187del, XM_047442506.1:c.*2184_*2187del, XM_047442504.1:c.*2184_*2187del

                    10.

                    rs1482626582 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>T [Show Flanks]
                      Chromosome:
                      X:152972822 (GRCh38)
                      X:152141366 (GRCh37)
                      Canonical SPDI:
                      NC_000023.11:152972821:C:T
                      Gene:
                      ZNF185 (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      T=0.000008/2 (TOPMED)
                      T=0.00001/1 (GnomAD)
                      HGVS:
                      NC_000023.11:g.152972822C>T, NW_003871103.3:g.406805C>T, NG_021255.2:g.63381C>T, NM_007150.3:c.*1549C>T, NM_001178108.2:c.*1549C>T, NM_001178108.1:c.*1549C>T, NM_001388432.2:c.*1549C>T, NM_001388432.1:c.*1549C>T, NM_001178113.2:c.*1549C>T, NM_001178113.1:c.*1549C>T, NM_001178115.2:c.*1549C>T, NM_001178115.1:c.*1549C>T, NM_001178106.1:c.*1549C>T, NM_001395254.1:c.*1549C>T, NM_001178107.1:c.*1549C>T, NM_001178109.1:c.*1549C>T, NM_001178110.1:c.*1549C>T, NW_025791818.1:g.588012C>T, NC_000023.10:g.152141366C>T, XM_005274746.4:c.*1549C>T, XM_005274746.3:c.*1549C>T, XM_005274746.2:c.*1549C>T, XM_005274746.1:c.*1549C>T, XM_017029822.3:c.*1549C>T, XM_017029822.2:c.*1549C>T, XM_017029822.1:c.*1549C>T, XM_005274738.3:c.*1549C>T, XM_005274738.2:c.*1549C>T, XM_005274738.1:c.*1549C>T, XM_005274741.3:c.*1549C>T, XM_005274741.2:c.*1549C>T, XM_005274741.1:c.*1549C>T, XM_005274740.3:c.*1549C>T, XM_005274740.2:c.*1549C>T, XM_005274740.1:c.*1549C>T, XM_005274742.3:c.*1549C>T, XM_005274742.2:c.*1549C>T, XM_005274742.1:c.*1549C>T, XM_005274744.3:c.*1549C>T, XM_005274744.2:c.*1549C>T, XM_005274744.1:c.*1549C>T, XM_005274745.3:c.*1549C>T, XM_005274745.2:c.*1549C>T, XM_005274745.1:c.*1549C>T, XM_017029821.2:c.*1549C>T, XM_017029821.1:c.*1549C>T, XM_017029823.2:c.*1549C>T, XM_017029823.1:c.*1549C>T, XM_017029824.2:c.*1549C>T, XM_017029824.1:c.*1549C>T, XM_017029825.2:c.*1549C>T, XM_017029825.1:c.*1549C>T, XM_017029826.2:c.*1549C>T, XM_017029826.1:c.*1549C>T, XM_017029827.2:c.*1549C>T, XM_017029827.1:c.*1549C>T, XM_017029828.2:c.*1549C>T, XM_017029828.1:c.*1549C>T, XM_017029829.2:c.*1549C>T, XM_017029829.1:c.*1549C>T, XM_017029830.2:c.*1549C>T, XM_017029830.1:c.*1549C>T, XM_017029831.2:c.*1549C>T, XM_017029831.1:c.*1549C>T, XM_017029832.2:c.*1549C>T, XM_017029832.1:c.*1549C>T, XM_017029833.2:c.*1549C>T, XM_017029833.1:c.*1549C>T, XM_017029834.2:c.*1549C>T, XM_017029834.1:c.*1549C>T, XM_017029835.2:c.*1549C>T, XM_017029835.1:c.*1549C>T, XM_011531194.2:c.*1549C>T, XM_011531194.1:c.*1549C>T, XM_011531195.2:c.*1549C>T, XM_011531195.1:c.*1549C>T, XM_047442488.1:c.*1549C>T, XM_047442489.1:c.*1549C>T, XM_047442490.1:c.*1549C>T, XM_047442491.1:c.*1549C>T, XM_047442496.1:c.*1549C>T, XM_047442492.1:c.*1549C>T, XM_047442493.1:c.*1549C>T, XM_047442494.1:c.*1549C>T, XM_047442495.1:c.*1549C>T, XM_047442497.1:c.*1549C>T, XM_047442498.1:c.*1549C>T, XM_047442499.1:c.*1549C>T, XM_047442500.1:c.*1549C>T, XM_047442501.1:c.*1549C>T, XM_047442502.1:c.*1549C>T, XM_047442503.1:c.*1549C>T, XM_047442505.1:c.*1549C>T, XM_047442507.1:c.*1549C>T, XM_047442508.1:c.*1549C>T, XM_047442509.1:c.*1549C>T, NM_001178114.1:c.*1549C>T, XM_047442506.1:c.*1549C>T, XM_047442504.1:c.*1549C>T

                      11.

                      rs1481074022 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C,G [Show Flanks]
                        Chromosome:
                        X:152972179 (GRCh38)
                        X:152140723 (GRCh37)
                        Canonical SPDI:
                        NC_000023.11:152972178:T:C,NC_000023.11:152972178:T:G
                        Gene:
                        ZNF185 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0./0 (ALFA)
                        G=0.00001/1 (GnomAD)
                        HGVS:
                        NC_000023.11:g.152972179T>C, NC_000023.11:g.152972179T>G, NW_003871103.3:g.406162T>C, NW_003871103.3:g.406162T>G, NG_021255.2:g.62738T>C, NG_021255.2:g.62738T>G, NM_007150.3:c.*906T>C, NM_007150.3:c.*906T>G, NM_001178108.2:c.*906T>C, NM_001178108.2:c.*906T>G, NM_001178108.1:c.*906T>C, NM_001178108.1:c.*906T>G, NM_001388432.2:c.*906T>C, NM_001388432.2:c.*906T>G, NM_001388432.1:c.*906T>C, NM_001388432.1:c.*906T>G, NM_001178113.2:c.*906T>C, NM_001178113.2:c.*906T>G, NM_001178113.1:c.*906T>C, NM_001178113.1:c.*906T>G, NM_001178115.2:c.*906T>C, NM_001178115.2:c.*906T>G, NM_001178115.1:c.*906T>C, NM_001178115.1:c.*906T>G, NM_001178106.1:c.*906T>C, NM_001178106.1:c.*906T>G, NM_001395254.1:c.*906T>C, NM_001395254.1:c.*906T>G, NM_001178107.1:c.*906T>C, NM_001178107.1:c.*906T>G, NM_001178109.1:c.*906T>C, NM_001178109.1:c.*906T>G, NM_001178110.1:c.*906T>C, NM_001178110.1:c.*906T>G, NW_025791818.1:g.587369T>C, NW_025791818.1:g.587369T>G, NC_000023.10:g.152140723T>C, NC_000023.10:g.152140723T>G, XM_005274746.4:c.*906T>C, XM_005274746.4:c.*906T>G, XM_005274746.3:c.*906T>C, XM_005274746.3:c.*906T>G, XM_005274746.2:c.*906T>C, XM_005274746.2:c.*906T>G, XM_005274746.1:c.*906T>C, XM_005274746.1:c.*906T>G, XM_017029822.3:c.*906T>C, XM_017029822.3:c.*906T>G, XM_017029822.2:c.*906T>C, XM_017029822.2:c.*906T>G, XM_017029822.1:c.*906T>C, XM_017029822.1:c.*906T>G, XM_005274738.3:c.*906T>C, XM_005274738.3:c.*906T>G, XM_005274738.2:c.*906T>C, XM_005274738.2:c.*906T>G, XM_005274738.1:c.*906T>C, XM_005274738.1:c.*906T>G, XM_005274741.3:c.*906T>C, XM_005274741.3:c.*906T>G, XM_005274741.2:c.*906T>C, XM_005274741.2:c.*906T>G, XM_005274741.1:c.*906T>C, XM_005274741.1:c.*906T>G, XM_005274740.3:c.*906T>C, XM_005274740.3:c.*906T>G, XM_005274740.2:c.*906T>C, XM_005274740.2:c.*906T>G, XM_005274740.1:c.*906T>C, XM_005274740.1:c.*906T>G, XM_005274742.3:c.*906T>C, XM_005274742.3:c.*906T>G, XM_005274742.2:c.*906T>C, XM_005274742.2:c.*906T>G, XM_005274742.1:c.*906T>C, XM_005274742.1:c.*906T>G, XM_005274744.3:c.*906T>C, XM_005274744.3:c.*906T>G, XM_005274744.2:c.*906T>C, XM_005274744.2:c.*906T>G, XM_005274744.1:c.*906T>C, XM_005274744.1:c.*906T>G, XM_005274745.3:c.*906T>C, XM_005274745.3:c.*906T>G, XM_005274745.2:c.*906T>C, XM_005274745.2:c.*906T>G, XM_005274745.1:c.*906T>C, XM_005274745.1:c.*906T>G, XM_017029821.2:c.*906T>C, XM_017029821.2:c.*906T>G, XM_017029821.1:c.*906T>C, XM_017029821.1:c.*906T>G, XM_017029823.2:c.*906T>C, XM_017029823.2:c.*906T>G, XM_017029823.1:c.*906T>C, XM_017029823.1:c.*906T>G, XM_017029824.2:c.*906T>C, XM_017029824.2:c.*906T>G, XM_017029824.1:c.*906T>C, XM_017029824.1:c.*906T>G, XM_017029825.2:c.*906T>C, XM_017029825.2:c.*906T>G, XM_017029825.1:c.*906T>C, XM_017029825.1:c.*906T>G, XM_017029826.2:c.*906T>C, XM_017029826.2:c.*906T>G, XM_017029826.1:c.*906T>C, XM_017029826.1:c.*906T>G, XM_017029827.2:c.*906T>C, XM_017029827.2:c.*906T>G, XM_017029827.1:c.*906T>C, XM_017029827.1:c.*906T>G, XM_017029828.2:c.*906T>C, XM_017029828.2:c.*906T>G, XM_017029828.1:c.*906T>C, XM_017029828.1:c.*906T>G, XM_017029829.2:c.*906T>C, XM_017029829.2:c.*906T>G, XM_017029829.1:c.*906T>C, XM_017029829.1:c.*906T>G, XM_017029830.2:c.*906T>C, XM_017029830.2:c.*906T>G, XM_017029830.1:c.*906T>C, XM_017029830.1:c.*906T>G, XM_017029831.2:c.*906T>C, XM_017029831.2:c.*906T>G, XM_017029831.1:c.*906T>C, XM_017029831.1:c.*906T>G, XM_017029832.2:c.*906T>C, XM_017029832.2:c.*906T>G, XM_017029832.1:c.*906T>C, XM_017029832.1:c.*906T>G, XM_017029833.2:c.*906T>C, XM_017029833.2:c.*906T>G, XM_017029833.1:c.*906T>C, XM_017029833.1:c.*906T>G, XM_017029834.2:c.*906T>C, XM_017029834.2:c.*906T>G, XM_017029834.1:c.*906T>C, XM_017029834.1:c.*906T>G, XM_017029835.2:c.*906T>C, XM_017029835.2:c.*906T>G, XM_017029835.1:c.*906T>C, XM_017029835.1:c.*906T>G, XM_011531194.2:c.*906T>C, XM_011531194.2:c.*906T>G, XM_011531194.1:c.*906T>C, XM_011531194.1:c.*906T>G, XM_011531195.2:c.*906T>C, XM_011531195.2:c.*906T>G, XM_011531195.1:c.*906T>C, XM_011531195.1:c.*906T>G, XM_047442488.1:c.*906T>C, XM_047442488.1:c.*906T>G, XM_047442489.1:c.*906T>C, XM_047442489.1:c.*906T>G, XM_047442490.1:c.*906T>C, XM_047442490.1:c.*906T>G, XM_047442491.1:c.*906T>C, XM_047442491.1:c.*906T>G, XM_047442496.1:c.*906T>C, XM_047442496.1:c.*906T>G, XM_047442492.1:c.*906T>C, XM_047442492.1:c.*906T>G, XM_047442493.1:c.*906T>C, XM_047442493.1:c.*906T>G, XM_047442494.1:c.*906T>C, XM_047442494.1:c.*906T>G, XM_047442495.1:c.*906T>C, XM_047442495.1:c.*906T>G, XM_047442497.1:c.*906T>C, XM_047442497.1:c.*906T>G, XM_047442498.1:c.*906T>C, XM_047442498.1:c.*906T>G, XM_047442499.1:c.*906T>C, XM_047442499.1:c.*906T>G, XM_047442500.1:c.*906T>C, XM_047442500.1:c.*906T>G, XM_047442501.1:c.*906T>C, XM_047442501.1:c.*906T>G, XM_047442502.1:c.*906T>C, XM_047442502.1:c.*906T>G, XM_047442503.1:c.*906T>C, XM_047442503.1:c.*906T>G, XM_047442505.1:c.*906T>C, XM_047442505.1:c.*906T>G, XM_047442507.1:c.*906T>C, XM_047442507.1:c.*906T>G, XM_047442508.1:c.*906T>C, XM_047442508.1:c.*906T>G, XM_047442509.1:c.*906T>C, XM_047442509.1:c.*906T>G, NM_001178114.1:c.*906T>C, NM_001178114.1:c.*906T>G, XM_047442506.1:c.*906T>C, XM_047442506.1:c.*906T>G, XM_047442504.1:c.*906T>C, XM_047442504.1:c.*906T>G

                        12.

                        rs1480127802 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          X:152971612 (GRCh38)
                          X:152140156 (GRCh37)
                          Canonical SPDI:
                          NC_000023.11:152971611:G:A
                          Gene:
                          ZNF185 (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000019/2 (GnomAD)
                          A=0.000023/6 (TOPMED)
                          HGVS:
                          NC_000023.11:g.152971612G>A, NW_003871103.3:g.405595G>A, NG_021255.2:g.62171G>A, NM_007150.3:c.*339G>A, NM_001178108.2:c.*339G>A, NM_001178108.1:c.*339G>A, NM_001388432.2:c.*339G>A, NM_001388432.1:c.*339G>A, NM_001178113.2:c.*339G>A, NM_001178113.1:c.*339G>A, NM_001178115.2:c.*339G>A, NM_001178115.1:c.*339G>A, NM_001178106.1:c.*339G>A, NM_001395254.1:c.*339G>A, NM_001178107.1:c.*339G>A, NM_001178109.1:c.*339G>A, NM_001178110.1:c.*339G>A, NW_025791818.1:g.586802G>A, NC_000023.10:g.152140156G>A, XM_005274746.4:c.*339G>A, XM_005274746.3:c.*339G>A, XM_005274746.2:c.*339G>A, XM_005274746.1:c.*339G>A, XM_017029822.3:c.*339G>A, XM_017029822.2:c.*339G>A, XM_017029822.1:c.*339G>A, XM_005274738.3:c.*339G>A, XM_005274738.2:c.*339G>A, XM_005274738.1:c.*339G>A, XM_005274741.3:c.*339G>A, XM_005274741.2:c.*339G>A, XM_005274741.1:c.*339G>A, XM_005274740.3:c.*339G>A, XM_005274740.2:c.*339G>A, XM_005274740.1:c.*339G>A, XM_005274742.3:c.*339G>A, XM_005274742.2:c.*339G>A, XM_005274742.1:c.*339G>A, XM_005274744.3:c.*339G>A, XM_005274744.2:c.*339G>A, XM_005274744.1:c.*339G>A, XM_005274745.3:c.*339G>A, XM_005274745.2:c.*339G>A, XM_005274745.1:c.*339G>A, XM_017029821.2:c.*339G>A, XM_017029821.1:c.*339G>A, XM_017029823.2:c.*339G>A, XM_017029823.1:c.*339G>A, XM_017029824.2:c.*339G>A, XM_017029824.1:c.*339G>A, XM_017029825.2:c.*339G>A, XM_017029825.1:c.*339G>A, XM_017029826.2:c.*339G>A, XM_017029826.1:c.*339G>A, XM_017029827.2:c.*339G>A, XM_017029827.1:c.*339G>A, XM_017029828.2:c.*339G>A, XM_017029828.1:c.*339G>A, XM_017029829.2:c.*339G>A, XM_017029829.1:c.*339G>A, XM_017029830.2:c.*339G>A, XM_017029830.1:c.*339G>A, XM_017029831.2:c.*339G>A, XM_017029831.1:c.*339G>A, XM_017029832.2:c.*339G>A, XM_017029832.1:c.*339G>A, XM_017029833.2:c.*339G>A, XM_017029833.1:c.*339G>A, XM_017029834.2:c.*339G>A, XM_017029834.1:c.*339G>A, XM_017029835.2:c.*339G>A, XM_017029835.1:c.*339G>A, XM_011531194.2:c.*339G>A, XM_011531194.1:c.*339G>A, XM_011531195.2:c.*339G>A, XM_011531195.1:c.*339G>A, XM_047442488.1:c.*339G>A, XM_047442489.1:c.*339G>A, XM_047442490.1:c.*339G>A, XM_047442491.1:c.*339G>A, XM_047442496.1:c.*339G>A, XM_047442492.1:c.*339G>A, XM_047442493.1:c.*339G>A, XM_047442494.1:c.*339G>A, XM_047442495.1:c.*339G>A, XM_047442497.1:c.*339G>A, XM_047442498.1:c.*339G>A, XM_047442499.1:c.*339G>A, XM_047442500.1:c.*339G>A, XM_047442501.1:c.*339G>A, XM_047442502.1:c.*339G>A, XM_047442503.1:c.*339G>A, XM_047442505.1:c.*339G>A, XM_047442507.1:c.*339G>A, XM_047442508.1:c.*339G>A, XM_047442509.1:c.*339G>A, NM_001178114.1:c.*339G>A, XM_047442506.1:c.*339G>A, XM_047442504.1:c.*339G>A

                          13.

                          rs1480052016 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A,G,T [Show Flanks]
                            Chromosome:
                            X:152936457 (GRCh38)
                            X:152105001 (GRCh37)
                            Canonical SPDI:
                            NC_000023.11:152936456:C:A,NC_000023.11:152936456:C:G,NC_000023.11:152936456:C:T
                            Gene:
                            ZNF185 (Varview), LOC105373372 (Varview)
                            Functional Consequence:
                            intron_variant,genic_upstream_transcript_variant,missense_variant,synonymous_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            G=0./0 (ALFA)
                            HGVS:
                            NC_000023.11:g.152936457C>A, NC_000023.11:g.152936457C>G, NC_000023.11:g.152936457C>T, NW_003871103.3:g.370440C>A, NW_003871103.3:g.370440C>G, NW_003871103.3:g.370440C>T, NG_021255.2:g.27016C>A, NG_021255.2:g.27016C>G, NG_021255.2:g.27016C>T, NM_001178106.1:c.1158C>A, NM_001178106.1:c.1158C>G, NM_001178106.1:c.1158C>T, NM_001395254.1:c.1161C>A, NM_001395254.1:c.1161C>G, NM_001395254.1:c.1161C>T, NM_001178107.1:c.1071C>A, NM_001178107.1:c.1071C>G, NM_001178107.1:c.1071C>T, NW_025791818.1:g.551647C>A, NW_025791818.1:g.551647C>G, NW_025791818.1:g.551647C>T, NC_000023.10:g.152105001C>A, NC_000023.10:g.152105001C>G, NC_000023.10:g.152105001C>T, XM_017029822.3:c.1161C>A, XM_017029822.3:c.1161C>G, XM_017029822.3:c.1161C>T, XM_017029822.2:c.1161C>A, XM_017029822.2:c.1161C>G, XM_017029822.2:c.1161C>T, XM_017029822.1:c.1161C>A, XM_017029822.1:c.1161C>G, XM_017029822.1:c.1161C>T, XM_017029821.2:c.1161C>A, XM_017029821.2:c.1161C>G, XM_017029821.2:c.1161C>T, XM_017029821.1:c.1161C>A, XM_017029821.1:c.1161C>G, XM_017029821.1:c.1161C>T, XM_017029823.2:c.1158C>A, XM_017029823.2:c.1158C>G, XM_017029823.2:c.1158C>T, XM_017029823.1:c.1158C>A, XM_017029823.1:c.1158C>G, XM_017029823.1:c.1158C>T, XM_017029824.2:c.1077C>A, XM_017029824.2:c.1077C>G, XM_017029824.2:c.1077C>T, XM_017029824.1:c.1077C>A, XM_017029824.1:c.1077C>G, XM_017029824.1:c.1077C>T, XM_017029825.2:c.1074C>A, XM_017029825.2:c.1074C>G, XM_017029825.2:c.1074C>T, XM_017029825.1:c.1074C>A, XM_017029825.1:c.1074C>G, XM_017029825.1:c.1074C>T, XM_017029826.2:c.1071C>A, XM_017029826.2:c.1071C>G, XM_017029826.2:c.1071C>T, XM_017029826.1:c.1071C>A, XM_017029826.1:c.1071C>G, XM_017029826.1:c.1071C>T, XM_017029827.2:c.1068C>A, XM_017029827.2:c.1068C>G, XM_017029827.2:c.1068C>T, XM_017029827.1:c.1068C>A, XM_017029827.1:c.1068C>G, XM_017029827.1:c.1068C>T, XM_017029829.2:c.984C>A, XM_017029829.2:c.984C>G, XM_017029829.2:c.984C>T, XM_017029829.1:c.984C>A, XM_017029829.1:c.984C>G, XM_017029829.1:c.984C>T, XM_017029833.2:c.900C>A, XM_017029833.2:c.900C>G, XM_017029833.2:c.900C>T, XM_017029833.1:c.900C>A, XM_017029833.1:c.900C>G, XM_017029833.1:c.900C>T, XM_017029835.2:c.981C>A, XM_017029835.2:c.981C>G, XM_017029835.2:c.981C>T, XM_017029835.1:c.981C>A, XM_017029835.1:c.981C>G, XM_017029835.1:c.981C>T, XM_011531195.2:c.1161C>A, XM_011531195.2:c.1161C>G, XM_011531195.2:c.1161C>T, XM_011531195.1:c.1161C>A, XM_011531195.1:c.1161C>G, XM_011531195.1:c.1161C>T, XM_047442490.1:c.1074C>A, XM_047442490.1:c.1074C>G, XM_047442490.1:c.1074C>T, XM_047442491.1:c.1071C>A, XM_047442491.1:c.1071C>G, XM_047442491.1:c.1071C>T, XM_047442492.1:c.987C>A, XM_047442492.1:c.987C>G, XM_047442492.1:c.987C>T, XM_047442493.1:c.984C>A, XM_047442493.1:c.984C>G, XM_047442493.1:c.984C>T, XM_047442504.1:c.984C>A, XM_047442504.1:c.984C>G, XM_047442504.1:c.984C>T, NP_001171577.1:p.Asp386Glu, NP_001171577.1:p.Asp386Glu, NP_001382183.1:p.Asp387Glu, NP_001382183.1:p.Asp387Glu, NP_001171578.1:p.Asp357Glu, NP_001171578.1:p.Asp357Glu, XP_016885311.1:p.Asp387Glu, XP_016885311.1:p.Asp387Glu, XP_016885310.1:p.Asp387Glu, XP_016885310.1:p.Asp387Glu, XP_016885312.1:p.Asp386Glu, XP_016885312.1:p.Asp386Glu, XP_016885313.1:p.Asp359Glu, XP_016885313.1:p.Asp359Glu, XP_016885314.1:p.Asp358Glu, XP_016885314.1:p.Asp358Glu, XP_016885315.1:p.Asp357Glu, XP_016885315.1:p.Asp357Glu, XP_016885316.1:p.Asp356Glu, XP_016885316.1:p.Asp356Glu, XP_016885318.1:p.Asp328Glu, XP_016885318.1:p.Asp328Glu, XP_016885322.1:p.Asp300Glu, XP_016885322.1:p.Asp300Glu, XP_016885324.1:p.Asp327Glu, XP_016885324.1:p.Asp327Glu, XP_011529497.1:p.Asp387Glu, XP_011529497.1:p.Asp387Glu, XP_047298446.1:p.Asp358Glu, XP_047298446.1:p.Asp358Glu, XP_047298447.1:p.Asp357Glu, XP_047298447.1:p.Asp357Glu, XP_047298448.1:p.Asp329Glu, XP_047298448.1:p.Asp329Glu, XP_047298449.1:p.Asp328Glu, XP_047298449.1:p.Asp328Glu, XP_047298460.1:p.Asp328Glu, XP_047298460.1:p.Asp328Glu

                            14.

                            rs1476861381 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>G [Show Flanks]
                              Chromosome:
                              X:152972810 (GRCh38)
                              X:152141354 (GRCh37)
                              Canonical SPDI:
                              NC_000023.11:152972809:A:G
                              Gene:
                              ZNF185 (Varview)
                              Functional Consequence:
                              3_prime_UTR_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000008/2 (TOPMED)
                              G=0.000019/2 (GnomAD)
                              HGVS:
                              NC_000023.11:g.152972810A>G, NW_003871103.3:g.406793A>G, NG_021255.2:g.63369A>G, NM_007150.3:c.*1537A>G, NM_001178108.2:c.*1537A>G, NM_001178108.1:c.*1537A>G, NM_001388432.2:c.*1537A>G, NM_001388432.1:c.*1537A>G, NM_001178113.2:c.*1537A>G, NM_001178113.1:c.*1537A>G, NM_001178115.2:c.*1537A>G, NM_001178115.1:c.*1537A>G, NM_001178106.1:c.*1537A>G, NM_001395254.1:c.*1537A>G, NM_001178107.1:c.*1537A>G, NM_001178109.1:c.*1537A>G, NM_001178110.1:c.*1537A>G, NW_025791818.1:g.588000A>G, NC_000023.10:g.152141354A>G, XM_005274746.4:c.*1537A>G, XM_005274746.3:c.*1537A>G, XM_005274746.2:c.*1537A>G, XM_005274746.1:c.*1537A>G, XM_017029822.3:c.*1537A>G, XM_017029822.2:c.*1537A>G, XM_017029822.1:c.*1537A>G, XM_005274738.3:c.*1537A>G, XM_005274738.2:c.*1537A>G, XM_005274738.1:c.*1537A>G, XM_005274741.3:c.*1537A>G, XM_005274741.2:c.*1537A>G, XM_005274741.1:c.*1537A>G, XM_005274740.3:c.*1537A>G, XM_005274740.2:c.*1537A>G, XM_005274740.1:c.*1537A>G, XM_005274742.3:c.*1537A>G, XM_005274742.2:c.*1537A>G, XM_005274742.1:c.*1537A>G, XM_005274744.3:c.*1537A>G, XM_005274744.2:c.*1537A>G, XM_005274744.1:c.*1537A>G, XM_005274745.3:c.*1537A>G, XM_005274745.2:c.*1537A>G, XM_005274745.1:c.*1537A>G, XM_017029821.2:c.*1537A>G, XM_017029821.1:c.*1537A>G, XM_017029823.2:c.*1537A>G, XM_017029823.1:c.*1537A>G, XM_017029824.2:c.*1537A>G, XM_017029824.1:c.*1537A>G, XM_017029825.2:c.*1537A>G, XM_017029825.1:c.*1537A>G, XM_017029826.2:c.*1537A>G, XM_017029826.1:c.*1537A>G, XM_017029827.2:c.*1537A>G, XM_017029827.1:c.*1537A>G, XM_017029828.2:c.*1537A>G, XM_017029828.1:c.*1537A>G, XM_017029829.2:c.*1537A>G, XM_017029829.1:c.*1537A>G, XM_017029830.2:c.*1537A>G, XM_017029830.1:c.*1537A>G, XM_017029831.2:c.*1537A>G, XM_017029831.1:c.*1537A>G, XM_017029832.2:c.*1537A>G, XM_017029832.1:c.*1537A>G, XM_017029833.2:c.*1537A>G, XM_017029833.1:c.*1537A>G, XM_017029834.2:c.*1537A>G, XM_017029834.1:c.*1537A>G, XM_017029835.2:c.*1537A>G, XM_017029835.1:c.*1537A>G, XM_011531194.2:c.*1537A>G, XM_011531194.1:c.*1537A>G, XM_011531195.2:c.*1537A>G, XM_011531195.1:c.*1537A>G, XM_047442488.1:c.*1537A>G, XM_047442489.1:c.*1537A>G, XM_047442490.1:c.*1537A>G, XM_047442491.1:c.*1537A>G, XM_047442496.1:c.*1537A>G, XM_047442492.1:c.*1537A>G, XM_047442493.1:c.*1537A>G, XM_047442494.1:c.*1537A>G, XM_047442495.1:c.*1537A>G, XM_047442497.1:c.*1537A>G, XM_047442498.1:c.*1537A>G, XM_047442499.1:c.*1537A>G, XM_047442500.1:c.*1537A>G, XM_047442501.1:c.*1537A>G, XM_047442502.1:c.*1537A>G, XM_047442503.1:c.*1537A>G, XM_047442505.1:c.*1537A>G, XM_047442507.1:c.*1537A>G, XM_047442508.1:c.*1537A>G, XM_047442509.1:c.*1537A>G, NM_001178114.1:c.*1537A>G, XM_047442506.1:c.*1537A>G, XM_047442504.1:c.*1537A>G

                              15.

                              rs1475396004 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>T [Show Flanks]
                                Chromosome:
                                X:152972626 (GRCh38)
                                X:152141170 (GRCh37)
                                Canonical SPDI:
                                NC_000023.11:152972625:G:T
                                Gene:
                                ZNF185 (Varview)
                                Functional Consequence:
                                3_prime_UTR_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                T=0.00001/1 (GnomAD)
                                HGVS:
                                NC_000023.11:g.152972626G>T, NW_003871103.3:g.406609G>T, NG_021255.2:g.63185G>T, NM_007150.3:c.*1353G>T, NM_001178108.2:c.*1353G>T, NM_001178108.1:c.*1353G>T, NM_001388432.2:c.*1353G>T, NM_001388432.1:c.*1353G>T, NM_001178113.2:c.*1353G>T, NM_001178113.1:c.*1353G>T, NM_001178115.2:c.*1353G>T, NM_001178115.1:c.*1353G>T, NM_001178106.1:c.*1353G>T, NM_001395254.1:c.*1353G>T, NM_001178107.1:c.*1353G>T, NM_001178109.1:c.*1353G>T, NM_001178110.1:c.*1353G>T, NW_025791818.1:g.587816G>T, NC_000023.10:g.152141170G>T, XM_005274746.4:c.*1353G>T, XM_005274746.3:c.*1353G>T, XM_005274746.2:c.*1353G>T, XM_005274746.1:c.*1353G>T, XM_017029822.3:c.*1353G>T, XM_017029822.2:c.*1353G>T, XM_017029822.1:c.*1353G>T, XM_005274738.3:c.*1353G>T, XM_005274738.2:c.*1353G>T, XM_005274738.1:c.*1353G>T, XM_005274741.3:c.*1353G>T, XM_005274741.2:c.*1353G>T, XM_005274741.1:c.*1353G>T, XM_005274740.3:c.*1353G>T, XM_005274740.2:c.*1353G>T, XM_005274740.1:c.*1353G>T, XM_005274742.3:c.*1353G>T, XM_005274742.2:c.*1353G>T, XM_005274742.1:c.*1353G>T, XM_005274744.3:c.*1353G>T, XM_005274744.2:c.*1353G>T, XM_005274744.1:c.*1353G>T, XM_005274745.3:c.*1353G>T, XM_005274745.2:c.*1353G>T, XM_005274745.1:c.*1353G>T, XM_017029821.2:c.*1353G>T, XM_017029821.1:c.*1353G>T, XM_017029823.2:c.*1353G>T, XM_017029823.1:c.*1353G>T, XM_017029824.2:c.*1353G>T, XM_017029824.1:c.*1353G>T, XM_017029825.2:c.*1353G>T, XM_017029825.1:c.*1353G>T, XM_017029826.2:c.*1353G>T, XM_017029826.1:c.*1353G>T, XM_017029827.2:c.*1353G>T, XM_017029827.1:c.*1353G>T, XM_017029828.2:c.*1353G>T, XM_017029828.1:c.*1353G>T, XM_017029829.2:c.*1353G>T, XM_017029829.1:c.*1353G>T, XM_017029830.2:c.*1353G>T, XM_017029830.1:c.*1353G>T, XM_017029831.2:c.*1353G>T, XM_017029831.1:c.*1353G>T, XM_017029832.2:c.*1353G>T, XM_017029832.1:c.*1353G>T, XM_017029833.2:c.*1353G>T, XM_017029833.1:c.*1353G>T, XM_017029834.2:c.*1353G>T, XM_017029834.1:c.*1353G>T, XM_017029835.2:c.*1353G>T, XM_017029835.1:c.*1353G>T, XM_011531194.2:c.*1353G>T, XM_011531194.1:c.*1353G>T, XM_011531195.2:c.*1353G>T, XM_011531195.1:c.*1353G>T, XM_047442488.1:c.*1353G>T, XM_047442489.1:c.*1353G>T, XM_047442490.1:c.*1353G>T, XM_047442491.1:c.*1353G>T, XM_047442496.1:c.*1353G>T, XM_047442492.1:c.*1353G>T, XM_047442493.1:c.*1353G>T, XM_047442494.1:c.*1353G>T, XM_047442495.1:c.*1353G>T, XM_047442497.1:c.*1353G>T, XM_047442498.1:c.*1353G>T, XM_047442499.1:c.*1353G>T, XM_047442500.1:c.*1353G>T, XM_047442501.1:c.*1353G>T, XM_047442502.1:c.*1353G>T, XM_047442503.1:c.*1353G>T, XM_047442505.1:c.*1353G>T, XM_047442507.1:c.*1353G>T, XM_047442508.1:c.*1353G>T, XM_047442509.1:c.*1353G>T, NM_001178114.1:c.*1353G>T, XM_047442506.1:c.*1353G>T, XM_047442504.1:c.*1353G>T

                                16.

                                rs1475297480 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>G [Show Flanks]
                                  Chromosome:
                                  X:152971766 (GRCh38)
                                  X:152140310 (GRCh37)
                                  Canonical SPDI:
                                  NC_000023.11:152971765:A:G
                                  Gene:
                                  ZNF185 (Varview)
                                  Functional Consequence:
                                  3_prime_UTR_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000042/11 (TOPMED)
                                  HGVS:
                                  NC_000023.11:g.152971766A>G, NW_003871103.3:g.405749A>G, NG_021255.2:g.62325A>G, NM_007150.3:c.*493A>G, NM_001178108.2:c.*493A>G, NM_001178108.1:c.*493A>G, NM_001388432.2:c.*493A>G, NM_001388432.1:c.*493A>G, NM_001178113.2:c.*493A>G, NM_001178113.1:c.*493A>G, NM_001178115.2:c.*493A>G, NM_001178115.1:c.*493A>G, NM_001178106.1:c.*493A>G, NM_001395254.1:c.*493A>G, NM_001178107.1:c.*493A>G, NM_001178109.1:c.*493A>G, NM_001178110.1:c.*493A>G, NW_025791818.1:g.586956A>G, NC_000023.10:g.152140310A>G, XM_005274746.4:c.*493A>G, XM_005274746.3:c.*493A>G, XM_005274746.2:c.*493A>G, XM_005274746.1:c.*493A>G, XM_017029822.3:c.*493A>G, XM_017029822.2:c.*493A>G, XM_017029822.1:c.*493A>G, XM_005274738.3:c.*493A>G, XM_005274738.2:c.*493A>G, XM_005274738.1:c.*493A>G, XM_005274741.3:c.*493A>G, XM_005274741.2:c.*493A>G, XM_005274741.1:c.*493A>G, XM_005274740.3:c.*493A>G, XM_005274740.2:c.*493A>G, XM_005274740.1:c.*493A>G, XM_005274742.3:c.*493A>G, XM_005274742.2:c.*493A>G, XM_005274742.1:c.*493A>G, XM_005274744.3:c.*493A>G, XM_005274744.2:c.*493A>G, XM_005274744.1:c.*493A>G, XM_005274745.3:c.*493A>G, XM_005274745.2:c.*493A>G, XM_005274745.1:c.*493A>G, XM_017029821.2:c.*493A>G, XM_017029821.1:c.*493A>G, XM_017029823.2:c.*493A>G, XM_017029823.1:c.*493A>G, XM_017029824.2:c.*493A>G, XM_017029824.1:c.*493A>G, XM_017029825.2:c.*493A>G, XM_017029825.1:c.*493A>G, XM_017029826.2:c.*493A>G, XM_017029826.1:c.*493A>G, XM_017029827.2:c.*493A>G, XM_017029827.1:c.*493A>G, XM_017029828.2:c.*493A>G, XM_017029828.1:c.*493A>G, XM_017029829.2:c.*493A>G, XM_017029829.1:c.*493A>G, XM_017029830.2:c.*493A>G, XM_017029830.1:c.*493A>G, XM_017029831.2:c.*493A>G, XM_017029831.1:c.*493A>G, XM_017029832.2:c.*493A>G, XM_017029832.1:c.*493A>G, XM_017029833.2:c.*493A>G, XM_017029833.1:c.*493A>G, XM_017029834.2:c.*493A>G, XM_017029834.1:c.*493A>G, XM_017029835.2:c.*493A>G, XM_017029835.1:c.*493A>G, XM_011531194.2:c.*493A>G, XM_011531194.1:c.*493A>G, XM_011531195.2:c.*493A>G, XM_011531195.1:c.*493A>G, XM_047442488.1:c.*493A>G, XM_047442489.1:c.*493A>G, XM_047442490.1:c.*493A>G, XM_047442491.1:c.*493A>G, XM_047442496.1:c.*493A>G, XM_047442492.1:c.*493A>G, XM_047442493.1:c.*493A>G, XM_047442494.1:c.*493A>G, XM_047442495.1:c.*493A>G, XM_047442497.1:c.*493A>G, XM_047442498.1:c.*493A>G, XM_047442499.1:c.*493A>G, XM_047442500.1:c.*493A>G, XM_047442501.1:c.*493A>G, XM_047442502.1:c.*493A>G, XM_047442503.1:c.*493A>G, XM_047442505.1:c.*493A>G, XM_047442507.1:c.*493A>G, XM_047442508.1:c.*493A>G, XM_047442509.1:c.*493A>G, NM_001178114.1:c.*493A>G, XM_047442506.1:c.*493A>G, XM_047442504.1:c.*493A>G

                                  17.

                                  rs1474265570 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>G [Show Flanks]
                                    Chromosome:
                                    X:152936439 (GRCh38)
                                    X:152104983 (GRCh37)
                                    Canonical SPDI:
                                    NC_000023.11:152936438:T:G
                                    Gene:
                                    ZNF185 (Varview), LOC105373372 (Varview)
                                    Functional Consequence:
                                    genic_upstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000004/1 (TOPMED)
                                    G=0.00001/1 (GnomAD)
                                    HGVS:
                                    NC_000023.11:g.152936439T>G, NW_003871103.3:g.370422T>G, NG_021255.2:g.26998T>G, NM_001178106.1:c.1140T>G, NM_001395254.1:c.1143T>G, NM_001178107.1:c.1053T>G, NW_025791818.1:g.551629T>G, NC_000023.10:g.152104983T>G, XM_017029822.3:c.1143T>G, XM_017029822.2:c.1143T>G, XM_017029822.1:c.1143T>G, XM_017029821.2:c.1143T>G, XM_017029821.1:c.1143T>G, XM_017029823.2:c.1140T>G, XM_017029823.1:c.1140T>G, XM_017029824.2:c.1059T>G, XM_017029824.1:c.1059T>G, XM_017029825.2:c.1056T>G, XM_017029825.1:c.1056T>G, XM_017029826.2:c.1053T>G, XM_017029826.1:c.1053T>G, XM_017029827.2:c.1050T>G, XM_017029827.1:c.1050T>G, XM_017029829.2:c.966T>G, XM_017029829.1:c.966T>G, XM_017029833.2:c.882T>G, XM_017029833.1:c.882T>G, XM_017029835.2:c.963T>G, XM_017029835.1:c.963T>G, XM_011531195.2:c.1143T>G, XM_011531195.1:c.1143T>G, XM_047442490.1:c.1056T>G, XM_047442491.1:c.1053T>G, XM_047442492.1:c.969T>G, XM_047442493.1:c.966T>G, XM_047442504.1:c.966T>G, NP_001171577.1:p.Phe380Leu, NP_001382183.1:p.Phe381Leu, NP_001171578.1:p.Phe351Leu, XP_016885311.1:p.Phe381Leu, XP_016885310.1:p.Phe381Leu, XP_016885312.1:p.Phe380Leu, XP_016885313.1:p.Phe353Leu, XP_016885314.1:p.Phe352Leu, XP_016885315.1:p.Phe351Leu, XP_016885316.1:p.Phe350Leu, XP_016885318.1:p.Phe322Leu, XP_016885322.1:p.Phe294Leu, XP_016885324.1:p.Phe321Leu, XP_011529497.1:p.Phe381Leu, XP_047298446.1:p.Phe352Leu, XP_047298447.1:p.Phe351Leu, XP_047298448.1:p.Phe323Leu, XP_047298449.1:p.Phe322Leu, XP_047298460.1:p.Phe322Leu

                                    18.

                                    rs1472617001 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      CAGGAGAGGCCTGG>-,CAGGAGAGGCCTGGCAGGAGAGGCCTGG [Show Flanks]
                                      Chromosome:
                                      X:152945322 (GRCh38)
                                      X:152113866 (GRCh37)
                                      Canonical SPDI:
                                      NC_000023.11:152945309:GGAGAGGCCTGGCAGGAGAGGCCTGG:GGAGAGGCCTGG,NC_000023.11:152945309:GGAGAGGCCTGGCAGGAGAGGCCTGG:GGAGAGGCCTGGCAGGAGAGGCCTGGCAGGAGAGGCCTGG
                                      Gene:
                                      ZNF185 (Varview)
                                      Functional Consequence:
                                      frameshift_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      GGAGAGGCCTGGCAGGAGAGGCCTGGCAGGAGAGGCCTGG=0./0 (ALFA)
                                      GGAGAGGCCTGGCA=0.00001/1 (GnomAD)
                                      HGVS:
                                      NC_000023.11:g.152945322_152945335del, NC_000023.11:g.152945322_152945335dup, NW_003871103.3:g.379305_379318del, NW_003871103.3:g.379305_379318dup, NG_021255.2:g.35881_35894del, NG_021255.2:g.35881_35894dup, NM_007150.3:c.1264_1277del, NM_007150.3:c.1264_1277dup, NM_001178108.2:c.1267_1280del, NM_001178108.2:c.1267_1280dup, NM_001178108.1:c.1267_1280del, NM_001178108.1:c.1267_1280dup, NM_001388432.2:c.1267_1280del, NM_001388432.2:c.1267_1280dup, NM_001388432.1:c.1267_1280del, NM_001388432.1:c.1267_1280dup, NM_001178113.2:c.601_614del, NM_001178113.2:c.601_614dup, NM_001178113.1:c.601_614del, NM_001178113.1:c.601_614dup, NM_001178115.2:c.178_191del, NM_001178115.2:c.178_191dup, NM_001178115.1:c.178_191del, NM_001178115.1:c.178_191dup, NM_001178106.1:c.1360_1373del, NM_001178106.1:c.1360_1373dup, NM_001395254.1:c.1363_1376del, NM_001395254.1:c.1363_1376dup, NM_001178107.1:c.1273_1286del, NM_001178107.1:c.1273_1286dup, NM_001178109.1:c.1177_1190del, NM_001178109.1:c.1177_1190dup, NM_001178110.1:c.1087_1100del, NM_001178110.1:c.1087_1100dup, NW_025791818.1:g.560512_560525del, NW_025791818.1:g.560512_560525dup, NC_000023.10:g.152113866_152113879del, NC_000023.10:g.152113866_152113879dup, XM_005274746.4:c.1006_1019del, XM_005274746.4:c.1006_1019dup, XM_005274746.3:c.1006_1019del, XM_005274746.3:c.1006_1019dup, XM_005274746.2:c.1006_1019del, XM_005274746.2:c.1006_1019dup, XM_005274746.1:c.1006_1019del, XM_005274746.1:c.1006_1019dup, XM_017029822.3:c.1363_1376del, XM_017029822.3:c.1363_1376dup, XM_017029822.2:c.1363_1376del, XM_017029822.2:c.1363_1376dup, XM_017029822.1:c.1363_1376del, XM_017029822.1:c.1363_1376dup, XM_005274738.3:c.1264_1277del, XM_005274738.3:c.1264_1277dup, XM_005274738.2:c.1264_1277del, XM_005274738.2:c.1264_1277dup, XM_005274738.1:c.1264_1277del, XM_005274738.1:c.1264_1277dup, XM_005274741.3:c.1177_1190del, XM_005274741.3:c.1177_1190dup, XM_005274741.2:c.1177_1190del, XM_005274741.2:c.1177_1190dup, XM_005274741.1:c.1177_1190del, XM_005274741.1:c.1177_1190dup, XM_005274740.3:c.1177_1190del, XM_005274740.3:c.1177_1190dup, XM_005274740.2:c.1177_1190del, XM_005274740.2:c.1177_1190dup, XM_005274740.1:c.1177_1190del, XM_005274740.1:c.1177_1190dup, XM_005274742.3:c.1174_1187del, XM_005274742.3:c.1174_1187dup, XM_005274742.2:c.1174_1187del, XM_005274742.2:c.1174_1187dup, XM_005274742.1:c.1174_1187del, XM_005274742.1:c.1174_1187dup, XM_005274744.3:c.1090_1103del, XM_005274744.3:c.1090_1103dup, XM_005274744.2:c.1090_1103del, XM_005274744.2:c.1090_1103dup, XM_005274744.1:c.1090_1103del, XM_005274744.1:c.1090_1103dup, XM_005274745.3:c.1087_1100del, XM_005274745.3:c.1087_1100dup, XM_005274745.2:c.1087_1100del, XM_005274745.2:c.1087_1100dup, XM_005274745.1:c.1087_1100del, XM_005274745.1:c.1087_1100dup, XM_017029821.2:c.1363_1376del, XM_017029821.2:c.1363_1376dup, XM_017029821.1:c.1363_1376del, XM_017029821.1:c.1363_1376dup, XM_017029823.2:c.1360_1373del, XM_017029823.2:c.1360_1373dup, XM_017029823.1:c.1360_1373del, XM_017029823.1:c.1360_1373dup, XM_017029824.2:c.1279_1292del, XM_017029824.2:c.1279_1292dup, XM_017029824.1:c.1279_1292del, XM_017029824.1:c.1279_1292dup, XM_017029825.2:c.1276_1289del, XM_017029825.2:c.1276_1289dup, XM_017029825.1:c.1276_1289del, XM_017029825.1:c.1276_1289dup, XM_017029826.2:c.1273_1286del, XM_017029826.2:c.1273_1286dup, XM_017029826.1:c.1273_1286del, XM_017029826.1:c.1273_1286dup, XM_017029827.2:c.1270_1283del, XM_017029827.2:c.1270_1283dup, XM_017029827.1:c.1270_1283del, XM_017029827.1:c.1270_1283dup, XM_017029828.2:c.1267_1280del, XM_017029828.2:c.1267_1280dup, XM_017029828.1:c.1267_1280del, XM_017029828.1:c.1267_1280dup, XM_017029829.2:c.1186_1199del, XM_017029829.2:c.1186_1199dup, XM_017029829.1:c.1186_1199del, XM_017029829.1:c.1186_1199dup, XM_017029830.2:c.1180_1193del, XM_017029830.2:c.1180_1193dup, XM_017029830.1:c.1180_1193del, XM_017029830.1:c.1180_1193dup, XM_017029831.2:c.1177_1190del, XM_017029831.2:c.1177_1190dup, XM_017029831.1:c.1177_1190del, XM_017029831.1:c.1177_1190dup, XM_017029832.2:c.1168_1181del, XM_017029832.2:c.1168_1181dup, XM_017029832.1:c.1168_1181del, XM_017029832.1:c.1168_1181dup, XM_017029833.2:c.1102_1115del, XM_017029833.2:c.1102_1115dup, XM_017029833.1:c.1102_1115del, XM_017029833.1:c.1102_1115dup, XM_017029834.2:c.1090_1103del, XM_017029834.2:c.1090_1103dup, XM_017029834.1:c.1090_1103del, XM_017029834.1:c.1090_1103dup, XM_017029835.2:c.1183_1196del, XM_017029835.2:c.1183_1196dup, XM_017029835.1:c.1183_1196del, XM_017029835.1:c.1183_1196dup, XM_011531194.2:c.1168_1181del, XM_011531194.2:c.1168_1181dup, XM_011531194.1:c.1168_1181del, XM_011531194.1:c.1168_1181dup, XM_011531195.2:c.1363_1376del, XM_011531195.2:c.1363_1376dup, XM_011531195.1:c.1363_1376del, XM_011531195.1:c.1363_1376dup, XM_047442488.1:c.1264_1277del, XM_047442488.1:c.1264_1277dup, XM_047442489.1:c.1174_1187del, XM_047442489.1:c.1174_1187dup, XM_047442490.1:c.1276_1289del, XM_047442490.1:c.1276_1289dup, XM_047442491.1:c.1273_1286del, XM_047442491.1:c.1273_1286dup, XM_047442496.1:c.1177_1190del, XM_047442496.1:c.1177_1190dup, XM_047442492.1:c.1189_1202del, XM_047442492.1:c.1189_1202dup, XM_047442493.1:c.1186_1199del, XM_047442493.1:c.1186_1199dup, XM_047442494.1:c.1183_1196del, XM_047442494.1:c.1183_1196dup, XM_047442495.1:c.1180_1193del, XM_047442495.1:c.1180_1193dup, XM_047442497.1:c.1165_1178del, XM_047442497.1:c.1165_1178dup, XM_047442498.1:c.1096_1109del, XM_047442498.1:c.1096_1109dup, XM_047442499.1:c.1093_1106del, XM_047442499.1:c.1093_1106dup, XM_047442500.1:c.1081_1094del, XM_047442500.1:c.1081_1094dup, XM_047442501.1:c.1267_1280del, XM_047442501.1:c.1267_1280dup, XM_047442502.1:c.1264_1277del, XM_047442502.1:c.1264_1277dup, XM_047442503.1:c.991_1004del, XM_047442503.1:c.991_1004dup, XM_047442505.1:c.988_1001del, XM_047442505.1:c.988_1001dup, XM_047442507.1:c.1177_1190del, XM_047442507.1:c.1177_1190dup, XM_047442508.1:c.907_920del, XM_047442508.1:c.907_920dup, XM_047442509.1:c.1090_1103del, XM_047442509.1:c.1090_1103dup, NM_001178114.1:c.553_566del, NM_001178114.1:c.553_566dup, XM_047442506.1:c.1180_1193del, XM_047442506.1:c.1180_1193dup, XM_047442504.1:c.1186_1199del, XM_047442504.1:c.1186_1199dup, NP_009081.2:p.Gln422fs, NP_009081.2:p.Ala427fs, NP_001171579.1:p.Gln423fs, NP_001171579.1:p.Ala428fs, NP_001375361.1:p.Gln423fs, NP_001375361.1:p.Ala428fs, NP_001171584.1:p.Gln201fs, NP_001171584.1:p.Ala206fs, NP_001171586.1:p.Gln60fs, NP_001171586.1:p.Ala65fs, NP_001171577.1:p.Gln454fs, NP_001171577.1:p.Ala459fs, NP_001382183.1:p.Gln455fs, NP_001382183.1:p.Ala460fs, NP_001171578.1:p.Gln425fs, NP_001171578.1:p.Ala430fs, NP_001171580.1:p.Gln393fs, NP_001171580.1:p.Ala398fs, NP_001171581.1:p.Gln363fs, NP_001171581.1:p.Ala368fs, XP_005274803.1:p.Gln336fs, XP_005274803.1:p.Ala341fs, XP_016885311.1:p.Gln455fs, XP_016885311.1:p.Ala460fs, XP_005274795.1:p.Gln422fs, XP_005274795.1:p.Ala427fs, XP_005274798.1:p.Gln393fs, XP_005274798.1:p.Ala398fs, XP_005274797.1:p.Gln393fs, XP_005274797.1:p.Ala398fs, XP_005274799.1:p.Gln392fs, XP_005274799.1:p.Ala397fs, XP_005274801.1:p.Gln364fs, XP_005274801.1:p.Ala369fs, XP_005274802.1:p.Gln363fs, XP_005274802.1:p.Ala368fs, XP_016885310.1:p.Gln455fs, XP_016885310.1:p.Ala460fs, XP_016885312.1:p.Gln454fs, XP_016885312.1:p.Ala459fs, XP_016885313.1:p.Gln427fs, XP_016885313.1:p.Ala432fs, XP_016885314.1:p.Gln426fs, XP_016885314.1:p.Ala431fs, XP_016885315.1:p.Gln425fs, XP_016885315.1:p.Ala430fs, XP_016885316.1:p.Gln424fs, XP_016885316.1:p.Ala429fs, XP_016885317.1:p.Gln423fs, XP_016885317.1:p.Ala428fs, XP_016885318.1:p.Gln396fs, XP_016885318.1:p.Ala401fs, XP_016885319.1:p.Gln394fs, XP_016885319.1:p.Ala399fs, XP_016885320.1:p.Gln393fs, XP_016885320.1:p.Ala398fs, XP_016885321.1:p.Gln390fs, XP_016885321.1:p.Ala395fs, XP_016885322.1:p.Gln368fs, XP_016885322.1:p.Ala373fs, XP_016885323.1:p.Gln364fs, XP_016885323.1:p.Ala369fs, XP_016885324.1:p.Gln395fs, XP_016885324.1:p.Ala400fs, XP_011529496.1:p.Gln390fs, XP_011529496.1:p.Ala395fs, XP_011529497.1:p.Gln455fs, XP_011529497.1:p.Ala460fs, XP_047298444.1:p.Gln422fs, XP_047298444.1:p.Ala427fs, XP_047298445.1:p.Gln392fs, XP_047298445.1:p.Ala397fs, XP_047298446.1:p.Gln426fs, XP_047298446.1:p.Ala431fs, XP_047298447.1:p.Gln425fs, XP_047298447.1:p.Ala430fs, XP_047298452.1:p.Gln393fs, XP_047298452.1:p.Ala398fs, XP_047298448.1:p.Gln397fs, XP_047298448.1:p.Ala402fs, XP_047298449.1:p.Gln396fs, XP_047298449.1:p.Ala401fs, XP_047298450.1:p.Gln395fs, XP_047298450.1:p.Ala400fs, XP_047298451.1:p.Gln394fs, XP_047298451.1:p.Ala399fs, XP_047298453.1:p.Gln389fs, XP_047298453.1:p.Ala394fs, XP_047298454.1:p.Gln366fs, XP_047298454.1:p.Ala371fs, XP_047298455.1:p.Gln365fs, XP_047298455.1:p.Ala370fs, XP_047298456.1:p.Gln361fs, XP_047298456.1:p.Ala366fs, XP_047298457.1:p.Gln423fs, XP_047298457.1:p.Ala428fs, XP_047298458.1:p.Gln422fs, XP_047298458.1:p.Ala427fs, XP_047298459.1:p.Gln331fs, XP_047298459.1:p.Ala336fs, XP_047298461.1:p.Gln330fs, XP_047298461.1:p.Ala335fs, XP_047298463.1:p.Gln393fs, XP_047298463.1:p.Ala398fs, XP_047298464.1:p.Gln303fs, XP_047298464.1:p.Ala308fs, XP_047298465.1:p.Gln364fs, XP_047298465.1:p.Ala369fs, XP_047298462.1:p.Gln394fs, XP_047298462.1:p.Ala399fs, XP_047298460.1:p.Gln396fs, XP_047298460.1:p.Ala401fs

                                      19.

                                      rs1472050438 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        X:152972965 (GRCh38)
                                        X:152141509 (GRCh37)
                                        Canonical SPDI:
                                        NC_000023.11:152972964:G:A
                                        Gene:
                                        ZNF185 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        HGVS:
                                        NC_000023.11:g.152972965G>A, NW_003871103.3:g.406948G>A, NG_021255.2:g.63524G>A, NM_007150.3:c.*1692G>A, NM_001178108.2:c.*1692G>A, NM_001178108.1:c.*1692G>A, NM_001388432.2:c.*1692G>A, NM_001388432.1:c.*1692G>A, NM_001178113.2:c.*1692G>A, NM_001178113.1:c.*1692G>A, NM_001178115.2:c.*1692G>A, NM_001178115.1:c.*1692G>A, NM_001178106.1:c.*1692G>A, NM_001395254.1:c.*1692G>A, NM_001178107.1:c.*1692G>A, NM_001178109.1:c.*1692G>A, NM_001178110.1:c.*1692G>A, NW_025791818.1:g.588155G>A, NC_000023.10:g.152141509G>A, XM_005274746.4:c.*1692G>A, XM_005274746.3:c.*1692G>A, XM_005274746.2:c.*1692G>A, XM_005274746.1:c.*1692G>A, XM_017029822.3:c.*1692G>A, XM_017029822.2:c.*1692G>A, XM_017029822.1:c.*1692G>A, XM_005274738.3:c.*1692G>A, XM_005274738.2:c.*1692G>A, XM_005274738.1:c.*1692G>A, XM_005274741.3:c.*1692G>A, XM_005274741.2:c.*1692G>A, XM_005274741.1:c.*1692G>A, XM_005274740.3:c.*1692G>A, XM_005274740.2:c.*1692G>A, XM_005274740.1:c.*1692G>A, XM_005274742.3:c.*1692G>A, XM_005274742.2:c.*1692G>A, XM_005274742.1:c.*1692G>A, XM_005274744.3:c.*1692G>A, XM_005274744.2:c.*1692G>A, XM_005274744.1:c.*1692G>A, XM_005274745.3:c.*1692G>A, XM_005274745.2:c.*1692G>A, XM_005274745.1:c.*1692G>A, XM_017029821.2:c.*1692G>A, XM_017029821.1:c.*1692G>A, XM_017029823.2:c.*1692G>A, XM_017029823.1:c.*1692G>A, XM_017029824.2:c.*1692G>A, XM_017029824.1:c.*1692G>A, XM_017029825.2:c.*1692G>A, XM_017029825.1:c.*1692G>A, XM_017029826.2:c.*1692G>A, XM_017029826.1:c.*1692G>A, XM_017029827.2:c.*1692G>A, XM_017029827.1:c.*1692G>A, XM_017029828.2:c.*1692G>A, XM_017029828.1:c.*1692G>A, XM_017029829.2:c.*1692G>A, XM_017029829.1:c.*1692G>A, XM_017029830.2:c.*1692G>A, XM_017029830.1:c.*1692G>A, XM_017029831.2:c.*1692G>A, XM_017029831.1:c.*1692G>A, XM_017029832.2:c.*1692G>A, XM_017029832.1:c.*1692G>A, XM_017029833.2:c.*1692G>A, XM_017029833.1:c.*1692G>A, XM_017029834.2:c.*1692G>A, XM_017029834.1:c.*1692G>A, XM_017029835.2:c.*1692G>A, XM_017029835.1:c.*1692G>A, XM_011531194.2:c.*1692G>A, XM_011531194.1:c.*1692G>A, XM_011531195.2:c.*1692G>A, XM_011531195.1:c.*1692G>A, XM_047442488.1:c.*1692G>A, XM_047442489.1:c.*1692G>A, XM_047442490.1:c.*1692G>A, XM_047442491.1:c.*1692G>A, XM_047442496.1:c.*1692G>A, XM_047442492.1:c.*1692G>A, XM_047442493.1:c.*1692G>A, XM_047442494.1:c.*1692G>A, XM_047442495.1:c.*1692G>A, XM_047442497.1:c.*1692G>A, XM_047442498.1:c.*1692G>A, XM_047442499.1:c.*1692G>A, XM_047442500.1:c.*1692G>A, XM_047442501.1:c.*1692G>A, XM_047442502.1:c.*1692G>A, XM_047442503.1:c.*1692G>A, XM_047442505.1:c.*1692G>A, XM_047442507.1:c.*1692G>A, XM_047442508.1:c.*1692G>A, XM_047442509.1:c.*1692G>A, NM_001178114.1:c.*1692G>A, XM_047442506.1:c.*1692G>A, XM_047442504.1:c.*1692G>A

                                        20.

                                        rs1469443699 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>C [Show Flanks]
                                          Chromosome:
                                          X:152972657 (GRCh38)
                                          X:152141201 (GRCh37)
                                          Canonical SPDI:
                                          NC_000023.11:152972656:G:C
                                          Gene:
                                          ZNF185 (Varview)
                                          Functional Consequence:
                                          3_prime_UTR_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000008/2 (TOPMED)
                                          HGVS:
                                          NC_000023.11:g.152972657G>C, NW_003871103.3:g.406640G>C, NG_021255.2:g.63216G>C, NM_007150.3:c.*1384G>C, NM_001178108.2:c.*1384G>C, NM_001178108.1:c.*1384G>C, NM_001388432.2:c.*1384G>C, NM_001388432.1:c.*1384G>C, NM_001178113.2:c.*1384G>C, NM_001178113.1:c.*1384G>C, NM_001178115.2:c.*1384G>C, NM_001178115.1:c.*1384G>C, NM_001178106.1:c.*1384G>C, NM_001395254.1:c.*1384G>C, NM_001178107.1:c.*1384G>C, NM_001178109.1:c.*1384G>C, NM_001178110.1:c.*1384G>C, NW_025791818.1:g.587847G>C, NC_000023.10:g.152141201G>C, XM_005274746.4:c.*1384G>C, XM_005274746.3:c.*1384G>C, XM_005274746.2:c.*1384G>C, XM_005274746.1:c.*1384G>C, XM_017029822.3:c.*1384G>C, XM_017029822.2:c.*1384G>C, XM_017029822.1:c.*1384G>C, XM_005274738.3:c.*1384G>C, XM_005274738.2:c.*1384G>C, XM_005274738.1:c.*1384G>C, XM_005274741.3:c.*1384G>C, XM_005274741.2:c.*1384G>C, XM_005274741.1:c.*1384G>C, XM_005274740.3:c.*1384G>C, XM_005274740.2:c.*1384G>C, XM_005274740.1:c.*1384G>C, XM_005274742.3:c.*1384G>C, XM_005274742.2:c.*1384G>C, XM_005274742.1:c.*1384G>C, XM_005274744.3:c.*1384G>C, XM_005274744.2:c.*1384G>C, XM_005274744.1:c.*1384G>C, XM_005274745.3:c.*1384G>C, XM_005274745.2:c.*1384G>C, XM_005274745.1:c.*1384G>C, XM_017029821.2:c.*1384G>C, XM_017029821.1:c.*1384G>C, XM_017029823.2:c.*1384G>C, XM_017029823.1:c.*1384G>C, XM_017029824.2:c.*1384G>C, XM_017029824.1:c.*1384G>C, XM_017029825.2:c.*1384G>C, XM_017029825.1:c.*1384G>C, XM_017029826.2:c.*1384G>C, XM_017029826.1:c.*1384G>C, XM_017029827.2:c.*1384G>C, XM_017029827.1:c.*1384G>C, XM_017029828.2:c.*1384G>C, XM_017029828.1:c.*1384G>C, XM_017029829.2:c.*1384G>C, XM_017029829.1:c.*1384G>C, XM_017029830.2:c.*1384G>C, XM_017029830.1:c.*1384G>C, XM_017029831.2:c.*1384G>C, XM_017029831.1:c.*1384G>C, XM_017029832.2:c.*1384G>C, XM_017029832.1:c.*1384G>C, XM_017029833.2:c.*1384G>C, XM_017029833.1:c.*1384G>C, XM_017029834.2:c.*1384G>C, XM_017029834.1:c.*1384G>C, XM_017029835.2:c.*1384G>C, XM_017029835.1:c.*1384G>C, XM_011531194.2:c.*1384G>C, XM_011531194.1:c.*1384G>C, XM_011531195.2:c.*1384G>C, XM_011531195.1:c.*1384G>C, XM_047442488.1:c.*1384G>C, XM_047442489.1:c.*1384G>C, XM_047442490.1:c.*1384G>C, XM_047442491.1:c.*1384G>C, XM_047442496.1:c.*1384G>C, XM_047442492.1:c.*1384G>C, XM_047442493.1:c.*1384G>C, XM_047442494.1:c.*1384G>C, XM_047442495.1:c.*1384G>C, XM_047442497.1:c.*1384G>C, XM_047442498.1:c.*1384G>C, XM_047442499.1:c.*1384G>C, XM_047442500.1:c.*1384G>C, XM_047442501.1:c.*1384G>C, XM_047442502.1:c.*1384G>C, XM_047442503.1:c.*1384G>C, XM_047442505.1:c.*1384G>C, XM_047442507.1:c.*1384G>C, XM_047442508.1:c.*1384G>C, XM_047442509.1:c.*1384G>C, NM_001178114.1:c.*1384G>C, XM_047442506.1:c.*1384G>C, XM_047442504.1:c.*1384G>C

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...