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Items: 1 to 20 of 533

1.

rs1488747770 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    10:38118730 (GRCh38)
    10:38407658 (GRCh37)
    Canonical SPDI:
    NC_000010.11:38118729:G:A
    Gene:
    ZNF37A (Varview)
    Functional Consequence:
    3_prime_UTR_variant,missense_variant,coding_sequence_variant,intron_variant,genic_downstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    A=0.000111/1 (ALFA)
    A=0.000004/1 (GnomAD_exomes)
    HGVS:
    NC_000010.11:g.38118730G>A, NC_000010.10:g.38407658G>A, XM_005252586.5:c.1309G>A, XM_005252586.4:c.1309G>A, XM_005252586.3:c.1309G>A, XM_005252586.2:c.1309G>A, XM_005252586.1:c.1309G>A, NM_001007094.4:c.1579G>A, NM_001007094.3:c.1579G>A, NM_001007094.2:c.1579G>A, NM_003421.4:c.1579G>A, NM_003421.3:c.1579G>A, NM_003421.2:c.1579G>A, XM_011519658.4:c.1579G>A, XM_011519658.3:c.1579G>A, XM_011519658.2:c.1579G>A, XM_011519658.1:c.1579G>A, NM_001324259.3:c.*1335G>A, NM_001324259.2:c.*1335G>A, NM_001324259.1:c.*1335G>A, NM_001324246.3:c.1579G>A, NM_001324246.2:c.1579G>A, NM_001324246.1:c.1579G>A, XM_011519656.3:c.1579G>A, XM_011519656.2:c.1579G>A, XM_011519656.1:c.1579G>A, NM_001324251.3:c.1579G>A, NM_001324251.2:c.1579G>A, NM_001324251.1:c.1579G>A, NM_001324250.3:c.1579G>A, NM_001324250.2:c.1579G>A, NM_001324250.1:c.1579G>A, XM_011519657.3:c.1579G>A, XM_011519657.2:c.1579G>A, XM_011519657.1:c.1579G>A, NM_001324247.3:c.1579G>A, NM_001324247.2:c.1579G>A, NM_001324247.1:c.1579G>A, NM_001324248.3:c.1579G>A, NM_001324248.2:c.1579G>A, NM_001324248.1:c.1579G>A, NM_001324249.3:c.1579G>A, NM_001324249.2:c.1579G>A, NM_001324249.1:c.1579G>A, NM_001324260.3:c.*1335G>A, NM_001324260.2:c.*1335G>A, NM_001324260.1:c.*1335G>A, NM_001178101.3:c.1579G>A, NM_001178101.2:c.1579G>A, NM_001178101.1:c.1579G>A, NM_001324245.3:c.1579G>A, NM_001324245.2:c.1579G>A, NM_001324245.1:c.1579G>A, XM_047425722.1:c.1579G>A, XP_005252643.1:p.Val437Ile, NP_001007095.1:p.Val527Ile, NP_003412.1:p.Val527Ile, XP_011517960.1:p.Val527Ile, NP_001311175.1:p.Val527Ile, XP_011517958.1:p.Val527Ile, NP_001311180.1:p.Val527Ile, NP_001311179.1:p.Val527Ile, XP_011517959.1:p.Val527Ile, NP_001311176.1:p.Val527Ile, NP_001311177.1:p.Val527Ile, NP_001311178.1:p.Val527Ile, NP_001171572.1:p.Val527Ile, NP_001311174.1:p.Val527Ile, XP_047281678.1:p.Val527Ile

    2.

    rs1485917467 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G [Show Flanks]
      Chromosome:
      10:38118659 (GRCh38)
      10:38407587 (GRCh37)
      Canonical SPDI:
      NC_000010.11:38118658:C:G
      Gene:
      ZNF37A (Varview)
      Functional Consequence:
      3_prime_UTR_variant,intron_variant,stop_gained,genic_downstream_transcript_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      G=0./0 (ALFA)
      HGVS:
      NC_000010.11:g.38118659C>G, NC_000010.10:g.38407587C>G, XM_005252586.5:c.1238C>G, XM_005252586.4:c.1238C>G, XM_005252586.3:c.1238C>G, XM_005252586.2:c.1238C>G, XM_005252586.1:c.1238C>G, NM_001007094.4:c.1508C>G, NM_001007094.3:c.1508C>G, NM_001007094.2:c.1508C>G, NM_003421.4:c.1508C>G, NM_003421.3:c.1508C>G, NM_003421.2:c.1508C>G, XM_011519658.4:c.1508C>G, XM_011519658.3:c.1508C>G, XM_011519658.2:c.1508C>G, XM_011519658.1:c.1508C>G, NM_001324259.3:c.*1264C>G, NM_001324259.2:c.*1264C>G, NM_001324259.1:c.*1264C>G, NM_001324246.3:c.1508C>G, NM_001324246.2:c.1508C>G, NM_001324246.1:c.1508C>G, XM_011519656.3:c.1508C>G, XM_011519656.2:c.1508C>G, XM_011519656.1:c.1508C>G, NM_001324251.3:c.1508C>G, NM_001324251.2:c.1508C>G, NM_001324251.1:c.1508C>G, NM_001324250.3:c.1508C>G, NM_001324250.2:c.1508C>G, NM_001324250.1:c.1508C>G, XM_011519657.3:c.1508C>G, XM_011519657.2:c.1508C>G, XM_011519657.1:c.1508C>G, NM_001324247.3:c.1508C>G, NM_001324247.2:c.1508C>G, NM_001324247.1:c.1508C>G, NM_001324248.3:c.1508C>G, NM_001324248.2:c.1508C>G, NM_001324248.1:c.1508C>G, NM_001324249.3:c.1508C>G, NM_001324249.2:c.1508C>G, NM_001324249.1:c.1508C>G, NM_001324260.3:c.*1264C>G, NM_001324260.2:c.*1264C>G, NM_001324260.1:c.*1264C>G, NM_001178101.3:c.1508C>G, NM_001178101.2:c.1508C>G, NM_001178101.1:c.1508C>G, NM_001324245.3:c.1508C>G, NM_001324245.2:c.1508C>G, NM_001324245.1:c.1508C>G, XM_047425722.1:c.1508C>G, XP_005252643.1:p.Ser413Ter, NP_001007095.1:p.Ser503Ter, NP_003412.1:p.Ser503Ter, XP_011517960.1:p.Ser503Ter, NP_001311175.1:p.Ser503Ter, XP_011517958.1:p.Ser503Ter, NP_001311180.1:p.Ser503Ter, NP_001311179.1:p.Ser503Ter, XP_011517959.1:p.Ser503Ter, NP_001311176.1:p.Ser503Ter, NP_001311177.1:p.Ser503Ter, NP_001311178.1:p.Ser503Ter, NP_001171572.1:p.Ser503Ter, NP_001311174.1:p.Ser503Ter, XP_047281678.1:p.Ser503Ter

      3.

      rs1481987674 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        10:38118171 (GRCh38)
        10:38407099 (GRCh37)
        Canonical SPDI:
        NC_000010.11:38118170:A:G
        Gene:
        ZNF37A (Varview)
        Functional Consequence:
        3_prime_UTR_variant,intron_variant,synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa
        MAF:
        G=0.000047/1 (ALFA)
        G=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000010.11:g.38118171A>G, NC_000010.10:g.38407099A>G, XM_005252586.5:c.750A>G, XM_005252586.4:c.750A>G, XM_005252586.3:c.750A>G, XM_005252586.2:c.750A>G, XM_005252586.1:c.750A>G, NM_001007094.4:c.1020A>G, NM_001007094.3:c.1020A>G, NM_001007094.2:c.1020A>G, NM_003421.4:c.1020A>G, NM_003421.3:c.1020A>G, NM_003421.2:c.1020A>G, XM_011519658.4:c.1020A>G, XM_011519658.3:c.1020A>G, XM_011519658.2:c.1020A>G, XM_011519658.1:c.1020A>G, NM_001324259.3:c.*776A>G, NM_001324259.2:c.*776A>G, NM_001324259.1:c.*776A>G, NM_001324246.3:c.1020A>G, NM_001324246.2:c.1020A>G, NM_001324246.1:c.1020A>G, XM_011519656.3:c.1020A>G, XM_011519656.2:c.1020A>G, XM_011519656.1:c.1020A>G, NM_001324251.3:c.1020A>G, NM_001324251.2:c.1020A>G, NM_001324251.1:c.1020A>G, NM_001324250.3:c.1020A>G, NM_001324250.2:c.1020A>G, NM_001324250.1:c.1020A>G, XM_011519657.3:c.1020A>G, XM_011519657.2:c.1020A>G, XM_011519657.1:c.1020A>G, NM_001324247.3:c.1020A>G, NM_001324247.2:c.1020A>G, NM_001324247.1:c.1020A>G, NM_001324248.3:c.1020A>G, NM_001324248.2:c.1020A>G, NM_001324248.1:c.1020A>G, NM_001324249.3:c.1020A>G, NM_001324249.2:c.1020A>G, NM_001324249.1:c.1020A>G, NM_001324260.3:c.*776A>G, NM_001324260.2:c.*776A>G, NM_001324260.1:c.*776A>G, NM_001178101.3:c.1020A>G, NM_001178101.2:c.1020A>G, NM_001178101.1:c.1020A>G, NM_001324245.3:c.1020A>G, NM_001324245.2:c.1020A>G, NM_001324245.1:c.1020A>G, XM_047425722.1:c.1020A>G

        4.

        rs1478877450 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>C [Show Flanks]
          Chromosome:
          10:38117739 (GRCh38)
          10:38406667 (GRCh37)
          Canonical SPDI:
          NC_000010.11:38117738:A:C
          Gene:
          ZNF37A (Varview)
          Functional Consequence:
          3_prime_UTR_variant,intron_variant,synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
          Validated:
          by frequency
          MAF:
          C=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000010.11:g.38117739A>C, NC_000010.10:g.38406667A>C, XM_005252586.5:c.318A>C, XM_005252586.4:c.318A>C, XM_005252586.3:c.318A>C, XM_005252586.2:c.318A>C, XM_005252586.1:c.318A>C, NM_001007094.4:c.588A>C, NM_001007094.3:c.588A>C, NM_001007094.2:c.588A>C, NM_003421.4:c.588A>C, NM_003421.3:c.588A>C, NM_003421.2:c.588A>C, XM_011519658.4:c.588A>C, XM_011519658.3:c.588A>C, XM_011519658.2:c.588A>C, XM_011519658.1:c.588A>C, NM_001324259.3:c.*344A>C, NM_001324259.2:c.*344A>C, NM_001324259.1:c.*344A>C, NM_001324246.3:c.588A>C, NM_001324246.2:c.588A>C, NM_001324246.1:c.588A>C, XM_011519656.3:c.588A>C, XM_011519656.2:c.588A>C, XM_011519656.1:c.588A>C, NM_001324251.3:c.588A>C, NM_001324251.2:c.588A>C, NM_001324251.1:c.588A>C, NM_001324250.3:c.588A>C, NM_001324250.2:c.588A>C, NM_001324250.1:c.588A>C, XM_011519657.3:c.588A>C, XM_011519657.2:c.588A>C, XM_011519657.1:c.588A>C, NM_001324247.3:c.588A>C, NM_001324247.2:c.588A>C, NM_001324247.1:c.588A>C, NM_001324248.3:c.588A>C, NM_001324248.2:c.588A>C, NM_001324248.1:c.588A>C, NM_001324249.3:c.588A>C, NM_001324249.2:c.588A>C, NM_001324249.1:c.588A>C, NM_001324260.3:c.*344A>C, NM_001324260.2:c.*344A>C, NM_001324260.1:c.*344A>C, NM_001178101.3:c.588A>C, NM_001178101.2:c.588A>C, NM_001178101.1:c.588A>C, NM_001324245.3:c.588A>C, NM_001324245.2:c.588A>C, NM_001324245.1:c.588A>C, XM_047425722.1:c.588A>C

          5.

          rs1477101464 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            10:38117546 (GRCh38)
            10:38406474 (GRCh37)
            Canonical SPDI:
            NC_000010.11:38117545:A:G
            Gene:
            ZNF37A (Varview)
            Functional Consequence:
            3_prime_UTR_variant,intron_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
            Validated:
            by frequency,by alfa
            MAF:
            G=0.000071/1 (ALFA)
            G=0.000008/2 (TOPMED)
            HGVS:
            NC_000010.11:g.38117546A>G, NC_000010.10:g.38406474A>G, XM_005252586.5:c.125A>G, XM_005252586.4:c.125A>G, XM_005252586.3:c.125A>G, XM_005252586.2:c.125A>G, XM_005252586.1:c.125A>G, NM_001007094.4:c.395A>G, NM_001007094.3:c.395A>G, NM_001007094.2:c.395A>G, NM_003421.4:c.395A>G, NM_003421.3:c.395A>G, NM_003421.2:c.395A>G, XM_011519658.4:c.395A>G, XM_011519658.3:c.395A>G, XM_011519658.2:c.395A>G, XM_011519658.1:c.395A>G, NM_001324259.3:c.*151A>G, NM_001324259.2:c.*151A>G, NM_001324259.1:c.*151A>G, NM_001324246.3:c.395A>G, NM_001324246.2:c.395A>G, NM_001324246.1:c.395A>G, XM_011519656.3:c.395A>G, XM_011519656.2:c.395A>G, XM_011519656.1:c.395A>G, NM_001324251.3:c.395A>G, NM_001324251.2:c.395A>G, NM_001324251.1:c.395A>G, NM_001324250.3:c.395A>G, NM_001324250.2:c.395A>G, NM_001324250.1:c.395A>G, XM_011519657.3:c.395A>G, XM_011519657.2:c.395A>G, XM_011519657.1:c.395A>G, NM_001324247.3:c.395A>G, NM_001324247.2:c.395A>G, NM_001324247.1:c.395A>G, NM_001324248.3:c.395A>G, NM_001324248.2:c.395A>G, NM_001324248.1:c.395A>G, NM_001324249.3:c.395A>G, NM_001324249.2:c.395A>G, NM_001324249.1:c.395A>G, NM_001324260.3:c.*151A>G, NM_001324260.2:c.*151A>G, NM_001324260.1:c.*151A>G, NM_001178101.3:c.395A>G, NM_001178101.2:c.395A>G, NM_001178101.1:c.395A>G, NM_001324245.3:c.395A>G, NM_001324245.2:c.395A>G, NM_001324245.1:c.395A>G, XM_047425722.1:c.395A>G, XP_005252643.1:p.Asp42Gly, NP_001007095.1:p.Asp132Gly, NP_003412.1:p.Asp132Gly, XP_011517960.1:p.Asp132Gly, NP_001311175.1:p.Asp132Gly, XP_011517958.1:p.Asp132Gly, NP_001311180.1:p.Asp132Gly, NP_001311179.1:p.Asp132Gly, XP_011517959.1:p.Asp132Gly, NP_001311176.1:p.Asp132Gly, NP_001311177.1:p.Asp132Gly, NP_001311178.1:p.Asp132Gly, NP_001171572.1:p.Asp132Gly, NP_001311174.1:p.Asp132Gly, XP_047281678.1:p.Asp132Gly

            6.

            rs1474633815 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              10:38118731 (GRCh38)
              10:38407659 (GRCh37)
              Canonical SPDI:
              NC_000010.11:38118730:T:C
              Gene:
              ZNF37A (Varview)
              Functional Consequence:
              3_prime_UTR_variant,intron_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa
              MAF:
              C=0./0 (ALFA)
              C=0.000004/1 (TOPMED)
              HGVS:
              NC_000010.11:g.38118731T>C, NC_000010.10:g.38407659T>C, XM_005252586.5:c.1310T>C, XM_005252586.4:c.1310T>C, XM_005252586.3:c.1310T>C, XM_005252586.2:c.1310T>C, XM_005252586.1:c.1310T>C, NM_001007094.4:c.1580T>C, NM_001007094.3:c.1580T>C, NM_001007094.2:c.1580T>C, NM_003421.4:c.1580T>C, NM_003421.3:c.1580T>C, NM_003421.2:c.1580T>C, XM_011519658.4:c.1580T>C, XM_011519658.3:c.1580T>C, XM_011519658.2:c.1580T>C, XM_011519658.1:c.1580T>C, NM_001324259.3:c.*1336T>C, NM_001324259.2:c.*1336T>C, NM_001324259.1:c.*1336T>C, NM_001324246.3:c.1580T>C, NM_001324246.2:c.1580T>C, NM_001324246.1:c.1580T>C, XM_011519656.3:c.1580T>C, XM_011519656.2:c.1580T>C, XM_011519656.1:c.1580T>C, NM_001324251.3:c.1580T>C, NM_001324251.2:c.1580T>C, NM_001324251.1:c.1580T>C, NM_001324250.3:c.1580T>C, NM_001324250.2:c.1580T>C, NM_001324250.1:c.1580T>C, XM_011519657.3:c.1580T>C, XM_011519657.2:c.1580T>C, XM_011519657.1:c.1580T>C, NM_001324247.3:c.1580T>C, NM_001324247.2:c.1580T>C, NM_001324247.1:c.1580T>C, NM_001324248.3:c.1580T>C, NM_001324248.2:c.1580T>C, NM_001324248.1:c.1580T>C, NM_001324249.3:c.1580T>C, NM_001324249.2:c.1580T>C, NM_001324249.1:c.1580T>C, NM_001324260.3:c.*1336T>C, NM_001324260.2:c.*1336T>C, NM_001324260.1:c.*1336T>C, NM_001178101.3:c.1580T>C, NM_001178101.2:c.1580T>C, NM_001178101.1:c.1580T>C, NM_001324245.3:c.1580T>C, NM_001324245.2:c.1580T>C, NM_001324245.1:c.1580T>C, XM_047425722.1:c.1580T>C, XP_005252643.1:p.Val437Ala, NP_001007095.1:p.Val527Ala, NP_003412.1:p.Val527Ala, XP_011517960.1:p.Val527Ala, NP_001311175.1:p.Val527Ala, XP_011517958.1:p.Val527Ala, NP_001311180.1:p.Val527Ala, NP_001311179.1:p.Val527Ala, XP_011517959.1:p.Val527Ala, NP_001311176.1:p.Val527Ala, NP_001311177.1:p.Val527Ala, NP_001311178.1:p.Val527Ala, NP_001171572.1:p.Val527Ala, NP_001311174.1:p.Val527Ala, XP_047281678.1:p.Val527Ala

              7.

              rs1474627319 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>T [Show Flanks]
                Chromosome:
                10:38118107 (GRCh38)
                10:38407035 (GRCh37)
                Canonical SPDI:
                NC_000010.11:38118106:G:T
                Gene:
                ZNF37A (Varview)
                Functional Consequence:
                3_prime_UTR_variant,intron_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0.000056/2 (ALFA)
                T=0.000012/3 (GnomAD_exomes)
                T=0.000014/2 (GnomAD)
                T=0.000019/5 (TOPMED)
                HGVS:
                NC_000010.11:g.38118107G>T, NC_000010.10:g.38407035G>T, XM_005252586.5:c.686G>T, XM_005252586.4:c.686G>T, XM_005252586.3:c.686G>T, XM_005252586.2:c.686G>T, XM_005252586.1:c.686G>T, NM_001007094.4:c.956G>T, NM_001007094.3:c.956G>T, NM_001007094.2:c.956G>T, NM_003421.4:c.956G>T, NM_003421.3:c.956G>T, NM_003421.2:c.956G>T, XM_011519658.4:c.956G>T, XM_011519658.3:c.956G>T, XM_011519658.2:c.956G>T, XM_011519658.1:c.956G>T, NM_001324259.3:c.*712G>T, NM_001324259.2:c.*712G>T, NM_001324259.1:c.*712G>T, NM_001324246.3:c.956G>T, NM_001324246.2:c.956G>T, NM_001324246.1:c.956G>T, XM_011519656.3:c.956G>T, XM_011519656.2:c.956G>T, XM_011519656.1:c.956G>T, NM_001324251.3:c.956G>T, NM_001324251.2:c.956G>T, NM_001324251.1:c.956G>T, NM_001324250.3:c.956G>T, NM_001324250.2:c.956G>T, NM_001324250.1:c.956G>T, XM_011519657.3:c.956G>T, XM_011519657.2:c.956G>T, XM_011519657.1:c.956G>T, NM_001324247.3:c.956G>T, NM_001324247.2:c.956G>T, NM_001324247.1:c.956G>T, NM_001324248.3:c.956G>T, NM_001324248.2:c.956G>T, NM_001324248.1:c.956G>T, NM_001324249.3:c.956G>T, NM_001324249.2:c.956G>T, NM_001324249.1:c.956G>T, NM_001324260.3:c.*712G>T, NM_001324260.2:c.*712G>T, NM_001324260.1:c.*712G>T, NM_001178101.3:c.956G>T, NM_001178101.2:c.956G>T, NM_001178101.1:c.956G>T, NM_001324245.3:c.956G>T, NM_001324245.2:c.956G>T, NM_001324245.1:c.956G>T, XM_047425722.1:c.956G>T, XP_005252643.1:p.Arg229Ile, NP_001007095.1:p.Arg319Ile, NP_003412.1:p.Arg319Ile, XP_011517960.1:p.Arg319Ile, NP_001311175.1:p.Arg319Ile, XP_011517958.1:p.Arg319Ile, NP_001311180.1:p.Arg319Ile, NP_001311179.1:p.Arg319Ile, XP_011517959.1:p.Arg319Ile, NP_001311176.1:p.Arg319Ile, NP_001311177.1:p.Arg319Ile, NP_001311178.1:p.Arg319Ile, NP_001171572.1:p.Arg319Ile, NP_001311174.1:p.Arg319Ile, XP_047281678.1:p.Arg319Ile

                8.

                rs1471455663 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>T [Show Flanks]
                  Chromosome:
                  10:38118088 (GRCh38)
                  10:38407016 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:38118087:G:T
                  Gene:
                  ZNF37A (Varview)
                  Functional Consequence:
                  coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,missense_variant,intron_variant
                  Validated:
                  by frequency
                  MAF:
                  T=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000010.11:g.38118088G>T, NC_000010.10:g.38407016G>T, XM_005252586.5:c.667G>T, XM_005252586.4:c.667G>T, XM_005252586.3:c.667G>T, XM_005252586.2:c.667G>T, XM_005252586.1:c.667G>T, NM_001007094.4:c.937G>T, NM_001007094.3:c.937G>T, NM_001007094.2:c.937G>T, NM_003421.4:c.937G>T, NM_003421.3:c.937G>T, NM_003421.2:c.937G>T, XM_011519658.4:c.937G>T, XM_011519658.3:c.937G>T, XM_011519658.2:c.937G>T, XM_011519658.1:c.937G>T, NM_001324259.3:c.*693G>T, NM_001324259.2:c.*693G>T, NM_001324259.1:c.*693G>T, NM_001324246.3:c.937G>T, NM_001324246.2:c.937G>T, NM_001324246.1:c.937G>T, XM_011519656.3:c.937G>T, XM_011519656.2:c.937G>T, XM_011519656.1:c.937G>T, NM_001324251.3:c.937G>T, NM_001324251.2:c.937G>T, NM_001324251.1:c.937G>T, NM_001324250.3:c.937G>T, NM_001324250.2:c.937G>T, NM_001324250.1:c.937G>T, XM_011519657.3:c.937G>T, XM_011519657.2:c.937G>T, XM_011519657.1:c.937G>T, NM_001324247.3:c.937G>T, NM_001324247.2:c.937G>T, NM_001324247.1:c.937G>T, NM_001324248.3:c.937G>T, NM_001324248.2:c.937G>T, NM_001324248.1:c.937G>T, NM_001324249.3:c.937G>T, NM_001324249.2:c.937G>T, NM_001324249.1:c.937G>T, NM_001324260.3:c.*693G>T, NM_001324260.2:c.*693G>T, NM_001324260.1:c.*693G>T, NM_001178101.3:c.937G>T, NM_001178101.2:c.937G>T, NM_001178101.1:c.937G>T, NM_001324245.3:c.937G>T, NM_001324245.2:c.937G>T, NM_001324245.1:c.937G>T, XM_047425722.1:c.937G>T, XP_005252643.1:p.Asp223Tyr, NP_001007095.1:p.Asp313Tyr, NP_003412.1:p.Asp313Tyr, XP_011517960.1:p.Asp313Tyr, NP_001311175.1:p.Asp313Tyr, XP_011517958.1:p.Asp313Tyr, NP_001311180.1:p.Asp313Tyr, NP_001311179.1:p.Asp313Tyr, XP_011517959.1:p.Asp313Tyr, NP_001311176.1:p.Asp313Tyr, NP_001311177.1:p.Asp313Tyr, NP_001311178.1:p.Asp313Tyr, NP_001171572.1:p.Asp313Tyr, NP_001311174.1:p.Asp313Tyr, XP_047281678.1:p.Asp313Tyr

                  9.

                  rs1471354393 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    10:38118763 (GRCh38)
                    10:38407691 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:38118762:C:T
                    Gene:
                    ZNF37A (Varview)
                    Functional Consequence:
                    synonymous_variant,coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000010.11:g.38118763C>T, NC_000010.10:g.38407691C>T, XM_005252586.5:c.1342C>T, XM_005252586.4:c.1342C>T, XM_005252586.3:c.1342C>T, XM_005252586.2:c.1342C>T, XM_005252586.1:c.1342C>T, NM_001007094.4:c.1612C>T, NM_001007094.3:c.1612C>T, NM_001007094.2:c.1612C>T, NM_003421.4:c.1612C>T, NM_003421.3:c.1612C>T, NM_003421.2:c.1612C>T, XM_011519658.4:c.1612C>T, XM_011519658.3:c.1612C>T, XM_011519658.2:c.1612C>T, XM_011519658.1:c.1612C>T, NM_001324259.3:c.*1368C>T, NM_001324259.2:c.*1368C>T, NM_001324259.1:c.*1368C>T, NM_001324246.3:c.1612C>T, NM_001324246.2:c.1612C>T, NM_001324246.1:c.1612C>T, XM_011519656.3:c.1612C>T, XM_011519656.2:c.1612C>T, XM_011519656.1:c.1612C>T, NM_001324251.3:c.1612C>T, NM_001324251.2:c.1612C>T, NM_001324251.1:c.1612C>T, NM_001324250.3:c.1612C>T, NM_001324250.2:c.1612C>T, NM_001324250.1:c.1612C>T, XM_011519657.3:c.1612C>T, XM_011519657.2:c.1612C>T, XM_011519657.1:c.1612C>T, NM_001324247.3:c.1612C>T, NM_001324247.2:c.1612C>T, NM_001324247.1:c.1612C>T, NM_001324248.3:c.1612C>T, NM_001324248.2:c.1612C>T, NM_001324248.1:c.1612C>T, NM_001324249.3:c.1612C>T, NM_001324249.2:c.1612C>T, NM_001324249.1:c.1612C>T, NM_001324260.3:c.*1368C>T, NM_001324260.2:c.*1368C>T, NM_001324260.1:c.*1368C>T, NM_001178101.3:c.1612C>T, NM_001178101.2:c.1612C>T, NM_001178101.1:c.1612C>T, NM_001324245.3:c.1612C>T, NM_001324245.2:c.1612C>T, NM_001324245.1:c.1612C>T, XM_047425722.1:c.1612C>T

                    10.

                    rs1470003498 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,T [Show Flanks]
                      Chromosome:
                      10:38117650 (GRCh38)
                      10:38406578 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:38117649:G:A,NC_000010.11:38117649:G:T
                      Gene:
                      ZNF37A (Varview)
                      Functional Consequence:
                      coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,missense_variant,intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      A=0.000004/1 (GnomAD_exomes)
                      T=0.000007/1 (GnomAD)
                      HGVS:
                      NC_000010.11:g.38117650G>A, NC_000010.11:g.38117650G>T, NC_000010.10:g.38406578G>A, NC_000010.10:g.38406578G>T, XM_005252586.5:c.229G>A, XM_005252586.5:c.229G>T, XM_005252586.4:c.229G>A, XM_005252586.4:c.229G>T, XM_005252586.3:c.229G>A, XM_005252586.3:c.229G>T, XM_005252586.2:c.229G>A, XM_005252586.2:c.229G>T, XM_005252586.1:c.229G>A, XM_005252586.1:c.229G>T, NM_001007094.4:c.499G>A, NM_001007094.4:c.499G>T, NM_001007094.3:c.499G>A, NM_001007094.3:c.499G>T, NM_001007094.2:c.499G>A, NM_001007094.2:c.499G>T, NM_003421.4:c.499G>A, NM_003421.4:c.499G>T, NM_003421.3:c.499G>A, NM_003421.3:c.499G>T, NM_003421.2:c.499G>A, NM_003421.2:c.499G>T, XM_011519658.4:c.499G>A, XM_011519658.4:c.499G>T, XM_011519658.3:c.499G>A, XM_011519658.3:c.499G>T, XM_011519658.2:c.499G>A, XM_011519658.2:c.499G>T, XM_011519658.1:c.499G>A, XM_011519658.1:c.499G>T, NM_001324259.3:c.*255G>A, NM_001324259.3:c.*255G>T, NM_001324259.2:c.*255G>A, NM_001324259.2:c.*255G>T, NM_001324259.1:c.*255G>A, NM_001324259.1:c.*255G>T, NM_001324246.3:c.499G>A, NM_001324246.3:c.499G>T, NM_001324246.2:c.499G>A, NM_001324246.2:c.499G>T, NM_001324246.1:c.499G>A, NM_001324246.1:c.499G>T, XM_011519656.3:c.499G>A, XM_011519656.3:c.499G>T, XM_011519656.2:c.499G>A, XM_011519656.2:c.499G>T, XM_011519656.1:c.499G>A, XM_011519656.1:c.499G>T, NM_001324251.3:c.499G>A, NM_001324251.3:c.499G>T, NM_001324251.2:c.499G>A, NM_001324251.2:c.499G>T, NM_001324251.1:c.499G>A, NM_001324251.1:c.499G>T, NM_001324250.3:c.499G>A, NM_001324250.3:c.499G>T, NM_001324250.2:c.499G>A, NM_001324250.2:c.499G>T, NM_001324250.1:c.499G>A, NM_001324250.1:c.499G>T, XM_011519657.3:c.499G>A, XM_011519657.3:c.499G>T, XM_011519657.2:c.499G>A, XM_011519657.2:c.499G>T, XM_011519657.1:c.499G>A, XM_011519657.1:c.499G>T, NM_001324247.3:c.499G>A, NM_001324247.3:c.499G>T, NM_001324247.2:c.499G>A, NM_001324247.2:c.499G>T, NM_001324247.1:c.499G>A, NM_001324247.1:c.499G>T, NM_001324248.3:c.499G>A, NM_001324248.3:c.499G>T, NM_001324248.2:c.499G>A, NM_001324248.2:c.499G>T, NM_001324248.1:c.499G>A, NM_001324248.1:c.499G>T, NM_001324249.3:c.499G>A, NM_001324249.3:c.499G>T, NM_001324249.2:c.499G>A, NM_001324249.2:c.499G>T, NM_001324249.1:c.499G>A, NM_001324249.1:c.499G>T, NM_001324260.3:c.*255G>A, NM_001324260.3:c.*255G>T, NM_001324260.2:c.*255G>A, NM_001324260.2:c.*255G>T, NM_001324260.1:c.*255G>A, NM_001324260.1:c.*255G>T, NM_001178101.3:c.499G>A, NM_001178101.3:c.499G>T, NM_001178101.2:c.499G>A, NM_001178101.2:c.499G>T, NM_001178101.1:c.499G>A, NM_001178101.1:c.499G>T, NM_001324245.3:c.499G>A, NM_001324245.3:c.499G>T, NM_001324245.2:c.499G>A, NM_001324245.2:c.499G>T, NM_001324245.1:c.499G>A, NM_001324245.1:c.499G>T, XM_047425722.1:c.499G>A, XM_047425722.1:c.499G>T, XP_005252643.1:p.Gly77Ser, XP_005252643.1:p.Gly77Cys, NP_001007095.1:p.Gly167Ser, NP_001007095.1:p.Gly167Cys, NP_003412.1:p.Gly167Ser, NP_003412.1:p.Gly167Cys, XP_011517960.1:p.Gly167Ser, XP_011517960.1:p.Gly167Cys, NP_001311175.1:p.Gly167Ser, NP_001311175.1:p.Gly167Cys, XP_011517958.1:p.Gly167Ser, XP_011517958.1:p.Gly167Cys, NP_001311180.1:p.Gly167Ser, NP_001311180.1:p.Gly167Cys, NP_001311179.1:p.Gly167Ser, NP_001311179.1:p.Gly167Cys, XP_011517959.1:p.Gly167Ser, XP_011517959.1:p.Gly167Cys, NP_001311176.1:p.Gly167Ser, NP_001311176.1:p.Gly167Cys, NP_001311177.1:p.Gly167Ser, NP_001311177.1:p.Gly167Cys, NP_001311178.1:p.Gly167Ser, NP_001311178.1:p.Gly167Cys, NP_001171572.1:p.Gly167Ser, NP_001171572.1:p.Gly167Cys, NP_001311174.1:p.Gly167Ser, NP_001311174.1:p.Gly167Cys, XP_047281678.1:p.Gly167Ser, XP_047281678.1:p.Gly167Cys

                      11.

                      rs1469376611 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>T [Show Flanks]
                        Chromosome:
                        10:38118305 (GRCh38)
                        10:38407233 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:38118304:G:T
                        Gene:
                        ZNF37A (Varview)
                        Functional Consequence:
                        coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,missense_variant,intron_variant
                        HGVS:
                        NC_000010.11:g.38118305G>T, NC_000010.10:g.38407233G>T, XM_005252586.5:c.884G>T, XM_005252586.4:c.884G>T, XM_005252586.3:c.884G>T, XM_005252586.2:c.884G>T, XM_005252586.1:c.884G>T, NM_001007094.4:c.1154G>T, NM_001007094.3:c.1154G>T, NM_001007094.2:c.1154G>T, NM_003421.4:c.1154G>T, NM_003421.3:c.1154G>T, NM_003421.2:c.1154G>T, XM_011519658.4:c.1154G>T, XM_011519658.3:c.1154G>T, XM_011519658.2:c.1154G>T, XM_011519658.1:c.1154G>T, NM_001324259.3:c.*910G>T, NM_001324259.2:c.*910G>T, NM_001324259.1:c.*910G>T, NM_001324246.3:c.1154G>T, NM_001324246.2:c.1154G>T, NM_001324246.1:c.1154G>T, XM_011519656.3:c.1154G>T, XM_011519656.2:c.1154G>T, XM_011519656.1:c.1154G>T, NM_001324251.3:c.1154G>T, NM_001324251.2:c.1154G>T, NM_001324251.1:c.1154G>T, NM_001324250.3:c.1154G>T, NM_001324250.2:c.1154G>T, NM_001324250.1:c.1154G>T, XM_011519657.3:c.1154G>T, XM_011519657.2:c.1154G>T, XM_011519657.1:c.1154G>T, NM_001324247.3:c.1154G>T, NM_001324247.2:c.1154G>T, NM_001324247.1:c.1154G>T, NM_001324248.3:c.1154G>T, NM_001324248.2:c.1154G>T, NM_001324248.1:c.1154G>T, NM_001324249.3:c.1154G>T, NM_001324249.2:c.1154G>T, NM_001324249.1:c.1154G>T, NM_001324260.3:c.*910G>T, NM_001324260.2:c.*910G>T, NM_001324260.1:c.*910G>T, NM_001178101.3:c.1154G>T, NM_001178101.2:c.1154G>T, NM_001178101.1:c.1154G>T, NM_001324245.3:c.1154G>T, NM_001324245.2:c.1154G>T, NM_001324245.1:c.1154G>T, XM_047425722.1:c.1154G>T, XP_005252643.1:p.Cys295Phe, NP_001007095.1:p.Cys385Phe, NP_003412.1:p.Cys385Phe, XP_011517960.1:p.Cys385Phe, NP_001311175.1:p.Cys385Phe, XP_011517958.1:p.Cys385Phe, NP_001311180.1:p.Cys385Phe, NP_001311179.1:p.Cys385Phe, XP_011517959.1:p.Cys385Phe, NP_001311176.1:p.Cys385Phe, NP_001311177.1:p.Cys385Phe, NP_001311178.1:p.Cys385Phe, NP_001171572.1:p.Cys385Phe, NP_001311174.1:p.Cys385Phe, XP_047281678.1:p.Cys385Phe

                        12.

                        rs1464552640 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C,T [Show Flanks]
                          Chromosome:
                          10:38118834 (GRCh38)
                          10:38407762 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:38118833:G:A,NC_000010.11:38118833:G:C,NC_000010.11:38118833:G:T
                          Gene:
                          ZNF37A (Varview)
                          Functional Consequence:
                          synonymous_variant,coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          HGVS:
                          NC_000010.11:g.38118834G>A, NC_000010.11:g.38118834G>C, NC_000010.11:g.38118834G>T, NC_000010.10:g.38407762G>A, NC_000010.10:g.38407762G>C, NC_000010.10:g.38407762G>T, XM_005252586.5:c.1413G>A, XM_005252586.5:c.1413G>C, XM_005252586.5:c.1413G>T, XM_005252586.4:c.1413G>A, XM_005252586.4:c.1413G>C, XM_005252586.4:c.1413G>T, XM_005252586.3:c.1413G>A, XM_005252586.3:c.1413G>C, XM_005252586.3:c.1413G>T, XM_005252586.2:c.1413G>A, XM_005252586.2:c.1413G>C, XM_005252586.2:c.1413G>T, XM_005252586.1:c.1413G>A, XM_005252586.1:c.1413G>C, XM_005252586.1:c.1413G>T, NM_001007094.4:c.1683G>A, NM_001007094.4:c.1683G>C, NM_001007094.4:c.1683G>T, NM_001007094.3:c.1683G>A, NM_001007094.3:c.1683G>C, NM_001007094.3:c.1683G>T, NM_001007094.2:c.1683G>A, NM_001007094.2:c.1683G>C, NM_001007094.2:c.1683G>T, NM_003421.4:c.1683G>A, NM_003421.4:c.1683G>C, NM_003421.4:c.1683G>T, NM_003421.3:c.1683G>A, NM_003421.3:c.1683G>C, NM_003421.3:c.1683G>T, NM_003421.2:c.1683G>A, NM_003421.2:c.1683G>C, NM_003421.2:c.1683G>T, XM_011519658.4:c.1683G>A, XM_011519658.4:c.1683G>C, XM_011519658.4:c.1683G>T, XM_011519658.3:c.1683G>A, XM_011519658.3:c.1683G>C, XM_011519658.3:c.1683G>T, XM_011519658.2:c.1683G>A, XM_011519658.2:c.1683G>C, XM_011519658.2:c.1683G>T, XM_011519658.1:c.1683G>A, XM_011519658.1:c.1683G>C, XM_011519658.1:c.1683G>T, NM_001324259.3:c.*1439G>A, NM_001324259.3:c.*1439G>C, NM_001324259.3:c.*1439G>T, NM_001324259.2:c.*1439G>A, NM_001324259.2:c.*1439G>C, NM_001324259.2:c.*1439G>T, NM_001324259.1:c.*1439G>A, NM_001324259.1:c.*1439G>C, NM_001324259.1:c.*1439G>T, NM_001324246.3:c.1683G>A, NM_001324246.3:c.1683G>C, NM_001324246.3:c.1683G>T, NM_001324246.2:c.1683G>A, NM_001324246.2:c.1683G>C, NM_001324246.2:c.1683G>T, NM_001324246.1:c.1683G>A, NM_001324246.1:c.1683G>C, NM_001324246.1:c.1683G>T, XM_011519656.3:c.1683G>A, XM_011519656.3:c.1683G>C, XM_011519656.3:c.1683G>T, XM_011519656.2:c.1683G>A, XM_011519656.2:c.1683G>C, XM_011519656.2:c.1683G>T, XM_011519656.1:c.1683G>A, XM_011519656.1:c.1683G>C, XM_011519656.1:c.1683G>T, NM_001324251.3:c.1683G>A, NM_001324251.3:c.1683G>C, NM_001324251.3:c.1683G>T, NM_001324251.2:c.1683G>A, NM_001324251.2:c.1683G>C, NM_001324251.2:c.1683G>T, NM_001324251.1:c.1683G>A, NM_001324251.1:c.1683G>C, NM_001324251.1:c.1683G>T, NM_001324250.3:c.1683G>A, NM_001324250.3:c.1683G>C, NM_001324250.3:c.1683G>T, NM_001324250.2:c.1683G>A, NM_001324250.2:c.1683G>C, NM_001324250.2:c.1683G>T, NM_001324250.1:c.1683G>A, NM_001324250.1:c.1683G>C, NM_001324250.1:c.1683G>T, XM_011519657.3:c.1683G>A, XM_011519657.3:c.1683G>C, XM_011519657.3:c.1683G>T, XM_011519657.2:c.1683G>A, XM_011519657.2:c.1683G>C, XM_011519657.2:c.1683G>T, XM_011519657.1:c.1683G>A, XM_011519657.1:c.1683G>C, XM_011519657.1:c.1683G>T, NM_001324247.3:c.1683G>A, NM_001324247.3:c.1683G>C, NM_001324247.3:c.1683G>T, NM_001324247.2:c.1683G>A, NM_001324247.2:c.1683G>C, NM_001324247.2:c.1683G>T, NM_001324247.1:c.1683G>A, NM_001324247.1:c.1683G>C, NM_001324247.1:c.1683G>T, NM_001324248.3:c.1683G>A, NM_001324248.3:c.1683G>C, NM_001324248.3:c.1683G>T, NM_001324248.2:c.1683G>A, NM_001324248.2:c.1683G>C, NM_001324248.2:c.1683G>T, NM_001324248.1:c.1683G>A, NM_001324248.1:c.1683G>C, NM_001324248.1:c.1683G>T, NM_001324249.3:c.1683G>A, NM_001324249.3:c.1683G>C, NM_001324249.3:c.1683G>T, NM_001324249.2:c.1683G>A, NM_001324249.2:c.1683G>C, NM_001324249.2:c.1683G>T, NM_001324249.1:c.1683G>A, NM_001324249.1:c.1683G>C, NM_001324249.1:c.1683G>T, NM_001324260.3:c.*1439G>A, NM_001324260.3:c.*1439G>C, NM_001324260.3:c.*1439G>T, NM_001324260.2:c.*1439G>A, NM_001324260.2:c.*1439G>C, NM_001324260.2:c.*1439G>T, NM_001324260.1:c.*1439G>A, NM_001324260.1:c.*1439G>C, NM_001324260.1:c.*1439G>T, NM_001178101.3:c.1683G>A, NM_001178101.3:c.1683G>C, NM_001178101.3:c.1683G>T, NM_001178101.2:c.1683G>A, NM_001178101.2:c.1683G>C, NM_001178101.2:c.1683G>T, NM_001178101.1:c.1683G>A, NM_001178101.1:c.1683G>C, NM_001178101.1:c.1683G>T, NM_001324245.3:c.1683G>A, NM_001324245.3:c.1683G>C, NM_001324245.3:c.1683G>T, NM_001324245.2:c.1683G>A, NM_001324245.2:c.1683G>C, NM_001324245.2:c.1683G>T, NM_001324245.1:c.1683G>A, NM_001324245.1:c.1683G>C, NM_001324245.1:c.1683G>T, XM_047425722.1:c.1683G>A, XM_047425722.1:c.1683G>C, XM_047425722.1:c.1683G>T

                          13.

                          rs1461967801 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G [Show Flanks]
                            Chromosome:
                            10:38118338 (GRCh38)
                            10:38407266 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:38118337:C:G
                            Gene:
                            ZNF37A (Varview)
                            Functional Consequence:
                            coding_sequence_variant,3_prime_UTR_variant,stop_gained,genic_downstream_transcript_variant,intron_variant
                            Validated:
                            by frequency
                            MAF:
                            G=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000010.11:g.38118338C>G, NC_000010.10:g.38407266C>G, XM_005252586.5:c.917C>G, XM_005252586.4:c.917C>G, XM_005252586.3:c.917C>G, XM_005252586.2:c.917C>G, XM_005252586.1:c.917C>G, NM_001007094.4:c.1187C>G, NM_001007094.3:c.1187C>G, NM_001007094.2:c.1187C>G, NM_003421.4:c.1187C>G, NM_003421.3:c.1187C>G, NM_003421.2:c.1187C>G, XM_011519658.4:c.1187C>G, XM_011519658.3:c.1187C>G, XM_011519658.2:c.1187C>G, XM_011519658.1:c.1187C>G, NM_001324259.3:c.*943C>G, NM_001324259.2:c.*943C>G, NM_001324259.1:c.*943C>G, NM_001324246.3:c.1187C>G, NM_001324246.2:c.1187C>G, NM_001324246.1:c.1187C>G, XM_011519656.3:c.1187C>G, XM_011519656.2:c.1187C>G, XM_011519656.1:c.1187C>G, NM_001324251.3:c.1187C>G, NM_001324251.2:c.1187C>G, NM_001324251.1:c.1187C>G, NM_001324250.3:c.1187C>G, NM_001324250.2:c.1187C>G, NM_001324250.1:c.1187C>G, XM_011519657.3:c.1187C>G, XM_011519657.2:c.1187C>G, XM_011519657.1:c.1187C>G, NM_001324247.3:c.1187C>G, NM_001324247.2:c.1187C>G, NM_001324247.1:c.1187C>G, NM_001324248.3:c.1187C>G, NM_001324248.2:c.1187C>G, NM_001324248.1:c.1187C>G, NM_001324249.3:c.1187C>G, NM_001324249.2:c.1187C>G, NM_001324249.1:c.1187C>G, NM_001324260.3:c.*943C>G, NM_001324260.2:c.*943C>G, NM_001324260.1:c.*943C>G, NM_001178101.3:c.1187C>G, NM_001178101.2:c.1187C>G, NM_001178101.1:c.1187C>G, NM_001324245.3:c.1187C>G, NM_001324245.2:c.1187C>G, NM_001324245.1:c.1187C>G, XM_047425722.1:c.1187C>G, XP_005252643.1:p.Ser306Ter, NP_001007095.1:p.Ser396Ter, NP_003412.1:p.Ser396Ter, XP_011517960.1:p.Ser396Ter, NP_001311175.1:p.Ser396Ter, XP_011517958.1:p.Ser396Ter, NP_001311180.1:p.Ser396Ter, NP_001311179.1:p.Ser396Ter, XP_011517959.1:p.Ser396Ter, NP_001311176.1:p.Ser396Ter, NP_001311177.1:p.Ser396Ter, NP_001311178.1:p.Ser396Ter, NP_001171572.1:p.Ser396Ter, NP_001311174.1:p.Ser396Ter, XP_047281678.1:p.Ser396Ter

                            14.

                            rs1461368084 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              10:38118347 (GRCh38)
                              10:38407275 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:38118346:T:C
                              Gene:
                              ZNF37A (Varview)
                              Functional Consequence:
                              coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,missense_variant,intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000010.11:g.38118347T>C, NC_000010.10:g.38407275T>C, XM_005252586.5:c.926T>C, XM_005252586.4:c.926T>C, XM_005252586.3:c.926T>C, XM_005252586.2:c.926T>C, XM_005252586.1:c.926T>C, NM_001007094.4:c.1196T>C, NM_001007094.3:c.1196T>C, NM_001007094.2:c.1196T>C, NM_003421.4:c.1196T>C, NM_003421.3:c.1196T>C, NM_003421.2:c.1196T>C, XM_011519658.4:c.1196T>C, XM_011519658.3:c.1196T>C, XM_011519658.2:c.1196T>C, XM_011519658.1:c.1196T>C, NM_001324259.3:c.*952T>C, NM_001324259.2:c.*952T>C, NM_001324259.1:c.*952T>C, NM_001324246.3:c.1196T>C, NM_001324246.2:c.1196T>C, NM_001324246.1:c.1196T>C, XM_011519656.3:c.1196T>C, XM_011519656.2:c.1196T>C, XM_011519656.1:c.1196T>C, NM_001324251.3:c.1196T>C, NM_001324251.2:c.1196T>C, NM_001324251.1:c.1196T>C, NM_001324250.3:c.1196T>C, NM_001324250.2:c.1196T>C, NM_001324250.1:c.1196T>C, XM_011519657.3:c.1196T>C, XM_011519657.2:c.1196T>C, XM_011519657.1:c.1196T>C, NM_001324247.3:c.1196T>C, NM_001324247.2:c.1196T>C, NM_001324247.1:c.1196T>C, NM_001324248.3:c.1196T>C, NM_001324248.2:c.1196T>C, NM_001324248.1:c.1196T>C, NM_001324249.3:c.1196T>C, NM_001324249.2:c.1196T>C, NM_001324249.1:c.1196T>C, NM_001324260.3:c.*952T>C, NM_001324260.2:c.*952T>C, NM_001324260.1:c.*952T>C, NM_001178101.3:c.1196T>C, NM_001178101.2:c.1196T>C, NM_001178101.1:c.1196T>C, NM_001324245.3:c.1196T>C, NM_001324245.2:c.1196T>C, NM_001324245.1:c.1196T>C, XM_047425722.1:c.1196T>C, XP_005252643.1:p.Ile309Thr, NP_001007095.1:p.Ile399Thr, NP_003412.1:p.Ile399Thr, XP_011517960.1:p.Ile399Thr, NP_001311175.1:p.Ile399Thr, XP_011517958.1:p.Ile399Thr, NP_001311180.1:p.Ile399Thr, NP_001311179.1:p.Ile399Thr, XP_011517959.1:p.Ile399Thr, NP_001311176.1:p.Ile399Thr, NP_001311177.1:p.Ile399Thr, NP_001311178.1:p.Ile399Thr, NP_001171572.1:p.Ile399Thr, NP_001311174.1:p.Ile399Thr, XP_047281678.1:p.Ile399Thr

                              15.

                              rs1460562528 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                10:38115277 (GRCh38)
                                10:38404205 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:38115276:C:T
                                Gene:
                                ZNF37A (Varview)
                                Functional Consequence:
                                coding_sequence_variant,synonymous_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                HGVS:
                                NC_000010.11:g.38115277C>T, NC_000010.10:g.38404205C>T, NM_001007094.4:c.225C>T, NM_001007094.3:c.225C>T, NM_001007094.2:c.225C>T, NM_003421.4:c.225C>T, NM_003421.3:c.225C>T, NM_003421.2:c.225C>T, XM_011519658.4:c.225C>T, XM_011519658.3:c.225C>T, XM_011519658.2:c.225C>T, XM_011519658.1:c.225C>T, NM_001324259.3:c.225C>T, NM_001324259.2:c.225C>T, NM_001324259.1:c.225C>T, NM_001324246.3:c.225C>T, NM_001324246.2:c.225C>T, NM_001324246.1:c.225C>T, XM_011519656.3:c.225C>T, XM_011519656.2:c.225C>T, XM_011519656.1:c.225C>T, NM_001324251.3:c.225C>T, NM_001324251.2:c.225C>T, NM_001324251.1:c.225C>T, NM_001324250.3:c.225C>T, NM_001324250.2:c.225C>T, NM_001324250.1:c.225C>T, XM_011519657.3:c.225C>T, XM_011519657.2:c.225C>T, XM_011519657.1:c.225C>T, NM_001324247.3:c.225C>T, NM_001324247.2:c.225C>T, NM_001324247.1:c.225C>T, NM_001324248.3:c.225C>T, NM_001324248.2:c.225C>T, NM_001324248.1:c.225C>T, NM_001324249.3:c.225C>T, NM_001324249.2:c.225C>T, NM_001324249.1:c.225C>T, NM_001324260.3:c.225C>T, NM_001324260.2:c.225C>T, NM_001324260.1:c.225C>T, NM_001178101.3:c.225C>T, NM_001178101.2:c.225C>T, NM_001178101.1:c.225C>T, NM_001324245.3:c.225C>T, NM_001324245.2:c.225C>T, NM_001324245.1:c.225C>T, NM_001324257.2:c.225C>T, NM_001324257.1:c.225C>T, NM_001324256.2:c.225C>T, NM_001324256.1:c.225C>T, NM_001324258.2:c.225C>T, NM_001324258.1:c.225C>T, NM_001324252.2:c.225C>T, NM_001324252.1:c.225C>T, NM_001324253.2:c.225C>T, NM_001324253.1:c.225C>T, NM_001324262.2:c.225C>T, NM_001324262.1:c.225C>T, NM_001324254.2:c.225C>T, NM_001324254.1:c.225C>T, NM_001324261.2:c.225C>T, NM_001324261.1:c.225C>T, XM_047425722.1:c.225C>T, XM_047425724.1:c.225C>T, XM_017016624.1:c.225C>T, XM_047425723.1:c.225C>T

                                16.

                                rs1457859106 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  10:38118769 (GRCh38)
                                  10:38407697 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:38118768:G:A
                                  Gene:
                                  ZNF37A (Varview)
                                  Functional Consequence:
                                  3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000010.11:g.38118769G>A, NC_000010.10:g.38407697G>A, XM_005252586.5:c.1348G>A, XM_005252586.4:c.1348G>A, XM_005252586.3:c.1348G>A, XM_005252586.2:c.1348G>A, XM_005252586.1:c.1348G>A, NM_001007094.4:c.1618G>A, NM_001007094.3:c.1618G>A, NM_001007094.2:c.1618G>A, NM_003421.4:c.1618G>A, NM_003421.3:c.1618G>A, NM_003421.2:c.1618G>A, XM_011519658.4:c.1618G>A, XM_011519658.3:c.1618G>A, XM_011519658.2:c.1618G>A, XM_011519658.1:c.1618G>A, NM_001324259.3:c.*1374G>A, NM_001324259.2:c.*1374G>A, NM_001324259.1:c.*1374G>A, NM_001324246.3:c.1618G>A, NM_001324246.2:c.1618G>A, NM_001324246.1:c.1618G>A, XM_011519656.3:c.1618G>A, XM_011519656.2:c.1618G>A, XM_011519656.1:c.1618G>A, NM_001324251.3:c.1618G>A, NM_001324251.2:c.1618G>A, NM_001324251.1:c.1618G>A, NM_001324250.3:c.1618G>A, NM_001324250.2:c.1618G>A, NM_001324250.1:c.1618G>A, XM_011519657.3:c.1618G>A, XM_011519657.2:c.1618G>A, XM_011519657.1:c.1618G>A, NM_001324247.3:c.1618G>A, NM_001324247.2:c.1618G>A, NM_001324247.1:c.1618G>A, NM_001324248.3:c.1618G>A, NM_001324248.2:c.1618G>A, NM_001324248.1:c.1618G>A, NM_001324249.3:c.1618G>A, NM_001324249.2:c.1618G>A, NM_001324249.1:c.1618G>A, NM_001324260.3:c.*1374G>A, NM_001324260.2:c.*1374G>A, NM_001324260.1:c.*1374G>A, NM_001178101.3:c.1618G>A, NM_001178101.2:c.1618G>A, NM_001178101.1:c.1618G>A, NM_001324245.3:c.1618G>A, NM_001324245.2:c.1618G>A, NM_001324245.1:c.1618G>A, XM_047425722.1:c.1618G>A, XP_005252643.1:p.Val450Ile, NP_001007095.1:p.Val540Ile, NP_003412.1:p.Val540Ile, XP_011517960.1:p.Val540Ile, NP_001311175.1:p.Val540Ile, XP_011517958.1:p.Val540Ile, NP_001311180.1:p.Val540Ile, NP_001311179.1:p.Val540Ile, XP_011517959.1:p.Val540Ile, NP_001311176.1:p.Val540Ile, NP_001311177.1:p.Val540Ile, NP_001311178.1:p.Val540Ile, NP_001171572.1:p.Val540Ile, NP_001311174.1:p.Val540Ile, XP_047281678.1:p.Val540Ile

                                  17.

                                  rs1456411568 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C,G [Show Flanks]
                                    Chromosome:
                                    10:38118693 (GRCh38)
                                    10:38407621 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:38118692:T:C,NC_000010.11:38118692:T:G
                                    Gene:
                                    ZNF37A (Varview)
                                    Functional Consequence:
                                    synonymous_variant,3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0.000071/1 (ALFA)
                                    C=0.000015/2 (GnomAD)
                                    HGVS:
                                    NC_000010.11:g.38118693T>C, NC_000010.11:g.38118693T>G, NC_000010.10:g.38407621T>C, NC_000010.10:g.38407621T>G, XM_005252586.5:c.1272T>C, XM_005252586.5:c.1272T>G, XM_005252586.4:c.1272T>C, XM_005252586.4:c.1272T>G, XM_005252586.3:c.1272T>C, XM_005252586.3:c.1272T>G, XM_005252586.2:c.1272T>C, XM_005252586.2:c.1272T>G, XM_005252586.1:c.1272T>C, XM_005252586.1:c.1272T>G, NM_001007094.4:c.1542T>C, NM_001007094.4:c.1542T>G, NM_001007094.3:c.1542T>C, NM_001007094.3:c.1542T>G, NM_001007094.2:c.1542T>C, NM_001007094.2:c.1542T>G, NM_003421.4:c.1542T>C, NM_003421.4:c.1542T>G, NM_003421.3:c.1542T>C, NM_003421.3:c.1542T>G, NM_003421.2:c.1542T>C, NM_003421.2:c.1542T>G, XM_011519658.4:c.1542T>C, XM_011519658.4:c.1542T>G, XM_011519658.3:c.1542T>C, XM_011519658.3:c.1542T>G, XM_011519658.2:c.1542T>C, XM_011519658.2:c.1542T>G, XM_011519658.1:c.1542T>C, XM_011519658.1:c.1542T>G, NM_001324259.3:c.*1298T>C, NM_001324259.3:c.*1298T>G, NM_001324259.2:c.*1298T>C, NM_001324259.2:c.*1298T>G, NM_001324259.1:c.*1298T>C, NM_001324259.1:c.*1298T>G, NM_001324246.3:c.1542T>C, NM_001324246.3:c.1542T>G, NM_001324246.2:c.1542T>C, NM_001324246.2:c.1542T>G, NM_001324246.1:c.1542T>C, NM_001324246.1:c.1542T>G, XM_011519656.3:c.1542T>C, XM_011519656.3:c.1542T>G, XM_011519656.2:c.1542T>C, XM_011519656.2:c.1542T>G, XM_011519656.1:c.1542T>C, XM_011519656.1:c.1542T>G, NM_001324251.3:c.1542T>C, NM_001324251.3:c.1542T>G, NM_001324251.2:c.1542T>C, NM_001324251.2:c.1542T>G, NM_001324251.1:c.1542T>C, NM_001324251.1:c.1542T>G, NM_001324250.3:c.1542T>C, NM_001324250.3:c.1542T>G, NM_001324250.2:c.1542T>C, NM_001324250.2:c.1542T>G, NM_001324250.1:c.1542T>C, NM_001324250.1:c.1542T>G, XM_011519657.3:c.1542T>C, XM_011519657.3:c.1542T>G, XM_011519657.2:c.1542T>C, XM_011519657.2:c.1542T>G, XM_011519657.1:c.1542T>C, XM_011519657.1:c.1542T>G, NM_001324247.3:c.1542T>C, NM_001324247.3:c.1542T>G, NM_001324247.2:c.1542T>C, NM_001324247.2:c.1542T>G, NM_001324247.1:c.1542T>C, NM_001324247.1:c.1542T>G, NM_001324248.3:c.1542T>C, NM_001324248.3:c.1542T>G, NM_001324248.2:c.1542T>C, NM_001324248.2:c.1542T>G, NM_001324248.1:c.1542T>C, NM_001324248.1:c.1542T>G, NM_001324249.3:c.1542T>C, NM_001324249.3:c.1542T>G, NM_001324249.2:c.1542T>C, NM_001324249.2:c.1542T>G, NM_001324249.1:c.1542T>C, NM_001324249.1:c.1542T>G, NM_001324260.3:c.*1298T>C, NM_001324260.3:c.*1298T>G, NM_001324260.2:c.*1298T>C, NM_001324260.2:c.*1298T>G, NM_001324260.1:c.*1298T>C, NM_001324260.1:c.*1298T>G, NM_001178101.3:c.1542T>C, NM_001178101.3:c.1542T>G, NM_001178101.2:c.1542T>C, NM_001178101.2:c.1542T>G, NM_001178101.1:c.1542T>C, NM_001178101.1:c.1542T>G, NM_001324245.3:c.1542T>C, NM_001324245.3:c.1542T>G, NM_001324245.2:c.1542T>C, NM_001324245.2:c.1542T>G, NM_001324245.1:c.1542T>C, NM_001324245.1:c.1542T>G, XM_047425722.1:c.1542T>C, XM_047425722.1:c.1542T>G, XP_005252643.1:p.His424Gln, NP_001007095.1:p.His514Gln, NP_003412.1:p.His514Gln, XP_011517960.1:p.His514Gln, NP_001311175.1:p.His514Gln, XP_011517958.1:p.His514Gln, NP_001311180.1:p.His514Gln, NP_001311179.1:p.His514Gln, XP_011517959.1:p.His514Gln, NP_001311176.1:p.His514Gln, NP_001311177.1:p.His514Gln, NP_001311178.1:p.His514Gln, NP_001171572.1:p.His514Gln, NP_001311174.1:p.His514Gln, XP_047281678.1:p.His514Gln

                                    18.

                                    rs1455644945 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>C [Show Flanks]
                                      Chromosome:
                                      10:38118418 (GRCh38)
                                      10:38407346 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:38118417:A:C
                                      Gene:
                                      ZNF37A (Varview)
                                      Functional Consequence:
                                      3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000004/1 (TOPMED)
                                      HGVS:
                                      NC_000010.11:g.38118418A>C, NC_000010.10:g.38407346A>C, XM_005252586.5:c.997A>C, XM_005252586.4:c.997A>C, XM_005252586.3:c.997A>C, XM_005252586.2:c.997A>C, XM_005252586.1:c.997A>C, NM_001007094.4:c.1267A>C, NM_001007094.3:c.1267A>C, NM_001007094.2:c.1267A>C, NM_003421.4:c.1267A>C, NM_003421.3:c.1267A>C, NM_003421.2:c.1267A>C, XM_011519658.4:c.1267A>C, XM_011519658.3:c.1267A>C, XM_011519658.2:c.1267A>C, XM_011519658.1:c.1267A>C, NM_001324259.3:c.*1023A>C, NM_001324259.2:c.*1023A>C, NM_001324259.1:c.*1023A>C, NM_001324246.3:c.1267A>C, NM_001324246.2:c.1267A>C, NM_001324246.1:c.1267A>C, XM_011519656.3:c.1267A>C, XM_011519656.2:c.1267A>C, XM_011519656.1:c.1267A>C, NM_001324251.3:c.1267A>C, NM_001324251.2:c.1267A>C, NM_001324251.1:c.1267A>C, NM_001324250.3:c.1267A>C, NM_001324250.2:c.1267A>C, NM_001324250.1:c.1267A>C, XM_011519657.3:c.1267A>C, XM_011519657.2:c.1267A>C, XM_011519657.1:c.1267A>C, NM_001324247.3:c.1267A>C, NM_001324247.2:c.1267A>C, NM_001324247.1:c.1267A>C, NM_001324248.3:c.1267A>C, NM_001324248.2:c.1267A>C, NM_001324248.1:c.1267A>C, NM_001324249.3:c.1267A>C, NM_001324249.2:c.1267A>C, NM_001324249.1:c.1267A>C, NM_001324260.3:c.*1023A>C, NM_001324260.2:c.*1023A>C, NM_001324260.1:c.*1023A>C, NM_001178101.3:c.1267A>C, NM_001178101.2:c.1267A>C, NM_001178101.1:c.1267A>C, NM_001324245.3:c.1267A>C, NM_001324245.2:c.1267A>C, NM_001324245.1:c.1267A>C, XM_047425722.1:c.1267A>C, XP_005252643.1:p.Lys333Gln, NP_001007095.1:p.Lys423Gln, NP_003412.1:p.Lys423Gln, XP_011517960.1:p.Lys423Gln, NP_001311175.1:p.Lys423Gln, XP_011517958.1:p.Lys423Gln, NP_001311180.1:p.Lys423Gln, NP_001311179.1:p.Lys423Gln, XP_011517959.1:p.Lys423Gln, NP_001311176.1:p.Lys423Gln, NP_001311177.1:p.Lys423Gln, NP_001311178.1:p.Lys423Gln, NP_001171572.1:p.Lys423Gln, NP_001311174.1:p.Lys423Gln, XP_047281678.1:p.Lys423Gln

                                      19.

                                      rs1450358422 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        AA>- [Show Flanks]
                                        Chromosome:
                                        10:38118377 (GRCh38)
                                        10:38407305 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:38118373:AAAAA:AAA
                                        Gene:
                                        ZNF37A (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant,frameshift_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        AAA=0./0 (ALFA)
                                        -=0.000004/1 (GnomAD_exomes)
                                        -=0.000004/1 (TOPMED)
                                        -=0.000007/1 (GnomAD)
                                        HGVS:
                                        NC_000010.11:g.38118377_38118378del, NC_000010.10:g.38407305_38407306del, XM_005252586.5:c.956_957del, XM_005252586.4:c.956_957del, XM_005252586.3:c.956_957del, XM_005252586.2:c.956_957del, XM_005252586.1:c.956_957del, NM_001007094.4:c.1226_1227del, NM_001007094.3:c.1226_1227del, NM_001007094.2:c.1226_1227del, NM_003421.4:c.1226_1227del, NM_003421.3:c.1226_1227del, NM_003421.2:c.1226_1227del, XM_011519658.4:c.1226_1227del, XM_011519658.3:c.1226_1227del, XM_011519658.2:c.1226_1227del, XM_011519658.1:c.1226_1227del, NM_001324259.3:c.*982_*983del, NM_001324259.2:c.*982_*983del, NM_001324259.1:c.*982_*983del, NM_001324246.3:c.1226_1227del, NM_001324246.2:c.1226_1227del, NM_001324246.1:c.1226_1227del, XM_011519656.3:c.1226_1227del, XM_011519656.2:c.1226_1227del, XM_011519656.1:c.1226_1227del, NM_001324251.3:c.1226_1227del, NM_001324251.2:c.1226_1227del, NM_001324251.1:c.1226_1227del, NM_001324250.3:c.1226_1227del, NM_001324250.2:c.1226_1227del, NM_001324250.1:c.1226_1227del, XM_011519657.3:c.1226_1227del, XM_011519657.2:c.1226_1227del, XM_011519657.1:c.1226_1227del, NM_001324247.3:c.1226_1227del, NM_001324247.2:c.1226_1227del, NM_001324247.1:c.1226_1227del, NM_001324248.3:c.1226_1227del, NM_001324248.2:c.1226_1227del, NM_001324248.1:c.1226_1227del, NM_001324249.3:c.1226_1227del, NM_001324249.2:c.1226_1227del, NM_001324249.1:c.1226_1227del, NM_001324260.3:c.*982_*983del, NM_001324260.2:c.*982_*983del, NM_001324260.1:c.*982_*983del, NM_001178101.3:c.1226_1227del, NM_001178101.2:c.1226_1227del, NM_001178101.1:c.1226_1227del, NM_001324245.3:c.1226_1227del, NM_001324245.2:c.1226_1227del, NM_001324245.1:c.1226_1227del, XM_047425722.1:c.1226_1227del, XP_005252643.1:p.Lys319fs, NP_001007095.1:p.Lys409fs, NP_003412.1:p.Lys409fs, XP_011517960.1:p.Lys409fs, NP_001311175.1:p.Lys409fs, XP_011517958.1:p.Lys409fs, NP_001311180.1:p.Lys409fs, NP_001311179.1:p.Lys409fs, XP_011517959.1:p.Lys409fs, NP_001311176.1:p.Lys409fs, NP_001311177.1:p.Lys409fs, NP_001311178.1:p.Lys409fs, NP_001171572.1:p.Lys409fs, NP_001311174.1:p.Lys409fs, XP_047281678.1:p.Lys409fs

                                        20.

                                        rs1448927248 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>T [Show Flanks]
                                          Chromosome:
                                          10:38117857 (GRCh38)
                                          10:38406785 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:38117856:A:T
                                          Gene:
                                          ZNF37A (Varview)
                                          Functional Consequence:
                                          3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0.000004/1 (GnomAD_exomes)
                                          T=0.000004/1 (TOPMED)
                                          T=0.000007/1 (GnomAD)
                                          HGVS:
                                          NC_000010.11:g.38117857A>T, NC_000010.10:g.38406785A>T, XM_005252586.5:c.436A>T, XM_005252586.4:c.436A>T, XM_005252586.3:c.436A>T, XM_005252586.2:c.436A>T, XM_005252586.1:c.436A>T, NM_001007094.4:c.706A>T, NM_001007094.3:c.706A>T, NM_001007094.2:c.706A>T, NM_003421.4:c.706A>T, NM_003421.3:c.706A>T, NM_003421.2:c.706A>T, XM_011519658.4:c.706A>T, XM_011519658.3:c.706A>T, XM_011519658.2:c.706A>T, XM_011519658.1:c.706A>T, NM_001324259.3:c.*462A>T, NM_001324259.2:c.*462A>T, NM_001324259.1:c.*462A>T, NM_001324246.3:c.706A>T, NM_001324246.2:c.706A>T, NM_001324246.1:c.706A>T, XM_011519656.3:c.706A>T, XM_011519656.2:c.706A>T, XM_011519656.1:c.706A>T, NM_001324251.3:c.706A>T, NM_001324251.2:c.706A>T, NM_001324251.1:c.706A>T, NM_001324250.3:c.706A>T, NM_001324250.2:c.706A>T, NM_001324250.1:c.706A>T, XM_011519657.3:c.706A>T, XM_011519657.2:c.706A>T, XM_011519657.1:c.706A>T, NM_001324247.3:c.706A>T, NM_001324247.2:c.706A>T, NM_001324247.1:c.706A>T, NM_001324248.3:c.706A>T, NM_001324248.2:c.706A>T, NM_001324248.1:c.706A>T, NM_001324249.3:c.706A>T, NM_001324249.2:c.706A>T, NM_001324249.1:c.706A>T, NM_001324260.3:c.*462A>T, NM_001324260.2:c.*462A>T, NM_001324260.1:c.*462A>T, NM_001178101.3:c.706A>T, NM_001178101.2:c.706A>T, NM_001178101.1:c.706A>T, NM_001324245.3:c.706A>T, NM_001324245.2:c.706A>T, NM_001324245.1:c.706A>T, XM_047425722.1:c.706A>T, XP_005252643.1:p.Thr146Ser, NP_001007095.1:p.Thr236Ser, NP_003412.1:p.Thr236Ser, XP_011517960.1:p.Thr236Ser, NP_001311175.1:p.Thr236Ser, XP_011517958.1:p.Thr236Ser, NP_001311180.1:p.Thr236Ser, NP_001311179.1:p.Thr236Ser, XP_011517959.1:p.Thr236Ser, NP_001311176.1:p.Thr236Ser, NP_001311177.1:p.Thr236Ser, NP_001311178.1:p.Thr236Ser, NP_001171572.1:p.Thr236Ser, NP_001311174.1:p.Thr236Ser, XP_047281678.1:p.Thr236Ser

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