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Items: 1 to 20 of 932

1.

rs1490244440 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    19:1625664 (GRCh38)
    19:1625663 (GRCh37)
    Canonical SPDI:
    NC_000019.10:1625663:G:A
    Gene:
    TCF3 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0.000004/1 (TOPMED)
    A=0.000007/1 (GnomAD)
    HGVS:
    NC_000019.10:g.1625664G>A, NC_000019.9:g.1625663G>A, NG_029953.2:g.31883C>T, NM_003200.5:c.411C>T, NM_003200.4:c.411C>T, NM_003200.3:c.411C>T, NM_001136139.4:c.411C>T, NM_001136139.3:c.411C>T, NM_001136139.2:c.411C>T, NM_001351779.2:c.411C>T, NM_001351779.1:c.411C>T, NM_001351778.2:c.411C>T, NM_001351778.1:c.411C>T, XM_006722855.5:c.498C>T, XM_006722855.4:c.498C>T, XM_006722855.3:c.498C>T, XM_006722855.2:c.498C>T, XM_006722855.1:c.498C>T, XM_011528226.3:c.411C>T, XM_011528226.2:c.411C>T, XM_011528226.1:c.411C>T, XM_011528225.3:c.411C>T, XM_011528225.2:c.411C>T, XM_011528225.1:c.411C>T, XM_017027181.2:c.411C>T, XM_017027181.1:c.411C>T, XM_017027178.2:c.498C>T, XM_017027178.1:c.498C>T, XM_047439270.1:c.411C>T, XM_047439275.1:c.411C>T, XM_047439263.1:c.411C>T, XM_047439266.1:c.411C>T, XM_047439272.1:c.411C>T, XM_047439271.1:c.411C>T, XM_047439292.1:c.258C>T, XM_047439264.1:c.411C>T, XM_047439267.1:c.411C>T, XM_047439268.1:c.411C>T, XM_047439273.1:c.411C>T, XM_047439293.1:c.258C>T, XM_047439276.1:c.411C>T, XM_047439281.1:c.411C>T, XM_047439258.1:c.498C>T, XM_047439261.1:c.498C>T, XM_047439279.1:c.411C>T, XM_047439282.1:c.411C>T, XM_047439291.1:c.411C>T, XM_047439286.1:c.411C>T, XM_047439285.1:c.411C>T, XM_047439290.1:c.411C>T, XM_047439295.1:c.258C>T, XM_047439294.1:c.258C>T, XM_047439297.1:c.258C>T, XM_047439298.1:c.258C>T, XM_047439265.1:c.411C>T, XM_047439269.1:c.411C>T, XM_047439288.1:c.411C>T, XM_047439274.1:c.411C>T, XM_047439260.1:c.498C>T, XM_047439262.1:c.498C>T, XM_047439280.1:c.411C>T, XM_047439277.1:c.411C>T, XM_047439287.1:c.411C>T, XM_047439283.1:c.411C>T, XM_047439296.1:c.258C>T, XM_047439259.1:c.498C>T, XM_047439278.1:c.411C>T, XM_047439289.1:c.411C>T, XM_047439284.1:c.411C>T

    2.

    rs1489122279 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      19:1611764 (GRCh38)
      19:1611763 (GRCh37)
      Canonical SPDI:
      NC_000019.10:1611763:C:T
      Gene:
      TCF3 (Varview)
      Functional Consequence:
      synonymous_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0./0 (ALFA)
      T=0.000007/1 (GnomAD)
      HGVS:
      NC_000019.10:g.1611764C>T, NC_000019.9:g.1611763C>T, NG_029953.2:g.45783G>A, NM_003200.5:c.1908G>A, NM_003200.4:c.1908G>A, NM_003200.3:c.1908G>A, NM_001136139.4:c.1899G>A, NM_001136139.3:c.1899G>A, NM_001136139.2:c.1899G>A, NM_001351779.2:c.1899G>A, NM_001351779.1:c.1899G>A, NM_001351778.2:c.1905G>A, NM_001351778.1:c.1905G>A, XM_006722855.5:c.1986G>A, XM_006722855.4:c.1986G>A, XM_006722855.3:c.1986G>A, XM_006722855.2:c.1986G>A, XM_006722855.1:c.1986G>A, XM_011528226.3:c.1896G>A, XM_011528226.2:c.1896G>A, XM_011528226.1:c.1896G>A, XM_011528225.3:c.1896G>A, XM_011528225.2:c.1896G>A, XM_011528225.1:c.1896G>A, XM_017027181.2:c.1908G>A, XM_017027181.1:c.1908G>A, XM_017027178.2:c.1986G>A, XM_017027178.1:c.1986G>A, XM_047439270.1:c.1896G>A, XM_047439275.1:c.1893G>A, XM_047439263.1:c.1908G>A, XM_047439266.1:c.1905G>A, XM_047439272.1:c.1896G>A, XM_047439271.1:c.1896G>A, XM_047439292.1:c.1746G>A, XM_047439264.1:c.1908G>A, XM_047439267.1:c.1905G>A, XM_047439268.1:c.1899G>A, XM_047439273.1:c.1896G>A, XM_047439293.1:c.1746G>A, XM_047439276.1:c.1908G>A, XM_047439281.1:c.1899G>A, XM_047439258.1:c.1995G>A, XM_047439261.1:c.1992G>A, XM_047439279.1:c.1905G>A, XM_047439282.1:c.1899G>A, XM_047439291.1:c.1893G>A, XM_047439286.1:c.1896G>A, XM_047439285.1:c.1896G>A, XM_047439290.1:c.1893G>A, XM_047439295.1:c.1755G>A, XM_047439294.1:c.1755G>A, XM_047439297.1:c.1746G>A, XM_047439298.1:c.1743G>A, XM_047439265.1:c.1908G>A, XM_047439269.1:c.1899G>A, XM_047439288.1:c.1896G>A, XM_047439274.1:c.1896G>A, XM_047439260.1:c.1995G>A, XM_047439262.1:c.1986G>A, XM_047439280.1:c.1905G>A, XM_047439277.1:c.1908G>A, XM_047439287.1:c.1896G>A, XM_047439283.1:c.1899G>A, XM_047439296.1:c.1755G>A, XM_047439259.1:c.1995G>A, XM_047439278.1:c.1908G>A, XM_047439289.1:c.1896G>A, XM_047439284.1:c.1899G>A

      3.

      rs1488005407 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C [Show Flanks]
        Chromosome:
        19:1612368 (GRCh38)
        19:1612367 (GRCh37)
        Canonical SPDI:
        NC_000019.10:1612367:T:C
        Gene:
        TCF3 (Varview)
        Functional Consequence:
        missense_variant,intron_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0./0 (ALFA)
        C=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000019.10:g.1612368T>C, NC_000019.9:g.1612367T>C, NG_029953.2:g.45179A>G, NM_001136139.4:c.1652A>G, NM_001136139.3:c.1652A>G, NM_001136139.2:c.1652A>G, NM_001351779.2:c.1652A>G, NM_001351779.1:c.1652A>G, XM_006722855.5:c.1739A>G, XM_006722855.4:c.1739A>G, XM_006722855.3:c.1739A>G, XM_006722855.2:c.1739A>G, XM_006722855.1:c.1739A>G, XM_011528226.3:c.1649A>G, XM_011528226.2:c.1649A>G, XM_011528226.1:c.1649A>G, XM_011528225.3:c.1649A>G, XM_011528225.2:c.1649A>G, XM_011528225.1:c.1649A>G, XM_017027178.2:c.1739A>G, XM_017027178.1:c.1739A>G, XM_047439270.1:c.1649A>G, XM_047439275.1:c.1646A>G, XM_047439272.1:c.1649A>G, XM_047439271.1:c.1649A>G, XM_047439292.1:c.1499A>G, XM_047439268.1:c.1652A>G, XM_047439273.1:c.1649A>G, XM_047439293.1:c.1499A>G, XM_047439281.1:c.1652A>G, XM_047439282.1:c.1652A>G, XM_047439291.1:c.1646A>G, XM_047439286.1:c.1649A>G, XM_047439285.1:c.1649A>G, XM_047439290.1:c.1646A>G, XM_047439297.1:c.1499A>G, XM_047439298.1:c.1496A>G, XM_047439269.1:c.1652A>G, XM_047439288.1:c.1649A>G, XM_047439274.1:c.1649A>G, XM_047439262.1:c.1739A>G, XM_047439287.1:c.1649A>G, XM_047439283.1:c.1652A>G, XM_047439289.1:c.1649A>G, XM_047439284.1:c.1652A>G, NP_001129611.1:p.Asn551Ser, NP_001338708.1:p.Asn551Ser, XP_006722918.1:p.Asn580Ser, XP_011526528.1:p.Asn550Ser, XP_011526527.1:p.Asn550Ser, XP_016882667.1:p.Asn580Ser, XP_047295226.1:p.Asn550Ser, XP_047295231.1:p.Asn549Ser, XP_047295228.1:p.Asn550Ser, XP_047295227.1:p.Asn550Ser, XP_047295248.1:p.Asn500Ser, XP_047295224.1:p.Asn551Ser, XP_047295229.1:p.Asn550Ser, XP_047295249.1:p.Asn500Ser, XP_047295237.1:p.Asn551Ser, XP_047295238.1:p.Asn551Ser, XP_047295247.1:p.Asn549Ser, XP_047295242.1:p.Asn550Ser, XP_047295241.1:p.Asn550Ser, XP_047295246.1:p.Asn549Ser, XP_047295253.1:p.Asn500Ser, XP_047295254.1:p.Asn499Ser, XP_047295225.1:p.Asn551Ser, XP_047295244.1:p.Asn550Ser, XP_047295230.1:p.Asn550Ser, XP_047295218.1:p.Asn580Ser, XP_047295243.1:p.Asn550Ser, XP_047295239.1:p.Asn551Ser, XP_047295245.1:p.Asn550Ser, XP_047295240.1:p.Asn551Ser

        4.

        rs1487181959 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>C [Show Flanks]
          Chromosome:
          19:1632351 (GRCh38)
          19:1632350 (GRCh37)
          Canonical SPDI:
          NC_000019.10:1632350:G:C
          Gene:
          TCF3 (Varview)
          Functional Consequence:
          missense_variant,intron_variant,coding_sequence_variant
          Validated:
          by frequency
          MAF:
          C=0.00001/2 (GnomAD_exomes)
          HGVS:
          NC_000019.10:g.1632351G>C, NC_000019.9:g.1632350G>C, NG_029953.2:g.25196C>G, NM_003200.5:c.200C>G, NM_003200.4:c.200C>G, NM_003200.3:c.200C>G, NM_001136139.4:c.200C>G, NM_001136139.3:c.200C>G, NM_001136139.2:c.200C>G, NM_001351779.2:c.200C>G, NM_001351779.1:c.200C>G, NM_001351778.2:c.200C>G, NM_001351778.1:c.200C>G, XM_006722855.5:c.200C>G, XM_006722855.4:c.200C>G, XM_006722855.3:c.200C>G, XM_006722855.2:c.200C>G, XM_006722855.1:c.200C>G, XM_011528226.3:c.200C>G, XM_011528226.2:c.200C>G, XM_011528226.1:c.200C>G, XM_011528225.3:c.200C>G, XM_011528225.2:c.200C>G, XM_011528225.1:c.200C>G, XM_017027181.2:c.200C>G, XM_017027181.1:c.200C>G, XM_017027178.2:c.200C>G, XM_017027178.1:c.200C>G, XM_047439270.1:c.200C>G, XM_047439275.1:c.200C>G, XM_047439263.1:c.200C>G, XM_047439266.1:c.200C>G, XM_047439272.1:c.200C>G, XM_047439271.1:c.200C>G, XM_047439264.1:c.200C>G, XM_047439267.1:c.200C>G, XM_047439268.1:c.200C>G, XM_047439273.1:c.200C>G, XM_047439276.1:c.200C>G, XM_047439281.1:c.200C>G, XM_047439258.1:c.200C>G, XM_047439261.1:c.200C>G, XM_047439279.1:c.200C>G, XM_047439282.1:c.200C>G, XM_047439291.1:c.200C>G, XM_047439286.1:c.200C>G, XM_047439285.1:c.200C>G, XM_047439290.1:c.200C>G, XM_047439265.1:c.200C>G, XM_047439269.1:c.200C>G, XM_047439288.1:c.200C>G, XM_047439274.1:c.200C>G, XM_047439260.1:c.200C>G, XM_047439262.1:c.200C>G, XM_047439280.1:c.200C>G, XM_047439277.1:c.200C>G, XM_047439287.1:c.200C>G, XM_047439283.1:c.200C>G, XM_047439259.1:c.200C>G, XM_047439278.1:c.200C>G, XM_047439289.1:c.200C>G, XM_047439284.1:c.200C>G, NP_003191.1:p.Ser67Cys, NP_001129611.1:p.Ser67Cys, NP_001338708.1:p.Ser67Cys, NP_001338707.1:p.Ser67Cys, XP_006722918.1:p.Ser67Cys, XP_011526528.1:p.Ser67Cys, XP_011526527.1:p.Ser67Cys, XP_016882670.1:p.Ser67Cys, XP_016882667.1:p.Ser67Cys, XP_047295226.1:p.Ser67Cys, XP_047295231.1:p.Ser67Cys, XP_047295219.1:p.Ser67Cys, XP_047295222.1:p.Ser67Cys, XP_047295228.1:p.Ser67Cys, XP_047295227.1:p.Ser67Cys, XP_047295220.1:p.Ser67Cys, XP_047295223.1:p.Ser67Cys, XP_047295224.1:p.Ser67Cys, XP_047295229.1:p.Ser67Cys, XP_047295232.1:p.Ser67Cys, XP_047295237.1:p.Ser67Cys, XP_047295214.1:p.Ser67Cys, XP_047295217.1:p.Ser67Cys, XP_047295235.1:p.Ser67Cys, XP_047295238.1:p.Ser67Cys, XP_047295247.1:p.Ser67Cys, XP_047295242.1:p.Ser67Cys, XP_047295241.1:p.Ser67Cys, XP_047295246.1:p.Ser67Cys, XP_047295221.1:p.Ser67Cys, XP_047295225.1:p.Ser67Cys, XP_047295244.1:p.Ser67Cys, XP_047295230.1:p.Ser67Cys, XP_047295216.1:p.Ser67Cys, XP_047295218.1:p.Ser67Cys, XP_047295236.1:p.Ser67Cys, XP_047295233.1:p.Ser67Cys, XP_047295243.1:p.Ser67Cys, XP_047295239.1:p.Ser67Cys, XP_047295215.1:p.Ser67Cys, XP_047295234.1:p.Ser67Cys, XP_047295245.1:p.Ser67Cys, XP_047295240.1:p.Ser67Cys

          5.

          rs1485706155 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            GGA>- [Show Flanks]
            Chromosome:
            19:1622187 (GRCh38)
            19:1622186 (GRCh37)
            Canonical SPDI:
            NC_000019.10:1622186:GGA:
            Gene:
            TCF3 (Varview)
            Functional Consequence:
            inframe_deletion,coding_sequence_variant
            Validated:
            by frequency,by cluster
            MAF:
            -=0.000007/1 (GnomAD)
            HGVS:
            NC_000019.10:g.1622187_1622189del, NC_000019.9:g.1622186_1622188del, NG_029953.2:g.35358_35360del, NM_003200.5:c.687_689del, NM_003200.4:c.687_689del, NM_003200.3:c.687_689del, NM_001136139.4:c.687_689del, NM_001136139.3:c.687_689del, NM_001136139.2:c.687_689del, NM_001351779.2:c.687_689del, NM_001351779.1:c.687_689del, NM_001351778.2:c.687_689del, NM_001351778.1:c.687_689del, XM_006722855.5:c.774_776del, XM_006722855.4:c.774_776del, XM_006722855.3:c.774_776del, XM_006722855.2:c.774_776del, XM_006722855.1:c.774_776del, XM_011528226.3:c.687_689del, XM_011528226.2:c.687_689del, XM_011528226.1:c.687_689del, XM_011528225.3:c.687_689del, XM_011528225.2:c.687_689del, XM_011528225.1:c.687_689del, XM_017027181.2:c.687_689del, XM_017027181.1:c.687_689del, XM_017027178.2:c.774_776del, XM_017027178.1:c.774_776del, XM_047439270.1:c.687_689del, XM_047439275.1:c.687_689del, XM_047439263.1:c.687_689del, XM_047439266.1:c.687_689del, XM_047439272.1:c.687_689del, XM_047439271.1:c.687_689del, XM_047439292.1:c.534_536del, XM_047439264.1:c.687_689del, XM_047439267.1:c.687_689del, XM_047439268.1:c.687_689del, XM_047439273.1:c.687_689del, XM_047439293.1:c.534_536del, XM_047439276.1:c.687_689del, XM_047439281.1:c.687_689del, XM_047439258.1:c.774_776del, XM_047439261.1:c.774_776del, XM_047439279.1:c.687_689del, XM_047439282.1:c.687_689del, XM_047439291.1:c.687_689del, XM_047439286.1:c.687_689del, XM_047439285.1:c.687_689del, XM_047439290.1:c.687_689del, XM_047439295.1:c.534_536del, XM_047439294.1:c.534_536del, XM_047439297.1:c.534_536del, XM_047439298.1:c.534_536del, XM_047439265.1:c.687_689del, XM_047439269.1:c.687_689del, XM_047439288.1:c.687_689del, XM_047439274.1:c.687_689del, XM_047439260.1:c.774_776del, XM_047439262.1:c.774_776del, XM_047439280.1:c.687_689del, XM_047439277.1:c.687_689del, XM_047439287.1:c.687_689del, XM_047439283.1:c.687_689del, XM_047439296.1:c.534_536del, XM_047439259.1:c.774_776del, XM_047439278.1:c.687_689del, XM_047439289.1:c.687_689del, XM_047439284.1:c.687_689del, NP_003191.1:p.Pro231del, NP_001129611.1:p.Pro231del, NP_001338708.1:p.Pro231del, NP_001338707.1:p.Pro231del, XP_006722918.1:p.Pro260del, XP_011526528.1:p.Pro231del, XP_011526527.1:p.Pro231del, XP_016882670.1:p.Pro231del, XP_016882667.1:p.Pro260del, XP_047295226.1:p.Pro231del, XP_047295231.1:p.Pro231del, XP_047295219.1:p.Pro231del, XP_047295222.1:p.Pro231del, XP_047295228.1:p.Pro231del, XP_047295227.1:p.Pro231del, XP_047295248.1:p.Pro180del, XP_047295220.1:p.Pro231del, XP_047295223.1:p.Pro231del, XP_047295224.1:p.Pro231del, XP_047295229.1:p.Pro231del, XP_047295249.1:p.Pro180del, XP_047295232.1:p.Pro231del, XP_047295237.1:p.Pro231del, XP_047295214.1:p.Pro260del, XP_047295217.1:p.Pro260del, XP_047295235.1:p.Pro231del, XP_047295238.1:p.Pro231del, XP_047295247.1:p.Pro231del, XP_047295242.1:p.Pro231del, XP_047295241.1:p.Pro231del, XP_047295246.1:p.Pro231del, XP_047295251.1:p.Pro180del, XP_047295250.1:p.Pro180del, XP_047295253.1:p.Pro180del, XP_047295254.1:p.Pro180del, XP_047295221.1:p.Pro231del, XP_047295225.1:p.Pro231del, XP_047295244.1:p.Pro231del, XP_047295230.1:p.Pro231del, XP_047295216.1:p.Pro260del, XP_047295218.1:p.Pro260del, XP_047295236.1:p.Pro231del, XP_047295233.1:p.Pro231del, XP_047295243.1:p.Pro231del, XP_047295239.1:p.Pro231del, XP_047295252.1:p.Pro180del, XP_047295215.1:p.Pro260del, XP_047295234.1:p.Pro231del, XP_047295245.1:p.Pro231del, XP_047295240.1:p.Pro231del

            6.

            rs1484552955 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              19:1621923 (GRCh38)
              19:1621922 (GRCh37)
              Canonical SPDI:
              NC_000019.10:1621922:T:C
              Gene:
              TCF3 (Varview)
              Functional Consequence:
              synonymous_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              C=0.000004/1 (GnomAD_exomes)
              C=0.000019/5 (TOPMED)
              C=0.000021/3 (GnomAD)
              HGVS:
              NC_000019.10:g.1621923T>C, NC_000019.9:g.1621922T>C, NG_029953.2:g.35624A>G, NM_003200.5:c.870A>G, NM_003200.4:c.870A>G, NM_003200.3:c.870A>G, NM_001136139.4:c.870A>G, NM_001136139.3:c.870A>G, NM_001136139.2:c.870A>G, NM_001351779.2:c.870A>G, NM_001351779.1:c.870A>G, NM_001351778.2:c.870A>G, NM_001351778.1:c.870A>G, XM_006722855.5:c.957A>G, XM_006722855.4:c.957A>G, XM_006722855.3:c.957A>G, XM_006722855.2:c.957A>G, XM_006722855.1:c.957A>G, XM_011528226.3:c.870A>G, XM_011528226.2:c.870A>G, XM_011528226.1:c.870A>G, XM_011528225.3:c.870A>G, XM_011528225.2:c.870A>G, XM_011528225.1:c.870A>G, XM_017027181.2:c.870A>G, XM_017027181.1:c.870A>G, XM_017027178.2:c.957A>G, XM_017027178.1:c.957A>G, XM_047439270.1:c.870A>G, XM_047439275.1:c.870A>G, XM_047439263.1:c.870A>G, XM_047439266.1:c.870A>G, XM_047439272.1:c.870A>G, XM_047439271.1:c.870A>G, XM_047439292.1:c.717A>G, XM_047439264.1:c.870A>G, XM_047439267.1:c.870A>G, XM_047439268.1:c.870A>G, XM_047439273.1:c.870A>G, XM_047439293.1:c.717A>G, XM_047439276.1:c.870A>G, XM_047439281.1:c.870A>G, XM_047439258.1:c.957A>G, XM_047439261.1:c.957A>G, XM_047439279.1:c.870A>G, XM_047439282.1:c.870A>G, XM_047439291.1:c.870A>G, XM_047439286.1:c.870A>G, XM_047439285.1:c.870A>G, XM_047439290.1:c.870A>G, XM_047439295.1:c.717A>G, XM_047439294.1:c.717A>G, XM_047439297.1:c.717A>G, XM_047439298.1:c.717A>G, XM_047439265.1:c.870A>G, XM_047439269.1:c.870A>G, XM_047439288.1:c.870A>G, XM_047439274.1:c.870A>G, XM_047439260.1:c.957A>G, XM_047439262.1:c.957A>G, XM_047439280.1:c.870A>G, XM_047439277.1:c.870A>G, XM_047439287.1:c.870A>G, XM_047439283.1:c.870A>G, XM_047439296.1:c.717A>G, XM_047439259.1:c.957A>G, XM_047439278.1:c.870A>G, XM_047439289.1:c.870A>G, XM_047439284.1:c.870A>G

              7.

              rs1482835647 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                19:1632397 (GRCh38)
                19:1632396 (GRCh37)
                Canonical SPDI:
                NC_000019.10:1632396:C:T
                Gene:
                TCF3 (Varview)
                Functional Consequence:
                missense_variant,intron_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                T=0.000004/1 (TOPMED)
                HGVS:
                NC_000019.10:g.1632397C>T, NC_000019.9:g.1632396C>T, NG_029953.2:g.25150G>A, NM_003200.5:c.154G>A, NM_003200.4:c.154G>A, NM_003200.3:c.154G>A, NM_001136139.4:c.154G>A, NM_001136139.3:c.154G>A, NM_001136139.2:c.154G>A, NM_001351779.2:c.154G>A, NM_001351779.1:c.154G>A, NM_001351778.2:c.154G>A, NM_001351778.1:c.154G>A, XM_006722855.5:c.154G>A, XM_006722855.4:c.154G>A, XM_006722855.3:c.154G>A, XM_006722855.2:c.154G>A, XM_006722855.1:c.154G>A, XM_011528226.3:c.154G>A, XM_011528226.2:c.154G>A, XM_011528226.1:c.154G>A, XM_011528225.3:c.154G>A, XM_011528225.2:c.154G>A, XM_011528225.1:c.154G>A, XM_017027181.2:c.154G>A, XM_017027181.1:c.154G>A, XM_017027178.2:c.154G>A, XM_017027178.1:c.154G>A, XM_047439270.1:c.154G>A, XM_047439275.1:c.154G>A, XM_047439263.1:c.154G>A, XM_047439266.1:c.154G>A, XM_047439272.1:c.154G>A, XM_047439271.1:c.154G>A, XM_047439264.1:c.154G>A, XM_047439267.1:c.154G>A, XM_047439268.1:c.154G>A, XM_047439273.1:c.154G>A, XM_047439276.1:c.154G>A, XM_047439281.1:c.154G>A, XM_047439258.1:c.154G>A, XM_047439261.1:c.154G>A, XM_047439279.1:c.154G>A, XM_047439282.1:c.154G>A, XM_047439291.1:c.154G>A, XM_047439286.1:c.154G>A, XM_047439285.1:c.154G>A, XM_047439290.1:c.154G>A, XM_047439265.1:c.154G>A, XM_047439269.1:c.154G>A, XM_047439288.1:c.154G>A, XM_047439274.1:c.154G>A, XM_047439260.1:c.154G>A, XM_047439262.1:c.154G>A, XM_047439280.1:c.154G>A, XM_047439277.1:c.154G>A, XM_047439287.1:c.154G>A, XM_047439283.1:c.154G>A, XM_047439259.1:c.154G>A, XM_047439278.1:c.154G>A, XM_047439289.1:c.154G>A, XM_047439284.1:c.154G>A, NP_003191.1:p.Asp52Asn, NP_001129611.1:p.Asp52Asn, NP_001338708.1:p.Asp52Asn, NP_001338707.1:p.Asp52Asn, XP_006722918.1:p.Asp52Asn, XP_011526528.1:p.Asp52Asn, XP_011526527.1:p.Asp52Asn, XP_016882670.1:p.Asp52Asn, XP_016882667.1:p.Asp52Asn, XP_047295226.1:p.Asp52Asn, XP_047295231.1:p.Asp52Asn, XP_047295219.1:p.Asp52Asn, XP_047295222.1:p.Asp52Asn, XP_047295228.1:p.Asp52Asn, XP_047295227.1:p.Asp52Asn, XP_047295220.1:p.Asp52Asn, XP_047295223.1:p.Asp52Asn, XP_047295224.1:p.Asp52Asn, XP_047295229.1:p.Asp52Asn, XP_047295232.1:p.Asp52Asn, XP_047295237.1:p.Asp52Asn, XP_047295214.1:p.Asp52Asn, XP_047295217.1:p.Asp52Asn, XP_047295235.1:p.Asp52Asn, XP_047295238.1:p.Asp52Asn, XP_047295247.1:p.Asp52Asn, XP_047295242.1:p.Asp52Asn, XP_047295241.1:p.Asp52Asn, XP_047295246.1:p.Asp52Asn, XP_047295221.1:p.Asp52Asn, XP_047295225.1:p.Asp52Asn, XP_047295244.1:p.Asp52Asn, XP_047295230.1:p.Asp52Asn, XP_047295216.1:p.Asp52Asn, XP_047295218.1:p.Asp52Asn, XP_047295236.1:p.Asp52Asn, XP_047295233.1:p.Asp52Asn, XP_047295243.1:p.Asp52Asn, XP_047295239.1:p.Asp52Asn, XP_047295215.1:p.Asp52Asn, XP_047295234.1:p.Asp52Asn, XP_047295245.1:p.Asp52Asn, XP_047295240.1:p.Asp52Asn

                8.

                rs1482804683 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A [Show Flanks]
                  Chromosome:
                  19:1627395 (GRCh38)
                  19:1627394 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:1627394:G:A
                  Gene:
                  TCF3 (Varview)
                  Functional Consequence:
                  synonymous_variant,coding_sequence_variant
                  Validated:
                  by frequency
                  MAF:
                  A=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000019.10:g.1627395G>A, NC_000019.9:g.1627394G>A, NG_029953.2:g.30152C>T, NM_003200.5:c.330C>T, NM_003200.4:c.330C>T, NM_003200.3:c.330C>T, NM_001136139.4:c.330C>T, NM_001136139.3:c.330C>T, NM_001136139.2:c.330C>T, NM_001351779.2:c.330C>T, NM_001351779.1:c.330C>T, NM_001351778.2:c.330C>T, NM_001351778.1:c.330C>T, XM_006722855.5:c.417C>T, XM_006722855.4:c.417C>T, XM_006722855.3:c.417C>T, XM_006722855.2:c.417C>T, XM_006722855.1:c.417C>T, XM_011528226.3:c.330C>T, XM_011528226.2:c.330C>T, XM_011528226.1:c.330C>T, XM_011528225.3:c.330C>T, XM_011528225.2:c.330C>T, XM_011528225.1:c.330C>T, XM_017027181.2:c.330C>T, XM_017027181.1:c.330C>T, XM_017027178.2:c.417C>T, XM_017027178.1:c.417C>T, XM_047439270.1:c.330C>T, XM_047439275.1:c.330C>T, XM_047439263.1:c.330C>T, XM_047439266.1:c.330C>T, XM_047439272.1:c.330C>T, XM_047439271.1:c.330C>T, XM_047439292.1:c.177C>T, XM_047439264.1:c.330C>T, XM_047439267.1:c.330C>T, XM_047439268.1:c.330C>T, XM_047439273.1:c.330C>T, XM_047439293.1:c.177C>T, XM_047439276.1:c.330C>T, XM_047439281.1:c.330C>T, XM_047439258.1:c.417C>T, XM_047439261.1:c.417C>T, XM_047439279.1:c.330C>T, XM_047439282.1:c.330C>T, XM_047439291.1:c.330C>T, XM_047439286.1:c.330C>T, XM_047439285.1:c.330C>T, XM_047439290.1:c.330C>T, XM_047439295.1:c.177C>T, XM_047439294.1:c.177C>T, XM_047439297.1:c.177C>T, XM_047439298.1:c.177C>T, XM_047439265.1:c.330C>T, XM_047439269.1:c.330C>T, XM_047439288.1:c.330C>T, XM_047439274.1:c.330C>T, XM_047439260.1:c.417C>T, XM_047439262.1:c.417C>T, XM_047439280.1:c.330C>T, XM_047439277.1:c.330C>T, XM_047439287.1:c.330C>T, XM_047439283.1:c.330C>T, XM_047439296.1:c.177C>T, XM_047439259.1:c.417C>T, XM_047439278.1:c.330C>T, XM_047439289.1:c.330C>T, XM_047439284.1:c.330C>T

                  9.

                  rs1482501016 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A,T [Show Flanks]
                    Chromosome:
                    19:1632115 (GRCh38)
                    19:1632114 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:1632114:G:A,NC_000019.10:1632114:G:T
                    Gene:
                    TCF3 (Varview)
                    Functional Consequence:
                    missense_variant,intron_variant,coding_sequence_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000007/1 (GnomAD)
                    HGVS:
                    NC_000019.10:g.1632115G>A, NC_000019.10:g.1632115G>T, NC_000019.9:g.1632114G>A, NC_000019.9:g.1632114G>T, NG_029953.2:g.25432C>T, NG_029953.2:g.25432C>A, NM_003200.5:c.221C>T, NM_003200.5:c.221C>A, NM_003200.4:c.221C>T, NM_003200.4:c.221C>A, NM_003200.3:c.221C>T, NM_003200.3:c.221C>A, NM_001136139.4:c.221C>T, NM_001136139.4:c.221C>A, NM_001136139.3:c.221C>T, NM_001136139.3:c.221C>A, NM_001136139.2:c.221C>T, NM_001136139.2:c.221C>A, NM_001351779.2:c.221C>T, NM_001351779.2:c.221C>A, NM_001351779.1:c.221C>T, NM_001351779.1:c.221C>A, NM_001351778.2:c.221C>T, NM_001351778.2:c.221C>A, NM_001351778.1:c.221C>T, NM_001351778.1:c.221C>A, XM_006722855.5:c.221C>T, XM_006722855.5:c.221C>A, XM_006722855.4:c.221C>T, XM_006722855.4:c.221C>A, XM_006722855.3:c.221C>T, XM_006722855.3:c.221C>A, XM_006722855.2:c.221C>T, XM_006722855.2:c.221C>A, XM_006722855.1:c.221C>T, XM_006722855.1:c.221C>A, XM_011528226.3:c.221C>T, XM_011528226.3:c.221C>A, XM_011528226.2:c.221C>T, XM_011528226.2:c.221C>A, XM_011528226.1:c.221C>T, XM_011528226.1:c.221C>A, XM_011528225.3:c.221C>T, XM_011528225.3:c.221C>A, XM_011528225.2:c.221C>T, XM_011528225.2:c.221C>A, XM_011528225.1:c.221C>T, XM_011528225.1:c.221C>A, XM_017027181.2:c.221C>T, XM_017027181.2:c.221C>A, XM_017027181.1:c.221C>T, XM_017027181.1:c.221C>A, XM_017027178.2:c.221C>T, XM_017027178.2:c.221C>A, XM_017027178.1:c.221C>T, XM_017027178.1:c.221C>A, XM_047439270.1:c.221C>T, XM_047439270.1:c.221C>A, XM_047439275.1:c.221C>T, XM_047439275.1:c.221C>A, XM_047439263.1:c.221C>T, XM_047439263.1:c.221C>A, XM_047439266.1:c.221C>T, XM_047439266.1:c.221C>A, XM_047439272.1:c.221C>T, XM_047439272.1:c.221C>A, XM_047439271.1:c.221C>T, XM_047439271.1:c.221C>A, XM_047439264.1:c.221C>T, XM_047439264.1:c.221C>A, XM_047439267.1:c.221C>T, XM_047439267.1:c.221C>A, XM_047439268.1:c.221C>T, XM_047439268.1:c.221C>A, XM_047439273.1:c.221C>T, XM_047439273.1:c.221C>A, XM_047439276.1:c.221C>T, XM_047439276.1:c.221C>A, XM_047439281.1:c.221C>T, XM_047439281.1:c.221C>A, XM_047439258.1:c.221C>T, XM_047439258.1:c.221C>A, XM_047439261.1:c.221C>T, XM_047439261.1:c.221C>A, XM_047439279.1:c.221C>T, XM_047439279.1:c.221C>A, XM_047439282.1:c.221C>T, XM_047439282.1:c.221C>A, XM_047439291.1:c.221C>T, XM_047439291.1:c.221C>A, XM_047439286.1:c.221C>T, XM_047439286.1:c.221C>A, XM_047439285.1:c.221C>T, XM_047439285.1:c.221C>A, XM_047439290.1:c.221C>T, XM_047439290.1:c.221C>A, XM_047439265.1:c.221C>T, XM_047439265.1:c.221C>A, XM_047439269.1:c.221C>T, XM_047439269.1:c.221C>A, XM_047439288.1:c.221C>T, XM_047439288.1:c.221C>A, XM_047439274.1:c.221C>T, XM_047439274.1:c.221C>A, XM_047439260.1:c.221C>T, XM_047439260.1:c.221C>A, XM_047439262.1:c.221C>T, XM_047439262.1:c.221C>A, XM_047439280.1:c.221C>T, XM_047439280.1:c.221C>A, XM_047439277.1:c.221C>T, XM_047439277.1:c.221C>A, XM_047439287.1:c.221C>T, XM_047439287.1:c.221C>A, XM_047439283.1:c.221C>T, XM_047439283.1:c.221C>A, XM_047439259.1:c.221C>T, XM_047439259.1:c.221C>A, XM_047439278.1:c.221C>T, XM_047439278.1:c.221C>A, XM_047439289.1:c.221C>T, XM_047439289.1:c.221C>A, XM_047439284.1:c.221C>T, XM_047439284.1:c.221C>A, NP_003191.1:p.Thr74Ile, NP_003191.1:p.Thr74Asn, NP_001129611.1:p.Thr74Ile, NP_001129611.1:p.Thr74Asn, NP_001338708.1:p.Thr74Ile, NP_001338708.1:p.Thr74Asn, NP_001338707.1:p.Thr74Ile, NP_001338707.1:p.Thr74Asn, XP_006722918.1:p.Thr74Ile, XP_006722918.1:p.Thr74Asn, XP_011526528.1:p.Thr74Ile, XP_011526528.1:p.Thr74Asn, XP_011526527.1:p.Thr74Ile, XP_011526527.1:p.Thr74Asn, XP_016882670.1:p.Thr74Ile, XP_016882670.1:p.Thr74Asn, XP_016882667.1:p.Thr74Ile, XP_016882667.1:p.Thr74Asn, XP_047295226.1:p.Thr74Ile, XP_047295226.1:p.Thr74Asn, XP_047295231.1:p.Thr74Ile, XP_047295231.1:p.Thr74Asn, XP_047295219.1:p.Thr74Ile, XP_047295219.1:p.Thr74Asn, XP_047295222.1:p.Thr74Ile, XP_047295222.1:p.Thr74Asn, XP_047295228.1:p.Thr74Ile, XP_047295228.1:p.Thr74Asn, XP_047295227.1:p.Thr74Ile, XP_047295227.1:p.Thr74Asn, XP_047295220.1:p.Thr74Ile, XP_047295220.1:p.Thr74Asn, XP_047295223.1:p.Thr74Ile, XP_047295223.1:p.Thr74Asn, XP_047295224.1:p.Thr74Ile, XP_047295224.1:p.Thr74Asn, XP_047295229.1:p.Thr74Ile, XP_047295229.1:p.Thr74Asn, XP_047295232.1:p.Thr74Ile, XP_047295232.1:p.Thr74Asn, XP_047295237.1:p.Thr74Ile, XP_047295237.1:p.Thr74Asn, XP_047295214.1:p.Thr74Ile, XP_047295214.1:p.Thr74Asn, XP_047295217.1:p.Thr74Ile, XP_047295217.1:p.Thr74Asn, XP_047295235.1:p.Thr74Ile, XP_047295235.1:p.Thr74Asn, XP_047295238.1:p.Thr74Ile, XP_047295238.1:p.Thr74Asn, XP_047295247.1:p.Thr74Ile, XP_047295247.1:p.Thr74Asn, XP_047295242.1:p.Thr74Ile, XP_047295242.1:p.Thr74Asn, XP_047295241.1:p.Thr74Ile, XP_047295241.1:p.Thr74Asn, XP_047295246.1:p.Thr74Ile, XP_047295246.1:p.Thr74Asn, XP_047295221.1:p.Thr74Ile, XP_047295221.1:p.Thr74Asn, XP_047295225.1:p.Thr74Ile, XP_047295225.1:p.Thr74Asn, XP_047295244.1:p.Thr74Ile, XP_047295244.1:p.Thr74Asn, XP_047295230.1:p.Thr74Ile, XP_047295230.1:p.Thr74Asn, XP_047295216.1:p.Thr74Ile, XP_047295216.1:p.Thr74Asn, XP_047295218.1:p.Thr74Ile, XP_047295218.1:p.Thr74Asn, XP_047295236.1:p.Thr74Ile, XP_047295236.1:p.Thr74Asn, XP_047295233.1:p.Thr74Ile, XP_047295233.1:p.Thr74Asn, XP_047295243.1:p.Thr74Ile, XP_047295243.1:p.Thr74Asn, XP_047295239.1:p.Thr74Ile, XP_047295239.1:p.Thr74Asn, XP_047295215.1:p.Thr74Ile, XP_047295215.1:p.Thr74Asn, XP_047295234.1:p.Thr74Ile, XP_047295234.1:p.Thr74Asn, XP_047295245.1:p.Thr74Ile, XP_047295245.1:p.Thr74Asn, XP_047295240.1:p.Thr74Ile, XP_047295240.1:p.Thr74Asn

                    10.

                    rs1482491713 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>G [Show Flanks]
                      Chromosome:
                      19:1619321 (GRCh38)
                      19:1619320 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:1619320:C:G
                      Gene:
                      TCF3 (Varview)
                      Functional Consequence:
                      missense_variant,coding_sequence_variant
                      Validated:
                      by frequency
                      MAF:
                      G=0.000005/1 (GnomAD_exomes)
                      HGVS:
                      NC_000019.10:g.1619321C>G, NC_000019.9:g.1619320C>G, NG_029953.2:g.38226G>C, NM_003200.5:c.1321G>C, NM_003200.4:c.1321G>C, NM_003200.3:c.1321G>C, NM_001136139.4:c.1321G>C, NM_001136139.3:c.1321G>C, NM_001136139.2:c.1321G>C, NM_001351779.2:c.1321G>C, NM_001351779.1:c.1321G>C, NM_001351778.2:c.1318G>C, NM_001351778.1:c.1318G>C, XM_006722855.5:c.1408G>C, XM_006722855.4:c.1408G>C, XM_006722855.3:c.1408G>C, XM_006722855.2:c.1408G>C, XM_006722855.1:c.1408G>C, XM_011528226.3:c.1318G>C, XM_011528226.2:c.1318G>C, XM_011528226.1:c.1318G>C, XM_011528225.3:c.1321G>C, XM_011528225.2:c.1321G>C, XM_011528225.1:c.1321G>C, XM_017027181.2:c.1321G>C, XM_017027181.1:c.1321G>C, XM_017027178.2:c.1408G>C, XM_017027178.1:c.1408G>C, XM_047439270.1:c.1321G>C, XM_047439275.1:c.1318G>C, XM_047439263.1:c.1321G>C, XM_047439266.1:c.1318G>C, XM_047439272.1:c.1321G>C, XM_047439271.1:c.1318G>C, XM_047439292.1:c.1168G>C, XM_047439264.1:c.1321G>C, XM_047439267.1:c.1318G>C, XM_047439268.1:c.1321G>C, XM_047439273.1:c.1318G>C, XM_047439293.1:c.1168G>C, XM_047439276.1:c.1321G>C, XM_047439281.1:c.1321G>C, XM_047439258.1:c.1408G>C, XM_047439261.1:c.1405G>C, XM_047439279.1:c.1318G>C, XM_047439282.1:c.1321G>C, XM_047439291.1:c.1318G>C, XM_047439286.1:c.1318G>C, XM_047439285.1:c.1321G>C, XM_047439290.1:c.1318G>C, XM_047439295.1:c.1168G>C, XM_047439294.1:c.1168G>C, XM_047439297.1:c.1168G>C, XM_047439298.1:c.1168G>C, XM_047439265.1:c.1321G>C, XM_047439269.1:c.1321G>C, XM_047439288.1:c.1321G>C, XM_047439274.1:c.1318G>C, XM_047439260.1:c.1408G>C, XM_047439262.1:c.1408G>C, XM_047439280.1:c.1318G>C, XM_047439277.1:c.1321G>C, XM_047439287.1:c.1321G>C, XM_047439283.1:c.1321G>C, XM_047439296.1:c.1168G>C, XM_047439259.1:c.1408G>C, XM_047439278.1:c.1321G>C, XM_047439289.1:c.1321G>C, XM_047439284.1:c.1321G>C, NP_003191.1:p.Gly441Arg, NP_001129611.1:p.Gly441Arg, NP_001338708.1:p.Gly441Arg, NP_001338707.1:p.Gly440Arg, XP_006722918.1:p.Gly470Arg, XP_011526528.1:p.Gly440Arg, XP_011526527.1:p.Gly441Arg, XP_016882670.1:p.Gly441Arg, XP_016882667.1:p.Gly470Arg, XP_047295226.1:p.Gly441Arg, XP_047295231.1:p.Gly440Arg, XP_047295219.1:p.Gly441Arg, XP_047295222.1:p.Gly440Arg, XP_047295228.1:p.Gly441Arg, XP_047295227.1:p.Gly440Arg, XP_047295248.1:p.Gly390Arg, XP_047295220.1:p.Gly441Arg, XP_047295223.1:p.Gly440Arg, XP_047295224.1:p.Gly441Arg, XP_047295229.1:p.Gly440Arg, XP_047295249.1:p.Gly390Arg, XP_047295232.1:p.Gly441Arg, XP_047295237.1:p.Gly441Arg, XP_047295214.1:p.Gly470Arg, XP_047295217.1:p.Gly469Arg, XP_047295235.1:p.Gly440Arg, XP_047295238.1:p.Gly441Arg, XP_047295247.1:p.Gly440Arg, XP_047295242.1:p.Gly440Arg, XP_047295241.1:p.Gly441Arg, XP_047295246.1:p.Gly440Arg, XP_047295251.1:p.Gly390Arg, XP_047295250.1:p.Gly390Arg, XP_047295253.1:p.Gly390Arg, XP_047295254.1:p.Gly390Arg, XP_047295221.1:p.Gly441Arg, XP_047295225.1:p.Gly441Arg, XP_047295244.1:p.Gly441Arg, XP_047295230.1:p.Gly440Arg, XP_047295216.1:p.Gly470Arg, XP_047295218.1:p.Gly470Arg, XP_047295236.1:p.Gly440Arg, XP_047295233.1:p.Gly441Arg, XP_047295243.1:p.Gly441Arg, XP_047295239.1:p.Gly441Arg, XP_047295252.1:p.Gly390Arg, XP_047295215.1:p.Gly470Arg, XP_047295234.1:p.Gly441Arg, XP_047295245.1:p.Gly441Arg, XP_047295240.1:p.Gly441Arg

                      11.

                      rs1481888878 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        19:1622381 (GRCh38)
                        19:1622380 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:1622380:C:T
                        Gene:
                        TCF3 (Varview)
                        Functional Consequence:
                        missense_variant,coding_sequence_variant
                        Validated:
                        by frequency,by cluster
                        MAF:
                        T=0.000007/1 (GnomAD)
                        T=0.000223/1 (Estonian)
                        HGVS:
                        NC_000019.10:g.1622381C>T, NC_000019.9:g.1622380C>T, NG_029953.2:g.35166G>A, NM_003200.5:c.584G>A, NM_003200.4:c.584G>A, NM_003200.3:c.584G>A, NM_001136139.4:c.584G>A, NM_001136139.3:c.584G>A, NM_001136139.2:c.584G>A, NM_001351779.2:c.584G>A, NM_001351779.1:c.584G>A, NM_001351778.2:c.584G>A, NM_001351778.1:c.584G>A, XM_006722855.5:c.671G>A, XM_006722855.4:c.671G>A, XM_006722855.3:c.671G>A, XM_006722855.2:c.671G>A, XM_006722855.1:c.671G>A, XM_011528226.3:c.584G>A, XM_011528226.2:c.584G>A, XM_011528226.1:c.584G>A, XM_011528225.3:c.584G>A, XM_011528225.2:c.584G>A, XM_011528225.1:c.584G>A, XM_017027181.2:c.584G>A, XM_017027181.1:c.584G>A, XM_017027178.2:c.671G>A, XM_017027178.1:c.671G>A, XM_047439270.1:c.584G>A, XM_047439275.1:c.584G>A, XM_047439263.1:c.584G>A, XM_047439266.1:c.584G>A, XM_047439272.1:c.584G>A, XM_047439271.1:c.584G>A, XM_047439292.1:c.431G>A, XM_047439264.1:c.584G>A, XM_047439267.1:c.584G>A, XM_047439268.1:c.584G>A, XM_047439273.1:c.584G>A, XM_047439293.1:c.431G>A, XM_047439276.1:c.584G>A, XM_047439281.1:c.584G>A, XM_047439258.1:c.671G>A, XM_047439261.1:c.671G>A, XM_047439279.1:c.584G>A, XM_047439282.1:c.584G>A, XM_047439291.1:c.584G>A, XM_047439286.1:c.584G>A, XM_047439285.1:c.584G>A, XM_047439290.1:c.584G>A, XM_047439295.1:c.431G>A, XM_047439294.1:c.431G>A, XM_047439297.1:c.431G>A, XM_047439298.1:c.431G>A, XM_047439265.1:c.584G>A, XM_047439269.1:c.584G>A, XM_047439288.1:c.584G>A, XM_047439274.1:c.584G>A, XM_047439260.1:c.671G>A, XM_047439262.1:c.671G>A, XM_047439280.1:c.584G>A, XM_047439277.1:c.584G>A, XM_047439287.1:c.584G>A, XM_047439283.1:c.584G>A, XM_047439296.1:c.431G>A, XM_047439259.1:c.671G>A, XM_047439278.1:c.584G>A, XM_047439289.1:c.584G>A, XM_047439284.1:c.584G>A, NP_003191.1:p.Arg195Lys, NP_001129611.1:p.Arg195Lys, NP_001338708.1:p.Arg195Lys, NP_001338707.1:p.Arg195Lys, XP_006722918.1:p.Arg224Lys, XP_011526528.1:p.Arg195Lys, XP_011526527.1:p.Arg195Lys, XP_016882670.1:p.Arg195Lys, XP_016882667.1:p.Arg224Lys, XP_047295226.1:p.Arg195Lys, XP_047295231.1:p.Arg195Lys, XP_047295219.1:p.Arg195Lys, XP_047295222.1:p.Arg195Lys, XP_047295228.1:p.Arg195Lys, XP_047295227.1:p.Arg195Lys, XP_047295248.1:p.Arg144Lys, XP_047295220.1:p.Arg195Lys, XP_047295223.1:p.Arg195Lys, XP_047295224.1:p.Arg195Lys, XP_047295229.1:p.Arg195Lys, XP_047295249.1:p.Arg144Lys, XP_047295232.1:p.Arg195Lys, XP_047295237.1:p.Arg195Lys, XP_047295214.1:p.Arg224Lys, XP_047295217.1:p.Arg224Lys, XP_047295235.1:p.Arg195Lys, XP_047295238.1:p.Arg195Lys, XP_047295247.1:p.Arg195Lys, XP_047295242.1:p.Arg195Lys, XP_047295241.1:p.Arg195Lys, XP_047295246.1:p.Arg195Lys, XP_047295251.1:p.Arg144Lys, XP_047295250.1:p.Arg144Lys, XP_047295253.1:p.Arg144Lys, XP_047295254.1:p.Arg144Lys, XP_047295221.1:p.Arg195Lys, XP_047295225.1:p.Arg195Lys, XP_047295244.1:p.Arg195Lys, XP_047295230.1:p.Arg195Lys, XP_047295216.1:p.Arg224Lys, XP_047295218.1:p.Arg224Lys, XP_047295236.1:p.Arg195Lys, XP_047295233.1:p.Arg195Lys, XP_047295243.1:p.Arg195Lys, XP_047295239.1:p.Arg195Lys, XP_047295252.1:p.Arg144Lys, XP_047295215.1:p.Arg224Lys, XP_047295234.1:p.Arg195Lys, XP_047295245.1:p.Arg195Lys, XP_047295240.1:p.Arg195Lys

                        12.

                        rs1481750909 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C [Show Flanks]
                          Chromosome:
                          19:1619824 (GRCh38)
                          19:1619823 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:1619823:G:A,NC_000019.10:1619823:G:C
                          Gene:
                          TCF3 (Varview)
                          Functional Consequence:
                          missense_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          HGVS:
                          NC_000019.10:g.1619824G>A, NC_000019.10:g.1619824G>C, NC_000019.9:g.1619823G>A, NC_000019.9:g.1619823G>C, NG_029953.2:g.37723C>T, NG_029953.2:g.37723C>G, NM_003200.5:c.1123C>T, NM_003200.5:c.1123C>G, NM_003200.4:c.1123C>T, NM_003200.4:c.1123C>G, NM_003200.3:c.1123C>T, NM_003200.3:c.1123C>G, NM_001136139.4:c.1123C>T, NM_001136139.4:c.1123C>G, NM_001136139.3:c.1123C>T, NM_001136139.3:c.1123C>G, NM_001136139.2:c.1123C>T, NM_001136139.2:c.1123C>G, NM_001351779.2:c.1123C>T, NM_001351779.2:c.1123C>G, NM_001351779.1:c.1123C>T, NM_001351779.1:c.1123C>G, NM_001351778.2:c.1123C>T, NM_001351778.2:c.1123C>G, NM_001351778.1:c.1123C>T, NM_001351778.1:c.1123C>G, XM_006722855.5:c.1210C>T, XM_006722855.5:c.1210C>G, XM_006722855.4:c.1210C>T, XM_006722855.4:c.1210C>G, XM_006722855.3:c.1210C>T, XM_006722855.3:c.1210C>G, XM_006722855.2:c.1210C>T, XM_006722855.2:c.1210C>G, XM_006722855.1:c.1210C>T, XM_006722855.1:c.1210C>G, XM_011528226.3:c.1123C>T, XM_011528226.3:c.1123C>G, XM_011528226.2:c.1123C>T, XM_011528226.2:c.1123C>G, XM_011528226.1:c.1123C>T, XM_011528226.1:c.1123C>G, XM_011528225.3:c.1123C>T, XM_011528225.3:c.1123C>G, XM_011528225.2:c.1123C>T, XM_011528225.2:c.1123C>G, XM_011528225.1:c.1123C>T, XM_011528225.1:c.1123C>G, XM_017027181.2:c.1123C>T, XM_017027181.2:c.1123C>G, XM_017027181.1:c.1123C>T, XM_017027181.1:c.1123C>G, XM_017027178.2:c.1210C>T, XM_017027178.2:c.1210C>G, XM_017027178.1:c.1210C>T, XM_017027178.1:c.1210C>G, XM_047439270.1:c.1123C>T, XM_047439270.1:c.1123C>G, XM_047439275.1:c.1123C>T, XM_047439275.1:c.1123C>G, XM_047439263.1:c.1123C>T, XM_047439263.1:c.1123C>G, XM_047439266.1:c.1123C>T, XM_047439266.1:c.1123C>G, XM_047439272.1:c.1123C>T, XM_047439272.1:c.1123C>G, XM_047439271.1:c.1123C>T, XM_047439271.1:c.1123C>G, XM_047439292.1:c.970C>T, XM_047439292.1:c.970C>G, XM_047439264.1:c.1123C>T, XM_047439264.1:c.1123C>G, XM_047439267.1:c.1123C>T, XM_047439267.1:c.1123C>G, XM_047439268.1:c.1123C>T, XM_047439268.1:c.1123C>G, XM_047439273.1:c.1123C>T, XM_047439273.1:c.1123C>G, XM_047439293.1:c.970C>T, XM_047439293.1:c.970C>G, XM_047439276.1:c.1123C>T, XM_047439276.1:c.1123C>G, XM_047439281.1:c.1123C>T, XM_047439281.1:c.1123C>G, XM_047439258.1:c.1210C>T, XM_047439258.1:c.1210C>G, XM_047439261.1:c.1210C>T, XM_047439261.1:c.1210C>G, XM_047439279.1:c.1123C>T, XM_047439279.1:c.1123C>G, XM_047439282.1:c.1123C>T, XM_047439282.1:c.1123C>G, XM_047439291.1:c.1123C>T, XM_047439291.1:c.1123C>G, XM_047439286.1:c.1123C>T, XM_047439286.1:c.1123C>G, XM_047439285.1:c.1123C>T, XM_047439285.1:c.1123C>G, XM_047439290.1:c.1123C>T, XM_047439290.1:c.1123C>G, XM_047439295.1:c.970C>T, XM_047439295.1:c.970C>G, XM_047439294.1:c.970C>T, XM_047439294.1:c.970C>G, XM_047439297.1:c.970C>T, XM_047439297.1:c.970C>G, XM_047439298.1:c.970C>T, XM_047439298.1:c.970C>G, XM_047439265.1:c.1123C>T, XM_047439265.1:c.1123C>G, XM_047439269.1:c.1123C>T, XM_047439269.1:c.1123C>G, XM_047439288.1:c.1123C>T, XM_047439288.1:c.1123C>G, XM_047439274.1:c.1123C>T, XM_047439274.1:c.1123C>G, XM_047439260.1:c.1210C>T, XM_047439260.1:c.1210C>G, XM_047439262.1:c.1210C>T, XM_047439262.1:c.1210C>G, XM_047439280.1:c.1123C>T, XM_047439280.1:c.1123C>G, XM_047439277.1:c.1123C>T, XM_047439277.1:c.1123C>G, XM_047439287.1:c.1123C>T, XM_047439287.1:c.1123C>G, XM_047439283.1:c.1123C>T, XM_047439283.1:c.1123C>G, XM_047439296.1:c.970C>T, XM_047439296.1:c.970C>G, XM_047439259.1:c.1210C>T, XM_047439259.1:c.1210C>G, XM_047439278.1:c.1123C>T, XM_047439278.1:c.1123C>G, XM_047439289.1:c.1123C>T, XM_047439289.1:c.1123C>G, XM_047439284.1:c.1123C>T, XM_047439284.1:c.1123C>G, NP_003191.1:p.Pro375Ser, NP_003191.1:p.Pro375Ala, NP_001129611.1:p.Pro375Ser, NP_001129611.1:p.Pro375Ala, NP_001338708.1:p.Pro375Ser, NP_001338708.1:p.Pro375Ala, NP_001338707.1:p.Pro375Ser, NP_001338707.1:p.Pro375Ala, XP_006722918.1:p.Pro404Ser, XP_006722918.1:p.Pro404Ala, XP_011526528.1:p.Pro375Ser, XP_011526528.1:p.Pro375Ala, XP_011526527.1:p.Pro375Ser, XP_011526527.1:p.Pro375Ala, XP_016882670.1:p.Pro375Ser, XP_016882670.1:p.Pro375Ala, XP_016882667.1:p.Pro404Ser, XP_016882667.1:p.Pro404Ala, XP_047295226.1:p.Pro375Ser, XP_047295226.1:p.Pro375Ala, XP_047295231.1:p.Pro375Ser, XP_047295231.1:p.Pro375Ala, XP_047295219.1:p.Pro375Ser, XP_047295219.1:p.Pro375Ala, XP_047295222.1:p.Pro375Ser, XP_047295222.1:p.Pro375Ala, XP_047295228.1:p.Pro375Ser, XP_047295228.1:p.Pro375Ala, XP_047295227.1:p.Pro375Ser, XP_047295227.1:p.Pro375Ala, XP_047295248.1:p.Pro324Ser, XP_047295248.1:p.Pro324Ala, XP_047295220.1:p.Pro375Ser, XP_047295220.1:p.Pro375Ala, XP_047295223.1:p.Pro375Ser, XP_047295223.1:p.Pro375Ala, XP_047295224.1:p.Pro375Ser, XP_047295224.1:p.Pro375Ala, XP_047295229.1:p.Pro375Ser, XP_047295229.1:p.Pro375Ala, XP_047295249.1:p.Pro324Ser, XP_047295249.1:p.Pro324Ala, XP_047295232.1:p.Pro375Ser, XP_047295232.1:p.Pro375Ala, XP_047295237.1:p.Pro375Ser, XP_047295237.1:p.Pro375Ala, XP_047295214.1:p.Pro404Ser, XP_047295214.1:p.Pro404Ala, XP_047295217.1:p.Pro404Ser, XP_047295217.1:p.Pro404Ala, XP_047295235.1:p.Pro375Ser, XP_047295235.1:p.Pro375Ala, XP_047295238.1:p.Pro375Ser, XP_047295238.1:p.Pro375Ala, XP_047295247.1:p.Pro375Ser, XP_047295247.1:p.Pro375Ala, XP_047295242.1:p.Pro375Ser, XP_047295242.1:p.Pro375Ala, XP_047295241.1:p.Pro375Ser, XP_047295241.1:p.Pro375Ala, XP_047295246.1:p.Pro375Ser, XP_047295246.1:p.Pro375Ala, XP_047295251.1:p.Pro324Ser, XP_047295251.1:p.Pro324Ala, XP_047295250.1:p.Pro324Ser, XP_047295250.1:p.Pro324Ala, XP_047295253.1:p.Pro324Ser, XP_047295253.1:p.Pro324Ala, XP_047295254.1:p.Pro324Ser, XP_047295254.1:p.Pro324Ala, XP_047295221.1:p.Pro375Ser, XP_047295221.1:p.Pro375Ala, XP_047295225.1:p.Pro375Ser, XP_047295225.1:p.Pro375Ala, XP_047295244.1:p.Pro375Ser, XP_047295244.1:p.Pro375Ala, XP_047295230.1:p.Pro375Ser, XP_047295230.1:p.Pro375Ala, XP_047295216.1:p.Pro404Ser, XP_047295216.1:p.Pro404Ala, XP_047295218.1:p.Pro404Ser, XP_047295218.1:p.Pro404Ala, XP_047295236.1:p.Pro375Ser, XP_047295236.1:p.Pro375Ala, XP_047295233.1:p.Pro375Ser, XP_047295233.1:p.Pro375Ala, XP_047295243.1:p.Pro375Ser, XP_047295243.1:p.Pro375Ala, XP_047295239.1:p.Pro375Ser, XP_047295239.1:p.Pro375Ala, XP_047295252.1:p.Pro324Ser, XP_047295252.1:p.Pro324Ala, XP_047295215.1:p.Pro404Ser, XP_047295215.1:p.Pro404Ala, XP_047295234.1:p.Pro375Ser, XP_047295234.1:p.Pro375Ala, XP_047295245.1:p.Pro375Ser, XP_047295245.1:p.Pro375Ala, XP_047295240.1:p.Pro375Ser, XP_047295240.1:p.Pro375Ala

                          13.

                          rs1480818612 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G [Show Flanks]
                            Chromosome:
                            19:1619356 (GRCh38)
                            19:1619355 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:1619355:A:G
                            Gene:
                            TCF3 (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_variant
                            HGVS:
                            NC_000019.10:g.1619356A>G, NC_000019.9:g.1619355A>G, NG_029953.2:g.38191T>C, NM_003200.5:c.1286T>C, NM_003200.4:c.1286T>C, NM_003200.3:c.1286T>C, NM_001136139.4:c.1286T>C, NM_001136139.3:c.1286T>C, NM_001136139.2:c.1286T>C, NM_001351779.2:c.1286T>C, NM_001351779.1:c.1286T>C, NM_001351778.2:c.1283T>C, NM_001351778.1:c.1283T>C, XM_006722855.5:c.1373T>C, XM_006722855.4:c.1373T>C, XM_006722855.3:c.1373T>C, XM_006722855.2:c.1373T>C, XM_006722855.1:c.1373T>C, XM_011528226.3:c.1283T>C, XM_011528226.2:c.1283T>C, XM_011528226.1:c.1283T>C, XM_011528225.3:c.1286T>C, XM_011528225.2:c.1286T>C, XM_011528225.1:c.1286T>C, XM_017027181.2:c.1286T>C, XM_017027181.1:c.1286T>C, XM_017027178.2:c.1373T>C, XM_017027178.1:c.1373T>C, XM_047439270.1:c.1286T>C, XM_047439275.1:c.1283T>C, XM_047439263.1:c.1286T>C, XM_047439266.1:c.1283T>C, XM_047439272.1:c.1286T>C, XM_047439271.1:c.1283T>C, XM_047439292.1:c.1133T>C, XM_047439264.1:c.1286T>C, XM_047439267.1:c.1283T>C, XM_047439268.1:c.1286T>C, XM_047439273.1:c.1283T>C, XM_047439293.1:c.1133T>C, XM_047439276.1:c.1286T>C, XM_047439281.1:c.1286T>C, XM_047439258.1:c.1373T>C, XM_047439261.1:c.1370T>C, XM_047439279.1:c.1283T>C, XM_047439282.1:c.1286T>C, XM_047439291.1:c.1283T>C, XM_047439286.1:c.1283T>C, XM_047439285.1:c.1286T>C, XM_047439290.1:c.1283T>C, XM_047439295.1:c.1133T>C, XM_047439294.1:c.1133T>C, XM_047439297.1:c.1133T>C, XM_047439298.1:c.1133T>C, XM_047439265.1:c.1286T>C, XM_047439269.1:c.1286T>C, XM_047439288.1:c.1286T>C, XM_047439274.1:c.1283T>C, XM_047439260.1:c.1373T>C, XM_047439262.1:c.1373T>C, XM_047439280.1:c.1283T>C, XM_047439277.1:c.1286T>C, XM_047439287.1:c.1286T>C, XM_047439283.1:c.1286T>C, XM_047439296.1:c.1133T>C, XM_047439259.1:c.1373T>C, XM_047439278.1:c.1286T>C, XM_047439289.1:c.1286T>C, XM_047439284.1:c.1286T>C, NP_003191.1:p.Phe429Ser, NP_001129611.1:p.Phe429Ser, NP_001338708.1:p.Phe429Ser, NP_001338707.1:p.Phe428Ser, XP_006722918.1:p.Phe458Ser, XP_011526528.1:p.Phe428Ser, XP_011526527.1:p.Phe429Ser, XP_016882670.1:p.Phe429Ser, XP_016882667.1:p.Phe458Ser, XP_047295226.1:p.Phe429Ser, XP_047295231.1:p.Phe428Ser, XP_047295219.1:p.Phe429Ser, XP_047295222.1:p.Phe428Ser, XP_047295228.1:p.Phe429Ser, XP_047295227.1:p.Phe428Ser, XP_047295248.1:p.Phe378Ser, XP_047295220.1:p.Phe429Ser, XP_047295223.1:p.Phe428Ser, XP_047295224.1:p.Phe429Ser, XP_047295229.1:p.Phe428Ser, XP_047295249.1:p.Phe378Ser, XP_047295232.1:p.Phe429Ser, XP_047295237.1:p.Phe429Ser, XP_047295214.1:p.Phe458Ser, XP_047295217.1:p.Phe457Ser, XP_047295235.1:p.Phe428Ser, XP_047295238.1:p.Phe429Ser, XP_047295247.1:p.Phe428Ser, XP_047295242.1:p.Phe428Ser, XP_047295241.1:p.Phe429Ser, XP_047295246.1:p.Phe428Ser, XP_047295251.1:p.Phe378Ser, XP_047295250.1:p.Phe378Ser, XP_047295253.1:p.Phe378Ser, XP_047295254.1:p.Phe378Ser, XP_047295221.1:p.Phe429Ser, XP_047295225.1:p.Phe429Ser, XP_047295244.1:p.Phe429Ser, XP_047295230.1:p.Phe428Ser, XP_047295216.1:p.Phe458Ser, XP_047295218.1:p.Phe458Ser, XP_047295236.1:p.Phe428Ser, XP_047295233.1:p.Phe429Ser, XP_047295243.1:p.Phe429Ser, XP_047295239.1:p.Phe429Ser, XP_047295252.1:p.Phe378Ser, XP_047295215.1:p.Phe458Ser, XP_047295234.1:p.Phe429Ser, XP_047295245.1:p.Phe429Ser, XP_047295240.1:p.Phe429Ser

                            14.

                            rs1479468590 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              19:1611830 (GRCh38)
                              19:1611829 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:1611829:T:C
                              Gene:
                              TCF3 (Varview)
                              Functional Consequence:
                              synonymous_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0.000071/1 (ALFA)
                              C=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000019.10:g.1611830T>C, NC_000019.9:g.1611829T>C, NG_029953.2:g.45717A>G, NM_003200.5:c.1842A>G, NM_003200.4:c.1842A>G, NM_003200.3:c.1842A>G, NM_001136139.4:c.1833A>G, NM_001136139.3:c.1833A>G, NM_001136139.2:c.1833A>G, NM_001351779.2:c.1833A>G, NM_001351779.1:c.1833A>G, NM_001351778.2:c.1839A>G, NM_001351778.1:c.1839A>G, XM_006722855.5:c.1920A>G, XM_006722855.4:c.1920A>G, XM_006722855.3:c.1920A>G, XM_006722855.2:c.1920A>G, XM_006722855.1:c.1920A>G, XM_011528226.3:c.1830A>G, XM_011528226.2:c.1830A>G, XM_011528226.1:c.1830A>G, XM_011528225.3:c.1830A>G, XM_011528225.2:c.1830A>G, XM_011528225.1:c.1830A>G, XM_017027181.2:c.1842A>G, XM_017027181.1:c.1842A>G, XM_017027178.2:c.1920A>G, XM_017027178.1:c.1920A>G, XM_047439270.1:c.1830A>G, XM_047439275.1:c.1827A>G, XM_047439263.1:c.1842A>G, XM_047439266.1:c.1839A>G, XM_047439272.1:c.1830A>G, XM_047439271.1:c.1830A>G, XM_047439292.1:c.1680A>G, XM_047439264.1:c.1842A>G, XM_047439267.1:c.1839A>G, XM_047439268.1:c.1833A>G, XM_047439273.1:c.1830A>G, XM_047439293.1:c.1680A>G, XM_047439276.1:c.1842A>G, XM_047439281.1:c.1833A>G, XM_047439258.1:c.1929A>G, XM_047439261.1:c.1926A>G, XM_047439279.1:c.1839A>G, XM_047439282.1:c.1833A>G, XM_047439291.1:c.1827A>G, XM_047439286.1:c.1830A>G, XM_047439285.1:c.1830A>G, XM_047439290.1:c.1827A>G, XM_047439295.1:c.1689A>G, XM_047439294.1:c.1689A>G, XM_047439297.1:c.1680A>G, XM_047439298.1:c.1677A>G, XM_047439265.1:c.1842A>G, XM_047439269.1:c.1833A>G, XM_047439288.1:c.1830A>G, XM_047439274.1:c.1830A>G, XM_047439260.1:c.1929A>G, XM_047439262.1:c.1920A>G, XM_047439280.1:c.1839A>G, XM_047439277.1:c.1842A>G, XM_047439287.1:c.1830A>G, XM_047439283.1:c.1833A>G, XM_047439296.1:c.1689A>G, XM_047439259.1:c.1929A>G, XM_047439278.1:c.1842A>G, XM_047439289.1:c.1830A>G, XM_047439284.1:c.1833A>G

                              15.

                              rs1478702378 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                19:1650234 (GRCh38)
                                19:1650233 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:1650233:C:T
                                Gene:
                                TCF3 (Varview)
                                Functional Consequence:
                                synonymous_variant,coding_sequence_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                T=0.000006/1 (GnomAD_exomes)
                                T=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000019.10:g.1650234C>T, NC_000019.9:g.1650233C>T, NG_029953.2:g.7313G>A, NM_003200.5:c.15G>A, NM_003200.4:c.15G>A, NM_003200.3:c.15G>A, NM_001136139.4:c.15G>A, NM_001136139.3:c.15G>A, NM_001136139.2:c.15G>A, NM_001351779.2:c.15G>A, NM_001351779.1:c.15G>A, NM_001351778.2:c.15G>A, NM_001351778.1:c.15G>A, XM_006722855.5:c.15G>A, XM_006722855.4:c.15G>A, XM_006722855.3:c.15G>A, XM_006722855.2:c.15G>A, XM_006722855.1:c.15G>A, XM_011528226.3:c.15G>A, XM_011528226.2:c.15G>A, XM_011528226.1:c.15G>A, XM_011528225.3:c.15G>A, XM_011528225.2:c.15G>A, XM_011528225.1:c.15G>A, XM_017027181.2:c.15G>A, XM_017027181.1:c.15G>A, XM_017027178.2:c.15G>A, XM_017027178.1:c.15G>A, XM_047439270.1:c.15G>A, XM_047439275.1:c.15G>A, XM_047439263.1:c.15G>A, XM_047439266.1:c.15G>A, XM_047439272.1:c.15G>A, XM_047439271.1:c.15G>A, XM_047439292.1:c.15G>A, XM_047439264.1:c.15G>A, XM_047439267.1:c.15G>A, XM_047439268.1:c.15G>A, XM_047439273.1:c.15G>A, XM_047439293.1:c.15G>A, XM_047439276.1:c.15G>A, XM_047439281.1:c.15G>A, XM_047439258.1:c.15G>A, XM_047439261.1:c.15G>A, XM_047439279.1:c.15G>A, XM_047439282.1:c.15G>A, XM_047439291.1:c.15G>A, XM_047439286.1:c.15G>A, XM_047439285.1:c.15G>A, XM_047439290.1:c.15G>A, XM_047439295.1:c.15G>A, XM_047439294.1:c.15G>A, XM_047439297.1:c.15G>A, XM_047439298.1:c.15G>A, XM_047439265.1:c.15G>A, XM_047439269.1:c.15G>A, XM_047439288.1:c.15G>A, XM_047439274.1:c.15G>A, XM_047439260.1:c.15G>A, XM_047439262.1:c.15G>A, XM_047439280.1:c.15G>A, XM_047439277.1:c.15G>A, XM_047439287.1:c.15G>A, XM_047439283.1:c.15G>A, XM_047439296.1:c.15G>A, XM_047439259.1:c.15G>A, XM_047439278.1:c.15G>A, XM_047439289.1:c.15G>A, XM_047439284.1:c.15G>A

                                16.

                                rs1477839118 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  19:1612341 (GRCh38)
                                  19:1612340 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:1612340:C:T
                                  Gene:
                                  TCF3 (Varview)
                                  Functional Consequence:
                                  missense_variant,intron_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  T=0.000008/2 (GnomAD_exomes)
                                  HGVS:
                                  NC_000019.10:g.1612341C>T, NC_000019.9:g.1612340C>T, NG_029953.2:g.45206G>A, NM_001136139.4:c.1679G>A, NM_001136139.3:c.1679G>A, NM_001136139.2:c.1679G>A, NM_001351779.2:c.1679G>A, NM_001351779.1:c.1679G>A, XM_006722855.5:c.1766G>A, XM_006722855.4:c.1766G>A, XM_006722855.3:c.1766G>A, XM_006722855.2:c.1766G>A, XM_006722855.1:c.1766G>A, XM_011528226.3:c.1676G>A, XM_011528226.2:c.1676G>A, XM_011528226.1:c.1676G>A, XM_011528225.3:c.1676G>A, XM_011528225.2:c.1676G>A, XM_011528225.1:c.1676G>A, XM_017027178.2:c.1766G>A, XM_017027178.1:c.1766G>A, XM_047439270.1:c.1676G>A, XM_047439275.1:c.1673G>A, XM_047439272.1:c.1676G>A, XM_047439271.1:c.1676G>A, XM_047439292.1:c.1526G>A, XM_047439268.1:c.1679G>A, XM_047439273.1:c.1676G>A, XM_047439293.1:c.1526G>A, XM_047439281.1:c.1679G>A, XM_047439282.1:c.1679G>A, XM_047439291.1:c.1673G>A, XM_047439286.1:c.1676G>A, XM_047439285.1:c.1676G>A, XM_047439290.1:c.1673G>A, XM_047439297.1:c.1526G>A, XM_047439298.1:c.1523G>A, XM_047439269.1:c.1679G>A, XM_047439288.1:c.1676G>A, XM_047439274.1:c.1676G>A, XM_047439262.1:c.1766G>A, XM_047439287.1:c.1676G>A, XM_047439283.1:c.1679G>A, XM_047439289.1:c.1676G>A, XM_047439284.1:c.1679G>A, NP_001129611.1:p.Arg560Gln, NP_001338708.1:p.Arg560Gln, XP_006722918.1:p.Arg589Gln, XP_011526528.1:p.Arg559Gln, XP_011526527.1:p.Arg559Gln, XP_016882667.1:p.Arg589Gln, XP_047295226.1:p.Arg559Gln, XP_047295231.1:p.Arg558Gln, XP_047295228.1:p.Arg559Gln, XP_047295227.1:p.Arg559Gln, XP_047295248.1:p.Arg509Gln, XP_047295224.1:p.Arg560Gln, XP_047295229.1:p.Arg559Gln, XP_047295249.1:p.Arg509Gln, XP_047295237.1:p.Arg560Gln, XP_047295238.1:p.Arg560Gln, XP_047295247.1:p.Arg558Gln, XP_047295242.1:p.Arg559Gln, XP_047295241.1:p.Arg559Gln, XP_047295246.1:p.Arg558Gln, XP_047295253.1:p.Arg509Gln, XP_047295254.1:p.Arg508Gln, XP_047295225.1:p.Arg560Gln, XP_047295244.1:p.Arg559Gln, XP_047295230.1:p.Arg559Gln, XP_047295218.1:p.Arg589Gln, XP_047295243.1:p.Arg559Gln, XP_047295239.1:p.Arg560Gln, XP_047295245.1:p.Arg559Gln, XP_047295240.1:p.Arg560Gln

                                  17.

                                  rs1477354195 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    19:1621870 (GRCh38)
                                    19:1621869 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:1621869:G:A
                                    Gene:
                                    TCF3 (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000008/2 (TOPMED)
                                    HGVS:
                                    NC_000019.10:g.1621870G>A, NC_000019.9:g.1621869G>A, NG_029953.2:g.35677C>T, NM_003200.5:c.923C>T, NM_003200.4:c.923C>T, NM_003200.3:c.923C>T, NM_001136139.4:c.923C>T, NM_001136139.3:c.923C>T, NM_001136139.2:c.923C>T, NM_001351779.2:c.923C>T, NM_001351779.1:c.923C>T, NM_001351778.2:c.923C>T, NM_001351778.1:c.923C>T, XM_006722855.5:c.1010C>T, XM_006722855.4:c.1010C>T, XM_006722855.3:c.1010C>T, XM_006722855.2:c.1010C>T, XM_006722855.1:c.1010C>T, XM_011528226.3:c.923C>T, XM_011528226.2:c.923C>T, XM_011528226.1:c.923C>T, XM_011528225.3:c.923C>T, XM_011528225.2:c.923C>T, XM_011528225.1:c.923C>T, XM_017027181.2:c.923C>T, XM_017027181.1:c.923C>T, XM_017027178.2:c.1010C>T, XM_017027178.1:c.1010C>T, XM_047439270.1:c.923C>T, XM_047439275.1:c.923C>T, XM_047439263.1:c.923C>T, XM_047439266.1:c.923C>T, XM_047439272.1:c.923C>T, XM_047439271.1:c.923C>T, XM_047439292.1:c.770C>T, XM_047439264.1:c.923C>T, XM_047439267.1:c.923C>T, XM_047439268.1:c.923C>T, XM_047439273.1:c.923C>T, XM_047439293.1:c.770C>T, XM_047439276.1:c.923C>T, XM_047439281.1:c.923C>T, XM_047439258.1:c.1010C>T, XM_047439261.1:c.1010C>T, XM_047439279.1:c.923C>T, XM_047439282.1:c.923C>T, XM_047439291.1:c.923C>T, XM_047439286.1:c.923C>T, XM_047439285.1:c.923C>T, XM_047439290.1:c.923C>T, XM_047439295.1:c.770C>T, XM_047439294.1:c.770C>T, XM_047439297.1:c.770C>T, XM_047439298.1:c.770C>T, XM_047439265.1:c.923C>T, XM_047439269.1:c.923C>T, XM_047439288.1:c.923C>T, XM_047439274.1:c.923C>T, XM_047439260.1:c.1010C>T, XM_047439262.1:c.1010C>T, XM_047439280.1:c.923C>T, XM_047439277.1:c.923C>T, XM_047439287.1:c.923C>T, XM_047439283.1:c.923C>T, XM_047439296.1:c.770C>T, XM_047439259.1:c.1010C>T, XM_047439278.1:c.923C>T, XM_047439289.1:c.923C>T, XM_047439284.1:c.923C>T, NP_003191.1:p.Thr308Met, NP_001129611.1:p.Thr308Met, NP_001338708.1:p.Thr308Met, NP_001338707.1:p.Thr308Met, XP_006722918.1:p.Thr337Met, XP_011526528.1:p.Thr308Met, XP_011526527.1:p.Thr308Met, XP_016882670.1:p.Thr308Met, XP_016882667.1:p.Thr337Met, XP_047295226.1:p.Thr308Met, XP_047295231.1:p.Thr308Met, XP_047295219.1:p.Thr308Met, XP_047295222.1:p.Thr308Met, XP_047295228.1:p.Thr308Met, XP_047295227.1:p.Thr308Met, XP_047295248.1:p.Thr257Met, XP_047295220.1:p.Thr308Met, XP_047295223.1:p.Thr308Met, XP_047295224.1:p.Thr308Met, XP_047295229.1:p.Thr308Met, XP_047295249.1:p.Thr257Met, XP_047295232.1:p.Thr308Met, XP_047295237.1:p.Thr308Met, XP_047295214.1:p.Thr337Met, XP_047295217.1:p.Thr337Met, XP_047295235.1:p.Thr308Met, XP_047295238.1:p.Thr308Met, XP_047295247.1:p.Thr308Met, XP_047295242.1:p.Thr308Met, XP_047295241.1:p.Thr308Met, XP_047295246.1:p.Thr308Met, XP_047295251.1:p.Thr257Met, XP_047295250.1:p.Thr257Met, XP_047295253.1:p.Thr257Met, XP_047295254.1:p.Thr257Met, XP_047295221.1:p.Thr308Met, XP_047295225.1:p.Thr308Met, XP_047295244.1:p.Thr308Met, XP_047295230.1:p.Thr308Met, XP_047295216.1:p.Thr337Met, XP_047295218.1:p.Thr337Met, XP_047295236.1:p.Thr308Met, XP_047295233.1:p.Thr308Met, XP_047295243.1:p.Thr308Met, XP_047295239.1:p.Thr308Met, XP_047295252.1:p.Thr257Met, XP_047295215.1:p.Thr337Met, XP_047295234.1:p.Thr308Met, XP_047295245.1:p.Thr308Met, XP_047295240.1:p.Thr308Met

                                    18.

                                    rs1475251643 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      19:1622134 (GRCh38)
                                      19:1622133 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:1622133:G:A
                                      Gene:
                                      TCF3 (Varview)
                                      Functional Consequence:
                                      missense_variant,coding_sequence_variant
                                      HGVS:
                                      NC_000019.10:g.1622134G>A, NC_000019.9:g.1622133G>A, NG_029953.2:g.35413C>T, NM_003200.5:c.742C>T, NM_003200.4:c.742C>T, NM_003200.3:c.742C>T, NM_001136139.4:c.742C>T, NM_001136139.3:c.742C>T, NM_001136139.2:c.742C>T, NM_001351779.2:c.742C>T, NM_001351779.1:c.742C>T, NM_001351778.2:c.742C>T, NM_001351778.1:c.742C>T, XM_006722855.5:c.829C>T, XM_006722855.4:c.829C>T, XM_006722855.3:c.829C>T, XM_006722855.2:c.829C>T, XM_006722855.1:c.829C>T, XM_011528226.3:c.742C>T, XM_011528226.2:c.742C>T, XM_011528226.1:c.742C>T, XM_011528225.3:c.742C>T, XM_011528225.2:c.742C>T, XM_011528225.1:c.742C>T, XM_017027181.2:c.742C>T, XM_017027181.1:c.742C>T, XM_017027178.2:c.829C>T, XM_017027178.1:c.829C>T, XM_047439270.1:c.742C>T, XM_047439275.1:c.742C>T, XM_047439263.1:c.742C>T, XM_047439266.1:c.742C>T, XM_047439272.1:c.742C>T, XM_047439271.1:c.742C>T, XM_047439292.1:c.589C>T, XM_047439264.1:c.742C>T, XM_047439267.1:c.742C>T, XM_047439268.1:c.742C>T, XM_047439273.1:c.742C>T, XM_047439293.1:c.589C>T, XM_047439276.1:c.742C>T, XM_047439281.1:c.742C>T, XM_047439258.1:c.829C>T, XM_047439261.1:c.829C>T, XM_047439279.1:c.742C>T, XM_047439282.1:c.742C>T, XM_047439291.1:c.742C>T, XM_047439286.1:c.742C>T, XM_047439285.1:c.742C>T, XM_047439290.1:c.742C>T, XM_047439295.1:c.589C>T, XM_047439294.1:c.589C>T, XM_047439297.1:c.589C>T, XM_047439298.1:c.589C>T, XM_047439265.1:c.742C>T, XM_047439269.1:c.742C>T, XM_047439288.1:c.742C>T, XM_047439274.1:c.742C>T, XM_047439260.1:c.829C>T, XM_047439262.1:c.829C>T, XM_047439280.1:c.742C>T, XM_047439277.1:c.742C>T, XM_047439287.1:c.742C>T, XM_047439283.1:c.742C>T, XM_047439296.1:c.589C>T, XM_047439259.1:c.829C>T, XM_047439278.1:c.742C>T, XM_047439289.1:c.742C>T, XM_047439284.1:c.742C>T, NP_003191.1:p.Pro248Ser, NP_001129611.1:p.Pro248Ser, NP_001338708.1:p.Pro248Ser, NP_001338707.1:p.Pro248Ser, XP_006722918.1:p.Pro277Ser, XP_011526528.1:p.Pro248Ser, XP_011526527.1:p.Pro248Ser, XP_016882670.1:p.Pro248Ser, XP_016882667.1:p.Pro277Ser, XP_047295226.1:p.Pro248Ser, XP_047295231.1:p.Pro248Ser, XP_047295219.1:p.Pro248Ser, XP_047295222.1:p.Pro248Ser, XP_047295228.1:p.Pro248Ser, XP_047295227.1:p.Pro248Ser, XP_047295248.1:p.Pro197Ser, XP_047295220.1:p.Pro248Ser, XP_047295223.1:p.Pro248Ser, XP_047295224.1:p.Pro248Ser, XP_047295229.1:p.Pro248Ser, XP_047295249.1:p.Pro197Ser, XP_047295232.1:p.Pro248Ser, XP_047295237.1:p.Pro248Ser, XP_047295214.1:p.Pro277Ser, XP_047295217.1:p.Pro277Ser, XP_047295235.1:p.Pro248Ser, XP_047295238.1:p.Pro248Ser, XP_047295247.1:p.Pro248Ser, XP_047295242.1:p.Pro248Ser, XP_047295241.1:p.Pro248Ser, XP_047295246.1:p.Pro248Ser, XP_047295251.1:p.Pro197Ser, XP_047295250.1:p.Pro197Ser, XP_047295253.1:p.Pro197Ser, XP_047295254.1:p.Pro197Ser, XP_047295221.1:p.Pro248Ser, XP_047295225.1:p.Pro248Ser, XP_047295244.1:p.Pro248Ser, XP_047295230.1:p.Pro248Ser, XP_047295216.1:p.Pro277Ser, XP_047295218.1:p.Pro277Ser, XP_047295236.1:p.Pro248Ser, XP_047295233.1:p.Pro248Ser, XP_047295243.1:p.Pro248Ser, XP_047295239.1:p.Pro248Ser, XP_047295252.1:p.Pro197Ser, XP_047295215.1:p.Pro277Ser, XP_047295234.1:p.Pro248Ser, XP_047295245.1:p.Pro248Ser, XP_047295240.1:p.Pro248Ser

                                      19.

                                      rs1474791414 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A [Show Flanks]
                                        Chromosome:
                                        19:1622098 (GRCh38)
                                        19:1622097 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:1622097:C:A
                                        Gene:
                                        TCF3 (Varview)
                                        Functional Consequence:
                                        stop_gained,coding_sequence_variant
                                        HGVS:
                                        NC_000019.10:g.1622098C>A, NC_000019.9:g.1622097C>A, NG_029953.2:g.35449G>T, NM_003200.5:c.778G>T, NM_003200.4:c.778G>T, NM_003200.3:c.778G>T, NM_001136139.4:c.778G>T, NM_001136139.3:c.778G>T, NM_001136139.2:c.778G>T, NM_001351779.2:c.778G>T, NM_001351779.1:c.778G>T, NM_001351778.2:c.778G>T, NM_001351778.1:c.778G>T, XM_006722855.5:c.865G>T, XM_006722855.4:c.865G>T, XM_006722855.3:c.865G>T, XM_006722855.2:c.865G>T, XM_006722855.1:c.865G>T, XM_011528226.3:c.778G>T, XM_011528226.2:c.778G>T, XM_011528226.1:c.778G>T, XM_011528225.3:c.778G>T, XM_011528225.2:c.778G>T, XM_011528225.1:c.778G>T, XM_017027181.2:c.778G>T, XM_017027181.1:c.778G>T, XM_017027178.2:c.865G>T, XM_017027178.1:c.865G>T, XM_047439270.1:c.778G>T, XM_047439275.1:c.778G>T, XM_047439263.1:c.778G>T, XM_047439266.1:c.778G>T, XM_047439272.1:c.778G>T, XM_047439271.1:c.778G>T, XM_047439292.1:c.625G>T, XM_047439264.1:c.778G>T, XM_047439267.1:c.778G>T, XM_047439268.1:c.778G>T, XM_047439273.1:c.778G>T, XM_047439293.1:c.625G>T, XM_047439276.1:c.778G>T, XM_047439281.1:c.778G>T, XM_047439258.1:c.865G>T, XM_047439261.1:c.865G>T, XM_047439279.1:c.778G>T, XM_047439282.1:c.778G>T, XM_047439291.1:c.778G>T, XM_047439286.1:c.778G>T, XM_047439285.1:c.778G>T, XM_047439290.1:c.778G>T, XM_047439295.1:c.625G>T, XM_047439294.1:c.625G>T, XM_047439297.1:c.625G>T, XM_047439298.1:c.625G>T, XM_047439265.1:c.778G>T, XM_047439269.1:c.778G>T, XM_047439288.1:c.778G>T, XM_047439274.1:c.778G>T, XM_047439260.1:c.865G>T, XM_047439262.1:c.865G>T, XM_047439280.1:c.778G>T, XM_047439277.1:c.778G>T, XM_047439287.1:c.778G>T, XM_047439283.1:c.778G>T, XM_047439296.1:c.625G>T, XM_047439259.1:c.865G>T, XM_047439278.1:c.778G>T, XM_047439289.1:c.778G>T, XM_047439284.1:c.778G>T, NP_003191.1:p.Gly260Ter, NP_001129611.1:p.Gly260Ter, NP_001338708.1:p.Gly260Ter, NP_001338707.1:p.Gly260Ter, XP_006722918.1:p.Gly289Ter, XP_011526528.1:p.Gly260Ter, XP_011526527.1:p.Gly260Ter, XP_016882670.1:p.Gly260Ter, XP_016882667.1:p.Gly289Ter, XP_047295226.1:p.Gly260Ter, XP_047295231.1:p.Gly260Ter, XP_047295219.1:p.Gly260Ter, XP_047295222.1:p.Gly260Ter, XP_047295228.1:p.Gly260Ter, XP_047295227.1:p.Gly260Ter, XP_047295248.1:p.Gly209Ter, XP_047295220.1:p.Gly260Ter, XP_047295223.1:p.Gly260Ter, XP_047295224.1:p.Gly260Ter, XP_047295229.1:p.Gly260Ter, XP_047295249.1:p.Gly209Ter, XP_047295232.1:p.Gly260Ter, XP_047295237.1:p.Gly260Ter, XP_047295214.1:p.Gly289Ter, XP_047295217.1:p.Gly289Ter, XP_047295235.1:p.Gly260Ter, XP_047295238.1:p.Gly260Ter, XP_047295247.1:p.Gly260Ter, XP_047295242.1:p.Gly260Ter, XP_047295241.1:p.Gly260Ter, XP_047295246.1:p.Gly260Ter, XP_047295251.1:p.Gly209Ter, XP_047295250.1:p.Gly209Ter, XP_047295253.1:p.Gly209Ter, XP_047295254.1:p.Gly209Ter, XP_047295221.1:p.Gly260Ter, XP_047295225.1:p.Gly260Ter, XP_047295244.1:p.Gly260Ter, XP_047295230.1:p.Gly260Ter, XP_047295216.1:p.Gly289Ter, XP_047295218.1:p.Gly289Ter, XP_047295236.1:p.Gly260Ter, XP_047295233.1:p.Gly260Ter, XP_047295243.1:p.Gly260Ter, XP_047295239.1:p.Gly260Ter, XP_047295252.1:p.Gly209Ter, XP_047295215.1:p.Gly289Ter, XP_047295234.1:p.Gly260Ter, XP_047295245.1:p.Gly260Ter, XP_047295240.1:p.Gly260Ter

                                        20.

                                        rs1472833671 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          19:1621176 (GRCh38)
                                          19:1621175 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:1621175:G:A
                                          Gene:
                                          TCF3 (Varview)
                                          Functional Consequence:
                                          missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000021/3 (GnomAD_exomes)
                                          A=0.000546/1 (Korea1K)
                                          A=0.002055/6 (KOREAN)
                                          A=0.003645/61 (TOMMO)
                                          HGVS:
                                          NC_000019.10:g.1621176G>A, NC_000019.9:g.1621175G>A, NG_029953.2:g.36371C>T, NM_003200.5:c.971C>T, NM_003200.4:c.971C>T, NM_003200.3:c.971C>T, NM_001136139.4:c.971C>T, NM_001136139.3:c.971C>T, NM_001136139.2:c.971C>T, NM_001351779.2:c.971C>T, NM_001351779.1:c.971C>T, NM_001351778.2:c.971C>T, NM_001351778.1:c.971C>T, XM_006722855.5:c.1058C>T, XM_006722855.4:c.1058C>T, XM_006722855.3:c.1058C>T, XM_006722855.2:c.1058C>T, XM_006722855.1:c.1058C>T, XM_011528226.3:c.971C>T, XM_011528226.2:c.971C>T, XM_011528226.1:c.971C>T, XM_011528225.3:c.971C>T, XM_011528225.2:c.971C>T, XM_011528225.1:c.971C>T, XM_017027181.2:c.971C>T, XM_017027181.1:c.971C>T, XM_017027178.2:c.1058C>T, XM_017027178.1:c.1058C>T, XM_047439270.1:c.971C>T, XM_047439275.1:c.971C>T, XM_047439263.1:c.971C>T, XM_047439266.1:c.971C>T, XM_047439272.1:c.971C>T, XM_047439271.1:c.971C>T, XM_047439292.1:c.818C>T, XM_047439264.1:c.971C>T, XM_047439267.1:c.971C>T, XM_047439268.1:c.971C>T, XM_047439273.1:c.971C>T, XM_047439293.1:c.818C>T, XM_047439276.1:c.971C>T, XM_047439281.1:c.971C>T, XM_047439258.1:c.1058C>T, XM_047439261.1:c.1058C>T, XM_047439279.1:c.971C>T, XM_047439282.1:c.971C>T, XM_047439291.1:c.971C>T, XM_047439286.1:c.971C>T, XM_047439285.1:c.971C>T, XM_047439290.1:c.971C>T, XM_047439295.1:c.818C>T, XM_047439294.1:c.818C>T, XM_047439297.1:c.818C>T, XM_047439298.1:c.818C>T, XM_047439265.1:c.971C>T, XM_047439269.1:c.971C>T, XM_047439288.1:c.971C>T, XM_047439274.1:c.971C>T, XM_047439260.1:c.1058C>T, XM_047439262.1:c.1058C>T, XM_047439280.1:c.971C>T, XM_047439277.1:c.971C>T, XM_047439287.1:c.971C>T, XM_047439283.1:c.971C>T, XM_047439296.1:c.818C>T, XM_047439259.1:c.1058C>T, XM_047439278.1:c.971C>T, XM_047439289.1:c.971C>T, XM_047439284.1:c.971C>T, NP_003191.1:p.Thr324Ile, NP_001129611.1:p.Thr324Ile, NP_001338708.1:p.Thr324Ile, NP_001338707.1:p.Thr324Ile, XP_006722918.1:p.Thr353Ile, XP_011526528.1:p.Thr324Ile, XP_011526527.1:p.Thr324Ile, XP_016882670.1:p.Thr324Ile, XP_016882667.1:p.Thr353Ile, XP_047295226.1:p.Thr324Ile, XP_047295231.1:p.Thr324Ile, XP_047295219.1:p.Thr324Ile, XP_047295222.1:p.Thr324Ile, XP_047295228.1:p.Thr324Ile, XP_047295227.1:p.Thr324Ile, XP_047295248.1:p.Thr273Ile, XP_047295220.1:p.Thr324Ile, XP_047295223.1:p.Thr324Ile, XP_047295224.1:p.Thr324Ile, XP_047295229.1:p.Thr324Ile, XP_047295249.1:p.Thr273Ile, XP_047295232.1:p.Thr324Ile, XP_047295237.1:p.Thr324Ile, XP_047295214.1:p.Thr353Ile, XP_047295217.1:p.Thr353Ile, XP_047295235.1:p.Thr324Ile, XP_047295238.1:p.Thr324Ile, XP_047295247.1:p.Thr324Ile, XP_047295242.1:p.Thr324Ile, XP_047295241.1:p.Thr324Ile, XP_047295246.1:p.Thr324Ile, XP_047295251.1:p.Thr273Ile, XP_047295250.1:p.Thr273Ile, XP_047295253.1:p.Thr273Ile, XP_047295254.1:p.Thr273Ile, XP_047295221.1:p.Thr324Ile, XP_047295225.1:p.Thr324Ile, XP_047295244.1:p.Thr324Ile, XP_047295230.1:p.Thr324Ile, XP_047295216.1:p.Thr353Ile, XP_047295218.1:p.Thr353Ile, XP_047295236.1:p.Thr324Ile, XP_047295233.1:p.Thr324Ile, XP_047295243.1:p.Thr324Ile, XP_047295239.1:p.Thr324Ile, XP_047295252.1:p.Thr273Ile, XP_047295215.1:p.Thr353Ile, XP_047295234.1:p.Thr324Ile, XP_047295245.1:p.Thr324Ile, XP_047295240.1:p.Thr324Ile

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