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Items: 1 to 20 of 413

1.

rs1490764084 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    14:102905779 (GRCh38)
    14:103372116 (GRCh37)
    Canonical SPDI:
    NC_000014.9:102905778:C:T
    Gene:
    TRAF3 (Varview)
    Functional Consequence:
    coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
    HGVS:
    NC_000014.9:g.102905779C>T, NC_000014.8:g.103372116C>T, NG_027973.1:g.133301C>T, NM_003300.4:c.1702C>T, NM_003300.3:c.1702C>T, NM_145725.3:c.1702C>T, NM_145725.2:c.1702C>T, NM_145726.3:c.1627C>T, NM_145726.2:c.1627C>T, NM_001199427.2:c.1453C>T, NM_001199427.1:c.1453C>T, NM_001385143.1:c.1621C>T, NM_001385142.1:c.1561C>T, XM_011537116.4:c.1546C>T, XM_011537116.3:c.1546C>T, XM_011537116.2:c.1546C>T, XM_011537116.1:c.1546C>T, XM_011537117.4:c.1534C>T, XM_011537117.3:c.1534C>T, XM_011537117.2:c.1534C>T, XM_011537117.1:c.1534C>T, XM_011537118.4:c.1453C>T, XM_011537118.3:c.1453C>T, XM_011537118.2:c.1453C>T, XM_011537118.1:c.1453C>T, XM_017021618.2:c.1702C>T, XM_017021618.1:c.1702C>T, XM_017021619.2:c.1627C>T, XM_017021619.1:c.1627C>T, XM_017021617.2:c.1702C>T, XM_017021617.1:c.1702C>T, XM_047431741.1:c.1534C>T, XM_047431738.1:c.1702C>T, XM_047431739.1:c.1627C>T, XM_047431740.1:c.1546C>T, XM_047431742.1:c.1534C>T, NP_003291.2:p.Pro568Ser, NP_663777.1:p.Pro568Ser, NP_663778.1:p.Pro543Ser, NP_001186356.1:p.Pro485Ser, NP_001372072.1:p.Pro541Ser, NP_001372071.1:p.Pro521Ser, XP_011535418.1:p.Pro516Ser, XP_011535419.1:p.Pro512Ser, XP_011535420.1:p.Pro485Ser, XP_016877107.1:p.Pro568Ser, XP_016877108.1:p.Pro543Ser, XP_016877106.1:p.Pro568Ser, XP_047287697.1:p.Pro512Ser, XP_047287694.1:p.Pro568Ser, XP_047287695.1:p.Pro543Ser, XP_047287696.1:p.Pro516Ser, XP_047287698.1:p.Pro512Ser

    2.

    rs1488603356 [Homo sapiens]
      Variant type:
      INS
      Alleles:
      ->ATCCGTAGTTCC [Show Flanks]
      Chromosome:
      14:102897316 (GRCh38)
      14:103363654 (GRCh37)
      Canonical SPDI:
      NC_000014.9:102897316::ATCCGTAGTTCC
      Gene:
      TRAF3 (Varview)
      Functional Consequence:
      coding_sequence_variant,intron_variant,inframe_indel,genic_downstream_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      ATCCGTAGTTCC=0.0001/1 (ALFA)
      HGVS:
      NC_000014.9:g.102897316_102897317insATCCGTAGTTCC, NC_000014.8:g.103363653_103363654insATCCGTAGTTCC, NG_027973.1:g.124838_124839insATCCGTAGTTCC, NM_003300.4:c.875_876insATCCGTAGTTCC, NM_003300.3:c.875_876insATCCGTAGTTCC, NM_145725.3:c.875_876insATCCGTAGTTCC, NM_145725.2:c.875_876insATCCGTAGTTCC, NM_145726.3:c.800_801insATCCGTAGTTCC, NM_145726.2:c.800_801insATCCGTAGTTCC, NM_001199427.2:c.626_627insATCCGTAGTTCC, NM_001199427.1:c.626_627insATCCGTAGTTCC, NM_001385143.1:c.794_795insATCCGTAGTTCC, XM_011537116.4:c.719_720insATCCGTAGTTCC, XM_011537116.3:c.719_720insATCCGTAGTTCC, XM_011537116.2:c.719_720insATCCGTAGTTCC, XM_011537116.1:c.719_720insATCCGTAGTTCC, XM_011537117.4:c.707_708insATCCGTAGTTCC, XM_011537117.3:c.707_708insATCCGTAGTTCC, XM_011537117.2:c.707_708insATCCGTAGTTCC, XM_011537117.1:c.707_708insATCCGTAGTTCC, XM_011537118.4:c.626_627insATCCGTAGTTCC, XM_011537118.3:c.626_627insATCCGTAGTTCC, XM_011537118.2:c.626_627insATCCGTAGTTCC, XM_011537118.1:c.626_627insATCCGTAGTTCC, XM_017021618.2:c.875_876insATCCGTAGTTCC, XM_017021618.1:c.875_876insATCCGTAGTTCC, XM_017021619.2:c.800_801insATCCGTAGTTCC, XM_017021619.1:c.800_801insATCCGTAGTTCC, XM_017021617.2:c.875_876insATCCGTAGTTCC, XM_017021617.1:c.875_876insATCCGTAGTTCC, XM_047431741.1:c.707_708insATCCGTAGTTCC, XM_047431738.1:c.875_876insATCCGTAGTTCC, XM_047431739.1:c.800_801insATCCGTAGTTCC, XM_047431740.1:c.719_720insATCCGTAGTTCC, XM_047431742.1:c.707_708insATCCGTAGTTCC, NP_003291.2:p.His292delinsGlnSerValValPro, NP_663777.1:p.His292delinsGlnSerValValPro, NP_663778.1:p.His267delinsGlnSerValValPro, NP_001186356.1:p.His209delinsGlnSerValValPro, NP_001372072.1:p.His265delinsGlnSerValValPro, XP_011535418.1:p.His240delinsGlnSerValValPro, XP_011535419.1:p.His236delinsGlnSerValValPro, XP_011535420.1:p.His209delinsGlnSerValValPro, XP_016877107.1:p.His292delinsGlnSerValValPro, XP_016877108.1:p.His267delinsGlnSerValValPro, XP_016877106.1:p.His292delinsGlnSerValValPro, XP_047287697.1:p.His236delinsGlnSerValValPro, XP_047287694.1:p.His292delinsGlnSerValValPro, XP_047287695.1:p.His267delinsGlnSerValValPro, XP_047287696.1:p.His240delinsGlnSerValValPro, XP_047287698.1:p.His236delinsGlnSerValValPro

      3.

      rs1483147036 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        14:102876360 (GRCh38)
        14:103342697 (GRCh37)
        Canonical SPDI:
        NC_000014.9:102876359:G:A
        Gene:
        TRAF3 (Varview)
        Functional Consequence:
        coding_sequence_variant,synonymous_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0./0 (ALFA)
        A=0.000004/1 (TOPMED)
        A=0.000029/4 (GnomAD)
        HGVS:
        NC_000014.9:g.102876360G>A, NC_000014.8:g.103342697G>A, NG_027973.1:g.103882G>A, NM_003300.4:c.405G>A, NM_003300.3:c.405G>A, NM_145725.3:c.405G>A, NM_145725.2:c.405G>A, NM_145726.3:c.405G>A, NM_145726.2:c.405G>A, NM_001199427.2:c.405G>A, NM_001199427.1:c.405G>A, NM_001385143.1:c.405G>A, NM_001385142.1:c.405G>A, XM_011537116.4:c.405G>A, XM_011537116.3:c.405G>A, XM_011537116.2:c.405G>A, XM_011537116.1:c.405G>A, XM_011537117.4:c.405G>A, XM_011537117.3:c.405G>A, XM_011537117.2:c.405G>A, XM_011537117.1:c.405G>A, XM_011537118.4:c.405G>A, XM_011537118.3:c.405G>A, XM_011537118.2:c.405G>A, XM_011537118.1:c.405G>A, XM_017021620.3:c.405G>A, XM_017021620.2:c.405G>A, XM_017021620.1:c.405G>A, XM_017021618.2:c.405G>A, XM_017021618.1:c.405G>A, XM_017021619.2:c.405G>A, XM_017021619.1:c.405G>A, XM_017021617.2:c.405G>A, XM_017021617.1:c.405G>A, XM_047431741.1:c.405G>A, XM_047431738.1:c.405G>A, XM_047431739.1:c.405G>A, XM_047431740.1:c.405G>A, XM_047431742.1:c.405G>A

        4.

        rs1481129494 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G [Show Flanks]
          Chromosome:
          14:102876444 (GRCh38)
          14:103342781 (GRCh37)
          Canonical SPDI:
          NC_000014.9:102876443:A:G
          Gene:
          TRAF3 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0.000071/1 (ALFA)
          G=0.000024/6 (GnomAD_exomes)
          G=0.00003/8 (TOPMED)
          G=0.000043/6 (GnomAD)
          HGVS:
          NC_000014.9:g.102876444A>G, NC_000014.8:g.103342781A>G, NG_027973.1:g.103966A>G, NM_003300.4:c.489A>G, NM_003300.3:c.489A>G, NM_145725.3:c.489A>G, NM_145725.2:c.489A>G, NM_145726.3:c.489A>G, NM_145726.2:c.489A>G, NM_001199427.2:c.489A>G, NM_001199427.1:c.489A>G, NM_001385143.1:c.489A>G, NM_001385142.1:c.489A>G, XM_011537116.4:c.489A>G, XM_011537116.3:c.489A>G, XM_011537116.2:c.489A>G, XM_011537116.1:c.489A>G, XM_011537117.4:c.489A>G, XM_011537117.3:c.489A>G, XM_011537117.2:c.489A>G, XM_011537117.1:c.489A>G, XM_011537118.4:c.489A>G, XM_011537118.3:c.489A>G, XM_011537118.2:c.489A>G, XM_011537118.1:c.489A>G, XM_017021620.3:c.489A>G, XM_017021620.2:c.489A>G, XM_017021620.1:c.489A>G, XM_017021618.2:c.489A>G, XM_017021618.1:c.489A>G, XM_017021619.2:c.489A>G, XM_017021619.1:c.489A>G, XM_017021617.2:c.489A>G, XM_017021617.1:c.489A>G, XM_047431741.1:c.489A>G, XM_047431738.1:c.489A>G, XM_047431739.1:c.489A>G, XM_047431740.1:c.489A>G, XM_047431742.1:c.489A>G

          5.

          rs1481082601 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A,T [Show Flanks]
            Chromosome:
            14:102903294 (GRCh38)
            14:103369631 (GRCh37)
            Canonical SPDI:
            NC_000014.9:102903293:G:A,NC_000014.9:102903293:G:T
            Gene:
            TRAF3 (Varview)
            Functional Consequence:
            coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            A=0.000007/1 (GnomAD)
            HGVS:
            NC_000014.9:g.102903294G>A, NC_000014.9:g.102903294G>T, NC_000014.8:g.103369631G>A, NC_000014.8:g.103369631G>T, NG_027973.1:g.130816G>A, NG_027973.1:g.130816G>T, NM_003300.4:c.1000G>A, NM_003300.4:c.1000G>T, NM_003300.3:c.1000G>A, NM_003300.3:c.1000G>T, NM_145725.3:c.1000G>A, NM_145725.3:c.1000G>T, NM_145725.2:c.1000G>A, NM_145725.2:c.1000G>T, NM_145726.3:c.925G>A, NM_145726.3:c.925G>T, NM_145726.2:c.925G>A, NM_145726.2:c.925G>T, NM_001199427.2:c.751G>A, NM_001199427.2:c.751G>T, NM_001199427.1:c.751G>A, NM_001199427.1:c.751G>T, NM_001385143.1:c.919G>A, NM_001385143.1:c.919G>T, NM_001385142.1:c.859G>A, NM_001385142.1:c.859G>T, XM_011537116.4:c.844G>A, XM_011537116.4:c.844G>T, XM_011537116.3:c.844G>A, XM_011537116.3:c.844G>T, XM_011537116.2:c.844G>A, XM_011537116.2:c.844G>T, XM_011537116.1:c.844G>A, XM_011537116.1:c.844G>T, XM_011537117.4:c.832G>A, XM_011537117.4:c.832G>T, XM_011537117.3:c.832G>A, XM_011537117.3:c.832G>T, XM_011537117.2:c.832G>A, XM_011537117.2:c.832G>T, XM_011537117.1:c.832G>A, XM_011537117.1:c.832G>T, XM_011537118.4:c.751G>A, XM_011537118.4:c.751G>T, XM_011537118.3:c.751G>A, XM_011537118.3:c.751G>T, XM_011537118.2:c.751G>A, XM_011537118.2:c.751G>T, XM_011537118.1:c.751G>A, XM_011537118.1:c.751G>T, XM_017021618.2:c.1000G>A, XM_017021618.2:c.1000G>T, XM_017021618.1:c.1000G>A, XM_017021618.1:c.1000G>T, XM_017021619.2:c.925G>A, XM_017021619.2:c.925G>T, XM_017021619.1:c.925G>A, XM_017021619.1:c.925G>T, XM_017021617.2:c.1000G>A, XM_017021617.2:c.1000G>T, XM_017021617.1:c.1000G>A, XM_017021617.1:c.1000G>T, XM_047431741.1:c.832G>A, XM_047431741.1:c.832G>T, XM_047431738.1:c.1000G>A, XM_047431738.1:c.1000G>T, XM_047431739.1:c.925G>A, XM_047431739.1:c.925G>T, XM_047431740.1:c.844G>A, XM_047431740.1:c.844G>T, XM_047431742.1:c.832G>A, XM_047431742.1:c.832G>T, NP_003291.2:p.Asp334Asn, NP_003291.2:p.Asp334Tyr, NP_663777.1:p.Asp334Asn, NP_663777.1:p.Asp334Tyr, NP_663778.1:p.Asp309Asn, NP_663778.1:p.Asp309Tyr, NP_001186356.1:p.Asp251Asn, NP_001186356.1:p.Asp251Tyr, NP_001372072.1:p.Asp307Asn, NP_001372072.1:p.Asp307Tyr, NP_001372071.1:p.Asp287Asn, NP_001372071.1:p.Asp287Tyr, XP_011535418.1:p.Asp282Asn, XP_011535418.1:p.Asp282Tyr, XP_011535419.1:p.Asp278Asn, XP_011535419.1:p.Asp278Tyr, XP_011535420.1:p.Asp251Asn, XP_011535420.1:p.Asp251Tyr, XP_016877107.1:p.Asp334Asn, XP_016877107.1:p.Asp334Tyr, XP_016877108.1:p.Asp309Asn, XP_016877108.1:p.Asp309Tyr, XP_016877106.1:p.Asp334Asn, XP_016877106.1:p.Asp334Tyr, XP_047287697.1:p.Asp278Asn, XP_047287697.1:p.Asp278Tyr, XP_047287694.1:p.Asp334Asn, XP_047287694.1:p.Asp334Tyr, XP_047287695.1:p.Asp309Asn, XP_047287695.1:p.Asp309Tyr, XP_047287696.1:p.Asp282Asn, XP_047287696.1:p.Asp282Tyr, XP_047287698.1:p.Asp278Asn, XP_047287698.1:p.Asp278Tyr

            6.

            rs1471137148 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>T [Show Flanks]
              Chromosome:
              14:102875647 (GRCh38)
              14:103341984 (GRCh37)
              Canonical SPDI:
              NC_000014.9:102875646:G:T
              Gene:
              TRAF3 (Varview)
              Functional Consequence:
              missense_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0./0 (ALFA)
              T=0.000004/1 (TOPMED)
              HGVS:
              NC_000014.9:g.102875647G>T, NC_000014.8:g.103341984G>T, NG_027973.1:g.103169G>T, NM_003300.4:c.321G>T, NM_003300.3:c.321G>T, NM_145725.3:c.321G>T, NM_145725.2:c.321G>T, NM_145726.3:c.321G>T, NM_145726.2:c.321G>T, NM_001199427.2:c.321G>T, NM_001199427.1:c.321G>T, NM_001385143.1:c.321G>T, NM_001385142.1:c.321G>T, XM_011537116.4:c.321G>T, XM_011537116.3:c.321G>T, XM_011537116.2:c.321G>T, XM_011537116.1:c.321G>T, XM_011537117.4:c.321G>T, XM_011537117.3:c.321G>T, XM_011537117.2:c.321G>T, XM_011537117.1:c.321G>T, XM_011537118.4:c.321G>T, XM_011537118.3:c.321G>T, XM_011537118.2:c.321G>T, XM_011537118.1:c.321G>T, XM_017021620.3:c.321G>T, XM_017021620.2:c.321G>T, XM_017021620.1:c.321G>T, XM_017021618.2:c.321G>T, XM_017021618.1:c.321G>T, XM_017021619.2:c.321G>T, XM_017021619.1:c.321G>T, XM_017021617.2:c.321G>T, XM_017021617.1:c.321G>T, XM_047431741.1:c.321G>T, XM_047431738.1:c.321G>T, XM_047431739.1:c.321G>T, XM_047431740.1:c.321G>T, XM_047431742.1:c.321G>T, NP_003291.2:p.Lys107Asn, NP_663777.1:p.Lys107Asn, NP_663778.1:p.Lys107Asn, NP_001186356.1:p.Lys107Asn, NP_001372072.1:p.Lys107Asn, NP_001372071.1:p.Lys107Asn, XP_011535418.1:p.Lys107Asn, XP_011535419.1:p.Lys107Asn, XP_011535420.1:p.Lys107Asn, XP_016877109.1:p.Lys107Asn, XP_016877107.1:p.Lys107Asn, XP_016877108.1:p.Lys107Asn, XP_016877106.1:p.Lys107Asn, XP_047287697.1:p.Lys107Asn, XP_047287694.1:p.Lys107Asn, XP_047287695.1:p.Lys107Asn, XP_047287696.1:p.Lys107Asn, XP_047287698.1:p.Lys107Asn

              7.

              rs1471110963 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>G [Show Flanks]
                Chromosome:
                14:102905556 (GRCh38)
                14:103371893 (GRCh37)
                Canonical SPDI:
                NC_000014.9:102905555:A:G
                Gene:
                TRAF3 (Varview)
                Functional Consequence:
                synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
                Validated:
                by frequency
                MAF:
                G=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000014.9:g.102905556A>G, NC_000014.8:g.103371893A>G, NG_027973.1:g.133078A>G, NM_003300.4:c.1479A>G, NM_003300.3:c.1479A>G, NM_145725.3:c.1479A>G, NM_145725.2:c.1479A>G, NM_145726.3:c.1404A>G, NM_145726.2:c.1404A>G, NM_001199427.2:c.1230A>G, NM_001199427.1:c.1230A>G, NM_001385143.1:c.1398A>G, NM_001385142.1:c.1338A>G, XM_011537116.4:c.1323A>G, XM_011537116.3:c.1323A>G, XM_011537116.2:c.1323A>G, XM_011537116.1:c.1323A>G, XM_011537117.4:c.1311A>G, XM_011537117.3:c.1311A>G, XM_011537117.2:c.1311A>G, XM_011537117.1:c.1311A>G, XM_011537118.4:c.1230A>G, XM_011537118.3:c.1230A>G, XM_011537118.2:c.1230A>G, XM_011537118.1:c.1230A>G, XM_017021618.2:c.1479A>G, XM_017021618.1:c.1479A>G, XM_017021619.2:c.1404A>G, XM_017021619.1:c.1404A>G, XM_017021617.2:c.1479A>G, XM_017021617.1:c.1479A>G, XM_047431741.1:c.1311A>G, XM_047431738.1:c.1479A>G, XM_047431739.1:c.1404A>G, XM_047431740.1:c.1323A>G, XM_047431742.1:c.1311A>G

                8.

                rs1469059204 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  14:102870270 (GRCh38)
                  14:103336607 (GRCh37)
                  Canonical SPDI:
                  NC_000014.9:102870269:T:C
                  Gene:
                  TRAF3 (Varview)
                  Functional Consequence:
                  synonymous_variant,coding_sequence_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000014.9:g.102870270T>C, NC_000014.8:g.103336607T>C, NG_027973.1:g.97792T>C, NM_003300.4:c.69T>C, NM_003300.3:c.69T>C, NM_145725.3:c.69T>C, NM_145725.2:c.69T>C, NM_145726.3:c.69T>C, NM_145726.2:c.69T>C, NM_001199427.2:c.69T>C, NM_001199427.1:c.69T>C, NM_001385143.1:c.69T>C, NM_001385142.1:c.69T>C, XM_011537116.4:c.69T>C, XM_011537116.3:c.69T>C, XM_011537116.2:c.69T>C, XM_011537116.1:c.69T>C, XM_011537117.4:c.69T>C, XM_011537117.3:c.69T>C, XM_011537117.2:c.69T>C, XM_011537117.1:c.69T>C, XM_011537118.4:c.69T>C, XM_011537118.3:c.69T>C, XM_011537118.2:c.69T>C, XM_011537118.1:c.69T>C, XM_017021620.3:c.69T>C, XM_017021620.2:c.69T>C, XM_017021620.1:c.69T>C, XM_017021618.2:c.69T>C, XM_017021618.1:c.69T>C, XM_017021619.2:c.69T>C, XM_017021619.1:c.69T>C, XM_017021617.2:c.69T>C, XM_017021617.1:c.69T>C, XM_047431741.1:c.69T>C, XM_047431738.1:c.69T>C, XM_047431739.1:c.69T>C, XM_047431740.1:c.69T>C, XM_047431742.1:c.69T>C

                  9.

                  rs1466838253 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    14:102876520 (GRCh38)
                    14:103342857 (GRCh37)
                    Canonical SPDI:
                    NC_000014.9:102876519:C:T
                    Gene:
                    TRAF3 (Varview)
                    Functional Consequence:
                    synonymous_variant,coding_sequence_variant
                    Validated:
                    by frequency,by cluster
                    MAF:
                    T=0.000004/1 (GnomAD_exomes)
                    T=0.001027/3 (KOREAN)
                    HGVS:
                    NC_000014.9:g.102876520C>T, NC_000014.8:g.103342857C>T, NG_027973.1:g.104042C>T, NM_003300.4:c.565C>T, NM_003300.3:c.565C>T, NM_145725.3:c.565C>T, NM_145725.2:c.565C>T, NM_145726.3:c.565C>T, NM_145726.2:c.565C>T, NM_001199427.2:c.565C>T, NM_001199427.1:c.565C>T, NM_001385143.1:c.565C>T, NM_001385142.1:c.565C>T, XM_011537116.4:c.565C>T, XM_011537116.3:c.565C>T, XM_011537116.2:c.565C>T, XM_011537116.1:c.565C>T, XM_011537117.4:c.565C>T, XM_011537117.3:c.565C>T, XM_011537117.2:c.565C>T, XM_011537117.1:c.565C>T, XM_011537118.4:c.565C>T, XM_011537118.3:c.565C>T, XM_011537118.2:c.565C>T, XM_011537118.1:c.565C>T, XM_017021620.3:c.565C>T, XM_017021620.2:c.565C>T, XM_017021620.1:c.565C>T, XM_017021618.2:c.565C>T, XM_017021618.1:c.565C>T, XM_017021619.2:c.565C>T, XM_017021619.1:c.565C>T, XM_017021617.2:c.565C>T, XM_017021617.1:c.565C>T, XM_047431741.1:c.565C>T, XM_047431738.1:c.565C>T, XM_047431739.1:c.565C>T, XM_047431740.1:c.565C>T, XM_047431742.1:c.565C>T

                    10.

                    rs1464145387 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      14:102903349 (GRCh38)
                      14:103369686 (GRCh37)
                      Canonical SPDI:
                      NC_000014.9:102903348:G:A
                      Gene:
                      TRAF3 (Varview)
                      Functional Consequence:
                      missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000004/1 (TOPMED)
                      HGVS:
                      NC_000014.9:g.102903349G>A, NC_000014.8:g.103369686G>A, NG_027973.1:g.130871G>A, NM_003300.4:c.1055G>A, NM_003300.3:c.1055G>A, NM_145725.3:c.1055G>A, NM_145725.2:c.1055G>A, NM_145726.3:c.980G>A, NM_145726.2:c.980G>A, NM_001199427.2:c.806G>A, NM_001199427.1:c.806G>A, NM_001385143.1:c.974G>A, NM_001385142.1:c.914G>A, XM_011537116.4:c.899G>A, XM_011537116.3:c.899G>A, XM_011537116.2:c.899G>A, XM_011537116.1:c.899G>A, XM_011537117.4:c.887G>A, XM_011537117.3:c.887G>A, XM_011537117.2:c.887G>A, XM_011537117.1:c.887G>A, XM_011537118.4:c.806G>A, XM_011537118.3:c.806G>A, XM_011537118.2:c.806G>A, XM_011537118.1:c.806G>A, XM_017021618.2:c.1055G>A, XM_017021618.1:c.1055G>A, XM_017021619.2:c.980G>A, XM_017021619.1:c.980G>A, XM_017021617.2:c.1055G>A, XM_017021617.1:c.1055G>A, XM_047431741.1:c.887G>A, XM_047431738.1:c.1055G>A, XM_047431739.1:c.980G>A, XM_047431740.1:c.899G>A, XM_047431742.1:c.887G>A, NP_003291.2:p.Ser352Asn, NP_663777.1:p.Ser352Asn, NP_663778.1:p.Ser327Asn, NP_001186356.1:p.Ser269Asn, NP_001372072.1:p.Ser325Asn, NP_001372071.1:p.Ser305Asn, XP_011535418.1:p.Ser300Asn, XP_011535419.1:p.Ser296Asn, XP_011535420.1:p.Ser269Asn, XP_016877107.1:p.Ser352Asn, XP_016877108.1:p.Ser327Asn, XP_016877106.1:p.Ser352Asn, XP_047287697.1:p.Ser296Asn, XP_047287694.1:p.Ser352Asn, XP_047287695.1:p.Ser327Asn, XP_047287696.1:p.Ser300Asn, XP_047287698.1:p.Ser296Asn

                      11.

                      rs1464050160 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>T [Show Flanks]
                        Chromosome:
                        14:102876371 (GRCh38)
                        14:103342708 (GRCh37)
                        Canonical SPDI:
                        NC_000014.9:102876370:A:T
                        Gene:
                        TRAF3 (Varview)
                        Functional Consequence:
                        missense_variant,coding_sequence_variant
                        Validated:
                        by frequency
                        MAF:
                        T=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000014.9:g.102876371A>T, NC_000014.8:g.103342708A>T, NG_027973.1:g.103893A>T, NM_003300.4:c.416A>T, NM_003300.3:c.416A>T, NM_145725.3:c.416A>T, NM_145725.2:c.416A>T, NM_145726.3:c.416A>T, NM_145726.2:c.416A>T, NM_001199427.2:c.416A>T, NM_001199427.1:c.416A>T, NM_001385143.1:c.416A>T, NM_001385142.1:c.416A>T, XM_011537116.4:c.416A>T, XM_011537116.3:c.416A>T, XM_011537116.2:c.416A>T, XM_011537116.1:c.416A>T, XM_011537117.4:c.416A>T, XM_011537117.3:c.416A>T, XM_011537117.2:c.416A>T, XM_011537117.1:c.416A>T, XM_011537118.4:c.416A>T, XM_011537118.3:c.416A>T, XM_011537118.2:c.416A>T, XM_011537118.1:c.416A>T, XM_017021620.3:c.416A>T, XM_017021620.2:c.416A>T, XM_017021620.1:c.416A>T, XM_017021618.2:c.416A>T, XM_017021618.1:c.416A>T, XM_017021619.2:c.416A>T, XM_017021619.1:c.416A>T, XM_017021617.2:c.416A>T, XM_017021617.1:c.416A>T, XM_047431741.1:c.416A>T, XM_047431738.1:c.416A>T, XM_047431739.1:c.416A>T, XM_047431740.1:c.416A>T, XM_047431742.1:c.416A>T, NP_003291.2:p.Asn139Ile, NP_663777.1:p.Asn139Ile, NP_663778.1:p.Asn139Ile, NP_001186356.1:p.Asn139Ile, NP_001372072.1:p.Asn139Ile, NP_001372071.1:p.Asn139Ile, XP_011535418.1:p.Asn139Ile, XP_011535419.1:p.Asn139Ile, XP_011535420.1:p.Asn139Ile, XP_016877109.1:p.Asn139Ile, XP_016877107.1:p.Asn139Ile, XP_016877108.1:p.Asn139Ile, XP_016877106.1:p.Asn139Ile, XP_047287697.1:p.Asn139Ile, XP_047287694.1:p.Asn139Ile, XP_047287695.1:p.Asn139Ile, XP_047287696.1:p.Asn139Ile, XP_047287698.1:p.Asn139Ile

                        12.

                        rs1463441936 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>G [Show Flanks]
                          Chromosome:
                          14:102886233 (GRCh38)
                          14:103352570 (GRCh37)
                          Canonical SPDI:
                          NC_000014.9:102886232:T:G
                          Gene:
                          TRAF3 (Varview)
                          Functional Consequence:
                          synonymous_variant,intron_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000007/1 (GnomAD)
                          HGVS:

                          13.

                          rs1462259878 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            14:102891406 (GRCh38)
                            14:103357743 (GRCh37)
                            Canonical SPDI:
                            NC_000014.9:102891405:C:T
                            Gene:
                            TRAF3 (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)
                            T=0.000007/1 (GnomAD)
                            HGVS:
                            NC_000014.9:g.102891406C>T, NC_000014.8:g.103357743C>T, NG_027973.1:g.118928C>T, NM_003300.4:c.808C>T, NM_003300.3:c.808C>T, NM_145725.3:c.808C>T, NM_145725.2:c.808C>T, NM_145726.3:c.733C>T, NM_145726.2:c.733C>T, NM_001385143.1:c.727C>T, NM_001385142.1:c.808C>T, XM_011537116.4:c.652C>T, XM_011537116.3:c.652C>T, XM_011537116.2:c.652C>T, XM_011537116.1:c.652C>T, XM_017021620.3:c.808C>T, XM_017021620.2:c.808C>T, XM_017021620.1:c.808C>T, XM_017021618.2:c.808C>T, XM_017021618.1:c.808C>T, XM_017021619.2:c.733C>T, XM_017021619.1:c.733C>T, XM_017021617.2:c.808C>T, XM_017021617.1:c.808C>T, XM_047431738.1:c.808C>T, XM_047431739.1:c.733C>T, XM_047431740.1:c.652C>T, NP_003291.2:p.Leu270Phe, NP_663777.1:p.Leu270Phe, NP_663778.1:p.Leu245Phe, NP_001372072.1:p.Leu243Phe, NP_001372071.1:p.Leu270Phe, XP_011535418.1:p.Leu218Phe, XP_016877109.1:p.Leu270Phe, XP_016877107.1:p.Leu270Phe, XP_016877108.1:p.Leu245Phe, XP_016877106.1:p.Leu270Phe, XP_047287694.1:p.Leu270Phe, XP_047287695.1:p.Leu245Phe, XP_047287696.1:p.Leu218Phe

                            14.

                            rs1456863593 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,C [Show Flanks]
                              Chromosome:
                              14:102875668 (GRCh38)
                              14:103342005 (GRCh37)
                              Canonical SPDI:
                              NC_000014.9:102875667:G:A,NC_000014.9:102875667:G:C
                              Gene:
                              TRAF3 (Varview)
                              Functional Consequence:
                              synonymous_variant,missense_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0.000047/1 (ALFA)
                              C=0.000004/1 (GnomAD_exomes)
                              A=0.00006/1 (TOMMO)
                              HGVS:
                              NC_000014.9:g.102875668G>A, NC_000014.9:g.102875668G>C, NC_000014.8:g.103342005G>A, NC_000014.8:g.103342005G>C, NG_027973.1:g.103190G>A, NG_027973.1:g.103190G>C, NM_003300.4:c.342G>A, NM_003300.4:c.342G>C, NM_003300.3:c.342G>A, NM_003300.3:c.342G>C, NM_145725.3:c.342G>A, NM_145725.3:c.342G>C, NM_145725.2:c.342G>A, NM_145725.2:c.342G>C, NM_145726.3:c.342G>A, NM_145726.3:c.342G>C, NM_145726.2:c.342G>A, NM_145726.2:c.342G>C, NM_001199427.2:c.342G>A, NM_001199427.2:c.342G>C, NM_001199427.1:c.342G>A, NM_001199427.1:c.342G>C, NM_001385143.1:c.342G>A, NM_001385143.1:c.342G>C, NM_001385142.1:c.342G>A, NM_001385142.1:c.342G>C, XM_011537116.4:c.342G>A, XM_011537116.4:c.342G>C, XM_011537116.3:c.342G>A, XM_011537116.3:c.342G>C, XM_011537116.2:c.342G>A, XM_011537116.2:c.342G>C, XM_011537116.1:c.342G>A, XM_011537116.1:c.342G>C, XM_011537117.4:c.342G>A, XM_011537117.4:c.342G>C, XM_011537117.3:c.342G>A, XM_011537117.3:c.342G>C, XM_011537117.2:c.342G>A, XM_011537117.2:c.342G>C, XM_011537117.1:c.342G>A, XM_011537117.1:c.342G>C, XM_011537118.4:c.342G>A, XM_011537118.4:c.342G>C, XM_011537118.3:c.342G>A, XM_011537118.3:c.342G>C, XM_011537118.2:c.342G>A, XM_011537118.2:c.342G>C, XM_011537118.1:c.342G>A, XM_011537118.1:c.342G>C, XM_017021620.3:c.342G>A, XM_017021620.3:c.342G>C, XM_017021620.2:c.342G>A, XM_017021620.2:c.342G>C, XM_017021620.1:c.342G>A, XM_017021620.1:c.342G>C, XM_017021618.2:c.342G>A, XM_017021618.2:c.342G>C, XM_017021618.1:c.342G>A, XM_017021618.1:c.342G>C, XM_017021619.2:c.342G>A, XM_017021619.2:c.342G>C, XM_017021619.1:c.342G>A, XM_017021619.1:c.342G>C, XM_017021617.2:c.342G>A, XM_017021617.2:c.342G>C, XM_017021617.1:c.342G>A, XM_017021617.1:c.342G>C, XM_047431741.1:c.342G>A, XM_047431741.1:c.342G>C, XM_047431738.1:c.342G>A, XM_047431738.1:c.342G>C, XM_047431739.1:c.342G>A, XM_047431739.1:c.342G>C, XM_047431740.1:c.342G>A, XM_047431740.1:c.342G>C, XM_047431742.1:c.342G>A, XM_047431742.1:c.342G>C, NP_003291.2:p.Gln114His, NP_663777.1:p.Gln114His, NP_663778.1:p.Gln114His, NP_001186356.1:p.Gln114His, NP_001372072.1:p.Gln114His, NP_001372071.1:p.Gln114His, XP_011535418.1:p.Gln114His, XP_011535419.1:p.Gln114His, XP_011535420.1:p.Gln114His, XP_016877109.1:p.Gln114His, XP_016877107.1:p.Gln114His, XP_016877108.1:p.Gln114His, XP_016877106.1:p.Gln114His, XP_047287697.1:p.Gln114His, XP_047287694.1:p.Gln114His, XP_047287695.1:p.Gln114His, XP_047287696.1:p.Gln114His, XP_047287698.1:p.Gln114His

                              15.

                              rs1451121744 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A,C [Show Flanks]
                                Chromosome:
                                14:102886251 (GRCh38)
                                14:103352588 (GRCh37)
                                Canonical SPDI:
                                NC_000014.9:102886250:G:A,NC_000014.9:102886250:G:C
                                Gene:
                                TRAF3 (Varview)
                                Functional Consequence:
                                intron_variant,coding_sequence_variant,missense_variant,synonymous_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                C=0./0 (ALFA)
                                C=0.000007/1 (GnomAD)
                                C=0.000008/2 (TOPMED)
                                HGVS:
                                NC_000014.9:g.102886251G>A, NC_000014.9:g.102886251G>C, NC_000014.8:g.103352588G>A, NC_000014.8:g.103352588G>C, NG_027973.1:g.113773G>A, NG_027973.1:g.113773G>C, NM_003300.4:c.633G>A, NM_003300.4:c.633G>C, NM_003300.3:c.633G>A, NM_003300.3:c.633G>C, NM_145725.3:c.633G>A, NM_145725.3:c.633G>C, NM_145725.2:c.633G>A, NM_145725.2:c.633G>C, NM_145726.3:c.633G>A, NM_145726.3:c.633G>C, NM_145726.2:c.633G>A, NM_145726.2:c.633G>C, NM_001385142.1:c.633G>A, NM_001385142.1:c.633G>C, XM_011537117.4:c.633G>A, XM_011537117.4:c.633G>C, XM_011537117.3:c.633G>A, XM_011537117.3:c.633G>C, XM_011537117.2:c.633G>A, XM_011537117.2:c.633G>C, XM_011537117.1:c.633G>A, XM_011537117.1:c.633G>C, XM_017021620.3:c.633G>A, XM_017021620.3:c.633G>C, XM_017021620.2:c.633G>A, XM_017021620.2:c.633G>C, XM_017021620.1:c.633G>A, XM_017021620.1:c.633G>C, XM_017021618.2:c.633G>A, XM_017021618.2:c.633G>C, XM_017021618.1:c.633G>A, XM_017021618.1:c.633G>C, XM_017021619.2:c.633G>A, XM_017021619.2:c.633G>C, XM_017021619.1:c.633G>A, XM_017021619.1:c.633G>C, XM_017021617.2:c.633G>A, XM_017021617.2:c.633G>C, XM_017021617.1:c.633G>A, XM_017021617.1:c.633G>C, XM_047431741.1:c.633G>A, XM_047431741.1:c.633G>C, XM_047431738.1:c.633G>A, XM_047431738.1:c.633G>C, XM_047431739.1:c.633G>A, XM_047431739.1:c.633G>C, XM_047431742.1:c.633G>A, XM_047431742.1:c.633G>C, NP_003291.2:p.Gln211His, NP_663777.1:p.Gln211His, NP_663778.1:p.Gln211His, NP_001372071.1:p.Gln211His, XP_011535419.1:p.Gln211His, XP_016877109.1:p.Gln211His, XP_016877107.1:p.Gln211His, XP_016877108.1:p.Gln211His, XP_016877106.1:p.Gln211His, XP_047287697.1:p.Gln211His, XP_047287694.1:p.Gln211His, XP_047287695.1:p.Gln211His, XP_047287698.1:p.Gln211His

                                16.

                                rs1448882419 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  14:102875626 (GRCh38)
                                  14:103341963 (GRCh37)
                                  Canonical SPDI:
                                  NC_000014.9:102875625:G:A
                                  Gene:
                                  TRAF3 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,synonymous_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0./0 (GnomAD)
                                  A=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000014.9:g.102875626G>A, NC_000014.8:g.103341963G>A, NG_027973.1:g.103148G>A, NM_003300.4:c.300G>A, NM_003300.3:c.300G>A, NM_145725.3:c.300G>A, NM_145725.2:c.300G>A, NM_145726.3:c.300G>A, NM_145726.2:c.300G>A, NM_001199427.2:c.300G>A, NM_001199427.1:c.300G>A, NM_001385143.1:c.300G>A, NM_001385142.1:c.300G>A, XM_011537116.4:c.300G>A, XM_011537116.3:c.300G>A, XM_011537116.2:c.300G>A, XM_011537116.1:c.300G>A, XM_011537117.4:c.300G>A, XM_011537117.3:c.300G>A, XM_011537117.2:c.300G>A, XM_011537117.1:c.300G>A, XM_011537118.4:c.300G>A, XM_011537118.3:c.300G>A, XM_011537118.2:c.300G>A, XM_011537118.1:c.300G>A, XM_017021620.3:c.300G>A, XM_017021620.2:c.300G>A, XM_017021620.1:c.300G>A, XM_017021618.2:c.300G>A, XM_017021618.1:c.300G>A, XM_017021619.2:c.300G>A, XM_017021619.1:c.300G>A, XM_017021617.2:c.300G>A, XM_017021617.1:c.300G>A, XM_047431741.1:c.300G>A, XM_047431738.1:c.300G>A, XM_047431739.1:c.300G>A, XM_047431740.1:c.300G>A, XM_047431742.1:c.300G>A

                                  17.

                                  rs1448076918 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    14:102905689 (GRCh38)
                                    14:103372026 (GRCh37)
                                    Canonical SPDI:
                                    NC_000014.9:102905688:G:T
                                    Gene:
                                    TRAF3 (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0.000071/1 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    HGVS:
                                    NC_000014.9:g.102905689G>T, NC_000014.8:g.103372026G>T, NG_027973.1:g.133211G>T, NM_003300.4:c.1612G>T, NM_003300.3:c.1612G>T, NM_145725.3:c.1612G>T, NM_145725.2:c.1612G>T, NM_145726.3:c.1537G>T, NM_145726.2:c.1537G>T, NM_001199427.2:c.1363G>T, NM_001199427.1:c.1363G>T, NM_001385143.1:c.1531G>T, NM_001385142.1:c.1471G>T, XM_011537116.4:c.1456G>T, XM_011537116.3:c.1456G>T, XM_011537116.2:c.1456G>T, XM_011537116.1:c.1456G>T, XM_011537117.4:c.1444G>T, XM_011537117.3:c.1444G>T, XM_011537117.2:c.1444G>T, XM_011537117.1:c.1444G>T, XM_011537118.4:c.1363G>T, XM_011537118.3:c.1363G>T, XM_011537118.2:c.1363G>T, XM_011537118.1:c.1363G>T, XM_017021618.2:c.1612G>T, XM_017021618.1:c.1612G>T, XM_017021619.2:c.1537G>T, XM_017021619.1:c.1537G>T, XM_017021617.2:c.1612G>T, XM_017021617.1:c.1612G>T, XM_047431741.1:c.1444G>T, XM_047431738.1:c.1612G>T, XM_047431739.1:c.1537G>T, XM_047431740.1:c.1456G>T, XM_047431742.1:c.1444G>T, NP_003291.2:p.Val538Leu, NP_663777.1:p.Val538Leu, NP_663778.1:p.Val513Leu, NP_001186356.1:p.Val455Leu, NP_001372072.1:p.Val511Leu, NP_001372071.1:p.Val491Leu, XP_011535418.1:p.Val486Leu, XP_011535419.1:p.Val482Leu, XP_011535420.1:p.Val455Leu, XP_016877107.1:p.Val538Leu, XP_016877108.1:p.Val513Leu, XP_016877106.1:p.Val538Leu, XP_047287697.1:p.Val482Leu, XP_047287694.1:p.Val538Leu, XP_047287695.1:p.Val513Leu, XP_047287696.1:p.Val486Leu, XP_047287698.1:p.Val482Leu

                                    18.

                                    rs1441611359 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      14:102897278 (GRCh38)
                                      14:103363615 (GRCh37)
                                      Canonical SPDI:
                                      NC_000014.9:102897277:T:C
                                      Gene:
                                      TRAF3 (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0.000071/1 (ALFA)
                                      C=0.000014/2 (GnomAD)
                                      C=0.00003/8 (TOPMED)
                                      HGVS:
                                      NC_000014.9:g.102897278T>C, NC_000014.8:g.103363615T>C, NG_027973.1:g.124800T>C, NM_003300.4:c.837T>C, NM_003300.3:c.837T>C, NM_145725.3:c.837T>C, NM_145725.2:c.837T>C, NM_145726.3:c.762T>C, NM_145726.2:c.762T>C, NM_001199427.2:c.588T>C, NM_001199427.1:c.588T>C, NM_001385143.1:c.756T>C, XM_011537116.4:c.681T>C, XM_011537116.3:c.681T>C, XM_011537116.2:c.681T>C, XM_011537116.1:c.681T>C, XM_011537117.4:c.669T>C, XM_011537117.3:c.669T>C, XM_011537117.2:c.669T>C, XM_011537117.1:c.669T>C, XM_011537118.4:c.588T>C, XM_011537118.3:c.588T>C, XM_011537118.2:c.588T>C, XM_011537118.1:c.588T>C, XM_017021618.2:c.837T>C, XM_017021618.1:c.837T>C, XM_017021619.2:c.762T>C, XM_017021619.1:c.762T>C, XM_017021617.2:c.837T>C, XM_017021617.1:c.837T>C, XM_047431741.1:c.669T>C, XM_047431738.1:c.837T>C, XM_047431739.1:c.762T>C, XM_047431740.1:c.681T>C, XM_047431742.1:c.669T>C

                                      19.

                                      rs1440945542 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>A [Show Flanks]
                                        Chromosome:
                                        14:102905538 (GRCh38)
                                        14:103371875 (GRCh37)
                                        Canonical SPDI:
                                        NC_000014.9:102905537:T:A
                                        Gene:
                                        TRAF3 (Varview)
                                        Functional Consequence:
                                        genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000011/3 (TOPMED)
                                        HGVS:
                                        NC_000014.9:g.102905538T>A, NC_000014.8:g.103371875T>A, NG_027973.1:g.133060T>A, NM_003300.4:c.1461T>A, NM_003300.3:c.1461T>A, NM_145725.3:c.1461T>A, NM_145725.2:c.1461T>A, NM_145726.3:c.1386T>A, NM_145726.2:c.1386T>A, NM_001199427.2:c.1212T>A, NM_001199427.1:c.1212T>A, NM_001385143.1:c.1380T>A, NM_001385142.1:c.1320T>A, XM_011537116.4:c.1305T>A, XM_011537116.3:c.1305T>A, XM_011537116.2:c.1305T>A, XM_011537116.1:c.1305T>A, XM_011537117.4:c.1293T>A, XM_011537117.3:c.1293T>A, XM_011537117.2:c.1293T>A, XM_011537117.1:c.1293T>A, XM_011537118.4:c.1212T>A, XM_011537118.3:c.1212T>A, XM_011537118.2:c.1212T>A, XM_011537118.1:c.1212T>A, XM_017021618.2:c.1461T>A, XM_017021618.1:c.1461T>A, XM_017021619.2:c.1386T>A, XM_017021619.1:c.1386T>A, XM_017021617.2:c.1461T>A, XM_017021617.1:c.1461T>A, XM_047431741.1:c.1293T>A, XM_047431738.1:c.1461T>A, XM_047431739.1:c.1386T>A, XM_047431740.1:c.1305T>A, XM_047431742.1:c.1293T>A

                                        20.

                                        rs1440495241 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          14:102876483 (GRCh38)
                                          14:103342820 (GRCh37)
                                          Canonical SPDI:
                                          NC_000014.9:102876482:A:G
                                          Gene:
                                          TRAF3 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant
                                          Clinical significance:
                                          likely-benign
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000004/1 (GnomAD_exomes)
                                          G=0.000004/1 (TOPMED)
                                          HGVS:
                                          NC_000014.9:g.102876483A>G, NC_000014.8:g.103342820A>G, NG_027973.1:g.104005A>G, NM_003300.4:c.528A>G, NM_003300.3:c.528A>G, NM_145725.3:c.528A>G, NM_145725.2:c.528A>G, NM_145726.3:c.528A>G, NM_145726.2:c.528A>G, NM_001199427.2:c.528A>G, NM_001199427.1:c.528A>G, NM_001385143.1:c.528A>G, NM_001385142.1:c.528A>G, XM_011537116.4:c.528A>G, XM_011537116.3:c.528A>G, XM_011537116.2:c.528A>G, XM_011537116.1:c.528A>G, XM_011537117.4:c.528A>G, XM_011537117.3:c.528A>G, XM_011537117.2:c.528A>G, XM_011537117.1:c.528A>G, XM_011537118.4:c.528A>G, XM_011537118.3:c.528A>G, XM_011537118.2:c.528A>G, XM_011537118.1:c.528A>G, XM_017021620.3:c.528A>G, XM_017021620.2:c.528A>G, XM_017021620.1:c.528A>G, XM_017021618.2:c.528A>G, XM_017021618.1:c.528A>G, XM_017021619.2:c.528A>G, XM_017021619.1:c.528A>G, XM_017021617.2:c.528A>G, XM_017021617.1:c.528A>G, XM_047431741.1:c.528A>G, XM_047431738.1:c.528A>G, XM_047431739.1:c.528A>G, XM_047431740.1:c.528A>G, XM_047431742.1:c.528A>G

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