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Items: 1 to 20 of 493

1.

rs1489906607 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C,T [Show Flanks]
    Chromosome:
    17:58734125 (GRCh38)
    17:56811486 (GRCh37)
    Canonical SPDI:
    NC_000017.11:58734124:G:A,NC_000017.11:58734124:G:C,NC_000017.11:58734124:G:T
    Gene:
    RAD51C (Varview), LOC105371843 (Varview)
    Functional Consequence:
    coding_sequence_variant,non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.00003/1 (ALFA)
    HGVS:
    NC_000017.11:g.58734125G>A, NC_000017.11:g.58734125G>C, NC_000017.11:g.58734125G>T, NC_000017.10:g.56811486G>A, NC_000017.10:g.56811486G>C, NC_000017.10:g.56811486G>T, NG_023199.1:g.46524G>A, NG_023199.1:g.46524G>C, NG_023199.1:g.46524G>T, NM_058216.3:c.1034G>A, NM_058216.3:c.1034G>C, NM_058216.3:c.1034G>T, NM_058216.2:c.1034G>A, NM_058216.2:c.1034G>C, NM_058216.2:c.1034G>T, NR_103872.2:n.909G>A, NR_103872.2:n.909G>C, NR_103872.2:n.909G>T, NR_103872.1:n.938G>A, NR_103872.1:n.938G>C, NR_103872.1:n.938G>T, XM_006722001.5:c.1037G>A, XM_006722001.5:c.1037G>C, XM_006722001.5:c.1037G>T, XM_006722001.4:c.1037G>A, XM_006722001.4:c.1037G>C, XM_006722001.4:c.1037G>T, XM_006722001.3:c.1037G>A, XM_006722001.3:c.1037G>C, XM_006722001.3:c.1037G>T, XM_006722001.2:c.1037G>A, XM_006722001.2:c.1037G>C, XM_006722001.2:c.1037G>T, XM_006722001.1:c.1037G>A, XM_006722001.1:c.1037G>C, XM_006722001.1:c.1037G>T, XM_006722002.5:c.973G>A, XM_006722002.5:c.973G>C, XM_006722002.5:c.973G>T, XM_006722002.4:c.973G>A, XM_006722002.4:c.973G>C, XM_006722002.4:c.973G>T, XM_006722002.3:c.973G>A, XM_006722002.3:c.973G>C, XM_006722002.3:c.973G>T, XM_006722002.2:c.973G>A, XM_006722002.2:c.973G>C, XM_006722002.2:c.973G>T, XM_006722002.1:c.973G>A, XM_006722002.1:c.973G>C, XM_006722002.1:c.973G>T, XM_006722004.4:c.686G>A, XM_006722004.4:c.686G>C, XM_006722004.4:c.686G>T, XM_006722004.3:c.686G>A, XM_006722004.3:c.686G>C, XM_006722004.3:c.686G>T, XM_006722004.2:c.686G>A, XM_006722004.2:c.686G>C, XM_006722004.2:c.686G>T, XM_006722004.1:c.686G>A, XM_006722004.1:c.686G>C, XM_006722004.1:c.686G>T, XM_011525094.3:c.686G>A, XM_011525094.3:c.686G>C, XM_011525094.3:c.686G>T, XM_011525094.2:c.686G>A, XM_011525094.2:c.686G>C, XM_011525094.2:c.686G>T, XM_011525094.1:c.686G>A, XM_011525094.1:c.686G>C, XM_011525094.1:c.686G>T, NM_058217.1:c.*462G>A, NM_058217.1:c.*462G>C, NM_058217.1:c.*462G>T, NP_478123.1:p.Gly345Glu, NP_478123.1:p.Gly345Ala, NP_478123.1:p.Gly345Val, XP_006722064.1:p.Gly346Glu, XP_006722064.1:p.Gly346Ala, XP_006722064.1:p.Gly346Val, XP_006722065.1:p.Asp325Asn, XP_006722065.1:p.Asp325His, XP_006722065.1:p.Asp325Tyr, XP_006722067.1:p.Gly229Glu, XP_006722067.1:p.Gly229Ala, XP_006722067.1:p.Gly229Val, XP_011523396.1:p.Gly229Glu, XP_011523396.1:p.Gly229Ala, XP_011523396.1:p.Gly229Val

    2.

    rs1486574276 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A,C [Show Flanks]
      Chromosome:
      17:58696795 (GRCh38)
      17:56774156 (GRCh37)
      Canonical SPDI:
      NC_000017.11:58696794:G:A,NC_000017.11:58696794:G:C
      Gene:
      RAD51C (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant,intron_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_000017.11:g.58696795G>A, NC_000017.11:g.58696795G>C, NC_000017.10:g.56774156G>A, NC_000017.10:g.56774156G>C, NG_047169.1:g.285C>T, NG_047169.1:g.285C>G, NG_023199.1:g.9194G>A, NG_023199.1:g.9194G>C, NM_058216.3:c.507G>A, NM_058216.3:c.507G>C, NM_058216.2:c.507G>A, NM_058216.2:c.507G>C, XM_006722001.5:c.507G>A, XM_006722001.5:c.507G>C, XM_006722001.4:c.507G>A, XM_006722001.4:c.507G>C, XM_006722001.3:c.507G>A, XM_006722001.3:c.507G>C, XM_006722001.2:c.507G>A, XM_006722001.2:c.507G>C, XM_006722001.1:c.507G>A, XM_006722001.1:c.507G>C, XM_006722002.5:c.507G>A, XM_006722002.5:c.507G>C, XM_006722002.4:c.507G>A, XM_006722002.4:c.507G>C, XM_006722002.3:c.507G>A, XM_006722002.3:c.507G>C, XM_006722002.2:c.507G>A, XM_006722002.2:c.507G>C, XM_006722002.1:c.507G>A, XM_006722002.1:c.507G>C, XM_006722004.4:c.156G>A, XM_006722004.4:c.156G>C, XM_006722004.3:c.156G>A, XM_006722004.3:c.156G>C, XM_006722004.2:c.156G>A, XM_006722004.2:c.156G>C, XM_006722004.1:c.156G>A, XM_006722004.1:c.156G>C, XM_011525094.3:c.156G>A, XM_011525094.3:c.156G>C, XM_011525094.2:c.156G>A, XM_011525094.2:c.156G>C, XM_011525094.1:c.156G>A, XM_011525094.1:c.156G>C, XM_047436505.1:c.507G>A, XM_047436505.1:c.507G>C

      3.

      rs1484551212 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>A,G,T [Show Flanks]
        Chromosome:
        17:58695094 (GRCh38)
        17:56772455 (GRCh37)
        Canonical SPDI:
        NC_000017.11:58695093:C:A,NC_000017.11:58695093:C:G,NC_000017.11:58695093:C:T
        Gene:
        RAD51C (Varview)
        Functional Consequence:
        coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant,synonymous_variant,missense_variant
        Clinical significance:
        uncertain-significance
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        HGVS:
        NC_000017.11:g.58695094C>A, NC_000017.11:g.58695094C>G, NC_000017.11:g.58695094C>T, NC_000017.10:g.56772455C>A, NC_000017.10:g.56772455C>G, NC_000017.10:g.56772455C>T, NG_047169.1:g.1986G>T, NG_047169.1:g.1986G>C, NG_047169.1:g.1986G>A, NG_023199.1:g.7493C>A, NG_023199.1:g.7493C>G, NG_023199.1:g.7493C>T, NM_002876.4:c.309C>A, NM_002876.4:c.309C>G, NM_002876.4:c.309C>T, NM_002876.3:c.309C>A, NM_002876.3:c.309C>G, NM_002876.3:c.309C>T, NM_058216.3:c.309C>A, NM_058216.3:c.309C>G, NM_058216.3:c.309C>T, NM_058216.2:c.309C>A, NM_058216.2:c.309C>G, NM_058216.2:c.309C>T, NR_103872.2:n.351C>A, NR_103872.2:n.351C>G, NR_103872.2:n.351C>T, NR_103872.1:n.380C>A, NR_103872.1:n.380C>G, NR_103872.1:n.380C>T, NR_103873.1:n.277C>A, NR_103873.1:n.277C>G, NR_103873.1:n.277C>T, XM_006722001.5:c.309C>A, XM_006722001.5:c.309C>G, XM_006722001.5:c.309C>T, XM_006722001.4:c.309C>A, XM_006722001.4:c.309C>G, XM_006722001.4:c.309C>T, XM_006722001.3:c.309C>A, XM_006722001.3:c.309C>G, XM_006722001.3:c.309C>T, XM_006722001.2:c.309C>A, XM_006722001.2:c.309C>G, XM_006722001.2:c.309C>T, XM_006722001.1:c.309C>A, XM_006722001.1:c.309C>G, XM_006722001.1:c.309C>T, XM_006722002.5:c.309C>A, XM_006722002.5:c.309C>G, XM_006722002.5:c.309C>T, XM_006722002.4:c.309C>A, XM_006722002.4:c.309C>G, XM_006722002.4:c.309C>T, XM_006722002.3:c.309C>A, XM_006722002.3:c.309C>G, XM_006722002.3:c.309C>T, XM_006722002.2:c.309C>A, XM_006722002.2:c.309C>G, XM_006722002.2:c.309C>T, XM_006722002.1:c.309C>A, XM_006722002.1:c.309C>G, XM_006722002.1:c.309C>T, XM_006722004.4:c.-43C>A, XM_006722004.4:c.-43C>G, XM_006722004.4:c.-43C>T, XM_006722004.3:c.-43C>A, XM_006722004.3:c.-43C>G, XM_006722004.3:c.-43C>T, XM_006722004.2:c.-43C>A, XM_006722004.2:c.-43C>G, XM_006722004.2:c.-43C>T, XM_006722004.1:c.-43C>A, XM_006722004.1:c.-43C>G, XM_006722004.1:c.-43C>T, XM_011525094.3:c.-43C>A, XM_011525094.3:c.-43C>G, XM_011525094.3:c.-43C>T, XM_011525094.2:c.-43C>A, XM_011525094.2:c.-43C>G, XM_011525094.2:c.-43C>T, XM_011525094.1:c.-43C>A, XM_011525094.1:c.-43C>G, XM_011525094.1:c.-43C>T, NM_058217.1:c.309C>A, NM_058217.1:c.309C>G, NM_058217.1:c.309C>T, XM_047436505.1:c.309C>A, XM_047436505.1:c.309C>G, XM_047436505.1:c.309C>T, NP_002867.1:p.Phe103Leu, NP_002867.1:p.Phe103Leu, NP_478123.1:p.Phe103Leu, NP_478123.1:p.Phe103Leu, XP_006722064.1:p.Phe103Leu, XP_006722064.1:p.Phe103Leu, XP_006722065.1:p.Phe103Leu, XP_006722065.1:p.Phe103Leu, XP_047292461.1:p.Phe103Leu, XP_047292461.1:p.Phe103Leu

        4.

        rs1483938000 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G,T [Show Flanks]
          Chromosome:
          17:58703268 (GRCh38)
          17:56780629 (GRCh37)
          Canonical SPDI:
          NC_000017.11:58703267:A:G,NC_000017.11:58703267:A:T
          Gene:
          RAD51C (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,missense_variant
          Clinical significance:
          uncertain-significance
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0./0 (ALFA)
          G=0.000004/1 (GnomAD_exomes)
          G=0.000004/1 (TOPMED)
          G=0.000007/1 (GnomAD)
          HGVS:
          NC_000017.11:g.58703268A>G, NC_000017.11:g.58703268A>T, NC_000017.10:g.56780629A>G, NC_000017.10:g.56780629A>T, NG_023199.1:g.15667A>G, NG_023199.1:g.15667A>T, NM_058216.3:c.644A>G, NM_058216.3:c.644A>T, NM_058216.2:c.644A>G, NM_058216.2:c.644A>T, NR_103872.2:n.519A>G, NR_103872.2:n.519A>T, NR_103872.1:n.548A>G, NR_103872.1:n.548A>T, XM_006722001.5:c.644A>G, XM_006722001.5:c.644A>T, XM_006722001.4:c.644A>G, XM_006722001.4:c.644A>T, XM_006722001.3:c.644A>G, XM_006722001.3:c.644A>T, XM_006722001.2:c.644A>G, XM_006722001.2:c.644A>T, XM_006722001.1:c.644A>G, XM_006722001.1:c.644A>T, XM_006722002.5:c.644A>G, XM_006722002.5:c.644A>T, XM_006722002.4:c.644A>G, XM_006722002.4:c.644A>T, XM_006722002.3:c.644A>G, XM_006722002.3:c.644A>T, XM_006722002.2:c.644A>G, XM_006722002.2:c.644A>T, XM_006722002.1:c.644A>G, XM_006722002.1:c.644A>T, XM_006722004.4:c.293A>G, XM_006722004.4:c.293A>T, XM_006722004.3:c.293A>G, XM_006722004.3:c.293A>T, XM_006722004.2:c.293A>G, XM_006722004.2:c.293A>T, XM_006722004.1:c.293A>G, XM_006722004.1:c.293A>T, XM_011525094.3:c.293A>G, XM_011525094.3:c.293A>T, XM_011525094.2:c.293A>G, XM_011525094.2:c.293A>T, XM_011525094.1:c.293A>G, XM_011525094.1:c.293A>T, NM_058217.1:c.*72A>G, NM_058217.1:c.*72A>T, XM_047436505.1:c.644A>G, XM_047436505.1:c.644A>T, NP_478123.1:p.Asp215Gly, NP_478123.1:p.Asp215Val, XP_006722064.1:p.Asp215Gly, XP_006722064.1:p.Asp215Val, XP_006722065.1:p.Asp215Gly, XP_006722065.1:p.Asp215Val, XP_006722067.1:p.Asp98Gly, XP_006722067.1:p.Asp98Val, XP_011523396.1:p.Asp98Gly, XP_011523396.1:p.Asp98Val, XP_047292461.1:p.Asp215Gly, XP_047292461.1:p.Asp215Val

          5.

          rs1481957875 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A,G,T [Show Flanks]
            Chromosome:
            17:58703260 (GRCh38)
            17:56780621 (GRCh37)
            Canonical SPDI:
            NC_000017.11:58703259:C:A,NC_000017.11:58703259:C:G,NC_000017.11:58703259:C:T
            Gene:
            RAD51C (Varview)
            Functional Consequence:
            genic_downstream_transcript_variant,synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
            Clinical significance:
            likely-benign
            Validated:
            by frequency,by cluster
            MAF:
            T=0.000004/1 (GnomAD_exomes)
            T=0.000342/1 (KOREAN)
            HGVS:
            NC_000017.11:g.58703260C>A, NC_000017.11:g.58703260C>G, NC_000017.11:g.58703260C>T, NC_000017.10:g.56780621C>A, NC_000017.10:g.56780621C>G, NC_000017.10:g.56780621C>T, NG_023199.1:g.15659C>A, NG_023199.1:g.15659C>G, NG_023199.1:g.15659C>T, NM_058216.3:c.636C>A, NM_058216.3:c.636C>G, NM_058216.3:c.636C>T, NM_058216.2:c.636C>A, NM_058216.2:c.636C>G, NM_058216.2:c.636C>T, NR_103872.2:n.511C>A, NR_103872.2:n.511C>G, NR_103872.2:n.511C>T, NR_103872.1:n.540C>A, NR_103872.1:n.540C>G, NR_103872.1:n.540C>T, XM_006722001.5:c.636C>A, XM_006722001.5:c.636C>G, XM_006722001.5:c.636C>T, XM_006722001.4:c.636C>A, XM_006722001.4:c.636C>G, XM_006722001.4:c.636C>T, XM_006722001.3:c.636C>A, XM_006722001.3:c.636C>G, XM_006722001.3:c.636C>T, XM_006722001.2:c.636C>A, XM_006722001.2:c.636C>G, XM_006722001.2:c.636C>T, XM_006722001.1:c.636C>A, XM_006722001.1:c.636C>G, XM_006722001.1:c.636C>T, XM_006722002.5:c.636C>A, XM_006722002.5:c.636C>G, XM_006722002.5:c.636C>T, XM_006722002.4:c.636C>A, XM_006722002.4:c.636C>G, XM_006722002.4:c.636C>T, XM_006722002.3:c.636C>A, XM_006722002.3:c.636C>G, XM_006722002.3:c.636C>T, XM_006722002.2:c.636C>A, XM_006722002.2:c.636C>G, XM_006722002.2:c.636C>T, XM_006722002.1:c.636C>A, XM_006722002.1:c.636C>G, XM_006722002.1:c.636C>T, XM_006722004.4:c.285C>A, XM_006722004.4:c.285C>G, XM_006722004.4:c.285C>T, XM_006722004.3:c.285C>A, XM_006722004.3:c.285C>G, XM_006722004.3:c.285C>T, XM_006722004.2:c.285C>A, XM_006722004.2:c.285C>G, XM_006722004.2:c.285C>T, XM_006722004.1:c.285C>A, XM_006722004.1:c.285C>G, XM_006722004.1:c.285C>T, XM_011525094.3:c.285C>A, XM_011525094.3:c.285C>G, XM_011525094.3:c.285C>T, XM_011525094.2:c.285C>A, XM_011525094.2:c.285C>G, XM_011525094.2:c.285C>T, XM_011525094.1:c.285C>A, XM_011525094.1:c.285C>G, XM_011525094.1:c.285C>T, NM_058217.1:c.*64C>A, NM_058217.1:c.*64C>G, NM_058217.1:c.*64C>T, XM_047436505.1:c.636C>A, XM_047436505.1:c.636C>G, XM_047436505.1:c.636C>T

            6.

            rs1479360028 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              CTTTCAT>- [Show Flanks]
              Chromosome:
              17:58724077 (GRCh38)
              17:56801438 (GRCh37)
              Canonical SPDI:
              NC_000017.11:58724074:ATCTTTCAT:AT
              Gene:
              RAD51C (Varview), LOC105371843 (Varview)
              Functional Consequence:
              frameshift_variant,coding_sequence_variant,downstream_transcript_variant,500B_downstream_variant,non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
              Validated:
              by frequency
              MAF:
              -=0.000004/1 (GnomAD_exomes)
              HGVS:

              7.

              rs1476282276 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A,G [Show Flanks]
                Chromosome:
                17:58696834 (GRCh38)
                17:56774195 (GRCh37)
                Canonical SPDI:
                NC_000017.11:58696833:T:A,NC_000017.11:58696833:T:G
                Gene:
                RAD51C (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
                Clinical significance:
                likely-benign
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                G=0./0 (ALFA)
                G=0.000019/5 (TOPMED)
                G=0.000036/5 (GnomAD)
                HGVS:
                NC_000017.11:g.58696834T>A, NC_000017.11:g.58696834T>G, NC_000017.10:g.56774195T>A, NC_000017.10:g.56774195T>G, NG_047169.1:g.246A>T, NG_047169.1:g.246A>C, NG_023199.1:g.9233T>A, NG_023199.1:g.9233T>G, NM_058216.3:c.546T>A, NM_058216.3:c.546T>G, NM_058216.2:c.546T>A, NM_058216.2:c.546T>G, XM_006722001.5:c.546T>A, XM_006722001.5:c.546T>G, XM_006722001.4:c.546T>A, XM_006722001.4:c.546T>G, XM_006722001.3:c.546T>A, XM_006722001.3:c.546T>G, XM_006722001.2:c.546T>A, XM_006722001.2:c.546T>G, XM_006722001.1:c.546T>A, XM_006722001.1:c.546T>G, XM_006722002.5:c.546T>A, XM_006722002.5:c.546T>G, XM_006722002.4:c.546T>A, XM_006722002.4:c.546T>G, XM_006722002.3:c.546T>A, XM_006722002.3:c.546T>G, XM_006722002.2:c.546T>A, XM_006722002.2:c.546T>G, XM_006722002.1:c.546T>A, XM_006722002.1:c.546T>G, XM_006722004.4:c.195T>A, XM_006722004.4:c.195T>G, XM_006722004.3:c.195T>A, XM_006722004.3:c.195T>G, XM_006722004.2:c.195T>A, XM_006722004.2:c.195T>G, XM_006722004.1:c.195T>A, XM_006722004.1:c.195T>G, XM_011525094.3:c.195T>A, XM_011525094.3:c.195T>G, XM_011525094.2:c.195T>A, XM_011525094.2:c.195T>G, XM_011525094.1:c.195T>A, XM_011525094.1:c.195T>G, XM_047436505.1:c.546T>A, XM_047436505.1:c.546T>G

                8.

                rs1473651696 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A,C,T [Show Flanks]
                  Chromosome:
                  17:58734139 (GRCh38)
                  17:56811500 (GRCh37)
                  Canonical SPDI:
                  NC_000017.11:58734138:G:A,NC_000017.11:58734138:G:C,NC_000017.11:58734138:G:T
                  Gene:
                  RAD51C (Varview), LOC105371843 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant,synonymous_variant,missense_variant
                  Clinical significance:
                  uncertain-significance
                  Validated:
                  by frequency,by cluster
                  MAF:
                  C=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000017.11:g.58734139G>A, NC_000017.11:g.58734139G>C, NC_000017.11:g.58734139G>T, NC_000017.10:g.56811500G>A, NC_000017.10:g.56811500G>C, NC_000017.10:g.56811500G>T, NG_023199.1:g.46538G>A, NG_023199.1:g.46538G>C, NG_023199.1:g.46538G>T, NM_058216.3:c.1048G>A, NM_058216.3:c.1048G>C, NM_058216.3:c.1048G>T, NM_058216.2:c.1048G>A, NM_058216.2:c.1048G>C, NM_058216.2:c.1048G>T, NR_103872.2:n.923G>A, NR_103872.2:n.923G>C, NR_103872.2:n.923G>T, NR_103872.1:n.952G>A, NR_103872.1:n.952G>C, NR_103872.1:n.952G>T, XM_006722001.5:c.1051G>A, XM_006722001.5:c.1051G>C, XM_006722001.5:c.1051G>T, XM_006722001.4:c.1051G>A, XM_006722001.4:c.1051G>C, XM_006722001.4:c.1051G>T, XM_006722001.3:c.1051G>A, XM_006722001.3:c.1051G>C, XM_006722001.3:c.1051G>T, XM_006722001.2:c.1051G>A, XM_006722001.2:c.1051G>C, XM_006722001.2:c.1051G>T, XM_006722001.1:c.1051G>A, XM_006722001.1:c.1051G>C, XM_006722001.1:c.1051G>T, XM_006722002.5:c.987G>A, XM_006722002.5:c.987G>C, XM_006722002.5:c.987G>T, XM_006722002.4:c.987G>A, XM_006722002.4:c.987G>C, XM_006722002.4:c.987G>T, XM_006722002.3:c.987G>A, XM_006722002.3:c.987G>C, XM_006722002.3:c.987G>T, XM_006722002.2:c.987G>A, XM_006722002.2:c.987G>C, XM_006722002.2:c.987G>T, XM_006722002.1:c.987G>A, XM_006722002.1:c.987G>C, XM_006722002.1:c.987G>T, XM_006722004.4:c.700G>A, XM_006722004.4:c.700G>C, XM_006722004.4:c.700G>T, XM_006722004.3:c.700G>A, XM_006722004.3:c.700G>C, XM_006722004.3:c.700G>T, XM_006722004.2:c.700G>A, XM_006722004.2:c.700G>C, XM_006722004.2:c.700G>T, XM_006722004.1:c.700G>A, XM_006722004.1:c.700G>C, XM_006722004.1:c.700G>T, XM_011525094.3:c.700G>A, XM_011525094.3:c.700G>C, XM_011525094.3:c.700G>T, XM_011525094.2:c.700G>A, XM_011525094.2:c.700G>C, XM_011525094.2:c.700G>T, XM_011525094.1:c.700G>A, XM_011525094.1:c.700G>C, XM_011525094.1:c.700G>T, NM_058217.1:c.*476G>A, NM_058217.1:c.*476G>C, NM_058217.1:c.*476G>T, NP_478123.1:p.Val350Ile, NP_478123.1:p.Val350Leu, NP_478123.1:p.Val350Phe, XP_006722064.1:p.Val351Ile, XP_006722064.1:p.Val351Leu, XP_006722064.1:p.Val351Phe, XP_006722067.1:p.Val234Ile, XP_006722067.1:p.Val234Leu, XP_006722067.1:p.Val234Phe, XP_011523396.1:p.Val234Ile, XP_011523396.1:p.Val234Leu, XP_011523396.1:p.Val234Phe

                  9.

                  rs1466185247 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    A>- [Show Flanks]
                    Chromosome:
                    17:58709972 (GRCh38)
                    17:56787333 (GRCh37)
                    Canonical SPDI:
                    NC_000017.11:58709971:AAA:AA
                    Gene:
                    RAD51C (Varview)
                    Functional Consequence:
                    genic_downstream_transcript_variant,frameshift_variant,non_coding_transcript_variant,coding_sequence_variant
                    Clinical significance:
                    pathogenic
                    Validated:
                    by frequency
                    MAF:
                    -=0.000004/1 (GnomAD_exomes)
                    HGVS:

                    10.

                    rs1463646629 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,C,T [Show Flanks]
                      Chromosome:
                      17:58696791 (GRCh38)
                      17:56774152 (GRCh37)
                      Canonical SPDI:
                      NC_000017.11:58696790:G:A,NC_000017.11:58696790:G:C,NC_000017.11:58696790:G:T
                      Gene:
                      RAD51C (Varview)
                      Functional Consequence:
                      genic_downstream_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000017.11:g.58696791G>A, NC_000017.11:g.58696791G>C, NC_000017.11:g.58696791G>T, NC_000017.10:g.56774152G>A, NC_000017.10:g.56774152G>C, NC_000017.10:g.56774152G>T, NG_047169.1:g.289C>T, NG_047169.1:g.289C>G, NG_047169.1:g.289C>A, NG_023199.1:g.9190G>A, NG_023199.1:g.9190G>C, NG_023199.1:g.9190G>T, NM_058216.3:c.503G>A, NM_058216.3:c.503G>C, NM_058216.3:c.503G>T, NM_058216.2:c.503G>A, NM_058216.2:c.503G>C, NM_058216.2:c.503G>T, XM_006722001.5:c.503G>A, XM_006722001.5:c.503G>C, XM_006722001.5:c.503G>T, XM_006722001.4:c.503G>A, XM_006722001.4:c.503G>C, XM_006722001.4:c.503G>T, XM_006722001.3:c.503G>A, XM_006722001.3:c.503G>C, XM_006722001.3:c.503G>T, XM_006722001.2:c.503G>A, XM_006722001.2:c.503G>C, XM_006722001.2:c.503G>T, XM_006722001.1:c.503G>A, XM_006722001.1:c.503G>C, XM_006722001.1:c.503G>T, XM_006722002.5:c.503G>A, XM_006722002.5:c.503G>C, XM_006722002.5:c.503G>T, XM_006722002.4:c.503G>A, XM_006722002.4:c.503G>C, XM_006722002.4:c.503G>T, XM_006722002.3:c.503G>A, XM_006722002.3:c.503G>C, XM_006722002.3:c.503G>T, XM_006722002.2:c.503G>A, XM_006722002.2:c.503G>C, XM_006722002.2:c.503G>T, XM_006722002.1:c.503G>A, XM_006722002.1:c.503G>C, XM_006722002.1:c.503G>T, XM_006722004.4:c.152G>A, XM_006722004.4:c.152G>C, XM_006722004.4:c.152G>T, XM_006722004.3:c.152G>A, XM_006722004.3:c.152G>C, XM_006722004.3:c.152G>T, XM_006722004.2:c.152G>A, XM_006722004.2:c.152G>C, XM_006722004.2:c.152G>T, XM_006722004.1:c.152G>A, XM_006722004.1:c.152G>C, XM_006722004.1:c.152G>T, XM_011525094.3:c.152G>A, XM_011525094.3:c.152G>C, XM_011525094.3:c.152G>T, XM_011525094.2:c.152G>A, XM_011525094.2:c.152G>C, XM_011525094.2:c.152G>T, XM_011525094.1:c.152G>A, XM_011525094.1:c.152G>C, XM_011525094.1:c.152G>T, XM_047436505.1:c.503G>A, XM_047436505.1:c.503G>C, XM_047436505.1:c.503G>T, NP_478123.1:p.Arg168Lys, NP_478123.1:p.Arg168Thr, NP_478123.1:p.Arg168Ile, XP_006722064.1:p.Arg168Lys, XP_006722064.1:p.Arg168Thr, XP_006722064.1:p.Arg168Ile, XP_006722065.1:p.Arg168Lys, XP_006722065.1:p.Arg168Thr, XP_006722065.1:p.Arg168Ile, XP_006722067.1:p.Arg51Lys, XP_006722067.1:p.Arg51Thr, XP_006722067.1:p.Arg51Ile, XP_011523396.1:p.Arg51Lys, XP_011523396.1:p.Arg51Thr, XP_011523396.1:p.Arg51Ile, XP_047292461.1:p.Arg168Lys, XP_047292461.1:p.Arg168Thr, XP_047292461.1:p.Arg168Ile

                      11.

                      rs1462774351 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        17:58703215 (GRCh38)
                        17:56780576 (GRCh37)
                        Canonical SPDI:
                        NC_000017.11:58703214:G:A
                        Gene:
                        RAD51C (Varview)
                        Functional Consequence:
                        genic_downstream_transcript_variant,synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
                        Validated:
                        by frequency,by cluster
                        MAF:
                        A=0.000004/1 (GnomAD_exomes)
                        HGVS:

                        12.

                        rs1460932618 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C,T [Show Flanks]
                          Chromosome:
                          17:58709933 (GRCh38)
                          17:56787294 (GRCh37)
                          Canonical SPDI:
                          NC_000017.11:58709932:G:A,NC_000017.11:58709932:G:C,NC_000017.11:58709932:G:T
                          Gene:
                          RAD51C (Varview)
                          Functional Consequence:
                          genic_downstream_transcript_variant,synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
                          Clinical significance:
                          likely-benign
                          Validated:
                          by cluster
                          HGVS:
                          NC_000017.11:g.58709933G>A, NC_000017.11:g.58709933G>C, NC_000017.11:g.58709933G>T, NC_000017.10:g.56787294G>A, NC_000017.10:g.56787294G>C, NC_000017.10:g.56787294G>T, NG_023199.1:g.22332G>A, NG_023199.1:g.22332G>C, NG_023199.1:g.22332G>T, NM_058216.3:c.780G>A, NM_058216.3:c.780G>C, NM_058216.3:c.780G>T, NM_058216.2:c.780G>A, NM_058216.2:c.780G>C, NM_058216.2:c.780G>T, NR_103872.2:n.655G>A, NR_103872.2:n.655G>C, NR_103872.2:n.655G>T, NR_103872.1:n.684G>A, NR_103872.1:n.684G>C, NR_103872.1:n.684G>T, XM_006722001.5:c.780G>A, XM_006722001.5:c.780G>C, XM_006722001.5:c.780G>T, XM_006722001.4:c.780G>A, XM_006722001.4:c.780G>C, XM_006722001.4:c.780G>T, XM_006722001.3:c.780G>A, XM_006722001.3:c.780G>C, XM_006722001.3:c.780G>T, XM_006722001.2:c.780G>A, XM_006722001.2:c.780G>C, XM_006722001.2:c.780G>T, XM_006722001.1:c.780G>A, XM_006722001.1:c.780G>C, XM_006722001.1:c.780G>T, XM_006722002.5:c.780G>A, XM_006722002.5:c.780G>C, XM_006722002.5:c.780G>T, XM_006722002.4:c.780G>A, XM_006722002.4:c.780G>C, XM_006722002.4:c.780G>T, XM_006722002.3:c.780G>A, XM_006722002.3:c.780G>C, XM_006722002.3:c.780G>T, XM_006722002.2:c.780G>A, XM_006722002.2:c.780G>C, XM_006722002.2:c.780G>T, XM_006722002.1:c.780G>A, XM_006722002.1:c.780G>C, XM_006722002.1:c.780G>T, XM_006722004.4:c.429G>A, XM_006722004.4:c.429G>C, XM_006722004.4:c.429G>T, XM_006722004.3:c.429G>A, XM_006722004.3:c.429G>C, XM_006722004.3:c.429G>T, XM_006722004.2:c.429G>A, XM_006722004.2:c.429G>C, XM_006722004.2:c.429G>T, XM_006722004.1:c.429G>A, XM_006722004.1:c.429G>C, XM_006722004.1:c.429G>T, XM_011525094.3:c.429G>A, XM_011525094.3:c.429G>C, XM_011525094.3:c.429G>T, XM_011525094.2:c.429G>A, XM_011525094.2:c.429G>C, XM_011525094.2:c.429G>T, XM_011525094.1:c.429G>A, XM_011525094.1:c.429G>C, XM_011525094.1:c.429G>T, NM_058217.1:c.*208G>A, NM_058217.1:c.*208G>C, NM_058217.1:c.*208G>T

                          13.

                          rs1452865935 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G,T [Show Flanks]
                            Chromosome:
                            17:58692671 (GRCh38)
                            17:56770032 (GRCh37)
                            Canonical SPDI:
                            NC_000017.11:58692670:A:G,NC_000017.11:58692670:A:T
                            Gene:
                            RAD51C (Varview), TEX14 (Varview), IGBP1P2 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
                            Clinical significance:
                            uncertain-significance
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000014/2 (GnomAD)
                            T=0.000015/4 (TOPMED)
                            HGVS:
                            NC_000017.11:g.58692671A>G, NC_000017.11:g.58692671A>T, NC_000017.10:g.56770032A>G, NC_000017.10:g.56770032A>T, NG_047169.1:g.4409T>C, NG_047169.1:g.4409T>A, NG_023199.1:g.5070A>G, NG_023199.1:g.5070A>T, NM_002876.4:c.28A>G, NM_002876.4:c.28A>T, NM_002876.3:c.28A>G, NM_002876.3:c.28A>T, NM_058216.3:c.28A>G, NM_058216.3:c.28A>T, NM_058216.2:c.28A>G, NM_058216.2:c.28A>T, NR_103872.2:n.70A>G, NR_103872.2:n.70A>T, NR_103872.1:n.99A>G, NR_103872.1:n.99A>T, NR_103873.1:n.99A>G, NR_103873.1:n.99A>T, XM_006722001.5:c.28A>G, XM_006722001.5:c.28A>T, XM_006722001.4:c.28A>G, XM_006722001.4:c.28A>T, XM_006722001.3:c.28A>G, XM_006722001.3:c.28A>T, XM_006722001.2:c.28A>G, XM_006722001.2:c.28A>T, XM_006722001.1:c.28A>G, XM_006722001.1:c.28A>T, XM_006722002.5:c.28A>G, XM_006722002.5:c.28A>T, XM_006722002.4:c.28A>G, XM_006722002.4:c.28A>T, XM_006722002.3:c.28A>G, XM_006722002.3:c.28A>T, XM_006722002.2:c.28A>G, XM_006722002.2:c.28A>T, XM_006722002.1:c.28A>G, XM_006722002.1:c.28A>T, XM_006722004.4:c.-221A>G, XM_006722004.4:c.-221A>T, XM_006722004.3:c.-221A>G, XM_006722004.3:c.-221A>T, XM_006722004.2:c.-221A>G, XM_006722004.2:c.-221A>T, XM_006722004.1:c.-221A>G, XM_006722004.1:c.-221A>T, NM_058217.1:c.28A>G, NM_058217.1:c.28A>T, XM_047436505.1:c.28A>G, XM_047436505.1:c.28A>T, NP_002867.1:p.Met10Val, NP_002867.1:p.Met10Leu, NP_478123.1:p.Met10Val, NP_478123.1:p.Met10Leu, XP_006722064.1:p.Met10Val, XP_006722064.1:p.Met10Leu, XP_006722065.1:p.Met10Val, XP_006722065.1:p.Met10Leu, XP_047292461.1:p.Met10Val, XP_047292461.1:p.Met10Leu

                            14.

                            rs1449359018 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,C,T [Show Flanks]
                              Chromosome:
                              17:58695015 (GRCh38)
                              17:56772376 (GRCh37)
                              Canonical SPDI:
                              NC_000017.11:58695014:G:A,NC_000017.11:58695014:G:C,NC_000017.11:58695014:G:T
                              Gene:
                              RAD51C (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant,5_prime_UTR_variant,missense_variant,coding_sequence_variant
                              Clinical significance:
                              uncertain-significance
                              Validated:
                              by frequency,by cluster
                              MAF:
                              C=0.000004/1 (GnomAD_exomes)
                              HGVS:
                              NC_000017.11:g.58695015G>A, NC_000017.11:g.58695015G>C, NC_000017.11:g.58695015G>T, NC_000017.10:g.56772376G>A, NC_000017.10:g.56772376G>C, NC_000017.10:g.56772376G>T, NG_047169.1:g.2065C>T, NG_047169.1:g.2065C>G, NG_047169.1:g.2065C>A, NG_023199.1:g.7414G>A, NG_023199.1:g.7414G>C, NG_023199.1:g.7414G>T, NM_002876.4:c.230G>A, NM_002876.4:c.230G>C, NM_002876.4:c.230G>T, NM_002876.3:c.230G>A, NM_002876.3:c.230G>C, NM_002876.3:c.230G>T, NM_058216.3:c.230G>A, NM_058216.3:c.230G>C, NM_058216.3:c.230G>T, NM_058216.2:c.230G>A, NM_058216.2:c.230G>C, NM_058216.2:c.230G>T, NR_103872.2:n.272G>A, NR_103872.2:n.272G>C, NR_103872.2:n.272G>T, NR_103872.1:n.301G>A, NR_103872.1:n.301G>C, NR_103872.1:n.301G>T, NR_103873.1:n.198G>A, NR_103873.1:n.198G>C, NR_103873.1:n.198G>T, XM_006722001.5:c.230G>A, XM_006722001.5:c.230G>C, XM_006722001.5:c.230G>T, XM_006722001.4:c.230G>A, XM_006722001.4:c.230G>C, XM_006722001.4:c.230G>T, XM_006722001.3:c.230G>A, XM_006722001.3:c.230G>C, XM_006722001.3:c.230G>T, XM_006722001.2:c.230G>A, XM_006722001.2:c.230G>C, XM_006722001.2:c.230G>T, XM_006722001.1:c.230G>A, XM_006722001.1:c.230G>C, XM_006722001.1:c.230G>T, XM_006722002.5:c.230G>A, XM_006722002.5:c.230G>C, XM_006722002.5:c.230G>T, XM_006722002.4:c.230G>A, XM_006722002.4:c.230G>C, XM_006722002.4:c.230G>T, XM_006722002.3:c.230G>A, XM_006722002.3:c.230G>C, XM_006722002.3:c.230G>T, XM_006722002.2:c.230G>A, XM_006722002.2:c.230G>C, XM_006722002.2:c.230G>T, XM_006722002.1:c.230G>A, XM_006722002.1:c.230G>C, XM_006722002.1:c.230G>T, XM_006722004.4:c.-122G>A, XM_006722004.4:c.-122G>C, XM_006722004.4:c.-122G>T, XM_006722004.3:c.-122G>A, XM_006722004.3:c.-122G>C, XM_006722004.3:c.-122G>T, XM_006722004.2:c.-122G>A, XM_006722004.2:c.-122G>C, XM_006722004.2:c.-122G>T, XM_006722004.1:c.-122G>A, XM_006722004.1:c.-122G>C, XM_006722004.1:c.-122G>T, XM_011525094.3:c.-122G>A, XM_011525094.3:c.-122G>C, XM_011525094.3:c.-122G>T, XM_011525094.2:c.-122G>A, XM_011525094.2:c.-122G>C, XM_011525094.2:c.-122G>T, XM_011525094.1:c.-122G>A, XM_011525094.1:c.-122G>C, XM_011525094.1:c.-122G>T, NM_058217.1:c.230G>A, NM_058217.1:c.230G>C, NM_058217.1:c.230G>T, XM_047436505.1:c.230G>A, XM_047436505.1:c.230G>C, XM_047436505.1:c.230G>T, NP_002867.1:p.Gly77Asp, NP_002867.1:p.Gly77Ala, NP_002867.1:p.Gly77Val, NP_478123.1:p.Gly77Asp, NP_478123.1:p.Gly77Ala, NP_478123.1:p.Gly77Val, XP_006722064.1:p.Gly77Asp, XP_006722064.1:p.Gly77Ala, XP_006722064.1:p.Gly77Val, XP_006722065.1:p.Gly77Asp, XP_006722065.1:p.Gly77Ala, XP_006722065.1:p.Gly77Val, XP_047292461.1:p.Gly77Asp, XP_047292461.1:p.Gly77Ala, XP_047292461.1:p.Gly77Val

                              15.

                              rs1444333199 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>A,G,T [Show Flanks]
                                Chromosome:
                                17:58720807 (GRCh38)
                                17:56798168 (GRCh37)
                                Canonical SPDI:
                                NC_000017.11:58720806:C:A,NC_000017.11:58720806:C:G,NC_000017.11:58720806:C:T
                                Gene:
                                RAD51C (Varview)
                                Functional Consequence:
                                missense_variant,genic_downstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant
                                Clinical significance:
                                uncertain-significance
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000017.11:g.58720807C>A, NC_000017.11:g.58720807C>G, NC_000017.11:g.58720807C>T, NC_000017.10:g.56798168C>A, NC_000017.10:g.56798168C>G, NC_000017.10:g.56798168C>T, NG_023199.1:g.33206C>A, NG_023199.1:g.33206C>G, NG_023199.1:g.33206C>T, NM_058216.3:c.899C>A, NM_058216.3:c.899C>G, NM_058216.3:c.899C>T, NM_058216.2:c.899C>A, NM_058216.2:c.899C>G, NM_058216.2:c.899C>T, NR_103872.2:n.774C>A, NR_103872.2:n.774C>G, NR_103872.2:n.774C>T, NR_103872.1:n.803C>A, NR_103872.1:n.803C>G, NR_103872.1:n.803C>T, XM_006722001.5:c.899C>A, XM_006722001.5:c.899C>G, XM_006722001.5:c.899C>T, XM_006722001.4:c.899C>A, XM_006722001.4:c.899C>G, XM_006722001.4:c.899C>T, XM_006722001.3:c.899C>A, XM_006722001.3:c.899C>G, XM_006722001.3:c.899C>T, XM_006722001.2:c.899C>A, XM_006722001.2:c.899C>G, XM_006722001.2:c.899C>T, XM_006722001.1:c.899C>A, XM_006722001.1:c.899C>G, XM_006722001.1:c.899C>T, XM_006722002.5:c.899C>A, XM_006722002.5:c.899C>G, XM_006722002.5:c.899C>T, XM_006722002.4:c.899C>A, XM_006722002.4:c.899C>G, XM_006722002.4:c.899C>T, XM_006722002.3:c.899C>A, XM_006722002.3:c.899C>G, XM_006722002.3:c.899C>T, XM_006722002.2:c.899C>A, XM_006722002.2:c.899C>G, XM_006722002.2:c.899C>T, XM_006722002.1:c.899C>A, XM_006722002.1:c.899C>G, XM_006722002.1:c.899C>T, XM_006722004.4:c.548C>A, XM_006722004.4:c.548C>G, XM_006722004.4:c.548C>T, XM_006722004.3:c.548C>A, XM_006722004.3:c.548C>G, XM_006722004.3:c.548C>T, XM_006722004.2:c.548C>A, XM_006722004.2:c.548C>G, XM_006722004.2:c.548C>T, XM_006722004.1:c.548C>A, XM_006722004.1:c.548C>G, XM_006722004.1:c.548C>T, XM_011525094.3:c.548C>A, XM_011525094.3:c.548C>G, XM_011525094.3:c.548C>T, XM_011525094.2:c.548C>A, XM_011525094.2:c.548C>G, XM_011525094.2:c.548C>T, XM_011525094.1:c.548C>A, XM_011525094.1:c.548C>G, XM_011525094.1:c.548C>T, NM_058217.1:c.*327C>A, NM_058217.1:c.*327C>G, NM_058217.1:c.*327C>T, NP_478123.1:p.Ala300Glu, NP_478123.1:p.Ala300Gly, NP_478123.1:p.Ala300Val, XP_006722064.1:p.Ala300Glu, XP_006722064.1:p.Ala300Gly, XP_006722064.1:p.Ala300Val, XP_006722065.1:p.Ala300Glu, XP_006722065.1:p.Ala300Gly, XP_006722065.1:p.Ala300Val, XP_006722067.1:p.Ala183Glu, XP_006722067.1:p.Ala183Gly, XP_006722067.1:p.Ala183Val, XP_011523396.1:p.Ala183Glu, XP_011523396.1:p.Ala183Gly, XP_011523396.1:p.Ala183Val

                                16.

                                rs1443654986 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>A,G,T [Show Flanks]
                                  Chromosome:
                                  17:58692664 (GRCh38)
                                  17:56770025 (GRCh37)
                                  Canonical SPDI:
                                  NC_000017.11:58692663:C:A,NC_000017.11:58692663:C:G,NC_000017.11:58692663:C:T
                                  Gene:
                                  RAD51C (Varview), TEX14 (Varview), IGBP1P2 (Varview)
                                  Functional Consequence:
                                  genic_upstream_transcript_variant,5_prime_UTR_variant,synonymous_variant,non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant
                                  Clinical significance:
                                  uncertain-significance,likely-benign
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000004/1 (TOPMED)
                                  G=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000017.11:g.58692664C>A, NC_000017.11:g.58692664C>G, NC_000017.11:g.58692664C>T, NC_000017.10:g.56770025C>A, NC_000017.10:g.56770025C>G, NC_000017.10:g.56770025C>T, NG_047169.1:g.4416G>T, NG_047169.1:g.4416G>C, NG_047169.1:g.4416G>A, NG_023199.1:g.5063C>A, NG_023199.1:g.5063C>G, NG_023199.1:g.5063C>T, NM_002876.4:c.21C>A, NM_002876.4:c.21C>G, NM_002876.4:c.21C>T, NM_002876.3:c.21C>A, NM_002876.3:c.21C>G, NM_002876.3:c.21C>T, NM_058216.3:c.21C>A, NM_058216.3:c.21C>G, NM_058216.3:c.21C>T, NM_058216.2:c.21C>A, NM_058216.2:c.21C>G, NM_058216.2:c.21C>T, NR_103872.2:n.63C>A, NR_103872.2:n.63C>G, NR_103872.2:n.63C>T, NR_103872.1:n.92C>A, NR_103872.1:n.92C>G, NR_103872.1:n.92C>T, NR_103873.1:n.92C>A, NR_103873.1:n.92C>G, NR_103873.1:n.92C>T, XM_006722001.5:c.21C>A, XM_006722001.5:c.21C>G, XM_006722001.5:c.21C>T, XM_006722001.4:c.21C>A, XM_006722001.4:c.21C>G, XM_006722001.4:c.21C>T, XM_006722001.3:c.21C>A, XM_006722001.3:c.21C>G, XM_006722001.3:c.21C>T, XM_006722001.2:c.21C>A, XM_006722001.2:c.21C>G, XM_006722001.2:c.21C>T, XM_006722001.1:c.21C>A, XM_006722001.1:c.21C>G, XM_006722001.1:c.21C>T, XM_006722002.5:c.21C>A, XM_006722002.5:c.21C>G, XM_006722002.5:c.21C>T, XM_006722002.4:c.21C>A, XM_006722002.4:c.21C>G, XM_006722002.4:c.21C>T, XM_006722002.3:c.21C>A, XM_006722002.3:c.21C>G, XM_006722002.3:c.21C>T, XM_006722002.2:c.21C>A, XM_006722002.2:c.21C>G, XM_006722002.2:c.21C>T, XM_006722002.1:c.21C>A, XM_006722002.1:c.21C>G, XM_006722002.1:c.21C>T, XM_006722004.4:c.-228C>A, XM_006722004.4:c.-228C>G, XM_006722004.4:c.-228C>T, XM_006722004.3:c.-228C>A, XM_006722004.3:c.-228C>G, XM_006722004.3:c.-228C>T, XM_006722004.2:c.-228C>A, XM_006722004.2:c.-228C>G, XM_006722004.2:c.-228C>T, XM_006722004.1:c.-228C>A, XM_006722004.1:c.-228C>G, XM_006722004.1:c.-228C>T, NM_058217.1:c.21C>A, NM_058217.1:c.21C>G, NM_058217.1:c.21C>T, XM_047436505.1:c.21C>A, XM_047436505.1:c.21C>G, XM_047436505.1:c.21C>T

                                  17.

                                  rs1442559963 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A,T [Show Flanks]
                                    Chromosome:
                                    17:58692770 (GRCh38)
                                    17:56770131 (GRCh37)
                                    Canonical SPDI:
                                    NC_000017.11:58692769:C:A,NC_000017.11:58692769:C:T
                                    Gene:
                                    RAD51C (Varview), TEX14 (Varview), IGBP1P2 (Varview)
                                    Functional Consequence:
                                    genic_upstream_transcript_variant,non_coding_transcript_variant,missense_variant,2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,intron_variant
                                    Clinical significance:
                                    uncertain-significance
                                    Validated:
                                    by frequency
                                    MAF:
                                    T=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000017.11:g.58692770C>A, NC_000017.11:g.58692770C>T, NC_000017.10:g.56770131C>A, NC_000017.10:g.56770131C>T, NG_047169.1:g.4310G>T, NG_047169.1:g.4310G>A, NG_023199.1:g.5169C>A, NG_023199.1:g.5169C>T, NM_002876.4:c.127C>A, NM_002876.4:c.127C>T, NM_002876.3:c.127C>A, NM_002876.3:c.127C>T, NM_058216.3:c.127C>A, NM_058216.3:c.127C>T, NM_058216.2:c.127C>A, NM_058216.2:c.127C>T, NR_103872.2:n.169C>A, NR_103872.2:n.169C>T, NR_103872.1:n.198C>A, NR_103872.1:n.198C>T, XM_006722001.5:c.127C>A, XM_006722001.5:c.127C>T, XM_006722001.4:c.127C>A, XM_006722001.4:c.127C>T, XM_006722001.3:c.127C>A, XM_006722001.3:c.127C>T, XM_006722001.2:c.127C>A, XM_006722001.2:c.127C>T, XM_006722001.1:c.127C>A, XM_006722001.1:c.127C>T, XM_006722002.5:c.127C>A, XM_006722002.5:c.127C>T, XM_006722002.4:c.127C>A, XM_006722002.4:c.127C>T, XM_006722002.3:c.127C>A, XM_006722002.3:c.127C>T, XM_006722002.2:c.127C>A, XM_006722002.2:c.127C>T, XM_006722002.1:c.127C>A, XM_006722002.1:c.127C>T, NM_058217.1:c.127C>A, NM_058217.1:c.127C>T, XM_047436505.1:c.127C>A, XM_047436505.1:c.127C>T, NP_002867.1:p.Pro43Thr, NP_002867.1:p.Pro43Ser, NP_478123.1:p.Pro43Thr, NP_478123.1:p.Pro43Ser, XP_006722064.1:p.Pro43Thr, XP_006722064.1:p.Pro43Ser, XP_006722065.1:p.Pro43Thr, XP_006722065.1:p.Pro43Ser, XP_047292461.1:p.Pro43Thr, XP_047292461.1:p.Pro43Ser

                                    18.

                                    rs1439877158 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      17:58720749 (GRCh38)
                                      17:56798110 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:58720748:A:G
                                      Gene:
                                      RAD51C (Varview)
                                      Functional Consequence:
                                      missense_variant,genic_downstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant
                                      Clinical significance:
                                      uncertain-significance
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0.000071/1 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1436204606 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        17:58732482 (GRCh38)
                                        17:56809843 (GRCh37)
                                        Canonical SPDI:
                                        NC_000017.11:58732481:A:G
                                        Gene:
                                        RAD51C (Varview), LOC105371843 (Varview)
                                        Functional Consequence:
                                        missense_variant,genic_downstream_transcript_variant,splice_acceptor_variant,coding_sequence_variant,intron_variant
                                        Clinical significance:
                                        uncertain-significance
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1435180142 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>A,C,G [Show Flanks]
                                          Chromosome:
                                          17:58696755 (GRCh38)
                                          17:56774116 (GRCh37)
                                          Canonical SPDI:
                                          NC_000017.11:58696754:T:A,NC_000017.11:58696754:T:C,NC_000017.11:58696754:T:G
                                          Gene:
                                          RAD51C (Varview)
                                          Functional Consequence:
                                          missense_variant,genic_downstream_transcript_variant,intron_variant,coding_sequence_variant
                                          Clinical significance:
                                          uncertain-significance
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0.000111/1 (ALFA)
                                          A=0.000004/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000017.11:g.58696755T>A, NC_000017.11:g.58696755T>C, NC_000017.11:g.58696755T>G, NC_000017.10:g.56774116T>A, NC_000017.10:g.56774116T>C, NC_000017.10:g.56774116T>G, NG_047169.1:g.325A>T, NG_047169.1:g.325A>G, NG_047169.1:g.325A>C, NG_023199.1:g.9154T>A, NG_023199.1:g.9154T>C, NG_023199.1:g.9154T>G, NM_058216.3:c.467T>A, NM_058216.3:c.467T>C, NM_058216.3:c.467T>G, NM_058216.2:c.467T>A, NM_058216.2:c.467T>C, NM_058216.2:c.467T>G, XM_006722001.5:c.467T>A, XM_006722001.5:c.467T>C, XM_006722001.5:c.467T>G, XM_006722001.4:c.467T>A, XM_006722001.4:c.467T>C, XM_006722001.4:c.467T>G, XM_006722001.3:c.467T>A, XM_006722001.3:c.467T>C, XM_006722001.3:c.467T>G, XM_006722001.2:c.467T>A, XM_006722001.2:c.467T>C, XM_006722001.2:c.467T>G, XM_006722001.1:c.467T>A, XM_006722001.1:c.467T>C, XM_006722001.1:c.467T>G, XM_006722002.5:c.467T>A, XM_006722002.5:c.467T>C, XM_006722002.5:c.467T>G, XM_006722002.4:c.467T>A, XM_006722002.4:c.467T>C, XM_006722002.4:c.467T>G, XM_006722002.3:c.467T>A, XM_006722002.3:c.467T>C, XM_006722002.3:c.467T>G, XM_006722002.2:c.467T>A, XM_006722002.2:c.467T>C, XM_006722002.2:c.467T>G, XM_006722002.1:c.467T>A, XM_006722002.1:c.467T>C, XM_006722002.1:c.467T>G, XM_006722004.4:c.116T>A, XM_006722004.4:c.116T>C, XM_006722004.4:c.116T>G, XM_006722004.3:c.116T>A, XM_006722004.3:c.116T>C, XM_006722004.3:c.116T>G, XM_006722004.2:c.116T>A, XM_006722004.2:c.116T>C, XM_006722004.2:c.116T>G, XM_006722004.1:c.116T>A, XM_006722004.1:c.116T>C, XM_006722004.1:c.116T>G, XM_011525094.3:c.116T>A, XM_011525094.3:c.116T>C, XM_011525094.3:c.116T>G, XM_011525094.2:c.116T>A, XM_011525094.2:c.116T>C, XM_011525094.2:c.116T>G, XM_011525094.1:c.116T>A, XM_011525094.1:c.116T>C, XM_011525094.1:c.116T>G, XM_047436505.1:c.467T>A, XM_047436505.1:c.467T>C, XM_047436505.1:c.467T>G, NP_478123.1:p.Val156Asp, NP_478123.1:p.Val156Ala, NP_478123.1:p.Val156Gly, XP_006722064.1:p.Val156Asp, XP_006722064.1:p.Val156Ala, XP_006722064.1:p.Val156Gly, XP_006722065.1:p.Val156Asp, XP_006722065.1:p.Val156Ala, XP_006722065.1:p.Val156Gly, XP_006722067.1:p.Val39Asp, XP_006722067.1:p.Val39Ala, XP_006722067.1:p.Val39Gly, XP_011523396.1:p.Val39Asp, XP_011523396.1:p.Val39Ala, XP_011523396.1:p.Val39Gly, XP_047292461.1:p.Val156Asp, XP_047292461.1:p.Val156Ala, XP_047292461.1:p.Val156Gly

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