U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 11118

1.

rs1491549583 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    CA>- [Show Flanks]
    Chromosome:
    15:40729372 (GRCh38)
    15:41021570 (GRCh37)
    Canonical SPDI:
    NC_000015.10:40729371:CA:
    Gene:
    RAD51 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    -=0.00194/23 (ALFA)
    -=0.00221/62 (TOMMO)
    HGVS:

    2.

    rs1491504110 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->ATTT [Show Flanks]
      Chromosome:
      15:40693737 (GRCh38)
      15:40985936 (GRCh37)
      Canonical SPDI:
      NC_000015.10:40693737:TTT:TTTATTT
      Gene:
      RAD51 (Varview), RAD51-AS1 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      TTTATTT=0./0 (ALFA)
      TTTA=0.000004/1 (TOPMED)
      HGVS:

      3.

      rs1491494057 has merged into rs398039433 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TTTTTTTTTTTTTTTT>-,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        15:40712881 (GRCh38)
        15:41005079 (GRCh37)
        Canonical SPDI:
        NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40712877:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        RAD51 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTT=0./0 (ALFA)
        HGVS:
        NC_000015.10:g.40712881_40712896del, NC_000015.10:g.40712887_40712896del, NC_000015.10:g.40712888_40712896del, NC_000015.10:g.40712889_40712896del, NC_000015.10:g.40712890_40712896del, NC_000015.10:g.40712892_40712896del, NC_000015.10:g.40712893_40712896del, NC_000015.10:g.40712894_40712896del, NC_000015.10:g.40712895_40712896del, NC_000015.10:g.40712896del, NC_000015.10:g.40712896dup, NC_000015.10:g.40712895_40712896dup, NC_000015.10:g.40712894_40712896dup, NC_000015.10:g.40712893_40712896dup, NC_000015.10:g.40712892_40712896dup, NC_000015.10:g.40712891_40712896dup, NC_000015.10:g.40712890_40712896dup, NC_000015.10:g.40712889_40712896dup, NC_000015.10:g.40712888_40712896dup, NC_000015.10:g.40712887_40712896dup, NC_000015.10:g.40712886_40712896dup, NC_000015.10:g.40712885_40712896dup, NC_000015.10:g.40712884_40712896dup, NC_000015.10:g.40712883_40712896dup, NC_000015.10:g.40712882_40712896dup, NC_000015.10:g.40712881_40712896dup, NC_000015.9:g.41005079_41005094del, NC_000015.9:g.41005085_41005094del, NC_000015.9:g.41005086_41005094del, NC_000015.9:g.41005087_41005094del, NC_000015.9:g.41005088_41005094del, NC_000015.9:g.41005090_41005094del, NC_000015.9:g.41005091_41005094del, NC_000015.9:g.41005092_41005094del, NC_000015.9:g.41005093_41005094del, NC_000015.9:g.41005094del, NC_000015.9:g.41005094dup, NC_000015.9:g.41005093_41005094dup, NC_000015.9:g.41005092_41005094dup, NC_000015.9:g.41005091_41005094dup, NC_000015.9:g.41005090_41005094dup, NC_000015.9:g.41005089_41005094dup, NC_000015.9:g.41005088_41005094dup, NC_000015.9:g.41005087_41005094dup, NC_000015.9:g.41005086_41005094dup, NC_000015.9:g.41005085_41005094dup, NC_000015.9:g.41005084_41005094dup, NC_000015.9:g.41005083_41005094dup, NC_000015.9:g.41005082_41005094dup, NC_000015.9:g.41005081_41005094dup, NC_000015.9:g.41005080_41005094dup, NC_000015.9:g.41005079_41005094dup, NG_012120.1:g.22721_22736del, NG_012120.1:g.22727_22736del, NG_012120.1:g.22728_22736del, NG_012120.1:g.22729_22736del, NG_012120.1:g.22730_22736del, NG_012120.1:g.22732_22736del, NG_012120.1:g.22733_22736del, NG_012120.1:g.22734_22736del, NG_012120.1:g.22735_22736del, NG_012120.1:g.22736del, NG_012120.1:g.22736dup, NG_012120.1:g.22735_22736dup, NG_012120.1:g.22734_22736dup, NG_012120.1:g.22733_22736dup, NG_012120.1:g.22732_22736dup, NG_012120.1:g.22731_22736dup, NG_012120.1:g.22730_22736dup, NG_012120.1:g.22729_22736dup, NG_012120.1:g.22728_22736dup, NG_012120.1:g.22727_22736dup, NG_012120.1:g.22726_22736dup, NG_012120.1:g.22725_22736dup, NG_012120.1:g.22724_22736dup, NG_012120.1:g.22723_22736dup, NG_012120.1:g.22722_22736dup, NG_012120.1:g.22721_22736dup

        4.

        rs1491489886 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->GAG [Show Flanks]
          Chromosome:
          15:40707741 (GRCh38)
          15:40999940 (GRCh37)
          Canonical SPDI:
          NC_000015.10:40707741:GAG:GAGGAG
          Gene:
          RAD51 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by cluster
          HGVS:

          5.

          rs1491476452 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->C [Show Flanks]
            Chromosome:
            15:40713995 (GRCh38)
            15:41006194 (GRCh37)
            Canonical SPDI:
            NC_000015.10:40713995::C
            Gene:
            RAD51 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            C=0./0 (ALFA)
            C=0.00021/4 (GnomAD)
            HGVS:

            6.

            rs1491453349 has merged into rs778467789 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTTTTTT>-,T,TTT,TTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              15:40730527 (GRCh38)
              15:41022725 (GRCh37)
              Canonical SPDI:
              NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              RAD51 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTT=0./0 (ALFA)
              -=0.05/2 (GENOME_DK)
              HGVS:
              NC_000015.10:g.40730527_40730539del, NC_000015.10:g.40730528_40730539del, NC_000015.10:g.40730530_40730539del, NC_000015.10:g.40730531_40730539del, NC_000015.10:g.40730534_40730539del, NC_000015.10:g.40730535_40730539del, NC_000015.10:g.40730536_40730539del, NC_000015.10:g.40730537_40730539del, NC_000015.10:g.40730538_40730539del, NC_000015.10:g.40730539del, NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.10:g.40730539dup, NC_000015.10:g.40730538_40730539dup, NC_000015.10:g.40730537_40730539dup, NC_000015.10:g.40730536_40730539dup, NC_000015.10:g.40730535_40730539dup, NC_000015.10:g.40730534_40730539dup, NC_000015.10:g.40730533_40730539dup, NC_000015.10:g.40730532_40730539dup, NC_000015.10:g.40730522_40730539dup, NC_000015.10:g.40730521_40730539dup, NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41022725_41022737del, NC_000015.9:g.41022726_41022737del, NC_000015.9:g.41022728_41022737del, NC_000015.9:g.41022729_41022737del, NC_000015.9:g.41022732_41022737del, NC_000015.9:g.41022733_41022737del, NC_000015.9:g.41022734_41022737del, NC_000015.9:g.41022735_41022737del, NC_000015.9:g.41022736_41022737del, NC_000015.9:g.41022737del, NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.9:g.41022737dup, NC_000015.9:g.41022736_41022737dup, NC_000015.9:g.41022735_41022737dup, NC_000015.9:g.41022734_41022737dup, NC_000015.9:g.41022733_41022737dup, NC_000015.9:g.41022732_41022737dup, NC_000015.9:g.41022731_41022737dup, NC_000015.9:g.41022730_41022737dup, NC_000015.9:g.41022720_41022737dup, NC_000015.9:g.41022719_41022737dup, NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTTT, NG_012120.1:g.40367_40379del, NG_012120.1:g.40368_40379del, NG_012120.1:g.40370_40379del, NG_012120.1:g.40371_40379del, NG_012120.1:g.40374_40379del, NG_012120.1:g.40375_40379del, NG_012120.1:g.40376_40379del, NG_012120.1:g.40377_40379del, NG_012120.1:g.40378_40379del, NG_012120.1:g.40379del, NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_012120.1:g.40379dup, NG_012120.1:g.40378_40379dup, NG_012120.1:g.40377_40379dup, NG_012120.1:g.40376_40379dup, NG_012120.1:g.40375_40379dup, NG_012120.1:g.40374_40379dup, NG_012120.1:g.40373_40379dup, NG_012120.1:g.40372_40379dup, NG_012120.1:g.40362_40379dup, NG_012120.1:g.40361_40379dup, NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTT, NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTT, NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTTT

              7.

              rs1491450663 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->TTTTTTTTTTTTTTCTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                15:40727861 (GRCh38)
                15:41020060 (GRCh37)
                Canonical SPDI:
                NC_000015.10:40727861:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTT
                Gene:
                RAD51 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTT=0.0002/1 (ALFA)
                HGVS:

                8.

                rs1491430082 [Homo sapiens]
                  Variant type:
                  INS
                  Alleles:
                  ->G [Show Flanks]
                  Chromosome:
                  15:40726913 (GRCh38)
                  15:41019112 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:40726913::G
                  Gene:
                  RAD51 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0.01189/141 (ALFA)
                  G=0.06209/2036 (GnomAD)
                  HGVS:

                  9.

                  rs1491386958 has merged into rs71104728 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    15:40710252 (GRCh38)
                    15:41002450 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40710241:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    RAD51 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAA=0./0 (ALFA)
                    HGVS:
                    NC_000015.10:g.40710252_40710270del, NC_000015.10:g.40710253_40710270del, NC_000015.10:g.40710254_40710270del, NC_000015.10:g.40710255_40710270del, NC_000015.10:g.40710256_40710270del, NC_000015.10:g.40710257_40710270del, NC_000015.10:g.40710258_40710270del, NC_000015.10:g.40710259_40710270del, NC_000015.10:g.40710260_40710270del, NC_000015.10:g.40710261_40710270del, NC_000015.10:g.40710262_40710270del, NC_000015.10:g.40710263_40710270del, NC_000015.10:g.40710264_40710270del, NC_000015.10:g.40710265_40710270del, NC_000015.10:g.40710266_40710270del, NC_000015.10:g.40710267_40710270del, NC_000015.10:g.40710268_40710270del, NC_000015.10:g.40710269_40710270del, NC_000015.10:g.40710270del, NC_000015.10:g.40710270dup, NC_000015.10:g.40710269_40710270dup, NC_000015.10:g.40710268_40710270dup, NC_000015.10:g.40710267_40710270dup, NC_000015.10:g.40710266_40710270dup, NC_000015.10:g.40710265_40710270dup, NC_000015.10:g.40710264_40710270dup, NC_000015.10:g.40710263_40710270dup, NC_000015.10:g.40710262_40710270dup, NC_000015.10:g.40710255_40710270dup, NC_000015.10:g.40710254_40710270dup, NC_000015.10:g.40710253_40710270dup, NC_000015.10:g.40710252_40710270dup, NC_000015.10:g.40710249_40710270dup, NC_000015.10:g.40710243_40710270dup, NC_000015.9:g.41002450_41002468del, NC_000015.9:g.41002451_41002468del, NC_000015.9:g.41002452_41002468del, NC_000015.9:g.41002453_41002468del, NC_000015.9:g.41002454_41002468del, NC_000015.9:g.41002455_41002468del, NC_000015.9:g.41002456_41002468del, NC_000015.9:g.41002457_41002468del, NC_000015.9:g.41002458_41002468del, NC_000015.9:g.41002459_41002468del, NC_000015.9:g.41002460_41002468del, NC_000015.9:g.41002461_41002468del, NC_000015.9:g.41002462_41002468del, NC_000015.9:g.41002463_41002468del, NC_000015.9:g.41002464_41002468del, NC_000015.9:g.41002465_41002468del, NC_000015.9:g.41002466_41002468del, NC_000015.9:g.41002467_41002468del, NC_000015.9:g.41002468del, NC_000015.9:g.41002468dup, NC_000015.9:g.41002467_41002468dup, NC_000015.9:g.41002466_41002468dup, NC_000015.9:g.41002465_41002468dup, NC_000015.9:g.41002464_41002468dup, NC_000015.9:g.41002463_41002468dup, NC_000015.9:g.41002462_41002468dup, NC_000015.9:g.41002461_41002468dup, NC_000015.9:g.41002460_41002468dup, NC_000015.9:g.41002453_41002468dup, NC_000015.9:g.41002452_41002468dup, NC_000015.9:g.41002451_41002468dup, NC_000015.9:g.41002450_41002468dup, NC_000015.9:g.41002447_41002468dup, NC_000015.9:g.41002441_41002468dup, NG_012120.1:g.20092_20110del, NG_012120.1:g.20093_20110del, NG_012120.1:g.20094_20110del, NG_012120.1:g.20095_20110del, NG_012120.1:g.20096_20110del, NG_012120.1:g.20097_20110del, NG_012120.1:g.20098_20110del, NG_012120.1:g.20099_20110del, NG_012120.1:g.20100_20110del, NG_012120.1:g.20101_20110del, NG_012120.1:g.20102_20110del, NG_012120.1:g.20103_20110del, NG_012120.1:g.20104_20110del, NG_012120.1:g.20105_20110del, NG_012120.1:g.20106_20110del, NG_012120.1:g.20107_20110del, NG_012120.1:g.20108_20110del, NG_012120.1:g.20109_20110del, NG_012120.1:g.20110del, NG_012120.1:g.20110dup, NG_012120.1:g.20109_20110dup, NG_012120.1:g.20108_20110dup, NG_012120.1:g.20107_20110dup, NG_012120.1:g.20106_20110dup, NG_012120.1:g.20105_20110dup, NG_012120.1:g.20104_20110dup, NG_012120.1:g.20103_20110dup, NG_012120.1:g.20102_20110dup, NG_012120.1:g.20095_20110dup, NG_012120.1:g.20094_20110dup, NG_012120.1:g.20093_20110dup, NG_012120.1:g.20092_20110dup, NG_012120.1:g.20089_20110dup, NG_012120.1:g.20083_20110dup

                    10.

                    rs1491364832 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      CT>- [Show Flanks]
                      Chromosome:
                      15:40724674 (GRCh38)
                      15:41016872 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:40724672:TCT:T
                      Gene:
                      RAD51 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      T=0.00017/2 (ALFA)
                      -=0.00057/57 (GnomAD)
                      HGVS:

                      11.

                      rs1491344989 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->A [Show Flanks]
                        Chromosome:
                        15:40713262 (GRCh38)
                        15:41005461 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:40713262:A:AA
                        Gene:
                        RAD51 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        AA=0./0 (ALFA)
                        A=0.000015/2 (GnomAD)
                        HGVS:

                        12.

                        rs1491341255 has merged into rs11315096 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          TTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
                          Chromosome:
                          15:40693749 (GRCh38)
                          15:40985947 (GRCh37)
                          Canonical SPDI:
                          NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40693736:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
                          Gene:
                          RAD51 (Varview), RAD51-AS1 (Varview)
                          Functional Consequence:
                          upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          TTTTTTTTTTTTTTT=0./0 (ALFA)
                          T=0.0291/108 (TWINSUK)
                          T=0.034/131 (ALSPAC)
                          T=0.3/12 (GENOME_DK)
                          -=0.3729/223 (NorthernSweden)
                          HGVS:
                          NC_000015.10:g.40693749_40693756del, NC_000015.10:g.40693751_40693756del, NC_000015.10:g.40693752_40693756del, NC_000015.10:g.40693753_40693756del, NC_000015.10:g.40693754_40693756del, NC_000015.10:g.40693755_40693756del, NC_000015.10:g.40693756del, NC_000015.10:g.40693756dup, NC_000015.10:g.40693755_40693756dup, NC_000015.10:g.40693749_40693756dup, NC_000015.9:g.40985947_40985954del, NC_000015.9:g.40985949_40985954del, NC_000015.9:g.40985950_40985954del, NC_000015.9:g.40985951_40985954del, NC_000015.9:g.40985952_40985954del, NC_000015.9:g.40985953_40985954del, NC_000015.9:g.40985954del, NC_000015.9:g.40985954dup, NC_000015.9:g.40985953_40985954dup, NC_000015.9:g.40985947_40985954dup, NG_012120.1:g.3589_3596del, NG_012120.1:g.3591_3596del, NG_012120.1:g.3592_3596del, NG_012120.1:g.3593_3596del, NG_012120.1:g.3594_3596del, NG_012120.1:g.3595_3596del, NG_012120.1:g.3596del, NG_012120.1:g.3596dup, NG_012120.1:g.3595_3596dup, NG_012120.1:g.3589_3596dup, NR_040058.1:n.1146_1153del, NR_040058.1:n.1148_1153del, NR_040058.1:n.1149_1153del, NR_040058.1:n.1150_1153del, NR_040058.1:n.1151_1153del, NR_040058.1:n.1152_1153del, NR_040058.1:n.1153del, NR_040058.1:n.1153dup, NR_040058.1:n.1152_1153dup, NR_040058.1:n.1146_1153dup

                          13.

                          rs1491306177 [Homo sapiens]
                            Variant type:
                            INS
                            Alleles:
                            ->G [Show Flanks]
                            Chromosome:
                            15:40719832 (GRCh38)
                            15:41012031 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:40719832::G
                            Gene:
                            RAD51 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000011/3 (TOPMED)
                            G=0.000026/1 (GnomAD)
                            HGVS:

                            14.

                            rs1491251953 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              AT>-,ATAT [Show Flanks]
                              Chromosome:
                              15:40713263 (GRCh38)
                              15:41005461 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:40713261:TAT:T,NC_000015.10:40713261:TAT:TATAT
                              Gene:
                              RAD51 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TATAT=0./0 (ALFA)
                              HGVS:

                              15.

                              rs1491244772 has merged into rs754071390 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
                                Chromosome:
                                15:40727872 (GRCh38)
                                15:41020070 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40727860:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
                                Gene:
                                RAD51 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TTTTTTTTTTTTTT=0./0 (ALFA)
                                T=0.375/15 (GENOME_DK)
                                HGVS:
                                NC_000015.10:g.40727872_40727877del, NC_000015.10:g.40727874_40727877del, NC_000015.10:g.40727875_40727877del, NC_000015.10:g.40727876_40727877del, NC_000015.10:g.40727877del, NC_000015.10:g.40727877dup, NC_000015.10:g.40727876_40727877dup, NC_000015.10:g.40727875_40727877dup, NC_000015.10:g.40727874_40727877dup, NC_000015.10:g.40727871_40727877dup, NC_000015.9:g.41020070_41020075del, NC_000015.9:g.41020072_41020075del, NC_000015.9:g.41020073_41020075del, NC_000015.9:g.41020074_41020075del, NC_000015.9:g.41020075del, NC_000015.9:g.41020075dup, NC_000015.9:g.41020074_41020075dup, NC_000015.9:g.41020073_41020075dup, NC_000015.9:g.41020072_41020075dup, NC_000015.9:g.41020069_41020075dup, NG_012120.1:g.37712_37717del, NG_012120.1:g.37714_37717del, NG_012120.1:g.37715_37717del, NG_012120.1:g.37716_37717del, NG_012120.1:g.37717del, NG_012120.1:g.37717dup, NG_012120.1:g.37716_37717dup, NG_012120.1:g.37715_37717dup, NG_012120.1:g.37714_37717dup, NG_012120.1:g.37711_37717dup

                                16.

                                rs1491233213 has merged into rs60375696 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                                  Chromosome:
                                  15:40729385 (GRCh38)
                                  15:41021583 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:40729372:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                                  Gene:
                                  RAD51 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AAAAAAAAAAAA=0./0 (ALFA)
                                  -=0.000008/2 (TOPMED)
                                  -=0.497604/2492 (1000Genomes)
                                  HGVS:
                                  NC_000015.10:g.40729385_40729397del, NC_000015.10:g.40729386_40729397del, NC_000015.10:g.40729387_40729397del, NC_000015.10:g.40729388_40729397del, NC_000015.10:g.40729389_40729397del, NC_000015.10:g.40729390_40729397del, NC_000015.10:g.40729391_40729397del, NC_000015.10:g.40729392_40729397del, NC_000015.10:g.40729393_40729397del, NC_000015.10:g.40729394_40729397del, NC_000015.10:g.40729395_40729397del, NC_000015.10:g.40729396_40729397del, NC_000015.10:g.40729397del, NC_000015.10:g.40729397dup, NC_000015.10:g.40729396_40729397dup, NC_000015.10:g.40729395_40729397dup, NC_000015.10:g.40729394_40729397dup, NC_000015.10:g.40729393_40729397dup, NC_000015.10:g.40729392_40729397dup, NC_000015.10:g.40729391_40729397dup, NC_000015.10:g.40729390_40729397dup, NC_000015.10:g.40729386_40729397dup, NC_000015.10:g.40729378_40729397dup, NC_000015.10:g.40729377_40729397dup, NC_000015.10:g.40729397_40729398insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.41021583_41021595del, NC_000015.9:g.41021584_41021595del, NC_000015.9:g.41021585_41021595del, NC_000015.9:g.41021586_41021595del, NC_000015.9:g.41021587_41021595del, NC_000015.9:g.41021588_41021595del, NC_000015.9:g.41021589_41021595del, NC_000015.9:g.41021590_41021595del, NC_000015.9:g.41021591_41021595del, NC_000015.9:g.41021592_41021595del, NC_000015.9:g.41021593_41021595del, NC_000015.9:g.41021594_41021595del, NC_000015.9:g.41021595del, NC_000015.9:g.41021595dup, NC_000015.9:g.41021594_41021595dup, NC_000015.9:g.41021593_41021595dup, NC_000015.9:g.41021592_41021595dup, NC_000015.9:g.41021591_41021595dup, NC_000015.9:g.41021590_41021595dup, NC_000015.9:g.41021589_41021595dup, NC_000015.9:g.41021588_41021595dup, NC_000015.9:g.41021584_41021595dup, NC_000015.9:g.41021576_41021595dup, NC_000015.9:g.41021575_41021595dup, NC_000015.9:g.41021595_41021596insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012120.1:g.39225_39237del, NG_012120.1:g.39226_39237del, NG_012120.1:g.39227_39237del, NG_012120.1:g.39228_39237del, NG_012120.1:g.39229_39237del, NG_012120.1:g.39230_39237del, NG_012120.1:g.39231_39237del, NG_012120.1:g.39232_39237del, NG_012120.1:g.39233_39237del, NG_012120.1:g.39234_39237del, NG_012120.1:g.39235_39237del, NG_012120.1:g.39236_39237del, NG_012120.1:g.39237del, NG_012120.1:g.39237dup, NG_012120.1:g.39236_39237dup, NG_012120.1:g.39235_39237dup, NG_012120.1:g.39234_39237dup, NG_012120.1:g.39233_39237dup, NG_012120.1:g.39232_39237dup, NG_012120.1:g.39231_39237dup, NG_012120.1:g.39230_39237dup, NG_012120.1:g.39226_39237dup, NG_012120.1:g.39218_39237dup, NG_012120.1:g.39217_39237dup, NG_012120.1:g.39237_39238insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                                  17.

                                  rs1491223280 has merged into rs749995356 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    TTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                    Chromosome:
                                    15:40714006 (GRCh38)
                                    15:41006204 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:40713994:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                    Gene:
                                    RAD51 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    TTTTTTTTTTTTTTT=0./0 (ALFA)
                                    HGVS:
                                    NC_000015.10:g.40714006_40714012del, NC_000015.10:g.40714009_40714012del, NC_000015.10:g.40714010_40714012del, NC_000015.10:g.40714011_40714012del, NC_000015.10:g.40714012del, NC_000015.10:g.40714012dup, NC_000015.10:g.40714011_40714012dup, NC_000015.10:g.40714010_40714012dup, NC_000015.10:g.40714009_40714012dup, NC_000015.10:g.40714008_40714012dup, NC_000015.10:g.40714007_40714012dup, NC_000015.10:g.40714006_40714012dup, NC_000015.10:g.40714005_40714012dup, NC_000015.10:g.40714004_40714012dup, NC_000015.10:g.40714003_40714012dup, NC_000015.10:g.40714002_40714012dup, NC_000015.10:g.40714001_40714012dup, NC_000015.10:g.40714000_40714012dup, NC_000015.10:g.40713999_40714012dup, NC_000015.10:g.40714012_40714013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.40714012_40714013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41006204_41006210del, NC_000015.9:g.41006207_41006210del, NC_000015.9:g.41006208_41006210del, NC_000015.9:g.41006209_41006210del, NC_000015.9:g.41006210del, NC_000015.9:g.41006210dup, NC_000015.9:g.41006209_41006210dup, NC_000015.9:g.41006208_41006210dup, NC_000015.9:g.41006207_41006210dup, NC_000015.9:g.41006206_41006210dup, NC_000015.9:g.41006205_41006210dup, NC_000015.9:g.41006204_41006210dup, NC_000015.9:g.41006203_41006210dup, NC_000015.9:g.41006202_41006210dup, NC_000015.9:g.41006201_41006210dup, NC_000015.9:g.41006200_41006210dup, NC_000015.9:g.41006199_41006210dup, NC_000015.9:g.41006198_41006210dup, NC_000015.9:g.41006197_41006210dup, NC_000015.9:g.41006210_41006211insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41006210_41006211insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_012120.1:g.23846_23852del, NG_012120.1:g.23849_23852del, NG_012120.1:g.23850_23852del, NG_012120.1:g.23851_23852del, NG_012120.1:g.23852del, NG_012120.1:g.23852dup, NG_012120.1:g.23851_23852dup, NG_012120.1:g.23850_23852dup, NG_012120.1:g.23849_23852dup, NG_012120.1:g.23848_23852dup, NG_012120.1:g.23847_23852dup, NG_012120.1:g.23846_23852dup, NG_012120.1:g.23845_23852dup, NG_012120.1:g.23844_23852dup, NG_012120.1:g.23843_23852dup, NG_012120.1:g.23842_23852dup, NG_012120.1:g.23841_23852dup, NG_012120.1:g.23840_23852dup, NG_012120.1:g.23839_23852dup, NG_012120.1:g.23852_23853insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_012120.1:g.23852_23853insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                                    18.

                                    rs1491211599 [Homo sapiens]
                                      Variant type:
                                      DEL
                                      Alleles:
                                      GA>- [Show Flanks]
                                      Chromosome:
                                      15:40710537 (GRCh38)
                                      15:41002735 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:40710536:GA:
                                      Gene:
                                      RAD51 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      -=0./0 (ALFA)
                                      -=0.000023/3 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1491202397 [Homo sapiens]
                                        Variant type:
                                        DEL
                                        Alleles:
                                        TA>- [Show Flanks]
                                        Chromosome:
                                        15:40691377 (GRCh38)
                                        15:40983575 (GRCh37)
                                        Canonical SPDI:
                                        NC_000015.10:40691376:TA:
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        -=0./0 (ALFA)
                                        -=0.000024/3 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1491197896 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          CA>- [Show Flanks]
                                          Chromosome:
                                          15:40710241 (GRCh38)
                                          15:41002439 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:40710240:CA:
                                          Gene:
                                          RAD51 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          -=0./0 (ALFA)
                                          -=0.00146/18 (TOMMO)
                                          HGVS:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity