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Items: 1 to 20 of 10708

1.

rs1491541162 has merged into rs796099348 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    GGGGG>-,GG,GGG,GGGG,GGGGGG,GGGGGGG,GGGGGGGG,GGGGGGGGG,GGGGGGGGGG,GGGGGGGGGGG,GGGGGGGGGGGG,GGGGGGGGGGGGGG [Show Flanks]
    Chromosome:
    17:58692133 (GRCh38)
    17:56769494 (GRCh37)
    Canonical SPDI:
    NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG,NC_000017.11:58692125:GGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG
    Gene:
    RAD51C (Varview), TEX14 (Varview), IGBP1P2 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    GGGGGGGGG=0./0 (ALFA)
    HGVS:
    NC_000017.11:g.58692133_58692137del, NC_000017.11:g.58692135_58692137del, NC_000017.11:g.58692136_58692137del, NC_000017.11:g.58692137del, NC_000017.11:g.58692137dup, NC_000017.11:g.58692136_58692137dup, NC_000017.11:g.58692135_58692137dup, NC_000017.11:g.58692134_58692137dup, NC_000017.11:g.58692133_58692137dup, NC_000017.11:g.58692132_58692137dup, NC_000017.11:g.58692131_58692137dup, NC_000017.11:g.58692129_58692137dup, NC_000017.10:g.56769494_56769498del, NC_000017.10:g.56769496_56769498del, NC_000017.10:g.56769497_56769498del, NC_000017.10:g.56769498del, NC_000017.10:g.56769498dup, NC_000017.10:g.56769497_56769498dup, NC_000017.10:g.56769496_56769498dup, NC_000017.10:g.56769495_56769498dup, NC_000017.10:g.56769494_56769498dup, NC_000017.10:g.56769493_56769498dup, NC_000017.10:g.56769492_56769498dup, NC_000017.10:g.56769490_56769498dup, NG_047169.1:g.4950_4954del, NG_047169.1:g.4952_4954del, NG_047169.1:g.4953_4954del, NG_047169.1:g.4954del, NG_047169.1:g.4954dup, NG_047169.1:g.4953_4954dup, NG_047169.1:g.4952_4954dup, NG_047169.1:g.4951_4954dup, NG_047169.1:g.4950_4954dup, NG_047169.1:g.4949_4954dup, NG_047169.1:g.4948_4954dup, NG_047169.1:g.4946_4954dup, NG_023199.1:g.4532_4536del, NG_023199.1:g.4534_4536del, NG_023199.1:g.4535_4536del, NG_023199.1:g.4536del, NG_023199.1:g.4536dup, NG_023199.1:g.4535_4536dup, NG_023199.1:g.4534_4536dup, NG_023199.1:g.4533_4536dup, NG_023199.1:g.4532_4536dup, NG_023199.1:g.4531_4536dup, NG_023199.1:g.4530_4536dup, NG_023199.1:g.4528_4536dup

    2.

    rs1491456229 has merged into rs77247264 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      17:58731272 (GRCh38)
      17:56808633 (GRCh37)
      Canonical SPDI:
      NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58731258:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      RAD51C (Varview), LOC105371843 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTTTTTTTTTT=0./0 (ALFA)
      T=0.085/51 (NorthernSweden)
      T=0.17452/874 (1000Genomes)
      T=0.375/15 (GENOME_DK)
      -=0.5/4 (KOREAN)
      HGVS:
      NC_000017.11:g.58731272_58731275del, NC_000017.11:g.58731273_58731275del, NC_000017.11:g.58731274_58731275del, NC_000017.11:g.58731275del, NC_000017.11:g.58731275dup, NC_000017.11:g.58731274_58731275dup, NC_000017.11:g.58731273_58731275dup, NC_000017.11:g.58731272_58731275dup, NC_000017.11:g.58731270_58731275dup, NC_000017.11:g.58731266_58731275dup, NC_000017.11:g.58731275_58731276insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000017.10:g.56808633_56808636del, NC_000017.10:g.56808634_56808636del, NC_000017.10:g.56808635_56808636del, NC_000017.10:g.56808636del, NC_000017.10:g.56808636dup, NC_000017.10:g.56808635_56808636dup, NC_000017.10:g.56808634_56808636dup, NC_000017.10:g.56808633_56808636dup, NC_000017.10:g.56808631_56808636dup, NC_000017.10:g.56808627_56808636dup, NC_000017.10:g.56808636_56808637insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023199.1:g.43671_43674del, NG_023199.1:g.43672_43674del, NG_023199.1:g.43673_43674del, NG_023199.1:g.43674del, NG_023199.1:g.43674dup, NG_023199.1:g.43673_43674dup, NG_023199.1:g.43672_43674dup, NG_023199.1:g.43671_43674dup, NG_023199.1:g.43669_43674dup, NG_023199.1:g.43665_43674dup, NG_023199.1:g.43674_43675insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

      3.

      rs1491400013 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CA>- [Show Flanks]
        Chromosome:
        17:58712344 (GRCh38)
        17:56789705 (GRCh37)
        Canonical SPDI:
        NC_000017.11:58712343:CA:
        Gene:
        RAD51C (Varview)
        Functional Consequence:
        genic_downstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0.00809/96 (ALFA)
        HGVS:

        4.

        rs1491382782 has merged into rs34570887 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          TTTTTTTTTTTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
          Chromosome:
          17:58709101 (GRCh38)
          17:56786462 (GRCh37)
          Canonical SPDI:
          NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:58709092:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
          Gene:
          RAD51C (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TTTTTTTT=0./0 (ALFA)
          -=0.4553/2280 (1000Genomes)
          HGVS:
          NC_000017.11:g.58709101_58709112del, NC_000017.11:g.58709102_58709112del, NC_000017.11:g.58709103_58709112del, NC_000017.11:g.58709105_58709112del, NC_000017.11:g.58709106_58709112del, NC_000017.11:g.58709107_58709112del, NC_000017.11:g.58709108_58709112del, NC_000017.11:g.58709109_58709112del, NC_000017.11:g.58709110_58709112del, NC_000017.11:g.58709111_58709112del, NC_000017.11:g.58709112del, NC_000017.11:g.58709112dup, NC_000017.11:g.58709111_58709112dup, NC_000017.11:g.58709110_58709112dup, NC_000017.11:g.58709109_58709112dup, NC_000017.11:g.58709108_58709112dup, NC_000017.11:g.58709093_58709112T[26]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000017.11:g.58709095_58709112dup, NC_000017.11:g.58709094_58709112dup, NC_000017.10:g.56786462_56786473del, NC_000017.10:g.56786463_56786473del, NC_000017.10:g.56786464_56786473del, NC_000017.10:g.56786466_56786473del, NC_000017.10:g.56786467_56786473del, NC_000017.10:g.56786468_56786473del, NC_000017.10:g.56786469_56786473del, NC_000017.10:g.56786470_56786473del, NC_000017.10:g.56786471_56786473del, NC_000017.10:g.56786472_56786473del, NC_000017.10:g.56786473del, NC_000017.10:g.56786473dup, NC_000017.10:g.56786472_56786473dup, NC_000017.10:g.56786471_56786473dup, NC_000017.10:g.56786470_56786473dup, NC_000017.10:g.56786469_56786473dup, NC_000017.10:g.56786454_56786473T[26]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000017.10:g.56786456_56786473dup, NC_000017.10:g.56786455_56786473dup, NG_023199.1:g.21500_21511del, NG_023199.1:g.21501_21511del, NG_023199.1:g.21502_21511del, NG_023199.1:g.21504_21511del, NG_023199.1:g.21505_21511del, NG_023199.1:g.21506_21511del, NG_023199.1:g.21507_21511del, NG_023199.1:g.21508_21511del, NG_023199.1:g.21509_21511del, NG_023199.1:g.21510_21511del, NG_023199.1:g.21511del, NG_023199.1:g.21511dup, NG_023199.1:g.21510_21511dup, NG_023199.1:g.21509_21511dup, NG_023199.1:g.21508_21511dup, NG_023199.1:g.21507_21511dup, NG_023199.1:g.21492_21511T[26]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_023199.1:g.21494_21511dup, NG_023199.1:g.21493_21511dup

          5.

          rs1491278007 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->T [Show Flanks]
            Chromosome:
            17:58710318 (GRCh38)
            17:56787680 (GRCh37)
            Canonical SPDI:
            NC_000017.11:58710318::T
            Gene:
            RAD51C (Varview)
            Functional Consequence:
            genic_downstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            T=0./0 (ALFA)
            T=0.000004/1 (TOPMED)
            HGVS:

            6.

            rs1491183844 has merged into rs5821244 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              AAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
              Chromosome:
              17:58712353 (GRCh38)
              17:56789714 (GRCh37)
              Canonical SPDI:
              NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58712344:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
              Gene:
              RAD51C (Varview)
              Functional Consequence:
              intron_variant,genic_downstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              AAAAAAAA=0./0 (ALFA)
              -=0.175/7 (GENOME_DK)
              -=0.3736/1871 (1000Genomes)
              HGVS:
              NC_000017.11:g.58712353_58712365del, NC_000017.11:g.58712354_58712365del, NC_000017.11:g.58712355_58712365del, NC_000017.11:g.58712357_58712365del, NC_000017.11:g.58712358_58712365del, NC_000017.11:g.58712359_58712365del, NC_000017.11:g.58712360_58712365del, NC_000017.11:g.58712361_58712365del, NC_000017.11:g.58712362_58712365del, NC_000017.11:g.58712363_58712365del, NC_000017.11:g.58712364_58712365del, NC_000017.11:g.58712365del, NC_000017.11:g.58712365dup, NC_000017.11:g.58712364_58712365dup, NC_000017.11:g.58712363_58712365dup, NC_000017.11:g.58712362_58712365dup, NC_000017.11:g.58712361_58712365dup, NC_000017.11:g.58712360_58712365dup, NC_000017.11:g.58712359_58712365dup, NC_000017.11:g.58712358_58712365dup, NC_000017.11:g.58712357_58712365dup, NC_000017.11:g.58712346_58712365dup, NC_000017.11:g.58712365_58712366insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.11:g.58712365_58712366insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.11:g.58712365_58712366insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.56789714_56789726del, NC_000017.10:g.56789715_56789726del, NC_000017.10:g.56789716_56789726del, NC_000017.10:g.56789718_56789726del, NC_000017.10:g.56789719_56789726del, NC_000017.10:g.56789720_56789726del, NC_000017.10:g.56789721_56789726del, NC_000017.10:g.56789722_56789726del, NC_000017.10:g.56789723_56789726del, NC_000017.10:g.56789724_56789726del, NC_000017.10:g.56789725_56789726del, NC_000017.10:g.56789726del, NC_000017.10:g.56789726dup, NC_000017.10:g.56789725_56789726dup, NC_000017.10:g.56789724_56789726dup, NC_000017.10:g.56789723_56789726dup, NC_000017.10:g.56789722_56789726dup, NC_000017.10:g.56789721_56789726dup, NC_000017.10:g.56789720_56789726dup, NC_000017.10:g.56789719_56789726dup, NC_000017.10:g.56789718_56789726dup, NC_000017.10:g.56789707_56789726dup, NC_000017.10:g.56789726_56789727insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.56789726_56789727insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.56789726_56789727insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023199.1:g.24752_24764del, NG_023199.1:g.24753_24764del, NG_023199.1:g.24754_24764del, NG_023199.1:g.24756_24764del, NG_023199.1:g.24757_24764del, NG_023199.1:g.24758_24764del, NG_023199.1:g.24759_24764del, NG_023199.1:g.24760_24764del, NG_023199.1:g.24761_24764del, NG_023199.1:g.24762_24764del, NG_023199.1:g.24763_24764del, NG_023199.1:g.24764del, NG_023199.1:g.24764dup, NG_023199.1:g.24763_24764dup, NG_023199.1:g.24762_24764dup, NG_023199.1:g.24761_24764dup, NG_023199.1:g.24760_24764dup, NG_023199.1:g.24759_24764dup, NG_023199.1:g.24758_24764dup, NG_023199.1:g.24757_24764dup, NG_023199.1:g.24756_24764dup, NG_023199.1:g.24745_24764dup, NG_023199.1:g.24764_24765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023199.1:g.24764_24765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023199.1:g.24764_24765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

              7.

              rs1491095875 has merged into rs71143280 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                Chromosome:
                17:58710327 (GRCh38)
                17:56787688 (GRCh37)
                Canonical SPDI:
                NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58710317:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                Gene:
                RAD51C (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Clinical significance:
                benign
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AAAAAAAAAAA=0./0 (ALFA)
                -=0.00899/45 (1000Genomes)
                HGVS:
                NC_000017.11:g.58710327_58710341del, NC_000017.11:g.58710329_58710341del, NC_000017.11:g.58710330_58710341del, NC_000017.11:g.58710331_58710341del, NC_000017.11:g.58710332_58710341del, NC_000017.11:g.58710334_58710341del, NC_000017.11:g.58710335_58710341del, NC_000017.11:g.58710336_58710341del, NC_000017.11:g.58710337_58710341del, NC_000017.11:g.58710338_58710341del, NC_000017.11:g.58710339_58710341del, NC_000017.11:g.58710340_58710341del, NC_000017.11:g.58710341del, NC_000017.11:g.58710341dup, NC_000017.11:g.58710340_58710341dup, NC_000017.11:g.58710339_58710341dup, NC_000017.11:g.58710338_58710341dup, NC_000017.11:g.58710337_58710341dup, NC_000017.11:g.58710336_58710341dup, NC_000017.11:g.58710335_58710341dup, NC_000017.11:g.58710334_58710341dup, NC_000017.11:g.58710332_58710341dup, NC_000017.11:g.58710331_58710341dup, NC_000017.11:g.58710330_58710341dup, NC_000017.11:g.58710329_58710341dup, NC_000017.10:g.56787688_56787702del, NC_000017.10:g.56787690_56787702del, NC_000017.10:g.56787691_56787702del, NC_000017.10:g.56787692_56787702del, NC_000017.10:g.56787693_56787702del, NC_000017.10:g.56787695_56787702del, NC_000017.10:g.56787696_56787702del, NC_000017.10:g.56787697_56787702del, NC_000017.10:g.56787698_56787702del, NC_000017.10:g.56787699_56787702del, NC_000017.10:g.56787700_56787702del, NC_000017.10:g.56787701_56787702del, NC_000017.10:g.56787702del, NC_000017.10:g.56787702dup, NC_000017.10:g.56787701_56787702dup, NC_000017.10:g.56787700_56787702dup, NC_000017.10:g.56787699_56787702dup, NC_000017.10:g.56787698_56787702dup, NC_000017.10:g.56787697_56787702dup, NC_000017.10:g.56787696_56787702dup, NC_000017.10:g.56787695_56787702dup, NC_000017.10:g.56787693_56787702dup, NC_000017.10:g.56787692_56787702dup, NC_000017.10:g.56787691_56787702dup, NC_000017.10:g.56787690_56787702dup, NG_023199.1:g.22726_22740del, NG_023199.1:g.22728_22740del, NG_023199.1:g.22729_22740del, NG_023199.1:g.22730_22740del, NG_023199.1:g.22731_22740del, NG_023199.1:g.22733_22740del, NG_023199.1:g.22734_22740del, NG_023199.1:g.22735_22740del, NG_023199.1:g.22736_22740del, NG_023199.1:g.22737_22740del, NG_023199.1:g.22738_22740del, NG_023199.1:g.22739_22740del, NG_023199.1:g.22740del, NG_023199.1:g.22740dup, NG_023199.1:g.22739_22740dup, NG_023199.1:g.22738_22740dup, NG_023199.1:g.22737_22740dup, NG_023199.1:g.22736_22740dup, NG_023199.1:g.22735_22740dup, NG_023199.1:g.22734_22740dup, NG_023199.1:g.22733_22740dup, NG_023199.1:g.22731_22740dup, NG_023199.1:g.22730_22740dup, NG_023199.1:g.22729_22740dup, NG_023199.1:g.22728_22740dup

                8.

                rs1491055304 has merged into rs34546660 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                  Chromosome:
                  17:58691683 (GRCh38)
                  17:56769044 (GRCh37)
                  Canonical SPDI:
                  NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58691666:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                  Gene:
                  RAD51C (Varview), TEX14 (Varview), IGBP1P2 (Varview)
                  Functional Consequence:
                  upstream_transcript_variant,2KB_upstream_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAAAAAAAAAAAA=0./0 (ALFA)
                  HGVS:
                  NC_000017.11:g.58691683_58691685del, NC_000017.11:g.58691684_58691685del, NC_000017.11:g.58691685del, NC_000017.11:g.58691685dup, NC_000017.11:g.58691684_58691685dup, NC_000017.11:g.58691683_58691685dup, NC_000017.11:g.58691682_58691685dup, NC_000017.11:g.58691681_58691685dup, NC_000017.11:g.58691680_58691685dup, NC_000017.11:g.58691685_58691686insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.56769044_56769046del, NC_000017.10:g.56769045_56769046del, NC_000017.10:g.56769046del, NC_000017.10:g.56769046dup, NC_000017.10:g.56769045_56769046dup, NC_000017.10:g.56769044_56769046dup, NC_000017.10:g.56769043_56769046dup, NC_000017.10:g.56769042_56769046dup, NC_000017.10:g.56769041_56769046dup, NC_000017.10:g.56769046_56769047insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_047169.1:g.5411_5413del, NG_047169.1:g.5412_5413del, NG_047169.1:g.5413del, NG_047169.1:g.5413dup, NG_047169.1:g.5412_5413dup, NG_047169.1:g.5411_5413dup, NG_047169.1:g.5410_5413dup, NG_047169.1:g.5409_5413dup, NG_047169.1:g.5408_5413dup, NG_047169.1:g.5413_5414insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023199.1:g.4082_4084del, NG_023199.1:g.4083_4084del, NG_023199.1:g.4084del, NG_023199.1:g.4084dup, NG_023199.1:g.4083_4084dup, NG_023199.1:g.4082_4084dup, NG_023199.1:g.4081_4084dup, NG_023199.1:g.4080_4084dup, NG_023199.1:g.4079_4084dup, NG_023199.1:g.4084_4085insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                  9.

                  rs1491045596 has merged into rs34530914 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    17:58697551 (GRCh38)
                    17:56774912 (GRCh37)
                    Canonical SPDI:
                    NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:58697540:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    RAD51C (Varview)
                    Functional Consequence:
                    genic_downstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAAAAAA=0./0 (ALFA)
                    -=0.000004/1 (TOPMED)
                    A=0.4/16 (GENOME_DK)
                    HGVS:
                    NC_000017.11:g.58697551_58697557del, NC_000017.11:g.58697555_58697557del, NC_000017.11:g.58697556_58697557del, NC_000017.11:g.58697557del, NC_000017.11:g.58697557dup, NC_000017.11:g.58697556_58697557dup, NC_000017.11:g.58697555_58697557dup, NC_000017.11:g.58697554_58697557dup, NC_000017.11:g.58697553_58697557dup, NC_000017.10:g.56774912_56774918del, NC_000017.10:g.56774916_56774918del, NC_000017.10:g.56774917_56774918del, NC_000017.10:g.56774918del, NC_000017.10:g.56774918dup, NC_000017.10:g.56774917_56774918dup, NC_000017.10:g.56774916_56774918dup, NC_000017.10:g.56774915_56774918dup, NC_000017.10:g.56774914_56774918dup, NG_023199.1:g.9950_9956del, NG_023199.1:g.9954_9956del, NG_023199.1:g.9955_9956del, NG_023199.1:g.9956del, NG_023199.1:g.9956dup, NG_023199.1:g.9955_9956dup, NG_023199.1:g.9954_9956dup, NG_023199.1:g.9953_9956dup, NG_023199.1:g.9952_9956dup

                    10.

                    rs1491011975 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      TA>- [Show Flanks]
                      Chromosome:
                      17:58720427 (GRCh38)
                      17:56797788 (GRCh37)
                      Canonical SPDI:
                      NC_000017.11:58720425:ATA:A
                      Gene:
                      RAD51C (Varview)
                      Functional Consequence:
                      genic_downstream_transcript_variant,intron_variant
                      Clinical significance:
                      likely-benign
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0.002529/30 (ALFA)
                      -=0.003914/532 (GnomAD)
                      HGVS:

                      11.

                      rs1490979983 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>C [Show Flanks]
                        Chromosome:
                        17:58713547 (GRCh38)
                        17:56790908 (GRCh37)
                        Canonical SPDI:
                        NC_000017.11:58713546:A:C
                        Gene:
                        RAD51C (Varview)
                        Functional Consequence:
                        genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        C=0./0 (ALFA)
                        C=0./0 (GnomAD)
                        C=0.000468/3 (1000Genomes)
                        HGVS:

                        12.

                        rs1490905207 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          ->T [Show Flanks]
                          Chromosome:
                          17:58707647 (GRCh38)
                          17:56785009 (GRCh37)
                          Canonical SPDI:
                          NC_000017.11:58707647:T:TT
                          Gene:
                          RAD51C (Varview)
                          Functional Consequence:
                          genic_downstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          TT=0./0 (ALFA)
                          T=0.000007/1 (GnomAD)
                          T=0.000019/5 (TOPMED)
                          HGVS:

                          13.

                          rs1490876719 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>G [Show Flanks]
                            Chromosome:
                            17:58722578 (GRCh38)
                            17:56799939 (GRCh37)
                            Canonical SPDI:
                            NC_000017.11:58722577:T:G
                            Gene:
                            RAD51C (Varview)
                            Functional Consequence:
                            genic_downstream_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1490850231 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              17:58721440 (GRCh38)
                              17:56798801 (GRCh37)
                              Canonical SPDI:
                              NC_000017.11:58721439:T:C
                              Gene:
                              RAD51C (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (TOPMED)
                              C=0.000007/1 (GnomAD)
                              HGVS:

                              15.

                              rs1490808929 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>A [Show Flanks]
                                Chromosome:
                                17:58714197 (GRCh38)
                                17:56791558 (GRCh37)
                                Canonical SPDI:
                                NC_000017.11:58714196:C:A
                                Gene:
                                RAD51C (Varview)
                                Functional Consequence:
                                genic_downstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0./0 (ALFA)
                                A=0.000034/9 (TOPMED)
                                A=0.000043/6 (GnomAD)
                                HGVS:

                                16.

                                rs1490757492 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>G [Show Flanks]
                                  Chromosome:
                                  17:58699451 (GRCh38)
                                  17:56776812 (GRCh37)
                                  Canonical SPDI:
                                  NC_000017.11:58699450:T:G
                                  Gene:
                                  RAD51C (Varview)
                                  Functional Consequence:
                                  genic_downstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000008/2 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490731421 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    17:58700400 (GRCh38)
                                    17:56777761 (GRCh37)
                                    Canonical SPDI:
                                    NC_000017.11:58700399:G:A
                                    Gene:
                                    RAD51C (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    A=0./0 (ALFA)
                                    HGVS:

                                    18.

                                    rs1490615062 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>T [Show Flanks]
                                      Chromosome:
                                      17:58730701 (GRCh38)
                                      17:56808062 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:58730700:A:T
                                      Gene:
                                      RAD51C (Varview), LOC105371843 (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0.000071/1 (ALFA)
                                      T=0.000015/4 (TOPMED)
                                      T=0.000036/5 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490594603 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>G [Show Flanks]
                                        Chromosome:
                                        17:58699153 (GRCh38)
                                        17:56776514 (GRCh37)
                                        Canonical SPDI:
                                        NC_000017.11:58699152:T:G
                                        Gene:
                                        RAD51C (Varview)
                                        Functional Consequence:
                                        genic_downstream_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1490538074 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          17:58712750 (GRCh38)
                                          17:56790111 (GRCh37)
                                          Canonical SPDI:
                                          NC_000017.11:58712749:G:A
                                          Gene:
                                          RAD51C (Varview)
                                          Functional Consequence:
                                          genic_downstream_transcript_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:

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