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1.

rs1491532357 has merged into rs34715101 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    11:4133993 (GRCh38)
    11:4155223 (GRCh37)
    Canonical SPDI:
    NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4133980:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    RRM1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTTTTT=0./0 (ALFA)
    HGVS:
    NC_000011.10:g.4133993_4134004del, NC_000011.10:g.4133994_4134004del, NC_000011.10:g.4133995_4134004del, NC_000011.10:g.4133996_4134004del, NC_000011.10:g.4133998_4134004del, NC_000011.10:g.4133999_4134004del, NC_000011.10:g.4134000_4134004del, NC_000011.10:g.4134001_4134004del, NC_000011.10:g.4134002_4134004del, NC_000011.10:g.4134003_4134004del, NC_000011.10:g.4134004del, NC_000011.10:g.4134004dup, NC_000011.10:g.4134003_4134004dup, NC_000011.10:g.4134002_4134004dup, NC_000011.10:g.4134001_4134004dup, NC_000011.10:g.4134000_4134004dup, NC_000011.10:g.4133999_4134004dup, NC_000011.10:g.4133998_4134004dup, NC_000011.10:g.4133997_4134004dup, NC_000011.10:g.4133996_4134004dup, NC_000011.10:g.4133995_4134004dup, NC_000011.10:g.4133994_4134004dup, NC_000011.10:g.4133993_4134004dup, NC_000011.10:g.4133992_4134004dup, NC_000011.10:g.4133990_4134004dup, NC_000011.10:g.4133989_4134004dup, NC_000011.10:g.4133988_4134004dup, NC_000011.10:g.4133982_4134004dup, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.4134004_4134005insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155223_4155234del, NC_000011.9:g.4155224_4155234del, NC_000011.9:g.4155225_4155234del, NC_000011.9:g.4155226_4155234del, NC_000011.9:g.4155228_4155234del, NC_000011.9:g.4155229_4155234del, NC_000011.9:g.4155230_4155234del, NC_000011.9:g.4155231_4155234del, NC_000011.9:g.4155232_4155234del, NC_000011.9:g.4155233_4155234del, NC_000011.9:g.4155234del, NC_000011.9:g.4155234dup, NC_000011.9:g.4155233_4155234dup, NC_000011.9:g.4155232_4155234dup, NC_000011.9:g.4155231_4155234dup, NC_000011.9:g.4155230_4155234dup, NC_000011.9:g.4155229_4155234dup, NC_000011.9:g.4155228_4155234dup, NC_000011.9:g.4155227_4155234dup, NC_000011.9:g.4155226_4155234dup, NC_000011.9:g.4155225_4155234dup, NC_000011.9:g.4155224_4155234dup, NC_000011.9:g.4155223_4155234dup, NC_000011.9:g.4155222_4155234dup, NC_000011.9:g.4155220_4155234dup, NC_000011.9:g.4155219_4155234dup, NC_000011.9:g.4155218_4155234dup, NC_000011.9:g.4155212_4155234dup, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4155234_4155235insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44300_44311del, NG_027992.2:g.44301_44311del, NG_027992.2:g.44302_44311del, NG_027992.2:g.44303_44311del, NG_027992.2:g.44305_44311del, NG_027992.2:g.44306_44311del, NG_027992.2:g.44307_44311del, NG_027992.2:g.44308_44311del, NG_027992.2:g.44309_44311del, NG_027992.2:g.44310_44311del, NG_027992.2:g.44311del, NG_027992.2:g.44311dup, NG_027992.2:g.44310_44311dup, NG_027992.2:g.44309_44311dup, NG_027992.2:g.44308_44311dup, NG_027992.2:g.44307_44311dup, NG_027992.2:g.44306_44311dup, NG_027992.2:g.44305_44311dup, NG_027992.2:g.44304_44311dup, NG_027992.2:g.44303_44311dup, NG_027992.2:g.44302_44311dup, NG_027992.2:g.44301_44311dup, NG_027992.2:g.44300_44311dup, NG_027992.2:g.44299_44311dup, NG_027992.2:g.44297_44311dup, NG_027992.2:g.44296_44311dup, NG_027992.2:g.44295_44311dup, NG_027992.2:g.44289_44311dup, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.44311_44312insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

    2.

    rs1491327790 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->TAT [Show Flanks]
      Chromosome:
      11:4126046 (GRCh38)
      11:4147277 (GRCh37)
      Canonical SPDI:
      NC_000011.10:4126046:TAT:TATTAT
      Gene:
      RRM1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TATTAT=0./0 (ALFA)
      TAT=0.000007/1 (GnomAD)
      TAT=0.000015/4 (TOPMED)
      HGVS:

      3.

      rs1491325130 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TT>-,TTTT [Show Flanks]
        Chromosome:
        11:4130066 (GRCh38)
        11:4151296 (GRCh37)
        Canonical SPDI:
        NC_000011.10:4130064:TTT:T,NC_000011.10:4130064:TTT:TTTTT
        Gene:
        RRM1 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.00043/7 (ALFA)
        -=0.0012/2 (Korea1K)
        -=0.00222/37 (TOMMO)
        HGVS:

        4.

        rs1491305459 has merged into rs34264302 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
          Chromosome:
          11:4103960 (GRCh38)
          11:4125190 (GRCh37)
          Canonical SPDI:
          NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4103946:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
          Gene:
          RRM1 (Varview)
          Functional Consequence:
          intron_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          AAAAAAAAAAAAAA=0./0 (ALFA)
          AA=0.1863/933 (1000Genomes)
          HGVS:
          NC_000011.10:g.4103960_4103968del, NC_000011.10:g.4103961_4103968del, NC_000011.10:g.4103963_4103968del, NC_000011.10:g.4103964_4103968del, NC_000011.10:g.4103965_4103968del, NC_000011.10:g.4103966_4103968del, NC_000011.10:g.4103967_4103968del, NC_000011.10:g.4103968del, NC_000011.10:g.4103968dup, NC_000011.10:g.4103967_4103968dup, NC_000011.10:g.4103966_4103968dup, NC_000011.10:g.4103963_4103968dup, NC_000011.9:g.4125190_4125198del, NC_000011.9:g.4125191_4125198del, NC_000011.9:g.4125193_4125198del, NC_000011.9:g.4125194_4125198del, NC_000011.9:g.4125195_4125198del, NC_000011.9:g.4125196_4125198del, NC_000011.9:g.4125197_4125198del, NC_000011.9:g.4125198del, NC_000011.9:g.4125198dup, NC_000011.9:g.4125197_4125198dup, NC_000011.9:g.4125196_4125198dup, NC_000011.9:g.4125193_4125198dup, NG_027992.2:g.14267_14275del, NG_027992.2:g.14268_14275del, NG_027992.2:g.14270_14275del, NG_027992.2:g.14271_14275del, NG_027992.2:g.14272_14275del, NG_027992.2:g.14273_14275del, NG_027992.2:g.14274_14275del, NG_027992.2:g.14275del, NG_027992.2:g.14275dup, NG_027992.2:g.14274_14275dup, NG_027992.2:g.14273_14275dup, NG_027992.2:g.14270_14275dup

          5.

          rs1491287200 [Homo sapiens]
            Variant type:
            SNV:
            Alleles:
            ->GTTTT
            Chromosome:
            no mapping
            Canonical SPDI:

            6.

            rs1491287037 has merged into rs1221330899 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              AAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
              Chromosome:
              11:4097292 (GRCh38)
              11:4118522 (GRCh37)
              Canonical SPDI:
              NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:4097278:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
              Gene:
              RRM1 (Varview)
              Functional Consequence:
              intron_variant,genic_upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              AAAAAAAAAAAAAA=0./0 (ALFA)
              HGVS:
              NC_000011.10:g.4097292_4097301del, NC_000011.10:g.4097293_4097301del, NC_000011.10:g.4097295_4097301del, NC_000011.10:g.4097296_4097301del, NC_000011.10:g.4097297_4097301del, NC_000011.10:g.4097298_4097301del, NC_000011.10:g.4097299_4097301del, NC_000011.10:g.4097300_4097301del, NC_000011.10:g.4097301del, NC_000011.10:g.4097301dup, NC_000011.10:g.4097300_4097301dup, NC_000011.10:g.4097299_4097301dup, NC_000011.10:g.4097298_4097301dup, NC_000011.10:g.4097296_4097301dup, NC_000011.10:g.4097295_4097301dup, NC_000011.10:g.4097289_4097301dup, NC_000011.9:g.4118522_4118531del, NC_000011.9:g.4118523_4118531del, NC_000011.9:g.4118525_4118531del, NC_000011.9:g.4118526_4118531del, NC_000011.9:g.4118527_4118531del, NC_000011.9:g.4118528_4118531del, NC_000011.9:g.4118529_4118531del, NC_000011.9:g.4118530_4118531del, NC_000011.9:g.4118531del, NC_000011.9:g.4118531dup, NC_000011.9:g.4118530_4118531dup, NC_000011.9:g.4118529_4118531dup, NC_000011.9:g.4118528_4118531dup, NC_000011.9:g.4118526_4118531dup, NC_000011.9:g.4118525_4118531dup, NC_000011.9:g.4118519_4118531dup, NG_027992.2:g.7599_7608del, NG_027992.2:g.7600_7608del, NG_027992.2:g.7602_7608del, NG_027992.2:g.7603_7608del, NG_027992.2:g.7604_7608del, NG_027992.2:g.7605_7608del, NG_027992.2:g.7606_7608del, NG_027992.2:g.7607_7608del, NG_027992.2:g.7608del, NG_027992.2:g.7608dup, NG_027992.2:g.7607_7608dup, NG_027992.2:g.7606_7608dup, NG_027992.2:g.7605_7608dup, NG_027992.2:g.7603_7608dup, NG_027992.2:g.7602_7608dup, NG_027992.2:g.7596_7608dup

              7.

              rs1491252235 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                CA>- [Show Flanks]
                Chromosome:
                11:4097278 (GRCh38)
                11:4118508 (GRCh37)
                Canonical SPDI:
                NC_000011.10:4097277:CA:
                Gene:
                RRM1 (Varview)
                Functional Consequence:
                genic_upstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                -=0.00135/16 (ALFA)
                HGVS:

                8.

                rs1491242040 has merged into rs55705631 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTTTTTTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  11:4105587 (GRCh38)
                  11:4126817 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4105578:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  RRM1 (Varview)
                  Functional Consequence:
                  intron_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTT=0./0 (ALFA)
                  HGVS:
                  NC_000011.10:g.4105587_4105598del, NC_000011.10:g.4105588_4105598del, NC_000011.10:g.4105589_4105598del, NC_000011.10:g.4105590_4105598del, NC_000011.10:g.4105592_4105598del, NC_000011.10:g.4105593_4105598del, NC_000011.10:g.4105594_4105598del, NC_000011.10:g.4105595_4105598del, NC_000011.10:g.4105596_4105598del, NC_000011.10:g.4105597_4105598del, NC_000011.10:g.4105598del, NC_000011.10:g.4105598dup, NC_000011.10:g.4105597_4105598dup, NC_000011.10:g.4105596_4105598dup, NC_000011.10:g.4105595_4105598dup, NC_000011.10:g.4105594_4105598dup, NC_000011.10:g.4105593_4105598dup, NC_000011.10:g.4105592_4105598dup, NC_000011.10:g.4105591_4105598dup, NC_000011.10:g.4105590_4105598dup, NC_000011.10:g.4105586_4105598dup, NC_000011.10:g.4105585_4105598dup, NC_000011.10:g.4105598_4105599insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.4126817_4126828del, NC_000011.9:g.4126818_4126828del, NC_000011.9:g.4126819_4126828del, NC_000011.9:g.4126820_4126828del, NC_000011.9:g.4126822_4126828del, NC_000011.9:g.4126823_4126828del, NC_000011.9:g.4126824_4126828del, NC_000011.9:g.4126825_4126828del, NC_000011.9:g.4126826_4126828del, NC_000011.9:g.4126827_4126828del, NC_000011.9:g.4126828del, NC_000011.9:g.4126828dup, NC_000011.9:g.4126827_4126828dup, NC_000011.9:g.4126826_4126828dup, NC_000011.9:g.4126825_4126828dup, NC_000011.9:g.4126824_4126828dup, NC_000011.9:g.4126823_4126828dup, NC_000011.9:g.4126822_4126828dup, NC_000011.9:g.4126821_4126828dup, NC_000011.9:g.4126820_4126828dup, NC_000011.9:g.4126816_4126828dup, NC_000011.9:g.4126815_4126828dup, NC_000011.9:g.4126828_4126829insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027992.2:g.15894_15905del, NG_027992.2:g.15895_15905del, NG_027992.2:g.15896_15905del, NG_027992.2:g.15897_15905del, NG_027992.2:g.15899_15905del, NG_027992.2:g.15900_15905del, NG_027992.2:g.15901_15905del, NG_027992.2:g.15902_15905del, NG_027992.2:g.15903_15905del, NG_027992.2:g.15904_15905del, NG_027992.2:g.15905del, NG_027992.2:g.15905dup, NG_027992.2:g.15904_15905dup, NG_027992.2:g.15903_15905dup, NG_027992.2:g.15902_15905dup, NG_027992.2:g.15901_15905dup, NG_027992.2:g.15900_15905dup, NG_027992.2:g.15899_15905dup, NG_027992.2:g.15898_15905dup, NG_027992.2:g.15897_15905dup, NG_027992.2:g.15893_15905dup, NG_027992.2:g.15892_15905dup, NG_027992.2:g.15905_15906insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                  9.

                  rs1491196087 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    TA>- [Show Flanks]
                    Chromosome:
                    11:4126049 (GRCh38)
                    11:4147279 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:4126045:ATATA:ATA
                    Gene:
                    RRM1 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    ATA=0./0 (ALFA)
                    -=0.000011/3 (TOPMED)
                    HGVS:

                    10.

                    rs1491155581 has merged into rs869309117 [Homo sapiens]
                      Variant type:
                      INS
                      Alleles:
                      ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATATATATATATA,ATATATATATATATATATATATATA,ATATATATATATATATATATATATATA,ATATATATATATATATATATATATATATA,ATATATATATATATATATATATATATATATA,ATATATATATATATATATATATATATATATATA,ATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
                      Chromosome:
                      11:4130087 (GRCh38)
                      11:4151318 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:4130087::A,NC_000011.10:4130087::ATA,NC_000011.10:4130087::ATATA,NC_000011.10:4130087::ATATATA,NC_000011.10:4130087::ATATATATA,NC_000011.10:4130087::ATATATATATA,NC_000011.10:4130087::ATATATATATATA,NC_000011.10:4130087::ATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATATATATATA,NC_000011.10:4130087::ATATATATATATATATATATATATATATATATATATATATATATA
                      Gene:
                      RRM1 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      ATA=0./0 (ALFA)
                      HGVS:
                      NC_000011.10:g.4130087_4130088insA, NC_000011.10:g.4130087_4130088insATA, NC_000011.10:g.4130087_4130088insATATA, NC_000011.10:g.4130087_4130088insATATATA, NC_000011.10:g.4130087_4130088insATATATATA, NC_000011.10:g.4130087_4130088insATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATATATATATA, NC_000011.10:g.4130087_4130088insATATATATATATATATATATATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insA, NC_000011.9:g.4151317_4151318insATA, NC_000011.9:g.4151317_4151318insATATA, NC_000011.9:g.4151317_4151318insATATATA, NC_000011.9:g.4151317_4151318insATATATATA, NC_000011.9:g.4151317_4151318insATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATATATATATA, NC_000011.9:g.4151317_4151318insATATATATATATATATATATATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insA, NG_027992.2:g.40394_40395insATA, NG_027992.2:g.40394_40395insATATA, NG_027992.2:g.40394_40395insATATATA, NG_027992.2:g.40394_40395insATATATATA, NG_027992.2:g.40394_40395insATATATATATA, NG_027992.2:g.40394_40395insATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATATATATATA, NG_027992.2:g.40394_40395insATATATATATATATATATATATATATATATATATATATATATATA

                      11.

                      rs1491139273 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->G [Show Flanks]
                        Chromosome:
                        11:4116975 (GRCh38)
                        11:4138206 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:4116975:G:GG
                        Gene:
                        RRM1 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        GG=0./0 (ALFA)
                        G=0.000007/1 (GnomAD)
                        G=0.000011/3 (TOPMED)
                        HGVS:

                        12.

                        rs1491089673 has merged into rs796657105 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          TTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                          Chromosome:
                          11:4130093 (GRCh38)
                          11:4151323 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
                          Gene:
                          RRM1 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          TTTTTTT=0./0 (ALFA)
                          HGVS:
                          NC_000011.10:g.4130093_4130104del, NC_000011.10:g.4130094_4130104del, NC_000011.10:g.4130095_4130104del, NC_000011.10:g.4130096_4130104del, NC_000011.10:g.4130097_4130104del, NC_000011.10:g.4130098_4130104del, NC_000011.10:g.4130099_4130104del, NC_000011.10:g.4130100_4130104del, NC_000011.10:g.4130101_4130104del, NC_000011.10:g.4130102_4130104del, NC_000011.10:g.4130103_4130104del, NC_000011.10:g.4130104del, NC_000011.10:g.4130104dup, NC_000011.10:g.4130103_4130104dup, NC_000011.10:g.4130102_4130104dup, NC_000011.10:g.4130101_4130104dup, NC_000011.10:g.4130100_4130104dup, NC_000011.10:g.4130099_4130104dup, NC_000011.10:g.4130098_4130104dup, NC_000011.10:g.4130097_4130104dup, NC_000011.10:g.4130096_4130104dup, NC_000011.10:g.4130095_4130104dup, NC_000011.9:g.4151323_4151334del, NC_000011.9:g.4151324_4151334del, NC_000011.9:g.4151325_4151334del, NC_000011.9:g.4151326_4151334del, NC_000011.9:g.4151327_4151334del, NC_000011.9:g.4151328_4151334del, NC_000011.9:g.4151329_4151334del, NC_000011.9:g.4151330_4151334del, NC_000011.9:g.4151331_4151334del, NC_000011.9:g.4151332_4151334del, NC_000011.9:g.4151333_4151334del, NC_000011.9:g.4151334del, NC_000011.9:g.4151334dup, NC_000011.9:g.4151333_4151334dup, NC_000011.9:g.4151332_4151334dup, NC_000011.9:g.4151331_4151334dup, NC_000011.9:g.4151330_4151334dup, NC_000011.9:g.4151329_4151334dup, NC_000011.9:g.4151328_4151334dup, NC_000011.9:g.4151327_4151334dup, NC_000011.9:g.4151326_4151334dup, NC_000011.9:g.4151325_4151334dup, NG_027992.2:g.40400_40411del, NG_027992.2:g.40401_40411del, NG_027992.2:g.40402_40411del, NG_027992.2:g.40403_40411del, NG_027992.2:g.40404_40411del, NG_027992.2:g.40405_40411del, NG_027992.2:g.40406_40411del, NG_027992.2:g.40407_40411del, NG_027992.2:g.40408_40411del, NG_027992.2:g.40409_40411del, NG_027992.2:g.40410_40411del, NG_027992.2:g.40411del, NG_027992.2:g.40411dup, NG_027992.2:g.40410_40411dup, NG_027992.2:g.40409_40411dup, NG_027992.2:g.40408_40411dup, NG_027992.2:g.40407_40411dup, NG_027992.2:g.40406_40411dup, NG_027992.2:g.40405_40411dup, NG_027992.2:g.40404_40411dup, NG_027992.2:g.40403_40411dup, NG_027992.2:g.40402_40411dup

                          13.

                          rs1490834290 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            11:4097278 (GRCh38)
                            11:4118508 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:4097277:C:A
                            Gene:
                            RRM1 (Varview)
                            Functional Consequence:
                            genic_upstream_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            A=0.00365/49 (ALFA)
                            A=0.10905/318 (KOREAN)
                            HGVS:

                            14.

                            rs1490770692 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              11:4113450 (GRCh38)
                              11:4134680 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:4113449:G:A
                              Gene:
                              RRM1 (Varview)
                              Functional Consequence:
                              genic_upstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              A=0./0 (ALFA)
                              A=0.000008/2 (TOPMED)
                              HGVS:

                              15.

                              rs1490677795 has merged into rs796657105 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                Chromosome:
                                11:4130093 (GRCh38)
                                11:4151323 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:4130086:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                Gene:
                                RRM1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TTTTTTT=0./0 (ALFA)
                                HGVS:
                                NC_000011.10:g.4130093_4130104del, NC_000011.10:g.4130094_4130104del, NC_000011.10:g.4130095_4130104del, NC_000011.10:g.4130096_4130104del, NC_000011.10:g.4130097_4130104del, NC_000011.10:g.4130098_4130104del, NC_000011.10:g.4130099_4130104del, NC_000011.10:g.4130100_4130104del, NC_000011.10:g.4130101_4130104del, NC_000011.10:g.4130102_4130104del, NC_000011.10:g.4130103_4130104del, NC_000011.10:g.4130104del, NC_000011.10:g.4130104dup, NC_000011.10:g.4130103_4130104dup, NC_000011.10:g.4130102_4130104dup, NC_000011.10:g.4130101_4130104dup, NC_000011.10:g.4130100_4130104dup, NC_000011.10:g.4130099_4130104dup, NC_000011.10:g.4130098_4130104dup, NC_000011.10:g.4130097_4130104dup, NC_000011.10:g.4130096_4130104dup, NC_000011.10:g.4130095_4130104dup, NC_000011.9:g.4151323_4151334del, NC_000011.9:g.4151324_4151334del, NC_000011.9:g.4151325_4151334del, NC_000011.9:g.4151326_4151334del, NC_000011.9:g.4151327_4151334del, NC_000011.9:g.4151328_4151334del, NC_000011.9:g.4151329_4151334del, NC_000011.9:g.4151330_4151334del, NC_000011.9:g.4151331_4151334del, NC_000011.9:g.4151332_4151334del, NC_000011.9:g.4151333_4151334del, NC_000011.9:g.4151334del, NC_000011.9:g.4151334dup, NC_000011.9:g.4151333_4151334dup, NC_000011.9:g.4151332_4151334dup, NC_000011.9:g.4151331_4151334dup, NC_000011.9:g.4151330_4151334dup, NC_000011.9:g.4151329_4151334dup, NC_000011.9:g.4151328_4151334dup, NC_000011.9:g.4151327_4151334dup, NC_000011.9:g.4151326_4151334dup, NC_000011.9:g.4151325_4151334dup, NG_027992.2:g.40400_40411del, NG_027992.2:g.40401_40411del, NG_027992.2:g.40402_40411del, NG_027992.2:g.40403_40411del, NG_027992.2:g.40404_40411del, NG_027992.2:g.40405_40411del, NG_027992.2:g.40406_40411del, NG_027992.2:g.40407_40411del, NG_027992.2:g.40408_40411del, NG_027992.2:g.40409_40411del, NG_027992.2:g.40410_40411del, NG_027992.2:g.40411del, NG_027992.2:g.40411dup, NG_027992.2:g.40410_40411dup, NG_027992.2:g.40409_40411dup, NG_027992.2:g.40408_40411dup, NG_027992.2:g.40407_40411dup, NG_027992.2:g.40406_40411dup, NG_027992.2:g.40405_40411dup, NG_027992.2:g.40404_40411dup, NG_027992.2:g.40403_40411dup, NG_027992.2:g.40402_40411dup

                                16.

                                rs1490622810 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ->T [Show Flanks]
                                  Chromosome:
                                  11:4112804 (GRCh38)
                                  11:4134035 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:4112804:T:TT
                                  Gene:
                                  RRM1 (Varview)
                                  Functional Consequence:
                                  genic_upstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  TT=0./0 (ALFA)
                                  HGVS:

                                  17.

                                  rs1490589204 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ATATATATTTTTTTTT>- [Show Flanks]
                                    Chromosome:
                                    11:4130080 (GRCh38)
                                    11:4151310 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:4130078:TATATATATTTTTTTTT:T
                                    Gene:
                                    RRM1 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    -=0.00001/1 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1490580497 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>C [Show Flanks]
                                      Chromosome:
                                      11:4101967 (GRCh38)
                                      11:4123197 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:4101966:A:C
                                      Gene:
                                      RRM1 (Varview)
                                      Functional Consequence:
                                      genic_upstream_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000042/11 (TOPMED)
                                      C=0.00005/7 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490439918 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        11:4137891 (GRCh38)
                                        11:4159121 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:4137890:C:T
                                        Gene:
                                        RRM1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0./0 (ALFA)
                                        HGVS:

                                        20.

                                        rs1490337087 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TGTCCT>- [Show Flanks]
                                          Chromosome:
                                          11:4111775 (GRCh38)
                                          11:4133005 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:4111773:TTGTCCT:T
                                          Gene:
                                          RRM1 (Varview)
                                          Functional Consequence:
                                          genic_upstream_transcript_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          T=0./0 (ALFA)
                                          -=0.000014/2 (GnomAD)
                                          HGVS:

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