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Items: 1 to 20 of 38634

1.

rs1491553050 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    CA>- [Show Flanks]
    Chromosome:
    15:31093260 (GRCh38)
    15:31385463 (GRCh37)
    Canonical SPDI:
    NC_000015.10:31093259:CA:
    Gene:
    TRPM1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0.00497/59 (ALFA)
    -=0.00336/93 (TOMMO)
    HGVS:

    2.

    rs1491533231 has merged into rs34790478 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAAAAAAAAAAA>-,A,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
      Chromosome:
      15:31093274 (GRCh38)
      15:31385477 (GRCh37)
      Canonical SPDI:
      NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31093260:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
      Gene:
      TRPM1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAAAAAA=0./0 (ALFA)
      HGVS:
      NC_000015.10:g.31093274_31093286del, NC_000015.10:g.31093275_31093286del, NC_000015.10:g.31093278_31093286del, NC_000015.10:g.31093280_31093286del, NC_000015.10:g.31093281_31093286del, NC_000015.10:g.31093282_31093286del, NC_000015.10:g.31093283_31093286del, NC_000015.10:g.31093284_31093286del, NC_000015.10:g.31093285_31093286del, NC_000015.10:g.31093286del, NC_000015.10:g.31093286dup, NC_000015.10:g.31093285_31093286dup, NC_000015.10:g.31093284_31093286dup, NC_000015.10:g.31093283_31093286dup, NC_000015.10:g.31093282_31093286dup, NC_000015.10:g.31093281_31093286dup, NC_000015.10:g.31093278_31093286dup, NC_000015.10:g.31093264_31093286dup, NC_000015.10:g.31093261_31093286A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000015.9:g.31385477_31385489del, NC_000015.9:g.31385478_31385489del, NC_000015.9:g.31385481_31385489del, NC_000015.9:g.31385483_31385489del, NC_000015.9:g.31385484_31385489del, NC_000015.9:g.31385485_31385489del, NC_000015.9:g.31385486_31385489del, NC_000015.9:g.31385487_31385489del, NC_000015.9:g.31385488_31385489del, NC_000015.9:g.31385489del, NC_000015.9:g.31385489dup, NC_000015.9:g.31385488_31385489dup, NC_000015.9:g.31385487_31385489dup, NC_000015.9:g.31385486_31385489dup, NC_000015.9:g.31385485_31385489dup, NC_000015.9:g.31385484_31385489dup, NC_000015.9:g.31385481_31385489dup, NC_000015.9:g.31385467_31385489dup, NC_000015.9:g.31385464_31385489A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016453.2:g.73001_73013del, NG_016453.2:g.73002_73013del, NG_016453.2:g.73005_73013del, NG_016453.2:g.73007_73013del, NG_016453.2:g.73008_73013del, NG_016453.2:g.73009_73013del, NG_016453.2:g.73010_73013del, NG_016453.2:g.73011_73013del, NG_016453.2:g.73012_73013del, NG_016453.2:g.73013del, NG_016453.2:g.73013dup, NG_016453.2:g.73012_73013dup, NG_016453.2:g.73011_73013dup, NG_016453.2:g.73010_73013dup, NG_016453.2:g.73009_73013dup, NG_016453.2:g.73008_73013dup, NG_016453.2:g.73005_73013dup, NG_016453.2:g.72991_73013dup, NG_016453.2:g.72988_73013T[31]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_011332701.1:g.3266580dup, NW_011332701.1:g.3266569_3266580del, NW_011332701.1:g.3266570_3266580del, NW_011332701.1:g.3266573_3266580del, NW_011332701.1:g.3266575_3266580del, NW_011332701.1:g.3266576_3266580del, NW_011332701.1:g.3266577_3266580del, NW_011332701.1:g.3266578_3266580del, NW_011332701.1:g.3266579_3266580del, NW_011332701.1:g.3266580del, NW_011332701.1:g.3266579_3266580dup, NW_011332701.1:g.3266578_3266580dup, NW_011332701.1:g.3266577_3266580dup, NW_011332701.1:g.3266576_3266580dup, NW_011332701.1:g.3266575_3266580dup, NW_011332701.1:g.3266574_3266580dup, NW_011332701.1:g.3266571_3266580dup, NW_011332701.1:g.3266557_3266580dup, NW_011332701.1:g.3266556_3266580A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187660.1:g.3379032dup, NT_187660.1:g.3379021_3379032del, NT_187660.1:g.3379022_3379032del, NT_187660.1:g.3379025_3379032del, NT_187660.1:g.3379027_3379032del, NT_187660.1:g.3379028_3379032del, NT_187660.1:g.3379029_3379032del, NT_187660.1:g.3379030_3379032del, NT_187660.1:g.3379031_3379032del, NT_187660.1:g.3379032del, NT_187660.1:g.3379031_3379032dup, NT_187660.1:g.3379030_3379032dup, NT_187660.1:g.3379029_3379032dup, NT_187660.1:g.3379028_3379032dup, NT_187660.1:g.3379027_3379032dup, NT_187660.1:g.3379026_3379032dup, NT_187660.1:g.3379023_3379032dup, NT_187660.1:g.3379009_3379032dup, NT_187660.1:g.3379008_3379032A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

      3.

      rs1491529309 has merged into rs57964365 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
        Chromosome:
        15:31124668 (GRCh38)
        15:31416871 (GRCh37)
        Canonical SPDI:
        NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31124654:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAA
        Gene:
        TRPM1 (Varview)
        Functional Consequence:
        genic_upstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        AAAAAAAAAAAAAAAA=0./0 (ALFA)
        -=0.4/16 (GENOME_DK)
        A=0.4305/2156 (1000Genomes)
        HGVS:
        NC_000015.10:g.31124668_31124674del, NC_000015.10:g.31124669_31124674del, NC_000015.10:g.31124671_31124674del, NC_000015.10:g.31124672_31124674del, NC_000015.10:g.31124673_31124674del, NC_000015.10:g.31124674del, NC_000015.10:g.31124674dup, NC_000015.10:g.31124673_31124674dup, NC_000015.10:g.31124672_31124674dup, NC_000015.10:g.31124669_31124674dup, NC_000015.10:g.31124667_31124674dup, NC_000015.10:g.31124674_31124675insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.31124655_31124674A[21]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000015.9:g.31416871_31416877del, NC_000015.9:g.31416872_31416877del, NC_000015.9:g.31416874_31416877del, NC_000015.9:g.31416875_31416877del, NC_000015.9:g.31416876_31416877del, NC_000015.9:g.31416877del, NC_000015.9:g.31416877dup, NC_000015.9:g.31416876_31416877dup, NC_000015.9:g.31416875_31416877dup, NC_000015.9:g.31416872_31416877dup, NC_000015.9:g.31416870_31416877dup, NC_000015.9:g.31416877_31416878insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.31416858_31416877A[21]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016453.2:g.41613_41619del, NG_016453.2:g.41614_41619del, NG_016453.2:g.41616_41619del, NG_016453.2:g.41617_41619del, NG_016453.2:g.41618_41619del, NG_016453.2:g.41619del, NG_016453.2:g.41619dup, NG_016453.2:g.41618_41619dup, NG_016453.2:g.41617_41619dup, NG_016453.2:g.41614_41619dup, NG_016453.2:g.41612_41619dup, NG_016453.2:g.41619_41620insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.41600_41619T[26]GTTTTTTTTTTTTTTTTTTTTT[1], NW_011332701.1:g.3297959_3297965del, NW_011332701.1:g.3297960_3297965del, NW_011332701.1:g.3297962_3297965del, NW_011332701.1:g.3297963_3297965del, NW_011332701.1:g.3297964_3297965del, NW_011332701.1:g.3297965del, NW_011332701.1:g.3297965dup, NW_011332701.1:g.3297964_3297965dup, NW_011332701.1:g.3297963_3297965dup, NW_011332701.1:g.3297960_3297965dup, NW_011332701.1:g.3297958_3297965dup, NW_011332701.1:g.3297965_3297966insAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_011332701.1:g.3297946_3297965A[21]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187660.1:g.3410411_3410417del, NT_187660.1:g.3410412_3410417del, NT_187660.1:g.3410414_3410417del, NT_187660.1:g.3410415_3410417del, NT_187660.1:g.3410416_3410417del, NT_187660.1:g.3410417del, NT_187660.1:g.3410417dup, NT_187660.1:g.3410416_3410417dup, NT_187660.1:g.3410415_3410417dup, NT_187660.1:g.3410412_3410417dup, NT_187660.1:g.3410410_3410417dup, NT_187660.1:g.3410417_3410418insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187660.1:g.3410398_3410417A[21]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

        4.

        rs1491523130 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          CA>- [Show Flanks]
          Chromosome:
          15:31103813 (GRCh38)
          15:31396016 (GRCh37)
          Canonical SPDI:
          NC_000015.10:31103812:CA:
          Gene:
          TRPM1 (Varview)
          Functional Consequence:
          intron_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0.0016/19 (ALFA)
          -=0.00028/16 (GnomAD)
          HGVS:

          5.

          rs1491482700 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            CA>- [Show Flanks]
            Chromosome:
            15:31124654 (GRCh38)
            15:31416857 (GRCh37)
            Canonical SPDI:
            NC_000015.10:31124653:CA:
            Gene:
            TRPM1 (Varview)
            Functional Consequence:
            intron_variant,genic_upstream_transcript_variant
            Validated:
            by frequency,by alfa
            MAF:
            -=0.00025/3 (ALFA)
            HGVS:

            6.

            rs1491482368 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              ->GG
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491451917 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                AT>- [Show Flanks]
                Chromosome:
                15:31077810 (GRCh38)
                15:31370013 (GRCh37)
                Canonical SPDI:
                NC_000015.10:31077809:AT:
                Gene:
                TRPM1 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                -=0.000214/3 (ALFA)
                -=0.000026/7 (TOPMED)
                -=0.000029/4 (GnomAD)
                HGVS:

                8.

                rs1491446587 has merged into rs3080947 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  15:31113438 (GRCh38)
                  15:31405641 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:31113432:TTTTTTTTTTTT:TTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:31113432:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
                  Gene:
                  TRPM1 (Varview)
                  Functional Consequence:
                  genic_upstream_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTT=0./0 (ALFA)
                  TTT=0.4664/1974 (1000Genomes)
                  HGVS:
                  NC_000015.10:g.31113438_31113444del, NC_000015.10:g.31113439_31113444del, NC_000015.10:g.31113441_31113444del, NC_000015.10:g.31113442_31113444del, NC_000015.10:g.31113443_31113444del, NC_000015.10:g.31113444del, NC_000015.10:g.31113444dup, NC_000015.10:g.31113443_31113444dup, NC_000015.10:g.31113442_31113444dup, NC_000015.10:g.31113441_31113444dup, NC_000015.10:g.31113440_31113444dup, NC_000015.9:g.31405641_31405647del, NC_000015.9:g.31405642_31405647del, NC_000015.9:g.31405644_31405647del, NC_000015.9:g.31405645_31405647del, NC_000015.9:g.31405646_31405647del, NC_000015.9:g.31405647del, NC_000015.9:g.31405647dup, NC_000015.9:g.31405646_31405647dup, NC_000015.9:g.31405645_31405647dup, NC_000015.9:g.31405644_31405647dup, NC_000015.9:g.31405643_31405647dup, NG_016453.2:g.52835_52841del, NG_016453.2:g.52836_52841del, NG_016453.2:g.52838_52841del, NG_016453.2:g.52839_52841del, NG_016453.2:g.52840_52841del, NG_016453.2:g.52841del, NG_016453.2:g.52841dup, NG_016453.2:g.52840_52841dup, NG_016453.2:g.52839_52841dup, NG_016453.2:g.52838_52841dup, NG_016453.2:g.52837_52841dup, NW_011332701.1:g.3286724_3286730del, NW_011332701.1:g.3286725_3286730del, NW_011332701.1:g.3286727_3286730del, NW_011332701.1:g.3286728_3286730del, NW_011332701.1:g.3286729_3286730del, NW_011332701.1:g.3286730del, NW_011332701.1:g.3286730dup, NW_011332701.1:g.3286729_3286730dup, NW_011332701.1:g.3286728_3286730dup, NW_011332701.1:g.3286727_3286730dup, NW_011332701.1:g.3286726_3286730dup, NT_187660.1:g.3399176_3399182del, NT_187660.1:g.3399177_3399182del, NT_187660.1:g.3399179_3399182del, NT_187660.1:g.3399180_3399182del, NT_187660.1:g.3399181_3399182del, NT_187660.1:g.3399182del, NT_187660.1:g.3399182dup, NT_187660.1:g.3399181_3399182dup, NT_187660.1:g.3399180_3399182dup, NT_187660.1:g.3399179_3399182dup, NT_187660.1:g.3399178_3399182dup

                  9.

                  rs1491446427 has merged into rs1178622479 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    15:31164574 (GRCh38)
                    15:31456777 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31164564:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAA=0./0 (ALFA)
                    HGVS:
                    NC_000015.10:g.31164574_31164589del, NC_000015.10:g.31164576_31164589del, NC_000015.10:g.31164577_31164589del, NC_000015.10:g.31164578_31164589del, NC_000015.10:g.31164580_31164589del, NC_000015.10:g.31164581_31164589del, NC_000015.10:g.31164585_31164589del, NC_000015.10:g.31164586_31164589del, NC_000015.10:g.31164587_31164589del, NC_000015.10:g.31164588_31164589del, NC_000015.10:g.31164589del, NC_000015.10:g.31164589dup, NC_000015.10:g.31164588_31164589dup, NC_000015.10:g.31164587_31164589dup, NC_000015.10:g.31164586_31164589dup, NC_000015.10:g.31164585_31164589dup, NC_000015.10:g.31164584_31164589dup, NC_000015.10:g.31164583_31164589dup, NC_000015.10:g.31164582_31164589dup, NC_000015.10:g.31164581_31164589dup, NC_000015.10:g.31164580_31164589dup, NC_000015.10:g.31164579_31164589dup, NC_000015.10:g.31164578_31164589dup, NC_000015.10:g.31164577_31164589dup, NC_000015.10:g.31164576_31164589dup, NC_000015.10:g.31164575_31164589dup, NC_000015.10:g.31164574_31164589dup, NC_000015.10:g.31164572_31164589dup, NC_000015.10:g.31164570_31164589dup, NC_000015.10:g.31164568_31164589dup, NC_000015.10:g.31164566_31164589dup, NC_000015.10:g.31164589_31164590insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.31164589_31164590insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.31164589_31164590insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.31164589_31164590insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.31164565_31164589A[36]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000015.9:g.31456777_31456792del, NC_000015.9:g.31456779_31456792del, NC_000015.9:g.31456780_31456792del, NC_000015.9:g.31456781_31456792del, NC_000015.9:g.31456783_31456792del, NC_000015.9:g.31456784_31456792del, NC_000015.9:g.31456788_31456792del, NC_000015.9:g.31456789_31456792del, NC_000015.9:g.31456790_31456792del, NC_000015.9:g.31456791_31456792del, NC_000015.9:g.31456792del, NC_000015.9:g.31456792dup, NC_000015.9:g.31456791_31456792dup, NC_000015.9:g.31456790_31456792dup, NC_000015.9:g.31456789_31456792dup, NC_000015.9:g.31456788_31456792dup, NC_000015.9:g.31456787_31456792dup, NC_000015.9:g.31456786_31456792dup, NC_000015.9:g.31456785_31456792dup, NC_000015.9:g.31456784_31456792dup, NC_000015.9:g.31456783_31456792dup, NC_000015.9:g.31456782_31456792dup, NC_000015.9:g.31456781_31456792dup, NC_000015.9:g.31456780_31456792dup, NC_000015.9:g.31456779_31456792dup, NC_000015.9:g.31456778_31456792dup, NC_000015.9:g.31456777_31456792dup, NC_000015.9:g.31456775_31456792dup, NC_000015.9:g.31456773_31456792dup, NC_000015.9:g.31456771_31456792dup, NC_000015.9:g.31456769_31456792dup, NC_000015.9:g.31456792_31456793insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.31456792_31456793insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.31456792_31456793insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.31456792_31456793insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.31456768_31456792A[36]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016453.2:g.1694_1709del, NG_016453.2:g.1696_1709del, NG_016453.2:g.1697_1709del, NG_016453.2:g.1698_1709del, NG_016453.2:g.1700_1709del, NG_016453.2:g.1701_1709del, NG_016453.2:g.1705_1709del, NG_016453.2:g.1706_1709del, NG_016453.2:g.1707_1709del, NG_016453.2:g.1708_1709del, NG_016453.2:g.1709del, NG_016453.2:g.1709dup, NG_016453.2:g.1708_1709dup, NG_016453.2:g.1707_1709dup, NG_016453.2:g.1706_1709dup, NG_016453.2:g.1705_1709dup, NG_016453.2:g.1704_1709dup, NG_016453.2:g.1703_1709dup, NG_016453.2:g.1702_1709dup, NG_016453.2:g.1701_1709dup, NG_016453.2:g.1700_1709dup, NG_016453.2:g.1699_1709dup, NG_016453.2:g.1698_1709dup, NG_016453.2:g.1697_1709dup, NG_016453.2:g.1696_1709dup, NG_016453.2:g.1695_1709dup, NG_016453.2:g.1694_1709dup, NG_016453.2:g.1692_1709dup, NG_016453.2:g.1690_1709dup, NG_016453.2:g.1688_1709dup, NG_016453.2:g.1686_1709dup, NG_016453.2:g.1709_1710insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.1709_1710insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.1709_1710insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.1709_1710insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.1685_1709T[39]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

                    10.

                    rs1491444182 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AC>- [Show Flanks]
                      Chromosome:
                      15:31120982 (GRCh38)
                      15:31413185 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:31120980:CAC:C
                      Gene:
                      TRPM1 (Varview)
                      Functional Consequence:
                      intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      C=0./0 (ALFA)
                      -=0.000011/3 (TOPMED)
                      HGVS:

                      11.

                      rs1491441181 has merged into rs373067641 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        TGTG>-,TG,TGTGTG [Show Flanks]
                        Chromosome:
                        15:31077821 (GRCh38)
                        15:31370024 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:31077810:TGTGTGTGTGTGTG:TGTGTGTGTG,NC_000015.10:31077810:TGTGTGTGTGTGTG:TGTGTGTGTGTG,NC_000015.10:31077810:TGTGTGTGTGTGTG:TGTGTGTGTGTGTGTG
                        Gene:
                        TRPM1 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        TGTGTGTGTGTG=0./0 (ALFA)
                        -=0.00026/1 (ALSPAC)
                        -=0.00062/4 (1000Genomes)
                        -=0.00113/31 (TOMMO)
                        HGVS:

                        12.

                        rs1491437849 [Homo sapiens]
                          Variant type:
                          SNV:
                          Alleles:
                          ->TTTTTATTTTTTTTTTTTTTTTTTT
                          Chromosome:
                          no mapping
                          Canonical SPDI:

                          13.

                          rs1491416493 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            AT>- [Show Flanks]
                            Chromosome:
                            15:31089310 (GRCh38)
                            15:31381513 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:31089308:TAT:T
                            Gene:
                            TRPM1 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            T=0./0 (ALFA)
                            -=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1491402072 [Homo sapiens]
                              Variant type:
                              INS
                              Alleles:
                              ->GACACACACATAC [Show Flanks]
                              Chromosome:
                              15:31060135 (GRCh38)
                              15:31352339 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:31060135::GACACACACATAC
                              Gene:
                              TRPM1 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant
                              HGVS:

                              15.

                              rs1491393771 has merged into rs10706621 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAAAAAAA [Show Flanks]
                                Chromosome:
                                15:31103825 (GRCh38)
                                15:31396028 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:31103813:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
                                Gene:
                                TRPM1 (Varview)
                                Functional Consequence:
                                genic_upstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                AAAAAAAAAAAA=0./0 (ALFA)
                                AA=0.000004/1 (TOPMED)
                                -=0.218993/844 (ALSPAC)
                                -=0.497005/2489 (1000Genomes)
                                HGVS:
                                NC_000015.10:g.31103825_31103828del, NC_000015.10:g.31103826_31103828del, NC_000015.10:g.31103827_31103828del, NC_000015.10:g.31103828del, NC_000015.10:g.31103828dup, NC_000015.10:g.31103827_31103828dup, NC_000015.10:g.31103821_31103828dup, NC_000015.9:g.31396028_31396031del, NC_000015.9:g.31396029_31396031del, NC_000015.9:g.31396030_31396031del, NC_000015.9:g.31396031del, NC_000015.9:g.31396031dup, NC_000015.9:g.31396030_31396031dup, NC_000015.9:g.31396024_31396031dup, NG_016453.2:g.62457_62460del, NG_016453.2:g.62458_62460del, NG_016453.2:g.62459_62460del, NG_016453.2:g.62460del, NG_016453.2:g.62460dup, NG_016453.2:g.62459_62460dup, NG_016453.2:g.62453_62460dup, NW_011332701.1:g.3277109_3277112del, NW_011332701.1:g.3277110_3277112del, NW_011332701.1:g.3277111_3277112del, NW_011332701.1:g.3277112del, NW_011332701.1:g.3277112dup, NW_011332701.1:g.3277111_3277112dup, NW_011332701.1:g.3277105_3277112dup, NT_187660.1:g.3389561_3389564del, NT_187660.1:g.3389562_3389564del, NT_187660.1:g.3389563_3389564del, NT_187660.1:g.3389564del, NT_187660.1:g.3389564dup, NT_187660.1:g.3389563_3389564dup, NT_187660.1:g.3389557_3389564dup

                                16.

                                rs1491391645 [Homo sapiens]
                                  Variant type:
                                  INS
                                  Alleles:
                                  ->AT,CT,T,TT [Show Flanks]
                                  Chromosome:
                                  15:31113431 (GRCh38)
                                  15:31405635 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:31113431::AT,NC_000015.10:31113431::CT,NC_000015.10:31113431::T,NC_000015.10:31113431::TT
                                  Gene:
                                  TRPM1 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  CT=0./0 (ALFA)
                                  HGVS:

                                  17.

                                  rs1491376292 has merged into rs59878175 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    AAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                                    Chromosome:
                                    15:31125741 (GRCh38)
                                    15:31417944 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:31125729:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                                    Gene:
                                    TRPM1 (Varview)
                                    Functional Consequence:
                                    genic_upstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    AAAAAAAAAAA=0./0 (ALFA)
                                    -=0.175/7 (GENOME_DK)
                                    HGVS:
                                    NC_000015.10:g.31125741_31125756del, NC_000015.10:g.31125742_31125756del, NC_000015.10:g.31125744_31125756del, NC_000015.10:g.31125745_31125756del, NC_000015.10:g.31125746_31125756del, NC_000015.10:g.31125747_31125756del, NC_000015.10:g.31125748_31125756del, NC_000015.10:g.31125749_31125756del, NC_000015.10:g.31125750_31125756del, NC_000015.10:g.31125751_31125756del, NC_000015.10:g.31125752_31125756del, NC_000015.10:g.31125753_31125756del, NC_000015.10:g.31125754_31125756del, NC_000015.10:g.31125755_31125756del, NC_000015.10:g.31125756del, NC_000015.10:g.31125756dup, NC_000015.10:g.31125755_31125756dup, NC_000015.10:g.31125754_31125756dup, NC_000015.10:g.31125753_31125756dup, NC_000015.10:g.31125752_31125756dup, NC_000015.10:g.31125751_31125756dup, NC_000015.10:g.31125747_31125756dup, NC_000015.9:g.31417944_31417959del, NC_000015.9:g.31417945_31417959del, NC_000015.9:g.31417947_31417959del, NC_000015.9:g.31417948_31417959del, NC_000015.9:g.31417949_31417959del, NC_000015.9:g.31417950_31417959del, NC_000015.9:g.31417951_31417959del, NC_000015.9:g.31417952_31417959del, NC_000015.9:g.31417953_31417959del, NC_000015.9:g.31417954_31417959del, NC_000015.9:g.31417955_31417959del, NC_000015.9:g.31417956_31417959del, NC_000015.9:g.31417957_31417959del, NC_000015.9:g.31417958_31417959del, NC_000015.9:g.31417959del, NC_000015.9:g.31417959dup, NC_000015.9:g.31417958_31417959dup, NC_000015.9:g.31417957_31417959dup, NC_000015.9:g.31417956_31417959dup, NC_000015.9:g.31417955_31417959dup, NC_000015.9:g.31417954_31417959dup, NC_000015.9:g.31417950_31417959dup, NG_016453.2:g.40529_40544del, NG_016453.2:g.40530_40544del, NG_016453.2:g.40532_40544del, NG_016453.2:g.40533_40544del, NG_016453.2:g.40534_40544del, NG_016453.2:g.40535_40544del, NG_016453.2:g.40536_40544del, NG_016453.2:g.40537_40544del, NG_016453.2:g.40538_40544del, NG_016453.2:g.40539_40544del, NG_016453.2:g.40540_40544del, NG_016453.2:g.40541_40544del, NG_016453.2:g.40542_40544del, NG_016453.2:g.40543_40544del, NG_016453.2:g.40544del, NG_016453.2:g.40544dup, NG_016453.2:g.40543_40544dup, NG_016453.2:g.40542_40544dup, NG_016453.2:g.40541_40544dup, NG_016453.2:g.40540_40544dup, NG_016453.2:g.40539_40544dup, NG_016453.2:g.40535_40544dup, NW_011332701.1:g.3299032_3299047del, NW_011332701.1:g.3299033_3299047del, NW_011332701.1:g.3299035_3299047del, NW_011332701.1:g.3299036_3299047del, NW_011332701.1:g.3299037_3299047del, NW_011332701.1:g.3299038_3299047del, NW_011332701.1:g.3299039_3299047del, NW_011332701.1:g.3299040_3299047del, NW_011332701.1:g.3299041_3299047del, NW_011332701.1:g.3299042_3299047del, NW_011332701.1:g.3299043_3299047del, NW_011332701.1:g.3299044_3299047del, NW_011332701.1:g.3299045_3299047del, NW_011332701.1:g.3299046_3299047del, NW_011332701.1:g.3299047del, NW_011332701.1:g.3299047dup, NW_011332701.1:g.3299046_3299047dup, NW_011332701.1:g.3299045_3299047dup, NW_011332701.1:g.3299044_3299047dup, NW_011332701.1:g.3299043_3299047dup, NW_011332701.1:g.3299042_3299047dup, NW_011332701.1:g.3299038_3299047dup, NT_187660.1:g.3411484_3411499del, NT_187660.1:g.3411485_3411499del, NT_187660.1:g.3411487_3411499del, NT_187660.1:g.3411488_3411499del, NT_187660.1:g.3411489_3411499del, NT_187660.1:g.3411490_3411499del, NT_187660.1:g.3411491_3411499del, NT_187660.1:g.3411492_3411499del, NT_187660.1:g.3411493_3411499del, NT_187660.1:g.3411494_3411499del, NT_187660.1:g.3411495_3411499del, NT_187660.1:g.3411496_3411499del, NT_187660.1:g.3411497_3411499del, NT_187660.1:g.3411498_3411499del, NT_187660.1:g.3411499del, NT_187660.1:g.3411499dup, NT_187660.1:g.3411498_3411499dup, NT_187660.1:g.3411497_3411499dup, NT_187660.1:g.3411496_3411499dup, NT_187660.1:g.3411495_3411499dup, NT_187660.1:g.3411494_3411499dup, NT_187660.1:g.3411490_3411499dup

                                    18.

                                    rs1491366479 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      GA>TCT [Show Flanks]
                                      Chromosome:
                                      15:31118893 (GRCh38)
                                      15:31411096 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:31118892:GA:TCT
                                      Gene:
                                      TRPM1 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by cluster
                                      HGVS:

                                      19.

                                      rs1491364019 has merged into rs71110846 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        TTTTTTTTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTCTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                        Chromosome:
                                        15:31165590 (GRCh38)
                                        15:31457793 (GRCh37)
                                        Canonical SPDI:
                                        NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTCTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31165579:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TTTTTTTTTTT=0./0 (ALFA)
                                        -=0.000015/4 (TOPMED)
                                        T=0.050152/33 (Korea1K)
                                        HGVS:
                                        NC_000015.10:g.31165590_31165598del, NC_000015.10:g.31165591_31165598del, NC_000015.10:g.31165592_31165598del, NC_000015.10:g.31165594_31165598del, NC_000015.10:g.31165595_31165598del, NC_000015.10:g.31165596_31165598del, NC_000015.10:g.31165597_31165598del, NC_000015.10:g.31165598del, NC_000015.10:g.31165598dup, NC_000015.10:g.31165597_31165598dup, NC_000015.10:g.31165596_31165598dup, NC_000015.10:g.31165580_31165598T[22]CT[2]T[21], NC_000015.10:g.31165595_31165598dup, NC_000015.10:g.31165594_31165598dup, NC_000015.10:g.31165580_31165598T[24]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.10:g.31165580_31165598T[24]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.10:g.31165593_31165598dup, NC_000015.10:g.31165592_31165598dup, NC_000015.10:g.31165591_31165598dup, NC_000015.10:g.31165590_31165598dup, NC_000015.10:g.31165589_31165598dup, NC_000015.10:g.31165588_31165598dup, NC_000015.10:g.31165587_31165598dup, NC_000015.10:g.31165586_31165598dup, NC_000015.10:g.31165585_31165598dup, NC_000015.10:g.31165584_31165598dup, NC_000015.10:g.31165583_31165598dup, NC_000015.10:g.31165582_31165598dup, NC_000015.10:g.31165581_31165598dup, NC_000015.10:g.31165580_31165598dup, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.31165598_31165599insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457793_31457801del, NC_000015.9:g.31457794_31457801del, NC_000015.9:g.31457795_31457801del, NC_000015.9:g.31457797_31457801del, NC_000015.9:g.31457798_31457801del, NC_000015.9:g.31457799_31457801del, NC_000015.9:g.31457800_31457801del, NC_000015.9:g.31457801del, NC_000015.9:g.31457801dup, NC_000015.9:g.31457800_31457801dup, NC_000015.9:g.31457799_31457801dup, NC_000015.9:g.31457783_31457801T[22]CT[2]T[21], NC_000015.9:g.31457798_31457801dup, NC_000015.9:g.31457797_31457801dup, NC_000015.9:g.31457783_31457801T[24]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.9:g.31457783_31457801T[24]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.9:g.31457796_31457801dup, NC_000015.9:g.31457795_31457801dup, NC_000015.9:g.31457794_31457801dup, NC_000015.9:g.31457793_31457801dup, NC_000015.9:g.31457792_31457801dup, NC_000015.9:g.31457791_31457801dup, NC_000015.9:g.31457790_31457801dup, NC_000015.9:g.31457789_31457801dup, NC_000015.9:g.31457788_31457801dup, NC_000015.9:g.31457787_31457801dup, NC_000015.9:g.31457786_31457801dup, NC_000015.9:g.31457785_31457801dup, NC_000015.9:g.31457784_31457801dup, NC_000015.9:g.31457783_31457801dup, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.31457801_31457802insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016453.2:g.686_694del, NG_016453.2:g.687_694del, NG_016453.2:g.688_694del, NG_016453.2:g.690_694del, NG_016453.2:g.691_694del, NG_016453.2:g.692_694del, NG_016453.2:g.693_694del, NG_016453.2:g.694del, NG_016453.2:g.694dup, NG_016453.2:g.693_694dup, NG_016453.2:g.692_694dup, NG_016453.2:g.676_694A[22]GA[2]A[21], NG_016453.2:g.691_694dup, NG_016453.2:g.690_694dup, NG_016453.2:g.676_694A[21]GAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016453.2:g.676_694A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016453.2:g.689_694dup, NG_016453.2:g.688_694dup, NG_016453.2:g.687_694dup, NG_016453.2:g.686_694dup, NG_016453.2:g.685_694dup, NG_016453.2:g.684_694dup, NG_016453.2:g.683_694dup, NG_016453.2:g.682_694dup, NG_016453.2:g.681_694dup, NG_016453.2:g.680_694dup, NG_016453.2:g.679_694dup, NG_016453.2:g.678_694dup, NG_016453.2:g.677_694dup, NG_016453.2:g.676_694dup, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016453.2:g.694_695insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_011332701.1:g.3338906_3338914del, NW_011332701.1:g.3338907_3338914del, NW_011332701.1:g.3338908_3338914del, NW_011332701.1:g.3338910_3338914del, NW_011332701.1:g.3338911_3338914del, NW_011332701.1:g.3338912_3338914del, NW_011332701.1:g.3338913_3338914del, NW_011332701.1:g.3338914del, NW_011332701.1:g.3338914dup, NW_011332701.1:g.3338913_3338914dup, NW_011332701.1:g.3338912_3338914dup, NW_011332701.1:g.3338894_3338914T[24]CT[2]T[21], NW_011332701.1:g.3338911_3338914dup, NW_011332701.1:g.3338910_3338914dup, NW_011332701.1:g.3338914_3338915insTTTTTCTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338894_3338914T[26]CTTTTTTTTTTTTTTTTTTTTTT[1], NW_011332701.1:g.3338909_3338914dup, NW_011332701.1:g.3338908_3338914dup, NW_011332701.1:g.3338907_3338914dup, NW_011332701.1:g.3338906_3338914dup, NW_011332701.1:g.3338905_3338914dup, NW_011332701.1:g.3338904_3338914dup, NW_011332701.1:g.3338903_3338914dup, NW_011332701.1:g.3338902_3338914dup, NW_011332701.1:g.3338901_3338914dup, NW_011332701.1:g.3338900_3338914dup, NW_011332701.1:g.3338899_3338914dup, NW_011332701.1:g.3338898_3338914dup, NW_011332701.1:g.3338897_3338914dup, NW_011332701.1:g.3338896_3338914dup, NW_011332701.1:g.3338895_3338914dup, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_011332701.1:g.3338914_3338915insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451358_3451366del, NT_187660.1:g.3451359_3451366del, NT_187660.1:g.3451360_3451366del, NT_187660.1:g.3451362_3451366del, NT_187660.1:g.3451363_3451366del, NT_187660.1:g.3451364_3451366del, NT_187660.1:g.3451365_3451366del, NT_187660.1:g.3451366del, NT_187660.1:g.3451366dup, NT_187660.1:g.3451365_3451366dup, NT_187660.1:g.3451364_3451366dup, NT_187660.1:g.3451346_3451366T[24]CT[2]T[21], NT_187660.1:g.3451363_3451366dup, NT_187660.1:g.3451362_3451366dup, NT_187660.1:g.3451366_3451367insTTTTTCTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451346_3451366T[26]CTTTTTTTTTTTTTTTTTTTTTT[1], NT_187660.1:g.3451361_3451366dup, NT_187660.1:g.3451360_3451366dup, NT_187660.1:g.3451359_3451366dup, NT_187660.1:g.3451358_3451366dup, NT_187660.1:g.3451357_3451366dup, NT_187660.1:g.3451356_3451366dup, NT_187660.1:g.3451355_3451366dup, NT_187660.1:g.3451354_3451366dup, NT_187660.1:g.3451353_3451366dup, NT_187660.1:g.3451352_3451366dup, NT_187660.1:g.3451351_3451366dup, NT_187660.1:g.3451350_3451366dup, NT_187660.1:g.3451349_3451366dup, NT_187660.1:g.3451348_3451366dup, NT_187660.1:g.3451347_3451366dup, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187660.1:g.3451366_3451367insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                                        20.

                                        rs1491363173 has merged into rs34583108 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TTTTTTTTT>-,T,TT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
                                          Chromosome:
                                          15:31144724 (GRCh38)
                                          15:31436927 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:31144712:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
                                          Gene:
                                          TRPM1 (Varview)
                                          Functional Consequence:
                                          genic_upstream_transcript_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TTTTTTTTTTTT=0./0 (ALFA)
                                          -=0.05424/32 (NorthernSweden)
                                          HGVS:
                                          NC_000015.10:g.31144724_31144732del, NC_000015.10:g.31144725_31144732del, NC_000015.10:g.31144726_31144732del, NC_000015.10:g.31144730_31144732del, NC_000015.10:g.31144731_31144732del, NC_000015.10:g.31144732del, NC_000015.10:g.31144732dup, NC_000015.10:g.31144731_31144732dup, NC_000015.10:g.31144730_31144732dup, NC_000015.10:g.31144729_31144732dup, NC_000015.9:g.31436927_31436935del, NC_000015.9:g.31436928_31436935del, NC_000015.9:g.31436929_31436935del, NC_000015.9:g.31436933_31436935del, NC_000015.9:g.31436934_31436935del, NC_000015.9:g.31436935del, NC_000015.9:g.31436935dup, NC_000015.9:g.31436934_31436935dup, NC_000015.9:g.31436933_31436935dup, NC_000015.9:g.31436932_31436935dup, NG_016453.2:g.21553_21561del, NG_016453.2:g.21554_21561del, NG_016453.2:g.21555_21561del, NG_016453.2:g.21559_21561del, NG_016453.2:g.21560_21561del, NG_016453.2:g.21561del, NG_016453.2:g.21561dup, NG_016453.2:g.21560_21561dup, NG_016453.2:g.21559_21561dup, NG_016453.2:g.21558_21561dup, NW_011332701.1:g.3318032_3318040del, NW_011332701.1:g.3318033_3318040del, NW_011332701.1:g.3318034_3318040del, NW_011332701.1:g.3318038_3318040del, NW_011332701.1:g.3318039_3318040del, NW_011332701.1:g.3318040del, NW_011332701.1:g.3318040dup, NW_011332701.1:g.3318039_3318040dup, NW_011332701.1:g.3318038_3318040dup, NW_011332701.1:g.3318037_3318040dup, NT_187660.1:g.3430484_3430492del, NT_187660.1:g.3430485_3430492del, NT_187660.1:g.3430486_3430492del, NT_187660.1:g.3430490_3430492del, NT_187660.1:g.3430491_3430492del, NT_187660.1:g.3430492del, NT_187660.1:g.3430492dup, NT_187660.1:g.3430491_3430492dup, NT_187660.1:g.3430490_3430492dup, NT_187660.1:g.3430489_3430492dup

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