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Items: 1 to 20 of 1000

1.

rs1491565309 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    TA>- [Show Flanks]
    Chromosome:
    15:41557663 (GRCh38)
    15:41849861 (GRCh37)
    Canonical SPDI:
    NC_000015.10:41557662:TA:
    Gene:
    TYRO3 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    -=0./0 (ALFA)
    HGVS:

    2.

    rs1491494395 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CA>- [Show Flanks]
      Chromosome:
      15:41576104 (GRCh38)
      15:41868302 (GRCh37)
      Canonical SPDI:
      NC_000015.10:41576103:CA:
      Gene:
      TYRO3 (Varview)
      Functional Consequence:
      3_prime_UTR_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0.00388/46 (ALFA)
      HGVS:

      3.

      rs1491490131 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        GC>- [Show Flanks]
        Chromosome:
        15:41570709 (GRCh38)
        15:41862907 (GRCh37)
        Canonical SPDI:
        NC_000015.10:41570708:GC:
        Gene:
        TYRO3 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by cluster
        MAF:
        -=0.000132/16 (ExAC)
        HGVS:

        4.

        rs1491438332 has merged into rs11363130 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AAAAAAAAAAAAA>-,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
          Chromosome:
          15:41562343 (GRCh38)
          15:41854541 (GRCh37)
          Canonical SPDI:
          NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
          Gene:
          TYRO3 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          AAAAAAAAAAA=0./0 (ALFA)
          HGVS:
          NC_000015.10:g.41562343_41562355del, NC_000015.10:g.41562345_41562355del, NC_000015.10:g.41562346_41562355del, NC_000015.10:g.41562348_41562355del, NC_000015.10:g.41562349_41562355del, NC_000015.10:g.41562350_41562355del, NC_000015.10:g.41562351_41562355del, NC_000015.10:g.41562352_41562355del, NC_000015.10:g.41562353_41562355del, NC_000015.10:g.41562354_41562355del, NC_000015.10:g.41562355del, NC_000015.10:g.41562355dup, NC_000015.10:g.41562354_41562355dup, NC_000015.10:g.41562353_41562355dup, NC_000015.10:g.41562352_41562355dup, NC_000015.10:g.41562351_41562355dup, NC_000015.10:g.41562350_41562355dup, NC_000015.10:g.41562349_41562355dup, NC_000015.10:g.41562344_41562355dup, NC_000015.10:g.41562343_41562355dup, NC_000015.10:g.41562342_41562355dup, NC_000015.10:g.41562341_41562355dup, NC_000015.9:g.41854541_41854553del, NC_000015.9:g.41854543_41854553del, NC_000015.9:g.41854544_41854553del, NC_000015.9:g.41854546_41854553del, NC_000015.9:g.41854547_41854553del, NC_000015.9:g.41854548_41854553del, NC_000015.9:g.41854549_41854553del, NC_000015.9:g.41854550_41854553del, NC_000015.9:g.41854551_41854553del, NC_000015.9:g.41854552_41854553del, NC_000015.9:g.41854553del, NC_000015.9:g.41854553dup, NC_000015.9:g.41854552_41854553dup, NC_000015.9:g.41854551_41854553dup, NC_000015.9:g.41854550_41854553dup, NC_000015.9:g.41854549_41854553dup, NC_000015.9:g.41854548_41854553dup, NC_000015.9:g.41854547_41854553dup, NC_000015.9:g.41854542_41854553dup, NC_000015.9:g.41854541_41854553dup, NC_000015.9:g.41854540_41854553dup, NC_000015.9:g.41854539_41854553dup, NG_033013.1:g.8322_8334del, NG_033013.1:g.8324_8334del, NG_033013.1:g.8325_8334del, NG_033013.1:g.8327_8334del, NG_033013.1:g.8328_8334del, NG_033013.1:g.8329_8334del, NG_033013.1:g.8330_8334del, NG_033013.1:g.8331_8334del, NG_033013.1:g.8332_8334del, NG_033013.1:g.8333_8334del, NG_033013.1:g.8334del, NG_033013.1:g.8334dup, NG_033013.1:g.8333_8334dup, NG_033013.1:g.8332_8334dup, NG_033013.1:g.8331_8334dup, NG_033013.1:g.8330_8334dup, NG_033013.1:g.8329_8334dup, NG_033013.1:g.8328_8334dup, NG_033013.1:g.8323_8334dup, NG_033013.1:g.8322_8334dup, NG_033013.1:g.8321_8334dup, NG_033013.1:g.8320_8334dup

          5.

          rs1491422107 has merged into rs150653270 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            GCGCGCGCGCGCGC>-,GC,GCGC,GCGCGC,GCGCGCGC,GCGCGCGCGC,GCGCGCGCGCGC,GCGCGCGCGCGCGCGC,GCGCGCGCGCGCGCGCGC,GCGCGCGCGCGCGCGCGCGC,GCGCGCGCGCGCGCGCGCGCGC [Show Flanks]
            Chromosome:
            15:41560433 (GRCh38)
            15:41852631 (GRCh37)
            Canonical SPDI:
            NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC,NC_000015.10:41560428:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC
            Gene:
            TYRO3 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            GCGC=0./0 (ALFA)
            -=0.05351/32 (NorthernSweden)
            HGVS:
            NC_000015.10:g.41560429GC[2], NC_000015.10:g.41560429GC[3], NC_000015.10:g.41560429GC[4], NC_000015.10:g.41560429GC[5], NC_000015.10:g.41560429GC[6], NC_000015.10:g.41560429GC[7], NC_000015.10:g.41560429GC[8], NC_000015.10:g.41560429GC[10], NC_000015.10:g.41560429GC[11], NC_000015.10:g.41560429GC[12], NC_000015.10:g.41560429GC[13], NC_000015.9:g.41852627GC[2], NC_000015.9:g.41852627GC[3], NC_000015.9:g.41852627GC[4], NC_000015.9:g.41852627GC[5], NC_000015.9:g.41852627GC[6], NC_000015.9:g.41852627GC[7], NC_000015.9:g.41852627GC[8], NC_000015.9:g.41852627GC[10], NC_000015.9:g.41852627GC[11], NC_000015.9:g.41852627GC[12], NC_000015.9:g.41852627GC[13], NG_033013.1:g.6408GC[2], NG_033013.1:g.6408GC[3], NG_033013.1:g.6408GC[4], NG_033013.1:g.6408GC[5], NG_033013.1:g.6408GC[6], NG_033013.1:g.6408GC[7], NG_033013.1:g.6408GC[8], NG_033013.1:g.6408GC[10], NG_033013.1:g.6408GC[11], NG_033013.1:g.6408GC[12], NG_033013.1:g.6408GC[13]

            6.

            rs1491217408 has merged into rs1555395684 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ATGT>-,ATGTATGT [Show Flanks]
              Chromosome:
              15:41560393 (GRCh38)
              15:41852591 (GRCh37)
              Canonical SPDI:
              NC_000015.10:41560389:TGTATGT:TGT,NC_000015.10:41560389:TGTATGT:TGTATGTATGT
              Gene:
              TYRO3 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TGTATGTATGT=0.00006/1 (ALFA)
              HGVS:

              7.

              rs1491214323 has merged into rs71104798 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                15:41565593 (GRCh38)
                15:41857791 (GRCh37)
                Canonical SPDI:
                NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:41565582:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                Gene:
                TYRO3 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTTTTTTTTT=0./0 (ALFA)
                T=0.382/1913 (1000Genomes)
                HGVS:
                NC_000015.10:g.41565593_41565599del, NC_000015.10:g.41565594_41565599del, NC_000015.10:g.41565597_41565599del, NC_000015.10:g.41565598_41565599del, NC_000015.10:g.41565599del, NC_000015.10:g.41565599dup, NC_000015.10:g.41565598_41565599dup, NC_000015.10:g.41565597_41565599dup, NC_000015.10:g.41565595_41565599dup, NC_000015.10:g.41565594_41565599dup, NC_000015.10:g.41565593_41565599dup, NC_000015.10:g.41565592_41565599dup, NC_000015.10:g.41565588_41565599dup, NC_000015.10:g.41565587_41565599dup, NC_000015.10:g.41565585_41565599dup, NC_000015.10:g.41565599_41565600insTTTTTTTTTTTTTTTTTT, NC_000015.10:g.41565599_41565600insTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41857791_41857797del, NC_000015.9:g.41857792_41857797del, NC_000015.9:g.41857795_41857797del, NC_000015.9:g.41857796_41857797del, NC_000015.9:g.41857797del, NC_000015.9:g.41857797dup, NC_000015.9:g.41857796_41857797dup, NC_000015.9:g.41857795_41857797dup, NC_000015.9:g.41857793_41857797dup, NC_000015.9:g.41857792_41857797dup, NC_000015.9:g.41857791_41857797dup, NC_000015.9:g.41857790_41857797dup, NC_000015.9:g.41857786_41857797dup, NC_000015.9:g.41857785_41857797dup, NC_000015.9:g.41857783_41857797dup, NC_000015.9:g.41857797_41857798insTTTTTTTTTTTTTTTTTT, NC_000015.9:g.41857797_41857798insTTTTTTTTTTTTTTTTTTTT, NG_033013.1:g.11572_11578del, NG_033013.1:g.11573_11578del, NG_033013.1:g.11576_11578del, NG_033013.1:g.11577_11578del, NG_033013.1:g.11578del, NG_033013.1:g.11578dup, NG_033013.1:g.11577_11578dup, NG_033013.1:g.11576_11578dup, NG_033013.1:g.11574_11578dup, NG_033013.1:g.11573_11578dup, NG_033013.1:g.11572_11578dup, NG_033013.1:g.11571_11578dup, NG_033013.1:g.11567_11578dup, NG_033013.1:g.11566_11578dup, NG_033013.1:g.11564_11578dup, NG_033013.1:g.11578_11579insTTTTTTTTTTTTTTTTTT, NG_033013.1:g.11578_11579insTTTTTTTTTTTTTTTTTTTT

                8.

                rs1491197576 has merged into rs1177291795 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  GT>-,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTTTGTGTGTGTGT,GTTTGTGTGTGTGTGTGTGT,GTTTGTGTGTGTGTGTGTGTGT [Show Flanks]
                  Chromosome:
                  15:41560391 (GRCh38)
                  15:41852589 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:41560388:GTGT:GT,NC_000015.10:41560388:GTGT:GTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTTTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTTTGTGTGTGTGTGTGTGT,NC_000015.10:41560388:GTGT:GTGTTTGTGTGTGTGTGTGTGTGT
                  Gene:
                  TYRO3 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  GTGTGT=0./0 (ALFA)
                  GTGTGTGTGTGTGT=0.00012/2 (TOMMO)
                  HGVS:
                  NC_000015.10:g.41560389GT[1], NC_000015.10:g.41560389GT[3], NC_000015.10:g.41560389GT[4], NC_000015.10:g.41560389GT[5], NC_000015.10:g.41560389GT[6], NC_000015.10:g.41560389GT[7], NC_000015.10:g.41560389GT[8], NC_000015.10:g.41560389GT[9], NC_000015.10:g.41560389GT[10], NC_000015.10:g.41560389GT[11], NC_000015.10:g.41560389GT[12], NC_000015.10:g.41560389GT[13], NC_000015.10:g.41560389_41560392GT[2]TTGTGTGTGTGT[1], NC_000015.10:g.41560389_41560392GT[2]TTGTGTGTGTGTGTGTGT[1], NC_000015.10:g.41560389_41560392GT[2]TTGTGTGTGTGTGTGTGTGT[1], NC_000015.9:g.41852587GT[1], NC_000015.9:g.41852587GT[3], NC_000015.9:g.41852587GT[4], NC_000015.9:g.41852587GT[5], NC_000015.9:g.41852587GT[6], NC_000015.9:g.41852587GT[7], NC_000015.9:g.41852587GT[8], NC_000015.9:g.41852587GT[9], NC_000015.9:g.41852587GT[10], NC_000015.9:g.41852587GT[11], NC_000015.9:g.41852587GT[12], NC_000015.9:g.41852587GT[13], NC_000015.9:g.41852587_41852590GT[2]TTGTGTGTGTGT[1], NC_000015.9:g.41852587_41852590GT[2]TTGTGTGTGTGTGTGTGT[1], NC_000015.9:g.41852587_41852590GT[2]TTGTGTGTGTGTGTGTGTGT[1], NG_033013.1:g.6368GT[1], NG_033013.1:g.6368GT[3], NG_033013.1:g.6368GT[4], NG_033013.1:g.6368GT[5], NG_033013.1:g.6368GT[6], NG_033013.1:g.6368GT[7], NG_033013.1:g.6368GT[8], NG_033013.1:g.6368GT[9], NG_033013.1:g.6368GT[10], NG_033013.1:g.6368GT[11], NG_033013.1:g.6368GT[12], NG_033013.1:g.6368GT[13], NG_033013.1:g.6368_6371GT[2]TTGTGTGTGTGT[1], NG_033013.1:g.6368_6371GT[2]TTGTGTGTGTGTGTGTGT[1], NG_033013.1:g.6368_6371GT[2]TTGTGTGTGTGTGTGTGTGT[1]

                  9.

                  rs1491145805 has merged into rs397853986 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    15:41576120 (GRCh38)
                    15:41868318 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41576104:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    TYRO3 (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant,intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAAAAAAAAA=0./0 (ALFA)
                    -=0.4285/2146 (1000Genomes)
                    HGVS:
                    NC_000015.10:g.41576120_41576125del, NC_000015.10:g.41576121_41576125del, NC_000015.10:g.41576122_41576125del, NC_000015.10:g.41576123_41576125del, NC_000015.10:g.41576124_41576125del, NC_000015.10:g.41576125del, NC_000015.10:g.41576125dup, NC_000015.10:g.41576124_41576125dup, NC_000015.10:g.41576123_41576125dup, NC_000015.10:g.41576121_41576125dup, NC_000015.10:g.41576120_41576125dup, NC_000015.9:g.41868318_41868323del, NC_000015.9:g.41868319_41868323del, NC_000015.9:g.41868320_41868323del, NC_000015.9:g.41868321_41868323del, NC_000015.9:g.41868322_41868323del, NC_000015.9:g.41868323del, NC_000015.9:g.41868323dup, NC_000015.9:g.41868322_41868323dup, NC_000015.9:g.41868321_41868323dup, NC_000015.9:g.41868319_41868323dup, NC_000015.9:g.41868318_41868323dup, NG_033013.1:g.22099_22104del, NG_033013.1:g.22100_22104del, NG_033013.1:g.22101_22104del, NG_033013.1:g.22102_22104del, NG_033013.1:g.22103_22104del, NG_033013.1:g.22104del, NG_033013.1:g.22104dup, NG_033013.1:g.22103_22104dup, NG_033013.1:g.22102_22104dup, NG_033013.1:g.22100_22104dup, NG_033013.1:g.22099_22104dup, XM_017022543.3:c.*1889_*1894del, XM_017022543.3:c.*1890_*1894del, XM_017022543.3:c.*1891_*1894del, XM_017022543.3:c.*1892_*1894del, XM_017022543.3:c.*1893_*1894del, XM_017022543.3:c.*1894del, XM_017022543.3:c.*1894dup, XM_017022543.3:c.*1893_*1894dup, XM_017022543.3:c.*1892_*1894dup, XM_017022543.3:c.*1890_*1894dup, XM_017022543.3:c.*1889_*1894dup, XM_017022543.2:c.*1889_*1894del, XM_017022543.2:c.*1890_*1894del, XM_017022543.2:c.*1891_*1894del, XM_017022543.2:c.*1892_*1894del, XM_017022543.2:c.*1893_*1894del, XM_017022543.2:c.*1894del, XM_017022543.2:c.*1894dup, XM_017022543.2:c.*1893_*1894dup, XM_017022543.2:c.*1892_*1894dup, XM_017022543.2:c.*1890_*1894dup, XM_017022543.2:c.*1889_*1894dup

                    10.

                    rs1491123072 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      ->C [Show Flanks]
                      Chromosome:
                      15:41569315 (GRCh38)
                      15:41861514 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:41569315:C:CC
                      Gene:
                      TYRO3 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      CC=0./0 (ALFA)
                      HGVS:

                      11.

                      rs1491115560 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        CA>- [Show Flanks]
                        Chromosome:
                        15:41569316 (GRCh38)
                        15:41861514 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:41569314:ACA:A
                        Gene:
                        TYRO3 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        -=0.000004/1 (TOPMED)
                        HGVS:

                        12.

                        rs1490567817 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          T>- [Show Flanks]
                          Chromosome:
                          15:41569296 (GRCh38)
                          15:41861494 (GRCh37)
                          Canonical SPDI:
                          NC_000015.10:41569295:TT:T
                          Gene:
                          TYRO3 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          TT=0./0 (ALFA)
                          -=0.000009/1 (GnomAD)
                          HGVS:

                          13.

                          rs1490421699 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            15:41578605 (GRCh38)
                            15:41870803 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:41578604:G:A
                            Gene:
                            TYRO3 (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,genic_downstream_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1490317681 has merged into rs11363130 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              AAAAAAAAAAAAA>-,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                              Chromosome:
                              15:41562343 (GRCh38)
                              15:41854541 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:41562331:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                              Gene:
                              TYRO3 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              AAAAAAAAAAA=0./0 (ALFA)
                              HGVS:
                              NC_000015.10:g.41562343_41562355del, NC_000015.10:g.41562345_41562355del, NC_000015.10:g.41562346_41562355del, NC_000015.10:g.41562348_41562355del, NC_000015.10:g.41562349_41562355del, NC_000015.10:g.41562350_41562355del, NC_000015.10:g.41562351_41562355del, NC_000015.10:g.41562352_41562355del, NC_000015.10:g.41562353_41562355del, NC_000015.10:g.41562354_41562355del, NC_000015.10:g.41562355del, NC_000015.10:g.41562355dup, NC_000015.10:g.41562354_41562355dup, NC_000015.10:g.41562353_41562355dup, NC_000015.10:g.41562352_41562355dup, NC_000015.10:g.41562351_41562355dup, NC_000015.10:g.41562350_41562355dup, NC_000015.10:g.41562349_41562355dup, NC_000015.10:g.41562344_41562355dup, NC_000015.10:g.41562343_41562355dup, NC_000015.10:g.41562342_41562355dup, NC_000015.10:g.41562341_41562355dup, NC_000015.9:g.41854541_41854553del, NC_000015.9:g.41854543_41854553del, NC_000015.9:g.41854544_41854553del, NC_000015.9:g.41854546_41854553del, NC_000015.9:g.41854547_41854553del, NC_000015.9:g.41854548_41854553del, NC_000015.9:g.41854549_41854553del, NC_000015.9:g.41854550_41854553del, NC_000015.9:g.41854551_41854553del, NC_000015.9:g.41854552_41854553del, NC_000015.9:g.41854553del, NC_000015.9:g.41854553dup, NC_000015.9:g.41854552_41854553dup, NC_000015.9:g.41854551_41854553dup, NC_000015.9:g.41854550_41854553dup, NC_000015.9:g.41854549_41854553dup, NC_000015.9:g.41854548_41854553dup, NC_000015.9:g.41854547_41854553dup, NC_000015.9:g.41854542_41854553dup, NC_000015.9:g.41854541_41854553dup, NC_000015.9:g.41854540_41854553dup, NC_000015.9:g.41854539_41854553dup, NG_033013.1:g.8322_8334del, NG_033013.1:g.8324_8334del, NG_033013.1:g.8325_8334del, NG_033013.1:g.8327_8334del, NG_033013.1:g.8328_8334del, NG_033013.1:g.8329_8334del, NG_033013.1:g.8330_8334del, NG_033013.1:g.8331_8334del, NG_033013.1:g.8332_8334del, NG_033013.1:g.8333_8334del, NG_033013.1:g.8334del, NG_033013.1:g.8334dup, NG_033013.1:g.8333_8334dup, NG_033013.1:g.8332_8334dup, NG_033013.1:g.8331_8334dup, NG_033013.1:g.8330_8334dup, NG_033013.1:g.8329_8334dup, NG_033013.1:g.8328_8334dup, NG_033013.1:g.8323_8334dup, NG_033013.1:g.8322_8334dup, NG_033013.1:g.8321_8334dup, NG_033013.1:g.8320_8334dup

                              15.

                              rs1490256951 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                15:41579035 (GRCh38)
                                15:41871233 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:41579034:C:T
                                Gene:
                                TYRO3 (Varview)
                                Functional Consequence:
                                3_prime_UTR_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0.000071/1 (ALFA)
                                T=0.000004/1 (TOPMED)
                                HGVS:

                                16.

                                rs1490170549 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  15:41568871 (GRCh38)
                                  15:41861069 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:41568870:G:A
                                  Gene:
                                  TYRO3 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  A=0.000004/1 (GnomAD_exomes)
                                  HGVS:

                                  17.

                                  rs1490055083 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    15:41565136 (GRCh38)
                                    15:41857334 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:41565135:G:T
                                    Gene:
                                    TYRO3 (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant
                                    HGVS:

                                    18.

                                    rs1489708609 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      15:41569704 (GRCh38)
                                      15:41861902 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:41569703:C:G
                                      Gene:
                                      TYRO3 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000007/1 (GnomAD)
                                      G=0.000011/3 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1489549152 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        ->C [Show Flanks]
                                        Chromosome:
                                        15:41575550 (GRCh38)
                                        15:41867749 (GRCh37)
                                        Canonical SPDI:
                                        NC_000015.10:41575550:CCC:CCCC
                                        Gene:
                                        TYRO3 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        CCCC=0./0 (ALFA)
                                        C=0.000014/2 (GnomAD)
                                        C=0.000015/4 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1489248093 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>A [Show Flanks]
                                          Chromosome:
                                          15:41572499 (GRCh38)
                                          15:41864697 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:41572498:C:A
                                          Gene:
                                          TYRO3 (Varview)
                                          Functional Consequence:
                                          missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0.000056/2 (ALFA)
                                          A=0.000004/1 (GnomAD_exomes)
                                          A=0.000007/1 (GnomAD)
                                          A=0.000008/2 (TOPMED)
                                          HGVS:

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