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1.

rs1491583608 [Homo sapiens]
    Variant type:
    SNV:
    Alleles:
    ->CTT
    Chromosome:
    no mapping
    Canonical SPDI:

    2.

    rs1491572406 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CA>- [Show Flanks]
      Chromosome:
      12:64669890 (GRCh38)
      12:65063670 (GRCh37)
      Canonical SPDI:
      NC_000012.12:64669889:CA:
      Gene:
      RASSF3 (Varview)
      Functional Consequence:
      5_prime_UTR_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      -=0.00717/85 (ALFA)
      -=0.00067/52 (GnomAD)
      HGVS:

      3.

      rs1491548342 has merged into rs1254557437 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        CTCCCTCCCTCCCTCCCTCC>-,CTCC,CTCCCTCC,CTCCCTCCCTCC,CTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,CTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC [Show Flanks]
        Chromosome:
        12:64696103 (GRCh38)
        12:65089883 (GRCh37)
        Canonical SPDI:
        NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC,NC_000012.12:64696085:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC:CCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCC
        Gene:
        RASSF3 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        CCTCCCTCCCTCCCTCCCTCC=0./0 (ALFA)
        HGVS:
        NC_000012.12:g.64696087CTCC[4], NC_000012.12:g.64696087CTCC[5], NC_000012.12:g.64696087CTCC[6], NC_000012.12:g.64696087CTCC[7], NC_000012.12:g.64696087CTCC[8], NC_000012.12:g.64696087CTCC[10], NC_000012.12:g.64696087CTCC[11], NC_000012.12:g.64696087CTCC[12], NC_000012.12:g.64696087CTCC[13], NC_000012.12:g.64696087CTCC[14], NC_000012.12:g.64696087CTCC[15], NC_000012.11:g.65089867CTCC[4], NC_000012.11:g.65089867CTCC[5], NC_000012.11:g.65089867CTCC[6], NC_000012.11:g.65089867CTCC[7], NC_000012.11:g.65089867CTCC[8], NC_000012.11:g.65089867CTCC[10], NC_000012.11:g.65089867CTCC[11], NC_000012.11:g.65089867CTCC[12], NC_000012.11:g.65089867CTCC[13], NC_000012.11:g.65089867CTCC[14], NC_000012.11:g.65089867CTCC[15], NM_178169.4:c.*1175CTCC[4], NM_178169.4:c.*1175CTCC[5], NM_178169.4:c.*1175CTCC[6], NM_178169.4:c.*1175CTCC[7], NM_178169.4:c.*1175CTCC[8], NM_178169.4:c.*1175CTCC[10], NM_178169.4:c.*1175CTCC[11], NM_178169.4:c.*1175CTCC[12], NM_178169.4:c.*1175CTCC[13], NM_178169.4:c.*1175CTCC[14], NM_178169.4:c.*1175CTCC[15], NM_178169.3:c.*1175CTCC[4], NM_178169.3:c.*1175CTCC[5], NM_178169.3:c.*1175CTCC[6], NM_178169.3:c.*1175CTCC[7], NM_178169.3:c.*1175CTCC[8], NM_178169.3:c.*1175CTCC[10], NM_178169.3:c.*1175CTCC[11], NM_178169.3:c.*1175CTCC[12], NM_178169.3:c.*1175CTCC[13], NM_178169.3:c.*1175CTCC[14], NM_178169.3:c.*1175CTCC[15], XM_011538195.3:c.*1175CTCC[4], XM_011538195.3:c.*1175CTCC[5], XM_011538195.3:c.*1175CTCC[6], XM_011538195.3:c.*1175CTCC[7], XM_011538195.3:c.*1175CTCC[8], XM_011538195.3:c.*1175CTCC[10], XM_011538195.3:c.*1175CTCC[11], XM_011538195.3:c.*1175CTCC[12], XM_011538195.3:c.*1175CTCC[13], XM_011538195.3:c.*1175CTCC[14], XM_011538195.3:c.*1175CTCC[15], XM_011538195.2:c.*1175CTCC[4], XM_011538195.2:c.*1175CTCC[5], XM_011538195.2:c.*1175CTCC[6], XM_011538195.2:c.*1175CTCC[7], XM_011538195.2:c.*1175CTCC[8], XM_011538195.2:c.*1175CTCC[10], XM_011538195.2:c.*1175CTCC[11], XM_011538195.2:c.*1175CTCC[12], XM_011538195.2:c.*1175CTCC[13], XM_011538195.2:c.*1175CTCC[14], XM_011538195.2:c.*1175CTCC[15], XM_017019182.2:c.*1175CTCC[4], XM_017019182.2:c.*1175CTCC[5], XM_017019182.2:c.*1175CTCC[6], XM_017019182.2:c.*1175CTCC[7], XM_017019182.2:c.*1175CTCC[8], XM_017019182.2:c.*1175CTCC[10], XM_017019182.2:c.*1175CTCC[11], XM_017019182.2:c.*1175CTCC[12], XM_017019182.2:c.*1175CTCC[13], XM_017019182.2:c.*1175CTCC[14], XM_017019182.2:c.*1175CTCC[15], XM_017019182.1:c.*1175CTCC[4], XM_017019182.1:c.*1175CTCC[5], XM_017019182.1:c.*1175CTCC[6], XM_017019182.1:c.*1175CTCC[7], XM_017019182.1:c.*1175CTCC[8], XM_017019182.1:c.*1175CTCC[10], XM_017019182.1:c.*1175CTCC[11], XM_017019182.1:c.*1175CTCC[12], XM_017019182.1:c.*1175CTCC[13], XM_017019182.1:c.*1175CTCC[14], XM_017019182.1:c.*1175CTCC[15], NR_040718.2:n.1792CTCC[4], NR_040718.2:n.1792CTCC[5], NR_040718.2:n.1792CTCC[6], NR_040718.2:n.1792CTCC[7], NR_040718.2:n.1792CTCC[8], NR_040718.2:n.1792CTCC[10], NR_040718.2:n.1792CTCC[11], NR_040718.2:n.1792CTCC[12], NR_040718.2:n.1792CTCC[13], NR_040718.2:n.1792CTCC[14], NR_040718.2:n.1792CTCC[15], NR_040718.1:n.1774CTCC[4], NR_040718.1:n.1774CTCC[5], NR_040718.1:n.1774CTCC[6], NR_040718.1:n.1774CTCC[7], NR_040718.1:n.1774CTCC[8], NR_040718.1:n.1774CTCC[10], NR_040718.1:n.1774CTCC[11], NR_040718.1:n.1774CTCC[12], NR_040718.1:n.1774CTCC[13], NR_040718.1:n.1774CTCC[14], NR_040718.1:n.1774CTCC[15], XM_047428711.1:c.*1175CTCC[4], XM_047428711.1:c.*1175CTCC[5], XM_047428711.1:c.*1175CTCC[6], XM_047428711.1:c.*1175CTCC[7], XM_047428711.1:c.*1175CTCC[8], XM_047428711.1:c.*1175CTCC[10], XM_047428711.1:c.*1175CTCC[11], XM_047428711.1:c.*1175CTCC[12], XM_047428711.1:c.*1175CTCC[13], XM_047428711.1:c.*1175CTCC[14], XM_047428711.1:c.*1175CTCC[15], NM_001242691.1:c.*1381CTCC[4], NM_001242691.1:c.*1381CTCC[5], NM_001242691.1:c.*1381CTCC[6], NM_001242691.1:c.*1381CTCC[7], NM_001242691.1:c.*1381CTCC[8], NM_001242691.1:c.*1381CTCC[10], NM_001242691.1:c.*1381CTCC[11], NM_001242691.1:c.*1381CTCC[12], NM_001242691.1:c.*1381CTCC[13], NM_001242691.1:c.*1381CTCC[14], NM_001242691.1:c.*1381CTCC[15]

        4.

        rs1491528176 [Homo sapiens]
          Variant type:
          SNV:
          Alleles:
          TG>-
          Chromosome:
          no mapping
          Canonical SPDI:

          5.

          rs1491488736 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->C [Show Flanks]
            Chromosome:
            12:64641638 (GRCh38)
            12:65035419 (GRCh37)
            Canonical SPDI:
            NC_000012.12:64641638::C
            Gene:
            RASSF3 (Varview)
            Functional Consequence:
            genic_upstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            C=0./0 (ALFA)
            C=0.00004/1 (TOMMO)
            HGVS:

            6.

            rs1491474651 has merged into rs772275438 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
              Chromosome:
              12:64641650 (GRCh38)
              12:65035430 (GRCh37)
              Canonical SPDI:
              NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
              Gene:
              RASSF3 (Varview)
              Functional Consequence:
              intron_variant,genic_upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTTTTTTT=0./0 (ALFA)
              -=0.000004/1 (TOPMED)
              -=0.056995/22 (NorthernSweden)
              -=0.125/5 (GENOME_DK)
              HGVS:

              7.

              rs1491463630 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->CGGGGG [Show Flanks]
                Chromosome:
                12:64654658 (GRCh38)
                12:65048439 (GRCh37)
                Canonical SPDI:
                NC_000012.12:64654658:GGGGG:GGGGGCGGGGG
                Gene:
                RASSF3 (Varview)
                Functional Consequence:
                genic_upstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                GGGGGCGGGGG=0.00008/1 (ALFA)
                GGGGGC=0.00018/2 (TOMMO)
                HGVS:

                8.

                rs1491462428 has merged into rs71092993 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  12:64661683 (GRCh38)
                  12:65055463 (GRCh37)
                  Canonical SPDI:
                  NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64661677:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  RASSF3 (Varview)
                  Functional Consequence:
                  intron_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTT=0./0 (ALFA)
                  HGVS:
                  NC_000012.12:g.64661683_64661700del, NC_000012.12:g.64661686_64661700del, NC_000012.12:g.64661687_64661700del, NC_000012.12:g.64661688_64661700del, NC_000012.12:g.64661689_64661700del, NC_000012.12:g.64661690_64661700del, NC_000012.12:g.64661691_64661700del, NC_000012.12:g.64661692_64661700del, NC_000012.12:g.64661693_64661700del, NC_000012.12:g.64661694_64661700del, NC_000012.12:g.64661696_64661700del, NC_000012.12:g.64661697_64661700del, NC_000012.12:g.64661698_64661700del, NC_000012.12:g.64661699_64661700del, NC_000012.12:g.64661700del, NC_000012.12:g.64661700dup, NC_000012.12:g.64661699_64661700dup, NC_000012.12:g.64661698_64661700dup, NC_000012.12:g.64661697_64661700dup, NC_000012.12:g.64661696_64661700dup, NC_000012.12:g.64661695_64661700dup, NC_000012.12:g.64661694_64661700dup, NC_000012.12:g.64661693_64661700dup, NC_000012.12:g.64661692_64661700dup, NC_000012.12:g.64661691_64661700dup, NC_000012.12:g.64661690_64661700dup, NC_000012.12:g.64661689_64661700dup, NC_000012.12:g.64661688_64661700dup, NC_000012.12:g.64661687_64661700dup, NC_000012.12:g.64661686_64661700dup, NC_000012.12:g.64661684_64661700dup, NC_000012.12:g.64661700_64661701insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000012.11:g.65055463_65055480del, NC_000012.11:g.65055466_65055480del, NC_000012.11:g.65055467_65055480del, NC_000012.11:g.65055468_65055480del, NC_000012.11:g.65055469_65055480del, NC_000012.11:g.65055470_65055480del, NC_000012.11:g.65055471_65055480del, NC_000012.11:g.65055472_65055480del, NC_000012.11:g.65055473_65055480del, NC_000012.11:g.65055474_65055480del, NC_000012.11:g.65055476_65055480del, NC_000012.11:g.65055477_65055480del, NC_000012.11:g.65055478_65055480del, NC_000012.11:g.65055479_65055480del, NC_000012.11:g.65055480del, NC_000012.11:g.65055480dup, NC_000012.11:g.65055479_65055480dup, NC_000012.11:g.65055478_65055480dup, NC_000012.11:g.65055477_65055480dup, NC_000012.11:g.65055476_65055480dup, NC_000012.11:g.65055475_65055480dup, NC_000012.11:g.65055474_65055480dup, NC_000012.11:g.65055473_65055480dup, NC_000012.11:g.65055472_65055480dup, NC_000012.11:g.65055471_65055480dup, NC_000012.11:g.65055470_65055480dup, NC_000012.11:g.65055469_65055480dup, NC_000012.11:g.65055468_65055480dup, NC_000012.11:g.65055467_65055480dup, NC_000012.11:g.65055466_65055480dup, NC_000012.11:g.65055464_65055480dup, NC_000012.11:g.65055480_65055481insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                  9.

                  rs1491450770 has merged into rs138010191 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    CGCGCG>-,CG,CGCG,CGCGCGCG,CGCGCGCGCG,CGCGCGCGCGCG,CGCGCGCGCGCGCGCGCGCG [Show Flanks]
                    Chromosome:
                    12:64641423 (GRCh38)
                    12:65035203 (GRCh37)
                    Canonical SPDI:
                    NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCGCGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCGCGCGCGCGCG,NC_000012.12:64641414:CGCGCGCGCGCGCG:CGCGCGCGCGCGCGCGCGCGCGCGCGCG
                    Gene:
                    RASSF3 (Varview)
                    Functional Consequence:
                    intron_variant,genic_upstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    CGCGCGCGCG=0./0 (ALFA)
                    -=0.000008/2 (TOPMED)
                    CG=0.000071/1 (TOMMO)
                    CG=0.000461/2 (Estonian)
                    HGVS:

                    10.

                    rs1491436601 has merged into rs199913401 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      GGGGG>-,G,GG,GGG,GGGG,GGGGGG,GGGGGGG [Show Flanks]
                      Chromosome:
                      12:64654659 (GRCh38)
                      12:65048439 (GRCh37)
                      Canonical SPDI:
                      NC_000012.12:64654657:GGGGGG:G,NC_000012.12:64654657:GGGGGG:GG,NC_000012.12:64654657:GGGGGG:GGG,NC_000012.12:64654657:GGGGGG:GGGG,NC_000012.12:64654657:GGGGGG:GGGGG,NC_000012.12:64654657:GGGGGG:GGGGGGG,NC_000012.12:64654657:GGGGGG:GGGGGGGG
                      Gene:
                      RASSF3 (Varview)
                      Functional Consequence:
                      intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      GGG=0./0 (ALFA)
                      HGVS:

                      11.

                      rs1491407895 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->TA [Show Flanks]
                        Chromosome:
                        12:64641403 (GRCh38)
                        12:65035184 (GRCh37)
                        Canonical SPDI:
                        NC_000012.12:64641403:A:ATA
                        Gene:
                        RASSF3 (Varview)
                        Functional Consequence:
                        genic_upstream_transcript_variant,intron_variant
                        HGVS:

                        12.

                        rs1491393091 has merged into rs34700817 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          AAAAAA>-,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                          Chromosome:
                          12:64629972 (GRCh38)
                          12:65023752 (GRCh37)
                          Canonical SPDI:
                          NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000012.12:64629961:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                          Gene:
                          RASSF3 (Varview)
                          Functional Consequence:
                          intron_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          AAAAAAAAAAAAA=0./0 (ALFA)
                          HGVS:
                          NC_000012.12:g.64629972_64629977del, NC_000012.12:g.64629975_64629977del, NC_000012.12:g.64629976_64629977del, NC_000012.12:g.64629977del, NC_000012.12:g.64629977dup, NC_000012.12:g.64629976_64629977dup, NC_000012.12:g.64629975_64629977dup, NC_000012.12:g.64629974_64629977dup, NC_000012.12:g.64629973_64629977dup, NC_000012.12:g.64629972_64629977dup, NC_000012.12:g.64629971_64629977dup, NC_000012.12:g.64629970_64629977dup, NC_000012.12:g.64629969_64629977dup, NC_000012.12:g.64629968_64629977dup, NC_000012.12:g.64629967_64629977dup, NC_000012.12:g.64629966_64629977dup, NC_000012.12:g.64629965_64629977dup, NC_000012.12:g.64629964_64629977dup, NC_000012.12:g.64629963_64629977dup, NC_000012.12:g.64629962_64629977dup, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.12:g.64629977_64629978insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023752_65023757del, NC_000012.11:g.65023755_65023757del, NC_000012.11:g.65023756_65023757del, NC_000012.11:g.65023757del, NC_000012.11:g.65023757dup, NC_000012.11:g.65023756_65023757dup, NC_000012.11:g.65023755_65023757dup, NC_000012.11:g.65023754_65023757dup, NC_000012.11:g.65023753_65023757dup, NC_000012.11:g.65023752_65023757dup, NC_000012.11:g.65023751_65023757dup, NC_000012.11:g.65023750_65023757dup, NC_000012.11:g.65023749_65023757dup, NC_000012.11:g.65023748_65023757dup, NC_000012.11:g.65023747_65023757dup, NC_000012.11:g.65023746_65023757dup, NC_000012.11:g.65023745_65023757dup, NC_000012.11:g.65023744_65023757dup, NC_000012.11:g.65023743_65023757dup, NC_000012.11:g.65023742_65023757dup, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000012.11:g.65023757_65023758insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                          13.

                          rs1491392052 [Homo sapiens]
                            Variant type:
                            SNV:
                            Alleles:
                            ->TTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT
                            Chromosome:
                            no mapping
                            Canonical SPDI:

                            14.

                            rs1491387420 has merged into rs139897110 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TTTTTTTTTT>-,T,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                              Chromosome:
                              12:64634974 (GRCh38)
                              12:65028754 (GRCh37)
                              Canonical SPDI:
                              NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64634967:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                              Gene:
                              RASSF3 (Varview)
                              Functional Consequence:
                              intron_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TTTTTT=0./0 (ALFA)
                              -=0.000004/1 (TOPMED)
                              T=0.494209/2475 (1000Genomes)
                              HGVS:
                              NC_000012.12:g.64634974_64634983del, NC_000012.12:g.64634975_64634983del, NC_000012.12:g.64634978_64634983del, NC_000012.12:g.64634980_64634983del, NC_000012.12:g.64634981_64634983del, NC_000012.12:g.64634982_64634983del, NC_000012.12:g.64634983del, NC_000012.12:g.64634983dup, NC_000012.12:g.64634982_64634983dup, NC_000012.12:g.64634980_64634983dup, NC_000012.12:g.64634979_64634983dup, NC_000012.12:g.64634978_64634983dup, NC_000012.12:g.64634976_64634983dup, NC_000012.12:g.64634975_64634983dup, NC_000012.12:g.64634974_64634983dup, NC_000012.12:g.64634973_64634983dup, NC_000012.12:g.64634983_64634984insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000012.11:g.65028754_65028763del, NC_000012.11:g.65028755_65028763del, NC_000012.11:g.65028758_65028763del, NC_000012.11:g.65028760_65028763del, NC_000012.11:g.65028761_65028763del, NC_000012.11:g.65028762_65028763del, NC_000012.11:g.65028763del, NC_000012.11:g.65028763dup, NC_000012.11:g.65028762_65028763dup, NC_000012.11:g.65028760_65028763dup, NC_000012.11:g.65028759_65028763dup, NC_000012.11:g.65028758_65028763dup, NC_000012.11:g.65028756_65028763dup, NC_000012.11:g.65028755_65028763dup, NC_000012.11:g.65028754_65028763dup, NC_000012.11:g.65028753_65028763dup, NC_000012.11:g.65028763_65028764insTTTTTTTTTTTTTTTTTTTTTTTT

                              15.

                              rs1491382204 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ->GC,TC [Show Flanks]
                                Chromosome:
                                12:64675046 (GRCh38)
                                12:65068827 (GRCh37)
                                Canonical SPDI:
                                NC_000012.12:64675046:C:CGC,NC_000012.12:64675046:C:CTC
                                Gene:
                                RASSF3 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                CGC=0./0 (ALFA)
                                HGVS:

                                16.

                                rs1491370189 has merged into rs1555213814 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  AC>-,ACAC,ACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC [Show Flanks]
                                  Chromosome:
                                  12:64641414 (GRCh38)
                                  12:65035194 (GRCh37)
                                  Canonical SPDI:
                                  NC_000012.12:64641402:CACACACACACAC:CACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000012.12:64641402:CACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC
                                  Gene:
                                  RASSF3 (Varview)
                                  Functional Consequence:
                                  genic_upstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  CACACACACACACAC=0./0 (ALFA)
                                  CA=0.00109/2 (Korea1K)
                                  HGVS:

                                  17.

                                  rs1491351380 has merged into rs34897392 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
                                    Chromosome:
                                    12:64670556 (GRCh38)
                                    12:65064336 (GRCh37)
                                    Canonical SPDI:
                                    NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:64670544:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
                                    Gene:
                                    RASSF3 (Varview)
                                    Functional Consequence:
                                    5_prime_UTR_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    TTTTTTTTTTTTTTTTTTTTT=0./0 (ALFA)
                                    -=0.344/1723 (1000Genomes)
                                    HGVS:
                                    NC_000012.12:g.64670556_64670561del, NC_000012.12:g.64670557_64670561del, NC_000012.12:g.64670558_64670561del, NC_000012.12:g.64670559_64670561del, NC_000012.12:g.64670560_64670561del, NC_000012.12:g.64670561del, NC_000012.12:g.64670561dup, NC_000012.12:g.64670560_64670561dup, NC_000012.12:g.64670559_64670561dup, NC_000012.12:g.64670558_64670561dup, NC_000012.12:g.64670557_64670561dup, NC_000012.12:g.64670555_64670561dup, NC_000012.11:g.65064336_65064341del, NC_000012.11:g.65064337_65064341del, NC_000012.11:g.65064338_65064341del, NC_000012.11:g.65064339_65064341del, NC_000012.11:g.65064340_65064341del, NC_000012.11:g.65064341del, NC_000012.11:g.65064341dup, NC_000012.11:g.65064340_65064341dup, NC_000012.11:g.65064339_65064341dup, NC_000012.11:g.65064338_65064341dup, NC_000012.11:g.65064337_65064341dup, NC_000012.11:g.65064335_65064341dup, XM_017019182.2:c.-3804_-3799del, XM_017019182.2:c.-3803_-3799del, XM_017019182.2:c.-3802_-3799del, XM_017019182.2:c.-3801_-3799del, XM_017019182.2:c.-3800_-3799del, XM_017019182.2:c.-3799del, XM_017019182.2:c.-3799dup, XM_017019182.2:c.-3800_-3799dup, XM_017019182.2:c.-3801_-3799dup, XM_017019182.2:c.-3802_-3799dup, XM_017019182.2:c.-3803_-3799dup, XM_017019182.2:c.-3805_-3799dup

                                    18.

                                    rs1491342976 has merged into rs10688391 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      GTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
                                      Chromosome:
                                      12:64689235 (GRCh38)
                                      12:65083015 (GRCh37)
                                      Canonical SPDI:
                                      NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000012.12:64689220:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                                      Gene:
                                      RASSF3 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      GTGTGTGTGTGTGTGT=0./0 (ALFA)
                                      -=0.325/13 (GENOME_DK)
                                      GTGTGTGTGT=0.3265/1635 (1000Genomes)
                                      HGVS:
                                      NC_000012.12:g.64689221GT[7], NC_000012.12:g.64689221GT[8], NC_000012.12:g.64689221GT[9], NC_000012.12:g.64689221GT[10], NC_000012.12:g.64689221GT[11], NC_000012.12:g.64689221GT[12], NC_000012.12:g.64689221GT[14], NC_000012.12:g.64689221GT[15], NC_000012.12:g.64689221GT[16], NC_000012.12:g.64689221GT[17], NC_000012.12:g.64689221GT[18], NC_000012.12:g.64689221GT[19], NC_000012.12:g.64689221GT[20], NC_000012.12:g.64689221GT[21], NC_000012.12:g.64689221GT[22], NC_000012.12:g.64689221GT[23], NC_000012.12:g.64689221GT[24], NC_000012.12:g.64689221GT[26], NC_000012.11:g.65083001GT[7], NC_000012.11:g.65083001GT[8], NC_000012.11:g.65083001GT[9], NC_000012.11:g.65083001GT[10], NC_000012.11:g.65083001GT[11], NC_000012.11:g.65083001GT[12], NC_000012.11:g.65083001GT[14], NC_000012.11:g.65083001GT[15], NC_000012.11:g.65083001GT[16], NC_000012.11:g.65083001GT[17], NC_000012.11:g.65083001GT[18], NC_000012.11:g.65083001GT[19], NC_000012.11:g.65083001GT[20], NC_000012.11:g.65083001GT[21], NC_000012.11:g.65083001GT[22], NC_000012.11:g.65083001GT[23], NC_000012.11:g.65083001GT[24], NC_000012.11:g.65083001GT[26]

                                      19.

                                      rs1491283214 has merged into rs772275438 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
                                        Chromosome:
                                        12:64641650 (GRCh38)
                                        12:65035430 (GRCh37)
                                        Canonical SPDI:
                                        NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000012.12:64641637:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
                                        Gene:
                                        RASSF3 (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TTTTTTTTTTTTT=0./0 (ALFA)
                                        -=0.000004/1 (TOPMED)
                                        -=0.056995/22 (NorthernSweden)
                                        -=0.125/5 (GENOME_DK)
                                        HGVS:

                                        20.

                                        rs1491261261 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          ->T [Show Flanks]
                                          Chromosome:
                                          12:64634761 (GRCh38)
                                          12:65028542 (GRCh37)
                                          Canonical SPDI:
                                          NC_000012.12:64634761:T:TT
                                          Gene:
                                          RASSF3 (Varview)
                                          Functional Consequence:
                                          genic_upstream_transcript_variant,intron_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          T=0.00002/1 (GnomAD)
                                          HGVS:

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