U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 1000

1.

rs1491571915 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AT>- [Show Flanks]
    Chromosome:
    14:70744467 (GRCh38)
    14:71211184 (GRCh37)
    Canonical SPDI:
    NC_000014.9:70744464:ATAT:AT
    Gene:
    MAP3K9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ATAT=0./0 (ALFA)
    -=0.000019/5 (TOPMED)
    -=0.000029/4 (GnomAD)
    HGVS:

    2.

    rs1491505637 has merged into rs34648545 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ACACACAC>-,ACAC,ACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC [Show Flanks]
      Chromosome:
      14:70725844 (GRCh38)
      14:71192561 (GRCh37)
      Canonical SPDI:
      NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000014.9:70725830:CACACACACACACACACACAC:CACACACACACACACACACACACACACAC
      Gene:
      MAP3K9 (Varview)
      Functional Consequence:
      3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      CACACACACACACACAC=0./0 (ALFA)
      -=0.3919/1772 (1000Genomes)
      HGVS:
      NC_000014.9:g.70725832AC[6], NC_000014.9:g.70725832AC[8], NC_000014.9:g.70725832AC[9], NC_000014.9:g.70725832AC[11], NC_000014.9:g.70725832AC[12], NC_000014.9:g.70725832AC[13], NC_000014.9:g.70725832AC[14], NC_000014.8:g.71192549AC[6], NC_000014.8:g.71192549AC[8], NC_000014.8:g.71192549AC[9], NC_000014.8:g.71192549AC[11], NC_000014.8:g.71192549AC[12], NC_000014.8:g.71192549AC[13], NC_000014.8:g.71192549AC[14], XM_005267683.6:c.*4530TG[6], XM_005267683.6:c.*4530TG[8], XM_005267683.6:c.*4530TG[9], XM_005267683.6:c.*4530TG[11], XM_005267683.6:c.*4530TG[12], XM_005267683.6:c.*4530TG[13], XM_005267683.6:c.*4530TG[14], XM_005267683.5:c.*4530TG[6], XM_005267683.5:c.*4530TG[8], XM_005267683.5:c.*4530TG[9], XM_005267683.5:c.*4530TG[11], XM_005267683.5:c.*4530TG[12], XM_005267683.5:c.*4530TG[13], XM_005267683.5:c.*4530TG[14], XM_005267683.4:c.*4530TG[6], XM_005267683.4:c.*4530TG[8], XM_005267683.4:c.*4530TG[9], XM_005267683.4:c.*4530TG[11], XM_005267683.4:c.*4530TG[12], XM_005267683.4:c.*4530TG[13], XM_005267683.4:c.*4530TG[14], XM_005267683.3:c.*4530TG[6], XM_005267683.3:c.*4530TG[8], XM_005267683.3:c.*4530TG[9], XM_005267683.3:c.*4530TG[11], XM_005267683.3:c.*4530TG[12], XM_005267683.3:c.*4530TG[13], XM_005267683.3:c.*4530TG[14], XM_005267683.2:c.*4530TG[6], XM_005267683.2:c.*4530TG[8], XM_005267683.2:c.*4530TG[9], XM_005267683.2:c.*4530TG[11], XM_005267683.2:c.*4530TG[12], XM_005267683.2:c.*4530TG[13], XM_005267683.2:c.*4530TG[14], XM_005267683.1:c.*4530TG[6], XM_005267683.1:c.*4530TG[8], XM_005267683.1:c.*4530TG[9], XM_005267683.1:c.*4530TG[11], XM_005267683.1:c.*4530TG[12], XM_005267683.1:c.*4530TG[13], XM_005267683.1:c.*4530TG[14], XM_011536788.4:c.*4530TG[6], XM_011536788.4:c.*4530TG[8], XM_011536788.4:c.*4530TG[9], XM_011536788.4:c.*4530TG[11], XM_011536788.4:c.*4530TG[12], XM_011536788.4:c.*4530TG[13], XM_011536788.4:c.*4530TG[14], XM_011536788.3:c.*4530TG[6], XM_011536788.3:c.*4530TG[8], XM_011536788.3:c.*4530TG[9], XM_011536788.3:c.*4530TG[11], XM_011536788.3:c.*4530TG[12], XM_011536788.3:c.*4530TG[13], XM_011536788.3:c.*4530TG[14], XM_011536788.2:c.*4530TG[6], XM_011536788.2:c.*4530TG[8], XM_011536788.2:c.*4530TG[9], XM_011536788.2:c.*4530TG[11], XM_011536788.2:c.*4530TG[12], XM_011536788.2:c.*4530TG[13], XM_011536788.2:c.*4530TG[14], XM_011536788.1:c.*4530TG[6], XM_011536788.1:c.*4530TG[8], XM_011536788.1:c.*4530TG[9], XM_011536788.1:c.*4530TG[11], XM_011536788.1:c.*4530TG[12], XM_011536788.1:c.*4530TG[13], XM_011536788.1:c.*4530TG[14], NM_033141.4:c.*4530TG[6], NM_033141.4:c.*4530TG[8], NM_033141.4:c.*4530TG[9], NM_033141.4:c.*4530TG[11], NM_033141.4:c.*4530TG[12], NM_033141.4:c.*4530TG[13], NM_033141.4:c.*4530TG[14], NM_033141.3:c.*4530TG[6], NM_033141.3:c.*4530TG[8], NM_033141.3:c.*4530TG[9], NM_033141.3:c.*4530TG[11], NM_033141.3:c.*4530TG[12], NM_033141.3:c.*4530TG[13], NM_033141.3:c.*4530TG[14], XM_011536794.3:c.*4530TG[6], XM_011536794.3:c.*4530TG[8], XM_011536794.3:c.*4530TG[9], XM_011536794.3:c.*4530TG[11], XM_011536794.3:c.*4530TG[12], XM_011536794.3:c.*4530TG[13], XM_011536794.3:c.*4530TG[14], XM_011536794.2:c.*4530TG[6], XM_011536794.2:c.*4530TG[8], XM_011536794.2:c.*4530TG[9], XM_011536794.2:c.*4530TG[11], XM_011536794.2:c.*4530TG[12], XM_011536794.2:c.*4530TG[13], XM_011536794.2:c.*4530TG[14], XM_011536794.1:c.*4530TG[6], XM_011536794.1:c.*4530TG[8], XM_011536794.1:c.*4530TG[9], XM_011536794.1:c.*4530TG[11], XM_011536794.1:c.*4530TG[12], XM_011536794.1:c.*4530TG[13], XM_011536794.1:c.*4530TG[14], NM_001284230.2:c.*4530TG[6], NM_001284230.2:c.*4530TG[8], NM_001284230.2:c.*4530TG[9], NM_001284230.2:c.*4530TG[11], NM_001284230.2:c.*4530TG[12], NM_001284230.2:c.*4530TG[13], NM_001284230.2:c.*4530TG[14], NM_001284230.1:c.*4530TG[6], NM_001284230.1:c.*4530TG[8], NM_001284230.1:c.*4530TG[9], NM_001284230.1:c.*4530TG[11], NM_001284230.1:c.*4530TG[12], NM_001284230.1:c.*4530TG[13], NM_001284230.1:c.*4530TG[14], XM_011536792.1:c.*4530TG[6], XM_011536792.1:c.*4530TG[8], XM_011536792.1:c.*4530TG[9], XM_011536792.1:c.*4530TG[11], XM_011536792.1:c.*4530TG[12], XM_011536792.1:c.*4530TG[13], XM_011536792.1:c.*4530TG[14], NM_001284231.1:c.*4530TG[6], NM_001284231.1:c.*4530TG[8], NM_001284231.1:c.*4530TG[9], NM_001284231.1:c.*4530TG[11], NM_001284231.1:c.*4530TG[12], NM_001284231.1:c.*4530TG[13], NM_001284231.1:c.*4530TG[14], NM_001284232.1:c.*4530TG[6], NM_001284232.1:c.*4530TG[8], NM_001284232.1:c.*4530TG[9], NM_001284232.1:c.*4530TG[11], NM_001284232.1:c.*4530TG[12], NM_001284232.1:c.*4530TG[13], NM_001284232.1:c.*4530TG[14]

      3.

      rs1491500799 has merged into rs1170327816 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        14:70798484 (GRCh38)
        14:71265201 (GRCh37)
        Canonical SPDI:
        NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:70798471:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        MAP3K9 (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTTTTTTTTTTT=0./0 (ALFA)
        -=0.000015/4 (TOPMED)
        HGVS:
        NC_000014.9:g.70798484_70798496del, NC_000014.9:g.70798485_70798496del, NC_000014.9:g.70798486_70798496del, NC_000014.9:g.70798487_70798496del, NC_000014.9:g.70798488_70798496del, NC_000014.9:g.70798489_70798496del, NC_000014.9:g.70798490_70798496del, NC_000014.9:g.70798491_70798496del, NC_000014.9:g.70798492_70798496del, NC_000014.9:g.70798493_70798496del, NC_000014.9:g.70798494_70798496del, NC_000014.9:g.70798495_70798496del, NC_000014.9:g.70798496del, NC_000014.9:g.70798496dup, NC_000014.9:g.70798495_70798496dup, NC_000014.9:g.70798494_70798496dup, NC_000014.9:g.70798493_70798496dup, NC_000014.9:g.70798492_70798496dup, NC_000014.9:g.70798491_70798496dup, NC_000014.9:g.70798490_70798496dup, NC_000014.9:g.70798489_70798496dup, NC_000014.9:g.70798488_70798496dup, NC_000014.9:g.70798487_70798496dup, NC_000014.9:g.70798485_70798496dup, NC_000014.9:g.70798484_70798496dup, NC_000014.9:g.70798483_70798496dup, NC_000014.9:g.70798482_70798496dup, NC_000014.9:g.70798480_70798496dup, NC_000014.9:g.70798496_70798497insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.71265201_71265213del, NC_000014.8:g.71265202_71265213del, NC_000014.8:g.71265203_71265213del, NC_000014.8:g.71265204_71265213del, NC_000014.8:g.71265205_71265213del, NC_000014.8:g.71265206_71265213del, NC_000014.8:g.71265207_71265213del, NC_000014.8:g.71265208_71265213del, NC_000014.8:g.71265209_71265213del, NC_000014.8:g.71265210_71265213del, NC_000014.8:g.71265211_71265213del, NC_000014.8:g.71265212_71265213del, NC_000014.8:g.71265213del, NC_000014.8:g.71265213dup, NC_000014.8:g.71265212_71265213dup, NC_000014.8:g.71265211_71265213dup, NC_000014.8:g.71265210_71265213dup, NC_000014.8:g.71265209_71265213dup, NC_000014.8:g.71265208_71265213dup, NC_000014.8:g.71265207_71265213dup, NC_000014.8:g.71265206_71265213dup, NC_000014.8:g.71265205_71265213dup, NC_000014.8:g.71265204_71265213dup, NC_000014.8:g.71265202_71265213dup, NC_000014.8:g.71265201_71265213dup, NC_000014.8:g.71265200_71265213dup, NC_000014.8:g.71265199_71265213dup, NC_000014.8:g.71265197_71265213dup, NC_000014.8:g.71265213_71265214insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

        4.

        rs1491445851 has merged into rs10523480 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AAA>-,A,AA,AAAA,AAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAA [Show Flanks]
          Chromosome:
          14:70765748 (GRCh38)
          14:71232465 (GRCh37)
          Canonical SPDI:
          NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAA
          Gene:
          MAP3K9 (Varview)
          Functional Consequence:
          intron_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          AAAAAAAAAAAAA=0./0 (ALFA)
          HGVS:

          5.

          rs1491366664 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            TA>- [Show Flanks]
            Chromosome:
            14:70765735 (GRCh38)
            14:71232452 (GRCh37)
            Canonical SPDI:
            NC_000014.9:70765734:TA:
            Gene:
            MAP3K9 (Varview)
            Functional Consequence:
            genic_upstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            -=0.00017/2 (ALFA)
            -=0.00025/4 (TOMMO)
            HGVS:

            6.

            rs1491304406 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              ->CTTTCTTTTCTTTTCTTTTC
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491299718 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                GC>- [Show Flanks]
                Chromosome:
                14:70760141 (GRCh38)
                14:71226858 (GRCh37)
                Canonical SPDI:
                NC_000014.9:70760140:GC:
                Gene:
                MAP3K9 (Varview)
                Functional Consequence:
                upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                -=0./0 (ALFA)
                -=0.00013/5 (GnomAD)
                HGVS:

                8.

                rs1491262010 [Homo sapiens]
                  Variant type:
                  INS
                  Alleles:
                  ->AAAAAAAAAAAAAAAAAAAAAAAAT,AAAAAAAAAAAAAAAC [Show Flanks]
                  Chromosome:
                  14:70775015 (GRCh38)
                  14:71241733 (GRCh37)
                  Canonical SPDI:
                  NC_000014.9:70775015::AAAAAAAAAAAAAAAAAAAAAAAAT,NC_000014.9:70775015::AAAAAAAAAAAAAAAC
                  Gene:
                  MAP3K9 (Varview)
                  Functional Consequence:
                  genic_upstream_transcript_variant,intron_variant
                  HGVS:

                  9.

                  rs1491257164 [Homo sapiens]
                    Variant type:
                    SNV:
                    Alleles:
                    ->AACACA
                    Chromosome:
                    no mapping
                    Canonical SPDI:

                    10.

                    rs1491221929 [Homo sapiens]
                      Variant type:
                      INS
                      Alleles:
                      ->A [Show Flanks]
                      Chromosome:
                      14:70742910 (GRCh38)
                      14:71209628 (GRCh37)
                      Canonical SPDI:
                      NC_000014.9:70742910::A
                      Gene:
                      MAP3K9 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      A=0.00007/2 (TOMMO)
                      A=0.00614/193 (GnomAD)
                      HGVS:

                      11.

                      rs1491184715 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->GTTT [Show Flanks]
                        Chromosome:
                        14:70798472 (GRCh38)
                        14:71265190 (GRCh37)
                        Canonical SPDI:
                        NC_000014.9:70798472:TTT:TTTGTTT
                        Gene:
                        MAP3K9 (Varview)
                        Functional Consequence:
                        genic_upstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        TTTGTTT=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1491179120 has merged into rs60112409 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          CACACACACACACACACACA>-,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACA [Show Flanks]
                          Chromosome:
                          14:70760154 (GRCh38)
                          14:71226871 (GRCh37)
                          Canonical SPDI:
                          NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACA,NC_000014.9:70760141:CACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACA
                          Gene:
                          MAP3K9 (Varview)
                          Functional Consequence:
                          intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          CACACACACACA=0./0 (ALFA)
                          CACACACA=0.3025/1515 (1000Genomes)
                          HGVS:
                          NC_000014.9:g.70760142CA[6], NC_000014.9:g.70760142CA[8], NC_000014.9:g.70760142CA[9], NC_000014.9:g.70760142CA[10], NC_000014.9:g.70760142CA[11], NC_000014.9:g.70760142CA[12], NC_000014.9:g.70760142CA[13], NC_000014.9:g.70760142CA[14], NC_000014.9:g.70760142CA[15], NC_000014.9:g.70760142CA[17], NC_000014.9:g.70760142CA[18], NC_000014.9:g.70760142CA[19], NC_000014.9:g.70760142CA[20], NC_000014.9:g.70760142CA[21], NC_000014.9:g.70760142CA[22], NC_000014.9:g.70760142CA[23], NC_000014.9:g.70760142CA[24], NC_000014.9:g.70760142CA[25], NC_000014.8:g.71226859CA[6], NC_000014.8:g.71226859CA[8], NC_000014.8:g.71226859CA[9], NC_000014.8:g.71226859CA[10], NC_000014.8:g.71226859CA[11], NC_000014.8:g.71226859CA[12], NC_000014.8:g.71226859CA[13], NC_000014.8:g.71226859CA[14], NC_000014.8:g.71226859CA[15], NC_000014.8:g.71226859CA[17], NC_000014.8:g.71226859CA[18], NC_000014.8:g.71226859CA[19], NC_000014.8:g.71226859CA[20], NC_000014.8:g.71226859CA[21], NC_000014.8:g.71226859CA[22], NC_000014.8:g.71226859CA[23], NC_000014.8:g.71226859CA[24], NC_000014.8:g.71226859CA[25]

                          13.

                          rs1491136287 [Homo sapiens]
                            Variant type:
                            DEL
                            Alleles:
                            TT>- [Show Flanks]
                            Chromosome:
                            14:70739528 (GRCh38)
                            14:71206245 (GRCh37)
                            Canonical SPDI:
                            NC_000014.9:70739527:TT:
                            Gene:
                            MAP3K9 (Varview)
                            Functional Consequence:
                            intron_variant
                            HGVS:

                            14.

                            rs1491090479 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              GA>- [Show Flanks]
                              Chromosome:
                              14:70775016 (GRCh38)
                              14:71241733 (GRCh37)
                              Canonical SPDI:
                              NC_000014.9:70775014:AGA:A
                              Gene:
                              MAP3K9 (Varview)
                              Functional Consequence:
                              genic_upstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              A=0./0 (ALFA)
                              HGVS:

                              15.

                              rs1491025857 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TA>- [Show Flanks]
                                Chromosome:
                                14:70760174 (GRCh38)
                                14:71226891 (GRCh37)
                                Canonical SPDI:
                                NC_000014.9:70760172:ATA:A
                                Gene:
                                MAP3K9 (Varview)
                                Functional Consequence:
                                upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0.003735/61 (ALFA)
                                -=0.000566/9 (TOMMO)
                                -=0.006942/928 (GnomAD)
                                HGVS:

                                16.

                                rs1491015025 has merged into rs141869536 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC [Show Flanks]
                                  Chromosome:
                                  14:70739518 (GRCh38)
                                  14:71206235 (GRCh37)
                                  Canonical SPDI:
                                  NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC
                                  Gene:
                                  MAP3K9 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  CACACACACACACACAC=0./0 (ALFA)
                                  CA=0.425/17 (GENOME_DK)
                                  HGVS:

                                  17.

                                  rs1490930011 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    14:70785095 (GRCh38)
                                    14:71251812 (GRCh37)
                                    Canonical SPDI:
                                    NC_000014.9:70785094:G:A
                                    Gene:
                                    MAP3K9 (Varview)
                                    Functional Consequence:
                                    upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000004/1 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490919131 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      14:70810768 (GRCh38)
                                      14:71277485 (GRCh37)
                                      Canonical SPDI:
                                      NC_000014.9:70810767:C:G
                                      Gene:
                                      MAP3K9 (Varview), MAP3K9-DT (Varview)
                                      Functional Consequence:
                                      upstream_transcript_variant,intron_variant,2KB_upstream_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490874364 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        A>- [Show Flanks]
                                        Chromosome:
                                        14:70754112 (GRCh38)
                                        14:71220829 (GRCh37)
                                        Canonical SPDI:
                                        NC_000014.9:70754111:AA:A
                                        Gene:
                                        MAP3K9 (Varview)
                                        Functional Consequence:
                                        intron_variant,5_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        AA=0./0 (ALFA)
                                        -=0.000008/2 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1490838852 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          14:70793230 (GRCh38)
                                          14:71259947 (GRCh37)
                                          Canonical SPDI:
                                          NC_000014.9:70793229:G:A
                                          Gene:
                                          MAP3K9 (Varview)
                                          Functional Consequence:
                                          genic_upstream_transcript_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000007/1 (GnomAD)
                                          HGVS:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...