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1.

rs1491421192 has merged into rs1197357619 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTTTTTTTTTTTTTTTTTTT>TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    12:49991480
    Gene:
    RACGAP1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by cluster
    HGVS:
    NC_000012.12:g.49991497_49991507del, NC_000012.12:g.49991498_49991507del, NC_000012.12:g.49991499_49991507del, NC_000012.12:g.49991500_49991507del, NC_000012.12:g.49991501_49991507del, NC_000012.12:g.49991502_49991507del, NC_000012.12:g.49991503_49991507del, NC_000012.12:g.49991504_49991507del, NC_000012.12:g.49991505_49991507del, NC_000012.12:g.49991506_49991507del, NC_000012.12:g.49991507del, NC_000012.12:g.49991507dup, NC_000012.12:g.49991506_49991507dup, NC_000012.12:g.49991505_49991507dup, NC_000012.12:g.49991504_49991507dup, NC_000012.12:g.49991503_49991507dup, NC_000012.12:g.49991501_49991507dup, NC_000012.11:g.50385280_50385290del, NC_000012.11:g.50385281_50385290del, NC_000012.11:g.50385282_50385290del, NC_000012.11:g.50385283_50385290del, NC_000012.11:g.50385284_50385290del, NC_000012.11:g.50385285_50385290del, NC_000012.11:g.50385286_50385290del, NC_000012.11:g.50385287_50385290del, NC_000012.11:g.50385288_50385290del, NC_000012.11:g.50385289_50385290del, NC_000012.11:g.50385290del, NC_000012.11:g.50385290dup, NC_000012.11:g.50385289_50385290dup, NC_000012.11:g.50385288_50385290dup, NC_000012.11:g.50385287_50385290dup, NC_000012.11:g.50385286_50385290dup, NC_000012.11:g.50385284_50385290dup
    2.

    rs1491396635 has merged into rs58620170 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAAAAAAAAAAAAAAAA>AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
      Chromosome:
      12:50030349
      Gene:
      RACGAP1 (Varview)
      Functional Consequence:
      genic_upstream_transcript_variant,intron_variant
      Validated:
      by frequency,by cluster
      MAF:
      -=0.0963/357 (TWINSUK)
      -=0.1100/424 (ALSPAC)
      -=0.2760/1382 (1000Genomes)
      HGVS:
      NC_000012.12:g.50030363_50030366del, NC_000012.12:g.50030364_50030366del, NC_000012.12:g.50030365_50030366del, NC_000012.12:g.50030366del, NC_000012.12:g.50030366dup, NC_000012.12:g.50030364_50030366dup, NC_000012.11:g.50424146_50424149del, NC_000012.11:g.50424147_50424149del, NC_000012.11:g.50424148_50424149del, NC_000012.11:g.50424149del, NC_000012.11:g.50424149dup, NC_000012.11:g.50424147_50424149dup
      3.

      rs1491241450 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CA>- [Show Flanks]
        Chromosome:
        12:50030348
        Gene:
        RACGAP1 (Varview)
        Functional Consequence:
        genic_upstream_transcript_variant,intron_variant
        HGVS:
        NC_000012.12:g.50030348_50030349del, NC_000012.11:g.50424131_50424132del
        4.

        rs1491208086 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          G>GTGTGTGTGAG,GTGTGTGTGTGAG,GTGTGTGTGTGTGAG [Show Flanks]
          Chromosome:
          12:50032567
          Gene:
          RACGAP1 (Varview)
          Functional Consequence:
          upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
          Validated:
          by frequency,by cluster
          MAF:
          GTGTGTGTGTGA=0.0000/1 (TOPMED)
          HGVS:
          NC_000012.12:g.50032567_50032568insTGTGTGTGAG, NC_000012.12:g.50032567_50032568insTGTGTGTGTGAG, NC_000012.12:g.50032567_50032568insTGTGTGTGTGTGAG, NC_000012.11:g.50426350_50426351insTGTGTGTGAG, NC_000012.11:g.50426350_50426351insTGTGTGTGTGAG, NC_000012.11:g.50426350_50426351insTGTGTGTGTGTGAG
          5.

          rs1491138880 has merged into rs59257280 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TATATATATATATATATATATAT>TATATATATATAT,TATATATATATATAT,TATATATATATATATAT,TATATATATATATATATAT,TATATATATATATATATATAT,TATATATATATATATATATATATAT,TATATATATATATATATATATATATAT,TATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATATATATATATATATATAT [Show Flanks]
            Chromosome:
            12:49991458
            Gene:
            RACGAP1 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by cluster
            HGVS:
            NC_000012.12:g.49991459_49991460AT[6], NC_000012.12:g.49991459_49991460AT[7], NC_000012.12:g.49991459_49991460AT[8], NC_000012.12:g.49991459_49991460AT[9], NC_000012.12:g.49991459_49991460AT[10], NC_000012.12:g.49991459_49991460AT[12], NC_000012.12:g.49991459_49991460AT[13], NC_000012.12:g.49991459_49991460AT[14], NC_000012.12:g.49991459_49991460AT[15], NC_000012.12:g.49991459_49991460AT[16], NC_000012.12:g.49991459_49991460AT[17], NC_000012.12:g.49991459_49991460AT[18], NC_000012.12:g.49991459_49991460AT[19], NC_000012.12:g.49991459_49991460AT[20], NC_000012.12:g.49991459_49991460AT[21], NC_000012.12:g.49991459_49991460AT[22], NC_000012.12:g.49991459_49991460AT[23], NC_000012.11:g.50385242_50385243AT[6], NC_000012.11:g.50385242_50385243AT[7], NC_000012.11:g.50385242_50385243AT[8], NC_000012.11:g.50385242_50385243AT[9], NC_000012.11:g.50385242_50385243AT[10], NC_000012.11:g.50385242_50385243AT[12], NC_000012.11:g.50385242_50385243AT[13], NC_000012.11:g.50385242_50385243AT[14], NC_000012.11:g.50385242_50385243AT[15], NC_000012.11:g.50385242_50385243AT[16], NC_000012.11:g.50385242_50385243AT[17], NC_000012.11:g.50385242_50385243AT[18], NC_000012.11:g.50385242_50385243AT[19], NC_000012.11:g.50385242_50385243AT[20], NC_000012.11:g.50385242_50385243AT[21], NC_000012.11:g.50385242_50385243AT[22], NC_000012.11:g.50385242_50385243AT[23]
            6.

            rs1491084844 has merged into rs35573059 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              AAAAAAAAAAAAAAAAA>AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
              Chromosome:
              12:50015043
              Gene:
              RACGAP1 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by cluster
              MAF:
              A=0.5377/2693 (1000Genomes)
              HGVS:
              NC_000012.12:g.50015057_50015059del, NC_000012.12:g.50015058_50015059del, NC_000012.12:g.50015059del, NC_000012.12:g.50015059dup, NC_000012.12:g.50015058_50015059dup, NC_000012.12:g.50015057_50015059dup, NC_000012.12:g.50015055_50015059dup, NC_000012.11:g.50408840_50408842del, NC_000012.11:g.50408841_50408842del, NC_000012.11:g.50408842del, NC_000012.11:g.50408842dup, NC_000012.11:g.50408841_50408842dup, NC_000012.11:g.50408840_50408842dup, NC_000012.11:g.50408838_50408842dup
              7.

              rs1491066428 has merged into rs376586076 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTTTTTTTTTTTTTTTTTTTTTT>TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                12:50033555
                Gene:
                RACGAP1 (Varview)
                Functional Consequence:
                upstream_transcript_variant
                Validated:
                by frequency,by cluster
                MAF:
                T=0.9595/3558 (TWINSUK)
                T=0.9611/3704 (ALSPAC)
                HGVS:
                NC_000012.12:g.50033567_50033581del, NC_000012.12:g.50033569_50033581del, NC_000012.12:g.50033570_50033581del, NC_000012.12:g.50033571_50033581del, NC_000012.12:g.50033572_50033581del, NC_000012.12:g.50033573_50033581del, NC_000012.12:g.50033574_50033581del, NC_000012.12:g.50033575_50033581del, NC_000012.12:g.50033576_50033581del, NC_000012.12:g.50033577_50033581del, NC_000012.12:g.50033578_50033581del, NC_000012.12:g.50033579_50033581del, NC_000012.12:g.50033580_50033581del, NC_000012.12:g.50033581del, NC_000012.12:g.50033581dup, NC_000012.12:g.50033580_50033581dup, NC_000012.12:g.50033579_50033581dup, NC_000012.11:g.50427350_50427364del, NC_000012.11:g.50427352_50427364del, NC_000012.11:g.50427353_50427364del, NC_000012.11:g.50427354_50427364del, NC_000012.11:g.50427355_50427364del, NC_000012.11:g.50427356_50427364del, NC_000012.11:g.50427357_50427364del, NC_000012.11:g.50427358_50427364del, NC_000012.11:g.50427359_50427364del, NC_000012.11:g.50427360_50427364del, NC_000012.11:g.50427361_50427364del, NC_000012.11:g.50427362_50427364del, NC_000012.11:g.50427363_50427364del, NC_000012.11:g.50427364del, NC_000012.11:g.50427364dup, NC_000012.11:g.50427363_50427364dup, NC_000012.11:g.50427362_50427364dup
                8.

                rs1491037495 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AGA>A [Show Flanks]
                  Chromosome:
                  12:50002071
                  Gene:
                  RACGAP1 (Varview)
                  Functional Consequence:
                  intron_variant
                  HGVS:
                  NC_000012.12:g.50002072_50002073del, NC_000012.11:g.50395855_50395856del
                  9.

                  rs1490993416 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>G [Show Flanks]
                    Chromosome:
                    12:50033828
                    Gene:
                    RACGAP1 (Varview)
                    Functional Consequence:
                    upstream_transcript_variant
                    Validated:
                    by frequency
                    MAF:
                    G=0.0001/2 (GnomAD)
                    HGVS:
                    NC_000012.12:g.50033828T>G, NC_000012.11:g.50427611T>G
                    10.

                    rs1490949793 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      12:50023306
                      Gene:
                      RACGAP1 (Varview)
                      Functional Consequence:
                      genic_upstream_transcript_variant,intron_variant
                      Validated:
                      by frequency
                      MAF:
                      C=0.0000/1 (TOPMED)
                      HGVS:
                      NC_000012.12:g.50023306T>C, NC_000012.11:g.50417089T>C
                      11.

                      rs1490873884 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        12:49997685
                        Gene:
                        RACGAP1 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by cluster
                        MAF:
                        T=0.0000/1 (GnomAD)
                        T=0.0000/1 (TOPMED)
                        HGVS:
                        NC_000012.12:g.49997685C>T, NC_000012.11:g.50391468C>T
                        12.

                        rs1490853631 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          12:50000010
                          Gene:
                          RACGAP1 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by cluster
                          HGVS:
                          NC_000012.12:g.50000010C>T, NC_000012.11:g.50393793C>T
                          13.

                          rs1490687202 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            TATTTT>T [Show Flanks]
                            Chromosome:
                            12:49991478
                            Gene:
                            RACGAP1 (Varview)
                            Functional Consequence:
                            intron_variant
                            HGVS:
                            NC_000012.12:g.49991479_49991483del, NC_000012.11:g.50385262_50385266del
                            14.

                            rs1490656233 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>T [Show Flanks]
                              Chromosome:
                              12:50031051
                              Gene:
                              RACGAP1 (Varview)
                              Functional Consequence:
                              genic_upstream_transcript_variant,intron_variant
                              Validated:
                              by frequency
                              MAF:
                              T=0.0000/1 (TOPMED)
                              HGVS:
                              NC_000012.12:g.50031051A>T, NC_000012.11:g.50424834A>T
                              15.

                              rs1490591366 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                12:49991234
                                Gene:
                                RACGAP1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.0000/1 (TOPMED)
                                HGVS:
                                NC_000012.12:g.49991234A>G, NC_000012.11:g.50385017A>G
                                16.

                                rs1490542918 has merged into rs71441313 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  AAAAAAAAAAAAAAAAAAAAAAAAA>AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                                  Chromosome:
                                  12:50008170
                                  Gene:
                                  RACGAP1 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by cluster
                                  HGVS:
                                  NC_000012.12:g.50008181_50008194del, NC_000012.12:g.50008183_50008194del, NC_000012.12:g.50008184_50008194del, NC_000012.12:g.50008185_50008194del, NC_000012.12:g.50008186_50008194del, NC_000012.12:g.50008187_50008194del, NC_000012.12:g.50008188_50008194del, NC_000012.12:g.50008189_50008194del, NC_000012.12:g.50008190_50008194del, NC_000012.12:g.50008191_50008194del, NC_000012.12:g.50008192_50008194del, NC_000012.12:g.50008193_50008194del, NC_000012.12:g.50008194del, NC_000012.12:g.50008194dup, NC_000012.12:g.50008193_50008194dup, NC_000012.12:g.50008192_50008194dup, NC_000012.12:g.50008191_50008194dup, NC_000012.12:g.50008190_50008194dup, NC_000012.11:g.50401964_50401977del, NC_000012.11:g.50401966_50401977del, NC_000012.11:g.50401967_50401977del, NC_000012.11:g.50401968_50401977del, NC_000012.11:g.50401969_50401977del, NC_000012.11:g.50401970_50401977del, NC_000012.11:g.50401971_50401977del, NC_000012.11:g.50401972_50401977del, NC_000012.11:g.50401973_50401977del, NC_000012.11:g.50401974_50401977del, NC_000012.11:g.50401975_50401977del, NC_000012.11:g.50401976_50401977del, NC_000012.11:g.50401977del, NC_000012.11:g.50401977dup, NC_000012.11:g.50401976_50401977dup, NC_000012.11:g.50401975_50401977dup, NC_000012.11:g.50401974_50401977dup, NC_000012.11:g.50401973_50401977dup
                                  17.

                                  rs1490502784 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    CCC>CCCCC [Show Flanks]
                                    Chromosome:
                                    12:50032948
                                    Gene:
                                    RACGAP1 (Varview)
                                    Functional Consequence:
                                    upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    CC=0.0000/1 (GnomAD)
                                    HGVS:
                                    NC_000012.12:g.50032949_50032950dup, NC_000012.11:g.50426732_50426733dup
                                    18.

                                    rs1490456126 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      12:49998409
                                      Gene:
                                      RACGAP1 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      G=0.0000/2 (TOPMED)
                                      HGVS:
                                      NC_000012.12:g.49998409A>G, NC_000012.11:g.50392192A>G
                                      19.

                                      rs1490382581 [Homo sapiens]
                                        Variant type:
                                        DEL
                                        Alleles:
                                        AAT>- [Show Flanks]
                                        Chromosome:
                                        12:49996667
                                        Gene:
                                        RACGAP1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency
                                        MAF:
                                        -=0.0000/1 (GnomAD)
                                        HGVS:
                                        NC_000012.12:g.49996667_49996669del, NC_000012.11:g.50390450_50390452del
                                        20.

                                        rs1490356488 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          12:50016307
                                          Gene:
                                          RACGAP1 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          A=0.0000/6 (TOPMED)
                                          HGVS:
                                          NC_000012.12:g.50016307G>A, NC_000012.11:g.50410090G>A

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