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Links from Gene

Items: 1 to 20 of 1314

1.

rs1489972681 [Homo sapiens]
    Variant type:
    SNV:
    Alleles:
    AGG>-
    Chromosome:
    no mapping
    Canonical SPDI:

    2.

    rs1489304713 [Homo sapiens]
      Variant type:
      SNV:
      Alleles:
      A>G
      Chromosome:
      no mapping
      Canonical SPDI:

      3.

      rs1489213262 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        17:38063194 (GRCh38)
        17:-1 (GRCh37)
        Canonical SPDI:
        NC_000017.11:38063193:G:A
        Gene:
        TBC1D3C (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        A=0.00008/1 (ALFA)
        A=0.00016/3 (TOMMO)
        HGVS:

        4.

        rs1488881725 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          NT_187661.1:211844 (GRCh38)
          NT_187661.1:34585109 (GRCh37)
          Canonical SPDI:
          NT_187661.1:211843:G:A
          Gene:
          TBC1D3I (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          A=0.0286/128 (ALFA)
          HGVS:

          5.

          rs1488696901 [Homo sapiens]
            Variant type:
            SNV:
            Alleles:
            C>T
            Chromosome:
            no mapping
            Canonical SPDI:

            6.

            rs1488386191 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>G [Show Flanks]
              Chromosome:
              17:38062898 (GRCh38)
              17:-1 (GRCh37)
              Canonical SPDI:
              NC_000017.11:38062897:T:G
              Gene:
              TBC1D3C (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              G=0.00017/2 (ALFA)
              HGVS:

              7.

              rs1488225986 [Homo sapiens]
                Variant type:
                SNV:
                Alleles:
                T>C
                Chromosome:
                no mapping
                Canonical SPDI:

                8.

                rs1488197223 [Homo sapiens]
                  Variant type:
                  SNV:
                  Alleles:
                  C>G
                  Chromosome:
                  no mapping
                  Canonical SPDI:

                  9.

                  rs1487609071 [Homo sapiens]
                    Variant type:
                    SNV:
                    Alleles:
                    G>A
                    Chromosome:
                    no mapping
                    Canonical SPDI:

                    10.

                    rs1487577375 [Homo sapiens]
                      Variant type:
                      SNV:
                      Alleles:
                      G>A
                      Chromosome:
                      no mapping
                      Canonical SPDI:

                      11.

                      rs1487354093 [Homo sapiens]
                        Variant type:
                        SNV:
                        Alleles:
                        C>T
                        Chromosome:
                        no mapping
                        Canonical SPDI:

                        12.

                        rs1487207943 [Homo sapiens]
                          Variant type:
                          SNV:
                          Alleles:
                          C>T
                          Chromosome:
                          no mapping
                          Canonical SPDI:

                          13.

                          rs1487059202 [Homo sapiens]
                            Variant type:
                            SNV:
                            Alleles:
                            CGG>-
                            Chromosome:
                            no mapping
                            Canonical SPDI:

                            14.

                            rs1486531670 has merged into rs864094 [Homo sapiens]
                              Variant type:
                              SNV:
                              Alleles:
                              A>G,T
                              Chromosome:
                              no mapping
                              Canonical SPDI:

                              15.

                              rs1486394968 [Homo sapiens]
                                Variant type:
                                SNV:
                                Alleles:
                                G>C
                                Chromosome:
                                no mapping
                                Canonical SPDI:

                                16.

                                rs1486347972 [Homo sapiens]
                                  Variant type:
                                  SNV:
                                  Alleles:
                                  C>G
                                  Chromosome:
                                  no mapping
                                  Canonical SPDI:

                                  17.

                                  rs1485743986 [Homo sapiens]
                                    Variant type:
                                    SNV:
                                    Alleles:
                                    C>G
                                    Chromosome:
                                    no mapping
                                    Canonical SPDI:

                                    18.

                                    rs1485621299 [Homo sapiens]
                                      Variant type:
                                      SNV:
                                      Alleles:
                                      G>A
                                      Chromosome:
                                      no mapping
                                      Canonical SPDI:

                                      19.

                                      rs1485589790 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        17:38062879 (GRCh38)
                                        17:-1 (GRCh37)
                                        Canonical SPDI:
                                        NC_000017.11:38062878:C:T
                                        Gene:
                                        TBC1D3C (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0.00008/1 (ALFA)
                                        T=0.00002/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1485559500 [Homo sapiens]
                                          Variant type:
                                          SNV:
                                          Alleles:
                                          C>-
                                          Chromosome:
                                          no mapping
                                          Canonical SPDI:

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