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Links from Gene

Items: 1 to 20 of 966

1.

rs1490665087 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    12:10808455 (GRCh38)
    12:10961054 (GRCh37)
    Canonical SPDI:
    NC_000012.12:10808454:C:G
    Gene:
    TAS2R8 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    G=0./0 (ALFA)
    G=0.000011/3 (TOPMED)
    HGVS:
    2.

    rs1490174350 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>C [Show Flanks]
      Chromosome:
      12:10808038 (GRCh38)
      12:10960637 (GRCh37)
      Canonical SPDI:
      NC_000012.12:10808037:A:C
      Gene:
      TAS2R8 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      C=0./0 (ALFA)
      C=0.000004/1 (TOPMED)
      HGVS:
      3.

      rs1490144098 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C [Show Flanks]
        Chromosome:
        12:10807102 (GRCh38)
        12:10959701 (GRCh37)
        Canonical SPDI:
        NC_000012.12:10807101:T:C
        Gene:
        TAS2R8 (Varview)
        Functional Consequence:
        5_prime_UTR_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0./0 (ALFA)
        C=0.000004/1 (TOPMED)
        HGVS:
        4.

        rs1489236468 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          12:10808419 (GRCh38)
          12:10961018 (GRCh37)
          Canonical SPDI:
          NC_000012.12:10808418:G:A
          Gene:
          TAS2R8 (Varview)
          Functional Consequence:
          2KB_upstream_variant,upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          A=0.000011/3 (TOPMED)
          A=0.000021/3 (GnomAD)
          HGVS:
          5.

          rs1487604588 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A,C [Show Flanks]
            Chromosome:
            12:10807374 (GRCh38)
            12:10959973 (GRCh37)
            Canonical SPDI:
            NC_000012.12:10807373:G:A,NC_000012.12:10807373:G:C
            Gene:
            TAS2R8 (Varview)
            Functional Consequence:
            2KB_upstream_variant,upstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0./0 (ALFA)
            C=0.000004/1 (TOPMED)
            A=0.001574/7 (Estonian)
            HGVS:
            6.

            rs1487287489 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              12:10808871 (GRCh38)
              12:10961470 (GRCh37)
              Canonical SPDI:
              NC_000012.12:10808870:T:C
              Gene:
              TAS2R9 (Varview), TAS2R8 (Varview)
              Functional Consequence:
              downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              C=0.000007/1 (GnomAD)
              C=0.000023/6 (TOPMED)
              HGVS:
              7.

              rs1487225844 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                12:10808025 (GRCh38)
                12:10960624 (GRCh37)
                Canonical SPDI:
                NC_000012.12:10808024:G:A
                Gene:
                TAS2R8 (Varview)
                Functional Consequence:
                2KB_upstream_variant,upstream_transcript_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                A=0.000004/1 (TOPMED)
                A=0.000007/1 (GnomAD)
                HGVS:
                8.

                rs1486749362 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A [Show Flanks]
                  Chromosome:
                  12:10808866 (GRCh38)
                  12:10961465 (GRCh37)
                  Canonical SPDI:
                  NC_000012.12:10808865:G:A
                  Gene:
                  TAS2R9 (Varview), TAS2R8 (Varview)
                  Functional Consequence:
                  downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,upstream_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  A=0./0 (ALFA)
                  A=0.000004/1 (TOPMED)
                  HGVS:
                  9.

                  rs1486116543 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    12:10806214 (GRCh38)
                    12:10958813 (GRCh37)
                    Canonical SPDI:
                    NC_000012.12:10806213:A:G
                    Gene:
                    TAS2R8 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,missense_variant
                    Validated:
                    by frequency
                    MAF:
                    G=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    10.

                    rs1485132301 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>A [Show Flanks]
                      Chromosome:
                      12:10806050 (GRCh38)
                      12:10958649 (GRCh37)
                      Canonical SPDI:
                      NC_000012.12:10806049:T:A
                      Gene:
                      TAS2R8 (Varview)
                      Functional Consequence:
                      downstream_transcript_variant,500B_downstream_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      A=0.000007/1 (GnomAD)
                      HGVS:
                      11.

                      rs1483477554 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        12:10808446 (GRCh38)
                        12:10961045 (GRCh37)
                        Canonical SPDI:
                        NC_000012.12:10808445:T:C
                        Gene:
                        TAS2R8 (Varview)
                        Functional Consequence:
                        2KB_upstream_variant,upstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000007/1 (GnomAD)
                        HGVS:
                        12.

                        rs1482311754 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          12:10805736 (GRCh38)
                          12:10958335 (GRCh37)
                          Canonical SPDI:
                          NC_000012.12:10805735:T:C
                          Gene:
                          TAS2R8 (Varview)
                          Functional Consequence:
                          downstream_transcript_variant,500B_downstream_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000008/2 (TOPMED)
                          C=0.000014/2 (GnomAD)
                          HGVS:
                          13.

                          rs1480935360 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            12:10808533 (GRCh38)
                            12:10961132 (GRCh37)
                            Canonical SPDI:
                            NC_000012.12:10808532:T:C
                            Gene:
                            TAS2R8 (Varview)
                            Functional Consequence:
                            upstream_transcript_variant,2KB_upstream_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000004/1 (TOPMED)
                            C=0.000007/1 (GnomAD)
                            HGVS:
                            14.

                            rs1480911210 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>A [Show Flanks]
                              Chromosome:
                              12:10806902 (GRCh38)
                              12:10959501 (GRCh37)
                              Canonical SPDI:
                              NC_000012.12:10806901:T:A
                              Gene:
                              TAS2R8 (Varview)
                              Functional Consequence:
                              coding_sequence_variant,missense_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              A=0.000031/1 (ALFA)
                              A=0.000004/1 (TOPMED)
                              A=0.000014/2 (GnomAD)
                              HGVS:
                              15.

                              rs1479953138 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                12:10808097 (GRCh38)
                                12:10960696 (GRCh37)
                                Canonical SPDI:
                                NC_000012.12:10808096:C:T
                                Gene:
                                TAS2R8 (Varview)
                                Functional Consequence:
                                upstream_transcript_variant,2KB_upstream_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                HGVS:
                                16.

                                rs1478771030 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  12:10805780 (GRCh38)
                                  12:10958379 (GRCh37)
                                  Canonical SPDI:
                                  NC_000012.12:10805779:T:C
                                  Gene:
                                  TAS2R8 (Varview)
                                  Functional Consequence:
                                  downstream_transcript_variant,500B_downstream_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0.000142/2 (ALFA)
                                  C=0.00003/8 (TOPMED)
                                  C=0.000043/6 (GnomAD)
                                  HGVS:
                                  17.

                                  rs1478740811 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    12:10808233 (GRCh38)
                                    12:10960832 (GRCh37)
                                    Canonical SPDI:
                                    NC_000012.12:10808232:A:G
                                    Gene:
                                    TAS2R8 (Varview)
                                    Functional Consequence:
                                    upstream_transcript_variant,2KB_upstream_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000004/1 (TOPMED)
                                    G=0.000007/1 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1478078728 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      12:10805630 (GRCh38)
                                      12:10958229 (GRCh37)
                                      Canonical SPDI:
                                      NC_000012.12:10805629:T:C
                                      Gene:
                                      TAS2R8 (Varview)
                                      Functional Consequence:
                                      downstream_transcript_variant,500B_downstream_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000004/1 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1478049214 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        12:10806620 (GRCh38)
                                        12:10959219 (GRCh37)
                                        Canonical SPDI:
                                        NC_000012.12:10806619:A:G
                                        Gene:
                                        TAS2R8 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        G=0.000007/1 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1477175801 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>C,G [Show Flanks]
                                          Chromosome:
                                          12:10805560 (GRCh38)
                                          12:10958159 (GRCh37)
                                          Canonical SPDI:
                                          NC_000012.12:10805559:A:C,NC_000012.12:10805559:A:G
                                          Gene:
                                          TAS2R8 (Varview)
                                          Functional Consequence:
                                          downstream_transcript_variant,500B_downstream_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000007/1 (GnomAD)
                                          HGVS:

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