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Links from Gene

Items: 1 to 20 of 929

1.

rs1491086667 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    CA>- [Show Flanks]
    Chromosome:
    14:21572608 (GRCh38)
    14:22040751 (GRCh37)
    Canonical SPDI:
    NC_000014.9:21572606:ACA:A
    Gene:
    OR10G3 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    A=0.00017/2 (ALFA)
    HGVS:
    2.

    rs1489803500 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      14:21571801 (GRCh38)
      14:22039933 (GRCh37)
      Canonical SPDI:
      NC_000014.9:21571800:G:A
      Gene:
      OR10G3 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0./0 (ALFA)
      HGVS:
      3.

      rs1489447531 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        14:21571223 (GRCh38)
        14:22039354 (GRCh37)
        Canonical SPDI:
        NC_000014.9:21571222:C:T
        Gene:
        OR10G3 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000004/1 (TOPMED)
        HGVS:
        4.

        rs1489292447 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          14:21571925 (GRCh38)
          14:22040057 (GRCh37)
          Canonical SPDI:
          NC_000014.9:21571924:T:C
          Gene:
          OR10G3 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          C=0./0 (ALFA)
          C=0.000004/1 (TOPMED)
          HGVS:
          5.

          rs1487890705 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>T [Show Flanks]
            Chromosome:
            14:21572263 (GRCh38)
            14:22040395 (GRCh37)
            Canonical SPDI:
            NC_000014.9:21572262:G:T
            Gene:
            OR10G3 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            T=0.00001/1 (GnomAD)
            HGVS:
            6.

            rs1487845610 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>C [Show Flanks]
              Chromosome:
              14:21572547 (GRCh38)
              14:22040688 (GRCh37)
              Canonical SPDI:
              NC_000014.9:21572546:A:C
              Gene:
              OR10G3 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              C=0./0 (ALFA)
              C=0.000007/1 (GnomAD)
              HGVS:
              7.

              rs1487617084 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                14:21570841 (GRCh38)
                14:22038972 (GRCh37)
                Canonical SPDI:
                NC_000014.9:21570840:G:A
                Gene:
                OR10G3 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                A=0.000011/3 (TOPMED)
                A=0.000014/2 (GnomAD)
                HGVS:
                8.

                rs1487455219 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  14:21569687 (GRCh38)
                  14:22037818 (GRCh37)
                  Canonical SPDI:
                  NC_000014.9:21569686:A:G
                  Gene:
                  OR10G3 (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  HGVS:
                  9.

                  rs1487411741 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>C,G [Show Flanks]
                    Chromosome:
                    14:21572217 (GRCh38)
                    14:22040349 (GRCh37)
                    Canonical SPDI:
                    NC_000014.9:21572216:A:C,NC_000014.9:21572216:A:G
                    Gene:
                    OR10G3 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    HGVS:
                    10.

                    rs1487341587 has merged into rs397852312 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AAAAAAAAAAAAAA>-,A,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                      Chromosome:
                      14:21572618 (GRCh38)
                      14:22040759 (GRCh37)
                      Canonical SPDI:
                      NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                      Gene:
                      OR10G3 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAAAAAAA=0./0 (ALFA)
                      HGVS:
                      NC_000014.9:g.21572618_21572631del, NC_000014.9:g.21572619_21572631del, NC_000014.9:g.21572624_21572631del, NC_000014.9:g.21572625_21572631del, NC_000014.9:g.21572626_21572631del, NC_000014.9:g.21572627_21572631del, NC_000014.9:g.21572628_21572631del, NC_000014.9:g.21572629_21572631del, NC_000014.9:g.21572630_21572631del, NC_000014.9:g.21572631del, NC_000014.9:g.21572631dup, NC_000014.9:g.21572630_21572631dup, NC_000014.9:g.21572629_21572631dup, NC_000014.9:g.21572628_21572631dup, NC_000014.9:g.21572627_21572631dup, NC_000014.9:g.21572626_21572631dup, NC_000014.9:g.21572625_21572631dup, NC_000014.9:g.21572624_21572631dup, NC_000014.9:g.21572623_21572631dup, NC_000014.9:g.21572622_21572631dup, NC_000014.9:g.21572621_21572631dup, NC_000014.9:g.21572620_21572631dup, NC_000014.9:g.21572619_21572631dup, NC_000014.9:g.21572618_21572631dup, NC_000014.9:g.21572617_21572631dup, NC_000014.9:g.21572616_21572631dup, NC_000014.9:g.21572615_21572631dup, NC_000014.9:g.21572614_21572631dup, NC_000014.9:g.21572611_21572631dup, NC_000014.9:g.21572610_21572631dup, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040767_22040769dup, NC_000014.8:g.22040759_22040769del, NC_000014.8:g.22040760_22040769del, NC_000014.8:g.22040765_22040769del, NC_000014.8:g.22040766_22040769del, NC_000014.8:g.22040767_22040769del, NC_000014.8:g.22040768_22040769del, NC_000014.8:g.22040769del, NC_000014.8:g.22040769dup, NC_000014.8:g.22040768_22040769dup, NC_000014.8:g.22040766_22040769dup, NC_000014.8:g.22040765_22040769dup, NC_000014.8:g.22040764_22040769dup, NC_000014.8:g.22040763_22040769dup, NC_000014.8:g.22040762_22040769dup, NC_000014.8:g.22040761_22040769dup, NC_000014.8:g.22040760_22040769dup, NC_000014.8:g.22040759_22040769dup, NC_000014.8:g.22040758_22040769dup, NC_000014.8:g.22040757_22040769dup, NC_000014.8:g.22040756_22040769dup, NC_000014.8:g.22040755_22040769dup, NC_000014.8:g.22040754_22040769dup, NC_000014.8:g.22040753_22040769dup, NC_000014.8:g.22040752_22040769dup, NC_000014.8:g.22040751_22040769dup, NC_000014.8:g.22040750_22040769dup, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                      11.

                      rs1486198876 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>T [Show Flanks]
                        Chromosome:
                        14:21569498 (GRCh38)
                        14:22037629 (GRCh37)
                        Canonical SPDI:
                        NC_000014.9:21569497:G:T
                        Gene:
                        OR10G3 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (TOPMED)
                        HGVS:
                        12.

                        rs1485081185 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          14:21572166 (GRCh38)
                          14:22040298 (GRCh37)
                          Canonical SPDI:
                          NC_000014.9:21572165:C:T
                          Gene:
                          OR10G3 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000004/1 (TOPMED)
                          HGVS:
                          13.

                          rs1484286302 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>T [Show Flanks]
                            Chromosome:
                            14:21571694 (GRCh38)
                            14:22039826 (GRCh37)
                            Canonical SPDI:
                            NC_000014.9:21571693:G:T
                            Gene:
                            OR10G3 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            T=0./0 (ALFA)
                            HGVS:
                            14.

                            rs1483808559 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              14:21570135 (GRCh38)
                              14:22038266 (GRCh37)
                              Canonical SPDI:
                              NC_000014.9:21570134:T:C
                              Gene:
                              OR10G3 (Varview)
                              Functional Consequence:
                              coding_sequence_variant,missense_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (GnomAD_exomes)
                              C=0.000007/1 (GnomAD)
                              HGVS:
                              15.

                              rs1483228918 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                14:21569939 (GRCh38)
                                14:22038070 (GRCh37)
                                Canonical SPDI:
                                NC_000014.9:21569938:A:G
                                Gene:
                                OR10G3 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,missense_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000004/1 (GnomAD_exomes)
                                G=0.000004/1 (TOPMED)
                                HGVS:
                                16.

                                rs1483108334 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  14:21572744 (GRCh38)
                                  14:22040882 (GRCh37)
                                  Canonical SPDI:
                                  NC_000014.9:21572743:G:A
                                  Gene:
                                  OR10G3 (Varview)
                                  Functional Consequence:
                                  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:
                                  17.

                                  rs1482441171 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>C [Show Flanks]
                                    Chromosome:
                                    14:21569319 (GRCh38)
                                    14:22037450 (GRCh37)
                                    Canonical SPDI:
                                    NC_000014.9:21569318:G:C
                                    Gene:
                                    OR10G3 (Varview)
                                    Functional Consequence:
                                    3_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0./0 (ALFA)
                                    C=0.000004/1 (TOPMED)
                                    C=0.000007/1 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1481375849 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>A [Show Flanks]
                                      Chromosome:
                                      14:21569933 (GRCh38)
                                      14:22038064 (GRCh37)
                                      Canonical SPDI:
                                      NC_000014.9:21569932:C:A
                                      Gene:
                                      OR10G3 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0.000071/1 (ALFA)
                                      A=0.000007/1 (GnomAD)
                                      A=0.000019/5 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1480778978 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>G,T [Show Flanks]
                                        Chromosome:
                                        14:21570943 (GRCh38)
                                        14:22039074 (GRCh37)
                                        Canonical SPDI:
                                        NC_000014.9:21570942:C:G,NC_000014.9:21570942:C:T
                                        Gene:
                                        OR10G3 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        HGVS:
                                        20.

                                        rs1480281694 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          14:21570010 (GRCh38)
                                          14:22038141 (GRCh37)
                                          Canonical SPDI:
                                          NC_000014.9:21570009:A:G
                                          Gene:
                                          OR10G3 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          G=0.000004/1 (GnomAD_exomes)
                                          HGVS:

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