U.S. flag

An official website of the United States government

Links from Gene

Items: 1 to 20 of 2832

1.

rs1490620337 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    3:129318413 (GRCh38)
    3:129037256 (GRCh37)
    Canonical SPDI:
    NC_000003.12:129318412:G:A
    Gene:
    H1-10-AS1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0.000023/6 (TOPMED)
    A=0.000318/5 (TOMMO)
    A=0.000342/1 (KOREAN)
    ...more
    HGVS:
    2.

    rs1490505454 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      3:129320132 (GRCh38)
      3:129038975 (GRCh37)
      Canonical SPDI:
      NC_000003.12:129320131:A:G
      Gene:
      H1-10-AS1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      G=0./0 (ALFA)
      HGVS:
      3.

      rs1490128691 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        3:129317917 (GRCh38)
        3:129036760 (GRCh37)
        Canonical SPDI:
        NC_000003.12:129317916:G:A
        Gene:
        H1-10 (Varview), H1-10-AS1 (Varview)
        Functional Consequence:
        intron_variant,upstream_transcript_variant,2KB_upstream_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.000071/1 (ALFA)
        A=0.000029/4 (GnomAD)
        A=0.00003/8 (TOPMED)
        ...more
        HGVS:
        4.

        rs1490014223 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          3:129319229 (GRCh38)
          3:129038072 (GRCh37)
          Canonical SPDI:
          NC_000003.12:129319228:C:T
          Gene:
          H1-10-AS1 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (TOPMED)
          T=0.000014/2 (GnomAD)
          ...more
          HGVS:
          5.

          rs1489910482 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            3:129324078 (GRCh38)
            3:129042921 (GRCh37)
            Canonical SPDI:
            NC_000003.12:129324077:G:A
            Gene:
            H1-10-AS1 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            A=0./0 (ALFA)
            A=0.000014/2 (GnomAD)
            A=0.000026/7 (TOPMED)
            ...more
            HGVS:
            6.

            rs1489749715 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>T [Show Flanks]
              Chromosome:
              3:129323270 (GRCh38)
              3:129042113 (GRCh37)
              Canonical SPDI:
              NC_000003.12:129323269:G:T
              Gene:
              H1-10-AS1 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0.000071/1 (ALFA)
              T=0.000004/1 (TOPMED)
              T=0.000007/1 (GnomAD)
              ...more
              HGVS:
              7.

              rs1489452472 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>C,T [Show Flanks]
                Chromosome:
                3:129316461 (GRCh38)
                3:129035304 (GRCh37)
                Canonical SPDI:
                NC_000003.12:129316460:G:C,NC_000003.12:129316460:G:T
                Gene:
                H1-10 (Varview), H1-10-AS1 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
                Validated:
                by frequency,by alfa
                MAF:
                T=0./0 (ALFA)
                T=0.000004/1 (TOPMED)
                HGVS:
                8.

                rs1489333478 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A [Show Flanks]
                  Chromosome:
                  3:129315897 (GRCh38)
                  3:129034740 (GRCh37)
                  Canonical SPDI:
                  NC_000003.12:129315896:G:A
                  Gene:
                  H1-10 (Varview), H1-10-AS1 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,upstream_transcript_variant,synonymous_variant,2KB_upstream_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0./0 (ALFA)
                  A=0.000014/2 (GnomAD)
                  HGVS:
                  9.

                  rs1489285447 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>T [Show Flanks]
                    Chromosome:
                    3:129316786 (GRCh38)
                    3:129035629 (GRCh37)
                    Canonical SPDI:
                    NC_000003.12:129316785:A:T
                    Gene:
                    H1-10 (Varview), H1-10-AS1 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000007/1 (GnomAD)
                    HGVS:
                    10.

                    rs1488815597 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      3:129316000 (GRCh38)
                      3:129034843 (GRCh37)
                      Canonical SPDI:
                      NC_000003.12:129315999:G:A
                      Gene:
                      H1-10 (Varview), H1-10-AS1 (Varview)
                      Functional Consequence:
                      2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      A=0./0 (ALFA)
                      HGVS:
                      11.

                      rs1488661297 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        3:129324268 (GRCh38)
                        3:129043111 (GRCh37)
                        Canonical SPDI:
                        NC_000003.12:129324267:T:C
                        Gene:
                        H1-10-AS1 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000007/1 (GnomAD)
                        HGVS:
                        12.

                        rs1488457348 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>G [Show Flanks]
                          Chromosome:
                          3:129316241 (GRCh38)
                          3:129035084 (GRCh37)
                          Canonical SPDI:
                          NC_000003.12:129316240:T:G
                          Gene:
                          H1-10 (Varview), H1-10-AS1 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000004/1 (TOPMED)
                          G=0.000007/1 (GnomAD)
                          G=0.000177/3 (TOMMO)
                          ...more
                          HGVS:
                          13.

                          rs1488442356 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            3:129323617 (GRCh38)
                            3:129042460 (GRCh37)
                            Canonical SPDI:
                            NC_000003.12:129323616:G:A
                            Gene:
                            H1-10-AS1 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000008/2 (TOPMED)
                            HGVS:
                            14.

                            rs1488031437 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              3:129323326 (GRCh38)
                              3:129042169 (GRCh37)
                              Canonical SPDI:
                              NC_000003.12:129323325:C:T
                              Gene:
                              H1-10-AS1 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000008/2 (TOPMED)
                              HGVS:
                              15.

                              rs1488002526 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                3:129322336 (GRCh38)
                                3:129041179 (GRCh37)
                                Canonical SPDI:
                                NC_000003.12:129322335:G:A
                                Gene:
                                H1-10-AS1 (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)
                                ...more
                                HGVS:
                                16.

                                rs1487980003 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  3:129316203 (GRCh38)
                                  3:129035046 (GRCh37)
                                  Canonical SPDI:
                                  NC_000003.12:129316202:G:A
                                  Gene:
                                  H1-10 (Varview), H1-10-AS1 (Varview)
                                  Functional Consequence:
                                  2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000023/6 (TOPMED)
                                  A=0.000029/4 (GnomAD)
                                  ...more
                                  HGVS:
                                  17.

                                  rs1487472236 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    3:129316081 (GRCh38)
                                    3:129034924 (GRCh37)
                                    Canonical SPDI:
                                    NC_000003.12:129316080:C:T
                                    Gene:
                                    H1-10 (Varview), H1-10-AS1 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.00003/2 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1486065004 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      CTATAT>- [Show Flanks]
                                      Chromosome:
                                      3:129322421 (GRCh38)
                                      3:129041264 (GRCh37)
                                      Canonical SPDI:
                                      NC_000003.12:129322409:TATATCTATATCTATAT:TATATCTATAT
                                      Gene:
                                      H1-10-AS1 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TATATCTATAT=0.000071/1 (ALFA)
                                      -=0.000004/1 (TOPMED)
                                      -=0.000015/2 (GnomAD)
                                      ...more
                                      HGVS:
                                      19.

                                      rs1485826039 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        3:129319476 (GRCh38)
                                        3:129038319 (GRCh37)
                                        Canonical SPDI:
                                        NC_000003.12:129319475:C:T
                                        Gene:
                                        H1-10-AS1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0.000142/2 (ALFA)
                                        T=0.000014/2 (GnomAD)
                                        T=0.000045/12 (TOPMED)
                                        ...more
                                        HGVS:
                                        20.

                                        rs1485454192 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>C [Show Flanks]
                                          Chromosome:
                                          3:129314849 (GRCh38)
                                          3:129033692 (GRCh37)
                                          Canonical SPDI:
                                          NC_000003.12:129314848:A:C
                                          Gene:
                                          H1-10 (Varview), H1-10-AS1 (Varview)
                                          Functional Consequence:
                                          upstream_transcript_variant,3_prime_UTR_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)
                                          ...more
                                          HGVS:

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...
                                          External link. Please review our privacy policy.