U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 917

1.

rs1491093943 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    GA>- [Show Flanks]
    Chromosome:
    4:3587974 (GRCh38)
    4:3589701 (GRCh37)
    Canonical SPDI:
    NC_000004.12:3587972:AGA:A
    Gene:
    LINC00955 (Varview)
    Functional Consequence:
    non_coding_transcript_variant
    Validated:
    by frequency,by cluster
    MAF:
    -=0.00025/4 (ExAC)
    HGVS:
    2.

    rs1486124153 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      4:3576996 (GRCh38)
      4:3578723 (GRCh37)
      Canonical SPDI:
      NC_000004.12:3576995:A:G
      Gene:
      LINC00955 (Varview)
      Functional Consequence:
      non_coding_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      G=0./0 (ALFA)
      G=0.000004/1 (TOPMED)
      HGVS:
      3.

      rs1485427449 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>G,T [Show Flanks]
        Chromosome:
        4:3590409 (GRCh38)
        4:3592136 (GRCh37)
        Canonical SPDI:
        NC_000004.12:3590408:C:G,NC_000004.12:3590408:C:T
        Gene:
        LINC00955 (Varview)
        Functional Consequence:
        non_coding_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0./0 (ALFA)
        G=0.000004/1 (TOPMED)
        HGVS:
        4.

        rs1485075196 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>A,G [Show Flanks]
          Chromosome:
          4:3590088 (GRCh38)
          4:3591815 (GRCh37)
          Canonical SPDI:
          NC_000004.12:3590087:C:A,NC_000004.12:3590087:C:G
          Gene:
          LINC00955 (Varview)
          Functional Consequence:
          non_coding_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0./0 (ALFA)
          G=0.000004/1 (TOPMED)
          A=0.000342/1 (KOREAN)
          HGVS:
          5.

          rs1485061712 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>T [Show Flanks]
            Chromosome:
            4:3589119 (GRCh38)
            4:3590846 (GRCh37)
            Canonical SPDI:
            NC_000004.12:3589118:A:T
            Gene:
            LINC00955 (Varview)
            Functional Consequence:
            non_coding_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            T=0./0 (GnomAD)
            HGVS:
            6.

            rs1484718039 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G,T [Show Flanks]
              Chromosome:
              4:3589923 (GRCh38)
              4:3591650 (GRCh37)
              Canonical SPDI:
              NC_000004.12:3589922:C:G,NC_000004.12:3589922:C:T
              Gene:
              LINC00955 (Varview)
              Functional Consequence:
              non_coding_transcript_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0./0 (ALFA)
              G=0.00034/1 (KOREAN)
              HGVS:
              7.

              rs1484692203 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                4:3589356 (GRCh38)
                4:3591083 (GRCh37)
                Canonical SPDI:
                NC_000004.12:3589355:G:A
                Gene:
                LINC00955 (Varview)
                Functional Consequence:
                non_coding_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                A=0./0 (ALFA)
                HGVS:
                8.

                rs1484548759 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  4:3576977 (GRCh38)
                  4:3578704 (GRCh37)
                  Canonical SPDI:
                  NC_000004.12:3576976:A:G
                  Gene:
                  LINC00955 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000015/4 (TOPMED)
                  HGVS:
                  9.

                  rs1484208555 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C [Show Flanks]
                    Chromosome:
                    4:3589312 (GRCh38)
                    4:3591039 (GRCh37)
                    Canonical SPDI:
                    NC_000004.12:3589311:T:C
                    Gene:
                    LINC00955 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant
                    HGVS:
                    10.

                    rs1484080755 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>T [Show Flanks]
                      Chromosome:
                      4:3590272 (GRCh38)
                      4:3591999 (GRCh37)
                      Canonical SPDI:
                      NC_000004.12:3590271:G:T
                      Gene:
                      LINC00955 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      T=0.0002/1 (ALFA)
                      T=0.0002/1 (Estonian)
                      HGVS:
                      11.

                      rs1483717586 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>C [Show Flanks]
                        Chromosome:
                        4:3589159 (GRCh38)
                        4:3590886 (GRCh37)
                        Canonical SPDI:
                        NC_000004.12:3589158:G:C
                        Gene:
                        LINC00955 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant
                        HGVS:
                        12.

                        rs1483100476 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          4:3590797 (GRCh38)
                          4:3592524 (GRCh37)
                          Canonical SPDI:
                          NC_000004.12:3590796:C:T
                          Gene:
                          LINC00955 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000021/3 (GnomAD)
                          T=0.00003/8 (TOPMED)
                          HGVS:
                          13.

                          rs1482911779 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            4:3590901 (GRCh38)
                            4:3592628 (GRCh37)
                            Canonical SPDI:
                            NC_000004.12:3590900:T:C
                            Gene:
                            LINC00955 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000007/1 (GnomAD)
                            C=0.000008/2 (TOPMED)
                            HGVS:
                            14.

                            rs1482734548 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>G [Show Flanks]
                              Chromosome:
                              4:3588938 (GRCh38)
                              4:3590665 (GRCh37)
                              Canonical SPDI:
                              NC_000004.12:3588937:T:G
                              Gene:
                              LINC00955 (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0.000071/1 (ALFA)
                              G=0.000007/1 (GnomAD)
                              G=0.000008/2 (TOPMED)
                              HGVS:
                              15.

                              rs1482185847 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>T [Show Flanks]
                                Chromosome:
                                4:3589049 (GRCh38)
                                4:3590776 (GRCh37)
                                Canonical SPDI:
                                NC_000004.12:3589048:A:T
                                Gene:
                                LINC00955 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                T=0.000007/1 (GnomAD)
                                HGVS:
                                16.

                                rs1479923237 [Homo sapiens]
                                  Variant type:
                                  SNV:
                                  Alleles:
                                  C>T
                                  Chromosome:
                                  no mapping
                                  Canonical SPDI:
                                  17.

                                  rs1479450828 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>G,T [Show Flanks]
                                    Chromosome:
                                    4:3589196 (GRCh38)
                                    4:3590923 (GRCh37)
                                    Canonical SPDI:
                                    NC_000004.12:3589195:C:G,NC_000004.12:3589195:C:T
                                    Gene:
                                    LINC00955 (Varview)
                                    Functional Consequence:
                                    non_coding_transcript_variant
                                    Validated:
                                    by cluster
                                    HGVS:
                                    18.

                                    rs1479339765 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      4:3587907 (GRCh38)
                                      4:3589634 (GRCh37)
                                      Canonical SPDI:
                                      NC_000004.12:3587906:T:C
                                      Gene:
                                      LINC00955 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0.000071/1 (ALFA)
                                      C=0.00003/8 (TOPMED)
                                      C=0.000051/7 (GnomAD)
                                      HGVS:
                                      19.

                                      rs1478834478 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        4:3590780 (GRCh38)
                                        4:3592507 (GRCh37)
                                        Canonical SPDI:
                                        NC_000004.12:3590779:A:G
                                        Gene:
                                        LINC00955 (Varview)
                                        Functional Consequence:
                                        non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0.000071/1 (ALFA)
                                        G=0.000007/1 (GnomAD)
                                        G=0.000011/3 (TOPMED)
                                        HGVS:
                                        20.

                                        rs1478733024 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A,T [Show Flanks]
                                          Chromosome:
                                          4:3590539 (GRCh38)
                                          4:3592266 (GRCh37)
                                          Canonical SPDI:
                                          NC_000004.12:3590538:G:A,NC_000004.12:3590538:G:T
                                          Gene:
                                          LINC00955 (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0.000071/1 (ALFA)
                                          T=0.000004/1 (TOPMED)
                                          HGVS:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...