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Links from Nucleotide

Items: 1 to 20 of 103

1.

rs1480252637 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    13:21872814 (GRCh38)
    13:22446953 (GRCh37)
    Canonical SPDI:
    NC_000013.11:21872813:T:C
    Gene:
    LINC00424 (Varview)
    Functional Consequence:
    non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.000142/2 (ALFA)
    C=0.000014/2 (GnomAD)
    C=0.000023/6 (TOPMED)
    ...more
    HGVS:
    2.

    rs1479791863 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      13:21873206 (GRCh38)
      13:22447345 (GRCh37)
      Canonical SPDI:
      NC_000013.11:21873205:T:C
      Gene:
      LINC00424 (Varview)
      Functional Consequence:
      non_coding_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      C=0./0 (ALFA)
      C=0./0 (GnomAD)
      HGVS:
      3.

      rs1478873231 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        13:21873075 (GRCh38)
        13:22447214 (GRCh37)
        Canonical SPDI:
        NC_000013.11:21873074:C:T
        Gene:
        LINC00424 (Varview)
        Functional Consequence:
        non_coding_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000015/4 (TOPMED)
        HGVS:
        4.

        rs1471459211 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,T [Show Flanks]
          Chromosome:
          13:21873059 (GRCh38)
          13:22447198 (GRCh37)
          Canonical SPDI:
          NC_000013.11:21873058:G:A,NC_000013.11:21873058:G:T
          Gene:
          LINC00424 (Varview)
          Functional Consequence:
          non_coding_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (TOPMED)
          HGVS:
          5.

          rs1467376282 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>T [Show Flanks]
            Chromosome:
            13:21873186 (GRCh38)
            13:22447325 (GRCh37)
            Canonical SPDI:
            NC_000013.11:21873185:G:T
            Gene:
            LINC00424 (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)
            ...more
            HGVS:
            6.

            rs1466655039 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              13:21878156 (GRCh38)
              13:22452295 (GRCh37)
              Canonical SPDI:
              NC_000013.11:21878155:C:T
              Gene:
              LINC00424 (Varview)
              Functional Consequence:
              non_coding_transcript_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0./0 (ALFA)
              HGVS:
              7.

              rs1464337513 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                13:21873062 (GRCh38)
                13:22447201 (GRCh37)
                Canonical SPDI:
                NC_000013.11:21873061:G:A
                Gene:
                LINC00424 (Varview)
                Functional Consequence:
                non_coding_transcript_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                A=0.000004/1 (TOPMED)
                A=0.000014/2 (GnomAD)
                ...more
                HGVS:
                8.

                rs1456028071 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>C [Show Flanks]
                  Chromosome:
                  13:21872860 (GRCh38)
                  13:22446999 (GRCh37)
                  Canonical SPDI:
                  NC_000013.11:21872859:G:C
                  Gene:
                  LINC00424 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000007/1 (GnomAD)
                  HGVS:
                  9.

                  rs1423138636 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>A,C [Show Flanks]
                    Chromosome:
                    13:21873084 (GRCh38)
                    13:22447223 (GRCh37)
                    Canonical SPDI:
                    NC_000013.11:21873083:T:A,NC_000013.11:21873083:T:C
                    Gene:
                    LINC00424 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000004/1 (TOPMED)
                    A=0.00006/1 (TOMMO)
                    ...more
                    HGVS:
                    10.

                    rs1423101277 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,T [Show Flanks]
                      Chromosome:
                      13:21872991 (GRCh38)
                      13:22447130 (GRCh37)
                      Canonical SPDI:
                      NC_000013.11:21872990:G:A,NC_000013.11:21872990:G:T
                      Gene:
                      LINC00424 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      T=0.000007/1 (GnomAD)
                      HGVS:
                      11.

                      rs1420839102 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>C,T [Show Flanks]
                        Chromosome:
                        13:21872873 (GRCh38)
                        13:22447012 (GRCh37)
                        Canonical SPDI:
                        NC_000013.11:21872872:G:C,NC_000013.11:21872872:G:T
                        Gene:
                        LINC00424 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000008/2 (TOPMED)
                        C=0.000035/1 (TOMMO)
                        ...more
                        HGVS:
                        12.

                        rs1390415028 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>G [Show Flanks]
                          Chromosome:
                          13:21873149 (GRCh38)
                          13:22447288 (GRCh37)
                          Canonical SPDI:
                          NC_000013.11:21873148:T:G
                          Gene:
                          LINC00424 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant
                          Validated:
                          by frequency
                          MAF:
                          G=0.000007/1 (GnomAD)
                          HGVS:
                          13.

                          rs1386360612 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G [Show Flanks]
                            Chromosome:
                            13:21872888 (GRCh38)
                            13:22447027 (GRCh37)
                            Canonical SPDI:
                            NC_000013.11:21872887:C:G
                            Gene:
                            LINC00424 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000007/1 (GnomAD)
                            HGVS:
                            14.

                            rs1382635069 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>G [Show Flanks]
                              Chromosome:
                              13:21872875 (GRCh38)
                              13:22447014 (GRCh37)
                              Canonical SPDI:
                              NC_000013.11:21872874:T:G
                              Gene:
                              LINC00424 (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000011/3 (TOPMED)
                              G=0.000021/3 (GnomAD)
                              ...more
                              HGVS:
                              15.

                              rs1364688758 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>A,T [Show Flanks]
                                Chromosome:
                                13:21873030 (GRCh38)
                                13:22447169 (GRCh37)
                                Canonical SPDI:
                                NC_000013.11:21873029:C:A,NC_000013.11:21873029:C:T
                                Gene:
                                LINC00424 (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=0.000071/1 (TOMMO)
                                ...more
                                HGVS:
                                16.

                                rs1363032454 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ->CCTT [Show Flanks]
                                  Chromosome:
                                  13:21872960 (GRCh38)
                                  13:22447100 (GRCh37)
                                  Canonical SPDI:
                                  NC_000013.11:21872960:T:TCCTT
                                  Gene:
                                  LINC00424 (Varview)
                                  Functional Consequence:
                                  non_coding_transcript_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  TCCTT=0./0 (ALFA)
                                  TCCT=0.000008/2 (TOPMED)
                                  HGVS:
                                  17.

                                  rs1360070344 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A,T [Show Flanks]
                                    Chromosome:
                                    13:21873176 (GRCh38)
                                    13:22447315 (GRCh37)
                                    Canonical SPDI:
                                    NC_000013.11:21873175:G:A,NC_000013.11:21873175:G:T
                                    Gene:
                                    LINC00424 (Varview)
                                    Functional Consequence:
                                    non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0.000054/1 (ALFA)
                                    A=0.000015/4 (TOPMED)
                                    A=0.000071/1 (TOMMO)
                                    T=0.000223/1 (Estonian)
                                    ...more
                                    HGVS:
                                    18.

                                    rs1358049790 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      13:21872857 (GRCh38)
                                      13:22446996 (GRCh37)
                                      Canonical SPDI:
                                      NC_000013.11:21872856:C:T
                                      Gene:
                                      LINC00424 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0.000071/1 (ALFA)
                                      T=0.000004/1 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1348576233 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>A [Show Flanks]
                                        Chromosome:
                                        13:21872825 (GRCh38)
                                        13:22446964 (GRCh37)
                                        Canonical SPDI:
                                        NC_000013.11:21872824:T:A
                                        Gene:
                                        LINC00424 (Varview)
                                        Functional Consequence:
                                        non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        HGVS:
                                        20.

                                        rs1348236997 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>T [Show Flanks]
                                          Chromosome:
                                          13:21872937 (GRCh38)
                                          13:22447076 (GRCh37)
                                          Canonical SPDI:
                                          NC_000013.11:21872936:G:T
                                          Gene:
                                          LINC00424 (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0.000054/1 (ALFA)
                                          T=0.000004/1 (TOPMED)
                                          T=0.000007/1 (GnomAD)
                                          T=0.000223/1 (Estonian)
                                          ...more
                                          HGVS:

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