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1.

rs1491530280 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    AA>- [Show Flanks]
    Chromosome:
    9:86949511 (GRCh38)
    9:89564426 (GRCh37)
    Canonical SPDI:
    NC_000009.12:86949510:AA:
    Gene:
    GAS1RR (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    -=0./0 (ALFA)
    -=0.000004/1 (TOPMED)
    HGVS:
    2.

    rs1491238840 has merged into rs398068752 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTGTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      9:86948033 (GRCh38)
      9:89562948 (GRCh37)
      Canonical SPDI:
      NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000009.12:86948027:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      GAS1 (Varview), GAS1RR (Varview)
      Functional Consequence:
      upstream_transcript_variant,2KB_upstream_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTT=0./0 (ALFA)
      HGVS:
      NC_000009.12:g.86948033_86948042del, NC_000009.12:g.86948036_86948042del, NC_000009.12:g.86948037_86948042del, NC_000009.12:g.86948038_86948042del, NC_000009.12:g.86948039_86948042del, NC_000009.12:g.86948040_86948042del, NC_000009.12:g.86948041_86948042del, NC_000009.12:g.86948042del, NC_000009.12:g.86948042dup, NC_000009.12:g.86948041_86948042dup, NC_000009.12:g.86948040_86948042dup, NC_000009.12:g.86948028_86948042T[18]GTTTTTTTTTTTTTTT[1], NC_000009.12:g.86948039_86948042dup, NC_000009.12:g.86948038_86948042dup, NC_000009.12:g.86948037_86948042dup, NC_000009.12:g.86948028_86948042T[21]GTTTTTTTTTTTTTTTTTT[1], NC_000009.12:g.86948028_86948042T[21]GTTTTTTTTTTTTTTTTTTT[1], NC_000009.12:g.86948028_86948042T[21]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000009.12:g.86948036_86948042dup, NC_000009.12:g.86948035_86948042dup, NC_000009.12:g.86948034_86948042dup, NC_000009.12:g.86948033_86948042dup, NC_000009.12:g.86948032_86948042dup, NC_000009.12:g.86948030_86948042dup, NC_000009.12:g.86948029_86948042dup, NC_000009.12:g.86948028_86948042dup, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.12:g.86948042_86948043insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562948_89562957del, NC_000009.11:g.89562951_89562957del, NC_000009.11:g.89562952_89562957del, NC_000009.11:g.89562953_89562957del, NC_000009.11:g.89562954_89562957del, NC_000009.11:g.89562955_89562957del, NC_000009.11:g.89562956_89562957del, NC_000009.11:g.89562957del, NC_000009.11:g.89562957dup, NC_000009.11:g.89562956_89562957dup, NC_000009.11:g.89562955_89562957dup, NC_000009.11:g.89562943_89562957T[18]GTTTTTTTTTTTTTTT[1], NC_000009.11:g.89562954_89562957dup, NC_000009.11:g.89562953_89562957dup, NC_000009.11:g.89562952_89562957dup, NC_000009.11:g.89562943_89562957T[21]GTTTTTTTTTTTTTTTTTT[1], NC_000009.11:g.89562943_89562957T[21]GTTTTTTTTTTTTTTTTTTT[1], NC_000009.11:g.89562943_89562957T[21]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000009.11:g.89562951_89562957dup, NC_000009.11:g.89562950_89562957dup, NC_000009.11:g.89562949_89562957dup, NC_000009.11:g.89562948_89562957dup, NC_000009.11:g.89562947_89562957dup, NC_000009.11:g.89562945_89562957dup, NC_000009.11:g.89562944_89562957dup, NC_000009.11:g.89562943_89562957dup, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000009.11:g.89562957_89562958insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032760.1:g.4153_4162del, NG_032760.1:g.4156_4162del, NG_032760.1:g.4157_4162del, NG_032760.1:g.4158_4162del, NG_032760.1:g.4159_4162del, NG_032760.1:g.4160_4162del, NG_032760.1:g.4161_4162del, NG_032760.1:g.4162del, NG_032760.1:g.4162dup, NG_032760.1:g.4161_4162dup, NG_032760.1:g.4160_4162dup, NG_032760.1:g.4148_4162A[15]CAAAAAAAAAAAAAAAAAA[1], NG_032760.1:g.4159_4162dup, NG_032760.1:g.4158_4162dup, NG_032760.1:g.4157_4162dup, NG_032760.1:g.4148_4162A[18]CAAAAAAAAAAAAAAAAAAAAA[1], NG_032760.1:g.4148_4162A[19]CAAAAAAAAAAAAAAAAAAAAA[1], NG_032760.1:g.4148_4162A[30]CAAAAAAAAAAAAAAAAAAAAA[1], NG_032760.1:g.4156_4162dup, NG_032760.1:g.4155_4162dup, NG_032760.1:g.4154_4162dup, NG_032760.1:g.4153_4162dup, NG_032760.1:g.4152_4162dup, NG_032760.1:g.4150_4162dup, NG_032760.1:g.4149_4162dup, NG_032760.1:g.4148_4162dup, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_032760.1:g.4162_4163insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
      3.

      rs1491232746 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ->CA [Show Flanks]
        Chromosome:
        9:86949511 (GRCh38)
        9:89564427 (GRCh37)
        Canonical SPDI:
        NC_000009.12:86949511:ACA:ACACA
        Gene:
        GAS1RR (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        ACACA=0./0 (ALFA)
        HGVS:
        4.

        rs1490689325 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>G,T [Show Flanks]
          Chromosome:
          9:86947017 (GRCh38)
          9:89561932 (GRCh37)
          Canonical SPDI:
          NC_000009.12:86947016:C:G,NC_000009.12:86947016:C:T
          Gene:
          GAS1 (Varview), GAS1RR (Varview)
          Functional Consequence:
          5_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          G=0.000007/1 (GnomAD)
          G=0.000008/2 (TOPMED)
          HGVS:
          5.

          rs1489554184 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C,G [Show Flanks]
            Chromosome:
            9:86946885 (GRCh38)
            9:89561800 (GRCh37)
            Canonical SPDI:
            NC_000009.12:86946884:T:C,NC_000009.12:86946884:T:G
            Gene:
            GAS1 (Varview), GAS1RR (Varview)
            Functional Consequence:
            5_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0.00022/1 (ALFA)
            G=0.00007/1 (TOMMO)
            C=0.00022/1 (Estonian)
            HGVS:
            6.

            rs1489402492 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>A [Show Flanks]
              Chromosome:
              9:86945842 (GRCh38)
              9:89560757 (GRCh37)
              Canonical SPDI:
              NC_000009.12:86945841:G:A
              Gene:
              GAS1 (Varview)
              Functional Consequence:
              coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa
              MAF:
              A=0./0 (ALFA)
              A=0.00001/1 (GnomAD_exomes)
              HGVS:
              7.

              rs1489370929 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                9:86946440 (GRCh38)
                9:89561355 (GRCh37)
                Canonical SPDI:
                NC_000009.12:86946439:T:C
                Gene:
                GAS1 (Varview)
                Functional Consequence:
                coding_sequence_variant,missense_variant
                HGVS:
                8.

                rs1489092243 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  A>-,AA [Show Flanks]
                  Chromosome:
                  9:86951932 (GRCh38)
                  9:89566847 (GRCh37)
                  Canonical SPDI:
                  NC_000009.12:86951931:AAAAAA:AAAAA,NC_000009.12:86951931:AAAAAA:AAAAAAA
                  Gene:
                  GAS1RR (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAA=0./0 (ALFA)
                  -=0.000034/9 (TOPMED)
                  HGVS:
                  9.

                  rs1488720138 has merged into rs907485406 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    GGGCCGCCCGCGCCG>-,GGGCCGCCCGCGCCGGGGCCGCCCGCGCCG [Show Flanks]
                    Chromosome:
                    9:86946307 (GRCh38)
                    9:89561222 (GRCh37)
                    Canonical SPDI:
                    NC_000009.12:86946294:CCGCCCGCGCCGGGGCCGCCCGCGCCG:CCGCCCGCGCCG,NC_000009.12:86946294:CCGCCCGCGCCGGGGCCGCCCGCGCCG:CCGCCCGCGCCGGGGCCGCCCGCGCCGGGGCCGCCCGCGCCG
                    Gene:
                    GAS1 (Varview)
                    Functional Consequence:
                    inframe_deletion,coding_sequence_variant,inframe_insertion
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    CCGCCCGCGCCGGGGCCGCCCGCGCCGGGGCCGCCCGCGCCG=0./0 (ALFA)
                    -=0.00004/3 (GnomAD_exomes)
                    -=0.00016/1 (1000Genomes)
                    CCGCCCGCGCCGGGG=0.00057/1 (Korea1K)
                    HGVS:
                    10.

                    rs1488697484 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>A,G [Show Flanks]
                      Chromosome:
                      9:86948269 (GRCh38)
                      9:89563184 (GRCh37)
                      Canonical SPDI:
                      NC_000009.12:86948268:C:A,NC_000009.12:86948268:C:G
                      Gene:
                      GAS1 (Varview), GAS1RR (Varview)
                      Functional Consequence:
                      upstream_transcript_variant,2KB_upstream_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      G=0./0 (ALFA)
                      HGVS:
                      11.

                      rs1488506493 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        G>- [Show Flanks]
                        Chromosome:
                        9:86942385 (GRCh38)
                        9:89557300 (GRCh37)
                        Canonical SPDI:
                        NC_000009.12:86942384:GG:G
                        Validated:
                        by frequency,by alfa
                        MAF:
                        GG=0./0 (ALFA)
                        -=0.000004/1 (TOPMED)
                        HGVS:
                        12.

                        rs1488477851 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,T [Show Flanks]
                          Chromosome:
                          9:86947091 (GRCh38)
                          9:89562006 (GRCh37)
                          Canonical SPDI:
                          NC_000009.12:86947090:G:A,NC_000009.12:86947090:G:T
                          Gene:
                          GAS1 (Varview), GAS1RR (Varview)
                          Functional Consequence:
                          5_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          HGVS:
                          13.

                          rs1488388762 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G,T [Show Flanks]
                            Chromosome:
                            9:86946770 (GRCh38)
                            9:89561685 (GRCh37)
                            Canonical SPDI:
                            NC_000009.12:86946769:C:G,NC_000009.12:86946769:C:T
                            Gene:
                            GAS1 (Varview), GAS1RR (Varview)
                            Functional Consequence:
                            coding_sequence_variant,upstream_transcript_variant,missense_variant,2KB_upstream_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000036/5 (GnomAD)
                            HGVS:
                            14.

                            rs1487889851 [Homo sapiens]
                              Variant type:
                              SNV:
                              Alleles:
                              ->CGGCG
                              Chromosome:
                              no mapping
                              Canonical SPDI:
                              15.

                              rs1487738496 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                9:86946141 (GRCh38)
                                9:89561056 (GRCh37)
                                Canonical SPDI:
                                NC_000009.12:86946140:C:T
                                Gene:
                                GAS1 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,missense_variant
                                Validated:
                                by frequency
                                MAF:
                                T=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                16.

                                rs1487725034 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>G [Show Flanks]
                                  Chromosome:
                                  9:86947731 (GRCh38)
                                  9:89562646 (GRCh37)
                                  Canonical SPDI:
                                  NC_000009.12:86947730:C:G
                                  Gene:
                                  GAS1 (Varview), GAS1RR (Varview)
                                  Functional Consequence:
                                  upstream_transcript_variant,2KB_upstream_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0.000108/2 (ALFA)
                                  G=0.000026/7 (TOPMED)
                                  G=0.000051/7 (GnomAD)
                                  G=0.000446/2 (Estonian)
                                  HGVS:
                                  17.

                                  rs1487634769 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A,C [Show Flanks]
                                    Chromosome:
                                    9:86946375 (GRCh38)
                                    9:89561290 (GRCh37)
                                    Canonical SPDI:
                                    NC_000009.12:86946374:G:A,NC_000009.12:86946374:G:C
                                    Gene:
                                    GAS1 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,synonymous_variant,missense_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.

                                    rs1487002578 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      9:86947505 (GRCh38)
                                      9:89562420 (GRCh37)
                                      Canonical SPDI:
                                      NC_000009.12:86947504:C:G
                                      Gene:
                                      GAS1 (Varview), GAS1RR (Varview)
                                      Functional Consequence:
                                      5_prime_UTR_variant,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:
                                      19.

                                      rs1486903504 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>T [Show Flanks]
                                        Chromosome:
                                        9:86951801 (GRCh38)
                                        9:89566716 (GRCh37)
                                        Canonical SPDI:
                                        NC_000009.12:86951800:G:T
                                        Gene:
                                        GAS1RR (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000004/1 (TOPMED)
                                        T=0.000007/1 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1486733551 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>C,T [Show Flanks]
                                          Chromosome:
                                          9:86949021 (GRCh38)
                                          9:89563936 (GRCh37)
                                          Canonical SPDI:
                                          NC_000009.12:86949020:G:C,NC_000009.12:86949020:G:T
                                          Gene:
                                          GAS1 (Varview), GAS1RR (Varview)
                                          Functional Consequence:
                                          upstream_transcript_variant,intron_variant,2KB_upstream_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0.000007/1 (GnomAD)
                                          HGVS:

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