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Items: 1 to 20 of 1257

1.

rs1491439024 has merged into rs3076135 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AG>-,AGAG,AGAGAG [Show Flanks]
    Chromosome:
    6:79234386 (GRCh38)
    6:79944103 (GRCh37)
    Canonical SPDI:
    NC_000006.12:79234379:AGAGAGAG:AGAGAG,NC_000006.12:79234379:AGAGAGAG:AGAGAGAGAG,NC_000006.12:79234379:AGAGAGAG:AGAGAGAGAGAG
    Gene:
    HMGN3 (Varview), HMGN3-AS1 (Varview)
    Functional Consequence:
    non_coding_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AGAGAGAGAGAG=0./0 (ALFA)
    AG=0./0 (GENOME_DK)
    AG=0./0 (Korea1K)
    -=0.000008/2 (TOPMED)
    AG=0.03006/30 (GoNL)
    AG=0.036066/139 (ALSPAC)
    AG=0.037723/169 (Estonian)
    AG=0.038026/141 (TWINSUK)
    AG=0.06/36 (NorthernSweden)
    AG=0.084465/423 (1000Genomes)
    AG=0.99994/16759 (TOMMO)
    HGVS:
    2.

    rs1490586254 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      G>- [Show Flanks]
      Chromosome:
      6:79235913 (GRCh38)
      6:79945630 (GRCh37)
      Canonical SPDI:
      NC_000006.12:79235912:G:
      Gene:
      HMGN3 (Varview), HMGN3-AS1 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0./0 (ALFA)
      -=0.000008/2 (TOPMED)
      HGVS:
      3.

      rs1490570061 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>G [Show Flanks]
        Chromosome:
        6:79237236 (GRCh38)
        6:79946953 (GRCh37)
        Canonical SPDI:
        NC_000006.12:79237235:T:G
        Gene:
        HMGN3-AS1 (Varview)
        Functional Consequence:
        downstream_transcript_variant,500B_downstream_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        G=0.000004/1 (TOPMED)
        G=0.000007/1 (GnomAD)
        HGVS:
        4.

        rs1489290644 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>A [Show Flanks]
          Chromosome:
          6:79237030 (GRCh38)
          6:79946747 (GRCh37)
          Canonical SPDI:
          NC_000006.12:79237029:C:A
          Gene:
          HMGN3-AS1 (Varview)
          Functional Consequence:
          downstream_transcript_variant,500B_downstream_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          A=0.000023/6 (TOPMED)
          HGVS:
          5.

          rs1488146281 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>G [Show Flanks]
            Chromosome:
            6:79234434 (GRCh38)
            6:79944151 (GRCh37)
            Canonical SPDI:
            NC_000006.12:79234433:T:G
            Gene:
            HMGN3 (Varview), HMGN3-AS1 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            G=0.000007/1 (GnomAD)
            HGVS:
            6.

            rs1486898833 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>T [Show Flanks]
              Chromosome:
              6:79235795 (GRCh38)
              6:79945512 (GRCh37)
              Canonical SPDI:
              NC_000006.12:79235794:A:T
              Gene:
              HMGN3 (Varview), HMGN3-AS1 (Varview)
              Functional Consequence:
              2KB_upstream_variant,upstream_transcript_variant,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:
              7.

              rs1486210566 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A,T [Show Flanks]
                Chromosome:
                6:79232601 (GRCh38)
                6:79942318 (GRCh37)
                Canonical SPDI:
                NC_000006.12:79232600:G:A,NC_000006.12:79232600:G:T
                Gene:
                HMGN3 (Varview), HMGN3-AS1 (Varview)
                Functional Consequence:
                2KB_upstream_variant,upstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0.000055/1 (ALFA)
                T=0.000008/2 (TOPMED)
                HGVS:
                8.

                rs1484968676 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>T [Show Flanks]
                  Chromosome:
                  6:79233409 (GRCh38)
                  6:79943126 (GRCh37)
                  Canonical SPDI:
                  NC_000006.12:79233408:A:T
                  Gene:
                  HMGN3 (Varview), HMGN3-AS1 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,upstream_transcript_variant,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:
                  9.

                  rs1484951245 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>G [Show Flanks]
                    Chromosome:
                    6:79237132 (GRCh38)
                    6:79946849 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:79237131:T:G
                    Gene:
                    HMGN3-AS1 (Varview)
                    Functional Consequence:
                    downstream_transcript_variant,500B_downstream_variant
                    Validated:
                    by frequency
                    MAF:
                    G=0.000007/1 (GnomAD)
                    HGVS:
                    10.

                    rs1484825668 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      6:79234124 (GRCh38)
                      6:79943841 (GRCh37)
                      Canonical SPDI:
                      NC_000006.12:79234123:T:C
                      Gene:
                      HMGN3 (Varview), HMGN3-AS1 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000007/1 (GnomAD)
                      C=0.000015/4 (TOPMED)
                      HGVS:
                      11.

                      rs1484508547 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        A>- [Show Flanks]
                        Chromosome:
                        6:79235669 (GRCh38)
                        6:79945386 (GRCh37)
                        Canonical SPDI:
                        NC_000006.12:79235668:AA:A
                        Gene:
                        HMGN3 (Varview), HMGN3-AS1 (Varview)
                        Functional Consequence:
                        2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        AA=0./0 (ALFA)
                        HGVS:
                        12.
                        13.

                        rs1484259825 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          6:79235968 (GRCh38)
                          6:79945685 (GRCh37)
                          Canonical SPDI:
                          NC_000006.12:79235967:T:C
                          Gene:
                          HMGN3 (Varview), HMGN3-AS1 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000004/1 (TOPMED)
                          C=0.000014/2 (GnomAD)
                          HGVS:
                          14.

                          rs1483989235 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            6:79233841 (GRCh38)
                            6:79943558 (GRCh37)
                            Canonical SPDI:
                            NC_000006.12:79233840:C:T
                            Gene:
                            HMGN3 (Varview), HMGN3-AS1 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000021/3 (GnomAD)
                            T=0.000023/6 (TOPMED)
                            HGVS:
                            15.

                            rs1483859115 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>G [Show Flanks]
                              Chromosome:
                              6:79234523 (GRCh38)
                              6:79944240 (GRCh37)
                              Canonical SPDI:
                              NC_000006.12:79234522:A:G
                              Gene:
                              HMGN3 (Varview), HMGN3-AS1 (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000004/1 (TOPMED)
                              G=0.000007/1 (GnomAD)
                              HGVS:
                              16.

                              rs1483759400 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                A>- [Show Flanks]
                                Chromosome:
                                6:79231715 (GRCh38)
                                6:79941432 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:79231714:A:
                                Gene:
                                HMGN3 (Varview), HMGN3-AS1 (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,upstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                -=0./0 (ALFA)
                                -=0.000014/2 (GnomAD)
                                HGVS:
                                17.

                                rs1483750099 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  6:79233997 (GRCh38)
                                  6:79943714 (GRCh37)
                                  Canonical SPDI:
                                  NC_000006.12:79233996:G:C
                                  Gene:
                                  HMGN3 (Varview), HMGN3-AS1 (Varview)
                                  Functional Consequence:
                                  intron_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.
                                  20.

                                  rs1482877144 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A,T [Show Flanks]
                                    Chromosome:
                                    6:79234852 (GRCh38)
                                    6:79944569 (GRCh37)
                                    Canonical SPDI:
                                    NC_000006.12:79234851:C:A,NC_000006.12:79234851:C:T
                                    Gene:
                                    HMGN3 (Varview), HMGN3-AS1 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    A=0.00004/1 (TOMMO)
                                    HGVS:

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