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1.

rs1491121147 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->GGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCACCGCGC,GGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAACGCGC,GGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,GGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,GGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,GGCTCGCGCTCCGCGC [Show Flanks]
    Chromosome:
    11:59106705 (GRCh38)
    11:58874179 (GRCh37)
    Canonical SPDI:
    NC_000011.10:59106705:CGCGC:CGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCACCGCGC,NC_000011.10:59106705:CGCGC:CGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAACGCGC,NC_000011.10:59106705:CGCGC:CGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,NC_000011.10:59106705:CGCGC:CGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,NC_000011.10:59106705:CGCGC:CGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCCCGCCAGCGCGCGGCTCGCGCTCCGCGC,NC_000011.10:59106705:CGCGC:CGCGCGGCTCGCGCTCCGCGC
    Gene:
    FAM111B (Varview), LOC105369315 (Varview)
    Functional Consequence:
    non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    CGCGCGGCTCGCGCTCCGCGC=0.00017/2 (ALFA)
    HGVS:
    NC_000011.10:g.59106706_59106710CGCGCGGCTCCCGCCAG[2]CG[3]GCTCCCGCCACCGCGC[1], NC_000011.10:g.59106706_59106710CGCGCGGCTCCCGCCAG[3]CG[3]GCTCCCGCCAACGCGC[1], NC_000011.10:g.59106706_59106710CGCGCGGCTCCCGCCAG[5]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.10:g.59106706_59106710CGCGCGGCTCCCGCCAG[4]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.10:g.59106706_59106710CGCGCGGCTCCCGCCAG[3]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.10:g.59106706_59106710CG[3]GCTCGCGCTCCGCGC[1], NC_000011.9:g.58874179_58874183CGCGCGGCTCCCGCCAG[2]CG[3]GCTCCCGCCACCGCGC[1], NC_000011.9:g.58874179_58874183CGCGCGGCTCCCGCCAG[3]CG[3]GCTCCCGCCAACGCGC[1], NC_000011.9:g.58874179_58874183CGCGCGGCTCCCGCCAG[5]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.9:g.58874179_58874183CGCGCGGCTCCCGCCAG[4]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.9:g.58874179_58874183CGCGCGGCTCCCGCCAG[3]CG[3]GCTCGCGCTCCGCGC[1], NC_000011.9:g.58874179_58874183CG[3]GCTCGCGCTCCGCGC[1], NG_034129.1:g.4522_4526CGCGCGGCTCCCGCCAG[2]CG[3]GCTCCCGCCACCGCGC[1], NG_034129.1:g.4522_4526CGCGCGGCTCCCGCCAG[3]CG[3]GCTCCCGCCAACGCGC[1], NG_034129.1:g.4522_4526CGCGCGGCTCCCGCCAG[5]CG[3]GCTCGCGCTCCGCGC[1], NG_034129.1:g.4522_4526CGCGCGGCTCCCGCCAG[4]CG[3]GCTCGCGCTCCGCGC[1], NG_034129.1:g.4522_4526CGCGCGGCTCCCGCCAG[3]CG[3]GCTCGCGCTCCGCGC[1], NG_034129.1:g.4522_4526CG[3]GCTCGCGCTCCGCGC[1], XR_001748221.3:n.16_20GC[2]GGTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_001748221.3:n.16_20GC[2]GTTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_001748221.3:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_001748221.3:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_001748221.3:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_001748221.3:n.16_20GC[2]GGAGCGCGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GGTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GTTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062680.1:n.16_20GC[2]GGAGCGCGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GGTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GTTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GGAGCGCGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCGCTGGCGGGAGCCGCGCG[1], XR_007062678.1:n.16_20GC[2]GGAGCGCGAGCCGCGCG[1]
    2.

    rs1490952261 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      11:59112289 (GRCh38)
      11:58879762 (GRCh37)
      Canonical SPDI:
      NC_000011.10:59112288:A:G
      Gene:
      FAM111B (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000014/2 (GnomAD)
      G=0.000019/5 (TOPMED)
      HGVS:
      3.

      rs1490926481 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>T [Show Flanks]
        Chromosome:
        11:59113443 (GRCh38)
        11:58880916 (GRCh37)
        Canonical SPDI:
        NC_000011.10:59113442:G:T
        Gene:
        FAM111B (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000019/5 (TOPMED)
        HGVS:
        4.

        rs1490746630 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>C,G [Show Flanks]
          Chromosome:
          11:59105788 (GRCh38)
          11:58873261 (GRCh37)
          Canonical SPDI:
          NC_000011.10:59105787:A:C,NC_000011.10:59105787:A:G
          Gene:
          FAM111B (Varview), LOC105369315 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0./0 (ALFA)
          C=0.000021/3 (GnomAD)
          C=0.00006/1 (TOMMO)
          HGVS:
          5.

          rs1490709731 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C,G [Show Flanks]
            Chromosome:
            11:59106560 (GRCh38)
            11:58874033 (GRCh37)
            Canonical SPDI:
            NC_000011.10:59106559:T:C,NC_000011.10:59106559:T:G
            Gene:
            FAM111B (Varview), LOC105369315 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            C=0.000007/1 (GnomAD)
            HGVS:
            6.

            rs1490581985 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              11:59105403 (GRCh38)
              11:58872876 (GRCh37)
              Canonical SPDI:
              NC_000011.10:59105402:C:T
              Gene:
              FAM111B (Varview), LOC105369315 (Varview)
              Functional Consequence:
              non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0./0 (ALFA)
              T=0.000008/2 (TOPMED)
              HGVS:
              7.

              rs1490551505 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                11:59106212 (GRCh38)
                11:58873685 (GRCh37)
                Canonical SPDI:
                NC_000011.10:59106211:C:T
                Gene:
                FAM111B (Varview), LOC105369315 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                T=0./0 (ALFA)
                HGVS:
                8.

                rs1490458260 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  11:59112178 (GRCh38)
                  11:58879651 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:59112177:T:C
                  Gene:
                  FAM111B (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000011/3 (TOPMED)
                  C=0.000014/2 (GnomAD)
                  HGVS:
                  9.

                  rs1490337886 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    11:59120188 (GRCh38)
                    11:58887661 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:59120187:A:G
                    Gene:
                    FAM111B (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0.000071/1 (ALFA)
                    G=0.000008/2 (TOPMED)
                    G=0.00006/1 (TOMMO)
                    HGVS:
                    10.

                    rs1489963371 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>C,T [Show Flanks]
                      Chromosome:
                      11:59111258 (GRCh38)
                      11:58878731 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:59111257:G:C,NC_000011.10:59111257:G:T
                      Gene:
                      FAM111B (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      C=0.000004/1 (TOPMED)
                      T=0.000007/1 (GnomAD)
                      HGVS:
                      11.

                      rs1489959175 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        AGCAT>- [Show Flanks]
                        Chromosome:
                        11:59112360 (GRCh38)
                        11:58879833 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:59112358:TAGCAT:T
                        Gene:
                        FAM111B (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        -=0.000011/3 (TOPMED)
                        HGVS:
                        12.

                        rs1489570836 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          CA>- [Show Flanks]
                          Chromosome:
                          11:59114385 (GRCh38)
                          11:58881858 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:59114383:ACA:A
                          Gene:
                          FAM111B (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          -=0.000004/1 (TOPMED)
                          -=0.000007/1 (GnomAD)
                          HGVS:
                          13.

                          rs1489555032 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            11:59105370 (GRCh38)
                            11:58872843 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:59105369:G:A
                            Gene:
                            FAM111B (Varview), LOC105369315 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0.0002/1 (ALFA)
                            HGVS:
                            14.

                            rs1489502745 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>G [Show Flanks]
                              Chromosome:
                              11:59106953 (GRCh38)
                              11:58874426 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:59106952:T:G
                              Gene:
                              FAM111B (Varview), LOC105369315 (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,upstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0.00025/3 (ALFA)
                              G=0.00055/1 (Korea1K)
                              HGVS:
                              15.

                              rs1489268972 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                11:59119054 (GRCh38)
                                11:58886527 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:59119053:C:T
                                Gene:
                                FAM111B (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000008/2 (TOPMED)
                                HGVS:
                                16.

                                rs1489246397 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  11:59127848 (GRCh38)
                                  11:58895321 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:59127847:G:C
                                  Gene:
                                  FAM111B (Varview)
                                  Functional Consequence:
                                  downstream_transcript_variant,500B_downstream_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000014/2 (GnomAD)
                                  HGVS:
                                  17.

                                  rs1489245899 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    11:59116457 (GRCh38)
                                    11:58883930 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:59116456:C:T
                                    Gene:
                                    FAM111B (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000007/1 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1489106432 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A,C [Show Flanks]
                                      Chromosome:
                                      11:59114777 (GRCh38)
                                      11:58882250 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:59114776:G:A,NC_000011.10:59114776:G:C
                                      Gene:
                                      FAM111B (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000011/3 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1489055798 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>G,T [Show Flanks]
                                        Chromosome:
                                        11:59115930 (GRCh38)
                                        11:58883403 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:59115929:C:G,NC_000011.10:59115929:C:T
                                        Gene:
                                        FAM111B (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        HGVS:
                                        20.

                                        rs1488790651 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          11:59114366 (GRCh38)
                                          11:58881839 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:59114365:G:A
                                          Gene:
                                          FAM111B (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)
                                          A=0.000566/9 (TOMMO)
                                          A=0.000685/2 (KOREAN)
                                          A=0.001092/2 (Korea1K)
                                          HGVS:

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