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Items: 1 to 20 of 475

1.

rs781453944 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    1:206770334 (GRCh38)
    1:206943679 (GRCh37)
    Canonical SPDI:
    NC_000001.11:206770333:T:C
    Gene:
    IL10 (Varview), IL19 (Varview)
    Functional Consequence:
    intron_variant,upstream_transcript_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0./0 (ALFA)
    C=0./0 (ALSPAC)
    C=0.000014/2 (GnomAD)
    C=0.000015/4 (TOPMED)
    C=0.000539/2 (TWINSUK)
    HGVS:
    2.

    rs781288395 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      1:206769788 (GRCh38)
      1:206943133 (GRCh37)
      Canonical SPDI:
      NC_000001.11:206769787:G:A
      Gene:
      IL10 (Varview), IL19 (Varview)
      Functional Consequence:
      intron_variant,upstream_transcript_variant,2KB_upstream_variant
      Validated:
      by frequency,by cluster
      MAF:
      A=0.000016/2 (ExAC)
      A=0.000016/4 (GnomAD_exomes)
      HGVS:
      3.

      rs780746069 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C,G [Show Flanks]
        Chromosome:
        1:206771318 (GRCh38)
        1:206944663 (GRCh37)
        Canonical SPDI:
        NC_000001.11:206771317:T:C,NC_000001.11:206771317:T:G
        Gene:
        IL10 (Varview), IL19 (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        C=0./0 (ALFA)
        G=0.000007/1 (GnomAD)
        C=0.000008/1 (ExAC)
        C=0.000008/2 (TOPMED)
        HGVS:
        4.

        rs780612967 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          1:206771011 (GRCh38)
          1:206944356 (GRCh37)
          Canonical SPDI:
          NC_000001.11:206771010:C:T
          Gene:
          IL10 (Varview), IL19 (Varview)
          Functional Consequence:
          missense_variant,coding_sequence_variant,non_coding_transcript_variant,upstream_transcript_variant,intron_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
          Clinical significance:
          uncertain-significance
          Validated:
          by frequency,by cluster
          MAF:
          T=0.000008/1 (ExAC)
          T=0.000008/2 (GnomAD_exomes)
          HGVS:
          5.

          rs780388936 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A,G [Show Flanks]
            Chromosome:
            1:206769803 (GRCh38)
            1:206943148 (GRCh37)
            Canonical SPDI:
            NC_000001.11:206769802:C:A,NC_000001.11:206769802:C:G
            Gene:
            IL10 (Varview), IL19 (Varview)
            Functional Consequence:
            intron_variant,upstream_transcript_variant,2KB_upstream_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.00002/5 (GnomAD_exomes)
            G=0.000033/4 (ExAC)
            HGVS:
            6.

            rs780213087 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              1:206772388 (GRCh38)
              1:206945733 (GRCh37)
              Canonical SPDI:
              NC_000001.11:206772387:C:T
              Gene:
              IL10 (Varview), IL19 (Varview)
              Functional Consequence:
              coding_sequence_variant,non_coding_transcript_variant,upstream_transcript_variant,intron_variant,synonymous_variant,genic_upstream_transcript_variant
              Clinical significance:
              likely-benign
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0.000007/1 (GnomAD)
              T=0.00002/5 (GnomAD_exomes)
              T=0.00003/8 (TOPMED)
              T=0.000033/4 (ExAC)
              HGVS:
              7.

              rs780184268 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>A [Show Flanks]
                Chromosome:
                1:206773936 (GRCh38)
                1:206947281 (GRCh37)
                Canonical SPDI:
                NC_000001.11:206773935:C:A
                Gene:
                IL10 (Varview), IL19 (Varview)
                Functional Consequence:
                upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                A=0.000008/2 (TOPMED)
                HGVS:
                8.

                rs780158047 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  1:206768112 (GRCh38)
                  1:206941457 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:206768111:A:G
                  Gene:
                  IL10 (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant,non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0.000265/5 (ALFA)
                  G=0.000223/1 (Estonian)
                  G=0.000257/36 (GnomAD)
                  G=0.00027/1 (TWINSUK)
                  G=0.000283/75 (TOPMED)
                  G=0.001038/4 (ALSPAC)
                  G=0.001667/1 (NorthernSweden)
                  HGVS:
                  9.

                  rs780046311 has merged into rs2234662 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    GTGTGTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
                    Chromosome:
                    1:206773606 (GRCh38)
                    1:206946951 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:206773586:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                    Gene:
                    IL10 (Varview), IL19 (Varview)
                    Functional Consequence:
                    genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    TGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
                    -=0.4982/2495 (1000Genomes)
                    HGVS:
                    NC_000001.11:g.206773588GT[9], NC_000001.11:g.206773588GT[10], NC_000001.11:g.206773588GT[11], NC_000001.11:g.206773588GT[12], NC_000001.11:g.206773588GT[13], NC_000001.11:g.206773588GT[14], NC_000001.11:g.206773588GT[15], NC_000001.11:g.206773588GT[16], NC_000001.11:g.206773588GT[17], NC_000001.11:g.206773588GT[18], NC_000001.11:g.206773588GT[19], NC_000001.11:g.206773588GT[20], NC_000001.11:g.206773588GT[21], NC_000001.11:g.206773588GT[23], NC_000001.11:g.206773588GT[24], NC_000001.11:g.206773588GT[25], NC_000001.11:g.206773588GT[26], NC_000001.11:g.206773588GT[27], NC_000001.11:g.206773588GT[28], NC_000001.11:g.206773588GT[29], NC_000001.11:g.206773588GT[30], NC_000001.11:g.206773588GT[31], NC_000001.11:g.206773588GT[32], NC_000001.10:g.206946933GT[9], NC_000001.10:g.206946933GT[10], NC_000001.10:g.206946933GT[11], NC_000001.10:g.206946933GT[12], NC_000001.10:g.206946933GT[13], NC_000001.10:g.206946933GT[14], NC_000001.10:g.206946933GT[15], NC_000001.10:g.206946933GT[16], NC_000001.10:g.206946933GT[17], NC_000001.10:g.206946933GT[18], NC_000001.10:g.206946933GT[19], NC_000001.10:g.206946933GT[20], NC_000001.10:g.206946933GT[21], NC_000001.10:g.206946933GT[23], NC_000001.10:g.206946933GT[24], NC_000001.10:g.206946933GT[25], NC_000001.10:g.206946933GT[26], NC_000001.10:g.206946933GT[27], NC_000001.10:g.206946933GT[28], NC_000001.10:g.206946933GT[29], NC_000001.10:g.206946933GT[30], NC_000001.10:g.206946933GT[31], NC_000001.10:g.206946933GT[32], NG_012088.1:g.3865CA[9], NG_012088.1:g.3865CA[10], NG_012088.1:g.3865CA[11], NG_012088.1:g.3865CA[12], NG_012088.1:g.3865CA[13], NG_012088.1:g.3865CA[14], NG_012088.1:g.3865CA[15], NG_012088.1:g.3865CA[16], NG_012088.1:g.3865CA[17], NG_012088.1:g.3865CA[18], NG_012088.1:g.3865CA[19], NG_012088.1:g.3865CA[20], NG_012088.1:g.3865CA[21], NG_012088.1:g.3865CA[23], NG_012088.1:g.3865CA[24], NG_012088.1:g.3865CA[25], NG_012088.1:g.3865CA[26], NG_012088.1:g.3865CA[27], NG_012088.1:g.3865CA[28], NG_012088.1:g.3865CA[29], NG_012088.1:g.3865CA[30], NG_012088.1:g.3865CA[31], NG_012088.1:g.3865CA[32]
                    10.

                    rs779987907 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,C [Show Flanks]
                      Chromosome:
                      1:206771342 (GRCh38)
                      1:206944687 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:206771341:G:A,NC_000001.11:206771341:G:C
                      Gene:
                      IL10 (Varview), IL19 (Varview)
                      Functional Consequence:
                      intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      A=0.000008/2 (GnomAD_exomes)
                      A=0.000017/2 (ExAC)
                      HGVS:
                      11.

                      rs779792087 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>T [Show Flanks]
                        Chromosome:
                        1:206771512 (GRCh38)
                        1:206944857 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:206771511:A:T
                        Gene:
                        IL10 (Varview), IL19 (Varview)
                        Functional Consequence:
                        genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.00006/1 (TOMMO)
                        T=0.00026/1 (ALSPAC)
                        T=0.00027/1 (TWINSUK)
                        T=0.00068/2 (KOREAN)
                        HGVS:
                        12.

                        rs779067449 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>C [Show Flanks]
                          Chromosome:
                          1:206774383 (GRCh38)
                          1:206947728 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:206774382:G:C
                          Gene:
                          IL10 (Varview), IL19 (Varview)
                          Functional Consequence:
                          genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
                          Validated:
                          by cluster
                          HGVS:
                          13.

                          rs778676952 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>G [Show Flanks]
                            Chromosome:
                            1:206772267 (GRCh38)
                            1:206945612 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:206772266:T:G
                            Gene:
                            IL10 (Varview), IL19 (Varview)
                            Functional Consequence:
                            genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000016/2 (ExAC)
                            G=0.000028/7 (GnomAD_exomes)
                            HGVS:
                            14.

                            rs778659754 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>A [Show Flanks]
                              Chromosome:
                              1:206772542 (GRCh38)
                              1:206945887 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:206772541:C:A
                              Gene:
                              IL10 (Varview), IL19 (Varview)
                              Functional Consequence:
                              genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              A=0.000071/1 (ALFA)
                              A=0./0 (TWINSUK)
                              A=0.00003/8 (TOPMED)
                              A=0.000043/6 (GnomAD)
                              A=0.000259/1 (ALSPAC)
                              HGVS:
                              15.

                              rs778287916 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                1:206770221 (GRCh38)
                                1:206943566 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:206770220:C:T
                                Gene:
                                IL10 (Varview), IL19 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.000071/1 (ALFA)
                                T=0./0 (ALSPAC)
                                T=0.000042/11 (TOPMED)
                                T=0.000064/9 (GnomAD)
                                T=0.00027/1 (TWINSUK)
                                HGVS:
                                16.

                                rs778287644 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  C>- [Show Flanks]
                                  Chromosome:
                                  1:206771338 (GRCh38)
                                  1:206944683 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:206771337:CCCC:CCC
                                  Gene:
                                  IL10 (Varview), IL19 (Varview)
                                  Functional Consequence:
                                  genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
                                  Validated:
                                  by frequency,by cluster
                                  MAF:
                                  -=0.000004/1 (GnomAD_exomes)
                                  -=0.000008/1 (ExAC)
                                  HGVS:
                                  17.

                                  rs778094637 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    G>- [Show Flanks]
                                    Chromosome:
                                    1:206774454 (GRCh38)
                                    1:206947799 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:206774453:GGG:GG
                                    Gene:
                                    IL10 (Varview), IL19 (Varview)
                                    Functional Consequence:
                                    genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    GG=0.000071/1 (ALFA)
                                    -=0.000004/1 (TOPMED)
                                    -=0.000007/1 (GnomAD)
                                    HGVS:
                                    18.

                                    rs777665568 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      1:206772376 (GRCh38)
                                      1:206945721 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:206772375:T:C
                                      Gene:
                                      IL10 (Varview), IL19 (Varview)
                                      Functional Consequence:
                                      synonymous_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      C=0.000004/1 (GnomAD_exomes)
                                      C=0.000008/1 (ExAC)
                                      HGVS:
                                      19.

                                      rs777582308 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A,T [Show Flanks]
                                        Chromosome:
                                        1:206770984 (GRCh38)
                                        1:206944329 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:206770983:G:A,NC_000001.11:206770983:G:T
                                        Gene:
                                        IL10 (Varview), IL19 (Varview)
                                        Functional Consequence:
                                        intron_variant,5_prime_UTR_variant,upstream_transcript_variant,stop_gained,genic_upstream_transcript_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0.000048/1 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        A=0.000007/1 (GnomAD)
                                        T=0.000008/1 (ExAC)
                                        T=0.000008/2 (GnomAD_exomes)
                                        HGVS:
                                        20.

                                        rs777530778 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          1:206771309 (GRCh38)
                                          1:206944654 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:206771308:C:T
                                          Gene:
                                          IL10 (Varview), IL19 (Varview)
                                          Functional Consequence:
                                          genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0./0 (GnomAD)
                                          T=0.000064/16 (GnomAD_exomes)
                                          T=0.000066/8 (ExAC)
                                          HGVS:

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