U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 1000

1.

rs1491181056 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    TA>- [Show Flanks]
    Chromosome:
    16:24672881 (GRCh38)
    16:24684202 (GRCh37)
    Canonical SPDI:
    NC_000016.10:24672880:TA:
    Gene:
    TNRC6A (Varview), LINC01567 (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant
    Validated:
    by cluster
    HGVS:
    2.

    rs1491163654 has merged into rs1164353374 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
      Chromosome:
      16:24666652 (GRCh38)
      16:24677973 (GRCh37)
      Canonical SPDI:
      NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
      Gene:
      TNRC6A (Varview), LINC01567 (Varview)
      Functional Consequence:
      genic_upstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAAAA=0./0 (ALFA)
      HGVS:
      NC_000016.10:g.24666652_24666669del, NC_000016.10:g.24666653_24666669del, NC_000016.10:g.24666654_24666669del, NC_000016.10:g.24666655_24666669del, NC_000016.10:g.24666656_24666669del, NC_000016.10:g.24666657_24666669del, NC_000016.10:g.24666658_24666669del, NC_000016.10:g.24666659_24666669del, NC_000016.10:g.24666660_24666669del, NC_000016.10:g.24666661_24666669del, NC_000016.10:g.24666662_24666669del, NC_000016.10:g.24666663_24666669del, NC_000016.10:g.24666664_24666669del, NC_000016.10:g.24666665_24666669del, NC_000016.10:g.24666666_24666669del, NC_000016.10:g.24666667_24666669del, NC_000016.10:g.24666668_24666669del, NC_000016.10:g.24666669del, NC_000016.10:g.24666669dup, NC_000016.10:g.24666668_24666669dup, NC_000016.10:g.24666667_24666669dup, NC_000016.10:g.24666666_24666669dup, NC_000016.10:g.24666665_24666669dup, NC_000016.10:g.24666664_24666669dup, NC_000016.10:g.24666663_24666669dup, NC_000016.10:g.24666662_24666669dup, NC_000016.10:g.24666661_24666669dup, NC_000016.10:g.24666660_24666669dup, NC_000016.9:g.24677973_24677990del, NC_000016.9:g.24677974_24677990del, NC_000016.9:g.24677975_24677990del, NC_000016.9:g.24677976_24677990del, NC_000016.9:g.24677977_24677990del, NC_000016.9:g.24677978_24677990del, NC_000016.9:g.24677979_24677990del, NC_000016.9:g.24677980_24677990del, NC_000016.9:g.24677981_24677990del, NC_000016.9:g.24677982_24677990del, NC_000016.9:g.24677983_24677990del, NC_000016.9:g.24677984_24677990del, NC_000016.9:g.24677985_24677990del, NC_000016.9:g.24677986_24677990del, NC_000016.9:g.24677987_24677990del, NC_000016.9:g.24677988_24677990del, NC_000016.9:g.24677989_24677990del, NC_000016.9:g.24677990del, NC_000016.9:g.24677990dup, NC_000016.9:g.24677989_24677990dup, NC_000016.9:g.24677988_24677990dup, NC_000016.9:g.24677987_24677990dup, NC_000016.9:g.24677986_24677990dup, NC_000016.9:g.24677985_24677990dup, NC_000016.9:g.24677984_24677990dup, NC_000016.9:g.24677983_24677990dup, NC_000016.9:g.24677982_24677990dup, NC_000016.9:g.24677981_24677990dup
      3.

      rs1491062622 has merged into rs1555486918 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AA>-,AAAA,AAAAAA,AAAAAAAA [Show Flanks]
        Chromosome:
        16:24664815 (GRCh38)
        16:24676136 (GRCh37)
        Canonical SPDI:
        NC_000016.10:24664812:AAAA:AA,NC_000016.10:24664812:AAAA:AAAAAA,NC_000016.10:24664812:AAAA:AAAAAAAA,NC_000016.10:24664812:AAAA:AAAAAAAAAA
        Gene:
        TNRC6A (Varview), LINC01567 (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        AAAAAA=0./0 (ALFA)
        AAAA=0.000016/2 (GnomAD_exomes)
        -=0.000832/8 (ExAC)
        HGVS:
        4.

        rs1491017566 has merged into rs61045296 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AA>-,A,AAA [Show Flanks]
          Chromosome:
          16:24669499 (GRCh38)
          16:24680820 (GRCh37)
          Canonical SPDI:
          NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAAAAA
          Gene:
          TNRC6A (Varview), LINC01567 (Varview)
          Functional Consequence:
          intron_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          AAAAAAAAAAAAAA=0./0 (ALFA)
          A=0.282149/1413 (1000Genomes)
          A=0.340145/90033 (TOPMED)
          A=0.426667/256 (NorthernSweden)
          A=0.474831/1830 (ALSPAC)
          A=0.488943/1813 (TWINSUK)
          A=0.5/20 (GENOME_DK)
          HGVS:
          5.

          rs1490852084 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            16:24661414 (GRCh38)
            16:24672735 (GRCh37)
            Canonical SPDI:
            NC_000016.10:24661413:T:C
            Gene:
            TNRC6A (Varview), LINC01567 (Varview)
            Functional Consequence:
            downstream_transcript_variant,500B_downstream_variant,intron_variant,genic_upstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0./0 (ALFA)
            C=0.000004/1 (TOPMED)
            C=0.000007/1 (GnomAD)
            HGVS:
            6.

            rs1490830628 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>T [Show Flanks]
              Chromosome:
              16:24664742 (GRCh38)
              16:24676063 (GRCh37)
              Canonical SPDI:
              NC_000016.10:24664741:A:T
              Gene:
              TNRC6A (Varview), LINC01567 (Varview)
              Functional Consequence:
              intron_variant,genic_upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0.000671/3 (ALFA)
              T=0.000022/3 (GnomAD)
              T=0.00067/3 (Estonian)
              HGVS:
              7.

              rs1490755409 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A [Show Flanks]
                Chromosome:
                16:24667627 (GRCh38)
                16:24678948 (GRCh37)
                Canonical SPDI:
                NC_000016.10:24667626:T:A
                Gene:
                TNRC6A (Varview), LINC01567 (Varview)
                Functional Consequence:
                intron_variant,genic_upstream_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                A=0./0 (ALFA)
                HGVS:
                8.

                rs1490362403 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A,C [Show Flanks]
                  Chromosome:
                  16:24661828 (GRCh38)
                  16:24673149 (GRCh37)
                  Canonical SPDI:
                  NC_000016.10:24661827:G:A,NC_000016.10:24661827:G:C
                  Gene:
                  TNRC6A (Varview), LINC01567 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000007/1 (GnomAD)
                  HGVS:
                  9.

                  rs1490266693 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    16:24668059 (GRCh38)
                    16:24679380 (GRCh37)
                    Canonical SPDI:
                    NC_000016.10:24668058:G:A
                    Gene:
                    TNRC6A (Varview), LINC01567 (Varview)
                    Functional Consequence:
                    intron_variant,genic_upstream_transcript_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    A=0./0 (ALFA)
                    HGVS:
                    10.

                    rs1489872236 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      16:24662279 (GRCh38)
                      16:24673600 (GRCh37)
                      Canonical SPDI:
                      NC_000016.10:24662278:G:A
                      Gene:
                      TNRC6A (Varview), LINC01567 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000008/2 (TOPMED)
                      A=0.000016/2 (GnomAD)
                      HGVS:
                      11.

                      rs1489827293 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A,T [Show Flanks]
                        Chromosome:
                        16:24669479 (GRCh38)
                        16:24680800 (GRCh37)
                        Canonical SPDI:
                        NC_000016.10:24669478:C:A,NC_000016.10:24669478:C:T
                        Gene:
                        TNRC6A (Varview), LINC01567 (Varview)
                        Functional Consequence:
                        intron_variant,genic_upstream_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        HGVS:
                        12.

                        rs1489641087 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          16:24663271 (GRCh38)
                          16:24674592 (GRCh37)
                          Canonical SPDI:
                          NC_000016.10:24663270:G:A
                          Gene:
                          TNRC6A (Varview), LINC01567 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          A=0.000071/1 (ALFA)
                          A=0.000004/1 (TOPMED)
                          HGVS:
                          13.

                          rs1489573668 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>C [Show Flanks]
                            Chromosome:
                            16:24661955 (GRCh38)
                            16:24673276 (GRCh37)
                            Canonical SPDI:
                            NC_000016.10:24661954:G:C
                            Gene:
                            TNRC6A (Varview), LINC01567 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000004/1 (TOPMED)
                            C=0.000007/1 (GnomAD)
                            HGVS:
                            14.

                            rs1489187759 [Homo sapiens]
                              Variant type:
                              DEL
                              Alleles:
                              A>- [Show Flanks]
                              Chromosome:
                              16:24665990 (GRCh38)
                              16:24677311 (GRCh37)
                              Canonical SPDI:
                              NC_000016.10:24665989:A:
                              Gene:
                              TNRC6A (Varview), LINC01567 (Varview)
                              Functional Consequence:
                              intron_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              -=0./0 (ALFA)
                              -=0.000004/1 (TOPMED)
                              -=0.000014/2 (GnomAD)
                              HGVS:
                              15.

                              rs1489158576 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                16:24664971 (GRCh38)
                                16:24676292 (GRCh37)
                                Canonical SPDI:
                                NC_000016.10:24664970:G:A
                                Gene:
                                TNRC6A (Varview), LINC01567 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                A=0.000111/1 (ALFA)
                                A=0.000007/1 (GnomAD_exomes)
                                HGVS:
                                16.

                                rs1488933830 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>C,G [Show Flanks]
                                  Chromosome:
                                  16:24670722 (GRCh38)
                                  16:24682043 (GRCh37)
                                  Canonical SPDI:
                                  NC_000016.10:24670721:A:C,NC_000016.10:24670721:A:G
                                  Gene:
                                  TNRC6A (Varview), LINC01567 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000004/1 (TOPMED)
                                  C=0.001638/3 (Korea1K)
                                  HGVS:
                                  17.

                                  rs1488026554 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>A [Show Flanks]
                                    Chromosome:
                                    16:24664319 (GRCh38)
                                    16:24675640 (GRCh37)
                                    Canonical SPDI:
                                    NC_000016.10:24664318:T:A
                                    Gene:
                                    TNRC6A (Varview), LINC01567 (Varview)
                                    Functional Consequence:
                                    intron_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    A=0.000071/1 (ALFA)
                                    A=0.000015/4 (TOPMED)
                                    HGVS:
                                    18.

                                    rs1487880842 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>G [Show Flanks]
                                      Chromosome:
                                      16:24670127 (GRCh38)
                                      16:24681448 (GRCh37)
                                      Canonical SPDI:
                                      NC_000016.10:24670126:T:G
                                      Gene:
                                      TNRC6A (Varview), LINC01567 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000019/5 (TOPMED)
                                      G=0.000021/3 (GnomAD)
                                      HGVS:
                                      19.

                                      rs1487290340 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        16:24667463 (GRCh38)
                                        16:24678784 (GRCh37)
                                        Canonical SPDI:
                                        NC_000016.10:24667462:A:G
                                        Gene:
                                        TNRC6A (Varview), LINC01567 (Varview)
                                        Functional Consequence:
                                        genic_upstream_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        G=0.000071/1 (ALFA)
                                        G=0.000007/1 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1486871952 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          16:24671215 (GRCh38)
                                          16:24682536 (GRCh37)
                                          Canonical SPDI:
                                          NC_000016.10:24671214:A:G
                                          Gene:
                                          TNRC6A (Varview), LINC01567 (Varview)
                                          Functional Consequence:
                                          upstream_transcript_variant,genic_upstream_transcript_variant,intron_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:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...