U.S. flag

An official website of the United States government

Links from Gene

Items: 1 to 20 of 2666

1.

rs1491502868 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    AC>- [Show Flanks]
    Chromosome:
    15:58069279 (GRCh38)
    15:58361477 (GRCh37)
    Canonical SPDI:
    NC_000015.10:58069278:AC:
    Gene:
    ALDH1A2-AS1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0./0 (ALFA)
    -=0.00007/1 (TOMMO)
    -=0.00055/1 (Korea1K)
    ...more
    HGVS:
    2.

    rs1491453299 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->C [Show Flanks]
      Chromosome:
      15:58069279 (GRCh38)
      15:58361478 (GRCh37)
      Canonical SPDI:
      NC_000015.10:58069279:CC:CCC
      Gene:
      ALDH1A2-AS1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      CCC=0./0 (ALFA)
      C=0.000007/1 (GnomAD)
      HGVS:
      3.

      rs1490622183 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>T [Show Flanks]
        Chromosome:
        15:58072360 (GRCh38)
        15:58364558 (GRCh37)
        Canonical SPDI:
        NC_000015.10:58072359:A:T
        Gene:
        ALDH1A2-AS1 (Varview)
        Functional Consequence:
        non_coding_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000007/1 (GnomAD)
        HGVS:
        4.

        rs1490494989 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G [Show Flanks]
          Chromosome:
          15:58068976 (GRCh38)
          15:58361174 (GRCh37)
          Canonical SPDI:
          NC_000015.10:58068975:A:G
          Gene:
          ALDH1A2-AS1 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0./0 (ALFA)
          G=0.000004/1 (TOPMED)
          G=0.000014/2 (GnomAD)
          ...more
          HGVS:
          5.

          rs1490031149 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>G [Show Flanks]
            Chromosome:
            15:58068482 (GRCh38)
            15:58360680 (GRCh37)
            Canonical SPDI:
            NC_000015.10:58068481:C:G
            Gene:
            ALDH1A2-AS1 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            G=0.000007/1 (GnomAD)
            ...more
            HGVS:
            6.

            rs1490006756 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              15:58069392 (GRCh38)
              15:58361590 (GRCh37)
              Canonical SPDI:
              NC_000015.10:58069391:C:T
              Gene:
              ALDH1A2-AS1 (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)
              ...more
              HGVS:
              7.

              rs1489827432 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>C,T [Show Flanks]
                Chromosome:
                15:58063249 (GRCh38)
                15:58355447 (GRCh37)
                Canonical SPDI:
                NC_000015.10:58063248:G:C,NC_000015.10:58063248:G:T
                Gene:
                ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                Functional Consequence:
                2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                T=0.000014/2 (GnomAD)
                HGVS:
                8.

                rs1489785350 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A,C [Show Flanks]
                  Chromosome:
                  15:58064002 (GRCh38)
                  15:58356200 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:58064001:G:A,NC_000015.10:58064001:G:C
                  Gene:
                  ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000004/1 (TOPMED)
                  A=0.00006/1 (TOMMO)
                  ...more
                  HGVS:
                  9.

                  rs1489758207 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    15:58068580 (GRCh38)
                    15:58360778 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:58068579:C:T
                    Gene:
                    ALDH1A2-AS1 (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)
                    ...more
                    HGVS:
                    10.

                    rs1489747575 has merged into rs1240790045 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      C>-,CC [Show Flanks]
                      Chromosome:
                      15:58069505 (GRCh38)
                      15:58361703 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:58069504:CCCCCC:CCCCC,NC_000015.10:58069504:CCCCCC:CCCCCCC
                      Gene:
                      ALDH1A2-AS1 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      CCCCCCC=0./0 (ALFA)
                      -=0.000007/1 (GnomAD)
                      HGVS:
                      11.

                      rs1489047660 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        15:58065620 (GRCh38)
                        15:58357818 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:58065619:C:T
                        Gene:
                        ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                        Functional Consequence:
                        5_prime_UTR_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
                        HGVS:
                        12.

                        rs1488951271 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>A [Show Flanks]
                          Chromosome:
                          15:58066968 (GRCh38)
                          15:58359166 (GRCh37)
                          Canonical SPDI:
                          NC_000015.10:58066967:C:A
                          Gene:
                          ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000004/1 (TOPMED)
                          A=0.000014/2 (GnomAD)
                          ...more
                          HGVS:
                          13.

                          rs1488251704 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            15:58064430 (GRCh38)
                            15:58356628 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:58064429:C:A
                            Gene:
                            ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                            Functional Consequence:
                            2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            A=0./0 (ALFA)
                            A=0./0 (KOREAN)
                            A=0.000011/3 (TOPMED)
                            A=0.000177/3 (TOMMO)
                            ...more
                            HGVS:
                            14.

                            rs1488214827 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>G [Show Flanks]
                              Chromosome:
                              15:58069104 (GRCh38)
                              15:58361302 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:58069103:C:G
                              Gene:
                              ALDH1A2-AS1 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000014/2 (GnomAD)
                              G=0.000015/4 (TOPMED)
                              ...more
                              HGVS:
                              15.

                              rs1487788534 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                15:58070525 (GRCh38)
                                15:58362723 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:58070524:C:T
                                Gene:
                                ALDH1A2-AS1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000008/2 (TOPMED)
                                HGVS:
                                16.

                                rs1487135889 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  15:58066955 (GRCh38)
                                  15:58359153 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:58066954:C:T
                                  Gene:
                                  ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                                  Functional Consequence:
                                  2KB_upstream_variant,upstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0.000071/1 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  T=0.000011/3 (TOPMED)
                                  ...more
                                  HGVS:
                                  17.

                                  rs1486996068 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    15:58067832 (GRCh38)
                                    15:58360030 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:58067831:C:T
                                    Gene:
                                    ALDH1A2-AS1 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    HGVS:
                                    18.

                                    rs1486848297 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      15:58064930 (GRCh38)
                                      15:58357128 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:58064929:C:G
                                      Gene:
                                      ALDH1A2 (Varview), ALDH1A2-AS1 (Varview)
                                      Functional Consequence:
                                      2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      HGVS:
                                      19.

                                      rs1486545238 [Homo sapiens]
                                        Variant type:
                                        SNV:
                                        Alleles:
                                        CCTTT>-
                                        Chromosome:
                                        no mapping
                                        Canonical SPDI:
                                        20.

                                        rs1486519005 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>C [Show Flanks]
                                          Chromosome:
                                          15:58067899 (GRCh38)
                                          15:58360097 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:58067898:G:C
                                          Gene:
                                          ALDH1A2-AS1 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          HGVS:

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...
                                          External link. Please review our privacy policy.