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Items: 1 to 20 of 979

1.

rs1491376968 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->CGTGTGTGTG,CGTGTGTGTGTG [Show Flanks]
    Chromosome:
    22:24764625 (GRCh38)
    22:25160593 (GRCh37)
    Canonical SPDI:
    NC_000022.11:24764625:G:GCGTGTGTGTG,NC_000022.11:24764625:G:GCGTGTGTGTGTG
    Gene:
    TOP1P2 (Varview), PIWIL3 (Varview)
    Functional Consequence:
    non_coding_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    GCGTGTGTGTGTG=0./0 (ALFA)
    GCGTGTGTGTGT=0.000004/1 (TOPMED)
    GCGTGTGTGT=0.000008/1 (GnomAD)
    HGVS:

    2.

    rs1491268227 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CG>- [Show Flanks]
      Chromosome:
      22:24764625 (GRCh38)
      22:25160592 (GRCh37)
      Canonical SPDI:
      NC_000022.11:24764624:CG:
      Gene:
      TOP1P2 (Varview), PIWIL3 (Varview)
      Functional Consequence:
      non_coding_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0.00027/5 (ALFA)
      -=0.00019/11 (GnomAD)
      HGVS:

      3.

      rs1490564362 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        G>- [Show Flanks]
        Chromosome:
        22:24763163 (GRCh38)
        22:25159130 (GRCh37)
        Canonical SPDI:
        NC_000022.11:24763162:G:
        Gene:
        TOP1P2 (Varview), PIWIL3 (Varview)
        Functional Consequence:
        2KB_upstream_variant,intron_variant,upstream_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0./0 (ALFA)
        HGVS:

        4.

        rs1490069778 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>T [Show Flanks]
          Chromosome:
          22:24762513 (GRCh38)
          22:25158480 (GRCh37)
          Canonical SPDI:
          NC_000022.11:24762512:G:T
          Gene:
          TOP1P2 (Varview), PIWIL3 (Varview)
          Functional Consequence:
          2KB_upstream_variant,5_prime_UTR_variant,upstream_transcript_variant,non_coding_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (GnomAD_exomes)
          T=0.000004/1 (TOPMED)
          HGVS:

          5.

          rs1489060161 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C,G [Show Flanks]
            Chromosome:
            22:24764767 (GRCh38)
            22:25160734 (GRCh37)
            Canonical SPDI:
            NC_000022.11:24764766:T:C,NC_000022.11:24764766:T:G
            Gene:
            TOP1P2 (Varview), PIWIL3 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000014/2 (GnomAD)
            G=0.000015/4 (TOPMED)
            HGVS:

            6.

            rs1488839108 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>T [Show Flanks]
              Chromosome:
              22:24763987 (GRCh38)
              22:25159954 (GRCh37)
              Canonical SPDI:
              NC_000022.11:24763986:A:T
              Gene:
              TOP1P2 (Varview), PIWIL3 (Varview)
              Functional Consequence:
              2KB_upstream_variant,intron_variant,upstream_transcript_variant
              Validated:
              by frequency,by alfa
              MAF:
              T=0.00007/1 (ALFA)
              HGVS:

              7.

              rs1487535849 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                22:24765662 (GRCh38)
                22:25161629 (GRCh37)
                Canonical SPDI:
                NC_000022.11:24765661:G:A
                Gene:
                TOP1P2 (Varview), PIWIL3 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                A=0./0 (ALFA)
                A=0.000004/1 (TOPMED)
                HGVS:

                8.

                rs1487395260 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  G>- [Show Flanks]
                  Chromosome:
                  22:24764677 (GRCh38)
                  22:25160644 (GRCh37)
                  Canonical SPDI:
                  NC_000022.11:24764676:GG:G
                  Gene:
                  TOP1P2 (Varview), PIWIL3 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  GG=0./0 (ALFA)
                  -=0.000004/1 (TOPMED)
                  -=0.000013/1 (GnomAD)
                  HGVS:

                  9.

                  rs1486923664 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>T [Show Flanks]
                    Chromosome:
                    22:24763123 (GRCh38)
                    22:25159090 (GRCh37)
                    Canonical SPDI:
                    NC_000022.11:24763122:A:T
                    Gene:
                    TOP1P2 (Varview), PIWIL3 (Varview)
                    Functional Consequence:
                    2KB_upstream_variant,intron_variant,upstream_transcript_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000015/4 (TOPMED)
                    HGVS:

                    10.

                    rs1486736746 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      ->AGCT [Show Flanks]
                      Chromosome:
                      22:24764213 (GRCh38)
                      22:25160181 (GRCh37)
                      Canonical SPDI:
                      NC_000022.11:24764213:AGCT:AGCTAGCT
                      Gene:
                      TOP1P2 (Varview), PIWIL3 (Varview)
                      Functional Consequence:
                      2KB_upstream_variant,intron_variant,upstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      AGCTAGCT=0./0 (ALFA)
                      AGCT=0.000007/1 (GnomAD)
                      HGVS:

                      11.

                      rs1485901542 [Homo sapiens]
                        Variant type:
                        INS
                        Alleles:
                        ->G [Show Flanks]
                        Chromosome:
                        22:24766047 (GRCh38)
                        22:25162015 (GRCh37)
                        Canonical SPDI:
                        NC_000022.11:24766047::G
                        Gene:
                        TOP1P2 (Varview), PIWIL3 (Varview)
                        Functional Consequence:
                        downstream_transcript_variant,intron_variant,500B_downstream_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0./0 (ALFA)
                        G=0.000007/1 (GnomAD)
                        G=0.000011/3 (TOPMED)
                        HGVS:

                        12.

                        rs1485783298 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>T [Show Flanks]
                          Chromosome:
                          22:24764674 (GRCh38)
                          22:25160641 (GRCh37)
                          Canonical SPDI:
                          NC_000022.11:24764673:A:T
                          Gene:
                          TOP1P2 (Varview), PIWIL3 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,intron_variant
                          HGVS:

                          13.

                          rs1485771789 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            22:24765894 (GRCh38)
                            22:25161861 (GRCh37)
                            Canonical SPDI:
                            NC_000022.11:24765893:C:T
                            Gene:
                            TOP1P2 (Varview), PIWIL3 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            T=0.0025/11 (ALFA)
                            HGVS:

                            14.

                            rs1485756632 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              22:24763215 (GRCh38)
                              22:25159182 (GRCh37)
                              Canonical SPDI:
                              NC_000022.11:24763214:G:A
                              Gene:
                              TOP1P2 (Varview), PIWIL3 (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,intron_variant,upstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              A=0.000132/2 (ALFA)
                              A=0.000004/1 (TOPMED)
                              A=0.000014/2 (GnomAD)
                              A=0.000446/2 (Estonian)
                              HGVS:

                              15.

                              rs1485740171 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>A,C [Show Flanks]
                                Chromosome:
                                22:24763766 (GRCh38)
                                22:25159733 (GRCh37)
                                Canonical SPDI:
                                NC_000022.11:24763765:T:A,NC_000022.11:24763765:T:C
                                Gene:
                                TOP1P2 (Varview), PIWIL3 (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,intron_variant,upstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                C=0.03119/370 (ALFA)
                                C=0.00686/20 (KOREAN)
                                HGVS:

                                16.

                                rs1485242309 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  22:24762994 (GRCh38)
                                  22:25158961 (GRCh37)
                                  Canonical SPDI:
                                  NC_000022.11:24762993:G:A
                                  Gene:
                                  TOP1P2 (Varview), PIWIL3 (Varview)
                                  Functional Consequence:
                                  2KB_upstream_variant,intron_variant,upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1483284009 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    22:24765527 (GRCh38)
                                    22:25161494 (GRCh37)
                                    Canonical SPDI:
                                    NC_000022.11:24765526:T:C
                                    Gene:
                                    TOP1P2 (Varview), PIWIL3 (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=0.000008/2 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1483004200 has merged into rs140531011 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      GTGTGTGTGTGTGTGTGTGTGTGTGTGT>-,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
                                      Chromosome:
                                      22:24764642 (GRCh38)
                                      22:25160609 (GRCh37)
                                      Canonical SPDI:
                                      NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000022.11:24764625:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                                      Gene:
                                      TOP1P2 (Varview), PIWIL3 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      GTGTGTGTGTGTGTGT=0./0 (ALFA)
                                      -=0.2248/1126 (1000Genomes)
                                      HGVS:
                                      NC_000022.11:g.24764626GT[8], NC_000022.11:g.24764626GT[10], NC_000022.11:g.24764626GT[11], NC_000022.11:g.24764626GT[12], NC_000022.11:g.24764626GT[13], NC_000022.11:g.24764626GT[14], NC_000022.11:g.24764626GT[15], NC_000022.11:g.24764626GT[16], NC_000022.11:g.24764626GT[17], NC_000022.11:g.24764626GT[18], NC_000022.11:g.24764626GT[19], NC_000022.11:g.24764626GT[20], NC_000022.11:g.24764626GT[21], NC_000022.11:g.24764626GT[23], NC_000022.11:g.24764626GT[24], NC_000022.11:g.24764626GT[25], NC_000022.11:g.24764626GT[26], NC_000022.11:g.24764626GT[27], NC_000022.11:g.24764626GT[28], NC_000022.11:g.24764626GT[29], NC_000022.11:g.24764626GT[30], NC_000022.11:g.24764626GT[31], NC_000022.11:g.24764626GT[32], NC_000022.11:g.24764626GT[33], NC_000022.11:g.24764626GT[34], NC_000022.11:g.24764626GT[35], NC_000022.11:g.24764626GT[36], NC_000022.11:g.24764626GT[37], NC_000022.11:g.24764626GT[38], NC_000022.11:g.24764626GT[39], NC_000022.11:g.24764626GT[40], NC_000022.11:g.24764626GT[41], NC_000022.11:g.24764626GT[42], NC_000022.11:g.24764626GT[43], NC_000022.11:g.24764626GT[44], NC_000022.11:g.24764626GT[46], NC_000022.10:g.25160593GT[8], NC_000022.10:g.25160593GT[10], NC_000022.10:g.25160593GT[11], NC_000022.10:g.25160593GT[12], NC_000022.10:g.25160593GT[13], NC_000022.10:g.25160593GT[14], NC_000022.10:g.25160593GT[15], NC_000022.10:g.25160593GT[16], NC_000022.10:g.25160593GT[17], NC_000022.10:g.25160593GT[18], NC_000022.10:g.25160593GT[19], NC_000022.10:g.25160593GT[20], NC_000022.10:g.25160593GT[21], NC_000022.10:g.25160593GT[23], NC_000022.10:g.25160593GT[24], NC_000022.10:g.25160593GT[25], NC_000022.10:g.25160593GT[26], NC_000022.10:g.25160593GT[27], NC_000022.10:g.25160593GT[28], NC_000022.10:g.25160593GT[29], NC_000022.10:g.25160593GT[30], NC_000022.10:g.25160593GT[31], NC_000022.10:g.25160593GT[32], NC_000022.10:g.25160593GT[33], NC_000022.10:g.25160593GT[34], NC_000022.10:g.25160593GT[35], NC_000022.10:g.25160593GT[36], NC_000022.10:g.25160593GT[37], NC_000022.10:g.25160593GT[38], NC_000022.10:g.25160593GT[39], NC_000022.10:g.25160593GT[40], NC_000022.10:g.25160593GT[41], NC_000022.10:g.25160593GT[42], NC_000022.10:g.25160593GT[43], NC_000022.10:g.25160593GT[44], NC_000022.10:g.25160593GT[46], NR_001283.1:n.126GT[8], NR_001283.1:n.126GT[10], NR_001283.1:n.126GT[11], NR_001283.1:n.126GT[12], NR_001283.1:n.126GT[13], NR_001283.1:n.126GT[14], NR_001283.1:n.126GT[15], NR_001283.1:n.126GT[16], NR_001283.1:n.126GT[17], NR_001283.1:n.126GT[18], NR_001283.1:n.126GT[19], NR_001283.1:n.126GT[20], NR_001283.1:n.126GT[21], NR_001283.1:n.126GT[23], NR_001283.1:n.126GT[24], NR_001283.1:n.126GT[25], NR_001283.1:n.126GT[26], NR_001283.1:n.126GT[27], NR_001283.1:n.126GT[28], NR_001283.1:n.126GT[29], NR_001283.1:n.126GT[30], NR_001283.1:n.126GT[31], NR_001283.1:n.126GT[32], NR_001283.1:n.126GT[33], NR_001283.1:n.126GT[34], NR_001283.1:n.126GT[35], NR_001283.1:n.126GT[36], NR_001283.1:n.126GT[37], NR_001283.1:n.126GT[38], NR_001283.1:n.126GT[39], NR_001283.1:n.126GT[40], NR_001283.1:n.126GT[41], NR_001283.1:n.126GT[42], NR_001283.1:n.126GT[43], NR_001283.1:n.126GT[44], NR_001283.1:n.126GT[46]

                                      19.

                                      rs1481314896 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        22:24763474 (GRCh38)
                                        22:25159441 (GRCh37)
                                        Canonical SPDI:
                                        NC_000022.11:24763473:T:C
                                        Gene:
                                        TOP1P2 (Varview), PIWIL3 (Varview)
                                        Functional Consequence:
                                        2KB_upstream_variant,intron_variant,upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1481073163 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          22:24766419 (GRCh38)
                                          22:25162386 (GRCh37)
                                          Canonical SPDI:
                                          NC_000022.11:24766418:C:T
                                          Gene:
                                          TOP1P2 (Varview), PIWIL3 (Varview)
                                          Functional Consequence:
                                          downstream_transcript_variant,intron_variant,500B_downstream_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0.000004/1 (TOPMED)
                                          T=0.000014/2 (GnomAD)
                                          T=0.000035/1 (TOMMO)
                                          C=0.5/1 (SGDP_PRJ)
                                          HGVS:

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