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Items: 1 to 20 of 7366

1.

rs1491502953 has merged into rs549012700 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    GCGC>-,GC,GCGCGC,GCGCGCGC,GCGCGCGCGC,GCGCGCGCGCGC,GCGCGCGCGCGCGC,GCGCGCGCGCGCGCGC [Show Flanks]
    Chromosome:
    17:35266184 (GRCh38)
    17:33593203 (GRCh37)
    Canonical SPDI:
    NC_000017.11:35266177:GCGCGCGCGC:GCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC,NC_000017.11:35266177:GCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC
    Gene:
    SLFN5 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    GCGCGCGC=0./0 (ALFA)
    -=0.17063/2859 (TOMMO)
    -=0.18668/342 (Korea1K)
    HGVS:
    NC_000017.11:g.35266178GC[3], NC_000017.11:g.35266178GC[4], NC_000017.11:g.35266178GC[6], NC_000017.11:g.35266178GC[7], NC_000017.11:g.35266178GC[8], NC_000017.11:g.35266178GC[9], NC_000017.11:g.35266178GC[10], NC_000017.11:g.35266178GC[11], NC_000017.10:g.33593197GC[3], NC_000017.10:g.33593197GC[4], NC_000017.10:g.33593197GC[6], NC_000017.10:g.33593197GC[7], NC_000017.10:g.33593197GC[8], NC_000017.10:g.33593197GC[9], NC_000017.10:g.33593197GC[10], NC_000017.10:g.33593197GC[11], NM_144975.4:c.*290GC[3], NM_144975.4:c.*290GC[4], NM_144975.4:c.*290GC[6], NM_144975.4:c.*290GC[7], NM_144975.4:c.*290GC[8], NM_144975.4:c.*290GC[9], NM_144975.4:c.*290GC[10], NM_144975.4:c.*290GC[11], NM_144975.3:c.*290GC[3], NM_144975.3:c.*290GC[4], NM_144975.3:c.*290GC[6], NM_144975.3:c.*290GC[7], NM_144975.3:c.*290GC[8], NM_144975.3:c.*290GC[9], NM_144975.3:c.*290GC[10], NM_144975.3:c.*290GC[11], NM_001330183.2:c.*1075GC[3], NM_001330183.2:c.*1075GC[4], NM_001330183.2:c.*1075GC[6], NM_001330183.2:c.*1075GC[7], NM_001330183.2:c.*1075GC[8], NM_001330183.2:c.*1075GC[9], NM_001330183.2:c.*1075GC[10], NM_001330183.2:c.*1075GC[11], NM_001330183.1:c.*1075GC[3], NM_001330183.1:c.*1075GC[4], NM_001330183.1:c.*1075GC[6], NM_001330183.1:c.*1075GC[7], NM_001330183.1:c.*1075GC[8], NM_001330183.1:c.*1075GC[9], NM_001330183.1:c.*1075GC[10], NM_001330183.1:c.*1075GC[11]

    2.

    rs1491343226 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      GA>- [Show Flanks]
      Chromosome:
      17:35263827 (GRCh38)
      17:33590846 (GRCh37)
      Canonical SPDI:
      NC_000017.11:35263825:AGA:A
      Gene:
      SLFN5 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0.00008/1 (ALFA)
      HGVS:

      3.

      rs1491193664 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        AT>- [Show Flanks]
        Chromosome:
        17:35266142 (GRCh38)
        17:33593161 (GRCh37)
        Canonical SPDI:
        NC_000017.11:35266141:AT:
        Gene:
        SLFN5 (Varview)
        Functional Consequence:
        3_prime_UTR_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0.001517/18 (ALFA)
        -=0.001762/184 (GnomAD)
        HGVS:

        4.

        rs1491071602 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->TG [Show Flanks]
          Chromosome:
          17:35253714 (GRCh38)
          17:33580734 (GRCh37)
          Canonical SPDI:
          NC_000017.11:35253714:TG:TGTG
          Gene:
          SLFN5 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          TGTG=0./0 (ALFA)
          TG=0.000004/1 (TOPMED)
          HGVS:

          5.

          rs1491064619 has merged into rs200709274 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
            Chromosome:
            17:35261688 (GRCh38)
            17:33588707 (GRCh37)
            Canonical SPDI:
            NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:35261675:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
            Gene:
            SLFN5 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TTTTTTTTTTTTT=0./0 (ALFA)
            -=0.2813/1409 (1000Genomes)
            HGVS:

            6.

            rs1491033614 has merged into rs35223656 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              AA>-,A,AAA,AAAA [Show Flanks]
              Chromosome:
              17:35246869 (GRCh38)
              17:33573888 (GRCh37)
              Canonical SPDI:
              NC_000017.11:35246855:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:35246855:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:35246855:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:35246855:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA
              Gene:
              SLFN5 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              AAAAAAAAAAAAAAAAA=0.00016/2 (ALFA)
              A=0.09322/55 (NorthernSweden)
              A=0.15/6 (GENOME_DK)
              HGVS:

              7.

              rs1490902751 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C,G [Show Flanks]
                Chromosome:
                17:35258596 (GRCh38)
                17:33585615 (GRCh37)
                Canonical SPDI:
                NC_000017.11:35258595:T:C,NC_000017.11:35258595:T:G
                Gene:
                SLFN5 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                G=0./0 (ALFA)
                G=0.000008/2 (TOPMED)
                HGVS:

                8.

                rs1490900936 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  17:35273034 (GRCh38)
                  17:33600053 (GRCh37)
                  Canonical SPDI:
                  NC_000017.11:35273033:A:G
                  Gene:
                  SLFN5 (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  HGVS:

                  9.

                  rs1490847751 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C,G [Show Flanks]
                    Chromosome:
                    17:35257430 (GRCh38)
                    17:33584449 (GRCh37)
                    Canonical SPDI:
                    NC_000017.11:35257429:T:C,NC_000017.11:35257429:T:G
                    Gene:
                    SLFN5 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000014/2 (GnomAD)
                    C=0.000015/4 (TOPMED)
                    G=0.001638/3 (Korea1K)
                    HGVS:

                    10.

                    rs1490833608 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      17:35241311 (GRCh38)
                      17:33568330 (GRCh37)
                      Canonical SPDI:
                      NC_000017.11:35241310:G:A
                      Gene:
                      SLFN5 (Varview), LOC105371932 (Varview)
                      Functional Consequence:
                      2KB_upstream_variant,upstream_transcript_variant,3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000011/3 (TOPMED)
                      G=0.5/6 (SGDP_PRJ)
                      HGVS:

                      11.

                      rs1490817964 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        17:35242487 (GRCh38)
                        17:33569506 (GRCh37)
                        Canonical SPDI:
                        NC_000017.11:35242486:T:C
                        Gene:
                        SLFN5 (Varview), LOC105371932 (Varview)
                        Functional Consequence:
                        2KB_upstream_variant,upstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000004/1 (TOPMED)
                        C=0.000014/2 (GnomAD)
                        HGVS:

                        12.

                        rs1490562615 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>T [Show Flanks]
                          Chromosome:
                          17:35249626 (GRCh38)
                          17:33576645 (GRCh37)
                          Canonical SPDI:
                          NC_000017.11:35249625:A:T
                          Gene:
                          SLFN5 (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)
                          HGVS:

                          13.

                          rs1490415731 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G [Show Flanks]
                            Chromosome:
                            17:35258063 (GRCh38)
                            17:33585082 (GRCh37)
                            Canonical SPDI:
                            NC_000017.11:35258062:C:G
                            Gene:
                            SLFN5 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000011/3 (TOPMED)
                            HGVS:

                            14.

                            rs1490371719 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              17:35242010 (GRCh38)
                              17:33569029 (GRCh37)
                              Canonical SPDI:
                              NC_000017.11:35242009:C:T
                              Gene:
                              SLFN5 (Varview), LOC105371932 (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,upstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000007/1 (GnomAD)
                              T=0.000008/2 (TOPMED)
                              HGVS:

                              15.

                              rs1490344503 has merged into rs58644233 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TGTGTGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
                                Chromosome:
                                17:35266161 (GRCh38)
                                17:33593180 (GRCh37)
                                Canonical SPDI:
                                NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:35266142:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
                                Gene:
                                SLFN5 (Varview)
                                Functional Consequence:
                                3_prime_UTR_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TGTGTGTGTGTGTGTGTGTG=0./0 (ALFA)
                                -=0.000019/5 (TOPMED)
                                HGVS:
                                NC_000017.11:g.35266143TG[9], NC_000017.11:g.35266143TG[10], NC_000017.11:g.35266143TG[11], NC_000017.11:g.35266143TG[12], NC_000017.11:g.35266143TG[13], NC_000017.11:g.35266143TG[14], NC_000017.11:g.35266143TG[15], NC_000017.11:g.35266143TG[16], NC_000017.11:g.35266143TG[17], NC_000017.11:g.35266143TG[19], NC_000017.11:g.35266143TG[20], NC_000017.11:g.35266143TG[21], NC_000017.11:g.35266143TG[22], NC_000017.11:g.35266143TG[23], NC_000017.11:g.35266143TG[24], NC_000017.11:g.35266143TG[25], NC_000017.11:g.35266143TG[26], NC_000017.11:g.35266143TG[27], NC_000017.11:g.35266143TG[28], NC_000017.10:g.33593162TG[9], NC_000017.10:g.33593162TG[10], NC_000017.10:g.33593162TG[11], NC_000017.10:g.33593162TG[12], NC_000017.10:g.33593162TG[13], NC_000017.10:g.33593162TG[14], NC_000017.10:g.33593162TG[15], NC_000017.10:g.33593162TG[16], NC_000017.10:g.33593162TG[17], NC_000017.10:g.33593162TG[19], NC_000017.10:g.33593162TG[20], NC_000017.10:g.33593162TG[21], NC_000017.10:g.33593162TG[22], NC_000017.10:g.33593162TG[23], NC_000017.10:g.33593162TG[24], NC_000017.10:g.33593162TG[25], NC_000017.10:g.33593162TG[26], NC_000017.10:g.33593162TG[27], NC_000017.10:g.33593162TG[28], NM_144975.4:c.*255TG[9], NM_144975.4:c.*255TG[10], NM_144975.4:c.*255TG[11], NM_144975.4:c.*255TG[12], NM_144975.4:c.*255TG[13], NM_144975.4:c.*255TG[14], NM_144975.4:c.*255TG[15], NM_144975.4:c.*255TG[16], NM_144975.4:c.*255TG[17], NM_144975.4:c.*255TG[19], NM_144975.4:c.*255TG[20], NM_144975.4:c.*255TG[21], NM_144975.4:c.*255TG[22], NM_144975.4:c.*255TG[23], NM_144975.4:c.*255TG[24], NM_144975.4:c.*255TG[25], NM_144975.4:c.*255TG[26], NM_144975.4:c.*255TG[27], NM_144975.4:c.*255TG[28], NM_144975.3:c.*255TG[9], NM_144975.3:c.*255TG[10], NM_144975.3:c.*255TG[11], NM_144975.3:c.*255TG[12], NM_144975.3:c.*255TG[13], NM_144975.3:c.*255TG[14], NM_144975.3:c.*255TG[15], NM_144975.3:c.*255TG[16], NM_144975.3:c.*255TG[17], NM_144975.3:c.*255TG[19], NM_144975.3:c.*255TG[20], NM_144975.3:c.*255TG[21], NM_144975.3:c.*255TG[22], NM_144975.3:c.*255TG[23], NM_144975.3:c.*255TG[24], NM_144975.3:c.*255TG[25], NM_144975.3:c.*255TG[26], NM_144975.3:c.*255TG[27], NM_144975.3:c.*255TG[28], NM_001330183.2:c.*1040TG[9], NM_001330183.2:c.*1040TG[10], NM_001330183.2:c.*1040TG[11], NM_001330183.2:c.*1040TG[12], NM_001330183.2:c.*1040TG[13], NM_001330183.2:c.*1040TG[14], NM_001330183.2:c.*1040TG[15], NM_001330183.2:c.*1040TG[16], NM_001330183.2:c.*1040TG[17], NM_001330183.2:c.*1040TG[19], NM_001330183.2:c.*1040TG[20], NM_001330183.2:c.*1040TG[21], NM_001330183.2:c.*1040TG[22], NM_001330183.2:c.*1040TG[23], NM_001330183.2:c.*1040TG[24], NM_001330183.2:c.*1040TG[25], NM_001330183.2:c.*1040TG[26], NM_001330183.2:c.*1040TG[27], NM_001330183.2:c.*1040TG[28], NM_001330183.1:c.*1040TG[9], NM_001330183.1:c.*1040TG[10], NM_001330183.1:c.*1040TG[11], NM_001330183.1:c.*1040TG[12], NM_001330183.1:c.*1040TG[13], NM_001330183.1:c.*1040TG[14], NM_001330183.1:c.*1040TG[15], NM_001330183.1:c.*1040TG[16], NM_001330183.1:c.*1040TG[17], NM_001330183.1:c.*1040TG[19], NM_001330183.1:c.*1040TG[20], NM_001330183.1:c.*1040TG[21], NM_001330183.1:c.*1040TG[22], NM_001330183.1:c.*1040TG[23], NM_001330183.1:c.*1040TG[24], NM_001330183.1:c.*1040TG[25], NM_001330183.1:c.*1040TG[26], NM_001330183.1:c.*1040TG[27], NM_001330183.1:c.*1040TG[28]

                                16.

                                rs1490279592 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>T [Show Flanks]
                                  Chromosome:
                                  17:35251409 (GRCh38)
                                  17:33578428 (GRCh37)
                                  Canonical SPDI:
                                  NC_000017.11:35251408:G:T
                                  Gene:
                                  SLFN5 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  T=0./0 (ALFA)
                                  HGVS:

                                  17.

                                  rs1490244062 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>A [Show Flanks]
                                    Chromosome:
                                    17:35255380 (GRCh38)
                                    17:33582399 (GRCh37)
                                    Canonical SPDI:
                                    NC_000017.11:35255379:T:A
                                    Gene:
                                    SLFN5 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0.000071/1 (ALFA)
                                    A=0.000004/1 (TOPMED)
                                    A=0.000007/1 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1490209032 [Homo sapiens]
                                      Variant type:
                                      DEL
                                      Alleles:
                                      C>- [Show Flanks]
                                      Chromosome:
                                      17:35253004 (GRCh38)
                                      17:33580023 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:35253003:C:
                                      Gene:
                                      SLFN5 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      -=0./0 (ALFA)
                                      -=0.000019/5 (TOPMED)
                                      -=0.000029/4 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490129992 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        17:35273384 (GRCh38)
                                        17:33600403 (GRCh37)
                                        Canonical SPDI:
                                        NC_000017.11:35273383:A:G
                                        Gene:
                                        SLFN5 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1490115443 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>T [Show Flanks]
                                          Chromosome:
                                          17:35258924 (GRCh38)
                                          17:33585943 (GRCh37)
                                          Canonical SPDI:
                                          NC_000017.11:35258923:G:T
                                          Gene:
                                          SLFN5 (Varview)
                                          Functional Consequence:
                                          synonymous_variant,coding_sequence_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          T=0.000004/1 (GnomAD_exomes)
                                          HGVS:

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