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1.

rs1491558973 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    AC>- [Show Flanks]
    Chromosome:
    3:53816131 (GRCh38)
    3:53850158 (GRCh37)
    Canonical SPDI:
    NC_000003.12:53816130:AC:
    Gene:
    CHDH (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0./0 (ALFA)
    -=0.00051/7 (TOMMO)
    HGVS:
    2.

    rs1491506832 [Homo sapiens]
      Variant type:
      INS
      Alleles:
      ->A,AA [Show Flanks]
      Chromosome:
      3:53813130 (GRCh38)
      3:53847158 (GRCh37)
      Canonical SPDI:
      NC_000003.12:53813130::A,NC_000003.12:53813130::AA
      Gene:
      CACNA1D (Varview), CHDH (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AA=0./0 (ALFA)
      HGVS:
      NC_000003.12:g.53813130_53813131insA, NC_000003.12:g.53813130_53813131insAA, NC_000003.11:g.53847157_53847158insA, NC_000003.11:g.53847157_53847158insAA, NG_032999.1:g.323082_323083insA, NG_032999.1:g.323082_323083insAA, NM_000720.4:c.*1724_*1725insA, NM_000720.4:c.*1724_*1725insAA, NM_001128840.3:c.*1724_*1725insA, NM_001128840.3:c.*1724_*1725insAA, NM_001128839.3:c.*1724_*1725insA, NM_001128839.3:c.*1724_*1725insAA, NM_018397.5:c.*4646_*4647insT, NM_018397.5:c.*4646_*4647insTT, XM_005265448.4:c.*1724_*1725insA, XM_005265448.4:c.*1724_*1725insAA, XM_005265448.2:c.*1724_*1725insA, XM_005265448.2:c.*1724_*1725insAA, XM_005265448.1:c.*1724_*1725insA, XM_005265448.1:c.*1724_*1725insAA, XM_011534097.3:c.*1724_*1725insA, XM_011534097.3:c.*1724_*1725insAA, XM_011534097.2:c.*1724_*1725insA, XM_011534097.2:c.*1724_*1725insAA, XM_011534097.1:c.*1724_*1725insA, XM_011534097.1:c.*1724_*1725insAA, XM_011534094.3:c.*1724_*1725insA, XM_011534094.3:c.*1724_*1725insAA, XM_011534094.2:c.*1724_*1725insA, XM_011534094.2:c.*1724_*1725insAA, XM_011534094.1:c.*1724_*1725insA, XM_011534094.1:c.*1724_*1725insAA, XM_011534100.3:c.*1724_*1725insA, XM_011534100.3:c.*1724_*1725insAA, XM_011534100.2:c.*1724_*1725insA, XM_011534100.2:c.*1724_*1725insAA, XM_011534100.1:c.*1724_*1725insA, XM_011534100.1:c.*1724_*1725insAA, XM_011534096.3:c.*1724_*1725insA, XM_011534096.3:c.*1724_*1725insAA, XM_011534096.1:c.*1724_*1725insA, XM_011534096.1:c.*1724_*1725insAA, XM_011534099.3:c.*1724_*1725insA, XM_011534099.3:c.*1724_*1725insAA, XM_011534099.2:c.*1724_*1725insA, XM_011534099.2:c.*1724_*1725insAA, XM_011534099.1:c.*1724_*1725insA, XM_011534099.1:c.*1724_*1725insAA, XM_017007137.2:c.*1724_*1725insA, XM_017007137.2:c.*1724_*1725insAA, XM_017007137.1:c.*1724_*1725insA, XM_017007137.1:c.*1724_*1725insAA, XM_017007138.2:c.*1724_*1725insA, XM_017007138.2:c.*1724_*1725insAA, XM_017007138.1:c.*1724_*1725insA, XM_017007138.1:c.*1724_*1725insAA, XM_017007139.2:c.*1724_*1725insA, XM_017007139.2:c.*1724_*1725insAA, XM_017007139.1:c.*1724_*1725insA, XM_017007139.1:c.*1724_*1725insAA, XM_017007141.2:c.*1724_*1725insA, XM_017007141.2:c.*1724_*1725insAA, XM_017007141.1:c.*1724_*1725insA, XM_017007141.1:c.*1724_*1725insAA, XM_017007140.2:c.*1724_*1725insA, XM_017007140.2:c.*1724_*1725insAA, XM_017007140.1:c.*1724_*1725insA, XM_017007140.1:c.*1724_*1725insAA, XM_017007144.2:c.*1724_*1725insA, XM_017007144.2:c.*1724_*1725insAA, XM_017007143.2:c.*1724_*1725insA, XM_017007143.2:c.*1724_*1725insAA, XM_017007143.1:c.*1724_*1725insA, XM_017007143.1:c.*1724_*1725insAA, XM_017007142.2:c.*1724_*1725insA, XM_017007142.2:c.*1724_*1725insAA, XM_017007142.1:c.*1724_*1725insA, XM_017007142.1:c.*1724_*1725insAA, XM_017007145.2:c.*1724_*1725insA, XM_017007145.2:c.*1724_*1725insAA, XM_017007145.1:c.*1724_*1725insA, XM_017007145.1:c.*1724_*1725insAA, XM_047448871.1:c.*1724_*1725insA, XM_047448871.1:c.*1724_*1725insAA, XM_047448872.1:c.*1724_*1725insA, XM_047448872.1:c.*1724_*1725insAA
      3.

      rs1491469651 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ->AT [Show Flanks]
        Chromosome:
        3:53829887 (GRCh38)
        3:53863915 (GRCh37)
        Canonical SPDI:
        NC_000003.12:53829887:T:TAT
        Gene:
        CHDH (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        TAT=0./0 (ALFA)
        TA=0.000004/1 (TOPMED)
        HGVS:
        4.

        rs1491396647 has merged into rs1174010295 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          CCC>-,C,CC,CCCC,CCCCC [Show Flanks]
          Chromosome:
          3:53843183 (GRCh38)
          3:53877210 (GRCh37)
          Canonical SPDI:
          NC_000003.12:53843177:CCCCCCCC:CCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCCCCC
          Gene:
          CHDH (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          CCCCCCC=0./0 (ALFA)
          C=0.00047/2 (Estonian)
          HGVS:
          5.

          rs1491366160 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            TC>- [Show Flanks]
            Chromosome:
            3:53843177 (GRCh38)
            3:53877204 (GRCh37)
            Canonical SPDI:
            NC_000003.12:53843176:TC:
            Gene:
            CHDH (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            -=0.00017/2 (ALFA)
            HGVS:
            6.

            rs1491275452 has merged into rs59630779 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              3:53813142 (GRCh38)
              3:53847169 (GRCh37)
              Canonical SPDI:
              NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              CACNA1D (Varview), CHDH (Varview)
              Functional Consequence:
              genic_downstream_transcript_variant,3_prime_UTR_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTTTTTTTT=0./0 (ALFA)
              TTT=0.13/651 (1000Genomes)
              HGVS:
              NC_000003.12:g.53813142_53813152del, NC_000003.12:g.53813143_53813152del, NC_000003.12:g.53813144_53813152del, NC_000003.12:g.53813145_53813152del, NC_000003.12:g.53813146_53813152del, NC_000003.12:g.53813147_53813152del, NC_000003.12:g.53813148_53813152del, NC_000003.12:g.53813149_53813152del, NC_000003.12:g.53813150_53813152del, NC_000003.12:g.53813151_53813152del, NC_000003.12:g.53813152del, NC_000003.12:g.53813152dup, NC_000003.12:g.53813151_53813152dup, NC_000003.12:g.53813150_53813152dup, NC_000003.12:g.53813148_53813152dup, NC_000003.12:g.53813130_53813152T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.53813152_53813153insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.53813152_53813153insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.53847169_53847179del, NC_000003.11:g.53847170_53847179del, NC_000003.11:g.53847171_53847179del, NC_000003.11:g.53847172_53847179del, NC_000003.11:g.53847173_53847179del, NC_000003.11:g.53847174_53847179del, NC_000003.11:g.53847175_53847179del, NC_000003.11:g.53847176_53847179del, NC_000003.11:g.53847177_53847179del, NC_000003.11:g.53847178_53847179del, NC_000003.11:g.53847179del, NC_000003.11:g.53847179dup, NC_000003.11:g.53847178_53847179dup, NC_000003.11:g.53847177_53847179dup, NC_000003.11:g.53847175_53847179dup, NC_000003.11:g.53847157_53847179T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.53847179_53847180insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.53847179_53847180insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032999.1:g.323094_323104del, NG_032999.1:g.323095_323104del, NG_032999.1:g.323096_323104del, NG_032999.1:g.323097_323104del, NG_032999.1:g.323098_323104del, NG_032999.1:g.323099_323104del, NG_032999.1:g.323100_323104del, NG_032999.1:g.323101_323104del, NG_032999.1:g.323102_323104del, NG_032999.1:g.323103_323104del, NG_032999.1:g.323104del, NG_032999.1:g.323104dup, NG_032999.1:g.323103_323104dup, NG_032999.1:g.323102_323104dup, NG_032999.1:g.323100_323104dup, NG_032999.1:g.323082_323104T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_032999.1:g.323104_323105insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032999.1:g.323104_323105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_000720.4:c.*1736_*1746del, NM_000720.4:c.*1737_*1746del, NM_000720.4:c.*1738_*1746del, NM_000720.4:c.*1739_*1746del, NM_000720.4:c.*1740_*1746del, NM_000720.4:c.*1741_*1746del, NM_000720.4:c.*1742_*1746del, NM_000720.4:c.*1743_*1746del, NM_000720.4:c.*1744_*1746del, NM_000720.4:c.*1745_*1746del, NM_000720.4:c.*1746del, NM_000720.4:c.*1746dup, NM_000720.4:c.*1745_*1746dup, NM_000720.4:c.*1744_*1746dup, NM_000720.4:c.*1742_*1746dup, NM_000720.4:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_000720.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_000720.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128840.3:c.*1736_*1746del, NM_001128840.3:c.*1737_*1746del, NM_001128840.3:c.*1738_*1746del, NM_001128840.3:c.*1739_*1746del, NM_001128840.3:c.*1740_*1746del, NM_001128840.3:c.*1741_*1746del, NM_001128840.3:c.*1742_*1746del, NM_001128840.3:c.*1743_*1746del, NM_001128840.3:c.*1744_*1746del, NM_001128840.3:c.*1745_*1746del, NM_001128840.3:c.*1746del, NM_001128840.3:c.*1746dup, NM_001128840.3:c.*1745_*1746dup, NM_001128840.3:c.*1744_*1746dup, NM_001128840.3:c.*1742_*1746dup, NM_001128840.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001128840.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128840.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128839.3:c.*1736_*1746del, NM_001128839.3:c.*1737_*1746del, NM_001128839.3:c.*1738_*1746del, NM_001128839.3:c.*1739_*1746del, NM_001128839.3:c.*1740_*1746del, NM_001128839.3:c.*1741_*1746del, NM_001128839.3:c.*1742_*1746del, NM_001128839.3:c.*1743_*1746del, NM_001128839.3:c.*1744_*1746del, NM_001128839.3:c.*1745_*1746del, NM_001128839.3:c.*1746del, NM_001128839.3:c.*1746dup, NM_001128839.3:c.*1745_*1746dup, NM_001128839.3:c.*1744_*1746dup, NM_001128839.3:c.*1742_*1746dup, NM_001128839.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001128839.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128839.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_018397.5:c.*4637_*4647del, NM_018397.5:c.*4638_*4647del, NM_018397.5:c.*4639_*4647del, NM_018397.5:c.*4640_*4647del, NM_018397.5:c.*4641_*4647del, NM_018397.5:c.*4642_*4647del, NM_018397.5:c.*4643_*4647del, NM_018397.5:c.*4644_*4647del, NM_018397.5:c.*4645_*4647del, NM_018397.5:c.*4646_*4647del, NM_018397.5:c.*4647del, NM_018397.5:c.*4647dup, NM_018397.5:c.*4646_*4647dup, NM_018397.5:c.*4645_*4647dup, NM_018397.5:c.*4643_*4647dup, NM_018397.5:c.*4625_*4647A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NM_018397.5:c.*4647_*4648insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_018397.5:c.*4647_*4648insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005265448.4:c.*1736_*1746del, XM_005265448.4:c.*1737_*1746del, XM_005265448.4:c.*1738_*1746del, XM_005265448.4:c.*1739_*1746del, XM_005265448.4:c.*1740_*1746del, XM_005265448.4:c.*1741_*1746del, XM_005265448.4:c.*1742_*1746del, XM_005265448.4:c.*1743_*1746del, XM_005265448.4:c.*1744_*1746del, XM_005265448.4:c.*1745_*1746del, XM_005265448.4:c.*1746del, XM_005265448.4:c.*1746dup, XM_005265448.4:c.*1745_*1746dup, XM_005265448.4:c.*1744_*1746dup, XM_005265448.4:c.*1742_*1746dup, XM_005265448.4:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.2:c.*1745dup, XM_005265448.2:c.*1736_*1745del, XM_005265448.2:c.*1737_*1745del, XM_005265448.2:c.*1738_*1745del, XM_005265448.2:c.*1739_*1745del, XM_005265448.2:c.*1740_*1745del, XM_005265448.2:c.*1741_*1745del, XM_005265448.2:c.*1742_*1745del, XM_005265448.2:c.*1743_*1745del, XM_005265448.2:c.*1744_*1745del, XM_005265448.2:c.*1745del, XM_005265448.2:c.*1744_*1745dup, XM_005265448.2:c.*1743_*1745dup, XM_005265448.2:c.*1742_*1745dup, XM_005265448.2:c.*1740_*1745dup, XM_005265448.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.1:c.*1736_*1746del, XM_005265448.1:c.*1737_*1746del, XM_005265448.1:c.*1738_*1746del, XM_005265448.1:c.*1739_*1746del, XM_005265448.1:c.*1740_*1746del, XM_005265448.1:c.*1741_*1746del, XM_005265448.1:c.*1742_*1746del, XM_005265448.1:c.*1743_*1746del, XM_005265448.1:c.*1744_*1746del, XM_005265448.1:c.*1745_*1746del, XM_005265448.1:c.*1746del, XM_005265448.1:c.*1746dup, XM_005265448.1:c.*1745_*1746dup, XM_005265448.1:c.*1744_*1746dup, XM_005265448.1:c.*1742_*1746dup, XM_005265448.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.3:c.*1736_*1746del, XM_011534097.3:c.*1737_*1746del, XM_011534097.3:c.*1738_*1746del, XM_011534097.3:c.*1739_*1746del, XM_011534097.3:c.*1740_*1746del, XM_011534097.3:c.*1741_*1746del, XM_011534097.3:c.*1742_*1746del, XM_011534097.3:c.*1743_*1746del, XM_011534097.3:c.*1744_*1746del, XM_011534097.3:c.*1745_*1746del, XM_011534097.3:c.*1746del, XM_011534097.3:c.*1746dup, XM_011534097.3:c.*1745_*1746dup, XM_011534097.3:c.*1744_*1746dup, XM_011534097.3:c.*1742_*1746dup, XM_011534097.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.2:c.*1745dup, XM_011534097.2:c.*1736_*1745del, XM_011534097.2:c.*1737_*1745del, XM_011534097.2:c.*1738_*1745del, XM_011534097.2:c.*1739_*1745del, XM_011534097.2:c.*1740_*1745del, XM_011534097.2:c.*1741_*1745del, XM_011534097.2:c.*1742_*1745del, XM_011534097.2:c.*1743_*1745del, XM_011534097.2:c.*1744_*1745del, XM_011534097.2:c.*1745del, XM_011534097.2:c.*1744_*1745dup, XM_011534097.2:c.*1743_*1745dup, XM_011534097.2:c.*1742_*1745dup, XM_011534097.2:c.*1740_*1745dup, XM_011534097.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.1:c.*1745dup, XM_011534097.1:c.*1736_*1745del, XM_011534097.1:c.*1737_*1745del, XM_011534097.1:c.*1738_*1745del, XM_011534097.1:c.*1739_*1745del, XM_011534097.1:c.*1740_*1745del, XM_011534097.1:c.*1741_*1745del, XM_011534097.1:c.*1742_*1745del, XM_011534097.1:c.*1743_*1745del, XM_011534097.1:c.*1744_*1745del, XM_011534097.1:c.*1745del, XM_011534097.1:c.*1744_*1745dup, XM_011534097.1:c.*1743_*1745dup, XM_011534097.1:c.*1742_*1745dup, XM_011534097.1:c.*1740_*1745dup, XM_011534097.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.3:c.*1736_*1746del, XM_011534094.3:c.*1737_*1746del, XM_011534094.3:c.*1738_*1746del, XM_011534094.3:c.*1739_*1746del, XM_011534094.3:c.*1740_*1746del, XM_011534094.3:c.*1741_*1746del, XM_011534094.3:c.*1742_*1746del, XM_011534094.3:c.*1743_*1746del, XM_011534094.3:c.*1744_*1746del, XM_011534094.3:c.*1745_*1746del, XM_011534094.3:c.*1746del, XM_011534094.3:c.*1746dup, XM_011534094.3:c.*1745_*1746dup, XM_011534094.3:c.*1744_*1746dup, XM_011534094.3:c.*1742_*1746dup, XM_011534094.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.2:c.*1745dup, XM_011534094.2:c.*1736_*1745del, XM_011534094.2:c.*1737_*1745del, XM_011534094.2:c.*1738_*1745del, XM_011534094.2:c.*1739_*1745del, XM_011534094.2:c.*1740_*1745del, XM_011534094.2:c.*1741_*1745del, XM_011534094.2:c.*1742_*1745del, XM_011534094.2:c.*1743_*1745del, XM_011534094.2:c.*1744_*1745del, XM_011534094.2:c.*1745del, XM_011534094.2:c.*1744_*1745dup, XM_011534094.2:c.*1743_*1745dup, XM_011534094.2:c.*1742_*1745dup, XM_011534094.2:c.*1740_*1745dup, XM_011534094.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.1:c.*1745dup, XM_011534094.1:c.*1736_*1745del, XM_011534094.1:c.*1737_*1745del, XM_011534094.1:c.*1738_*1745del, XM_011534094.1:c.*1739_*1745del, XM_011534094.1:c.*1740_*1745del, XM_011534094.1:c.*1741_*1745del, XM_011534094.1:c.*1742_*1745del, XM_011534094.1:c.*1743_*1745del, XM_011534094.1:c.*1744_*1745del, XM_011534094.1:c.*1745del, XM_011534094.1:c.*1744_*1745dup, XM_011534094.1:c.*1743_*1745dup, XM_011534094.1:c.*1742_*1745dup, XM_011534094.1:c.*1740_*1745dup, XM_011534094.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.3:c.*1736_*1746del, XM_011534100.3:c.*1737_*1746del, XM_011534100.3:c.*1738_*1746del, XM_011534100.3:c.*1739_*1746del, XM_011534100.3:c.*1740_*1746del, XM_011534100.3:c.*1741_*1746del, XM_011534100.3:c.*1742_*1746del, XM_011534100.3:c.*1743_*1746del, XM_011534100.3:c.*1744_*1746del, XM_011534100.3:c.*1745_*1746del, XM_011534100.3:c.*1746del, XM_011534100.3:c.*1746dup, XM_011534100.3:c.*1745_*1746dup, XM_011534100.3:c.*1744_*1746dup, XM_011534100.3:c.*1742_*1746dup, XM_011534100.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.2:c.*1745dup, XM_011534100.2:c.*1736_*1745del, XM_011534100.2:c.*1737_*1745del, XM_011534100.2:c.*1738_*1745del, XM_011534100.2:c.*1739_*1745del, XM_011534100.2:c.*1740_*1745del, XM_011534100.2:c.*1741_*1745del, XM_011534100.2:c.*1742_*1745del, XM_011534100.2:c.*1743_*1745del, XM_011534100.2:c.*1744_*1745del, XM_011534100.2:c.*1745del, XM_011534100.2:c.*1744_*1745dup, XM_011534100.2:c.*1743_*1745dup, XM_011534100.2:c.*1742_*1745dup, XM_011534100.2:c.*1740_*1745dup, XM_011534100.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.1:c.*1745dup, XM_011534100.1:c.*1736_*1745del, XM_011534100.1:c.*1737_*1745del, XM_011534100.1:c.*1738_*1745del, XM_011534100.1:c.*1739_*1745del, XM_011534100.1:c.*1740_*1745del, XM_011534100.1:c.*1741_*1745del, XM_011534100.1:c.*1742_*1745del, XM_011534100.1:c.*1743_*1745del, XM_011534100.1:c.*1744_*1745del, XM_011534100.1:c.*1745del, XM_011534100.1:c.*1744_*1745dup, XM_011534100.1:c.*1743_*1745dup, XM_011534100.1:c.*1742_*1745dup, XM_011534100.1:c.*1740_*1745dup, XM_011534100.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.3:c.*1736_*1746del, XM_011534096.3:c.*1737_*1746del, XM_011534096.3:c.*1738_*1746del, XM_011534096.3:c.*1739_*1746del, XM_011534096.3:c.*1740_*1746del, XM_011534096.3:c.*1741_*1746del, XM_011534096.3:c.*1742_*1746del, XM_011534096.3:c.*1743_*1746del, XM_011534096.3:c.*1744_*1746del, XM_011534096.3:c.*1745_*1746del, XM_011534096.3:c.*1746del, XM_011534096.3:c.*1746dup, XM_011534096.3:c.*1745_*1746dup, XM_011534096.3:c.*1744_*1746dup, XM_011534096.3:c.*1742_*1746dup, XM_011534096.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534096.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.1:c.*1745dup, XM_011534096.1:c.*1736_*1745del, XM_011534096.1:c.*1737_*1745del, XM_011534096.1:c.*1738_*1745del, XM_011534096.1:c.*1739_*1745del, XM_011534096.1:c.*1740_*1745del, XM_011534096.1:c.*1741_*1745del, XM_011534096.1:c.*1742_*1745del, XM_011534096.1:c.*1743_*1745del, XM_011534096.1:c.*1744_*1745del, XM_011534096.1:c.*1745del, XM_011534096.1:c.*1744_*1745dup, XM_011534096.1:c.*1743_*1745dup, XM_011534096.1:c.*1742_*1745dup, XM_011534096.1:c.*1740_*1745dup, XM_011534096.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534096.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.3:c.*1736_*1746del, XM_011534099.3:c.*1737_*1746del, XM_011534099.3:c.*1738_*1746del, XM_011534099.3:c.*1739_*1746del, XM_011534099.3:c.*1740_*1746del, XM_011534099.3:c.*1741_*1746del, XM_011534099.3:c.*1742_*1746del, XM_011534099.3:c.*1743_*1746del, XM_011534099.3:c.*1744_*1746del, XM_011534099.3:c.*1745_*1746del, XM_011534099.3:c.*1746del, XM_011534099.3:c.*1746dup, XM_011534099.3:c.*1745_*1746dup, XM_011534099.3:c.*1744_*1746dup, XM_011534099.3:c.*1742_*1746dup, XM_011534099.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.2:c.*1745dup, XM_011534099.2:c.*1736_*1745del, XM_011534099.2:c.*1737_*1745del, XM_011534099.2:c.*1738_*1745del, XM_011534099.2:c.*1739_*1745del, XM_011534099.2:c.*1740_*1745del, XM_011534099.2:c.*1741_*1745del, XM_011534099.2:c.*1742_*1745del, XM_011534099.2:c.*1743_*1745del, XM_011534099.2:c.*1744_*1745del, XM_011534099.2:c.*1745del, XM_011534099.2:c.*1744_*1745dup, XM_011534099.2:c.*1743_*1745dup, XM_011534099.2:c.*1742_*1745dup, XM_011534099.2:c.*1740_*1745dup, XM_011534099.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.1:c.*1745dup, XM_011534099.1:c.*1736_*1745del, XM_011534099.1:c.*1737_*1745del, XM_011534099.1:c.*1738_*1745del, XM_011534099.1:c.*1739_*1745del, XM_011534099.1:c.*1740_*1745del, XM_011534099.1:c.*1741_*1745del, XM_011534099.1:c.*1742_*1745del, XM_011534099.1:c.*1743_*1745del, XM_011534099.1:c.*1744_*1745del, XM_011534099.1:c.*1745del, XM_011534099.1:c.*1744_*1745dup, XM_011534099.1:c.*1743_*1745dup, XM_011534099.1:c.*1742_*1745dup, XM_011534099.1:c.*1740_*1745dup, XM_011534099.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.2:c.*1736_*1746del, XM_017007137.2:c.*1737_*1746del, XM_017007137.2:c.*1738_*1746del, XM_017007137.2:c.*1739_*1746del, XM_017007137.2:c.*1740_*1746del, XM_017007137.2:c.*1741_*1746del, XM_017007137.2:c.*1742_*1746del, XM_017007137.2:c.*1743_*1746del, XM_017007137.2:c.*1744_*1746del, XM_017007137.2:c.*1745_*1746del, XM_017007137.2:c.*1746del, XM_017007137.2:c.*1746dup, XM_017007137.2:c.*1745_*1746dup, XM_017007137.2:c.*1744_*1746dup, XM_017007137.2:c.*1742_*1746dup, XM_017007137.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007137.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.1:c.*1745dup, XM_017007137.1:c.*1736_*1745del, XM_017007137.1:c.*1737_*1745del, XM_017007137.1:c.*1738_*1745del, XM_017007137.1:c.*1739_*1745del, XM_017007137.1:c.*1740_*1745del, XM_017007137.1:c.*1741_*1745del, XM_017007137.1:c.*1742_*1745del, XM_017007137.1:c.*1743_*1745del, XM_017007137.1:c.*1744_*1745del, XM_017007137.1:c.*1745del, XM_017007137.1:c.*1744_*1745dup, XM_017007137.1:c.*1743_*1745dup, XM_017007137.1:c.*1742_*1745dup, XM_017007137.1:c.*1740_*1745dup, XM_017007137.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007137.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.2:c.*1736_*1746del, XM_017007138.2:c.*1737_*1746del, XM_017007138.2:c.*1738_*1746del, XM_017007138.2:c.*1739_*1746del, XM_017007138.2:c.*1740_*1746del, XM_017007138.2:c.*1741_*1746del, XM_017007138.2:c.*1742_*1746del, XM_017007138.2:c.*1743_*1746del, XM_017007138.2:c.*1744_*1746del, XM_017007138.2:c.*1745_*1746del, XM_017007138.2:c.*1746del, XM_017007138.2:c.*1746dup, XM_017007138.2:c.*1745_*1746dup, XM_017007138.2:c.*1744_*1746dup, XM_017007138.2:c.*1742_*1746dup, XM_017007138.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007138.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.1:c.*1745dup, XM_017007138.1:c.*1736_*1745del, XM_017007138.1:c.*1737_*1745del, XM_017007138.1:c.*1738_*1745del, XM_017007138.1:c.*1739_*1745del, XM_017007138.1:c.*1740_*1745del, XM_017007138.1:c.*1741_*1745del, XM_017007138.1:c.*1742_*1745del, XM_017007138.1:c.*1743_*1745del, XM_017007138.1:c.*1744_*1745del, XM_017007138.1:c.*1745del, XM_017007138.1:c.*1744_*1745dup, XM_017007138.1:c.*1743_*1745dup, XM_017007138.1:c.*1742_*1745dup, XM_017007138.1:c.*1740_*1745dup, XM_017007138.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007138.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.2:c.*1736_*1746del, XM_017007139.2:c.*1737_*1746del, XM_017007139.2:c.*1738_*1746del, XM_017007139.2:c.*1739_*1746del, XM_017007139.2:c.*1740_*1746del, XM_017007139.2:c.*1741_*1746del, XM_017007139.2:c.*1742_*1746del, XM_017007139.2:c.*1743_*1746del, XM_017007139.2:c.*1744_*1746del, XM_017007139.2:c.*1745_*1746del, XM_017007139.2:c.*1746del, XM_017007139.2:c.*1746dup, XM_017007139.2:c.*1745_*1746dup, XM_017007139.2:c.*1744_*1746dup, XM_017007139.2:c.*1742_*1746dup, XM_017007139.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007139.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.1:c.*1745dup, XM_017007139.1:c.*1736_*1745del, XM_017007139.1:c.*1737_*1745del, XM_017007139.1:c.*1738_*1745del, XM_017007139.1:c.*1739_*1745del, XM_017007139.1:c.*1740_*1745del, XM_017007139.1:c.*1741_*1745del, XM_017007139.1:c.*1742_*1745del, XM_017007139.1:c.*1743_*1745del, XM_017007139.1:c.*1744_*1745del, XM_017007139.1:c.*1745del, XM_017007139.1:c.*1744_*1745dup, XM_017007139.1:c.*1743_*1745dup, XM_017007139.1:c.*1742_*1745dup, XM_017007139.1:c.*1740_*1745dup, XM_017007139.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007139.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.2:c.*1736_*1746del, XM_017007141.2:c.*1737_*1746del, XM_017007141.2:c.*1738_*1746del, XM_017007141.2:c.*1739_*1746del, XM_017007141.2:c.*1740_*1746del, XM_017007141.2:c.*1741_*1746del, XM_017007141.2:c.*1742_*1746del, XM_017007141.2:c.*1743_*1746del, XM_017007141.2:c.*1744_*1746del, XM_017007141.2:c.*1745_*1746del, XM_017007141.2:c.*1746del, XM_017007141.2:c.*1746dup, XM_017007141.2:c.*1745_*1746dup, XM_017007141.2:c.*1744_*1746dup, XM_017007141.2:c.*1742_*1746dup, XM_017007141.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007141.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.1:c.*1745dup, XM_017007141.1:c.*1736_*1745del, XM_017007141.1:c.*1737_*1745del, XM_017007141.1:c.*1738_*1745del, XM_017007141.1:c.*1739_*1745del, XM_017007141.1:c.*1740_*1745del, XM_017007141.1:c.*1741_*1745del, XM_017007141.1:c.*1742_*1745del, XM_017007141.1:c.*1743_*1745del, XM_017007141.1:c.*1744_*1745del, XM_017007141.1:c.*1745del, XM_017007141.1:c.*1744_*1745dup, XM_017007141.1:c.*1743_*1745dup, XM_017007141.1:c.*1742_*1745dup, XM_017007141.1:c.*1740_*1745dup, XM_017007141.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007141.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.2:c.*1736_*1746del, XM_017007140.2:c.*1737_*1746del, XM_017007140.2:c.*1738_*1746del, XM_017007140.2:c.*1739_*1746del, XM_017007140.2:c.*1740_*1746del, XM_017007140.2:c.*1741_*1746del, XM_017007140.2:c.*1742_*1746del, XM_017007140.2:c.*1743_*1746del, XM_017007140.2:c.*1744_*1746del, XM_017007140.2:c.*1745_*1746del, XM_017007140.2:c.*1746del, XM_017007140.2:c.*1746dup, XM_017007140.2:c.*1745_*1746dup, XM_017007140.2:c.*1744_*1746dup, XM_017007140.2:c.*1742_*1746dup, XM_017007140.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007140.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.1:c.*1745dup, XM_017007140.1:c.*1736_*1745del, XM_017007140.1:c.*1737_*1745del, XM_017007140.1:c.*1738_*1745del, XM_017007140.1:c.*1739_*1745del, XM_017007140.1:c.*1740_*1745del, XM_017007140.1:c.*1741_*1745del, XM_017007140.1:c.*1742_*1745del, XM_017007140.1:c.*1743_*1745del, XM_017007140.1:c.*1744_*1745del, XM_017007140.1:c.*1745del, XM_017007140.1:c.*1744_*1745dup, XM_017007140.1:c.*1743_*1745dup, XM_017007140.1:c.*1742_*1745dup, XM_017007140.1:c.*1740_*1745dup, XM_017007140.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007140.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007144.2:c.*1736_*1746del, XM_017007144.2:c.*1737_*1746del, XM_017007144.2:c.*1738_*1746del, XM_017007144.2:c.*1739_*1746del, XM_017007144.2:c.*1740_*1746del, XM_017007144.2:c.*1741_*1746del, XM_017007144.2:c.*1742_*1746del, XM_017007144.2:c.*1743_*1746del, XM_017007144.2:c.*1744_*1746del, XM_017007144.2:c.*1745_*1746del, XM_017007144.2:c.*1746del, XM_017007144.2:c.*1746dup, XM_017007144.2:c.*1745_*1746dup, XM_017007144.2:c.*1744_*1746dup, XM_017007144.2:c.*1742_*1746dup, XM_017007144.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007144.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007144.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.2:c.*1736_*1746del, XM_017007143.2:c.*1737_*1746del, XM_017007143.2:c.*1738_*1746del, XM_017007143.2:c.*1739_*1746del, XM_017007143.2:c.*1740_*1746del, XM_017007143.2:c.*1741_*1746del, XM_017007143.2:c.*1742_*1746del, XM_017007143.2:c.*1743_*1746del, XM_017007143.2:c.*1744_*1746del, XM_017007143.2:c.*1745_*1746del, XM_017007143.2:c.*1746del, XM_017007143.2:c.*1746dup, XM_017007143.2:c.*1745_*1746dup, XM_017007143.2:c.*1744_*1746dup, XM_017007143.2:c.*1742_*1746dup, XM_017007143.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007143.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.1:c.*1745dup, XM_017007143.1:c.*1736_*1745del, XM_017007143.1:c.*1737_*1745del, XM_017007143.1:c.*1738_*1745del, XM_017007143.1:c.*1739_*1745del, XM_017007143.1:c.*1740_*1745del, XM_017007143.1:c.*1741_*1745del, XM_017007143.1:c.*1742_*1745del, XM_017007143.1:c.*1743_*1745del, XM_017007143.1:c.*1744_*1745del, XM_017007143.1:c.*1745del, XM_017007143.1:c.*1744_*1745dup, XM_017007143.1:c.*1743_*1745dup, XM_017007143.1:c.*1742_*1745dup, XM_017007143.1:c.*1740_*1745dup, XM_017007143.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007143.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.2:c.*1736_*1746del, XM_017007142.2:c.*1737_*1746del, XM_017007142.2:c.*1738_*1746del, XM_017007142.2:c.*1739_*1746del, XM_017007142.2:c.*1740_*1746del, XM_017007142.2:c.*1741_*1746del, XM_017007142.2:c.*1742_*1746del, XM_017007142.2:c.*1743_*1746del, XM_017007142.2:c.*1744_*1746del, XM_017007142.2:c.*1745_*1746del, XM_017007142.2:c.*1746del, XM_017007142.2:c.*1746dup, XM_017007142.2:c.*1745_*1746dup, XM_017007142.2:c.*1744_*1746dup, XM_017007142.2:c.*1742_*1746dup, XM_017007142.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007142.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.1:c.*1745dup, XM_017007142.1:c.*1736_*1745del, XM_017007142.1:c.*1737_*1745del, XM_017007142.1:c.*1738_*1745del, XM_017007142.1:c.*1739_*1745del, XM_017007142.1:c.*1740_*1745del, XM_017007142.1:c.*1741_*1745del, XM_017007142.1:c.*1742_*1745del, XM_017007142.1:c.*1743_*1745del, XM_017007142.1:c.*1744_*1745del, XM_017007142.1:c.*1745del, XM_017007142.1:c.*1744_*1745dup, XM_017007142.1:c.*1743_*1745dup, XM_017007142.1:c.*1742_*1745dup, XM_017007142.1:c.*1740_*1745dup, XM_017007142.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007142.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.2:c.*1736_*1746del, XM_017007145.2:c.*1737_*1746del, XM_017007145.2:c.*1738_*1746del, XM_017007145.2:c.*1739_*1746del, XM_017007145.2:c.*1740_*1746del, XM_017007145.2:c.*1741_*1746del, XM_017007145.2:c.*1742_*1746del, XM_017007145.2:c.*1743_*1746del, XM_017007145.2:c.*1744_*1746del, XM_017007145.2:c.*1745_*1746del, XM_017007145.2:c.*1746del, XM_017007145.2:c.*1746dup, XM_017007145.2:c.*1745_*1746dup, XM_017007145.2:c.*1744_*1746dup, XM_017007145.2:c.*1742_*1746dup, XM_017007145.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007145.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.1:c.*1745dup, XM_017007145.1:c.*1736_*1745del, XM_017007145.1:c.*1737_*1745del, XM_017007145.1:c.*1738_*1745del, XM_017007145.1:c.*1739_*1745del, XM_017007145.1:c.*1740_*1745del, XM_017007145.1:c.*1741_*1745del, XM_017007145.1:c.*1742_*1745del, XM_017007145.1:c.*1743_*1745del, XM_017007145.1:c.*1744_*1745del, XM_017007145.1:c.*1745del, XM_017007145.1:c.*1744_*1745dup, XM_017007145.1:c.*1743_*1745dup, XM_017007145.1:c.*1742_*1745dup, XM_017007145.1:c.*1740_*1745dup, XM_017007145.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007145.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448871.1:c.*1736_*1746del, XM_047448871.1:c.*1737_*1746del, XM_047448871.1:c.*1738_*1746del, XM_047448871.1:c.*1739_*1746del, XM_047448871.1:c.*1740_*1746del, XM_047448871.1:c.*1741_*1746del, XM_047448871.1:c.*1742_*1746del, XM_047448871.1:c.*1743_*1746del, XM_047448871.1:c.*1744_*1746del, XM_047448871.1:c.*1745_*1746del, XM_047448871.1:c.*1746del, XM_047448871.1:c.*1746dup, XM_047448871.1:c.*1745_*1746dup, XM_047448871.1:c.*1744_*1746dup, XM_047448871.1:c.*1742_*1746dup, XM_047448871.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047448871.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448871.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448872.1:c.*1736_*1746del, XM_047448872.1:c.*1737_*1746del, XM_047448872.1:c.*1738_*1746del, XM_047448872.1:c.*1739_*1746del, XM_047448872.1:c.*1740_*1746del, XM_047448872.1:c.*1741_*1746del, XM_047448872.1:c.*1742_*1746del, XM_047448872.1:c.*1743_*1746del, XM_047448872.1:c.*1744_*1746del, XM_047448872.1:c.*1745_*1746del, XM_047448872.1:c.*1746del, XM_047448872.1:c.*1746dup, XM_047448872.1:c.*1745_*1746dup, XM_047448872.1:c.*1744_*1746dup, XM_047448872.1:c.*1742_*1746dup, XM_047448872.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047448872.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448872.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              7.

              rs1491080246 has merged into rs34884918 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT [Show Flanks]
                Chromosome:
                3:53830416 (GRCh38)
                3:53864443 (GRCh37)
                Canonical SPDI:
                NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT
                Gene:
                CHDH (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TATATATATATATAT=0./0 (ALFA)
                TA=0.21486/1076 (1000Genomes)
                HGVS:
                NC_000003.12:g.53830404AT[6], NC_000003.12:g.53830404AT[7], NC_000003.12:g.53830404AT[8], NC_000003.12:g.53830404AT[10], NC_000003.12:g.53830404AT[11], NC_000003.12:g.53830404AT[12], NC_000003.12:g.53830404AT[13], NC_000003.12:g.53830404AT[14], NC_000003.12:g.53830404AT[15], NC_000003.12:g.53830404AT[16], NC_000003.12:g.53830404AT[17], NC_000003.12:g.53830404AT[18], NC_000003.12:g.53830404AT[19], NC_000003.11:g.53864431AT[6], NC_000003.11:g.53864431AT[7], NC_000003.11:g.53864431AT[8], NC_000003.11:g.53864431AT[10], NC_000003.11:g.53864431AT[11], NC_000003.11:g.53864431AT[12], NC_000003.11:g.53864431AT[13], NC_000003.11:g.53864431AT[14], NC_000003.11:g.53864431AT[15], NC_000003.11:g.53864431AT[16], NC_000003.11:g.53864431AT[17], NC_000003.11:g.53864431AT[18], NC_000003.11:g.53864431AT[19], NG_028042.1:g.20974TA[6], NG_028042.1:g.20974TA[7], NG_028042.1:g.20974TA[8], NG_028042.1:g.20974TA[10], NG_028042.1:g.20974TA[11], NG_028042.1:g.20974TA[12], NG_028042.1:g.20974TA[13], NG_028042.1:g.20974TA[14], NG_028042.1:g.20974TA[15], NG_028042.1:g.20974TA[16], NG_028042.1:g.20974TA[17], NG_028042.1:g.20974TA[18], NG_028042.1:g.20974TA[19]
                8.

                rs1491061443 has merged into rs59355780 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                  Chromosome:
                  3:53826326 (GRCh38)
                  3:53860353 (GRCh37)
                  Canonical SPDI:
                  NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                  Gene:
                  CHDH (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAAAAAAAA=0./0 (ALFA)
                  -=0.15/6 (GENOME_DK)
                  A=0.23734/389 (1000Genomes)
                  HGVS:
                  9.

                  rs1490942604 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>C [Show Flanks]
                    Chromosome:
                    3:53819141 (GRCh38)
                    3:53853168 (GRCh37)
                    Canonical SPDI:
                    NC_000003.12:53819140:A:C
                    Gene:
                    CHDH (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000004/1 (TOPMED)
                    C=0.000007/1 (GnomAD)
                    HGVS:
                    10.

                    rs1490858221 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      3:53834678 (GRCh38)
                      3:53868705 (GRCh37)
                      Canonical SPDI:
                      NC_000003.12:53834677:G:A
                      Gene:
                      CHDH (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000007/1 (GnomAD)
                      A=0.000011/3 (TOPMED)
                      HGVS:
                      11.

                      rs1490823672 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A,T [Show Flanks]
                        Chromosome:
                        3:53842030 (GRCh38)
                        3:53876057 (GRCh37)
                        Canonical SPDI:
                        NC_000003.12:53842029:C:A,NC_000003.12:53842029:C:T
                        Gene:
                        CHDH (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000019/5 (TOPMED)
                        HGVS:
                        12.

                        rs1490783693 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          3:53827279 (GRCh38)
                          3:53861306 (GRCh37)
                          Canonical SPDI:
                          NC_000003.12:53827278:C:T
                          Gene:
                          CHDH (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000011/3 (TOPMED)
                          T=0.000106/3 (TOMMO)
                          HGVS:
                          13.

                          rs1490663464 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            3:53832486 (GRCh38)
                            3:53866513 (GRCh37)
                            Canonical SPDI:
                            NC_000003.12:53832485:C:T
                            Gene:
                            CHDH (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000007/1 (GnomAD)
                            T=0.000019/5 (TOPMED)
                            HGVS:
                            14.

                            rs1490581879 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TT>- [Show Flanks]
                              Chromosome:
                              3:53812885 (GRCh38)
                              3:53846912 (GRCh37)
                              Canonical SPDI:
                              NC_000003.12:53812883:TTT:T
                              Gene:
                              CACNA1D (Varview), CHDH (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,3_prime_UTR_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              -=0.000029/4 (GnomAD)
                              -=0.000042/11 (TOPMED)
                              HGVS:
                              NC_000003.12:g.53812885_53812886del, NC_000003.11:g.53846912_53846913del, NG_032999.1:g.322837_322838del, NM_000720.4:c.*1479_*1480del, NM_001128840.3:c.*1479_*1480del, NM_001128839.3:c.*1479_*1480del, NM_018397.5:c.*4892_*4893del, XM_005265448.4:c.*1479_*1480del, XM_005265448.2:c.*1479_*1480del, XM_005265448.1:c.*1479_*1480del, XM_011534097.3:c.*1479_*1480del, XM_011534097.2:c.*1479_*1480del, XM_011534097.1:c.*1479_*1480del, XM_011534094.3:c.*1479_*1480del, XM_011534094.2:c.*1479_*1480del, XM_011534094.1:c.*1479_*1480del, XM_011534100.3:c.*1479_*1480del, XM_011534100.2:c.*1479_*1480del, XM_011534100.1:c.*1479_*1480del, XM_011534096.3:c.*1479_*1480del, XM_011534096.1:c.*1479_*1480del, XM_011534099.3:c.*1479_*1480del, XM_011534099.2:c.*1479_*1480del, XM_011534099.1:c.*1479_*1480del, XM_017007137.2:c.*1479_*1480del, XM_017007137.1:c.*1479_*1480del, XM_017007138.2:c.*1479_*1480del, XM_017007138.1:c.*1479_*1480del, XM_017007139.2:c.*1479_*1480del, XM_017007139.1:c.*1479_*1480del, XM_017007141.2:c.*1479_*1480del, XM_017007141.1:c.*1479_*1480del, XM_017007140.2:c.*1479_*1480del, XM_017007140.1:c.*1479_*1480del, XM_017007144.2:c.*1479_*1480del, XM_017007143.2:c.*1479_*1480del, XM_017007143.1:c.*1479_*1480del, XM_017007142.2:c.*1479_*1480del, XM_017007142.1:c.*1479_*1480del, XM_017007145.2:c.*1479_*1480del, XM_017007145.1:c.*1479_*1480del, XM_047448871.1:c.*1479_*1480del, XM_047448872.1:c.*1479_*1480del
                              15.

                              rs1490573910 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                3:53826133 (GRCh38)
                                3:53860160 (GRCh37)
                                Canonical SPDI:
                                NC_000003.12:53826132:A:G
                                Gene:
                                CHDH (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000004/1 (TOPMED)
                                HGVS:
                                16.

                                rs1490495720 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>T [Show Flanks]
                                  Chromosome:
                                  3:53833163 (GRCh38)
                                  3:53867190 (GRCh37)
                                  Canonical SPDI:
                                  NC_000003.12:53833162:G:T
                                  Gene:
                                  CHDH (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  T=0.000015/4 (TOPMED)
                                  HGVS:
                                  17.

                                  rs1490426902 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    3:53847947 (GRCh38)
                                    3:53881974 (GRCh37)
                                    Canonical SPDI:
                                    NC_000003.12:53847946:T:C
                                    Gene:
                                    CHDH (Varview), IL17RB (Varview)
                                    Functional Consequence:
                                    intron_variant,upstream_transcript_variant,2KB_upstream_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0./0 (ALFA)
                                    C=0.000007/1 (GnomAD)
                                    C=0.000008/2 (TOPMED)
                                    HGVS:
                                    19.

                                    rs1490222354 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ->T [Show Flanks]
                                      Chromosome:
                                      3:53812761 (GRCh38)
                                      3:53846789 (GRCh37)
                                      Canonical SPDI:
                                      NC_000003.12:53812761:T:TT
                                      Gene:
                                      CACNA1D (Varview), CHDH (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,3_prime_UTR_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TT=0./0 (ALFA)
                                      T=0.000007/1 (GnomAD)
                                      T=0.000042/11 (TOPMED)
                                      HGVS:
                                      NC_000003.12:g.53812762dup, NC_000003.11:g.53846789dup, NG_032999.1:g.322714dup, NM_000720.4:c.*1356dup, NM_001128840.3:c.*1356dup, NM_001128839.3:c.*1356dup, NM_018397.5:c.*5015dup, XM_005265448.4:c.*1356dup, XM_005265448.2:c.*1356dup, XM_005265448.1:c.*1356dup, XM_011534097.3:c.*1356dup, XM_011534097.2:c.*1356dup, XM_011534097.1:c.*1356dup, XM_011534094.3:c.*1356dup, XM_011534094.2:c.*1356dup, XM_011534094.1:c.*1356dup, XM_011534100.3:c.*1356dup, XM_011534100.2:c.*1356dup, XM_011534100.1:c.*1356dup, XM_011534096.3:c.*1356dup, XM_011534096.1:c.*1356dup, XM_011534099.3:c.*1356dup, XM_011534099.2:c.*1356dup, XM_011534099.1:c.*1356dup, XM_017007137.2:c.*1356dup, XM_017007137.1:c.*1356dup, XM_017007138.2:c.*1356dup, XM_017007138.1:c.*1356dup, XM_017007139.2:c.*1356dup, XM_017007139.1:c.*1356dup, XM_017007141.2:c.*1356dup, XM_017007141.1:c.*1356dup, XM_017007140.2:c.*1356dup, XM_017007140.1:c.*1356dup, XM_017007144.2:c.*1356dup, XM_017007143.2:c.*1356dup, XM_017007143.1:c.*1356dup, XM_017007142.2:c.*1356dup, XM_017007142.1:c.*1356dup, XM_017007145.2:c.*1356dup, XM_017007145.1:c.*1356dup, XM_047448871.1:c.*1356dup, XM_047448872.1:c.*1356dup
                                      20.

                                      rs1490214138 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A [Show Flanks]
                                        Chromosome:
                                        3:53844984 (GRCh38)
                                        3:53879011 (GRCh37)
                                        Canonical SPDI:
                                        NC_000003.12:53844983:C:A
                                        Gene:
                                        CHDH (Varview), IL17RB (Varview)
                                        Functional Consequence:
                                        intron_variant,upstream_transcript_variant,2KB_upstream_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        HGVS:

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