SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2696 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216884 | GAGGTGGGAGGAGGG[C/G]AGAAGTGAAGGAAGA | 50717 |
rs750936 | snp | A/G | 0.489608 | 0.0713316 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237740 | AGATGGGGTCTTGCT[A/G]TATTGCCCAGGCTGG | 50717 |
rs756311 | snp | A/T | 0.439918 | 0.162576 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235050 | GTAAAATATAAATTA[A/T]TTTATATTGGGGAAT | 50717 |
rs947492 | snp | A/G | 0.497359 | 0.0362457 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246738 | TGCCTCGGCCTCCCA[A/G]TGTGCTGGGATTATA | 50717 |
rs947493 | snp | C/T | 0.442113 | 0.159977 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246404 | TTTAATTCTACTTAC[C/T]TTTATCATCTGTGCA | 50717 |
rs947494 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263016 | TTTACCCACACCACC[C/T]CTCTTCAGAAAAGAG | 50717 |
rs947495 | snp | C/T | 0.441841 | 0.160303 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262886 | CTTAAGGAAACAAAG[C/T]CCTGAAAGGAAACGG | 50717 |
rs947496 | snp | A/T | 0.441568 | 0.160629 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262716 | AACTCGCATTTGTTT[A/T]GAGTATCACAAGATA | 50717 |
rs1053553 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216900 | GAGGGAGGCTGGGAA[A/G]AGGTGGGAGGAGGGG | 50717 |
rs1053572 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160215998 | CACAAGATCCAACCA[A/G]GAATTCTGTATCCTG | 50717 |
rs1061511 | snp | G/T | 0.43978 | 0.162738 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219710 | AAGGCCTGCCTGCTG[G/T]AGTTTATTTCTTTTG | 50717 |
rs1132881 | snp | A/G | 0.126564 | 0.217402 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216505 | TTTGGTGTAGGGGTT[A/G]GGAAAAACAGGAAAT | 50717 |
rs1134572 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217929 | ATTGGCTTGCAGCCA[C/T]ACCCATTCTGTGTAT | 50717 |
rs1139189 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253419 | ttgggaggccaaggc[A/G]ggtggatcgcctgag | 50717 |
rs1539245 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228127 | agacacagtcttgct[A/T]tattgcccaagttgg | 50717 |
rs1573013 | snp | C/G | 0.442249 | 0.159814 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231716 | TTACTGTGTTGGACT[C/G]CAGCTAAACTGAGGC | 50717 |
rs1815703 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245904 | TGATCTGCCCTCCTC[A/G]GCCTCCCAAAGTGCT | 50717 |
rs2096144 | snp | C/G | 0.441977 | 0.16014 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246905 | GTGGTATAATCACAG[C/G]TCACTGCAGCCTCAA | 50717 |
rs2275700 | snp | A/G | 0.441705 | 0.160466 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244237 | CCTCCCCAAAAATAT[A/G]TCATTATATGGATTT | 50717 |
rs2275701 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238850 | GTTTCCAGCTGTCAT[A/G]TAAGAAAAGGGGGTA | 50717 |
rs2275702 | snp | A/G | 0.017689 | 0.0923665 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160238649 | CACACAGTGTTGCAA[A/G]AATACAAAACGTGTG | 50717 |
rs2369473 | snp | A/C | 0.488606 | 0.0746142 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240937 | TGGGAGGCCGAGGCA[A/C]GTGGATCACGAGGTT | 50717 |
rs3189630 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215309 | CCCCTATCTTGTGCT[C/T]TTCTGTCTGCAGTGT | 50717 |
rs3747624 | snp | A/G | 0.0177 | 0.0923944 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231455 | ACTCCAAAAGATCCA[A/G]ATGGTCATGGCAAAG | 50717 |
rs3898317 | snp | A/G | 0.489024 | 0.0732638 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264364 | GGGTTGGGAGCATAG[A/G]AGGAGGGGAGAGACA | 50717 |
rs4535996 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216348 | tCTTCTGTCACAAAG[A/T]ACCACAATAGTCTGC | 50717 |
rs4596880 | snp | A/T | 0.488485 | 0.0749998 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254910 | CCACCTGCTTTTGAG[A/T]TTTTCTTTTGTAAAA | 50717 |
rs4656252 | snp | A/G | 0.120326 | 0.21374 | downstream-variant-500B | PEA15, DCAF8 | GRCh38.p7 | 1:160215472 | CCCAGAATAAGGGCT[A/G]GGAAAATACCCCAAG | 50717 |
rs4656892 | snp | A/G | 0.444133 | 0.157519 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250423 | gtgagccaagatcgc[A/G]ccattgcactccagc | 50717 |
rs4656893 | snp | A/C | 0.0341735 | 0.126361 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250652 | TCTCACTTGAAAACG[A/C]AAGTGCTGAAAGGAT | 50717 |
rs6663516 | snp | G/T | 0.126909 | 0.217598 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263510 | ccggcatggtggagc[G/T]cgcctgcaatcccag | 50717 |
rs6670084 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247703 | catcaagttggcatt[C/T]gaaaagtttcagatt | 50717 |
rs6675318 | snp | A/C | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224046 | CCTCTTCTGCCTCAT[A/C]TAAAAGAATTGTTTA | 50717 |
rs6683068 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244310 | TGATTTTTCAGATGC[A/G]AAAGTGGGAACTAAA | 50717 |
rs6683177 | snp | A/G | 0.14665 | 0.227637 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244423 | AGCATTGCCCCCTAG[A/G]CAAGAATCTTCCAAT | 50717 |
rs6686429 | snp | C/T | 0.126564 | 0.217402 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258430 | CCACTCTAATCATCC[C/T]AGGAAATACTACCTA | 50717 |
rs6687974 | snp | A/G | 0.441568 | 0.160629 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254183 | AAAAATAAGCTAGGT[A/G]TGGTGGTGCATGCCT | 50717 |
rs6688586 | snp | A/C | 0.489259 | 0.0724914 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263555 | gaggcaggagaattg[A/C]ttgaacccggaggcg | 50717 |
rs6690637 | snp | A/C | 0.441568 | 0.160629 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260466 | CCAGTGTCACTCAAT[A/C]TTTTCCTACTACAAA | 50717 |
rs6701228 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260071 | AACTTATTCAAAGCT[C/G]TATCAATGATGTGCA | 50717 |
rs6703880 | snp | A/C | 0.440057 | 0.162414 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263930 | gtccatcTACTAGAT[A/C]TTTACTAGACTTGAG | 50717 |
rs7517599 | snp | A/C | 0.499824 | 0.00938333 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236263 | GAGGCATCACACACA[A/C]ACACACACACACATA | 50717 |
rs7538782 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232595 | ccagtggaccaagat[C/G]gtgccactgcactcc | 50717 |
rs9633341 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236604 | ACCTAGGTCTGCCTG[A/G]ATCCAAACAAGATGT | 50717 |
rs9660289 | snp | C/G | 0.45866 | 0.137698 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255806 | TATATTTTTAGTAGA[C/G]ACAGGGTTTTGCTAT | 50717 |
rs9661510 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260098 | TGCAAAAAAAAAAAa[A/C]caaaaaacaacattt | 50717 |
rs9662568 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260100 | CAAAAAAAAAAAACC[A/C]AAaaacaacattttt | 50717 |
rs10494338 | snp | C/T | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257181 | GTCACTACCCCATGC[C/T]TATTGCTGATTCAAT | 50717 |
rs10494339 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257478 | TAGTCACTTTATGAT[C/T]TTAAAAGCCTATTAC | 50717 |
rs10660397 | in-del | -/A/AA/AAA | 0.487621 | 0.0776941 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234242 | GTGAGACTGCACCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 50717 |
rs10732269 | snp | A/T | 0.439918 | 0.162576 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226932 | TCATATATCCGTGTG[A/T]AAGGTGGTAGTTAAA | 50717 |
rs10908770 | snp | C/G | 0.439363 | 0.163222 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219982 | GGACCAACCACCTCC[C/G]CTGCCTCACCTGCAC | 50717 |
rs10908771 | snp | C/G | 0.441977 | 0.16014 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246931 | ACCACTTCTCTCCAG[C/G]CAGGACGACAGAGCA | 50717 |
rs10908772 | snp | C/T | 0.441432 | 0.160792 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253288 | GGAGGATCGCTTGAG[C/T]CCAGGAATTTGAGAC | 50717 |
rs11265356 | snp | C/T | 0.148326 | 0.228391 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217103 | GACAGTTGGCTCCCC[C/T]CCCACCCCCAGCAAC | 50717 |
rs11265357 | snp | A/G | 0.0711525 | 0.174681 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217383 | TATGCACCTCTCCAT[A/G]GAGCCCCATTCCAGG | 50717 |
rs11265358 | snp | C/T | 0.147991 | 0.228242 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218128 | ACACATGGACGGCAA[C/T]GGACAAAAGTAGATA | 50717 |
rs11265359 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221639 | GTTCCCCACAGCTAA[A/G]AAGGAATAAAAAGGA | 50717 |
rs11265360 | snp | G/T | 0.148326 | 0.228391 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228746 | AGCTATTTCTCTATA[G/T]TCCCTTGAAGTAATT | 50717 |
rs11265361 | snp | C/T | 0.441841 | 0.160303 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242182 | CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA | 50717 |
rs11265362 | snp | C/T | 0.134802 | 0.221877 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242910 | CTCTAGAACCCTGTG[C/T]CTTTCAACTAAACCC | 50717 |
rs11265363 | snp | A/C | 0.459233 | 0.136827 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244618 | CCTATTATTATTATT[A/C]TTTCTTTTTTTTTTT | 50717 |
rs11265364 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247179 | AGCTGATGAGCTCAC[C/T]GTCCCAGGTAGTTGG | 50717 |
rs11265365 | snp | C/T | 0.161596 | 0.233848 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259305 | tttgggaggctgagg[C/T]gggcagatcacaagg | 50717 |
rs11284812 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256013 | CAGAACTAAGCAAAC[-/T]TTTTTTTTTTTTTTT | 50717 |
rs11375715 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258758 | CAAAAATAAAAAAAA[-/A]CTTTAGAAAGATAAA | 50717 |
rs11455653 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263490 | AAAAAAAAAAAAAAA[-/A]TTACCCGGCATGGTG | 50717 |
rs11591179 | snp | C/T | 0.444799 | 0.156695 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236277 | AAACACACACACACA[C/T]ACATACACGTACGTA | 50717 |
rs12071837 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248709 | tccatctcaaaaaaa[A/G]aaaaaaaaaaaaCTG | 50717 |
rs12075010 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258758 | CTATCTCTACAAAAA[A/T]AAAAAAAACTTTAGA | 50717 |
rs12082427 | snp | C/T | 0.161596 | 0.233848 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249007 | ggctggcctgaccaa[C/T]gtggtaaaaccccat | 50717 |
rs12091372 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226552 | TCCAATCTCAGAGCC[A/G]ATCTCTTGAAAAATG | 50717 |
rs12096571 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234931 | CCAAGCCTAAAACAT[G/T]TCTATCTTTTAAGCA | 50717 |
rs12128926 | snp | G/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263634 | tggaatgagactccg[G/T]ctcaaaaaaaaagta | 50717 |
rs12130998 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250406 | ggaaggcggaggttg[C/T]ggtgagccaagatcg | 50717 |
rs12145552 | snp | G/T | 0.00716713 | 0.0594884 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227392 | gcctcaacctgccgc[G/T]tagctgggactacag | 50717 |
rs12403037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226004 | acacaccaccacgcc[C/T]ggccaatttttgtat | 50717 |
rs12566097 | snp | C/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253377 | cacagtggctgacgt[C/T]taagtgacgctggta | 50717 |
rs12728099 | snp | A/G | 0.0141169 | 0.0828202 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230532 | TCACTATGGATAAAA[A/G]AAAGTGGTAGCTCAG | 50717 |
rs12730809 | snp | A/C | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256366 | GTACAACTTACAATA[A/C]AACATTAAAGAGAGG | 50717 |
rs12742133 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221186 | AAATGCTGGCCTGGG[A/G]GAGGGCATTCAGCCC | 50717 |
rs12746884 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221840 | aaaaaaaaaaaaaaa[A/G]GATAAGGTTAACCAG | 50717 |
rs12759667 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221187 | AATGCTGGCCTGGGA[A/G]AGGGCATTCAGCCCT | 50717 |
rs12760305 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160242205 | agccgagattgtgcc[A/C]ccgtactccagcttg | 50717 |
rs12760784 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221209 | TTCAGCCCTGCATCT[C/T]TCTGGAACAGAATGC | 50717 |
rs12760786 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221211 | CAGCCCTGCATCTCT[C/T]TGGAACAGAATGCAA | 50717 |
rs12760935 | snp | C/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221278 | CTTCTGACTTCCTTT[C/T]TCTAAATGCCTATTG | 50717 |
rs16831606 | snp | A/G | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216083 | GGACTTTCAGACTCA[A/G]TGACCAGTGATAAGA | 50717 |
rs16831610 | snp | A/T | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216260 | AGTTGGATGGCTTAA[A/T]GATCAAGCAGCTAAA | 50717 |
rs16831617 | snp | C/T | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216983 | TAATCAAGTGCAAAA[C/T]ACTGTGGTAAGTACA | 50717 |
rs16831619 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217011 | ACAGAGAATGAATAA[A/G]GTGGAAAGGAAAGTG | 50717 |
rs16831628 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223267 | AGGGCTCCACTCTCC[A/G]GAATCAGTAAAAGAA | 50717 |
rs16831632 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224136 | TAAAGAGGGCTTTCC[C/T]TGACTCCCTAACAAG | 50717 |
rs16831634 | snp | C/T | 0.0210248 | 0.100351 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224560 | GAGCTCTGCCAAGAA[C/T]AAGAACATAGCAGTG | 50717 |
rs16831635 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226232 | CCTACCGAAAAAGGT[C/T]ACTCACGGGCAGAAA | 50717 |
rs16831636 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226634 | AACCTCTTCCTCATC[A/C]CCAGCTGGCCACTTT | 50717 |
rs16831647 | snp | C/T | 0.247053 | 0.249983 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227162 | GAGCTGAAGACTGAG[C/T]TACTGGAGAACATCA | 50717 |
rs16831650 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230497 | AGTGTTAACAAAAGG[C/T]GTTCACGGTAACAAA | 50717 |
rs16831651 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230633 | CCAGTATTTAAAATT[C/T]CTAGTGCACGTTTAT | 50717 |
rs16831658 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234557 | GCACCAGATTCAATT[C/G]CTGGTGGCCTAACAG | 50717 |
rs16831661 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234893 | CTCTTGAAGGTTATA[C/T]AAACAAGCAACATAT | 50717 |
rs16831666 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238395 | GGCCAAATACTATGA[A/G]TGCATGATCTAGGGA | 50717 |
rs16831675 | snp | C/T | 0.0177783 | 0.092591 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160238682 | AGACAGTTCTGCTAC[C/T]CGAACCTGCCCGTCA | 50717 |
rs16831677 | snp | C/T | 0.021333 | 0.101051 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239483 | GCTGCATGCACCCTA[C/T]CTATGAGGCTTCCAA | 50717 |
rs16831680 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241348 | ATTTTTTAATATAAT[C/T]CTTAGTCACACATTT | 50717 |
rs16831691 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246482 | TTTGATTATGAACCT[A/G]TATGAGTGAAAACTT | 50717 |
rs16831694 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251913 | GTACTTGGAGGGGTC[C/G]AACATATGACACTGT | 50717 |
rs16831696 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255228 | ACGAACTGCAGTAAG[A/G]CAATCTACCCAGGAA | 50717 |
rs16831703 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257521 | ATACAAGACTTAGAG[C/T]ACGAAACTCAAGATC | 50717 |
rs16831708 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258934 | TCCTTTCCTTCACCC[A/G]ACATGGATCTTCAGA | 50717 |
rs16831709 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259832 | AATGAACAAAAAAAT[G/T]TACTGATGTTTAAGA | 50717 |
rs16831714 | snp | A/T | 0.0287284 | 0.116357 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264099 | AAAATTATGTTTGTG[A/T]TCCAGCTATACTACT | 50717 |
rs16831718 | snp | A/G | 0.123798 | 0.215808 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264107 | GTTTGTGATCCAGCT[A/G]TACTACTAGAATATA | 50717 |
rs28393438 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248710 | CCATCTCAAAAAAAG[A/G]AAAAAAAAAAACTGT | 50717 |
rs28434377 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160231965 | GGAGACTGAGGCGGG[G/T]GGGTCACTTGAGGCC | 50717 |
rs28537409 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160219743 | AGCTTAGGCAGCTTC[C/G]TTCTGTCCGAAAGGC | 50717 |
rs28620339 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160224703 | CAGGCAAGTCCGACT[C/G]TACAGGGTAGACTAA | 50717 |
rs28755822 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160222975 | CGCTCCTTAGGGCAG[A/G]GGAATCTGCAGTCCT | 50717 |
rs33929285 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260731 | AAAGAGCAGCCACTA[-/T]TTTTTTTTTTTTTTT | 50717 |
rs34003034 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220251 | CAATGCCTGGAATAG[C/T]ATCTATCTATAGTAA | 50717 |
rs34024988 | in-del | -/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160240849 | GACTTATGGATGTGG[-/G]TGTTGCACCATTTCC | 50717 |
rs34290129 | in-del | -/AA | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234257 | AAAAAAAAAAAAAAA[-/AA]TGCCTCTGACATAAG | 50717 |
rs34386233 | in-del | -/T | 0.478768 | 0.100824 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228092 | ATTTTTTTTTTTTTT[-/T]GGTAGAGACACAGTC | 50717 |
rs34387290 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221565 | TTGCAAAGAACCATT[C/T]TAAATTCTAAAACCA | 50717 |
rs34423588 | in-del | -/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253184 | AAATTAAACCTCTGG[-/G]AAGTCAAGAATAAAA | 50717 |
rs34468725 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260342 | AATCTCTAAAGACTG[G/T]ACTTTTCTCTTTATA | 50717 |
rs34602182 | in-del | -/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261625 | AATCTTTTCAACGCT[-/G]AAACCATAACCAAAC | 50717 |
rs34616491 | in-del | -/AG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249523 | TATACAAGAAAAAAG[-/AG]GCTCAGACCTGTTAT | 50717 |
rs34640035 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228106 | AATTTTTTTTTTTTT[-/T]GGTAGAGACACAGTC | 50717 |
rs34668985 | in-del | -/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160245419 | AGCCCTTTCATTCCC[-/C]ATGACAATTATTCCA | 50717 |
rs34763860 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160247950 | GTTAGGCAACAATTT[-/A]CTTAGGATAGGACAC | 50717 |
rs34800118 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258650 | ATTAGCTAGGTATGG[G/T]GATATGCCCCTGCGG | 50717 |
rs34995082 | in-del | -/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160262100 | GCTGGCTCTTGGGGG[-/G]CAACACCAGGGCTGA | 50717 |
rs35258380 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160243424 | TTTTTTTTTTTTTTT[-/T]AAAAAGACGGGGTCT | 50717 |
rs35549265 | in-del | -/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246405 | CACAGATGATAAAGG[-/G]TAAGTAGAATTAAAT | 50717 |
rs35765356 | snp | A/C | 0.0803491 | 0.183626 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260002 | TCAGTTGGGAAAATT[A/C]ACCAGAAAAATGTGT | 50717 |
rs35765703 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234193 | AAATGCCTCTGACAA[-/A]GATCATGCCACTGTA | 50717 |
rs35813537 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160222735 | CCACAGTCACTACCG[-/G]CTCACCACAAACTCA | 50717 |
rs35905532 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260833 | ACTCCCCAGCTTTTA[A/G]TCACAAGCAGCTAAA | 50717 |
rs35940301 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160231044 | AGGTGTGAGCCACTA[-/A]CACCTGACCATCATC | 50717 |
rs41265785 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261691 | AATCCCGGAGAGAAT[A/G]TGATAGCGCTAGTGC | 50717 |
rs55668179 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228893 | AGGAGAAACCTCAAA[A/T]CATTCAGTTGGCTGC | 50717 |
rs55749211 | snp | G/T | 0.0182805 | 0.0938406 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240389 | CATGTTAGTGAGGAA[G/T]GAGTAGAGGAGAGGG | 50717 |
rs55822344 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256157 | TGCACCTGGCTAAGA[A/G]AACTTTCTATAAAAA | 50717 |
rs56000332 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222837 | CATCAGGCCTATATA[C/T]ATTCATCTCAAAGGG | 50717 |
rs56056529 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228892 | AAGGAGAAACCTCAA[A/G]ACATTCAGTTGGCTG | 50717 |
rs56238993 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256155 | ACTGCACCTGGCTAA[A/G]AGAACTTTCTATAAA | 50717 |
rs56279945 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242599 | AAGCTCATCAAGAAG[G/T]CCCCAACAGTAAATC | 50717 |
rs56300764 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242014 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTAAG | 50717 |
rs56326104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227638 | CTTAAAGGACAAGAC[A/G]GTAAATGTTTTAAGC | 50717 |
rs56922661 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256512 | CCAGAGGAATACAGT[A/C]ACTTGACTACCATTA | 50717 |
rs57064431 | in-del | -/A | 0.147991 | 0.228242 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234816 | CAAAGCTAGTACTAG[-/A]AGGCAGAACCCTTGT | 50717 |
rs57097730 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237810 | CTCCCAAAGTATTGG[A/G]ATTACAGGCATAAGC | 50717 |
rs57658253 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229705 | ACTACAACCCTTTTT[-/G]ATCAACAGCTTCTTA | 50717 |
rs57978931 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246719 | AGGCACGGCAGCTCA[C/T]GCCTATAATCCCAGC | 50717 |
rs58090400 | in-del | -/A | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219763 | GTCCGAAAGGCACCC[-/A]ATGCCCCCTGCTGTC | 50717 |
rs58090894 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253472 | GGCCAACATGGTGAA[A/G]CCCTGTCTCTACTAA | 50717 |
rs58421777 | in-del | -/GTTTTT | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233066 | TTGGCTTTAGTTTTT[-/GTTTTT]AAGTCTAAGGTTTTA | 50717 |
rs58539770 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221840 | AAAAAAAAAAAAAAA[-/A]GATAAGGTTAACCAG | 50717 |
rs58635711 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248907 | CTCAAAAAAAAAAAA[-/A]GAGGGCGGGTGTGGT | 50717 |
rs58657104 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232484 | CGTCTCTACCAAAAA[A/T]AAAAAAATTAGCCGG | 50717 |
rs58736444 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262624 | GGCGGGGCTTAAGGC[C/T]AACGGAAAACAGAGC | 50717 |
rs58794144 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246960 | CAAGACACAGTCTCC[A/C]AAAAAATAAAAAATA | 50717 |
rs58903753 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255313 | TTTTTTTACTATTAT[C/T]ATCGTAGAGACGGAG | 50717 |
rs59002926 | in-del | -/AAAA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260094 | GATGTGCAAAAAAAA[-/AAAA]CCAAAAAACAACATT | 50717 |
rs59102401 | snp | A/G | 0.0433465 | 0.140692 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215848 | ACATTCCCTACCTCA[A/G]GGAGTAAGTACAGCA | 50717 |
rs59315993 | in-del | -/C/CAA/CAAA/CAAG | 0.00755907 | 0.0610114 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259550 | AAACAAACAAACAAA[-/C/CAA/CAAA/CAAG]AAAAACCTCTTCATT | 50717 |
rs59361846 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160247510 | GGCTGCTCTTTTCCT[C/T]TAATATGATGAAAGA | 50717 |
rs59567165 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254621 | ACATGGTAAAACCCC[A/G]TTTCTACTAAAAATA | 50717 |
rs59577067 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222913 | TAACAGATAGTTATA[A/G]GAATCACACCAGTCC | 50717 |
rs59684865 | in-del | -/TT/TTT | 0.487746 | 0.0773096 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228610 | CTTTTTTTTTTTTTT[-/TT/TTT]GGCCACAGGCCAAAA | 50717 |
rs59880776 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242142 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGAAGAA | 50717 |
rs60178749 | in-del | -/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236262 | GAGGCATCACACACA[-/C]AACACACACACACAT | 50717 |
rs60271354 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246155 | TCAAAAAAAAAAATT[A/T]AAAAAAACTTATAAA | 50717 |
rs60288000 | snp | C/T | 0.040671 | 0.13668 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264216 | TATTTAATGCCCCAC[C/T]GTCCTATTCATTCTT | 50717 |
rs60453098 | in-del | -/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236263 | AGGCATCACACACAA[-/C]ACACACACACACATA | 50717 |
rs60528208 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254898 | ATTCTACCTCTACCA[C/T]CTGCTTTTGAGTTTT | 50717 |
rs60860476 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256588 | GAAAAAGCCAGGAAG[-/A]AAAAAAAAAATGGCA | 50717 |
rs60934968 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248869 | ACTCACTGCACTCCA[A/G]TCTACGCAACAGAGT | 50717 |
rs60995786 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246301 | TCAAAAGCAGCTGCA[C/G]AGAACCTCTCTCAAA | 50717 |
rs61039791 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220753 | GAGATCTGGGCAAGG[C/T]AGAAAATAACTTCTA | 50717 |
rs61341479 | snp | A/G | 0.262159 | 0.249704 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236448 | TGTGTGTGTGTGTGT[A/G]TATATATATATATCC | 50717 |
rs61480108 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263153 | TATTTTTTTTTTTTT[-/T]CTTACCAGAAGCCCA | 50717 |
rs61489122 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255345 | CTCACTATCTTGCCG[A/C]GTGGTCTCAAACTCC | 50717 |
rs61510065 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256743 | TTTCATTAATAAGAT[A/G]ACATCTTTGTCATAT | 50717 |
rs61741888 | snp | A/C | 0.0570934 | 0.159019 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217675 | ACTCATCAGAGTCCG[A/C]GTCTGTGGCCCCAAC | 50717 |
rs61801277 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236499 | GGAAGGACGGAGGGA[A/G]GGAAAAAAATATGCC | 50717 |
rs61801278 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261983 | CGGTGGCCCTGAGGT[A/G]ACGGGGAGACGCAGG | 50717 |
rs67536616 | in-del | -/AAAC | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160259532 | GTCAAAAAACAAACA[-/AAAC]AACAAACAAAAAAAA | 50717 |
rs71574364 | in-del | GTG/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236261 | TGTGTGTGTGTGTGT[GTG/T]TGTGTGTGATGCCTC | 50717 |
rs71579664 | in-del | -/CA | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236280 | ACACACACACACACA[-/CA]TACACGTACGTATAT | 50717 |
rs71579665 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246382 | TAATTGCTCTAGAAA[-/A]TACATGTGCACAGAT | 50717 |
rs71628169 | snp | C/G/T | 3.33067e-05 | 0.00408072 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239749 | AGTACTGGCTGCCGC[C/G/T]GTACCCAATCCCACA | 50717 |
rs71628170 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160262233 | GGGGAAACCGGCTGG[A/G]AAGCGAGGGGGGGCG | 50717 |
rs71759232 | in-del | -/CAAA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160259547 | AACAAACAAACAAAC[-/CAAA]AAAAAAAACCTCTTC | 50717 |
rs71774677 | in-del | -/TGG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249055 | ATTAGCTGGGGGTGG[-/TGG]CACATGCCTGTAGTC | 50717 |
rs71811331 | in-del | -/A | 0.219349 | 0.248114 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257270 | CTGATAATCTGCTTT[-/A]AAAAAAAAAAAAGCT | 50717 |
rs72467723 | in-del | -/AAAA | 0.148661 | 0.22854 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260086 | GTATCAATGATGTGC[-/AAAA]AAAAAAAACCAAAAA | 50717 |
rs72706663 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226391 | CTCATTCTTATCAAG[C/T]ACACTACACCTTCAC | 50717 |
rs72706664 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242662 | TTCTGTAAAGGGCCA[A/G]ATAGTAAAAACCTTA | 50717 |
rs73027618 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231625 | GATTGGGGAAAAAAA[C/T]ATGTAGTGAAGTCAC | 50717 |
rs73027624 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236701 | ATACAAATGAACTGT[A/G]ATAAAACAGAACTCA | 50717 |
rs73027627 | snp | A/C | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238210 | TCCAGAAACAGTGCT[A/C]TTTGTGAACTGAGAG | 50717 |
rs74125505 | snp | A/G | 0.0277173 | 0.114413 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216907 | TCCCACCTCTTCCCA[A/G]CCTCCCTCACCTGAC | 50717 |
rs74125506 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217109 | GGGGGTGGGGGGGGA[A/G]CCAACTGTCATAAAC | 50717 |
rs74125507 | snp | C/T | 0.00905257 | 0.0666659 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218828 | GCAGAAAGAAAATAA[C/T]TTCTGCAGTCAGCCA | 50717 |
rs74125508 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219618 | AGCTATAAGGCAGCA[C/T]ATTAAAACCAAGCAG | 50717 |
rs74125511 | snp | A/G | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220854 | ACTGCTGAGTCTACT[A/G]CATTGAAAGTAGTGC | 50717 |
rs74125513 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224260 | TGGCAAGAGATGCTC[C/T]TGAGCGCTTTCTCCT | 50717 |
rs74125514 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224371 | TTTCTATTTGTATAA[C/T]CTGAGTAAGACACTG | 50717 |
rs74125515 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225399 | TATTTCTATTTTGTC[A/G]ATTAAAAAACTGAGG | 50717 |
rs74125516 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228743 | GTAAGCTATTTCTCT[A/G]TATTCCCTTGAAGTA | 50717 |
rs74125517 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231562 | TCTGTTTGTTTTGTA[C/T]GTAACAACAGGAAAA | 50717 |
rs74125519 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233479 | CTAATGGTGTCCCCC[A/G]CACATCTCAAAAACA | 50717 |
rs74125521 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233850 | TGAACTCTGCAGGGG[A/G]CATGCAGAGGTGCTA | 50717 |
rs74125522 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234464 | GATTCATGGTTAACT[C/T]TCAGCCAGACTTTCT | 50717 |
rs74125524 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238102 | TGGCACAAAAGACCA[A/C]CACCATGCCTACCTT | 50717 |
rs74125527 | snp | A/G | 0.0193831 | 0.0965186 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239571 | ATTAGGGGAGCCAAA[A/G]TAGGGCCATGTCCCG | 50717 |
rs74125530 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241548 | TGCATTCTCTTAACT[C/T]ACAACAGTCAAGTCA | 50717 |
rs74125532 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243046 | TCCAATCACATCAAC[C/T]AGAATTTAGCCTGTT | 50717 |
rs74125533 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244526 | TTCTGAGTATCATTT[C/T]ACACACAAATCAACA | 50717 |
rs74125534 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247422 | ACTAAAAACCAGGCA[A/G]AAAGACTTTACTACG | 50717 |
rs74125535 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252218 | GGCAGTCACAATCCC[A/C]TTTGTAGCCAATTAA | 50717 |
rs74125544 | snp | C/T | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255350 | TATCTTGCCGCGTGG[C/T]CTCAAACTCCTGAGC | 50717 |
rs74125545 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257077 | GTTTCTTGGCTACAT[C/T]TGTAAAAATAAAAGA | 50717 |
rs74125547 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257314 | AGACTTAAAAACTAA[A/C]TCTAACACCAATGTT | 50717 |
rs74125549 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259262 | CTCTTTGGCCGGGCA[C/T]GGTGGTTCACACCTG | 50717 |
rs74125550 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260752 | AAATTTCCCACTATA[C/T]CCTAAAAAGTCGGAA | 50717 |
rs74125551 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260921 | TGATTTGACAACAGG[A/C]TGAACAGAACTCAGG | 50717 |
rs74318373 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226639 | CTTCCTCATCACCAG[C/T]TGGCCACTTTCTAAA | 50717 |
rs74327467 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219987 | AACCACCTCCGCTGC[C/T]TCACCTGCACAGGCA | 50717 |
rs74368137 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264218 | TTTAATGCCCCACCG[G/T]CCTATTCATTCTTTC | 50717 |
rs74388939 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227575 | GTGTTTATTAATAGC[C/T]TACTATATTCTACAT | 50717 |
rs74407559 | snp | A/C | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260086 | GTATCAATGATGTGC[A/C]AAAAAAAAAAACCAA | 50717 |
rs74496850 | snp | G/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235154 | TTGGTTTTTTTTTTT[G/T]AGACAGTCTTGCTGT | 50717 |
rs74585485 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261809 | CCGTTCTAAGATATC[C/G]TAAAAGATTTGGGAG | 50717 |
rs74597280 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227230 | ACAACACTGAGGAGT[C/G]GTTGGACATCAAGGA | 50717 |
rs74626067 | snp | A/G | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249116 | AATCGCTTGAACCTA[A/G]AAGGCAGAGGTTGCA | 50717 |
rs74816858 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251667 | GATGGTGGTGGGGAA[C/T]ATGTTGCCCAGGCTG | 50717 |
rs74940958 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252345 | TATATTTAGTTTCAG[A/G]GAAAAACGAAATGCT | 50717 |
rs74976204 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261424 | AATAAAAATATTTAT[A/G]AATACACTTTAGTAT | 50717 |
rs75011122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223457 | ACAAAATCATGACAG[A/G]TATCTGCTAGGAGTG | 50717 |
rs75042431 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236484 | GAAACTACTAGAGAG[A/G]GAAGGACGGAGGGAG | 50717 |
rs75118560 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257759 | CTCTGTTGCCCATAC[G/T]AAACTGCAGAGGCGC | 50717 |
rs75184724 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234612 | CAGGATAAGATCTCA[C/T]TCTGTTTCACAACTC | 50717 |
rs75343243 | snp | C/T | 0.125948 | 0.217051 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236331 | GTGTGTATATAAATA[C/T]ATATGTGTGTATATG | 50717 |
rs75426089 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228411 | GAAGAGATGATTTAC[C/T]GACTGTGCTTCATCA | 50717 |
rs75472328 | snp | A/C | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232207 | AGAGCAAGACTGTCT[A/C]AAAAAAAAAAAAGTC | 50717 |
rs75502519 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236420 | TATGTGTGTGTATAT[A/G]TGTGTGTGTGTATGT | 50717 |
rs75584156 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243043 | TCCTCCAATCACATC[A/G]ACTAGAATTTAGCCT | 50717 |
rs75745563 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260587 | AACCTGAAAGCCTCA[C/T]GAAAACTGCATTTAT | 50717 |
rs75819532 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259864 | TACATTTTGAAATAT[A/T]CATACACCAATATCT | 50717 |
rs76152438 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217895 | TCAACTCATTGTAGC[A/G]TGAAGGCCGCCACAG | 50717 |
rs76177337 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236474 | TATCCTCACAGAAAC[C/T]ACTAGAGAGGGAAGG | 50717 |
rs76213215 | snp | A/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244065 | GAAGAAACCAAAACA[A/T]TTAGGAAACCACCTG | 50717 |
rs76261303 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226385 | CCTTTCCTCATTCTT[A/T]TCAAGCACACTACAC | 50717 |
rs76356320 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245451 | AAGCAGCCTCATCCT[C/T]ATCTTTTCCTCCGCT | 50717 |
rs76358355 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217808 | TAGGCCAGAGATCAG[C/T]AGAATTTTTCTTAAA | 50717 |
rs76464728 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236394 | TGTGTGTATATATGT[A/G]TACATGTGTATATGT | 50717 |
rs76486295 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261423 | TAATAAAAATATTTA[A/T]GAATACACTTTAGTA | 50717 |
rs76559273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254515 | GGTTTTTTTTTTGGC[C/T]AGGTACCATGGCTCA | 50717 |
rs76573195 | snp | C/G | 0.0275645 | 0.114116 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217533 | GCCTGGGACAGGAAA[C/G]GGTTGCCCAGGCAGG | 50717 |
rs76596795 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238225 | ATTTGTGAACTGAGA[A/G]TTTGAGCAGGTAAGC | 50717 |
rs76649185 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228078 | ATTAATTAAAAAATT[A/G]AAATTTTTTCTTAAT | 50717 |
rs76649657 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248402 | CTACAAAACATGTAT[C/T]TGATCAAGGACAGTA | 50717 |
rs76716742 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234656 | ATTAAATAAACTTAC[C/T]ATCATTTTTTCCTTT | 50717 |
rs76717618 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242207 | CCGAGATTGTGCCAC[C/T]GTACTCCAGCTTGGT | 50717 |
rs77035081 | snp | A/G | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257593 | TACTAGAATCTGTTT[A/G]CTTTTAAAATGCCAG | 50717 |
rs77073091 | snp | C/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222568 | TATCATGTAGTCACA[C/G]TGAGAATTCAGTGTC | 50717 |
rs77216851 | snp | A/G | 0.029116 | 0.117091 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252203 | TACAAATATAAACAA[A/G]GCAGTCACAATCCCA | 50717 |
rs77252982 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237367 | TTTTGTCATAAAATC[C/T]CAGGAAAGGACATAA | 50717 |
rs77364457 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254437 | GAATAATTTATATAC[A/C]TATGTTTATAAGAAA | 50717 |
rs77447084 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234597 | TCTGAACCTGATCCA[A/C/T]AGGATAAGATCTCAC | 50717 |
rs77474884 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227338 | AGTTAGGTTACTGAT[A/G]ACTTAAGCCTTGACA | 50717 |
rs77552362 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253445 | GGCCAGACTGGTCTC[A/G]AACTCCTGGCCTCAA | 50717 |
rs77580904 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229698 | TATACAAACTACAAC[C/G]CTTTTTGATCAACAG | 50717 |
rs77605661 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160247441 | GACTTTACTACGCTG[C/G]ATAAGAGTACTCTGT | 50717 |
rs77677179 | snp | A/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230528 | GATATCACTATGGAT[A/T]AAAAAAAGTGGTAGC | 50717 |
rs77791113 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225391 | GTTATTTTTATTTCT[A/G]TTTTGTCGATTAAAA | 50717 |
rs77827302 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240884 | TTAAGAAAGTATCAG[A/G]CCAGGCACGGTGGCT | 50717 |
rs77828128 | snp | C/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238517 | ATGACCACAACAAAT[C/G]TGACACAATGGGCAG | 50717 |
rs77862474 | snp | A/C/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242583 | GGCCAGAGGGTATCA[A/C/G]AAGCTCATCAAGAAG | 50717 |
rs77921780 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232608 | ATCGTGCCACTGCAC[A/T]CCAGCCTGGGTGGCA | 50717 |
rs77962469 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228836 | TTTCAAATTTATACC[A/C]GAAGATGAGCTGTTT | 50717 |
rs77987023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238878 | AACTTAGCTTTCCTA[A/C]TCTTGTACAGCTGGC | 50717 |
rs78160541 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250008 | AATGAAACTGACTAC[A/G]AAAGGGCATGAGAAA | 50717 |
rs78205822 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237711 | TTTTCGCTTTTTTTT[G/T]GTTTGTTTTCCACAG | 50717 |
rs78214153 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243295 | GAGGAGGGAAAGGAA[C/G]GAAGGAAGGAAATAA | 50717 |
rs78215158 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228204 | AGTGCTCTAGTTTTA[C/T]AGTCATGAGCCACCA | 50717 |
rs78277274 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222251 | TATCTGCTAATCTAA[C/G]ATCCAGCCAAGATCA | 50717 |
rs78317934 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259510 | AGCACCCCAGCCTGG[C/T]GACAGAGCAAGACTC | 50717 |
rs78462104 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221789 | CTTGTAACAGAAAGC[A/G]ATTGAACTCCTTCCT | 50717 |
rs78526052 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231614 | GGGACTTTGGGGATT[A/G]GGGAAAAAAATATGT | 50717 |
rs78571980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245512 | AAAAGTATCCTCTGT[A/C]AAAAGACAGTAGCCC | 50717 |
rs78595702 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247660 | AAAATTCAAAATCCA[A/G]AATGCTCCAACGAGT | 50717 |
rs78638705 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240808 | TTCTTAGCGAAAGAC[A/G]GAAACCAGCTGATAA | 50717 |
rs78719483 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235777 | GGAGTTTTGCTCCGT[C/T]ACTCAGGATGGAGTG | 50717 |
rs78724201 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219425 | TGAACCCCCAGAGAA[A/G]AGTCGGAGAACTATA | 50717 |
rs78822508 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257347 | GCAATAAAAAGTCTG[C/G]TTTGGATACCGTTAT | 50717 |
rs78842686 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230658 | GTTTATTTACATACG[A/G]AAAAGGTAGATTATT | 50717 |
rs79003004 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251512 | CAGGGTCTCGCTGTT[G/T]TCCAGGCTGGAATTC | 50717 |
rs79040838 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241760 | CCAGTATGAGCTATT[C/G]AACTCCAATACCACA | 50717 |
rs79079199 | snp | C/G | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221583 | AATTCTAAAACCACT[C/G]TCTGAAAAAACCTCA | 50717 |
rs79165634 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258619 | AAACAAACAAACAAA[A/C]AAAAAACAACCAAAA | 50717 |
rs79281090 | snp | A/G | 0.00028762 | 0.0119886 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225705 | TAAAAATGTACAAAC[A/G]AAACCCTTGAAGAGC | 50717 |
rs79420381 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160254516 | GTTTTTTTTTTGGCC[A/T]GGTACCATGGCTCAC | 50717 |
rs79628794 | snp | A/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230527 | AGATATCACTATGGA[A/T]AAAAAAAAGTGGTAG | 50717 |
rs79667478 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251551 | GATCTCAGCTCACTG[A/C]AGCCTCGATCTCCCA | 50717 |
rs79684147 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234241 | GAGTGAGACTGCACC[A/T]CAAAAAAAAAAAAAA | 50717 |
rs79709775 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249650 | AATAAATAAGATAAA[C/T]AAGAAGGAAAATGTA | 50717 |
rs79870736 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247794 | TGAACATTCAACTGC[C/T]AAAAGAAAAAAACTA | 50717 |
rs79897543 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228052 | CATACCACCACACCT[A/G]GAGATATTTAATTAA | 50717 |
rs79921865 | snp | A/C | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232208 | GAGCAAGACTGTCTC[A/C]AAAAAAAAAAAGTCA | 50717 |
rs80142865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226833 | GACTTCTCTGGCTGA[A/C]GTCATCAGTTAATTA | 50717 |
rs80196308 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160254513 | CTGGTTTTTTTTTTG[A/G]CCAGGTACCATGGCT | 50717 |
rs111397883 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219177 | ACCAGGCACATCAAT[C/T]ATTTCCTATGTATAG | 50717 |
rs111419858 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240903 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 50717 |
rs111485310 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240930 | AGCACTTTGGGAGGC[C/T]GAGGCACGTGGATCA | 50717 |
rs111582764 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242136 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 50717 |
rs111606935 | in-del | -/T | 0.159622 | 0.233092 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254501 | TTTGAAAAGCCCTGG[-/T]TTTTTTTTTTGGCCA | 50717 |
rs111703274 | snp | A/C/G | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254839 | GACAGCATGTGTTAT[A/C/G]AAAGAAAGAAAAGGG | 50717 |
rs111774998 | snp | C/T | 0.0513262 | 0.151752 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263511 | CGGCATGGTGGAGCG[C/T]GCCTGCAATCCCAGC | 50717 |
rs111880588 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252618 | ATTTTGTCAAAGATA[A/G]TAAGATGGACTGAAA | 50717 |
rs111958303 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218105 | TTTGCCTTTATGAAG[A/G]TAGCATTACACATGG | 50717 |
rs112012061 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222797 | CTGAAATGATAAATG[A/G]GGGAAGAAACCACAT | 50717 |
rs112054442 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242262 | AAAAAAAAAAAAAAG[C/T]CTCAACTAAGAGCAC | 50717 |
rs112113069 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256016 | AACTAAGCAAACTTT[A/T]TTTTTTTTTTTTTTT | 50717 |
rs112223146 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245960 | CCTGAGCAACATGGA[A/G]AAACCCTGTCTCTAC | 50717 |
rs112303310 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246899 | TAGAAGTTGAGGCTG[C/T]AGTGACCTGTGATTA | 50717 |
rs112327682 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245540 | CCCAAAGATTGTTCA[C/T]AATAGGCCAAGGTGG | 50717 |
rs112373015 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252463 | GAGCAAGAAAAGATA[G/T]GGAGGTTAAAAACCT | 50717 |
rs112681266 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250454 | CTGGGCAACAAGAGC[A/G]AAACTGTCTCAAAAA | 50717 |
rs112770628 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256025 | AACTTTTTTTTTTTT[A/T]TTTTTTTTTTTTTTT | 50717 |
rs112878524 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246756 | GGAGGCCGAGGCAGG[A/G]GTTGGAGACCAGCCT | 50717 |
rs113023280 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258616 | AAAAAACAAACAAAC[-/A]AAAAAAAAACAACCA | 50717 |
rs113069462 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160231046 | GGTGTGAGCCACTAC[A/C]CCTGACCATCATCTA | 50717 |
rs113143073 | snp | A/C/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215373 | TTGATTGTATTGCAA[A/C/G]TAACTGATTTTAAAA | 50717 |
rs113168576 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237813 | CCAAAGTATTGGGAT[C/T]ACAGGCATAAGCCAC | 50717 |
rs113326447 | in-del | -/GCTACCAGAAACCTGAAAGCCTCAC | 0.0513262 | 0.151752 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260563 | GAGCCTCTAGTCTCT[-/GCTACCAGAAACCTGAAAGCCTCAC]GAAAACTGCATTTAT | 50717 |
rs113385596 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236491 | CTAGAGAGGGAAGGA[C/T]GGAGGGAGGGAAAAA | 50717 |
rs113494190 | snp | C/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220572 | AATAATGCCTGAGCA[C/G]AGAAAAGAGCTCTGG | 50717 |
rs113595718 | snp | C/G | | | splice-donor-variant | DCAF8 | GRCh38.p7 | 1:160218323 | TCCAACCCTAGCTTA[C/G]CCGGTGATGGCGTCT | 50717 |
rs113602393 | snp | C/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237084 | AAGACATATGGAATA[C/T]GTTCAAGGCTAAGAG | 50717 |
rs113830535 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243357 | AAATAAGGAGGGGAA[A/G]GATGTCCCACTCCTA | 50717 |
rs113990572 | snp | A/C | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259531 | AGCAAGACTCGTCAA[A/C]AAACAAACAAACAAA | 50717 |
rs114094858 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222100 | ACATTTCACCCCTAA[A/T]TACTTCAACATGTAT | 50717 |
rs114226599 | snp | C/G/T | 0.0170316 | 0.0907494 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253508 | CAAAAATTAGCCACA[C/G/T]GCGGTGGCATACGCC | 50717 |
rs114265978 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240791 | GAGCTAGCATAGCCA[C/T]CTTCTTAGCGAAAGA | 50717 |
rs114332728 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234995 | TTTCTGGACTTAGCT[C/T]TCCAAAAATAAGTCT | 50717 |
rs114590076 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243114 | GTGCTGCCCAACTAT[A/T]TCCATTTAAAGGCGG | 50717 |
rs114671371 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245156 | CCAGCTTTCACCAGA[C/T]TCATCTTTCCTTAAC | 50717 |
rs114777785 | snp | C/G/T | 0.0034412 | 0.0413376 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239654 | CAGATTTCTCTAACT[C/G/T]ATGCCTGATTCTCTC | 50717 |
rs114946237 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230432 | TTAACTAATACATAT[A/G]GAGACTGAATCCACA | 50717 |
rs115059279 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221864 | TAACCAGATACATCT[G/T]AAGAGCTGATTGCTC | 50717 |
rs115260904 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262902 | CTTTGTTTCCTTAAG[C/T]GGTTTCTATACTATC | 50717 |
rs115325783 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245274 | ATTCCAAAGAGCAAA[G/T]AATAATATTATTCAG | 50717 |
rs115358206 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245525 | GTCAAAAGACAGTAG[C/T]CCAAAGATTGTTCAT | 50717 |
rs115398327 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257066 | ACAGCAATGATGTTT[A/C]TTGGCTACATTTGTA | 50717 |
rs115798383 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256267 | TACATCAGAAGTCTG[A/T]TGCCATTAACAGTTT | 50717 |
rs115876279 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247144 | ATCTAGTCCAAAGCT[A/G]ATCTTGCTGAGGTTG | 50717 |
rs116232064 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233648 | GCAATTTGAAATTTC[A/C]GAAGGACAAGGTCAA | 50717 |
rs116368954 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221459 | CCTAGATCTATGCAG[A/G]TCCCAGGTCCCTGAA | 50717 |
rs116384115 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238913 | CCCAATTTCTTCCAG[C/G]AGTTAAAGGAAAGGG | 50717 |
rs116470403 | snp | A/C | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228157 | GCCTTGAACTTCTGA[A/C]CTCAAGCTATCCTCC | 50717 |
rs116714301 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261866 | TATTACAAAGGGTAC[A/C]AGACCACAAGACAAC | 50717 |
rs116743190 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252538 | GGTAAGGTATAGTTG[A/T]TTAGTTAAGAAGTAT | 50717 |
rs116777323 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247766 | TGGGATGCTCAACTT[C/G]TACCAGAATAACTGA | 50717 |
rs116934049 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252540 | TAAGGTATAGTTGAT[C/T]AGTTAAGAAGTATAA | 50717 |
rs117207110 | snp | A/G | 0.089084 | 0.191327 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243449 | GGGTCTCGCTATGTT[A/G]CCCAGGCTGGTCTCA | 50717 |
rs117342925 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246412 | TGATAAAAGTAAGTA[A/G]AATTAAATGTCAAAA | 50717 |
rs117463128 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257773 | CTAAACTGCAGAGGC[A/G]CAATCTCAGCGCACT | 50717 |
rs118014330 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215722 | CACAGAGCAGCAGTC[A/G]GGAGAAGAAAAGCTT | 50717 |
rs137879012 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227294 | AAGAGTAGAGAAAAA[G/T]ACTTGAAAAGTACTT | 50717 |
rs137916237 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218390 | ACTATCAAACAGGTC[A/G]GTTTGGTGCAAGCTA | 50717 |
rs137988785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261448 | TTAGTATTTTTAGGC[C/T]TTCTCAAAACTACTT | 50717 |
rs138177087 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241130 | GCACTCTAGCCTGGG[C/T]GACAAAGCGAGACTC | 50717 |
rs138208121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246575 | TGAGAAAGGACTGCT[C/T]GAGCTCAGGAATTCA | 50717 |
rs138208738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237513 | ATAGCAAAGAAAAAC[A/G]TCAGCCATTAGAGTT | 50717 |
rs138325327 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250083 | TGTTACATAACTATG[A/C]CTTTGTCAGAATTAA | 50717 |
rs138332814 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256573 | GCTAAGAAAAAGCCA[A/G]GAAGAAAAAAAAAAA | 50717 |
rs138465222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221515 | TGAAATACCCTTTCA[C/T]CAGGGCAAGAAAAAC | 50717 |
rs138523324 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259612 | AAAAGAGACCTTTTC[C/T]TCATACAGTTCTTTG | 50717 |
rs138778532 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246035 | CCCAGCTACTAGGGA[C/G]GGTGAGGCAGGGGAA | 50717 |
rs138812017 | in-del | -/T | 0.0189856 | 0.0955633 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215298 | CTGTGAGATTGCCCC[-/T]ATCTTGTGCTCTTCT | 50717 |
rs139058905 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254288 | GATTGTGCCACTGCA[C/T]TCCAACCTGGGCCAA | 50717 |
rs139235747 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260200 | CCTGGGAGGTAAGTG[A/G]TATTATCACACTTTT | 50717 |
rs139254842 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262976 | AGAAGGGGCTCAGTA[G/T]CTTGAGGTGTAGCTA | 50717 |
rs139274225 | snp | C/G/T | 0.00874735 | 0.0655527 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257558 | TTTCACAACAGGGTG[C/G/T]GCTTCTATACAATGT | 50717 |
rs139316396 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220194 | ATATCAGCCTATTGT[G/T]AAGTTTATCTTTGGG | 50717 |
rs139426438 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216322 | GTATGTGTGTGGTGT[C/G]TGTGTACATGTCTTC | 50717 |
rs139547966 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160242680 | AGTAAAAACCTTAGG[A/C]TTTGCAGACCATACG | 50717 |
rs139627011 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228466 | AGCAATAAATTTTCA[C/T]GTCAGCCAAATTTAC | 50717 |
rs139657718 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233325 | AGACTGAGGTGGGAG[A/G]ATCGTTTGAATCCAG | 50717 |
rs139690630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238448 | AGGAGTTTAGGGTGG[C/T]TGCTTTTGCTCCTTT | 50717 |
rs139768121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239311 | TAACCCTATGTGTTA[C/T]TAGTCCCATTTTACA | 50717 |
rs139818841 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230049 | TCTATGGCTACACAT[A/T]TAAGGACTGTTGGTG | 50717 |
rs139829744 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261750 | ATCATGAGTCAGAAA[C/T]TCAAGCCACCAGATG | 50717 |
rs139882151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243283 | CCTGAAAAGAAGGAG[A/G]AGGGAAAGGAAGGAA | 50717 |
rs139981832 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258668 | TATGCCCCTGCGGTC[C/T]CAGCTACTCAGCTGA | 50717 |
rs139994575 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234239 | AAGAGTGAGACTGCA[C/T]CTCAAAAAAAAAAAA | 50717 |
rs140248185 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248183 | GTGGTGGCACATGCC[C/G]GTAGTCCCTGCTACT | 50717 |
rs140255971 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245908 | CTTTGGGAGGCCGAG[C/G]AGGGCAGATCACCTG | 50717 |
rs140362219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259140 | GTACTTAATTTTCAT[A/G]TGCCCTTGCCAAAAA | 50717 |
rs140418367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253986 | TTTTCTCTCCAGTAA[A/G]GAATCATAAAACACT | 50717 |
rs140428690 | in-del | -/A | | | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263139 | CTGCCAGGCTGGGGT[-/A]TTTTTTTTTTTTTTC | 50717 |
rs140470365 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256107 | GTCCTCCCAACTCAG[C/G]CCCCCGAGTAGTTGG | 50717 |
rs140639578 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236366 | TACATATGTGTGTAT[A/T]TAAACATATATGTGT | 50717 |
rs140685497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231204 | GTTAATGGATTCCTA[C/T]AAAATTCGTAACTCT | 50717 |
rs140852727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249243 | TTGAAAAGATCCTCA[A/G]CATTATTAATAATTA | 50717 |
rs141000337 | snp | C/G | 0.000115339 | 0.00759318 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160224503 | CCCATCACTGTGAGA[C/G]GAGTTGAAGAGGTAA | 50717 |
rs141055794 | snp | A/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240027 | TAGGGCCCGCTCATC[A/T]TCTGATGAGTCCTGG | 50717 |
rs141233812 | snp | A/G | 1.64776e-05 | 0.00287028 | DCAF8 | 1 | allele_origin=G(germline)/A(somatic) | 1:160239870 | GCCCATGCTGCAGGC[A/G]GAAACGCTGCACAAA | 50717 |
rs141369018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240527 | GAGTACCCTCTGAGG[A/G]GAAATCTTGTAAAGG | 50717 |
rs141525896 | in-del | -/TA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236447 | ATGTGTGTGTGTGTG[-/TA]TATATATATATATCC | 50717 |
rs141612233 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226879 | TAGGTGTAAGTCTAG[A/C]GTTCAGAATAAGTGT | 50717 |
rs141703364 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237535 | CATTTTCTTTTTTTT[-/T]CCAGTCAGGGTCTCA | 50717 |
rs141839844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261783 | TTCCAACTAACAGGG[A/C]CCAAATGGGACCGTT | 50717 |
rs141883523 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238089 | CAACCTCTTTTCATG[G/T]CACAAAAGACCAACA | 50717 |
rs141883779 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220318 | CTATCTCCTAATAAG[C/T]CCTTGTTACAGACCT | 50717 |
rs141970245 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221002 | TCAGGGGTAGCCTCT[A/G]TATCTCTTATTCTAC | 50717 |
rs142000064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245210 | CTTCCTTTTATGCCA[C/T]TATAAAACATTCATA | 50717 |
rs142007100 | snp | C/T | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218325 | CAACCCTAGCTTACC[C/T]GGTGATGGCGTCTCT | 50717 |
rs142061277 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215310 | CCCTATCTTGTGCTC[G/T]TCTGTCTGCAGTGTG | 50717 |
rs142110509 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240706 | ATTGGCTCTGTTGTA[C/T]TGGATGGGCATTTAT | 50717 |
rs142168388 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223883 | CCATAATTGCACCAT[G/T]GCACTCCAGCCTGGA | 50717 |
rs142249687 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241515 | CTTTTATCGATCTTA[C/T]CTCCTATAACTACAT | 50717 |
rs142311348 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232227 | AAAAAAAAGTCACTT[A/G]AAACCCAACTTAAGC | 50717 |
rs142352428 | snp | A/G | 9.88582e-05 | 0.00702989 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160224518 | GGAGTTGAAGAGGTA[A/G]ATGTCTTCATCATTG | 50717 |
rs142402128 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227389 | CCCGCCTCAACCTGC[C/T]GCGTAGCTGGGACTA | 50717 |
rs142451806 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236028 | ACAGGCGTGAGCCAC[C/T]GTGCCCTGCCCACAA | 50717 |
rs142513538 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258603 | CCTCATCTCTTTAAA[A/C]AAACAAACAAACAAA | 50717 |
rs142577308 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244780 | CTGCCACCATGCCCA[C/G]CTTTCTGTATTTTTA | 50717 |
rs142618025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259617 | AGACCTTTTCCTCAT[A/G]CAGTTCTTTGATAAT | 50717 |
rs142621548 | snp | G/T | 0.00019181 | 0.00979122 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263240 | TCATTACATATTACT[G/T]AAGACTACCGCAATA | 50717 |
rs142684645 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160222710 | ATGATTTCTCCCAGA[A/G]GAAGATGTGCCCACA | 50717 |
rs142725744 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250193 | ATGCAGGCCGGCGCA[C/G]TGGCTCATGCCTGTA | 50717 |
rs142744523 | in-del | -/C | 0.0134861 | 0.0810011 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225513 | TCCAAGCTCTTCCCA[-/C]CCATACCAACAAGTT | 50717 |
rs142744762 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257936 | AGGTCTCAATATTGC[C/T]TAGGCTGGACTTGAA | 50717 |
rs142816267 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247153 | AAAGCTAATCTTGCT[A/G]AGGTTGGAAAAGCTG | 50717 |
rs143037091 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232413 | TTTGGGAAGCCGAGG[C/T]GGGTGGATCATGAGG | 50717 |
rs143046842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243003 | TGGAGCAATAAAAAA[G/T]CATGTTGAAAATCTC | 50717 |
rs143263508 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260668 | AGGATGTTTCTTCTG[A/C]TAACCAAGAATTCTT | 50717 |
rs143349563 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226585 | TTTCATTTCATCCTT[C/T]CAGGGACCTTGTTTG | 50717 |
rs143391219 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254655 | AAATTAGCTGGGCAT[G/T]GTGGCATGCGCCTGT | 50717 |
rs143395129 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160237206 | AGATAAGAACGTACA[C/G]GGAGAGTCTGGTTCC | 50717 |
rs143510230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258846 | GATGTCACCTGGACA[C/T]TCTTACCCAGCACAT | 50717 |
rs143577369 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237048 | AGGTACTATTCGGAT[C/G]AACCAGAGTTAGGCA | 50717 |
rs143618596 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248832 | CTAGGAGTTCAAGGC[C/T]GCAGTGAGCTATGAT | 50717 |
rs143664509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259526 | GACAGAGCAAGACTC[A/G]TCAAAAAACAAACAA | 50717 |
rs143859155 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261585 | CAGCTCCACTAAAAC[C/G]TAAAGTCATTTAAAA | 50717 |
rs143956585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256715 | CCAATCCACTAGACA[C/T]ACTATTAATACATTT | 50717 |
rs143994434 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252359 | GGGAAAAACGAAATG[C/T]TTCCATGGAAAATTA | 50717 |
rs144140924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222490 | GAAGAAAATACTCCA[C/T]CAAAAACTCAGCACC | 50717 |
rs144158120 | snp | A/G | 0.000365892 | 0.0135208 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239778 | CACCACCACCTTCAG[A/G]TCATCGCTGCCACTG | 50717 |
rs144211913 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248658 | CAGTGAGCTGCGATC[A/G]CGCCACTGCACTCCA | 50717 |
rs144374957 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239386 | AGCTAGTAAGCAGAA[G/T]GGCTAGGATTTGAAC | 50717 |
rs144537625 | snp | C/T | 0.000395342 | 0.014054 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160222683 | CCTCCATGAACTGAA[C/T]AATCTGGCAGGATGA | 50717 |
rs144560832 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229373 | AGGCTGATAAGACAC[A/T]GAAGATTTGAGTATT | 50717 |
rs144582549 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160225072 | CGTACCTGTGCCGTC[A/G]TGGCTGTACACAAGA | 50717 |
rs144592310 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224794 | GAATGAGTCAAAGGC[A/G]TAAGAACCTGCTCAG | 50717 |
rs144631187 | snp | C/G | | | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240095 | GCTGCTCTTCTTCCT[C/G]CTCTTCTTCCTCCTC | 50717 |
rs144644529 | snp | A/G | 0.0027826 | 0.0371962 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239808 | GGCCAGCCAGGTGCC[A/G]CGCTGGTTAAAGTGC | 50717 |
rs144707637 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229893 | CCAGGCGTGGTGGCG[C/T]GCACCTGTAATCCCA | 50717 |
rs144860940 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250783 | TGATAACTAAGAATA[C/G]CAGAAATTTAAGTAG | 50717 |
rs145008092 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250315 | TTAAAAGTACAAAAA[A/T]ATTAGCCGGGCGTGG | 50717 |
rs145121371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247942 | TGACCTTGGGTTAGG[C/G]AACAATTTCTTAGGA | 50717 |
rs145143292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254478 | TACCTTTCAGCTTCA[A/T]CTCTTGGCTTTGAAA | 50717 |
rs145334587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234675 | ATTTTTTCCTTTTTT[A/G]CTCTTCCCTATGAAA | 50717 |
rs145339170 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160231371 | GATCGTATACAGCCC[C/G]ACTTTCTTCTCTTTC | 50717 |
rs145344286 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160231316 | CAAACTGATCTCGTC[C/T]ACCCACTGCAAACTG | 50717 |
rs145354191 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230345 | TTCAAACTGATGAGC[A/C]CAAAGAAACATAGTT | 50717 |
rs145383018 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227003 | GAAGATTTTCCCTTC[A/G]CCCTTTAGAATCTCT | 50717 |
rs145493075 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244094 | TGGGAAAGAAGACAA[C/T]AGGGACAAGGAGATT | 50717 |
rs145569672 | in-del | -/CT | 0.119281 | 0.213102 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230015 | GTAATAAGAGTAAAA[-/CT]CTGTCTAAAAAAAAA | 50717 |
rs145599821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248744 | AACTAAATAATTATC[A/G]CGAGCTGGATATGGT | 50717 |
rs145648849 | in-del | -/CC | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219687 | TGGGTAAATTCACTG[-/CC]AACAAGGCAAAAGAA | 50717 |
rs145691035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249941 | ACTTTCTGGAAAAGA[C/T]AAAACTATAGGAATA | 50717 |
rs145725509 | in-del | -/GGT | 0.147656 | 0.228091 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249050 | ACAAAATTAGCTGGG[-/GGT]GGTGGCACATGCCTG | 50717 |
rs145729712 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246358 | CAGACTGCCTGAACT[C/T]TTGACTCATAATTGC | 50717 |
rs145804942 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230808 | TCAGGCTGGAGTGCA[G/T]TGGCACAATCTTGGC | 50717 |
rs145856419 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260621 | TATGTTCTGACTCCC[-/T]TTTTGGCACCAACCC | 50717 |
rs145976316 | snp | C/T | 0.000379141 | 0.0137632 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218966 | GGGCTCAAGACAGTT[C/T]ACCTGGTCAGGAAGA | 50717 |
rs146043046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223038 | CCTATCAAGTAACCA[C/T]AGGCCTCTCTAATCT | 50717 |
rs146079183 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256589 | GAAGAAAAAAAAAAA[A/T]GGCACGTGAGGCAAA | 50717 |
rs146140364 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247363 | TTCTTGTCTTAATAA[C/G]AATAAAGCCTTAAAT | 50717 |
rs146166281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243063 | GAATTTAGCCTGTTA[C/T]CCTGACCTTCAAGGT | 50717 |
rs146188997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222137 | AGTACAAGAATATTC[C/T]AAGTAATCAAATCAA | 50717 |
rs146223482 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242007 | CAGCGCTTTGGGAGG[C/T]CAAGGCGGGTGGATC | 50717 |
rs146260378 | snp | A/G | 0.0111196 | 0.0737302 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215744 | GAAAAGCTTTACTGG[A/G]AGAAAATACAACAAA | 50717 |
rs146286375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261877 | GTACAAGACCACAAG[A/G]CAACAACCGACTCCG | 50717 |
rs146309615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242547 | TAGACAATTTTGGAG[A/G]CCTTACCACATTAAC | 50717 |
rs146381823 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160239082 | GATTAAGAAAGTAAA[C/T]ATAAATTTGCTACAA | 50717 |
rs146387156 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219839 | CTACCCCATCCAGAA[G/T]AGTTAGTTCCAGATC | 50717 |
rs146444030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236416 | TGTATATGTGTGTGT[A/G]TATATGTGTGTGTGT | 50717 |
rs146479814 | snp | A/G | 1.68604e-05 | 0.00290343 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217543 | GGAAAGGGTTGCCCA[A/G]GCAGGATCAGGTTGG | 50717 |
rs146600574 | snp | C/T | 0.000395948 | 0.0140648 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240070 | CGCTTGCGCTGTACA[C/T]GGCGCCGAGGCTGCT | 50717 |
rs146720622 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259039 | AATGGAGAATTTAGA[C/T]CCTGGATGATGGTAA | 50717 |
rs146888991 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240046 | GATGAGTCCTGGTCA[C/T]GGTTAGCCCGCTTGC | 50717 |
rs146913893 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259774 | TTACAACACGGCCAA[C/T]TCTGATCAGGTGTGC | 50717 |
rs147112905 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225508 | TGAAAGTCCAAGCTC[C/T]TCCCACCATACCAAC | 50717 |
rs147122039 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220740 | TCAAATCAGTCAGGA[G/T]ATCTGGGCAAGGCAG | 50717 |
rs147197863 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237718 | TTTTTTTTTGTTTGT[C/T]TTCCACAGATGGGGT | 50717 |
rs147356608 | in-del | -/C/CCCAA/CCCC | 0.0333954 | 0.124982 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234406 | TCATTTTCTCCTTTA[-/C/CCCAA/CCCC]CCCCTCTTTAGAGTC | 50717 |
rs147368853 | in-del | -/AA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256903 | AGAGATAAAAAAAAA[-/AA]CTGCTGCAAAGAAGT | 50717 |
rs147472335 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160233528 | AAAAGAATAACAGCT[G/T]CAGGGACAAAACTAG | 50717 |
rs147558082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245171 | CTCATCTTTCCTTAA[C/T]AAGGAATCAGGGTAT | 50717 |
rs147600854 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248041 | ATCTGAGCGGTGGTT[C/T]AGGCCTGTAATCCCA | 50717 |
rs147663666 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264327 | ACCAAGATTCTTGCA[A/T]TCATGGAACTTATTA | 50717 |
rs147871419 | snp | A/C | 1.70571e-05 | 0.00292032 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225170 | CCCCCCATTTGTTAT[A/C]CCATCTTCAGGAAAC | 50717 |
rs147875620 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239883 | GCGGAAACGCTGCAC[A/G]AAGACTCTTGCCCCA | 50717 |
rs147915192 | snp | C/G | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229965 | GAAGCGGAGGTTGCA[C/G]TGAGCCAAGATTGTG | 50717 |
rs147997856 | snp | A/G | 0.000247862 | 0.0111297 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240245 | TTTCTGTGCTGGTGC[A/G]GTTGGGGCCACCATC | 50717 |
rs148059542 | in-del | -/ACA | | | cds-indel, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239762 | GCCGTACCCAATCCC[-/ACA]CCACCACCTTCAGGT | 50717 |
rs148137107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220767 | GCAGAAAATAACTTC[C/T]AAGATCTTTGGTTCT | 50717 |
rs148174261 | snp | C/T | 0.000214477 | 0.0103534 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217640 | CTCCTCCTCGTCCGA[C/T]GTGTCTGAGGAGCTG | 50717 |
rs148266001 | snp | A/G | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232596 | CAGTGGACCAAGATC[A/G]TGCCACTGCACTCCA | 50717 |
rs148296226 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255384 | AGTAATCCTCCTACC[G/T]TGGCCTCCCAAAGTG | 50717 |
rs148327428 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242218 | CCACCGTACTCCAGC[A/T]TGGTAACAAGAGCAA | 50717 |
rs148402624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258284 | CCCAAGAGGTCGAGG[C/T]TGCAGTGAGCCATGA | 50717 |
rs148434500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244482 | CTCTGTACAACACTT[A/G]TTTTCACAACATAAA | 50717 |
rs148463630 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229793 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACCTGAG | 50717 |
rs148663581 | snp | C/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223245 | ATCTGTGCTTGCTAC[C/T]ATTAACAGGGCTCCA | 50717 |
rs148800813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247378 | GAATAAAGCCTTAAA[G/T]TTTTAACCAATTACA | 50717 |
rs148908968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248754 | TTATCGCGAGCTGGA[C/T]ATGGTGGCTCACACC | 50717 |
rs148918295 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259469 | ACCAGGGAGTCGGAG[G/T]TTGCAGTGGGCTGAG | 50717 |
rs149180197 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225909 | AGTGCAGTGGCATGA[A/C]CCCGGCTCACTGCAA | 50717 |
rs149235879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222079 | ATCTATTTGAATGTA[C/T]GCATGACATTTCACC | 50717 |
rs149289222 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229301 | ACTCTGTCTCAAAAA[A/G]AAAACAAAAATCTTC | 50717 |
rs149371678 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246230 | TGTTTTCCCACCTCC[A/G]TAATCAAAACTCTTT | 50717 |
rs149449388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261495 | ATCTAATTCTAATTA[C/T]TGAACAAATAACCCA | 50717 |
rs149826951 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243752 | AGTACAGCTCTGTTA[C/T]TGATATTTTGAAAAT | 50717 |
rs149865959 | in-del | -/TGT | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221316 | CCATTAAGACTCAAG[-/TGT]TGTTTTGGGTTTGTT | 50717 |
rs150007550 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217949 | TGCAAGCCAATGAAA[A/C/T]TTTATTTACAAAAAC | 50717 |
rs150017187 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264264 | AACTATTGAATTCCT[C/G]CTCTGGAAGGCCCTG | 50717 |
rs150349221 | snp | A/G | | | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239871 | CCCATGCTGCAGGCG[A/G]AAACGCTGCACAAAG | 50717 |
rs150468383 | snp | C/T | 4.94882e-05 | 0.0049741 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160225626 | TCTTGAGTACTCCAT[C/T]GTTCTCATTCTCATC | 50717 |
rs150470237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256549 | AACCCTATAGTAGCT[C/T]TCCAGATGGCTAAGA | 50717 |
rs150651690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238125 | CCTACCTTAAAACTG[A/G]CAGCTCTTAACTCCT | 50717 |
rs150694384 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256590 | AAGAAAAAAAAAAAT[G/T]GCACGTGAGGCAAAT | 50717 |
rs150713396 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254209 | TGCCTGTAATCCCAG[C/T]TACTGGGGAGACTGA | 50717 |
rs150783109 | snp | A/G | 8.39525e-05 | 0.00647836 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160238694 | TACTCGAACCTGCCC[A/G]TCACGGGCACACATG | 50717 |
rs150807874 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232722 | GCTCAGGAGGCTGAG[G/T]TGTGAGGATTCCTTG | 50717 |
rs150871644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247436 | AGAAAGACTTTACTA[C/T]GCTGGATAAGAGTAC | 50717 |
rs150980240 | snp | A/G | 0.030278 | 0.119257 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249176 | AGCCTGGGCAACAGA[A/G]GAGACTCCATCTCAA | 50717 |
rs151050731 | snp | C/G/T | 0.0003954 | 0.014055 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239976 | TTGCCAGCGAGGTCG[C/G/T]GGTAGAGCTGATGTT | 50717 |
rs151052932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224220 | CTCCTTATGTCCAAA[C/T]CAATTAGAAGCAACA | 50717 |
rs151106649 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230380 | TAGGCCAACTGGATA[C/G]GGATGGATACAGCTT | 50717 |
rs151169522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240763 | ATATAAAAAGAAGAG[C/T]CAACTCCAGCAAGAG | 50717 |
rs151332107 | in-del | -/AAAC | 0.487221 | 0.145683 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259531 | GCAAGACTCGTCAAA[-/AAAC]AAACAAACAAACAAA | 50717 |
rs180678680 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260811 | ACTAAAGGCAGCATC[A/C]CTCATCACTCCCCAG | 50717 |
rs180716275 | snp | A/T | 8.38357e-05 | 0.00647385 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239672 | GCCTGATTCTCTCAG[A/T]TGCTATTATGCTCCC | 50717 |
rs180716804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248563 | ACATAGTGAAACCCC[A/G]TCTTTACTAAAATAC | 50717 |
rs180860299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223707 | GTTAGAGACCAGCTT[C/G]GGCAACATGGTGAAA | 50717 |
rs180921360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232795 | TGTACTTCTGCTTAG[A/G]TGACAGAGTGAGACC | 50717 |
rs180929506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254436 | TGAATAATTTATATA[C/T]ATATGTTTATAAGAA | 50717 |
rs180954749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244629 | TATTCTTTCTTTTTT[A/T]TTTTTTGAGACAGAG | 50717 |
rs180997028 | snp | A/T | 0.00539807 | 0.051671 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216935 | GACCTATTTAGGGGG[A/T]GATGGGATGAAGAGA | 50717 |
rs181364443 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160245077 | GGGAAGAAAAAGGCA[A/T]CATTTCCATTAAACC | 50717 |
rs181396500 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217310 | AACCAGTTAACAAAA[C/T]AGGCTTCCCTCTCCT | 50717 |
rs181397416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217993 | ACTGCCAGTTTGCCA[A/G]CCCCTGAACTAGGCC | 50717 |
rs181511243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254053 | TCCTGGGATGGGTGC[A/G]TGGCTCATGCCTGTA | 50717 |
rs181582326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249967 | GAATAGAGGGATCAG[A/G]GATTGCCAGGGCTTG | 50717 |
rs181588862 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225929 | GCTCACTGCAACCTC[A/C/T]GCCTCATGGGTTCAA | 50717 |
rs181590098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244776 | GCGCCTGCCACCATG[C/T]CCACCTTTCTGTATT | 50717 |
rs181626424 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232066 | CGTGGTGGCGCATGC[A/C]TATCATCCCAGCTAC | 50717 |
rs182013840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259653 | GATGAGGATCACTGT[A/G]TAGCCCAACAAGAAG | 50717 |
rs182015746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237869 | AATAAAATCAATTCC[A/G]TACCCTTAAGTGCAG | 50717 |
rs182092432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227603 | CATATGATGCTAGAA[C/T]GGAGTTTGGCAAACT | 50717 |
rs182110365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250954 | CCGATCGAAACATCA[A/G]CGTGTAAATATTATT | 50717 |
rs182323092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226706 | TTTTTCTCCTTCCCC[C/T]TACAGTTACACTACT | 50717 |
rs182467741 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264023 | CCTCATGTCATCCTC[C/T]TCTATCCCCTTACTC | 50717 |
rs182600170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250382 | GAGGCAGGAGAATTG[A/C]CTGAACCTGGAAGGC | 50717 |
rs182623075 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160251204 | GCCACACAGTCCCAA[A/G]TTTCTCTTGGGAGGA | 50717 |
rs182627970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229058 | TAATCCCAGCACTTT[A/G]AGAGGCCGAGGTGGG | 50717 |
rs182689252 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160241971 | TTGCAGGCTGGGCGC[A/G]GTGGCTAACACCTGT | 50717 |
rs182811320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220383 | AAAATAAAAAAACAC[A/G]GGGGAACAATTCCTT | 50717 |
rs182814085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255178 | AAAGAATTCAGAGAG[C/T]TCCGTTAATATCTTC | 50717 |
rs182848210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233849 | TTGAACTCTGCAGGG[A/G]GCATGCAGAGGTGCT | 50717 |
rs183158943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256647 | CAGACTTCCTTAAAC[A/T]GTAACTTCAGAGGAT | 50717 |
rs183193596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261831 | ATTTGGGAGTTAGAG[A/G]AGGTAAACTAAGATA | 50717 |
rs183317755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255955 | CAGTATTTCAGACTA[C/T]GTCAGGAATGCACTC | 50717 |
rs183425907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241550 | CATTCTCTTAACTCA[C/T]AACAGTCAAGTCAAT | 50717 |
rs183432100 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262723 | TGATACTCTAAACAA[A/G]TGCGAGTTAGGGGCT | 50717 |
rs183438015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246523 | CCTGATGCTCACAGG[A/T]GTGGCATGCACCTGT | 50717 |
rs183480049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234764 | AAACATCATGTAGTT[A/C]AAAAGATTAAATGAT | 50717 |
rs183495872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253464 | ACAAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 50717 |
rs183526925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230685 | TATTTACTAATATAG[A/T]ACTTGCTGGTAAACC | 50717 |
rs183800634 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246000 | AAAATTAGCTGGGCA[C/T]GGTGGCACATGCCTG | 50717 |
rs183983624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253627 | CACTCCAGCCTGTGC[A/G]ACAGGGTGAGACTCC | 50717 |
rs183993086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249177 | GCCTGGGCAACAGAG[A/G]AGACTCCATCTCAAA | 50717 |
rs183993392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218707 | GGACTATTCCTACAG[A/T]GGAAATTACAGGAAT | 50717 |
rs184026407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224286 | CTCCTCTAGCATAGC[A/G]GAGAAAACATGAAAA | 50717 |
rs184026814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256968 | CTAATTTTTGAAAAG[A/C]TTTCAAAGACTTTCT | 50717 |
rs184083647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252566 | TATAATAAAAGCTTT[A/G]TTGTTGGGGGGCAGG | 50717 |
rs184178316 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217214 | CCCCTTGGTACTGAA[C/T]AGCCAGTTGTTCCCC | 50717 |
rs184311757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244654 | ACAGAGTCTCATTCT[A/G]TCGCCCAGGCTGGAA | 50717 |
rs184428063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247386 | CCTTAAATTTTTAAC[C/T]AATTACATGACAAAA | 50717 |
rs184668523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242728 | CTCAACTCCAGTATG[C/T]AGAACAAAAGCAACT | 50717 |
rs184796217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236330 | TGTGTGTATATAAAT[A/G]CATATGTGTGTATAT | 50717 |
rs184867648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231168 | AGATTTTTGGAAAAC[A/G]GTAAAAAATTCAAGA | 50717 |
rs184939709 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160215896 | GAGCTGCTGGGAAAA[A/G]GGGCAGGAGGAAGAA | 50717 |
rs184959279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244391 | AGAGTCTCAACTCAA[C/T]ACATAAAGCTAACTT | 50717 |
rs185038559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259219 | GTCATATTATTAAGA[C/T]GGTCCAGCTGTGGAG | 50717 |
rs185133814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237467 | ACAGTTGATTTGCTA[C/T]TTCAACTAAGTCCTC | 50717 |
rs185433079 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244778 | GCCTGCCACCATGCC[C/T]ACCTTTCTGTATTTT | 50717 |
rs185452508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254619 | CAACATGGTAAAACC[A/C]CATTTCTACTAAAAA | 50717 |
rs185458583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233594 | AAAGAGAGGAGGAGC[C/T]GATGCTGCTCCTTCC | 50717 |
rs185463390 | snp | C/G/T | 6.62004e-05 | 0.00575295 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217724 | CTGTGGATGGGAAAG[C/G/T]CTTGTTAGTAACTTC | 50717 |
rs185540560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247750 | TTCAGATTTTTTAAT[C/T]TGGGATGCTCAACTT | 50717 |
rs185608044 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223460 | AAATCATGACAGGTA[A/T]CTGCTAGGAGTGGTA | 50717 |
rs185720292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229842 | GCCTGGCTAACACGG[C/T]GAGACCTCGGTTCTA | 50717 |
rs185994727 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250007 | GAATGAAACTGACTA[C/T]GAAAGGGCATGAGAA | 50717 |
rs186000943 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226106 | TTAAGTGGCAATCCT[C/T]AATTCTGTCAGTTTG | 50717 |
rs186185838 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255429 | ATGTACCACCACACC[A/T]GGCCTCTTCTCCCTC | 50717 |
rs186270228 | snp | A/G | 4.94344e-05 | 0.00497139 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218305 | CTCCCTTGGGAATTC[A/G]TTTCCAACCCTAGCT | 50717 |
rs186345313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245098 | CCATTAAACCATCTC[A/G]TCCCATTTCATATAA | 50717 |
rs186360966 | snp | A/C/G | 8.24088e-05 | 0.0064186 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240047 | ATGAGTCCTGGTCAC[A/C/G]GTTAGCCCGCTTGCG | 50717 |
rs186432577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259704 | TGGCAAAAAAGGAAA[G/T]TATAAAGAATAGTTG | 50717 |
rs186439009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238939 | AAGGGAGAGAAAAAA[C/T]TTCCTTTGATGTAAG | 50717 |
rs186507007 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233929 | GAAACATTAAACAAA[G/T]TCACCAAATTTTGCC | 50717 |
rs186652520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261526 | CACACATATGGAAAT[A/C]AAATGAACCAACATG | 50717 |
rs186811001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256695 | TCTAAAATGTTTGCA[C/T]TGACCCAATCCACTA | 50717 |
rs186813638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235806 | TGCAGTGGCATGATC[C/T]CAGCTCACTGCAACC | 50717 |
rs186878228 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-5-prime, upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262560 | AGACTGAGGGAAGAG[C/T]GGTCGCGCGAGCTCA | 50717 |
rs187005360 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221521 | ACCCTTTCACCAGGG[C/G]AAGAAAAACATAAGG | 50717 |
rs187027841 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246780 | CCAGCCTGGGCAACA[C/T]AAGAAGACCCCCGTC | 50717 |
rs187077893 | snp | G/T | 1.79677e-05 | 0.00299725 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240421 | AAAATAAGAAAACAG[G/T]ATAGTGACCACCTTA | 50717 |
rs187186557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232364 | ATTATTATAAAAAGC[C/T]GGGTGCGGTGGCTCA | 50717 |
rs187244347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228144 | ATTGCCCAAGTTGGC[C/T]TTGAACTTCTGACCT | 50717 |
rs187253660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250955 | CGATCGAAACATCAA[C/T]GTGTAAATATTATTA | 50717 |
rs187341276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227031 | TCTGGCCTGTTTCAG[A/C]ATATAATGAAAACTC | 50717 |
rs187415436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254072 | CTCATGCCTGTAATC[C/T]CAACACTTTGGGAGG | 50717 |
rs187565517 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241569 | AGTCAAGTCAATTCC[A/T]ATGAGAACTTGAGGA | 50717 |
rs187573509 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263553 | CTGAGGCAGGAGAAT[A/T]GCTTGAACCCGGAGG | 50717 |
rs187613726 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160251252 | TCATAAATGAGCAGC[C/T]GTTCAGGGTTGATCT | 50717 |
rs187677710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242730 | CAACTCCAGTATGTA[C/G]AACAAAAGCAACTCA | 50717 |
rs187685170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220149 | GAATAAAACAGAAAC[C/T]CCGTTCTTTATCTCC | 50717 |
rs187962166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247483 | CAAGTGTCTCTTGTT[C/T]AAAACTACTGGGGCT | 50717 |
rs187988383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246130 | CTGGGCAACAAGAGC[A/T]AACTCCGTCTCAAAA | 50717 |
rs188034952 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242171 | AATCGCTTGAACCTG[C/G]GAGGTGGAGGCTGCA | 50717 |
rs188085339 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253579 | CTTGAACCTGGGAGG[C/T]AAAGGTTGCAGTGAG | 50717 |
rs188089715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230723 | ATGGCTTAGCTGCCA[C/T]GTGAGGACCTTGGTC | 50717 |
rs188319016 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260435 | CTAATTCAGTCATCA[A/G]ATGGAATAAAACTCA | 50717 |
rs188325348 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264161 | TTTTTATCATCTTTG[G/T]AATCTCAACACCTAG | 50717 |
rs188362621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224871 | AGCATTCTGCAAATG[A/G]TACCTGGCATCTCCA | 50717 |
rs188426187 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249682 | GTCCACAAAATTAAA[A/T]ATACCCTGTAGGTGA | 50717 |
rs188453255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239491 | CACCCTACCTATGAG[G/T]CTTCCAACAGTCCAC | 50717 |
rs188495659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229119 | CTGGCCAACATGGCA[A/C]AACCGTATCTCTACT | 50717 |
rs188587754 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252590 | GGGCAGGCAGTCAGG[A/C]ATCAGAGAAATTATT | 50717 |
rs188865647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234976 | TCTACTATCCAAACA[G/T]CTTTTTCTGGACTTA | 50717 |
rs188897971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230365 | GAAACATAGTTAAAA[C/T]AGGCCAACTGGATAG | 50717 |
rs189020411 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237700 | CCTGGCTAATTTTTT[A/C]GCTTTTTTTTTGTTT | 50717 |
rs189106639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256173 | AACTTTCTATAAAAA[C/T]ATCCAGGACCATTTA | 50717 |
rs189113289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244758 | AAGTAGCTGGGACTA[C/T]AGGCGCCTGCCACCA | 50717 |
rs189127918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222366 | TCATTTGGAAAAGGT[A/G]CACGTCTAGAGATAA | 50717 |
rs189272552 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216633 | GTAAACTGACCCCAG[A/G]TGTCACTTCCACACC | 50717 |
rs189284547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244517 | TGGGTCAGATTCTGA[A/G]TATCATTTTACACAC | 50717 |
rs189369416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223631 | AACACCAGGATTGGG[A/C]TTGGTGGCTCATGCC | 50717 |
rs189396245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257783 | GAGGCGCAATCTCAG[A/C]GCACTGCAGTGATCA | 50717 |
rs189402705 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217299 | TCCCTATCCCAAACC[A/C]GTTAACAAAATAGGC | 50717 |
rs189613953 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248184 | TGGTGGCACATGCCC[A/G]TAGTCCCTGCTACTG | 50717 |
rs189735606 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263949 | ACTAGACTTGAGGTG[G/T]CTATTGAAATCCTAC | 50717 |
rs189763883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254715 | AGGACTGCTTGAACC[C/T]GAGAGGGGAAGGTTT | 50717 |
rs189772226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160233726 | ATAGATTATGAAGTA[C/T]TGGCTCCACAGTTAT | 50717 |
rs190109918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251189 | TTATTAAGACAGAGA[A/G]CCACACAGTCCCAAG | 50717 |
rs190118116 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228463 | TTTAGCAATAAATTT[C/T]CATGTCAGCCAAATT | 50717 |
rs190146451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231180 | AACGGTAAAAAATTC[A/C]AGATAATAGTTAATG | 50717 |
rs190180247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259259 | GAACTCTTTGGCCGG[G/T]CATGGTGGTTCACAC | 50717 |
rs190275673 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254204 | GTGCATGCCTGTAAT[A/C]CCAGCTACTGGGGAG | 50717 |
rs190407244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253803 | TGCACTCCAGCCTGG[A/G]TGACAGAGCAAGTCC | 50717 |
rs190478873 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262635 | AGGCCAACGGAAAAC[A/G]GAGCGAGAGGCGCCT | 50717 |
rs190482851 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160240484 | AATGAACTTTGGTCC[A/C]AGTGTTTTCATTACA | 50717 |
rs190511166 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232523 | GTATGCACCTGTAAT[A/C]CCAGCTACTTGGGAG | 50717 |
rs190535422 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244779 | CCTGCCACCATGCCC[A/G]CCTTTCTGTATTTTT | 50717 |
rs190665427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217854 | TACTTTAGACTTGTG[A/G]TCTATATGGTCTTTA | 50717 |
rs190750823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245430 | TTCCCATGACAATTA[C/T]TCCAGAAGCAGCCTC | 50717 |
rs190776456 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246201 | GACCAGTGTAACATG[A/C/G]AGAACAGATCTGATG | 50717 |
rs190810179 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227088 | CATAAGCATACTTTC[A/T]GGAGGTTCACATAAT | 50717 |
rs191012422 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160220152 | TAAAACAGAAACCCC[A/G]TTCTTTATCTCCTCC | 50717 |
rs191031915 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261674 | CACAGAGCAGGGGGG[G/T]AAATCCCGGAGAGAA | 50717 |
rs191078405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250698 | GACTGCCTGTGTGAT[C/T]TATCAGCGACCATAT | 50717 |
rs191238981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235817 | GATCTCAGCTCACTG[A/C]AACCTCCACCTCCCA | 50717 |
rs191253478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256868 | TGAGAAATCTGGCTT[C/T]TGGCCCAGGAACTAT | 50717 |
rs191284703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241745 | GGAAAGGCAGACCAT[C/T]CAGTATGAGCTATTC | 50717 |
rs191293967 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230490 | AAGAGCCAGTGTTAA[C/G/T]AAAAGGTGTTCACGG | 50717 |
rs191317846 | snp | C/T | 1.67019e-05 | 0.00288975 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240133 | TCCTCTGAGCGGTCA[C/T]GGACTCGATTTTCAT | 50717 |
rs191485674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250160 | TATACCTTAATAAAC[A/G]TGGCCTAAAAAGAGC | 50717 |
rs191623446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234632 | TTTCACAACTCTTTA[A/G]CACAGCATATTAAAT | 50717 |
rs191741845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226222 | ATGTACATTACCTAC[C/T]GAAAAAGGTTACTCA | 50717 |
rs191789678 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253595 | AAAGGTTGCAGTGAG[C/T]CGAGATCGCACCATT | 50717 |
rs191797874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230895 | CAGCTGGGACTACAC[A/G]CATGTACCACCATGC | 50717 |
rs191844332 | snp | A/C | 0.00790255 | 0.0623604 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218489 | CAATGAAGAGGAACC[A/C]GGGACCTGATCAAGA | 50717 |
rs191884688 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255639 | ATTTTTATTTTTTTG[A/G]GACAGGGTCTCACTC | 50717 |
rs192112858 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | PEA15, DCAF8 | GRCh38.p7 | 1:160215528 | CCTAAGTATCACTGA[A/G]CTAAATGGAGTGTAT | 50717 |
rs192131000 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243441 | AAAAGACGGGGTCTC[A/G]CTATGTTGCCCAGGC | 50717 |
rs192156024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221605 | AAAACCTCATCAAGA[C/G]ATGGCTAGGCTCTTT | 50717 |
rs192169927 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246857 | GCTACTTGGGGTAGG[A/G]CTGAGATGGAAGGAT | 50717 |
rs192363818 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235268 | CCTCCTGAGTAGCTG[C/G]GATTATAGGCATGTG | 50717 |
rs192754126 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252673 | GTTTAAAAGCTATTA[C/T]AGTTGCCAAGATAAG | 50717 |
rs192882807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252498 | TGGTCAAGAAACATA[C/T]ATGGGTAGTCTACTT | 50717 |
rs192940235 | snp | A/G | 0.119281 | 0.213102 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236450 | TGTGTGTGTGTGTAT[A/G]TATATATATATCCTC | 50717 |
rs192976434 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242208 | CGAGATTGTGCCACC[A/G]TACTCCAGCTTGGTA | 50717 |
rs193131741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256480 | ATACCTGGTAATGTG[A/G]CAATCATTAAAGTAC | 50717 |
rs193137961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223185 | GTCATCAGCTGATCT[A/G]AGACTGATGAAGGTA | 50717 |
rs193153481 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229355 | GCCAATAGAGGAATA[C/T]TGAGGCTGATAAGAC | 50717 |
rs193179064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258433 | CTCTAATCATCCTAG[A/G]AAATACTACCTAATA | 50717 |
rs193288595 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247509 | GGGCTGCTCTTTTCC[G/T]CTAATATGATGAAAG | 50717 |
rs199572155 | snp | A/G | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240001 | GATGTTTCTGAGGAC[A/G]CCCAGTCCTCTAGGG | 50717 |
rs199646617 | snp | A/G | 1.74885e-05 | 0.00295701 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238577 | CAGAGGATTTGGATT[A/G]CACAAATTTTGGAGC | 50717 |
rs199664178 | snp | A/T | 0.131038 | 0.219882 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243424 | TTTTTTTTTTTTTTT[A/T]AAAAAGACGGGGTCT | 50717 |
rs199677055 | snp | A/G | 0.00023081 | 0.0107402 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240062 | GGTTAGCCCGCTTGC[A/G]CTGTACACGGCGCCG | 50717 |
rs199714661 | snp | C/G | 0.013653 | 0.0814869 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239745 | GTCCAGTACTGGCTG[C/G]CGCCGTACCCAATCC | 50717 |
rs199715178 | in-del | -/TATATT | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237738 | GGGTCTTGCTATATT[-/TATATT]GCCCAGGCTGGTCTT | 50717 |
rs199723721 | in-del | -/TGTG | 0.0325976 | 0.123435 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236398 | GTATATATGTGTACA[-/TGTG]TGTGTATATGTGTGT | 50717 |
rs199748027 | in-del | -/CTCTTCTTCCTC | 0.0323896 | 0.123068 | cds-indel, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240084 | ACGGCGCCGAGGCTG[-/CTCTTCTTCCTC]CTCTTCTTCCTCCTC | 50717 |
rs199822097 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218473 | TGGGAAGAGGGGGCA[A/G]CAATGAAGAGGAACC | 50717 |
rs199888208 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160229295 | GTCTCAAAAAAAAAA[-/A]CAAAAATCTTCACAT | 50717 |
rs199890713 | snp | G/T | 0.00199804 | 0.031544 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240426 | AAGAAAACAGGATAG[G/T]GACCACCTTAGTCTA | 50717 |
rs199917304 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248710 | CCATCTCAAAAAAAG[-/A]AAAAAAAAAAACTGT | 50717 |
rs199942558 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236305 | GTATATATATACATA[C/T]ATATATACGTGTGTG | 50717 |
rs200043571 | snp | A/G | 0.000395915 | 0.0140642 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240071 | GCTTGCGCTGTACAC[A/G]GCGCCGAGGCTGCTC | 50717 |
rs200095819 | snp | A/G | | | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160222725 | GGAAGATGTGCCCAC[A/G]GTCACTACCGCTCAC | 50717 |
rs200098593 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248308 | AGAGACTCCATCTAG[-/A]AAAAAAAAAAAATTA | 50717 |
rs200227775 | in-del | -/GAGGAAGAA | 0.0232847 | 0.105357 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160215903 | TGGGAAAAGGGGCAG[-/GAGGAAGAA]GTATCTGGGAATACC | 50717 |
rs200257711 | in-del | -/C | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236074 | AAAAAAATGGTGGGG[-/C]GGGGGTGACTGAGGG | 50717 |
rs200282728 | in-del | -/G | | | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160262239 | CCGGCTGGGAAGCGA[-/G]GGGGGGGCGCAGGCC | 50717 |
rs200283069 | in-del | -/GTGT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236403 | TATGTGTACATGTGT[-/GTGT]ATATGTGTGTGTATA | 50717 |
rs200288353 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160237702 | GGCTAATTTTTTCGC[-/T]TTTTTTTTTGTTTGT | 50717 |
rs200391112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241822 | TTATTGCCTAGTCAT[C/G]TGGATTAGAGCAGTA | 50717 |
rs200396167 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258615 | AAAAAAACAAACAAA[A/C]AAAAAAAAAACAACC | 50717 |
rs200399127 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160219763 | GTCCGAAAGGCACCC[A/C]ATGCCCCCTGCTGTC | 50717 |
rs200433557 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229054 | CTGTAATCCCAGCAC[-/T]TTTGAGAGGCCGAGG | 50717 |
rs200437421 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217539 | GACAGGAAAGGGTTG[C/T]CCAGGCAGGATCAGG | 50717 |
rs200458418 | in-del | -/AT | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236305 | TATATATATACATAC[-/AT]ATATATACGTGTGTG | 50717 |
rs200487674 | in-del | -/TG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236432 | ATATGTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 50717 |
rs200586987 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160235153 | TTGGTTTTTTTTTTT[-/T]GAGACAGTCTTGCTG | 50717 |
rs200596217 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160242245 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 50717 |
rs200707843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261737 | GACTCCAGTAACAAT[C/T]ATGAGTCAGAAATTC | 50717 |
rs200843224 | snp | C/T | 0.000197655 | 0.00993922 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160231339 | GCAAACTGGTGGGTA[C/T]TGGCAGGATTCACAT | 50717 |
rs200924591 | in-del | -/ATCC | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160229045 | TGGCTCACGACTGTA[-/ATCC]CAGCACTTTGAGAGG | 50717 |
rs200941524 | snp | G/T | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218897 | AGCTGTGGGTGCCCA[G/T]ATCTTCACATCATGG | 50717 |
rs201029750 | in-del | -/TA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236312 | ATACATACATATATA[-/TA]CGTGTGTGTATATAA | 50717 |
rs201053617 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260700 | AGACCAGCTACAAAA[G/T]AAAGAGCAGCCACTA | 50717 |
rs201056171 | snp | C/T | 3.30246e-05 | 0.0040634 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240302 | CTGAGGCCTCCACTT[C/T]AATGCCTGAGGATGT | 50717 |
rs201094668 | in-del | -/CT | 0.084364 | 0.187256 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232632 | GGTGGCAGAGGGAGA[-/CT]CTGTCTCAAAAAAAA | 50717 |
rs201218702 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160254061 | TGGGTGCGTGGCTCA[C/T]GCCTGTAATCCCAAC | 50717 |
rs201359662 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218326 | AACCCTAGCTTACCC[A/G]GTGATGGCGTCTCTG | 50717 |
rs201535712 | in-del | -/ATAA | 0.0648419 | 0.167978 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236324 | TATACGTGTGTGTAT[-/ATAA]ATACATATGTGTGTA | 50717 |
rs201559324 | snp | A/C/T | 0.000378913 | 0.0137593 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239843 | TATTGACACAACCAG[A/C/T]ATGGCCCTCAAGCCC | 50717 |
rs201644816 | snp | A/T | 1.65233e-05 | 0.00287426 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240247 | TCTGTGCTGGTGCGG[A/T]TGGGGCCACCATCAT | 50717 |
rs201747259 | snp | A/C | 0.000115337 | 0.00759312 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239880 | CAGGCGGAAACGCTG[A/C]ACAAAGACTCTTGCC | 50717 |
rs201805205 | snp | A/C | 9.95718e-05 | 0.00705521 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217749 | AACTTCCCTGGATGG[A/C]ACAAGGACAAGCCTG | 50717 |
rs201812393 | in-del | -/CC | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228910 | ATTCAGTTGGCTGCA[-/CC]CAGGAGAGGTGCCAG | 50717 |
rs201842159 | in-del | -/AATC | 0.0256215 | 0.110247 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236214 | TATAAGCTAAAACTT[-/AATC]AATTTCAGCCATGGT | 50717 |
rs201875040 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160254322 | ACGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 50717 |
rs201885969 | snp | A/G | | | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239874 | ATGCTGCAGGCGGAA[A/G]CGCTGCACAAAGACT | 50717 |
rs201972727 | snp | A/C | 1.65236e-05 | 0.00287429 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231251 | GGTAGTATACAATGC[A/C]TCAGTCTTACAAACT | 50717 |
rs202000695 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258757 | CCTATCTCTACAAAA[A/T]TAAAAAAAACTTTAG | 50717 |
rs202014482 | in-del | -/CAAAAAAAAA | | | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263475 | TCTCTACGAAAAATA[-/CAAAAAAAAA]AAAAAATTACCCGGC | 50717 |
rs202082974 | snp | G/T | 0.00199796 | 0.0315434 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217534 | CCTGGGACAGGAAAG[G/T]GTTGCCCAGGCAGGA | 50717 |
rs202099948 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160254322 | ACGAAACTCTGTCTC[A/C]AAAAAAAAAAAAAAT | 50717 |
rs202141036 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226611 | GTTTGATGATTATCT[-/A]ATTTCTCAACCTCTT | 50717 |
rs367592007 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160229318 | AAACAAAAATCTTCA[C/T]ATAACTTCTGCCCAG | 50717 |
rs367616947 | snp | A/G | 1.65162e-05 | 0.00287365 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224562 | GCTCTGCCAAGAACA[A/G]GAACATAGCAGTGAA | 50717 |
rs367687917 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160231728 | CTGCAGTCCAACACA[A/G]TAACAGCCAGTTATT | 50717 |
rs367699869 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160224763 | ATGCTCAAAAAGGTC[A/G]TACCCATTAACTCAG | 50717 |
rs367800745 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160243553 | CCAGCCATGTAATCT[A/C]TCTATCAAACTACTA | 50717 |
rs367822909 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160259483 | GGTTGCAGTGGGCTG[A/G]GATCGCGCCACAGCA | 50717 |
rs368013453 | snp | A/C | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239970 | GAGGGCTTGCCAGCG[A/C]GGTCGGGGTAGAGCT | 50717 |
rs368028669 | snp | C/G | 0.000252693 | 0.0112376 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225159 | TGATGCCCCACCCCC[C/G]CATTTGTTATACCAT | 50717 |
rs368043837 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234599 | TGAACCTGATCCACA[A/G]GATAAGATCTCACTC | 50717 |
rs368071810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224266 | GAGATGCTCTTGAGC[A/G]CTTTCTCCTCTAGCA | 50717 |
rs368125038 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160257341 | TGTTATGCAATAAAA[A/T]GTCTGGTTTGGATAC | 50717 |
rs368164596 | snp | C/G | 0.000721991 | 0.0189862 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239667 | CTCATGCCTGATTCT[C/G]TCAGTTGCTATTATG | 50717 |
rs368221948 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258714 | TGAGCCCAGGAGTTT[A/G]AGACCAGCCTAGGCA | 50717 |
rs368336121 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221817 | CTAATTCTAGGTCTC[-/A]AAAAAAAAAAAAAAA | 50717 |
rs368354350 | snp | G/T | 3.29696e-05 | 0.00406001 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240060 | ACGGTTAGCCCGCTT[G/T]CGCTGTACACGGCGC | 50717 |
rs368406465 | in-del | -/CTACCAGAAACCTGAAAGCCTCACG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260564 | AGCCTCTAGTCTCTG[-/CTACCAGAAACCTGAAAGCCTCACG]AAAACTGCATTTATA | 50717 |
rs368423134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230034 | GTCTAAAAAAAAAAA[A/T]CTATGGCTACACATT | 50717 |
rs368455966 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236043 | CGTGCCCTGCCCACA[A/G]TGGTTTTCAACAGCT | 50717 |
rs368545808 | snp | C/T | | | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264173 | TTGTAATCTCAACAC[C/T]TAGAAGAGGGCTACA | 50717 |
rs368652723 | snp | A/C | 1.67097e-05 | 0.00289043 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240127 | TCCTCTTCCTCTGAG[A/C]GGTCATGGACTCGAT | 50717 |
rs368680411 | snp | A/G | | | downstream-variant-500B | PEA15, DCAF8 | GRCh38.p7 | 1:160215491 | AAATACCCCAAGTGT[A/G]TACCCTCACCCCACC | 50717 |
rs368729932 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216098 | GTGACCAGTGATAAG[A/G]CAAGTGCCCAAGCTC | 50717 |
rs368833443 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160244159 | TGATTTGTGTATGCA[C/T]GCTTAACAGGTCTTC | 50717 |
rs368846535 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160239199 | AAGGAGTAAAATCTT[C/T]CCAGAATAACAACAG | 50717 |
rs368947935 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221120 | CATCAAACCCTGGCA[C/T]TGGCTGAGCTAAAAG | 50717 |
rs369037918 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222627 | GAGATTAGGGAGCCA[A/G]CCAGCTCAGCACACC | 50717 |
rs369087418 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232198 | CTGCGCAACAGAGCA[A/C]GACTGTCTCAAAAAA | 50717 |
rs369152117 | snp | C/G | 0.000208319 | 0.0102037 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238591 | TGCACAAATTTTGGA[C/G]CAAGGTCTTACTTAC | 50717 |
rs369225026 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252829 | AGTTCTTAGTCTGGC[A/G]CCCAGAGAAAATCAA | 50717 |
rs369267854 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231418 | GTTTCCTTTAAGAGT[A/G]GAAAAGCACAGAAAG | 50717 |
rs369279952 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252668 | AACAAGTTTAAAAGC[C/T]ATTATAGTTGCCAAG | 50717 |
rs369284266 | snp | A/G | 1.64925e-05 | 0.00287158 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218490 | AATGAAGAGGAACCC[A/G]GGACCTGATCAAGAA | 50717 |
rs369389334 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232824 | CCCTGTCTCAAAAAG[C/T]AAAAAAATAAAAAAC | 50717 |
rs369499745 | snp | A/G/T | 0.000115327 | 0.00759285 | utr-variant-5-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160244032 | ATGTTTGCTGTAGCC[A/G/T]GCCTGGGTTTGGGAG | 50717 |
rs369558092 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160222028 | AATTGCCACATTTGC[G/T]TTCTCCTTATATGTA | 50717 |
rs369573820 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253693 | TAGCAGGGTGTGGTG[A/G]TGTACACCTGTAGTC | 50717 |
rs369704572 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160237267 | ATGAGGTTTCTAAAT[A/G]TTAGAATTAGAGGTC | 50717 |
rs369842065 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246966 | CAGTCTCCAAAAAAA[-/A]TAAAAAATAAAAAAT | 50717 |
rs369859743 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160225491 | AATCCAGATGACTGA[C/T]TTGAAAGTCCAAGCT | 50717 |
rs369866330 | snp | C/T | 4.94189e-05 | 0.00497062 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218345 | ATGGCGTCTCTGTCT[C/T]AGGTGATGCATAAGG | 50717 |
rs369866840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248716 | CAAAAAAAGAAAAAA[A/G]AAAAACTGTCACAAC | 50717 |
rs369944779 | snp | C/T | 0.000121297 | 0.00778678 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225696 | ATGAAAATGTAAAAA[C/T]GTACAAACGAAACCC | 50717 |
rs370043097 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160250990 | CCTTGATCCCTTTAC[G/T]AAGACCTGAATTCGG | 50717 |
rs370224357 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261035 | GAAGACATGGGGCAG[A/G]GGGCACACATTCACT | 50717 |
rs370343151 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234036 | AATACCTCAAACTGG[C/T]TTCCACTGGCTAAAG | 50717 |
rs370370573 | in-del | -/AA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234256 | CAAAAAAAAAAAAAA[-/AA]AWGCCTCTGACATAA | 50717 |
rs370374204 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240007 | TCTGAGGACACCCAG[C/T]CCTCTAGGGCCCGCT | 50717 |
rs370547825 | snp | C/T | | | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262894 | TTTCAGGGCTTTGTT[C/T]CCTTAAGTGGTTTCT | 50717 |
rs370565412 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248660 | GTGAGCTGCGATCGC[A/G]CCACTGCACTCCAGC | 50717 |
rs370602448 | in-del | -/AT | 0.0123036 | 0.0774623 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236354 | TGTATATGTGTGTAC[-/AT]ATGTGTGTATATAAA | 50717 |
rs370613647 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240411 | AGGAGAGGGAAAAAT[A/T]AGAAAACAGGATAGT | 50717 |
rs370935045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160239170 | TGGCTGGTACCAGTA[A/C]AGTAGATGGGGCCAA | 50717 |
rs370936513 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228231 | ACCACACCAAGCCCC[C/T]TGACATTTTAAGTCA | 50717 |
rs370966751 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237808 | GCCTCCCAAAGTATT[A/G]GGATTACAGGCATAA | 50717 |
rs371042081 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160259311 | AGGCTGAGGCGGGCA[C/G]ATCACAAGGTCAGGA | 50717 |
rs371081800 | snp | A/G | 3.57194e-05 | 0.00422592 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238753 | GAAACTTGGCCTGGG[A/G]TGTTAAAAATGAAAA | 50717 |
rs371101550 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232659 | AAAAAAAAAAAAATT[A/G]TTATAAAAAATTAGC | 50717 |
rs371184326 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258864 | TTACCCAGCACATAA[A/G]GAAATAAACAGTCCA | 50717 |
rs371277260 | snp | A/G | 9.57167e-05 | 0.00691731 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237092 | TGGAATATGTTCAAG[A/G]CTAAGAGATACAGTT | 50717 |
rs371314738 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249008 | GCTGGCCTGACCAAC[A/G]TGGTAAAACCCCATC | 50717 |
rs371334994 | snp | A/G | 3.30207e-05 | 0.00406316 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225020 | GCAGCTCCCTAGACA[A/G]AGGGGGCATGCCAGC | 50717 |
rs371339023 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222624 | GGAGAGATTAGGGAG[C/G]CAGCCAGCTCAGCAC | 50717 |
rs371456521 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248605 | GCAGGCATGATGGTG[C/G/T]GTGCCTGTAATCCCA | 50717 |
rs371605503 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160244627 | ATTATTCTTTCTTTT[G/T]TTTTTTTTGAGACAG | 50717 |
rs371765593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229587 | TGGAATTTGTTAGAG[A/G]CACAGACTTTTCAAG | 50717 |
rs371783866 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236386 | CATATATGTGTGTGT[A/G]TATATGTGTACATGT | 50717 |
rs371810218 | snp | C/G | 1.67388e-05 | 0.00289294 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240139 | GAGCGGTCATGGACT[C/G]GATTTTCATCATTAA | 50717 |
rs371899676 | snp | C/T | 1.6727e-05 | 0.00289193 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239679 | TCTCTCAGTTGCTAT[C/T]ATGCTCCCTTGCCTC | 50717 |
rs371920109 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248239 | TGGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC | 50717 |
rs371944213 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160218366 | ATGCATAAGGAACCA[C/G]AGCATGTGACTATCA | 50717 |
rs371959381 | in-del | -/CA | | | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264241 | ATTCTTTCATTCATT[-/CA]GTCAACAACTATTGA | 50717 |
rs371966928 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160225961 | CAATTCTCTTGCCTC[A/G]GCCTCCTAAATAGCT | 50717 |
rs371987013 | snp | G/T | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217708 | CAGGTTCTCGCCAGC[G/T]CTGTGGATGGGAAAG | 50717 |
rs372143751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246025 | TGCCTGTAATCCCAG[A/C]TACTAGGGAGGGTGA | 50717 |
rs372153623 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216144 | GTCCTTAGATTAATG[A/G]CTTATTCCTCAATCC | 50717 |
rs372170052 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160255921 | CACCGTGCATGGCCT[C/T]TGGCTTTAATTCTAA | 50717 |
rs372244185 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220898 | CTGCTGGAAAATTAG[C/G/T]ACCAAAAAACAGAGC | 50717 |
rs372324214 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258053 | TTCTTATACATTTAA[C/T]TGACTGCATTTAGCA | 50717 |
rs372392042 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160235144 | TATAATAATTTTGGT[G/T]TTTTTTTTTGAGACA | 50717 |
rs372404233 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229124 | CAACATGGCAAAACC[-/G]TATCTCTACTAAAAA | 50717 |
rs372511473 | snp | A/G | 1.65037e-05 | 0.00287256 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224556 | CCAGGAGCTCTGCCA[A/G]GAACAAGAACATAGC | 50717 |
rs372533762 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262882 | ATCCCCGTTTCCTTT[C/T]AGGGCTTTGTTTCCT | 50717 |
rs372591399 | snp | A/G | 1.68119e-05 | 0.00289926 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225672 | ATAAATCCTACAGTT[A/G]GAAAAGCAATGAAAA | 50717 |
rs372647657 | snp | C/T | 0.000141811 | 0.00841935 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225704 | GTAAAAATGTACAAA[C/T]GAAACCCTTGAAGAG | 50717 |
rs372675855 | snp | A/G | 3.49272e-05 | 0.0041788 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240402 | AAGGAGTAGAGGAGA[A/G]GGAAAAATAAGAAAA | 50717 |
rs372710663 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249709 | GTGAATGTTTTAATA[A/G]TTTTACTTAAATTCA | 50717 |
rs372735246 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234960 | CAGTTGTAGAAATTC[C/T]TCTACTATCCAAACA | 50717 |
rs372780555 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246531 | TCACAGGTGTGGCAT[A/G]CACCTGTAATCACAG | 50717 |
rs372826571 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222513 | TCAGCACCTCCAGGC[C/T]AACTAGTCTTTTATG | 50717 |
rs372870493 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252271 | ACAAGAGATAAAAGT[A/G]TCTATCATTTTTTAA | 50717 |
rs372951414 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217387 | CACCTCTCCATAGAG[A/C]CCCATTCCAGGGCTC | 50717 |
rs373219630 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160257893 | TGCCCCATGCTTGGC[-/A]TTTTTTTTTAAACTT | 50717 |
rs373235551 | snp | A/G | 0.000164832 | 0.00907682 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218481 | GGGGGCAGCAATGAA[A/G]AGGAACCCGGGACCT | 50717 |
rs373324705 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249125 | AACCTAGAAGGCAGA[A/G]GTTGCAAGTGAGCTG | 50717 |
rs373346548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160241668 | AAGATTTTAAATGCT[A/G]CTCATGGGCCTCCTT | 50717 |
rs373407557 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261561 | TTAGAAGCCAGGCAA[A/G]TAATCTCCCAGCTCC | 50717 |
rs373432093 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217101 | GGGTTGCTGGGGGTG[C/G/T]GGGGGGAGCCAACTG | 50717 |
rs373444186 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249689 | AAATTAAAAATACCC[C/T]GTAGGTGAATGTTTT | 50717 |
rs373533022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160261255 | TCTGTCTTGAACTCA[A/G]GAATTTTAATGCCTC | 50717 |
rs373595833 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252910 | ATTTAAAATCCAAGC[A/C]GACATGTTAGGAAGG | 50717 |
rs373624817 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160240946 | GAGGCACGTGGATCA[C/T]GAGGTTAGGAGATCG | 50717 |
rs373676811 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239861 | GGCCCTCAAGCCCAT[G/T]CTGCAGGCGGAAACG | 50717 |
rs373805185 | in-del | -/GGT | 0.0023933 | 0.0345097 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229999 | CTGCACTCCAGCATG[-/GGT]AATAAGAGTAAAACT | 50717 |
rs373992466 | in-del | -/TATC | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252274 | AGAGATAAAAGTATC[-/TATC]ATTTTTTAAAAAGAT | 50717 |
rs373997433 | snp | A/G | 3.29538e-05 | 0.00405904 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244038 | GCTGTAGCCAGCCTG[A/G]GTTTGGGAGAGGAAG | 50717 |
rs374057832 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253597 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 50717 |
rs374148952 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160233066 | TTGGCTTTAGTTTTT[A/G]TTTTTAAGTCTAAGG | 50717 |
rs374271455 | snp | C/T | 1.68621e-05 | 0.00290358 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224414 | GCCAACAGGCTTGGG[C/T]CAAAGAAACCTAGGA | 50717 |
rs374310410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221324 | GACTCAAGTGTTTTG[C/G]GTTTGTTCACTGCAG | 50717 |
rs374322596 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252157 | AAACATGCTGTTACA[C/T]AACAGCATTGGTACC | 50717 |
rs374353736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235969 | GTCTCAAACTCCTGA[C/T]CTCAAGTGATCCACC | 50717 |
rs374514683 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160250970 | CGTGTAAATATTATT[A/G]TTGTCCTTGATCCCT | 50717 |
rs374558809 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160223663 | AGCACTTTGGGAAGT[C/T]GAGGCAGGCGGATCA | 50717 |
rs374592604 | snp | C/T | 5.37485e-05 | 0.00518376 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238754 | AAACTTGGCCTGGGG[C/T]GTTAAAAATGAAAAA | 50717 |
rs374596901 | in-del | -/GTT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221320 | TAAGACTCAAGTGTT[-/GTT]TTGGGTTTGTTCACT | 50717 |
rs374705027 | snp | C/T | 0.0001294 | 0.00804258 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160237175 | CAATGGTGAAAACAA[C/T]TGCATCTTCACCTGC | 50717 |
rs374758933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238981 | GTTGGCTCTGGAAGA[C/T]TGAACTGGCACATGA | 50717 |
rs374873494 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160234927 | TCCCCAAGCCTAAAA[-/A]CATTTCTATCTTTTA | 50717 |
rs374906516 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225047 | CAGCCTAGGAGCTGG[A/G]CCCTGCTCACGTACC | 50717 |
rs374982418 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160222172 | ATATTGAATACCATG[C/T]TATCTAATGTATAAA | 50717 |
rs375218090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247763 | ATTTGGGATGCTCAA[C/T]TTGTACCAGAATAAC | 50717 |
rs375267419 | snp | A/C/G | 0.000401779 | 0.0141688 | missense, synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239784 | CACCTTCAGGTCATC[A/C/G]CTGCCACTGGCCAGC | 50717 |
rs375384944 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160262414 | AGGCCCAGCCGCCCC[A/G]TCCACTGCCACCACC | 50717 |
rs375398336 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160246062 | GGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 50717 |
rs375438233 | snp | G/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160233676 | CAAACAAATACAAAA[G/T]TTACCATGTGGAAGC | 50717 |
rs375457119 | snp | C/G/T | 5.08e-05 | 0.00503963 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224407 | CTCCAAAGCCAACAG[C/G/T]CTTGGGCCAAAGAAA | 50717 |
rs375623049 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160238181 | GGCCTATATTCCCAG[C/T]TTTAAATAGGGCTTC | 50717 |
rs375804297 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252639 | TGGACTGAAATGAAG[A/G]AAAAGGAAAGAGAAA | 50717 |
rs375901469 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160249301 | GAATCCACTAAACAC[C/T]TATTTGAATGGTCAA | 50717 |
rs375918133 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160224633 | GGGGTGGGGCTTCTT[A/G]CCAGTAGTGCCCCCT | 50717 |
rs376054635 | snp | C/G | 3.36768e-05 | 0.00410333 | intron-variant, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160239661 | CTCTAACTCATGCCT[C/G]ATTCTCTCAGTTGCT | 50717 |
rs376089912 | in-del | -/TTC | 0.00636936 | 0.0560724 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232952 | GTGGCATGAGGAATA[-/TTC]TTCTCAGATCTAAGC | 50717 |
rs376143884 | snp | A/C/G | 5.18241e-05 | 0.00509017 | intron-variant | DCAF8 | GRCh38.p7 | 1:160238595 | CAAATTTTGGAGCAA[A/C/G]GTCTTACTTACCTTG | 50717 |
rs376238711 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160262479 | CCACCACCACCGCCT[C/T]CGCTCTCTGCGCTTG | 50717 |
rs376363619 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252753 | ATCAACATGAGAATC[A/G]TTGTAAAGGTAGATA | 50717 |
rs376384255 | snp | C/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160259656 | GAGGATCACTGTATA[C/G]CCCAACAAGAAGGAA | 50717 |
rs376402308 | snp | C/T | 5.58176e-05 | 0.00528258 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238777 | ATGAAAAAAAGGACA[C/T]ACAAAAGAAATGAGA | 50717 |
rs376443695 | snp | A/C/T | 0.000131844 | 0.00811827 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160224495 | TACTGGGCCCCATCA[A/C/T]TGTGAGAGGAGTTGA | 50717 |
rs376498212 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258021 | AGCCATGAGCCAGCC[A/G]CACTCAGCCTGGCAG | 50717 |
rs376611740 | snp | C/T | | | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240073 | TTGCGCTGTACACGG[C/T]GCCGAGGCTGCTCTT | 50717 |
rs376678771 | snp | C/G | 4.96537e-05 | 0.00498241 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225560 | GTTGAGTCAGGGAAG[C/G]CTGCAGCAACTGGCC | 50717 |
rs376694435 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236229 | AATCAATTTCAGCCA[C/T]GGTGTTAAACATTAT | 50717 |
rs376887978 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160227374 | AGCTCACACGATCCT[C/T]CCGCCTCAACCTGCC | 50717 |
rs376903629 | in-del | -/CAAT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160236217 | AAGCTAAAACTTAAT[-/CAAT]TTCAGCCATGGTGTT | 50717 |
rs376943891 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160229883 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGTGCACC | 50717 |
rs376957899 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253972 | GAATGGAATGCTGAT[G/T]TTCTCTCCAGTAAAG | 50717 |
rs376966116 | snp | A/G | 5.11017e-05 | 0.00505453 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225683 | AGTTGGAAAAGCAAT[A/G]AAAATGTAAAAATGT | 50717 |
rs377066554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160251105 | CCTACATAAACACCC[A/G]TATTTAAATGAGACA | 50717 |
rs377300581 | snp | C/G/T | 3.29561e-05 | 0.00405921 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218456 | CTGGAACCCAAAAAG[C/G/T]TTGGGAAGAGGGGGC | 50717 |
rs377306445 | snp | A/G | 0.000330207 | 0.012845 | missense, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160240077 | GCTGTACACGGCGCC[A/G]AGGCTGCTCTTCTTC | 50717 |
rs377411496 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244842 | ATGGTCTCGATCTCC[C/T]GAGTGATCCGCCCGC | 50717 |
rs377530193 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217107 | TGGGGGTGGGGGGGG[-/G]AGCCAACTGTCATAA | 50717 |
rs377579019 | in-del | -/AATG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160245115 | CCATTTCATATAATG[-/AATG]GCAAACACTGTTTCA | 50717 |
rs377612770 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160233313 | CAGCACTTTGGGAGA[A/C]TGAGGTGGGAGGATC | 50717 |
rs377670764 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252933 | TAGGAAGGTACTGAC[A/G]AACAAATTTAAGTTT | 50717 |
rs386368468 | in-del | -/TT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228611 | CTCCTCTACTTACCT[-/TT]TTTTTTTTTTTTTGG | 50717 |
rs386368469 | in-del | -/TT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228623 | CCTTTTTTTTTTTTT[-/TT]TGGCCACAGGCCAAA | 50717 |
rs386368471 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160250486 | AAAAAAAAAAAAAAA[-/A]CAGGATGAGAGAAGA | 50717 |
rs386636033 | multinucleotide-polymorphism | AA/GT | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228892 | AAGGAGAAACCTCAA[AA/GT]CATTCAGTTGGCTGC | 50717 |
rs386636034 | multinucleotide-polymorphism | CAC/TGG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160244778 | GCCTGCCACCATGCC[CAC/TGG]CTTTCTGTATTTTTA | 50717 |
rs386636035 | multinucleotide-polymorphism | ACG/GCA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160250421 | CGGTGAGCCAAGATC[ACG/GCA]CCATTGCACTCCAGC | 50717 |
rs386636036 | in-del | AT/CAG | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160261218 | TATGACTTTAGTGGT[AT/CAG]CAGTTGAGCATCAGC | 50717 |
rs397721367 | in-del | -/A | 0.375 | 0.216506 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256040 | AAGACCTTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 50717 |
rs397755542 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228106 | ATTTTTTTTTTTTTT[-/T]GGTAGAGACACAGTC | 50717 |
rs397797458 | in-del | -/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258766 | TTTATCTTTCTAAAG[-/T]TTTTTTTTATTTTTG | 50717 |
rs397818833 | in-del | -/TG/TT/TTG | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228624 | CTTTTTTTTTTTTTT[-/TG/TT/TTG]GGCCACAGGCCAAAA | 50717 |
rs397938118 | in-del | -/A | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256588 | GAAGAAAAAAAAAAA[-/A]TGGCACGTGAGGCAA | 50717 |
rs527262738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240722 | TGGATGGGCATTTAT[G/T]AAGTTATAGCAAATA | 50717 |
rs527321415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247640 | AGTGGAGCATCTCAA[A/G]TCAGAAAATTCAAAA | 50717 |
rs527336855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224836 | GGGCTTCAGGACAGG[A/C]CCTGCCAAATATCAT | 50717 |
rs527383803 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264408 | GTTATAAAGAGTACT[A/G]TAAAGGAAAATAAAG | 50717 |
rs527400720 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217013 | AGAGAATGAATAAGG[G/T]GGAAAGGAAAGTGAA | 50717 |
rs527401262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160225771 | GATGCAGATAAACAA[C/T]ATTTTCCAAACCAAG | 50717 |
rs527442078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254237 | TGAGGCAGAAGAATC[A/G]CATGAAACTGGAAGG | 50717 |
rs527477659 | snp | C/T | 0.000421007 | 0.0145026 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217555 | CCAGGCAGGATCAGG[C/T]TGGCAGCCCCAGCCT | 50717 |
rs527584172 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160226593 | CATCCTTCCAGGGAC[C/T]TTGTTTGATGATTAT | 50717 |
rs527595196 | in-del | -/ATTA | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245838 | AGAGTTTAAAATTAT[-/ATTA]ATTCCTATCAAGTGG | 50717 |
rs527722466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231212 | ATTCCTATAAAATTC[A/G]TAACTCTCCATAAAG | 50717 |
rs527789684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160239033 | ACTGTATCTAGCAGA[A/G]GAGAAAAGGAATAGA | 50717 |
rs527847364 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246070 | TTGAACCTGGGAGGC[A/G]GAGGTTGTGGTGAGC | 50717 |
rs527907527 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235137 | GATCTGTTATAATAA[C/T]TTTGGTTTTTTTTTT | 50717 |
rs527915884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245489 | ATAGAAATCTAAGCT[A/G]CTTCATTAAAAGTAT | 50717 |
rs527981831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252585 | TTGGGGGGCAGGCAG[G/T]CAGGCATCAGAGAAA | 50717 |
rs527997632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219429 | CCCCCAGAGAAGAGT[C/T]GGAGAACTATATTCA | 50717 |
rs528120368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227478 | CCCAGCTTGGTCTCA[A/G]ACTCCTGGCCTCAAA | 50717 |
rs528389886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222957 | ATATTCTCCCAAAGA[A/G]CTCGCTCCTTAGGGC | 50717 |
rs528450755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248417 | TTGATCAAGGACAGT[A/G]ACCAGAATATCCTTT | 50717 |
rs528453861 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160255344 | TCTCACTATCTTGCC[A/G]CGTGGTCTCAAACTC | 50717 |
rs528564927 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263178 | AGCCCAGGGTGCAAA[A/T]ATCTGACCCTTTCTC | 50717 |
rs528738953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234032 | GAAGAATACCTCAAA[C/G]TGGCTTCCACTGGCT | 50717 |
rs528784524 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160252959 | AGTTTGGAACTTAAA[C/T]AAAGTAAGGCCAGAG | 50717 |
rs528802122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232832 | CAAAAAGTAAAAAAA[C/T]AAAAAACCCAGCTTA | 50717 |
rs528868886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218637 | ATTCTTAAAGATGCT[C/G]CTTATCCCCATCCTA | 50717 |
rs528896449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235069 | TTTATATTTTACTTA[C/T]GTCCTATGTAAATCA | 50717 |
rs528910155 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160232959 | GAGGAATATTCTTCT[C/T]AGATCTAAGCATTCA | 50717 |
rs528930546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219284 | AAGAAGACAATGAAA[G/T]CCAGATGACCTCATT | 50717 |
rs528960351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234387 | TTTGGGCCTCCTTCT[A/C]CTCTTCATTTTCTCC | 50717 |
rs529047112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248727 | AAAAAAAAAACTGTC[A/G]CAACTAAATAATTAT | 50717 |
rs529106768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160248310 | AGACTCCATCTAGAA[A/T]AAAAAAAAAATTAAA | 50717 |
rs529243052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255128 | TAGGACACAGTCCCA[A/G]GTCTATGAAATCTGC | 50717 |
rs529251129 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160226727 | TTACACTACTGAAAA[A/G]AACAATCAACATTCA | 50717 |
rs529319362 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160262449 | CCGCCGCCATCTTAC[A/G]CTGGCCAGCGGCCGC | 50717 |
rs529389637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160220418 | CTTAAGACTAAGGAA[A/G]AAGCCAGTGGCAAGA | 50717 |
rs529473305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221242 | GGCAATAGCTTATGT[C/G]AAGAAAAAATTCACT | 50717 |
rs529486705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232754 | GTCCAGAAAGTTGAG[A/G]CTGCAGTGAGCCGTG | 50717 |
rs529551701 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232156 | TAGAGGCTGCAGTGA[A/G]CAGAGATCATGCCAC | 50717 |
rs529558149 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246411 | ATGATAAAAGTAAGT[A/T]GAATTAAATGTCAAA | 50717 |
rs529666328 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259440 | CGGGAGGTTGAGGCA[G/T]GAGAATCGCTTGAAC | 50717 |
rs529672527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160252001 | AAATTAATCTCTATT[A/C]CTACTGTGCTGAAGA | 50717 |
rs529736733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258996 | TCTCAACCCACCTCA[C/G]CACCACCCTGGAGAA | 50717 |
rs529816788 | in-del | -/A/AA | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260085 | GTATCAATGATGTGC[-/A/AA]AAAAAAAAAAAACCA | 50717 |
rs529819259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224017 | ATCTTGGGCTAGTTA[C/G]TACCACCATTCCTCC | 50717 |
rs529894027 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229433 | AGCCTTACTCTAACC[C/G]TGGGAAAGTATCAGC | 50717 |
rs530020656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236406 | TGTGTACATGTGTAT[A/G]TGTGTGTGTATATAT | 50717 |
rs530073962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244121 | GATTTAACAATGTAC[A/G]GGTTTTATCATTTTT | 50717 |
rs530123127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257931 | AGACAAGGTCTCAAT[A/G]TTGCCTAGGCTGGAC | 50717 |
rs530138280 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250659 | TGAAAACGAAAGTGC[C/T]GAAAGGATTTTTGCT | 50717 |
rs530185340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257428 | ATACAGTAGAAATAA[C/T]GGAGTAATGAATCTA | 50717 |
rs530245422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256775 | AATTACTCCCCAATG[A/C]CCTATTGGCAACCTC | 50717 |
rs530306157 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264215 | CTATTTAATGCCCCA[A/C]CGTCCTATTCATTCT | 50717 |
rs530378200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226070 | CAAACCCTTAAATCC[C/T]TTATCCACATACTTC | 50717 |
rs530381128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258108 | TCCCAGCACTCTGGG[A/G]GGCTGAGGCAGGAGG | 50717 |
rs530394761 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160243146 | TTCTCTAATTTAAAA[A/G]TTGGCTCAGAGGTGA | 50717 |
rs530642564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228699 | TAAACTAAAATTCAG[C/T]ATTAATGATGCAAAA | 50717 |
rs530823894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160243142 | CGGCTTCTCTAATTT[A/G]AAAGTTGGCTCAGAG | 50717 |
rs530859970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF8 | GRCh38.p7 | 1:160222890 | AAATCAGCTAGATTA[C/T]GCATGTTTAACAGAT | 50717 |
rs530892025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242305 | CTGGGCTAGGGGCTG[G/T]AAGAAAAAGTTATGA | 50717 |
rs530895534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249868 | ATCTCAAGTATGTTA[C/T]GGTAAGTGCAATAAT | 50717 |
rs531151741 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263348 | GTAAGGTCTGGCCGG[A/G]CGCGGTGGCTCATGC | 50717 |
rs531297756 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160239189 | AGATGGGGCCAAGGA[A/G]TAAAATCTTTCCAGA | 50717 |
rs531364198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246331 | AACCAAGCATCAACT[C/T]CTACAGGAGCCCAGA | 50717 |
rs531386535 | snp | G/T | 3.31746e-05 | 0.00407262 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217743 | GTTAGTAACTTCCCT[G/T]GATGGAACAAGGACA | 50717 |
rs531438360 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221873 | ACATCTTAAGAGCTG[A/G]TTGCTCTTCATTCCC | 50717 |
rs531497119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259310 | GAGGCTGAGGCGGGC[A/G]GATCACAAGGTCAGG | 50717 |
rs531570017 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160262105 | GCTCTTGGGGGCAAC[A/T]CCAGGGCTGACCTGA | 50717 |
rs531646610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160229820 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCTA | 50717 |
rs531705658 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253609 | GCCGAGATCGCACCA[C/T]TGCACTCCAGCCTGT | 50717 |
rs531756093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244781 | TGCCACCATGCCCAC[C/T]TTTCTGTATTTTTAG | 50717 |