SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1378 | snp | A/G | 0.182825 | 0.240806 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107506 | CATTCTGAAAGACCG[A/G]GAGCCTGGAGGTGTG | 25853 |
rs1052656 | snp | A/G | 0.48978 | 0.0707512 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087362 | ACATCCATAGCCCCC[A/G]TGGCTTTGAGGAGAA | 25853 |
rs1052694 | snp | C/T | 0 | 0 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086582 | ACAGGCTGTAGATTT[C/T]TTAGTTCTCACAGAA | 25853 |
rs1980886 | snp | C/T | 0.172351 | 0.237636 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101103 | GCTTGGGTGACAGAG[C/T]CAGAACCTGTCTCAT | 25853 |
rs1980887 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100919 | GGGTATGGTGGCTCA[C/T]GCCTTTAATCCTAGC | 25853 |
rs2275003 | snp | C/T | 0.493107 | 0.0583 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124862 | CTTCCTCTTTTCGTG[C/T]TCCTTTTTTCACTCA | 25853 |
rs2296897 | snp | C/T | 0.44486 | 0.156619 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089397 | AGCAGTCATCTCAGG[C/T]AGGGGCTTACGCACC | 25853 |
rs2297609 | snp | A/C | 0.097727 | 0.198275 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126790 | CCCTAGATCCCGCCC[A/C]TCTCGTTCCGGCGGT | 25853 |
rs2769704 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097487 | aggcagatcacaagg[C/T]caggagtttgagact | 25853 |
rs2890539 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099360 | cctgtagtcccagct[A/G]caggctggggcagga | 25853 |
rs3061496 | in-del | -/A/AA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101064 | aaaaaaaaaaaaaaa[-/A/AA]GTTGGGGAGGGTTTG | 25853 |
rs3814509 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125495 | TTGACTTTCAGCCCT[C/T]GTAATTCACATTGGT | 25853 |
rs4878553 | snp | G/T | 0.326506 | 0.238006 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108310 | CTGTTCTAAGTGTTA[G/T]GAACACAGCTATGAA | 25853 |
rs4879741 | snp | C/T | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104445 | AGTTGGAAAGATAGG[C/T]GTGGGCCTTGTATGC | 25853 |
rs4879742 | snp | C/T | 0.334182 | 0.235401 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104990 | TCTCATATTAACCAA[C/T]TAAAAAATATGGGCC | 25853 |
rs4879743 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108326 | GAACACAGCTATGAA[C/T]GAGAGAAATAATATC | 25853 |
rs4879744 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108623 | atggtgaaaacccta[C/T]taaacttacaaaatt | 25853 |
rs4879745 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111724 | AGTCCAAAGGCTAGA[C/T]TGGACTAGGCCATTC | 25853 |
rs4879747 | snp | A/G | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118901 | ACCTGGGAGGCGGAG[A/G]TTGCAGTGAGCCAAG | 25853 |
rs4879748 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121848 | CTCAGGAGGCTGAGG[C/T]GGGAGAATCGATTGA | 25853 |
rs4879749 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122569 | acaacctccgcctcc[C/T]gggttcaagcaattc | 25853 |
rs5897559 | in-del | -/T/TT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101085 | TTTTTTTTTTTTTTT[-/T/TT]AAATGAGACAGGTTC | 25853 |
rs7022361 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103490 | TACCCATACACAAAG[A/T]TGTTTATTCGGAACA | 25853 |
rs7030120 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115433 | cgtctctactaaaaa[A/T]acaaaaaattagccg | 25853 |
rs7032075 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112674 | gaggccgaggagggc[A/G]gatcatctgaggttg | 25853 |
rs7044522 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115435 | tctctactaaaaata[A/C]aaaaaattagccggg | 25853 |
rs7047316 | snp | A/G | 0.0551013 | 0.156571 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128302 | gtagcctaggctgga[A/G]tgcagtggcacgatc | 25853 |
rs7470431 | snp | C/T | 0.331642 | 0.236293 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124376 | TGACTTATTTTATCC[C/T]GGCCTATAATTGGGT | 25853 |
rs7846909 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116862 | gacgggtgtgtaatc[C/T]cagctactcgggagg | 25853 |
rs7853415 | snp | C/T | 0.185155 | 0.241444 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095719 | ctggattagggatga[C/T]caatttgTATTGTAA | 25853 |
rs7857551 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096599 | TCAGAGCGAGACTCT[A/G]CCTCAAAAATAAATG | 25853 |
rs7862025 | snp | C/G | 0.391954 | 0.205789 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090649 | TTGCATACATTATTA[C/G]AGCCAAACCTATTTA | 25853 |
rs7862209 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090940 | tgggattacaggcat[C/G]agccaccgtgcccgg | 25853 |
rs7865341 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091220 | tagtcccagctactc[A/G]ggaggctaaggcagg | 25853 |
rs7871667 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115354 | cccagcactttggga[A/G]gccgaggcgggcgga | 25853 |
rs7875653 | snp | C/T | 0.267908 | 0.249358 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116306 | aggctgcagagatcg[C/T]gccactgaactccag | 25853 |
rs7875661 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109667 | GCTGGTTGTCCTGTA[C/T]GGTCTGGATGAGTCC | 25853 |
rs7875858 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088998 | cctgtggtcccagct[A/T]cttgggaggctgagg | 25853 |
rs10122086 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093129 | gctgggattacaggc[A/G/T]taagccaccacgcct | 25853 |
rs10123087 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094724 | tttagtagagacggg[G/T]tttcaccatgttagc | 25853 |
rs10511914 | snp | C/T | 0.480697 | 0.0963277 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107234 | TGCCCCTTTATCAAA[C/T]ATACACTGTGCCCTA | 25853 |
rs10511915 | snp | A/G | 0.266754 | 0.249438 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107312 | TAATCACTGAGACCC[A/G]TTTAAAAACAAGGCT | 25853 |
rs10511916 | snp | C/G | 0.39709 | 0.20215 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124314 | TCATTTGCCAGTCTT[C/G]TGACATCATGCTATT | 25853 |
rs10624115 | in-del | -/CAACAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102677 | AACAAACAACAACAA[-/CAACAA]AAAACAAGAACACTT | 25853 |
rs10738923 | snp | A/T | 0.492137 | 0.0622048 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108802 | TGGTCTCAAAAAAAA[A/T]AAATAAATAAATATA | 25853 |
rs10738924 | snp | A/T | 0.498652 | 0.0259235 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108806 | CTCAAAAAAAATAAA[A/T]AAATAAATATATATA | 25853 |
rs10758240 | snp | C/T | 0.469839 | 0.119042 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098112 | CCCACAAATATAGAC[C/T]ACTCAGAGAAATACT | 25853 |
rs10758241 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108812 | AAAAATAAATAAATA[A/T]ATATATATATATATA | 25853 |
rs10814069 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101262 | TTTCATTTTTTTGTA[A/G]AAATGGGGTCTCACT | 25853 |
rs10971903 | snp | C/T | 0.240765 | 0.249829 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087248 | AGCACTCACTACACA[C/T]AGATAAACCCCCTGC | 25853 |
rs10971904 | snp | C/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089945 | TAACTCTAAGCTTTT[C/G]TCCATCATATGTTTC | 25853 |
rs10971905 | snp | G/T | 0.392511 | 0.205404 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091423 | AGGCTGAGGTGGGTG[G/T]CCCAAGAGTTTGAGA | 25853 |
rs10971906 | snp | A/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092779 | GGTGGCTCCCAACAA[A/T]GGCTTCTGTGGCCAC | 25853 |
rs10971907 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092970 | cctgcctcagcctcc[C/T]gagcagctgggatta | 25853 |
rs10971908 | snp | C/T | 0.480775 | 0.0961398 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092974 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 25853 |
rs10971909 | snp | A/G | 0.481573 | 0.0972063 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093092 | GACCTCAGGTGATCC[A/G]CCCGCCTCGGCCTCC | 25853 |
rs10971910 | snp | C/T | 0.392511 | 0.205404 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096875 | GGTCAGGGTCCTTTA[C/T]TCCTGTCTCGTGATG | 25853 |
rs10971911 | snp | C/T | 0.393065 | 0.205018 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097063 | TTAAAGCAGGGCACA[C/T]ATGTGAAGGACAGTT | 25853 |
rs10971912 | snp | A/G | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100238 | gagtctcacactgtc[A/G]cccaggctggagtgc | 25853 |
rs10971913 | snp | C/G | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100868 | AGTCTTGAACCCCTG[C/G]CCTCAAGTGATCCTC | 25853 |
rs10971914 | snp | A/G | 0.408871 | 0.193029 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101592 | AGACGGGGTTTCTCT[A/G]TGTTGTTCAGGCTGG | 25853 |
rs10971915 | snp | C/G | 0.39214 | 0.205661 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103620 | gcacttcgagaggct[C/G]aagtgggaggatcgc | 25853 |
rs10971916 | snp | A/C | 0.408359 | 0.193449 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105822 | ggcgcgatctcagct[A/C]actgcaacctctgcc | 25853 |
rs10971917 | snp | C/T | 0.397183 | 0.202082 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106412 | GCCACATCAAAAGCT[C/T]CCTATAAAAGGGCAA | 25853 |
rs10971918 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108831 | tatatatatatatat[A/G]aatgaggtggacaag | 25853 |
rs10971919 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109326 | GAAGGCTTTGTGCCA[A/G]AAAATGGCTGTGAAC | 25853 |
rs10971920 | snp | C/G | 0.480697 | 0.0963277 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110848 | CTCTACTATCATCAC[C/G]TCTTGCCATGGACTT | 25853 |
rs10971921 | snp | A/G | 0.381891 | 0.212379 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111004 | TTTTTTTTTTTTTTT[A/G]AGACCAAGTCTTGCT | 25853 |
rs10971922 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112334 | agcgtggtggttcac[A/G]cctgtaatcccagta | 25853 |
rs10971923 | snp | C/T | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113541 | GACAGGGTTTCACCA[C/T]ATTAGCCAGACTGGT | 25853 |
rs10971924 | snp | A/G | 0.47726 | 0.104176 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113796 | CCGAAGTGTGCATCA[A/G]TGAATAAATGCATAA | 25853 |
rs10971925 | snp | A/G | 0.144632 | 0.226711 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113969 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTACCT | 25853 |
rs10971926 | snp | A/T | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114115 | CTCCGTCTCAAAAAA[A/T]AAAATGTGGCACAGA | 25853 |
rs10971927 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115402 | cgagaccatcctggc[C/T]aacatggtgaaaccc | 25853 |
rs10971928 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115418 | aacatggtgaaaccc[C/T]gtctctactaaaaat | 25853 |
rs10971929 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115437 | tctactaaaaataca[A/G]aaaattagccgggcg | 25853 |
rs10971930 | snp | C/T | 0.350982 | 0.228698 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116085 | AAATAAATCCAGGGC[C/T]GGGTGCGGTGGCTCA | 25853 |
rs10971931 | snp | G/T | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116228 | CGGGCATGGTGGCAG[G/T]CGCCTTTAATCCCAG | 25853 |
rs10971932 | snp | C/G | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116837 | AATACATAAATTAGC[C/G]GGGCACAGTGACGGG | 25853 |
rs10971933 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117073 | CCTACACAAGATGGA[C/T]TACACTACTAGCTAG | 25853 |
rs10971934 | snp | C/T | 0.258565 | 0.249853 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117712 | CTGAGGTTGGGATTT[C/T]GAGACCAGCCTCACC | 25853 |
rs10971935 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118147 | TTTTTTTTCCAAGAT[A/G]GAAAAAAAGACAGAC | 25853 |
rs10971936 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118988 | AAATAATAATAATAA[C/T]AATATCTCTCTTATC | 25853 |
rs10971937 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120688 | AAAAAAAAAAAAAAA[A/G]AAAACAAAGCAACCC | 25853 |
rs10971938 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120722 | CATAATGGGTTAGCC[C/T]GATACTCTCAGGTAG | 25853 |
rs10971939 | snp | A/C | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123437 | TTTGCAGATGCAAAA[A/C]CAAAAGCACAAATAA | 25853 |
rs10971940 | snp | A/G | 0.171899 | 0.237487 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127213 | TGCCCAGCACAACCA[A/G]CCCAGGCCGCCCTAC | 25853 |
rs10971942 | snp | A/C | 0.479421 | 0.0993283 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127765 | AGTTACCTGCTGGTC[A/C]CTTCAGGCTTCAGGC | 25853 |
rs10971943 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128429 | CTAATTTTTTTTTTT[C/T]TTTTTTGAGACGGAG | 25853 |
rs11557154 | snp | A/G | 0.295771 | 0.245774 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107507 | CCATTCTGAAAGACC[A/G]GGAGCCTGGAGGTGT | 25853 |
rs11788468 | snp | C/T | 0.487007 | 0.100199 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115078 | AGGAAAGTAATTCTA[C/T]GCAGGTCACACAGAC | 25853 |
rs11790791 | snp | C/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119625 | TCCTTTGGATAAATT[C/T]TCAGGTGTGAACATT | 25853 |
rs11793082 | snp | C/T | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088703 | AACGTTAGAGAAGAA[C/T]GGAGCAGCTGAAGAA | 25853 |
rs11794829 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119854 | ccaaaggcacaagcc[A/C]ccatgcccagctaat | 25853 |
rs12002910 | snp | A/G | 0.29278 | 0.246313 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091466 | acatgatgagaacct[A/G]tctctacaaaaatac | 25853 |
rs12337902 | snp | C/T | 0.279991 | 0.248195 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105113 | gaaaaattagcctgg[C/T]gtggtggtgggcacc | 25853 |
rs12346581 | snp | A/G | 0.0733688 | 0.176922 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127721 | GGATGCTCTTGCTTG[A/G]GGCTGATTGGCCTCA | 25853 |
rs12347013 | snp | A/C | 0.293037 | 0.246268 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105132 | gtggtgggcacctgt[A/C]atcccagctactcag | 25853 |
rs12351094 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101092 | tttttttttaaatga[A/G]acaggttctggctct | 25853 |
rs12351200 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108808 | caaaaaaaataaata[A/T]ataaatatatatata | 25853 |
rs12375716 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100034 | TTGGACCCCCTTATG[C/T]CTCTCtttttttaga | 25853 |
rs12376123 | snp | A/G | 0.0182019 | 0.0936463 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087632 | GACAGGTAGGGCTGG[A/G]TCACTTTGCAGTCCT | 25853 |
rs12376939 | snp | A/C | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110139 | AGAAGGGGACAAACC[A/C]CTCTCAAACTGGCAA | 25853 |
rs12379086 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093009 | cgccactgcgcccgg[C/G]taattttgtattttt | 25853 |
rs12379544 | snp | C/T | 0.105569 | 0.204058 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094809 | tgctgggattatagg[C/T]gtgagccaccgcacc | 25853 |
rs12379730 | snp | C/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100072 | tctcactttggggcc[C/G]agggtagacagggca | 25853 |
rs12551373 | snp | A/G | 0.428484 | 0.175052 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092432 | GTGGCTCACGCCTGT[A/G]ATCTCAGCACTTTGG | 25853 |
rs12551419 | snp | C/T | 0.477515 | 0.103619 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111263 | TGCCGGCATTACAGG[C/T]GTGAGCCACCGCACC | 25853 |
rs12551453 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111622 | GCCCCCACATCCCTG[C/T]GAGGGTGAGGCTCTG | 25853 |
rs12553049 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109530 | ACCTCCTCCGTGCAC[A/G]TACGGCCCCTGAACA | 25853 |
rs13293614 | snp | A/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108814 | aaataaataaataaa[A/T]atatatatatatata | 25853 |
rs13297057 | snp | C/T | 0.276534 | 0.248588 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128342 | tgcaacctctgcctc[C/T]tgggttcaagtgatt | 25853 |
rs13298362 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128428 | gctaatttttttttt[C/T]cttttttgagacgga | 25853 |
rs13300446 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097279 | ttttttttttttttt[C/T]gagatggagtcttgc | 25853 |
rs13301893 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113382 | ttttttctgaaacag[A/T]gtctagctctgtcac | 25853 |
rs13302272 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113383 | tttttctgaaacaga[A/G]tctagctctgtcacc | 25853 |
rs13302634 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103096 | cgagaccttaactcc[A/C]aaaaaaaaaaaaaaa | 25853 |
rs16935392 | snp | C/G | 0.350394 | 0.228956 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093276 | CTGAGGTGCACACAG[C/G]GACTCTTACCACTGC | 25853 |
rs17341977 | snp | C/G | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098259 | ATGGGGAAGGAAAAA[C/G]GAGTGCATATCCCAA | 25853 |
rs28364824 | snp | C/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125375 | TGTTGTTTGTAAATT[C/T]TGCAGTATGAGTTAT | 25853 |
rs28445766 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112606 | CTCAAAAACAAAAAA[A/T]AAAAAATATTGGCTG | 25853 |
rs28464797 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112605 | TCTCAAAAACAAAAA[A/C]TAAAAAATATTGGCT | 25853 |
rs28804127 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095206 | CAGCCTCCCAAGTAT[C/T]TGGGACTACAGACGC | 25853 |
rs34066464 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106039 | GGTGTGAGCCACCAC[-/C]ACCCGGCCTATATTT | 25853 |
rs34136603 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105768 | CCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 25853 |
rs34256400 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118139 | TTCTTTTGTTTTTTT[-/T]CCAAGATGGAAAAAA | 25853 |
rs34360829 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114109 | TCTCAAAAAAAAAAA[-/A]TGTGGCACAGATACA | 25853 |
rs34413097 | in-del | -/C | | | frameshift-variant | DCAF12 | GRCh38.p7 | 9:34089450 | TTTCAGATTCTCCCC[-/C]TGCTAGTCTGGGCTT | 25853 |
rs34456166 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103118 | AAAAAAAAAAAAAAA[-/A]AGAGAAACAACAGCT | 25853 |
rs34470601 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106037 | CAGGTGTGAGCCACC[-/C]ACACCCGGCCTATAT | 25853 |
rs34481024 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120204 | ATGAAAGTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs34660158 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122229 | ACACATATAATCAAA[-/A]CTTTGCAATTTTAGG | 25853 |
rs34868426 | in-del | -/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109578 | AGCCACAGAGGGGGG[-/G]TCCCACGCAGCCATC | 25853 |
rs34922785 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091661 | AAAAAAAAAAAAAAA[-/A]CCACAAAAAACCCAA | 25853 |
rs35213370 | in-del | -/AAAGA | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088025 | GAAGTAAGGGTGAGC[-/AAAGA]TATGTCATTTCAGCC | 25853 |
rs35359814 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110674 | TTTATGAACAGCTCA[A/G]GCAGCACAGTGAGAC | 25853 |
rs35442107 | in-del | -/C | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127363 | TCAGTCACCTTCCCC[-/C]TTACGGTGCAACTTC | 25853 |
rs35465638 | snp | C/T | 0.200801 | 0.245111 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090124 | GCTGGAGTGCAATGG[C/T]GCGATCTTGGCTCGC | 25853 |
rs35532392 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102778 | CAACCTGCAGCAAGG[-/A]AAATGTTATATTCCT | 25853 |
rs35755095 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119871 | CATGCCCAGCTAATT[C/T]TTAAATATTTTGTAG | 25853 |
rs35820744 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100216 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 25853 |
rs35852035 | in-del | -/AAAAAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103114 | AAAAAAAAAAAAAAA[-/AAAAAA]GAGAAACAACAGCTG | 25853 |
rs35856499 | in-del | -/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105011 | ATATGGGCCAATTTT[-/G]GGGAGGCCGAGGCAG | 25853 |
rs35866006 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118820 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA | 25853 |
rs35901122 | in-del | -/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126859 | GGCCATTTTCAACGG[-/G]TTGTTTGGCTACTGC | 25853 |
rs36066422 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095398 | TTTTTTTTTTTTTTT[-/T]GAGATAGGGTCTCGC | 25853 |
rs41313782 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087029 | ACATCACAGTCAGCT[A/G]CCTGCAAGTTTAAAA | 25853 |
rs41316005 | snp | C/G | 0.155987 | 0.23165 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088563 | CATGGGGCAGGAAAA[C/G]GGGGAGGAAGGGACA | 25853 |
rs41316007 | snp | C/T | 0.0263992 | 0.111815 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087784 | GACTAGTCCCAAAGC[C/T]GGACTCTGTGAATAA | 25853 |
rs45471992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126202 | CTCCAGTTAACGAGG[A/G]TCCAGTCCTGACCCT | 25853 |
rs55646279 | snp | C/T | 0.079617 | 0.182947 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101977 | GCTGAAATTGTGCCA[C/T]AGACTCCAACCTGGG | 25853 |
rs55672700 | snp | A/G | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102723 | CCTGAATATACTGTT[A/G]GTGGCAAGCTAAAAT | 25853 |
rs55794917 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091199 | GGGCATGGTGGTACG[C/T]GCCTGTAGTCCCAGC | 25853 |
rs55812352 | in-del | -/AAAAC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110811 | AAAACAAAACAAAAC[-/AAAAC]CAAGAGTCTCCTCAG | 25853 |
rs55857848 | snp | C/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121512 | CAAGAACAGTCCCTG[C/G]TAGTCTTTGACTGGA | 25853 |
rs55914521 | snp | A/C/G | 0.320396 | 0.274693 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092427 | GTGCAGTGGCTCACG[A/C/G]CTGTAATCTCAGCAC | 25853 |
rs56012187 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104930 | CTCCAAAAAAAAAAA[-/A]GAAAGAATTTCACAA | 25853 |
rs56127807 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105934 | TTTGTACTTTTAGTA[G/T]AGACAGGGTTTCACC | 25853 |
rs56140730 | in-del | -/AAAGA | 0.375 | 0.216506 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088024 | TGAAGTAAGGGTGAG[-/AAAGA]CTATGTCATTTCAGC | 25853 |
rs56145814 | snp | A/T | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088953 | CATCTCTACTAAAAA[A/T]AAATAAATTAGCCGG | 25853 |
rs56157435 | snp | C/T | 0.429238 | 0.174281 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111105 | ATTCTCCTGCTTCAG[C/T]CCTCCGAGCAGCTGG | 25853 |
rs57158286 | in-del | -/TTTTTTTTT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095390 | TTTTTTTTTTTTTTT[-/TTTTTTTTT]GAGATAGGGTCTCGC | 25853 |
rs58312639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115048 | AGGGTGTTTCAGACT[A/G]GAGCCCAATGAGAAA | 25853 |
rs59340595 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108830 | TATATATATATATAT[-/AT]GAATGAGGTGGACAA | 25853 |
rs59375660 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121168 | CAAAAAACAAACAAA[A/C]AAACAAAAAAACCCA | 25853 |
rs60125831 | in-del | -/T | 0.479502 | 0.0991411 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095084 | TTGGACTTTGGAGGC[-/T]TTTTTTTTTGAGAGA | 25853 |
rs60261889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112664 | AGTACTTTGGGAGGC[C/T]GAGGAGGGCGGATCA | 25853 |
rs60279027 | snp | A/C | 0.391954 | 0.205789 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109880 | TGCAAAAGGTCTCGT[A/C]TGTGTTTTCTGTGAG | 25853 |
rs60507549 | in-del | -/AA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120687 | AAAAAAAAAAAAAAA[-/AA]GAAAACAAAGCAACC | 25853 |
rs61081369 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106112 | TAAGAAATTATTATT[A/C]TACAGGGTCACCCTC | 25853 |
rs61167233 | snp | C/G | 0.326035 | 0.238157 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109574 | GCAACAGCCACAGAG[C/G]GGGGTCCCACGCAGC | 25853 |
rs61292662 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121172 | AAACAAACAAACAAA[A/C]AAAAAAACCCAAGAA | 25853 |
rs61554557 | snp | G/T | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115191 | GAAATCAAAGCAGAA[G/T]AATCTATTCACTATC | 25853 |
rs61671999 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111281 | GAGCCACCGCACCCA[A/G]CCTCTCCTACTCTTT | 25853 |
rs61735450 | snp | C/G | 0.0422378 | 0.13905 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125260 | TTTCCTTTTGTGAAG[C/G]GAGTGATCCCAGCCA | 25853 |
rs61735452 | snp | A/C | 0.201446 | 0.24524 | missense | DCAF12 | GRCh38.p7 | 9:34098355 | AAGGCCAGAGCCCGA[A/C]CCTTGCAGTTGTCAG | 25853 |
rs62560864 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105058 | AGGAGTTTGAGACCA[C/G]CCTGGCCAATATGGT | 25853 |
rs62560866 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113154 | CTCCTGGGTACAAGC[A/G]ATTCTCCTGCCTCAG | 25853 |
rs66793833 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091340 | CAACAACAACAACAA[A/C]AAAAAAGAAATAGCT | 25853 |
rs68056708 | in-del | -/A | 0.337748 | 0.234095 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128418 | AAAGAAAAAAAAAAA[-/A]TTAGCTGGGCAACGT | 25853 |
rs71506165 | in-del | -/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088567 | GGCAGGAAAACGGGG[-/G]AGGAAGGGACAGGAA | 25853 |
rs71506166 | in-del | -/AACAA/AACAAAACAA/AACAAAACAAAACAA | 0.427879 | 0.260387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110783 | GCAAGACCCTGCCTC[lengthTooLong]AACAAAACAAAACAA | 25853 |
rs71506167 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120669 | GCAAGACGCGGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs71521213 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105202 | AGGTTGTGGTGAGCC[A/G/T]AGGTCGTGCTACTGC | 25853 |
rs71521214 | snp | A/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108810 | AAAAAAAAAAATAAA[A/T]AAATATATATATATA | 25853 |
rs71521215 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120035 | TGGTGAACCCTGTCT[C/T]TACTAAAAAACAAAA | 25853 |
rs71952947 | in-del | -/AT | 0.18989 | 0.242666 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108813 | AAAATAAATAAATAA[-/AT]ATATATATATATATA | 25853 |
rs72308374 | in-del | -/TA | 0.303688 | 0.244167 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108985 | TTATGTATATGTTTT[-/TA]TATATATATATATAT | 25853 |
rs72391664 | in-del | -/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119712 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCGTGC | 25853 |
rs72729401 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094009 | GTGCATACAACACAT[A/G]AGACAGCATACAAGG | 25853 |
rs72731203 | snp | A/T | 0.234109 | 0.249494 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098777 | TTATTTATTATTATT[A/T]TTTTTTTTTGAGACA | 25853 |
rs72731208 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105743 | TCTATCTATCTTATC[C/T]ATCTATCCATCCTTT | 25853 |
rs72731211 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106134 | GTCACCCTCTGTCAT[A/G]TAGGCTGGAGTGCAG | 25853 |
rs72731212 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109710 | GTGCAAGCGGGGGAA[C/T]AGGACCCTGTTCATG | 25853 |
rs72731214 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113019 | AATGCAACCATAACA[C/T]GTAGCTTTTAGACCA | 25853 |
rs72731216 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115066 | GCCCAATGAGAAAGG[A/G]AAGTAATTCTACGCA | 25853 |
rs72731217 | snp | C/T | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119555 | TACTTAAGTATTCGA[C/T]TGTTAGTATTTAGAT | 25853 |
rs72731218 | snp | A/C | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119678 | TTTAGGCTCTTCTTT[A/C]AACAAATACTATGTA | 25853 |
rs72731221 | snp | A/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122376 | CTTACTCTCTGCCAA[A/G]CTTCAACTAATTGAT | 25853 |
rs72731222 | snp | C/G | 0.104859 | 0.203554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122864 | TGTAGTTCTTTGCAG[C/G]CCCTACTACTCCTTA | 25853 |
rs72731224 | snp | C/T | 0.138207 | 0.223612 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122888 | CTCCTTACTGTCTTG[C/T]GCCTAGCAAACTTTT | 25853 |
rs72731225 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123794 | CTCTTCCAAGCAGGA[A/G]ACTCTTTTTCTACTC | 25853 |
rs73489344 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122115 | TCAGTATCAGTGGTT[C/T]TTAACCATTTTTGGC | 25853 |
rs73489346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123192 | GGACATTCTACATCA[A/T]AACTTTCCTATTGAG | 25853 |
rs73491038 | snp | C/T | 0.0376037 | 0.131863 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086026 | AACAAAAATTAATAT[C/T]CTATTCCCAGAGTAC | 25853 |
rs73491041 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088655 | ATTGGCTGGTTGGTT[C/T]TCATGGGAATCAGGG | 25853 |
rs73491042 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089352 | GTGGGGGCTGAGAGA[C/G/T]AGAGGAAGATAATTT | 25853 |
rs73491045 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092398 | ACAGGATAGAAAGTA[A/G]GGCTCTCGGCCAGGT | 25853 |
rs73491053 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097641 | GGGAAAGTAGGCAGT[A/G]AAGAATACTGGCCAG | 25853 |
rs73491056 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101333 | CTGCTTCAGTCTCTC[A/G]AAATACTGGGACTAC | 25853 |
rs73491058 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102211 | GGAGGGTCACTGGAG[C/G]CTGGAGAGGTCAAGG | 25853 |
rs73491065 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106155 | TGGAGTGCAGTGGCA[C/T]GATCACAGCTTGATG | 25853 |
rs73491069 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114453 | CAACCTCACCCTCAT[A/T]ATTGCAAAGGAATGA | 25853 |
rs74180533 | in-del | -/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088562 | GTCCCTTCCTCCCCC[-/G]TTTTCCTGCCCCATG | 25853 |
rs74190205 | in-del | AAAAATTAGCC/GAAATTAGCT | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115437 | TCTACTAAAAATACA[AAAAATTAGCC/GAAATTAGCT]GGGCGGCTGGGCACG | 25853 |
rs74206320 | multinucleotide-polymorphism | CGGTGGCTCACACCTGTAATCCCAGCACT/TGGTGGCCTGCACCTGTAGTCCCAGCTAC | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115461 | CCGGGCGGCTGGGCA[lengthTooLong]TTGGGAGGCTGAGGC | 25853 |
rs74326483 | in-del | -/AAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097952 | AAGAAAAAAAAAAAA[-/AAA]GGAATGAATACCAAA | 25853 |
rs74458889 | snp | C/G | 0.0182019 | 0.0936463 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086861 | GGACAACTGGGAGAA[C/G]AAGTTAAAAAACTGG | 25853 |
rs74523320 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097961 | AAAAAAAAAGGAATG[A/C]ATACCAAAGAGAAAA | 25853 |
rs74731669 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117156 | ACAGAATCATGACTT[C/T]GTGGAAGGAGGGCCA | 25853 |
rs75296201 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125948 | GGTTGGGTATACATA[C/T]AGGGAGACTACTTCC | 25853 |
rs75316284 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120235 | AAAAAAAAAAAAAAG[A/G]CCAGGTATGATGGCA | 25853 |
rs75463073 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100676 | ATTTTTGCATTTTTT[C/T]TTTTTTATAGACAGG | 25853 |
rs75759805 | snp | A/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111995 | CAAAAAAAAAAAAAT[A/T]AGCTGGATGTGGTGG | 25853 |
rs75781624 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100490 | GGAGTGAGACACCAC[A/G]CCCAGCTTCTTTTTT | 25853 |
rs76096442 | snp | A/G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097799 | TTAGCCATGTGTAGC[A/G/T]GTGCATGCCTGTAGT | 25853 |
rs76223147 | snp | G/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119719 | TTTTTTTTTTTTTTT[G/T]GAGACAGGGTCGTGC | 25853 |
rs76354427 | snp | A/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089133 | AAAAAAAAAAAAAAA[A/T]TCACTGACAGCTGTG | 25853 |
rs76470683 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120234 | AAAAAAAAAAAAAAA[A/G]GCCAGGTATGATGGC | 25853 |
rs76470825 | snp | A/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100671 | GGCTAATTTTTGCAT[A/T]TTTTTTTTTTTATAG | 25853 |
rs76502913 | snp | G/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119718 | TTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCGTG | 25853 |
rs76679743 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127603 | GGCCTCCAAACAAGG[A/G]GGCTTCATCAGGATC | 25853 |
rs76808469 | snp | C/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124592 | TTTAGATTCTGTTCA[C/G]TAAAAAACAGCCAAG | 25853 |
rs76839219 | snp | C/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086797 | ATTAAAAGGAGAATA[C/T]ATATATAATTTTTTT | 25853 |
rs76980262 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097800 | TAGCCATGTGTAGCG[G/T]TGCATGCCTGTAGTC | 25853 |
rs77082829 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094868 | ATGTAAGGAGCTATC[C/T]TGGGGATGGCACCCA | 25853 |
rs77130329 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115800 | ATGTTGTAATAAAAC[C/T]CACCTGGGCTCAGGC | 25853 |
rs77158465 | snp | C/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119956 | AAGTGATCTTCCTGT[C/T]TCAGCTTCCCAAAGT | 25853 |
rs77192126 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092706 | AAAAAACAACAACAA[A/C]AAAAAAAAAGTAGAG | 25853 |
rs77329227 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119305 | TTTATCAACAATACA[C/G]AAATTTAAAATGCAA | 25853 |
rs77539310 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110797 | TCAACAAAACAAAAC[A/C]AAACAAAACAAAACC | 25853 |
rs77642123 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105252 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 25853 |
rs77714624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100582 | TCATCCCAACCTCCA[C/T]CTCCTGAGCACAAGT | 25853 |
rs78041471 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097933 | AGCAAAACACAGTCT[A/C]AAAAAGAAAAAAAAA | 25853 |
rs78069542 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092707 | AAAAACAACAACAAC[A/C]AAAAAAAAGTAGAGC | 25853 |
rs78106753 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094966 | GCAATATTTTAAATA[A/G]TTTTCTGCATTAAAC | 25853 |
rs78634309 | snp | A/G | | | missense | DCAF12 | GRCh38.p7 | 9:34093442 | ATGGCAGTTTGGTGG[A/G]GAGGAGCTGAAAATA | 25853 |
rs78874271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111711 | TTTCAGGACAATCAG[A/T]CCAAAGGCTAGATTG | 25853 |
rs78972175 | snp | A/C | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120189 | GCCTGGGCAACAAGA[A/C]TGAAAGTCCGTCTCA | 25853 |
rs79101901 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110194 | GCCTAACTGGCATCA[C/T]TGCTGATGCATCCCA | 25853 |
rs79127312 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128027 | TCAGCTTTCTTTTTT[G/T]AGTCTGTTCTAATTC | 25853 |
rs79170046 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124110 | TAAACAGACACTTCT[C/G]CTAGTACTTAAGACT | 25853 |
rs79444484 | snp | A/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100681 | TGCATTTTTTTTTTT[A/T]TATAGACAGGGTTTT | 25853 |
rs79454236 | snp | G/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122493 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 25853 |
rs79611740 | snp | G/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119720 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCGTGCT | 25853 |
rs80030828 | snp | G/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117271 | ATTTTTTTTTTTTTT[G/T]AGATGGAGCTCAAAA | 25853 |
rs80314791 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125950 | TTGGGTATACATATA[G/T]GGAGACTACTTCCTT | 25853 |
rs111302055 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105252 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs111355052 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115314 | ATATGTATAGCGGCT[A/G]GGCGCGGTGGCTCAC | 25853 |
rs111577228 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093170 | CCCCTTTTTGAACAC[A/G]CTTCCAAATGTTCCA | 25853 |
rs111585246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117405 | TCTGCCTGCCTCGGC[C/T]GGCCAAAGTGCTGGC | 25853 |
rs111615835 | snp | A/G | 0.021333 | 0.101051 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113622 | TGGGATTACAAGCAT[A/G]AGCCACCGCACCAAG | 25853 |
rs111619198 | snp | A/G | 0.021333 | 0.101051 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118626 | AGAGACGGTAATTAC[A/G]TATCTGGTATAAGAG | 25853 |
rs111690330 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096711 | CAAAATCATGTTCAT[C/T]ACACCTTAGATAGTG | 25853 |
rs111818999 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116305 | CAGGCTGCAGAGATC[A/G]CGCCACTGAACTCCA | 25853 |
rs111822814 | snp | A/C | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091662 | AAAAAAAAAAAAAAA[A/C]CACAAAAAACCCAAA | 25853 |
rs111826695 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109840 | AGGGGTCGGAAGCAG[A/G]TGTCTTAGAGAGCTT | 25853 |
rs111953401 | in-del | -/AACAAC | 0.478271 | 0.101943 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102666 | ACAAACACACAAACA[-/AACAAC]AAACAACAACAAAAA | 25853 |
rs112014421 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115447 | ATACAAAAAATTAGC[C/T]GGGCGGCTGGGCATG | 25853 |
rs112100935 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089683 | CACTGAGTTTTCAAC[A/G]TCCACCCTGCTCCCC | 25853 |
rs112138431 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109908 | GAGCTGGTGGACGGA[C/G]AGGGTGACATTGTAG | 25853 |
rs112253611 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099089 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTCGCTCTA | 25853 |
rs112262010 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113964 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 25853 |
rs112374922 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126007 | GCTTCCTAGGGCCCA[C/T]GGAAGGTAGAGTTCA | 25853 |
rs112385098 | snp | A/G | 0.5 | 0 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086266 | GCCTCTAACCTGGAG[A/G]TAATGGCTTGTGTTC | 25853 |
rs112430605 | in-del | -/AAT | 0.0372196 | 0.131242 | cds-indel | DCAF12 | GRCh38.p7 | 9:34088099 | ATAGGGATTAGCAAC[-/AAT]GTTTGGTTGAAAAGC | 25853 |
rs112581999 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092709 | AAACAACAACAACAA[A/C]AAAAAAGTAGAGCTT | 25853 |
rs112583372 | snp | A/C | 0.0520825 | 0.152737 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127904 | TCTCCTGCCATCCCA[A/C]GTCGGCACTACCACT | 25853 |
rs112632354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089245 | TTTTCCCACAGGCAA[C/T]GTGCAGACATAAAAG | 25853 |
rs112680649 | in-del | -/T | 0.411242 | 0.191052 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105755 | TCTATCTATCCATCC[-/T]TTTTTTTTTTTTTGA | 25853 |
rs112718526 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095508 | GCCTCAGCACTGCTA[C/G]CCTCCAGTAGCTGGG | 25853 |
rs112730142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092233 | CATATGTATATATCC[A/G]TGACATCATAACCAC | 25853 |
rs112759678 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125955 | TATACATATAGGGAG[A/G]CTACTTCCTTCTTCC | 25853 |
rs112775414 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096544 | AGGAGGCAGAGGTTG[C/T]AGTGAGCCAAGATTG | 25853 |
rs112813628 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115357 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 25853 |
rs112858759 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100476 | GTGCTGGGATTACAG[A/G]AGTGAGACACCACGC | 25853 |
rs112951018 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112961 | CAAATTATTTCCTGA[A/C]ACAAAATTAATTGCC | 25853 |
rs113192832 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104558 | ACTGTGTTTCAGAAG[A/T]TTACTTTGTGTACAG | 25853 |
rs113225365 | snp | A/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115375 | GGCGGGCGGATCACG[A/T]GGTCAGGAGATCGAG | 25853 |
rs113347704 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094584 | CGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 25853 |
rs113354924 | in-del | -/T | 0 | 0 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126790 | ACCGCCGGAACGAGA[-/T]GGGCGGGATCTAGGG | 25853 |
rs113491051 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115318 | GTATAGCGGCTAGGC[A/G]CGGTGGCTCACACCT | 25853 |
rs113515434 | snp | C/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111932 | TTCAAGTCAGGAGTT[C/T]AAGACTAGCCTGGCA | 25853 |
rs113572373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125705 | CAGACCTGGCTCCCA[A/G]GTCTTCCAGGGATGC | 25853 |
rs113601725 | snp | A/G | 0.000230819 | 0.0107404 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088434 | CGTTCCAGACGAGTC[A/G]TAGCAGTGGGTGTAA | 25853 |
rs113664484 | snp | C/T | 0.5 | 0 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34096725 | TCACACCTTAGATAG[C/T]GTATTTTCAGCCTTC | 25853 |
rs113819662 | snp | A/G | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115472 | GGCATGGTGGCCTGC[A/G]CCTGTAGTCCCAGCT | 25853 |
rs113824929 | in-del | -/T/TT | 0.5 | 0 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128255 | TCGCGATTTCTTTTC[-/T/TT]TTTTTTTTTTTTTGA | 25853 |
rs114013473 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089737 | GACAGTGTTTTCCCA[A/C]TGGCAAGTTAGCTCA | 25853 |
rs114035868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115133 | AGTAAAAGACAGGTG[A/G]GCAACCTAAGTCTGT | 25853 |
rs114179064 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114163 | TTTAGCTATAAAAAA[A/G]AATGAAATCCTTTGG | 25853 |
rs114256136 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117598 | TAGCTACCTTAAGCA[C/T]CTATCTAAACAAATA | 25853 |
rs114436823 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107060 | CTGTTCACTGCTATG[C/T]CTCAAACAACGCCTA | 25853 |
rs114689532 | snp | A/G | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120044 | CTGTCTCTACTAAAA[A/G]ACAAAAAAATTAGCC | 25853 |
rs114703852 | snp | A/T | 0.0146672 | 0.084371 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127844 | GTCAACAAGGAGATT[A/T]GGATTTGTTTTCCAA | 25853 |
rs114707756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092762 | TAACTAATATCCTGA[C/T]TGGTGGCTCCCAACA | 25853 |
rs114966849 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098128 | ACTCAGAGAAATACT[A/G]CAGACACCAATTGAA | 25853 |
rs115277969 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117446 | TGAGCCACCGCGCCC[A/G]GCCTCTAATCCTTGA | 25853 |
rs115285410 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092339 | GCCACATCTTAGCAT[A/G]AATAGAATTTTAGTT | 25853 |
rs115405158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103902 | CTTTTTCCAGTAAAC[C/T]TATTTGCCAGTTCTC | 25853 |
rs115445413 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088660 | CTGGTTGGTTCTCAT[A/G]GGAATCAGGGCCTCA | 25853 |
rs115473790 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109893 | GTCTGTGTTTTCTGT[A/G]AGCTGGTGGACGGAG | 25853 |
rs115554410 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106976 | TATTAGTTTATATGG[C/T]TTATGTTTTGTCTAT | 25853 |
rs115748306 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122817 | CTCAAATTCCTACAC[A/G]GCAACAGTTGGTTAA | 25853 |
rs115966352 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105515 | GCTGGGTGTGAAGGT[A/G]TGTGCCTATAGTCCC | 25853 |
rs116273425 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101368 | GTAAGCCACTGTGCC[C/T]GGCCATAATTCCTTT | 25853 |
rs116413480 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101131 | AGCTGGAGTGCAATA[A/C]CATGATTATGGCTCA | 25853 |
rs116414716 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092222 | TGAGGTTCTGACATA[C/T]GTATATATCCATGAC | 25853 |
rs116497065 | snp | A/G | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105312 | GCCTGTATAATCTAA[A/G]CACTTTGGGAGGCTG | 25853 |
rs116863861 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121031 | TGGTGGCATGTGCCC[A/G]TACTCCCAGCCACTC | 25853 |
rs116885684 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096849 | CGATAATAAGCAGGC[A/G]AGGATTCTAAGGTCA | 25853 |
rs116939720 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094130 | AGAGAAAAAGCTGGG[C/G]GTGGTGGCTAACGTC | 25853 |
rs117005636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099545 | CTCGAAATTCTTTAA[C/T]GAGAATTTTATACAT | 25853 |
rs117094918 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116928 | AGGTTGCAGTAAGCC[A/G]AGATCGTGCCCCTAC | 25853 |
rs117274212 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105530 | GTGTGCCTATAGTCC[C/T]AGCTACCTGGGAGCC | 25853 |
rs117317727 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086762 | GACTTGCTGTCTCTC[C/T]TCTCCAGTAGCCCCC | 25853 |
rs117474949 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124137 | GACTTTCTTGATCTA[C/G]AGCAATCTTCTCTCT | 25853 |
rs117490135 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105564 | GGCAGAAGGATCACT[A/T]GAGCCCAAGAGCTCA | 25853 |
rs117622511 | snp | C/T | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098871 | TCTCCTGGGTTCAAG[C/T]GATTCCCGTGCCTCA | 25853 |
rs117914026 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097887 | GCTTTGAGCTGAGAT[C/T]GTGCCATTGCACTCC | 25853 |
rs117997985 | snp | C/T | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113176 | CTGCCTCAGCCTCGC[C/T]GAGTACCTGGGATTA | 25853 |
rs118034221 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126001 | ATCCCAGCTTCCTAG[A/G]GCCCATGGAAGGTAG | 25853 |
rs118133690 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124254 | AACCGAGGGAGGGCT[C/G]GGCGTAATCATTTCC | 25853 |
rs137881768 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111090 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGCTTCAGC | 25853 |
rs137919024 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101688 | TGAGCCACTGTGCCC[A/G]GCCCACAATCCTTCT | 25853 |
rs137967423 | snp | A/G/T | 0.000249501 | 0.0111665 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096784 | CTGCTCCCAGTTCCT[A/G/T]CAAGAGCAATGAAAA | 25853 |
rs138064420 | snp | A/G | 0.333722 | 0.235565 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093101 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 25853 |
rs138097919 | in-del | -/ATATATA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110041 | TTTATATATTTAAAT[-/ATATATA]ATATATGTTTATTAA | 25853 |
rs138217138 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092862 | ACACCCCTTTTTTTT[-/T]GAGACAGAATTTCGC | 25853 |
rs138263708 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115189 | GTGAAATCAAAGCAG[A/C]AGAATCTATTCACTA | 25853 |
rs138275854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089877 | TTGGCCGAAGACCAT[A/G]AGTGCTGAGAACTTC | 25853 |
rs138423361 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091422 | GAGGCTGAGGTGGGT[G/T]TCCCAAGAGTTTGAG | 25853 |
rs138491397 | snp | A/G | 0.000296467 | 0.0121715 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107428 | GGGGTTGTCTCCTCC[A/G]GTGGCTAGCAGTGTT | 25853 |
rs138517549 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106043 | GTGAGCCACCACACC[C/T]GGCCTATATTTTAAA | 25853 |
rs138557819 | snp | A/G | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105810 | CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 25853 |
rs138695651 | in-del | -/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117934 | AAACAAACAAAAAAA[-/G]AAATTATTCTTGGAC | 25853 |
rs138819167 | snp | G/T | 0.00021417 | 0.010346 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125205 | TGACTTCCCGGTTCT[G/T]CAAGTAGTATACTAA | 25853 |
rs138849381 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118389 | TCCACCTGCCTCAGC[C/T]TCCCAAAGTGCCGGG | 25853 |
rs138979558 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111591 | TTTCAGAGGGCCTGC[A/C]CAACTACTGTAGTAG | 25853 |
rs139034747 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120614 | GGCAAAGGTTACAGT[A/G]AGCCAAGATCGTGCC | 25853 |
rs139077086 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092041 | GTACACTAAAATAAG[C/T]ATTTTTTCCCTCTTC | 25853 |
rs139188279 | in-del | -/TATA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108985 | TTATGTATATGTTTT[-/TATA]TATATATATATATAT | 25853 |
rs139198427 | snp | A/C/T | 9.89065e-05 | 0.00703172 | missense | DCAF12 | GRCh38.p7 | 9:34089516 | ATCTCTGAGCTCGGA[A/C/T]GTCATAGAACAGCAG | 25853 |
rs139307764 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108352 | ATATCTGCCCTAATA[C/G]ATACACCTTATAGCC | 25853 |
rs139424801 | in-del | -/T | 0.231189 | 0.249291 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099592 | ATTTTTCTTTTTTTT[-/T]CCCTTTTTTTGGAGA | 25853 |
rs139628228 | snp | A/G | 0.325799 | 0.238232 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112685 | GGGCGGATCATCTGA[A/G]GTTGGGAGTTCGAGA | 25853 |
rs139741935 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087520 | CACCTGGATGGTGAG[A/T]CTGATGTTTTAGGGG | 25853 |
rs139769951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119284 | TGTTTATTGTACAAA[C/T]GATACTTTATCAACA | 25853 |
rs139828879 | snp | A/C | 0.00194363 | 0.0311133 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127224 | ACCAACCCAGGCCGC[A/C]CTACGAGTCTCTGGC | 25853 |
rs139868448 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088431 | TTTCGTTCCAGACGA[A/G]TCGTAGCAGTGGGTG | 25853 |
rs139959028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097875 | AAGGTGGAGGTTGCT[C/T]TGAGCTGAGATCGTG | 25853 |
rs140014797 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115413 | TGGCTAACATGGTGA[A/G]ACCCCGTCTCTACTA | 25853 |
rs140020039 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112486 | GTAATCCTGGCTACT[C/T]GGGAGGCTGAGGCAG | 25853 |
rs140039233 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109191 | CCACCTCCTCATAGG[A/C]CCACTCCTCAAACTC | 25853 |
rs140076757 | snp | A/C/G | 0.000560195 | 0.0167283 | missense | DCAF12 | GRCh38.p7 | 9:34098454 | GACACATTGTGTCTC[A/C/G]CATCACTTTTGGTCA | 25853 |
rs140196001 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102576 | GAGAATTGCTTGAAC[C/T]CAGGAGACGGAGGTT | 25853 |
rs140215009 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110399 | TACAGCTGACTCCTT[C/T]CTCTGCTTCCTCACT | 25853 |
rs140339092 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100620 | TCACCTCAGCCTCCT[A/G]AGTAGCTGTGACTAC | 25853 |
rs140370649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120334 | GCAGTGAGCCATGAC[C/T]GCACCACTGTACTCC | 25853 |
rs140412096 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116342 | GCGACAGAGAGAGTC[C/T]GTCTCAAAAATAAAT | 25853 |
rs140413293 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105018 | GCCAATTTTGGGAGG[A/C]CGAGGCAGGCGAATC | 25853 |
rs140458755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100355 | AGAGGCCCGTCACCA[C/T]GCCTGGCTAATTTTT | 25853 |
rs140591380 | snp | C/T | 4.04408e-05 | 0.00449653 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106494 | AGTCCTTGTGTCCAT[C/T]CTTGGAGAGCAGGGA | 25853 |
rs140616224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114726 | GGGGGAAAGAGACAT[A/G]TAAGACTAGTGAGTC | 25853 |
rs140681303 | snp | A/C | 0.391583 | 0.206044 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121725 | CAAGGCAGGCGGATC[A/C]CGAGGTCAGAAGATC | 25853 |
rs140753954 | snp | G/T | 6.58924e-05 | 0.0057395 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107486 | ATACCACAGCCCTGC[G/T]GGGTCACACCTCCAG | 25853 |
rs140785234 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103576 | ATTATGTTTTAGGCC[A/G]GGCATAGTGGCTCAT | 25853 |
rs141173289 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102370 | ACAATAATAAAGCAC[G/T]TAAAAACCCAGGCCG | 25853 |
rs141324661 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116090 | AATCCAGGGCTGGGT[A/G]CGGTGGCTCACGCCT | 25853 |
rs141325556 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118295 | TGCGGCATCATGCCC[A/G]GCTAATTTTTGTGTT | 25853 |
rs141445025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121141 | CCTGAGCAACAGAGC[A/G]AGACTCCATCTCAAA | 25853 |
rs141543913 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106880 | TTCTGATACAGCATC[C/T]TCCACCTTACTCTCA | 25853 |
rs141617386 | in-del | -/A | 0.425894 | 0.177655 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102015 | GTGAGACCCTGTCGC[-/A]AAAAAAAAAAAAAGA | 25853 |
rs141689215 | snp | A/G | 0.000439657 | 0.0148201 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125159 | GCATAACCATGCAAC[A/G]CTCGAGAGTAGCTGG | 25853 |
rs141742042 | in-del | -/AGG | 0.000170593 | 0.00923404 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098528 | TGAGCCTGCAGGGCC[-/AGG]AGAACACAGATGTCA | 25853 |
rs141780851 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092922 | GCGATCTCAGCTCAC[C/T]GCAACCTCCGCCTCC | 25853 |
rs141814520 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123651 | TTAAATTATTACTTA[A/C/T]TATGCTCGCCTTCAA | 25853 |
rs141836775 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102363 | TTAGCAAACAATAAT[-/A]AAGCACTTAAAAACC | 25853 |
rs141918518 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115650 | CTATAGTCTCTGCAG[A/T]CTCCCCATAGACATA | 25853 |
rs141991771 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111433 | CACAACACTTAGACC[A/G]TATCGCACTGATTTA | 25853 |
rs142106950 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120507 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAT | 25853 |
rs142253533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099523 | AGGCATGAGCCACCG[C/T]GCCTTACTCGAAATT | 25853 |
rs142299954 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097670 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGA | 25853 |
rs142342072 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093017 | CGCCCGGCTAATTTT[G/T]TATTTTTAGTAGAGA | 25853 |
rs142344955 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100812 | GCCTTATTTTTTTAA[-/T]TTTTTTTTGTAGAGA | 25853 |
rs142367246 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090018 | CATTAAGTCATCAAC[A/G]ATTCCTTATATTTCA | 25853 |
rs142386109 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092660 | CACTACACTCCAGCC[G/T]GGCAAAAGAGCGAGA | 25853 |
rs142493413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126048 | GTTTGTTTCCGATTC[C/T]CTTAACTTCGGTTTC | 25853 |
rs142673522 | in-del | -/ATATA | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110043 | TATATATTTAAATAT[-/ATATA]ATATATGTTTATTAA | 25853 |
rs142835990 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112325 | CCCAGGCTGAGCGTG[A/G]TGGTTCACGCCTGTA | 25853 |
rs142842344 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104159 | AGTCCCAGCTACTTG[A/G]GAGGCCGAGGCAAGA | 25853 |
rs142999280 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115302 | CAAACATTAAAAATA[A/T]GTATAGCGGCTAGGC | 25853 |
rs143094429 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102179 | CTGTGGTACCAGCTA[C/T]CCGGGAGGCTGAGGT | 25853 |
rs143120526 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087184 | AGTAGGAGGGGTGGC[G/T]TCAACCCCAAGTCCC | 25853 |
rs143135409 | in-del | -/AAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118974 | TGTCTCAAAAAAGAA[-/AAT]AATAATAATAATAAT | 25853 |
rs143586017 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119870 | CCATGCCCAGCTAAT[G/T]CTTAAATATTTTGTA | 25853 |
rs143639670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112516 | GGAGAATTGCTTGGA[C/T]CCAGGAGGTGGAGGT | 25853 |
rs143751612 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124362 | ACGTTTCTGCTCTTT[A/G]ACTTATTTTATCCTG | 25853 |
rs143814490 | snp | A/G | 0.230896 | 0.249269 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116911 | TTGAACCCAAGAGGC[A/G]GAGGTTGCAGTAAGC | 25853 |
rs143952809 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103278 | CCGGCGTGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 25853 |
rs144010083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092256 | ATAACCACAATCTAC[A/G]TAATGAACATACTCA | 25853 |
rs144118073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106064 | ATATTTTAAAATTTT[C/T]TTACAATAAATGTGT | 25853 |
rs144141231 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109415 | AGCCATCTTTAGCCC[C/G]CAGGGTGGGATGTTA | 25853 |
rs144163718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116580 | CTTGGGAGGCTGAAG[C/T]AGGAGAATCGCCTGA | 25853 |
rs144311764 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099601 | ATTTTTCTTTTTTTT[C/T]CCTTTTTTTGGAGAT | 25853 |
rs144471394 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125504 | AATTACAAGGGCTGA[A/C]AGTCAAGGGAATGAA | 25853 |
rs144482947 | snp | A/G | 0.0271762 | 0.113356 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087535 | TCTGATGTTTTAGGG[A/G]TGTGGCTACTGGCTA | 25853 |
rs144602632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119282 | AGTGTTTATTGTACA[A/T]ACGATACTTTATCAA | 25853 |
rs144669491 | snp | A/G | 0.000148245 | 0.00860815 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34093350 | CCGTGGATCCAAGAA[A/G]GAGACATGAGCTTGG | 25853 |
rs144688180 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115718 | CTGAGGAACTAGTGA[G/T]GGGTGAACAGTTTGA | 25853 |
rs144790428 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112036 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGACAGG | 25853 |
rs144859902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098149 | ACCAATTGAAGGGGT[A/G]GGTTTCAGAGCCTCA | 25853 |
rs145095551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121307 | TAAGATACCCAAACA[C/T]AGAATTTGCCCGTCG | 25853 |
rs145111500 | snp | A/C | 0.333952 | 0.235483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113874 | AGCACTTTGGGAGGC[A/C]AAGGCAGGCGGATCA | 25853 |
rs145115184 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118322 | TGTTTTTAGTAGAGA[C/T]GGGATTTCATCATGT | 25853 |
rs145366410 | snp | C/T | 0.000115339 | 0.00759318 | missense | DCAF12 | GRCh38.p7 | 9:34093420 | AGACACACATTCTCA[C/T]GGCAATATGGCAGTT | 25853 |
rs145472399 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116806 | GCCAACATGGCGAAA[C/T]GCCATCTCTACTAAA | 25853 |
rs145575390 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113214 | CTGCCACCACGCCCG[C/G]CTAATTTTTGTATTT | 25853 |
rs145607255 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099099 | TTGAGACAGAGTCTC[A/G]CTCTATCACCCAGGC | 25853 |
rs145740652 | snp | C/T | 0.000441918 | 0.0148581 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089639 | GGAGAGAATATTTGC[C/T]GACTGTCTGCTAGCC | 25853 |
rs145778072 | snp | A/G | 0.00716266 | 0.059414 | | | GRCh38.p7 | 9:34103929 | TCTCCTTTGAGACCA[A/G]GAAGGTGCCCTTCCC | 25853 |
rs145946538 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126058 | GATTCCCTTAACTTC[C/G]GTTTCCCCTTCCTCC | 25853 |
rs146066747 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108882 | CAACTACTTAGCTAC[G/T]CAGGAGGCTGAGGCA | 25853 |
rs146090723 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115321 | TAGCGGCTAGGCGCG[A/G]TGGCTCACACCTGTA | 25853 |
rs146118060 | in-del | -/GA | 0.0368353 | 0.130617 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101780 | GCAACTTGGGAGGCT[-/GA]GAGGTAGGTGGACCG | 25853 |
rs146210554 | snp | C/T | 0.031825 | 0.122064 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095199 | CCTGCCTCAGCCTCC[C/T]AAGTATCTGGGACTA | 25853 |
rs146221846 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091527 | TATAGTCCCAGCTAC[C/T]CGGGAGGCTGAGGTG | 25853 |
rs146296271 | in-del | -/AAAC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124750 | AAAAATATGAGGCAA[-/AAAC]AAACAAACAAACAAA | 25853 |
rs146423723 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088943 | GGCGAGACCCCATCT[C/T]TACTAAAAAAAAATA | 25853 |
rs146529860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109615 | TTGGCATCAAACATC[C/T]GCTGGATGGGCTTGG | 25853 |
rs146624633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121015 | GAAAATTAGCTGTGC[A/G]TGGTGGCATGTGCCC | 25853 |
rs146669230 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087324 | AAAACCCACTGGGGA[G/T]ATTGGAAGAATGGCA | 25853 |
rs146758921 | in-del | -/TG | 0.00358779 | 0.0422022 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088064 | CCAGAGACAGGAGAA[-/TG]TGTGTCACTTAAAGA | 25853 |
rs146841130 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121422 | TTCCAGCACTCTTAC[C/T]GAGAGGTCCCTCGCT | 25853 |
rs146900837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111583 | CAGTCACCTTTCAGA[C/G]GGCCTGCCCAACTAC | 25853 |
rs146934053 | snp | C/T | 0.105214 | 0.203807 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106033 | GATTACAGGTGTGAG[C/T]CACCACACCCGGCCT | 25853 |
rs147028958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089875 | TTTTGGCCGAAGACC[A/G]TAAGTGCTGAGAACT | 25853 |
rs147196403 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120135 | TTCAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 25853 |
rs147226171 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124479 | GCTACTTTCCAAAGA[A/G]CTAATGCTTATACCC | 25853 |
rs147302707 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103492 | CCCATACACAAAGTT[A/G]TTTATTCGGAACACT | 25853 |
rs147332697 | snp | A/G | 0.00164562 | 0.0286374 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106453 | CACTGCCATAGTGTC[A/G]CTGATCCATGCGATG | 25853 |
rs147398556 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104774 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGGGC | 25853 |
rs147483332 | in-del | -/TTTCT | 0.329084 | 0.237162 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128247 | TAGCAGAGCTCGCGA[-/TTTCT]TTTCTTTTTTTTTTT | 25853 |
rs147681004 | snp | A/G | 0.000513615 | 0.016017 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34096752 | CTTCCAGAGATGAAA[A/G]TAGCCATCCAGAGAC | 25853 |
rs147681728 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099212 | AGCTGAGATCACAGG[C/T]GCATGCTACCATGCC | 25853 |
rs148043008 | snp | G/T | 6.59185e-05 | 0.00574064 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125238 | ATCTCTTCACAGGAG[G/T]AAGTCTTTTCCTTTT | 25853 |
rs148073251 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090387 | GTCTTTATCTAGTAT[C/T]AGGTGTTTTGAGAGT | 25853 |
rs148104182 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112281 | TCCAATAAATGTGAG[C/T]GGGTTTCTTATCCTT | 25853 |
rs148123227 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102284 | CTCCAAAAAAAAAAA[-/A]GAATAATGACTGTTT | 25853 |
rs148148525 | in-del | -/A | 0.117886 | 0.21224 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117282 | TTTGAGATGGAGCTC[-/A]AAAAAAAAAAGGTGC | 25853 |
rs148189620 | snp | A/G | 0.030278 | 0.119257 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102182 | TGGTACCAGCTACCC[A/G]GGAGGCTGAGGTGGG | 25853 |
rs148227352 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109005 | ATATATATATATATG[G/T]TTTTTTTTTTTTTCA | 25853 |
rs148240136 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094832 | ACCGCACCCGGCCCC[A/G]ATTTTTAAATATCTA | 25853 |
rs148365845 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114690 | GAGGCTCGGGCTCCC[C/T]GCAGTTTACATTCTA | 25853 |
rs148431891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125762 | CATGCCCGCGCTCCA[A/G]GCAGTTGCAGAATTC | 25853 |
rs148505403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103933 | CTTTGAGACCAAGAA[A/G]GTGCCCTTCCCACAC | 25853 |
rs148638383 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086800 | AAAAGGAGAATATAT[A/G]TATAATTTTTTTTCC | 25853 |
rs148683837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115875 | AGCCATCAAGCCTTG[C/T]CACTACATACCTTTA | 25853 |
rs148765621 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106599 | GTCAGACTGAAAATA[C/T]TTTTGTAGAAATTAC | 25853 |
rs148833546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116838 | ATACATAAATTAGCC[A/G]GGCACAGTGACGGGT | 25853 |
rs149085565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109692 | GAGTCCAGACATGAA[G/T]AAGTGCAAGCGGGGG | 25853 |
rs149115505 | snp | A/G | 0.00435613 | 0.046466 | missense | DCAF12 | GRCh38.p7 | 9:34093402 | CATTCACTACCATAA[A/G]CCAGACACACATTCT | 25853 |
rs149310028 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34125383 | TACTGCAGAATTTAC[A/G]AACAACACAAATACA | 25853 |
rs149390215 | snp | A/C | 0.39979 | 0.200158 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092694 | TGTCTCAAAAAAAAA[A/C]AACAACAACAACAAA | 25853 |
rs149489909 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102065 | AGGCTGGGTACAGTG[A/G]TATATGCCTTTAATC | 25853 |
rs149572349 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119182 | ACTACTGTATTTTTG[A/G]GCCCCTACTTCGGTC | 25853 |
rs149710701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112755 | AATACAAAATTAGCC[A/G]GGTGTGGTGGCACAT | 25853 |
rs149791869 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103895 | TAAAATTCTTTTTCC[A/G]GTAAACTTATTTGCC | 25853 |
rs149837222 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089267 | ACATAAAAGCAAAAT[C/T]GGGGGAAGTCTTTTC | 25853 |
rs149845915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098108 | CTGACCCACAAATAT[A/G]GACTACTCAGAGAAA | 25853 |
rs149879408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120941 | GGTGGATCACCTGAG[C/G]TCAGGAGTTCGAGAC | 25853 |
rs149964872 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34093320 | ACAGACAGACTTGAC[A/G]TTGTATGATGGCTGC | 25853 |
rs149972662 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108517 | ATAAAAAGGGCCGAG[A/C]GCAGTGGCTCACGCC | 25853 |
rs150112523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105735 | CTTTTTTATCTATCT[A/G]TCTTATCTATCTATC | 25853 |
rs150195321 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123770 | TGCACGTGCGGGGAG[A/T]GGAATGAACTCTTCC | 25853 |
rs150230899 | in-del | -/AAAGA | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088020 | AGAGTGAAGTAAGGG[-/AAAGA]TGAGCTATGTCATTT | 25853 |
rs150436123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118896 | CTTGAACCTGGGAGG[C/T]GGAGATTGCAGTGAG | 25853 |
rs150474359 | snp | C/G/T | 1.64732e-05 | 0.0028699 | splice-donor-variant | DCAF12 | GRCh38.p7 | 9:34107358 | TACTGGGAAAACTTA[C/G/T]ATCTCCTACACACAC | 25853 |
rs150490667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114749 | AGTGAGTCTATCTCT[A/G]CATGCATTCATGTGT | 25853 |
rs150514199 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097798 | ATTAGCCATGTGTAG[C/T]GGTGCATGCCTGTAG | 25853 |
rs150564298 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091419 | TGGGAGGCTGAGGTG[G/T]GTGTCCCAAGAGTTT | 25853 |
rs150654337 | in-del | -/ATTT | 0.0599851 | 0.162463 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118118 | AGAAGATGGAAATTG[-/ATTT]ATTTCTTTTGTTTTT | 25853 |
rs150782676 | snp | C/G | 0.000153988 | 0.00877328 | missense | DCAF12 | GRCh38.p7 | 9:34089461 | TCCCCTGCTAGTCTG[C/G]GCTTGGACCCATAAC | 25853 |
rs150804130 | snp | C/T | 0.230603 | 0.249246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099313 | GCAATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 25853 |
rs150806722 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116217 | TAAAAATTAGCCGGG[C/T]ATGGTGGCAGTCGCC | 25853 |
rs150850362 | snp | C/T | 3.29652e-05 | 0.00405974 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107328 | TTTAAAAACAAGGCT[C/T]CCTCCAACTACAACT | 25853 |
rs150904705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102477 | ACCGACCTGACCAAC[A/G]TGGTGAAACCCTGTC | 25853 |
rs151125517 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088803 | GCACAGGAGGAAGAA[A/C/T]CAAACACTTGAATAA | 25853 |
rs151129137 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116966 | CCTGGGCAATAGCGC[A/G]AGACTCCGTCTCAAA | 25853 |
rs151159187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110155 | CTCTCAAACTGGCAA[C/T]TACCTGAGAGCAGCA | 25853 |
rs151180447 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120539 | GGCCAGGCATGGTAG[C/T]ACGCGCCTGTAGTCC | 25853 |
rs151311642 | snp | A/C | 0.000282065 | 0.0118724 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106492 | CCAGTCCTTGTGTCC[A/C]TCCTTGGAGAGCAGG | 25853 |
rs180696117 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125592 | GAAATGAGAGGTAGA[C/G]TGATTCCCATACCGA | 25853 |
rs180741662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104354 | AGGCCACAGAGACAA[C/G]GGCACATCTGGAGAA | 25853 |
rs180742885 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115730 | TGATGGGTGAACAGT[C/T]TGAACTACTGTACAT | 25853 |
rs180759208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095933 | GAGCCTCTCAGGAAG[C/T]TTATGCAATAGGAAA | 25853 |
rs180880265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119243 | GCAAGGTTCATCTAG[C/T]TGAAATAACAGTTTT | 25853 |
rs180884613 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092642 | AGTGAGCTGAGATCA[C/G/T]GCCACTACACTCCAG | 25853 |
rs180997848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110356 | TTCCATCATCCTAGT[C/T]CTGCCTAACCTACCT | 25853 |
rs181101194 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095600 | TACTGTGTTGCCCAG[G/T]CTAGTTTTGAACTCC | 25853 |
rs181108393 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115452 | AAAAATTAGCCGGGC[A/G]GCTGGGCATGGTGGC | 25853 |
rs181209541 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104855 | CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 25853 |
rs181289477 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126890 | TGGATGGAAGTGGAC[A/G]AGCTGGGGCCAAGGG | 25853 |
rs181438029 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120349 | TGCACCACTGTACTC[C/T]ACCCTGAGTGCAAAA | 25853 |
rs181518066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101564 | TGCCCGGCTAATTTT[G/T]TATTTTTAGTAGAGA | 25853 |
rs181529131 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090527 | TGGGATATGAAGATG[G/T]CTCTTGGCACATAAG | 25853 |
rs181634528 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104410 | TTATGGGGTGCAAGC[A/C]TGGAAGCTATGAGAG | 25853 |
rs181673995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109886 | AGGTCTCGTCTGTGT[C/T]TTCTGTGAGCTGGTG | 25853 |
rs181713779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126200 | CCCTCCAGTTAACGA[G/T]GGTCCAGTCCTGACC | 25853 |
rs181915657 | snp | A/C | 0.000192444 | 0.00980739 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089603 | TTCCTGAAAGACAGA[A/C]AAGTAAAAGGCAGTG | 25853 |
rs182009926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100635 | GAGTAGCTGTGACTA[C/T]AGGCACACCCTACCA | 25853 |
rs182117524 | snp | A/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086579 | AAGTTCTGTGAGAAC[A/T]AAGAAATCTACAGCC | 25853 |
rs182176641 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121637 | AATCACACCCCACCC[C/G]CAGCCCCTTCAAGAG | 25853 |
rs182306834 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119698 | AATACTATGTACTTT[C/G/T]GCGGTTTTTTTTTTT | 25853 |
rs182366784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098820 | GTCACCCAGGCTGGA[A/G]TGCAGTGGTGCGATC | 25853 |
rs182456569 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127667 | AATATGACTGCCAGC[A/C]TTCGCTTTCCTCAAG | 25853 |
rs182479449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093899 | TGAATGGGAATTGTA[C/T]GCTATAGAAAGCACG | 25853 |
rs182492239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114041 | TGAACCTGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 25853 |
rs182622982 | snp | G/T | 0.000691916 | 0.0185871 | missense | DCAF12 | GRCh38.p7 | 9:34098372 | CTTGCAGTTGTCAGG[G/T]TTTGTGTCTTCTTTG | 25853 |
rs182638027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118342 | TTTCATCATGTTGGC[C/T]GGGCTGGTCTCGAAC | 25853 |
rs182721001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117391 | TCCTCACCTCGTGAT[C/G]TGCCTGCCTCGGCCG | 25853 |
rs182753675 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121207 | GACTAAACCACAAAA[A/C]GATCAAACATCCCCT | 25853 |
rs182975118 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128186 | CTTTCTCAAAGTTCC[G/T]TTACTTCATCTTCAC | 25853 |
rs183022125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102400 | GGGCACGGTGGCTCA[C/T]GCCTGTAACCCCAGA | 25853 |
rs183039612 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087363 | TCTCCTCAAAGCCAT[A/G]GGGGCTATGGATGTG | 25853 |
rs183048482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107746 | CATGAAATAAGTCAA[C/T]ATAACACAATATTAG | 25853 |
rs183177314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093034 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATATT | 25853 |
rs183182665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111252 | GCCTCCCAAAGTGCC[A/G]GCATTACAGGTGTGA | 25853 |
rs183235485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093216 | CTGTTTGGAAACCAA[C/T]AAAGAAACTGAAAGT | 25853 |
rs183325887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102893 | CCAGCCTGGGCAAAA[C/T]GTTGAAACACCATCA | 25853 |
rs183479704 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112388 | ATCACCTGGGGTCAG[A/G]ACTTCAAGACCAGCC | 25853 |
rs183609068 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116535 | CAAAAATTAGCCGGG[C/T]ATAGTAGTGCGTACC | 25853 |
rs183634267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088834 | TTCACTGGAGGTGGG[A/G]CGCAGTGGTTCATGG | 25853 |
rs183648087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108318 | AGTGTTATGAACACA[C/G]CTATGAACGAGAGAA | 25853 |
rs183819703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096885 | CTTTATTCCTGTCTC[A/G]TGATGATTCCAGCAG | 25853 |
rs184061996 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099947 | GGCATGCATCCACAG[C/T]TGACTTTTAGTGGGC | 25853 |
rs184069148 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119014 | TTATCTCACACTTAC[G/T]TCCTAAGTATAACAG | 25853 |
rs184090612 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122632 | CAGGCACCCACCATC[A/G]TGCCCAGCTAATTTG | 25853 |
rs184196195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103711 | ATAGAAATAATTAAC[C/T]GGGTGTGGTGGTGTG | 25853 |
rs184215932 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123357 | TAAATAAGTAAGATA[C/T]TGCTCACTCAGAATA | 25853 |
rs184440196 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119295 | CAAACGATACTTTAT[C/T]AACAATACAGAAATT | 25853 |
rs184527570 | snp | G/T | 4.94222e-05 | 0.00497078 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125074 | ATTCAACCACTGAGA[G/T]GCAAACACTTTATTA | 25853 |
rs184592789 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104107 | AACCCTGTCTCTACC[A/C]AAAATACAAAAATTA | 25853 |
rs184838403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108191 | CAACTTAGAGAAATG[C/T]TTTATGGAAAAATCA | 25853 |
rs184943365 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088145 | AGATAGTAAAATTTT[C/G]ATTACCAAAGGGGAA | 25853 |
rs185004896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104371 | GCACATCTGGAGAAC[C/T]AGACATGGTTTGTTA | 25853 |
rs185009238 | snp | C/T | 0.000123115 | 0.00784489 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125657 | TCTCAGTCTGTACTC[C/T]CACTGGAGCACGGAA | 25853 |
rs185020916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095024 | AGCAAAGGTGTCCCA[C/T]GTGAAATTTTCCATT | 25853 |
rs185064139 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110819 | AACAAAACCAAGAGT[C/G]TCCTCAGTCCAGCCT | 25853 |
rs185199332 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095816 | CTTCAATTGCCAAAG[C/G/T]TTCCTAACACTCAGG | 25853 |
rs185206175 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115512 | GCTGAGGCAGGAGAA[G/T]TACTTGAACCCGGTA | 25853 |
rs185279415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118474 | GATGCTAACAGTTAA[C/T]GTGTAAGTTATTCAG | 25853 |
rs185287708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089954 | GCTTTTCTCCATCAT[A/G]TGTTTCCAACCTACA | 25853 |
rs185386501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099521 | ACAGGCATGAGCCAC[C/T]GCGCCTTACTCGAAA | 25853 |
rs185631090 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114727 | GGGGAAAGAGACATG[G/T]AAGACTAGTGAGTCT | 25853 |
rs185723764 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101781 | GCAACTTGGGAGGCT[A/G]AGGTAGGTGGACCGC | 25853 |
rs185731628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120802 | GACAAGGCCACTCTG[C/T]AACTGTGATAAAGAC | 25853 |
rs185758195 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094738 | GGTTTCACCATGTTA[C/G]CCAGGATGGTCTCAA | 25853 |
rs185916486 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100577 | TCAGCTCATCCCAAC[C/T]TCCACCTCCTGAGCA | 25853 |
rs186014914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126219 | CCAGTCCTGACCCTA[C/T]AGGCCCTGAACCCAT | 25853 |
rs186067414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104466 | CCTTGTATGCTGTGC[C/T]ATAAAATTTGTTTCT | 25853 |
rs186084356 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097162 | CCATAAATACAGATG[G/T]GATAGGAGGTTGAGG | 25853 |
rs186099979 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086162 | CCTGGGCATATCCAC[C/T]CTCAGCTGGACCTCA | 25853 |
rs186192117 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127439 | TCTTTTGTGCTTTAT[A/G]AAGTAGTCATCACGC | 25853 |
rs186229576 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101252 | AATTTTTTATTTTCA[C/T]TTTTTTGTAGAAATG | 25853 |
rs186355204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105201 | GAGGTTGTGGTGAGC[C/T]GAGGTCGTGCTACTG | 25853 |
rs186658538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091925 | GTTATTTAGCTGGCT[C/T]TAGGTCTTATATGTA | 25853 |
rs186704944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093994 | GCAAATCCTCAGTGG[A/G]TGCATACAACACATA | 25853 |
rs186721584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114056 | GAGCTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 25853 |
rs186927572 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120036 | GGTGAACCCTGTCTC[C/T]ACTAAAAAACAAAAA | 25853 |
rs186966630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116973 | AATAGCGCGAGACTC[C/T]GTCTCAAAAATCAAT | 25853 |
rs187036711 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093080 | TCTCAAACTCCCGAC[A/C]TCAGGTGATCCACCC | 25853 |
rs187046711 | snp | A/C | 0.00146523 | 0.0270271 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098552 | CAGATGTCAGATGTA[A/C]CCACCCCTCTATGGG | 25853 |
rs187055328 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117398 | CTCGTGATCTGCCTG[C/T]CTCGGCCGGCCAAAG | 25853 |
rs187143124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123614 | ATTAGGAAGACAGAA[A/G]GAGGTAGGAATTAAG | 25853 |
rs187164027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103867 | CAGTAACAACAACAA[C/T]GAAAATGTGTTTTAA | 25853 |
rs187194901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115845 | AGTCTCCCAAAGTGC[A/G]GGATTACAGACATAA | 25853 |
rs187244035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111303 | CTACTCTTTTACCTG[C/G]CCAACATGTACTTAT | 25853 |
rs187313339 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118836 | GGGCGTGGTGGCACA[C/G]ACCTGTAATCCCAGC | 25853 |
rs187349853 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128231 | CCCCAAATGTACCTT[A/G]TAGCAGAGCTCGCGA | 25853 |
rs187391797 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096228 | CAAAACAAAAAAAAC[A/C]ACCAGATGGGTGTGG | 25853 |
rs187521618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102566 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 25853 |
rs187547349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122873 | TTGCAGCCCCTACTA[C/T]TCCTTACTGTCTTGC | 25853 |
rs187633566 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102975 | CCCAGCTACTCAGGG[A/C]CAGGGGTGGGGTGCT | 25853 |
rs187776031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121727 | AGGCAGGCGGATCAC[A/G]AGGTCAGAAGATCGA | 25853 |
rs187779151 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086977 | TGGGAACAGCTGTTA[C/T]CTTTGACATGATGTG | 25853 |
rs187787490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106964 | ATTACTGGTAAATAT[C/T]AGTTTATATGGTTTA | 25853 |
rs187814557 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128053 | AATTCTGTCTTGCCC[C/T]GCAATGCTCTGGATG | 25853 |
rs187866130 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088181 | AAAGCAAAACAACTT[C/T]CAGATTTCTGTACAG | 25853 |
rs188025490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112417 | CCTGGCCAACATGAC[A/G]AAACCATCTCTACTA | 25853 |
rs188155067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108213 | GAAAAATCAGTCTTA[C/G]CGAAAGGACAGCCCT | 25853 |
rs188209043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095899 | TAAATGCATTGTTGA[A/G]GAGGACTGCTAGTCA | 25853 |
rs188215974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115564 | AGATAGCGCCACCGC[A/G]CTCCAGCCTGGCGAC | 25853 |
rs188289770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107960 | AAACTTTTAAACGAA[A/C]CACAATTCCCAGAAC | 25853 |
rs188300884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093519 | TATTGTTTCTGGACT[C/T]CCACCTTGATGGGCT | 25853 |
rs188358456 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100113 | AATCATAGCTCACTG[A/C]AGGCTCAACTTCCTG | 25853 |
rs188366852 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119037 | TATAACAGCATTAAG[A/C]CTTGAGGACCAGGAC | 25853 |
rs188567017 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087540 | TGTTTTAGGGGTGTG[G/T]CTACTGGCTAAGCAG | 25853 |
rs188720484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095221 | CTGGGACTACAGACG[C/T]CCACCACCACGCCCA | 25853 |
rs188867740 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099748 | ACAGGCACACGTCAC[A/C]ATGCCCGGCTAATTT | 25853 |
rs188932297 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118429 | GTGAGCCACTGCCCC[C/T]GGCCTGAAATTGATT | 25853 |
rs189104294 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099284 | CTGTGATGCCTAGGC[G/T]GGAGTGCAATGGCGC | 25853 |
rs189113112 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104166 | GCTACTTGGGAGGCC[A/C/G]AGGCAAGAGAAGTGT | 25853 |
rs189288879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104375 | ATCTGGAGAACTAGA[C/T]ATGGTTTGTTAATGC | 25853 |
rs189407152 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125091 | CAAACACTTTATTAA[A/G]GGTCCCAAGGTGAAA | 25853 |
rs189621597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088982 | GGGCACAGTGCATAT[A/G]CCTGTGGTCCCAGCT | 25853 |
rs189625441 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108472 | GAAGATATATGAAAG[A/G]AGAAACTAGGTGAGT | 25853 |
rs189684016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110141 | AAGGGGACAAACCAC[A/T]CTCAAACTGGCAACT | 25853 |
rs189776818 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115448 | TACAAAAAATTAGCC[A/G]GGCGGCTGGGCATGG | 25853 |
rs189934426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092553 | TAGCTGGGCGTGGTG[A/G]TGTGTGCCTGTAGTC | 25853 |
rs190040365 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109076 | TGTCAAGACATGAAG[A/C]ACAAGTGCACACACA | 25853 |
rs190184116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089961 | TCCATCATATGTTTC[C/T]AACCTACACTGCAAC | 25853 |
rs190201231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121153 | AGCGAGACTCCATCT[C/T]AAAAAACAAACAAAC | 25853 |
rs190281584 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094793 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTATAGG | 25853 |
rs190356942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098168 | TTCAGAGCCTCAGTT[A/G]TAATTTCTCACCAGC | 25853 |
rs190367782 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116974 | ATAGCGCGAGACTCC[A/C/G]TCTCAAAAATCAATC | 25853 |
rs190435182 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126822 | TTGGAAGATAGTTCT[C/G/T]TGGTGTTTCCCGGCC | 25853 |
rs190437813 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114763 | TGCATGCATTCATGT[C/G/T]TATCTAGACAAATGT | 25853 |
rs190581791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119445 | AGAGACAGGATTTTG[C/T]ATCTCATTTCATTAA | 25853 |
rs190700869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101308 | GTCTTGGACTCCTGA[A/C]CTCAAACTCCTGCTT | 25853 |
rs190711059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120329 | AAGCTGCAGTGAGCC[A/G]TGACTGCACCACTGT | 25853 |
rs190821748 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100578 | CAGCTCATCCCAACC[G/T]CCACCTCCTGAGCAC | 25853 |
rs190825487 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128061 | CTTGCCCCGCAATGC[C/T]CTGGATGACCCAAGA | 25853 |
rs190845824 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087318 | AATAGCAAAACCCAC[C/T]GGGGAGATTGGAAGA | 25853 |
rs190851877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107011 | CACCCTCCACTAGAA[C/T]GTAGGCTTCAAGAGG | 25853 |
rs190856825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105398 | GCCACTGCACTCCAG[C/T]CTGGGTGACAGAGCA | 25853 |
rs190989689 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092863 | CACCCCTTTTTTTTT[C/G]AGACAGAATTTCGCG | 25853 |
rs190999528 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111035 | CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGCATGA | 25853 |
rs191028013 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102261 | CACCAACAGTCTGGG[C/G]AACAGAGTAAGACCC | 25853 |
rs191041482 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127447 | GCTTTATGAAGTAGT[C/T]ATCACGCTGTAAACT | 25853 |
rs191099220 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086492 | CCCATTACAGAAGAG[C/G]GTCTAGCAATAGTAC | 25853 |
rs191278444 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114340 | GTCTGAGGCTGGTGG[A/G]TCACCTGAGGTCAGG | 25853 |
rs191431069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118266 | AGACTCCCGAGTAGC[C/T]GGGACCACAGGCATG | 25853 |
rs191440978 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088789 | CCTCCACCTGCTAGG[A/C]ACAGGAGGAAGAACC | 25853 |
rs191521964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098655 | TGGCCAGATGGCCCA[C/T]CCTAAACACAGAGCA | 25853 |
rs191625308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104844 | AAGTGCTTGAACCCA[A/G]GAGGCGGAGGTTGCA | 25853 |
rs191679982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111505 | TCTCCCAATTCTAAG[C/T]GCAGAGAATTTATCT | 25853 |
rs191747095 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093882 | CAGCTCACCTTCCCA[A/C/T]CTGAATGGGAATTGT | 25853 |
rs191757576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113483 | TCGCTGGGATGGCAG[A/G]TGCACACCACTGTGC | 25853 |
rs191823333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096884 | CCTTTATTCCTGTCT[C/T]GTGATGATTCCAGCA | 25853 |
rs191937280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099782 | TATTTTTAGTAGAGA[C/T]GGCGTTTCACCATGT | 25853 |
rs191944746 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118986 | GAAAATAATAATAAT[A/T]ATAATATCTCTCTTA | 25853 |
rs192071392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121925 | TCCAGCCTGGTGACA[C/T]AGCGAGACTCTGTCT | 25853 |
rs192102620 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103194 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 25853 |
rs192129449 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116410 | GCACAGTGGCTCACA[A/C]CTGTAATCCCAGCAC | 25853 |
rs192182524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123092 | ACAACAGTGGCTATC[C/T]TTGCTGTTACTGCTG | 25853 |
rs192338862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108245 | AGAAGAGTCAAACTC[C/T]TCAGTGATTCAACAG | 25853 |
rs192428643 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102749 | AAAATGGTATCTTTC[C/T]AGAGGACAACTGAGC | 25853 |
rs192517604 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108644 | TTACAAAATTAGCTG[G/T]GCATGGTGGCACACG | 25853 |
rs192697541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104044 | GAGGCCGATGCAGGC[A/G]GATCACTTGAAGTCA | 25853 |
rs192769076 | snp | C/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087649 | CACTTTGCAGTCCTG[C/G]CATGGGAGGCCCCAG | 25853 |
rs192780957 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128603 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC | 25853 |
rs192865969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123896 | AGGCCCGTTGCCACC[A/G]CTTAGTTTTGAAAGG | 25853 |
rs192918553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114847 | TAGCAGGAACCTATC[A/G]TCCCAGCTATTTGGG | 25853 |
rs192981234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108190 | TCAACTTAGAGAAAT[A/G]CTTTATGGAAAAATC | 25853 |
rs193088320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099340 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCCCAG | 25853 |
rs193160493 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094940 | TACACATAGAGTGAA[C/G]GTAATTTTATGCAAT | 25853 |
rs193249267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118468 | CTCAAGGATGCTAAC[A/C]GTTAACGTGTAAGTT | 25853 |
rs199551031 | in-del | -/ATG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109002 | TATATATATATATAT[-/ATG]GTTTTTTTTTTTTTC | 25853 |
rs199566614 | in-del | -/A | 0.0205511 | 0.0992634 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088275 | CCTCACACAATTAGG[-/A]AAAAAAAAAATCAAA | 25853 |
rs199596213 | snp | A/G | 0.00252875 | 0.035468 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098563 | TGTACCCACCCCTCT[A/G]TGGGAAATCCCACAG | 25853 |
rs199686194 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119099 | AAGAGCCCTCACCAG[A/G]GGCTATTTTGAGCTC | 25853 |
rs199712631 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109006 | TATATATATATATGG[G/T]TTTTTTTTTTTTCAC | 25853 |
rs199740255 | in-del | -/T | 0.47726 | 0.104176 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119703 | TATGTACTTTTGCGG[-/T]TTTTTTTTTTTTTTT | 25853 |
rs199806600 | snp | C/T | 3.30458e-05 | 0.0040647 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093456 | GAGAGGAGCTGAAAA[C/T]AGAGGAGAGATATAA | 25853 |
rs199814057 | snp | A/G | 0.000104572 | 0.00723013 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089372 | GAAGATAATTTTTCT[A/G]TTACTGTGTAGCAGT | 25853 |
rs200012788 | snp | A/T | 0.000560049 | 0.0167246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088529 | GGAAGAGAAAGAGAC[A/T]ACAATTAGCACCTCT | 25853 |
rs200020072 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088523 | TCTACGGGAAGAGAA[A/T]GAGACTACAATTAGC | 25853 |
rs200183336 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120391 | AAAACAACAAAGTGG[A/C]TGGGCATGGTGGCTC | 25853 |
rs200193400 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097980 | CCAAAGAGAAAAAAA[A/C]TGATTGTTTTCAGAA | 25853 |
rs200219078 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108802 | TGGTCTCAAAAAAAA[-/T]AAATAAATAAATATA | 25853 |
rs200233343 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102682 | AACAACAACAAAAAA[G/T]AAGAACACTTTTCTG | 25853 |
rs200261141 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118121 | AGATGGAAATTGATT[G/T]ATTTCTTTTGTTTTT | 25853 |
rs200281573 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098777 | TTATTTATTATTATT[-/A]TTTTTTTTTGAGACA | 25853 |
rs200315757 | snp | A/G | 8.23947e-05 | 0.00641799 | missense | DCAF12 | GRCh38.p7 | 9:34093421 | GACACACATTCTCAC[A/G]GCAATATGGCAGTTT | 25853 |
rs200387649 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100811 | AGCCTTATTTTTTTA[A/T]TTTTTTTTGTAGAGA | 25853 |
rs200427278 | snp | A/G | 1.67097e-05 | 0.00289043 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096802 | AGAGCAATGAAAACC[A/G]GGTTATATTATCATC | 25853 |
rs200429753 | in-del | -/AA/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108811 | AAAAATAAATAAATA[-/AA/T]AATATATATATATAT | 25853 |
rs200441585 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101057 | AGGGACCACAAACCC[C/T]CCCCAACTTTTTTTT | 25853 |
rs200551627 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091675 | AACCACAAAAAACCC[A/C]AAACAAAAGCTACTT | 25853 |
rs200588738 | snp | A/G | 0.000478165 | 0.0154549 | missense | DCAF12 | GRCh38.p7 | 9:34098469 | GCATCACTTTTGGTC[A/G]AAACATCATCTGTCA | 25853 |
rs200605585 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127418 | CCTGCCATCTAAACC[A/G]CATGGTCTTTTGTGC | 25853 |
rs200638541 | snp | A/C | 0.00137193 | 0.0261549 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124989 | CAATATATCCACGAC[A/C]TAGGAGAGAGGTCAC | 25853 |
rs200715393 | in-del | -/ATT | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124686 | GATGCTCTAAGCATC[-/ATT]ATTTCTTAAATCTTT | 25853 |
rs200790840 | snp | A/G | 0.330016 | 0.236849 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120690 | AAAAAAAAAAAAAGA[A/G]AACAAAGCAACCCTG | 25853 |
rs200796007 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088947 | GACCCCATCTCTACT[-/A]AAAAAAAAATAAATT | 25853 |
rs200880664 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091018 | TTCTAAAATGTAAGC[A/G]TTTTAACTATAATTA | 25853 |
rs200912036 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088024 | GTGAAGTAAGGGTGA[A/G]CTATGTCATTTCAGC | 25853 |
rs200920435 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097939 | ACACAGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 25853 |
rs200942946 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090675 | TTTCTCTTTTTTTTT[-/T]GAGCTCTGTTGCCAA | 25853 |
rs201084648 | in-del | -/ATATG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109000 | TATATATATATATAT[-/ATATG]GTTTTTTTTTTTTTC | 25853 |
rs201121166 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092708 | AAACAACAACAACAA[-/C]AAAAAAAGTAGAGCT | 25853 |
rs201192972 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122187 | CGACTTCCCACACCA[-/C]CCCCCCCAAAATCTT | 25853 |
rs201282914 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117257 | ATTTTTTTTTTTTTT[-/T]GAGATGGAGCTCAAA | 25853 |
rs201335289 | snp | C/T | 4.97418e-05 | 0.00498682 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093469 | AATAGAGGAGAGATA[C/T]AACCATGGCATCAGC | 25853 |
rs201440675 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123760 | AACACTATGATGCAC[A/G]TGCGGGGAGTGGAAT | 25853 |
rs201467111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102121 | ATGGCAAAACCCTGT[C/T]TCTACAAAAAATACA | 25853 |
rs201474188 | snp | C/T | 0.000116309 | 0.00762502 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125007 | GGAGAGAGGTCACAT[C/T]CCCCCAGGCACTTAC | 25853 |
rs201632211 | in-del | -/CACTTTA | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104881 | AAGATTGCACCATTG[-/CACTTTA]CACTTTAGCCTGGGC | 25853 |
rs201649141 | snp | A/G | 0.00199806 | 0.0315443 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089517 | TCTCTGAGCTCGGAT[A/G]TCATAGAACAGCAGG | 25853 |
rs201743439 | snp | A/G | 8.23716e-05 | 0.00641709 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125165 | CCATGCAACACTCGA[A/G]AGTAGCTGGTTTCAT | 25853 |
rs201774438 | snp | A/C | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088025 | TGAAGTAAGGGTGAG[A/C]TATGTCATTTCAGCC | 25853 |
rs201804628 | in-del | -/T | 0.381406 | 0.212679 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128418 | CTAATTTTTTTTTTT[-/T]CTTTTTTGAGACGGA | 25853 |
rs202100845 | in-del | -/AGAA | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088022 | AGTGAAGTAAGGGTG[-/AGAA]AGCTATGTCATTTCA | 25853 |
rs202171409 | snp | A/G | 0.00755512 | 0.0609957 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093258 | TGCAGTGCAGCTGTA[A/G]GCCTGAGGTGCACAC | 25853 |
rs202172047 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103406 | CTCAAAAAAAAAAAA[-/A]GAAACAAAAATAAAA | 25853 |
rs202193920 | in-del | -/CT | 0.0314385 | 0.121371 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097560 | TGCGCCTGGGTGACA[-/CT]CTGCTTTATTAAAAC | 25853 |
rs367585252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121563 | AAGAGTTCACGTCCA[A/G]AATTAAATACCTCCA | 25853 |
rs367763901 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089487 | ATAACAAGCTGAGAG[C/T]CTCTCTTCCAGAAAT | 25853 |
rs367801837 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107385 | ACACAGGATCCAGCG[C/T]AGGTAGTCGATAGAT | 25853 |
rs367832079 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103339 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 25853 |
rs367878640 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111318 | GCCAACATGTACTTA[C/T]CTTTCATGATTCGGT | 25853 |
rs367969182 | snp | C/T | 0.000156735 | 0.00885114 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126454 | AGCGCCGCCGCGGCC[C/T]CGCAGCCACATGGGG | 25853 |
rs367981564 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112487 | TAATCCTGGCTACTC[G/T]GGAGGCTGAGGCAGG | 25853 |
rs368084268 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094656 | CTGCCTCAGCTTCCC[A/G]GGTAGCTGGGACTAC | 25853 |
rs368155926 | snp | G/T | 0.000116738 | 0.00763906 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096794 | TTCCTACAAGAGCAA[G/T]GAAAACCAGGTTATA | 25853 |
rs368203372 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111940 | AGGAGTTCAAGACTA[C/G]CCTGGCAAACATGGT | 25853 |
rs368226320 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127949 | TGCGAAAGGCAGCTC[C/T]ATCTTATTTGGTCAG | 25853 |
rs368300161 | snp | A/G | 3.34482e-05 | 0.00408937 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124991 | ATATATCCACGACCT[A/G]GGAGAGAGGTCACAT | 25853 |
rs368321385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102801 | ATATTCCTGGCTGGG[C/T]GCAGTGGCTCACGAC | 25853 |
rs368341031 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34093428 | ATTCTCACGGCAATA[C/T]GGCAGTTTGGTGGAG | 25853 |
rs368506057 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115783 | GTGCCACTTTGTTGC[C/T]CATGTTGTAATAAAA | 25853 |
rs368535594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098188 | TTCTCACCAGCATCA[C/T]TCAGCCTTTAAGAGG | 25853 |
rs368609213 | snp | A/C | 5.03402e-05 | 0.00501673 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124976 | AGAGCAAGTGGAGCA[A/C]TATATCCACGACCTA | 25853 |
rs368685566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121774 | ACGGTGAAACCCTAT[C/T]TCTACTAAAAATACA | 25853 |
rs368715470 | snp | A/C/T | 4.9433e-05 | 0.00497137 | synonymous-codon, missense | DCAF12 | GRCh38.p7 | 9:34098450 | CCGTGACACATTGTG[A/C/T]CTCGCATCACTTTTG | 25853 |
rs368793595 | snp | A/G | 3.29516e-05 | 0.00405891 | missense | DCAF12 | GRCh38.p7 | 9:34088471 | TTGGGGAAGAAGTCA[A/G]TGTCTGAAAAGTAAT | 25853 |
rs368912661 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109183 | GCTCTAGGCCACCTC[C/T]TCATAGGCCCACTCC | 25853 |
rs368982645 | snp | C/T | 3.35661e-05 | 0.00409657 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125312 | AATCAGGGCTTTGGC[C/T]ACTCTTCTTCAGAAC | 25853 |
rs369040572 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092193 | ACAATATACGACACA[A/T]AAAGTATACAATTTG | 25853 |
rs369157735 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105375 | AGGCTGCAGTGAGCC[A/T]TGATGGTGCCACTGC | 25853 |
rs369164701 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119263 | ATAACAGTTTTAAAA[A/G]ATGAGTGTTTATTGT | 25853 |
rs369198546 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104441 | AGAAAGTTGGAAAGA[G/T]AGGTGTGGGCCTTGT | 25853 |
rs369390059 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096223 | CAAAACAAAACAAAA[A/C]AAACAACCAGATGGG | 25853 |
rs369665351 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108573 | AAGGCGGGCGGATCA[C/T]CAGAGCTTGAGAGTT | 25853 |
rs369683696 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119075 | TTGTGTATTTGCCCA[C/T]TGAGAATCAAGAGCC | 25853 |
rs369708705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117863 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATCAC | 25853 |
rs369725391 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089096 | CCAGCCTGGGCAACA[A/G]AGTGACCCTGTCTCA | 25853 |
rs369729112 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114438 | CTAAGAGTGTGCCCC[C/T]AACCTCACCCTCATT | 25853 |
rs369808092 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115592 | GACAGAGCAAGACTT[C/T]GTCTCAAAAAAAAAA | 25853 |
rs369814448 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100314 | CGCCATTCTCCTGCC[G/T]CAGCCTCCTGAGTAG | 25853 |
rs369817286 | snp | A/C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103633 | CTCAAGTGGGAGGAT[A/C/T]GCTTGAGCCTAGGAG | 25853 |
rs370031210 | in-del | -/TTAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101385 | GCCATAATTCCTTTA[-/TTAT]TTATTTATTTATTTT | 25853 |
rs370075311 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092972 | TGCCTCAGCCTCCTG[A/C]GCAGCTGGGATTACA | 25853 |
rs370117762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101889 | GGCGTGGTGGGGCAC[A/G]CCTGTGGTCCCAGCT | 25853 |
rs370233627 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113361 | GCGGCCTGAATTTTT[-/T]CTTATTTTTTTCTGA | 25853 |
rs370349419 | snp | A/T | 0.000153988 | 0.00877328 | missense | DCAF12 | GRCh38.p7 | 9:34093313 | CCCTGGAACAGACAG[A/T]CTTGACGTTGTATGA | 25853 |
rs370357295 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097965 | AAAAAGGAATGAATA[C/T]CAAAGAGAAAAAAAG | 25853 |
rs370378220 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121321 | ATAGAATTTGCCCGT[A/C]GTGACAGTATCCATC | 25853 |
rs370434786 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088691 | TTTTTCCAACTAAAC[A/G/T]TTAGAGAAGAACGGA | 25853 |
rs370604667 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088219 | TCCTATTAAGTGCCT[A/C]AACTATAGGCAAACT | 25853 |
rs370682494 | in-del | -/AGG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115380 | GCGGATCACGAGGTC[-/AGG]AGATCGAGACCATCC | 25853 |
rs370693262 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106542 | GAAAATAAGAAATTA[A/G]TAAAATAAGGATTGT | 25853 |
rs370703810 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119702 | TATGTACTTTTGCGG[-/T]TTTTTTTTTTTTTTT | 25853 |
rs370736334 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109000 | TATATATATATATAT[A/G]TATGGTTTTTTTTTT | 25853 |
rs370786246 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125911 | TTCTTTTGGGGTCCA[A/G]ACGCCGAAAGGCCCA | 25853 |
rs370834439 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092909 | GGAGTGCAATGGTGC[A/G]ATCTCAGCTCACCGC | 25853 |
rs370847662 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114744 | AGACTAGTGAGTCTA[C/T]CTCTGCATGCATTCA | 25853 |
rs370877352 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117113 | GTAATGGTACTTCAT[A/G]ATAGGTCTTGAATTC | 25853 |
rs371011929 | snp | A/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088026 | GAAGTAAGGGTGAGC[A/T]ATGTCATTTCAGCCT | 25853 |
rs371088209 | snp | C/G | 4.94271e-05 | 0.00497102 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088526 | ACGGGAAGAGAAAGA[C/G]ACTACAATTAGCACC | 25853 |
rs371173684 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106554 | TTAGTAAAATAAGGA[-/T]TGTAATAAACTCTCT | 25853 |
rs371185662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111634 | CTGTGAGGGTGAGGC[G/T]CTGTAGCTGTTTTAT | 25853 |
rs371213451 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127453 | TGAAGTAGTCATCAC[G/T]CTGTAAACTTATCTG | 25853 |
rs371249428 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103368 | GCTAAGACATGGCCA[C/T]TGCACTCCAGCTGGG | 25853 |
rs371288645 | snp | A/G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101727 | TGACTGTTCTAGACC[A/G/T]TTCTTTATTAAGAAT | 25853 |
rs371468894 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121673 | TTTTCGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 25853 |
rs371477186 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126565 | AATGGCCCGGACCCG[A/G]AGCGGCAGCAGAAAA | 25853 |
rs371492912 | snp | C/T | 2.40399e-05 | 0.0034669 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126470 | CGCAGCCACATGGGG[C/T]GGGGGAAGCGAAGGA | 25853 |
rs371500953 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102604 | GTTGCAGTGAGCCGA[G/T]ATCACACCACTGCAC | 25853 |
rs371651057 | snp | A/G | 6.90036e-05 | 0.00587342 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089389 | TACTGTGTAGCAGTC[A/G]TCTCAGGTAGGGGCT | 25853 |
rs371708410 | snp | C/G | 4.9436e-05 | 0.00497148 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125232 | CTAAGGATCTCTTCA[C/G]AGGAGGAAGTCTTTT | 25853 |
rs371723555 | snp | C/G | 3.37149e-05 | 0.00410564 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098311 | CGTCAGGGATCCCTA[C/G]ACAAGTTCATACCTT | 25853 |
rs371731126 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125803 | CCGCCAACGGGGTAG[C/T]AGGCCCCCGGGAAAT | 25853 |
rs371758058 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118236 | CCTCCCGGGTTCAAG[C/T]GACTGTCCTGACTCA | 25853 |
rs371760320 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120789 | AATATCAACATCAGA[C/T]AAGGCCACTCTGCAA | 25853 |
rs371845331 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112557 | CGAGATCACACCACT[A/G]CACTCCAGCCTGGGC | 25853 |
rs372057124 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093531 | ACTCCCACCTTGATG[A/G]GCTTCCCTCATATAA | 25853 |
rs372231871 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094676 | GCTGGGACTACAAGC[A/G]CCCACCACCACGCCC | 25853 |
rs372380479 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124979 | GCAAGTGGAGCAATA[C/T]ATCCACGACCTAGGA | 25853 |
rs372464486 | snp | C/G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112251 | TTCTGTTCTTGGGGT[C/G/T]TGTGAACTCGTCTTT | 25853 |
rs372474110 | snp | A/C/G | 0.000165553 | 0.00909676 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093465 | TGAAAATAGAGGAGA[A/C/G]ATATAACCATGGCAT | 25853 |
rs372476727 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092992 | CTGGGATTACAGGCA[C/T]GCGCCACTGCGCCCG | 25853 |
rs372502228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104135 | TTAGGCACAGTGGCA[C/T]GCACCTGTAGTCCCA | 25853 |
rs372578810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088922 | TGAGACCAGCCTGGG[A/C]AACATGGCGAGACCC | 25853 |
rs372610463 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092232 | ACATATGTATATATC[C/T]ATGACATCATAACCA | 25853 |
rs372615412 | snp | A/C | 1.68303e-05 | 0.00290084 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125316 | AGGGCTTTGGCTACT[A/C]TTCTTCAGAACAGAT | 25853 |
rs372624056 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107463 | AAGGATTCAGCTCGA[C/T]GGCATGGATACCACA | 25853 |
rs372626461 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127243 | CGAGTCTCTGGCTAC[C/T]CTCTTCCCACCGCTG | 25853 |
rs372728850 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118925 | AGCCAAGATTGCGCC[A/G]GTGCACTGCAGCCTG | 25853 |
rs372747621 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126145 | GATTATGTCCCATTC[C/T]TGAGTTCCCCTTTGG | 25853 |
rs372768992 | snp | C/T | 0.000116425 | 0.00762883 | missense | DCAF12 | GRCh38.p7 | 9:34098500 | CCTCCCAGAGTCCCA[C/T]AGAACCATCACGTGA | 25853 |
rs372911448 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102666 | AACAAACACACAAAC[A/C]AACAACAACAAAAAA | 25853 |
rs372946636 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090175 | TTCAAGCGATTCTCC[C/T]GCCTTAGCCTCCCAA | 25853 |
rs373170598 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096339 | ATCCATGAGCCATGA[A/C]TGCACTCCAACTTGG | 25853 |
rs373216067 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095108 | TGAGAGAGAGTCTTG[C/T]TCTGTTGCCAGGCTG | 25853 |
rs373271009 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101972 | AGTGAGCTGAAATTG[A/T]GCCACAGACTCCAAC | 25853 |
rs373278094 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116772 | GATCACTCTAGGTCA[C/G]AAGTTTGAGACCATC | 25853 |
rs373326668 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105841 | GCAACCTCTGCCTGC[C/T]GGGTTCAAGCAATTC | 25853 |
rs373333816 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112790 | GTAATCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 25853 |
rs373382716 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095681 | GGCCTAAGGTATTGT[A/G]CCCAACTGGATTTTG | 25853 |
rs373521114 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124384 | TTTATCCTGGCCTAT[A/G]ATTGGGTTGGTTACA | 25853 |
rs373541525 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115895 | ACATACCTTTAACGG[C/T]GATAAGGTAGTTCAC | 25853 |
rs373663726 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127038 | GTTACCTCCCATCTG[A/G]CACCAAACGTTTCCC | 25853 |
rs373695590 | in-del | -/T | 0.478768 | 0.100824 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109006 | TATATATATATATGG[-/T]TTTTTTTTTTTTCAC | 25853 |
rs373737543 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107442 | CAGTGGCTAGCAGTG[C/T]TCTAGAAGGATTCAG | 25853 |
rs373810308 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087674 | CCCCAGGAAGCCTAC[A/G]ATCTAACTAAAAAGA | 25853 |
rs373903746 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119383 | GTCAGGTTCCTGTTT[A/G]GTCTTCAACCACATA | 25853 |
rs374048315 | snp | C/T | 3.32734e-05 | 0.00407868 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093481 | ATATAACCATGGCAT[C/T]AGCAGAGAGGGTAAG | 25853 |
rs374102358 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124975 | TAGAGCAAGTGGAGC[A/T]ATATATCCACGACCT | 25853 |
rs374118409 | in-del | -/CTTAA | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126049 | TTTGTTTCCGATTCC[-/CTTAA]CTTCGGTTTCCCCTT | 25853 |
rs374130168 | snp | A/G | 0.000110538 | 0.00743349 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089619 | AAGTAAAAGGCAGTG[A/G]GGCGGGAGAGAATAT | 25853 |
rs374130828 | snp | A/G | 0.000115307 | 0.00759211 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107384 | CACACAGGATCCAGC[A/G]TAGGTAGTCGATAGA | 25853 |
rs374161194 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34093356 | ATCCAAGAAGGAGAC[A/G]TGAGCTTGGGAGCCC | 25853 |
rs374183998 | in-del | -/GAG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115382 | GGATCACGAGGTCAG[-/GAG]ATCGAGACCATCCTG | 25853 |
rs374267387 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106156 | GGAGTGCAGTGGCAC[A/G]ATCACAGCTTGATGC | 25853 |
rs374334722 | in-del | -/AG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101783 | ACTTGGGAGGCTGAG[-/AG]GTAGGTGGACCGCCT | 25853 |
rs374434094 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107971 | CGAAACACAATTCCC[A/G]GAACACATCATGGCT | 25853 |
rs374455243 | in-del | -/AGT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092394 | TACCACAGGATAGAA[-/AGT]AGGGCTCTCGGCCAG | 25853 |
rs374699900 | snp | C/G/T | 0.0337553 | 0.125452 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127110 | AGGGGGGTGGGGGGG[C/G/T]GGGGGGCAGGAACCG | 25853 |
rs374707804 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119319 | AGAAATTTAAAATGC[A/T]AGAAAGATCACTCAG | 25853 |
rs374748645 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115319 | TATAGCGGCTAGGCG[C/T]GGTGGCTCACACCTG | 25853 |
rs374750875 | snp | A/G | 1.74093e-05 | 0.00295031 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107588 | AAAAAATGGATACAG[A/G]AGCTGAACATAAATT | 25853 |
rs374752366 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096820 | TTATATTATCATCTA[C/T]AGCAACTAATGTACG | 25853 |
rs375189578 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101064 | ACAAACCCTCCCCAA[A/C]TTTTTTTTTTTTTTT | 25853 |
rs375301051 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100300 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 25853 |
rs375304252 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091585 | AAAAGCTGCAGTGAA[C/T]TGAGATTGCACCACT | 25853 |
rs375496786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112857 | AAGCTGAGATCACGC[C/T]ATTGCACTCCAACCT | 25853 |
rs375504185 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094617 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 25853 |
rs375576633 | snp | A/G | 5.39933e-05 | 0.00519555 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088326 | TGGAAGTTAGTGTAA[A/G]TCTCTGCATTTGGGG | 25853 |
rs375670033 | in-del | -/A | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086012 | TCCAACTACAAAAAA[-/A]CAAAAATTAATATCC | 25853 |
rs375672198 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124985 | GGAGCAATATATCCA[C/T]GACCTAGGAGAGAGG | 25853 |
rs375769146 | snp | A/G | 4.98144e-05 | 0.00499047 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125283 | CCCAGCCAAACTGTG[A/G]AAACAACATTAGAAA | 25853 |
rs375792276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112673 | GGAGGCCGAGGAGGG[C/T]GGATCATCTGAGGTT | 25853 |
rs375833296 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099053 | AGGATTACAGGTGTG[A/T]GCCACCACACCTGGT | 25853 |
rs375908049 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086437 | AAAGTCAAGTGCTAC[A/G]TTTTTAAAAACAGAA | 25853 |
rs376007686 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114682 | GTAAGCTCGAGGCTC[A/G]GGCTCCCTGCAGTTT | 25853 |
rs376012211 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106559 | AAAATAAGGATTGTA[A/G]TAAACTCTCTAAAGA | 25853 |
rs376042195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109911 | CTGGTGGACGGAGAG[A/G]GTGACATTGTAGGGC | 25853 |
rs376064347 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107470 | CAGCTCGATGGCATG[A/G]ATACCACAGCCCTGC | 25853 |
rs376139003 | snp | C/T | 8.01459e-05 | 0.00632981 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106464 | TGTCGCTGATCCATG[C/T]GATGGAAAAGATCCA | 25853 |
rs376182314 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109083 | ACATGAAGAACAAGT[G/T]CACACACAGACATGG | 25853 |
rs376289249 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112886 | CTGGGCAATAAGAGC[A/G]AAACTCTGTCTCAAA | 25853 |
rs376312875 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109707 | GAAGTGCAAGCGGGG[A/G]AATAGGACCCTGTTC | 25853 |
rs376317850 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121270 | TTATCAATTACAGCT[C/T]TAACCTCCTGCTAGA | 25853 |
rs376385738 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116025 | TTTTATTGAAATCCA[G/T]GGCCTCCTCTTAGTA | 25853 |
rs376415452 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091359 | AAAGAAATAGCTGGG[C/T]ACAGTGGCTCACGGC | 25853 |
rs376515921 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126762 | GCACTTCGGATAGCG[C/T]CGCCACGGAAACACC | 25853 |
rs376634435 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114750 | GTGAGTCTATCTCTG[C/T]ATGCATTCATGTGTA | 25853 |
rs376684023 | snp | A/G | 3.29707e-05 | 0.00406008 | stop-gained | DCAF12 | GRCh38.p7 | 9:34089513 | GAAATCTCTGAGCTC[A/G]GATGTCATAGAACAG | 25853 |
rs376731358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119218 | CACCGTCATTTTAGG[A/G]TAAGAAAACGCAAGG | 25853 |
rs376742485 | snp | C/G | 0.0170251 | 0.090679 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087256 | CTACACACAGATAAA[C/G]CCCCTGCTCACCCCC | 25853 |
rs376744500 | snp | C/T | 3.35121e-05 | 0.00409328 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125308 | TAGAAATCAGGGCTT[C/T]GGCTACTCTTCTTCA | 25853 |
rs376826818 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113180 | CTCAGCCTCGCCGAG[C/T]ACCTGGGATTACAGG | 25853 |
rs376906522 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108710 | AGAATCGCTTGAACC[A/G]AGGAGGCGGAGGTTG | 25853 |
rs376906615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096835 | TAGCAACTAATGTAC[A/G]ATAATAAGCAGGCGA | 25853 |
rs376925774 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091639 | TGAGGACCCTGTCTT[A/C]AAAAAAAAAAAAAAA | 25853 |
rs376932327 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087546 | AGGGGTGTGGCTACT[A/G]GCTAAGCAGATGTGA | 25853 |
rs376972936 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120689 | AAAAAAAAAAAAAAG[A/G]AAACAAAGCAACCCT | 25853 |
rs377069694 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108492 | ACTAGGTGAGTCTTA[A/G]GTTTAAAATATAAAA | 25853 |
rs377100113 | snp | C/G/T | 9.32385e-05 | 0.00682731 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089622 | TAAAAGGCAGTGAGG[C/G/T]GGGAGAGAATATTTG | 25853 |
rs377155209 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115082 | AAGTAATTCTACGCA[A/G]GTCACACAGACAACA | 25853 |
rs377166525 | snp | A/T | 1.64792e-05 | 0.00287042 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107331 | AAAAACAAGGCTCCC[A/T]CCAACTACAACTACT | 25853 |
rs377324945 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118946 | CTGCAGCCTGGGCAA[C/G]AGAGTAAGACCCTGT | 25853 |
rs377329450 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106428 | CCTATAAAAGGGCAA[C/T]TTTACCAGACACTGC | 25853 |
rs377401755 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115584 | AGCCTGGCGACAGAG[C/T]AAGACTTCGTCTCAA | 25853 |
rs377428083 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092396 | CCACAGGATAGAAAG[C/T]AGGGCTCTCGGCCAG | 25853 |
rs377504137 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108812 | AAAATAAATAAATAA[-/AT]ATATATATATATATA | 25853 |
rs377530676 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105999 | ATAATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 25853 |
rs377534714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095998 | TGCAAGAGAGGCACA[A/C]CAGACTCAAAATTTC | 25853 |
rs377598926 | in-del | -/TTAGCCGGGCG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115442 | TAAAAATACAAAAAA[-/TTAGCCGGGCG]GCTGGGCATGGTGGC | 25853 |
rs386734394 | multinucleotide-polymorphism | CGAGT/TGAGC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092970 | CCTGCCTCAGCCTCC[CGAGT/TGAGC]AGCTGGGATTACAGG | 25853 |
rs386734395 | multinucleotide-polymorphism | GGCG/TACT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115513 | CTGAGGCAGGAGAAT[GGCG/TACT]TGAACCCGGTAGGCG | 25853 |
rs386734396 | multinucleotide-polymorphism | GT/TG | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126790 | ACCGCCGGAACGAGA[GT/TG]GGCGGGATCTAGGGG | 25853 |
rs397780479 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114118 | GTCTCAAAAAAAAAA[-/A]ATGTGGCACAGATAC | 25853 |
rs397806905 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114119 | TCTCAAAAAAAAAAA[-/A]TGTGGCACAGATACA | 25853 |
rs398010663 | in-del | -/T | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120233 | CCATCATACCTGGCC[-/T]TTTTTTTTTTTTTTT | 25853 |
rs398046544 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095093 | GGAGGCTTTTTTTTT[-/T]GAGAGAGAGTCTTGC | 25853 |
rs398113430 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102294 | CTCCAAAAAAAAAAA[-/A]GAATAATGACTGTTT | 25853 |
rs527270676 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089472 | TCTGGGCTTGGACCC[A/G]TAACAAGCTGAGAGC | 25853 |
rs527324715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095288 | CCATGTTGGCCAGCA[G/T]GGTCTCAATCTCTTG | 25853 |
rs527344486 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090125 | CTGGAGTGCAATGGC[A/G]CGATCTTGGCTCGCT | 25853 |
rs527456807 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112819 | AGGTGAATCGCTTGA[A/C]CCCGGGAGGCAGAGG | 25853 |
rs527480318 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114138 | GGCACAGATACACAA[C/T]GCAATACTGTTTAGC | 25853 |
rs527494712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112463 | GCCAGGTGTGGTGGC[A/G]TGAGTCTGTAATCCT | 25853 |
rs527522318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122968 | AGTCTAAACCATGAA[C/T]ATATACCTAACCCAT | 25853 |
rs527587325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123807 | GAGACTCTTTTTCTA[C/G]TCCAAGTGACAAGGA | 25853 |
rs527644388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120464 | TTACATGAGGTCAGG[C/T]GTTTGAGACCAGCCT | 25853 |
rs527690040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088609 | CTCCTTAAGGGAACA[C/G]GGTTCTACAGGTACA | 25853 |
rs527703223 | in-del | -/CCT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115467 | GGCTGGGCATGGTGG[-/CCT]GCACCTGTAGTCCCA | 25853 |
rs527803659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121037 | CATGTGCCCGTACTC[C/T]CAGCCACTCGGGAGG | 25853 |
rs527963117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101958 | GAAGTAGAAGTTGCA[A/G]TGAGCTGAAATTGTG | 25853 |
rs527998355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109054 | TGGAGTGTCTTTAGA[C/G]CTGTGATGTCAAGAC | 25853 |
rs528114461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125814 | GTAGTAGGCCCCCGG[A/G]AAATCAGAGGCCATA | 25853 |
rs528124195 | in-del | -/A | 0.391769 | 0.205917 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103405 | GGAGGACTCCATCTC[-/A]AAAAAAAAAAAAGAA | 25853 |
rs528151641 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112003 | AAAAAATTAGCTGGA[C/T]GTGGTGGCGGGCGCC | 25853 |
rs528175164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118270 | TCCCGAGTAGCCGGG[A/G]CCACAGGCATGCGGC | 25853 |
rs528370238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099001 | TCTTGAACTCCTGAG[A/T]TCCAGCGATCAGCCT | 25853 |
rs528576244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103641 | GGAGGATCGCTTGAG[A/C]CTAGGAGTTTGACAG | 25853 |
rs528699038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097447 | TTTTCAGTAAACATG[A/G]GGTTTTACCATGTTG | 25853 |
rs528743323 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092453 | AGCACTTTGGAAGGC[C/T]GAGGTGGGTGGATCA | 25853 |
rs528787601 | in-del | -/CTTTT | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128255 | CTCGCGATTTCTTTT[-/CTTTT]TTTTTTTTTGAGATG | 25853 |
rs528845590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123974 | TTGGCCCCAACCACC[A/G]TGGTATTATTTCCTT | 25853 |
rs528887106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091836 | GGGATAAAGTGAGAT[A/G]AAGAAAATACAATTT | 25853 |
rs528936797 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115202 | AGAAGAATCTATTCA[C/T]TATCCCAATCTGAGA | 25853 |
rs528969738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117407 | TGCCTGCCTCGGCCG[A/G]CCAAAGTGCTGGCAT | 25853 |
rs529009446 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124677 | ATCCTGAATGATGCT[C/T]TAAGCATCATTATTT | 25853 |
rs529121243 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118227 | CAACCTCTGCCTCCC[G/T]GGTTCAAGCGACTGT | 25853 |
rs529146787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111233 | TTGTGATCCACCTGC[C/T]TCAGCCTCCCAAAGT | 25853 |
rs529174232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104913 | ACACAGCAAGACTCC[A/G]TCTCCAAAAAAAAAA | 25853 |
rs529212589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104178 | GCCGAGGCAAGAGAA[A/G]TGTTTGAACCTGGGA | 25853 |
rs529266935 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111860 | GAAGCATGGGCCAGG[C/T]GCAGTGGCTTATGCC | 25853 |
rs529300402 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086471 | CTCAAACAATCAAAC[A/G]CATTACCCATTACAG | 25853 |
rs529315976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110124 | GTGGGAGCAGGGGGA[A/G]GAAGGGGACAAACCA | 25853 |
rs529317921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102802 | TATTCCTGGCTGGGC[A/G]CAGTGGCTCACGACT | 25853 |
rs529332902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116168 | TTCAAGACCAGCCTG[A/G]CAAACATGGCAAACC | 25853 |
rs529355645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109727 | GGACCCTGTTCATGG[C/G]CATTGAGCTGGCCCT | 25853 |
rs529505032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096227 | ACAAAACAAAAAAAA[A/C]AACCAGATGGGTGTG | 25853 |
rs529577754 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098117 | AATATAGACTACTCA[-/C]GAGAAATACTGCAGA | 25853 |
rs529703578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113347 | ATGGGCCACTGTACG[C/T]GGCCTGAATTTTTTC | 25853 |
rs529807002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113975 | TAGCCGGGCGTGGTG[A/G]TGGGTACCTGTAGTC | 25853 |
rs529913342 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087729 | CTTTCTGTTTTTACT[C/T]CCTATTATCAGTGTT | 25853 |
rs529938713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093544 | TGGGCTTCCCTCATA[C/T]AAAAGCCACATAAAA | 25853 |
rs529965863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094748 | TGTTAGCCAGGATGG[C/T]CTCAATCTCCTGACC | 25853 |
rs530052288 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100365 | ACCACGCCTGGCTAA[-/T]TTTTTTGTATTTTTA | 25853 |
rs530099359 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119748 | GCTCTGTCACCCAGG[C/T]TAGAGTGCAGTGGTG | 25853 |
rs530104401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092993 | TGGGATTACAGGCAT[A/G]CGCCACTGCGCCCGG | 25853 |
rs530117025 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108613 | CCTGGCTAACATGGT[A/G]AAAACCCTACTAAAC | 25853 |
rs530237676 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102541 | GCCTGTAATCCCAGA[C/T]ACTTAGGAGGCTGAG | 25853 |
rs530278519 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126795 | CGGAACGAGATGGGC[A/G]GGATCTAGGGGTTGG | 25853 |
rs530299510 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124522 | CCAGACACACATTCC[C/T]TGCCTTCCTTATAGG | 25853 |
rs530426874 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100533 | AAGGCCTCACTCTGT[G/T]GCCCAGGCTGGAGTG | 25853 |
rs530447291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119007 | ATCTCTCTTATCTCA[C/T]ACTTACTTCCTAAGT | 25853 |
rs530465481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118921 | AGTGAGCCAAGATTG[C/T]GCCAGTGCACTGCAG | 25853 |
rs530526132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112572 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGAATC | 25853 |
rs530601306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099517 | GATTACAGGCATGAG[C/G]CACCGCGCCTTACTC | 25853 |
rs530802697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104799 | GTGGGCACCTGTAAT[C/T]CCAGCTACTCAGGAG | 25853 |
rs530906276 | in-del | -/TTTC | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128252 | GAGCTCGCGATTTCT[-/TTTC]TTTTTTTTTTTTTGA | 25853 |
rs530918122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097508 | TGATCTGCCTGCCTC[A/G]GCCTCCGAAAGTGCA | 25853 |
rs531018673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092603 | AGGCAGGAGAATCAC[C/T]TGAACTCAGAAGGCA | 25853 |
rs531079818 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105185 | TCGAACCTGGGAAGC[A/C/G]GAGGTTGTGGTGAGC | 25853 |
rs531089936 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126727 | CCCCCTTGCTCGCGC[G/T]CCGTCACCCTTGCGC | 25853 |
rs531256739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126009 | TTCCTAGGGCCCATG[C/G]AAGGTAGAGTTCACT | 25853 |
rs531330589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101726 | ATGACTGTTCTAGAC[C/T]GTTCTTTATTAAGAA | 25853 |
rs531405200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095232 | GACGCCCACCACCAC[A/G]CCCAGCTAATTTTTG | 25853 |
rs531488939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115363 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 25853 |
rs531512035 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111471 | TACTTATTTGTCTTC[C/T]TCATAAAGCTATTAA | 25853 |
rs531604960 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114583 | GGGTCCAAGGATTCA[C/T]GCAGCTCCACTAACA | 25853 |
rs531689304 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127945 | GTCTTGCGAAAGGCA[A/G]CTCCATCTTATTTGG | 25853 |
rs531695823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120355 | ACTGTACTCCACCCT[A/G]AGTGCAAAATGCTGT | 25853 |
rs531736160 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128421 | TTGCCCAGCTAATTT[C/T]TTTTTTTCTTTTTTG | 25853 |
rs531739604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094061 | TGTGACATGAAGGAA[C/T]CACTAATTCCTGGAA | 25853 |
rs531747865 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087147 | AGGCCAGCCTGTCAC[C/T]ATCTCAGGGCTAAGC | 25853 |
rs531978610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120951 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 25853 |
rs531989057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114131 | AAAATGTGGCACAGA[C/T]ACACAATGCAATACT | 25853 |
rs532001875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100388 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 25853 |
rs532050443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107717 | GCATGGTCAGGACTA[C/T]TAATGACATGAAACA | 25853 |
rs532051031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094220 | GACCAGGCTGGCCAA[A/C]CTGGTGAGATGCCAT | 25853 |
rs532120678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116700 | TTAATAAATAAATCC[A/G]GCCGGGCACGGTGGC | 25853 |
rs532185273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100931 | GGCATGAGCCACCAT[A/G]CCCAGACTAGGCCTC | 25853 |
rs532187036 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094766 | CAATCTCCTGACCTT[A/G]CGATCCGCCCACCTT | 25853 |
rs532207780 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097284 | TTTTTTTTTTTGAGA[G/T]GGAGTCTTGCTCTGT | 25853 |
rs532388346 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128326 | CACGATCTCGGCTCA[C/T]TGCAACCTCTGCCTC | 25853 |
rs532464547 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086968 | ACTGGTGGGTGGGAA[C/T]AGCTGTTATCTTTGA | 25853 |
rs532474936 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127797 | TCAGGCCTCATACCT[A/C]CAAGGAGCTCTGTTG | 25853 |
rs532562103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093033 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATAT | 25853 |
rs532588614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099408 | AGTTAATTTTTGTAT[G/T]TTTAGTAGAGATTGG | 25853 |
rs532717536 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100777 | AGTGCTGGGATTACA[C/G]GTATGAGCCACCAAG | 25853 |
rs532955881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091254 | ATCGCTTGAACCTGG[A/G]AGGCAGAGGGTGCAG | 25853 |
rs532957787 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112029 | GCGCCTGTAATCCCA[C/G]CTACTCGGGAGGCTG | 25853 |
rs532968256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090157 | CAACCTCTGCCTTCC[A/G]GGTTCAAGCGATTCT | 25853 |
rs533021907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124593 | TTAGATTCTGTTCAC[C/T]AAAAAACAGCCAAGT | 25853 |
rs533026879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123845 | TCTTAACCACGAGTG[A/G]GCAGCTGGAGAGACC | 25853 |
rs533166953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092205 | ACATAAAGTATACAA[C/T]TTGAGGTTCTGACAT | 25853 |
rs533197369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121853 | GAGGCTGAGGCGGGA[A/G]AATCGATTGAACCCA | 25853 |
rs533236479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109153 | TCACTTCTTCCCTTT[A/G]CCCAAAAACAGAAGG | 25853 |
rs533270916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117401 | GTGATCTGCCTGCCT[C/T]GGCCGGCCAAAGTGC | 25853 |
rs533298945 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104656 | TGCAGTGGCTCATGC[A/C]TGTAATCCCAGCATT | 25853 |
rs533390287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102041 | AAAGATAATAATGAC[A/G]ACTATTCTAGGCTGG | 25853 |
rs533531090 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108672 | ACGCCTGTAATCTCA[G/T]CTACTCGGGAGGCTG | 25853 |
rs533627408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115052 | TGTTTCAGACTGGAG[C/T]CCAATGAGAAAGGAA | 25853 |
rs533810398 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109812 | GACACCATAGGTGGG[C/T]GTGGGCAGCTTTAGG | 25853 |
rs533821850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088852 | CAGTGGTTCATGGCT[A/G]TAATCCCAGAATTTT | 25853 |
rs533883849 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088164 | ACCAAAGGGGAAAAC[A/G]AAAAGCAAAACAACT | 25853 |
rs533886350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121435 | ACCGAGAGGTCCCTC[A/G]CTCTCTTATGGTGAA | 25853 |
rs533977850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113770 | TCACAATAGCCAAGA[C/T]ACGGAATCAGCCGAA | 25853 |
rs534033332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115562 | CGAGATAGCGCCACC[A/G]CACTCCAGCCTGGCG | 25853 |
rs534093684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109447 | AGACAGCTGTTTTCA[C/T]CTTGTGGGGGATTCA | 25853 |
rs534178086 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088338 | TAAATCTCTGCATTT[C/G]GGGAGTTGTCATTAA | 25853 |
rs534247635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099860 | ACCTCCCAAAGTGCT[A/G]GGATTACAGGCATAA | 25853 |