SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs534272590 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107966 | TTAAACGAAACACAA[C/T]TCCCAGAACACATCA | 25853 |
rs534325338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114185 | ATCCTTTGGACAACA[C/T]GGATGAACCTAGAGG | 25853 |
rs534354483 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117534 | CCTTGATTTTACCTA[A/G/T]TACCCACCAAAGTCA | 25853 |
rs534437716 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113418 | CTGGAATGCAGTGGC[A/G]TGATCTTGGCTCCCG | 25853 |
rs534456294 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094822 | GGCGTGAGCCACCGC[A/G]CCCGGCCCCGATTTT | 25853 |
rs534507101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101230 | GCATGTATCCTCATG[C/T]CCAGGTAATTTTTTA | 25853 |
rs534653534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110601 | AGCATGGCATTAAGA[C/T]TCTCCTCGGGGCCAG | 25853 |
rs534685686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096321 | GAGTTCAAGGCTGCA[C/T]TGATCCATGAGCCAT | 25853 |
rs534715205 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091427 | TGAGGTGGGTGTCCC[-/A]AGAGTTTGAGACAAC | 25853 |
rs534718514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103859 | AACAACAACAGTAAC[A/G]ACAACAACGAAAATG | 25853 |
rs534744883 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095737 | ATTTGTATTGTAAAT[G/T]AAGTCTATTTTCTCA | 25853 |
rs534795119 | snp | A/G | 0.000121632 | 0.00779752 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125580 | GAAAGATTGAAGGAA[A/G]TGAGAGGTAGAGTGA | 25853 |
rs534862722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097724 | GATCAACTGAGGTCA[C/G]GAGTTCAAGACCAGC | 25853 |
rs534864590 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122849 | GTCAAGAATGCCTTC[C/T]GTAGTTCTTTGCAGC | 25853 |
rs534961988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117059 | GAATCTAAACTGTTC[C/G]TACACAAGATGGACT | 25853 |
rs535091948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090550 | CACATAAGAACTGGA[C/T]AATATTTGTGGAACC | 25853 |
rs535221005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117022 | TCTGCGCTATGCCAA[G/T]ATCTTAGACACTCTG | 25853 |
rs535502648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109278 | CTCAGTGAACTCCAT[C/T]TCATCCATGCCACTT | 25853 |
rs535527288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101452 | GGCTAGAATGCAATG[A/G]CACGATCTTGGCTCA | 25853 |
rs535528583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103162 | CATGCCTGTAATCCC[A/G]GCACTTTAGGAGGCC | 25853 |
rs535528616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110468 | CCTTCAGGCAACACC[A/G]CTATCAAAATTATTC | 25853 |
rs535592434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094974 | TTAAATAATTTTCTG[C/T]ATTAAACAATGTTTG | 25853 |
rs535653650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090214 | GATTACAGGCTCCTG[C/G]CATCACACTCAGCTA | 25853 |
rs535689361 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103900 | TTCTTTTTCCAGTAA[A/C]CTTATTTGCCAGTTC | 25853 |
rs535692946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091543 | CGGGAGGCTGAGGTG[A/G]GAGGACTGCTTGAGC | 25853 |
rs535695555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103774 | TTAATCCTGGGAGTT[C/T]GAGGTTGCAGTGAGC | 25853 |
rs535745690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106338 | GTGAGTCACTGAGCC[C/T]GGCTGGGCTGTTTCC | 25853 |
rs535756949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096933 | AGACCATTACTTCAC[C/T]CTACAGAACCTAGCT | 25853 |
rs535810763 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095061 | ATTGTGTTGGTGCTC[-/A]AAAAGTTTTGGACTT | 25853 |
rs535870763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098581 | GGAAATCCCACAGAC[A/G]CCAAAGAGGGCTTTC | 25853 |
rs535891512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105811 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 25853 |
rs535924835 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108064 | AATTATTAGTATCTC[A/G]TGGCTGTTCTCTATA | 25853 |
rs535956620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099152 | GGCTCACTGCAACCT[C/T]GGCCTCCTGGGTTCT | 25853 |
rs535993709 | snp | A/G/T | 0.000363541 | 0.0134781 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127315 | TCCTTTCTCCTGTCC[A/G/T]AAATGCTTCAGCCCC | 25853 |
rs536133122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119887 | TTAAATATTTTGTAG[A/G]GATGGGGTCTCACTA | 25853 |
rs536229134 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098832 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 25853 |
rs536282766 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092165 | TTTCTTCAGCCTTAT[A/T]GAGGTTTGTCATACA | 25853 |
rs536296350 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119638 | TTCTCAGGTGTGAAC[A/G]TTTTAGGCAAAAGGG | 25853 |
rs536321656 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093006 | ATGCGCCACTGCGCC[C/T]GGCTAATTTTGTATT | 25853 |
rs536346020 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114572 | CTCTCTGACAAGGGT[C/T]CAAGGATTCATGCAG | 25853 |
rs536359843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092860 | CCACACCCCTTTTTT[C/T]TTGAGACAGAATTTC | 25853 |
rs536405771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118397 | CCTCAGCCTCCCAAA[A/G]TGCCGGGATTACCGG | 25853 |
rs536563243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119233 | ATAAGAAAACGCAAG[A/G]TTCATCTAGCTGAAA | 25853 |
rs536568345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112240 | CCAATAATACTTTCT[A/G]TTCTTGGGGTTTGTG | 25853 |
rs536631615 | in-del | -/AG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121715 | TTGGGAGGCCAAGGC[-/AG]AGGCGGATCACGAGG | 25853 |
rs536693929 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112058 | TGAGACAGGAGAATT[A/G]CTTAAACTCAGGAGG | 25853 |
rs536742881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126177 | TCCTCACCGCCCTGG[A/C]CTATCTGCCCTCCAG | 25853 |
rs536749539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117798 | GCATGCCTGTAATTC[C/T]AGCTACTCGGGAGGC | 25853 |
rs536753126 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123035 | CCACCTCTACTTAAG[-/C]AGTTGAGTAAAAATA | 25853 |
rs537032258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091518 | GCGGACGCTTATAGT[A/C]CCAGCTACTCGGGAG | 25853 |
rs537091601 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090803 | GGAACTACAGGCACC[C/T]GCTACCACCCCCAGC | 25853 |
rs537094464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104464 | GGCCTTGTATGCTGT[A/G]CTATAAAATTTGTTT | 25853 |
rs537101394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121900 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 25853 |
rs537115318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098147 | ACACCAATTGAAGGG[A/G]TGGGTTTCAGAGCCT | 25853 |
rs537150077 | in-del | -/TAC | 0.0134861 | 0.0810011 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106951 | CACACTCTGATGTAT[-/TAC]TGGTAAATATTAGTT | 25853 |
rs537206755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117131 | AGGTCTTGAATTCTG[A/G]TGTTTCGCCACAGAA | 25853 |
rs537207076 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125056 | ACACACCACTTGCCT[A/G]TGATTCAACCACTGA | 25853 |
rs537313397 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086222 | ACCCAGAGCAAGCAG[A/G]TCTTAGTATTTGTGC | 25853 |
rs537331648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111389 | TGATCAAGTGCCTCT[C/T]TTGTAGGCTCCCAAG | 25853 |
rs537368646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117686 | TTGGGAGGCCCAGGC[A/G]GGAGGATCACCTGAG | 25853 |
rs537383754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126238 | CCCTGAACCCATTCC[C/T]GTTTTGCCTCTGACT | 25853 |
rs537488748 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087410 | AGACTCCCAGCTCCA[A/G]GCCCCTTAAAACCAG | 25853 |
rs537544651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120599 | TCGCTTGAACCCGGA[A/G]GCAAAGGTTACAGTG | 25853 |
rs537610867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114388 | GCCAATATGGTGAAA[C/T]CTTGTCTCTACTAAA | 25853 |
rs537731120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108689 | TACTCGGGAGGCTGA[A/G]GCAGAAGAATCGCTT | 25853 |
rs537807945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119131 | AAAAAACTCACTGTG[C/T]GACTAAGAGGAGCAA | 25853 |
rs537890723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094478 | TGCTTGTTGAATCTC[C/T]CTTATCCAAAAGGCT | 25853 |
rs538001429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121319 | ACATAGAATTTGCCC[A/G]TCGTGACAGTATCCA | 25853 |
rs538036241 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095624 | GAACTCCTGGGCTCA[A/G]GCAATCCTCCTGCTT | 25853 |
rs538173101 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099803 | TTCACCATGTTGGCC[A/G]GGCTGGTGTCGAACT | 25853 |
rs538232816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093748 | AGGCTGTTTCAACTA[C/T]TCAGGTTGTTTCTGG | 25853 |
rs538294148 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099696 | CCTCCCGGGTTCAAG[C/G]GATTCTCCTGCCTCA | 25853 |
rs538295804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093140 | AGGCGTAAGCCACCA[C/T]GCCTAGCCATCGCTC | 25853 |
rs538345538 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128101 | CAAGAGTCTGGAATC[C/T]TTTGAGAATCTCTAG | 25853 |
rs538356321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119736 | AGACAGGGTCGTGCT[C/T]TGTCACCCAGGCTAG | 25853 |
rs538363145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112856 | TAAGCTGAGATCACG[C/T]CATTGCACTCCAACC | 25853 |
rs538486255 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115546 | GGAGGTTGCAGTGAG[A/C]CGAGATAGCGCCACC | 25853 |
rs538524252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114303 | TGCGGTGGCTCACAC[C/G]TGTAATCCCAGTACT | 25853 |
rs538563567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120564 | TAGTCCCAGCTAGTC[A/G]GGGGGCTGAGGCACA | 25853 |
rs538667961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091334 | TCATCTCAACAACAA[C/T]AACAACAAAAAAGAA | 25853 |
rs538679740 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113045 | GACCAGGGATTCCCA[A/G]ACTGCTGATCAAAAT | 25853 |
rs538839260 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087923 | AGATCTCTCTCTCAC[A/G]CACACACAGACACAC | 25853 |
rs538906466 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099213 | GCTGAGATCACAGGC[A/G]CATGCTACCATGCCC | 25853 |
rs538967544 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105839 | CTGCAACCTCTGCCT[C/G]CCGGGTTCAAGCAAT | 25853 |
rs538975836 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115856 | GTGCGGGATTACAGA[C/T]ATAAGCCATCAAGCC | 25853 |
rs539101847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112350 | CCTGTAATCCCAGTA[A/C]TTTGGGAGGCCAAGG | 25853 |
rs539140656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109523 | CTTATCCACCTCCTC[C/T]GTGCACGTACGGCCC | 25853 |
rs539154032 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126930 | TCTGGCCGCCGACCT[C/G]CGACCCCAGCCCGCC | 25853 |
rs539154092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118448 | CTGAAATTGATTTCT[A/G]TATACTCAAGGATGC | 25853 |
rs539284048 | snp | A/G | 4.10139e-05 | 0.00452827 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106502 | TGTCCATCCTTGGAG[A/G]GCAGGGAGTAACAGG | 25853 |
rs539371923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122353 | CTGCCAAATCATTAA[C/T]TTCAATCCTTACTCT | 25853 |
rs539519019 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116335 | AGCCTGGGCGACAGA[A/G]AGAGTCCGTCTCAAA | 25853 |
rs539554673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100636 | AGTAGCTGTGACTAC[A/G]GGCACACCCTACCAC | 25853 |
rs539676442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096361 | CCAACTTGGGTGACA[A/G]AGTGAGACCCTGTAT | 25853 |
rs539724909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103003 | GCTGAGACAGGAGGA[C/T]TGTTTGAGACTGGGA | 25853 |
rs539796246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114037 | GGCGTGAACCTGGGA[A/G]GCGGAGCTTGCAGTG | 25853 |
rs539886789 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105893 | AGCTGGGACTACAAG[C/T]GCCCACGACCACACT | 25853 |
rs540022313 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095371 | AACCACCGCGCCAGG[C/G]CTTTTTTTTTTTTTT | 25853 |
rs540084042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094866 | ATATGTAAGGAGCTA[C/T]CTTGGGGATGGCACC | 25853 |
rs540099121 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095140 | AGTGCAGTGGCATGA[A/T]CTCGGCTCACTGCAA | 25853 |
rs540160103 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094752 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGC | 25853 |
rs540184950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120662 | GCAACACAGCAAGAC[A/G]CGGTCTCAAAAAAAA | 25853 |
rs540329335 | snp | A/G | 3.29772e-05 | 0.00406048 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093251 | ACCCATATGCAGTGC[A/G]GCTGTAGGCCTGAGG | 25853 |
rs540336358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114456 | CCTCACCCTCATTAT[C/T]GCAAAGGAATGACAA | 25853 |
rs540489235 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100499 | ACCACGCCCAGCTTC[-/T]TTTTTTTTTTTTTAA | 25853 |
rs540518724 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086919 | TTCCCCAAAATGGGA[A/T]GTTGACAGAAAAGCA | 25853 |
rs540667467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098951 | TTTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTT | 25853 |
rs540806826 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087507 | GCCTCTGGAGCTGCA[A/C]CTGGATGGTGAGTCT | 25853 |
rs540865261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091813 | AGAAATGGGATAAAG[C/T]GAGAAATGGGATAAA | 25853 |
rs540871761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093971 | TAACCCTGGGTCTTC[C/G]TCAGTTAGCAAATCC | 25853 |
rs540915529 | snp | A/C/G | 0.0166325 | 0.0896639 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091661 | AAAAAAAAAAAAAAA[A/C/G]CCACAAAAAACCCAA | 25853 |
rs540916426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120172 | TGAGCCACTGCACTT[C/T]AGCCTGGGCAACAAG | 25853 |
rs540949232 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109669 | TGGTTGTCCTGTATG[A/G]TCTGGATGAGTCCAG | 25853 |
rs541082401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091200 | GGCATGGTGGTACGC[A/G]CCTGTAGTCCCAGCT | 25853 |
rs541120419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122774 | TGAGCCACCTTGCCC[C/T]GCGAAAGAAAATCTT | 25853 |
rs541148920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099020 | AGCGATCAGCCTGCC[C/T]TGGCCTCCCAAAGTG | 25853 |
rs541149568 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096534 | GGTTGAACCCAGGAG[C/G]CAGAGGTTGCAGTGA | 25853 |
rs541157324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121826 | CAGGTACCTGTAATC[C/T]CAGCTACTCAGGAGG | 25853 |
rs541194280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123816 | TTTCTACTCCAAGTG[A/G]CAAGGATGACAGTTC | 25853 |
rs541261459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119947 | TCTGGGCTCAAGTGA[C/T]CTTCCTGTCTCAGCT | 25853 |
rs541288606 | in-del | -/TAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120083 | GGTGGGCGCCTATAA[-/TAT]TCCCAGCTACTCAAG | 25853 |
rs541295632 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114488 | GAACCACTTGAAGGA[C/T]AGAGCCACCCTGCTT | 25853 |
rs541340058 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109971 | GGGCATTACACTGGA[A/T]ACATATATAAATATT | 25853 |
rs541356974 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118625 | CAGAGACGGTAATTA[C/T]GTATCTGGTATAAGA | 25853 |
rs541466072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089235 | TGGGCCTCAGTTTTC[A/C]CACAGGCAACGTGCA | 25853 |
rs541568193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115968 | TGAACATTTATGCCA[C/T]GTCCAAATTTTTAGT | 25853 |
rs541685034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096473 | GGGCATGTTGGCAGA[C/T]GCCTGTAATCCCCGC | 25853 |
rs541725192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102602 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 25853 |
rs541773071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090948 | CAGGCATCAGCCACC[A/G]TGCCCGGCCCTATTT | 25853 |
rs541898368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095864 | CATGCCAAGTAGTCA[A/T]CAATCTATAAAGAAA | 25853 |
rs541940413 | in-del | -/G | 0.00478085 | 0.0486577 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086060 | GCAAGCACTTTCAGC[-/G]TCATTCTCAGGGCAC | 25853 |
rs541970462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102548 | ATCCCAGATACTTAG[A/G]AGGCTGAGGCAGGAG | 25853 |
rs542035583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090063 | TGTGGCAAATGCAAG[A/G]AGTCTTTTTTTATTT | 25853 |
rs542044281 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111172 | TATATTTTTACTAAA[G/T]ATGGGGTTTCACCAT | 25853 |
rs542123539 | snp | C/G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122949 | GCCAATCTGAATTTG[C/G/T]GTAAGTCTAAACCAT | 25853 |
rs542151353 | snp | A/C | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128139 | TTGGGCTGTCAGTGC[A/C]AAGAGGGGCACACTG | 25853 |
rs542155688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115803 | TTGTAATAAAACCCA[A/C]CTGGGCTCAGGCAAT | 25853 |
rs542223380 | in-del | -/A | 0.257454 | 0.249889 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111980 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAATT | 25853 |
rs542236648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094732 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 25853 |
rs542516835 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103600 | GGCTCATGCCTGTAA[C/T]CCCAGCACTTCGAGA | 25853 |
rs542538600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108962 | TCAAACAAATACATA[C/T]ATGTATTTTATGTAT | 25853 |
rs542670433 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094248 | CATCTCTACTAAAAA[C/T]ACCAAAAATTAGCTA | 25853 |
rs542727240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110128 | GAGCAGGGGGAAGAA[A/G]GGGACAAACCACTCT | 25853 |
rs542769385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117212 | TTTAAGTGACATATT[C/T]TTATAAGCTTTATAT | 25853 |
rs542919127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105484 | TATTTTAAAATGTCA[A/G]CAGTCGTTATTACTA | 25853 |
rs542938166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104665 | TCATGCCTGTAATCC[C/T]AGCATTTTAGGAGGC | 25853 |
rs543067026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117933 | AAAACAAACAAAAAA[A/G]GAAATTATTCTTGGA | 25853 |
rs543081892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097251 | GGGTGTATATTCTGA[C/T]ACTGCTTTTTTTTTT | 25853 |
rs543293871 | snp | A/T | 0.00159808 | 0.0282221 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091849 | ATAAAGAAAATACAA[A/T]TTGTTAAGTTGGATT | 25853 |
rs543305949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097382 | GCCTCAGCCTCCTGA[C/G]TAGCTGGGAATACAG | 25853 |
rs543356081 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117975 | GAACCCTATTTAGTA[A/T]TGCTTTTATATGTTT | 25853 |
rs543492218 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109852 | CAGATGTCTTAGAGA[A/G]CTTCCTTATCAATGC | 25853 |
rs543560450 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091688 | CCAAAACAAAAGCTA[C/T]TTTGCAGTATCTGCA | 25853 |
rs543568973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110081 | CAGAGAGAGAGAAAG[A/G]AGTAGCTAGAAGAGT | 25853 |
rs543586216 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123731 | TTTACAATTCAGTAA[C/T]ATTTGCTAGGCTAAA | 25853 |
rs543614619 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124607 | CTAAAAAACAGCCAA[A/G]TGTGCTATTTTAAAT | 25853 |
rs543695973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118528 | TTTCAGGTTTTTGTT[A/C]CCTGGTGACATTTCC | 25853 |
rs543725075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110847 | CCTCTACTATCATCA[C/T]CTCTTGCCATGGACT | 25853 |
rs543736341 | in-del | -/A | 0.369346 | 0.219673 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097939 | CACAGTCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 25853 |
rs543738744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111704 | GAGGGAGTTTCAGGA[C/G]AATCAGTCCAAAGGC | 25853 |
rs543852715 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128025 | GGTCAGCTTTCTTTT[C/T]TGAGTCTGTTCTAAT | 25853 |
rs543874862 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127644 | ACATTTTTGGAAGAT[C/G]CTGAAGGAATATGAC | 25853 |
rs543910100 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119690 | TTTCAACAAATACTA[C/T]GTACTTTTGCGGTTT | 25853 |
rs543927432 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109223 | CTCTCCTCCTTGGCT[A/G]TGGTATCCTGTACTC | 25853 |
rs543964409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107149 | TCTCTGACTATGGGC[A/G]GTGGGAAGTATGTGG | 25853 |
rs544086508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096608 | GACTCTGCCTCAAAA[A/G]TAAATGAATAGATAA | 25853 |
rs544123337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108219 | TCAGTCTTAGCGAAA[A/G]GACAGCCCTTAGAAG | 25853 |
rs544181664 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100132 | CTCAACTTCCTGGGC[A/C]TAAGTGATCCTCCTG | 25853 |
rs544330454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120076 | GGCTTGGTGGTGGGC[A/G]CCTATAATCCCAGCT | 25853 |
rs544480493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100831 | TTTTGTAGAGATGGA[A/G]TCTCGATTTGTTGCC | 25853 |
rs544575414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112416 | GCCTGGCCAACATGA[C/T]GAAACCATCTCTACT | 25853 |
rs544621358 | snp | C/T | 4.20787e-05 | 0.00458667 | missense | DCAF12 | GRCh38.p7 | 9:34106446 | TACCAGACACTGCCA[C/T]AGTGTCGCTGATCCA | 25853 |
rs544649879 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126600 | TAGGCGGAAAGAAAG[A/G]AAAGAGAGAGGAAGG | 25853 |
rs544667880 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086078 | ATTCTCAGGGCACCA[C/T]CCAAGCAGACAGGGC | 25853 |
rs544731527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088594 | GGAATGCTTTCTGGT[C/T]TCCTTAAGGGAACAG | 25853 |
rs544738929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105363 | CCCAGGAGTTCAAGG[A/C]TGCAGTGAGCCATGA | 25853 |
rs544760550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113138 | TCACCACAACCTCTG[A/C]CTCCTGGGTACAAGC | 25853 |
rs544778133 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122602 | CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGATTAC | 25853 |
rs544819506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099323 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 25853 |
rs544875328 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091852 | AAGAAAATACAATTT[C/G]TTAAGTTGGATTCTG | 25853 |
rs544935236 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088967 | AAAAATAAATTAGCC[A/G]GGCACAGTGCATATG | 25853 |
rs544968837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099429 | TAGAGATTGGGTTTC[A/C]CCATATTGGCCAGGC | 25853 |
rs544975349 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086561 | GTCAGTTTAAAATGA[C/T]AGAAGTTCTGTGAGA | 25853 |
rs544993253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106280 | ATTCTTGGGCTCAAG[C/T]GATCCACCCACCTCA | 25853 |
rs545052394 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125855 | AGAAGGCCTTCCCCT[C/T]CAAAGGGGGCGGCAT | 25853 |
rs545268569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107008 | TGTCACCCTCCACTA[A/G]AATGTAGGCTTCAAG | 25853 |
rs545316433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098727 | AGGTCTAGGCATTAA[A/G]ATATAACTTTTAAGT | 25853 |
rs545316522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092494 | AGATCAAGGCCATCC[C/T]GGCCAACATGGTGAA | 25853 |
rs545342582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111072 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 25853 |
rs545420094 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127382 | CGGTGCAACTTCACC[A/G]TTCCCTTTAGATTTC | 25853 |
rs545439149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108424 | AAGTCAAACATGTCA[A/C]ACCTTTACATAAATA | 25853 |
rs545484028 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123759 | AAACACTATGATGCA[C/T]GTGCGGGGAGTGGAA | 25853 |
rs545508542 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102341 | TTAAAAAGATAAATC[A/C]GTTTTCTTAGCAAAC | 25853 |
rs545624284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105278 | AAAAATCATACTAAG[C/G]CTGGGTGCAGTGGCT | 25853 |
rs545634572 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094143 | GGCGTGGTGGCTAAC[A/G/T]TCTGTAATCCCAGCA | 25853 |
rs545711308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095798 | TATCTTAATTTGATC[A/G]ATCTTCAATTGCCAA | 25853 |
rs545865370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101657 | TCAGCCTCCCAAAGT[A/G]CAAGGATTACAGGCA | 25853 |
rs545904177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108859 | AAGGTGGCAAGTGCC[G/T]GTAGTCCCAACTACT | 25853 |
rs546130218 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107958 | AGAAACTTTTAAACG[-/A]AACACAATTCCCAGA | 25853 |
rs546278383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094673 | GTAGCTGGGACTACA[A/G]GCGCCCACCACCACG | 25853 |
rs546286200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100285 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG | 25853 |
rs546298329 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099586 | CTAATTTTCTTTTTT[A/C]TTTTTCTTTTTTTTC | 25853 |
rs546308664 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102401 | GGCACGGTGGCTCAC[A/G]CCTGTAACCCCAGAA | 25853 |
rs546339467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094016 | CAACACATAAGACAG[C/T]ATACAAGGTCAGTGG | 25853 |
rs546374737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093653 | GGTAAGACCTAGATA[A/C]TGAAGGAGATAGGTT | 25853 |
rs546424707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109463 | CTTGTGGGGGATTCA[A/G]TGAACAAAGTAGCTG | 25853 |
rs546425046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094181 | AGGCTAAGGCAGGCA[C/G]ATCACCTGAGGTCAG | 25853 |
rs546466403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088545 | ACAATTAGCACCTCT[A/G]GCCATGGGGCAGGAA | 25853 |
rs546487078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099377 | GCTGGGACTACAGGC[A/G]CGTGCCACCACGCCC | 25853 |
rs546515587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114660 | CAGAAACTAGCAGCG[C/T]GGCAAGGTAAGCTCG | 25853 |
rs546517281 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121620 | TGCCATCCTTCTCCT[A/C]AAATCACACCCCACC | 25853 |
rs546529457 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128619 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 25853 |
rs546712388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092662 | CTACACTCCAGCCTG[A/G]CAAAAGAGCGAGACT | 25853 |
rs546868535 | in-del | -/A | 0.262985 | 0.249663 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115598 | GCAAGACTTCGTCTC[-/A]AAAAAAAAAAAGTAT | 25853 |
rs547006000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123701 | ACAAGCAAGAGGCTA[C/T]GATGATTAATTCAGT | 25853 |
rs547095129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093007 | TGCGCCACTGCGCCC[A/G]GCTAATTTTGTATTT | 25853 |
rs547158626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126187 | CCTGGCCTATCTGCC[C/T]TCCAGTTAACGAGGG | 25853 |
rs547196439 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090129 | AGTGCAATGGCGCGA[A/T]CTTGGCTCGCTGCAA | 25853 |
rs547264124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113402 | AGCTCTGTCACCCAA[A/G]CTGGAATGCAGTGGC | 25853 |
rs547347804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119559 | TAAGTATTCGATTGT[C/T]AGTATTTAGATTAAG | 25853 |
rs547402313 | snp | C/G | 1.64833e-05 | 0.00287078 | missense | DCAF12 | GRCh38.p7 | 9:34089505 | CTCTTCCAGAAATCT[C/G]TGAGCTCGGATGTCA | 25853 |
rs547404845 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108658 | GGGCATGGTGGCACA[C/T]GCCTGTAATCTCAGC | 25853 |
rs547440086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114194 | ACAACATGGATGAAC[C/G]TAGAGGACATTATGT | 25853 |
rs547561326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122134 | ACCATTTTTGGCTCA[C/T]AGTACTCTCTTTCAA | 25853 |
rs547595322 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113487 | TGGGATGGCAGGTGC[A/T]CACCACTGTGCCCAG | 25853 |
rs547618062 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100792 | GGTATGAGCCACCAA[A/C/G]CCTAGCCTTATTTTT | 25853 |
rs547622577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123040 | TCTACTTAAGCAGTT[G/T]AGTAAAAATATGACT | 25853 |
rs547627680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097762 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 25853 |
rs547629311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109100 | ACACACAGACATGGC[C/T]ATCACAGAACAGACT | 25853 |
rs547664055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102950 | AGGCATGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 25853 |
rs547702464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109832 | GCAGCTTTAGGGGTC[A/G]GAAGCAGATGTCTTA | 25853 |
rs547743693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116941 | CCGAGATCGTGCCCC[C/T]ACACTCCAGCCTGGG | 25853 |
rs547862176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108589 | CAGAGCTTGAGAGTT[C/T]GAGATCAGCCTGGCT | 25853 |
rs547898715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114777 | TGTATCTAGACAAAT[A/G]TAAATGAGTGTACAC | 25853 |
rs547981996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095253 | CTAATTTTTGTATTT[C/T]TAGTAGAGACGGGGT | 25853 |
rs548070443 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109355 | ACTGTACGAGATGCA[A/C/T]CTGAACAGCTCCTAG | 25853 |
rs548104828 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095363 | TAGGCGTGAACCACC[A/G]CGCCAGGCCTTTTTT | 25853 |
rs548116931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094825 | GTGAGCCACCGCACC[C/T]GGCCCCGATTTTTAA | 25853 |
rs548131767 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094805 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 25853 |
rs548144608 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128497 | ATCTCGGCTCACTGC[A/C]GGCTCCGCCTCCTGG | 25853 |
rs548178697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116213 | AATATAAAAATTAGC[C/T]GGGCATGGTGGCAGT | 25853 |
rs548214220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122909 | GCAAACTTTTCTTCA[C/T]TTAGCTTTTCTGTCT | 25853 |
rs548254446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119763 | CTAGAGTGCAGTGGT[A/G]TAATCCCATTTAACT | 25853 |
rs548294655 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128009 | GAGTGGGTCAGGAGT[C/G]GGTCAGCTTTCTTTT | 25853 |
rs548329193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122023 | CCCGGTTTTCCTGAG[C/T]TCCCTGCTCCCCCGC | 25853 |
rs548489021 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115432 | CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC | 25853 |
rs548575617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123981 | CAACCACCATGGTAT[C/T]ATTTCCTTCCTCAAA | 25853 |
rs548599052 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096070 | TCTTTTAAACAAGAA[C/T]TGAGACCAGGTGCAA | 25853 |
rs548628111 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087564 | TAAGCAGATGTGAGG[C/G]TGGGAAGGGGAAGTG | 25853 |
rs548690453 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120441 | TTTGGGAGGCTGAGG[C/G]GGGCAGATTACATGA | 25853 |
rs548725965 | in-del | -/T | 0.0402882 | 0.136092 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090674 | ATTTAGTCTTTTCTC[-/T]TTTTTTTTTGAGCTC | 25853 |
rs548794527 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090167 | CTTCCGGGTTCAAGC[A/G]ATTCTCCTGCCTTAG | 25853 |
rs548794625 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114146 | TACACAATGCAATAC[C/T]GTTTAGCTATAAAAA | 25853 |
rs548830871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117439 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCTCTAA | 25853 |
rs548864967 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124627 | CTATTTTAAATACTT[C/T]GACATACGTTCTTAG | 25853 |
rs548898903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101133 | CTGGAGTGCAATAAC[A/G]TGATTATGGCTCATT | 25853 |
rs548915894 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109758 | GGAAGCTCAGGCAGG[G/T]GGTGACCCCACTCAC | 25853 |
rs548932282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117038 | ATCTTAGACACTCTG[A/C]GCTGTGAATCTAAAC | 25853 |
rs548935708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108562 | TTTAGGAGGCCAAGG[A/C]GGGCGGATCACCAGA | 25853 |
rs549079249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102813 | GGGCGCAGTGGCTCA[C/T]GACTGTAATCGCAAC | 25853 |
rs549152327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104272 | AAAATTAAAAAAAAA[G/T]AAAAAAACATCTAAA | 25853 |
rs549591028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090266 | ACAGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 25853 |
rs549736320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123347 | CTAGTACTTTTAAAT[A/G]AGTAAGATATTGCTC | 25853 |
rs549738692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115330 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 25853 |
rs549797221 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092840 | CCCTTTTGTGTCACT[-/C]CCCCCCACACCCCTT | 25853 |
rs549830854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091271 | GGCAGAGGGTGCAGT[G/T]AGCTGAGATCACACC | 25853 |
rs549919604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121888 | GCAGAGGTTGCAGTG[A/G]GCTGAGATCGCGCCA | 25853 |
rs549974064 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110392 | ATATTCTTACAGCTG[A/C]CTCCTTCCTCTGCTT | 25853 |
rs549976154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117402 | TGATCTGCCTGCCTC[A/G]GCCGGCCAAAGTGCT | 25853 |
rs550065091 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102795 | AATGTTATATTCCTG[A/G]CTGGGCGCAGTGGCT | 25853 |
rs550084831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103706 | AAAAAATAGAAATAA[C/T]TAACCGGGTGTGGTG | 25853 |
rs550134466 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111130 | AGCTGGGACTACAGG[C/T]GTGCACCACCACGCC | 25853 |
rs550172200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112075 | TTAAACTCAGGAGGT[A/G]GAGGTTGCAGTGAGC | 25853 |
rs550212341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095999 | GCAAGAGAGGCACAC[C/T]AGACTCAAAATTTCA | 25853 |
rs550259873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106359 | GGCTGTTTCCTATCA[C/T]ACTACTATCCCTTTT | 25853 |
rs550314898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095430 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGGCAAAA | 25853 |
rs550486566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090188 | CCTGCCTTAGCCTCC[C/T]AAGTAGCTGGGATTA | 25853 |
rs550665827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097521 | TCGGCCTCCGAAAGT[A/G]CAGGGATTACAGGCG | 25853 |
rs550909582 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116893 | ATGAGGCAGAAGAAT[C/G]GCTTGAACCCAAGAG | 25853 |
rs550933176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118292 | GCATGCGGCATCATG[C/T]CCGGCTAATTTTTGT | 25853 |
rs550970052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125993 | ACGCAATCATCCCAG[C/T]TTCCTAGGGCCCATG | 25853 |
rs551056584 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108076 | CTCATGGCTGTTCTC[C/T]ATACACACACATCCC | 25853 |
rs551305007 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126729 | CCCTTGCTCGCGCGC[C/T]GTCACCCTTGCGCAG | 25853 |
rs551325677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111372 | TCTCTAAATGTCCAG[G/T]CTGATCAAGTGCCTC | 25853 |
rs551441765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103642 | GAGGATCGCTTGAGC[A/C]TAGGAGTTTGACAGC | 25853 |
rs551456807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097482 | AGGCTAGTCTCAAAC[A/T]CCTGACCTTGTGATC | 25853 |
rs551590852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091959 | CTATGTTTTCTCATC[C/T]GCTTCCCACAGGGTT | 25853 |
rs551612485 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111735 | TAGATTGGACTAGGC[C/T]ATTCAGATTCTTTAG | 25853 |
rs551707248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099007 | ACTCCTGAGTTCCAG[C/T]GATCAGCCTGCCTTG | 25853 |
rs551845915 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087967 | TTTCACAGAAAGTCT[A/G]AGAGCAACCATGTAA | 25853 |
rs551847867 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094767 | AATCTCCTGACCTTG[C/T]GATCCGCCCACCTTG | 25853 |
rs551861886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094237 | TGGTGAGATGCCATC[G/T]CTACTAAAAATACCA | 25853 |
rs551875479 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087074 | AGACAGTTCAAGGGA[A/G]GAACAGACAAATTAC | 25853 |
rs552108969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100389 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 25853 |
rs552210838 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100559 | GAGTGGAGTGGTGCA[A/G]TCTCAGCTCATCCCA | 25853 |
rs552269532 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126954 | GCCCGCCTATCCGCA[A/G]GCACCCGGAAGTGAG | 25853 |
rs552272395 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121204 | ACTGACTAAACCACA[A/C]AAAGATCAAACATCC | 25853 |
rs552322394 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086097 | AGCAGACAGGGCCTA[C/T]TACCAACCCTTACTT | 25853 |
rs552408166 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123795 | TCTTCCAAGCAGGAG[A/G]CTCTTTTTCTACTCC | 25853 |
rs552521968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099170 | CCTCCTGGGTTCTAG[C/T]GATTCTCCTGCCTCA | 25853 |
rs552554101 | snp | A/C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107118 | TGAATGAATGGATGA[A/C/T]TTAGTAAACTGCTAC | 25853 |
rs552627196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106577 | AACTCTCTAAAGAAG[C/G]ATACAAGTCAGACTG | 25853 |
rs552633847 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088855 | TGGTTCATGGCTGTA[A/C]TCCCAGAATTTTAGG | 25853 |
rs552748397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119071 | ATGGTTGTGTATTTG[C/T]CCATTGAGAATCAAG | 25853 |
rs552859296 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105279 | AAAATCATACTAAGG[C/T]TGGGTGCAGTGGCTC | 25853 |
rs552890323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119941 | TGAATCTCTGGGCTC[A/G]AGTGATCTTCCTGTC | 25853 |
rs552936090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114104 | CAGGGCAAATACTCC[A/G]TCTCAAAAAAAAAAA | 25853 |
rs553026885 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086536 | GAAGATTTTTTTTTT[A/T]AATATACAAGTCAGT | 25853 |
rs553037691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112977 | ACAAAATTAATTGCC[A/C]ACTCACATATTTGTG | 25853 |
rs553040857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093127 | GTGCTGGGATTACAG[A/G]CGTAAGCCACCACGC | 25853 |
rs553169440 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125992 | GACGCAATCATCCCA[A/G]CTTCCTAGGGCCCAT | 25853 |
rs553280617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105260 | TCTGTCTCAAAAAAA[A/G]AAAAAAATCATACTA | 25853 |
rs553419912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124407 | TGGTTACAAAGCTTA[C/T]TGAGAAATTTTTCAC | 25853 |
rs553535565 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118427 | GAGTGAGCCACTGCC[C/T]CCGGCCTGAAATTGA | 25853 |
rs553620189 | in-del | -/A | 0.400504 | 0.199621 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114108 | CAAATACTCCGTCTC[-/A]AAAAAAAAAAATGTG | 25853 |
rs553632467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095739 | TTGTATTGTAAATTA[A/C]GTCTATTTTCTCATT | 25853 |
rs553656518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109451 | AGCTGTTTTCACCTT[A/G]TGGGGGATTCAATGA | 25853 |
rs553718282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117680 | AGCACTTTGGGAGGC[C/T]CAGGCGGGAGGATCA | 25853 |
rs553913689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113174 | TCCTGCCTCAGCCTC[A/G]CCGAGTACCTGGGAT | 25853 |
rs554003355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108099 | CACATCCCATTCAGT[A/C]CTATTCCTCCCTGCC | 25853 |
rs554051217 | in-del | -/T | 0.252702 | 0.249985 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100669 | TGGCTAATTTTTGCA[-/T]TTTTTTTTTTTTTAT | 25853 |
rs554051353 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119575 | AGTATTTAGATTAAG[C/T]AGCTTCCAATTATTA | 25853 |
rs554141638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113783 | GATACGGAATCAGCC[A/G]AAGTGTGCATCAGTG | 25853 |
rs554167016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088866 | TGTAATCCCAGAATT[G/T]TAGGAGGCCAAGGTG | 25853 |
rs554169645 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092684 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAACAA | 25853 |
rs554179852 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088215 | TTCTTCCTATTAAGT[A/G]CCTAAACTATAGGCA | 25853 |
rs554350790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099867 | AAAGTGCTGGGATTA[C/T]AGGCATAAGCCAGTG | 25853 |
rs554381767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094592 | CTGGAGTACAGTGGC[A/G]CGATCTCAGCTCACT | 25853 |
rs554430906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115047 | AAGGGTGTTTCAGAC[C/T]GGAGCCCAATGAGAA | 25853 |
rs554433462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101496 | TTACTGGGTTCAAGT[A/G]ATTCTCCTACCTCAG | 25853 |
rs554467745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121363 | GCTATATCCTTAAGC[C/T]GTCCCCCAAATCACG | 25853 |
rs554470108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108714 | TCGCTTGAACCGAGG[A/C]GGCGGAGGTTGCAGT | 25853 |
rs554618377 | snp | C/T | 0.0205511 | 0.0992634 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128257 | CGCGATTTCTTTTCT[C/T]TTTTTTTTTTTGAGA | 25853 |
rs554704980 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093059 | CATATTTATTGGTCA[A/G]GCTGATCTCAAACTC | 25853 |
rs554731968 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120502 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 25853 |
rs554751484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099325 | CACTGCAACCTCCGC[C/G]TCCCAGGTTCAAGCG | 25853 |
rs554840202 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087425 | GGCCCCTTAAAACCA[C/G]ATCAGGTCTTGAGGG | 25853 |
rs554963822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094580 | CTGTCGCCCAGGCTG[C/G]AGTACAGTGGCGCGA | 25853 |
rs555089553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106831 | TCCTTTAAGTCTCCC[C/T]GCTCAAGCGTCATCC | 25853 |
rs555119563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099814 | GGCCAGGCTGGTGTC[A/G]AACTCCTGACCTCAT | 25853 |
rs555126353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113696 | AAACAATTCCCAGGC[C/T]TTACCCTAAAACTCT | 25853 |
rs555235080 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087458 | AGGAGAGAGAAGCTA[C/G]GATGGGGATTCAAGT | 25853 |
rs555384547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091596 | TGAACTGAGATTGCA[C/G]CACTTTCCTCCAGCC | 25853 |
rs555424438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096477 | ATGTTGGCAGACGCC[C/T]GTAATCCCCGCAGCT | 25853 |
rs555468685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110513 | TCAACTTCCTAAAAA[C/T]GGAAATCTTCCCATG | 25853 |
rs555492378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103818 | TGCACTCCAGCCTAC[A/G]TAACAGAGTGAGACC | 25853 |
rs555530293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103184 | TAGGAGGCCGAGGCA[A/G]GTGGATCACGAGGTC | 25853 |
rs555552823 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114230 | GAAACAAGCCAAGTA[C/T]AGAATACTGAATGAC | 25853 |
rs555573297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097011 | GGTTGAAAAACTCCT[C/T]ACTATGCTATCACTC | 25853 |
rs555576565 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089738 | ACAGTGTTTTCCCAA[C/T]GGCAAGTTAGCTCAT | 25853 |
rs555634060 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092218 | AATTTGAGGTTCTGA[C/G]ATATGTATATATCCA | 25853 |
rs555682825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123476 | TTTGCCCAATGTCAC[A/G]AAGTTCAGAGAAGAG | 25853 |
rs555839877 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089157 | AGCTGTGGTGGGAGG[C/T]CCCTTATCCTTCTTG | 25853 |
rs555888052 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114973 | CCTTGCCTCTAAAAA[C/G]AAAAAACACAAAAAC | 25853 |
rs556058033 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103052 | CCATGATCACATCAC[A/G]CCACTGCATTCCATC | 25853 |
rs556110221 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092846 | TTGTGTCACTCCCCC[C/G]ACACCCCTTTTTTTT | 25853 |
rs556223314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096402 | TAAAAATAAAAATAC[C/T]AACCTGGCCAACATG | 25853 |
rs556258033 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108669 | CACACGCCTGTAATC[C/T]CAGCTACTCGGGAGG | 25853 |
rs556342918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109524 | TTATCCACCTCCTCC[A/G]TGCACGTACGGCCCC | 25853 |
rs556417566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101377 | TGTGCCCGGCCATAA[C/T]TCCTTTATTATTTAT | 25853 |
rs556425449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090804 | GAACTACAGGCACCC[A/G]CTACCACCCCCAGCT | 25853 |
rs556590515 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115896 | CATACCTTTAACGGC[A/G]ATAAGGTAGTTCACT | 25853 |
rs556734384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094685 | ACAAGCGCCCACCAC[C/T]ACGCCCGGCTAATTT | 25853 |
rs556759148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088931 | CCTGGGCAACATGGC[A/G]AGACCCCATCTCTAC | 25853 |
rs556856411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121642 | CACCCCACCCCCAGC[C/T]CCTTCAAGAGCCCTC | 25853 |
rs556901253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091523 | CGCTTATAGTCCCAG[C/T]TACTCGGGAGGCTGA | 25853 |
rs556994260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092789 | AACAAAGGCTTCTGT[A/G]GCCACACATTTGTCT | 25853 |
rs557198957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103994 | AACATCTAGGCCAGG[C/T]GCAGTGGCTCACGCC | 25853 |
rs557258646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111393 | CAAGTGCCTCTCTTG[C/T]AGGCTCCCAAGATAT | 25853 |
rs557275945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117154 | CCACAGAATCATGAC[C/T]TCGTGGAAGGAGGGC | 25853 |
rs557296007 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086346 | TCATGTGGGGCCTTT[C/T]TGGCAGGCTCCTGGC | 25853 |
rs557413687 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111078 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 25853 |
rs557439581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103865 | AACAGTAACAACAAC[A/G]ACGAAAATGTGTTTT | 25853 |
rs557476656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110752 | TGGTGCCACTGCACT[C/T]GCACCTGGGTGACAG | 25853 |
rs557495157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117696 | CAGGCGGGAGGATCA[C/T]CTGAGGTTGGGATTT | 25853 |
rs557527568 | snp | A/G | 3.42395e-05 | 0.00413746 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107578 | TAGCTACAAGAAAAA[A/G]TGGATACAGAAGCTG | 25853 |
rs557700174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096329 | GGCTGCACTGATCCA[A/T]GAGCCATGACTGCAC | 25853 |
rs557729848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125535 | TGCAGAATAGAACAG[A/C]CTAAAAGGTTTACTA | 25853 |
rs557837297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090599 | ATGAAAGTTACCCCC[A/G]TTAAACAGTACCAAA | 25853 |
rs557865168 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091671 | AAAAAACCACAAAAA[A/C]CCCAAAACAAAAGCT | 25853 |
rs557867101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097745 | CAAGACCAGCCTGGC[C/T]AACATGGTGAAACCC | 25853 |
rs557913012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124215 | ATTATGACATTACTT[A/G]TCCATTCACACAGGG | 25853 |
rs557914665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116721 | GCACGGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 25853 |
rs558039099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105831 | TCAGCTCACTGCAAC[C/T]TCTGCCTGCCGGGTT | 25853 |
rs558074645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117067 | ACTGTTCCTACACAA[G/T]ATGGACTACACTACT | 25853 |
rs558095461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093854 | GATAAAGAGGCTGAT[A/C]TCTGGCTACCCCCAG | 25853 |
rs558176926 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090427 | CCCAGAACTTAAATA[C/G]CCAAAGATGTTTAAG | 25853 |
rs558265416 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127476 | CTTATCTGTAGCTGC[A/C]TGCCTCACTCTTGGA | 25853 |
rs558316245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120592 | ACAAGAATCGCTTGA[A/C]CCCGGAGGCAAAGGT | 25853 |
rs558352932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120059 | AACAAAAAAATTAGC[C/T]GGGCTTGGTGGTGGG | 25853 |
rs558472413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114333 | TTTGGGAGTCTGAGG[C/G]TGGTGGATCACCTGA | 25853 |
rs558474260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109993 | ATAAATATTTAAATT[A/T]TATATAATTATATAT | 25853 |
rs558717225 | in-del | -/TA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103440 | AATAAAAAGTAAGTT[-/TA]TATATTCCCATTCAG | 25853 |
rs558804395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093188 | TCCAAATGTTCCATA[C/T]AGAGCACTATACCTG | 25853 |
rs558891054 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095885 | TATAAAGAAATACTT[A/C]AATGCATTGTTGAGG | 25853 |
rs558918189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125769 | GCGCTCCAGGCAGTT[A/G]CAGAATTCGAAAAAT | 25853 |
rs558981323 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126595 | AAAGATAGGCGGAAA[A/G]AAAGGAAAGAGAGAG | 25853 |
rs559017119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117986 | AGTATTGCTTTTATA[C/T]GTTTACAAATCCCAT | 25853 |
rs559079761 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105907 | GCGCCCACGACCACA[C/G]TCAGCTAATTTTTTG | 25853 |
rs559104916 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122036 | AGTTCCCTGCTCCCC[C/T]GCAGCAGTTCTTCTT | 25853 |
rs559141816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118267 | GACTCCCGAGTAGCC[A/G]GGACCACAGGCATGC | 25853 |
rs559142583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112363 | TACTTTGGGAGGCCA[A/C]GGCAGGCGGATCACC | 25853 |
rs559174258 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118867 | TACTTGGTGGTGCTG[A/G]AGCAGAAGAATCGCT | 25853 |
rs559202816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112813 | TGAGGCAGGTGAATC[A/G]CTTGAACCCGGGAGG | 25853 |
rs559243776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099216 | GAGATCACAGGCGCA[C/T]GCTACCATGCCCTGC | 25853 |
rs559306593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111752 | TTCAGATTCTTTAGG[A/G]AATATGTAACTGGCT | 25853 |
rs559463895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103634 | TCAAGTGGGAGGATC[A/G]CTTGAGCCTAGGAGT | 25853 |
rs559477961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097398 | TAGCTGGGAATACAG[C/G]CATATGCCACCATGC | 25853 |
rs559527081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103963 | CTGCTAATCTCCTGA[A/G]CACTTCATAGAAAAA | 25853 |
rs559643421 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127835 | TCAAGTTCTGTCAAC[A/G]AGGAGATTTGGATTT | 25853 |
rs559664934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098001 | GTTTTCAGAAGCAAG[C/T]ATGAAAATCATGCCC | 25853 |
rs559678027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117273 | TTTTTTTTTTTTTGA[A/G]ATGGAGCTCAAAAAA | 25853 |
rs559728255 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120124 | AGGAGAATCACTTCA[A/G]CCTGGGAGGCGGAGG | 25853 |
rs559840228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111024 | CAAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 25853 |
rs559840707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091890 | GCTGTTCCCCCATCA[A/G]GCTGTGTGATGCTGG | 25853 |
rs559869865 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094765 | TCAATCTCCTGACCT[C/T]GCGATCCGCCCACCT | 25853 |
rs559874656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114470 | TTGCAAAGGAATGAC[A/T]ATGAACCACTTGAAG | 25853 |
rs560058454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095169 | AACCTCTGCCTCCTG[A/G]GTTCAAGCGATTCTC | 25853 |
rs560077714 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107389 | AGGATCCAGCGTAGG[C/T]AGTCGATAGATGGCA | 25853 |
rs560233284 | in-del | -/C | 0.00024325 | 0.0110257 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127223 | AACCAACCCAGGCCG[-/C]CCTACGAGTCTCTGG | 25853 |
rs560292913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106065 | TATTTTAAAATTTTC[C/T]TACAATAAATGTGTA | 25853 |
rs560362682 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092581 | GTCCCACCTACTCGC[C/G]AGGCTGAGGCAGGAG | 25853 |
rs560494899 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098975 | GGGTTTTACCATGTT[A/G]CCCAAGCTGGTCTTG | 25853 |
rs560503786 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093565 | CCACATAAAATCAAG[C/T]CCTGATTACAGAAAT | 25853 |
rs560614433 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086946 | AGCAGAGTATGTGCT[C/T]AGAGGAACTGGTGGG | 25853 |
rs560667967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119636 | AATTCTCAGGTGTGA[A/C]CATTTTAGGCAAAAG | 25853 |
rs560668040 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128310 | GGCTGGAGTGCAGTG[C/G]CACGATCTCGGCTCA | 25853 |
rs560691606 | snp | A/T | 5.75705e-05 | 0.00536488 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106402 | CCCAATCCCTGCCAC[A/T]TCAAAAGCTCCCTAT | 25853 |
rs560703295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120130 | ATCACTTCAACCTGG[A/G]AGGCGGAGGTTGCAG | 25853 |
rs560708105 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100215 | TTTTTTTTTTTTTTT[C/T]TGAGATGGAGTCTCA | 25853 |
rs560723513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120290 | GATTCTGGGGCAGGA[A/G]GATCCCTTGGGCCCA | 25853 |
rs560747785 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092036 | TCAAAGTACACTAAA[A/G]TAAGTATTTTTTCCC | 25853 |
rs560876218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100834 | TGTAGAGATGGAGTC[C/T]CGATTTGTTGCCAAG | 25853 |
rs560918319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113327 | AAAGTGCTGGGATTA[C/T]AGGCATGGGCCACTG | 25853 |
rs560957357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119553 | TTTACTTAAGTATTC[A/G]ATTGTTAGTATTTAG | 25853 |
rs561010862 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114310 | GCTCACACCTGTAAT[A/C]CCAGTACTTTGGGAG | 25853 |
rs561074332 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104666 | CATGCCTGTAATCCC[A/C]GCATTTTAGGAGGCC | 25853 |
rs561086260 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094414 | TGTCTCAAAAAAAAT[-/A]AAAAAAAAGACAAAT | 25853 |
rs561269174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104849 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 25853 |
rs561282193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094137 | AAGCTGGGCGTGGTG[A/G]CTAACGTCTGTAATC | 25853 |
rs561298441 | snp | A/G | 0.000313265 | 0.0125114 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093249 | GAACCCATATGCAGT[A/G]CAGCTGTAGGCCTGA | 25853 |
rs561480680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098822 | CACCCAGGCTGGAGT[A/G]CAGTGGTGCGATCTC | 25853 |
rs561520154 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127648 | TTTTGGAAGATCCTG[A/G]AGGAATATGACTGCC | 25853 |
rs561670828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109584 | CAGAGGGGGGTCCCA[C/T]GCAGCCATCATATTC | 25853 |
rs561672626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101898 | GGGCACGCCTGTGGT[C/T]CCAGCTACTCAGGAG | 25853 |
rs561678316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095892 | AAATACTTAAATGCA[C/T]TGTTGAGGAGGACTG | 25853 |
rs561683339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095273 | AGAGACGGGGTTTCG[C/T]CATGTTGGCCAGCAT | 25853 |
rs561859499 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122913 | ACTTTTCTTCACTTA[C/G]CTTTTCTGTCTGGCT | 25853 |
rs561892824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090953 | ATCAGCCACCGTGCC[C/T]GGCCCTATTTATTCC | 25853 |
rs561907556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088596 | AATGCTTTCTGGTCT[C/T]CTTAAGGGAACAGGG | 25853 |
rs562120524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115147 | GGGCAACCTAAGTCT[A/G]TGGAGAGGTTGGGAA | 25853 |
rs562161204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34121742 | GAGGTCAGAAGATCG[A/C]GACCATCCTGGCCAA | 25853 |
rs562236806 | in-del | -/C | 0.00478085 | 0.0486577 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086062 | AAGCACTTTCAGCGT[-/C]ATTCTCAGGGCACCA | 25853 |
rs562406577 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111840 | GAAAAGAAAACTTGA[A/G]ACTTGAAGCATGGGC | 25853 |
rs562408396 | snp | A/C | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086081 | CTCAGGGCACCATCC[A/C]AGCAGACAGGGCCTA | 25853 |
rs562412480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109043 | AATGGTTTCATTGGA[G/T]TGTCTTTAGAGCTGT | 25853 |
rs562480747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089976 | CAACCTACACTGCAA[C/G]TCAAGGTAATCTGCA | 25853 |
rs562653287 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094773 | CTGACCTTGCGATCC[A/G]CCCACCTTGGCCTCC | 25853 |
rs562709446 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089044 | AGCCCAGGAGTTCAA[C/G]GCTACATACAGTAAG | 25853 |
rs562821598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094029 | AGCATACAAGGTCAG[A/T]GGAGCTCAAAGGCTA | 25853 |
rs562823612 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087055 | TAAAAACCTCAGACT[A/G]AACAGACAGTTCAAG | 25853 |
rs562824421 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112209 | TTCAATTCCTGTTTC[C/T]ACTTCTCTCTGAGAT | 25853 |
rs562948986 | snp | C/G | 0.000346258 | 0.0131533 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088553 | CACCTCTAGCCATGG[C/G]GCAGGAAAAGGGGGA | 25853 |
rs562954983 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128394 | TAGCTCAGATTACAG[A/G]TGCTCGCCACGTTGC | 25853 |
rs563008500 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087537 | TGATGTTTTAGGGGT[A/G]TGGCTACTGGCTAAG | 25853 |
rs563026440 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099785 | TTTTAGTAGAGACGG[C/T]GTTTCACCATGTTGG | 25853 |
rs563192409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124662 | TTTTCACTATTATGT[A/G]TCCTGAATGATGCTC | 25853 |
rs563208344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092186 | TTGTCATACAATATA[C/T]GACACATAAAGTATA | 25853 |
rs563247193 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100531 | ACAAGGCCTCACTCT[G/T]TTGCCCAGGCTGGAG | 25853 |
rs563317877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116091 | ATCCAGGGCTGGGTG[C/T]GGTGGCTCACGCCTG | 25853 |
rs563445746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102099 | GCACTCTGGGAGACC[A/G]GGTAACATGGCAAAA | 25853 |
rs563474097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118166 | AAAAAGACAGACTCA[C/T]TCTGTCGCCCAGGCT | 25853 |
rs563510455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125692 | CAGTCCAAGGAGCCA[C/G]ACCTGGCTCCCAGGT | 25853 |
rs563540135 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110082 | AGAGAGAGAGAAAGG[A/C]GTAGCTAGAAGAGTG | 25853 |
rs563677159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123752 | CTAGGCTAAACACTA[A/T]GATGCACGTGCGGGG | 25853 |
rs563698057 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110469 | CTTCAGGCAACACCG[C/T]TATCAAAATTATTCT | 25853 |
rs563704724 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106581 | CTCTAAAGAAGCATA[C/T]AAGTCAGACTGAAAA | 25853 |
rs563897642 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104865 | GGAGGTTGCAGTGAG[C/T]CAAGATTGCACCATT | 25853 |
rs563959835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091295 | TCACACCACTCCACT[A/C]CAGCCTAGGTGACAG | 25853 |
rs563995675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097317 | CCCAGGCTGGAGTGC[C/T]GTGGCGCAATTTCGG | 25853 |
rs564025168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096590 | GCCTGGGCATCAGAG[C/T]GAGACTCTGCCTCAA | 25853 |
rs564057302 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128184 | CTCTTTCTCAAAGTT[C/T]CTTTACTTCATCTTC | 25853 |
rs564086564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095972 | CTGTCTTACTCTTTA[A/G]AAGACTTTCCTGCAA | 25853 |
rs564117846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103322 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 25853 |
rs564210970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091222 | GTCCCAGCTACTCAG[A/G]AGGCTAAGGCAGGAG | 25853 |
rs564272067 | snp | A/G | 0 | 0 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124581 | GTTTATACATTTTTA[A/G]ATTCTGTTCACTAAA | 25853 |
rs564308955 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123819 | CTACTCCAAGTGACA[A/G]GGATGACAGTTCTTA | 25853 |
rs564364463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116017 | GAACATTCTTTTATT[A/G]AAATCCAGGGCCTCC | 25853 |
rs564508580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109659 | TCAGTACTGCTGGTT[G/T]TCCTGTATGGTCTGG | 25853 |
rs564599565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112562 | TCACACCACTGCACT[C/T]CAGCCTGGGCGACAG | 25853 |
rs564725209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109103 | CACAGACATGGCTAT[C/T]ACAGAACAGACTATG | 25853 |
rs564911076 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126673 | TTCCGACGGCAGAGC[A/C]TGCAAGGACGGCGAG | 25853 |
rs564945971 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104272 | AAATTAAAAAAAAAG[-/A]AAAAAAACATCTAAA | 25853 |
rs564957231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105691 | AGTGGTTATCTCTGG[A/T]TAGAGATCTTGTGGG | 25853 |
rs565015364 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094720 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 25853 |
rs565060812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097202 | TTCAAACTGTGGCCT[C/G]ATTCAGATTCTGGAG | 25853 |
rs565065249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097507 | GTGATCTGCCTGCCT[C/T]GGCCTCCGAAAGTGC | 25853 |
rs565077030 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106303 | CCACCTCAGCCTCCC[A/C]AAGTGCTGGGATTAT | 25853 |
rs565077907 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116562 | TACCTGTAGTCCCAG[C/T]TACTTGGGAGGCTGA | 25853 |
rs565210505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099514 | TGGGATTACAGGCAT[A/G]AGCCACCGCGCCTTA | 25853 |
rs565264975 | in-del | -/A | 0.413083 | 0.189483 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120203 | ATGAAAGTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs565276438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092960 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGCA | 25853 |
rs565368441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124902 | ACGGGAAAGAATGGA[A/G]AGGAGAGTAAGGCAA | 25853 |
rs565425637 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104776 | ACAAAAATTAGCCAG[C/G]CGTGGTGGTGGGCAC | 25853 |
rs565447799 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122816 | GCTCAAATTCCTACA[C/T]GGCAACAGTTGGTTA | 25853 |
rs565534627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110564 | ATCCAATGACTCCCC[A/G]TCACCTAAATCTGAG | 25853 |
rs565571422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117050 | CTGAGCTGTGAATCT[A/T]AACTGTTCCTACACA | 25853 |
rs565630423 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095015 | CTGTCAGAAAGCAAA[A/G]GTGTCCCATGTGAAA | 25853 |
rs565717523 | in-del | -/CC | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106041 | GTGTGAGCCACCACA[-/CC]CGGCCTATATTTTAA | 25853 |
rs565719339 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102857 | TAGGCAGGCAGGTCG[C/T]TTGAGGCCAGGACGT | 25853 |
rs565725721 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119603 | TTATCTTGTTAAAAA[C/T]GACTTTTCCTTTGGA | 25853 |
rs565867096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096274 | GTCTCAGCTACTTGG[A/G]AGGCTGAGGCAAGAG | 25853 |
rs565872645 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097716 | GGAGAGTGGATCAAC[G/T]GAGGTCAGGAGTTCA | 25853 |
rs565886931 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102521 | CAAAAATTAGTAGGG[C/T]GTGTGCCTGTAATCC | 25853 |
rs565948617 | in-del | -/T | 0.390838 | 0.206555 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100811 | GCCTTATTTTTTTAA[-/T]TTTTTTTTGTAGAGA | 25853 |
rs565951017 | snp | C/T | 1.6748e-05 | 0.00289374 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096813 | AACCAGGTTATATTA[C/T]CATCTATAGCAACTA | 25853 |
rs566002003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124112 | AACAGACACTTCTCC[C/T]AGTACTTAAGACTTT | 25853 |
rs566010029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098243 | TATGTAGCAAGCACT[C/G]ATGGGGAAGGAAAAA | 25853 |
rs566059764 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121707 | CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGCGGA | 25853 |
rs566084569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109760 | AAGCTCAGGCAGGTG[A/G]TGACCCCACTCACAG | 25853 |
rs566122374 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099691 | CACCACCTCCCGGGT[A/T]CAAGCGATTCTCCTG | 25853 |
rs566159811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090330 | CTCCCAAAGTGCTGG[G/T]ATTATAGGCATGAGC | 25853 |
rs566259921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093663 | AGATACTGAAGGAGA[C/T]AGGTTGGGGAAAAGG | 25853 |
rs566345360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094194 | CAGATCACCTGAGGT[C/T]AGGAGTTTGAGACCA | 25853 |
rs566376079 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128067 | CCGCAATGCTCTGGA[A/T]GACCCAAGAGCCCCT | 25853 |
rs566437548 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128769 | GTCTCAAAATCCTGA[A/C]CTCAGGTGATCCGCC | 25853 |
rs566502811 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087901 | ATCACACACACACAC[A/G]CAGACAAGATCTCTC | 25853 |
rs566876371 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092691 | CTCTGTCTCAAAAAA[A/C]AAAAACAACAACAAC | 25853 |
rs566968534 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120335 | CAGTGAGCCATGACT[A/G]CACCACTGTACTCCA | 25853 |
rs566997040 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089998 | TAATCTGCATATTTA[C/T]AAATCATTAAGTCAT | 25853 |
rs567010820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113427 | AGTGGCGTGATCTTG[A/G]CTCCCGGGTTCAAGT | 25853 |
rs567052119 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112708 | GTTCGAGACCAGCCT[C/G]ACCAACATGGAGAAA | 25853 |
rs567105430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119035 | AGTATAACAGCATTA[A/G]GACTTGAGGACCAGG | 25853 |
rs567111517 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123461 | CAAATAAGGGAATCA[-/T]TTGCCCAATGTCACA | 25853 |
rs567208028 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090248 | CTTGCATTTTCAGGA[C/G]AGACAGGGTTTCACC | 25853 |
rs567294520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090138 | GCGCGATCTTGGCTC[A/G]CTGCAACCTCTGCCT | 25853 |
rs567405960 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113884 | GAGGCCAAGGCAGGC[G/T]GATCATGAGGTTAGG | 25853 |
rs567424755 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086438 | AAGTCAAGTGCTACA[C/T]TTTTAAAAACAGAAA | 25853 |
rs567472700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093095 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 25853 |
rs567575058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112228 | TCTCTCTGAGATCCA[A/G]TAATACTTTCTGTTC | 25853 |
rs567608957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092204 | CACATAAAGTATACA[A/G]TTTGAGGTTCTGACA | 25853 |
rs567609710 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087236 | TTCCACACATGAAGC[A/T]CTCACTACACACAGA | 25853 |
rs567673337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097604 | TCTGACTCAATAAGG[C/T]AAGACTTAGTGGAAA | 25853 |
rs567703340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092643 | GTGAGCTGAGATCAC[A/G]CCACTACACTCCAGC | 25853 |
rs567823940 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113356 | TGTACGCGGCCTGAA[-/T]TTTTTCTTATTTTTT | 25853 |
rs568150700 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128567 | AGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT | 25853 |
rs568191946 | snp | A/G | 1.65699e-05 | 0.00287831 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089430 | CCAGCCTTTGCCAGT[A/G]GTTAGTTTCAGATTC | 25853 |
rs568294221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122053 | CAGCAGTTCTTCTTG[C/T]CCTGTAAATGTACAT | 25853 |
rs568358911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120442 | TTGGGAGGCTGAGGC[A/G]GGCAGATTACATGAG | 25853 |
rs568420352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114183 | AAATCCTTTGGACAA[C/T]ATGGATGAACCTAGA | 25853 |
rs568437233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113767 | TATTCACAATAGCCA[A/T]GATACGGAATCAGCC | 25853 |
rs568438788 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096235 | AAAAAAACAACCAGA[C/T]GGGTGTGGTGACACA | 25853 |
rs568476552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094360 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCATTCT | 25853 |
rs568535015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093863 | GCTGATCTCTGGCTA[C/T]CCCCAGCTCACCTTC | 25853 |
rs568597930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088710 | GAGAAGAACGGAGCA[C/G]CTGAAGAATTGCTAT | 25853 |
rs568650363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108566 | GGAGGCCAAGGCGGG[C/T]GGATCACCAGAGCTT | 25853 |
rs568707808 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093277 | TGAGGTGCACACAGG[G/T]ACTCTTACCACTGCC | 25853 |
rs568761408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100433 | TTGATCTCCTGACCT[C/T]GTGATCCACCTGCCT | 25853 |
rs568766139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115003 | CAAAAAAAAGAGGAA[A/G]GGGTAACCTTACAAT | 25853 |
rs568813533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101179 | TGGGCTTCAGCAATT[C/T]TCCTGCCCCAGCCTC | 25853 |
rs569055288 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101279 | AATGGGGTCTCACTA[C/T]GTTACCCAGGCTGGT | 25853 |
rs569064176 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120595 | AGAATCGCTTGAACC[C/T]GGAGGCAAAGGTTAC | 25853 |
rs569259582 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127055 | ACCAAACGTTTCCCT[A/G]AATCTGTCACAAACC | 25853 |
rs569264489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119125 | AGCTCCAAAAAACTC[A/G]CTGTGTGACTAAGAG | 25853 |
rs569323660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119730 | TTTTTGAGACAGGGT[C/T]GTGCTCTGTCACCCA | 25853 |
rs569325667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112854 | GGTAAGCTGAGATCA[C/T]GCCATTGCACTCCAA | 25853 |
rs569488073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113618 | GTGCTGGGATTACAA[A/G]CATGAGCCACCGCAC | 25853 |
rs569541962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116367 | ATAAATAAATAAATA[A/G]TACAAATAAATAAAT | 25853 |
rs569570140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099783 | ATTTTTAGTAGAGAC[A/G]GCGTTTCACCATGTT | 25853 |
rs569579062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123369 | ATATTGCTCACTCAG[A/C]ATATTTCCCAGATGC | 25853 |
rs569592531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115046 | CAAGGGTGTTTCAGA[C/T]TGGAGCCCAATGAGA | 25853 |
rs569608300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107680 | ACAACTACTACATGT[G/T]AGACCCTAGGAATTA | 25853 |
rs569626818 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123929 | TCTGGGTAAGACAAG[C/T]GACTCCTCAACAGAA | 25853 |
rs569690130 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF12 | GRCh38.p7 | 9:34116980 | CGAGACTCCGTCTCA[A/C]AAATCAATCATCAAT | 25853 |
rs569691496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109238 | GTGGTATCCTGTACT[C/T]GGACATGTTCATGCT | 25853 |
rs569728336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115362 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 25853 |
rs569732001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108678 | GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 25853 |
rs569753846 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098130 | TCAGAGAAATACTGC[A/T]GACACCAATTGAAGG | 25853 |
rs569816844 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095113 | GAGAGTCTTGCTCTG[C/T]TGCCAGGCTGGAGTG | 25853 |
rs569847017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111143 | GGCGTGCACCACCAC[A/G]CCCAGCTAATTTTTA | 25853 |
rs569989952 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100930 | AGGCATGAGCCACCA[C/T]ACCCAGACTAGGCCT | 25853 |
rs570011246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101403 | TTTATTTATTTATTT[A/T]GGTGGTGGGACAGAG | 25853 |
rs570177123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095469 | CACTGCAGCCTTGAC[C/T]TCCTCAGCTCAAGTG | 25853 |
rs570192950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096061 | GAGAACTGGTCTTTT[A/C]AACAAGAATTGAGAC | 25853 |
rs570223391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089682 | ACACTGAGTTTTCAA[C/T]GTCCACCCTGCTCCC | 25853 |
rs570410121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34090204 | AAGTAGCTGGGATTA[C/T]AGGCTCCTGCCATCA | 25853 |
rs570452805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122349 | ATGACTGCCAAATCA[C/T]TAACTTCAATCCTTA | 25853 |
rs570469225 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109394 | GTTGTTGCCAATGAC[A/G]GTGGCAGCCATCTTT | 25853 |
rs570512947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114786 | ACAAATGTAAATGAG[C/T]GTACACAAAGACAAA | 25853 |
rs570514105 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115590 | GCGACAGAGCAAGAC[G/T]TCGTCTCAAAAAAAA | 25853 |
rs570824429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108106 | CATTCAGTCCTATTC[A/C]TCCCTGCCTTTGCTC | 25853 |
rs570858705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114291 | ATCTTGGCTGGATGC[A/G]GTGGCTCACACCTGT | 25853 |
rs570924739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111378 | AATGTCCAGGCTGAT[C/G]AAGTGCCTCTCTTGT | 25853 |
rs570989571 | snp | C/T | 1.68383e-05 | 0.00290153 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125318 | GGCTTTGGCTACTCT[C/T]CTTCAGAACAGATCC | 25853 |
rs571010318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102009 | GACAGAGTGAGACCC[C/T]GTCGCAAAAAAAAAA | 25853 |
rs571078888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101332 | CCTGCTTCAGTCTCT[C/T]GAAATACTGGGACTA | 25853 |
rs571151254 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088883 | AGGAGGCCAAGGTGA[A/G]AGAATCACTTGAGCC | 25853 |
rs571189791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095364 | AGGCGTGAACCACCG[C/T]GCCAGGCCTTTTTTT | 25853 |
rs571296442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096867 | GATTCTAAGGTCAGG[G/T]TCCTTTATTCCTGTC | 25853 |
rs571306852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096337 | TGATCCATGAGCCAT[A/G]ACTGCACTCCAACTT | 25853 |
rs571342306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099008 | CTCCTGAGTTCCAGC[A/G]ATCAGCCTGCCTTGG | 25853 |
rs571357229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105114 | AAAAATTAGCCTGGC[A/G]TGGTGGTGGGCACCT | 25853 |
rs571369351 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112020 | TGGTGGCGGGCGCCT[G/T]TAATCCCAGCTACTC | 25853 |
rs571443789 | snp | C/T | 0.000280068 | 0.0118303 | missense | DCAF12 | GRCh38.p7 | 9:34098445 | GGGACCCGTGACACA[C/T]TGTGTCTCGCATCAC | 25853 |
rs571512817 | in-del | -/GATAGA | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091616 | TCCTCCAGCCTGGCT[-/GATAGA]GATAGAGTGAGGACC | 25853 |
rs571524159 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119544 | TTATCACTATTTACT[G/T]AAGTATTCGATTGTT | 25853 |
rs571563628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092876 | TTGAGACAGAATTTC[A/G]CGCTCATTGCCCAGG | 25853 |
rs571638511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103669 | CAGCAGCCTGGGCAA[C/T]AAAGCGAGACCCAGT | 25853 |
rs571801308 | snp | C/T | 1.65222e-05 | 0.00287417 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125019 | CATCCCCCCAGGCAC[C/T]TACCGTGTTGCATTT | 25853 |
rs572042116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109918 | ACGGAGAGGGTGACA[C/T]TGTAGGGCTCTACCA | 25853 |
rs572067548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103265 | AAGACAAACCAGCCC[A/G]GCGTGGTGGCACGCG | 25853 |
rs572130834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103820 | CACTCCAGCCTACAT[A/G]ACAGAGTGAGACCCT | 25853 |
rs572136859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096496 | ATCCCCGCAGCTACT[C/T]AGGTGGCTGAGGCAC | 25853 |
rs572148447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091074 | CTCAAGCCTGTAATC[C/T]CAGTACTTTGGGAGG | 25853 |
rs572196940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091628 | GGCTGATAGAGTGAG[A/G]ACCCTGTCTTCAAAA | 25853 |
rs572268055 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098607 | CTTTCATAGTCTAGC[G/T]GTTTGTGCATCATCC | 25853 |
rs572274310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097053 | TGTTGGAGAGTTAAA[A/G]CAGGGCACATATGTG | 25853 |
rs572340021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089220 | ACCAGTGTGTTTTAC[G/T]GGGCCTCAGTTTTCC | 25853 |
rs572353059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122763 | GATTACAGGTGTGAG[A/C]CACCTTGCCCTGCGA | 25853 |
rs572354894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124455 | GTCTTTCTATTCACT[C/T]TTAAAAAGGCTACTT | 25853 |
rs572382739 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119197 | AGCCCCTACTTCGGT[C/G]CTTCTCACCGTCATT | 25853 |
rs572418424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34123580 | CAGCTCCCCTTGCCC[C/T]AAACACTAGGTTATG | 25853 |
rs572433190 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098780 | TTTATTATTATTATT[A/T]TTTTTTGAGACAGAG | 25853 |
rs572438877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106775 | ATCTGGAACTCTCTT[A/C]CTCCAGACATCTAGA | 25853 |
rs572494652 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105888 | TGAGCAGCTGGGACT[A/G]CAAGCGCCCACGACC | 25853 |
rs572506826 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104879 | GCCAAGATTGCACCA[C/T]TGCACTTTAGCCTGG | 25853 |
rs572534342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089772 | AAAGCAAAGAGAATC[C/G]TGATGCCATCCTGCC | 25853 |
rs572605823 | snp | A/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126599 | ATAGGCGGAAAGAAA[A/G]GAAAGAGAGAGGAAG | 25853 |
rs572624272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34109585 | AGAGGGGGGTCCCAC[A/G]CAGCCATCATATTCT | 25853 |
rs572834530 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090034 | ATTCCTTATATTTCA[C/G]CTAAAACCACTACTG | 25853 |
rs572878381 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086542 | TTTTTTTTTAAATAT[A/G]CAAGTCAGTTTAAAA | 25853 |
rs573076993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098071 | AGTCAAATCAGGGTG[A/G]CCCTAGGGGAATTCT | 25853 |
rs573165646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098726 | AAGGTCTAGGCATTA[A/C]AATATAACTTTTAAG | 25853 |
rs573204940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117298 | AAAAAAAAAAGGTGC[C/T]CACCACCACGCCCGG | 25853 |
rs573317428 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118239 | CCCGGGTTCAAGCGA[A/C]TGTCCTGACTCAGAC | 25853 |
rs573322700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125430 | AATCTCAATCCAGAA[A/G]GTCGTTTAACTCTTC | 25853 |
rs573347012 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088720 | GAGCAGCTGAAGAAT[G/T]GCTATACAAGGCTCA | 25853 |
rs573355285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105276 | AAAAAAATCATACTA[A/T]GGCTGGGTGCAGTGG | 25853 |
rs573384921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117902 | CTGGGCAACAAGAGC[A/G]AAACTCTGTCTCAAA | 25853 |
rs573420253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104763 | TCTACTAAAAAATAC[A/G]AAAATTAGCCAGGCG | 25853 |
rs573545210 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126532 | GGGGCCGCGCACCTT[A/G]GTGCGCCCGGCCCGG | 25853 |
rs573852283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112448 | AAAATACAAAAATCA[C/G]CCAGGTGTGGTGGCG | 25853 |
rs573885281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118710 | GGGTCATGCATATAA[A/T]CCCAGCTCTTTGGGA | 25853 |
rs573928884 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110992 | TCTTTTCTGTTTTTT[G/T]TTTTTTTTTTTGAGA | 25853 |
rs573951155 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34104518 | TCTCTCAAAGATTTG[A/C]GCATCAGAGTGAGAA | 25853 |
rs574088836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124374 | TTTGACTTATTTTAT[C/T]CTGGCCTATAATTGG | 25853 |
rs574114455 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099072 | CCACACCTGGTCTGC[-/T]TTTTTTTTTTTTTGA | 25853 |
rs574218993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097331 | CTGTGGCGCAATTTC[A/G]GCTCACTGCCAACCT | 25853 |
rs574289693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34100836 | TAGAGATGGAGTCTC[A/G]ATTTGTTGCCAAGGC | 25853 |
rs574289734 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108798 | GACTTGGTCTCAAAA[A/T]AAATAAATAAATAAA | 25853 |
rs574303210 | in-del | -/TTG | 0.00239521 | 0.0345234 | intron-variant | DCAF12 | GRCh38.p7 | 9:34091850 | TAAAGAAAATACAAT[-/TTG]TTAAGTTGGATTCTG | 25853 |
rs574350507 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101518 | CTACCTCAGCCTTCC[A/G]AGTAGCTGGGATTAC | 25853 |
rs574455354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120623 | TACAGTGAGCCAAGA[C/T]CGTGCCACTGCACTC | 25853 |
rs574485044 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120241 | AAAAAAAAGGCCAGG[G/T]ATGATGGCATGTGAT | 25853 |
rs574637997 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127177 | GGGCAGTGTGGCCAG[A/G]CTTTCCCACCACTGA | 25853 |
rs574644615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103675 | CCTGGGCAACAAAGC[A/G]AGACCCAGTCTCTAT | 25853 |
rs574708308 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101888 | AGGCGTGGTGGGGCA[C/T]GCCTGTGGTCCCAGC | 25853 |
rs574771402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34112871 | CCATTGCACTCCAAC[A/C]TGGGCAATAAGAGCG | 25853 |
rs574881477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106059 | GGCCTATATTTTAAA[A/T]TTTTCTTACAATAAA | 25853 |
rs574917519 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086641 | AATTAAAAGATCTAT[A/C]GCATCCAGCATTTTG | 25853 |
rs574920287 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105481 | TTATATTTTAAAATG[C/T]CAACAGTCGTTATTA | 25853 |
rs574927103 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093944 | TTAATCCCAGATAAC[A/C]CACATCAGCCTTAAC | 25853 |
rs574982842 | snp | C/T | 6.59772e-05 | 0.00574319 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093250 | AACCCATATGCAGTG[C/T]AGCTGTAGGCCTGAG | 25853 |
rs575092921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099829 | GAACTCCTGACCTCA[C/T]GATCCACCCGCCTCA | 25853 |
rs575124759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34113922 | GACCATCCTGGCTAA[A/C]ACAGTGAAACCCCGT | 25853 |
rs575132053 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093985 | CGTCAGTTAGCAAAT[C/G]CTCAGTGGGTGCATA | 25853 |
rs575166725 | in-del | -/T | 0.36606 | 0.221428 | intron-variant | DCAF12 | GRCh38.p7 | 9:34117256 | ATTTCTAATCCTTGA[-/T]TTTTTTTTTTTTTTG | 25853 |
rs575168188 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128266 | TTTTCTTTTTTTTTT[C/T]TTGAGATGGAGTCTC | 25853 |
rs575217799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34120060 | ACAAAAAAATTAGCC[A/G]GGCTTGGTGGTGGGC | 25853 |
rs575247588 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128229 | ATCCCCAAATGTACC[C/T]TATAGCAGAGCTCGC | 25853 |
rs575300786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34119444 | CAGAGACAGGATTTT[A/G]TATCTCATTTCATTA | 25853 |
rs575483566 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104218 | TGCAGTGAGCCAAGA[C/T]GCACTCCAGCCTGGG | 25853 |
rs575566569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093198 | CCATACAGAGCACTA[C/T]ACCTGTTTGGAAACC | 25853 |
rs575646628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34105339 | GCTGAGGCAGGAGGA[C/T]AGCTTGAGCCCAGGA | 25853 |
rs575738369 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF12 | GRCh38.p7 | 9:34111697 | CAGTCTAGAGGGAGT[C/T]TCAGGACAATCAGTC | 25853 |
rs575739711 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109435 | GTGGGATGTTACAGA[C/T]AGCTGTTTTCACCTT | 25853 |
rs576009545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102504 | TGTCTCTACTAAAAA[G/T]ACAAAAATTAGTAGG | 25853 |
rs576136325 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108942 | CAAAACAGCAAGACC[C/T]TATCTCAAACAAATA | 25853 |
rs576165230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095828 | AAGGTTCCTAACACT[C/T]AGGATTTCCTTCCCT | 25853 |
rs576181975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096455 | AATACAAAAAAAATA[A/C]CTGGGCATGTTGGCA | 25853 |
rs576182245 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118129 | ATTGATTTATTTCTT[C/T]TGTTTTTTTTCCAAG | 25853 |
rs576321929 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103080 | ATCCTGGGTGACAGG[A/G]CGAGACCTTAACTCC | 25853 |
rs576419926 | in-del | -/AG | 0.00478085 | 0.0486577 | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086057 | TATGCAAGCACTTTC[-/AG]CGTCATTCTCAGGGC | 25853 |
rs576492655 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119688 | TCTTTCAACAAATAC[C/T]ATGTACTTTTGCGGT | 25853 |
rs576628490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095177 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 25853 |
rs576643046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122426 | TCTGTTCCTTAACAT[G/T]CACCCTGCCATCTTT | 25853 |
rs576708537 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094132 | AGAAAAAGCTGGGCG[C/T]GGTGGCTAACGTCTG | 25853 |
rs576763783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34095762 | TTCTCATTACCTTAC[A/G]TGATTATTTCAGAGA | 25853 |
rs576776575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115099 | TCACACAGACAACAA[A/G]ACACACTATGTTGCA | 25853 |
rs576813402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34108824 | ATAAATATATATATA[C/T]ATATATGAATGAGGT | 25853 |
rs576897609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34115075 | GAAAGGAAAGTAATT[A/C]TACGCAGGTCACACA | 25853 |
rs576942785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34114509 | CACCCTGCTTCTTCA[C/T]GGGAAGAAACAGGAT | 25853 |
rs576977722 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34101627 | GAACTCCTGACCTCA[C/G]GTGATCCACCCTCCT | 25853 |
rs577205916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106994 | ATGTTTTGTCTATAT[G/T]TCACCCTCCACTAGA | 25853 |
rs577323595 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104918 | CAAGACTCCGTCTCC[-/A]AAAAAAAAAAAAGAA | 25853 |
rs577355108 | snp | A/T | 1.64749e-05 | 0.00287005 | splice-acceptor-variant | DCAF12 | GRCh38.p7 | 9:34088510 | GTTTCATCATGATTC[A/T]ACGGGAAGAGAAAGA | 25853 |
rs577370838 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087534 | GTCTGATGTTTTAGG[A/G]GTGTGGCTACTGGCT | 25853 |
rs577514390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF12 | GRCh38.p7 | 9:34094653 | CTCCTGCCTCAGCTT[C/T]CCGGGTAGCTGGGAC | 25853 |
rs577538630 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34099339 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCCCA | 25853 |
rs577696229 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111459 | ATTTAAAATATTTAC[C/T]TATTTGTCTTCCTCA | 25853 |
rs577711415 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF12 | GRCh38.p7 | 9:34097228 | TGGAGAAGCCTTTCT[C/G]TGGCTCTGGGTGTAT | 25853 |
rs577716908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34122856 | ATGCCTTCTGTAGTT[C/T]TTTGCAGCCCCTACT | 25853 |
rs577739145 | in-del | -/A | 0.392881 | 0.205147 | intron-variant | DCAF12 | GRCh38.p7 | 9:34102283 | TAAGACCCTGCCTCC[-/A]AAAAAAAAAAAGAAT | 25853 |
rs577829443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126233 | ATAGGCCCTGAACCC[A/G]TTCCTGTTTTGCCTC | 25853 |
rs577868986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110753 | GGTGCCACTGCACTC[A/G]CACCTGGGTGACAGA | 25853 |
rs577937256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34092292 | CTGAGGTTTCCTCAT[A/G]CCCTTTGTAAACTTC | 25853 |
rs577975555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34118075 | CAATAGTCTGATTTC[A/G]TAAGAATCTTTATTT | 25853 |
rs577987776 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110461 | CTTTGTGCCTTCAGG[C/G]AACACCGCTATCAAA | 25853 |
rs578016315 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34125000 | CGACCTAGGAGAGAG[A/G]TCACATCCCCCCAGG | 25853 |
rs578103513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34110001 | TTAAATTATATATAA[C/T]TATATATGTATATAT | 25853 |
rs578122321 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095986 | AAAAGACTTTCCTGC[A/G]AGAGAGGCACACCAG | 25853 |
rs578148151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF12 | GRCh38.p7 | 9:34103445 | AAAAGTAAGTTTATA[A/T]TCCCATTCAGAAACA | 25853 |
rs578219602 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093272 | AGGCCTGAGGTGCAC[A/G]CAGGGACTCTTACCA | 25853 |
rs745315988 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112073 | GCTTAAACTCAGGAG[A/G]TGGAGGTTGCAGTGA | 25853 |
rs745321497 | snp | C/T | 0.0002735 | 0.0116908 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098296 | AGCAAGAGGAATACA[C/T]GTCAGGGATCCCTAC | 25853 |
rs745401486 | snp | C/G | 1.79178e-05 | 0.00299309 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088339 | AAATCTCTGCATTTG[C/G]GGAGTTGTCATTAAC | 25853 |
rs745401504 | snp | C/T | 2.16894e-05 | 0.00329306 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34106438 | GGCAACTTTACCAGA[C/T]ACTGCCATAGTGTCG | 25853 |
rs745535561 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124083 | TGTTTAAATTTTTGC[C/T]TATGTCCTTTATAAA | 25853 |
rs745562484 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | DCAF12 | GRCh38.p7 | 9:34088462 | TAAACAGCATTGGGG[A/G]AGAAGTCAATGTCTG | 25853 |
rs745579450 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127602 | TGGCCTCCAAACAAG[A/G]GGGCTTCATCAGGAT | 25853 |
rs745616853 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118624 | GCAGAGACGGTAATT[A/G]CGTATCTGGTATAAG | 25853 |
rs745617855 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125164 | ACCATGCAACACTCG[A/G]GAGTAGCTGGTTTCA | 25853 |
rs745623290 | snp | G/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086723 | CCAGAACCTGTGGTA[G/T]GTGCTGTGTAACAAG | 25853 |
rs745777273 | snp | A/C | 1.65146e-05 | 0.0028735 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125262 | TCCTTTTGTGAAGCG[A/C]GTGATCCCAGCCAAA | 25853 |
rs745822844 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117537 | TGATTTTACCTAGTA[C/G]CCACCAAAGTCACCA | 25853 |
rs745995110 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100496 | AGACACCACGCCCAG[A/C]TTCTTTTTTTTTTTT | 25853 |
rs745996694 | snp | A/G | 0.00145773 | 0.0269581 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127217 | CAGCACAACCAACCC[A/G]GGCCGCCCTACGAGT | 25853 |
rs746005104 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102535 | GCGTGTGCCTGTAAT[-/C]CCAGATACTTAGGAG | 25853 |
rs746018479 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119655 | TTTAGGCAAAAGGGT[A/G]TAACATTTTTAGGCT | 25853 |
rs746059600 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107994 | TCATGGCTACTAATA[A/T]AACTATTAATATTAC | 25853 |
rs746126986 | in-del | -/TTTTTTTTT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095374 | CACCGCGCCAGGCCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 25853 |
rs746156000 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103575 | AATTATGTTTTAGGC[C/T]GGGCATAGTGGCTCA | 25853 |
rs746171298 | snp | A/C | 1.64817e-05 | 0.00287064 | missense | DCAF12 | GRCh38.p7 | 9:34089470 | AGTCTGGGCTTGGAC[A/C]CATAACAAGCTGAGA | 25853 |
rs746261139 | snp | A/C/G | 3.30651e-05 | 0.00406591 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089553 | CTGCCCTGTTCCCAC[A/C/G]GTGATGATGTGCTCG | 25853 |
rs746280318 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089006 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGGA | 25853 |
rs746292905 | in-del | -/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128417 | ACGTTGCCCAGCTAA[-/T]TTTTTTTTTTTCTTT | 25853 |
rs746294028 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104228 | CAAGATGCACTCCAG[C/G]CTGGGCGACAGAGCG | 25853 |
rs746377084 | snp | A/C | 1.84228e-05 | 0.00303497 | synonymous-codon, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126357 | CTCAACCCTCACCTG[A/C]GGGCCCTGAGCGTCG | 25853 |
rs746394194 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114825 | AAAAAAAAGGAGTCA[A/G]ATGTGGTAGCAGGAA | 25853 |
rs746445860 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122924 | CTTAGCTTTTCTGTC[C/T]GGCTCCGCAGCCAAT | 25853 |
rs746464917 | snp | A/C | 2.12456e-05 | 0.0032592 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126438 | CCGGGCCATAGTGGG[A/C]AGCGCCGCCGCGGCC | 25853 |
rs746566240 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111144 | GCGTGCACCACCACG[C/T]CCAGCTAATTTTTAT | 25853 |
rs746624424 | snp | A/G | 9.88419e-05 | 0.00702931 | missense | DCAF12 | GRCh38.p7 | 9:34098391 | GTGTCTTCTTTGGGG[A/G]TGTCCTTTAAGGCCT | 25853 |
rs746645150 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090372 | GCCACAATGCAAGAA[A/G]TCTTTATCTAGTATT | 25853 |
rs746713890 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | DCAF12 | GRCh38.p7 | 9:34098468 | CGCATCACTTTTGGT[A/C]AAAACATCATCTGTC | 25853 |
rs746749317 | snp | C/T | 1.79774e-05 | 0.00299806 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088331 | GTTAGTGTAAATCTC[C/T]GCATTTGGGGAGTTG | 25853 |
rs746910814 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092923 | CGATCTCAGCTCACC[A/G]CAACCTCCGCCTCCC | 25853 |
rs746927847 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098135 | GAAATACTGCAGACA[C/T]CAATTGAAGGGGTGG | 25853 |
rs746939650 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125047 | TTTTGTGCCACACAC[C/T]ACTTGCCTATGATTC | 25853 |
rs747013424 | snp | C/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127178 | GGCAGTGTGGCCAGA[C/G]TTTCCCACCACTGAG | 25853 |
rs747020535 | snp | C/T | 8.26003e-05 | 0.00642599 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106452 | ACACTGCCATAGTGT[C/T]GCTGATCCATGCGAT | 25853 |
rs747140283 | snp | A/G | 1.70156e-05 | 0.00291677 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096678 | TTTAACTGTAAGGTG[A/G]ATTATTAGGTAAAAC | 25853 |
rs747171106 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093719 | TAGCTGGAAAGGCCA[A/C]GGCCTTTCTTGGTAG | 25853 |
rs747327833 | snp | A/G | 1.99894e-05 | 0.00316138 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106465 | GTCGCTGATCCATGC[A/G]ATGGAAAAGATCCAG | 25853 |
rs747377395 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119760 | AGGCTAGAGTGCAGT[A/G]GTGTAATCCCATTTA | 25853 |
rs747400356 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101794 | CTGAGGTAGGTGGAC[C/T]GCCTGAGCTCAAGAG | 25853 |
rs747447158 | snp | A/G | 0.000115324 | 0.00759268 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088513 | TCATCATGATTCTAC[A/G]GGAAGAGAAAGAGAC | 25853 |
rs747472881 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114556 | AGAATCTCTTCCCAA[G/T]CTCTCTGACAAGGGT | 25853 |
rs747538770 | snp | A/G | 0.000124046 | 0.0078745 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125669 | CTCCCACTGGAGCAC[A/G]GAAGATACAGTCCAA | 25853 |
rs747575064 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112422 | CCAACATGACGAAAC[C/T]ATCTCTACTAAAAAT | 25853 |
rs747611926 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089451 | TTTCAGATTCTCCCC[C/T]GCTAGTCTGGGCTTG | 25853 |
rs747655364 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086959 | CTTAGAGGAACTGGT[A/G]GGTGGGAACAGCTGT | 25853 |
rs747679094 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121741 | CGAGGTCAGAAGATC[A/G]AGACCATCCTGGCCA | 25853 |
rs747732957 | snp | C/T | 1.85837e-05 | 0.0030482 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126347 | GTGCCGGCCTCTCAA[C/T]CCTCACCTGCGGGCC | 25853 |
rs747824831 | snp | A/C/T | 5.15047e-05 | 0.00507446 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098279 | GCATATCCCAAGACA[A/C/T]AAGCAAGAGGAATAC | 25853 |
rs747896183 | snp | C/T | 0.000402138 | 0.0141742 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096704 | AAAACCACAAAATCA[C/T]GTTCATCACACCTTA | 25853 |
rs747897847 | snp | C/G | 2.02218e-05 | 0.0031797 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126425 | TGCTAACTACTTTCC[C/G]GGCCATAGTGGGCAG | 25853 |
rs747964614 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097633 | AATGTGAAGGGAAAG[C/T]AGGCAGTAAAGAATA | 25853 |
rs747996526 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097831 | CCAGCTACTTGAGAA[C/T]CTGAGGCAGAAGAAT | 25853 |
rs748100145 | snp | C/T | 1.6625e-05 | 0.00288309 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107556 | TTGTCTGGACATCTA[C/T]GACAAATAGCTACAA | 25853 |
rs748107858 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104658 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCATTTT | 25853 |
rs748189668 | snp | A/G | 1.65048e-05 | 0.00287265 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125024 | CCCCAGGCACTTACC[A/G]TGTTGCATTTTGTGC | 25853 |
rs748284956 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090778 | TCCTGCCTCAGCCTC[A/C]CAAGTAGCTGGAACT | 25853 |
rs748316920 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105489 | TAAAATGTCAACAGT[C/T]GTTATTACTAGCTGG | 25853 |
rs748404737 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116261 | ACTCGGGAGGCTGAG[A/G]TAGGAGAATCGCTTG | 25853 |
rs748407896 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124285 | CACCCCTAGGCCCTA[A/G]GCCCTGCCTCTTTTC | 25853 |
rs748441165 | snp | G/T | 0.000461141 | 0.0151775 | missense | DCAF12 | GRCh38.p7 | 9:34093389 | TGCATAAACTGACCA[G/T]TCACTACCATAAGCC | 25853 |
rs748549663 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102852 | AGGCTTAGGCAGGCA[C/G]GTCGCTTGAGGCCAG | 25853 |
rs748571739 | snp | A/G | 1.71021e-05 | 0.00292416 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098532 | CCTGCAGGGCCAGGA[A/G]AACACAGATGTCAGA | 25853 |
rs748615856 | in-del | -/ATC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118582 | TTAACAGGGAGCTTT[-/ATC]ATCCCTAACTTGCAA | 25853 |
rs748656276 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092351 | CATAAATAGAATTTT[A/G]GTTCAGGCAGGACCA | 25853 |
rs748688905 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108843 | TATGAATGAGGTGGA[C/G]AAGGTGGCAAGTGCC | 25853 |
rs748723785 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123601 | CTAGGTTATGAGGAT[C/T]AGGAAGACAGAAAGA | 25853 |
rs748761501 | snp | A/C | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087034 | ACAGTCAGCTGCCTG[A/C]AAGTTTAAAAACCTC | 25853 |
rs748775237 | snp | C/T | 8.2373e-05 | 0.00641714 | missense | DCAF12 | GRCh38.p7 | 9:34088486 | ATGTCTGAAAAGTAA[C/T]TCCTCCAGGTTTCAT | 25853 |
rs748780217 | snp | A/G | 1.66624e-05 | 0.00288633 | missense | DCAF12 | GRCh38.p7 | 9:34089417 | GCTTACGCACCAGCC[A/G]GCCTTTGCCAGTGGT | 25853 |
rs748784066 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126831 | AGTTCTCTGGTGTTT[C/T]CCGGCCGCCGCCAGG | 25853 |
rs748840717 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118678 | TGTTAAATAATGATA[A/G]TATGGCCGGGCGTGG | 25853 |
rs748903747 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089645 | AATATTTGCTGACTG[C/T]CTGCTAGCCTGAATT | 25853 |
rs748923794 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099737 | CAGTTGGGACTACAG[A/G]CACACGTCACCATGC | 25853 |
rs748961840 | snp | A/T | 1.66821e-05 | 0.00288804 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125297 | GGAAACAACATTAGA[A/T]ATCAGGGCTTTGGCT | 25853 |
rs749024892 | snp | C/T | 1.66624e-05 | 0.00288633 | splice-donor-variant | DCAF12 | GRCh38.p7 | 9:34096715 | ATCATGTTCATCACA[C/T]CTTAGATAGTGTATT | 25853 |
rs749042634 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108327 | AACACAGCTATGAAC[A/G]AGAGAAATAATATCT | 25853 |
rs749080082 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102282 | GTAAGACCCTGCCTC[-/A]CAAAAAAAAAAAGAA | 25853 |
rs749093600 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109697 | CAGACATGAAGAAGT[A/G]CAAGCGGGGGAATAG | 25853 |
rs749193353 | snp | C/T | 1.69146e-05 | 0.0029081 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096827 | ATCATCTATAGCAAC[C/T]AATGTACGATAATAA | 25853 |
rs749248664 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119578 | ATTTAGATTAAGTAG[C/T]TTCCAATTATTATCT | 25853 |
rs749266587 | in-del | -/G | 2.66301e-05 | 0.00364888 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126482 | GGCGGGGGAAGCGAA[-/G]GGATAGCAGGACGGC | 25853 |
rs749404281 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095456 | CAAAATTACGGCTCA[C/T]TGCAGCCTTGACCTC | 25853 |
rs749440367 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103630 | AGGCTCAAGTGGGAG[G/T]ATCGCTTGAGCCTAG | 25853 |
rs749500566 | snp | G/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127583 | GTCCAGTTAGAGCTG[G/T]CATTGGCCTCCAAAC | 25853 |
rs749531239 | snp | A/G | 1.66821e-05 | 0.00288804 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124997 | CCACGACCTAGGAGA[A/G]AGGTCACATCCCCCC | 25853 |
rs749551036 | in-del | -/AAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090562 | GATAATATTTGTGGA[-/AAT]ACCAGTATTTCCTTA | 25853 |
rs749553077 | in-del | -/C | 5.06393e-05 | 0.00503161 | frameshift-variant | DCAF12 | GRCh38.p7 | 9:34088397 | CCCTGAAGGGAGGGG[-/C]ACCTCCTGCCACAAA | 25853 |
rs749573267 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115760 | TCTTTTTTAATTATA[C/G]AGACAGGGTGCCACT | 25853 |
rs749579942 | snp | A/G | 8.30489e-05 | 0.00644341 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089568 | AGTGATGATGTGCTC[A/G]TAGAAACTCACTGAC | 25853 |
rs749611337 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090563 | GATAATATTTGTGGA[A/G]CCAGTATTTCCTTAT | 25853 |
rs749661302 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091877 | ATTCTGGTCCCTAGC[A/T]GTTCCCCCATCAAGC | 25853 |
rs749708440 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123085 | GATAAAAACAACAGT[A/G]GCTATCCTTGCTGTT | 25853 |
rs749751258 | in-del | -/ACATC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103045 | CAGTGAGCCATGATC[-/ACATC]ACGCCACTGCATTCC | 25853 |
rs749769212 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104456 | TAGGTGTGGGCCTTG[C/T]ATGCTGTGCTATAAA | 25853 |
rs749874289 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | DCAF12 | GRCh38.p7 | 9:34098414 | TAAGGCCTTGTGAGT[C/G]ATGTGTGCATACACA | 25853 |
rs749874585 | snp | A/C | 9.6214e-05 | 0.00693525 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127246 | GTCTCTGGCTACCCT[A/C]TTCCCACCGCTGGGT | 25853 |
rs750015423 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126637 | GCCGGGAAAGGGAAG[A/G]GGAAGCGAGAATGAG | 25853 |
rs750061408 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112322 | GATCCCAGGCTGAGC[A/G]TGGTGGTTCACGCCT | 25853 |
rs750084239 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096293 | CTGAGGCAAGAGGAT[-/C]GCTTATGCCCAGGAG | 25853 |
rs750123053 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094450 | ACAGGTAGGTTTAAC[C/T]CTATGTAAAAGTTGC | 25853 |
rs750149911 | snp | A/G | 2.59649e-05 | 0.00360302 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106545 | AATAAGAAATTAGTA[A/G]AATAAGGATTGTAAT | 25853 |
rs750185860 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088657 | TGGCTGGTTGGTTCT[C/T]ATGGGAATCAGGGCC | 25853 |
rs750237929 | snp | G/T | 1.71455e-05 | 0.00292787 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089396 | TAGCAGTCATCTCAG[G/T]TAGGGGCTTACGCAC | 25853 |
rs750255279 | in-del | -/TTTT | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128256 | TCGCGATTTCTTTTC[-/TTTT]TTTTTTTTTGAGATG | 25853 |
rs750266445 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089511 | CAGAAATCTCTGAGC[C/T]CGGATGTCATAGAAC | 25853 |
rs750338849 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101140 | GCAATAACATGATTA[C/T]GGCTCATTGTAGCCT | 25853 |
rs750356779 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114140 | CACAGATACACAATG[C/T]AATACTGTTTAGCTA | 25853 |
rs750395514 | snp | A/G | 0.000231623 | 0.0107591 | missense | DCAF12 | GRCh38.p7 | 9:34088420 | GCCACAAAGAGTTTC[A/G]TTCCAGACGAGTCGT | 25853 |
rs750421260 | snp | C/G | 0.000122617 | 0.007829 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125649 | CTTCTCCCTCTCAGT[C/G]TGTACTCCCACTGGA | 25853 |
rs750449107 | snp | A/G | 1.67156e-05 | 0.00289093 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096803 | GAGCAATGAAAACCA[A/G]GTTATATTATCATCT | 25853 |
rs750479632 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110397 | CTTACAGCTGACTCC[C/T]TCCTCTGCTTCCTCA | 25853 |
rs750540732 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096250 | TGGGTGTGGTGACAC[A/G]TGCCCATAGTCTCAG | 25853 |
rs750640068 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121602 | GATCATCACTCTGCC[A/G]ATTGCCATCCTTCTC | 25853 |
rs750676312 | in-del | -/TAAGA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117090 | ACACTACTAGCTAGC[-/TAAGA]TAAGTAATGGTACTT | 25853 |
rs750716816 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116101 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 25853 |
rs750745505 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115664 | TCTCCCCATAGACAT[-/AT]ATATATATAGCTTGT | 25853 |
rs750748673 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110047 | TATTTAAATATATAT[-/A]ATATATGTTTATTAA | 25853 |
rs750957096 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097128 | ACTCTAATTTAGGAG[A/C]GATTAATCTACCCTT | 25853 |
rs750975946 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093243 | AAGTCAGAACCCATA[C/T]GCAGTGCAGCTGTAG | 25853 |
rs751062810 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | DCAF12 | GRCh38.p7 | 9:34093337 | TGTATGATGGCTGCC[A/G]TGGATCCAAGAAGGA | 25853 |
rs751083476 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092877 | TGAGACAGAATTTCG[C/T]GCTCATTGCCCAGGC | 25853 |
rs751129239 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099895 | GTGCACCTGGCCAAA[C/G]CTTAGTAATTTTCTA | 25853 |
rs751151511 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104917 | GCAAGACTCCGTCTC[-/A]CAAAAAAAAAAAAGA | 25853 |
rs751178554 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123868 | GAGAGACCAAGAAAA[C/G]GAAGTTCTGTGGAGG | 25853 |
rs751318242 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098916 | TGGGATTACAGGTGC[C/G]TGCTCCATGCCTGGC | 25853 |
rs751329327 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100956 | GGCCTCTTTTTCTAG[A/C]AAATTACACAAAACA | 25853 |
rs751355954 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120946 | ATCACCTGAGGTCAG[G/T]AGTTCGAGACCAGCC | 25853 |
rs751420114 | snp | A/G | 4.35066e-05 | 0.00466384 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106522 | GGAGTAACAGGTACA[A/G]GGAGGAAAATAAGAA | 25853 |
rs751518054 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124981 | AAGTGGAGCAATATA[G/T]CCACGACCTAGGAGA | 25853 |
rs751533345 | in-del | -/G | 0.000350822 | 0.0132396 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125302 | CAACATTAGAAATCA[-/G]GGCTTTGGCTACTCT | 25853 |
rs751555763 | snp | A/G | 3.47029e-05 | 0.00416537 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089383 | TTCTGTTACTGTGTA[A/G]CAGTCATCTCAGGTA | 25853 |
rs751603543 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125253 | GAAGTCTTTTCCTTT[C/T]GTGAAGCGAGTGATC | 25853 |
rs751626305 | snp | C/T | 0.000121632 | 0.00779752 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125581 | AAAGATTGAAGGAAA[C/T]GAGAGGTAGAGTGAT | 25853 |
rs751745260 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121185 | AACAAAAAAACCCAA[A/G]AACACTGACTAAACC | 25853 |
rs751775579 | snp | A/G | 1.66729e-05 | 0.00288724 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096793 | GTTCCTACAAGAGCA[A/G]TGAAAACCAGGTTAT | 25853 |
rs751862268 | snp | C/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127028 | CCTTAACCCGGTTAC[C/T]TCCCATCTGGCACCA | 25853 |
rs751907780 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096093 | AGGTGCAATGGTTCA[C/T]GCCTGAATGCCCAGC | 25853 |
rs751911389 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088625 | GGTTCTACAGGTACA[A/G]CCTCATGTCAGGAGA | 25853 |
rs751946649 | snp | A/G | 3.40426e-05 | 0.00412554 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098301 | GAGGAATACACGTCA[A/G]GGATCCCTACACAAG | 25853 |
rs752084826 | snp | C/T | 3.29739e-05 | 0.00406028 | missense | DCAF12 | GRCh38.p7 | 9:34089521 | TGAGCTCGGATGTCA[C/T]AGAACAGCAGGGAGC | 25853 |
rs752109438 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104114 | TCTCTACCAAAAATA[C/T]AAAAATTAGGCACAG | 25853 |
rs752114406 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107461 | AGAAGGATTCAGCTC[A/G]ATGGCATGGATACCA | 25853 |
rs752140154 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112447 | AAAAATACAAAAATC[-/A]GCCAGGTGTGGTGGC | 25853 |
rs752140763 | snp | A/G | 9.14804e-05 | 0.00676253 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107608 | GAACATAAATTTAAC[A/G]TGGCCAATACAGGGT | 25853 |
rs752268354 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090234 | ACACTCAGCTAATTC[C/T]TGCATTTTCAGGAGA | 25853 |
rs752321162 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115436 | CTCTACTAAAAATAC[-/A]AAAAATTAGCCGGGC | 25853 |
rs752372983 | snp | A/C/G | 5.31749e-05 | 0.00515608 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126483 | GGCGGGGGAAGCGAA[A/C/G]GATAGCAGGACGGCG | 25853 |
rs752561913 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121217 | CAAAAAGATCAAACA[A/T]CCCCTTAACCTGGCT | 25853 |
rs752601145 | in-del | -/G | 2.0834e-05 | 0.00322747 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106510 | CTTGGAGAGCAGGGA[-/G]TAACAGGTACAGGGA | 25853 |
rs752659554 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115461 | CCGGGCGGCTGGGCA[C/T]GGTGGCCTGCACCTG | 25853 |
rs752692432 | in-del | -/ACA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106229 | TTCTGAGTATCTGGG[-/ACA]ACAAGTATGCAGTAC | 25853 |
rs752724472 | snp | A/G | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086129 | TGTAACAGAAGTAAC[A/G]TCACACTACTTCAGT | 25853 |
rs752725051 | snp | C/G | 5.91401e-05 | 0.00543751 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106395 | TCTAGCCCCCAATCC[C/G]TGCCACATCAAAAGC | 25853 |
rs752766405 | snp | C/G | 1.67318e-05 | 0.00289234 | missense | DCAF12 | GRCh38.p7 | 9:34088405 | GGGAGGGGACCTCCT[C/G]CCACAAAGAGTTTCG | 25853 |
rs752883456 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118241 | CGGGTTCAAGCGACT[A/G]TCCTGACTCAGACTC | 25853 |
rs752934564 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125135 | AGGAGACTGGGAAGT[A/T]GCTGTGCTGCATAAC | 25853 |
rs753022618 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125228 | TATACTAAGGATCTC[C/T]TCACAGGAGGAAGTC | 25853 |
rs753046982 | snp | A/G | 0.000100595 | 0.00709137 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093492 | GCATCAGCAGAGAGG[A/G]TAAGGCAGGGATATT | 25853 |
rs753066291 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107333 | AAACAAGGCTCCCTC[A/C]AACTACAACTACTGG | 25853 |
rs753113027 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106220 | GCCTCAACCTTCTGA[A/G]TATCTGGGACAACAA | 25853 |
rs753157740 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094264 | ACCAAAAATTAGCTA[A/G]GGGTAGTGGTGCATG | 25853 |
rs753231364 | snp | A/T | 1.64825e-05 | 0.00287071 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107327 | GTTTAAAAACAAGGC[A/T]CCCTCCAACTACAAC | 25853 |
rs753247866 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114319 | TGTAATCCCAGTACT[C/T]TGGGAGTCTGAGGCT | 25853 |
rs753248027 | in-del | -/ATC | 6.69512e-05 | 0.00578542 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096811 | AAACCAGGTTATATT[-/ATC]ATCATCTATAGCAAC | 25853 |
rs753403383 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115986 | CCAAATTTTTAGTAA[C/T]ACAAAACATGGCAAT | 25853 |
rs753411532 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126688 | CTGCAAGGACGGCGA[A/G]CGGCTAGAACCAAAA | 25853 |
rs753417804 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107441 | CCAGTGGCTAGCAGT[G/T]TTCTAGAAGGATTCA | 25853 |
rs753429524 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095673 | GGATTACAGGCCTAA[C/G]GTATTGTGCCCAACT | 25853 |
rs753532503 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102014 | AGTGAGACCCTGTCG[-/C]AAAAAAAAAAAAAAG | 25853 |
rs753566624 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121670 | CTCTTTTCGGCCAGG[C/T]GCGGTGGCTCATGCC | 25853 |
rs753692113 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122836 | ACAGTTGGTTAAAGT[C/G]AAGAATGCCTTCTGT | 25853 |
rs753708891 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102365 | AGCAAACAATAATAA[A/G]GCACTTAAAAACCCA | 25853 |
rs753777097 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115663 | AGTCTCCCCATAGAC[-/AT]ATATATATAGCTTGT | 25853 |
rs753831398 | snp | A/G | 1.65809e-05 | 0.00287926 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34098336 | TACCTTGTTCTTGTT[A/G]TTGAAGGCCAGAGCC | 25853 |
rs753870584 | snp | G/T | 4.89129e-05 | 0.0049451 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126473 | AGCCACATGGGGCGG[G/T]GGAAGCGAAGGATAG | 25853 |
rs753905498 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097619 | TAAGACTTAGTGGAA[A/G]TGTGAAGGGAAAGTA | 25853 |
rs754061753 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110629 | CAGACTTTGGAAGGC[C/T]GAGAAAGAAGTATTA | 25853 |
rs754104092 | snp | C/G | 3.37601e-05 | 0.0041084 | missense | DCAF12 | GRCh38.p7 | 9:34088397 | GCCCTGAAGGGAGGG[C/G]ACCTCCTGCCACAAA | 25853 |
rs754159188 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105399 | CCACTGCACTCCAGC[A/C]TGGGTGACAGAGCAA | 25853 |
rs754192562 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118101 | TATTTCTTCCTACCT[A/T]TAGAAGATGGAAATT | 25853 |
rs754197647 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125100 | TATTAAGGGTCCCAA[A/G]GTGAAACTCTCTCTC | 25853 |
rs754260641 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096444 | TCCTACTAAAAATAC[-/A]AAAAAAAATACCTGG | 25853 |
rs754261955 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | DCAF12 | GRCh38.p7 | 9:34093357 | TCCAAGAAGGAGACA[G/T]GAGCTTGGGAGCCCA | 25853 |
rs754283761 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125198 | TGTAGCCTGACTTCC[C/T]GGTTCTTCAAGTAGT | 25853 |
rs754352768 | snp | G/T | 1.66721e-05 | 0.00288717 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093486 | ACCATGGCATCAGCA[G/T]AGAGGGTAAGGCAGG | 25853 |
rs754573831 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088760 | AGGAGACTTAGAACC[A/G]AAGTTCTGTTTTCCC | 25853 |
rs754584131 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104007 | GGCGCAGTGGCTCAC[A/G]CCTGAAATTCCAGCA | 25853 |
rs754618279 | snp | A/C | 1.94922e-05 | 0.00312182 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126328 | CCTCAGCCTCACCAC[A/C]CAGGTGCCGGCCTCT | 25853 |
rs754677615 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097221 | CAGATTCTGGAGAAG[A/C]CTTTCTCTGGCTCTG | 25853 |
rs754805113 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099999 | CCTCTAGAGCAGTGG[C/T]ACTTAACCTTTTTTG | 25853 |
rs754848458 | snp | C/T | 1.94271e-05 | 0.0031166 | synonymous-codon, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126417 | CCGCTTCCTGCTAAC[C/T]ACTTTCCGGGCCATA | 25853 |
rs754906127 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34098360 | CAGAGCCCGAACCTT[A/G]CAGTTGTCAGGGTTT | 25853 |
rs754998037 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090126 | TGGAGTGCAATGGCG[C/T]GATCTTGGCTCGCTG | 25853 |
rs754998530 | in-del | -/CAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091325 | GAGCAAGACTCATCT[-/CAA]CAACAACAACAACAA | 25853 |
rs755013488 | snp | A/G | 3.6062e-05 | 0.00424614 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088300 | ATCAAAAGAAACAAG[A/G]AAACTGAGAATGGAA | 25853 |
rs755073905 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098774 | AATTTATTTATTATT[A/T]TTATTTTTTTTTGAG | 25853 |
rs755110849 | in-del | -/AAAAAACACCCTAAAAAAAAAAAAAAAAAAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120222 | AAAAAAAAAAAAAAA[lengthTooLong]AAAAAAAAAAAGGCC | 25853 |
rs755144037 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107233 | TTGCCCCTTTATCAA[A/T]TATACACTGTGCCCT | 25853 |
rs755197963 | in-del | -/ACAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102660 | TCTCAAAACAAACAC[-/ACAA]ACAAACAACAACAAA | 25853 |
rs755272062 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125108 | GTCCCAAGGTGAAAC[C/T]CTCTCTCCTTCAGGA | 25853 |
rs755283581 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106077 | TTCTTACAATAAATG[C/T]GTATCACTTTTACAC | 25853 |
rs755321913 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091892 | TGTTCCCCCATCAAG[C/G]TGTGTGATGCTGGGC | 25853 |
rs755331019 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102649 | CAGAGACTCCATCTC[A/G]AAACAAACACACAAA | 25853 |
rs755338793 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34093371 | ATGAGCTTGGGAGCC[C/T]ACTGCATAAACTGAC | 25853 |
rs755447044 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118109 | CCTACCTATAGAAGA[C/T]GGAAATTGATTTATT | 25853 |
rs755499036 | snp | C/G | 8.37752e-05 | 0.00647152 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093490 | TGGCATCAGCAGAGA[C/G]GGTAAGGCAGGGATA | 25853 |
rs755510581 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105405 | CACTCCAGCCTGGGT[A/G]ACAGAGCAAGACCCT | 25853 |
rs755527374 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114420 | ATCCAAAAATTAGCT[A/C]AACTAAGAGTGTGCC | 25853 |
rs755684555 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112823 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGA | 25853 |
rs755718718 | snp | C/T | 8.25171e-05 | 0.00642275 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107311 | TTAATCACTGAGACC[C/T]GTTTAAAAACAAGGC | 25853 |
rs755791061 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124219 | TGACATTACTTGTCC[A/G]TTCACACAGGGGAGG | 25853 |
rs755813514 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088470 | ATTGGGGAAGAAGTC[A/G]ATGTCTGAAAAGTAA | 25853 |
rs755903546 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119551 | TATTTACTTAAGTAT[A/T]CGATTGTTAGTATTT | 25853 |
rs756059807 | snp | C/T | 1.90831e-05 | 0.00308888 | synonymous-codon, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126408 | GGGCGCTTTCCGCTT[C/T]CTGCTAACTACTTTC | 25853 |
rs756145784 | snp | G/T | 1.67719e-05 | 0.0028958 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098316 | GGGATCCCTACACAA[G/T]TTCATACCTTGTTCT | 25853 |
rs756176925 | in-del | -/AGAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107081 | ACAACGCCTAGCCAT[-/AGAA]GACTCAATAAATGCC | 25853 |
rs756246533 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096276 | CTCAGCTACTTGGGA[A/G]GCTGAGGCAAGAGGA | 25853 |
rs756469148 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107063 | TTCACTGCTATGTCT[C/G]AAACAACGCCTAGCC | 25853 |
rs756470499 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104246 | GGGCGACAGAGCGAG[A/G]CTCTGTCTCAAAAAT | 25853 |
rs756564105 | snp | C/T | 1.64898e-05 | 0.00287135 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093248 | AGAACCCATATGCAG[C/T]GCAGCTGTAGGCCTG | 25853 |
rs756622123 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116171 | AAGACCAGCCTGGCA[A/G]ACATGGCAAACCCTG | 25853 |
rs756625241 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126372 | CGGGCCCTGAGCGTC[A/G]CTCCCAGCTCCCGGC | 25853 |
rs756792182 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123887 | GTTCTGTGGAGGCCC[A/G]TTGCCACCACTTAGT | 25853 |
rs756878130 | snp | A/G | 0.000121618 | 0.00779705 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127219 | GCACAACCAACCCAG[A/G]CCGCCCTACGAGTCT | 25853 |
rs756982062 | snp | A/G | 2.2837e-05 | 0.00337905 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106424 | GCTCCCTATAAAAGG[A/G]CAACTTTACCAGACA | 25853 |
rs757090829 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111861 | AAGCATGGGCCAGGC[A/G]CAGTGGCTTATGCCT | 25853 |
rs757099085 | in-del | -/CA | 8.35946e-05 | 0.00646454 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125645 | CCCCCTTCTCCCTCT[-/CA]GTCTGTACTCCCACT | 25853 |
rs757145414 | in-del | -/AAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116670 | CAAGGTTCTGCCTCA[-/AAT]AATAATAATAAATTA | 25853 |
rs757168488 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125256 | GTCTTTTCCTTTTGT[A/G]AAGCGAGTGATCCCA | 25853 |
rs757219157 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112696 | CTGAGGTTGGGAGTT[C/T]GAGACCAGCCTGACC | 25853 |
rs757285469 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119285 | GTTTATTGTACAAAC[A/G]ATACTTTATCAACAA | 25853 |
rs757316925 | snp | C/T | 1.69867e-05 | 0.00291429 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096684 | TGTAAGGTGAATTAT[C/T]AGGTAAAACCACAAA | 25853 |
rs757340461 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121423 | TCCAGCACTCTTACC[A/G]AGAGGTCCCTCGCTC | 25853 |
rs757400995 | snp | A/G | 0.000121426 | 0.00779089 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125586 | TTGAAGGAAATGAGA[A/G]GTAGAGTGATTCCCA | 25853 |
rs757412205 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107779 | ATAGCAATAATATGC[C/T]ACATGAACACAGATT | 25853 |
rs757431213 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119375 | TTTCATTTGTCAGGT[G/T]CCTGTTTAGTCTTCA | 25853 |
rs757465556 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094826 | TGAGCCACCGCACCC[A/G]GCCCCGATTTTTAAA | 25853 |
rs757566546 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109905 | TGTGAGCTGGTGGAC[A/G]GAGAGGGTGACATTG | 25853 |
rs757591629 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107413 | GATGGCAAGACTGTT[A/G]GGGTTGTCTCCTCCA | 25853 |
rs757770355 | snp | C/T | 1.65231e-05 | 0.00287424 | missense | DCAF12 | GRCh38.p7 | 9:34089549 | AGCCCTGCCCTGTTC[C/T]CACAGTGATGATGTG | 25853 |
rs757778249 | snp | C/T | 1.83434e-05 | 0.00302843 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107609 | AACATAAATTTAACG[C/T]GGCCAATACAGGGTA | 25853 |
rs757861930 | snp | C/G | 3.30087e-05 | 0.00406242 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093238 | ACTGAAAGTCAGAAC[C/G]CATATGCAGTGCAGC | 25853 |
rs757872887 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096123 | CACTTCGGGAGACCA[A/G]GGTGGGAGGATCGCT | 25853 |
rs757916743 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090249 | TTGCATTTTCAGGAG[A/G]GACAGGGTTTCACCA | 25853 |
rs757931431 | in-del | -/CACA | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088264 | AAAACACAAGAGCCT[-/CACA]CAATTAGGAAAAAAA | 25853 |
rs757991006 | in-del | -/AG | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098792 | ATTTTTTTTTGAGAC[-/AG]AGTCTCGCTTTGTCA | 25853 |
rs757995089 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116087 | ATAAATCCAGGGCTG[A/G]GTGCGGTGGCTCACG | 25853 |
rs758054870 | snp | A/G | 2.02227e-05 | 0.00317977 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126427 | CTAACTACTTTCCGG[A/G]CCATAGTGGGCAGCG | 25853 |
rs758078022 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104155 | CTGTAGTCCCAGCTA[C/T]TTGGGAGGCCGAGGC | 25853 |
rs758206949 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111733 | GCTAGATTGGACTAG[A/G]CCATTCAGATTCTTT | 25853 |
rs758226970 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122907 | TAGCAAACTTTTCTT[C/T]ACTTAGCTTTTCTGT | 25853 |
rs758240223 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098823 | ACCCAGGCTGGAGTG[C/T]AGTGGTGCGATCTCA | 25853 |
rs758267274 | in-del | -/T | 1.64732e-05 | 0.0028699 | frameshift-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107483 | TGGATACCACAGCCC[-/T]GCTGGGTCACACCTC | 25853 |
rs758270056 | snp | A/G | 1.66382e-05 | 0.00288424 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088410 | GGGACCTCCTGCCAC[A/G]AAGAGTTTCGTTCCA | 25853 |
rs758345985 | snp | C/T | 1.8026e-05 | 0.00300211 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088311 | CAAGGAAACTGAGAA[C/T]GGAAGTTAGTGTAAA | 25853 |
rs758368695 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123827 | AGTGACAAGGATGAC[A/C]GTTCTTAACCACGAG | 25853 |
rs758418779 | snp | C/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086411 | ATAATTTTTATTTTT[C/T]TCCTTGGCAAAAAGT | 25853 |
rs758454421 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125141 | CTGGGAAGTTGCTGT[A/G]CTGCATAACCATGCA | 25853 |
rs758521183 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118259 | CTGACTCAGACTCCC[A/G]AGTAGCCGGGACCAC | 25853 |
rs758660186 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34125336 | TCAGAACAGATCCTA[C/T]TGTATTACAGAAATC | 25853 |
rs758708140 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117138 | GAATTCTGATGTTTC[A/G]CCACAGAATCATGAC | 25853 |
rs758712262 | snp | A/G | 1.68117e-05 | 0.00289923 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093495 | TCAGCAGAGAGGGTA[A/G]GGCAGGGATATTGTT | 25853 |
rs758726401 | in-del | -/AAAT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116371 | ATAAATAAATAATAC[-/AAAT]AAATAAATAAATCTG | 25853 |
rs758741609 | snp | C/G | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086131 | TAACAGAAGTAACGT[C/G]ACACTACTTCAGTAC | 25853 |
rs758889951 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106350 | GCCCGGCTGGGCTGT[C/T]TCCTATCACACTACT | 25853 |
rs758946741 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110059 | TATAATATATGTTTA[A/T]TAAAGACAGAGAGAG | 25853 |
rs758964406 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116050 | TTAGTACTGGGGAAT[A/G]AGGAGGAACAAAATT | 25853 |
rs759053828 | in-del | -/AAGT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103432 | AGAAACAAAAATAAA[-/AAGT]AAGTTTATATTCCCA | 25853 |
rs759123603 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127983 | TGTCCCTTTAGAGAT[A/G]TGCACATAGTGAGTG | 25853 |
rs759133447 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116681 | CTCAAATAATAATAA[A/T]AAATTAATAAATAAA | 25853 |
rs759171862 | snp | C/T | 1.76229e-05 | 0.00296835 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107596 | GATACAGAAGCTGAA[C/T]ATAAATTTAACGTGG | 25853 |
rs759196193 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125058 | ACACCACTTGCCTAT[A/G]ATTCAACCACTGAGA | 25853 |
rs759199769 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | DCAF12 | GRCh38.p7 | 9:34093292 | GACTCTTACCACTGC[C/T]TCGCTCCCTGGAACA | 25853 |
rs759234362 | snp | A/C | 3.81439e-05 | 0.00436698 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089630 | AGTGAGGCGGGAGAG[A/C]ATATTTGCTGACTGT | 25853 |
rs759346264 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091042 | ATAATTAAGAACAAA[C/T]AGGCCAGGCGTGGTG | 25853 |
rs759384003 | snp | A/G | 0.000123209 | 0.00784788 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126474 | GCCACATGGGGCGGG[A/G]GAAGCGAAGGATAGC | 25853 |
rs759474804 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092604 | GGCAGGAGAATCACT[G/T]GAACTCAGAAGGCAG | 25853 |
rs759572138 | snp | C/T | 4.94181e-05 | 0.00497057 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107466 | GATTCAGCTCGATGG[C/T]ATGGATACCACAGCC | 25853 |
rs759575757 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100105 | AGTGGCACAATCATA[G/T]CTCACTGCAGGCTCA | 25853 |
rs759598824 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112497 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 25853 |
rs759624402 | snp | G/T | 3.05283e-05 | 0.00390682 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106384 | CCTTTTCAATCTCTA[G/T]CCCCCAATCCCTGCC | 25853 |
rs759693070 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095872 | GTAGTCATCAATCTA[C/T]AAAGAAATACTTAAA | 25853 |
rs759734122 | snp | A/C | 0.00113407 | 0.0237855 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088398 | CCCTGAAGGGAGGGG[A/C]CCTCCTGCCACAAAG | 25853 |
rs759823932 | snp | A/C | 1.64779e-05 | 0.00287031 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088531 | AAGAGAAAGAGACTA[A/C]AATTAGCACCTCTAG | 25853 |
rs759877697 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087543 | TTTAGGGGTGTGGCT[A/G]CTGGCTAAGCAGATG | 25853 |
rs759984814 | snp | A/G | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086060 | GCAAGCACTTTCAGC[A/G]TCATTCTCAGGGCAC | 25853 |
rs760032671 | in-del | -/GAG | | | cds-indel | DCAF12 | GRCh38.p7 | 9:34086701 | TCTAGGTTCGAAGAT[-/GAG]AATTCCAGAACCTGT | 25853 |
rs760099412 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126648 | GAAGGGGAAGCGAGA[A/G]TGAGCGGCTTTCCGA | 25853 |
rs760122203 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095577 | ATTTTGTTGCAGAGA[C/T]AGGGTCTTACTGTGT | 25853 |
rs760152347 | in-del | -/GTAAAACCACAAAATCATGTTCATCA | 1.6981e-05 | 0.00291379 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096686 | AAGGTGAATTATTAG[-/GTAAAACCACAAAATCATGTTCATCA]GTAAAACCACAAAAT | 25853 |
rs760186338 | snp | A/G | 1.71299e-05 | 0.00292654 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098288 | AAGACATAAGCAAGA[A/G]GAATACACGTCAGGG | 25853 |
rs760280831 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122950 | CAATCTGAATTTGCG[-/T]TAAGTCTAAACCATG | 25853 |
rs760341050 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094692 | CCCACCACCACGCCC[A/G]GCTAATTTTTTGTAT | 25853 |
rs760344740 | snp | A/C | 1.70568e-05 | 0.0029203 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107577 | ATAGCTACAAGAAAA[A/C]ATGGATACAGAAGCT | 25853 |
rs760441039 | snp | A/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127911 | CCATCCCAAGTCGGC[A/T]CTACCACTAACCCCT | 25853 |
rs760452794 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090014 | AAATCATTAAGTCAT[C/T]AACGATTCCTTATAT | 25853 |
rs760487029 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103952 | CCCTTCCCACACTGC[C/T]AATCTCCTGAACACT | 25853 |
rs760492457 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103611 | GTAATCCCAGCACTT[C/G]GAGAGGCTCAAGTGG | 25853 |
rs760507782 | snp | C/T | 1.64836e-05 | 0.0028708 | missense | DCAF12 | GRCh38.p7 | 9:34089512 | AGAAATCTCTGAGCT[C/T]GGATGTCATAGAACA | 25853 |
rs760613785 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104706 | GGATCAACTGAGGTC[C/T]TGCATTCAAGACCAG | 25853 |
rs760726475 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115892 | ACTACATACCTTTAA[C/T]GGCGATAAGGTAGTT | 25853 |
rs760731299 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123714 | TATGATGATTAATTC[A/C]GTTTACAATTCAGTA | 25853 |
rs760784395 | snp | A/G | 2.37985e-05 | 0.00344945 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126469 | CCGCAGCCACATGGG[A/G]CGGGGGAAGCGAAGG | 25853 |
rs760792360 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110539 | CCATGCCAGTCCCCA[A/G]CTAAAAAACATCCAA | 25853 |
rs760867237 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111320 | CAACATGTACTTATC[A/T]TTCATGATTCGGTTC | 25853 |
rs760874548 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34098444 | AGGGACCCGTGACAC[A/G]TTGTGTCTCGCATCA | 25853 |
rs760892945 | snp | C/T | 1.75798e-05 | 0.00296472 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098557 | GTCAGATGTACCCAC[C/T]CCTCTATGGGAAATC | 25853 |
rs760895052 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122633 | AGGCACCCACCATCA[G/T]GCCCAGCTAATTTGT | 25853 |
rs760907256 | snp | C/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086470 | TCTCAAACAATCAAA[C/T]GCATTACCCATTACA | 25853 |
rs761052727 | snp | A/G | 0.000458416 | 0.0151327 | missense | DCAF12 | GRCh38.p7 | 9:34088393 | TGGAGCCCTGAAGGG[A/G]GGGGACCTCCTGCCA | 25853 |
rs761100110 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125183 | TAGCTGGTTTCATTC[C/T]GTAGCCTGACTTCCC | 25853 |
rs761120078 | in-del | -/TC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096133 | ACCAAGGTGGGAGGA[-/TC]TCGCTTGAGGTCAGG | 25853 |
rs761178333 | snp | C/T | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34085945 | TCTAGAAGAGCATCA[C/T]TCACTGTGGTCACTG | 25853 |
rs761190056 | snp | C/G | 0.000315617 | 0.0125582 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093477 | AGAGATATAACCATG[C/G]CATCAGCAGAGAGGG | 25853 |
rs761232516 | snp | A/G/T | 0.000181202 | 0.00951693 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125093 | AACACTTTATTAAGG[A/G/T]TCCCAAGGTGAAACT | 25853 |
rs761414178 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120397 | ACAAAGTGGCTGGGC[A/G]TGGTGGCTCACGTTT | 25853 |
rs761504714 | snp | A/G/T | 3.32161e-05 | 0.00407519 | missense | DCAF12 | GRCh38.p7 | 9:34096726 | CACACCTTAGATAGT[A/G/T]TATTTTCAGCCTTCC | 25853 |
rs761658919 | snp | A/G | 2.28485e-05 | 0.0033799 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106530 | AGGTACAGGGAGGAA[A/G]ATAAGAAATTAGTAA | 25853 |
rs761716535 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095294 | TGGCCAGCATGGTCT[C/T]AATCTCTTGACCTCA | 25853 |
rs761725645 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104035 | GCACTTTGGGAGGCC[A/G]ATGCAGGCAGATCAC | 25853 |
rs761778757 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113208 | AGGTGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 25853 |
rs761810533 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089843 | AAGTGTCAGATTCCC[A/G]ATGATGCTCAAGATG | 25853 |
rs761820325 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107393 | TCCAGCGTAGGTAGT[C/T]GATAGATGGCAAGAC | 25853 |
rs761849168 | snp | A/G | 1.87778e-05 | 0.00306407 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126394 | GCTCCCGGCGAGGCG[A/G]GCGCTTTCCGCTTCC | 25853 |
rs761928345 | snp | C/G | 1.86114e-05 | 0.00305047 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126388 | CTCCCAGCTCCCGGC[C/G]AGGCGGGCGCTTTCC | 25853 |
rs761936658 | snp | A/T | 1.72579e-05 | 0.00293746 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089596 | GACCGGATTCCTGAA[A/T]GACAGAAAAGTAAAA | 25853 |
rs761944029 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121428 | CACTCTTACCGAGAG[C/G]TCCCTCGCTCTCTTA | 25853 |
rs761944305 | snp | A/T | 1.69602e-05 | 0.00291201 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098305 | AATACACGTCAGGGA[A/T]CCCTACACAAGTTCA | 25853 |
rs762013826 | in-del | -/TT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122473 | AGACATTAGTATCAA[-/TT]TTTTTTTTTTTTTTT | 25853 |
rs762150402 | in-del | -/AGAA | 1.6476e-05 | 0.00287014 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088519 | TGATTCTACGGGAAG[-/AGAA]AGAGACTACAATTAG | 25853 |
rs762188593 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | DCAF12 | GRCh38.p7 | 9:34098436 | GCATACACAGGGACC[C/T]GTGACACATTGTGTC | 25853 |
rs762206862 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097041 | CCCTCAACGTCCTGT[C/T]GGAGAGTTAAAGCAG | 25853 |
rs762283707 | snp | A/C | 1.78061e-05 | 0.00298375 | missense | DCAF12 | GRCh38.p7 | 9:34088353 | GGGGAGTTGTCATTA[A/C]CTCCAGAGCCCAGCA | 25853 |
rs762359428 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105029 | GAGGCCGAGGCAGGC[C/G]AATCACTGAGGTCAG | 25853 |
rs762437469 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110288 | TAACACCACCACTAT[C/T]TACCCTGTCACTCAA | 25853 |
rs762477420 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115320 | ATAGCGGCTAGGCGC[A/G]GTGGCTCACACCTGT | 25853 |
rs762533429 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099404 | GCCCAGTTAATTTTT[A/G]TATTTTTAGTAGAGA | 25853 |
rs762572723 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125171 | AACACTCGAGAGTAG[C/T]TGGTTTCATTCTGTA | 25853 |
rs762580140 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101687 | ATGAGCCACTGTGCC[C/T]GGCCCACAATCCTTC | 25853 |
rs762583566 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120541 | CCAGGCATGGTAGCA[C/T]GCGCCTGTAGTCCCA | 25853 |
rs762658386 | snp | A/C | 1.65614e-05 | 0.00287757 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093466 | GAAAATAGAGGAGAG[A/C]TATAACCATGGCATC | 25853 |
rs762702530 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112665 | GTACTTTGGGAGGCC[A/G]AGGAGGGCGGATCAT | 25853 |
rs762817108 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106975 | ATATTAGTTTATATG[A/G]TTTATGTTTTGTCTA | 25853 |
rs762949620 | snp | A/G | 2.13427e-05 | 0.00326663 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106516 | GAGCAGGGAGTAACA[A/G]GTACAGGGAGGAAAA | 25853 |
rs763023194 | in-del | -/TA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108987 | ATGTATATGTTTTTA[-/TA]TATATATATATATAT | 25853 |
rs763053079 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | DCAF12 | GRCh38.p7 | 9:34089475 | GGGCTTGGACCCATA[A/C]CAAGCTGAGAGCCTC | 25853 |
rs763094197 | snp | C/T | 1.69654e-05 | 0.00291246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125327 | TACTCTTCTTCAGAA[C/T]AGATCCTACTGTATT | 25853 |
rs763174829 | in-del | -/A | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086006 | TATGGTTCCAACTAC[-/A]AAAAAACAAAAATTA | 25853 |
rs763315808 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113469 | CTCAGCCTCCCAAGT[C/T]GCTGGGATGGCAGGT | 25853 |
rs763341102 | snp | C/G | 1.8265e-05 | 0.00302195 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126369 | CTGCGGGCCCTGAGC[C/G]TCGCTCCCAGCTCCC | 25853 |
rs763365456 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109375 | ACAGCTCCTAGATGG[C/T]TGTGTTGTTGCCAAT | 25853 |
rs763431762 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089337 | GTAGATGGTGTGTCA[G/T]TGGGGGCTGAGAGAT | 25853 |
rs763453192 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110161 | AACTGGCAACTACCT[A/G]AGAGCAGCAGACTCC | 25853 |
rs763501013 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109831 | GGCAGCTTTAGGGGT[C/T]GGAAGCAGATGTCTT | 25853 |
rs763504277 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119194 | TTGAGCCCCTACTTC[A/G]GTCCTTCTCACCGTC | 25853 |
rs763557246 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121036 | GCATGTGCCCGTACT[C/T]CCAGCCACTCGGGAG | 25853 |
rs763631249 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125077 | CAACCACTGAGATGC[A/G]AACACTTTATTAAGG | 25853 |
rs763640257 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116336 | GCCTGGGCGACAGAG[A/G]GAGTCCGTCTCAAAA | 25853 |
rs763650270 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | DCAF12 | GRCh38.p7 | 9:34093336 | TTGTATGATGGCTGC[C/T]GTGGATCCAAGAAGG | 25853 |
rs763805779 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117683 | ACTTTGGGAGGCCCA[A/G]GCGGGAGGATCACCT | 25853 |
rs763923720 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123839 | GACAGTTCTTAACCA[C/T]GAGTGGGCAGCTGGA | 25853 |
rs763966458 | snp | C/T | 5.21716e-05 | 0.00510716 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089377 | TAATTTTTCTGTTAC[C/T]GTGTAGCAGTCATCT | 25853 |
rs763968716 | snp | G/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128215 | ACAACCTAGGAACCA[G/T]CCCCAAATGTACCTT | 25853 |
rs764030725 | snp | C/T | 3.31345e-05 | 0.00407016 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088419 | TGCCACAAAGAGTTT[C/T]GTTCCAGACGAGTCG | 25853 |
rs764040595 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102301 | AAAAAAAAAGAATAA[C/T]GACTGTTTTATATAA | 25853 |
rs764063868 | snp | A/G | 2.17318e-05 | 0.00329628 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106521 | GGGAGTAACAGGTAC[A/G]GGGAGGAAAATAAGA | 25853 |
rs764128056 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124898 | ACCAACGGGAAAGAA[C/T]GGAAAGGAGAGTAAG | 25853 |
rs764283299 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089484 | CCCATAACAAGCTGA[A/G]AGCCTCTCTTCCAGA | 25853 |
rs764337097 | snp | C/G | 1.828e-05 | 0.00302319 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126379 | TGAGCGTCGCTCCCA[C/G]CTCCCGGCGAGGCGG | 25853 |
rs764347384 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095983 | TTTAAAAGACTTTCC[C/T]GCAAGAGAGGCACAC | 25853 |
rs764361874 | snp | A/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086461 | AACAGAAAATCTCAA[A/T]CAATCAAACGCATTA | 25853 |
rs764361883 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102338 | TGCTTAAAAAGATAA[A/G]TCAGTTTTCTTAGCA | 25853 |
rs764424376 | snp | A/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087137 | TGCTGACTGCAGGCC[A/T]GCCTGTCACCATCTC | 25853 |
rs764431929 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109827 | TGTGGGCAGCTTTAG[A/G]GGTCGGAAGCAGATG | 25853 |
rs764517948 | snp | C/G | 1.66538e-05 | 0.00288559 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096788 | TCCCAGTTCCTACAA[C/G]AGCAATGAAAACCAG | 25853 |
rs764607915 | snp | A/G | 3.41303e-05 | 0.00413086 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098297 | GCAAGAGGAATACAC[A/G]TCAGGGATCCCTACA | 25853 |
rs764634543 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121055 | GCCACTCGGGAGGCA[C/G]AGGTGAGAGAATCAC | 25853 |
rs764709514 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096302 | GAGGATCGCTTATGC[C/T]CAGGAGTTCAAGGCT | 25853 |
rs764735088 | snp | C/T | 1.9598e-05 | 0.00313028 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089635 | GGCGGGAGAGAATAT[C/T]TGCTGACTGTCTGCT | 25853 |
rs764791049 | snp | C/T | 1.82035e-05 | 0.00301686 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107607 | TGAACATAAATTTAA[C/T]GTGGCCAATACAGGG | 25853 |
rs764815881 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125064 | CTTGCCTATGATTCA[A/G]CCACTGAGATGCAAA | 25853 |
rs764854664 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128029 | AGCTTTCTTTTTTGA[A/G]TCTGTTCTAATTCTG | 25853 |
rs764922147 | in-del | -/AAA | | | cds-indel | DCAF12 | GRCh38.p7 | 9:34088127 | AAAGCCAGAAATAAT[-/AAA]AGATAGTAAAATTTT | 25853 |
rs764926887 | in-del | -/G | 2.07445e-05 | 0.00322053 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106506 | CATCCTTGGAGAGCA[-/G]GGAGTAACAGGTACA | 25853 |
rs764961627 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116802 | CCTGGCCAACATGGC[A/G]AAACGCCATCTCTAC | 25853 |
rs764970375 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | DCAF12 | GRCh38.p7 | 9:34093303 | CTGCCTCGCTCCCTG[A/G]AACAGACAGACTTGA | 25853 |
rs764981100 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116059 | GGGAATAAGGAGGAA[A/C]AAAATTAAATAAATA | 25853 |
rs765083411 | snp | A/G | 2.46746e-05 | 0.00351236 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126475 | CCACATGGGGCGGGG[A/G]AAGCGAAGGATAGCA | 25853 |
rs765110171 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123792 | AACTCTTCCAAGCAG[C/G]AGACTCTTTTTCTAC | 25853 |
rs765111806 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106236 | TATCTGGGACAACAA[A/G]TATGCAGTACCACAC | 25853 |
rs765203748 | snp | C/T | 3.02906e-05 | 0.00389158 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106387 | TTTCAATCTCTAGCC[C/T]CCAATCCCTGCCACA | 25853 |
rs765295908 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090811 | AGGCACCCGCTACCA[C/T]CCCCAGCTAATTTTG | 25853 |
rs765323425 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091152 | GCCAACATGGTGAAA[C/T]TCCATCTCTACTAAA | 25853 |
rs765362430 | snp | C/T | 0.00338499 | 0.0410005 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088401 | TGAAGGGAGGGGACC[C/T]CCTGCCACAAAGAGT | 25853 |
rs765373011 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | DCAF12 | GRCh38.p7 | 9:34088537 | AAGAGACTACAATTA[A/G]CACCTCTAGCCATGG | 25853 |
rs765385085 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111723 | CAGTCCAAAGGCTAG[A/T]TTGGACTAGGCCATT | 25853 |
rs765401689 | snp | A/G | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088102 | GGGATTAGCAACAAT[A/G]TTTGGTTGAAAAGCC | 25853 |
rs765672226 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125223 | AGTAGTATACTAAGG[A/T]TCTCTTCACAGGAGG | 25853 |
rs765679575 | snp | A/C | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087551 | TGTGGCTACTGGCTA[A/C]GCAGATGTGAGGGTG | 25853 |
rs765691331 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109954 | TCCAACACCTTGGGT[A/G]GGGGCATTACACTGG | 25853 |
rs765766345 | snp | A/G | 3.35171e-05 | 0.00409358 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093491 | GGCATCAGCAGAGAG[A/G]GTAAGGCAGGGATAT | 25853 |
rs765784834 | snp | C/G | 3.31554e-05 | 0.00407144 | missense | DCAF12 | GRCh38.p7 | 9:34096760 | GATGAAAGTAGCCAT[C/G]CAGAGACACTGCTCC | 25853 |
rs765830750 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127937 | CCCCTAATGTCTTGC[A/G]AAAGGCAGCTCCATC | 25853 |
rs765897849 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107439 | CTCCAGTGGCTAGCA[A/G]TGTTCTAGAAGGATT | 25853 |
rs765936913 | in-del | -/ACCACAAAATC | 6.75801e-05 | 0.00581253 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096692 | GAATTATTAGGTAAA[-/ACCACAAAATC]ATGTTCATCACACCT | 25853 |
rs765994316 | in-del | -/TT | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34128259 | GATTTCTTTTCTTTT[-/TT]TTTTTTTTTGAGATG | 25853 |
rs766011121 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114173 | AAAAAGAATGAAATC[C/T]TTTGGACAACATGGA | 25853 |
rs766071925 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093138 | ACAGGCGTAAGCCAC[C/T]ACGCCTAGCCATCGC | 25853 |
rs766096633 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126658 | CGAGAATGAGCGGCT[A/T]TCCGACGGCAGAGCC | 25853 |
rs766101770 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096953 | AGAACCTAGCTGAAT[A/G]GCATATTAAATTGAG | 25853 |
rs766115369 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095649 | CTGCTTCAACCTCCC[A/G]AAGTGTTGGGATTAC | 25853 |
rs766263445 | snp | C/G/T | 3.83313e-05 | 0.00437772 | synonymous-codon, missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126410 | GCGCTTTCCGCTTCC[C/G/T]GCTAACTACTTTCCG | 25853 |
rs766345865 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097411 | AGGCATATGCCACCA[C/T]GCCTGGCTAATTTTT | 25853 |
rs766350341 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102761 | TTCTAGAGGACAACT[G/T]AGCAACCTGCAGCAA | 25853 |
rs766354212 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115952 | ATTAATTCCCTATTA[C/T]TGAACATTTATGCCA | 25853 |
rs766411840 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109215 | CAAACTCTCTCTCCT[C/T]CTTGGCTGTGGTATC | 25853 |
rs766461281 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111678 | AGACCCCCTGATCAC[A/G]GCACAGTCTAGAGGG | 25853 |
rs766473310 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090972 | CCTATTTATTCCTTT[C/T]TCTACTACTCTCATT | 25853 |
rs766482206 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103953 | CCTTCCCACACTGCT[A/C]ATCTCCTGAACACTT | 25853 |
rs766507843 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091415 | ACTTTGGGAGGCTGA[A/G]GTGGGTGTCCCAAGA | 25853 |
rs766527159 | in-del | -/A | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086420 | ATTTTTTTCCTTGGC[-/A]AAAAGTCAAGTGCTA | 25853 |
rs766531746 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122701 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 25853 |
rs766575081 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110611 | TAAGACTCTCCTCGG[A/G]GCCAGACTTTGGAAG | 25853 |
rs766623530 | snp | G/T | 1.68946e-05 | 0.00290638 | missense | DCAF12 | GRCh38.p7 | 9:34088396 | AGCCCTGAAGGGAGG[G/T]GACCTCCTGCCACAA | 25853 |
rs766679400 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118026 | CCAAGTGATACCAAT[A/C]TGAAAAATGAAAGGG | 25853 |
rs766712379 | in-del | -/GGGA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34088565 | TGGGGCAGGAAAAGG[-/GGGA]GGAAGGGACAGGAAT | 25853 |
rs766816792 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109907 | TGAGCTGGTGGACGG[A/C]GAGGGTGACATTGTA | 25853 |
rs766843126 | snp | C/T | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34085961 | TCACTGTGGTCACTG[C/T]GTCTTCCCCTTACAA | 25853 |
rs766859805 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125185 | GCTGGTTTCATTCTG[C/T]AGCCTGACTTCCCGG | 25853 |
rs766867805 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098674 | AAACACAGAGCAGTA[A/G]GCATTTTAATAGCTA | 25853 |
rs766905879 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111879 | GTGGCTTATGCCTGT[A/C]ATCCCAGCACTTAGG | 25853 |
rs767087718 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105899 | GACTACAAGCGCCCA[C/T]GACCACACTCAGCTA | 25853 |
rs767133461 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118962 | AGAGTAAGACCCTGT[C/G]TCAAAAAAGAAAATA | 25853 |
rs767193053 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34102051 | ATGACGACTATTCTA[A/G]GCTGGGTACAGTGGT | 25853 |
rs767244956 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123634 | TAGGAATTAAGAGTA[A/G]GTTAAATTATTACTT | 25853 |
rs767388718 | snp | A/G | 6.96727e-05 | 0.00590182 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106531 | GGTACAGGGAGGAAA[A/G]TAAGAAATTAGTAAA | 25853 |
rs767476544 | snp | A/G | 1.71555e-05 | 0.00292873 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089395 | GTAGCAGTCATCTCA[A/G]GTAGGGGCTTACGCA | 25853 |
rs767486773 | snp | C/G/T | 4.94176e-05 | 0.00497059 | synonymous-codon, missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107394 | CCAGCGTAGGTAGTC[C/G/T]ATAGATGGCAAGACT | 25853 |
rs767505215 | snp | C/T | 0.000115379 | 0.00759449 | missense | DCAF12 | GRCh38.p7 | 9:34089506 | TCTTCCAGAAATCTC[C/T]GAGCTCGGATGTCAT | 25853 |
rs767507199 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126631 | ACTTGAGCCGGGAAA[A/G]GGAAGGGGAAGCGAG | 25853 |
rs767564019 | snp | A/C | 0.000121352 | 0.00778853 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125601 | GGTAGAGTGATTCCC[A/C]TACCGACATGGGCTG | 25853 |
rs767592063 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103712 | TAGAAATAATTAACC[A/G]GGTGTGGTGGTGTGT | 25853 |
rs767647050 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089981 | TACACTGCAACTCAA[C/G]GTAATCTGCATATTT | 25853 |
rs767652039 | snp | A/G | 1.86569e-05 | 0.00305419 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126391 | CCAGCTCCCGGCGAG[A/G]CGGGCGCTTTCCGCT | 25853 |
rs767661248 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122570 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 25853 |
rs767663746 | snp | A/C/G | 3.29512e-05 | 0.00405891 | missense | DCAF12 | GRCh38.p7 | 9:34098437 | CATACACAGGGACCC[A/C/G]TGACACATTGTGTCT | 25853 |
rs767720148 | snp | C/T | 1.68826e-05 | 0.00290534 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098309 | CACGTCAGGGATCCC[C/T]ACACAAGTTCATACC | 25853 |
rs767799161 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094212 | GAGTTTGAGACCAGG[C/T]TGGCCAACCTGGTGA | 25853 |
rs767907683 | in-del | -/GAAAAAAAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115436 | TCTACTAAAAATACA[-/GAAAAAAAA]AAAAATTAGCCGGGC | 25853 |
rs767996907 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110352 | TCATTTCCATCATCC[C/T]AGTCCTGCCTAACCT | 25853 |
rs768032385 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091509 | AATGAGGTGGCGGAC[A/G]CTTATAGTCCCAGCT | 25853 |
rs768109717 | snp | A/C | 1.64757e-05 | 0.00287012 | stop-gained, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125178 | GAGAGTAGCTGGTTT[A/C]ATTCTGTAGCCTGAC | 25853 |
rs768288853 | snp | G/T | 3.34566e-05 | 0.00408989 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125304 | ACATTAGAAATCAGG[G/T]CTTTGGCTACTCTTC | 25853 |
rs768296008 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105842 | CAACCTCTGCCTGCC[A/G]GGTTCAAGCAATTCT | 25853 |
rs768318809 | snp | A/T | 3.32718e-05 | 0.00407858 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34096719 | TGTTCATCACACCTT[A/T]GATAGTGTATTTTCA | 25853 |
rs768328348 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095220 | TCTGGGACTACAGAC[A/G]CCCACCACCACGCCC | 25853 |
rs768372574 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099754 | ACACGTCACCATGCC[C/T]GGCTAATTTTTGTAT | 25853 |
rs768490196 | snp | A/G | 1.69069e-05 | 0.00290743 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096831 | TCTATAGCAACTAAT[A/G]TACGATAATAAGCAG | 25853 |
rs768537725 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106987 | ATGGTTTATGTTTTG[C/T]CTATATGTCACCCTC | 25853 |
rs768543997 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119645 | GTGTGAACATTTTAG[A/G]CAAAAGGGTATAACA | 25853 |
rs768591215 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108363 | AATAGATACACCTTA[C/T]AGCCTAAGAGGCTGA | 25853 |
rs768649055 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094052 | AAAGGCTATTGTGAC[A/T]TGAAGGAATCACTAA | 25853 |
rs768755671 | snp | A/G | 3.38181e-05 | 0.00411192 | missense | DCAF12 | GRCh38.p7 | 9:34089585 | AGAAACTCACTGACC[A/G]GATTCCTGAAAGACA | 25853 |
rs768797418 | in-del | -/C | 1.69454e-05 | 0.00291074 | frameshift-variant | DCAF12 | GRCh38.p7 | 9:34088398 | CCTGAAGGGAGGGGA[-/C]CCTCCTGCCACAAAG | 25853 |
rs768907235 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107518 | CTCCCGGTCTTTCAG[A/G]ATGGGGATCTTGGTG | 25853 |
rs768980362 | snp | G/T | 0.000121249 | 0.00778523 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127310 | CCTGATCCTTTCTCC[G/T]GTCCGAAATGCTTCA | 25853 |
rs768992772 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104573 | ATTACTTTGTGTACA[A/G]TGTGACCTCATTTAC | 25853 |
rs768992955 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118250 | CGACTGTCCTGACTC[-/A]AGACTCCCGAGTAGC | 25853 |
rs769064349 | snp | A/G | 1.67789e-05 | 0.00289641 | missense | DCAF12 | GRCh38.p7 | 9:34098512 | CCATAGAACCATCAC[A/G]TGAGCCTGCAGGGCC | 25853 |
rs769117701 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123380 | TCAGAATATTTCCCA[A/G]ATGCATGCAGACACC | 25853 |
rs769123972 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110192 | CTGCCTAACTGGCAT[C/G]ATTGCTGATGCATCC | 25853 |
rs769125170 | snp | A/C | 8.99078e-05 | 0.00670417 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126455 | GCGCCGCCGCGGCCC[A/C]GCAGCCACATGGGGC | 25853 |
rs769139139 | snp | A/G | 9.88386e-05 | 0.00702919 | missense | DCAF12 | GRCh38.p7 | 9:34098419 | CCTTGTGAGTGATGT[A/G]TGCATACACAGGGAC | 25853 |
rs769309926 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120185 | TTCAGCCTGGGCAAC[A/T]AGAATGAAAGTCCGT | 25853 |
rs769315422 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111231 | CCTTGTGATCCACCT[G/T]CCTCAGCCTCCCAAA | 25853 |
rs769339456 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099391 | CGCGTGCCACCACGC[C/T]CAGTTAATTTTTGTA | 25853 |
rs769348359 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | DCAF12 | GRCh38.p7 | 9:34098396 | TTCTTTGGGGATGTC[C/G]TTTAAGGCCTTGTGA | 25853 |
rs769351048 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122371 | CAATCCTTACTCTCT[A/G]CCAAGCTTCAACTAA | 25853 |
rs769368987 | snp | C/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086962 | AGAGGAACTGGTGGG[C/T]GGGAACAGCTGTTAT | 25853 |
rs769373472 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120454 | GGCGGGCAGATTACA[C/T]GAGGTCAGGCGTTTG | 25853 |
rs769448472 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106664 | ATGATCAATCTTTAC[C/G]TTCTATCTTGAGGAG | 25853 |
rs769469263 | snp | C/T | 3.57788e-05 | 0.00422944 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088344 | TCTGCATTTGGGGAG[C/T]TGTCATTAACTCCAG | 25853 |
rs769628288 | snp | C/T | 1.65781e-05 | 0.00287902 | splice-acceptor-variant | DCAF12 | GRCh38.p7 | 9:34125279 | TGATCCCAGCCAAAC[C/T]GTGGAAACAACATTA | 25853 |
rs769717651 | snp | A/C/T | 3.34578e-05 | 0.00408999 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096707 | ACCACAAAATCATGT[A/C/T]CATCACACCTTAGAT | 25853 |
rs769837877 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107367 | AACTTACATCTCCTA[C/T]ACACACAGGATCCAG | 25853 |
rs769840502 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113644 | CGCACCAAGGCTGAA[A/T]TTTCTTTAAAAAACA | 25853 |
rs769850148 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124730 | TATGACTTAAAAACC[A/T]GCATAAAAATATGAG | 25853 |
rs769871213 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093862 | GCTGATCTCTGGCTA[-/C]CCCCCAGCTCACCTT | 25853 |
rs769970332 | snp | A/T | 2.04275e-05 | 0.00319583 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106500 | TGTGTCCATCCTTGG[A/T]GAGCAGGGAGTAACA | 25853 |
rs770013048 | in-del | -/TTTTTTTT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095375 | ACCGCGCCAGGCCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 25853 |
rs770078746 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113224 | GCCCGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 25853 |
rs770095268 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093885 | CTCACCTTCCCACCT[C/G]AATGGGAATTGTACG | 25853 |
rs770108484 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090461 | AGTCATGTAATTACT[A/T]TAGATCACAAGGAAA | 25853 |
rs770119645 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126108 | CTTTTCAAGCCCTAT[C/T]CACGAATGCAGGCCT | 25853 |
rs770142341 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095018 | TCAGAAAGCAAAGGT[A/G]TCCCATGTGAAATTT | 25853 |
rs770363311 | snp | C/T | 5.50131e-05 | 0.00524438 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126362 | CCCTCACCTGCGGGC[C/T]CTGAGCGTCGCTCCC | 25853 |
rs770459144 | snp | A/C | 4.34962e-05 | 0.00466328 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126444 | CATAGTGGGCAGCGC[A/C]GCCGCGGCCCCGCAG | 25853 |
rs770459296 | snp | G/T | 1.71143e-05 | 0.00292521 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098292 | CATAAGCAAGAGGAA[G/T]ACACGTCAGGGATCC | 25853 |
rs770475452 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101162 | TTGTAGCCTCAACCT[C/T]CTGGGCTTCAGCAAT | 25853 |
rs770499092 | snp | A/G | 1.79686e-05 | 0.00299733 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088332 | TTAGTGTAAATCTCT[A/G]CATTTGGGGAGTTGT | 25853 |
rs770571008 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121667 | GCCCTCTTTTCGGCC[A/C]GGCGCGGTGGCTCAT | 25853 |
rs770639188 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121885 | GAGGCAGAGGTTGCA[A/G]TGAGCTGAGATCGCG | 25853 |
rs770686978 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125054 | CCACACACCACTTGC[C/G]TATGATTCAACCACT | 25853 |
rs770711560 | snp | C/G | 4.94262e-05 | 0.00497098 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093279 | AGGTGCACACAGGGA[C/G]TCTTACCACTGCCTC | 25853 |
rs770716160 | snp | C/T | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34087326 | AACCCACTGGGGAGA[C/T]TGGAAGAATGGCAGA | 25853 |
rs770796112 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107669 | ACATTTAATTAACAA[C/T]TACTACATGTTAGAC | 25853 |
rs770830876 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125154 | GTGCTGCATAACCAT[C/G]CAACACTCGAGAGTA | 25853 |
rs770977107 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124611 | AAAACAGCCAAGTGT[A/G]CTATTTTAAATACTT | 25853 |
rs771037840 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111273 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCCTCTCC | 25853 |
rs771038838 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089110 | GAGTGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs771058177 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116505 | GTGAATGAAACCCTG[C/T]CTCCATTAAAAATAC | 25853 |
rs771149984 | in-del | -/CTTT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095083 | TTTGGACTTTGGAGG[-/CTTT]TTTTTTTGAGAGAGA | 25853 |
rs771177118 | snp | A/T | 2.00479e-05 | 0.003166 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106489 | GATCCAGTCCTTGTG[A/T]CCATCCTTGGAGAGC | 25853 |
rs771198620 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092515 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25853 |
rs771296669 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101880 | AATTAGCCAGGCGTG[C/G]TGGGGCACGCCTGTG | 25853 |
rs771302661 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112453 | ACAAAAATCAGCCAG[C/G]TGTGGTGGCGTGAGT | 25853 |
rs771338520 | snp | A/C/G | 3.29534e-05 | 0.00405904 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107335 | ACAAGGCTCCCTCCA[A/C/G]CTACAACTACTGGGA | 25853 |
rs771426594 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | DCAF12 | GRCh38.p7 | 9:34089459 | TCTCCCCTGCTAGTC[C/T]GGGCTTGGACCCATA | 25853 |
rs771451419 | snp | C/T | 1.67916e-05 | 0.0028975 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125311 | AAATCAGGGCTTTGG[C/T]TACTCTTCTTCAGAA | 25853 |
rs771453986 | in-del | -/ATCA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103047 | GTGAGCCATGATCAC[-/ATCA]CGCCACTGCATTCCA | 25853 |
rs771525910 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113311 | CCTGCTTTGGCCTCC[A/G]AAAGTGCTGGGATTA | 25853 |
rs771580984 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121771 | AACACGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 25853 |
rs771647962 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | DCAF12 | GRCh38.p7 | 9:34098379 | TTGTCAGGGTTTGTG[C/T]CTTCTTTGGGGATGT | 25853 |
rs771680472 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120336 | AGTGAGCCATGACTG[A/C]ACCACTGTACTCCAC | 25853 |
rs771763243 | snp | A/C | 3.71257e-05 | 0.0043083 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126348 | TGCCGGCCTCTCAAC[A/C]CTCACCTGCGGGCCC | 25853 |
rs771835961 | in-del | -/TGTAGT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122848 | GTCAAGAATGCCTTC[-/TGTAGT]TGTAGTTCTTTGCAG | 25853 |
rs771899353 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113143 | ACAACCTCTGCCTCC[C/T]GGGTACAAGCAATTC | 25853 |
rs771945952 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095455 | GCAAAATTACGGCTC[A/G]CTGCAGCCTTGACCT | 25853 |
rs771947912 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109884 | AAAGGTCTCGTCTGT[A/G]TTTTCTGTGAGCTGG | 25853 |
rs772047588 | in-del | -/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095083 | TTTGGACTTTGGAGG[-/C]TTTTTTTTTTGAGAG | 25853 |
rs772076053 | snp | C/T | 3.34146e-05 | 0.00408732 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107563 | GACATCTACGACAAA[C/T]AGCTACAAGAAAAAA | 25853 |
rs772165864 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125029 | GGCACTTACCGTGTT[A/G]CATTTTGTGCCACAC | 25853 |
rs772167922 | snp | A/G | 1.73258e-05 | 0.00294323 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089598 | CCGGATTCCTGAAAG[A/G]CAGAAAAGTAAAAGG | 25853 |
rs772186510 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090520 | CAGTGCTTGGGATAT[A/G]AAGATGTCTCTTGGC | 25853 |
rs772225634 | snp | A/T | 2.30258e-05 | 0.00339299 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126465 | GGCCCCGCAGCCACA[A/T]GGGGCGGGGGAAGCG | 25853 |
rs772257003 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117562 | TCACCACATAAACTT[C/T]GACAACATACAACAG | 25853 |
rs772268548 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096054 | GCCTTTGGAGAACTG[A/G]TCTTTTAAACAAGAA | 25853 |
rs772318033 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098160 | GGGTGGGTTTCAGAG[C/T]CTCAGTTATAATTTC | 25853 |
rs772329409 | snp | A/C | 1.64795e-05 | 0.00287045 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093273 | GGCCTGAGGTGCACA[A/C]AGGGACTCTTACCAC | 25853 |
rs772351265 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104682 | GCATTTTAGGAGGCC[A/G]AGGCAGGTGGATCAA | 25853 |
rs772478894 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | DCAF12 | GRCh38.p7 | 9:34088504 | CTCCAGGTTTCATCA[C/T]GATTCTACGGGAAGA | 25853 |
rs772545356 | snp | C/T | 1.7339e-05 | 0.00294435 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098548 | AACACAGATGTCAGA[C/T]GTACCCACCCCTCTA | 25853 |
rs772565547 | snp | A/T | 1.74369e-05 | 0.00295265 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088374 | GAGCCCAGCATAGTT[A/T]CCATGGAGCCCTGAA | 25853 |
rs772613838 | snp | A/G | 1.71334e-05 | 0.00292684 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098287 | CAAGACATAAGCAAG[A/G]GGAATACACGTCAGG | 25853 |
rs772633369 | in-del | -/TGCTATTTCTGGGTATCTGCACGAG | 1.71132e-05 | 0.00292511 | splice-acceptor-variant | DCAF12 | GRCh38.p7 | 9:34089592 | ACTGACCGGATTCCT[-/TGCTATTTCTGGGTATCTGCACGAG]GAAAGACAGAAAAGT | 25853 |
rs772642118 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122637 | ACCCACCATCATGCC[C/T]AGCTAATTTGTTTGT | 25853 |
rs772739633 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095490 | AGCTCAAGTGGTCCT[C/T]CTGCCTCAGCACTGC | 25853 |
rs772776180 | snp | A/G | 9.94316e-05 | 0.00705024 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34096746 | TTCAGCCTTCCAGAG[A/G]TGAAAGTAGCCATCC | 25853 |
rs772841289 | snp | C/G | 3.68766e-05 | 0.00429382 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126356 | TCTCAACCCTCACCT[C/G]CGGGCCCTGAGCGTC | 25853 |
rs772967025 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108874 | TGTAGTCCCAACTAC[G/T]TAGCTACTCAGGAGG | 25853 |
rs773060859 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125035 | TACCGTGTTGCATTT[C/T]GTGCCACACACCACT | 25853 |
rs773063310 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103760 | CTTGAGGGGATCTCT[C/T]AATCCTGGGAGTTCG | 25853 |
rs773079876 | snp | A/G | 3.39916e-05 | 0.00412246 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107574 | CAAATAGCTACAAGA[A/G]AAAATGGATACAGAA | 25853 |
rs773121323 | snp | G/T | | | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34096755 | CCAGAGATGAAAGTA[G/T]CCATCCAGAGACACT | 25853 |
rs773128146 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122601 | CCTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATTA | 25853 |
rs773165467 | snp | C/T | 0.000467991 | 0.0152897 | intron-variant | DCAF12 | GRCh38.p7 | 9:34106411 | TGCCACATCAAAAGC[C/T]CCCTATAAAAGGGCA | 25853 |
rs773292443 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104697 | GAGGCAGGTGGATCA[A/G]CTGAGGTCCTGCATT | 25853 |
rs773311518 | snp | A/G | 2.33987e-05 | 0.00342035 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126468 | CCCGCAGCCACATGG[A/G]GCGGGGGAAGCGAAG | 25853 |
rs773323087 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091120 | TCACTTGAGGTCAGG[A/C]GTTCAAAACCAGTCT | 25853 |
rs773345366 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090843 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCACCA | 25853 |
rs773416177 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093275 | CCTGAGGTGCACACA[A/G]GGACTCTTACCACTG | 25853 |
rs773438636 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115745 | TTGAACTACTGTACA[A/T]CTTTTTTAATTATAG | 25853 |
rs773462144 | snp | A/G | 5.11208e-05 | 0.00505547 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34088389 | TCCATGGAGCCCTGA[A/G]GGGAGGGGACCTCCT | 25853 |
rs773506749 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119136 | ACTCACTGTGTGACT[-/A]AGAGGAGCAACTCCT | 25853 |
rs773738124 | in-del | -/GAG | 8.26262e-05 | 0.006427 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093458 | GAGGAGCTGAAAATA[-/GAG]GAGAGATATAACCAT | 25853 |
rs773741482 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099973 | TGGGCAGTAGGGCTT[A/G]GGAATCCTCCCCTCT | 25853 |
rs773756188 | snp | A/C | 1.67475e-05 | 0.00289369 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125305 | CATTAGAAATCAGGG[A/C]TTTGGCTACTCTTCT | 25853 |
rs773797140 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103279 | CGGCGTGGTGGCACG[C/T]GCCTGTAGTCCCAGC | 25853 |
rs773804272 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118855 | TGTAATCCCAGCTAC[C/T]TGGTGGTGCTGAAGC | 25853 |
rs773863593 | snp | C/G | 1.6599e-05 | 0.00288084 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093472 | AGAGGAGAGATATAA[C/G]CATGGCATCAGCAGA | 25853 |
rs773908031 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125179 | AGAGTAGCTGGTTTC[A/G]TTCTGTAGCCTGACT | 25853 |
rs773965832 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117709 | CACCTGAGGTTGGGA[C/T]TTCGAGACCAGCCTC | 25853 |
rs774019176 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34122972 | TAAACCATGAACATA[C/T]ACCTAACCCATCCCA | 25853 |
rs774034512 | snp | G/T | 1.66305e-05 | 0.00288357 | missense | DCAF12 | GRCh38.p7 | 9:34096720 | GTTCATCACACCTTA[G/T]ATAGTGTATTTTCAG | 25853 |
rs774062303 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101795 | TGAGGTAGGTGGACC[A/G]CCTGAGCTCAAGAGT | 25853 |
rs774084701 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112507 | GCTGAGGCAGGAGAA[-/T]TGCTTGGACCCAGGA | 25853 |
rs774303586 | snp | A/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127680 | GCCTTCGCTTTCCTC[A/T]AGCAAACAAACCCTC | 25853 |
rs774384995 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095271 | GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGC | 25853 |
rs774492624 | snp | A/G | 1.72576e-05 | 0.00293743 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089595 | TGACCGGATTCCTGA[A/G]AGACAGAAAAGTAAA | 25853 |
rs774504571 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093709 | TAATCAGAAGTAGCT[A/G]GAAAGGCCAAGGCCT | 25853 |
rs774517270 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104651 | CCAGGTGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 25853 |
rs774555698 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095778 | TGATTATTTCAGAGA[C/T]GGTTTATCTTAATTT | 25853 |
rs774559250 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107523 | GGTCTTTCAGAATGG[A/G]GATCTTGGTGATCTG | 25853 |
rs774576896 | snp | C/G/T | 4.51113e-05 | 0.00474911 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126457 | GCCGCCGCGGCCCCG[C/G/T]AGCCACATGGGGCGG | 25853 |
rs774591187 | snp | C/G | 1.64743e-05 | 0.00287 | missense | DCAF12 | GRCh38.p7 | 9:34098431 | TGTGTGCATACACAG[C/G]GACCCGTGACACATT | 25853 |
rs774686751 | snp | A/G | 1.8627e-05 | 0.00305175 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126385 | TCGCTCCCAGCTCCC[A/G]GCGAGGCGGGCGCTT | 25853 |
rs774708905 | in-del | -/TAGCAGTGGGTGTAAACAGCAT | 1.64906e-05 | 0.00287142 | frameshift-variant | DCAF12 | GRCh38.p7 | 9:34088434 | GTTCCAGACGAGTCG[-/TAGCAGTGGGTGTAAACAGCAT]TAGCAGTGGGTGTAA | 25853 |
rs774778226 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090743 | CACTGCAACCTCCAC[A/C]TCCCAGATTCAAGTG | 25853 |
rs774863794 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111373 | CTCTAAATGTCCAGG[A/C]TGATCAAGTGCCTCT | 25853 |
rs774873428 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117665 | CACACCTGTAATCCC[A/T]GCACTTTGGGAGGCC | 25853 |
rs774880932 | snp | A/G | 1.69588e-05 | 0.00291189 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098522 | ATCACGTGAGCCTGC[A/G]GGGCCAGGAGAACAC | 25853 |
rs774897042 | in-del | -/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109007 | ATATATATATATGGT[-/T]TTTTTTTTTTTCACT | 25853 |
rs775007000 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125069 | CTATGATTCAACCAC[C/T]GAGATGCAAACACTT | 25853 |
rs775115214 | snp | G/T | 0.000500322 | 0.0158086 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088346 | TGCATTTGGGGAGTT[G/T]TCATTAACTCCAGAG | 25853 |
rs775160589 | snp | C/T | 4.94181e-05 | 0.00497057 | missense | DCAF12 | GRCh38.p7 | 9:34093319 | AACAGACAGACTTGA[C/T]GTTGTATGATGGCTG | 25853 |
rs775164771 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125170 | CAACACTCGAGAGTA[A/G]CTGGTTTCATTCTGT | 25853 |
rs775264703 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34098453 | TGACACATTGTGTCT[C/T]GCATCACTTTTGGTC | 25853 |
rs775390194 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093914 | CGCTATAGAAAGCAC[A/G]CCCATGGGACTAGCT | 25853 |
rs775398262 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118674 | ATAGTGTTAAATAAT[A/G]ATAATATGGCCGGGC | 25853 |
rs775412873 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34124813 | GGGCCTGAAGAAATA[C/G]ACTCCTTTGAGGACT | 25853 |
rs775496390 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113673 | CAATACAAAACACTA[C/T]AAAACAAAAACAATT | 25853 |
rs775540224 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126185 | GCCCTGGCCTATCTG[C/T]CCTCCAGTTAACGAG | 25853 |
rs775650096 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107383 | ACACACAGGATCCAG[C/T]GTAGGTAGTCGATAG | 25853 |
rs775657557 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112625 | AAATATTGGCTGGGT[C/G]TGGTGGCTCACACCT | 25853 |
rs775737837 | snp | C/T | 1.64814e-05 | 0.00287061 | missense | DCAF12 | GRCh38.p7 | 9:34089473 | CTGGGCTTGGACCCA[C/T]AACAAGCTGAGAGCC | 25853 |
rs775842533 | in-del | -/TTTTTTTTTT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095373 | CCACCGCGCCAGGCC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 25853 |
rs775904193 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089331 | GTATGAGTAGATGGT[C/G]TGTCAGTGGGGGCTG | 25853 |
rs775926966 | snp | A/C | 1.68564e-05 | 0.00290309 | intron-variant | DCAF12 | GRCh38.p7 | 9:34125319 | GCTTTGGCTACTCTT[A/C]TTCAGAACAGATCCT | 25853 |
rs775989449 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096170 | AAACCAGCCTGGGAA[A/T]CATAGTGAGACTCTG | 25853 |
rs776023183 | snp | G/T | 1.82607e-05 | 0.00302159 | missense, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126367 | ACCTGCGGGCCCTGA[G/T]CGTCGCTCCCAGCTC | 25853 |
rs776109707 | snp | C/T | 2.21511e-05 | 0.00332792 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126449 | TGGGCAGCGCCGCCG[C/T]GGCCCCGCAGCCACA | 25853 |
rs776168963 | snp | A/G | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127939 | CCTAATGTCTTGCGA[A/G]AGGCAGCTCCATCTT | 25853 |
rs776176441 | snp | C/T | 1.71173e-05 | 0.00292547 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098294 | TAAGCAAGAGGAATA[C/T]ACGTCAGGGATCCCT | 25853 |
rs776264815 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | DCAF12 | GRCh38.p7 | 9:34098404 | GGATGTCCTTTAAGG[C/T]CTTGTGAGTGATGTG | 25853 |
rs776387996 | snp | A/G | 1.65146e-05 | 0.0028735 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093451 | TGGTGGAGAGGAGCT[A/G]AAAATAGAGGAGAGA | 25853 |
rs776435998 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117460 | CGGCCTCTAATCCTT[C/G]ATTTTGGAGGTCTCT | 25853 |
rs776501968 | snp | C/T | 3.29495e-05 | 0.00405877 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093283 | GCACACAGGGACTCT[C/T]ACCACTGCCTCGCTC | 25853 |
rs776519265 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104850 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 25853 |
rs776530184 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115607 | CGTCTCAAAAAAAAA[A/G]AAGTATATATATACA | 25853 |
rs776569664 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111608 | AACTACTGTAGTAGG[C/G]CCCCACATCCCTGTG | 25853 |
rs776574224 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090985 | TTCTCTACTACTCTC[A/G]TTATACATTATTCTT | 25853 |
rs776574368 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105731 | CTTCCTTTTTTATCT[A/G]TCTATCTTATCTATC | 25853 |
rs776710696 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125778 | CAGTTGCAGAATTCG[-/A]AAAAATCAACCGCCA | 25853 |
rs776716182 | snp | C/T | 1.77404e-05 | 0.00297824 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098564 | GTACCCACCCCTCTA[C/T]GGGAAATCCCACAGA | 25853 |
rs776981175 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092537 | CTAAAAATACAAAAA[G/T]TAGCTGGGCGTGGTG | 25853 |
rs776981961 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | DCAF12 | GRCh38.p7 | 9:34089462 | CCCCTGCTAGTCTGG[A/G]CTTGGACCCATAACA | 25853 |
rs777094381 | in-del | -/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111195 | TCACCATATTGGCCA[-/G]GGCTGGTCTGGAACT | 25853 |
rs777097370 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121841 | CCAGCTACTCAGGAG[C/G]CTGAGGCGGGAGAAT | 25853 |
rs777192076 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34100103 | ATAGTGGCACAATCA[C/T]AGCTCACTGCAGGCT | 25853 |
rs777208605 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34098770 | TTGAAATTTATTTAT[C/T]ATTATTATTTTTTTT | 25853 |
rs777231396 | snp | A/G | 9.89707e-05 | 0.00703389 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093240 | TGAAAGTCAGAACCC[A/G]TATGCAGTGCAGCTG | 25853 |
rs777235990 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34104165 | AGCTACTTGGGAGGC[C/T]GAGGCAAGAGAAGTG | 25853 |
rs777266832 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112636 | GGGTGTGGTGGCTCA[C/G]ACCTGTAATCCCAGT | 25853 |
rs777358954 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090254 | TTTTCAGGAGAGACA[C/G]GGTTTCACCATGTTG | 25853 |
rs777404162 | snp | A/G | 1.6489e-05 | 0.00287128 | missense | DCAF12 | GRCh38.p7 | 9:34098466 | CTCGCATCACTTTTG[A/G]TCAAAACATCATCTG | 25853 |
rs777422806 | in-del | -/C | | | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34086906 | TATGACTTTTCCTTT[-/C]CCCAAAATGGGATGT | 25853 |
rs777431326 | snp | G/T | 4.19103e-05 | 0.00457749 | utr-variant-5-prime, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126436 | TTCCGGGCCATAGTG[G/T]GCAGCGCCGCCGCGG | 25853 |
rs777446615 | snp | A/G | 1.64743e-05 | 0.00287 | missense | DCAF12 | GRCh38.p7 | 9:34098389 | TTGTGTCTTCTTTGG[A/G]GATGTCCTTTAAGGC | 25853 |
rs777609684 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111797 | AAACCGCCCGGGTGG[C/T]CACTTTTTACCAAAG | 25853 |
rs777615835 | in-del | -/GACATCTAC | 1.65416e-05 | 0.00287586 | cds-indel | DCAF12 | GRCh38.p7 | 9:34107548 | GATCTGGCTTGTCTG[-/GACATCTAC]GACAAATAGCTACAA | 25853 |
rs777893053 | snp | C/G/T | 0.000115312 | 0.00759245 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125151 | GCTGTGCTGCATAAC[C/G/T]ATGCAACACTCGAGA | 25853 |
rs778009239 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | DCAF12 | GRCh38.p7 | 9:34093414 | TAAGCCAGACACACA[C/T]TCTCACGGCAATATG | 25853 |
rs778096184 | snp | G/T | 1.68434e-05 | 0.00290197 | intron-variant | DCAF12 | GRCh38.p7 | 9:34093497 | AGCAGAGAGGGTAAG[G/T]CAGGGATATTGTTTC | 25853 |
rs778180106 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105527 | GGTGTGTGCCTATAG[C/T]CCCAGCTACCTGGGA | 25853 |
rs778215349 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | DCAF12 | GRCh38.p7 | 9:34107329 | TTAAAAACAAGGCTC[C/T]CTCCAACTACAACTA | 25853 |
rs778232487 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34113177 | TGCCTCAGCCTCGCC[A/G]AGTACCTGGGATTAC | 25853 |
rs778268796 | snp | C/T | 3.30044e-05 | 0.00406216 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089448 | TAGTTTCAGATTCTC[C/T]CCTGCTAGTCTGGGC | 25853 |
rs778368662 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107453 | AGTGTTCTAGAAGGA[C/T]TCAGCTCGATGGCAT | 25853 |
rs778395986 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34125339 | GAACAGATCCTACTG[C/T]ATTACAGAAATCACC | 25853 |
rs778412324 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34094814 | GGATTATAGGCGTGA[A/G]CCACCGCACCCGGCC | 25853 |
rs778425286 | in-del | -/TCACA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103043 | TGCAGTGAGCCATGA[-/TCACA]TCACGCCACTGCATT | 25853 |
rs778555779 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon | DCAF12 | GRCh38.p7 | 9:34089520 | CTGAGCTCGGATGTC[A/G]TAGAACAGCAGGGAG | 25853 |
rs778557229 | snp | C/T | 1.95904e-05 | 0.00312966 | synonymous-codon, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126420 | CTTCCTGCTAACTAC[C/T]TTCCGGGCCATAGTG | 25853 |
rs778579395 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | DCAF12 | GRCh38.p7 | 9:34098361 | AGAGCCCGAACCTTG[C/T]AGTTGTCAGGGTTTG | 25853 |
rs778593710 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096617 | TCAAAAATAAATGAA[C/T]AGATAAAATAAACAT | 25853 |
rs778665963 | snp | G/T | 1.64904e-05 | 0.00287139 | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34126333 | GCCTCACCACCCAGG[G/T]GCCGGCCTCTCAACC | 25853 |
rs778701915 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34110914 | ATGAAAAATTCTTCA[A/G]TGAAATATAATTATT | 25853 |
rs778757764 | snp | A/G | 1.71708e-05 | 0.00293003 | | | GRCh38.p7 | 9:34098275 | GAGTGCATATCCCAA[A/G]ACATAAGCAAGAGGA | 25853 |
rs778861103 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109844 | GTCGGAAGCAGATGT[C/T]TTAGAGAGCTTCCTT | 25853 |
rs778892268 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34117046 | CACTCTGAGCTGTGA[A/C]TCTAAACTGTTCCTA | 25853 |
rs778936781 | snp | C/G/T | 3.60576e-05 | 0.00424591 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088305 | AAGAAACAAGGAAAC[C/G/T]GAGAATGGAAGTTAG | 25853 |
rs778997713 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112796 | CTAGCTACTCGGGAG[A/G]CTGAGGCAGGTGAAT | 25853 |
rs779102123 | in-del | -/CT | 0.000121234 | 0.00778475 | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127284 | AGGCTCCATTCTCCG[-/CT]CTGTCTCCTCCTGAT | 25853 |
rs779214729 | in-del | -/TT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109006 | TATATATATATATGG[-/TT]TTTTTTTTTTTCACT | 25853 |
rs779228057 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105485 | ATTTTAAAATGTCAA[C/T]AGTCGTTATTACTAG | 25853 |
rs779236513 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125134 | CAGGAGACTGGGAAG[C/T]TGCTGTGCTGCATAA | 25853 |
rs779247270 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116229 | GGGCATGGTGGCAGT[C/T]GCCTTTAATCCCAGT | 25853 |
rs779400337 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | DCAF12 | GRCh38.p7 | 9:34093375 | GCTTGGGAGCCCACT[A/G]CATAAACTGACCATT | 25853 |
rs779416665 | snp | C/G | 2.07803e-05 | 0.00322331 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34106450 | AGACACTGCCATAGT[C/G]TCGCTGATCCATGCG | 25853 |
rs779450950 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34105408 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACCCTGTG | 25853 |
rs779468372 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090551 | CATAAGAACTGGATA[-/AT]ATATTTGTGGAACCA | 25853 |
rs779607013 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34107508 | CACCTCCAGGCTCCC[A/G]GTCTTTCAGAATGGG | 25853 |
rs779730660 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34101715 | TTCTATTAAGAATGA[C/G]TGTTCTAGACCGTTC | 25853 |
rs779806422 | snp | C/G | 5.02803e-05 | 0.00501374 | intron-variant | DCAF12 | GRCh38.p7 | 9:34089408 | CAGGTAGGGGCTTAC[C/G]CACCAGCCAGCCTTT | 25853 |
rs779830425 | snp | A/G | 0.00012351 | 0.00785747 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125663 | TCTGTACTCCCACTG[A/G]AGCACGGAAGATACA | 25853 |
rs779890365 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34099420 | TATTTTTAGTAGAGA[A/T]TGGGTTTCACCATAT | 25853 |
rs779918234 | snp | A/G | 1.67835e-05 | 0.0028968 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096819 | GTTATATTATCATCT[A/G]TAGCAACTAATGTAC | 25853 |
rs780048121 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116854 | GGCACAGTGACGGGT[A/G]TGTAATCCCAGCTAC | 25853 |
rs780085531 | snp | G/T | 3.35065e-05 | 0.00409293 | intron-variant | DCAF12 | GRCh38.p7 | 9:34098318 | GATCCCTACACAAGT[G/T]CATACCTTGTTCTTG | 25853 |
rs780130855 | snp | G/T | | | upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34127497 | CACTCTTGGATTCAG[G/T]TTGCGTCTCCATTAG | 25853 |
rs780146144 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34092897 | ATTGCCCAGGCTGGA[A/G]TGCAATGGTGCGATC | 25853 |
rs780184057 | in-del | -/A | 0.000123419 | 0.00785456 | intron-variant, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125658 | TCAGTCTGTACTCCC[-/A]ACTGGAGCACGGAAG | 25853 |
rs780257390 | snp | C/T | 1.66117e-05 | 0.00288194 | missense | DCAF12 | GRCh38.p7 | 9:34089567 | CAGTGATGATGTGCT[C/T]GTAGAAACTCACTGA | 25853 |
rs780386449 | snp | A/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34096482 | GGCAGACGCCTGTAA[A/T]CCCCGCAGCTACTCA | 25853 |
rs780415826 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34090548 | GGCACATAAGAACTG[G/T]ATAATATTTGTGGAA | 25853 |
rs780416438 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34116214 | ATATAAAAATTAGCC[A/G]GGCATGGTGGCAGTC | 25853 |
rs780445611 | snp | A/G | 1.66905e-05 | 0.00288876 | intron-variant | DCAF12 | GRCh38.p7 | 9:34124996 | TCCACGACCTAGGAG[A/G]GAGGTCACATCCCCC | 25853 |
rs780850203 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34118507 | GAAAATCTGTACACA[A/G]GAAACTTTCAGGTTT | 25853 |
rs780851432 | snp | C/T | 1.65726e-05 | 0.00287855 | stop-gained | DCAF12 | GRCh38.p7 | 9:34098489 | ATCATCTGTCACCTC[C/T]CAGAGTCCCATAGAA | 25853 |
rs780866460 | snp | C/G | 6.58968e-05 | 0.00573969 | missense, utr-variant-5-prime | DCAF12 | GRCh38.p7 | 9:34125163 | AACCATGCAACACTC[C/G]AGAGTAGCTGGTTTC | 25853 |
rs780939428 | snp | C/T | 5.38102e-05 | 0.00518673 | utr-variant-3-prime | DCAF12 | GRCh38.p7 | 9:34088336 | TGTAAATCTCTGCAT[C/T]TGGGGAGTTGTCATT | 25853 |
rs780941540 | snp | A/C | 0.000244496 | 0.0110539 | splice-donor-variant | DCAF12 | GRCh38.p7 | 9:34106432 | TAAAAGGGCAACTTT[A/C]CCAGACACTGCCATA | 25853 |
rs780972550 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34095361 | TATAGGCGTGAACCA[A/C]CGCGCCAGGCCTTTT | 25853 |
rs780985040 | in-del | -/AA/AAA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34091639 | GAGGACCCTGTCTTC[-/AA/AAA]AAAAAAAAAAAAAAA | 25853 |
rs781037659 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34123952 | CAACAGAAGAGGAAA[C/T]GAAAGGTTGGCCCCA | 25853 |
rs781081801 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119228 | TTAGGATAAGAAAAC[A/G]CAAGGTTCATCTAGC | 25853 |
rs781102885 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | DCAF12 | GRCh38.p7 | 9:34088442 | ACGAGTCGTAGCAGT[A/G]GGTGTAAACAGCATT | 25853 |
rs781218779 | snp | A/C | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34097348 | CTCACTGCCAACCTC[A/C]ACCTCCTATAGTTTT | 25853 |
rs781260468 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF12 | GRCh38.p7 | 9:34125982 | TTCCAGGAGGGACGC[A/C]ATCATCCCAGCTTCC | 25853 |
rs781307744 | snp | A/T | 3.37058e-05 | 0.00410509 | intron-variant | DCAF12 | GRCh38.p7 | 9:34096695 | TTATTAGGTAAAACC[A/T]CAAAATCATGTTCAT | 25853 |
rs781460964 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34119386 | AGGTTCCTGTTTAGT[C/T]TTCAACCACATATAT | 25853 |
rs781554437 | snp | G/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34106526 | TAACAGGTACAGGGA[G/T]GAAAATAAGAAATTA | 25853 |
rs781609586 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34093782 | TCGTTCCAGGGCACT[A/G]AAGCCATAGTCCCAC | 25853 |
rs781609593 | snp | C/T | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34107857 | CCTTCTATTAGGCCA[C/T]GGACACAAAGAGGAA | 25853 |
rs781625013 | snp | C/T | 1.6528e-05 | 0.00287467 | missense | DCAF12 | GRCh38.p7 | 9:34089552 | CCTGCCCTGTTCCCA[C/T]AGTGATGATGTGCTC | 25853 |
rs781698832 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34114818 | ATGGCTTAAAAAAAA[C/G]GAGTCAGATGTGGTA | 25853 |
rs781768494 | snp | C/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34121874 | ATTGAACCCAGGAGG[C/G]AGAGGTTGCAGTGAG | 25853 |
rs796076842 | in-del | AA/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34115437 | CTACTAAAAATACAA[AA/G]AATTAGCCGGGCGGC | 25853 |
rs796310602 | in-del | -/AA | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34108811 | AAAAAATAAATAAAT[-/AA]ATATATATATATATA | 25853 |
rs796411748 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34111981 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAATTA | 25853 |
rs796427002 | in-del | -/ATCAC | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34103047 | GTGAGCCATGATCAC[-/ATCAC]GCCACTGCATTCCAT | 25853 |
rs796608502 | snp | A/G | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34089849 | CAGATTCCCGATGAT[A/G]CTCAAGATGCTTTTG | 25853 |
rs796874253 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34120670 | GCAAGACGCGGTCTC[-/A]AAAAAAAAAAAAAAA | 25853 |
rs796896248 | in-del | -/AT | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34109002 | TATATATATATATAT[-/AT]GGTTTTTTTTTTTTT | 25853 |
rs796938308 | snp | A/G | | | downstream-variant-500B | DCAF12 | GRCh38.p7 | 9:34086123 | TACTTATGTAACAGA[A/G]GTAACGTCACACTAC | 25853 |
rs796997762 | in-del | -/A | | | intron-variant | DCAF12 | GRCh38.p7 | 9:34112142 | GTGAGACTCCAACTC[-/A]AAAAAAAAAAAAAAG | 25853 |