SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1954 | snp | A/G | 0.000378928 | 0.0137594 | missense | DCAF13 | GRCh38.p7 | 8:103441608 | CATACTTTCGTCGAC[A/G]AGCTTCTTTCATGAT | 25879 |
rs750509 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416628 | AGAATCACAGAAGAC[A/G]GGTGCTGAAGGGGGC | 25879 |
rs750605 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416181 | TGAACCTAAGGCATA[A/G]AAAGAAGGGCTGTGT | 25879 |
rs750606 | snp | C/T | 0.316726 | 0.240931 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416302 | TGTGAGCATTGCTAA[C/T]AAGTCTCTGCTCAAA | 25879 |
rs751725 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436854 | TTTTCTCAAAAAATT[A/G]TGATAATTGGATGAT | 25879 |
rs893044 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436870 | TGATAATTGGATGAT[C/T]ATGGTCATAGTCAAT | 25879 |
rs975440 | snp | A/G | 0.376989 | 0.215346 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435425 | GGAAAATGTGTTGGT[A/G]TATATATAAGTGGAG | 25879 |
rs1370005 | snp | A/C | 0.362014 | 0.223501 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432781 | ACAATTAAGCCATTC[A/C]TGATAGAAATACACA | 25879 |
rs1370006 | snp | C/T | 0.378174 | 0.214642 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426335 | CAAAAAAAAAAAAAA[C/T]TGTTAAAATTCTTTA | 25879 |
rs1436595 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433132 | CTGTAAAGGGCCAAA[C/T]GTTAAACATTTTCAG | 25879 |
rs2304501 | snp | C/T | 0.376989 | 0.215346 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431055 | AGTGTACATGTCATA[C/T]GATAATCATGGGGCT | 25879 |
rs2304502 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442718 | TCAGAAAAATCAAAG[C/T]ATTTTCTTTCACTAG | 25879 |
rs2892544 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417051 | ACATTATCATTTTGG[A/G]TATGCTTTCTTTGTG | 25879 |
rs3098214 | snp | G/T | 0.489722 | 0.0709447 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442566 | TAAGTTTAAAAACCT[G/T]CCACAGTTAATAAAA | 25879 |
rs3098215 | snp | C/T | 0.376791 | 0.215463 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441375 | AGAAAGCACCCTTTT[C/T]CCCCTAACCTAATCT | 25879 |
rs3098216 | snp | C/T | 0.00129525 | 0.0254155 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440125 | CCTCCCTATAGAAAA[C/T]GAATTAAGTTAAAAC | 25879 |
rs3098217 | snp | C/T | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440053 | TAAGTATCAGGATAC[C/T]ATTTCTGAGTCCTAT | 25879 |
rs3098218 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439971 | CAACTAATAAGGTTC[C/T]GTGTTAAGTGCTGGG | 25879 |
rs3098219 | snp | A/G | 0.48978 | 0.0707512 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439813 | ATATGATGTTCAACC[A/G]AGGTAACTTTGTAAC | 25879 |
rs3098220 | snp | A/T | 0.371582 | 0.218444 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439306 | CTGATAAGTTGAGGT[A/T]AGAATAATTTAATAG | 25879 |
rs3098221 | snp | C/G | 0.489893 | 0.0703642 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438254 | GCTTTTTCTTCTCCC[C/G]CTCAGTGCTCTGCTT | 25879 |
rs3098222 | snp | C/T | 0.499187 | 0.0201513 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435961 | AAGCAACAGGCCATA[C/T]CATATGACCACACAG | 25879 |
rs3098223 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434877 | atgtaagagtgAACA[C/T]GGCCTTTCAAAGGGT | 25879 |
rs3098224 | snp | A/G | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434468 | TCCTGCCTAAGAACA[A/G]TGGTTTTCAGCTAGG | 25879 |
rs3098225 | snp | C/T | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434448 | TTTCAGCTAGGTTTG[C/T]TTGGTTCCAGCAAAC | 25879 |
rs3098226 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428834 | ATCCCTAATAATTAC[A/G]ATTTTAGAATTGGTG | 25879 |
rs3098227 | snp | A/G | 0.370974 | 0.218781 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428523 | GAGAAAGATATAATA[A/G]AGACAGACACTCCAG | 25879 |
rs3098234 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423677 | ACTTATTATTTTGTG[G/T]TGAGAACATTTAATT | 25879 |
rs3098235 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422974 | CCGAATCTTTTAACA[C/G]TAACACCTATTTCCA | 25879 |
rs3098236 | snp | G/T | 0.378765 | 0.214288 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422794 | CCTACATTTTATAAC[G/T]CAGCTCAACCTGTTT | 25879 |
rs3098237 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422120 | TCAATCCTCCAAAGT[A/G]TCAACCACTGATTTC | 25879 |
rs3098238 | snp | A/G | 0.0941315 | 0.195461 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420403 | ATGCTTTGCCAAGCA[A/G]TTGACTCCATCACGG | 25879 |
rs3098239 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419175 | CGCTTAGggccgggc[A/G]tggtggctcacgcct | 25879 |
rs3098240 | snp | A/G | 0.489722 | 0.0709447 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417596 | GGAGTGCAGTGACGC[A/G]ATCTCGGCTCACTGC | 25879 |
rs3098241 | snp | C/T | 0.331411 | 0.236373 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413076 | TGACAGATAAAAGGA[C/T]TGAGTTTGGATTGGA | 25879 |
rs3133817 | snp | A/G | 0.372995 | 0.217652 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414017 | CCCATACAGCAGTCT[A/G]CAAATATTAAGAGAA | 25879 |
rs3133818 | snp | A/C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419127 | ctgacctcgtgatcc[A/C/G]tccgtcccggccccc | 25879 |
rs3133819 | snp | C/T | 0.345037 | 0.231231 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419177 | GCGTGAGCCACCACG[C/T]CCGGCCCTAAGCGTG | 25879 |
rs3134249 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416634 | TTCAGCACCTGTCTT[A/C]TGTGATTCTATCACT | 25879 |
rs3134250 | snp | A/G | 0.373196 | 0.217538 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417997 | gccgggcatggtggc[A/G]ggtgcctgtagtccc | 25879 |
rs3134251 | snp | A/G | 0.378174 | 0.214642 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418970 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 25879 |
rs3134252 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419517 | CATAATCACAACTTC[A/G]TGTGTCTATCAGCAC | 25879 |
rs3134253 | snp | A/G | 0.359518 | 0.224735 | missense | DCAF13 | GRCh38.p7 | 8:103420317 | GTCCCACGAGAATAT[A/G]TAAGAGCTTTAAATG | 25879 |
rs3134257 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423309 | ACCTAAAGTGTCCAG[A/C]AATGGATGAATGAAT | 25879 |
rs3134258 | snp | G/T | 0.373397 | 0.217424 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423506 | ccaaactcttagaaa[G/T]ggagtaaaatggtca | 25879 |
rs3134260 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424650 | GCAGAACAGCTTGGT[C/T]ATTTACAAGCAAATT | 25879 |
rs3134261 | snp | C/T | 0.378174 | 0.214642 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426425 | CCCATGGGAAGACCA[C/T]GGAGAAAAAGATAGA | 25879 |
rs3134263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428048 | TTAGGTAGTATGAGA[A/G]AAAAATCCTAATATG | 25879 |
rs3134264 | snp | C/T | 0.489608 | 0.0713316 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428815 | CTGTGTCAGAAGAGC[C/T]GATCACCAATTCTAA | 25879 |
rs3134265 | snp | A/G | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429695 | GAGAGTTAACAACAC[A/G]AAGAAACATTTACTA | 25879 |
rs3134267 | snp | C/T | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434641 | GAAACTATGTAGATA[C/T]CCTCTTCTCAGACTT | 25879 |
rs3134268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437533 | ATATTTCATTTCTAA[G/T]AAATTGTCTCCTGAT | 25879 |
rs3134270 | snp | C/G | 0.379158 | 0.214052 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439213 | GTTTCACCTGGTCTC[C/G]ATCTCCTGACCTCGT | 25879 |
rs3134271 | snp | C/T | 0.371177 | 0.218669 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439309 | TTAAATTATTCTTAC[C/T]TCAACTTATCAGACA | 25879 |
rs3134272 | snp | C/G | 0.49917 | 0.0203505 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441913 | TAGGACTACAGGCAC[C/G]CGCCACCATGCGCGG | 25879 |
rs3134273 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442084 | GGCCATTTCTTTTTC[C/T]TTTTCCCAAAAAAGG | 25879 |
rs3134274 | snp | C/T | 0.0198 | 0.0975088 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443164 | TACTTTCTCTTTGAT[C/T]TATTATTGTAGACAC | 25879 |
rs3134291 | snp | C/T | 0.489722 | 0.0709447 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413381 | CTTATAGAGGTAATA[C/T]GGTGAGGGGTTAAGT | 25879 |
rs3134292 | snp | A/C | 0.372995 | 0.217652 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413817 | CAATCTTCCACTGAA[A/C]CTTAAAGATACACAT | 25879 |
rs3134293 | snp | C/T | 0.316968 | 0.240864 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413856 | GTAATGTAGAATTTT[C/T]TTAACGGTTTACCTG | 25879 |
rs3134294 | snp | A/C | 0.0460142 | 0.144533 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414570 | CTCAGACTTCTCTAC[A/C]TACATGCCCCCTCTC | 25879 |
rs3134295 | snp | A/C | 0.49294 | 0.0589944 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415131 | AAGAACGGGGCACAG[A/C]CACTACGTCACGCCG | 25879 |
rs3134296 | snp | C/T | 0.301032 | 0.244736 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415313 | AGGATCCAGTTGAGC[C/T]AGCAGGCCGCCGCTC | 25879 |
rs3134297 | snp | C/T | 0.360292 | 0.224356 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415350 | TCACGTGACTGGAAG[C/T]AGTCTGGGAAAAGCG | 25879 |
rs3814106 | snp | A/C/G | 0.000102697 | 0.00716517 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415006 | GCGACCGTCGCCACG[A/C/G]TGGCGGCCACTGCAT | 25879 |
rs3837183 | in-del | -/ACAAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426042 | CATCATCATAATAAA[-/ACAAA]TATTTCTAGGTTGGT | 25879 |
rs4634606 | snp | A/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418868 | tatatatatatatat[A/T]tTTtttttttttttt | 25879 |
rs5025988 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414678 | CCAACGCGGACAGCA[A/C]CSCTCCCTTCAACGC | 25879 |
rs5893653 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414680 | CAACGCGGACAGCAC[C/G]CCCCTTCAACGCTCC | 25879 |
rs5893654 | in-del | -/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414682 | ACGCGGACAGCACCC[-/T]CCCTTCAACGCTCCT | 25879 |
rs5893655 | in-del | -/A | 0.372391 | 0.217992 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417343 | TTTCTTAAAAAAAAA[-/A]GATCTTTGGCTGGGC | 25879 |
rs7813024 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418866 | tatatatatatatat[A/T]tTTTTtttttttttt | 25879 |
rs7815341 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430052 | gtaggtaagtaaaat[A/G]tgTTTTATTACAAAT | 25879 |
rs7816297 | snp | A/G | 0.376592 | 0.215579 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430438 | CATGAGGATTTTACA[A/G]TGAAAATACTTGGTT | 25879 |
rs7820295 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438277 | GAAAAAGCAGTCTAT[C/T]TCATCTAGTTTTCAT | 25879 |
rs7833434 | snp | C/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415938 | GTGGATGTTGGAAGA[C/G]ACAAAGATGAATTTA | 25879 |
rs7835639 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434416 | CATGTAGAAATAAAG[C/T]ATCTTACTAAAAAGC | 25879 |
rs10093237 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423006 | TTTGGTGTAAAAAAA[A/G]AAAACTTATTTGCTG | 25879 |
rs10094939 | snp | G/T | 0.290718 | 0.246662 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432039 | GCTACTTTCTGTTGC[G/T]TCTTTGCTCCATCTA | 25879 |
rs10108112 | snp | A/T | 0.274393 | 0.248807 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422909 | TACAATTTGAAAGAT[A/T]GTCATGTGAAAAAGA | 25879 |
rs10112317 | snp | A/G | 0.290718 | 0.246662 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433487 | TGATAGATTCTTAAT[A/G]CATGTTTTTTTTAAG | 25879 |
rs10541932 | in-del | -/TAAA | 0.489722 | 0.0709447 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430392 | GCAAGACTCTGTCTC[-/TAAA]TAAATAAATAAATAA | 25879 |
rs10709873 | in-del | -/A | 0 | 0 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414677 | GCCAACGCGGACAGC[-/A]ACGCTCCCTTCAACG | 25879 |
rs11290677 | in-del | -/T | 0.396546 | 0.202545 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428907 | GTATTTGTTCAGCTG[-/T]TTTTTTTTTTAATTG | 25879 |
rs11985510 | snp | A/G | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416811 | tcagttTCTCCATCT[A/G]TAAAGATTCATTTTT | 25879 |
rs11985609 | snp | A/G | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417101 | TTTGCACAGTACCAT[A/G]TTAACTGAACCAGTC | 25879 |
rs12547432 | snp | G/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438927 | CACTTACTAATATAG[G/T]ATCACCTGTGAATTC | 25879 |
rs12675902 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435805 | GGTATGTGCCTACCA[A/G]TAAGCCATTTATATt | 25879 |
rs12677876 | snp | C/G | 0.346368 | 0.23068 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419877 | AGCTGGGCGTGGTGG[C/G]ATGCGCCTGTAATCC | 25879 |
rs13261525 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417536 | agtcacagctactca[A/G]gaggctgaggcggga | 25879 |
rs13272825 | snp | A/G | 0.00273758 | 0.0368957 | missense | DCAF13 | GRCh38.p7 | 8:103420402 | ACCGTGATGGAGTCA[A/G]TTGCTTGGCAAAGCA | 25879 |
rs13276522 | snp | G/T | | | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415424 | CGGACACCTCGTGGA[G/T]TCCGGCCGGAAGAGC | 25879 |
rs13278059 | snp | A/T | | | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415425 | GGACACCTCGTGGAG[A/T]CCGGCCGGAAGAGCA | 25879 |
rs13280790 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418869 | atatatatatatatT[G/T]TTttttttttttttt | 25879 |
rs13280792 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418875 | atatatatTTTTttt[G/T]ttttttttttttttt | 25879 |
rs13280803 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418884 | TTTtttttttttttt[G/T]ttttttttttttttt | 25879 |
rs13439598 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419142 | gtccgtcccggcccc[C/G]caaagtgctgggatt | 25879 |
rs16870396 | snp | A/G | 0.322483 | 0.239262 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426940 | GTCTTGTCTCATTAT[A/G]GTATTGTTTCCCCCT | 25879 |
rs17229709 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427761 | TGCTCAGAAGTCTGA[A/G]TTGTGATTCCCAGTT | 25879 |
rs17230038 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442253 | AAAAAATAATTTCTG[A/G]TGTAGCTGGAATTAA | 25879 |
rs17804088 | snp | A/G | 0.288386 | 0.247035 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426269 | AAGACTTTAGGCTGT[A/G]ATTGTTGACCCATTT | 25879 |
rs17804130 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426491 | CATCATAGATCTTAC[A/G]CAAAACTCAGAATTT | 25879 |
rs17804149 | snp | A/C | 0.274393 | 0.248807 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426881 | ATTTGTAGTTGGAAA[A/C]ACGTTAGTAATTTCT | 25879 |
rs17804400 | snp | C/T | 0.207559 | 0.246371 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436495 | CATAGAGTGTGATTC[C/T]AATATTTAAGATTTT | 25879 |
rs28445772 | snp | C/G | 0.0872718 | 0.189788 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418021 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 25879 |
rs28630640 | snp | C/T | 0.089084 | 0.191327 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414303 | GAAACTTGTACCATT[C/T]TACAAATGCCAAAAA | 25879 |
rs28716608 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430861 | TCAGCTCCCTATTGC[A/T]TTTTAGAGACTCTTA | 25879 |
rs33990406 | in-del | -/ACA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429691 | TATAGAGAGTTAACA[-/ACA]CGAAGAAACATTTAC | 25879 |
rs34000715 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431804 | TTTTTTTTTAATTTA[A/G]TTTATTTTTCATTGT | 25879 |
rs34003376 | in-del | -/AA | 0.02016 | 0.0983543 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435298 | TGAAAAAGGTTTTTT[-/AA]AAAATTATGCTGTAC | 25879 |
rs34121596 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425748 | GATATTATAATACCA[-/T]TTTTTTATAATCCAT | 25879 |
rs34151780 | in-del | -/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425919 | AGGTGGGATATAAAT[-/G]GGATCAATAAGTGTA | 25879 |
rs34487592 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431881 | TAATTTTAGGTTGAA[A/G]AAAATGTAGCCTGGC | 25879 |
rs34676422 | in-del | -/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439406 | TTTTTTTTTTTTTTT[-/T]GAGGCAGAGTCTCAC | 25879 |
rs34702662 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417660 | AAAAAAAAAAAAAAA[-/A]GAACATCTTTAATTA | 25879 |
rs34792510 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441376 | GATTAGGTTAGGGGG[-/A]AAAGGGTGCTTTCTA | 25879 |
rs34981671 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433163 | AGAAGTTGGCTGATG[-/T]TTTGATGTAGGTCTT | 25879 |
rs35111670 | in-del | -/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413819 | ATCTTCCACTGAACC[-/T]TAAAGATACACATGG | 25879 |
rs35207137 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423413 | CTTGCAGCATACATG[-/A]AATGAACCTGGAGGA | 25879 |
rs35579301 | in-del | -/AAAG | 0.491671 | 0.063992 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440085 | AGGCAGTGGTTACTC[-/AAAG]AAAATCTGTACCAAA | 25879 |
rs35598335 | in-del | -/T | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443185 | TGTAGACACTATACA[-/T]TTCAAATTGACATTT | 25879 |
rs35687556 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423956 | CTGTCTCAGCCTCCC[-/A]AAAAGTGTTGGGATT | 25879 |
rs35866941 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438421 | AGTATAGTCGAGAGA[-/T]TTTTTTTTTTTTTTT | 25879 |
rs35951748 | in-del | -/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439671 | AGATTCAGCATATCA[-/G]GGAGGTACTCTTTGA | 25879 |
rs35981625 | in-del | -/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426558 | AATAGTATTATGCAT[-/C]CATGTATAAATCTTA | 25879 |
rs36073721 | in-del | -/TAT | 0.48978 | 0.0707512 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440326 | TCTAATTTTATTAGA[-/TAT]TATTACATTATGAAA | 25879 |
rs55986900 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434561 | TGGTGTCTGCCAGGT[G/T]TCTCCACTAAAGAGT | 25879 |
rs56413813 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441809 | TTGAGACGGAGTCTC[A/G]CTCTGGAGTGCAGTG | 25879 |
rs56825753 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424633 | TTTGTACTCAGTAGA[C/T]GGCAGAACAGCTTGG | 25879 |
rs57204083 | in-del | -/G/GAAA | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440088 | CAGTGGTTACTCAAA[-/G/GAAA]ATCTGTACCAAAATC | 25879 |
rs57225658 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420023 | AAAAAAAAAAAAAAA[-/A]GGAAATGCTGCATGT | 25879 |
rs58480092 | in-del | -/AAAA | 0.344815 | 0.231323 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440394 | TGACATAGCTGTGAT[-/AAAA]AAAGCAATAAATGGA | 25879 |
rs58912311 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423876 | ATTTCCCCCCACTTT[A/T]TTTTTTTAAAGAGAC | 25879 |
rs59392618 | in-del | -/T/TT | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441795 | CTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTCGC | 25879 |
rs59753511 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425554 | CACAGTTTGAAAACC[A/G]CTGACTTAGTAGTTT | 25879 |
rs60025462 | in-del | -/TTA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440331 | TTTTATTAGATATTA[-/TTA]CATTATGAAAATTTA | 25879 |
rs60825382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436456 | GCTGTCCCATAGTCT[C/T]GTGTGTGTCTCATTT | 25879 |
rs61744470 | snp | C/T | 0.21875 | 0.248039 | missense | DCAF13 | GRCh38.p7 | 8:103421072 | GCTTTTGTGGGACTT[C/T]TTTTTTCACTGTAAG | 25879 |
rs62527062 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429159 | GGTGGCATTTGGTCT[A/G/T]GGTAGATTGTTTTGC | 25879 |
rs62527063 | snp | C/T | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443545 | TTTTAATCATCAACT[C/T]AATAAACTTTATTAT | 25879 |
rs71297204 | in-del | -/TTAT | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418853 | TATATATATATATAT[-/TTAT]ATATTTATATATATT | 25879 |
rs71575961 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441782 | GCCTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTG | 25879 |
rs72675463 | snp | A/G | 0.000849377 | 0.0205905 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421320 | TGGAATTAATGAGAG[A/G]TAAGTCTAGAAAGAG | 25879 |
rs72675464 | snp | A/T | 0.111224 | 0.207945 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423328 | GGATGAATGAATTTT[A/T]AAAAAAAAAGTACAC | 25879 |
rs72675468 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427401 | GTAAATGAGTTCTGA[C/T]ACCTTTGCTCAAATC | 25879 |
rs72675472 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429230 | GGTCAGACCCTGAGG[C/T]GACATAATGAGAAGC | 25879 |
rs72675482 | snp | C/T | 0.120326 | 0.21374 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436257 | CAGTTTAAGAAAAAT[C/T]AGTAATAATACTTTA | 25879 |
rs72675485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442106 | CAAAAAAGGGAAGCA[A/G]TGACTATCTGAGAAT | 25879 |
rs72675486 | snp | C/G | 0.0166325 | 0.0896639 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443443 | ATTAAAAGTTCCTTT[C/G]AGCATTGAAACTTTG | 25879 |
rs73287945 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415702 | TAGCAAGTAAAGTCT[A/G]TTCAAGTCCTTTTTC | 25879 |
rs73287947 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417164 | CACATCTGTTAACCA[C/T]GAAACTTTGCAAAGT | 25879 |
rs73287948 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417815 | GTGACATGTAAAAAG[C/G]TGTTTTAAGATGACA | 25879 |
rs73287951 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419588 | AGGAAGCTTAGAGTT[C/G]TGTTGAGCAAACATC | 25879 |
rs73287953 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421597 | AATAACTCCTCTGTC[C/T]CCTCAGTCCCCAACC | 25879 |
rs73287956 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424674 | GCAAATTCAGTCTTG[A/C]GCTTGCAGACACTAT | 25879 |
rs73287968 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432126 | AGGGATTGTAGTCCC[C/T]TACCAGGTACAGTTC | 25879 |
rs73287982 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437988 | GTAGAACTTTTGGTG[A/G]GCTTAATAAACTTAG | 25879 |
rs73299375 | snp | A/C | 0.000737133 | 0.0191839 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442771 | TCCCATAACTTGCTT[A/C]TATTTTGTATATTTT | 25879 |
rs73699799 | snp | C/T | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414564 | TTTTTTCTCAGACTT[C/T]TCTACATACATGCCC | 25879 |
rs74307462 | snp | A/G | 0.021333 | 0.101051 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425167 | TATCAAAAAGTGGAT[A/G]TAGATTGCATCTAAT | 25879 |
rs74451941 | snp | C/T | 0.0448719 | 0.142907 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443953 | GGTTGAGTCTATGGG[C/T]GAGGAACCCACAGAT | 25879 |
rs74512200 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427820 | TTGGCCACTACATGT[C/T]GTCTGTTTAGGTCTG | 25879 |
rs74611162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423286 | ACAATACCCAGGATA[C/T]GGAATCAACCTAAAG | 25879 |
rs74849822 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430848 | TAGTCATGTTCTTTC[A/G]GCTCCCTATTGCTTT | 25879 |
rs74880499 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433347 | TTTCAGTATCCATAT[A/G]AGGTAGGTGGGACAT | 25879 |
rs75121891 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431904 | AGCCTGGCTTTCAAG[A/G]TGCTCTGAAATCTGG | 25879 |
rs75480159 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423748 | TTCCACAGTGTCTAC[A/G]TGTATCAAAACACAA | 25879 |
rs75672537 | snp | G/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424035 | AAGATTTTTTTTTTT[G/T]TGAGATGAAGTCTCC | 25879 |
rs75968104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416080 | AAATTGTACTTTGTG[A/G]TACCTAAATGACAAG | 25879 |
rs76028359 | snp | A/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418862 | TATATATATATATAT[A/T]TATATTTTTTTTTTT | 25879 |
rs76471833 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412774 | ACCTCTGAGTTCCAA[C/T]TTATACTTGAACTCA | 25879 |
rs76530805 | snp | G/T | 0.000115166 | 0.00758748 | missense | DCAF13 | GRCh38.p7 | 8:103442872 | AACACGTAGTGGCAG[G/T]TGTAAAATAATTGGT | 25879 |
rs76920320 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420028 | AAAAAAAAAAAGGAA[-/A]TGCTGCATGTATATA | 25879 |
rs76966915 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437600 | TGTTAACGTCCTGTT[G/T]TGTTTAGATATAAAT | 25879 |
rs77139843 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422216 | TTTTGAAGGGTGGCA[A/G]TGGGAAGGATATGAT | 25879 |
rs77441025 | snp | A/C/G | 0.00692715 | 0.0584537 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440105 | TCTGTACCAAAATCC[A/C/G]AAGGGTTTTAACTTA | 25879 |
rs77639487 | snp | A/G | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416301 | GTGTGAGCATTGCTA[A/G]TAAGTCTCTGCTCAA | 25879 |
rs78192721 | snp | A/C | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420007 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 25879 |
rs78218921 | snp | A/C | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417962 | ATCTCTACTAAAAAT[A/C]CAAAAAAATAAATAA | 25879 |
rs78552259 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422611 | GTAGAGATGTAAAAA[A/G]TAGAAAATTAAAGAT | 25879 |
rs78879352 | snp | A/T | 0.00668924 | 0.0574445 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440102 | AAATCTGTACCAAAA[A/T]CCAAAGGGTTTTAAC | 25879 |
rs79033615 | snp | A/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418870 | TATATATATATATTT[A/T]TTTTTTTTTTTTTTT | 25879 |
rs79118126 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432931 | TTATTTCGTCAGTAT[A/T]TAGAATGATGTAGAC | 25879 |
rs79466283 | snp | A/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418854 | TATATATATATATAT[A/T]TATATATATATATTT | 25879 |
rs79707846 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432971 | TAAACAACTCGTGGA[C/T]CAAATCCTTTCTGTT | 25879 |
rs79854865 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418709 | AGATATAACACCATT[A/G]CCAGGGAGTCAGAAA | 25879 |
rs80030128 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427965 | TAGGGATATGTTTTT[C/T]CTGTTGAAAGAAAAG | 25879 |
rs80108436 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439612 | CAGGCTGGTCTAATT[A/T]ATTAAGCTTTTTAAA | 25879 |
rs111390264 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418840 | TATATATATATATAT[A/G]TATATATATATATAT | 25879 |
rs111546685 | snp | G/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431022 | GTAATAATATTCAAA[G/T]AATATTCAATAAATT | 25879 |
rs112279735 | in-del | -/G | 0 | 0 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413006 | TTTCACAGCTACACT[-/G]TGAGCTTTATTATTA | 25879 |
rs112338530 | snp | G/T | 0.119978 | 0.213528 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419018 | CCTCCTGAGTAGCTG[G/T]GACTGCAGGCACATA | 25879 |
rs112664868 | snp | A/C | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436323 | GTATGCCAAACCAAA[A/C]ATTAAAAAAGAAATA | 25879 |
rs112926645 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414049 | ATAAATCAAGTGAAC[G/T]GAATTGCCTAATGCT | 25879 |
rs113065425 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426336 | AAAGAATTTTAACAG[-/T]TTTTTTTTTTTTTGG | 25879 |
rs113087306 | snp | A/C | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438950 | GTGAATTCTTCTAGC[A/C]TATTTCACAGCCTTT | 25879 |
rs113108933 | snp | C/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441124 | CTCTTTACCCACCCC[C/T]AAAATTTGAGTGAGT | 25879 |
rs113343355 | snp | C/T | 0.5 | 0 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441580 | TATCTATAGCCAGAT[C/T]CAGGAACAGCGCATC | 25879 |
rs113367023 | in-del | -/ATT | 0.375 | 0.216506 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440330 | ATTTTATTAGATATT[-/ATT]ACATTATGAAAATTT | 25879 |
rs113982059 | snp | C/T | 0.5 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442553 | TCACTTTTAGAAATT[C/T]TATTAACTGTGGAAG | 25879 |
rs113982117 | snp | C/T | 0.00388579 | 0.0439067 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426112 | GCCAGGCTATGGAGA[C/T]GAGGAAGAGCCATTA | 25879 |
rs114074196 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420707 | TTAAAGTATTTAAGT[A/G]TGAGTTTTTTCACAG | 25879 |
rs114156661 | snp | C/T | 0.489665 | 0.0711382 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414682 | CGCGGACAGCAACGC[C/T]CCCTTCAACGCTCCT | 25879 |
rs114231756 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434354 | TTTAAAGGTTTTCCA[G/T]GTACACAAATTGATA | 25879 |
rs114300131 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432521 | TGTATTTAAGAAGCA[A/G]TTACTGATTGATTTC | 25879 |
rs114318660 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442287 | ATTTTGTGTATTTTC[A/C]AAGTTAAAGAATTAA | 25879 |
rs114417871 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423468 | GATACCACATGATCT[C/T]AGTTGTGTGGAATCT | 25879 |
rs114430486 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421477 | CTCTGTTTTTAAATA[C/T]ACAGTTTGGTGGCAT | 25879 |
rs114521501 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412754 | ATCTTTCTACCACTC[C/T]GGACACCTCTGAGTT | 25879 |
rs114768957 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414293 | TTTTTTCACAGAAAC[C/T]TGTACCATTCTACAA | 25879 |
rs115081944 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422455 | AATGCCCACCTCTGG[A/G]AAGTGGGAAAACTCT | 25879 |
rs115109722 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434402 | CTTATCATTTTTCCC[A/T]TGTAGAAATAAAGCA | 25879 |
rs115305690 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436736 | TGTATAGTGAATTAT[A/G]GTTTACAAAGAGCTG | 25879 |
rs115331847 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439918 | TTATTTCTCTTACTA[G/T]ATAGTAAGTTCTCTG | 25879 |
rs115332818 | snp | C/T | 0.00569052 | 0.0530366 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415222 | ACAAATGCTCCAGCC[C/T]ACGGACGCGGAAGCG | 25879 |
rs115361595 | snp | A/G | 0.0205511 | 0.0992634 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413652 | ATTATTTGTGCATGC[A/G]TCATAAAACTTCATG | 25879 |
rs115365079 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437458 | AAGCTAGTGTGGACA[C/G]CTAAATGTAGGTCTA | 25879 |
rs115393786 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416088 | CTTTGTGATACCTAA[A/G]TGACAAGGGACCAAC | 25879 |
rs115398259 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425020 | CAAAACCTTTCCTGA[A/T]CACTTATCTGTTTTC | 25879 |
rs115564917 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426856 | GGGGTATGAGTATGA[A/G]GTAGAGATAATTTGT | 25879 |
rs115669004 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420699 | GTTTATAATTAAAGT[A/C]TTTAAGTATGAGTTT | 25879 |
rs115710822 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426883 | TTGTAGTTGGAAACA[C/T]GTTAGTAATTTCTAA | 25879 |
rs115908581 | snp | A/T | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415642 | TCAGTTACCTTTCGC[A/T]AAGGCAAACTTTGTG | 25879 |
rs116022201 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437591 | CTTAATATGTGTTAA[C/T]GTCCTGTTGTGTTTA | 25879 |
rs116023130 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413775 | AGCTGTCAAAATATT[A/G]GCCCTTCTATGGGAA | 25879 |
rs116080014 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433133 | TGAAAATGTTTAACA[C/T]TTGGCCCTTTACAGA | 25879 |
rs116080932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442664 | AGCTTCCTTTTACCT[A/G]TTGTCATCGTGAAAA | 25879 |
rs116473907 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423125 | TGTTGTGCAAGGAAT[G/T]GATTGGCAAGTGGGA | 25879 |
rs116568816 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425925 | GGATATAAATGGATC[A/G]ATAAGTGTAATACTG | 25879 |
rs116729967 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434502 | GTAAAGCAGTTGTCA[A/G]TGTCTTACTACTAGT | 25879 |
rs116761757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425333 | TAAACATGTCTGCCA[A/G]ATACCCATGTCTAAA | 25879 |
rs117649686 | snp | A/G | 0.010581 | 0.0719621 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432619 | GTGGGGAAAAGAAAA[A/G]GAAAGGAAGTGGGAA | 25879 |
rs117739694 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422973 | CTGGAAATAGGTGTT[A/C]GTGTTAAAAGATTCG | 25879 |
rs118074319 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424016 | TGTTTCTCGGTTTTT[C/T]AAAAAGATTTTTTTT | 25879 |
rs137924177 | snp | C/G/T | 9.98463e-05 | 0.00706505 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415415 | AACTCCTAGCGGACA[C/G/T]CTCGTGGAGTCCGGC | 25879 |
rs137932701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416503 | CAGTGCGTTTCAGTC[A/G]TCTTTTTTAAGGCCT | 25879 |
rs137959121 | snp | C/T | 0.000333167 | 0.0129024 | missense | DCAF13 | GRCh38.p7 | 8:103432699 | CAATCTGTTGGAACC[C/T]TATGGAAGCTTTCAT | 25879 |
rs138157301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425728 | ATTTTTTTGAATGAC[G/T]AACCAGATATTATAA | 25879 |
rs138240593 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415243 | CGCGGAAGCGACTGC[A/G]CAGCTAAAGAACCGC | 25879 |
rs138283561 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419957 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 25879 |
rs138536020 | snp | G/T | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103435711 | CTTGATGTGGATTAC[G/T]CTCCCACTGGGAAGG | 25879 |
rs138554712 | snp | C/T | 1.69476e-05 | 0.00291093 | utr-variant-5-prime, splice-donor-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414783 | CTGGGCGGGCTCTTA[C/T]CGGCGAAGCGGATCT | 25879 |
rs138800866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420661 | AGTTTAAGGATCAAT[G/T]TGACAGTAAATTAAA | 25879 |
rs138804549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436017 | TTACTGTGCTGAATA[C/T]TGTGGGCAATTGTAA | 25879 |
rs138974900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428800 | TGCTTTGGTGAACAT[A/C]TGTGTCAGAAGAGCC | 25879 |
rs138978000 | in-del | -/TT | 0.02016 | 0.0983543 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425560 | TTGAAAACCACTGAC[-/TT]AGTAGTTTCTGCAGT | 25879 |
rs138994351 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424746 | CTCAGGGACACAGTT[C/T]ATCCTGTATTCTGTA | 25879 |
rs139057671 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435279 | ATGTATTTAAATAGT[A/T]TGGTGAAAAAGGTTT | 25879 |
rs139069337 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442058 | TGTGAGCCACCATGC[C/T]CCGCCCAGAAGGCCA | 25879 |
rs139096038 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429872 | AAATAATTAGCCCTA[A/C]ATATCAAAAGCCATA | 25879 |
rs139154337 | in-del | -/T/TT | 0.0205511 | 0.0992634 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422997 | GATTCGGTTTTGGTG[-/T/TT]TAAAAAAAAAAAACT | 25879 |
rs139166044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421767 | ACATAATTGTCTTCA[A/G]GGTTTATCCATGTTG | 25879 |
rs139175200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437050 | TCAGTTAGAAGCATA[C/T]TGACAGGAGTGTTCT | 25879 |
rs139201908 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414678 | CCAACGCGGACAGCA[-/AC]GCTCCCTTCAACGCT | 25879 |
rs139251262 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413654 | TATTTGTGCATGCAT[C/G/T]ATAAAACTTCATGAC | 25879 |
rs139400754 | snp | C/T | 0.00146931 | 0.0270647 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103440232 | TGATGAAATGAACAT[C/T]CGCCTGTGGAAAGCT | 25879 |
rs139565021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418436 | GAGGTGAGAGGCTAA[A/G]GTGGGAGGATCACTT | 25879 |
rs139663657 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425912 | CTAAAACAAGGTGGG[A/T]TATAAATGGATCAAT | 25879 |
rs139851019 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432195 | GTGGCAAAACATCCT[A/G]CAGTGGATAGTCATA | 25879 |
rs139907413 | snp | A/G | 0.000181277 | 0.00951871 | missense | DCAF13 | GRCh38.p7 | 8:103441615 | AAGAAGCTCGTCGAC[A/G]AAAGTATGTTTTGAG | 25879 |
rs140032545 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417763 | GAAAGTTTGAAGACT[A/G]CTATATAGGGAGCCT | 25879 |
rs140127381 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427642 | AAGAAGGAGCATTGG[A/G]CATCATTTTGTCTAT | 25879 |
rs140179211 | snp | A/C/G | 0.00103137 | 0.0226863 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415122 | TGAGGGGGCAAGAAC[A/C/G]GGGCACAGACACTAC | 25879 |
rs140398410 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416064 | CATGCTAACCACTTA[C/T]AAATTGTACTTTGTG | 25879 |
rs140519539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431302 | AGTAAGGAAAGGAGT[A/G]CCATTGTAAGTAAAA | 25879 |
rs140524999 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415145 | GACACTACGTCACGC[C/T]GGCGGAAAGCGCGAT | 25879 |
rs140560341 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426825 | AGACTAAATGTTCTT[A/C]AAGGGATAGGGGAAT | 25879 |
rs140680400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432579 | TTACACATAATAGGT[A/G]TTTATGAAATATTTG | 25879 |
rs140699787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429127 | TGCTGATCATTGGGA[C/T]GTTTTACAGTGTGAA | 25879 |
rs140817247 | snp | A/G | 0.000148884 | 0.0086267 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420451 | TGTCCTTTCTGGGGC[A/G]TGTGATGGAGAGGCA | 25879 |
rs140915485 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428652 | AAAGTTGATAACATA[C/T]GTGAACATTTTTTAA | 25879 |
rs140939054 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413103 | GTCACCTCAGCCCCA[C/T]TAGTCTCCTAATACT | 25879 |
rs141081528 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439108 | CGCCTCCTGGGTTCA[C/T]GCCATTCTGCCTCAG | 25879 |
rs141131174 | snp | A/G | 0.00024751 | 0.0111218 | missense | DCAF13 | GRCh38.p7 | 8:103435748 | TGTCTGCTAGTTTCG[A/G]TAAATCTATTCGAAT | 25879 |
rs141207268 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419408 | GTTAAGGTTTTTGGA[A/G]CAGCGCCTGGCACTT | 25879 |
rs141239140 | snp | C/G/T | 0.00137272 | 0.0261634 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415324 | GAGCCAGCAGGCCGC[C/G/T]GCTCCGCGAGTCACG | 25879 |
rs141290873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436148 | ATTGACCAAAATGTC[A/G]TATGACTATTTTTGT | 25879 |
rs141364539 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423303 | GAATCAACCTAAAGT[A/G]TCCAGCAATGGATGA | 25879 |
rs141399531 | in-del | -/AGT | 0.00993419 | 0.0697739 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433583 | ATTTGGAAGCAAAAA[-/AGT]AGTAGTGTTAGCTCA | 25879 |
rs141495905 | snp | C/T | 9.92901e-05 | 0.00704522 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426103 | AATGGATGGGCCAGG[C/T]TATGGAGACGAGGAA | 25879 |
rs141568647 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413251 | GATCACCTCGACTAT[C/T]ACCTCTTCTGCTCCT | 25879 |
rs141572440 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439590 | GACAAGGTTTCACCA[C/T]GTTGGGCAGGCTGGT | 25879 |
rs141623332 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423323 | CAATGGATGAATGAA[-/T]TTTTAAAAAAAAAAG | 25879 |
rs141706261 | in-del | -/AG | 0.0186012 | 0.0946287 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440852 | TTTTCTATAAGAAAC[-/AG]AGTGTTTATATTAGA | 25879 |
rs141779934 | snp | A/G | 0.00354785 | 0.0419683 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441460 | GTATTTTCAGCTTAC[A/G]TCACGAGAAAAAGCA | 25879 |
rs141948809 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421879 | CATCAATGAGCATTT[C/G]ATTTGTTTCCACCTT | 25879 |
rs141965384 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428917 | AGCTGTTTTTTTTTT[A/T]AATTGCTATTAACCT | 25879 |
rs141990122 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420709 | AAAGTATTTAAGTAT[C/G]AGTTTTTTCACAGAT | 25879 |
rs142248983 | snp | C/G/T | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424964 | AAGGATTCTGTTCAT[C/G/T]GACATCCTCAACAAA | 25879 |
rs142266909 | snp | C/G | 0.000167356 | 0.00914603 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415252 | GACTGCACAGCTAAA[C/G]AACCGCCCCTTGCTA | 25879 |
rs142367101 | snp | A/C/T | 0.00319735 | 0.0398564 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415200 | GAGTCTCCGCCCTGC[A/C/T]TCGCCCACAAATGCT | 25879 |
rs142400258 | snp | C/T | 8.25525e-05 | 0.00642413 | missense | DCAF13 | GRCh38.p7 | 8:103420285 | GAAACTATGATCCTG[C/T]TTTACATCCTTTTGA | 25879 |
rs142463527 | snp | A/G | 3.51747e-05 | 0.00419358 | missense | DCAF13 | GRCh38.p7 | 8:103435646 | ATACTTTTGATATGC[A/G]TGCACTGGACACTCC | 25879 |
rs142531067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431764 | TCATTTCTGCCCCCT[C/T]CCACCTACCTAACAC | 25879 |
rs142773284 | snp | A/G | 3.67121e-05 | 0.00428424 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442822 | TATTAAACACAGCAA[A/G]CCTGGATCTGTGCCA | 25879 |
rs142883204 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421639 | CTATTTTACTTTTTG[A/C]CTCTGTGATTTTGAC | 25879 |
rs142903463 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438917 | CCTTTCTTAACACTT[A/G]CTAATATAGTATCAC | 25879 |
rs143025416 | snp | A/G | 0.00152733 | 0.0275922 | missense | DCAF13 | GRCh38.p7 | 8:103420431 | CATCCAGAGAAGCTG[A/G]CTACTGTCCTTTCTG | 25879 |
rs143071451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435414 | ATTTATAGGGTGGAA[A/G]ATGTGTTGGTATATA | 25879 |
rs143111078 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429965 | TCAAAAGAAGAACTA[C/T]GTGGGGGGGAAATGT | 25879 |
rs143211923 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434734 | GTATTACTTTTGTCC[A/G]TTGTTCATGTTGGTT | 25879 |
rs143287205 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432356 | TCACCATTAATTTTG[C/T]CCCTAATTTGATACT | 25879 |
rs143489153 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417017 | ATTAAATATATTAAA[G/T]AAACGTGGCCAATTA | 25879 |
rs143528036 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412855 | CCACACCCTGTCATC[A/T]TTAGATTTTAACTTT | 25879 |
rs143536359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440762 | TAGCAGGTGTTATCA[C/T]TGGCTGGTTACCTCC | 25879 |
rs143548999 | snp | G/T | 4.95315e-05 | 0.00497627 | missense | DCAF13 | GRCh38.p7 | 8:103427197 | GAACTAATCCTATAT[G/T]TTCAATGACCTGGGG | 25879 |
rs143980576 | snp | C/T | 1.80896e-05 | 0.0030074 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415067 | CAACGAGAGGACTCT[C/T]ATGCCCAAGGCGCGT | 25879 |
rs144155480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422274 | TTCGAGTGAAGATGT[C/G]TGTCATACCTTTACA | 25879 |
rs144301160 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425910 | TACTAAAACAAGGTG[G/T]GATATAAATGGATCA | 25879 |
rs144319160 | snp | A/G | 0.000447146 | 0.0149457 | missense | DCAF13 | GRCh38.p7 | 8:103442862 | GAGAAGAAGAAACAC[A/G]TAGTGGCAGTTGTAA | 25879 |
rs144470699 | snp | A/C | 0.000237312 | 0.0108904 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414823 | CGAGCGGATGCAGCG[A/C]AAGGTTGGATAAGAC | 25879 |
rs144536229 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427381 | TTTTGTCAGTTTTCC[C/T]GATTGTAAATGAGTT | 25879 |
rs144553536 | in-del | -/AAC | 0.277334 | 0.248501 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429687 | AATTTATAGAGAGTT[-/AAC]AACACGAAGAAACAT | 25879 |
rs144632227 | snp | C/G | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103435668 | GGACACTCCTGTAAT[C/G]GTCCATATGGATCAT | 25879 |
rs144637688 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431597 | TCCTATATGAACTTT[A/G]GTCTTAGACTTTTAA | 25879 |
rs144660563 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103421026 | CGTACAATACAAGCA[C/T]ATGAAGGCTTTGTAC | 25879 |
rs144723655 | snp | A/G | 4.94197e-05 | 0.00497066 | missense | DCAF13 | GRCh38.p7 | 8:103441570 | TACCAAAATCTATCT[A/G]TAGCCAGATTCAGGA | 25879 |
rs144834191 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417368 | GATCTTTGGCTGGGC[A/C/G]TGGTGGCTTATGCCT | 25879 |
rs144904194 | snp | A/C | 0.00597247 | 0.0543191 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443805 | GATTACTTATAATAC[A/C]TAATACAATGTAAAT | 25879 |
rs144972779 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428158 | GTTTGTATGATATAC[C/T]GGAAAATGAGATGCT | 25879 |
rs145084245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428763 | TTACTATTTAGAGGA[A/G]CAAAAAAATCTTTTG | 25879 |
rs145160697 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424278 | GTGATCCACCCGCCT[C/G]AGCCTCTGAAAGTGC | 25879 |
rs145230539 | snp | C/G | 0.00261182 | 0.0360429 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415196 | TCCCGAGTCTCCGCC[C/G]TGCCTCGCCCACAAA | 25879 |
rs145286318 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421860 | TTTTGTTTATCCGTT[A/C]ATTCATCAATGAGCA | 25879 |
rs145431574 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433161 | AGAAGAAGTTGGCTG[A/G]TGTTTGATGTAGGTC | 25879 |
rs145461593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422335 | AGAGCTGAACTTGAC[A/G]TCATCAATATAGAAC | 25879 |
rs145609503 | snp | C/G | 4.95103e-05 | 0.00497521 | missense | DCAF13 | GRCh38.p7 | 8:103427157 | GCCACATGTGGACAG[C/G]AAGTAGACATTTGGG | 25879 |
rs145866099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419184 | CCACCACGCCCGGCC[C/T]TAAGCGTGATTATTA | 25879 |
rs145901227 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417162 | ATCACATCTGTTAAC[C/G]ACGAAACTTTGCAAA | 25879 |
rs145930039 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437831 | ACTACAGTTAAGTCA[C/G]TATTTGAAAGTAGGC | 25879 |
rs145936328 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420301 | TTTACATCCTTTTGA[A/G]GTCCCACGAGAATAT | 25879 |
rs146039219 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441664 | CTTTTCTGACTTCTG[C/T]TCTCATCTCACCAAA | 25879 |
rs146051371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417719 | GAGAAGGGATCTGCT[C/T]AAAAACTCTGTTATT | 25879 |
rs146161228 | snp | A/G | 8.63386e-05 | 0.00656977 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415111 | GACTCTAGTACTGAG[A/G]GGGCAAGAACGGGGC | 25879 |
rs146162905 | snp | C/T | 0.000233832 | 0.0108102 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420442 | GCTGGCTACTGTCCT[C/T]TCTGGGGCGTGTGAT | 25879 |
rs146186495 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441959 | TTTAGTAGAGACAGG[G/T]TTTCACCATGTTAGC | 25879 |
rs146206587 | in-del | -/TCT | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412964 | TTATTTCGTTATTCA[-/TCT]TCTTAAGTTTTCCTC | 25879 |
rs146305428 | snp | A/G | 0.00372586 | 0.0430005 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420971 | CTGGTATGCCTTATC[A/G]TAGGTTAGAATTTGG | 25879 |
rs146475888 | snp | C/T | 0.0144049 | 0.083638 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415126 | GGGGCAAGAACGGGG[C/T]ACAGACACTACGTCA | 25879 |
rs146549010 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414587 | ACATGCCCCCTCTCT[C/T]AGTCTTGAGGAGCGG | 25879 |
rs146710116 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438521 | GTCTTCTGGGCTCTA[A/G]TGATCCTCCTACCTC | 25879 |
rs146842933 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432478 | TGGGAGTTAAGCATT[G/T]CTATTTTTATATTTA | 25879 |
rs146918818 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416400 | TGGCATCGTTCCCAG[A/T]CCTTGAATCTCTGGT | 25879 |
rs147014888 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419085 | TAGATGGGATTTCAC[C/T]GTGGTAGCCAGGATG | 25879 |
rs147061125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439970 | CCCCAGCACTTAACA[A/C]GGAACCTTATTAGTT | 25879 |
rs147070978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435985 | GTTGCTTCTAGACTA[C/T]GAATCTGTTCAGCAT | 25879 |
rs147137436 | in-del | -/ATAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430403 | TCTCTAAATAAATAA[-/ATAA]ATAAATAAAATACAA | 25879 |
rs147184833 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430000 | TGAAGTATTACTTAT[A/G]ATAGTAAAAAACAGG | 25879 |
rs147194382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426459 | TCAGAAAATGCTTCA[C/G]CTTGTCTAGTTGATG | 25879 |
rs147225637 | in-del | -/GGG | | | cds-indel | DCAF13 | GRCh38.p7 | 8:103442870 | AAACACGTAGTGGCA[-/GGG]GTTGTAAAATAATTG | 25879 |
rs147292370 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413040 | AGTCCTGCTTCCACT[C/T]CTGGATCTTTAATTT | 25879 |
rs147296877 | snp | A/G | 0.000395335 | 0.0140539 | missense | DCAF13 | GRCh38.p7 | 8:103441534 | ATCCTCATATAAAAC[A/G]TATAGCTCGTCATCG | 25879 |
rs147558721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419117 | TCTCGATCTCCTGAC[C/T]TCGTGATCCGTCCGT | 25879 |
rs147654325 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421864 | GTTTATCCGTTCATT[C/T]ATCAATGAGCATTTG | 25879 |
rs147702860 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430961 | TCTAATTAATACTTA[-/C]TGAATTGAAAGTTCT | 25879 |
rs147879440 | snp | A/C | 9.8868e-05 | 0.00703024 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421046 | AGGCTTTGTACGAGG[A/C]ATATGTACTCGCTTT | 25879 |
rs147969065 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443849 | TTGTTATACTGTATT[A/G]TTTAGGGAATAATGA | 25879 |
rs148038403 | snp | G/T | 0.00419407 | 0.045601 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441432 | CACACTATTCATTAA[G/T]ATACCAAAATGTGTA | 25879 |
rs148081663 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429273 | AGGGACCTCACTAGG[C/G]AAGTCTCAGAAAAGC | 25879 |
rs148135701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423261 | TAAAGGCTCATTTGC[A/G]GCATTATTCACAATA | 25879 |
rs148230364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419222 | CAATGTGTTTAGCAG[C/T]GTATCAGGACAGTTA | 25879 |
rs148247595 | snp | C/G | 0.00127433 | 0.02521 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415316 | ATCCAGTTGAGCCAG[C/G]AGGCCGCCGCTCCGC | 25879 |
rs148401929 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431638 | CTAAAATGTGTTTCT[C/T]CTGTAAGGTGGTGGT | 25879 |
rs148406806 | snp | A/C | 3.66026e-05 | 0.00427784 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415062 | GGGACCAACGAGAGG[A/C]CTCTTATGCCCAAGG | 25879 |
rs148445668 | in-del | -/TTA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440329 | AATTTTATTAGATAT[-/TTA]TACATTATGAAAATT | 25879 |
rs148522275 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421462 | AACGTAAAATTTACT[C/G]TCTGTTTTTAAATAT | 25879 |
rs148558263 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438669 | CAAAGTACTGGGATT[A/G]TAGGCATGAGCCACT | 25879 |
rs148779080 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443048 | GATCCTTAAAGGTGG[A/C]CTAGTTGGTAAGACT | 25879 |
rs148842547 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422365 | CTAATCATTGAAGCC[A/G]TAGTATGGCATCATT | 25879 |
rs148884091 | snp | C/G | 0.000198023 | 0.00994848 | missense | DCAF13 | GRCh38.p7 | 8:103427163 | TGTGGACAGCAAGTA[C/G]ACATTTGGGATGAAC | 25879 |
rs149094412 | snp | A/G | 3.61579e-05 | 0.00425178 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415514 | AGTTGGACTTACAGA[A/G]AGGTAAGATAAGTTG | 25879 |
rs149167193 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440541 | ATATTGAGTCTTACT[C/G]GTTTTTTGTGTTTTC | 25879 |
rs149220261 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434547 | TCATTTGGTTAGGGT[A/G]GTGTCTGCCAGGTTT | 25879 |
rs149273860 | snp | A/G | 1.69072e-05 | 0.00290746 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414810 | ATCTTCACGAGGTCG[A/G]GCGGATGCAGCGCAA | 25879 |
rs149319550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431465 | AAATCATTTTTATAA[C/T]GTAACAACTAGATAT | 25879 |
rs149416057 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417199 | AATTGATTCCAGTAT[A/G]CAACCCGTCCCGTTA | 25879 |
rs149431013 | snp | C/T | 0.000334197 | 0.0129223 | missense | DCAF13 | GRCh38.p7 | 8:103420389 | TCGCTGGATGGTCAC[C/T]GTGATGGAGTCAATT | 25879 |
rs149585075 | snp | A/G/T | 0.00358923 | 0.042236 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425877 | TTTTATGTACTTTAT[A/G/T]TATTTGTCACAAATC | 25879 |
rs149742593 | in-del | -/AAA | 0.0178098 | 0.0926698 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418544 | TCTCAAAACAAAAAC[-/AAA]AACAAAACACAAAAA | 25879 |
rs149909741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442555 | ACTTTTAGAAATTTT[A/G]TTAACTGTGGAAGGT | 25879 |
rs149993252 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414124 | ACTTGTAATAACTTT[A/T]TTTGGAAACTATTTT | 25879 |
rs150014655 | snp | C/T | 1.69163e-05 | 0.00290824 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415182 | GAGGTCCCAGCCTCT[C/T]CCGAGTCTCCGCCCT | 25879 |
rs150217408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429526 | GAATGATGCTACAGA[C/G]AGAGGGTTTCAGGGA | 25879 |
rs150274744 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439329 | CTTATCAGACACTTC[G/T]GTAGTCCTCCCTTCC | 25879 |
rs150482626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432804 | TTAATTGTATAAGTC[A/G]TACTAATAAAATATA | 25879 |
rs150763154 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421669 | CTATTCTGGGTACCT[C/T]ATATAAATAGAAGCA | 25879 |
rs150795428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436884 | TCATGGTCATAGTCA[A/G]TCTGCTTATCTAACT | 25879 |
rs150817520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425027 | TTTCCTGATCACTTA[G/T]CTGTTTTCATCTCAT | 25879 |
rs150911790 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413595 | TAGTTCACTGCCTTG[C/T]TCCTAGTAAATACTC | 25879 |
rs150914726 | snp | C/G | 0.00112163 | 0.023655 | missense | DCAF13 | GRCh38.p7 | 8:103435764 | TAAATCTATTCGAAT[C/G]TTTCCTGTAGACAAA | 25879 |
rs150932235 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431797 | ATTCTGTTTTTTTTT[A/T]AATTTAGTTTATTTT | 25879 |
rs151090071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439030 | TTTCTTTTTTTGAGA[A/T]GGAGTCTTGCTCTGT | 25879 |
rs151133774 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427456 | TCCCAGATACTAGAG[G/T]TAAGCATTGTTAGAG | 25879 |
rs151232952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415773 | TAGTGGAGAAAAATT[A/C]CAGCTGCTGCTCTGG | 25879 |
rs180776805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442177 | GGACAAACGATGAAA[A/G]TGAGTTACCAAAATA | 25879 |
rs180798162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431571 | CTCATTCATGTGATT[A/T]AATGGGAAGATCCTA | 25879 |
rs180809520 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424586 | TTCTATAAAATGAGA[A/C]AACCCTTCCCAGAAT | 25879 |
rs180832698 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413725 | CATAATTTTCGATGA[C/T]TTTCCTTCATAGAAC | 25879 |
rs181088314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415697 | ATGGATAGCAAGTAA[A/G]GTCTGTTCAAGTCCT | 25879 |
rs181097532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423974 | AAGTGTTGGGATTAC[A/C]GGCATGAGTCACCAT | 25879 |
rs181097654 | snp | A/G | 0.000372232 | 0.0136373 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441443 | TTAAGATACCAAAAT[A/G]TGTATTTTCAGCTTA | 25879 |
rs181153236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433650 | CAACTAAAAGCATCT[C/T]TTATGACTTTCTGCT | 25879 |
rs181239259 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437518 | TATAAAAGGGTTCTT[A/G]TATTTCATTTCTAAG | 25879 |
rs181321070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420039 | GGAAATGCTGCATGT[A/G]TATATACCTAGGGTC | 25879 |
rs181441287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427920 | TCTTAATGCATAACA[A/G]TAGATGAACTGATTG | 25879 |
rs181466879 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436878 | GGATGATCATGGTCA[C/T]AGTCAATCTGCTTAT | 25879 |
rs181485009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419732 | ATATAAAAGGGAGGC[C/T]GGGCACGGTGGCTCA | 25879 |
rs181708537 | snp | C/T | 0 | 0 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429448 | CTGCCCACATACTTG[C/T]AATAGGAAGTAATTG | 25879 |
rs181829366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428894 | CTGTATAGCAGCTGT[A/G]TTTGTTCAGCTGTTT | 25879 |
rs181948989 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442378 | CATCTATCATTTTGG[A/C]TATAGAGCAGAGCTA | 25879 |
rs182125746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416380 | TTAGATTTGTCACTT[A/G]GATTTGGCATCGTTC | 25879 |
rs182198013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434259 | ATTTAAACTAACTCT[A/G]TATCATAGTTTCAGC | 25879 |
rs182300985 | snp | A/T | 0.000245661 | 0.0110802 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432790 | CTATCATGAATGGCT[A/T]AATTGTATAAGTCGT | 25879 |
rs182316549 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430377 | AGCCTGGGTGACAGA[A/G]CAAGACTCTGTCTCT | 25879 |
rs182570628 | snp | A/G | 1.78353e-05 | 0.00298619 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415076 | GACTCTTATGCCCAA[A/G]GCGCGTGAGCGAAGC | 25879 |
rs182685807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439545 | AGGTGTGTGCCACCA[C/T]GCCCAACTAACTTTT | 25879 |
rs182820472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426307 | ATTTAATGCAGCTAA[A/C]GTCCTTTGATGCTAA | 25879 |
rs182837795 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426420 | CATTTCCCATGGGAA[C/G]ACCACGGAGAAAAAG | 25879 |
rs183019447 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439226 | TCGATCTCCTGACCT[C/T]GTGATCCACCTACTG | 25879 |
rs183037765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421400 | TTTGTTAGTCAGATA[A/G]TAAGGAATCATCGAA | 25879 |
rs183041652 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429863 | TCTTTGGAAAAATAA[A/T]TAGCCCTAAATATCA | 25879 |
rs183154832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417420 | GCCGAGACGGGCGGA[C/T]CACGAGGTCAGGAGA | 25879 |
rs183280114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422410 | AGGAAAATATAGAAA[C/T]ACAAAGATGTCAAGG | 25879 |
rs183410656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425962 | TATGGTATGTTACCT[C/G]TTTTAAACAAGATAC | 25879 |
rs183706608 | snp | A/T | 8.23825e-05 | 0.00641751 | missense | DCAF13 | GRCh38.p7 | 8:103421031 | AATACAAGCACATGA[A/T]GGCTTTGTACGAGGA | 25879 |
rs183746216 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436363 | TTAAATTGTCAAGAC[A/C]GTTCTCCCTCTATTT | 25879 |
rs183757080 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418072 | GGTGGAGCTTGCAGT[A/G]AGCCGAGATTGCGCC | 25879 |
rs183885701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431802 | GTTTTTTTTTTAATT[C/T]AGTTTATTTTTCATT | 25879 |
rs183901756 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414467 | GATTTGCACGTGTGA[A/G]GACTAAACCTTAAAA | 25879 |
rs183906769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435285 | TTAAATAGTATGGTG[A/G]AAAAGGTTTTTTAAA | 25879 |
rs183927250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438284 | CAGTCTATCTCATCT[A/G]GTTTTCATTTTAATA | 25879 |
rs184067337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417219 | CCGTCCCGTTAATAC[A/C]GTACAGTGCGAAAGT | 25879 |
rs184208376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440542 | TATTGAGTCTTACTG[G/T]TTTTTTGTGTTTTCC | 25879 |
rs184259950 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413107 | CCTCAGCCCCACTAG[G/T]CTCCTAATACTCTTC | 25879 |
rs184263293 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431243 | ATCAGAGCTAATAAT[A/G]CAACTTAAGCTAACT | 25879 |
rs184289597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428380 | TGTTCTCTTGCGTAC[A/G]TATTGTCTGTAGCTG | 25879 |
rs184297141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423516 | AGAAATGGAGTAAAA[C/T]GGTCATTACTAGGGG | 25879 |
rs184477465 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423079 | TTTCACTAGAGGGGT[A/G]CAGATAAGCTGCCTG | 25879 |
rs184598025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439925 | TCTTACTAGATAGTA[A/G]GTTCTCTGAGAGCAG | 25879 |
rs184783228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426831 | AATGTTCTTAAAGGG[A/T]TAGGGGAATGGGGTA | 25879 |
rs184846509 | snp | A/G | 0.00043805 | 0.014793 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441447 | GATACCAAAATGTGT[A/G]TTTTCAGCTTACATC | 25879 |
rs184905456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437681 | TGTTTCTGTGGTTTG[A/T]TTCCTATCATTATAA | 25879 |
rs185151388 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412821 | TTGGTTTAATAGCAC[A/G]TGCATTCAGAATTAA | 25879 |
rs185242164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434337 | ATGTGGAACTTTGTT[G/T]ATTTAAAGGTTTTCC | 25879 |
rs185258266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430853 | ATGTTCTTTCAGCTC[A/C]CTATTGCTTTTTAGA | 25879 |
rs185281713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427641 | GAAGAAGGAGCATTG[A/G]ACATCATTTTGTCTA | 25879 |
rs185414214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433806 | CATTAACTAGCAATA[A/C]CAAACCACAGTAATT | 25879 |
rs185521818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415756 | TGGGAAACAGTTGTC[G/T]ATAGTGGAGAAAAAT | 25879 |
rs185637511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436507 | TTCTAATATTTAAGA[C/T]TTTTATTGTGTTTTG | 25879 |
rs185763960 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418858 | TATATATATATATAT[A/T]TATATATATTTTTTT | 25879 |
rs185773140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420074 | TGTTTTGCAAGATGT[A/G]TGCATCCCATGATTT | 25879 |
rs185916745 | snp | A/G | 0.00102569 | 0.0226229 | missense | DCAF13 | GRCh38.p7 | 8:103426105 | TGGATGGGCCAGGCT[A/G]TGGAGACGAGGAAGA | 25879 |
rs185973540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419800 | TGGATCACGAGGTCA[C/T]GAGATCGAGACCAGC | 25879 |
rs186048757 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437371 | TGAAACGAGAACAAA[G/T]AAAAAAACAGGACTG | 25879 |
rs186466132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430103 | ACATTAAAATACATG[C/T]ATGGGGGCCAGGTGC | 25879 |
rs186478405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428951 | GAACTTAGTGGTAAA[A/G]GTAAATGGTGTGTGT | 25879 |
rs186572903 | snp | A/G | 1.72276e-05 | 0.00293487 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415117 | AGTACTGAGGGGGCA[A/G]GAACGGGGCACAGAC | 25879 |
rs186623337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424542 | ATGAGATGTTCTAGC[C/T]AGGCACATATTCTTG | 25879 |
rs186794702 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426466 | ATGCTTCAGCTTGTC[G/T]AGTTGATGTCATCAT | 25879 |
rs186810014 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433070 | CTGCTTTTGTGCTAT[A/C]ATGCCTGAGTTGAAT | 25879 |
rs186966417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429583 | TTACTTAATGCCAAG[A/G]GGTTATGTGAGTACC | 25879 |
rs187073630 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435856 | GGATGCATTCTGAGA[A/T]ATGAGTCATTGGGCG | 25879 |
rs187124624 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438307 | TTTTAATAGGACGTT[C/T]TTTTTAATCATCCCC | 25879 |
rs187210651 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427384 | TGTCAGTTTTCCCGA[C/T]TGTAAATGAGTTCTG | 25879 |
rs187260078 | snp | G/T | 0.000824459 | 0.0202867 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427058 | TGCAGATTTGAATTA[G/T]TAATGAAAAAAATCC | 25879 |
rs187330014 | snp | C/T | 0.000134544 | 0.00820085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421289 | GATTAAACTAATATT[C/T]AATTTACCACAAAAG | 25879 |
rs187502529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422564 | TACAAAGAATAATGA[A/G]AAATGAAGACTGAGG | 25879 |
rs187654634 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439304 | CTCTATTAAATTATT[A/C]TTACCTCAACTTATC | 25879 |
rs187662062 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421445 | TGTGGCAAGATATCC[A/G]GAACGTAAAATTTAC | 25879 |
rs187682465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430435 | AAGCATGAGGATTTT[A/G]CAGTGAAAATACTTG | 25879 |
rs187754989 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439731 | AAATGAAGGGGAAAA[A/C]AAGTGTGTTGACCTG | 25879 |
rs188048267 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417010 | ACTGAAAATTAAATA[C/T]ATTAAATAAACGTGG | 25879 |
rs188143359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431319 | CATTGTAAGTAAAAG[C/G]GTATAAAGTTTATTT | 25879 |
rs188153458 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413195 | TGATATGCTTCAAAG[A/C]ACTGTCTAAACTCAT | 25879 |
rs188267905 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417363 | AAAAAGATCTTTGGC[A/T]GGGCGTGGTGGCTTA | 25879 |
rs188304178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428695 | AATTCAAGATGGTGA[C/T]GGTATTACGTACTAA | 25879 |
rs188424107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430945 | CAGTACATTTTAGGC[C/T]TCTAATTAATACTTA | 25879 |
rs188510724 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437443 | GGCTGAATTATTCCA[A/G]AGCTAGTGTGGACAG | 25879 |
rs188530801 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419988 | CACTCCAGCCTGGTG[A/G]CGGAGCAAGACTCCG | 25879 |
rs188558596 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435357 | TTCAAGGTAATTTTT[A/G]TACTCTACTTTTTTT | 25879 |
rs188703144 | snp | A/C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412956 | ATAAATTTTTATTTC[A/C/G]TTATTCATCTTCTTA | 25879 |
rs188962321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440733 | CATACTTTAAAAAAG[A/G]TTCCATGAAAAAATA | 25879 |
rs188970912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423747 | ATTCCACAGTGTCTA[C/T]GTGTATCAAAACACA | 25879 |
rs189207325 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436449 | ATACTCAGCTGTCCC[A/G/T]TAGTCTCGTGTGTGT | 25879 |
rs189240611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423177 | TTACACTTGGTTATT[C/T]TCTTGGATATATTGA | 25879 |
rs189501239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418195 | TCAAGTAGGGATGAT[A/G]TTAAAGTAGCCCAAG | 25879 |
rs189732345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424549 | GTTCTAGCCAGGCAC[A/G]TATTCTTGTTCGGCT | 25879 |
rs189779932 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430368 | CTGCACTCCAGCCTG[C/G]GTGACAGAGCAAGAC | 25879 |
rs189841409 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419141 | CGTCCGTCCCGGCCC[C/G]CCAAAGTGCTGGGAT | 25879 |
rs189843794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427772 | CTGAATTGTGATTCC[C/T]AGTTCCTCCAGGCCT | 25879 |
rs189973361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441808 | TTTGAGACGGAGTCT[C/T]GCTCTGGAGTGCAGT | 25879 |
rs190216894 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434049 | CACCTGAAACAAAGA[G/T]CATATCCCTTATAAT | 25879 |
rs190239900 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416143 | TAAAGAGAATAACAG[A/G]AGCAAAGGTCTTCAG | 25879 |
rs190373384 | snp | A/G | 8.84979e-05 | 0.0066514 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440110 | ACCAAAATCCAAAGG[A/G]TTTTAACTTAATTCG | 25879 |
rs190381842 | snp | C/G | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414663 | TCTAGTTCAGGTTAG[C/G]CAACGCGGACAGCAA | 25879 |
rs190623196 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432185 | AGGTCCCTGAGTGGC[A/G]AAACATCCTACAGTG | 25879 |
rs190716851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426183 | AGCTTGCCTATTAAC[A/G]TTCTTTTATTTAAAA | 25879 |
rs190718906 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443795 | ATCATCTCTAGATTA[C/T]TTATAATACCTAATA | 25879 |
rs190775894 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436833 | ATCCAAATAAATGGA[A/G]ATAATTTTTCTCAAA | 25879 |
rs190873075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437989 | TAGAACTTTTGGTGA[A/G]CTTAATAAACTTAGC | 25879 |
rs190983966 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442336 | TCTTAAGTAAAAAGT[G/T]TTCTGATATACTTTA | 25879 |
rs191010729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425874 | TAGTTTTATGTACTT[C/T]ATGTATTTGTCACAA | 25879 |
rs191120492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420589 | CTCAAGACTAAATTT[C/T]GTTAGGAATACTGTT | 25879 |
rs191161763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429268 | GGTTGAGGGACCTCA[C/G]TAGGGAAGTCTCAGA | 25879 |
rs191295719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426412 | CAATGAAACATTTCC[C/T]ATGGGAAGACCACGG | 25879 |
rs191382460 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429761 | TCATACAGATATTTT[A/C]AATGACACTTTTAAA | 25879 |
rs191588294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433647 | TACCAACTAAAAGCA[A/T]CTTTTATGACTTTCT | 25879 |
rs191643070 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439433 | TCACTCTGTCACCCA[C/T]GCTGGAGTACAGTGG | 25879 |
rs191649200 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421972 | AAAGTCTTTTTAAAC[A/G]AGGGGAACGACAAAA | 25879 |
rs191929265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435904 | ACATCATCAGAGTGC[A/C]CTTAAACAAAACTAG | 25879 |
rs191930302 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417160 | AAATCACATCTGTTA[A/C]CCACGAAACTTTGCA | 25879 |
rs191951704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418020 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 25879 |
rs192135526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434728 | ATTGCTGTATTACTT[C/T]TGTCCATTGTTCATG | 25879 |
rs192223922 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417416 | GGAGGCCGAGACGGG[C/T]GGATCACGAGGTCAG | 25879 |
rs192259757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439920 | ATTTCTCTTACTAGA[C/T]AGTAAGTTCTCTGAG | 25879 |
rs192330983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426632 | GTTTAGTTTTAGCAT[A/G]AGAATAATTTAGAAC | 25879 |
rs192406185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439083 | CACGATCTCGGCTCA[C/T]TGCAAGCTCCGCCTC | 25879 |
rs192540060 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413054 | TCCTGGATCTTTAAT[G/T]TAGGCCTCCAATCCA | 25879 |
rs192666145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440124 | GGTTTTAACTTAATT[C/T]GTTTTCTATAGGGAG | 25879 |
rs192689593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423364 | CACGCACACAGGAAT[A/G]CTATTCAGCCTTCAG | 25879 |
rs192741966 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422595 | AAAACATTTTAGAAA[C/T]GTAGAGATGTAAAAA | 25879 |
rs192825533 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431226 | AATTTCAGGACTTAC[A/G/T]TATCAGAGCTAATAA | 25879 |
rs193004282 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418850 | TATATATATATATAT[A/T]TATATATATATATAT | 25879 |
rs193079494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427420 | TTTGCTCAAATCCCA[A/G]CATGTTTCCCAGCAG | 25879 |
rs193149806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430829 | TTAGAACTCTACATG[A/G]TGATAGTCATGTTCT | 25879 |
rs199561693 | snp | C/T | 0.00299545 | 0.0385844 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426043 | ATCATCATAATAAAA[C/T]AAATATTTCTAGGTT | 25879 |
rs199708023 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103421059 | GGAATATGTACTCGC[C/T]TTTGTGGGACTTCTT | 25879 |
rs199708512 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430380 | CTGGGTGACAGAGCA[A/G]GACTCTGTCTCTAAA | 25879 |
rs199710346 | snp | G/T | 0.00126926 | 0.0251599 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432757 | GTAAGTTTCCCTCTT[G/T]TAAAAACTTGTGTAT | 25879 |
rs199877106 | snp | C/T | 0.000122152 | 0.00781417 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415028 | GACGGTCGCCCCTTG[C/T]GAGCGCAACCCCACC | 25879 |
rs199976025 | snp | C/T | 5.01207e-05 | 0.00500578 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415284 | CGTTTGCCGGCAAAA[C/T]TACGGAGCGGCGCAG | 25879 |
rs199979128 | snp | G/T | 3.35076e-05 | 0.004093 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415325 | AGCCAGCAGGCCGCC[G/T]CTCCGCGAGTCACGT | 25879 |
rs200098745 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423865 | ATTCACCACTTATTT[A/C]CCCCCACTTTATTTT | 25879 |
rs200149472 | snp | G/T | 0.000320337 | 0.0126517 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440281 | GGTGTGGTAAGAGAA[G/T]TCATTTTCTTTCATT | 25879 |
rs200175003 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103426138 | CATTACATACAATAT[C/T]AGGAAAGGTACAAAA | 25879 |
rs200196313 | snp | G/T | 1.66382e-05 | 0.00288424 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415353 | CGTGACTGGAAGTAG[G/T]CTGGGAAAAGCGGAA | 25879 |
rs200232163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441926 | ACGCGCCACCATGCG[C/T]GGCTAATTTTTTGTA | 25879 |
rs200255028 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441781 | GGCCTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTG | 25879 |
rs200340920 | snp | C/T | 0.000383266 | 0.0138379 | missense | DCAF13 | GRCh38.p7 | 8:103432720 | AAGCTTTCATTTTTA[C/T]AGCAGCAAATGAAGA | 25879 |
rs200381394 | snp | C/G/T | 6.65661e-05 | 0.00576882 | missense, synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415413 | GGAACTCCTAGCGGA[C/G/T]ACCTCGTGGAGTCCG | 25879 |
rs200382789 | snp | C/T | 3.31669e-05 | 0.00407215 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420367 | ATTTGCAAAACCATT[C/T]CTTGCTTCGCTGGAT | 25879 |
rs200493628 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442583 | GTTTTTAAACTTAGT[-/A]AAAGGACCCTATTAG | 25879 |
rs200528280 | snp | A/G | 1.65034e-05 | 0.00287253 | missense | DCAF13 | GRCh38.p7 | 8:103440208 | CAGCAAGTATATTAT[A/G]TGTGGATCTGATGAA | 25879 |
rs200624174 | snp | A/C | 0.00949541 | 0.0682462 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421308 | TTACCACAAAAGTGG[A/C]ATTAATGAGAGGTAA | 25879 |
rs200681027 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430383 | GGTGACAGAGCAAGA[C/T]TCTGTCTCTAAATAA | 25879 |
rs200843951 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423862 | CATATTCACCACTTA[-/T]TTCCCCCCACTTTAT | 25879 |
rs200934169 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428707 | TGACGGTATTACGTA[A/C]TAAAAAAAAAACACA | 25879 |
rs200948784 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419990 | CTCCAGCCTGGTGAC[A/G]GAGCAAGACTCCGTC | 25879 |
rs200980273 | snp | C/T | | | stop-gained | DCAF13 | GRCh38.p7 | 8:103430669 | CTGTACGATATGAGG[C/T]AAGCTACTCCTTTGA | 25879 |
rs200987601 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417661 | AAAAAAAAAAAAAAA[C/T]AACATCTTTAATTAC | 25879 |
rs201072797 | snp | A/G | 0.000498753 | 0.0157838 | stop-gained, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415389 | CTGTGGGAGGAGGTG[A/G]CGGTGGGCGGAACTC | 25879 |
rs201079016 | snp | C/G | 8.375e-05 | 0.00647055 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426018 | TAATTTATAACTGTT[C/G]TTCCTTACCATCATC | 25879 |
rs201091409 | in-del | -/AA | 0.0209421 | 0.100162 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424977 | ATCGACATCCTCAAC[-/AA]AAGACATCGCTGTGT | 25879 |
rs201140690 | snp | G/T | 6.78438e-05 | 0.00582385 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415160 | CGGCGGAAAGCGCGA[G/T]GGAGGGGAGGTCCCA | 25879 |
rs201171043 | in-del | -/A | 0.0748431 | 0.178382 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418127 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAGAAAA | 25879 |
rs201279500 | snp | C/T | 0.00399204 | 0.0444982 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421326 | TAATGAGAGGTAAGT[C/T]TAGAAAGAGTTTGGC | 25879 |
rs201585324 | snp | A/G | | | missense | DCAF13 | GRCh38.p7 | 8:103421065 | TGTACTCGCTTTTGT[A/G]GGACTTCTTTTTTCA | 25879 |
rs201666891 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428271 | ACACTTTCTAGAGAC[A/G]CTACAGGTCTAGAAT | 25879 |
rs201707246 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103420450 | CTGTCCTTTCTGGGG[C/T]GTGTGATGGAGAGGC | 25879 |
rs201710496 | snp | C/G/T | 9.98709e-05 | 0.00706587 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415416 | ACTCCTAGCGGACAC[C/G/T]TCGTGGAGTCCGGCC | 25879 |
rs201743683 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428721 | ACTAAAAAAAAAACA[G/T]AAAAAAACCTAAACA | 25879 |
rs201771178 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103430652 | CTGACAGGAATATAG[C/T]ACTGTACGATATGAG | 25879 |
rs201906277 | snp | C/T | 0.00199795 | 0.0315433 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414765 | GAGGATGCAGCCCGG[C/T]GTCTGGGCGGGCTCT | 25879 |
rs201914563 | snp | C/T | 3.30246e-05 | 0.0040634 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103427198 | AACTAATCCTATATG[C/T]TCAATGACCTGGGGA | 25879 |
rs201933283 | snp | A/T | 0.000133556 | 0.00817069 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415335 | CCGCCGCTCCGCGAG[A/T]CACGTGACTGGAAGT | 25879 |
rs201949129 | snp | A/C/T | 6.60125e-05 | 0.00574478 | synonymous-codon, stop-gained | DCAF13 | GRCh38.p7 | 8:103435759 | TTCGATAAATCTATT[A/C/T]GAATCTTTCCTGTAG | 25879 |
rs201969417 | snp | A/C/T | 3.32581e-05 | 0.00407776 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415373 | GAAAAGCGGAAGTCG[A/C/T]CTGTGGGAGGAGGTG | 25879 |
rs202185627 | snp | A/C/G | 5.21158e-05 | 0.00510447 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440132 | CTTAATTCGTTTTCT[A/C/G]TAGGGAGGTATATCA | 25879 |
rs202190823 | snp | C/T | 0.00199792 | 0.0315431 | missense | DCAF13 | GRCh38.p7 | 8:103441606 | GCATCATGAAAGAAG[C/T]TCGTCGACGAAAGTA | 25879 |
rs202211338 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414676 | AGCCAACGCGGACAG[-/CA]ACGCTCCCTTCAACG | 25879 |
rs367600025 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413571 | AAATGAGATAATGCA[C/T]CTAAAGCATAGTTCA | 25879 |
rs367610017 | in-del | -/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414680 | AACGCGGACAGCAAC[-/G]CTCCCTTCAACGCTC | 25879 |
rs367722339 | snp | A/G | 0.000116106 | 0.00761838 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426118 | CTATGGAGACGAGGA[A/G]GAGCCATTACATACA | 25879 |
rs367750135 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427853 | TTTAGGAATGGAGGC[C/T]GTCCTGAAGGCTAAG | 25879 |
rs367753667 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418190 | CCAAATCAAGTAGGG[A/G]TGATATTAAAGTAGC | 25879 |
rs367759273 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440070 | TATCCTGATACTTAA[C/T]AGGCAGTGGTTACTC | 25879 |
rs367940278 | in-del | -/CCC | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414682 | GCGGACAGCAACGCT[-/CCC]CCCTTCAACGCTCCT | 25879 |
rs367984414 | in-del | -/AT | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416282 | GGAGATATTATCAAC[-/AT]GTGTGTGAGCATTGC | 25879 |
rs367988802 | snp | A/G | 8.29332e-05 | 0.00643892 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435837 | ATATGTCACTTAACA[A/G]TGGGGATGCATTCTG | 25879 |
rs368174627 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417427 | CGGGCGGATCACGAG[A/G]TCAGGAGATTGAGAC | 25879 |
rs368195456 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427258 | CCCAATTGAGGTAAT[A/G]TTTTTTTTTAAGTAT | 25879 |
rs368337039 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422209 | CAGCAAGTTTTGAAG[G/T]GTGGCAATGGGAAGG | 25879 |
rs368359478 | snp | C/T | 1.6914e-05 | 0.00290805 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415184 | GGTCCCAGCCTCTCC[C/T]GAGTCTCCGCCCTGC | 25879 |
rs368394292 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432578 | TTTACACATAATAGG[C/T]GTTTATGAAATATTT | 25879 |
rs368488034 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415765 | GTTGTCTATAGTGGA[G/T]AAAAATTCCAGCTGC | 25879 |
rs368573028 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422790 | TAAAAAACAGGTTGA[A/G]CTGAGTTATAAAATG | 25879 |
rs368972577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431745 | GTACTAGTTTAATGA[A/G]TAGTCATTTCTGCCC | 25879 |
rs369006861 | snp | A/C/G | 5.12723e-05 | 0.005063 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414752 | GGGCTGACAGTGAGA[A/C/G]GATGCAGCCCGGTGT | 25879 |
rs369209800 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425843 | TGTTTTTCTTTTGCT[C/G]TACTCATTATATTTT | 25879 |
rs369354703 | snp | C/T | 3.30131e-05 | 0.00406269 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441478 | ACGAGAAAAAGCAGC[C/T]AAGGATTATAACCAG | 25879 |
rs369364519 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420002 | GACGGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 25879 |
rs369388757 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423179 | ACACTTGGTTATTCT[A/C]TTGGATATATTGATT | 25879 |
rs369512477 | snp | C/G | 1.6574e-05 | 0.00287867 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430726 | TGCTTTATACAGTTG[C/G]CATTATATATTTCTC | 25879 |
rs369547425 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414278 | TTTCGATTCTAGCTA[C/T]TTTTTCACAGAAACT | 25879 |
rs369578505 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | DCAF13 | GRCh38.p7 | 8:103441566 | CATCTACCAAAATCT[A/G]TCTATAGCCAGATTC | 25879 |
rs369607684 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438249 | TTCAAAAGCAGAGCA[C/T]TGAGCGGGAGAAGAA | 25879 |
rs369791895 | snp | A/G | 1.69407e-05 | 0.00291034 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414820 | GGTCGAGCGGATGCA[A/G]CGCAAGGTTGGATAA | 25879 |
rs369798614 | snp | A/C/G | 1.67458e-05 | 0.00289355 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415457 | CCGAGATGAAGGTGA[A/C/G]GATGCTGAGCCGGAA | 25879 |
rs369823237 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424718 | GAGGGATAGCGTCTT[C/G]AGGAACGGGGTGCTC | 25879 |
rs369863697 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432252 | ATGCCAACAGTGTTC[C/G]CATTGAGAAACACTG | 25879 |
rs369969475 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438794 | GCCTGTTTCCTTCCT[C/G]TTTATATACTCTGCA | 25879 |
rs369969812 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430118 | CATGGGGGCCAGGTG[A/C/T]GGTGGCTCATGCCTG | 25879 |
rs370092079 | in-del | -/ATATATATATATATATA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418850 | TATATATATATATAT[-/ATATATATATATATATA]TTTTTTTTTTTTTTT | 25879 |
rs370109528 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415652 | TTCGCTAAGGCAAAC[A/T]TTGTGCTTACGGAGT | 25879 |
rs370170605 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420679 | ACAGTAAATTAAATA[A/G]TCATGTTTATAATTA | 25879 |
rs370260727 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436770 | TACACATTCCCATTG[G/T]TCCTTAGTAATGCTT | 25879 |
rs370284625 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439277 | ATTACAGGTGTGAGC[C/T]ACCGCACCTGGCTCT | 25879 |
rs370320899 | snp | C/T | 0.000153988 | 0.00877327 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415000 | GACGCGATGCAGTGG[C/T]CGCCACCGTGGCGAC | 25879 |
rs370463972 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438982 | CAAATAGGTATGATA[A/T]TTGACATCTCCATTT | 25879 |
rs370523537 | snp | A/G | 1.69456e-05 | 0.00291075 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415138 | GGGCACAGACACTAC[A/G]TCACGCCGGCGGAAA | 25879 |
rs370589281 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427517 | AAATCCAAGTAAATA[C/T]AGTCTTGTTTTAACT | 25879 |
rs370795277 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431466 | AATCATTTTTATAAC[A/G]TAACAACTAGATATT | 25879 |
rs370878481 | snp | A/G | 2.84669e-05 | 0.00377262 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414940 | CCTGGCCCGTCATAG[A/G]CTCGGGGCCCGTCGA | 25879 |
rs370881916 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439666 | GGCATTAGATTCAGC[A/G]TATCAGGAGGTACTC | 25879 |
rs370936504 | in-del | -/AG | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419070 | TTTTGTATTTTTAGT[-/AG]AGATGGGATTTCACT | 25879 |
rs370976960 | snp | C/T | 3.34476e-05 | 0.00408934 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415256 | GCACAGCTAAAGAAC[C/T]GCCCCTTGCTAACGT | 25879 |
rs371140183 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419985 | CTGCACTCCAGCCTG[A/G]TGACGGAGCAAGACT | 25879 |
rs371142059 | snp | A/G | 0.000116018 | 0.00761548 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435836 | CATATGTCACTTAAC[A/G]ATGGGGATGCATTCT | 25879 |
rs371185840 | snp | A/T | 0.000110088 | 0.00741834 | missense | DCAF13 | GRCh38.p7 | 8:103442829 | CACAGCAAGCCTGGA[A/T]CTGTGCCACTTGTGT | 25879 |
rs371332126 | snp | C/T | 0.00130568 | 0.0255173 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421117 | GTCATTAAATTTGAT[C/T]AACATAGGTAAGAAT | 25879 |
rs371486662 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418671 | ACATAAGAATGACCT[A/G]GGCTAGAGCTTTGTT | 25879 |
rs371495072 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428290 | CAGGTCTAGAATAGG[C/T]TGGCAAACTAGTCTG | 25879 |
rs371569836 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417138 | TTTAAGAGGTTTACA[C/G]TGATTGAAATCACAT | 25879 |
rs371574862 | snp | C/G | 0.000272013 | 0.011659 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426169 | GTAAATTGACTAATA[C/G]CTTGCCTATTAACAT | 25879 |
rs371786632 | snp | A/G | 1.68949e-05 | 0.0029064 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415193 | CTCTCCCGAGTCTCC[A/G]CCCTGCCTCGCCCAC | 25879 |
rs371813265 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436197 | GATTATTATTTATCT[C/T]TTCTGAGAGGGTACC | 25879 |
rs371829345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423271 | TTTGCAGCATTATTC[A/G]CAATACCCAGGATAT | 25879 |
rs371856361 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428718 | ACGGTATTACGTACT[-/A]AAAAAAAAAACACAA | 25879 |
rs371962144 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429382 | GAATTGCGTACAGAC[A/C]GTAGGAGGAGTTAGC | 25879 |
rs372003121 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417370 | TCTTTGGCTGGGCGT[A/G]GTGGCTTATGCCTGT | 25879 |
rs372084361 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440284 | GTGGTAAGAGAATTC[A/G]TTTTCTTTCATTGTC | 25879 |
rs372145169 | snp | C/T | 1.71749e-05 | 0.00293038 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420225 | AGACTGCAGGAAATA[C/T]TAAGTGTGAATTATT | 25879 |
rs372192553 | in-del | -/TAATGAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422558 | AACTACTACAAAGAA[-/TAATGAA]AAATGAAGACTGAGG | 25879 |
rs372261811 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439035 | TTTTTTGAGATGGAG[G/T]CTTGCTCTGTTGCCC | 25879 |
rs372397168 | snp | C/T | 0.000336086 | 0.0129588 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427280 | TTTAAGTATGTTTTA[C/T]TTATTATGGCTTAAT | 25879 |
rs372455118 | snp | C/T | 0.000117856 | 0.00767555 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420926 | TGAATTTATCCTGAA[C/T]ATTTTACATTTATAG | 25879 |
rs372466428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431838 | TGCCTCCTGCTTTGC[A/G]CATTCTCAGTTTTTA | 25879 |
rs372518680 | snp | A/G | 8.23811e-05 | 0.00641746 | missense | DCAF13 | GRCh38.p7 | 8:103421012 | AGCGGAATTGTATCC[A/G]TACAATACAAGCACA | 25879 |
rs372650826 | snp | A/C | 0.000153988 | 0.00877328 | stop-gained, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415137 | GGGGCACAGACACTA[A/C]GTCACGCCGGCGGAA | 25879 |
rs372661597 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423710 | GTGAGGTAACAGATA[C/T]GTTAATTAGCTTGGT | 25879 |
rs372714335 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103432687 | TGAGAACAAATACAA[C/T]CTGTTGGAACCCTAT | 25879 |
rs372885817 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436117 | TAATGGACCACTGTC[A/G]TATATGCAGTCTCTC | 25879 |
rs372902714 | snp | A/G | 3.73741e-05 | 0.00432269 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414965 | CGTCGACACCACGGC[A/G]CCCAGGGCCGCGGAG | 25879 |
rs372912555 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442167 | TATGTTTAAAGGACA[A/G]ACGATGAAAATGAGT | 25879 |
rs372990650 | snp | A/G/T | 1.84664e-05 | 0.00303856 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442837 | GCCTGGATCTGTGCC[A/G/T]CTTGTGTCAGAGAAG | 25879 |
rs373059297 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433836 | GAAGCTTTTTTTTTT[-/T]AACCTTTATTGATGT | 25879 |
rs373149310 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439124 | GCCATTCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 25879 |
rs373378051 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | DCAF13 | GRCh38.p7 | 8:103421021 | GTATCCGTACAATAC[A/T]AGCACATGAAGGCTT | 25879 |
rs373403840 | snp | C/T | 3.30322e-05 | 0.00406387 | missense | DCAF13 | GRCh38.p7 | 8:103420282 | CAAGAAACTATGATC[C/T]TGCTTTACATCCTTT | 25879 |
rs373477118 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437991 | GAACTTTTGGTGAGC[G/T]TAATAAACTTAGCAT | 25879 |
rs373525321 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417125 | CCAGTCCCACTCTTT[-/T]AAGAGGTTTACAGTG | 25879 |
rs373671098 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434509 | AGTTGTCAATGTCTT[A/G]CTACTAGTAATGTTA | 25879 |
rs373721597 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432414 | TTTTAACTTTTATTA[C/T]GTGTCACATTTTTCT | 25879 |
rs373758134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430001 | GAAGTATTACTTATA[A/G]TAGTAAAAAACAGGA | 25879 |
rs373804376 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417066 | GTATGCTTTCTTTGT[C/G]AAGTACAGGCATTCT | 25879 |
rs373812057 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423189 | ATTCTCTTGGATATA[C/T]TGATTAATAGCTCAG | 25879 |
rs373812134 | snp | A/G | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103441486 | AAGCAGCCAAGGATT[A/G]TAACCAGAAATTGAA | 25879 |
rs373908312 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421759 | TTTACTTAACATAAT[C/T]GTCTTCAAGGTTTAT | 25879 |
rs373956646 | snp | G/T | 1.72609e-05 | 0.00293771 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414836 | CGCAAGGTTGGATAA[G/T]ACGCCGCCGCTCACG | 25879 |
rs373965340 | in-del | -/A | 0.36315 | 0.222928 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420007 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 25879 |
rs374072300 | snp | C/T | 3.66113e-05 | 0.00427835 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435620 | TATTTAAAAATTCTT[C/T]TACAGCTTATATACT | 25879 |
rs374095345 | snp | A/C | 5.57802e-05 | 0.00528081 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442758 | CTTTAAGATGAGTTC[A/C]CATAACTTGCTTATA | 25879 |
rs374177027 | snp | A/G | 0.000116321 | 0.0076254 | missense | DCAF13 | GRCh38.p7 | 8:103440165 | CAAAGAGAATGCAAC[A/G]TGTTATCTGTGTAAA | 25879 |
rs374192461 | snp | C/G/T | 0.000152546 | 0.00873227 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415140 | GCACAGACACTACGT[C/G/T]ACGCCGGCGGAAAGC | 25879 |
rs374257876 | snp | C/T | 1.81237e-05 | 0.00301023 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415066 | CCAACGAGAGGACTC[C/T]TATGCCCAAGGCGCG | 25879 |
rs374259569 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419427 | CGCCTGGCACTTGAA[C/T]TCTTATGTGAGTCTT | 25879 |
rs374265201 | snp | A/G | 0.000153988 | 0.00877328 | missense | DCAF13 | GRCh38.p7 | 8:103441573 | CAAAATCTATCTATA[A/G]CCAGATTCAGGAACA | 25879 |
rs374268334 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439675 | TTCAGCATATCAGGA[A/G]GTACTCTTTGAAGAC | 25879 |
rs374270704 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417284 | ATTAAAACCAAACAT[C/T]GAATTAAGCTGAAAT | 25879 |
rs374390026 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | DCAF13 | GRCh38.p7 | 8:103421057 | GAGGAATATGTACTC[A/G]CTTTTGTGGGACTTC | 25879 |
rs374464432 | snp | A/G | 3.39288e-05 | 0.00411865 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415166 | AAAGCGCGATGGAGG[A/G]GAGGTCCCAGCCTCT | 25879 |
rs374540163 | snp | A/G | 1.80377e-05 | 0.00300308 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415511 | CCAAGTTGGACTTAC[A/G]GAGAGGTAAGATAAG | 25879 |
rs374554896 | snp | C/T | 0.000123267 | 0.00784972 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420506 | AACTAAAAGTAGTTA[C/T]ATTACAAATGTTTTC | 25879 |
rs374564048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415686 | TGCGGAACTGGATGG[A/G]TAGCAAGTAAAGTCT | 25879 |
rs374654375 | snp | A/G | 3.29772e-05 | 0.00406048 | missense | DCAF13 | GRCh38.p7 | 8:103430661 | ATATAGTACTGTACG[A/G]TATGAGGCAAGCTAC | 25879 |
rs374721908 | snp | A/G | 6.62712e-05 | 0.00575597 | missense | DCAF13 | GRCh38.p7 | 8:103426113 | CCAGGCTATGGAGAC[A/G]AGGAAGAGCCATTAC | 25879 |
rs374751047 | snp | A/G | 1.66244e-05 | 0.00288304 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427087 | CCTCTTAACCTTTTT[A/G]CTTTTAAAGACAGTG | 25879 |
rs374878048 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431130 | TATTTGTTCAGTTAC[A/G]TGCTGATCAATACTA | 25879 |
rs374880797 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437373 | AAACGAGAACAAAGA[A/G]AAAAACAGGACTGTG | 25879 |
rs374957899 | snp | A/C/G | 0.000133308 | 0.00816326 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415428 | CACCTCGTGGAGTCC[A/C/G]GCCGGAAGAGCAACC | 25879 |
rs374959896 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436267 | AAAATTAGTAATAAT[A/G]CTTTACATTTGTTAT | 25879 |
rs375018347 | snp | C/T | 1.65701e-05 | 0.00287833 | stop-gained | DCAF13 | GRCh38.p7 | 8:103441464 | TTTCAGCTTACATCA[C/T]GAGAAAAAGCAGCCA | 25879 |
rs375223755 | snp | C/G | 6.59914e-05 | 0.00574381 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103430620 | TTTTTAGACATTTCT[C/G]TTGGGAAGTTGTGCA | 25879 |
rs375397922 | snp | A/G | 6.84568e-05 | 0.0058501 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420233 | GGAAATATTAAGTGT[A/G]AATTATTAAGAAGGA | 25879 |
rs375406944 | snp | A/G | 8.67822e-05 | 0.00658662 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441416 | TACTGAAGCAAAACA[A/G]CACACTATTCATTAA | 25879 |
rs375511038 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429607 | GAGTACCATGCACAT[G/T]TATAATTGACTTACA | 25879 |
rs375532699 | snp | A/T | 3.3423e-05 | 0.00408783 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415268 | AACCGCCCCTTGCTA[A/T]CGTTTGCCGGCAAAA | 25879 |
rs375651914 | snp | C/T | 0.000697094 | 0.0186564 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426174 | TTGACTAATAGCTTG[C/T]CTATTAACATTCTTT | 25879 |
rs375740775 | snp | C/T | 0.000116286 | 0.00762426 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420955 | AGTTCACTGAAATTT[C/T]CTGGTATGCCTTATC | 25879 |
rs375767025 | in-del | -/AGGAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432623 | GGAAAAGAAAAGGAA[-/AGGAA]GTGGGAAATTCATCC | 25879 |
rs375768638 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424221 | TTTAGTAGAGACAGG[A/G]TTTCACCGTGTTAGC | 25879 |
rs375771006 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416206 | CTGTGTCATTAGTTT[-/G]AATGAGGAGTAAGCG | 25879 |
rs376213810 | snp | C/T | 2.09045e-05 | 0.00323293 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442861 | AGAGAAGAAGAAACA[C/T]GTAGTGGCAGTTGTA | 25879 |
rs376293859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425184 | AGATTGCATCTAATA[C/T]ATAAATGTAAGATTT | 25879 |
rs376483947 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436007 | GTTCAGCATGTTACT[A/G]TGCTGAATACTGTGG | 25879 |
rs376533222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423319 | TCCAGCAATGGATGA[A/G]TGAATTTTAAAAAAA | 25879 |
rs376534034 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421141 | TAAGAATAATCTAAT[G/T]GAATACATTTTTTTT | 25879 |
rs376551963 | snp | A/C/G | 1.68926e-05 | 0.0029062 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414803 | GAAGCGGATCTTCAC[A/C/G]AGGTCGAGCGGATGC | 25879 |
rs376638763 | snp | C/T | 0.000313105 | 0.0125082 | missense | DCAF13 | GRCh38.p7 | 8:103421056 | CGAGGAATATGTACT[C/T]GCTTTTGTGGGACTT | 25879 |
rs376762690 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422443 | GTAGCCTTGGGGAAT[A/G]CCCACCTCTGGGAAG | 25879 |
rs376828600 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433398 | GATATTAAAGCGGGG[A/G]GATTAGTCTCCCAGG | 25879 |
rs376889407 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440300 | TTTTCTTTCATTGTC[A/C]TAAAGCTGATTTCTA | 25879 |
rs376970883 | snp | G/T | 1.6477e-05 | 0.00287024 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441523 | ATTTCAGCATTATCC[G/T]CATATAAAACGTATA | 25879 |
rs377166611 | snp | C/T | 0.000155988 | 0.00883005 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414992 | GGAGGTGGGACGCGA[C/T]GCAGTGGCCGCCACC | 25879 |
rs377242970 | snp | A/C | | | missense | DCAF13 | GRCh38.p7 | 8:103441507 | AGAAATTGAAGGAGA[A/C]ATTTCAGCATTATCC | 25879 |
rs377292603 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436119 | ATGGACCACTGTCGT[A/G]TATGCAGTCTCTCAT | 25879 |
rs377599158 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427266 | AGGTAATGTTTTTTT[C/T]TAAGTATGTTTTACT | 25879 |
rs377603904 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438359 | TAATGGTTTATCAAA[A/G]TGCTTAAAACATACC | 25879 |
rs377660638 | snp | A/G/T | 8.2752e-05 | 0.00643189 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435824 | GCCATTTATATTCAT[A/G/T]TGTCACTTAACAATG | 25879 |
rs377666609 | snp | C/T | 2.75319e-05 | 0.00371015 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414937 | GGCCCTGGCCCGTCA[C/T]AGGCTCGGGGCCCGT | 25879 |
rs377669779 | in-del | -/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417661 | AAAAAAAAAAAAAAA[-/G]AACATCTTTAATTAC | 25879 |
rs377699657 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438075 | GGGGAGGATTCTCAG[C/T]TACTTAAGTGACTAA | 25879 |
rs377711032 | snp | C/T | 1.66535e-05 | 0.00288556 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421104 | ATAATACCATTAAGT[C/T]ATTAAATTTGATCAA | 25879 |
rs386728404 | in-del | ACGCT/CCC | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414678 | CCAACGCGGACAGCA[ACGCT/CCC]CCCTTCAACGCTCCT | 25879 |
rs386728405 | multinucleotide-polymorphism | ATT/TTC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417594 | TTGCAGTGAGCCGAG[ATT/TTC]GCGTCACTGCACTCC | 25879 |
rs398112815 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417352 | TTTCTTAAAAAAAAA[-/A]GATCTTTGGCTGGGC | 25879 |
rs527281758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425735 | TGAATGACTAACCAG[A/C]TATTATAATACCATT | 25879 |
rs527284553 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439165 | GCCTGCCACCATGCC[G/T]GGCTAATTTTTTGCA | 25879 |
rs527319190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418366 | CTCTACAAAAAATTT[A/G]AAGATTAATGGGGCA | 25879 |
rs527348434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419106 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 25879 |
rs527355367 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415758 | GGAAACAGTTGTCTA[C/T]AGTGGAGAAAAATTC | 25879 |
rs527894719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431104 | TTAGAACTCATTCAC[A/G]TAACCAGCTTTATTT | 25879 |
rs527933029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431786 | ACCTAACACTCATTC[G/T]GTTTTTTTTTTAATT | 25879 |
rs528150201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437583 | ATCACAGTCTTAATA[A/T]GTGTTAACGTCCTGT | 25879 |
rs528390536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417518 | GTGGTGCTGGGTGCC[C/T]GTAGTCACAGCTACT | 25879 |
rs528496237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428963 | AAAAGTAAATGGTGT[A/G]TGTGTCTCTTATCCT | 25879 |
rs528516455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421593 | AAACAATAACTCCTC[C/T]GTCCCCTCAGTCCCC | 25879 |
rs528535728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422346 | TGACATCATCAATAT[A/G]GAACTAATCATTGAA | 25879 |
rs528572838 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429843 | GTAGTGTATACTGGT[A/G]CAGCTCTTTGGAAAA | 25879 |
rs528802236 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420894 | CCCAGTAGAGTGATT[C/T]GTAGCCTTGTCAGTG | 25879 |
rs528889896 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414658 | TCAAATCTAGTTCAG[G/T]TTAGCCAACGCGGAC | 25879 |
rs529075604 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435431 | TGTGTTGGTATATAT[A/G]TAAGTGGAGTCTTAA | 25879 |
rs529411296 | snp | A/G | 3.42114e-05 | 0.00413576 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432621 | GGGGAAAAGAAAAGG[A/G]AAGGAAGTGGGAAAT | 25879 |
rs529447697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426253 | TGCAGATAAGAAACG[A/G]AAGACTTTAGGCTGT | 25879 |
rs529452982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441212 | CGTGGCCCTACTCCT[A/T]CAGCACTGCTGCTTT | 25879 |
rs529491755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433223 | AATGGAAATGAAAAT[A/G]TCTGCCTGCAATGTT | 25879 |
rs529549509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419770 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCGTGT | 25879 |
rs529678919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424785 | AATGTCTCTTTGGGT[C/G]AAGCCAGATCAGTCA | 25879 |
rs529699648 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424360 | AATGTGTGCTTTGTC[A/C/G]GAGATAAGACACATG | 25879 |
rs529755479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425727 | AATTTTTTTGAATGA[C/G]TAACCAGATATTATA | 25879 |
rs529772323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417636 | GACAGAGGGAGACTC[C/T]GTCTCAAAAAAAAAA | 25879 |
rs529986122 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413088 | TCAATCCTTTTATCT[C/G]TCACCTCAGCCCCAC | 25879 |
rs530036571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416320 | GTCTCTGCTCAAAAG[A/G]TGTTTACAGTTTGTC | 25879 |
rs530072781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416971 | TAGACTTCAAAAATA[A/G]TCTTTGCAAAACTGA | 25879 |
rs530369200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438482 | CTAGAGTGCAGTGAT[A/G]CCACACGGCTCACTA | 25879 |
rs530483566 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443007 | GTAGAGCTTTATTGT[C/T]ACTCCTTTTAGCTAC | 25879 |
rs530716668 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426869 | GAGGTAGAGATAATT[C/T]GTAGTTGGAAACACG | 25879 |
rs530870033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428375 | AGCCATGTTCTCTTG[C/T]GTACATATTGTCTGT | 25879 |
rs530920047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434297 | AGGTGAGGGTTAGAA[C/T]AGATGATCCCTAATG | 25879 |
rs530958180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427816 | GAGATTGGCCACTAC[A/G]TGTCGTCTGTTTAGG | 25879 |
rs531125360 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414713 | CCTCCCCCTAGAACG[G/T]AAAAGACGGAGGAGA | 25879 |
rs531201032 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433597 | AAGTAGTAGTGTTAG[C/T]TCATAAAAGGATTTA | 25879 |
rs531203653 | snp | A/G | 3.40292e-05 | 0.00412474 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415481 | GCCGGAATCCGGACA[A/G]TTATGTCCGCGAAAC | 25879 |
rs531241871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419731 | CATATAAAAGGGAGG[C/T]CGGGCACGGTGGCTC | 25879 |
rs531346082 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428708 | ACGGTATTACGTACT[-/A]AAAAAAAAAACACAA | 25879 |
rs531409145 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414012 | TGTAGCCCATACAGC[A/T]GTCTACAAATATTAA | 25879 |
rs531440991 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435884 | GCGATTTCATCATTG[G/T]GTGAACATCATCAGA | 25879 |
rs531541022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441988 | GCCAAGATGGTCTCA[A/G]TCTCCTGACCTCGTG | 25879 |
rs531553593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433450 | TTTTTTTCCCAAAGC[A/G]TTTATTATAGCGCTA | 25879 |
rs531567041 | in-del | -/C/T | 0.00584488 | 0.0537427 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427258 | CCAATTGAGGTAATG[-/C/T]TTTTTTTTTAAGTAT | 25879 |
rs531956301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432577 | CTTTACACATAATAG[G/T]TGTTTATGAAATATT | 25879 |
rs532169574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430374 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACTCTGTC | 25879 |
rs532197452 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442016 | GTGATCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 25879 |
rs532207348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424058 | AAGTCTCCCTCTGTC[A/G]CCCAGGTTGGAGTGC | 25879 |
rs532299262 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425669 | TTTTTTACATTTAAA[A/G]TTACCTGGAATTTTA | 25879 |
rs532661259 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418614 | AAAGAGATGATGAGT[A/G]GGACTTTGAGTTTTG | 25879 |
rs532847033 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416386 | TTGTCACTTGGATTT[A/G]GCATCGTTCCCAGTC | 25879 |
rs532878557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437071 | GGAGTGTTCTGATGA[A/C]TTTGATCTTCATTTC | 25879 |
rs533096761 | snp | C/T | 3.69276e-05 | 0.00429679 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442816 | GAATCGTATTAAACA[C/T]AGCAAGCCTGGATCT | 25879 |
rs533136660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435083 | GGGAATTTAATAAGC[A/G]TTATATATAATAAAA | 25879 |
rs533271672 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423674 | GTGAATTAAATGTTC[C/T]CACCACAAAATAATA | 25879 |
rs533290548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439223 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCACCTA | 25879 |
rs533347295 | snp | A/G | 1.74549e-05 | 0.00295417 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441405 | TAGCTTTTTTATACT[A/G]AAGCAAAACAACACA | 25879 |
rs533357601 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422028 | ATTTGACAGCAGTTA[A/G]TGATCAGTTTGAAGG | 25879 |
rs533417669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434210 | AGTTCAAGTCTAGGC[C/T]GACCAGTAATTACTG | 25879 |
rs533556309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427751 | TATTTTTCTTTGCTC[A/C]GAAGTCTGAATTGTG | 25879 |
rs533638821 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414686 | GACAGCAACGCTCCC[C/T]TCAACGCTCCTCCTC | 25879 |
rs534004434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439843 | TTTTATTTGCATTTT[A/G]TGCTTTTAGTTATTC | 25879 |
rs534066527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430073 | TATTACAAATTAGAA[A/C]ACAGTAATATCTGTA | 25879 |
rs534103484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430487 | GATGATTTATTGTAC[C/T]CTCTTAAAATGGACT | 25879 |
rs534120175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432062 | TCCATCTACTAGTCT[A/G]TCAATGTTTCTTTTA | 25879 |
rs534144630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424403 | GCTGGTACAACTTTA[A/C]GAATGTTTTTAAAAA | 25879 |
rs534244962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434353 | ATTTAAAGGTTTTCC[A/G]TGTACACAAATTGAT | 25879 |
rs534375078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422742 | TAATCAGTCAAATAG[A/G]TCTTCCTTATTCTTT | 25879 |
rs534397544 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434557 | AGGGTGGTGTCTGCC[-/A]GGTTTCTCCACTAAA | 25879 |
rs534472047 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419884 | CGTGGTGGCATGCGC[C/T]TGTAATCCCAGCTAC | 25879 |
rs534511323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415880 | ACAGGCTTTTAAAAC[C/T]TTCCTACTGCTCTTC | 25879 |
rs534584968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436207 | TATCTTTTCTGAGAG[G/T]GTACCTGAGTTTAAT | 25879 |
rs534626354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421946 | GTACAAATACCAATT[A/C]AAGTTCATTGAAAGT | 25879 |
rs534849351 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416462 | ACGTTTCCCACAAGT[A/G]GTTTAGTATTCACCC | 25879 |
rs534916686 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443160 | TACTTACTTTCTCTT[A/T]GATCTATTATTGTAG | 25879 |
rs535047258 | snp | A/C | 1.68886e-05 | 0.00290586 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414804 | AAGCGGATCTTCACG[A/C]GGTCGAGCGGATGCA | 25879 |
rs535090434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440656 | ACTCAAAGGCTGCAA[G/T]TCCCTGGGAGATCTT | 25879 |
rs535147722 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441925 | CACGCGCCACCATGC[A/G]CGGCTAATTTTTTGT | 25879 |
rs535190221 | snp | A/G | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103427147 | AGCTGTTTTTGCCAC[A/G]TGTGGACAGCAAGTA | 25879 |
rs535213813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432841 | TAGGTAGGTATACCT[A/G]TAAAGTTTGAAAACT | 25879 |
rs535219601 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441589 | CCAGATTCAGGAACA[A/G]CGCATCATGAAAGAA | 25879 |
rs535251067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433569 | GTTCCACTATGTAGA[C/T]TTGGAAGCAAAAAAG | 25879 |
rs535267018 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416766 | TGCACTGTTAAGACA[G/T]CACCTAGCACATAGT | 25879 |
rs535344893 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427961 | TCAGTAGGGATATGT[G/T]TTTCCTGTTGAAAGA | 25879 |
rs535387876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435419 | TAGGGTGGAAAATGT[A/G]TTGGTATATATATAA | 25879 |
rs535433771 | snp | G/T | 0.000219542 | 0.0104749 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427309 | ATAATTTCAGTTCTG[G/T]TTAGAAAACTTTTGA | 25879 |
rs535680910 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412872 | TAGATTTTAACTTTA[G/T]TAAATGAGTTTAATT | 25879 |
rs535697159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419965 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 25879 |
rs536417403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437178 | CAAATTGTCATGAGT[G/T]TTTTTTTGGCATTAT | 25879 |
rs536565346 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440831 | TGTTTTTCTAAATGT[C/G]CCATATTTTCTATAA | 25879 |
rs536588686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423411 | TCACTTGCAGCATAC[A/G]TGAATGAACCTGGAG | 25879 |
rs536647096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435319 | TTATGCTGTACTAAA[A/T]AACTGGCCTCTGGGT | 25879 |
rs536797299 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | DCAF13 | GRCh38.p7 | 8:103421042 | ATGAAGGCTTTGTAC[A/G]AGGAATATGTACTCG | 25879 |
rs536834190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429475 | ATTGTAGGCAGAAGC[C/T]AATAGTTGTGAGTGT | 25879 |
rs536867587 | snp | A/G | 3.35807e-05 | 0.00409747 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415315 | GATCCAGTTGAGCCA[A/G]CAGGCCGCCGCTCCG | 25879 |
rs537020947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434470 | TAGCTGAAAACCACT[G/T]TTCTTAGGCAGGAAC | 25879 |
rs537070526 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413740 | TTTTCCTTCATAGAA[C/T]GGGTTCTTGCTTCCT | 25879 |
rs537076775 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442170 | GTTTAAAGGACAAAC[A/G]ATGAAAATGAGTTAC | 25879 |
rs537086823 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434765 | CATTTGAAGCACTAT[C/T]CTTTTAGCCATTAGA | 25879 |
rs537243431 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424530 | ACCAGCCTGGAGATG[A/G]GATGTTCTAGCCAGG | 25879 |
rs537466172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419925 | GAGGCAGGAGAATTG[C/T]TTGAACCTGAGAAGC | 25879 |
rs537514630 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414413 | AGCTGCCAAACCACG[C/T]GGGTATGCTAAGATT | 25879 |
rs537816333 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438046 | AAGTTAAGAACTCAG[C/T]ATAGTTTACCATTGG | 25879 |
rs537861370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430756 | CTGTAAATAGAGTGA[C/G]TAACAATATGGAGCA | 25879 |
rs537998487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424486 | AAGATATACCAGTTT[C/G]TAATACCAACAATTC | 25879 |
rs538033618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425038 | CTTATCTGTTTTCAT[C/G]TCATGGGCACTGTAA | 25879 |
rs538074213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417885 | AGCACTTTGGGAGGC[C/T]GAGGCGGGAAGATCA | 25879 |
rs538109457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418610 | TTGCAAAGAGATGAT[A/G]AGTAGGACTTTGAGT | 25879 |
rs538316866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416584 | CACCGAACAGTAATC[C/T]GTTCCTGCTTACCTC | 25879 |
rs538404202 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442221 | TCATATTAAAAAATT[A/G]TTGTAAAAAATGTTT | 25879 |
rs538626413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422913 | ATTTGAAAGATTGTC[A/G]TGTGAAAAAGAAAAT | 25879 |
rs538649863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416006 | TGATGAAAGAATGGT[G/T]AAATGAAATTAATTT | 25879 |
rs538859138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436285 | TTACATTTGTTATTT[C/T]TTACTTAGTCAAATC | 25879 |
rs538942563 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417582 | AGGAGGCAGAGCTTG[C/T]AGTGAGCCGAGATTG | 25879 |
rs539058376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433635 | ATGTTTTAGTGGTAC[C/G]AACTAAAAGCATCTT | 25879 |
rs539143488 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437723 | TCATGCTTGGGTGAA[-/T]TAATCTGTATTTAAA | 25879 |
rs539195948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427311 | AATTTCAGTTCTGTT[A/T]AGAAAACTTTTGAAT | 25879 |
rs539381877 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441685 | TCTCACCAAAAACAA[A/C]GTTAACTGCCATTCA | 25879 |
rs539464303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418796 | GTTTTTTTAGACATA[C/T]GAGCTTAAAATTACT | 25879 |
rs539559313 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424986 | CTCAACAAAAGACAT[C/T]GCTGTGTAATCTTAG | 25879 |
rs539593882 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420700 | TTTATAATTAAAGTA[G/T]TTAAGTATGAGTTTT | 25879 |
rs539634733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420906 | ATTCGTAGCCTTGTC[A/G]GTGTTGAATTTATCC | 25879 |
rs539672574 | snp | A/C | 0.000396405 | 0.0140729 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414835 | GCGCAAGGTTGGATA[A/C]GACGCCGCCGCTCAC | 25879 |
rs539676623 | snp | A/G | 6.62043e-05 | 0.00575307 | missense | DCAF13 | GRCh38.p7 | 8:103427223 | TGGGGATTTGACAGT[A/G]TAAGTAGTGTTAAAT | 25879 |
rs539874239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419206 | TGATTATTAACCAAG[A/G]CAATGTGTTTAGCAG | 25879 |
rs539993673 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438536 | GTGATCCTCCTACCT[C/T]AGACTCCTGAGCAGC | 25879 |
rs540011652 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413664 | TGCATCATAAAACTT[C/T]ATGACATTATATGTC | 25879 |
rs540064704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424610 | CCAGAATTGGTGGTC[C/T]GCTGAGGTTTGTACT | 25879 |
rs540176794 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431401 | CAAGTCTGTTGTCGT[-/A]AGTCCACATACAAAA | 25879 |
rs540197915 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429007 | TGGAAAGGGCATGTT[C/G]CTGTGAACAAATGGA | 25879 |
rs540209550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417530 | GCCTGTAGTCACAGC[C/T]ACTCAGGAGGCTGAG | 25879 |
rs540403941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430844 | ATGATAGTCATGTTC[G/T]TTCAGCTCCCTATTG | 25879 |
rs540410431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423069 | TTCAGTTACTTTTCA[C/G]TAGAGGGGTGCAGAT | 25879 |
rs540577201 | snp | C/T | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441490 | AGCCAAGGATTATAA[C/T]CAGAAATTGAAGGAG | 25879 |
rs540644850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421177 | TCATTTATTTGTTCC[G/T]AGGCCCTTTTGGAGT | 25879 |
rs540793825 | snp | A/G | 0.000135616 | 0.00823345 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415147 | CACTACGTCACGCCG[A/G]CGGAAAGCGCGATGG | 25879 |
rs540964817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435949 | TGCACACCTAGGCTG[C/T]GTGGTCATATGATAT | 25879 |
rs540966558 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443948 | CAGTTGGTTGAGTCT[A/G]TGGGCGAGGAACCCA | 25879 |
rs540989931 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415700 | GATAGCAAGTAAAGT[C/G]TGTTCAAGTCCTTTT | 25879 |
rs541399526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428187 | CTGCAGTGCGATGTG[A/G]GCTTGGCCTTGAGGA | 25879 |
rs541483881 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438147 | TAATGGTTACGGAAA[A/C]CTGATTGAATTTCCC | 25879 |
rs541536722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441350 | GGCAATTTTGGTTGC[A/G]TATCATAAAAGATTA | 25879 |
rs541565187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433234 | AAATATCTGCCTGCA[A/G]TGTTTGTATTGCGGT | 25879 |
rs541677277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419502 | GCTATATAATATCAT[C/G]ATAATCACAACTTCG | 25879 |
rs541802191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416997 | ACTGATGGATGAGAC[A/T]GAAAATTAAATATAT | 25879 |
rs541874650 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425541 | GAGGCCCAAAGTTCA[C/T]AGTTTGAAAACCACT | 25879 |
rs541875357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417999 | CGGGCATGGTGGCGG[A/G]TGCCTGTAGTCCCAG | 25879 |
rs541988304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419067 | AACTTTTTGTATTTT[C/T]AGTAGATGGGATTTC | 25879 |
rs542064475 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413089 | CAATCCTTTTATCTG[A/T]CACCTCAGCCCCACT | 25879 |
rs542101329 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413842 | ACACATGGCCATCAG[C/T]AATGTAGAATTTTCT | 25879 |
rs542151073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439236 | GACCTCGTGATCCAC[A/C]TACTGCAGCCTCCCA | 25879 |
rs542188610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424575 | CGGCTACTCATTTCT[A/G]TAAAATGAGAAAACC | 25879 |
rs542462107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430261 | GCCCGGTGTGGTGGC[A/G]CACCCCTGTAATCCC | 25879 |
rs542552323 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423251 | TTAAAATGAATAAAG[C/G]CTCATTTGCAGCATT | 25879 |
rs542580904 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443799 | TCTCTAGATTACTTA[C/T]AATACCTAATACAAT | 25879 |
rs542662988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435891 | CATCATTGTGTGAAC[A/C]TCATCAGAGTGCACT | 25879 |
rs542778047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436855 | TTTCTCAAAAAATTA[G/T]GATAATTGGATGATC | 25879 |
rs542796064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428901 | GCAGCTGTATTTGTT[C/T]AGCTGTTTTTTTTTT | 25879 |
rs542850604 | snp | A/G | 6.60404e-05 | 0.00574594 | missense | DCAF13 | GRCh38.p7 | 8:103435784 | CTGTAGACAAAAGTC[A/G]AAGCAGGTATGTGCC | 25879 |
rs542950533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430810 | ATCTTTTATACAGGT[G/T]TTCTTAGAACTCTAC | 25879 |
rs542963030 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428810 | AACATCTGTGTCAGA[A/C]GAGCCGATCACCAAT | 25879 |
rs542975296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434807 | TGAATCTTGAAACTC[A/G]TGAAGTCATTGTTTT | 25879 |
rs543006487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418173 | AATAGTGTAAATTGC[C/T]GCCAAATCAAGTAGG | 25879 |
rs543023582 | snp | A/G/T | 1.66568e-05 | 0.00288585 | missense | DCAF13 | GRCh38.p7 | 8:103420380 | TTCCTTGCTTCGCTG[A/G/T]ATGGTCACCGTGATG | 25879 |
rs543092068 | snp | G/T | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443159 | ATACTTACTTTCTCT[G/T]TGATCTATTATTGTA | 25879 |
rs543197401 | snp | C/T | 4.32236e-05 | 0.00464865 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415037 | CCCTTGTGAGCGCAA[C/T]CCCACCTCCGGGACC | 25879 |
rs543215892 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439082 | GCACGATCTCGGCTC[A/G]CTGCAAGCTCCGCCT | 25879 |
rs543504248 | in-del | -/AGAG | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418571 | CAAAAAACTAGAAAT[-/AGAG]AGTTGAAAGATGAGT | 25879 |
rs543793688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433701 | AGTTTGAGGTTACAG[A/T]GAGTTGTAATTGGGC | 25879 |
rs543816545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438463 | TCTGGCTCTGTCAGC[C/T]AGGCTAGAGTGCAGT | 25879 |
rs544001080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441139 | CAAAATTTGAGTGAG[C/T]GATTTAGGTGCTTTT | 25879 |
rs544172340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430152 | TCCCAGCACTTTGGG[A/G]GGCTGAGGCAGGTGG | 25879 |
rs544206966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423735 | CTTGGTTTATCCATT[C/T]CACAGTGTCTACGTG | 25879 |
rs544424804 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416943 | GCTGACATCAGAGTA[C/G]ATAGAAATTTTCTAG | 25879 |
rs544428139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425956 | GAATGATATGGTATG[A/T]TACCTGTTTTAAACA | 25879 |
rs544562746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418947 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 25879 |
rs544686138 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439070 | TGGAGTGCAGTAGCA[C/G]GATCTCGGCTCACTG | 25879 |
rs544746374 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425848 | TTCTTTTGCTCTACT[C/T]ATTATATTTTTAGTT | 25879 |
rs544934974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429667 | GTTGGACAAAAGACA[C/G]GCCTAATTTATAGAG | 25879 |
rs544966601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436831 | AAATCCAAATAAATG[A/G]AAATAATTTTTCTCA | 25879 |
rs545013136 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437372 | GAAACGAGAACAAAG[A/T]AAAAAACAGGACTGT | 25879 |
rs545027113 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433993 | TTTTCAGAGTGTCCT[C/T]GGAATTTCTCATTCC | 25879 |
rs545365914 | snp | A/T | 1.75764e-05 | 0.00296444 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426162 | TACAAAAGTAAATTG[A/T]CTAATAGCTTGCCTA | 25879 |
rs545431666 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432050 | TTGCTTCTTTGCTCC[A/G]TCTACTAGTCTATCA | 25879 |
rs545481090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434245 | AACTTGGGCAAGTCA[C/T]TTAAACTAACTCTAT | 25879 |
rs545528987 | in-del | -/GAT | 0.0080296 | 0.0628516 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420479 | GCAAGTGTCAATCTA[-/GAT]GATATTTTCAACTAA | 25879 |
rs545591190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428233 | GAGGACACTCTTCCT[C/G]CAACTACCACATGCT | 25879 |
rs545627987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428845 | AAATCGTAATTATTA[A/G]GGATGACCTAGTGAC | 25879 |
rs545762886 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422173 | CCTGGGAAGAGGTTG[G/T]TTCCTGTTGCTGAGG | 25879 |
rs545964980 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413993 | GAACTTTATTAGATA[C/G]TTCTGTAGCCCATAC | 25879 |
rs546205765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440775 | CATTGGCTGGTTACC[C/T]CCAGGATAGGGGATT | 25879 |
rs546450622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416494 | TGCAAATCTCAGTGC[C/G]TTTCAGTCATCTTTT | 25879 |
rs546557436 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419868 | AGAAAAATTAGCTGG[C/G]CGTGGTGGCATGCGC | 25879 |
rs546570906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436927 | ACTTGTGATATTTAA[A/G]TCTTTTTCCACTGTA | 25879 |
rs546600701 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422043 | GTGATCAGTTTGAAG[C/G]CCATTTTAATAGTTT | 25879 |
rs546695543 | in-del | -/G | 0.00143693 | 0.0267657 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427258 | CCCAATTGAGGTAAT[-/G]TTTTTTTTTAAGTAT | 25879 |
rs546715856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429921 | GATTCAGTAATGTCA[C/T]TTGTGAAATTTTATC | 25879 |
rs546748455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423989 | AGGCATGAGTCACCA[C/T]GCCCACCTTATTGTT | 25879 |
rs546754035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430364 | ACCACTGCACTCCAG[A/C]CTGGGTGACAGAGCA | 25879 |
rs546939539 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413200 | TGCTTCAAAGCACTG[C/T]CTAAACTCATCAGGC | 25879 |
rs547188696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442060 | TGAGCCACCATGCCC[C/T]GCCCAGAAGGCCATT | 25879 |
rs547289245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434878 | CCCTTTGAAAGGCCA[C/T]GTTCACTCTTACATA | 25879 |
rs547324001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428657 | TGATAACATATGTGA[A/G]CATTTTTTAAAAGTG | 25879 |
rs547412747 | in-del | -/TAAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430412 | AAATAAATAAATAAA[-/TAAA]ATACAAGCATGAGGA | 25879 |
rs547520208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442746 | TGAGAAAGTTTTCTT[C/T]AAGATGAGTTCCCAT | 25879 |
rs547637799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426877 | GATAATTTGTAGTTG[A/G]AAACACGTTAGTAAT | 25879 |
rs547676639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419793 | AGGCGTGTGGATCAC[A/G]AGGTCACGAGATCGA | 25879 |
rs547704768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420780 | TTTTGTAACACTTTA[C/G]AATCAACAGAGTATT | 25879 |
rs547911503 | in-del | -/TAAA | 0.0023933 | 0.0345097 | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443823 | ATACAATGTAAATGC[-/TAAA]TAAATAGTTGTTATA | 25879 |
rs548062124 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424057 | GAAGTCTCCCTCTGT[C/T]GCCCAGGTTGGAGTG | 25879 |
rs548133874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424788 | GTCTCTTTGGGTCAA[A/G]CCAGATCAGTCAAGA | 25879 |
rs548207633 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417658 | AAAAAAAAAAAAAAA[A/G]AAGAACATCTTTAAT | 25879 |
rs548323228 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431251 | TAATAATACAACTTA[A/G]GCTAACTCTCAAGAG | 25879 |
rs548335809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437893 | GCAAACAAGTAAATT[A/G]ATAGTGTTCACATGG | 25879 |
rs548344102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418241 | ACCCAAACTGCCTGG[A/G]AATGCAGTGGCTCAC | 25879 |
rs548471894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438488 | TGCAGTGATGCCACA[C/T]GGCTCACTACAGCCC | 25879 |
rs548626855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424307 | GCTGGGATTACAGGC[A/G]CGAGCCGCCATGCCC | 25879 |
rs548751419 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420918 | GTCAGTGTTGAATTT[A/G]TCCTGAACATTTTAC | 25879 |
rs548832847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429261 | CAAGAAAGGTTGAGG[A/G]ACCTCACTAGGGAAG | 25879 |
rs548869557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422701 | TTTTGACCTACCTAT[A/G]CAACAGTTTTTGTAT | 25879 |
rs548889760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431048 | AAATTCAAGCCCCAT[G/T]ATTATCGTATGACAT | 25879 |
rs548930423 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430340 | GAGGTTGCAGTGAGC[C/T]AAGATTGCACCACTG | 25879 |
rs549009416 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426593 | TGTTTCTACCAAATT[A/G]TTCTGCAAATCAGGT | 25879 |
rs549096971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436092 | GTACAGTAAAAATCC[A/G]GTATTATCTTAATGG | 25879 |
rs549127353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429768 | GATATTTTAAATGAC[A/G]CTTTTAAATGACACT | 25879 |
rs549157534 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442352 | TTCTGATATACTTTA[A/T]TATAACATGACATCT | 25879 |
rs549209028 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430843 | GATGATAGTCATGTT[C/G]TTTCAGCTCCCTATT | 25879 |
rs549541582 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414723 | GAACGGAAAAGACGG[A/C]GGAGATCCAGTTCGG | 25879 |
rs549578358 | snp | C/G/T | 0.000270592 | 0.0116287 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415183 | AGGTCCCAGCCTCTC[C/G/T]CGAGTCTCCGCCCTG | 25879 |
rs549660993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442001 | CAATCTCCTGACCTC[A/G]TGATCGCCTGCCTCG | 25879 |
rs549960663 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413108 | TCAGCCCCACTAGTC[-/T]TCCTAATACTCTTCC | 25879 |
rs549966244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418612 | GCAAAGAGATGATGA[A/G]TAGGACTTTGAGTTT | 25879 |
rs550040038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433461 | AAGCATTTATTATAG[C/T]GCTATGCCTTTGATA | 25879 |
rs550078607 | snp | A/C | 5.00822e-05 | 0.00500386 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427080 | AAAAAATCCTCTTAA[A/C]CTTTTTGCTTTTAAA | 25879 |
rs550102585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419149 | CCGGCCCCCCAAAGT[G/T]CTGGGATTACAGGCG | 25879 |
rs550313855 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428468 | AACCTAAAATACTTA[-/CT]CTCTGGCCCTTTACA | 25879 |
rs550429040 | snp | A/G | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441556 | TCGTCATCGACATCT[A/G]CCAAAATCTATCTAT | 25879 |
rs550536713 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431076 | CATGTACACTATTTT[A/T]TTCCAGAAGGTTTTA | 25879 |
rs550552428 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423904 | GACAGAGTCTTGCTA[C/T]GTTGCCCAGGCCGAT | 25879 |
rs550582251 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428855 | TATTAGGGATGACCT[A/G]GTGACCATGTTTTTC | 25879 |
rs550691298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424106 | TCACTGCAAGCTCTG[C/T]CTCCCGGGTTCACGC | 25879 |
rs550727474 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424700 | ACTATCAGAAACTTG[A/T]TGGAGGGATAGCGTC | 25879 |
rs550766627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417605 | CGAGATTGCGTCACT[A/G]CACTCCAGCCTGGGT | 25879 |
rs550985823 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437131 | TGTTCCTATGTGACT[A/G]TTGCTTCCTTTGTTG | 25879 |
rs551022319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429977 | CTACGTGGGGGGGAA[A/G]TGTTTATTGAAGTAT | 25879 |
rs551117209 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428704 | TGGTGACGGTATTAC[A/G]TACTAAAAAAAAAAC | 25879 |
rs551274577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437719 | ATAACTCATGCTTGG[A/G]TGAATAATCTGTATT | 25879 |
rs551297230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422474 | TGGGAAAACTCTAGG[A/G]GTAGCCAGAGCTCAA | 25879 |
rs551368575 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433625 | TTATTATATGATGTT[G/T]TAGTGGTACCAACTA | 25879 |
rs551407796 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436227 | CTGAGTTTAATAAAG[G/T]TTTTTGCTCCAATAC | 25879 |
rs551445591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433387 | CCCCTTTTTAAGATA[C/T]TAAAGCGGGGAGATT | 25879 |
rs551509281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435965 | GTGGTCATATGATAT[A/G]GCCTGTTGCTTCTAG | 25879 |
rs551694914 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414688 | CAGCAACGCTCCCTT[C/G]AACGCTCCTCCTCCC | 25879 |
rs551883533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419892 | CATGCGCCTGTAATC[C/T]CAGCTACTCGGGTGG | 25879 |
rs551900792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426934 | TAAAATGTCTTGTCT[C/T]ATTATGGTATTGTTT | 25879 |
rs551973994 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426574 | CATGTATAAATCTTA[C/T]TAATGTTTCTACCAA | 25879 |
rs551978406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420545 | TTTTAGTTACTGTAG[G/T]TTTTACTTTATTGGA | 25879 |
rs552034466 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413161 | TTCTCAGGTACCAAG[A/G]ATTCCCTTTCCTCAG | 25879 |
rs552427511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440355 | AAATTTACTTTTAGG[C/T]ATTTTTGGGTATTTT | 25879 |
rs552448418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431788 | CTAACACTCATTCTG[G/T]TTTTTTTTTAATTTA | 25879 |
rs552487085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425781 | TTTCTCCAAGTTGAA[A/G]TGCCATGTTTATCAC | 25879 |
rs552654829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438674 | TACTGGGATTATAGG[C/T]ATGAGCCACTGCACC | 25879 |
rs552655539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422009 | CTGTGCTTTGAGTTA[A/C]GTAATTTGACAGCAG | 25879 |
rs552792650 | snp | C/T | 1.66938e-05 | 0.00288905 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415336 | CGCCGCTCCGCGAGT[C/T]ACGTGACTGGAAGTA | 25879 |
rs552820635 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418631 | GACTTTGAGTTTTGG[C/T]AGTAGGGAATATGGA | 25879 |
rs552853053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436551 | TTTACTACATATTAT[A/T]TGTTATTAAATACAG | 25879 |
rs553474664 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433578 | TGTAGATTTGGAAGC[A/C]AAAAAGTAGTAGTGT | 25879 |
rs553570484 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443170 | CTCTTTGATCTATTA[C/T]TGTAGACACTATACA | 25879 |
rs553616382 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439093 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 25879 |
rs553648361 | snp | A/G | 0.000399281 | 0.0141238 | missense | DCAF13 | GRCh38.p7 | 8:103427211 | TGTTCAATGACCTGG[A/G]GATTTGACAGTATAA | 25879 |
rs553686751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428193 | TGCGATGTGAGCTTG[A/G]CCTTGAGGAATTACT | 25879 |
rs553725567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428833 | TCACCAATTCTAAAA[G/T]CGTAATTATTAGGGA | 25879 |
rs553951296 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431320 | ATTGTAAGTAAAAGG[G/T]TATAAAGTTTATTTC | 25879 |
rs554001116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418764 | GTAAGAAGATGCATT[C/T]ACTTTTTACTCACTG | 25879 |
rs554098469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425206 | GTAAGATTTTAAGTT[A/T]AAACTAGCAGTTTTG | 25879 |
rs554099260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438197 | TGCTTTGGAAAAAAG[A/G]GCTTCTTAGGTATGT | 25879 |
rs554144090 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414491 | CTTAAAATGTGACAA[G/T]CCCTTCTTTATTTTA | 25879 |
rs554237834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418001 | GGCATGGTGGCGGGT[C/G]CCTGTAGTCCCAGCT | 25879 |
rs554308926 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422460 | CCACCTCTGGGAAGT[C/G]GGAAAACTCTAGGAG | 25879 |
rs554801772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441179 | TGATGCCTAGGGAAG[A/G]TCCAACTCAGTGATC | 25879 |
rs555016227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428180 | TGAGATGCTGCAGTG[C/T]GATGTGAGCTTGGCC | 25879 |
rs555063477 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433584 | TTTGGAAGCAAAAAA[-/G]TAGTAGTGTTAGCTC | 25879 |
rs555069499 | snp | A/G | 3.68243e-05 | 0.00429078 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415060 | CCGGGACCAACGAGA[A/G]GACTCTTATGCCCAA | 25879 |
rs555079466 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416769 | ACTGTTAAGACAGCA[C/G]CTAGCACATAGTTGC | 25879 |