SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs555097127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430010 | CTTATAATAGTAAAA[A/G]ACAGGAAACAAGTCT | 25879 |
rs555330515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416652 | TGATTCTATCACTTC[C/T]TCACAGTGTTTATCA | 25879 |
rs555430302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428766 | CTATTTAGAGGAACA[A/G]AAAAATCTTTTGCTT | 25879 |
rs555766980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419941 | TTGAACCTGAGAAGC[A/G]GAGGTTGCAGTGAGC | 25879 |
rs555799060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434486 | TTCTTAGGCAGGAAC[C/T]GTAAAGCAGTTGTCA | 25879 |
rs555803984 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414416 | TGCCAAACCACGTGG[A/G]TATGCTAAGATTTCA | 25879 |
rs555808958 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436367 | ATTGTCAAGACCGTT[C/T]TCCCTCTATTTCACT | 25879 |
rs556001306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433764 | CCCTGGTGTCTTAAA[A/G]AAATAAAAGAAGCTC | 25879 |
rs556021573 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425699 | ATTTTCACATAAGGC[A/G]TCAAATTGGCTCAAT | 25879 |
rs556037583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432803 | CTTAATTGTATAAGT[C/T]GTACTAATAAAATAT | 25879 |
rs556045071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441859 | CAAGCTCCGCCTCCC[G/T]GGTTCATGCCATTCT | 25879 |
rs556217173 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440924 | TATTTTCTACTTAGT[C/T]CTGATAGGAAAATCA | 25879 |
rs556239307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432253 | TGCCAACAGTGTTCC[C/T]ATTGAGAAACACTGA | 25879 |
rs556250801 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437337 | TTTTTCCAACATGGT[A/G]CATAAGTAGACAAAA | 25879 |
rs556267025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425050 | CATCTCATGGGCACT[A/G]TAAACTGTTTTGCAA | 25879 |
rs556307609 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417916 | CGAGGTCAGGAGATC[A/G]AGACTATCCTGGCTA | 25879 |
rs556374589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431264 | TAAGCTAACTCTCAA[G/T]AGGGAGACAGATACT | 25879 |
rs556418925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442190 | AAATGAGTTACCAAA[A/G]TAAGAAAACACTTGC | 25879 |
rs556474447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430760 | AAATAGAGTGACTAA[A/C]AATATGGAGCAAATA | 25879 |
rs556526732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419413 | GGTTTTTGGAACAGC[A/G]CCTGGCACTTGAACT | 25879 |
rs556649236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416039 | CCTTCCTGGTCTGTT[A/C]CCCCGTTAACATGCT | 25879 |
rs556963567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423353 | GTACACACACACACG[C/G]ACACAGGAATACTAT | 25879 |
rs556999835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416596 | ATCTGTTCCTGCTTA[A/C]CTCCTGCATGAGCCC | 25879 |
rs557018503 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422923 | TTGTCATGTGAAAAA[C/G]AAAATAGACTAATTT | 25879 |
rs557159455 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443452 | TCCTTTCAGCATTGA[A/G]ACTTTGGCCTATTTT | 25879 |
rs557243896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438058 | CAGCATAGTTTACCA[C/T]TGGGGAGGATTCTCA | 25879 |
rs557333280 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417377 | CTGGGCGTGGTGGCT[A/T]ATGCCTGTAATCCCA | 25879 |
rs557544178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428883 | TTCAAACTTGCCTGT[A/G]TAGCAGCTGTATTTG | 25879 |
rs557599125 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435999 | ACGAATCTGTTCAGC[A/C]TGTTACTGTGCTGAA | 25879 |
rs557625751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429418 | ATGCAACTATTTAGT[A/G]AATAGCTCTTCTTGC | 25879 |
rs557717946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422939 | AAAATAGACTAATTT[A/G]TTGCTCCATAGAGAG | 25879 |
rs558002866 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413673 | AAACTTCATGACATT[A/G]TATGTCTTTGTGGTG | 25879 |
rs558065658 | snp | A/G | 0.000551383 | 0.0165948 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415294 | CAAAACTACGGAGCG[A/G]CGCAGGATCCAGTTG | 25879 |
rs558092062 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418797 | TTTTTTTAGACATAC[A/G]AGCTTAAAATTACTT | 25879 |
rs558109329 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413590 | AAGCATAGTTCACTG[C/T]CTTGCTCCTAGTAAA | 25879 |
rs558143540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426321 | AAGTCCTTTGATGCT[A/G]AAGAATTTTAACAGT | 25879 |
rs558185911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441789 | CTTTTTTCTTTTTTT[G/T]TTTTTTGAGACGGAG | 25879 |
rs558406526 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419672 | AAGTGTATTGGAAGC[C/T]CTGACAGTGAACACT | 25879 |
rs558412848 | snp | A/C | 0.000805964 | 0.0200582 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440851 | ATTTTCTATAAGAAA[A/C]AGAGTGTTTATATTA | 25879 |
rs558464661 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427572 | TCATGTTCCATAGAT[G/T]ATGTCATTGTACATT | 25879 |
rs558514029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439901 | GCTTAGTTTGTTCAT[A/G]TTTATTTCTCTTACT | 25879 |
rs558648982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430501 | CCCTCTTAAAATGGA[C/T]TTTGTTTTTTAACAT | 25879 |
rs558684081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424443 | ACAGTGTTGCAAAAC[A/G]TAAACTTTTATTACC | 25879 |
rs558804989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423661 | AATTGCTATGAAAGT[A/G]AATTAAATGTTCTCA | 25879 |
rs558830796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431535 | TGATAATCTTTCCAA[A/G]GTACCACTTATATGA | 25879 |
rs558910482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425936 | GATCAATAAGTGTAA[C/T]ACTGGAATGATATGG | 25879 |
rs558951765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437398 | ACTGTGTAGTTACCT[A/G]TGATCCCAAGGGGCC | 25879 |
rs559098779 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423876 | TTTCCCCCCACTTTA[-/T]TTTTTTTAAAGAGAC | 25879 |
rs559128672 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437779 | AAATGGCTAAAGCAT[A/G]TTATTTTTAAAATAA | 25879 |
rs559154380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434883 | TGAAAGGCCATGTTC[A/T]CTCTTACATATCACC | 25879 |
rs559189507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435957 | TAGGCTGTGTGGTCA[C/T]ATGATATGGCCTGTT | 25879 |
rs559198818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417247 | AGTGAGTACTGCTTG[A/C]ATTTTTTTTATAATA | 25879 |
rs559230597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429010 | AAAGGGCATGTTGCT[A/G]TGAACAAATGGAGTG | 25879 |
rs559258406 | snp | A/G | 3.4506e-05 | 0.00415353 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415114 | TCTAGTACTGAGGGG[A/G]CAAGAACGGGGCACA | 25879 |
rs559764141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432434 | CACATTTTTCTGACT[A/G]AACTGTAAGTTGTTT | 25879 |
rs559765214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441924 | GCACGCGCCACCATG[C/T]GCGGCTAATTTTTTG | 25879 |
rs559856124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433247 | CAATGTTTGTATTGC[A/G]GTGAGTATCAGGTAG | 25879 |
rs559895379 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434090 | TGGAGTATCATAATT[A/C/G]CTCTTTGAAAATGAT | 25879 |
rs560034611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427715 | ATTATTGTTGAACTG[C/T]ATGGTAATTAGTTAT | 25879 |
rs560080523 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420779 | GTTTTGTAACACTTT[A/G]GAATCAACAGAGTAT | 25879 |
rs560117900 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418926 | TCACACTCTGTCAGC[C/T]AGGCTGGAGTGCAGT | 25879 |
rs560179982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418348 | TCATAAGGAGACCCC[C/T]GTCTCTACAAAAAAT | 25879 |
rs560207054 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427824 | CCACTACATGTCGTC[C/T]GTTTAGGTCTGAATT | 25879 |
rs560406776 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432874 | CATCTGTTTAGCTTT[-/AA]AAAGTTTTCCAAATT | 25879 |
rs560856474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419166 | TGGGATTACAGGCGT[G/T]AGCCACCACGCCCGG | 25879 |
rs560959426 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103441533 | TATCCTCATATAAAA[C/T]GTATAGCTCGTCATC | 25879 |
rs561050905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424577 | GCTACTCATTTCTAT[A/T]AAATGAGAAAACCCT | 25879 |
rs561184656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430298 | TCCACAGGCTGAGGC[A/G]TGAGAATTGCTTGAA | 25879 |
rs561221008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423916 | CTACGTTGCCCAGGC[C/T]GATGTTGAACTCCTG | 25879 |
rs561299228 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414060 | GAACTGAATTGCCTA[A/C]TGCTAAAATAAACAA | 25879 |
rs561382315 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439239 | CTCGTGATCCACCTA[C/G]TGCAGCCTCCCAAAG | 25879 |
rs561427641 | snp | C/T | 1.99575e-05 | 0.00315885 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415552 | GAAAGGGACGGTTTC[C/T]GCAAGTCGTTGGGTC | 25879 |
rs561438030 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414650 | CCATTTCCTCAAATC[G/T]AGTTCAGGTTAGCCA | 25879 |
rs561457224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422342 | AACTTGACATCATCA[A/G]TATAGAACTAATCAT | 25879 |
rs561574559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442047 | GGGATTACAGGTGTG[A/C]GCCACCATGCCCCGC | 25879 |
rs561613359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442673 | TTACCTATTGTCATC[A/G]TGAAAATATTTTTTT | 25879 |
rs561659844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434828 | TCATTGTTTTTACCA[A/G]TTGTGCATAAAGTAT | 25879 |
rs561979185 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426837 | CTTAAAGGGATAGGG[G/T]AATGGGGTATGAGTA | 25879 |
rs562050704 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442355 | GATATACTTTATTAT[-/A]AACATGACATCTATC | 25879 |
rs562059424 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419746 | CCGGGCACGGTGGCT[C/G]ATGCCTGTAATCCCA | 25879 |
rs562417892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427494 | GTGTGCATTTGCCCA[C/T]TGGGGTAAAATCCAA | 25879 |
rs562420365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431617 | TAGACTTTTAAGCAC[A/G]TTAACCTAAAATGTG | 25879 |
rs562493127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416310 | TTGCTAATAAGTCTC[C/T]GCTCAAAAGATGTTT | 25879 |
rs562497018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423738 | GGTTTATCCATTCCA[C/T]AGTGTCTACGTGTAT | 25879 |
rs562537384 | in-del | -/TG | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420071 | AATTGTTTTGCAAGA[-/TG]TATGCATCCCATGAT | 25879 |
rs562542176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430901 | TAGGTATTGTATCCT[A/G]GTCACCAACCTTGTG | 25879 |
rs562624115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418174 | ATAGTGTAAATTGCC[A/G]CCAAATCAAGTAGGG | 25879 |
rs562635380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416955 | GTAGATAGAAATTTT[C/T]TAGACTTCAAAAATA | 25879 |
rs562726866 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438362 | TGGTTTATCAAAGTG[C/T]TTAAAACATACCTAT | 25879 |
rs562796763 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413077 | CCAATCCAAACTCAA[C/T]CCTTTTATCTGTCAC | 25879 |
rs563031833 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431903 | TAGCCTGGCTTTCAA[C/G]GTGCTCTGAAATCTG | 25879 |
rs563208305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438480 | GGCTAGAGTGCAGTG[A/G]TGCCACACGGCTCAC | 25879 |
rs563320679 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418193 | AATCAAGTAGGGATG[A/T]TATTAAAGTAGCCCA | 25879 |
rs563451895 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430188 | CTGAGGTCAGGAGTT[A/T]GATACCAGCCTGGGC | 25879 |
rs563466611 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425617 | TTCAATATTATAACA[A/G]TGCCTTCTCTCCAGT | 25879 |
rs563747014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442567 | TTTATTAACTGTGGA[A/G]GGTTTTTAAACTTAG | 25879 |
rs563789152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428351 | GTAAATAGAGCTCTG[C/G]TAGAAGACAGCCATG | 25879 |
rs563829829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419646 | GCTAGGCATAAGGAA[A/G]TACAAATGAAAAGTG | 25879 |
rs563967216 | snp | A/G | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443406 | TTTATAAATAATAAT[A/G]TAATTTGGGTCAAGT | 25879 |
rs564038600 | snp | C/G/T | 3.32835e-05 | 0.00407932 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415409 | GGGCGGAACTCCTAG[C/G/T]GGACACCTCGTGGAG | 25879 |
rs564054619 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414001 | TTAGATACTTCTGTA[A/G]CCCATACAGCAGTCT | 25879 |
rs564548427 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425929 | ATAAATGGATCAATA[A/T]GTGTAATACTGGAAT | 25879 |
rs564593363 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423571 | ATGTTGGTCAAAAGA[C/G]ACAAAATTTCAAATA | 25879 |
rs564818661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432981 | GTGGACCAAATCCTT[C/T]CTGTTGCCTGTTTTT | 25879 |
rs564982937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429584 | TACTTAATGCCAAGG[G/T]GTTATGTGAGTACCA | 25879 |
rs565053568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418030 | CTACTCGGGAGGCTG[A/G]GGCAGGAGAATGGTG | 25879 |
rs565092440 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415640 | TCTCAGTTACCTTTC[G/T]CTAAGGCAAACTTTG | 25879 |
rs565159866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425334 | AAACATGTCTGCCAA[A/G]TACCCATGTCTAAAT | 25879 |
rs565170419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417546 | ACTCAGGAGGCTGAG[A/G]CGGGAGAATGGTGTG | 25879 |
rs565292301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416838 | TTTTGCCTACATGAA[C/G]AGATTTAGAAACAAA | 25879 |
rs565360834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423101 | AGCTGCCTGACCCTG[C/G]AAGCCCAGTGTTGTG | 25879 |
rs565397659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416212 | CATTAGTTTGAATGA[A/G]GAGTAAGCGAGATGA | 25879 |
rs565405441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433618 | AAAGGATTTATTATA[G/T]GATGTTTTAGTGGTA | 25879 |
rs565580613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428019 | ATTTTAGCAGTTATT[A/G]CGAGGCTACCATTTT | 25879 |
rs565608903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428675 | TTTTTTAAAAGTGCT[A/G]TCCAAATTCAAGATG | 25879 |
rs565738140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442061 | GAGCCACCATGCCCC[A/G]CCCAGAAGGCCATTT | 25879 |
rs565788946 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428114 | AGATAGGAAGTAAGG[C/T]TGAGTCAAAATAGTA | 25879 |
rs565816351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420824 | TTTTTGCTCATCAGT[A/G]TACTTATCCATATGC | 25879 |
rs565852534 | snp | A/G | 1.70015e-05 | 0.00291555 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414826 | GCGGATGCAGCGCAA[A/G]GTTGGATAAGACGCC | 25879 |
rs566009485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426286 | TTGTTGACCCATTTA[C/T]GCAATATTTAATGCA | 25879 |
rs566014871 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414286 | CTAGCTATTTTTTCA[C/T]AGAAACTTGTACCAT | 25879 |
rs566073118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432053 | CTTCTTTGCTCCATC[C/T]ACTAGTCTATCAATG | 25879 |
rs566111711 | snp | A/C | 0.000399281 | 0.0141238 | missense | DCAF13 | GRCh38.p7 | 8:103432741 | CAAATGAAGATTATA[A/C]GTAAGTTTCCCTCTT | 25879 |
rs566390713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417717 | TTGAGAAGGGATCTG[C/T]TCAAAAACTCTGTTA | 25879 |
rs566405754 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417122 | GAACCAGTCCCACTC[-/T]TTTAAGAGGTTTACA | 25879 |
rs566530470 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429819 | ATTAAAATGGACATA[G/T]CCCACATTGTAGTGT | 25879 |
rs566543224 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423702 | ATAAGTATGTGAGGT[A/T]ACAGATATGTTAATT | 25879 |
rs566617241 | in-del | -/T | 0.00584488 | 0.0537427 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427259 | CCAATTGAGGTAATG[-/T]TTTTTTTTAAGTATG | 25879 |
rs566714938 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437922 | GGAAAAATTAGTGTG[A/G]CTGTGTATATAAAGA | 25879 |
rs566758015 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430480 | GATTATGGATGATTT[A/T]TTGTACCCTCTTAAA | 25879 |
rs567061068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424859 | GGTTTCTAGAATTGA[A/G]TTTTAGTATAGTGCC | 25879 |
rs567159970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417205 | TTCCAGTATGCAACC[C/T]GTCCCGTTAATACAG | 25879 |
rs567172960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415782 | AAAATTCCAGCTGCT[G/T]CTCTGGGATTGTCTT | 25879 |
rs567327839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429266 | AAGGTTGAGGGACCT[C/T]ACTAGGGAAGTCTCA | 25879 |
rs567366610 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103422721 | AGTTTTTGTATACAC[A/G/T]TGCGCTAATCAGTCA | 25879 |
rs567748395 | snp | A/G | 0.000118228 | 0.00768766 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414795 | TTACCGGCGAAGCGG[A/G]TCTTCACGAGGTCGA | 25879 |
rs567768556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440609 | CAGAACTTAGAGCTC[A/G]TATCTCTTGTTAGAG | 25879 |
rs567912637 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443145 | TTTTTATTACAGATA[C/T]ACTTACTTTCTCTTT | 25879 |
rs567986929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434339 | GTGGAACTTTGTTTA[C/T]TTAAAGGTTTTCCAT | 25879 |
rs567993381 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436737 | GTATAGTGAATTATG[A/G]TTTACAAAGAGCTGT | 25879 |
rs568236562 | snp | A/G | 1.65034e-05 | 0.00287253 | missense | DCAF13 | GRCh38.p7 | 8:103427160 | ACATGTGGACAGCAA[A/G]TAGACATTTGGGATG | 25879 |
rs568313524 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424179 | GCCCACCACCACTCC[C/T]GGCTAATTTTTTTAT | 25879 |
rs568362769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418698 | TGTTGAATGTTAGAT[A/G]TAACACCATTACCAG | 25879 |
rs568421039 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431929 | ATCTGGTTCTAATTT[A/G]CAACTCATTTATTTC | 25879 |
rs568436517 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413420 | GTTCCAGAGTTAGAT[C/T]ACCTGGGTTTAAATC | 25879 |
rs568479247 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431269 | TAACTCTCAAGAGGG[A/G]GACAGATACTGTCTG | 25879 |
rs568493154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439565 | AACTAACTTTTGTAA[C/T]TTTAGTAGAGACAAG | 25879 |
rs568618279 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417194 | TGGGGAATTGATTCC[A/G]GTATGCAACCCGTCC | 25879 |
rs568680947 | in-del | -/AC | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414690 | GCAACGCTCCCTTCA[-/AC]GCTCCTCCTCCCCCT | 25879 |
rs568685875 | snp | C/T | 0.000357983 | 0.013374 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426186 | TTGCCTATTAACATT[C/T]TTTTATTTAAAATTA | 25879 |
rs568910077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424214 | TTTTATTTTTAGTAG[A/T]GACAGGGTTTCACCG | 25879 |
rs568980627 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433571 | TCCACTATGTAGATT[G/T]GGAAGCAAAAAAGTA | 25879 |
rs568989526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417635 | TGACAGAGGGAGACT[A/C]CGTCTCAAAAAAAAA | 25879 |
rs569423711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437759 | TTTTCCTTTAAAAGA[C/T]CTTAAAATGGCTAAA | 25879 |
rs569450316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430412 | AAATAAATAAATAAA[A/T]AAAATACAAGCATGA | 25879 |
rs569459433 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437174 | TCTCCAAATTGTCAT[G/T]AGTGTTTTTTTGGCA | 25879 |
rs569555460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421786 | TTATCCATGTTGTAG[C/T]ACATGTCAGAATTTC | 25879 |
rs569641051 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433442 | CTTATCTTTTTTTTT[-/C]CCAAAGCATTTATTA | 25879 |
rs569704782 | snp | A/C | 9.02812e-05 | 0.00671807 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442870 | GAAACACGTAGTGGC[A/C]GTTGTAAAATAATTG | 25879 |
rs569790775 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429216 | TAGAAATGGAACCTG[G/T]TCAGACCCTGAGGCG | 25879 |
rs570064935 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414308 | TTGTACCATTCTACA[A/C]ATGCCAAAAAACAAA | 25879 |
rs570102401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419262 | TTCTGGAGCCATACT[A/G]CCTTGGTTTGAATCC | 25879 |
rs570141122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419901 | GTAATCCCAGCTACT[A/C]GGGTGGCTGAGGCAG | 25879 |
rs570188831 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414704 | AACGCTCCTCCTCCC[C/T]CTAGAACGGAAAAGA | 25879 |
rs570224632 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415710 | AAAGTCTGTTCAAGT[C/G]CTTTTTCTAAGAATT | 25879 |
rs570376894 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413905 | GTATTTCTTGATTTT[A/G]TGTTGTCTAGAATTA | 25879 |
rs570380346 | snp | C/T | 5.02449e-05 | 0.00501198 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420252 | TATTAAGAAGGATCA[C/T]TCTTATTTCAGTTCC | 25879 |
rs570478887 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424793 | TTTGGGTCAAGCCAG[A/G]TCAGTCAAGACCTGG | 25879 |
rs570576578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430525 | TTAACATAAATATTA[A/G]GGGCAATTAAATCAT | 25879 |
rs570590386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440366 | TAGGTATTTTTGGGT[A/G]TTTTGATTAAATTGA | 25879 |
rs570619078 | snp | G/T | 0.000520544 | 0.0161245 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432782 | GTGTATTTCTATCAT[G/T]AATGGCTTAATTGTA | 25879 |
rs570624479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439905 | AGTTTGTTCATATTT[A/G]TTTCTCTTACTAGAT | 25879 |
rs570728140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433445 | ATCTTTTTTTTTCCC[A/C]AAGCATTTATTATAG | 25879 |
rs570763195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426328 | TTGATGCTAAAGAAT[C/T]TTAACAGTTTTTTTT | 25879 |
rs570788770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425802 | TGTTTATCACAATAT[A/G]CATGACCTAACTTTG | 25879 |
rs570829163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438714 | TTAGAGATATTTTTT[A/G]TAGATATGAATATTT | 25879 |
rs570858683 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438045 | GAAGTTAAGAACTCA[C/G]CATAGTTTACCATTG | 25879 |
rs570942909 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421704 | TTAAAGAATTATACC[A/G]TTTTGTGTATGTGGA | 25879 |
rs571077123 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418525 | GTGACAGAATGATAC[C/T]GCATCTCAAAACAAA | 25879 |
rs571081488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436235 | AATAAAGTTTTTTGC[C/T]CCAATACAGTTTAAG | 25879 |
rs571105642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417845 | ATCTGATAGGCTGGG[C/T]GCAGTGGCTCACGCC | 25879 |
rs571307417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429963 | ATTCAAAAGAAGAAC[A/T]ACGTGGGGGGGAAAT | 25879 |
rs571309990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417122 | TGAACCAGTCCCACT[C/G]TTTAAGAGGTTTACA | 25879 |
rs571345928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423327 | TGGATGAATGAATTT[A/T]AAAAAAAAAAGTACA | 25879 |
rs571564019 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433634 | GATGTTTTAGTGGTA[C/T]CAACTAAAAGCATCT | 25879 |
rs571660959 | snp | A/C/G | 8.37649e-05 | 0.00647122 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415237 | CACGGACGCGGAAGC[A/C/G]ACTGCACAGCTAAAG | 25879 |
rs571699950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432464 | TGAGATTAGGAGACT[A/G]GGAGTTAAGCATTTC | 25879 |
rs571737594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432966 | GACAGTAAACAACTC[A/G]TGGACCAAATCCTTT | 25879 |
rs571744345 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443281 | CCTGTGATTCCACAT[A/G]ACATTTAGAATAATG | 25879 |
rs571780284 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442262 | TTTCTGATGTAGCTG[A/G]AATTAAGAGATTTTG | 25879 |
rs571814921 | snp | C/T | 0.000201882 | 0.0100449 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427284 | AGTATGTTTTACTTA[C/T]TATGGCTTAATAATT | 25879 |
rs571839159 | snp | A/G | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443473 | GGCCTATTTTTGGTA[A/G]ATAATTTTCAATCTC | 25879 |
rs571892184 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417805 | AAGCATGGGAGTGAC[A/G]TGTAAAAAGCTGTTT | 25879 |
rs571970372 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440608 | TCAGAACTTAGAGCT[C/T]GTATCTCTTGTTAGA | 25879 |
rs571973728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429357 | ACATTAGCTTTATGA[C/T]GTGTTATTTGAATTG | 25879 |
rs572050499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419571 | AATGTTCCCTGCCCT[A/G]CAGGAAGCTTAGAGT | 25879 |
rs572177794 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412904 | CATGGAAGCATAAAA[A/T]TTATAGTATGTTACT | 25879 |
rs572189006 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413966 | ATTAAATTCTAAGTT[C/T]CCTGAAGGCAAGAAC | 25879 |
rs572216362 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412945 | GTTGATAATCAATAA[A/C]TTTTTATTTCGTTAT | 25879 |
rs572283807 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414559 | GGATGTTTTTTCTCA[G/T]ACTTCTCTACATACA | 25879 |
rs572451562 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437845 | AGTATTTGAAAGTAG[A/G]CTTCTGTTGGAAGTT | 25879 |
rs572473870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418791 | ACTGAGTTTTTTTAG[A/G]CATACGAGCTTAAAA | 25879 |
rs572858345 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425223 | AACTAGCAGTTTTGT[A/G]TGTATGCAGTTATAC | 25879 |
rs572895810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435919 | ACTTAAACAAAACTA[A/G]ATGGTATAACGTGTT | 25879 |
rs573059391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425240 | GTATGCAGTTATACA[A/G]TACCACATTTATGAT | 25879 |
rs573104703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430835 | CTCTACATGATGATA[A/G]TCATGTTCTTTCAGC | 25879 |
rs573105035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439106 | TCCGCCTCCTGGGTT[C/T]ACGCCATTCTGCCTC | 25879 |
rs573142804 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103431381 | CTGGACATCATTGAG[A/T]TGCCACAAGTCTGTT | 25879 |
rs573244603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429574 | GGCTTATTTTTACTT[A/T]ATGCCAAGGGGTTAT | 25879 |
rs573379439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103423034 | CTGTCAAAAAGCAGA[A/G]TAGGCTACCTTGCAA | 25879 |
rs573429206 | in-del | -/CCAG | 0.00279162 | 0.0372561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103433726 | TTGGGCCACTGCACT[-/CCAG]CCTGGCCAACAGAAC | 25879 |
rs573510361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416107 | CAAGGGACCAACCAT[A/G]CGTAAGCAGATTGTT | 25879 |
rs573546573 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423134 | AGGAATTGATTGGCA[A/G]GTGGGAATGGATGGC | 25879 |
rs573548626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416692 | ATGATTATTATTTTG[A/G]TTAATAGTCTTTCCC | 25879 |
rs573578528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428184 | ATGCTGCAGTGCGAT[A/G]TGAGCTTGGCCTTGA | 25879 |
rs573891207 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438207 | AAAAGGGCTTCTTAG[C/G]TATGTGGAGATTATA | 25879 |
rs574073876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103439235 | TGACCTCGTGATCCA[C/T]CTACTGCAGCCTCCC | 25879 |
rs574131797 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414421 | AACCACGTGGGTATG[C/G]TAAGATTTCAAAGTT | 25879 |
rs574264462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441877 | TTCATGCCATTCTCC[C/T]GTCTCAGCCTCCTGA | 25879 |
rs574372984 | in-del | -/TTTC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442740 | TTTTTCTGAGAAAGT[-/TTTC]TTTAAGATGAGTTCC | 25879 |
rs574408960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432336 | TCTTTATGTTAACCC[C/T]AAGCTCACCATTAAT | 25879 |
rs574423410 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420206 | CAGAGTGATTAGCTG[A/C]GGAAGACTGCAGGAA | 25879 |
rs574566917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103417392 | TATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 25879 |
rs574740361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430783 | AGCAAATATTTTCTC[A/C]GAATTAAAAAAATCT | 25879 |
rs574758144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103419490 | CAGTAAATGATAGCT[A/G]TATAATATCATCATA | 25879 |
rs575131956 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440289 | AAGAGAATTCATTTT[A/C]TTTCATTGTCATAAA | 25879 |
rs575211316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442629 | AGCAATTAAATAAGT[A/G]AAGTTGATTTCTTGG | 25879 |
rs575351102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416599 | TGTTCCTGCTTACCT[C/G]CTGCATGAGCCCCGC | 25879 |
rs575411801 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437480 | GTAGGTCTAGCTAGA[A/G]AACTCACATTATTCC | 25879 |
rs575455025 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430248 | ATACAAAATATTAGC[C/G/T]CGGTGTGGTGGCGCA | 25879 |
rs575561482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438129 | GCATGAACAGATTAT[C/G]TTTAATGGTTACGGA | 25879 |
rs575631700 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426638 | TTTTAGCATAAGAAT[A/T]ATTTAGAACATTTGG | 25879 |
rs575695370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428124 | TAAGGTTGAGTCAAA[A/G]TAGTAAGGTATAAAA | 25879 |
rs575737565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103436390 | ATTTCACTTTAGTAG[G/T]TATATGGCTTGGTTG | 25879 |
rs575887728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425732 | TTTTGAATGACTAAC[C/T]AGATATTATAATACC | 25879 |
rs575969801 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442205 | ATAAGAAAACACTTG[C/T]TCATATTAAAAAATT | 25879 |
rs576022917 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438411 | CCAGTTTTGTGAGTA[C/T]AGTCGAGAGATTTTT | 25879 |
rs576059303 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414582 | TACATACATGCCCCC[C/T]CTCTTAGTCTTGAGG | 25879 |
rs576161899 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441238 | GCTTTCTACTGGGTG[G/T]CATCTATCTACATGG | 25879 |
rs576324827 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415331 | CAGGCCGCCGCTCCG[C/G]GAGTCACGTGACTGG | 25879 |
rs576574354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440855 | TCTATAAGAAACAGA[C/G]TGTTTATATTAGAAA | 25879 |
rs576797357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103438452 | TTGAGACAGAGTCTG[C/G]CTCTGTCAGCCAGGC | 25879 |
rs576816720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF13 | GRCh38.p7 | 8:103429599 | GGTTATGTGAGTACC[A/G]TGCACATTTATAATT | 25879 |
rs576925804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103424444 | CAGTGTTGCAAAACA[C/T]AAACTTTTATTACCT | 25879 |
rs577136600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425447 | CTGTCAGCACAGTGA[A/G]AAGACAAACTATGTC | 25879 |
rs577166294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103437420 | CAAGGGGCCAGCAGC[G/T]GAGTTCAGGCTGAAT | 25879 |
rs577175040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103425949 | AATACTGGAATGATA[C/T]GGTATGTTACCTGTT | 25879 |
rs577209835 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | DCAF13 | GRCh38.p7 | 8:103418844 | TATATATATATATAT[A/T]TATATATATATATAT | 25879 |
rs577268589 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416846 | ACATGAAGAGATTTA[G/T]AAACAAAATGATCTA | 25879 |
rs577273600 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414633 | GACCCCTCCACCAAG[A/C]ACCATTTCCTCAAAT | 25879 |
rs577644749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415952 | AGACAAAGATGAATT[C/T]AAAAGCATCAGTTTT | 25879 |
rs577974312 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434953 | TTGGCAACTCAAATC[A/G]AGCCTAAAAATGCTC | 25879 |
rs578163618 | snp | A/G | 0.000136193 | 0.00825095 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421298 | AATATTCAATTTACC[A/G]CAAAAGTGGAATTAA | 25879 |
rs578211342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103434575 | TTTCTCCACTAAAGA[C/G]TTACTTTTTTTTCCT | 25879 |
rs578232140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF13 | GRCh38.p7 | 8:103428225 | AGAAGTCAGAGGACA[C/T]TCTTCCTGCAACTAC | 25879 |
rs745462693 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427257 | ACCCAATTGAGGTAA[G/T]GTTTTTTTTTAAGTA | 25879 |
rs745464525 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415695 | GGATGGATAGCAAGT[A/G]AAGTCTGTTCAAGTC | 25879 |
rs745489735 | in-del | -/TG | 1.6537e-05 | 0.00287545 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103426073 | TGGTGATGACAAAAC[-/TG]TGAAGCAGTGGAAAA | 25879 |
rs745538836 | snp | A/G | 7.25019e-05 | 0.00602044 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414863 | CACGCCCGCTATCAG[A/G]TTCTCATACCGGACG | 25879 |
rs745550032 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416432 | CCACCTTCCTTGCCA[C/G]TTTAGTCAGTCACTA | 25879 |
rs745653877 | snp | A/G | 0.00032437 | 0.0127311 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414951 | ATAGGCTCGGGGCCC[A/G]TCGACACCACGGCGC | 25879 |
rs745661380 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417147 | TTTACAGTGATTGAA[A/G]TCACATCTGTTAACC | 25879 |
rs745740639 | snp | A/G | 1.68545e-05 | 0.00290292 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103440151 | GGAGGTATATCATAC[A/G]AAGAGAATGCAACAT | 25879 |
rs745753981 | snp | A/C | 1.64768e-05 | 0.00287021 | missense | DCAF13 | GRCh38.p7 | 8:103421020 | TGTATCCGTACAATA[A/C]AAGCACATGAAGGCT | 25879 |
rs745795302 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434545 | GATCATTTGGTTAGG[G/T]TGGTGTCTGCCAGGT | 25879 |
rs745814983 | snp | A/C | 1.65968e-05 | 0.00288065 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421095 | ACTGTAAGTATAATA[A/C]CATTAAGTCATTAAA | 25879 |
rs745903352 | in-del | -/AGA | 1.88995e-05 | 0.00307398 | cds-indel | DCAF13 | GRCh38.p7 | 8:103442848 | TGCCACTTGTGTCAG[-/AGA]AGAAGAAACACGTAG | 25879 |
rs745933652 | snp | A/G | 5.03267e-05 | 0.00501606 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426012 | AAGTTTTAATTTATA[A/G]CTGTTGTTCCTTACC | 25879 |
rs746039451 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413046 | GCTTCCACTCCTGGA[C/T]CTTTAATTTAGGCCT | 25879 |
rs746061769 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419180 | TGAGCCACCACGCCC[A/G]GCCCTAAGCGTGATT | 25879 |
rs746102842 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436061 | GTTTATGTAAACATA[C/T]ATAAACACAGGAAAA | 25879 |
rs746138680 | snp | A/G | 1.64876e-05 | 0.00287116 | missense | DCAF13 | GRCh38.p7 | 8:103430660 | AATATAGTACTGTAC[A/G]ATATGAGGCAAGCTA | 25879 |
rs746216860 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430940 | GATGCCAGTACATTT[C/T]AGGCCTCTAATTAAT | 25879 |
rs746228451 | snp | A/T | 1.66654e-05 | 0.00288659 | missense | DCAF13 | GRCh38.p7 | 8:103432692 | ACAAATACAATCTGT[A/T]GGAACCCTATGGAAG | 25879 |
rs746248488 | in-del | -/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425632 | TGCCTTCTCTCCAGT[-/G]ATTTTCATGTTTTTC | 25879 |
rs746318456 | snp | G/T | 1.6623e-05 | 0.00288292 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420376 | ACCATTCCTTGCTTC[G/T]CTGGATGGTCACCGT | 25879 |
rs746422282 | snp | A/C/T | 1.72445e-05 | 0.00293632 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415115 | CTAGTACTGAGGGGG[A/C/T]AAGAACGGGGCACAG | 25879 |
rs746483356 | snp | A/C | 1.6884e-05 | 0.00290547 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415471 | AAGATGCTGAGCCGG[A/C]ATCCGGACAATTATG | 25879 |
rs746546869 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440832 | GTTTTTCTAAATGTC[C/T]CATATTTTCTATAAG | 25879 |
rs746571278 | snp | G/T | 0.00012285 | 0.00783645 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415560 | CGGTTTCCGCAAGTC[G/T]TTGGGTCTAGCCTCG | 25879 |
rs746574905 | snp | A/G | 1.6947e-05 | 0.00291088 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414971 | CACCACGGCGCCCAG[A/G]GCCGCGGAGGTGGGA | 25879 |
rs746663173 | snp | A/C | 6.15795e-05 | 0.00554851 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415042 | GTGAGCGCAACCCCA[A/C]CTCCGGGACCAACGA | 25879 |
rs746697781 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434426 | TAAAGCATCTTACTA[A/G]AAAGCAGTTTGCTGG | 25879 |
rs746716988 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103440181 | TGTTATCTGTGTAAA[A/G]TGGACTTCTGACAGC | 25879 |
rs746806965 | snp | A/G | 1.73586e-05 | 0.00294601 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441415 | ATACTGAAGCAAAAC[A/G]ACACACTATTCATTA | 25879 |
rs746894856 | snp | A/G | 1.67024e-05 | 0.0028898 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426028 | CTGTTGTTCCTTACC[A/G]TCATCATAATAAAAC | 25879 |
rs746895157 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423360 | CACACACGCACACAG[A/G]AATACTATTCAGCCT | 25879 |
rs746986388 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413147 | CAAGACTATTAATCT[C/T]CTCAGGTACCAAGAA | 25879 |
rs747047776 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435930 | ACTAGATGGTATAAC[A/G]TGTTGCACACCTAGG | 25879 |
rs747049781 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419136 | TGATCCGTCCGTCCC[A/G]GCCCCCCAAAGTGCT | 25879 |
rs747074214 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414354 | TATTCTAAATCTACT[C/G]CCAACCATTCGCTGA | 25879 |
rs747184044 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431136 | TTCAGTTACATGCTG[A/G]TCAATACTAGTTTGA | 25879 |
rs747222367 | snp | A/G | 1.84154e-05 | 0.00303436 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435614 | GTCAAATATTTAAAA[A/G]TTCTTTTACAGCTTA | 25879 |
rs747280127 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432354 | GCTCACCATTAATTT[C/T]GCCCCTAATTTGATA | 25879 |
rs747306618 | snp | A/C/G | 9.64239e-05 | 0.00694294 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420512 | AAGTAGTTATATTAC[A/C/G]AATGTTTTCCCTTTA | 25879 |
rs747344058 | snp | A/C/G | 5.16581e-05 | 0.00508201 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415118 | GTACTGAGGGGGCAA[A/C/G]AACGGGGCACAGACA | 25879 |
rs747433025 | snp | A/C/T | 6.58928e-05 | 0.00573957 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441568 | TCTACCAAAATCTAT[A/C/T]TATAGCCAGATTCAG | 25879 |
rs747434075 | snp | C/T | 1.69622e-05 | 0.00291219 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415157 | CGCCGGCGGAAAGCG[C/T]GATGGAGGGGAGGTC | 25879 |
rs747471942 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441037 | TCATCCTTAACATTC[A/G]TTAAACAAAGGGTAG | 25879 |
rs747588323 | snp | A/G | 4.95299e-05 | 0.00497619 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420349 | TACCAAACTGGAACG[A/G]GTATTTGCAAAACCA | 25879 |
rs747599439 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441639 | TTTTGAGGCATTTGA[C/T]TCTATTACCCTTTTC | 25879 |
rs747668941 | snp | A/T | 1.84561e-05 | 0.00303772 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415059 | TCCGGGACCAACGAG[A/T]GGACTCTTATGCCCA | 25879 |
rs747686018 | snp | C/G | 1.73273e-05 | 0.00294335 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441421 | AAGCAAAACAACACA[C/G]TATTCATTAAGATAC | 25879 |
rs747774061 | snp | C/T | 1.65649e-05 | 0.00287788 | missense | DCAF13 | GRCh38.p7 | 8:103426057 | ACAAATATTTCTAGG[C/T]TGGTGATGACAAAAC | 25879 |
rs747802770 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423647 | CATGCTCTCTTGACA[A/G]TTGCTATGAAAGTGA | 25879 |
rs747906254 | snp | C/G | 1.67618e-05 | 0.00289493 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415322 | TTGAGCCAGCAGGCC[C/G]CCGCTCCGCGAGTCA | 25879 |
rs747917203 | in-del | -/A | 4.94984e-05 | 0.00497461 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441642 | GAGGCATTTGACTCT[-/A]ATTACCCTTTTCTGA | 25879 |
rs747943082 | snp | C/T | 1.66649e-05 | 0.00288655 | missense | DCAF13 | GRCh38.p7 | 8:103426128 | GAGGAAGAGCCATTA[C/T]ATACAATATTAGGAA | 25879 |
rs747969827 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424874 | GTTTTAGTATAGTGC[C/T]AGTGGCTCAGATTCA | 25879 |
rs747990676 | snp | C/T | 1.66366e-05 | 0.0028841 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415364 | GTAGTCTGGGAAAAG[C/T]GGAAGTCGCCTGTGG | 25879 |
rs748056048 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416097 | ACCTAAATGACAAGG[A/G]ACCAACCATGCGTAA | 25879 |
rs748059527 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414399 | CCCAATACTAGTCGA[C/G]CTGCCAAACCACGTG | 25879 |
rs748078750 | snp | G/T | 3.40205e-05 | 0.00412421 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414770 | TGCAGCCCGGTGTCT[G/T]GGCGGGCTCTTACCG | 25879 |
rs748119605 | in-del | -/T | 1.94685e-05 | 0.00311992 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427271 | ATGTTTTTTTTTAAG[-/T]ATGTTTTACTTATTA | 25879 |
rs748179004 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432516 | GCCTGTGTATTTAAG[A/G]AGCAATTACTGATTG | 25879 |
rs748186998 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414476 | GTGTGAGGACTAAAC[C/T]TTAAAATGTGACAAT | 25879 |
rs748230776 | snp | C/T | 1.80289e-05 | 0.00300235 | missense | DCAF13 | GRCh38.p7 | 8:103435630 | TTCTTTTACAGCTTA[C/T]ATACTTTTGATATGC | 25879 |
rs748328766 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420154 | TTCTTAGTGTTAGGC[A/G]TAGAACAATGTCACT | 25879 |
rs748341631 | snp | A/C | 3.58641e-05 | 0.00423448 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420543 | GTTTTTAGTTACTGT[A/C]GGTTTTACTTTATTG | 25879 |
rs748408774 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | DCAF13 | GRCh38.p7 | 8:103421005 | CTAACTCAGCGGAAT[C/T]GTATCCGTACAATAC | 25879 |
rs748438846 | snp | C/G | 1.68411e-05 | 0.00290177 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415204 | CTCCGCCCTGCCTCG[C/G]CCACAAATGCTCCAG | 25879 |
rs748444696 | snp | A/T | 1.65059e-05 | 0.00287275 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441651 | TGACTCTATTACCCT[A/T]TTCTGACTTCTGCTC | 25879 |
rs748540892 | snp | C/T | 4.95078e-05 | 0.00497508 | missense | DCAF13 | GRCh38.p7 | 8:103427161 | CATGTGGACAGCAAG[C/T]AGACATTTGGGATGA | 25879 |
rs748552164 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424482 | CACTAAGATATACCA[C/G]TTTGTAATACCAACA | 25879 |
rs748592005 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422713 | TATACAACAGTTTTT[A/G]TATACACATGCGCTA | 25879 |
rs748625915 | snp | A/G | 1.8333e-05 | 0.00302757 | missense | DCAF13 | GRCh38.p7 | 8:103442826 | AAACACAGCAAGCCT[A/G]GATCTGTGCCACTTG | 25879 |
rs748660207 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438344 | TTAAAAATGAATTTC[A/T]AATGGTTTATCAAAG | 25879 |
rs748707587 | snp | A/G | 5.92891e-05 | 0.00544436 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427272 | TGTTTTTTTTTAAGT[A/G]TGTTTTACTTATTAT | 25879 |
rs748736027 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427570 | CTTCATGTTCCATAG[A/G]TTATGTCATTGTACA | 25879 |
rs748777709 | snp | A/G | 1.69545e-05 | 0.00291152 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415143 | CAGACACTACGTCAC[A/G]CCGGCGGAAAGCGCG | 25879 |
rs748808070 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427802 | TAAGGGAAGAGTTGG[A/C]GATTGGCCACTACAT | 25879 |
rs748833131 | snp | G/T | 1.77483e-05 | 0.0029789 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426164 | CAAAAGTAAATTGAC[G/T]AATAGCTTGCCTATT | 25879 |
rs748838971 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441261 | CTACATGGCGAGTGT[A/G]TTGCCTAAAAGGAAA | 25879 |
rs748882760 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441623 | CGTCGACGAAAGTAT[A/G]TTTTGAGGCATTTGA | 25879 |
rs748993515 | snp | A/G | 3.30311e-05 | 0.0040638 | missense | DCAF13 | GRCh38.p7 | 8:103427122 | CTGGGATTGATCATC[A/G]CTGGAAAGAAGCTGT | 25879 |
rs749045775 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414169 | ATCAAAGATCATCTT[G/T]GAAACTCTTTCCAGA | 25879 |
rs749105713 | in-del | -/C | 1.71239e-05 | 0.00292603 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414740 | GAGATCCAGTTCGGG[-/C]TGACAGTGAGAGGAT | 25879 |
rs749158347 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433982 | CAAGGTACCGTTTTT[C/G]AGAGTGTCCTCGGAA | 25879 |
rs749180359 | snp | C/T | 5.30237e-05 | 0.00514869 | missense | DCAF13 | GRCh38.p7 | 8:103435645 | TATACTTTTGATATG[C/T]GTGCACTGGACACTC | 25879 |
rs749205095 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103435770 | TATTCGAATCTTTCC[C/T]GTAGACAAAAGTCGA | 25879 |
rs749232294 | snp | A/G | 3.07858e-05 | 0.00392326 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414945 | CCCGTCATAGGCTCG[A/G]GGCCCGTCGACACCA | 25879 |
rs749433773 | snp | A/G | 3.36366e-05 | 0.00410088 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415210 | CCTGCCTCGCCCACA[A/G]ATGCTCCAGCCCACG | 25879 |
rs749435725 | snp | C/T | 4.95201e-05 | 0.0049757 | missense | DCAF13 | GRCh38.p7 | 8:103421077 | TGTGGGACTTCTTTT[C/T]TCACTGTAAGTATAA | 25879 |
rs749469380 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422507 | AATCTGTGAATGAGC[A/C]TAGTGTCCTAGGAGG | 25879 |
rs749564756 | snp | C/T | 1.83964e-05 | 0.0030328 | missense | DCAF13 | GRCh38.p7 | 8:103442833 | GCAAGCCTGGATCTG[C/T]GCCACTTGTGTCAGA | 25879 |
rs749644909 | snp | A/G | 2.34667e-05 | 0.00342532 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427289 | GTTTTACTTATTATG[A/G]CTTAATAATTTCAGT | 25879 |
rs749736452 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103430638 | GGGAAGTTGTGCATC[C/T]GACAGGAATATAGTA | 25879 |
rs749746739 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429373 | GTGTTATTTGAATTG[C/T]GTACAGACAGTAGGA | 25879 |
rs749832195 | snp | A/T | 1.71696e-05 | 0.00292993 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420226 | GACTGCAGGAAATAT[A/T]AAGTGTGAATTATTA | 25879 |
rs749833684 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417383 | GTGGTGGCTTATGCC[C/T]GTAATCCCAGCACTT | 25879 |
rs749835638 | snp | C/T | | | missense | DCAF13 | GRCh38.p7 | 8:103430678 | ATGAGGCAAGCTACT[C/T]CTTTGAAAAAGGTGA | 25879 |
rs749898926 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417577 | AACCCAGGAGGCAGA[C/G]CTTGCAGTGAGCCGA | 25879 |
rs749911495 | in-del | -/CTT | 1.65194e-05 | 0.00287392 | cds-indel | DCAF13 | GRCh38.p7 | 8:103440186 | TCTGTGTAAAATGGA[-/CTT]CTGACAGCAAGTATA | 25879 |
rs750018870 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441314 | TTACTAATATAACCT[C/T]GTAAAGTGCAGAATT | 25879 |
rs750030245 | snp | A/G | 2.7868e-05 | 0.00373272 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442894 | ATAATTGGTATTCCT[A/G]ACAATCCTGATGTAT | 25879 |
rs750107420 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433850 | TTAACCTTTATTGAT[A/G]TTTTGAAATTAAGTG | 25879 |
rs750126173 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428718 | CGTACTAAAAAAAAA[A/C]CACAAAAAAACCTAA | 25879 |
rs750135792 | snp | G/T | 1.65416e-05 | 0.00287586 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430589 | TCTGGCTTTGAACTG[G/T]TGATTGTTATACTTG | 25879 |
rs750189562 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438371 | AAAGTGCTTAAAACA[A/T]ACCTATCAGAAACAG | 25879 |
rs750217561 | snp | A/G | 8.29538e-05 | 0.00643972 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430733 | TACAGTTGGCATTAT[A/G]TATTTCTCTGTAAAT | 25879 |
rs750253444 | snp | A/G | 0.000523423 | 0.016169 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415036 | CCCCTTGTGAGCGCA[A/G]CCCCACCTCCGGGAC | 25879 |
rs750347003 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426840 | AAAGGGATAGGGGAA[C/T]GGGGTATGAGTATGA | 25879 |
rs750385901 | snp | C/G | 1.75999e-05 | 0.00296642 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415086 | CCCAAGGCGCGTGAG[C/G]GAAGCCGGAGACTCT | 25879 |
rs750402182 | in-del | -/TTC | | | cds-indel | DCAF13 | GRCh38.p7 | 8:103443124 | TTTGCAACTCATTTT[-/TTC]TTGTTTTTATTACAG | 25879 |
rs750474129 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441493 | CAAGGATTATAACCA[A/G]AAATTGAAGGAGAAA | 25879 |
rs750520729 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437929 | TTAGTGTGACTGTGT[A/G]TATAAAGAATTTAAG | 25879 |
rs750580568 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424309 | TGGGATTACAGGCGC[A/G]AGCCGCCATGCCCAA | 25879 |
rs750616498 | snp | A/G | 6.66756e-05 | 0.0057735 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415349 | GTCACGTGACTGGAA[A/G]TAGTCTGGGAAAAGC | 25879 |
rs750753908 | snp | A/G | 1.66261e-05 | 0.00288319 | stop-gained, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415395 | GAGGAGGTGGCGGTG[A/G]GCGGAACTCCTAGCG | 25879 |
rs750767608 | snp | A/T | 1.70889e-05 | 0.00292304 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414751 | CGGGCTGACAGTGAG[A/T]GGATGCAGCCCGGTG | 25879 |
rs750774658 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415130 | CAAGAACGGGGCACA[C/G]ACACTACGTCACGCC | 25879 |
rs750886891 | snp | C/T | 1.87883e-05 | 0.00306493 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435596 | ATCTTTCTAGAAATA[C/T]GTGTCAAATATTTAA | 25879 |
rs750911114 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432945 | TTTAGAATGATGTAG[A/G]CCAGGGACAGTAAAC | 25879 |
rs750926513 | snp | A/T | 1.66012e-05 | 0.00288103 | missense | DCAF13 | GRCh38.p7 | 8:103435706 | CAGTGCTTGATGTGG[A/T]TTACTCTCCCACTGG | 25879 |
rs750935146 | snp | A/G | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443669 | CTGTATCTGTGGGAG[A/G]TTGATTTCAAGATGT | 25879 |
rs750960048 | snp | A/G | 0.000122752 | 0.00783333 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420479 | GCAAGTGTCAATCTA[A/G]ATGATATTTTCAACT | 25879 |
rs750999874 | snp | A/T | 1.64996e-05 | 0.0028722 | missense | DCAF13 | GRCh38.p7 | 8:103430617 | TTGTTTTTAGACATT[A/T]CTCTTGGGAAGTTGT | 25879 |
rs751084635 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant, utr-variant-5-prime | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413504 | TCCTCATCTGTATAG[C/G]AGATATCATAAACTC | 25879 |
rs751136586 | snp | A/G | 1.7086e-05 | 0.00292279 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432624 | GAAAAGAAAAGGAAA[A/G]GAAGTGGGAAATTCA | 25879 |
rs751174126 | snp | C/T | 1.70502e-05 | 0.00291972 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432770 | TTTTAAAAACTTGTG[C/T]ATTTCTATCATGAAT | 25879 |
rs751224801 | snp | C/G | 1.64999e-05 | 0.00287222 | missense | DCAF13 | GRCh38.p7 | 8:103420341 | TTAAATGCTACCAAA[C/G]TGGAACGAGTATTTG | 25879 |
rs751255616 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418749 | GGATGAAGTCATGGG[C/G]TAAGAAGATGCATTT | 25879 |
rs751350298 | snp | A/G | 3.48329e-05 | 0.00417316 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415096 | GTGAGCGAAGCCGGA[A/G]ACTCTAGTACTGAGG | 25879 |
rs751436268 | snp | C/G/T | 5.08232e-05 | 0.00504078 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415134 | AACGGGGCACAGACA[C/G/T]TACGTCACGCCGGCG | 25879 |
rs751526681 | snp | A/G | 1.65954e-05 | 0.00288053 | missense | DCAF13 | GRCh38.p7 | 8:103426119 | TATGGAGACGAGGAA[A/G]AGCCATTACATACAA | 25879 |
rs751532727 | snp | C/T | 9.88419e-05 | 0.00702931 | missense | DCAF13 | GRCh38.p7 | 8:103441597 | AGGAACAGCGCATCA[C/T]GAAAGAAGCTCGTCG | 25879 |
rs751613260 | snp | A/T | 3.35542e-05 | 0.00409585 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427076 | ATGAAAAAAATCCTC[A/T]TAACCTTTTTGCTTT | 25879 |
rs751644254 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425674 | TACATTTAAAATTAC[C/G]TGGAATTTTATTTTC | 25879 |
rs751653083 | snp | C/T | 1.66371e-05 | 0.00288414 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415405 | CGGTGGGCGGAACTC[C/T]TAGCGGACACCTCGT | 25879 |
rs751654522 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437364 | AAAAGAATGAAACGA[C/G]AACAAAGAAAAAAAC | 25879 |
rs751665235 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426707 | GCAAACAATTCCAAA[A/G]TTAGATTTAATCTTT | 25879 |
rs751713374 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415247 | GAAGCGACTGCACAG[C/T]TAAAGAACCGCCCCT | 25879 |
rs751832875 | snp | G/T | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443330 | TGAATTTATTTCTAG[G/T]GCTTTACTTATATTT | 25879 |
rs751908054 | snp | A/C | 1.65583e-05 | 0.00287731 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414925 | CGGACGCCGACTGGC[A/C]CTGGCCCGTCATAGG | 25879 |
rs751921711 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430347 | CAGTGAGCCAAGATT[A/G]CACCACTGCACTCCA | 25879 |
rs751926148 | snp | C/G | 1.65078e-05 | 0.00287291 | missense | DCAF13 | GRCh38.p7 | 8:103435738 | AAGGAGTTTGTGTCT[C/G]CTAGTTTCGATAAAT | 25879 |
rs752015905 | snp | A/T | 1.64822e-05 | 0.00287068 | missense | DCAF13 | GRCh38.p7 | 8:103420997 | TTTGGAATCTAACTC[A/T]GCGGAATTGTATCCG | 25879 |
rs752035456 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422076 | CAGGCAATAATAAGA[A/G]GCTACCTTATTATGG | 25879 |
rs752082252 | in-del | -/G | 1.65299e-05 | 0.00287483 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435805 | GGTATGTGCCTACCA[-/G]TAAGCCATTTATATT | 25879 |
rs752280024 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419870 | AAAAATTAGCTGGGC[A/G]TGGTGGCATGCGCCT | 25879 |
rs752299153 | snp | A/C | 0.00014887 | 0.00862628 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420964 | AAATTTCCTGGTATG[A/C]CTTATCATAGGTTAG | 25879 |
rs752299834 | snp | C/T | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443806 | ATTACTTATAATACC[C/T]AATACAATGTAAATG | 25879 |
rs752405404 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | DCAF13 | GRCh38.p7 | 8:103441612 | TGAAAGAAGCTCGTC[A/G]ACGAAAGTATGTTTT | 25879 |
rs752439573 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420581 | ATTTACTTCTCAAGA[C/T]TAAATTTCGTTAGGA | 25879 |
rs752455755 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437029 | TTATCTGATTATGAA[G/T]GTGCTTCAGTTAGAA | 25879 |
rs752491312 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435861 | CATTCTGAGAAATGA[A/G]TCATTGGGCGATTTC | 25879 |
rs752518262 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425795 | AATGCCATGTTTATC[A/T]CAATATGCATGACCT | 25879 |
rs752596170 | snp | C/T | 7.06739e-05 | 0.00594407 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442783 | CTTATATTTTGTATA[C/T]TTTATTTCTAGGGAA | 25879 |
rs752635374 | snp | A/G/T | 9.9836e-05 | 0.00706463 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415410 | GGCGGAACTCCTAGC[A/G/T]GACACCTCGTGGAGT | 25879 |
rs752698080 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428181 | GAGATGCTGCAGTGC[A/G]ATGTGAGCTTGGCCT | 25879 |
rs752723394 | snp | C/T | 1.66682e-05 | 0.00288684 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415431 | CTCGTGGAGTCCGGC[C/T]GGAAGAGCAACCGAG | 25879 |
rs752800901 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416202 | AGGGCTGTGTCATTA[C/G]TTTGAATGAGGAGTA | 25879 |
rs752932122 | snp | C/T | 3.10015e-05 | 0.00393698 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415015 | CCGCCACCGTGGCGA[C/T]GGTCGCCCCTTGTGA | 25879 |
rs753062391 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440786 | TACCTCCAGGATAGG[A/G]GATTATGGTTGATTT | 25879 |
rs753069593 | in-del | -/CTGAGTGCTGTTATATACTTTCATTAGAGGCACA | 1.66377e-05 | 0.00288419 | frameshift-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415354 | TGACTGGAAGTAGTC[lengthTooLong]TGGGAAAAGCGGAAG | 25879 |
rs753088008 | snp | G/T | 3.34504e-05 | 0.00408951 | missense | DCAF13 | GRCh38.p7 | 8:103440267 | CTTCTGAAAAATTGG[G/T]TGTGGTAAGAGAATT | 25879 |
rs753097995 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422187 | GGTTCCTGTTGCTGA[A/G]GAGTACCAGCAAGTT | 25879 |
rs753110747 | in-del | -/C | 3.38796e-05 | 0.00411566 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415134 | AACGGGGCACAGACA[-/C]TACGTCACGCCGGCG | 25879 |
rs753168508 | snp | A/G | 1.67413e-05 | 0.00289316 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415246 | GGAAGCGACTGCACA[A/G]CTAAAGAACCGCCCC | 25879 |
rs753170138 | snp | C/T | 1.66092e-05 | 0.00288172 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442919 | ATGTATAATTATTTG[C/T]TACTTTTGATTTGAG | 25879 |
rs753177667 | snp | A/T | 5.72164e-05 | 0.00534836 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421284 | AACATGATTAAACTA[A/T]TATTCAATTTACCAC | 25879 |
rs753328868 | snp | A/C | 1.64977e-05 | 0.00287203 | missense | DCAF13 | GRCh38.p7 | 8:103420980 | CTTATCATAGGTTAG[A/C]ATTTGGAATCTAACT | 25879 |
rs753414680 | snp | A/G | 1.69072e-05 | 0.00290746 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415186 | TCCCAGCCTCTCCCG[A/G]GTCTCCGCCCTGCCT | 25879 |
rs753460762 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421770 | TAATTGTCTTCAAGG[C/T]TTATCCATGTTGTAG | 25879 |
rs753503003 | snp | C/G | 5.03335e-05 | 0.00501639 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415225 | AATGCTCCAGCCCAC[C/G]GACGCGGAAGCGACT | 25879 |
rs753542545 | snp | A/G | | | missense | DCAF13 | GRCh38.p7 | 8:103435762 | GATAAATCTATTCGA[A/G]TCTTTCCTGTAGACA | 25879 |
rs753548168 | snp | C/G | 1.6519e-05 | 0.00287388 | missense | DCAF13 | GRCh38.p7 | 8:103427209 | TATGTTCAATGACCT[C/G]GGGATTTGACAGTAT | 25879 |
rs753553226 | in-del | -/TTTCA | 1.69178e-05 | 0.00290837 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440290 | AGAGAATTCATTTTC[-/TTTCA]TTGTCATAAAGCTGA | 25879 |
rs753634690 | snp | A/G | 1.67203e-05 | 0.00289134 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415452 | AGCAACCGAGATGAA[A/G]GTGAAGATGCTGAGC | 25879 |
rs753675110 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427027 | AGTATAGATAAATAT[A/G]TTTAAAATATTATTC | 25879 |
rs753691850 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441781 | GCCTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTG | 25879 |
rs753746269 | snp | A/C/T | 4.96424e-05 | 0.00498188 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430580 | GCTGCCAGGTCTGGC[A/C/T]TTGAACTGGTGATTG | 25879 |
rs753823513 | snp | A/G | 0.000221951 | 0.0105322 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415524 | ACAGAGAGGTAAGAT[A/G]AGTTGGTAGGGAGAA | 25879 |
rs753853274 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417150 | ACAGTGATTGAAATC[A/G]CATCTGTTAACCACG | 25879 |
rs753905788 | snp | A/C | 8.89814e-05 | 0.00666954 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415078 | CTCTTATGCCCAAGG[A/C]GCGTGAGCGAAGCCG | 25879 |
rs753923613 | snp | A/G | 1.7309e-05 | 0.0029418 | splice-acceptor-variant | DCAF13 | GRCh38.p7 | 8:103440134 | TAATTCGTTTTCTAT[A/G]GGGAGGTATATCATA | 25879 |
rs753941143 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418176 | AGTGTAAATTGCCGC[C/T]AAATCAAGTAGGGAT | 25879 |
rs753949477 | snp | C/T | 1.6955e-05 | 0.00291157 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440295 | ATTCATTTTCTTTCA[C/T]TGTCATAAAGCTGAT | 25879 |
rs753949875 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421148 | AATCTAATTGAATAC[A/T]TTTTTTTTCAAGTTC | 25879 |
rs754232573 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412988 | GTTTTCCTCCTATCA[A/C]CATTTCACAGCTACA | 25879 |
rs754236477 | snp | A/G | 1.67234e-05 | 0.00289161 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415306 | GCGGCGCAGGATCCA[A/G]TTGAGCCAGCAGGCC | 25879 |
rs754276754 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437886 | TTACTGAGCAAACAA[A/G]TAAATTAATAGTGTT | 25879 |
rs754324621 | snp | A/T | 5.00513e-05 | 0.00500231 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415342 | TCCGCGAGTCACGTG[A/T]CTGGAAGTAGTCTGG | 25879 |
rs754373946 | snp | C/T | 1.68892e-05 | 0.00290591 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432642 | AGTGGGAAATTCATC[C/T]ATTCTTCCTTTCTCA | 25879 |
rs754458852 | snp | A/G/T | 8.53052e-05 | 0.0065304 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432627 | AAGAAAAGGAAAGGA[A/G/T]GTGGGAAATTCATCC | 25879 |
rs754525369 | snp | A/G | 2.05772e-05 | 0.00320752 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415564 | TTCCGCAAGTCGTTG[A/G]GTCTAGCCTCGGCTT | 25879 |
rs754661386 | snp | A/G | | | splice-donor-variant | DCAF13 | GRCh38.p7 | 8:103435791 | CAAAAGTCGAAGCAG[A/G]TATGTGCCTACCAGT | 25879 |
rs754711199 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418486 | TGCAGTAGGCTATAG[G/T]CATATCACTGCATTC | 25879 |
rs754719287 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419706 | AACCCAGTTGAAGAG[A/G]GTACTAGGACATATA | 25879 |
rs754722915 | snp | C/T | 5.21889e-05 | 0.00510801 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415098 | GAGCGAAGCCGGAGA[C/T]TCTAGTACTGAGGGG | 25879 |
rs754732343 | in-del | -/TTCA | 1.69026e-05 | 0.00290706 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440291 | GAGAATTCATTTTCT[-/TTCA]TTGTCATAAAGCTGA | 25879 |
rs754803356 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | DCAF13 | GRCh38.p7 | 8:103441525 | TTCAGCATTATCCTC[A/G]TATAAAACGTATAGC | 25879 |
rs754825555 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434711 | AGGAACTTGGTCACA[A/G]TATTGCTGTATTACT | 25879 |
rs754852689 | snp | A/G | | | missense | DCAF13 | GRCh38.p7 | 8:103441609 | TCATGAAAGAAGCTC[A/G]TCGACGAAAGTATGT | 25879 |
rs754856827 | snp | A/G | 4.99297e-05 | 0.00499623 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426124 | AGACGAGGAAGAGCC[A/G]TTACATACAATATTA | 25879 |
rs754919436 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424724 | TAGCGTCTTCAGGAA[C/T]GGGGTGCTCAGGGAC | 25879 |
rs754945687 | snp | G/T | 1.67567e-05 | 0.00289449 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427077 | TGAAAAAAATCCTCT[G/T]AACCTTTTTGCTTTT | 25879 |
rs754947807 | snp | A/C | 1.66346e-05 | 0.00288393 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415362 | AAGTAGTCTGGGAAA[A/C]GCGGAAGTCGCCTGT | 25879 |
rs755062543 | snp | C/G/T | 1.67052e-05 | 0.00289004 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415276 | CTTGCTAACGTTTGC[C/G/T]GGCAAAACTACGGAG | 25879 |
rs755152128 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416106 | ACAAGGGACCAACCA[C/T]GCGTAAGCAGATTGT | 25879 |
rs755173340 | snp | G/T | 2.54696e-05 | 0.00356849 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414927 | GACGCCGACTGGCCC[G/T]GGCCCGTCATAGGCT | 25879 |
rs755186088 | snp | C/T | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103427243 | TAGTGTTAAATTTAA[C/T]CCAATTGAGGTAATG | 25879 |
rs755228849 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440757 | AAAAATAGCAGGTGT[A/T]ATCATTGGCTGGTTA | 25879 |
rs755309968 | snp | C/T | 0.000131843 | 0.00811815 | missense | DCAF13 | GRCh38.p7 | 8:103420999 | TGGAATCTAACTCAG[C/T]GGAATTGTATCCGTA | 25879 |
rs755310481 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424047 | TTTTTGAGATGAAGT[C/G]TCCCTCTGTCGCCCA | 25879 |
rs755314578 | snp | C/T | 0.000560982 | 0.0167385 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103435746 | TGTGTCTGCTAGTTT[C/T]GATAAATCTATTCGA | 25879 |
rs755317031 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439580 | TTTTAGTAGAGACAA[A/G]GTTTCACCATGTTGG | 25879 |
rs755468577 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | DCAF13 | GRCh38.p7 | 8:103421054 | TACGAGGAATATGTA[C/T]TCGCTTTTGTGGGAC | 25879 |
rs755563560 | snp | A/T | 7.37504e-05 | 0.00607205 | missense | DCAF13 | GRCh38.p7 | 8:103442817 | AATCGTATTAAACAC[A/T]GCAAGCCTGGATCTG | 25879 |
rs755636177 | snp | C/G | 1.93939e-05 | 0.00311394 | missense | DCAF13 | GRCh38.p7 | 8:103420459 | CTGGGGCGTGTGATG[C/G]AGAGGCAAGTGTCAA | 25879 |
rs755698556 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | DCAF13 | GRCh38.p7 | 8:103441537 | CTCATATAAAACGTA[C/T]AGCTCGTCATCGACA | 25879 |
rs755726222 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420590 | TCAAGACTAAATTTC[A/G]TTAGGAATACTGTTT | 25879 |
rs755745205 | in-del | -/G | 3.77102e-05 | 0.00434208 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426191 | ATTAACATTCTTTTA[-/G]TTTAAAATTATTTTA | 25879 |
rs755899889 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433880 | GGCATTGTTCCAGTT[A/C]AAGGCAATAAAAGAC | 25879 |
rs755950053 | snp | A/G | 1.65446e-05 | 0.00287612 | missense | DCAF13 | GRCh38.p7 | 8:103427104 | TTTTAAAGACAGTGT[A/G]TACTGGGATTGATCA | 25879 |
rs755956803 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103427201 | TAATCCTATATGTTC[A/G]ATGACCTGGGGATTT | 25879 |
rs756064843 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416280 | TAGGAGATATTATCA[A/G]CATGTGTGTGAGCAT | 25879 |
rs756087392 | snp | C/G | 1.66868e-05 | 0.00288845 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415443 | GGCCGGAAGAGCAAC[C/G]GAGATGAAGGTGAAG | 25879 |
rs756151863 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437560 | GATGTCATTTGGAGG[-/T]TTTTGTAATCACAGT | 25879 |
rs756176285 | snp | C/G | 2.91083e-05 | 0.00381488 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414941 | CTGGCCCGTCATAGG[C/G]TCGGGGCCCGTCGAC | 25879 |
rs756330866 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438092 | ACTTAAGTGACTAAC[C/T]GTTGGATCTGACTGG | 25879 |
rs756417165 | snp | A/C/G | 3.34729e-05 | 0.00409091 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415249 | AGCGACTGCACAGCT[A/C/G]AAGAACCGCCCCTTG | 25879 |
rs756470977 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422212 | CAAGTTTTGAAGGGT[A/G]GCAATGGGAAGGATA | 25879 |
rs756561099 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423123 | AGTGTTGTGCAAGGA[A/G]TTGATTGGCAAGTGG | 25879 |
rs756575758 | snp | C/T | 6.68606e-05 | 0.00578151 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415292 | GGCAAAACTACGGAG[C/T]GGCGCAGGATCCAGT | 25879 |
rs756578074 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435117 | TGGAAACTATTAAAA[C/T]ATAGGGAAATAAATT | 25879 |
rs756595113 | snp | A/G | 4.48964e-05 | 0.00473774 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442927 | TTATTTGTTACTTTT[A/G]ATTTGAGAACTCTAC | 25879 |
rs756650942 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412905 | ATGGAAGCATAAAAA[C/T]TATAGTATGTTACTC | 25879 |
rs756681115 | snp | C/T | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443684 | ATTGATTTCAAGATG[C/T]ACCATTGATGCCAAA | 25879 |
rs756707427 | snp | A/C | 1.64982e-05 | 0.00287208 | missense | DCAF13 | GRCh38.p7 | 8:103430618 | TGTTTTTAGACATTT[A/C]TCTTGGGAAGTTGTG | 25879 |
rs756718921 | in-del | -/A | 6.7761e-05 | 0.0058203 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421130 | ATCAACATAGGTAAG[-/A]ATAATCTAATTGAAT | 25879 |
rs756855598 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant, utr-variant-5-prime | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413442 | GTTTAAATCCCAGAT[C/T]CATCTTTACAAACTT | 25879 |
rs756857669 | snp | C/G | 1.64871e-05 | 0.00287111 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441628 | ACGAAAGTATGTTTT[C/G]AGGCATTTGACTCTA | 25879 |
rs756945539 | snp | A/G/T | 5.66677e-05 | 0.00532271 | missense | DCAF13 | GRCh38.p7 | 8:103442806 | CTAGGGAAGTGAATC[A/G/T]TATTAAACACAGCAA | 25879 |
rs756947557 | snp | G/T | 0.000148543 | 0.00861681 | missense | DCAF13 | GRCh38.p7 | 8:103427141 | GAAAGAAGCTGTTTT[G/T]GCCACATGTGGACAG | 25879 |
rs757035554 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435984 | TGTTGCTTCTAGACT[A/G]CGAATCTGTTCAGCA | 25879 |
rs757072728 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423354 | TACACACACACACGC[A/C]CACAGGAATACTATT | 25879 |
rs757088496 | snp | A/G | 3.34482e-05 | 0.00408937 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415453 | GCAACCGAGATGAAG[A/G]TGAAGATGCTGAGCC | 25879 |
rs757105538 | snp | A/G | 1.93669e-05 | 0.00311176 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415542 | TTGGTAGGGAGAAAG[A/G]GACGGTTTCCGCAAG | 25879 |
rs757150065 | in-del | -/TTAC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434722 | CACAATATTGCTGTA[-/TTAC]TTTTGTCCATTGTTC | 25879 |
rs757179142 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435079 | CGTTGGGAATTTAAT[A/G]AGCATTATATATAAT | 25879 |
rs757182453 | snp | C/T | 3.20682e-05 | 0.00400413 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414949 | TCATAGGCTCGGGGC[C/T]CGTCGACACCACGGC | 25879 |
rs757191177 | snp | A/G | 2.36326e-05 | 0.0034374 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415031 | GGTCGCCCCTTGTGA[A/G]CGCAACCCCACCTCC | 25879 |
rs757199454 | snp | A/G | 1.71443e-05 | 0.00292777 | missense | DCAF13 | GRCh38.p7 | 8:103440140 | GTTTTCTATAGGGAG[A/G]TATATCATACAAAGA | 25879 |
rs757222980 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417154 | TGATTGAAATCACAT[C/T]TGTTAACCACGAAAC | 25879 |
rs757256806 | in-del | -/TTT | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421149 | ATCTAATTGAATACA[-/TTT]TTTTTCAAGTTCATT | 25879 |
rs757289460 | snp | A/C/G | 3.31314e-05 | 0.00406999 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421092 | TTCACTGTAAGTATA[A/C/G]TACCATTAAGTCATT | 25879 |
rs757364367 | snp | G/T | 1.73204e-05 | 0.00294277 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440308 | CATTGTCATAAAGCT[G/T]ATTTCTAATTTTATT | 25879 |
rs757452235 | snp | A/G | 0.000140321 | 0.00837502 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421316 | AAAGTGGAATTAATG[A/G]GAGGTAAGTCTAGAA | 25879 |
rs757482183 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424229 | AGACAGGGTTTCACC[A/G]TGTTAGCCATGATGG | 25879 |
rs757561207 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413031 | TTATTACAAAGTCCT[A/G]CTTCCACTCCTGGAT | 25879 |
rs757596991 | snp | A/T | 1.67267e-05 | 0.0028919 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415307 | CGGCGCAGGATCCAG[A/T]TGAGCCAGCAGGCCG | 25879 |
rs757682864 | snp | C/G | 1.66815e-05 | 0.00288799 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415343 | CCGCGAGTCACGTGA[C/G]TGGAAGTAGTCTGGG | 25879 |
rs757683430 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430828 | CTTAGAACTCTACAT[A/G]ATGATAGTCATGTTC | 25879 |
rs757711096 | snp | C/T | 1.68562e-05 | 0.00290307 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432646 | GGAAATTCATCCATT[C/T]TTCCTTTCTCAGGTT | 25879 |
rs757735149 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441927 | CGCGCCACCATGCGC[G/T]GCTAATTTTTTGTAT | 25879 |
rs757820812 | snp | A/C | 1.65619e-05 | 0.00287762 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420364 | AGTATTTGCAAAACC[A/C]TTCCTTGCTTCGCTG | 25879 |
rs757845018 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441157 | TTTAGGTGCTTTTCT[A/G]TGTTATTGATGCCTA | 25879 |
rs757846848 | snp | A/G | 2.94955e-05 | 0.00384017 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442898 | TTGGTATTCCTAACA[A/G]TCCTGATGTATAATT | 25879 |
rs757849051 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412775 | CCTCTGAGTTCCAAT[C/T]TATACTTGAACTCAC | 25879 |
rs757879506 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435475 | TGTTGAAATTTTTCC[-/T]TTATCCCTCACCTGC | 25879 |
rs757934902 | snp | A/T | 1.65263e-05 | 0.00287452 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430598 | GAACTGGTGATTGTT[A/T]TACTTGTTTTTAGAC | 25879 |
rs757991333 | snp | C/T | 1.84756e-05 | 0.00303932 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427259 | CCAATTGAGGTAATG[C/T]TTTTTTTTAAGTATG | 25879 |
rs758049179 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417291 | CCAAACATTGAATTA[A/G]GCTGAAATTAGAACC | 25879 |
rs758133608 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430251 | CAAAATATTAGCCCG[A/G]TGTGGTGGCGCACCC | 25879 |
rs758162838 | snp | G/T | 2.01177e-05 | 0.0031715 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415553 | AAAGGGACGGTTTCC[G/T]CAAGTCGTTGGGTCT | 25879 |
rs758223306 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418505 | ATCACTGCATTCCAG[C/G]TTGGGTGACAGAATG | 25879 |
rs758251127 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | DCAF13 | GRCh38.p7 | 8:103420323 | CGAGAATATATAAGA[A/G]CTTTAAATGCTACCA | 25879 |
rs758311990 | snp | A/G | 2.28376e-05 | 0.00337909 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440321 | CTGATTTCTAATTTT[A/G]TTAGATATTACATTA | 25879 |
rs758339272 | snp | C/T | 1.67697e-05 | 0.00289561 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426013 | AGTTTTAATTTATAA[C/T]TGTTGTTCCTTACCA | 25879 |
rs758342847 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415087 | CCAAGGCGCGTGAGC[A/G]AAGCCGGAGACTCTA | 25879 |
rs758400351 | snp | G/T | 1.64784e-05 | 0.00287035 | missense | DCAF13 | GRCh38.p7 | 8:103441511 | ATTGAAGGAGAAATT[G/T]CAGCATTATCCTCAT | 25879 |
rs758421829 | snp | A/T | 1.67402e-05 | 0.00289306 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415314 | GGATCCAGTTGAGCC[A/T]GCAGGCCGCCGCTCC | 25879 |
rs758585259 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425574 | CTTAGTAGTTTCTGC[A/G]GTTCATGCAGAAAAG | 25879 |
rs758594833 | snp | G/T | 1.66335e-05 | 0.00288383 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415403 | GGCGGTGGGCGGAAC[G/T]CCTAGCGGACACCTC | 25879 |
rs758697057 | snp | A/C/G | 3.69913e-05 | 0.00430053 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435610 | ATGTGTCAAATATTT[A/C/G]AAAATTCTTTTACAG | 25879 |
rs758718894 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441763 | TTGAAGACTTCTACA[A/G]AAGGCCTTTTCTTTT | 25879 |
rs758756069 | snp | C/T | 3.6931e-05 | 0.00429699 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427322 | TGTTTAGAAAACTTT[C/T]GAATGTATGATAGAA | 25879 |
rs758803229 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420058 | ATACCTAGGGTCTAA[C/T]TGTTTTGCAAGATGT | 25879 |
rs758839320 | in-del | -/G | 1.65012e-05 | 0.00287234 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103420343 | AAATGCTACCAAACT[-/G]GAACGAGTATTTGCA | 25879 |
rs758858822 | snp | A/G | 2.56835e-05 | 0.00358345 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420482 | AGTGTCAATCTAGAT[A/G]ATATTTTCAACTAAA | 25879 |
rs758893088 | snp | C/T | 3.30797e-05 | 0.00406679 | missense | DCAF13 | GRCh38.p7 | 8:103435718 | TGGATTACTCTCCCA[C/T]TGGGAAGGAGTTTGT | 25879 |
rs758905669 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439822 | TTACCTTGGTTGAAC[A/T]TCATATTTTATTTGC | 25879 |
rs758946959 | snp | A/C | 1.64898e-05 | 0.00287135 | missense | DCAF13 | GRCh38.p7 | 8:103420988 | AGGTTAGAATTTGGA[A/C]TCTAACTCAGCGGAA | 25879 |
rs759004885 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420775 | AAAAGTTTTGTAACA[C/G]TTTAGAATCAACAGA | 25879 |
rs759005339 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438971 | CACAGCCTTTCCAAA[G/T]AGGTATGATATTTGA | 25879 |
rs759107382 | snp | A/G | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420424 | GGCAAAGCATCCAGA[A/G]AAGCTGGCTACTGTC | 25879 |
rs759116193 | snp | A/G | 6.65093e-05 | 0.0057663 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415378 | GCGGAAGTCGCCTGT[A/G]GGAGGAGGTGGCGGT | 25879 |
rs759116286 | snp | C/G | 0.000153585 | 0.00876178 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414760 | AGTGAGAGGATGCAG[C/G]CCGGTGTCTGGGCGG | 25879 |
rs759157574 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431668 | TATTAATAACTATCT[C/T]GCAGCACTTCGCTGA | 25879 |
rs759160467 | snp | A/T | 0.000102951 | 0.00717391 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103435662 | TGCACTGGACACTCC[A/T]GTAATGGTCCATATG | 25879 |
rs759172485 | snp | A/G | 1.69327e-05 | 0.00290965 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414785 | GGGCGGGCTCTTACC[A/G]GCGAAGCGGATCTTC | 25879 |
rs759188474 | snp | A/G | 1.70659e-05 | 0.00292107 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432771 | TTTAAAAACTTGTGT[A/G]TTTCTATCATGAATG | 25879 |
rs759245083 | snp | C/G | 1.65817e-05 | 0.00287933 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420958 | TCACTGAAATTTCCT[C/G]GTATGCCTTATCATA | 25879 |
rs759281100 | snp | C/G | 1.78701e-05 | 0.0029891 | missense | DCAF13 | GRCh38.p7 | 8:103420440 | AAGCTGGCTACTGTC[C/G]TTTCTGGGGCGTGTG | 25879 |
rs759482900 | snp | C/T | 1.69335e-05 | 0.00290972 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415179 | GGGGAGGTCCCAGCC[C/T]CTCCCGAGTCTCCGC | 25879 |
rs759522627 | snp | G/T | 3.89067e-05 | 0.00441042 | missense | DCAF13 | GRCh38.p7 | 8:103442852 | ACTTGTGTCAGAGAA[G/T]AAGAAACACGTAGTG | 25879 |
rs759559334 | snp | C/T | 2.68244e-05 | 0.00366217 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442768 | AGTTCCCATAACTTG[C/T]TTATATTTTGTATAT | 25879 |
rs759571077 | snp | C/T | 3.36134e-05 | 0.00409946 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415215 | CTCGCCCACAAATGC[C/T]CCAGCCCACGGACGC | 25879 |
rs759593523 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432180 | GTGGGAGGTCCCTGA[A/G]TGGCAAAACATCCTA | 25879 |
rs759596988 | snp | A/G | 1.65105e-05 | 0.00287315 | missense | DCAF13 | GRCh38.p7 | 8:103427195 | AAGAACTAATCCTAT[A/G]TGTTCAATGACCTGG | 25879 |
rs759718195 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | DCAF13 | GRCh38.p7 | 8:103441543 | TAAAACGTATAGCTC[A/G]TCATCGACATCTACC | 25879 |
rs759774876 | snp | C/T | 3.51265e-05 | 0.00419071 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415501 | GTCCGCGAAACCAAG[C/T]TGGACTTACAGAGAG | 25879 |
rs759805204 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416820 | CCATCTATAAAGATT[C/T]ATTTTTGCCTACATG | 25879 |
rs759985775 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413634 | TTACTTGTCAATAAC[-/AT]AATTATTTGTGCATG | 25879 |
rs759996685 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442281 | AAGAGATTTTGTGTA[-/T]TTTTCCAAGTTAAAG | 25879 |
rs760009356 | snp | A/T | 0.000241546 | 0.010987 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421252 | TTCTTTATATAATTC[A/T]GCCTTCCCCATAACT | 25879 |
rs760168265 | snp | C/T | 3.38061e-05 | 0.00411119 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441444 | TAAGATACCAAAATG[C/T]GTATTTTCAGCTTAC | 25879 |
rs760182857 | snp | A/T | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443735 | TTGATATTAAATGGC[A/T]TAGTATATGGATATA | 25879 |
rs760192000 | snp | A/T | 1.672e-05 | 0.00289132 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103435692 | GGATCATGTATCTGC[A/T]GTGCTTGATGTGGAT | 25879 |
rs760205116 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436744 | GAATTATGGTTTACA[A/G]AGAGCTGTTATACAC | 25879 |
rs760233515 | snp | A/T | 2.03432e-05 | 0.00318923 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414892 | CGTGGCGGAATACCG[A/T]GCTCCACGCCGACGA | 25879 |
rs760281498 | snp | C/T | 1.65351e-05 | 0.00287528 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420966 | ATTTCCTGGTATGCC[C/T]TATCATAGGTTAGAA | 25879 |
rs760294858 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435557 | TTCTTGTTTTCAGTG[A/G]TATCTTTTAGTACTG | 25879 |
rs760383267 | snp | C/G | 1.67992e-05 | 0.00289816 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415219 | CCCACAAATGCTCCA[C/G]CCCACGGACGCGGAA | 25879 |
rs760550577 | snp | A/G | 1.94668e-05 | 0.00311978 | missense | DCAF13 | GRCh38.p7 | 8:103442799 | TTTATTTCTAGGGAA[A/G]TGAATCGTATTAAAC | 25879 |
rs760605028 | snp | C/T | 3.3423e-05 | 0.00408783 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415266 | AGAACCGCCCCTTGC[C/T]AACGTTTGCCGGCAA | 25879 |
rs760640368 | snp | A/G | 2.21899e-05 | 0.00333084 | missense | DCAF13 | GRCh38.p7 | 8:103442868 | AAGAAACACGTAGTG[A/G]CAGTTGTAAAATAAT | 25879 |
rs760659295 | snp | A/C | 1.65523e-05 | 0.00287678 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430717 | TTTGACTTTTGCTTT[A/C]TACAGTTGGCATTAT | 25879 |
rs760685505 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428960 | GGTAAAAGTAAATGG[G/T]GTGTGTGTCTCTTAT | 25879 |
rs760727387 | in-del | -/CGC | 1.64781e-05 | 0.00287033 | utr-variant-5-prime, cds-indel, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414837 | CAAGGTTGGATAAGA[-/CGC]CGCCGCCGCTCACGC | 25879 |
rs760741200 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440449 | TTGCTTCATTCTGAT[A/C]TATTATTGTAGACAC | 25879 |
rs760754789 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428270 | CACACTTTCTAGAGA[C/T]GCTACAGGTCTAGAA | 25879 |
rs760825140 | snp | A/G | 3.02604e-05 | 0.00388964 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415016 | CGCCACCGTGGCGAC[A/G]GTCGCCCCTTGTGAG | 25879 |
rs760844804 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429893 | AAAAGCCATAAAATT[G/T]TTCATACCTTTTGAT | 25879 |
rs760874486 | in-del | -/GCT | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414680 | AACGCGGACAGCAAC[-/GCT]CCCTTCAACGCTCCT | 25879 |
rs760880662 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434264 | AACTAACTCTATATC[A/G]TAGTTTCAGCATCTG | 25879 |
rs760971020 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437687 | TGTGGTTTGTTTCCT[A/G]TCATTATAAACATCA | 25879 |
rs760999576 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439736 | AAGGGGAAAAAAAGT[A/G]TGTTGACCTGAATTG | 25879 |
rs761157408 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435289 | ATAGTATGGTGAAAA[A/G]GGTTTTTTAAAAAAT | 25879 |
rs761206266 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424111 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 25879 |
rs761225553 | snp | A/G | 1.65351e-05 | 0.00287528 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426088 | TGTGAAGCAGTGGAA[A/G]ATGGATGGGCCAGGC | 25879 |
rs761301834 | snp | C/T | 1.64779e-05 | 0.00287031 | stop-gained | DCAF13 | GRCh38.p7 | 8:103421041 | CATGAAGGCTTTGTA[C/T]GAGGAATATGTACTC | 25879 |
rs761315213 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413720 | TACTCCATAATTTTC[G/T]ATGATTTTCCTTCAT | 25879 |
rs761369421 | snp | A/G | 1.65042e-05 | 0.0028726 | missense | DCAF13 | GRCh38.p7 | 8:103440203 | TCTGACAGCAAGTAT[A/G]TTATGTGTGGATCTG | 25879 |
rs761385547 | snp | A/G | 3.37484e-05 | 0.00410769 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421127 | TTGATCAACATAGGT[A/G]AGAATAATCTAATTG | 25879 |
rs761389780 | snp | A/G | 5.03149e-05 | 0.00501547 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415229 | CTCCAGCCCACGGAC[A/G]CGGAAGCGACTGCAC | 25879 |
rs761436430 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440894 | AAGTTTAAGAAGGAA[A/G]GGGTAAGTGTGAATT | 25879 |
rs761475099 | snp | C/G | 1.67077e-05 | 0.00289026 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415270 | CCGCCCCTTGCTAAC[C/G]TTTGCCGGCAAAACT | 25879 |
rs761509039 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413266 | CACCTCTTCTGCTCC[C/T]AGATAAAATGCTACT | 25879 |
rs761547809 | snp | A/G | | | missense | DCAF13 | GRCh38.p7 | 8:103440234 | ATGAAATGAACATTC[A/G]CCTGTGGAAAGCTAA | 25879 |
rs761622194 | snp | C/T | 2.5107e-05 | 0.003543 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442884 | CAGTTGTAAAATAAT[C/T]GGTATTCCTAACAAT | 25879 |
rs761806045 | snp | C/T | 3.31741e-05 | 0.00407259 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430727 | GCTTTATACAGTTGG[C/T]ATTATATATTTCTCT | 25879 |
rs761862300 | snp | A/G | 9.89446e-05 | 0.00703296 | missense | DCAF13 | GRCh38.p7 | 8:103420309 | CTTTTGAGGTCCCAC[A/G]AGAATATATAAGAGC | 25879 |
rs761894129 | snp | A/G | 1.66674e-05 | 0.00288676 | missense | DCAF13 | GRCh38.p7 | 8:103432719 | GAAGCTTTCATTTTT[A/G]CAGCAGCAAATGAAG | 25879 |
rs761897743 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418220 | CCCAAGTATAAGATA[A/C]TGAAGACCCAAACTG | 25879 |
rs761950146 | snp | G/T | 1.76646e-05 | 0.00297186 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415082 | TATGCCCAAGGCGCG[G/T]GAGCGAAGCCGGAGA | 25879 |
rs761994850 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432570 | CTGAGTACTTTACAC[A/G]TAATAGGTGTTTATG | 25879 |
rs762246113 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425478 | TTTACTAACATTATG[A/G]AAATAGTTTTGACTG | 25879 |
rs762335747 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415124 | AGGGGGCAAGAACGG[C/G]GCACAGACACTACGT | 25879 |
rs762435482 | snp | C/G/T | 3.33029e-05 | 0.00408051 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415418 | TCCTAGCGGACACCT[C/G/T]GTGGAGTCCGGCCGG | 25879 |
rs762519951 | snp | C/G/T | 4.96129e-05 | 0.0049804 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103426073 | TGGTGATGACAAAAC[C/G/T]GTGAAGCAGTGGAAA | 25879 |
rs762556235 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423976 | GTGTTGGGATTACAG[A/G]CATGAGTCACCATGC | 25879 |
rs762615857 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413410 | GTGCCAGAGGGTTCC[A/C]GAGTTAGATTACCTG | 25879 |
rs762639048 | snp | C/G | 1.70249e-05 | 0.00291756 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432767 | CTCTTTTAAAAACTT[C/G]TGTATTTCTATCATG | 25879 |
rs762667636 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431544 | TTCCAAAGTACCACT[A/T]ATATGATTTCACTCA | 25879 |
rs762674539 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439150 | GCTGGGACTACAGGC[A/G]CCTGCCACCATGCCT | 25879 |
rs762711361 | snp | C/T | 5.09057e-05 | 0.00504482 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414777 | CGGTGTCTGGGCGGG[C/T]TCTTACCGGCGAAGC | 25879 |
rs762764765 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437096 | CATTTCATCATTTCT[G/T]TTGTAGAGCTTCTGC | 25879 |
rs762913618 | snp | C/T | 5.09057e-05 | 0.00504482 | missense | DCAF13 | GRCh38.p7 | 8:103420411 | GAGTCAATTGCTTGG[C/T]AAAGCATCCAGAGAA | 25879 |
rs762994652 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103420316 | GGTCCCACGAGAATA[C/T]ATAAGAGCTTTAAAT | 25879 |
rs763005420 | snp | C/T | 1.68046e-05 | 0.00289862 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420933 | ATCCTGAACATTTTA[C/T]ATTTATAGTTCACTG | 25879 |
rs763038882 | snp | C/T | 0.000724614 | 0.0190206 | missense | DCAF13 | GRCh38.p7 | 8:103441590 | CAGATTCAGGAACAG[C/T]GCATCATGAAAGAAG | 25879 |
rs763042484 | snp | A/G | 3.41204e-05 | 0.00413026 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427064 | TTTGAATTAGTAATG[A/G]AAAAAATCCTCTTAA | 25879 |
rs763067156 | snp | C/T | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443143 | TGTTTTTATTACAGA[C/T]ATACTTACTTTCTCT | 25879 |
rs763090757 | snp | A/C/T | 6.77305e-05 | 0.00581905 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415177 | GAGGGGAGGTCCCAG[A/C/T]CTCTCCCGAGTCTCC | 25879 |
rs763165621 | in-del | -/G | 6.83387e-05 | 0.00584506 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432624 | GAAAAGAAAAGGAAA[-/G]GAAGTGGGAAATTCA | 25879 |
rs763185691 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426333 | CTAAAGAATTTTAAC[-/A]AGTTTTTTTTTTTTT | 25879 |
rs763209111 | snp | A/C/G | 8.25206e-05 | 0.00642298 | missense | DCAF13 | GRCh38.p7 | 8:103427176 | TAGACATTTGGGATG[A/C/G]ACAAAGAACTAATCC | 25879 |
rs763306761 | snp | C/G | 1.69464e-05 | 0.00291083 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415477 | CTGAGCCGGAATCCG[C/G]ACAATTATGTCCGCG | 25879 |
rs763367767 | snp | C/G | 1.66579e-05 | 0.00288595 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415426 | GACACCTCGTGGAGT[C/G]CGGCCGGAAGAGCAA | 25879 |
rs763398540 | snp | A/C | 0.000153245 | 0.00875209 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414989 | CGCGGAGGTGGGACG[A/C]GATGCAGTGGCCGCC | 25879 |
rs763459527 | snp | A/G | 2.30854e-05 | 0.00339737 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414912 | CACGCCGACGACCCG[A/G]ACGCCGACTGGCCCT | 25879 |
rs763466637 | in-del | -/GAG | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414594 | CCCTCTCTTAGTCTT[-/GAG]GAGCGGGGAAGATCG | 25879 |
rs763529960 | snp | G/T | 3.32331e-05 | 0.0040762 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103435704 | TGCAGTGCTTGATGT[G/T]GATTACTCTCCCACT | 25879 |
rs763601552 | snp | A/G | | | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103442882 | GGCAGTTGTAAAATA[A/G]TTGGTATTCCTAACA | 25879 |
rs763709416 | snp | C/G | 3.29544e-05 | 0.00405908 | missense | DCAF13 | GRCh38.p7 | 8:103421033 | TACAAGCACATGAAG[C/G]CTTTGTACGAGGAAT | 25879 |
rs763935874 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430567 | ATGGATGTGGTTTGC[C/T]GCCAGGTCTGGCTTT | 25879 |
rs763941283 | snp | A/C/T | 3.79638e-05 | 0.00435669 | missense | DCAF13 | GRCh38.p7 | 8:103442805 | TCTAGGGAAGTGAAT[A/C/T]GTATTAAACACAGCA | 25879 |
rs763967066 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437361 | GACAAAAGAATGAAA[C/T]GAGAACAAAGAAAAA | 25879 |
rs763998434 | snp | A/G | 3.30256e-05 | 0.00406346 | missense | DCAF13 | GRCh38.p7 | 8:103427202 | AATCCTATATGTTCA[A/G]TGACCTGGGGATTTG | 25879 |
rs764006962 | in-del | -/AA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433896 | AAGGCAATAAAAGAC[-/AA]GAGTAATACAGCATT | 25879 |
rs764023488 | snp | G/T | 3.69263e-05 | 0.00429672 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415523 | TACAGAGAGGTAAGA[G/T]AAGTTGGTAGGGAGA | 25879 |
rs764168183 | in-del | -/AGC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429301 | AGCAGCCATTAAGAT[-/AGC]AGGCTTTCAGAAAGA | 25879 |
rs764280139 | snp | C/G | 1.78153e-05 | 0.00298452 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415077 | ACTCTTATGCCCAAG[C/G]CGCGTGAGCGAAGCC | 25879 |
rs764300108 | snp | A/G | 1.65509e-05 | 0.00287666 | missense | DCAF13 | GRCh38.p7 | 8:103441465 | TTCAGCTTACATCAC[A/G]AGAAAAAGCAGCCAA | 25879 |
rs764408338 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424135 | GCCATTCTCTTGCCT[C/G]AGTCTCCCCAGTAGC | 25879 |
rs764420462 | snp | A/G | | | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103443302 | TAGAATAATGATGTC[A/G]ATTTTTTACAACTGA | 25879 |
rs764577285 | snp | C/T | 3.30857e-05 | 0.00406716 | missense | DCAF13 | GRCh38.p7 | 8:103426098 | TGGAAAATGGATGGG[C/T]CAGGCTATGGAGACG | 25879 |
rs764578714 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414677 | GCCAACGCGGACAGC[-/AA]CGCTCCCTTCAACGC | 25879 |
rs764620099 | in-del | -/AA | 1.86837e-05 | 0.00305639 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435602 | CTAGAAATATGTGTC[-/AA]ATATTTAAAAATTCT | 25879 |
rs764640465 | in-del | -/G | 1.67657e-05 | 0.00289527 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103420394 | GATGGTCACCGTGAT[-/G]GGAGTCAATTGCTTG | 25879 |
rs764651330 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425231 | GTTTTGTATGTATGC[A/G]GTTATACAGTACCAC | 25879 |
rs764680089 | snp | A/G | 0.000117295 | 0.00765727 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421243 | TTACTAGTTTTCTTT[A/G]TATAATTCAGCCTTC | 25879 |
rs764706100 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103417237 | ACAGTGCGAAAGTGA[G/T]TACTGCTTGAATTTT | 25879 |
rs764752514 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421908 | TTTTGGCTATTGTGA[A/G]TAGTGTTGCCGTGAC | 25879 |
rs764756082 | snp | A/G | 1.67666e-05 | 0.00289534 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415231 | CCAGCCCACGGACGC[A/G]GAAGCGACTGCACAG | 25879 |
rs764759291 | snp | A/G | 1.66247e-05 | 0.00288307 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415382 | AAGTCGCCTGTGGGA[A/G]GAGGTGGCGGTGGGC | 25879 |
rs764780251 | snp | C/G | 2.73437e-05 | 0.00369745 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442892 | AAATAATTGGTATTC[C/G]TAACAATCCTGATGT | 25879 |
rs764845323 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436999 | TTGTCAGCAGATAAT[G/T]ATCTTCATCACTGTT | 25879 |
rs764846524 | snp | G/T | 3.34107e-05 | 0.00408708 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415271 | CGCCCCTTGCTAACG[G/T]TTGCCGGCAAAACTA | 25879 |
rs764896429 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428542 | TATATCTTTCTCACT[C/T]CATCCTCCATCTTCC | 25879 |
rs765059789 | snp | C/G | 1.65479e-05 | 0.0028764 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430583 | GCCAGGTCTGGCTTT[C/G]AACTGGTGATTGTTA | 25879 |
rs765124684 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430195 | CAGGAGTTTGATACC[A/C]GCCTGGGCAACATGG | 25879 |
rs765146546 | snp | A/G | 1.76139e-05 | 0.00296759 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415085 | GCCCAAGGCGCGTGA[A/G]CGAAGCCGGAGACTC | 25879 |
rs765149441 | snp | G/T | 1.96207e-05 | 0.00313209 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415546 | TAGGGAGAAAGGGAC[G/T]GTTTCCGCAAGTCGT | 25879 |
rs765149525 | snp | A/G | 1.65872e-05 | 0.00287981 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430731 | TATACAGTTGGCATT[A/G]TATATTTCTCTGTAA | 25879 |
rs765259698 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418335 | AGTAGCCTGGGCATC[A/G]TAAGGAGACCCCCGT | 25879 |
rs765345938 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419411 | AAGGTTTTTGGAACA[G/T]CGCCTGGCACTTGAA | 25879 |
rs765398033 | in-del | -/G | 1.67705e-05 | 0.00289568 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415231 | CCAGCCCACGGACGC[-/G]GAAGCGACTGCACAG | 25879 |
rs765410014 | snp | A/G | 1.65026e-05 | 0.00287246 | missense | DCAF13 | GRCh38.p7 | 8:103441479 | CGAGAAAAAGCAGCC[A/G]AGGATTATAACCAGA | 25879 |
rs765438024 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | DCAF13 | GRCh38.p7 | 8:103441581 | ATCTATAGCCAGATT[C/G]AGGAACAGCGCATCA | 25879 |
rs765465944 | snp | A/C | 3.77102e-05 | 0.00434208 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426191 | TATTAACATTCTTTT[A/C]TTTAAAATTATTTTA | 25879 |
rs765496368 | snp | A/G | 1.65567e-05 | 0.00287716 | missense | DCAF13 | GRCh38.p7 | 8:103426107 | GATGGGCCAGGCTAT[A/G]GAGACGAGGAAGAGC | 25879 |
rs765496476 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424252 | CATGATGGTCTCGAT[C/G]TCCTGACCTAGTGAT | 25879 |
rs765503657 | snp | A/G | 6.59011e-05 | 0.00573988 | missense | DCAF13 | GRCh38.p7 | 8:103441602 | CAGCGCATCATGAAA[A/G]AAGCTCGTCGACGAA | 25879 |
rs765532854 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425483 | TAACATTATGAAAAT[A/T]GTTTTGACTGTGTGG | 25879 |
rs765595519 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440776 | ATTGGCTGGTTACCT[A/C]CAGGATAGGGGATTA | 25879 |
rs765639695 | snp | A/G | 6.67022e-05 | 0.00577466 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415346 | CGAGTCACGTGACTG[A/G]AAGTAGTCTGGGAAA | 25879 |
rs765673482 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413358 | TTCAAACCATTGTAT[A/C]ACAGGTACTTATAGA | 25879 |
rs765729504 | snp | A/G | 6.65048e-05 | 0.00576611 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415391 | GTGGGAGGAGGTGGC[A/G]GTGGGCGGAACTCCT | 25879 |
rs765808271 | snp | C/T | 1.67435e-05 | 0.00289335 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415326 | GCCAGCAGGCCGCCG[C/T]TCCGCGAGTCACGTG | 25879 |
rs765817450 | snp | C/T | 1.68895e-05 | 0.00290593 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414796 | TACCGGCGAAGCGGA[C/T]CTTCACGAGGTCGAG | 25879 |
rs765819684 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433167 | AGTTGGCTGATGTTT[C/G]ATGTAGGTCTTATAA | 25879 |
rs765828608 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425592 | CATGCAGAAAAGGAC[-/T]TTTATCTATTTCAAT | 25879 |
rs765852245 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440562 | TTGTGTTTTCCTTGA[C/G]GTAGGGACAGAAGAT | 25879 |
rs765910763 | snp | A/G | 0.000110797 | 0.0074422 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414903 | ACCGTGCTCCACGCC[A/G]ACGACCCGGACGCCG | 25879 |
rs766020176 | snp | A/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant, utr-variant-5-prime | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413439 | TGGGTTTAAATCCCA[A/G]ATCCATCTTTACAAA | 25879 |
rs766072456 | snp | A/C | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443778 | CCTCCCAAATACTTA[A/C]AATCATCTCTAGATT | 25879 |
rs766137900 | snp | C/T | 5.11104e-05 | 0.00505496 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432768 | TCTTTTAAAAACTTG[C/T]GTATTTCTATCATGA | 25879 |
rs766176545 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434621 | TATCTTTGGGGAGAT[A/G]CTTTGAAACTATGTA | 25879 |
rs766215478 | snp | A/G | 1.64933e-05 | 0.00287165 | missense | DCAF13 | GRCh38.p7 | 8:103420330 | ATATAAGAGCTTTAA[A/G]TGCTACCAAACTGGA | 25879 |
rs766234391 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419573 | TGTTCCCTGCCCTAC[A/C]GGAAGCTTAGAGTTC | 25879 |
rs766294351 | snp | A/T | 1.64776e-05 | 0.00287028 | missense | DCAF13 | GRCh38.p7 | 8:103441519 | AGAAATTTCAGCATT[A/T]TCCTCATATAAAACG | 25879 |
rs766307601 | snp | A/G | 1.69913e-05 | 0.00291468 | missense | DCAF13 | GRCh38.p7 | 8:103420413 | GTCAATTGCTTGGCA[A/G]AGCATCCAGAGAAGC | 25879 |
rs766382243 | snp | A/G | 0.000115311 | 0.00759224 | missense | DCAF13 | GRCh38.p7 | 8:103441591 | AGATTCAGGAACAGC[A/G]CATCATGAAAGAAGC | 25879 |
rs766393233 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415133 | GAACGGGGCACAGAC[A/G]CTACGTCACGCCGGC | 25879 |
rs766465691 | snp | A/C | 1.68383e-05 | 0.00290153 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427073 | GTAATGAAAAAAATC[A/C]TCTTAACCTTTTTGC | 25879 |
rs766544817 | in-del | -/CTGGCC | 0.000120185 | 0.00775101 | utr-variant-5-prime, cds-indel, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414919 | CGACCCGGACGCCGA[-/CTGGCC]CTGGCCCTGGCCCGT | 25879 |
rs766563782 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440464 | CTATTATTGTAGACA[C/T]TGTACATTCAAATTG | 25879 |
rs766564702 | snp | C/T | 1.66601e-05 | 0.00288614 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415427 | ACACCTCGTGGAGTC[C/T]GGCCGGAAGAGCAAC | 25879 |
rs766582709 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426543 | AGAAATGAAGAAATT[A/T]AATAGTATTATGCAT | 25879 |
rs766589820 | snp | C/G | 1.66338e-05 | 0.00288386 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415404 | GCGGTGGGCGGAACT[C/G]CTAGCGGACACCTCG | 25879 |
rs766591219 | in-del | -/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414680 | ACGCGGACAGCAACG[-/C]CTCCCTTCAACGCTC | 25879 |
rs766656853 | snp | A/G | 2.48623e-05 | 0.0035257 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414923 | CCCGGACGCCGACTG[A/G]CCCTGGCCCGTCATA | 25879 |
rs766681889 | snp | C/G | 1.68992e-05 | 0.00290677 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414808 | GGATCTTCACGAGGT[C/G]GAGCGGATGCAGCGC | 25879 |
rs766706100 | snp | G/T | 1.65091e-05 | 0.00287303 | missense | DCAF13 | GRCh38.p7 | 8:103435735 | GGGAAGGAGTTTGTG[G/T]CTGCTAGTTTCGATA | 25879 |
rs766733860 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432922 | GAAAAGTATTTATTT[C/T]GTCAGTATTTAGAAT | 25879 |
rs766944140 | snp | A/G | 1.69132e-05 | 0.00290797 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414790 | GGCTCTTACCGGCGA[A/G]GCGGATCTTCACGAG | 25879 |
rs767036356 | snp | C/T | 1.71141e-05 | 0.00292519 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432775 | AAAACTTGTGTATTT[C/T]TATCATGAATGGCTT | 25879 |
rs767063339 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431725 | TAGCAGAATGCTGAC[A/C]TGAGGTACTAGTTTA | 25879 |
rs767072080 | snp | G/T | 0.000102367 | 0.00715354 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415025 | GGCGACGGTCGCCCC[G/T]TGTGAGCGCAACCCC | 25879 |
rs767118887 | snp | C/T | 5.01475e-05 | 0.00500712 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415261 | GCTAAAGAACCGCCC[C/T]TTGCTAACGTTTGCC | 25879 |
rs767153044 | snp | A/G | 1.69689e-05 | 0.00291275 | missense | DCAF13 | GRCh38.p7 | 8:103435673 | CTCCTGTAATGGTCC[A/G]TATGGATCATGTATC | 25879 |
rs767154981 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419865 | AATAGAAAAATTAGC[C/T]GGGCGTGGTGGCATG | 25879 |
rs767172264 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441197 | CAACTCAGTGATCCA[C/T]GTGGCCCTACTCCTT | 25879 |
rs767286775 | snp | A/G | 1.65616e-05 | 0.00287759 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420961 | CTGAAATTTCCTGGT[A/G]TGCCTTATCATAGGT | 25879 |
rs767397756 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439227 | CGATCTCCTGACCTC[C/G]TGATCCACCTACTGC | 25879 |
rs767442115 | snp | C/T | 3.38438e-05 | 0.00411349 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440292 | AGAATTCATTTTCTT[C/T]CATTGTCATAAAGCT | 25879 |
rs767487448 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436725 | ATACAGCCCCCTGTA[-/T]AGTGAATTATGGTTT | 25879 |
rs767507574 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423413 | ACTTGCAGCATACAT[G/T]AATGAACCTGGAGGA | 25879 |
rs767614845 | snp | G/T | 1.66654e-05 | 0.00288659 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415429 | ACCTCGTGGAGTCCG[G/T]CCGGAAGAGCAACCG | 25879 |
rs767665326 | snp | A/G | 0.000206753 | 0.0101653 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427329 | AAAACTTTTGAATGT[A/G]TGATAGAAACTTCTG | 25879 |
rs767702852 | snp | C/T | 5.33025e-05 | 0.00516221 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415506 | CGAAACCAAGTTGGA[C/T]TTACAGAGAGGTAAG | 25879 |
rs767731576 | in-del | -/TGTGA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436915 | CTTTGCTCTTTTACT[-/TGTGA]TATTTAAGTCTTTTT | 25879 |
rs767769166 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416871 | GATCTATCTTGTTGG[C/G]GTTTTTAAACTTCTG | 25879 |
rs767788695 | snp | A/G | 3.35205e-05 | 0.00409379 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415008 | GCAGTGGCCGCCACC[A/G]TGGCGACGGTCGCCC | 25879 |
rs767792186 | snp | G/T | 1.64808e-05 | 0.00287057 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421055 | ACGAGGAATATGTAC[G/T]CGCTTTTGTGGGACT | 25879 |
rs767858902 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434922 | TATAAATTAGTGCAA[C/T]TTTGTTGGCAGTGAT | 25879 |
rs767924592 | snp | A/G | 1.76586e-05 | 0.00297136 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440115 | AATCCAAAGGGTTTT[A/G]ACTTAATTCGTTTTC | 25879 |
rs767935960 | in-del | -/TG | 1.65685e-05 | 0.00287819 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103440173 | ATGCAACATGTTATC[-/TG]TGTAAAATGGACTTC | 25879 |
rs767955058 | snp | A/G | | | downstream-variant-500B | DCAF13 | GRCh38.p7 | 8:103443658 | CAGTCATCACTCTGT[A/G]TCTGTGGGAGATTGA | 25879 |
rs767980913 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416690 | TCATGATTATTATTT[G/T]GGTTAATAGTCTTTC | 25879 |
rs768014694 | snp | A/G | 1.65389e-05 | 0.00287562 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103440238 | AATGAACATTCGCCT[A/G]TGGAAAGCTAATGCT | 25879 |
rs768037483 | snp | A/G | 0.000519009 | 0.0161008 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421274 | CCCATAACTTAACAT[A/G]ATTAAACTAATATTC | 25879 |
rs768133226 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423067 | CATTCAGTTACTTTT[C/G]ACTAGAGGGGTGCAG | 25879 |
rs768245244 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428284 | ACGCTACAGGTCTAG[A/G]ATAGGTTGGCAAACT | 25879 |
rs768261315 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441339 | AGAATTACATTGGCA[A/G]TTTTGGTTGCATATC | 25879 |
rs768292692 | snp | A/G | 7.74473e-05 | 0.00622235 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414981 | CCCAGGGCCGCGGAG[A/G]TGGGACGCGATGCAG | 25879 |
rs768327742 | snp | A/C | | | missense | DCAF13 | GRCh38.p7 | 8:103440185 | ATCTGTGTAAAATGG[A/C]CTTCTGACAGCAAGT | 25879 |
rs768357734 | snp | A/G | 3.35166e-05 | 0.00409355 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421119 | CATTAAATTTGATCA[A/G]CATAGGTAAGAATAA | 25879 |
rs768360086 | in-del | -/TTAC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440344 | TTACATTATGAAAAT[-/TTAC]TTTTAGGTATTTTTG | 25879 |
rs768382507 | snp | A/T | 1.88283e-05 | 0.00306819 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415054 | CCACCTCCGGGACCA[A/T]CGAGAGGACTCTTAT | 25879 |
rs768436348 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422807 | TGAGTTATAAAATGT[A/G]GGTTGCAATCCAGGT | 25879 |
rs768441410 | snp | C/T | 5.00513e-05 | 0.00500231 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426033 | GTTCCTTACCATCAT[C/T]ATAATAAAACAAATA | 25879 |
rs768448826 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434051 | CCTGAAACAAAGAGC[A/T]TATCCCTTATAATAA | 25879 |
rs768529816 | snp | A/G | 0.000620415 | 0.0176018 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415317 | TCCAGTTGAGCCAGC[A/G]GGCCGCCGCTCCGCG | 25879 |
rs768543989 | in-del | -/A | 3.41974e-05 | 0.00413492 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414748 | TTCGGGCTGACAGTG[-/A]AGAGGATGCAGCCCG | 25879 |
rs768598327 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436852 | ATTTTTCTCAAAAAA[C/T]TATGATAATTGGATG | 25879 |
rs768604116 | snp | A/C | 1.70592e-05 | 0.0029205 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414762 | TGAGAGGATGCAGCC[A/C]GGTGTCTGGGCGGGC | 25879 |
rs768646380 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414368 | TCCCAACCATTCGCT[A/G]AAGATTACGCCCTAT | 25879 |
rs768651600 | snp | A/G | 3.33128e-05 | 0.00408109 | missense | DCAF13 | GRCh38.p7 | 8:103432701 | ATCTGTTGGAACCCT[A/G]TGGAAGCTTTCATTT | 25879 |
rs768726446 | snp | A/G | 6.62449e-05 | 0.00575483 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430721 | ACTTTTGCTTTATAC[A/G]GTTGGCATTATATAT | 25879 |
rs768741309 | snp | A/G/T | 6.69124e-05 | 0.0057838 | missense | DCAF13 | GRCh38.p7 | 8:103420390 | CGCTGGATGGTCACC[A/G/T]TGATGGAGTCAATTG | 25879 |
rs768892969 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431216 | CTAAAGTAGTAATTT[A/C]AGGACTTACATATCA | 25879 |
rs768983000 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432355 | CTCACCATTAATTTT[A/G]CCCCTAATTTGATAC | 25879 |
rs769010877 | snp | C/T | 1.65e-05 | 0.00287224 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441642 | TGAGGCATTTGACTC[C/T]ATTACCCTTTTCTGA | 25879 |
rs769036442 | in-del | -/AATAATATTCA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431009 | GTTACTTAACAGTGT[-/AATAATATTCA]AATAATATTCAATAA | 25879 |
rs769072966 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420119 | AAAGATTTCTGAACA[A/G]CAGGTCTTCTACTTT | 25879 |
rs769196331 | in-del | -/AA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424286 | CCGCCTCAGCCTCTG[-/AA]AAAGTGCTGGGATTA | 25879 |
rs769197042 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439984 | ACGGAACCTTATTAG[C/T]TGGGTTCAATAAAAA | 25879 |
rs769238674 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419733 | TATAAAAGGGAGGCC[A/G]GGCACGGTGGCTCAT | 25879 |
rs769246848 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436492 | GCACATAGAGTGTGA[C/T]TCTAATATTTAAGAT | 25879 |
rs769256642 | snp | A/T | 1.93373e-05 | 0.00310939 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426176 | GACTAATAGCTTGCC[A/T]ATTAACATTCTTTTA | 25879 |
rs769271546 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425131 | TCTTCCCTTAGATAA[A/G]GATATCTTTGTTAAT | 25879 |
rs769347024 | snp | A/C | 1.65037e-05 | 0.00287256 | missense | DCAF13 | GRCh38.p7 | 8:103427158 | CCACATGTGGACAGC[A/C]AGTAGACATTTGGGA | 25879 |
rs769362347 | snp | G/T | 3.45292e-05 | 0.00415493 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415112 | ACTCTAGTACTGAGG[G/T]GGCAAGAACGGGGCA | 25879 |
rs769399400 | snp | C/T | 1.6983e-05 | 0.00291397 | splice-donor-variant | DCAF13 | GRCh38.p7 | 8:103426147 | CAATATTAGGAAAGG[C/T]ACAAAAGTAAATTGA | 25879 |
rs769407655 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424906 | AGTTGTTAATAAGAT[A/G]TAGCCCTATTAAATA | 25879 |
rs769458251 | in-del | -/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414679 | AACGCGGACAGCAAC[-/G]GCTCCCTTCAACGCT | 25879 |
rs769461152 | in-del | -/ATGAA | 1.65048e-05 | 0.00287265 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103440219 | TTATGTGTGGATCTG[-/ATGAA]ATGAACATTCGCCTG | 25879 |
rs769462302 | snp | A/G | 1.65463e-05 | 0.00287626 | missense | DCAF13 | GRCh38.p7 | 8:103426063 | ATTTCTAGGTTGGTG[A/G]TGACAAAACTGTGAA | 25879 |
rs769564574 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413362 | AACCATTGTATAACA[A/G]GTACTTATAGAGGTA | 25879 |
rs769587274 | snp | A/G/T | 6.65196e-05 | 0.0057668 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415372 | GGAAAAGCGGAAGTC[A/G/T]CCTGTGGGAGGAGGT | 25879 |
rs769677268 | snp | A/G | 1.70035e-05 | 0.00291572 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414771 | GCAGCCCGGTGTCTG[A/G]GCGGGCTCTTACCGG | 25879 |
rs769718872 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103436467 | GTCTCGTGTGTGTCT[C/T]ATTTTGTAAGCACAT | 25879 |
rs769858416 | snp | A/G | 3.3923e-05 | 0.0041183 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415169 | GCGCGATGGAGGGGA[A/G]GTCCCAGCCTCTCCC | 25879 |
rs769906575 | snp | C/T | 3.57334e-05 | 0.00422675 | missense | DCAF13 | GRCh38.p7 | 8:103435637 | ACAGCTTATATACTT[C/T]TGATATGCGTGCACT | 25879 |
rs769990620 | in-del | -/AAG | 1.71522e-05 | 0.00292845 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432612 | TAAATCAGTGGGGAA[-/AAG]AAAAGGAAAGGAAGT | 25879 |
rs769994380 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442624 | TAAGAAGCAATTAAA[C/T]AAGTAAAGTTGATTT | 25879 |
rs770081762 | snp | C/T | 3.30278e-05 | 0.0040636 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441659 | TTACCCTTTTCTGAC[C/T]TCTGCTCTCATCTCA | 25879 |
rs770086436 | in-del | -/CTAG | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414271 | AATAGTATTTCGATT[-/CTAG]CTATTTTTTCACAGA | 25879 |
rs770090905 | snp | A/C/T | 3.36764e-05 | 0.00410333 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415205 | TCCGCCCTGCCTCGC[A/C/T]CACAAATGCTCCAGC | 25879 |
rs770091405 | snp | C/G | 4.94336e-05 | 0.00497135 | missense | DCAF13 | GRCh38.p7 | 8:103421010 | TCAGCGGAATTGTAT[C/G]CGTACAATACAAGCA | 25879 |
rs770179674 | snp | G/T | 3.66488e-05 | 0.00428055 | missense | DCAF13 | GRCh38.p7 | 8:103442827 | AACACAGCAAGCCTG[G/T]ATCTGTGCCACTTGT | 25879 |
rs770179934 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426442 | GAGAAAAAGATAGAA[G/T]TTCAGAAAATGCTTC | 25879 |
rs770203330 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435359 | CAAGGTAATTTTTGT[A/G]CTCTACTTTTTTTGA | 25879 |
rs770268158 | snp | A/T | 1.68957e-05 | 0.00290647 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415473 | GATGCTGAGCCGGAA[A/T]CCGGACAATTATGTC | 25879 |
rs770508219 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | DCAF13 | GRCh38.p7 | 8:103441552 | TAGCTCGTCATCGAC[A/G]TCTACCAAAATCTAT | 25879 |
rs770598143 | snp | A/G | 1.78321e-05 | 0.00298593 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426166 | AAAGTAAATTGACTA[A/G]TAGCTTGCCTATTAA | 25879 |
rs770598247 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425010 | ATCTTAGTACCAAAA[C/T]CTTTCCTGATCACTT | 25879 |
rs770687702 | snp | G/T | 1.69631e-05 | 0.00291226 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414778 | GGTGTCTGGGCGGGC[G/T]CTTACCGGCGAAGCG | 25879 |
rs770863424 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440397 | ATAGCTGTGATAAAA[-/A]AAAGCAATAAATGGA | 25879 |
rs770879623 | snp | C/T | 1.65061e-05 | 0.00287277 | missense | DCAF13 | GRCh38.p7 | 8:103435772 | TTCGAATCTTTCCTG[C/T]AGACAAAAGTCGAAG | 25879 |
rs770893372 | in-del | -/G | 1.65326e-05 | 0.00287507 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430595 | TTTGAACTGGTGATT[-/G]TTATACTTGTTTTTA | 25879 |
rs770940521 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422547 | TCAGTTTTGTGAACT[A/G]CTACAAAGAATAATG | 25879 |
rs770970108 | snp | A/G | 1.67691e-05 | 0.00289556 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420938 | GAACATTTTACATTT[A/G]TAGTTCACTGAAATT | 25879 |
rs771023999 | snp | A/G | 2.83821e-05 | 0.00376699 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442749 | GAAAGTTTTCTTTAA[A/G]ATGAGTTCCCATAAC | 25879 |
rs771058066 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | DCAF13 | GRCh38.p7 | 8:103421015 | GGAATTGTATCCGTA[C/T]AATACAAGCACATGA | 25879 |
rs771107739 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434992 | AAGCTTAACAATGCT[A/G]CTTGTAGGAATCTGT | 25879 |
rs771145987 | snp | G/T | 1.68139e-05 | 0.00289943 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415212 | TGCCTCGCCCACAAA[G/T]GCTCCAGCCCACGGA | 25879 |
rs771226415 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427863 | GAGGCTGTCCTGAAG[A/G]CTAAGCTAGCCCTTG | 25879 |
rs771232038 | snp | A/G | 1.67321e-05 | 0.00289236 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415254 | CTGCACAGCTAAAGA[A/G]CCGCCCCTTGCTAAC | 25879 |
rs771289592 | snp | G/T | 1.64868e-05 | 0.00287109 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103430656 | CAGGAATATAGTACT[G/T]TACGATATGAGGCAA | 25879 |
rs771316264 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429374 | TGTTATTTGAATTGC[A/G]TACAGACAGTAGGAG | 25879 |
rs771331385 | snp | A/T | 3.39219e-05 | 0.00411823 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415478 | TGAGCCGGAATCCGG[A/T]CAATTATGTCCGCGA | 25879 |
rs771664298 | snp | A/G | 3.50085e-05 | 0.00418366 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414963 | CCCGTCGACACCACG[A/G]CGCCCAGGGCCGCGG | 25879 |
rs771707465 | snp | C/G | 1.8887e-05 | 0.00307297 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414877 | GGTTCTCATACCGGA[C/G]GTGGCGGAATACCGT | 25879 |
rs771732933 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415757 | GGGAAACAGTTGTCT[A/C]TAGTGGAGAAAAATT | 25879 |
rs771798570 | snp | C/T | 1.65173e-05 | 0.00287374 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435794 | AAGTCGAAGCAGGTA[C/T]GTGCCTACCAGTAAG | 25879 |
rs771804248 | snp | G/T | 1.67722e-05 | 0.00289583 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415461 | GATGAAGGTGAAGAT[G/T]CTGAGCCGGAATCCG | 25879 |
rs771824732 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416493 | TTGCAAATCTCAGTG[A/C]GTTTCAGTCATCTTT | 25879 |
rs771885058 | snp | A/C/G | 3.35938e-05 | 0.00409829 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415218 | GCCCACAAATGCTCC[A/C/G]GCCCACGGACGCGGA | 25879 |
rs771978275 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422744 | ATCAGTCAAATAGAT[A/C]TTCCTTATTCTTTAT | 25879 |
rs772004021 | in-del | -/C | 4.95054e-05 | 0.00497496 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441647 | CATTTGACTCTATTA[-/C]CCTTTTCTGACTTCT | 25879 |
rs772114536 | snp | A/G | 0.000100336 | 0.00708223 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415257 | CACAGCTAAAGAACC[A/G]CCCCTTGCTAACGTT | 25879 |
rs772340116 | snp | C/T | 3.33378e-05 | 0.00408262 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420258 | GAAGGATCATTCTTA[C/T]TTCAGTTCCAAGAAA | 25879 |
rs772398473 | snp | A/C | 1.66629e-05 | 0.00288638 | missense | DCAF13 | GRCh38.p7 | 8:103432696 | ATACAATCTGTTGGA[A/C]CCCTATGGAAGCTTT | 25879 |
rs772511448 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438911 | TTAATGCCTTTCTTA[A/G]CACTTACTAATATAG | 25879 |
rs772515437 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439742 | AAAAAAAGTGTGTTG[-/A]CCTGAATTGATTTGA | 25879 |
rs772637995 | snp | A/C | 1.65411e-05 | 0.00287581 | missense | DCAF13 | GRCh38.p7 | 8:103426069 | AGGTTGGTGATGACA[A/C]AACTGTGAAGCAGTG | 25879 |
rs772725147 | snp | A/G | 0.000353878 | 0.0132971 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421245 | ACTAGTTTTCTTTAT[A/G]TAATTCAGCCTTCCC | 25879 |
rs772751571 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435143 | AAATTATTTGAACTT[A/C]TATATACAGCCATTA | 25879 |
rs772820363 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435472 | AAACTGTTGAAATTT[G/T]TCCTTATCCCTCACC | 25879 |
rs772923501 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423783 | GTACATCATAAATAT[A/T]TATCTTTTATTTGTA | 25879 |
rs773008806 | snp | A/G | 5.09359e-05 | 0.00504632 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414775 | CCCGGTGTCTGGGCG[A/G]GCTCTTACCGGCGAA | 25879 |
rs773022259 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414524 | AATCAGGCTTTGAAT[A/C]CCATCTTCTCTGCCA | 25879 |
rs773038401 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440353 | GAAAATTTACTTTTA[A/G]GTATTTTTGGGTATT | 25879 |
rs773044414 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432550 | TCTCTTCCCATTGCA[C/T]TGAGCTGAGTACTTT | 25879 |
rs773132846 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431520 | TGAAGTAGATAAATA[C/T]GATAATCTTTCCAAA | 25879 |
rs773208949 | in-del | -/TAT | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416272 | TGGTTGAGTAGGAGA[-/TAT]TATCAACATGTGTGT | 25879 |
rs773291851 | snp | A/T | 1.69203e-05 | 0.00290859 | stop-gained | DCAF13 | GRCh38.p7 | 8:103420408 | ATGGAGTCAATTGCT[A/T]GGCAAAGCATCCAGA | 25879 |
rs773293726 | snp | C/G | 3.56449e-05 | 0.00422151 | missense | DCAF13 | GRCh38.p7 | 8:103435639 | AGCTTATATACTTTT[C/G]ATATGCGTGCACTGG | 25879 |
rs773303896 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419462 | AAGTAAGTAAACAAA[C/T]ATAGAAAGTGCTCAG | 25879 |
rs773354710 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434209 | AAGTTCAAGTCTAGG[A/C]CGACCAGTAATTACT | 25879 |
rs773389061 | snp | C/T | 0.000119526 | 0.00772974 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415171 | GCGATGGAGGGGAGG[C/T]CCCAGCCTCTCCCGA | 25879 |
rs773394170 | snp | A/G | | | missense | DCAF13 | GRCh38.p7 | 8:103420276 | CAGTTCCAAGAAACT[A/G]TGATCCTGCTTTACA | 25879 |
rs773396420 | snp | A/T | 6.60131e-05 | 0.00574476 | missense | DCAF13 | GRCh38.p7 | 8:103427164 | GTGGACAGCAAGTAG[A/T]CATTTGGGATGAACA | 25879 |
rs773486449 | snp | G/T | 1.66493e-05 | 0.0028852 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415419 | CCTAGCGGACACCTC[G/T]TGGAGTCCGGCCGGA | 25879 |
rs773540553 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426481 | TAGTTGATGTCATCA[C/T]AGATCTTACACAAAA | 25879 |
rs773752617 | snp | C/T | 1.68997e-05 | 0.00290682 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415474 | ATGCTGAGCCGGAAT[C/T]CGGACAATTATGTCC | 25879 |
rs773776764 | snp | C/T | 1.66297e-05 | 0.0028835 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415374 | AAAAGCGGAAGTCGC[C/T]TGTGGGAGGAGGTGG | 25879 |
rs773781395 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416705 | TGGTTAATAGTCTTT[C/T]CCATCAGACTTAGCC | 25879 |
rs773797811 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424664 | TCATTTACAAGCAAA[C/T]TCAGTCTTGAGCTTG | 25879 |
rs773839769 | snp | A/G | 6.86412e-05 | 0.00585798 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414911 | CCACGCCGACGACCC[A/G]GACGCCGACTGGCCC | 25879 |
rs773865091 | snp | A/G | 1.66955e-05 | 0.0028892 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415334 | GCCGCCGCTCCGCGA[A/G]TCACGTGACTGGAAG | 25879 |
rs773968470 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425070 | CTGTTTTGCAAGAAG[C/T]GTTTTCCTTTTTGAA | 25879 |
rs774063632 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414705 | ACGCTCCTCCTCCCC[C/G]TAGAACGGAAAAGAC | 25879 |
rs774081250 | snp | C/T | 1.65094e-05 | 0.00287305 | stop-gained | DCAF13 | GRCh38.p7 | 8:103435783 | CCTGTAGACAAAAGT[C/T]GAAGCAGGTATGTGC | 25879 |
rs774086841 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428425 | TGGCAGAGTTAAGTA[A/T]TTGCCACAGAGACCA | 25879 |
rs774132040 | snp | A/T | 3.59725e-05 | 0.00424087 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414859 | CGCTCACGCCCGCTA[A/T]CAGGTTCTCATACCG | 25879 |
rs774146109 | snp | C/G | 1.72139e-05 | 0.00293371 | missense | DCAF13 | GRCh38.p7 | 8:103435660 | CGTGCACTGGACACT[C/G]CTGTAATGGTCCATA | 25879 |
rs774171051 | snp | A/G | 6.59033e-05 | 0.00573997 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421016 | GAATTGTATCCGTAC[A/G]ATACAAGCACATGAA | 25879 |
rs774181241 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414376 | ATTCGCTGAAGATTA[C/T]GCCCTATCCCAATAC | 25879 |
rs774270409 | snp | A/C/T | 4.95244e-05 | 0.00497596 | synonymous-codon, stop-gained | DCAF13 | GRCh38.p7 | 8:103420347 | GCTACCAAACTGGAA[A/C/T]GAGTATTTGCAAAAC | 25879 |
rs774282121 | in-del | -/A | 1.69513e-05 | 0.00291125 | utr-variant-5-prime, splice-donor-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414781 | TCTGGGCGGGCTCTT[-/A]ACCGGCGAAGCGGAT | 25879 |
rs774415757 | snp | C/T | 1.69284e-05 | 0.00290928 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415178 | AGGGGAGGTCCCAGC[C/T]TCTCCCGAGTCTCCG | 25879 |
rs774479851 | snp | G/T | 1.65059e-05 | 0.00287275 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103427186 | GGATGAACAAAGAAC[G/T]AATCCTATATGTTCA | 25879 |
rs774528771 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434875 | TCACCCTTTGAAAGG[A/C]CATGTTCACTCTTAC | 25879 |
rs774534670 | snp | C/T | 1.68119e-05 | 0.00289926 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415214 | CCTCGCCCACAAATG[C/T]TCCAGCCCACGGACG | 25879 |
rs774548497 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429561 | CTGGATGATAGAGGG[C/T]TTATTTTTACTTAAT | 25879 |
rs774558109 | snp | A/T | 1.91826e-05 | 0.00309693 | missense | DCAF13 | GRCh38.p7 | 8:103442851 | CACTTGTGTCAGAGA[A/T]GAAGAAACACGTAGT | 25879 |
rs774567655 | snp | C/T | 3.56729e-05 | 0.00422317 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427321 | CTGTTTAGAAAACTT[C/T]TGAATGTATGATAGA | 25879 |
rs774655943 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428105 | CCTGATAAAAGATAG[A/G]AAGTAAGGTTGAGTC | 25879 |
rs774743747 | snp | G/T | 1.68332e-05 | 0.00290109 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420247 | TGAATTATTAAGAAG[G/T]ATCATTCTTATTTCA | 25879 |
rs774804836 | in-del | -/ATT | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425472 | TATGTCTTTACTAAC[-/ATT]ATGAAAATAGTTTTG | 25879 |
rs774888842 | snp | A/G | | | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414717 | CCCCTAGAACGGAAA[A/G]GACGGAGGAGATCCA | 25879 |
rs774906526 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422552 | TTTGTGAACTACTAC[A/G]AAGAATAATGAAAAA | 25879 |
rs774918328 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416625 | CCCGCCCCCTTCAGC[A/G]CCCGTCTTCTGTGAT | 25879 |
rs774923967 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | DCAF13 | GRCh38.p7 | 8:103440226 | TGGATCTGATGAAAT[A/G]AACATTCGCCTGTGG | 25879 |
rs775026329 | snp | C/G | 1.68972e-05 | 0.0029066 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414794 | CTTACCGGCGAAGCG[C/G]ATCTTCACGAGGTCG | 25879 |
rs775039881 | snp | A/G | 1.69352e-05 | 0.00290987 | missense | DCAF13 | GRCh38.p7 | 8:103435675 | CCTGTAATGGTCCAT[A/G]TGGATCATGTATCTG | 25879 |
rs775053940 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439991 | CTTATTAGTTGGGTT[C/T]AATAAAAATACATTG | 25879 |
rs775129996 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435822 | AAGCCATTTATATTC[A/G]TATGTCACTTAACAA | 25879 |
rs775190762 | snp | A/G | 2.02965e-05 | 0.00318557 | utr-variant-5-prime, missense, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414891 | ACGTGGCGGAATACC[A/G]TGCTCCACGCCGACG | 25879 |
rs775237892 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421556 | AACTTTTTCATCATC[C/T]CCAGCTGAAACTATA | 25879 |
rs775306856 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421025 | CCGTACAATACAAGC[A/G]CATGAAGGCTTTGTA | 25879 |
rs775308251 | snp | A/G | 0.000150114 | 0.00866224 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421110 | CCATTAAGTCATTAA[A/G]TTTGATCAACATAGG | 25879 |
rs775326465 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422758 | TCTTCCTTATTCTTT[A/G]TTTACTGGTGACTTT | 25879 |
rs775411262 | snp | C/G/T | 0.000198633 | 0.00996407 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427339 | AATGTATGATAGAAA[C/G/T]TTCTGAATTTTAATG | 25879 |
rs775707351 | snp | A/G | 1.64931e-05 | 0.00287163 | missense | DCAF13 | GRCh38.p7 | 8:103430675 | GATATGAGGCAAGCT[A/G]CTCCTTTGAAAAAGG | 25879 |
rs775709052 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429888 | ATATCAAAAGCCATA[A/G]AATTGTTCATACCTT | 25879 |
rs775787723 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435367 | TTTTTGTACTCTACT[C/T]TTTTTGAAATTTCCA | 25879 |
rs775796517 | snp | A/G | 1.66796e-05 | 0.00288782 | missense | DCAF13 | GRCh38.p7 | 8:103420384 | TTGCTTCGCTGGATG[A/G]TCACCGTGATGGAGT | 25879 |
rs775796602 | snp | A/G | 3.60198e-05 | 0.00424366 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415070 | CGAGAGGACTCTTAT[A/G]CCCAAGGCGCGTGAG | 25879 |
rs775798982 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417893 | GGGAGGCCGAGGCGG[A/G]AAGATCACGAGGTCA | 25879 |
rs775869728 | in-del | -/AAAGG | 1.71334e-05 | 0.00292684 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432616 | TCAGTGGGGAAAAGA[-/AAAGG]AAAGGAAGTGGGAAA | 25879 |
rs775871799 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431108 | AACTCATTCACGTAA[A/C]CAGCTTTATTTGTTC | 25879 |
rs775938599 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422833 | CAGGTTGGCTGGGTG[C/T]AGAAGCTAGATTGCA | 25879 |
rs776069612 | in-del | -/GAAAA | 0.000137379 | 0.00828678 | intron-variant | DCAF13 | GRCh38.p7 | 8:103432609 | GCTTAAATCAGTGGG[-/GAAAA]GAAAAGGAAAGGAAG | 25879 |
rs776075764 | snp | A/G | 1.65051e-05 | 0.00287267 | missense | DCAF13 | GRCh38.p7 | 8:103440201 | CTTCTGACAGCAAGT[A/G]TATTATGTGTGGATC | 25879 |
rs776083140 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434482 | ACTGTTCTTAGGCAG[A/G]AACTGTAAAGCAGTT | 25879 |
rs776153682 | snp | G/T | 3.30693e-05 | 0.00406615 | missense | DCAF13 | GRCh38.p7 | 8:103426083 | AAAACTGTGAAGCAG[G/T]GGAAAATGGATGGGC | 25879 |
rs776163991 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424089 | AGTGGCATGATCTCT[A/G]CTCACTGCAAGCTCT | 25879 |
rs776182266 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438924 | TAACACTTACTAATA[C/T]AGTATCACCTGTGAA | 25879 |
rs776192350 | snp | C/G | 1.64773e-05 | 0.00287026 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421034 | ACAAGCACATGAAGG[C/G]TTTGTACGAGGAATA | 25879 |
rs776213749 | snp | C/T | 3.85676e-05 | 0.00439116 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414987 | GCCGCGGAGGTGGGA[C/T]GCGATGCAGTGGCCG | 25879 |
rs776276050 | snp | A/T | 1.68187e-05 | 0.00289984 | intron-variant | DCAF13 | GRCh38.p7 | 8:103421123 | AAATTTGATCAACAT[A/T]GGTAAGAATAATCTA | 25879 |
rs776338512 | in-del | -/TTAG | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439849 | TTGCATTTTATGCTT[-/TTAG]TTATTCTGTGAACTT | 25879 |
rs776368561 | snp | C/T | 1.67136e-05 | 0.00289076 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415269 | ACCGCCCCTTGCTAA[C/T]GTTTGCCGGCAAAAC | 25879 |
rs776458672 | snp | A/G | 1.67489e-05 | 0.00289381 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415318 | CCAGTTGAGCCAGCA[A/G]GCCGCCGCTCCGCGA | 25879 |
rs776464829 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413247 | CAATGATCACCTCGA[C/G]TATCACCTCTTCTGC | 25879 |
rs776528395 | snp | A/G | 1.64939e-05 | 0.0028717 | missense | DCAF13 | GRCh38.p7 | 8:103420302 | TTACATCCTTTTGAG[A/G]TCCCACGAGAATATA | 25879 |
rs776685812 | in-del | -/A | 3.58301e-05 | 0.00423247 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415074 | AGGACTCTTATGCCC[-/A]AGGCGCGTGAGCGAA | 25879 |
rs776723629 | in-del | -/TT | 0.000115776 | 0.00760754 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430708 | AGTTTCAGTTTTGAC[-/TT]TTGCTTTATACAGTT | 25879 |
rs776792298 | snp | A/G | 1.69648e-05 | 0.00291241 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415164 | GGAAAGCGCGATGGA[A/G]GGGAGGTCCCAGCCT | 25879 |
rs776808717 | snp | C/T | 1.66551e-05 | 0.00288571 | missense | DCAF13 | GRCh38.p7 | 8:103432711 | ACCCTATGGAAGCTT[C/T]CATTTTTACAGCAGC | 25879 |
rs776825554 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103431234 | GACTTACATATCAGA[A/G]CTAATAATACAACTT | 25879 |
rs776835867 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434412 | TTCCCATGTAGAAAT[A/G]AAGCATCTTACTAAA | 25879 |
rs776835973 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | DCAF13 | GRCh38.p7 | 8:103441569 | CTACCAAAATCTATC[C/T]ATAGCCAGATTCAGG | 25879 |
rs776915582 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419293 | TGGCTCCACCGTGTC[A/G]TATTCGAGTTACTTA | 25879 |
rs776931410 | snp | A/G | 0.000109655 | 0.00740375 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426181 | ATAGCTTGCCTATTA[A/G]CATTCTTTTATTTAA | 25879 |
rs776931538 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103425431 | TTTACTATTTGTGCA[G/T]CTGTCAGCACAGTGA | 25879 |
rs776944880 | snp | A/G | 1.65416e-05 | 0.00287586 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441466 | TCAGCTTACATCACG[A/G]GAAAAAGCAGCCAAG | 25879 |
rs776995991 | snp | A/G | | | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414806 | GCGGATCTTCACGAG[A/G]TCGAGCGGATGCAGC | 25879 |
rs777001784 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420134 | ACAGGTCTTCTACTT[C/T]TGTATTCTTAGTGTT | 25879 |
rs777116764 | snp | A/G | 1.6501e-05 | 0.00287232 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441643 | GAGGCATTTGACTCT[A/G]TTACCCTTTTCTGAC | 25879 |
rs777198875 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420478 | GGCAAGTGTCAATCT[A/G]GATGATATTTTCAAC | 25879 |
rs777212643 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426422 | TTTCCCATGGGAAGA[A/C]CACGGAGAAAAAGAT | 25879 |
rs777219397 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419902 | TAATCCCAGCTACTC[A/G]GGTGGCTGAGGCAGG | 25879 |
rs777291787 | snp | A/G | 1.66288e-05 | 0.00288343 | stop-gained, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415388 | CCTGTGGGAGGAGGT[A/G]GCGGTGGGCGGAACT | 25879 |
rs777313940 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434128 | TTGTATCCCTTTTCT[A/G]TATTTGTAAGTATTT | 25879 |
rs777363133 | snp | A/G | 1.65405e-05 | 0.00287576 | missense | DCAF13 | GRCh38.p7 | 8:103427106 | TTAAAGACAGTGTAT[A/G]CTGGGATTGATCATC | 25879 |
rs777369507 | snp | A/C | 1.6951e-05 | 0.00291122 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415142 | ACAGACACTACGTCA[A/C]GCCGGCGGAAAGCGC | 25879 |
rs777408138 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103442295 | TATTTTCCAAGTTAA[A/G]GAATTAATCTATAGT | 25879 |
rs777442182 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435916 | TGCACTTAAACAAAA[C/T]TAGATGGTATAACGT | 25879 |
rs777448462 | snp | A/G | 1.66421e-05 | 0.00288458 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415412 | CGGAACTCCTAGCGG[A/G]CACCTCGTGGAGTCC | 25879 |
rs777465353 | snp | C/T | 0.000164739 | 0.00907428 | missense | DCAF13 | GRCh38.p7 | 8:103441542 | ATAAAACGTATAGCT[C/T]GTCATCGACATCTAC | 25879 |
rs777471920 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103435948 | TTGCACACCTAGGCT[A/G]TGTGGTCATATGATA | 25879 |
rs777488699 | in-del | -/A | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414678 | CCAACGCGGACAGCA[-/A]CGCTCCCTTCAACGC | 25879 |
rs777555380 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441622 | TCGTCGACGAAAGTA[C/T]GTTTTGAGGCATTTG | 25879 |
rs777574955 | in-del | -/AAG | 0.000878149 | 0.0209357 | intron-variant | DCAF13 | GRCh38.p7 | 8:103442747 | GAGAAAGTTTTCTTT[-/AAG]ATGAGTTCCCATAAC | 25879 |
rs777582771 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420793 | TAGAATCAACAGAGT[A/G]TTTGTCAGGTTGTAT | 25879 |
rs777686799 | snp | A/G | 3.40038e-05 | 0.00412319 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414827 | CGGATGCAGCGCAAG[A/G]TTGGATAAGACGCCG | 25879 |
rs777709512 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103419113 | ATGGTCTCGATCTCC[C/T]GACCTCGTGATCCGT | 25879 |
rs777762066 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103426966 | CCCCTTTAAGTAAGG[A/G]CTTCAAAGAAGTTTC | 25879 |
rs777763426 | snp | G/T | 1.66885e-05 | 0.00288859 | stop-gained, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415444 | GCCGGAAGAGCAACC[G/T]AGATGAAGGTGAAGA | 25879 |
rs777774840 | snp | C/T | 6.16903e-05 | 0.0055535 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414943 | GGCCCGTCATAGGCT[C/T]GGGGCCCGTCGACAC | 25879 |
rs777815512 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434942 | TTGGCAGTGATTTGG[C/T]AACTCAAATCAAGCC | 25879 |
rs777843588 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421148 | AATCTAATTGAATAC[-/A]TTTTTTTTCAAGTTC | 25879 |
rs777857340 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432604 | TATTTGCTTAAATCA[A/G]TGGGGAAAAGAAAAG | 25879 |
rs778048080 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103427379 | CATTTTGTCAGTTTT[A/C]CCGATTGTAAATGAG | 25879 |
rs778048907 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | DCAF13 | GRCh38.p7 | 8:103421011 | CAGCGGAATTGTATC[C/T]GTACAATACAAGCAC | 25879 |
rs778134995 | snp | C/G | 1.64822e-05 | 0.00287068 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103421058 | AGGAATATGTACTCG[C/G]TTTTGTGGGACTTCT | 25879 |
rs778152770 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423139 | TTGATTGGCAAGTGG[A/G]AATGGATGGCACCTA | 25879 |
rs778266113 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429287 | GGAAGTCTCAGAAAA[A/G]CAGCCATTAAGATAG | 25879 |
rs778281499 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440901 | AGAAGGAAAGGGTAA[A/G]TGTGAATTATTTTCT | 25879 |
rs778323175 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103412917 | AAATTATAGTATGTT[A/G]CTCAGCACTGATGTT | 25879 |
rs778339663 | snp | C/T | 1.68761e-05 | 0.00290478 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415195 | CTCCCGAGTCTCCGC[C/T]CTGCCTCGCCCACAA | 25879 |
rs778482042 | in-del | -/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433138 | ATGTTTAACATTTGG[-/C]CCTTTACAGAAGAAG | 25879 |
rs778509989 | snp | C/T | 0.00025104 | 0.0112008 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415454 | CAACCGAGATGAAGG[C/T]GAAGATGCTGAGCCG | 25879 |
rs778515435 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441638 | GTTTTGAGGCATTTG[A/G]CTCTATTACCCTTTT | 25879 |
rs778559287 | in-del | -/AAAACA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418533 | ATGATACCGCATCTC[-/AAAACA]AAAACAAAAACAAAA | 25879 |
rs778595960 | snp | A/C | 3.2188e-05 | 0.0040116 | utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414950 | CATAGGCTCGGGGCC[A/C]GTCGACACCACGGCG | 25879 |
rs778609059 | snp | C/G | 1.65048e-05 | 0.00287265 | missense | DCAF13 | GRCh38.p7 | 8:103427154 | TTTGCCACATGTGGA[C/G]AGCAAGTAGACATTT | 25879 |
rs778698939 | snp | A/G | 3.38472e-05 | 0.00411369 | missense | DCAF13 | GRCh38.p7 | 8:103427247 | GTTAAATTTAACCCA[A/G]TTGAGGTAATGTTTT | 25879 |
rs778728272 | in-del | -/A | 3.29766e-05 | 0.00406045 | | | GRCh38.p7 | 8:103441492 | CCAAGGATTATAACC[-/A]GAAATTGAAGGAGAA | 25879 |
rs778805235 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103416401 | GGCATCGTTCCCAGT[C/T]CTTGAATCTCTGGTC | 25879 |
rs778820655 | snp | A/C/G | 4.12331e-05 | 0.00454039 | intron-variant | DCAF13 | GRCh38.p7 | 8:103440316 | TAAAGCTGATTTCTA[A/C/G]TTTTATTAGATATTA | 25879 |
rs778860828 | in-del | -/AAAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418139 | TCTCAAAAAAAAAAG[-/AAAA]AAAAAGACATCTGAT | 25879 |
rs778880688 | snp | A/G | 4.60904e-05 | 0.00480032 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415033 | TCGCCCCTTGTGAGC[A/G]CAACCCCACCTCCGG | 25879 |
rs778923641 | snp | A/G | 1.70828e-05 | 0.00292252 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103440142 | TTTCTATAGGGAGGT[A/G]TATCATACAAAGAGA | 25879 |
rs778941810 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103434065 | CATATCCCTTATAAT[A/G]AGTGACTGTTGGAGT | 25879 |
rs779011580 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422565 | ACAAAGAATAATGAA[A/G]AATGAAGACTGAGGA | 25879 |
rs779148453 | in-del | -/ATTAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439293 | ACCGCACCTGGCTCT[-/ATTAA]ATTATTCTTACCTCA | 25879 |
rs779187468 | snp | C/G | 3.34526e-05 | 0.00408965 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415255 | TGCACAGCTAAAGAA[C/G]CGCCCCTTGCTAACG | 25879 |
rs779207287 | snp | C/T | 8.24382e-05 | 0.00641968 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103430659 | GAATATAGTACTGTA[C/T]GATATGAGGCAAGCT | 25879 |
rs779277663 | snp | C/G | 1.67365e-05 | 0.00289275 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415309 | GCGCAGGATCCAGTT[C/G]AGCCAGCAGGCCGCC | 25879 |
rs779290931 | snp | A/G | 1.66676e-05 | 0.00288679 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103432685 | TATGAGAACAAATAC[A/G]ATCTGTTGGAACCCT | 25879 |
rs779292049 | snp | A/G | | | splice-donor-variant | DCAF13 | GRCh38.p7 | 8:103427253 | TTTAACCCAATTGAG[A/G]TAATGTTTTTTTTTA | 25879 |
rs779395446 | snp | A/T | 1.83471e-05 | 0.00302873 | intron-variant | DCAF13 | GRCh38.p7 | 8:103427264 | TGAGGTAATGTTTTT[A/T]TTTAAGTATGTTTTA | 25879 |
rs779408163 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439686 | AGGAGGTACTCTTTG[A/G]AGACCATTGCATTTC | 25879 |
rs779417607 | in-del | -/AT | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424443 | ACAGTGTTGCAAAAC[-/AT]AAACTTTTATTACCT | 25879 |
rs779454169 | snp | C/G | 6.85624e-05 | 0.00585461 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414737 | GAGGAGATCCAGTTC[C/G]GGCTGACAGTGAGAG | 25879 |
rs779521388 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441198 | AACTCAGTGATCCAC[A/G]TGGCCCTACTCCTTC | 25879 |
rs779581442 | snp | A/T | 3.55853e-05 | 0.00421798 | utr-variant-3-prime | DCAF13 | GRCh38.p7 | 8:103442914 | TCCTGATGTATAATT[A/T]TTTGTTACTTTTGAT | 25879 |
rs779588455 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415556 | GGGACGGTTTCCGCA[A/T]GTCGTTGGGTCTAGC | 25879 |
rs779659837 | snp | A/T | 1.65176e-05 | 0.00287376 | intron-variant | DCAF13 | GRCh38.p7 | 8:103430603 | GGTGATTGTTATACT[A/T]GTTTTTAGACATTTC | 25879 |
rs779664874 | in-del | -/AT | 3.33572e-05 | 0.00408381 | frameshift-variant | DCAF13 | GRCh38.p7 | 8:103440262 | TAATGCTTCTGAAAA[-/AT]TGGGTGTGGTAAGAG | 25879 |
rs779711660 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441379 | TAGGTTAGGGGGAAA[A/G]GGGTGCTTTCTAGCT | 25879 |
rs779761648 | snp | A/C | 1.68448e-05 | 0.00290209 | synonymous-codon, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415468 | GTGAAGATGCTGAGC[A/C]GGAATCCGGACAATT | 25879 |
rs779779163 | snp | A/T | 1.65784e-05 | 0.00287905 | missense | DCAF13 | GRCh38.p7 | 8:103440170 | AGAATGCAACATGTT[A/T]TCTGTGTAAAATGGA | 25879 |
rs779845334 | snp | G/T | 2.01802e-05 | 0.00317643 | intron-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415557 | GGACGGTTTCCGCAA[G/T]TCGTTGGGTCTAGCC | 25879 |
rs779876487 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424775 | TAAGTGCTAAAATGT[C/T]TCTTTGGGTCAAGCC | 25879 |
rs779935311 | snp | C/G | 2.11044e-05 | 0.00324835 | missense, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415039 | CTTGTGAGCGCAACC[C/G]CACCTCCGGGACCAA | 25879 |
rs779950308 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438998 | TTGACATCTCCATTT[A/G]TTAAATGATTCTTTT | 25879 |
rs779984350 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433976 | TTTTAGCAAGGTACC[A/G]TTTTTCAGAGTGTCC | 25879 |
rs780018049 | snp | C/G | 0.000116464 | 0.00763009 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415352 | ACGTGACTGGAAGTA[C/G]TCTGGGAAAAGCGGA | 25879 |
rs780025421 | snp | C/T | 6.99631e-05 | 0.00591411 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415092 | GCGCGTGAGCGAAGC[C/T]GGAGACTCTAGTACT | 25879 |
rs780063759 | in-del | -/ATT | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103437690 | GGTTTGTTTCCTATC[-/ATT]ATAAACATCAAATAA | 25879 |
rs780155775 | snp | C/T | 1.66613e-05 | 0.00288623 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103432697 | TACAATCTGTTGGAA[C/T]CCTATGGAAGCTTTC | 25879 |
rs780324373 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423709 | TGTGAGGTAACAGAT[A/G]TGTTAATTAGCTTGG | 25879 |
rs780365237 | snp | A/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439324 | CTCAACTTATCAGAC[A/T]CTTCTGTAGTCCTCC | 25879 |
rs780424597 | snp | C/G | 1.64876e-05 | 0.00287116 | missense | DCAF13 | GRCh38.p7 | 8:103420990 | GTTAGAATTTGGAAT[C/G]TAACTCAGCGGAATT | 25879 |
rs780426647 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420778 | AGTTTTGTAACACTT[C/T]AGAATCAACAGAGTA | 25879 |
rs780450654 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421913 | GCTATTGTGAATAGT[A/G]TTGCCGTGACCATTG | 25879 |
rs780519424 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103420060 | ACCTAGGGTCTAATT[A/G]TTTTGCAAGATGTAT | 25879 |
rs780526815 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103417375 | GGCTGGGCGTGGTGG[C/T]TTATGCCTGTAATCC | 25879 |
rs780530499 | snp | A/C | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432349 | CCTAAGCTCACCATT[A/C]ATTTTGCCCCTAATT | 25879 |
rs780534388 | snp | A/G | 1.69507e-05 | 0.0029112 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415149 | CTACGTCACGCCGGC[A/G]GAAAGCGCGATGGAG | 25879 |
rs780640550 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430541 | GGGCAATTAAATCAT[C/T]TGTTTACTGAATGGA | 25879 |
rs780799202 | in-del | -/AAAAC | 0.00028302 | 0.0118924 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426039 | TACCATCATCATAAT[-/AAAAC]AAATATTTCTAGGTT | 25879 |
rs780807055 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | DCAF13 | GRCh38.p7 | 8:103441526 | TCAGCATTATCCTCA[C/T]ATAAAACGTATAGCT | 25879 |
rs780867938 | snp | C/G | 1.86618e-05 | 0.00305459 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415056 | ACCTCCGGGACCAAC[C/G]AGAGGACTCTTATGC | 25879 |
rs780886381 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103413738 | GATTTTCCTTCATAG[A/C]ACGGGTTCTTGCTTC | 25879 |
rs780905173 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103424829 | AGATTACATCTTAGT[C/T]TCCCAGTAGAATCAG | 25879 |
rs780907583 | snp | A/C | 1.73174e-05 | 0.00294251 | intron-variant | DCAF13 | GRCh38.p7 | 8:103441420 | GAAGCAAAACAACAC[A/C]CTATTCATTAAGATA | 25879 |
rs780922617 | snp | A/T | 0.00024899 | 0.0111549 | intron-variant | DCAF13 | GRCh38.p7 | 8:103426049 | ATAATAAAACAAATA[A/T]TTCTAGGTTGGTGAT | 25879 |
rs780937554 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433667 | TATGACTTTCTGCTA[A/G]AAAGAGGTTTAGTCC | 25879 |
rs780957947 | snp | A/G | 1.72809e-05 | 0.00293941 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415110 | AGACTCTAGTACTGA[A/G]GGGGCAAGAACGGGG | 25879 |
rs781010399 | snp | C/T | 1.66515e-05 | 0.00288539 | missense | DCAF13 | GRCh38.p7 | 8:103426126 | ACGAGGAAGAGCCAT[C/T]ACATACAATATTAGG | 25879 |
rs781102522 | snp | C/G | 3.32712e-05 | 0.00407854 | missense, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415363 | AGTAGTCTGGGAAAA[C/G]CGGAAGTCGCCTGTG | 25879 |
rs781110677 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414381 | CTGAAGATTACGCCC[C/T]ATCCCAATACTAGTC | 25879 |
rs781123809 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421569 | TCCCCAGCTGAAACT[A/G]TAGTCATTAAACAAT | 25879 |
rs781148394 | in-del | -/A | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429706 | CACGAAGAAACATTT[-/A]ACTAATAAAACAATA | 25879 |
rs781158650 | snp | C/G | 1.69413e-05 | 0.00291039 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414821 | GTCGAGCGGATGCAG[C/G]GCAAGGTTGGATAAG | 25879 |
rs781198907 | snp | A/C/G | 8.3563e-05 | 0.00646339 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415289 | GCCGGCAAAACTACG[A/C/G]AGCGGCGCAGGATCC | 25879 |
rs781255001 | snp | G/T | 0.000136147 | 0.00824954 | intron-variant | DCAF13 | GRCh38.p7 | 8:103420528 | AATGTTTTCCCTTTA[G/T]TTTTTAGTTACTGTA | 25879 |
rs781274066 | snp | C/T | 1.70139e-05 | 0.00291662 | utr-variant-5-prime, intron-variant | DCAF13, SLC25A32 | GRCh38.p7 | 8:103414769 | ATGCAGCCCGGTGTC[C/T]GGGCGGGCTCTTACC | 25879 |
rs781293279 | in-del | -/AG | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103421332 | GAGGTAAGTCTAGAA[-/AG]AGTTTGGCTTACTCT | 25879 |
rs781458367 | snp | A/G | 1.82577e-05 | 0.00302134 | intron-variant | DCAF13 | GRCh38.p7 | 8:103435622 | TTTAAAAATTCTTTT[A/G]CAGCTTATATACTTT | 25879 |
rs781519446 | snp | A/C | 1.67377e-05 | 0.00289284 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF13, SLC25A32 | GRCh38.p7 | 8:103415245 | CGGAAGCGACTGCAC[A/C]GCTAAAGAACCGCCC | 25879 |
rs781549097 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | DCAF13 | GRCh38.p7 | 8:103421000 | GGAATCTAACTCAGC[A/G]GAATTGTATCCGTAC | 25879 |
rs781677449 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103430800 | AATTAAAAAAATCTT[C/T]TATACAGGTGTTCTT | 25879 |
rs781689323 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103441998 | TCTCAATCTCCTGAC[C/T]TCGTGATCGCCTGCC | 25879 |
rs781722409 | snp | C/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103422138 | TTTGGAGGATTGACA[C/G]GTTTGACAACTGAGA | 25879 |
rs796220013 | snp | G/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429840 | ATTGTAGTGTATACT[G/T]GTACAGCTCTTTGGA | 25879 |
rs796431064 | in-del | -/AAAA | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103440397 | CATAGCTGTGATAAA[-/AAAA]GCAATAAATGGACAA | 25879 |
rs796489653 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103429116 | CCAAAAGTTTATGCT[A/G]ATCATTGGGACGTTT | 25879 |
rs796563451 | snp | C/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103438279 | AAAAGCAGTCTATCT[C/T]ATCTAGTTTTCATTT | 25879 |
rs796715704 | multinucleotide-polymorphism | AT/GC | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103433132 | TGAAAATGTTTAACA[AT/GC]TGGCCCTTTACAGAA | 25879 |
rs796748512 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103423221 | AGAGGACTTAGTGTA[-/T]TTTTTTTTTAATGCT | 25879 |
rs796799560 | in-del | -/TTTTTTTT | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103439384 | TCACTTTAATTAAGC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 25879 |
rs796912713 | in-del | -/T | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103428917 | AGCTGTTTTTTTTTT[-/T]AATTGCTATTAACCT | 25879 |
rs796932256 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103418118 | GGGCAACAGAGCAAG[A/G]CTCCGTCTCAAAAAA | 25879 |
rs796987460 | snp | A/G | | | intron-variant | DCAF13 | GRCh38.p7 | 8:103432622 | GGGAAAAGAAAAGGA[A/G]AGGAAGTGGGAAATT | 25879 |