SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs150126357 | snp | A/G | 0.000280077 | 0.0118305 | missense | DCAF5 | GRCh38.p7 | 14:69054761 | GCCCGGCTTGGTTGA[A/G]TCTCTAGCGTGGAAG | 8816 |
rs150158627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095251 | GTCTCTACTCCTTCA[C/G]AGAAGTGGCCACCAA | 8816 |
rs150167873 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144563 | GCCGGGGCGACAGAG[C/T]GAGACTCCGTTTAAA | 8816 |
rs150178608 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109299 | CAGTGAGTTGAGATC[A/G]CGCCACTCTAGCCTG | 8816 |
rs150179976 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118169 | CCCGAATGTCCCAAA[C/T]GAGAACCCGGCCATC | 8816 |
rs150221246 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153967 | GATAAATTTGCACGA[C/T]ACAAGAAGCGTGATT | 8816 |
rs150239157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075638 | AGGCACACGCCACCA[C/T]GCCCAGCTAATTTTT | 8816 |
rs150291468 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081468 | TTCTGTGGTCCAAGA[A/G]GGCAAGCTATTTACT | 8816 |
rs150315177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133279 | CTCCTTACCATGATG[C/G]AATCCAGCCTCGCAA | 8816 |
rs150333304 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100392 | AACTGACCCATAGGA[-/T]TCTGGTACAAATGCT | 8816 |
rs150368831 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140295 | GAGAGAGAGAGAAGA[C/T]AGAGAAAGACATTCT | 8816 |
rs150387419 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065229 | AGCCTCCTGAGTAGC[C/T]GGGATTACAGGCATC | 8816 |
rs150429483 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106767 | AAAGCTGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 8816 |
rs150451313 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121651 | GAACACAGGTAGATA[A/C/T]CCAGTGGGAAAATCT | 8816 |
rs150558404 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077336 | GCCTCCCCAGGAGAT[A/G]GAACACAGGCATGCA | 8816 |
rs150567803 | snp | A/G/T | 0.0058183 | 0.0536231 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054211 | GGCACAGATGGTTTC[A/G/T]AGGCTCCTCTCCTCA | 8816 |
rs150611954 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083634 | AGAAGCAGTGGAAAA[C/T]ATAAAAGTTAAAAAA | 8816 |
rs150621988 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136314 | AGAGACAGGGTCTTG[C/T]TATGTTGCCCAAGCT | 8816 |
rs150674764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141943 | AAAACAGTACTAGAG[C/T]ACATGGACTTGATCT | 8816 |
rs150686226 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052379 | TCGGCCCTCCCTACA[C/G]CAATCCCAGCTGGGC | 8816 |
rs150693591 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067739 | CCTCCCCAGTTCAAG[C/T]GATTCTCCTGCCTCA | 8816 |
rs150715754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118721 | AGGCCAGATAGCCTA[A/C]GTTCAGGTTTTAGTA | 8816 |
rs150769361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123978 | GCTGGGATTACAGGC[A/G]TGAATCACTGTGCCC | 8816 |
rs150781864 | in-del | -/A | 0.125182 | 0.216612 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081069 | AATAAGATTTAAAAG[-/A]ATATAAGAAAAAATA | 8816 |
rs150841336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056658 | TAGATGGCATCCAAC[A/C]CAGAAAACAGTGGCC | 8816 |
rs150859516 | snp | C/T | 0.00011549 | 0.00759812 | missense | DCAF5 | GRCh38.p7 | 14:69055160 | GACAGACGCTGCTGG[C/T]GAGAGGCTGCATCCT | 8816 |
rs150885518 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097091 | TGACAAGGCCACAAA[A/G]CTAGAGGAATGCTGA | 8816 |
rs150906228 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111805 | AACATGCAATGTACA[C/G]TTGTAAGTGTGAAAT | 8816 |
rs150918680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086908 | GTATAAGAGATCTCA[A/G]TGCTCAGGTACGCCA | 8816 |
rs150939479 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103303 | AAGCATATATTATAA[A/T]CTCATAATACTCACT | 8816 |
rs150941470 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138837 | ACCAGATCACTTAAA[C/T]ATTTCACAACATGAA | 8816 |
rs150994229 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144293 | TAAAGGGGCACAAGG[A/C]CAGGCGCGGTGGCTC | 8816 |
rs151066691 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075114 | TATGAAGTCTGAAGA[A/C]AAGTTTTTAGGAGGA | 8816 |
rs151076583 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126299 | AGTAGCTGGGATTAC[A/G]GACACCCACCACCAC | 8816 |
rs151130770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132575 | TTTCACTGCCTCAAG[G/T]AACATCATATATAAA | 8816 |
rs151159736 | snp | A/G | 0.000313141 | 0.0125089 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055552 | GAGGCAGCGGGAATC[A/G]TCCTCAATCCGACCG | 8816 |
rs151172229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108113 | ACTGAAATGTGCAAC[A/G]TGAATGCCACAGATC | 8816 |
rs151225760 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114047 | AGAACTCAAAACAAG[A/G]TATCATTTTTCCCCC | 8816 |
rs151300056 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079757 | TCCTGTCCCATGAAG[C/T]TTACATTCCATTAAT | 8816 |
rs180774616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061795 | AAGGCTTTTGAAAAT[A/G]TTGCAGCATACAAGG | 8816 |
rs180779542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085748 | CTCTACCTTCTCTTT[A/C]CAAAACAGAAAGTCT | 8816 |
rs180801435 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132452 | ACAGTTTGAGTTATC[C/T]TTCTTCATGAGTACC | 8816 |
rs180809780 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074090 | TGAGTTATGCCAAAA[A/G]TAGGCCCCAACAGGT | 8816 |
rs180814002 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108338 | TTGGTAACTATGACA[A/T]GAACACGTAAAGAAA | 8816 |
rs180828032 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154279 | ACTTGTCAGTTTTGC[C/T]CTTTCAAGTTAGCAG | 8816 |
rs181009537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148028 | GGCGGAGTAACAATC[C/T]AAGTCAAATGCACAT | 8816 |
rs181092634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136592 | ATGTTTTTTCACTTA[G/T]GAAAACTAATATTTT | 8816 |
rs181143628 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068497 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 8816 |
rs181169927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112752 | ATATGATGGTCAATA[C/T]TCCGATGGCACGTAA | 8816 |
rs181187352 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092012 | AAAAGGATATTTCTG[C/T]GCAGTGGCTAGAATA | 8816 |
rs181231913 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133205 | ATATGAAGGGGTACA[C/T]AGCTACCAAGAGTCA | 8816 |
rs181283554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096941 | GGAAAAAAGCAAGGG[A/G]AAGGAGGGAGACTGA | 8816 |
rs181287403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063783 | GATACCTCCTTATTG[A/C]CACGTACATATCTTT | 8816 |
rs181288784 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075644 | ACGCCACCACGCCCA[C/G]CTAATTTTTTGTATT | 8816 |
rs181299599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108802 | CCAGAAGGCATGCCC[C/T]CGACTAAAGCTAATC | 8816 |
rs181318918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140952 | CAGCCTGGCCAACAC[A/G]GTGAAACCCCGTCTT | 8816 |
rs181379045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119630 | TGAGGTGGAAGAATC[A/G]CTTGAGGTCAGGAGT | 8816 |
rs181406592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086483 | AAAAAAAGAGTAGCC[C/T]AAAATCACAACAAAT | 8816 |
rs181543045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081228 | GCAATAAAGTCCCCA[C/T]TTCCCAAAACACCCT | 8816 |
rs181546898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103349 | CATGAAGGACCAGGA[A/C]TAGAAGAGGTAGTCA | 8816 |
rs181555140 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146093 | TAATCAGTGAAAGCA[C/G/T]GTGCTTGTACCTGGG | 8816 |
rs181574644 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069485 | CTTCTTTTGTAGACA[A/C/T]GGAGTCTCATTCTGT | 8816 |
rs181574904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123715 | CTTTTTTTTTGAGAC[A/G]GAGTCTCGCACTGTT | 8816 |
rs181690046 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120263 | TAATTAAAAAAAAAA[A/T]TTTTTTTGTAGAGAT | 8816 |
rs181691410 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113604 | AGAGTTGCCCCAAAA[A/T]CTAGGTTGGGGTTTC | 8816 |
rs181697133 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141793 | ACAGGAATCAGTCCT[C/T]CTGCCAACATTATCT | 8816 |
rs181780918 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052712 | CCTTCTGACTCCTAA[C/T]AGACCTACTCAATAA | 8816 |
rs181815657 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092282 | TGGACAGTGTTTAAG[C/T]AATATAGTCATCCTT | 8816 |
rs181832533 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097382 | AATGCCTCAGAACAA[C/T]AGCTTTAAAATTTTT | 8816 |
rs181838625 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076187 | TGTGCATTGCTGGTG[G/T]GAATGACTAACGAAC | 8816 |
rs181872269 | snp | C/G/T | 0.0119091 | 0.0762411 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137385 | AACCTGGACAATATG[C/G/T]TCTCCTGATTATATC | 8816 |
rs181884867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135993 | GATATGGTTTTATAT[G/T]CTACATTGCAACTAA | 8816 |
rs181892567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, missense | DCAF5 | GRCh38.p7 | 14:69089983 | TTCTGGGTCTTCTAA[A/G]GTCCATGAAGATAGG | 8816 |
rs181896037 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111236 | TTAATCTGGTCTCTA[C/T]AGAAGTAGGATTGGC | 8816 |
rs181965123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084707 | AAATACCACTATGAG[C/T]TGCTGAACTACATTG | 8816 |
rs181978601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132255 | CCATTTTATATTCTC[A/G]CCAACAACGTACAAG | 8816 |
rs182020990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067222 | ATGAAATGAAAAGAT[G/T]TGAGTGTATTAGATG | 8816 |
rs182107886 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135033 | AGAAGAAACAAGACA[C/G]AATTGGTTAAATTCT | 8816 |
rs182149954 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053597 | CCTTGCGCGGCACAC[A/T]ACGCTCACGTCTCAC | 8816 |
rs182157411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146616 | GTAGAGGGGATATCT[C/T]TTAAAAGGTCATGAA | 8816 |
rs182164514 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103891 | GAGATTGGCTTTTTT[G/T]CAGTCAACAAAATTT | 8816 |
rs182259505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059929 | TTTTTTCTCTTTTTC[C/G]TCTGAGAACTTGGCT | 8816 |
rs182272156 | snp | A/C/G | 3.03017e-05 | 0.00389229 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152994 | GCTGGAACCGCCGCC[A/C/G]CCGCCGCTCGCGCCG | 8816 |
rs182278520 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107900 | AGCACTGTGCTAGGC[A/C]CTAGAGATTAAAGAT | 8816 |
rs182280866 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089145 | CAATCCTGATTTACA[A/G]TTAGAGAAGACTTAG | 8816 |
rs182281443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125648 | TATCAAGAAAACCTA[C/T]ATACAACATAAATAT | 8816 |
rs182284244 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109502 | AGTCAATACCTTACC[C/T]AGAGGTAACCACTAT | 8816 |
rs182285659 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065500 | GAGGGAATCAATAAA[C/T]CCAGAGACTGATGGT | 8816 |
rs182299003 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105043 | TTGTGGTTATGTTTT[C/T]TTTTTAATTATCTTT | 8816 |
rs182397554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081382 | GTGGACACACATTAT[A/C]CATAATCTTTCCCAG | 8816 |
rs182427634 | snp | C/T | 0.000164799 | 0.00907592 | missense | DCAF5 | GRCh38.p7 | 14:69054749 | GAAGTTGGTGATGCC[C/T]GGCTTGGTTGAATCT | 8816 |
rs182430033 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082315 | AAAGCATACAAATAC[A/G/T]CATACCCATAAGATT | 8816 |
rs182438815 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124432 | AGAAGATACAGAAGC[C/G]AAATCATACTTATTC | 8816 |
rs182530652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077247 | TTGCTGTGTTGCCCA[A/T]GCTAGAGTGCAGTGG | 8816 |
rs182559416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077815 | TTTAAAATCAATTTC[C/T]TAGCCTTCAAAACAC | 8816 |
rs182568398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121106 | TCTTAAAATGACAAA[C/T]AGTTTGGTGGGCTAC | 8816 |
rs182573368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121721 | AGAAGGAGTATGGTT[A/G]ATGGAAGCCATCACC | 8816 |
rs182583356 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099048 | ACGAGGTCAAGAGAT[C/T]GAGACCATCCTGGCC | 8816 |
rs182681060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093702 | CCCCCAAAGCAGTCT[C/T]CTCACCAAAGGAAGG | 8816 |
rs182698763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138974 | AACATGGTAAGACCC[C/T]GTCTTTAGAAAAAAT | 8816 |
rs182724593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148778 | TTTCATTGACCATTC[A/G]CTACCCCCATTCATC | 8816 |
rs182795468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097884 | ATGAGCCACCATGCC[C/T]GGCCACCCACTGGAT | 8816 |
rs182830583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142622 | TGTGTGTGAAAAAGT[A/G]CTTCCAAATGACTTA | 8816 |
rs182872825 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126939 | CTAAATGTAAAACCA[A/G]AACTATAAAACTCCT | 8816 |
rs182883479 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106005 | CATAGTGTGAAATAC[A/C]CAGAATAGGTAAATA | 8816 |
rs182955277 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071901 | ATAGTCCTGAAGCCA[C/T]GTTGAAGAGTAGGGC | 8816 |
rs182992562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69115886 | CTTATTTGAATATAC[A/G]ATATATAATTTTCAT | 8816 |
rs182995048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122425 | CTGACAGATGGTTTT[C/G]CCAGCCTTGAATCCC | 8816 |
rs183013130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099515 | GACCATCCAGGTCTC[C/T]ACATCTCACATGAAG | 8816 |
rs183028293 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144300 | GCACAAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 8816 |
rs183061404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143059 | AGAATCTAGGTGAGG[C/T]GAGTGCTAGCACCAA | 8816 |
rs183137958 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064566 | GGAAGATGGAAGAGT[C/T]TGAATAGGAATGGAG | 8816 |
rs183247279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116702 | GGTAAACACATTTAA[C/T]CACATTTTAAGCTAT | 8816 |
rs183392302 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093117 | TAAGTGTGATCTTTC[A/G]GGCAGTAAAGATCAC | 8816 |
rs183410877 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070939 | AGTAGCTGGGATGAT[A/G]GGTGTGCACCACTAC | 8816 |
rs183425028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083039 | TCCTTTACAACTGAA[C/T]GATTACAAACCAGAC | 8816 |
rs183448606 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114193 | AGTTTCTATCAAAAG[C/T]TTAAAAACATGCATC | 8816 |
rs183452476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138005 | GGGCTTGAAACTCAT[C/T]CCCCACAGATGAGGG | 8816 |
rs183465376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067980 | ATGTAGTTAAGCAGG[A/T]GCAGAGAAATAAAGG | 8816 |
rs183470662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139546 | GGCTTGGGCATGGTG[A/C]CTCATATCTGTAATC | 8816 |
rs183480128 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112721 | TTATCATAAGGATTA[A/C]ATGAGGTAATTATTC | 8816 |
rs183483002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136170 | ACCCAGGCTGGAGTG[C/T]AGTGGGGCAGTCATA | 8816 |
rs183486075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090147 | TAAGAAGTTGACAAA[A/G]GATAGGAAATCAACA | 8816 |
rs183561495 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087776 | CTTATTTTAAAAGAT[A/G]GAGGAAGGAAAAAGA | 8816 |
rs183579759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134558 | TCCAGATGCAAACAG[A/G]GTTAACTAGGGAATA | 8816 |
rs183611040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055899 | TGGCCCAGGGTAATC[A/C]CATACTTTCTCCACC | 8816 |
rs183771103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109067 | ATAATACAGGCCAGG[C/T]GCGGTGGCTCACACC | 8816 |
rs183806217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078936 | GGTGCAATCTCGGCT[C/T]ACTGCAACCTCCACC | 8816 |
rs183919398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106638 | GGGGCTCCCAAAGTG[C/T]TAGGATTACAGGCGT | 8816 |
rs183919739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056852 | AGAGGCTGAAGAAAC[C/T]TTCTAGATTAGCATC | 8816 |
rs183922467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058241 | TTAAATGTGGCAGCC[A/G]GGCGTGGTGGCTCAA | 8816 |
rs183926803 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083882 | TGCCCAGCCTGCCCC[C/T]GGGACTGACAGGAGC | 8816 |
rs183930142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151151 | TTTGCTCTTCAAATT[G/T]ATTTGATAAAATTTT | 8816 |
rs183932284 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106338 | TGGGATTACAGGCAT[A/G]AGCCACCGTGCCCAC | 8816 |
rs183947690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130173 | AAGGATTTGCTTTGG[A/G]TTTCCTCAAAAGCCA | 8816 |
rs183978738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69149456 | TCCTGATTTTCTCCG[C/G]TTTACTCAATATCTG | 8816 |
rs184081888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123351 | TCCAAGGAATGAGCA[C/T]TGACAGTATGCTTAT | 8816 |
rs184089452 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145300 | TGGGATTACAGGTGT[A/G]AGCTACTGCACCTGG | 8816 |
rs184109666 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128433 | TCAAGTGATCTGCCC[A/G/T]CCTTGGCCTCCCAAA | 8816 |
rs184118643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083613 | TCAAAATGGAGATGT[C/G]TCTCAAGAAGCAGTG | 8816 |
rs184121204 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123112 | AAAAATGCAGCCACA[A/C]ATGATAGCACATCCA | 8816 |
rs184122641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079686 | ATTGAATGTCTAATA[C/T]GTGTTAGGCATTGTT | 8816 |
rs184182725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094395 | GTTGTGGGCTCCAGG[A/G]TAGTAACTAACTTTT | 8816 |
rs184249826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102915 | TGTACATCATCTTAT[C/G]TACTACACTTTTATA | 8816 |
rs184263091 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052098 | CCATGCTACACACAC[C/T]CCTTCATCTCCTTCT | 8816 |
rs184263288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080797 | GACTTCACAACCAAC[A/G]TTCATATTTAATACA | 8816 |
rs184287421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144310 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCACAGC | 8816 |
rs184309754 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072392 | AAAAATAGTGGAGGT[A/G]ATAAAAAAGAACAAG | 8816 |
rs184373338 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152443 | GGAGGAAGAGTTTGC[C/T]GTCAAACTTTGTAGA | 8816 |
rs184449280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067027 | TTCCCGTCTTCCTCT[C/G]TTCTACTTTTTCTAT | 8816 |
rs184455222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089632 | TTTGATGTATATACC[G/T]AGGACTATCACAAAA | 8816 |
rs184521641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096257 | TTGTTTTCCTAATGC[A/G]CTCCTCAGTCCCAAG | 8816 |
rs184541248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140781 | AAAAGGCAAGTGACT[A/G]ACTAACCACTCTGCT | 8816 |
rs184641156 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119590 | ACTGGTGGCACACCC[C/T]TGAAGTCCCAGCTAC | 8816 |
rs184649370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075083 | GAGACTGGAAATAAG[G/T]GACATAAAGGAGTTC | 8816 |
rs184706600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146167 | GACTCTTGCTCTCTT[A/T]AGGAAATCTTAGCTA | 8816 |
rs184759451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073768 | AGAGAATAGTCCTGG[A/G]GAGAAGAAGGATTAT | 8816 |
rs184768815 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118150 | CTACCTCCATGGGGG[A/G]ATTCCCGAATGTCCC | 8816 |
rs184777416 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140191 | AGAATCTCTTGAACC[C/T]GGGAGGCGGAGGTTG | 8816 |
rs184787082 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095537 | TTATTTTGTTTTGTT[C/T]TGTTTTTTTAAGTAC | 8816 |
rs184846606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066368 | TCTCCAACTCCTGAC[C/T]TCATAATCTGCCCGC | 8816 |
rs184864510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109867 | TGGGTCATGGAGTTA[C/T]GGTGTTTAGCTTTAG | 8816 |
rs184926603 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053606 | GCACACTACGCTCAC[A/G]TCTCACTAGAAAGGA | 8816 |
rs184975033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084447 | AACTTTTGCCAACAC[A/G]TAGACAGACGATGCT | 8816 |
rs184982869 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135649 | TCAAGGAAAATAATT[G/T]GCAGTATTTGTAGCC | 8816 |
rs185021215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131136 | AGTATGATACAATTA[C/T]ACAAAAACATACACA | 8816 |
rs185093965 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155256 | GGCAGTGTATAATAC[A/G]CATCCTCCTCTGCCC | 8816 |
rs185105379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059768 | CTCCAGAGCTTTTTG[C/T]TTTCCTTCTCACTAT | 8816 |
rs185123680 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107717 | TAAGGATTTATTCCT[A/G]AGATACAACATTTGG | 8816 |
rs185213762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138291 | GGCATCTGGATTTGC[A/C]AAGAATTCCTCCTCC | 8816 |
rs185218905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062756 | ACTCACCCACTGCAA[C/T]TCCATTGTCAATGAA | 8816 |
rs185252950 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132973 | GATTAATGAGATAGA[A/G/T]CTGTGTAAAAGACTT | 8816 |
rs185262617 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085804 | TAAAACATTCACGCT[C/G]TAAAAAAGACATACA | 8816 |
rs185268078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108367 | AAAATCAAGAAAACA[A/G]GAGAAAGCATCCTCT | 8816 |
rs185321862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135946 | TCAATGGATTTTAAT[A/G]TAACAATGTAACAGG | 8816 |
rs185370559 | snp | C/G/T | 0.000131821 | 0.00811753 | missense, synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054757 | TGATGCCCGGCTTGG[C/G/T]TGAATCTCTAGCGTG | 8816 |
rs185375542 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082651 | TAACCATTAGCCCCC[C/G]TCCATGGGCTTCAGT | 8816 |
rs185398187 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126035 | CCGGCAATGAATAAG[A/T]GGAATTTGAAATATA | 8816 |
rs185419036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105250 | CCAAACGGCTATCAT[C/T]AGATGAATGGATAAA | 8816 |
rs185434747 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148380 | GACTACAATCATCAA[A/G]TATAAGCTAGTCTTT | 8816 |
rs185457714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110946 | TAATTTTAATGAAAT[C/T]CAATGTGTCAATTTT | 8816 |
rs185467119 | snp | A/G | 0.0130921 | 0.0798413 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153922 | AGTTGATGAAGTCCC[A/G]AGAAGCACGAGGTAC | 8816 |
rs185474208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108221 | CACTCTGTGCCAAAA[C/T]AGTGCCAGGTGCCGG | 8816 |
rs185587351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132264 | ATTCTCACCAACAAC[A/G]TACAAGAGTTCCAAT | 8816 |
rs185772691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085071 | GACATTCAGTCTCAG[C/T]TTGAGAAATTGATTC | 8816 |
rs185790907 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081787 | GTGTGTTTGTGGTGC[A/G]TGCTTACACAGGATT | 8816 |
rs185828100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124610 | TTTCAACTATGAGTT[A/C]TCTGGCCTAGGATAG | 8816 |
rs185921801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097162 | AGAGGGTTTGAAAAG[A/C]AAAATCATGATTTAG | 8816 |
rs185932939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120113 | TTTCGAGACAGGATC[C/T]TGCTCTGTTGTCCAG | 8816 |
rs185942540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146881 | TAAAATGTCTATACT[A/G]TGAAAGCTTTTCAAA | 8816 |
rs185947825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075726 | TGACCTCAGGTGATC[C/T]GCTGGCCTTGGCCTC | 8816 |
rs185952713 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104713 | ATACCAAAAATTAGC[C/T]GAGTGTAGCAGCGGG | 8816 |
rs185960271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142952 | AATCAGACTAAAGTA[A/G]GGAGTTAAACCCAGT | 8816 |
rs185967980 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141401 | GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC | 8816 |
rs185970612 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098879 | GCCTGGCCGACTGAG[C/T]GAGACTCTGTCTCCA | 8816 |
rs186108064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121413 | AAAGGCAGGTTTGAG[G/T]ATGACTCCAAGATCA | 8816 |
rs186255786 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112763 | AATACTCCGATGGCA[C/T]GTAATGCTTAATAAA | 8816 |
rs186261877 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077640 | GCCTCAGCCTCCCAA[C/T]GTGTTGGGATTATAG | 8816 |
rs186265938 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092463 | CTCTACAAAAAAATT[A/T]AAAAATTAGCCAGGC | 8816 |
rs186271090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068659 | GCCGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 8816 |
rs186277840 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113635 | TAGGCAGCTGTGCTC[A/C]AGAGACAAATTATCT | 8816 |
rs186278125 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069895 | CAAAGTGCTGGGATT[A/C]CAGGCATGTGCCACT | 8816 |
rs186283451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124309 | TACAAATAACTTTTT[C/G]AGTCCCTCCTTTCAA | 8816 |
rs186367654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097510 | TGTACTTTCTATTCT[A/G]TATTTTTTATTTAAG | 8816 |
rs186379224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141881 | ACTCCTACATAATCC[C/T]AGCCCTTTGGAATAT | 8816 |
rs186393878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120785 | AGGTCTTGGGTATAT[A/G]AAAAGAATAAGATTC | 8816 |
rs186433285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092042 | AATGAGGGTAGCAAC[A/G]CTTCCTTCGTTACTT | 8816 |
rs186445898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137121 | TGGGTGGGAGGCCTA[C/T]CTTGTAAGTACCATA | 8816 |
rs186597547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133462 | CCCAATTTTTGGCCC[A/G]GGGATAAGTTAAGGT | 8816 |
rs186617697 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087266 | ATTAAGAGACTCGCT[A/C]ACTGAGTATGTAGAG | 8816 |
rs186652015 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093231 | TGAATTACTGGCAGG[A/G]AAGTGAAGTATATAT | 8816 |
rs186678413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114977 | AGTGCCCCACTCCAG[G/T]TGCCAGCTATTCATT | 8816 |
rs186682199 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057642 | TTTGAGCTCTGGAAT[C/G]TATTAAGCTGAGGTA | 8816 |
rs186684513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083667 | TCCCCAGAAATCCAC[C/T]GTATTAACCAATGGA | 8816 |
rs186772359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137397 | ATGCTCTCCTGATTA[C/T]ATCACAAATACGCTC | 8816 |
rs186796041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089207 | ACGTACTCAAGATTT[A/C]CTTCAACAAATTTTT | 8816 |
rs186802826 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109611 | ATTCAATATTATGAC[C/T]GTGAGATTCATCCAT | 8816 |
rs186810126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064430 | CCTCAAAAAGAGGGG[A/G]GATGTGGGGGGATTT | 8816 |
rs186816003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065995 | GAATCGCTAATAATG[A/G]GTACCCATAAATAAA | 8816 |
rs186828211 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108894 | CCAAAATTTCTAGGT[A/C]CACCTGACTCTTCTC | 8816 |
rs186831797 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135168 | TTTTCGCAATAACAC[C/T]ACAATGTTATTTGCC | 8816 |
rs186935720 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103483 | AGAAATGTACAAGAA[C/T]GTCCTGTGCATCCTT | 8816 |
rs186953198 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052724 | TAATAGACCTACTCA[A/G]TAAGAATCTGTTACC | 8816 |
rs187115253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076337 | AGAGATATCTGTATA[C/T]CCATTTTCATAGCAG | 8816 |
rs187121116 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106727 | TTTTTAAGAAGAAAA[C/T]GTCAACATTTGATTT | 8816 |
rs187127321 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081365 | AAATGAACATGAGTT[A/G]TGTGGACACACATTA | 8816 |
rs187135448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151210 | TGTCTGAAAGATCAG[A/G]TTTCTTCAGAGGATG | 8816 |
rs187170653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130779 | TTAGATACAGAGCTT[A/G]GGGTTTCATCTTTGA | 8816 |
rs187255759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078452 | AATTCCAATTCTGGG[A/T]ATATATCCAAAAGCA | 8816 |
rs187267644 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121861 | CTTTAAAAATGAAAT[C/T]GAATAGAATAAAAAA | 8816 |
rs187274001 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143637 | TAATTTGGTAGGCGC[C/T]GGGGAGTGCTGCAGA | 8816 |
rs187278485 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099114 | AAAATTAGCTGGGCA[A/T]GGTGGTCCACACCTG | 8816 |
rs187372504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073493 | TCCTAAATCAGTAAA[G/T]AAAGCAGCAGGGGGC | 8816 |
rs187402149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139645 | ATGGTGAGACCCCGT[C/T]TCTACTAAAAACACG | 8816 |
rs187404322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094915 | TACAGGTAGCTTTCA[A/G]ACCACACTGTGAGAA | 8816 |
rs187416052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148932 | ACTTTCCACACCACA[C/T]TGTGCCTCCACATTC | 8816 |
rs187419760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116860 | ACCAAGTATGGTAGG[C/G]TTATTATGCTTTTAA | 8816 |
rs187745637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071428 | CTCTCAGCACTCGGC[A/G]CGCACATGAAACACA | 8816 |
rs187750038 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144302 | ACAAGGCCAGGCGCG[A/G]TGGCTCACGCCTGTA | 8816 |
rs187750766 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106459 | CTGCAGCCTCAACCT[C/T]CTGGGCTCAAGCGAT | 8816 |
rs187828118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109340 | CAAAACTCTGCCTCA[A/G]AAAAAAAAAAAAAGA | 8816 |
rs187836136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064630 | AAATCTTTCAGGCAG[C/T]TATTAGATAGGTGGT | 8816 |
rs187842244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088376 | TCTCTAATAGCTCTA[C/T]AATTAGAATTCATCT | 8816 |
rs187909085 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072044 | GCAATACAAGGCACA[C/G]CTGGGGGTGTCATTA | 8816 |
rs187950171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116134 | TGCCTAAAACTCACC[C/T]TGTCTACAGTCCAGA | 8816 |
rs188079902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135689 | ATTCAAGCTTTCAAG[A/T]AAAAATAAAAATTTT | 8816 |
rs188196224 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093899 | CCTGCAGAGAAATGC[C/G]CTTATAATGGTCCTA | 8816 |
rs188206921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112738 | TGAGGTAATTATTCA[C/T]ATGATGGTCAATACT | 8816 |
rs188213532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136253 | CCAGAGTAGTTGAGA[C/T]TACAGGTGCACATCA | 8816 |
rs188219097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139014 | AAATTAGTCAGGTGT[C/G]ATGGCACGTGCTTGT | 8816 |
rs188263852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089531 | GTCACAAATAATAAA[C/T]TAGTCAAATCTAAAT | 8816 |
rs188290282 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051083 | CTTCACTTGCCCCAA[A/G]CCAACAACTTAACTC | 8816 |
rs188333280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079876 | CAGTGGTGACAAATA[C/T]TACAGAGGAAAATTA | 8816 |
rs188379963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106213 | AGGGGCCCACCACTA[C/T]GCCCGGCTAATTTTG | 8816 |
rs188380508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110136 | AGTACCTGTTCAACA[C/T]TTCTGCTCATTTTTT | 8816 |
rs188557084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066938 | AAAGCTGAAAGCAAT[A/G]TGGTCAAGATTTCTT | 8816 |
rs188561850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055943 | CTTTTAGTTTCATCT[A/G]TTAGTAGTTGGACAT | 8816 |
rs188631728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083900 | GACTGACAGGAGCTT[C/T]TGAGGATACTTCATT | 8816 |
rs188642434 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058655 | CAAGGCAGGAGGATC[A/G]CTTGAGCCCAGGAAT | 8816 |
rs188674226 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083263 | ATTTTTCTGAGATGA[C/T]TGTTTATAGCTTTTA | 8816 |
rs188734248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122811 | CAATCTTCTTGATAT[A/G]ATCTCATTGATTGTG | 8816 |
rs188740692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079546 | GTCCTGCAGAATTCA[C/T]TATGGCATTTCACGG | 8816 |
rs188785422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103074 | GACTTTTGTCATACA[C/T]GTGGGTCCATTATTG | 8816 |
rs188793541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081113 | ATGAAACTCACTTCG[C/T]ACAGCCTTTTATCTT | 8816 |
rs188795662 | snp | A/C | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052565 | AACCGAGTGACTGCA[A/C]CGCTGAAAATCTGTT | 8816 |
rs188799799 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145523 | GAAAATAAAAAAAAA[A/T]ATTTTAATTTCCCAT | 8816 |
rs188816709 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123714 | TCTTTTTTTTTGAGA[C/T]GGAGTCTCGCACTGT | 8816 |
rs188892088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128547 | AGAAAAAAAACAAGA[C/T]TGCAGGATGGGCTGG | 8816 |
rs189021531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134599 | AAATTAGGAGAATGT[A/G]ACTGTTTTAACAAAG | 8816 |
rs189025999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099581 | ATTCATCCATGTGCT[A/G]ATCATGTAAGGATCC | 8816 |
rs189124187 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097211 | CTTATGCAAACAATT[A/G]AAAACAAGAGAAGAG | 8816 |
rs189144224 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075796 | GCCTAAACATACTGA[A/T]TTTTAATATATCTAT | 8816 |
rs189160077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120180 | TCTTGACCTCCTGTG[C/T]TCAAGCAATCTTCCC | 8816 |
rs189167361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141696 | GGCAGGCAGGTGACG[C/T]AGAGTTACCTAATGA | 8816 |
rs189178574 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150285 | AAAGAAGGCTGGAAC[C/G]CAGGAAGTACTGATG | 8816 |
rs189203496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100902 | ATTACAAAATAGAAA[G/T]TTCAAACTACAAAGA | 8816 |
rs189206974 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068344 | TATCTGCTAAAATGA[A/G]GTTTGGTAAGTAGAT | 8816 |
rs189241641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144432 | AAAAAATTAGCTGGG[A/C]GTGGTGGCGGGTGCC | 8816 |
rs189277054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067182 | ACTGTGCCTAGCACA[C/T]AGTAAGGTTTTTAAT | 8816 |
rs189304982 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135991 | TCGATATGGTTTTAT[A/C]TTCTACATTGCAACT | 8816 |
rs189315565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089764 | CCCCCCAGGGGACAA[C/T]GTCTGGAGACATTTT | 8816 |
rs189323634 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111104 | CATCAGAGCATGAGT[A/C/G]CCTTTTCCAGCCTTT | 8816 |
rs189339703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074025 | TTCTAAATTCTAGAA[A/G]AGGAAAAGCCCTTTT | 8816 |
rs189426007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060440 | ATGTGTGCTGCAATG[A/G]AAGTCAGCTCTGATC | 8816 |
rs189427761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118363 | GGTACCGAGGGTGCC[A/G]TCTTTTCCATTTCTA | 8816 |
rs189429688 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085652 | ATATAATATTTTAAT[G/T]TTAAATATCCCTCCC | 8816 |
rs189460193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140197 | TCTTGAACCCGGGAG[A/G]CGGAGGTTGCAGTGA | 8816 |
rs189467503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108306 | GGAAGTTTTCCCTGA[C/T]GGATTACCATTTGAT | 8816 |
rs189491169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123245 | ACAGTATGTAATCCA[C/T]TTGCATAAAACAAAA | 8816 |
rs189520050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090963 | CCATTTGTCTTTCCT[C/T]GGCTTGGTGACCCAG | 8816 |
rs189552692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119622 | AAGGAGGCTGAGGTG[A/G]AAGAATCGCTTGAGG | 8816 |
rs189560911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075486 | ATGTAACAATAAACA[C/T]ATTAATTTTTTTTGA | 8816 |
rs189671833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140908 | GATCACCCCCGCCTA[A/G]GGACTGAACTCTGTC | 8816 |
rs189749616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138634 | GAGTTTAATCCTGAT[G/T]GTACTACTCACTAGT | 8816 |
rs189755621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137303 | TTAGTGGATGATGCA[C/T]TGCCAGGTACTTCCA | 8816 |
rs189771831 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082106 | GATTGAAAACTTTGT[A/G]ATATGCTCTCTAGAT | 8816 |
rs189780129 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053787 | TTTTTCCTTTCCTCT[C/G]TATTCACTAAACAAT | 8816 |
rs189823912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096415 | TACAGATGAATTCAG[C/T]ATACTTTTTGAATCT | 8816 |
rs189911739 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077735 | ATCGAACATCCCCAA[A/G]AAGTGTAAGTCCAAC | 8816 |
rs189917737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133157 | CAACCCCACGAAGTA[C/G]GAATTCACATGAAAC | 8816 |
rs189924045 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086266 | CGGAGGCTGTGGCAC[A/G]AGAATTGCTTGAACC | 8816 |
rs189932303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108467 | ACCTTATGGAGAGAC[A/G]GAAATGGGTATGAAA | 8816 |
rs190034308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059882 | GCAGTGAGCTCCATA[A/G]TTCAGTCTGGATAAC | 8816 |
rs190044599 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152503 | CACTTTCAGGGCAGG[C/T]ATCAGGAGAGATCAC | 8816 |
rs190055514 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107853 | AACACTATATATTCA[C/T]TCAATATTTACTAAG | 8816 |
rs190207495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124362 | ACTTTTACTTTCTAC[C/T]TTCCTATACTGCTTG | 8816 |
rs190257979 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126485 | TTTAAGATATCAGTT[C/T]TTCCCAACTTCATCT | 8816 |
rs190266252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084456 | CAACACGTAGACAGA[C/T]GATGCTCTTTTCTGC | 8816 |
rs190271136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082661 | CCCCCCTCCATGGGC[A/T]TCAGTTTTTGTATGT | 8816 |
rs190272953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105662 | AAGCCTGATGCTTTG[C/T]TTCCTCTCCTCCTGC | 8816 |
rs190293785 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148549 | AAAATACAAAAATTA[A/G]CCAGGTGTGGAGGCA | 8816 |
rs190310661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132053 | ATCCACTGATGGACC[C/T]TTGGGTTGCTTCTAC | 8816 |
rs190363297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081381 | TGTGGACACACATTA[A/T]CCATAATCTTTCCCA | 8816 |
rs190439636 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146258 | GGACAACTTTTTGAT[G/T]TATTAATAACAATGT | 8816 |
rs190508872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095726 | GCACAACATAGGGAA[A/T]TGAAAAAGCTTCCAA | 8816 |
rs190514938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132329 | GCTTGTTTGGATAAT[A/G]GTCATCCTAATGGGT | 8816 |
rs190621233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103630 | GCATTCATTTGTGTT[A/G]GGTGAATGTGATAAC | 8816 |
rs190626408 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053443 | TGTAAACAGGGTGAG[A/G]TGGCAAAAAGTACAA | 8816 |
rs190701556 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115122 | GCAGAGAACACTGCA[C/G]ATGAACACAGTTGTC | 8816 |
rs190771879 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154220 | AGTACTTTTCCTGGA[A/C]GCTATCCTCTGTCAT | 8816 |
rs190841032 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69092875 | ACTTTGGTTAATATA[C/T]AGAACTTCATTTATC | 8816 |
rs190845453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114018 | AACTATAAAACCTTA[A/C]CCATAATTGAAGAAG | 8816 |
rs190859548 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070922 | TCTGCCACAGCCTCC[C/T]GAGTAGCTGGGATGA | 8816 |
rs190864606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147631 | TTATAATGATCAATA[G/T]GGTCAGAGACCCATT | 8816 |
rs190872986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071733 | GACAAAATTTTCCTC[A/G]TCTAAGCATTCAAAG | 8816 |
rs190878247 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137617 | ACTACACCCAGCCAC[C/T]CACCAGCAGATGTAA | 8816 |
rs191027823 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121666 | TCCAGTGGGAAAATC[C/T]GCAGCTCAGAAAAGA | 8816 |
rs191107339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125350 | AAACTGAAGGACCAG[A/G]ACAGGACTGCCTGAA | 8816 |
rs191113645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093478 | GTGAAAAAAGAGCTA[C/T]ATATTACCAGAAGAG | 8816 |
rs191186600 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142327 | ATCAGGTAACTAAAG[C/T]GACAAACTACTACTG | 8816 |
rs191188872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088860 | TAGACTCATCAAAGA[A/G]TATACATGTCAGTCC | 8816 |
rs191190375 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109374 | AACATAATATGATAA[A/C/T]ATGCACTAATTCTAA | 8816 |
rs191198400 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065341 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 8816 |
rs191221902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134907 | TTAAAAATATAAAAA[A/T]TATTCACACCCATTG | 8816 |
rs191257142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142981 | GTGGGAGTTAGTCAC[A/G]TGGTTACGTATGGAA | 8816 |
rs191267464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098941 | AAAAGAAAAACACTG[A/C]CTTAAAACGTTTTTA | 8816 |
rs191327723 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092165 | TTGAAAGAAGAGACA[C/T]ATTAAAATAATGATT | 8816 |
rs191337601 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106472 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTCAG | 8816 |
rs191345496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057970 | TAAATGAGAATGATA[C/T]CAAAGCCCATACCCA | 8816 |
rs191347544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083842 | AATAATGTTGAGAAG[A/C]CAGATGATGAAGATG | 8816 |
rs191367056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129468 | GCGCTAAACAGCTGT[A/G]CCCAAGCCTCTGATT | 8816 |
rs191409029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063164 | GAATTAGAGAGTGGG[C/T]CTTAAAGATACCATG | 8816 |
rs191556685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113390 | TTATCCTTTTGGAGT[C/T]AAGGGTCTCTATGAG | 8816 |
rs191564602 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068773 | CTAAAAAAGGTATCC[A/T]AGCCTCTTAGCATTT | 8816 |
rs191638479 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052047 | TCACTTTCCCACTCC[C/T]CCAGTAAAAGTCCAG | 8816 |
rs191640345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064562 | CTTTGGAAGATGGAA[C/G]AGTTTGAATAGGAAT | 8816 |
rs191654194 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101825 | CAACTGTAACACAAT[A/G]GGTAAGTATTTGTGT | 8816 |
rs191664140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109655 | TTTATAGTTTGTTGT[G/T]TATTTATGTTTGTGT | 8816 |
rs191667160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108901 | TTCTAGGTCCACCTG[A/C]CTCTTCTCGTTCTCT | 8816 |
rs191671031 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080744 | TGGTTACCCAAAATT[C/T]CTATGTTTCATATTT | 8816 |
rs191671201 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135345 | CCACGTTCACTCAGG[A/C/G]GTGCCTTGATGAAGC | 8816 |
rs191750453 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134432 | TGACACTCCTTATAT[A/T]TAACAAAAATCAAAA | 8816 |
rs191785443 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152399 | CCCTCCACATCCCCA[A/G]AATGCCCCCAGCACC | 8816 |
rs191801008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131087 | TTGTCCTAATCTTTC[A/C]AACCTTGTTTTAGGT | 8816 |
rs191823546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128148 | TATAGATGCATACAC[G/T]ATACTATTCTACTTT | 8816 |
rs191839324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072382 | ACTTAATTACAAAAA[C/T]AGTGGAGGTAATAAA | 8816 |
rs191934448 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107269 | TGAGAAGGAATGGAC[A/G]CAAGCAATCTCTGGC | 8816 |
rs191962786 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148706 | TTGCCCCCACCGCCC[A/C]AAAAAAAAGTAATGT | 8816 |
rs191980635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087717 | TGTGAATGTATCTAT[C/T]ACAGCATCAGGCATA | 8816 |
rs191998695 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144196 | GGCAAATAAGACATG[A/T]AAAGTGCTTAGCAGA | 8816 |
rs192013284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099295 | ACACACACACACACA[C/T]ACACAACTAACAAAG | 8816 |
rs192067771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097814 | CTGGTCTTGAACTCT[A/G]CTGACCTCAAGTGAT | 8816 |
rs192154249 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149227 | CTTAGTAACTTGACT[A/C]AAGTCACAGATTAAA | 8816 |
rs192180336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078585 | CAGCCTTAACAAGGA[A/T]GGAAATTCTGACACA | 8816 |
rs192246191 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118448 | TAGTCAACTTTCAGG[C/T]TAAAAAAAAGGTACT | 8816 |
rs192266127 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150494 | GCCCAAGGATAAAAG[C/G/T]AGTAATAACTGGTAA | 8816 |
rs192333090 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073658 | CCCTGTCTCTTACAA[A/C]AAAAAGAAAAGAAAG | 8816 |
rs192350235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117507 | GGTGGGTATGGCAGT[A/G]GCACTAAGGCTGGTA | 8816 |
rs192358950 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139714 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGGGAAT | 8816 |
rs192362161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095457 | CCAAAAGACCTAGGG[C/T]GAAAAGCAAGAACAC | 8816 |
rs192434441 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076550 | AAAAAGACAGATATT[G/T]TATGACTCCATTTAT | 8816 |
rs192473916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120830 | GAACTCCAATTGGAC[C/T]TGAGAACAGTCCAAC | 8816 |
rs192549912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089276 | CAATGATGAATTAGC[C/T]ACATTTCTTAGTCCC | 8816 |
rs192672629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095826 | ACCAACAAGATTTTC[C/T]AAAGACCACTGGCAT | 8816 |
rs192692268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140736 | CTGGCATGTTCATAA[C/T]GGTTTCAGCCTTTTT | 8816 |
rs192783394 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093947 | CTTGCATACAGAAAA[G/T]GAATGACAGGATTGT | 8816 |
rs192794492 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139537 | AGAAAAGGAGGCTTG[C/G]GCATGGTGCCTCATA | 8816 |
rs192803828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058829 | CAGTGAGCCATGATC[A/G]TGCCACTGTACTCCA | 8816 |
rs192837940 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066102 | ATTTCTCTGGGCCAT[A/C]TGCTTTGGTTGGCTT | 8816 |
rs192856456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066971 | TGTCTTGGTCTAATA[G/T]CAATTTATCAATCAT | 8816 |
rs192861806 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144504 | ATGAACCTGGGAGGT[A/G]GAGCTTGCAGTGAGC | 8816 |
rs192876828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110422 | AGGCACACAACACCA[C/T]GCCCCACTAATTTTC | 8816 |
rs193001836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084070 | TCAGTGGTAAAACCC[C/T]AGCTTTTCTCATCCT | 8816 |
rs193008842 | snp | C/G | 0.000265265 | 0.0115136 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116527 | TATAATCAGTTCACT[C/G]CAGGTACCTGTGGGC | 8816 |
rs193020925 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083506 | AATCTGACCCTGTCC[A/G]AAACTCAAAATACAG | 8816 |
rs193063289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089548 | AGTCAAATCTAAATA[A/G]AGAAAAATCAAAAGC | 8816 |
rs193073234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135712 | AAAATTTTGGAAAAA[C/T]TGTATTCACCATGGT | 8816 |
rs193101624 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144304 | AAGGCCAGGCGCGGT[A/G]GCTCACGCCTGTAAT | 8816 |
rs193151826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099753 | TTTGAGGCCAGCCTG[G/T]GCAACAAAGTGAAAC | 8816 |
rs193206494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056492 | GTGCAAGGTAATTAA[A/G]CTGTCACTGCAAACG | 8816 |
rs193211574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106217 | GCCCACCACTACGCC[C/T]GGCTAATTTTGTATT | 8816 |
rs193298260 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122886 | GTAATAGGATCTAGA[C/G]AGAATATGGCTCAGC | 8816 |
rs193300241 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079612 | CTGCCTGGGATACTG[C/T]TGACTATAAGGACAG | 8816 |
rs199498666 | snp | C/G/T | 3.2961e-05 | 0.00405951 | missense | DCAF5 | GRCh38.p7 | 14:69054153 | TCTGCCCGTTATTGT[C/G/T]AGGGTGAGGGGGACG | 8816 |
rs199512862 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118287 | CTCACTGCTGGGAGA[C/T]AAGAGAGCAAGACAG | 8816 |
rs199534752 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128195 | TTTTTTCTTCTTCTT[-/C]TTTTTTTTTTTTTGA | 8816 |
rs199552564 | snp | A/C/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119720 | AAAAAAAAAAAAAAA[A/C/G/T]TAGGGGGGAAACAAC | 8816 |
rs199624200 | in-del | -/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154395 | GGAAAATAATAATAA[-/T]TTTTTTTAAAAAAAA | 8816 |
rs199658863 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099790 | TCTACAAAAAAAAAA[A/T]ACAAAAATTAGCCGA | 8816 |
rs199758443 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109353 | AAAAAAAAAAAAAAA[-/A]GATACAACATAATAT | 8816 |
rs199823757 | snp | A/C/G/T | 0.0600356 | 0.162522 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053815 | AATTTTTTTTTTTTT[A/C/G/T]TAAGGCTACTTTTGT | 8816 |
rs199870726 | snp | A/G | 0.000148494 | 0.00861539 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055333 | GTAGCCTGAGCGCTC[A/G]CTGACCCCAGCGTGC | 8816 |
rs199891640 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122875 | TGACTCTTACAGTAA[A/T]AGGATCTAGACAGAA | 8816 |
rs199920890 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099788 | TCTCTACAAAAAAAA[A/C]ATACAAAAATTAGCC | 8816 |
rs199939004 | snp | A/T | 0.00199808 | 0.0315444 | missense | DCAF5 | GRCh38.p7 | 14:69054650 | AAGGAGGTCTCTCCA[A/T]CTTTGTTATTTGAGT | 8816 |
rs199970007 | snp | A/G | 4.98749e-05 | 0.00499349 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116347 | AAAGTTTTAACACCT[A/G]TGAATAAAGGGGGCT | 8816 |
rs199987533 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135372 | AAGCAGTAAAAATAA[C/T]TGTATCAAATTTCAA | 8816 |
rs200011527 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058553 | ATATATATATATATG[G/T]CTAGACATGTCTCAT | 8816 |
rs200017545 | snp | A/G | 0.0329347 | 0.124027 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152726 | GGGGAGGCTGGGAGG[A/G]TGCGGGGAGGCGCGG | 8816 |
rs200031103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109434 | TATACAACCATGAAA[C/T]TGCCACCCAGATCAA | 8816 |
rs200134644 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058476 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 8816 |
rs200156447 | snp | A/G | 0.000131794 | 0.00811661 | missense | DCAF5 | GRCh38.p7 | 14:69054515 | CTGCAGCCTTCAGGT[A/G]GCAGGTCCTGGTTCC | 8816 |
rs200164341 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053647 | TTATTTTTTTTTCCC[C/T]TTTCTTAACACAGCA | 8816 |
rs200180810 | in-del | -/A | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154402 | ATAATAATTTTTTTT[-/A]AAAAAAAAAGATCGG | 8816 |
rs200205620 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060946 | GAAATAAAATAATCA[C/T]AATTTTTATTTTTTT | 8816 |
rs200236619 | snp | A/G | 8.23689e-05 | 0.00641698 | missense | DCAF5 | GRCh38.p7 | 14:69054770 | GGTTGAATCTCTAGC[A/G]TGGAAGTGCTCCGCT | 8816 |
rs200330514 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081764 | AAAATGTGTGTGTGT[A/G]TGTATGTGTGTGTTT | 8816 |
rs200442369 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117273 | CACTTACCAAGCCCA[C/T]AGTGACTCGACCACA | 8816 |
rs200458341 | snp | G/T | 0.000281054 | 0.0118511 | missense | DCAF5 | GRCh38.p7 | 14:69054026 | GTCTCACAGGCCATT[G/T]CAGACCCGCAACAAT | 8816 |
rs200483812 | snp | C/G/T | 4.95555e-05 | 0.00497752 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69075400 | GAAGTCATCAGAGCC[C/G/T]GAAAGGATATACTGT | 8816 |
rs200568900 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107072 | AATTAAATAATTAAA[A/T]AAGAAAGTCCATTTG | 8816 |
rs200578914 | snp | A/C/T | 1.64806e-05 | 0.00287054 | missense | DCAF5 | GRCh38.p7 | 14:69054189 | GTAAGCGTCCATTGT[A/C/T]GTGGTTGGCACAGAT | 8816 |
rs200580853 | snp | C/G/T | 6.59026e-05 | 0.00574 | missense, synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054508 | GTCCTTGCTGCAGCC[C/G/T]TCAGGTGGCAGGTCC | 8816 |
rs200580922 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132178 | TGAAATTGCTGGATC[A/C]ATATGGTAATTCTAC | 8816 |
rs200589279 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099791 | CTACAAAAAAAAAAT[A/T]CAAAAATTAGCCGAG | 8816 |
rs200601552 | snp | A/G | 1.648e-05 | 0.0028705 | missense | DCAF5 | GRCh38.p7 | 14:69054092 | TCACGGTCAGTGTCT[A/G]AGTGTCCTGGGGAAG | 8816 |
rs200613077 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097588 | ATTATTATTATTTTT[A/T]TTTTTTTTTTTTTTT | 8816 |
rs200677268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070784 | CTTCCTCTAATTTTT[A/C]TTTTTCTTTTTTTTT | 8816 |
rs200682831 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086618 | GCGTGCATGGAGTTA[-/T]TTAAAAAAAAAAAAA | 8816 |
rs200705569 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098823 | GAATGGCATGAGGAG[G/T]CGGAGCTTGTAGTGA | 8816 |
rs200738592 | in-del | -/A/AA | 0.0275645 | 0.114116 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071309 | TGGAGTTTGTATAGC[-/A/AA]AAAAAAAACAAAGAC | 8816 |
rs200767759 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058537 | AAAAGAAAAAAAATA[C/T]ATATATATATATATG | 8816 |
rs200862680 | snp | C/T | 0.00102229 | 0.0225854 | missense | DCAF5 | GRCh38.p7 | 14:69055562 | GAATCGTCCTCAATC[C/T]GACCGTCGAGGTCTC | 8816 |
rs200876392 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126251 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 8816 |
rs200882187 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131261 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTAACTGT | 8816 |
rs200888922 | snp | C/T | 0.000709354 | 0.0188195 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122192 | AACCACAGTGACGTT[C/T]CCAAGGTAGAATCTC | 8816 |
rs200957480 | snp | C/T | 0.000272183 | 0.0116626 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091644 | AAAGAAAAGCATAAG[C/T]GTGAGATGCAGGAGG | 8816 |
rs200970711 | snp | A/G | 0.00199806 | 0.0315443 | missense | DCAF5 | GRCh38.p7 | 14:69054362 | AGCTTCTTGGTTTCA[A/G]AAGGGTGCTCTACAG | 8816 |
rs201064574 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120822 | GTCCTTGAGAACTCC[A/C]ATTGGACTTGAGAAC | 8816 |
rs201086749 | in-del | -/GTGT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081760 | ATAGAAAATGTGTGT[-/GTGT]GTGTATGTGTGTGTT | 8816 |
rs201102277 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142131 | AGATCCTGTCTCTAC[-/A]AAAAAAAAATTTTTT | 8816 |
rs201132415 | snp | A/G | 9.9208e-05 | 0.00704231 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055579 | ACCGTCGAGGTCTCC[A/G]GTACATCCTGGCTGC | 8816 |
rs201133127 | in-del | -/AT | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113448 | TAGAAAAAATATGAC[-/AT]GTGTTCACTCAGATA | 8816 |
rs201208544 | snp | C/T | 0.00233112 | 0.0340606 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122403 | TAAAACAGCTGACAT[C/T]GCAAGGCTGACAGAT | 8816 |
rs201302750 | snp | A/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077615 | ACTTCTGGGCTCAAG[A/G/T]GATCCTCCTGCCTCA | 8816 |
rs201378128 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076130 | CAAAAAAAAAAAAAA[-/A]TTGACAAGTATTGGC | 8816 |
rs201402935 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081768 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTTTGTGG | 8816 |
rs201460846 | in-del | -/TC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141352 | TGGGACCTTTTTTTT[-/TC]TTTTTCTTTTATTAT | 8816 |
rs201467372 | snp | C/G/T | 3.29625e-05 | 0.00405958 | missense | DCAF5 | GRCh38.p7 | 14:69054167 | TGAGGGTGAGGGGGA[C/G/T]GAGGGTGTAAGCGTC | 8816 |
rs201470616 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060997 | CAAAGTCATTTTAAT[-/A]AAAAAAATTGAGGAT | 8816 |
rs201512356 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132179 | GAAATTGCTGGATCC[A/C]TATGGTAATTCTACT | 8816 |
rs201542551 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110942 | TTCTTAATTTTAATG[-/A]AATCCAATGTGTCAA | 8816 |
rs201561102 | snp | A/T | 0.00172648 | 0.0293302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091670 | GGAGGCAGACAGCAT[A/T]TACCTGGTCACGATC | 8816 |
rs201576126 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099792 | TACAAAAAAAAAATA[A/C]AAAAATTAGCCGAGC | 8816 |
rs201586030 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145668 | TATTTTATAAGAATA[A/T]TTTTTTAAACAATGT | 8816 |
rs201621919 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118262 | CTTCATGAGCAAACA[C/T]GTCCAATGTCTCACT | 8816 |
rs201631331 | snp | G/T | 1.64814e-05 | 0.00287061 | missense | DCAF5 | GRCh38.p7 | 14:69054492 | TCTCTTCTTTAAAAG[G/T]GTCCTTGCTGCAGCC | 8816 |
rs201797911 | in-del | -/TTTC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120031 | GGTCTTTTAAAAATG[-/TTTC]TTTCTTTCTTTCTTT | 8816 |
rs201827785 | snp | C/G/T | 0.00478244 | 0.0486902 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098145 | CCACCTCCTAGGACT[C/G/T]TCTTACCTTATTCAA | 8816 |
rs201834044 | snp | A/G | 0.000214516 | 0.0103543 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122189 | CCCAACCACAGTGAC[A/G]TTCCCAAGGTAGAAT | 8816 |
rs201904291 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057348 | GGGAAAGCCCTTAGG[A/T]TTTTTTTTTTTTGCA | 8816 |
rs201916735 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058552 | CATATATATATATAT[A/G]GCTAGACATGTCTCA | 8816 |
rs201955188 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068717 | AAAAAAAAAAAAAAA[-/AA]GTTTACTGCAAGGCA | 8816 |
rs201992810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074191 | CACTACTATAGACAC[A/G]TTTTGTGTAATATAC | 8816 |
rs202063074 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140961 | CAACACGGTGAAACC[C/G]CGTCTTTACTAAAAG | 8816 |
rs202162713 | in-del | -/AAAG | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154614 | ATAAATAAATTTTTA[-/AAAG]AAAGAAATCAAATTC | 8816 |
rs202206318 | in-del | -/AAT | 0.0341408 | 0.126114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081051 | TAAGAGGAAAAAATA[-/AAT]AATAAGATTTAAAAG | 8816 |
rs202225296 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053663 | TTTCTTAACACAGCA[G/T]AAGCCAATGGCCAGC | 8816 |
rs267604036 | snp | G/T | | | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091098 | GCATCTCCATTCCTG[G/T]TGAGACTCAGAAAAG | 8816 |
rs367545018 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119861 | TGCAATAAAATCTTT[A/G]GCATTTCTATGACCT | 8816 |
rs367556037 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140228 | GTCAAGATAGCGCCA[C/T]TGCACTCCAGCCTGG | 8816 |
rs367624403 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132722 | TAATGTGGGGCAGCA[C/T]AGCACAGCACAGCAT | 8816 |
rs367661585 | snp | A/G | 1.65143e-05 | 0.00287348 | missense | DCAF5 | GRCh38.p7 | 14:69054684 | AGATATAAGAGTAGC[A/G]GAGCCACTTGTAAGC | 8816 |
rs367687713 | snp | C/T | 3.32934e-05 | 0.0040799 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152872 | CAGCCCCGCAGGCGT[C/T]TCCTCTGAAAGTCCT | 8816 |
rs367697409 | snp | C/T | 3.31066e-05 | 0.00406844 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091681 | GCATTTACCTGGTCA[C/T]GATCTCCTGCAAAAC | 8816 |
rs367722348 | in-del | -/AAGA | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122030 | AAGCAAAAAAAAGAG[-/AAGA]GAGAAAAGACACACA | 8816 |
rs367764688 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108425 | AAAGGGAGAAGAGAC[A/G]CAAGCTAAGGAGCCA | 8816 |
rs367843798 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140856 | GAGCGGTAGCTCACA[C/T]CTGTAATCCCAGAAC | 8816 |
rs367889490 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099952 | AAGTTTCTGATATTT[A/G]CAGAAAAGAAGTTCA | 8816 |
rs367911106 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149527 | ACAGAAAAGTGATGT[A/C]TTATTAACTAATAGT | 8816 |
rs367932218 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130389 | GAATAGTCAAATCAG[A/G]GACAAAGTAGAATGG | 8816 |
rs368034536 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059412 | AATGTGGTGGCTAAC[A/G]CTCTTTGAGCCACTG | 8816 |
rs368190670 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109169 | ACAAGGTGAAACCCC[A/G]TATCTACTAAACATA | 8816 |
rs368370920 | snp | C/T | 3.30617e-05 | 0.00406568 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122345 | TGCCATAGCAGAACC[C/T]GGCGGTCATCTCCTC | 8816 |
rs368388515 | snp | A/C | 0.000420681 | 0.014497 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152739 | GGGTGCGGGGAGGCG[A/C]GGGGAGGGGAAGGGG | 8816 |
rs368393133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116230 | GCTCTCCTGGCTTGA[A/G]AGACACTATATATCT | 8816 |
rs368421160 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074323 | GACATTTTTCTACCA[C/T]TAGGTAACACTCATT | 8816 |
rs368425081 | in-del | -/TTAT/TTATTTAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077365 | ACCACGACATGTAGC[-/TTAT/TTATTTAT]TTATTTATTTATTTA | 8816 |
rs368441131 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129184 | TAGTAACTAACATGA[C/T]GATGACAGCCCAATC | 8816 |
rs368450329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058473 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 8816 |
rs368480473 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089440 | TTCTTTCAAGGAAAA[A/C]CACTTACCCCAGCCA | 8816 |
rs368592153 | snp | C/T | 6.59435e-05 | 0.00574172 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116404 | GAGTCCCACTCCTTC[C/T]TTTGAATTGGCTGTG | 8816 |
rs368631150 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114544 | TTACATTAAGTTCTG[A/G]AAAGATAAGAAACTG | 8816 |
rs368677504 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121277 | AAGGAGAATTAGAGA[A/G]TGGTAACAGAAATCA | 8816 |
rs368680523 | snp | A/G | 0.000153988 | 0.00877328 | missense | DCAF5 | GRCh38.p7 | 14:69055347 | CGCTGACCCCAGCGT[A/G]CAGTTGGAGGATAGT | 8816 |
rs368690063 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098034 | TGAAAACCCTCCAGC[A/G]GCTCCCCATTTCAAC | 8816 |
rs368742457 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105944 | ATATATATATATATA[-/T]ATCTCCTATTGGTTC | 8816 |
rs368897129 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088570 | ATCTGGGTCCATCTG[C/T]ATGGACTGAATAATC | 8816 |
rs368910307 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137274 | CCTCAAAACCAGTAA[A/G]GAAAGTTATTAAGTT | 8816 |
rs368926057 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061401 | AATTCTCATTTTCTC[A/T]GATGTGGAAAAAATG | 8816 |
rs368987605 | snp | C/T | 8.23974e-05 | 0.00641809 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055483 | GTTGGCGTAGTCATG[C/T]GACAGGCCACTCCCA | 8816 |
rs369071001 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084072 | AGTGGTAAAACCCCA[C/G]CTTTTCTCATCCTGC | 8816 |
rs369072262 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053161 | GAATCTATATTCTCT[C/T]GAATCTGATCTTAAG | 8816 |
rs369104749 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059699 | CTTAGTGCCATGCCA[C/T]TCCCAGCCAGACTGT | 8816 |
rs369129925 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091274 | AGATACATGTCTCTT[C/G]GATGGTACTTAGGGT | 8816 |
rs369188972 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109523 | TAACCACTATTCTGA[C/T]TTCCATAACTTGCCT | 8816 |
rs369189296 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077639 | TGCCTCAGCCTCCCA[A/G]TGTGTTGGGATTATA | 8816 |
rs369217472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135511 | ATAGTTTGCATTGTG[A/G]GCTGAACTGGCTGCT | 8816 |
rs369248320 | snp | C/T | 6.61682e-05 | 0.0057515 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116512 | TGTGGAAAGAAAAAT[C/T]ATAATCAGTTCACTC | 8816 |
rs369260220 | snp | A/G | 0.000469889 | 0.0153207 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152988 | CTTCATGCTGGAACC[A/G]CCGCCGCCGCCGCTC | 8816 |
rs369305570 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054822 | AGGAGAGGTCATCCA[C/T]TTTGATCTGGGGGTA | 8816 |
rs369391790 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096153 | CAGTCCACACTGGTC[A/G]CATTCAAGTATGTTT | 8816 |
rs369416786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062595 | CAGATAAACAGCTCT[A/G]AATGGGAGCAAAGAT | 8816 |
rs369444539 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119139 | AAAGAGATATTTGCC[G/T]CTTCATATATGAAAA | 8816 |
rs369473975 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147927 | TTCAGGGGAAATAAT[A/T]TAGCCACTCTCATTC | 8816 |
rs369529680 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070582 | ACTTGAATCCAGGTA[G/T]GATTTTAAGTCTAAT | 8816 |
rs369552685 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128268 | CTCAGCTCACTGCAG[C/T]CTCCACCTCCCAGGT | 8816 |
rs369554376 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112744 | AATTATTCATATGAT[A/G]GTCAATACTCCGATG | 8816 |
rs369613014 | in-del | -/AAAAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088341 | ACTCATCTGTGAAAG[-/AAAAG]GTTTGTATAAAATGA | 8816 |
rs369638845 | snp | C/T | 1.65198e-05 | 0.00287395 | missense | DCAF5 | GRCh38.p7 | 14:69054386 | TCTACAGAGCCGCTA[C/T]TGCCAGTGTCCTGAG | 8816 |
rs369685131 | snp | C/T | 8.23621e-05 | 0.00641672 | missense | DCAF5 | GRCh38.p7 | 14:69054956 | CAGGTAGAGGCTCGG[C/T]GTTCATTCAGCTCCT | 8816 |
rs369732275 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143610 | CAGCTGAACATTGGG[C/T]GAGGCATTCCTTAAT | 8816 |
rs369768024 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106803 | CCAGCACATTGGGAG[A/G]CTGAGATGAGTGGAT | 8816 |
rs369789649 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122860 | AACTAAGAAATCACC[C/T]GACTCTTACAGTAAT | 8816 |
rs369794976 | snp | A/G | 3.35216e-05 | 0.00409386 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118325 | CACATACACACAAGC[A/G]TAGTGCAGAGTCCCA | 8816 |
rs369813625 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069776 | CATTGTGCCTAGCAG[C/T]AGTTAGTTTTAAAAA | 8816 |
rs369830286 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072282 | CAAAGGTAGAGAAAG[A/G]GACTATTGTGCTTTT | 8816 |
rs369898066 | snp | A/G | 0.000197788 | 0.00994258 | missense | DCAF5 | GRCh38.p7 | 14:69054081 | GGGACGAGTTATCAC[A/G]GTCAGTGTCTGAGTG | 8816 |
rs369981834 | in-del | -/GT | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125920 | AAAAGAGGCTTTTAA[-/GT]GTATCTGTAGTGTTT | 8816 |
rs370022493 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151253 | AATCTACCTAGTCAA[A/C]GAGAAAACGATCTGG | 8816 |
rs370046921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080298 | GCTGATGGTTAGTGC[C/T]TAAGAGGACCACCAG | 8816 |
rs370087953 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079200 | GCTTTCCTATTTGTT[C/T]GGCTATTCATCAGGG | 8816 |
rs370180941 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066019 | AAATAAAATACCACA[C/T]ACCCAGGAAAAAGGA | 8816 |
rs370199053 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125310 | ACAGAAGCTGACTTA[A/G]CTCCAGCAAACTGGC | 8816 |
rs370208602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102964 | GTTTGTTTACACCAA[C/T]GTCACCACAAACACA | 8816 |
rs370218711 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113610 | GCCCCAAAATCTAGG[C/T]TGGGGTTTCTAGGCA | 8816 |
rs370272840 | snp | G/T | 1.65154e-05 | 0.00287358 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091689 | CTGGTCACGATCTCC[G/T]GCAAAACAGCAGCTT | 8816 |
rs370318708 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121806 | CAAACAGGAGCCATC[C/T]GTGGGTCAGGACATT | 8816 |
rs370329815 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118306 | AGAGCAAGACAGAGG[C/T]ACACACATACACACA | 8816 |
rs370349093 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | DCAF5 | GRCh38.p7 | 14:69054188 | TGTAAGCGTCCATTG[C/T]TGTGGTTGGCACAGA | 8816 |
rs370357378 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097353 | CAAAATCACCTCTAG[A/T]TGGCAATAATATGAA | 8816 |
rs370362523 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051295 | GCACATTTAATACCC[A/C]ATTTCTTCCATAATA | 8816 |
rs370407221 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071516 | CCATTAGGTATACAA[C/T]GGCAAGCCAGCTTTC | 8816 |
rs370558512 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154326 | ACCAGAGATGGCACA[A/G]GAGCAGTTGAGTAGA | 8816 |
rs370581685 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067653 | TCCAGCCCAGATATT[-/C]TTTTTTTTTTAAGAT | 8816 |
rs370586795 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF5 | GRCh38.p7 | 14:69055248 | GCCCCAGGTGGAAGG[C/T]GTTGTCGGCAGACTC | 8816 |
rs370595624 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081783 | ATGTGTGTGTTTGTG[C/G]TGCGTGCTTACACAG | 8816 |
rs370754916 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151638 | GGAGCCGCCCCCTAG[A/C]CCTCACGTAGGCCCA | 8816 |
rs370763723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115065 | TCCTGCCTTTTGTAA[C/T]ACGGATGAGGCAGAA | 8816 |
rs370763991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074560 | CCTAATTTCTTTGAC[A/G]TCCTGGGTCAACAAA | 8816 |
rs370842196 | snp | C/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154631 | AGAAAGAAATCAAAT[C/T]CCAAAAATGTGAATT | 8816 |
rs370850395 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110338 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 8816 |
rs370882307 | snp | C/T | 1.65029e-05 | 0.00287248 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122299 | TTTCAGCTGTATGGG[C/T]TTGACCCTGGAGTGG | 8816 |
rs370888554 | snp | A/G | 3.30033e-05 | 0.00406209 | missense | DCAF5 | GRCh38.p7 | 14:69054311 | ACAGGAGGAGAAGGC[A/G]GCTCCTCAGCCCGAC | 8816 |
rs370911050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056087 | AGACCCAGCACTCAG[C/T]CCTCCATGGTAGTTA | 8816 |
rs370939922 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073296 | ATGCATGTGCACAGA[C/G]AAAAGTGAGAACACA | 8816 |
rs370947236 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087735 | AGCATCAGGCATACA[A/G]TAAATGCTCAGTAAA | 8816 |
rs371053668 | snp | A/G | 0.000181436 | 0.00952287 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075302 | ATGCCAAAGGTCAAC[A/G]GAGCCAGCAATAGCA | 8816 |
rs371108471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103412 | GGAGAACATTATTAC[C/T]TGTTACTTGTATTTC | 8816 |
rs371183517 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145803 | CCTTGAGTATCTAAA[C/T]TCAGACTAAAATAAG | 8816 |
rs371238768 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079949 | GTTAGTTTCCGTTTT[A/G]CAGAGGGTGGTCACA | 8816 |
rs371263525 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068585 | TGCCCGTAATCCCAG[A/C]TACTCAGGAGGCTGA | 8816 |
rs371367284 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137704 | CACTTGTTTCTTGCC[A/G]GTACAGTAAGCCCCT | 8816 |
rs371386301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150516 | AACTGGTAAAGAACA[C/T]TTCGTGCTTTTAAAA | 8816 |
rs371394617 | snp | A/G/T | 0.00173831 | 0.0294305 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091639 | ATCAGAAAGAAAAGC[A/G/T]TAAGTGTGAGATGCA | 8816 |
rs371455777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105886 | TCACCTTTGTAATGG[C/T]ATGAGCCAATTTTCC | 8816 |
rs371515063 | snp | A/G | 4.94556e-05 | 0.00497246 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116410 | CACTCCTTCCTTTGA[A/G]TTGGCTGTGGCCAAC | 8816 |
rs371564723 | snp | C/T | 0.00059355 | 0.0172169 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055348 | GCTGACCCCAGCGTG[C/T]AGTTGGAGGATAGTA | 8816 |
rs371574933 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142162 | TTAATTAGCTGGGCA[C/T]GATGGTGCATGCCAG | 8816 |
rs371598885 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069952 | TGAGGAATAACAGTC[A/G]TTGAGTAGCTACTAA | 8816 |
rs371626361 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066082 | TTCTGTATAAACCAA[C/T]AGTCATTTCTCTGGG | 8816 |
rs371646936 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146581 | CCAGAGGAAAAAAAA[-/A]TCTATTAAAGTATCA | 8816 |
rs371663745 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099997 | TAAGCTTTAAAAGGA[A/T]GCCAATTACAAGTTA | 8816 |
rs371724309 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083581 | AAACATTCTATGAAT[A/G]TGGGCTTATCAGATG | 8816 |
rs371734739 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051068 | AAGCATAGTCACAAA[C/T]TTCACTTGCCCCAAG | 8816 |
rs371828864 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152905 | GTGAGCAGGGGGTCC[C/T]CATGCAAGCCCCGCT | 8816 |
rs371830317 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF5 | GRCh38.p7 | 14:69054845 | TGGGGGTAATCATAG[C/T]TGTCTTCTCCAATGT | 8816 |
rs371842532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130986 | GGTGAGATAATGTTT[G/T]TAAAAGCACTTAGCC | 8816 |
rs371909092 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090275 | TATTGAGAGTCTGAT[C/T]GCCTATAGAAACTGT | 8816 |
rs371994449 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109301 | GTGAGTTGAGATCGC[A/G]CCACTCTAGCCTGGG | 8816 |
rs372025373 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF5 | GRCh38.p7 | 14:69055382 | TCACTGAGGTCACTG[C/T]CTGAGTCAGAGCTCC | 8816 |
rs372036951 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112522 | TAGGCAACATAGTGA[A/G]ATCCTGTCTCTAAAA | 8816 |
rs372253791 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112835 | GTAACTTATTCAAGA[G/T]CACATGCCTATTAAG | 8816 |
rs372279704 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148553 | TACAAAAATTAGCCA[G/T]GTGTGGAGGCACGCA | 8816 |
rs372341285 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075048 | CAAAAAAAAAAAAAA[-/A]TCCAGGTGTGAAATA | 8816 |
rs372363241 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133481 | ATAAGTTAAGGTTGA[A/G]TGATTTGCCCAAGGT | 8816 |
rs372388916 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053515 | TATGAGACAATAAGC[A/G]CACACGTGCCATTGT | 8816 |
rs372398771 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144123 | ATCTCCTTGCCTTTC[C/T]ATACTACAAATCTCA | 8816 |
rs372410141 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147192 | TGCTTAAAAATACTC[C/T]TTGATGACAGTACTG | 8816 |
rs372411890 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084716 | TATGAGTTGCTGAAC[C/T]ACATTGATTTGCCCA | 8816 |
rs372413849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113077 | TTCAGGGCAGCAGTG[A/G]GACAAAAATGACTCT | 8816 |
rs372428249 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146757 | ACTCAAAAACTATTT[G/T]TTGCACTAATAAATA | 8816 |
rs372508205 | in-del | -/T | 0.0482946 | 0.147699 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113033 | TCTTTAGAGCTGACA[-/T]TTTTTTTTTCTGCCA | 8816 |
rs372512396 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128641 | AACAGAATATTGTGC[A/G]CCTGTAGTCCCAGCT | 8816 |
rs372524184 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142444 | CTTTTTACCCATTCA[C/G]TGAATGGCCATGAAA | 8816 |
rs372597637 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132836 | ACAGGTTCAACTCTC[A/G]ATGTCGCCGGCACTT | 8816 |
rs372626758 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061686 | TATTAGGATGGCAAT[C/T]AATGCAAAGTACATA | 8816 |
rs372666986 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | DCAF5 | GRCh38.p7 | 14:69055161 | ACAGACGCTGCTGGC[A/G]AGAGGCTGCATCCTC | 8816 |
rs372710662 | snp | C/T | 3.30262e-05 | 0.0040635 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054625 | CCCTTCATCTGCCTC[C/T]CCGGTCACCAAGGAG | 8816 |
rs372732001 | snp | A/G | 2.49722e-05 | 0.00353348 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091894 | AGGAGAGAACTGGAA[A/G]GCACAAGGCACAGGA | 8816 |
rs372758352 | snp | A/G | 3.72377e-05 | 0.0043148 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152754 | CGGGGAGGGGAAGGG[A/G]GTTGATTTACCTGAG | 8816 |
rs372814302 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108911 | ACCTGACTCTTCTCG[C/T]TCTCTCTTTTGTCCC | 8816 |
rs372863993 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141698 | CAGGCAGGTGACGTA[C/G]AGTTACCTAATGAAC | 8816 |
rs372949474 | in-del | -/ATATATATATATAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105915 | CCCTAATAAACTGTC[-/ATATATATATATAT]ATATATATATATATA | 8816 |
rs372957458 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103143 | CAAATTCTCAACACA[C/T]ACCAATGAGTGAAAA | 8816 |
rs372958732 | snp | C/T | | | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055504 | GCCACTCCCACTGTT[C/T]AGCACAAGGCTGATG | 8816 |
rs373132200 | in-del | C/GG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133554 | TAGGCAGGGAAGAGG[C/GG]GGGGGTACAGGCAGG | 8816 |
rs373143665 | snp | A/T | 1.64885e-05 | 0.00287123 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118167 | TTCCCGAATGTCCCA[A/T]ATGAGAACCCGGCCA | 8816 |
rs373148713 | snp | C/G/T | 3.29849e-05 | 0.00406098 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054070 | TGTCCCTGTCAGGGA[C/G/T]GAGTTATCACGGTCA | 8816 |
rs373210752 | snp | A/G | 3.29587e-05 | 0.00405934 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062423 | AGAGCAGATCATGTA[A/G]GTGTGGGGATTAAAT | 8816 |
rs373249346 | in-del | -/AAAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093649 | GCTTGGTCACAAAAA[-/AAAC]CAGCCTGTACCAACA | 8816 |
rs373297049 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136343 | CTGGTCTTGAACTCC[G/T]GGACTAGAGCAATCC | 8816 |
rs373360107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114096 | CAAGTGTTGGTGAAG[A/G]TCTGGAGACACATGC | 8816 |
rs373417601 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135265 | GCGCTAGGGCAGTGA[C/T]GGCAAATTGTACTAT | 8816 |
rs373427740 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064290 | GACAAGTAGCATTTC[C/T]GCTCATGGGTGTCCT | 8816 |
rs373480190 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106819 | CTGAGATGAGTGGAT[C/T]ACTTGAAGTCAGGAG | 8816 |
rs373490493 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108399 | TGTGTATGTGTTTTG[A/C/G]GGGGTGGTGCAAAGG | 8816 |
rs373517863 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087063 | CAGACTATCCAGTTC[A/G]AGGCAAACATGCTTG | 8816 |
rs373530366 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150757 | ATTACCTGGGCATGA[C/T]AGCACCTGCCTGTAG | 8816 |
rs373679010 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124604 | GGCCTATTTCAACTA[C/T]GAGTTCTCTGGCCTA | 8816 |
rs373682064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151639 | GAGCCGCCCCCTAGC[C/T]CTCACGTAGGCCCAT | 8816 |
rs373852000 | snp | G/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154932 | TGCTCAAGGGTGTAT[G/T]CCTGGAGCCAGTACT | 8816 |
rs373872526 | in-del | -/CG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148100 | GATGTTCATTTTCTT[-/CG]CAAAAAAAAAAAAAA | 8816 |
rs373889132 | snp | A/C | 3.29951e-05 | 0.00406159 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055303 | AGGCAATGAGGCCGA[A/C]GACTCTGAGTCAGTG | 8816 |
rs373971566 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128342 | CAGGCAAGCACCACC[A/G]CACCCAGCTAATTTT | 8816 |
rs373984712 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143605 | TGTCTCAGCTGAACA[C/T]TGGGCGAGGCATTCC | 8816 |
rs373998102 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145990 | GGAATTAAGAGAGTA[A/G]TATGCATTTGTGTGA | 8816 |
rs374001975 | snp | A/G | 1.65255e-05 | 0.00287445 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119164 | TGAAAAACAAAGTCA[A/G]TCACCTTCACACACC | 8816 |
rs374043174 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122560 | CATTCATCTCTCCCA[A/G]GAATTGAATCTTAAG | 8816 |
rs374115854 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080499 | AATTAACCAGAAAAC[G/T]GAACTTCACCTCAAG | 8816 |
rs374180829 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138410 | AGAGTGACAGTTGGC[C/T]TCCACCCTGGAAAAT | 8816 |
rs374185908 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080073 | AGAGCAGACAGAGTT[C/G/T]TGGCTATTTTAAAAT | 8816 |
rs374202800 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155278 | CCTCTGCCCTCTTAA[A/G]CACATACCCCCTTTA | 8816 |
rs374211348 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126291 | GCCTCCTGAGTAGCT[G/T]GGATTACAGACACCC | 8816 |
rs374211495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099133 | GGTCCACACCTGTAG[C/T]ATCAGCTACTTGGGA | 8816 |
rs374230324 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116088 | AGAGAGAAGGCAATA[C/T]TAAAGGGATGCTCTG | 8816 |
rs374235862 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066107 | TCTGGGCCATCTGCT[C/T]TGGTTGGCTTAGCCA | 8816 |
rs374498280 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129165 | GTTTTAAATGATGTG[A/T]CCTTAGTAACTAACA | 8816 |
rs374506011 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103684 | GTATAGCTTGTATAT[A/G]TACATCATGCATAGC | 8816 |
rs374553393 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120790 | TTGGGTATATAAAAA[G/T]AATAAGATTCTACTC | 8816 |
rs374567730 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087917 | ACAGAGGTTTCAAAC[C/T]GGTGGATCCAGAGCA | 8816 |
rs374656276 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075034 | GTGAAACTTTGTCTC[-/A]AAAAAAAAAAAAAAT | 8816 |
rs374684260 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149820 | AACATTGGGGATACA[C/G/T]AGCATTAGCCTCAGA | 8816 |
rs374714838 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118653 | TCTGATGCCTACAGG[A/G]TGGGAGAGGGGTCTC | 8816 |
rs374714987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088196 | TGTCTTGCTCCTGTC[C/T]GCAACAAGTTGTGAT | 8816 |
rs374753545 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130239 | TGGGTCGAATATTCC[C/T]GGAACTTATCATTGT | 8816 |
rs374761499 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121759 | TGGTGTGAGCACCAG[C/T]CATTCCAATTGTACC | 8816 |
rs374776494 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074786 | CACCTGTAATGCCAG[A/C]ACTTTGGGAGGCTGA | 8816 |
rs374797197 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150646 | AATCTCAGCACTTTA[C/T]GGGGTGAGGCAGGAG | 8816 |
rs374855442 | snp | C/T | 6.58903e-05 | 0.00573941 | missense | DCAF5 | GRCh38.p7 | 14:69054798 | GCTCAGGGGACGAGG[C/T]TGGGGAGGAGGAGAG | 8816 |
rs374894224 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116433 | TGGCCAACAACCTGG[A/G]CTCCACAGGGTTAAA | 8816 |
rs374913170 | snp | A/G/T | 1.89903e-05 | 0.00308136 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053830 | GTAAGGCTACTTTTG[A/G/T]AGCTTTTTGTTTTCC | 8816 |
rs375050597 | snp | C/G | 4.94784e-05 | 0.00497361 | missense | DCAF5 | GRCh38.p7 | 14:69055357 | AGCGTGCAGTTGGAG[C/G]ATAGTACTCTCACTG | 8816 |
rs375118926 | snp | C/T | 1.76188e-05 | 0.00296801 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152953 | ACTGACCTCATGCTG[C/T]CCCCCAGGCCAGCTC | 8816 |
rs375125165 | in-del | -/GA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062671 | TGCTATGGAAAGAGA[-/GA]AGATGAAACAGCTCT | 8816 |
rs375169055 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099788 | CTCTACAAAAAAAAA[-/C]ATACAAAAATTAGCC | 8816 |
rs375203333 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081848 | GGAAACATATCAATC[A/T]GTTACTATTCATTGA | 8816 |
rs375223583 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126973 | AGATAGTAGGAGAAA[A/G]CCTAGATGACACCAA | 8816 |
rs375323249 | in-del | -/TGCAGACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114914 | CCTCTCTCAAGACAC[-/TGCAGACAC]CATGAATTGCTCAAG | 8816 |
rs375397760 | snp | A/C | 1.64947e-05 | 0.00287177 | missense | DCAF5 | GRCh38.p7 | 14:69055340 | GAGCGCTCGCTGACC[A/C]CAGCGTGCAGTTGGA | 8816 |
rs375500690 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147528 | GTCAAAAGCAACCCA[C/G]GTACCAAGCAGCTGG | 8816 |
rs375501845 | snp | A/G | 6.03798e-05 | 0.0054942 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091869 | GAGGGACAGGTTTCC[A/G]CCATAGCGCAGGAGA | 8816 |
rs375667888 | snp | A/C | 0.000620137 | 0.0175978 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152737 | GAGGGTGCGGGGAGG[A/C]GCGGGGAGGGGAAGG | 8816 |
rs375668316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148254 | ATCCCCTAAATATGC[A/G]TACTACTGTAACCTC | 8816 |
rs375684158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066457 | ACTCCTTTTTAAGTT[C/T]AGTTCCTAAGTTGAG | 8816 |
rs375698001 | snp | C/T | 1.67116e-05 | 0.0028906 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122410 | GCTGACATCGCAAGG[C/T]TGACAGATGGTTTTG | 8816 |
rs375726550 | snp | C/T | 1.65048e-05 | 0.00287265 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122305 | CTGTATGGGCTTGAC[C/T]CTGGAGTGGATGGCT | 8816 |
rs375765471 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060690 | GCACACACCACCACA[C/T]CCGACTAATTTTTGT | 8816 |
rs375769199 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106008 | AGTGTGAAATACCCA[C/G]AATAGGTAAATATTA | 8816 |
rs375786352 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108917 | CTCTTCTCGTTCTCT[C/T]TTTTGTCCCTTTAAG | 8816 |
rs375839137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122766 | TCAAAGAACTTTAAA[A/G]TAATATTTCTAGCAT | 8816 |
rs375891113 | snp | C/G | 0.000447112 | 0.0149451 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116356 | ACACCTATGAATAAA[C/G]GGGGCTCACCTCTGA | 8816 |
rs375952187 | snp | A/G | 0.000107072 | 0.00731605 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152759 | AGGGGAAGGGGGTTG[A/G]TTTACCTGAGACCAG | 8816 |
rs375959426 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052073 | TCCAGGTGTTAAGTT[A/G]TACACACCCCCATGC | 8816 |
rs375971027 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114681 | GGAACTTGTTTTTTT[-/T]GTTTTTATTTTTTTC | 8816 |
rs375990691 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | DCAF5 | GRCh38.p7 | 14:69055118 | GAAAGGGCCAGGAGG[C/T]GTTTGTCTTGGTAGC | 8816 |
rs376094370 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099866 | GTGGGAGGATCAACT[A/G]AGCCACTGCACTGCA | 8816 |
rs376115284 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111144 | CCCCTGGGCTTTATT[C/T]TCCTATAATGGTATG | 8816 |
rs376136351 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142296 | GAGCATGAATAAAGT[A/G]GCAGGGCATGGGAAG | 8816 |
rs376158206 | snp | C/T | 1.66012e-05 | 0.00288103 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119279 | GTGCAAGGTGGTCCC[C/T]GTCCACATTACAATT | 8816 |
rs376193286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133833 | GCTAGAAACACTTTA[C/T]ATTAAATAGGAAGTA | 8816 |
rs376269335 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087684 | AAATCTCAAAGAGGG[C/T]ACCATCTGGCAATGT | 8816 |
rs376273369 | snp | C/G | 3.31658e-05 | 0.00407208 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118102 | TGACATCAAACTGTT[C/G]AACACAGTCCAACAG | 8816 |
rs376286040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096794 | GGCTTATTCAAAAAC[A/G]CCCTCTACCCAAAAG | 8816 |
rs376293443 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136734 | AAGATGCTAATGGCA[C/T]ACACTGGGTAGAGGC | 8816 |
rs376330092 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138223 | CTGGAATTTAGATAC[A/G]AGACTTGAATGGAAA | 8816 |
rs376335992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109205 | AGAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 8816 |
rs376381362 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | DCAF5 | GRCh38.p7 | 14:69054080 | AGGGACGAGTTATCA[C/T]GGTCAGTGTCTGAGT | 8816 |
rs376425928 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079707 | AGGCATTGTTCCAGG[A/G]AAGGGAAGGCAGAGT | 8816 |
rs376432961 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065836 | AATAGTAGTATCAAA[C/T]TGGAAGGAGACAGGA | 8816 |
rs376466441 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144162 | CTACACTACAGGTAA[C/T]GCTGGCTATTTTCCA | 8816 |
rs376466584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072726 | AATGAGTCAAGACAT[A/G]CTAAAAATAATCTTA | 8816 |
rs376485422 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103400 | ACAGTTTTAAAAGGA[A/C/G]AACATTATTACCTGT | 8816 |
rs376502523 | snp | A/C/G/T | 0.00159649 | 0.0282165 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071046 | CAAGTGATCTGCCCC[A/C/G/T]CTCAGCCTCCCAAAG | 8816 |
rs376527674 | snp | A/T | 1.75062e-05 | 0.00295852 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055638 | ATGAAAAACAAAAGC[A/T]ACAAGGAGTAACTGG | 8816 |
rs376583954 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118320 | GCACACACATACACA[A/C]AAGCATAGTGCAGAG | 8816 |
rs376662140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130141 | CCTCAGCTTTTCTGA[A/G]CAATAAAATAAGAAG | 8816 |
rs376674973 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072771 | TACATACAGAGCAAG[A/T]TGATGATCAAAGGGA | 8816 |
rs376757505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069453 | GTGAGTTTAAAAAGG[C/G]AGAAGGCCTTCTTTT | 8816 |
rs376798131 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098912 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAAA | 8816 |
rs376931043 | snp | A/G | 4.94425e-05 | 0.0049718 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054178 | GGGACGAGGGTGTAA[A/G]CGTCCATTGTTGTGG | 8816 |
rs376965558 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102589 | ATTTTGTTAAAAACA[A/C]AGACACACACACACA | 8816 |
rs376979140 | snp | A/G | 3.30376e-05 | 0.0040642 | missense | DCAF5 | GRCh38.p7 | 14:69054392 | GAGCCGCTATTGCCA[A/G]TGTCCTGAGAGGTAC | 8816 |
rs377021888 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053600 | TGCGCGGCACACTAC[A/G]CTCACGTCTCACTAG | 8816 |
rs377069336 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066014 | CCCATAAATAAAATA[C/T]CACATACCCAGGAAA | 8816 |
rs377080885 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124977 | TGACCTAATCTCCCT[C/G]TGCCTCAGTTTCATC | 8816 |
rs377124844 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101212 | TGGAGATGGATTATT[A/C]CACCTATTAAAAAGA | 8816 |
rs377166663 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102222 | CAAGTGATTCTCCTG[C/T]TTCAGCCTCCTGAGC | 8816 |
rs377210701 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139314 | AACATAGAGACCTTG[C/T]CTCTACGAAAAAATT | 8816 |
rs377216541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081017 | CTGCTTTAGTACTAA[A/G]AAAAGGCAATAACAA | 8816 |
rs377235285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132842 | TCAACTCTCAATGTC[A/G]CCGGCACTTATTAGC | 8816 |
rs377300374 | snp | C/T | 4.9958e-05 | 0.00499765 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116344 | AGGAAAGTTTTAACA[C/T]CTATGAATAAAGGGG | 8816 |
rs377321543 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075288 | CCTCAGGGCACAGCA[C/T]GCCAAAGGTCAACAG | 8816 |
rs377336142 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113384 | CAACTCTTATCCTTT[C/T]GGAGTCAAGGGTCTC | 8816 |
rs377382340 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139404 | ACTTGGGAGGCTGAG[A/G]CAGGAGGATCAATTA | 8816 |
rs377446228 | snp | A/G | 6.61923e-05 | 0.00575254 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062532 | AAAACAGAAGGAAAC[A/G]AAAATCAGATGATGA | 8816 |
rs377480459 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116608 | AATAACCACTCCAAC[A/G]GCCTGGAGCCCCAAA | 8816 |
rs377483413 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087506 | GCCTTTAGTTAAGGC[G/T]AATTGCTTCTGTTGA | 8816 |
rs377492413 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146057 | ATGACTCCAACTGTA[C/T]TTTACAAACAAATCC | 8816 |
rs377494986 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094165 | TGGCCAGCCTCACCA[C/T]CCATAGCAGCAGGGG | 8816 |
rs377495549 | snp | C/G | 0.000817923 | 0.0202063 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053850 | TTTTGTTTTCCCTTT[C/G]TATTTATCATGTTTT | 8816 |
rs377499845 | snp | A/G | 1.65419e-05 | 0.00287588 | missense | DCAF5 | GRCh38.p7 | 14:69055227 | TTGTGGTGGTGACCC[A/G]CAGGGGCCCCAGGTG | 8816 |
rs377527124 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084822 | GAACACTATTGTGTA[C/T]AGATGTGGCAGCAAG | 8816 |
rs377536056 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128646 | AATATTGTGCGCCTG[C/T]AGTCCCAGCTACTGG | 8816 |
rs377548978 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074855 | GCTGGCCAACATGGT[A/G]AAACCCTGTTTCTAC | 8816 |
rs377560799 | snp | A/G | 0.000230783 | 0.0107396 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054265 | ACAGTTGCCAGACCC[A/G]CTGTTGAGAGTGGAG | 8816 |
rs377581880 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064029 | TAGTGGATTTTTCAT[A/G]GAGAAAGAGGACAAG | 8816 |
rs377586941 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151603 | CGTCTTCACCCCCCC[A/C/T]CCCCTGAGCCAGGTT | 8816 |
rs377642895 | snp | C/G | 1.64963e-05 | 0.00287192 | missense | DCAF5 | GRCh38.p7 | 14:69055312 | GGCCGAAGACTCTGA[C/G]TCAGTGTAGCCTGAG | 8816 |
rs377673106 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080561 | TGTCTTTTCTTTTAT[C/T]TTGATGATCTAATTT | 8816 |
rs377674208 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113183 | TTGACTAATACATAG[C/G]TTAAGCCAGGAAGGA | 8816 |
rs386381677 | in-del | -/TTAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082467 | TAGAAAAAATTCTAT[-/TTAA]TAAGGAATATTCCAT | 8816 |
rs386381678 | in-del | -/AC/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099261 | TCTCAACACACACAC[-/AC/CA]ACACACACACACACA | 8816 |
rs386381679 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122874 | TGACTCTTACAGTAA[-/A]TAGGATCTAGACAGA | 8816 |
rs386778543 | in-del | AG/GTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128670 | CTACTGGGGAGGATG[AG/GTT]GCAGGAGAATCACTT | 8816 |
rs386778544 | in-del | AGAAT/GTC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128677 | GGAGGATGAGGCAGG[AGAAT/GTC]CACTTGAACCCTGGA | 8816 |
rs397702005 | in-del | -/TTAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082470 | AAAAAATTCTATTAA[-/TTAA]GGAATATTCCATAAA | 8816 |
rs397776550 | in-del | -/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136132 | TTTTTTTTTTTTTTT[-/T]GGATACAGGGTCCTA | 8816 |
rs397840790 | in-del | -/C | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053647 | TTATTTTTTTTTCCC[-/C]TTTCTTAACACAGCA | 8816 |
rs397937897 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088990 | CTGACTTCTTGTGCA[-/A]CACTTAAAAAAAACT | 8816 |
rs397961472 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057360 | GGATTTTTTTTTTTT[-/T]GCATCTTATTTGTAA | 8816 |
rs397976020 | in-del | -/CACACACACACACACA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112629 | ACACACACACACACA[-/CACACACACACACACA]AATAACACACAAGTT | 8816 |
rs398025537 | in-del | -/TG | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095565 | CAATTGAGTGGTTTT[-/TG]TGTGTGTGTGTGTGT | 8816 |
rs398025538 | in-del | -/TGTGTGTGTGTGTGTGTGTG | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102620 | AGGTCTAGGCTAATA[-/TGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 8816 |
rs398025539 | in-del | -/AA | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141351 | TAATAAAAGAAAAAG[-/AA]AAAAAAAGGTCCCAG | 8816 |
rs398038631 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150735 | CCAGGTAATTTAAAC[-/T]TTTTTTTTTTTTTGT | 8816 |
rs398043803 | in-del | -/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079087 | TGCTACCCTGCCCCC[-/C]ATACCACTGCAAACT | 8816 |
rs398043804 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131774 | TTTTTTTTTTTTTTT[-/T]AATGATTTTATCTAT | 8816 |
rs398057197 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119718 | TCAAAAAAAAAAAAA[-/AA]GTAGGGGGGAAACAA | 8816 |
rs527246052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142424 | GAACCAATGGAGCAA[A/C]CTTTCTTTTTACCCA | 8816 |
rs527259070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133629 | ACTACAGAAGTAGCT[A/C]TAGGGATAACATCTA | 8816 |
rs527294204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084211 | GCTAATGAGTCACCA[C/T]GTGCATACCTATGGG | 8816 |
rs527300070 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076203 | GAATGACTAACGAAC[C/G]GTGCAACTGCTGTGG | 8816 |
rs527360332 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125236 | GTTGAAGGGATTGTC[C/T]GCCTTAGTAGCATAA | 8816 |
rs527445061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117488 | AATCTGCACTAAAGG[C/T]CACGGTGGGTATGGC | 8816 |
rs527475105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068620 | GGAAAATAGCTTGAA[C/T]CTAGGAGACAGAAGT | 8816 |
rs527495403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108601 | AGATTTCAGCCAGGA[G/T]GATTATAAGACAGAC | 8816 |
rs527495945 | in-del | -/GCTGGAGT | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077429 | TGCTCTGTCACCCAG[-/GCTGGAGT]GCAGTGGCACAATCA | 8816 |
rs527559680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125784 | AAACATGAATAAATA[C/T]TGAAAACCTAATGGT | 8816 |
rs527614835 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060606 | GCACAATCTTGGCTC[A/T]CTACAACCTCCGCGT | 8816 |
rs527619701 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103880 | TGTATTCTTTTGAGA[C/T]TGGCTTTTTTTCAGT | 8816 |
rs527660965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124268 | CCTTTTGGCTATTGT[A/G]AATAATGTTGCTATG | 8816 |
rs527671094 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115461 | AGGCCCGTGAAATAA[A/G]TTATAACATCACTTA | 8816 |
rs527709868 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067184 | TGTGCCTAGCACATA[G/T]TAAGGTTTTTAATAA | 8816 |
rs527712519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058279 | ATCCTAGCACTTTGG[A/G]AGGCCGTGGCGGGTA | 8816 |
rs527796998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132783 | AAGACATAGGAAAAA[A/G]TAATAAGAAAAAACC | 8816 |
rs527841745 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098131 | TTATGTCTGTGACCC[C/G]ACCTCCTAGGACTCT | 8816 |
rs527841970 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053312 | TCCTCTCCAGCGCAG[C/G]CAATGGGCTGAAGGC | 8816 |
rs527882330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099078 | CAACATGGTGAAACC[A/C]AGTCTCTACTAAAAA | 8816 |
rs527882844 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094815 | TTCTCAGGATTCCCA[C/T]CCCCTGTCCCCCACA | 8816 |
rs527926900 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050869 | ACAGAAAAGAAATAA[A/G]GGAGAGGTGTCTAAG | 8816 |
rs528006527 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155144 | CATACTCAGTCCACA[C/T]ATTCAAAACCCCCTC | 8816 |
rs528119250 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153741 | CCCTTCCCCTCTCCC[A/G]GTAAATGTTTAACAC | 8816 |
rs528135841 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094888 | TAACCAGCAACACCA[-/G]GTTAATTGTGATACA | 8816 |
rs528180748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112493 | TAATTCCATCTACTC[A/G]GGAGGCTGAGGCCTA | 8816 |
rs528222171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104437 | TAATACCAATTCATG[A/G]GAAAAACCTGAGTCA | 8816 |
rs528247569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081624 | ACAACTCTCTCTCAA[C/T]AGATTTCAGGAAGGA | 8816 |
rs528254286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088789 | GGTCAAATATAAAGC[A/C]CAATATAAGGAAAAG | 8816 |
rs528329561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139911 | GAAAGGAGAAAGAAA[G/T]AGAAGGAAGGAAAGA | 8816 |
rs528332545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136020 | CTAATCTTTAAGAAA[C/T]TTCTACTTGTTTTGG | 8816 |
rs528333903 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154262 | AAGCTACTGAAATAG[G/T]CACTTGTCAGTTTTG | 8816 |
rs528349666 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111821 | TTGTAAGTGTGAAAT[A/G]TTTTTTTATCCAGTC | 8816 |
rs528378151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146264 | CTTTTTGATGTATTA[A/T]TAACAATGTCTAATG | 8816 |
rs528397576 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147042 | TACCTGCAGATAATG[A/T]GCTTTTAGACTAATT | 8816 |
rs528407949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121682 | GCAGCTCAGAAAAGA[C/G]GTCAGAACTAGAAAT | 8816 |
rs528425436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088197 | GTCTTGCTCCTGTCC[A/G]CAACAAGTTGTGATC | 8816 |
rs528444274 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109644 | CAATGTGTATATTTA[C/T]AGTTTGTTGTTTATT | 8816 |
rs528498892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145162 | AGCTGGGACTAAAGG[C/T]GCACGCCACCATACC | 8816 |
rs528502631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137056 | TTCCTTTAAATATCT[A/G]TTTTCCAAATTTCCT | 8816 |
rs528508463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079791 | AAGAGGAAAATATTA[C/T]AGACATATATAATGT | 8816 |
rs528555563 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139611 | TTGAGGCCAGGAGTT[C/G]AAGACCAGCTTGACC | 8816 |
rs528628919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094672 | ATGATAAGGATGATC[G/T]GGTTTGCCGGGAAGG | 8816 |
rs528640195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086160 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 8816 |
rs528687529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072324 | TTTATAATATTATTT[C/G]ATTTAAAAATTATAT | 8816 |
rs528750884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080421 | GGCACTGTTTCACTA[C/T]CAAAGGAAACAAACC | 8816 |
rs528760082 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137763 | GTTACCATTAGTCAA[C/T]CAGGGTCCGAAAATA | 8816 |
rs528778258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128925 | GAGTTGGAGACCAGC[C/T]TGGGCAACATAGTGA | 8816 |
rs528793083 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075630 | GGGACTACAGGCACA[C/T]GCCACCACGCCCAGC | 8816 |
rs528793703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129746 | CTAGCCCCAGCCTCT[C/G]TGGGGCACCGGAGGT | 8816 |
rs528794480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120932 | TCCTTCATAAGCAGG[G/T]TGAAAGTACATGGAG | 8816 |
rs528813981 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076860 | CCCAGAGATCTTTCA[C/T]GTAAGGCCAAGTATC | 8816 |
rs528848357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078611 | ACACATGCTACAACA[A/T]GGATCAACTCTGAGG | 8816 |
rs528909296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078091 | GTGATTTGATAAGTC[A/G]CTCCACAAACATGCT | 8816 |
rs528918264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070113 | TAAAGCCATTCCTAA[A/C]AACTCTATCACATTA | 8816 |
rs528996007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135408 | GTACACATCTAAATA[C/T]TCTGTATGACAAAAT | 8816 |
rs529010069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135987 | TTATTCGATATGGTT[C/T]TATATTCTACATTGC | 8816 |
rs529020947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110619 | GGTGGCTCACATCTG[C/T]AATCCTAGCACTTCG | 8816 |
rs529083594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093731 | GGAATGCTCTGGTAG[C/T]GCAGCTATGTGTGGA | 8816 |
rs529122906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150971 | TAACATGATTAGTTC[A/C]GTTGTCTCTAAAAGA | 8816 |
rs529141410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109421 | AAATTTATATAGGTA[A/T]ACAACCATGAAATTG | 8816 |
rs529154167 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099985 | AGGAAAATTATTTAA[A/G]CTTTAAAAGGAAGCC | 8816 |
rs529160428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062753 | CACACTCACCCACTG[C/T]AATTCCATTGTCAAT | 8816 |
rs529216482 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | DCAF5 | GRCh38.p7 | 14:69054488 | GGAGTCTCTTCTTTA[A/G]AAGTGTCCTTGCTGC | 8816 |
rs529253297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099236 | CAGCCTGGCAACAGA[A/G]TGGGACTCTGTCTCA | 8816 |
rs529276828 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119724 | AAAAAAAAAAAGTAG[G/T]GGGGAAACAACACAA | 8816 |
rs529292791 | snp | A/G | | | stop-gained | DCAF5 | GRCh38.p7 | 14:69062461 | GGTTAACAATAGATC[A/G]ATGCCCTTTCAGCAC | 8816 |
rs529297088 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052365 | ACACTAGTCAGCGTT[C/T]GGCCCTCCCTACACC | 8816 |
rs529322034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059725 | ACTGTGAATGGGGAT[A/G]ACACCTGTGAGACAG | 8816 |
rs529327299 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095694 | TCCAGGGAAAGTGAT[C/G/T]GAGCGTATCACTTCT | 8816 |
rs529357841 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051285 | TAAAAATATCTATTA[C/T]GGAAGAAATTGGGTA | 8816 |
rs529359522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060342 | TAGCTGTGTGACCTT[C/G]GACAGTTAATTTATA | 8816 |
rs529455103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117451 | AGGATAGTAAATTTA[A/G]GTACACAGCTGTGAT | 8816 |
rs529459889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077235 | TGTGACAGCGTCTTG[C/T]TGTGTTGCCCATGCT | 8816 |
rs529461843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084886 | TCAGTATGACCCTCC[A/G]GATGACCCTAAGGAA | 8816 |
rs529528307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134768 | AATATTCTGACTGAA[C/T]TGGTTAAGACAAAAT | 8816 |
rs529540624 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098596 | CAGTTTTAAAAACAC[-/T]GACTTGGCCAGGCAC | 8816 |
rs529547934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143164 | CTTCACAATTCCACC[C/T]GTCATCCTCCACTTA | 8816 |
rs529568811 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091925 | ATCAGGCATGAGATA[A/G]GCTAAACAAGAGTCT | 8816 |
rs529568846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149247 | CACAGATTAAACAAA[C/T]GACACAGCAATGATG | 8816 |
rs529611576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149753 | CAAGAACAACAAAAT[C/G]CATAAAAGTAATCTC | 8816 |
rs529620888 | in-del | -/TTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067354 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGACAGGGTCTCAC | 8816 |
rs529637712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142513 | GTGGTGACAGAAGCA[A/C]ATTTTACTTACAAGA | 8816 |
rs529697971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147172 | TAATAATAGCTATTA[G/T]TCAATGCTTAAAAAT | 8816 |
rs529713602 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154998 | TTCATGAATGTACTT[A/G]GGGAGTGGGGAGGAG | 8816 |
rs529720173 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155331 | AAAATTGTCCCATTT[A/G]CCTCAGCATAAAAAT | 8816 |
rs529729104 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153885 | AAGGGATAAAGAAGT[A/G]GGAAGAAAATTGCCA | 8816 |
rs529729141 | in-del | -/T | 0.116488 | 0.211364 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102543 | TTTATATCCTTATTC[-/T]TTTTTTTTTTTTTTA | 8816 |
rs529736620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083061 | AAACCAGACCATACC[A/T]AGCAGGCCTCACATA | 8816 |
rs529793574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097996 | GATGCTGAACCATGA[A/G]TCTAATCCTATCATT | 8816 |
rs529823391 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143635 | CTTAATTTGGTAGGC[A/G]CCGGGGAGTGCTGCA | 8816 |
rs529857384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089064 | TCATCCTCCTAATTG[G/T]ATGAATTATTTAATT | 8816 |
rs529860798 | in-del | -/AAAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086359 | CAAGACTCCGTCTAA[-/AAAC]AAACAAACAAACAAC | 8816 |
rs529882443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067834 | TAGAGATGGGGTTTC[A/G]CCATGTTAGCCAGCA | 8816 |
rs529897662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067430 | CTCACTGCAACCCCC[C/T]GCTCCCAGGCTCAAG | 8816 |
rs529932191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141766 | GAAGCCCCAGCAGAG[A/G]CAGAAGGGAATACAG | 8816 |
rs529953401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133550 | CCAGTAGGCAGGGAA[A/G]AGGCGGGGGTACAGG | 8816 |
rs529955089 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056229 | CCCTCTTGGACATAC[A/C]GGCACTAGTTACCCA | 8816 |
rs529959794 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69075381 | TTCTCCACATGTACA[A/G]GTTGAAGTCATCAGA | 8816 |
rs529976922 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052838 | ACCAATTCTGACCAA[C/T]GGTTCTGGGTTGAGT | 8816 |
rs530013929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132024 | TGTATAGACTACATT[C/T]TGTTTATCTATTCAT | 8816 |
rs530022523 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144818 | AAAAGAGAGAAACAG[C/T]ACCTGCCTGGGAGCA | 8816 |
rs530075579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074125 | AAAGGCAGATGTTTG[A/G]TAAGAATATTGTTAA | 8816 |
rs530093039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081503 | TGAATGTTTACTGAT[C/G]TAGACATTTTAAGTA | 8816 |
rs530094339 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115013 | TATAAGTAGGAGAGA[A/T]AGTAGGTTGAGAGAA | 8816 |
rs530199240 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107306 | CCCAAAGACCCTGGG[-/T]CTGAGTGAACTTGAG | 8816 |
rs530261429 | in-del | -/GCA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147367 | ACAACAACAACAGTT[-/GCA]GCAGCAGTAGCAACA | 8816 |
rs530303156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066580 | AAAAGAAAATGAGAA[C/G]AAGGTATCTCACAGA | 8816 |
rs530312254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113425 | TGGTAAAAACTTTCT[A/G]CCATCCCTAGAAAAA | 8816 |
rs530390091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057083 | GAGGTTCTGATTCAG[C/T]AAGTCATGAACAGGT | 8816 |
rs530472775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112358 | TCCATATTGGAAAAA[C/T]TTGAAAGGAATTCTG | 8816 |
rs530506251 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076313 | CAAGAATTGAAAGCA[C/T]GGACTCTAAGAGATA | 8816 |
rs530528457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064363 | CACTGGGGTGGTTAA[A/G]CAAAGAAACTTTGAT | 8816 |
rs530566886 | in-del | -/T | 0.240765 | 0.249829 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102108 | TTAGTTTACTATAAC[-/T]TTTTTTTTTTTTTTT | 8816 |
rs530603162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087433 | CTGCCAGAGTCCGCA[C/T]TATATTGCAAGACTA | 8816 |
rs530603961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120708 | GTAAATTCTACTGTA[A/G]GTACAAACCAATGAA | 8816 |
rs530613625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138479 | ATTTAATCAAAACCA[C/T]GTTCAGGGGCAATGA | 8816 |
rs530640002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080747 | TTACCCAAAATTCCT[A/G]TGTTTCATATTTTTT | 8816 |
rs530640029 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088129 | GGGCTCTCCACAATC[A/C]CCACCACTCCTTAAT | 8816 |
rs530650120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138059 | AAGCACACACTTGAG[C/T]CATCTGTGGCAGCAA | 8816 |
rs530709043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135877 | TTTCCAAATGATCGA[C/T]GTATGATGTTATAAA | 8816 |
rs530786110 | snp | A/G | 3.32276e-05 | 0.00407586 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152817 | AATGGCATTGACACA[A/G]CCGAAGTGGCCGAGG | 8816 |
rs530829663 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138728 | AGACTTCTATTAGAC[A/G]ATCATTAGTCCTTTC | 8816 |
rs530847132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144151 | TCATTGCCTTTCTAC[A/G]CTACAGGTAACGCTG | 8816 |
rs530850859 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153590 | GAGTGGGGGAAGGTG[C/T]GGGCGGGGGCTCCGG | 8816 |
rs530868450 | snp | A/C | 0.0150606 | 0.0854603 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154110 | GAAGTGGCTGCACTT[A/C]AGTAGGATGGGAGTC | 8816 |
rs530873839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150015 | AAGGGGGCTTCCTTA[G/T]CTGAAGCAAACAGGA | 8816 |
rs530878961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095593 | TTGGACTTCTTTATT[A/G]CTCTGGTGGGGTAAA | 8816 |
rs530948399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086041 | CTGTCCAATTGCACC[A/C]AAAGGTTGCTGGGAG | 8816 |
rs531070969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092729 | ATTTTTATATTCTAT[A/G]TAGCATGATAATAAG | 8816 |
rs531073569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078932 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 8816 |
rs531080674 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102402 | ATGAGCCACCGCGCC[C/T]GACCATTAGTTTACT | 8816 |
rs531106917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144520 | GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACGC | 8816 |
rs531108325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136157 | GTCCTACTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 8816 |
rs531118040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128299 | TCAACTGATTATCCT[C/G]CCTCGGCTCCATGGG | 8816 |
rs531127699 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092737 | ATTCTATATAGCATG[-/ATA]ATAAGTATTAAAGAC | 8816 |
rs531170859 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071396 | GGCTCACACTCAGGA[A/C]CACTCTCCATCTCGT | 8816 |
rs531202868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077112 | TTTCCAGTGATTAAC[A/G]TGTTTTACTTTAAGG | 8816 |
rs531244357 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136848 | CAGGTGGAGAAACCC[C/T]GCTTTAAAAGAATAT | 8816 |
rs531271252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084386 | ATCGATGAAGCTGAT[C/T]GTATCTTGGATGTTG | 8816 |
rs531297608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142450 | ACCCATTCAGTGAAT[A/G]GCCATGAAAGTGAAA | 8816 |
rs531311625 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134715 | AGTAATCAAGGCCAG[C/T]TGTATGAGAAGTCAT | 8816 |
rs531367233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068647 | AAGTTGCGGTGAGCC[A/G]AGATCATGCCATTGC | 8816 |
rs531370295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078035 | TGAAGGAATGTTGGA[C/G]GCTGGATTAGACCTG | 8816 |
rs531413686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101619 | ATACAGTCATGCATC[A/G]CTTAATGACAGGAAT | 8816 |
rs531541663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109969 | GTTGGTCCATACCCT[C/T]GTTAACACCTAATAC | 8816 |
rs531603078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069437 | AAGGAGTTATTAAAA[C/G]GTGAGTTTAAAAAGG | 8816 |
rs531618172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108008 | TCTGTGAAGCAGCTC[C/T]TGGGCACTGGGAAGG | 8816 |
rs531646099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061480 | GGACACAGGCCAGGC[G/T]AGGACCCACTTTTGC | 8816 |
rs531665386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067278 | AAAATCTTCACATAT[A/G]GGCTCCATCACCCAA | 8816 |
rs531698528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058978 | TCCATGCACAGTGAA[A/G]TTTAGCTTAAGGGGC | 8816 |
rs531771952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090290 | CGCCTATAGAAACTG[C/T]TTCTTCCCACCCAAG | 8816 |
rs531873988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115245 | AGAGCCAGGTGCCTA[C/T]GCAACAGAAGGGGCA | 8816 |
rs531893123 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051172 | ATTTTACATATCTGG[A/G]CCTGCCACTTAAAAC | 8816 |
rs531899666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105227 | CAATAGCCAGAAGAT[A/G]GGACAATCCAAACGG | 8816 |
rs531918979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099863 | GAGGTGGGAGGATCA[A/G]CTGAGCCACTGCACT | 8816 |
rs531939650 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059690 | CCTGCAATGCTTAGT[A/G]CCATGCCATTCCCAG | 8816 |
rs531955476 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070464 | AATATAAGGCAGAGG[G/T]AGGAGACATTTTATG | 8816 |
rs531970710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149162 | CAACAAGCCCCTCAG[C/G]TAGGTGCCAATATTC | 8816 |
rs532011397 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121538 | ATTGGGTGAATGGTT[A/C/G]TAACTGAGAAAGAAA | 8816 |
rs532030747 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153866 | GTACATGGGGGGAAA[G/T]AGAAAGGGATAAAGA | 8816 |
rs532065577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148704 | CATTGCCCCCACCGC[C/T]CAAAAAAAAAGTAAT | 8816 |
rs532077769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058083 | TTCTGAACATTATAA[A/G]TACTGACCGTTCCTA | 8816 |
rs532092378 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154310 | GAATTACATCCTCTG[C/G]ACCAGAGATGGCACA | 8816 |
rs532135222 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108720 | AGAACACTTGCATGA[C/G]TACTGTAAACCTATG | 8816 |
rs532155900 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105962 | CTCCTATTGGTTCTG[G/T]TCCTCTGGAGAACCC | 8816 |
rs532181987 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079080 | AATTCCTGCTACCCT[-/G]GCCCCCCATACCACT | 8816 |
rs532182677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112041 | ATGAGAATAAAGGTC[C/T]GACAATATCAGATCT | 8816 |
rs532294122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096332 | AAGGAAGACACATTG[C/T]GATCTGTGAATGAAC | 8816 |
rs532294608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147877 | CTTATGGGTTATTCT[A/G]CTAGCTCTATAAGTT | 8816 |
rs532386051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086251 | TAATTCCAGCTACTC[C/T]GGAGGCTGTGGCACG | 8816 |
rs532397913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082407 | GCTCCATTAGGCTTC[C/T]GGATCTTTCAGTTTA | 8816 |
rs532407871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089293 | CATTTCTTAGTCCCT[A/G]AGGAGTCAACAAAAA | 8816 |
rs532427945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140063 | CTGAGCTCAGGAGAT[A/C]GAGACTAGCCTGGGC | 8816 |
rs532535838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080511 | AACTGAACTTCACCT[A/C]AAGTAGTGAAATTGG | 8816 |
rs532598601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087366 | AGTAGGAAGTGAAAG[C/T]AAGAAGAACCTTTGG | 8816 |
rs532626187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145245 | CTGATCTCAAACTCC[A/G]GGGCTCAAGTGATCC | 8816 |
rs532645950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121735 | TGATGGAAGCCATCA[C/T]CAAGAGGTTGGTGTG | 8816 |
rs532745853 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065522 | ACTGATGGTGAAAAT[A/C]GGTACAGGCAGAATT | 8816 |
rs532765327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110155 | TGCTCATTTTTTAAA[C/T]TGATTTTTTGTTTTT | 8816 |
rs532769800 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137954 | CATAGTATACATAGG[A/G]TTCAGTACCATCTGC | 8816 |
rs532770731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057015 | TTCACTTTGGAGTGC[A/G]CAAGAATCACCAGAA | 8816 |
rs532783966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062776 | TTGTCAATGAAACCA[A/G]AGCCACTTAAAACAT | 8816 |
rs532792296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063318 | TTATCATTTATGAAC[C/T]TGGGATAAATTCAAA | 8816 |
rs532817941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070313 | AATCCATTACTTTCA[C/T]ACCTAACTTACTAGG | 8816 |
rs532890704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120625 | ATGCACAACCAACAG[C/T]CACTTAAATAGAAAG | 8816 |
rs532917675 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102751 | GATAATGCCTTCTTC[C/T]GGAATACCTCCTGAA | 8816 |
rs532924765 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105427 | ATGGCCAATATTAGG[C/T]GTCAACTTGACTGGA | 8816 |
rs532949198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104180 | CTACAAACTGTTTCC[C/T]AGAGTGGCTATACCA | 8816 |
rs532950999 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078623 | ACATGGATCAACTCT[A/G]AGGACATCACATCAT | 8816 |
rs532952660 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110915 | AAAAAAGTGGTGTCT[A/G]CTGTGTAAAAGTTCT | 8816 |
rs532989081 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134811 | AAGCCACGATGCAGT[C/T]TCATAATACATTGGT | 8816 |
rs533105559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103502 | CTGTGCATCCTTTAT[C/T]CAGCCTCTTCCAATG | 8816 |
rs533116036 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140078 | CGAGACTAGCCTGGG[C/T]GACGTAGAGAAATCT | 8816 |
rs533222120 | snp | A/G | 9.88435e-05 | 0.00702937 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055093 | ATTCTCCTCAGAATC[A/G]GACTCATTGGAAAGG | 8816 |
rs533236412 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052545 | TTGCACAACCCTTCA[C/T]AGATAACCGAGTGAC | 8816 |
rs533247126 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078779 | TGATGTTTAGTGGGC[-/AG]AGAGTTTCAGTTTGA | 8816 |
rs533328288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101423 | TCCATGAACAGTGCT[A/G]TAATAAGGGGAAGAT | 8816 |
rs533329069 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078151 | TGTTAAACTTTAATT[C/T]AAAAGTTTCCTAAAC | 8816 |
rs533360753 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078950 | TCACTGCAACCTCCA[C/T]CTCCAGGATTCAAGC | 8816 |
rs533420081 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098880 | CCTGGCCGACTGAGC[A/G]AGACTCTGTCTCCAA | 8816 |
rs533429451 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061244 | TGATCCTTTTGCCTC[A/C]GCCTCCCAAAGTACT | 8816 |
rs533453226 | in-del | -/CACACA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112624 | ACACACACACACACA[-/CACACA]AATAACACACAAGTT | 8816 |
rs533453602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118607 | CATACTTGATTTTCA[A/G]AAAGCAAGGGAAAGC | 8816 |
rs533499633 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098105 | TAGACAATACCCCCT[A/G]CCCTCATCCTTTATG | 8816 |
rs533514205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100154 | TGGATATCAATAGGA[A/G]GATACATTAACTAGA | 8816 |
rs533528358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136007 | TTCTACATTGCAACT[A/G]ATCTTTAAGAAACTT | 8816 |
rs533546853 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085967 | AGTCCTGGTTTTGCT[A/C]ACAATTCGATTTGCC | 8816 |
rs533548729 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127491 | GGGTTTGGAGGCAGG[C/G]GTTGAATATATGGAG | 8816 |
rs533559294 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090972 | TTTCCTCGGCTTGGT[A/G]ACCCAGATTAGCCCA | 8816 |
rs533631306 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140956 | CTGGCCAACACGGTG[A/G]AACCCCGTCTTTACT | 8816 |
rs533678802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144061 | TTATCAATGTCCTTC[C/T]TTGATTCTTTAGCAC | 8816 |
rs533708898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093385 | TCACAGACCTGAAAA[G/T]GGCCTCAAGATGCCT | 8816 |
rs533720430 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096037 | GGATGATCTATAAGG[A/G]ATATGGGATGTTTTG | 8816 |
rs533749619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075473 | GAATAAATACAATAT[G/T]TAACAATAAACATAT | 8816 |
rs533786355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067604 | CCTGCCTTGGCCCCC[A/G]GAAGTGCTGGGATTA | 8816 |
rs533802683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059301 | TGTTGTCCCTGACAA[C/T]AGGGACTCTTCTCCT | 8816 |
rs533837618 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69089006 | CACTTAAAAAAAACT[A/G]TAAGTTCAGTAGATT | 8816 |
rs533858292 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137431 | CCATTCTATGAGCAA[-/T]TTCTGATTATTCTTT | 8816 |
rs533889605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123918 | TTGGCCAGGCTGGTC[C/T]CAAACTCCTGACCTC | 8816 |
rs533915657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074761 | GGTGTGGGCTGGGTG[C/T]GGTGGCTCACACCTG | 8816 |
rs533918410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083580 | AAAACATTCTATGAA[A/T]GTGGGCTTATCAGAT | 8816 |
rs533932948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057429 | GTAAAATGTCATTAA[C/G]CATGTTCTCTAATAT | 8816 |
rs533949087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098871 | GCACTCCAGCCTGGC[C/T]GACTGAGCGAGACTC | 8816 |
rs533990072 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053047 | AGGATCTAGCACCTA[A/G]CTGGTTAAAGTCTGT | 8816 |
rs534013141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122620 | TGATATTGAGACTCC[G/T]AAAGCCACCCTGTTC | 8816 |
rs534021894 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051763 | TCAGAAGAGGCTAAG[C/T]ACTTATTAAAATAAA | 8816 |
rs534058042 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063532 | ATCCCCTCTTAGTCC[C/G]TACCAGGAGCATGGC | 8816 |
rs534071865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113520 | CAAATTCCTTAAAAT[C/T]TCTCCCTACACTTGA | 8816 |
rs534076557 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050423 | CCTGACAAGCCTTGG[C/T]TGGCAAGAATTTTTC | 8816 |
rs534132842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082650 | TTAACCATTAGCCCC[C/T]CTCCATGGGCTTCAG | 8816 |
rs534134561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116699 | CAAGGTAAACACATT[C/T]AACCACATTTTAAGC | 8816 |
rs534149232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140192 | GAATCTCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 8816 |
rs534187145 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080653 | GAGCAAAATGCTTCT[A/G]GCCTAGATAACAGAA | 8816 |
rs534227571 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110493 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTTGTGAT | 8816 |
rs534243635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147302 | GTGCAGTATATGTTA[A/G]ATGTTGAAGGTATCA | 8816 |
rs534323320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080061 | GAGTATTCCAGGAGA[A/G]CAGACAGAGTTCTGG | 8816 |
rs534376277 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087807 | CATGAAGTTAGGAAG[C/G]CTTCAGCAGGAAGCA | 8816 |
rs534434650 | snp | C/T | 1.88493e-05 | 0.0030699 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152969 | CCCCCAGGCCAGCTC[C/T]CCTCTTCATGCTGGA | 8816 |
rs534461043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146654 | AAATGAGAACTGAAC[A/C]CTCCTAAAACACCAG | 8816 |
rs534508517 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101377 | ATCTTAGGCACTGTG[C/T]CACACACATGGATTC | 8816 |
rs534509704 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145287 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 8816 |
rs534535019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088412 | GGTGGCAATGAGCAT[A/G]AGGGAGACACAAAGG | 8816 |
rs534576436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086919 | CTCAGTGCTCAGGTA[C/T]GCCAGTGCTCAGCCT | 8816 |
rs534638799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080818 | ATTTAATACACTACT[A/G]TGAAAAAAACTAAAA | 8816 |
rs534668660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152009 | CCGGGCTCCCGCCAA[C/G]AAGTCTCCCGGGGGT | 8816 |
rs534673042 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119498 | GATGATGTAAAAAAA[A/T]AAAACAACTGTGGCT | 8816 |
rs534726036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062064 | TCTTTCTTCTTTTTT[A/T]AAAATTTATTTATTT | 8816 |
rs534743640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095090 | ATTCCTCTTCAGATC[A/G]GAGTTATACTCCTGT | 8816 |
rs534779259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121948 | GTCTGTGTGTGTTTC[C/T]GTGTACCAGACTGCA | 8816 |
rs534793353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118690 | ATCTGGCATGGTGAT[A/G]AAGAGCATGGCTCTG | 8816 |
rs534795325 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107014 | ACCACTGCATTCCAG[A/C]CTGGGTAACAGAGCA | 8816 |
rs534797267 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074392 | TAAGAAACAAACCAT[A/C]CTAAGAAAAAGAAAA | 8816 |
rs534809016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127789 | TTTCTCTTAATTTTG[C/T]TGTGAACCTGAAACT | 8816 |
rs534815442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136264 | GAGACTACAGGTGCA[C/T]ATCACCATGCCTGGC | 8816 |
rs534852855 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062762 | CCACTGCAATTCCAT[C/T]GTCAATGAAACCAAA | 8816 |
rs535069341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135170 | TTCGCAATAACACTA[C/T]AATGTTATTTGCCTT | 8816 |
rs535069746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097305 | ACAGCTTGTTTCATA[C/G]AGGAGCCACTCATTG | 8816 |
rs535089574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063858 | AGCCAGCTTTAGGTG[C/T]TCAATCTATTTGATG | 8816 |
rs535091426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075567 | GCTCACTGCAACCTC[C/T]GACTCCTGGGCTCAA | 8816 |
rs535102967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130061 | TTTCCCAAAGGGTCC[C/T]GAGCTATAAGCAGAA | 8816 |
rs535157254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059998 | TGACTAAACAATAAA[C/T]AGGGAGATTTATCAC | 8816 |
rs535168176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078291 | ACACAAAAAGATGTT[A/C]AACATCACTGATCAT | 8816 |
rs535176252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116890 | ATCCAATTGTATTAG[A/T]TTTAGAAAAGTTTTT | 8816 |
rs535176870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103236 | GAAATAATGCCATAT[A/G]TTTTTCTACGGGTAC | 8816 |
rs535185796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117812 | ATGCAGGAAAGTGCA[C/T]AACGCCCCCATTCTC | 8816 |
rs535296833 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145691 | AACAATGTGAGGCAA[C/T]AAAAATTGAAAACAG | 8816 |
rs535343602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149414 | TGCTGTCATAATTTC[A/T]CTTCCAAGCACAGCA | 8816 |
rs535372693 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125992 | AGATATAAGGTTAAT[A/G]TACAAAAGTCCATCA | 8816 |
rs535376122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142939 | TATACCTACTCCTAA[G/T]CAGACTAAAGTAGGG | 8816 |
rs535409813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092220 | ACCAAAAGCATACTC[A/G]TCAAGACCCTGAGAA | 8816 |
rs535412049 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086339 | CTCCGGCCTGGGTGA[C/T]AGAGCAAGACTCCGT | 8816 |
rs535419110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060731 | GAGACAGGGTTTCAC[C/G]ATTTGGGCCAGGCTG | 8816 |
rs535431615 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052071 | AGTCCAGGTGTTAAG[C/T]TGTACACACCCCCAT | 8816 |
rs535449337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089822 | ATATTACCGGCTTCT[A/G]GTAGGAAGAGGCTAG | 8816 |
rs535461773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083469 | ACTGCGGCAGTGGAA[C/T]CTAAAGTTGCAGGGG | 8816 |
rs535530182 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050614 | CTTCACTGCATTGTT[C/T]CCTCTGTTCCAACTA | 8816 |
rs535604885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098612 | GACTTGGCCAGGCAC[A/G]GCGGCTCACGCCTGT | 8816 |
rs535608768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084666 | AAAAGAAGCTTATGG[C/T]CTTCTTTTCATCTTG | 8816 |
rs535628559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065652 | TGATATTATTGAATA[C/T]AGCTGCTACTGAACA | 8816 |
rs535647024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085193 | TGTTTAATAACTTAA[A/G]TTTGCCTCAAGTTGC | 8816 |
rs535672254 | in-del | -/G | 0.0577344 | 0.159793 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150243 | AGCTAGAGGGAGTAT[-/G]GGGGGGAAGGAAAAG | 8816 |
rs535683519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068199 | GGAAGCTCTCTGAAG[A/G]CAAAAAATGTTCATT | 8816 |
rs535757055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150065 | GCTGTGTACTCATAA[C/T]GGAAGGTAAATAGCT | 8816 |
rs535768957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101769 | CAAACCTGTACAGCA[C/T]GTTACTATATGTTAT | 8816 |
rs535788971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083917 | GAGGATACTTCATTT[G/T]CTTCTTATGTAATCT | 8816 |
rs535789408 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079414 | CTCTTCCTCTTGGAA[C/T]TCTTCTTCCACCCAC | 8816 |
rs535847786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090570 | AACAGGCATTTATTC[A/G]GCTCCTATTACATCT | 8816 |
rs535856101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098043 | TCCAGCGGCTCCCCA[C/T]TTCAACTAGAGTAAA | 8816 |
rs535860304 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125095 | TCACACAATAAAGTC[A/C]TTGAGCTAAGATTCA | 8816 |
rs535896922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148719 | CCAAAAAAAAAGTAA[C/T]GTTCACTCAAAATCA | 8816 |
rs535898951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141117 | CCAGCCTGGGCCACA[G/T]AGCGAGACTCCATCT | 8816 |
rs535905546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139359 | CGTGGTGATGCACAC[A/C]TAGGTGTACATCACC | 8816 |
rs535933690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097699 | TCAAGCAACTCTCCT[C/G]CCTCAGCCTCCCCAG | 8816 |
rs535943651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107402 | AATCACCTTGGGTAT[G/T]TGCTAAATAATGGCA | 8816 |
rs535966911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140097 | GTAGAGAAATCTCGT[C/T]TCTACTAAAACTACA | 8816 |
rs536079157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059210 | CCACCTCAGCCTCCC[A/G]AGTAACTGAGAGCAC | 8816 |
rs536097285 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108535 | CACTAACACAGAGCA[A/C]AGATGTTTATGGCAG | 8816 |
rs536105150 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058284 | AGCACTTTGGGAGGC[C/T]GTGGCGGGTAGATCA | 8816 |
rs536199331 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088739 | CAGAACACAGAGCCT[C/T]AGGCTGTGGGTGTTC | 8816 |
rs536232346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082569 | ATAACAAAGTGGCCA[C/G]CGTTACTTAAAGATG | 8816 |
rs536279647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122955 | TTGTTATTGTTTTTT[C/T]CCATTTTTACTTTTT | 8816 |
rs536310587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072578 | GATTGTGCCTGTGAA[C/T]AGCCACTGCACTCTA | 8816 |
rs536370323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131270 | TCTTTTCTTTTTTTT[A/T]AACTGTGAAGCCTAA | 8816 |
rs536389572 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080270 | GCTGGTTGGGGCCAC[G/T]GAGTGGGGCGCTGCT | 8816 |
rs536393965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081845 | GAAGGAAACATATCA[A/G]TCAGTTACTATTCAT | 8816 |
rs536424508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115487 | ACTTAGTTTCCATGA[C/T]ATTCTTCTGCAACAC | 8816 |
rs536431730 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145919 | GCTCTTATAAACTTA[G/T]GCTCTCTTTGCCTTG | 8816 |
rs536487456 | in-del | -/ACAAAAAAA | 0.358303 | 0.225323 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099777 | TGAAACCCTGTCTCT[-/ACAAAAAAA]ACAAAAAAAAAATAC | 8816 |
rs536489446 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154510 | TACTAATAACAAATA[C/T]GCAAATGTTTCATAT | 8816 |
rs536559721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114499 | TGTCTCAATTTTTTT[A/G]AAGGATGCATATGCA | 8816 |
rs536560624 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140674 | AGTATAATAAGAACT[A/G]TAAGATGATGTATAT | 8816 |
rs536631795 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077111 | ATTTCCAGTGATTAA[C/T]GTGTTTTACTTTAAG | 8816 |
rs536680510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056414 | CTAAAAGGCAGCAGA[A/G]CTAGGATTCAAACTC | 8816 |
rs536706111 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123768 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 8816 |
rs536706622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063804 | ACATATCTTTTTTAT[A/G]ACAGCAAAAGGTTCC | 8816 |
rs536721036 | snp | C/T | 1.6489e-05 | 0.00287128 | missense | DCAF5 | GRCh38.p7 | 14:69054590 | GGGGCTGGGTTGTCT[C/T]TGTGGCTGGTTCCTG | 8816 |
rs536740264 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102039 | TATATAAATATTACA[A/C]ACAGGCTACGCTACA | 8816 |
rs536769546 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104199 | GTGGCTATACCATTA[C/T]ATATTCCCACCAGCA | 8816 |
rs536810973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087725 | TATCTATCACAGCAT[C/T]AGGCATACAGTAAAT | 8816 |
rs536842184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088297 | AACTTGTATGTGTTG[C/T]GACTTGTGACCTCTC | 8816 |
rs536923345 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153157 | GGCTTCCTGACGGTC[C/T]CCTCCCTCTCCTTCC | 8816 |
rs536943855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104730 | AGTGTAGCAGCGGGC[A/G]CCTGTAATCCCAGCT | 8816 |
rs537035958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077670 | GGAATAGGCTACACG[A/C]CTAGCCAGGTCTAGA | 8816 |
rs537072909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069069 | AACTACTTGCAACCA[A/G]TTAAAAACAGCTGTT | 8816 |
rs537090142 | in-del | -/A | 0.383439 | 0.21141 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068699 | ATGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8816 |
rs537092277 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151827 | GCCTGTCGCTAGGAG[C/G]CCCGGGAGAGCGAGG | 8816 |
rs537144022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110307 | ACAGAGTCTCACTCC[A/G]TCACCAGGCTAGAGT | 8816 |
rs537229377 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066337 | AGATGGGGTTTCACC[A/G]TGTTGGTTAGGCTGG | 8816 |
rs537235271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079932 | GTGCTGGGGGTTGGG[A/G]TGTTAGTTTCCGTTT | 8816 |
rs537241647 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146543 | ACAGGCAAGAGCATT[C/T]TTGCTGTATTAAGTA | 8816 |
rs537282346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062881 | TGAACTGCTTGGGAA[C/T]AGTTAGGCAGCTGGA | 8816 |
rs537283474 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129394 | CGTTGGCAGAAAAAC[A/C]ACCAGTACAAATTGA | 8816 |
rs537305050 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144911 | GTCTAGATCTCAGCT[C/T]CCTTTCCTGTAAAAT | 8816 |
rs537371467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137313 | ATGCATTGCCAGGTA[A/C]TTCCAGATCACAAAT | 8816 |
rs537383407 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119831 | TTCAGCAGAACACTC[A/C]CTAATCATGAGACCT | 8816 |
rs537396121 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070775 | GTTCTATTCCTTCCT[C/T]TAATTTTTATTTTTC | 8816 |
rs537413938 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085265 | TCAACAGCAATGAAG[A/G]CAAGCAGAAAAAGCG | 8816 |
rs537425173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085149 | TACATACAAACCTAC[A/G]ATTCCCATTCTCTGA | 8816 |
rs537476132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078220 | ATGGGCCAAGGACTT[A/G]AACAGACATTTCTCC | 8816 |
rs537476436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126999 | ACCAAATGCTGGTCA[C/T]GATGTGGAACAACAC | 8816 |
rs537486185 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135552 | ATAACATTTTTACTT[C/G]AAATTACTGAAAAAG | 8816 |
rs537542399 | snp | C/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124914 | TGTCTCTAGCAAAAG[C/T]AAAAAGTTAAAAGAG | 8816 |
rs537552716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125825 | AGTTTCGAAAGGATA[C/T]GAAAGGGATAATATC | 8816 |
rs537554582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116184 | CTCAGCAAGGAGTAC[A/G]GATTTGTCGCTGTCT | 8816 |
rs537571679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143443 | TAATACTACCCTAAC[A/T]TACAAAACATTCTTT | 8816 |
rs537588574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084547 | TGTTGGTGTTGATGA[C/T]GATAAAGCTAATGCA | 8816 |
rs537611272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120101 | TTTTCTTCTTTCTTT[C/T]GAGACAGGATCCTGC | 8816 |
rs537695831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149372 | TTAAAGTATCTTAAC[A/G]TGTCAAATAACCATT | 8816 |
rs537719969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122130 | GCTCAATGAAATACA[A/G]GAAGAAAAATAAGGA | 8816 |
rs537734116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127514 | ATATGGAGCAGAGAA[A/G]ATTTTTAGGGCAGTA | 8816 |
rs537748216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119353 | TGCTAATACAAATTA[C/G]AAGTGTTAACTGGAA | 8816 |
rs537754905 | in-del | -/TTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114675 | TGGAGATGGAACTTG[-/TTTT]TTTGTTTTTATTTTT | 8816 |
rs537759340 | snp | G/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154337 | CACAGGAGCAGTTGA[G/T]TAGAATCATCATTGA | 8816 |
rs537820625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097495 | ACCTACTATATGCAA[C/T]GTACTTTCTATTCTA | 8816 |
rs537839097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059335 | CAGGAAGGTGGCAGT[A/G]AAGGACAAGGACAGA | 8816 |
rs537856505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089211 | ACTCAAGATTTACTT[C/T]AACAAATTTTTATTG | 8816 |
rs537873975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059916 | ACAGATAAAACACTT[C/T]TTTCTCTTTTTCCTC | 8816 |
rs537903194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076306 | ATATATCCAAGAATT[G/T]AAAGCACGGACTCTA | 8816 |
rs537950314 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093155 | TTACAGAGGGATGAC[G/T]GCTCATAGTCCATGT | 8816 |
rs537987438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106471 | CCTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTCA | 8816 |
rs538036605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083316 | TCAAAAAGAGTTATA[A/C]ATGGCTGATTTAATA | 8816 |
rs538046844 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113671 | AACTCAGCATAACTA[A/G]TCCTACATGGAAAAG | 8816 |
rs538047145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092077 | ACAAGTTACTTCAAT[G/T]GTCAGTTCTCTTGCT | 8816 |
rs538088600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133151 | TTTTAACAACCCCAC[A/G]AAGTAGGAATTCACA | 8816 |
rs538117697 | snp | C/T | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050654 | TCAGTTCCAGAGTCT[C/T]GCTATCTTAAGTCCC | 8816 |
rs538150914 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052575 | CTGCAACGCTGAAAA[G/T]CTGTTGCTCTTTTCT | 8816 |
rs538172093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108762 | TGGGTGAGTAGAAGA[C/T]AGAAAGAAGGGAGTA | 8816 |
rs538191872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089691 | ACCTGCCCCAATGCA[A/T]CTGAGCAAAATGGGT | 8816 |
rs538228080 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154465 | AATTATTTACTTCTA[C/T]TTTTTGTTCAGTGAC | 8816 |
rs538280132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081746 | ATCCATTGACCTTTA[C/T]AGAAAATGTGTGTGT | 8816 |
rs538291274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147507 | ACAAGAGAGGATAAG[C/T]GACCTGTCAAAAGCA | 8816 |
rs538331892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105514 | GTTTCCAGAGGAGAC[C/T]GAGATGTGAGTCAGT | 8816 |
rs538441160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066032 | CATACCCAGGAAAAA[A/G]GATCTCATTCCTGAG | 8816 |
rs538477395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066917 | AATGAGTACGTTTTT[C/G]ACTCAAAAGCTGAAA | 8816 |
rs538535825 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116901 | TTAGTTTTAGAAAAG[G/T]TTTTAAACCATGCAC | 8816 |
rs538619956 | in-del | -/T/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110270 | CATCTTTTCACTTAC[-/T/TT]TTTTTTTTTTTTTTT | 8816 |
rs538624579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088243 | AGGGGTCTCTATTGA[A/G]AGCCCAAAAATCTGG | 8816 |
rs538667539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130230 | CTGAAATTCTGGGTC[A/G]AATATTCCTGGAACT | 8816 |
rs538678025 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136541 | CTTCTCGCTATTTTT[G/T]TTTAATTTTGGAAAA | 8816 |
rs538680034 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145776 | TTTAACTTTAAAAGA[A/C/G]TTTCATTCCACCCTT | 8816 |
rs538726201 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076510 | ATAAACCGTGACGTT[A/G]TACTAAATGAAATAA | 8816 |
rs538742655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138403 | CTCAACCAGAGTGAC[A/G]GTTGGCCTCCACCCT | 8816 |
rs538753431 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143951 | ACTGCATTCAGACCC[A/G]CCATATTTCACTTCA | 8816 |
rs538760213 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120253 | TATGCCTGGCTAATT[A/T]AAAAAAAAATTTTTT | 8816 |
rs538762250 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108208 | TTCATTCAACATACA[C/G]TCTGTGCCAAAATAG | 8816 |
rs538775346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087658 | CAGATTGTATAAAGG[A/G]CTTTGAGTGCAAATC | 8816 |
rs538861184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057574 | GTATTACTACCCAGC[A/T]CCTACATTTTCCCTT | 8816 |
rs538886137 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153050 | GGCCGCTGCTCCCCC[C/G]ACCCGGCCCTCCCCC | 8816 |
rs538925791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131158 | ACATACACAAATTTA[A/T]ACATACAAAGACAGA | 8816 |
rs539019456 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101911 | GTACACCTGTATAGG[G/T]TATCCACCATGAATA | 8816 |
rs539023918 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070430 | TCAGAAAGCTTCCAA[A/G]ATTATTAAATCAACA | 8816 |
rs539026421 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116999 | TTCTCTTCTGGTTCA[C/T]AATGCTCCCTAACAT | 8816 |
rs539029282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063021 | AAAACCCCATAAAAA[A/C]CAAAACCACTGGGGG | 8816 |
rs539056454 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103011 | CTACATTATGACAGC[C/G/T]ACATTACCAGGTGAC | 8816 |
rs539058400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092922 | TACTATGTTCTGGTT[C/T]ACCTAATATTCTTCT | 8816 |
rs539067981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063702 | CTTCCCCAGAAATAA[C/T]ATGGCTCTAGGGGTA | 8816 |
rs539278685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136499 | TGACAGATACACACA[A/G]ATTTGAGAAAATGTA | 8816 |
rs539298148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111749 | GGTTACCTGTGAAAA[C/G]AGCAGAAATCATCTA | 8816 |
rs539313346 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067428 | AGCTCACTGCAACCC[C/G]CCGCTCCCAGGCTCA | 8816 |
rs539316232 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099929 | GAATAAAATAACATT[-/A]AAAAAAAAAGTTTCT | 8816 |
rs539412134 | snp | A/G | 3.93074e-05 | 0.00443308 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053829 | TGTAAGGCTACTTTT[A/G]TAGCTTTTTGTTTTC | 8816 |
rs539435477 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084046 | ATCTTCTTGCAGCTA[A/C]AAAAACCGTCAGTGG | 8816 |
rs539468924 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076481 | ATGAAATTCTGACAC[A/T]TGCTACAACATGGAT | 8816 |
rs539475691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061811 | TTGCAGCATACAAGG[C/T]AGTGTCTAGAAGACA | 8816 |
rs539498352 | snp | C/T | 3.30469e-05 | 0.00406477 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69119217 | ATCATGGAGGATAAC[C/T]TGCTCATCATTGCCT | 8816 |
rs539500828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148817 | AGGGCAATCTGTTAT[C/T]CTCATTTTACAGATG | 8816 |
rs539554337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109511 | CTTACCCAGAGGTAA[A/C]CACTATTCTGACTTC | 8816 |
rs539595109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090825 | ACACTAAACATTAGC[A/G]AGAGACTAAGGTTTT | 8816 |
rs539608554 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128384 | AGAGACAGGATTTCA[C/T]CATGTTGCCCAGGCT | 8816 |
rs539622199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092645 | AATAGAAACTTGTTT[A/G]TAATCGATAATTTGT | 8816 |
rs539623650 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068864 | CAAGGATACTGACAA[C/T]ACGGACAGAGCAGTG | 8816 |
rs539640395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079170 | GGTTTTACTATTTCA[C/T]CGTGAAGCATCAGTG | 8816 |
rs539661152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069581 | TGGGACTACAGGCAT[A/C]TGCCACCATGCCCAG | 8816 |
rs539703273 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064042 | ATGGAGAAAGAGGAC[A/G]AGGAAAAGTTAGGCA | 8816 |
rs539734877 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144303 | CAAGGCCAGGCGCGG[A/T]GGCTCACGCCTGTAA | 8816 |
rs539851738 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142653 | CTAGCACTCTCTGAG[C/G]AAATCAGCCCATATT | 8816 |
rs539871123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134095 | GAGTTCATCTTCTAA[C/T]ATCCCCATTTTGCCA | 8816 |
rs539935660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149320 | ACAGCGATGCCCCTT[G/T]CTGGTCATAAACAAG | 8816 |
rs539955643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113918 | CCTTCTTTTATTCCA[A/G]AAAGAAATTAGTCAT | 8816 |
rs540000421 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069082 | AATTAAAAACAGCTG[-/T]TTTTTTCCAGTTACA | 8816 |
rs540004168 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144465 | TAGTCCCAACTACTC[A/G]GGAGGCTGAGGCAGG | 8816 |
rs540028733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089271 | CAAGACAATGATGAA[C/T]TAGCTACATTTCTTA | 8816 |
rs540030708 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147754 | TAATACTTTGAAACA[A/T]CATAGTTGCTCATGC | 8816 |
rs540175517 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111991 | TGGTGGGACCCTTAA[A/C]TAACATCATAAAGGT | 8816 |
rs540239166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095884 | GCTCTATAAGACCGG[C/T]GGAATGCTTGGGGTC | 8816 |
rs540241203 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153378 | GCTTTCCCAGTTGAG[A/C]CGCTTCCCGCCTGGG | 8816 |
rs540272307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137869 | TACTTTATTACTATT[A/G]TTGTTAATGTATTAC | 8816 |
rs540279588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087858 | ATGAGTTAGTGACAG[A/C]CCATGGCACTAAACA | 8816 |
rs540290312 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093903 | CAGAGAAATGCCCTT[A/G]TAATGGTCCTAAACA | 8816 |
rs540328730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104105 | CATCTCTCCTAGATA[G/T]AGATCCAAGAATGAA | 8816 |
rs540452326 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131532 | AGGAATTCAATCACT[C/T]ACATATCTCATTTTA | 8816 |
rs540474435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140630 | AACCCATAGGAAGAC[C/T]GTAAAAACAAAAAAA | 8816 |
rs540481180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138555 | AACACTTTACTTGAG[A/C]AAGTCCTTTTTAAAT | 8816 |
rs540591265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079549 | CTGCAGAATTCATTA[C/T]GGCATTTCACGGTTG | 8816 |
rs540591405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070185 | GCTCTGGAAAAGCAA[C/T]TCAACCTGTGAAAAC | 8816 |
rs540592662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087262 | CCCTATTAAGAGACT[C/T]GCTCACTGAGTATGT | 8816 |
rs540641131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080440 | AGGAAACAAACCCAA[A/G]GTACTTCATCGTATT | 8816 |
rs540685114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152589 | ATAGAAGACATCCTC[A/T]CCTTCCCCTCCCCCT | 8816 |
rs540750391 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067706 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTT | 8816 |
rs540754704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078613 | ACATGCTACAACATG[A/G]ATCAACTCTGAGGAC | 8816 |
rs540784380 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128116 | TAGAGGGATAGATGA[C/T]TAATATGGACAATTG | 8816 |
rs540795753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081988 | AAAAACCAGATGGCT[C/T]GCTAGCCTGGATCAG | 8816 |
rs540810782 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108443 | AGCTAAGGAGCCAGT[A/G]CAGTCAGAACCTTAT | 8816 |
rs540814144 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073040 | GAAACACTGCATAGT[G/T]CATTTTAGAATAAAG | 8816 |
rs540843155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065419 | CTTCTTGGTAGCAAT[C/T]TTAACACAAGGTCTT | 8816 |
rs540884800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055715 | TCCCCAGACTCTCCC[C/T]GTAATTTAACTAGGA | 8816 |
rs540950591 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110701 | GGTAACACAAAGAGA[C/T]GCTTTCTCTAACAGA | 8816 |
rs540972217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134920 | AAATATTCACACCCA[C/T]TGACTCAGAATTCCA | 8816 |
rs541082267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144348 | GAGGCCGAGGTGGGC[A/G]GATCACAAGGTCGGG | 8816 |
rs541099480 | in-del | -/A | 0.0614824 | 0.164198 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058877 | GTAAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8816 |
rs541154651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117466 | GGTACACAGCTGTGA[C/T]CATTACAATCTGCAC | 8816 |
rs541279784 | snp | A/G | 9.88875e-05 | 0.00703093 | missense | DCAF5 | GRCh38.p7 | 14:69054161 | TTATTGTGAGGGTGA[A/G]GGGGACGAGGGTGTA | 8816 |
rs541359860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063178 | GCCTTAAAGATACCA[A/T]GTATAGATTAAAGTC | 8816 |
rs541395491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092529 | AGGCTGAGGAGGGAG[C/T]GCCACTTGAGCCTAG | 8816 |
rs541426513 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098658 | GGAGGCCGAGACAGG[C/T]GGATCACGAGGTCAG | 8816 |
rs541440387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148538 | CGTTTCTACTAAAAA[A/T]ACAAAAATTAGCCAG | 8816 |
rs541500561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107857 | CTATATATTCATTCA[A/G]TATTTACTAAGTTTC | 8816 |
rs541503186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127158 | CCAAAGGAGTTGAAA[C/T]TTGTATCTACACAAA | 8816 |
rs541557509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069146 | ACTGAGAGTGAATAC[A/G]TGTCTAGAAAAAGAA | 8816 |
rs541565772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093288 | CACATCAGAACTCAC[G/T]CTGTCTCATGCAGAC | 8816 |
rs541622493 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113899 | GTCCCCATGGCACTA[C/T]GCTCCTTCTTTTATT | 8816 |
rs541665434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068445 | GGCTCATGCCTGTAA[C/T]CCCAGCACTTTGGGA | 8816 |
rs541673818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142343 | GACAAACTACTACTG[C/T]CAAGTCTTTCCCTAA | 8816 |
rs541683089 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126442 | CATTACAAGCTTGAG[A/C]CACCATGCCTGGTCA | 8816 |
rs541690722 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096418 | AGATGAATTCAGTAT[A/C]CTTTTTGAATCTCCA | 8816 |
rs541736691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134470 | GCTCAAACTTCTGAA[A/T]TTTGGAGAACAGGCA | 8816 |
rs541759723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099707 | CAACACTTTGGGAGG[C/T]CCAAGCAAGAGAATT | 8816 |
rs541759972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102169 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGTTCAC | 8816 |
rs541811681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147905 | GTTCCAATGCCTTAA[A/G]CTTCGATTCAGGGGA | 8816 |
rs541851537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149008 | GGTCTATTAACAATA[A/C]TGTAATAACAAATGT | 8816 |
rs541858700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075053 | AAAAAAAAAAATCCA[A/G]GTGTGAAATAGGAGG | 8816 |
rs541899026 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050785 | TTGTCATGGATGTGG[A/T]ACACTGCAGTTTTTC | 8816 |
rs541905976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132765 | GCTTAGTCTCCACGT[A/G]GTAAGACATAGGAAA | 8816 |
rs541910198 | snp | C/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088743 | ACACAGAGCCTCAGG[C/T]TGTGGGTGTTCTCAG | 8816 |
rs542052284 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077820 | AATCAATTTCCTAGC[C/T]TTCAAAACACTTGTA | 8816 |
rs542055302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116238 | GGCTTGAGAGACACT[A/G]TATATCTTAAGAAAT | 8816 |
rs542057275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106987 | GTGGAAGCTGCAGTG[A/G]GCCGAGATTGCACCA | 8816 |
rs542094920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091320 | GTGTTTTATTGGTTT[A/C]TTTTTTTTAATGTCT | 8816 |
rs542135970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083643 | GGAAAATATAAAAGT[C/T]AAAAAATCTCCCCAG | 8816 |
rs542171014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084188 | CAAACTTTTGGTGTT[A/C]TTAAGGAGCTAATGA | 8816 |
rs542172167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093930 | AACACAGGCCACACT[C/T]TCTTGCATACAGAAA | 8816 |
rs542174778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074152 | TTAATTCAGCAACAG[C/T]CAAGAACTTCCCTAA | 8816 |
rs542196725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067167 | TCCCAAGTCTCTAGA[A/G]CTGTGCCTAGCACAT | 8816 |
rs542297155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147667 | TAGAAATAGGCTAAA[C/T]AGTTATCCCCATTTA | 8816 |
rs542324585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132031 | ACTACATTTTGTTTA[A/T]CTATTCATCCACTGA | 8816 |
rs542335076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089244 | TTCTCACTGTGTGCC[A/G]GGATTTGGAGACAAG | 8816 |
rs542384239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070990 | TTTAGTAAAGACAGT[A/G]TTTCACTATGTTAGC | 8816 |
rs542410888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096994 | GTAACAGTGCAGAAG[A/G]AGGGGGTGGGAGGAT | 8816 |
rs542465530 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146071 | ACTTTACAAACAAAT[C/G]CATCAATAATCAGTG | 8816 |
rs542608700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151609 | CACCCCCCCTCCCCT[C/G]AGCCAGGTTTCGGGG | 8816 |
rs542621191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144533 | GCCGAGATCGCACCA[C/T]GCCACTGCACTCCAG | 8816 |
rs542640055 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144128 | CTTGCCTTTCTATAC[C/T]ACAAATCTCATTGCC | 8816 |
rs542642657 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135429 | ATGACAAAATAGAAA[A/G]TACACATAAAACACT | 8816 |
rs542680007 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109445 | GAAATTGCCACCCAG[A/C]TCAAGATATAGAACC | 8816 |
rs542690592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110578 | CAGTCCTTTTCACTT[A/T]CTTAATAGTGTCTTT | 8816 |
rs542757344 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082078 | CCTTCTGTCAGAAAG[A/G]GAAAAACAATGTGAT | 8816 |
rs542807033 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137406 | TGATTATATCACAAA[C/T]ACGCTCCATCCATTC | 8816 |
rs542873271 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153627 | TTCCTCTGCTGGCCT[A/C]TGCCTTGGGCAGTCC | 8816 |
rs542884319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146838 | AGGCCAGAAGAAAAT[C/T]TGAAAACTGATTCCT | 8816 |
rs542884846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145149 | CGGCCTCCTGTGTAG[C/T]TGGGACTAAAGGTGC | 8816 |
rs542885251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104910 | ACTAAAAAGACTTAG[A/C]AGTCAAATCATCCAA | 8816 |
rs542921506 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104986 | ACAACTAGATATGAG[A/G]TGGTATTAAGGAATT | 8816 |
rs542922293 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091523 | GATAAAGAAACTCAC[-/TAT]TATTAAGTCAGAACA | 8816 |
rs542922608 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075330 | GCAGTACATTCATGT[A/G]AAGGATATACTTGCC | 8816 |
rs542923997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096244 | TGGGCTTTCTCTTTT[A/G]TTTTCCTAATGCACT | 8816 |
rs542941506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113742 | GGAATTCTAACAGAA[A/G]AGATCTGTAATTTCA | 8816 |
rs542943175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095369 | ATTAATGAAATACAT[A/C]TACCCCAACCTATCT | 8816 |
rs542981034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085739 | TTATATTCCCTCTAC[C/T]TTCTCTTTACAAAAC | 8816 |
rs543007436 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092229 | ATACTCGTCAAGACC[C/G]TGAGAAGTGGGTTGT | 8816 |
rs543014815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078071 | TCCCTAAGCTGCCAG[C/T]CCAAGTGATTTGATA | 8816 |
rs543037320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135348 | CGTTCACTCAGGAGT[A/G]CCTTGATGAAGCAGT | 8816 |
rs543120354 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149915 | ATAAACATGACACTA[A/G]TTTTAAACGTGGGAA | 8816 |
rs543142008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084880 | GATTGTTCAGTATGA[C/T]CCTCCGGATGACCCT | 8816 |
rs543206392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080356 | TACAAATATTTGCTG[C/T]GGGATACAAGGAAAT | 8816 |
rs543207037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072263 | ATTATGAGCATGTTA[C/T]AGGCAAAGGTAGAGA | 8816 |
rs543233502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067698 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 8816 |
rs543236966 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118449 | GTCAACTTTCAGGTT[-/A]AAAAAAAAGGTACTA | 8816 |
rs543248935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081176 | AAGAGGAAGAAAGAA[C/T]ACTTCATTCTTTCTA | 8816 |
rs543252812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110034 | ATACTGACACTCATT[A/G]TGGTTTTAATTTGCA | 8816 |
rs543408468 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078554 | ATCAATCCCCTATGT[A/G]TCCATCAACATCATT | 8816 |
rs543411422 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100099 | TACCCAATTATGCTC[-/A]AAAATAGATAGTGAT | 8816 |
rs543428664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143674 | GGGGATGTGAAACAA[C/T]GACAGTTACATTTTG | 8816 |
rs543523167 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098293 | AGTTCATTCATTCAG[G/T]CTTTATTCAAATATC | 8816 |
rs543558693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067759 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 8816 |
rs543569844 | snp | A/G | 1.66435e-05 | 0.0028847 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116547 | TACCTGTGGGCCACT[A/G]GCAGGCAGATAATCA | 8816 |
rs543589305 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070705 | TACCTACTTTAGAGG[C/T]CTTAGACATATTCCA | 8816 |
rs543661283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128020 | AAAAAGAAAAAAATC[C/T]TTATCAATTAGAGGT | 8816 |
rs543670740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061089 | TGGTTCACTGTAGCA[C/T]GACCTCCTAGGTTCA | 8816 |
rs543736353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108438 | ACGCAAGCTAAGGAG[C/T]CAGTGCAGTCAGAAC | 8816 |
rs543774998 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058507 | TTGGGTGACAAGAGC[A/G]AAATCCTGTCTCAAA | 8816 |
rs543775931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099875 | TCAACTGAGCCACTG[A/C]ACTGCAGCCTGGGTG | 8816 |
rs543811957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147878 | TTATGGGTTATTCTG[C/T]TAGCTCTATAAGTTC | 8816 |
rs543833263 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127043 | TTGCTGGTAGGATTG[C/T]AAAATGGTACAGCCA | 8816 |
rs543852764 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132324 | TCTTTGCTTGTTTGG[A/G]TAATAGTCATCCTAA | 8816 |
rs543856626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134357 | TTATAGTAATGTCAA[A/G]TTTCTTTCAAATGCT | 8816 |
rs543869219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065337 | CCTGACCTCATGATC[C/T]ACCCGCCTCGGCCTC | 8816 |
rs543871626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117322 | CTTACCTGCCTAACC[C/T]TAAAAACAAGCTTCT | 8816 |
rs543891126 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131164 | ACAAATTTATACATA[-/C]AAAGACAGATGCAAA | 8816 |
rs543943204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076565 | GTATGACTCCATTTA[C/T]ATGAGGCACTTAGAG | 8816 |
rs543949334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101232 | TATTAAAAAGAACAG[C/T]ATCAGACTGCAATGC | 8816 |
rs543954799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126302 | AGCTGGGATTACAGA[C/T]ACCCACCACCACGCC | 8816 |
rs543966322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114953 | CTTTCCACTGGAGAT[A/G]AACAGCTCAGTGCCC | 8816 |
rs543990893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106830 | GGATCACTTGAAGTC[A/C]GGAGTTCAAGACCAA | 8816 |
rs544054809 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154393 | GGGGAAAATAATAAT[A/T]ATTTTTTTTAAAAAA | 8816 |
rs544063406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141582 | AAGAATGAAAGGAAC[A/T]CTAATAATTACACTG | 8816 |
rs544071684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148505 | TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 8816 |
rs544172371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088664 | TGTTCATTCCTATTA[C/T]GGAAATTCTCAGATT | 8816 |
rs544177397 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056108 | ATGGTAGTTAATATC[C/T]GAGCCTATAGCTCCA | 8816 |
rs544266889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146766 | CTATTTGTTGCACTA[A/G]TAAATAGATCAAATA | 8816 |
rs544331894 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096768 | AGTCATTTGAGTTTA[A/T]CAGATGGCCTGGCTT | 8816 |
rs544359918 | in-del | -/T | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050485 | AGATACGAGTTTTGC[-/T]TTTTTTTTTTTTTAG | 8816 |
rs544428166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084149 | GGGGTCCTTATTCTC[C/T]CACCTACTAGAGAAC | 8816 |
rs544439738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142249 | AAGCTACAGTGAGCC[A/G]TAACTGCCCCTGCAC | 8816 |
rs544459449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131556 | CATTTTATTGTCACT[G/T]GTGAGGTAAGGATTA | 8816 |
rs544508776 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078569 | GTCCATCAACATCAT[A/T]CAGCCTTAACAAGGA | 8816 |
rs544509643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089299 | TTAGTCCCTAAGGAG[A/T]CAACAAAAAAGCCAA | 8816 |
rs544524856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123289 | CATGACAGCAGAAAC[C/T]TTGTCAGTTTTGTTC | 8816 |
rs544576571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138652 | ACTACTCACTAGTTG[C/T]AACCTACTGAGCAAA | 8816 |
rs544591846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072106 | CACAGCCCCATTTCC[C/T]TATTTGGCTTTTAAG | 8816 |
rs544650240 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139383 | CATCACCTATGTGTC[C/T]TAGCTACTTGGGAGG | 8816 |
rs544777723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074903 | AGCCGGTGTGGTGGC[A/G]TGTGCCTGTAATCCC | 8816 |
rs544804185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066382 | CCTCATAATCTGCCC[G/T]CCTTGGCCTCCCAAA | 8816 |
rs544819236 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110797 | GTGGGAGGACTGCTT[A/G]AGCCTTGGAGGTCAA | 8816 |
rs544826508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080233 | AAGCTATGCTGAAAG[A/G]ATCATCCCCTCCTGG | 8816 |
rs544832856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104869 | TCTTTAAAAAAAAAA[A/T]AAGTGAGAGACAGGG | 8816 |
rs544893535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103245 | CCATATATTTTTCTA[C/T]GGGTACATGTATAAG | 8816 |
rs544908638 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137296 | TATTAAGTTAGTGGA[C/T]GATGCATTGCCAGGT | 8816 |
rs544980918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113065 | TAATCAGCTTATTTC[A/G]GGGCAGCAGTGGGAC | 8816 |
rs545012753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150602 | TATTTTTTTTAAAGT[A/G]TGAGCTAGGCATGGT | 8816 |
rs545018365 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141475 | CGTCATTTACATTAG[G/T]TATATCTCCTAATGC | 8816 |
rs545033360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110520 | TGATCCAACTGCCTC[A/G]GCCTCCCACAGTGCT | 8816 |
rs545045021 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151857 | GCCTACACCGCCCGG[C/T]CGGAGCCCCGGCCTC | 8816 |
rs545145144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129574 | TTAATCTCCTAGTCA[C/G]TTCAGAAAGGCAGAG | 8816 |
rs545234948 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153514 | TTCCTCCCGCGGGGA[C/T]CCGCGGGCCGGCTGC | 8816 |
rs545248308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055810 | TGAGGTTTTTAGAAT[C/T]AGATGTGGGGAAATG | 8816 |
rs545269056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151435 | CCCAGAAGTTTCTGG[A/C]GAGCTGCTCACGGAC | 8816 |
rs545278455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086975 | CTTTTGTGTACATCC[G/T]ACTTTCAGCAAGATG | 8816 |
rs545282724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112212 | TTGCAGCAAAATAAA[G/T]AGTATATGCAGATTT | 8816 |
rs545307595 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065604 | ATGGCTTCAGAGAGG[-/T]TTTTTCATAGTTTCT | 8816 |
rs545378488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102344 | GAACTCCCGACCTCA[A/G]GTGATCCCTGCCTCA | 8816 |
rs545391482 | in-del | -/T | 0.262985 | 0.249663 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070791 | TAATTTTTATTTTTC[-/T]TTTTTTTTTTTTGTT | 8816 |
rs545394077 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134347 | GACTTAGACTTTATA[G/T]TAATGTCAAGTTTCT | 8816 |
rs545487392 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075181 | TATGTCTGAGGGATA[C/T]AGTTTAATCTGGTTT | 8816 |
rs545490301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099821 | GCATAGTGGCACATG[C/T]CTGTAGTCCCAGCTA | 8816 |
rs545503883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109883 | GGTGTTTAGCTTTAG[C/T]AGATACTGACAAATA | 8816 |
rs545527057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091498 | CTTGTATTTACCCAT[C/T]GACAGCCTTGATAAA | 8816 |
rs545529210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101010 | GTTTTCATGTATATC[A/G]TATCATCTAATCCTT | 8816 |
rs545537022 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114623 | AACTGTACTGATAGA[C/T]AAACATTTTAAAAAC | 8816 |
rs545623516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127967 | AAGGAAGTATTGTTA[C/T]ATCTTTTAGGTATTA | 8816 |
rs545672062 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094934 | ACACTGTGAGAAACA[C/T]GATTCCATTTTGGAA | 8816 |
rs545697270 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086622 | TGCATGGAGTTATTA[-/A]AAAAAAAAAAAAAAA | 8816 |
rs545699888 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099365 | TTTGTCTACCCATGA[A/G]ACCTGATCTCGAGGG | 8816 |
rs545709324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127245 | AGCAACCAAGATGTC[C/T]TTCAGTATGTAAATG | 8816 |
rs545710634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126081 | AATTTAACAAGATTT[C/T]ACAAGATCTACATAA | 8816 |
rs545711851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103279 | ATAAAAACCAAGAAG[A/T]AGTTCTGGAAGCATA | 8816 |
rs545713493 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093387 | ACAGACCTGAAAAGG[C/G]CCTCAAGATGCCTAA | 8816 |
rs545748318 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094380 | CACTATAGGAATTTG[G/T]TTGTGGGCTCCAGGA | 8816 |
rs545761349 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69149497 | TGTGCCCTGGAAAAG[C/G]GGATAGCTGTTGGAA | 8816 |
rs545783363 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142774 | ATGAGGAAAGACACC[-/T]TATTTGTTGACTGAA | 8816 |
rs545795883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084812 | GCAGATTCAGGAACA[C/T]TATTGTGTACAGATG | 8816 |
rs545804109 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120446 | ATGACTGTGATTCCA[A/G]ATGATGTGAAAGTTT | 8816 |
rs545819498 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059564 | GACAGAACCAAGGGT[C/T]GAGACTCAGCGGCCT | 8816 |
rs545824633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143016 | CAGAGTGTGAGGAAG[A/G]AGGAGACTTTAGATA | 8816 |
rs545938373 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075231 | TTCCTTTGGTCACAG[C/G]TTATGTTAGAAATGT | 8816 |
rs546003463 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069359 | CAAGGGCAGCCTTCA[G/T]GCAAGAACAACTCAA | 8816 |
rs546010080 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090445 | CCCTAAGACTCCAAC[A/G]TGAGTATAAATTCTG | 8816 |
rs546040094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069964 | GTCGTTGAGTAGCTA[C/T]TAAGTACTCTCACAA | 8816 |
rs546043308 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069787 | GCAGCAGTTAGTTTT[A/T]AAAAAAAAGTTTGTG | 8816 |
rs546108933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107927 | AGATGAATAAAACAC[A/G]CACCTGCCCTTAAAA | 8816 |
rs546234302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141371 | TTTCTTTTATTATTA[C/T]ACTTTAAGTTCTAGG | 8816 |
rs546247765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125222 | CATTCTGATGGACAG[C/T]TGAAGGGATTGTCCG | 8816 |
rs546250348 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143742 | TACTAAAACTGAAAA[A/G]AACAAAAACTTGAAA | 8816 |
rs546259750 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152057 | GCCTCGCAAGTTGCG[C/T]ATTCAAGTTCAGGCT | 8816 |
rs546272460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132797 | AATAATAAGAAAAAA[C/T]CCACAGGATTAGGAT | 8816 |
rs546288946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146378 | CTTTGATAGGTATCA[A/G]TTAGCTGACTAAAGA | 8816 |
rs546326472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083540 | TGTCTGAAGAAACAA[C/T]GGGAGGTGGAAAGGT | 8816 |
rs546337653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133430 | TAGAGAAATACAGAC[G/T]CAAGATTGCCAGATC | 8816 |
rs546373440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060113 | GACGTCAACAGGCCC[A/G]GAGAGGACACGTTAC | 8816 |
rs546396303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074430 | GAAACTAAGTAAAAA[G/T]AATGAAGAGGTATGA | 8816 |
rs546479687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117227 | CACTCAGTCATCTCT[A/G]CCATCAGGCAGTTCA | 8816 |
rs546511368 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126241 | CAGCTCACTGCAACC[A/T]CTGCCTCCCGGGTTC | 8816 |
rs546573089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088205 | CCTGTCCGCAACAAG[C/T]TGTGATCATTTGTAC | 8816 |
rs546616000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081632 | CTCTCAATAGATTTC[A/T]GGAAGGAACCACCAT | 8816 |
rs546629638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129087 | GCATTTATAGGATGA[C/T]TTCATTTTGCCTAGT | 8816 |
rs546654179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136289 | CCTGGCTAATTGTTT[C/T]CTTTTTTGTAGAGAC | 8816 |
rs546710727 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152991 | CATGCTGGAACCGCC[A/G]CCGCCGCCGCTCGCG | 8816 |
rs546721275 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109339 | CAAAACTCTGCCTCA[-/A]AAAAAAAAAAAAAAG | 8816 |
rs546730542 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109722 | TCCATTTTCCATTTT[C/T]TTTTGATGGATATTT | 8816 |
rs546739638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095699 | GGAAAGTGATTGAGC[A/G]TATCACTTCTAGCAC | 8816 |
rs546754945 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139703 | TGCCTACAATCCCAG[C/T]TACTCAGGAGGCTGA | 8816 |
rs546795111 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139919 | AAAGAAAGAGAAGGA[A/T]GGAAAGAAGGAAGGG | 8816 |
rs546796929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131128 | ATATGAATAGTATGA[C/T]ACAATTACACAAAAA | 8816 |
rs546809660 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078724 | AGACACGAAGTAGAA[C/T]GGTGGTTGCCAGGGC | 8816 |
rs546811760 | in-del | -/TTTTTACTT | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142871 | AATACACATATATTG[-/TTTTTACTT]TTAACTGGGCTAACA | 8816 |
rs546814558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086701 | TACTGCATTCCATAC[C/G]TTGGCTATACCCATA | 8816 |
rs546815929 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122628 | AGACTCCTAAAGCCA[C/G]CCTGTTCCTGTCTTT | 8816 |
rs546817176 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073008 | AAAAAGCTTATGTGA[C/T]ACTGGGTGTACTTTC | 8816 |
rs546845677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129780 | GCACAGGGACTTCTC[A/G]GGAAGGCTAGGCCTT | 8816 |
rs546861288 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064754 | CACCACTGACACTGA[A/G]TACATGATGAGAATA | 8816 |
rs546898288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056155 | ACATTCCTATTTTTA[A/C]CTAATGGGAATTGCT | 8816 |
rs546906627 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112594 | GATGATATATATGTA[C/T]ACACACACACACACA | 8816 |
rs546933992 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079154 | CAGTGGTCTTATCAG[A/G]GGTTTTACTATTTCA | 8816 |
rs547104265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069780 | GTGCCTAGCAGCAGT[C/T]AGTTTTAAAAAAAAA | 8816 |
rs547104819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119772 | CAAGAAAAACACTAA[A/C]TGATCATTGACAAAT | 8816 |
rs547114953 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132790 | AGGAAAAAATAATAA[C/G]AAAAAACCCACAGGA | 8816 |
rs547225508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120976 | AAGAGAAACTCAAAT[A/G]ACTCAAAACTCTTAC | 8816 |
rs547274822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110082 | AAAGTTCAGTACTTT[A/T]CAAATGCTTATTGGG | 8816 |
rs547312538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102931 | TACTACACTTTTATA[C/T]GACTGGCAGCACAGT | 8816 |
rs547314419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063649 | CCAAATATTTCTCAA[C/T]GTCTGTGTTTGGAGG | 8816 |
rs547424398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127445 | GGAAAAGACAAAATC[A/G]TGGAGACAACAAAAA | 8816 |
rs547435274 | snp | G/T | 2.0782e-05 | 0.00322344 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053807 | CACTAAACAATTTTT[G/T]TTTTTTTGTAAGGCT | 8816 |
rs547436001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090611 | AAACTATGACATTAG[A/G]AAGCCTCTAGCAACC | 8816 |
rs547444244 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091442 | GCAGAGCTAGGTGGC[A/T]CAGAACCATATCGTG | 8816 |
rs547465687 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148757 | AAAGCACCTTCACAT[A/G]TAACATTTCATTGAC | 8816 |
rs547485517 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118939 | TATGGTTCCTTCTCT[C/T]CTAAACTCTTGTTTT | 8816 |
rs547489812 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153926 | GATGAAGTCCCGAGA[A/G]GCACGAGGTACTTCT | 8816 |
rs547515874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069508 | CATTCTGTTGCTGAA[A/G]TGTGCAGCCTCAAAT | 8816 |
rs547557946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084913 | GGAATAATATTCATC[G/T]TGTGGGTAGAACAGC | 8816 |
rs547598334 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69115903 | TATATAATTTTCATA[C/T]AATTTTGGCAGTTCA | 8816 |
rs547627285 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125064 | AAGCCAAGTACAAAA[C/G]AGTAATATGCCAACA | 8816 |
rs547716632 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126782 | ACTGATCTTTGACCA[C/T]GGAGCAAAGACAAAA | 8816 |
rs547770979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149309 | AACCCAGTATCACAG[C/T]GATGCCCCTTTCTGG | 8816 |
rs547783539 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063601 | CCAAGTGCCTCCTTC[C/T]ACTCCCAACTCCACC | 8816 |
rs547916470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132981 | AGATAGATCTGTGTA[A/G]AAGACTTGGCCCAGT | 8816 |
rs547919559 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076401 | CCAAGGGTCTACTGA[C/T]AGATGAATGGATAAA | 8816 |
rs547962082 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088797 | ATAAAGCCCAATATA[A/C]GGAAAAGGCAGGCTA | 8816 |
rs547977998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089066 | ATCCTCCTAATTGGA[C/T]GAATTATTTAATTCA | 8816 |
rs547991690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134776 | GACTGAATTGGTTAA[A/G]ACAAAATAATGACCA | 8816 |
rs547991697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143165 | TTCACAATTCCACCC[A/G]TCATCCTCCACTTAC | 8816 |
rs548048612 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121929 | GTTTCAAATATGTGT[A/G]TGTGTCTGTGTGTGT | 8816 |
rs548067289 | snp | A/G | 0.000221527 | 0.0105221 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091839 | GCTGTTGAATCGTAC[A/G]CTCATGGCACTTTGG | 8816 |
rs548125127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092373 | TTTAATCCCAGCACT[G/T]TGGGAGTCTGAGGCA | 8816 |
rs548160893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083145 | AAAGACAACATAATC[C/G]AAAGGTAAAATCTTA | 8816 |
rs548203022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113475 | AGATACACAAGCCAT[A/G]CAATTTTACCTGCAG | 8816 |
rs548216301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067479 | CTCCCTAGTAGCTGA[G/T]ACTATAGGGACATGG | 8816 |
rs548256675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065663 | AATATAGCTGCTACT[A/G]AACAGTTTACGTACA | 8816 |
rs548265685 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081591 | GATACTAACTTGCTC[A/C/G]AGCATAGGAAGAGAT | 8816 |
rs548331126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067914 | TGCTGGGATTACAGT[C/T]CTGAGCCACTGCACC | 8816 |
rs548340109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082628 | ACCTGAGCAAGATGA[A/G]GGGCCATTAACCATT | 8816 |
rs548345009 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067425 | TTTAGCTCACTGCAA[A/C]CCCCCGCTCCCAGGC | 8816 |
rs548354275 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052981 | CTTTCACTATGCCTC[A/G]ATCGATCATGGGAGC | 8816 |
rs548374514 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147180 | GCTATTATTCAATGC[G/T]TAAAAATACTCTTTG | 8816 |
rs548395404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122959 | TATTGTTTTTTCCCA[A/T]TTTTACTTTTTACTT | 8816 |
rs548432143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116653 | CACCAGTCACCTCTA[C/T]TTACAAGGTCCCCAT | 8816 |
rs548454412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097369 | TGGCAATAATATGAA[C/T]GCCTCAGAACAATAG | 8816 |
rs548459684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105245 | ACAATCCAAACGGCT[A/C]TCATTAGATGAATGG | 8816 |
rs548518678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115551 | AATTTCCAGAGGAGC[C/T]AGCTAGCAATACACG | 8816 |
rs548549615 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060736 | AGGGTTTCACCATTT[C/G]GGCCAGGCTGGTCTC | 8816 |
rs548590545 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123336 | CACCTACATGAGTGC[G/T]CCAAGGAATGAGCAT | 8816 |
rs548708375 | snp | A/G | 1.64977e-05 | 0.00287203 | missense | DCAF5 | GRCh38.p7 | 14:69055329 | CAGTGTAGCCTGAGC[A/G]CTCGCTGACCCCAGC | 8816 |
rs548742759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104332 | ATAACTAGGCATTTT[A/T]AATTTCTTTATGGAT | 8816 |
rs548768968 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155007 | GTACTTAGGGAGTGG[C/G]GAGGAGTTTGAAGGG | 8816 |
rs548818874 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084417 | AGTTTGAAGAGGAAT[G/T]AAAACAAATTATTAA | 8816 |
rs548956850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151920 | GCCCGGGGGCAACCA[A/G]GCCCGTCTGGGCGAG | 8816 |
rs549017029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100329 | GCTTTGAGAAAAGTA[C/T]GAGAATAGGGAATTT | 8816 |
rs549063881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103664 | TATGCTATGGAAACT[C/T]GCTTGTATAGCTTGT | 8816 |
rs549123566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112442 | ACCCTATGTGATTTA[G/T]TAAGAGAGGGAACTG | 8816 |
rs549158350 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139234 | GTTCACACTTGTAAT[C/T]CCAACACTTTGGGAG | 8816 |
rs549160234 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103157 | ATACCAATGAGTGAA[A/G]AGTCCAGTTGTAGAA | 8816 |
rs549174862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138112 | GCTAAGCCATCAACA[C/T]AGTCAAGACACCTAT | 8816 |
rs549222932 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093593 | CCTATCCTATGGGAA[G/T]GGAAGCCCTGAAACC | 8816 |
rs549240036 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136035 | CTTCTACTTGTTTTG[A/G]TACAGTATTAAGGAA | 8816 |
rs549296471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128816 | ATATCTGCCAGGCCC[A/G]GTGGCTCATGCCAGC | 8816 |
rs549326563 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127983 | ATCTTTTAGGTATTA[C/T]AATGGCATTATGGTT | 8816 |
rs549348418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086069 | GAGCATTAAAATATA[A/G]TAGTGGGCTGGGCAT | 8816 |
rs549353042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126600 | GCAAAAGGCCCATAA[C/T]AGTCAACATGATTTT | 8816 |
rs549380022 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089870 | TATAATGCATAGGAC[-/AG]AGCTCCACACAACAA | 8816 |
rs549407180 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120450 | CTGTGATTCCAAATG[A/G]TGTGAAAGTTTTAAT | 8816 |
rs549415677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117650 | TCTTCATTTCACACA[G/T]CAGAGAGTCAAAGGG | 8816 |
rs549474259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092778 | AATTTAAATGCAGAG[C/G]AAGCAGTGCAACAAT | 8816 |
rs549513021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085169 | CCATTCTCTGAAACA[A/G]ATCTTTAATGTTTAA | 8816 |
rs549569362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150030 | TCTGAAGCAAACAGG[A/G]GGAACTTTCTGTTAA | 8816 |
rs549605310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128356 | CACACCCAGCTAATT[A/T]TTGTATTTTTTTAGA | 8816 |
rs549751200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059591 | GCCTTTCAGGATAAC[A/G]TAAGTGCAGGGTGAG | 8816 |
rs549806180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060709 | ACTAATTTTTGTAGT[A/T]TTAGTAGAGACAGGG | 8816 |
rs549820081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134730 | TTGTATGAGAAGTCA[C/T]AATACACTTTTTAGA | 8816 |
rs549876148 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059610 | GTGCAGGGTGAGGCA[-/G]TAATTCCAATTGAGA | 8816 |
rs549882911 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050490 | ACGAGTTTTGCTTTT[C/T]TTTTTTTTAGAAAAA | 8816 |
rs549901520 | snp | G/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091023 | AACTTCTATGGTTAA[G/T]ACAGAAAGGTGCAAG | 8816 |
rs549919083 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083893 | CCCCTGGGACTGACA[G/T]GAGCTTTTGAGGATA | 8816 |
rs549977992 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053618 | CACGTCTCACTAGAA[A/G]GGAGTCACTTGGGTT | 8816 |
rs550063886 | in-del | -/ACTCTGA | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083946 | CTTGTCAATGAAAAC[-/ACTCTGA]AGGCAATAAAAGAAA | 8816 |
rs550104243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142054 | AATCCCAGCACCTTG[A/G]AAGGCCAAGGTGAGA | 8816 |
rs550136496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061487 | GGCCAGGCTAGGACC[C/T]ACTTTTGCAGTTATA | 8816 |
rs550155854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147126 | CAGGAAATGACCATT[A/G]ATTAATAGGTTCAAA | 8816 |
rs550177432 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098418 | TCACCATCTTACATA[A/C]CATATATTTTTACAT | 8816 |
rs550184965 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088442 | GAGGTTCAGATATTT[C/T]ACACTTTATTCCCCA | 8816 |
rs550189170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108031 | TGGGAAGGAAATCAA[A/G]GACAAATACTGGCCT | 8816 |
rs550191514 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155285 | CCTCTTAAGCACATA[A/C]CCCCTTTACAGTTTT | 8816 |
rs550238845 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079354 | ATGCAGAAAATGCAT[A/T]GAATGTACAGGCTTC | 8816 |
rs550292752 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154349 | TGAGTAGAATCATCA[C/T]TGAAAGATGGGCTGT | 8816 |
rs550294740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146461 | TATGACATGATCTTT[A/C]TAATTTATCATAGCA | 8816 |
rs550318124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140077 | TCGAGACTAGCCTGG[A/G]CGACGTAGAGAAATC | 8816 |
rs550319802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116548 | ACCTGTGGGCCACTG[A/G]CAGGCAGATAATCAG | 8816 |
rs550358750 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117394 | AAAATGTTTAGAACA[C/T]AGAAAAGTTAAAAGA | 8816 |
rs550359839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142490 | TTCCACAGAAGCAGA[A/G]TGACGTTGTGGTGAC | 8816 |
rs550364203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067383 | GGGTCTCACTCTGTT[C/T]CCCAGGTTGGAATGC | 8816 |
rs550406015 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123831 | AGTCTCCTGAGTAGC[C/T]GGGATTACAGGCTCC | 8816 |
rs550592437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082462 | TCTGTGTAGAAAAAA[A/T]TCTATTAAGGAATAT | 8816 |
rs550631467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106182 | CTGCCTCAGCCCCCC[A/G]AGTAGCTGGAATTAC | 8816 |
rs550657102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087376 | GAAAGCAAGAAGAAC[C/T]TTTGGGCTCAGGTAG | 8816 |
rs550672191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072550 | GAGCTCAAGGCTGTA[C/T]GCAGTATGCTATGAT | 8816 |
rs550684948 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144576 | AGCGAGACTCCGTTT[-/A]AAAAAAAAAGATTAA | 8816 |
rs550713425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088267 | AATCTGGGTTCTAGC[C/T]CTGGTTTGCCTACAA | 8816 |
rs550716784 | snp | C/G | 8.24681e-05 | 0.00642085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075305 | CCAAAGGTCAACAGA[C/G]CCAGCAATAGCAGTA | 8816 |
rs550737528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132971 | AGGATTAATGAGATA[A/G]ATCTGTGTAAAAGAC | 8816 |
rs550745528 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082877 | TGAGACAGGTTATAC[A/T]CTGTTCCCCTTCATT | 8816 |
rs550766974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138018 | ATCCCCCACAGATGA[G/T]GGGGGACTACTGTAT | 8816 |
rs550789103 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074057 | TAACTTGTTTAGTAA[C/G]TAGACCACAGCAAAT | 8816 |
rs550790614 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138702 | CTTTGTTTACTTAGA[C/T]GTAAAATTAAAGACT | 8816 |
rs550815802 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110054 | TTTAATTTGCACTGC[C/T]CTCATGAGTGATAAA | 8816 |
rs550820882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122414 | ACATCGCAAGGCTGA[C/T]AGATGGTTTTGCCAG | 8816 |
rs550843402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124554 | TCCACCAAACTGATG[C/T]CTTAAGTGTGGCCCA | 8816 |
rs550880848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083040 | CCTTTACAACTGAAC[A/G]ATTACAAACCAGACC | 8816 |
rs550934735 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105204 | AATGTTAATGATAGT[A/G]TCATTCACAATAGCC | 8816 |
rs550947324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063334 | TGGGATAAATTCAAA[A/G]TTTCCACTGCACTGG | 8816 |
rs551004795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103022 | CAGCTACATTACCAG[A/G]TGACAGGAATTTTTC | 8816 |
rs551083944 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073678 | AGAAAAGAAAGCAGC[A/C]GGGAGAAGAAAAAAA | 8816 |
rs551105663 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097393 | ACAATAGCTTTAAAA[-/T]TTTTTTATAGTAACC | 8816 |
rs551114909 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086766 | ATGTCTGAGGGAGGC[A/C]ATTTATCCAAGGCCA | 8816 |
rs551116779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095555 | TTTTTTTAAGTACAC[A/T]CACACACACAAAAAC | 8816 |
rs551122511 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146283 | CAATGTCTAATGTGA[C/T]TAATGATCAGCAGCT | 8816 |
rs551131106 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121884 | ATAAAAAAAAACCAG[A/T]GTGTGCCACAAATAG | 8816 |
rs551132947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110944 | CTTAATTTTAATGAA[A/G]TCCAATGTGTCAATT | 8816 |
rs551205499 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103253 | TTTTCTACGGGTACA[C/T]GTATAAGCATATAAA | 8816 |
rs551279028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094789 | TCATCTAGGACTTTA[A/T]AAAATGTAGATTCTC | 8816 |
rs551343095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065533 | AAATAGGTACAGGCA[A/G]AATTATAGTGGCCAT | 8816 |
rs551365980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103537 | CACCATCTTGCATAG[C/T]CATAGTACAATATCA | 8816 |
rs551460566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110205 | CTTTATAAATTCTGG[A/G]TATTCTTAATGTATG | 8816 |
rs551478531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142758 | TCCCCATGTATAACT[A/C]TATGAGGAAAGACAC | 8816 |
rs551531129 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069625 | CTCTTTCTTTCTTTC[A/G/T]TTCTTTTCTTCTTTC | 8816 |
rs551543266 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053590 | CACAGAGCCTTGCGC[A/G]GCACACTACGCTCAC | 8816 |
rs551548231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144901 | CAAGTCACTTGTCTA[C/G]ATCTCAGCTCCCTTT | 8816 |
rs551560436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133039 | ATGTCAGCTAATTAT[C/T]ATGCTATTTGAACTC | 8816 |
rs551566983 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109282 | CCGGGAGGCAGAGCT[A/T]GCAGTGAGTTGAGAT | 8816 |
rs551571581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070401 | AATGTCTTGTATTTG[A/C]ATACACATTGTTTTC | 8816 |
rs551597202 | snp | A/G | 0.000297186 | 0.0121862 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152735 | GGGAGGGTGCGGGGA[A/G]GCGCGGGGAGGGGAA | 8816 |
rs551619540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149365 | TTTTCGGTTAAAGTA[A/T]CTTAACGTGTCAAAT | 8816 |
rs551656231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078885 | TACACTTTTTTTTTT[A/G]AGACAGAGTTTCTGC | 8816 |
rs551720507 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135479 | CAATACCTATTTTGT[C/G]AAAAAGTATCTATGA | 8816 |
rs551728309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127680 | AGTATATGTTTACCA[A/G]TTTTAACAAATTTAC | 8816 |
rs551739307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133652 | AACATCTACAGGCAT[C/T]ACTTCTGCTGACACC | 8816 |
rs551759203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092651 | AACTTGTTTATAATC[A/G]ATAATTTGTCAATCA | 8816 |
rs551820348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085992 | TTTGCCGTTTCACAC[C/T]ACTGTCGGCCTCAGT | 8816 |
rs551827224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133094 | TTTACTCTGGGTCAG[A/G]GACTATCCTAAGGGT | 8816 |
rs551830662 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068840 | GTGTCAAACCATAAA[C/G]AGGACCATCAAGGAT | 8816 |
rs551981145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083257 | GTGTACATTTTTCTG[A/C]GATGACTGTTTATAG | 8816 |
rs551982130 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056922 | CTTTGTTCCCTACCC[A/G]TAACTCTAGATGTGG | 8816 |
rs551988625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127486 | TGCCAGGGTTTGGAG[A/G]CAGGGGTTGAATATA | 8816 |
rs551993824 | snp | A/G | 0.000150397 | 0.00867041 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116333 | AAATGAGGCAGAGGA[A/G]AGTTTTAACACCTAT | 8816 |
rs552010787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126542 | TTCTCAGCAAATTCA[C/T]TTTATGCATATCAGC | 8816 |
rs552047026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085074 | ATTCAGTCTCAGCTT[A/G]AGAAATTGATTCAAA | 8816 |
rs552076634 | in-del | -/AC | 0.498323 | 0.0289051 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099251 | TGGGACTCTGTCTCA[-/AC]ACACACACACACACA | 8816 |
rs552086599 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078152 | GTTAAACTTTAATTT[A/G]AAAGTTTCCTAAACT | 8816 |
rs552106484 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086584 | TATGGCATGCCAGGC[C/T]CCAAAGTGGGCTTAA | 8816 |
rs552193681 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108231 | CAAAATAGTGCCAGG[A/T]GCCGGGGGACATGGT | 8816 |
rs552198235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106427 | AGGATGGAGTGCAGT[G/T]GTGCAATCATGGCTC | 8816 |
rs552213644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067989 | AGCAGGAGCAGAGAA[A/C]TAAAGGGGCTGAAAT | 8816 |
rs552236412 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128004 | CATTATGGTTATGTT[-/A]AAAAAGAAAAAAATC | 8816 |
rs552236684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059858 | TTCAGATCCCATGCA[A/T]ACTAGGGAGCAGTGA | 8816 |
rs552243777 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090211 | GAGAGACTTGATTGT[A/C]ATTTCCACAGCCAGA | 8816 |
rs552270418 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125238 | TGAAGGGATTGTCCG[C/T]CTTAGTAGCATAACT | 8816 |
rs552280829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083703 | AGCAATGCAGTCTCC[C/T]AATTCAGAATCAAAA | 8816 |
rs552298246 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066907 | GTCCTCCAAGAATGA[A/C/G]TACGTTTTTGACTCA | 8816 |
rs552312646 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099082 | ATGGTGAAACCCAGT[C/T]TCTACTAAAAATTTA | 8816 |
rs552344843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123563 | ACCCATTTTCAAGTG[C/T]ACAATTCAGTGGCAT | 8816 |
rs552370824 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052554 | CCTTCATAGATAACC[A/G]AGTGACTGCAACGCT | 8816 |
rs552393263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108605 | TTCAGCCAGGATGAT[C/T]ATAAGACAGACGATG | 8816 |
rs552408354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114289 | ATAACCAGGTTAAAT[G/T]TAACATTGTTTATAA | 8816 |
rs552464881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117491 | CTGCACTAAAGGCCA[C/T]GGTGGGTATGGCAGT | 8816 |
rs552468850 | snp | C/T | 0.00066981 | 0.0182882 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053843 | TGTAGCTTTTTGTTT[C/T]CCCTTTGTATTTATC | 8816 |
rs552470698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098137 | CTGTGACCCCACCTC[A/C]TAGGACTCTCTTACC | 8816 |
rs552494545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148030 | CGGAGTAACAATCCA[A/G]GTCAAATGCACATAG | 8816 |
rs552553191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068632 | GAACCTAGGAGACAG[A/G]AGTTGCGGTGAGCCG | 8816 |
rs552572591 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113364 | AGGGTAATCAGAACA[A/C]CAAGCAACTCTTATC | 8816 |
rs552583909 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116203 | TTGTCGCTGTCTATT[C/T]CTTGGAAACAAGCTC | 8816 |
rs552627788 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154403 | ATAATAATTTTTTTT[A/T]AAAAAAAAGATCGGC | 8816 |
rs552748983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148627 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 8816 |
rs552774297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095094 | CTCTTCAGATCAGAG[A/T]TATACTCCTGTCCTC | 8816 |
rs552794262 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050428 | CAAGCCTTGGTTGGC[A/G]AGAATTTTTCAGTTA | 8816 |
rs552813000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086920 | TCAGTGCTCAGGTAC[A/G]CCAGTGCTCAGCCTT | 8816 |
rs552866201 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065279 | TTTTTGTATTTTCAG[G/T]AGAGACGGGGTTTCA | 8816 |
rs552874457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121965 | TGTACCAGACTGCAA[C/T]GTGAAAAGTTTTCTG | 8816 |
rs552902800 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056617 | TCCCAGGCAATCTTC[C/T]TGCCTGACAGGCTGG | 8816 |
rs552906546 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150600 | GTTATTTTTTTTAAA[C/G]TGTGAGCTAGGCATG | 8816 |
rs552935806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112983 | CTGTACAATGAGGAA[C/G]TCTGATCATATTATA | 8816 |
rs552942142 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155156 | ACACATTCAAAACCC[A/C]CTCTAACTTCTTCCA | 8816 |
rs552966420 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074928 | AATCCCAGCTACTCA[G/T]GAGGCTGAGGCAGGA | 8816 |
rs552967280 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128085 | AATTTCCTTTAAAAC[G/T]TTCCAGAAAAAAAAG | 8816 |
rs552999748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137409 | TTATATCACAAATAC[A/G]CTCCATCCATTCTAT | 8816 |
rs553013746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129509 | AACGAGGGCTGGTGA[A/G]GCAAGGGAAAGTCAG | 8816 |
rs553101263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062966 | TCTAATCCATTTGCC[C/T]TCAGTTTCTATGATG | 8816 |
rs553247041 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074620 | AAGAAAGCCTCCCTT[C/T]AGTTAACATGACCAG | 8816 |
rs553267730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063984 | TTTGCTAATAAACCA[C/T]AAAAAAAGAGAGGGA | 8816 |
rs553275356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130161 | AAAAGCTGAGGTAAG[A/G]ATTTGCTTTGGGTTT | 8816 |
rs553298566 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136257 | AGTAGTTGAGACTAC[A/C]GGTGCACATCACCAT | 8816 |
rs553302531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062205 | TACAGGTACTGTCAC[C/T]ATGCCTGGCATCACT | 8816 |
rs553312722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119500 | TGATGTAAAAAAAAA[A/C]AACAACTGTGGCTAC | 8816 |
rs553313672 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152032 | CCGGGGGTCCCCCAC[A/C]CTACCGCCTGCCTCG | 8816 |
rs553410770 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103852 | AGGATTACATAAGTG[A/G/T]AATTATGCAGCATGT | 8816 |
rs553436220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109834 | ATTTCTCTTAGATAT[A/C]CTTAAGAGTGAGATT | 8816 |
rs553458669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099723 | CCAAGCAAGAGAATT[A/G]CTTGAGCTTAGGGGT | 8816 |
rs553465003 | in-del | -/ATAT | 0.449599 | 0.150533 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105915 | CCCTAATAAACTGTC[-/ATAT]ATATATATATATATA | 8816 |
rs553494546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151269 | GAGAAAACGATCTGG[A/G]GTACAAAAGTCAAGT | 8816 |
rs553546417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135069 | AGACACTTGAAAGGA[C/T]ACGATGTCATAATAT | 8816 |
rs553554234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144398 | TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 8816 |
rs553627537 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123516 | TTTTATGGTGGTAAA[-/AT]ATATATATATATACA | 8816 |
rs553648449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085271 | GCAATGAAGGCAAGC[A/C]GAAAAAGCGAGTAGG | 8816 |
rs553751902 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69149455 | TTCCTGATTTTCTCC[A/C/G]GTTTACTCAATATCT | 8816 |
rs553784816 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052667 | ACTAATGGGAACCAG[A/G]AGTCATAAGCCAGAG | 8816 |
rs553809756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150121 | TGTTCAAGGAACAAA[C/T]AGGAAAAGCTAGGTG | 8816 |
rs553940292 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139827 | TAAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAGA | 8816 |
rs553954637 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052135 | TTTCATACCCCAGCC[A/G]CATTACACACACCAG | 8816 |
rs553962083 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089246 | CTCACTGTGTGCCAG[G/T]ATTTGGAGACAAGAC | 8816 |
rs553971195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077876 | AGGTGGGTTTAAAGA[C/T]GAAGAAAATGCTATC | 8816 |
rs554042765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083938 | TATGTAATCTTGTCA[A/G]TGAAAACACTCTGAA | 8816 |
rs554053740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084688 | TTCATCTTGTATGTC[C/T]GTGAAATACCACTAT | 8816 |
rs554138508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125109 | CATTGAGCTAAGATT[C/G]AAAAGCAAGCAGTAA | 8816 |
rs554151364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057959 | TCTCATATGTGTAAA[C/T]GAGAATGATACCAAA | 8816 |
rs554199568 | snp | A/T | 0.0599851 | 0.162463 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141139 | ACTCCATCTCAAATT[A/T]AAAAAAAAAAAAAAA | 8816 |
rs554213634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142121 | GCAAAATAGTGAGAT[C/T]CTGTCTCTACAAAAA | 8816 |
rs554223624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098659 | GAGGCCGAGACAGGC[A/G]GATCACGAGGTCAGG | 8816 |
rs554229524 | snp | C/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155332 | AAATTGTCCCATTTA[C/G]CTCAGCATAAAAATA | 8816 |
rs554236609 | snp | A/C | | | intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69149476 | CTCAATATCTGCTGG[A/C]CTCACTGTGCCCTGG | 8816 |
rs554238662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066206 | GTGGCATGATCTCAG[C/T]TCCCTGCAACCTCCT | 8816 |
rs554266276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089827 | ACCGGCTTCTAGTAG[A/G]AAGAGGCTAGGGATA | 8816 |
rs554268327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148322 | AATACAATGTTGTTC[C/T]CCATCCCTCAAAGGA | 8816 |
rs554315187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068233 | CAGTGGCCCATAGAG[A/C]TTTACATGATGTCTT | 8816 |
rs554347814 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050627 | TTCCCTCTGTTCCAA[C/T]TAATAAAATTATCAG | 8816 |
rs554350373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060066 | TCTTGTAAAGGAGAT[A/T]CCCAAGCAGAAAGCT | 8816 |
rs554402191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073879 | TACTTCTCAACGAAT[A/C]AAGCTAGGAATTACA | 8816 |
rs554420404 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154557 | GCAAACATTACTAAA[C/T]AGAAACCAAATTCCA | 8816 |
rs554473498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133919 | TTCTCCAAAATCAGA[C/T]GACTAATAGCAGTGG | 8816 |
rs554478059 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69055977 | ATAATAATCCTGGAG[-/AA]AATAGAGGATGACTT | 8816 |
rs554483823 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147726 | CTCTCCCCATTCACA[A/T]CTCCTACATAATTAA | 8816 |
rs554496538 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080314 | TAAGAGGACCACCAG[C/G]ACACTGCAGGTCTAG | 8816 |
rs554516568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097727 | CAGCAGCTGGGATTA[C/T]AGGCGGGCACCACTA | 8816 |
rs554577299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074701 | CAAGAATATGAAGAT[A/G]GATAATAAAAGCAAA | 8816 |
rs554647313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113759 | GATCTGTAATTTCAT[C/G]CCCAAACTCCAGTGG | 8816 |
rs554658143 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112805 | ATTTATTATTATGAG[A/G]CACTGAGAGGTGAAG | 8816 |
rs554679599 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153301 | CGTCGGCGCCCCTCC[C/T]CTCCGCGGGGGGCTG | 8816 |
rs554735805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138536 | GTAAGCCACTTAGGA[A/G]TTTAACACTTTACTT | 8816 |
rs554746869 | in-del | -/TTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128194 | AATTTTTTCTTCTTC[-/TTT]TTTTTTTTTTTTGAG | 8816 |
rs554748341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139362 | GGTGATGCACACATA[G/T]GTGTACATCACCTAT | 8816 |
rs554857891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114518 | GATGCATATGCATAG[C/T]CGTATATACATTACA | 8816 |
rs554865572 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137408 | ATTATATCACAAATA[C/T]GCTCCATCCATTCTA | 8816 |
rs554868858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145940 | CTTTGCCTTGATCAA[C/T]GCATGAGAAAATAAA | 8816 |
rs554879349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058475 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 8816 |
rs554934122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079837 | AAGTTAAACAAAAAA[C/T]AACATATATATATAT | 8816 |
rs554951620 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095863 | CCTCATTGTTTCCAC[A/G]TGAAAGCTCTATAAG | 8816 |
rs554970876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056436 | TTCAAACTCAGGTCT[A/G]CCTGACTTAAAGGCT | 8816 |
rs555049656 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126265 | CGGGTTCAAGCAATT[A/C]TCCTGCCTCAGCCTC | 8816 |
rs555074561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065125 | TTTTTTGAGACGGAG[C/T]CTTGCTCTGTTGCCC | 8816 |
rs555105569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088317 | TGTGACCTCTCTGAG[A/T]CTCAGTTTACTCATC | 8816 |
rs555113392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140968 | GTGAAACCCCGTCTT[C/T]ACTAAAAGTACAAAA | 8816 |
rs555156128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103160 | CCAATGAGTGAAAAG[C/T]CCAGTTGTAGAATGA | 8816 |
rs555161261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081191 | TACTTCATTCTTTCT[A/G]GATAAATACTTCATT | 8816 |
rs555183892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121327 | TCCAGGCCAAACTAA[C/T]GGATGAGTATGAGAG | 8816 |
rs555194631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094044 | TGAACTCAAAAACAA[G/T]GAGAGGCTTTCAATC | 8816 |
rs555220746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086909 | TATAAGAGATCTCAG[C/T]GCTCAGGTACGCCAG | 8816 |
rs555221636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070821 | TTTTCTTTTTTGAGA[C/T]GGAGTCTCCTCTGTC | 8816 |
rs555247821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129395 | GTTGGCAGAAAAACA[A/G]CCAGTACAAATTGAG | 8816 |
rs555308630 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066259 | CCTGCCTCAGCCTTC[C/T]GACTAGCTGGGATTA | 8816 |
rs555335529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137361 | TTACCTCTTCTGCCA[C/T]AGAGAACTAACCTGG | 8816 |
rs555342650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136600 | TCACTTATGAAAACT[A/G]ATATTTTTTCAGTTT | 8816 |
rs555396139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144313 | CGCGGTGGCTCACGC[C/G]TGTAATCACAGCACT | 8816 |
rs555408275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144942 | GAAAATCCTTCCATT[G/T]CTCCGATCCCATGCA | 8816 |
rs555431175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078252 | AAGAAGTAGAACATG[A/G]CCATATACAAATGGC | 8816 |
rs555511651 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086517 | AGGCTGGAAACCAAC[A/G]GTTGAATTTCCCCCA | 8816 |
rs555517035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127647 | GAACATTGGGACTCT[A/G]AGTGTTTATGATGTG | 8816 |
rs555601343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128699 | CTTGAACCCTGGAGG[C/T]GGAGGTTGCAGTGAG | 8816 |
rs555631276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061106 | ACCTCCTAGGTTCAA[A/G]CAATCCCTCAGCCTT | 8816 |
rs555640684 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100348 | AATAGGGAATTTAGA[A/G]AGCCTCTTAATGGAA | 8816 |
rs555650743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071013 | ATGTTAGCCAGATTG[G/T]TCTCAAACTCCTGAC | 8816 |
rs555668189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061934 | CTCAGGCAGAAGGAT[C/T]GCTTGAGCCCAGAAG | 8816 |
rs555708274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127018 | GTGGAACAACACGCA[A/G]TCTCATTCATTGCTG | 8816 |
rs555780610 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111322 | TAAGAGCAATTTCCC[C/G]ATAGTAGGAACTTGC | 8816 |
rs555788885 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125406 | AAACTGGTAATGGCT[C/T]AATGTCTAGAAGATG | 8816 |
rs555813824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125952 | CTTTAAAAAAAAATA[C/T]AGAAGTGATTTTAGC | 8816 |
rs555847627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077747 | CAAAAAGTGTAAGTC[C/G]AACATACACACAACC | 8816 |
rs555875389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084614 | CCTTCTGAAAAGAGA[C/T]TCCTTCTACTCTTTA | 8816 |
rs555875587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098406 | CTACTGCATCAATCA[C/G]CATCTTACATACCAT | 8816 |
rs555911754 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154719 | CTCAGGATGCCTTCT[A/G]ATAATCCTTTGTGTT | 8816 |
rs555928178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142257 | GTGAGCCGTAACTGC[C/G]CCTGCACTCTGGTCT | 8816 |
rs555932388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149386 | CGTGTCAAATAACCA[C/T]TTCTCCACTTGTTGC | 8816 |
rs555942233 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142866 | CAGTAAATACACATA[C/T]ATTGTTTTTACTTTT | 8816 |
rs555944341 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151110 | AACTGGGAGCTAGGT[C/G]TATAAAGAAGAGGTC | 8816 |
rs555974764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102044 | AAATATTACACACAG[C/G]CTACGCTACATTTAT | 8816 |
rs556010654 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063766 | TTTTGTCTCATGGAA[A/G]AGATACCTCCTTATT | 8816 |
rs556024214 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122140 | ATACAGGAAGAAAAA[C/T]AAGGAGTTATTTTCG | 8816 |
rs556068640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148937 | CCACACCACATTGTG[C/T]CTCCACATTCCACAT | 8816 |
rs556085702 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059892 | CCATAGTTCAGTCTG[C/G]ATAACCTCACAGATA | 8816 |
rs556171503 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089588 | CTTTTATAATTATAT[A/C]TAAACTGAAAGACAG | 8816 |
rs556176856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089214 | CAAGATTTACTTCAA[C/T]AAATTTTTATTGTGT | 8816 |
rs556198241 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052005 | TCTGATTACAAATCC[A/G]AAGTAATTCTAATGT | 8816 |
rs556209454 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106909 | TAACCGGGCATGGTG[G/T]CACATGCCTGCAGTC | 8816 |
rs556216241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067679 | AAGATGGAGTCTCAC[C/T]AGGCTGGAGTGCAGT | 8816 |
rs556284888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140319 | ACATTCTACAGCCAT[A/G]TACCTGAAAAACTAC | 8816 |
rs556320687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059363 | AGAAAGAAGGGGGAG[C/T]AGAGAGAGAAAAGCA | 8816 |
rs556377935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124931 | AAAAGTTAAAAGAGA[A/G]GCACACGTTTCTTCT | 8816 |
rs556499784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064939 | ATATAAAGAATCAGC[C/T]ATCATAGAACTAAAG | 8816 |
rs556543526 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132594 | ATCATATATAAATTT[C/G/T]GGAAATTTCATATTC | 8816 |
rs556596721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074952 | GGCAGGAGAATTGCT[C/T]GAACCCGGGAGGCAG | 8816 |
rs556634681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072837 | GTGATACAGAGAAAA[C/G]AAACCCTCAATTACA | 8816 |
rs556674430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075613 | CAACCTCCAGAGTAG[A/C]TGGGACTACAGGCAC | 8816 |
rs556680610 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084395 | GCTGATCGTATCTTG[G/T]ATGTTGAGTTTGAAG | 8816 |
rs556708317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092333 | CATCAGTAAAAACAA[C/T]AGGCCGGGTGCAGTG | 8816 |
rs556722395 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154479 | ACTTTTTGTTCAGTG[A/G]CAATACGATTAATCG | 8816 |
rs556814445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138451 | TCATCTGTAAAATAA[A/T]AGGGCATCACCAATT | 8816 |
rs556844835 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113744 | AATTCTAACAGAAAA[A/G]ATCTGTAATTTCATC | 8816 |
rs556862280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066038 | CAGGAAAAAGGATCT[C/T]ATTCCTGAGCTGCCA | 8816 |
rs556870884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081747 | TCCATTGACCTTTAT[A/G]GAAAATGTGTGTGTG | 8816 |
rs556879052 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105034 | GGAATAATATTGTGG[C/T]TATGTTTTTTTTTTA | 8816 |
rs556913944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139320 | GAGACCTTGTCTCTA[C/T]GAAAAAATTAAAAAT | 8816 |
rs556926035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131208 | GTCATCTCTTGCAGA[C/T]AGCAATTTTACTTAA | 8816 |
rs556967550 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143999 | GAATTCTATTTTTCC[A/G]CTAATGCATTGCCTG | 8816 |
rs556980566 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140349 | CAATCCCTGAAAATT[A/C]TTCTCCGGGCCACTT | 8816 |
rs557007694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122052 | AAAAGACACACACTA[C/T]CCTAATATATAATAC | 8816 |
rs557091020 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153058 | CTCCCCCCACCCGGC[C/T]CTCCCCCCGCGCTGC | 8816 |
rs557122973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111772 | ATCATCTAAATGAAA[C/T]AAATGAAACCTTGTC | 8816 |
rs557154400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145835 | AAAGCAATTAGTTTC[C/T]TCTTTCTTAAGACCA | 8816 |
rs557179507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113662 | ATCTATTGCAACTCA[A/G]CATAACTAATCCTAC | 8816 |
rs557212118 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154153 | CTAGTGGGTGTTAAA[C/T]GCTTTGGAATTCTAC | 8816 |
rs557224673 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067761 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8816 |
rs557260774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152228 | GCCCCAGTCACTTCC[C/T]CTCTGCAGACCCCGC | 8816 |
rs557284836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108235 | ATAGTGCCAGGTGCC[A/G]GGGGACATGGTGAGT | 8816 |
rs557297634 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069504 | GTCTCATTCTGTTGC[C/T]GAAGTGTGCAGCCTC | 8816 |
rs557313131 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110529 | TGCCTCGGCCTCCCA[C/G]AGTGCTGGGATTACA | 8816 |
rs557436901 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088001 | TTGTAATATTTTAAA[A/G]CCAAGAGACCTTACA | 8816 |
rs557440998 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076215 | AACGGTGCAACTGCT[A/G]TGGAAAACAATATGG | 8816 |
rs557516516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071878 | CATATAAAAATGAGA[A/G]GTACCAAATAGTCCT | 8816 |
rs557521898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145075 | TTTCTTTAAATTGAT[A/T]TGCATGATGATGGCT | 8816 |
rs557529237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128001 | TGGCATTATGGTTAT[A/G]TTAAAAAAGAAAAAA | 8816 |
rs557568600 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148167 | TAAGAAAAAGGAAAA[C/G]CATAAGAGGAGGCAA | 8816 |
rs557578588 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131843 | ATTTTCATATCGTTG[A/T]GCAACCATCACCACA | 8816 |
rs557620808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079198 | GTGCTTTCCTATTTG[C/T]TCGGCTATTCATCAG | 8816 |
rs557626164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087004 | TGTAGGGACTATTAG[A/G]CCAGGCATCATATGA | 8816 |
rs557630119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095748 | AGCTTCCAAGATCAG[A/G]CTCTGTGGACCTAGA | 8816 |
rs557651382 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067582 | ACTCTTGGGCTCAAA[C/T]AATCCTCCTGCCTTG | 8816 |
rs557667994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136532 | AATGACACTCTTCTC[A/G]CTATTTTTTTTTAAT | 8816 |
rs557689356 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095269 | AAGTGGCCACCAATA[C/T]ATTCAAATGAGATGA | 8816 |
rs557744734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150355 | TACCCAGAATCGAAA[C/G]GTCTGCCAGAGCCTC | 8816 |
rs557768431 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070478 | GTAGGAGACATTTTA[C/T]GTAAGAAACTGACGC | 8816 |
rs557784843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086328 | GAGCCACTGCACTCC[A/G]GCCTGGGTGATAGAG | 8816 |
rs557825957 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084541 | ATTGTATGTTGGTGT[G/T]GATGACGATAAAGCT | 8816 |
rs557844221 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114702 | TATTTTTTTCTGCAT[-/A]AAACCCCCAAACCAA | 8816 |
rs557869968 | in-del | -/AAAAAAAAAAAAAAA | 0.499824 | 0.00938333 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110877 | CCAAGACCCTGTCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 8816 |
rs557904797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060784 | TGATCCACTTGCCTC[A/G]GCCTCCCAGAGTGTA | 8816 |
rs557930958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149529 | AGAAAAGTGATGTAT[G/T]ATTAACTAATAGTAC | 8816 |
rs557934977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069977 | TACTAAGTACTCTCA[C/T]AATAATCCTAAGAAA | 8816 |
rs557941864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061828 | GTGTCTAGAAGACAA[C/T]CTCTGTTTCAAAGCC | 8816 |
rs557949740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083570 | TTAAAAAATCAAAAC[A/G]TTCTATGAATGTGGG | 8816 |
rs558019414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068269 | AGGATACTCAATAAG[C/T]GAACAAATTGAAGTT | 8816 |
rs558047010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078369 | GAATGGTTACTATGA[A/G]AAACAAAACAAAGAC | 8816 |
rs558056280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060236 | TCCAGCAGCAGAATC[A/G]GGATGCTTGCTGCCT | 8816 |
rs558066482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068882 | GGACAGAGCAGTGAC[G/T]GCCTCCTGGAGACCA | 8816 |
rs558067630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135889 | CGATGTATGATGTTA[C/T]AAAATGATGCATGGG | 8816 |
rs558111634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124878 | TTTTTTTTTAATTAG[A/G]TAAGTATTTCTCTAT | 8816 |
rs558114074 | snp | A/G/T | 6.62411e-05 | 0.00575473 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119264 | GACATCTGATCATTC[A/G/T]TGCAAGGTGGTCCCT | 8816 |
rs558190791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134832 | ATACATTGGTCCAAG[A/T]GTAAATAAGCTGGTT | 8816 |
rs558194677 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126295 | CCTGAGTAGCTGGGA[G/T]TACAGACACCCACCA | 8816 |
rs558212971 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126417 | CCACCTAGGCCTCCC[A/C]AAGTGCTGGCATTAC | 8816 |
rs558216814 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144964 | TCCCATGCAGAAAAG[A/T]GAAGATATAAAAGGG | 8816 |
rs558226357 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122106 | CTATGAGAAACCAGT[A/G]ATTCCACAGCTCAAT | 8816 |
rs558242799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058614 | GCGTGGTGGCTCACA[C/G]CTGTAATCCCAGGAC | 8816 |
rs558303969 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146846 | AGAAAATTTGAAAAC[G/T]GATTCCTCAATTACC | 8816 |
rs558343878 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052795 | ACAGCCTCTATCAAC[A/T]GCAAGTCTGAGGGAA | 8816 |
rs558349663 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128860 | GAGGTGGGAGGATCC[A/G]TAATCCCAGTACTTT | 8816 |
rs558360207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108982 | CCACTGGAATCGTAG[C/G]GAAGAAGATAAATAC | 8816 |
rs558378486 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063364 | GTAATGGTATCACAT[C/T]CATCCAGAACACATG | 8816 |
rs558493867 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146182 | TAGGAAATCTTAGCT[A/T]TCAAAAACACATTGG | 8816 |
rs558532910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059310 | TGACAATAGGGACTC[G/T]TCTCCTAGCCAGGAA | 8816 |
rs558561939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067611 | TGGCCCCCGGAAGTG[A/C]TGGGATTACAGGTGT | 8816 |
rs558615761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106798 | TAATTCCAGCACATT[G/T]GGAGGCTGAGATGAG | 8816 |
rs558630915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095915 | GAGGCACTACTATCC[C/T]AACTCACAGACATCA | 8816 |
rs558632885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105408 | CAGAAGGTCACATAT[C/T]GTGATGGCCAATATT | 8816 |
rs558705714 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69055841 | CATGGTCTAGAACAC[A/T]GTATTAGCCTAGTGT | 8816 |
rs558716959 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061518 | AAAACATTTCCTGGT[A/G]GAGGTGAGTTCATTC | 8816 |
rs558721549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131536 | ATTCAATCACTTACA[A/T]ATCTCATTTTATTGT | 8816 |
rs558828465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089939 | GGAAACCATGGTCTA[A/G]GTGCTTACATGTTGG | 8816 |
rs558844146 | in-del | -/TTTA | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080760 | CTATGTTTCATATTT[-/TTTA]TTTCCTTTTATGATG | 8816 |
rs558854034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139518 | AGAAAGAAAAGAAAA[A/C]AAGAGAAAAGGAGGC | 8816 |
rs558859778 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050704 | ACAAATAAATACCTC[A/C]TCCTACCCTGCATTT | 8816 |
rs558896200 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098932 | AAAAGAAAAAAAAGA[A/C]AAACACTGACTTAAA | 8816 |
rs558954145 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154052 | CTCGAGTGGGGAGCA[C/T]TGAGGTTGGACAGCT | 8816 |
rs558965996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113582 | GGCTTGTCCTCCCAA[C/G]AGATTTAGAGTTGCC | 8816 |
rs558969584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088520 | CCTAGTGAACCTAGG[A/G]TAGTTTAAAAAGAAG | 8816 |
rs559008077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082057 | ACAGCTCTTATTTTC[C/T]CCTGACCTTCTGTCA | 8816 |
rs559008490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078726 | ACACGAAGTAGAATG[A/G]TGGTTGCCAGGGCCT | 8816 |
rs559046045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079561 | TTATGGCATTTCACG[C/G]TTGTCTGCTGGATGC | 8816 |
rs559053304 | snp | C/G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153419 | GCGCCGGGCGGAGAC[C/G/T]CCTCTGCACCCCAGC | 8816 |
rs559053620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057531 | ATGCTGGCTTAACTC[C/T]TTACTAAGCCCATTT | 8816 |
rs559115189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103484 | GAAATGTACAAGAAC[A/G]TCCTGTGCATCCTTT | 8816 |
rs559150038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094758 | TTCTGGCTTCAAGTG[A/T]AAGATGCATGAAAAA | 8816 |
rs559151950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104135 | AATTGCTGGGTCATA[C/T]GGTAAGCTCATCTTT | 8816 |
rs559152952 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143814 | TGGTTATAAAAAAAT[A/C]TTTTTTCACCCCTAG | 8816 |
rs559224283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089157 | ACAGTTAGAGAAGAC[G/T]TAGGCCCACAAAGCT | 8816 |
rs559239673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147324 | AAGGTATCAATCTCC[C/T]GAAAGCCTTTTGTGA | 8816 |
rs559274720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137628 | CCACCCACCAGCAGA[C/T]GTAAACAGAGATGTC | 8816 |
rs559340372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110815 | CCTTGGAGGTCAAGG[C/T]TGCAGTAGCCATGAT | 8816 |
rs559352361 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135458 | CTTCTGCTGCACACT[A/G]AAAAACAATACCTAT | 8816 |
rs559380097 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121455 | AACCATGTGAAACTG[C/T]TACTTTTTAAAGTTG | 8816 |
rs559383367 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105409 | AGAAGGTCACATATC[A/G]TGATGGCCAATATTA | 8816 |
rs559384973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128750 | TCCAGCCTGGGTAAC[A/G]GAGCAAGACTCCATC | 8816 |
rs559387909 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063202 | TAAAGTCAAGAGGAC[A/G]TCGATAGAAAGCTGT | 8816 |
rs559399709 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115133 | TGCAGATGAACACAG[A/T]TGTCTTCTTGGCAGA | 8816 |
rs559455517 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052540 | CTGTTTTGCACAACC[C/T]TTCATAGATAACCGA | 8816 |
rs559469169 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151673 | CACCCGCCCCTGCCC[G/T]GGGCCCGCGACCCCA | 8816 |
rs559481632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112119 | TTTTCAAACTCTAGT[A/G]TATCAGGTAGACCAA | 8816 |
rs559522076 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136721 | TGTCACAACTGGAAA[G/T]ATGCTAATGGCATAC | 8816 |
rs559523973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128122 | GATAGATGATTAATA[C/T]GGACAATTGCTATAG | 8816 |
rs559627123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061184 | TTTTGTAGAGACCAC[A/G]TCCCACTATGTTGCC | 8816 |
rs559737625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142364 | CTTTCCCTAAATCTC[G/T]GATTTAAGAAAACTG | 8816 |
rs559776943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109201 | AAAAAGAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 8816 |
rs559788272 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098668 | ACAGGCGGATCACGA[G/T]GTCAGGAGATCAAGA | 8816 |
rs559794747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060399 | AAAAAGTAAAAATGA[C/T]TTCCTCATTCTAGCC | 8816 |
rs559804051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093322 | ATTGTCATGGATAGG[C/T]AGTGATCCCAGTAGT | 8816 |
rs559815335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101382 | AGGCACTGTGTCACA[C/T]ACATGGATTCAAAGA | 8816 |
rs559829746 | snp | A/C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065563 | TTTGTTTAAGGTAAC[A/C/T]AAGACTGTGTACAAT | 8816 |
rs559841695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108547 | GCAAAGATGTTTATG[A/G]CAGAGGGAGGGAGAG | 8816 |
rs559844431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150597 | TTTGTTATTTTTTTT[A/T]AAGTGTGAGCTAGGC | 8816 |
rs559884232 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056421 | GCAGCAGAGCTAGGA[C/T]TCAAACTCAGGTCTG | 8816 |
rs559885303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069242 | TCAGCCTACTGCCAG[C/T]GGGGGTGGTTACAGT | 8816 |
rs559919148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087702 | CATCTGGCAATGTTA[C/T]GTGAATGTATCTATC | 8816 |
rs559920439 | in-del | -/TC | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067652 | ATCCAGCCCAGATAT[-/TC]TTTTTTTTTTAAGAT | 8816 |
rs559937716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091355 | CACCAGCAGGCTAAT[C/T]TTCCATGGATTCCCT | 8816 |
rs559963497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092546 | CCACTTGAGCCTAGG[C/G]GGTTGAAGCTGCAGT | 8816 |
rs559977941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149842 | AGCCTCAGAATACTG[G/T]GCTCCCCCACTCAGG | 8816 |
rs559980026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130853 | GCTCTGGAATAAAAG[A/G]ACTTGATTCAAATCT | 8816 |
rs559996113 | snp | A/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060498 | GAAGTTGGACTAAGG[A/G/T]CAAATAAAAATACTG | 8816 |
rs560039357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143270 | ATCAGATCCTTTAAA[A/T]ATGCATATAACATTG | 8816 |
rs560072089 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095970 | AGAGAGAAAAGCAAG[A/G]TCCTTTCTATGGGAG | 8816 |
rs560161778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099068 | CCATCCTGGCCAACA[C/T]GGTGAAACCCAGTCT | 8816 |
rs560171239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084189 | AAACTTTTGGTGTTC[A/T]TAAGGAGCTAATGAG | 8816 |
rs560181236 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074407 | CTAAGAAAAAGAAAA[-/G]GGGGGGGGAAACTAA | 8816 |
rs560195517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082291 | GAGAAATTTCACTGC[C/T]TCCCAATAAAAGCAT | 8816 |
rs560202525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090148 | AAGAAGTTGACAAAG[A/G]ATAGGAAATCAACAA | 8816 |
rs560302417 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117487 | CAATCTGCACTAAAG[A/G]CCACGGTGGGTATGG | 8816 |
rs560307871 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107137 | TGGACTTGGGGAATA[C/G]GAAAGGAAGAATATG | 8816 |
rs560374902 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120804 | AGAATAAGATTCTAC[C/T]CTGTCCTTGAGAACT | 8816 |
rs560415534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132033 | TACATTTTGTTTATC[C/T]ATTCATCCACTGATG | 8816 |
rs560452406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059411 | GAATGTGGTGGCTAA[C/T]GCTCTTTGAGCCACT | 8816 |
rs560454583 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155033 | AAGGGAAAGGTCGTG[C/G]TTTCCGGTTTGGATA | 8816 |
rs560471580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076828 | ATTTTAATGCAGAAC[A/G]TAAAAACTAGGAGCT | 8816 |
rs560500640 | snp | C/T | 5.02553e-05 | 0.00501254 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116321 | ACATTACCTGAGAAA[C/T]GAGGCAGAGGAAAGT | 8816 |
rs560517332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056763 | GTGGGAATTCTCCTG[A/T]GTCCCATTCCTGCCA | 8816 |
rs560544306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124215 | ATGCATATTTTGTTT[A/C]TCCACTAATCCATCA | 8816 |
rs560564734 | snp | G/T | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050820 | AGTTTTCAGCATAGC[G/T]TTCAATCAAGTTTCC | 8816 |
rs560596765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140547 | ACACTCCTCAGGAAA[A/G]ATTTCAACTCAGTGG | 8816 |
rs560600162 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093911 | TGCCCTTATAATGGT[A/C]CTAAACACAGGCCAC | 8816 |
rs560663730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115422 | GGAAGATAATCTTCT[G/T]TACTTAACTACTCCT | 8816 |
rs560676168 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050817 | TCTAGTTTTCAGCAT[A/T]GCTTTCAATCAAGTT | 8816 |
rs560683407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055960 | TAGTAGTTGGACATT[A/G]TAATAATAATCCTGG | 8816 |
rs560846585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113100 | ATGACTCTCCTCCTA[C/T]ACCTTCAGGCTACCA | 8816 |
rs560932457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112446 | TATGTGATTTAGTAA[C/G]AGAGGGAACTGGGTG | 8816 |
rs560961847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145152 | CCTCCTGTGTAGCTG[C/G]GACTAAAGGTGCACG | 8816 |
rs561009181 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153665 | CCCGAGGCGGGGGAA[C/T]CGGGAGGTAGGGCCG | 8816 |
rs561034818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072984 | AGATCATGGGTTCTG[C/T]GGCCTCTAAAAAAGC | 8816 |
rs561072022 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065355 | CCGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 8816 |
rs561138315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105819 | GCTTTCAGACTTGAA[C/T]TGACCACTCTACTGG | 8816 |
rs561151585 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102280 | TGCCCGGCTAATTTT[C/T]GTATTTTTAGTAGAG | 8816 |
rs561180893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088757 | GCTGTGGGTGTTCTC[A/G]GAGCACACAGGAATG | 8816 |
rs561198192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103382 | GGGGGCGTTAGCCTG[C/T]GGACAGTTTTAAAAG | 8816 |
rs561236953 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094519 | AAAGAGCAGCAGCCA[A/C]CAACACTGAAAACTT | 8816 |
rs561243724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096999 | AGTGCAGAAGGAGGG[A/G]GTGGGAGGATATGCA | 8816 |
rs561262062 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142762 | CATGTATAACTATAT[A/G]AGGAAAGACACCTAT | 8816 |
rs561265338 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151612 | CCCCCCTCCCCTGAG[A/C]CAGGTTTCGGGGAGC | 8816 |
rs561281803 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072288 | TAGAGAAAGGGACTA[C/T]TGTGCTTTTAAAAAA | 8816 |
rs561288562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152515 | AGGCATCAGGAGAGA[C/T]CACTTTGCACTTGGG | 8816 |
rs561289833 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072584 | GCCTGTGAATAGCCA[C/T]TGCACTCTAGCCTGG | 8816 |
rs561314273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129668 | GATCATTTCAGACCA[C/T]TTAAGCCAGCCCCAT | 8816 |
rs561315620 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086647 | AAAAAAAGCAAAGTT[A/T]TAACTTTAGAGGGCC | 8816 |
rs561368074 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099263 | TCAACACACACACAC[-/AC]ACACACACACACACA | 8816 |
rs561381407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095405 | CAAGGATTTGCTATA[A/G]AACACAAGAACAGGG | 8816 |
rs561432983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084885 | TTCAGTATGACCCTC[C/T]GGATGACCCTAAGGA | 8816 |
rs561477817 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132238 | TTTCCACAGTGGCTG[-/C]CCCATTTTATATTCT | 8816 |
rs561522744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120453 | TGATTCCAAATGATG[C/T]GAAAGTTTTAATCTT | 8816 |
rs561581002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110579 | AGTCCTTTTCACTTA[C/T]TTAATAGTGTCTTTG | 8816 |
rs561604596 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075456 | TTATATATTATAATA[C/T]AGAATAAATACAATA | 8816 |
rs561615460 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119704 | AGAGAGAGACTGTCT[C/G]AAAAAAAAAAAAAAA | 8816 |
rs561716048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127319 | GTGATAAAAAGAAAC[A/G]AAATATCAAGCAGTG | 8816 |
rs561796965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143736 | AATAAGTACTAAAAC[C/T]GAAAAGAACAAAAAC | 8816 |
rs561835194 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054463 | GCCTGGGCCATTGCT[A/G]GGAGTTCTAGGAGTC | 8816 |
rs561851287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135362 | TGCCTTGATGAAGCA[G/T]TAAAAATAATTGTAT | 8816 |
rs561957896 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151607 | TTCACCCCCCCTCCC[-/CT]GAGCCAGGTTTCGGG | 8816 |
rs562005954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126345 | TATTTTTAGTAGGGA[C/T]GGGGTTTCACCATGT | 8816 |
rs562025402 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095562 | AAGTACACACACACA[C/T]ACAAAAACCACTCAA | 8816 |
rs562028591 | snp | C/T | | | missense | DCAF5 | GRCh38.p7 | 14:69053945 | AGGCCACTGTGGCCA[C/T]GAACAGCCCTGCTAC | 8816 |
rs562037036 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052344 | GAAGCCTGGGGCAGT[A/G]AGGCCACACTAGTCA | 8816 |
rs562039605 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117349 | TTCTCTTATAGCCTG[A/T]ACCTAAATAATGAGC | 8816 |
rs562065126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091570 | CTGTTTCCCCTTAAT[C/T]GTTTCTACCTGACAT | 8816 |
rs562073747 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053478 | ATAGGTCCTTTCTGA[C/T]GGAGAACTAAAAGGA | 8816 |
rs562094342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147886 | TATTCTGCTAGCTCT[A/G]TAAGTTCCAATGCCT | 8816 |
rs562129998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116575 | TCAGGAATGTGAATA[C/T]AGGTCGGAGCACTCT | 8816 |
rs562162404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148509 | AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCG | 8816 |
rs562163266 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073331 | GAAGGTGGCCAAGGA[A/G]AGAGACATCGAGAGA | 8816 |
rs562191839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092449 | TAATGAGACTTTGTC[C/T]CTACAAAAAAATTAA | 8816 |
rs562219561 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154367 | AAAGATGGGCTGTAC[A/C]TCTCTGATCTGGGGA | 8816 |
rs562255898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101239 | AAGAACAGCATCAGA[A/C]TGCAATGCATCAGGG | 8816 |
rs562266912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094178 | CACCCATAGCAGCAG[A/G]GGTTTGCAGCAGCTC | 8816 |
rs562281799 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154978 | CCGCTTTAATACTTG[C/T]TGAATTCATGAATGT | 8816 |
rs562341829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109069 | AATACAGGCCAGGCG[C/T]GGTGGCTCACACCTG | 8816 |
rs562345067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114999 | CTATTCATTGCAATT[A/G]TAAGTAGGAGAGATA | 8816 |
rs562355110 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143553 | AAAAATCTGTTAAAC[-/T]TTTTTTTTTTTTTTT | 8816 |
rs562356174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124860 | ACTGCTTCTGCTACT[A/G]TATTTTTTTTTAATT | 8816 |
rs562363098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140832 | CTTAAAAGTGGCAGC[A/G]GAGGCCAGGAGCGGT | 8816 |
rs562379016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099924 | TCAAAGAATAAAATA[A/G]CATTAAAAAAAAAAG | 8816 |
rs562425571 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089318 | CAAAAAAGCCAAATA[C/T]AAATCTCTGTATTTT | 8816 |
rs562562815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058695 | ATCTGGACAACATGG[C/T]AAAACCCCGTCTCTA | 8816 |
rs562608733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088086 | CGGGCTAAAGCTGTA[A/C]AGAAGCTGGCCCATT | 8816 |
rs562614552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097987 | GCCAGAGGAGATGCT[G/T]AACCATGAATCTAAT | 8816 |
rs562617535 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087478 | TTAAACAAAAAAAGT[-/A]AAAAAAGTGTAAGCC | 8816 |
rs562633518 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147336 | TCCTGAAAGCCTTTT[G/T]TGACATTCAAGGGAA | 8816 |
rs562643533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088665 | GTTCATTCCTATTAC[A/G]GAAATTCTCAGATTC | 8816 |
rs562670918 | in-del | -/CATC | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132037 | TTTTGTTTATCTATT[-/CATC]CACTGATGGACCCTT | 8816 |
rs562672403 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144809 | TACAAAGGGAAAAGA[C/G]AGAAACAGCACCTGC | 8816 |
rs562704743 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056311 | CTGTTAGCTATAGGA[A/G]TAGGTAGGACACATG | 8816 |
rs562719236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124049 | TGTCTACTCTAGGAA[C/T]CTCGTATAAGTCAAA | 8816 |
rs562719266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113992 | CTCTGAAAACCGTAG[A/G]TTATCAAAGAAACTA | 8816 |
rs562727870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130933 | TTTTTATTGTAAAAT[G/T]GAGAAAATACCAACT | 8816 |
rs562804810 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123302 | ACCTTGTCAGTTTTG[G/T]TCACTGGGAAATACC | 8816 |
rs562841626 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069958 | ATAACAGTCGTTGAG[C/T]AGCTACTAAGTACTC | 8816 |
rs562843137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081480 | AGAGGGCAAGCTATT[C/T]ACTGATCTGAATGTT | 8816 |
rs562867614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138676 | GAGCAAATCATTTTA[C/T]CTCTTTGCTCCTTTG | 8816 |
rs562891302 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139553 | GCATGGTGCCTCATA[A/C/T]CTGTAATCCCAGTAC | 8816 |
rs562898522 | snp | G/T | 8.25212e-05 | 0.00642291 | missense | DCAF5 | GRCh38.p7 | 14:69055184 | GCATCCTCACACGTG[G/T]GTGTTGGTGGAGTTG | 8816 |
rs562903857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131618 | AGGTAAAATGACTTG[C/T]TAATAATCCAAAGAG | 8816 |
rs562987184 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081965 | ATTAGCTGTATTGAC[A/T]AGGACAGAAAAACCA | 8816 |
rs563000302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146788 | GATCAAATAATAAAA[A/T]ACCTTCACAGCAATG | 8816 |
rs563025831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058122 | GTCCTAATCCTTAGT[A/G]TTAATATATAAATTC | 8816 |
rs563027744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067121 | GCTAGAACATAAGCT[C/T]CATGACAGCAGGGCT | 8816 |
rs563061036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063384 | CAGAACACATGCACA[A/T]AAATTCTGATCAAGT | 8816 |
rs563131666 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095556 | TTTTTTAAGTACACA[A/C]ACACACACAAAAACC | 8816 |
rs563139510 | in-del | -/TATATATATATAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105932 | ATATATATATATATA[-/TATATATATATAT]ATCTCCTATTGGTTC | 8816 |
rs563149629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112348 | GTATGACAGGTCCAT[A/G]TTGGAAAAATTTGAA | 8816 |
rs563170352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087430 | TTACTGCCAGAGTCC[A/G]CACTATATTGCAAGA | 8816 |
rs563233122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055816 | TTTTAGAATCAGATG[A/T]GGGGAAATGCATGGT | 8816 |
rs563267470 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109217 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAACT | 8816 |
rs563272641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121524 | TAATAGCTTATATAA[G/T]TGGGTGAATGGTTGT | 8816 |
rs563282330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142163 | TAATTAGCTGGGCAC[A/G]ATGGTGCATGCCAGT | 8816 |
rs563318994 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114472 | CAGTGAGTATTACTA[C/T]GTGCTTCCTTCTGTC | 8816 |
rs563335795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120661 | GTAGCAGTAAAGATA[C/T]GGCCCAGGGCATCTT | 8816 |
rs563358708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151601 | GCCGTCTTCACCCCC[C/G]CTCCCCTGAGCCAGG | 8816 |
rs563387084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104249 | TCTCCACATCTTTAC[C/T]AGCATGGCTTGTATT | 8816 |
rs563408932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129598 | GGCAGAGATTTATTG[C/T]TTAGTTCCACAGAGA | 8816 |
rs563410581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072109 | AGCCCCATTTCCCTA[C/T]TTGGCTTTTAAGAGC | 8816 |
rs563429870 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153570 | GTTCGGGGAAAATGC[G/T]GCTGGAGTGGGGGAA | 8816 |
rs563550326 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131266 | CTTTTCTTTTCTTTT[C/T]TTTTAACTGTGAAGC | 8816 |
rs563573513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113068 | TCAGCTTATTTCAGG[A/G]CAGCAGTGGGACAAA | 8816 |
rs563617457 | snp | A/C/G | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152742 | TGCGGGGAGGCGCGG[A/C/G]GAGGGGAAGGGGGTT | 8816 |
rs563629410 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133556 | GGCAGGGAAGAGGCG[C/G]GGGTACAGGCAGGTC | 8816 |
rs563661502 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118453 | AACTTTCAGGTTAAA[A/G]AAAAGGTACTATTAA | 8816 |
rs563716148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144135 | TTCTATACTACAAAT[C/T]TCATTGCCTTTCTAC | 8816 |
rs563720967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136808 | CATAACAAAGACTTA[C/T]CCAGCCCAAAATGTC | 8816 |
rs563723277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101487 | CTCTACTGGGGAGAC[A/G]GGAGTGGGAGTAGTC | 8816 |
rs563760176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062321 | TACATAAATTGTTCT[A/G]GTTTCTTCTAATTAT | 8816 |
rs563768861 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050776 | CAATGACCATTGTCA[C/T]GGATGTGGAACACTG | 8816 |
rs563816223 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069044 | ATGTGCCTCACATGT[A/G]TTTATAACCAACTAC | 8816 |
rs563835816 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127699 | TAACAAATTTACCAC[C/T]CTGGTGGAAGATGTT | 8816 |
rs563874270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128801 | AAAACCAAAAACAGA[A/G]TATCTGCCAGGCCCA | 8816 |
rs563887245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143030 | GAAGGAGACTTTAGA[C/T]AACTGCAAACATCAG | 8816 |
rs563897011 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065053 | CCTGAAAATTCAGAC[C/T]ATGGAAAAACTGTTT | 8816 |
rs563929029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137533 | AACATAATAAAGCTT[C/T]CTTGTCTCTTCTTTG | 8816 |
rs563935475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085994 | TGCCGTTTCACACTA[A/C]TGTCGGCCTCAGTTT | 8816 |
rs563938418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118714 | GGCTCTGAGGCCAGA[G/T]AGCCTAAGTTCAGGT | 8816 |
rs563948105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135251 | CCACTGGTGCCTTGG[C/T]GCTAGGGCAGTGACG | 8816 |
rs563972124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086603 | AAGTGGGCTTAATCA[A/G]GCGTGCATGGAGTTA | 8816 |
rs563988054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061328 | TTGGCAGGAACATCA[A/C]CTATTCTTACTTAAA | 8816 |
rs564014066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078902 | GACAGAGTTTCTGCC[A/G]CCCAGGCTGGAGTGC | 8816 |
rs564036771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136151 | TACAGGGTCCTACTC[C/T]GTCACCCAGGCTGGA | 8816 |
rs564092203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067727 | CTGCAACCTTCACCT[C/T]CCCAGTTCAAGCGAT | 8816 |
rs564201590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077979 | ACTGGACTGGTGGCT[A/C]TGTAAGGCTCATTTA | 8816 |
rs564213644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084318 | CAGGCTGTCTGCTGG[A/G]CCATATGCAGAATAT | 8816 |
rs564225457 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061365 | TATCTCAGGGACCTC[A/C]AGAATTAATCATTTA | 8816 |
rs564254503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075920 | CAAAAGGCATGTTAG[C/T]TAAAACTCAGCAACG | 8816 |
rs564256250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067277 | AAAAATCTTCACATA[C/T]GGGCTCCATCACCCA | 8816 |
rs564268905 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134733 | TATGAGAAGTCATAA[C/T]ACACTTTTTAGATGA | 8816 |
rs564273918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058967 | ATATTTTCCTCTCCA[C/T]GCACAGTGAAGTTTA | 8816 |
rs564384364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069388 | AATCAGCCATTCCAG[A/G]TGGGTAGCAAGGAAG | 8816 |
rs564410955 | snp | C/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090824 | AACACTAAACATTAG[C/T]GAGAGACTAAGGTTT | 8816 |
rs564447558 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139476 | CTGCACTTTAGCCTG[A/G]CCCACAGAGCAAGAT | 8816 |
rs564511391 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154284 | TCAGTTTTGCCCTTT[C/G]AAGTTAGCAGGAATT | 8816 |
rs564562059 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097386 | CCTCAGAACAATAGC[G/T]TTAAAATTTTTTTAT | 8816 |
rs564607755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133432 | GAGAAATACAGACTC[A/G]AGATTGCCAGATCTC | 8816 |
rs564688854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137501 | TTTGCAAAATTCCTT[A/G]TATACACAAAATTAA | 8816 |
rs564697381 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113989 | GGGCTCTGAAAACCG[C/T]AGGTTATCAAAGAAA | 8816 |
rs564789934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059575 | GGGTCGAGACTCAGC[A/G]GCCTTTCAGGATAAC | 8816 |
rs564821229 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154844 | AAATGTGTAATTAAT[C/G]ATTTATTTTTGTGAT | 8816 |
rs564827657 | snp | A/T | 0.0150606 | 0.0854603 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154001 | AACTAACGATATATG[A/T]TATTTAATTGGGTTC | 8816 |
rs564828309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056978 | TCATAATCTTACCCT[A/G]GAGAGTTTCAAGGGA | 8816 |
rs564898607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137935 | ATGTATACATAAGAC[A/G]AAACATAGTATACAT | 8816 |
rs564927781 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105090 | GGTAGTTCCTCAAAA[A/G]GTTTAATATAGGATC | 8816 |
rs564962549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129824 | AGTGCCAGGCAAAGA[A/C]AAGCAGAGGCCAGGC | 8816 |
rs564962642 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138600 | CTTTCCCTATTGAGG[A/C/G]AAAAGGTCAGAAGAC | 8816 |
rs564969891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066294 | CGCACACCACCACGC[C/T]CAGCTAATTTTTTTG | 8816 |
rs565001087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088853 | TTCTGTCTAGACTCA[A/T]CAAAGAATATACATG | 8816 |
rs565006198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095524 | TCTCCTGTGGGGTTT[A/G]TTTTGTTTTGTTTTG | 8816 |
rs565017165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147058 | GCTTTTAGACTAATT[C/T]ATCTACAAAAAACTG | 8816 |
rs565039494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082381 | GCTTCTTTGAGCCAT[C/T]TGCCATTTCAGCTCC | 8816 |
rs565082125 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139996 | ACAGAGAGGCCAGGC[A/C/G]CAGTGGCTCACACTT | 8816 |
rs565095069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078298 | AAGATGTTCAACATC[A/T]CTGATCATTAGGGAA | 8816 |
rs565159846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082656 | ATTAGCCCCCCTCCA[C/T]GGGCTTCAGTTTTTG | 8816 |
rs565216828 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152696 | CAGGAGGAGGGTGAC[A/G]GGGGAGAGCGAGAGG | 8816 |
rs565228762 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142926 | TTGATAACTAGAGTA[C/T]ACCTACTCCTAATCA | 8816 |
rs565230140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147775 | TTGCTCATGCTATTT[C/G]AAAAACTTCTAAAGG | 8816 |
rs565274061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130709 | TTTCTAAAATATAAC[A/G]TATTAGTGACTGTAT | 8816 |
rs565280060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145232 | TATGTTAACCAGGCT[G/T]ATCTCAAACTCCGGG | 8816 |
rs565308781 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069786 | GCAGCAGTTAGTTTT[-/A]AAAAAAAAAGTTTGT | 8816 |
rs565333182 | snp | C/T | 3.303e-05 | 0.00406373 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122326 | GTGGATGGCTTGTTC[C/T]ATGTGCCATAGCAGA | 8816 |
rs565347313 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113223 | CAGGGTGAGACCTTC[A/T]TCACTGCTCCAAGGA | 8816 |
rs565353945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101835 | ACAATGGGTAAGTAT[C/T]TGTGTATCTAAACAT | 8816 |
rs565422060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069531 | CCTCAAATTCCTGGG[C/G]TCAAGCAATAGTCCT | 8816 |
rs565501310 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053814 | CAATTTTTTTTTTTT[G/T]GTAAGGCTACTTTTG | 8816 |
rs565552301 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086998 | GCAAGATGTAGGGAC[-/TAT]TAGACCAGGCATCAT | 8816 |
rs565593449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073167 | AGTACAGCAGAGGAA[C/T]TGACATAACTATTTT | 8816 |
rs565661938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061810 | GTTGCAGCATACAAG[A/G]TAGTGTCTAGAAGAC | 8816 |
rs565671794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119086 | AGAACAGCTGGTTTC[A/C]TGTTGTTTTTTTCAA | 8816 |
rs565689694 | in-del | -/CT | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107638 | CACCAGAATACCTGG[-/CT]CTCTGCCACATAACT | 8816 |
rs565730439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093871 | GTATCCCTGCAGGCC[C/G]CAAGTAGTAATCCCT | 8816 |
rs565744084 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060757 | GGCTGGTCTCGAACA[C/T]CTAACCTCAGCTGAT | 8816 |
rs565753150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087474 | TTGCTTTAAACAAAA[A/G]AAGTAAAAAAGTGTA | 8816 |
rs565823169 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100530 | GAGGGCAAATAATAT[C/G]CCTCCTTTGGTAGAT | 8816 |
rs565833924 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051585 | TCAAGTTAACCAGAA[G/T]AAACTCTGATTTCTC | 8816 |
rs565904729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149314 | AGTATCACAGCGATG[C/T]CCCTTTCTGGTCATA | 8816 |
rs565979706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078129 | AGGAAACTCATAAGG[C/T]CAGTCTTGTTAAACT | 8816 |
rs566094984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083981 | AATGGGTTTTACAAA[C/T]GTGACTGAAATTCAG | 8816 |
rs566134439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099362 | ACATTTGTCTACCCA[A/T]GAAACCTGATCTCGA | 8816 |
rs566181000 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117496 | CTAAAGGCCACGGTG[C/G]GTATGGCAGTGGCAC | 8816 |
rs566225556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126812 | ACAATGGAGCAAAAA[C/T]GGTCTTTTCAACAAA | 8816 |
rs566248326 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059192 | TGGGCCCAAGTGATC[A/G]TCCCACCTCAGCCTC | 8816 |
rs566248435 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69092581 | CATGGTCACGCCACT[A/G]CACTCCAGCCTGGGT | 8816 |
rs566276237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132404 | AATAACTCTCAAGTC[A/C]TTTTAAATATCTCAG | 8816 |
rs566285524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69117847 | AATAATCAAGAATAG[C/T]TACATGTCAGCACCA | 8816 |
rs566292491 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050655 | CAGTTCCAGAGTCTC[A/G]CTATCTTAAGTCCCT | 8816 |
rs566358655 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063034 | AACCAAAACCACTGG[C/G]GGAAATAATAGAGAG | 8816 |
rs566362972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142645 | ATGACTTACTAGCAC[A/T]CTCTGAGCAAATCAG | 8816 |
rs566439704 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122004 | AAATAAAGAAAAAGA[C/T]AGGTGAAGAAAAGCA | 8816 |
rs566490422 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144545 | CCACGCCACTGCACT[C/G]CAGCCGGGGCGACAG | 8816 |
rs566507136 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109527 | ACTATTCTGACTTCC[-/A]ATAACTTGCCTGTTC | 8816 |
rs566507956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059822 | TTCAAAGGGCTAAAT[C/G]TGCCTCCTGGTGGAA | 8816 |
rs566544045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116667 | ACTTACAAGGTCCCC[A/G]TGAGTCCTATACATA | 8816 |
rs566544707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082632 | GAGCAAGATGAGGGG[C/T]CATTAACCATTAGCC | 8816 |
rs566554362 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053046 | TAGGATCTAGCACCT[A/G]ACTGGTTAAAGTCTG | 8816 |
rs566580755 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083219 | CATAAACACTTTATT[A/G]TTATATGGAAAACAA | 8816 |
rs566581167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074757 | TCCAGGTGTGGGCTG[A/G]GTGCGGTGGCTCACA | 8816 |
rs566650878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107512 | AGGTGATTCTGATGC[C/T]CCTTAAAGTTTGAGA | 8816 |
rs566672014 | in-del | -/AGGATACT | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068850 | TAAAGAGGACCATCA[-/AGGATACT]AGGATACTGACAATA | 8816 |
rs566677628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067916 | CTGGGATTACAGTCC[C/T]GAGCCACTGCACCTG | 8816 |
rs566685491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125687 | TCAGGAATGGAAAAA[C/T]TCCACTGGAATATAA | 8816 |
rs566783710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059274 | ATTTTTCATAGAGAT[A/G]GGGTTTCCCTGTGTT | 8816 |
rs566791965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | DCAF5 | GRCh38.p7 | 14:69115672 | CTGCTACTCACCCCC[A/G]TTCCCACATCCTTTA | 8816 |
rs566818693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057288 | GAGATGTCTAAGGGA[A/T]TAAAAGAGCTTGGTG | 8816 |
rs566963862 | snp | A/G | | | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116438 | AACAACCTGGGCTCC[A/G]CAGGGTTAAACATGA | 8816 |
rs566986848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122600 | AAAATGAAAGGGATA[A/G]GCACTGATATTGAGA | 8816 |
rs567008609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096477 | AAAGGCTTGACTAAA[G/T]TTCTGTAAAGAAATC | 8816 |
rs567047109 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153993 | TGATTTGAAACTAAC[C/G]ATATATGTTATTTAA | 8816 |
rs567071159 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128671 | ACTGGGGAGGATGAG[-/TT]GCAGGAGAATCACTT | 8816 |
rs567148392 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094998 | AGAGAAAAAAGAAAT[G/T]ATCAAAGTCAATGAA | 8816 |
rs567165794 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154401 | TAATAATAATTTTTT[A/T]TAAAAAAAAAGATCG | 8816 |
rs567172959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072674 | AAAAAATGTGGGTGG[A/G]ATCTGTAAGAATAGT | 8816 |
rs567227115 | snp | A/G | 3.33244e-05 | 0.0040818 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152880 | CAGGCGTCTCCTCTG[A/G]AAGTCCTGAGTGAGC | 8816 |
rs567233778 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142446 | TTTTACCCATTCAGT[A/G]AATGGCCATGAAAGT | 8816 |
rs567245146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144946 | ATCCTTCCATTTCTC[C/T]GATCCCATGCAGAAA | 8816 |
rs567262495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151974 | TGCAACAGCGGCCGC[A/G]GGAAACGGGGTGCGG | 8816 |
rs567265570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104390 | TACCCATTTAAAAAA[A/C]TCAAACCTGAATTTG | 8816 |
rs567307259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130133 | TTAACATTCTTCTTA[C/T]TTTATTGCTCAGAAA | 8816 |
rs567326419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103674 | AAACTCGCTTGTATA[A/G]CTTGTATATGTACAT | 8816 |
rs567368430 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121935 | AATATGTGTGTGTGT[C/G]TGTGTGTGTTTCTGT | 8816 |
rs567399723 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124220 | TATTTTGTTTATCCA[A/C]TAATCCATCAATGAC | 8816 |
rs567406436 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143550 | TTTAAAAAATCTGTT[A/G]AACTTTTTTTTTTTT | 8816 |
rs567474644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131054 | TGTCCTTGTGTCCGT[A/G]AAGTATCATCCATGA | 8816 |
rs567553672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145558 | TAGCAACATAAGAAA[A/T]TCAAAAAATTTAAAG | 8816 |
rs567558066 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076374 | TCACAATAGCCAAAA[A/G]GTGGAAACAACCCAA | 8816 |
rs567595921 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074358 | ACATGAAGACACTAT[C/T]ATCAAAAATGAAGAA | 8816 |
rs567637358 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128670 | CTACTGGGGAGGATG[-/A]GGCAGGAGAATCACT | 8816 |
rs567709410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117670 | GAGTCAAAGGGCACA[C/T]TCAGAGGAGGCACTC | 8816 |
rs567732127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085179 | AAACAGATCTTTAAT[C/G]TTTAATAACTTAAAT | 8816 |
rs567733794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150958 | CTTACAATTCCGTTA[A/G]CATGATTAGTTCAGT | 8816 |
rs567767538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086111 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 8816 |
rs567773350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078285 | CTAAGCACACAAAAA[A/G]ATGTTCAACATCACT | 8816 |
rs567807452 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099636 | AAGTATCTTAATTAT[A/G]TCTTAGACTTTAAAG | 8816 |
rs567841596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110414 | GGGATTACAGGCACA[C/T]AACACCACGCCCCAC | 8816 |
rs567865352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111133 | TTGACATTAAGCCCC[G/T]GGGCTTTATTTTCCT | 8816 |
rs567884897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062950 | ATGTACAAAAAACAT[C/T]TCTAATCCATTTGCC | 8816 |
rs567886446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150055 | TGTTAACACAGCTGT[A/G]TACTCATAATGGAAG | 8816 |
rs567968919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071601 | AGAGAAAGAGGGAGG[A/G]AGGGAGGGGGAAGAG | 8816 |
rs567978811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128920 | CTCAGGAGTTGGAGA[A/C]CAGCCTGGGCAACAT | 8816 |
rs567989912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120122 | AGGATCCTGCTCTGT[C/T]GTCCAGGCTGGAGTG | 8816 |
rs568046236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077164 | CTGTCTTTTGCCCCC[A/T]TCTGCTCATTTCCCT | 8816 |
rs568093592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126630 | TGAAGAACAAAGTTG[A/G]AGGACTGACATTACC | 8816 |
rs568129371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068133 | TTTTACATCGAGTGC[A/G]TATGTCTGTGTGTGT | 8816 |
rs568195430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092786 | TGCAGAGCAAGCAGT[A/G]CAACAATTAGAAAAG | 8816 |
rs568220510 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122970 | CCCATTTTTACTTTT[A/T]ACTTTTACTTTTTTT | 8816 |
rs568356242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061538 | TGAGTTCATTCAGCC[A/G]ATGTGCAAATGATCC | 8816 |
rs568363023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084398 | GATCGTATCTTGGAT[A/G]TTGAGTTTGAAGAGG | 8816 |
rs568398419 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099174 | AAAGAATCGCTTGAA[C/T]CTGGGAGGCGGAGGT | 8816 |
rs568408081 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062316 | GGTCCTACATAAATT[A/G]TTCTAGTTTCTTCTA | 8816 |
rs568472980 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141329 | ACCATATAACTTATC[A/C]TTTAAACTGGGACCT | 8816 |
rs568500747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107356 | TCTGATTAACCACTG[C/T]TTCCATCTTGTAAGA | 8816 |
rs568523279 | snp | G/T | 0.000199428 | 0.00998371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062554 | AGATGATGAAATGAA[G/T]GAAAGTAAATAGGTT | 8816 |
rs568576893 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134763 | ATGCCAATATTCTGA[A/C]TGAATTGGTTAAGAC | 8816 |
rs568608443 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135757 | CCCAATACACAGAGG[C/T]TTTTCTGATGAGACT | 8816 |
rs568648115 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088650 | GCTTTTCTCATCCAT[A/G]TTCATTCCTATTACG | 8816 |
rs568649166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147163 | ATATAGGTGTAATAA[C/T]AGCTATTATTCAATG | 8816 |
rs568657410 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153747 | CCCTCTCCCGGTAAA[A/T]GTTTAACACCACCGC | 8816 |
rs568669231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058467 | AAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 8816 |
rs568715481 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131251 | TTGCTAAAGTGTTTT[A/C]TTTTCTTTTCTTTTT | 8816 |
rs568748251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141021 | CACCTCTAATCCCAA[C/T]GGGATTACAGGCTGA | 8816 |
rs568795233 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121804 | TTCAAACAGGAGCCA[G/T]CTGTGGGTCAGGACA | 8816 |
rs568806205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073784 | GAGAAGAAGGATTAT[C/T]CACATTCTATTTTTA | 8816 |
rs568811492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142070 | AAGGCCAAGGTGAGA[A/G]GATCACTTGGGCCCA | 8816 |
rs568902323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139354 | CTGGACGTGGTGATG[C/T]ACACATAGGTGTACA | 8816 |
rs568921600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082502 | GCAGCCAATAACAGT[A/C]AAATAATCAGCAGAA | 8816 |
rs568928922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143336 | CATTCAGACCCAACC[C/T]GGAAATCTAGCTCCA | 8816 |
rs568979022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106562 | GAATACTTTTGTAGA[C/G]ATAGGGTGTATGTTG | 8816 |
rs568983514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089029 | AGTAGATTAGTTCCA[C/G]TATAAATCCATTATT | 8816 |
rs569037232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121160 | GTCAGGCCAGACAGA[C/T]AGATTGGGATTTAGA | 8816 |
rs569064001 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114490 | GCTTCCTTCTGTCTC[A/C]ATTTTTTTAAAGGAT | 8816 |
rs569064119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124564 | TGATGTCTTAAGTGT[A/G]GCCCACAGTGTTCTC | 8816 |
rs569076254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115458 | CTGAGGCCCGTGAAA[C/T]AAATTATAACATCAC | 8816 |
rs569079007 | snp | A/G | 0.000131928 | 0.00812076 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075320 | GCCAGCAATAGCAGT[A/G]CATTCATGTGAAGGA | 8816 |
rs569154220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066949 | CAATGTGGTCAAGAT[A/T]TCTTGATGTCTTGGT | 8816 |
rs569163731 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140536 | CTTTTAGTTAAACAC[G/T]CCTCAGGAAAAATTT | 8816 |
rs569211615 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153110 | AGCCATGGCAGGCAG[A/C]GCGAGGTGTGCAGAC | 8816 |
rs569359371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129921 | ACAACTACATACTCT[A/G]GTTTTGGTTTTTTGG | 8816 |
rs569378982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063787 | CCTCCTTATTGCCAC[A/G]TACATATCTTTTTTA | 8816 |
rs569390821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062852 | GAAAAGGCCAACCAT[A/G]AGCAAAATGAGACTG | 8816 |
rs569513771 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076224 | ACTGCTGTGGAAAAC[A/T]ATATGGCAATTCTTC | 8816 |
rs569550325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103024 | GCTACATTACCAGGT[C/G]ACAGGAATTTTTCAG | 8816 |
rs569588027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094913 | GATACAGGTAGCTTT[C/T]AAACCACACTGTGAG | 8816 |
rs569589675 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057066 | CCTCAGTCCCACTCT[G/T]AGAGGTTCTGATTCA | 8816 |
rs569611763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110221 | TATTCTTAATGTATG[C/T]ATTATGCTTTTTTTT | 8816 |
rs569625249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086782 | ATTTATCCAAGGCCA[C/T]TTTGTTGGATTCATA | 8816 |
rs569667542 | snp | A/G | 0.000399281 | 0.0141238 | missense | DCAF5 | GRCh38.p7 | 14:69054545 | CTCTGGGCCATTGCT[A/G]TGTTTAGACAGGCTT | 8816 |
rs569795771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149371 | GTTAAAGTATCTTAA[A/C]GTGTCAAATAACCAT | 8816 |
rs569797283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079918 | AGCGCATATAGGGAG[C/T]GCTGGGGGTTGGGGT | 8816 |
rs569844835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138033 | GGGGGGACTACTGTA[C/T]GTCTAAGGCAAAGCA | 8816 |
rs569857144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149923 | GACACTAGTTTTAAA[A/C]GTGGGAAAATTATTG | 8816 |
rs569878623 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100148 | GATATATGGATATCA[A/G]TAGGAAGATACATTA | 8816 |
rs569880761 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133047 | TAATTATTATGCTAT[C/T]TGAACTCAAACAACA | 8816 |
rs569898771 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065347 | TGATCCACCCGCCTC[C/G]GCCTCCCAAAGTGCT | 8816 |
rs569902442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143422 | TCATATGTAATATAA[A/G]GATAATAATACTACC | 8816 |
rs569908973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144307 | GCCAGGCGCGGTGGC[C/T]CACGCCTGTAATCAC | 8816 |
rs569910726 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116875 | GTTATTATGCTTTTA[A/T]TCCAATTGTATTAGT | 8816 |
rs569917817 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083463 | CCTCAAACTGCGGCA[A/G]TGGAACCTAAAGTTG | 8816 |
rs569921926 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102954 | AGCACAGTATGTTTG[C/T]TTACACCAACGTCAC | 8816 |
rs569941839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151792 | GGCCTCCCCGGGAGC[A/C]ATAGGCTATCGATTC | 8816 |
rs569958680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061850 | TTCAAAGCCTAGTGA[C/T]TAGTTTAAAAAAATG | 8816 |
rs569972130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098950 | ACACTGACTTAAAAC[A/G]TTTTTAAAACAAAAC | 8816 |
rs569977991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085099 | TTCAAAAGAACTACT[G/T]TTTTCATAAGTCAGC | 8816 |
rs569985596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134896 | TCGAATGTATCTTAA[A/G]AATATAAAAAATATT | 8816 |
rs569992968 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135484 | CCTATTTTGTGAAAA[A/C]GTATCTATGAGATAG | 8816 |
rs570003230 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144910 | TGTCTAGATCTCAGC[A/T]CCCTTTCCTGTAAAA | 8816 |
rs570018226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069652 | TTTCTTTTTATTATT[A/G]TTATTAGAGACACAG | 8816 |
rs570055827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092720 | TCACAAAGAATTTTT[A/G]TATTCTATATAGCAT | 8816 |
rs570060467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077663 | GATTATAGGAATAGG[C/T]TACACGCCTAGCCAG | 8816 |
rs570101447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125816 | ATAAAAGCAAGTTTC[A/G]AAAGGATATGAAAGG | 8816 |
rs570116141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092043 | ATGAGGGTAGCAACG[C/G]TTCCTTCGTTACTTT | 8816 |
rs570220412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078208 | ATGATTTTAAAAATG[C/G]GCCAAGGACTTGAAC | 8816 |
rs570237854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124906 | TATACTTATGTCTCT[A/G]GCAAAAGCAAAAAGT | 8816 |
rs570241516 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125269 | CATAAATGTTAAGTA[A/G]GAATAAAGGGAGCCC | 8816 |
rs570251759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128291 | TCCCAGGTTCAACTG[A/C]TTATCCTGCCTCGGC | 8816 |
rs570254442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109573 | ATGGAATCACAGAGA[C/T]TCTTTTGTATTTGAA | 8816 |
rs570264353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120037 | TTAAAAATGTTTCTT[C/T]CTTTCTTTCTTTTGA | 8816 |
rs570427746 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116748 | ATATAGCAGCTATCA[C/G]ATCTTGACACAAAAC | 8816 |
rs570442178 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122119 | GTAATTCCACAGCTC[A/T]ATGAAATACAGGAAG | 8816 |
rs570459400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076280 | ATGATGCAGCAATTA[C/T]AATCCTAGGTATATA | 8816 |
rs570495190 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075563 | CTCGGCTCACTGCAA[C/T]CTCCGACTCCTGGGC | 8816 |
rs570504050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067998 | AGAGAAATAAAGGGG[C/T]TGAAATCCTATCTAT | 8816 |
rs570506411 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052566 | ACCGAGTGACTGCAA[C/T]GCTGAAAATCTGTTG | 8816 |
rs570524753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097443 | ATCCTCGTACACCCA[C/T]ATTAATTTAGCATAA | 8816 |
rs570529934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108726 | CTTGCATGAGTACTG[C/T]AAACCTATGTATGGT | 8816 |
rs570567354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067651 | AATCCAGCCCAGATA[C/T]TCTTTTTTTTTTAAG | 8816 |
rs570596813 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057695 | GAGTAATGGAGTGAA[-/AC]ACAGGATTAAGAGGC | 8816 |
rs570623807 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074342 | GTAACACTCATTGAG[A/C]ACATGAAGACACTAT | 8816 |
rs570674030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100297 | CTCCCTCTTTTAAAA[A/C]GGGTCCATGGAAGAA | 8816 |
rs570698995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089643 | TACCTAGGACTATCA[A/C]AAAATACCTTCTGTG | 8816 |
rs570725841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133114 | ATCCTAAGGGTCTTA[C/T]ATGTAGTGGCTCTTC | 8816 |
rs570772119 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107274 | AGGAATGGACGCAAG[A/C]AATCTCTGGCCTAAA | 8816 |
rs570773883 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060644 | TCAAGTGATCCTCCT[A/G]CCTCAGCCTCCTGAG | 8816 |
rs570812379 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077926 | GGGCACAGTGGAAAA[A/C]GCAGTGGGCTCAGTT | 8816 |
rs570826973 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154457 | TCAAACAAAATTATT[C/T]ACTTCTACTTTTTGT | 8816 |
rs570833648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057565 | AGTTCCAGTGTATTA[C/T]TACCCAGCTCCTACA | 8816 |
rs570873105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063831 | TTCCAGACTGCACCC[A/G]TCTACTCACTCAGCC | 8816 |
rs570940068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058297 | GCCGTGGCGGGTAGA[C/T]CACTTGAGGTCAGGA | 8816 |
rs570960686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114385 | GTCATTAAAAGAAGG[A/G]GCTAGATCTGTTAGT | 8816 |
rs570977082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140963 | ACACGGTGAAACCCC[A/G]TCTTTACTAAAAGTA | 8816 |
rs570981662 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078475 | CAAAAGCACTGAAAA[C/G]AAGATCAGAGATACT | 8816 |
rs570988488 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153038 | GGCCTCACGCGCGGC[C/T]GCTGCTCCCCCCACC | 8816 |
rs570996587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103884 | TTCTTTTGAGATTGG[C/T]TTTTTTTCAGTCAAC | 8816 |
rs571037670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147434 | AATGTTATTTCATTC[A/G]ATCCTTACCACAACC | 8816 |
rs571043729 | in-del | -/AGC | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154290 | TTGCCCTTTCAAGTT[-/AGC]AGGAATTACATCCTC | 8816 |
rs571055544 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116702 | GGTAAACACATTTAA[-/C]CACATTTTAAGCTAT | 8816 |
rs571110224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138359 | AGTACGGAAGTATAG[C/T]TCAGCAGGCTAAGAA | 8816 |
rs571122997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122078 | AATACTGCTGTAATG[C/T]AGAAAAGACAAGCTA | 8816 |
rs571144635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087633 | TATTTGTAGCCAAAA[C/G]GGGGGAAGACAGATT | 8816 |
rs571158905 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113435 | TTCTACCATCCCTAG[-/A]AAAAAATATGACATG | 8816 |
rs571165102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148136 | ACTTTAAACAAACAT[A/T]TAAAGGACCCCATTC | 8816 |
rs571180819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081026 | TACTAAAAAAAGGCA[A/G]TAACAAATGTAAGAG | 8816 |
rs571194997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146383 | ATAGGTATCAATTAG[C/T]TGACTAAAGAACCAA | 8816 |
rs571195568 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148271 | ACTACTGTAACCTCA[C/T]TGATGTTGTTAGGAT | 8816 |
rs571231064 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086118 | TCCCAGCACTTTGGG[A/G]GGCTGAGGTGGGTGG | 8816 |
rs571252258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088232 | GTACAGTGAAAAGGG[A/G]TCTCTATTGAGAGCC | 8816 |
rs571269355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129150 | AAATGCCTTGGGATC[A/G]TTTTAAATGATGTGT | 8816 |
rs571295865 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145710 | AATTGAAAACAGAAC[G/T]GATTCCTTCTTAACT | 8816 |
rs571365792 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109928 | TTGTACCAATTTGTA[C/T]TCACCTAAAATGTAT | 8816 |
rs571377594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113622 | AGGTTGGGGTTTCTA[C/G]GCAGCTGTGCTCAAG | 8816 |
rs571457229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137236 | AAATAGAGCTGGGGG[A/G]CACTAAAAACGGGTT | 8816 |
rs571491679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123694 | TCCCAGTGCCTAGTC[A/T]CTGTTCTTTTTTTTT | 8816 |
rs571575394 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136266 | GACTACAGGTGCACA[A/T]CACCATGCCTGGCTA | 8816 |
rs571697484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144700 | GATATAATTTATCAT[G/T]TAAGAGAAGCAACCA | 8816 |
rs571716809 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067181 | AACTGTGCCTAGCAC[A/G]TAGTAAGGTTTTTAA | 8816 |
rs571733058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079080 | GAATTCCTGCTACCC[C/T]GCCCCCCATACCACT | 8816 |
rs571762637 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056157 | ATTCCTATTTTTAAC[A/T]AATGGGAATTGCTCA | 8816 |
rs571809390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112696 | GAATAATAGAAGCTA[C/T]CTCATAGGGTTATCA | 8816 |
rs571882882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111398 | CCGTCTTATAAGATA[A/T]GTCTTTATAGGGATT | 8816 |
rs571883832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135774 | TTTCTGATGAGACTG[A/G]TGGCAATGTCAACAA | 8816 |
rs571883877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127224 | TTACAATTGCCAAAA[A/C]TTAGAAGCAACCAAG | 8816 |
rs571933313 | in-del | -/TTGA | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090203 | AAGAGAGGGAGAGAC[-/TTGA]TTGTCATTTCCACAG | 8816 |
rs571982887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091468 | TCGTGGCCAGCCTTG[C/G]TTTATGGTGTGTGCC | 8816 |
rs571983658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064918 | AGAAGACAGCTGGAA[A/G]GTCTCATATAAAGAA | 8816 |
rs572018702 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146472 | CTTTATAATTTATCA[C/T]AGCAAAGTTCCTCAG | 8816 |
rs572022199 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052234 | TTTATAAATAACCCC[C/T]CCACCCCCAGTGCCT | 8816 |
rs572045382 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094688 | GGTTTGCCGGGAAGG[C/T]AAAGCTTGGAAGCAG | 8816 |
rs572085502 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066910 | CTCCAAGAATGAGTA[C/T]GTTTTTGACTCAAAA | 8816 |
rs572101021 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112814 | TATGAGACACTGAGA[A/G]GTGAAGTAACTTATT | 8816 |
rs572163073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083012 | CTAAGAACAATCCAG[G/T]TCACCTTGTGTTCCT | 8816 |
rs572257964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077889 | GATGAAGAAAATGCT[A/G]TCTATAGGGATTAGG | 8816 |
rs572296789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069348 | TACTGATGAGTCAAG[A/G]GCAGCCTTCATGCAA | 8816 |
rs572341947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083524 | ACTCAAAATACAGAT[A/G]TGTCTGAAGAAACAA | 8816 |
rs572405226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089865 | CCATCTTATAATGCA[C/T]AGGACAGCTCCACAC | 8816 |
rs572408368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068245 | GAGCTTTACATGATG[C/T]CTTATCTAAGGATAC | 8816 |
rs572444172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133317 | AGGCCAGGCAGCAAA[A/G]TAAATGAGTCAGACT | 8816 |
rs572491359 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155392 | ATCTAGGACTTTGCT[A/G]GAAACTTCCTTAACT | 8816 |
rs572569957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140627 | AACAACCCATAGGAA[A/G]ACTGTAAAAACAAAA | 8816 |
rs572588971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131408 | TCCAAGAAACTGCAG[C/T]GCATTACAGAGGCAC | 8816 |
rs572662368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067702 | AGTGCAGTGGCGTGA[G/T]CTCGGCTCACTGCAA | 8816 |
rs572698835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059465 | GGAAAGTGACATTTA[C/T]TAAAATAGGAGTTAG | 8816 |
rs572754474 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128607 | ACAGTCTCTCCTGAA[C/T]TGAAGCAGCTTAAGT | 8816 |
rs572764460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133974 | AATACTAACCCTAGA[A/C]AATGTCTCTAATTCC | 8816 |
rs572798793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067016 | CTCAATACCACTTCC[C/T]GTCTTCCTCTGTTCT | 8816 |
rs572815693 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113202 | AGCCAGGAAGGAGAA[A/G]GTGTTCAGGGTGAGA | 8816 |
rs572836123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113885 | GCAAAAACATCCTAG[C/T]CCCCATGGCACTATG | 8816 |
rs572878966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105833 | ACTGACCACTCTACT[A/G]GCTTTTCCCATTCTT | 8816 |
rs572881621 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104772 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 8816 |
rs572902234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151106 | GGGAAACTGGGAGCT[A/G]GGTCTATAAAGAAGA | 8816 |
rs572924757 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121040 | GACAATTAAGGTGGA[A/G]GAACACCATGAACAA | 8816 |
rs572968660 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087089 | GCTTGCTAGACTGAA[A/C]GACTTGCTTACCAGA | 8816 |
rs572972169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097731 | AGCTGGGATTACAGG[C/T]GGGCACCACTATGCC | 8816 |
rs572987882 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155371 | TCTGGTCACATGCCA[A/G]CCCAAATCTAGGACT | 8816 |
rs573011739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089251 | TGTGTGCCAGGATTT[A/G]GAGACAAGACAATGA | 8816 |
rs573040896 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058492 | CCACTGCACTCCAGC[C/T]TGGGTGACAAGAGCG | 8816 |
rs573042177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103967 | ATCACTGAGTAGCAG[C/T]CTGTGGTATGAATGT | 8816 |
rs573076534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139387 | ACCTATGTGTCCTAG[A/C]TACTTGGGAGGCTGA | 8816 |
rs573090481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098676 | ATCACGAGGTCAGGA[G/T]ATCAAGACCATCCTT | 8816 |
rs573113357 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154618 | ATAAATTTTTAAAAG[A/G]AAGAAATCAAATTCC | 8816 |
rs573119392 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105173 | AAAACAGGTTCTCAA[A/C]AAAAATTTGTTCACG | 8816 |
rs573133637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095437 | AGGAGGTGATCCAAG[G/T]TGATCCAAAAGACCT | 8816 |
rs573135995 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144445 | GGCGTGGTGGCGGGT[A/G]CCTGTAGTCCCAACT | 8816 |
rs573196094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145976 | CTACTTCTTAACTTG[A/G]AATTAAGAGAGTAGT | 8816 |
rs573198178 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077952 | CAGTTTCTTTATCTG[-/C]AAAATGAGAGAACTG | 8816 |
rs573207654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095880 | GAAAGCTCTATAAGA[C/T]CGGTGGAATGCTTGG | 8816 |
rs573212546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138554 | TAACACTTTACTTGA[A/G]CAAGTCCTTTTTAAA | 8816 |
rs573216077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106730 | TTAAGAAGAAAACGT[C/T]AACATTTGATTTTAA | 8816 |
rs573220046 | snp | G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153308 | GCCCCTCCCCTCCGC[G/T]GGGGGCTGGCCGGAA | 8816 |
rs573277996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152527 | AGATCACTTTGCACT[C/T]GGGATAAAGCGAATT | 8816 |
rs573331274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130438 | GGAAAAGAGGAATGG[C/T]GAGTCATAGTTTAAT | 8816 |
rs573356082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085775 | GTCTGCCCCCTTCCT[C/T]AAAAAAAGTTTCCTA | 8816 |
rs573465412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146651 | TACAAATGAGAACTG[A/C]ACACTCCTAAAACAC | 8816 |
rs573503173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073002 | CCTCTAAAAAAGCTT[A/C]TGTGACACTGGGTGT | 8816 |
rs573520805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112039 | ATATGAGAATAAAGG[A/T]CCGACAATATCAGAT | 8816 |
rs573563732 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107439 | AAGGTCCCACCCCAA[A/T]CCAACAACTCAATCT | 8816 |
rs573639350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094080 | TCAGTATGGAGTGTG[C/T]AAATAAACCAGCATT | 8816 |
rs573679985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151231 | TCAGAGGATGATCTA[A/G]GGCCAAAATCTACCT | 8816 |
rs573791526 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101887 | CAGTATAAAAGATTT[A/T]AAAAAATGGTACACC | 8816 |
rs573792181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144329 | TGTAATCACAGCACT[C/T]TGGGAGGCCGAGGTG | 8816 |
rs573829470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063849 | TACTCACTCAGCCAG[C/G]TTTAGGTGCTCAATC | 8816 |
rs573889187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072009 | GCCAATTGACATTGA[C/T]CCAAAGAGGTTTTAG | 8816 |
rs573898598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120458 | CCAAATGATGTGAAA[A/G]TTTTAATCTTGTATT | 8816 |
rs573921683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129466 | GGGCGCTAAACAGCT[A/G]TGCCCAAGCCTCTGA | 8816 |
rs573998491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061123 | AATCCCTCAGCCTTA[C/G]CCTCCCAAGTAGCTA | 8816 |
rs574031883 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148589 | AATCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA | 8816 |
rs574040649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118379 | TCTTTTCCATTTCTA[C/G]AAGAAAGTCAACCTA | 8816 |
rs574063783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069136 | GGCCTAAGTCACTGA[C/G]AGTGAATACATGTCT | 8816 |
rs574094694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127152 | ATTTAACCAAAGGAG[C/T]TGAAACTTGTATCTA | 8816 |
rs574101917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119488 | TTATCCAGTGGATGA[C/T]GTAAAAAAAAAAAAC | 8816 |
rs574103875 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129678 | GACCATTTAAGCCAG[C/T]CCCATGGGCCTGGCA | 8816 |
rs574110666 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093519 | GAAGGAAGATAACAC[A/C/G]TTTTCTTTTTTTGCC | 8816 |
rs574121256 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135056 | TAAATTCTGATGTAG[A/G]CACTTGAAAGGATAC | 8816 |
rs574133260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148510 | GACCAGCCTGGCCAA[A/C]ATGGTGAAACCCCGT | 8816 |
rs574143674 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133551 | CAGTAGGCAGGGAAG[-/A]GGCGGGGGTACAGGC | 8816 |
rs574169207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093243 | AGGAAAGTGAAGTAT[A/G]TATGTTGGGGACACT | 8816 |
rs574183677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150507 | AGTAGTAATAACTGG[C/T]AAAGAACATTTCGTG | 8816 |
rs574196479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103189 | GATTATATAGTAGCA[A/T]ACTATTTGTGTGAAA | 8816 |
rs574261512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061997 | CTGTCTCTAAAAAAA[A/T]TTTTTTAATGAAAAA | 8816 |
rs574346973 | snp | A/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089657 | ACAAAATACCTTCTG[A/T]GGCTCTGCCTATGAC | 8816 |
rs574356725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099045 | ATCACGAGGTCAAGA[A/G]ATCGAGACCATCCTG | 8816 |
rs574391374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148985 | ATCCTGTCTGGCTAA[C/T]CTGCACTGGTCTATT | 8816 |
rs574402411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149398 | CCATTTCTCCACTTG[C/T]TGCTGTCATAATTTC | 8816 |
rs574427953 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061011 | TAAAAAAATTGAGGA[-/T]TTTTTTTTTTTTAAA | 8816 |
rs574444635 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052037 | GGTTACAGAATCACT[C/T]TCCCACTCCCCCAGT | 8816 |
rs574486803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082226 | AAAGCAATCAGAGCA[A/C]ATTTTCTTTGGAAAT | 8816 |
rs574525179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082823 | TCTCAAAAAGAGGCA[A/C]AGCTCTTCTACTAAA | 8816 |
rs574549734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088714 | CAGCCTATGACTAAA[C/T]GAAAAGTTCCAGAAC | 8816 |
rs574553046 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154921 | TACGTCTGTTCTGCT[C/G]AAGGGTGTATGCCTG | 8816 |
rs574569322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092196 | TTCTTTACCCAAGCT[A/G]ACTGCACAACCAAAA | 8816 |
rs574604609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091066 | ATTCTTAAACTGCCA[A/G]CTTTAAGTCAACATC | 8816 |
rs574605865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059987 | AGGACTTCAGTTGAC[C/T]AAACAATAAATAGGG | 8816 |
rs574681169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084178 | ACTAGCCATGCAAAC[G/T]TTTGGTGTTCTTAAG | 8816 |
rs574716643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084618 | CTGAAAAGAGATTCC[G/T]TCTACTCTTTACATT | 8816 |
rs574835137 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154504 | TAATCGTACTAATAA[C/T]AAATATGCAAATGTT | 8816 |
rs574938354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065346 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 8816 |
rs574951733 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084500 | AAAGTTGAAGGCCCG[A/G]CAAGGATTTCTCTGA | 8816 |
rs574983506 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146829 | AAATAGAAAAGGCCA[G/T]AAGAAAATTTGAAAA | 8816 |
rs575031648 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070607 | TCTAATGCTCCTTTC[A/C]ATATGTAACACTGGC | 8816 |
rs575031765 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130626 | GAAAGTTTACTACTT[A/G]TATATGTACAATGCA | 8816 |
rs575038876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075631 | GGACTACAGGCACAC[A/G]CCACCACGCCCAGCT | 8816 |
rs575051722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074985 | GTTGCAGTGAGCCAA[C/G]ATCACACCAGTGCAC | 8816 |
rs575059962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132714 | AGGTGATATAATGTG[A/G]GGCAGCATAGCACAG | 8816 |
rs575175163 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124108 | GCTCACTCCCTTAGC[-/ATA]ATGTCTTCAAGGTGC | 8816 |
rs575176907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056742 | TAAGGACAAATGCAC[C/T]TCCCTGTGGGAATTC | 8816 |
rs575176953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066051 | CTCATTCCTGAGCTG[C/T]CATTTGTTTATAAAA | 8816 |
rs575185738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057873 | TTCAGCAGTAAGGGG[A/G]GCAGGTAGGAACCCC | 8816 |
rs575219864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072253 | ATCCAAAAATATTAT[C/G]AGCATGTTATAGGCA | 8816 |
rs575228262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129630 | AGACTGACCTGCAAA[C/T]AATCCAAGTGAAGAA | 8816 |
rs575253118 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082044 | ATTTAAATCAAACAC[-/A]GCTCTTATTTTCCCC | 8816 |
rs575304884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072921 | CCCAAGTACCAAGTA[A/G]AGGATGGGGATGCAG | 8816 |
rs575327792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122946 | CTAAGTTGGTTGTTA[C/T]TGTTTTTTCCCATTT | 8816 |
rs575339264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130334 | AATAAAATAAGCCAG[A/G]CATAAAAGGACAAAT | 8816 |
rs575379364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105725 | TTGGACTCTGGGACT[G/T]GCACCAGTGGCCTCC | 8816 |
rs575398675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145856 | CTTAAGACCATAAAA[A/T]GAAGACAGAGATTAA | 8816 |
rs575414354 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134420 | TAATAGCACAGGTGA[C/T]ACTCCTTATATATAA | 8816 |
rs575452026 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111229 | GTTTCATTTAATCTG[G/T]TCTCTATAGAAGTAG | 8816 |
rs575493920 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104889 | GAGAGACAGGGGTAC[C/G]TACAAACTAAAAAGA | 8816 |
rs575533036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103329 | TCACTACCCCCAGGA[A/G]AAAACATGAAGGACC | 8816 |
rs575535710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145134 | GCAATCCTCCCACCT[C/T]GGCCTCCTGTGTAGC | 8816 |
rs575561549 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139266 | CAGGGTGGGAAGATC[A/G]CTTGAGGCCAGGAGT | 8816 |
rs575631718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084864 | TTACTGAAGTCAACT[A/G]GATTGTTCAGTATGA | 8816 |
rs575639104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113692 | CATGGAAAAGAAAAA[G/T]GGTGGTCTCTTCCCC | 8816 |
rs575675961 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076676 | TTCAGTCTGGGATGA[C/T]GAAGAAGTTCTGAAG | 8816 |
rs575694854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110541 | CCACAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 8816 |
rs575715086 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137569 | TCTAAAAAGACTGAA[A/T]CAGTGAAGGCCCTAA | 8816 |
rs575728448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094439 | TTCTGGGCAGGGAAC[G/T]CTGACCTCTCACACA | 8816 |
rs575791172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063072 | TTCCCCCCGATAGCA[A/G]GGAGAACTAAGGATA | 8816 |
rs575827797 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054842 | ATCTGGGGGTAATCA[C/T]AGTTGTCTTCTCCAA | 8816 |
rs575890173 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146573 | ATAGCAAACCAGAGG[-/A]AAAAAAAATCTATTA | 8816 |
rs575891899 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101641 | GACAGGAATATGTTC[C/T]ACGAAATGTGTTGTT | 8816 |
rs575915299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143666 | GATCAGCAGGGGATG[C/T]GAAACAATGACAGTT | 8816 |
rs575972112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128008 | ATGGTTATGTTAAAA[A/G]AGAAAAAAATCCTTA | 8816 |
rs575993389 | in-del | -/AAATAAATAATTAAATAATTA | 0.408017 | 0.193729 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107048 | TTTGTCTCAAAAAAT[-/AAATAAATAATTAAATAATTA]AAATAAATAATTAAA | 8816 |
rs576044098 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087447 | ACTATATTGCAAGAC[C/T]AGAAGGTAGGCTTGC | 8816 |
rs576092426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143052 | AAACATCAGAATCTA[A/G]GTGAGGTGAGTGCTA | 8816 |
rs576194880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149586 | ATATTATTTCTGCCC[C/T]GGGTATAAGTTAATT | 8816 |
rs576206952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150458 | AAAATAGAGTTCATT[C/T]AAGATACAGGGGAGC | 8816 |
rs576232564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070965 | ACTACACCTGGCTAA[C/T]TTTTGAATTTTTAGT | 8816 |
rs576238303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135897 | GATGTTATAAAATGA[C/T]GCATGGGAGGAAAGA | 8816 |
rs576266897 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070008 | GTATTATTGTTGTTG[G/T]TGGTGGTATTATCCT | 8816 |
rs576296534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060303 | GAACAAAGGGCAGGG[C/T]TCTATCCTAGCTTTG | 8816 |
rs576328634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136544 | CTCGCTATTTTTTTT[A/T]AATTTTGGAAAATAT | 8816 |
rs576333563 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061084 | GAACATGGTTCACTG[C/T]AGCACGACCTCCTAG | 8816 |
rs576348814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062594 | GCAGATAAACAGCTC[C/T]GAATGGGAGCAAAGA | 8816 |
rs576410945 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095372 | AATGAAATACATCTA[C/T]CCCAACCTATCTTCA | 8816 |
rs576411235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084146 | ACAGGGGTCCTTATT[C/G]TCTCACCTACTAGAG | 8816 |
rs576435338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142239 | TGGAGGGTCAAAGCT[A/G]CAGTGAGCCGTAACT | 8816 |
rs576454366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075931 | TTAGCTAAAACTCAG[C/T]AACGACAACAAAAAA | 8816 |
rs576455557 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154906 | TCTGAGAGCAGGGAC[C/T]ACGTCTGTTCTGCTC | 8816 |
rs576498938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134338 | AAAACCCGTGACTTA[C/G]ACTTTATAGTAATGT | 8816 |
rs576520305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117305 | CTGCTACTTCGTGCT[A/C]CCTTACCTGCCTAAC | 8816 |
rs576520350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126947 | AAAACCAAAACTATA[A/G]AACTCCTAGAAGATA | 8816 |
rs576545536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109041 | TCTTTTTTTAAATTT[A/T]AAGATACAACATAAT | 8816 |
rs576555859 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128640 | AAACAGAATATTGTG[C/T]GCCTGTAGTCCCAGC | 8816 |
rs576582862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101138 | ACACAATCAAGCAGC[C/T]GAAATAGAAGCAAGT | 8816 |
rs576592191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148897 | CTCCAACTCAAATCA[C/G]ATGACATCAAATCCC | 8816 |
rs576601306 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053359 | TTCTTCCAGCATAAA[C/T]CTACAACTCACTGGC | 8816 |
rs576726404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148503 | AGTTTGAGACCAGCC[G/T]GGCCAACATGGTGAA | 8816 |
rs576777514 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087318 | CAGAATGTACCCAGT[C/T]AGGCTTCAGGGAGAA | 8816 |
rs576788638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107653 | CTCTCTGCCACATAA[C/T]TAATTGACGGTGGCA | 8816 |
rs576802065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096636 | ACGCTTCAACTTTTT[A/T]GGCCCACAGGTTCCA | 8816 |
rs576834840 | snp | C/T | 0.000512435 | 0.0159986 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118272 | AAACACGTCCAATGT[C/T]TCACTGCTGGGAGAT | 8816 |
rs576876352 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058616 | GTGGTGGCTCACACC[C/T]GTAATCCCAGGACTT | 8816 |
rs576937334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141426 | TGTTACATATGTATA[C/T]ATGTGCCATGTTGGT | 8816 |
rs576938873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097915 | TATTGAAAGAGCTTC[C/T]TAGCTTGTCTCTGCT | 8816 |
rs576963734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095941 | CATCAGAGCTGGTGT[C/T]GTATCCCAAGTAGAG | 8816 |
rs576976340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132499 | TACCACTTTTCTATT[A/C]ACTCACCCCATCCAG | 8816 |
rs577036059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123950 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 8816 |
rs577036729 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140275 | CTGTCTAAAAAAAAA[-/AG]AGAGAGAGAGAGAGA | 8816 |
rs577038421 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056054 | CACAGAGAGGTACCA[C/T]TTTTCCCAAATGAAA | 8816 |
rs577125532 | snp | A/T | 0.000798881 | 0.01997 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090894 | TGTTGTGCTTGAGAA[A/T]AAAAAATTCTATTTG | 8816 |
rs577145869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087943 | GAGCAGAATAGGTAT[A/G]GTGCACAGATTTGTT | 8816 |
rs577229840 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069721 | TTCAACTGATCTTCC[C/T]GCCTCAGCCTCCCAA | 8816 |
rs577248130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072104 | CCCACAGCCCCATTT[C/T]CCTATTTGGCTTTTA | 8816 |
rs577304678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105476 | GCTGCTGAAGCATTG[C/T]TGCTGTGTGTGTCTG | 8816 |
rs577367923 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090151 | AAGTTGACAAAGGAT[A/G]GGAAATCAACAAAAG | 8816 |
rs577389895 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110676 | CACCCAGGAGATCGA[C/G]ACCAGCCTGGGTAAC | 8816 |
rs577409449 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153420 | CGCCGGGCGGAGACC[C/T]CTCTGCACCCCAGCG | 8816 |
rs577417454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104838 | CTCCAGCCTGGGCAA[C/T]GAGAGCAAAACTCTG | 8816 |
rs577503362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080811 | CGTTCATATTTAATA[C/T]ACTACTGTGAAAAAA | 8816 |
rs577505956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074065 | TTAGTAACTAGACCA[C/T]AGCAAATGTTGAGTT | 8816 |
rs577521245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065313 | TCTTAGCCAGGCTGG[C/T]CTTGAACTCCTGACC | 8816 |
rs577566921 | in-del | -/GAAA | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154621 | AATTTTTAAAAGAAA[-/GAAA]TCAAATTCCAAAAAT | 8816 |
rs577578847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121429 | ATGACTCCAAGATCA[C/T]AGGTAGAATGAACCA | 8816 |
rs577620585 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079633 | ATAAGGACAGAAATA[A/C]AAGTGAGGTCATTCC | 8816 |
rs577645805 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145035 | CTTTTCATTTTTGCC[A/C/G]TATCAACATAACACT | 8816 |
rs577664453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129523 | AAGCAAGGGAAAGTC[A/G]GTTCAGACGCAAAAG | 8816 |
rs577702765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127892 | AGTAAATTTAACAAA[C/T]CATCAACATTTTGTC | 8816 |
rs577771884 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143838 | CCCCTAGAATTACGT[A/T]TCACATCATTTTTTT | 8816 |
rs577790155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136771 | TGTTCCTAAATATCC[C/T]ATAGTGCACAGGACA | 8816 |
rs577804379 | in-del | -/A | 0.00119784 | 0.0244435 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090894 | GTTGTGCTTGAGAAT[-/A]AAAAAATTCTATTTG | 8816 |
rs577853628 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141454 | GGTGTGCTACACCCA[G/T]TAACTCGTCATTTAC | 8816 |
rs577895306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121993 | CTGCCAAAGAGAAAT[A/G]AAGAAAAAGACAGGT | 8816 |
rs577922196 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093589 | CTATCCTATCCTATG[C/G]GAAGGGAAGCCCTGA | 8816 |
rs577930391 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120252 | CTATGCCTGGCTAAT[A/T]AAAAAAAAAATTTTT | 8816 |
rs577989760 | snp | C/T | 0.000131833 | 0.00811782 | missense | DCAF5 | GRCh38.p7 | 14:69054179 | GGACGAGGGTGTAAG[C/T]GTCCATTGTTGTGGT | 8816 |
rs578001657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063012 | ACAAAACAAAAAACC[C/G]CATAAAAACCAAAAC | 8816 |
rs578026926 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087994 | GAATTTGTTGTAATA[C/T]TTTAAAACCAAGAGA | 8816 |
rs578035636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062207 | CAGGTACTGTCACTA[C/T]GCCTGGCATCACTTT | 8816 |
rs578086612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144424 | AAAAATACAAAAAAT[A/T]AGCTGGGCGTGGTGG | 8816 |
rs578098034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152127 | CTGTATTAAAAACAA[C/G]ACGCAGAAGAGGCCA | 8816 |
rs578117228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069921 | CCACTGTGCCCAGCC[A/G]AGAAGGCTTTCTTAG | 8816 |
rs578120442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086544 | CCCATTAAAAGTATA[A/T]CTTTATTTCAGATAA | 8816 |
rs578124543 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114726 | AAACCAATAAATGTC[A/G]CTGTAAAAATACAAT | 8816 |
rs578142879 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075091 | AAATAAGGGACATAA[A/G]GGAGTTCTATGAAGT | 8816 |
rs578167475 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134160 | TCCAAGAGCACACTG[C/T]CAGTTACAGGCAGAG | 8816 |
rs578199239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094291 | CAGGCCTGTAGAGGA[A/G]TCTGCCCAGGACAGG | 8816 |
rs578221635 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130868 | GACTTGATTCAAATC[C/T]TGGTTTCGCCATTCA | 8816 |
rs578224333 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131639 | ATCCAAAGAGCTTGG[C/T]CTGGAGCCTAAAACT | 8816 |
rs745346290 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054550 | GGCCATTGCTATGTT[C/T]AGACAGGCTTCCTTA | 8816 |
rs745412745 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147751 | AATTAATACTTTGAA[A/G]CATCATAGTTGCTCA | 8816 |
rs745435862 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054475 | GCTGGGAGTTCTAGG[A/G]GTCTCTTCTTTAAAA | 8816 |
rs745472656 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086911 | TAAGAGATCTCAGTG[C/G]TCAGGTACGCCAGTG | 8816 |
rs745560240 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101599 | AGATAAATCTGGATA[C/T]GTTAATACAGTCATG | 8816 |
rs745560338 | snp | A/C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086228 | CCGGGCGTGGTGGCG[A/C/T]GTGCCTATAATTCCA | 8816 |
rs745640479 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141017 | CGGGCACCTCTAATC[C/T]CAACGGGATTACAGG | 8816 |
rs745665061 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088195 | CTGTCTTGCTCCTGT[A/C]CGCAACAAGTTGTGA | 8816 |
rs745674378 | snp | C/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090569 | CAACAGGCATTTATT[C/T]GGCTCCTATTACATC | 8816 |
rs745678311 | in-del | -/CT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141501 | AATGCTATCCCTCCC[-/CT]GTCCTGCCACCCCAC | 8816 |
rs745727022 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114228 | GATGTAGCAAAGTCC[C/G]TACAGATATTTTTGC | 8816 |
rs745732516 | snp | G/T | 2.05814e-05 | 0.00320785 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053810 | TAAACAATTTTTTTT[G/T]TTTTGTAAGGCTACT | 8816 |
rs745761226 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064775 | GATGAGAATAGAACT[A/G]GATCTGTCTTACCTA | 8816 |
rs745808597 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054913 | TTCTCGGGTTGTCTT[C/T]TGTCGGCGCCGCATG | 8816 |
rs745852949 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078822 | AGTTCTAGAGATGGA[C/T]AGTGGTGATGGTTAC | 8816 |
rs745909310 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054802 | AGGGGACGAGGTTGG[A/G]GAGGAGGAGAGGTCA | 8816 |
rs745909843 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130876 | TCAAATCTTGGTTTC[A/G]CCATTCATGTGTCCT | 8816 |
rs745998730 | snp | A/C | 0.000184723 | 0.00960872 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091183 | AAGAAAAAGAGTCAG[A/C]ATCTGGCTCCCTCTC | 8816 |
rs746013842 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144251 | AAAAAAAAAAAGTTA[A/C]ATAATAATTTTCATT | 8816 |
rs746019530 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103921 | TCCTTAAAGTTCATC[A/C]AAGTTGTATCAACAC | 8816 |
rs746020540 | in-del | -/TTTTTTTTTGA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067353 | TTTTTTTTTTTTTTT[-/TTTTTTTTTGA]GACAGGGTCTCACTC | 8816 |
rs746033603 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118465 | AAAAAAAAGGTACTA[C/T]TAAGGAGTCTTTTTA | 8816 |
rs746044894 | snp | A/G | 4.96479e-05 | 0.00498212 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69053959 | ATGAACAGCCCTGCT[A/G]CTATCTGTGGCTGGG | 8816 |
rs746067752 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149865 | CACTCAGGTGTTGAC[G/T]GCTAATGAGAGACAA | 8816 |
rs746100205 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117163 | AGAAAGCACTTCTCA[A/G]TCTATGACCTCCATA | 8816 |
rs746167693 | snp | A/G | 0.000173964 | 0.0093248 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152949 | CACCACTGACCTCAT[A/G]CTGCCCCCCAGGCCA | 8816 |
rs746185263 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066291 | AGGCGCACACCACCA[C/G]GCCCAGCTAATTTTT | 8816 |
rs746273471 | snp | A/G | 1.65031e-05 | 0.00287251 | missense | DCAF5 | GRCh38.p7 | 14:69055280 | TCTACTGTGGGAGGC[A/G]GGGAGCGAGGCAATG | 8816 |
rs746287363 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054109 | GTGTCCTGGGGAAGA[A/G]TAGGCCACCACCTCC | 8816 |
rs746354784 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061329 | TGGCAGGAACATCAC[A/C]TATTCTTACTTAAAA | 8816 |
rs746363391 | snp | A/G | 1.65236e-05 | 0.00287429 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055216 | GGCTACTGTGTTTGT[A/G]GTGGTGACCCGCAGG | 8816 |
rs746417120 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059760 | GCTGAGGACTCCAGA[A/G]CTTTTTGCTTTCCTT | 8816 |
rs746464956 | snp | A/G | 1.65053e-05 | 0.0028727 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062371 | AAAAGGACAGAAGGG[A/G]AAGGTGCCTCACCTT | 8816 |
rs746491410 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113018 | AAGTCTTCTTTAGAG[C/T]TGACATTTTTTTTTT | 8816 |
rs746509209 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063535 | CCCTCTTAGTCCCTA[C/G]CAGGAGCATGGCGCC | 8816 |
rs746530446 | in-del | -/AAAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074400 | AAACCATCCTAAGAA[-/AAAG]AAAAGGGGGGGGAAA | 8816 |
rs746554717 | snp | A/T | 1.648e-05 | 0.0028705 | missense | DCAF5 | GRCh38.p7 | 14:69055538 | TCTTCATGGGTATAG[A/T]GGCAGCGGGAATCGT | 8816 |
rs746580690 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100080 | AGGTATTAAATACAT[A/G]TCCTACCCAATTATG | 8816 |
rs746581237 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111879 | TGACCACTCATCACC[A/C]CTAAAATCCCTAAAG | 8816 |
rs746612413 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084746 | ATCTTGGCCATTCAT[G/T]GAAAGCAAAAGCAAA | 8816 |
rs746642745 | snp | A/G | 3.31011e-05 | 0.0040681 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119260 | AGCAGACATCTGATC[A/G]TTCGTGCAAGGTGGT | 8816 |
rs746682215 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147311 | ATGTTAGATGTTGAA[A/G]GTATCAATCTCCTGA | 8816 |
rs746704584 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098085 | TTATAATGCCAGCAA[C/G]GCCCTAGACAATACC | 8816 |
rs746730769 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064542 | CTTTCCACCATATCA[A/G]CTGCCTTTGGAAGAT | 8816 |
rs746738523 | snp | C/T | 1.66563e-05 | 0.0028858 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118312 | AGACAGAGGCACACA[C/T]ATACACACAAGCATA | 8816 |
rs746773788 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138400 | AGACTCAACCAGAGT[A/G]ACAGTTGGCCTCCAC | 8816 |
rs746790944 | snp | C/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088201 | TGCTCCTGTCCGCAA[C/G/T]AAGTTGTGATCATTT | 8816 |
rs746804349 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105179 | GGTTCTCAAAAAAAA[C/T]TTGTTCACGAATGTT | 8816 |
rs746868695 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060875 | CTGCCATGAAGTACA[A/G]TTTGATTTAGCTCTG | 8816 |
rs746868899 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081054 | GAGGAAAAAATAAAT[-/A]ATAAGATTTAAAAGA | 8816 |
rs746903261 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077069 | ATTGTCTAATAGCAA[C/T]GAGAGAGTAATTTTG | 8816 |
rs746928087 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139940 | GAAGGAAGGGAGGGA[A/G]AGAAAGGGAAGGAAA | 8816 |
rs746932417 | snp | G/T | 4.8968e-05 | 0.00494789 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091155 | CATTTCCAGTTGTGA[G/T]GCTGGCAGTAAAAAG | 8816 |
rs746935967 | in-del | -/GGGAGGGTGCG | 4.18034e-05 | 0.00457165 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152720 | CGAGAGGGGGAGGCT[-/GGGAGGGTGCG]GGGAGGCGCGGGGAG | 8816 |
rs746956032 | in-del | -/CTG | 1.6473e-05 | 0.00286988 | cds-indel | DCAF5 | GRCh38.p7 | 14:69055003 | CTAGAGCTGCTGGAA[-/CTG]CTGCTGGATTCATCT | 8816 |
rs746961938 | snp | A/G | 1.65064e-05 | 0.00287279 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054697 | GCGGAGCCACTTGTA[A/G]GCTTTATAAATTTTT | 8816 |
rs746984512 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089414 | AAAGTTAGATTCAAT[A/G]ACTTTGCATCTTCTT | 8816 |
rs747034308 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143253 | AATGAAGGAGAAAAA[A/G]AATCAGATCCTTTAA | 8816 |
rs747066839 | snp | G/T | 1.79674e-05 | 0.00299722 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091007 | GTCACTGACACTTCA[G/T]AACTTCTATGGTTAA | 8816 |
rs747069990 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093334 | AGGTAGTGATCCCAG[C/T]AGTTTTAGAGAAAAA | 8816 |
rs747084974 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128311 | CCTGCCTCGGCTCCA[C/T]GGGTAGCTGGGACTA | 8816 |
rs747113739 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081001 | AAACTCACTTCATGT[C/T]CTGCTTTAGTACTAA | 8816 |
rs747151130 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065752 | TTGAAATAGCTAAAG[A/T]CAAAATGCCAATATC | 8816 |
rs747158762 | snp | A/G | 1.70574e-05 | 0.00292035 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152938 | GACAAGAAGCCCACC[A/G]CTGACCTCATGCTGC | 8816 |
rs747168920 | snp | A/G | 3.29598e-05 | 0.00405941 | missense | DCAF5 | GRCh38.p7 | 14:69054168 | GAGGGTGAGGGGGAC[A/G]AGGGTGTAAGCGTCC | 8816 |
rs747177028 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141575 | CCTTTTTAAGAATGA[A/C]AGGAACACTAATAAT | 8816 |
rs747182193 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081634 | CTCAATAGATTTCAG[A/G]AAGGAACCACCATCA | 8816 |
rs747188899 | snp | A/G | 1.71416e-05 | 0.00292755 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152769 | GGTTGATTTACCTGA[A/G]ACCAGCCACTGGCCT | 8816 |
rs747272063 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094691 | TTGCCGGGAAGGCAA[A/C]GCTTGGAAGCAGTCT | 8816 |
rs747286134 | snp | A/G | 1.65056e-05 | 0.00287272 | missense | DCAF5 | GRCh38.p7 | 14:69055181 | GCTGCATCCTCACAC[A/G]TGGGTGTTGGTGGAG | 8816 |
rs747302319 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120942 | GCAGGGTGAAAGTAC[A/G]TGGAGAAGGAGACCT | 8816 |
rs747327045 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085978 | TGCTAACAATTCGAT[C/T]TGCCGTTTCACACTA | 8816 |
rs747355767 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112546 | TCTAAAAATAAAAAC[-/T]AAAAAAAAGAAAAAA | 8816 |
rs747411820 | snp | A/T | 1.66277e-05 | 0.00288333 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116544 | AGGTACCTGTGGGCC[A/T]CTGGCAGGCAGATAA | 8816 |
rs747436601 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | DCAF5 | GRCh38.p7 | 14:69055080 | CCACCTCACAGACAT[C/T]CTCCTCAGAATCGGA | 8816 |
rs747442027 | in-del | -/TGTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121936 | ATATGTGTGTGTGTC[-/TGTG]TGTGTTTCTGTGTAC | 8816 |
rs747477564 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058433 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8816 |
rs747481386 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108363 | AAGAAAAATCAAGAA[A/G]ACAGGAGAAAGCATC | 8816 |
rs747490585 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107812 | TATTTTCTAAAAGTT[A/G]GCTTTGACTATTTTG | 8816 |
rs747529599 | snp | C/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154876 | ATATGAGTCTCCCCA[C/G]TCTGCTGTAAGTTCT | 8816 |
rs747608984 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075934 | GCTAAAACTCAGCAA[C/T]GACAACAAAAAATGA | 8816 |
rs747664048 | snp | A/G | 1.66161e-05 | 0.00288232 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118302 | TAAGAGAGCAAGACA[A/G]AGGCACACACATACA | 8816 |
rs747764064 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063325 | TTATGAACTTGGGAT[A/G]AATTCAAAGTTTCCA | 8816 |
rs747779219 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096372 | TTCCCCAGAACATGA[C/T]TCACTGCCACATTTC | 8816 |
rs747834181 | snp | A/G | 3.2993e-05 | 0.00406145 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118148 | GCCTACCTCCATGGG[A/G]GGATTCCCGAATGTC | 8816 |
rs747848395 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144768 | CTTTCAATTCCTTAG[A/G]ACAGATCCAGAAAAT | 8816 |
rs747852341 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061912 | TAGTTCCAGCTACTT[C/T]GGGGGGCTCAGGCAG | 8816 |
rs747885476 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076853 | GGAGCTTCCCAGAGA[A/T]CTTTCACGTAAGGCC | 8816 |
rs747914219 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116872 | AGGGTTATTATGCTT[G/T]TAATCCAATTGTATT | 8816 |
rs747923556 | in-del | -/CCC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071042 | ACTTCAAGTGATCTG[-/CCC]CCCTCAGCCTCCCAA | 8816 |
rs747924164 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149669 | ATGAAATGAAAACAA[C/T]GAACAAACTATGAAC | 8816 |
rs747929279 | snp | A/G | 3.30311e-05 | 0.0040638 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054673 | ATTTGAGTAGGAGAT[A/G]TAAGAGTAGCGGAGC | 8816 |
rs747947047 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064247 | AAAAGTTCCTTTGGG[C/T]CTATTTCTTCTAGAT | 8816 |
rs747969444 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146504 | GCCATCTCTACAGGC[A/C]TTCTTTCTTTCCCAC | 8816 |
rs747976607 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087946 | CAGAATAGGTATGGT[A/G]CACAGATTTGTTTCA | 8816 |
rs747980324 | snp | C/T | 2.81932e-05 | 0.00375444 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075446 | ATAGATAACATTATA[C/T]ATTATAATATAGAAT | 8816 |
rs747999094 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116888 | TAATCCAATTGTATT[A/C]GTTTTAGAAAAGTTT | 8816 |
rs748000887 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69115988 | ACTCAGCAGCAACAA[A/G]TTTGGCAAATCTCCA | 8816 |
rs748005578 | snp | C/G | | | missense | DCAF5 | GRCh38.p7 | 14:69055145 | TAGCGCCGCAGAGCA[C/G]ACAGACGCTGCTGGC | 8816 |
rs748027057 | in-del | -/ACC | 0.000469733 | 0.0153182 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152984 | CCTCTTCATGCTGGA[-/ACC]ACCGCCGCCGCCGCC | 8816 |
rs748037980 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151134 | AGAGGTCTTCCCCCA[G/T]TTTTGCTCTTCAAAT | 8816 |
rs748055021 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081438 | CACATTCTGATTCAC[A/C]TCACTTTTCATTCAT | 8816 |
rs748068372 | snp | C/T | 1.68724e-05 | 0.00290446 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152925 | CAAGCCCCGCTGGGA[C/T]AAGAAGCCCACCACT | 8816 |
rs748098453 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137329 | TTCCAGATCACAAAT[C/T]TTCTTCATCTCCAGC | 8816 |
rs748105922 | in-del | -/CAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104209 | ATTACATATTCCCAC[-/CAG]CAGCAATATGTGAGT | 8816 |
rs748113419 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103627 | CATGCATTCATTTGT[A/G]TTAGGTGAATGTGAT | 8816 |
rs748147598 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087256 | TTTTAACCCTATTAA[A/G]AGACTCGCTCACTGA | 8816 |
rs748162284 | snp | A/G | 2.121e-05 | 0.00325647 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152747 | GGAGGCGCGGGGAGG[A/G]GAAGGGGGTTGATTT | 8816 |
rs748220507 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082981 | TGTCACCAGATTACA[C/T]CAATTCCACTTGTTC | 8816 |
rs748226767 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107423 | AATAATGGCAGAATC[A/G]AAGGTCCCACCCCAA | 8816 |
rs748265993 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056972 | CCAGCTTCATAATCT[C/T]ACCCTAGAGAGTTTC | 8816 |
rs748298489 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153818 | TCCTTTAGTTGAAAA[A/G]GGCTAAATTGTTCCG | 8816 |
rs748304211 | snp | C/T | 3.30929e-05 | 0.0040676 | missense | DCAF5 | GRCh38.p7 | 14:69054005 | TCTCTTGTTCCAGCA[C/T]TGGGGGTCTCACAGG | 8816 |
rs748325771 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133214 | GGTACACAGCTACCA[-/AG]AGTCATTGTTGGCAT | 8816 |
rs748328566 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | DCAF5 | GRCh38.p7 | 14:69055057 | GGGAAAGAGATCTGT[G/T]TCTAGTTCCACCTCA | 8816 |
rs748372685 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141242 | GGCATCCCATAGTGA[A/G]TGTGAGGAGCTAAGA | 8816 |
rs748418212 | snp | A/C | 1.67086e-05 | 0.00289033 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116334 | AATGAGGCAGAGGAA[A/C]GTTTTAACACCTATG | 8816 |
rs748486346 | snp | C/T | 4.94173e-05 | 0.00497053 | missense | DCAF5 | GRCh38.p7 | 14:69054925 | CTTCTGTCGGCGCCG[C/T]ATGGCATTCCGCTGC | 8816 |
rs748507814 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083473 | CGGCAGTGGAACCTA[A/C]AGTTGCAGGGGGCCT | 8816 |
rs748575373 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146127 | ACACTTCCTTTCAAT[C/G]TGGTGGCCAAAATAC | 8816 |
rs748598783 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105372 | ATCTCAAAAACATGA[C/T]GCTAAGTGAAAGAAG | 8816 |
rs748599177 | snp | C/T | 1.93246e-05 | 0.00310836 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091866 | TTGGAGGGACAGGTT[C/T]CCACCATAGCGCAGG | 8816 |
rs748628875 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119130 | TTTTAGTCTAAAGAG[A/G]TATTTGCCTCTTCAT | 8816 |
rs748680092 | snp | C/G | 1.6591e-05 | 0.00288015 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118093 | CAATGAATCTGACAT[C/G]AAACTGTTCAACACA | 8816 |
rs748693666 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084499 | AAAAGTTGAAGGCCC[A/G]GCAAGGATTTCTCTG | 8816 |
rs748769287 | in-del | -/ATTA/ATTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097584 | ATTATTATTATTATT[-/ATTA/ATTT]TTTTTTTTTTTTTTT | 8816 |
rs748786728 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062336 | AGTTTCTTCTAATTA[C/T]AAATTGTGAGAATTT | 8816 |
rs748786880 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097435 | TATACTGCATCCTCG[C/T]ACACCCACATTAATT | 8816 |
rs748804915 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087078 | GAGGCAAACATGCTT[G/T]CTAGACTGAAAGACT | 8816 |
rs748807827 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137185 | TTCCATAGTAAAGTA[C/T]GGAATTAGTGACACG | 8816 |
rs748808467 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135989 | ATTCGATATGGTTTT[A/C]TATTCTACATTGCAA | 8816 |
rs748812538 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053187 | TTAAGTGCTAAACCT[C/T]TCATTAGCATTAAAA | 8816 |
rs748872443 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149537 | GATGTATTATTAACT[A/G]ATAGTACTTTACCCA | 8816 |
rs748891914 | in-del | -/A | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090377 | GTGGGCACCCCAAGG[-/A]GACATCACTGAGGCC | 8816 |
rs748900985 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069104 | CCAGTTACATGGGAG[A/G]AAAAAGCAGATACCT | 8816 |
rs748991903 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123181 | TATACAAAAGCTAAT[A/G]CAGAAAGATGTCCAA | 8816 |
rs749039611 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064841 | AAGTCCACCAGGTGC[A/G]TAAATACTTGCTGAA | 8816 |
rs749086907 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114378 | CCATATAGTCATTAA[A/C]AGAAGGGGCTAGATC | 8816 |
rs749087114 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121787 | ACCCTAACACAACAC[C/T]TTTCAAACAGGAGCC | 8816 |
rs749087823 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062438 | GGTGTGGGGATTAAA[C/T]CGGACTTGGTTAACA | 8816 |
rs749122446 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101806 | GAACACCAAATGCCA[C/T]AGGCAACTGTAACAC | 8816 |
rs749142827 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066536 | GGGGGGTAGGGAAGA[C/G]TATAACCATATCTAT | 8816 |
rs749160751 | in-del | -/TTTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067339 | GCCGATTTCGTATCT[-/TTTTTTTTTT]TTTTTTTTTTTTTGA | 8816 |
rs749185511 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052147 | GCCGCATTACACACA[C/G]CAGGCACATCTTCTC | 8816 |
rs749186043 | in-del | -/TC | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051278 | CTGCTATTAAAAATA[-/TC]TATTATGGAAGAAAT | 8816 |
rs749220088 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122311 | GGGCTTGACCCTGGA[A/G]TGGATGGCTTGTTCC | 8816 |
rs749258757 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115566 | TAGCTAGCAATACAC[A/G]GAAGTTTTTTAATAC | 8816 |
rs749309506 | in-del | -/TTTAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124713 | TTGGGTTTTTGTCAC[-/TTTAT]TTTAATGAAAAATGC | 8816 |
rs749325911 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136079 | TCTAAGACATTAACA[C/T]GCTCTTCCCTTTTAT | 8816 |
rs749326559 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151539 | ATCCCTCCCAATATA[A/G]GAAAAGGGACAGAAG | 8816 |
rs749334022 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084291 | ATGGGATCAACATCA[A/C]TGTGGTCACACCAGG | 8816 |
rs749335199 | snp | C/T | 4.9423e-05 | 0.00497082 | missense | DCAF5 | GRCh38.p7 | 14:69055034 | TCGGGGCTGGGTGAC[C/T]GTGGCCGGGGAAAGA | 8816 |
rs749359867 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118563 | TCATTTATTACAGAA[G/T]GCATCTGCTTGTGTA | 8816 |
rs749389656 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068903 | CTGGAGACCACATAA[C/G]TACTTAAGAAATGAG | 8816 |
rs749400076 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139277 | GATCGCTTGAGGCCA[G/T]GAGTTCAAGACCAGC | 8816 |
rs749407536 | in-del | -/GAG | 4.94193e-05 | 0.00497064 | cds-indel | DCAF5 | GRCh38.p7 | 14:69054782 | GCGTGGAAGTGCTCC[-/GAG]GCTCAGGGGACGAGG | 8816 |
rs749416958 | snp | C/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089478 | GTCTTGTCTGTCAGA[C/G]AGAATAAAATACCCA | 8816 |
rs749444029 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117318 | CTACCTTACCTGCCT[A/T]ACCCTAAAAACAAGC | 8816 |
rs749446130 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132481 | CCTACCCTGAAATTC[A/G]GTTACCACTTTTCTA | 8816 |
rs749473481 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107205 | AGGCATTCCCCAGAT[A/G]CTCTGGTCTGAAGCG | 8816 |
rs749488904 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056709 | TCTAGACCAAGACTT[C/T]GTTTCCCCAAAGCTA | 8816 |
rs749527985 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138573 | GTCCTTTTTAAATGC[A/G]GAACCTCATGACTTT | 8816 |
rs749531140 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070073 | TTCCAAAGCCCCCAG[G/T]TGGAAGATAAATGGA | 8816 |
rs749578966 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69055657 | AGGAGTAACTGGAAA[A/G]TATTCTTTCACTGGT | 8816 |
rs749625855 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061654 | GATTCTGGCAATCAG[C/T]AGTTTTATCCATGCC | 8816 |
rs749634349 | in-del | -/TTAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072750 | ATCTTAAAAGATACT[-/TTAG]TTAGTTACATACAGA | 8816 |
rs749642558 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095284 | CATTCAAATGAGATG[A/G]GCAATATATTGAAAG | 8816 |
rs749644564 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111580 | CAGCTAAAACCGGCA[A/G]TGAAAAGGATGAGAC | 8816 |
rs749756517 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083399 | ACTGCTTGGACAGGA[C/T]GTCTCACCTGCTGAT | 8816 |
rs749796983 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082250 | TGGAAATGGGCAAAG[C/T]CGTAGATTTATTTTA | 8816 |
rs749805670 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145911 | ATGGAAGTGCTCTTA[C/T]AAACTTATGCTCTCT | 8816 |
rs749818069 | snp | A/G | 8.23852e-05 | 0.00641762 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055516 | GTTCAGCACAAGGCT[A/G]ATGTACTCTTCATGG | 8816 |
rs749889949 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130169 | AGGTAAGGATTTGCT[G/T]TGGGTTTCCTCAAAA | 8816 |
rs749901336 | snp | A/G | 1.69289e-05 | 0.00290933 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075431 | TGGAACAAAAAATAT[A/G]TAGATAACATTATAT | 8816 |
rs749912080 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141277 | GGGGTTTTGGTTTTA[C/T]TTGCATACCAGACAG | 8816 |
rs749948719 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081326 | TGTTTGGTTTTGTGG[A/G]TAAGGTGGGAAATAT | 8816 |
rs749991042 | snp | A/G | 3.3279e-05 | 0.00407902 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152867 | TTCTGCAGCCCCGCA[A/G]GCGTCTCCTCTGAAA | 8816 |
rs750013634 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108606 | TCAGCCAGGATGATT[A/G]TAAGACAGACGATGA | 8816 |
rs750017483 | in-del | -/AAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072359 | TATTACTTTGATAAA[-/AAG]AAGAAGTACTTAATT | 8816 |
rs750018785 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052985 | CACTATGCCTCGATC[A/G]ATCATGGGAGCCAAG | 8816 |
rs750019238 | snp | A/G | 1.66679e-05 | 0.00288681 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062562 | AAATGAATGAAAGTA[A/G]ATAGGTTCCAGTAAT | 8816 |
rs750030176 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075159 | CATCATTTATGTCAG[A/G]TAAGACTATGTCTGA | 8816 |
rs750039029 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122037 | AAAAAGAGAAGAGAG[-/AA]AAGACACACACTATC | 8816 |
rs750047106 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067526 | TTTTTTGTACTTTTT[A/G]TAGAGATGGGGTTTT | 8816 |
rs750049660 | snp | C/T | | | intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69149454 | CTTCCTGATTTTCTC[C/T]GGTTTACTCAATATC | 8816 |
rs750051777 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102970 | TTACACCAACGTCAC[C/T]ACAAACACATGAAGA | 8816 |
rs750083634 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116563 | GCAGGCAGATAATCA[G/T]GAATGTGAATACAGG | 8816 |
rs750141335 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066418 | GGGATTACAGGCATG[A/G]GCCACTGCACCTGGC | 8816 |
rs750163325 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | DCAF5 | GRCh38.p7 | 14:69055136 | TTGTCTTGGTAGCGC[C/T]GCAGAGCAGACAGAC | 8816 |
rs750181584 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108225 | CTGTGCCAAAATAGT[A/G]CCAGGTGCCGGGGGA | 8816 |
rs750198376 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073453 | TACTTCGTTATTGCA[A/G]CTCTGGCAGACTAGA | 8816 |
rs750204731 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124723 | GTCACTTTATTTTAA[C/T]GAAAAATGCACAAAT | 8816 |
rs750214119 | snp | C/T | 1.65455e-05 | 0.00287619 | missense | DCAF5 | GRCh38.p7 | 14:69053943 | TGAGGCCACTGTGGC[C/T]ATGAACAGCCCTGCT | 8816 |
rs750264302 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058040 | TGAATGCCTCAACCA[A/G]AATGTTAAAACCCAC | 8816 |
rs750286629 | snp | A/C/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154301 | AGTTAGCAGGAATTA[A/C/G]ATCCTCTGGACCAGA | 8816 |
rs750299918 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055021 | GCTGGATTCATCTTC[A/G]GGGCTGGGTGACCGT | 8816 |
rs750304848 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096383 | ATGATTCACTGCCAC[-/A]TTTCTCTGGCTTGAT | 8816 |
rs750308164 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128945 | CAACATAGTGAGACT[A/T]TGTCTCTACTAAAAG | 8816 |
rs750311634 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116454 | CAGGGTTAAACATGA[C/T]ACTATGAAAGGCTGA | 8816 |
rs750319097 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080149 | TGGAAATAAAGATTA[C/T]TTCAAGTGAGCTGAG | 8816 |
rs750392703 | in-del | -/TAAATAAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107051 | GTCTCAAAAAATAAA[-/TAAATAAT]TAAATAATTAAATAA | 8816 |
rs750401512 | snp | C/T | 3.53613e-05 | 0.00420469 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091923 | GAATCAGGCATGAGA[C/T]AGGCTAAACAAGAGT | 8816 |
rs750449077 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064083 | CTGCCATGGTGGGAA[C/T]CCCTAGCACTGGCTT | 8816 |
rs750491442 | snp | A/G | 8.30461e-05 | 0.0064433 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091821 | CAGGAGCTGGGTCCC[A/G]TTGCTGTTGAATCGT | 8816 |
rs750491708 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063039 | AAACCACTGGGGGAA[A/G]TAATAGAGAGAATAC | 8816 |
rs750498644 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112349 | TATGACAGGTCCATA[C/T]TGGAAAAATTTGAAA | 8816 |
rs750520721 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085806 | AAACATTCACGCTCT[-/AA]AAAAGACATACAAGG | 8816 |
rs750651551 | snp | C/G | 1.64933e-05 | 0.00287165 | missense | DCAF5 | GRCh38.p7 | 14:69054288 | GAGTGGAGCCAGATG[C/G]CTTGGGGACAGGAGG | 8816 |
rs750695835 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132278 | CGTACAAGAGTTCCA[A/G]TTTCTCCATATCCTT | 8816 |
rs750706117 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146610 | CATAAGGTAGAGGGG[A/C]TATCTTTTAAAAGGT | 8816 |
rs750724041 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132051 | TCATCCACTGATGGA[-/C]CCTTGGGTTGCTTCT | 8816 |
rs750737328 | snp | C/T | 4.94417e-05 | 0.00497176 | missense | DCAF5 | GRCh38.p7 | 14:69055473 | GGACCGACTGGTTGG[C/T]GTAGTCATGCGACAG | 8816 |
rs750768411 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137913 | TAAATTAAATTTTAC[C/T]ATAGGTATGTATACA | 8816 |
rs750776789 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69115789 | AACACATGAGGTCCT[C/G]AACACCACAGTGCAA | 8816 |
rs750795250 | snp | A/T | 6.60786e-05 | 0.0057476 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69119214 | AACATCATGGAGGAT[A/T]ACTTGCTCATCATTG | 8816 |
rs750819890 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137083 | TCCTATAATTAATAC[A/G]TAATAGTTGTTTAAA | 8816 |
rs750822711 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104607 | ACGTCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 8816 |
rs750860533 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136592 | ATGTTTTTTCACTTA[-/T]GAAAACTAATATTTT | 8816 |
rs750864481 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082139 | CTATTTCCAGAAAAA[A/G]GTTTGCTAACTGGCA | 8816 |
rs750874028 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111489 | TCAAAGCAAGACACT[A/G]TTATCTGTCATAGAA | 8816 |
rs750874153 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125435 | TGCAAAGAATTTCTA[A/C]AAATAATTCTTAAAA | 8816 |
rs750926448 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054854 | TCATAGTTGTCTTCT[C/G]CAATGTAAGTGTTGG | 8816 |
rs750962070 | in-del | -/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052602 | TCTCTTCTAAACCTG[-/T]TATCTACCTCAATAA | 8816 |
rs751003825 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142408 | ACTGAGTCCAAGACC[A/G]GAACCAATGGAGCAA | 8816 |
rs751031472 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088654 | TTCTCATCCATGTTC[A/T]TTCCTATTACGGAAA | 8816 |
rs751062441 | snp | A/T | 3.33283e-05 | 0.00408204 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122406 | AACAGCTGACATCGC[A/T]AGGCTGACAGATGGT | 8816 |
rs751078904 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69092126 | TTACCAGTAAAGTTA[C/T]AAGAAAAGGATAACA | 8816 |
rs751137235 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065285 | TATTTTCAGTAGAGA[C/T]GGGGTTTCACCATCT | 8816 |
rs751140942 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140932 | CTCTGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 8816 |
rs751152104 | snp | C/T | 4.94931e-05 | 0.00497434 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122281 | GTTGGAATGGTGCTC[C/T]CCTTTCAGCTGTATG | 8816 |
rs751152443 | snp | C/T | 1.65616e-05 | 0.00287759 | missense | DCAF5 | GRCh38.p7 | 14:69053918 | TCTTCCAATTCAATT[C/T]GTTGCCTTTTGAGGC | 8816 |
rs751202571 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128842 | CCAGCACTTAGGGAG[A/G]TCGAGGTGGGAGGAT | 8816 |
rs751287115 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114147 | GATTTGTAAGTTAGT[A/G]CAGCCTTTGGTGGTG | 8816 |
rs751288417 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130303 | ATCAACAGAAGTCTG[G/T]TTAAAATTATTGTTT | 8816 |
rs751327399 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085248 | CTTTGTTGATCTGAA[C/T]GTCAACAGCAATGAA | 8816 |
rs751435435 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091743 | ACCCTGATTGTCAAA[C/T]TGAAACACAGGCAGG | 8816 |
rs751453207 | snp | A/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090261 | CTGTATATCTGTTCT[A/T]TTGAGAGTCTGATCG | 8816 |
rs751468094 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108016 | GCAGCTCCTGGGCAC[G/T]GGGAAGGAAATCAAA | 8816 |
rs751488973 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106556 | TTAAAAGAATACTTT[C/T]GTAGAGATAGGGTGT | 8816 |
rs751549734 | snp | C/T | 0.000115646 | 0.00760327 | missense | DCAF5 | GRCh38.p7 | 14:69054381 | GGTGCTCTACAGAGC[C/T]GCTATTGCCAGTGTC | 8816 |
rs751610440 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056620 | CAGGCAATCTTCTTG[A/C]CTGACAGGCTGGTGT | 8816 |
rs751612536 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071478 | GCTGACTGCTTGTCA[C/T]CTAGAGTCTAGTTCT | 8816 |
rs751644485 | in-del | -/GGCCAACATG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148504 | GTTTGAGACCAGCCT[-/GGCCAACATG]GTGAAACCCCGTTTC | 8816 |
rs751690218 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116602 | CTCTTTAATAACCAC[C/T]CCAACGGCCTGGAGC | 8816 |
rs751721781 | in-del | -/TTTTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067338 | AGCCGATTTCGTATC[-/TTTTTTTTTTT]TTTTTTTTTTTTTGA | 8816 |
rs751794810 | snp | A/G | 1.65157e-05 | 0.0028736 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119184 | CTTCACACACCACCA[A/G]TCTATTTACCTTTCA | 8816 |
rs751809930 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055261 | GGCGTTGTCGGCAGA[C/T]TCATCTACTGTGGGA | 8816 |
rs751843809 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060989 | TCAGGTTTTCAAAGT[C/G]ATTTTAATAAAAAAA | 8816 |
rs751846682 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111240 | TCTGGTCTCTATAGA[A/G]GTAGGATTGGCCCAG | 8816 |
rs751943641 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122542 | GGCACGTGTTCTCTA[A/G]GCCATTCATCTCTCC | 8816 |
rs751945654 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078890 | TTTTTTTTTTGAGAC[-/AG]AGTTTCTGCCGCCCA | 8816 |
rs751965475 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101405 | TTCAAAGATGTTACC[A/G]TTTCCATGAACAGTG | 8816 |
rs751970272 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137949 | CAAAACATAGTATAC[A/T]TAGGGTTCAGTACCA | 8816 |
rs751973207 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066285 | GATTACAGGCGCACA[C/T]CACCACGCCCAGCTA | 8816 |
rs751974467 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087477 | CTTTAAACAAAAAAA[C/G]TAAAAAAGTGTAAGC | 8816 |
rs751989378 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148428 | CGGGCTGGGTGGGGT[A/G]GCTCACACCTGTAAT | 8816 |
rs752001858 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075818 | TATATCTATCTGTAC[-/A]GAGATTTCCTTTAAA | 8816 |
rs752007465 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137720 | GTACAGTAAGCCCCT[C/T]TGCCCATGATTTCAC | 8816 |
rs752023746 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053514 | TTATGAGACAATAAG[C/T]GCACACGTGCCATTG | 8816 |
rs752043121 | in-del | -/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091017 | CTTCAGAACTTCTAT[-/G]GTTAAGACAGAAAGG | 8816 |
rs752078468 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057489 | ACTCACAACTAGTTA[A/T]CTAAAGTACAAAATA | 8816 |
rs752081481 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136927 | TTACAAAATACCAGA[A/G]GTGGCCTACTTTCAA | 8816 |
rs752113404 | in-del | -/GG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121185 | TTAGACTTCATTCTT[-/GG]CAGGCACTGTAGGCT | 8816 |
rs752119118 | snp | C/T | 1.6517e-05 | 0.00287372 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054631 | ATCTGCCTCCCCGGT[C/T]ACCAAGGAGGTCTCT | 8816 |
rs752129524 | snp | C/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154188 | TACAGTTAAAAGTCC[C/T]CTTTTCGATGTATTA | 8816 |
rs752152802 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086736 | GTCAACCCAGAGAGG[C/T]TGAGTGGTGATGTAA | 8816 |
rs752164028 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102700 | TCTACTAACATCTTC[A/G]GGGTCGATAATACAC | 8816 |
rs752194295 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106439 | AGTGGTGCAATCATG[G/T]CTCACTGCAGCCTCA | 8816 |
rs752215929 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119233 | TGCTCATCATTGCCT[A/G]CAAAAGAAAAAAGCA | 8816 |
rs752237448 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139551 | GGGCATGGTGCCTCA[A/T]ATCTGTAATCCCAGT | 8816 |
rs752260026 | in-del | -/TGTA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130582 | TGGTAAATCTTATGT[-/TGTA]TGTATACATTTCACA | 8816 |
rs752261594 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054868 | TCCAATGTAAGTGTT[C/G]GTGGGCTTGATTGGG | 8816 |
rs752271428 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056328 | AGGTAGGACACATGC[C/T]CCAAGGACAGGTAAC | 8816 |
rs752295228 | snp | C/T | 1.64737e-05 | 0.00286994 | missense | DCAF5 | GRCh38.p7 | 14:69054782 | AGCGTGGAAGTGCTC[C/T]GCTCAGGGGACGAGG | 8816 |
rs752327714 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127212 | CAACAGCTTTATTTA[C/T]AATTGCCAAAACTTA | 8816 |
rs752338445 | snp | C/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090090 | TATTAATATCACCTT[C/T]ACTGCATGCTCTATT | 8816 |
rs752350895 | snp | A/G | 4.69384e-05 | 0.00484428 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091890 | GCGCAGGAGAGAACT[A/G]GAAGGCACAAGGCAC | 8816 |
rs752417276 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125821 | AGCAAGTTTCGAAAG[A/G]ATATGAAAGGGATAA | 8816 |
rs752433540 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140652 | ACAAAAAAAAGTACA[A/G]GTAAACAGTATAATA | 8816 |
rs752436328 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096793 | TGGCTTATTCAAAAA[C/T]GCCCTCTACCCAAAA | 8816 |
rs752437362 | snp | A/G | 3.88734e-05 | 0.00440854 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091134 | AAACTCACAGCTTGG[A/G]CTCTCCATTTCCAGT | 8816 |
rs752495507 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145312 | TGTGAGCTACTGCAC[C/T]TGGCCTTAATTTACT | 8816 |
rs752541984 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082966 | AGAACTGCCATGTCC[C/T]GTCACCAGATTACAT | 8816 |
rs752573610 | snp | C/T | 3.75735e-05 | 0.00433421 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153005 | CGCCGCCGCCGCTCG[C/T]GCCGCCGCCCCTCCC | 8816 |
rs752614617 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071065 | AGCCTCCCAAAGTGC[C/T]GGGATTATAGGCATG | 8816 |
rs752636779 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068338 | TAAAGTTATCTGCTA[A/G]AATGAGGTTTGGTAA | 8816 |
rs752643054 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152059 | CTCGCAAGTTGCGCA[A/T]TCAAGTTCAGGCTGG | 8816 |
rs752654388 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069767 | GGTACGAGCCATTGT[A/G]CCTAGCAGCAGTTAG | 8816 |
rs752658319 | snp | C/G | 0.000115566 | 0.00760063 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118260 | ATCTTCATGAGCAAA[C/G]ACGTCCAATGTCTCA | 8816 |
rs752693782 | snp | C/G | 3.30398e-05 | 0.00406434 | missense | DCAF5 | GRCh38.p7 | 14:69055247 | GGCCCCAGGTGGAAG[C/G]CGTTGTCGGCAGACT | 8816 |
rs752697970 | in-del | -/TTGAAAGAT | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154349 | TGAGTAGAATCATCA[-/TTGAAAGAT]GGGCTGTACATCTCT | 8816 |
rs752710014 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121629 | TATTGTATTTAAGTT[A/G]CTTTTGGAACACAGG | 8816 |
rs752783676 | snp | A/C/G | 4.95203e-05 | 0.00497575 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118256 | CTGCATCTTCATGAG[A/C/G]AAACACGTCCAATGT | 8816 |
rs752791708 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123855 | AGGCTCCCACCACCA[C/T]GCCCAGCTAATTTTT | 8816 |
rs752835965 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149079 | AAGAAAACAAACTCA[A/G]TATTTTCTCTGAGAG | 8816 |
rs752854634 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052527 | TTCCCAGACCTTCCT[A/G]TTTTGCACAACCCTT | 8816 |
rs752862293 | in-del | -/TG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081755 | CCTTTATAGAAAATG[-/TG]TGTGTGTGTGTATGT | 8816 |
rs752888814 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075156 | AAGCATCATTTATGT[C/G]AGATAAGACTATGTC | 8816 |
rs752977114 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073531 | AGTGGCTCATGCCTA[C/T]ACGCCCAGCACTTTG | 8816 |
rs752992657 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122472 | CACCTCCCCAACTCC[A/G]TAAGATTCGCATGGA | 8816 |
rs752997679 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056667 | TCCAACCCAGAAAAC[A/G]GTGGCCCCTCAATTC | 8816 |
rs753010198 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108325 | TTACCATTTGATCTT[C/G]GTAACTATGACATGA | 8816 |
rs753036083 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147255 | TCACCTCATGGAGAT[A/C]TTTCTCAATATTTCA | 8816 |
rs753044547 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138615 | GAAAAGGTCAGAAGA[A/C]CCAGAGTTTAATCCT | 8816 |
rs753057489 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | DCAF5 | GRCh38.p7 | 14:69054540 | GGTTCCTCTGGGCCA[C/T]TGCTATGTTTAGACA | 8816 |
rs753066642 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142263 | CGTAACTGCCCCTGC[A/G]CTCTGGTCTGAGCAA | 8816 |
rs753070645 | snp | C/G/T | 6.6055e-05 | 0.00574663 | missense | DCAF5 | GRCh38.p7 | 14:69054627 | CTTCATCTGCCTCCC[C/G/T]GGTCACCAAGGAGGT | 8816 |
rs753082395 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134924 | ATTCACACCCATTGA[C/T]TCAGAATTCCACTTC | 8816 |
rs753096275 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101215 | AGATGGATTATTCCA[C/T]CTATTAAAAAGAACA | 8816 |
rs753130586 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064370 | GTGGTTAAGCAAAGA[A/T]ACTTTGATTTAAATC | 8816 |
rs753167758 | snp | A/G | 1.6549e-05 | 0.0028765 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69075409 | AGAGCCCGAAAGGAT[A/G]TACTGTTGGAACAAA | 8816 |
rs753172486 | in-del | -/G | 1.70895e-05 | 0.00292309 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091638 | ATCAGAAAGAAAAGC[-/G]ATAAGTGTGAGATGC | 8816 |
rs753232686 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066650 | CCAGGATCCCAGGGG[-/A]AAACACCTTGCTCAA | 8816 |
rs753235162 | snp | A/G | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050874 | AAAGAAATAAAGGAG[A/G]GGTGTCTAAGCAACC | 8816 |
rs753259649 | snp | A/G | 1.65721e-05 | 0.0028785 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062543 | AAACAAAAATCAGAT[A/G]ATGAAATGAATGAAA | 8816 |
rs753268260 | in-del | -/TC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133979 | TAACCCTAGACAATG[-/TC]TCTAATTCCTGATCA | 8816 |
rs753287148 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099921 | GTCTCAAAGAATAAA[A/G]TAACATTAAAAAAAA | 8816 |
rs753326296 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065250 | TACAGGCATCCACCA[C/T]CATGCCCAGCTAATT | 8816 |
rs753330831 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117771 | TTCGGTGGTTCTTTC[A/C]ACAAAATAACAAGCC | 8816 |
rs753356287 | snp | A/G | 1.65198e-05 | 0.00287395 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054649 | CAAGGAGGTCTCTCC[A/G]TCTTTGTTATTTGAG | 8816 |
rs753382690 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69089009 | TTAAAAAAAACTATA[A/G]GTTCAGTAGATTAGT | 8816 |
rs753387027 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103102 | TTGACTGAAACATCA[C/T]TATGCAGAACACACG | 8816 |
rs753406669 | in-del | -/TGTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108390 | CATCCTCTATGTGTA[-/TGTG]TTTTGGGGGGTGGTG | 8816 |
rs753450018 | snp | C/T | 3.70302e-05 | 0.00430276 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075436 | CAAAAAATATATAGA[C/T]AACATTATATATTAT | 8816 |
rs753458967 | snp | C/T | 6.81477e-05 | 0.00583688 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091104 | CCATTCCTGGTGAGA[C/T]TCAGAAAAGGCTGGA | 8816 |
rs753462337 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138126 | ATAGTCAAGACACCT[A/C]TTTAAAAAAAAAAAA | 8816 |
rs753479962 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139343 | TTAAAAATTAGCTGG[A/T]CGTGGTGATGCACAC | 8816 |
rs753490068 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104504 | AGCATAAGCTAGAAT[A/G]TAAGAAATTCGTAAG | 8816 |
rs753504955 | snp | C/G | 0.000119117 | 0.0077165 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152982 | TCTCCTCTTCATGCT[C/G]GAACCGCCGCCGCCG | 8816 |
rs753544260 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | DCAF5 | GRCh38.p7 | 14:69054151 | GTTCTGCCCGTTATT[G/T]TGAGGGTGAGGGGGA | 8816 |
rs753558444 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | DCAF5 | GRCh38.p7 | 14:69054953 | TGCCAGGTAGAGGCT[C/T]GGCGTTCATTCAGCT | 8816 |
rs753563367 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058677 | CCCAGGAATTTGAGA[-/C]CAATCTGGACAACAT | 8816 |
rs753571866 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152280 | CGGCCCCTCGGCGTC[A/C]GGGTCTGTCACCGCC | 8816 |
rs753593107 | snp | G/T | 1.67105e-05 | 0.0028905 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152897 | AGTCCTGAGTGAGCA[G/T]GGGGTCCCCATGCAA | 8816 |
rs753622015 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119706 | AGAGAGACTGTCTCA[-/A]AAAAAAAAAAAAAGT | 8816 |
rs753624863 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151559 | AGGGACAGAAGAGGG[A/C]AGCAGCCAAGCAGGA | 8816 |
rs753677232 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111149 | GGGCTTTATTTTCCT[A/G]TAATGGTATGAGCAA | 8816 |
rs753719166 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116687 | TCCTATACATAGCAA[C/G]GTAAACACATTTAAC | 8816 |
rs753721087 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132138 | GAGCCTCTACTTTCA[A/C]TTCTTTTGGGTATAT | 8816 |
rs753727259 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124272 | TTGGCTATTGTGAAT[A/G]ATGTTGCTATGAACA | 8816 |
rs753742263 | snp | C/G | 1.65252e-05 | 0.00287443 | missense | DCAF5 | GRCh38.p7 | 14:69055239 | CCCGCAGGGGCCCCA[C/G]GTGGAAGGCGTTGTC | 8816 |
rs753742311 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074296 | TATTGAGCTGTTTGA[A/G]TATTAAAAACAGACA | 8816 |
rs753771349 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082867 | AGGAGGAGGATGAGA[C/T]AGGTTATACTCTGTT | 8816 |
rs753813861 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131759 | AAGCACTTTCCAGGC[-/T]TTTTTTTTTTTTTTT | 8816 |
rs753833104 | snp | A/C | 1.6492e-05 | 0.00287154 | missense | DCAF5 | GRCh38.p7 | 14:69055143 | GGTAGCGCCGCAGAG[A/C]AGACAGACGCTGCTG | 8816 |
rs753875610 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095942 | ATCAGAGCTGGTGTC[A/G]TATCCCAAGTAGAGA | 8816 |
rs753919921 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148244 | AACCCAAGATATCCC[C/T]TAAATATGCGTACTA | 8816 |
rs753922130 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146776 | CACTAATAAATAGAT[A/C]AAATAATAAAATACC | 8816 |
rs753923831 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088029 | ACATAAAAATCTTTA[C/T]TTCTGTCCTCTCTTG | 8816 |
rs753924796 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116480 | GCTGATGGATAGTTT[A/G]CCAGGCAGAAGGGCT | 8816 |
rs753930687 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091510 | CATTGACAGCCTTGA[G/T]AAAGAAACTCACTAT | 8816 |
rs753947601 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133167 | AAGTAGGAATTCACA[A/T]GAAACTACAGAAAAG | 8816 |
rs753949162 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060298 | GGGAAGAACAAAGGG[A/C]AGGGCTCTATCCTAG | 8816 |
rs754006762 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056747 | ACAAATGCACCTCCC[C/T]GTGGGAATTCTCCTG | 8816 |
rs754052460 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086619 | GCGTGCATGGAGTTA[-/T]TAAAAAAAAAAAAAA | 8816 |
rs754059616 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071949 | AAAACCATGCACATG[A/G]CCAGGAAACCATCCT | 8816 |
rs754089647 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054520 | GCCTTCAGGTGGCAG[A/G]TCCTGGTTCCTCTGG | 8816 |
rs754092099 | in-del | -/C | 1.64906e-05 | 0.00287142 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122207 | CCCAAGGTAGAATCT[-/C]CCTTTTTACCTCCAG | 8816 |
rs754118396 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085604 | TTGGTTGCCCAAGGG[C/T]AAAGTAAGGAATATC | 8816 |
rs754140503 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094537 | ACACTGAAAACTTCA[-/T]GTTTTGTCACAAAAT | 8816 |
rs754144636 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120568 | AATTAAAACCTGAAT[A/G]TAAGAAGACAAAACA | 8816 |
rs754167498 | in-del | -/AAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148103 | GTTCATTTTCTTCGC[-/AAA]AAAAAAAAAAAAAAA | 8816 |
rs754177811 | snp | A/C | 1.65064e-05 | 0.00287279 | missense | DCAF5 | GRCh38.p7 | 14:69054417 | AGGTACCCTCTGGCA[A/C]CTCTGCCCAAGCATG | 8816 |
rs754205121 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062510 | CACCCTACCAATGCC[A/G]CCTGGGAAAACAGAA | 8816 |
rs754219346 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125582 | TAGACAGATTCTCAC[A/G]AAGTGGCACAAGGGA | 8816 |
rs754243997 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115068 | TGCCTTTTGTAATAC[A/G]GATGAGGCAGAACAG | 8816 |
rs754252473 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113505 | GTTATAGGGGATTCA[C/T]AAATTCCTTAAAATC | 8816 |
rs754259173 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076684 | GGGATGATGAAGAAG[C/T]TCTGAAGGTAGATAG | 8816 |
rs754290015 | in-del | -/ATATT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137839 | TTTTATTACAGTATA[-/ATATT]ATAATTGTTCTACTT | 8816 |
rs754294374 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097145 | AAAAAATCCTAAGCA[C/G]AAGAGGGTTTGAAAA | 8816 |
rs754296798 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112854 | ATGCCTATTAAGGTG[C/T]ACTACCTGGATCTGT | 8816 |
rs754319614 | snp | A/C | 0.000247266 | 0.0111163 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122233 | TCCAGAGAACACTTT[A/C]GTGTTCCCACTGTTG | 8816 |
rs754319970 | snp | G/T | 1.67027e-05 | 0.00288982 | missense | DCAF5 | GRCh38.p7 | 14:69053891 | TCTGAGGAGGAATTC[G/T]CTGAATCTGTATCTT | 8816 |
rs754346541 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127098 | CATACAAAACTAAAC[A/G]TACTCTTATCACGCA | 8816 |
rs754367121 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064165 | GAGAGAATTAGGGAA[A/G]AGGGATAAATAGGAA | 8816 |
rs754375826 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081796 | TGGTGCGTGCTTACA[A/C]AGGATTTGATCTTCT | 8816 |
rs754386322 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112709 | TACCTCATAGGGTTA[C/T]CATAAGGATTAAATG | 8816 |
rs754415862 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087861 | AGTTAGTGACAGACC[A/G]TGGCACTAAACATGA | 8816 |
rs754433826 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141140 | CTCCATCTCAAATTT[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAAGTG | 8816 |
rs754455309 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063171 | AGAGTGGGCCTTAAA[A/G]ATACCATGTATAGAT | 8816 |
rs754469450 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138171 | CTCAAAGGTTCCAAT[C/T]AGTCACTTAGCTTTA | 8816 |
rs754505937 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103214 | GTGAAAAACATAGAA[A/G]CATATGGAAATAATG | 8816 |
rs754553549 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151046 | CTGGGAACTTCTCTG[C/T]TGTAATACATCGGGA | 8816 |
rs754597175 | snp | G/T | 3.40663e-05 | 0.00412698 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091105 | CATTCCTGGTGAGAC[G/T]CAGAAAAGGCTGGAA | 8816 |
rs754629419 | snp | C/T | 1.65201e-05 | 0.00287398 | missense | DCAF5 | GRCh38.p7 | 14:69054656 | GTCTCTCCATCTTTG[C/T]TATTTGAGTAGGAGA | 8816 |
rs754642589 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093156 | TACAGAGGGATGACT[C/G]CTCATAGTCCATGTC | 8816 |
rs754657998 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124292 | TGCTATGAACACAAG[C/T]GTACAAATAACTTTT | 8816 |
rs754719365 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130321 | AAAATTATTGTTTAA[C/T]AAAATAAGCCAGACA | 8816 |
rs754721538 | snp | A/T | 9.28225e-05 | 0.00681195 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075440 | AAATATATAGATAAC[A/T]TTATATATTATAATA | 8816 |
rs754723895 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130522 | ATTAATTACATGAAT[A/G]TAATTAATACCACTG | 8816 |
rs754772617 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081607 | AGCATAGGAAGAGAT[C/T]AACAACTCTCTCTCA | 8816 |
rs754775232 | snp | G/T | 1.67206e-05 | 0.00289137 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152899 | TCCTGAGTGAGCAGG[G/T]GGTCCCCATGCAAGC | 8816 |
rs754810044 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129280 | CCTCAAGGTTAGCAT[C/T]AGAAGATGTAAGCTA | 8816 |
rs754846834 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053216 | AAATTCTTTTTTATA[G/T]TATGTCCACATTAAA | 8816 |
rs754848119 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143860 | CATTTTTTTATGACT[A/G]GTCAAGTGAAGCAAT | 8816 |
rs754862962 | snp | A/G | 2.58468e-05 | 0.00359482 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152740 | GGTGCGGGGAGGCGC[A/G]GGGAGGGGAAGGGGG | 8816 |
rs754876261 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094535 | CAACACTGAAAACTT[C/G]ATGTTTTGTCACAAA | 8816 |
rs754918067 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116835 | TCCACATGAGCTGAA[A/C]AAATTCACAACCAAG | 8816 |
rs754934562 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149560 | TTTACCCAGCCACAG[A/G]AATCATGCAAATATT | 8816 |
rs754961000 | snp | A/G | 3.30491e-05 | 0.00406491 | missense | DCAF5 | GRCh38.p7 | 14:69054036 | CCATTTCAGACCCGC[A/G]ACAATCTTTGTGTAG | 8816 |
rs755048876 | snp | A/C | 1.64947e-05 | 0.00287177 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055147 | GCGCCGCAGAGCAGA[A/C]AGACGCTGCTGGCGA | 8816 |
rs755061176 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120589 | AGACAAAACATGAAA[A/G]AAGTCCCACTCTATG | 8816 |
rs755062069 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070182 | GTAGCTCTGGAAAAG[C/G]AACTCAACCTGTGAA | 8816 |
rs755117674 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084349 | CCCAGGGTTTATGTA[C/T]AAAAATCTGCAGTGT | 8816 |
rs755120920 | snp | A/T | 3.30502e-05 | 0.00406497 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116502 | AGAAGGGCTCTGTGG[A/T]AAGAAAAATTATAAT | 8816 |
rs755127404 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133368 | TGAAGAATATATCTG[A/T]ATTTTTAAAAGATAA | 8816 |
rs755138275 | snp | A/G | 1.67153e-05 | 0.00289091 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116331 | AGAAATGAGGCAGAG[A/G]AAAGTTTTAACACCT | 8816 |
rs755142921 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120955 | ACATGGAGAAGGAGA[C/T]CTTTGAAGAGAAACT | 8816 |
rs755143053 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | DCAF5 | GRCh38.p7 | 14:69055041 | TGGGTGACCGTGGCC[A/G]GGGAAAGAGATCTGT | 8816 |
rs755230343 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | DCAF5 | GRCh38.p7 | 14:69054526 | AGGTGGCAGGTCCTG[C/G]TTCCTCTGGGCCATT | 8816 |
rs755238501 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145939 | TCTTTGCCTTGATCA[A/G]TGCATGAGAAAATAA | 8816 |
rs755255658 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107317 | TGGGTCTGAGTGAAC[G/T]TGAGCAAATTCAACA | 8816 |
rs755289842 | in-del | -/AG | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052679 | CAGGAGTCATAAGCC[-/AG]AGACTCCTCCCCAAC | 8816 |
rs755351194 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125644 | ATAATATCAAGAAAA[C/T]CTATATACAACATAA | 8816 |
rs755374050 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063204 | AAGTCAAGAGGACAT[C/T]GATAGAAAGCTGTAT | 8816 |
rs755374092 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078123 | AAGACAAGGAAACTC[A/G]TAAGGCCAGTCTTGT | 8816 |
rs755409938 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152390 | GCCTCCTCACCCTCC[A/C]CATCCCCAAAATGCC | 8816 |
rs755423562 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111614 | TAGAGTGAGAGCAGG[A/G]GAAACTTTTGCTTTT | 8816 |
rs755461889 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076693 | AAGAAGTTCTGAAGG[C/T]AGATAGTGGTGATGG | 8816 |
rs755476918 | snp | G/T | 3.31203e-05 | 0.00406928 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062342 | TTCTAATTATAAATT[G/T]TGAGAATTTCTCTAA | 8816 |
rs755504211 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146948 | TGATAAGTAACTACC[A/G]AACCAACAAATTCAT | 8816 |
rs755543458 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101618 | AATACAGTCATGCAT[C/T]GCTTAATGACAGGAA | 8816 |
rs755575163 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064193 | GAATCTAAAGAACCC[A/C]AAAATAGTTGTCTTG | 8816 |
rs755596230 | snp | C/G/T | 3.29735e-05 | 0.00406028 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122243 | ACTTTAGTGTTCCCA[C/G/T]TGTTGAAAGCCAGGC | 8816 |
rs755607422 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066434 | GCCACTGCACCTGGC[C/T]AGCTGACACTCCTTT | 8816 |
rs755611119 | snp | A/C/T | 3.42743e-05 | 0.00413959 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075432 | GGAACAAAAAATATA[A/C/T]AGATAACATTATATA | 8816 |
rs755631495 | snp | C/T | 4.9552e-05 | 0.0049773 | missense | DCAF5 | GRCh38.p7 | 14:69054633 | CTGCCTCCCCGGTCA[C/T]CAAGGAGGTCTCTCC | 8816 |
rs755644268 | in-del | -/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097583 | TTATTATTATTATTA[-/TT]TTTTTTTTTTTTTTT | 8816 |
rs755719330 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | DCAF5 | GRCh38.p7 | 14:69054554 | ATTGCTATGTTTAGA[C/T]AGGCTTCCTTACTGG | 8816 |
rs755769804 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075301 | CATGCCAAAGGTCAA[C/T]AGAGCCAGCAATAGC | 8816 |
rs755777879 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137099 | TAATAGTTGTTTAAA[C/T]TATGAATGGGTGGGA | 8816 |
rs755801711 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053108 | CATACAGTACATGTT[C/G]CAGCACTGCTCAATT | 8816 |
rs755872623 | snp | C/T | 1.65375e-05 | 0.0028755 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054031 | ACAGGCCATTTCAGA[C/T]CCGCAACAATCTTTG | 8816 |
rs755886819 | snp | C/T | 1.65504e-05 | 0.00287662 | missense | DCAF5 | GRCh38.p7 | 14:69053949 | CACTGTGGCCATGAA[C/T]AGCCCTGCTACTATC | 8816 |
rs755924850 | snp | A/C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141102 | TCACGCCACTGCACT[A/C/T]CAGCCTGGGCCACAG | 8816 |
rs755925283 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059294 | TTCCCTGTGTTGTCC[C/T]TGACAATAGGGACTC | 8816 |
rs755933693 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068943 | ATGGGGACAGCCAAT[A/G]CTGTCAGTACAGCTC | 8816 |
rs755938112 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081471 | TGTGGTCCAAGAGGG[C/G]AAGCTATTTACTGAT | 8816 |
rs755974900 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | DCAF5 | GRCh38.p7 | 14:69055031 | TCTTCGGGGCTGGGT[A/G]ACCGTGGCCGGGGAA | 8816 |
rs756043451 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129038 | GGTCTCCCTCCATTA[C/G]CCAGACAGAAATAAT | 8816 |
rs756050295 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117300 | CACAGCTGCTACTTC[A/G]TGCTACCTTACCTGC | 8816 |
rs756084203 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086353 | ATAGAGCAAGACTCC[A/G]TCTAAAAACAAACAA | 8816 |
rs756089195 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107215 | AGATGCTCTGGTCTG[-/A]AAGCGACGTCTCTTG | 8816 |
rs756097863 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080186 | GATACATTTACTATC[A/C]TAAGAGCAGCTAGAA | 8816 |
rs756104741 | in-del | -/AT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058539 | AGAAAAAAAATACAT[-/AT]ATATATATATATGGC | 8816 |
rs756136297 | snp | A/T | 8.23608e-05 | 0.00641667 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054916 | TCGGGTTGTCTTCTG[A/T]CGGCGCCGCATGGCA | 8816 |
rs756152799 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124146 | GGTCGTGGCATGTAT[C/G]AGAATTTCCTTGCTT | 8816 |
rs756180692 | snp | A/G | 1.67556e-05 | 0.0028944 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091933 | TGAGATAGGCTAAAC[A/G]AGAGTCTGAAAAACA | 8816 |
rs756195238 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146716 | TTGTCCCTGTTCTCA[G/T]AGCTCCTGTTTTACA | 8816 |
rs756243946 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112477 | TGGTGGCTCATGCCT[A/G]TAATTCCATCTACTC | 8816 |
rs756257665 | in-del | -/A | 8.26426e-05 | 0.00642763 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116505 | GGGCTCTGTGGAAAG[-/A]AAAAATTATAATCAG | 8816 |
rs756266924 | snp | A/G | 3.33667e-05 | 0.00408439 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091827 | CTGGGTCCCGTTGCT[A/G]TTGAATCGTACACTC | 8816 |
rs756279558 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096249 | TTTCTCTTTTGTTTT[C/T]CTAATGCACTCCTCA | 8816 |
rs756284308 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118497 | AGATTTTATAATTTT[A/T]GTGCTAAATAAGCAT | 8816 |
rs756325735 | snp | C/T | 1.6519e-05 | 0.00287388 | missense | DCAF5 | GRCh38.p7 | 14:69054393 | AGCCGCTATTGCCAG[C/T]GTCCTGAGAGGTACC | 8816 |
rs756412543 | in-del | -/G | 0.00156275 | 0.0279094 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053815 | AATTTTTTTTTTTTT[-/G]TAAGGCTACTTTTGT | 8816 |
rs756413465 | snp | C/G | 1.64966e-05 | 0.00287194 | missense | DCAF5 | GRCh38.p7 | 14:69054300 | ATGCCTTGGGGACAG[C/G]AGGAGAAGGCGGCTC | 8816 |
rs756415580 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105544 | TGGGCAGGGAGAACA[C/T]GACCCGCCTTTAATG | 8816 |
rs756417324 | snp | A/G | 1.75053e-05 | 0.00295844 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055639 | TGAAAAACAAAAGCA[A/G]CAAGGAGTAACTGGA | 8816 |
rs756433331 | in-del | -/ATA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137836 | AACTTTTATTACAGT[-/ATA]ATATTATAATTGTTC | 8816 |
rs756448528 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079936 | GGGGGTTGGGGTGTT[-/A]AGTTTCCGTTTTACA | 8816 |
rs756451821 | in-del | -/A | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051065 | ATCAAGCATAGTCAC[-/A]AACTTCACTTGCCCC | 8816 |
rs756484253 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137915 | AATTAAATTTTACCA[C/T]AGGTATGTATACATA | 8816 |
rs756511733 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123129 | TGATAGCACATCCAT[A/C]CAAGGGCATACTATG | 8816 |
rs756522426 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075741 | CGCTGGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 8816 |
rs756609211 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061492 | GGCTAGGACCCACTT[C/T]TGCAGTTATAAAAAC | 8816 |
rs756616133 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087700 | ACCATCTGGCAATGT[C/T]ATGTGAATGTATCTA | 8816 |
rs756619733 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111526 | GTTCCTGACAGAAAA[C/T]AAAGAGATTGGAAGG | 8816 |
rs756647710 | snp | C/G | 3.31285e-05 | 0.00406978 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118285 | GTCTCACTGCTGGGA[C/G]ATAAGAGAGCAAGAC | 8816 |
rs756742268 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128848 | CTTAGGGAGGTCGAG[A/G]TGGGAGGATCCGTAA | 8816 |
rs756777607 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114162 | ACAGCCTTTGGTGGT[A/G]GGGCTACAATTTGAC | 8816 |
rs756782567 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118350 | GTCCCAGCACTTTGG[G/T]ACCGAGGGTGCCATC | 8816 |
rs756800949 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066363 | GCTGGTCTCCAACTC[C/T]TGACCTCATAATCTG | 8816 |
rs756857703 | snp | A/G | 6.59609e-05 | 0.00574248 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062387 | AAGGTGCCTCACCTT[A/G]ATAATCTTTTCTACA | 8816 |
rs756859297 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104670 | AGACCAGCCTGGCCA[A/T]CATGGTGAAACCCCA | 8816 |
rs756875615 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051301 | GGAAGAAATTGGGTA[C/T]TAAATGTGCCATCAA | 8816 |
rs756901508 | snp | A/G | 1.65408e-05 | 0.00287578 | missense | DCAF5 | GRCh38.p7 | 14:69053940 | TTTTGAGGCCACTGT[A/G]GCCATGAACAGCCCT | 8816 |
rs756906017 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148437 | TGGGGTGGCTCACAC[C/T]TGTAATCCCAGGACT | 8816 |
rs756945340 | snp | C/T | 3.29962e-05 | 0.00406165 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122284 | GGAATGGTGCTCTCC[C/T]TTCAGCTGTATGGGC | 8816 |
rs756961343 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065294 | TAGAGACGGGGTTTC[A/G]CCATCTTAGCCAGGC | 8816 |
rs756972988 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152496 | CGACCTACACTTTCA[C/G]GGCAGGCATCAGGAG | 8816 |
rs756989185 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154224 | CTTTTCCTGGAAGCT[A/G]TCCTCTGTCATTAAG | 8816 |
rs757020700 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | DCAF5 | GRCh38.p7 | 14:69054960 | TAGAGGCTCGGCGTT[C/T]ATTCAGCTCCTCCTC | 8816 |
rs757020730 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139994 | AGACAGAGAGGCCAG[G/T]CGCAGTGGCTCACAC | 8816 |
rs757059730 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071718 | GATTAAGAGTTTCCT[A/G]ACAAAATTTTCCTCA | 8816 |
rs757069802 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096076 | ATAATACAACCCACA[-/G]AATATGACAAATCCT | 8816 |
rs757075377 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153273 | CGCCGGCTGCGGGGC[C/T]CCGAGAACGCGGCGT | 8816 |
rs757104432 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056676 | GAAAACAGTGGCCCC[C/T]CAATTCCCCATCCTT | 8816 |
rs757111344 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091759 | TGAAACACAGGCAGG[A/C]GGGAATGGATGTCAT | 8816 |
rs757125363 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120293 | TCTAACATGTTGGGG[C/T]CTAACTATGTTGCCC | 8816 |
rs757158620 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108168 | ATGGAGAGATCCTTT[C/T]CTCTAGAAGTTAGGG | 8816 |
rs757184347 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095552 | TGTTTTTTTAAGTAC[-/AC]ACACACACACACAAA | 8816 |
rs757203993 | snp | A/C | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090270 | TGTTCTATTGAGAGT[A/C]TGATCGCCTATAGAA | 8816 |
rs757217719 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057098 | TAAGTCATGAACAGG[G/T]ATCAGGACCATGCAT | 8816 |
rs757262987 | in-del | -/T | 1.65638e-05 | 0.00287778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122373 | TCCTTAAGAAGGAAA[-/T]TAAGAATCTGTGCTT | 8816 |
rs757276544 | snp | A/G | 0.000151023 | 0.00868843 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091176 | CAGTAAAAAGAAAAA[A/G]AGTCAGCATCTGGCT | 8816 |
rs757300278 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057847 | TTCACTCCAGACACA[C/G]AGTACAGCACTTCAG | 8816 |
rs757312283 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061046 | GGTCTCACTCTGTTG[C/G]CTAGGCTGGAGTGCA | 8816 |
rs757317427 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094763 | GCTTCAAGTGTAAGA[C/T]GCATGAAAAATCATC | 8816 |
rs757372430 | in-del | -/CCTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079022 | CGGGCACCACCATTT[-/CCTG]TTACGTTACACGTTT | 8816 |
rs757376973 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123801 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8816 |
rs757382791 | snp | G/T | 1.64855e-05 | 0.00287097 | missense | DCAF5 | GRCh38.p7 | 14:69054267 | AGTTGCCAGACCCGC[G/T]GTTGAGAGTGGAGCC | 8816 |
rs757403286 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109729 | TCCATTTTCTTTTGA[C/T]GGATATTTAGGTTGT | 8816 |
rs757414844 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082759 | TCAAGCAAAGGTGTT[A/C]CAGCATTCTGAGGAA | 8816 |
rs757431257 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096116 | TAGAACTAGGTAAAA[A/C]GTCAGCAAGTTCAGG | 8816 |
rs757440664 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | DCAF5 | GRCh38.p7 | 14:69055446 | AGAAGGCCATCATCC[A/G]GGGGTCTTCCTGGAC | 8816 |
rs757535864 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086839 | GGGATGGGACAGGAT[A/G]ATTTTATGATCACGA | 8816 |
rs757553319 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075847 | AATAAACAAGATAAA[C/T]GGGCATATATTTATA | 8816 |
rs757557724 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136966 | TTAATGTATGTATAC[G/T]AAATGTGTATCAAAA | 8816 |
rs757586976 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149304 | TGCCTAACCCAGTAT[C/T]ACAGCGATGCCCCTT | 8816 |
rs757641308 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080254 | CCCCTCCTGGACTCA[A/G]GCTGGTTGGGGCCAC | 8816 |
rs757647461 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135266 | CGCTAGGGCAGTGAC[A/G]GCAAATTGTACTATT | 8816 |
rs757649437 | snp | A/G | 8.25812e-05 | 0.00642524 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118263 | TTCATGAGCAAACAC[A/G]TCCAATGTCTCACTG | 8816 |
rs757692370 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059677 | TACCACCTGCCTTCC[C/T]GCAATGCTTAGTGCC | 8816 |
rs757712316 | snp | A/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075612 | TCAACCTCCAGAGTA[A/G/T]CTGGGACTACAGGCA | 8816 |
rs757756050 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122826 | GATCTCATTGATTGT[G/T]GAACACCATACAAAT | 8816 |
rs757756546 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101436 | CTGTAATAAGGGGAA[A/G]ATCTGCCAAGAGAGG | 8816 |
rs757808571 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087503 | TAAGCCTTTAGTTAA[A/G]GCTAATTGCTTCTGT | 8816 |
rs757818067 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076923 | AGCAGGAAGCCATCA[C/G]CAACATAGCCATGAA | 8816 |
rs757861598 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140717 | GTAACATTAGCCTCT[C/G]GACCTGGCATGTTCA | 8816 |
rs757868427 | snp | C/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090101 | CCTTCACTGCATGCT[C/G]TATTATTCAACAAAA | 8816 |
rs757919747 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125836 | GATATGAAAGGGATA[A/G]TATCTAAGCATGTAT | 8816 |
rs757955772 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148104 | TTCATTTTCTTCGCA[-/AA]AAAAAAAAAAAAAAA | 8816 |
rs757989572 | snp | C/G | 1.65479e-05 | 0.0028764 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119251 | AAAGAAAAAAGCAGA[C/G]ATCTGATCATTCGTG | 8816 |
rs758004724 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064431 | CTCAAAAAGAGGGGG[G/T]ATGTGGGGGGATTTA | 8816 |
rs758041864 | snp | C/G | 3.29451e-05 | 0.00405851 | missense | DCAF5 | GRCh38.p7 | 14:69054872 | ATGTAAGTGTTGGTG[C/G]GCTTGATTGGGGCAC | 8816 |
rs758117270 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121732 | GTTGATGGAAGCCAT[-/CA]CACCAAGAGGTTGGT | 8816 |
rs758127961 | snp | A/G | 1.64974e-05 | 0.00287201 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091701 | TCCTGCAAAACAGCA[A/G]CTTTTCATGGTGCAT | 8816 |
rs758129860 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088357 | AAAGGTTTGTATAAA[A/G]TGATCTCTAATAGCT | 8816 |
rs758130008 | snp | A/G | 3.29473e-05 | 0.00405864 | missense | DCAF5 | GRCh38.p7 | 14:69054783 | GCGTGGAAGTGCTCC[A/G]CTCAGGGGACGAGGT | 8816 |
rs758162242 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118314 | ACAGAGGCACACACA[C/T]ACACACAAGCATAGT | 8816 |
rs758163575 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117122 | TAGCAGGATATACTC[A/C]TATGGGACCTGTTAG | 8816 |
rs758217942 | snp | C/G | 3.9447e-05 | 0.00444094 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091135 | AACTCACAGCTTGGG[C/G]TCTCCATTTCCAGTT | 8816 |
rs758239445 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152460 | TCAAACTTTGTAGAG[C/T]GGTAACCTCGCCCCC | 8816 |
rs758243240 | snp | C/T | 7.96052e-05 | 0.00630843 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153008 | CGCCGCCGCTCGCGC[C/T]GCCGCCCCTCCCTCG | 8816 |
rs758248841 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068359 | GGTTTGGTAAGTAGA[C/T]TTAAGACAATCTATT | 8816 |
rs758249042 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084053 | TGCAGCTACAAAAAC[C/T]GTCAGTGGTAAAACC | 8816 |
rs758332271 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104963 | CCTGCTTCACAAAAA[C/T]CATTGTAACAACTAG | 8816 |
rs758341478 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150705 | AGCCTGGGCAACATA[-/G]GGAGACTCCACCTCT | 8816 |
rs758355939 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122491 | GATTCGCATGGAGCA[C/T]AAAAACCCAGGACTC | 8816 |
rs758393709 | snp | C/T | 3.29989e-05 | 0.00406182 | missense | DCAF5 | GRCh38.p7 | 14:69055328 | TCAGTGTAGCCTGAG[C/T]GCTCGCTGACCCCAG | 8816 |
rs758424053 | snp | A/G | 1.69183e-05 | 0.00290841 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152930 | CCCGCTGGGACAAGA[A/G]GCCCACCACTGACCT | 8816 |
rs758482350 | snp | A/G | 3.29625e-05 | 0.00405958 | missense | DCAF5 | GRCh38.p7 | 14:69054162 | TATTGTGAGGGTGAG[A/G]GGGACGAGGGTGTAA | 8816 |
rs758494282 | in-del | -/TT | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053802 | GTATTCACTAAACAA[-/TT]TTTTTTTTTTTGTAA | 8816 |
rs758528270 | snp | A/G | 3.30322e-05 | 0.00406387 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055249 | CCCCAGGTGGAAGGC[A/G]TTGTCGGCAGACTCA | 8816 |
rs758541318 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072224 | AAGTCAACAGAGAAT[A/G]TCTAATATTGAAAAT | 8816 |
rs758542198 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143093 | ACATCTGCTTGAGAA[C/G]TAAGTACTGTGGCTG | 8816 |
rs758561423 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060620 | CACTACAACCTCCGC[A/G]TCCTGGGTTCAAGTG | 8816 |
rs758603243 | snp | A/T | 1.66178e-05 | 0.00288247 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116538 | CACTCCAGGTACCTG[A/T]GGGCCACTGGCAGGC | 8816 |
rs758649879 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099978 | GTTCAAAAGGAAAAT[C/T]ATTTAAGCTTTAAAA | 8816 |
rs758652534 | in-del | -/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089329 | ATATAAATCTCTGTA[-/T]TTTTATATACCTCTA | 8816 |
rs758654615 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059572 | CAAGGGTCGAGACTC[A/C]GCGGCCTTTCAGGAT | 8816 |
rs758659158 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148417 | AGTAATGTTAACGGG[A/C]TGGGTGGGGTGGCTC | 8816 |
rs758803274 | in-del | -/ATTTTATCTATTTTCAAGT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131779 | TTTTTTTTTTTAATG[-/ATTTTATCTATTTTCAAGT]ATAGAGTTTTGTGGC | 8816 |
rs758873923 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126219 | CTGGAGTGCAATGGC[A/G]CAATCTCAGCTCACT | 8816 |
rs758918160 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085870 | CTTCCTCACCAGACC[A/T]TATCATTGCTTGATC | 8816 |
rs758921756 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135100 | CATGCTTCAGAACAG[C/T]TGTTCTCGAAGTGTG | 8816 |
rs758975589 | snp | A/G | 2.06392e-05 | 0.00321235 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091872 | GGACAGGTTTCCACC[A/G]TAGCGCAGGAGAGAA | 8816 |
rs759017150 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054858 | AGTTGTCTTCTCCAA[A/T]GTAAGTGTTGGTGGG | 8816 |
rs759046828 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152322 | CCCAAGACCCCTTTT[C/T]CTTAACGCCGGCGAC | 8816 |
rs759064390 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057382 | TATTTGTAATTCTGA[A/G]CCAAATCTCTCACCT | 8816 |
rs759070470 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076417 | GATGAATGGATAAAC[-/A]AAAATGTGGTAATAC | 8816 |
rs759099778 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084835 | TACAGATGTGGCAGC[A/G]AGAGAACTGGACATT | 8816 |
rs759123697 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106226 | TACGCCCGGCTAATT[C/T]TGTATTTTTAATAGA | 8816 |
rs759189422 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145257 | TCCGGGGCTCAAGTG[A/T]TCCTCCTGCCTCTGC | 8816 |
rs759198589 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121309 | AGAAGGCCATTGCAA[A/C]AATCCAGGCCAAACT | 8816 |
rs759228720 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051609 | ATTTCTCTTTTGAGT[A/G]CCCAAATGAGATTAA | 8816 |
rs759236858 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134081 | TGTAAGGCACCTAAG[-/A]GTTCATCTTCTAACA | 8816 |
rs759247077 | snp | C/G | 2.41485e-05 | 0.00347472 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152983 | CTCCTCTTCATGCTG[C/G]AACCGCCGCCGCCGC | 8816 |
rs759247506 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154044 | TTAAAGGTCTCGAGT[A/G]GGGAGCACTGAGGTT | 8816 |
rs759272419 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054343 | GCTCAGGGCCTTTCC[A/G]TTGAGCTTCTTGGTT | 8816 |
rs759364365 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | DCAF5 | GRCh38.p7 | 14:69054216 | AGATGGTTTCGAGGC[C/T]CCTCTCCTCACTGTC | 8816 |
rs759428506 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111153 | TTTATTTTCCTATAA[C/T]GGTATGAGCAACCCT | 8816 |
rs759460233 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132156 | CTTTTGGGTATATAA[C/G]CAGAAGTGAAATTGC | 8816 |
rs759471837 | snp | A/G | 4.9525e-05 | 0.00497595 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118228 | TTCACTGGGCTCACA[A/G]ACAAGCCATATACTG | 8816 |
rs759476869 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083700 | AGCAGCAATGCAGTC[C/T]CCTAATTCAGAATCA | 8816 |
rs759476898 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098453 | ATTTTGTTTCCTATT[C/T]GTCTTTTCCCACTAG | 8816 |
rs759507825 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146395 | TAGCTGACTAAAGAA[C/G]CAAGTAGGACAAATA | 8816 |
rs759510274 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119146 | TATTTGCCTCTTCAT[A/G]TATGAAAAACAAAGT | 8816 |
rs759515128 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063731 | TATCTTCTGCTTTTG[A/G]CCCCCTAACACAACT | 8816 |
rs759531038 | snp | A/C | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050701 | AGAACAAATAAATAC[A/C]TCCTCCTACCCTGCA | 8816 |
rs759538384 | snp | G/T | 6.60982e-05 | 0.00574846 | missense | DCAF5 | GRCh38.p7 | 14:69055240 | CCGCAGGGGCCCCAG[G/T]TGGAAGGCGTTGTCG | 8816 |
rs759555257 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128495 | ATATTTCCATAATAA[-/AG]AGTTTTGGATTATGT | 8816 |
rs759564651 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096670 | GCCCCACAGAACCAA[A/T]CAAGATCTCAAAGCA | 8816 |
rs759571785 | snp | C/G | 3.29717e-05 | 0.00406015 | missense | DCAF5 | GRCh38.p7 | 14:69054737 | GATTCTATGTCAGAA[C/G]TTGGTGATGCCCGGC | 8816 |
rs759590165 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114728 | ACCAATAAATGTCAC[C/T]GTAAAAATACAATAA | 8816 |
rs759602008 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152022 | AACAAGTCTCCCGGG[G/T]GTCCCCCACCCTACC | 8816 |
rs759616458 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148925 | CCCAAGCACTTTCCA[C/T]ACCACATTGTGCCTC | 8816 |
rs759624774 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116154 | TACAGTCCAGATTAC[C/T]GTTTATGATTCCTCC | 8816 |
rs759646836 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102592 | TTGTTAAAAACAAAG[-/AC]ACACACACACACACA | 8816 |
rs759686731 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087319 | AGAATGTACCCAGTC[A/G]GGCTTCAGGGAGAAA | 8816 |
rs759687225 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065852 | TGGAAGGAGACAGGA[A/G]GGGCATATTTTTATC | 8816 |
rs759787399 | snp | C/T | 1.651e-05 | 0.0028731 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054622 | TCTCCCTTCATCTGC[C/T]TCCCCGGTCACCAAG | 8816 |
rs759835754 | snp | C/T | 1.65299e-05 | 0.00287483 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062521 | TGCCACCTGGGAAAA[C/T]AGAAGGAAACAAAAA | 8816 |
rs759888238 | in-del | -/ACACACAC/ACACACACACACACACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102593 | GTTAAAAACAAAGAC[-/ACACACAC/ACACACACACACACACAC]ACACACACACACACA | 8816 |
rs759906874 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080531 | AGTGAAATTGGAGGC[A/G]CAGGTTTTTCTCTCT | 8816 |
rs759908275 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127124 | ACGCAATCCAGCAAT[C/T]ATGCTCCTTGGTATT | 8816 |
rs759943384 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141982 | TCAACTCTGTATCCC[A/G]AGAGGTATATGATAG | 8816 |
rs759946947 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058474 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 8816 |
rs759975931 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126309 | ATTACAGACACCCAC[C/T]ACCACGCCCAGCTCA | 8816 |
rs759996494 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090098 | TCACCTTCACTGCAT[A/G]CTCTATTATTCAACA | 8816 |
rs759998729 | snp | A/G | 1.66258e-05 | 0.00288316 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152808 | GGAGAATTCAATGGC[A/G]TTGACACAGCCGAAG | 8816 |
rs760008271 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107942 | GCACCTGCCCTTAAA[A/C]ATTCATAGAAAAACA | 8816 |
rs760029384 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155112 | CCAGTTTCCCTGCTC[A/G]CTGTTCCTTTGCTTG | 8816 |
rs760066083 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065231 | CCTCCTGAGTAGCTG[A/G]GATTACAGGCATCCA | 8816 |
rs760081032 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096434 | CTTTTTGAATCTCCA[C/T]AAATTTAAGTTTGAC | 8816 |
rs760086422 | snp | G/T | 1.66247e-05 | 0.00288307 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122397 | TGTGCTTAAAACAGC[G/T]GACATCGCAAGGCTG | 8816 |
rs760090162 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113525 | TCCTTAAAATCTCTC[C/T]CTACACTTGAAGTAT | 8816 |
rs760115268 | in-del | -/CGCGCCGCCGCC | 0.000103686 | 0.00719946 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153002 | GCCGCCGCCGCCGCT[-/CGCGCCGCCGCC]CGCGCCGCCGCCCCT | 8816 |
rs760171457 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084302 | ATCACTGTGGTCACA[A/C]CAGGCTGTCTGCTGG | 8816 |
rs760175792 | snp | C/T | 7.11086e-05 | 0.00596232 | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091088 | GTCAACATCAGCATC[C/T]CCATTCCTGGTGAGA | 8816 |
rs760260913 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117697 | ACTCACACGACAATC[C/T]CCTTTAAACAGAGTT | 8816 |
rs760265175 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069201 | GCCCAAAAAAATGCA[C/T]TTACAGCTGTTTCCA | 8816 |
rs760265812 | snp | A/C | 2.08548e-05 | 0.00322908 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152977 | CCAGCTCTCCTCTTC[A/C]TGCTGGAACCGCCGC | 8816 |
rs760298625 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095778 | ATTACTATAAATCCA[C/T]GATTAACTAATCCAT | 8816 |
rs760323886 | snp | A/G | 4.9588e-05 | 0.00497911 | missense | DCAF5 | GRCh38.p7 | 14:69055233 | TGGTGACCCGCAGGG[A/G]CCCCAGGTGGAAGGC | 8816 |
rs760401575 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071555 | GCCTGCCTTAGAATC[A/G]TATATCCAAAAGGTA | 8816 |
rs760453613 | in-del | -/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118948 | TTCTCTTCTAAACTC[-/TT]GTTTTAAATTTTCAC | 8816 |
rs760454658 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137109 | TTAAATTATGAATGG[C/G]TGGGAGGCCTATCTT | 8816 |
rs760471537 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125420 | TTAATGTCTAGAAGA[-/T]GCAAAGAATTTCTAC | 8816 |
rs760503316 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123448 | TATCTAGATGGCTAT[A/G]AAAGAAGCTGTTTAT | 8816 |
rs760569588 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060437 | GAAATGTGTGCTGCA[A/G]TGAAAGTCAGCTCTG | 8816 |
rs760572996 | snp | A/G | 3.29951e-05 | 0.00406159 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118221 | GTTGTCATTCACTGG[A/G]CTCACAGACAAGCCA | 8816 |
rs760615501 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062283 | ATTCTGATAGACCTT[C/T]AGTATGTTTAAATAT | 8816 |
rs760659369 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064100 | CCTAGCACTGGCTTC[C/T]TAAGGTGGTATGAAA | 8816 |
rs760660971 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116458 | GTTAAACATGACACT[A/G]TGAAAGGCTGATGGA | 8816 |
rs760709856 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076143 | AAATTGACAAGTATT[A/G]GCAAGGATGTGGAGA | 8816 |
rs760715310 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69075376 | AGGAATTCTCCACAT[A/G]TACAGGTTGAAGTCA | 8816 |
rs760717874 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113472 | CTCAGATACACAAGC[C/T]ATACAATTTTACCTG | 8816 |
rs760821511 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100822 | ATTATTATTGAGAGT[A/G]TACTAAGAAGTCCCT | 8816 |
rs760824503 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079047 | TACACGTTTAAAAGA[A/G]GCTATCAACTTCATG | 8816 |
rs760841876 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112597 | GATATATATGTATAC[-/AC]ACACACACACACACA | 8816 |
rs760848732 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093799 | GATTGGAATGAAAGT[-/AA]AGAGGGAAGACTTAG | 8816 |
rs760886238 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085279 | GGCAAGCAGAAAAAG[C/T]GAGTAGGCAGTGGTG | 8816 |
rs760949809 | snp | A/G | 0.000181346 | 0.00952051 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062489 | CACCATGAAGGCTCC[A/G]TTGACCACCCTACCA | 8816 |
rs760979742 | snp | A/T | 1.64977e-05 | 0.00287203 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122195 | CACAGTGACGTTCCC[A/T]AGGTAGAATCTCCCT | 8816 |
rs760985782 | snp | A/G | 0.000117307 | 0.00765766 | missense | DCAF5 | GRCh38.p7 | 14:69053885 | TTCTTCTCTGAGGAG[A/G]AATTCTCTGAATCTG | 8816 |
rs761046744 | snp | A/T | 1.65523e-05 | 0.00287678 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122364 | GGTCATCTCCTCCTT[A/T]AGAAGGAAATAAGAA | 8816 |
rs761058871 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139053 | CTACTCCAGAGGTTG[A/G]GGTGGGAGGATCACT | 8816 |
rs761069815 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054945 | CATTCCGCTGCCAGG[C/T]AGAGGCTCGGCGTTC | 8816 |
rs761078114 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153891 | TAAAGAAGTAGGAAG[A/G]AAATTGCCAAAACCG | 8816 |
rs761079601 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105548 | CAGGGAGAACATGAC[C/T]CGCCTTTAATGTGGG | 8816 |
rs761118361 | in-del | -/CAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148102 | TGTTCATTTTCTTCG[-/CAA]AAAAAAAAAAAAAAA | 8816 |
rs761132724 | in-del | -/GTC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144452 | TGGCGGGTGCCTGTA[-/GTC]CCAACTACTCGGGAG | 8816 |
rs761188357 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143709 | GCTTATATTATAATG[A/G]CAGTGGCGACTAATA | 8816 |
rs761197005 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091242 | AAGAAAAAGATGGCA[A/T]CCCAAGAGGCCATTC | 8816 |
rs761197096 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077987 | GGTGGCTCTGTAAGG[C/T]TCATTTAATTCTAAG | 8816 |
rs761219550 | in-del | -/ACACACACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099252 | TGGGACTCTGTCTCA[-/ACACACACAC]ACACACACACACACA | 8816 |
rs761223931 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057129 | TTTTAACCACTCAAG[C/G]GATGAGTAAGTAGGG | 8816 |
rs761223962 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112702 | TAGAAGCTACCTCAT[A/T]GGGTTATCATAAGGA | 8816 |
rs761276992 | snp | C/G | 1.64792e-05 | 0.00287042 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054115 | TGGGGAAGAGTAGGC[C/G]ACCACCTCCAGCTCC | 8816 |
rs761291541 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094079 | ATCAGTATGGAGTGT[A/G]CAAATAAACCAGCAT | 8816 |
rs761368086 | in-del | -/G | 1.65153e-05 | 0.00287356 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062365 | TTCTCTAAAAGGACA[-/G]AAGGGGAAGGTGCCT | 8816 |
rs761368253 | snp | C/T | 4.94548e-05 | 0.00497242 | missense | DCAF5 | GRCh38.p7 | 14:69055133 | CGTTTGTCTTGGTAG[C/T]GCCGCAGAGCAGACA | 8816 |
rs761376353 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130000 | ATAATCACATTGTGG[C/T]AGCAGCTTTGTAGTT | 8816 |
rs761382829 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119091 | AGCTGGTTTCATGTT[-/G]TTTTTTTCAAAAAAC | 8816 |
rs761386187 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058383 | AATTAGCTGGGCGTG[A/G]TGACAGGTGCCTGTA | 8816 |
rs761395258 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147321 | TTGAAGGTATCAATC[-/T]CCTGAAAGCCTTTTG | 8816 |
rs761395840 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082450 | ACCTTTATGGGTTCT[A/G]TGTAGAAAAAATTCT | 8816 |
rs761405897 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060311 | GGCAGGGCTCTATCC[C/T]AGCTTTGCCACCAAT | 8816 |
rs761453392 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108910 | CACCTGACTCTTCTC[G/T]TTCTCTCTTTTGTCC | 8816 |
rs761474613 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121503 | GCAATTTCTTAAAGT[C/T]AAACCTAATAGCTTA | 8816 |
rs761483323 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080980 | GAGGGGGAAACCACA[A/G]ATTAAAAACTCACTT | 8816 |
rs761500905 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086399 | AAAAAAACATAATAG[C/T]GGATATGAAAATGCT | 8816 |
rs761521600 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052205 | TCCTTTTGGCTTAAA[C/T]CAACCACCTTGTGTT | 8816 |
rs761529363 | in-del | -/TTTC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104335 | ACTAGGCATTTTTAA[-/TTTC]TTTATGGATACACAC | 8816 |
rs761552015 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148769 | CATATAACATTTCAT[A/T]GACCATTCACTACCC | 8816 |
rs761662849 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136241 | CTACCTCAGCCTCCA[C/G]AGTAGTTGAGACTAC | 8816 |
rs761695192 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073239 | GAACATCTAGAAGGT[A/G]ACATGAGAACTTCCT | 8816 |
rs761700687 | snp | A/G | 2.69291e-05 | 0.00366931 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091904 | TGGAAGGCACAAGGC[A/G]CAGGAATCAGGCATG | 8816 |
rs761711883 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076723 | GCTGCACAGCAATGT[A/G]ATTGTACTTAATGCC | 8816 |
rs761736212 | snp | C/T | 1.65203e-05 | 0.002874 | missense | DCAF5 | GRCh38.p7 | 14:69054383 | TGCTCTACAGAGCCG[C/T]TATTGCCAGTGTCCT | 8816 |
rs761783064 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076471 | TTTAAAAGGAATGAA[A/G]TTCTGACACATGCTA | 8816 |
rs761796871 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | DCAF5 | GRCh38.p7 | 14:69054497 | TCTTTAAAAGTGTCC[C/T]TGCTGCAGCCTTCAG | 8816 |
rs761818691 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062473 | ATCGATGCCCTTTCA[A/G]CACCATGAAGGCTCC | 8816 |
rs761819979 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095429 | AACAGGGTAGGAGGT[A/G]ATCCAAGGTGATCCA | 8816 |
rs761856932 | snp | C/T | 0.000148553 | 0.0086171 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122188 | TCCCAACCACAGTGA[C/T]GTTCCCAAGGTAGAA | 8816 |
rs761904473 | snp | A/G | 1.72531e-05 | 0.00293705 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055632 | CAGAAAATGAAAAAC[A/G]AAAGCAACAAGGAGT | 8816 |
rs761906625 | snp | C/T | 1.65192e-05 | 0.00287391 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122335 | TTGTTCCATGTGCCA[C/T]AGCAGAACCCGGCGG | 8816 |
rs761917965 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080948 | GTTATTTTTTTTAAC[A/G]TCATTCTAAACATGA | 8816 |
rs761921026 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138910 | CAGCACTCTGGGAAG[C/T]TGAGGTGGGTGGATT | 8816 |
rs762080413 | snp | A/G | 1.65173e-05 | 0.00287374 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69119205 | TTACCTTTCAACATC[A/G]TGGAGGATAACTTGC | 8816 |
rs762111007 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112232 | TATGCAGATTTCCAG[G/T]GTTATAAAAGGTAAG | 8816 |
rs762133755 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077797 | CTAAATACTGTGCAA[C/T]CATTTAAAATCAATT | 8816 |
rs762163239 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088496 | TTTTATTTTGAGGCT[A/C]ATGAATTACCTAGTG | 8816 |
rs762183884 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69055762 | AAAATAAGTTCTTTA[C/G]CAGACTGGATCATGT | 8816 |
rs762217578 | in-del | -/TATA | 6.46893e-05 | 0.00568687 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091047 | TGCAAGAAGGCCAAG[-/TATA]TATATTCTTAAACTG | 8816 |
rs762226501 | snp | A/G | 5.03309e-05 | 0.00501627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091657 | AGTGTGAGATGCAGG[A/G]GGCAGACAGCATTTA | 8816 |
rs762239450 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102810 | ACTTTTTTTAATAAG[C/T]AGGAATATACACTAA | 8816 |
rs762280361 | in-del | -/AAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072625 | GAGACCCTGACTTTA[-/AAA]AAAAAAAAAAAAAAA | 8816 |
rs762295501 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137832 | ACATAACTTTTATTA[C/T]AGTATAATATTATAA | 8816 |
rs762297198 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131417 | CTGCAGCGCATTACA[C/G]AGGCACAGTCTGTGT | 8816 |
rs762408048 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | DCAF5 | GRCh38.p7 | 14:69055101 | CAGAATCGGACTCAT[C/T]GGAAAGGGCCAGGAG | 8816 |
rs762416134 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108004 | CCTTTCTGTGAAGCA[A/G]CTCCTGGGCACTGGG | 8816 |
rs762437442 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104464 | GTCAGAGGAATATGC[C/T]AAATTACAGTAGAAG | 8816 |
rs762481039 | snp | C/T | 1.65759e-05 | 0.00287883 | missense | DCAF5 | GRCh38.p7 | 14:69053912 | TCTGTATCTTCCAAT[C/T]CAATTCGTTGCCTTT | 8816 |
rs762498026 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054955 | CCAGGTAGAGGCTCG[C/G]CGTTCATTCAGCTCC | 8816 |
rs762498044 | snp | C/G | 1.65108e-05 | 0.00287317 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116368 | AAAGGGGGCTCACCT[C/G]TGAGGTTTTCGAATG | 8816 |
rs762501112 | in-del | -/G | 1.64942e-05 | 0.00287173 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075309 | AGGTCAACAGAGCCA[-/G]CAATAGCAGTACATT | 8816 |
rs762515964 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057610 | ATGAAAGTCATAACA[A/C]TGAAAGTTAGTTTGC | 8816 |
rs762530494 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093787 | TAATCCTTTTAGGAT[C/T]GGAATGAAAGTAAAG | 8816 |
rs762546126 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073108 | CTGCTAGATGTATTC[A/C]GTTAATCCATAAATG | 8816 |
rs762548714 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111999 | CCCTTAACTAACATC[-/A]TAAAGGTTTTGGCTG | 8816 |
rs762561818 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058665 | GGATCGCTTGAGCCC[A/G]GGAATTTGAGACCAA | 8816 |
rs762581037 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121368 | TAGACCTGACAGGAC[C/T]TGGTGACAGACTAGA | 8816 |
rs762588657 | snp | A/G | 4.26412e-05 | 0.00461723 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091877 | GGTTTCCACCATAGC[A/G]CAGGAGAGAACTGGA | 8816 |
rs762645128 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081590 | AGATACTAACTTGCT[C/T]GAGCATAGGAAGAGA | 8816 |
rs762796858 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148015 | CAACATATAAAAAGG[C/T]GGAGTAACAATCCAA | 8816 |
rs762843494 | snp | A/G | 1.65244e-05 | 0.00287436 | missense | DCAF5 | GRCh38.p7 | 14:69054365 | TTCTTGGTTTCAAAA[A/G]GGTGCTCTACAGAGC | 8816 |
rs762876000 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096915 | GTTCAATGAATAGTC[A/G]TTGGCAAGAAGGAAA | 8816 |
rs762923915 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071373 | AAGAAAAAGAAGGCC[C/T]TGACTTTGGCTCACA | 8816 |
rs762928342 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086265 | CCGGAGGCTGTGGCA[C/T]GAGAATTGCTTGAAC | 8816 |
rs762933242 | snp | A/G | 9.90655e-05 | 0.00703725 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055570 | CTCAATCCGACCGTC[A/G]AGGTCTCCAGTACAT | 8816 |
rs762964380 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119167 | AAAACAAAGTCAATC[A/G]CCTTCACACACCACC | 8816 |
rs762968878 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | DCAF5 | GRCh38.p7 | 14:69054243 | TGTCATCAGACTGGG[C/T]CCTGGGACAGTTGCC | 8816 |
rs762983636 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137597 | TAACACTTCTAGGAA[C/T]GCACACTACACCCAG | 8816 |
rs763007726 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102399 | GGCATGAGCCACCGC[A/G]CCCGACCATTAGTTT | 8816 |
rs763019457 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085133 | GGAAGCATATAAATC[A/T]TACATACAAACCTAC | 8816 |
rs763068383 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104210 | ATTACATATTCCCAC[A/C]AGCAATATGTGAGTG | 8816 |
rs763073737 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150126 | AAGGAACAAATAGGA[A/G]AAGCTAGGTGTATCT | 8816 |
rs763099002 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076282 | GATGCAGCAATTACA[A/G]TCCTAGGTATATATC | 8816 |
rs763237918 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123601 | ATTTGTGCTGTTGTA[C/T]AGCCACTGCCATTAT | 8816 |
rs763257853 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054824 | GAGAGGTCATCCACT[C/T]TGATCTGGGGGTAAT | 8816 |
rs763270688 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088290 | GCCTACAAACTTGTA[C/T]GTGTTGTGACTTGTG | 8816 |
rs763337659 | snp | A/G | 1.8014e-05 | 0.00300111 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152961 | CATGCTGCCCCCCAG[A/G]CCAGCTCTCCTCTTC | 8816 |
rs763338173 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120226 | GTAGCTGGAACTACA[A/G]GCATGTGTCACTATG | 8816 |
rs763368894 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115051 | GCAGTTTGTCCAAAT[C/T]CTGCCTTTTGTAATA | 8816 |
rs763434688 | snp | G/T | 4.4288e-05 | 0.00470553 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091069 | CTTAAACTGCCAGCT[G/T]TAAGTCAACATCAGC | 8816 |
rs763504037 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052567 | CCGAGTGACTGCAAC[A/G]CTGAAAATCTGTTGC | 8816 |
rs763540463 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69092085 | CTTCAATTGTCAGTT[A/C]TCTTGCTCAGTCTCC | 8816 |
rs763548863 | snp | A/T | 1.67044e-05 | 0.00288997 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075426 | ACTGTTGGAACAAAA[A/T]ATATATAGATAACAT | 8816 |
rs763567242 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116193 | GAGTACGGATTTGTC[A/G]CTGTCTATTCCTTGG | 8816 |
rs763596947 | snp | C/T | 1.65641e-05 | 0.00287781 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69053917 | ATCTTCCAATTCAAT[C/T]CGTTGCCTTTTGAGG | 8816 |
rs763627724 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108011 | GTGAAGCAGCTCCTG[C/G]GCACTGGGAAGGAAA | 8816 |
rs763665148 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058680 | AGGAATTTGAGACCA[A/G]TCTGGACAACATGGC | 8816 |
rs763734117 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093788 | AATCCTTTTAGGATT[A/G]GAATGAAAGTAAAGA | 8816 |
rs763740657 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133963 | TAGGGTTTTGAAATA[C/G]TAACCCTAGACAATG | 8816 |
rs763750777 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057686 | TGAAGCCTGGAGTAA[C/T]GGAGTGAAACACAGG | 8816 |
rs763752910 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073188 | TAACTATTTTTTAAG[C/G]AACTACTAAATAAAC | 8816 |
rs763772712 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054878 | GTGTTGGTGGGCTTG[A/C]TTGGGGCACTGGGCT | 8816 |
rs763782061 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091716 | GCTTTTCATGGTGCA[C/T]GAGTTGAAGTAACCC | 8816 |
rs763794619 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079730 | GGCAGAGTTGATCAA[A/G]AGAGACCCTGTTCCT | 8816 |
rs763851357 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104201 | GGCTATACCATTACA[C/T]ATTCCCACCAGCAAT | 8816 |
rs763891031 | snp | A/G | 6.60971e-05 | 0.00574841 | missense | DCAF5 | GRCh38.p7 | 14:69054366 | TCTTGGTTTCAAAAG[A/G]GTGCTCTACAGAGCC | 8816 |
rs763903967 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085171 | ATTCTCTGAAACAGA[G/T]CTTTAATGTTTAATA | 8816 |
rs763961602 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133030 | GCTAGATAAATGTCA[C/G]CTAATTATTATGCTA | 8816 |
rs763993683 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106460 | TGCAGCCTCAACCTC[A/C]TGGGCTCAAGCGATC | 8816 |
rs763993984 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099485 | GAGATCTGTGGTCCA[C/T]AGTGATTTATCAATG | 8816 |
rs764018258 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154857 | ATCATTTATTTTTGT[A/G]ATGATATGAGTCTCC | 8816 |
rs764042346 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087851 | TGTCTCCATGAGTTA[C/G]TGACAGACCATGGCA | 8816 |
rs764129326 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071429 | TCTCAGCACTCGGCA[C/T]GCACATGAAACACAC | 8816 |
rs764156445 | snp | A/G | 4.94597e-05 | 0.00497266 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054247 | ATCAGACTGGGTCCT[A/G]GGACAGTTGCCAGAC | 8816 |
rs764156740 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120262 | CTAATTAAAAAAAAA[A/T]TTTTTTTTGTAGAGA | 8816 |
rs764197261 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126748 | AGGGGCCAAAAACAG[A/G]CCCACGTAAGTATAA | 8816 |
rs764246328 | snp | C/T | 1.64901e-05 | 0.00287137 | missense | DCAF5 | GRCh38.p7 | 14:69055380 | TCTCACTGAGGTCAC[C/T]GTCTGAGTCAGAGCT | 8816 |
rs764288029 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123702 | CCTAGTCACTGTTCT[A/T]TTTTTTTGAGACGGA | 8816 |
rs764294233 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101390 | TGTCACACACATGGA[G/T]TCAAAGATGTTACCG | 8816 |
rs764322497 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066090 | AAACCAACAGTCATT[C/T]CTCTGGGCCATCTGC | 8816 |
rs764410368 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144746 | TCCAGAAACTGCTAA[A/C]ATTCAGCTTTCAATT | 8816 |
rs764412464 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080796 | TGACTTCACAACCAA[C/T]GTTCATATTTAATAC | 8816 |
rs764478804 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060018 | AGATTTATCACAGAA[A/G]CATCCCAGAGTGCAC | 8816 |
rs764485012 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116320 | CACATTACCTGAGAA[A/T]TGAGGCAGAGGAAAG | 8816 |
rs764517601 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051134 | AATCATTAACAAAAC[C/G]AGCTGGAAAATAGAG | 8816 |
rs764537617 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150160 | CCAAAATGGAGGAGC[A/G]ATGGAATAGCCTGCT | 8816 |
rs764541966 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136903 | AGTTTTAAAATATTA[A/T]TCTTAATATTACAAA | 8816 |
rs764565635 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065282 | TTGTATTTTCAGTAG[A/C]GACGGGGTTTCACCA | 8816 |
rs764569221 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | DCAF5 | GRCh38.p7 | 14:69054750 | AAGTTGGTGATGCCC[A/G]GCTTGGTTGAATCTC | 8816 |
rs764572364 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112737 | ATGAGGTAATTATTC[A/C]TATGATGGTCAATAC | 8816 |
rs764574980 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115115 | TGAAGTAGCAGAGAA[C/T]ACTGCAGATGAACAC | 8816 |
rs764615084 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056313 | GTTAGCTATAGGAGT[A/G]GGTAGGACACATGCC | 8816 |
rs764646959 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102682 | TTCTACCTTCACATC[C/T]GTTCTACTAACATCT | 8816 |
rs764651372 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148037 | ACAATCCAAGTCAAA[C/T]GCACATAGAGATACA | 8816 |
rs764658821 | snp | C/T | 3.93306e-05 | 0.00443438 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091078 | CCAGCTTTAAGTCAA[C/T]ATCAGCATCTCCATT | 8816 |
rs764666058 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054859 | GTTGTCTTCTCCAAT[A/G]TAAGTGTTGGTGGGC | 8816 |
rs764710189 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052601 | TTTCTCTTCTAAACC[G/T]GTATCTACCTCAATA | 8816 |
rs764745739 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120072 | GGATCTTGCTCTGTT[C/T]GTCTTTTAAAAATTT | 8816 |
rs764748717 | snp | C/T | 3.36242e-05 | 0.00410012 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075430 | TTGGAACAAAAAATA[C/T]ATAGATAACATTATA | 8816 |
rs764841902 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104714 | TACCAAAAATTAGCC[A/G]AGTGTAGCAGCGGGC | 8816 |
rs764852627 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107984 | ACATATTAGGACAAA[G/T]GCCTCCTTTCTGTGA | 8816 |
rs764922026 | snp | A/G | 3.53076e-05 | 0.0042015 | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091118 | ACTCAGAAAAGGCTG[A/G]AAACTCACAGCTTGG | 8816 |
rs764927473 | snp | A/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090073 | AATAAAGCCTAGTAA[A/T]CTATTAATATCACCT | 8816 |
rs764938861 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140604 | TCAAAATCAACTCTA[C/G]AAAGAACAACAACCC | 8816 |
rs764954044 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057460 | GAAGATAAATCTATT[C/T]GTACCTCACAGAAAC | 8816 |
rs765063787 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096699 | CAAATTAAGAGGCAG[C/T]ATAATAACAGATTTA | 8816 |
rs765071737 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077622 | GGCTCAAGGGATCCT[C/T]CTGCCTCAGCCTCCC | 8816 |
rs765124057 | snp | A/G | 1.65318e-05 | 0.002875 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119151 | GCCTCTTCATATATG[A/G]AAAACAAAGTCAATC | 8816 |
rs765124909 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | DCAF5 | GRCh38.p7 | 14:69054221 | GTTTCGAGGCTCCTC[C/T]CCTCACTGTCATCAG | 8816 |
rs765151432 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095997 | GGAGAAAGTCTCTCC[C/G]CATCACAGTTTCTGA | 8816 |
rs765158451 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146455 | TATCCTTATGACATG[A/T]TCTTTATAATTTATC | 8816 |
rs765257790 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083815 | AGTGCCAAGTCTCCT[A/G]AAGAAACAGAAAATA | 8816 |
rs765258125 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095590 | CAATTGGACTTCTTT[A/T]TTGCTCTGGTGGGGT | 8816 |
rs765273598 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132162 | GGTATATAACCAGAA[C/G]TGAAATTGCTGGATC | 8816 |
rs765301415 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148944 | ACATTGTGCCTCCAC[A/G]TTCCACATCAAAAAG | 8816 |
rs765302684 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055246 | GGGCCCCAGGTGGAA[A/G]GCGTTGTCGGCAGAC | 8816 |
rs765343291 | snp | A/C | 0.0111258 | 0.0737504 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118230 | CACTGGGCTCACAGA[A/C]AAGCCATATACTGCA | 8816 |
rs765375784 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134862 | TTAACCATCTTGGAG[A/G]ACAATTGGGTGACAT | 8816 |
rs765378550 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052430 | TGCACTCAAGAAAGT[C/T]ATATTGTTTTTCTCT | 8816 |
rs765390016 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101175 | TGCTTCTTGGTTCAA[C/G]AAGATTTCACAGAAT | 8816 |
rs765438318 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087350 | ACAAAACAAAAATCC[A/C]AGTAGGAAGTGAAAG | 8816 |
rs765442285 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073523 | CTGGGCACAGTGGCT[C/T]ATGCCTATACGCCCA | 8816 |
rs765468355 | in-del | -/TTTTTTTTTAGACGGAGTTTCACTTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126161 | CAGAGATTCTTTTTT[lengthTooLong]TTTTTTTTTAGACGG | 8816 |
rs765472533 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079213 | TTCGGCTATTCATCA[A/G]GGCAAAGCCATGAGA | 8816 |
rs765473186 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065986 | GTCCTGACTGAATCG[C/T]TAATAATGGGTACCC | 8816 |
rs765560186 | in-del | -/ATG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115483 | CATCACTTAGTTTCC[-/ATG]ATATTCTTCTGCAAC | 8816 |
rs765577000 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148326 | CAATGTTGTTCCCCA[A/T]CCCTCAAAGGACTAA | 8816 |
rs765676785 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078124 | AGACAAGGAAACTCA[A/T]AAGGCCAGTCTTGTT | 8816 |
rs765706902 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127160 | AAAGGAGTTGAAACT[C/T]GTATCTACACAAAGA | 8816 |
rs765777045 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084818 | TCAGGAACACTATTG[G/T]GTACAGATGTGGCAG | 8816 |
rs765788180 | snp | A/G | 1.65414e-05 | 0.00287583 | missense | DCAF5 | GRCh38.p7 | 14:69054018 | CATTGGGGGTCTCAC[A/G]GGCCATTTCAGACCC | 8816 |
rs765797848 | snp | A/G | 0.000174322 | 0.00933439 | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091091 | AACATCAGCATCTCC[A/G]TTCCTGGTGAGACTC | 8816 |
rs765826984 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067879 | TGACCTCGTGATCTG[A/C]CCACCTTGGCCTCCC | 8816 |
rs765832663 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116665 | CTACTTACAAGGTCC[C/G]CATGAGTCCTATACA | 8816 |
rs765848092 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065237 | GAGTAGCTGGGATTA[A/C]AGGCATCCACCACCA | 8816 |
rs765850803 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117759 | GGTAATTTGAGATTC[A/G]GTGGTTCTTTCAACA | 8816 |
rs765899313 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131909 | TGCCATTCTCCCCCT[A/G]GACACCATTCACTTG | 8816 |
rs765908952 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128466 | GCTGGGATTACAGGC[A/G]TGAGCCTGGCTGAAT | 8816 |
rs765952186 | snp | A/T | 2.15971e-05 | 0.00328604 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152978 | CAGCTCTCCTCTTCA[A/T]GCTGGAACCGCCGCC | 8816 |
rs766016283 | in-del | -/A | 1.66427e-05 | 0.00288462 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075421 | ATATACTGTTGGAAC[-/A]AAAAAATATATAGAT | 8816 |
rs766043736 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104710 | AAAATACCAAAAATT[A/T]GCCGAGTGTAGCAGC | 8816 |
rs766060319 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069373 | ATGCAAGAACAACTC[A/T]ATCAGCCATTCCAGG | 8816 |
rs766079527 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152265 | CCGGGTCGCAGCCCC[C/T]GGCCCCTCGGCGTCC | 8816 |
rs766102697 | snp | C/T | 6.61452e-05 | 0.0057505 | missense | DCAF5 | GRCh38.p7 | 14:69054033 | AGGCCATTTCAGACC[C/T]GCAACAATCTTTGTG | 8816 |
rs766119423 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061758 | AGGTTTGGAAAACAG[-/A]AATACATTATACTCA | 8816 |
rs766123627 | snp | A/T | 1.648e-05 | 0.0028705 | missense | DCAF5 | GRCh38.p7 | 14:69054149 | AAGTTCTGCCCGTTA[A/T]TGTGAGGGTGAGGGG | 8816 |
rs766129782 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094495 | CTAGAATGCTTAGGG[A/G]TGCTATTTAAAGAGC | 8816 |
rs766174580 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150944 | GCAACGTGTGACTAC[C/T]TACAATTCCGTTAAC | 8816 |
rs766214361 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074875 | CCTGTTTCTACTAAA[A/G]ATACAAAAAATTAGC | 8816 |
rs766215683 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123472 | TGTTTATAGTGCCAA[C/T]TATAACTGGTAGGCT | 8816 |
rs766234559 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130268 | GTTTGAAGAGCCAAA[A/G]AAGAATAATTTAAAT | 8816 |
rs766275804 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130298 | TGTCCATCAACAGAA[C/G]TCTGGTTAAAATTAT | 8816 |
rs766293122 | snp | A/G | 1.65474e-05 | 0.00287636 | missense | DCAF5 | GRCh38.p7 | 14:69055238 | ACCCGCAGGGGCCCC[A/G]GGTGGAAGGCGTTGT | 8816 |
rs766297205 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109490 | CATGCCTTCCTTAGT[C/G]AATACCTTACCCAGA | 8816 |
rs766329432 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065074 | AAAACTGTTTCTCTT[A/G]CACTTTCATGCAATA | 8816 |
rs766367860 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143792 | TTTTCTATAAAGTAA[C/T]GGATCATGGTTATAA | 8816 |
rs766382896 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118223 | TGTCATTCACTGGGC[C/T]CACAGACAAGCCATA | 8816 |
rs766382951 | snp | C/G | 1.64887e-05 | 0.00287125 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055138 | GTCTTGGTAGCGCCG[C/G]AGAGCAGACAGACGC | 8816 |
rs766419346 | in-del | -/TTAT/TTATTTAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077373 | ATGTAGCTTATTTAT[-/TTAT/TTATTTAT]TTATTTATTTATTTA | 8816 |
rs766451307 | snp | C/T | 1.65083e-05 | 0.00287296 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054619 | TGCTCTCCCTTCATC[C/T]GCCTCCCCGGTCACC | 8816 |
rs766476000 | snp | G/T | 1.64874e-05 | 0.00287113 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116478 | AGGCTGATGGATAGT[G/T]TGCCAGGCAGAAGGG | 8816 |
rs766480480 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113494 | TTTTACCTGCAGTTA[C/T]AGGGGATTCACAAAT | 8816 |
rs766493780 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146737 | CTGTTTTACAAACAG[C/T]ATGCACTCAAAAACT | 8816 |
rs766537753 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | DCAF5 | GRCh38.p7 | 14:69054518 | CAGCCTTCAGGTGGC[A/G]GGTCCTGGTTCCTCT | 8816 |
rs766546673 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062492 | CATGAAGGCTCCGTT[A/G]ACCACCCTACCAATG | 8816 |
rs766575220 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148242 | TAAACCCAAGATATC[C/G]CCTAAATATGCGTAC | 8816 |
rs766584931 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100883 | ACATAAGGTCAAACC[C/T]GGAATTACAAAATAG | 8816 |
rs766614815 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148449 | CACCTGTAATCCCAG[A/G]ACTTTGGGAGGCTGA | 8816 |
rs766636267 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122376 | CTTAAGAAGGAAATA[A/G]GAATCTGTGCTTAAA | 8816 |
rs766654912 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139339 | AAAATTAAAAATTAG[C/T]TGGACGTGGTGATGC | 8816 |
rs766683414 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105572 | ATGTGGGCAGGCATT[G/T]TTCCAGTGTAACTAG | 8816 |
rs766755378 | snp | G/T | 5.34697e-05 | 0.0051703 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055652 | CAACAAGGAGTAACT[G/T]GAAAGTATTCTTTCA | 8816 |
rs766766313 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133066 | ACTCAAACAACAGCT[A/T]ACATCAGTTAAGTTT | 8816 |
rs766777528 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053249 | CTCAATAAAGAAGTG[C/T]TACTTAGAGAAAACA | 8816 |
rs766790890 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089932 | AAGGATGGGAAACCA[C/T]GGTCTAGGTGCTTAC | 8816 |
rs766791445 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056116 | TAATATCTGAGCCTA[C/T]AGCTCCACTTCTGCC | 8816 |
rs766800879 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076647 | GAATGAAGAGTTAGC[A/G]TTTGTTGGGGAGTTT | 8816 |
rs766807202 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123430 | CTTGTATTTGCATAG[A/C]CCTATCTAGATGGCT | 8816 |
rs766845624 | snp | A/G | 1.64969e-05 | 0.00287196 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122197 | CAGTGACGTTCCCAA[A/G]GTAGAATCTCCCTTT | 8816 |
rs766852801 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112701 | ATAGAAGCTACCTCA[C/T]AGGGTTATCATAAGG | 8816 |
rs766866299 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125558 | ATCAGGGAAATGTAC[A/G]TTATAATTTAGACAG | 8816 |
rs766884190 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087198 | AAGTGCTGTCTTATA[C/T]GTGCATGCCAGAAAA | 8816 |
rs766927334 | in-del | -/TTGTTA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137869 | ACTTTATTACTATTG[-/TTGTTA]TTGTTAATGTATTAC | 8816 |
rs766931980 | snp | C/T | 3.32662e-05 | 0.00407824 | missense, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152861 | AGAGGTTTCTGCAGC[C/T]CCGCAGGCGTCTCCT | 8816 |
rs766963181 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081013 | TGTTCTGCTTTAGTA[C/G]TAAAAAAAGGCAATA | 8816 |
rs766964255 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140420 | ATAGCTATCCCAAAA[A/T]ATTAAGCCTATAACA | 8816 |
rs766965212 | in-del | -/TG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081752 | GACCTTTATAGAAAA[-/TG]TGTGTGTGTGTGTGT | 8816 |
rs766972333 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | DCAF5 | GRCh38.p7 | 14:69054948 | TCCGCTGCCAGGTAG[A/C]GGCTCGGCGTTCATT | 8816 |
rs766978682 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094111 | TGTAGGACTGACTAG[C/G]AGTTGGGGGTTGGAA | 8816 |
rs767020168 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | DCAF5 | GRCh38.p7 | 14:69054122 | GAGTAGGCCACCACC[C/T]CCAGCTCCCCCAAGT | 8816 |
rs767112073 | snp | C/T | 1.65381e-05 | 0.00287555 | missense | DCAF5 | GRCh38.p7 | 14:69054024 | GGGTCTCACAGGCCA[C/T]TTCAGACCCGCAACA | 8816 |
rs767129806 | snp | A/G | 7.59388e-05 | 0.00616146 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152724 | AGGGGGAGGCTGGGA[A/G]GGTGCGGGGAGGCGC | 8816 |
rs767161221 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082570 | TAACAAAGTGGCCAG[C/T]GTTACTTAAAGATGA | 8816 |
rs767161321 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066415 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCT | 8816 |
rs767203945 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | DCAF5 | GRCh38.p7 | 14:69054979 | CAGCTCCTCCTCATC[C/G]TCAGAGCTGCTAGAG | 8816 |
rs767240058 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055135 | TTTGTCTTGGTAGCG[C/T]CGCAGAGCAGACAGA | 8816 |
rs767266756 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051626 | CCAAATGAGATTAAG[G/T]CTTTTAACATGAAAA | 8816 |
rs767276007 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130398 | ATCAGAGACAAAGTA[-/G]GAATGGCAGTGGCCA | 8816 |
rs767291617 | snp | A/C | 6.44039e-05 | 0.00567431 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091917 | GCACAGGAATCAGGC[A/C]TGAGATAGGCTAAAC | 8816 |
rs767295080 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073440 | ACCCAGTCTGTGATA[C/T]TTCGTTATTGCAGCT | 8816 |
rs767334656 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102856 | TACAATACAGTAAAC[A/G]GGTAAACCAGTAACA | 8816 |
rs767379442 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152047 | CCTACCGCCTGCCTC[A/G]CAAGTTGCGCATTCA | 8816 |
rs767394052 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142749 | GGTATTTTCTCCCCA[C/T]GTATAACTATATGAG | 8816 |
rs767422389 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071017 | AGCCAGATTGGTCTC[-/A]AAACTCCTGACTTCA | 8816 |
rs767443788 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121504 | CAATTTCTTAAAGTT[A/G]AACCTAATAGCTTAT | 8816 |
rs767455072 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077842 | ACACTTGTAGGAACA[C/T]GAGAAAAAAGGCAAA | 8816 |
rs767479282 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69092612 | GAGAGAACAAGACTC[C/T]ATCTCAAAAAATTGA | 8816 |
rs767520842 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112279 | TAGGCCATGAGACAG[C/T]GAAAAAGGGTTTAAC | 8816 |
rs767521200 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112546 | CTAAAAATAAAAACT[-/T]AAAAAAAAGAAAAAA | 8816 |
rs767536923 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121018 | TTAGGGGAATTGGTG[A/G]GGACTGGACAATTAA | 8816 |
rs767598270 | in-del | -/AGA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073770 | AGAATAGTCCTGGGG[-/AGA]AGAAGGATTATCCAC | 8816 |
rs767622786 | snp | C/G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096997 | ACAGTGCAGAAGGAG[C/G/T]GGGTGGGAGGATATG | 8816 |
rs767645189 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063977 | CATCAAGTTTGCTAA[C/T]AAACCATAAAAAAAG | 8816 |
rs767655137 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111308 | ACCCAGAGAGAACCT[A/G]AGAGCAATTTCCCGA | 8816 |
rs767686794 | snp | A/G | 1.73673e-05 | 0.00294675 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055635 | AAAATGAAAAACAAA[A/G]GCAACAAGGAGTAAC | 8816 |
rs767713400 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113368 | TAATCAGAACACCAA[A/G]CAACTCTTATCCTTT | 8816 |
rs767759732 | in-del | -/AA | 1.79178e-05 | 0.00299309 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091171 | GCTGGCAGTAAAAAG[-/AA]AAAGAGTCAGCATCT | 8816 |
rs767799579 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146569 | AAGTATAGCAAACCA[C/G]AGGAAAAAAAAATCT | 8816 |
rs767859382 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087609 | TATACTAGAAAGAAA[C/T]AAACTATGTATTTGT | 8816 |
rs767865104 | snp | A/G | 1.6519e-05 | 0.00287388 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69119208 | CCTTTCAACATCATG[A/G]AGGATAACTTGCTCA | 8816 |
rs767926121 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067431 | TCACTGCAACCCCCC[A/G]CTCCCAGGCTCAAGC | 8816 |
rs767945203 | snp | A/C | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090110 | CATGCTCTATTATTC[A/C]ACAAAACAAGAATTA | 8816 |
rs767950273 | snp | C/G | 3.2956e-05 | 0.00405918 | missense | DCAF5 | GRCh38.p7 | 14:69054759 | ATGCCCGGCTTGGTT[C/G]AATCTCTAGCGTGGA | 8816 |
rs767980160 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052813 | AAGTCTGAGGGAAGA[C/T]GCCAGTCCCACCAAT | 8816 |
rs767999304 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086735 | TGTCAACCCAGAGAG[C/G]TTGAGTGGTGATGTA | 8816 |
rs768021246 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | DCAF5 | GRCh38.p7 | 14:69054843 | TCTGGGGGTAATCAT[A/G]GTTGTCTTCTCCAAT | 8816 |
rs768028236 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144311 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCACAGCA | 8816 |
rs768029070 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102896 | ATTATCAAGTGTTAC[A/G]TACTGTACATCATCT | 8816 |
rs768039796 | in-del | -/TCTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085623 | GTAAGGAATATCTCA[-/TCTT]TCTTGTGATGATATA | 8816 |
rs768045811 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139021 | TCAGGTGTGATGGCA[C/T]GTGCTTGTAGTCCCA | 8816 |
rs768109017 | in-del | -/CCTCCCTCGGCCTCA | 4.76701e-05 | 0.00488188 | cds-indel, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153015 | GCTCGCGCCGCCGCC[-/CCTCCCTCGGCCTCA]CGCGCGGCCGCTGCT | 8816 |
rs768111443 | snp | C/T | 1.66504e-05 | 0.0028853 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091667 | GCAGGAGGCAGACAG[C/T]ATTTACCTGGTCACG | 8816 |
rs768135325 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088540 | TTAAAAAGAAGTACA[C/T]GTACTCTGAAGAATA | 8816 |
rs768135625 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151853 | CGAGGCCTACACCGC[C/T]CGGCCGGAGCCCCGG | 8816 |
rs768144289 | snp | G/T | 1.6489e-05 | 0.00287128 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116391 | TTCGAATGTCCCAGA[G/T]TCCCACTCCTTCCTT | 8816 |
rs768158304 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108872 | GTTGCAGTTTTCTAT[A/C]ATACCACCAAAATTT | 8816 |
rs768246248 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122123 | TTCCACAGCTCAATG[A/C]AATACAGGAAGAAAA | 8816 |
rs768249816 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074477 | GCTCAGATAGCTTAA[A/G]TACAAATTTATGGAA | 8816 |
rs768269119 | in-del | -/AT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058538 | AAAGAAAAAAAATAC[-/AT]ATATATATATATGGC | 8816 |
rs768287046 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056439 | AAACTCAGGTCTGCC[C/T]GACTTAAAGGCTTAA | 8816 |
rs768287565 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100684 | ACAAATGGGAAAGTT[A/C]AGTGATCAGAATAGA | 8816 |
rs768340849 | snp | C/T | 1.64993e-05 | 0.00287218 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075306 | CAAAGGTCAACAGAG[C/T]CAGCAATAGCAGTAC | 8816 |
rs768369575 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060914 | TTTTTTTAAGAACAA[A/C]AGAAAATGAAAATTA | 8816 |
rs768386194 | in-del | -/GTT | 3.30447e-05 | 0.00406464 | cds-indel | DCAF5 | GRCh38.p7 | 14:69055249 | CCCCAGGTGGAAGGC[-/GTT]GTCGGCAGACTCATC | 8816 |
rs768394012 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080292 | GGCGCTGCTGATGGT[C/T]AGTGCTTAAGAGGAC | 8816 |
rs768394301 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115581 | GGAAGTTTTTTAATA[C/T]AGCATGGCCAACTTT | 8816 |
rs768437596 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075921 | AAAAGGCATGTTAGC[A/T]AAAACTCAGCAACGA | 8816 |
rs768443879 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060014 | AGGGAGATTTATCAC[A/C]GAAGCATCCCAGAGT | 8816 |
rs768561020 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065007 | ATTAAAGTAACTATC[A/T]GATCTAAAGACTAAT | 8816 |
rs768589597 | snp | A/T | 4.94385e-05 | 0.0049716 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062459 | TTGGTTAACAATAGA[A/T]CGATGCCCTTTCAGC | 8816 |
rs768605482 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052157 | ACACACCAGGCACAT[C/T]TTCTCTTTCACAGAG | 8816 |
rs768621760 | snp | C/T | 1.65108e-05 | 0.00287317 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122316 | TGACCCTGGAGTGGA[C/T]GGCTTGTTCCATGTG | 8816 |
rs768644805 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101821 | TAGGCAACTGTAACA[A/C]AATGGGTAAGTATTT | 8816 |
rs768660424 | in-del | -/AAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133056 | TGCTATTTGAACTCA[-/AAC]AACAGCTAACATCAG | 8816 |
rs768661617 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104305 | TCAAAGTATTTCAAA[A/T]CAAACAGAGAGATAA | 8816 |
rs768683841 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068914 | ATAACTACTTAAGAA[A/G]TGAGAAAAGCCAGAT | 8816 |
rs768709606 | snp | C/T | 1.66407e-05 | 0.00288446 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119282 | CAAGGTGGTCCCTGT[C/T]CACATTACAATTTAG | 8816 |
rs768710108 | in-del | -/GCGGGGAGGC | 3.96999e-05 | 0.00445515 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152727 | GGAGGCTGGGAGGGT[-/GCGGGGAGGC]GCGGGGAGGCGCGGG | 8816 |
rs768727869 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151597 | ATCAGCCGTCTTCAC[A/C]CCCCCTCCCCTGAGC | 8816 |
rs768772314 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148721 | AAAAAAAAAGTAATG[C/T]TCACTCAAAATCAAG | 8816 |
rs768800933 | snp | G/T | 0.0117501 | 0.0757429 | missense | DCAF5 | GRCh38.p7 | 14:69053976 | TATCTGTGGCTGGGG[G/T]GTCAGTGGGGTCCTC | 8816 |
rs768836088 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140082 | ACTAGCCTGGGCGAC[A/G]TAGAGAAATCTCGTC | 8816 |
rs768867064 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132423 | TAAATATCTCAGAGC[A/G]CATCATTCTACAAAC | 8816 |
rs768900348 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125139 | AATATTCTATAGCCC[C/T]GACTCTTAACCACTA | 8816 |
rs768926074 | snp | C/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153688 | TAGGGCCGCACACTT[C/G]GAGGAACGTTGCCTG | 8816 |
rs768926100 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138727 | AAGACTTCTATTAGA[C/T]GATCATTAGTCCTTT | 8816 |
rs768929074 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089508 | ATAAAACTCTTCCCA[C/T]AGGACAAGTCACAAA | 8816 |
rs768951491 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056719 | GACTTCGTTTCCCCA[A/G]AGCTATCTAAGGACA | 8816 |
rs768969231 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096333 | AGGAAGACACATTGC[A/G]ATCTGTGAATGAACA | 8816 |
rs769009110 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100576 | AAGTTTCCCTTGGTT[A/G]GCATTGGACATAGTC | 8816 |
rs769014976 | snp | C/T | 1.6507e-05 | 0.00287284 | missense | DCAF5 | GRCh38.p7 | 14:69054315 | GAGGAGAAGGCGGCT[C/T]CTCAGCCCGACTGCT | 8816 |
rs769031568 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132490 | AAATTCAGTTACCAC[C/T]TTTCTATTCACTCAC | 8816 |
rs769051784 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151084 | GAATACATAAAAAAC[A/G]ACAGCAGGGAAACTG | 8816 |
rs769069023 | snp | C/T | 1.74906e-05 | 0.0029572 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091849 | CGTACACTCATGGCA[C/T]TTTGGAGGGACAGGT | 8816 |
rs769070885 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054825 | AGAGGTCATCCACTT[C/T]GATCTGGGGGTAATC | 8816 |
rs769117600 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135645 | CACCTCAAGGAAAAT[A/C]ATTGGCAGTATTTGT | 8816 |
rs769167222 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083456 | AGTGGAACCTCAAAC[C/T]GCGGCAGTGGAACCT | 8816 |
rs769211949 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061662 | CAATCAGTAGTTTTA[A/T]CCATGCCATATTAGG | 8816 |
rs769219471 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148671 | CTGCACTCCAGCCTG[A/G]GCGACAGAGCAAGAC | 8816 |
rs769277735 | snp | A/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051871 | ATTTTTTTTGTATAT[A/G]AAGGATTAAAAAATT | 8816 |
rs769304455 | snp | C/T | 2.06533e-05 | 0.00321344 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091873 | GACAGGTTTCCACCA[C/T]AGCGCAGGAGAGAAC | 8816 |
rs769368088 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133944 | CAGTGGAGTTTAATA[A/C]AGCTAGGGTTTTGAA | 8816 |
rs769375386 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094037 | TAAACACTGAACTCA[A/G]AAACAATGAGAGGCT | 8816 |
rs769380520 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061575 | TTAGTATTCATACCC[A/G]AGTAGCCTCAATTAC | 8816 |
rs769415839 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113218 | GTGTTCAGGGTGAGA[A/C]CTTCATCACTGCTCC | 8816 |
rs769420998 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122060 | CACACTATCCTAATA[C/T]ATAATACTGCTGTAA | 8816 |
rs769479886 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100312 | AGGGTCCATGGAAGA[A/G]AGCTTTGAGAAAAGT | 8816 |
rs769481083 | snp | G/T | 1.65023e-05 | 0.00287244 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122300 | TTCAGCTGTATGGGC[G/T]TGACCCTGGAGTGGA | 8816 |
rs769481848 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084893 | GACCCTCCGGATGAC[C/T]CTAAGGAATAATATT | 8816 |
rs769501663 | in-del | -/CCG | 0.000611409 | 0.0174737 | cds-indel, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152986 | CTCTTCATGCTGGAA[-/CCG]CCGCCGCCGCCGCTC | 8816 |
rs769507620 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126253 | ACCTCTGCCTCCCGG[A/G]TTCAAGCAATTCTCC | 8816 |
rs769527719 | in-del | -/A | 1.64789e-05 | 0.0028704 | frameshift-variant | DCAF5 | GRCh38.p7 | 14:69062432 | CATGTAGGTGTGGGG[-/A]TTAAATCGGACTTGG | 8816 |
rs769538723 | snp | C/T | 4.94743e-05 | 0.0049734 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054478 | GGGAGTTCTAGGAGT[C/T]TCTTCTTTAAAAGTG | 8816 |
rs769623519 | snp | C/T | 1.65244e-05 | 0.00287436 | missense | DCAF5 | GRCh38.p7 | 14:69054344 | CTCAGGGCCTTTCCA[C/T]TGAGCTTCTTGGTTT | 8816 |
rs769635920 | snp | C/T | 1.65023e-05 | 0.00287244 | missense | DCAF5 | GRCh38.p7 | 14:69055565 | TCGTCCTCAATCCGA[C/T]CGTCGAGGTCTCCAG | 8816 |
rs769700654 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102382 | AAAGTGCTGGGATTA[C/T]GGGCATGAGCCACCG | 8816 |
rs769720957 | snp | C/T | 1.65864e-05 | 0.00287974 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119276 | TTCGTGCAAGGTGGT[C/T]CCTGTCCACATTACA | 8816 |
rs769744396 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064785 | GAACTGGATCTGTCT[A/T]ACCTACTCTTGCATA | 8816 |
rs769749696 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147820 | TTAGTCATAAGCACA[C/T]AAAAAAGATAATAAT | 8816 |
rs769770491 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054819 | AGGAGGAGAGGTCAT[C/G]CACTTTGATCTGGGG | 8816 |
rs769795003 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116183 | CCTCAGCAAGGAGTA[C/T]GGATTTGTCGCTGTC | 8816 |
rs769819260 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082161 | TAACTGGCATATAAT[A/G]CACCTTTGATCATAC | 8816 |
rs769853801 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117212 | TCTGAGCAGGTAAAG[C/T]ACTCAGTCATCTCTG | 8816 |
rs770023090 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130979 | TGTGTGTGGTGAGAT[A/G]ATGTTTGTAAAAGCA | 8816 |
rs770031800 | snp | C/T | 3.29679e-05 | 0.00405991 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054742 | TATGTCAGAAGTTGG[C/T]GATGCCCGGCTTGGT | 8816 |
rs770048229 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104021 | ATGTGAGTAGTTTCC[A/C]GCTTTTGGTTATAAG | 8816 |
rs770065320 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101216 | GATGGATTATTCCAC[C/T]TATTAAAAAGAACAG | 8816 |
rs770071377 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149926 | ACTAGTTTTAAACGT[A/G]GGAAAATTATTGAAG | 8816 |
rs770093444 | snp | A/G | 1.70947e-05 | 0.00292354 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091633 | AGAACAATCAGAAAG[A/G]AAAGCATAAGTGTGA | 8816 |
rs770097958 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109984 | TGTTAACACCTAATA[C/T]TATAAGTCTTTTTAA | 8816 |
rs770117132 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153306 | GCGCCCCTCCCCTCC[A/G]CGGGGGGCTGGCCGG | 8816 |
rs770119196 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058600 | TGAGAAAGAGCCAGG[C/T]GTGGTGGCTCACACC | 8816 |
rs770160949 | snp | C/G/T | 0.00014894 | 0.00862841 | missense | DCAF5 | GRCh38.p7 | 14:69054017 | GCATTGGGGGTCTCA[C/G/T]AGGCCATTTCAGACC | 8816 |
rs770179573 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054181 | ACGAGGGTGTAAGCG[C/T]CCATTGTTGTGGTTG | 8816 |
rs770205983 | snp | C/T | 5.12046e-05 | 0.00505961 | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091061 | AGTATATTCTTAAAC[C/T]GCCAGCTTTAAGTCA | 8816 |
rs770210920 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095110 | TATACTCCTGTCCTC[A/C]ACACATTCCCTGAAG | 8816 |
rs770258255 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074094 | TTATGCCAAAAGTAG[A/G]CCCCAACAGGTTTTG | 8816 |
rs770265359 | snp | A/G | 1.65002e-05 | 0.00287225 | missense | DCAF5 | GRCh38.p7 | 14:69055287 | TGGGAGGCGGGGAGC[A/G]AGGCAATGAGGCCGA | 8816 |
rs770265811 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | DCAF5 | GRCh38.p7 | 14:69054110 | TGTCCTGGGGAAGAG[C/T]AGGCCACCACCTCCA | 8816 |
rs770295634 | snp | C/T | 3.49546e-05 | 0.00418044 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152951 | CCACTGACCTCATGC[C/T]GCCCCCCAGGCCAGC | 8816 |
rs770304157 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098895 | GAGACTCTGTCTCCA[-/AA]AAAAAAAAAAAAAAA | 8816 |
rs770323157 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064575 | AAGAGTTTGAATAGG[A/T]ATGGAGTTAGAAGCT | 8816 |
rs770400188 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129582 | CTAGTCAGTTCAGAA[A/T]GGCAGAGATTTATTG | 8816 |
rs770483830 | snp | A/C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143479 | GTTACATATGCCTGG[A/C/G]ACATGAAATGCCCCC | 8816 |
rs770491059 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084802 | GTTCTGCAATGCAGA[C/T]TCAGGAACACTATTG | 8816 |
rs770504201 | in-del | -/CGCCGCCGCCGCTCG | 2.8939e-05 | 0.00380377 | cds-indel, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152990 | TCATGCTGGAACCGC[-/CGCCGCCGCCGCTCG]CGCCGCCGCCCCTCC | 8816 |
rs770505725 | snp | A/G | 1.65165e-05 | 0.00287367 | missense | DCAF5 | GRCh38.p7 | 14:69054324 | GCGGCTCCTCAGCCC[A/G]ACTGCTCAGGGCCTT | 8816 |
rs770512577 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098098 | AAGGCCCTAGACAAT[A/T]CCCCCTACCCTCATC | 8816 |
rs770538479 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063641 | CACTCATTCCAAATA[C/T]TTCTCAATGTCTGTG | 8816 |
rs770545547 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133748 | CCATGTCTCTAATGA[A/G]GTAAGTAGAACAGAA | 8816 |
rs770562435 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124864 | CTTCTGCTACTATAT[A/T]TTTTTTTAATTAGAT | 8816 |
rs770574982 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083322 | AGAGTTATAAATGGC[C/T]GATTTAATAAAGTTA | 8816 |
rs770637638 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118637 | CTTTAAAGCAGCCAA[C/G]TCTGATGCCTACAGG | 8816 |
rs770682014 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | DCAF5 | GRCh38.p7 | 14:69055547 | GTATAGAGGCAGCGG[A/G]AATCGTCCTCAATCC | 8816 |
rs770771790 | snp | C/T | 4.9689e-05 | 0.00498418 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119263 | AGACATCTGATCATT[C/T]GTGCAAGGTGGTCCC | 8816 |
rs770821356 | snp | A/G | 4.94189e-05 | 0.00497062 | missense | DCAF5 | GRCh38.p7 | 14:69054794 | CTCCGCTCAGGGGAC[A/G]AGGTTGGGGAGGAGG | 8816 |
rs770867181 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69139925 | AGAGAAGGAAGGAAA[A/G]AAGGAAGGGAGGGAG | 8816 |
rs770886104 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126053 | AATTTGAAATATAAA[A/G]TATTTAGGTATAAAT | 8816 |
rs770913471 | snp | A/C | 9.90181e-05 | 0.00703557 | missense | DCAF5 | GRCh38.p7 | 14:69054705 | ACTTGTAAGCTTTAT[A/C]AATTTTTCGCTCAAC | 8816 |
rs770916306 | snp | G/T | 8.70284e-05 | 0.00659596 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091011 | CTGACACTTCAGAAC[G/T]TCTATGGTTAAGACA | 8816 |
rs770942350 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114580 | TGTAGTTACCTCTGG[A/G]GTGACTACAGACACT | 8816 |
rs770961332 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093341 | GATCCCAGTAGTTTT[A/G]GAGAAAAAAGTTTAT | 8816 |
rs771007887 | snp | C/T | 5.17647e-05 | 0.00508721 | synonymous-codon, upstream-variant-2KB, splice-donor-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152943 | GAAGCCCACCACTGA[C/T]CTCATGCTGCCCCCC | 8816 |
rs771078177 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143332 | AAAACATTCAGACCC[A/C]ACCTGGAAATCTAGC | 8816 |
rs771097066 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080354 | CTTACAAATATTTGC[A/T]GTGGGATACAAGGAA | 8816 |
rs771125980 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116031 | CCCCTCCACCCACCC[C/G]ACACCAAGAGCTCCT | 8816 |
rs771159788 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148869 | AAATCAAACACTTTG[G/T]GACTGGTAGAGCCTC | 8816 |
rs771203698 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072840 | ATACAGAGAAAACAA[A/C]CCCTCAATTACAGTG | 8816 |
rs771221190 | snp | A/G | 1.66687e-05 | 0.00288688 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152796 | GCCTCCATTGTTGGA[A/G]AATTCAATGGCATTG | 8816 |
rs771227013 | snp | A/T | 1.65471e-05 | 0.00287633 | missense | DCAF5 | GRCh38.p7 | 14:69054014 | CCAGCATTGGGGGTC[A/T]CACAGGCCATTTCAG | 8816 |
rs771235479 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69055673 | TATTCTTTCACTGGT[-/G]GTGATAAAGAACACC | 8816 |
rs771257178 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057207 | AGAATAAAATAAAGG[A/G]TTTATCTGAAGGTTT | 8816 |
rs771266367 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054082 | GGACGAGTTATCACG[A/G]TCAGTGTCTGAGTGT | 8816 |
rs771268238 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107875 | TTTACTAAGTTTCCA[C/T]AATATTCCAAGCACT | 8816 |
rs771295205 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081785 | GTGTGTGTTTGTGGT[A/G]CGTGCTTACACAGGA | 8816 |
rs771295253 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065753 | TGAAATAGCTAAAGT[C/T]AAAATGCCAATATCA | 8816 |
rs771300674 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072505 | CCTAGATACTTGGGA[A/G]GCTTAGGCAGGAGGA | 8816 |
rs771306732 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141646 | AATCAGGATAAATGA[C/T]TGGCTTGGTTACAAA | 8816 |
rs771380794 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085983 | ACAATTCGATTTGCC[A/G]TTTCACACTACTGTC | 8816 |
rs771422225 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153933 | TCCCGAGAAGCACGA[A/G]GTACTTCTCTCCGTT | 8816 |
rs771423124 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111840 | TTTTATCCAGTCACC[C/T]ACACTCAAGCCTCTC | 8816 |
rs771453112 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058461 | GAGGAAAAGGTTGCA[C/G]TGAGCCGAGATCGCG | 8816 |
rs771568555 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153371 | GCCGGCTGCTTTCCC[A/G]GTTGAGCCGCTTCCC | 8816 |
rs771580163 | snp | A/C | 3.31192e-05 | 0.00406921 | missense | DCAF5 | GRCh38.p7 | 14:69055229 | GTGGTGGTGACCCGC[A/C]GGGGCCCCAGGTGGA | 8816 |
rs771603059 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131469 | AGTGGATGGAAAATA[A/C]GTCTGTTTTGTTATT | 8816 |
rs771677566 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061995 | CCCTGTCTCTAAAAA[A/C]ATTTTTTTAATGAAA | 8816 |
rs771679847 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146170 | TCTTGCTCTCTTTAG[G/T]AAATCTTAGCTATCA | 8816 |
rs771682257 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083834 | AAACAGAAAATAATG[A/T]TGAGAAGCCAGATGA | 8816 |
rs771748682 | in-del | -/TTTTTTTTTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067353 | TTTTTTTTTTTTTTT[-/TTTTTTTTTG]AGACAGGGTCTCACT | 8816 |
rs771751275 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124622 | GTTCTCTGGCCTAGG[A/G]TAGTATCTAAATTAT | 8816 |
rs771768107 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144789 | TCCAGAAAATGTGAC[C/T]TGCCTACAAAGGGAA | 8816 |
rs771792805 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69149690 | AACTATGAACAATCT[A/G]TCATTTTAATCACAG | 8816 |
rs771884269 | snp | C/T | 1.65151e-05 | 0.00287355 | missense | DCAF5 | GRCh38.p7 | 14:69054683 | GAGATATAAGAGTAG[C/T]GGAGCCACTTGTAAG | 8816 |
rs771892630 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102220 | TTCAAGTGATTCTCC[C/T]GCTTCAGCCTCCTGA | 8816 |
rs771909285 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074762 | GTGTGGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 8816 |
rs771969463 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052209 | TTTGGCTTAAACCAA[C/G]CACCTTGTGTTTATA | 8816 |
rs771972517 | in-del | -/AGAGCTGCT | 1.64734e-05 | 0.00286992 | cds-indel | DCAF5 | GRCh38.p7 | 14:69054982 | CTCCTCCTCATCCTC[-/AGAGCTGCT]AGAGCTGCTGGAACT | 8816 |
rs771995206 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110075 | GAGTGATAAAGTTCA[A/G]TACTTTTCAAATGCT | 8816 |
rs772016964 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136420 | AGCACCCAGCCTATA[A/G]TTTTCTTTATATACT | 8816 |
rs772049063 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088010 | TTTAAAACCAAGAGA[C/T]CTTACATAAAAATCT | 8816 |
rs772063805 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066777 | TTATGGCCCACTTTC[A/C]TAACATTCAGCCAGG | 8816 |
rs772066428 | snp | A/G | 3.29815e-05 | 0.00406075 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075322 | CAGCAATAGCAGTAC[A/G]TTCATGTGAAGGATA | 8816 |
rs772074971 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140259 | GCGACAGAATGAGAC[C/T]CTGTCTAAAAAAAAA | 8816 |
rs772111707 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056995 | AGAGTTTCAAGGGAT[G/T]GGTTTTCACTTTGGA | 8816 |
rs772127004 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123435 | ATTTGCATAGCCCTA[A/T]CTAGATGGCTATAAA | 8816 |
rs772130640 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141281 | TTTTGGTTTTACTTG[C/G]ATACCAGACAGTGCA | 8816 |
rs772169672 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058295 | AGGCCGTGGCGGGTA[G/T]ATCACTTGAGGTCAG | 8816 |
rs772224630 | snp | A/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154538 | TATAAAAGTACATAT[A/T]CTAGCAAACATTACT | 8816 |
rs772239613 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091038 | GACAGAAAGGTGCAA[A/G]AAGGCCAAGTATATT | 8816 |
rs772248438 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133690 | TACCTAGTACCCTTC[-/T]GCTAAAAGCTGAGTC | 8816 |
rs772326312 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | DCAF5 | GRCh38.p7 | 14:69054926 | TTCTGTCGGCGCCGC[A/G]TGGCATTCCGCTGCC | 8816 |
rs772329467 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089573 | AAAAGCCATTCAATA[A/C]TTTTATAATTATATA | 8816 |
rs772329511 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107503 | AAGCTCCTCAGGTGA[C/T]TCTGATGCCCCTTAA | 8816 |
rs772351621 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078982 | ATTTTCATGCCTCAG[A/C]CTCCCCAGCAGCTGG | 8816 |
rs772384748 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084581 | GTGGATGGTCTTGAG[C/T]AGGGATATGTTGTTT | 8816 |
rs772386770 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069135 | AGGCCTAAGTCACTG[A/C]GAGTGAATACATGTC | 8816 |
rs772390014 | snp | C/T | 8.27452e-05 | 0.00643162 | missense | DCAF5 | GRCh38.p7 | 14:69054006 | CTCTTGTTCCAGCAT[C/T]GGGGGTCTCACAGGC | 8816 |
rs772392493 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | DCAF5 | GRCh38.p7 | 14:69055064 | AGATCTGTGTCTAGT[A/T]CCACCTCACAGACAT | 8816 |
rs772421028 | in-del | -/AAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098894 | CGAGACTCTGTCTCC[-/AAA]AAAAAAAAAAAAAAA | 8816 |
rs772428985 | snp | A/G | 4.95536e-05 | 0.00497738 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119173 | AAGTCAATCACCTTC[A/G]CACACCACCAATCTA | 8816 |
rs772436176 | snp | A/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153881 | GAGAAAGGGATAAAG[A/T]AGTAGGAAGAAAATT | 8816 |
rs772456688 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120794 | GTATATAAAAAGAAT[A/G]AGATTCTACTCTGTC | 8816 |
rs772474067 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083483 | ACCTAAAGTTGCAGG[A/G]GGCCTCAAATCTGAC | 8816 |
rs772485892 | snp | C/T | 1.66932e-05 | 0.002889 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116337 | GAGGCAGAGGAAAGT[C/T]TTAACACCTATGAAT | 8816 |
rs772520796 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132706 | TATTTTAGAGGTGAT[A/G]TAATGTGGGGCAGCA | 8816 |
rs772550140 | snp | C/T | 1.95907e-05 | 0.0031297 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152973 | CAGGCCAGCTCTCCT[C/T]TTCATGCTGGAACCG | 8816 |
rs772576745 | in-del | -/AGTAAATAGGTTCC | 1.66269e-05 | 0.00288326 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062558 | GATGAAATGAATGAA[-/AGTAAATAGGTTCC]AGTAATGGCAGATAA | 8816 |
rs772584285 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070538 | AGAATCAGACATGTA[A/G]TTAGTGGTAGTTAAG | 8816 |
rs772595035 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | DCAF5 | GRCh38.p7 | 14:69054207 | GGTTGGCACAGATGG[C/T]TTCGAGGCTCCTCTC | 8816 |
rs772611793 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095777 | GATTACTATAAATCC[A/G]TGATTAACTAATCCA | 8816 |
rs772632286 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062251 | TCTAATATTTTGTAA[C/T]ATGTTAAAATCTGAG | 8816 |
rs772679236 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111453 | TGAGTGGGGAAAAAA[A/C]CACTCTCTTTATTAT | 8816 |
rs772774633 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144224 | AGAAGGCCTGGCATA[C/T]GTTACAAGATAAAAA | 8816 |
rs772797747 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082640 | TGAGGGGCCATTAAC[C/T]ATTAGCCCCCCTCCA | 8816 |
rs772851062 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111869 | TCCTCCCCAGTGACC[A/G]CTCATCACCACTAAA | 8816 |
rs772864002 | snp | C/T | 4.94385e-05 | 0.0049716 | missense | DCAF5 | GRCh38.p7 | 14:69054144 | CCCCCAAGTTCTGCC[C/T]GTTATTGTGAGGGTG | 8816 |
rs772897101 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146214 | ATAAATCAAATTAAA[A/G]ATGATCCTTTGAACA | 8816 |
rs772957826 | in-del | -/CCG/CCGCCG | 0.00130188 | 0.0254865 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152985 | CTCTTCATGCTGGAA[-/CCG/CCGCCG]CCGCCGCCGCCGCCG | 8816 |
rs772960913 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131594 | CCTTTTTCTAGACAC[A/G]TATCAGAGAGGTAAA | 8816 |
rs772973455 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096402 | CTCTGGCTTGATATA[C/T]AGATGAATTCAGTAT | 8816 |
rs773002687 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087296 | GAAGTGTATGAAGCT[A/T]AGAAGACAGAATGTA | 8816 |
rs773003666 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076117 | AGGATGACTATTACC[A/C]AAAAAAAAAAAAATT | 8816 |
rs773035487 | snp | C/T | 1.66463e-05 | 0.00288494 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118308 | AGCAAGACAGAGGCA[C/T]ACACATACACACAAG | 8816 |
rs773043527 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117341 | AAACAAGCTTCTCTT[-/A]TAGCCTGAACCTAAA | 8816 |
rs773101970 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053739 | ATCAGACACAAAATT[G/T]CAGGCCCTGGTTTCA | 8816 |
rs773112509 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081479 | AAGAGGGCAAGCTAT[G/T]TACTGATCTGAATGT | 8816 |
rs773121592 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118194 | GCCATCATCTGAGGA[A/G]CTGGCAAAAATGTTG | 8816 |
rs773141798 | snp | C/T | | | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122273 | CAAAAAATGTTGGAA[C/T]GGTGCTCTCCTTTCA | 8816 |
rs773153795 | snp | C/G/T | 0.00099336 | 0.0222647 | missense | DCAF5 | GRCh38.p7 | 14:69054600 | TGTCTTTGTGGCTGG[C/G/T]TCCTGCTCTCCCTTC | 8816 |
rs773247873 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69075355 | CTTGCCTGCTTCTGG[A/G]TCTGCAGGAATTCTC | 8816 |
rs773267655 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099566 | CTTTAAGTGAGTTAA[A/G]TTCATCCATGTGCTA | 8816 |
rs773268939 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074771 | GGGTGCGGTGGCTCA[C/T]ACCTGTAATGCCAGC | 8816 |
rs773275247 | in-del | -/AAAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072624 | CGAGACCCTGACTTT[-/AAAA]AAAAAAAAAAAAAAA | 8816 |
rs773276601 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126769 | GTAAGTATAATCAAC[A/T]GATCTTTGACCACGG | 8816 |
rs773285996 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065017 | CTATCAGATCTAAAG[A/G]CTAATTGAAGGCTAT | 8816 |
rs773314704 | snp | G/T | 1.65507e-05 | 0.00287664 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122363 | CGGTCATCTCCTCCT[G/T]AAGAAGGAAATAAGA | 8816 |
rs773334863 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123441 | ATAGCCCTATCTAGA[C/T]GGCTATAAAAGAAGC | 8816 |
rs773336053 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099088 | AAACCCAGTCTCTAC[C/T]AAAAATTTAAAAAAT | 8816 |
rs773340451 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | DCAF5 | GRCh38.p7 | 14:69062488 | GCACCATGAAGGCTC[C/T]GTTGACCACCCTACC | 8816 |
rs773364218 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077895 | GAAAATGCTATCTAT[A/C]GGGATTAGGTAATCA | 8816 |
rs773397137 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135982 | AGAAATTATTCGATA[C/T]GGTTTTATATTCTAC | 8816 |
rs773416731 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151942 | CTGGGCGAGAGGGAG[A/G]AGAAGCAGAGACCAC | 8816 |
rs773438845 | snp | C/T | | | intron-variant, synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091064 | ATATTCTTAAACTGC[C/T]AGCTTTAAGTCAACA | 8816 |
rs773441355 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | DCAF5 | GRCh38.p7 | 14:69055067 | TCTGTGTCTAGTTCC[A/G]CCTCACAGACATTCT | 8816 |
rs773455822 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119404 | TTAAGAAGGATAGGA[C/T]ATTCTTACAGAGAAT | 8816 |
rs773477027 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113427 | GTAAAAACTTTCTAC[C/T]ATCCCTAGAAAAAAT | 8816 |
rs773499953 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070699 | CCTTCCTACCTACTT[C/T]AGAGGTCTTAGACAT | 8816 |
rs773510262 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148184 | ATAAGAGGAGGCAAT[A/G]AGAGCAATTTAGAGT | 8816 |
rs773589581 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069148 | TGAGAGTGAATACAT[G/T]TCTAGAAAAAGAAGA | 8816 |
rs773616880 | snp | A/C/T | 6.61828e-05 | 0.00575219 | missense | DCAF5 | GRCh38.p7 | 14:69054012 | TTCCAGCATTGGGGG[A/C/T]CTCACAGGCCATTTC | 8816 |
rs773635299 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079000 | CCCCAGCAGCTGGGA[C/T]TACAGGCGGGCACCA | 8816 |
rs773686250 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151528 | GTTCCCCCTTCATCC[C/G]TCCCAATATAGGAAA | 8816 |
rs773696030 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057055 | TAATGTTGATTCCTC[A/C]GTCCCACTCTTAGAG | 8816 |
rs773706463 | snp | A/T | 5.30218e-05 | 0.0051486 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053852 | TTGTTTTCCCTTTGT[A/T]TTTATCATGTTTTTA | 8816 |
rs773793075 | snp | C/T | 1.6522e-05 | 0.00287414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118130 | CAGTCATTTGCACAG[C/T]GAGCCTACCTCCATG | 8816 |
rs773795812 | snp | C/T | 2.0356e-05 | 0.00319024 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091871 | GGGACAGGTTTCCAC[C/T]ATAGCGCAGGAGAGA | 8816 |
rs773807597 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144621 | GGTACTCAATAAATA[C/T]TTTAATGAGTAAATA | 8816 |
rs773809581 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081736 | TCCTCTGTCAATCCA[C/T]TGACCTTTATAGAAA | 8816 |
rs773822684 | snp | C/T | 1.65466e-05 | 0.00287628 | missense | DCAF5 | GRCh38.p7 | 14:69054021 | TGGGGGTCTCACAGG[C/T]CATTTCAGACCCGCA | 8816 |
rs773824486 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147377 | CAGTTGCAGCAGCAG[G/T]AGCAACAGCATGGGT | 8816 |
rs773825051 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089608 | CTGAAAGACAGAAAC[A/G]ATGATATCTTTGATG | 8816 |
rs773841845 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070263 | AATATAAATATTTTC[-/AA]GAGACACCTACCAAC | 8816 |
rs773885520 | in-del | -/TTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067340 | CCGATTTCGTATCTT[-/TTTTTTTTT]TTTTTTTTTTTTTGA | 8816 |
rs773886626 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072627 | GACCCTGACTTTAAA[-/A]AAAAAAAAAAAAAAA | 8816 |
rs773908699 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114530 | TAGTCGTATATACAT[G/T]ACATTAAGTTCTGGA | 8816 |
rs773910626 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | DCAF5 | GRCh38.p7 | 14:69055119 | AAAGGGCCAGGAGGC[A/G]TTTGTCTTGGTAGCG | 8816 |
rs773912797 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150815 | GAGGTTAGCTTGAGC[C/G]TGGGAGATCAAGGCT | 8816 |
rs773915123 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105442 | TGTCAACTTGACTGG[A/G]CTCAGGCATGCCTAC | 8816 |
rs773920272 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123304 | CTTGTCAGTTTTGTT[A/C]ACTGGGAAATACCTG | 8816 |
rs773998740 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129952 | GTTGGTTTCATTCTG[C/T]ACTAAAATCACTAAT | 8816 |
rs774027289 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059093 | AAGTGATCATGATAC[A/G]CTTTTATTTTTGGGA | 8816 |
rs774029048 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074490 | AAATACAAATTTATG[A/G]AAAGTTGCAGCCTTT | 8816 |
rs774055629 | in-del | -/CATT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147122 | GAAACAGGAAATGAC[-/CATT]AATTAATAGGTTCAA | 8816 |
rs774057846 | in-del | -/CGCCGCCGCCGCTCG | 2.8939e-05 | 0.00380377 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152989 | TCATGCTGGAACCGC[-/CGCCGCCGCCGCTCG]CGCCGCCGCCGCTCG | 8816 |
rs774076452 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143704 | GGGAAGCTTATATTA[C/T]AATGGCAGTGGCGAC | 8816 |
rs774076811 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083642 | TGGAAAATATAAAAG[C/T]TAAAAAATCTCCCCA | 8816 |
rs774101845 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | DCAF5 | GRCh38.p7 | 14:69054494 | TCTTCTTTAAAAGTG[G/T]CCTTGCTGCAGCCTT | 8816 |
rs774107790 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122155 | TAAGGAGTTATTTTC[A/G]CACTCTTTTCTCTAA | 8816 |
rs774109345 | in-del | -/TG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121935 | ATATGTGTGTGTGTC[-/TG]TGTGTGTGTTTCTGT | 8816 |
rs774134211 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087247 | GGCATTCTTTTTTAA[C/T]CCTATTAAGAGACTC | 8816 |
rs774142029 | snp | G/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052185 | GAGCTTATCAGGATG[G/T]TATCTCCTTTTGGCT | 8816 |
rs774165495 | snp | C/T | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050496 | TTTGCTTTTTTTTTT[C/T]TTAGAAAAAAGTTTG | 8816 |
rs774193026 | snp | G/T | 0.000131974 | 0.00812217 | missense | DCAF5 | GRCh38.p7 | 14:69054584 | GAAGAAGGGGCTGGG[G/T]TGTCTTTGTGGCTGG | 8816 |
rs774209618 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100807 | GTAAAAGAAGCCAAG[A/G]TTATTATTGAGAGTA | 8816 |
rs774281164 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148743 | AAAATCAAGTTCATA[A/C]AGCACCTTCACATAT | 8816 |
rs774304517 | snp | C/T | 9.88859e-05 | 0.00703087 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062465 | AACAATAGATCGATG[C/T]CCTTTCAGCACCATG | 8816 |
rs774407921 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073191 | CTATTTTTTAAGGAA[C/T]TACTAAATAAACTTA | 8816 |
rs774415335 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086396 | AACAAAAAAACATAA[C/T]AGTGGATATGAAAAT | 8816 |
rs774468788 | snp | C/T | 5.09584e-05 | 0.00504744 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055617 | GGCTCCAGATCTGAA[C/T]AGAAAATGAAAAACA | 8816 |
rs774471291 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136189 | GGGGCAGTCATAGCT[C/G]ACTGCAGCCTCAACC | 8816 |
rs774481863 | snp | A/C | 1.65179e-05 | 0.00287379 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122179 | TCTCTAAAATCCCAA[A/C]CACAGTGACGTTCCC | 8816 |
rs774505073 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088404 | TCTACAGTGGTGGCA[A/G]TGAGCATGAGGGAGA | 8816 |
rs774507221 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089527 | ACAAGTCACAAATAA[C/T]AAATTAGTCAAATCT | 8816 |
rs774508458 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126316 | ACACCCACCACCACG[C/T]CCAGCTCATTTTGTA | 8816 |
rs774553644 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125094 | TCACACAATAAAGTC[-/A]ATTGAGCTAAGATTC | 8816 |
rs774575079 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131284 | TTAACTGTGAAGCCT[A/C]AAGGAAAATCATTCA | 8816 |
rs774584733 | snp | C/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154073 | TTGGACAGCTGTTAA[C/G]CAGCAGCTGCGCTCC | 8816 |
rs774589879 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105296 | CATATATGTATAATG[C/T]ATATATAATAGAATA | 8816 |
rs774596096 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125140 | ATATTCTATAGCCCC[A/G]ACTCTTAACCACTAT | 8816 |
rs774604566 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140104 | AATCTCGTCTCTACT[A/G]AAACTACAAAAAATT | 8816 |
rs774623744 | in-del | -/C | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090537 | AACATTCTCATCTAT[-/C]TACACGCAAGACAAT | 8816 |
rs774632966 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083458 | TGGAACCTCAAACTG[C/T]GGCAGTGGAACCTAA | 8816 |
rs774650930 | snp | A/G | 1.88738e-05 | 0.0030719 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053832 | AAGGCTACTTTTGTA[A/G]CTTTTTGTTTTCCCT | 8816 |
rs774718896 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082426 | TCTTTCAGTTTATTA[A/G]AATAACCAACCTTTA | 8816 |
rs774725951 | snp | C/T | 7.38307e-05 | 0.00607535 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091084 | TTAAGTCAACATCAG[C/T]ATCTCCATTCCTGGT | 8816 |
rs774739152 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | DCAF5 | GRCh38.p7 | 14:69054924 | TCTTCTGTCGGCGCC[A/G]CATGGCATTCCGCTG | 8816 |
rs774752539 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150167 | GGAGGAGCGATGGAA[C/T]AGCCTGCTGATAGGA | 8816 |
rs774826567 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054828 | GGTCATCCACTTTGA[G/T]CTGGGGGTAATCATA | 8816 |
rs774828694 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123656 | CCAAACTGAAATACT[-/A]GTACCCAATAAACAA | 8816 |
rs774840167 | snp | A/G | 5.09905e-05 | 0.00504902 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091645 | AAGAAAAGCATAAGT[A/G]TGAGATGCAGGAGGC | 8816 |
rs774920281 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122480 | CAACTCCATAAGATT[C/T]GCATGGAGCACAAAA | 8816 |
rs774942121 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058632 | GTAATCCCAGGACTT[C/T]GGGACGTCAAGGCAG | 8816 |
rs774946158 | in-del | -/TTGAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085447 | GATTCTTTTCCTCCC[-/TTGAT]TTAACAGGATTTTTG | 8816 |
rs774963557 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104444 | AATTCATGGGAAAAA[C/T]CTGAGTCAGAGGAAT | 8816 |
rs774974508 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121353 | GAGAGGCTTTCAAGA[C/T]AGACCTGACAGGACT | 8816 |
rs775024854 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094367 | TGCAGTCTGATCACA[C/G]TATAGGAATTTGGTT | 8816 |
rs775037849 | snp | C/G | 2.10888e-05 | 0.00324715 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091875 | CAGGTTTCCACCATA[C/G]CGCAGGAGAGAACTG | 8816 |
rs775049440 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117472 | CAGCTGTGATCATTA[C/T]AATCTGCACTAAAGG | 8816 |
rs775070228 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072985 | GATCATGGGTTCTGT[A/G]GCCTCTAAAAAAGCT | 8816 |
rs775080946 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108478 | AGACGGAAATGGGTA[C/T]GAAATGGGGTAGGGA | 8816 |
rs775191478 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058610 | CCAGGCGTGGTGGCT[C/T]ACACCTGTAATCCCA | 8816 |
rs775207467 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064799 | TTACCTACTCTTGCA[C/T]ACCTAGAACCTGGGG | 8816 |
rs775224716 | in-del | -/AAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134570 | CAGGGTTAACTAGGG[-/AAT]AATCTCAAGAGAAAT | 8816 |
rs775231039 | snp | A/G | 3.30066e-05 | 0.00406229 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055567 | GTCCTCAATCCGACC[A/G]TCGAGGTCTCCAGTA | 8816 |
rs775232890 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133969 | TTTGAAATACTAACC[C/G]TAGACAATGTCTCTA | 8816 |
rs775242749 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155352 | GCATAAAAATAGACC[A/G]GCATCTGGTCACATG | 8816 |
rs775285182 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098896 | AGACTCTGTCTCCAA[-/A]AAAAAAAAAAAAAAA | 8816 |
rs775307502 | snp | C/T | 1.64901e-05 | 0.00287137 | missense | DCAF5 | GRCh38.p7 | 14:69054483 | TTCTAGGAGTCTCTT[C/T]TTTAAAAGTGTCCTT | 8816 |
rs775326844 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69146536 | AAATCTCACAGGCAA[A/G]AGCATTTTTGCTGTA | 8816 |
rs775361853 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113251 | GGAGATTATCTGTTT[C/T]TAGGACAGCAGGCCC | 8816 |
rs775397480 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137103 | AGTTGTTTAAATTAT[A/G]AATGGGTGGGAGGCC | 8816 |
rs775418198 | snp | C/G | 8.26194e-05 | 0.00642673 | missense | DCAF5 | GRCh38.p7 | 14:69054352 | CTTTCCATTGAGCTT[C/G]TTGGTTTCAAAAGGG | 8816 |
rs775434092 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117282 | AGCCCACAGTGACTC[A/G]ACCACAGCTGCTACT | 8816 |
rs775515451 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123574 | AGTGTACAATTCAGT[A/G]GCATTAAGTACATTT | 8816 |
rs775520854 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150112 | AAAACTCTATGTTCA[A/G]GGAACAAATAGGAAA | 8816 |
rs775527263 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132998 | AGACTTGGCCCAGTG[C/T]CTGATACATATTAAG | 8816 |
rs775540768 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085014 | CTGAAATGATCCAAG[G/T]TTCCATTAAGTGAAT | 8816 |
rs775564421 | in-del | -/AGGTGATCCA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095425 | CAAGAACAGGGTAGG[-/AGGTGATCCA]AGGTGATCCAAAAGA | 8816 |
rs775595255 | snp | C/G | 3.29647e-05 | 0.00405971 | missense | DCAF5 | GRCh38.p7 | 14:69054747 | CAGAAGTTGGTGATG[C/G]CCGGCTTGGTTGAAT | 8816 |
rs775599655 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137535 | CATAATAAAGCTTTC[C/T]TGTCTCTTCTTTGGC | 8816 |
rs775609446 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129591 | TCAGAAAGGCAGAGA[C/T]TTATTGTTTAGTTCC | 8816 |
rs775629913 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104205 | ATACCATTACATATT[C/T]CCACCAGCAATATGT | 8816 |
rs775655561 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088214 | AACAAGTTGTGATCA[C/T]TTGTACAGTGAAAAG | 8816 |
rs775666339 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067009 | CACTGTCCTCAATAC[C/T]ACTTCCCGTCTTCCT | 8816 |
rs775680530 | in-del | -/TC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123699 | GTGCCTAGTCACTGT[-/TC]TTTTTTTTTGAGACG | 8816 |
rs775714977 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151270 | AGAAAACGATCTGGG[A/G]TACAAAAGTCAAGTC | 8816 |
rs775717416 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138566 | TGAGCAAGTCCTTTT[G/T]AAATGCAGAACCTCA | 8816 |
rs775849779 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093601 | ATGGGAAGGGAAGCC[A/C]TGAAACCACAGTACA | 8816 |
rs775880367 | in-del | -/ACC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69076796 | TGTTATGTATATTTT[-/ACC]ACAATTAAAAAAAAA | 8816 |
rs775886213 | snp | A/C | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090726 | TTTTATATTTCTTTT[A/C]TGCCAAAAATAACTC | 8816 |
rs775924245 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080728 | AACATAGTAGAAAAA[A/T]TGGTTACCCAAAATT | 8816 |
rs775927543 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144343 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACAAGG | 8816 |
rs775964021 | snp | A/C | 0.000346166 | 0.0131515 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091063 | TATATTCTTAAACTG[A/C]CAGCTTTAAGTCAAC | 8816 |
rs775985623 | snp | C/T | 1.66208e-05 | 0.00288273 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091669 | AGGAGGCAGACAGCA[C/T]TTACCTGGTCACGAT | 8816 |
rs776003275 | snp | A/C | 1.64792e-05 | 0.00287042 | missense | DCAF5 | GRCh38.p7 | 14:69054114 | CTGGGGAAGAGTAGG[A/C]CACCACCTCCAGCTC | 8816 |
rs776015821 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116190 | AAGGAGTACGGATTT[A/G]TCGCTGTCTATTCCT | 8816 |
rs776143702 | snp | A/G | 1.66073e-05 | 0.00288156 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152823 | ATTGACACAGCCGAA[A/G]TGGCCGAGGAGGTCC | 8816 |
rs776291516 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098127 | TCCTTTATGTCTGTG[A/C]CCCCACCTCCTAGGA | 8816 |
rs776302555 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133806 | TGAGGTCCTGGCTTG[C/T]CTTAGCTCCTAGCTA | 8816 |
rs776337244 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077467 | TTGCTCACTGCAGCC[A/T]CGACCTCCTGGGCTC | 8816 |
rs776343599 | snp | C/T | 1.6886e-05 | 0.00290564 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118326 | ACATACACACAAGCA[C/T]AGTGCAGAGTCCCAG | 8816 |
rs776355608 | snp | A/G | 1.65198e-05 | 0.00287395 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054333 | CAGCCCGACTGCTCA[A/G]GGCCTTTCCATTGAG | 8816 |
rs776363629 | snp | C/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153988 | AAGCGTGATTTGAAA[C/T]TAACGATATATGTTA | 8816 |
rs776368784 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074587 | CAAAGCCCCAGGGAA[-/C]ATACCTGTCCATCAA | 8816 |
rs776368849 | snp | C/G | 6.59337e-05 | 0.0057413 | missense | DCAF5 | GRCh38.p7 | 14:69054214 | ACAGATGGTTTCGAG[C/G]CTCCTCTCCTCACTG | 8816 |
rs776416643 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063715 | AATATGGCTCTAGGG[A/G]TATCTTCTGCTTTTG | 8816 |
rs776423571 | snp | C/G | 0.000197769 | 0.00994209 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062474 | TCGATGCCCTTTCAG[C/G]ACCATGAAGGCTCCG | 8816 |
rs776461653 | in-del | -/ACA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69126792 | GACCACGGAGCAAAG[-/ACA]AAACAATGGAGCAAA | 8816 |
rs776565225 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129447 | CTGCTTTTCACCCAG[C/T]AGAGGGCGCTAAACA | 8816 |
rs776621504 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110519 | GTGATCCAACTGCCT[C/T]GGCCTCCCACAGTGC | 8816 |
rs776649469 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145135 | CAATCCTCCCACCTC[A/G]GCCTCCTGTGTAGCT | 8816 |
rs776710795 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118225 | TCATTCACTGGGCTC[A/G]CAGACAAGCCATATA | 8816 |
rs776727396 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081290 | TACAATTAGATCAGC[A/G]TGGAAGATATATTTA | 8816 |
rs776738792 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148879 | CTTTGTGACTGGTAG[A/G]GCCTCCAACTCAAAT | 8816 |
rs776755027 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129756 | CCTCTCTGGGGCACC[A/G]GAGGTGGAGCACAGG | 8816 |
rs776757950 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111967 | CACCTGTATTAAGAC[A/G]TCAAGAAGTGGTGGG | 8816 |
rs776763435 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116128 | GATAATTGCCTAAAA[C/T]TCACCCTGTCTACAG | 8816 |
rs776764346 | snp | C/T | 3.30011e-05 | 0.00406195 | missense | DCAF5 | GRCh38.p7 | 14:69054713 | GCTTTATAAATTTTT[C/T]GCTCAACTGATTCTA | 8816 |
rs776766356 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114690 | TTTTTTTGTTTTTAT[C/T]TTTTTCTGCATAAAA | 8816 |
rs776772973 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132435 | AGCGCATCATTCTAC[A/C]AACAGTTTGAGTTAT | 8816 |
rs776788710 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065788 | GAATCTAGGGTCTCC[C/T]TTCCTCTGTCATCTA | 8816 |
rs776802374 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124862 | TGCTTCTGCTACTAT[-/A]TTTTTTTTTAATTAG | 8816 |
rs776854768 | snp | A/G | 8.68697e-05 | 0.00658994 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091015 | CACTTCAGAACTTCT[A/G]TGGTTAAGACAGAAA | 8816 |
rs776864090 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107938 | ACACGCACCTGCCCT[A/T]AAAAATTCATAGAAA | 8816 |
rs776876769 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080509 | AAAACTGAACTTCAC[C/T]TCAAGTAGTGAAATT | 8816 |
rs776886163 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101006 | AAATGTTTTCATGTA[G/T]ATCATATCATCTAAT | 8816 |
rs776899420 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100475 | AATTTTCAAAGGTCT[-/C]TGAAATTCAATCTTA | 8816 |
rs776907108 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066099 | GTCATTTCTCTGGGC[C/T]ATCTGCTTTGGTTGG | 8816 |
rs777022196 | snp | C/T | 1.73513e-05 | 0.0029454 | missense, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152948 | CCACCACTGACCTCA[C/T]GCTGCCCCCCAGGCC | 8816 |
rs777060526 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69091497 | CCTTGTATTTACCCA[C/T]TGACAGCCTTGATAA | 8816 |
rs777094880 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078340 | AACAATGAGATACCA[C/T]CTCATACCCATCAGA | 8816 |
rs777107861 | snp | C/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155083 | CATTCCAGTGGAATC[C/T]ACTTGTTCCAAGGCC | 8816 |
rs777110166 | snp | A/G | 3.32685e-05 | 0.00407837 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152805 | GTTGGAGAATTCAAT[A/G]GCATTGACACAGCCG | 8816 |
rs777124451 | in-del | -/TTTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067340 | GCCGATTTCGTATCT[-/TTTTTTTTTT]TTTTTTTTTTTTTGA | 8816 |
rs777128212 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140535 | ACTTTTAGTTAAACA[C/T]TCCTCAGGAAAAATT | 8816 |
rs777143763 | snp | C/T | 1.64743e-05 | 0.00287 | missense | DCAF5 | GRCh38.p7 | 14:69055100 | TCAGAATCGGACTCA[C/T]TGGAAAGGGCCAGGA | 8816 |
rs777145019 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151191 | TGTGGGGGAAGGAGG[C/T]TTTTGTCTGAAAGAT | 8816 |
rs777199769 | snp | C/T | 1.66175e-05 | 0.00288244 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122393 | AATCTGTGCTTAAAA[C/T]AGCTGACATCGCAAG | 8816 |
rs777284056 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063433 | CAACTCAGGACACAC[A/G]GAGAAACATGTGCAT | 8816 |
rs777289321 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064436 | AAAGAGGGGGGATGT[A/G]GGGGGATTTAAGTGA | 8816 |
rs777292791 | snp | G/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090171 | ATCAACAAAAGCAAA[G/T]AAAGAAGGAAAAAAG | 8816 |
rs777304053 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141754 | TATCAACTGGCAGAA[C/G]CCCCAGCAGAGGCAG | 8816 |
rs777330976 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055528 | GCTGATGTACTCTTC[A/G]TGGGTATAGAGGCAG | 8816 |
rs777360565 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147307 | GTATATGTTAGATGT[C/T]GAAGGTATCAATCTC | 8816 |
rs777428836 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69151215 | GAAAGATCAGGTTTC[G/T]TCAGAGGATGATCTA | 8816 |
rs777434508 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150299 | CCCAGGAAGTACTGA[C/T]GGAGATGGGCAACAC | 8816 |
rs777469348 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064951 | AGCTATCATAGAACT[A/C]AAGTGCATCAACCAA | 8816 |
rs777482733 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117362 | TGAACCTAAATAATG[A/C]GCACAGCCCAGAATG | 8816 |
rs777506385 | snp | A/T | 1.65485e-05 | 0.00287645 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119253 | AGAAAAAAGCAGACA[A/T]CTGATCATTCGTGCA | 8816 |
rs777508848 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086619 | CGTGCATGGAGTTAT[-/T]TAAAAAAAAAAAAAA | 8816 |
rs777529726 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | DCAF5 | GRCh38.p7 | 14:69054789 | AAGTGCTCCGCTCAG[C/G]GGACGAGGTTGGGGA | 8816 |
rs777557370 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099779 | AAACCCTGTCTCTAC[-/A]AAAAAAAAAATACAA | 8816 |
rs777617289 | snp | C/T | 0.000270039 | 0.0116167 | intron-variant, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091150 | CTCTCCATTTCCAGT[C/T]GTGATGCTGGCAGTA | 8816 |
rs777622871 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113015 | TTCAAGTCTTCTTTA[C/G]AGCTGACATTTTTTT | 8816 |
rs777624136 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138309 | GAATTCCTCCTCCTG[A/G]GTAATGTTCTTGGAA | 8816 |
rs777659892 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069896 | AAAGTGCTGGGATTA[C/T]AGGCATGTGCCACTG | 8816 |
rs777662443 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089329 | AATATAAATCTCTGT[A/G]TTTTATATACCTCTA | 8816 |
rs777679413 | snp | A/C | 1.70583e-05 | 0.00292042 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152937 | GGACAAGAAGCCCAC[A/C]ACTGACCTCATGCTG | 8816 |
rs777699431 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141508 | TCCCTCCCCTGTCCT[G/T]CCACCCCACAACAGG | 8816 |
rs777707378 | snp | A/T | 4.08789e-05 | 0.00452082 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075461 | TATTATAATATAGAA[A/T]AAATACAATATGTAA | 8816 |
rs777707629 | in-del | -/C | 1.64798e-05 | 0.00287047 | frameshift-variant | DCAF5 | GRCh38.p7 | 14:69054128 | CCACCACCTCCAGCT[-/C]CCCCCAAGTTCTGCC | 8816 |
rs777767572 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056586 | TCAGCCTGTAGTCAT[A/G]GCAACTCAGATGAAA | 8816 |
rs777781654 | in-del | -/AAAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086358 | CAAGACTCCGTCTAA[-/AAAC]AAACAAACAAACAAA | 8816 |
rs777786002 | snp | A/C | 0.00043592 | 0.014757 | utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153030 | CCTCCCTCGGCCTCA[A/C]GCGCGGCCGCTGCTC | 8816 |
rs777793439 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138963 | TCAGCCTGGGCAACA[C/T]GGTAAGACCCCGTCT | 8816 |
rs777818059 | snp | A/G | 1.65149e-05 | 0.00287353 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055255 | GTGGAAGGCGTTGTC[A/G]GCAGACTCATCTACT | 8816 |
rs777820513 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152499 | CCTACACTTTCAGGG[C/T]AGGCATCAGGAGAGA | 8816 |
rs777852730 | in-del | -/TCG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141459 | GCTACACCCATTAAC[-/TCG]TCATTTACATTAGGT | 8816 |
rs777874879 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073719 | TATTGCTAATTCTTT[C/T]CTATTCTCTCTATTC | 8816 |
rs777936583 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129362 | AGAGCCCTATGCAAA[A/G]GCAATCTTCAAGTAT | 8816 |
rs777995966 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69106188 | CAGCCCCCCGAGTAG[C/T]TGGAATTACAGGGGC | 8816 |
rs778019503 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084681 | CCTTCTTTTCATCTT[G/T]TATGTCCGTGAAATA | 8816 |
rs778101006 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148388 | TCATCAAGTATAAGC[G/T]AGTCTTTATAAAAAG | 8816 |
rs778103024 | snp | C/G | 1.66142e-05 | 0.00288216 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116540 | CTCCAGGTACCTGTG[C/G]GCCACTGGCAGGCAG | 8816 |
rs778103858 | in-del | -/ACATCT | 1.65441e-05 | 0.00287607 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119249 | AAAAGAAAAAAGCAG[-/ACATCT]ACATCTGATCATTCG | 8816 |
rs778105857 | snp | C/T | 3.30115e-05 | 0.00406259 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055180 | GGCTGCATCCTCACA[C/T]GTGGGTGTTGGTGGA | 8816 |
rs778154159 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072734 | AAGACATGCTAAAAA[A/T]AATCTTAAAAGATAC | 8816 |
rs778192756 | snp | A/T | 1.66846e-05 | 0.00288826 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116339 | GGCAGAGGAAAGTTT[A/T]AACACCTATGAATAA | 8816 |
rs778208374 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093207 | ATGTTGGGTTAATTT[C/T]TGGAGCACTGAATTA | 8816 |
rs778217715 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69089158 | CAGTTAGAGAAGACT[C/T]AGGCCCACAAAGCTA | 8816 |
rs778218310 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099980 | TCAAAAGGAAAATTA[C/T]TTAAGCTTTAAAAGG | 8816 |
rs778229428 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067066 | TAACCTTTTAAACAT[-/A]CTACATAATTTACTA | 8816 |
rs778241419 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051219 | AGGAAAAAAACATAA[C/G]AGGCACTTCCAAATA | 8816 |
rs778242016 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072364 | ACTTTGATAAAAAGA[A/C]GTACTTAATTACAAA | 8816 |
rs778242051 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075735 | GTGATCCGCTGGCCT[C/T]GGCCTCCCAAAGTGC | 8816 |
rs778297165 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135121 | TCGAAGTGTGTCCCA[C/T]GGACCCCAGAAGGTC | 8816 |
rs778390104 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120844 | CTTGAGAACAGTCCA[A/G]CTGGACAAACAACTA | 8816 |
rs778401855 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111625 | CAGGGGAAACTTTTG[C/T]TTTTCCTGAATTCTC | 8816 |
rs778415703 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104751 | AATCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA | 8816 |
rs778457257 | snp | C/G | 6.63482e-05 | 0.00575931 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118292 | TGCTGGGAGATAAGA[C/G]AGCAAGACAGAGGCA | 8816 |
rs778461856 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054547 | CTGGGCCATTGCTAT[A/G]TTTAGACAGGCTTCC | 8816 |
rs778481326 | snp | C/G | 1.65187e-05 | 0.00287386 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054667 | TTTGTTATTTGAGTA[C/G]GAGATATAAGAGTAG | 8816 |
rs778489813 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124467 | GCTCCTAGAAAGAAA[C/T]TGTCTTTGCTACTTG | 8816 |
rs778499081 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075930 | GTTAGCTAAAACTCA[G/T]CAACGACAACAAAAA | 8816 |
rs778508339 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087886 | ACATGAGAAAAAACA[C/T]CTTGCTGAATGAAGC | 8816 |
rs778516084 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066630 | ACTTACTACCGTAGG[A/G]GACCCCAGGATCCCA | 8816 |
rs778516716 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114117 | AGACACATGCAATCT[C/T]ATACACAGTTGGCAG | 8816 |
rs778573331 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130627 | AAAGTTTACTACTTA[C/T]ATATGTACAATGCAG | 8816 |
rs778586170 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | DCAF5 | GRCh38.p7 | 14:69054776 | ATCTCTAGCGTGGAA[C/G]TGCTCCGCTCAGGGG | 8816 |
rs778600582 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125652 | AAGAAAACCTATATA[C/T]AACATAAATATCTAA | 8816 |
rs778693118 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072049 | ACAAGGCACAGCTGG[A/G]GGTGTCATTAAACAA | 8816 |
rs778695588 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115639 | CTCCCCCATGGGACT[G/T]AAGGAACATAAAAGA | 8816 |
rs778712277 | snp | A/C | | | | | GRCh38.p7 | 14:69053504 | AAGGAAGGTCTTATG[A/C]GACAATAAGCGCACA | 8816 |
rs778767360 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075313 | CAACAGAGCCAGCAA[C/T]AGCAGTACATTCATG | 8816 |
rs778768908 | snp | C/G | 1.67494e-05 | 0.00289386 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152904 | AGTGAGCAGGGGGTC[C/G]CCATGCAAGCCCCGC | 8816 |
rs778789696 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103618 | TCAGCTATACATGCA[C/T]TCATTTGTGTTAGGT | 8816 |
rs778802470 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056851 | AAGAGGCTGAAGAAA[A/C]CTTCTAGATTAGCAT | 8816 |
rs778816415 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088167 | CCTAGCCCAATCCAC[C/T]TATTTTTGCTGCCTG | 8816 |
rs778877316 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116869 | GGTAGGGTTATTATG[A/C]TTTTAATCCAATTGT | 8816 |
rs778885010 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081623 | AACAACTCTCTCTCA[A/G]TAGATTTCAGGAAGG | 8816 |
rs778892189 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070195 | AGCAACTCAACCTGT[A/G]AAAACCCTAAAGCCC | 8816 |
rs778909282 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068332 | TGAAGTTAAAGTTAT[C/T]TGCTAAAATGAGGTT | 8816 |
rs778921430 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148102 | TGTTCATTTTCTTCG[-/CA]AAAAAAAAAAAAAAA | 8816 |
rs778952476 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137283 | CAGTAAGGAAAGTTA[C/T]TAAGTTAGTGGATGA | 8816 |
rs778977897 | in-del | -/GCTGGGAGGGT | 1.67036e-05 | 0.0028899 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152717 | GAGCGAGAGGGGGAG[-/GCTGGGAGGGT]GCGGGGAGGCGCGGG | 8816 |
rs779000548 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109662 | TTTGTTGTTTATTTA[C/T]GTTTGTGTAATATTC | 8816 |
rs779032272 | snp | A/T | 3.30267e-05 | 0.00406353 | missense | DCAF5 | GRCh38.p7 | 14:69054047 | CCGCAACAATCTTTG[A/T]GTAGGAGTGTCCCTG | 8816 |
rs779119029 | snp | G/T | 1.7849e-05 | 0.00298734 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091854 | ACTCATGGCACTTTG[G/T]AGGGACAGGTTTCCA | 8816 |
rs779120091 | snp | C/T | 3.29968e-05 | 0.00406169 | missense | DCAF5 | GRCh38.p7 | 14:69055151 | CGCAGAGCAGACAGA[C/T]GCTGCTGGCGAGAGG | 8816 |
rs779124260 | snp | C/T | 1.65548e-05 | 0.002877 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69053989 | GGTGTCAGTGGGGTC[C/T]TCTCTTGTTCCAGCA | 8816 |
rs779150946 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120628 | CACAACCAACAGTCA[C/T]TTAAATAGAAAGCAA | 8816 |
rs779175899 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090691 | GCCAGTTTCTCAAAG[A/G]AATTTTTCTTTTATG | 8816 |
rs779184352 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097273 | ACTGCTGACTGATGA[A/G]ACACGATTACAGGAA | 8816 |
rs779210816 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113014 | ATTCAAGTCTTCTTT[A/G]GAGCTGACATTTTTT | 8816 |
rs779212305 | snp | A/G | 9.88386e-05 | 0.00702919 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055042 | GGGTGACCGTGGCCG[A/G]GGAAAGAGATCTGTG | 8816 |
rs779248278 | snp | C/T | 1.65053e-05 | 0.0028727 | missense | DCAF5 | GRCh38.p7 | 14:69054444 | CATGGCTGCTGTGCT[C/T]ATGGCCTGGGCCATT | 8816 |
rs779334159 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062364 | TTTCTCTAAAAGGAC[A/G]GAAGGGGAAGGTGCC | 8816 |
rs779345250 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107362 | TAACCACTGCTTCCA[C/T]CTTGTAAGACCAACA | 8816 |
rs779347146 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121616 | TTGGTTTTAGATCTA[C/T]TGTATTTAAGTTGCT | 8816 |
rs779359844 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112764 | ATACTCCGATGGCAC[A/G]TAATGCTTAATAAAT | 8816 |
rs779364959 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103084 | ATACATGTGGGTCCA[C/T]TATTGACTGAAACAT | 8816 |
rs779370581 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084457 | AACACGTAGACAGAC[A/G]ATGCTCTTTTCTGCC | 8816 |
rs779395732 | snp | A/G | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153456 | CACTCCGCGGAGTTG[A/G]ATGCGCGTAACAATC | 8816 |
rs779460533 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063295 | AACTTGTAACATAGA[C/T]AAACATGTTATCATT | 8816 |
rs779492836 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053117 | CATGTTGCAGCACTG[C/T]TCAATTTGCAAACAG | 8816 |
rs779495461 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128955 | AGACTTTGTCTCTAC[C/T]AAAAGAAAAAAAAAG | 8816 |
rs779522278 | snp | A/T | 1.65105e-05 | 0.00287315 | missense | DCAF5 | GRCh38.p7 | 14:69054317 | GGAGAAGGCGGCTCC[A/T]CAGCCCGACTGCTCA | 8816 |
rs779524611 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132517 | TCACCCCATCCAGCC[C/T]AAAAGAGTTTTCTGT | 8816 |
rs779535044 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123137 | CATCCATACAAGGGC[A/G]TACTATGAAGCCATT | 8816 |
rs779579856 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075265 | CCTCTACTGCTAAAG[A/T]TCTGTCCCCTCAGGG | 8816 |
rs779580722 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066441 | CACCTGGCCAGCTGA[C/T]ACTCCTTTTTAAGTT | 8816 |
rs779586512 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051960 | ATTTACAATTATCTG[C/T]GAATAGTCAAAGACA | 8816 |
rs779622970 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137179 | GCAATTTTCCATAGT[A/G]AAGTATGGAATTAGT | 8816 |
rs779638960 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101643 | CAGGAATATGTTCTA[C/T]GAAATGTGTTGTTAG | 8816 |
rs779640667 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087012 | CTATTAGACCAGGCA[C/T]CATATGAGACTAAAG | 8816 |
rs779656125 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080239 | TGCTGAAAGGATCAT[A/C]CCCTCCTGGACTCAG | 8816 |
rs779690483 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69125099 | ACAATAAAGTCATTG[A/C]GCTAAGATTCAAAAG | 8816 |
rs779695541 | in-del | -/A | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089737 | CACAGGTTCTCAACC[-/A]GGGGCAATTTTCCCC | 8816 |
rs779702114 | snp | C/G | 1.65173e-05 | 0.00287374 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054637 | CTCCCCGGTCACCAA[C/G]GAGGTCTCTCCATCT | 8816 |
rs779706860 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137957 | AGTATACATAGGGTT[C/T]AGTACCATCTGCAGT | 8816 |
rs779789894 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054571 | GGCTTCCTTACTGGA[A/G]GAAGGGGCTGGGTTG | 8816 |
rs779830586 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127757 | GGAATAAGGGGTACA[A/T]GGAAAACCTCTGTAC | 8816 |
rs779838964 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074204 | ACGTTTTGTGTAATA[C/T]ACTTGGCATAGTCCT | 8816 |
rs779870131 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062432 | CATGTAGGTGTGGGG[A/G]TTAAATCGGACTTGG | 8816 |
rs779913970 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114368 | AAATTGAATGCCATA[C/T]AGTCATTAAAAGAAG | 8816 |
rs779928846 | in-del | -/AGAGCTGCT | 1.64734e-05 | 0.00286992 | cds-indel | DCAF5 | GRCh38.p7 | 14:69054981 | CTCCTCCTCATCCTC[-/AGAGCTGCT]AGAGCTGCTAGAGCT | 8816 |
rs779950939 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060752 | GGCCAGGCTGGTCTC[A/G]AACACCTAACCTCAG | 8816 |
rs779993672 | snp | C/T | 4.94181e-05 | 0.00497057 | missense | DCAF5 | GRCh38.p7 | 14:69054917 | CGGGTTGTCTTCTGT[C/T]GGCGCCGCATGGCAT | 8816 |
rs780003053 | snp | A/G | 4.96397e-05 | 0.0049817 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69053956 | GCCATGAACAGCCCT[A/G]CTACTATCTGTGGCT | 8816 |
rs780011257 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115464 | CCCGTGAAATAAATT[A/G]TAACATCACTTAGTT | 8816 |
rs780026579 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129199 | TGATGACAGCCCAAT[A/C]CATGGGAGATTGGAA | 8816 |
rs780027890 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081498 | TGATCTGAATGTTTA[C/G]TGATCTAGACATTTT | 8816 |
rs780030541 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083291 | TTAGAGTTTCAAAAA[A/G]GTCCAGGATTCAAAA | 8816 |
rs780035364 | in-del | -/C | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153417 | GGCGCCGGGCGGAGA[-/C]CCCCTCTGCACCCCA | 8816 |
rs780070386 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148691 | CAGAGCAAGACTCCA[C/T]TGCCCCCACCGCCCA | 8816 |
rs780133596 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080998 | TAAAAACTCACTTCA[C/T]GTTCTGCTTTAGTAC | 8816 |
rs780138854 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097109 | AGAGGAATGCTGAAG[A/T]GGAAAGAAGAAAAGT | 8816 |
rs780193032 | snp | A/T | 3.295e-05 | 0.00405881 | missense | DCAF5 | GRCh38.p7 | 14:69055032 | CTTCGGGGCTGGGTG[A/T]CCGTGGCCGGGGAAA | 8816 |
rs780294447 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105235 | AGAAGATGGGACAAT[C/G]CAAACGGCTATCATT | 8816 |
rs780297054 | snp | C/T | 4.95544e-05 | 0.00497742 | missense | DCAF5 | GRCh38.p7 | 14:69054396 | CGCTATTGCCAGTGT[C/T]CTGAGAGGTACCCTC | 8816 |
rs780367161 | snp | C/T | 1.66941e-05 | 0.00288908 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091828 | TGGGTCCCGTTGCTG[C/T]TGAATCGTACACTCA | 8816 |
rs780384727 | snp | C/T | 0.000115507 | 0.00759869 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054310 | GACAGGAGGAGAAGG[C/T]GGCTCCTCAGCCCGA | 8816 |
rs780386027 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145792 | TTTCATTCCACCCTT[A/G]AGTATCTAAATTCAG | 8816 |
rs780415240 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061552 | CAATGTGCAAATGAT[A/C]CAAGTATTTAGTATT | 8816 |
rs780420965 | in-del | -/AAAAAATTCCAATTTAATACATTTTGGA | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051879 | TGTATATAAAGGATT[-/AAAAAATTCCAATTTAATACATTTTGGA]AAAGCAAATGTAAAA | 8816 |
rs780449551 | snp | C/T | 1.65225e-05 | 0.00287419 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69119220 | ATGGAGGATAACTTG[C/T]TCATCATTGCCTGCA | 8816 |
rs780472961 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054184 | AGGGTGTAAGCGTCC[A/G]TTGTTGTGGTTGGCA | 8816 |
rs780482483 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124072 | AAGTCAAATCACACA[A/G]TATTTCTCCTTCTAG | 8816 |
rs780483479 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118551 | AGTTTTGTATTTTCA[C/T]TTATTACAGAATGCA | 8816 |
rs780542023 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097926 | CTTCCTAGCTTGTCT[C/T]TGCTTTCATTTTTGG | 8816 |
rs780604410 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075766 | TGGGATTACAGGTGT[A/G]AGTCACCACAACTGG | 8816 |
rs780605662 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111530 | CTGACAGAAAATAAA[C/G]AGATTGGAAGGGAGA | 8816 |
rs780630450 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065342 | CCTCATGATCCACCC[A/G]CCTCGGCCTCCCAAA | 8816 |
rs780633824 | snp | C/T | 1.64985e-05 | 0.0028721 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055294 | CGGGGAGCGAGGCAA[C/T]GAGGCCGAAGACTCT | 8816 |
rs780657467 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131026 | ATATATTAGGTGCAC[A/C]CAGCTCTCAAATTGT | 8816 |
rs780682375 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086065 | CTGGGAGCATTAAAA[C/T]ATAATAGTGGGCTGG | 8816 |
rs780708914 | snp | C/G | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051561 | CTAAAAATGATCTTT[C/G]TTGGCTTCTCAAGTT | 8816 |
rs780752254 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147646 | TGGTCAGAGACCCAT[G/T]TGAACTAGAAATAGG | 8816 |
rs780758043 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69148452 | CTGTAATCCCAGGAC[A/T]TTGGGAGGCTGAGGT | 8816 |
rs780776484 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115400 | ACCTAGGAGTAAAAA[C/T]CATCAAGGAAGATAA | 8816 |
rs780786528 | snp | G/T | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090521 | TCAGAAAACTTAAAA[G/T]AACATTCTCATCTAT | 8816 |
rs780813160 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064198 | TAAAGAACCCAAAAA[C/T]AGTTGTCTTGACAGA | 8816 |
rs780823126 | in-del | -/GCGGGGAGGC | 3.96999e-05 | 0.00445515 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152728 | GGAGGCTGGGAGGGT[-/GCGGGGAGGC]GCGGGGAGGGGAAGG | 8816 |
rs780832932 | snp | A/T | 1.65015e-05 | 0.00287237 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054466 | TGGGCCATTGCTGGG[A/T]GTTCTAGGAGTCTCT | 8816 |
rs780833301 | snp | G/T | 1.66626e-05 | 0.00288635 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062560 | TGAAATGAATGAAAG[G/T]AAATAGGTTCCAGTA | 8816 |
rs780861507 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69114215 | ACATGCATCCTTTGA[C/T]GTAGCAAAGTCCGTA | 8816 |
rs780874716 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107178 | TGTTTGCAGAGCTCC[C/T]CTCCATTTACCAGGC | 8816 |
rs780890835 | in-del | -/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053803 | TATTCACTAAACAAT[-/T]TTTTTTTTTTTGTAA | 8816 |
rs780895583 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093480 | AAAAAAGAGCTATAT[-/A]ATTACCAGAAGAGAG | 8816 |
rs780925141 | snp | G/T | 1.64795e-05 | 0.00287045 | missense | DCAF5 | GRCh38.p7 | 14:69062419 | CAGAAGAGCAGATCA[G/T]GTAGGTGTGGGGATT | 8816 |
rs780953402 | snp | A/T | | | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154254 | GTGGTAATAAGCTAC[A/T]GAAATAGGCACTTGT | 8816 |
rs781055780 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100172 | TACATTAACTAGACT[A/G]TAGAACTTGGGTCAT | 8816 |
rs781067009 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089472 | AAAGAAGTCTTGTCT[A/G]TCAGAGAGAATAAAA | 8816 |
rs781070270 | in-del | -/AAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086372 | AAAAACAAACAAACA[-/AAC]AACGACAACAAAAAA | 8816 |
rs781091967 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078814 | GAAGAAGAAGTTCTA[C/G]AGATGGATAGTGGTG | 8816 |
rs781092744 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058024 | TCTTTCATTTGGCAA[C/T]TGAATGCCTCAACCA | 8816 |
rs781125862 | snp | A/C | 0.000260044 | 0.0113998 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091181 | AAAAGAAAAAGAGTC[A/C]GCATCTGGCTCCCTC | 8816 |
rs781142619 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | DCAF5 | GRCh38.p7 | 14:69054909 | TGTCTTCTCGGGTTG[C/T]CTTCTGTCGGCGCCG | 8816 |
rs781142918 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127490 | AGGGTTTGGAGGCAG[C/G]GGTTGAATATATGGA | 8816 |
rs781174102 | in-del | -/A | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089303 | CCCTAAGGAGTCAAC[-/A]AAAAAAGCCAAATAT | 8816 |
rs781230522 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69132263 | TATTCTCACCAACAA[C/T]GTACAAGAGTTCCAA | 8816 |
rs781234978 | snp | C/T | 1.64909e-05 | 0.00287144 | missense | DCAF5 | GRCh38.p7 | 14:69054281 | CTGTTGAGAGTGGAG[C/T]CAGATGCCTTGGGGA | 8816 |
rs781239132 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091760 | GAAACACAGGCAGGC[A/G]GGAATGGATGTCATA | 8816 |
rs781269931 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096148 | AGTCACAGTCCACAC[G/T]GGTCGCATTCAAGTA | 8816 |
rs781432404 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117156 | AATACAAAGAAAGCA[C/T]TTCTCAGTCTATGAC | 8816 |
rs781541138 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137082 | TTCCTATAATTAATA[C/T]ATAATAGTTGTTTAA | 8816 |
rs781554529 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066794 | AACATTCAGCCAGGG[A/G]TTTATTGCCTCAGGC | 8816 |
rs781554854 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086227 | ACCGGGCGTGGTGGC[A/G]CGTGCCTATAATTCC | 8816 |
rs781610832 | snp | C/T | 1.65225e-05 | 0.00287419 | missense | DCAF5 | GRCh38.p7 | 14:69055215 | AGGCTACTGTGTTTG[C/T]GGTGGTGACCCGCAG | 8816 |
rs781622070 | snp | C/T | 1.65179e-05 | 0.00287379 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69118265 | CATGAGCAAACACGT[C/T]CAATGTCTCACTGCT | 8816 |
rs781653743 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69101065 | TGTGGTTAACATCAA[C/T]CTATGTTACACTGGA | 8816 |
rs781705088 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122859 | TAACTAAGAAATCAC[C/G]TGACTCTTACAGTAA | 8816 |
rs781716257 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086896 | TTCAAAAGACCAGTA[C/T]AAGAGATCTCAGTGC | 8816 |
rs781768320 | in-del | -/TTTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122702 | TCATGGAAGTCCTTT[-/TTTG]TTTGTTTGTTTGTTT | 8816 |
rs796094645 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69080261 | TGGACTCAGGCTGGT[C/T]GGGGCCACTGAGTGG | 8816 |
rs796100631 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69088146 | CACCACTCCTTAATG[G/T]TTACTCCTAGCCCAA | 8816 |
rs796107795 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69115125 | GAGAACACTGCAGAT[A/G]AACACAGTTGTCTTC | 8816 |
rs796131084 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110228 | ATGTATGTATTATGC[-/T]TTTTTTTTTTCTGAT | 8816 |
rs796131450 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69062088 | TTTATTTTTATTTTT[A/T]ATTTTATTTTTTAAG | 8816 |
rs796196981 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135145 | AAGGTCTGCAAAGTC[-/A]AAAATTTTTTTCGCA | 8816 |
rs796201825 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138130 | TCAAGACACCTATTT[-/A]AAAAAAAAAAAGGAA | 8816 |
rs796239962 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69144575 | AGCGAGACTCCGTTT[-/A]AAAAAAAAAAGATTA | 8816 |
rs796254666 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152206 | GGCGGCCCACAGCGA[C/T]CCTACCGCCCCAGTC | 8816 |
rs796254951 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094047 | ACTCAAAAACAATGA[A/G]AGGCTTTCAATCCAA | 8816 |
rs796260818 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118073 | GAGGTAATAAATTGG[A/G]TCTTCAATGAATCTG | 8816 |
rs796282764 | in-del | -/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053814 | CAATTTTTTTTTTTT[-/T]GTAAGGCTACTTTTG | 8816 |
rs796344071 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078698 | TCCTACTAGAGTAGT[C/G]ATGAAAATTCAGACA | 8816 |
rs796345683 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123996 | AATCACTGTGCCCGG[C/T]CAAGTAGTCACTATT | 8816 |
rs796389336 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140910 | TCACCCCCGCCTAGG[G/T]ACTGAACTCTGTCAG | 8816 |
rs796409867 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69059486 | TAGGAGTTAGGCACA[C/G]GTAATTCACAAGGCA | 8816 |
rs796438990 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69104577 | GAAGTGAGAGATGGC[C/T]GGGTGGGGTGGCTCA | 8816 |
rs796478309 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086349 | GGTGATAGAGCAAGA[C/T]TCCGTCTAAAAACAA | 8816 |
rs796479560 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69120177 | CAGTCTTGACCTCCT[A/G]TGCTCAAGCAATCTT | 8816 |
rs796508945 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097590 | TATTATTATTTTTTT[A/T]TTTTTTTTTTTTTTG | 8816 |
rs796565037 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133792 | AAACATGTTAAAAGT[A/G]AGGTCCTGGCTTGCC | 8816 |
rs796633068 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103865 | TGGAATTATGCAGCA[C/T]GTATTCTTTTGAGAT | 8816 |
rs796652529 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69074408 | CTAAGAAAAAGAAAA[-/G]GGGGGGGAAACTAAG | 8816 |
rs796652854 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082939 | GACTCTTAGCCAGGA[A/G]CCATGCATTAAAGAA | 8816 |
rs796713511 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69094438 | CTTCTGGGCAGGGAA[C/T]TCTGACCTCTCACAC | 8816 |
rs796722603 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082836 | CAAAGCTCTTCTACT[A/G]AAAGTAAAATTTCTA | 8816 |
rs796745257 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095551 | TTTGTTTTTTTAAGT[-/AC]ACACACACACACAAA | 8816 |
rs796780384 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079651 | GTGAGGTCATTCCTT[C/T]ATTCATTAAACAAAT | 8816 |
rs796796576 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69145674 | ATAAGAATATTTTTT[-/T]AAACAATGTGAGGCA | 8816 |
rs796856914 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069459 | TTAAAAAGGGAGAAG[C/G]CCTTCTTTTTCTTCT | 8816 |
rs796891700 | in-del | -/TTTTTTTTTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067352 | CTTTTTTTTTTTTTT[-/TTTTTTTTTT]GAGACAGGGTCTCAC | 8816 |
rs796914984 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123063 | GCAAACCATAGCAAG[C/T]TCTACACCTCCACCT | 8816 |
rs796919373 | in-del | -/AAG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69087367 | GTAGGAAGTGAAAGC[-/AAG]AAGAACCTTTGGGCT | 8816 |
rs796922032 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072645 | AAAAAAAAAAAAAAA[-/A]CGAGAGAAAAGAAAA | 8816 |
rs796966733 | snp | A/T | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089676 | TCTGCCTATGACAAT[A/T]CCTGCCCCAATGCAT | 8816 |
rs796974837 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142049 | TCTGTAATCCCAGCA[C/T]CTTGGAAGGCCAAGG | 8816 |
rs796983764 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69109436 | TACAACCATGAAATT[G/T]CCACCCAGATCAAGA | 8816 |
rs796983844 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086638 | AAAAAAAAAAAAAAA[-/A]GCAAAGTTATAACTT | 8816 |
rs796989489 | in-del | -/AT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102620 | CACACACACACACAC[-/AT]ATTAGCCTAGACCTA | 8816 |
rs796996668 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69064472 | CCCAAGTCATAAAGC[C/T]AGAAAATGGCAGAGC | 8816 |