SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2572 | snp | A/G | 0.164219 | 0.234823 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959582 | GAATAAACATCTCAC[A/G]AACTGTCGCTCCTAG | 26094 |
rs741227 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942063 | GAGAGAGGATGGGGA[C/T]GTAGGCAGAGATGTC | 26094 |
rs887936 | snp | A/G | 0.361894 | 0.223562 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939960 | TTCCAAGCCAGGAAC[A/G]GGTCTCAGCCTTCCC | 26094 |
rs1076458 | snp | A/G | 0.469049 | 0.120489 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927170 | GTGGGCTCCCCGGGG[A/G]CTTCAGAAACCATGA | 26094 |
rs1079560 | snp | G/T | 0.107341 | 0.205301 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926849 | GCCTTCAGCAGCAGG[G/T]CTCAGAGAAGCGCTT | 26094 |
rs1110058 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957584 | AACAGGTGAAAAATC[C/G]ACTTAAAAAGGAGGC | 26094 |
rs2098321 | snp | A/G | 0.37778 | 0.214877 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927414 | CAGTGAGTCGAGATC[A/G]TGCCACTGCACTCCA | 26094 |
rs2098322 | snp | C/T | 0.494143 | 0.0537956 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926576 | CAGCCCTCGAATCGA[C/T]GCCAGTAGGCACCCC | 26094 |
rs2240980 | snp | C/G | 0.449718 | 0.150375 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942975 | TCAGCATCCATGCCC[C/G]CACCCTCTGTTTCTG | 26094 |
rs2240981 | snp | C/T | 0.375 | 0.216506 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943490 | TGGCTAAACCTGCAG[C/T]CCAGTGTGCCTTTGG | 26094 |
rs2243443 | snp | C/G | 0.330249 | 0.23677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947257 | TGGACCTGGGTATCT[C/G]TGGGCTTCATGACAT | 26094 |
rs2243596 | snp | A/G | 0.498774 | 0.02473 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961952 | CCCCAGCTCTCCGTC[A/G]GAGCACGTCTGTCTT | 26094 |
rs2246976 | snp | C/T | 0.392186 | 0.20897 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946031 | ACCAACCGGAAGGTA[C/T]GTTGCCCATCCCTGT | 26094 |
rs2247080 | snp | A/C | 0.375399 | 0.216275 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945756 | TCTCCACTCTCGCTC[A/C]TGGAGAGGAACTCTC | 26094 |
rs2286833 | snp | A/G | 0.0454566 | 0.143743 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947122 | ATAACTTTCCATCTC[A/G]CTGTGTGCTTCCTCA | 26094 |
rs2286834 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952136 | GCTCAGAACAGATTC[A/G]GACGCCCGTGCACAT | 26094 |
rs2302586 | snp | C/G | 0.371791 | 0.218327 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938117 | CCCAGTGTGCTTCTG[C/G]CATTGTACACATGGC | 26094 |
rs2302587 | snp | C/T | 0.393594 | 0.204648 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938087 | GCAAAAGTGGCTCCC[C/T]AGAGCGGCACACTTG | 26094 |
rs2302588 | snp | C/G | 0.167495 | 0.236042 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938044 | ATCACGGAGTCTGAA[C/G]CAAGGGTTCTGCTGG | 26094 |
rs2333012 | snp | A/G | 0.336702 | 0.234484 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942905 | CGAGGAGAGATGGGC[A/G]TCAGCGGGGCAGGGA | 26094 |
rs2535908 | snp | C/G/T | 0.00157319 | 0.0280047 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958724 | GCCCCCCAGCCGCGA[C/G/T]GAGAAGGCCACACTG | 26094 |
rs2535909 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955258 | CCCCTGCACTGTCCC[C/G]TTTGGCCTTTCTCTC | 26094 |
rs2535910 | snp | C/T | 0.32955 | 0.237006 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953934 | GTCGTGTTTACAGTA[C/T]GAATAGTACTGATAT | 26094 |
rs2535912 | snp | A/G | 0.330249 | 0.23677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951492 | TCCTGAGTAGCTGGG[A/G]TTACAGGCATGTGCC | 26094 |
rs2535913 | snp | C/T | 0.330249 | 0.23677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948525 | CTTGGCCTCTTTAGC[C/T]CTCTGGTTAGATCAT | 26094 |
rs2535914 | snp | A/G | 0.330249 | 0.23677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943913 | GGGCCCTGCTGTGGC[A/G]GTCTCCTGGGGCAGG | 26094 |
rs2806031 | snp | C/T | 0.227074 | 0.248947 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961868 | GCATTGTAGTGGCCA[C/T]CTGCTGGAGAGGATG | 26094 |
rs2806032 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958247 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 26094 |
rs2806033 | snp | A/G | 0.49607 | 0.0441545 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958106 | TTTTTTTTTGAGATA[A/G]GGTCTTGCTGTGTTG | 26094 |
rs2806034 | snp | A/C | 0.388709 | 0.208002 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955642 | TTGGAGGATCCGCAC[A/C]GAGGTCACTGCTGAA | 26094 |
rs2806035 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953764 | AAATAAATAAATAAA[C/T]tatatatatatatat | 26094 |
rs2806036 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953734 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 26094 |
rs2806037 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952719 | caataagagcaaaac[A/T]ccgtctcaaaaaaaa | 26094 |
rs2806038 | snp | C/T | 0.331874 | 0.236213 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951155 | TGTCTCTACAAAAAA[C/T]ACAAAAACTAGCTGG | 26094 |
rs2806039 | snp | A/G | 0.377187 | 0.215229 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949109 | CATACCGCTCTGGGT[A/G]GTAAGCTCCAAATTA | 26094 |
rs2806040 | snp | A/G | 0.330016 | 0.236849 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948357 | CTATGACCCTTTGAA[A/G]TGTAAGCTGGGTGTG | 26094 |
rs2806041 | snp | A/C | 0.371987 | 0.218218 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948187 | AAAAAAATTAAAATC[A/C]AAAAAAACTCCTTTG | 26094 |
rs2806042 | snp | C/T | 0.499982 | 0.00299515 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947939 | ATTAACATGTGGTTT[C/T]GGGTGAGTCAAGTCT | 26094 |
rs2806043 | snp | C/T | 0.376791 | 0.215463 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947613 | TGTGCTGCTCCTTTC[C/T]GCCTTGTTCCTCTGC | 26094 |
rs2806044 | snp | C/T | 0.463881 | 0.12944 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947608 | TGCTCCTTTCTGCCT[C/T]GTTCCTCTGCTACCA | 26094 |
rs2806045 | snp | A/G | 0.46865 | 0.121211 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944816 | caggtgtgagccacc[A/G]cacctggccCTAttt | 26094 |
rs2907953 | snp | C/T | 0.432797 | 0.170544 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962412 | CTCAAGCAATCCTCC[C/T]GTCTCGGCATCACTT | 26094 |
rs2998006 | snp | A/G | 0.493386 | 0.0571263 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962406 | CAATCCTCCTGTCTC[A/G]GCATCACTTCGGCCT | 26094 |
rs3061066 | in-del | -/AC/ACACGCAC/ACGCAC | 0 | 0 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962511 | CACACACACACACAC[-/AC/ACACGCAC/ACGCAC]GCATGCACACTCTCT | 26094 |
rs3213729 | snp | C/G | 0.320814 | 0.239761 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926538 | ACAGTCTTACCTGTT[C/G]AGCGTGTCCCTTCCG | 26094 |
rs3214336 | in-del | -/T | 0.376989 | 0.215346 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952025 | TACCAGAAGCATGTG[-/T]TTTTTTTACAGCATC | 26094 |
rs3742832 | snp | C/T | 0.444267 | 0.157354 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941647 | ATGTAATGAAGGAAA[C/T]AGGCACTAAATTGGC | 26094 |
rs3815460 | snp | C/G | 0.164445 | 0.234905 | missense | DCAF4 | GRCh38.p7 | 14:72955551 | TTAATGGCTGCCGCT[C/G]TGGGGAAATCTTTGC | 26094 |
rs3815500 | snp | G/T | 0.376876 | 0.215412 | utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72937972 | TTTATTCATTTCTGT[G/T]CCTAAAAGAGAAAAA | 26094 |
rs3832967 | in-del | -/A | 0.330249 | 0.23677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941661 | TTTAGTTCCATAGGA[-/A]TGTAATGAAGGAAAC | 26094 |
rs3832968 | in-del | -/A | 0.364609 | 0.222182 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941611 | TTATATGCATAAAAA[-/A]TCTGACGGTGTCCTT | 26094 |
rs3965998 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927640 | acaggcgtgagccac[C/T]gcgcccggccTGAGG | 26094 |
rs4395014 | snp | C/T | 0.367708 | 0.220556 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945531 | TTTTTCCTATTGCGC[C/T]ACAGCCTTCGTGATG | 26094 |
rs4903078 | snp | A/G | 0.363359 | 0.222822 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937730 | GGCCGACCTGGCAAC[A/G]TTTCTGTGGGGTAGG | 26094 |
rs4903079 | snp | A/G | 0.372391 | 0.217992 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941186 | GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 26094 |
rs4903080 | snp | A/G | 0.410061 | 0.192043 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949416 | AGCTGTGATCACACT[A/G]CTGCACTCCAGCCTG | 26094 |
rs4903081 | snp | C/T | 0.409721 | 0.192325 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959718 | TGGGACCAGCTTTCA[C/T]AGCCTTCCTGGAGAG | 26094 |
rs6574112 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929739 | GCCCATTTCTCCTTG[A/G]AGACCTTCAGTGACT | 26094 |
rs7141910 | snp | C/T | 0.478354 | 0.101757 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952972 | tgctgggattacagg[C/T]gtgagccacaatgcc | 26094 |
rs7141933 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953022 | tttttttttttgaga[A/T]ggagtttcactcttg | 26094 |
rs7142086 | snp | C/T | 0.281049 | 0.248064 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924885 | CCTGTCACTTCCCAA[C/T]TCTAGAACCCTCAGA | 26094 |
rs7142161 | snp | A/G | 0.121369 | 0.214369 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940686 | ACCTCCACCTCCCAG[A/G]TTCAAGCAATTCTCC | 26094 |
rs7142775 | snp | G/T | 0.160938 | 0.233598 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955191 | CCCTTAAAAGTGAAT[G/T]AACCCACTAACCTGC | 26094 |
rs7143528 | snp | C/T | 0.44755 | 0.153212 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934132 | CTGCAGGCCCCCCGC[C/T]CCCACTGCCTTACGT | 26094 |
rs7143683 | snp | C/T | 0.409721 | 0.192325 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958345 | TTGAACGTTCCGTGA[C/T]ATCAAGAGCAGCAGA | 26094 |
rs7144128 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928329 | ctcccgagtagctga[A/G]actacgggcgcacgc | 26094 |
rs7144193 | snp | C/T | 0.390745 | 0.206618 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958607 | GTGTCTCTCCTCTTT[C/T]CTAGTGGGCCAGGAC | 26094 |
rs7144310 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928438 | ccgacctcgtgatcc[G/T]cccgcctcggcctcc | 26094 |
rs7144738 | snp | A/C | 0.372391 | 0.217992 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958973 | TGGAGATGCTCAGGA[A/C]AGTTATTTGAGTTAA | 26094 |
rs7145222 | snp | A/C | 0.323434 | 0.238972 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929079 | TGCGGGCGGCACGGA[A/C]GCCCGGGGCTGCTCC | 26094 |
rs7149675 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929295 | GTGTGGAAAACTGCT[A/G]GACTGTGAGAGAGAG | 26094 |
rs7150054 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929423 | TCTCAGATTTGCTgc[C/T]gcgcgtggtggctca | 26094 |
rs7154677 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942626 | CCTGGGGCTCTTCCC[A/G]GCAGCCGTATCCTGG | 26094 |
rs7155130 | snp | A/G | 0.446902 | 0.154045 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935643 | GCCTGTATGAGTTAG[A/G]GGTGAACACATGCTC | 26094 |
rs7155812 | snp | A/G | 0.00194459 | 0.031121 | missense | DCAF4 | GRCh38.p7 | 14:72951866 | CATCACTGTTCGTCA[A/G]TAGTCACCCAGGTAC | 26094 |
rs7156296 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952065 | TTACCCATCTTGGGC[C/T]ATTTCAGTCATTTCA | 26094 |
rs7160796 | snp | C/G | 0.370568 | 0.219005 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927906 | ATGTTGTTTTACAGT[C/G]AACAACTCCTAACTg | 26094 |
rs7160837 | snp | C/G | 0.267091 | 0.249415 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928060 | cccacctcagcctcc[C/G]aaagtgctgggatta | 26094 |
rs7493034 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962504 | AACACACACACACAC[A/G]CACACACGCATGCAC | 26094 |
rs7493035 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962508 | CACACACACACACAC[A/G]CACGCATGCACACTC | 26094 |
rs7493937 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956952 | GCGCGGTGGCTCACG[C/T]CCGTAATCCCAACAC | 26094 |
rs8003923 | snp | C/T | 0.121369 | 0.214369 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936879 | AATGAGCAAAGGATT[C/T]ATTTAGCAAGAAGAA | 26094 |
rs8004641 | snp | A/G | 0.16911 | 0.236552 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933330 | ctttgggaggccgag[A/G]tgggcagatcacaag | 26094 |
rs8005272 | snp | A/G | 0.101658 | 0.201233 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940881 | CAGGCGTGAGCCACC[A/G]CACCCAGCCTTCTTC | 26094 |
rs8010674 | snp | C/T | 0.493386 | 0.0571263 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962458 | CACTTGAAACCAGCC[C/T]GGGCAACATGCCAAA | 26094 |
rs8022709 | snp | A/C | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936823 | AAAAGGATCTAGGAC[A/C]GAACAATGGAAAGCA | 26094 |
rs9788482 | snp | C/T | 0.443195 | 0.158668 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935197 | GAAAGGTACTGTCTT[C/T]GTCCTAGCCTTTAAA | 26094 |
rs10130567 | snp | C/G | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955220 | GCTTTTGGTGGAGAT[C/G]GAATGCTATCTCTGG | 26094 |
rs10134292 | snp | C/T | 0.169435 | 0.236663 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934488 | AGAGTTGGGGTTTCG[C/T]CATGTTGGTCAGGCT | 26094 |
rs10148121 | snp | A/T | 0.443195 | 0.158668 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935344 | ACTGCAACCTCCGCC[A/T]CCTGGGTTCAAACGA | 26094 |
rs10149638 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953732 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 26094 |
rs10483851 | snp | C/T | 0.17332 | 0.23795 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924632 | TGTCCCCTGGCTCTT[C/T]AGTGGAAAATCCAGC | 26094 |
rs10873253 | snp | C/T | 0.112631 | 0.208878 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928361 | accgcgcccggctaa[C/T]tttttgtattttagt | 26094 |
rs11158993 | snp | C/T | 0.199254 | 0.244796 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928562 | TCACTTTAACTATTA[C/T]AGCATGGTGTAGTAA | 26094 |
rs11158994 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928598 | CTTtatatatatata[A/T]atatatatatatata | 26094 |
rs11158995 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930155 | AAATAAATAAAGTGG[C/T]ATCTCACTGTGGTTT | 26094 |
rs11158996 | snp | C/T | 0.3742 | 0.216966 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930254 | GCTTTTTCTTTTTTT[C/T]TTTTGAGACGGAGTT | 26094 |
rs11158997 | snp | C/G | 0.375399 | 0.216275 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944690 | CCAGCTACTCGGGAG[C/G]CTATGGTGGGAGTAT | 26094 |
rs11158998 | snp | A/G | 0.410061 | 0.192043 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951036 | CCCAGGCTGGAGTGC[A/G]GTCACATGATCACAG | 26094 |
rs11158999 | snp | A/G | 0.409891 | 0.192184 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957119 | CGGAAGTCAGAAGCA[A/G]GAGAATTGCTTGGAC | 26094 |
rs11273176 | in-del | -/GCCGTATCCTGGGGCTCTTCCCGGCA | 0.350982 | 0.228698 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942604 | GCGAAACAAGAGGCG[-/GCCGTATCCTGGGGCTCTTCCCGGCA]GCCGTATCCTGGGGC | 26094 |
rs11288108 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937430 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGTCTTGC | 26094 |
rs11428949 | in-del | -/G | 0.4944 | 0.0526182 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928977 | CAAGCCTACCTCCCA[-/G]GGGGAGGCGAGGCCA | 26094 |
rs11463723 | in-del | -/T | 0.375 | 0.216506 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940974 | AACTGTTTTTTGGGG[-/T]TTTTTTTGAGACAGG | 26094 |
rs11621489 | snp | C/T | 0.372592 | 0.217879 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941148 | TTTGTATTTTTTTTA[C/T]AGAGATGGAGTTTCA | 26094 |
rs11624935 | snp | A/G | 0.495016 | 0.0496707 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927972 | ATTTTTAAATTATTT[A/G]TTAAGATGGGGCGGA | 26094 |
rs11625632 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933492 | tgaacccaggaggca[G/T]aggttgcagtgagcc | 26094 |
rs11626756 | snp | C/T | 0.32885 | 0.23724 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934449 | GTGAGCCACTGCACC[C/T]GGCCTAATTTTTGTA | 26094 |
rs11626863 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934668 | TGGAGCAGTCACTCC[C/T]TTCTCTCCCACCACA | 26094 |
rs11627982 | snp | C/T | 0.362732 | 0.22314 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935443 | TACTTTTAGTAGAGA[C/T]GGGGTTTCACCACGT | 26094 |
rs11844136 | snp | A/G | 0.00493321 | 0.0494193 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954353 | CAGACTACATGTGAC[A/G]TAATCTTACCAGCCC | 26094 |
rs11849948 | snp | C/G | 0.0228947 | 0.104514 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959331 | TTTGGAATCCTTAAA[C/G]TTGGCCTTCTCAAAC | 26094 |
rs11851332 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951669 | GGCAGTGTAAACGCA[C/T]GTTGAATCTGGACGG | 26094 |
rs12434259 | snp | A/G | 0.157311 | 0.232183 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957701 | TAATAAACTGCAGCC[A/G]GGATTCAGCTTCAGC | 26094 |
rs12435700 | snp | A/C | 0.362523 | 0.223246 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934943 | GCTTTGCTTCAGTTC[A/C]GCAAAAATTTACTAA | 26094 |
rs12435866 | snp | C/G | 0.37138 | 0.218556 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929533 | AGCGAGACCCCGTCT[C/G]TACAAAAATATTTTT | 26094 |
rs12436610 | snp | C/G | 0.15698 | 0.23205 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943249 | GATTTTAACCTGCCT[C/G]CTGGCTACCCGCTGG | 26094 |
rs12436726 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953517 | gagttcaagaccagc[C/T]tgagcaacatagcaa | 26094 |
rs12586767 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937682 | cctcggcctcccaaa[A/G]tgctgggattacagg | 26094 |
rs12587742 | snp | A/G | 0.349671 | 0.229272 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926683 | GGGAGGAGTGAGCAC[A/G]TGGAACGCCGGCGCC | 26094 |
rs12587782 | snp | C/G | 0.409891 | 0.192184 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957104 | AATCTCTCAGCTACT[C/G]GGAAGTCAGAAGCAG | 26094 |
rs12588961 | snp | A/C | 0.362732 | 0.22314 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934239 | GCTCACGGCAACCTC[A/C]ACCTCCCGGGTTCAA | 26094 |
rs12878126 | snp | C/T | 0.242201 | 0.249878 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927994 | TGGGGCGGAGGGGTG[C/T]CTCACTATGTTGCCC | 26094 |
rs12881839 | snp | A/T | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[A/T]TATATATATATATAT | 26094 |
rs12882409 | snp | A/G | 0.282286 | 0.247906 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958754 | CTCCCGGGGCGCGCC[A/G]GGGCTGCTCATGGCT | 26094 |
rs12885192 | snp | C/T | 0.439224 | 0.163383 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932998 | cctgcctcggcttcc[C/T]gagcagctgggatta | 26094 |
rs12885397 | snp | A/G | 0.435407 | 0.167703 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941426 | CACCACGGGTGGAAT[A/G]GAGAGTGGTGCAGAC | 26094 |
rs12886647 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955980 | cgggctggagtgcag[A/T]ggtactatcttggct | 26094 |
rs12892806 | snp | C/G | 0.493969 | 0.05458 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936225 | GATCCATAGGGAAAC[C/G]CACACATGGTGTTCA | 26094 |
rs17122570 | snp | C/T | 0.0547245 | 0.156101 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933973 | CTTGTCACCCCATGC[C/T]GCTGCCTTTCAGGTG | 26094 |
rs17122577 | snp | A/G | 0.362732 | 0.22314 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936119 | TAACACTGGCCACAC[A/G]TGCTTCCCTTCCTGT | 26094 |
rs17122581 | snp | C/T | 0.362732 | 0.22314 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936613 | GCAGGGGCAGGGATA[C/T]TGCTTTCAGAGAAGA | 26094 |
rs17122598 | snp | C/T | 0.0112964 | 0.0743008 | synonymous-codon, missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938062 | CAGACTCCGTGATTC[C/T]GAAGACAGGCAAGTG | 26094 |
rs17122607 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938369 | AAGCTAGAGGTAGAC[A/G]TTATCTGAAACAACT | 26094 |
rs17182090 | snp | C/T | 0.24449 | 0.249939 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925388 | TCAAGCTTCATGAAG[C/T]GGTTCTTTATTCTGA | 26094 |
rs17569391 | snp | C/G | 0.157311 | 0.232183 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959359 | AACTCAGCAGCAGAT[C/G]TCCGGGATTCTGCTG | 26094 |
rs17781739 | snp | G/T | 0.25045 | 0.25 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926131 | GACTTCTCCAGGGCC[G/T]CATCACCCTGCGGAG | 26094 |
rs17781758 | snp | C/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933664 | CTTTCAAATCTGTCT[C/T]TTTAGGCTCAATTTC | 26094 |
rs17856582 | snp | A/C | 0.0920263 | 0.193764 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945927 | CAGTGAACGATGTTA[A/C]AGTTGGAGGCTCCAA | 26094 |
rs17856583 | snp | C/T | 0.040311 | 0.136127 | intron-variant, missense | DCAF4 | GRCh38.p7 | 14:72954478 | GCCCAGCAGTTTGCT[C/T]TCATGGTTGGTTGGA | 26094 |
rs17856584 | snp | A/G/T | 0.277778 | 0.248452 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958633 | AGGACTGCTACACGA[A/G/T]AATCTGGAGCCTCCA | 26094 |
rs28372931 | snp | A/T | 0.317451 | 0.240729 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926255 | ACCCCCAAGCGCTCC[A/T]TGACCAGCCTCCACG | 26094 |
rs28374876 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933080 | TGGAAGCTGCCCTGC[A/G]CATTGTAGGGTGGTT | 26094 |
rs28393070 | snp | A/G | 0.32955 | 0.237006 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937582 | CACGTTACAACTCCC[A/G]GCTAATTTTTGTATT | 26094 |
rs28583851 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950982 | CTTTTTGGGCTTTTT[A/T]ATAGTATTTTATTTT | 26094 |
rs33999698 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957363 | GCTATAGCGTAATCA[-/G]GACAGTGTGCAGGCT | 26094 |
rs34055762 | snp | A/G | 0.00316069 | 0.0396277 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943011 | TAGCCCACGAGCTGC[A/G]TCTCAGCTGCATGGA | 26094 |
rs34251756 | in-del | -/A | | | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72954458 | GACCAACAGTGATGT[-/A]CTTGGCCCAGCAGTT | 26094 |
rs34392033 | in-del | -/A | 0.455858 | 0.141853 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945475 | TTTTTTCATGGTGGT[-/A]AAAAAAAAAAAAAAT | 26094 |
rs34401726 | in-del | -/A | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933559 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 26094 |
rs34405281 | in-del | -/TAGTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953762 | ATATATATATATATA[-/TAGTTT]ATTTATTTATTTATT | 26094 |
rs34433136 | snp | C/T | 0.362523 | 0.223246 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932710 | ACAGGTTTTCTCAGC[C/T]TTAGCACTGTTTTGG | 26094 |
rs34640207 | in-del | -/A | | | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72956412 | GACCTGAGGACCACG[-/A]AAGTGCGTAAGGCAG | 26094 |
rs34676562 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960173 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGTTTTAT | 26094 |
rs34697676 | in-del | -/C | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958952 | GAAGTGCTGAATGTT[-/C]CCGTGTGGAGATGCT | 26094 |
rs34742859 | in-del | -/A | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926767 | GGGCCCTCCGGCCGG[-/A]ATCAGTGCTGCAACC | 26094 |
rs34917327 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952992 | CCACAATGCCCGGCC[-/T]TTTTTTTTTTTTTTT | 26094 |
rs34981002 | in-del | -/TT/TTT | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935270 | ATGATTTTTTTTTTT[-/TT/TTT]GAGACGGAGTTTCAC | 26094 |
rs35038774 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951164 | TTTGTATTTTTTGTA[-/G]GAGACAAGGTTTTGC | 26094 |
rs35058095 | in-del | -/T | 0.398534 | 0.201091 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950811 | TGCCATTTCTGTATG[-/T]TTTTTTTTAAACAAA | 26094 |
rs35071895 | in-del | -/A | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926768 | GGGCCCTCCGGCCGG[-/A]TCAGTGCTGCAACCG | 26094 |
rs35162447 | in-del | -/G | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959740 | CTGGAGAGCTTCCCT[-/G]GGGCCCCTCCAGACC | 26094 |
rs35165982 | in-del | -/T | 0.375996 | 0.215928 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960158 | CTATAAAGAACCAAA[-/T]TTTTTTTTTTTTTTT | 26094 |
rs35207156 | in-del | -/C | 0.22263 | 0.248497 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933140 | GCTAGTAGCAGCCTA[-/C]CCCCTCCTTCTCCCG | 26094 |
rs35407297 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946984 | GGTTACTTCCTGTCC[-/A]TGCTTAAGCCCCACC | 26094 |
rs35481507 | snp | C/T | 0.00907736 | 0.0667554 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958656 | AGCCTCCACGATGCC[C/T]GCCTACTGAGAACCA | 26094 |
rs35590602 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942487 | AGGGCCCCTTCAGGG[-/G]AAGGCCAGAAACACC | 26094 |
rs35646099 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946551 | AGGACCGTCCCTCCA[-/G]GGGTCCAGGAGTTGA | 26094 |
rs35791547 | in-del | -/T | | | frameshift-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72958676 | CTGAGAACCATACCC[-/T]TCCCCGTACCCTGCC | 26094 |
rs35802342 | snp | A/G | 0.000485285 | 0.0155694 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939871 | GTCTCCGTCAACCTC[A/G]TCTGGCACAGCTGGG | 26094 |
rs35815545 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947211 | CCTTTGGCAGAGGAA[A/G]AGGTTTGGTGGGCAG | 26094 |
rs35885360 | in-del | -/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933233 | TTAAGAAGCACTGAT[-/G]CTACAAACTGTGATG | 26094 |
rs36054756 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928490 | TGAGCCACCGCGCCC[-/G]GGCCAGTCTACAGAC | 26094 |
rs36084134 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961296 | CCGCTCTTCCCAACT[-/G]CTGAAGCCCCTGTTC | 26094 |
rs36177817 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935228 | TCTTACTGTATTTGG[-/C]AAGGCTTCTATTAGT | 26094 |
rs36179699 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935189 | AGTACTAGAAAGGTA[-/C]CTGTCTTCGTCCTAG | 26094 |
rs41317308 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956885 | ACATTTCCACCAGAG[A/G]ATGCTGAGAAAAGAA | 26094 |
rs45514791 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957526 | ATTACTTTGTTAGGA[C/T]ATTCATAGACTTATT | 26094 |
rs45602739 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959574 | TTTGTAATCTAGGAG[C/T]GACAGTTCGTGAGAT | 26094 |
rs55793750 | snp | A/T | 0.15698 | 0.23205 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945491 | AAAAAAAAAAAAAAT[A/T]GTGCCTATGTAATAG | 26094 |
rs56065318 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928597 | CCTTTATATATATAT[-/A]TATATATATATATAT | 26094 |
rs56344374 | snp | C/T | 0.364817 | 0.222075 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938863 | ATTACTGTATGCTAG[C/T]GTAGACTTTAAAACC | 26094 |
rs56683761 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946265 | TTGAGTGTGGTGGCG[C/T]GCACCTGTAGTCCCA | 26094 |
rs56820568 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960926 | TCTGTCGCCCAAGCT[A/G]GAGTGCATGAGTTGC | 26094 |
rs56832550 | in-del | -/CTC | 0.380529 | 0.213219 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954555 | CAGATTGAAATTGGA[-/CTC]CTCTGTGTGCCATCT | 26094 |
rs56871190 | in-del | -/AT/TA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930642 | TGTATATATATATAT[-/AT/TA]GTAGTGTGTGTGAGT | 26094 |
rs56905972 | snp | A/T | 0.157311 | 0.232183 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952752 | CAGGCTGGAGTGCAA[A/T]GGCACGATCTCAGCT | 26094 |
rs56991555 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939715 | GAGGTGAAGGCTGCA[A/G]AACTGCCCGAATGGA | 26094 |
rs57097782 | snp | A/G | 0.157311 | 0.232183 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953253 | GATCCACCCGCTTCG[A/G]CCTCCTAAAGTGCTG | 26094 |
rs57258334 | in-del | -/TATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928612 | ATATATATATATATA[-/TATATA]GTTCACATACCCTAA | 26094 |
rs57515626 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930247 | TTCTTTTTTTTTTTT[-/T]GAGACGGAGTTTTTT | 26094 |
rs57597263 | in-del | -/CGCT | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962514 | ACACACACACACGCA[-/CGCT]TGCACACTCTCTCTC | 26094 |
rs57625319 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936798 | ATGAGGTGGTGTTAA[A/G]TCTGAAAAGAAAAGG | 26094 |
rs57682131 | snp | A/G | 0.161267 | 0.233723 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960275 | CTGCCTCAGCCTCCC[A/G]AGTAGGTTGGATTAT | 26094 |
rs57911111 | snp | A/C | 0.410568 | 0.191619 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954576 | TGTGTGCCATCTAGT[A/C]CTCTTTGACAGGGGA | 26094 |
rs58293765 | in-del | -/TT/TTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953017 | TTTTTTTTTTTTTTT[-/TT/TTTTT]GAGATGGAGTTTCAC | 26094 |
rs58637962 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954643 | AAGGGTGTCTGAGCC[A/G]AGTGAAAGTTGGTTG | 26094 |
rs58705908 | snp | G/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958886 | GCATCTAATGAGGGT[G/T]TTTTAAGTGACACTC | 26094 |
rs59141588 | snp | C/T | 0.18989 | 0.242666 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952928 | TCGAACTCCTGACCT[C/T]GTGATCCACCTGCCT | 26094 |
rs59287534 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936564 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 26094 |
rs59335829 | in-del | -/T/TTT | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931281 | TTTTTTTTTTTTTTT[-/T/TTT]GTAACTGAGCCTGAG | 26094 |
rs59591876 | snp | C/T | 0.155325 | 0.23138 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952907 | ACCATGTTGGTTAGG[C/T]TGGTCTCGAACTCCT | 26094 |
rs60174440 | in-del | -/T/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940608 | TTTTTTTTTTTTTTT[-/T/TT]GAGGCGGAATCTCAC | 26094 |
rs60339019 | snp | A/G | 0.103082 | 0.202275 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926285 | GTGCATCCGCCCCAG[A/G]CAGGCCAGGCCTGGG | 26094 |
rs61291567 | in-del | -/TT/TTT | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934170 | CTTTTTTTTTTTTTT[-/TT/TTT]GAGACGGAGTCTCGC | 26094 |
rs61365507 | snp | C/T | 0.362732 | 0.22314 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935766 | GGACACAGTCCTGCC[C/T]CCTGTGGGTGATCTG | 26094 |
rs61447589 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932597 | AAAGGCAAGCCCAAC[C/T]TTCTGCAACACACCT | 26094 |
rs61746594 | snp | G/T | 0.0122225 | 0.077213 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939874 | TCCGTCAACCTCGTC[G/T]GGCACAGCTGGGACC | 26094 |
rs61988513 | snp | A/C | 0.0240643 | 0.107019 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926220 | AGCCCCCGGCCCCGC[A/C]CCCGCGTGCGCCTGG | 26094 |
rs61988541 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927375 | TTTTTTTTTTTTGAG[G/T]CGGAGTCTCGCTGTC | 26094 |
rs61988542 | snp | A/G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928599 | TTTATATATATATAT[A/G/T]TATATATATATATAT | 26094 |
rs61988543 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928976 | GTCAAGCCTACCTCC[C/T]AGGGGAGGCGAGGCC | 26094 |
rs61988544 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930529 | CAGTCCCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 26094 |
rs61988545 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938524 | GCATTCTGAGGAATA[A/T]GTTGTTAGGCAGTCG | 26094 |
rs61988546 | snp | A/G | 0.0953349 | 0.196415 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940413 | CCCCCTGTCCTCTCC[A/G]CTCCTGCCAGCACCT | 26094 |
rs61988547 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943859 | GTGGGACTGGAGGCC[A/G]ATGCTAGAGATTGAC | 26094 |
rs61988548 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943961 | TGGGGACCGGGCCCA[C/T]ATTCTCCCATGTGGC | 26094 |
rs61988549 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952577 | AATTTGTCTTACAAA[A/T]GTAATTTTTAGTGTT | 26094 |
rs61988550 | snp | A/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953883 | GGTGATCGAGGATCG[A/G]AGCCACCTTACCTCC | 26094 |
rs61988551 | snp | C/T | 0.0418186 | 0.138422 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961664 | GGAAGCCTTCTGTCC[C/T]TCAACCTCACCAGCC | 26094 |
rs66539546 | in-del | -/AGAT | 0.101658 | 0.201233 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937228 | AACATATGGGGGAAC[-/AGAT]AGATGTCTGCAGTTC | 26094 |
rs67150216 | in-del | -/TATATATATA | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928608 | TTAGGGTATGTGAAC[-/TATATATATA]TATATATATATATAT | 26094 |
rs67527791 | snp | A/G | 0.410399 | 0.191761 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952552 | AGGAAACTGAGGCAG[A/G]CAGTTTCAGAATTTG | 26094 |
rs71109769 | in-del | -/ATATATATAT | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953752 | AAACTATATATATAT[-/ATATATATAT]ATATATATATATATA | 26094 |
rs71109770 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955915 | AAAAAAAAAAAAAAA[-/A]GGACATAACCAGAGA | 26094 |
rs72429674 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934157 | TACGTGGCATTTTCT[-/TTT]TTTTTTTTTTTTTGA | 26094 |
rs72472806 | in-del | -/GGTAGTT | 0.161948 | 0.23398 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946073 | ACACTTGACCCTGGG[-/GGTAGTT]GGCCAAATTCAGGGT | 26094 |
rs72732496 | snp | C/T | 0.328616 | 0.237317 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933142 | CTAGTAGCAGCCTAC[C/T]CCTCCTTCTCCCGAG | 26094 |
rs72734407 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949868 | GTCATTCAGACAACA[C/G]CTATCGAGTATATGC | 26094 |
rs72734410 | snp | A/G | 0.485528 | 0.0838238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953826 | TGTGTGTGTGTGTGT[A/G]TGTATATACACACAC | 26094 |
rs73309964 | snp | G/T | 0.49614 | 0.0437598 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940591 | CTTGTTCGATAAGTT[G/T]TTTTTTTTTTTTTTT | 26094 |
rs73309968 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942933 | GGAAGGCCAGAGACC[C/T]CCGAATCTTCTTCAT | 26094 |
rs73309970 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943514 | CCTTTGGTCACTAGA[A/G]GGTAGGACTCCTTGC | 26094 |
rs73309971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943750 | AGAGCAGGGCCTGCC[C/T]GGCAAGCCCTATCCT | 26094 |
rs73309980 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957399 | CTTTCACACTGAAAT[A/G]GTAGCTGCTGACACT | 26094 |
rs74060897 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929532 | AAGCGAGACCCCGTC[C/T]CTACAAAAATATTTT | 26094 |
rs74060902 | snp | A/C | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934912 | TTAAATGTAAAGTAG[A/C]CACAGGTTTTGTTTT | 26094 |
rs74062604 | snp | G/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936849 | AAGCACATACAGGGT[G/T]TGTGACCCAGGAGAA | 26094 |
rs74062605 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938533 | GGAATATGTTGTTAG[A/G]CAGTCGTGTCATGCA | 26094 |
rs74062607 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941578 | GGCCTTTCCTCTTGC[C/T]GAGGAAGGGAGACTT | 26094 |
rs74062610 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942002 | CCCACCCTGAGAAAG[C/T]TGTTCTCTCTAGAGC | 26094 |
rs74062612 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942638 | CCCGGCAGCCGTATC[C/T]TGGGGCTCTTCCCAG | 26094 |
rs74062613 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951715 | CCTAGGTTGTGTGCC[A/G]TATGACTTTCTGAAG | 26094 |
rs74675335 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955277 | ACAGTGCAGGGGGGT[C/G]GGGGGCAGCTCCTAG | 26094 |
rs74752514 | snp | C/T | 0.0426913 | 0.139725 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949145 | TACACATCACATACT[C/T]AGATAGTCAAGAATG | 26094 |
rs74920642 | snp | G/T | | | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958771 | GGCTGCTCATGGCTG[G/T]CGGGCAGGACCTTTA | 26094 |
rs74939138 | snp | A/C | 0.15698 | 0.23205 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944337 | GAACATAACTTCTTC[A/C]TGAGTAAACTTACAA | 26094 |
rs75033229 | snp | C/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931988 | CCTATATTTTTCCTT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs75234653 | in-del | -/A | 0.432797 | 0.170544 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962181 | AGGAGGTGAGACGAG[-/A]AAGGGCTTCTCAGGC | 26094 |
rs75235666 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942456 | CTTCCTGGGGCACAG[C/T]CCTCGGACCTTGGAG | 26094 |
rs75298001 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959130 | GAAGATTGGCAAAAA[C/T]GAAAAGCTTCTTCCT | 26094 |
rs75711974 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929216 | GAGCCTGTAATTCCG[G/T]AAGCTGCGGGCTCCC | 26094 |
rs75773648 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950958 | GGACTAGGGAGGGAT[C/T]AGAGAGGGCTTTTTG | 26094 |
rs75774911 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930713 | CCTAATCAAGATCAT[A/G]ATGATTTATACCTTT | 26094 |
rs76063118 | snp | A/C | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931732 | AATGTTTTTTTAATC[A/C]TGAGAGGATGTTGCA | 26094 |
rs76179085 | snp | C/T | 0.031825 | 0.122064 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944389 | ACCAACGTCCAAACT[C/T]GTGTGTGGGTCTGTA | 26094 |
rs76201553 | snp | G/T | 0.118933 | 0.212888 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945463 | TCAATGCAATTTTTT[G/T]TTCATGGTGGTAAAA | 26094 |
rs76245477 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947592 | TGCCGGAGGGCTGGT[A/G]TGGTAGCAGAGGAAC | 26094 |
rs76295055 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938759 | GATTTTTTTTTAAAT[A/G]GTATACCTATGTATG | 26094 |
rs76310328 | snp | A/G | 0.00155681 | 0.0278564 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958770 | GGGCTGCTCATGGCT[A/G]TCGGGCAGGACCTTT | 26094 |
rs76342307 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949221 | TGGGAGGCCAAAGTT[G/T]GGGGATTGCTTGAGG | 26094 |
rs76368243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947073 | ACGTCTGTGTCCCCA[C/T]ATGTTATTCCACAGG | 26094 |
rs76485499 | snp | G/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952025 | TACCAGAAGCATGTG[G/T]TTTTTTTACAGCATC | 26094 |
rs76866015 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948119 | TCCTCGACAAATGAT[A/T]ACTGAATCAGGATCT | 26094 |
rs76891117 | snp | A/G | 0.171704 | 0.237423 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933129 | TACCCACTAGGCGCT[A/G]GTAGCAGCCTACCCC | 26094 |
rs76948178 | in-del | -/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928185 | CTACAGAATCCCCCC[-/TT]ACTTTTTTTTTTTTT | 26094 |
rs77141854 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924767 | CACTACCTTTCACAA[G/T]GACTGTTGCTGCAAT | 26094 |
rs77152358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960557 | TGTGCCCCCTCAGCA[C/T]TGTGGCTGACAGTCT | 26094 |
rs77222663 | in-del | -/AAAAAAAAA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946237 | CTCTACAAAAAAAAA[-/AAAAAAAAA]TTATTTGAGTGTGGT | 26094 |
rs77556503 | snp | C/G | 0.0264622 | 0.111941 | missense | DCAF4 | GRCh38.p7 | 14:72955546 | GCTGTTTAATGGCTG[C/G]CGCTCTGGGGAAATC | 26094 |
rs77626167 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931873 | TCTGAGATAAATCGC[A/G]CTTGGTCTTGGTATA | 26094 |
rs77694099 | snp | A/G | 0.170408 | 0.236992 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931738 | TTTTTAATCATGAGA[A/G]GATGTTGCATTTTGT | 26094 |
rs77818935 | snp | A/T | 0.104504 | 0.2033 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944782 | GGGCAACCAATCAAG[A/T]CTCTGTCTCAAGAGA | 26094 |
rs77903350 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937202 | AGCTGAGATAAGGAG[A/G]AGGAGACATTAACAT | 26094 |
rs77923831 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940982 | TTTTGGGGTTTTTTT[G/T]AGACAGGGTCCCACT | 26094 |
rs77972595 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960506 | AGGCTCTGACCTCTT[A/C]CTTCTCCCACCAGCA | 26094 |
rs78047397 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936858 | CAGGGTGTGTGACCC[A/G]GGAGAAATGAGCAAA | 26094 |
rs78174515 | snp | A/G | 1.65125e-05 | 0.00287333 | missense | DCAF4 | GRCh38.p7 | 14:72955557 | GCTGCCGCTCTGGGG[A/G]AATCTTTGCCATTGA | 26094 |
rs78555598 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950243 | CTGCAAGACTAAGGG[C/T]GGTGGTGAGGGCGTG | 26094 |
rs78636128 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950819 | CTGTATGTTTTTTTT[A/T]AAACAAAAGCTGCTT | 26094 |
rs78999767 | snp | C/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930245 | ATTTGTGTAGCTTTT[C/T]CTTTTTTTTTTTTGA | 26094 |
rs79069787 | snp | A/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946247 | AAAAAAAAAAAAAAT[A/T]ATTTGAGTGTGGTGG | 26094 |
rs79278829 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946660 | GCCCTGTGTGTCAGA[C/G]TGATGCGTCATCCAG | 26094 |
rs79368931 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925714 | CAAGCCCATCAGAGG[C/T]TTCCGTTTTCCTTTC | 26094 |
rs79434383 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937231 | ATATGGGGGAACAGA[C/T]AGATGTCTGCAGTTC | 26094 |
rs79442944 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929956 | CTCCATGGCGGCCGT[A/G]GCGGAAGGCCAAAAA | 26094 |
rs79475239 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958516 | GCTCACATGAAATCA[A/C]AGCCCTGAGGAATCT | 26094 |
rs79480529 | snp | C/G | 0.131038 | 0.219882 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941908 | TAAGAATCCAGTCTG[C/G]ATAGACCATGTGGCT | 26094 |
rs79688793 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937420 | CTTTTCTTTTTTTTT[C/T]TTTTTTTTTTGAGAT | 26094 |
rs79762499 | snp | A/T | 0.0418186 | 0.138422 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935158 | CACACTCCCCACCCC[A/T]GAACAGGCTTCTTAA | 26094 |
rs79768573 | snp | G/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932001 | TTCTTTTTTTTTTTT[G/T]TTTGAGAGATGGAGT | 26094 |
rs79855068 | snp | A/G | 0.0115144 | 0.0749975 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962106 | GTCTCCAAGTGTGCC[A/G]TTTCTTCCCTGAGAC | 26094 |
rs80246422 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938928 | TTTAAGAGATGAGGT[C/G]TCACTCTGTTGCTCA | 26094 |
rs80263818 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952206 | TGCTATCAGGGATAC[G/T]TAACAGTCTGCCTAC | 26094 |
rs80346534 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926132 | ACTTCTCCAGGGCCG[C/T]ATCACCCTGCGGAGG | 26094 |
rs111236664 | snp | A/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931080 | TTTCAAGATGATTTT[A/G]GGTATTCTGGGTCCC | 26094 |
rs111537843 | snp | A/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945789 | CTAGTGAAAATGCAC[A/G]GAGCATGGGGGCCAG | 26094 |
rs111644671 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957163 | GTTGCAGTGAGCCGA[C/T]ATCACGCCACTGCAC | 26094 |
rs111657988 | snp | A/G | 0.000396609 | 0.0140765 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945855 | GGCGCAGCCTGGGAC[A/G]TCACCCACTGCCCCC | 26094 |
rs111912665 | snp | A/G | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942629 | GGGGCTCTTCCCGGC[A/G]GCCGTATCCTGGGGC | 26094 |
rs112012187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934500 | TCGTCATGTTGGTCA[G/T]GCTGGTCTCAAACTG | 26094 |
rs112070746 | snp | C/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945657 | CCCTCACTGCCATTC[C/T]CATCCTTCCTCTTGA | 26094 |
rs112072118 | snp | A/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956510 | TGGCAGGTACTTGAG[A/G]AAGGAAGGGGAAGTT | 26094 |
rs112256014 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947060 | AGAGAGAAGTCACAC[A/G]TCTGTGTCCCCACAT | 26094 |
rs112623117 | in-del | -/T/TT | 0.320575 | 0.239832 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930246 | TTGTGTAGCTTTTTC[-/T/TT]TTTTTTTTTTTTGAG | 26094 |
rs112776258 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925569 | CCCCACCGCCTGCTT[C/T]CTAACGGGTCCAAGC | 26094 |
rs112783045 | snp | A/G | 3.43536e-05 | 0.00414435 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942957 | TCTTCATGGATGTCA[A/G]CTTCAGCATCCATGC | 26094 |
rs112784300 | in-del | -/TT/TTT/TTTT | 0.123105 | 0.215401 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935261 | TGACTTTTTAAATGA[-/TT/TTT/TTTT]TTTTTTTTTTTGAGA | 26094 |
rs113024126 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929847 | CAGACGCCCGCGGCG[G/T]CGGCTGTGCCTGGGC | 26094 |
rs113094679 | in-del | -/AC/ACACACAC/ACACACACACAC | 0.5 | 0 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962489 | CCCTGTCTTTACAAA[-/AC/ACACACAC/ACACACACACAC]ACACACACACACACA | 26094 |
rs113144096 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943268 | GCTACCCGCTGGGAG[A/C]CGCTGAGCTGGCAGG | 26094 |
rs113214080 | snp | C/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940889 | AGCCACCACACCCAG[C/G]CTTCTTCAGCAGTTC | 26094 |
rs113319103 | snp | G/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940970 | TTAGTAACTGTTTTT[G/T]GGGGTTTTTTTGAGA | 26094 |
rs113491151 | snp | C/T | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943526 | AGAGGGTAGGACTCC[C/T]TGCTTGCCGCCCCTG | 26094 |
rs113559574 | snp | A/G | 0.5 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945617 | GTGAGGTCCTCATGC[A/G]GACCTCAGACTTTCT | 26094 |
rs114128363 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960295 | GGTTGGATTATAGGC[A/G]CGTGCCACCACGCCT | 26094 |
rs114207693 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961677 | CCCTCAACCTCACCA[C/G]CCCTTGGCTTTTCAG | 26094 |
rs114219171 | snp | A/C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938754 | TATAAGATTTTTTTT[A/C/T]AAATGGTATACCTAT | 26094 |
rs114222313 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947729 | GGCAAGGTCAGAGAG[A/G]GGGTTCCTTTGGCAG | 26094 |
rs114549902 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933816 | ACTCTACCAGTTATT[C/T]ACTTAACCTTTCTCA | 26094 |
rs114699957 | snp | A/G | 0.029116 | 0.117091 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935278 | TTTTTTTTTTGAGAC[A/G]GAGTTTCACCCTTTT | 26094 |
rs114771374 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944736 | AATCAAAGATGCAGT[C/G]AGCCATGATTGTGCC | 26094 |
rs114799710 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945779 | GAACTCTCACCTAGT[A/G]AAAATGCACAGAGCA | 26094 |
rs114804584 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928416 | CCAGGATGGTCTCAC[A/G]TATCTGCCGACCTCG | 26094 |
rs114865562 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938798 | GTGAACAGAGCTTGC[A/G]GGACTGGAAGTCAGT | 26094 |
rs114910738 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947853 | AAGCAGAGCCACTTT[G/T]CTGAGAGCACGGTAG | 26094 |
rs114958127 | snp | A/G | 0.0437281 | 0.141251 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924555 | CAGAGCCTGCTGGCC[A/G]GCTGCCAGCCACTCA | 26094 |
rs115030418 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940906 | TTCTTCAGCAGTTCT[A/G]ACATTTTGTCATTCC | 26094 |
rs115089562 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949156 | TACTCAGATAGTCAA[A/G]AATGTCACCTGGCCA | 26094 |
rs115243046 | snp | A/G | 0.0298908 | 0.118541 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962213 | TATGCCCTTGCACTC[A/G]GAGAGGCTTCACTTC | 26094 |
rs115326200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947532 | ACTCTGCCACTGTGG[C/T]GTGTGACGGGAGGCT | 26094 |
rs115353703 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942832 | GGGGAAACTCAAATT[C/T]GGATAATCTGGGATC | 26094 |
rs115525890 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942687 | ACCATTGTTTCATCT[C/T]CCGCACTTTCGTCAT | 26094 |
rs115596707 | snp | G/T | 0.0535932 | 0.154675 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962139 | GAGGAAGGAGCCAGC[G/T]GTACTCTCAGCTTCT | 26094 |
rs115668994 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952418 | AAGTGGACAGGGCCT[C/T]CTCAGTCCACATCCG | 26094 |
rs115766558 | snp | G/T | 0.123105 | 0.215401 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926230 | CCCGCCCCCGCGTGC[G/T]CCTGGCCCCACCCCC | 26094 |
rs115814270 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956264 | GCTCAAGAATTCGAG[A/G]TGGAGATCTTCATGA | 26094 |
rs115868434 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940147 | GAGGTGGGGGGACAG[A/G]CCACTGGGCGCCCAA | 26094 |
rs116035473 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937891 | GCTGGTGCTGAGCAT[A/G]AAGCAGCTGCCAAGA | 26094 |
rs116065956 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929298 | TGGAAAACTGCTAGA[C/G]TGTGAGAGAGAGCCG | 26094 |
rs116162901 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947839 | CCTTCCCGGAGAGCA[A/G]GCAGAGCCACTTTGC | 26094 |
rs116380659 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942814 | TCTTCCTGAGCGTTC[C/T]GTGGGGAAACTCAAA | 26094 |
rs116402860 | snp | A/C | 0.0618563 | 0.164627 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961693 | CCCTTGGCTTTTCAG[A/C]CCAGAGGCTCAGGAC | 26094 |
rs116585159 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959982 | ACTTCTATTGGAAAG[C/T]GCTCAGAGAGAGCCG | 26094 |
rs116596122 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935619 | CAGGCTCCCTTACCA[A/G]ATTGCAGTGCCTGTA | 26094 |
rs116605682 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938607 | AGCCACACACACCTA[A/G]GCTATATGGTGTAGC | 26094 |
rs116623136 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955126 | AAAAAAAAAAAAAAA[C/T]TGTGGTCATTACTAT | 26094 |
rs116658044 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947904 | CCTCTGGGACCCTTG[C/G]GGGCTGTTGATATGG | 26094 |
rs116676021 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926882 | CACCCGACACCTGGC[A/G]GGGGCTGGGCTGCGG | 26094 |
rs116769952 | snp | A/G/T | 0.00637247 | 0.0561273 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929078 | CTGCGGGCGGCACGG[A/G/T]CGCCCGGGGCTGCTC | 26094 |
rs116961044 | snp | A/C | 0.0162398 | 0.0886349 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924833 | TCTTTTCTCCCCAAC[A/C]CCCTACACGGTGATT | 26094 |
rs117114876 | snp | C/T | 0.0261563 | 0.111328 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955511 | GGCACTGAGCAGTCC[C/T]TCTTTCCACAGGCTC | 26094 |
rs117355004 | snp | G/T | 0.000724554 | 0.0190198 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947217 | GCAGAGGAAGAGGTT[G/T]GGTGGGCAGGCCACA | 26094 |
rs117447113 | snp | C/T | 0.000576488 | 0.016968 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951782 | GTGCCTAACTGTCCT[C/T]AACAGCTTTTTCCAG | 26094 |
rs117449182 | snp | A/G | 0.0104438 | 0.071504 | missense | DCAF4 | GRCh38.p7 | 14:72954451 | TCCTTTGGGACCAAC[A/G]GTGATGTCTTGGCCC | 26094 |
rs117651766 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959363 | CAGCAGCAGATCTCC[A/G]GGATTCTGCTGTTAT | 26094 |
rs117834087 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946699 | CAGCCAGCACTGAGG[C/T]TTAAACAAATAAGAG | 26094 |
rs117890938 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957143 | CTTGGACCAGGAAGT[C/T]GGAGGTTGCAGTGAG | 26094 |
rs137879065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932439 | CATGTACATTTGTAA[A/G]TTACTTGATAAATAT | 26094 |
rs137886783 | snp | A/T | 0.00835141 | 0.0640778 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962157 | ACTCTCAGCTTCTCT[A/T]ACCCTGGAGAGGAGG | 26094 |
rs137901416 | snp | A/G | 0.154329 | 0.23097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951387 | GAGGCCGAGGCGGGC[A/G]GATCACGTGAGGTCG | 26094 |
rs137991334 | snp | A/G | 3.29783e-05 | 0.00406055 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958653 | TGGAGCCTCCACGAT[A/G]CCCGCCTACTGAGAA | 26094 |
rs138083719 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927741 | TTACGCTGGGTGTGG[C/T]ACCTAGTCCTGTAAG | 26094 |
rs138102563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937761 | AAACTATGTGGTCGA[C/T]TAAGGGTAACAGGAA | 26094 |
rs138104369 | in-del | -/CCTGCCAGTAC | 0.4087 | 0.193169 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960112 | CCCACTTGAATGTTT[-/CCTGCCAGTAC]CCTGACTAATACAGC | 26094 |
rs138232421 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946820 | AAGCTGCAAGATGGA[C/T]ACAGGTTGAAAATGG | 26094 |
rs138258757 | snp | C/T | 0.00123617 | 0.0248306 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939812 | AACAGGTCTGACTCC[C/T]GGGCAGCACAGCCCG | 26094 |
rs138323197 | snp | A/G | 1.6522e-05 | 0.00287414 | splice-donor-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72943097 | TTTAACCTCATACTG[A/G]TGAGTGGGAGGGGGA | 26094 |
rs138338921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952001 | TCCCTAAGCCTGTCC[C/T]AGGGTTAGTACCAGA | 26094 |
rs138346865 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933957 | GCCACTGCAGTTCTT[A/T]CTTGTCACCCCATGC | 26094 |
rs138541438 | snp | A/G | 1.81622e-05 | 0.00301343 | missense | DCAF4 | GRCh38.p7 | 14:72956456 | TGAATGAGTACGCCT[A/G]CCTGCCCCTGCATGT | 26094 |
rs138698378 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961314 | GAAGCCCCTGTTCCC[C/T]TCACTGCTGTGTCCT | 26094 |
rs138935704 | snp | C/G/T | 9.88647e-05 | 0.00703012 | missense, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72946000 | CAAGGTGTTCATGCA[C/G/T]GAAAACCTCTACTTC | 26094 |
rs138992255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948380 | GGTCATAGAGCCTAA[A/G]TACATTAGCGACCTG | 26094 |
rs139025954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944066 | AGCAGCCCCTTCCCT[A/G]GGGTAAAGTGGGTGG | 26094 |
rs139093721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941344 | TGCAATACAGACCAA[C/T]AGGTCTAGACGCTAA | 26094 |
rs139164395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938185 | CTCGTCCCAATGCAG[G/T]TTCTGATTCTGTAGG | 26094 |
rs139228237 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957161 | AGGTTGCAGTGAGCC[A/G]ATATCACGCCACTGC | 26094 |
rs139243326 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924770 | TACCTTTCACAAGGA[C/T]TGTTGCTGCAATAAG | 26094 |
rs139278582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938566 | CATCATAGCACATAC[A/G]TAACACAAACCTACA | 26094 |
rs139381430 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944556 | CCAGCATTTTGGGAG[G/T]CCTCAGCAGGTGGTT | 26094 |
rs139409447 | snp | A/C/T | 0.000362372 | 0.0134563 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940301 | ACTGCAACCCCCTGA[A/C/T]GAAAGAGAGCATCCG | 26094 |
rs139428330 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958728 | GTGGCCTTCTCGTCG[C/T]GGCTGGGGGGCTCCC | 26094 |
rs139579806 | snp | G/T | 3.29462e-05 | 0.00405857 | missense | DCAF4 | GRCh38.p7 | 14:72954217 | CCTGGTGCCTGGTCC[G/T]GTGCCTGGTCCCTGA | 26094 |
rs139629106 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960242 | GCACCCTCCACCTCC[G/T]GGGTTCTAGTGATTC | 26094 |
rs139772335 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958751 | GGGCTCCCGGGGCGC[A/G]CCGGGGCTGCTCATG | 26094 |
rs139905954 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959973 | AAACCCACCACTTCT[A/G]TTGGAAAGCGCTCAG | 26094 |
rs139939011 | snp | A/G/T | 0.0629771 | 0.165899 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953247 | TCAGGTGATCCACCC[A/G/T]CTTCGGCCTCCTAAA | 26094 |
rs139991878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929779 | GCAGCTCGTACGAAG[C/T]GAAGCCACACACCTC | 26094 |
rs140131795 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940791 | AGACAGGGTTTCACC[A/C]TGTTGGCCAGGTTGG | 26094 |
rs140151504 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935165 | CCCACCCCTGAACAG[C/G]CTTCTTAAAAGTACT | 26094 |
rs140196877 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961675 | GTCCCTCAACCTCAC[C/T]AGCCCTTGGCTTTTC | 26094 |
rs140290692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931219 | GTTTTCTGTGTACAC[A/G]CCATATATTAATTTT | 26094 |
rs140335504 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946573 | AGGAGTTGATCTGGA[A/G]GGGCCCACACCAGGG | 26094 |
rs140338863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950412 | TGGGCTACATGGCCA[C/T]AGGGCAGAACTGGAA | 26094 |
rs140377003 | snp | A/G/T | 8.82145e-05 | 0.00664074 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939862 | TGATGACGAGTCTCC[A/G/T]TCAACCTCGTCTGGC | 26094 |
rs140481029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954098 | ATTTGGATGTTTTCC[A/G]AACCCAGTGGTCCCT | 26094 |
rs140507721 | snp | A/G | | | synonymous-codon, splice-acceptor-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940251 | CTTTGACCCTGAAAA[A/G]AAACGCTACTTCCGC | 26094 |
rs140539405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930802 | CCATATGGTATGAAG[G/T]AAGGATCCAAATTCA | 26094 |
rs140545069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951628 | AAAACAAACAAACAA[A/G]AAAAAAACATCTGAA | 26094 |
rs140598805 | snp | A/G | 0.000327166 | 0.0127858 | missense | DCAF4 | GRCh38.p7 | 14:72956419 | AGGACCACGAAGTGC[A/G]TAAGGCAGTACGAAG | 26094 |
rs140685374 | in-del | -/TATATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928586 | GTAGTAAACATCCTT[-/TATATATATATA]TATATATATATATAT | 26094 |
rs140697124 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934298 | AGTGGGGATTGCAGG[C/T]GCCCACTACCATGCC | 26094 |
rs140758661 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930595 | CTTTCGATGCACGGA[A/C]GTTTTCAATTTTGAT | 26094 |
rs140774136 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935422 | ACCACACCCAGTGAA[C/T]TGTTGTACTTTTAGT | 26094 |
rs140803976 | snp | A/G | 1.67365e-05 | 0.00289275 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938031 | GGAGAAGAAGCCACC[A/G]GCAGAACCCTTGGTT | 26094 |
rs140837866 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932477 | TCATTTTCCAAAAAA[A/C]CAAATTGTGTTTATT | 26094 |
rs140933305 | in-del | -/TATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928586 | GTAGTAAACATCCTT[-/TATATATATA]TATATATATATATAT | 26094 |
rs141099828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956616 | GAACTGAATCAAGGG[G/T]AGTGTGGACAGCTGG | 26094 |
rs141191522 | snp | A/C | 0.00130064 | 0.0254681 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945918 | GGCTCTTCACAGTGA[A/C]CGATGTTAAAGTTGG | 26094 |
rs141315052 | snp | A/C/G | 1.64751e-05 | 0.00287007 | missense | DCAF4 | GRCh38.p7 | 14:72955614 | GATGGAAGGCCACCC[A/C/G]CCTGTTTCATGATTC | 26094 |
rs141396040 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938318 | TCTCTGTTCTTTCCT[A/T]AGTGACCACGACCTC | 26094 |
rs141487126 | snp | A/G | 0.15698 | 0.23205 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953621 | AGGCTGAGATGGGAG[A/G]ATTCCTTGAGCCTGG | 26094 |
rs141502610 | snp | C/T | 8.06045e-05 | 0.0063479 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939838 | GCCCGCTCACGATTC[C/T]GGCCACGGTGATGAC | 26094 |
rs141624818 | in-del | -/TG | 0.0174175 | 0.0916809 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931952 | GGATTTTTGTGTCTC[-/TG]TATTCATAACCCATA | 26094 |
rs141716416 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961019 | CAGTCTTCTGAGCAG[C/T]TGGGCCCACAGGTGT | 26094 |
rs141780934 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958955 | AGTGCTGAATGTTCC[A/G]TGTGGAGATGCTCAG | 26094 |
rs141855816 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942747 | CAGACACAACTCCCT[C/G]TAACTCCCACTCTTT | 26094 |
rs142034868 | snp | C/T | 0.00128859 | 0.0253502 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940424 | CTCCGCTCCTGCCAG[C/T]ACCTGTCCATCCACT | 26094 |
rs142053749 | in-del | -/GCTTGGGG | 0.0209421 | 0.100162 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946284 | CCTGTAGTCCCAGCT[-/GCTTGGGG]GCTCGGGGGGAGGTG | 26094 |
rs142071144 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939805 | GTGTGTCAACAGGTC[C/T]GACTCCCGGGCAGCA | 26094 |
rs142103860 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944085 | TAAAGTGGGTGGGGA[C/T]GGTGGGGGTCATTGG | 26094 |
rs142156104 | snp | C/T | 4.94222e-05 | 0.00497078 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941765 | CAGGATGGGATTTAA[C/T]GCATCTTCCATGCTA | 26094 |
rs142240601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948641 | GGAAAAAAAAATCCA[C/T]GTAATTGGACTTAAA | 26094 |
rs142283119 | snp | A/G/T | 0.000115481 | 0.00759792 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946032 | CCAACCGGAAGGTAC[A/G/T]TTGCCCATCCCTGTA | 26094 |
rs142338558 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924424 | CTTGCCCAAGGCCCA[A/G]CAAGCTTCATTTGTT | 26094 |
rs142446297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960450 | CCACCGCACCTGGCC[C/T]GATTCTTAAATATAT | 26094 |
rs142473021 | in-del | -/T | 0.132409 | 0.220618 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924916 | CCTCCCATTGTCTAC[-/T]TTTTTTTTTTCTTGA | 26094 |
rs142503309 | snp | A/G | 0.000446078 | 0.0149278 | missense | DCAF4 | GRCh38.p7 | 14:72954395 | CGCCAGGCTTGTCTC[A/G]GCGGGTCCTGTTGAC | 26094 |
rs142644454 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925589 | CGGGTCCAAGCCGCG[A/G]GCAGGGGCCTGTGTT | 26094 |
rs142676159 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957875 | TGTTGTGTGTCACAG[A/T]CCTCAGAACTGGAGC | 26094 |
rs142780543 | in-del | -/CTC | 0.040671 | 0.13668 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924594 | GCAAGCCCAAGCCAA[-/CTC]CTCCTGCCACCTTCC | 26094 |
rs142782008 | in-del | -/TTTC | 0.329317 | 0.237084 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932881 | GCTGAATAATTTTTT[-/TTTC]TTTCTTTCTTTCTTT | 26094 |
rs142899221 | snp | G/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934496 | GGTTTCGTCATGTTG[G/T]TCAGGCTGGTCTCAA | 26094 |
rs143042729 | in-del | -/CACACACG | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962508 | ACACACACACACACA[-/CACACACG]CACGCATGCACACTC | 26094 |
rs143070109 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927019 | ACATTTGCCAGCGCT[A/G]TGATGTCCTTGTCAG | 26094 |
rs143175478 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932946 | ATCTTGCTATGTTGC[A/G]CAGGCTGGTCTTGAA | 26094 |
rs143346515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952303 | TTAGGATCAATAAGA[C/G]CAGGGTGAGAGGCCT | 26094 |
rs143399351 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959991 | GGAAAGCGCTCAGAG[A/C]GAGCCGGGTTCCAGC | 26094 |
rs143626758 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936752 | GTGCTCAGTAGCGAT[A/G]TTAGGGTTGGAGCTG | 26094 |
rs143663783 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955035 | AGAATTGCCTGAACC[C/T]GGGAGGCGGAGGTTG | 26094 |
rs143663985 | snp | A/G | 0.00250198 | 0.0352807 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938077 | TGAAGACAGGCAAGT[A/G]TGCCGCTCTGGGGAG | 26094 |
rs143732950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942309 | AAGAAGAGACTGAGG[A/C]TCAGAGTGGAGTGAT | 26094 |
rs143817004 | in-del | -/AGA | 0.329317 | 0.237084 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937200 | AAAGCTGAGATAAGG[-/AGA]AGGAGACATTAACAT | 26094 |
rs143822966 | snp | A/G | 0.00145851 | 0.0269653 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939813 | ACAGGTCTGACTCCC[A/G]GGCAGCACAGCCCGC | 26094 |
rs143869522 | snp | A/G | 0.000593442 | 0.0172154 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958657 | GCCTCCACGATGCCC[A/G]CCTACTGAGAACCAT | 26094 |
rs143960756 | snp | A/G | 4.86559e-05 | 0.0049321 | splice-donor-variant | DCAF4 | GRCh38.p7 | 14:72956501 | GAATCCTGGTGGCAG[A/G]TACTTGAGGAAGGAA | 26094 |
rs143968818 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927371 | TTTTTTTTTTTTTTT[G/T]GAGGCGGAGTCTCGC | 26094 |
rs144034897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935279 | TTTTTTTTTGAGACG[A/G]AGTTTCACCCTTTTG | 26094 |
rs144089873 | snp | A/G | 3.43047e-05 | 0.0041414 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958746 | CTGGGGGGCTCCCGG[A/G]GCGCGCCGGGGCTGC | 26094 |
rs144109256 | snp | A/G | 0.000153988 | 0.00877328 | missense | DCAF4 | GRCh38.p7 | 14:72955559 | TGCCGCTCTGGGGAA[A/G]TCTTTGCCATTGATC | 26094 |
rs144277484 | in-del | -/TT | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72935959 | TTTTTCCTATCAGTC[-/TT]TTTCTCTTTTTGAGA | 26094 |
rs144355500 | in-del | -/C | 0.0207874 | 0.0998078 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937931 | AAAAGCCCATGCCCA[-/C]ACACAGAGATGTATG | 26094 |
rs144366256 | snp | C/T | 4.03307e-05 | 0.0044904 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939832 | AGCACAGCCCGCTCA[C/T]GATTCCGGCCACGGT | 26094 |
rs144445116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958555 | CATGTCCACATGTAG[A/G]TAAGTTTTCCTTTGC | 26094 |
rs144502121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950618 | GTCAAAAGACACACA[C/G]GTAGGCAAGGGTATA | 26094 |
rs144512259 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944822 | GGCCAGGTGTGGTGG[C/T]TCACACCTGTAATCC | 26094 |
rs144566588 | snp | A/G | 9.92277e-05 | 0.00704301 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946056 | CCCTGTAGCCTCTCT[A/G]CACACTTGACCCTGG | 26094 |
rs144719098 | snp | A/G | 0.00597534 | 0.0543715 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929077 | ACTGCGGGCGGCACG[A/G]ACGCCCGGGGCTGCT | 26094 |
rs144772772 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925692 | CACAAACTGTCTCTT[A/C]GGGACACAAGCCCAT | 26094 |
rs144784386 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72947190 | TTGGATTCCCACATT[C/T]TGTATCCTTTGGCAG | 26094 |
rs144824364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934487 | TAGAGTTGGGGTTTC[A/G]TCATGTTGGTCAGGC | 26094 |
rs144916703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930662 | ATATATATGTAGTGT[A/G]TGTGAGTTTTGGGTG | 26094 |
rs144984896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949874 | CAGACAACACCTATC[A/G]AGTATATGCAGTTGC | 26094 |
rs145000136 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947810 | TTTTAGAGCACTCAT[C/T]ACACTAGTCTCTGCC | 26094 |
rs145000586 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953246 | CTCAGGTGATCCACC[C/T]GCTTCGGCCTCCTAA | 26094 |
rs145050044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945541 | TGCGCCACAGCCTTC[A/G]TGATGGCACATGACA | 26094 |
rs145062084 | snp | A/G | 0.000758137 | 0.0194549 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940346 | AGAGCAAGAGACTGC[A/G]GCTGCTCCAGGAAGA | 26094 |
rs145192710 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960361 | CTACATGTTGGTCAG[G/T]CTGGCCTCAAACTCC | 26094 |
rs145326670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930112 | CTTCAGCCAAAAGGG[A/G]GGTAGGAGGGAATAA | 26094 |
rs145366170 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925456 | CCGCTCCACATACTG[C/T]ATTTATCTATAAACT | 26094 |
rs145397061 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931883 | ATCGCGCTTGGTCTT[A/G]GTATATAATTCTTTT | 26094 |
rs145491278 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931039 | TTTTGAAATTGCGAG[C/G]TGCGAGTCATCCCAA | 26094 |
rs145594934 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935502 | TCAGGTGATCCACCC[A/G]CATCGGCCTCCCAAA | 26094 |
rs145638558 | snp | C/T | 0.000107665 | 0.00733626 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939810 | TCAACAGGTCTGACT[C/T]CCGGGCAGCACAGCC | 26094 |
rs145655881 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950689 | TGTGAACAGAGACAC[C/T]CACATGTAGTCAGGG | 26094 |
rs145670003 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943017 | ACGAGCTGCGTCTCA[C/G]CTGCATGGAGAGGAA | 26094 |
rs145811130 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926109 | GCTCTTTCCACTACA[A/G]CGAGAGGACTTCTCC | 26094 |
rs145843659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957569 | CAACACCAGGACTTC[A/G]CCTCCTTTTTAAGTC | 26094 |
rs145986879 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941208 | TGGCCTCAAGTAATC[A/C]GCCCACCTTGGCCTC | 26094 |
rs146145409 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943989 | GGCTTTTCTCTCCAT[G/T]TGTGCTTGGGGGTAT | 26094 |
rs146163595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939070 | TAAAATAAAGTTGGC[C/T]GGGCCGGGTGTGGTG | 26094 |
rs146250601 | in-del | -/T | 0.473543 | 0.111932 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931989 | CTATATTTTTCCTTC[-/T]TTTTTTTTTTTTTTT | 26094 |
rs146264573 | snp | A/G | 0.00333497 | 0.0406985 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958727 | TGTGGCCTTCTCGTC[A/G]CGGCTGGGGGGCTCC | 26094 |
rs146364907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944137 | CAGGCCACTGTTCAC[A/C]AGCCTGGACATCTCG | 26094 |
rs146404515 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948838 | TCCTGCAAGAGTGGT[A/G]GGAAGTTAGATGGAA | 26094 |
rs146493974 | snp | A/G | 0.000343177 | 0.0130947 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958749 | GGGGGCTCCCGGGGC[A/G]CGCCGGGGCTGCTCA | 26094 |
rs146504543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938179 | TGGGGGCTCGTCCCA[A/G]TGCAGGTTCTGATTC | 26094 |
rs146567602 | snp | C/T | 0.000906043 | 0.021265 | missense | DCAF4 | GRCh38.p7 | 14:72955577 | TTTGCCATTGATCTG[C/T]GTTGTGGAAATCAAG | 26094 |
rs146805939 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959999 | CTCAGAGAGAGCCGG[A/G]TTCCAGCAACTCTTC | 26094 |
rs147139482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950262 | GGTGAGGGCGTGAAA[C/T]GAGGTATCAGGAGTG | 26094 |
rs147245834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930511 | TGTCCTCAAGTGATC[C/T]GCCAGTCCCAGCCTC | 26094 |
rs147283075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934284 | TCAGCCTCCCAAGTA[C/G]TGGGGATTGCAGGCG | 26094 |
rs147302871 | snp | A/G | 0.00138458 | 0.026275 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958620 | TTCCTAGTGGGCCAG[A/G]ACTGCTACACGAGAA | 26094 |
rs147365709 | snp | A/G/T | 8.23649e-05 | 0.00641683 | missense | DCAF4 | GRCh38.p7 | 14:72954197 | TGCTCTGCAGTTTCC[A/G/T]GATCCCTGGTGCCTG | 26094 |
rs147632262 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945753 | TCATCTCCACTCTCG[A/C]TCATGGAGAGGAACT | 26094 |
rs147735926 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925463 | ACATACTGCATTTAT[C/T]TATAAACTCCTGAGA | 26094 |
rs147775635 | in-del | -/G | 0.040671 | 0.13668 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937001 | CTTTGGCAAGTAGGT[-/G]AATCAATAGCAAGAG | 26094 |
rs147821742 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946517 | GTAGGTTGAAGCAGC[A/G]CTTGTTTAACTGGTC | 26094 |
rs148082977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942716 | ATCTCAGGGGAAGGA[A/G]CTGTACTGAATGATG | 26094 |
rs148135460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948955 | TGAGTATAAATAAGC[C/T]GAGATTCAGCAACAG | 26094 |
rs148227497 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927287 | TAGAGGAAACAATTC[C/T]AAAGTCCCAAACTCT | 26094 |
rs148311071 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955654 | CTCTGTGCGGATCCT[C/T]CAAGATGAGCAATAC | 26094 |
rs148396800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945068 | TACTTCAGCCTGGGC[A/G]ACAGAGTAAGACTCC | 26094 |
rs148601914 | snp | C/T | 1.64936e-05 | 0.00287168 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958672 | GCCTACTGAGAACCA[C/T]ACCCTCCCCGTACCC | 26094 |
rs148641233 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939999 | AGGAGCAAATTGAAA[C/T]ACTCAGGGAAGGAGC | 26094 |
rs148676875 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924352 | TACAACCTTTCTCAG[C/T]AGATGTCTTATCCTC | 26094 |
rs148803415 | snp | A/G | 8.0436e-05 | 0.00634125 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939833 | GCACAGCCCGCTCAC[A/G]ATTCCGGCCACGGTG | 26094 |
rs148869751 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950972 | TCAGAGAGGGCTTTT[G/T]GGGCTTTTTAATAGT | 26094 |
rs148903018 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935553 | AGCCACCACATCCGG[A/C]CTTTAAAATGATTTT | 26094 |
rs148954329 | snp | A/C | 0.000148666 | 0.00862037 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941711 | TAACAAATAAATCTT[A/C]ATTGAATTGTTCTCT | 26094 |
rs149121448 | snp | C/T | 0.00178698 | 0.0298379 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940369 | CAGGAAGAAGACAGA[C/T]GGAAAAAGGTGGGCT | 26094 |
rs149147554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960397 | TCAGGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA | 26094 |
rs149305928 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928556 | TGTTTCTCACTTTAA[C/T]TATTACAGCATGGTG | 26094 |
rs149532947 | in-del | -/TA | 0.383632 | 0.211288 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930641 | GTGTATGTGTGTGTG[-/TA]TATATATATATATGT | 26094 |
rs149574612 | in-del | -/TGTGTGTGTGTG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953783 | ATTTATTTATTTATT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 26094 |
rs149605432 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952143 | ACAGATTCGGACGCC[C/T]GTGCACATCATTCAG | 26094 |
rs149756917 | snp | A/G | 0.000153988 | 0.00877328 | splice-donor-variant, missense | DCAF4 | GRCh38.p7 | 14:72954463 | AACAGTGATGTCTTG[A/G]CCCAGCAGTTTGCTC | 26094 |
rs149835544 | in-del | -/GCCCGCGGCGGCGGCTGT | 0.00755907 | 0.0610114 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929837 | TGCGTTTGCTCAGAC[-/GCCCGCGGCGGCGGCTGT]GCCTGGGCTTGCTCA | 26094 |
rs149878526 | snp | A/G | 0.00011533 | 0.00759287 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940324 | AGCATCCGGCAGAAG[A/G]AGATGGAGAGCAAGA | 26094 |
rs149919379 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953184 | TTTTGTATTTTTAGT[A/G]GAGATGGGATTCTCC | 26094 |
rs150041373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930922 | AGTTGACCATAGATA[A/G]GCATATGGGTTTATT | 26094 |
rs150281699 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956867 | TCCCTGTTGTCTCTA[C/T]TCACATTTCCACCAG | 26094 |
rs150335149 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961928 | GAAGGTTTGGCTACC[A/G]CGGGAACACCCCAGC | 26094 |
rs150351675 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933589 | AGTCTCTAATTCTCA[C/G]TGTATACCATTACCA | 26094 |
rs150423665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946667 | GTGTCAGAGTGATGC[A/G]TCATCCAGCCAGGCC | 26094 |
rs150471266 | snp | C/T | 1.80338e-05 | 0.00300276 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956451 | CCACGTGAATGAGTA[C/T]GCCTACCTGCCCCTG | 26094 |
rs150517676 | snp | A/C/G | 0.00110401 | 0.023472 | missense | DCAF4 | GRCh38.p7 | 14:72954442 | CACCGGCAGTCCTTT[A/C/G]GGACCAACAGTGATG | 26094 |
rs150597366 | snp | G/T | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959970 | CCAAAACCCACCACT[G/T]CTATTGGAAAGCGCT | 26094 |
rs150737233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949638 | CACGCACCCGTAATC[C/T]CAGCTATTCGGGAAG | 26094 |
rs150823618 | in-del | -/C | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935152 | GAAGACACACTCCCC[-/C]ACCCCTGAACAGGCT | 26094 |
rs150825657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938539 | TGTTGTTAGGCAGTC[A/G]TGTCATGCAAACATC | 26094 |
rs150861217 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924696 | TCTCCCTCTGAATTC[C/T]GCCTCCCATCTGTAC | 26094 |
rs150886917 | snp | A/G | 8.05948e-05 | 0.00634751 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939839 | CCCGCTCACGATTCC[A/G]GCCACGGTGATGACG | 26094 |
rs151012011 | snp | C/G | 0.000740803 | 0.0192316 | missense, utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72937999 | TAAAAGTCGCTGGCA[C/G]AGTAGAAGACGACAT | 26094 |
rs151053025 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951377 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 26094 |
rs151089443 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934584 | CGTGAACCACCACGC[C/T]GGGCTTGCCTGACAT | 26094 |
rs151105471 | snp | A/G | 0.126564 | 0.217402 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955946 | TTTTTTTTTTGAGAT[A/G]GAGTCTTGCTCTGTC | 26094 |
rs151208703 | snp | C/T | 0.000658783 | 0.0181372 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941807 | GCTGGGTTTTCTCAA[C/T]GTCACCAATTACTGC | 26094 |
rs180757047 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932641 | AGAGCAGCTCCAAAG[A/G]TGCTAGATGCAGCAT | 26094 |
rs180778842 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952758 | GGAGTGCAATGGCAC[A/G]ATCTCAGCTCACCAC | 26094 |
rs180935817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947540 | ACTGTGGCGTGTGAC[A/G]GGAGGCTCTGGGTTC | 26094 |
rs180945194 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927641 | CAGGCGTGAGCCACC[A/G/T]CGCCCGGCCTGAGGT | 26094 |
rs181018941 | snp | A/C | 0.00013168 | 0.00811312 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956490 | CGAGGAAGAAGGAAT[A/C]CTGGTGGCAGGTACT | 26094 |
rs181020061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936840 | AACAATGGAAAGCAC[A/G]TACAGGGTGTGTGAC | 26094 |
rs181289730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956995 | AGGAGGGTGGATCAC[A/G]AGGTCAGGAGATTGA | 26094 |
rs181483219 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927453 | GCCCCCGGGGTTCAC[A/G]CCATTCTCCTGCCTC | 26094 |
rs181492538 | snp | A/C | 1.66266e-05 | 0.00288323 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958571 | TAAGTTTTCCTTTGC[A/C]TTCTCTCACTAGCCT | 26094 |
rs181515556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938393 | AACAACTGGAAAACC[A/G]TTTCTCCATTTTGTA | 26094 |
rs181687204 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962259 | ATAAGAAGGAGCCAC[A/G]CTATTCATCCTCAAT | 26094 |
rs181694733 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946436 | GGTTGCTGAGAACCC[A/G/T]TAGGGAAAGAAAAGG | 26094 |
rs181697010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934051 | CCTCATGATCATGCC[C/T]TGTCTGCCTCTGCAG | 26094 |
rs181707854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941293 | TAAATAGAAGACCAG[A/G]ATGCATGGTTTGGAA | 26094 |
rs181837144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950901 | GAACTTACACCAATT[C/T]GAGAAGAGCAGTTCT | 26094 |
rs181842104 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953652 | GAGGTTGAGGATGCA[C/T]TGAGCCATGATCACG | 26094 |
rs181846958 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932007 | TTTTTTTTTTTTTGA[A/G]AGATGGAGTCTTGCT | 26094 |
rs182084455 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942890 | TGTGGAGCAGGCTGA[C/T]GAGGAGAGATGGGCG | 26094 |
rs182160475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942458 | TCCTGGGGCACAGCC[C/T]TCGGACCTTGGAGCA | 26094 |
rs182435291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935202 | GTACTGTCTTTGTCC[G/T]AGCCTTTAAACTCTT | 26094 |
rs182479358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948924 | TCTTAGCCTGGCTCC[A/G]TAAGTACTCAAAGTT | 26094 |
rs182492168 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929629 | AGTCTTTCTTGGCAG[A/C]GGCTTTCCTCATGGC | 26094 |
rs182532548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939556 | CAAAATGCGCGAGTG[A/G]GAAGATAAGAAGAGG | 26094 |
rs182544081 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960098 | TAGACTCGCAGTTAC[C/T]CACTTGAATGTTTCC | 26094 |
rs182744035 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959115 | ACTTTTCTAAGGACT[A/G]AAGATTGGCAAAAAC | 26094 |
rs182766567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954632 | GGTTCCTTTGTAAGG[G/T]TGTCTGAGCCGAGTG | 26094 |
rs182842447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960218 | CTGGAGTGCAATGGC[A/G]CTCTCACCGCACCCT | 26094 |
rs182962898 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939175 | TCTGGCCAACACGGC[A/G]AAACTCCGTCTCTAC | 26094 |
rs183292262 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928611 | TATATATATATATAT[A/G]TATATAGTTCACATA | 26094 |
rs183301199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928399 | GGTTTTCACCATGTT[A/G]GCCAGGATGGTCTCA | 26094 |
rs183410715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934581 | AGGCGTGAACCACCA[C/T]GCCGGGCTTGCCTGA | 26094 |
rs183540352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948598 | TCTTAAAACAGCATG[A/G]TATTCTCGTTTCTGT | 26094 |
rs183625683 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924816 | CCAGCTGACTTCCAC[A/G]ATCTTTTCTCCCCAA | 26094 |
rs183729327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945766 | CGCTCATGGAGAGGA[A/T]CTCTCACCTAGTGAA | 26094 |
rs183735296 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925880 | AGAAGAAATCAAGGC[A/T]CAGAGAAGGGAAGAG | 26094 |
rs183837986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943359 | TGGACCCAGCCACAC[C/T]TTGACTACTGAACTT | 26094 |
rs183906952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944907 | CAGCCTGACCAACAT[G/T]GTGAAACCACATCTC | 26094 |
rs184055643 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925075 | CGCCACCACGCCCGG[C/G]TAATTTTTTGTATTT | 26094 |
rs184071368 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937414 | ATTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs184215630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937758 | AGGAAACTATGTGGT[C/T]GACTAAGGGTAACAG | 26094 |
rs184228755 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961738 | TGTTTGGCTGTGGGC[A/G]TGGGGAATGCAGTGA | 26094 |
rs184260364 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940692 | ACCTCCCAGATTCAA[A/G]CAATTCTCCTGCCTC | 26094 |
rs184272030 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940011 | AAACACTCAGGGAAG[A/G]AGCTGGGTGCGTCAG | 26094 |
rs184282020 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931725 | TATGTTGAATGTTTT[G/T]TTAATCATGAGAGGA | 26094 |
rs184376512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956667 | GTAGAATTAGATTAT[A/G]TTAGTAATCAGGAGT | 26094 |
rs184470973 | snp | C/T | 5.07309e-05 | 0.00503616 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955705 | TGGAAAGGTAGGGGA[C/T]CATGGACTTTCTCAG | 26094 |
rs184476876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935565 | CGGCCTTTAAAATGA[A/T]TTTTGCTTGACCTTG | 26094 |
rs184517740 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961565 | GCAAGCTCTGCCAAG[A/C]CCAGAATTTCTGGCC | 26094 |
rs184547558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932203 | TCTATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 26094 |
rs184561403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951071 | CCGCAGCCTTGACTT[C/G]CAAGGCTCAAGCAAT | 26094 |
rs184655877 | snp | C/G/T | 6.58928e-05 | 0.00573957 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940297 | AACAACTGCAACCCC[C/G/T]TGACGAAAGAGAGCA | 26094 |
rs184770124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936521 | GTGAGCTGAGATGGC[A/G]CCACTGCACTCCAGC | 26094 |
rs184789152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956279 | ATGGAGATCTTCATG[A/G]CCTGCACAGGCCACT | 26094 |
rs184859506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949455 | AGAGAGACCCTGTCT[C/G]TTAAAAAAGAGAAAA | 26094 |
rs184902622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930950 | ATTTCTGGTCTCAAT[A/G]CTACTCCATTGATCT | 26094 |
rs185055913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948002 | TGTGTTCTGGAAACA[A/C]TGTGACTACTCATTG | 26094 |
rs185063945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927813 | CAGGGTGGGCGTTAG[C/T]ACAAAGCTTGCGCCT | 26094 |
rs185189633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950622 | AAAGACACACACGTA[A/G]GCAAGGGTATAAAGG | 26094 |
rs185336435 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926782 | GATCAGTGCTGCAAC[C/G]GTAAACACGCAGGGA | 26094 |
rs185514854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958452 | CTAGCACAACAGGGC[A/G]ACTTGGGTTATCCGT | 26094 |
rs185534259 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924392 | TGTGAAGAAACTGAG[A/G]TTGGAATGCCTCATG | 26094 |
rs185549551 | snp | A/C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938236 | GCCTGCCTTCCTAAC[A/C/G]TGCTCCCAGGGCATG | 26094 |
rs186071674 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962342 | TTCCATCAAGAACAG[A/G]GCAAAGGCCAAGCTC | 26094 |
rs186086642 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953666 | ATTGAGCCATGATCA[C/T]GCCACTGCACTCCAG | 26094 |
rs186093533 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934078 | GCAGGCTCATCCCCC[C/G]CATTTCTTGAACTTC | 26094 |
rs186158464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928452 | CGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 26094 |
rs186320026 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948188 | AAAGGAGTTTTTTTG[G/T]ATTTTAATTTTTTTC | 26094 |
rs186358415 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927581 | TGGTCTCGATCTCCT[C/G]ACCTCGTGATCCGCC | 26094 |
rs186436041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952827 | AGCCTCCCAAGTAGC[G/T]GAGATCACAGGCGCA | 26094 |
rs186538839 | snp | C/G | 0.00540715 | 0.051714 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958596 | TAGCCTGCCATGTGT[C/G]TCTCCTCTTTCCTAG | 26094 |
rs186668174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941510 | GTGTATGTGGATGGG[C/G]AGCGTGGGCAGAGTT | 26094 |
rs186765248 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930309 | GTTTCGCTCTTGTCG[A/C]CCAGGCTGCAATGCA | 26094 |
rs186823426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949198 | TCCCACCGGTAATCT[C/T]AGCATTTTGGGAGGC | 26094 |
rs186907740 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960139 | CTGACTAATACAGCA[C/T]ATTCTATAAAGAACC | 26094 |
rs187196614 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942477 | GACCTTGGAGCAGGG[C/T]CCCTTCAGGGAAGGC | 26094 |
rs187251298 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946692 | CAGGCCGCAGCCAGC[A/C]CTGAGGCTTAAACAA | 26094 |
rs187401331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72935990 | ATGGGGTCTCACTCT[A/G]TTGCCCAGGCTGGTC | 26094 |
rs187419719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955965 | TCTTGCTCTGTCGCC[C/T]GGGCTGGAGTGCAGT | 26094 |
rs187470758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938750 | GGTATATAAGATTTT[C/T]TTTTAAATGGTATAC | 26094 |
rs187564704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939376 | TCTGTAAGATTGTGT[A/G]GTCAAGTAAAATTTA | 26094 |
rs187705240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935059 | GAGATGGGAGTATGA[A/G]CAAACAGTCATGCAG | 26094 |
rs187772833 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925389 | CAAGCTTCATGAAGC[C/G]GTTCTTTATTCTGAC | 26094 |
rs187776989 | snp | C/T | 0.000659674 | 0.0181494 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954113 | GAACCCAGTGGTCCC[C/T]GGCCTGCCTAGAAGG | 26094 |
rs187823343 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959531 | TCAGATTCAAGGGCC[C/T]GGCGTCAAAGGAAAT | 26094 |
rs188018284 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928929 | ATTCTGAGTTTTGGC[C/T]CCGTGCTAAGGCTGG | 26094 |
rs188034046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948803 | AATGGTACTTTGTTC[A/G]GACCTGCACTCTGCA | 26094 |
rs188081701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955171 | TCTCTAGAAAATGCC[A/G]TCTTCCCTTAAAAGT | 26094 |
rs188121958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950479 | AGACTGATGAGAACA[C/T]TTCTCTGGGAAGGTG | 26094 |
rs188180826 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952657 | ATGTGAGGGAGGCCT[C/G]TGGGGTACTGGATTG | 26094 |
rs188352583 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944028 | TGAATGAGTAGAATC[A/G]TCTCTTGTGGTTGGT | 26094 |
rs188402876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935218 | AGCCTTTAAACTCTT[A/G]CTGTATTTGGAAGGC | 26094 |
rs188547918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940737 | CTGGGACTACAGGCA[C/T]GTGCCACCATGCCCA | 26094 |
rs188615234 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961789 | ATACCACACCCAGGG[A/G]AATGGGGAAGCCAAG | 26094 |
rs188616905 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924836 | TTTCTCCCCAACCCC[C/T]TACACGGTGATTTCC | 26094 |
rs188787614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946121 | ACTGGGGAAGAGGGC[A/C]GAGCATACTTACCTC | 26094 |
rs188795806 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926123 | AGCGAGAGGACTTCT[C/G]CAGGGCCGCATCACC | 26094 |
rs188890188 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961110 | CAGGCTGGTCTTGAA[C/T]TCCTAGGCTCAAGTG | 26094 |
rs188952259 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945373 | ACTCCAGCCTGGGTG[A/T]CAACAGTGAGACCCC | 26094 |
rs189158832 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940054 | TGAGGCAAACCGCCT[C/T]CCCCAGGACTGAGCA | 26094 |
rs189193745 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927612 | CGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 26094 |
rs189217066 | snp | C/T | 8.23716e-05 | 0.00641709 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940315 | ACGAAAGAGAGCATC[C/T]GGCAGAAGGAGATGG | 26094 |
rs189256002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947470 | CTTCACATGCATGTG[G/T]TGGAGACAGAATGGG | 26094 |
rs189461876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932606 | CCCAACCTTCTGCAA[C/T]ACACCTGATTTTAAC | 26094 |
rs189463111 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931093 | TTGGGTATTCTGGGT[C/G]CCTTGCATAATATGA | 26094 |
rs189496418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950697 | GAGACACCCACATGT[A/G]GTCAGGGAAATGCAA | 26094 |
rs189497412 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961616 | CATTCACAGTCTTCC[C/T]GCAATTATTCCTGGT | 26094 |
rs189504630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931770 | CAGTGCTTTTTCTGT[A/G]TATCAATTGAGAAAA | 26094 |
rs189555192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939524 | CCTTTTAATCTGGAA[A/G]ATTCCACAAGACCTC | 26094 |
rs189786932 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956941 | GCCCCGGCCCGGCGC[A/G]GTGGCTCACGCCCGT | 26094 |
rs189794258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942704 | CGCACTTTCGTCATC[G/T]CAGGGGAAGGAGCTG | 26094 |
rs189999226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946295 | AGCTGCTTGGGGGCT[C/T]GGGGGGAGGTGAGGT | 26094 |
rs190011677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943183 | AGTCATCAAACCTGG[C/T]TCTGGAGAAGCCAAC | 26094 |
rs190022002 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924556 | AGAGCCTGCTGGCCG[C/G]CTGCCAGCCACTCAT | 26094 |
rs190041374 | snp | C/T | 0.000238574 | 0.0109192 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72937955 | ATGTATGGATTTTTT[C/T]GTTTTTCTCTTTTAG | 26094 |
rs190242275 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936699 | CTTTTGAACCTGTTG[A/G]GTCTGTGGAGATAGA | 26094 |
rs190262148 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928334 | GAGTAGCTGAGACTA[C/T]GGGCGCACGCCACCG | 26094 |
rs190275242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948039 | ACACCTACTTCCTGA[C/G]TTGTGGTGAGATTAA | 26094 |
rs190282513 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927197 | ATGACGCCTTTCACC[A/C]TGGTGTTCTACAGGC | 26094 |
rs190509059 | snp | A/G/T | 0.000129314 | 0.00804004 | missense | DCAF4 | GRCh38.p7 | 14:72956488 | CACGAGGAAGAAGGA[A/G/T]TCCTGGTGGCAGGTA | 26094 |
rs190613260 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959962 | GGCTGTAACCAAAAC[C/G]CACCACTTCTATTGG | 26094 |
rs190656525 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938260 | GGGCATGTCGCTTTG[A/G]TGGGTCAGCCCACCT | 26094 |
rs190794358 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942181 | GAGTTGTCACCAACA[A/G]TGGGGCATTAAGTGG | 26094 |
rs190840342 | snp | C/T | 0.00136719 | 0.0261099 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954307 | AGAGGCCTTAACAGG[C/T]CTTAAAACCCCATGT | 26094 |
rs191107950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933155 | ACCCCTCCTTCTCCC[A/G]AGCTGTGACAAACAA | 26094 |
rs191122328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935198 | AAAGGTACTGTCTTT[A/G]TCCTAGCCTTTAAAC | 26094 |
rs191199848 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953812 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26094 |
rs191248563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940614 | TTTTTTTTTTGAGGC[A/G]GAATCTCACTCTGTT | 26094 |
rs191312737 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961629 | CCCGCAATTATTCCT[A/G]GTGCAGGGTTTTATT | 26094 |
rs191364605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953297 | GAGCCACCACGCCTG[G/T]CATGGATTGTTTTAT | 26094 |
rs191493811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945752 | GTCATCTCCACTCTC[A/G]CTCATGGAGAGGAAC | 26094 |
rs191687276 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948366 | CTTACATTTCAAAGG[A/G]TCATAGAGCCTAAAT | 26094 |
rs191774299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946139 | GCATACTTACCTCAT[C/T]TTTCCATAAGACTTG | 26094 |
rs191886119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936122 | CACTGGCCACACGTG[C/T]TTCCCTTCCTGTGCG | 26094 |
rs191900966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955985 | TGGAGTGCAGTGGTA[C/T]TATCTTGGCTTACTG | 26094 |
rs191914437 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938755 | ATAAGATTTTTTTTT[A/G/T]AATGGTATACCTATG | 26094 |
rs191958611 | snp | A/C | 0.0146728 | 0.0844358 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928511 | GTCTACAGACTCTTA[A/C]AAAATTCCCCTGTTG | 26094 |
rs192151995 | snp | C/G/T | 3.46254e-05 | 0.00416071 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939915 | CAGGTAAGGCCACTT[C/G/T]CGGGGTGGGAATCCT | 26094 |
rs192169595 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960202 | ATACTTGTTGCCCAG[C/G]CTGGAGTGCAATGGC | 26094 |
rs192178077 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930314 | GCTCTTGTCGCCCAG[C/G]CTGCAATGCAGTGGC | 26094 |
rs192189103 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958902 | TTTTAAGTGACACTC[A/C]GTGTACACAGATCCC | 26094 |
rs192450822 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948869 | TTCTTTCTACACTTA[A/T]TGGGCCCTTAGTTAA | 26094 |
rs192461307 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929127 | CCCCGCCCCCCACCC[C/T]GCCCGGCCTCCTCTG | 26094 |
rs192527530 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949426 | ACACTACTGCACTCC[A/G]GCCTGGGTGAAAGAG | 26094 |
rs192696217 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935499 | ACCTCAGGTGATCCA[C/T]CCGCATCGGCCTCCC | 26094 |
rs192818964 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924842 | CCCAACCCCCTACAC[A/G]GTGATTTCCCAGAAG | 26094 |
rs192910770 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926201 | GTTCCGCTGCTCCGG[A/G]AGCAGCCCCCGGCCC | 26094 |
rs192966792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950619 | TCAAAAGACACACAC[A/G]TAGGCAAGGGTATAA | 26094 |
rs193035310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944851 | CCCAGCACTTTGGGA[A/G]GCTGAGATGGGAGGA | 26094 |
rs193096472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940217 | TAATTTTTTTGTCTA[A/G]AGAGCTACCTGGGTT | 26094 |
rs193170981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931523 | TGGTTGCCTTTTCTT[C/T]GTCTTGCCTAATTGC | 26094 |
rs193250448 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961266 | TGGCAAGAAGGGCTG[A/G]GCTGGGATTAAGATT | 26094 |
rs199532651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934612 | CATTTTCATTCTTCA[C/G]ACTGCACTTATCTCC | 26094 |
rs199555282 | snp | A/G | 2.78524e-05 | 0.00373168 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956512 | GCAGGTACTTGAGGA[A/G]GGAAGGGGAAGTTCC | 26094 |
rs199560991 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952712 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTTGCT | 26094 |
rs199575423 | snp | C/T | 0.000285266 | 0.0119395 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939916 | AGGTAAGGCCACTTG[C/T]GGGGTGGGAATCCTG | 26094 |
rs199575616 | snp | A/C | 1.65228e-05 | 0.00287422 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951903 | CTCCTCCTTTAAAGA[A/C]ATCTGTCCTCTGTCT | 26094 |
rs199623989 | in-del | -/AGTTTA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953763 | TATATATATATATAT[-/AGTTTA]TTTATTTATTTATTT | 26094 |
rs199670209 | snp | A/C/G | 0.000132005 | 0.00812322 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958682 | AACCATACCCTCCCC[A/C/G]TACCCTGCCTCCAAG | 26094 |
rs199749299 | snp | A/C/T | 0.0011854 | 0.0243171 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947233 | GGTGGGCAGGCCACA[A/C/T]CCTGACGTTGGACCT | 26094 |
rs199841269 | snp | C/G | 0.0618563 | 0.164627 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962186 | GGTGAGACGAGAAGG[C/G]CTTCTCAGGCCTATG | 26094 |
rs199861571 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952033 | GCATGTGTTTTTTTT[-/A]CAGCATCTGCCCCTT | 26094 |
rs199928850 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937233 | ATGGGGGAACAGATA[G/T]ATGTCTGCAGTTCCT | 26094 |
rs200002099 | snp | A/G | 0.00199792 | 0.0315431 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941782 | CATCTTCCATGCTAC[A/G]AAAAAGCCAGCTGGG | 26094 |
rs200019519 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943065 | GCATGGATCCCTCCG[C/G]CTTGGCAAGCGACCG | 26094 |
rs200035451 | snp | A/G | 4.94923e-05 | 0.0049743 | missense | DCAF4 | GRCh38.p7 | 14:72954413 | GGGTCCTGTTGACCA[A/G]CGTGGTGACGGGACA | 26094 |
rs200055443 | in-del | -/TTCT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931986 | GACCTATATTTTTCC[-/TTCT]TTTTTTTTTTTTTTT | 26094 |
rs200102947 | in-del | -/ACA | 0.0236746 | 0.106192 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928499 | GCGCCCGGCCAGTCT[-/ACA]ACAGACTCTTACAAA | 26094 |
rs200313748 | snp | C/G | 1.65179e-05 | 0.00287379 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946049 | TGCCCATCCCTGTAG[C/G]CTCTCTGCACACTTG | 26094 |
rs200344354 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928121 | AGCTACTTTGTATTC[-/A]GCTTTACAGACCAGT | 26094 |
rs200357907 | in-del | -/AAAT | 0.0670745 | 0.170406 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957212 | CGAGACTCCGTCTCA[-/AAAT]AAATAAATAAATAAA | 26094 |
rs200358217 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935273 | ATGATTTTTTTTTTT[G/T]AGACGGAGTTTCACC | 26094 |
rs200407119 | snp | A/G | 9.88745e-05 | 0.00703047 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943047 | AAAAGGTCCAGATTC[A/G]AAGCATGGATCCCTC | 26094 |
rs200440706 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928187 | TACAGAATCCCCCCA[C/T]TTTTTTTTTTTTTTT | 26094 |
rs200464665 | snp | C/T | 0.00237639 | 0.0343882 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958601 | TGCCATGTGTCTCTC[C/T]TCTTTCCTAGTGGGC | 26094 |
rs200500208 | snp | A/G | 0.00192256 | 0.0309448 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955734 | AGGCCACAGGGTCTC[A/G]TGGCCCAGTGCCCTG | 26094 |
rs200596062 | snp | A/T | 0.170084 | 0.236883 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962514 | CACACACACACACGC[A/T]TGCACACTCTCTCTC | 26094 |
rs200682888 | snp | A/C/G | 3.64128e-05 | 0.00426677 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940420 | TCCTCTCCGCTCCTG[A/C/G]CAGCACCTGTCCATC | 26094 |
rs200764103 | snp | C/T | 0.00225183 | 0.033479 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72937968 | TTTGTTTTTCTCTTT[C/T]AGGAACAGAAATGAA | 26094 |
rs200794162 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953742 | AAAAAAATATATATA[A/T]ATATATATATATATA | 26094 |
rs200860175 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935794 | CTGAAGTCTTTGACT[G/T]ACCAGTTCGTGTGTT | 26094 |
rs200953340 | in-del | -/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928583 | GTGTAGTAAACATCC[-/TT]TTTATATATATATAT | 26094 |
rs200959646 | in-del | -/G | 0.0217236 | 0.101931 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932238 | TCAGGCGATCTGCCT[-/G]CCTTGGCCTCCCAAA | 26094 |
rs200960019 | snp | A/G | | | missense | DCAF4 | GRCh38.p7 | 14:72955572 | AAATCTTTGCCATTG[A/G]TCTGCGTTGTGGAAA | 26094 |
rs201045510 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954275 | CAGGTGAGCCTGGCT[C/T]CCCAGGTGCCCAGAG | 26094 |
rs201167859 | in-del | -/T | 0.0221141 | 0.102801 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938745 | ATAGGGTATATAAGA[-/T]TTTTTTTTTAAATGG | 26094 |
rs201185368 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958588 | TCTCTCACTAGCCTG[C/T]CATGTGTCTCTCCTC | 26094 |
rs201345797 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927343 | AGTCGCGGTGGTGTT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs201392432 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951749 | AAATGTCCATGCCTC[C/T]TCCCAGAGGGGAGCC | 26094 |
rs201480605 | snp | C/T | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962515 | ACACACACACACGCA[C/T]GCACACTCTCTCTCT | 26094 |
rs201510695 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954558 | ATTGAAATTGGACTC[C/T]TCTGTGTGCCATCTA | 26094 |
rs201529208 | snp | C/T | | | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954216 | CCCTGGTGCCTGGTC[C/T]TGTGCCTGGTCCCTG | 26094 |
rs201559584 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937411 | CAATTTTTCTTTTCT[-/TTC]TTTTTTTTTTTTTTT | 26094 |
rs201604003 | snp | A/G | 0.00140536 | 0.0264709 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945843 | GGCAGTCCACCAGGC[A/G]CAGCCTGGGACGTCA | 26094 |
rs201721023 | in-del | -/CGAG | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962178 | GGAGAGGAGGTGAGA[-/CGAG]AAGGGCTTCTCAGGC | 26094 |
rs201738354 | in-del | -/CTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931985 | TGACCTATATTTTTC[-/CTT]CTTTTTTTTTTTTTT | 26094 |
rs201827930 | in-del | -/AGGGGCGGGG | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926651 | AGGAAGGCCAGGGAA[-/AGGGGCGGGG]AGGGGCGGGGAGGAG | 26094 |
rs201937947 | snp | A/G | 8.2373e-05 | 0.00641714 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941808 | CTGGGTTTTCTCAAC[A/G]TCACCAATTACTGCC | 26094 |
rs201948923 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953800 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26094 |
rs201981712 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962512 | CACACACACACACAC[A/G]CATGCACACTCTCTC | 26094 |
rs201996281 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940974 | TAACTGTTTTTTGGG[G/T]TTTTTTTGAGACAGG | 26094 |
rs202043635 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928597 | CCTTTATATATATAT[A/T]TATATATATATATAT | 26094 |
rs202091513 | snp | A/G | 0.00199792 | 0.0315431 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940240 | CCTGGGTTTTACTTT[A/G]ACCCTGAAAAGAAAC | 26094 |
rs202097624 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937232 | TATGGGGGAACAGAT[A/G]GATGTCTGCAGTTCC | 26094 |
rs202156671 | in-del | -/TG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940590 | TCTTGTTCGATAAGT[-/TG]TTTTTTTTTTTTTTT | 26094 |
rs202174615 | snp | A/G | 8.25457e-05 | 0.00642386 | missense | DCAF4 | GRCh38.p7 | 14:72954415 | GTCCTGTTGACCAAC[A/G]TGGTGACGGGACACC | 26094 |
rs367672481 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958681 | GAACCATACCCTCCC[C/T]GTACCCTGCCTCCAA | 26094 |
rs367684354 | snp | A/G | 9.8837e-05 | 0.00702914 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954174 | AGCAGGAATAGACCG[A/G]CCTGGCATGCTCTGC | 26094 |
rs367739807 | snp | C/T | 0.000347939 | 0.0131852 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955471 | ACCTGCCCTGCCCAG[C/T]CTCAGAGGGATGTCA | 26094 |
rs367786650 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930373 | TCCCGGGTTCAAGCG[A/G]TTGTTCTGGCTCAGC | 26094 |
rs367789844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937570 | GGATTACAGGTGCAC[A/G]TTACAACTCCCGGCT | 26094 |
rs367810391 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945709 | TGGCTTTGCCCAGAC[A/G]TGGCTGCACTAAGTT | 26094 |
rs367873358 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955186 | GTCTTCCCTTAAAAG[C/T]GAATGAACCCACTAA | 26094 |
rs367876787 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937202 | AGCTGAGATAAGGAG[-/AAG]GAGACATTAACATAT | 26094 |
rs367888973 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948815 | TTCAGACCTGCACTC[G/T]GCATTTTTCCTGCAA | 26094 |
rs368075846 | snp | A/C/T | 0.000988025 | 0.0222071 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947241 | GGCCACACCCTGACG[A/C/T]TGGACCTGGGTATCT | 26094 |
rs368138672 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939952 | TGCACACAGGGAAGG[C/T]TGAGACCCGTTCCTG | 26094 |
rs368191108 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931263 | CTAAGTACTTTTTCT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs368277798 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952611 | GGTCAGGCTCACAGT[A/G]CCCTTTGGGGAGGTA | 26094 |
rs368348395 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955282 | GCAGGGGGGTGGGGG[A/G]CAGCTCCTAGGACCT | 26094 |
rs368440658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929384 | TACACATACGCTGGG[C/T]ACATACTGGCTCTCT | 26094 |
rs368461746 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72951801 | AGCTTTTTCCAGGCT[A/G]TGCCTCATGGGACTC | 26094 |
rs368550192 | snp | G/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959152 | CTTCTTCCTCCAAGA[G/T]CCCATTGAAGAAGCC | 26094 |
rs368560012 | snp | G/T | 1.65526e-05 | 0.00287681 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942990 | CCACCCTCTGTTTCT[G/T]CAGTTTAGCCCACGA | 26094 |
rs368730949 | snp | C/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924715 | TCCCATCTGTACCCC[C/G]CTTCCATCCTGGCTA | 26094 |
rs368794661 | snp | C/T | 1.67464e-05 | 0.0028936 | synonymous-codon, missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938047 | GCAGAACCCTTGGTT[C/T]AGACTCCGTGATTCT | 26094 |
rs368815833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951629 | AAACAAACAAACAAA[A/C]AAAAAACATCTGAAG | 26094 |
rs368846748 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956270 | GAATTCGAGATGGAG[A/G]TCTTCATGACCTGCA | 26094 |
rs368963532 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956527 | AGGAAGGGGAAGTTC[C/T]ACCCCATCAAATACT | 26094 |
rs369035983 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952848 | CACAGGCGCACACCA[C/T]CACGCCCGGCTAATT | 26094 |
rs369081180 | snp | A/T | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943044 | GGAAAAAGGTCCAGA[A/T]TCGAAGCATGGATCC | 26094 |
rs369082539 | in-del | -/GTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953764 | ATATATATATATATA[-/GTTT]ATTTATTTATTTATT | 26094 |
rs369242327 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939468 | GTGCTGACAAATGAG[C/G]CCAGCTGGTAAAATT | 26094 |
rs369255127 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953332 | TAACCTGGGTGGTGG[A/G]TACATGGCTATATTT | 26094 |
rs369306012 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962180 | AGAGGAGGTGAGACG[A/G]GAAGGGCTTCTCAGG | 26094 |
rs369307572 | snp | A/G | | | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945932 | AACGATGTTAAAGTT[A/G]GAGGCTCCAAGTATG | 26094 |
rs369368866 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951117 | TCCCAAGGAGCTGGT[A/G]CTACAGGCACACACC | 26094 |
rs369457969 | snp | C/T | 0.447032 | 0.153878 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937410 | GGCAATTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs369465433 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960287 | CCCGAGTAGGTTGGA[C/T]TATAGGCGCGTGCCA | 26094 |
rs369505774 | snp | A/G | 1.73519e-05 | 0.00294545 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938106 | AGCCACTTTTGCCCA[A/G]TGTGCTTCTGGCATT | 26094 |
rs369765405 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931737 | TTTTTTAATCATGAG[A/C]GGATGTTGCATTTTG | 26094 |
rs369830006 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932092 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 26094 |
rs369863799 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953736 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 26094 |
rs369915708 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943617 | CTTCTCTGGTTTGGG[G/T]TGGACCCAAGCTGGA | 26094 |
rs369961388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952944 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 26094 |
rs369999328 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946562 | TCCAGGGGTCCAGGA[A/G]TTGATCTGGAAGGGC | 26094 |
rs370016560 | snp | A/G/T | 4.94184e-05 | 0.00497063 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940256 | ACCCTGAAAAGAAAC[A/G/T]CTACTTCCGCTTGCT | 26094 |
rs370072783 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932884 | GAATAATTTTTTTTT[C/T]TTTCTTTCTTTCTTT | 26094 |
rs370127536 | in-del | -/T/TT/TTT | 0.499998 | 0.000998401 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931263 | TAAGTACTTTTTCTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 26094 |
rs370177630 | snp | A/G | 0.000179966 | 0.00948423 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958773 | CTGCTCATGGCTGTC[A/G]GGCAGGACCTTTACT | 26094 |
rs370247731 | snp | A/G | 0.000115425 | 0.00759599 | missense | DCAF4 | GRCh38.p7 | 14:72954431 | TGGTGACGGGACACC[A/G]GCAGTCCTTTGGGAC | 26094 |
rs370328980 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72947153 | CCAGGTGAATTCGGT[G/T]TGCTGGGCCTCGCTG | 26094 |
rs370354470 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954948 | GGTGAAACCCCTTCT[C/T]TACTAAAAATACGAA | 26094 |
rs370561305 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944477 | TAACCACATCATGTT[C/T]TAAAATGAGAAAAGA | 26094 |
rs370570965 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940733 | GTAGCTGGGACTACA[G/T]GCACGTGCCACCATG | 26094 |
rs370658460 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958954 | AAGTGCTGAATGTTC[C/T]GTGTGGAGATGCTCA | 26094 |
rs370663818 | in-del | -/CTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932900 | TTTCTTTCTTTCTTT[-/CTTT]TTTTTAATGTTGTTT | 26094 |
rs370730294 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929726 | GATGAACTTGAGGGC[C/G]CATTTCTCCTTGAAG | 26094 |
rs370732462 | snp | C/T | 1.71593e-05 | 0.00292905 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955498 | GTCATGATAGCCAGG[C/T]ACTGAGCAGTCCCTC | 26094 |
rs370767404 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933591 | TCTCTAATTCTCACT[A/G]TATACCATTACCACT | 26094 |
rs370853099 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936536 | GCCACTGCACTCCAG[C/G]CTGGGCAACAGAGCG | 26094 |
rs370863403 | snp | G/T | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926862 | AGACCTGCTGCTGAA[G/T]GCCCCACCCGACACC | 26094 |
rs370871598 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951441 | ACTTGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 26094 |
rs370917826 | snp | A/C | 0.00116094 | 0.0240649 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939855 | GCCACGGTGATGACG[A/C]GTCTCCGTCAACCTC | 26094 |
rs370953411 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929459 | GTCATCCCAACGCTG[C/T]GCCAAGGCAGGAGGA | 26094 |
rs370983187 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948097 | AGCAGTTTCTGGACA[C/T]CATTGGTCCTCGACA | 26094 |
rs371021855 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962184 | GAGGTGAGACGAGAA[A/G]GGCTTCTCAGGCCTA | 26094 |
rs371027284 | snp | A/G | 6.59554e-05 | 0.00574224 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958650 | ATCTGGAGCCTCCAC[A/G]ATGCCCGCCTACTGA | 26094 |
rs371098154 | snp | A/G | 8.24273e-05 | 0.00641926 | missense | DCAF4 | GRCh38.p7 | 14:72955647 | CAGTGACCTCTGTGC[A/G]GATCCTCCAAGATGA | 26094 |
rs371109570 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935274 | TGATTTTTTTTTTTG[A/T]GACGGAGTTTCACCC | 26094 |
rs371134763 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[-/A]TATATATATATATAT | 26094 |
rs371207694 | in-del | -/TTCTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927341 | AGAGTCGCGGTGGTG[-/TTCTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs371269929 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956547 | CATCAAATACTGTCT[C/T]TCAGGGGCGATCCCA | 26094 |
rs371403617 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954237 | CTGGTCCCTGAATAT[C/T]CAAGCAAATAACTGC | 26094 |
rs371463607 | snp | C/G | 1.65304e-05 | 0.00287488 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958699 | ACCCTGCCTCCAAGG[C/G]CGACATTCCCAGTGT | 26094 |
rs371512823 | snp | C/T | 6.59663e-05 | 0.00574272 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943010 | TTAGCCCACGAGCTG[C/T]GTCTCAGCTGCATGG | 26094 |
rs371553106 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924509 | AGGTATATCTCATGC[C/T]CACGTCACTGTCCCC | 26094 |
rs371555128 | snp | A/G | 3.29484e-05 | 0.00405871 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947240 | AGGCCACACCCTGAC[A/G]TTGGACCTGGGTATC | 26094 |
rs371574557 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930711 | TGCCTAATCAAGATC[A/T]TGATGATTTATACCT | 26094 |
rs371607121 | snp | A/C | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960067 | CACTGTTGCTGGCCC[A/C]GAATGCCTCACTAGG | 26094 |
rs371884296 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960294 | AGGTTGGATTATAGG[C/T]GCGTGCCACCACGCC | 26094 |
rs371995251 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961979 | TCTTTGGAGAGGTCA[C/T]CCACTTCCCTCTGTT | 26094 |
rs372473378 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935657 | GGGGTGAACACATGC[A/T]CTCCCTGGCCCAAAT | 26094 |
rs372503421 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929108 | CCCTACTGGGTGTAG[C/G]GCACCCCGCCCCCCA | 26094 |
rs372535405 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933067 | GCTGAAGAATGTGTG[C/G]AAGCTGCCCTGCGCA | 26094 |
rs372573738 | snp | C/T | 5.52573e-05 | 0.005256 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958795 | ACCTTTACTGTTACT[C/T]CTACAGCTAATTCTG | 26094 |
rs372612396 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931265 | AAGTACTTTTTCTCT[C/T]TTTTTTTTTTTTTTT | 26094 |
rs372621310 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947595 | CGGAGGGCTGGTGTG[A/G]TAGCAGAGGAACAAG | 26094 |
rs372669697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929797 | AGCCACACACCTCCC[A/G]GATCATGTCCCGCTA | 26094 |
rs372672880 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | DCAF4 | GRCh38.p7 | 14:72951817 | TGCCTCATGGGACTC[G/T]CAGAGACTCCAGGCT | 26094 |
rs372722916 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949954 | CTGCATGCAGGAGGG[A/G]TTGCAGCCACCTTCC | 26094 |
rs372745291 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927572 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 26094 |
rs372750585 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953763 | TATATATATATATAT[A/G]GTTTATTTATTTATT | 26094 |
rs372788094 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944431 | ATACAAAACACATAA[A/C]TATGTGGAGTTTTTG | 26094 |
rs372813379 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940723 | AGCCTCCTGAGTAGC[C/T]GGGACTACAGGCACG | 26094 |
rs372838478 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938865 | TACTGTATGCTAGTG[A/T]AGACTTTAAAACCCT | 26094 |
rs372993770 | in-del | -/GGCAGCCGTATCCTGGGGCTCTTCCC | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942626 | CCTGGGGCTCTTCCC[-/GGCAGCCGTATCCTGGGGCTCTTCCC]AGCAGCGGAGTGCCC | 26094 |
rs373000336 | snp | A/G | 0.000106805 | 0.00730693 | missense | DCAF4 | GRCh38.p7 | 14:72956431 | TGCGTAAGGCAGTAC[A/G]AAGGCCACGTGAATG | 26094 |
rs373029458 | snp | A/G | 2.89164e-05 | 0.00380228 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939778 | AGTCCTGGGCTGCAA[A/G]TTAACACAGCTGTGT | 26094 |
rs373042856 | snp | C/T | 0.000115366 | 0.00759405 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954380 | GCCCATCTCTGTCTC[C/T]GCCAGGCTTGTCTCG | 26094 |
rs373044182 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949800 | AGAAGATTTTTAAAA[-/A]GTTACATGATTGCTT | 26094 |
rs373046291 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950858 | TTATTGACAAATATA[A/T]GTAGTGGAAATACAG | 26094 |
rs373154341 | snp | A/C/G | 4.94192e-05 | 0.00497067 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945928 | AGTGAACGATGTTAA[A/C/G]GTTGGAGGCTCCAAG | 26094 |
rs373244735 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962181 | GAGGAGGTGAGACGA[A/G]AAGGGCTTCTCAGGC | 26094 |
rs373255158 | snp | C/T | 0.000153988 | 0.00877328 | missense, synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938051 | AACCCTTGGTTCAGA[C/T]TCCGTGATTCTGAAG | 26094 |
rs373280904 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928800 | GGTTGTTGGGCTCCA[A/G]TCCAGGCCCCCTAAC | 26094 |
rs373379605 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946227 | GAAACCTTGTCTCTA[-/C]AAAAAAAAAAAAAAA | 26094 |
rs373409844 | snp | A/C/G | 0.000132089 | 0.0081259 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954396 | GCCAGGCTTGTCTCG[A/C/G]CGGGTCCTGTTGACC | 26094 |
rs373422333 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936137 | CTTCCCTTCCTGTGC[A/G]CAGTCCCTTTCAGCT | 26094 |
rs373470081 | in-del | -/ATATATATATAG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928607 | TATATATATATATAT[-/ATATATATATAG]TTCACATACCCTAAA | 26094 |
rs373499981 | in-del | -/TGGGGGCT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946287 | GTAGTCCCAGCTGCT[-/TGGGGGCT]CGGGGGGAGGTGAGG | 26094 |
rs373645931 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930044 | GTTGAGGCAGGAGGA[A/C]GGCTTGAGCCGGGGA | 26094 |
rs373669917 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945591 | TAGGGCTCTCCCAAA[C/T]CCACTTCTGAGTGAG | 26094 |
rs373686583 | in-del | -/CCAGTACCCTG | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960116 | CTTGAATGTTTCCTG[-/CCAGTACCCTG]ACTAATACAGCATAT | 26094 |
rs373722073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948748 | GCTGAAGATTTTTTG[G/T]GCTGCTTCAGAAGTT | 26094 |
rs373734829 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947252 | GACGTTGGACCTGGG[C/T]ATCTGTGGGCTTCAT | 26094 |
rs373770788 | snp | C/T | 0.000181328 | 0.00952004 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940345 | GAGAGCAAGAGACTG[C/T]GGCTGCTCCAGGAAG | 26094 |
rs373789802 | in-del | -/ATATATATATA | 0.473266 | 0.112482 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928589 | GTAAACATCCTTTAT[-/ATATATATATA]TATATATATATATAT | 26094 |
rs373882499 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928455 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 26094 |
rs373909613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957700 | GTAATAAACTGCAGC[C/T]GGGATTCAGCTTCAG | 26094 |
rs374019443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928686 | TTTATTATTATATTG[G/T]CAAGATTGTGCAACC | 26094 |
rs374118961 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925283 | GAGTTTTCCTTCCAA[A/G]ACTCCCCTCCCATCC | 26094 |
rs374160459 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943832 | GGAGCATCTGGACTC[A/G]GTCATCTGCTGGTGG | 26094 |
rs374195436 | snp | C/G | 1.65633e-05 | 0.00287774 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958585 | CATTCTCTCACTAGC[C/G]TGCCATGTGTCTCTC | 26094 |
rs374265385 | snp | C/T | 1.71979e-05 | 0.00293235 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958743 | CGGCTGGGGGGCTCC[C/T]GGGGCGCGCCGGGGC | 26094 |
rs374280024 | snp | A/G | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926904 | GGGCTGCGGGCCTTG[A/G]GGCGGTGTCCCCTGT | 26094 |
rs374337546 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956058 | CTCCTGAGTAGCTGG[A/G]ATTACAGGTACCCGC | 26094 |
rs374358720 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954988 | GGCATAGTGCTGGGC[A/G]CCTGTAATCCCAGCT | 26094 |
rs374579479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932191 | ATGAGGTTTCACTCT[A/G]TGTTGGCCAGGCTGG | 26094 |
rs374600927 | in-del | -/TTCTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927341 | AGAGTCGCGGTGGTG[-/TTCTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs374603148 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934210 | CAAGGCTGGAGTGCA[A/G]TGGCGCTATCTCGGC | 26094 |
rs374713201 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951516 | CTCAGGAAGCCGAGG[C/T]AGGAGAATCGCTTGA | 26094 |
rs374771295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947245 | ACACCCTGACGTTGG[A/G]CCTGGGTATCTGTGG | 26094 |
rs374834364 | in-del | -/A | 0.0442548 | 0.142017 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945396 | AGACCCCACCTCTTA[-/A]AAAAAAAATAGCCTA | 26094 |
rs374867813 | snp | A/C | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926797 | CGTAAACACGCAGGG[A/C]GGGCACCCCGAGTGT | 26094 |
rs374904080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934299 | GTGGGGATTGCAGGC[A/G]CCCACTACCATGCCT | 26094 |
rs374994547 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927333 | TGGAAATTAGAGTCG[C/T]GGTGGTGTTCTTTTT | 26094 |
rs375042258 | snp | C/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925928 | CAGCAAGCAGCAGTA[C/G]TGGAGCCAACACGGA | 26094 |
rs375045899 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939092 | GGTGTGGTGGCTGAC[A/G]CCTGTAATCCCAGCA | 26094 |
rs375118905 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951625 | CAAAAACAAACAAAC[-/A]AAAAAAAAAACATCT | 26094 |
rs375138420 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943533 | AGGACTCCTTGCTTG[C/G]CGCCCCTGGCTTCAG | 26094 |
rs375141277 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957471 | GGTATTCCTATAGAA[A/C]GGGCTTATACCCCAT | 26094 |
rs375328405 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946387 | TCCAACCTGGGTAAC[-/AG]AGCGAGACCCTGTCT | 26094 |
rs375396587 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948076 | TTAACTCCTGTGAAG[C/G]CACCTAGCAGTTTCT | 26094 |
rs375504883 | snp | C/T | 0.000153988 | 0.00877328 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939873 | CTCCGTCAACCTCGT[C/T]TGGCACAGCTGGGAC | 26094 |
rs375554291 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927413 | CTGGAGTGCAGTGGC[A/G]CGATCTCGACTCACT | 26094 |
rs375567777 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937405 | TGCCTGGCAATTTTT[C/T]TTTTCTTTTTTTTTT | 26094 |
rs375598356 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946296 | GCTGCTTGGGGGCTC[A/G]GGGGGAGGTGAGGTG | 26094 |
rs375602879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931453 | TGAATTCATTTGTGA[A/G]GTCCAGTAGATTTTT | 26094 |
rs375854555 | snp | C/T | 1.71684e-05 | 0.00292983 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958748 | GGGGGGCTCCCGGGG[C/T]GCGCCGGGGCTGCTC | 26094 |
rs375967391 | snp | A/G | 0.00010255 | 0.00715992 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942962 | ATGGATGTCAGCTTC[A/G]GCATCCATGCCCCCA | 26094 |
rs375989976 | snp | A/C/G/T | 0.00125195 | 0.0249899 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954297 | TGCCCAGAGAAGAGG[A/C/G/T]CTTAACAGGCCTTAA | 26094 |
rs376179404 | in-del | -/CTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931988 | CCTATATTTTTCCTT[-/CTTT]TTTTTTTTTTTTTGA | 26094 |
rs376184952 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960882 | CAGGCCCCCCCCACC[-/T]TTTTTTTTTTTTTGA | 26094 |
rs376261628 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953881 | TAGGTGATCGAGGAT[C/T]GGAGCCACCTTACCT | 26094 |
rs376344693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951567 | GGTAAGCCGAGATCG[C/T]GCCATTGCACCCCAG | 26094 |
rs376362503 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945981 | GTCTGAAGACCCCTA[C/T]GCTCAAGGTGTTCAT | 26094 |
rs376365595 | in-del | -/TAGTTGG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946075 | ACTTGACCCTGGGGG[-/TAGTTGG]CCAAATTCAGGGTAG | 26094 |
rs376389911 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928270 | GCGATCTCGGCTCAC[C/G]GCAACCTCCGCCTCC | 26094 |
rs376438613 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928962 | CGACCCCCTGTGCTG[A/T]CAAGCCTACCTCCCA | 26094 |
rs376438962 | snp | A/G | 3.29951e-05 | 0.00406159 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940181 | AGGTGGTCAGTTCAC[A/G]GTGGTTGAAATTGGT | 26094 |
rs376538808 | in-del | -/TATATAT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953734 | AAAAAAAAAAAAAAA[-/TATATAT]ATATATATATATATA | 26094 |
rs376550366 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937945 | ACACACAGAGATGTA[C/T]GGATTTTTTTGTTTT | 26094 |
rs376643226 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943024 | GCGTCTCAGCTGCAT[A/G]GAGAGGAAAAAGGTC | 26094 |
rs376776226 | snp | A/C | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962489 | ACCCTGTCTTTACAA[A/C]ACACACACACACACA | 26094 |
rs376906322 | in-del | -/TGTGTGTGTG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953783 | ATTTATTTATTTATT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 26094 |
rs376943869 | snp | A/C/G | 6.58896e-05 | 0.00573943 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72947150 | TCACCAGGTGAATTC[A/C/G]GTGTGCTGGGCCTCG | 26094 |
rs376971781 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962179 | GAGAGGAGGTGAGAC[A/G]AGAAGGGCTTCTCAG | 26094 |
rs377030472 | snp | C/G | 7.47873e-05 | 0.00611458 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958825 | GCAGGGCACAGCCCA[C/G]AGCCATGTGGATTTG | 26094 |
rs377073321 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954430 | GTGGTGACGGGACAC[A/C]GGCAGTCCTTTGGGA | 26094 |
rs377123285 | snp | A/C | 1.66938e-05 | 0.00288905 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954514 | ACAGGCAGAATATAA[A/C]AGTTTGCCCCATGTA | 26094 |
rs377142284 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944630 | AAACCCCGTCTCTAC[A/C]AAAAAATATAAATTA | 26094 |
rs377283181 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940728 | CCTGAGTAGCTGGGA[C/T]TACAGGCACGTGCCA | 26094 |
rs377286626 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953930 | CCTGATATCAGTACT[A/G]TTCGTACTGTAAACA | 26094 |
rs377287966 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931988 | CCTATATTTTTCCTT[-/C]TTTTTTTTTTTTTTT | 26094 |
rs377298319 | snp | G/T | 1.65094e-05 | 0.00287305 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951884 | GTCACCCAGGTACAG[G/T]GTTCTCCTCCTTTAA | 26094 |
rs377302647 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927569 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGACC | 26094 |
rs377306454 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943475 | TGGGGCAGGACTTGG[C/T]GGCTAAACCTGCAGC | 26094 |
rs377316029 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950184 | TCCTTTGGTGGCATT[G/T]TTGGGGGATAGACGG | 26094 |
rs377316390 | in-del | -/TAAA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957227 | AAATAAATAAATAAA[-/TAAA]AAAGATTTGTGGCCC | 26094 |
rs377369612 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947057 | TGAAGAGAGAAGTCA[C/T]ACGTCTGTGTCCCCA | 26094 |
rs377450299 | snp | C/T | 4.94694e-05 | 0.00497316 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958649 | AATCTGGAGCCTCCA[C/T]GATGCCCGCCTACTG | 26094 |
rs377557451 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934146 | CCCCCACTGCCTTAC[A/G]TGGCATTTTCTTTTT | 26094 |
rs386381752 | in-del | -/AT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930653 | GTGTATATATATATA[-/AT]TGTAGTGTGTGTGAG | 26094 |
rs386778759 | multinucleotide-polymorphism | GG/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948187 | CAAAGGAGTTTTTTT[GG/TT]ATTTTAATTTTTTTC | 26094 |
rs397712115 | in-del | -/AA | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930258 | AAAAAACTCCGTCTC[-/AA]AAAAAAAAAAAAGAA | 26094 |
rs397740506 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940981 | TTTTGGGGTTTTTTT[-/T]GAGACAGGGTCCCAC | 26094 |
rs397747981 | in-del | -/AT | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930654 | TGTATATATATATAT[-/AT]GTAGTGTGTGTGAGT | 26094 |
rs397773608 | in-del | -/TTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935272 | ATGATTTTTTTTTTT[-/TTT]GAGACGGAGTTTCAC | 26094 |
rs397777337 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936579 | AAAAAAAAAAAAAAA[-/A]TACACACACATTTGG | 26094 |
rs397823578 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928981 | CCTACCTCCCAGGGG[-/G]AGGCGAGGCCAGCCC | 26094 |
rs397839940 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952032 | AGCATGTGTTTTTTT[-/T]ACAGCATCTGCCCCT | 26094 |
rs397951620 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941616 | CACCGTCAGATTTTT[-/T]ATGCATATAATTTCT | 26094 |
rs397969375 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941662 | TTTCCTTCATTACAT[-/T]CCTATGGAACTAAAA | 26094 |
rs398025612 | in-del | -/A | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955940 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 26094 |
rs398099457 | in-del | -/A | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962183 | GAGGTGAGACGAGAA[-/A]GGGCTTCTCAGGCCT | 26094 |
rs527236472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938170 | GAGATCACCTGGGGG[C/T]TCGTCCCAATGCAGG | 26094 |
rs527303218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937766 | ATGTGGTCGACTAAG[C/G]GTAACAGGAAGGAAG | 26094 |
rs527432665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938633 | GTAGCCAATTGCTCC[A/G]AGGCTGCAAACCTGT | 26094 |
rs527639550 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941484 | CGCACCTGGTGGCTT[C/T]GTCCCCCCGGGTGTA | 26094 |
rs527668536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951606 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAACAAAC | 26094 |
rs527681066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951114 | GCCTCCCAAGGAGCT[A/G]GTACTACAGGCACAC | 26094 |
rs527753878 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933154 | TACCCCTCCTTCTCC[C/G/T]GAGCTGTGACAAACA | 26094 |
rs527764524 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960243 | CACCCTCCACCTCCT[G/T]GGTTCTAGTGATTCT | 26094 |
rs527795649 | in-del | -/AAGAT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939558 | AAATGCGCGAGTGAG[-/AAGAT]AAGAAGAGGGAATCA | 26094 |
rs527810065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945707 | GCTGGCTTTGCCCAG[A/G]CATGGCTGCACTAAG | 26094 |
rs527837003 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940022 | GAAGGAGCTGGGTGC[A/G/T]TCAGGAATGGTGGTC | 26094 |
rs527904026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939567 | AGTGAGAAGATAAGA[A/G]GAGGGAATCACTGTG | 26094 |
rs527969038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926845 | CTCTAAGCGCTTCTC[G/T]GAGACCTGCTGCTGA | 26094 |
rs528069895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954892 | GAGGCCAAGATGGGT[A/G]GATCACAAGGTCAGG | 26094 |
rs528078071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947610 | GTAGCAGAGGAACAA[A/G]GCAGAAAGGAGCAGC | 26094 |
rs528092555 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961422 | CAGCCCAACTCCACC[A/C/G]TCCTGGGCCACTCCT | 26094 |
rs528201488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948108 | GACATCATTGGTCCT[C/T]GACAAATGATAACTG | 26094 |
rs528287581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948660 | ATTGGACTTAAAGGG[A/G]TGGATGGTCTGTTGT | 26094 |
rs528288877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942418 | CTGTACATGCTCAAG[C/T]GAAGAACCTGCATTT | 26094 |
rs528425767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936665 | GCAGATCGGGGGTTA[A/G]AGAGAAATCATGAAC | 26094 |
rs528434947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929041 | TTGGCTCCGGGGCTG[A/G]TCGGTGTTGGGCGTC | 26094 |
rs528453115 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72962095 | AAAAAATTTGTGTCT[C/T]CAAGTGTGCCGTTTC | 26094 |
rs528558424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955879 | TGAGCCTAATCTGAC[A/G]TAAACAAAAGTGAAA | 26094 |
rs528648584 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934342 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 26094 |
rs528685441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949530 | GAGGCTGAGGCAGGC[A/G]GATCACTTGAGGTCA | 26094 |
rs528796517 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955140 | ATTGTGGTCATTACT[A/G]TATTTCACAGACTTT | 26094 |
rs528813092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943732 | CTTTCGATGGACCAC[A/G]TAAGAGCAGGGCCTG | 26094 |
rs528824798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950330 | CCGGGCATCTTGTGA[C/T]AGGAGAAGGCCAGGA | 26094 |
rs529027467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926776 | CGGCCGGATCAGTGC[C/T]GCAACCGTAAACACG | 26094 |
rs529105235 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937129 | TTTCAGAATATGCCC[A/G]TTTTTTTGGATTAGA | 26094 |
rs529214196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946216 | ACATGCATGGTGAAA[C/G]CTTGTCTCTACAAAA | 26094 |
rs529216485 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945239 | CTCTACAAAAAAATA[A/T]AAAAGTAGCCAGGCA | 26094 |
rs529224793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940571 | CCTTCTTCCATCCCC[A/G]TTTTCTTGTTCGATA | 26094 |
rs529286451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946931 | ATGCCAGATAGACCA[A/G]ATGTCTCCCTGTGGG | 26094 |
rs529303867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940209 | GGTGCATTTAATTTT[A/T]TTGTCTAAAGAGCTA | 26094 |
rs529408877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928312 | GATTCTCCTGCTTCA[C/G]CCTCCCGAGTAGCTG | 26094 |
rs529528024 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72960708 | AGAGACAGGCAAGTG[C/T]TGCCTCCATTTCCAG | 26094 |
rs529692176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943535 | GACTCCTTGCTTGCC[A/G]CCCCTGGCTTCAGTG | 26094 |
rs529800148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930827 | AATTCATTCTTTTGC[A/T]GTTTGATATTCAAAT | 26094 |
rs529863052 | snp | A/C/G | 3.47169e-05 | 0.00416623 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938108 | CCACTTTTGCCCAGT[A/C/G]TGCTTCTGGCATTGT | 26094 |
rs529867370 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943941 | CCCTTCCATGTAAGG[A/G]GTGTTGGGGACCGGG | 26094 |
rs530020276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957927 | TAGGAACTGAAGCAT[G/T]AAACCAGAAAGAGCT | 26094 |
rs530031887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950595 | GGAAAAGGAGAGGAA[C/G]CGCGTCAGTCAAAAG | 26094 |
rs530040793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957231 | AAATAAATAAATAAA[A/T]AAGATTTGTGGCCCC | 26094 |
rs530181831 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950983 | TTTTTGGGCTTTTTA[A/G]TAGTATTTTATTTTT | 26094 |
rs530316148 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939283 | ACTTGTGGATTTACA[A/G]ATCAAGTGTTTTAGC | 26094 |
rs530452152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939540 | ATTCCACAAGACCTC[A/G]CAAAATGCGCGAGTG | 26094 |
rs530467515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960213 | CCAGGCTGGAGTGCA[A/G]TGGCGCTCTCACCGC | 26094 |
rs530492427 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954283 | CCTGGCTCCCCAGGT[A/G]CCCAGAGAAGAGGCC | 26094 |
rs530614951 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931204 | CAACAGTGTTTTATA[C/G]TTTTCTGTGTACACG | 26094 |
rs530724048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941493 | TGGCTTCGTCCCCCC[A/G]GGTGTATGTGGATGG | 26094 |
rs530771858 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928971 | GTGCTGTCAAGCCTA[C/T]CTCCCAGGGGAGGCG | 26094 |
rs531061094 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928627 | TATATAGTTCACATA[A/C]CCTAAAATTAACTTT | 26094 |
rs531080701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929312 | ACTGTGAGAGAGAGC[C/T]GACCTCCTCATGCAT | 26094 |
rs531081889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948894 | AGTTAACCTGTGGCC[A/T]GTCAAAGGATTAAAT | 26094 |
rs531111685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955833 | CCAAGTGATTTGTAG[C/G]CCCTGCATGGGGACT | 26094 |
rs531199836 | snp | C/G/T | 5.53289e-05 | 0.00525946 | missense | DCAF4 | GRCh38.p7 | 14:72956462 | AGTACGCCTACCTGC[C/G/T]CCTGCATGTGCACGA | 26094 |
rs531243201 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951144 | CACCACCACGCCCAG[A/C]TAGTTTTTGTATTTT | 26094 |
rs531294788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932071 | TCGGCTCACTGCAAC[C/T]TCTGCCTCCCAGGTT | 26094 |
rs531311288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937662 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 26094 |
rs531351454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932969 | GTCTTGAACTCCTAG[G/T]CTCAAGCAATCCTCC | 26094 |
rs531488082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948265 | CAATCATAGCTCACT[C/T]CAGCCTAGAACTCCT | 26094 |
rs531520450 | snp | C/T | 3.34594e-05 | 0.00409006 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958723 | CCAGTGTGGCCTTCT[C/T]GTCGCGGCTGGGGGG | 26094 |
rs531609804 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959219 | GCCTGGGTAGCAGGA[A/C]GAAAGACCTGCATCC | 26094 |
rs531619735 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952221 | TTAACAGTCTGCCTA[A/C/T]GTTAAGGCAATTTGA | 26094 |
rs531809686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940539 | AAGAAGACAAGAATA[A/C]GAACAGCCAAGAGCC | 26094 |