SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs531991108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948159 | ATTTTATTTGTTTCA[C/T]AGCACTGTATTTCAA | 26094 |
rs532381874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940157 | GACAGGCCACTGGGC[A/G]CCCAACTCAGGTGGT | 26094 |
rs532390275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956679 | TATATTAGTAATCAG[A/G]AGTGTAAATAAATGT | 26094 |
rs532417610 | snp | A/T | 0.00159617 | 0.0282053 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962522 | CACACGCATGCACAC[A/T]CTCTCTCTTAGCCCA | 26094 |
rs532459431 | in-del | -/CT | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960910 | TGAGACATGGTCTCA[-/CT]CTGTCGCCCAAGCTG | 26094 |
rs532610686 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957193 | CTCCAGCCTGGCAAC[A/T]GAGCGAGACTCCGTC | 26094 |
rs532713740 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937097 | GAAGACATTGAATTC[A/G]TAGATGTAGACCATT | 26094 |
rs532747800 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930385 | GCGATTGTTCTGGCT[C/T]AGCCTCCCAAATAGC | 26094 |
rs532748354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944125 | TCTGGTGATGCACAG[A/G]CCACTGTTCACAAGC | 26094 |
rs532891045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938247 | TAACGTGCTCCCAGG[G/T]CATGTCGCTTTGGTG | 26094 |
rs532917932 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959376 | CCGGGATTCTGCTGT[A/T]ATTATCCAAAGGCGT | 26094 |
rs533140419 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | DCAF4 | GRCh38.p7 | 14:72954196 | ATGCTCTGCAGTTTC[C/T]GGATCCCTGGTGCCT | 26094 |
rs533285696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940633 | TCTCACTCTGTTGCC[C/G]AGGCTGGAGTACAGT | 26094 |
rs533341732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941417 | GCCCTGGGTCACCAC[A/G]GGTGGAATGGAGAGT | 26094 |
rs533350399 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961506 | TTTTTTCCACATGGG[C/T]CAGAGACAAGGGTGA | 26094 |
rs533432293 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955075 | AAGATCACACCACTG[A/C]ACTCCAGCCTGGGCA | 26094 |
rs533445619 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928777 | GGGTGCCCCAGTCTC[A/T]GAGCCCCGGTTGTTG | 26094 |
rs533498076 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930429 | GCCCGCCACCACACC[A/G]AGCTGATTTTTGTAT | 26094 |
rs533509004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935863 | TTAGAATCATTTCAT[A/G]TACAGAATATGCACT | 26094 |
rs533559530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929765 | TGACTCCATGGCGCG[C/T]AGCTCGTACGAAGCG | 26094 |
rs533673613 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962242 | TCTACCCTGCCAGTG[A/G]GATAAGAAGGAGCCA | 26094 |
rs533726479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957409 | GAAATAGTAGCTGCT[A/G]ACACTGCAGAATGTG | 26094 |
rs533812399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943933 | CAGCAGGGCCCTTCC[A/G]TGTAAGGGGTGTTGG | 26094 |
rs533925818 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944971 | GTGCGCACCTGTAGT[A/C]CCAGCTACTCAGGAG | 26094 |
rs533935917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944379 | TTTCACCAAAACCAA[C/T]GTCCAAACTCGTGTG | 26094 |
rs534033278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956940 | GGCCCCGGCCCGGCG[C/T]GGTGGCTCACGCCCG | 26094 |
rs534144922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932299 | CCCGGCCTTGACCTA[C/T]ATTTTTCTTCCTATA | 26094 |
rs534386862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949134 | GGTATGTCACATACA[C/T]ATCACATACTCAGAT | 26094 |
rs534411681 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925257 | GTCACCAAGCCCCAA[A/C]CCACCCTGCTGAGTT | 26094 |
rs534438126 | snp | C/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959157 | TCCTCCAAGAGCCCA[C/T]TGAAGAAGCCCAGTG | 26094 |
rs534539535 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926350 | AGATCGTCCCTATTG[A/G]CGTCGACAGACAGAA | 26094 |
rs534565304 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960997 | GGCTTGAGCAATCCT[C/T]CCACCTCAGTCTTCT | 26094 |
rs534617720 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955853 | GCATGGGGACTGCTT[C/T]GTTGACCATATGAGC | 26094 |
rs534718658 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926179 | CTCACGAAAGGGTCT[C/G]CAGACAGTTCCGCTG | 26094 |
rs534827728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935483 | TGATCTCAAACTCCT[C/G]ACCTCAGGTGATCCA | 26094 |
rs534899111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936311 | GCCCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 26094 |
rs535058388 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961617 | ATTCACAGTCTTCCC[A/G]CAATTATTCCTGGTG | 26094 |
rs535129318 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949732 | ACTGCACTCCAGCCT[A/G]AGCGAAAGAGCAAGA | 26094 |
rs535129720 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925966 | CGGTTTCACGGTCAG[A/G]GCTCGCTACGCTACA | 26094 |
rs535231576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949083 | AGCACCTGGTATATC[A/C]TGGAGATACTTAATT | 26094 |
rs535358809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936963 | CACATGTTGCAGGAA[G/T]AAGGGCTAAAAAGAG | 26094 |
rs535409114 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934218 | GAGTGCAATGGCGCT[A/G]TCTCGGCTCACGGCA | 26094 |
rs535469681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933254 | AACTGTGATGCATAC[C/T]GGGTTTTATATTATT | 26094 |
rs535485281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957677 | GATGCAGGTAGTTAC[C/T]AGCTGCAGTAATAAA | 26094 |
rs535510889 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951295 | GCTTTTAACTATATC[C/T]GATTTGTTTTTCCCT | 26094 |
rs535591478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72926985 | GGCCGGCTCTGTGCT[G/T]CCGGCTTCACAGGCG | 26094 |
rs535628206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952754 | GGCTGGAGTGCAATG[C/G]CACGATCTCAGCTCA | 26094 |
rs535639423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945305 | GGCTGAGGAGAGAAG[A/G]TCACTTGAGCCCAGG | 26094 |
rs535665448 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | DCAF4 | GRCh38.p7 | 14:72955578 | TTGCCATTGATCTGC[A/G]TTGTGGAAATCAAGG | 26094 |
rs535689862 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959738 | TTCCTGGAGAGCTTC[C/T]CTGGGCCCCTCCAGA | 26094 |
rs535855446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936256 | GGAGCCATTGTTTAG[A/G]ACAATGAATAAGATA | 26094 |
rs536017226 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956112 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACCATGTT | 26094 |
rs536124624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949173 | ATGTCACCTGGCCAG[C/G]CATGGTGGCTCCCAC | 26094 |
rs536290863 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961334 | GCTGTGTCCTGCTCA[-/T]TTTTCCAGGCCCAGG | 26094 |
rs536292745 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938129 | CTGGCATTGTACACA[C/T]GGCATGTCACACGAT | 26094 |
rs536375470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944239 | TGACTCTGGCTGGCC[A/G]GTGTGACCGCAGGGC | 26094 |
rs536501101 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947272 | GTGGGCTTCATGACA[C/T]GGCATCTTAGTGACC | 26094 |
rs536628517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946359 | GCAGTGAGCCATGAT[C/T]GTGCCACTGCACTCC | 26094 |
rs536638597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957074 | AATTAACTGGGCATG[A/G]TGGCACCTGCCTGTA | 26094 |
rs536654276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949806 | ATTTTTAAAAGTTAC[A/G]TGATTGCTTTTCAGA | 26094 |
rs536693158 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952642 | GTAATTGGGAAAGGG[A/T]TGTGAGGGAGGCCTC | 26094 |
rs536795003 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931406 | AAATACAACTGGTTT[G/T]TCTATATTGATCTTG | 26094 |
rs536851812 | snp | A/G | 0.284733 | 0.247575 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930641 | TGTGTATGTGTGTGT[A/G]TATATATATATATGT | 26094 |
rs536851989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938312 | GACCACTCTCTGTTC[C/T]TTCCTAAGTGACCAC | 26094 |
rs536883294 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954142 | GGCAGCCACACTTTA[C/T]ATTCTCCTATCCCCT | 26094 |
rs536981829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927843 | TGAAGTATTTCTTAA[A/G]TAAGTGTTAAGAGAA | 26094 |
rs536990705 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924981 | CAATGGCGCTATCTC[A/G]GCTCACTGCAACCCC | 26094 |
rs537115826 | snp | A/G | 6.59729e-05 | 0.005743 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954423 | GACCAACGTGGTGAC[A/G]GGACACCGGCAGTCC | 26094 |
rs537123814 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | DCAF4 | GRCh38.p7 | 14:72947164 | CGGTGTGCTGGGCCT[C/T]GCTGAATCACTTGGA | 26094 |
rs537240453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934832 | TCACATGGAGTGGGC[A/G]CTTTGTAAATGTGTG | 26094 |
rs537254828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940705 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 26094 |
rs537254869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934266 | TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 26094 |
rs537321326 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942623 | TATCCTGGGGCTCTT[A/C]CCGGCAGCCGTATCC | 26094 |
rs537421449 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960891 | CCCCACCTTTTTTTT[C/T]TTTTGAGACATGGTC | 26094 |
rs537463033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931236 | CATATATTAATTTTG[C/T]TAAATATATTCCTAA | 26094 |
rs537475773 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928408 | CATGTTGGCCAGGAT[C/G]GTCTCACATATCTGC | 26094 |
rs537484376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960394 | ACCTCAGGTGATCTG[C/T]CCGCCTCAGCCTCCC | 26094 |
rs537518445 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942743 | GATGCAGACACAACT[C/G]CCTCTAACTCCCACT | 26094 |
rs537626152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951214 | TCGAACTCCTGGACT[C/G]GAGTGATCCTCCTGC | 26094 |
rs537635023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948254 | GTGCAGTGGTACAAT[C/T]ATAGCTCACTCCAGC | 26094 |
rs537686656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955178 | AAAATGCCGTCTTCC[C/T]TTAAAAGTGAATGAA | 26094 |
rs537722338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945058 | GGTGCCACTGTACTT[A/C]AGCCTGGGCGACAGA | 26094 |
rs537868343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924377 | ATCCTCATTCTAATC[C/T]GTGAAGAAACTGAGG | 26094 |
rs537903096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957568 | TCAACACCAGGACTT[C/T]GCCTCCTTTTTAAGT | 26094 |
rs537950625 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942375 | GACTCCAACACCTGA[A/G]CGCCCAGCGCTGCGT | 26094 |
rs537987513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933185 | AAAATGTCTCCAGAC[A/G]TTGCCAGATGTCCCC | 26094 |
rs538077050 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926499 | TTCGCTCCAACTCCT[A/G]CAGAGCTGAGCCGGA | 26094 |
rs538089386 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950684 | GCTCATGTGAACAGA[C/G]ACACCCACATGTAGT | 26094 |
rs538167467 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958993 | ATTTGAGTTAAATTG[C/T]TGGCTGAGAGAGCTT | 26094 |
rs538370755 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926146 | GCATCACCCTGCGGA[A/G]GGAGGAAGACACGGT | 26094 |
rs538490282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951962 | GAGAAGTATGGGGCC[A/G]CTGCAGAGGCACTGT | 26094 |
rs538513953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955357 | CCACTAACAAGGAAT[C/T]ATCCTCCCTTCCAAC | 26094 |
rs538533227 | in-del | -/CTA | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949588 | GGTGAAACCCCATCT[-/CTA]CTAAAAATACAAAAA | 26094 |
rs538675089 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956908 | GAAAAGAAGTTATGG[A/T]CATTGTAAAGATTCT | 26094 |
rs538732439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949682 | ATTGCTTGAAAACCC[A/G]GGAGACAGAGGTTGC | 26094 |
rs538759109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936180 | ATTAATAAATACAAC[C/T]GTATTCTTTAGCTGG | 26094 |
rs538867192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937218 | AGGAGACATTAACAT[A/G]TGGGGGAACAGATAG | 26094 |
rs539081811 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960366 | TGTTGGTCAGGCTGG[C/T]CTCAAACTCCTGACC | 26094 |
rs539093701 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951559 | GAGGTTGCGGTAAGC[C/G]GAGATCGCGCCATTG | 26094 |
rs539132885 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929166 | CCTTGGGCCTATTGA[C/G]GCCAGGCCTGGAATG | 26094 |
rs539229634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937826 | CAGCCCTTCCCAGGT[A/C]AGGCTTGCTGTGGCA | 26094 |
rs539243703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943768 | CAAGCCCTATCCTTC[C/G]TGGAGGCTGAGGGAA | 26094 |
rs539247726 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940259 | CTGAAAAGAAACGCT[A/T]CTTCCGCTTGCTCCC | 26094 |
rs539380621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934230 | GCTATCTCGGCTCAC[A/G]GCAACCTCCACCTCC | 26094 |
rs539466742 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927043 | TTGTCAGACGCAGAA[A/G]GGGGTGCAGTTTGGT | 26094 |
rs539506354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952482 | CAGTGCCTGGTATTT[A/C]ATTGCACAGCAAGCT | 26094 |
rs539511115 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960297 | TTGGATTATAGGCGC[A/C/G]TGCCACCACGCCTGG | 26094 |
rs539514255 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926650 | GAGGAAGGCCAGGGA[A/G]AGGGGCGGGGAGGGG | 26094 |
rs539540323 | in-del | -/AGAT | 0.00529312 | 0.0511717 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949146 | ACACATCACATACTC[-/AGAT]AGTCAAGAATGTCAC | 26094 |
rs539689529 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924975 | GGAGTGCAATGGCGC[C/T]ATCTCGGCTCACTGC | 26094 |
rs539694482 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953830 | TGTGTGTGTGTGTGT[A/G]TATACACACACACTT | 26094 |
rs539900815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948701 | GTGGCTCGCCCTCTG[C/G]TGGCCATTTCTGGTA | 26094 |
rs540072272 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960843 | AGTACTCCCTGATAC[C/T]AGCTAATAAGCACCT | 26094 |
rs540084877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949282 | AGAAAGACCTCTCTA[A/C]AAAAAAAATAATAAT | 26094 |
rs540101729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942855 | CTGGGATCTTGCTCA[C/G]CTCCATTGCTGAGAA | 26094 |
rs540261182 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961791 | ACCACACCCAGGGGA[A/G]TGGGGAAGCCAAGAG | 26094 |
rs540271513 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945395 | GAGACCCCACCTCTT[-/A]AAAAAAAAATAGCCT | 26094 |
rs540271702 | snp | A/G/T | 0.00028534 | 0.0119412 | missense, utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72938010 | GGCAGAGTAGAAGAC[A/G/T]ACATGGGAGAAGAAG | 26094 |
rs540486867 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939252 | CATCCTTCAGCCTAT[A/T]ATTCCCTCAGAAGCT | 26094 |
rs540491673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937622 | GATGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 26094 |
rs540594169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957722 | CAGCTTCAGCCAAGA[C/T]AGCACTTCTGGTCTT | 26094 |
rs540889955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950866 | AAATATATGTAGTGG[A/T]AATACAGCATGGCTT | 26094 |
rs541015271 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950631 | CACGTAGGCAAGGGT[A/G]TAAAGGGGCAGGTCA | 26094 |
rs541031051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933922 | CCATAATGTGTAAGC[A/G]AGTTCATCTCACCTG | 26094 |
rs541219354 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928693 | TTATATTGGCAAGAT[G/T]GTGCAACCATCACCA | 26094 |
rs541358280 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961446 | CACTCCTCTACTCAC[A/G]TGATCCTTTGTACCA | 26094 |
rs541416269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947876 | CACGGTAGTACAGTG[C/T]CGTGGTCCCTGGCCT | 26094 |
rs541619516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935681 | CCCAAATTGGCATTC[A/G]CCAGTGATTTTATCA | 26094 |
rs541750695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932690 | TCGAGTGCTTCCTAC[A/G]TAGAACAGGTTTTCT | 26094 |
rs541784776 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961038 | GCCCACAGGTGTGCA[C/T]CACCACACTCAGTTA | 26094 |
rs541790191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944045 | CTCTTGTGGTTGGTT[C/T]CCCTCAGCAGCCCCT | 26094 |
rs541827626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950795 | GAGATATTCCATGCA[A/C]TGCCATTTCTGTATG | 26094 |
rs541845118 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929183 | CCAGGCCTGGAATGG[C/T]GCCCTGGAAGCAGGA | 26094 |
rs541852928 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939549 | GACCTCACAAAATGC[A/G]CGAGTGAGAAGATAA | 26094 |
rs541871453 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959049 | TCTTTCCTTTTCTTA[C/T]TGAATTCTTAGAACT | 26094 |
rs541873522 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951511 | AGCTACTCAGGAAGC[C/T]GAGGCAGGAGAATCG | 26094 |
rs541935070 | snp | A/G | 0.000131937 | 0.00812103 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958631 | CCAGGACTGCTACAC[A/G]AGAATCTGGAGCCTC | 26094 |
rs542016270 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930583 | CCTAAATAATGTCTT[C/T]CGATGCACGGAAGTT | 26094 |
rs542057359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952102 | AGAGCAGACTTAACA[C/T]GCATGTAAACCAGCG | 26094 |
rs542084106 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941375 | CATATTTTGTTGTCA[A/G]GGTAGGCAATGGAAT | 26094 |
rs542135488 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925503 | TTAGCCTGAAATCCT[A/G]GCTTCCTGGTTAAGA | 26094 |
rs542269064 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961710 | CAGAGGCTCAGGACA[C/T]TTGAGGATTGCGTGT | 26094 |
rs542451462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945560 | TGGCACATGACACAT[C/T]CCTCTGGGTGGATGC | 26094 |
rs542457093 | snp | A/G | 1.71322e-05 | 0.00292674 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955499 | TCATGATAGCCAGGC[A/G]CTGAGCAGTCCCTCT | 26094 |
rs542658727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943315 | CATCATCACCCCCCA[C/G]TTCAGCTCCGTCGTT | 26094 |
rs542912289 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948722 | ATTTCTGGTAGCCTT[C/G]GGGCTTTTGTGCTGA | 26094 |
rs543033534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929352 | TAGAGGGTGGTCCAC[A/G]TATTCTGTGCACTAC | 26094 |
rs543033581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937479 | GTGCAGTTTACAGTG[A/C]GCACAATCTCAGCTC | 26094 |
rs543050319 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926522 | GAGCCGGAGGGGAAT[C/G]CGGAAGGGACACGCT | 26094 |
rs543169395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930026 | AATTCCGGCTACTCC[A/G]AGGTTGAGGCAGGAG | 26094 |
rs543263838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926738 | CGGCGCGCTCCGCCC[A/G]TTCTGGGGCGCGTGG | 26094 |
rs543273467 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954893 | AGGCCAAGATGGGTG[A/G]ATCACAAGGTCAGGA | 26094 |
rs543278671 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950548 | AATGAGAATAAATAC[A/G]GGCTCCTCTGGAACA | 26094 |
rs543428925 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952399 | GGAATGTTGAACCTC[C/T]CTAAAGTGGACAGGG | 26094 |
rs543429504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946723 | ATAAGAGGAGCTTGC[C/T]GTCTAGGGAGCAACC | 26094 |
rs543453456 | snp | A/T | 9.88598e-05 | 0.00702995 | missense | DCAF4 | GRCh38.p7 | 14:72945999 | TCAAGGTGTTCATGC[A/T]CGAAAACCTCTACTT | 26094 |
rs543490940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939470 | GCTGACAAATGAGCC[C/T]AGCTGGTAAAATTCT | 26094 |
rs543517971 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933698 | CTGTATTCTCAGACC[C/T]GTATTTCCCATTGCC | 26094 |
rs543602051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927229 | TTGTCTTGTGACTCC[A/G]GCAGCGCAGCCAGAA | 26094 |
rs543681197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935607 | ACTTGAGGTTGGCAG[A/G]CTCCCTTACCAGATT | 26094 |
rs543778455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953979 | ACAAAGATGCATTTT[C/T]GGAATAACCACTTGT | 26094 |
rs543784393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928280 | CTCACCGCAACCTCC[A/G]CCTCCCAGGTTTAAG | 26094 |
rs543899678 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943887 | GACCCTGGAGGTTGA[C/T]ACTGCATCCTCCTGC | 26094 |
rs543929436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950090 | GGCTAGGGAGCAGGG[C/T]CTTTCAAGACTGAAT | 26094 |
rs543993410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956955 | CGGTGGCTCACGCCC[A/G]TAATCCCAACACTTT | 26094 |
rs544051270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943944 | TTCCATGTAAGGGGT[G/T]TTGGGGACCGGGCCC | 26094 |
rs544228444 | snp | A/G | 5.5746e-05 | 0.0052792 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956412 | GGACCTGAGGACCAC[A/G]AAGTGCGTAAGGCAG | 26094 |
rs544454052 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933686 | CTCAATTTCTCTCTG[C/T]ATTCTCAGACCCGTA | 26094 |
rs544537627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945528 | GCATTTTTCCTATTG[C/T]GCCACAGCCTTCGTG | 26094 |
rs544600594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951468 | AATACAAAATTACCC[G/T]GGCGTGGTGGCACAT | 26094 |
rs544605290 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924633 | GTCCCCTGGCTCTTC[A/G]GTGGAAAATCCAGCT | 26094 |
rs544686626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927483 | CAGCTTCCCGCGTAG[C/T]TGGGGCTACAGGCGA | 26094 |
rs544728205 | in-del | -/TG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930631 | CAATTTATGTGTGTA[-/TG]TGTGTGTGTGTATAT | 26094 |
rs544735725 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944655 | AAATTAGCTGGGCAT[A/G]GTGGTGTGTGCATAT | 26094 |
rs544771755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960473 | AAATATATTTAATCC[A/G]TCCGCCCCAGTTATC | 26094 |
rs544827442 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936708 | TGTTGGGTCTGTGGA[-/G]GATAGACACGAAGCA | 26094 |
rs544831737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950967 | AGGGATCAGAGAGGG[C/T]TTTTTGGGCTTTTTA | 26094 |
rs544907326 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954243 | CCTGAATATCCAAGC[A/G]AATAACTGCTTCAGT | 26094 |
rs544985514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928085 | GGATTAGAGGCGTGA[G/T]CCACCGCCCTGGCCT | 26094 |
rs544997951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935105 | CATGGACTATAAAGC[A/G]GCCATAGAGAATGAA | 26094 |
rs545059659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72935960 | TTTTCCTATCAGTCT[C/T]TTTCTCTTTTTGAGA | 26094 |
rs545221762 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961098 | CCCTATGTTTCCCAG[G/T]CTGGTCTTGAACTCC | 26094 |
rs545268013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929892 | GGTCACCTTGTGGCC[A/C]TTGTTGAGGCCCACG | 26094 |
rs545280076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947917 | TGGGGGCTGTTGATA[C/T]GGCACAAGACTTGAC | 26094 |
rs545307397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954623 | GGATCAGTGGGTTCC[C/T]TTGTAAGGGTGTCTG | 26094 |
rs545455026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936457 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 26094 |
rs545462399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948485 | GGGTTCTGTAGGCCA[A/G]TGGGACTGACCACAT | 26094 |
rs545551434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939301 | CAAGTGTTTTAGCCG[C/T]AGCTCTATCCCAGTG | 26094 |
rs545588292 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926223 | CCCCGGCCCCGCCCC[C/T]GCGTGCGCCTGGCCC | 26094 |
rs545686208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932810 | CTGGACTCAAGCCAT[C/T]CTCCCACCTCAGCCT | 26094 |
rs545709812 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962316 | ACCCCAGGATCAGAG[A/C]TGGCTACTGTTTCCA | 26094 |
rs545714781 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950169 | ATTTTTGAAAATGAT[C/T]CCTTTGGTGGCATTG | 26094 |
rs545723756 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961927 | GGAAGGTTTGGCTAC[C/T]GCGGGAACACCCCAG | 26094 |
rs545767550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938639 | AATTGCTCCGAGGCT[A/G]CAAACCTGTACAGCA | 26094 |
rs545876168 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941523 | GGGAGCGTGGGCAGA[A/G]TTGACGAGCAGACTT | 26094 |
rs545910865 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959179 | AGCCCAGTGATGAGA[C/T]GGTGAGATGGTTTGA | 26094 |
rs545969923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940454 | TGTTGAAAAGGGTGC[A/C]AATTAGATGCCCCTG | 26094 |
rs545973448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933504 | GCAGAGGTTGCAGTG[A/G]GCCGAGATTGTGCCA | 26094 |
rs545975606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948095 | CTAGCAGTTTCTGGA[C/T]ATCATTGGTCCTCGA | 26094 |
rs546005128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952149 | TCGGACGCCCGTGCA[C/T]ATCATTCAGAAAACA | 26094 |
rs546032908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946666 | TGTGTCAGAGTGATG[C/T]GTCATCCAGCCAGGC | 26094 |
rs546073454 | snp | A/C/T | 4.94893e-05 | 0.00497419 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958676 | ACTGAGAACCATACC[A/C/T]TCCCCGTACCCTGCC | 26094 |
rs546224684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955004 | CCTGTAATCCCAGCT[G/T]CTCGAGAGACTGAGG | 26094 |
rs546302029 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959948 | GTTGGGCTGTGGGTG[A/G]CTGTAACCAAAACCC | 26094 |
rs546397341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941579 | GCCTTTCCTCTTGCC[A/G]AGGAAGGGAGACTTG | 26094 |
rs546422365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940032 | GGTGCGTCAGGAATG[A/G]TGGTCATGAGGCAAA | 26094 |
rs546461041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936683 | AGAAATCATGAACTC[A/G]CTTTTGAACCTGTTG | 26094 |
rs546633029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942450 | AGGCAGCTTCCTGGG[C/G]CACAGCCCTCGGACC | 26094 |
rs546789739 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962495 | TCTTTACAAAACACA[C/T]ACACACACACACACA | 26094 |
rs546819975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936132 | ACGTGCTTCCCTTCC[C/T]GTGCGCAGTCCCTTT | 26094 |
rs547135548 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948819 | GACCTGCACTCTGCA[C/T]TTTTCCTGCAAGAGT | 26094 |
rs547199942 | in-del | -/TTTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927364 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGGCGGAGTCTCGC | 26094 |
rs547203376 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945115 | CCACATCCTGAGCGA[-/G]GGCATGGTGCCTCAC | 26094 |
rs547229450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937796 | GTGGGAAGGATGTTG[C/G]GGGAGTGCTGGAGGC | 26094 |
rs547252819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949616 | AAAAATTAGCCAGGT[A/G]TGGTGGCACGCACCC | 26094 |
rs547335884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943736 | CGATGGACCACGTAA[A/G]AGCAGGGCCTGCCCG | 26094 |
rs547396883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946253 | AAAAAAAATTATTTG[A/G]GTGTGGTGGCGCGCA | 26094 |
rs547432104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934223 | CAATGGCGCTATCTC[A/G]GCTCACGGCAACCTC | 26094 |
rs547454257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927636 | GATTACAGGCGTGAG[C/T]CACCGCGCCCGGCCT | 26094 |
rs547605919 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946611 | TTCCTTGGAAATGGG[C/T]GACAGTGACTGTGGC | 26094 |
rs547673612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947032 | AGCCCATTTGAAGAG[C/G]AGCAGGACGTGAAGA | 26094 |
rs547683652 | snp | C/T | 3.31159e-05 | 0.00406901 | missense | DCAF4 | GRCh38.p7 | 14:72954391 | TCTCCGCCAGGCTTG[C/T]CTCGGCGGGTCCTGT | 26094 |
rs547848561 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930352 | CGGCTCACTGCAGCC[G/T]CCACCTCCCGGGTTC | 26094 |
rs547874723 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953489 | CCAAGGCAGGATAAT[C/T]GTTTGAGCCCAGGAG | 26094 |
rs547911711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950359 | GATAGACCTCCCAGA[C/G]AGTGGTGGGTTGAGG | 26094 |
rs547969047 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959568 | TGACTTTTTGTAATC[C/T]AGGAGCGACAGTTCG | 26094 |
rs547985280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930877 | CACTTCTTTCTTTCA[C/T]TGAATGGTCTTGGCA | 26094 |
rs548070339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957330 | GAAGGGAGTTACCAG[C/T]TGATTACAGATGATG | 26094 |
rs548081653 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72960728 | TCCATTTCCAGCCTC[A/G]TGATGGTTCCTGGGC | 26094 |
rs548170108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937671 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 26094 |
rs548204782 | snp | A/G | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957979 | GCCCATCCCCAGGAT[A/G]TAATGACTTTGACAG | 26094 |
rs548204978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950599 | AAGGAGAGGAACCGC[C/G]TCAGTCAAAAGACAC | 26094 |
rs548347131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944870 | GAGATGGGAGGATCA[C/T]TTGAGGTCAGGAGTT | 26094 |
rs548541389 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938765 | TTTTTAAATGGTATA[C/T]CTATGTATGACACTC | 26094 |
rs548679856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944252 | CCGGTGTGACCGCAG[A/G]GCCAGAAAGTGGCTT | 26094 |
rs548729921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953431 | AAAAAATATTTTTTC[A/G]AAGCACAGTGGCTCA | 26094 |
rs548741983 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939550 | ACCTCACAAAATGCG[C/G/T]GAGTGAGAAGATAAG | 26094 |
rs548822790 | snp | A/G | 0.000164715 | 0.0090736 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72947165 | GGTGTGCTGGGCCTC[A/G]CTGAATCACTTGGAT | 26094 |
rs548861408 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945736 | AGTTGGGGAAAGTGA[A/G]GTCATCTCCACTCTC | 26094 |
rs549018567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947607 | GTGGTAGCAGAGGAA[C/T]AAGGCAGAAAGGAGC | 26094 |
rs549060495 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937581 | GCACGTTACAACTCC[C/T]GGCTAATTTTTGTAT | 26094 |
rs549176539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935431 | AGTGAACTGTTGTAC[C/T]TTTAGTAGAGACGGG | 26094 |
rs549264466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936113 | CAGTCTTAACACTGG[C/T]CACACGTGCTTCCCT | 26094 |
rs549363568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949505 | CATTCCCATAATCCC[A/G]GCACTTTGGGAGGCT | 26094 |
rs549498951 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961580 | CCCAGAATTTCTGGC[C/T]CCTCCTGTCCCAGCA | 26094 |
rs549512428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932082 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 26094 |
rs549607790 | snp | A/C/T | 3.29746e-05 | 0.00406035 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943012 | AGCCCACGAGCTGCG[A/C/T]CTCAGCTGCATGGAG | 26094 |
rs549625610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955846 | AGGCCCTGCATGGGG[A/G]CTGCTTCGTTGACCA | 26094 |
rs549822389 | snp | A/C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926256 | CCCCCAAGCGCTCCA[A/C/T]GACCAGCCTCCACGT | 26094 |
rs549829097 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934130 | GCCTGCAGGCCCCCC[C/G]CCCCCACTGCCTTAC | 26094 |
rs550005030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952229 | CTGCCTACGTTAAGG[C/T]AATTTGACTCCTCCT | 26094 |
rs550110192 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72926962 | GGTGTGGTTGAAGCT[A/T]ACGAAGTGGCCGGCT | 26094 |
rs550187189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946188 | GGAGTTTCAGACCAA[C/T]CTGGGCAGCATAACA | 26094 |
rs550246970 | snp | A/G | 0.00107906 | 0.0232027 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943125 | GGACACCTGCCTAGG[A/G]TGTGGCTGCCACCCT | 26094 |
rs550452021 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962523 | ACACGCATGCACACT[C/G]TCTCTCTTAGCCCAG | 26094 |
rs550489803 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930259 | TTCTTTTTTTTTTTT[C/G]AGACGGAGTTTTTTT | 26094 |
rs550551074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955416 | CGTGTCTAATCACAC[C/T]GTCTGACCCAGAGGC | 26094 |
rs550800603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929550 | ACAAAAATATTTTTT[A/T]TTTTTATTTTATTTT | 26094 |
rs550811919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957206 | ACAGAGCGAGACTCC[A/G]TCTCAAAATAAATAA | 26094 |
rs550845694 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960960 | AGCACAATTACTACT[C/T]ACTGCAGTCTTGACC | 26094 |
rs550983298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956824 | AGCATTATTCCACCA[C/T]GCAACTATCTTATCC | 26094 |
rs551071154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949728 | CGCCACTGCACTCCA[C/G]CCTGAGCGAAAGAGC | 26094 |
rs551349372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934763 | CCATATTAAACAATC[A/G]GTGCCTCCAAGCCAG | 26094 |
rs551497969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946318 | GGTGAGGTGGGAAGA[C/T]CACCTGAGCCCAGGA | 26094 |
rs551556858 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928874 | CAGCCCCGAGGCCCC[C/G]AAACTGGAGAGCCCC | 26094 |
rs551575456 | snp | C/G | 0.00358779 | 0.0422022 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960878 | TATGTCAGGCCCCCC[C/G]CACCTTTTTTTTTTT | 26094 |
rs551724398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947535 | CTGCCACTGTGGCGT[A/G]TGACGGGAGGCTCTG | 26094 |
rs551737924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928382 | GTATTTTAGTAGAGA[C/T]AGGTTTTCACCATGT | 26094 |
rs551816519 | in-del | -/ATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953733 | AAAAAAAAAAAAAAA[-/ATA]TATATATATATATAT | 26094 |
rs551871596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931036 | GAATTTTGAAATTGC[A/G]AGGTGCGAGTCATCC | 26094 |
rs551961506 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925606 | CAGGGGCCTGTGTTA[C/T]GGAGCCGCATGACAC | 26094 |
rs552033743 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961517 | TGGGTCAGAGACAAG[G/T]GTGAGATTTTTCTCA | 26094 |
rs552047783 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951137 | AGGCACACACCACCA[C/T]GCCCAGCTAGTTTTT | 26094 |
rs552184130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951626 | CAAAAACAAACAAAC[A/C]AAAAAAAAACATCTG | 26094 |
rs552189898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944981 | GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGTGG | 26094 |
rs552196531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930465 | GTAGAGACGGGGCTT[C/T]GCCATGTTTATCAGG | 26094 |
rs552278010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945727 | GCTGCACTAAGTTGG[A/G]GAAAGTGAGGTCATC | 26094 |
rs552320003 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957444 | CAGTCTTCAAGAATT[G/T]TCACCTCTACTGGTA | 26094 |
rs552350945 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939703 | GGTCAGAGATCAGAG[A/G/T]TGAAGGCTGCAGAAC | 26094 |
rs552646680 | in-del | -/AACA | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935058 | TGAGATGGGAGTATG[-/AACA]AACAGTCATGCAGAG | 26094 |
rs552664669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938832 | TGAGTGATGAGTGAA[A/C]ACAAAGGCTTAGGAC | 26094 |
rs552720240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933974 | TTGTCACCCCATGCC[A/G]CTGCCTTTCAGGTGC | 26094 |
rs552751940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935491 | AACTCCTGACCTCAG[A/G]TGATCCACCCGCATC | 26094 |
rs552789106 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926366 | CGTCGACAGACAGAA[C/G]CCGCGTCCAGTGAGA | 26094 |
rs552898578 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933326 | AGCACTTTGGGAGGC[C/T]GAGATGGGCAGATCA | 26094 |
rs552965423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940801 | TCACCATGTTGGCCA[A/G]GTTGGTCTTGAACTC | 26094 |
rs553030220 | snp | A/G | | | utr-variant-3-prime, missense | DCAF4 | GRCh38.p7 | 14:72960618 | TGGTGGCACAGGAAG[A/G]GATGGCTGGATAGTA | 26094 |
rs553053297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934954 | GTTCAGCAAAAATTT[A/G]CTAAGCACCAACTAG | 26094 |
rs553063089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928054 | TATCCTCCCACCTCA[C/G]CCTCCCAAAGTGCTG | 26094 |
rs553157083 | in-del | -/TTTTTTTTT | 0.222928 | 0.24853 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927344 | GTCGCGGTGGTGTTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs553250744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928499 | CGCGCCCGGCCAGTC[C/T]ACAGACTCTTACAAA | 26094 |
rs553274590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929223 | TAATTCCGGAAGCTG[A/C]GGGCTCCCAAACCAG | 26094 |
rs553377086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947878 | CGGTAGTACAGTGTC[A/G]TGGTCCCTGGCCTCT | 26094 |
rs553414325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937016 | TAATCAATAGCAAGA[A/G]CATTTTAGTAGAAAG | 26094 |
rs553431218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942708 | CTTTCGTCATCTCAG[C/G]GGAAGGAGCTGTACT | 26094 |
rs553511879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948392 | TAAATACATTAGCGA[C/T]CTGATTATAAATTTA | 26094 |
rs553568208 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936409 | TCTCTACTAAAAATA[C/G]AAAAATTAGCTGGGT | 26094 |
rs553639951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943182 | CAGTCATCAAACCTG[A/G]CTCTGGAGAAGCCAA | 26094 |
rs553716011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939183 | ACACGGCGAAACTCC[A/G]TCTCTACTAAAAATA | 26094 |
rs553732676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927006 | TTCACAGGCGCTAAC[A/G]TTTGCCAGCGCTATG | 26094 |
rs553776958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950830 | TTTTTAAACAAAAGC[C/T]GCTTTGTGTTATTTA | 26094 |
rs553778602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958478 | TCCGTAGAAATACTG[C/T]CCGTTAATGAGTTTG | 26094 |
rs553794357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926593 | CGATTCGAGGGCTGC[C/T]GCGCTCCCGCTGCAG | 26094 |
rs553840845 | in-del | -/C | 0.00557542 | 0.0525036 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959763 | TCCAGACCCACTCTG[-/C]CCTCATCATCTGTCC | 26094 |
rs553915965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951332 | AACATCTGAAGCTGG[C/T]CAGTCACGATGGCTC | 26094 |
rs554056015 | snp | A/G | 4.1934e-05 | 0.00457878 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939854 | GGCCACGGTGATGAC[A/G]AGTCTCCGTCAACCT | 26094 |
rs554221472 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959783 | ATCATCTGTCCATCT[C/G]CACCCTGCTCTGTGC | 26094 |
rs554231103 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962209 | GGCCTATGCCCTTGC[A/G]CTCGGAGAGGCTTCA | 26094 |
rs554315047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956210 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCCTGGTT | 26094 |
rs554441473 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949815 | AGTTACATGATTGCT[A/T]TTCAGATATTTACAT | 26094 |
rs554453933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956905 | TGAGAAAAGAAGTTA[C/T]GGTCATTGTAAAGAT | 26094 |
rs554589584 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938189 | TCCCAATGCAGGTTC[A/T]GATTCTGTAGGTCTG | 26094 |
rs554667504 | in-del | -/AGAT | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937232 | TATGGGGGAACAGAT[-/AGAT]GTCTGCAGTTCCTGG | 26094 |
rs554693543 | snp | C/G | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958959 | CTGAATGTTCCGTGT[C/G]GAGATGCTCAGGAAA | 26094 |
rs554700035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943862 | GGACTGGAGGCCGAT[A/G]CTAGAGATTGACCCT | 26094 |
rs554783404 | in-del | -/T/TT | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937410 | GCAATTTTTCTTTTC[-/T/TT]TTTTTTTTTTTTTTT | 26094 |
rs554842975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943328 | CACTTCAGCTCCGTC[A/G]TTTAACGTCAGAGTC | 26094 |
rs555057086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930643 | TGTATGTGTGTGTGT[A/G]TATATATATATGTAG | 26094 |
rs555124811 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954287 | GCTCCCCAGGTGCCC[A/G]GAGAAGAGGCCTTAA | 26094 |
rs555189026 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924521 | TGCCCACGTCACTGT[A/C]CCCTCTGTGGACATT | 26094 |
rs555197710 | snp | C/T | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961672 | TCTGTCCCTCAACCT[C/T]ACCAGCCCTTGGCTT | 26094 |
rs555244924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931410 | ACAACTGGTTTTTCT[A/G]TATTGATCTTGTATC | 26094 |
rs555286248 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952235 | ACGTTAAGGCAATTT[C/G]ACTCCTCCTTCCTGA | 26094 |
rs555448205 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935935 | TAATCTTTATGTCAG[C/T]AGAGTTTATTTTTCC | 26094 |
rs555594347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936286 | AAAAGTTTTGGAGCC[A/G]GGCTTGGTGGCCCAC | 26094 |
rs555642830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934886 | CAGAGCAGAAAGAAG[C/T]TACCTGGGACTTAAA | 26094 |
rs555685433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960396 | CTCAGGTGATCTGCC[A/C]GCCTCAGCCTCCCAA | 26094 |
rs555771210 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954025 | GCTGAGTCTCTCTTG[A/C]AACCACAAAACCCAG | 26094 |
rs555779153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947341 | AGAAAAAAAAGCAGC[A/G]TACCTGGATAGAACA | 26094 |
rs555816112 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949469 | TCTTAAAAAAGAGAA[A/G]AGTGACTGGGCACAG | 26094 |
rs555970610 | snp | A/G | 1.88898e-05 | 0.0030732 | missense | DCAF4 | GRCh38.p7 | 14:72956468 | CCTACCTGCCCCTGC[A/G]TGTGCACGAGGAAGA | 26094 |
rs555991471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939091 | GGGTGTGGTGGCTGA[C/T]GCCTGTAATCCCAGC | 26094 |
rs556115801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933207 | GATGTCCCCTGGTGG[A/G]CAAAATAATCCTTAA | 26094 |
rs556116957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944627 | GGTAAACCCCGTCTC[C/T]ACAAAAAAATATAAA | 26094 |
rs556224552 | snp | C/T | 0 | 0 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950144 | CCCAGGGGGTTGTGA[C/T]TGTGGAGTCATTTTT | 26094 |
rs556303693 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959003 | AATTGCTGGCTGAGA[C/G]AGCTTGGAAGTCCTT | 26094 |
rs556319970 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941185 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 26094 |
rs556353854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951250 | CTTCCCAAAGTGCTG[A/G]GATTACATAGGCAGG | 26094 |
rs556434172 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926826 | GTCGCCGCTGAGGGC[C/G]TTTCTCTAAGCGCTT | 26094 |
rs556548266 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957881 | GTGTCACAGTCCTCA[C/G]AACTGGAGCCCTGAA | 26094 |
rs556584851 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926535 | ATCCGGAAGGGACAC[G/T]CTGAACAGGTAAGAC | 26094 |
rs556659548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936187 | AATACAACTGTATTC[C/T]TTAGCTGGGGTATAA | 26094 |
rs556786094 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959983 | CTTCTATTGGAAAGC[A/G]CTCAGAGAGAGCCGG | 26094 |
rs556841709 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962178 | GGAGAGGAGGTGAGA[C/T]GAGAAGGGCTTCTCA | 26094 |
rs557128973 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929210 | AGGAAAGAGCCTGTA[A/G]TTCCGGAAGCTGCGG | 26094 |
rs557215285 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948489 | TCTGTAGGCCAATGG[C/G]ACTGACCACATGTTA | 26094 |
rs557227440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955402 | AACCCTGACCAGCAC[A/G]TGTCTAATCACACCG | 26094 |
rs557249378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930575 | TGTCCGGCCCTAAAT[A/T]ATGTCTTTCGATGCA | 26094 |
rs557416288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942754 | AACTCCCTCTAACTC[A/C]CACTCTTTGACTCTG | 26094 |
rs557441647 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926200 | AGTTCCGCTGCTCCG[A/G]GAGCAGCCCCCGGCC | 26094 |
rs557442458 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937220 | GAGACATTAACATAT[C/G]GGGGAACAGATAGAT | 26094 |
rs557496545 | in-del | -/ATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[-/ATATATATA]TATATATATATATAT | 26094 |
rs557504192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943260 | GCCTGCTGGCTACCC[C/G]CTGGGAGACGCTGAG | 26094 |
rs557572535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929923 | GCCATAAGGTAGCGC[A/T]GAGCCATGGCTGCTG | 26094 |
rs557763998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951943 | TGTGTGGGGGTGGCT[C/T]AGAGAGAAGTATGGG | 26094 |
rs557791289 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926715 | CCGGGCCTAGGTGGC[A/C]GCTGGGCCGGCGCGC | 26094 |
rs557814253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945490 | AAAAAAAAAAAAAAA[C/T]AGTGCCTATGTAATA | 26094 |
rs558044314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947758 | AGTGGACATGGGTCT[C/G]TGGGCTCTGGGCCTC | 26094 |
rs558057133 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925232 | CTACTCTTTCCCTGG[C/T]AATTGCTGCGTCACC | 26094 |
rs558118309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935122 | CCATAGAGAATGAAC[C/T]GTGTTTGTGTTTAGA | 26094 |
rs558147436 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945186 | TCACTTGAGGCCAGA[A/T]GTTCAAGACCAGCCT | 26094 |
rs558223199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953910 | CTCCAACAGTATACT[A/G]CCTCCCTGATATCAG | 26094 |
rs558235307 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942761 | TCTAACTCCCACTCT[G/T]TGACTCTGCAAATGG | 26094 |
rs558237542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960306 | AGGCGCGTGCCACCA[C/T]GCCTGGCTAATTTTG | 26094 |
rs558301777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950052 | GGTATGTTTGGCAGC[A/G]GTTTGATATTCATGA | 26094 |
rs558439651 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943934 | AGCAGGGCCCTTCCA[G/T]GTAAGGGGTGTTGGG | 26094 |
rs558708250 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951666 | GTGGGCAGTGTAAAC[A/G]CATGTTGAATCTGGA | 26094 |
rs558716895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938401 | GAAAACCGTTTCTCC[A/G]TTTTGTAGACTTTTT | 26094 |
rs558805251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931692 | TATCAGGTTGAGGAA[A/G]CTACCTTCTGTTTCT | 26094 |
rs558862562 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959291 | TTACTTCTCTAAGTT[G/T]CTGCAGAAATATTGA | 26094 |
rs558970358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932367 | TATAAAATGATTCGG[A/G]AAAATGTAGTAAATA | 26094 |
rs559117978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934439 | GATTACAGGTGTGAG[C/T]CACTGCACCCGGCCT | 26094 |
rs559120746 | snp | C/G | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961778 | GTTGGCATCCCATAC[C/G]ACACCCAGGGGAATG | 26094 |
rs559216663 | in-del | -/A | 0.0246078 | 0.108159 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945396 | GAGACCCCACCTCTT[-/A]AAAAAAAATAGCCTA | 26094 |
rs559242264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960457 | ACCTGGCCCGATTCT[C/T]AAATATATTTAATCC | 26094 |
rs559326563 | in-del | -/TGGGG | 0.223225 | 0.248562 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940969 | TTAGTAACTGTTTTT[-/TGGGG]TGGGGTTTTTTTGAG | 26094 |
rs559420605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928356 | ACGCCACCGCGCCCG[A/G]CTAACTTTTTGTATT | 26094 |
rs559555927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928696 | TATTGGCAAGATTGT[A/G]CAACCATCACCACTG | 26094 |
rs559603864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942017 | CTGTTCTCTCTAGAG[C/T]GAAGGCGGGGGACTC | 26094 |
rs559671974 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947526 | CGGCTCACTCTGCCA[C/G]TGTGGCGTGTGACGG | 26094 |
rs559697846 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925537 | GAAATGCCTTCGCAC[A/G]GCGTGCAATGGGTGA | 26094 |
rs559775954 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961846 | TCTCTCTCCTTGCCC[C/G]CAAGGGCATCCTCTC | 26094 |
rs559936211 | snp | A/C | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925909 | AGACTCGCCCTAGGT[A/C]CCACAGCAAGCAGCA | 26094 |
rs559998823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938141 | ACATGGCATGTCACA[C/T]GATCACAGGTGTGGA | 26094 |
rs560037705 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961473 | ACCATTTGGTCCAAT[A/T]GATCTTGATCTCATC | 26094 |
rs560088826 | in-del | -/GAGT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939551 | CCTCACAAAATGCGC[-/GAGT]GAGAAGATAAGAAGA | 26094 |
rs560135639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958014 | TTTACTATAACATGA[A/C]AAGATCAGGCCAGGT | 26094 |
rs560200455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944693 | GCTACTCGGGAGGCT[A/G]TGGTGGGAGTATCAC | 26094 |
rs560368908 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945688 | ATTGTTAGATCAGAC[A/T]CGTGCTGGCTTTGCC | 26094 |
rs560508985 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961323 | GTTCCCCTCACTGCT[A/G]TGTCCTGCTCATTTT | 26094 |
rs560573737 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, missense | DCAF4 | GRCh38.p7 | 14:72960685 | TACCTCAACAGGAGA[A/G]GTTGGGCAGAGACAG | 26094 |
rs560669823 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960210 | TGCCCAGGCTGGAGT[G/T]CAATGGCGCTCTCAC | 26094 |
rs561011826 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936730 | CACGAAGCAGCATAG[G/T]AACTTGGTGCTCAGT | 26094 |
rs561034271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942818 | CCTGAGCGTTCTGTG[A/G]GGAAACTCAAATTCG | 26094 |
rs561107073 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942415 | CCACTGTACATGCTC[A/C]AGTGAAGAACCTGCA | 26094 |
rs561297893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929355 | AGGGTGGTCCACATA[C/T]TCTGTGCACTACATA | 26094 |
rs561319028 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948441 | GTGTGTTCTCTAAAT[C/T]GCAAATTTTATGTGG | 26094 |
rs561343758 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962417 | ATGCCGAGACAGGAG[C/G]ATTGCTTGAGCTTAG | 26094 |
rs561355583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950576 | ACAAAGTTTGGCTAT[A/G]AGGGGAAAAGGAGAG | 26094 |
rs561477351 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934246 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 26094 |
rs561603632 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953078 | CGATCTCAGTTCACC[A/G]CAACCTCCGCCTCTG | 26094 |
rs561612107 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949529 | GGAGGCTGAGGCAGG[C/T]GGATCACTTGAGGTC | 26094 |
rs561647029 | snp | C/T | 0 | 0 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926273 | ACCAGCCTCCACGTG[C/T]ATCCGCCCCAGACAG | 26094 |
rs561741158 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933193 | TCCAGACATTGCCAG[A/T]TGTCCCCTGGTGGGC | 26094 |
rs561777664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926765 | GTGGGGCCCTCCGGC[C/T]GGATCAGTGCTGCAA | 26094 |
rs561778227 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929426 | CAGATTTGCTGCCGC[C/G]CGTGGTGGCTCACGC | 26094 |
rs561799575 | in-del | -/CCTCCG | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952776 | CTCAGCTCACCACAA[-/CCTCCG]CCTCCCAGGTTCAAG | 26094 |
rs561825055 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959294 | CTTCTCTAAGTTTCT[G/T]CAGAAATATTGAAGG | 26094 |
rs561950001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952951 | ACCTGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 26094 |
rs562000465 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928651 | TAACTTTTTTAAAAG[C/G]GTTCAATCCAGTGGG | 26094 |
rs562050081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947368 | AACACAAGGATGCCC[A/G]TGGAGCACAGAGAAG | 26094 |
rs562061807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928306 | TTAAGGGATTCTCCT[C/G]CTTCAGCCTCCCGAG | 26094 |
rs562219151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940570 | CCCTTCTTCCATCCC[C/G]GTTTTCTTGTTCGAT | 26094 |
rs562235781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937685 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 26094 |
rs562247208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943525 | TAGAGGGTAGGACTC[C/T]TTGCTTGCCGCCCCT | 26094 |
rs562311370 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932770 | AGATGGAGTCTTGCT[A/G]TGTTGCCCACACTGG | 26094 |
rs562503196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957217 | CTCCGTCTCAAAATA[A/T]ATAAATAAATAAAAA | 26094 |
rs562513928 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958492 | GTCCGTTAATGAGTT[C/T]GTGTTTTGGCTCACA | 26094 |
rs562656445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930810 | TATGAAGTAAGGATC[C/G]AAATTCATTCTTTTG | 26094 |
rs562690122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957907 | CTGAAGACTTAAACC[A/G]GTCCTAGGAACTGAA | 26094 |
rs562746529 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937530 | GGTTCAAGCGATTCT[C/G]CTGACTCAGCCTCCT | 26094 |
rs562898412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960204 | ACTTGTTGCCCAGGC[G/T]GGAGTGCAATGGCGC | 26094 |
rs562907145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944828 | GTGTGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 26094 |
rs563064194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951472 | CAAAATTACCCGGGC[A/G]TGGTGGCACATGCCT | 26094 |
rs563081545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960476 | TATATTTAATCCGTC[C/T]GCCCCAGTTATCTAA | 26094 |
rs563167725 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952404 | GTTGAACCTCTCTAA[A/G]GTGGACAGGGCCTTC | 26094 |
rs563175947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928086 | GATTAGAGGCGTGAG[C/T]CACCGCCCTGGCCTG | 26094 |
rs563567137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942292 | CTTTCCCCCATTTCC[G/T]GAAGAAGAGACTGAG | 26094 |
rs563567192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944069 | AGCCCCTTCCCTGGG[A/G]TAAAGTGGGTGGGGA | 26094 |
rs563581332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941487 | ACCTGGTGGCTTCGT[A/C]CCCCCGGGTGTATGT | 26094 |
rs563702900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72935970 | AGTCTTTTTCTCTTT[C/T]TGAGATGGGGTCTCA | 26094 |
rs563787038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936462 | CCAGCTACTCGGGAG[G/T]CTGAGGCAGGAGAAT | 26094 |
rs563806147 | snp | A/C/T | 3.57062e-05 | 0.00422517 | stop-gained, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956430 | GTGCGTAAGGCAGTA[A/C/T]GAAGGCCACGTGAAT | 26094 |
rs563952561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938732 | AAGATACAGTAAAAA[C/T]AGGGTATATAAGATT | 26094 |
rs564048984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955827 | TGAAGACCAAGTGAT[C/T]TGTAGGCCCTGCATG | 26094 |
rs564241883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946122 | CTGGGGAAGAGGGCA[C/G]AGCATACTTACCTCA | 26094 |
rs564364944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940471 | ATTAGATGCCCCTGC[A/G]ACACTTAGCAGAGGC | 26094 |
rs564385720 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959200 | GATGGTTTGAGTCCT[C/T]GGTGCCTGGGTAGCA | 26094 |
rs564531970 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936520 | AGTGAGCTGAGATGG[C/T]GCCACTGCACTCCAG | 26094 |
rs564602473 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940550 | AATAAGAACAGCCAA[A/G]AGCCCCCTTCTTCCA | 26094 |
rs564622683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949366 | GAAGCTGAGGCAGGA[A/G]GATCATTTGAGCCCC | 26094 |
rs564628781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942858 | GGATCTTGCTCAGCT[A/C]CATTGCTGAGAAGTA | 26094 |
rs564710990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943460 | TGCTTCTTCCTGAAC[C/T]GGGGCAGGACTTGGT | 26094 |
rs564753313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927506 | ACAGGCGACCACCAC[C/T]TCGCCCGGCTAATTT | 26094 |
rs564816588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934471 | ATTTTTGTATTTTTA[A/G]TAGAGTTGGGGTTTC | 26094 |
rs564898349 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960857 | CTAGCTAATAAGCAC[C/T]TACTGTATGTCAGGC | 26094 |
rs565033364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930158 | TAAATAAAGTGGTAT[C/G]TCACTGTGGTTTTGA | 26094 |
rs565043400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937661 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 26094 |
rs565074633 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962407 | GGCCGAAGTGATGCC[A/G]AGACAGGAGGATTGC | 26094 |
rs565229070 | in-del | -/TTTTTTTTTT | 0.451608 | 0.147832 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928187 | ACAGAATCCCCCCAC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs565317825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930733 | TTTATACCTTTGTTT[C/T]CTTCAAAGAGTTTTA | 26094 |
rs565402170 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924571 | GCTGCCAGCCACTCA[C/T]TGACTCAGCAAGCCC | 26094 |
rs565443817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957725 | CTTCAGCCAAGATAG[C/G]ACTTCTGGTCTTAGA | 26094 |
rs565445652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950399 | GTGTAGTAGAAATTG[C/G]GCTACATGGCCATAG | 26094 |
rs565475777 | snp | A/T | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926787 | GTGCTGCAACCGTAA[A/T]CACGCAGGGAGGGCA | 26094 |
rs565568435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944813 | AAAAAATAGGGCCAG[A/G]TGTGGTGGCTCACAC | 26094 |
rs565578738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944119 | GTGGGGTCTGGTGAT[C/G]CACAGGCCACTGTTC | 26094 |
rs565601312 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924714 | CTCCCATCTGTACCC[C/T]CCTTCCATCCTGGCT | 26094 |
rs565758532 | snp | C/T | 3.30737e-05 | 0.00406642 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945854 | AGGCGCAGCCTGGGA[C/T]GTCACCCACTGCCCC | 26094 |
rs565758958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952433 | TCTCAGTCCACATCC[A/G]TGGAGAATTAGGTGA | 26094 |
rs565889945 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948539 | GGGCTAAAGAGGCCA[A/G]GCTCTGCAGAAAGCA | 26094 |
rs565953458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934229 | CGCTATCTCGGCTCA[C/T]GGCAACCTCCACCTC | 26094 |
rs565965915 | snp | A/T | 4.94181e-05 | 0.00497057 | stop-gained, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940252 | TTTGACCCTGAAAAG[A/T]AACGCTACTTCCGCT | 26094 |
rs566010418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947668 | TCCTGAGGCCAGGGA[C/G]GAAAACAGTGGTCAG | 26094 |
rs566097841 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960809 | GCTTTTCTTCACATA[A/C]ACAAGCAGATGGTGG | 26094 |
rs566104421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929764 | GTGACTCCATGGCGC[A/G]CAGCTCGTACGAAGC | 26094 |
rs566239295 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930353 | GGCTCACTGCAGCCT[C/G]CACCTCCCGGGTTCA | 26094 |
rs566363779 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924781 | AGGACTGTTGCTGCA[A/G]TAAGTTCCTTAGGGG | 26094 |
rs566438360 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940803 | ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 26094 |
rs566549070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950614 | GTCAGTCAAAAGACA[C/T]ACACGTAGGCAAGGG | 26094 |
rs566940766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938768 | TTAAATGGTATACCT[A/G]TGTATGACACTCCTG | 26094 |
rs566941910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953618 | GGGAGGCTGAGATGG[G/T]AGGATTCCTTGAGCC | 26094 |
rs567044595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932210 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 26094 |
rs567169634 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926321 | CCGAAGCCCCACTCC[C/T]CGCCTTCTTCATGAG | 26094 |
rs567181794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933149 | CAGCCTACCCCTCCT[A/T]CTCCCGAGCTGTGAC | 26094 |
rs567182078 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926121 | ACAGCGAGAGGACTT[C/G]TCCAGGGCCGCATCA | 26094 |
rs567231998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941514 | ATGTGGATGGGGAGC[A/G]TGGGCAGAGTTGACG | 26094 |
rs567403622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940768 | GCTAATTTTTTTATT[G/T]TTAGTAGAGACAGGG | 26094 |
rs567561750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929002 | AGGCCAGCCCCGATG[C/T]GTGCGGGCTGCCATC | 26094 |
rs567626857 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949575 | GCCTGGCCAACATGG[G/T]GAAACCCCATCTCTA | 26094 |
rs567781311 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72962000 | TCCCTCTGTTCTAAC[A/G]GCATCTCTTCCCTTC | 26094 |
rs567794541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955204 | ATGAACCCACTAACC[C/T]GCTTTTGGTGGAGAT | 26094 |
rs567831525 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931727 | TGTTGAATGTTTTTT[G/T]AATCATGAGAGGATG | 26094 |
rs567877939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955854 | CATGGGGACTGCTTC[A/G]TTGACCATATGAGCC | 26094 |
rs567935992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943721 | AGGTCCCTGACCTTT[C/T]GATGGACCACGTAAG | 26094 |
rs567957052 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951193 | GCTGTGTTTCCCAGG[A/C]TGGTCTCGAACTCCT | 26094 |
rs568078310 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925959 | GGCCCCCCGGTTTCA[C/T]GGTCAGGGCTCGCTA | 26094 |
rs568085633 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940193 | CACAGTGGTTGAAAT[C/T]GGTGCATTTAATTTT | 26094 |
rs568085797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933225 | AAATAATCCTTAAGA[A/G]GCACTGATCTACAAA | 26094 |
rs568187438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951269 | TACATAGGCAGGAGC[C/T]ACCACACCCAGCTTT | 26094 |
rs568196852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958439 | TCTTGTCATTGTTCT[A/G]GCACAACAGGGCGAC | 26094 |
rs568247028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946210 | AGCATAACATGCATG[A/G]TGAAACCTTGTCTCT | 26094 |
rs568446705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960226 | CAATGGCGCTCTCAC[C/T]GCACCCTCCACCTCC | 26094 |
rs568535543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72926964 | TGTGGTTGAAGCTTA[A/C]GAAGTGGCCGGCTCT | 26094 |
rs568593026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927602 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 26094 |
rs568850050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955987 | GAGTGCAGTGGTACT[A/G]TCTTGGCTTACTGCA | 26094 |
rs568853252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929603 | CAGGAAGAGGGCAGG[G/T]GAGGGGGCTCAGTCT | 26094 |
rs568912140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931806 | TGAGGTTTTCCCCAT[C/G]TATTAGTATGGTATA | 26094 |
rs569118122 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949745 | CTGAGCGAAAGAGCA[A/C]GACTCCATCTCAAAA | 26094 |
rs569168551 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961027 | TGAGCAGTTGGGCCC[A/C]CAGGTGTGCACCACC | 26094 |
rs569209028 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940496 | AGAGGCACTTCAGGG[A/G]GTGTGGCCCTAGCTT | 26094 |
rs569298063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943858 | GGTGGGACTGGAGGC[C/T]GATGCTAGAGATTGA | 26094 |
rs569318883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944151 | CAAGCCTGGACATCT[C/T]GACCCTCATGCTTCC | 26094 |
rs569445503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938300 | GTGAGGAGAGAGGAC[C/G]ACTCTCTGTTCTTTC | 26094 |
rs569449657 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956719 | GACAGCCTCATCCCA[-/C]TGTCAGTGGGCAAAC | 26094 |
rs569563333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72932131 | GTAGCTGAGACTACA[A/G]GTGTGCACCACCACG | 26094 |
rs569579336 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931351 | TAAATGTAACTTTTC[A/T]TTCATATTCAGGCTG | 26094 |
rs569689970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72953289 | ACAGGCGTGAGCCAC[C/T]ACGCCTGGCATGGAT | 26094 |
rs569748085 | snp | A/G | 0.000164715 | 0.0090736 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947137 | GCTGTGTGCTTCCTC[A/G]CCAGGTGAATTCGGT | 26094 |
rs569808885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946322 | AGGTGGGAAGATCAC[C/G]TGAGCCCAGGAGATC | 26094 |
rs569924113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927834 | GCTTGCGCCTGAAGT[A/T]TTTCTTAAATAAGTG | 26094 |
rs569936171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934777 | CGGTGCCTCCAAGCC[A/G]GGTAGCACAGCTTAT | 26094 |
rs569992577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942550 | TTCCTCCTTCTGAGA[C/T]AGAAAGTTAAAAATC | 26094 |
rs570198781 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960881 | GTCAGGCCCCCCCCA[A/C]CTTTTTTTTTTTTTG | 26094 |
rs570276693 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961539 | TTTTTCTCATTTCTC[A/G]TGGGAGAAAGGCAAG | 26094 |
rs570394032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945005 | GAGGTGGGAGAATAG[C/T]TTGAACCTGGGAGTC | 26094 |
rs570557811 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942506 | GCCAGAAACACCGTA[A/G]GTATCAGGCAGGGCA | 26094 |
rs570566867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957521 | GAAGCATTACTTTGT[C/T]AGGACATTCATAGAC | 26094 |
rs570577720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958184 | AGGCTGAGGCAGAAG[A/G]ATGGCTTGGGCCCAG | 26094 |
rs570617298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939724 | GCTGCAGAACTGCCC[A/G]AATGGACTCCCTGCC | 26094 |
rs570877717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948140 | ATCAGGATCTTTTTT[A/G]TAAATTTTATTTGTT | 26094 |
rs570913659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933179 | CAAACAAAAATGTCT[C/T]CAGACATTGCCAGAT | 26094 |
rs571039896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954614 | CATCAGAAAGGATCA[C/G]TGGGTTCCTTTGTAA | 26094 |
rs571052617 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926465 | CGCTACACCTTGGTC[G/T]TTCCGGGTCCTTGCA | 26094 |
rs571073234 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72926851 | GCGCTTCTCTGAGAC[C/T]TGCTGCTGAAGGCCC | 26094 |
rs571187171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941589 | TTGCCGAGGAAGGGA[G/T]ACTTGGAAAGGACAC | 26094 |
rs571245179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936133 | CGTGCTTCCCTTCCT[A/G]TGCGCAGTCCCTTTC | 26094 |
rs571260400 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937751 | GTGGGGTAGGAAACT[A/G]TGTGGTCGACTAAGG | 26094 |
rs571501556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955962 | GAGTCTTGCTCTGTC[A/G]CCCGGGCTGGAGTGC | 26094 |
rs571617973 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932265 | CAAAGTGCTGGGCTT[A/G]CAGGCGTGAGCCACT | 26094 |
rs571635159 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929159 | GCCTGCGCCTTGGGC[C/G]TATTGAGGCCAGGCC | 26094 |
rs571790785 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948008 | CTGGAAACAATGTGA[A/C]TACTCATTGTACCTC | 26094 |
rs571812693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949119 | CTTACTACCCAGAGC[C/G]GTATGTCACATACAC | 26094 |
rs571848257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937822 | GAGGCAGCCCTTCCC[A/G]GGTAAGGCTTGCTGT | 26094 |
rs571906226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950202 | GGGGGATAGACGGAC[A/G]AGAGCAAGTCCTCAG | 26094 |
rs571996555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926669 | GGCGGGGAGGGGCGG[A/G]GAGGAGTGAGCACGT | 26094 |
rs572024687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951333 | ACATCTGAAGCTGGC[C/T]AGTCACGATGGCTCA | 26094 |
rs572085271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939257 | TTCAGCCTATAATTC[C/T]CTCAGAAGCTACTTG | 26094 |
rs572099200 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947940 | GACTTGACTCACCCA[A/G]AACCACATGTTAATG | 26094 |
rs572210538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945434 | ATGCAGTCTTTTTCT[A/G]TTGCACGTTTTATTC | 26094 |
rs572252358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933490 | CTTGAACCCAGGAGG[A/C]AGAGGTTGCAGTGAG | 26094 |
rs572323637 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952778 | CAGCTCACCACAACC[C/T]CCGCCTCCCAGGTTC | 26094 |
rs572477385 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959911 | GCAAGAGGAGAGGGA[G/T]TGGTTCCCCGGCTCC | 26094 |
rs572520284 | snp | A/G | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962266 | GGAGCCACACTATTC[A/G]TCCTCAATAAAACAC | 26094 |
rs572626544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940851 | CTGCCTCAGCCTCCC[A/C]AAGTGCTGGGATTAC | 26094 |
rs572646961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958138 | AAAATTAGGCATGGC[A/G]GCACACACTTGTAGT | 26094 |
rs572676673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934447 | GTGTGAGCCACTGCA[C/T]CCGGCCTAATTTTTG | 26094 |
rs572717650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956252 | ATGAACAACAAGGCT[C/T]AAGAATTCGAGATGG | 26094 |
rs573095919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943329 | ACTTCAGCTCCGTCG[C/T]TTAACGTCAGAGTCT | 26094 |
rs573237417 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943006 | CAGTTTAGCCCACGA[A/G]CTGCGTCTCAGCTGC | 26094 |
rs573519299 | snp | A/C/T | 5.31574e-05 | 0.00515523 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940412 | GCCCCCTGTCCTCTC[A/C/T]GCTCCTGCCAGCACC | 26094 |
rs573579997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946458 | AAGAAAAGGACTCCA[A/G]GAGTTTCTTGTCTTG | 26094 |
rs573606545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939993 | AATTCCAGGAGCAAA[C/T]TGAAACACTCAGGGA | 26094 |
rs573639701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933897 | GGCTCCGCTATCCCA[A/G]GTACCATGTCCATAA | 26094 |
rs573764913 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927319 | ATTTTAAATAACGAT[A/G]GAAATTAGAGTCGCG | 26094 |
rs573847558 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939959 | AGGGAAGGCTGAGAC[C/G]CGTTCCTGGCTTGGA | 26094 |
rs573975930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947438 | TGATGTCACTGTGTG[G/T]CAGACACTGTCTGGG | 26094 |
rs574041231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936301 | GGGCTTGGTGGCCCA[C/T]GCCTGTAATCCCAGC | 26094 |
rs574044812 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925667 | TAGCCTCTGTGAATC[C/T]AGCTGTCCTCACAAA | 26094 |
rs574061467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72952273 | CTGGATATTACATTT[C/T]AGTCTATCAGAAAAT | 26094 |
rs574086281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947864 | CTTTGCTGAGAGCAC[A/G]GTAGTACAGTGTCGT | 26094 |
rs574089706 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960977 | CTGCAGTCTTGACCT[C/T]CTTGGGCTTGAGCAA | 26094 |
rs574091656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954097 | TATTTGGATGTTTTC[C/T]GAACCCAGTGGTCCC | 26094 |
rs574173478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941916 | CAGTCTGGATAGACC[A/G]TGTGGCTACCCCGTG | 26094 |
rs574381292 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930267 | TTTTTTGAGACGGAG[-/T]TTTTTTTTGTTTGTT | 26094 |
rs574385857 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927445 | CAGCCTCCGCCCCCG[A/G]GGTTCACGCCATTCT | 26094 |
rs574437424 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939113 | AATCCCAGCACTTTG[G/T]GAGACCAAGGCAGCC | 26094 |
rs574437695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72931748 | TGAGAGGATGTTGCA[C/T]TTTGTCCAGTGCTTT | 26094 |
rs574599456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72944629 | TAAACCCCGTCTCTA[A/C]AAAAAAATATAAATT | 26094 |
rs574629111 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925489 | TGAGAGCCAGGAGTT[C/T]AGCCTGAAATCCTAG | 26094 |
rs574701280 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959013 | TGAGAGAGCTTGGAA[G/T]TCCTTTTCATAAAAG | 26094 |
rs574747348 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926193 | TCCAGACAGTTCCGC[G/T]GCTCCGGGAGCAGCC | 26094 |
rs574751241 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941138 | CAGCTAATTTTTGTA[-/T]TTTTTTTTATAGAGA | 26094 |
rs574763557 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950284 | CAGGAGTGGAGGGAA[-/G]GGGCACCAAGAGGCA | 26094 |
rs575396073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954844 | CAGGCCAGGTACAGT[G/T]GCTAATGAATGGCTG | 26094 |
rs575407947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954642 | TAAGGGTGTCTGAGC[C/T]GAGTGAAAGTTGGTT | 26094 |
rs575667313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936488 | AGAATCGCTTGAACC[C/T]GAGAGGCAGAGGTTG | 26094 |
rs575728164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942810 | TTCATCTTCCTGAGC[A/G]TTCTGTGGGGAAACT | 26094 |
rs575900263 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924406 | GGTTGGAATGCCTCA[G/T]GACTTGCCCAAGGCC | 26094 |
rs575962599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951947 | TGGGGGTGGCTTAGA[A/G]AGAAGTATGGGGCCG | 26094 |
rs576066421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939460 | CTGCTGTTGTGCTGA[C/G]AAATGAGCCCAGCTG | 26094 |
rs576124516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934257 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 26094 |
rs576155378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926737 | CCGGCGCGCTCCGCC[A/C]GTTCTGGGGCGCGTG | 26094 |
rs576189234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941032 | GCAGTGGCGCCATCT[C/T]GGCTCACTGCAACCT | 26094 |
rs576262912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72927210 | CCATGGTGTTCTACA[A/G]GCATTGTCTTGTGAC | 26094 |
rs576310923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72935606 | TACTTGAGGTTGGCA[C/G]GCTCCCTTACCAGAT | 26094 |
rs576315864 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945198 | AGAAGTTCAAGACCA[A/G]CCTGGACAACATAGC | 26094 |
rs576368165 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930098 | ATCGCGCCACTGCAC[C/T]TCAGCCAAAAGGGGG | 26094 |
rs576374272 | snp | A/G | 8.24627e-05 | 0.00642063 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941732 | ATTGTTCTCTTTTTT[A/G]TAATAAATATAGATT | 26094 |
rs576557313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72949412 | AGTGAGCTGTGATCA[C/T]ACTACTGCACTCCAG | 26094 |
rs576582558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947305 | AGGACTAGACCCTTG[C/T]GCACTTACATCTCAC | 26094 |
rs576583823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943942 | CCTTCCATGTAAGGG[A/G]TGTTGGGGACCGGGC | 26094 |
rs576642355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72950083 | TGTCTCTGGCTAGGG[A/G]GCAGGGCCTTTCAAG | 26094 |
rs576658099 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72928117 | TAGAAGCTACTTTGT[A/C]TTCAGCTTTACAGAC | 26094 |
rs576707871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938492 | ATACACTCATGCTTC[A/G]CTTAACAAGGAGGAA | 26094 |
rs576752792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956379 | GCCCCTGGTGCTTTT[C/T]CCACAGATCAAGCTG | 26094 |
rs576763354 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962281 | ATCCTCAATAAAACA[C/T]TTCCCCAGCTATCAG | 26094 |
rs576813356 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957294 | AGATTAGGAGCAGCT[A/G]TCTGGCCACTAAGCC | 26094 |
rs577043714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72930760 | TTTATAGTTTTAGAT[C/T]GAGATCCATTTTGGT | 26094 |
rs577235668 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926279 | CTCCACGTGCATCCG[C/T]CCCAGACAGGCCAGG | 26094 |
rs577287808 | in-del | -/CAAGAATAAGAACAGC | 0.00119737 | 0.0244387 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940531 | CTGACAGGAAGAAGA[-/CAAGAATAAGAACAGC]CAAGAGCCCCCTTCT | 26094 |
rs577329911 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932908 | TTTCTTTCTTTTTTT[C/T]AATGTTGTTTGTTTG | 26094 |
rs577375368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72957832 | TCCAGTAGTGTATAT[C/T]ATGTTTCTGGGCTGC | 26094 |
rs577412451 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927998 | GCGGAGGGGTGTCTC[A/G]CTATGTTGCCCAGGC | 26094 |
rs577500602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951410 | TGAGGTCGGGTGTTC[A/G]AGACGAGTCTGACCA | 26094 |
rs577752478 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961078 | TTTTTGTAGAGATGG[C/T]GTCTCCCTATGTTTC | 26094 |
rs577771188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72960464 | CCGATTCTTAAATAT[A/G]TTTAATCCGTCCGCC | 26094 |
rs577981713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955353 | CTAGCCACTAACAAG[C/G]AATCATCCTCCCTTC | 26094 |
rs578019169 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936444 | TGGCAGGTGCCTGTA[G/T]TCCCAGCTACTCGGG | 26094 |
rs578034886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF4 | GRCh38.p7 | 14:72948445 | GTTCTCTAAATTGCA[A/C]ATTTTATGTGGCTTT | 26094 |
rs578042846 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949927 | CCACAAGTCCTCAGT[A/G]TAGGAGGAAAGCTGC | 26094 |
rs578085496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72929292 | TTTGTGTGGAAAACT[A/G]CTAGACTGTGAGAGA | 26094 |
rs745335354 | in-del | -/TTTTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927345 | TCGCGGTGGTGTTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs745345828 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955417 | GTGTCTAATCACACC[A/G]TCTGACCCAGAGGCT | 26094 |
rs745369414 | snp | C/T | 4.94197e-05 | 0.00497066 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945919 | GCTCTTCACAGTGAA[C/T]GATGTTAAAGTTGGA | 26094 |
rs745389800 | in-del | -/CTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942123 | TAGAAGCTCCTACAA[-/CTT]CATTCCCATGACATT | 26094 |
rs745422403 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | DCAF4 | GRCh38.p7 | 14:72946022 | CTCTACTTCACCAAC[C/T]GGAAGGTACGTTGCC | 26094 |
rs745453198 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955591 | GCGTTGTGGAAATCA[A/G]GGCAAGGGATGGAAG | 26094 |
rs745558813 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929700 | CGGATGTGCGTCCCC[A/G]CCCTTTTCTTGATGA | 26094 |
rs745611810 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931186 | TCAATCTGTAATTTC[C/T]TTCAACAGTGTTTTA | 26094 |
rs745672293 | snp | A/G | 1.65231e-05 | 0.00287424 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940362 | GCTGCTCCAGGAAGA[A/G]GACAGACGGAAAAAG | 26094 |
rs745750640 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951880 | AATAGTCACCCAGGT[A/G]CAGGGTTCTCCTCCT | 26094 |
rs745775732 | in-del | -/TTTTTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927344 | GTCGCGGTGGTGTTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs745795968 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948605 | ACAGCATGGTATTCT[C/T]GTTTCTGTGGGCTAA | 26094 |
rs745835278 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950538 | AAGGCAAGGGAATGA[C/G]AATAAATACAGGCTC | 26094 |
rs745888525 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939744 | GACTCCCTGCCCCCG[C/T]CAGAATGGCTGGAAC | 26094 |
rs746082515 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934735 | TGCAGGGGTTGGTCT[C/G]TGCATCTGTCTCCCA | 26094 |
rs746146902 | snp | A/G | 1.7879e-05 | 0.00298985 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956427 | GAAGTGCGTAAGGCA[A/G]TACGAAGGCCACGTG | 26094 |
rs746170915 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956257 | CAACAAGGCTCAAGA[A/T]TTCGAGATGGAGATC | 26094 |
rs746172868 | in-del | -/GATCTTTGCAGATCTTTGCAG | 1.65081e-05 | 0.00287293 | cds-indel | DCAF4 | GRCh38.p7 | 14:72955558 | TGCCGCTCTGGGGAA[-/GATCTTTGCAGATCTTTGCAG]ATCTTTGCCATTGAT | 26094 |
rs746199185 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945524 | ACTAGCATTTTTCCT[A/G]TTGCGCCACAGCCTT | 26094 |
rs746220622 | in-del | -/TTTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927344 | GTCGCGGTGGTGTTC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs746221653 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941863 | GTTTTCTTCATGAAT[A/G]TTCTTTTCCTGTTTC | 26094 |
rs746276548 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943032 | GCTGCATGGAGAGGA[A/G]AAAGGTCCAGATTCG | 26094 |
rs746320393 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954379 | AGCCCATCTCTGTCT[C/T]CGCCAGGCTTGTCTC | 26094 |
rs746450387 | in-del | -/C | 1.64732e-05 | 0.0028699 | frameshift-variant, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940236 | GCTACCTGGGTTTTA[-/C]TTTGACCCTGAAAAG | 26094 |
rs746498247 | snp | A/G | 5.16302e-05 | 0.0050806 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955486 | CCTCAGAGGGATGTC[A/G]TGATAGCCAGGCACT | 26094 |
rs746549714 | snp | G/T | 1.66043e-05 | 0.00288129 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943123 | GGGGACACCTGCCTA[G/T]GGTGTGGCTGCCACC | 26094 |
rs746651864 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953316 | GGATTGTTTTATTTC[C/T]TAACCTGGGTGGTGG | 26094 |
rs746769933 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942913 | GATGGGCGTCAGCGG[A/G]GCAGGGAAGGCCAGA | 26094 |
rs746826984 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929567 | TTTTATTTTATTTTT[C/T]CGTCAAGCTGTTCTT | 26094 |
rs746831850 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931133 | TGCTTTTCCATTGCT[-/A]AAAAAAATGGCATTT | 26094 |
rs746838937 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940281 | CTTGCTCCCTGGACA[C/T]AACAACTGCAACCCC | 26094 |
rs747126068 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950437 | CTGGAATGTTTCCAT[A/C]AGATTTAGAAACCAG | 26094 |
rs747195359 | snp | G/T | 1.64844e-05 | 0.00287087 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941847 | AATGCCTCTTTGTTA[G/T]GTTTTCTTCATGAAT | 26094 |
rs747290907 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952352 | AGGCAGACCTGGCAC[G/T]AATCCCAGCTCTGCC | 26094 |
rs747303108 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939282 | TACTTGTGGATTTAC[A/G]AATCAAGTGTTTTAG | 26094 |
rs747347568 | snp | C/T | 1.81783e-05 | 0.00301477 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958781 | GGCTGTCGGGCAGGA[C/T]CTTTACTGTTACTCC | 26094 |
rs747354067 | snp | A/G/T | 3.29464e-05 | 0.00405861 | missense | DCAF4 | GRCh38.p7 | 14:72954230 | CCTGTGCCTGGTCCC[A/G/T]GAATATCCAAGCAAA | 26094 |
rs747363831 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941737 | TCTCTTTTTTGTAAT[A/G]AATATAGATTGCCAG | 26094 |
rs747409051 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954347 | TCTCCCCAGACTACA[C/T]GTGACATAATCTTAC | 26094 |
rs747414264 | snp | C/T | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961760 | ATGCAGTGACTACAC[C/T]TGGTTGGCATCCCAT | 26094 |
rs747451689 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941451 | GCAGACCTGTTTGCA[A/G]TCCCATTGCTGCACT | 26094 |
rs747505284 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957736 | ATAGCACTTCTGGTC[G/T]TAGAGCCACACAAGT | 26094 |
rs747560478 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945459 | TTATTCAATGCAATT[G/T]TTTTTTCATGGTGGT | 26094 |
rs747618277 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939428 | CAATAAAGAATGAAA[C/T]TCACCTAGCCTTGTA | 26094 |
rs747694345 | snp | C/T | 2.66265e-05 | 0.00364864 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939892 | CACAGCTGGGACCTC[C/T]TCTGTGCCAGGTAAG | 26094 |
rs747729160 | in-del | -/AG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930740 | CTTTGTTTCCTTCAA[-/AG]AGTTTTATAGTTTTA | 26094 |
rs747802518 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951997 | GGATTCCCTAAGCCT[A/G]TCCCAGGGTTAGTAC | 26094 |
rs747946755 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946045 | ACGTTGCCCATCCCT[A/G]TAGCCTCTCTGCACA | 26094 |
rs747983403 | snp | C/T | 6.58892e-05 | 0.00573936 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947138 | CTGTGTGCTTCCTCA[C/T]CAGGTGAATTCGGTG | 26094 |
rs747991917 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941643 | TTCTGCCAATTTAGT[A/G]CCTGTTTCCTTCATT | 26094 |
rs748004346 | snp | A/T | 8.03487e-05 | 0.00633781 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939834 | CACAGCCCGCTCACG[A/T]TTCCGGCCACGGTGA | 26094 |
rs748036552 | snp | C/T | 1.72877e-05 | 0.00293999 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955733 | CAGGCCACAGGGTCT[C/T]GTGGCCCAGTGCCCT | 26094 |
rs748103065 | snp | A/G | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959091 | CCCTGCCTTTTCTTA[A/G]CAAAAAGGACTTTTC | 26094 |
rs748158030 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960052 | CTGGTCATCACACCT[C/T]ACTGTTGCTGGCCCA | 26094 |
rs748167200 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927488 | TCCCGCGTAGCTGGG[A/G]CTACAGGCGACCACC | 26094 |
rs748215992 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941815 | TTCTCAACGTCACCA[A/T]TTACTGCCAGTAAGA | 26094 |
rs748241590 | snp | A/C | 1.64999e-05 | 0.00287222 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941725 | TCATTGAATTGTTCT[A/C]TTTTTTGTAATAAAT | 26094 |
rs748333256 | snp | A/G | 1.6473e-05 | 0.00286988 | stop-gained | DCAF4 | GRCh38.p7 | 14:72954213 | GATCCCTGGTGCCTG[A/G]TCCTGTGCCTGGTCC | 26094 |
rs748370356 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950091 | GCTAGGGAGCAGGGC[C/G]TTTCAAGACTGAATG | 26094 |
rs748479610 | snp | A/G | 1.65669e-05 | 0.00287805 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951929 | TGTCTCCCGAGAGCT[A/G]TGTGGGGGTGGCTTA | 26094 |
rs748527133 | in-del | -/CT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954694 | GTTGCTCTACACAAC[-/CT]CTCATGGAAAGGTAT | 26094 |
rs748557733 | snp | C/T | 1.6727e-05 | 0.00289193 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958721 | TCCCAGTGTGGCCTT[C/T]TCGTCGCGGCTGGGG | 26094 |
rs748579913 | in-del | -/TGGT | 1.65051e-05 | 0.00287267 | intron-variant, frameshift-variant | DCAF4 | GRCh38.p7 | 14:72954481 | AGCAGTTTGCTCTCA[-/TGGT]TGGTTGGTTGGATTG | 26094 |
rs748595467 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945903 | ATACCAACAGTGACC[A/G]GCTCTTCACAGTGAA | 26094 |
rs748630115 | snp | A/G | 1.85824e-05 | 0.00304809 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937947 | ACACAGAGATGTATG[A/G]ATTTTTTTGTTTTTC | 26094 |
rs748736400 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956949 | CCGGCGCGGTGGCTC[A/G]CGCCCGTAATCCCAA | 26094 |
rs748756541 | in-del | -/CT | 3.46386e-05 | 0.0041615 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940402 | TCACCCCTTCGCCCC[-/CT]GTCCTCTCCGCTCCT | 26094 |
rs748806231 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931495 | TAGGATTTTCTGTAT[A/G]TAAGATCATGTTTGG | 26094 |
rs748837905 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928284 | CCGCAACCTCCGCCT[C/T]CCAGGTTTAAGGGAT | 26094 |
rs748881245 | snp | A/C/G/T | 9.82189e-05 | 0.00700729 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939881 | ACCTCGTCTGGCACA[A/C/G/T]CTGGGACCTCCTCTG | 26094 |
rs748933426 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956734 | ATGTCAGTGGGCAAA[C/T]GTCACTTCAGAAACA | 26094 |
rs749004525 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932991 | CAATCCTCCTGCCTC[A/G]GCTTCCCGAGCAGCT | 26094 |
rs749021832 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950612 | GCGTCAGTCAAAAGA[C/G]ACACACGTAGGCAAG | 26094 |
rs749040132 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930324 | CCAGGCTGCAATGCA[-/G]GTGGCACCATCTCGG | 26094 |
rs749058655 | snp | A/C | 0.000131833 | 0.00811782 | missense | DCAF4 | GRCh38.p7 | 14:72955610 | AAGGGATGGAAGGCC[A/C]CCCGCCTGTTTCATG | 26094 |
rs749102464 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928509 | AGTCTACAGACTCTT[-/A]ACAAAATTCCCCTGT | 26094 |
rs749114895 | snp | A/G | 1.69198e-05 | 0.00290854 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955707 | GAAAGGTAGGGGATC[A/G]TGGACTTTCTCAGGC | 26094 |
rs749248122 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949602 | TCTACTAAAAATACA[A/G]AAATTAGCCAGGTGT | 26094 |
rs749276863 | snp | C/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925773 | CTGGGACAGGCACAG[C/G]ACACATAGGTCATTC | 26094 |
rs749358785 | snp | C/T | 1.65321e-05 | 0.00287502 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951912 | TAAAGAAATCTGTCC[C/T]CTGTCTCCCGAGAGC | 26094 |
rs749413805 | snp | A/G | 9.94926e-05 | 0.0070524 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940370 | AGGAAGAAGACAGAC[A/G]GAAAAAGGTGGGCTC | 26094 |
rs749414744 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72935962 | TTCCTATCAGTCTTT[-/TT]CTCTTTTTGAGATGG | 26094 |
rs749589532 | in-del | -/CACAGG | 1.69178e-05 | 0.00290837 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955517 | AGCAGTCCCTCTTTC[-/CACAGG]CACAGGCTCCTCTGC | 26094 |
rs749627923 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936676 | GTTAGAGAGAAATCA[C/T]GAACTCACTTTTGAA | 26094 |
rs749673409 | in-del | -/AATA | 4.94735e-05 | 0.00497336 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941734 | TGTTCTCTTTTTTGT[-/AATA]AATATAGATTGCCAG | 26094 |
rs749686707 | snp | C/G | 1.67967e-05 | 0.00289794 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954522 | AATATAAAAGTTTGC[C/G]CCATGTAGAAATTTG | 26094 |
rs749708574 | snp | C/T | 9.43583e-05 | 0.00686806 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937933 | AAGCCCATGCCCACA[C/T]ACAGAGATGTATGGA | 26094 |
rs749748418 | snp | C/T | 1.648e-05 | 0.0028705 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943038 | TGGAGAGGAAAAAGG[C/T]CCAGATTCGAAGCAT | 26094 |
rs749777308 | in-del | -/AG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954586 | CTAGTACTCTTTGAC[-/AG]GGGAGAAAGAGCATC | 26094 |
rs749875563 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938816 | ACTGGAAGTCAGTGA[A/G]TGAGTGATGAGTGAA | 26094 |
rs749944047 | snp | G/T | 0.000219422 | 0.010472 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955703 | GCTGGAAAGGTAGGG[G/T]ATCATGGACTTTCTC | 26094 |
rs749949094 | snp | A/G | 2.15371e-05 | 0.00328148 | missense | DCAF4 | GRCh38.p7 | 14:72956390 | TTTTTCCACAGATCA[A/G]GCTGTGGGACCTGAG | 26094 |
rs750035558 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925378 | TCAAGGCCGCTCAAG[C/T]TTCATGAAGCGGTTC | 26094 |
rs750056575 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941802 | AGCCAGCTGGGTTTT[A/C]TCAACGTCACCAATT | 26094 |
rs750072519 | in-del | -/CTGAAGACAGGCAAGTGTGCCG | 1.64727e-05 | 0.00286986 | frameshift-variant, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938060 | TCAGACTCCGTGATT[-/CTGAAGACAGGCAAGTGTGCCG]CTGAAGACAGGCAAG | 26094 |
rs750084617 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952914 | TGGTTAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 26094 |
rs750128107 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957639 | GCTGGATGATAGAGA[C/G]AGCTCAGCCTTGCTG | 26094 |
rs750197043 | in-del | -/GTT | 1.9418e-05 | 0.00311587 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946077 | TTGACCCTGGGGGTA[-/GTT]GGCCAAATTCAGGGT | 26094 |
rs750217137 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | DCAF4 | GRCh38.p7 | 14:72954188 | GGCCTGGCATGCTCT[A/G]CAGTTTCCGGATCCC | 26094 |
rs750223050 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932882 | CTGAATAATTTTTTT[G/T]TCTTTCTTTCTTTCT | 26094 |
rs750237205 | snp | C/G | 1.86813e-05 | 0.00305619 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940429 | CTCCTGCCAGCACCT[C/G]TCCATCCACTGTTGA | 26094 |
rs750259033 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960576 | GGCTGACAGTCTTCT[C/G]TATTCTCTTTCCCAC | 26094 |
rs750290820 | snp | A/G | 1.6513e-05 | 0.00287336 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958689 | CCCTCCCCGTACCCT[A/G]CCTCCAAGGCCGACA | 26094 |
rs750523062 | snp | A/T | 1.65187e-05 | 0.00287386 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958605 | ATGTGTCTCTCCTCT[A/T]TCCTAGTGGGCCAGG | 26094 |
rs750585266 | in-del | -/T/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940588 | TTCTTGTTCGATAAG[-/T/TT]TTGTTTTTTTTTTTT | 26094 |
rs750628491 | snp | A/G | 0.000115774 | 0.00760748 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943104 | TCATACTGGTGAGTG[A/G]GAGGGGGACACCTGC | 26094 |
rs750842181 | snp | G/T | 1.6681e-05 | 0.00288794 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954511 | GGGACAGGCAGAATA[G/T]AAAAGTTTGCCCCAT | 26094 |
rs750942030 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940316 | CGAAAGAGAGCATCC[A/G]GCAGAAGGAGATGGA | 26094 |
rs750983329 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948628 | TGGGCTAAGGAGAGG[A/G]AAAAAAAATCCATGT | 26094 |
rs751039870 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947320 | TGCACTTACATCTCA[C/T]GCTTTAGAAAAAAAA | 26094 |
rs751093095 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936315 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGACG | 26094 |
rs751175811 | snp | A/G | 9.8837e-05 | 0.00702914 | missense | DCAF4 | GRCh38.p7 | 14:72954173 | TAGCAGGAATAGACC[A/G]GCCTGGCATGCTCTG | 26094 |
rs751202229 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949111 | ATTTGGAGCTTACTA[-/C]CCAGAGCGGTATGTC | 26094 |
rs751225785 | in-del | -/T | 1.66852e-05 | 0.0028883 | frameshift-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72958718 | ATTCCCAGTGTGGCC[-/T]TTCTCGTCGCGGCTG | 26094 |
rs751311450 | in-del | -/CTGTGCCACC | 3.29625e-05 | 0.00405958 | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72951831 | CGCAGAGACTCCAGG[-/CTGTGCCACC]CTGCTCCCAGCATCA | 26094 |
rs751313780 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938691 | GCAGTCAGTACACAG[A/T]GGTATTTGTGTATCT | 26094 |
rs751319272 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943779 | CTTCCTGGAGGCTGA[A/G]GGAAAGCCAGGGAGA | 26094 |
rs751349997 | snp | C/T | 1.64996e-05 | 0.0028722 | missense | DCAF4 | GRCh38.p7 | 14:72951871 | CTGTTCGTCAATAGT[C/T]ACCCAGGTACAGGGT | 26094 |
rs751363335 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957531 | TTTGTTAGGACATTC[A/G]TAGACTTATTTACTA | 26094 |
rs751424307 | in-del | -/TG | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951678 | AACGCATGTTGAATC[-/TG]GACGGTGGGGGTTAC | 26094 |
rs751470383 | snp | C/T | 5.06513e-05 | 0.0050322 | missense, utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72937994 | ATGAATAAAAGTCGC[C/T]GGCAGAGTAGAAGAC | 26094 |
rs751509495 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931095 | GGGTATTCTGGGTCC[C/T]TTGCATAATATGAAT | 26094 |
rs751574775 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944826 | AGGTGTGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 26094 |
rs751589114 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947820 | CTCATCACACTAGTC[C/T]CTGCCTTCCCGGAGA | 26094 |
rs751686234 | snp | C/G | 1.65866e-05 | 0.00287976 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954497 | TGGTTGGTTGGATTG[C/G]GACAGGCAGAATATA | 26094 |
rs751709816 | snp | C/T | 1.65149e-05 | 0.00287353 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943094 | CGATTTAACCTCATA[C/T]TGGTGAGTGGGAGGG | 26094 |
rs751954274 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925508 | CTGAAATCCTAGCTT[C/T]CTGGTTAAGAGCTGA | 26094 |
rs751963920 | snp | C/T | 4.94189e-05 | 0.00497062 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947121 | AATAACTTTCCATCT[C/T]GCTGTGTGCTTCCTC | 26094 |
rs751983056 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940197 | GTGGTTGAAATTGGT[A/G]CATTTAATTTTTTTG | 26094 |
rs752065571 | snp | G/T | 4.52683e-05 | 0.00475732 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939869 | GAGTCTCCGTCAACC[G/T]CGTCTGGCACAGCTG | 26094 |
rs752114098 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947231 | TTGGTGGGCAGGCCA[C/T]ACCCTGACGTTGGAC | 26094 |
rs752182696 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933497 | CCAGGAGGCAGAGGT[C/T]GCAGTGAGCCGAGAT | 26094 |
rs752197789 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935551 | TGAGCCACCACATCC[A/G]GCCTTTAAAATGATT | 26094 |
rs752206794 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946164 | GACTTGATTTTTTAC[G/T]TGAGCCTAGGAGTTT | 26094 |
rs752208876 | snp | G/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959542 | GGCCCGGCGTCAAAG[G/T]AAATTGGTTTTGACT | 26094 |
rs752209911 | in-del | -/ACAGCCCAGA | 1.86399e-05 | 0.0030528 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958817 | CTAATTCTGCAGGGC[-/ACAGCCCAGA]GCCATGTGGATTTGA | 26094 |
rs752235122 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957585 | CCTCCTTTTTAAGTC[A/G]ATTTTTCACCTGTTT | 26094 |
rs752242788 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940260 | TGAAAAGAAACGCTA[C/T]TTCCGCTTGCTCCCT | 26094 |
rs752249688 | snp | A/G | 6.59652e-05 | 0.00574267 | missense | DCAF4 | GRCh38.p7 | 14:72951862 | CCAGCATCACTGTTC[A/G]TCAATAGTCACCCAG | 26094 |
rs752304788 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940335 | GAAGGAGATGGAGAG[C/G]AAGAGACTGCGGCTG | 26094 |
rs752330283 | snp | C/T | 1.66219e-05 | 0.00288283 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958573 | AGTTTTCCTTTGCAT[C/T]CTCTCACTAGCCTGC | 26094 |
rs752460715 | snp | A/G | 1.90561e-05 | 0.0030867 | missense | DCAF4 | GRCh38.p7 | 14:72956470 | TACCTGCCCCTGCAT[A/G]TGCACGAGGAAGAAG | 26094 |
rs752579554 | snp | A/C | 1.64958e-05 | 0.00287187 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943085 | GCAAGCGACCGATTT[A/C]ACCTCATACTGGTGA | 26094 |
rs752703997 | snp | C/G | 0.000346178 | 0.0131518 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954336 | GTAGTTGTCCCTCTC[C/G]CCAGACTACATGTGA | 26094 |
rs752749307 | snp | A/G | 8.72239e-05 | 0.00660336 | missense | DCAF4 | GRCh38.p7 | 14:72956389 | CTTTTTCCACAGATC[A/G]AGCTGTGGGACCTGA | 26094 |
rs752762600 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941387 | TCAAGGTAGGCAATG[A/G]AATGTAAAGTTCCAG | 26094 |
rs752804514 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943739 | TGGACCACGTAAGAG[C/T]AGGGCCTGCCCGGCA | 26094 |
rs752858878 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930782 | CATTTTGGTTCATTT[C/T]TGTCCCATATGGTAT | 26094 |
rs752860092 | snp | A/G | 4.94849e-05 | 0.00497393 | missense | DCAF4 | GRCh38.p7 | 14:72954400 | GGCTTGTCTCGGCGG[A/G]TCCTGTTGACCAACG | 26094 |
rs752903248 | snp | A/C | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961468 | TTTGTACCATTTGGT[A/C]CAATTGATCTTGATC | 26094 |
rs752910029 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932365 | CTTATAAAATGATTC[A/G]GAAAAATGTAGTAAA | 26094 |
rs752947265 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927949 | GCATGCACCACCACA[C/T]CCGGCTAATTTTTAA | 26094 |
rs752968124 | in-del | ATATATATATATA/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[ATATATATATATA/T]TATATATATATATAT | 26094 |
rs753054832 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | DCAF4 | GRCh38.p7 | 14:72946001 | AAGGTGTTCATGCAC[A/G]AAAACCTCTACTTCA | 26094 |
rs753064885 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951141 | ACACACCACCACGCC[C/T]AGCTAGTTTTTGTAT | 26094 |
rs753109951 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947096 | TCCACAGGAAAGCAT[A/G]TTACTGTAGAATAAC | 26094 |
rs753136564 | snp | A/G | 1.67214e-05 | 0.00289144 | missense | DCAF4 | GRCh38.p7 | 14:72955688 | ATGGCTTCAGACATG[A/G]CTGGAAAGGTAGGGG | 26094 |
rs753246065 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929305 | CTGCTAGACTGTGAG[A/G]GAGAGCCGACCTCCT | 26094 |
rs753258158 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925401 | AGCGGTTCTTTATTC[C/T]GACTATGCCCACTTC | 26094 |
rs753309587 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924387 | TAATCTGTGAAGAAA[C/T]TGAGGTTGGAATGCC | 26094 |
rs753319362 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953060 | GGCTGGAGTGCAATG[A/T]CACGATCTCAGTTCA | 26094 |
rs753336892 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929824 | GCTACAAACTTGGTG[C/T]GTTTGCTCAGACGCC | 26094 |
rs753341756 | snp | C/T | 3.29478e-05 | 0.00405867 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947239 | CAGGCCACACCCTGA[C/T]GTTGGACCTGGGTAT | 26094 |
rs753368375 | snp | G/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924544 | TGGACATTCAACAGA[G/T]CCTGCTGGCCGGCTG | 26094 |
rs753389134 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947130 | CCATCTCGCTGTGTG[A/C]TTCCTCACCAGGTGA | 26094 |
rs753471389 | snp | G/T | 1.91573e-05 | 0.00309488 | missense | DCAF4 | GRCh38.p7 | 14:72956406 | GCTGTGGGACCTGAG[G/T]ACCACGAAGTGCGTA | 26094 |
rs753712853 | snp | A/C | 3.29609e-05 | 0.00405948 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954302 | AGAGAAGAGGCCTTA[A/C]CAGGCCTTAAAACCC | 26094 |
rs753902392 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961333 | CTGCTGTGTCCTGCT[C/T]ATTTTCCAGGCCCAG | 26094 |
rs753916676 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941590 | TGCCGAGGAAGGGAG[A/G]CTTGGAAAGGACACC | 26094 |
rs753955361 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | DCAF4 | GRCh38.p7 | 14:72945995 | ACGCTCAAGGTGTTC[A/G]TGCACGAAAACCTCT | 26094 |
rs753968395 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942625 | TCCTGGGGCTCTTCC[C/T]GGCAGCCGTATCCTG | 26094 |
rs754063009 | snp | C/G | 1.67391e-05 | 0.00289297 | missense, synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938039 | AGCCACCAGCAGAAC[C/G]CTTGGTTCAGACTCC | 26094 |
rs754159294 | snp | A/G | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961375 | TGGGAAAGAGTTGAG[A/G]GATACTTTTCTAACA | 26094 |
rs754214409 | snp | G/T | | | downstream-variant-500B | DCAF4 | GRCh38.p7 | 14:72962328 | GAGCTGGCTACTGTT[G/T]CCATCAAGAACAGAG | 26094 |
rs754229381 | snp | A/G | 1.65172e-05 | 0.00287373 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955555 | TGGCTGCCGCTCTGG[A/G]GAAATCTTTGCCATT | 26094 |
rs754243465 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948671 | AGGGATGGATGGTCT[A/G]TTGTAGCTTCATCAG | 26094 |
rs754259813 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946568 | GGTCCAGGAGTTGAT[C/G]TGGAAGGGCCCACAC | 26094 |
rs754264390 | snp | C/T | 4.94686e-05 | 0.00497311 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945875 | CCACTGCCCCCTTCC[C/T]TTCTCCAGGCAGATA | 26094 |
rs754369146 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949962 | AGGAGGGATTGCAGC[C/T]ACCTTCCTGGAGGGA | 26094 |
rs754438252 | in-del | -/T | 1.65045e-05 | 0.00287263 | splice-donor-variant | DCAF4 | GRCh38.p7 | 14:72951877 | TCAATAGTCACCCAG[-/T]GTACAGGGTTCTCCT | 26094 |
rs754517055 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929848 | AGACGCCCGCGGCGG[C/T]GGCTGTGCCTGGGCT | 26094 |
rs754527096 | in-del | -/TTT | 1.6473e-05 | 0.00286988 | cds-indel, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940264 | AGAAACGCTACTTCC[-/TTT]GCTTGCTCCCTGGAC | 26094 |
rs754572386 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945300 | CAGGAGGCTGAGGAG[A/G]GAAGATCACTTGAGC | 26094 |
rs754594205 | snp | C/T | 0.000148769 | 0.00862336 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958700 | CCCTGCCTCCAAGGC[C/T]GACATTCCCAGTGTG | 26094 |
rs754612235 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934599 | CGGGCTTGCCTGACA[G/T]TTTCATTCTTCAGAC | 26094 |
rs754648909 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947131 | CATCTCGCTGTGTGC[C/T]TCCTCACCAGGTGAA | 26094 |
rs754739797 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935889 | GCACTCTAAAGAAAT[G/T]TTGACCTTTTTATAG | 26094 |
rs754829401 | snp | C/G/T | 5.61554e-05 | 0.00529859 | missense | DCAF4 | GRCh38.p7 | 14:72956411 | GGGACCTGAGGACCA[C/G/T]GAAGTGCGTAAGGCA | 26094 |
rs754976946 | snp | C/T | 0.000103441 | 0.00719096 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958753 | GCTCCCGGGGCGCGC[C/T]GGGGCTGCTCATGGC | 26094 |
rs754993892 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941592 | CCGAGGAAGGGAGAC[G/T]TGGAAAGGACACCGT | 26094 |
rs755032980 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | DCAF4 | GRCh38.p7 | 14:72954205 | AGTTTCCGGATCCCT[A/G]GTGCCTGGTCCTGTG | 26094 |
rs755048951 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942627 | CTGGGGCTCTTCCCG[C/G]CAGCCGTATCCTGGG | 26094 |
rs755052056 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941713 | ACAAATAAATCTTCA[C/T]TGAATTGTTCTCTTT | 26094 |
rs755102270 | in-del | -/CA | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961605 | CCAGCACAAACCATT[-/CA]CAGTCTTCCCGCAAT | 26094 |
rs755197024 | snp | C/T | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961383 | AGTTGAGAGATACTT[C/T]TCTAACAGGGTAAAC | 26094 |
rs755255070 | snp | A/G | 0.000115394 | 0.00759499 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72945884 | CCTTCCCTTCTCCAG[A/G]CAGATACCAACAGTG | 26094 |
rs755294704 | snp | G/T | 6.50512e-05 | 0.00570275 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939752 | GCCCCCGTCAGAATG[G/T]CTGGAACTCAAGTCC | 26094 |
rs755355096 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948806 | GGTACTTTGTTCAGA[C/T]CTGCACTCTGCATTT | 26094 |
rs755366587 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949009 | TCTTCACTTCCTTGC[C/T]TTCCAAACCCAGAAG | 26094 |
rs755444687 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950136 | TGGGAGGTCCCAGGG[C/G]GTTGTGATTGTGGAG | 26094 |
rs755469319 | snp | A/G | 5.16889e-05 | 0.00508348 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955478 | CTGCCCAGCCTCAGA[A/G]GGATGTCATGATAGC | 26094 |
rs755541492 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | DCAF4 | GRCh38.p7 | 14:72946023 | TCTACTTCACCAACC[A/G]GAAGGTACGTTGCCC | 26094 |
rs755580043 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924355 | AACCTTTCTCAGTAG[A/G]TGTCTTATCCTCATT | 26094 |
rs755599726 | snp | C/G | 0.000148357 | 0.00861141 | missense | DCAF4 | GRCh38.p7 | 14:72956392 | TTTCCACAGATCAAG[C/G]TGTGGGACCTGAGGA | 26094 |
rs755635989 | snp | C/G | 2.0773e-05 | 0.00322274 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939818 | TCTGACTCCCGGGCA[C/G]CACAGCCCGCTCACG | 26094 |
rs755683830 | in-del | -/CT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954558 | ATTGAAATTGGACTC[-/CT]CTGTGTGCCATCTAG | 26094 |
rs755696670 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957640 | CTGGATGATAGAGAG[A/C]GCTCAGCCTTGCTGA | 26094 |
rs755761714 | snp | A/G | 1.68915e-05 | 0.00290611 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955704 | CTGGAAAGGTAGGGG[A/G]TCATGGACTTTCTCA | 26094 |
rs755795454 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945021 | TTGAACCTGGGAGTC[A/G]GAGATTTCAGCAAGC | 26094 |
rs755866038 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938148 | ATGTCACACGATCAC[A/C]GGTGTGGAGATCACC | 26094 |
rs755879173 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928139 | TTTACAGACCAGTGG[A/C]GTTAGCGTTTTGCAC | 26094 |
rs755886528 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941805 | CAGCTGGGTTTTCTC[A/G]ACGTCACCAATTACT | 26094 |
rs755911081 | snp | C/T | 1.65304e-05 | 0.00287488 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941695 | ATTCTCCATCATCCC[C/T]TAACAAATAAATCTT | 26094 |
rs756104899 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954192 | TGGCATGCTCTGCAG[C/T]TTCCGGATCCCTGGT | 26094 |
rs756138456 | in-del | -/AGCC | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927557 | GGGTTTCACCGTGTT[-/AGCC]AGCCAGGATGGTCTC | 26094 |
rs756196929 | snp | C/T | 6.60491e-05 | 0.00574632 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958691 | CTCCCCGTACCCTGC[C/T]TCCAAGGCCGACATT | 26094 |
rs756310145 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936671 | CGGGGGTTAGAGAGA[A/G]ATCATGAACTCACTT | 26094 |
rs756328538 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941549 | GACTTTCCCACTCAC[A/T]CTTTCTTCTGCTGGG | 26094 |
rs756363847 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929099 | GGGGCTGCTCCCTAC[G/T]GGGTGTAGCGCACCC | 26094 |
rs756367598 | snp | A/G/T | 5.61319e-05 | 0.00529744 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958830 | GCACAGCCCAGAGCC[A/G/T]TGTGGATTTGACTTA | 26094 |
rs756475141 | snp | A/C | 1.65004e-05 | 0.00287227 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945867 | GACGTCACCCACTGC[A/C]CCCTTCCCTTCTCCA | 26094 |
rs756498755 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959963 | GCTGTAACCAAAACC[C/T]ACCACTTCTATTGGA | 26094 |
rs756523503 | in-del | -/TT/TTT | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934156 | TTACGTGGCATTTTC[-/TT/TTT]TTTTTTTTTTTTTTG | 26094 |
rs756563176 | snp | A/G | 1.6544e-05 | 0.00287606 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943106 | ATACTGGTGAGTGGG[A/G]GGGGGACACCTGCCT | 26094 |
rs756594173 | in-del | -/C | 1.67726e-05 | 0.00289586 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954521 | GAATATAAAAGTTTG[-/C]CCCATGTAGAAATTT | 26094 |
rs756662721 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946203 | CTGGGCAGCATAACA[-/T]TGCATGGTGAAACCT | 26094 |
rs756672597 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948651 | ATCCATGTAATTGGA[C/G]TTAAAGGGATGGATG | 26094 |
rs756696836 | snp | G/T | 1.64857e-05 | 0.00287099 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954432 | GGTGACGGGACACCG[G/T]CAGTCCTTTGGGACC | 26094 |
rs756718673 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936364 | AAGCCAGGAGTTCTT[A/G]AGCAGCCTGGCCAAC | 26094 |
rs756764514 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945917 | CGGCTCTTCACAGTG[A/G]ACGATGTTAAAGTTG | 26094 |
rs756769433 | snp | C/T | 3.35289e-05 | 0.0040943 | missense, synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938054 | CCTTGGTTCAGACTC[C/T]GTGATTCTGAAGACA | 26094 |
rs756774486 | snp | A/G | 0.000251836 | 0.0112185 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955693 | TTCAGACATGGCTGG[A/G]AAGGTAGGGGATCAT | 26094 |
rs756885170 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955316 | TGCTACCCATGAGGA[A/G]GACACATGGGGTCTG | 26094 |
rs756924795 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950917 | GAGAAGAGCAGTTCT[C/T]TCTGAGTAGAGGAGA | 26094 |
rs757038655 | snp | C/G | 3.30085e-05 | 0.00406241 | missense | DCAF4 | GRCh38.p7 | 14:72951877 | GTCAATAGTCACCCA[C/G]GTACAGGGTTCTCCT | 26094 |
rs757090548 | snp | A/C/G | 3.30198e-05 | 0.00406313 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940359 | GCGGCTGCTCCAGGA[A/C/G]GAAGACAGACGGAAA | 26094 |
rs757129813 | snp | C/G | 2.09888e-05 | 0.00323944 | missense | DCAF4 | GRCh38.p7 | 14:72956485 | GTGCACGAGGAAGAA[C/G]GAATCCTGGTGGCAG | 26094 |
rs757152724 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944900 | TCGAGACCAGCCTGA[A/C]CAACATTGTGAAACC | 26094 |
rs757189324 | snp | A/T | 8.24165e-05 | 0.00641883 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951750 | AATGTCCATGCCTCC[A/T]CCCAGAGGGGAGCCT | 26094 |
rs757196225 | in-del | -/TTTTTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927346 | CGCGGTGGTGTTCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 26094 |
rs757215242 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931164 | GGAATTTTGATAGGG[A/C]TTGCATTCAATCTGT | 26094 |
rs757381812 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943095 | GATTTAACCTCATAC[C/T]GGTGAGTGGGAGGGG | 26094 |
rs757446239 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955994 | GTGGTACTATCTTGG[C/T]TTACTGCAACCTCTG | 26094 |
rs757481271 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954320 | GGCCTTAAAACCCCA[C/T]GTAGTTGTCCCTCTC | 26094 |
rs757551290 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925526 | GGTTAAGAGCTGAAA[C/T]GCCTTCGCACGGCGT | 26094 |
rs757824645 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941469 | CCATTGCTGCACTCA[C/T]GCACCTGGTGGCTTC | 26094 |
rs757832863 | snp | C/T | 3.6485e-05 | 0.00427097 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958785 | GTCGGGCAGGACCTT[C/T]ACTGTTACTCCTACA | 26094 |
rs757950361 | snp | A/G | 3.29663e-05 | 0.00405981 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940344 | GGAGAGCAAGAGACT[A/G]CGGCTGCTCCAGGAA | 26094 |
rs758174459 | snp | C/G/T | 7.80996e-05 | 0.00624857 | missense, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956475 | GCCCCTGCATGTGCA[C/G/T]GAGGAAGAAGGAATC | 26094 |
rs758175576 | in-del | -/GCTCACGATTCCG | 2.03382e-05 | 0.00318884 | frameshift-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939826 | CGGGCAGCACAGCCC[-/GCTCACGATTCCG]GCTCACGATTCCGGC | 26094 |
rs758178761 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953261 | CGCTTCGGCCTCCTA[A/T]AGTGCTGGGATTACA | 26094 |
rs758181303 | snp | A/C | 1.64933e-05 | 0.00287165 | missense | DCAF4 | GRCh38.p7 | 14:72951865 | GCATCACTGTTCGTC[A/C]ATAGTCACCCAGGTA | 26094 |
rs758181662 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940265 | AGAAACGCTACTTCC[A/G]CTTGCTCCCTGGACA | 26094 |
rs758241136 | snp | A/G | | | missense | DCAF4 | GRCh38.p7 | 14:72956435 | TAAGGCAGTACGAAG[A/G]CCACGTGAATGAGTA | 26094 |
rs758269437 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947243 | CCACACCCTGACGTT[C/G]GACCTGGGTATCTGT | 26094 |
rs758269538 | in-del | -/TG | 1.64787e-05 | 0.00287038 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951776 | AGCCTTGTGCCTAAC[-/TG]TCCTTAACAGCTTTT | 26094 |
rs758290434 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943751 | GAGCAGGGCCTGCCC[A/G]GCAAGCCCTATCCTT | 26094 |
rs758310641 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930861 | CCAGCAGTTGAAAAG[A/G]CACTTCTTTCTTTCA | 26094 |
rs758319103 | snp | A/G | 1.82937e-05 | 0.00302432 | missense | DCAF4 | GRCh38.p7 | 14:72956417 | TGAGGACCACGAAGT[A/G]CGTAAGGCAGTACGA | 26094 |
rs758329549 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942830 | GTGGGGAAACTCAAA[G/T]TCGGATAATCTGGGA | 26094 |
rs758368196 | snp | G/T | 0.00104704 | 0.0228566 | missense | DCAF4 | GRCh38.p7 | 14:72954401 | GCTTGTCTCGGCGGG[G/T]CCTGTTGACCAACGT | 26094 |
rs758407563 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941416 | AGCCCTGGGTCACCA[C/T]GGGTGGAATGGAGAG | 26094 |
rs758464874 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941831 | TTACTGCCAGTAAGA[C/T]AATGCCTCTTTGTTA | 26094 |
rs758474543 | snp | G/T | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961504 | CATTTTTTCCACATG[G/T]GTCAGAGACAAGGGT | 26094 |
rs758486673 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930786 | TTGGTTCATTTTTGT[C/T]CCATATGGTATGAAG | 26094 |
rs758652612 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950350 | GAAGGCCAGGATAGA[C/T]CTCCCAGAGAGTGGT | 26094 |
rs758694378 | snp | A/G | 4.94539e-05 | 0.00497238 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954339 | GTTGTCCCTCTCCCC[A/G]GACTACATGTGACAT | 26094 |
rs758696428 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929848 | GACGCCCGCGGCGGC[-/G]GGCTGTGCCTGGGCT | 26094 |
rs758707671 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939165 | TTGAGACCAGTCTGG[C/G]CAACACGGCGAAACT | 26094 |
rs758785720 | snp | C/T | 2.20534e-05 | 0.00332057 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939861 | GTGATGACGAGTCTC[C/T]GTCAACCTCGTCTGG | 26094 |
rs758961199 | snp | C/G | 1.64806e-05 | 0.00287054 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72946009 | CATGCACGAAAACCT[C/G]TACTTCACCAACCGG | 26094 |
rs758977963 | snp | A/G | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961715 | GCTCAGGACATTTGA[A/G]GATTGCGTGTTTGGC | 26094 |
rs758996389 | snp | A/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925445 | ATCACCCGGCCCCGC[A/T]CCACATACTGCATTT | 26094 |
rs759008234 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942013 | AAAGCTGTTCTCTCT[A/C]GAGCGAAGGCGGGGG | 26094 |
rs759071079 | snp | A/G | 5.40877e-05 | 0.00520009 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956556 | CTGTCTCTCAGGGGC[A/G]ATCCCAGCAACTTCA | 26094 |
rs759121980 | in-del | -/TTCA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930097 | ATCGCGCCACTGCAC[-/TTCA]TTCAGCCAAAAGGGG | 26094 |
rs759218445 | snp | A/G | 3.29712e-05 | 0.00406011 | intron-variant, missense | DCAF4 | GRCh38.p7 | 14:72954467 | GTGATGTCTTGGCCC[A/G]GCAGTTTGCTCTCAT | 26094 |
rs759235473 | snp | A/G | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959435 | CTAGAAGTTTTAAAC[A/G]GTCCTTAACATGCCT | 26094 |
rs759281290 | in-del | -/GCTGGGGGGCT | 3.36545e-05 | 0.00410196 | frameshift-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72958729 | GGCCTTCTCGTCGCG[-/GCTGGGGGGCT]GCTGGGGGGCTCCCG | 26094 |
rs759286648 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960463 | CCCGATTCTTAAATA[C/T]ATTTAATCCGTCCGC | 26094 |
rs759292437 | snp | A/C | 1.66123e-05 | 0.00288199 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942980 | ATCCATGCCCCCACC[A/C]TCTGTTTCTGCAGTT | 26094 |
rs759347791 | snp | A/G | 0.000346155 | 0.0131513 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943074 | CCTCCGCCTTGGCAA[A/G]CGACCGATTTAACCT | 26094 |
rs759510779 | snp | A/G | 6.10706e-05 | 0.00552554 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939845 | CACGATTCCGGCCAC[A/G]GTGATGACGAGTCTC | 26094 |
rs759555907 | in-del | -/A | 1.65411e-05 | 0.00287581 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943106 | ATACTGGTGAGTGGG[-/A]GGGGGACACCTGCCT | 26094 |
rs759559029 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938314 | CCACTCTCTGTTCTT[C/T]CCTAAGTGACCACGA | 26094 |
rs759573395 | snp | C/T | 6.61627e-05 | 0.00575126 | missense | DCAF4 | GRCh38.p7 | 14:72954397 | CCAGGCTTGTCTCGG[C/T]GGGTCCTGTTGACCA | 26094 |
rs759609626 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945513 | ATGTAATAGGAACTA[A/G]CATTTTTCCTATTGC | 26094 |
rs759628824 | in-del | -/TA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930643 | GTATGTGTGTGTGTA[-/TA]TATATATATATGTAG | 26094 |
rs759638745 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | DCAF4 | GRCh38.p7 | 14:72947178 | TCGCTGAATCACTTG[A/G]ATTCCCACATTCTGT | 26094 |
rs759691749 | snp | C/T | 4.38953e-05 | 0.00468462 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939929 | TGCGGGGTGGGAATC[C/T]TGGCCCTTGCACACA | 26094 |
rs759743168 | snp | C/T | 1.96988e-05 | 0.00313831 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946078 | TGACCCTGGGGGTAG[C/T]TGGCCAAATTCAGGG | 26094 |
rs759836991 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943623 | TGGTTTGGGTTGGAC[A/C]CAAGCTGGAAGCCAA | 26094 |
rs759890375 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930623 | GATGAAGCCCAATTT[A/T]TGTGTGTATGTGTGT | 26094 |
rs759899579 | snp | A/T | 3.25346e-05 | 0.00403314 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956361 | CCTGGCCCCTCCCTG[A/T]TGGCCCCTGGTGCTT | 26094 |
rs759943449 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932073 | GGCTCACTGCAACCT[C/T]TGCCTCCCAGGTTCA | 26094 |
rs760039912 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940029 | CTGGGTGCGTCAGGA[A/G]TGGTGGTCATGAGGC | 26094 |
rs760054034 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941771 | GGGATTTAATGCATC[C/T]TCCATGCTACGAAAA | 26094 |
rs760105259 | snp | A/G | 1.80536e-05 | 0.00300441 | missense | DCAF4 | GRCh38.p7 | 14:72956452 | CACGTGAATGAGTAC[A/G]CCTACCTGCCCCTGC | 26094 |
rs760113865 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952144 | CAGATTCGGACGCCC[A/G]TGCACATCATTCAGA | 26094 |
rs760151102 | snp | C/G | 3.29598e-05 | 0.00405941 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943060 | TCGAAGCATGGATCC[C/G]TCCGCCTTGGCAAGC | 26094 |
rs760215278 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946227 | AAACCTTGTCTCTAC[-/A]AAAAAAAAAAAAAAA | 26094 |
rs760234320 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925385 | CGCTCAAGCTTCATG[A/G]AGCGGTTCTTTATTC | 26094 |
rs760365835 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941110 | CTGGGATTACAGGAA[C/G]CTGCCACCATGCCCA | 26094 |
rs760404123 | snp | C/T | 1.65097e-05 | 0.00287308 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945863 | CTGGGACGTCACCCA[C/T]TGCCCCCTTCCCTTC | 26094 |
rs760416730 | snp | C/T | 1.87531e-05 | 0.00306206 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958842 | GCCATGTGGATTTGA[C/T]TTACGGGAGTAAAGC | 26094 |
rs760439729 | snp | A/G | 1.69358e-05 | 0.00290992 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942969 | TCAGCTTCAGCATCC[A/G]TGCCCCCACCCTCTG | 26094 |
rs760522622 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947127 | TTTCCATCTCGCTGT[G/T]TGCTTCCTCACCAGG | 26094 |
rs760618140 | snp | A/C | 2.01574e-05 | 0.00317464 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939841 | CGCTCACGATTCCGG[A/C]CACGGTGATGACGAG | 26094 |
rs760651691 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935698 | CAGTGATTTTATCAT[C/T]GGCTGCGTCCTGCTG | 26094 |
rs760694836 | in-del | -/TAGGGGA | 1.68172e-05 | 0.00289971 | splice-donor-variant | DCAF4 | GRCh38.p7 | 14:72955698 | ACATGGCTGGAAAGG[-/TAGGGGA]TCATGGACTTTCTCA | 26094 |
rs760790013 | snp | A/C | 1.75585e-05 | 0.00296293 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955747 | TCGTGGCCCAGTGCC[A/C]TGCCAGGTGAAAGGG | 26094 |
rs760825876 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942365 | GGAACTGTCTGACTC[C/T]AACACCTGAGCGCCC | 26094 |
rs760998531 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956030 | CAGGTTCAAGCGATT[C/G]TCCTGCCTCAGCCTC | 26094 |
rs761092339 | in-del | -/CCTGCCAGTAC | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960111 | CCCACTTGAATGTTT[-/CCTGCCAGTAC]CCTGCCAGTACCCTG | 26094 |
rs761101704 | snp | A/G | 1.65674e-05 | 0.00287809 | missense | DCAF4 | GRCh38.p7 | 14:72955548 | TGTTTAATGGCTGCC[A/G]CTCTGGGGAAATCTT | 26094 |
rs761218360 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961002 | GAGCAATCCTCCCAC[C/G]TCAGTCTTCTGAGCA | 26094 |
rs761226651 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930102 | CGCCACTGCACTTCA[A/G]CCAAAAGGGGGGTAG | 26094 |
rs761329508 | snp | C/T | 3.29881e-05 | 0.00406115 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954122 | GGTCCCTGGCCTGCC[C/T]AGAAGGCAGCCACAC | 26094 |
rs761365401 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941789 | CATGCTACGAAAAAG[C/T]CAGCTGGGTTTTCTC | 26094 |
rs761522771 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950756 | TACCCATTCAGATAA[C/G]CAGAAATTTTAAGGG | 26094 |
rs761552600 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938701 | CACAGTGGTATTTGT[C/G]TATCTCAACATAGAA | 26094 |
rs761600006 | snp | C/G | 5.0929e-05 | 0.00504598 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958735 | TCTCGTCGCGGCTGG[C/G]GGGCTCCCGGGGCGC | 26094 |
rs761704558 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958493 | TCCGTTAATGAGTTT[A/G]TGTTTTGGCTCACAT | 26094 |
rs761757510 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945745 | AAGTGAGGTCATCTC[C/T]ACTCTCGCTCATGGA | 26094 |
rs761779574 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945929 | GTGAACGATGTTAAA[A/G]TTGGAGGCTCCAAGT | 26094 |
rs761854002 | in-del | -/GGGT | 1.67312e-05 | 0.00289229 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946072 | CACACTTGACCCTGG[-/GGGT]AGTTGGCCAAATTCA | 26094 |
rs761924009 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935534 | TGTTGGGATTACAGG[C/T]GTGAGCCACCACATC | 26094 |
rs761953600 | snp | C/G | 0.000155972 | 0.0088296 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940402 | TCACCCCTTCGCCCC[C/G]TGTCCTCTCCGCTCC | 26094 |
rs761955373 | snp | A/G | 1.66283e-05 | 0.00288338 | missense | DCAF4 | GRCh38.p7 | 14:72955541 | CCTCTGCTGTTTAAT[A/G]GCTGCCGCTCTGGGG | 26094 |
rs761966935 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952369 | ATCCCAGCTCTGCCC[C/T]TTGCCAACTTGAATG | 26094 |
rs762047938 | in-del | -/TT | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959678 | ACTTCTGTGAATGAC[-/TT]AGGAGATCATGAGCT | 26094 |
rs762097752 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957043 | TGGTGAAACCCCATC[G/T]CTACTAAAATACAAA | 26094 |
rs762110456 | in-del | -/CCCTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945868 | ACGTCACCCACTGCC[-/CCCTT]CCCTTCTCCAGGCAG | 26094 |
rs762176585 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954296 | GTGCCCAGAGAAGAG[A/G]CCTTAACAGGCCTTA | 26094 |
rs762199428 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940309 | CCCCTGACGAAAGAG[A/G]GCATCCGGCAGAAGG | 26094 |
rs762219421 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | DCAF4 | GRCh38.p7 | 14:72951810 | CAGGCTATGCCTCAT[A/G]GGACTCGCAGAGACT | 26094 |
rs762316487 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960952 | GTTGCAGTAGCACAA[C/T]TACTACTCACTGCAG | 26094 |
rs762375531 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935566 | GGCCTTTAAAATGAT[C/T]TTTGCTTGACCTTGC | 26094 |
rs762376672 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942094 | TATTCTCTGTTACTC[A/G]TAAGTCATTCTAGTA | 26094 |
rs762408052 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929843 | TGCTCAGACGCCCGC[A/G]GCGGCGGCTGTGCCT | 26094 |
rs762521351 | snp | A/G | 3.29478e-05 | 0.00405867 | missense | DCAF4 | GRCh38.p7 | 14:72954166 | ATCCCCTTAGCAGGA[A/G]TAGACCGGCCTGGCA | 26094 |
rs762573869 | snp | C/T | 1.79419e-05 | 0.0029951 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940414 | CCCCTGTCCTCTCCG[C/T]TCCTGCCAGCACCTG | 26094 |
rs762574209 | snp | A/T | 1.64738e-05 | 0.00286995 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954261 | TAACTGCTTCAGTAC[A/T]GGTGAGCCTGGCTCC | 26094 |
rs762635079 | snp | C/G | 1.6546e-05 | 0.00287624 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945842 | AGGCAGTCCACCAGG[C/G]GCAGCCTGGGACGTC | 26094 |
rs762671448 | snp | A/C | 1.65787e-05 | 0.00287907 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958582 | TTGCATTCTCTCACT[A/C]GCCTGCCATGTGTCT | 26094 |
rs762691854 | snp | C/T | 1.69315e-05 | 0.00290955 | missense, utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72937991 | GAAATGAATAAAAGT[C/T]GCTGGCAGAGTAGAA | 26094 |
rs762714872 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949717 | AGCCAAGATTGCGCC[A/C]CTGCACTCCAGCCTG | 26094 |
rs762824569 | in-del | -/G | 1.66358e-05 | 0.00288402 | intron-variant | DCAF4 | GRCh38.p7 | 14:72958569 | GGTAAGTTTTCCTTT[-/G]CATTCTCTCACTAGC | 26094 |
rs762828244 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957636 | TGAGCTGGATGATAG[A/G]GAGAGCTCAGCCTTG | 26094 |
rs762833259 | in-del | -/TT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940591 | TTGTTCGATAAGTTG[-/TT]TTTTTTTTTTTTTTT | 26094 |
rs762843910 | in-del | -/TGTTCTTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927339 | TTAGAGTCGCGGTGG[-/TGTTCTTTT]TTTTTTTTTTTTTTT | 26094 |
rs762943527 | in-del | -/TGATCCTTTGTACCATTTGGTCCAAT | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961447 | ACTCCTCTACTCACA[-/TGATCCTTTGTACCATTTGGTCCAAT]TGATCTTGATCTCAT | 26094 |
rs762957390 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958341 | GCACTTGAACGTTCC[A/G]TGACATCAAGAGCAG | 26094 |
rs762972296 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957357 | GATGGTGGCTATAGC[A/G]TAATCAGACAGTGTG | 26094 |
rs762986330 | snp | C/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924940 | TTCTTGAGACAGGGT[C/G]TCACTCTGTCACCCA | 26094 |
rs763015152 | snp | C/T | 1.65038e-05 | 0.00287257 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943088 | AGCGACCGATTTAAC[C/T]TCATACTGGTGAGTG | 26094 |
rs763046868 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945725 | TGGCTGCACTAAGTT[G/T]GGGAAAGTGAGGTCA | 26094 |
rs763052231 | snp | C/T | 1.69761e-05 | 0.00291337 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955512 | GCACTGAGCAGTCCC[C/T]CTTTCCACAGGCTCC | 26094 |
rs763075323 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945626 | TCATGCAGACCTCAG[A/G]CTTTCTGGCCATGTC | 26094 |
rs763108340 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant, missense | DCAF4 | GRCh38.p7 | 14:72954483 | GCAGTTTGCTCTCAT[A/G]GTTGGTTGGATTGGG | 26094 |
rs763255947 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932428 | CAGAAGGAAGGCATG[C/T]ACATTTGTAAGTTAC | 26094 |
rs763273520 | snp | G/T | 1.64735e-05 | 0.00286993 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947113 | TACTGTAGAATAACT[G/T]TCCATCTCGCTGTGT | 26094 |
rs763418039 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952889 | TAGTAGAGACGGGAT[G/T]TCACCATGTTGGTTA | 26094 |
rs763429476 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929308 | CTAGACTGTGAGAGA[C/G]AGCCGACCTCCTCAT | 26094 |
rs763437388 | snp | C/T | 2.3517e-05 | 0.00342898 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956383 | CTGGTGCTTTTTCCA[C/T]AGATCAAGCTGTGGG | 26094 |
rs763462444 | in-del | -/ATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928589 | GTAAACATCCTTTAT[-/ATATATATA]TATATATATATATAT | 26094 |
rs763484047 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932384 | AAATGTAGTAAATAT[C/T]TTGGAATCATTTTTG | 26094 |
rs763501274 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941278 | CCCAGCTGTCTATTT[C/T]AAATAGAAGACCAGG | 26094 |
rs763642317 | snp | C/T | 3.63537e-05 | 0.00426328 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940416 | CCTGTCCTCTCCGCT[C/T]CTGCCAGCACCTGTC | 26094 |
rs763649887 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960974 | TCACTGCAGTCTTGA[C/G]CTCCTTGGGCTTGAG | 26094 |
rs763685990 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | DCAF4 | GRCh38.p7 | 14:72954172 | TTAGCAGGAATAGAC[C/T]GGCCTGGCATGCTCT | 26094 |
rs763741630 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945505 | TAGTGCCTATGTAAT[A/G]GGAACTAGCATTTTT | 26094 |
rs763797722 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949848 | TCCAGTGAGGAATAT[A/G]TGTGGTCATTCAGAC | 26094 |
rs763904252 | snp | A/G | 1.69115e-05 | 0.00290782 | missense, utr-variant-5-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72937992 | AAATGAATAAAAGTC[A/G]CTGGCAGAGTAGAAG | 26094 |
rs763927482 | snp | C/T | 1.65072e-05 | 0.00287286 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943090 | CGACCGATTTAACCT[C/T]ATACTGGTGAGTGGG | 26094 |
rs763928317 | snp | A/G | 5.95918e-05 | 0.00545824 | missense | DCAF4 | GRCh38.p7 | 14:72956476 | CCCCTGCATGTGCAC[A/G]AGGAAGAAGGAATCC | 26094 |
rs763986380 | in-del | -/A | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954586 | CTAGTACTCTTTGAC[-/A]GGGGAGAAAGAGCAT | 26094 |
rs764036364 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957647 | ATAGAGAGAGCTCAG[C/G]CTTGCTGAGAGGCAG | 26094 |
rs764050403 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943269 | CTACCCGCTGGGAGA[C/T]GCTGAGCTGGCAGGC | 26094 |
rs764053455 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943767 | GCAAGCCCTATCCTT[A/C]CTGGAGGCTGAGGGA | 26094 |
rs764115251 | snp | C/T | 1.67711e-05 | 0.00289573 | missense | DCAF4 | GRCh38.p7 | 14:72955526 | CTCTTTCCACAGGCT[C/T]CTCTGCTGTTTAATG | 26094 |
rs764148823 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932677 | CAGCAAATTGTTTTC[A/G]AGTGCTTCCTACATA | 26094 |
rs764203214 | snp | C/T | 3.31203e-05 | 0.00406928 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954494 | TCATGGTTGGTTGGA[C/T]TGGGACAGGCAGAAT | 26094 |
rs764386488 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947222 | GGAAGAGGTTTGGTG[C/G]GCAGGCCACACCCTG | 26094 |
rs764410576 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952222 | TAACAGTCTGCCTAC[A/G]TTAAGGCAATTTGAC | 26094 |
rs764482723 | snp | C/T | | | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940288 | CCTGGACATAACAAC[C/T]GCAACCCCCTGACGA | 26094 |
rs764510222 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951176 | TGTAGAGACAAGGTT[A/T]TGCTGTGTTTCCCAG | 26094 |
rs764529230 | snp | C/T | 8.89355e-05 | 0.00666782 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956439 | GCAGTACGAAGGCCA[C/T]GTGAATGAGTACGCC | 26094 |
rs764537599 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941354 | ACCAACAGGTCTAGA[C/T]GCTAACATATTTTGT | 26094 |
rs764589127 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926459 | GGCTGACGCTACACC[C/T]TGGTCTTTCCGGGTC | 26094 |
rs764619408 | snp | C/T | 0.000164723 | 0.00907383 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947114 | ACTGTAGAATAACTT[C/T]CCATCTCGCTGTGTG | 26094 |
rs764769542 | snp | G/T | 1.64833e-05 | 0.00287078 | missense | DCAF4 | GRCh38.p7 | 14:72951835 | GAGACTCCAGGCTGT[G/T]CCACCCTGCTCCCAG | 26094 |
rs764787093 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928100 | GCCACCGCCCTGGCC[C/T]GTAGAAGCTACTTTG | 26094 |
rs764834943 | snp | A/T | | | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958714 | CCGACATTCCCAGTG[A/T]GGCCTTCTCGTCGCG | 26094 |
rs764890039 | snp | A/G | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959524 | TTGAATGTCAGATTC[A/G]AGGGCCCGGCGTCAA | 26094 |
rs764952635 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943075 | CTCCGCCTTGGCAAG[C/T]GACCGATTTAACCTC | 26094 |
rs765000092 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948417 | AATTTATATAAGGCA[C/T]CAAACTATGTGTGTT | 26094 |
rs765034139 | in-del | -/ACAAAAAA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946226 | TGAAACCTTGTCTCT[-/ACAAAAAA]AAAAAAAAAAAATTA | 26094 |
rs765060789 | snp | A/G | 3.30677e-05 | 0.00406605 | missense | DCAF4 | GRCh38.p7 | 14:72954398 | CAGGCTTGTCTCGGC[A/G]GGTCCTGTTGACCAA | 26094 |
rs765146992 | in-del | -/G | 1.67716e-05 | 0.00289578 | frameshift-variant, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938015 | AGTAGAAGACGACAT[-/G]GGAGAAGAAGCCACC | 26094 |
rs765157077 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954987 | AGGCATAGTGCTGGG[C/T]GCCTGTAATCCCAGC | 26094 |
rs765183449 | snp | G/T | 1.65507e-05 | 0.00287664 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939930 | GCGGGGTGGGAATCC[G/T]GGCCCTTGCACACAG | 26094 |
rs765218098 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956260 | CAAGGCTCAAGAATT[C/T]GAGATGGAGATCTTC | 26094 |
rs765431926 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947094 | ATTCCACAGGAAAGC[A/G]TATTACTGTAGAATA | 26094 |
rs765451488 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943639 | CAAGCTGGAAGCCAA[A/G]GTCAGCCGCTTAAAC | 26094 |
rs765507568 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944756 | ATGATTGTGCCACCA[C/G]ACTCCAGCCTGGGCA | 26094 |
rs765509782 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930672 | AGTGTGTGTGAGTTT[G/T]GGGTGTCATATTTGA | 26094 |
rs765528699 | snp | C/G | 2.88122e-05 | 0.00379543 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956370 | TCCCTGATGGCCCCT[C/G]GTGCTTTTTCCACAG | 26094 |
rs765562699 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932278 | TTACAGGCGTGAGCC[A/T]CTGCACCCGGCCTTG | 26094 |
rs765565292 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931516 | TCATGTTTGGTTGCC[-/T]TTTCTTTGTCTTGCC | 26094 |
rs765619908 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938883 | ACTTTAAAACCCTGT[A/G]CACCAGGCTACATTA | 26094 |
rs765696012 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951138 | GGCACACACCACCAC[A/G]CCCAGCTAGTTTTTG | 26094 |
rs765765812 | snp | A/G | 1.65203e-05 | 0.002874 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955663 | GATCCTCCAAGATGA[A/G]CAATACCTGATGGCT | 26094 |
rs765791089 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940049 | GGTCATGAGGCAAAC[C/T]GCCTCCCCCAGGACT | 26094 |
rs765837559 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941776 | TTAATGCATCTTCCA[A/T]GCTACGAAAAAGCCA | 26094 |
rs765969034 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955221 | CTTTTGGTGGAGATG[A/G]AATGCTATCTCTGGG | 26094 |
rs765999458 | snp | C/G | 0.00018543 | 0.00962708 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942973 | CTTCAGCATCCATGC[C/G]CCCACCCTCTGTTTC | 26094 |
rs766067484 | in-del | -/TCCAGGCTATGCCTCATGGGACTCGCAGAGAC | 1.6477e-05 | 0.00287024 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951793 | TCCTTAACAGCTTTT[lengthTooLong]TCCAGGCTGTGCCAC | 26094 |
rs766107642 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941806 | AGCTGGGTTTTCTCA[A/G]CGTCACCAATTACTG | 26094 |
rs766157382 | snp | G/T | 2.06956e-05 | 0.00321673 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956394 | TCCACAGATCAAGCT[G/T]TGGGACCTGAGGACC | 26094 |
rs766185026 | snp | G/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959394 | TATCCAAAGGCGTTG[G/T]AAGGAAAGATGGATC | 26094 |
rs766259136 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935761 | GAGTGGGACACAGTC[C/G]TGCCTCCTGTGGGTG | 26094 |
rs766340018 | in-del | -/CCATACCCTCC | 1.64909e-05 | 0.00287144 | frameshift-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72958669 | CCCGCCTACTGAGAA[-/CCATACCCTCC]CCGTACCCTGCCTCC | 26094 |
rs766369125 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942812 | CATCTTCCTGAGCGT[A/T]CTGTGGGGAAACTCA | 26094 |
rs766375341 | snp | C/T | 1.87704e-05 | 0.00306347 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958846 | TGTGGATTTGACTTA[C/T]GGGAGTAAAGCGTAA | 26094 |
rs766376690 | in-del | -/C | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933440 | GGCATGCGCCTGTAG[-/C]CCCAGCTATTCGGGA | 26094 |
rs766415529 | snp | C/T | 2.02022e-05 | 0.00317816 | missense, synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939842 | GCTCACGATTCCGGC[C/T]ACGGTGATGACGAGT | 26094 |
rs766485294 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945873 | ACCCACTGCCCCCTT[C/T]CCTTCTCCAGGCAGA | 26094 |
rs766596013 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | DCAF4 | GRCh38.p7 | 14:72955646 | GCAGTGACCTCTGTG[C/T]GGATCCTCCAAGATG | 26094 |
rs766615022 | snp | C/T | 3.32138e-05 | 0.00407502 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954500 | TTGGTTGGATTGGGA[C/T]AGGCAGAATATAAAA | 26094 |
rs766634930 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929128 | CCCGCCCCCCACCCC[A/G]CCCGGCCTCCTCTGG | 26094 |
rs766653249 | snp | C/G | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945985 | GAAGACCCCTACGCT[C/G]AAGGTGTTCATGCAC | 26094 |
rs766665898 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942573 | TAAAAATCTAGTTAG[A/T]TCTGTTCCTCACCCT | 26094 |
rs766666363 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956204 | GGGATTACAGGCATG[A/G]GCCACCGTGCCCGGC | 26094 |
rs766719236 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943398 | AACTTCTCCTTGGCT[C/G]TGTTGTATATGCAAT | 26094 |
rs766721178 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961299 | GCTCTTCCCAACTCT[G/T]AAGCCCCTGTTCCCC | 26094 |
rs766724522 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948658 | TAATTGGACTTAAAG[A/G]GATGGATGGTCTGTT | 26094 |
rs766750331 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961290 | TAAGATTCCGCTCTT[C/T]CCAACTCTGAAGCCC | 26094 |
rs766801657 | snp | C/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926162 | GGAGGAAGACACGGT[C/G]TCTCACGAAAGGGTC | 26094 |
rs766891640 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948390 | CCTAAATACATTAGC[A/G]ACCTGATTATAAATT | 26094 |
rs766892392 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940334 | AGAAGGAGATGGAGA[A/G]CAAGAGACTGCGGCT | 26094 |
rs766977736 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954135 | CCTAGAAGGCAGCCA[C/T]ACTTTACATTCTCCT | 26094 |
rs767090709 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938781 | CTATGTATGACACTC[C/T]TGTGAACAGAGCTTG | 26094 |
rs767097413 | in-del | -/G | 1.68495e-05 | 0.00290249 | frameshift-variant, intron-variant | DCAF4 | GRCh38.p7 | 14:72958732 | CTTCTCGTCGCGGCT[-/G]GGGGGGCTCCCGGGG | 26094 |
rs767119800 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941796 | CGAAAAAGCCAGCTG[A/G]GTTTTCTCAACGTCA | 26094 |
rs767278512 | snp | A/C | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925287 | TTTCCTTCCAAGACT[A/C]CCCTCCCATCCAGCC | 26094 |
rs767278628 | snp | C/G | 3.29462e-05 | 0.00405857 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954186 | CCGGCCTGGCATGCT[C/G]TGCAGTTTCCGGATC | 26094 |
rs767291849 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957611 | TGTTTTTATCACAGA[A/C]GAGCTCTTGTGAGCT | 26094 |
rs767369040 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934338 | TTTGTATTTTTAGTA[G/T]AGACGGGGTTTCTCC | 26094 |
rs767421940 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940844 | GATCTGCCTGCCTCA[A/G]CCTCCCAAAGTGCTG | 26094 |
rs767562032 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948255 | TGCAGTGGTACAATC[A/G]TAGCTCACTCCAGCC | 26094 |
rs767562256 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945955 | CAAGTATGGTATCAT[C/T]AACCTGCAAAGTCTG | 26094 |
rs767615309 | snp | C/T | 1.73156e-05 | 0.00294236 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938103 | GGGAGCCACTTTTGC[C/T]CAGTGTGCTTCTGGC | 26094 |
rs767645912 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935545 | CAGGCGTGAGCCACC[A/G]CATCCGGCCTTTAAA | 26094 |
rs767693888 | in-del | -/G | 1.6544e-05 | 0.00287606 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943106 | TACTGGTGAGTGGGA[-/G]GGGGGACACCTGCCT | 26094 |
rs767749459 | in-del | -/TATATAGTTT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953757 | ATATATATATATATA[-/TATATAGTTT]TATATAGTTTATTTA | 26094 |
rs767810954 | snp | A/C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942277 | TGAAATAGGCCGATA[A/C/G]TTTCCCCCATTTCCT | 26094 |
rs767832688 | snp | A/G | 8.32238e-05 | 0.00645019 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954505 | TGGATTGGGACAGGC[A/G]GAATATAAAAGTTTG | 26094 |
rs767849909 | snp | A/G | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72959688 | ATGACTTAGGAGATC[A/G]TGAGCTTGGGCTGCT | 26094 |
rs767886019 | snp | C/T | 1.66156e-05 | 0.00288228 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955543 | TCTGCTGTTTAATGG[C/T]TGCCGCTCTGGGGAA | 26094 |
rs767908958 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941500 | GTCCCCCCGGGTGTA[C/T]GTGGATGGGGAGCGT | 26094 |
rs767937789 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | DCAF4 | GRCh38.p7 | 14:72951814 | CTATGCCTCATGGGA[C/T]TCGCAGAGACTCCAG | 26094 |
rs767977697 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935357 | CCACCTGGGTTCAAA[C/T]GATTCTCCTGCCTCA | 26094 |
rs767982933 | snp | A/C | 3.69529e-05 | 0.00429826 | stop-gained, intron-variant | DCAF4 | GRCh38.p7 | 14:72958799 | TTACTGTTACTCCTA[A/C]AGCTAATTCTGCAGG | 26094 |
rs768105396 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931571 | TACAATGTTGAACAG[A/G]TGTATTGAGAACCAA | 26094 |
rs768111454 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940255 | GACCCTGAAAAGAAA[C/T]GCTACTTCCGCTTGC | 26094 |
rs768128777 | snp | A/G | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72962016 | GCATCTCTTCCCTTC[A/G]TAGCCCTCAACCTGA | 26094 |
rs768156098 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | DCAF4 | GRCh38.p7 | 14:72954262 | AACTGCTTCAGTACA[C/G]GTGAGCCTGGCTCCC | 26094 |
rs768194684 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947321 | GCACTTACATCTCAC[A/G]CTTTAGAAAAAAAAG | 26094 |
rs768326831 | snp | A/C | | | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940361 | GGCTGCTCCAGGAAG[A/C]AGACAGACGGAAAAA | 26094 |
rs768336225 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947043 | AGAGGAGCAGGACGT[C/G]AAGAGAGAAGTCACA | 26094 |
rs768344783 | snp | C/T | 1.69738e-05 | 0.00291317 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938081 | GACAGGCAAGTGTGC[C/T]GCTCTGGGGAGCCAC | 26094 |
rs768363946 | in-del | -/TGT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928522 | CTTACAAAATTCCCC[-/TGT]TGTTGGATATCTAGG | 26094 |
rs768377022 | snp | C/T | 1.68495e-05 | 0.00290249 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958732 | CCTTCTCGTCGCGGC[C/T]GGGGGGCTCCCGGGG | 26094 |
rs768426292 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928343 | AGACTACGGGCGCAC[A/G]CCACCGCGCCCGGCT | 26094 |
rs768454968 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925079 | ACCACGCCCGGCTAA[C/T]TTTTTGTATTTTTAG | 26094 |
rs768527425 | snp | A/G | 1.71917e-05 | 0.00293182 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955728 | TTTCTCAGGCCACAG[A/G]GTCTCGTGGCCCAGT | 26094 |
rs768667065 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925853 | ATGATAGATCCGATT[C/T]CTTCTCTCAACAGAA | 26094 |
rs768685218 | snp | C/T | 1.69815e-05 | 0.00291384 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940388 | AAAAGGTGGGCTCCT[C/T]ACCCCTTCGCCCCCT | 26094 |
rs768688564 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940870 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 26094 |
rs768708466 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946682 | GTCATCCAGCCAGGC[C/T]GCAGCCAGCACTGAG | 26094 |
rs768743315 | snp | C/T | 3.29859e-05 | 0.00406102 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958630 | GCCAGGACTGCTACA[C/T]GAGAATCTGGAGCCT | 26094 |
rs768760344 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955612 | GGGATGGAAGGCCAC[C/T]CGCCTGTTTCATGAT | 26094 |
rs768785159 | in-del | -/T | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935158 | CACACTCCCCACCCC[-/T]GAACAGGCTTCTTAA | 26094 |
rs768818535 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945689 | TTGTTAGATCAGACA[C/T]GTGCTGGCTTTGCCC | 26094 |
rs768848294 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936911 | ACCAAGAGAAAGATA[C/T]TACAGAAGCCAAAGG | 26094 |
rs768864757 | snp | A/G/T | 6.59059e-05 | 0.00574014 | missense | DCAF4 | GRCh38.p7 | 14:72951808 | TCCAGGCTATGCCTC[A/G/T]TGGGACTCGCAGAGA | 26094 |
rs768918283 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940302 | CTGCAACCCCCTGAC[A/G]AAAGAGAGCATCCGG | 26094 |
rs768920006 | snp | A/G | 0.000165525 | 0.00909587 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951922 | TGTCCTCTGTCTCCC[A/G]AGAGCTGTGTGGGGG | 26094 |
rs769023071 | snp | C/T | 1.8861e-05 | 0.00307085 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937935 | GCCCATGCCCACACA[C/T]AGAGATGTATGGATT | 26094 |
rs769122783 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936749 | TTGGTGCTCAGTAGC[A/G]ATATTAGGGTTGGAG | 26094 |
rs769157467 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942024 | CTCTAGAGCGAAGGC[A/G]GGGGACTCTTGCAGG | 26094 |
rs769251977 | snp | A/G | 1.65842e-05 | 0.00287955 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943118 | GGGAGGGGGACACCT[A/G]CCTAGGGTGTGGCTG | 26094 |
rs769255366 | snp | A/G | 1.68286e-05 | 0.0029007 | synonymous-codon, missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938065 | ACTCCGTGATTCTGA[A/G]GACAGGCAAGTGTGC | 26094 |
rs769325817 | snp | C/T | 3.31268e-05 | 0.00406968 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945835 | CCCTCTTAGGCAGTC[C/T]ACCAGGCGCAGCCTG | 26094 |
rs769417772 | snp | C/T | 0.000171154 | 0.00924919 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955501 | ATGATAGCCAGGCAC[C/T]GAGCAGTCCCTCTTT | 26094 |
rs769426320 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926739 | GGCGCGCTCCGCCCG[C/T]TCTGGGGCGCGTGGG | 26094 |
rs769474385 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | DCAF4 | GRCh38.p7 | 14:72955599 | GAAATCAAGGCAAGG[A/G]ATGGAAGGCCACCCG | 26094 |
rs769482493 | snp | C/G | 1.7649e-05 | 0.00297055 | splice-acceptor-variant, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72937970 | TGTTTTTCTCTTTTA[C/G]GAACAGAAATGAATA | 26094 |
rs769534777 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960465 | CGATTCTTAAATATA[C/T]TTAATCCGTCCGCCC | 26094 |
rs769535864 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945920 | CTCTTCACAGTGAAC[C/G]ATGTTAAAGTTGGAG | 26094 |
rs769678074 | snp | C/T | 3.30671e-05 | 0.00406602 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940365 | GCTCCAGGAAGAAGA[C/T]AGACGGAAAAAGGTG | 26094 |
rs769746157 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956533 | GGGAAGTTCCACCCC[A/G]TCAAATACTGTCTCT | 26094 |
rs769785709 | in-del | -/CT | 3.39957e-05 | 0.0041227 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956358 | CCCCCTGGCCCCTCC[-/CT]GATGGCCCCTGGTGC | 26094 |
rs769817970 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951788 | AACTGTCCTTAACAG[C/T]TTTTTCCAGGCTATG | 26094 |
rs769887751 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947551 | TGACGGGAGGCTCTG[A/G]GTTCACTACACAGAC | 26094 |
rs769905000 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932091 | CCTCCCAGGTTCAAG[A/C]GATTCTCCTGCCTCA | 26094 |
rs769917379 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945529 | CATTTTTCCTATTGC[A/G]CCACAGCCTTCGTGA | 26094 |
rs769974211 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924889 | TCACTTCCCAACTCT[A/G]GAACCCTCAGAGCCT | 26094 |
rs770022420 | in-del | -/AAAT | 1.65315e-05 | 0.00287498 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941700 | CCATCATCCCCTAAC[-/AAAT]AAATCTTCATTGAAT | 26094 |
rs770044367 | snp | A/G/T | 3.29458e-05 | 0.00405857 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947202 | ATTCTGTATCCTTTG[A/G/T]CAGAGGAAGAGGTTT | 26094 |
rs770132970 | in-del | -/ATATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[-/ATATATATATA]TATATATATATATAT | 26094 |
rs770246878 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943033 | CTGCATGGAGAGGAA[A/G]AAGGTCCAGATTCGA | 26094 |
rs770270937 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954766 | AAACCATTTTTAAAA[G/T]GTATAAGCCAAACAC | 26094 |
rs770298487 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952148 | TTCGGACGCCCGTGC[A/G]CATCATTCAGAAAAC | 26094 |
rs770340694 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933746 | TTGTTCAAAATCAGA[C/T]TTACTCTCCTCTCCC | 26094 |
rs770473607 | snp | A/G | 1.72169e-05 | 0.00293396 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942951 | GAATCTTCTTCATGG[A/G]TGTCAGCTTCAGCAT | 26094 |
rs770553929 | snp | G/T | 1.64838e-05 | 0.00287083 | missense | DCAF4 | GRCh38.p7 | 14:72954461 | CCAACAGTGATGTCT[G/T]GGCCCAGCAGTTTGC | 26094 |
rs770602780 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942927 | GGGCAGGGAAGGCCA[C/G]AGACCCCCGAATCTT | 26094 |
rs770606903 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943068 | TGGATCCCTCCGCCT[C/T]GGCAAGCGACCGATT | 26094 |
rs770608869 | snp | A/G | 5.15017e-05 | 0.00507427 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955495 | GATGTCATGATAGCC[A/G]GGCACTGAGCAGTCC | 26094 |
rs770806933 | snp | C/G | 8.23635e-05 | 0.00641677 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940295 | ATAACAACTGCAACC[C/G]CCTGACGAAAGAGAG | 26094 |
rs770856912 | snp | G/T | 1.65553e-05 | 0.00287705 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946062 | AGCCTCTCTGCACAC[G/T]TGACCCTGGGGGTAG | 26094 |
rs770906297 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949243 | TGCTTGAGGCCAGGA[A/G]TTTGAGACCAGCCTG | 26094 |
rs770978025 | snp | A/G | 1.80205e-05 | 0.00300165 | missense | DCAF4 | GRCh38.p7 | 14:72956422 | ACCACGAAGTGCGTA[A/G]GGCAGTACGAAGGCC | 26094 |
rs771022758 | in-del | -/TAAA | | | utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961393 | ACTTTTCTAACAGGG[-/TAAA]TAAACCCTCCTCCCA | 26094 |
rs771060607 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938245 | CCTAACGTGCTCCCA[C/G]GGCATGTCGCTTTGG | 26094 |
rs771083635 | snp | A/T | 3.43731e-05 | 0.00414552 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956355 | GTACCCCCTGGCCCC[A/T]CCCTGATGGCCCCTG | 26094 |
rs771103731 | in-del | -/A | 1.7117e-05 | 0.00292544 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942961 | ATGGATGTCAGCTTC[-/A]AGCATCCATGCCCCC | 26094 |
rs771166928 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924752 | CCCTGGTTTGGCCCT[C/T]ACTACCTTTCACAAG | 26094 |
rs771231029 | snp | A/G | | | missense | DCAF4 | GRCh38.p7 | 14:72954181 | ATAGACCGGCCTGGC[A/G]TGCTCTGCAGTTTCC | 26094 |
rs771293064 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957040 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATAC | 26094 |
rs771297091 | in-del | -/GCCGTATCCTGGGGCTCTTCCCGGCA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942603 | GCGAAACAAGAGGCG[-/GCCGTATCCTGGGGCTCTTCCCGGCA]GCCGTATCCTGGGGC | 26094 |
rs771299818 | in-del | -/CCATT | 1.65172e-05 | 0.00287373 | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72955555 | GGCTGCCGCTCTGGG[-/CCATT]GAAATCTTTGCCATT | 26094 |
rs771377842 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933186 | AAATGTCTCCAGACA[C/T]TGCCAGATGTCCCCT | 26094 |
rs771428189 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941856 | TTGTTATGTTTTCTT[C/T]ATGAATGTTCTTTTC | 26094 |
rs771465868 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942383 | CACCTGAGCGCCCAG[C/T]GCTGCGTCTCCTGCC | 26094 |
rs771491477 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957879 | GTGTGTCACAGTCCT[C/T]AGAACTGGAGCCCTG | 26094 |
rs771526627 | snp | G/T | 1.64841e-05 | 0.00287085 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954444 | CCGGCAGTCCTTTGG[G/T]ACCAACAGTGATGTC | 26094 |
rs771551490 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944959 | CTGGGTGTGGTGGTG[C/T]GCACCTGTAGTCCCA | 26094 |
rs771560966 | snp | C/T | 0.000100523 | 0.00708881 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958726 | GTGTGGCCTTCTCGT[C/T]GCGGCTGGGGGGCTC | 26094 |
rs771758520 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940923 | CATTTTGTCATTCCT[A/G]AAGGAATCTTGGGAG | 26094 |
rs771815757 | in-del | -/TTCT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930865 | CAGTTGAAAAGACAC[-/TTCT]TTCTTTCATTGAATG | 26094 |
rs771941250 | snp | C/T | 4.94181e-05 | 0.00497057 | missense | DCAF4 | GRCh38.p7 | 14:72947149 | CTCACCAGGTGAATT[C/T]GGTGTGCTGGGCCTC | 26094 |
rs771974972 | snp | A/T | 1.64751e-05 | 0.00287007 | missense | DCAF4 | GRCh38.p7 | 14:72955621 | GGCCACCCGCCTGTT[A/T]CATGATTCAGCAGTG | 26094 |
rs771994118 | snp | A/T | 3.37285e-05 | 0.00410647 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939913 | GCCAGGTAAGGCCAC[A/T]TGCGGGGTGGGAATC | 26094 |
rs772009343 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946903 | GTAGAAAATTCAGCC[C/G]TGCCCAGAGGGTATG | 26094 |
rs772017876 | in-del | -/C | 1.65029e-05 | 0.00287248 | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72955561 | CCGCTCTGGGGAAAT[-/C]TTTGCCATTGATCTG | 26094 |
rs772059357 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960240 | CCGCACCCTCCACCT[A/C]CTGGGTTCTAGTGAT | 26094 |
rs772205344 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948019 | GTGACTACTCATTGT[A/T]CCTCACACCTACTTC | 26094 |
rs772228393 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941729 | TGAATTGTTCTCTTT[C/T]TTGTAATAAATATAG | 26094 |
rs772258272 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937110 | TCGTAGATGTAGACC[A/G]TTCTTTCAGAATATG | 26094 |
rs772311591 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950183 | TTCCTTTGGTGGCAT[C/T]GTTGGGGGATAGACG | 26094 |
rs772330861 | snp | C/T | 1.75511e-05 | 0.0029623 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940407 | CCTTCGCCCCCTGTC[C/T]TCTCCGCTCCTGCCA | 26094 |
rs772428988 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955401 | AAACCCTGACCAGCA[C/T]GTGTCTAATCACACC | 26094 |
rs772460878 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944200 | TTACGTGTGGTAGGT[C/T]GTCTCCATCACCCAA | 26094 |
rs772570032 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929938 | AGAGCCATGGCTGCT[A/G]CTCTCCATGGCGGCC | 26094 |
rs772577829 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943158 | GGACACTTTGTGGCT[C/T]AGCGTTGCCAGTCAT | 26094 |
rs772679642 | snp | A/G | 1.6743e-05 | 0.0028933 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956550 | CAAATACTGTCTCTC[A/G]GGGGCGATCCCAGCA | 26094 |
rs772685054 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941078 | AAGTGATCCTCCTGC[C/T]TCAGCCTCCCAAGTA | 26094 |
rs772755637 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951021 | GGTCTTACTCTGTCA[C/T]CCAGGCTGGAGTGCG | 26094 |
rs772756697 | snp | C/T | 1.69991e-05 | 0.00291535 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942967 | TGTCAGCTTCAGCAT[C/T]CATGCCCCCACCCTC | 26094 |
rs772815628 | snp | C/T | 1.65485e-05 | 0.00287645 | missense | DCAF4 | GRCh38.p7 | 14:72954394 | CCGCCAGGCTTGTCT[C/T]GGCGGGTCCTGTTGA | 26094 |
rs772825005 | in-del | -/GA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72942591 | TGTTCCTCACCCTGC[-/GA]AACAAGAGGCGGCCG | 26094 |
rs772833445 | snp | G/T | 3.29598e-05 | 0.00405941 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943055 | CAGATTCGAAGCATG[G/T]ATCCCTCCGCCTTGG | 26094 |
rs772852176 | snp | A/G | 3.29641e-05 | 0.00405968 | missense | DCAF4 | GRCh38.p7 | 14:72954448 | CAGTCCTTTGGGACC[A/G]ACAGTGATGTCTTGG | 26094 |
rs772975815 | snp | A/G | 1.7159e-05 | 0.00292903 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958745 | GCTGGGGGGCTCCCG[A/G]GGCGCGCCGGGGCTG | 26094 |
rs773027183 | snp | A/G | 1.87282e-05 | 0.00306002 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958835 | GCCCAGAGCCATGTG[A/G]ATTTGACTTACGGGA | 26094 |
rs773081041 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960257 | TGGGTTCTAGTGATT[C/G]TCCTGCCTCAGCCTC | 26094 |
rs773193083 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927666 | TGAGGTGGTGTTCTG[C/T]GGGTAACCAGGCCTG | 26094 |
rs773208130 | snp | A/C | 1.75302e-05 | 0.00296054 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955745 | TCTCGTGGCCCAGTG[A/C]CCTGCCAGGTGAAAG | 26094 |
rs773225549 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950198 | TGTTGGGGGATAGAC[A/G]GACGAGAGCAAGTCC | 26094 |
rs773240052 | snp | C/T | 1.65176e-05 | 0.00287376 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946050 | GCCCATCCCTGTAGC[C/T]TCTCTGCACACTTGA | 26094 |
rs773293605 | in-del | -/T | 1.64757e-05 | 0.00287012 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956369 | CTCCCTGATGGCCCC[-/T]GGTGCTTTTTCCACA | 26094 |
rs773299046 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937322 | TACCTGTTGTCCAAG[A/G]CAAGGAAGAAGACAA | 26094 |
rs773420085 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72952061 | CTTTTTACCCATCTT[G/T]GGCCATTTCAGTCAT | 26094 |
rs773471575 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945968 | ATCAACCTGCAAAGT[C/T]TGAAGACCCCTACGC | 26094 |
rs773476355 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943227 | GGTGGCATCTTCTTG[G/T]TTGTACGATTTTAAC | 26094 |
rs773502810 | snp | C/T | 0.0001755 | 0.00936586 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940409 | TTCGCCCCCTGTCCT[C/T]TCCGCTCCTGCCAGC | 26094 |
rs773592960 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954116 | CCCAGTGGTCCCTGG[C/T]CTGCCTAGAAGGCAG | 26094 |
rs773614242 | in-del | -/CTC | 1.65018e-05 | 0.00287239 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941723 | CTTCATTGAATTGTT[-/CTC]TTTTTTGTAATAAAT | 26094 |
rs773688467 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955802 | AAGACCCCAGGCAGG[C/G]GAATTTCGCTGAAGA | 26094 |
rs773709696 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72944327 | ATTCTTCTGGGAACA[C/T]AACTTCTTCCTGAGT | 26094 |
rs773715840 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72951816 | ATGCCTCATGGGACT[C/T]GCAGAGACTCCAGGC | 26094 |
rs773833882 | snp | G/T | 1.68684e-05 | 0.00290412 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958733 | CTTCTCGTCGCGGCT[G/T]GGGGGCTCCCGGGGC | 26094 |
rs773905740 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931673 | GTATTTTGTAGATGC[A/T]CCTTATCAGGTTGAG | 26094 |
rs773912216 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949862 | TGTGTGGTCATTCAG[A/C]CAACACCTATCGAGT | 26094 |
rs773971590 | snp | A/G/T | 8.24048e-05 | 0.00641844 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954381 | CCCATCTCTGTCTCC[A/G/T]CCAGGCTTGTCTCGG | 26094 |
rs773976875 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72926994 | TGTGCTGCCGGCTTC[A/T]CAGGCGCTAACATTT | 26094 |
rs774004179 | snp | A/C | 1.85775e-05 | 0.00304769 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958808 | CTCCTACAGCTAATT[A/C]TGCAGGGCACAGCCC | 26094 |
rs774062076 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941784 | TCTTCCATGCTACGA[A/G]AAAGCCAGCTGGGTT | 26094 |
rs774117802 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945847 | GTCCACCAGGCGCAG[C/T]CTGGGACGTCACCCA | 26094 |
rs774251696 | snp | C/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924980 | GCAATGGCGCTATCT[C/T]GGCTCACTGCAACCC | 26094 |
rs774272480 | snp | A/G | 3.40032e-05 | 0.00412316 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938082 | ACAGGCAAGTGTGCC[A/G]CTCTGGGGAGCCACT | 26094 |
rs774305777 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940880 | ACAGGCGTGAGCCAC[C/T]ACACCCAGCCTTCTT | 26094 |
rs774307526 | snp | G/T | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925194 | GCTGGGATTTCAGGC[G/T]TGAGCCACTGCACCC | 26094 |
rs774335223 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958422 | CACAGCCAACCAGGG[A/C]ATCTTGTCATTGTTC | 26094 |
rs774360908 | snp | A/C | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72926054 | TCGCCGCCAGTCGTA[A/C]CATCACGTTACTTCT | 26094 |
rs774379172 | snp | C/T | 4.94246e-05 | 0.0049709 | missense | DCAF4 | GRCh38.p7 | 14:72955613 | GGATGGAAGGCCACC[C/T]GCCTGTTTCATGATT | 26094 |
rs774441580 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946690 | GCCAGGCCGCAGCCA[A/G]CACTGAGGCTTAAAC | 26094 |
rs774528760 | snp | G/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940308 | CCCCCTGACGAAAGA[G/T]AGCATCCGGCAGAAG | 26094 |
rs774561690 | in-del | -/T | 1.65038e-05 | 0.00287257 | frameshift-variant, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943088 | GCGACCGATTTAACC[-/T]TCATACTGGTGAGTG | 26094 |
rs774567508 | snp | C/T | 1.72282e-05 | 0.00293492 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940400 | CCTCACCCCTTCGCC[C/T]CCTGTCCTCTCCGCT | 26094 |
rs774580875 | snp | A/G | | | missense | DCAF4 | GRCh38.p7 | 14:72954241 | TCCCTGAATATCCAA[A/G]CAAATAACTGCTTCA | 26094 |
rs774605075 | snp | C/G | 4.96693e-05 | 0.00498319 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951926 | CTCTGTCTCCCGAGA[C/G]CTGTGTGGGGGTGGC | 26094 |
rs774623930 | in-del | -/AAAT | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945402 | CCACCTCTTAAAAAA[-/AAAT]AGCCTACATTTGAAT | 26094 |
rs774624332 | snp | C/T | 1.66333e-05 | 0.00288381 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72955540 | TCCTCTGCTGTTTAA[C/T]GGCTGCCGCTCTGGG | 26094 |
rs774624409 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934184 | TTGAGACGGAGTCTC[A/G]CTCTGTTGCTCAAGG | 26094 |
rs774730184 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956522 | GAGGAAGGAAGGGGA[A/G]GTTCCACCCCATCAA | 26094 |
rs774806404 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956990 | GGCCAAGGAGGGTGG[A/G]TCACGAGGTCAGGAG | 26094 |
rs774892180 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72955148 | CATTACTATATTTCA[C/T]AGACTTTTCTCTAGA | 26094 |
rs774977386 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945923 | TTCACAGTGAACGAT[G/T]TTAAAGTTGGAGGCT | 26094 |
rs775000373 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72935215 | CCTAGCCTTTAAACT[C/T]TTACTGTATTTGGAA | 26094 |
rs775001157 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929749 | CCTTGAAGACCTTCA[C/G]TGACTCCATGGCGCG | 26094 |
rs775146316 | snp | A/G | 1.68935e-05 | 0.00290628 | intron-variant | DCAF4 | GRCh38.p7 | 14:72938075 | TCTGAAGACAGGCAA[A/G]TGTGCCGCTCTGGGG | 26094 |
rs775147573 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960552 | TGCACTGTGCCCCCT[C/G]AGCATTGTGGCTGAC | 26094 |
rs775181432 | in-del | -/TATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928588 | AGTAAACATCCTTTA[-/TATATATATA]TATATATATATATAT | 26094 |
rs775188612 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954156 | ACATTCTCCTATCCC[C/T]TTAGCAGGAATAGAC | 26094 |
rs775241247 | snp | C/T | 8.25076e-05 | 0.00642238 | intron-variant, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954480 | CCAGCAGTTTGCTCT[C/T]ATGGTTGGTTGGATT | 26094 |
rs775344493 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948443 | GTGTTCTCTAAATTG[C/T]AAATTTTATGTGGCT | 26094 |
rs775413346 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957160 | GAGGTTGCAGTGAGC[C/T]GATATCACGCCACTG | 26094 |
rs775414910 | snp | A/G | 1.65534e-05 | 0.00287688 | intron-variant | DCAF4 | GRCh38.p7 | 14:72945836 | CCTCTTAGGCAGTCC[A/G]CCAGGCGCAGCCTGG | 26094 |
rs775427743 | snp | A/C | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72924900 | CTCTAGAACCCTCAG[A/C]GCCTCCCATTGTCTA | 26094 |
rs775480672 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932146 | GGTGTGCACCACCAC[A/G]CCTAACTAATTTTTT | 26094 |
rs775597108 | snp | A/G | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935069 | TATGAACAAACAGTC[A/G]TGCAGAGTGATGAGT | 26094 |
rs775674583 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958278 | ACCCTGTCCCTAAAA[A/C]ATGGGGGAAATCAGT | 26094 |
rs775690983 | in-del | -/AT | 1.66905e-05 | 0.00288876 | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72955685 | CTGATGGCTTCAGAC[-/AT]GGCTGGAAAGGTAGG | 26094 |
rs775704486 | snp | G/T | 1.6477e-05 | 0.00287024 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951793 | TCCTTAACAGCTTTT[G/T]CCAGGCTATGCCTCA | 26094 |
rs775707723 | in-del | -/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954296 | TGCCCAGAGAAGAGG[-/C]CCTTAACAGGCCTTA | 26094 |
rs775796928 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940178 | CTCAGGTGGTCAGTT[C/T]ACAGTGGTTGAAATT | 26094 |
rs775819176 | snp | A/C | 2.45396e-05 | 0.00350274 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956380 | CCCCTGGTGCTTTTT[A/C]CACAGATCAAGCTGT | 26094 |
rs775994473 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933840 | TTTCTCAACTCCTCT[A/C]TCCACCTCTCCCATG | 26094 |
rs776113076 | snp | A/G | 1.72151e-05 | 0.00293381 | intron-variant | DCAF4 | GRCh38.p7 | 14:72942953 | ATCTTCTTCATGGAT[A/G]TCAGCTTCAGCATCC | 26094 |
rs776187879 | snp | G/T | 1.78426e-05 | 0.00298681 | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72937966 | TTTTTGTTTTTCTCT[G/T]TTAGGAACAGAAATG | 26094 |
rs776224987 | snp | A/G | 3.29647e-05 | 0.00405971 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943069 | GGATCCCTCCGCCTT[A/G]GCAAGCGACCGATTT | 26094 |
rs776278286 | snp | A/C/G | 3.34321e-05 | 0.00408842 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943139 | GGTGTGGCTGCCACC[A/C/G]TCTGGACACTTTGTG | 26094 |
rs776334041 | snp | C/T | 1.67835e-05 | 0.0028968 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956555 | ACTGTCTCTCAGGGG[C/T]GATCCCAGCAACTTC | 26094 |
rs776367639 | snp | A/G | 1.87848e-05 | 0.00306465 | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958848 | TGGATTTGACTTACG[A/G]GAGTAAAGCGTAACT | 26094 |
rs776379484 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949370 | CTGAGGCAGGAGGAT[A/C]ATTTGAGCCCCAGAG | 26094 |
rs776400170 | snp | A/G | 7.19088e-05 | 0.00599577 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939917 | GGTAAGGCCACTTGC[A/G]GGGTGGGAATCCTGG | 26094 |
rs776432804 | in-del | -/GGGACACCTGCCTAGGGTGT | 1.65523e-05 | 0.00287678 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943108 | CTGGTGAGTGGGAGG[-/GGGACACCTGCCTAGGGTGT]GGGACACCTGCCTAG | 26094 |
rs776494041 | snp | C/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72959416 | AGATGGATCTTCTTA[C/T]ATGCTAGAAGTTTTA | 26094 |
rs776522600 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72948272 | AGCTCACTCCAGCCT[A/G]GAACTCCTGGGCTCA | 26094 |
rs776535294 | snp | C/G | 1.6486e-05 | 0.00287102 | intron-variant, synonymous-codon | DCAF4 | GRCh38.p7 | 14:72954465 | CAGTGATGTCTTGGC[C/G]CAGCAGTTTGCTCTC | 26094 |
rs776547723 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960399 | AGGTGATCTGCCCGC[C/T]TCAGCCTCCCAAAGT | 26094 |
rs776578024 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937694 | AAAGTGCTGGGATTA[C/G]AGGCATGAGCCACCG | 26094 |
rs776795736 | snp | C/G | 3.29788e-05 | 0.00406058 | intron-variant | DCAF4 | GRCh38.p7 | 14:72956360 | CCCTGGCCCCTCCCT[C/G]ATGGCCCCTGGTGCT | 26094 |
rs776829754 | snp | C/T | 2.03556e-05 | 0.0031902 | synonymous-codon, missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939844 | TCACGATTCCGGCCA[C/T]GGTGATGACGAGTCT | 26094 |
rs776853264 | snp | A/C | 8.94975e-05 | 0.00668885 | missense | DCAF4 | GRCh38.p7 | 14:72956426 | CGAAGTGCGTAAGGC[A/C]GTACGAAGGCCACGT | 26094 |
rs776914373 | snp | C/T | 6.68684e-05 | 0.00578184 | intron-variant | DCAF4 | GRCh38.p7 | 14:72946068 | TCTGCACACTTGACC[C/T]TGGGGGTAGTTGGCC | 26094 |
rs777160875 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931773 | TGCTTTTTCTGTGTA[C/T]CAATTGAGAAAATCA | 26094 |
rs777205793 | snp | A/G | 1.64893e-05 | 0.0028713 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941861 | ATGTTTTCTTCATGA[A/G]TGTTCTTTTCCTGTT | 26094 |
rs777289797 | snp | C/T | 3.29484e-05 | 0.00405871 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941767 | GGATGGGATTTAATG[C/T]ATCTTCCATGCTACG | 26094 |
rs777319455 | snp | A/G | 3.44495e-05 | 0.00415013 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955483 | CAGCCTCAGAGGGAT[A/G]TCATGATAGCCAGGC | 26094 |
rs777408904 | snp | C/T | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935104 | ACATGGACTATAAAG[C/T]GGCCATAGAGAATGA | 26094 |
rs777411102 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947313 | ACCCTTGTGCACTTA[C/T]ATCTCACGCTTTAGA | 26094 |
rs777487700 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72947046 | GGAGCAGGACGTGAA[A/G]AGAGAAGTCACACGT | 26094 |
rs777508884 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931035 | TGAATTTTGAAATTG[C/T]GAGGTGCGAGTCATC | 26094 |
rs777533823 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929557 | TATTTTTTATTTTTA[C/T]TTTATTTTTCCGTCA | 26094 |
rs777545165 | snp | A/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940278 | CCGCTTGCTCCCTGG[A/T]CATAACAACTGCAAC | 26094 |
rs777594951 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953395 | CAATCTGTACGTTCT[A/G]TCAATGCAAAAGTTT | 26094 |
rs777624276 | snp | A/G | | | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941795 | ACGAAAAAGCCAGCT[A/G]GGTTTTCTCAACGTC | 26094 |
rs777705217 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934106 | TTCAGGCTCTGGCCA[C/T]ACCAAACAGCCTGCA | 26094 |
rs777720362 | snp | C/T | 1.8251e-05 | 0.00302079 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72956418 | GAGGACCACGAAGTG[C/T]GTAAGGCAGTACGAA | 26094 |
rs777776135 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951748 | TAAATGTCCATGCCT[C/T]CTCCCAGAGGGGAGC | 26094 |
rs777781868 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930964 | TGCTACTCCATTGAT[A/C]TATATTTCTATCCAT | 26094 |
rs777854367 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949189 | CATGGTGGCTCCCAC[C/T]GGTAATCTCAGCATT | 26094 |
rs777879281 | snp | G/T | 1.64827e-05 | 0.00287073 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941843 | AGACAATGCCTCTTT[G/T]TTATGTTTTCTTCAT | 26094 |
rs777907961 | snp | C/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938162 | CAGGTGTGGAGATCA[C/G]CTGGGGGCTCGTCCC | 26094 |
rs778100857 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939243 | CCTTTACTACATCCT[G/T]CAGCCTATAATTCCC | 26094 |
rs778108554 | snp | A/T | 4.94548e-05 | 0.00497242 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954343 | TCCCTCTCCCCAGAC[A/T]ACATGTGACATAATC | 26094 |
rs778152143 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72939250 | TACATCCTTCAGCCT[A/G]TAATTCCCTCAGAAG | 26094 |
rs778231631 | snp | C/T | 3.29636e-05 | 0.00405964 | synonymous-codon | DCAF4 | GRCh38.p7 | 14:72946012 | GCACGAAAACCTCTA[C/T]TTCACCAACCGGAAG | 26094 |
rs778257059 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | DCAF4 | GRCh38.p7 | 14:72954227 | GGTCCTGTGCCTGGT[C/G]CCTGAATATCCAAGC | 26094 |
rs778282462 | in-del | -/T | 5.13914e-05 | 0.00506883 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955500 | ATGATAGCCAGGCAC[-/T]TGAGCAGTCCCTCTT | 26094 |
rs778284999 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72945440 | TCTTTTTCTATTGCA[C/T]GTTTTATTCAATGCA | 26094 |
rs778312945 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956954 | GCGGTGGCTCACGCC[C/T]GTAATCCCAACACTT | 26094 |
rs778338547 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72933044 | GCACCCAGCCCTGGA[C/T]AATTCTTGCTGAAGA | 26094 |
rs778351509 | snp | A/G | 1.80309e-05 | 0.00300252 | synonymous-codon, intron-variant | DCAF4 | GRCh38.p7 | 14:72958775 | GCTCATGGCTGTCGG[A/G]CAGGACCTTTACTGT | 26094 |
rs778367986 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957721 | TCAGCTTCAGCCAAG[A/G]TAGCACTTCTGGTCT | 26094 |
rs778535290 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946105 | AGGGTAGAGGAGAGC[A/G]ACTGGGGAAGAGGGC | 26094 |
rs778590362 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72934618 | CATTCTTCAGACTGC[A/C]CTTATCTCCCTCCCC | 26094 |
rs778729072 | snp | C/T | | | | | GRCh38.p7 | 14:72951685 | GTTGAATCTGGACGG[C/T]GGGGGTTACTCTGGC | 26094 |
rs778737546 | snp | C/T | | | | | GRCh38.p7 | 14:72951988 | ACTGTGGGAGGATTC[C/T]CTAAGCCTGTCCCAG | 26094 |
rs778771457 | in-del | -/AAAAAAA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953710 | ACAAGACCCTGTCTT[-/AAAAAAA]AAAAAAAAAAAAAAA | 26094 |
rs778797519 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72941810 | GGGTTTTCTCAACGT[C/T]ACCAATTACTGCCAG | 26094 |
rs778924173 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72941642 | TTTCTGCCAATTTAG[C/T]GCCTGTTTCCTTCAT | 26094 |
rs778957873 | snp | A/G | 1.65795e-05 | 0.00287914 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958713 | GCCGACATTCCCAGT[A/G]TGGCCTTCTCGTCGC | 26094 |
rs778988482 | snp | C/G | 0.000391071 | 0.0139779 | intron-variant | DCAF4 | GRCh38.p7 | 14:72939759 | TCAGAATGGCTGGAA[C/G]TCAAGTCCTGGGCTG | 26094 |
rs778994046 | snp | A/C | | | downstream-variant-500B, intron-variant | DCAF4 | GRCh38.p7 | 14:72960009 | GCCGGGTTCCAGCAA[A/C]TCTTCATTTGTCCCT | 26094 |
rs778995330 | snp | A/G | 1.7203e-05 | 0.00293278 | intron-variant | DCAF4 | GRCh38.p7 | 14:72955729 | TTCTCAGGCCACAGG[A/G]TCTCGTGGCCCAGTG | 26094 |
rs779012938 | snp | G/T | 4.94181e-05 | 0.00497057 | missense | DCAF4 | GRCh38.p7 | 14:72954208 | TTCCGGATCCCTGGT[G/T]CCTGGTCCTGTGCCT | 26094 |
rs779028783 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941720 | AATCTTCATTGAATT[A/G]TTCTCTTTTTTGTAA | 26094 |
rs779094234 | in-del | -/TCTTTGC | 1.65125e-05 | 0.00287333 | frameshift-variant | DCAF4 | GRCh38.p7 | 14:72955557 | CTGCCGCTCTGGGGA[-/TCTTTGC]AATCTTTGCCATTGA | 26094 |
rs779113419 | snp | C/G | 1.64814e-05 | 0.00287061 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954308 | GAGGCCTTAACAGGC[C/G]TTAAAACCCCATGTA | 26094 |
rs779177564 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929473 | GCGCCAAGGCAGGAG[A/G]ATCGCTGGAGGCCAG | 26094 |
rs779189620 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937075 | GGGTTGAGGAATATC[A/G]GGAGATGAAGACATT | 26094 |
rs779252697 | snp | C/T | 3.31829e-05 | 0.00407313 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943119 | GGAGGGGGACACCTG[C/T]CTAGGGTGTGGCTGC | 26094 |
rs779309732 | snp | C/G | 1.87866e-05 | 0.00306479 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937939 | ATGCCCACACACAGA[C/G]ATGTATGGATTTTTT | 26094 |
rs779367097 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | DCAF4 | GRCh38.p7 | 14:72947125 | ACTTTCCATCTCGCT[A/G]TGTGCTTCCTCACCA | 26094 |
rs779372720 | snp | G/T | 1.64857e-05 | 0.00287099 | missense | DCAF4 | GRCh38.p7 | 14:72955570 | GGAAATCTTTGCCAT[G/T]GATCTGCGTTGTGGA | 26094 |
rs779472370 | snp | A/C/T | 6.04045e-05 | 0.00549538 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72939831 | CAGCACAGCCCGCTC[A/C/T]CGATTCCGGCCACGG | 26094 |
rs779484225 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951191 | TTGCTGTGTTTCCCA[G/T]GCTGGTCTCGAACTC | 26094 |
rs779495803 | snp | C/G | 3.29625e-05 | 0.00405958 | missense, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72945891 | TTCTCCAGGCAGATA[C/G]CAACAGTGACCGGCT | 26094 |
rs779510410 | in-del | -/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927371 | TTTTTTTTTTTTTTT[-/G]GAGGCGGAGTCTCGC | 26094 |
rs779636896 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72957653 | AGAGCTCAGCCTTGC[C/T]GAGAGGCAGATGCAG | 26094 |
rs779679797 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928227 | ATACGGAATTTCACT[A/G]TTGTTGCCCAGGCTG | 26094 |
rs779778858 | snp | A/G | 3.29516e-05 | 0.00405891 | missense | DCAF4 | GRCh38.p7 | 14:72955604 | CAAGGCAAGGGATGG[A/G]AGGCCACCCGCCTGT | 26094 |
rs779807802 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932928 | TTGTTTGTTTGAGAC[A/G]GGATCTTGCTATGTT | 26094 |
rs779881989 | in-del | -/T | 1.64795e-05 | 0.00287045 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940204 | AATTGGTGCATTTAA[-/T]TTTTTTTGTCTAAAG | 26094 |
rs779962191 | snp | A/C | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72938205 | GATTCTGTAGGTCTG[A/C]GGGGTCTTGAGGAGA | 26094 |
rs780000310 | snp | A/G | 4.95667e-05 | 0.00497804 | intron-variant | DCAF4 | GRCh38.p7 | 14:72941697 | TCTCCATCATCCCCT[A/G]ACAAATAAATCTTCA | 26094 |
rs780023131 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950597 | AAAAGGAGAGGAACC[A/G]CGTCAGTCAAAAGAC | 26094 |
rs780042252 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72949433 | TGCACTCCAGCCTGG[A/G]TGAAAGAGAGAGACC | 26094 |
rs780078625 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72951634 | AACAAACAAAAAAAA[A/G]ACATCTGAAGGTAAA | 26094 |
rs780084635 | snp | G/T | | | utr-variant-3-prime, intron-variant | DCAF4 | GRCh38.p7 | 14:72958880 | TTTACTGCATCTAAT[G/T]AGGGTGTTTTAAGTG | 26094 |
rs780141676 | snp | A/G | 0.000115463 | 0.00759725 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958618 | CTTTCCTAGTGGGCC[A/G]GGACTGCTACACGAG | 26094 |
rs780153726 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936846 | GGAAAGCACATACAG[A/G]GTGTGTGACCCAGGA | 26094 |
rs780235007 | snp | A/T | 1.65187e-05 | 0.00287386 | stop-gained, intron-variant | DCAF4 | GRCh38.p7 | 14:72958695 | CCGTACCCTGCCTCC[A/T]AGGCCGACATTCCCA | 26094 |
rs780275291 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940510 | GGGTGTGGCCCTAGC[A/T]TTTCCCTGACAGGAA | 26094 |
rs780279826 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946589 | GGGCCCACACCAGGG[C/T]ACAGAGTTCCTTGGA | 26094 |
rs780326421 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956541 | CCACCCCATCAAATA[C/T]TGTCTCTCAGGGGCG | 26094 |
rs780364542 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946429 | GATTTATGGTTGCTG[A/G]GAACCCATAGGGAAA | 26094 |
rs780402694 | snp | A/C/T | 3.31517e-05 | 0.00407123 | intron-variant | DCAF4 | GRCh38.p7 | 14:72943115 | AGTGGGAGGGGGACA[A/C/T]CTGCCTAGGGTGTGG | 26094 |
rs780412154 | snp | C/T | 7.60601e-05 | 0.00616638 | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937928 | CAGAAAAGCCCATGC[C/T]CACACACAGAGATGT | 26094 |
rs780451561 | snp | A/G | 0.000148308 | 0.00861 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943036 | CATGGAGAGGAAAAA[A/G]GTCCAGATTCGAAGC | 26094 |
rs780452931 | snp | C/T | 1.67388e-05 | 0.00289294 | synonymous-codon, missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938038 | AAGCCACCAGCAGAA[C/T]CCTTGGTTCAGACTC | 26094 |
rs780625072 | snp | G/T | 0.000134712 | 0.00820596 | splice-donor-variant | DCAF4 | GRCh38.p7 | 14:72955698 | ACATGGCTGGAAAGG[G/T]AGGGGATCATGGACT | 26094 |
rs780637756 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954520 | AGAATATAAAAGTTT[A/G]CCCCATGTAGAAATT | 26094 |
rs780761217 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956869 | CCTGTTGTCTCTACT[C/T]ACATTTCCACCAGAG | 26094 |
rs780793479 | in-del | -/CTC | 8.25621e-05 | 0.0064245 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951888 | CCCAGGTACAGGGTT[-/CTC]CTCCTTTAAAGAAAT | 26094 |
rs780835122 | snp | A/G | 0.000100595 | 0.00709137 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72938055 | CTTGGTTCAGACTCC[A/G]TGATTCTGAAGACAG | 26094 |
rs780897148 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72931165 | GAATTTTGATAGGGA[C/T]TGCATTCAATCTGTA | 26094 |
rs780903398 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | DCAF4 | GRCh38.p7 | 14:72955584 | TTGATCTGCGTTGTG[A/G]AAATCAAGGCAAGGG | 26094 |
rs781015263 | snp | A/G | 1.65061e-05 | 0.00287277 | splice-donor-variant | DCAF4 | GRCh38.p7 | 14:72951878 | TCAATAGTCACCCAG[A/G]TACAGGGTTCTCCTC | 26094 |
rs781028295 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72929673 | CTCAGCTCCTCCCGC[A/T]TCCTCTTGGCACGGA | 26094 |
rs781144681 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932862 | GTGTGAGCCATCACA[C/T]CCAGCTGAATAATTT | 26094 |
rs781154825 | snp | A/C | 1.64803e-05 | 0.00287052 | intron-variant | DCAF4 | GRCh38.p7 | 14:72951761 | CTCCTCCCAGAGGGG[A/C]GCCTTGTGCCTAACT | 26094 |
rs781212988 | snp | C/G | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72940296 | TAACAACTGCAACCC[C/G]CTGACGAAAGAGAGC | 26094 |
rs781243386 | in-del | -/AGA | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72937199 | AAAGCTGAGATAAGG[-/AGA]AGAAGGAGACATTAA | 26094 |
rs781246222 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936563 | GCGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 26094 |
rs781277870 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72956036 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 26094 |
rs781316555 | snp | C/G | 4.28128e-05 | 0.00462651 | missense | DCAF4 | GRCh38.p7 | 14:72956486 | TGCACGAGGAAGAAG[C/G]AATCCTGGTGGCAGG | 26094 |
rs781332188 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950519 | CCTGGATTTCAGTGG[A/G]GGAAAGGCAAGGGAA | 26094 |
rs781382175 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72958097 | CAGCTGGGGCAACAC[A/G]GCAAGACCCTATCTC | 26094 |
rs781406512 | snp | A/C | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925532 | GAGCTGAAATGCCTT[A/C]GCACGGCGTGCAATG | 26094 |
rs781501175 | snp | A/G | 1.83159e-05 | 0.00302615 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958789 | GGCAGGACCTTTACT[A/G]TTACTCCTACAGCTA | 26094 |
rs781533598 | in-del | -/C | 1.71857e-05 | 0.0029313 | intron-variant | DCAF4 | GRCh38.p7 | 14:72940398 | CTCCTCACCCCTTCG[-/C]CCCCTGTCCTCTCCG | 26094 |
rs781542515 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72943029 | TCAGCTGCATGGAGA[A/G]GAAAAAGGTCCAGAT | 26094 |
rs781639820 | snp | A/G | 5.04808e-05 | 0.00502373 | missense, intron-variant | DCAF4 | GRCh38.p7 | 14:72958729 | TGGCCTTCTCGTCGC[A/G]GCTGGGGGGCTCCCG | 26094 |
rs781733410 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | DCAF4 | GRCh38.p7 | 14:72954425 | CCAACGTGGTGACGG[A/G]ACACCGGCAGTCCTT | 26094 |
rs781739356 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946396 | GGTAACAGAGCGAGA[C/T]CCTGTCTCAAAAAAA | 26094 |
rs781768209 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant | DCAF4 | GRCh38.p7 | 14:72954355 | GACTACATGTGACAT[A/G]ATCTTACCAGCCCAT | 26094 |
rs796086067 | snp | C/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72932335 | GTCTGATTTTGGTAA[C/T]AAGGTAATACTGGCC | 26094 |
rs796121500 | in-del | -/CTC | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72954558 | ATTGAAATTGGACTC[-/CTC]TGTGTGCCATCTAGT | 26094 |
rs796138110 | snp | A/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930365 | CCTCCACCTCCCGGG[A/T]TCAAGCGATTGTTCT | 26094 |
rs796204845 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72960173 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGTTTTAT | 26094 |
rs796243054 | in-del | -/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950819 | CTGTATGTTTTTTTT[-/T]AAACAAAAGCTGCTT | 26094 |
rs796280105 | in-del | -/CA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72946227 | GAAACCTTGTCTCTA[-/CA]AAAAAAAAAAAAAAA | 26094 |
rs796338533 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72961284 | TGGGATTAAGATTCC[A/G]CTCTTCCCAACTCTG | 26094 |
rs796349725 | in-del | -/TA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72930642 | GTGTATGTGTGTGTG[-/TA]TATATATATATGTAG | 26094 |
rs796424861 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72927964 | CCCGGCTAATTTTTA[A/G]ATTATTTGTTAAGAT | 26094 |
rs796476126 | in-del | -/A | | | intron-variant, utr-variant-5-prime | DCAF4 | GRCh38.p7 | 14:72935082 | TCATGCAGAGTGATG[-/A]GTGCAAACATGGACT | 26094 |
rs796731838 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | DCAF4 | GRCh38.p7 | 14:72960758 | CCATAGCAAAGCCTG[C/G]TTGAGGGGAAGAGGC | 26094 |
rs796741895 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72953782 | TATTTATTTATTTAT[G/T]TGTGTGTGTGTGTGT | 26094 |
rs796755359 | in-del | -/AA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72943188 | CAAACCTGGCTCTGG[-/AA]AGAAGCCAACTGCAA | 26094 |
rs796772228 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72936997 | ACTCACTTTGGCAAG[C/T]AGGTAATCAATAGCA | 26094 |
rs796820553 | snp | G/T | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72940596 | TCGATAAGTTGTTTT[G/T]TTTTTTTTTTTTGAG | 26094 |
rs796863573 | in-del | -/ATATATATATATA | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72928587 | TAGTAAACATCCTTT[-/ATATATATATATA]TATATATATATATAT | 26094 |
rs796875871 | snp | A/G | | | intron-variant | DCAF4 | GRCh38.p7 | 14:72950955 | ATTGGACTAGGGAGG[A/G]ATCAGAGAGGGCTTT | 26094 |
rs796960265 | snp | A/G | | | upstream-variant-2KB | DCAF4 | GRCh38.p7 | 14:72925143 | GGTCTGGAACTCCTA[A/G]CCTCAAGTGATCCAC | 26094 |