SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs743273 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116629 | GGTCATGTCCACAGC[A/G]TATTGGTCTTGCTCT | 80344 |
rs762093 | snp | C/G | 0.486067 | 0.0822953 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122709 | AGTTAAGGAAATGCA[C/G]TGGCTTTGAAGATTT | 80344 |
rs1134334 | snp | A/G | 0.498369 | 0.0285077 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124905 | aaaaactagccggat[A/G]tggtggcgggtgcct | 80344 |
rs1134340 | snp | C/T | 0.49263 | 0.0602539 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24125004 | tgcagtgagccaaga[C/T]catgccattacactc | 80344 |
rs2277479 | snp | A/G | 0.152001 | 0.229992 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118295 | TCCCATGATAAAGGG[A/G]AGACTCCACAGGTAC | 80344 |
rs2277480 | snp | A/G | 0.478354 | 0.101757 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118306 | AGGGAAGACTCCACA[A/G]GTACACTGAGTGGGA | 80344 |
rs2277481 | snp | A/G | 0.48546 | 0.0840147 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118336 | AGATGTCTAATCTAG[A/G]AAAGTTACAAGGAAA | 80344 |
rs2277482 | snp | C/T | 0.451982 | 0.14732 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118586 | TGGGACCTGAGGTTT[C/T]CATGTGCCTGTCCCC | 80344 |
rs2277483 | snp | A/G | 0.498503 | 0.0273153 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122683 | TTTGTGGTGCCTTCC[A/G]TATCTTACTAAAATC | 80344 |
rs3207709 | snp | A/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115581 | ACAGGACCTAAGAAT[A/G]CTGTGACCAGAAGAT | 80344 |
rs3742499 | snp | C/T | 0.142155 | 0.225543 | intron-variant | DCAF11 | GRCh38.p7 | 14:24117624 | ATATGGCTGAAGTGG[C/T]CCTCTATTTCTGCTA | 80344 |
rs3811175 | snp | A/T | 0.127944 | 0.218179 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24114255 | AGCCAGGGATTGTCT[A/T]AAAAAATTGTCAGAC | 80344 |
rs3825583 | snp | A/T | 0.257732 | 0.24988 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24114637 | CTGGCAGTTCCCACT[A/T]ACTCCTCCCCAGCAA | 80344 |
rs3825584 | snp | A/G | 0.453343 | 0.145435 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24118430 | GATATGGCCGTTTCC[A/G]TAAATTCAAGAGCAT | 80344 |
rs6573565 | snp | A/G | 0.4862 | 0.0819127 | downstream-variant-500B | DCAF11 | GRCh38.p7 | 14:24125524 | ttttaTGTTATCGAA[A/G]TAATGTAAAATGTTT | 80344 |
rs7141186 | snp | A/G | 0.0109286 | 0.0731087 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124035 | TGGGAACCTGGCTCA[A/G]TGTCTGTCTCTCTCT | 80344 |
rs7359087 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24116938 | AGTGAGGTTGGTGCA[A/G]GGAGGAGGTGCAGCA | 80344 |
rs8008888 | snp | A/G | 0.318415 | 0.240457 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116053 | GCTTGAAAAAAAAAA[A/G]GGGGGGGTCCTAGTG | 80344 |
rs8009511 | snp | A/G | 0.498369 | 0.0285077 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124771 | agtaggccgggcacg[A/G]tggttcacacctgta | 80344 |
rs8012480 | snp | A/T | 0.0444908 | 0.142359 | downstream-variant-500B | DCAF11 | GRCh38.p7 | 14:24125437 | ATTCAAATTGTTAGT[A/T]TCCTTATAGCTTCAT | 80344 |
rs10134506 | snp | C/G | 0.161596 | 0.233848 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120609 | aaTGGAAGACAATCT[C/G]ATTAAGGCTAGAATA | 80344 |
rs10138006 | snp | C/T | 0.046775 | 0.145601 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113959 | TCAACCCACACGTCC[C/T]CACCCAGCCAGGGCG | 80344 |
rs10146643 | snp | A/C | 0.497359 | 0.0362457 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120261 | TAAAAAAAAAAACAA[A/C]AAAAAAAAACTAAGG | 80344 |
rs11428836 | in-del | -/G | 0 | 0 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113293 | ATGACACGTTAGTGG[-/G]TGCAGCGCACCAGCA | 80344 |
rs11549425 | snp | C/T | 0.0501905 | 0.150254 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123777 | GTGCTGAGGAAACAC[C/T]CTTACCCATGCCCCT | 80344 |
rs11848386 | snp | A/C | 0.0391387 | 0.134304 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DCAF11, NRL | GRCh38.p7 | 14:24115054 | AGGAGGGGTGTTAGG[A/C]CAAATTCTATTTTCA | 80344 |
rs12435994 | snp | A/C | 0.498459 | 0.0277128 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120252 | CTATTTATTTAAAAA[A/C]AAAAACAAAAAAAAA | 80344 |
rs12435995 | snp | A/C | 0.498459 | 0.0277128 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120255 | TTTATTTAAAAAAAA[A/C]AACAAAAAAAAAAAA | 80344 |
rs17101347 | snp | G/T | 0.0383715 | 0.133092 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DCAF11, NRL | GRCh38.p7 | 14:24114903 | CTCGCGCCGCTGCGG[G/T]TCCTGCGACCGCTCC | 80344 |
rs17101367 | snp | C/T | 0.385689 | 0.209972 | synonymous-codon, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24118458 | CATCAAGGCCCGCGA[C/T]GTAGGCTGGAGCGTC | 80344 |
rs17101392 | snp | C/G | 0.118584 | 0.212673 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124205 | ATTTGTTCACTGAGC[C/G]TTGCAATAGGTGCTC | 80344 |
rs34097612 | in-del | -/A | | | downstream-variant-500B | DCAF11 | GRCh38.p7 | 14:24125353 | CTGCCAAGTGATAAA[-/A]GTTACCTAAGGTGCT | 80344 |
rs34426457 | snp | A/G | 0.000313995 | 0.0125259 | synonymous-codon, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24122987 | CTTCACAATGTGGCC[A/G]CTTAGAAGGTCGTAC | 80344 |
rs34701145 | in-del | -/C | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24122041 | ATGGTGGCACAGGCC[-/C]TGTAGTCCCAGCTAC | 80344 |
rs35069044 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24121386 | GAAGCTGAAGCTCCC[-/C]AGGGGACAGCTCCTT | 80344 |
rs35577926 | in-del | -/TG | 0.498369 | 0.0285077 | downstream-variant-500B | DCAF11 | GRCh38.p7 | 14:24125566 | ATACCTAGGAGATAT[-/TG]TGAGTTCATTTCCAG | 80344 |
rs35596427 | in-del | -/C | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24118587 | GGACCTGAGGTTTCC[-/C]ATGTGCCTGTCCCCT | 80344 |
rs55668591 | snp | A/G | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24122513 | AAAAAAAAAGAAAAA[A/G]AAAAAAAAAACCAGA | 80344 |
rs55963929 | in-del | -/A | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24122158 | GTGAGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 80344 |
rs56271764 | snp | A/C | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24120258 | ATTTAAAAAAAAAAA[A/C]AAAAAAAAAAAACTA | 80344 |
rs60825374 | snp | A/C | | | intron-variant | DCAF11 | GRCh38.p7 | 14:24120257 | TATTTAAAAAAAAAA[A/C]CAAAAAAAAAAAACT | 80344 |
rs61744791 | snp | A/C/G/T | 0.0139391 | 0.0823128 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24117358 | GGGCTTAGGCGGGCC[A/C/G/T]CCCAGAAGCACAGCT | 80344 |
rs73603087 | snp | A/C/G | 0.0109719 | 0.0732508 | intron-variant | DCAF11 | GRCh38.p7 | 14:24121304 | TTGCTCAGGACTGGT[A/C/G]GTACGAAACAATCCC | 80344 |
rs74040010 | snp | A/G | 0.0788843 | 0.182262 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116696 | TGGGAGGTCAACTTA[A/G]TAGGTCACGTCCACA | 80344 |
rs74040011 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116842 | AGTGGTCTAAGAGCT[A/G]GATAGCCATTGACTC | 80344 |
rs74040012 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF11 | GRCh38.p7 | 14:24119073 | GATGTGCCTTACAAC[C/T]GTTGTCAGATTTTAT | 80344 |
rs74665383 | snp | C/G | 0.5 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120534 | TACACTCCAGCCTGG[C/G]TGACAGAGCAAGACT | 80344 |
rs75570711 | snp | A/C | 0.5 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122491 | GCGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAA | 80344 |
rs75719972 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115924 | AGCTCCATACCCAGT[A/G]AGAGTGGTTCTTACC | 80344 |
rs76180205 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113390 | TAATAAAAAAAAAAA[A/T]TGATTCCGTCACATT | 80344 |
rs76629917 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113631 | TACTAATAATTTCAA[C/G]ACCGTTAACACTAGA | 80344 |
rs77478594 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF11 | GRCh38.p7 | 14:24121058 | GGAGGACCTCCCCCT[C/T]AGCCCTCTTTGCCAG | 80344 |
rs77582680 | snp | A/C | 0 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122160 | GAGAAACTGTCTCAA[A/C]AAAAAAAAAAAAAAG | 80344 |
rs77652957 | snp | A/C | 0.5 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122490 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 80344 |
rs77883085 | snp | A/G/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115405 | AAGGTTTGTGTTCCC[A/G/T]ACGCCTTGGTAGTTG | 80344 |
rs77935488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115510 | GGAGACCCTGGTATT[G/T]CTAGAGCACGCTTTG | 80344 |
rs78107024 | snp | A/G | 0.00392469 | 0.0441242 | intron-variant | DCAF11 | GRCh38.p7 | 14:24119930 | CTGTACAGCCAGGCC[A/G]CTAAGGTTCTAGTTG | 80344 |
rs78265727 | snp | C/T | 0.0158469 | 0.0875917 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124428 | TCACACTCAGAACCT[C/T]ATACCCCAGAGCAAA | 80344 |
rs78469280 | snp | A/C/G | 0.00555246 | 0.0523972 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24118471 | GACGTAGGCTGGAGC[A/C/G]TCTTGGATGTGGCCT | 80344 |
rs78584440 | snp | A/C | 0.0141658 | 0.0829593 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123320 | AGTAGATCCAACCTC[A/C]AGCCCCATATAGGGT | 80344 |
rs79254253 | snp | C/T | 0.0383715 | 0.133092 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113787 | CCTCACTGGGAGAGG[C/T]CCCAGGAGGGCCCAA | 80344 |
rs111289851 | snp | C/T | 0.5 | 0 | downstream-variant-500B | DCAF11 | GRCh38.p7 | 14:24125377 | AGGTGCTACCCATCT[C/T]ACCCAGAACCTGTGT | 80344 |
rs111512015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115359 | GCGCACTACGGTTCA[C/T]TCTTGCTTTCTTTGC | 80344 |
rs111567488 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113674 | ACATTCAGGACCCTT[C/T]TAAGCGCAGAGGCCA | 80344 |
rs111766644 | snp | A/C/G | 0.00856564 | 0.0648803 | stop-gained, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123204 | GCGTCTGTGGCAGTA[A/C/G]CGCCAGGCTGAGTAC | 80344 |
rs112317051 | snp | A/G | 0.0482946 | 0.147699 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113167 | TCTCACTCATAGGTG[A/G]GAATTGAACAATGAG | 80344 |
rs112340123 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF11 | GRCh38.p7 | 14:24121946 | TTGGGAGGCCAATGA[A/G]GGCAGATCACTTGAG | 80344 |
rs112450292 | snp | G/T | 0.5 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24119678 | TATAAGACCTAGAAA[G/T]AGGTCTTATATCCTG | 80344 |
rs112454085 | snp | C/G/T | 1.64762e-05 | 0.00287016 | intron-variant | DCAF11 | GRCh38.p7 | 14:24117060 | GTAAGAGGAAAAGCC[C/G/T]CTAATGTTGGAAGAC | 80344 |
rs112788511 | snp | A/G | 0.5 | 0 | intron-variant | DCAF11 | GRCh38.p7 | 14:24117054 | CACCTGGTAAGAGGA[A/G]AAGCCCCTAATGTTG | 80344 |
rs113086867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122444 | GCAGTGAGCCAAGAT[C/T]GCGCCACGGCACTCT | 80344 |
rs113214905 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24114042 | CATAAACCCGCAGGA[-/G]GGGGCAGGAGGGGGC | 80344 |
rs113382865 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116539 | GAATATTGTCTTCTG[C/T]GGTGGACTTCTCAGG | 80344 |
rs113395814 | snp | A/G | 3.6186e-05 | 0.00425343 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123348 | GGTGAACCTCTTGAT[A/G]AGCTCTCTGCCTCCT | 80344 |
rs113445360 | snp | C/G | 3.29473e-05 | 0.00405864 | intron-variant | DCAF11 | GRCh38.p7 | 14:24119534 | ATCATGGCTCCAGGA[C/G]CCTCCTTTATCCCTT | 80344 |
rs113595618 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115356 | GTAGCGCACTACGGT[C/T]CACTCTTGCTTTCTT | 80344 |
rs113861802 | snp | C/G | 9.93435e-05 | 0.00704712 | intron-variant | DCAF11 | GRCh38.p7 | 14:24117760 | CTTGGTGAAGAGACT[C/G]TAAGGGCCAGATAGG | 80344 |
rs113984103 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24125079 | AGCCAGATGTGGTGA[C/T]GCATGCCTGTAGTCC | 80344 |
rs117078522 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24115952 | ACCTAGGGAGGGTCA[C/T]CAAGAGGACCTGCTC | 80344 |
rs117087796 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | DCAF11, NRL | GRCh38.p7 | 14:24116504 | AGACTACAGTTGCAC[A/G]CACCACCGCACCCAG | 80344 |
rs118146993 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24114041 | AAACCCGCAGGAGGG[A/G]GCAGGAGGGGGCAGG | 80344 |
rs137897532 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124360 | GAGGTAGCCCCTGAA[C/T]GCAGAGCCTAAGAGA | 80344 |
rs137913082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DCAF11, NRL | GRCh38.p7 | 14:24115199 | GTGAAGCGCTTTCTT[C/G]CGAGAGGGATTTCGA | 80344 |
rs138016331 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118605 | GTGCCTGTCCCCTCT[A/G]AGCCAGGATCCCTCA | 80344 |
rs138347528 | snp | C/T | 0.000955723 | 0.0218391 | synonymous-codon, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24121417 | GATGACCTACCGGGG[C/T]CACGGAGTGCTGCAC | 80344 |
rs138449987 | snp | C/T | 4.94173e-05 | 0.00497053 | DCAF11 | 14 | allele_origin=T(somatic)/C(germline) | 14:24119602 | GACCGAGAACAGAAC[C/T]GGCGCACCCTTCAGG | 80344 |
rs138549012 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF11 | GRCh38.p7 | 14:24119338 | TTCTCCCAAGGTCAG[G/T]ATTTACAAGTTGCTT | 80344 |
rs138577883 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24124763 | ATACAAAAAGTAGGC[C/T]GGGCACGGTGGTTCA | 80344 |
rs138662169 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF11, NRL | GRCh38.p7 | 14:24113960 | CAACCCACACGTCCC[A/C]ACCCAGCCAGGGCGA | 80344 |
rs139297459 | snp | C/G | 0.000872793 | 0.0208754 | synonymous-codon, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24119577 | CAATGATGGCTGCCT[C/G]TATGTCTTTGACCGA | 80344 |
rs139504177 | snp | A/C/G | 0.000844958 | 0.0205372 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24117380 | AGCACAGCTTTCCTC[A/C/G]AATGTTGCACCAGGT | 80344 |
rs139790081 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120338 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 80344 |
rs139933200 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF11 | GRCh38.p7 | 14:24117577 | GTGTCCATTTCTATA[A/G]CAAGAGCAATATCTT | 80344 |
rs139960788 | snp | A/G | 0.000148359 | 0.00861149 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123036 | GCCTGTGTGCGTGAC[A/G]TCAGTTGGCACCCCT | 80344 |
rs140074757 | snp | A/G | 3.61246e-05 | 0.00424982 | missense, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123257 | CTGAGGAATGTGCCA[A/G]CGCCCCTGCCCCAGT | 80344 |
rs140077163 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120122 | GAAAAATGGAAGACC[A/G]GTCAGGTACAGCGGC | 80344 |
rs140199178 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DCAF11 | GRCh38.p7 | 14:24123967 | TTAAGGAAGTAGGTT[A/G]AAGTAGGACTCCTTC | 80344 |
rs140411068 | snp | C/G | 0.000512155 | 0.0159942 | intron-variant | DCAF11 | GRCh38.p7 | 14:24118344 | AATCTAGAAAAGTTA[C/G]AAGGAAACTGTCCCA | 80344 |
rs140555404 | snp | C/T | 6.64132e-05 | 0.00576213 | intron-variant | DCAF11 | GRCh38.p7 | 14:24120821 | TGATGCTTCACTATC[C/T]ACCTTTGGATTCATA | 80344 |
rs140993634 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF11 | GRCh38.p7 | 14:24122738 | CTGTAGCCCCTATGA[A/T]ATTTAGCTAAGGGCC | 80344 |