| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs757887987 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702757 | GGATGCTGAGCTCCT[A/G]TGCTGGGATCTCCGG | 55135 |
| rs757918994 | snp | A/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684757 | AATCCACTCCTCTTA[A/T]GATACTGTAAACTCT | 55135 |
| rs758319921 | snp | G/T | 1.64885e-05 | 0.00287123 | intron-variant, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703211 | GTGTCCTCACTGAAG[G/T]CACTGATAGACCCTC | 55135 |
| rs758338202 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703307 | TTTCCTGAGCCCACA[A/G]AGAGTGGGGACGAAG | 55135 |
| rs758338600 | snp | A/G | 3.29473e-05 | 0.00405864 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701609 | TCTCCTTCCTTGAGG[A/G]CAGCTGAGGCTTTGC | 55135 |
| rs758386953 | in-del | -/CAG | 4.94287e-05 | 0.00497111 | upstream-variant-2KB, cds-indel, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689283 | TTCCTGGTCAGAGTT[-/CAG]CAGCACCCAACCTGA | 55135 |
| rs758564460 | snp | C/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7693703 | AGCCTGGGCAAGAGA[C/G]CAAGACTTAGTCTCA | 55135 |
| rs758623071 | snp | A/G | 1.65427e-05 | 0.00287595 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703455 | AGAAAGGGCAGGGAG[A/G]AACGGAGGGAGGTGT | 55135 |
| rs758650970 | snp | A/C | | | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703410 | GTGGGGGGGCGCCAG[A/C]CTCCAGCATCCCTGA | 55135 |
| rs758704444 | snp | A/G | 8.2494e-05 | 0.00642185 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702364 | AAGCAGGGCCAGAGC[A/G]GCATCATCTCCTGCA | 55135 |
| rs758707736 | snp | C/G | 1.65312e-05 | 0.00287495 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688881 | TTTCTCTCTCCACTC[C/G]CCTGGAAACAGAGTT | 55135 |
| rs758757518 | snp | A/G | 0.00013138 | 0.00810388 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701906 | CCTCTGTACGGCCCC[A/G]GGAGCAGGTGCAGCC | 55135 |
| rs758811299 | snp | A/G | 1.65562e-05 | 0.00287712 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702870 | CTGTGACTCCTTCCT[A/G]CACAGGGCCCTGATA | 55135 |
| rs758882247 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688249 | CGGTAGGGGGAGCGT[A/G]GGCGCTTCTCGCCAA | 55135 |
| rs758895273 | in-del | -/A | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7689992 | CTTGCTCTGTCACCC[-/A]GGCTGGAGTGCTGTG | 55135 |
| rs758898596 | snp | A/G | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701467 | CTCTCAGCGTGGCCA[A/G]CAGCAGCCGGGAGAA | 55135 |
| rs758920001 | snp | A/G | 1.67632e-05 | 0.00289505 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701387 | TGGGATTACAGGCAT[A/G]AGCCACTGTGCCCGG | 55135 |
| rs758964518 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684208 | GTTTGAGACCAGCCT[A/G]GGCAACATAGTGAGA | 55135 |
| rs759020317 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7687618 | GGCAAGTAATCCGCC[G/T]GCCGGAGGAAGCAAA | 55135 |
| rs759039161 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700754 | AGGTCCCTGTCCTTC[A/G]AATGGTGGAAGGTGA | 55135 |
| rs759111012 | snp | A/G | | | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703054 | GTGTGGGACACGGAC[A/G]GGCCTGGCAATGATG | 55135 |
| rs759135662 | snp | C/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7687302 | CCAGCCCCAGCGATT[C/T]TCCCGAGCTGAAAAT | 55135 |
| rs759174078 | in-del | -/G | 9.93509e-05 | 0.00704738 | frameshift-variant, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702435 | CTACGGCCGCTCCCT[-/G]GGTCTGTATGCCTGG | 55135 |
| rs759226877 | in-del | -/C | 1.68142e-05 | 0.00289945 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688641 | TCCGCTGTGCTTCCT[-/C]CTGCAGTATGAAGAC | 55135 |
| rs759234953 | snp | A/G | 1.79981e-05 | 0.00299979 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689733 | ACTGCCTCTTCATCA[A/G]TGCTGCACATTTAAG | 55135 |
| rs759263242 | snp | C/T | | | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702498 | GCACCAAGGGGGCAT[C/T]ACCCACCTCTGCTTT | 55135 |
| rs759313714 | snp | G/T | 1.70632e-05 | 0.00292084 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703509 | TTTATGATACTAGAG[G/T]CTTCGTGTCTGTTTT | 55135 |
| rs759405865 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702313 | CCAGGAGCCATTGCC[C/T]CCTCCCCCACTTTGT | 55135 |
| rs759428765 | snp | C/T | 1.65334e-05 | 0.00287514 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688953 | AACTTTCTGAAAATA[C/T]AAGCCTTCCTGCAGA | 55135 |
| rs759455599 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703441 | TGATCACCAGGGCGA[A/G]AAAGGGCAGGGAGGA | 55135 |
| rs759563684 | snp | C/T | 3.29837e-05 | 0.00406088 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702824 | GTGACCACCAATCAG[C/T]GCATCTACTTCGATC | 55135 |
| rs759604308 | snp | A/G | 1.65121e-05 | 0.00287329 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702709 | GACATCCAGGGCTTT[A/G]GGGGTGACTCCAGGT | 55135 |
| rs759642779 | snp | C/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684235 | GAGATCCTGTCAATA[C/T]AAAAAAATAAAATAG | 55135 |
| rs759839550 | snp | A/C | 1.64806e-05 | 0.00287054 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689221 | CCCCCATCTTCCTTT[A/C]AGCGCTTGGAACTAC | 55135 |
| rs759877669 | snp | A/G | 1.65094e-05 | 0.00287305 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689074 | TGCAGAGGACGAGGG[A/G]GACACGTAAGTGGTG | 55135 |
| rs759910930 | snp | C/T | 6.58913e-05 | 0.00573945 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701654 | GCCCTTTCCTTCCCC[C/T]AGGATGAGCTGACGG | 55135 |
| rs760035612 | snp | A/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7695247 | GGCGTGAGCCACTGC[A/C]CCCGGCCTTAAATAG | 55135 |
| rs760046060 | snp | C/T | 8.24436e-05 | 0.00641989 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703279 | CCTGGCCACTGCCTC[C/T]GGTCAGCGTGTGTTT | 55135 |
| rs760086957 | snp | C/T | 3.29902e-05 | 0.00406128 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688722 | CAGCTCCAGCCCATC[C/T]TTCTCCCCACGCTTC | 55135 |
| rs760176224 | snp | A/G | 1.64885e-05 | 0.00287123 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703271 | CTGCCTCTCCTGGCC[A/G]CTGCCTCCGGTCAGC | 55135 |
| rs760176562 | snp | A/C | 8.23744e-05 | 0.0064172 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701577 | ATACTCAGCCCCAGC[A/C]CTCGTACTGGCCCGG | 55135 |
| rs760316057 | snp | C/T | 9.88338e-05 | 0.00702902 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700707 | GACTCCTTTTCCCTC[C/T]GAGTGACTCAGCCAT | 55135 |
| rs760362994 | in-del | -/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7687873 | GTCATTTTTTAGGAA[-/G]GCTTTCCGTAATATC | 55135 |
| rs760469260 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7701189 | GTTGGCCAGGCTGGT[C/T]TCGAACTGACCTCAG | 55135 |
| rs760476968 | snp | A/G | 1.6651e-05 | 0.00288535 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702469 | GATGGCTCCCCTCTC[A/G]CCTTGCTGGGAGGGC | 55135 |
| rs760537751 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700761 | TGTCCTTCGAATGGT[A/G]GAAGGTGATACCATC | 55135 |
| rs760740919 | snp | C/T | 1.65315e-05 | 0.00287498 | intron-variant, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701447 | GGGTTTCAGTGTCCA[C/T]GTCTCTCTCAGCGTG | 55135 |
| rs760828940 | snp | A/C | 1.65351e-05 | 0.00287528 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688864 | ACGGGAGGGGGACCC[A/C]GTTTCTCTCTCCACT | 55135 |
| rs760854203 | snp | A/G | 1.65021e-05 | 0.00287241 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702723 | TGGGGGTGACTCCAG[A/G]TCCTGTTCCTTGTCT | 55135 |
| rs760865157 | snp | A/C | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685405 | AATGTCAGACAGTAC[A/C]TTGAAGGACAGAAGC | 55135 |
| rs760896353 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7693025 | GGATTACAAGCATGA[A/G]CCACCGCGCCCAGCC | 55135 |
| rs760941679 | snp | C/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702839 | CGCATCTACTTCGAT[C/G]TGGACCCGTGAGTGG | 55135 |
| rs760942543 | snp | A/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700356 | TGTTTATAAAGAAAA[A/C]GTATAAGGCCCGGCA | 55135 |
| rs761067141 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7696017 | CTCCTTCTCTGATAG[A/G]TATGACGGAAGGGGA | 55135 |
| rs761113077 | snp | C/T | 3.32066e-05 | 0.00407458 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689336 | TGGTAAGGATAACAA[C/T]GGGGCAGGGAGCTGA | 55135 |
| rs761120156 | snp | A/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691261 | ACAAAACAAAAAACC[A/C]AGAATGCTGGTATAG | 55135 |
| rs761173739 | snp | C/T | 1.71469e-05 | 0.002928 | stop-gained, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701762 | ACGGCCCGGCCTGGC[C/T]GAGACTGCGAGGTCC | 55135 |
| rs761263963 | snp | A/G | 1.66266e-05 | 0.00288323 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689339 | TAAGGATAACAACGG[A/G]GCAGGGAGCTGACCA | 55135 |
| rs761304560 | snp | C/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700253 | AAGGATCAAATGGCA[C/G]CTAGCATGTACTCAG | 55135 |
| rs761413179 | snp | A/G | 1.65622e-05 | 0.00287764 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688846 | AGCTGTGTCCCAGGA[A/G]CTACGGGAGGGGGAC | 55135 |
| rs761422567 | snp | C/T | 5.05932e-05 | 0.00502932 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701851 | CACCTGCACAGGGGC[C/T]TTTTGTGAGCCGGGG | 55135 |
| rs761454111 | snp | A/T | 5.44203e-05 | 0.00521605 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688609 | AGAACTTCGAAGCCA[A/T]CCTGGCTGAGGCTAA | 55135 |
| rs761634556 | snp | G/T | 3.29679e-05 | 0.00405991 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700851 | AATGTTTGCCTCCCT[G/T]CTCGCCGCCCCACCA | 55135 |
| rs761637235 | snp | G/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685449 | GCACATAATGTATGA[G/T]TCCCCCCTTTTTTTT | 55135 |
| rs761696793 | snp | C/T | 1.64996e-05 | 0.0028722 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688732 | CCATCCTTCTCCCCA[C/T]GCTTCCCCGATGAAT | 55135 |
| rs761814385 | snp | A/G | 1.67466e-05 | 0.00289362 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702492 | GGGAGGGCACCAAGG[A/G]GGCATCACCCACCTC | 55135 |
| rs761818772 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701562 | CTGGTAGGGACCGCC[A/G]TACTCAGCCCCAGCA | 55135 |
| rs761900033 | snp | A/G | 1.98979e-05 | 0.00315413 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702602 | GGCAGCGGGGCAGGA[A/G]CAGGGATGTAGTCTG | 55135 |
| rs761911830 | snp | C/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703005 | CAGGACCGGGCAGTT[C/G]CTAGTGAGTGGCAGC | 55135 |
| rs762036489 | in-del | -/G | 1.65149e-05 | 0.00287353 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702956 | TCCTGCCCCAGGGGT[-/G]AGGCCTCTGCCAGCA | 55135 |
| rs762178428 | snp | C/T | 4.95831e-05 | 0.00497886 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702846 | ACTTCGATCTGGACC[C/T]GTGAGTGGCTGTGAC | 55135 |
| rs762610453 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703377 | TCCACCTTGAATGTC[A/G]GCTTCAGCTCTGGTG | 55135 |
| rs762638365 | snp | C/T | 1.65236e-05 | 0.00287429 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703420 | GCCAGACTCCAGCAT[C/T]CCTGATGATCACCAG | 55135 |
| rs762717799 | snp | G/T | | | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688807 | GGATCCGCCCCGGTT[G/T]TCCCCAGATCCTGTG | 55135 |
| rs762768775 | snp | C/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7687066 | AGGGATTCCCTACGC[C/G]CAGCACCGGGTGGAT | 55135 |
| rs762845872 | snp | G/T | 1.65578e-05 | 0.00287726 | intron-variant, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701434 | TTTGACAGCACCGGG[G/T]TTTCAGTGTCCATGT | 55135 |
| rs762966384 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7696901 | GCACTGTCCACCAGG[C/T]AGTTGGATATATGGG | 55135 |
| rs762994587 | in-del | -/AAAT | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698875 | GCGAGACTCCGTCAA[-/AAAT]AAATAAATAAATAAA | 55135 |
| rs763023897 | snp | C/T | 1.65176e-05 | 0.00287376 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688759 | GAATAAAAATGCGGA[C/T]TCTGAACTGATGCCA | 55135 |
| rs763059880 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698516 | GTGGCTGGATTGCTT[A/G]AGGCCAGGAGTTTTA | 55135 |
| rs763211473 | snp | A/G | 1.65337e-05 | 0.00287517 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689057 | ACCTCTGGGGAACCC[A/G]CTGCAGAGGACGAGG | 55135 |
| rs763258702 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701570 | GACCGCCATACTCAG[C/T]CCCAGCACTCGTACT | 55135 |
| rs763584318 | in-del | -/TGTG | 1.64867e-05 | 0.00287107 | frameshift-variant, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703038 | GAGCGGGGCTGTCTC[-/TGTG]TGGGACACGGACGGG | 55135 |
| rs763586018 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | WRAP53 | GRCh38.p7 | 17:7703192 | TGAATCCCAGAGGGA[A/G]CAAGTGTCCTCACTG | 55135 |
| rs763725445 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7690291 | TATATGTTAGTCACT[A/G]TGCTGGGATAAAGTG | 55135 |
| rs763768243 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698838 | CCAAGATTGTGCCAC[C/T]GCATTCCAGCCTGGG | 55135 |
| rs763828661 | snp | A/G | 3.2981e-05 | 0.00406071 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703280 | CTGGCCACTGCCTCC[A/G]GTCAGCGTGTGTTTC | 55135 |
| rs763839659 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700765 | CTTCGAATGGTGGAA[A/G]GTGATACCATCTATG | 55135 |
| rs763850180 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700158 | GGTTCAAGGGATTCT[C/T]CTGCCTCAGCCTCCT | 55135 |
| rs764037927 | snp | A/G | 1.65348e-05 | 0.00287526 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688865 | CGGGAGGGGGACCCA[A/G]TTTCTCTCTCCACTC | 55135 |
| rs764102509 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700719 | CTCCGAGTGACTCAG[C/T]CATTCCCCCGTCTCT | 55135 |
| rs764119462 | snp | G/T | 1.65302e-05 | 0.00287486 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702327 | CCCCTCCCCCACTTT[G/T]TTCCTTCCCTCTCTA | 55135 |
| rs764127676 | snp | A/C | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684441 | TGGTAGCCCTATACT[A/C]CAACTGTAAAATAAT | 55135 |
| rs764152004 | snp | A/G | 1.67024e-05 | 0.0028898 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702481 | CTCGCCTTGCTGGGA[A/G]GGCACCAAGGGGGCA | 55135 |
| rs764296379 | snp | A/G | 3.30191e-05 | 0.00406306 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702842 | ATCTACTTCGATCTG[A/G]ACCCGTGAGTGGCTG | 55135 |
| rs764309128 | snp | C/G | 1.65233e-05 | 0.00287426 | intron-variant, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701452 | TCAGTGTCCATGTCT[C/G]TCTCAGCGTGGCCAG | 55135 |
| rs764437508 | in-del | -/CT | 9.92868e-05 | 0.00704511 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688665 | TGAAGACTTTGGAGA[-/CT]CAACCGTTAGCTCCG | 55135 |
| rs764490879 | snp | C/T | 1.64974e-05 | 0.00287201 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702727 | GGTGACTCCAGGTCC[C/T]GTTCCTTGTCTCCAG | 55135 |
| rs764681311 | snp | A/T | 1.64762e-05 | 0.00287016 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689234 | TTCAGCGCTTGGAAC[A/T]ACAGCTTCTCCCAGC | 55135 |
| rs764697968 | snp | A/G/T | 3.32376e-05 | 0.00407651 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689338 | GTAAGGATAACAACG[A/G/T]GGCAGGGAGCTGACC | 55135 |
| rs764895538 | snp | A/G | 1.71437e-05 | 0.00292772 | missense, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701763 | CGGCCCGGCCTGGCC[A/G]AGACTGCGAGGTCCG | 55135 |
| rs764972008 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700336 | TTTGTTTCTTCCTCT[C/T]TAAGTGTTTATAAAG | 55135 |
| rs764981522 | snp | A/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684298 | TCGTGAGGCTGCTAG[A/T]GGACTGCTTGAGCCC | 55135 |
| rs765007219 | snp | G/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685753 | GATTCCATTCTATAT[G/T]AAGTTCTCCAACAGG | 55135 |
| rs765073967 | snp | A/G | 1.65015e-05 | 0.00287237 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688733 | CATCCTTCTCCCCAC[A/G]CTTCCCCGATGAATA | 55135 |
| rs765076522 | snp | A/C | 1.64874e-05 | 0.00287113 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703304 | GTGTTTCCTGAGCCC[A/C]CAGAGAGTGGGGACG | 55135 |
| rs765264100 | snp | C/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700768 | CGAATGGTGGAAGGT[C/G]ATACCATCTATGATT | 55135 |
| rs765268037 | snp | A/C | 1.76216e-05 | 0.00296825 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688623 | ATCCTGGCTGAGGCT[A/C]ATCTCCGCTGTGCTT | 55135 |
| rs765444563 | snp | C/T | 1.65318e-05 | 0.002875 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688878 | CAGTTTCTCTCTCCA[C/T]TCCCCTGGAAACAGA | 55135 |
| rs765455464 | snp | C/G | 3.48402e-05 | 0.00417359 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703530 | TGTCTGTTTTGGGGG[C/G]GCATATGAGTGAGGT | 55135 |
| rs765462600 | snp | A/C | 0.000165459 | 0.00909407 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688972 | CCTTCCTGCAGAAGA[A/C]GCAAACGGGAGCCTT | 55135 |
| rs765587386 | snp | G/T | 1.65422e-05 | 0.0028759 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703452 | GCGAGAAAGGGCAGG[G/T]AGGAACGGAGGGAGG | 55135 |
| rs765624214 | in-del | -/GG | 1.65157e-05 | 0.0028736 | upstream-variant-2KB, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689071 | CGCTGCAGAGGACGA[-/GG]GAGACACGTAAGTGG | 55135 |
| rs765650726 | snp | A/T | 3.29707e-05 | 0.00406008 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689610 | CTGACGGTTCCTGCA[A/T]CTTGACCAATAGTGC | 55135 |
| rs765683390 | snp | C/G | 3.30589e-05 | 0.00406551 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702855 | TGGACCCGTGAGTGG[C/G]TGTGACTCCTTCCTA | 55135 |
| rs765684795 | in-del | -/CT | 0.444444 | 0.157135 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702980 | GCCAGCAAATCTCTC[-/CT]CTCTCTCGCAGGACC | 55135 |
| rs765684862 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703022 | TAGTGAGTGGCAGCA[C/T]GAGCGGGGCTGTCTC | 55135 |
| rs765912726 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7693663 | AGGCGAAGGTTGCAG[C/T]GAGCTGATCGCACCA | 55135 |
| rs766017619 | snp | C/T | 1.67764e-05 | 0.00289619 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689352 | GGGGCAGGGAGCTGA[C/T]CACCCCCGAGATTTT | 55135 |
| rs766017748 | snp | G/T | 7.40494e-05 | 0.00608434 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701866 | CTTTTGTGAGCCGGG[G/T]GCCACCTGTGGGGGT | 55135 |
| rs766025788 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686058 | GAGCTAAGAGATGGG[A/G]CAGCGGGAGAAATGA | 55135 |
| rs766034158 | snp | C/T | 1.64866e-05 | 0.00287106 | stop-gained, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689639 | GCTGATAACATCTTG[C/T]GAATTTATAACCTGC | 55135 |
| rs766212187 | snp | C/G | 7.33514e-05 | 0.0060556 | missense, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701777 | CGAGACTGCGAGGTC[C/G]GAGCCACATTTGGTA | 55135 |
| rs766320139 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7696915 | GCAGTTGGATATATG[A/G]GTTCAGAGTATAGAG | 55135 |
| rs766375350 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703385 | GAATGTCGGCTTCAG[C/T]TCTGGTGGTGTGGGG | 55135 |
| rs766422100 | snp | A/G | 4.96134e-05 | 0.00498039 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688853 | TCCCAGGAGCTACGG[A/G]AGGGGGACCCAGTTT | 55135 |
| rs766435850 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698529 | TTGAGGCCAGGAGTT[C/T]TAGACCAGCGTGAGC | 55135 |
| rs766557841 | in-del | -/G/GG | 0.00495924 | 0.0495588 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703396 | CAGCTCTGGTGGTGT[-/G/GG]GGGGGGGCGCCAGAC | 55135 |
| rs766567403 | snp | C/T | 3.50128e-05 | 0.00418392 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703532 | TCTGTTTTGGGGGGG[C/T]ATATGAGTGAGGTGG | 55135 |
| rs766610610 | snp | A/G | 1.65255e-05 | 0.00287445 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689063 | GGGGAACCCGCTGCA[A/G]AGGACGAGGGAGACA | 55135 |
| rs766656480 | snp | A/G | | | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7702266 | TGTTGGTGCTGGGAC[A/G]GGAGACAGACCTCTG | 55135 |
| rs766695794 | snp | A/G | 1.65485e-05 | 0.00287645 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688983 | AAGAAGCAAACGGGA[A/G]CCTTTCTGAAGAAGA | 55135 |
| rs766808723 | snp | A/C | 1.64762e-05 | 0.00287016 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701572 | CCGCCATACTCAGCC[A/C]CAGCACTCGTACTGG | 55135 |
| rs766817615 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701520 | TTCACTGGAGAGCTC[C/T]GGGCTTCCTTTCGCG | 55135 |
| rs767000103 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7690643 | AAGGCCCTGCATGGT[A/G]GCTCACGCCTGTAAT | 55135 |
| rs767018726 | snp | A/T | 1.64857e-05 | 0.00287099 | intron-variant | WRAP53 | GRCh38.p7 | 17:7703150 | GTTCAATTCCAGAGA[A/T]GTTGGGGCTTGGGTT | 55135 |
| rs767182183 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | WRAP53 | GRCh38.p7 | 17:7703164 | ATGTTGGGGCTTGGG[C/T]TGGGGAGGGAGGTGA | 55135 |
| rs767255046 | snp | A/C/T | 4.96186e-05 | 0.00498069 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702314 | CAGGAGCCATTGCCC[A/C/T]CTCCCCCACTTTGTT | 55135 |
| rs767311232 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703056 | GTGGGACACGGACGG[A/G]CCTGGCAATGATGGG | 55135 |
| rs767383199 | snp | C/G | 1.65111e-05 | 0.0028732 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689658 | TTTATAACCTGCCCC[C/G]AGAGCTGTACCATGA | 55135 |
| rs767445901 | in-del | -/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7692029 | TTTTTTAGTAGAGAT[-/G]GGGGGGTTCATCATA | 55135 |
| rs767462997 | snp | C/G | 1.65373e-05 | 0.00287548 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688957 | TTCTGAAAATACAAG[C/G]CTTCCTGCAGAAGAA | 55135 |
| rs767511908 | snp | A/G | 0.000193855 | 0.00984326 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701880 | GGGCCACCTGTGGGG[A/G]TTCACGCCGTCCTCT | 55135 |
| rs767536819 | snp | A/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684286 | AATCCCAGCTACTCG[A/T]GAGGCTGCTAGAGGA | 55135 |
| rs767653415 | snp | G/T | 1.65089e-05 | 0.00287301 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702712 | ATCCAGGGCTTTGGG[G/T]GTGACTCCAGGTCCT | 55135 |
| rs767714126 | snp | C/T | 3.47614e-05 | 0.00416887 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702529 | CATCCCGATGGCAAC[C/T]GCTTCTTCTCAGGAG | 55135 |
| rs767803897 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700778 | AAGGTGATACCATCT[A/G]TGATTACTGCTGGTA | 55135 |
| rs767921886 | snp | A/G | 1.65078e-05 | 0.00287291 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689075 | GCAGAGGACGAGGGA[A/G]ACACGTAAGTGGTGA | 55135 |
| rs768089496 | snp | A/C/G | 9.89257e-05 | 0.00703236 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703361 | CTCTCCACGCGCCAC[A/C/G]TCCACCTTGAATGTC | 55135 |
| rs768131332 | snp | C/T | 3.29506e-05 | 0.00405884 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701580 | CTCAGCCCCAGCACT[C/T]GTACTGGCCCGGCTC | 55135 |
| rs768151603 | snp | C/G | 9.8837e-05 | 0.00702914 | splice-acceptor-variant | WRAP53 | GRCh38.p7 | 17:7701656 | CCTTTCCTTCCCCCA[C/G]GATGAGCTGACGGCA | 55135 |
| rs768364856 | snp | C/T | 0.00013197 | 0.00812203 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688725 | CTCCAGCCCATCCTT[C/T]TCCCCACGCTTCCCC | 55135 |
| rs768411006 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702771 | TGTGCTGGGATCTCC[A/G]GCAGTCTGGTTACCC | 55135 |
| rs768426584 | snp | G/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7702617 | GCAGGGATGTAGTCT[G/T]CAGTGTAGGGGAATG | 55135 |
| rs768560508 | snp | C/T | 1.65214e-05 | 0.0028741 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689184 | CCTCTGCCCCCTTTG[C/T]TTGGCGACCCAGGTT | 55135 |
| rs768615197 | snp | C/T | 8.0064e-05 | 0.00632658 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702592 | AAAGCAGCTGGGCAG[C/T]GGGGCAGGAGCAGGG | 55135 |
| rs768640535 | snp | G/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7701276 | ACCCAGCCTCATTTT[G/T]GTATTTTTAGTAGAG | 55135 |
| rs768679162 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701504 | TCATATCTGGGACGC[A/G]TTCACTGGAGAGCTC | 55135 |
| rs768680892 | snp | G/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703111 | CTGCCCCAGAAGGAC[G/T]GCACCAATGGCGTGA | 55135 |
| rs768865976 | snp | C/T | 0.000144791 | 0.00850733 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701926 | CAGGTGCAGCCCAGT[C/T]GGCAGAGGAGCAAAC | 55135 |
| rs768877660 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685150 | AACTCAGAGCTTCTG[-/A]AAAAAGTTCAAAATA | 55135 |
| rs768895323 | snp | C/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686718 | CAATAACAGGGCTGC[C/T]GGGCCTCTCAGATTG | 55135 |
| rs768980776 | snp | A/G | 1.71773e-05 | 0.00293059 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689706 | ATGCAGAAATGGTAA[A/G]GACTGGGGCTAACTG | 55135 |
| rs769071501 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7696072 | AAAGAGGAACAGGGG[C/T]GCCTTGCTTAGCTGG | 55135 |
| rs769080565 | snp | G/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698209 | CAGTAATTTTACTCT[G/T]CAGCAGAAACTGTAG | 55135 |
| rs769107489 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689603 | AGGGCTCCTGACGGT[C/T]CCTGCATCTTGACCA | 55135 |
| rs769163565 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698041 | TGACTAATTTTTTAA[C/T]TTTTTGTAAAACTGG | 55135 |
| rs769202794 | snp | G/T | | | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703403 | TGGTGGTGTGGGGGG[G/T]CGCCAGACTCCAGCA | 55135 |
| rs769334931 | snp | C/G | 5.96321e-05 | 0.00546008 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701858 | ACAGGGGCCTTTTGT[C/G]AGCCGGGGGCCACCT | 55135 |
| rs769637437 | snp | C/G | 1.65258e-05 | 0.00287448 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688922 | AGTGAGTTGAGTCCT[C/G]GAATCGAGGAGCAAG | 55135 |
| rs769658760 | in-del | -/TCGCTCTGCTTCTCCCCGGATGGC | 1.64743e-05 | 0.00287 | cds-indel, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701678 | CTGACGGCAGCCCAT[-/TCGCTCTGCTTCTCCCCGGATGGC]TCCCAGCTCTTCTGT | 55135 |
| rs769738297 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703778 | TCTCACTCCCAAGGT[G/T]GGGGCGGCAGGGGTC | 55135 |
| rs769767639 | snp | C/T | 3.30202e-05 | 0.00406313 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702696 | CGAGGGAGGCAGGGA[C/T]ATCCAGGGCTTTGGG | 55135 |
| rs769786248 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686973 | GATGCCATGGGCTCT[A/G]AAATATACAGCTATG | 55135 |
| rs769878433 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701623 | GGCAGCTGAGGCTTT[C/G]CAAGACCTGTTTTCA | 55135 |
| rs769905168 | snp | A/G | 3.29696e-05 | 0.00406001 | intron-variant | WRAP53 | GRCh38.p7 | 17:7703134 | TGGCGTGAGGTCCTC[A/G]GTTCAATTCCAGAGA | 55135 |
| rs769925717 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701564 | GGTAGGGACCGCCAT[A/G]CTCAGCCCCAGCACT | 55135 |
| rs769948290 | in-del | -/CAAA | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691240 | AAACAAACAAACAAA[-/CAAA]CAAACACAAAACAAA | 55135 |
| rs769954174 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698332 | GTTTGAATATATTCA[C/T]GAGTAGAGTACTATA | 55135 |
| rs770005848 | snp | A/C/G | 3.29453e-05 | 0.00405854 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700737 | TTCCCCCGTCTCTGT[A/C/G]TAGGTCCCTGTCCTT | 55135 |
| rs770017809 | in-del | -/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691247 | ACAAACAAACAAACA[-/C]AAAACAAAAAACCCA | 55135 |
| rs770072513 | snp | A/C | 0.000282718 | 0.0118861 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703248 | TCTCCCTCAGCCTGC[A/C]CCCTAGCCTGCCTCT | 55135 |
| rs770273614 | snp | A/G | 0.00016419 | 0.00905915 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701962 | CAGAGCAGGTAGGAA[A/G]CCTTCCCAAGGCCAA | 55135 |
| rs770311262 | in-del | -/C | 8.2672e-05 | 0.00642877 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702311 | TGCCAGGAGCCATTG[-/C]CCCCTCCCCCACTTT | 55135 |
| rs770312151 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698150 | GGGAAAGAAATTGAC[A/G]TTATAGTATCTTACA | 55135 |
| rs770340314 | snp | A/C/T | 7.04219e-05 | 0.00593354 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689719 | AAGGACTGGGGCTAA[A/C/T]TGCCTCTTCATCAAT | 55135 |
| rs770524963 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703961 | AGGAGCACTCTCCTC[C/T]GCTCCCCGGGGCTCC | 55135 |
| rs770580910 | snp | A/G | 1.65293e-05 | 0.00287479 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688936 | TCGAATCGAGGAGCA[A/G]GAACTTTCTGAAAAT | 55135 |
| rs770582241 | snp | A/C | 1.65509e-05 | 0.00287666 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702298 | TTAGCCTGGTTAGTG[A/C]CAGGAGCCATTGCCC | 55135 |
| rs770583524 | snp | A/G | 1.65457e-05 | 0.00287621 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689020 | CGGGCCAGAGTTGGG[A/G]TCTGGAAAAGCCATG | 55135 |
| rs770702954 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7690138 | AGTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT | 55135 |
| rs770706285 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701555 | CAACCACCTGGTAGG[A/G]ACCGCCATACTCAGC | 55135 |
| rs770755456 | snp | A/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700907 | GAGAGTCAAGGGCTG[A/C]CAGGGGTCTTTGGAG | 55135 |
| rs770992500 | snp | A/C | 1.64776e-05 | 0.00287028 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689288 | TGGTCAGAGTTCAGC[A/C]CCCAACCTGAGAACT | 55135 |
| rs771063284 | snp | C/T | 1.64871e-05 | 0.00287111 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689209 | CAGGTTTATTGTCCC[C/T]CATCTTCCTTTCAGC | 55135 |
| rs771149476 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684165 | GCACTTTGGGAGGCC[A/G]AGATGGGATGAAAGC | 55135 |
| rs771403969 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700750 | GTATAGGTCCCTGTC[C/T]TTCGAATGGTGGAAG | 55135 |
| rs771431030 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700821 | CTCAGCCCAGCCAGA[C/T]ACCTCCTAGTAAGTA | 55135 |
| rs771464995 | snp | A/C/G | 3.29784e-05 | 0.00406058 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703259 | CTGCACCCTAGCCTG[A/C/G]CTCTCCTGGCCACTG | 55135 |
| rs771498263 | in-del | -/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700979 | GCTTCCTCCCCTTCC[-/T]TTTTTTTTTTTTAGA | 55135 |
| rs771625301 | snp | C/T | 1.88859e-05 | 0.00307288 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702566 | AGGTAGGGGTCACAC[C/T]CTGAGAGCCCAAAGC | 55135 |
| rs771653397 | in-del | -/CT | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7702716 | GGGCTTTGGGGGTGA[-/CT]CTCCAGGTCCTGTTC | 55135 |
| rs771854905 | snp | A/G | 4.95389e-05 | 0.00497664 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689120 | GGAGTCTGGGGAGAT[A/G]AAGTGTGAGGTCGAT | 55135 |
| rs771911772 | snp | A/C | 1.65433e-05 | 0.002876 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689038 | TGGAAAAGCCATGGA[A/C]GATACCTCTGGGGAA | 55135 |
| rs771996184 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686084 | AATGAATTCGAGTTC[C/G]GCCTCCTACCAGGAA | 55135 |
| rs772070950 | in-del | -/CCGAGACTGCGAGGT | | | cds-indel, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701761 | CACGGCCCGGCCTGG[-/CCGAGACTGCGAGGT]CCGAGCCACATTTGG | 55135 |
| rs772153861 | snp | A/G | 1.72264e-05 | 0.00293477 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703516 | TACTAGAGTCTTCGT[A/G]TCTGTTTTGGGGGGG | 55135 |
| rs772376138 | snp | C/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686544 | AAAAAGAAATGCAGG[C/G]GGAGAATAGCAGCCT | 55135 |
| rs772397891 | snp | C/T | 3.7701e-05 | 0.00434155 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701840 | AAGGGCACTGCCACC[C/T]GCACAGGGGCCTTTT | 55135 |
| rs772450459 | snp | C/G | 1.6489e-05 | 0.00287128 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703276 | TCTCCTGGCCACTGC[C/G]TCCGGTCAGCGTGTG | 55135 |
| rs772472680 | snp | A/C | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7694182 | ATGATTATAATATTA[A/C]AACATTTTAAAAAAT | 55135 |
| rs772485427 | snp | C/T | 4.99679e-05 | 0.00499815 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689570 | GTCTGGCCAGCTTTC[C/T]AACTCTCCCCTGTTT | 55135 |
| rs772549847 | snp | A/G | 1.64893e-05 | 0.0028713 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688701 | GCTGTCCTTCAGACC[A/G]GGACCCAGCTCCAGC | 55135 |
| rs772594346 | snp | A/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7695801 | TCCCAAATCCCATCA[A/T]GTCTGCCTAATCTTC | 55135 |
| rs772621341 | snp | C/G | 0.00458498 | 0.0476599 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688828 | AGATCCTGTGGCTGG[C/G]TCAGCTGTGTCCCAG | 55135 |
| rs772776812 | snp | A/T | 5.25472e-05 | 0.00512551 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701995 | AGCTGGTCAAAGGAC[A/T]GCTTCCTTCCTGAAC | 55135 |
| rs772815432 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703406 | TGGTGTGGGGGGGCG[C/G]CAGACTCCAGCATCC | 55135 |
| rs772817908 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686983 | GCTCTAAAATATACA[A/G]CTATGAGTTCTCAAT | 55135 |
| rs772838096 | snp | A/T | | | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702778 | GGATCTCCGGCAGTC[A/T]GGTTACCCACTGTGG | 55135 |
| rs772847669 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689617 | TTCCTGCATCTTGAC[C/T]AATAGTGCTGATAAC | 55135 |
| rs772914125 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7695244 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCTTAAA | 55135 |
| rs772970455 | in-del | -/GGGAG | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699345 | GAATTGCTTGAACCT[-/GGGAG]GGGAGGTGGAGGTTG | 55135 |
| rs773082754 | snp | A/C | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686319 | TTTTTTTTTTTCCTC[A/C]GGGAAGATGAGATAT | 55135 |
| rs773111498 | snp | A/G | 4.97162e-05 | 0.00498554 | intron-variant, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701431 | TCCTTTGACAGCACC[A/G]GGGTTTCAGTGTCCA | 55135 |
| rs773134577 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701630 | GAGGCTTTGCAAGAC[C/G]TGTTTTCAGCCCTTT | 55135 |
| rs773199225 | snp | A/G | 1.65468e-05 | 0.00287631 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688851 | TGTCCCAGGAGCTAC[A/G]GGAGGGGGACCCAGT | 55135 |
| rs773235897 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700855 | TTTGCCTCCCTGCTC[A/G]CCGCCCCACCACCCA | 55135 |
| rs773340183 | snp | A/G | 1.64969e-05 | 0.00287196 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689201 | TGGCGACCCAGGTTT[A/G]TTGTCCCCCATCTTC | 55135 |
| rs773357454 | snp | G/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698423 | CAGAGGGATGTATAT[G/T]ATATAATACCATTAC | 55135 |
| rs773435838 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701569 | GGACCGCCATACTCA[A/G]CCCCAGCACTCGTAC | 55135 |
| rs773508115 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684117 | AAAATAGCACTAAGA[A/G]GTCAGGCATGGTGGC | 55135 |
| rs773634281 | snp | C/G | 1.64852e-05 | 0.00287094 | intron-variant | WRAP53 | GRCh38.p7 | 17:7703135 | GGCGTGAGGTCCTCA[C/G]TTCAATTCCAGAGAT | 55135 |
| rs773685166 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700857 | TGCCTCCCTGCTCGC[C/T]GCCCCACCACCCAGT | 55135 |
| rs773820387 | snp | A/T | 1.79641e-05 | 0.00299696 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689732 | AACTGCCTCTTCATC[A/T]ATGCTGCACATTTAA | 55135 |
| rs773825543 | snp | A/C | 1.65296e-05 | 0.00287481 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702307 | TTAGTGCCAGGAGCC[A/C]TTGCCCCCTCCCCCA | 55135 |
| rs773848437 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691198 | TGGGTGACAGAGTGA[A/G]ACTCCATCCCAAAAC | 55135 |
| rs773876412 | snp | C/T | | | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689136 | AAGTGTGAGGTCGAT[C/T]TGTCCTCTGGTCCTG | 55135 |
| rs773908331 | snp | C/T | 3.29451e-05 | 0.00405851 | stop-gained, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700753 | TAGGTCCCTGTCCTT[C/T]GAATGGTGGAAGGTG | 55135 |
| rs773916846 | in-del | -/C | 0.000148673 | 0.00862058 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702338 | CTTTGTTCCTTCCCT[-/C]TCTAGCAAAAAAGCA | 55135 |
| rs773992093 | snp | A/G | | | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688997 | AGCCTTTCTGAAGAA[A/G]AAGCGAACGGGCCAG | 55135 |
| rs774018085 | snp | C/G | 0.000203504 | 0.0100852 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703506 | GTTTTTATGATACTA[C/G]AGTCTTCGTGTCTGT | 55135 |
| rs774058987 | snp | A/G | 1.65444e-05 | 0.00287609 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689033 | GGGTCTGGAAAAGCC[A/G]TGGAAGATACCTCTG | 55135 |
| rs774095773 | snp | C/T | 1.65362e-05 | 0.00287538 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688861 | GCTACGGGAGGGGGA[C/T]CCAGTTTCTCTCTCC | 55135 |
| rs774180657 | snp | C/T | 4.95872e-05 | 0.00497907 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703438 | TGATGATCACCAGGG[C/T]GAGAAAGGGCAGGGA | 55135 |
| rs774300170 | snp | C/G | 1.65105e-05 | 0.00287315 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702705 | CAGGGACATCCAGGG[C/G]TTTGGGGGTGACTCC | 55135 |
| rs774333583 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698539 | GAGTTTTAGACCAGC[A/G]TGAGCAACACAGACC | 55135 |
| rs774374559 | snp | C/T | 1.65315e-05 | 0.00287498 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688945 | GGAGCAAGAACTTTC[C/T]GAAAATACAAGCCTT | 55135 |
| rs774463771 | snp | G/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684224 | GGCAACATAGTGAGA[G/T]CCTGTCAATACAAAA | 55135 |
| rs774466254 | snp | C/G | 1.64792e-05 | 0.00287042 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689294 | GAGTTCAGCACCCAA[C/G]CTGAGAACTTCTTGA | 55135 |
| rs774508120 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699966 | TTGAACTCCTGGGCT[C/T]AAGTGATCTGCCTGC | 55135 |
| rs774574319 | snp | A/C | 3.29712e-05 | 0.00406011 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689211 | GGTTTATTGTCCCCC[A/C]TCTTCCTTTCAGCGC | 55135 |
| rs774604831 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685218 | TAAGTATTTCTCCAA[A/G]AAACACGAAAACATA | 55135 |
| rs774657140 | snp | C/T | 4.95847e-05 | 0.00497895 | missense, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701735 | TTCAACCGGACTGTG[C/T]GTGTTTTTTCCACGG | 55135 |
| rs774921033 | snp | C/T | 4.94189e-05 | 0.00497062 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701652 | CAGCCCTTTCCTTCC[C/T]CCAGGATGAGCTGAC | 55135 |
| rs774927214 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7690682 | CTCAGGAGGCCGAGG[C/T]GTGCAGATCACTTGA | 55135 |
| rs774944601 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700757 | TCCCTGTCCTTCGAA[C/T]GGTGGAAGGTGATAC | 55135 |
| rs775000135 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691885 | TCTGTTGTCCAGGCT[A/G]GAGTGCAGTGGCACC | 55135 |
| rs775038177 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700822 | TCAGCCCAGCCAGAC[A/G]CCTCCTAGTAAGTAA | 55135 |
| rs775043934 | snp | C/T | 1.6492e-05 | 0.00287154 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688718 | GACCCAGCTCCAGCC[C/T]ATCCTTCTCCCCACG | 55135 |
| rs775066741 | snp | C/G | 1.64887e-05 | 0.00287125 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703278 | TCCTGGCCACTGCCT[C/G]CGGTCAGCGTGTGTT | 55135 |
| rs775125866 | in-del | -/CTC | 3.30131e-05 | 0.00406269 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702717 | GGGCTTTGGGGGTGA[-/CTC]CAGGTCCTGTTCCTT | 55135 |
| rs775212492 | snp | C/T | 4.99372e-05 | 0.00499661 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702468 | TGATGGCTCCCCTCT[C/T]GCCTTGCTGGGAGGG | 55135 |
| rs775352941 | snp | A/G | 1.65419e-05 | 0.00287588 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689042 | AAAGCCATGGAAGAT[A/G]CCTCTGGGGAACCCG | 55135 |
| rs775499227 | snp | A/G | 1.65318e-05 | 0.002875 | intron-variant, missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701446 | GGGGTTTCAGTGTCC[A/G]TGTCTCTCTCAGCGT | 55135 |
| rs775605853 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700111 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 55135 |
| rs775614552 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702988 | ATCTCTCCTCTCTCT[C/T]GCAGGACCGGGCAGT | 55135 |
| rs775640979 | snp | C/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7685345 | ACAATCGATGGACTA[C/T]ACTAAATGAAAAGGA | 55135 |
| rs775784125 | snp | A/C | 1.64936e-05 | 0.00287168 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689599 | TTCTAGGGCTCCTGA[A/C]GGTTCCTGCATCTTG | 55135 |
| rs776051850 | snp | A/T | 6.62361e-05 | 0.00575445 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689330 | TGTAAGTGGTAAGGA[A/T]AACAACGGGGCAGGG | 55135 |
| rs776077808 | snp | C/T | 0.000164984 | 0.00908101 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688729 | AGCCCATCCTTCTCC[C/T]CACGCTTCCCCGATG | 55135 |
| rs776090557 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701657 | CTTTCCTTCCCCCAG[C/G]ATGAGCTGACGGCAG | 55135 |
| rs776212278 | snp | A/G | 1.67978e-05 | 0.00289804 | missense, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701754 | TTTTTTCCACGGCCC[A/G]GCCTGGCCGAGACTG | 55135 |
| rs776230205 | in-del | -/GAAA | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698886 | TCAAAAATAAATAAA[-/GAAA]TAAATAAATAAATAA | 55135 |
| rs776247946 | snp | C/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7701422 | TCCTCCCCTTCCTTT[C/G]ACAGCACCGGGGTTT | 55135 |
| rs776365863 | snp | A/G | 1.66629e-05 | 0.00288638 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701405 | CCACTGTGCCCGGCC[A/G]TTCCTCCCCTTCCTT | 55135 |
| rs776366967 | snp | C/T | 1.65641e-05 | 0.00287781 | upstream-variant-2KB, stop-gained, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688841 | GGCTCAGCTGTGTCC[C/T]AGGAGCTACGGGAGG | 55135 |
| rs776402169 | snp | C/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7687041 | CAATGCTTTGTGCAT[C/G]TTTTATTTCAGGGAT | 55135 |
| rs776523380 | in-del | -/AAA | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698884 | CCGTCAAAAATAAAT[-/AAA]TAAATAAATAAATAA | 55135 |
| rs776553040 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703118 | AGAAGGACTGCACCA[A/G]TGGCGTGAGGTCCTC | 55135 |
| rs776628490 | snp | A/T | 1.65403e-05 | 0.00287574 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688963 | AAATACAAGCCTTCC[A/T]GCAGAAGAAGCAAAC | 55135 |
| rs776637813 | snp | A/T | 1.64814e-05 | 0.00287061 | intron-variant | WRAP53 | GRCh38.p7 | 17:7700850 | TAATGTTTGCCTCCC[A/T]GCTCGCCGCCCCACC | 55135 |
| rs776674391 | snp | C/G | 0.000116909 | 0.00764467 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702483 | CGCCTTGCTGGGAGG[C/G]CACCAAGGGGGCATC | 55135 |
| rs776678806 | snp | G/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7702634 | AGTGTAGGGGAATGG[G/T]TGGGGATGGGGAAAA | 55135 |
| rs776760980 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701561 | CCTGGTAGGGACCGC[C/T]ATACTCAGCCCCAGC | 55135 |
| rs776832907 | snp | A/C/G | 4.94575e-05 | 0.00497259 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689609 | CCTGACGGTTCCTGC[A/C/G]TCTTGACCAATAGTG | 55135 |
| rs776914583 | snp | C/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7698057 | TTTTTGTAAAACTGG[C/G]GTCTTGCTATATTGC | 55135 |
| rs776958207 | snp | C/G | 4.69164e-05 | 0.00484314 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701850 | CCACCTGCACAGGGG[C/G]CTTTTGTGAGCCGGG | 55135 |
| rs777324261 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7697520 | AAAAATTAGCCGGGC[A/G]TGGTGGCAAATGCCT | 55135 |
| rs777396668 | snp | G/T | 3.30147e-05 | 0.00406279 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702969 | GTGAGGCCTCTGCCA[G/T]CAAATCTCTCCTCTC | 55135 |
| rs777519727 | in-del | -/T | | | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701851 | ACCTGCACAGGGGCC[-/T]TTTTGTGAGCCGGGG | 55135 |
| rs777564749 | snp | C/T | 1.65463e-05 | 0.00287626 | missense, utr-variant-5-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7689669 | CCCCCAGAGCTGTAC[C/T]ATGAGGGGGAGCAGG | 55135 |
| rs777588420 | snp | C/G/T | 0.000165464 | 0.00909438 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689009 | GAAGAAGCGAACGGG[C/G/T]CAGAGTTGGGGTCTG | 55135 |
| rs777659354 | in-del | -/G | 3.49223e-05 | 0.00417851 | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703524 | CTTCGTGTCTGTTTT[-/G]GGGGGGGCATATGAG | 55135 |
| rs777813887 | snp | A/G | 1.6516e-05 | 0.00287362 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703254 | TCAGCCTGCACCCTA[A/G]CCTGCCTCTCCTGGC | 55135 |
| rs777880143 | snp | C/G | 9.89169e-05 | 0.00703197 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703323 | AGAGTGGGGACGAAG[C/G]AGAGGAGCTGGGCCT | 55135 |
| rs777943410 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7700674 | TCTGCCACAACACTG[C/T]TAGAGGCACGCGCCT | 55135 |
| rs777969109 | snp | C/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691608 | ATATTGGCCAGGATG[C/G]TCTCGTACTCCTGAC | 55135 |
| rs778159976 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700798 | TACTGCTGGTATTCT[C/G]TGATGTCCTCAGCCC | 55135 |
| rs778192810 | snp | A/G | 4.96019e-05 | 0.00497981 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702422 | ATGCCTGTGGCTCCT[A/G]CGGCCGCTCCCTGGG | 55135 |
| rs778225756 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699235 | GACCAGCCTGGCCAA[C/T]GTGGCGAAACCCTGT | 55135 |
| rs778235420 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686333 | CCGGGAAGATGAGAT[A/G/T]TACTCATTCTTGAAA | 55135 |
| rs778282703 | snp | A/C | 1.81338e-05 | 0.00301108 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702546 | CTTCTTCTCAGGAGC[A/C]CGCAAGGTAGGGGTC | 55135 |
| rs778284522 | snp | C/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684967 | TGGCCAATAGGCACA[C/T]GAAAAAATGCTGAAC | 55135 |
| rs778340581 | snp | A/G | 1.86437e-05 | 0.00305311 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702559 | GCCCGCAAGGTAGGG[A/G]TCACACCCTGAGAGC | 55135 |
| rs778763212 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7703093 | GAGCCCGTGTTGAGT[C/T]TTCTGCCCCAGAAGG | 55135 |
| rs778787404 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7693338 | TGGCAAGTTAAATGA[C/T]TATAGTTTCTCTGTT | 55135 |
| rs778850912 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703202 | AGGGAGCAAGTGTCC[C/T]CACTGAAGGCACTGA | 55135 |
| rs779095345 | snp | G/T | 1.68744e-05 | 0.00290463 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689554 | CACTTGAAAAGCATA[G/T]GTCTGGCCAGCTTTC | 55135 |
| rs779179559 | snp | A/G | 1.84633e-05 | 0.00303831 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701889 | GTGGGGGTTCACGCC[A/G]TCCTCTGTACGGCCC | 55135 |
| rs779303064 | snp | C/T | 1.65408e-05 | 0.00287578 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688800 | AAAGGGGGGATCCGC[C/T]CCGGTTGTCCCCAGA | 55135 |
| rs779308330 | snp | A/G | 3.03274e-05 | 0.00389394 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701828 | AGGAGGAGAGGGAAG[A/G]GCACTGCCACCTGCA | 55135 |
| rs779323513 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7700814 | TGATGTCCTCAGCCC[A/T]GCCAGACACCTCCTA | 55135 |
| rs779406985 | snp | C/T | 3.29881e-05 | 0.00406115 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702740 | CCTGTTCCTTGTCTC[C/T]AGGATGCTGAGCTCC | 55135 |
| rs779411378 | snp | C/G | 1.67736e-05 | 0.00289595 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701383 | GTGCTGGGATTACAG[C/G]CATGAGCCACTGTGC | 55135 |
| rs779431250 | snp | A/C | 1.64974e-05 | 0.00287201 | upstream-variant-2KB, missense, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688683 | AACCGTTAGCTCCGG[A/C]CTGCTGTCCTTCAGA | 55135 |
| rs779483078 | snp | C/T | 6.59402e-05 | 0.00574158 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703355 | CCCTTGCTCTCCACG[C/T]GCCACGTCCACCTTG | 55135 |
| rs779492288 | snp | C/T | 8.3603e-05 | 0.00646487 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701400 | ATGAGCCACTGTGCC[C/T]GGCCATTCCTCCCCT | 55135 |
| rs779599073 | snp | A/G | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7684828 | CATTCACGACACATG[A/G]ATCTGATAAAGGACT | 55135 |
| rs779681689 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702759 | ATGCTGAGCTCCTGT[A/G]CTGGGATCTCCGGCA | 55135 |
| rs779696758 | snp | C/G | 1.88902e-05 | 0.00307323 | intron-variant | WRAP53 | GRCh38.p7 | 17:7702567 | GGTAGGGGTCACACC[C/G]TGAGAGCCCAAAGCA | 55135 |
| rs779875361 | snp | C/T | 1.64757e-05 | 0.00287012 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689258 | TCCCAGCTGCCTCGA[C/T]TTCTCAGTGGTTCCT | 55135 |
| rs779914092 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701610 | CTCCTTCCTTGAGGG[C/T]AGCTGAGGCTTTGCA | 55135 |
| rs779983978 | in-del | -/CT | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7694900 | CAGTTCTATCGCAAC[-/CT]CTCTCATTAGGTATT | 55135 |
| rs779998259 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-3-prime, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701691 | ATTCGCTCTGCTTCT[C/T]CCCGGATGGCTCCCA | 55135 |
| rs780213284 | snp | C/T | | | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702404 | GCCCAGCCCAGCCCC[C/T]CTATGCCTGTGGCTC | 55135 |
| rs780223030 | in-del | -/G | 0.000134853 | 0.00821025 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689360 | GAGCTGACCACCCCC[-/G]AGATTTTCACTGTAA | 55135 |
| rs780363627 | snp | A/C | 3.32458e-05 | 0.00407698 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688831 | TCCTGTGGCTGGCTC[A/C]GCTGTGTCCCAGGAG | 55135 |
| rs780367295 | snp | C/T | 0.000267989 | 0.0115725 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701911 | GTACGGCCCCGGGAG[C/T]AGGTGCAGCCCAGTC | 55135 |
| rs780391494 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688260 | GCGTAGGCGCTTCTC[G/T]CCAAGATAGAAGCGT | 55135 |
| rs780433406 | snp | G/T | 1.65097e-05 | 0.00287308 | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703401 | TCTGGTGGTGTGGGG[G/T]GGCGCCAGACTCCAG | 55135 |
| rs780440874 | snp | A/C | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686594 | AACCGGCCTAAAGGA[A/C]ATTTTCTCTCTCTCT | 55135 |
| rs780444705 | snp | A/T | | | missense, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703434 | TCCCTGATGATCACC[A/T]GGGCGAGAAAGGGCA | 55135 |
| rs780547823 | snp | C/G | 0.000115463 | 0.00759725 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7701476 | TGGCCAGCAGCAGCC[C/G]GGAGAACCCGATTCA | 55135 |
| rs780602952 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7697787 | ATACAAATTTATGCT[A/G]TAATGAAATACCATT | 55135 |
| rs780617002 | snp | A/C | 1.6525e-05 | 0.00287441 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688907 | GAGTTTGGTTCCCCT[A/C]GTGAGTTGAGTCCTC | 55135 |
| rs780620391 | snp | C/T | 4.06711e-05 | 0.00450931 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701844 | GCACTGCCACCTGCA[C/T]AGGGGCCTTTTGTGA | 55135 |
| rs780635910 | snp | A/G | 3.30546e-05 | 0.00406524 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7688894 | TCCCCTGGAAACAGA[A/G]TTTGGTTCCCCTAGT | 55135 |
| rs780959583 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7701059 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTGAAG | 55135 |
| rs781041136 | snp | C/T | 1.64754e-05 | 0.00287009 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689271 | GATTTCTCAGTGGTT[C/T]CTGGTCAGAGTTCAG | 55135 |
| rs781045679 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703651 | ACCAGGCAGGAGCCA[A/G]TGGGGCGGCTGAGCT | 55135 |
| rs781128964 | snp | A/G | 3.40808e-05 | 0.00412786 | upstream-variant-2KB, intron-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689372 | CCCGAGATTTTCACT[A/G]TAAAACAGTCCAGTT | 55135 |
| rs781203702 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702795 | GTTACCCACTGTGGT[C/G]CCTGGGTCGAGAGGT | 55135 |
| rs781286877 | in-del | -/AAAC | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691213 | ACTCCATCCCAAAAC[-/AAAC]AAACAAACAAACAAA | 55135 |
| rs781399941 | snp | A/C | 6.61934e-05 | 0.00575259 | intron-variant, upstream-variant-2KB | WRAP53, EFNB3 | GRCh38.p7 | 17:7703221 | TGAAGGCACTGATAG[A/C]CCCTCCCCATCTCTC | 55135 |
| rs781468333 | snp | C/T | 4.94898e-05 | 0.00497418 | synonymous-codon, nc-transcript-variant | WRAP53 | GRCh38.p7 | 17:7702396 | AGCCTTCAGCCCAGC[C/T]CAGCCCCTCTATGCC | 55135 |
| rs781470763 | snp | C/G | 3.36785e-05 | 0.00410343 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TP53, WRAP53 | GRCh38.p7 | 17:7688640 | TCTCCGCTGTGCTTC[C/G]TCTGCAGTATGAAGA | 55135 |
| rs781510017 | snp | A/G | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7689891 | CCCCTTTCTTTAATT[A/G]GGAATCTGTGTTTTT | 55135 |
| rs781521924 | in-del | -/GC | 3.3015e-05 | 0.00406281 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703403 | TGGTGGTGTGGGGGG[-/GC]GCCAGACTCCAGCAT | 55135 |
| rs781581329 | in-del | -/CTTT | 1.66172e-05 | 0.00288242 | intron-variant | WRAP53 | GRCh38.p7 | 17:7701418 | CCATTCCTCCCCTTC[-/CTTT]GACAGCACCGGGGTT | 55135 |
| rs781593838 | snp | A/G | 0.000292355 | 0.0120869 | intron-variant, downstream-variant-500B | WRAP53 | GRCh38.p7 | 17:7701927 | AGGTGCAGCCCAGTC[A/G]GCAGAGGAGCAAACA | 55135 |
| rs781628446 | snp | A/G | 1.65913e-05 | 0.00288017 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | WRAP53, EFNB3 | GRCh38.p7 | 17:7703471 | AACGGAGGGAGGTGT[A/G]GGTGAGCTGATATAA | 55135 |
| rs781665001 | snp | A/G | 3.44359e-05 | 0.00414931 | intron-variant | WRAP53 | GRCh38.p7 | 17:7689707 | TGCAGAAATGGTAAG[A/G]ACTGGGGCTAACTGC | 55135 |
| rs781719919 | snp | A/G/T | 8.27542e-05 | 0.00643207 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | TP53, WRAP53 | GRCh38.p7 | 17:7689000 | CTTTCTGAAGAAGAA[A/G/T]CGAACGGGCCAGAGT | 55135 |
| rs796085393 | in-del | -/TT | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699521 | ATATATATATATATA[-/TT]TATATATATATATAT | 55135 |
| rs796267523 | snp | A/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699482 | TATATATATTTATAT[A/T]TATATATATATATAT | 55135 |
| rs796368936 | in-del | -/AAACAAACAAACAAAC | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691210 | TGAGACTCCATCCCA[-/AAACAAACAAACAAAC]AAACAAACAAACAAA | 55135 |
| rs796407717 | in-del | -/CTC | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7696523 | CAGGATGGTCTCGAT[-/CTC]CTGACCTTGTGATCC | 55135 |
| rs796471061 | in-del | -/GT | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691390 | GAAGTCATGAGAGAG[-/GT]GTTTTTTTTTTTTTT | 55135 |
| rs796607857 | snp | A/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699480 | TATATATATATTTAT[A/T]TATATATATATATAT | 55135 |
| rs796984944 | snp | C/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7691334 | GAAGAGCAGCCACGT[C/T]GTGTTGGTTCTTATG | 55135 |
| rs796999728 | snp | A/T | | | intron-variant | WRAP53 | GRCh38.p7 | 17:7699504 | TATATATATATATTT[A/T]TATATATATATATAT | 55135 |
| rs797011726 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TP53, WRAP53 | GRCh38.p7 | 17:7686304 | CAGACGTACCCATTC[-/T]TTTTTTTTTTCCTCC | 55135 |