SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs76585117 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69808890 | CTATTGCGTATGTAC[A/G]GATCTAGGAGCTTTG | 11060 |
rs76614752 | snp | C/T | 0.123452 | 0.215605 | intron-variant | WWP2 | GRCh38.p7 | 16:69796206 | AGTAAAGGGGCACAA[C/T]GTCTAGAGCTTACTC | 11060 |
rs76655195 | snp | C/T | 0.039522 | 0.134904 | intron-variant | WWP2 | GRCh38.p7 | 16:69877566 | CTTCTCCTTTGCATT[C/T]GCAACTTGGCTAACT | 11060 |
rs76670736 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933595 | TAATAAACATGCATC[A/G]TGCCCTTGTGCAGTG | 11060 |
rs76711306 | snp | A/C | 0.093417 | 0.194889 | intron-variant | WWP2 | GRCh38.p7 | 16:69797092 | TCTAGATGTGTTTTA[A/C]CCTAGCGACCTGGCG | 11060 |
rs76713905 | snp | G/T | 0.244776 | 0.249945 | intron-variant | WWP2 | GRCh38.p7 | 16:69890141 | TTTTTTTTTTTTTTG[G/T]AGAGACAGGGTTTTG | 11060 |
rs76715892 | snp | G/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69897610 | GTTTCTTGACAGCTA[G/T]AAAGAATGGCTGCAG | 11060 |
rs76717380 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69922827 | GTAAAATTGTTGTGA[A/G]GATCAGCTCCCATTG | 11060 |
rs76761193 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69802384 | TTGCAAAACTGAAAT[A/T]CTGTCCCATTAAACC | 11060 |
rs76844572 | snp | C/T | 0.122758 | 0.215196 | intron-variant | WWP2 | GRCh38.p7 | 16:69920265 | CTTAGTAAGTTGCTC[C/T]AGGGTCGACGATCAT | 11060 |
rs76907327 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923790 | CCATGATGTAGAATA[C/T]GTGTGTTTTCTCATT | 11060 |
rs76914349 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69853565 | TAGGCCCTGCAGTGC[A/G]TCAGGGCGGGCATAT | 11060 |
rs76921156 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69802410 | AAACCATGACTCCCC[C/T]ATCCTCCCCTCGCAC | 11060 |
rs76942673 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69890138 | TTTTTTTTTTTTTTT[G/T]TGTAGAGACAGGGTT | 11060 |
rs76982134 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69796528 | CTGCCCAGTAGTACC[A/G]CATATGACTATTCTG | 11060 |
rs76987384 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69861240 | GCAGGTGAACACTTC[C/G]CCTCTGAACTCTCTA | 11060 |
rs77004987 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | WWP2 | GRCh38.p7 | 16:69859220 | GGCTCTGGCAGGACA[A/G]CATTCTTATCTGCAT | 11060 |
rs77013832 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | WWP2 | GRCh38.p7 | 16:69828814 | TATTCCATCCTCTTC[C/T]TCCATGATCTCATCT | 11060 |
rs77016506 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69810429 | AGTTTTTTAACATCT[C/T]TTTTTTTTTTTTTTG | 11060 |
rs77018070 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69918862 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 11060 |
rs77057594 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69784940 | TTTTTTTTTTTTTAA[A/G]GAAAAGAAAGAGTGG | 11060 |
rs77074993 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69818151 | AGTGATTTCTCTTTG[G/T]TATTTTATTTTATTT | 11060 |
rs77100813 | snp | A/T | 0.0748431 | 0.178382 | intron-variant | WWP2 | GRCh38.p7 | 16:69894089 | CATTTTTTTTTTTTT[A/T]AACTGAGATGGAGTC | 11060 |
rs77107835 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69776941 | TTTGTTTAATCTAAA[A/C]CCCTACCTTAGATGG | 11060 |
rs77130573 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69771952 | AAAAGTCTTTTTAGT[C/T]TTTTTTTTTTTTTTT | 11060 |
rs77148491 | snp | A/C | 0.106633 | 0.204807 | intron-variant | WWP2 | GRCh38.p7 | 16:69872148 | TTCTCCATATGACTG[A/C]GCTCTTCTAAAATAC | 11060 |
rs77170278 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69802617 | TTGTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCG | 11060 |
rs77200685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69785967 | TTGTCTTCTTTTTCT[C/T]TTTCCTTTTTTTTTT | 11060 |
rs77211143 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69810444 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCGCT | 11060 |
rs77234177 | snp | G/T | 0.126564 | 0.217402 | intron-variant | WWP2 | GRCh38.p7 | 16:69790973 | ATTACATTATTGATT[G/T]TTTTTGTAGTCTTGA | 11060 |
rs77247008 | snp | A/G | 0.107341 | 0.205301 | intron-variant | WWP2 | GRCh38.p7 | 16:69805990 | TCACTTGAGGCCAGT[A/G]GTTTGAGACCAGACA | 11060 |
rs77253126 | snp | C/G | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69935198 | CCCCTGCCTTCCTGA[C/G]TGTCCCACCCGGCTC | 11060 |
rs77255242 | snp | G/T | 0.0894459 | 0.191631 | intron-variant | WWP2 | GRCh38.p7 | 16:69881447 | GCAATGCAGGATCCT[G/T]GGTTGGATCTTGGAA | 11060 |
rs77271056 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69906090 | TTTCTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 11060 |
rs77319311 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69903767 | GCAAGAATCTGTCTC[A/C]AAAAAAAAAAAAAAG | 11060 |
rs77369989 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849478 | TGTTATTTATTTATT[C/T]ATTTATTCATTCATT | 11060 |
rs77370252 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775232 | TATTTCTTTCCTTGG[A/G]GTATAAGGAGGGCAT | 11060 |
rs77370975 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69904393 | TTTTTTTTTTTTTTT[G/T]AGTTGGGGTCTATTG | 11060 |
rs77376904 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69856943 | AGGTAGTGTTTTTTT[G/T]TAACAGCATTTAACT | 11060 |
rs77414179 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909487 | GTTCAGCTGTCAGGC[A/G]TGTGCCACACACATC | 11060 |
rs77458741 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69848135 | ATAGGGATTAACATA[A/G]GGGATCTTAGTTAAG | 11060 |
rs77505031 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69872219 | ACAATAAAAAGAAAT[A/G]TCTTTTTTTTTTTTT | 11060 |
rs77517847 | snp | A/C/G | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69796214 | GGCACAATGTCTAGA[A/C/G]CTTACTCTCAGAGTT | 11060 |
rs77530424 | snp | C/T | 0.084364 | 0.187256 | intron-variant | WWP2 | GRCh38.p7 | 16:69792133 | TGGGGTGTGACTGCG[C/T]GGTTTCCAGTTCCCT | 11060 |
rs77530869 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805792 | TTCTTTTTTTTTTTT[-/TTT]AGAGATGGTATCTCA | 11060 |
rs77533998 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923429 | GCTGAGATTTTTTTT[A/T]AAAGGCAAGGATTCA | 11060 |
rs77556105 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69795313 | ACAGAGACATAGATG[A/G]CATTTATCTATAACC | 11060 |
rs77560846 | snp | C/T | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69872451 | TTGATCTCCTGACCT[C/T]GTGATCGCCCGTCTT | 11060 |
rs77620507 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826228 | ACTGAGATCACACCA[C/T]TGCACTCCAGCCTGG | 11060 |
rs77623554 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69896345 | GCTGGTCTTGAACTC[C/T]TGGAGGCTCAAGCGA | 11060 |
rs77624839 | in-del | -/AAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899725 | AGTGAGACTCCGTCT[-/AAA]CAAAAAAAAAAAAAA | 11060 |
rs77641108 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69877656 | ACTTAATAATATCTA[G/T]TATTTGATTTAAAGT | 11060 |
rs77642842 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69834213 | ACCTCCTGCCCTCAT[A/C]TGCTCCTCTCTTCCC | 11060 |
rs77644035 | snp | A/G | 0.151668 | 0.229849 | intron-variant | WWP2 | GRCh38.p7 | 16:69859935 | ACGACATACTTGACG[A/G]CATACTCAAGGGTGT | 11060 |
rs77702396 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785983 | TTTCCTTTTTTTTTT[C/T]CTTGCATTATACTTT | 11060 |
rs77757767 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | WWP2 | GRCh38.p7 | 16:69892502 | CCATGATCTGTCACT[C/T]GAGTGACTGTTCTTA | 11060 |
rs77770514 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69800179 | CTCCTCTGGTCTTTT[C/T]TTTTCGGCTGGGCAC | 11060 |
rs77771398 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940972 | GGGACACAGGGGTCC[A/G]GCTGTGGAGCTCCCC | 11060 |
rs77786756 | snp | A/G/T | 0.00519481 | 0.0506999 | synonymous-codon, missense | WWP2 | GRCh38.p7 | 16:69930184 | GAAATACACCAGCGA[A/G/T]GGGGTGCGATACTTT | 11060 |
rs77787174 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910202 | TATCCATATTTCACT[A/G]TGTATTTCTAAAACA | 11060 |
rs77787935 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69887414 | ACACTTTTTTTTTTT[G/T]AGACACAATTTTGCT | 11060 |
rs77790472 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69846723 | AGACTCTGTCTCAAG[A/G]AAAAAAAAAAAAGAA | 11060 |
rs77828470 | snp | A/G | 0.0448719 | 0.142907 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933517 | TACGTTATGTTGCCC[A/G]CCCAGGTAGAGTGGA | 11060 |
rs77829805 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69887952 | CATTGTAGATACCAT[C/G]TTAGCCTATTAAGTG | 11060 |
rs77834778 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861847 | CTGGAAACTGGCCCA[G/T]CTCCACTGAATTTTT | 11060 |
rs77870048 | snp | C/T | 0.062967 | 0.165888 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931118 | CATTTTCTGAGAAAT[C/T]GCATGAACCCCTGAA | 11060 |
rs77871607 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69891046 | TGCTCTTCTCTAAGA[C/T]GGCTAGGAGGGCTCT | 11060 |
rs77882012 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69886105 | TTGGTTGATTGATTG[A/G]TGGGTCTCACCCTGT | 11060 |
rs77899313 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69808285 | TCTTTTTTTTTTTTA[A/T]TAGAGATGGGATCTC | 11060 |
rs77904244 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69784941 | TTTTTTTTTTTTAAA[G/T]AAAAGAAAGAGTGGT | 11060 |
rs77918990 | snp | C/T | 0.0205511 | 0.0992634 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941962 | GGTCAGCTGCCTCAC[C/T]GTACCCTTTCGGCAC | 11060 |
rs77951731 | in-del | -/AGC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914432 | CATCCTTCTTCTCAG[-/AGC]CTGTAGAGCAGGACC | 11060 |
rs77990310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908965 | CAGTGACGTTTATTC[C/T]GGGTCACTTGATTGC | 11060 |
rs77993367 | in-del | -/A | 0.201727 | 0.245295 | intron-variant | WWP2 | GRCh38.p7 | 16:69908465 | ATGCTGAATTTTTTT[-/A]AAAAAATCCATGGAA | 11060 |
rs78014367 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69856942 | TAGGTAGTGTTTTTT[G/T]GTAACAGCATTTAAC | 11060 |
rs78047418 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | WWP2 | GRCh38.p7 | 16:69886847 | TCCCTGTAAGAAACG[G/T]TCACGAAGAATCTGG | 11060 |
rs78054921 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868686 | ACACACACACACACA[C/G]ACACACAGACATACA | 11060 |
rs78100281 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | WWP2 | GRCh38.p7 | 16:69763944 | AAAACAGGCTCGAGA[C/G]AAAGGCTTGGATTGG | 11060 |
rs78101416 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69877105 | ATGAACTTCTCTTTA[C/T]CTATGAATGTCCAAG | 11060 |
rs78115637 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | WWP2 | GRCh38.p7 | 16:69865983 | GGGTTGATTTTTGTT[C/T]GACACTGAGGAAAGA | 11060 |
rs78154731 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69896532 | GGAGTGATGTGTTAC[A/T]TGAGTGGGAAAATGA | 11060 |
rs78161421 | snp | A/T | 0.121717 | 0.214577 | intron-variant | WWP2 | GRCh38.p7 | 16:69804757 | TTTTATGGAGTCCTG[A/T]CATATGTAAAGTTAA | 11060 |
rs78222233 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69834873 | ATTTTCTTTTTTTTT[A/T]AAGGAAAAAAAGAAA | 11060 |
rs78232334 | snp | A/T | 0.0711525 | 0.174681 | intron-variant | WWP2 | GRCh38.p7 | 16:69881257 | ACGCCCACTGTTTTT[A/T]CTTCGTGGTGTTCTG | 11060 |
rs78235002 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | WWP2 | GRCh38.p7 | 16:69869323 | ATGAGGGACTCCAGA[A/G]TTTGCTACGTTTCTC | 11060 |
rs78252493 | snp | A/G | 0.151334 | 0.229706 | intron-variant | WWP2 | GRCh38.p7 | 16:69860246 | GATTGGAAAGAATAT[A/G]CAAAGTACTGGAGGT | 11060 |
rs78261915 | snp | A/C | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69798282 | GCGAACAATTGCAAG[A/C]AGTCTATTCGACAAT | 11060 |
rs78341767 | snp | A/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69770972 | ATCCTGTCTCTATTA[A/T]AAAAAAAAAAAAAAG | 11060 |
rs78347773 | snp | A/G | 0.152334 | 0.230133 | intron-variant | WWP2 | GRCh38.p7 | 16:69899055 | GCTTCTCAATTATAC[A/G]CATTGCAAATATTTG | 11060 |
rs78354043 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839989 | CTTTTTTCCATGCCA[C/T]GAGGCAAAATGTGAA | 11060 |
rs78371550 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69896129 | CTACTGCACTTTCTT[C/T]CCTTTTTTTGGAGAC | 11060 |
rs78419136 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | WWP2 | GRCh38.p7 | 16:69779864 | CATTATTCAAGATAC[A/G]ATCTTTTGCTTCCCC | 11060 |
rs78426175 | snp | C/T | 0.00148155 | 0.0271769 | missense | WWP2 | GRCh38.p7 | 16:69888129 | CCTTGAGTGTGACCC[C/T]GAATCCCAACACGAC | 11060 |
rs78432537 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839928 | AGTGCAGCTTCCCCT[C/T]CAGCCTGATACAACA | 11060 |
rs78460209 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847880 | TTTCAACATGAATTT[C/T]GGTGGGGACAAACTG | 11060 |
rs78468185 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69872220 | CAATAAAAAGAAATG[G/T]CTTTTTTTTTTTTTG | 11060 |
rs78470772 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69899801 | ATTTAATTGGCAGTG[G/T]TTTTTTTCTTAGTGT | 11060 |
rs78567017 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69816303 | AAAATAATTACTTAG[C/T]CCAGTGCAGTGGCTC | 11060 |
rs78586868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69829876 | AGCAAATGTTACTTG[A/G]ACCTCCTGGGTTCAA | 11060 |
rs78626384 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69767061 | TTTTTAATCTTTTTG[A/T]AAACCACAAGCTAAT | 11060 |
rs78677286 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69825642 | TTTGGTTTTTTTTTT[G/T]GGATACAGGGTTTTG | 11060 |
rs78683583 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69809936 | GCCCCATGGGCTTGC[C/T]CCTTGCTCTTGGTGT | 11060 |
rs78727023 | snp | C/T | 0.260227 | 0.249791 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931377 | GCTGTCTCTAGGAAG[C/T]TAGTTTTCATTCCTA | 11060 |
rs78732099 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69829863 | ATAGTGGGCACCCAG[A/C]AAATGTTACTTGAAC | 11060 |
rs78743502 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69810442 | CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTTTCG | 11060 |
rs78792498 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69871184 | AGCTACTGGGGAGGC[G/T]GAGGTGGAAGGATCA | 11060 |
rs78801630 | snp | A/T | 0.0014084 | 0.0264994 | intron-variant | WWP2 | GRCh38.p7 | 16:69842142 | CCCCCCTTGGTGAGG[A/T]CAAAGAGCTAAGAAG | 11060 |
rs78818137 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69899729 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 11060 |
rs78819380 | snp | A/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69918822 | TAAAGAGTAACATTT[A/T]AATTTTCTTTTTCCT | 11060 |
rs78824052 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864957 | TAATGATATCTCATT[A/G]TAGTTTTAATTTGCA | 11060 |
rs78843422 | snp | A/C | | | missense | WWP2 | GRCh38.p7 | 16:69934047 | CCGGAAAGAACAATT[A/C]CTGCCTGCAGATCAA | 11060 |
rs78891517 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69836347 | TTTTCAGGAGTTCAG[C/G]ACAGTTATTGTATGG | 11060 |
rs78905986 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69823138 | TGTGTCTCAAAAAAG[A/G]AAAAAGTAAAAACAA | 11060 |
rs78914115 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69825644 | TGGTTTTTTTTTTTG[G/T]ATACAGGGTTTTGTT | 11060 |
rs78920163 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69771976 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTT | 11060 |
rs78944503 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | WWP2 | GRCh38.p7 | 16:69794943 | GTCTGGGGACTGGGC[A/G]GTAGCTCATGTTTGT | 11060 |
rs78985537 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785645 | TTTTTTTTTTTTTTC[G/T]AGACAGAGTCTTGCT | 11060 |
rs79005887 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WWP2 | GRCh38.p7 | 16:69894692 | TGGGCAATGGGAAGC[A/G]AGGCTGCTTTGGTCT | 11060 |
rs79015278 | in-del | -/G | 0.319616 | 0.240112 | intron-variant | WWP2 | GRCh38.p7 | 16:69852973 | AGTTTGCCAGTCCCT[-/G]GCTGTAGGAGATGGT | 11060 |
rs79025825 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69786945 | TTGAGTTAAACTCCT[A/C]TGTCTTCTTATCAGA | 11060 |
rs79042252 | snp | A/G | 0.108048 | 0.20579 | intron-variant | WWP2 | GRCh38.p7 | 16:69771063 | TCCTCTCAGTAAGTA[A/G]CTTGCTCTGGATCAC | 11060 |
rs79067135 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | WWP2 | GRCh38.p7 | 16:69860660 | CATATTCTTTTTGGA[A/G]CCTGCCTCCGTCCTG | 11060 |
rs79114689 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69850794 | CAGCCTGCCATCTGC[C/T]TTTTTGTTGGTGTTC | 11060 |
rs79146280 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WWP2 | GRCh38.p7 | 16:69879581 | GGCTGAATAATATTC[C/T]GTTGTATATACATAC | 11060 |
rs79173709 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69935460 | GCTGCCTTTGCCACC[A/C]ACCCTGAGCGCCAGT | 11060 |
rs79232673 | snp | A/G | 0.0191209 | 0.0958897 | intron-variant | WWP2 | GRCh38.p7 | 16:69936014 | CCCCCTTGCCCCACC[A/G]CGCTGATAGGAGGGA | 11060 |
rs79237496 | in-del | -/T | 0.315516 | 0.241263 | intron-variant | WWP2 | GRCh38.p7 | 16:69841697 | TTTGCATGGTTAGGG[-/T]TTTGTTCTCTATCTC | 11060 |
rs79269632 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69872235 | TCTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACC | 11060 |
rs79318189 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69794529 | GGGAGACCCGGTCTC[A/C]AAAAAAAAAAGAAAC | 11060 |
rs79319032 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69816421 | ACCCACCGCTCTATT[A/T]AAAAAAAATCTATAT | 11060 |
rs79330949 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69870297 | CCTTTATTTATTTAT[C/T]CTTTTTTTTTTTTTT | 11060 |
rs79352169 | in-del | -/TTGT | 0.0752113 | 0.178743 | intron-variant | WWP2 | GRCh38.p7 | 16:69827437 | TAATTTTCCATGTTG[-/TTGT]TTGTATACGCTTTAT | 11060 |
rs79354418 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815625 | ACCCCCGTCTCTACT[A/G]AAAATACACAAATTA | 11060 |
rs79358118 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69886269 | AATTATTTGTAGAGA[C/T]GAGTCCTCGCTAGGT | 11060 |
rs79386368 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761572 | AGCGAGGCTCCATCT[A/C]AAAAAAAAAAAAAAA | 11060 |
rs79416883 | snp | G/T | 0.093417 | 0.194889 | intron-variant | WWP2 | GRCh38.p7 | 16:69771073 | AAGTAACTTGCTCTG[G/T]ATCACTCAAAGGCAA | 11060 |
rs79451708 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69811574 | GTATTGTAGTGAGAC[A/C]CAGTCTCTACAAAAA | 11060 |
rs79472988 | snp | C/T | 0.081446 | 0.184634 | intron-variant | WWP2 | GRCh38.p7 | 16:69862948 | GCCAGGCTGGGTTTG[C/T]ACTCTTGGGCTCAAG | 11060 |
rs79485153 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926040 | GGTGGTGACTCTGGA[A/G]ACGCATCGCTGCTAG | 11060 |
rs79525236 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785229 | TGTGTGAGACTGTCT[A/C]AAAAAAAAAAAAAAG | 11060 |
rs79538546 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69824106 | TTTGGGCCTCTGCTC[C/T]GCACCAGTCATTCGG | 11060 |
rs79552566 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69903786 | AAAAAAAAAAAGAAA[A/G]AAAGAAAAATGTGTT | 11060 |
rs79569203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925209 | AAAACTCACTTGGGC[C/T]CTCCGTGCGCAGGGT | 11060 |
rs79590287 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69863654 | TCAAAAACAAACAAA[C/G]AAACAAACAAACAAA | 11060 |
rs79600219 | snp | A/G | 0.121717 | 0.214577 | intron-variant | WWP2 | GRCh38.p7 | 16:69804756 | ATTTTATGGAGTCCT[A/G]TCATATGTAAAGTTA | 11060 |
rs79603167 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867155 | CTTTTTTTTTTTTTT[-/TTT]AAACCAAACAAACAA | 11060 |
rs79622126 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | WWP2 | GRCh38.p7 | 16:69934691 | AGTGTAGAACAAAAC[A/G]TAAAGTCTGTGGCCC | 11060 |
rs79685426 | snp | A/T | 0.20111 | 0.245173 | intron-variant | WWP2 | GRCh38.p7 | 16:69764293 | TAACCTTGACCTGCC[A/T]GGGCTCGGGTGATCC | 11060 |
rs79689829 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | WWP2 | GRCh38.p7 | 16:69819608 | AGATGGGATCTCACT[A/G]TGTTGACTAGGCTGG | 11060 |
rs79696706 | snp | G/T | 0.323434 | 0.238972 | intron-variant | WWP2 | GRCh38.p7 | 16:69849911 | ATACATTTATTTATT[G/T]CATAGATATTTATTT | 11060 |
rs79710401 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69918391 | ATCAGGGATTGGCAA[A/T]TAATAGTCCATGGGC | 11060 |
rs79720196 | snp | C/T | 0.031825 | 0.122064 | intron-variant | WWP2 | GRCh38.p7 | 16:69867437 | CTCAGAAAAGGATGA[C/T]TGAGTACATTTCAGC | 11060 |
rs79732641 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815936 | CTAATTTTTAAATTT[A/C]TTGTAGAGTCAGGGT | 11060 |
rs79740125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881234 | CATCAAAGCTGTCTT[C/T]GCTCCCCACGCCCAC | 11060 |
rs79762324 | snp | A/C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939720 | TGAAGGCCTGACTGG[A/C/G]AGCCCCTGAGCCCTA | 11060 |
rs79765820 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69825426 | GAGATTCCATCTCCA[A/C]AAAAAAAAAACCCCA | 11060 |
rs79810797 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | WWP2 | GRCh38.p7 | 16:69830893 | TCAGGGAACTGGGGA[A/G]TGGAAAGGAGACTGT | 11060 |
rs79815530 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69779453 | ACATGGTGATGTTTT[A/G]TCTACCCTGTTTCTC | 11060 |
rs79839225 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69929983 | CAGAACTGTTCTCAC[A/G]ACTTGGGTCATGCTT | 11060 |
rs79918326 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69815803 | AAAAAAAAAAAAAAA[A/G]GGCAATGGAATCATA | 11060 |
rs79934309 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69904688 | AGTGTGCATTTTCAT[C/T]TGGCCACTTTTGCCA | 11060 |
rs79943852 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932475 | GAGGACTCCTGGGAG[C/G]GGCGAGAGCTCAGTA | 11060 |
rs79980498 | in-del | -/T | 0.322721 | 0.23919 | intron-variant | WWP2 | GRCh38.p7 | 16:69847092 | TTATTTATTTATTTA[-/T]TTTTAAATTTGAGAT | 11060 |
rs79992861 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69887413 | AACACTTTTTTTTTT[G/T]GAGACACAATTTTGC | 11060 |
rs79993961 | snp | C/T | 0.118933 | 0.212888 | intron-variant | WWP2 | GRCh38.p7 | 16:69928955 | CTGATCAGAGAGGTG[C/T]GAGGGAAATGCAGCC | 11060 |
rs80009070 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69810441 | TCTTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC | 11060 |
rs80118156 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69855670 | AATGTAACCATGAGG[A/C]TATCTGGGGAAAGAG | 11060 |
rs80121670 | snp | C/G | 0.0919752 | 0.193722 | intron-variant | WWP2 | GRCh38.p7 | 16:69796033 | TTCTTTTTTTTTTTG[C/G]GATGATGGGCATCGA | 11060 |
rs80126515 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69906079 | CTTTTCTTTTCTTTC[C/T]TTTTTTTTTTTGAGA | 11060 |
rs80150886 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69816313 | CTTAGCCCAGTGCAG[C/T]GGCTCACGCTTGTAA | 11060 |
rs80204522 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69894676 | ATAGTGGTTCAGGCC[A/G]TGGGCAATGGGAAGC | 11060 |
rs80215330 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | WWP2 | GRCh38.p7 | 16:69823242 | AGTATAAAGAAAAGT[A/G]CTAATGAGATATTTT | 11060 |
rs80233577 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69895845 | TTTGGGCTGTGGACC[A/G]TTCTTTGAGTAGCAT | 11060 |
rs80278767 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847878 | AATTTCAACATGAAT[A/T]TTGGTGGGGACAAAC | 11060 |
rs80292286 | snp | C/T | 0.00898908 | 0.0664359 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842088 | GAACCGGCACCAGCC[C/T]CCCAGCACAAACTGC | 11060 |
rs111227164 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69795045 | TCGAGATCAGCCTGG[C/T]CAATGGGGTGAAATC | 11060 |
rs111279410 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69897121 | GTTTGTGTGTTTTGT[C/T]TTTGAGACAGAATCT | 11060 |
rs111317504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69803471 | CATAGTTTCACCATT[C/T]TTCTCAACATGTCGT | 11060 |
rs111335581 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | WWP2 | GRCh38.p7 | 16:69800626 | CTGGAGTGTAGTGGT[A/G]CAATCTCGGCTCACT | 11060 |
rs111356004 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69901641 | TCTAATGGAGAGAGT[A/G]GATTTTGATTGAGTT | 11060 |
rs111358678 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69857882 | GTTGCCTAGTCTGGT[C/G]TTGGATCCTCTTTCC | 11060 |
rs111366342 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933159 | CCACAGGGTAGAACC[A/G]CGGACAGGATACCGG | 11060 |
rs111375749 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69841894 | TGGCTGCAGCTTGCC[A/G]GATGTCCATATCCCG | 11060 |
rs111383464 | in-del | -/A | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69789576 | AGTGCTCCTCCTTGG[-/A]AAAAAACCAGTATTG | 11060 |
rs111390959 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761440 | TAGCCAGGCGTGGTG[A/G]TGCACGCCTGTAATC | 11060 |
rs111423074 | snp | C/T | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69798316 | AGAATAGTTAACATA[C/T]ACCTATTATGGGCTT | 11060 |
rs111437075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836672 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 11060 |
rs111456866 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69817862 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 11060 |
rs111467709 | snp | G/T | 0.00056425 | 0.0167871 | intron-variant | WWP2 | GRCh38.p7 | 16:69929540 | CAGGGGTAAGGACTT[G/T]GGCTGAGAGGGGGGC | 11060 |
rs111513465 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69879349 | TCATCCCAAACGGAT[G/T]CTCTGTATCCATTAA | 11060 |
rs111553293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862542 | AGGCATGAGCCACCA[C/T]GCCTGGCCAGTAATC | 11060 |
rs111563078 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69876705 | ACTTGAAAGGCAAGA[C/T]GACTCCTTGATCCAT | 11060 |
rs111563827 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932610 | GTTGACCCTGGGATC[C/T]CCTCCTCTTAAGGCA | 11060 |
rs111597259 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69777190 | CACATATGTGTATAT[A/G]CAATATACATATGGA | 11060 |
rs111603054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817215 | CGCATCAGTGAAACT[A/G]GGTCAGTTTTAATGG | 11060 |
rs111609401 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69822478 | AGATGCGATGGAGCA[A/T]AGTACAGGATGATCT | 11060 |
rs111610943 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776596 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 11060 |
rs111612968 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69887562 | AGGTGTGCGCCACCA[C/T]GCCCAGCTAAATTTT | 11060 |
rs111616735 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69887299 | CTTTAGTGTGTATGA[A/G]CTTTTTGAAAGAAGG | 11060 |
rs111618369 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | WWP2 | GRCh38.p7 | 16:69795210 | CACTGCACTCCAGCC[G/T]GTCTACAACTTACTT | 11060 |
rs111625113 | in-del | -/A | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69883153 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 11060 |
rs111631471 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69830573 | GAGACTGCAAGACCA[A/G]GCCAGAGTTCTCATT | 11060 |
rs111632240 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69858694 | TTAAGGTTAGTATTG[C/G]AATCAGAGAAGAATT | 11060 |
rs111650027 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69766029 | GTCTAGCCTAGGCCT[C/G]TCTCGAGACTTCTAG | 11060 |
rs111650065 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69820040 | GATGGGGTTCGAGAC[C/T]AGCCTGGGCAACATA | 11060 |
rs111653058 | snp | C/T | 0.48 | 0.0979796 | intron-variant | WWP2 | GRCh38.p7 | 16:69798425 | AAGGCAATTTACCAA[C/T]GATAAATTGGTGATG | 11060 |
rs111657053 | snp | C/T | 0.20111 | 0.245173 | intron-variant | WWP2 | GRCh38.p7 | 16:69786381 | GAACTCCCAACCCTG[C/T]AATCCACCCGCCTCC | 11060 |
rs111662567 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69852545 | TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGCT | 11060 |
rs111729300 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69927921 | CCTGCCTCAGCCTCC[A/C]AAAGTGCTGGGATTA | 11060 |
rs111744596 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850402 | AAAAAAAAAAAAAAA[A/T]TGATGAAAAGTCAGG | 11060 |
rs111751335 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69925744 | CTAAGAAAAGATGTC[C/T]CTGAGCAGCTGGGGG | 11060 |
rs111762394 | snp | A/G | 0.031825 | 0.122064 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941912 | CTGGGCTGGGCAGCT[A/G]AGTCCTGGCCCAGGG | 11060 |
rs111763199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69803949 | GAATGGCAGAGCAGC[C/T]TCCACCCTACTTTTT | 11060 |
rs111778979 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69894193 | TAATACTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 11060 |
rs111786439 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69798874 | AGCAAGATGGGGAAA[A/G]AGAGAGGGTGCTCCG | 11060 |
rs111820033 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69862953 | GCTGGGTTTGCACTC[C/T]TGGGCTCAAGCAGTC | 11060 |
rs111820456 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870531 | GTCTCAAACTCCTGG[A/G]CTCAAGTGATCCTCC | 11060 |
rs111828291 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | WWP2 | GRCh38.p7 | 16:69809289 | TTCCAGCCATGTTTC[A/G]TAAAGTCTTCTATTT | 11060 |
rs111829274 | in-del | -/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69906078 | CTTTTCTTTTCTTTC[-/T]TTTTTTTTTTTTGAG | 11060 |
rs111836396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831604 | TCATCCTTGCTGCAC[A/G]TACAAACTCTTCTCA | 11060 |
rs111836545 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69834190 | GGCCTGACTGGGAGG[C/T]TCTGGCTACCTCCTG | 11060 |
rs111837947 | in-del | -/GT | 0.464416 | 0.128553 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923322 | GTGTTGGGGGGGTGG[-/GT]GGGGGGTGCGTTCTG | 11060 |
rs111843629 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69828382 | TTTTATTAATTTTCT[C/T]TGAGACATAGTTTCG | 11060 |
rs111845105 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | WWP2 | GRCh38.p7 | 16:69775392 | AAATGCCAAGGTGTC[A/G]TGTTTTGGGGTAAGG | 11060 |
rs111848099 | in-del | -/G | 0.138886 | 0.22395 | intron-variant | WWP2 | GRCh38.p7 | 16:69778621 | TACTTTGATGGGGAT[-/G]GGGATCTGTTCCTTT | 11060 |
rs111922813 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69798614 | AAAAAGAGCCGGAAC[A/G]TCTGCCACAGGGGGG | 11060 |
rs111926603 | snp | C/T | | | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931546 | TGAAGATCAGCGTTT[C/T]CAGGCAGACGCTTTT | 11060 |
rs111941799 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WWP2 | GRCh38.p7 | 16:69825998 | GCAGCCAGGCGCGGT[A/G]GCTCATGCCTGTAAT | 11060 |
rs111978592 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69778090 | ATATATATATATATA[C/T]ACACACACACACACA | 11060 |
rs111988145 | in-del | -/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69880750 | TTGCTTGTGTTTCAC[-/G]GGGTGAAAGACACCA | 11060 |
rs111988573 | snp | A/G | 0.0260105 | 0.111035 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761785 | TGCCCCACAAAGGCT[A/G]AGATGTTTGTGGTCC | 11060 |
rs111997152 | in-del | -/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785628 | ATGATGCTGCACATC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs112000001 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913015 | TTTTTTTTTTTTTTT[A/T]TTTTTTTTTTTTTTT | 11060 |
rs112003540 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69881304 | TGCTACTTGCTGACT[A/G]CACAACACCTCTCTG | 11060 |
rs112010616 | snp | A/C | 0.0142736 | 0.0832652 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940326 | AGTTCGGCGAGGAGA[A/C]TGGCCACTGGGGGTG | 11060 |
rs112010752 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69897181 | GGTCTCAGCTCACTG[A/C]AGCCTTGACCTCCCA | 11060 |
rs112018689 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69853746 | GGAGGTGTAATTAAG[C/G]AGGACTGCATGGCTG | 11060 |
rs112031059 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69887898 | TTCAAAGTCATGTTT[C/T]GTAAAACTTTTTGCT | 11060 |
rs112038213 | snp | C/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69802090 | ACCCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 11060 |
rs112047325 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69935274 | TGGCCGGCCCTTCCC[A/G]TCGTCGAGGAGTTCT | 11060 |
rs112059775 | snp | C/G | 0.106633 | 0.204807 | intron-variant | WWP2 | GRCh38.p7 | 16:69876389 | TTTGTTTTTGAGATG[C/G]AGTCTCACTCTGTTG | 11060 |
rs112071187 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69811379 | TGGGAGGCTAAGGCA[A/G]GAGGTTTGCTTGAGC | 11060 |
rs112078280 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69906877 | AGAGCAAGACTCTGT[C/T]TTTAAAAAAATAAAA | 11060 |
rs112089659 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69794985 | TTTGGAAAGCTCTGG[C/T]GGGTAGATCGCTTGA | 11060 |
rs112116181 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69827358 | AAGATCGCGCCACTG[A/C]ACTCCAGCCTGGGCG | 11060 |
rs112117896 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69877954 | CTGGGATTATAGGCG[C/G]GTGCCACCGTGCCCA | 11060 |
rs112139413 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69846692 | CGCCACTGCACTCCA[A/G]CTGAGTGATGGAGTG | 11060 |
rs112152183 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69787412 | TGGGAAACATAGGGA[A/T]GCCCTGTCTCTACAG | 11060 |
rs112156565 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69894863 | ACACACACAGAGGCA[A/C]ATTATTTTGCCCTGG | 11060 |
rs112163450 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69803866 | TGAGCTGAGATTGTG[C/T]CACTGCAGTCCAGCC | 11060 |
rs112170887 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69763213 | ACCTAGACTGCTTTA[C/T]GACTTTTCTCTTTCT | 11060 |
rs112206734 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910602 | TTTTAGTAGAGACAG[A/G]GTTTCACCATTTTGG | 11060 |
rs112217881 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69901811 | TTGCTGTTAGCCAGG[C/T]GTGGTGGCGAGTCCC | 11060 |
rs112229757 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WWP2 | GRCh38.p7 | 16:69883953 | CGTGGTCAGCTATTT[C/T]GTAATAATTATTTTT | 11060 |
rs112231122 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69870256 | AGTTCAGTGAATATT[A/G]TATACTTCTGTAGCC | 11060 |
rs112233666 | in-del | -/T | 0.296619 | 0.245615 | intron-variant | WWP2 | GRCh38.p7 | 16:69913200 | TGTAATTTTTTTTTT[-/T]AAAGTAGAGATGGGG | 11060 |
rs112259070 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69786536 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGCTCAA | 11060 |
rs112275322 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69803549 | CATTCATTGGTTGTT[C/T]TATCTCTGAGGCCCC | 11060 |
rs112285463 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761590 | AAAAAAAAAAAAAAA[A/T]ATCATCTATCTATCC | 11060 |
rs112287968 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835442 | GTTCTCTGAAGTTTA[A/G]TTTTTTAAATAACCT | 11060 |
rs112313652 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69855127 | GCTGGGATTACAGGC[A/G]TGAGCCGCTGAGCCC | 11060 |
rs112324488 | snp | A/T | 0.147656 | 0.228091 | intron-variant | WWP2 | GRCh38.p7 | 16:69813621 | GTGTGTGCTGGCTAA[A/T]TTTTTTATTTTTATT | 11060 |
rs112328328 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923090 | AGACAGGGTTTCCCC[A/G]TGTTGGCCAGGCTGG | 11060 |
rs112369211 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69805287 | GCGATTTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs112396053 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69861415 | TGAGAAGGTTGCTCT[G/T]TACTCTAGGGTGCGC | 11060 |
rs112422074 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69935751 | TCTGTCAGGGAAGGA[A/G]GGCGGGTAGCGGTAG | 11060 |
rs112423897 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69914481 | AATGATTTCCTGCCG[G/T]GCACAGTGGCTCAAA | 11060 |
rs112425716 | snp | G/T | 0.00401711 | 0.0446365 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69798719 | GCATAATCGTCAACC[G/T]CGAATTAACTCCTAC | 11060 |
rs112472736 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | WWP2 | GRCh38.p7 | 16:69887310 | ATGAGCTTTTTGAAA[C/G]AAGGTGCTAGTCATG | 11060 |
rs112484554 | in-del | -/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69888709 | GTTTTCTTGCCATCC[-/T]TTTTTTTTTTTTAGA | 11060 |
rs112498382 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69873936 | ATTTATTTTTAGGTA[C/T]CATTACTTGTTGTCC | 11060 |
rs112506420 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69904947 | ACATAGCAAACTACA[A/G]CCTAACTTAGTACGT | 11060 |
rs112514360 | in-del | -/CTCA | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69832570 | TTTTTGAGACAGAGT[-/CTCA]CTCCATCACTCAGTC | 11060 |
rs112519971 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69815283 | GCTGGGATTACGGGC[A/G]TGAGCCACCTCACCC | 11060 |
rs112569189 | snp | C/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69794075 | GGCGTGCGCCACCAC[C/G]CCCGGCTAAGTTTTG | 11060 |
rs112569706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69830138 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 11060 |
rs112571713 | in-del | -/T | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773964 | GGATCACTTGGGGAA[-/T]TTTTAAATAACACAG | 11060 |
rs112620231 | snp | A/C/G | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69930867 | ACAGAGCAAGACCCC[A/C/G]TCTCTAGAAAACGAA | 11060 |
rs112654508 | in-del | -/TTAAG | 0.139225 | 0.224118 | intron-variant | WWP2 | GRCh38.p7 | 16:69780390 | CCCATTGATGGGTAT[-/TTAAG]TTGTTTATAATTTTT | 11060 |
rs112657942 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69891530 | CTTTCATTAGACAGA[A/T]TATCTGTTACTATTT | 11060 |
rs112682906 | snp | C/G | 0.031825 | 0.122064 | intron-variant | WWP2 | GRCh38.p7 | 16:69789469 | TCATGACCTCATGAT[C/G]TCCCCGCCTCGGCCT | 11060 |
rs112723383 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69847977 | TCCTCCTAGCACCTC[A/G]CGACTTCCTCTGGCT | 11060 |
rs112724219 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762244 | GGCCAGAGGTGCCCA[C/G]GCCAGGCCTAGGTGG | 11060 |
rs112757461 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69900608 | GATCACTGCATCCTC[C/T]GCCTCCTGGACTCAA | 11060 |
rs112773205 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933091 | CTGTGTGTGTCTCTC[C/T]CTGTGTCCTGCCAGT | 11060 |
rs112790916 | snp | G/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69936506 | CGTGGAGATCTAGTG[G/T]GTTGCAGAGAAAGAT | 11060 |
rs112804217 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820436 | TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGC | 11060 |
rs112810285 | snp | A/C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69896811 | CTGCCCAGTTTCCTA[A/C/T]CTGGATGATTTCATG | 11060 |
rs112819988 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69819273 | AGCCAGAATAATTCA[A/G]ACCAGAAGTCAAATT | 11060 |
rs112847203 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828902 | TCACTTCTGAGCTCT[C/G]TTCCCACGTATCTGA | 11060 |
rs112851524 | in-del | -/CACA | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69883401 | TTCTAAGAATGTGCG[-/CACA]CACACACACACACAC | 11060 |
rs112859983 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932990 | TGGCGTTGCCTTCTG[C/T]GCTGGCCCCGTGGAT | 11060 |
rs112865773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909339 | GTATTCTGCTCCAAG[A/G]AAGAATCACCTCCCA | 11060 |
rs112870497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907032 | CATGTTAAATGATTA[C/T]GAAATAGATAACACT | 11060 |
rs112918978 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69879936 | GCATTTAAAAAATGT[G/T]TATAATTTCGGTTTT | 11060 |
rs112927250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785140 | CATGAGGCTGAGGCA[C/T]GAGAATCACTTCAAC | 11060 |
rs112927275 | snp | C/T | 0.449218 | 0.151037 | intron-variant | WWP2 | GRCh38.p7 | 16:69774938 | CACGCCACAGCACTC[C/T]AGCCTGGGTGACAGA | 11060 |
rs112953546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69862415 | TCACCTAGGCTGGAG[C/T]GCAGCAGCAGGATCT | 11060 |
rs112977401 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69902774 | ACCAAACCAAGACAG[A/T]CGGAGGCTCCATCTA | 11060 |
rs112980521 | snp | A/G | 0.109108 | 0.206518 | intron-variant | WWP2 | GRCh38.p7 | 16:69826263 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAA | 11060 |
rs113004348 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | WWP2 | GRCh38.p7 | 16:69786149 | TGTCTTTTTTTTTTT[C/T]TTCTTCTTTTTTTGA | 11060 |
rs113030950 | snp | G/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69784139 | AGTCTTGCTGTCATC[G/T]CCCGGGCTGGAGTGC | 11060 |
rs113051851 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | WWP2 | GRCh38.p7 | 16:69813098 | TGTGTGTAGGTATGT[A/G]TTATCAGCTTCTACT | 11060 |
rs113061460 | in-del | -/T | 0.106278 | 0.204558 | intron-variant | WWP2 | GRCh38.p7 | 16:69879993 | TATAAAATGAGATAC[-/T]TTTTTTTTTTCTTTA | 11060 |
rs113070976 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69843108 | CTTGACTGCTTTTTT[-/G]TATGTCCGGGGCTGC | 11060 |
rs113126692 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785202 | TGTGCTACTGTACCA[C/T]TCCAGCTTAGGTGTG | 11060 |
rs113131268 | snp | G/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69823285 | GCCTCAGGTGTGTCT[G/T]TCTGACACACAGCAC | 11060 |
rs113143341 | in-del | -/AAAAC/AAAACAAAAC/AAAACAAAACAAAAC/AAAACAAAACAAAACA/AAAACAAAACAAAACAAAACA/AAAACAAAACAAAACAAAACAAAACA/AAAACAAAACAAAACAAAACAAAACAAAACA/AAAACAAAACAAAACG | 0.712629 | 0.129654 | intron-variant | WWP2 | GRCh38.p7 | 16:69851983 | AGCGAGATTCCAGCT[lengthTooLong]AAAACAAAACAAAAC | 11060 |
rs113171797 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69864892 | GTTGGGGTTACAGGC[A/G]TGAGCCACCACGTCC | 11060 |
rs113184354 | snp | C/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69929961 | AATAAGTGACCTCTC[C/T]GTGCTGCAGAACTGT | 11060 |
rs113191277 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812183 | TTTTTTTTTTTTTTT[C/T]TGAGATGGAGTCTCG | 11060 |
rs113206738 | snp | G/T | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69893826 | TGGGATTACAGGAGT[G/T]AGCCACTGCACCCAG | 11060 |
rs113235193 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773095 | TGGCCTCTGGGAAGA[C/T]GCTAGTGTCGCTACT | 11060 |
rs113247154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69929099 | GGTTAGGGACTGCCC[A/G]GCTTCCATGCTGCAC | 11060 |
rs113267902 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774520 | ACTTGGCCTCCTAAG[A/G/T]TGCTGGGATTACATG | 11060 |
rs113272582 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69833074 | TTGTTGCCCAGGCTG[C/G]TCTCAAACTCTTGGA | 11060 |
rs113288587 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69834052 | ACCTGGTCTTGTGTA[C/T]CTCAGCCCTTCTCCT | 11060 |
rs113289098 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69820961 | CCTCGGAGGCTGACA[C/G]CAGGACCAGTGTGGT | 11060 |
rs113289494 | snp | A/C | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69805437 | TTTGCATAAAACTTT[A/C]TGTTTTAGTGGTGAT | 11060 |
rs113297490 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69779652 | AAACTGCTACAGTTC[A/G]GGAGAACAAGATAGT | 11060 |
rs113299486 | snp | A/G | 0.444444 | 0.157135 | intron-variant | WWP2 | GRCh38.p7 | 16:69769038 | AAGAAATGAGTGCAG[A/G]CTGGGCGCAGTGGCT | 11060 |
rs113299983 | snp | C/T | 0.449726 | 0.150364 | intron-variant | WWP2 | GRCh38.p7 | 16:69785719 | GCAACCTCCACTTCC[C/T]GAGTTCAAGCGATTC | 11060 |
rs113302438 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69783847 | ATAGTCCCAGCTACT[C/T]AGGAGGCCAAGGTGA | 11060 |
rs113344960 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69851262 | GACTCAAGTGATCCA[C/T]GTGCCTTGGCCCTCA | 11060 |
rs113345465 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837847 | CTGCGTGATGGGTCT[A/G]TGGCTTACCTTGGAA | 11060 |
rs113351541 | snp | A/G | 0.449853 | 0.150196 | intron-variant | WWP2 | GRCh38.p7 | 16:69785726 | CCACTTCCCGAGTTC[A/G]AGCGATTCTCCTGCC | 11060 |
rs113357379 | snp | C/T | 0.120579 | 0.213893 | intron-variant | WWP2 | GRCh38.p7 | 16:69806957 | ATTTATTTATTTATT[C/T]ATTCATTCATTCATT | 11060 |
rs113368526 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839643 | TTTTCAGGATTGAAA[A/T]TTTTAAAAAACAACA | 11060 |
rs113400146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768115 | GTGTTTGGGGTTACA[A/G]GTGTGAGCCACCACA | 11060 |
rs113420661 | snp | A/G | 0.172674 | 0.237741 | intron-variant | WWP2 | GRCh38.p7 | 16:69785080 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCAGG | 11060 |
rs113443102 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916637 | AATGATTGATAGCAG[C/T]GGGAATGATGTTGGC | 11060 |
rs113462782 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69785336 | AAGGGAAAGTTAGAC[C/T]TTTGGAATGCTTTTA | 11060 |
rs113470921 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69913127 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 11060 |
rs113481675 | snp | C/T | 0.5 | 0 | missense | WWP2 | GRCh38.p7 | 16:69888240 | AGGCCCCCGACGCTC[C/T]GCCTGCTGGGTGAGT | 11060 |
rs113483201 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69926151 | AGTGAGTTAAGGGAT[A/G]GACATCCATGACTTA | 11060 |
rs113499099 | in-del | -/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69889100 | GGGAGGATCACTTGA[-/G]GCCAGGAGTTTGAGA | 11060 |
rs113500623 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933023 | ATGTTCCTTTTTTCC[A/G]TGGTGACCTCCTCTC | 11060 |
rs113510390 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WWP2 | GRCh38.p7 | 16:69801575 | GGGATCTCCCTATAT[C/T]GCTCAGGCTGGAGTG | 11060 |
rs113520842 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69833139 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCTC | 11060 |
rs113523697 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69874364 | TGCTGCTGTGAGAAT[C/T]CTGAGGACCAGTTCC | 11060 |
rs113525332 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940788 | CCCACCTGGCGGTTC[C/T]GTGAGCTCAGGCAGG | 11060 |
rs113547936 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | WWP2 | GRCh38.p7 | 16:69769161 | TCTCTACTAAAAATA[C/G]AAAAAACTAGTCAGG | 11060 |
rs113593229 | snp | G/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69857913 | TCAGCCTCCCAAAGT[G/T]TTGGGATTATAGGCG | 11060 |
rs113616767 | snp | A/G | 8.23649e-05 | 0.00641683 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934084 | CTCCTCCATCAACCC[A/G]GACCACCTCACCTAC | 11060 |
rs113621256 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905155 | CACACTGCTTGGCAG[C/G/T]GCTCTCTGAGCCTCT | 11060 |
rs113627729 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829966 | CAGCTAATTTTTTTT[C/T]TTTTTTCAGATAGAG | 11060 |
rs113632338 | snp | C/G/T | 0.000565357 | 0.0168035 | intron-variant | WWP2 | GRCh38.p7 | 16:69929550 | GACTTGGGCTGAGAG[C/G/T]GGGGCCGGGCTGGGC | 11060 |
rs113647242 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69879117 | TCTCTTTTCATAGTA[C/T]TTGATCATTTGTCCT | 11060 |
rs113655777 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | WWP2 | GRCh38.p7 | 16:69850214 | ACACGGTGAAACCCC[A/G]TCCCTACTAAAAATA | 11060 |
rs113656379 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69908654 | TCGCATGTCATCTTT[C/G]ATGCTTCCTGTAAAT | 11060 |
rs113694739 | snp | C/T | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69798608 | ATAACTAAAAAGAGC[C/T]GGAACATCTGCCACA | 11060 |
rs113707256 | in-del | -/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69918846 | TTTTCCTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs113708916 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WWP2 | GRCh38.p7 | 16:69882825 | ATTAGGATTAAAAGT[C/T]AGAGAACATTGGCTA | 11060 |
rs113716592 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761588 | AAAAAAAAAAAAAAA[A/T]ATATCATCTATCTAT | 11060 |
rs113731154 | snp | A/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69834521 | TATTTCATTAAAAAA[A/T]TTTTTTTTAGTTTTT | 11060 |
rs113739407 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | WWP2 | GRCh38.p7 | 16:69771777 | GTGAAGTACACATGT[A/G]TGCTAGGACCCAAGT | 11060 |
rs113793771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925712 | CATCCACCCACCATC[A/G]CTAAAGGAGTGTGAC | 11060 |
rs113797383 | snp | A/G | 0.00067842 | 0.0184052 | missense | WWP2 | GRCh38.p7 | 16:69871905 | CCGTCAAGAACTCAG[A/G]CCACAGTGGCTTGGC | 11060 |
rs113830080 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | WWP2 | GRCh38.p7 | 16:69816991 | TTCCTAGAGTCTCTG[C/G]CCATAACCTCTATAC | 11060 |
rs113831499 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69832052 | CAGGCGGGTCTCGAA[C/T]TCCTGAGCTCAAGCG | 11060 |
rs113847004 | snp | A/C | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69804381 | TTTGTGCCCAGTACA[A/C]ATAGGGATCTAATTC | 11060 |
rs113847187 | snp | C/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69790234 | CCTGGGCAACAAGAA[C/T]GAAATTCTATCTCAA | 11060 |
rs113856240 | in-del | -/A | 0.499 | 0.0223418 | intron-variant | WWP2 | GRCh38.p7 | 16:69797891 | CAAACTCTATCTCAG[-/A]AAAAAAAAAAAAATT | 11060 |
rs113860978 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69876699 | AGTAAGACTTGAAAG[G/T]CAAGATGACTCCTTG | 11060 |
rs113888876 | snp | C/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69902205 | AGACCAGATGATTTC[C/G]TGTCTGATAACATGA | 11060 |
rs113912441 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817783 | CCCACCTCAGCCTTC[C/G/T]GAGTAGCTGAGATTA | 11060 |
rs113940832 | snp | A/C/T | 0.0186374 | 0.095058 | intron-variant | WWP2 | GRCh38.p7 | 16:69877928 | TTCTCCTGCCTCAGC[A/C/T]CCCCCAGTAGCTGGG | 11060 |
rs113948249 | in-del | -/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69869349 | TCTCCCTTTTTCTCC[-/T]TTTTTTTTTTTTGTT | 11060 |
rs113971505 | snp | A/G | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69809209 | TGCAACAGGGCAGTG[A/G]GCTTTTTCTTAGAAA | 11060 |
rs113980202 | in-del | -/T | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69894076 | TTTCAGGTTGCTGCA[-/T]TTTTTTTTTTTTTAA | 11060 |
rs114028911 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69897950 | CAAAAAAAACACAAT[A/G]AAACAATGGCTGCAG | 11060 |
rs114037522 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | WWP2 | GRCh38.p7 | 16:69880972 | AAGCAAAAGAATTTC[C/T]AATTCCTGATCTTTT | 11060 |
rs114092999 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69770301 | CCCAGCCTCTGGGAC[A/G]GGGAGAGGGACTGAA | 11060 |
rs114096596 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69857638 | TTGTGTTTTCAAATG[A/G]CCTTTGAAGGTCAAC | 11060 |
rs114109761 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69804434 | TGATTGGTTTAGCAC[C/G/T]ACTTATTGAATAATC | 11060 |
rs114122393 | snp | C/T | 0.093417 | 0.194889 | intron-variant | WWP2 | GRCh38.p7 | 16:69800083 | TTGCGTCCCAGCGAG[C/T]GTGTTACATGATTTA | 11060 |
rs114152147 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910134 | AACCCCCAACCTATC[C/T]GCCGCACCCTGATCT | 11060 |
rs114158644 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69811630 | TGGTGGGCATGCAAC[A/G]GTAGTCCCAGCCACT | 11060 |
rs114206947 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69843948 | TGATTTTAGCCAATA[C/T]CCGCAGCATCTTAAA | 11060 |
rs114226802 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69796705 | GGTGGCCTCAGTTAA[A/C]CTTGGTCCGTGTGTA | 11060 |
rs114230384 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69763287 | CTTATCTTGACGAAC[C/T]GTAACTAGGTAGGGT | 11060 |
rs114244572 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69889492 | CCATGTGACCTTGGC[C/T]GAATGACTTAGCCTC | 11060 |
rs114249234 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | WWP2 | GRCh38.p7 | 16:69929672 | TGTCTTGAGACTCTC[A/G]CCGTACAGATACACT | 11060 |
rs114260751 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | WWP2 | GRCh38.p7 | 16:69872458 | CCTGACCTTGTGATC[A/G]CCCGTCTTGGCCTCC | 11060 |
rs114334120 | snp | C/T | 0.0941369 | 0.195465 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774498 | CTGGATTCAAGTGAT[C/T]CACCTGACTTGGCCT | 11060 |
rs114334336 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69813718 | TAGTGATCCTCCCAC[G/T]TTGGCGTCCCAAAGT | 11060 |
rs114343887 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | WWP2 | GRCh38.p7 | 16:69844279 | CCATGATGGGCACCT[A/G]GAACTGGAGGAAACA | 11060 |
rs114385366 | snp | A/C/G | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69805637 | TTTTTTTGAGACAGG[A/C/G]TCTTGCTTTGTTGCC | 11060 |
rs114386675 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69892599 | AGTGCAGTTGTGCAA[A/T]CTTGGCTCACTGCAG | 11060 |
rs114419008 | snp | A/G | 0.030665 | 0.119967 | intron-variant | WWP2 | GRCh38.p7 | 16:69832590 | TCCATCACTCAGTCC[A/G]GAGTGCAGTGACATG | 11060 |
rs114457970 | snp | A/G | 0.00546185 | 0.0519721 | intron-variant | WWP2 | GRCh38.p7 | 16:69936464 | TCATGTGAGTCTCAG[A/G]CGCCGGGGGCTCCGC | 11060 |
rs114458380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69783561 | CTAAATAGTAATAAT[A/G]ATAATATTGAAGAAA | 11060 |
rs114471189 | snp | C/T | 0.039522 | 0.134904 | intron-variant | WWP2 | GRCh38.p7 | 16:69896182 | GCTGGAGTATAGTGG[C/T]GTGATCATAGCTCAC | 11060 |
rs114476301 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69901793 | AGGGCCACTTGAAAA[G/T]AATTGCTGTTAGCCA | 11060 |
rs114495266 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69793048 | GTGGGTTCTTCTTGC[C/T]CACTGCACAGATAAA | 11060 |
rs114568279 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69897954 | AAAAACACAATGAAA[A/C]AATGGCTGCAGTAAA | 11060 |
rs114580655 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69861063 | CCAGCCCCATGGAGA[C/T]TCCTCCTGTGCACAG | 11060 |
rs114599537 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69853698 | ACTAGCCTTGGGCAG[C/T]AGCGAATAGAGAGGA | 11060 |
rs114611281 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69799617 | GTTGAATGAAACTGT[A/C]AAATACCTCTAGCCT | 11060 |
rs114634015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69828432 | AGTACAACAGCGCGA[C/T]CTCAGCTCACCACAA | 11060 |
rs114645708 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69897130 | TTTTGTTTTTGAGAC[A/G]GAATCTGTGTCACCC | 11060 |
rs114701057 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69801750 | ATTTTTGAGCTTTTA[A/T]ATTTTATCTTTTAAA | 11060 |
rs114735867 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69935268 | TAAATATGGCCGGCC[C/T]TTCCCATCGTCGAGG | 11060 |
rs114766037 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | WWP2 | GRCh38.p7 | 16:69917175 | GTAACTGAAAATTCT[A/G]GATATCAATCCTGAT | 11060 |
rs114769086 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69938601 | GCAGTGAGCTGGACC[A/G]TGCCACTGCACTCCA | 11060 |
rs114791963 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69824044 | GCCTGAATGTGAGCT[A/G]TTTCCTTCCCCTTGC | 11060 |
rs114802511 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69764128 | TCAGAGCTAGTAAAT[A/G]AGTAGGGACTCAAGC | 11060 |
rs114807201 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69771226 | ATGTGTAGTTGTTTT[C/G]TCCTGTCAAAAGTTC | 11060 |
rs114900391 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69894858 | GTCCCACACACACAG[A/G]GGCACATTATTTTGC | 11060 |
rs114921414 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | WWP2 | GRCh38.p7 | 16:69927481 | TCCTAAAATGAGGTC[A/G]AGCCAGGTGTTCCTG | 11060 |
rs114980186 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69889695 | TGAAGTCCCTTCTTC[A/G]CAGCTCTGATCATGG | 11060 |
rs115163254 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69904749 | AAATATGAAGATCTC[C/T]CTTTTGCAGTGGGAG | 11060 |
rs115209848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866642 | CCTGTGTCAAAATTT[C/T]CTTCCTTTTTAAGGT | 11060 |
rs115266115 | snp | C/T | 0.021333 | 0.101051 | intron-variant | WWP2 | GRCh38.p7 | 16:69859370 | CCAGCCTAAGCAACA[C/T]AGCCAAACCCCATCT | 11060 |
rs115291707 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | WWP2 | GRCh38.p7 | 16:69916638 | ATGATTGATAGCAGC[A/G]GGAATGATGTTGGCC | 11060 |
rs115298473 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | WWP2 | GRCh38.p7 | 16:69877235 | AGCTTGCTGCAGCTT[C/G]TTCCTCAGCATTTTC | 11060 |
rs115316061 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | WWP2 | GRCh38.p7 | 16:69917988 | AGCAGGGAAAACAGC[A/G]TCTGGCAACGTCAGT | 11060 |
rs115327034 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69844719 | CATTCAGTGCTAGTT[A/C]GTTACTGGTGAGCAA | 11060 |
rs115351511 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | WWP2 | GRCh38.p7 | 16:69911963 | TCTGGAAAGCCTCAG[C/T]GATTAGAGGCACCAA | 11060 |
rs115351778 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69892580 | ACTCTGTCACCCAAG[C/G]TGGAGTGCAGTTGTG | 11060 |
rs115456210 | snp | G/T | 0.040671 | 0.13668 | intron-variant | WWP2 | GRCh38.p7 | 16:69918484 | GTTTACATATTAATG[G/T]TGGCTGCTTTCGTGG | 11060 |
rs115492554 | snp | A/G | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69794161 | GGTCTCAAGTGATCT[A/G]CCTCCCTTAGCCTCC | 11060 |
rs115500566 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | WWP2 | GRCh38.p7 | 16:69903091 | TCTTCTCGCTAAGCC[A/G]GTTGAGGGGGTTCAT | 11060 |
rs115515767 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69926397 | GTTTGGTGGTGTTGA[C/G]AGATGGTGTGAAACT | 11060 |
rs115520817 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924058 | GCTTCCCCCACCTCC[A/G]TGCACTTGCATTCTG | 11060 |
rs115528080 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | WWP2 | GRCh38.p7 | 16:69869037 | GGGATTATAAGCGCT[C/T]ACCACCATGCCTGGC | 11060 |
rs115532409 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69823536 | GTGCAGTGGTGCGGT[C/T]TTGTTCACTGCAGCC | 11060 |
rs115563776 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69815948 | TTTCTTGTAGAGTCA[A/G]GGTCTTACTATGTTG | 11060 |
rs115578896 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69875050 | TTACAGCAAAAGTAT[A/G]TATCTCATAAGTTGT | 11060 |
rs115591694 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69795709 | CACCCAGGCTGGAGT[A/G]TGGTCTCAGCTCACT | 11060 |
rs115595298 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | WWP2 | GRCh38.p7 | 16:69856316 | GAGGAGGGATTGACT[A/G]CAAAGGGGCACAAGG | 11060 |
rs115597327 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69833716 | GCTTTCTTGCTGAAA[C/T]CTGAGCCTCTTGCCA | 11060 |
rs115717950 | snp | C/G | 0.121717 | 0.214577 | intron-variant | WWP2 | GRCh38.p7 | 16:69796037 | TTTTTTTTTTGCGAT[C/G]ATGGGCATCGATAGG | 11060 |
rs115718650 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69876312 | TAAGGCAGTTATAGC[C/G]TTATAAAATGTATTT | 11060 |
rs115738292 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69811531 | GGTGGGAGGCCCTCT[C/T]GAGCCTAGGAGTTTG | 11060 |
rs115740373 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | WWP2 | GRCh38.p7 | 16:69935160 | AGCTGGAGATGTTTC[A/G]ATTCTCCTTTCCTTC | 11060 |
rs115742875 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910130 | CTGTAACCCCCAACC[C/T]ATCCGCCGCACCCTG | 11060 |
rs115756693 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | WWP2 | GRCh38.p7 | 16:69818655 | GATTGGACACAATGA[A/G]TCGATCCTTCCTGCT | 11060 |
rs115884648 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69911382 | AGGAGGCCTCACAGA[A/G]GGAAGTGGCTCCAAC | 11060 |
rs115888878 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838113 | TGAATGAGAAGTTAG[A/G]CCAAGAGGAATTAGG | 11060 |
rs115890606 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69872137 | AGCCAAGGTTATTCT[C/G]CATATGACTGCGCTC | 11060 |
rs115909198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69927666 | CCTTAACAGGGCAGA[C/T]GTGGAGGATCTAGTT | 11060 |
rs115913564 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69899221 | TAAGTTACATAAAAA[C/T]GTTACAGGCCACACT | 11060 |
rs115948668 | snp | A/T | 0.126219 | 0.217206 | intron-variant | WWP2 | GRCh38.p7 | 16:69801230 | AATTAATTTTTATTT[A/T]TATATATATATATTT | 11060 |
rs116019867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918624 | TAGCTGAGCCTCCTT[C/T]TTTCTGATGCTTGAT | 11060 |
rs116028824 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69807940 | CAGCCTGGGTGACAG[A/G]GCAAAACCCTATCTC | 11060 |
rs116057237 | snp | A/T | 0.030278 | 0.119257 | intron-variant | WWP2 | GRCh38.p7 | 16:69832982 | GCCTAGCCTCCCATG[A/T]AGGTGGGACCGCAGG | 11060 |
rs116067210 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | WWP2 | GRCh38.p7 | 16:69775026 | CAAATTTATATCATA[C/T]AAATTTACGTGACTA | 11060 |
rs116082496 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69827062 | CTCCCATCTTTTGGG[A/G]AAGTATTTGCAAGAA | 11060 |
rs116098479 | snp | A/G | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838652 | CAGGGATGGCAAGAG[A/G]TGGCTGGGGGTTGAA | 11060 |
rs116100564 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69780543 | CGTCTTTAACTCTGC[C/T]GGAGGTTGTCAGCTG | 11060 |
rs116123798 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | WWP2 | GRCh38.p7 | 16:69886418 | TAGAGATGGGGAGAC[C/T]CAGACCAGGTAATAG | 11060 |
rs116143408 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933370 | GGGAACGGGGATGGT[A/G]TTGGGGTCTGGGGGT | 11060 |
rs116162199 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69842482 | ATTCTTGCTCCTCTC[C/T]CTCCTTGTTTTTGGA | 11060 |
rs116208196 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69776331 | CTTCCCACAACTAGA[A/G]CTAGGAGGGAATCTT | 11060 |
rs116236508 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69858745 | TTGGGAAAAGAAGGT[A/G]TAAAGTCCGTGTACT | 11060 |
rs116246542 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69911476 | AAAGGATGTGTTTGG[A/G]GAAGGATGCATGGGG | 11060 |
rs116247934 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | WWP2 | GRCh38.p7 | 16:69917520 | TCCCCAAATTAGAAA[C/T]TGAGAGCTAATGGCA | 11060 |
rs116301857 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69936696 | CTTCAAGCCTGCAGC[A/G]TGGAATTTCTTTGAA | 11060 |
rs116329857 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WWP2 | GRCh38.p7 | 16:69919483 | ACATTTAAATTTTCT[C/T]GTCCAGAATTGTGGG | 11060 |
rs116332046 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69848201 | GCTGGGTGTAATCCC[A/C]GCGCTTTGGGAGGCT | 11060 |
rs116390682 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69902932 | GAGGGAGGAGTGAGG[G/T]TCTGTGAGAAAGGGA | 11060 |
rs116405057 | snp | A/G | 0.110519 | 0.207473 | intron-variant | WWP2 | GRCh38.p7 | 16:69857385 | GGTGTGAGCCACCAC[A/G]CCTGGCGTAACTTTC | 11060 |
rs116405249 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69811818 | AGAACTCCTCAATGT[C/T]GTCCTTCACCCAACT | 11060 |
rs116459616 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69882796 | TTTGGGGAGATATGG[A/G]TGTACATCAAATAAT | 11060 |
rs116488447 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | WWP2 | GRCh38.p7 | 16:69825573 | TTTTTATTTTGAAAG[C/G]TAATATTATTTATTG | 11060 |
rs116492386 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69765751 | ATTGCTTGAGCTCGG[G/T]AGATGGAGGTTGCAG | 11060 |
rs116544537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926009 | AGAGGGAAGCAGATA[C/T]GAGAGTTGAATGCCA | 11060 |
rs116632810 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69857240 | TCCCGAGTAGCTGGG[C/T]GCGCTCCACCACGCT | 11060 |
rs116637588 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | WWP2 | GRCh38.p7 | 16:69851271 | GATCCACGTGCCTTG[A/G]CCCTCACATGTATCC | 11060 |
rs116649414 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69847934 | AAGTTGGAATGAAGC[C/T]CACAGGACTGTCTGT | 11060 |
rs116653642 | snp | C/T | 0.0271762 | 0.113356 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69840009 | CAAAATGTGAAGATG[C/T]GGAGAAAGCATTCCC | 11060 |
rs116666816 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69769675 | AGAGCTCTTACTGTG[C/T]GTCCTCTGCTTTACC | 11060 |
rs116716684 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69862887 | CTTGCCACTATACCT[G/T]GCTAATTTAAAATAA | 11060 |
rs116733038 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69882350 | GTTTTTAATTTTTTT[A/T]ATTTCTTTTCTTTTC | 11060 |
rs116734578 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69921635 | GTTTGCTTGCTTCAC[C/T]GTTGCAGTTTCTTTT | 11060 |
rs116734772 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69843583 | AAAATCTTCCCAAAC[A/G]AGGCCAGGCACAGTG | 11060 |
rs116793006 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773187 | ATACACGTTGCTCCT[C/T]TTTTTTTTTTGAGAT | 11060 |
rs116809197 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69763688 | TAAAACAATTTATTG[C/T]TCTTTCTTGTTTGCT | 11060 |
rs116857982 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | WWP2 | GRCh38.p7 | 16:69874962 | AGGAGGCAGATGTTG[C/T]AGTGAGCTGAGATGG | 11060 |
rs116897251 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | WWP2 | GRCh38.p7 | 16:69882068 | CAAATGATCCACCTG[C/T]TTTGGCCTCCGAAAG | 11060 |
rs116903569 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | WWP2 | GRCh38.p7 | 16:69874295 | CCCCTCTTCAGCAGC[C/G]CAGGACCAGAGGGGG | 11060 |
rs116910969 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69933691 | GGATATTGTGATGTA[A/T]AGTCTTGGAACACAT | 11060 |
rs116934842 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69852418 | AGTAGCTGGGTGGCA[C/G]CTGCCACCACGCCCA | 11060 |
rs116986479 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69898000 | CCTTTTTGTGTATGT[A/G]GTTTTTTCTTTTTCT | 11060 |
rs116995560 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69844695 | TTTTGGCCCATCACA[C/T]GTGGTAGACATTCAG | 11060 |
rs117001329 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | WWP2 | GRCh38.p7 | 16:69821345 | GAAAGAAAAGGTCCT[G/T]TTAGCCACAAGTTTC | 11060 |
rs117016888 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69916627 | AGTCAGGCTGAATGA[C/T]TGATAGCAGCGGGAA | 11060 |
rs117045658 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69792997 | GCCTGGCCTTTAAAC[A/C]GAATCTAATCATGAG | 11060 |
rs117098275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908922 | ATGGCTTCTTGAAAC[A/G]GTCCCTTTCTGCGGA | 11060 |
rs117133291 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69851960 | TGCACTCCAGCCTGG[C/T]GACAGAGCAGCGAGA | 11060 |
rs117186328 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69764593 | AGAATGTGAGTAAAT[A/G]AAGTTTAGAAAACGC | 11060 |
rs117196148 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909986 | ACACATATTTGTTGA[C/T]TTATTGTTTTTGGCT | 11060 |
rs117233720 | snp | A/G | 0.0295035 | 0.117819 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909907 | TCGGCACACTATGAT[A/G]GCCTGTGGACAAAAT | 11060 |
rs117248035 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69853084 | AGTGGATTTTGAGCA[A/G]GGCAATGGTAAGGCT | 11060 |
rs117332082 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | WWP2 | GRCh38.p7 | 16:69904961 | AACCTAACTTAGTAC[A/G]TAAACCAACCAAAAC | 11060 |
rs117332841 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69828863 | TATGCAAACCACCGT[A/G]TGCAGGTGAGCCACA | 11060 |
rs117381867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818002 | GTTTCAAGTTTTTGA[A/T]GCCTGCTGCCTGTGT | 11060 |
rs117386658 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69784142 | CTTGCTGTCATCGCC[C/T]GGGCTGGAGTGCAGT | 11060 |
rs117387107 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69794720 | TCTTTAAAACAGCTG[A/G]TGGAAGTCTTTAAAA | 11060 |
rs117395474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785934 | CACCCAGCCTACCCA[G/T]TTAAATAATTGTATT | 11060 |
rs117397905 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69904965 | TAACTTAGTACGTAA[A/T]CCAACCAAAACCCAA | 11060 |
rs117401335 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910303 | AATATTTGACTTTCT[A/G]TAATTGTGTCACAAA | 11060 |
rs117443900 | snp | A/C | 0.019556 | 0.0969306 | intron-variant | WWP2 | GRCh38.p7 | 16:69937543 | TGACTGCCGCCTCTC[A/C]CCAGCTGATGCTGTG | 11060 |
rs117541452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69850081 | AGGCTCTGAGCTGTC[A/G]TGGTGATTAAAAGAT | 11060 |
rs117541985 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69894460 | CGTTTTAAGAACTGA[A/C]GGCTGCTGAAACCTG | 11060 |
rs117543431 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69928266 | AGAGCCATTAGCATC[A/G]TTTGTTTTCAGGAGA | 11060 |
rs117583475 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69889441 | ATTATAAGCATGGAC[C/T]TGTGAATCAGACAGC | 11060 |
rs117587176 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69849762 | GCAGTGAGTTATGAT[A/C]GTGCCACTGCACTCC | 11060 |
rs117592988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69937357 | ACTTCGGCAGGGCAG[A/T]TGGGTTTGATTTGGG | 11060 |
rs117628648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69799938 | CCCTCCTTCATAAGG[C/T]CTCTATTCAGAGCAG | 11060 |
rs117631037 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | WWP2 | GRCh38.p7 | 16:69921516 | CTGCCTCAACACACA[C/T]CTTCTCCAGTTCCTC | 11060 |
rs117637107 | snp | A/C/G | 0.00207458 | 0.0321409 | missense | WWP2 | GRCh38.p7 | 16:69936391 | AAGGTGACGACCCAC[A/C/G]AGCTGAAGGAGGGCG | 11060 |
rs117642783 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69929303 | GACAAGTGTGAGTGA[A/G]CTTGGCTTTGGCTGG | 11060 |
rs117681793 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69851335 | CCCTGTGCTTCATCT[A/G]TTCATCTCTCCCTCC | 11060 |
rs117686760 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | WWP2 | GRCh38.p7 | 16:69829170 | TTTTGCAAGTCTGCC[C/T]ACTTCTTCAGCTCCA | 11060 |
rs117692719 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923883 | ACTTGGATTTTATGA[A/G]ATGCTGTACCCTATC | 11060 |
rs117709675 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | WWP2 | GRCh38.p7 | 16:69854840 | ACAAGTGTGGGCCAC[C/T]GCGCCTAGCCTCTTT | 11060 |
rs117727494 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69882804 | GATATGGGTGTACAT[C/T]AAATAATTAGGATTA | 11060 |
rs117730544 | snp | A/T | 0.0107246 | 0.0724382 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940385 | CTTTGCCAGCAAAGG[A/T]GGTTCTGCCTGTAAT | 11060 |
rs117731745 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69874784 | AGAAGTTGCATCAGC[C/T]GTGGTCAGATTCCGA | 11060 |
rs117775035 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909866 | TATCAACTCATGGCG[A/G]GTTTTGTTTCATCTG | 11060 |
rs117831368 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WWP2 | GRCh38.p7 | 16:69899838 | TAATAATCTTACAAT[C/T]GATGGCATTTTAGAT | 11060 |
rs117849002 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69794063 | GCTGGAACTACAGGC[A/G]TGCGCCACCACGCCC | 11060 |
rs117855256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833576 | TTACTGCTGTCTGTC[C/G]ACCTCCATAAAGTAG | 11060 |
rs117860239 | snp | A/C/T | 0.000282458 | 0.0118808 | intron-variant | WWP2 | GRCh38.p7 | 16:69937497 | GTGCTAGCGAGTGGA[A/C/T]GATGCGCGGGGAGGG | 11060 |
rs117869518 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69781013 | ATCCTGGGTGACAGG[A/G]CTAGACCCTGTCTCA | 11060 |
rs117870851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69790069 | CCAATGTGGTAAAAC[C/T]CTGCCTCTACTAAAA | 11060 |
rs117888798 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WWP2 | GRCh38.p7 | 16:69875834 | CCCTCAGAGCCATCT[A/G]TCAGGGTTTGAGCTT | 11060 |
rs117917700 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69784482 | AGAAGCAAAGGTGAG[A/T]AAAGCAGTTGGTGCT | 11060 |
rs117961924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913545 | ATGTGAACAAACAGC[A/C]AAAGATGAGCAGACA | 11060 |
rs117994247 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69823887 | CCATTCCTCTTGAGC[C/T]TGTGGCACAGGGGCG | 11060 |
rs118029132 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69898404 | TCAACTTCAGTAGGT[A/G]TTATCAAATTGCCTG | 11060 |
rs118036695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783302 | GGCGTGAGCCACTAC[A/G]CCTGGCCAAGGGCTT | 11060 |
rs118042243 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69902978 | GGATCAGGGAGGACC[C/T]GCAGGGACATTTAAT | 11060 |
rs118074110 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69890197 | CACTTTCAAAAACCC[A/G]GTTGTCAAAACAAAA | 11060 |
rs118085733 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69907033 | ATGTTAAATGATTAC[A/G]AAATAGATAACACTA | 11060 |
rs118086566 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | WWP2 | GRCh38.p7 | 16:69831985 | AGGCAGGTACCACCA[C/T]GCCCAGCTAATTTTT | 11060 |
rs118118900 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69814204 | CTTGCTCTGTCGTCT[A/G]GGCTGCAGTGCAGTG | 11060 |
rs118147165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767599 | CGTTGCAAGAAAGCA[A/G]TGGGCAGCACAGCAG | 11060 |
rs118165329 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | WWP2 | GRCh38.p7 | 16:69908624 | GCAGGAACTGGCTTC[A/G]CCATTGGGTCGGCCT | 11060 |
rs118166554 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WWP2 | GRCh38.p7 | 16:69917308 | GTCCAAAATAATAGC[C/T]AGTGGCCCCCAGGAC | 11060 |
rs137856053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69888433 | TCTTAAAAAGAATCT[C/T]AGTCGCCTGGGGCAG | 11060 |
rs137862538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69868528 | CTCCCTGAGGGGTCC[A/G]GCTTGCTCCTGGGGG | 11060 |
rs137868855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802507 | TAGTGGAACCATACA[G/T]TATTTGTCCTTTTAT | 11060 |
rs137870317 | in-del | -/TTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885142 | ACACACACACACACA[-/TTC]TTCTTCTTTAGAATG | 11060 |
rs137933573 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69836245 | CACAATTCACGCATG[G/T]CATTTGTTGGTTTTC | 11060 |
rs137975713 | snp | A/T | 0.00341846 | 0.0412013 | intron-variant | WWP2 | GRCh38.p7 | 16:69939807 | GAGCCCTGGCCTCCT[A/T]GGGCTGACTGTCGTG | 11060 |
rs137979638 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69833508 | CTGTCTTTCAAAGGG[C/T]ACAGTCCCTGGGGAC | 11060 |
rs137985423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69774899 | CACTTGAATCTGGGA[A/G]GTGGAGGTGCAGTGA | 11060 |
rs137987086 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923571 | CCCCTGTGGAAGCTG[G/T]GTTGGTACCAGCTGG | 11060 |
rs137990371 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795269 | CGGATACACACACAC[-/CA]ACACACACACACACA | 11060 |
rs138011584 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | WWP2 | GRCh38.p7 | 16:69871122 | AAGACCCCATCTCCC[C/G]AAAAATAAAAAAATG | 11060 |
rs138017643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808300 | ATAGAGATGGGATCT[C/T]GCTATATTGCCCAGG | 11060 |
rs138021233 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778073 | GAAACCCTGTCTCAA[-/AT]ATATATATATATATA | 11060 |
rs138043790 | snp | A/G | 3.36797e-05 | 0.0041035 | intron-variant | WWP2 | GRCh38.p7 | 16:69936031 | GCTGATAGGAGGGAC[A/G]TCTCTGGGTGGGAAG | 11060 |
rs138051944 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69869123 | GAACTCCTGACCTCA[C/G]GTGATCCACCTGCCT | 11060 |
rs138123198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812734 | TTCTTGGCAGGAACA[C/G]CCAGGAGTGACTTTG | 11060 |
rs138139651 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69845666 | CTGAGGGGTTCATTC[A/G]TCCAAGCTCATCCCG | 11060 |
rs138149477 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69781148 | GGAAAAAAAAAGAAC[A/T]GAGATGGGAGTCTGT | 11060 |
rs138164191 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69849666 | AAGTAATCATGGCTG[A/G]GCATGGTGGCTGTAT | 11060 |
rs138189714 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69786481 | TTTGAGATGGAGTTT[C/T]GCTCTTGTCACCCAG | 11060 |
rs138197201 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69878377 | TGTAAAAAATCACAT[A/G]GTGCAACTCAACAAA | 11060 |
rs138206003 | snp | C/T | 0.102014 | 0.201495 | intron-variant | WWP2 | GRCh38.p7 | 16:69778108 | ACACACACACACACA[C/T]GTATATACATACACA | 11060 |
rs138223914 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69794559 | CTATAAACTAAATTT[C/T]TCCCAAAATTAGCTT | 11060 |
rs138241293 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831827 | GGAAAAAAACAAAAC[C/T]TTTTTTTTTTTTTTT | 11060 |
rs138252641 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69784260 | GCCCACCACCATGCC[A/C]GGTTAATTTTTGTAT | 11060 |
rs138265248 | in-del | -/CCCCCCCC | | | frameshift-variant | WWP2 | GRCh38.p7 | 16:69888056 | ATGATGAACCCACAA[-/CCCCCCCC]CAGCCACTGATCCCG | 11060 |
rs138285181 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | WWP2 | GRCh38.p7 | 16:69854892 | ACAGGGTCTTGTTCT[A/G]TCATCCAGGCTAGAG | 11060 |
rs138285985 | snp | A/G | 0.000586542 | 0.0171151 | missense | WWP2 | GRCh38.p7 | 16:69842078 | TAGCTCCAGAGAACC[A/G]GCACCAGCCCCCCAG | 11060 |
rs138291008 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | WWP2 | GRCh38.p7 | 16:69788417 | GAAGCTCCCATGTGA[C/T]GTGACCCTTCCCCAC | 11060 |
rs138306908 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69882317 | GTTTTATTTCAAATA[C/T]CTTTCTTTTATTTTT | 11060 |
rs138329886 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69798213 | GTTCGTATCCTTTGG[A/G]GGAATACTCAAGAAA | 11060 |
rs138363713 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69835775 | TGCGTCTCCCAAGAA[G/T]AAGACATGCTCATAT | 11060 |
rs138372073 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69879690 | AGAACTTGGCTGTAC[A/C]AGTATCTGAGCCCAA | 11060 |
rs138376334 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917621 | TGACAGGGCCTGCCC[A/G/T]GCTGTGCTAGGCATC | 11060 |
rs138379561 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69906354 | TGGGATTACAGGTGT[C/G]AGCCACCGCACCCGG | 11060 |
rs138431051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912226 | CCCCAGCGGCGGAGG[C/T]TACAGTGAGCTGAGA | 11060 |
rs138500614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828793 | TTAAATATGGGAGTT[A/T]CCTATTATTCCATCC | 11060 |
rs138515100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773040 | TGTATGTGTAGTCTG[C/T]TCTGTGTATTGAGAG | 11060 |
rs138529923 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69928324 | CCTGGGAAAGGTGAC[C/G]TCTTTTGAGCCAAGA | 11060 |
rs138546491 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69769416 | TAATTAGAAATAAAA[A/T]CTTTGTGAACCCATG | 11060 |
rs138547366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807512 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGTCGGG | 11060 |
rs138567227 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69841758 | ATAAGGCAATGTGCT[C/T]GTAAGTGCCTTGGAT | 11060 |
rs138573051 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69777323 | TCTTTTTTTTTGAAA[C/T]GGAGTCTCATTCTGT | 11060 |
rs138585070 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69868957 | CAGTGGTACAATCTC[A/G]GCTCACTGCGACCTC | 11060 |
rs138605619 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69876252 | CTTAAGCCTTTAGGA[G/T]GTTTTTAATGGGTTT | 11060 |
rs138633342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866061 | GACCTCGCATCTCAT[A/C]ATGGCTGGGAATTAA | 11060 |
rs138661773 | snp | C/T | 0.000115316 | 0.00759243 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931154 | TTGCTCTTCCTAGGA[C/T]GAAGCAAGGTTCCCC | 11060 |
rs138686396 | snp | C/T | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69897644 | GCCAGGCGCAGTGGC[C/T]CACGCCTGTAATCCC | 11060 |
rs138691725 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781547 | AGAGATGGAGTTTGA[C/T]CATGTTGCCCAGGCT | 11060 |
rs138713393 | in-del | -/TTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778954 | CTGGCCGGTTATTTA[-/TTTA]TTTATTTATTTTTTG | 11060 |
rs138734512 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69879308 | GGTAACTATAACCAC[C/G]AGTGTCCATTTCCAG | 11060 |
rs138738859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817202 | ACCCAGTTTTTTCCG[C/T]ATCAGTGAAACTAGG | 11060 |
rs138762665 | snp | C/T | 6.29465e-05 | 0.00560975 | missense | WWP2 | GRCh38.p7 | 16:69939060 | AACGAGAAGAGGATC[C/T]GGCTGCTGCAGTTTG | 11060 |
rs138788618 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69912106 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTG | 11060 |
rs138835058 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69791130 | TTAGCAAGTCTAGGT[C/G]AAAGCAGAAGTTGGC | 11060 |
rs138864795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854522 | TCAAACGTTGAATCA[A/G]TTCTGTATGTAGGCT | 11060 |
rs138867319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69788007 | TCCTGTCCTGTCTCT[C/T]GGCTTCTGCACTTTG | 11060 |
rs138907460 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69822105 | CTCGTGGGCTCAAGC[A/G]ATCCTTCCACCTCAG | 11060 |
rs138920990 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69907824 | AGTATAAAATAACCA[G/T]ATGTTGTGTTTCTGT | 11060 |
rs138927140 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69808708 | CGCCCGGCCATGGCC[G/T]GTCTTTGTATTTGGG | 11060 |
rs138927446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849261 | AGGAGCTGAGCCTTG[A/G]GCACTAGGCCATTCT | 11060 |
rs138940898 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69858198 | GAATTGGAGACTTCC[A/G]AGGAGTTATTTCTTC | 11060 |
rs138973751 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882802 | GAGATATGGGTGTAC[A/G]TCAAATAATTAGGAT | 11060 |
rs138986579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905837 | AAGCATGGTGAAACT[C/T]ATGGGCTTGGGGGGC | 11060 |
rs138991443 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69815122 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGA | 11060 |
rs138994855 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845982 | CTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 11060 |
rs139045758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910559 | GGATTACAGGCGCCC[A/G]CCACTATGCCCAACT | 11060 |
rs139048732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850489 | TCTAGTGTGATGGAT[C/G]CATGGTGATGGTATG | 11060 |
rs139052693 | snp | A/G | 6.58913e-05 | 0.00573945 | missense | WWP2 | GRCh38.p7 | 16:69888083 | CCCGAAGAACCTTCC[A/G]TTGTTGGTGTGACGT | 11060 |
rs139057990 | snp | A/G | 0.0566069 | 0.158427 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760415 | CTCACTGCCACCTCC[A/G]CCTCCCGGGTTCAAG | 11060 |
rs139088282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862237 | TGCCCGGCTAATTTT[A/G]TATTTTTAGTAGACA | 11060 |
rs139091143 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69795834 | TGTATTTTTGGTAGA[G/T]ACAGGGTTTAGCCAT | 11060 |
rs139105338 | snp | A/G | 0.000181856 | 0.00953388 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931833 | CCTATGACCTGCGCC[A/G]CCGGCTCTACATCAT | 11060 |
rs139153972 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762188 | GGTGAGCAGAAACCC[G/T]TCCACTTTCAACTAC | 11060 |
rs139189289 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887121 | TGATCATCAAAGAGG[A/T]GAAGAGATGGTGAAA | 11060 |
rs139194676 | in-del | -/AG | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69853961 | CTGGCTCTGGGGCAG[-/AG]TCATTTCTCTGAAAG | 11060 |
rs139197398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69799373 | CAACCTGGTATTGCA[A/G]TTTCCCCCAGGACTA | 11060 |
rs139231490 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837033 | GGCTCAGGTGATTCT[A/C]CCACCTCTGCCTCCT | 11060 |
rs139282478 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69795031 | TTGAGCCCAGGAGTT[C/T]GAGATCAGCCTGGCC | 11060 |
rs139324402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932883 | AGAGCGCTGTGGCCC[A/G]CAGCGACCTCTCCGC | 11060 |
rs139335579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842774 | TCCTGGGCTCAAGCA[A/G]TCCACCCACCTCAGC | 11060 |
rs139337909 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69765677 | CAAAATACAAAAATT[A/G]GCTGGGCTTGTTGGC | 11060 |
rs139338810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69778788 | CTGGGATTATAGTTG[C/T]GCCACCACTCCTCGC | 11060 |
rs139343045 | snp | A/C/G | 0.0119155 | 0.0763244 | intron-variant | WWP2 | GRCh38.p7 | 16:69891735 | TGAGCCCAGTTCTCT[A/C/G]CTGACTCACTACCTG | 11060 |
rs139347335 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69832977 | CTCCTGCCTAGCCTC[C/T]CATGAAGGTGGGACC | 11060 |
rs139349122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792998 | CCTGGCCTTTAAACC[G/T]AATCTAATCATGAGG | 11060 |
rs139368658 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877308 | AACCTCATGAACCAA[G/T]CTTTGCTATCTTCCA | 11060 |
rs139388172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931335 | GTGTCTTAGGCGGGC[A/G]CAAGACACTTGTCTA | 11060 |
rs139415489 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69788566 | GAGTGAAATGCTTTT[C/T]GCTTCATTATTTCCT | 11060 |
rs139455260 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69926740 | TGCCCCACATGGCTC[C/G]CTGGACCAAAGAAAG | 11060 |
rs139469590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886002 | GCCAGATGATCGGGA[A/G]AGGGGGGTTGCCTAG | 11060 |
rs139470941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880681 | TTACGAAATCTTTGT[C/G]CAGTTTTGGTTGCTG | 11060 |
rs139473184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69818670 | ATCGATCCTTCCTGC[C/T]TGACATATGTTCTGC | 11060 |
rs139483912 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69826157 | CTATAATCCTAGCTA[C/T]TCAGGAGGCTGAGTC | 11060 |
rs139504560 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913966 | AATCCCAGCTACTCG[C/T]GAGGCTGAGGAAGGA | 11060 |
rs139510804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830527 | TTAGCAATGATAAAG[A/G]GTAGATTCCCAGCGG | 11060 |
rs139557297 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | WWP2 | GRCh38.p7 | 16:69770061 | GAGATGGGATTTCGC[C/T]GTGTTGGCCAGGCTG | 11060 |
rs139573012 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809791 | AAGAGAGAGAGAGAC[-/AG]AGAGAGAGAGAGAGA | 11060 |
rs139600416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919540 | AACAGTCTCCTATAC[C/T]GTGTCCCTGTGGGAA | 11060 |
rs139607226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919967 | CCTGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 11060 |
rs139615581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833915 | GTCCTGGGGCTTTCT[A/C]ACTCATGCTAGGGAG | 11060 |
rs139620648 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69770711 | TGGGGAACTAAACCT[A/G]TGGGATCTGATGCTA | 11060 |
rs139621116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782004 | TTAAATTTTCGGAGC[C/T]GGGCGAGGTGGCTCA | 11060 |
rs139637867 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849296 | TCATTGTTGGCTGGC[-/G]GGTTGCCACCCCTCC | 11060 |
rs139657103 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69817374 | CCATCTTAGCCTCCC[A/G]AATAGTTGGGATTAC | 11060 |
rs139666354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69869586 | CTTGAGCTCAAGTGC[C/T]GTCCCATCTCAGCCT | 11060 |
rs139667673 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69914525 | CACTTTGGGGGGCCA[A/C]GGCAGGAGGATCGTT | 11060 |
rs139718247 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69813569 | CTGGGTTCAAGCGAT[A/C]CCCCCACCTCAGCCT | 11060 |
rs139745770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909355 | AAGAATCACCTCCCA[A/G]TAAAGTAGCCATGAA | 11060 |
rs139750484 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | WWP2 | GRCh38.p7 | 16:69850356 | CACACCACTGCACTC[C/T]AGCCTGGGCAACAGA | 11060 |
rs139780091 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69906824 | ATCAGAGGCTGTAGT[C/G]AGCTATGATCACACC | 11060 |
rs139833507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69775590 | TAGAGCCCTGAACCT[A/G]GTAATCATAGTTATT | 11060 |
rs139836371 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69810645 | ACTGTGTTAGCCAGA[G/T]AGTCTCAATCTCCTG | 11060 |
rs139890076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906579 | AAAAGTCAGCACGTG[A/G]TGCAAAATTATGCAG | 11060 |
rs139898756 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69798905 | AGGGGGTTGTGGGAG[C/G]TACAGATTCCCTGTG | 11060 |
rs139899699 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761035 | GAGAATTGCTTGAAC[C/T]TGGGAGGCAGAGGTT | 11060 |
rs139901059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809504 | AGGTACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11060 |
rs139901451 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69771407 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 11060 |
rs139927614 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69862705 | TCCAGCCAGCCATGA[A/G]TTCTTTTTTTTTTTT | 11060 |
rs139932753 | snp | A/G | 6.73299e-05 | 0.00580176 | missense | WWP2 | GRCh38.p7 | 16:69871872 | AAAGCCCCGGTGCTC[A/G]GAGCCGGCACCGCCA | 11060 |
rs139933742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69796457 | GGGTACACGGCAGAG[C/T]ATCAATTGTTTGCCC | 11060 |
rs139959670 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69894592 | AGCCAACTGGAAGGG[C/T]ATGAAGTTTTCAGGT | 11060 |
rs139960097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69869908 | GCAGGGTCGTTCTGC[C/T]GGAGGTGGATCCTCC | 11060 |
rs139960563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860449 | CATAAAGGGAACAAT[G/T]AGGATGTTATGAGAG | 11060 |
rs139996375 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69890393 | TTTTGTGAGGTTTTT[G/T]ATTTTAGTGAAGGTT | 11060 |
rs140030827 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69902829 | GAACAGGAATCAGGA[A/G]GCTCGTCTGGTTGGT | 11060 |
rs140093063 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | WWP2 | GRCh38.p7 | 16:69898854 | GATTACAGGCATGTG[C/G]CACCACTCCCAGATA | 11060 |
rs140112590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69784494 | GAGTAAAGCAGTTGG[C/T]GCTAGCACCAATTGG | 11060 |
rs140144428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69782240 | GTGAGCCAAGATAGC[A/G]CCACTGCACTCCAGC | 11060 |
rs140172022 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69844117 | AGATGCCATTTCCCC[A/G]TTCTCTTTTCTCCAA | 11060 |
rs140173830 | snp | C/T | 0.093417 | 0.194889 | intron-variant | WWP2 | GRCh38.p7 | 16:69807524 | CTCGGGAGGCTGAGT[C/T]GGGAGGATTGCTTGA | 11060 |
rs140204619 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69877678 | ATTTAAAGTGAGAGA[C/T]ATATGACTCTTCCTT | 11060 |
rs140209978 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69776957 | CCCTACCTTAGATGG[G/T]ATTGTTGTAGACCAG | 11060 |
rs140228605 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69904990 | ACCCAAATTAGGAGT[A/G]TATGTTTTTTGTAAC | 11060 |
rs140236610 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941944 | TCACCGGCTTCAGCC[C/T]TTGGTCAGCTGCCTC | 11060 |
rs140238234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874675 | TTGAGACTTGTATGG[A/G]ATGATTTACTTGCTA | 11060 |
rs140238862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844904 | GGAAATATTTTTGCA[A/G]ATATTATCCAAAGGC | 11060 |
rs140253209 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69822961 | GGCCAACATGACAAA[C/G/T]CTCCATCTTTACTAA | 11060 |
rs140261430 | snp | C/T | 0.000131887 | 0.00811949 | missense | WWP2 | GRCh38.p7 | 16:69798745 | CCTACGTGGAGGTGG[C/T]GGTGGATGGACTCCC | 11060 |
rs140275189 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69871075 | AGGATCGTTTGAGCT[C/T]AGGAGTTTGAGACCA | 11060 |
rs140306376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919150 | TCCCCGACCACATTT[A/G]AATTTTCTTTTCTTT | 11060 |
rs140311365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69856198 | GCTAAGCTTAAGAAG[C/T]CAGACATAGAAGCTT | 11060 |
rs140316156 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858928 | TGGGCACTGGATCCC[A/C]CAGAGTGATGCCATA | 11060 |
rs140342714 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857797 | CTCCCAGGTAGCTGA[A/G]ACTACAGGTGTGCGC | 11060 |
rs140381297 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855934 | ATAGAACGTTTTGGC[C/T]TTATCTTGTTATTCT | 11060 |
rs140413682 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69849322 | CCTCCTTCCACTGAG[A/G]TGACTAAAGGCTGCT | 11060 |
rs140454288 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69824120 | CCGCACCAGTCATTC[A/G]GGCGGCTTCCGCCTG | 11060 |
rs140464457 | in-del | -/TTC | 0.487432 | 0.0782705 | intron-variant | WWP2 | GRCh38.p7 | 16:69800177 | GCCTCCTCTGGTCTT[-/TTC]TTTTCGGCTGGGCAC | 11060 |
rs140490016 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | WWP2 | GRCh38.p7 | 16:69832049 | GCCCAGGCGGGTCTC[A/G]AACTCCTGAGCTCAA | 11060 |
rs140513228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883985 | ATAGTTATATGTTAC[C/T]AAAACTTTAAAAAAA | 11060 |
rs140516280 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69920114 | GACCCCCGACTTTTA[A/G]TCATCAGCCATAAGT | 11060 |
rs140520717 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69820753 | TAGAATGTAAGGTCT[A/G]TGGGGGCAGGCGTTT | 11060 |
rs140520779 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69861011 | AAGAGGCTTTTCTGG[C/T]GCACCTGTACAGGTT | 11060 |
rs140593726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835495 | CCCAATGTTTAATTA[C/T]GAAATTTGCAAACAT | 11060 |
rs140597563 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772746 | GTGCTTTTGGTGCCT[C/T]TTCCCTGTTTCAGCC | 11060 |
rs140641016 | snp | A/C/T | 0.00508863 | 0.0501851 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939080 | GCTGCAGTTTGTCAC[A/C/T]GGTACCTGCCGCCTG | 11060 |
rs140645449 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69870548 | TCAAGTGATCCTCCC[A/G]CCTTGGCCTCCCAAA | 11060 |
rs140670974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69806621 | CAGCTTCTTTGTTTC[A/G]TCTTGACTCAATTTT | 11060 |
rs140681818 | snp | G/T | 0.0744748 | 0.178019 | intron-variant | WWP2 | GRCh38.p7 | 16:69823598 | TCAGCCTCCCAAGTA[G/T]CTGGGATTACAGGTG | 11060 |
rs140731064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69901995 | TATCTAAAATTCACT[C/T]GAACTCTTTGCCCAG | 11060 |
rs140738594 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69842514 | TCCCCAGTGTTTATT[A/G]TTTCTATCTTTGTGT | 11060 |
rs140738693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800357 | TGATCATCAGGGAGA[A/G]TTCTATTTATTGCAA | 11060 |
rs140797145 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69875250 | TTATGTCTAAAAAAT[G/T]TATACACTTTAATTA | 11060 |
rs140799694 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837409 | TCTCAAGGTGTTGTA[A/T]GATGGCTTCTGAGCC | 11060 |
rs140801960 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69812240 | GACATGATCTTGGCT[A/C]ACTGCAACCTCTGCC | 11060 |
rs140802474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904273 | CCAAATCCCCACAGA[C/T]GAAACACCAGCCTCT | 11060 |
rs140816560 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69844354 | TTCACTCTTTTAGAG[A/G]GGAAGGAATACTTGA | 11060 |
rs140832427 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69907421 | AAAGCAAGCATTACC[A/G]CAGAACTGACTGTAG | 11060 |
rs140866730 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69900366 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 11060 |
rs140880900 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841282 | CAGTGAAAACCACAG[C/G/T]GTGCTATGAGATTCC | 11060 |
rs140922526 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69938493 | GCATGGTGGTGGACA[C/T]CTGTAATCCCAGCTA | 11060 |
rs140933501 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | WWP2 | GRCh38.p7 | 16:69911949 | GTGCACCATGGGGCT[C/T]TGGAAAGCCTCAGCG | 11060 |
rs140940374 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69854114 | CTACTTGAACCAGAT[C/G]TGTATCTGGATTCTA | 11060 |
rs140949896 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762022 | AACCCTACTAAAGGA[A/G]CTCAATTAAGTATTT | 11060 |
rs140980306 | snp | C/G | 3.30715e-05 | 0.00406628 | missense | WWP2 | GRCh38.p7 | 16:69937155 | ACCCGAGGCGTGGAA[C/G]AGCAGACCAAAGCCT | 11060 |
rs140998177 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69807967 | AACAAACAAACAAAA[-/A]CAAAAAACATTCTTA | 11060 |
rs141055587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768565 | CAGTGAGCCGAGATT[A/G]CATCACTGCCCTCTA | 11060 |
rs141078562 | snp | A/G | 0.00119737 | 0.0244387 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888217 | ACAGCAGCTCCCAGC[A/G]GCTGCCCAGGCCCCC | 11060 |
rs141085881 | snp | G/T | 0.00915269 | 0.0671332 | intron-variant | WWP2 | GRCh38.p7 | 16:69868299 | CATTCAGGGTAAGCC[G/T]CTATCATTAGTGGTT | 11060 |
rs141088984 | snp | A/T | 0.030665 | 0.119967 | intron-variant | WWP2 | GRCh38.p7 | 16:69801940 | TTTATTTATTTATTT[A/T]TTTTTCTGAGACGGA | 11060 |
rs141092023 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873678 | AGAAAACTCAGTGGC[-/TTT]TTGTGGAGGAGGGCA | 11060 |
rs141103692 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69794067 | GAACTACAGGCGTGC[A/G]CCACCACGCCCGGCT | 11060 |
rs141119607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899269 | AACTTTAGCACTTTG[A/G]GAGGCTTAGGCAGGC | 11060 |
rs141140324 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69796668 | TTTTTTAAAGGCATG[-/T]AGATTCATGCTCTTA | 11060 |
rs141145715 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69883009 | AATACAAAAATTAGC[C/T]AGGCGTGGTGGCACT | 11060 |
rs141156517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69795501 | ATGTGGAACATTTTC[A/G]TCATCATGGAAGTTC | 11060 |
rs141167657 | snp | A/G | 0.029116 | 0.117091 | intron-variant | WWP2 | GRCh38.p7 | 16:69790394 | ATTCAGTGGAAGTGG[A/G]TCATCATAAAGGTCT | 11060 |
rs141190270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833172 | CCTTTTTAAGCCATC[A/G]GTTTGTCTGAGTCAG | 11060 |
rs141219274 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69935417 | TGGCCGCCAGCTCTC[A/G]CTGTCGGCGGTGTCT | 11060 |
rs141219440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782775 | GTGACATTGTTTGAC[C/T]TTAGCTATGGAAAAT | 11060 |
rs141232300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827349 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 11060 |
rs141237458 | in-del | -/A | 0.323434 | 0.238972 | intron-variant | WWP2 | GRCh38.p7 | 16:69849809 | CTCTTAAAAAAAAAA[-/A]TCATGGAGATTAATT | 11060 |
rs141271449 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69881341 | CCCTCTGTGAGCCTC[A/G]GTTTTGTCTGCAGTG | 11060 |
rs141281427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819151 | TGTCACTGTGACTGC[A/T]GCTGTCACCCATGTC | 11060 |
rs141283344 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | WWP2 | GRCh38.p7 | 16:69780646 | TTTCTAATCTGATGA[C/G]TAGCAAAGAGAGTTG | 11060 |
rs141284019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884117 | ATATTCTTGGAATAT[A/G]CAAGCGTATGTATAT | 11060 |
rs141284075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926914 | CGGGGACTTCTAGTG[C/T]ATTTCAGGCTCTGTA | 11060 |
rs141326857 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69775561 | TATTCTCATGTGTTG[A/T]CTGCTGTTTCCATTA | 11060 |
rs141327083 | in-del | -/CACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883400 | TTCTAAGAATGTGCG[-/CACA]CACACACACACACAC | 11060 |
rs141348088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816388 | GGAGTGCAAGACCAG[C/T]GTGGGCAACATAACG | 11060 |
rs141371236 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940329 | TCGGCGAGGAGACTG[A/G]CCACTGGGGGTGGCT | 11060 |
rs141379530 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872109 | CTTCTTCTCTCTCTG[G/T]CATATTCTGTACAGC | 11060 |
rs141387936 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69783976 | ACATAAGATACAAAG[A/G]CACAAGAATTTAACA | 11060 |
rs141401571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69911660 | AATAAAGAGTGCAAT[C/T]GTGCTTCTTAGAAGT | 11060 |
rs141473659 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69841036 | GTGTTTGGGGTGCTT[C/T]GGTGCTTGGAGAAAA | 11060 |
rs141474673 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69907883 | TGTAAATGAATCTTA[C/T]ATTACAAAAATAAAT | 11060 |
rs141484471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877176 | GAAAAGCTGTTGTTT[A/C]GTGTGGCCAACCCCG | 11060 |
rs141492518 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69788117 | CCTGTAATATCAGCA[C/T]TTTGGGAGGCCAAGG | 11060 |
rs141525341 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | WWP2 | GRCh38.p7 | 16:69824991 | GGCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG | 11060 |
rs141546398 | in-del | -/C | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940753 | CAAGAGTTTCCCAAA[-/C]CAGCCACGCCTCTCA | 11060 |
rs141550691 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773794 | GCTGCCCCAGTTTTT[C/T]ATTTGCATAATTTTC | 11060 |
rs141631106 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | WWP2 | GRCh38.p7 | 16:69830340 | GCCATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGT | 11060 |
rs141633678 | snp | A/G | 0.000197713 | 0.0099407 | missense | WWP2 | GRCh38.p7 | 16:69840225 | ACGGGCCAACTGTTG[A/G]TCTGGGAAATGTGCC | 11060 |
rs141637747 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69767596 | ACACGTTGCAAGAAA[A/G]CAATGGGCAGCACAG | 11060 |
rs141664263 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865850 | CTGGCCAGAACCACA[C/T]CATAGTCAGTGGCCT | 11060 |
rs141687177 | snp | G/T | 0.00279664 | 0.0372894 | intron-variant | WWP2 | GRCh38.p7 | 16:69803584 | TTCCACCCTGCTTTT[G/T]TGTGTGTGTGTGTGA | 11060 |
rs141687881 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69815010 | TATTTTTATTTTTTT[-/T]GAGATGGAGTCTCAC | 11060 |
rs141694328 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69867786 | TGGCCTGACTGGCAC[G/T]GCCATTCTAACTGCT | 11060 |
rs141702670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762801 | ATGGCGTGGAGCCAG[A/C]GGGAAAAAGATGCTG | 11060 |
rs141702722 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69801006 | GCCTGGCCAATATGG[C/T]GAAACCCTGTTTCTA | 11060 |
rs141740816 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | WWP2 | GRCh38.p7 | 16:69770066 | GGGATTTCGCCGTGT[C/T]GGCCAGGCTGGTCTC | 11060 |
rs141741162 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69900989 | TTAGATTTAAAGGCT[A/G]GTTCCTTATTTCAGG | 11060 |
rs141746704 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | WWP2 | GRCh38.p7 | 16:69866384 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 11060 |
rs141753291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798983 | GGTGTTCCTACACCA[C/T]TGAGCTCATAGAGCG | 11060 |
rs141758388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864990 | TCCCGAAGAACTTAT[C/G]ATGTTGAGCATCTTT | 11060 |
rs141759371 | snp | A/G | 0.000280008 | 0.011829 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931200 | CAGTTTTCGGTGGAA[A/G]TATCACCAGTTCCGT | 11060 |
rs141764486 | in-del | -/T/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928360 | CCCCCTAGTTTTTTG[-/T/TT]TTTTTTTTTTCTCCT | 11060 |
rs141767645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69869262 | CACATTGAGTATTTC[C/T]ACAGTTCAGTCGTAC | 11060 |
rs141773872 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69805253 | TAAGGCCAGGCTGGT[C/G]TCAAACTCCTGACCT | 11060 |
rs141787503 | in-del | -/GTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845257 | GGAAGTGGCAGTGGG[-/GTTTTTTT]TTTTCTTTGTATCTG | 11060 |
rs141794731 | snp | A/G | 0.00125123 | 0.024981 | missense | WWP2 | GRCh38.p7 | 16:69908784 | AGCGAGAGCTGCCCA[A/G]CGGACGTGTCTATTA | 11060 |
rs141797416 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817691 | TTTTTTTTTTAAAGA[A/G]ATGGAGTCTCGCTCC | 11060 |
rs141803999 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69901648 | GAGAGAGTGGATTTT[A/G]ATTGAGTTAGCTTTA | 11060 |
rs141806606 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69897698 | GTGGATCACAAGGTC[A/G]GGAGTTCGAGACCAG | 11060 |
rs141810056 | in-del | -/C | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69881219 | CTCCCATTTGGGAAA[-/C]ATCAAAGCTGTCTTC | 11060 |
rs141812307 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69816795 | CATATACACACACAC[A/G]TATATACACACATGC | 11060 |
rs141830296 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69896493 | TTCCCTGTACCCAGC[A/G]TACAACTTGGCTTCC | 11060 |
rs141897494 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69891826 | GCTAGAACCTGGTCC[C/G]CCTCCTGGGAATGGT | 11060 |
rs141903250 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69906575 | TCCTAAAAGTCAGCA[C/T]GTGATGCAAAATTAT | 11060 |
rs141908405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69846903 | TTATTCTTCTTTAAA[C/T]GAAATATATATTTAG | 11060 |
rs141948052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857870 | GTGTCTTCCTGTGTT[A/G]CCTAGTCTGGTCTTG | 11060 |
rs141952301 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69792322 | CTGGCATCTGCTCTC[A/G]CAATAAGTTCCAAAC | 11060 |
rs141968687 | in-del | -/ACA/ACAACAACA/ACAACAACAACA/ACAACAACAACAACA/ACAACAACAACAACAACA/ACAACAACAACAACAACAACA | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69783780 | TGAGACCTTGTTTCT[lengthTooLong]ACAACAACAACAACA | 11060 |
rs142012831 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69817298 | CTGTCACCCAAGCTG[C/G]AGTGCAGTGGTGCGA | 11060 |
rs142028468 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804404 | TCTAATTCATTTTTT[-/T]CCCTAATATGTAGCT | 11060 |
rs142066632 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69912220 | TTTGAACCCCAGCGG[C/T]GGAGGTTACAGTGAG | 11060 |
rs142076907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69854613 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 11060 |
rs142079872 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | WWP2 | GRCh38.p7 | 16:69813302 | TGAGTAGCTGGGATT[A/G]CAGGCATGTGCCACC | 11060 |
rs142132991 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789687 | GAATACCCTTCTAGC[A/G]ATGTGCGAGAGTGCC | 11060 |
rs142162579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886820 | CAATGATGGGATGAT[C/T]CTATAGTGAGCTCCC | 11060 |
rs142165244 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69826477 | CTTGGGAGGCTGAGA[C/T]AGGAGAATTGGCTGA | 11060 |
rs142180467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848750 | AGAATGCATGTGAAC[A/G]CACATGAGAGAGTGT | 11060 |
rs142188648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69783713 | CACTTTGGGAGGCTG[C/T]GGCAGAAGAATAGCT | 11060 |
rs142195316 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69926375 | CAGCAGAAGACGGTA[A/G]ACGTTGGTTTGGTGG | 11060 |
rs142269870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69831322 | GGGTGGGGAGGGACA[A/G]TAATGAGAAAATACC | 11060 |
rs142275032 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69766796 | TGTTGTTCTGTTGCC[C/G]AGGCTGGAGTGCAAT | 11060 |
rs142295998 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807645 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAGGAAA | 11060 |
rs142303521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867606 | CCTCATCTGTGTCAG[A/T]ACCACTTTGGGGAGC | 11060 |
rs142308153 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69878978 | TTTATTTTTTCTGCA[G/T]CCTTGTAAATATCGG | 11060 |
rs142418591 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69797396 | TGCACAGTCTGGCTT[G/T]TAGCTCCCTGGCTAT | 11060 |
rs142439160 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69807207 | TGCCCGGCTAATTTT[A/G]TATTTTTAGTAGAGA | 11060 |
rs142465753 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69903569 | GTCAGAAGATCGAGA[C/T]CATCCTGGCCAACAT | 11060 |
rs142474500 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69895884 | AGGATTACACTGAGC[A/G]TCTGTGTCTTTCCTC | 11060 |
rs142476980 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | WWP2 | GRCh38.p7 | 16:69818390 | TTTTTTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 11060 |
rs142484812 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69834979 | CCTGTTGAGTCACTA[C/G]AATAGTAGGTGCTCA | 11060 |
rs142485913 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69897284 | ATTTTTATATTTTTT[A/G]TAGAGATGGGGTTTT | 11060 |
rs142496008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836452 | AAGCATGTGGCATCA[A/G]GTTGCCTTGCTTTGC | 11060 |
rs142497958 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69795890 | TGGCCTCAAGTGATC[A/T]GCCTGCCTCGGCCTC | 11060 |
rs142513531 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888097 | CGTTGTTGGTGTGAC[A/G]TCCCCACCTGCTGCA | 11060 |
rs142551098 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940042 | GAGGCCCCCGTGGAT[A/G]TGGCCCTGTGTGGGA | 11060 |
rs142552168 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69832457 | TACCTAGAAAACTCA[A/G]TGGTAATCATTTAAT | 11060 |
rs142559113 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69894200 | CCTGCCTCGGCCTCC[C/T]GAGTAGCTGGGACTA | 11060 |
rs142563189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69833532 | TGGGGACTTCCCAGA[A/G]TCTTTTCCCTAGATT | 11060 |
rs142572773 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69907194 | AACTCCAGATGTTGA[C/T]GGTGTAGCCTATTAA | 11060 |
rs142600495 | snp | C/T | 0.000286893 | 0.0119735 | intron-variant | WWP2 | GRCh38.p7 | 16:69933925 | CTGTGCAGATGTGCA[C/T]GAAGGGACCCATTAT | 11060 |
rs142614858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69860211 | TTCTTTAAAGGAGTC[A/G]GGGAGGTGATGAGTG | 11060 |
rs142617495 | snp | C/T | 8.25403e-05 | 0.00642365 | missense | WWP2 | GRCh38.p7 | 16:69787032 | TCTGCCAGCTCTAGC[C/T]GGGCAGGAGTGGCCC | 11060 |
rs142625294 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69936087 | CTGCCAGTGTGGCCC[C/G]TGAGCTCTTTTCCAG | 11060 |
rs142657088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928730 | GCCAGGACAACATAG[C/T]GAGACCCTGTCTTTA | 11060 |
rs142664439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865643 | TTACATATTTATCAG[G/T]TTATAGGAGAAGCTA | 11060 |
rs142684933 | in-del | -/TGTTCA | 0.490343 | 0.0688145 | intron-variant | WWP2 | GRCh38.p7 | 16:69852672 | TTTTAAAAATCTGGT[-/TGTTCA]TGTTCTTATTGTTGA | 11060 |
rs142692434 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922334 | GCTGTATTTGCTAGA[C/T]ATTCTTTATTTCTGA | 11060 |
rs142699195 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP2 | GRCh38.p7 | 16:69862110 | CGCTCTTGTTGCCCC[A/G]GCTGGAGTGCAATGG | 11060 |
rs142731614 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761637 | ACCTACCTGGATTAT[A/G]ATTCATTAAGTTCTC | 11060 |
rs142732281 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69859268 | ATATCAAAGGTCATT[C/T]AGGGCTGGGCACAGT | 11060 |
rs142788825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863916 | TTTTATGCATTGAGT[G/T]TATTCCACTATGTGT | 11060 |
rs142797294 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69797270 | AATGTAGATGACTAA[C/T]GACACATGGCAAAAA | 11060 |
rs142800550 | in-del | -/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822533 | CCTGGCCTGGGTGGG[-/GT]GTGTGTGTGTGTGTG | 11060 |
rs142813668 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69777435 | CCTCCTTATTAACTG[G/T]GATTACAGGCACCTG | 11060 |
rs142835843 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69784430 | ATGACATTAACACTT[C/T]GCCTTTTCACTGTGA | 11060 |
rs142844515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69895425 | CTCTGTTCAATGAGA[C/T]GAATCTATTGAGCAC | 11060 |
rs142855973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810266 | CACGTCCCGCAGTGG[C/T]GGATGGTCAACCTGG | 11060 |
rs142863308 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69876468 | CTCCCGGGTTCAAGT[A/G]ATTCTTGTGCCTCAG | 11060 |
rs142867697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69812647 | GCCCAGCTAATTTTT[A/G]AAAATTATTTGGCAG | 11060 |
rs142887057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882652 | TGGGCCGCAGGGGTC[A/G]GGAGGGCGTCCAGGG | 11060 |
rs142897563 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69782019 | CGGGCGAGGTGGCTC[A/T]TGCCTGTAATCCCAG | 11060 |
rs142897655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69821073 | ATCGAGTTGCAGTTA[C/T]ATCAGCGACTACTGT | 11060 |
rs142922639 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69801301 | CAGTGGTGCAATCTC[A/G]GCTCACCGTAGCCTC | 11060 |
rs142937445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809002 | TTACTGTGCTCTGAT[A/C]GTTTGTAATTACTGT | 11060 |
rs142950051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69879884 | CTGTGAGTATTGCAG[A/G]AAAGGATTTAAGAAT | 11060 |
rs142951422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69898878 | CCAGATACTTTTTCT[A/G]TATTTAGTAGAGACG | 11060 |
rs142955243 | snp | A/G/T | 0.016246 | 0.0887035 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838486 | ATAATCAACACTTAC[A/G/T]ATTGCATAGTTTCAG | 11060 |
rs142955840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918064 | TTCCAGTGTGCCTCA[C/T]TCAGCAGCTCCATAT | 11060 |
rs142960097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817630 | TTCTATTGTTTTTTA[C/T]AATTACTAGCAGCAC | 11060 |
rs142996645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784971 | TCGAGTGCAGTGGTT[C/T]ACACCTGTAATCCCA | 11060 |
rs142998180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69906282 | TTTTACTGTGTTAGC[C/T]AGGATGATCTTGATC | 11060 |
rs143019601 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69833016 | ACGCCACCACGTCCA[A/G]CTAATTATTTTATTT | 11060 |
rs143021544 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912582 | TTTTGTTTGTTTGTT[G/T]GTTTGTTTTTGCTGG | 11060 |
rs143050571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934525 | ACTGAACATTAAATA[C/T]GTGCTCTGTTGAGGG | 11060 |
rs143057455 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69844601 | ATCCTGTTAAACCTC[A/G]TTTGTTGTCATTGGT | 11060 |
rs143060753 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | WWP2 | GRCh38.p7 | 16:69780177 | TAAACGTTTGTGTGT[A/C]CACAACAACAACGTA | 11060 |
rs143069370 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69902566 | TTCCTGAGAGCATCA[A/G]CGGAAGCTATCGAGG | 11060 |
rs143077444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69842632 | ATGGCCTCCACTCTC[C/T]GGCTATATTCATGTC | 11060 |
rs143156114 | snp | C/T | 0.00204804 | 0.0319347 | missense | WWP2 | GRCh38.p7 | 16:69871818 | GGACGCACAGACATT[C/T]GGGTGCTTCAGCCAG | 11060 |
rs143185667 | in-del | -/AAAT | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761121 | CTGTCTCAAGCAAGC[-/AAAT]AAATAAATAAATAAA | 11060 |
rs143191483 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905395 | GATCTGAGCAGAAGA[C/T]TGTGATTAAAATGGA | 11060 |
rs143194695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69882010 | ATTTTTGTATAGATG[A/G]GGTTTTGCCATGTTG | 11060 |
rs143199505 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69820253 | TTTTTTGTTATTATT[A/G]TTTTTTTGAGATGGA | 11060 |
rs143212662 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904405 | TTTGAGTTGGGGTCT[A/G]TTGCCTAGGCTGGAG | 11060 |
rs143225042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915380 | TCCCTCATCTTTGGT[A/C]GTGGAAAGTCCATAA | 11060 |
rs143284077 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69861990 | ACCCGGATTGGAATG[G/T]GAGAGGAGTTTTATT | 11060 |
rs143301970 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | WWP2 | GRCh38.p7 | 16:69824926 | CAGGCATGCACAACC[A/G]TGCCTGACTAATTTT | 11060 |
rs143303340 | snp | A/G/T | 0.000115458 | 0.00759717 | missense | WWP2 | GRCh38.p7 | 16:69798721 | ATAATCGTCAACCTC[A/G/T]AATTAACTCCTACGT | 11060 |
rs143311481 | in-del | -/AC | 0.147991 | 0.228242 | intron-variant | WWP2 | GRCh38.p7 | 16:69889146 | AGTGATATCCTGCCT[-/AC]ACACACACACACACA | 11060 |
rs143315818 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69765460 | TTATTAGAGAAGGGC[A/T]CATTGATAACTAAGT | 11060 |
rs143330410 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69921362 | TACTAGACTAGCTAG[A/C]GGCCTCCCCTCCTCC | 11060 |
rs143334739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861349 | AAGTCACCATTTACT[A/G]TACCTTCTCTCTCAA | 11060 |
rs143342771 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69772216 | TCCGCCTGCCTCGGC[A/C]TCCCAAAGTGCTGGA | 11060 |
rs143353944 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69858530 | CCCTTTATCACAGCC[G/T]CCTTGTGCTTGCAAG | 11060 |
rs143354391 | snp | A/G | 4.94205e-05 | 0.0049707 | missense | WWP2 | GRCh38.p7 | 16:69840176 | GAGAACAAAGGCAGC[A/G]TTGTCTCAGGCGGAG | 11060 |
rs143359991 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69793006 | TTAAACCGAATCTAA[C/T]CATGAGGAAACAATT | 11060 |
rs143383701 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761135 | CAAATAAATAAATAA[A/G]TAAATAAATAAATAA | 11060 |
rs143411813 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69888744 | GAGTCTTAATCTGTC[A/G]CCCAGGCTGGAGTGC | 11060 |
rs143436992 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69865664 | GGAGAAGCTATAAAT[A/G]TTTATGAAGGGGACA | 11060 |
rs143441642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863589 | GAGGTTGTAGTGAGC[C/T]GAGATTGCGCCACTT | 11060 |
rs143451530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69796649 | GCACCATTTGTAGTC[C/T]CTATTTTTTAAAGGC | 11060 |
rs143470742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897008 | AATATTGTAAGCATG[C/G]AGATACAAATGGAGA | 11060 |
rs143478209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812139 | CATGACATTGGCATC[A/G]GCGTTGTTGAAGAGT | 11060 |
rs143505435 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69894666 | GGCTAGTGAGATAGT[A/G]GTTCAGGCCGTGGGC | 11060 |
rs143507264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69860698 | CCTGCCTTGTGATTT[A/G]TCGTGTCAGAACACT | 11060 |
rs143518671 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69794106 | TACTTGTAGTAGAGA[C/T]GGGGTTTCACCAAGT | 11060 |
rs143532972 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832353 | TTTATGAAAATCCCG[-/A]ACATACTTCAACTAT | 11060 |
rs143570575 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69890860 | CCTCATCCTGCCAGA[G/T]GCTGAAACACGTTTC | 11060 |
rs143576171 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69841857 | CGGATCCATATGATC[A/G]TCCCTGTTCCTCTTC | 11060 |
rs143613565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69852851 | TACTCATTTATTTTC[A/G]TATTGTCTGTGGCTA | 11060 |
rs143617856 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69786430 | AGGCATGAGCCACTG[C/T]GCCCAGCCAATCTTT | 11060 |
rs143648526 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69884079 | CAAGGCCCACTGTTG[C/T]GTTTCTTGCGGTTCT | 11060 |
rs143703938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845755 | GCCTCTTCTTCAAGA[A/G]TAATCAGATGAAGCC | 11060 |
rs143713702 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WWP2 | GRCh38.p7 | 16:69781372 | TGTTTTTCAAACAGG[A/G]TCTCACTGTGTCACC | 11060 |
rs143723473 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69791400 | ACCCGGCTAATTTTC[A/G]TATTTTTAGTAGAGA | 11060 |
rs143752055 | snp | A/C/T | 4.94173e-05 | 0.00497053 | missense | WWP2 | GRCh38.p7 | 16:69888096 | CCGTTGTTGGTGTGA[A/C/T]GTCCCCACCTGCTGC | 11060 |
rs143758674 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69828470 | CTCCCTAGTTCAAGC[A/G]AGTCTCCTGCCTCAG | 11060 |
rs143830543 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69876943 | TTTGTTGCTCCATTT[A/G]TAAAACACAAGCAGA | 11060 |
rs143857846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918742 | CCTGTTCCCCTCAGA[A/G]CAGTCTTCAAACGTT | 11060 |
rs143865442 | snp | C/T | 0.00034587 | 0.0131459 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934045 | TGCCGGAAAGAACAA[C/T]TACTGCCTGCAGATC | 11060 |
rs143892519 | snp | A/G | 0.109461 | 0.206758 | intron-variant | WWP2 | GRCh38.p7 | 16:69872298 | CTCGGCTCACTGCAA[A/G]CTCCGCCTCCCGGGT | 11060 |
rs143928366 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69880243 | ATTGTCACAAAGACA[G/T]TAAGTAAACAGTGTC | 11060 |
rs143936724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69779295 | TTGGAAAGGTTTTAC[A/G]ATTCCAAATGCCTAC | 11060 |
rs143957999 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69826352 | GCAGGCAGATCACAA[A/G]GCCAGGAGTACGAGA | 11060 |
rs143963259 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760702 | AGACCCAAAAATAAC[A/G]GATTAGTACAAGTCT | 11060 |
rs143982826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69877800 | TTTATTATTAAATTT[A/G]CTTTTTATTTATTTA | 11060 |
rs143999663 | snp | A/G | 0.00189324 | 0.0307089 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925452 | GTGCTTCGACTGACC[A/G]TGATCCCCTGGGCCC | 11060 |
rs144009683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69862499 | CAGGCAATCCAACCA[C/T]CTCGGCCTTCCAAAG | 11060 |
rs144010110 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942013 | ACCCGGGGGTCTCCA[A/G]GCAGTTGCTGTGGGG | 11060 |
rs144030099 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69775089 | TTTAGGTTTGATGAA[A/C/G]AGTGGACAATCGTGG | 11060 |
rs144070148 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | WWP2 | GRCh38.p7 | 16:69828905 | CTTCTGAGCTCTCTT[C/G]CCACGTATCTGACGA | 11060 |
rs144078365 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69763990 | CACTTCATGATTACT[C/T]TCCCATTTACAAAGA | 11060 |
rs144099282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793642 | CACGAGTCAAGTCAC[A/G]GGCCCAGGCAAAGTC | 11060 |
rs144139434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69825827 | ACACAGGATCTCCCT[A/G]TGTTGCCCAGGCTGG | 11060 |
rs144173843 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856786 | TCAAAAATAAAAAAT[-/A]AAAAAAAAAATACAA | 11060 |
rs144194905 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918137 | TTCCCCGTCTTTCTT[-/C]CGAGATCGGCTTTCA | 11060 |
rs144202729 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69823118 | CCTGCGCAACAGAGC[A/G]AGACTGTGTCTCAAA | 11060 |
rs144217325 | snp | C/T | 0.031825 | 0.122064 | intron-variant | WWP2 | GRCh38.p7 | 16:69866998 | ATGCGCCACCAGGCC[C/T]GGCTAATTTTTGTTT | 11060 |
rs144260449 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812971 | CTAGTTTCTGCATCC[A/G]GTGATTTTACTCTGA | 11060 |
rs144269070 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69818737 | TCCATCTCTCTGGTC[A/C/G]CTCTCATTCAGTCTC | 11060 |
rs144287207 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908921 | AATGGCTTCTTGAAA[C/T]GGTCCCTTTCTGCGG | 11060 |
rs144330002 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914187 | TTTAGCAAGAACTTG[C/T]GGAATAGCAGGAAAG | 11060 |
rs144332207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69856087 | GTCTAGCCTGGGCAG[C/T]ATAACAAGACTCCCA | 11060 |
rs144364104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69818132 | ACCTTAGTCTGTTAG[A/G]CAAAGTGATTTCTCT | 11060 |
rs144393729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69911152 | AGACCTAGTCCCTGG[A/G]GAGCAAGATTGAACC | 11060 |
rs144399556 | in-del | -/AGTC | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69793672 | AGTAGATTGCCAGAA[-/AGTC]AGAAAAAATCTCAAA | 11060 |
rs144402100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69851496 | TTACGTTTCTTTCAC[A/G]TCTTCTCATGGCTTG | 11060 |
rs144405595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764355 | ACAGGTGGGTGCCAC[C/T]TCGCCTGGCTAATTT | 11060 |
rs144460842 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69877358 | CTCACCACTCTCAGC[C/G]TTCATAGAATTGAAG | 11060 |
rs144473170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813891 | CAACATAATCCAATA[C/T]AGGTAAAATTTACTA | 11060 |
rs144499959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69859617 | ATTTAGTTATTTGCA[A/G]TTGTAGGACTGAGGT | 11060 |
rs144503914 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69793362 | ATCTAAAAAAATAAT[A/G]ATAATAAATAAATAA | 11060 |
rs144534264 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889834 | TGTATCCTGTGAACC[A/G]TTGTGATTCATAAAG | 11060 |
rs144539224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811051 | TGAGCCACCATGCCC[A/G]GCTGGAATTTTCAAA | 11060 |
rs144540676 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69803800 | GTAATCCCAGCTACT[C/T]AGGAGTCTGAGGCCG | 11060 |
rs144597253 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69870580 | TGTTAGGATAACAGG[C/T]GTGAGCCACTGTGCC | 11060 |
rs144601943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69807477 | TAAAAAAATTAGCTA[A/G]GTGTGGTGGTGTGTG | 11060 |
rs144622117 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69806938 | CCCTAGATCTGTTTT[A/T]TTTATTTATTTATTT | 11060 |
rs144635303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802695 | AACCCCTGTCTCCTG[A/G]GTTCAAGTGATTCTC | 11060 |
rs144666460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834021 | GCTCTTGCCTGGATT[A/G]CCACAGTGACCTCCT | 11060 |
rs144693307 | snp | C/T | 4.9543e-05 | 0.00497685 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937187 | CCTGGATGGCTTCAA[C/T]GAGGTGGCCCCGCTG | 11060 |
rs144705247 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69846564 | CTTCTCTACTAAAAA[C/T]ATAAAAATTAGCTTG | 11060 |
rs144708327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781960 | ATCCAATCACCTCTT[C/T]AAGGCCCCACCTCTC | 11060 |
rs144745923 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69898219 | TTTTAGTAGAGACAG[G/T]GTTTCGCCATGTTAG | 11060 |
rs144747099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69897517 | CTGTATACAGTGATA[C/T]ATGGAACTTGGGACA | 11060 |
rs144750221 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837572 | GCAGTGTGACTGTCA[C/T]GGGGGTAGAAATTAG | 11060 |
rs144802638 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941688 | TGTTTTGTAATGCCC[A/G]CCCCTTGCCTCGATA | 11060 |
rs144809409 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941644 | TCTGTACGGAATGCC[C/T]TTTGCTAGCCATGGG | 11060 |
rs144809496 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69896368 | TCAAGCGATCCTCCT[A/T]TCTTGGCCTACCAAA | 11060 |
rs144814000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784590 | GGTTCGCCTGAGAAT[A/G]TCCTTGATGAAGTGG | 11060 |
rs144814265 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940131 | CCCGACCCGCGGATG[A/G]CAGTCTGGAATAAAG | 11060 |
rs144843054 | snp | A/G | 0.000264651 | 0.0115002 | missense | WWP2 | GRCh38.p7 | 16:69937584 | GAGATAGACATGAGC[A/G]ACTGGCAGAAGAGCA | 11060 |
rs144844646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69882875 | TTAATACAGCAGACC[A/G]GGTGCGGTGGCTCAT | 11060 |
rs144846888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822407 | CTCCTGGAATTTAGA[C/T]TCTAGAGAGGAAAAC | 11060 |
rs144873934 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69938534 | TGATGCATGAGAATC[A/C]CTTGAACCTGGGAGG | 11060 |
rs144881506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69779825 | CCCCAAGGCTCAATT[C/T]ATAATTATTTATAAT | 11060 |
rs144932234 | snp | A/T | 1.65127e-05 | 0.00287334 | missense | WWP2 | GRCh38.p7 | 16:69930254 | CGCCCGGGGTTTGAG[A/T]CGGGGTAAGGACTTT | 11060 |
rs144946190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910862 | GAGGTGGGACACTAC[C/T]AATCAAGCTGTCTTA | 11060 |
rs144969374 | in-del | -/AAATGGG | 0.0441095 | 0.141807 | intron-variant | WWP2 | GRCh38.p7 | 16:69817142 | TGCCTTTTTCCCCCC[-/AAATGGG]AACTCATTATACATA | 11060 |
rs144977360 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69857287 | TTTTAGTAGAGATGG[A/G]GTTTCACCTGTTGGC | 11060 |
rs144981817 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | WWP2 | GRCh38.p7 | 16:69790652 | GTGATCTTGGCTCAC[C/T]GCGACCTCTGTCTCC | 11060 |
rs145027707 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69855541 | TGAGTTTGATTCATG[C/G]GAAAAATATGTATAA | 11060 |
rs145028606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819578 | TCTTCATTTTAATTT[A/G]ATTTAATTTTCTAGA | 11060 |
rs145029934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69854512 | ATGACTCCTTTCAAA[C/T]GTTGAATCAATTCTG | 11060 |
rs145033404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69787668 | TTGCTACCTGCACTC[C/G]CTCCCTAGGTGCTTC | 11060 |
rs145063659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884127 | AATATACAAGCGTAT[A/G]TATATATATTCCTTG | 11060 |
rs145081584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69914855 | GCATCTTCAGACATT[C/G]TGGGCTTCAAAAAAT | 11060 |
rs145093867 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69857019 | ATGTTTCTCGTGATT[C/G]TTGATATCTTTAGAG | 11060 |
rs145096588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69882707 | ATGCAGCAAGAACAC[A/G]AGGGACAGAGAGTGG | 11060 |
rs145100936 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69785493 | AGAACTCAATGAACC[A/G]ATATTTTTCAAATGT | 11060 |
rs145110293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69766214 | GAGTCACCCTTGACT[C/T]GTCTCTTCCTCTCAC | 11060 |
rs145156318 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69883667 | TGCACAGATCAACCC[A/G]TCACCTAGGTATTAA | 11060 |
rs145175944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799990 | GGCATGGAAAGAAAG[A/G]CTCCTTTTTCTCTTG | 11060 |
rs145217171 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WWP2 | GRCh38.p7 | 16:69919655 | TCTTTGGTAGGGAGA[C/T]GTGGGACTCCCAAGT | 11060 |
rs145221206 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69881726 | AGATAGAGCCTCACT[C/G]TGTCACCCAGGCTGG | 11060 |
rs145232831 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69819418 | CTTTCCAGATCCCTC[A/G]GGCCACAGGTCTCCC | 11060 |
rs145236505 | in-del | -/GA | 0.104859 | 0.203554 | intron-variant | WWP2 | GRCh38.p7 | 16:69877746 | AATGTAGGGTATAAG[-/GA]GAGAGAGAGAGAGAG | 11060 |
rs145238845 | in-del | -/AGTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771949 | ACTAAAAGTCTTTTT[-/AGTC]TTTTTTTTTTTTTTT | 11060 |
rs145241384 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69777051 | TATGTGTGTGTGTGT[A/G]TATATATGTATGTAT | 11060 |
rs145268330 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WWP2 | GRCh38.p7 | 16:69914538 | CAAGGCAGGAGGATC[A/G]TTTGAGTCCAGGAGT | 11060 |
rs145289296 | in-del | -/TT | 0.319376 | 0.240181 | intron-variant | WWP2 | GRCh38.p7 | 16:69854541 | TTTCTTTTTTTTTTT[-/TT]AAGTTTATTTATTTT | 11060 |
rs145297269 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69874680 | ACTTGTATGGGATGA[G/T]TTACTTGCTAATTCT | 11060 |
rs145297356 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69836054 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs145307692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774152 | TTTAACCTAACTCTA[C/T]ACATTCAATTACATC | 11060 |
rs145327694 | snp | C/T | | | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888115 | CCCACCTGCTGCACC[C/T]TTGAGTGTGACCCCG | 11060 |
rs145348986 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837080 | AGTTGCCTACTACCA[G/T]ATCCAGCTAATTTTT | 11060 |
rs145354295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775999 | GTTTTCCCTAAAAAC[C/T]CCTTCTTAAATAGAG | 11060 |
rs145371186 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69903096 | TCGCTAAGCCAGTTG[A/C]GGGGGTTCATAGAAG | 11060 |
rs145373247 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69843950 | ATTTTAGCCAATACC[C/G]GCAGCATCTTAAAAG | 11060 |
rs145412440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834153 | GTCCCATGTTGAGCA[A/G]TTTCCAAGGACCTTG | 11060 |
rs145421784 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69935706 | CTCCTGAGGCCCTCC[C/T]GCTGCGTCCGAGGCA | 11060 |
rs145439688 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69896931 | ACACGTATAACACAC[A/G]TCTACCAAAAGTTGA | 11060 |
rs145460972 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69938109 | GTATTCTTAGTACAT[A/G]TCTGTGTGCATATGT | 11060 |
rs145470126 | snp | C/G/T | 0.00114796 | 0.0239303 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939098 | TACCTGCCGCCTGCC[C/G/T]GTCGGGGGATTTGCC | 11060 |
rs145472785 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69939210 | CTCTTCCTGGAAGCA[C/T]GTCAGTGGGATGGAG | 11060 |
rs145477977 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69869945 | GGAACTTTCTATTAT[A/G]GCTCTTAATTTCACC | 11060 |
rs145478732 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848062 | GGAAATGGAACAACA[A/G]CAACAAAATGAGAAG | 11060 |
rs145484690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782710 | CTTTTTGGAAACTAG[A/G]TATATCACATAAGAC | 11060 |
rs145511360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880807 | CGAGCTGATCTTCAG[C/T]AGAAAGAACTTCTGT | 11060 |
rs145530470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933607 | ATCGTGCCCTTGTGC[A/G]GTGCACAGCCTAGGC | 11060 |
rs145542795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69867817 | TTCTGCCTGCCCTGG[A/G]GGCTGTATAACTCGT | 11060 |
rs145587762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786084 | CTCTACAGCTAGCAC[A/G]CTAGATTAGCTGTCT | 11060 |
rs145603873 | in-del | -/TCAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919129 | ATTACAAGCATGAGC[-/TCAG]CACCATCCCCGACCA | 11060 |
rs145623978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884043 | CTTTTTCCTATTCTG[A/C]TCACCTTCAGTTTCC | 11060 |
rs145628159 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69824119 | TCCGCACCAGTCATT[C/T]GGGCGGCTTCCGCCT | 11060 |
rs145638157 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69797114 | GACCTGGCGTTTCCA[C/T]CAGGGGTAATATACA | 11060 |
rs145646183 | in-del | -/T | 0.0930568 | 0.194599 | intron-variant | WWP2 | GRCh38.p7 | 16:69813462 | CCACTGCGCCCAGCC[-/T]TTTTTTTGTTGTTTT | 11060 |
rs145666924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820901 | ATTACTGAGGATGAA[C/T]GTCTTTTCCTGTGAC | 11060 |
rs145667929 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69861031 | CTGTACAGGTTGTGC[A/T]CTGCATTCCTTGGGG | 11060 |
rs145688800 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69920034 | TCCTGGGCTCAAGCA[A/G]TCCACCTGCCTTGGC | 11060 |
rs145696632 | in-del | -/ATGTATCT | 0.0584853 | 0.160693 | intron-variant | WWP2 | GRCh38.p7 | 16:69878681 | TTTATACATGGTTTC[-/ATGTATCT]ATGTGCTCTTCTTTG | 11060 |
rs145705062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915655 | AAAGTGGTTGCCTTC[G/T]GGGAACAGGAGTCAG | 11060 |
rs145706603 | snp | A/C | 1.65252e-05 | 0.00287443 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937214 | GCTGGAGTGGCTGCG[A/C]TACTTTGACGAGAAA | 11060 |
rs145709330 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69857765 | CTCCCAGGCTCAAGT[A/C/G]ATCTTCCCACCTCAG | 11060 |
rs145746985 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69892266 | TTACATAGGTATACA[C/T]GTGCCATGGTGGTTT | 11060 |
rs145761817 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69828020 | GGGGTACCTTGTTAC[A/G]TGGGTGACTGTAATG | 11060 |
rs145764463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69912221 | TTGAACCCCAGCGGC[A/G]GAGGTTACAGTGAGC | 11060 |
rs145793802 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | WWP2 | GRCh38.p7 | 16:69864953 | TATGTAATGATATCT[C/T]ATTGTAGTTTTAATT | 11060 |
rs145799862 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838370 | CCCCTCTTAATCCAC[A/G]TGCTTAAAAACCCTA | 11060 |
rs145803787 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WWP2 | GRCh38.p7 | 16:69776627 | CTGAGGTCAGGTGTT[C/T]GAGACCAGCCTTAAC | 11060 |
rs145832829 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69872833 | CCCGTAAGTGAGACG[A/G]GAAGGACCTATTTCA | 11060 |
rs145896117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815956 | AGAGTCAGGGTCTTA[C/T]TATGTTGCCCAGGCT | 11060 |
rs145912696 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772750 | TTTTGGTGCCTCTTC[C/T]CTGTTTCAGCCAGTC | 11060 |
rs145934252 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | WWP2 | GRCh38.p7 | 16:69812456 | AGGCATGAGACACCG[C/T]GCCTGCCCCCAACCC | 11060 |
rs145975966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69798609 | TAACTAAAAAGAGCC[A/G]GAACATCTGCCACAG | 11060 |
rs145994314 | snp | C/T | 0.00107733 | 0.0231842 | missense | WWP2 | GRCh38.p7 | 16:69871871 | CAAAGCCCCGGTGCT[C/T]GGAGCCGGCACCGCC | 11060 |
rs145994348 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69836526 | GCCAGAGGTCTCAAA[C/T]AGAACAGAGGAGGGT | 11060 |
rs145994951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796262 | TGTGTATGAGCGCAG[A/C]TACTTCTCAACTTAC | 11060 |
rs146005933 | in-del | -/ATAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778089 | TATATATATATATAT[-/ATAC]ACACACACACACACA | 11060 |
rs146010200 | snp | A/C | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69894222 | CTGGGACTACAGGCG[A/C]ATGCCACTATACCCA | 11060 |
rs146029439 | snp | A/G | 0.00648566 | 0.0565753 | intron-variant | WWP2 | GRCh38.p7 | 16:69936492 | CGCTCCAGGGGTGGC[A/G]TGGAGATCTAGTGGG | 11060 |
rs146031503 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69890252 | ACCTTTACTACGTAC[G/T]TATTGTTTTCCTAGC | 11060 |
rs146052825 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WWP2 | GRCh38.p7 | 16:69907647 | GCAAATAACAGGAGT[A/G]TGGGGATAAGTGGTC | 11060 |
rs146069468 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69848786 | TGTGTGTTTGTGTGT[A/G]CATGTAGGCCTGGGG | 11060 |
rs146095976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69850023 | GGAAGGAAGGCAAAT[C/T]TCTGCCGTTGAAGGC | 11060 |
rs146098653 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69784450 | TTTCACTGTGATCCC[A/G]TTCACACCAATGTTC | 11060 |
rs146134968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69879972 | CAATAATGTAAAAGT[C/T]CTTATCTATAAAATG | 11060 |
rs146165459 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795276 | CACACACACACACAC[A/C]CACACACACACACAC | 11060 |
rs146169739 | in-del | -/AA | 0.0652144 | 0.168387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836836 | CCCAGGATGGTCTCG[-/AA]GAATTCCTGAGCTCA | 11060 |
rs146198717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69845768 | GAATAATCAGATGAA[A/G]CCTGGGCGTGGTGGC | 11060 |
rs146199930 | snp | C/T | 0.00339027 | 0.0410322 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931541 | CCACGTGAAGATCAG[C/T]GTTTCCAGGCAGACG | 11060 |
rs146218751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833219 | ATATATCTTTTCAGT[A/C]TCTCTTAACTTAGAG | 11060 |
rs146220926 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69769834 | CCATTTCCTGGCCTA[G/T]AACTCCTAAAATCAT | 11060 |
rs146237281 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69830766 | GTTGGAAGCCGAAGA[A/G]CCATCGTAACAGTAA | 11060 |
rs146237446 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69869008 | ATTCTCCTGCCTCAG[A/C]CTCTGAAGTAGCTGG | 11060 |
rs146254089 | snp | A/G | 0.0338734 | 0.125655 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931252 | GGTACTGGGGCTCCC[A/G]TGGCAGTTGGGGTTA | 11060 |
rs146255554 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866495 | TAGCTCCTTGCAACC[A/G]TCATCCCGCTTTCTC | 11060 |
rs146272908 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69926519 | GGTTTGGAGCTGGAT[A/C]TTCTCGATGCAGACA | 11060 |
rs146337529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69817333 | GGCTCACTGCAGCTT[C/T]AACCTCCCAGGCTCA | 11060 |
rs146359335 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69813423 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 11060 |
rs146373988 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909203 | CCAAAGGATGAGAGA[A/G]GCTTCCAAGAGAGGG | 11060 |
rs146392449 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69906740 | AAAAGATTAGCTGGG[A/C]CTCGTGGCATGCACT | 11060 |
rs146414353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844243 | ATGACAGTGTAACTG[A/G]CAAATCTTGTGTCAA | 11060 |
rs146429535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69900185 | TAAGGGCCATTCACA[A/G]GAAAAATAATTAAAC | 11060 |
rs146448854 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942072 | TGGGCTTCCGAAACT[A/G]GCTTGCAGGGAGAGT | 11060 |
rs146490262 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | WWP2 | GRCh38.p7 | 16:69818309 | GCCTCCCGGGTTCAA[A/G]CAATTCTCCTGCCTC | 11060 |
rs146499967 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69793973 | ACCCAGGCTGGAGTG[C/T]GTTGGACAATCTCAG | 11060 |
rs146519420 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830960 | TTCCTCTGTGTACCA[A/G]TGTTTGCAGTTATGT | 11060 |
rs146520135 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69790120 | GGCGTGGTGGCAGGC[A/G]CATGTAATCCCAGCT | 11060 |
rs146537494 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69887499 | CAAACTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 11060 |
rs146555111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926845 | AGGCAGGGGAAAATG[C/T]GTCAGATTAAACAAG | 11060 |
rs146555975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69884082 | GGCCCACTGTTGTGT[C/T]TCTTGCGGTTCTTTC | 11060 |
rs146574979 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69920432 | CTTTCACCACATTTC[A/G]GAGATTGCTCCTTTT | 11060 |
rs146616060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797460 | TGTTTTCTCCTGGGT[A/G]AAATGGGGTGATGAT | 11060 |
rs146620816 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69778986 | ATGGAGTCTCGCTCT[G/T]TTGCCCAGGCTGGAG | 11060 |
rs146625666 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | WWP2 | GRCh38.p7 | 16:69881881 | TATTTTTAGTAGAGA[A/C]AGAGTTTTGCCATGT | 11060 |
rs146639151 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | WWP2 | GRCh38.p7 | 16:69814134 | GAAAATAAAGTCAGG[C/T]ACCTTGCATACCAAA | 11060 |
rs146655334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874552 | CACAACCATAAAGTA[C/T]CCATTTTTATAAAAC | 11060 |
rs146657296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811331 | ATAATTTCAGGCTAG[A/G]TGTGGTGGCTCACAC | 11060 |
rs146659547 | snp | C/T | 4.94597e-05 | 0.00497266 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69798734 | TCGAATTAACTCCTA[C/T]GTGGAGGTGGCGGTG | 11060 |
rs146691611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69904692 | TGCATTTTCATCTGG[C/T]CACTTTTGCCAGATC | 11060 |
rs146738158 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | WWP2 | GRCh38.p7 | 16:69826505 | TGAACCCAGGAGGCA[C/G]AGGTTGCAGTAAGCC | 11060 |
rs146749657 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69794994 | CTCTGGCGGGTAGAT[A/C/T]GCTTGAGTCCAGGTG | 11060 |
rs146774694 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69864108 | GTGGCTCATGCCTGT[-/A]ATCCCAGCACTTTGT | 11060 |
rs146776585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860730 | AGAAATAATGCTCTA[A/C]CCAGCTCATGCCTCT | 11060 |
rs146795561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857509 | AATTCTGCATCCAGT[G/T]GTGTGAAGAGAGCAA | 11060 |
rs146812327 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827689 | AACTGAGAGAGGCGG[-/TT]GTGGCCGCTGCGGTT | 11060 |
rs146812896 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887840 | ATTTATTTCGGATTC[A/T]TCCTGATTTCCTTTG | 11060 |
rs146860803 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69810864 | GGTTCAGGCAATTCT[C/G]CTGCCTCAGTCTCCT | 11060 |
rs146880494 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69807303 | GTCTCCCATACTGCC[G/T]GGATTACAGGCGTGA | 11060 |
rs146906348 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69888303 | CAAAGACTGAGGCTC[C/T]TTTACGGGGGTGGAA | 11060 |
rs146906485 | snp | A/G | 0.000387261 | 0.0139097 | intron-variant | WWP2 | GRCh38.p7 | 16:69933926 | TGTGCAGATGTGCAC[A/G]AAGGGACCCATTATT | 11060 |
rs146909845 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69829274 | CTTCCTTTCCTCCGG[C/T]TTGTTTTCCACACCA | 11060 |
rs146922906 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69929260 | CCCACCACCAACAAG[A/G]AAGGACCCTCTTTGT | 11060 |
rs146965724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782871 | AGCCAAGGTCTCACT[A/G]TGTTGCCCAGGCTGG | 11060 |
rs146982594 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69780914 | ATGCCTGTAGTCCCA[A/G]CTACTCAGGAATCTG | 11060 |
rs146999337 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69816413 | ATAACGAGACCCACC[A/G]CTCTATTAAAAAAAA | 11060 |
rs147012529 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69911819 | AGGGATGGAAGAGGA[A/G]AAACAGCATATGGGA | 11060 |
rs147015587 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69812731 | GCATTCTTGGCAGGA[A/C]CACCCAGGAGTGACT | 11060 |
rs147030663 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69908341 | CTTGTGGAGGGGTCT[A/G]TGAAACCCAGAAATT | 11060 |
rs147051324 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69908824 | CAATACCAAGACCAC[C/T]ACCTGGGAGCGGCCC | 11060 |
rs147069468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69832122 | GTGTGAGCCACTGCG[C/T]CCTGCCTTCTTTGTT | 11060 |
rs147071430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767683 | TGCTGGAGGGGGCTA[G/T]GTGGGGATTGATGCA | 11060 |
rs147074353 | snp | C/G | 0.00147335 | 0.0271017 | missense | WWP2 | GRCh38.p7 | 16:69842059 | GACTCCAGTGGAACA[C/G]CAGTAGCTCCAGAGA | 11060 |
rs147075563 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817794 | CTTCCGAGTAGCTGA[A/G]ATTACAGGCTTGTGT | 11060 |
rs147087762 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69763592 | AATTAGTTTTTGCAG[C/T]AGCGCCTATGAGTGA | 11060 |
rs147088835 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | WWP2 | GRCh38.p7 | 16:69823599 | CAGCCTCCCAAGTAG[C/T]TGGGATTACAGGTGT | 11060 |
rs147101522 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69865072 | AATCTTTTTTTTAGT[C/T]GGGGTTTGGCTCTGT | 11060 |
rs147117683 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69862018 | ATTAGGTAATTTTAC[A/T]TTTTGTGCCTGTTTT | 11060 |
rs147133759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858589 | CACTGCCTGCACAGT[C/G]TCTGTGGCTTCATCT | 11060 |
rs147136892 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | WWP2 | GRCh38.p7 | 16:69793184 | GGTGAAATCCTGTCT[C/G]TACTAAAAATACAAA | 11060 |
rs147147023 | in-del | -/G/GG | 0.040671 | 0.13668 | intron-variant | WWP2 | GRCh38.p7 | 16:69890541 | CTGTATGTTATAATT[-/G/GG]TGGGGGGAACAATGC | 11060 |
rs147152913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69789514 | ATTACGGGCGTGAGC[A/C]ACCGTGCCCAGCCTC | 11060 |
rs147166577 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69886521 | TCCCAGCACTTTGGG[A/G]GGCTGCAGTGGGCAT | 11060 |
rs147206733 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | WWP2 | GRCh38.p7 | 16:69808580 | CTAATTTTTGTATTT[G/T]CAGCAGAGACAGGGT | 11060 |
rs147239821 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69842304 | GATCCTTATTTATTT[A/T]TTTTTTAATTGAATT | 11060 |
rs147256627 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837124 | GAGATGGGGTTTTAC[C/T]ATGTTGCCCAGGCTG | 11060 |
rs147256694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876948 | TGCTCCATTTATAAA[A/G]CACAAGCAGAGTAGA | 11060 |
rs147259282 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69776038 | TTTCAGCCCTAATTC[C/G]CTGTTGTTGTACTGG | 11060 |
rs147273554 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69872418 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 11060 |
rs147314393 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69792740 | TCTGTCACCTAGGCT[A/G]GAGTGCAGTGGCACA | 11060 |
rs147330970 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69788500 | CTTGCTCTTCAGTGA[A/G]TACACTGGGCAGGCG | 11060 |
rs147332645 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | WWP2 | GRCh38.p7 | 16:69927623 | CTGGACAGATCCCCC[-/T]GGCCCTGTGGTTAGC | 11060 |
rs147344610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885988 | TCTCGAAGAGGGCAG[C/T]CAGATGATCGGGAAA | 11060 |
rs147352261 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845911 | AAAAATTAGCCAGGC[-/AT]GGTGGTGTGTGCCTA | 11060 |
rs147364595 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69823363 | TGGCCCCCATATTGG[A/G]CAGTGCAGGTCTAGA | 11060 |
rs147436790 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69775571 | TGTTGTCTGCTGTTT[A/C]CATTAGAGCCCTGAA | 11060 |
rs147451415 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69872247 | TTTGAGACGGAGTCT[C/G]ACCCTGTCGCCCAGG | 11060 |
rs147452807 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69809016 | TCGTTTGTAATTACT[A/C/G]TTGTGATTTTATCTT | 11060 |
rs147467991 | snp | C/T | 0.11228 | 0.208646 | intron-variant | WWP2 | GRCh38.p7 | 16:69906351 | TGCTGGGATTACAGG[C/T]GTCAGCCACCGCACC | 11060 |
rs147469729 | snp | C/T | 0.115088 | 0.210473 | intron-variant | WWP2 | GRCh38.p7 | 16:69806953 | ATTTATTTATTTATT[C/T]ATTCATTCATTCATT | 11060 |
rs147484450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69902603 | GGAGATGACCCATGT[A/G]ACCAAGATGCAGTGT | 11060 |
rs147550587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934262 | GGGGCAGCATTGGAG[G/T]AGGCCCTGGGCCTGT | 11060 |
rs147590302 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69850904 | ACTCTCTTCCCCACT[A/G]TCAACATCCCCCACC | 11060 |
rs147602011 | in-del | -/A | 0.122411 | 0.214991 | intron-variant | WWP2 | GRCh38.p7 | 16:69804081 | TTTTGGTATTGAAAG[-/A]AACTCTTTATTTGTT | 11060 |
rs147606470 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69883814 | TTAGGCCTGTGGACA[C/T]GTACAGCCCTGGAGG | 11060 |
rs147606557 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848343 | TAATCCCGGCTACGT[C/G]GGGAGCTGAGGCAGG | 11060 |
rs147608376 | snp | A/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783063 | TCCCCCAGGCTGGGG[A/T]GCAGCGGCGTGATCT | 11060 |
rs147683911 | snp | A/G | 1.6554e-05 | 0.00287693 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936444 | GGAGAACAAGGAAGA[A/G]TACATCATGTGAGTC | 11060 |
rs147694100 | snp | A/G | 0.000247343 | 0.011118 | missense | WWP2 | GRCh38.p7 | 16:69917800 | CCGACCGCGGAGTAC[A/G]TGCGCAACTATGAGC | 11060 |
rs147694668 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | WWP2 | GRCh38.p7 | 16:69834526 | CATTAAAAAATTTTT[C/T]TTTAGTTTTTTTTTT | 11060 |
rs147697607 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69772108 | CTGGGATTACAGGCA[C/T]GCACCACTACACCTG | 11060 |
rs147708483 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | WWP2 | GRCh38.p7 | 16:69938279 | TCACCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 11060 |
rs147710712 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | WWP2 | GRCh38.p7 | 16:69870000 | ATAGCCCAAGAGGAA[A/T]TTAGCTTGAGTTCAG | 11060 |
rs147712037 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69832242 | AGGTGGAAAAACAGT[C/T]GATGAATCCCCACAT | 11060 |
rs147713739 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69767998 | ATGTGCCACCATGCC[C/T]AGCTAATTTTTAACT | 11060 |
rs147724481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69933729 | GAGCCGACAATCACA[C/T]GTTTTCCCAAATATC | 11060 |
rs147728285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867849 | CCCTCCCCCTAAATG[A/G]TGAGGGGGCTTGGGC | 11060 |
rs147766796 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69785055 | AGCTTGGCCAACATG[A/G]CGAAACCCCATCTCT | 11060 |
rs147799676 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69819052 | CAGGCTAAAATCCTC[A/C]GTGCCTTCCTTGACT | 11060 |
rs147816344 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69856121 | CTAAAAAAGATGTAT[A/G]TTTATTTGGTCTGAC | 11060 |
rs147831584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69911372 | AAGAGGATTGAGGAG[A/G]CCTCACAGAGGGAAG | 11060 |
rs147832593 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69851940 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 11060 |
rs147894462 | snp | C/T | 0.000164736 | 0.0090742 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840211 | GACAATTTTCCTGGA[C/T]GGGCCAACTGTTGAT | 11060 |
rs147903639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867636 | CGTGGGTCCTGGTCG[C/T]GGCTGGCCTGCCTTC | 11060 |
rs147906123 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69800857 | GGCGTGAGCCACTGC[A/G]CCCAGCCTGATAGTT | 11060 |
rs147921462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898332 | CACTCCCAGCCAGTT[A/G]TTTCTTAAAGATTTG | 11060 |
rs147923466 | snp | C/T | 0.123105 | 0.215401 | intron-variant | WWP2 | GRCh38.p7 | 16:69797751 | AAAATTAGCCAGGCA[C/T]GGTGGCGGGCGCCTG | 11060 |
rs147929112 | snp | C/T | 0.000203035 | 0.0100736 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888235 | TGCCCAGGCCCCCGA[C/T]GCTCTGCCTGCTGGG | 11060 |
rs147938353 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69896427 | TGCCCATCCTTACTG[C/T]AATTTCTTGAGAGCT | 11060 |
rs147959080 | snp | A/G | 3.2962e-05 | 0.00405954 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936384 | ACTGGGCAAGGTGAC[A/G]ACCCACGAGCTGAAG | 11060 |
rs147990108 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69798529 | TGGTGTGTGTACTCA[A/C]ATTTCTTTAAAAAGT | 11060 |
rs147992282 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69777099 | ATATGGATATATATA[C/T]ACACATATGTGTATA | 11060 |
rs148005250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897014 | GTAAGCATGCAGATA[A/C]AAATGGAGAAGAATG | 11060 |
rs148043506 | snp | A/G | 6.59826e-05 | 0.00574343 | missense | WWP2 | GRCh38.p7 | 16:69939383 | TTGACAAAGTTGGCA[A/G]GGAAACCTGGCTGCC | 11060 |
rs148058314 | snp | C/T | 1.83461e-05 | 0.00302865 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842076 | AGTAGCTCCAGAGAA[C/T]CGGCACCAGCCCCCC | 11060 |
rs148061240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69816729 | CATGTACATACACAC[A/G]TGCACACGTATACAT | 11060 |
rs148077590 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69853985 | TCTGAAAGTGCACCC[A/G]TAGGAGGAGGAATGA | 11060 |
rs148129672 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WWP2 | GRCh38.p7 | 16:69857811 | AGACTACAGGTGTGC[A/G]CCACCATGCCTGGCT | 11060 |
rs148131948 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69791934 | GAATTTTCTTACCAG[C/G]GTGGAAAGAGCCAGC | 11060 |
rs148184545 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69795322 | TAGATGGCATTTATC[C/T]ATAACCTTTGGTGTC | 11060 |
rs148199897 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69893646 | TCCCAGGTTCAAACA[A/G]TTCTCCTGCCTCAGC | 11060 |
rs148201987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69833171 | GCCTTTTTAAGCCAT[C/T]GGTTTGTCTGAGTCA | 11060 |
rs148216757 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69935211 | GAGTGTCCCACCCGG[A/C]TCCCCTCTTAGGAGG | 11060 |
rs148222691 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69780535 | AAATTACGCGTCTTT[A/G]ACTCTGCCGGAGGTT | 11060 |
rs148274265 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69783972 | AAAAACATAAGATAC[A/G]AAGGCACAAGAATTT | 11060 |
rs148289173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882088 | GCCTCCGAAAGTACT[A/G]GGATTACAGGCATGA | 11060 |
rs148290400 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69820586 | AGGACCACACGTATT[A/G]TATATTGTGGCCTTG | 11060 |
rs148321380 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69877152 | ATAGAAGGCTCTTTC[A/G]TCAACATTGAAAAGC | 11060 |
rs148336938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909104 | TTGATGCATTCCGCC[A/G]TACCCTATGCCCAGC | 11060 |
rs148356857 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69921515 | TCTGCCTCAACACAC[A/C]CCTTCTCCAGTTCCT | 11060 |
rs148357489 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69861464 | TTCCGGAAGTCTTTC[C/T]GTAATTTAGAATGGA | 11060 |
rs148390994 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69855240 | GTTTCATGAAGTTTT[C/T]CTTCACCCTTAACTT | 11060 |
rs148410532 | in-del | -/TTTATTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866271 | AAAAAGGTTTCACAT[-/TTTATTTA]TTTATTTATTTATTT | 11060 |
rs148442810 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69860189 | CAGGCGTGGTGGTCC[A/G]ATTCCATTCTTTAAA | 11060 |
rs148445140 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69793507 | GTTTTTATAGACAAT[G/T]TGACAGGTAGGGGAC | 11060 |
rs148459897 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69890058 | TTCCTGGGCTCAAGC[A/G]ATTCTTCCACCTCAG | 11060 |
rs148496890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69797246 | ATGAAGGCTATGAGC[A/G]GAAGAAGAAATGTAG | 11060 |
rs148510071 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69895085 | CTACCCCCCTGCCCA[A/C]TTATGGATATCCAGA | 11060 |
rs148513444 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834130 | TCAAAACCCTGTAAC[A/G]GAGTCCCGTCCCATG | 11060 |
rs148521751 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | WWP2 | GRCh38.p7 | 16:69888946 | CCTGACCTCACATCA[C/T]CCACCTGCCTCGGCC | 11060 |
rs148531185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846670 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 11060 |
rs148550187 | in-del | -/ATTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866278 | TTCACATTTTATTTA[-/ATTT]TTTATTTATTTATTT | 11060 |
rs148578683 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941797 | AGTCAAGAGGACTCC[A/G]GGCCTCACAGACCCT | 11060 |
rs148580731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873102 | GAGATAGTTTTCTAG[G/T]GCTCGTGACAGCAGA | 11060 |
rs148585012 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69784960 | AGAAAGAGTGGTCGA[A/G]TGCAGTGGTTCACAC | 11060 |
rs148597935 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69882880 | ACAGCAGACCGGGTG[C/T]GGTGGCTCATGCCTG | 11060 |
rs148604553 | in-del | -/AC/ACAC | 0.300169 | 0.244914 | intron-variant | WWP2 | GRCh38.p7 | 16:69795259 | AAAAAAAATGCGGAT[-/AC/ACAC]ACACACACACACACA | 11060 |
rs148636331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69789565 | CTGCAGTCCTTCAGT[A/G]CTCCTCCTTGGAAAA | 11060 |
rs148649048 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69910982 | ACTTTGAGCCTCTAG[C/G]TCTCATTTCTGCTCT | 11060 |
rs148652320 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69826364 | CAAGGCCAGGAGTAC[C/G]AGACCAGCTTGGCCA | 11060 |
rs148667466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926231 | AAAGGGTCATTAGAG[A/T]TGATGAGACTTAGCG | 11060 |
rs148673417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69775172 | AATTTAACAAGTCCT[A/G]TTTGTTCAGATTCTT | 11060 |
rs148704213 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69831289 | TCCTTTGACATGCAC[A/G]TACATTTCGGTGGTA | 11060 |
rs148704349 | in-del | -/GGC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826963 | AAAAAAAGGGGGGGG[-/GGC]GGAGAGAATAATGGA | 11060 |
rs148707134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766365 | TGGCTGGCCTTCACT[G/T]TCTCCACACAGGACC | 11060 |
rs148720576 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69867289 | CTCACCAGCAGGTGG[C/G]TTCCCCAAAGCAGCA | 11060 |
rs148773177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69870453 | CTACAGGCATGCACC[A/G]GTAGTGCAGCTAGTT | 11060 |
rs148777460 | in-del | -/TGAACAAGTCAATATT | 0.0581099 | 0.160244 | intron-variant | WWP2 | GRCh38.p7 | 16:69899951 | TATATTGTAAATACC[-/TGAACAAGTCAATATT]TATCTACAATGTTAT | 11060 |
rs148789526 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903490 | TAAAAGAAAAATGGC[A/C]GGGCGCAGTGGCTCA | 11060 |
rs148812947 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799695 | GTGTGTATACGTATA[-/TG]TGTGTGTGTGCATGC | 11060 |
rs148825054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896945 | CATCTACCAAAAGTT[C/G]ATAATCTTCCAGTAT | 11060 |
rs148828730 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69811647 | TAGTCCCAGCCACTT[A/G]GGAGGCTGAGGTGGG | 11060 |
rs148841517 | snp | A/G | 0.000100358 | 0.007083 | intron-variant | WWP2 | GRCh38.p7 | 16:69939458 | GGGGGCCTCAGACCC[A/G]ATGAGCTCCTGGGAC | 11060 |
rs148843745 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69907112 | AAGCAGGTGTCAGAA[C/G]TTGGAGCTTGTGAGT | 11060 |
rs148844768 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69848252 | GGTCGGAAGTTCAAG[A/T]CCAGCCTGACCAACA | 11060 |
rs148896438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69852364 | TTACTGCACCCTCCA[C/T]CTCCTAGGTTCAAGT | 11060 |
rs148899502 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69786204 | GGCTGGAGTGCAGTG[A/G]CACGATCTCGGCTCA | 11060 |
rs148914194 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69884047 | TTCCTATTCTGCTCA[C/T]CTTCAGTTTCCTCCT | 11060 |
rs148940139 | snp | C/T | 0.000231604 | 0.0107586 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937583 | GGAGATAGACATGAG[C/T]GACTGGCAGAAGAGC | 11060 |
rs148979968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927418 | TCCACATCTGCCCTC[A/G]GCAGCCCTGACCCTG | 11060 |
rs148985827 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838425 | CTTGGCGTAATAGAG[A/G]AGGGAGACCCTCCTT | 11060 |
rs149032809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934325 | CCCCGTGGACTGGCT[C/T]ACCCTCTCGGGGCTC | 11060 |
rs149034347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868910 | GTTGTTGTTGAGACA[C/G]AGTCTCTCTCTGTGT | 11060 |
rs149039014 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69779850 | TATAATCTTTCCTGC[A/T]TTATTCAAGATACGA | 11060 |
rs149053176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69877953 | GCTGGGATTATAGGC[A/G]CGTGCCACCGTGCCC | 11060 |
rs149055420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815903 | GCTAAGACTACAGGC[A/G]TGTGCCACCATACCA | 11060 |
rs149103338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69905156 | ACACTGCTTGGCAGC[A/G]CTCTCTGAGCCTCTC | 11060 |
rs149107426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69820107 | GTGTGGTTGTCCACA[C/T]CTGTAGTCCCAGCTA | 11060 |
rs149120416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69915058 | AGCGGGTGTGAGATG[A/G]ACACACAACTGTCCC | 11060 |
rs149124319 | snp | A/G | 0.030278 | 0.119257 | intron-variant | WWP2 | GRCh38.p7 | 16:69857197 | CAACCTCTGCCTCTG[A/G]GGTTCAAGCGATTCT | 11060 |
rs149174633 | in-del | -/C | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69878895 | GTGTGTATTAGCAGA[-/C]CGTCTTTCTAAGAGG | 11060 |
rs149176571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861342 | ATTGGACAAGTCACC[A/C]TTTACTATACCTTCT | 11060 |
rs149178560 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69794836 | GAAGGGAGGATGTTC[C/T]AGATTTTAAAAGATT | 11060 |
rs149179355 | snp | C/T | 0.000115579 | 0.00760107 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799270 | TGTCAACCTCTCCAA[C/T]GTCTTGAAGAACAAT | 11060 |
rs149180372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69772148 | GTATTTTTAGTAAAG[A/G]CAGGGTTTCATCATG | 11060 |
rs149191771 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69891377 | GTGGCAAAGGGATTG[A/G]AGTGCTATCTCTTAG | 11060 |
rs149197310 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69807196 | ACACGTCACCATGCC[C/T]GGCTAATTTTGTATT | 11060 |
rs149279308 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69889192 | AAATGTGGGCACAGT[C/G]ACCTGTGCCTGTAGT | 11060 |
rs149281174 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69830630 | GCCAGAGTGTGAGTG[C/T]TGGGGGGCCGCGGGG | 11060 |
rs149281767 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893552 | TAGTTCAGAATGCTG[-/T]TTTTTTTTGTTTGTT | 11060 |
rs149295939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931087 | CTTTCCTTAGGGCTG[A/G]CAAAGACAAATTGTT | 11060 |
rs149299936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841795 | CAATGTCTTGGAGAA[A/G]AGAAGCTGTTTCCAA | 11060 |
rs149346273 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69936936 | CAAAGACTCCGGTGT[C/G]TGCAGGTCACTGTGA | 11060 |
rs149351825 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69846025 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGCCAGA | 11060 |
rs149353616 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69781729 | TAAAGAGACTAGGTA[A/G]TTTATAAAGAAAAGA | 11060 |
rs149368729 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879377 | TAAACAATAACATTT[C/G]CCCCCAACCTGACCG | 11060 |
rs149406237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784528 | GTTGCTGTGGTCATG[A/G]TATCCTTCACCACAC | 11060 |
rs149422868 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822205 | CTTAAGAGTTTCTTC[C/G]TGTTGGGTCAGGGTT | 11060 |
rs149438486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918389 | AGATCAGGGATTGGC[A/C]AATAATAGTCCATGG | 11060 |
rs149488844 | snp | A/T | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924522 | CCCCTTCCCCGCAGG[A/T]TATGAGAATGCCTGG | 11060 |
rs149500742 | snp | C/G | 5.02037e-05 | 0.00500993 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871840 | TTCAGCCAGAACAAC[C/G]CCAGCAACCGGCGAG | 11060 |
rs149510406 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69871248 | ATGATCGTGCCACTC[C/T]AGCCTGGGCAGCAGA | 11060 |
rs149512637 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69808307 | TGGGATCTCGCTATA[G/T]TGCCCAGGCTGGTCT | 11060 |
rs149559338 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897929 | ACAAAACAAAACAAA[A/T]CAAAACAAAAAAAAC | 11060 |
rs149565006 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69812866 | CACTGCAAAATTACT[A/G]TTTCCCCTTGTCAAT | 11060 |
rs149577924 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69908664 | TCTTTGATGCTTCCT[G/T]TAAATTAGCCACATG | 11060 |
rs149580594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849981 | GCCAGATGTGGCATG[C/T]GCCAGAAAGCTGGTT | 11060 |
rs149630325 | in-del | -/CT | 0.093777 | 0.195178 | intron-variant | WWP2 | GRCh38.p7 | 16:69792449 | CATAAAGTCGTGACT[-/CT]GTGTATAAAGATATA | 11060 |
rs149631835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854972 | GTGATCCTCTTGCCT[C/G]AGCCTCCCAAATAGC | 11060 |
rs149634116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788476 | CTACATTCTCTGTGC[A/C]CCAGCCTCCTTGCTC | 11060 |
rs149647457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69885779 | TGGGGATATCAATTG[C/T]AACTAACTTGTGGGG | 11060 |
rs149653021 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69798251 | AGATGTATATGTTCA[C/T]GGTAATTTCCCCAGA | 11060 |
rs149664432 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69847947 | GCCCACAGGACTGTC[G/T]GTGAGTGGAGCTGCT | 11060 |
rs149667071 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782442 | TGAGGCAGGACTGGT[A/G]TCCCCAGAGCTGAGG | 11060 |
rs149685425 | snp | A/G/T | 0.0217236 | 0.101931 | intron-variant | WWP2 | GRCh38.p7 | 16:69793331 | CACTCCAGCCTGGGT[A/G/T]ACAGAGCAAGACTCC | 11060 |
rs149732292 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | WWP2 | GRCh38.p7 | 16:69883990 | TATATGTTACTAAAA[C/G]TTTAAAAAAATAAAA | 11060 |
rs149754368 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69833989 | CACTGCCATCACCTT[C/T]GCCCAAACCACCATC | 11060 |
rs149756530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770784 | GCTGGTGTCTGCCAG[C/G]TGCAGAATTGATTGC | 11060 |
rs149770549 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69869587 | TTGAGCTCAAGTGCC[A/G]TCCCATCTCAGCCTC | 11060 |
rs149802925 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | WWP2 | GRCh38.p7 | 16:69927153 | AATTAAGAGGAAGAA[A/C]ATTCTGGCTAAAGGC | 11060 |
rs149805419 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937181 | AGCCTTCCTGGATGG[C/G]TTCAACGAGGTGGCC | 11060 |
rs149808755 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69776551 | ATAATGATAATAGGC[C/T]GGGCGCAGTGGCTTA | 11060 |
rs149839001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906590 | CGTGATGCAAAATTA[C/T]GCAGTTAAAAACCAT | 11060 |
rs149858454 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | WWP2 | GRCh38.p7 | 16:69771318 | CAGTGTGCTATCTTG[A/G]CTCACTGCAACCTCC | 11060 |
rs149893009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910652 | TTGACCTTGTGATTC[A/G]CCTGCCTTTGCCTCC | 11060 |
rs149894832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69850847 | TGGGTGAAATCTGCC[A/G]TGTTTTTTTTAGAGC | 11060 |
rs149898927 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760532 | AGTTTTAGTAGAGAT[A/G]GGGTTTCACCAGGTT | 11060 |
rs149946511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856388 | GTGATGGTAACACCA[C/T]TATAAACATTTGGTA | 11060 |
rs149948241 | in-del | -/TAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826721 | TCTCTCTAATAAAAA[-/TAC]AAAAAAAAAAAAAAA | 11060 |
rs149948842 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69790073 | TGTGGTAAAACCCTG[C/T]CTCTACTAAAAATAC | 11060 |
rs149950952 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69766123 | AAATTGAGCCCTACA[C/G]CTGCCCCTCAGACAG | 11060 |
rs149965395 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69866987 | GGACTACAGACATGC[A/G]CCACCAGGCCTGGCT | 11060 |
rs149980375 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | WWP2 | GRCh38.p7 | 16:69815128 | CTGCCTCAGACTCCT[A/G]AGTAGCTGAGATTAC | 11060 |
rs150033402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69903046 | TCAAAAAAGGTGATG[A/G]AAGAAAGGTCTTGTT | 11060 |
rs150034486 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69843253 | GGTTAAGACCTCCTA[C/T]GCTTAGAGTCCAAAT | 11060 |
rs150059700 | snp | C/T | 0.000576811 | 0.0169727 | missense | WWP2 | GRCh38.p7 | 16:69798759 | GCGGTGGATGGACTC[C/T]CCAGTGAGACCAAGA | 11060 |
rs150082808 | snp | A/G | 0.00251191 | 0.0353503 | missense | WWP2 | GRCh38.p7 | 16:69939120 | GGATTTGCCGAACTC[A/G]TCGGTATGTTTTCTC | 11060 |
rs150110970 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850703 | TGTATTTGAGGAAAT[-/A]AAAGTCATTTAGAAA | 11060 |
rs150119897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841704 | GGTTAGGGTTTTGTT[C/G]TCTATCTCACGTTTT | 11060 |
rs150121644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777205 | ACAATATACATATGG[A/C]GATATCATATATGCA | 11060 |
rs150187963 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69879216 | AAATTGTAGTGAAAA[A/T]CACATAACATGAAAT | 11060 |
rs150190478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817200 | TCACCCAGTTTTTTC[C/T]GCATCAGTGAAACTA | 11060 |
rs150210700 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762135 | GAGTAGGTGGCATTC[A/G]GTGAGCCCTCAATTT | 11060 |
rs150255976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69918105 | TGTTTAAGGAATCAA[C/T]GTGTCTAAAACTGAA | 11060 |
rs150257765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69857928 | GTTGGGATTATAGGC[A/G]TAAGCTACCGCATCC | 11060 |
rs150261831 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69769045 | GAGTGCAGGCTGGGC[A/G]CAGTGGCTCACGCCT | 11060 |
rs150275349 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69868456 | ACCCGGGGCTGGAGT[G/T]GATCATGGACATGTC | 11060 |
rs150278261 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69802081 | ACTACAGGCACCCAC[C/G]ACCATGCCCGGCTAA | 11060 |
rs150344950 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | WWP2 | GRCh38.p7 | 16:69905093 | TGTAGCTGTTTAGAT[G/T]ATTTCTCTACCTTGC | 11060 |
rs150346264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845622 | CTGCTTGGTAAAGCT[A/G]TAGAACTGGAACTGT | 11060 |
rs150363676 | snp | C/T | 9.2879e-05 | 0.00681402 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842091 | CCGGCACCAGCCCCC[C/T]AGCACAAACTGCTTT | 11060 |
rs150400933 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | WWP2 | GRCh38.p7 | 16:69784169 | CAGTGGCATGATCTC[A/G]GCGCACTGCAACCTC | 11060 |
rs150466869 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | WWP2 | GRCh38.p7 | 16:69884605 | TGCACTCCAGCCTGG[G/T]TGACAGAGCAAGACC | 11060 |
rs150472150 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69797916 | AAAATTATAAATTTT[C/G]TTATGTTCCCAGGCT | 11060 |
rs150489581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835607 | AATTTGTTTTATCTA[C/T]ATGTTATTATAGTAT | 11060 |
rs150501870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69880284 | GTGATTTTTTTTTTA[A/G]TGTTGATCACTTTTA | 11060 |
rs150522266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830391 | ACTGTGCCCAGCCCA[G/T]GAAATGTTTCCTGAA | 11060 |
rs150525136 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69765112 | GAGGTGGGAGGATCA[C/T]CCAAGCCTGGGGAGG | 11060 |
rs150528209 | snp | A/C | 6.60393e-05 | 0.00574589 | missense | WWP2 | GRCh38.p7 | 16:69787060 | CCCTGCCTTTTGAGA[A/C]GTCTCAGCTCACTTT | 11060 |
rs150537512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930811 | CAGGAATTCGAGGCC[A/G]CAGTGAGCCATGATC | 11060 |
rs150569142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919850 | CAGGGTGGAGTGCAG[C/T]GGCATGATCATGGCT | 11060 |
rs150577064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770502 | ACATGCCTCGCCCTA[C/T]GTCTCTTCATTTGTA | 11060 |
rs150590735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69869331 | CTCCAGAGTTTGCTA[C/T]GTTTCTCCCTTTTTC | 11060 |
rs150593804 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69806271 | AATTTCTAGAATATA[A/C]CTAGTTGCTCAAGAT | 11060 |
rs150595587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781419 | GGCACAATCTTGGCT[C/T]ACTGCAGCCTTGACC | 11060 |
rs150645041 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | WWP2 | GRCh38.p7 | 16:69810553 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 11060 |
rs150660759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69847164 | ATCTCGGCTCACTAT[A/G]AACTCTGCCTCCCAG | 11060 |
rs150663613 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69821809 | GCAATCCTCCCATCT[C/T]GGCCTCCCAAAGAGC | 11060 |
rs150711615 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69850467 | CAGATGCATGGATGA[A/G]TTAGAGTCTAGTGTG | 11060 |
rs150728083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69883137 | CAGTTTGGGTGGCAG[A/G]GTGAGACTCCATCTC | 11060 |
rs150730784 | snp | C/T | 0.030278 | 0.119257 | intron-variant | WWP2 | GRCh38.p7 | 16:69862214 | GGGATTACAGGCATT[C/T]GCCACCATGCCCGGC | 11060 |
rs150732957 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | WWP2 | GRCh38.p7 | 16:69795579 | CAAAATGATAACAAT[C/T]GGTGAAGAGTATACA | 11060 |
rs150747884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69893921 | CACGGCTCCTCTTCA[C/T]TGAGGCATTTGAGCT | 11060 |
rs150785002 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69799082 | GTTTTGGTTCCCCCT[C/T]CCCAAGATGTCAGCA | 11060 |
rs150798286 | snp | C/G | 0.077417 | 0.180873 | intron-variant | WWP2 | GRCh38.p7 | 16:69897798 | CTGTAGTCCCAGCTA[C/G]TCAGGAGGCTGAGGC | 11060 |
rs150801833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836642 | TTGAGACAGGGTCTC[G/T]CTCTGTCACACAGGC | 11060 |
rs150814804 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940445 | AAGGTCTGAGGGAGC[A/G]GGCCCTGGGGCGAGG | 11060 |
rs150854200 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69842726 | CTACGCTGGAGTGCT[A/G]TGGCACCATCACAGC | 11060 |
rs150871122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877284 | CTGTGTTTGAGGGAT[C/G]TTTCCTTAAACCTCA | 11060 |
rs150875402 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69788151 | GAGGATCACCTGAGC[C/T]CAGGAGTTTGAGACC | 11060 |
rs150891468 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | WWP2 | GRCh38.p7 | 16:69825228 | CTAGGAGTTCGAGAC[C/T]AGCCTGACCAACATG | 11060 |
rs150956103 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69874687 | TGGGATGATTTACTT[C/G]CTAATTCTTTATTGA | 11060 |
rs150958403 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | WWP2 | GRCh38.p7 | 16:69812206 | GAGTCTCGTTCTGGC[A/G]CCCAGGCTGGAGTGC | 11060 |
rs150973729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907256 | CTGTGGGTTTTGTGC[A/C]TTCTTGTGTAACTAG | 11060 |
rs151023715 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69911927 | ATCCACCAGGAAGCC[A/G]GCTGATGTGCACCAT | 11060 |
rs151046442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69864239 | TGGACATGGTGGTGC[A/G]CACCTGTGATCCCAG | 11060 |
rs151047801 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69797373 | GATGTGGAATCAGAC[C/T]GGCCGGGTGCACAGT | 11060 |
rs151061728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895738 | GCCCTTCAGCCTGGA[A/T]GACTGAGTGAGACCC | 11060 |
rs151115785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69898892 | TGTATTTAGTAGAGA[C/T]GGGAATTCACCATGT | 11060 |
rs151117948 | snp | C/T | 0.000545293 | 0.016503 | intron-variant | WWP2 | GRCh38.p7 | 16:69840315 | CAGGGTGGGGCTGGG[C/T]GGGGGCCAGGAGGTG | 11060 |
rs151164797 | in-del | -/AGC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914431 | CCATCCTTCTTCTCA[-/AGC]GCTGTAGAGCAGGAC | 11060 |
rs151169961 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69844860 | AACTATTCATTCTGC[A/G]CTCACATGGAACCTG | 11060 |
rs151186597 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | WWP2 | GRCh38.p7 | 16:69878064 | CCACCCGCCTCAGCC[C/T]CCCAAAGTGTTGGGA | 11060 |
rs151190030 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | WWP2 | GRCh38.p7 | 16:69789716 | CCTGTTTCCCTACAT[C/T]TTTACCAGCACAATG | 11060 |
rs151253165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915442 | AATGAGCCAGGCTTG[A/G]TGGTGCACACCTGAG | 11060 |
rs151257965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69831618 | CGTACAAACTCTTCT[C/T]AATAGGAAATTATTA | 11060 |
rs151271484 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932654 | AAGTCAGGTGTCCCC[A/G]TGTGGATAAGCTGTG | 11060 |
rs151276774 | in-del | -/TTG | 0.0130921 | 0.0798413 | intron-variant | WWP2 | GRCh38.p7 | 16:69938043 | TTATACGTATGGGTT[-/TTG]TTGTTGTCGTTATGA | 11060 |
rs151309319 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69835374 | TAGTCCCATTATGTA[G/T]TATAGGGTTCCTCTG | 11060 |
rs151311879 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69772664 | TTCTAGAAAAGTGGT[A/T]ACTTCTGGGGCATTA | 11060 |
rs151324200 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938699 | TCTGGAACATTTCAT[A/C]TCCCCAAAAACCTTA | 11060 |
rs151325725 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | WWP2 | GRCh38.p7 | 16:69870539 | CTCCTGGGCTCAAGT[A/G]ATCCTCCCGCCTTGG | 11060 |
rs151329313 | in-del | -/AGG | 0.0581099 | 0.160244 | intron-variant | WWP2 | GRCh38.p7 | 16:69900419 | AGATTGCTTGAGCCC[-/AGG]AGTTCAAAACCACCC | 11060 |
rs180693146 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69934292 | TTCACCAGGAGGCAG[C/T]GTGGCGTGAACGGCA | 11060 |
rs180763979 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69797474 | TAAAATGGGGTGATG[A/G]TATATTCCCTGCCTC | 11060 |
rs180791167 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69805430 | TAGTTGCTTTGCATA[A/G]AACTTTCTGTTTTAG | 11060 |
rs180793796 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774289 | TGAGACAGGGTCTTG[C/T]TCTGTCACCTAGCTG | 11060 |
rs180797868 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761089 | TGCACTCCTGCCTGG[A/G]CTACAAGAGTGAAAC | 11060 |
rs180814552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841955 | AGTTCTGTTCCTGGC[C/T]GTCAAATCTCAAACA | 11060 |
rs180814866 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69783873 | GGTGAGAGGATTGCT[C/G]GAGTCTAGGAGTTCA | 11060 |
rs180815113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69901065 | GTTTACAAAGGACCT[A/G]CTGAAGCACTAAACA | 11060 |
rs180818736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908954 | GTAGCATAGCACAGT[A/G]ACGTTTATTCCGGGT | 11060 |
rs180822004 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69816012 | AATTACTCACCATTC[G/T]TCAGCTGAGGAGGCA | 11060 |
rs180825051 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830251 | ACAACCACCATGCCC[A/G]GCCTAGTTTTTTTCT | 11060 |
rs180828213 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69891336 | AATCTGTCATTTCTA[A/T]TTCCAATACCAACAA | 11060 |
rs180831374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851244 | GCTGGTCTTGAACTC[C/T]TGGACTCAAGTGATC | 11060 |
rs180833560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875690 | ATCCATAAGACACAA[C/T]TCCTAATCTATTCCA | 11060 |
rs180838119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862048 | TATAGGAGGAAAATC[A/G]ATAATCAGGTTGTTT | 11060 |
rs180856089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882483 | TACGGACAATGTAAA[C/G]CATATAAGATAAGGC | 11060 |
rs180894195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917290 | ACTTCCTATTGTCTT[C/T]GGGTCCAAAATAATA | 11060 |
rs180971731 | snp | C/T | 5.78397e-05 | 0.00537741 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939942 | TTGGACAGGAGTAAC[C/T]GAGGCCGCCCCTCCC | 11060 |
rs180977550 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69912279 | CCTGGACGACAGAGC[A/G]AGACTCCATCTCAAA | 11060 |
rs180985978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879193 | TATATTCTAGGTACA[A/G]TTTTTAAAAATTGTA | 11060 |
rs180990304 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69904515 | GTACGATTACAGGTA[C/T]GTGCCAGCACATCTG | 11060 |
rs181001248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69894745 | CTCAGCGCTCAGCCC[A/G]CTTTGGGGACCCAGT | 11060 |
rs181021409 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857167 | GGAGTGCAGTGGCGC[A/C]ATCTCGGCTCATTGC | 11060 |
rs181092600 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773885 | TTTAGTGCAGTCACA[G/T]TAGTTGAGGTTTCAA | 11060 |
rs181097435 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796483 | TGCCCCTGTGATCAC[A/G]TGGCTGACTGGTGTT | 11060 |
rs181097606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815393 | GCTCACTGTAACCTT[C/G]AACTCCTGGCCCTAG | 11060 |
rs181147206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829445 | CCACTCAGTCCTCCC[A/G]CCCATTTGGATCTCA | 11060 |
rs181151028 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850910 | TTCCCCACTATCAAC[A/G]TCCCCCACCAGAGTG | 11060 |
rs181166799 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69875214 | TACACTATACTATGG[A/G/T]CCATAAAAGGTACAA | 11060 |
rs181223424 | snp | C/G/T | 0.00239401 | 0.0345304 | intron-variant | WWP2 | GRCh38.p7 | 16:69819417 | GCTTTCCAGATCCCT[C/G/T]GGGCCACAGGTCTCC | 11060 |
rs181225005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69911738 | CATGTGTTTATTTCT[A/G]TTCTTCCTGAAAACC | 11060 |
rs181228689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69790366 | CATAAGGAGGAAAAA[A/G]ATTTTACTATTTATT | 11060 |
rs181230326 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69769232 | TGAGGCAAGAGAATT[A/G]CTTGAACCCGGGAGG | 11060 |
rs181232152 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69893846 | ACTGCACCCAGCCCT[C/T]AGAATGCTCTTCTCT | 11060 |
rs181234975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833994 | CCATCACCTTTGCCC[A/G]AACCACCATCTGCTC | 11060 |
rs181238083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69878939 | CCAAAGTAGTATAAA[A/G]TATTCATAAAGTGGT | 11060 |
rs181239257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856216 | GACATAGAAGCTTAT[A/G]TTCTATATGATTCCA | 11060 |
rs181239283 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69812794 | CTCATGACTCAGCTT[C/G]TTTATTATTGATGAC | 11060 |
rs181249665 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69938884 | CTGGGGTTTCTCAGG[C/T]TGGAGGCTGTCATCC | 11060 |
rs181289203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846743 | AAAAAAAAGAAAAAA[G/T]AATGGGAATAATGAA | 11060 |
rs181326491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926790 | TTGGCAGCAACTCCA[A/G]TGCGAGAGAGTAAAA | 11060 |
rs181338708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69887626 | GGCCAGGTGGATCTC[A/G]AACTCCTGACCTCAA | 11060 |
rs181374636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826547 | ATTGCACTCCAGGCT[A/G]GGCAACAGAGTGAGA | 11060 |
rs181397122 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69869941 | ATGGGGAACTTTCTA[A/T]TATAGCTCTTAATTT | 11060 |
rs181429139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69777458 | GGCACCTGCCACCAC[A/G]ACCAGATAATTTTTG | 11060 |
rs181447968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905788 | TTATAAATTTCAGTT[A/C]ATCTTCCTTTTCTGC | 11060 |
rs181476245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69776568 | GGCGCAGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 11060 |
rs181478010 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940424 | TCTGATGATGGAGAT[A/G]AAGTGAAGGTCTGAG | 11060 |
rs181559774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69869297 | TCTCCATTGCCATGC[A/G]GTGTTTAGGTATGAG | 11060 |
rs181588281 | snp | C/T | 8.25089e-05 | 0.00642243 | intron-variant | WWP2 | GRCh38.p7 | 16:69925521 | TGGCCCTTGGCCTTC[C/T]GTCAGCCACGGTGCT | 11060 |
rs181594430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69905143 | AGACTTGCCGCTCAC[A/G]CTGCTTGGCAGCGCT | 11060 |
rs181598647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886849 | CCTGTAAGAAACGTT[C/T]ACGAAGAATCTGGAT | 11060 |
rs181612835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913181 | AGGCACATGCCACCA[C/T]GCCCAGCTAATTCTT | 11060 |
rs181646418 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69788984 | TCTTGGGAATATTTT[G/T]CTTGAGTATTTTTGA | 11060 |
rs181658289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825879 | TTTTCTCACCTTGGC[C/T]TCTCCAAGTGTTGGG | 11060 |
rs181681155 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883574 | CAAACTTTCTTTTTT[C/T]CAACTTTAAGTTCCG | 11060 |
rs181704397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918446 | GTTAATAAAGTTTCA[C/T]TGAAACATAAGAACA | 11060 |
rs181706583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896366 | GCTCAAGCGATCCTC[C/T]TATCTTGGCCTACCA | 11060 |
rs181709232 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69864713 | AGCCACTATGCCTGA[C/T]GAATTTTTGCATTTT | 11060 |
rs181710775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902036 | TTTTAGCTTAATCCT[A/C]TTCTTGGTGAAATGT | 11060 |
rs181751504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812247 | TCTTGGCTAACTGCA[A/T]CCTCTGCCTCCTGGT | 11060 |
rs181777416 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69768600 | GGGCAACAAGAGCGA[A/T]ACTCCTTCTCAAAAA | 11060 |
rs181782008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768142 | CACAACTGGCTAGGG[C/T]TCTGGAATTTCTGAA | 11060 |
rs181810692 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69845299 | GTGCATGCCTACCCC[C/G/T]CTTCCCTGCTAAGCC | 11060 |
rs181828370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886009 | GATCGGGAAAGGGGG[A/G]TTGCCTAGAAACACT | 11060 |
rs181829086 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69788282 | TGTGATTGTGCCACT[A/G]CACTCCAGCCCAGGC | 11060 |
rs181831188 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69811355 | CTCACACCTGTAATC[C/T]CAGCATTTTGGGAGG | 11060 |
rs181838629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824972 | GATGGGGTTTCACTT[C/T]GTTGGCCAGGCTGGT | 11060 |
rs181841913 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908232 | CCTGGGCAACAGAGT[A/G]AGACCCTGTTTCATT | 11060 |
rs181851059 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69845786 | TGGGCGTGGTGGCTC[A/C]TGCCTGTAATCCCAG | 11060 |
rs181855695 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842815 | GCTGAGACAGCAGGC[A/G/T]TGTGCCACCATGCCT | 11060 |
rs181924378 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69842396 | GGGTATATTGCATGA[A/T]GTTGAAGTTTGGGCT | 11060 |
rs181929172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862589 | AACTTCTCTTTTGCT[A/G]AACTTGAATACCAGT | 11060 |
rs181947141 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882790 | AGTCCTTTTGGGGAG[A/C/G]TATGGGTGTACATCA | 11060 |
rs181950421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69806060 | AAAAAAATTAGCCAG[A/G]TGTGATGGTGTACGC | 11060 |
rs181953195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69822744 | ACACAGGAGGCCAAC[A/G]GCAGGGAGGAGGCAG | 11060 |
rs181962121 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801524 | ACAGATGCGAGCCAC[G/T]GCGTCTGGCCAATTA | 11060 |
rs181970465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69835795 | CATGCTCATATAAAA[C/T]CAAAGTAAATTTTTT | 11060 |
rs182060052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69784785 | TTTTGGGTGAAGTAC[C/T]ATTTTTACTTAAACA | 11060 |
rs182061029 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762223 | ACGATAAAAAGGCCT[C/T]CTCGAGGCCAGAGGT | 11060 |
rs182081316 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932978 | TCTGTTCGGTGGTGG[C/T]GTTGCCTTCTGCGCT | 11060 |
rs182093671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891056 | TAAGATGGCTAGGAG[A/G]GCTCTGTGGGCTGAC | 11060 |
rs182098457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877567 | TTCTCCTTTGCATTC[G/T]CAACTTGGCTAACTG | 11060 |
rs182103641 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900764 | CTTGACCTCAGGTGA[C/T]CTGCCCGCCTTGGCC | 11060 |
rs182111599 | snp | A/G | 4.94539e-05 | 0.00497238 | missense | WWP2 | GRCh38.p7 | 16:69936409 | CTGAAGGAGGGCGGC[A/G]AGAGCATCCGGGTCA | 11060 |
rs182113383 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | WWP2 | GRCh38.p7 | 16:69832544 | TTTTATTTTTAAAAA[A/T]TTTTTAATGTTTTTT | 11060 |
rs182119225 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69852853 | CTCATTTATTTTCAT[A/G]TTGTCTGTGGCTACT | 11060 |
rs182129663 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909988 | ACATATTTGTTGACT[G/T]ATTGTTTTTGGCTGT | 11060 |
rs182133223 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893022 | TCTCTGCCTAAGCCA[C/G]GATAACTTAACTTTA | 11060 |
rs182189973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918126 | TAAAACTGAATTCCC[C/T]GTCTTTCTTCCGAGA | 11060 |
rs182191167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785736 | AGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 11060 |
rs182242919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69820011 | TTAAGAGGCTGAGGC[A/G]GGGGCAGGGGATGGA | 11060 |
rs182264927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817707 | ATGGAGTCTCGCTCC[A/G]TCACACAGGGGTGTG | 11060 |
rs182291784 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773112 | CTAGTGTCGCTACTA[C/G]TTTGTTTCCTTAGCA | 11060 |
rs182303008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69814725 | CAGGCCAGTCATGAG[C/T]GGTGGGCCTCCTCCC | 11060 |
rs182307441 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69827114 | TCACTTGTTGACACT[A/C]CTGCATACATGTCTA | 11060 |
rs182309146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906158 | GCTCACTGCAAGCTC[C/T]GCCTTCCGGGTTCAC | 11060 |
rs182311416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69780715 | TGAGTCAAAACATCA[C/T]CTTTTTGGCCTGGTG | 11060 |
rs182311713 | snp | A/C/G | 0.000675294 | 0.0183642 | missense | WWP2 | GRCh38.p7 | 16:69888060 | ATGAACCCACAACAG[A/C/G]CACTGATCCCGAAGA | 11060 |
rs182316884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847360 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 11060 |
rs182320762 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69870146 | TTATCTGTAAAGCGG[A/G]GATAATAATATTAAT | 11060 |
rs182359947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69902626 | TGCAGTGTTGAGACC[C/T]GTGGGTAGTTTGATT | 11060 |
rs182420983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828794 | TAAATATGGGAGTTT[C/T]CTATTATTCCATCCT | 11060 |
rs182460698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69901506 | CAAGCTCTGCCTCCC[A/G]GGTTCATGCCATTCT | 11060 |
rs182526526 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69823551 | CTTGTTCACTGCAGC[C/T]TGTGCTCCTGGGTTC | 11060 |
rs182543149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865288 | CTCCCGACCTCAGGT[A/G]ATCCGCCTGCCTCAG | 11060 |
rs182552386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775554 | GCCCATCTATTCTCA[C/T]GTGTTGTCTGCTGTT | 11060 |
rs182559199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795413 | ATTTAAAAATCATAT[C/T]CTTATTTGCACTAGC | 11060 |
rs182630707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884010 | AAAAAATAAAAGCTT[A/G]GACAGTATAAAGAAT | 11060 |
rs182674678 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838931 | AGATCTTTGACTTGA[C/T]CCAGAATTTTCTGCT | 11060 |
rs182716735 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69906307 | TTGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT | 11060 |
rs182721546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69888767 | TGGAGTGCAATGGCA[C/T]GATCTCAGCTCACTG | 11060 |
rs182723847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69880458 | CATACATTTTCAAAA[C/T]AAATTTCAGACTTTG | 11060 |
rs182727926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914460 | ACCTTCACAATTCCG[A/G]TGGAAAATGATTTCC | 11060 |
rs182741457 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69880589 | GCTTCGTCCATTTTT[A/T]AGTTTTGCTCCTTTT | 11060 |
rs182744248 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838128 | ACCAAGAGGAATTAG[A/G]ACTCTTCCTAAACAC | 11060 |
rs182744444 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941796 | CAGTCAAGAGGACTC[C/T]GGGCCTCACAGACCC | 11060 |
rs182750263 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69913671 | AAAATAATGGCATCT[G/T]TGCAACAAGAACAGG | 11060 |
rs182753073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859301 | CTCACGCCTGTAATT[C/T]CAGCACTTTGGCAGG | 11060 |
rs182760139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898692 | TTAATCTGCAGGATT[A/C]TTTTTTGTTGTTGTT | 11060 |
rs182800017 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69843266 | TACGCTTAGAGTCCA[A/G]ATATTATACTTGTTA | 11060 |
rs182834177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807302 | AGTCTCCCATACTGC[C/T]GGGATTACAGGCGTG | 11060 |
rs182842134 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808239 | TCTTTGAGATTAAAG[A/T]TATATGACCTTTTTT | 11060 |
rs182857354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762708 | GGCATGGAGAGGAGC[A/G]ATCTTTGTGGAGGGA | 11060 |
rs182901310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930727 | TACATTTAAAATTAG[C/T]TCGGTGTGGTAGCAC | 11060 |
rs182964376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860692 | TGAATTCCTGCCTTG[A/T]GATTTGTCGTGTCAG | 11060 |
rs182965101 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779516 | CCTTCTTTAGAATTT[A/G]TCTGATTGTTTTAGT | 11060 |
rs182996580 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821777 | GTGTCAGGCTGGTCT[C/T]AAACTCCTGGCCTCA | 11060 |
rs182997788 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69857693 | TTGAGACAGGGTTTC[A/G]CTCTGTCACCCAGGC | 11060 |
rs183005189 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780009 | ATATTTGCCCCAGAA[C/G]TTTTTTCTTTGAAAG | 11060 |
rs183016869 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69899854 | GATGGCATTTTAGAT[G/T]TGATGAAAAACAATA | 11060 |
rs183018781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928637 | AGGCAGGCCAGGCAC[A/G]GTGGCTTATTGCCTG | 11060 |
rs183019517 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69802166 | ATCTCCTGACCTCGT[A/G]ATCTGCCCGCCTCGG | 11060 |
rs183022932 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69820947 | CAGTGTCCGGCTCAC[C/T]TCGGAGGCTGACAGC | 11060 |
rs183033269 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | WWP2 | GRCh38.p7 | 16:69820323 | CTCAGCTCACTGCAA[A/C]CTCCGCCTCCTGGGT | 11060 |
rs183039171 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837725 | ATCAAGGAGCCTTCC[A/G]GAATGCTCATCCCTC | 11060 |
rs183083783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889461 | AATCAGACAGCTCTG[C/G]GTTTGAATCCCCCCA | 11060 |
rs183118588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791250 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTAT | 11060 |
rs183123444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69852522 | CAGGTGATCCGCCCA[C/T]CTCGGCCTCCCAAAG | 11060 |
rs183124435 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69785072 | GAAACCCCATCTCTA[A/C]TAAAAATACAAAAAT | 11060 |
rs183128432 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69813016 | TATTTTTGAATTCCA[C/T]CCTTCCTTCTGCATT | 11060 |
rs183144903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798104 | CACTCTGTGATGTCT[A/G]GTAAAATGAATATTC | 11060 |
rs183151343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817272 | GTTTTGTTTTTTGAG[A/G]CAGTCTCATGCTGTC | 11060 |
rs183160847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832060 | TCTCGAACTCCTGAG[C/T]TCAAGCGAACCATCT | 11060 |
rs183193523 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69906855 | ACCACACTCCAGCTC[A/G]GGCAACAGAGCAAGA | 11060 |
rs183244485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69764139 | AAATGAGTAGGGACT[C/T]AAGCCCAGACCCTTA | 11060 |
rs183249484 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69786361 | ATCTTGGCCAGACTG[G/T]TGTTGAACTCCCAAC | 11060 |
rs183262783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808915 | GCTTTGGTTCATAGG[G/T]TGGATGTATGCTTAC | 11060 |
rs183282120 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803121 | TTTTTCCTATTTGAT[A/G]ACTATTAACATTATG | 11060 |
rs183354097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903084 | CAACTATTCTTCTCG[C/T]TAAGCCAGTTGAGGG | 11060 |
rs183355690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823873 | TCTAGAAACTTCTTC[C/T]ATTCCTCTTGAGCCT | 11060 |
rs183357199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69872507 | GACGTGAGCCACTGC[A/G]CCTAGCCTTTCTATT | 11060 |
rs183361120 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69843416 | AAGAGATGAGGGGAG[A/T]GGGTTGGCACCTTTG | 11060 |
rs183363254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935046 | GTGAATATGGAAAGG[A/G]AGGTCCTGCCACGTG | 11060 |
rs183365171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884671 | GAAATATTTTAAAAC[A/G]TATTTGAATCCAGTG | 11060 |
rs183367286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909111 | ATTCCGCCGTACCCT[A/T]TGCCCAGCCTGTCCC | 11060 |
rs183369045 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69865514 | CTTCATTTCTAAAGG[C/G]GGGGTACCATAACCT | 11060 |
rs183399405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69827701 | CGGTTGTGGCCGCTG[C/T]GGTTCCCTGAGGGCA | 11060 |
rs183428414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69791965 | TTGATAATACTGGTG[C/T]ATCTCATTATACACA | 11060 |
rs183526881 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69939255 | CTGCATCCTGGGGCC[A/G]AGCCCATCTGTGGGT | 11060 |
rs183532758 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69911753 | ATTCTTCCTGAAAAC[C/T]CACTAAAATAGTAAT | 11060 |
rs183576515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877182 | CTGTTGTTTCGTGTG[A/G]CCAACCCCGTCAATG | 11060 |
rs183612284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909431 | GGAGGGAAAGGCTGT[A/C]GGAAGTAGGGACTCT | 11060 |
rs183613500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813646 | TTTATTTTTTGTATT[C/T]TTGTAGAGACAGGGT | 11060 |
rs183633946 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809806 | AGAGAGAGAGAGAGA[C/G]AGATAGGAAGGAAGG | 11060 |
rs183640264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847964 | TGAGTGGAGCTGCTC[C/T]TCCTAGCACCTCACG | 11060 |
rs183646428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824748 | TGGGCCTAGAATGAC[C/G]TCAACTTTGCACCTG | 11060 |
rs183654391 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | WWP2 | GRCh38.p7 | 16:69770996 | AAAAAAGGTAGTATT[C/T]TGTGTTGTGAGAGTA | 11060 |
rs183656552 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69879394 | CCCCAACCTGACCGG[C/T]CCCCGCCCACAGCCC | 11060 |
rs183691416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770390 | CCATAAAAACCCTGA[A/G]GGACTGGGTTTGGGG | 11060 |
rs183755255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69788147 | GCAGGAGGATCACCT[A/G]AGCCCAGGAGTTTGA | 11060 |
rs183755427 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69766722 | GATCTTTACTCAACC[A/G]TCACCTTCAGAGAGA | 11060 |
rs183791997 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920272 | AGTTGCTCCAGGGTC[A/G]ACGATCATGCCCCTC | 11060 |
rs183793484 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69892724 | ATTTTCACAGAGACA[A/G]GGTCTCCCTATGTTT | 11060 |
rs183819418 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69935754 | GTCAGGGAAGGAAGG[A/C]GGGTAGCGGTAGCAG | 11060 |
rs183889238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816911 | AGGTGGAGAGATGCT[A/G]TGTAACTTGTCCAAA | 11060 |
rs183897350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814281 | TCCTCTTGCCTCAGC[C/T]TCCAGAGTTGCTGGA | 11060 |
rs183898270 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69901011 | TATTTCAGGAAGGGT[A/C]CTTCGGGGAAGGACT | 11060 |
rs183901982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828265 | CATCCATGCTTAGAG[G/T]CTCCCCTTTCCTGCC | 11060 |
rs183902685 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882008 | TAATTTTTGTATAGA[A/T]GGGGTTTTGCCATGT | 11060 |
rs183909895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852102 | AGAAACTGCTAAACT[A/G]TTTTCCAAAACGGCT | 11060 |
rs183911311 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69861962 | TTCTAGTAATCCTAG[A/G]CAAATACCGCTTACC | 11060 |
rs183929634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69774860 | CTGTAACCCTAGCTA[C/T]TCAGGAGGCTGAGGC | 11060 |
rs183931443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889916 | TCTTTTTTTCACTCC[C/T]TTATCCCATCTCTTT | 11060 |
rs183936129 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69872918 | AAGGAAAAAGAAAAA[A/C]CAAACCCATTCATTT | 11060 |
rs183937847 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69916592 | TGGAAAGTCAGTGGC[A/C]GGGAGACTGAAAAAG | 11060 |
rs183940035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891995 | ACAGGTGTAATTTGC[A/G]TACGATTTATTAAGT | 11060 |
rs183958825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849231 | GCTAGCAGGGAGGAG[A/G]GGTGGAGGGTGGATA | 11060 |
rs183963050 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932071 | GCGGTGGCTCACGCC[C/T]ATAATCCCAGCACTT | 11060 |
rs183963432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907482 | GACAGTACCCAAAAG[A/T]AGAAGTAAATAAATT | 11060 |
rs184067284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830715 | TGTTGGCCTAGCTGG[G/T]TAGAAGAGACTTTCT | 11060 |
rs184095262 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69797758 | GCCAGGCACGGTGGC[A/G]GGCGCCTGTAATCCC | 11060 |
rs184114238 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69876431 | ATGCCGTGGCATGAT[A/C]TTGGCTCACTATAAC | 11060 |
rs184144069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867848 | CCCCTCCCCCTAAAT[G/T]GTGAGGGGGCTTGGG | 11060 |
rs184176291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69904074 | GCCATTGGCGCTCAG[C/T]GCTTTCATTTTTTAA | 11060 |
rs184189624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821894 | TTTTTAAATAAGAAA[C/T]AGGGTCTTACTCTGT | 11060 |
rs184196934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69772180 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGAACTTG | 11060 |
rs184200546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840882 | TGTGATGTAACCATG[A/G]CACTTTCCAGACACC | 11060 |
rs184205282 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69881158 | TTGGTACCCCACTTT[C/T]CCTCCTTGGTACCCC | 11060 |
rs184206362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69861583 | TTGCAGTGACCAGAA[A/G]GGGCCCATTTTAACT | 11060 |
rs184252147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792748 | CTAGGCTAGAGTGCA[C/G]TGGCACAATTACAGC | 11060 |
rs184253814 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69813839 | TTCAAGCTTGCTGCT[C/G]TATCTTTTCACATGT | 11060 |
rs184260221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828119 | GGATGGGCCTTGCCT[A/G]TAGAGCACTGGGACC | 11060 |
rs184278332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69885799 | AACTTGTGGGGTTGC[A/G]TGTGAGGCCTAAATG | 11060 |
rs184291299 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844750 | GGTACCTTCCGATAG[A/T]GTAAGCCTTATCGGA | 11060 |
rs184296133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782208 | GAATCTCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 11060 |
rs184307947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803636 | AAAGGAAGGCAGGGC[A/G]CAGTGACTTACACAT | 11060 |
rs184311709 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69922938 | TCTGTTGCCCAGGTT[A/G]GAGTGCAGTGGCGCA | 11060 |
rs184366264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69917501 | TTCCCCAGAACCACA[C/T]GGATCCCCAAATTAG | 11060 |
rs184391283 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932759 | ATGTCACCCTAAAAA[C/G]AGTCCAAAGCATTGT | 11060 |
rs184397119 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908109 | AAATAGCTGGGCATC[A/G]TAATGTGTGCCTGTA | 11060 |
rs184425084 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69776604 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 11060 |
rs184436857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800079 | AGAGTTGCGTCCCAG[C/T]GAGCGTGTTACATGA | 11060 |
rs184469571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775951 | CTTCAAATTCCTCTA[C/G]TGTCCTTGTTTCTGT | 11060 |
rs184471255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69903688 | CAGGGGAATCGGTTG[A/G]ACCCAGGAGGTGGAG | 11060 |
rs184477909 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69885085 | CACACACACACCACT[C/T]TTTTACAAACTCCTC | 11060 |
rs184493383 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772908 | TCGACACACTGGAAC[C/G]ATTTTCCAAAATTTT | 11060 |
rs184500987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69833633 | TTACTTAGAACAGAA[A/G]GGTGCAGTCGTATAG | 11060 |
rs184511685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921575 | TGTTTCCCTTTCCCA[A/C]CTCCTAGTGTGCTAA | 11060 |
rs184513875 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69878689 | TGGTTTCATGTATCT[A/G]TGTGCTCTTCTTTGC | 11060 |
rs184534798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882538 | AAAAGAAGTTGAAAC[C/T]ACACATCAGCAAAGT | 11060 |
rs184547498 | snp | C/T | 0.000495136 | 0.0157265 | missense | WWP2 | GRCh38.p7 | 16:69842077 | GTAGCTCCAGAGAAC[C/T]GGCACCAGCCCCCCA | 11060 |
rs184580550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69794139 | GCCAGGCTGGTTTCA[A/G]ACTCCTGGTCTCAAG | 11060 |
rs184639070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69862253 | TATTTTTAGTAGACA[C/T]GGGATTTCTCCATGT | 11060 |
rs184660080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901124 | GACAGATTGCTGACT[C/T]ATAAAACAGCCTGAA | 11060 |
rs184737334 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901576 | TACCACCACGCCCAG[A/C]TAATTTTTTTGTATT | 11060 |
rs184814547 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69886588 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 11060 |
rs184820670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937795 | AGGAGACGATAGACC[A/G]GCCTTGGGATGAACG | 11060 |
rs184827762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69868966 | AATCTCGGCTCACTG[C/T]GACCTCCACCTCCCG | 11060 |
rs184829437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69848220 | CTTTGGGAGGCTGAG[G/T]TGAGTGGATCACCTG | 11060 |
rs184840125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845486 | TTAGCTTTTGCTGTC[C/T]GAAGGGTAGGTTTTT | 11060 |
rs184845067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924516 | AACACCCCCCTTCCC[C/T]GCAGGATATGAGAAT | 11060 |
rs184862890 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69904813 | CTCATCAGTCAGAGC[C/G]TTGAGCAAGAATGCC | 11060 |
rs184867155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69783766 | GTCTGGGCAACGTAG[C/T]GAGACCTTGTTTCTA | 11060 |
rs184890648 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69769264 | GGAGGTTTGCAGTGA[G/T]CCGAGATTGCACCAC | 11060 |
rs184896475 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69790903 | CTTATATATTTAAGG[A/G]CGGTTGTATTTCCTT | 11060 |
rs184905291 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WWP2 | GRCh38.p7 | 16:69856666 | GTAGTCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 11060 |
rs184905463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812870 | GCAAAATTACTGTTT[C/T]CCCTTGTCAATGAAA | 11060 |
rs184938248 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69894294 | CTCTGTTGCCCATGC[A/G]GATCTCAAACTCCTG | 11060 |
rs184939145 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805111 | GTGGCATGATCTTGG[A/C]TCACTGCAATCTCCA | 11060 |
rs184949113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69841714 | TTGTTCTCTATCTCA[C/T]GTTTTTGAGGCTCAG | 11060 |
rs184950375 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69878942 | AAGTAGTATAAAATA[C/T]TCATAAAGTGGTATA | 11060 |
rs184959690 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760834 | ATGTTCTTGGAGGCC[A/G]GGCGCATTGGCTCAC | 11060 |
rs184960442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826863 | AGAATGGTGTGAACC[C/T]GGTAGGCGGAGCTTG | 11060 |
rs184965256 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69788515 | ATACACTGGGCAGGC[A/G]TCTGCCTCTGGGCCT | 11060 |
rs184969614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69811831 | GTCGTCCTTCACCCA[A/G]CTGTTAAAATTTGCT | 11060 |
rs184971618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846856 | TCATGTTGTTTCTTT[A/G]CCTGGGTGGTGGCTC | 11060 |
rs184975094 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69828796 | AATATGGGAGTTTCC[C/T]ATTATTCCATCCTCT | 11060 |
rs184980778 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69825153 | ATACTGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 11060 |
rs185001968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873532 | CCCCTGTGCCACCCA[C/G]TGTATCCTTGTGCTG | 11060 |
rs185006732 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69795854 | GGTTTAGCCATGTTG[C/T]CCAGGCTGGTCTCAA | 11060 |
rs185008661 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900394 | GCACTTTTGGGAGGC[C/T]GAAGCAGGAAGATTG | 11060 |
rs185084317 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909046 | GAATTATTAGAAGAT[C/T]TCTGGGAAACAAAAG | 11060 |
rs185088509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891427 | TTGCAGAATGCCTTT[A/G]TCTTTTATGAGGATA | 11060 |
rs185092689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850168 | AAGGTGGGCAGATCA[C/T]GAGGTCAGGAGATTG | 11060 |
rs185098127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69875913 | CAAATGTTCTTAATG[A/G]CATCTAGAATGGTGA | 11060 |
rs185111570 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69916250 | CCCAGGCTGGAATGT[A/G]GCAGCATAATCATAG | 11060 |
rs185115439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773430 | GTGGTCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs185116995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69934625 | TCACGGCATTTGGGA[A/G]TGTCCCACTGAGACA | 11060 |
rs185129748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814903 | ACCTTGGAACTTGAG[C/T]CAGTGGGAGAAGAGA | 11060 |
rs185152581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69890811 | TTATTCTAAGTCTGG[C/T]AGATCGAGCAGCCCA | 11060 |
rs185233981 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69830260 | ATGCCCGGCCTAGTT[G/T]TTTTCTGTTTTATAG | 11060 |
rs185240080 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851698 | TAAAAGTTTTCAACT[C/T]GGTCGGGAACGGTGG | 11060 |
rs185272969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69809345 | CAAATCTTCCCAAAG[A/G]TGGGGAGGTTTGAAT | 11060 |
rs185287856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844313 | TCTTAAGCTAGAACA[A/G]CGGTGGGCGAGGAAT | 11060 |
rs185298001 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69764647 | TCCTGGGAAAACATT[C/G]TTTCATTCAGTGAAT | 11060 |
rs185306810 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938034 | TTGATTCTTTTATAC[A/G/T]TATGGGTTTTGTTGT | 11060 |
rs185344456 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69911166 | GGGAGCAAGATTGAA[C/T]CACCGATTCACTTAA | 11060 |
rs185395119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69824601 | AATTAATTAATGTTT[A/G]TAACACATGTATTGC | 11060 |
rs185400071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830095 | AAGTAGCTGGGATTA[C/T]AGGCACATGCCACCA | 11060 |
rs185416697 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761177 | AGGCACAGTGGCATT[C/T]GCCTGTAGTCTCAGC | 11060 |
rs185426382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69786730 | TGCTGGAATTACAGA[C/T]GTGAGCGACCATGCC | 11060 |
rs185458053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865819 | AGAAAGATACTGAGT[A/G]CACAGCCTCCGTGGC | 11060 |
rs185474353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69893214 | GACAAGAAGAAGTGT[A/G]TCCTTCCTCTGTCAC | 11060 |
rs185477601 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69893695 | TACAGGCTTGCGCCA[A/C]CACGCCCAGCTAATT | 11060 |
rs185521875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774044 | GGTTTGGTGGTCAGT[A/G]TTGTTTTTTTTTAAT | 11060 |
rs185538047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796843 | TTATCTGTTGTCTTC[C/T]TCCCTTCTGTTCCTT | 11060 |
rs185542598 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815741 | GCAGTGAGCCGAGAT[C/T]GCCCCATTGCACTCC | 11060 |
rs185594651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910470 | CTGGAGTGCAGTGGT[A/G]CAATCTCCAGCTCAC | 11060 |
rs185618233 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69853391 | GTGGGTGTGCAGGCG[A/G]TGAGGCATGGTGTCT | 11060 |
rs185631993 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69883747 | CACCCTGCAAAAACT[C/G]TTAAACAGAAGAGCT | 11060 |
rs185639671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776342 | TAGAGCTAGGAGGGA[A/G]TCTTTCTTGACTCTT | 11060 |
rs185653375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69818604 | GTGTTGCTAAACCCA[A/G]TGGTCACTTCTCAAG | 11060 |
rs185666509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918821 | CTAAAGAGTAACATT[G/T]AAATTTTCTTTTTCC | 11060 |
rs185672472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69902413 | AGATTAATTGCAGTC[A/G]GACGGAGACTGCTTT | 11060 |
rs185740107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832993 | CATGAAGGTGGGACC[A/G]CAGGTGCACGCCACC | 11060 |
rs185763776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877889 | CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCAGGT | 11060 |
rs185769017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834972 | TCTTGTTCCTGTTGA[A/G]TCACTAGAATAGTAG | 11060 |
rs185778994 | snp | C/T | 1.65704e-05 | 0.00287836 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799285 | CGTCTTGAAGAACAA[C/T]GGGGGCAAAAGTACG | 11060 |
rs185789791 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919255 | ACTGTAACCTCCACT[G/T]CCCGGGTTCAAGCAA | 11060 |
rs185799348 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69801242 | TTTTTATATATATAT[A/T]TTTTTTGAGACAGGT | 11060 |
rs185806020 | snp | C/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69870053 | CTAAGAGCCTAGGCT[C/G]TTGACATTAAACTGC | 11060 |
rs185841812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69906103 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGA | 11060 |
rs185895798 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69819581 | TCATTTTAATTTAAT[C/T]TAATTTTCTAGAGAT | 11060 |
rs185902260 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69785011 | GAGGTTGAGGCAGGC[A/G]GATCACTTGAGGTTA | 11060 |
rs185904491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806214 | TCTAGAAAAGATTTT[A/T]AAAAATCTATTATAT | 11060 |
rs185913137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822873 | CAGGCACCGTGGCTC[A/G]CGCCTGCAATCCCAG | 11060 |
rs185927782 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69777628 | TAAAAAAATCTTTTT[A/T]TTTATTATAGTTTGG | 11060 |
rs185953358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882884 | CAGACCGGGTGCGGT[A/G]GCTCATGCCTGTACT | 11060 |
rs185963387 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927236 | GGCTGTGGCTGGGGC[C/T]GGCTCCCCAGGGCTC | 11060 |
rs185971947 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69842424 | GCTTCTAATGATCCT[A/G]TTGCCCAGATAGTGA | 11060 |
rs185976817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887749 | CCTGCTACTCTTTTG[C/T]TGCAATAAATGTAAA | 11060 |
rs185982092 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863433 | GTCCTGAGGTCAGGA[C/G/T]TTCAAGACCAGCCTG | 11060 |
rs185990391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901521 | GGGTTCATGCCATTC[C/T]CCTGCTTCAGCCTCC | 11060 |
rs186095653 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926095 | CTCGCGCTTGGTAGC[C/T]GCCTCTTACCTATCC | 11060 |
rs186104722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816271 | AATTTCATATCATGT[A/G]TATTTTACCACAATT | 11060 |
rs186108270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69905423 | GGAGCCTAGAAATGT[C/G]TGTGGACCCATTACA | 11060 |
rs186126152 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69857841 | TAATTTTTAAATTTT[G/T]TTTTGTAGTGACAGT | 11060 |
rs186141163 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69897224 | CCTCTCGCTTCAGCC[A/T]CTCGAGTACCTGAGA | 11060 |
rs186213195 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69906263 | ATTTTTAGTAGAGAC[A/G]GGGTTTTACTGTGTT | 11060 |
rs186223320 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69888416 | TGCTTGTTCTACATA[A/C/G]ATCTTAAAAAGAATC | 11060 |
rs186252105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802764 | ACCTGCCACCATGCC[C/T]AGCTAATTTTTTTAT | 11060 |
rs186253886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820395 | TAAAGGCATGTGCCA[C/T]TGTGCTTGGCTAATT | 11060 |
rs186256355 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69928645 | CAGGCACGGTGGCTT[A/T]TTGCCTGTAATCCCA | 11060 |
rs186263118 | snp | A/C/G | 0.00319074 | 0.0398324 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837758 | CACGCTTCCAATAGC[A/C/G]GTGTGTGTCCTGGAG | 11060 |
rs186268464 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69864778 | CCAGGCTGGAGTGCA[A/G]TGGCTCGATTTTTAA | 11060 |
rs186276607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822648 | AGGAATCGTCTAGAG[G/T]AACAAGAGAAAATCA | 11060 |
rs186277368 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69785269 | AAGGTAGTAGAGATG[A/C]TGGAAGGAGGGAGGA | 11060 |
rs186283378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779700 | TTGAGTTGCCTTAGG[A/G]AAGAAAGAGTCCCAA | 11060 |
rs186291818 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69797669 | CAAGGTAGGCAGATC[A/G]TCTGAGGTCAGGAGT | 11060 |
rs186299445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891285 | TTATTAATTTACCCC[A/T]GGTGTTCCAGAGTCA | 11060 |
rs186323643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933028 | CCTTTTTTCCGTGGT[A/G]ACCTCCTCTCCAGGC | 11060 |
rs186382179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801571 | AGATGGGATCTCCCT[A/G]TATTGCTCAGGCTGG | 11060 |
rs186386440 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | WWP2 | GRCh38.p7 | 16:69935130 | TGGGAGGCACAGCGC[A/C/G]GGAGCCACATGCATA | 11060 |
rs186421070 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69843074 | GGTTATTGGATAAAA[A/G]GAACTGTTGAACAGG | 11060 |
rs186443355 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69908320 | CCTGGAGGGCCTATA[C/G]ATGATCTTGTGGAGG | 11060 |
rs186455432 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69807803 | ACAAAAAAGAAATTT[A/T]AAAAAATTAGCCAGG | 11060 |
rs186462124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69875353 | AAGGTCTCTCCTCGA[C/T]GTTGATGGCTGCTGA | 11060 |
rs186486764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779110 | GCCCGCCACCACACC[C/T]GGCTAATTTGTTATA | 11060 |
rs186588339 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | WWP2 | GRCh38.p7 | 16:69762508 | GGCGTCGGGGGGCGG[C/T]GGCTTCCTGTGGGAG | 11060 |
rs186623289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762818 | GGAAAAAGATGCTGC[A/C]TGGACCCCCTCTGAG | 11060 |
rs186639337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876526 | TCTGCTACCACATCC[C/G]GCTAATTTTTGTATT | 11060 |
rs186639482 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831710 | CCCCAAACAGCTTGA[C/G]TGATGTGTCTTCTAC | 11060 |
rs186653729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793032 | CAATTGTAATCACCC[A/G]GTGGGTTCTTCTTGC | 11060 |
rs186656665 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813878 | TATATTTTTGTCCCA[A/G]CATAATCCAATATAG | 11060 |
rs186665891 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828189 | CCGTTATGTACTGAA[A/G]TGAGGACATGAGTGC | 11060 |
rs186670534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880531 | ATCTGTATATACACC[A/G]GGGAAGGATTTTACC | 11060 |
rs186678234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69772640 | GTTAAGGAGTGGGCT[A/G]TTAGACATTTCTAGA | 11060 |
rs186678691 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69823628 | GTGTACCACCACACC[C/T]AGCTAATTTTTATAT | 11060 |
rs186780785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887323 | AAGAAGGTGCTAGTC[A/T]TGTCTAGCAAACAAA | 11060 |
rs186794704 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69785840 | TCATTATGGCCAGGC[C/T]GGTCTTGAACTCCTG | 11060 |
rs186794799 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763048 | GAACGGGCCATCATC[A/G]AGGCTTTAAAAAACA | 11060 |
rs186799157 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913323 | CAGGCGTGAGCCACC[A/T]CGCCCAGCCAAAAAA | 11060 |
rs186804322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852879 | CTACTTTCATGCTAC[A/G]ATGGTATGTTAAGTA | 11060 |
rs186806480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808261 | ACCTTTTTTTGCATG[G/T]GTCAATAGTCTTTTT | 11060 |
rs186820590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877806 | ATTAAATTTGCTTTT[A/T]ATTTATTTATTTATT | 11060 |
rs186828194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852197 | TTGATGTAGTCCATT[G/T]TCTGGATTTTGGCTA | 11060 |
rs186838634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921739 | GACGGGACTATCACA[C/T]GGCCGACAATTTCTG | 11060 |
rs186840054 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69937047 | GCGCGGTAACGGCCA[C/T]GCGGCCTGGCCGGGA | 11060 |
rs186850648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69892104 | CCTAGCACATATGCA[C/T]CTAGCCTGGCACATA | 11060 |
rs186857197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910117 | GCTAACTCCCGATCT[A/G]TAACCCCCAACCTAT | 11060 |
rs186859296 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918210 | CTGACTTGCTTTGAC[G/T]TCTCCCATCCCTCAC | 11060 |
rs186861069 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69893063 | TGCATCACCCTCTCT[C/G]CGGACTTAGGATCCT | 11060 |
rs186894938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768674 | CCTGACCTAGGGCCC[A/G]TCCTCTTCCTCAAGT | 11060 |
rs186939545 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69846007 | GTGAGCTGAGATCTA[A/G]CCACTGCACTCCAGC | 11060 |
rs186968240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812387 | CCAGGCTGGTCTTGA[C/T]CTCTTGACCTCAGGT | 11060 |
rs186988735 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69903690 | GGGGAATCGGTTGAA[C/T]CCAGGAGGTGGAGGT | 11060 |
rs187072361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798227 | GAGGAATACTCAAGA[A/G]AGGCATGCAGATGTA | 11060 |
rs187087832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817492 | TGACATCAAGTGATC[C/T]ACCCACCTTGGCCTC | 11060 |
rs187092548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69832269 | ACATGCCATTACCCA[A/G]TTCAGTAGCCATCTA | 11060 |
rs187098372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857544 | TCATTGACTGGCTCC[C/T]GGCCTGAAGGTTTTC | 11060 |
rs187108240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69775902 | TAAGAGTTGGTCTGT[A/G]TTTAATGATTGCTGT | 11060 |
rs187122832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877389 | AGGGTTCGGGTCTTG[C/T]TCCAGATTAGGCTTT | 11060 |
rs187124895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895677 | AGGCAGGAGGATCGC[A/G]TAAGTCCCGGAAGTC | 11060 |
rs187127171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826319 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 11060 |
rs187128197 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820182 | AGGATGCAGTGAACT[G/T]TGATCATGCCACTGT | 11060 |
rs187137218 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852526 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs187148786 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940038 | TTGGGAGGCCCCCGT[A/G]GATGTGGCCCTGTGT | 11060 |
rs187155324 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869430 | CTCACTCTTTTGCCA[C/T]GCTCTCAGGCTGAAG | 11060 |
rs187157209 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69789118 | GCTGGACTGCAGTGG[C/T]GCTGTCTCGGCTCAC | 11060 |
rs187252938 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69823962 | TGTAGCATTCAGGCC[C/G]TAAATGAACACCTGC | 11060 |
rs187260178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843812 | AGTTTGAGGCTGCAC[A/T]GAGCTAGCATCAGGG | 11060 |
rs187264153 | snp | G/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941816 | CTCACAGACCCTCCA[G/T]GCCTGGATAGGGGTG | 11060 |
rs187267168 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69913680 | GCATCTGTGCAACAA[C/G]AACAGGAGGCCATGA | 11060 |
rs187280223 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69872760 | ATGGGGGCCCCATTT[A/G]AGAGGAGACAGTGCC | 11060 |
rs187283540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808947 | TTTAGTAGACACCAT[C/T]AGTTTTCTAGTGTTG | 11060 |
rs187285963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899372 | AACAACACAAATTTT[A/G]TACACATTCCACATT | 11060 |
rs187292470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848636 | AGCTAGATGCTGTTG[C/G]TAAAAAAAAAAAAAA | 11060 |
rs187328010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909265 | GGTTCCCTGTCTGCC[A/G]GGGACAGAAAGTTCT | 11060 |
rs187328902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69879208 | ATTTTTAAAAATTGT[A/G]GTGAAAAACACATAA | 11060 |
rs187335032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836022 | TGGCCAGGCTGATCT[C/T]GAACTCCTGGGCTCA | 11060 |
rs187363538 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69912571 | TTGGAGGGTAGTTTT[G/T]TTTGTTTGTTTGTTT | 11060 |
rs187373234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69775402 | GTGTCATGTTTTGGG[A/G]TAAGGTATCTTAAAC | 11060 |
rs187396913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861767 | TTTCTTTTCCCATTA[C/T]GGCTTCCTTTTTTAT | 11060 |
rs187426283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916440 | AAGTTTTTGAGCAGG[A/G]GTGTGACCGAAGGGC | 11060 |
rs187431089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69900621 | TCCGCCTCCTGGACT[C/T]AAGCGATTCTCCTGC | 11060 |
rs187435556 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881420 | GAGCTAATAAAAGTA[A/C]ACTTGCTAAAGGCAA | 11060 |
rs187481369 | snp | G/T | 0 | 0 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838740 | ACTACAAGTGTTATT[G/T]TATAGAAACGTTTAG | 11060 |
rs187505952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803208 | TACTTTTTTGCTCTG[A/C]TCTCCTGGCCTCTCA | 11060 |
rs187565404 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768471 | AAAAATTAGCTAGGC[A/G]TGGTGGCAGACACCT | 11060 |
rs187617278 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69919581 | TCCACCTGCTGGAGT[C/T]TCCATCCCATTAGAG | 11060 |
rs187621872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776137 | GTCTTTTAGTGGGCC[C/T]GTGTCCCAGGCTATG | 11060 |
rs187625464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843284 | ATTATACTTGTTATA[A/C]GTATTACAAATGACG | 11060 |
rs187628362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817947 | TTTTTCCCTACAGTA[A/C]ATTCCCAGGCATGCA | 11060 |
rs187634646 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69884138 | GTATGTATATATATT[C/T]CTTGAAAAAACACAC | 11060 |
rs187661604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771324 | GCTATCTTGGCTCAC[G/T]GCAACCTCCGCCTCC | 11060 |
rs187679675 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69782005 | TAAATTTTCGGAGCC[A/G]GGCGAGGTGGCTCAT | 11060 |
rs187679915 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69827266 | GGTTCATTTATTTCT[G/T]TGCCCCTTTGTATAC | 11060 |
rs187680794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803585 | TCCACCCTGCTTTTT[G/T]GTGTGTGTGTGTGAA | 11060 |
rs187685072 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69847441 | TGAGATGGAGTTTCA[C/T]TCTTGTTGCCCAGGG | 11060 |
rs187736399 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69870204 | AGAACATATATGTAA[A/G]TGCATAGCACACACA | 11060 |
rs187740652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69821837 | AGCTGGGATTATAGG[C/T]GTGAGCCACCATGCC | 11060 |
rs187740841 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859861 | AGACTGAGAGAGCAC[C/T]GCCCCCCACCCCCGC | 11060 |
rs187750952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69780081 | CCCCACTCCAATTCC[C/T]CTGCTCCCTCCTCCC | 11060 |
rs187768417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821192 | ATCCTGCACCTCAGG[C/T]AGATATGCCCAGGCC | 11060 |
rs187863500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69903143 | GGACAATAATAGTCC[C/T]TGAAAGAGAGACTTT | 11060 |
rs187867081 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69832663 | TTCTTGTGCCTCAGC[C/T]TCCCAAGTTAGCTGG | 11060 |
rs187871753 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69884719 | AACAAAATGAAACCT[C/G]ATTGTTCATTTTTAG | 11060 |
rs187879991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865736 | CCCTTGTTGCCCTTT[A/G]AGATGGACACTTAAT | 11060 |
rs187898082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798998 | TTGAGCTCATAGAGC[A/G]TTCATTATTATCTAG | 11060 |
rs187898937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69920563 | TTGACTTAGAGACAA[A/G]GACGTATTTTAGGAG | 11060 |
rs187900125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902839 | CAGGAGGCTCGTCTG[A/G]TTGGTGATAGAATCC | 11060 |
rs187910889 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69865313 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 11060 |
rs187934528 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69892926 | TTGGGGATAAATTCC[C/G]AAATCCTTAATAAGG | 11060 |
rs187965095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935761 | AAGGAAGGCGGGTAG[C/T]GGTAGCAGAGTTTGA | 11060 |
rs187970981 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824630 | GCATGAATTCATTCT[C/T]TTGGAGGGAGGAATC | 11060 |
rs187974616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866103 | TTTCTCTGGCGTCTT[C/G]TTGGCCAAGAGGGGG | 11060 |
rs188070653 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939579 | GGCATCTGATCTACC[A/G]GGTTTTACATATGAA | 11060 |
rs188074707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912017 | AACCTTGGCTGGGCT[C/T]GGTTGCTCACGCCTG | 11060 |
rs188236890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894367 | ATTCCAGGCATGAGC[C/T]ACCGCACCTGGCTGC | 11060 |
rs188239119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69809746 | GGATGCCAGCCTGGG[C/T]GACAAGAGTGAAACT | 11060 |
rs188244826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69879125 | CATAGTATTTGATCA[C/T]TTGTCCTTCCGAGAT | 11060 |
rs188251827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885708 | GTGAATTAGGTGCTA[A/T]ATGACCTTGAGAGGT | 11060 |
rs188253437 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69764290 | CTGTAACCTTGACCT[G/T]CCTGGGCTCGGGTGA | 11060 |
rs188253932 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909458 | CTCTTAGGAGAGCCC[A/G]TGTGCCCTGTTTGGT | 11060 |
rs188257425 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69797771 | GCGGGCGCCTGTAAT[C/G]CCAGCTACTCAGGAG | 11060 |
rs188259973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844421 | TTGGTGCTAGTAACT[A/G]CATCTTAGTCTTTTA | 11060 |
rs188292184 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | WWP2 | GRCh38.p7 | 16:69788188 | AGCAACAGAGCAAGA[A/C]CCCCGTCTCTAAAAA | 11060 |
rs188296618 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811063 | CCCGGCTGGAATTTT[C/T]AAACATAATTTTCAT | 11060 |
rs188302005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824853 | TTGGCTCACTGCAGC[C/T]TCCACCTCCCGGGTT | 11060 |
rs188350200 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911687 | AAGTGGAAATTCACC[A/G]CAGCAGAGTACTTTT | 11060 |
rs188359346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69845004 | ATGCTTATGACTGTA[A/G]GCGGTGGCCAAGGAG | 11060 |
rs188360438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69893767 | CAGGCTGTGCTCGAA[C/T]GCCTGACCTCAAGTG | 11060 |
rs188366213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69889481 | GAATCCCCCCACCAT[A/G]TGACCTTGGCCGAAT | 11060 |
rs188371257 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69878855 | TTCTTAAGACAAAGG[A/G]TGTGAATTTTAAAAA | 11060 |
rs188396850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69931044 | TCCTCACCTTACATT[A/G]CTAATCTTTAAATTA | 11060 |
rs188408452 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69888912 | GGTTTCGCCCTGTTG[G/T]CCAGGCTGGTCTCGA | 11060 |
rs188412300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813649 | ATTTTTTGTATTTTT[A/G]TAGAGACAGGGTTTC | 11060 |
rs188425572 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848103 | ATTTGCTTTTTGATT[C/G]ATAAAATTTTTCATT | 11060 |
rs188496426 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819242 | TGTCTTCCTATGGAA[C/T]GGTTCTGAATGCAGC | 11060 |
rs188506636 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69833784 | AATTGAATCAGACTT[C/T]CTCTAGCCATGCTCT | 11060 |
rs188516835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856069 | TTGAGTCCAGGAGTT[C/T]GAGTCTAGCCTGGGC | 11060 |
rs188525090 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69776836 | TCCATCTCGAAAAAA[A/T]AAAAATAAAAAAAAT | 11060 |
rs188545339 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800567 | ATAGTTATTGTTTTT[C/T]CTTTTTTTTTTTTTT | 11060 |
rs188550765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817190 | CTTGATTTTTTCACC[C/T]AGTTTTTTCCGCATC | 11060 |
rs188553166 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69786428 | ACAGGCATGAGCCAC[C/T]GCGCCCAGCCAATCT | 11060 |
rs188660843 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69851205 | GTATTTTTAGTAGAG[A/G]TGAGGTTTCCCCATG | 11060 |
rs188673158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901015 | TCAGGAAGGGTCCTT[C/T]GGGGAAGGACTGAGT | 11060 |
rs188696682 | snp | A/G | 0.00187231 | 0.0305393 | intron-variant | WWP2 | GRCh38.p7 | 16:69827923 | ATTAAAATATGCTAC[A/G]GCTTGAGAGATTTAC | 11060 |
rs188701418 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69872288 | GTGGCGTGATCTCGG[C/T]TCACTGCAAGCTCCG | 11060 |
rs188707244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891324 | ATGAGAGAAGGAAAT[C/T]TGTCATTTCTAATTC | 11060 |
rs188713840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791507 | TGCTGGGATTACAGG[C/T]GTAAGCCACTGCACC | 11060 |
rs188717544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875489 | CTCTGTAGCATGCGA[C/T]GCTGTTTGACAGCAT | 11060 |
rs188718399 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69916593 | GGAAAGTCAGTGGCA[C/G]GGAGACTGAAAAAGC | 11060 |
rs188731678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69906362 | CAGGTGTCAGCCACC[A/G]CACCCGGCCTTACGT | 11060 |
rs188762699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69899865 | AGATTTGATGAAAAA[C/T]AATATATAATTTCTA | 11060 |
rs188766829 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860926 | GTCCTTTCTGGTCTG[C/G]AGCTATAGTAAAAGG | 11060 |
rs188804481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776485 | AATGAATGAATGCCT[C/T]TTATCTAAGCTCTAG | 11060 |
rs188808554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799670 | AGCCCTAAAACAGAA[A/C]AAAGGAGCTGTGTGT | 11060 |
rs188829391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792215 | ATCGAGGCCCTTAAA[C/T]GTAGGACAGCTATTT | 11060 |
rs188940688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69821897 | TTAAATAAGAAACAG[A/G]GTCTTACTCTGTCAC | 11060 |
rs188944925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796241 | AGTTTCAGGAAAAAG[C/T]GTGTATGTGTATGAG | 11060 |
rs188947020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773876 | AGCACTCCTTTTAGT[A/G]CAGTCACATTAGTTG | 11060 |
rs188951418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841174 | TCTCCACTGCTTCAG[A/G]TTTACAGTCTCCTTG | 11060 |
rs188961566 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813082 | CGTTTTCATGTATGC[C/G/T]TGTGTGTAGGTATGT | 11060 |
rs188981780 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770568 | GCAAATAAAGTGTTT[C/T]CTTGAGTCCTGTGAG | 11060 |
rs189027107 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761034 | GGAGAATTGCTTGAA[C/T]CTGGGAGGCAGAGGT | 11060 |
rs189033552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914461 | CCTTCACAATTCCGA[C/T]GGAAAATGATTTCCT | 11060 |
rs189041230 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | WWP2 | GRCh38.p7 | 16:69840164 | AACCTGCAGACGGAG[A/G]ACAAAGGCAGCGTTG | 11060 |
rs189053703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880884 | GTCCTGAGTGTCCAC[A/C]ACGAGTCTGTGATAC | 11060 |
rs189190035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777803 | CAAGTGTGGTGGCTC[A/G]TGCTTGTAATCCCAT | 11060 |
rs189221440 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69857131 | TTTTTTGAGACAGAG[G/T]CTCACTCTGTCGCTC | 11060 |
rs189225727 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69885956 | ATATGATTAGCTAGA[A/G]GAGGCAGTAGATGAT | 11060 |
rs189227140 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69937850 | CCAGTGGATGTGACA[G/T]GAGGTCGTCAGTGGT | 11060 |
rs189259023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819746 | TTCAGGGATTTTAAA[A/G]TGATTTTTAAAAATC | 11060 |
rs189263166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923000 | GTTTAAGCGATTATC[C/T]TGCCTCAGCCTACTG | 11060 |
rs189280617 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932244 | TGAGGCGGGAGAATC[A/G]CTTGAACCTGGGAGG | 11060 |
rs189288630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907587 | TGCATCCTTTATATA[A/T]AGGTTACTATATTCT | 11060 |
rs189320219 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | WWP2 | GRCh38.p7 | 16:69783771 | GGCAACGTAGTGAGA[A/C]CTTGTTTCTACAACA | 11060 |
rs189411946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905480 | CCCCAAATCCAGAAC[C/T]TTTTGAGTTCCGACA | 11060 |
rs189420232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938662 | CATTCACAGTGTTGT[A/G]CACCTGGCACCACTA | 11060 |
rs189427015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69805861 | ATATCTATTAAGCAG[C/T]CATTGGAATGATTAT | 11060 |
rs189429050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822676 | TCATTTTAGGTGGAG[A/G]GAACAGCATGTGGGA | 11060 |
rs189439015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842185 | ATTGAAAACATGTTG[A/G]GACATGGCGGGGAAC | 11060 |
rs189450156 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69873031 | GGATGTAGATGTTTC[A/G]CTTGGATGAATTGTA | 11060 |
rs189460809 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762089 | AAAATGGGGCTAGTA[C/T]CTGTCCCTGCCTCTA | 11060 |
rs189462709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784664 | TTTTTAATATTCTGT[A/G]TGCTGAAATGGGCAG | 11060 |
rs189476749 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801474 | TCCTGAGCTCAAGTG[A/G]TCCGCCTGCCTTGGC | 11060 |
rs189494012 | snp | A/G | 0.000231424 | 0.0107545 | utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69787002 | GTCTTACAGCTTCAC[A/G]GTGATGATATGGCAT | 11060 |
rs189549643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835001 | AGGTGCTCAAGGCAC[A/G]GATGTGAACAGCACG | 11060 |
rs189555623 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69904219 | AGAATTGCTGTGAAG[A/C]TACAGTATGTCGGCT | 11060 |
rs189568292 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69845665 | TCTGAGGGGTTCATT[C/T]GTCCAAGCTCATCCC | 11060 |
rs189588664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886717 | TTGAGCCAAGATGGC[A/G]CCATTCCACTCCAGC | 11060 |
rs189598783 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69869034 | GCTGGGATTATAAGC[A/G]CTCACCACCATGCCT | 11060 |
rs189613100 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69825836 | CTCCCTATGTTGCCC[A/G]GGCTGGTCTCAAACT | 11060 |
rs189619578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925043 | GTGGTGATTTCAGTC[A/G]CCTTGGCCGCCTTGA | 11060 |
rs189622373 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904829 | TTGAGCAAGAATGCC[C/T]GGGAGAGAAAACATC | 11060 |
rs189679717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69926601 | GCAGGGTACCACTTA[A/G]TCAATGAGCACTGCA | 11060 |
rs189722434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69805316 | GCTGGGATTACAGAC[A/G]TGAGTCACTGCGCCC | 11060 |
rs189729688 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69882110 | CAGGCATGAGCCACC[A/G]CGCCCAGCCTAAGTT | 11060 |
rs189736746 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69841808 | AAGAGAAGCTGTTTC[C/G]AAGGTTTGAGCCCCA | 11060 |
rs189745121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908385 | TTGTCCTAAGTGCAT[C/T]TTGAAGGGAAAGGGT | 11060 |
rs189752856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69765253 | TTTTGTCTTTTTTTT[C/T]CCCACTTAACCTTGA | 11060 |
rs189769761 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69827076 | GGAAGTATTTGCAAG[A/C]AAATCTCATGCCTTG | 11060 |
rs189778106 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69847147 | TGGAGTGCAGTGCCA[C/G]GATCTCGGCTCACTA | 11060 |
rs189778166 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941880 | TGTGTGTCATGGACC[A/G]AGGCAGCCCCCGACT | 11060 |
rs189784527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69914050 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 11060 |
rs189787886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870111 | CTTACTTTCTGTAGA[A/G]CTTCTCTGTGTCTGT | 11060 |
rs189798823 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69770240 | GGGGGCCAGTGGCCA[C/G]GGAAACCAGCCTTGT | 11060 |
rs189802875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791129 | ATTAGCAAGTCTAGG[A/T]CAAAGCAGAAGTTGG | 11060 |
rs189806781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69812901 | AGGTATTATAATTTA[C/T]GGGGAGGTACTTTGA | 11060 |
rs189857952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768566 | AGTGAGCCGAGATTG[C/T]ATCACTGCCCTCTAG | 11060 |
rs189947724 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | WWP2 | GRCh38.p7 | 16:69861963 | TCTAGTAATCCTAGG[A/C]AAATACCGCTTACCC | 11060 |
rs189979968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822352 | AATTCCGAGCTAGAG[G/T]CTGGCGCTGAAGTGG | 11060 |
rs190011229 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69815184 | ATTTTTGTATTTTTA[G/T]TAGAGACAGGGTTTC | 11060 |
rs190030426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782875 | AAGGTCTCACTATGT[G/T]GCCCAGGCTGGTCTT | 11060 |
rs190041711 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | WWP2 | GRCh38.p7 | 16:69934034 | TTATTTGAATATGCC[A/G]GAAAGAACAATTACT | 11060 |
rs190050517 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837949 | AATGAAGGCTAGGGC[A/G]CGGTGGCTCACTCCT | 11060 |
rs190056815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858448 | TGGGTCATGTTGCTG[C/G]TTTACGTTCCCTGGC | 11060 |
rs190066157 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932888 | GCTGTGGCCCGCAGC[A/G]ACCTCTCCGCTCGAG | 11060 |
rs190076138 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850890 | CCCCAAACATATATA[C/T]TCTCTTCCCCACTAT | 11060 |
rs190076694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69880412 | AGAGCTAGTTTTGCC[C/T]TTTTTTCCTCCATGA | 11060 |
rs190081028 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69802980 | ACACTTCCAGTCCCA[A/G]GCATTTCAAATAAAT | 11060 |
rs190082685 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69890834 | GCAGCCCAGGGAAGC[C/T]GATTCCCCTCCCTCA | 11060 |
rs190085152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820765 | TCTATGGGGGCAGGC[A/G]TTTTGTGAATTTTGT | 11060 |
rs190097585 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941538 | AGGGTGGGTCAGGGT[A/G]CAAGCTGCTGGTGAG | 11060 |
rs190112300 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69913484 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACCCTGTC | 11060 |
rs190113138 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69818753 | CTCTCATTCAGTCTC[A/C]CTTGCTCGTTTTTCT | 11060 |
rs190120337 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897647 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11060 |
rs190206628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815782 | ACAGAACAAGACTCC[A/G]TCTCGAAAAAAAAAA | 11060 |
rs190214802 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69830202 | TCAGGCGATCTCTCT[G/T]CCTTGGCCTCCCAAA | 11060 |
rs190230929 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774065 | TTTTTTTAATGCTCC[C/G]CAGATAATTCAGATG | 11060 |
rs190234218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901130 | TTGCTGACTCATAAA[A/G]CAGCCTGAAAACATC | 11060 |
rs190243807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797451 | TCTCAAGCCTGTTTT[C/T]TCCTGGGTAAAATGG | 11060 |
rs190246137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762847 | AGAGTCTCTCCCTTC[C/T]TTCCTGTTTGGAAAT | 11060 |
rs190291098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874855 | GGTCTTAGTTTTCTC[A/C]TTTATAAAATTAGGG | 11060 |
rs190318840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69828918 | TTCCCACGTATCTGA[C/T]GACTCTCTTGGTGTT | 11060 |
rs190320851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69908214 | TGTGTCACTGCACTT[C/T]AGCCTGGGCAACAGA | 11060 |
rs190373013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794870 | GAGATAGTAGCCACA[A/G]GCAATTTGTATATAT | 11060 |
rs190382128 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69828427 | GCTGGAGTACAACAG[C/T]GCGATCTCAGCTCAC | 11060 |
rs190428973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69918880 | ATGGAGTCTTGCTCT[A/G]TTGCCCATGCTGGAG | 11060 |
rs190443544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882573 | ACAGCATGTCACAGG[A/G]GCTGTGCGACTGTGT | 11060 |
rs190474472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917978 | CTGCTTAGTGAGCAG[A/G]GAAAACAGCGTCTGG | 11060 |
rs190485647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69877911 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 11060 |
rs190518978 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69833097 | CTCTTGGACTCAAGC[A/C/G]AGCCCCCTGCCTTGG | 11060 |
rs190527446 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69811882 | CTTCTGAGCCATTTT[A/T]GAGTAAATTACAAAC | 11060 |
rs190547809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918429 | GCCTGCCACTTCATT[G/T]TGTTAATAAAGTTTC | 11060 |
rs190553795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772996 | CTTCCTGTCATTTTG[A/G]TGGAGTTTGAGAAGG | 11060 |
rs190560495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69901966 | TAAATAAATAAATAT[A/G]TAAATAGAGAATTTA | 11060 |
rs190624719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814595 | TGTGTGTTTCTTCTC[G/T]TTCCTCGTGTGTCTA | 11060 |
rs190689681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798013 | ATGAGCCGCCACGCC[C/G]GGCCTTAGCTGTTGT | 11060 |
rs190691698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69842631 | AATGGCCTCCACTCT[C/T]CGGCTATATTCATGT | 11060 |
rs190698613 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69863740 | CTCCTCCTTGTACCC[A/G]TCGCTGCTGGCAAGC | 11060 |
rs190699951 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69887933 | CCCAATACATGTAGT[A/G]TAACATTGTAGATAC | 11060 |
rs190701380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823790 | TTTGTTAAAACATCA[C/T]CTTGTCTTCAGAAGA | 11060 |
rs190709611 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69843321 | TATTTACTGAAATTC[A/C/T]CATTTTATACCTGTG | 11060 |
rs190714944 | snp | A/G/T | 0.00398731 | 0.0445001 | intron-variant | WWP2 | GRCh38.p7 | 16:69883383 | TTCTTTCAAGCTTTC[A/G/T]TGTTCTAAGAATGTG | 11060 |
rs190719529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865324 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACC | 11060 |
rs190725065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69899692 | AGATTGTACCACTGC[A/G]CTCCAGCCTGGGTGA | 11060 |
rs190725710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909063 | CTGGGAAACAAAAGG[C/T]GCATGGGAGGCCAAG | 11060 |
rs190729271 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69928566 | ATTTGTTCCCCAGCC[C/G]CACTCCATGAACATT | 11060 |
rs190730797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822906 | CTTTGGGAGGCTGAG[A/G]CCAGTGGATCATTTG | 11060 |
rs190733159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775514 | TTCTGTTGACTCTTA[C/T]AGTTGCTATATCTCT | 11060 |
rs190733831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69891662 | TTCTCCCCCTGGCTC[A/G]ACTCAGCCATTCCCT | 11060 |
rs190740234 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69876300 | GGAATCATGATCTAA[A/G]GCAGTTATAGCCTTA | 11060 |
rs190760876 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69934984 | GTGAGCCAGTTCTGG[A/G]GAGGGGCGTCCCAGC | 11060 |
rs190761548 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69788535 | CCTCTGGGCCTTTGC[A/G]CTTGCTGTTCCCTCT | 11060 |
rs190776017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854043 | AACATCGTATTCCTG[A/G]CAGTGAACCACAGGG | 11060 |
rs190778070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69893424 | TCTTTGATGCCTCAA[A/G]GAAAGAACAGCTATG | 11060 |
rs190805529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898726 | GTTTGTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 11060 |
rs190914609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929394 | AACCTCAGGGAAAGG[A/G]CACCGGCTCTCCGTG | 11060 |
rs190933871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880574 | AGGTAACACAGTATG[A/G]CTTCGTCCATTTTTA | 11060 |
rs190939718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69906111 | GGAGTCTTGCTCTGT[C/T]GCCCAGACTGGAGTG | 11060 |
rs190983128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869485 | AGTACCTGGGACCAC[A/G]GGGGCACGCCACCAC | 11060 |
rs191007281 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69826451 | ATGGTGGGTGCTTGT[A/T]GTCCCAGCTACTTGG | 11060 |
rs191060987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906277 | CAGGGTTTTACTGTG[C/T]TAGCCAGGATGATCT | 11060 |
rs191071699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69888612 | ATTTTATCGTATCAG[C/G]CCACGGAGGAGTTGG | 11060 |
rs191082325 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870628 | GAGAGTAGTTTTATC[A/G]CCCCATGTTGCATGG | 11060 |
rs191082506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847842 | AGGTCTCACCTCCCA[A/G]CTCTGCCACATTGGG | 11060 |
rs191135114 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69801674 | GCCTCAGCCTCCGGA[A/G]TAGCTGGAACCACAG | 11060 |
rs191141644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69789437 | GTTTCACCATATTGG[A/G]CAGGCTGGCTTCAAA | 11060 |
rs191149637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820209 | CTGTACTCCAGCCTG[G/T]GTGACAGAGTGGGAC | 11060 |
rs191182205 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69779182 | TCTCAAACTTCTGAC[C/T]TCAGGTGATCCACCT | 11060 |
rs191257069 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69779826 | CCCAAGGCTCAATTT[A/G]TAATTATTTATAATC | 11060 |
rs191261551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846396 | AACAATACATGTTGT[A/G]TGGATACCTTCAGAG | 11060 |
rs191269642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887498 | GCAAACTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 11060 |
rs191297216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69808025 | TGTGTCCACAGCTGC[A/G]TAATCATCACCCACA | 11060 |
rs191333486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849195 | AGTCCTGGGAGGGCC[A/G]GGGGAGAATTGGGAA | 11060 |
rs191353589 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889687 | CCGGGAGGTGAAGTC[C/T]CTTCTTCGCAGCTCT | 11060 |
rs191355709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69794066 | GGAACTACAGGCGTG[C/T]GCCACCACGCCCGGC | 11060 |
rs191363205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872821 | TGGCTCTGCTTCCCC[A/G]TAAGTGAGACGGGAA | 11060 |
rs191365662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69843219 | CTTTGGGGGTGGCCC[A/G]TGGTTCCCTTGTAAT | 11060 |
rs191369161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69814200 | AGGTCTTGCTCTGTC[A/G]TCTAGGCTGCAGTGC | 11060 |
rs191373001 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69828208 | GGACATGAGTGCCCA[A/G]TCCACCTTCCTTTCT | 11060 |
rs191381804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883860 | GATTTGCAGCTGCAT[A/G]AACAGTCAGATCCGA | 11060 |
rs191386607 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69812413 | CAGGTAACCTGCCCG[C/T]CTCGGCCTCCCAAAG | 11060 |
rs191394519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907059 | CACTACAGTAAATAT[G/T]GCATTTTCTCTTGAG | 11060 |
rs191432492 | snp | A/G | 0.000214343 | 0.0103501 | intron-variant | WWP2 | GRCh38.p7 | 16:69936295 | ACATCTCCCCACTTG[A/G]TCTCCTGTGCCCCCA | 11060 |
rs191487752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892259 | AGTTTCGTTACATAG[A/G]TATACACGTGCCATG | 11060 |
rs191491697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772731 | GTGTCTTGTGGGGAG[A/G]TGCTTTTGGTGCCTC | 11060 |
rs191506807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852398 | TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGT | 11060 |
rs191512195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935344 | CCAGGTCTAGAGACC[C/T]GCCTGGCCCAGCAGC | 11060 |
rs191533562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785366 | ATCTACTACCAAGAG[C/G]TCAATGGCTTCCCAA | 11060 |
rs191544451 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | WWP2 | GRCh38.p7 | 16:69823474 | TTTCTCTTTTTCTTG[G/T]GTTTTTTTTTTTTGA | 11060 |
rs191560313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69900713 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 11060 |
rs191564090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822300 | AGGGGCAGGGCCTGA[C/T]GCTGATTTATCAGCT | 11060 |
rs191567486 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | WWP2 | GRCh38.p7 | 16:69881792 | CCCTTCCTGGGCTCA[A/G]GCGATTCTCCTGCCT | 11060 |
rs191569463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841665 | ATGGAGAAATGCCCC[C/G]GATTTCTGGCCCCTA | 11060 |
rs191578417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861790 | TTTTTTATTTTTTCA[C/T]GCTTCTATTTTAAGT | 11060 |
rs191612256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69902416 | TTAATTGCAGTCAGA[C/T]GGAGACTGCTTTTAA | 11060 |
rs191649181 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69792463 | TCTGTGTATAAAGAT[A/G]TATTTCATGAAAGAG | 11060 |
rs191649417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69772112 | GATTACAGGCACGCA[C/G]CACTACACCTGGCTA | 11060 |
rs191665147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69785026 | GGATCACTTGAGGTT[A/G]GGAGTTCGAGACCAG | 11060 |
rs191750284 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69876644 | GCTGAGATTATAGGC[A/G]TGAGCCACTGTGCCC | 11060 |
rs191793329 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909573 | TTTTCCAGTAGAATG[A/C]TTGAGTTTTCCTTTT | 11060 |
rs191802299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69892989 | ACCCTTCAAGCCTTC[A/G]GTGGGATCCACTCCA | 11060 |
rs191824717 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69830541 | GGGTAGATTCCCAGC[A/G]GTAGTAGCCCAAAGA | 11060 |
rs191845894 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69902968 | GCCAGGTCATGGATC[A/G]GGGAGGACCCGCAGG | 11060 |
rs191887293 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762684 | AGGGGAGAGGAGCTT[A/G]GGTTCCCAGGCATGG | 11060 |
rs191909552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852570 | TGAGCTGCCTTGCCC[A/G]GCCTATGATATGGAG | 11060 |
rs191934320 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69877402 | TGCTCCAGATTAGGC[A/T]TTGGCTTAAGAGAAT | 11060 |
rs191943922 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69797746 | ATACAAAAATTAGCC[A/G]GGCACGGTGGCGGGC | 11060 |
rs191946008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817499 | AAGTGATCCACCCAC[C/G]TTGGCCTCCCAAAGT | 11060 |
rs191947812 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69831815 | GCATGCTGGCATGGA[A/G]AAAAACAAAACCTTT | 11060 |
rs191949095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766348 | GTCTCCCTCTTCCAC[C/T]CTGGCTGGCCTTCAC | 11060 |
rs191949362 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69787134 | CCAGGGAAGAGGGAG[A/G]ATCTAACCACACCTT | 11060 |
rs191951650 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832446 | TGCCAATTTCATACC[C/T]AGAAAACTCAATGGT | 11060 |
rs191963003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69807058 | TTTGAGATGGAGTTT[A/G]TCTCTTTTTGCCCAG | 11060 |
rs191987665 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69865742 | TTGCCCTTTGAGATG[A/G]ACACTTAATATTTAA | 11060 |
rs191995202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833386 | GGGCAGATCTAGAGG[C/T]TGAGACTGACCTTGG | 11060 |
rs192017725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903283 | TGATTTCATTTCTGG[C/T]AGTGTGTGGGAATAC | 11060 |
rs192031205 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69799701 | ATACGTATATGTGTG[C/T]GTGTGCATGCCTGTG | 11060 |
rs192031391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885070 | TAGAAACTCCCCCTA[A/C]ACACACACACCACTC | 11060 |
rs192033471 | snp | A/G/T | 0.00518157 | 0.0506848 | intron-variant | WWP2 | GRCh38.p7 | 16:69844083 | TTGGATCTTTTTTCC[A/G/T]TACCTTTATTAGAAG | 11060 |
rs192037987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818868 | GCACATCCAGCCTCC[G/T]TGCTTTAAATTTGGC | 11060 |
rs192047214 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | WWP2 | GRCh38.p7 | 16:69770685 | TTGATGTCGCAAGTC[A/C/G]GGGGCAGTCTTGGGG | 11060 |
rs192059398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836539 | AATAGAACAGAGGAG[A/G]GTTATGTTCTCAAAA | 11060 |
rs192069469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69920836 | ATTTTTTTTTCCCTT[A/G]AAAGCCCCACTAGTT | 11060 |
rs192097803 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69879312 | ACTATAACCACCAGT[A/G]TCCATTTCCAGAACT | 11060 |
rs192111480 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813450 | TACAGGCGTGAGCCA[C/G]TGCGCCCAGCCTTTT | 11060 |
rs192113407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69816616 | TATTATTTCATGCCT[A/G]TTACTAAAAAGGACA | 11060 |
rs192125778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912795 | CACACCTGTAATAGT[A/T]GAACTTCCAGAGGCC | 11060 |
rs192133518 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69852029 | TTTTAACTTGCTTGG[A/G]TAAATACAAAGGAAC | 11060 |
rs192141706 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69919891 | TTGACCTCCTGGGCT[A/G]AAGTGATCCTCCCAC | 11060 |
rs192156593 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69884621 | TGACAGAGCAAGACC[C/T]TATCTTAAAAACAAA | 11060 |
rs192223057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69916526 | TAATTCTGGGGTAGG[A/G]GCAGTAGTCCAGGGG | 11060 |
rs192257869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860184 | TTAGCCAGGCGTGGT[A/G]GTCCGATTCCATTCT | 11060 |
rs192260158 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69774778 | AGTTCAAGACCAGTC[A/T]GGACAACTTGGTAAA | 11060 |
rs192331020 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785982 | CTTTCCTTTTTTTTT[C/T]TCTTGCATTATACTT | 11060 |
rs192335331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763321 | TGAGAGGTCTGTGTT[A/G]TGTTCCTTAGAACTG | 11060 |
rs192347512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808882 | ATACATTTCTATTGC[A/G]TATGTACAGATCTAG | 11060 |
rs192373695 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69780166 | TTTTATACTTTTAAA[C/T]GTTTGTGTGTCCACA | 11060 |
rs192389907 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69821769 | GTCTCACTGTGTCAG[A/G]CTGGTCTCAAACTCC | 11060 |
rs192419500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937049 | GCGGTAACGGCCACG[C/T]GGCCTGGCCGGGAGC | 11060 |
rs192425010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791525 | AAGCCACTGCACCTG[G/T]CCTCTTTTCTTTTTT | 11060 |
rs192426673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910443 | AGACGGAGTCTCGCT[C/T]TGTTGCCCAGGCTGG | 11060 |
rs192437973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893203 | GATCCCTGGTGGACA[A/G]GAAGAAGTGTGTCCT | 11060 |
rs192456117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69895767 | CCTGTCTCAGTTAAA[A/G]GAAAAAAAAGTTTCT | 11060 |
rs192492610 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | WWP2 | GRCh38.p7 | 16:69857692 | TTTGAGACAGGGTTT[C/T]GCTCTGTCACCCAGG | 11060 |
rs192495025 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940233 | GTCCTCTAGACCCCA[C/T]CCTGGGTGTATGTGA | 11060 |
rs192496752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827537 | TCCAATGTATACAAG[A/G]GAATTTTTTTAAAAG | 11060 |
rs192535777 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760554 | CACCAGGTTGGCCAA[A/G]TGGGTTTCGAACTCC | 11060 |
rs192541099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932456 | ACTGGGTCATGAGGC[A/G]ACGGAGGACTCCTGG | 11060 |
rs192541794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69827944 | AGAGATTTACCAAGA[C/T]GGATGAAATCTTTGT | 11060 |
rs192543168 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803933 | AAAGTAAAGGAATAA[A/T]GAATGGCAGAGCAGC | 11060 |
rs192552136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69907885 | TAAATGAATCTTATA[C/T]TACAAAAATAAATGT | 11060 |
rs192556933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890291 | CGCTACCTAACTCCC[A/G]TCTGTTCAGAAAGTC | 11060 |
rs192585398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872505 | CAGACGTGAGCCACT[G/T]CGCCTAGCCTTTCTA | 11060 |
rs192618233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69906691 | AGAGTTCGAGACCAG[C/T]CTGGGCAAAGCAAGA | 11060 |
rs192655576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821853 | GTGAGCCACCATGCC[C/T]GGCTATTTTTCTTTG | 11060 |
rs192659760 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838862 | TAAGGGAAGGTAGAG[C/T]GCTTAGGAGAGCTTG | 11060 |
rs192660212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840623 | GGTTGAAGGTGTTTT[C/T]ATGAGAGGCATTGGT | 11060 |
rs192686545 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69782094 | TCGAGACCAGCTTGG[A/C]CAACATGGTGAAACC | 11060 |
rs192693525 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69803635 | TAAAGGAAGGCAGGG[C/T]GCAGTGACTTACACA | 11060 |
rs192712266 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69885775 | TAAGTGGGGATATCA[A/G]TTGTAACTAACTTGT | 11060 |
rs192729212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921772 | GCATCTCTCTCTGCA[A/G]TATTGAAACAGATTA | 11060 |
rs192748818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803376 | TTTACATAAAAAAAA[A/C]ATTATCTTACACAAT | 11060 |
rs192762789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775920 | TAATGATTGCTGTAA[C/T]TGTTGGTATCTGAGG | 11060 |
rs192769498 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924228 | TCAGCTGGGGGTGGA[A/G]GGAGGGCTGTGGAAG | 11060 |
rs192780214 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69809763 | ACAAGAGTGAAACTC[A/C/T]GTCAGAAAGAGAAAG | 11060 |
rs192790327 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69844624 | TCATTGGTGTTGAGA[A/C]TGACACCAGGTCATC | 11060 |
rs192820556 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69813677 | TTCACCATGTTGCCC[A/T]AGGCTGGTCTTAAAC | 11060 |
rs192822764 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783072 | CTGGGGTGCAGCGGC[A/G]TGATCTCAGCTCACT | 11060 |
rs192843309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69889083 | CTTTGGGAGGCTGGG[A/G]TGGGAGGATCACTTG | 11060 |
rs192860069 | snp | C/G | 0.00328927 | 0.0404205 | intron-variant | WWP2 | GRCh38.p7 | 16:69930100 | AGAAGGTGGGGCCAG[C/G]CCTTCACCCTTTTCT | 11060 |
rs192862442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854123 | CCAGATCTGTATCTG[G/T]ATTCTACTACTTCTT | 11060 |
rs192872455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69823986 | CACCTGCTGCAGGCC[A/G]GGAATGGTGGCCTTG | 11060 |
rs192885065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893568 | TTTTTTTTGTTTGTT[A/T]GTTTTTGTTTTTGTT | 11060 |
rs192900702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69937856 | GATGTGACAGGAGGT[C/T]GTCAGTGGTCAGCCT | 11060 |
rs192914134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903927 | CTAGTATTAGGGCTT[C/T]TGTGCCACAAAACTA | 11060 |
rs192935077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69786514 | TGCAGTGCAATGGCC[A/G]ATCTTGGCTCACTGC | 11060 |
rs192993774 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824631 | CATGAATTCATTCTC[C/T]TGGAGGGAGGAATCC | 11060 |
rs193005441 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69799062 | ATATATGTGGGTGTC[C/T]GCCTGTTTTGGTTCC | 11060 |
rs193028648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69877852 | TCATGCTGTTGCCCA[C/T]GCTGGAGTGCAATGG | 11060 |
rs193041848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69832964 | GGCTCAAGTGATTCT[C/T]CTGCCTAGCCTCCCA | 11060 |
rs193073552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69809122 | GTTGCTGGCACCAGC[C/T]GTAGCACGTTGTGCA | 11060 |
rs193089547 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69911153 | GACCTAGTCCCTGGG[G/T]AGCAAGATTGAACCA | 11060 |
rs193097376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915306 | AACGGTGAGTTTCCA[C/T]ATTGAGAGGACGAGG | 11060 |
rs193102570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880886 | CCTGAGTGTCCACCA[C/T]GAGTCTGTGATACAC | 11060 |
rs193107126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849544 | CATAGTCCCTGCTCA[A/C]AGTCCCTGCTTGTAG | 11060 |
rs193108796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878202 | ACAGATCTCCATGAC[A/G]GATATAAATAACAAT | 11060 |
rs193167963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764506 | CTGAAAGTTTTATTT[G/T]TACATAATTTTTCAG | 11060 |
rs193206425 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69776260 | GGATAAGGCTCTGGT[A/G]AAGTCTTCTTCCCTG | 11060 |
rs193209772 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69818360 | TTACAGGCACCTGCC[A/C]CCACGCCCAGCTAAT | 11060 |
rs193225964 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853063 | ATTCTTTGGAGACAG[A/G]GAACCAGTGGATTTT | 11060 |
rs193257263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69900090 | ACTGCTGTAATATGA[C/T]GTAACAGATGCACTT | 11060 |
rs193295399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69861453 | AATTGTTTGTCTTCC[A/G]GAAGTCTTTCTGTAA | 11060 |
rs199513055 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929466 | AGAGACAGGACAATG[A/G]ACGGGTGTATTACGT | 11060 |
rs199546786 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854553 | TTTCTTTTTTTTTTT[A/T]AGTTTATTTATTTTT | 11060 |
rs199603927 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855708 | GCAGAAGAATGGCTG[A/C]TGGAAAGGCCTTAAG | 11060 |
rs199621753 | snp | A/G | 2.72773e-05 | 0.00369295 | intron-variant | WWP2 | GRCh38.p7 | 16:69871974 | GCACTGAAGCTGTGG[A/G]CTCTCACCCGTTCTA | 11060 |
rs199673466 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761559 | GCCTGGGCGACAGAG[C/T]GAGGCTCCATCTCAA | 11060 |
rs199673729 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844518 | GCTATTAACAAGTTT[G/T]GATCTAAATTCTTGA | 11060 |
rs199689416 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809801 | GAGACAGAGAGAGAG[A/T]GAGAGAGATAGGAAG | 11060 |
rs199690552 | snp | A/G | 0.000149884 | 0.0086556 | intron-variant | WWP2 | GRCh38.p7 | 16:69936466 | ATGTGAGTCTCAGGC[A/G]CCGGGGGCTCCGCTC | 11060 |
rs199698322 | in-del | -/TCAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929195 | CCTCCCTCCGACCAA[-/TCAA]CCAAAGAAGTGCTTC | 11060 |
rs199721364 | in-del | -/CAAA | 0.046775 | 0.145601 | intron-variant | WWP2 | GRCh38.p7 | 16:69886463 | AAGAAAAAAAAAAAC[-/CAAA]CAAACAACTTTCTGG | 11060 |
rs199723151 | snp | A/G | 4.94295e-05 | 0.00497115 | missense | WWP2 | GRCh38.p7 | 16:69888164 | CTCCCTGCCCCAGCC[A/G]CACCGGCTGAAGGAG | 11060 |
rs199833750 | snp | G/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910008 | TTTTTGGCTGTTTTT[G/T]TACTTCATTGGCAGA | 11060 |
rs199893535 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853365 | CTTGCAACCGCTTTA[-/TG]TGTATTTGAAGTGGG | 11060 |
rs199895251 | snp | C/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925213 | CTCACTTGGGCCCTC[C/T]GTGCGCAGGGTTCTT | 11060 |
rs199900980 | snp | A/G | 0.000494096 | 0.01571 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888130 | CTTGAGTGTGACCCC[A/G]AATCCCAACACGACT | 11060 |
rs199903220 | snp | C/T | 0.0019304 | 0.0310077 | intron-variant | WWP2 | GRCh38.p7 | 16:69871761 | CACTTCTGTCCTTTT[C/T]ACAGTGACTTATGTC | 11060 |
rs199905032 | snp | C/G | 1.65021e-05 | 0.00287241 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908881 | AGAAGACCTGAGACT[C/G]TGGAACTGACACCAT | 11060 |
rs199913689 | in-del | -/ATAT | 0.0520825 | 0.152737 | intron-variant | WWP2 | GRCh38.p7 | 16:69777131 | ACAATACACATATGG[-/ATAT]ATATACACATATGTG | 11060 |
rs199925413 | in-del | -/CTG | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69928165 | TTGCACTTCCCTGTT[-/CTG]CTCCTTTTTCAGCTT | 11060 |
rs199937445 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850403 | AAAAAAAAAAAAAAA[-/T]GATGAAAAGTCAGGG | 11060 |
rs199937557 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881131 | TGCAACTGCCATCTT[A/T]CTGCTTACCATTTGG | 11060 |
rs199942053 | in-del | -/GGGTGTACTACCCAA | 0.0263992 | 0.111815 | intron-variant | WWP2 | GRCh38.p7 | 16:69806077 | TGATGGTGTACGCCT[-/GGGTGTACTACCCAA]GTAGTCCCACCTACT | 11060 |
rs199942217 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874659 | ATGGCATAGCCCTTC[A/T]TTGAGACTTGTATGG | 11060 |
rs199955520 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912306 | CAAAAAAAAACAAAA[A/C]AAAACCTCATTGGTT | 11060 |
rs199965453 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785225 | TAGGTGTGTGAGACT[C/G]TCTCAAAAAAAAAAA | 11060 |
rs199984855 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918274 | TGAGACCCTGTCTCT[-/A]AAAAAAAAACAAAAA | 11060 |
rs199986943 | snp | A/G | 1.65707e-05 | 0.00287838 | intron-variant | WWP2 | GRCh38.p7 | 16:69930088 | CCACCAAGGTCCAGA[A/G]GGTGGGGCCAGCCCT | 11060 |
rs199987561 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851983 | CAGCGAGATTCCAGC[C/T]AAAACAAAACAAAAC | 11060 |
rs199991126 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783806 | CAACAACAACAACAA[A/C]ATATTAGAGTTGTGG | 11060 |
rs200013543 | in-del | -/TCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912702 | AGTCTGCAGCCCTCA[-/TCT]TCTGAGGATACAGAA | 11060 |
rs200023554 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907981 | TGCGGTGGCTCACTC[-/C]TGTAATCCCAGCACT | 11060 |
rs200042965 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805771 | GTGTTACTAATTTAA[-/T]TTTTTTTCTTTTTTT | 11060 |
rs200046595 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869403 | TAATTTTTTTTTTTT[-/G]TTAAACAAGGTCTCA | 11060 |
rs200060090 | snp | C/T | 0.000842022 | 0.0205013 | intron-variant | WWP2 | GRCh38.p7 | 16:69939313 | GGACGTCTCTGCTGA[C/T]GTCGGCGTGTTTTAC | 11060 |
rs200079228 | snp | A/G | 0.000308573 | 0.0124174 | intron-variant | WWP2 | GRCh38.p7 | 16:69917667 | AATTGGGGGATGGGA[A/G]TGGGGTGGTCATTAT | 11060 |
rs200091634 | snp | A/G | 1.9128e-05 | 0.00309251 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842040 | ATCACAGCTGCCTTC[A/G]AGAGACTCCAGTGGA | 11060 |
rs200119284 | snp | G/T | 0.000217582 | 0.010428 | missense | WWP2 | GRCh38.p7 | 16:69935870 | GCTGTACCATGGAAA[G/T]TTCATCGACACGGGC | 11060 |
rs200202528 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923320 | TGTGTGTTGGGGGGG[G/T]GGGGGGGGTGCGTTC | 11060 |
rs200211230 | in-del | -/C | 0.039522 | 0.134904 | intron-variant | WWP2 | GRCh38.p7 | 16:69906848 | TCACACCACCACACT[-/C]CAGCTCGGGCAACAG | 11060 |
rs200212833 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803368 | TTGGAACATTTACAT[-/A]AAAAAAACATTATCT | 11060 |
rs200239359 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919240 | GCATGATCTCAGCTC[A/C]CTGTAACCTCCACTG | 11060 |
rs200239970 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795295 | ACACACACACACACA[C/T]ACACAGAGACATAGA | 11060 |
rs200264806 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885069 | TTAGAAACTCCCCCT[-/AC]ACACACACACCACTC | 11060 |
rs200268272 | in-del | -/GCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763138 | CTTACACTGTTGACC[-/GCT]TAGCCCAGCGTTACC | 11060 |
rs200280946 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859572 | AAAAAAAAGAAAAAG[-/A]AAAAAAAAGTCATTC | 11060 |
rs200311655 | snp | C/T | 8.36058e-05 | 0.00646497 | intron-variant | WWP2 | GRCh38.p7 | 16:69939457 | GGGGGGCCTCAGACC[C/T]GATGAGCTCCTGGGA | 11060 |
rs200322203 | snp | A/G | 6.83399e-05 | 0.00584511 | intron-variant | WWP2 | GRCh38.p7 | 16:69917907 | GCAGGCGCTTGGCCC[A/G]AGGTGGGGCCGCCTC | 11060 |
rs200328802 | in-del | -/AAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860852 | AGTTAAAAAAAAAAA[-/AAG]GAAAGAAAGAACACT | 11060 |
rs200329679 | in-del | -/C | 0.209388 | 0.246679 | intron-variant | WWP2 | GRCh38.p7 | 16:69845909 | CAAAAATTAGCCAGG[-/C]CATGGTGGTGTGTGC | 11060 |
rs200335131 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897106 | CGTCTTTTTTTTTTT[G/T]TTTGTGTGTTTTGTT | 11060 |
rs200339483 | snp | A/G | 6.60698e-05 | 0.00574722 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69930256 | CCCGGGGTTTGAGTC[A/G]GGGTAAGGACTTTGT | 11060 |
rs200358512 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852973 | AGTTTGCCAGTCCCT[G/T]GCTGTAGGAGATGGT | 11060 |
rs200361210 | in-del | -/CCAAAGTGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820502 | ACCCACCTCAGCCTC[-/CCAAAGTGT]TGGGATTACAGGCGT | 11060 |
rs200377558 | in-del | -/TTTGTT | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69893566 | TGTTTTTTTTGTTTG[-/TTTGTT]TTTGTTTTTGTTTTT | 11060 |
rs200391227 | snp | C/G | 0.000115933 | 0.0076127 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931792 | CTGGCCCGATGCTCT[C/G]TCTTCCCAGATCATG | 11060 |
rs200393839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906739 | AAAAAGATTAGCTGG[A/G]CCTCGTGGCATGCAC | 11060 |
rs200393985 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827432 | ATGAATAATTTTCCA[-/TGT]TGTTGTTGTATACGC | 11060 |
rs200402402 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885311 | GTGTTTTACTGGCTT[G/T]CCTGAGATAGAATAG | 11060 |
rs200410817 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847730 | TTTTAATAACCCATT[C/T]TTGCAGGTTCCCAAC | 11060 |
rs200414654 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809805 | CAGAGAGAGAGAGAG[A/T]GAGATAGGAAGGAAG | 11060 |
rs200414886 | in-del | -/CCACTTCCC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785711 | GGCCCACTGCAACCT[-/CCACTTCCC]GAGTTCAAGCGATTC | 11060 |
rs200477944 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836294 | TCCATCCTGCCTCCT[A/G]TTTTTTTTTTGTTTA | 11060 |
rs200523950 | in-del | -/TTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849856 | CATTTATACATTGGT[-/TTA]TTATTTTGCATCAAT | 11060 |
rs200541946 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879462 | TTCTAGATACCTCAT[A/G]TAAGTGGATTAACGT | 11060 |
rs200553752 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821266 | CCTCAGCCCCACACC[A/C]TCAACTTCTCAAAGT | 11060 |
rs200557067 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841697 | TTTGCATGGTTAGGG[G/T]TTTGTTCTCTATCTC | 11060 |
rs200557220 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778961 | TTTATTTATTTATTT[A/T]TTTTTTGAGATGGAG | 11060 |
rs200571247 | in-del | -/GTT | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69812142 | GACATTGGCATCGGC[-/GTT]GTTGAAGAGTACAGA | 11060 |
rs200585482 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69908465 | AATGCTGAATTTTTT[A/T]AAAAAATCCATGGAA | 11060 |
rs200593517 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823718 | AGTGATCTGCCTGCC[C/T]CAGCCTCCCAAAGTG | 11060 |
rs200599616 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834530 | AAAAAATTTTTTTTT[-/AG]TTTTTTTTTTTTTGA | 11060 |
rs200632719 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876351 | TGGGGCATGTTTTTT[-/G]GGGTTTTTTTTTTTT | 11060 |
rs200637120 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851981 | AGCAGCGAGATTCCA[A/G]CTAAAACAAAACAAA | 11060 |
rs200640878 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823139 | TGTCTCAAAAAAGAA[-/G]AAAAGTAAAAACAAA | 11060 |
rs200654237 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801198 | AAAAAAAAAAAAAAA[-/G]CAATTTTACTTTAAT | 11060 |
rs200664584 | snp | A/G | 6.64165e-05 | 0.00576228 | intron-variant | WWP2 | GRCh38.p7 | 16:69937498 | TGCTAGCGAGTGGAC[A/G]ATGCGCGGGGAGGGA | 11060 |
rs200681828 | in-del | -/ATTCATTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806954 | TTTATTTATTTATTT[-/ATTCATTC]ATTCATTCATTCATT | 11060 |
rs200683787 | snp | A/C | 1.64912e-05 | 0.00287147 | missense | WWP2 | GRCh38.p7 | 16:69840258 | ATGGCAGTGCCCTGA[A/C]AGATGGTGAGTGCCG | 11060 |
rs200698191 | snp | A/G | 1.66557e-05 | 0.00288575 | intron-variant | WWP2 | GRCh38.p7 | 16:69929554 | TGGGCTGAGAGGGGG[A/G]CCGGGCTGGGCTGGG | 11060 |
rs200737728 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846071 | AAAAAAAAAAAAAAA[A/G]AATACTTATCTGGTC | 11060 |
rs200790357 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838443 | GGAGACCCTCCTTGA[C/G]TTAAAAAAAAAAAAA | 11060 |
rs200810761 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885102 | TTTACAAACTCCTCC[C/T]ACACACACACACACA | 11060 |
rs200856848 | snp | C/G/T | 0.000808884 | 0.020095 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888232 | GGCTGCCCAGGCCCC[C/G/T]GACGCTCTGCCTGCT | 11060 |
rs200856879 | in-del | -/T | 0.454904 | 0.143228 | intron-variant | WWP2 | GRCh38.p7 | 16:69798481 | GTTTCAGGTTAGGGA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs200857360 | snp | A/G | 0.000217484 | 0.0104257 | missense | WWP2 | GRCh38.p7 | 16:69917882 | AAAGATTCCTCTACC[A/G]GGTGAGAGGGCAGGC | 11060 |
rs200875658 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69774968 | AGCAAGACTGTCTCA[A/G]AAAAAAAAAAAAAAG | 11060 |
rs200900386 | snp | A/G | 5.25569e-05 | 0.00512598 | intron-variant | WWP2 | GRCh38.p7 | 16:69842166 | TAAGAAGTTGCTTAG[A/G]GCTATTGAAAACATG | 11060 |
rs200912202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896411 | CAGGTGTGAACCACC[A/G]TGCCCATCCTTACTG | 11060 |
rs200950554 | snp | A/G/T | 3.30214e-05 | 0.00406323 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931498 | AAGTTCTTTTCTTTT[A/G/T]TTTTTTTCAGTCAAA | 11060 |
rs200955095 | in-del | -/TTTATTTATTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866271 | AAAAAGGTTTCACAT[-/TTTATTTATTTA]TTTATTTATTTATTT | 11060 |
rs200959851 | in-del | -/AAAACAAAAAAAAAAAAAAAAAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912919 | AGAACCAGTCTCTAC[-/AAAACAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAATA | 11060 |
rs200965935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902447 | AGTACTTTGAAGTAC[A/G]AAGACCTCGTGTAGT | 11060 |
rs200972549 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | WWP2 | GRCh38.p7 | 16:69809790 | AAAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 11060 |
rs200973575 | snp | A/G | 0.000659892 | 0.0181524 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931615 | AACCAGTGGCAGGCC[A/G]ACGCCCTCCTCCCAG | 11060 |
rs200978403 | snp | C/G/T | 3.30011e-05 | 0.00406195 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935957 | GGAGTCCATTGACCC[C/G/T]GAGTTCTACAACTCC | 11060 |
rs200998762 | in-del | -/TTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817660 | CTTTTTGTTAAACTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs201007253 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822016 | TAAGACCAGAAATGC[A/C]CACCACTATGCCCAG | 11060 |
rs201026114 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810305 | CTCTCTGAGGGGACA[-/T]TCGCCCTGGCCATGG | 11060 |
rs201042861 | in-del | -/AG | 0.0185938 | 0.0946107 | intron-variant | WWP2 | GRCh38.p7 | 16:69934442 | CCCTGTAGGTAGTGA[-/AG]AGTTTCCATGTTGCT | 11060 |
rs201053246 | snp | G/T | 0.00218608 | 0.0329888 | intron-variant | WWP2 | GRCh38.p7 | 16:69939447 | GTGGGAGGTCGGGGG[G/T]CCTCAGACCCGATGA | 11060 |
rs201076654 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861661 | TTTTTTTTTTTTTTT[A/G]TAATCCACATTTGAG | 11060 |
rs201082035 | snp | A/G | 0.000164954 | 0.00908018 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935933 | TAAGAGACCAACCCT[A/G]AAAGACCTGGAGTCC | 11060 |
rs201099315 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803375 | ATTTACATAAAAAAA[-/AC]ATTATCTTACACAAT | 11060 |
rs201105755 | snp | C/T | 0.00199809 | 0.0315445 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925469 | GATCCCCTGGGCCCC[C/T]TCCCTCCTGGCTGGG | 11060 |
rs201132574 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914101 | AAAAAAAAAAAAAAA[C/T]AAAGTGATAAATTTG | 11060 |
rs201135806 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777309 | TACTTTTATATTTTC[-/T]TTTTTTTTTGAAACG | 11060 |
rs201143088 | in-del | -/ACACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820826 | TGAATACATGCATAT[-/ACACAC]ACACACACACACACA | 11060 |
rs201149822 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781134 | TGGCTTTAAAAAAGG[-/A]AAAAAAAAAGAACTG | 11060 |
rs201160544 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840175 | GGAGAACAAAGGCAG[C/T]GTTGTCTCAGGCGGA | 11060 |
rs201183173 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875021 | AGTGAGACCTTGTGT[G/T]AAAAAAAAAAAAATT | 11060 |
rs201191026 | in-del | -/CAAAT | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69897929 | CAAAACAAAACAAAA[-/CAAAT]CAAAACAAAAAAAAC | 11060 |
rs201194810 | in-del | -/T | 0.0876345 | 0.190099 | intron-variant | WWP2 | GRCh38.p7 | 16:69790574 | AGCATCTTTTTTTTT[-/T]GTTTGTTTTTGAGAC | 11060 |
rs201202304 | in-del | -/TTTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800176 | AGCCTCCTCTGGTCT[-/TTTC]TTTTCGGCTGGGCAC | 11060 |
rs201204671 | snp | C/G | 0.00052953 | 0.016263 | intron-variant | WWP2 | GRCh38.p7 | 16:69917906 | GGCAGGCGCTTGGCC[C/G]GAGGTGGGGCCGCCT | 11060 |
rs201228009 | in-del | -/TTTC | 0.0941369 | 0.195465 | intron-variant | WWP2 | GRCh38.p7 | 16:69791224 | TACTTCTTTTCTTTT[-/TTTC]TTTCTTTCTTTTTTT | 11060 |
rs201266641 | snp | A/G/T | 1.69916e-05 | 0.00291471 | intron-variant | WWP2 | GRCh38.p7 | 16:69917681 | AGTGGGGTGGTCATT[A/G/T]TATTCATTCTGAGGT | 11060 |
rs201271252 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785227 | GGTGTGTGAGACTGT[C/G]TCAAAAAAAAAAAAA | 11060 |
rs201280028 | snp | C/G | 0.000197853 | 0.00994422 | intron-variant | WWP2 | GRCh38.p7 | 16:69925509 | GAGTTCTCTTCCTGG[C/G]CCTTGGCCTTCCGTC | 11060 |
rs201287506 | snp | C/T | 0.000381944 | 0.013814 | missense | WWP2 | GRCh38.p7 | 16:69842119 | TTTGGTGGAAGATCC[C/T]GGTAAGACCCCCCTT | 11060 |
rs201294551 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813162 | TTATTTCTGGTGTAA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs201303495 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912301 | CATCTCAAAAAAAAA[-/C]AAAACAAAACCTCAT | 11060 |
rs201359233 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914905 | CTTGGAAGCTACTCC[A/G]TGATTTATCGCACCA | 11060 |
rs201363823 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893876 | TGTTCATAAAGGATC[A/G]CTCTTCCTGCACTGG | 11060 |
rs201376399 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814458 | ACACTATTTATAAAT[A/T]TTTACAAATTCCTTC | 11060 |
rs201381531 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852012 | ACAAAACAAAACAAA[A/G]TTTTTAACTTGCTTG | 11060 |
rs201414304 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808668 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 11060 |
rs201449256 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69829096 | GAGCCGTCTTCGATA[-/C]CCGACCCCTCTTGCC | 11060 |
rs201464515 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798480 | GGTTTCAGGTTAGGG[A/T]TTTTTTTTTTTTTTT | 11060 |
rs201469783 | snp | A/G | 0.00199806 | 0.0315442 | missense | WWP2 | GRCh38.p7 | 16:69937582 | AGGAGATAGACATGA[A/G]CGACTGGCAGAAGAG | 11060 |
rs201483306 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806961 | ATTTATTTATTCATT[C/T]ATTCATTCATTCATT | 11060 |
rs201494557 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915876 | CCATGTCTACAAAAA[-/T]TTTTTTTAAAAAATT | 11060 |
rs201531336 | snp | A/G | 0.00087813 | 0.0209355 | intron-variant | WWP2 | GRCh38.p7 | 16:69929536 | GACCCAGGGGTAAGG[A/G]CTTGGGCTGAGAGGG | 11060 |
rs201541459 | in-del | -/T | 0.0444908 | 0.142359 | intron-variant | WWP2 | GRCh38.p7 | 16:69778262 | ATTTTGACTTTCCCA[-/T]CCCCCTCCCAATAAG | 11060 |
rs201555672 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873681 | AAAACTCAGTGGCTT[G/T]TGGAGGAGGGCAGTG | 11060 |
rs201569690 | snp | C/T | 0.000571294 | 0.0168914 | intron-variant | WWP2 | GRCh38.p7 | 16:69936491 | CCGCTCCAGGGGTGG[C/T]GTGGAGATCTAGTGG | 11060 |
rs201577619 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848462 | CTCAAAAAAAAAAAA[-/A]CAAACAAACAAGAAG | 11060 |
rs201592963 | in-del | -/AG | 0.0260105 | 0.111035 | intron-variant | WWP2 | GRCh38.p7 | 16:69802624 | TTTTTTTTTTGAGAC[-/AG]GGTCTCGCACTGTCG | 11060 |
rs201613294 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766263 | CTCGTCCACAAAGCC[-/T]ACTGGCTGTACTTCA | 11060 |
rs201620630 | snp | A/C | 0.000399281 | 0.0141238 | missense | WWP2 | GRCh38.p7 | 16:69934063 | CTGCCTGCAGATCAA[A/C]CCCGCCTCCTCCATC | 11060 |
rs201663365 | in-del | -/AAA | 0.384209 | 0.210922 | intron-variant | WWP2 | GRCh38.p7 | 16:69826724 | CTCTAATAAAAATAC[-/AAA]AAAAAAAAAAAAAAT | 11060 |
rs201675073 | snp | C/T | 0.000199435 | 0.00998387 | intron-variant | WWP2 | GRCh38.p7 | 16:69939441 | GTTTTAGTGGGAGGT[C/T]GGGGGGCCTCAGACC | 11060 |
rs201692116 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912920 | GAACCAGTCTCTACA[A/G]AACAAAAAAAAAAAA | 11060 |
rs201693624 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791232 | TTTCTTTTTTTCTTT[C/T]TTTTTTTTTTTTTGA | 11060 |
rs201701573 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908709 | TCCTTTCTAACAGGG[C/G]CCTATGCCTTTCCAC | 11060 |
rs201711599 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778173 | CTCATACTATAAATA[A/T]ATATATATATATATA | 11060 |
rs201713722 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878680 | TTTTATACATGGTTT[A/C]ATGTATCTATGTGCT | 11060 |
rs201720726 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69820825 | ATGAATACATGCATA[C/T]ACACACACACACACA | 11060 |
rs201729054 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923327 | TGGGGGGGTGGGGGG[-/GG]TGCGTTCTGATAGAA | 11060 |
rs201731313 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854408 | GGAACTGGATGGCTC[C/T]TTTTAAAGTGCCAAG | 11060 |
rs201733788 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767031 | GTACTGGAATAGGGG[-/T]TTTTGTTTTTTTTTT | 11060 |
rs201734636 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830237 | TGGGATTACAGGCGA[A/C]AACCACCATGCCCGG | 11060 |
rs201784061 | snp | A/C/T | 3.30421e-05 | 0.0040645 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908893 | ACTCTGGAACTGACA[A/C/T]CATGAGTCACCCAAT | 11060 |
rs201784369 | in-del | -/A | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69804215 | CTTTATGTTTTCAGC[-/A]TTTTCTTTCATGCTT | 11060 |
rs201804554 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821723 | TTTCTTTTCTTTCTT[A/T]CTTTTTTTTTTTTTT | 11060 |
rs201824922 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784094 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 11060 |
rs201831512 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809791 | AAGAGAGAGAGAGAC[A/G]GAGAGAGAGAGAGAG | 11060 |
rs201858298 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | WWP2 | GRCh38.p7 | 16:69840134 | CCCACAGTGGAGAAC[A/G]TGCAGCTGACCCTGA | 11060 |
rs201868868 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851982 | GCAGCGAGATTCCAG[A/C]TAAAACAAAACAAAA | 11060 |
rs201890122 | snp | C/G | 0.00016487 | 0.00907786 | missense | WWP2 | GRCh38.p7 | 16:69888190 | AGGAGAGGAACCCAG[C/G]ACTTCGGGTACACAG | 11060 |
rs201931986 | in-del | -/GTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893581 | TTGTTTTTGTTTTTG[-/GTT]TTTTTGTTTTTTTGA | 11060 |
rs201934863 | snp | A/G/T | 1.64898e-05 | 0.00287135 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925404 | TTTTTGTAACCTCTG[A/G/T]GTTCTGCTGTGTTTC | 11060 |
rs201938968 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935960 | GTCCATTGACCCTGA[A/G]TTCTACAACTCCATT | 11060 |
rs201942149 | snp | C/T | 5.08375e-05 | 0.00504145 | intron-variant | WWP2 | GRCh38.p7 | 16:69871757 | GAAACACTTCTGTCC[C/T]TTTCACAGTGACTTA | 11060 |
rs202010744 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831126 | ATCAGTCACATCTTC[A/G]TCGGGCTTCAGAGAC | 11060 |
rs202032113 | in-del | -/TTTTTTTTTTTT | 0.228547 | 0.249078 | intron-variant | WWP2 | GRCh38.p7 | 16:69817660 | CTTTTTGTTAAACTC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTA | 11060 |
rs202048729 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883402 | TCTAAGAATGTGCGC[A/G]CACACACACACACAC | 11060 |
rs202074799 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925120 | TCCTACCATGCCAGG[A/G]CTGCTCCCTGCCTCC | 11060 |
rs202095634 | snp | A/G/T | 0.000150292 | 0.00866762 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931886 | GACTATGGGGGCATC[A/G/T]CCAGGTGAGCTTGAG | 11060 |
rs202098180 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798482 | TTTCAGGTTAGGGAT[G/T]TTTTTTTTTTTTTTA | 11060 |
rs202107837 | in-del | -/C | 0.040671 | 0.13668 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924505 | AACTTTTTGACAACA[-/C]CCCCCTTCCCCGCAG | 11060 |
rs202118790 | snp | C/T | 0.000184442 | 0.00960139 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931486 | AGGCTCGATTTAAAG[C/T]TCTTTTCTTTTTTTT | 11060 |
rs202118904 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914434 | ATCCTTCTTCTCAGC[A/T]GTAGAGCAGGACCTT | 11060 |
rs202141630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917925 | GTGGGGCCGCCTCCC[C/T]GCGCTTGCGAATGTG | 11060 |
rs202145452 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805096 | CCAGGCTGGAGTACA[A/G]TGGCATGATCTTGGC | 11060 |
rs202157148 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778107 | CACACACACACACAC[-/AT]GTATATACATACACA | 11060 |
rs202162910 | in-del | -/CGATTCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794020 | CCTCCTGGGTTCAAG[-/CGATTCT]CGTGTCTTAGCCTCC | 11060 |
rs202164711 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822101 | CAAACTCGTGGGCTC[-/A]AGCGATCCTTCCACC | 11060 |
rs202191991 | in-del | -/T | 0.311614 | 0.242289 | intron-variant | WWP2 | GRCh38.p7 | 16:69852283 | TCTCTTTTTTTTTTT[-/T]GAGAAAGAGCCTCAC | 11060 |
rs202196997 | snp | A/G | 1.69599e-05 | 0.00291199 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939916 | GTATGCCATTGAGGA[A/G]ACCGAGGGCTTTGGA | 11060 |
rs202198115 | in-del | -/TTG | 0.0741063 | 0.177655 | intron-variant | WWP2 | GRCh38.p7 | 16:69893559 | AGAATGCTGTTTTTT[-/TTG]TTTGTTTGTTTTTGT | 11060 |
rs202199422 | in-del | -/GC/GCG | 0.0829062 | 0.185956 | intron-variant | WWP2 | GRCh38.p7 | 16:69883397 | ATGTTCTAAGAATGT[-/GC/GCG]GCGCACACACACACA | 11060 |
rs202205376 | snp | C/T | 0.000577667 | 0.0169853 | intron-variant | WWP2 | GRCh38.p7 | 16:69925530 | GCCTTCCGTCAGCCA[C/T]GGTGCTCTGTCCTCT | 11060 |
rs202206764 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917946 | TGCGAATGTGCAGCC[A/T]CGTGTTCTCTGTTGA | 11060 |
rs202227334 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69900965 | GAGTTATTAAAAGGT[-/A]TAGTGTGCTTAGATT | 11060 |
rs367545708 | snp | C/G | 1.6757e-05 | 0.00289452 | intron-variant | WWP2 | GRCh38.p7 | 16:69929571 | CGGGCTGGGCTGGGT[C/G]TCTGTGCAGCTCCAG | 11060 |
rs367556265 | snp | C/T | 0.000116049 | 0.00761649 | intron-variant | WWP2 | GRCh38.p7 | 16:69787112 | AATGTCTTCATCTTG[C/T]CTACGCCCAGGGAAG | 11060 |
rs367562242 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69933967 | CTGTCTCTTCCCTCA[C/T]AGAGAGTGGTTTTTC | 11060 |
rs367602537 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847655 | TCAGGTGATCTGCCC[A/G]CCTCGGCCTCCTAAA | 11060 |
rs367606740 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | WWP2 | GRCh38.p7 | 16:69803087 | TTGGATATTACTTGT[-/A]AAAAAAAAAAAGCCT | 11060 |
rs367661487 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905792 | AAATTTCAGTTCATC[G/T]TCCTTTTCTGCCCAT | 11060 |
rs367673055 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896758 | TAAACACTAACTACA[A/G]CTACCATGTATTCTA | 11060 |
rs367680144 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873439 | ACTTGAGTGAACTGA[C/G]TAGCCCACCCTGAGC | 11060 |
rs367707093 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857023 | TTCTCGTGATTCTTG[A/G]TATCTTTAGAGTTGT | 11060 |
rs367716000 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842943 | AAACTGTTGGGATTA[-/C]CAGCCATAAGCCACT | 11060 |
rs367725046 | in-del | -/TCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865406 | GATTGCTGAATTTTA[-/TCT]AGAGTTCTCTATCAA | 11060 |
rs367725310 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826661 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 11060 |
rs367733294 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842586 | CATATGGTATTTGGT[G/T]TTCTGTTTCTGCATT | 11060 |
rs367756515 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920830 | AAGCAATTTTTTTTT[-/T]CCCTTAAAAGCCCCA | 11060 |
rs367812375 | snp | A/C/G/T | 0.000100341 | 0.00708253 | intron-variant | WWP2 | GRCh38.p7 | 16:69936478 | GGCGCCGGGGGCTCC[A/C/G/T]CTCCAGGGGTGGCGT | 11060 |
rs367812535 | snp | A/G | 1.65203e-05 | 0.002874 | missense | WWP2 | GRCh38.p7 | 16:69917732 | AACGCACAGATCCCC[A/G]AGGCAGGTTTTACTA | 11060 |
rs367837270 | snp | C/T | 4.94817e-05 | 0.00497377 | missense | WWP2 | GRCh38.p7 | 16:69798786 | AAGAAGACTGGGAAG[C/T]GCATTGGGAGCTCTG | 11060 |
rs367852855 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818000 | GTGTTTCAAGTTTTT[G/T]ATGCCTGCTGCCTGT | 11060 |
rs367886588 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877864 | CCACGCTGGAGTGCA[A/G]TGGCATGATCTTGGC | 11060 |
rs367888949 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861556 | GGTGTGGAATGGAGC[C/T]GTAAATTGCGCTTGC | 11060 |
rs367896673 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69894453 | GTCTGCACGTTTTAA[A/G/T]AACTGAAGGCTGCTG | 11060 |
rs367921536 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826601 | AAAAAAAAGTGGAGC[C/T]GGGCACGGTGGCTAA | 11060 |
rs367923842 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883939 | GCTTTTGTTCTTTTC[C/G]TGGTCAGCTATTTCG | 11060 |
rs367937061 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918845 | TTTTTCCTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 11060 |
rs367939643 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781860 | AGAGCTAGAGAGAAA[C/T]GTGAGGGGCTGAACT | 11060 |
rs367941145 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851844 | AAAAATTAGCTGGGC[A/G]TGGTAGTGCGCTCCT | 11060 |
rs367950075 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899713 | GCCTGGGTGACAGAG[A/T]GAGACTCCGTCTCAA | 11060 |
rs367952800 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868204 | GGGTGGTGGCTGGCC[A/C]CGGGCAGGGAGGTGG | 11060 |
rs367967522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813248 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 11060 |
rs367985081 | snp | A/G | 0.000437904 | 0.0147905 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940904 | GCCTTGCCGCCTTCA[A/G]TAGAGAAGAAATCCC | 11060 |
rs367985538 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904989 | AACCCAAATTAGGAG[C/T]ATATGTTTTTTGTAA | 11060 |
rs367986754 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931746 | CCCTGTCCCTCCCGC[C/T]CCTGCCTGCTGTGGA | 11060 |
rs367989999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774594 | AATGTTTTGCAGATA[C/T]TCTCAGTTTCTTCCT | 11060 |
rs368037078 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920339 | TGCACACTTTCTTGG[G/T]CTAGGCTTCCCACCC | 11060 |
rs368037172 | snp | A/G | 8.34328e-05 | 0.00645828 | intron-variant | WWP2 | GRCh38.p7 | 16:69929557 | GCTGAGAGGGGGGCC[A/G]GGCTGGGCTGGGTCT | 11060 |
rs368056509 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69798956 | CTATGGTACCCAAGG[-/T]GACTCTTTTTAGGTG | 11060 |
rs368058591 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69905075 | ATAAGGCAGACGCCC[-/A]GCTGTAGCTGTTTAG | 11060 |
rs368093004 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899931 | AACTTGCCTTTTCTA[C/T]CCAATATATTGTAAA | 11060 |
rs368093769 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896895 | AACTTAAGCAATTTG[C/G]CTGGCACCACATATA | 11060 |
rs368107386 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908010 | CTTTGGCAGGCCAAG[A/G]TGGGTGGGTCGCTTG | 11060 |
rs368110457 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69934974 | CTGTCAGAAAGTGAG[C/G]CAGTTCTGGGGAGGG | 11060 |
rs368110705 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915854 | GCCTGAGCCACACGG[A/G]GAGGCTTCCATGTCT | 11060 |
rs368137916 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904964 | CTAACTTAGTACGTA[A/C]ACCAACCAAAACCCA | 11060 |
rs368155570 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849924 | TTGCATAGATATTTA[C/T]TTGGCATTTACTCTG | 11060 |
rs368159832 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794714 | CTGCATTCTTTAAAA[C/T]AGCTGGTGGAAGTCT | 11060 |
rs368161973 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855476 | ATAATGCAGAATCCC[A/G]GAGTGTTCCTTTTTT | 11060 |
rs368166399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872377 | GCCCACTGCCACGCC[C/T]GGCTAATTTTTTGTG | 11060 |
rs368182407 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69929422 | GTGTTTGAATCTGAT[A/G]TTCTTTCTTTCTTCT | 11060 |
rs368186747 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917793 | GCAGCGTCCGACCGC[A/G]GAGTACGTGCGCAAC | 11060 |
rs368187158 | snp | C/G | 4.89512e-05 | 0.00494704 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933086 | GCGCCCTGTGTGTGT[C/G]TCTCTCTGTGTCCTG | 11060 |
rs368189035 | snp | A/G | 4.52427e-05 | 0.00475598 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939960 | GGCCGCCCCTCCCAC[A/G]CCCCCCAGCGCACAT | 11060 |
rs368202582 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776779 | GTTGTGGTGAGCCGA[C/G]ATTGTGCCATTGCAC | 11060 |
rs368203015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69851595 | CCTCCTCCACAGTTT[A/G]TTCATTCATTTACTG | 11060 |
rs368204964 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817949 | TTTCCCTACAGTAAA[G/T]TCCCAGGCATGCAGT | 11060 |
rs368206619 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | WWP2 | GRCh38.p7 | 16:69819495 | CACTGGCCTTAAATC[G/T]CTCCTGAAACTGACC | 11060 |
rs368232669 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940875 | AGGGGTTGAGGTCCC[A/G]AGCGCCACTCCTAGC | 11060 |
rs368250248 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908337 | GATCTTGTGGAGGGG[-/G]TCTATGAAACCCAGA | 11060 |
rs368270351 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823917 | GTTGGGCCATCTTCT[C/G]CAAGGGCCTGTGCTG | 11060 |
rs368283112 | snp | A/G | 8.33952e-05 | 0.00645683 | intron-variant | WWP2 | GRCh38.p7 | 16:69930297 | GCAGTGTCAGGAGCC[A/G]AGGCCCAGGCTGTCC | 11060 |
rs368287382 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896518 | GCTTCCAAAGAGAGG[A/G]AGTGATGTGTTACAT | 11060 |
rs368303803 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854362 | TGTGGTTTGGTGAGA[A/T]GAGGTTCGACTTTTC | 11060 |
rs368324411 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884272 | TAACTTGAAGAGCTT[C/T]GTTCACCTCCCCTTT | 11060 |
rs368329156 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900625 | CCTCCTGGACTCAAG[C/T]GATTCTCCTGCCTCA | 11060 |
rs368331143 | in-del | -/T | 0.0228237 | 0.10436 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931494 | TTTAAAGTTCTTTTC[-/T]TTTTTTTTTTTCAGT | 11060 |
rs368343023 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835269 | TGCTATTTATAACTA[A/G]GGTTCTAGTATATGT | 11060 |
rs368352017 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870020 | CTTGAGTTCAGGCTT[C/T]CTGTCCCATCTTCTG | 11060 |
rs368360405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826363 | ACAAGGCCAGGAGTA[C/T]GAGACCAGCTTGGCC | 11060 |
rs368368822 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69786987 | TTCTTTTTTCTGTTT[A/G]TCTTACAGCTTCACG | 11060 |
rs368384774 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823800 | CATCACCTTGTCTTC[A/C]GAAGAAACTTTTCTG | 11060 |
rs368459644 | snp | C/T | 3.07972e-05 | 0.00392398 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939083 | GCAGTTTGTCACCGG[C/T]ACCTGCCGCCTGCCC | 11060 |
rs368466074 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777140 | ATATGGATATATATA[C/T]ACATATGTGTATATA | 11060 |
rs368468132 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807908 | AGGCTGCAGTAAGCT[A/G]TAATCATGCTGCACT | 11060 |
rs368474183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876452 | TCACTATAACCTACA[A/C]CTCCCGGGTTCAAGT | 11060 |
rs368479151 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914004 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAAC | 11060 |
rs368497082 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771467 | GGCCAGGCTGGTCTC[A/G]AAATCCTGACCTCAA | 11060 |
rs368500964 | snp | C/T | 9.88533e-05 | 0.00702971 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931129 | AAATCGCATGAACCC[C/T]TGAACATCTTTGCTC | 11060 |
rs368543461 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935565 | GGAGCCAGCCGGCCA[C/G]CGTGCGGGGCAGATG | 11060 |
rs368547603 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820825 | TGAATACATGCATAT[-/AC]ACACACACACACACA | 11060 |
rs368599518 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778190 | TATATATATATATAT[-/A]TATTTTTTTTTTTTT | 11060 |
rs368601937 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762063 | CAGTCTGAAGGTCTC[A/G]TTTCACCTGTAAAAT | 11060 |
rs368619192 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861208 | AGGGTACCTCAAGCC[A/G]TCAATGGCCACGTTG | 11060 |
rs368622979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876747 | TGGATGTTGTGTTAG[C/T]GGGCATGAAAACAAC | 11060 |
rs368666194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69864289 | GGGAGGATTGCAGGA[A/G]CCCAGGAGGCTGCAG | 11060 |
rs368668201 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69779796 | TTAGTGCTTTAACCC[-/CT]GTTAACTAAAAGCCC | 11060 |
rs368669172 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832352 | ATTTTATGAAAATCC[A/C]GACATACTTCAACTA | 11060 |
rs368680621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69794157 | TCCTGGTCTCAAGTG[A/G]TCTACCTCCCTTAGC | 11060 |
rs368682068 | snp | G/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909546 | CCATGGATGGGCTGC[G/T]TTTAGCTCCAGTTTT | 11060 |
rs368711553 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938435 | CCAGCCTGGCCAAAA[C/T]AGTGAAACCCTCTTT | 11060 |
rs368726483 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69891284 | GTTATTAATTTACCC[A/C]TGGTGTTCCAGAGTC | 11060 |
rs368747971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69881962 | CCTCCCAAAGTGCTG[A/G]GATTATAGGGGTGAG | 11060 |
rs368750070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69856730 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 11060 |
rs368754865 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885026 | ACATTGTTTTAATTG[C/T]TGTAGCTTTGTAGTA | 11060 |
rs368788146 | snp | C/T | 0.000190247 | 0.00975128 | intron-variant | WWP2 | GRCh38.p7 | 16:69929398 | TCAGGGAAAGGACAC[C/T]GGCTCTCCGTGTTTG | 11060 |
rs368793565 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905123 | CTTCCGTGTTCAGCC[C/T]CTAAAGACTTGCCGC | 11060 |
rs368799652 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791236 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTGAGACG | 11060 |
rs368825667 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834179 | CCTTGTCCCAAGGCC[C/T]GACTGGGAGGCTCTG | 11060 |
rs368834203 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797017 | CAGGCTAGGATAGAC[G/T]TGCCATTACAGGCAA | 11060 |
rs368855527 | snp | C/T | 8.25144e-05 | 0.00642265 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925381 | TGATTGATTTTTTCA[C/T]CAGTGGCTTTTTGTA | 11060 |
rs368881090 | snp | A/G | 0.000117124 | 0.0076517 | intron-variant | WWP2 | GRCh38.p7 | 16:69936016 | CCCTTGCCCCACCGC[A/G]CTGATAGGAGGGACG | 11060 |
rs368916598 | in-del | -/TTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812146 | TTGGCATCGGCGTTG[-/TTG]AAGAGTACAGACCTT | 11060 |
rs368952818 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916187 | GGGAGTCAATGGAAG[-/TGT]TGTTGTTGTTGTTGT | 11060 |
rs368989395 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832206 | ACAAAAACTGTTATA[A/G]GAAATGTGAAACATA | 11060 |
rs369017046 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69935169 | TGTTTCAATTCTCCT[A/T]TCCTTCGCTTCTTCC | 11060 |
rs369075876 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816753 | TATACATATACACAC[A/G]TATACATATACACAT | 11060 |
rs369088259 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853522 | AATCACACCCAGAGC[C/G]TATCTGCAGGAGGGT | 11060 |
rs369091251 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895473 | CAATGTCAGATCGGT[A/G]CAAAAGTTCCTAAAG | 11060 |
rs369093279 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773447 | GCCTCCCAAAGTGCT[A/G]GAATTACAGGCATGA | 11060 |
rs369099762 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911511 | TATGCTGGAGTGGAA[A/G]GGTTGTATGAAGTAA | 11060 |
rs369102218 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793412 | TTGCATTAGAGAAAG[A/G]GTTTAATTGACACAA | 11060 |
rs369106756 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906771 | TGTTTTCCTAGCTAC[A/T]TGGGAGGCTGAGGCA | 11060 |
rs369118169 | snp | C/T | 0.000181433 | 0.00952279 | intron-variant | WWP2 | GRCh38.p7 | 16:69908731 | CCTTTCCACTGTGTG[C/T]CTCATGCTACCCTTG | 11060 |
rs369140666 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879381 | CAATAACATTTCCCC[C/G]CAACCTGACCGGCCC | 11060 |
rs369162893 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847369 | GGATTACAGGCATGA[A/G]CCACCATGCCCTGCC | 11060 |
rs369166433 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940745 | CTTTGGGTCCAAGAG[C/T]TTCCCAAACAGCCAC | 11060 |
rs369173447 | in-del | -/CACACACACACACACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912392 | ACACACACACACACA[-/CACACACACACACACACACA]GCCTCATGACTGCCT | 11060 |
rs369186621 | snp | A/G | 1.672e-05 | 0.00289132 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931767 | CTGCTGTGGAAGGGA[A/G]AGTGGCAGGCTGGCC | 11060 |
rs369223567 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921935 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCACCT | 11060 |
rs369233171 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | WWP2 | GRCh38.p7 | 16:69929748 | CTGGTGGATGGAGGG[C/T]GGCCCGGCTGGCGGG | 11060 |
rs369250998 | in-del | -/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837248 | TAATTAATTTTTTTT[-/T]AGTGACAGAGTCTCA | 11060 |
rs369263991 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906300 | GATGATCTTGATCTC[C/G]TGACCTTGTGATCTG | 11060 |
rs369279393 | snp | G/T | 1.64822e-05 | 0.00287068 | missense | WWP2 | GRCh38.p7 | 16:69930180 | AGATGAAATACACCA[G/T]CGAGGGGGTGCGATA | 11060 |
rs369279958 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799051 | AGGGGAAAGGATATA[-/A]TGTGGGTGTCTGCCT | 11060 |
rs369288365 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832852 | CTGGCCCAACCTTTT[A/T]ATTTTTTATTTTTAT | 11060 |
rs369288782 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811763 | AGTCTCAAAAAAATA[A/C]AAGATTCAAATTCAG | 11060 |
rs369297474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917569 | CAGAGGCAACCACAG[A/G]TGTCTGCTATAATCA | 11060 |
rs369343925 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863002 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCGCCA | 11060 |
rs369344773 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789315 | ACTCACTGTAACCTC[C/T]GCCTCCCGGGTTCAA | 11060 |
rs369355565 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882144 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 11060 |
rs369381187 | snp | A/G | 3.2987e-05 | 0.00406108 | missense | WWP2 | GRCh38.p7 | 16:69799250 | GAACTGCTAGGCACC[A/G]CATCTGTCAACCTCT | 11060 |
rs369385873 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906059 | TATCTGTTTCTTTTT[A/C]TTTCCTTTTCTTTTC | 11060 |
rs369387924 | snp | G/T | 1.65833e-05 | 0.00287948 | intron-variant | WWP2 | GRCh38.p7 | 16:69939438 | CTGGTTTTAGTGGGA[G/T]GTCGGGGGGCCTCAG | 11060 |
rs369389628 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800173 | TGAGCCTCCTCTGGT[-/T]CTTTTCTTTTCGGCT | 11060 |
rs369395233 | snp | C/T | 0.000507743 | 0.0159253 | intron-variant | WWP2 | GRCh38.p7 | 16:69939164 | TCCTGGCTGGCAGTG[C/T]GGACAGCTCAGAGGG | 11060 |
rs369404669 | in-del | -/AC | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910010 | TTTGGCTGTTTTTGT[-/AC]TTCATTGGCAGAGTT | 11060 |
rs369405724 | snp | A/C/G/T | 0.000169608 | 0.00920765 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931464 | CAGGAGAACAGATGA[A/C/G/T]CACTTGAGGCTCGAT | 11060 |
rs369417518 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844364 | TAGAGAGGAAGGAAT[A/T]CTTGAGTATTTCACT | 11060 |
rs369440388 | snp | C/T | 1.65935e-05 | 0.00288036 | intron-variant | WWP2 | GRCh38.p7 | 16:69798671 | TGACTTTTTCTTTCT[C/T]TCTCTCCCAGTGGTG | 11060 |
rs369476110 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920692 | TGGAAGACTGGCGGG[G/T]GGGAGGATCACTTGA | 11060 |
rs369500025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844045 | GTGACTGGCAAGTGG[C/T]GGGAGCAAGACAAGA | 11060 |
rs369500889 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940901 | CTAGCCTTGCCGCCT[C/T]CAATAGAGAAGAAAT | 11060 |
rs369518584 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69936802 | GTCTCACGTGTGCCC[A/G]TTCTCCGTGCCTGTT | 11060 |
rs369521463 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903083 | GCAACTATTCTTCTC[A/G]CTAAGCCAGTTGAGG | 11060 |
rs369526960 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897995 | GCATGCCTTTTTGTG[C/T]ATGTGGTTTTTTCTT | 11060 |
rs369536999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803998 | AGGCTACTGAAGGAT[C/T]AAAAAAAAGTGTTTA | 11060 |
rs369558285 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864030 | ATGAGCTTTTGCATA[C/T]AGGCTTTTATGCAAA | 11060 |
rs369569721 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798481 | TTTCAGGTTAGGGAT[-/G]TTTTTTTTTTTTTTT | 11060 |
rs369570022 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841596 | TATTGAAGGGTTTCT[C/T]GCAGAAGACTATGAT | 11060 |
rs369576893 | snp | C/T | 8.35247e-05 | 0.00646184 | intron-variant | WWP2 | GRCh38.p7 | 16:69936013 | GCCCCCTTGCCCCAC[C/T]GCGCTGATAGGAGGG | 11060 |
rs369584924 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862121 | CCCCGGCTGGAGTGC[A/G]ATGGTGTGATCTCGG | 11060 |
rs369585040 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793657 | GGGCCCAGGCAAAGT[C/T]AGTAGATTGCCAGAA | 11060 |
rs369653281 | snp | A/T | 6.59359e-05 | 0.00574139 | missense | WWP2 | GRCh38.p7 | 16:69888043 | TGCATCTTCAGTGAA[A/T]GATGAACCCACAACA | 11060 |
rs369670303 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792138 | TGTGACTGCGCGGTT[A/T]CCAGTTCCCTTGTGC | 11060 |
rs369703090 | in-del | -/CTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885150 | ACACACATTCTTCTT[-/CTT]TAGAATGTTCATGGC | 11060 |
rs369705784 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881891 | AGAGACAGAGTTTTG[C/T]CATGTTGGCCAGGCT | 11060 |
rs369713650 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897398 | GTGAGTCACTGTGCC[A/C]GGCACCTGAGGAGGT | 11060 |
rs369726866 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798291 | TGCAAGCAGTCTATT[C/T]GACAATGAAAGAATA | 11060 |
rs369735456 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866868 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 11060 |
rs369759234 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817379 | TTAGCCTCCCGAATA[A/G]TTGGGATTACAGATG | 11060 |
rs369761441 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810267 | ACGTCCCGCAGTGGC[A/G]GATGGTCAACCTGGG | 11060 |
rs369773162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69878184 | TATCAAAGATCACTG[A/G]TCACAGATCTCCATG | 11060 |
rs369781188 | snp | C/T | 6.67468e-05 | 0.00577658 | intron-variant | WWP2 | GRCh38.p7 | 16:69799299 | ATGGGGGCAAAAGTA[C/T]GTATGATGAAGGGGG | 11060 |
rs369794570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774238 | TCCTTCCTTGTATTC[C/T]CCAGACATGCTGTCA | 11060 |
rs369812987 | snp | A/G/T | 3.56958e-05 | 0.00422453 | missense | WWP2 | GRCh38.p7 | 16:69871914 | ACTCAGGCCACAGTG[A/G/T]CTTGGCCAATGGCAC | 11060 |
rs369827464 | snp | A/G | 0.0001179 | 0.00767698 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871807 | TTGAACCCCCAGGAC[A/G]CACAGACATTCGGGT | 11060 |
rs369830448 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767113 | GGCTACTCTTCCAAC[G/T]GTGCATCTTTATAGC | 11060 |
rs369841334 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | WWP2 | GRCh38.p7 | 16:69935235 | TAGGAGGACCCAAGC[A/G]CCCCATGAGCCTGTG | 11060 |
rs369888251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69911264 | CAATAAGTATTGGAC[C/T]TAGTAGCTCAGGGTG | 11060 |
rs369893626 | snp | A/C/G | 4.95432e-05 | 0.0049769 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917826 | TGAGCAGTGGCAGTC[A/C/G]CAGCGGAATCAGCTC | 11060 |
rs369934507 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889147 | AGTGATATCCTGCCT[-/AC]ACACACACACACACA | 11060 |
rs369943943 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892316 | CATCTACATTAGGTA[C/T]TTCTCCTAATGCTAT | 11060 |
rs369952941 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805143 | CTCCTGGGTTCAAGC[A/G]ATTCTCGTGCCTCAG | 11060 |
rs369976160 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819462 | GCCCGGTGCTGCTCT[A/C]CTGCCACTGACCCTT | 11060 |
rs369977148 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898027 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs369997102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782662 | GTAAAATGCTTATTA[C/T]AGACTAGTCTAGAAA | 11060 |
rs370013981 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772315 | ACTCTAATCATTCCC[A/G]AGATAGGCTTTTGCC | 11060 |
rs370025405 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901515 | CCTCCCGGGTTCATG[C/T]CATTCTCCTGCTTCA | 11060 |
rs370032967 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69774966 | AGAGCAAGACTGTCT[A/C]AAAAAAAAAAAAAAA | 11060 |
rs370046215 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844928 | CAAAGGCTGTCTCTT[C/T]GCCTCCTTAAAAGCC | 11060 |
rs370121521 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859460 | CTCAGGAGGCTGAGG[C/T]GGGAGGATCGCTTGA | 11060 |
rs370130499 | snp | G/T | 0.00025636 | 0.0113188 | intron-variant | WWP2 | GRCh38.p7 | 16:69799134 | CTAAGTTATAGGAAT[G/T]ATCTGCTTGGATGTA | 11060 |
rs370132804 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779163 | ACCATGTTGGCCAGG[C/G]TGGTCTCAAACTTCT | 11060 |
rs370138437 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821838 | GCTGGGATTATAGGC[A/G]TGAGCCACCATGCCC | 11060 |
rs370208026 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762409 | AGCGAGCGCTGGCGC[G/T]GGGGGCGCGGTGGGC | 11060 |
rs370282926 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890273 | TTTTCCTAGCATGCG[C/T]CACGCTACCTAACTC | 11060 |
rs370303463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69854936 | TCAAGGCCCACTGCA[A/G]CCTCAACCTCCAAGG | 11060 |
rs370347040 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904503 | TCTCCTGAGTAGGTA[C/T]GATTACAGGTATGTG | 11060 |
rs370392324 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846572 | CTAAAAATATAAAAA[C/T]TAGCTTGGCATGGTG | 11060 |
rs370400360 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761267 | CAACCTATCCAGACC[C/T]ATCTCTTAAAAAAAA | 11060 |
rs370402724 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806536 | ACCAACTGGGTCTGG[C/T]ATCTTGCTTTGAAAT | 11060 |
rs370439721 | in-del | -/CTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800179 | CTCCTCTGGTCTTTT[-/CTT]TTCGGCTGGGCACAT | 11060 |
rs370457139 | snp | G/T | 1.65127e-05 | 0.00287334 | missense | WWP2 | GRCh38.p7 | 16:69930253 | TCGCCCGGGGTTTGA[G/T]TCGGGGTAAGGACTT | 11060 |
rs370483971 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876277 | GGGTTTTGGCCACAT[C/G]CATCAGAGGAATCAT | 11060 |
rs370493874 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893078 | CCGGACTTAGGATCC[C/T]CCCCCATGCTGGTCA | 11060 |
rs370502505 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836046 | GGGCTCAGGTGATCC[A/T]CCCACCTCGGCCTCC | 11060 |
rs370526456 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820431 | GTATTTTTAGTAGAG[A/T]TGGGATTTCACCATG | 11060 |
rs370534607 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923724 | TTTCTATAGTCCTTC[A/C]CTTTTGCAAGGTCAC | 11060 |
rs370572580 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859934 | GACGACATACTTGAC[A/G]ACATACTCAAGGGTG | 11060 |
rs370572731 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69910996 | GCTCTCATTTCTGCT[C/G]TGTAATCACAGGGGA | 11060 |
rs370578049 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786151 | TCTTTTTTTTTTTTT[C/T]CTTCTTTTTTTGAGA | 11060 |
rs370579187 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778193 | TATATATATATATAT[-/A]TTTTTTTTTTTTGAG | 11060 |
rs370622871 | in-del | -/ACAGTAGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934925 | GCTGCCTCCTGGTGA[-/ACAGTAGA]CTGGCTGGTGCAGGG | 11060 |
rs370624389 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941506 | TCCCTGTGGCACGTT[A/G]CCATGGAAGCCGCTC | 11060 |
rs370632943 | snp | C/T | 1.65466e-05 | 0.00287628 | missense | WWP2 | GRCh38.p7 | 16:69937608 | AAGAGCACCATCTAC[C/T]GGCACTACACCAAGA | 11060 |
rs370645579 | snp | A/G/T | 0.000182829 | 0.00955952 | intron-variant | WWP2 | GRCh38.p7 | 16:69917934 | CCTCCCTGCGCTTGC[A/G/T]AATGTGCAGCCACGT | 11060 |
rs370654006 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69904689 | GTGTGCATTTTCATC[C/T]GGCCACTTTTGCCAG | 11060 |
rs370658283 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889002 | GGAGCCACCACACCC[A/G]GCCCTCTTGCCATCC | 11060 |
rs370718881 | snp | G/T | 8.82652e-05 | 0.00664265 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933125 | TTTACCCTATGGTAG[G/T]TTACGTCATGCTGTT | 11060 |
rs370746678 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863500 | AAAAATTAGCTGGGC[A/G]AGGTGGCAGGCGCCT | 11060 |
rs370746900 | snp | C/T | 2.84176e-05 | 0.00376935 | intron-variant | WWP2 | GRCh38.p7 | 16:69871976 | ACTGAAGCTGTGGGC[C/T]CTCACCCGTTCTAAC | 11060 |
rs370746957 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928924 | TGGAGGGTACAGGGG[C/T]GCAGGGTGCAGAGCA | 11060 |
rs370752159 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839957 | CAGTGATTTCATTAG[A/G]CATATTCCTTCCCAC | 11060 |
rs370778284 | snp | C/T | 0.000101549 | 0.00712489 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931907 | TGAGCTTGAGTGCCC[C/T]GGAAGGCTGCCCTGT | 11060 |
rs370808516 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806073 | AGGTGTGATGGTGTA[C/T]GCCTGTAGTCCCACC | 11060 |
rs370843807 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837506 | TCCCTGAGATGAGAC[C/T]ATGGAGAGGAAAATT | 11060 |
rs370860797 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69908821 | CCACAATACCAAGAC[C/G]ACCACCTGGGAGCGG | 11060 |
rs370864311 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799848 | CCAACGTGCCTCTAC[A/G]TCACGGACATATAAA | 11060 |
rs370872703 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765137 | GGGAGGTGGAGGCTG[C/T]AGTGAGTTGTGATCG | 11060 |
rs370924615 | snp | A/G | 0.000150066 | 0.00866087 | intron-variant | WWP2 | GRCh38.p7 | 16:69929559 | TGAGAGGGGGGCCGG[A/G]CTGGGCTGGGTCTCT | 11060 |
rs370941924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69876643 | TGCTGAGATTATAGG[C/T]GTGAGCCACTGTGCC | 11060 |
rs370944124 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828528 | TGCACCACCACACCC[C/T]GCTAATTTTGTATTT | 11060 |
rs370954783 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908523 | AATTTAGAGTGATCT[A/G]TAGTGGATCCTGGTC | 11060 |
rs370956872 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794181 | CCTTAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 11060 |
rs370960467 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761554 | CTCCAGCCTGGGCGA[C/T]AGAGCGAGGCTCCAT | 11060 |
rs370964763 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844762 | TAGTGTAAGCCTTAT[C/T]GGAGTCCTCTGCAGT | 11060 |
rs370966343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862226 | ATTCGCCACCATGCC[C/T]GGCTAATTTTGTATT | 11060 |
rs370970904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69812457 | GGCATGAGACACCGC[A/G]CCTGCCCCCAACCCC | 11060 |
rs370974522 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784857 | GCCTTTTCTTGAAAA[C/T]GAATGAAGTGAGCCC | 11060 |
rs370981847 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854347 | ATGGTGTTTGTGGCT[-/G]GTGGTTTGGTGAGAT | 11060 |
rs371003597 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769111 | ATCATGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 11060 |
rs371004702 | snp | A/G | 2.40168e-05 | 0.00346523 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939970 | CCCACGCCCCCCAGC[A/G]CACATGTAGTCCTGA | 11060 |
rs371043086 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809790 | AAGAGAGAGAGAGAC[-/AG]AGAGAGAGAGAGAGA | 11060 |
rs371055630 | snp | C/T | 1.71331e-05 | 0.00292682 | intron-variant | WWP2 | GRCh38.p7 | 16:69929406 | AGGACACCGGCTCTC[C/T]GTGTTTGAATCTGAT | 11060 |
rs371077322 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940285 | ATCCCCAGGGGCTGC[C/T]GCAGAGGCCGGAGAC | 11060 |
rs371086040 | snp | A/G | 3.31895e-05 | 0.00407353 | intron-variant | WWP2 | GRCh38.p7 | 16:69937503 | GCGAGTGGACGATGC[A/G]CGGGGAGGGACCTGC | 11060 |
rs371090870 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925180 | CGCCTCCTCCCCGTC[A/G]CTCTGCCTTTTCCAA | 11060 |
rs371100646 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794285 | ATCCCAGTACTTTAG[G/T]AGGCTGAGGCGGGTG | 11060 |
rs371111889 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879520 | TAATGTGGCATTTTT[C/G/T]ATTCATCCATGTTGT | 11060 |
rs371126312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882580 | GTCACAGGGGCTGTG[C/T]GACTGTGTAGCTGAG | 11060 |
rs371131486 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911784 | AAAAGTATTAAAAAG[C/G]CATAAACCTTCAACA | 11060 |
rs371137721 | snp | C/G | 2.16242e-05 | 0.0032881 | intron-variant | WWP2 | GRCh38.p7 | 16:69939822 | AGGGCTGACTGTCGT[C/G]CTTCCCCACTCTCAA | 11060 |
rs371170746 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885398 | TAGTCATTTATTAAA[C/T]AACTAATTTAGCCTG | 11060 |
rs371185823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69818388 | AATTTTTTATTTTTA[A/G]TAGAGATGGGGTTTC | 11060 |
rs371214769 | snp | C/T | 4.94442e-05 | 0.00497188 | missense | WWP2 | GRCh38.p7 | 16:69936383 | TACTGGGCAAGGTGA[C/T]GACCCACGAGCTGAA | 11060 |
rs371247908 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805680 | CAGTGGCATGATTAC[C/T]ACTCACTGTGGCCTC | 11060 |
rs371255105 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825912 | TACAGACGTGAGCCA[A/C]CACACCCTGCCTGGA | 11060 |
rs371273312 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912084 | CATGAAGTCAGGAGA[C/T]TGAGACCATCCTGGC | 11060 |
rs371336801 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849129 | GCCTATCCCAGAAAG[C/G]AAAGAAAAATAAACT | 11060 |
rs371352844 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930609 | GAGGCTGAGGTGGGA[A/G]GATCCCTTGAGCTCA | 11060 |
rs371353162 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893502 | TGCTGTCATTCACTG[C/G]CTTGACTGGCTTTGG | 11060 |
rs371366510 | in-del | -/AAAAAG | 0.0325976 | 0.123435 | intron-variant | WWP2 | GRCh38.p7 | 16:69765204 | AGACCCTGTCTCAAA[-/AAAAAG]AAAAAGAAAAAGAAA | 11060 |
rs371382535 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809542 | GAGGCCAAGGTGGGT[A/G]TATCACCTGAGGTCA | 11060 |
rs371401805 | snp | A/G | 5.00096e-05 | 0.00500023 | intron-variant | WWP2 | GRCh38.p7 | 16:69840296 | CCTCAGGACTGTGCC[A/G]GGACAGGGTGGGGCT | 11060 |
rs371454354 | snp | A/G | 4.94222e-05 | 0.00497078 | missense | WWP2 | GRCh38.p7 | 16:69840200 | GGCGGAGAGCTGACA[A/G]TTTTCCTGGACGGGC | 11060 |
rs371506598 | snp | C/T | 0.00443209 | 0.0468658 | intron-variant | WWP2 | GRCh38.p7 | 16:69939150 | CTCGCCCTCTGGCGT[C/T]CTGGCTGGCAGTGCG | 11060 |
rs371519415 | snp | C/G | 3.35464e-05 | 0.00409537 | intron-variant | WWP2 | GRCh38.p7 | 16:69936487 | GGCTCCGCTCCAGGG[C/G]TGGCGTGGAGATCTA | 11060 |
rs371532664 | snp | C/G/T | 6.5958e-05 | 0.00574241 | missense | WWP2 | GRCh38.p7 | 16:69917782 | ACCACCACCTGGCAG[C/G/T]GTCCGACCGCGGAGT | 11060 |
rs371554868 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880512 | GTAAGTAGGAACTGT[A/G]TTCATCTGTATATAC | 11060 |
rs371557834 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808682 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 11060 |
rs371565686 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69826235 | TCACACCACTGCACT[C/G]CAGCCTGGGTGACAA | 11060 |
rs371567707 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772412 | CACGTGAGCCCCAAA[A/G]CTGGGGGTTAGTCTG | 11060 |
rs371568523 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808343 | GATCCTCCCACTTTG[G/T]TCTCCAAAAATGCTG | 11060 |
rs371572210 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872133 | GTACAGCCAAGGTTA[C/T]TCTCCATATGACTGC | 11060 |
rs371577806 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762270 | GGTGGCCCGCACCTG[C/G]GAGCCTGGCCAGCCT | 11060 |
rs371588598 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838307 | CTTCACGGTGCACAG[C/T]TCTCAGGGACTAGAA | 11060 |
rs371612337 | snp | A/G | 6.60589e-05 | 0.00574675 | intron-variant | WWP2 | GRCh38.p7 | 16:69939314 | GACGTCTCTGCTGAC[A/G]TCGGCGTGTTTTACC | 11060 |
rs371625703 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931247 | GTTCTGGTACTGGGG[C/T]TCCCGTGGCAGTTGG | 11060 |
rs371626064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926710 | TTCAGCTTGGGGATC[C/T]CTTACGCAGATAGCT | 11060 |
rs371655513 | in-del | -/AACA | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69779940 | GTTAGAGATGAAGAT[-/AACA]AACAGTCATAAAAAC | 11060 |
rs371675192 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | WWP2 | GRCh38.p7 | 16:69869676 | TTCCTTACTCACAAG[C/T]ATACAAGCTCAATGA | 11060 |
rs371680787 | snp | A/G | 0.000132789 | 0.0081472 | intron-variant | WWP2 | GRCh38.p7 | 16:69787117 | CTTCATCTTGTCTAC[A/G]CCCAGGGAAGAGGGA | 11060 |
rs371686272 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790473 | GAAGGATTGGTTTTG[C/G]TATCTCTTGGGTGGC | 11060 |
rs371715040 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852679 | AATCTGGTTGTTCAT[A/G]TTCTTATTGTTGAGT | 11060 |
rs371719288 | snp | A/G | 0.000100773 | 0.00709761 | missense | WWP2 | GRCh38.p7 | 16:69871865 | GGCGAGCAAAGCCCC[A/G]GTGCTCGGAGCCGGC | 11060 |
rs371730052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69861797 | TTTTTTCATGCTTCT[A/G]TTTTAAGTGCCTGTT | 11060 |
rs371752584 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897289 | TATATTTTTTGTAGA[G/T]ATGGGGTTTTGCCGT | 11060 |
rs371768791 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782008 | ATTTTCGGAGCCGGG[C/T]GAGGTGGCTCATGCC | 11060 |
rs371799729 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857566 | AAGGTTTTCTGTTTG[G/T]CCTTATGCTGAGTTT | 11060 |
rs371827581 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821140 | TCAGGCTGTCTTTAG[C/T]GGTCTCTGAAAAGCC | 11060 |
rs371834471 | snp | C/G | 0.000153988 | 0.00877328 | missense | WWP2 | GRCh38.p7 | 16:69934017 | TCAACCCTATGTATT[C/G]TTTATTTGAATATGC | 11060 |
rs371836786 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69912870 | GAGGATCGCTTGAGT[C/G]CAGGAGTTCGAGACT | 11060 |
rs371861695 | snp | A/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850030 | AGGCAAATCTCTGCC[A/G/T]TTGAAGGCAATATTC | 11060 |
rs371865327 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797183 | TAGCTTTGTACTCCA[C/T]GAGTCTTTGGCTTGC | 11060 |
rs371897307 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938981 | TTCGGGCAAAGTACT[A/G]GGCCCCGTGGGTTGC | 11060 |
rs371908110 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897215 | TCAGGTGATCCTCTC[A/G]CTTCAGCCTCTCGAG | 11060 |
rs371947118 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785886 | CCTGTCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 11060 |
rs372011074 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940319 | CTGGACTAGTTCGGC[A/G]AGGAGACTGGCCACT | 11060 |
rs372056717 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894465 | TAAGAACTGAAGGCT[A/G]CTGAAACCTGGGCTG | 11060 |
rs372071166 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870151 | TGTAAAGCGGGGATA[A/C]TAATATTAATCTACC | 11060 |
rs372083781 | snp | A/G | | | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931842 | TGCGCCGCCGGCTCT[A/G]CATCATCATGCGTGG | 11060 |
rs372091856 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783990 | GGCACAAGAATTTAA[C/T]AGCATCAGTTCTCAA | 11060 |
rs372105519 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779327 | TTATATAATGTCAGG[G/T]TGGTATCTTGCTCAT | 11060 |
rs372123218 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878372 | CAGTTTGTAAAAAAT[C/G]ACATAGTGCAACTCA | 11060 |
rs372152222 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771471 | AGGCTGGTCTCGAAA[C/T]CCTGACCTCAAGTGA | 11060 |
rs372182013 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826961 | AAAAAAAAAGGGGGG[A/G]GGGCGGAGAGAATAA | 11060 |
rs372231596 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881893 | AGACAGAGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 11060 |
rs372240674 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907422 | AAGCAAGCATTACCG[C/T]AGAACTGACTGTAGT | 11060 |
rs372242148 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893983 | ACTCTGTCTTTCTAA[C/G]TTTATCTTCTCAACT | 11060 |
rs372246950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867452 | TTGAGTACATTTCAG[C/T]GGCCCTCATGAAGGG | 11060 |
rs372250531 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850197 | TGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 11060 |
rs372295875 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784843 | TGGGTATTTGGCAAG[A/C]CTTTTCTTGAAAACG | 11060 |
rs372297418 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803293 | TTCAGCATGCATCTT[G/T]TTAAAACAGGACATT | 11060 |
rs372318304 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861699 | AAGAATTGAGGGGGG[-/G]TGCAGGTGGGAGTAG | 11060 |
rs372355943 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856793 | ATAAAAAATAAAAAA[A/T]AAATACAACAACAAC | 11060 |
rs372377821 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69881378 | GAATAATAATATCTT[C/T]CTCATAAGGGCATTG | 11060 |
rs372408281 | in-del | -/GACTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908746 | TCTCATGCTACCCTT[-/GACTTT]ATTTTTCAGATGGGA | 11060 |
rs372418153 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819862 | CCCATTTATAGTGAA[C/T]TCCCCTTTCCACCTC | 11060 |
rs372438560 | snp | C/G | 1.64852e-05 | 0.00287094 | missense | WWP2 | GRCh38.p7 | 16:69798756 | GTGGCGGTGGATGGA[C/G]TCCCCAGTGAGACCA | 11060 |
rs372442793 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780270 | CTTTTTTTTTTTTTT[C/T]CCCTCTTGGCATTAT | 11060 |
rs372477547 | snp | G/T | 8.45888e-05 | 0.00650286 | intron-variant | WWP2 | GRCh38.p7 | 16:69871770 | CCTTTTCACAGTGAC[G/T]TATGTCTGTCTGCTT | 11060 |
rs372486204 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826955 | AAAAAAAAAAAAAAA[A/G]GGGGGGGGGCGGAGA | 11060 |
rs372505477 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69939827 | TGACTGTCGTGCTTC[C/T]CCACTCTCAATAGCT | 11060 |
rs372517256 | snp | C/T | 6.59685e-05 | 0.00574281 | missense | WWP2 | GRCh38.p7 | 16:69930243 | TTAAGGATCCTCGCC[C/T]GGGGTTTGAGTCGGG | 11060 |
rs372519122 | in-del | -/CG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822468 | CAGTTGTGACAGATG[-/CG]ATGGAGCAAAGTACA | 11060 |
rs372528208 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838335 | GAACTGTGAATTAAA[C/G]TCGGAGTGCCTGACC | 11060 |
rs372556143 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | WWP2 | GRCh38.p7 | 16:69935199 | CCCTGCCTTCCTGAG[C/T]GTCCCACCCGGCTCC | 11060 |
rs372589501 | snp | C/T | 4.94311e-05 | 0.00497123 | missense | WWP2 | GRCh38.p7 | 16:69888168 | CTGCCCCAGCCACAC[C/T]GGCTGAAGGAGAGGA | 11060 |
rs372615059 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884951 | TGAATTATTTAATTA[C/T]TTAAGCCTATTTCTG | 11060 |
rs372632217 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875341 | CTTCACTGGTGGAAG[A/G]TCTCTCCTCGATGTT | 11060 |
rs372648736 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821849 | AGGCGTGAGCCACCA[C/T]GCCCGGCTATTTTTC | 11060 |
rs372687880 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906289 | GTGTTAGCCAGGATG[A/G]TCTTGATCTCCTGAC | 11060 |
rs372699378 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779257 | TGCGTGGCCCCGGCC[A/G]GTTATTTTTCTTTAT | 11060 |
rs372702013 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850644 | TGTCACTGCAGGCAG[A/T]GGGTACAGCATGAGT | 11060 |
rs372722256 | snp | A/C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817784 | CCACCTCAGCCTTCC[A/C/G]AGTAGCTGAGATTAC | 11060 |
rs372760071 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840466 | CAGTAAATGTCCAGT[C/T]TTTGTAAATATGTAA | 11060 |
rs372780534 | in-del | -/ATGGGAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817144 | CCTTTTTCCCCCCAA[-/ATGGGAA]CTCATTATACATATT | 11060 |
rs372805832 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839161 | TGTTGGATTGGGTGG[A/G]GCGGGTGGGGAGGGA | 11060 |
rs372823811 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804116 | TTATTATTCTTCGTC[C/T]TACCATTTGTAAATG | 11060 |
rs372830305 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900127 | AAATTTTTGACACCT[A/G]ATTATTTCTTTGGGA | 11060 |
rs372830672 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761455 | GTGCACGCCTGTAAT[C/T]CCAGCTACTCGGGAG | 11060 |
rs372832231 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905389 | AGATCAGATCTGAGC[A/G]GAAGATTGTGATTAA | 11060 |
rs372839215 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840689 | ACTAGCAAAATACAG[A/G]CAGAGCAGGGAATTT | 11060 |
rs372845231 | snp | G/T | 1.65285e-05 | 0.00287471 | missense | WWP2 | GRCh38.p7 | 16:69917838 | GTCGCAGCGGAATCA[G/T]CTCCAGGGGGCCATG | 11060 |
rs372849011 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908321 | CTGGAGGGCCTATAG[A/G]TGATCTTGTGGAGGG | 11060 |
rs372851157 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810277 | GTGGCGGATGGTCAA[A/C]CTGGGCTGACTTCTC | 11060 |
rs372934907 | in-del | -/GAGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809806 | AGAGAGAGAGAGAGA[-/GAGA]TAGGAAGGAAGGAAG | 11060 |
rs372944650 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780334 | TATTTCAGGTACTAT[-/T]ATAGCATTCCATTTT | 11060 |
rs372951495 | snp | C/T | 4.94401e-05 | 0.00497168 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931241 | ATGTGAGTTCTGGTA[C/T]TGGGGCTCCCGTGGC | 11060 |
rs373037002 | snp | C/T | 0.000231099 | 0.0107469 | intron-variant | WWP2 | GRCh38.p7 | 16:69936274 | GGAAAGACCCTGACA[C/T]GGTAGACATCTCCCC | 11060 |
rs373059814 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890121 | ACCATGCCTGGATAA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs373060243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903491 | AAAAGAAAAATGGCC[A/G]GGCGCAGTGGCTCAC | 11060 |
rs373088609 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841822 | CCAAGGTTTGAGCCC[C/T]ACTGCTCCATGGCAT | 11060 |
rs373154084 | snp | A/T | 1.651e-05 | 0.0028731 | missense | WWP2 | GRCh38.p7 | 16:69799268 | TCTGTCAACCTCTCC[A/T]ACGTCTTGAAGAACA | 11060 |
rs373155983 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836049 | CTCAGGTGATCCACC[C/T]ACCTCGGCCTCCCAA | 11060 |
rs373156840 | in-del | -/TCAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793674 | TAGATTGCCAGAAAG[-/TCAG]AAAAAATCTCAAAAG | 11060 |
rs373194435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69799730 | TGTGCATGTGTGCAC[A/G]TGTGTGTCTGGGATA | 11060 |
rs373196159 | in-del | -/GGG | | | cds-indel | WWP2 | GRCh38.p7 | 16:69917822 | CTATGAGCAGTGGCA[-/GGG]GTCGCAGCGGAATCA | 11060 |
rs373225712 | snp | C/T | 4.9436e-05 | 0.00497148 | intron-variant | WWP2 | GRCh38.p7 | 16:69840098 | GCATTCTCTTTAGCC[C/T]ATCCATGTTGCCTTT | 11060 |
rs373236996 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912923 | CCAGTCTCTACAAAA[-/C]AAAAAAAAAAAAAAA | 11060 |
rs373243296 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846689 | TTGCGCCACTGCACT[C/G]CAGCTGAGTGATGGA | 11060 |
rs373245634 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775564 | TCTCATGTGTTGTCT[C/G]CTGTTTCCATTAGAG | 11060 |
rs373253557 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817480 | GTCTCGAACTCCTGA[C/T]ATCAAGTGATCCACC | 11060 |
rs373262899 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804112 | AAGGTTATTATTCTT[C/T]GTCTTACCATTTGTA | 11060 |
rs373269270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69782213 | TCTTGAACCCGGGAG[A/G]CAGAGGTTGCAGTGA | 11060 |
rs373269438 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827096 | CTCATGCCTTGTGTC[A/G]TTTCACTTGTTGACA | 11060 |
rs373271635 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814806 | AGCAGCTGTACCTGA[C/G]AGACAGTGTACCCAT | 11060 |
rs373275715 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840084 | TCTTAACTTGGGGTG[C/T]ATTCTCTTTAGCCCA | 11060 |
rs373283855 | in-del | GG/GGG/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890542 | CTGTATGTTATAATT[GG/GGG/T]GGGGGGAACAATGCA | 11060 |
rs373297375 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783009 | GAAGGGCTTTTGTCC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs373331107 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834558 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 11060 |
rs373396891 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927713 | GGGCTGGGAGCAGCC[C/T]CTCCCCTGGAAACCT | 11060 |
rs373426555 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792942 | GTGGCCCTTCTGCCT[C/T]GGCCTCCTAAAGTGT | 11060 |
rs373431709 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69859423 | AGCTAGGCATGGTGG[C/T]GCATGCCTGTCATCC | 11060 |
rs373437966 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766198 | CAAGCCAAAGACCTT[A/G]GAGTCACCCTTGACT | 11060 |
rs373459825 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788587 | ATTATTTCCTTAGGC[A/G]TTTTCTCAAAAGCCA | 11060 |
rs373475591 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821415 | AATCCTGCACCCTGT[C/G]TCACTGAGTGCTGGC | 11060 |
rs373476708 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827790 | GCAGGGACTCTCCCT[C/T]CCCTCGGAGATGAGG | 11060 |
rs373476876 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69788786 | TTTGTCGCTTTGGTC[A/G]CTGTTAACTACCCCA | 11060 |
rs373495757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69929760 | GGGCGGCCCGGCTGG[C/T]GGGTGTTGCTGGTCT | 11060 |
rs373526535 | snp | C/T | 1.68488e-05 | 0.00290243 | intron-variant | WWP2 | GRCh38.p7 | 16:69799318 | TGATGAAGGGGGTGC[C/T]GACGTGATTCTTGGG | 11060 |
rs373546683 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779708 | CCTTAGGAAAGAAAG[-/AG]TCCCAATAGAAGTAA | 11060 |
rs373552408 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858512 | CACAGAGAAGAGGGG[A/G]CGCCCTTTATCACAG | 11060 |
rs373594867 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808458 | CCAGGCTGGGGTGCA[A/G]TGGTGCAATCTTGGC | 11060 |
rs373623066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69762434 | GTGGGCTGGCTGCCT[A/G]CACGGGGCGGGCCGG | 11060 |
rs373628403 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69937257 | AGTGTCTGAGGTTGC[C/T]GGGACCCTGAGCCCC | 11060 |
rs373645682 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69794505 | CTGCACTCCAGCCTG[A/G]GCAGCAGAGGGAGAC | 11060 |
rs373680614 | in-del | -/CCTGTGTGCATG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799711 | GTGTGTGTGTGCATG[-/CCTGTGTGCATG]TGTGCACGTGTGTGT | 11060 |
rs373740114 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794079 | TGCGCCACCACGCCC[A/G]GCTAAGTTTTGTACT | 11060 |
rs373742013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939473 | GATGAGCTCCTGGGA[C/T]AGCCCAGTGGGTGTA | 11060 |
rs373742599 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809551 | GTGGGTGTATCACCT[A/G]AGGTCAGGAGTTCGA | 11060 |
rs373744747 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837948 | GAATGAAGGCTAGGG[C/T]GCGGTGGCTCACTCC | 11060 |
rs373769408 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69821008 | GGCGAGGCTATGGGC[C/T]GAGCCCAGTTCCAGC | 11060 |
rs373785316 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887917 | AAACTTTTTGCTGTC[A/G]CCCAATACATGTAGT | 11060 |
rs373804082 | snp | A/G | 4.95438e-05 | 0.00497689 | intron-variant | WWP2 | GRCh38.p7 | 16:69934147 | AAGGGGGCCCCAGGG[A/G]TCTGCCTAGTTCCCT | 11060 |
rs373806835 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761365 | ATCATTTGAAGTCAG[A/G]TGTTCGAGACCAGAC | 11060 |
rs373810037 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816818 | ACACATGCACACACA[C/T]ATATGTGTAAACTCA | 11060 |
rs373819604 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837521 | CATGGAGAGGAAAAT[A/T]CAGGCTATCTCTCTG | 11060 |
rs373820374 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853265 | GGATGGGCTGATGCA[A/T]TAGGAGTGAGGGGTC | 11060 |
rs373826742 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790122 | CGTGGTGGCAGGCGC[A/G]TGTAATCCCAGCTAC | 11060 |
rs373828978 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69785800 | CCGACAAATTTGTTG[-/T]TTTTTTAGTATAGAT | 11060 |
rs373830086 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829522 | CAGCTCATTGTGCCA[C/G]AGGACCTTTGCACAC | 11060 |
rs373852811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769794 | GGTAGGTATGATTTT[A/G]TGAAATATATATTTA | 11060 |
rs373854242 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773697 | ATGTTGCCTAGACTG[C/G]TCTCGAATTCCTGGG | 11060 |
rs373881497 | in-del | -/TCAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936192 | AGGAGCTGTCCCCTG[-/TCAC]TCACTGTTCAGGATT | 11060 |
rs373886844 | snp | C/T | 1.65581e-05 | 0.00287728 | intron-variant | WWP2 | GRCh38.p7 | 16:69888010 | CTCATTCTTAGTTGA[C/T]CTTTAAAGTATGATT | 11060 |
rs373897134 | snp | C/T | 1.67925e-05 | 0.00289758 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871864 | CGGCGAGCAAAGCCC[C/T]GGTGCTCGGAGCCGG | 11060 |
rs373899365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806439 | TTATAAAGTAAATTG[A/G]TGTGCTTTCCAACTT | 11060 |
rs373902710 | snp | C/T | 0.000233341 | 0.0107989 | intron-variant | WWP2 | GRCh38.p7 | 16:69929556 | GGCTGAGAGGGGGGC[C/T]GGGCTGGGCTGGGTC | 11060 |
rs373918703 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765257 | GTCTTTTTTTTTCCC[A/G]CTTAACCTTGACTTG | 11060 |
rs373922674 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940879 | GTTGAGGTCCCGAGC[A/G]CCACTCCTAGCCTTG | 11060 |
rs373926120 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | WWP2 | GRCh38.p7 | 16:69908736 | CCACTGTGTGTCTCA[C/T]GCTACCCTTGACTTT | 11060 |
rs373940021 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865580 | AAGCAGGCATTTCAA[A/G]GGAGGGAAAGATGAG | 11060 |
rs374006343 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782727 | ATATCACATAAGACA[-/AA]TTCTGTTCGAGTTTG | 11060 |
rs374011489 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854949 | CAGCCTCAACCTCCA[A/T]GGCTCAAGTGATCCT | 11060 |
rs374016466 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69794296 | TTAGGAGGCTGAGGC[A/G]GGTGGATGACTTTGA | 11060 |
rs374023156 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868633 | AATTTTCTCCCTCAA[A/G]CTCTCTGCCCTCAAC | 11060 |
rs374024708 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819194 | TGACTGTTATTGCAA[A/G]GGCCTCTTAATGGGT | 11060 |
rs374029799 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939952 | GTAACCGAGGCCGCC[C/T]CTCCCACGCCCCCCA | 11060 |
rs374067984 | in-del | -/AACAA | 0.0777841 | 0.181223 | intron-variant | WWP2 | GRCh38.p7 | 16:69897913 | ACTCCATCTCAAAAC[-/AACAA]AACAAAACAAAACAA | 11060 |
rs374069767 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | WWP2 | GRCh38.p7 | 16:69917786 | CCACCTGGCAGCGTC[C/T]GACCGCGGAGTACGT | 11060 |
rs374077548 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | WWP2 | GRCh38.p7 | 16:69892119 | CCTAGCCTGGCACAT[A/G]GTGGGACTCCAGGAA | 11060 |
rs374138481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884122 | CTTGGAATATACAAG[C/T]GTATGTATATATATT | 11060 |
rs374146382 | in-del | -/TCC | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69849386 | CTGTCAGCAGGAAAG[-/TCC]TCCTCCCATGCAGTA | 11060 |
rs374161094 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835254 | TGAGGTGGCTAAGAC[G/T]GCTATTTATAACTAA | 11060 |
rs374175194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69790499 | GTGGCAAAGGCAGGA[A/G]AAAATCCATGTAAAA | 11060 |
rs374190973 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814245 | AGGTAACTGTAGCCT[C/T]GAACTCCTGGGCTCA | 11060 |
rs374206232 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800484 | TGCTTTTGGTTAGCA[A/G]AAGTCCTTGTAGAAA | 11060 |
rs374211311 | snp | G/T | 8.36575e-05 | 0.00646697 | intron-variant | WWP2 | GRCh38.p7 | 16:69929568 | GGCCGGGCTGGGCTG[G/T]GTCTCTGTGCAGCTC | 11060 |
rs374230380 | snp | C/T | 0.000275657 | 0.0117368 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933070 | GGCTTCTGGTGTGGC[C/T]GCGCCCTGTGTGTGT | 11060 |
rs374238237 | in-del | -/CAAAAGTGAAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825118 | CAATGACTTCATACA[-/CAAAAGTGAAC]AAGTTTTTCAAAGTG | 11060 |
rs374242897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921783 | TGCAGTATTGAAACA[A/G]ATTATTTTGACTGGG | 11060 |
rs374243095 | snp | A/C/G | 1.6696e-05 | 0.00288924 | intron-variant | WWP2 | GRCh38.p7 | 16:69936473 | TCTCAGGCGCCGGGG[A/C/G]CTCCGCTCCAGGGGT | 11060 |
rs374248930 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888967 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 11060 |
rs374305246 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924829 | AGGTGAGGGCTTGGG[G/T]CATGAATGTGCCCTC | 11060 |
rs374377851 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918162 | TTCATTTCTGCCCCC[-/AC]TTCATTCAAGTCCAT | 11060 |
rs374386332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938716 | CCCCAAAAACCTTAT[A/G]CCCATTAAGCAGTCA | 11060 |
rs374412706 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899490 | ATCCCAGCACTTCGC[A/G]AGGCCGAGGCAGGTG | 11060 |
rs374450870 | snp | A/G | 8.24287e-05 | 0.00641931 | missense | WWP2 | GRCh38.p7 | 16:69936419 | GCGGCGAGAGCATCC[A/G]GGTCACAGAGGAGAA | 11060 |
rs374467215 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835016 | GGATGTGAACAGCAC[G/T]GATGCAGATAGAGCA | 11060 |
rs374510071 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804780 | AAAGTTAACGTAATG[G/T]GGAATTTTCATACTG | 11060 |
rs374517424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930667 | TGGCACCACTGCACT[C/T]CAGCTCAGGTGACAG | 11060 |
rs374560533 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859439 | GCATGCCTGTCATCC[C/T]GGTTACTCAGGAGGC | 11060 |
rs374561432 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893786 | TGACCTCAAGTGATC[C/T]ACCTGCCTCGGCCTC | 11060 |
rs374624270 | snp | C/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942094 | AGGGAGAGTGTTCCA[C/G]GCAGTCATTCATTTG | 11060 |
rs374642480 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913089 | GAGTGCAGTGGCGCA[A/G]TCTCGGCTCACTGCA | 11060 |
rs374643304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69823816 | TGGTAACCTGATTTC[A/G]CAGAAAAGTTTCTTC | 11060 |
rs374644051 | snp | C/T | 0.000313586 | 0.0125178 | intron-variant | WWP2 | GRCh38.p7 | 16:69840272 | ACAGATGGTGAGTGC[C/T]GCCCTGCTCCTCAGG | 11060 |
rs374651943 | in-del | -/ACAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886470 | AAAAAAACCAAACAA[-/ACAA]CTTTCTGGGCCAGGT | 11060 |
rs374702444 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912271 | CACTCTAGCCTGGAC[A/G]ACAGAGCGAGACTCC | 11060 |
rs374707454 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69896682 | AACAGTTAACAAACA[A/C]CCCCCCAGAGCTGAC | 11060 |
rs374730088 | in-del | -/TGTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862073 | TGTTTTGTTTTGTTT[-/TGTTT]GTTTGTTTTGAGACA | 11060 |
rs374738997 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842990 | TTATTCTTTTTTATG[A/G]TTGTGAAAGAATTCA | 11060 |
rs374767467 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873098 | CGCTGAGATAGTTTT[C/T]TAGTGCTCGTGACAG | 11060 |
rs374780944 | snp | C/G/T | 0.00518061 | 0.050666 | intron-variant | WWP2 | GRCh38.p7 | 16:69850285 | CCAGCTACTCGGGAG[C/G/T]CTGAGGCAGGAGAAT | 11060 |
rs374786839 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905785 | TCCTTATAAATTTCA[A/G]TTCATCTTCCTTTTC | 11060 |
rs374796164 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782969 | AGCCACTGTGCCTCT[C/T]CTGTAACTATATTTA | 11060 |
rs374800347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69810513 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 11060 |
rs374816599 | snp | A/C | 1.6674e-05 | 0.00288734 | intron-variant | WWP2 | GRCh38.p7 | 16:69930296 | AGCAGTGTCAGGAGC[A/C]GAGGCCCAGGCTGTC | 11060 |
rs374819568 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820826 | TGAATACATGCATAT[-/AC]ACACACACACACACA | 11060 |
rs374857599 | snp | C/G/T | 1.64798e-05 | 0.00287047 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931242 | TGTGAGTTCTGGTAC[C/G/T]GGGGCTCCCGTGGCA | 11060 |
rs374904108 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909195 | ATCCAAAACCAAAGG[A/G]TGAGAGAGGCTTCCA | 11060 |
rs374923286 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | WWP2 | GRCh38.p7 | 16:69786955 | CTCCTCTGTCTTCTT[A/G]TCAGATATTCTCTGA | 11060 |
rs374929875 | snp | A/G | 0.000280544 | 0.0118403 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931618 | CAGTGGCAGGCCGAC[A/G]CCCTCCTCCCAGCAC | 11060 |
rs374940578 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820439 | AGTAGAGATGGGATT[A/T]CACCATGTTGGCCAG | 11060 |
rs374941648 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894288 | GTCTCACTCTGTTGC[C/T]CATGCGGATCTCAAA | 11060 |
rs374941801 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916483 | GTTACTCTGATGGCT[A/G]TTTGTAGGCTGGATG | 11060 |
rs374954366 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883152 | GGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 11060 |
rs375011236 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69886557 | TTGAGGCCAGGAGTT[C/T]GAGACCAACCTGGCC | 11060 |
rs375031014 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893297 | TGCACACCAAGGTGG[C/T]CGGGAGCCTGGCACA | 11060 |
rs375046867 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822524 | GAGACTTTGCCTGGC[A/C]TGGGTGGGGTGTGTG | 11060 |
rs375048071 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823786 | AATTTTTGTTAAAAC[A/G]TCACCTTGTCTTCAG | 11060 |
rs375052919 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914651 | AGTCCTAGCTACTTG[G/T]GAGGCTGAGGTGGGA | 11060 |
rs375059518 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860217 | AAAGGAGTCGGGGAG[A/G]TGATGAGTGACTGGA | 11060 |
rs375074200 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69787120 | CATCTTGTCTACGCC[C/G]AGGGAAGAGGGAGAA | 11060 |
rs375087502 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920320 | TGTCTAGCCCAGTGC[A/G]CTCTGCACACTTTCT | 11060 |
rs375095522 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782080 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC | 11060 |
rs375114819 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69808995 | ATAAATTTTACTGTG[C/T]TCTGATCGTTTGTAA | 11060 |
rs375139201 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846214 | TTATATCATAAATTG[A/T]CATACACTCTTATAA | 11060 |
rs375142398 | snp | A/C | 4.98194e-05 | 0.00499071 | intron-variant | WWP2 | GRCh38.p7 | 16:69887995 | AGTATAAATAAAATT[A/C]TCATTCTTAGTTGAT | 11060 |
rs375196352 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897355 | CAATCTGCTCCCCTA[A/G]ACTTCCCAAAGTGCT | 11060 |
rs375209883 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850065 | GATATACATGAATGC[C/T]AGGCTCTGAGCTGTC | 11060 |
rs375217884 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890624 | CTGTTTGTTTTCTTT[A/C]CGCTGAGCGAATGCC | 11060 |
rs375220060 | snp | C/T | 0.000437904 | 0.0147905 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940836 | GCCTGGCAGGGACCT[C/T]GTCCCCAAGCCTGGC | 11060 |
rs375223016 | in-del | -/TC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862707 | CAGCCAGCCATGAAT[-/TC]TTTTTTTTTTTTTTT | 11060 |
rs375225425 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797429 | AGAGTGGGAGAGTGA[C/T]CTTGCCTCTCAAGCC | 11060 |
rs375232061 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809958 | TCTTGGTGTGGAACA[A/G]TGTTTGCAGAGTGGT | 11060 |
rs375253050 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872528 | CCTTTCTATTCATTT[C/T]TTATCTGCATTGGAT | 11060 |
rs375270394 | snp | C/T | 1.65089e-05 | 0.00287301 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931501 | TTCTTTTCTTTTTTT[C/T]TTTTCAGTCAAATGC | 11060 |
rs375272256 | snp | A/G | 0.000531526 | 0.0162936 | missense | WWP2 | GRCh38.p7 | 16:69799290 | TGAAGAACAATGGGG[A/G]CAAAAGTACGTATGA | 11060 |
rs375318503 | snp | C/T | 4.99663e-05 | 0.00499806 | missense | WWP2 | GRCh38.p7 | 16:69799182 | TTTTCAGGAATGTCA[C/T]GGCACAGAGTCATTT | 11060 |
rs375342690 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69796162 | TTAAAAAATGTGTTT[G/T]TTGGGAAATACACCC | 11060 |
rs375361339 | snp | A/G | 1.71905e-05 | 0.00293172 | intron-variant | WWP2 | GRCh38.p7 | 16:69917660 | TTTCTAGAATTGGGG[A/G]ATGGGAGTGGGGTGG | 11060 |
rs375366377 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846865 | TTCTTTGCCTGGGTG[C/G]TGGCTCCCAAGTGTT | 11060 |
rs375373615 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875860 | AGCTTCTTCCAAACT[C/T]CTGTTGTGTTGATAT | 11060 |
rs375380380 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908855 | CTTCCTCCAGGGTAG[A/G]TCATCAACTGAGAAG | 11060 |
rs375380628 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862354 | ACAGGCGTGAGCTAC[C/T]GCGCCTGGCCCTTGT | 11060 |
rs375393099 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827226 | CATAATCTTACTGCT[C/G]AAACACAACTTATCA | 11060 |
rs375396780 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940782 | CAGGAACCCACCTGG[C/T]GGTTCCGTGAGCTCA | 11060 |
rs375413528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846364 | TCATACGTAGAAAGT[A/T]GAAAAATGCAAAGCC | 11060 |
rs375433844 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69939796 | TGGGGCTATCAGAGC[C/G]CTGGCCTCCTAGGGC | 11060 |
rs375465226 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908586 | TCTTCAAGAAGCACT[C/G]CTGGCTGGCACCCTC | 11060 |
rs375487224 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876658 | CGTGAGCCACTGTGC[C/G]CAGCCATAAAATGTA | 11060 |
rs375492553 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778192 | TATATATATATATAT[-/A]TTTTTTTTTTTTTGA | 11060 |
rs375528053 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803618 | CAAATTTGTTAAGAA[A/G]GTAAAGGAAGGCAGG | 11060 |
rs375557351 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882040 | GACCAAGCTGGTCTC[A/G]AACTCCTGGCTTCAA | 11060 |
rs375590054 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858650 | TTGAATGCTTTTCAC[C/T]GACTGTTCTTTTCAA | 11060 |
rs375594780 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826962 | AAAAAAAAGGGGGGG[G/T]GGCGGAGAGAATAAT | 11060 |
rs375618808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69853343 | ACATGCCAAGAAACT[A/G]CTGTGCCCTTGCAAC | 11060 |
rs375622575 | snp | C/T | 1.67894e-05 | 0.00289731 | intron-variant | WWP2 | GRCh38.p7 | 16:69929434 | GATGTTCTTTCTTTC[C/T]TCTCATGTGGCAGAG | 11060 |
rs375624215 | in-del | -/GTGCAGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868939 | GTTGTCCAGGCTGGA[-/GTGCAGT]GGTACAATCTCGGCT | 11060 |
rs375631034 | snp | A/G | 1.65971e-05 | 0.00288067 | intron-variant | WWP2 | GRCh38.p7 | 16:69937501 | TAGCGAGTGGACGAT[A/G]CGCGGGGAGGGACCT | 11060 |
rs375640664 | snp | A/G | 1.7072e-05 | 0.00292159 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931921 | CCGGAAGGCTGCCCT[A/G]TACCCCGCTTCCCCA | 11060 |
rs375643484 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840160 | CCTGAACCTGCAGAC[A/G]GAGAACAAAGGCAGC | 11060 |
rs375644118 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774274 | CAGCATTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 11060 |
rs375663821 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69937079 | CCACCCCTGAGCAGT[A/G]GGTCTCAGACTCCAC | 11060 |
rs375698966 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911396 | AGGGAAGTGGCTCCA[A/G]CTCTTGCAAGAAGAT | 11060 |
rs375704254 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904456 | TCACTGCAGCCTCCA[A/G]CTCCTGGGCTCAAGT | 11060 |
rs375710798 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879256 | AAACCATTTTTAGGT[A/G]TGTAATTCAGTGGCA | 11060 |
rs375714295 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891629 | GACTGTTTCATGATG[C/T]GTGCCCTGGTCACTC | 11060 |
rs375722438 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69895858 | CCATTCTTTGAGTAG[C/T]ATCAGATTAAAGGAT | 11060 |
rs375725178 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69788628 | GATCCCCTGATCCAA[C/T]GCCACCTTTCTCATT | 11060 |
rs375745141 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775913 | CTGTGTTTAATGATT[G/T]CTGTAACTGTTGGTA | 11060 |
rs375763288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863635 | GAAAGAGTGAAACTC[C/T]GTCTCAAAAACAAAC | 11060 |
rs375792321 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925150 | CGCCACCCTGGCACA[-/C]CTTCACCCGCGTACC | 11060 |
rs375794420 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69807891 | TTCAGTCTGGGAGAT[A/G]GAGGCTGCAGTAAGC | 11060 |
rs375796894 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817808 | AGATTACAGGCTTGT[A/G]TCACCATGCTTGGCT | 11060 |
rs375803034 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932352 | AAAACAAACAAAAAA[A/G]CAAAATACGTGAATC | 11060 |
rs375821404 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761836 | GGCACATAATAGGCA[C/T]AAGGTTGCCAGGAAA | 11060 |
rs375843246 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784955 | AGAAAAGAAAGAGTG[C/G]TCGAGTGCAGTGGTT | 11060 |
rs375848914 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820471 | CTGGTCTTGAAATCC[C/T]GATCTTAAGTGATCC | 11060 |
rs375884973 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892982 | CCCACCTACCCTTCA[A/T]GCCTTCGGTGGGATC | 11060 |
rs375885473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870441 | GAGTAGCTGGGACTA[C/T]AGGCATGCACCGGTA | 11060 |
rs375899073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69901858 | CGGGAGGCTGAGGCA[A/G]GAGCATCACTTGAAC | 11060 |
rs375953524 | snp | G/T | 4.95323e-05 | 0.00497631 | intron-variant | WWP2 | GRCh38.p7 | 16:69930124 | CTTTTCTTCCCGTGT[G/T]TCCAGGATGATCCAG | 11060 |
rs375955183 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782370 | GAACATTGATTGCTT[G/T]AGGTTGAGGACGGGG | 11060 |
rs376007962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69925552 | CTGTCCTCTCCTCCC[A/G]CGTGTCTTCCTTCCC | 11060 |
rs376046389 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915075 | CACACAACTGTCCCC[A/G]TCAGATGAGGGAGAG | 11060 |
rs376107408 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883485 | GAGTATTCGTGGGCA[C/G]AGAAGGCTTGTCCAT | 11060 |
rs376111389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861111 | GCTCATCTCCTAAGC[A/G]GCAACAGTGTCCTAT | 11060 |
rs376128021 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69778498 | AGACAGAGTGTGAAG[A/T]CTGGGCCTCAGGTTT | 11060 |
rs376129571 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836055 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs376173136 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890251 | GACCTTTACTACGTA[C/T]GTATTGTTTTCCTAG | 11060 |
rs376188375 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830790 | ACAGTAAATCCTGGA[A/G]TCATCTGGCTTCCTT | 11060 |
rs376210232 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776325 | TGGTTACTTCCCACA[A/G]CTAGAGCTAGGAGGG | 11060 |
rs376239111 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783211 | GATGGGGTTTCATCA[C/T]ATTGGCCGGGTTGGT | 11060 |
rs376248829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69825087 | AGCTTTTATGTGTAT[A/G]TTTGTGCTTGTGTTT | 11060 |
rs376257136 | snp | A/C/T | 0.00015291 | 0.00874262 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939919 | TGCCATTGAGGAGAC[A/C/T]GAGGGCTTTGGACAG | 11060 |
rs376291756 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69820547 | CCGCTCTTGGCCCCC[-/T]GTCTCTTAAAAAAAA | 11060 |
rs376315106 | in-del | -/GTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893561 | AATGCTGTTTTTTTT[-/GTT]TGTTTGTTTTTGTTT | 11060 |
rs376411654 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840768 | GATCTAGTCTGAAAT[C/T]AGTCACCTTTGGATC | 11060 |
rs376424183 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868205 | GGTGGTGGCTGGCCA[C/T]GGGCAGGGAGGTGGC | 11060 |
rs376430499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69796928 | TTTGCCAAGTTGTAG[A/G]CACCATTGTAGGACT | 11060 |
rs376453245 | in-del | -/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845914 | AATTAGCCAGGCATG[-/GT]GGTGTGTGCCTATAA | 11060 |
rs376455893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929689 | CGTACAGATACACTG[C/T]TGGCCTGATGAGAGC | 11060 |
rs376471201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848755 | GCATGTGAACGCACA[A/T]GAGAGAGTGTGTATG | 11060 |
rs376477766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813224 | CTGGAGTGCAATGGC[A/G]CGATCTTCGCTCACC | 11060 |
rs376485182 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897541 | TGGGACATGCATTTA[A/G]ACTGCTATACGGTGT | 11060 |
rs376493642 | snp | A/G | 0.000153988 | 0.00877327 | splice-acceptor-variant | WWP2 | GRCh38.p7 | 16:69871802 | CTACTTTGAACCCCC[A/G]GGACGCACAGACATT | 11060 |
rs376501108 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935243 | CCCAAGCGCCCCATG[A/G]GCCTGTGACTAAATA | 11060 |
rs376502073 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69937255 | TGAGTGTCTGAGGTT[G/T]CTGGGACCCTGAGCC | 11060 |
rs376502752 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766199 | AAGCCAAAGACCTTG[A/G]AGTCACCCTTGACTC | 11060 |
rs376505165 | snp | C/G/T | 8.95847e-05 | 0.00669218 | intron-variant | WWP2 | GRCh38.p7 | 16:69917917 | GGCCCGAGGTGGGGC[C/G/T]GCCTCCCTGCGCTTG | 11060 |
rs376524877 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801182 | GACAGAGCAAGTCTT[-/A]AAAAAAAAAAAAAAA | 11060 |
rs376532142 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873999 | AGGCAGGTGCCAGCC[A/G]TGTCTTCAAAAGCCA | 11060 |
rs376536260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69843935 | GAAAAATGGAATATG[A/G]TTTTAGCCAATACCC | 11060 |
rs376554965 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841937 | ACTCTAACACACAGA[C/T]GGAGTTCTGTTCCTG | 11060 |
rs376590618 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906748 | AGCTGGGCCTCGTGG[C/T]ATGCACTTGTTTTCC | 11060 |
rs376594037 | snp | C/T | 4.9476e-05 | 0.00497348 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917799 | TCCGACCGCGGAGTA[C/T]GTGCGCAACTATGAG | 11060 |
rs376620650 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826724 | CTCTAATAAAAATAC[-/AA]AAAAAAAAAAAAAAA | 11060 |
rs376626363 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813713 | GGCTCTAGTGATCCT[C/G]CCACGTTGGCGTCCC | 11060 |
rs376631814 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864166 | TGATCTCAGGAGTTC[A/G]ATATCAGCCTGGGCA | 11060 |
rs376631971 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837038 | AGGTGATTCTCCCAC[C/G]TCTGCCTCCTCAGTA | 11060 |
rs376633436 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816648 | TATTCTGAGTGCTTC[A/G]TATGTATCAGTCATT | 11060 |
rs376648616 | snp | C/T | 0.00019998 | 0.0099975 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933201 | CGTCGACGGACTCCT[C/T]GTCTGCCCAGCCACA | 11060 |
rs376654911 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793344 | GTGACAGAGCAAGAC[G/T]CCATCTAAAAAAATA | 11060 |
rs376659549 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845143 | CCCAGTTTTTTTCAG[A/G]TGTAAAGTGGGGGTA | 11060 |
rs376660611 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773752 | CTCCCAAAGTGCTTG[G/T]ATTACAGGCATGAGC | 11060 |
rs376665756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69796260 | TATGTGTATGAGCGC[A/G]GATACTTCTCAACTT | 11060 |
rs376684629 | in-del | -/CT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857653 | GCCTTTGAAGGTCAA[-/CT]CTTTTTTTTTTTTTT | 11060 |
rs376710523 | snp | C/G | 0.000153988 | 0.00877328 | missense | WWP2 | GRCh38.p7 | 16:69939357 | TAGCAACGGACCACA[C/G]AAGTTTTGCATTGAC | 11060 |
rs376739130 | in-del | -/CACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912370 | GCAGGGAGTTAGATT[-/CACACA]CACACACACACACAC | 11060 |
rs376753742 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817628 | TTTCTATTGTTTTTT[-/T]ACAATTACTAGCAGC | 11060 |
rs376797337 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873556 | TGTGCTGGAACATCC[A/G]GTGGTAGCTGAGCCT | 11060 |
rs376811434 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821202 | TCAGGCAGATATGCC[C/T]AGGCCAGAACCTCAA | 11060 |
rs376816165 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841535 | CTCAGATCACGCAGC[C/G]TTGAAACATTTGGTA | 11060 |
rs376889803 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906293 | TAGCCAGGATGATCT[C/T]GATCTCCTGACCTTG | 11060 |
rs376904259 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69886220 | GAGTAGCTGGGACCA[-/C]AGGTGGGCACCACCA | 11060 |
rs376923495 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794110 | TGTAGTAGAGACGGG[G/T]TTTCACCAAGTTGGC | 11060 |
rs376924489 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838096 | ACAAAAAACAAATAC[A/G]GTGAATGAGAAGTTA | 11060 |
rs376955324 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871052 | GCACTTTGGGAGGCT[A/G]AGGTGGGAGGATCGT | 11060 |
rs376958344 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888310 | TGAGGCTCCTTTACG[A/G]GGGTGGAAACAACGT | 11060 |
rs376989376 | in-del | -/AG | 0.356383 | 0.226236 | intron-variant | WWP2 | GRCh38.p7 | 16:69820427 | TTTTGTATTTTTAGT[-/AG]AGATGGGATTTCACC | 11060 |
rs377006918 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872256 | GAGTCTCACCCTGTC[A/G]CCCAGGCTGGAGTGC | 11060 |
rs377013508 | in-del | -/T | 0.296364 | 0.245663 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760497 | CATGCCCGGCGAATC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs377027568 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840729 | CCCTTGCTCTGTCCC[A/G]AATGTTGGTAGTTTG | 11060 |
rs377034951 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761095 | CCTGCCTGGGCTACA[A/G]GAGTGAAACTCTGTC | 11060 |
rs377056658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906552 | TAGCTCTGCTATAAC[A/T]TATGTGCTCCTAAAA | 11060 |
rs377062044 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772541 | CTCCTGCAGAGCAGG[G/T]CTACGCTATAGGCAG | 11060 |
rs377065935 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896728 | TGCAGCTTGTGTGTA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs377082894 | in-del | -/AAGTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780392 | CATTGATGGGTATTT[-/AAGTT]GTTTATAATTTTTTA | 11060 |
rs377141047 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882079 | CCTGCTTTGGCCTCC[A/G]AAAGTACTGGGATTA | 11060 |
rs377153304 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795276 | CACACACACACACAC[-/A]CACACACACACACAC | 11060 |
rs377213284 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826956 | AAAAAAAAAAAAAAG[A/G]GGGGGGGGCGGAGAG | 11060 |
rs377229472 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925596 | CTGTTTTCCATCTCT[C/T]CCCTCTCCAGCACAC | 11060 |
rs377246940 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829596 | ACCCTGCTAGCTGTC[G/T]TCTTGAAACTTAGAT | 11060 |
rs377273614 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793569 | TGAGATTATAGAGGT[A/G]TGGAAAATGGTCCTG | 11060 |
rs377275994 | snp | C/T | 0.000148816 | 0.00862471 | utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69787001 | TGTCTTACAGCTTCA[C/T]GGTGATGATATGGCA | 11060 |
rs377277535 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769874 | CCAAGTGATCAGTGT[-/C]TTTTTTTTTTTTTTT | 11060 |
rs377346036 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908069 | AACATGGTGAAACCC[A/G]TCTCTACCAAAAATT | 11060 |
rs377349940 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937443 | TTATTAACGCTGACA[A/C]CAAAAATAGCTAGTT | 11060 |
rs377368097 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769028 | CATATCTTTCAAGAA[A/T]TGAGTGCAGGCTGGG | 11060 |
rs377377176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69810259 | TTTCACTCACGTCCC[G/T]CAGTGGCGGATGGTC | 11060 |
rs377409611 | snp | C/T | 6.59337e-05 | 0.0057413 | intron-variant | WWP2 | GRCh38.p7 | 16:69925500 | GTAAGTACTGAGTTC[C/T]CTTCCTGGCCCTTGG | 11060 |
rs377422202 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69832239 | CAGAGGTGGAAAAAC[-/A]GTCGATGAATCCCCA | 11060 |
rs377456249 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912027 | GGGCTCGGTTGCTCA[C/T]GCCTGTAATCCCAGC | 11060 |
rs377470408 | snp | C/T | 1.80928e-05 | 0.00300767 | intron-variant | WWP2 | GRCh38.p7 | 16:69888261 | CTGGGTGAGTAGTCT[C/T]CTGTCCCATAACAGA | 11060 |
rs377471067 | in-del | -/TGG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845912 | AAAATTAGCCAGGCA[-/TGG]TGGTGTGTGCCTATA | 11060 |
rs377529775 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811395 | GAGGTTTGCTTGAGC[A/G]TGGGAGTTCAAGACC | 11060 |
rs377545276 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919212 | CTCTTGTTGCCCAAG[C/G]TGGAGTGCAATGGCA | 11060 |
rs377569189 | snp | A/G | 0.000437904 | 0.0147905 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940265 | TGTGCAAGGGAAGGT[A/G]TTGCATCCCCAGGGG | 11060 |
rs377573067 | snp | A/G | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, missense | WWP2 | GRCh38.p7 | 16:69840127 | TTTGTACCCCACAGT[A/G]GAGAACATGCAGCTG | 11060 |
rs377606984 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798646 | ATCTGGGAGCCCTGG[G/T]ACTCATCTTTGACTT | 11060 |
rs377607485 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817162 | GGAACTCATTATACA[C/T]ATTTCTTTGTAACTT | 11060 |
rs377611042 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807111 | TTGGCTCACTGCAAC[C/T]TCTGCCTCCTGGTTT | 11060 |
rs377611927 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784749 | GCACGGTTGTTTGAA[C/T]TGAGAGCTGAATTAA | 11060 |
rs377619443 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | WWP2 | GRCh38.p7 | 16:69908789 | GAGCTGCCCAACGGA[C/T]GTGTCTATTATGTTG | 11060 |
rs377626174 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | WWP2 | GRCh38.p7 | 16:69936306 | CTTGGTCTCCTGTGC[A/C]CCCAGAGAGAACAAC | 11060 |
rs377655113 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924883 | CAGATGGGAGGTTGG[A/G]GGGGACGCCGAGGTG | 11060 |
rs377659131 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812412 | TCAGGTAACCTGCCC[A/G]CCTCGGCCTCCCAAA | 11060 |
rs377668326 | snp | C/T | 1.71858e-05 | 0.00293132 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931927 | GGCTGCCCTGTACCC[C/T]GCTTCCCCAGGCTAC | 11060 |
rs377668595 | snp | C/T | 6.58946e-05 | 0.0057396 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840187 | CAGCGTTGTCTCAGG[C/T]GGAGAGCTGACAATT | 11060 |
rs377703472 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903422 | CAAATGAACATAAAA[G/T]ATGTCAAAAGTGGAG | 11060 |
rs377705388 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879625 | TCCATTCATCTGTAG[A/G]TGGACATTTGGGTTG | 11060 |
rs377708325 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830184 | GGTCTTGAACTCCAG[C/T]GCTCAGGCGATCTCT | 11060 |
rs377749970 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916944 | CGAGGTGGGAGGATC[A/G]TTTGAGTCCAGGAGT | 11060 |
rs377758808 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841332 | TCTCATCTAAGTTGC[A/G]GGGTCAGGGAAGGTT | 11060 |
rs386384998 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795650 | TTAAAAATAGGAGGT[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs386791844 | multinucleotide-polymorphism | CAC/TAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795261 | AAAAAAATGCGGATA[CAC/TAT]ACACACACACACACA | 11060 |
rs386791845 | multinucleotide-polymorphism | AA/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804756 | ATTTTATGGAGTCCT[AA/GT]CATATGTAAAGTTAA | 11060 |
rs386791847 | in-del | ATGGT/CAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845911 | AAAAATTAGCCAGGC[ATGGT/CAC]GGTGTGTGCCTATAA | 11060 |
rs386791848 | multinucleotide-polymorphism | ACG/GCA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851261 | GGACTCAAGTGATCC[ACG/GCA]TGCCTTGGCCCTCAC | 11060 |
rs386791849 | multinucleotide-polymorphism | ATT/GTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853369 | GCAACCGCTTTATGT[ATT/GTA]TGAAGTGGGTGTGCA | 11060 |
rs386791850 | multinucleotide-polymorphism | GC/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854463 | TTTGGTTTAGTGACT[GC/TT]CTTTCTGGTGGCATT | 11060 |
rs386791851 | multinucleotide-polymorphism | CA/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870538 | ACTCCTGGGCTCAAG[CA/TG]ATCCTCCCGCCTTGG | 11060 |
rs386791852 | in-del | C/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897104 | CCCGTCTTTTTTTTT[C/TT]GTTTGTGTGTTTTGT | 11060 |
rs386791853 | multinucleotide-polymorphism | ACT/GCG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927089 | GTGGTCAGAGTCGAT[ACT/GCG]GTTAATGAACGATCA | 11060 |
rs386791854 | multinucleotide-polymorphism | CT/TG | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931377 | GCTGTCTCTAGGAAG[CT/TG]AGTTTTCATTCCTAG | 11060 |
rs386791855 | multinucleotide-polymorphism | CG/TA | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932071 | GCGGTGGCTCACGCC[CG/TA]TAATCCCAGCACTTT | 11060 |
rs397728126 | in-del | -/CT/TG/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785224 | TAGGTGTGTGAGACT[-/CT/TG/TT]GTCTCAAAAAAAAAA | 11060 |
rs397736218 | in-del | -/A | 0 | 0 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761589 | AAAAAAAAAAAAAAA[-/A]TATCATCTATCTATC | 11060 |
rs397785683 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923428 | GCTGAGATTTTTTTT[-/T]AAAAGGCAAGGATTC | 11060 |
rs397786044 | in-del | -/TGTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927441 | GACCCTGGGCCTGTG[-/TGTG]GCTGAATATGTCTGA | 11060 |
rs397798000 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851833 | AAATACAAAAAAAAA[-/A]TTAGCTGGGCGTGGT | 11060 |
rs397830599 | in-del | -/TTCATTCATTCA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849515 | TCATTCATTCATTCA[-/TTCATTCATTCA]GTTATAATTAAGACA | 11060 |
rs397934680 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860853 | TTAAAAAAAAAAAAA[-/A]GGAAAGAAAGAACAC | 11060 |
rs397942280 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770986 | AAAAAAAAAAAAAAA[-/A]GGTAGTATTCTGTGT | 11060 |
rs397951339 | in-del | -/TATTCATTCATTCATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849485 | ATTTATTTATTTATT[-/TATTCATTCATTCATT]CATTCATTCATTCAT | 11060 |
rs397958228 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803349 | TTCTATTTTTTTTTT[-/T]ACTTTGGAACATTTA | 11060 |
rs397960310 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829972 | TTTTTTTTTTTTTTT[-/T]CAGATAGAGTCTAAC | 11060 |
rs397971883 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778205 | TATTTTTTTTTTTTT[-/TTT]GAGAAATTTCAATAG | 11060 |
rs398029837 | in-del | -/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69769892 | TTTTTTTTTTTTTTT[-/T]GAGATAGAATCTCGC | 11060 |
rs398029838 | in-del | -/A | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69826282 | CAAAAAAAAAAAAAA[-/A]GTAGACCAGGCGCAG | 11060 |
rs398041992 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69784096 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 11060 |
rs398042208 | in-del | -/CA | 0.5 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69883401 | TTCTAAGAATGTGCG[-/CA]CACACACACACACAC | 11060 |
rs398058352 | in-del | -/CACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868686 | ACACACACACACACA[-/CACACACA]GACATACACACACAG | 11060 |
rs398070839 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827441 | TTTCCATGTTGTTGT[-/TGT]ATACGCTTTATAATC | 11060 |
rs398119475 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827166 | ATGAAAAAAAAAAAA[-/A]CTACTGTGGAATTAA | 11060 |
rs398119476 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913210 | TGTAATTTTTTTTTT[-/T]AAAGTAGAGATGGGG | 11060 |
rs527238328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849723 | TGAGGCAGAAGGATC[A/G]CTTGAGGCCAGGAGT | 11060 |
rs527253777 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939500 | TGTAGCAGCTTCATA[A/G]CCTCGAGTCTGGCAG | 11060 |
rs527276566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859993 | GGCATTGGAGGGGGG[C/T]TAGAGTGAGAGGGAT | 11060 |
rs527278736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889935 | TCCCATCTCTTTATT[C/G]TATTATTAAGCCACT | 11060 |
rs527297990 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69843932 | TTTGAAAAATGGAAT[A/C]TGATTTTAGCCAATA | 11060 |
rs527309753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69935470 | CCACCCACCCTGAGC[A/G]CCAGTGAATCAGGGC | 11060 |
rs527319187 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929490 | ATTACGTGAACCATA[A/G]CACTCGCACGACCCA | 11060 |
rs527328918 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886911 | TTCTGCATTAGGAAG[A/C]TGAGGCTAAATGATG | 11060 |
rs527349170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895096 | CCCAATTATGGATAT[A/C]CAGAGGCACTCTCTT | 11060 |
rs527354715 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69844749 | AGGTACCTTCCGATA[C/G]TGTAAGCCTTATCGG | 11060 |
rs527361952 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794020 | CCTCCTGGGTTCAAG[C/T]GATTCTCGTGTCTTA | 11060 |
rs527372098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764573 | ACAGAAAAAGTTGTG[A/G]ATGTAGAATGTGAGT | 11060 |
rs527405929 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936804 | CTCACGTGTGCCCGT[A/T]CTCCGTGCCTGTTCC | 11060 |
rs527422942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808497 | ACCTCCACCTCCCAG[C/G]TTCAAGCAGTTCTCC | 11060 |
rs527439682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922454 | CAGATCTCCCAACCC[A/G]GGGACCATTACCCGG | 11060 |
rs527446873 | in-del | -/ATTC | 0.23169 | 0.249329 | intron-variant | WWP2 | GRCh38.p7 | 16:69806957 | TTTATTTATTTATTC[-/ATTC]ATTCATTCATTCATT | 11060 |
rs527447121 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872842 | GAGACGGGAAGGACC[C/T]ATTTCAAAACAACTC | 11060 |
rs527460794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877676 | TGATTTAAAGTGAGA[A/G]ACATATGACTCTTCC | 11060 |
rs527474504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788407 | AGTAGAAGCCGAAGC[G/T]CCCATGTGATGTGAC | 11060 |
rs527488053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69780933 | CTCAGGAATCTGAGG[C/T]GGAAGGATCACTGGA | 11060 |
rs527496729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915417 | GCAAATATGGCAAAA[A/G]TCAAGAAATAATGAG | 11060 |
rs527512187 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850345 | TGAGCCGAGATCACA[C/G]CACTGCACTCCAGCC | 11060 |
rs527515988 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824880 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 11060 |
rs527522022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870787 | TGGTGAAACAGATGA[A/G]CCGAAGGACAGGGAG | 11060 |
rs527532062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890444 | CAATTGCTTTGTGTC[C/T]AGCTACTCCCTATAG | 11060 |
rs527544415 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69883553 | ATCTGAACTCAAGGT[A/G]TAGCACAAACTTTCT | 11060 |
rs527549411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794333 | GCTTAAAGTTTGAGA[C/T]CAGCCTGGGCAACAT | 11060 |
rs527556601 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786925 | TTTAAGCTTAAATAT[G/T]GAAATTGAGTTAAAC | 11060 |
rs527569197 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917061 | AAAGACCATGCAACA[C/T]GTTTACACTGGCACC | 11060 |
rs527574327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921827 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG | 11060 |
rs527586515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69794986 | TTGGAAAGCTCTGGC[A/G]GGTAGATCGCTTGAG | 11060 |
rs527588152 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836835 | TGCCCAGGATGGTCT[C/T]GAATTCCTGAGCTCA | 11060 |
rs527595694 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791625 | ATAGGCTCAAGCAAT[A/C/T]CTCCTGCCTCAGCCT | 11060 |
rs527596362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69787930 | CAGCCACTTCTCACC[A/G]CCCCTAGGTCCCAGC | 11060 |
rs527625662 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69829098 | GCCGTCTTCGATACC[C/T]GACCCCTCTTGCCCA | 11060 |
rs527632048 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896398 | AGTGCTGGGGTTACA[A/G]GTGTGAACCACCGTG | 11060 |
rs527638862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920319 | CTGTCTAGCCCAGTG[C/T]GCTCTGCACACTTTC | 11060 |
rs527639488 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865676 | AATATTTATGAAGGG[A/G]ACACACATGCATGTG | 11060 |
rs527640473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928636 | TAGGCAGGCCAGGCA[C/T]GGTGGCTTATTGCCT | 11060 |
rs527663554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882642 | GTGCTTTCCCTGGGC[C/T]GCAGGGGTCGGGAGG | 11060 |
rs527681448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69785930 | ACTGCACCCAGCCTA[C/T]CCATTTAAATAATTG | 11060 |
rs527703004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920833 | GCAATTTTTTTTTCC[C/T]TTAAAAGCCCCACTA | 11060 |
rs527710485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835664 | GCCATTTGAAGGTAA[A/G]TTGCAGATATCATGA | 11060 |
rs527736319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69888347 | TTATTACCTAGTGGC[C/T]AGTAGCCTCTGGGGA | 11060 |
rs527778007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927780 | GGTAGCTCTGTAACA[C/G]CTCTGGGCACCTCCT | 11060 |
rs527829805 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940925 | AAGAAATCCCTTTGC[C/T]AGATAGGGTCCCCCA | 11060 |
rs527879710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848241 | GGATCACCTGAGGTC[A/G]GAAGTTCAAGACCAG | 11060 |
rs527880398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902370 | TCCATCAGTGCAAAG[A/G]TAATTTAGGGAAAGG | 11060 |
rs527897519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908075 | GTGAAACCCGTCTCT[A/G]CCAAAAATTAAAAAA | 11060 |
rs527906305 | snp | A/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906319 | CCTTGTGATCTGCCC[A/G/T]CCTTGGCCTCCCACA | 11060 |
rs527912005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863364 | ATACAGAAAGGCTGG[A/G]CGTGATGGCTCATGC | 11060 |
rs527925129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69764062 | GATGGTCAGTATTGT[C/T]CCTATATCACATGAA | 11060 |
rs527928748 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940263 | AGTGTGCAAGGGAAG[G/T]TGTTGCATCCCCAGG | 11060 |
rs527950239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69820479 | GAAATCCTGATCTTA[A/G]GTGATCCACCCACCT | 11060 |
rs527956189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913836 | GCACTTTGGGAGGGC[A/G]AGGCAGGTGGATCAC | 11060 |
rs527997784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771262 | TAATTATTATTTTTC[C/T]TTTTGAGATGAAATC | 11060 |
rs528008665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779523 | TAGAATTTATCTGAT[A/T]GTTTTAGTTTTGCGG | 11060 |
rs528015216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907645 | ATGCAAATAACAGGA[A/G]TGTGGGGATAAGTGG | 11060 |
rs528022463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844956 | GCCCCCTTTCCACTT[C/T]GCTGTTGCAGGTATG | 11060 |
rs528051137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777670 | TATAGTTTCTACCCT[A/G]TTAGTTTGTATTTTA | 11060 |
rs528052980 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69769316 | AGCAAGACTCCATCT[C/G]AAAAAAAAAAAAAAA | 11060 |
rs528085110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906547 | ACAGTTAGCTCTGCT[A/G]TAACATATGTGCTCC | 11060 |
rs528104506 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856395 | TAACACCACTATAAA[C/T]ATTTGGTAAAACTTG | 11060 |
rs528141977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770205 | CTTTGGTTGGGGACT[C/G]CTGGATAGTCTCAGG | 11060 |
rs528157664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919356 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 11060 |
rs528162123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825311 | CACCTGTAGTCCCAG[C/G]TACTCAGGAGGCTGA | 11060 |
rs528175462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69911266 | ATAAGTATTGGACCT[A/G]GTAGCTCAGGGTGAA | 11060 |
rs528189960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867775 | TTTGTGGAGTTTGGC[C/T]TGACTGGCACTGCCA | 11060 |
rs528199224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874944 | GGAGGATCGTTTGAG[A/C]CTAGGAGGCAGATGT | 11060 |
rs528214414 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69878575 | TTTTGTTGCCCAGGC[C/T]GGTCTCCAACTCCTG | 11060 |
rs528218039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777172 | AATACACATATGGAT[A/G]TACACATATGTGTAT | 11060 |
rs528223378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847727 | TCTTTTTAATAACCC[A/G]TTCTTGCAGGTTCCC | 11060 |
rs528276414 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69798758 | GGCGGTGGATGGACT[C/G]CCCAGTGAGACCAAG | 11060 |
rs528300210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69841972 | TCAAATCTCAAACAC[A/G]AGTTGAGCTCCTCAA | 11060 |
rs528305730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933796 | GTCTGAGCCTGCCCT[G/T]TTCACTGACCAGCTG | 11060 |
rs528329811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69813143 | TTATTCCATGGGTTA[C/T]AACTTATTTCTGGTG | 11060 |
rs528360767 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69762444 | TGCCTGCACGGGGCG[A/G]GCCGGGGGCGGCGGG | 11060 |
rs528370250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900787 | CCTTGGCCTCCCAAA[A/G]TGCTGGAATTACAGG | 11060 |
rs528409484 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69830091 | CCCAAGTAGCTGGGA[-/T]TTACAGGCACATGCC | 11060 |
rs528430781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69901505 | GCAAGCTCTGCCTCC[C/T]GGGTTCATGCCATTC | 11060 |
rs528446470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852475 | AACTGGGTTTCACCA[C/T]GTTGGCCAGGTTGGT | 11060 |
rs528448051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804376 | TTATTTTTGTGCCCA[C/G]TACAAATAGGGATCT | 11060 |
rs528465570 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892032 | CTCCTCCACCATACT[C/G]TAGGTGCCATACGGG | 11060 |
rs528507559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938248 | TGAACTCCTGGGCTC[A/G]AGCAGTCCTTCCATC | 11060 |
rs528511606 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856289 | ATCCAATCTGAAGAT[A/G]TGGGGGCATTGGAGG | 11060 |
rs528527656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817876 | GTTGGGATTACAGGT[A/G]TGAGCCATTGTGCCC | 11060 |
rs528538451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69898114 | CTCACTGCAACCTCC[A/G]CCTCCTGAGTTCAAG | 11060 |
rs528541168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811269 | TTTCAAGGAGGTGAA[C/T]GTAGCTTGAAGTAGG | 11060 |
rs528550768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768574 | GAGATTGCATCACTG[C/T]CCTCTAGCCTGGGCA | 11060 |
rs528584007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851628 | TGCTTCCAAGTTTTG[A/G]CAATGATGAATAATA | 11060 |
rs528594043 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825430 | TTCCATCTCCAAAAA[A/C]AAAAAACCCCAAAAA | 11060 |
rs528598101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898764 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCAC | 11060 |
rs528620410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926333 | TGCGGGAACCAGCAT[A/G]TGTTGGGTTTCATTT | 11060 |
rs528621677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811847 | CTGTTAAAATTTGCT[A/G]CATTTGCTTTCACTG | 11060 |
rs528661967 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776605 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 11060 |
rs528667981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69791305 | TGATCTTGGTTCACT[A/G]CAACCTCTGCCTCCC | 11060 |
rs528670808 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69784738 | GTTGGGAAAAAGCAC[A/G/T]GTTGTTTGAATTGAG | 11060 |
rs528676793 | in-del | -/AAAT | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69916065 | AATCTTTGGTAACAA[-/AAAT]AAATAAAAATCACTA | 11060 |
rs528677348 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69880801 | ATGTTACGAGCTGAT[A/C]TTCAGTAGAAAGAAC | 11060 |
rs528682608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918571 | TAGCCTAAGCCTACT[A/G]TCTGACCCTTTGCTG | 11060 |
rs528710503 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838447 | ACCCTCCTTGACTTA[-/AA]AAAAAAAAAAAAAAA | 11060 |
rs528725209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69811394 | GGAGGTTTGCTTGAG[C/T]GTGGGAGTTCAAGAC | 11060 |
rs528734463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886373 | AAGTATCTAGGTATC[C/T]GGCCTAGATACTTTG | 11060 |
rs528743613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773626 | GCTGGGACTACAGGC[A/G]TGCACCACCATGTCT | 11060 |
rs528751956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925572 | TCTTCCTTCCCTGTT[C/T]CTGTCCCTCTGTTTT | 11060 |
rs528762262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69797940 | CCAGGCTGGTCTTGA[A/G]CTCCTGGGCTGAAGC | 11060 |
rs528778314 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941892 | ACCGAGGCAGCCCCC[A/G]ACTTCTGGGCTGGGC | 11060 |
rs528798681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886984 | TATGCAATCATATAT[A/G]TGGAAAATTCTCTGC | 11060 |
rs528851463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923608 | ATTTCCCAGGAGAAC[C/G]CTGAACGCTTTACAG | 11060 |
rs528853348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931367 | CCCGGAGCTGGCTGT[C/G]TCTAGGAAGCTAGTT | 11060 |
rs528864044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885574 | CAGTTCCATGTGTGC[C/T]AATTTTTACATGGTT | 11060 |
rs528871611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69789177 | GTTCTCCTGTCTCAG[C/T]CTTCCAAGTAGCTGG | 11060 |
rs528880034 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905821 | ATTCTTCCTTTCAGC[A/G]AAGCATGGTGAAACT | 11060 |
rs528895880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69830634 | GAGTGTGAGTGTTGG[A/G]GGGCCGCGGGGAGGT | 11060 |
rs528904794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69916368 | CCCCCAGCTAATTTT[C/T]AAAAAATATTTTTGT | 11060 |
rs528908748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69789581 | CTCCTCCTTGGAAAA[A/G]ACCAGTATTGTTTCT | 11060 |
rs528917905 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833750 | GAATATTTTCATTAT[A/C]TATGTTCCATTTAGT | 11060 |
rs528936686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891073 | CTCTGTGGGCTGACT[C/G]GGGGCCTGGAGATCG | 11060 |
rs528946005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795108 | AGGCGTGGTGTTGCG[C/T]ACTGGTAGTCCCAGC | 11060 |
rs528950684 | in-del | -/TGGA | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69887452 | AATTTTTTGCAAGGC[-/TGGA]TGGAGTGCAGTGGCA | 11060 |
rs528960165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802560 | TAATGTCCTCAAGGC[C/T]TATTCATGTTGTAAC | 11060 |
rs528970993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884558 | GCTTGAGCCTGGGAG[A/G]TCAAGGCTGCAGTGA | 11060 |
rs528981873 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813680 | ACCATGTTGCCCAAG[A/G]CTGGTCTTAAACTTT | 11060 |
rs528982583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844866 | TCATTCTGCACTCAC[A/G]TGGAACCTGTTGCCA | 11060 |
rs528993889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69930935 | TATCCTGTTTATTCC[A/G]AATGACACTAGAGTT | 11060 |
rs529016844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775805 | GTTTAAAAAAGAAAG[C/G]TGGACATGATGTATT | 11060 |
rs529064578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904830 | TGAGCAAGAATGCCC[A/G]GGAGAGAAAACATCC | 11060 |
rs529133515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767716 | TGAGGGCTGTTTGTG[A/T]TTAATCATTTCTCAG | 11060 |
rs529154421 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761165 | AAGTTATTGGGCAGG[C/T]ACAGTGGCATTCGCC | 11060 |
rs529155607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872454 | ATCTCCTGACCTTGT[G/T]ATCGCCCGTCTTGGC | 11060 |
rs529173043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775241 | CCTTGGGGTATAAGG[A/C]GGGCATCTCTCAAAG | 11060 |
rs529175769 | snp | A/G | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933281 | TTTAGCTCAAGCCCA[A/G]AAGGACTCTGAATTC | 11060 |
rs529192657 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69831506 | GCCCTATTTATCTAT[A/G]TTTATTAGTACCACA | 11060 |
rs529237083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909902 | ACTAGTCGGCACACT[A/G]TGATGGCCTGTGGAC | 11060 |
rs529238341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863564 | GAATTGCTTGAACCT[C/G]GTGGGGGCAGAGGTT | 11060 |
rs529246620 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930826 | GCAGTGAGCCATGAT[C/T]ACACCACTGCACTGC | 11060 |
rs529266555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773217 | TGACTCTCATGCTGT[C/T]GCTCAGGCTGGAGTG | 11060 |
rs529284379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815362 | ACTCAGGCTAGGGTA[C/G]AGTGGCTCGAGCATA | 11060 |
rs529312655 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | WWP2 | GRCh38.p7 | 16:69908834 | ACCACCACCTGGGAG[C/T]GGCCCCTTCCTCCAG | 11060 |
rs529318652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764939 | TCAGACATGGTGGCT[C/T]ATGCCTATAATTCCA | 11060 |
rs529329878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922308 | CCCTTCCCAGACCTT[G/T]CTTACCCTCAGCTGT | 11060 |
rs529335784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864234 | TGAGCTGGACATGGT[A/G]GTGCGCACCTGTGAT | 11060 |
rs529337047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829025 | TCCTGTTCCCGTATT[C/T]TGTATTTCATCATAT | 11060 |
rs529374959 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781400 | ACCCAGGCTGGAGTG[C/T]GGTGGCACAATCTTG | 11060 |
rs529399253 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929064 | ATCAGCTGTGAGGGA[C/T]TTGGGTGGGGGGCCT | 11060 |
rs529410474 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69877586 | CTTGGCTAACTGTCA[C/G/T]AAGAGTCCCAGCTTT | 11060 |
rs529420805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858422 | GCTCTTCATTCGCCA[A/C]AACTTCTGGGTGGGT | 11060 |
rs529421072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850255 | AGCCGGGCGTGGTGG[C/T]GTGCGCCTGTAGTCC | 11060 |
rs529435430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935601 | CCGGACGTGGGTTCC[C/T]GCACCAGCTGGCTCT | 11060 |
rs529476349 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864933 | ACTTTGTCAATCCTG[A/G]TAGATATGTAATGAT | 11060 |
rs529482022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850736 | TTGACATGTAAGATA[A/T]TAGGGATGATAGCGT | 11060 |
rs529485039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810090 | AAGGACCTGATGGGC[A/G]ATGGTTGCCCTAACT | 11060 |
rs529486811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801712 | CCACTATACCTGACT[A/G]CTGTTAACATTTTGA | 11060 |
rs529487746 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | WWP2 | GRCh38.p7 | 16:69848638 | CTAGATGCTGTTGCT[-/A]AAAAAAAAAAAAAAA | 11060 |
rs529505849 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897159 | CCAGGCTGGAGTGCA[A/C/G]TGGCGTGGTCTCAGC | 11060 |
rs529506117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839663 | AAAAAACAACATCAT[A/G]TTTTAACACAAATAA | 11060 |
rs529509304 | in-del | -/G/GG | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923320 | GTGTGTTGGGGGGGT[-/G/GG]GGGGGGGGTGCGTTC | 11060 |
rs529521856 | snp | C/G | 1.65089e-05 | 0.00287301 | intron-variant | WWP2 | GRCh38.p7 | 16:69936270 | TCCAGGAAAGACCCT[C/G]ACACGGTAGACATCT | 11060 |
rs529529806 | in-del | -/CAA | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69874674 | TTGAGACTTGTATGG[-/CAA]GATGATTTACTTGCT | 11060 |
rs529544939 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP2 | GRCh38.p7 | 16:69813906 | TAGGTAAAATTTACT[A/G]TGTGATAAAGATGGC | 11060 |
rs529547250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815989 | CAATTTTAAACTTAA[A/T]TTGGATAAATTACTC | 11060 |
rs529555035 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834063 | TGTACCTCAGCCCTT[C/T]TCCTGTAGCCAGACT | 11060 |
rs529566277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941379 | CAGATTCTCGACCTT[C/T]CCCCGGCCCGGGAGG | 11060 |
rs529582860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903426 | TGAACATAAAAGATG[A/T]CAAAAGTGGAGACTG | 11060 |
rs529586831 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802216 | ACAGGCATGAGCCAC[C/T]GTGCCTGGCCTATAT | 11060 |
rs529619366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807652 | AAAAAAAAGAAAAGA[A/T]AAAGGAAAATGAAAG | 11060 |
rs529652086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809255 | ATGACAATGGCGTAC[A/G]TAGCCTATGTACCTA | 11060 |
rs529675467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934522 | TTTACTGAACATTAA[A/G]TATGTGCTCTGTTGA | 11060 |
rs529678575 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896558 | AATGATATCACATTC[C/T]CAGTGGCCCTTAAAA | 11060 |
rs529710232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907510 | ATTCAGTGTAAAACA[G/T]AAAGGCCCACAGCAC | 11060 |
rs529712418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69901570 | GGCATGTACCACCAC[A/G]CCCAGCTAATTTTTT | 11060 |
rs529727451 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940604 | ACAGCAAACTCCCTC[A/C]GACTTTGTCCATGTA | 11060 |
rs529739947 | snp | C/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941464 | ACAGCGCAGCCTCTT[C/G]TGTCCCTTTCAGTCA | 11060 |
rs529771355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902145 | ATTGAGCATTAATTT[C/T]CTGAAGACCTTTGGG | 11060 |
rs529777489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807072 | TATCTCTTTTTGCCC[A/G]GGATGGAGTGCAATG | 11060 |
rs529796178 | snp | A/G | 1.67083e-05 | 0.00289031 | intron-variant | WWP2 | GRCh38.p7 | 16:69929444 | CTTTCTTCTCATGTG[A/G]CAGAGAAGAGACAGG | 11060 |
rs529804609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939540 | GGCCCTGGGGTGTTG[G/T]GTTGGAGAGATGGGG | 11060 |
rs529823837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69855334 | GTATTTTTTAGTTCA[C/T]TTCAGTCTGCCCTCT | 11060 |
rs529848055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786688 | ACTCCTGACCTCAGG[A/T]GATCTGGCCATCTCG | 11060 |
rs529857886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843591 | CCCAAACGAGGCCAG[A/G]CACAGTGGCTCATGC | 11060 |
rs529887646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794253 | CTATAGGCTGGGTGT[A/G]GTGGCTCATGCCTGT | 11060 |
rs529921127 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925784 | TTTTGGTCTTGAGTT[C/T]CAAGGTGTCTACTCA | 11060 |
rs529926138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69787646 | CCTGTTCATGCCCTA[C/G]GGCTCGTTGCTACCT | 11060 |
rs529932219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928847 | AAGCAAGAAAGAGGC[A/G]TGCCAGGGTATGAGA | 11060 |
rs529938035 | in-del | -/TGAGGGCGATGAGGACTAGGATGATGGCGGGCAGGATAGTT | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69807596 | CCACTCCTGCCTGGG[lengthTooLong]TGACAGAGCAAGACC | 11060 |
rs529943483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843080 | TGGATAAAAGGAACT[G/T]TTGAACAGGAAACTT | 11060 |
rs529947228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793578 | AGAGGTGTGGAAAAT[C/G]GTCCTGTGCTGAGTC | 11060 |
rs529987693 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870042 | CATCTTCTGACCTAA[C/G]AGCCTAGGCTCTTGA | 11060 |
rs529998867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849601 | AAATATGGAATAGGA[C/T]TGAGACAGTGGTCAA | 11060 |
rs530002367 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873030 | GGGATGTAGATGTTT[C/T]GCTTGGATGAATTGT | 11060 |
rs530009447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841938 | CTCTAACACACAGAC[G/T]GAGTTCTGTTCCTGG | 11060 |
rs530019426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889735 | GTTTTCACTGCCTCT[C/T]CTGGTTATCAGTTTG | 11060 |
rs530023292 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | WWP2 | GRCh38.p7 | 16:69840159 | CCCTGAACCTGCAGA[C/T]GGAGAACAAAGGCAG | 11060 |
rs530055421 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848622 | AGCCTGGGCAACAGA[A/G]CTAGATGCTGTTGCT | 11060 |
rs530064778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845446 | GAATGATGGGCTTCT[C/G]CCTGCTGTCTCCCAG | 11060 |
rs530087910 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69765819 | ATGAAGTGAGACTCC[G/T]TCTTGCTTTTGGAGA | 11060 |
rs530095887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893835 | AGGAGTGAGCCACTG[C/T]ACCCAGCCCTCAGAA | 11060 |
rs530109492 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842240 | ATTTCCAGAGATCTT[G/T]TAACTGACTCAGTAG | 11060 |
rs530134061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847697 | ACAGCTGTGAGCCAC[C/T]GCGCCTGGCCAGGCT | 11060 |
rs530183412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778766 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11060 |
rs530216603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933313 | TGCCTGAGGCTCGCA[C/T]CCAGGGCACGGGTGT | 11060 |
rs530304893 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69824693 | GTATATATTTGAAAA[A/G]ATTCATAGATTACAA | 11060 |
rs530314938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920264 | TCTTAGTAAGTTGCT[C/T]CAGGGTCGACGATCA | 11060 |
rs530322671 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796414 | GACACTTCGATATCC[C/T]GCAGCTAGGCAAGAT | 11060 |
rs530323907 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69913723 | AGAAAACAGGAGCTT[C/T]TAGAAATTAATATAT | 11060 |
rs530339497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69785810 | TTGTTGTTTTTTAGT[A/G]TAGATGGGGTTTCAT | 11060 |
rs530341084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777850 | GGTGGGAGGATTGCC[C/T]GAGCTCAAGAGTTCC | 11060 |
rs530344763 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937346 | GTAAAACTCCCACTT[C/T]GGCAGGGCAGATGGG | 11060 |
rs530346641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875749 | TCACATATTCAGGCC[C/T]ACTTCTTATTCTAGC | 11060 |
rs530371114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913062 | GAATTTTTGCTCTCG[C/T]TGCCCAGGCTGGAGT | 11060 |
rs530402445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912105 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 11060 |
rs530408058 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807643 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAAAAGGAA | 11060 |
rs530409045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874131 | AGGGATTTCTGCCCA[C/T]TCCAGTGCTGAGGGC | 11060 |
rs530410118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834819 | AGACGTGAGCCATGG[C/T]GCCCAGCCTGCACTT | 11060 |
rs530411742 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69867135 | GCCACTACACCTGGC[C/G]AAGGCTTTTTTTTTT | 11060 |
rs530448149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827216 | ATCTTTGTTTCATAA[A/T]CTTACTGCTCAAACA | 11060 |
rs530451618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850108 | AGATGAAAAGTCGGC[C/T]GGGCGCAGTGGCTCA | 11060 |
rs530470350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784360 | CCGCCTTGGCCTCCC[A/G]GAGCGCTGGGAATAC | 11060 |
rs530473069 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867696 | TGAGTGAGGACACAC[A/C/T]GCATCCTGAGAAGGG | 11060 |
rs530473410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860149 | AAGACCCCCATCGCT[A/T]TAAAAAAAAATCAAA | 11060 |
rs530478153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776628 | TGAGGTCAGGTGTTC[A/G]AGACCAGCCTTAACA | 11060 |
rs530503241 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760421 | GCCACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 11060 |
rs530512922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832395 | TTTTAGTGTATTTCT[C/G]TAAAAGATAAGAACT | 11060 |
rs530518146 | in-del | -/A | 0.336245 | 0.234652 | intron-variant | WWP2 | GRCh38.p7 | 16:69922078 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 11060 |
rs530526771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905584 | TCTGCAGATATTCCA[A/G]AATCTGAAAACAAAA | 11060 |
rs530550012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833004 | GACCGCAGGTGCACG[C/T]CACCACGTCCAACTA | 11060 |
rs530569165 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800957 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG | 11060 |
rs530582415 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762025 | CCTACTAAAGGAGCT[C/T]AATTAAGTATTTGCT | 11060 |
rs530592558 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69853503 | TTCTCATTGGTGCAA[A/C]CTAAATCACACCCAG | 11060 |
rs530613522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900670 | TGGGACTACAGGTGC[A/G]TGCCACCATGTCTGC | 11060 |
rs530617503 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812547 | GCAGTGGTGTGAACA[C/T]GGCTCACTGCAGCCT | 11060 |
rs530637014 | snp | A/T | 0.000861512 | 0.0207368 | intron-variant | WWP2 | GRCh38.p7 | 16:69783796 | ACAACAACAACAACA[A/T]CAACAACAAAATATT | 11060 |
rs530654376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854034 | ACAGAGAGAAACATC[A/G]TATTCCTGACAGTGA | 11060 |
rs530658941 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69824198 | TGCCGGAATAGCCAT[A/G]TTAACATCAGACCTC | 11060 |
rs530691477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769247 | GCTTGAACCCGGGAG[G/T]TGGAGGTTTGCAGTG | 11060 |
rs530703006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813067 | CAAAGAAGGGCTTTC[C/T]GTTTTCATGTATGCG | 11060 |
rs530703534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938512 | TAATCCCAGCTACTC[A/G]GGAAGCTGATGCATG | 11060 |
rs530719936 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781998 | TTAAGATTAAATTTT[C/T]GGAGCCGGGCGAGGT | 11060 |
rs530733641 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69762374 | AGGAGTTCGGCGCCG[A/C]TTCTGTGGCCACGGC | 11060 |
rs530759295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932882 | GAGAGCGCTGTGGCC[C/T]GCAGCGACCTCTCCG | 11060 |
rs530782386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850936 | GAGTGGTACATTTGT[C/T]AGAATGATGAGCCTG | 11060 |
rs530789269 | in-del | -/AAAAAAA/AAAAAAAA | 0.0726307 | 0.176182 | intron-variant | WWP2 | GRCh38.p7 | 16:69846049 | GCCAGACTCCATCTC[-/AAAAAAA/AAAAAAAA]AAAAAAAAAAAAAAA | 11060 |
rs530796279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906229 | AGGTGCCTGCCACCA[C/T]GCCCAGCTATTTTTT | 11060 |
rs530799086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811196 | TCCTCTTGTAGCTCC[C/T]CACTCCTGCAGCTCT | 11060 |
rs530811492 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803166 | CCTGTTTCTTTTTGG[C/T]TGAATTATTTTTATT | 11060 |
rs530859118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906427 | AATGCAGTCCACTAA[C/G]CAGACATCCCAGTTT | 11060 |
rs530866408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899973 | GTCAATATTTATCTA[C/T]AATGTTATTTTTAAG | 11060 |
rs530867489 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69816600 | GTATTTTTCTGATTA[A/T]TATTATTTCATGCCT | 11060 |
rs530867959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823389 | CTAGAGGTTGAGTCC[C/G]TGGAGAAAGACTGGG | 11060 |
rs530870830 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810585 | GGCACCCACCACCAC[A/G]CCTGGCTAATTTTTT | 11060 |
rs530896505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859416 | AGAAATTAGCTAGGC[A/C]TGGTGGCGCATGCCT | 11060 |
rs530959430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69810468 | TTTCGCTCTGTCCCC[C/T]AGGGACATGAGGGCA | 11060 |
rs530968313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851572 | GTTTATCCATTCACT[C/T]TTACATTCCTCCTCC | 11060 |
rs530972274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932056 | GTGAACCCGCCAGGC[A/G]CGGTGGCTCACGCCT | 11060 |
rs530973832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69924999 | TTTTTTCCCCTCCTG[C/T]GTGTGGTTCTTGGAG | 11060 |
rs530976393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839427 | TCTAGCCTGCCTAGG[A/G]CTTGGTGCTTCTGCC | 11060 |
rs530980882 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782538 | GTAAGAGGAGATGGA[G/T]AATTGCTATGGGATT | 11060 |
rs530989021 | in-del | -/AA | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837373 | CCCAGCCCATTGGCT[-/AA]CTTTTTGAAGACAAA | 11060 |
rs531008239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879486 | TTAACGTGTCCTTTT[A/G]TGTCTGGCTTATTTC | 11060 |
rs531012129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797377 | TGGAATCAGACCGGC[C/T]GGGTGCACAGTCTGG | 11060 |
rs531012762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831698 | GTGAGAGTTATTCCC[C/G]AAACAGCTTGACTGA | 11060 |
rs531014586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69840024 | TGGAGAAAGCATTCC[C/G]AGAGAAGCCAGCAAA | 11060 |
rs531034136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866051 | AGGTGTCTCTGACCT[C/T]GCATCTCATCATGGC | 11060 |
rs531034253 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69858531 | CCTTTATCACAGCCG[C/G]CTTGTGCTTGCAAGG | 11060 |
rs531099197 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903553 | GAGGGTGGATCACAA[C/G]GTCAGAAGATCGAGA | 11060 |
rs531104051 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923690 | AAATGCGTCTTCTTT[C/T]AATGTCTTAAAATAA | 11060 |
rs531120418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804083 | TTTGGTATTGAAAGA[A/G]CTCTTTATTTGTTAA | 11060 |
rs531122895 | in-del | -/AAAT | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761120 | CTGTCTCAAGCAAGC[-/AAAT]AAATAAATAAATAAA | 11060 |
rs531127016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789978 | CTGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 11060 |
rs531141241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892212 | CTTTTAATTATACTT[C/T]AAGTTCTGGGGTATA | 11060 |
rs531158133 | snp | A/G | 0.00072612 | 0.0190403 | intron-variant | WWP2 | GRCh38.p7 | 16:69925531 | CCTTCCGTCAGCCAC[A/G]GTGCTCTGTCCTCTC | 11060 |
rs531165565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69790434 | TCATTTTCATGTTGA[A/G]TAGCTGAGGAGGAGG | 11060 |
rs531213759 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763755 | AGGTTTCATATTTTA[C/T]TTGGCTGCTAGCCTA | 11060 |
rs531230368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922636 | AAGAGGAGGGGCAGC[C/T]GGTTGGCTCATTGGA | 11060 |
rs531263989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885769 | AAGTGTTAAGTGGGG[A/T]TATCAATTGTAACTA | 11060 |
rs531276163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890021 | GTGCAGTAGTACAGT[A/C]TTGGCTCACTGCAGC | 11060 |
rs531281098 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69800662 | CTCCGCCTCCCAGGT[A/T]CAAGCGATCCTACCA | 11060 |
rs531289756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69844301 | GAGGAAACAATTTCT[C/T]AAGCTAGAACAGCGG | 11060 |
rs531309319 | in-del | -/GTGTCGCTACTACTTT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773100 | TCTGGGAAGACGCTA[-/GTGTCGCTACTACTTT]GTTTCCTTAGCAACA | 11060 |
rs531334559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795042 | AGTTCGAGATCAGCC[A/T]GGCCAATGGGGTGAA | 11060 |
rs531338295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890561 | GGGAACAATGCAGAA[C/T]CATGTTGGCAGAAAG | 11060 |
rs531356238 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930880 | CCGTCTCTAGAAAAC[A/C/G]AACAAACAAATAAAT | 11060 |
rs531356831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782143 | CAGAAATTAGCTGGG[C/T]GTGTTAGCGGGTGCC | 11060 |
rs531358985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774477 | GTTCAGGCTGGTCTC[A/G]AACTCCTGGATTCAA | 11060 |
rs531386390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69890100 | GCTGGGACTACAGGC[A/G]TGCACCACCATGCCT | 11060 |
rs531405778 | in-del | -/CTGCAGTGAGCTGGACCGTGCCACTGCT | 0.0197687 | 0.0974348 | intron-variant | WWP2 | GRCh38.p7 | 16:69938556 | CCTGGGAGGTGGAGA[-/CTGCAGTGAGCTGGACCGTGCCACTGCT]CTGCAGTGAGCTGGA | 11060 |
rs531408729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809160 | GGGTTGGGTAGCAGG[C/G]AAATCAGATCAGAGT | 11060 |
rs531433458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935566 | GAGCCAGCCGGCCAG[C/T]GTGCGGGGCAGATGC | 11060 |
rs531446301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69791900 | TTCTAAAGGCTTTTT[C/T]GTTGCCTTTCTTGAA | 11060 |
rs531471189 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69767273 | ACATGTATTGAATGC[A/G]TGTTGTTTGTCAGGC | 11060 |
rs531486636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915531 | TCCAGTTTGGGCAAC[A/G]TAGTGAGATCCTGTC | 11060 |
rs531499382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69830037 | TTGGGTCATTGCAGC[A/G]TTCGCCTCCTGGATT | 11060 |
rs531517528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781592 | GAGCACAAGGTGATC[C/T]GCCCGCCTCAGCCTC | 11060 |
rs531523198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789003 | GAGTATTTTTGAAAT[A/G]CAAATGTTATTTATA | 11060 |
rs531550847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822823 | TAATTTAGAATTTGC[C/T]ACTAGCCATATTAAA | 11060 |
rs531576651 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867199 | GTTTAATTACTCCAC[A/G]TGATCTGTTGCAAAG | 11060 |
rs531578376 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833138 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCT | 11060 |
rs531620111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923503 | TCAGGGAGACTGTCA[C/G]TAAAGACCTTTTTGG | 11060 |
rs531628228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69821024 | GAGCCCAGTTCCAGC[C/T]GCCAAATGCAAGCCG | 11060 |
rs531631346 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838184 | AATGACAGCTTATTA[A/G]GAACTCGGTAGGTGC | 11060 |
rs531631363 | snp | A/G | 6.68103e-05 | 0.00577933 | intron-variant | WWP2 | GRCh38.p7 | 16:69936469 | TGAGTCTCAGGCGCC[A/G]GGGGCTCCGCTCCAG | 11060 |
rs531638953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862691 | CTTGGAACCTGGTAT[C/G]CAGCCAGCCATGAAT | 11060 |
rs531651905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69772399 | TACTGATGCAGGGCA[C/T]GTGAGCCCCAAAACT | 11060 |
rs531663240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830583 | GACCAAGCCAGAGTT[C/T]TCATTACATTCTGGG | 11060 |
rs531678970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916196 | TGGAAGTGTTGTTGT[G/T]GTTGTTGTTGTTGTT | 11060 |
rs531702189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920966 | CTGCCTCTCTTAGCA[A/G]CATTATTCTGGGTTT | 11060 |
rs531721319 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760368 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 11060 |
rs531781252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857190 | CTCATTGCAACCTCT[A/G]CCTCTGGGGTTCAAG | 11060 |
rs531792449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765599 | GAGGCTGAGACGGGC[G/T]GATCACTTGAGGTCA | 11060 |
rs531837345 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908376 | TACAAATTTTTGTCC[C/T]AAGTGCATTTTGAAG | 11060 |
rs531844965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849777 | CGTGCCACTGCACTC[C/T]AGCCTGGACAACATA | 11060 |
rs531877419 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839036 | CTCTAGAAAGTGCTG[A/G]AATTTACCTTAGTGT | 11060 |
rs531879007 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69789935 | CTGTTGACTGAAAGC[-/CT]TGCCAATAACAGAAA | 11060 |
rs531890622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863467 | AACATGGTGAAACCC[C/T]GTCTTTACTAAAAAC | 11060 |
rs531898483 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842609 | TCTGCATTGATTTGC[C/T]TAGGATAATGGCCTC | 11060 |
rs531937550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903230 | GTCCTCTGAAGACCT[C/G]CTGAAACTGTTGAAT | 11060 |
rs531990836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69821503 | TTCCCTTCCCCTGGT[C/T]CAGGCTGCTGCCTCC | 11060 |
rs532000768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814417 | TTCCTAACCTTCCTC[C/T]ACTCTCATGAGAACC | 11060 |
rs532013552 | in-del | -/TTTA | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69882324 | TTCAAATATCTTTCT[-/TTTA]TTTTTTAGTTTTTAA | 11060 |
rs532016812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939505 | CAGCTTCATAGCCTC[A/G]AGTCTGGCAGCTTTT | 11060 |
rs532021484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908137 | GTAGTCCCAGCTACT[C/T]GGGAGGTTGAGGTGG | 11060 |
rs532036747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819556 | GAGGCCTTCTTTGAT[A/G]ATACTGTCTTCATTT | 11060 |
rs532083311 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921932 | TACAAAAATTAGCTG[A/G]GCGTGGTGGCGGGCA | 11060 |
rs532088643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815238 | AAACTCCTGATCTCA[A/G]GTGATCAGGCCATCT | 11060 |
rs532120348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806340 | ATATTTTATATTGGG[G/T]TTTTCCATCTATATT | 11060 |
rs532139778 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69934336 | GGCTCACCCTCTCGG[A/G]GCTCCACCCTTTGCC | 11060 |
rs532149900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907077 | ATTTTCTCTTGAGAA[G/T]ACCTGAAGTTTGCTT | 11060 |
rs532151848 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899017 | CCAATCTGCAGGATT[A/C]TTAATAATGCTAGGT | 11060 |
rs532188306 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776776 | GAGGTTGTGGTGAGC[C/T]GAGATTGTGCCATTG | 11060 |
rs532188780 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895521 | TGTAATCTAGCACTT[C/T]GGGAGGCCGAGTCAG | 11060 |
rs532193252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842949 | GTTGGGATTACAGCC[A/T]TAAGCCACTGTATCT | 11060 |
rs532228377 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69803542 | GAAGGTCCATTCATT[C/G]GTTGTTCTATCTCTG | 11060 |
rs532272068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933849 | CTTGTCACAGGGCTC[A/G]ACTCCCTGGGACACG | 11060 |
rs532273932 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940028 | CCCGCAGCCCTTGGG[A/G]GGCCCCCGTGGATGT | 11060 |
rs532289232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849087 | TCCGGTGAGCTCTAA[A/G]TAGATCATCAACTGT | 11060 |
rs532295117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927902 | CCTGGGCTCGAGCGA[C/T]CCTCCTGCCTCAGCC | 11060 |
rs532300763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848298 | TCTTCTAAAAATACA[A/G]AGTTAGCCAGGCGTG | 11060 |
rs532304458 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830438 | AGAGAAAAAGTTTGT[A/T]AACTGGCTTTGTAAA | 11060 |
rs532331070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882342 | ATTTTTTAGTTTTTA[A/G]TTTTTTTTATTTCTT | 11060 |
rs532331157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799672 | CCCTAAAACAGAACA[A/T]AGGAGCTGTGTGTAT | 11060 |
rs532342194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69929350 | TGACAACAGGGAGAT[A/G]AACTCAGACCCAGCA | 11060 |
rs532344384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793007 | TAAACCGAATCTAAT[C/T]ATGAGGAAACAATTG | 11060 |
rs532369782 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832290 | TAGCCATCTATGACG[A/G]GCCATTCCTGTCTCA | 11060 |
rs532376981 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69786042 | ATTTGGCCAGAGACC[C/G]TCCTTGAGGTGTTTG | 11060 |
rs532381544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69922581 | CCTTTTCTGCTCCAC[A/G]TAACACCTTGACATC | 11060 |
rs532383032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793475 | AGATCAGTCTTCCTG[A/G]AGGCTCAGAGATTAG | 11060 |
rs532403415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791433 | GGGTTTCACCGTATT[A/G]GTCAGGCTGGTCTCA | 11060 |
rs532413899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894438 | TATGTGGTTACACAC[A/G]TCTGCACGTTTTAAG | 11060 |
rs532417858 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894892 | GGCAGCCAGCACGCC[A/G]CTGTGGTTTCTTACA | 11060 |
rs532422197 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | WWP2 | GRCh38.p7 | 16:69861693 | GGGAGGAAGAATTGA[-/G]GGGGGGTGCAGGTGG | 11060 |
rs532453579 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761939 | CCATTCTGTATTTGG[A/G]ACATACATATTACAC | 11060 |
rs532476231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894910 | GTGGTTTCTTACATA[A/T]CGGAGGGCGTTGTGT | 11060 |
rs532482467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888447 | TCAGTCGCCTGGGGC[A/G]GAATCAATGCTACCT | 11060 |
rs532493228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853384 | ATTTGAAGTGGGTGT[A/G]CAGGCGATGAGGCAT | 11060 |
rs532500239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932790 | CTTGCCTTCACCCTG[A/G]TCCACCCATAAAAGT | 11060 |
rs532504672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847032 | CCAAGTAGCTGGGAC[A/T]ACAGGTGTGTGCCAG | 11060 |
rs532506726 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69805185 | GCTGGGATTACAGGC[A/G]CCCAACACCATGCCT | 11060 |
rs532539091 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941749 | CAGCTGTGGGTGGTG[G/T]TGTTGTGGATGTTTA | 11060 |
rs532558085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841080 | ACTCATTCAACACAT[A/G]TATATGTAATTGTAT | 11060 |
rs532581274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875048 | AATTACAGCAAAAGT[A/C]TATATCTCATAAGTT | 11060 |
rs532608597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804497 | GCTTATATTAAAAAC[A/G]TATGTGTATTTGGGC | 11060 |
rs532621472 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896131 | CTGCACTTTCTTTCC[-/T]TTTTTTTGGAGACAG | 11060 |
rs532627747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887734 | GTTATGTTGATCTTT[A/C]CTGCTACTCTTTTGT | 11060 |
rs532639450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777734 | ATAAGTTCAGAGGAA[A/G]TATGTTGTTTGTATT | 11060 |
rs532645053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846491 | TTGGGGAGGTCGAGG[C/T]GGATGGATCACTTGA | 11060 |
rs532653184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938405 | GGCAGATCACTTGAG[A/G]TCAGGAGTTCAAGAC | 11060 |
rs532675420 | snp | C/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940355 | TGGCTGTTCGGGACT[C/G]AGAGCGCCAAGGGTC | 11060 |
rs532685948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792132 | GTGGGGTGTGACTGC[A/G]CGGTTTCCAGTTCCC | 11060 |
rs532718180 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69881534 | GTTAATAGTAGTATA[A/C]TAATTATTATTTTAG | 11060 |
rs532728171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833880 | GCCCTGCGGGGCCTG[A/G]CTGATGTGCTCGGTG | 11060 |
rs532730333 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796595 | TTACTGAATGCATAT[C/T]GCTTTCGCACCCCTG | 11060 |
rs532733804 | snp | A/G | 3.40721e-05 | 0.00412734 | intron-variant | WWP2 | GRCh38.p7 | 16:69799147 | ATGATCTGCTTGGAT[A/G]TAATGAATCAGGTAT | 11060 |
rs532800673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69868333 | TGTTTCTGAAAGTAT[C/T]CTCTCTCCATGCTGA | 11060 |
rs532803173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880840 | TTATTGGTGCTGGCT[G/T]TCTACGTGCCTGAGT | 11060 |
rs532804378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872978 | TTAGAGACTGCTGGT[C/T]GTTTGGTAGTTTGTC | 11060 |
rs532806439 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838270 | GCAGGTAGGGAGACT[C/G]ATGCTCAGGTTAGGT | 11060 |
rs532812177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832225 | ATGTGAAACATACAC[A/G]GAGGTGGAAAAACAG | 11060 |
rs532834600 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798042 | GTCTTTACACCATGC[A/G]TTTTTAACCCATGGA | 11060 |
rs532835057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833239 | TTAACTTAGAGGTAG[C/T]CCTCCCTCTTTTTAC | 11060 |
rs532863831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874334 | TGTGAATGAGGACAT[A/C]TTCATCCCTCGGGCT | 11060 |
rs532871374 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799774 | TGCCCTGTGCTTACT[C/T]GGCACTCAGTAAACA | 11060 |
rs532891828 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836072 | CCTCCCAAAGTGCTG[A/G]GATTACAGACGTGAG | 11060 |
rs532896690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783068 | CAGGCTGGGGTGCAG[C/T]GGCGTGATCTCAGCT | 11060 |
rs532912300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917147 | AAATAAGGAAGGGAA[C/T]GTATTGGCTCATGTA | 11060 |
rs532933031 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932810 | CCCATAAAAGTTAAC[A/C]GGCCCTCTGGGAAAT | 11060 |
rs532980903 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69787311 | ATGGTGATTTCAGGC[C/G]AGGTGCAGTGGCTCA | 11060 |
rs532985191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906165 | GCAAGCTCCGCCTTC[C/T]GGGTTCACGCCATTC | 11060 |
rs532993215 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760635 | GGCGTGAGCCTCCAC[A/G]CCCCACCAGCCAATT | 11060 |
rs533035089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924598 | GAGGGGGTGTGGGGG[A/G]GATTCTAATGTAAAC | 11060 |
rs533040352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824130 | CATTCGGGCGGCTTC[C/T]GCCTGACCGTCCATT | 11060 |
rs533061297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867078 | TGACCTCAGGTGATC[A/C]ACCTGCCTCAGCCTC | 11060 |
rs533079118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789880 | AGTAAAAAAATCCAC[A/G]TGTAACTTTTGACTC | 11060 |
rs533132324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811918 | GTTTCTTTCATCCCT[A/G]AATACTGATGTGTCT | 11060 |
rs533142176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816492 | TTATATATGTAATAT[A/G]TAAACATATATACAC | 11060 |
rs533193297 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941879 | ATGTGTGTCATGGAC[C/T]GAGGCAGCCCCCGAC | 11060 |
rs533200284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937772 | CCTTGCCTCCCACAC[C/G]TTGCAAAAGGAGACG | 11060 |
rs533209605 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882238 | TGGGATTATAGGTGT[C/G]AACCACTGCGCCCAG | 11060 |
rs533215664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822266 | GCATTTTCTTAGGAT[C/T]ATGAGCCTTGCTTGT | 11060 |
rs533218885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817311 | TGGAGTGCAGTGGTG[C/T]GATGTTGGCTCACTG | 11060 |
rs533229042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916111 | TATGAGAAAGCTAGG[A/G]AGGTTCCAGATTTTT | 11060 |
rs533244295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908907 | ACCATGAGTCACCCA[A/G]TGGCTTCTTGAAACG | 11060 |
rs533270074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69864318 | AGTGAGCCATGATCA[C/T]GCCATTGCACTCCAG | 11060 |
rs533298758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822711 | TTGAGGCAGGAACAA[A/G]CTGGTTGCTGTCAAG | 11060 |
rs533299013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69816102 | AGAAACTGCTAACCC[A/G]GTCCTGCATACCCAG | 11060 |
rs533314667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936786 | TGTGCCTAGACCCAC[C/T]GTCTCACGTGTGCCC | 11060 |
rs533315722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817915 | TTCTTGTAAAGATAC[C/G]TTTATGCTCCTCTTT | 11060 |
rs533318506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851417 | CATTTCCAGAATGTC[A/G]TATAGCTGGATCATA | 11060 |
rs533324035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765855 | GGAGTTGGGGGCGGG[G/T]GTTCTCACTTTTGCC | 11060 |
rs533324089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775035 | ATCATATAAATTTAC[A/G]TGACTAAGACCTGGA | 11060 |
rs533325736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69865327 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCACA | 11060 |
rs533328483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69931067 | TTAAATTAACATAGC[A/G]CCAGCTTTCCTTAGG | 11060 |
rs533359282 | in-del | -/TA | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69874673 | ATTGAGACTTGTATG[-/TA]GGATGATTTACTTGC | 11060 |
rs533362436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903990 | GCAGCTAAATTCTTC[A/G]GGAGTGCTGGAGAGT | 11060 |
rs533369945 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838403 | GCCAGAGACTTAGGT[A/G]CTGGATCTTGGCGTA | 11060 |
rs533380051 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885278 | TATAGCTGTGCATAA[A/G]GTGAATTGCCATCTG | 11060 |
rs533394916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858525 | GGGCGCCCTTTATCA[C/T]AGCCGCCTTGTGCTT | 11060 |
rs533402723 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857547 | TTGACTGGCTCCCGG[C/T]CTGAAGGTTTTCTGT | 11060 |
rs533442338 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903874 | GCAGCCCACCCAAAT[A/G]TTAGAGTTTTCCAAA | 11060 |
rs533458137 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69780333 | ATATTTCAGGTACTA[-/T]TATAGCATTCCATTT | 11060 |
rs533484785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774370 | AAGCGATCCTCCCAC[C/T]TCACCTCAGCCTCCC | 11060 |
rs533508377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920488 | GCCATTTTCTTGGGT[G/T]GTTGTGGCTGCAAAA | 11060 |
rs533527174 | snp | A/G | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69835373 | TTAGTCCCATTATGT[A/G]TTATAGGGTTCCTCT | 11060 |
rs533538158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793741 | GGGAGCAATTGGGGA[A/G]GTCACAAATCTTGTG | 11060 |
rs533547703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786249 | TCCCGGGTTCAAGCA[A/G]TTCTCTGCCTCACCC | 11060 |
rs533566422 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848500 | TCAATAGCTAGGTGC[A/G]GTGGCTCATGCCTGT | 11060 |
rs533567787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69921394 | CTTGCTGGGCTTCAA[C/T]TGAGACCTTGTTCTT | 11060 |
rs533598040 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806580 | CTTTTTTTTTCAGTT[A/T]TCCCCCCCATAATTA | 11060 |
rs533599681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931411 | CACATGCTATTGCCT[C/T]CTGGCCCAGCAGGCT | 11060 |
rs533599754 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69789288 | AGGCTGGAGTGCAGT[A/G]GTGCGATCTCGACTC | 11060 |
rs533599874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69796527 | GCTGCCCAGTAGTAC[C/T]GCATATGACTATTCT | 11060 |
rs533648346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793165 | AGACCAGCCTCGCCA[A/T]GATGGTGAAATCCTG | 11060 |
rs533651306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928284 | TGTTTTCAGGAGAGA[A/C]GCAGATTTGAAGGCT | 11060 |
rs533686790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69802631 | TTTGAGACAGGGTCT[C/T]GCACTGTCGCTCAGG | 11060 |
rs533687655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882477 | AAGCATTACGGACAA[C/T]GTAAAGCATATAAGA | 11060 |
rs533692275 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820939 | TTTGCAGCCAGTGTC[C/T]GGCTCACCTCGGAGG | 11060 |
rs533693300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897856 | GAGGTTACAGTGAGC[C/T]GAGATCGTACCACTG | 11060 |
rs533704915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891163 | GCTTTTGGTTGGCTG[A/T]TGGAAGCCAGAGAGA | 11060 |
rs533722323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843246 | TAATGTTGGTTAAGA[C/T]CTCCTACGCTTAGAG | 11060 |
rs533734267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69892369 | CCCCTGACAGGCCCC[A/G]GTGTGTGGTGTTCCC | 11060 |
rs533745966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928944 | GGTGCAGAGCACTGA[G/T]CAGAGAGGTGCGAGG | 11060 |
rs533760680 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69816752 | GTATACATATACACA[C/T]GTATACATATACACA | 11060 |
rs533762808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902708 | ATAACCTCTGACAGG[A/G]ATGCGCTGATGAAAA | 11060 |
rs533789032 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69856663 | CCTGTAGTCTCAGCT[A/G]CTCGGGAGGCTGAGG | 11060 |
rs533792005 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69836079 | AAGTGCTGGGATTAC[A/C]GACGTGAGCCACCGT | 11060 |
rs533815610 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69786736 | AATTACAGACGTGAG[C/T]GACCATGCCTGGCAG | 11060 |
rs533822457 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69869139 | GTGATCCACCTGCCT[A/C]AGCCTCCCAAAGTGC | 11060 |
rs533849569 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764268 | GCAGTGGCACAATCA[C/T]GGCTCACTGTAACCT | 11060 |
rs533864550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842627 | GGATAATGGCCTCCA[C/G]TCTCCGGCTATATTC | 11060 |
rs533871945 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911184 | CCGATTCACTTAATC[A/G]TGGCCGTCCCTGCAT | 11060 |
rs533883565 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935110 | GGATTGAGAAGCGGA[C/G]CCCGTGGGAGGCACA | 11060 |
rs533887714 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890621 | GAGCTGTTTGTTTTC[C/T]TTCCGCTGAGCGAAT | 11060 |
rs533887801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934611 | GGGAGGTGACACTGT[C/T]ACGGCATTTGGGAAT | 11060 |
rs533916872 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69877973 | CCACCGTGCCCAGCT[A/C]ATTTTTGTATTTTTA | 11060 |
rs533925333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889320 | ATGAAGCGAGACCCC[C/T]GTCTCAAAAATAAAA | 11060 |
rs533953012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906744 | GATTAGCTGGGCCTC[A/G]TGGCATGCACTTGTT | 11060 |
rs533971080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772724 | GGTGGGTGTGTCTTG[G/T]GGGGAGGTGCTTTTG | 11060 |
rs533980075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861604 | CATTTTAACTCTAAT[C/T]GTGCCTTTCCCGGTT | 11060 |
rs533982560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874579 | AAACAAGAGTGAATG[A/G]CAGCCCGTCTGTATA | 11060 |
rs533990449 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69797757 | AGCCAGGCACGGTGG[C/T]GGGCGCCTGTAATCC | 11060 |
rs534074306 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69863375 | CTGGGCGTGATGGCT[C/T]ATGCCTGTAATCCTT | 11060 |
rs534084854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763359 | GATCATGATTTTGAG[A/G]TTGAATACTTGTGTT | 11060 |
rs534109183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798934 | TGGCACCTCCGACTT[C/T]TTCTACCTATGGTAC | 11060 |
rs534130685 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761981 | TGAAATTCAAATTTA[A/G]GTGGGTGTCCTGTAC | 11060 |
rs534137529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69840977 | AATCTCAGTGGCCGG[A/G]TGGGCCTTGACTGTG | 11060 |
rs534165400 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933690 | TGGATATTGTGATGT[A/G]AAGTCTTGGAACACA | 11060 |
rs534167954 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934597 | TGCTGCCTGTCTCTG[A/G]GAGGTGACACTGTCA | 11060 |
rs534185309 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813348 | TATATTTTTAGTGGA[C/G]ATGGGGTTTCTCCAT | 11060 |
rs534198604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69901020 | AAGGGTCCTTCGGGG[A/G]AGGACTGAGTTTAAC | 11060 |
rs534203261 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814429 | CTCCACTCTCATGAG[A/G]ACCCTGGCACTCAAC | 11060 |
rs534209341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819797 | AAACATTACTGAGTC[A/G]TGCAGTCATTGCCAT | 11060 |
rs534238015 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897558 | CTGCTATACGGTGTT[C/G]TGTTACATGAACAGA | 11060 |
rs534277194 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69860593 | ATCAGCAAAGGGTCT[C/G]ACTCTCCCTTGGTAG | 11060 |
rs534278761 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761370 | TTGAAGTCAGGTGTT[C/T]GAGACCAGACTGGTC | 11060 |
rs534287673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825959 | TTTTACTATGGAAAA[A/T]TTCAAACATAAATAA | 11060 |
rs534289251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69911724 | ACATGTGGCTTGAAC[A/G]TGTGTTTATTTCTAT | 11060 |
rs534325864 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69819113 | TGCATTGCCTTTAGG[A/G]TATATTCTGGGATCC | 11060 |
rs534342648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853634 | TGAGACCAGACTCAG[A/G]GACTGACGAAGAGGA | 11060 |
rs534344613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846613 | GTAATCCCTGCTATT[C/T]GGGAGGCTGAGGTAG | 11060 |
rs534361473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938592 | CACTGCTCTGCAGTG[A/G]GCTGGACCGTGCCAC | 11060 |
rs534368292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939724 | GGCCTGACTGGCAGC[C/T]CCTGAGCCCTAGCCA | 11060 |
rs534387553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69807179 | TAGCTGGGGTTACAG[A/G]CACACGTCACCATGC | 11060 |
rs534423069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848710 | TCCTTTCTTATGTGT[A/G]TATGTATTTAAGCTA | 11060 |
rs534466005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812126 | TATTTATGTCTTTCA[C/T]GACATTGGCATCGGC | 11060 |
rs534484773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907166 | GGGCTATCTGAAATC[A/C]GATGGGAGTTGTAAC | 11060 |
rs534498928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854624 | GGCACGATCTTGGCT[C/T]ACTGCAAACTCTGCC | 11060 |
rs534499735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791745 | GGCTGGTTTCAAACT[C/T]CTGGACTCAAGCAGT | 11060 |
rs534510994 | snp | C/T | 0.00113951 | 0.0238423 | intron-variant | WWP2 | GRCh38.p7 | 16:69939306 | TGGGAAGGGACGTCT[C/T]TGCTGACGTCGGCGT | 11060 |
rs534512661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862105 | ACTTTCGCTCTTGTT[G/T]CCCCGGCTGGAGTGC | 11060 |
rs534553364 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864621 | GTGGCACAATTTTGG[-/C]TCACTGCCACCTTGG | 11060 |
rs534555937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69813880 | TATTTTTGTCCCAAC[A/G]TAATCCAATATAGGT | 11060 |
rs534583277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804629 | TTCTCTTTTTTTTCA[A/C]AGTCTTCATGCTTCT | 11060 |
rs534595744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847208 | TCCTGTCTCATCCTC[C/T]AGAGTAGCTGGGACT | 11060 |
rs534612816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900048 | TCTCCATTTGGGGGT[A/G]TTTAGGTTGCTTCCA | 11060 |
rs534614774 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830606 | TTCTGGGTTCTGGGT[-/A]AAGACCCTGCCAGAG | 11060 |
rs534617718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932901 | GCGACCTCTCCGCTC[A/G]AGACCTCTCCCGGTG | 11060 |
rs534656233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932337 | CTCCATCTCAAAAAC[A/C]AAACAAACAAAAAAA | 11060 |
rs534661943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845738 | TTTCTTAGTGGGATC[A/T]TGCCTCTTCTTCAAG | 11060 |
rs534667063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923929 | ACACACAGACACACG[A/C]CCCCATGACTTGGAA | 11060 |
rs534675845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69796905 | AAAATCTGAAGGTGA[A/G]TTTGGCCTTTGCCAA | 11060 |
rs534707191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69831022 | CTGCTTACTCTCACC[C/T]GCTTTTGATGGGCCT | 11060 |
rs534720047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839496 | ACAGGACTGAATCTG[C/T]CTGGTATCCTTGGGG | 11060 |
rs534725899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925071 | TGAGCCGGAGCTGAG[A/C]GGAGGCACTGGGCCG | 11060 |
rs534727374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768934 | GGACAGAGGAAGGAG[G/T]CCAAGAAAGAAGCAT | 11060 |
rs534734874 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760600 | CACCTGCCTCTGCCT[C/T]CCAAAGTGCTGGGAT | 11060 |
rs534783271 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773084 | AAGGGAAGAACTGGC[A/C]TCTGGGAAGACGCTA | 11060 |
rs534813242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936835 | TCAGGCCTCTTGCTT[C/T]AGTCTTTATCTCCAC | 11060 |
rs534834489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891809 | TTACCCATCCCATCC[A/G]GGCTAGAACCTGGTC | 11060 |
rs534845052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69919028 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTTGCC | 11060 |
rs534845099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927160 | AGGAAGAACATTCTG[G/T]CTAAAGGCCAGGGCT | 11060 |
rs534863962 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899406 | TTTATTCTGATATGC[A/G]TGTTATTTCACATTT | 11060 |
rs534868956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805315 | TGCTGGGATTACAGA[C/T]GTGAGTCACTGCGCC | 11060 |
rs534879308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893505 | TGTCATTCACTGGCT[G/T]GACTGGCTTTGGGTT | 11060 |
rs534903357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69840650 | TGGTTGGGAAGGGTA[C/T]GCTGTGTTCTTCTAG | 11060 |
rs534949218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867229 | GGTGACAATGGTCAG[C/T]GAGGCTGCACTGAGG | 11060 |
rs534986163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831940 | CACAAGCGATTATTC[C/T]GCCTCAGCCCCCCAA | 11060 |
rs534990716 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838603 | GGTTAGGCTCTGCTG[C/G]GGCTGGAGCAGCTGC | 11060 |
rs534997582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789381 | ACTACAGGCGTGTGC[C/T]ACCGCGCCTGGCTAC | 11060 |
rs535006874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878991 | CAGCCTTGTAAATAT[C/T]GGTTTATAATTTTTT | 11060 |
rs535015404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783290 | GCTGGGATTACAGGC[A/G]TGAGCCACTACGCCT | 11060 |
rs535018586 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770447 | GGTTCTTGGAGGATG[A/G]CACCCTCAGAGAGGG | 11060 |
rs535072185 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893573 | TTTGTTTGTTTGTTT[-/TT]GTTTTTGTTTTTGTT | 11060 |
rs535079839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69781702 | ACTGGATAATAGAAA[C/T]GGGATAATTTATAAA | 11060 |
rs535108475 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907198 | CCAGATGTTGACGGT[A/G]TAGCCTATTAATACA | 11060 |
rs535108684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845030 | AGGAGTCTATTGGAT[A/G]AAGGTGTAGGGCTTT | 11060 |
rs535130156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877373 | CTTCATAGAATTGAA[G/T]AGGGTTCGGGTCTTG | 11060 |
rs535145109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885067 | CTTTAGAAACTCCCC[C/T]TACACACACACACCA | 11060 |
rs535145994 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69786581 | TCAGCCTCCAGAGTT[G/T]CTGGGATTACAGGCA | 11060 |
rs535177402 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837683 | CTCCATTTATGAAAC[A/G]ATGACCTTTGAGGTA | 11060 |
rs535190264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69915138 | CACCTGTCCCGTCTG[A/G]GAATCTGGGGATGCA | 11060 |
rs535192498 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69877893 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 11060 |
rs535206844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69873230 | TGGAAGAAATTGATT[C/T]GGGTTCCTTTGCAAT | 11060 |
rs535227393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776064 | ACTGGAGCCCTGTTG[G/T]TGTGACAGCAAAGTA | 11060 |
rs535245511 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890169 | TTGCCATGTTGCCCA[G/T]GCTGGCTTAAGCCAC | 11060 |
rs535257581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766834 | TCTTGGCTCACTGCA[A/C]CCTTCACCTCCCAGG | 11060 |
rs535263419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859772 | TCTCCCTGTGATTTG[A/G]ATCTCTCTGATTTTC | 11060 |
rs535264656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768371 | CCCAGCACTTTAGGA[A/G]GCCGAGGTGGGTAGA | 11060 |
rs535264988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776692 | CATTAGCTGGGCGTG[C/G]TGGTGCATGCCTGTA | 11060 |
rs535271303 | snp | G/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941926 | TGAGTCCTGGCCCAG[G/T]GGTCACCGGCTTCAG | 11060 |
rs535293837 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780256 | AGGCTGCCACTTGCC[-/T]TTTTTTTTTTTTTCC | 11060 |
rs535296484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782418 | GGCTCAGGTGGGGCA[A/G]GAGGAGGATGAGGCA | 11060 |
rs535349218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69903682 | CTGAGGCAGGGGAAT[C/T]GGTTGAACCCAGGAG | 11060 |
rs535370899 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890651 | TGCCTGGAAGGCCGG[C/T]CTCACTCCTGTGTCA | 11060 |
rs535371645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909284 | ACAGAAAGTTCTTTC[C/T]ACATGTGTCTCCTGG | 11060 |
rs535407639 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761361 | GCGGATCATTTGAAG[G/T]CAGGTGTTCGAGACC | 11060 |
rs535410114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816676 | ATTTTTCTGAATTCC[C/T]TCATATGTATATACA | 11060 |
rs535411075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69871210 | GATCACTTGAGCCCA[A/G]GAGTTTGAGGCTGCA | 11060 |
rs535423563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69904992 | CCAAATTAGGAGTAT[A/G]TGTTTTTTGTAACAA | 11060 |
rs535424016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856447 | GGTAAATTTTACTCT[A/G]TGTAAATTATACCTT | 11060 |
rs535455580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908974 | TTATTCCGGGTCACT[C/T]GATTGCTTTTCCTAT | 11060 |
rs535481914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849328 | TCCACTGAGGTGACT[A/C]AAGGCTGCTTGATTG | 11060 |
rs535541619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922737 | CTTCCTTCTGGCTTT[A/T]TTTTTCAAGTTGTAC | 11060 |
rs535543570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829347 | ACCTCAGTTAAAAAA[C/T]CCTTTAGCACTGTGC | 11060 |
rs535570668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814025 | GCACAAGCATCTCCA[A/G]GAAATATGTCAGACA | 11060 |
rs535578777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821905 | GAAACAGGGTCTTAC[C/T]CTGTCACCCTGGCTA | 11060 |
rs535608626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858810 | TAAGAATAGGTAATA[C/T]CTCATTTATACTAGG | 11060 |
rs535608900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850457 | TAGTAGGAGACAGAT[A/G]CATGGATGAGTTAGA | 11060 |
rs535610453 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863712 | AAGTTCCCCAGTGCC[C/T]CTTTGTAGCCAGCTC | 11060 |
rs535618226 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941979 | TACCCTTTCGGCACC[C/T]TCTGCCTCCGCCTGC | 11060 |
rs535668256 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811359 | ACCTGTAATCCCAGC[-/A]ATTTTGGGAGGCTAA | 11060 |
rs535675912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851064 | TCCACTGGCTGGAGT[C/G]CAGTGGCTCAATCTC | 11060 |
rs535730718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816301 | TAAAAATAATTACTT[A/C]GCCCAGTGCAGTGGC | 11060 |
rs535735525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849900 | GGTACCTTATTATAC[A/C]TTTATTTATTGCATA | 11060 |
rs535739775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889474 | TGGGTTTGAATCCCC[C/G]CACCATGTGACCTTG | 11060 |
rs535749315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857967 | AGTACAACTCTATAA[C/T]GACAAAATGACACAA | 11060 |
rs535802426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764202 | ACAATAGAAAATTTT[A/G]TTTTTATTTTATTTT | 11060 |
rs535815542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933917 | CACAGCTCCTGTGCA[A/G]ATGTGCACGAAGGGA | 11060 |
rs535815778 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69927298 | AAGTGAGAGTGATCG[G/T]CAGCTTGCTAACCCA | 11060 |
rs535843267 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847403 | TATTTATTTTTCTTA[-/T]TTTTTTTTTTTTTTA | 11060 |
rs535861159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902979 | GATCAGGGAGGACCC[A/G]CAGGGACATTTAATC | 11060 |
rs535877130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928056 | TTCAGTCGAGTCATA[C/G]ATACCAGGTAAGGCA | 11060 |
rs535878842 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790361 | AAAATCATAAGGAGG[-/A]AAAAAATTTTACTAT | 11060 |
rs535883094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834319 | TGGGCTTGCTTTTTC[C/T]TCTGCCTAGAATGTT | 11060 |
rs535886334 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940761 | TTCCCAAACAGCCAC[A/G]CCTCTCAGGAACCCA | 11060 |
rs535931757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821081 | GCAGTTACATCAGCG[A/G]CTACTGTTTTTTTGA | 11060 |
rs535939452 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69901820 | GCCAGGCGTGGTGGC[A/G]AGTCCCTGTAATCCC | 11060 |
rs535941345 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901875 | AGCATCACTTGAACT[C/T]GGGAGATGGAGGTTA | 11060 |
rs535943855 | in-del | -/GA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809809 | AGAGAGAGAGAGAGA[-/GA]TAGGAAGGAAGGAAG | 11060 |
rs535946511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862784 | GAGTGTAGTGGTGTG[A/C]GTGTGATCACAGCTC | 11060 |
rs535971367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814555 | GATTTTGAAAAGCTC[C/T]GTACTTTATGCTGTC | 11060 |
rs535977893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847922 | TAGCAGGGAGTCAAG[C/T]TGGAATGAAGCCCAC | 11060 |
rs536002340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798914 | TGGGAGGTACAGATT[C/G]CCTGTGGCACCTCCG | 11060 |
rs536025848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794693 | ATTAGAAAAATGTAG[A/C]ATTTGCTGCATTCTT | 11060 |
rs536039809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69869183 | ATGAGCCACTGTGTG[C/T]GGCCAACAGCTTTTG | 11060 |
rs536040638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828347 | TGTCTTTCTTGCAAG[G/T]TCATCATCTATTATT | 11060 |
rs536053749 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839514 | GGTATCCTTGGGGAC[A/G]GGGTGCTCTGGGCCA | 11060 |
rs536058369 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837016 | GCAGCCTCGACCTCC[C/T]GGGCTCAGGTGATTC | 11060 |
rs536062793 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798036 | GCTGTTGTCTTTACA[C/G]CATGCGTTTTTAACC | 11060 |
rs536084469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69921958 | GGGCACCTTTAGTCC[C/T]AGCTACTTGGGAGGC | 11060 |
rs536088631 | snp | C/T | 3.30611e-05 | 0.00406565 | intron-variant | WWP2 | GRCh38.p7 | 16:69930113 | AGCCCTTCACCCTTT[C/T]CTTCCCGTGTTTCCA | 11060 |
rs536094333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771435 | TATTTTTAGTAGAGA[C/T]GGGGTTTCCCCATGT | 11060 |
rs536118289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896002 | GGCTTCCTCATCACC[A/G]TCTCAGAACTTAAAC | 11060 |
rs536132579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858208 | CTTCCGAGGAGTTAT[G/T]TCTTCCACCTGGTTT | 11060 |
rs536151459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920414 | AATTGGATGGAATCT[A/G]GTCTTTCACCACATT | 11060 |
rs536173543 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69890099 | AGCTGGGACTACAGG[C/T]GTGCACCACCATGCC | 11060 |
rs536192264 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834206 | TCTGGCTACCTCCTG[C/T]CCTCATCTGCTCCTC | 11060 |
rs536197198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69800811 | CTCAGGTGATCTGCC[C/T]GCCTCATCCTCCCAA | 11060 |
rs536202981 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823262 | TGAGATATTTTACAT[A/G]CTTTTTGGCCTCAGG | 11060 |
rs536208062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910859 | GTTGAGGTGGGACAC[C/T]ACTAATCAAGCTGTC | 11060 |
rs536218517 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69848384 | GAATCTGGGAAGTGG[A/C]GGTTGTGGTGAGCCC | 11060 |
rs536231378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874449 | AGATTTATTTAGCAG[C/G]CTTTTTTGGCTGCGC | 11060 |
rs536236683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888604 | TCTCTTGAATTTTAT[C/T]GTATCAGCCCACGGA | 11060 |
rs536251619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825832 | GGATCTCCCTATGTT[A/G]CCCAGGCTGGTCTCA | 11060 |
rs536283117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777324 | CTTTTTTTTTGAAAC[A/G]GAGTCTCATTCTGTC | 11060 |
rs536290324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867846 | GTCCCCTCCCCCTAA[A/G]TGGTGAGGGGGCTTG | 11060 |
rs536299795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880556 | TTTACCTTCCCATCA[A/G]TCAGGTAACACAGTA | 11060 |
rs536312907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790934 | TCCTATGGATTGCCT[A/G]TTCATGTTCTTTGCC | 11060 |
rs536358768 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69784027 | TCCTCAGACATTGGG[A/G]GGTCTCCCAGACTCT | 11060 |
rs536362523 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894936 | TGTGTTTGGACTGCC[A/G]ACTTACTTCAGCTCT | 11060 |
rs536363108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880899 | CACGAGTCTGTGATA[C/T]ACCACACGCACCTAA | 11060 |
rs536404729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921087 | CTCAGGCTCGCTGGG[A/G]ATGTGGGAGGGTTCT | 11060 |
rs536405859 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762221 | AGACGATAAAAAGGC[C/G]TCCTCGAGGCCAGAG | 11060 |
rs536408695 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826396 | CATAGTGAAACTCTG[-/T]CTCTACTAAAAATAC | 11060 |
rs536461062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69813232 | CAATGGCGCGATCTT[C/T]GCTCACCGCAACCTC | 11060 |
rs536465360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805566 | TTCTGACTGGGAATC[C/T]TTTTGATTTATTAAT | 11060 |
rs536471613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914110 | AAAAAAGAAAGTGAT[A/G]AATTTGGAGATAAGA | 11060 |
rs536472503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907363 | CATTATGCTCACATC[A/G]TCCGCTTCTATATCA | 11060 |
rs536474804 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69913887 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCCGTC | 11060 |
rs536509822 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940812 | AGGCAGGCCTGACCC[A/G]GCGGCACAGCCTGGC | 11060 |
rs536511982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793115 | AATCCGAGCACTTTG[A/G]GAGGCCTAGGTGGGA | 11060 |
rs536522988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785548 | ATACAAGTAAAAGAT[C/G]CATTCAAAGTACAAG | 11060 |
rs536609915 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818300 | GCAACCTCTGCCTCC[A/C]GGGTTCAAGCAATTC | 11060 |
rs536612188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69824834 | GCAGTACAGTGGTGT[A/G]ATCTTGGCTCACTGC | 11060 |
rs536634323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859665 | CATCAGCGGGGGTCC[C/T]TCTCAACTCCTTAAG | 11060 |
rs536652483 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69818324 | GCAATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 11060 |
rs536665944 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788871 | GAAAGAATATTGCTT[C/T]GGGTTCCATAGCTCT | 11060 |
rs536671723 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69820351 | GGTTCAAGTGATTCT[C/T]CTGCCTCCGCCTCCT | 11060 |
rs536672426 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807981 | ACAAAACAAAAAACA[G/T]TCTTAGTGTTACAAC | 11060 |
rs536681988 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938181 | ACAATTAACTATTAA[-/T]TTTTTTTTTTTCAAT | 11060 |
rs536708900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865856 | AGAACCACACCATAG[G/T]CAGTGGCCTCTTATC | 11060 |
rs536719110 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861646 | TACCCGCCCTCTCCT[-/T]TTTTTTTTTTTTTTC | 11060 |
rs536722543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69841117 | ATGCACTAGGTCTTA[A/G]ACCAGGCCCTAGCCA | 11060 |
rs536722602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832925 | AGTGATGCAAACATG[A/G]CTCAGTGCAGCCTTG | 11060 |
rs536740179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823712 | ACCTCAAGTGATCTG[C/T]CTGCCCCAGCCTCCC | 11060 |
rs536757564 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69796149 | GCTATTGGTTATGTT[-/A]AAAAATGTGTTTGTT | 11060 |
rs536760413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69776010 | AAACTCCTTCTTAAA[C/T]AGAGTGTATGCCTTT | 11060 |
rs536768121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873613 | AGCAAAGTGATGGCC[A/G]TGAGCCATAGTATAG | 11060 |
rs536771913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866389 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 11060 |
rs536776345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817427 | CTAATTTTTGTATTT[G/T]TAGTAGAGACAGGGT | 11060 |
rs536818228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69846548 | CAACATGGCGAAACT[A/T]CTTCTCTACTAAAAA | 11060 |
rs536826938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69861467 | CGGAAGTCTTTCTGT[A/G]ATTTAGAATGGACTT | 11060 |
rs536841640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886590 | CATGGTGAAACCCCG[C/T]CTCTATTAAAAATAC | 11060 |
rs536876372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847335 | GGCGATCCACGCACC[G/T]TGGCCTCCCAAAGTG | 11060 |
rs536903576 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924954 | TGGGCAGGGCTTGTG[A/G]GAATGATTTCATTGG | 11060 |
rs536904583 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933834 | AGGTTAGCCCGGGTG[A/C]TTGTCACAGGGCTCG | 11060 |
rs536917405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69898956 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs536924471 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761340 | CACTTTGGGAGGCCA[A/C]GGTGGGCGGATCATT | 11060 |
rs536955809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852773 | TTCTCCCAGTCTGCG[A/G]CTTGTCTTCTCATTC | 11060 |
rs536979360 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790997 | GTCTTGAAATATTTT[-/A]ATTATATTTCTTGGA | 11060 |
rs537057422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811498 | TGGCTTATACCTCCC[A/C]ACACTTTGGGAGGCT | 11060 |
rs537058114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898350 | TCTTAAAGATTTGTA[C/T]AGCAACTGGAATTTC | 11060 |
rs537063474 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69778222 | AGAAATTTCAATAGA[A/T]CTACCAGACTTAGTA | 11060 |
rs537100432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809502 | CCAGGTACGGTGGCT[C/T]ACGCCTGTAATCCCA | 11060 |
rs537103236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69801137 | GAGGTTCCAGTGAGC[C/T]GAGATTGCGCCACTG | 11060 |
rs537124483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910047 | ATTGCAGCAGACTCT[A/G]TGGCTTGCAAAACCT | 11060 |
rs537144008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816847 | CATTTATTCTTCCTC[C/T]GTACATTCAAGGTAG | 11060 |
rs537166424 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918187 | GTCCATTTTCCCTGA[C/G]TTGCACCCTGACTTG | 11060 |
rs537169089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810777 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 11060 |
rs537175373 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69868940 | TTGTCCAGGCTGGAG[-/T]GCAGTGGTACAATCT | 11060 |
rs537227145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69790179 | CTCAACCCGGGAGGC[C/T]GAGGTTGCTGTGAGC | 11060 |
rs537237134 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913249 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGACA | 11060 |
rs537242054 | in-del | -/A | 0.0704125 | 0.17392 | intron-variant | WWP2 | GRCh38.p7 | 16:69858117 | ACCTTTAGAACCAGT[-/A]AAAAAAAAAAAGTTT | 11060 |
rs537267723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917198 | ATCCTGATTCCAAGC[A/G]AAGCTTGGGCTACTC | 11060 |
rs537268715 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69915412 | GATAGCAAATATGGC[-/A]AAAAATCAAGAAATA | 11060 |
rs537282615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840482 | TTTGTAAATATGTAA[C/T]TGTTTGGTTTGATAG | 11060 |
rs537283033 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904800 | AATCCCCAGGAGTCT[A/C]ATCAGTCAGAGCCTT | 11060 |
rs537283243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69925872 | TTCAGATCTGTGACC[A/G]TATGGTTGGAATGAT | 11060 |
rs537294818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812024 | CTAATTCAGATTTCC[C/G]AGCTGTCACAGTCCA | 11060 |
rs537375150 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780002 | TTTTGCCATATTTGC[C/T]CCAGAACTTTTTTCT | 11060 |
rs537383354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804542 | TCCATTGAATCCATC[A/G]TTTTATTAGCCTTTC | 11060 |
rs537425632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844612 | CCTCGTTTGTTGTCA[C/T]TGGTGTTGAGAATGA | 11060 |
rs537439958 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861278 | TTGAAGTTTGGGAGG[A/G]CATTTGAGCACTCTT | 11060 |
rs537449639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891260 | GTTTAGGAGATCCAG[A/G]CAAGGCGGGTTATTA | 11060 |
rs537468711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915062 | GGTGTGAGATGGACA[C/T]ACAACTGTCCCCGTC | 11060 |
rs537495503 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940783 | AGGAACCCACCTGGC[A/G]GTTCCGTGAGCTCAG | 11060 |
rs537514953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764846 | TTATGTTATAGTAAA[C/T]GATCATATAATGTAT | 11060 |
rs537572622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890910 | CATCTTTTCCTTGGG[G/T]CATTTAGAACGTGAT | 11060 |
rs537584141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883592 | ACTTTAAGTTCCGGG[A/G]TACGTGTACAGGATG | 11060 |
rs537591805 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69802161 | TCTCGATCTCCTGAC[C/G]TCGTGATCTGCCCGC | 11060 |
rs537628040 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941116 | GACATGAAAACCAGC[A/C]GAAAGGCCCTGAGCT | 11060 |
rs537668054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783170 | GCGTGCCACCATGCC[C/T]GGCTAATTCTTGTAT | 11060 |
rs537677668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775418 | TAAGGTATCTTAAAC[A/C]CCATCAGCCATGTCC | 11060 |
rs537683492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766033 | AGCCTAGGCCTGTCT[C/T]GAGACTTCTAGATCT | 11060 |
rs537696241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850080 | CAGGCTCTGAGCTGT[C/T]GTGGTGATTAAAAGA | 11060 |
rs537703248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788751 | CCTTCAATAGAGTGT[A/G]AGATCCACAGTAAGA | 11060 |
rs537732756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908466 | ATGCTGAATTTTTTT[A/T]AAAAATCCATGGAAT | 11060 |
rs537749554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923861 | ACTACAAAACAGAGT[C/T]GGAGGAACTTGGATT | 11060 |
rs537754129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789299 | CAGTGGTGCGATCTC[A/G]ACTCACTGTAACCTC | 11060 |
rs537798445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69762882 | GTTACCCGAGACTTT[A/G]ATGACGGTCCCATTC | 11060 |
rs537809528 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836984 | GTTGGAGTGCCCTGG[C/G]ATGATCTTGGCTCAC | 11060 |
rs537827835 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928014 | TTTACTGAGGTATGA[C/T]TGACAAATAATGTCT | 11060 |
rs537853974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829244 | AGCCTCCTGTCTGCT[C/T]TGCCTGTTTCTGTCC | 11060 |
rs537869554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901773 | TTTTGGTGTATCAAT[C/T]TATAAGGGCCACTTG | 11060 |
rs537893126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763458 | GCAGTGTAACTGGAA[C/T]GAATGTTCAAACTGG | 11060 |
rs537897919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855718 | GGCTGTTGGAAAGGC[C/T]TTAAGTTAGGAATGT | 11060 |
rs537905629 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | WWP2 | GRCh38.p7 | 16:69868665 | CATACACATGTGCAC[A/G]CACACACACACACAC | 11060 |
rs537917781 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69903192 | TGATCAAAGATGGAA[A/G]GGTGGGCCTTATCTG | 11060 |
rs537919090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69836137 | ATTGAACCTAAAAAC[A/G]TTAACAATAATTTCA | 11060 |
rs537973729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869154 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 11060 |
rs537982826 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788140 | GGCCAAGGCAGGAGG[A/C]TCACCTGAGCCCAGG | 11060 |
rs537996368 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69919002 | GTGCCCACCACCACA[-/C]CCGGCTAATTTTTGT | 11060 |
rs538012025 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814158 | TACCAAATGTGGGGT[C/T]GTTTGTTTGTTTGTT | 11060 |
rs538018398 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69847148 | GGAGTGCAGTGCCAC[A/G]ATCTCGGCTCACTAT | 11060 |
rs538026570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864519 | GCATCCTAATCCAGA[C/T]TTATTACTGTAAGTT | 11060 |
rs538052641 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69903612 | TCTCTACTAAAATAC[A/C]AAAAAATTAGCCAGG | 11060 |
rs538092827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929082 | GGGTGGGGGGCCTGG[C/T]GGGTTAGGGACTGCC | 11060 |
rs538104236 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819985 | TGGCTCATGCCTGTG[A/G]TCTCAGTGCATTAAG | 11060 |
rs538134570 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69821884 | TTTTGTTTTTTTTTT[A/T]AATAAGAAACAGGGT | 11060 |
rs538137692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69894694 | GGCAATGGGAAGCGA[A/G]GCTGCTTTGGTCTGC | 11060 |
rs538157284 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773699 | GTTGCCTAGACTGGT[A/C]TCGAATTCCTGGGCT | 11060 |
rs538205173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799440 | TTTGGAGTTTTGGGA[A/G]GGCTGAGGGCTCCTC | 11060 |
rs538211739 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860435 | ACACATAGCAGTGCC[A/G]TAAAGGGAACAATTA | 11060 |
rs538216534 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69847277 | TTTAGTAGAGACGGG[G/T]TTTCACCATATTGGT | 11060 |
rs538222410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939207 | AGTCTCTTCCTGGAA[A/G]CACGTCAGTGGGATG | 11060 |
rs538241152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798323 | TTAACATATACCTAT[C/T]ATGGGCTTGTATTGC | 11060 |
rs538245676 | in-del | -/T | 0.134119 | 0.221521 | intron-variant | WWP2 | GRCh38.p7 | 16:69904378 | CCAGTGCGCATTTTC[-/T]TTTTTTTTTTTTTTG | 11060 |
rs538266712 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69904439 | AGAGGTGTGATCACG[G/T]CTCACTGCAGCCTCC | 11060 |
rs538283778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933425 | GTTGCATAGCTGGTG[A/G]GCATGAGGTTTCTCA | 11060 |
rs538289851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841374 | GCTGAGACTTGGAGG[A/G]TGAGGAGTTTAGACA | 11060 |
rs538299085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876014 | GGCTGGCATGCAGTG[A/G]CATGATCTCAGCTCA | 11060 |
rs538331948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827461 | GCTTTATAATCACTA[A/G]TCCAAATCTTAATTG | 11060 |
rs538333564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900107 | TAACAGATGCACTTA[G/T]AGCTAAATTTTTGAC | 11060 |
rs538334171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820003 | TCAGTGCATTAAGAG[A/G]CTGAGGCGGGGGCAG | 11060 |
rs538334196 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69913349 | AAAAAAAGTTTTTTT[A/T]AAATTAGCTGAGTGT | 11060 |
rs538336660 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881862 | ACACCCAGCTATTTT[C/T]TTCTATTTTTAGTAG | 11060 |
rs538357561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938617 | TGCCACTGCACTCCA[G/T]CCTGGGCGACAGAGC | 11060 |
rs538369312 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69813460 | AGCCACTGCGCCCAG[C/G]CTTTTTTTTGTTGTT | 11060 |
rs538419251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69799958 | ATTCAGAGCAGTACC[A/G]TATGTGGCGAATGAA | 11060 |
rs538460348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69826678 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 11060 |
rs538482804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778394 | TCACTCAGAGTTTTG[G/T]AGTGATTAGGATGCA | 11060 |
rs538496161 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796407 | TGCTCAGGACACTTC[A/G]ATATCCCGCAGCTAG | 11060 |
rs538514760 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837011 | TCACTGCAGCCTCGA[C/T]CTCCCGGGCTCAGGT | 11060 |
rs538537779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856333 | AAAGGGGCACAAGGA[A/C]ATTTTGGGAGCAATG | 11060 |
rs538554752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927254 | CTCCCCAGGGCTCAC[C/T]GAGAATGAACAGGAA | 11060 |
rs538572544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895280 | TCAGCACTAGCCAAA[A/G]AGTCTTACCCAAGGA | 11060 |
rs538574647 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811621 | AGCTGGGCATGGTGG[G/T]CATGCAACGGTAGTC | 11060 |
rs538588984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69881816 | CCTGCCTTAGCCTCC[C/T]GAGTAGCTGGGACTA | 11060 |
rs538619683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925764 | GCAGCTGGGGGGCTA[C/T]TGGCTTTTGGTCTTG | 11060 |
rs538642824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894053 | CTTGGGGATCTCATG[A/G]CTGTATTTTTCAGGT | 11060 |
rs538653469 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826795 | CAAAAAAAAATTAGC[C/T]GGACATGGTGGCAGG | 11060 |
rs538655389 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852391 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 11060 |
rs538663777 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69926706 | GATGTTCAGCTTGGG[G/T]ATCCCTTACGCAGAT | 11060 |
rs538680416 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935707 | TCCTGAGGCCCTCCC[A/G]CTGCGTCCGAGGCAG | 11060 |
rs538785610 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69801357 | CACCTCAGCCCCCAC[A/C]CCTAGTAGCTGGGAC | 11060 |
rs538831500 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888616 | TATCGTATCAGCCCA[C/T]GGAGGAGTTGGGTTT | 11060 |
rs538855191 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69908306 | GGTAGACGAAAAAGC[C/T]TGGAGGGCCTATAGA | 11060 |
rs538866422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818794 | CTGCAAACATGGGGG[C/T]GCTCCATGGTGGCTT | 11060 |
rs538870235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812207 | AGTCTCGTTCTGGCA[C/T]CCAGGCTGGAGTGCA | 11060 |
rs538897950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798843 | TTGTAAGAGAAAGCC[C/T]CTTCTTTTTGAACGC | 11060 |
rs538907640 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69872357 | GAGTAGCTGGGACTA[C/T]AGGCGCCCACTGCCA | 11060 |
rs538909119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860894 | TGTAGTCCCCCATTC[A/G]TTCAAGGTCCTGTGT | 11060 |
rs538935546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784902 | AACAACACAGTATTT[A/G]TTACCAATGATAAAA | 11060 |
rs538937836 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910731 | GCTTCTTCTTAACCT[C/G]TCTTGTCTAGGAGGG | 11060 |
rs538954157 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916174 | CTCAAGGGCAATGGG[G/T]AGTCAATGGAAGTGT | 11060 |
rs538959550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824766 | AACTTTGCACCTGTG[C/G]CTTTTTTTTTTTTTT | 11060 |
rs538963872 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829091 | CCCAGGAGCCGTCTT[C/T]GATACCCGACCCCTC | 11060 |
rs538979685 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69776837 | CCATCTCGAAAAAAA[A/T]AAAATAAAAAAAATT | 11060 |
rs538980548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818274 | GTGCAGTGGTGTGAT[A/C]TTGGCTCACTGCAAC | 11060 |
rs538981523 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822750 | GAGGCCAACGGCAGG[G/T]AGGAGGCAGGTGCTA | 11060 |
rs539001050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69766215 | AGTCACCCTTGACTC[G/T]TCTCTTCCTCTCACA | 11060 |
rs539018705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775355 | GAAGCTGAGAGTGAC[C/T]TCCTGCTTTTCCTGT | 11060 |
rs539029782 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69816284 | GTATATTTTACCACA[A/G]TTAAAAATAATTACT | 11060 |
rs539033642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872743 | GTGCAGGGGCCATCC[C/T]GATGGGGGCCCCATT | 11060 |
rs539043922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792817 | CTATCTCAGCCTCTC[C/G]AGTAACTGGAACTAC | 11060 |
rs539046765 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794871 | AGATAGTAGCCACAG[A/G]CAATTTGTATATATT | 11060 |
rs539057847 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765695 | TGGGCTTGTTGGCAC[A/T]TGTGTCTAATTCCAG | 11060 |
rs539088521 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69767039 | AATAGGGGTTTTGTT[G/T]TTTTTTTTTTTAATC | 11060 |
rs539115228 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69790793 | GTTGGCCAGGCTGGT[A/C]TCGAACTTCTGACCT | 11060 |
rs539117029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839664 | AAAAACAACATCATG[C/T]TTTAACACAAATAAG | 11060 |
rs539126169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925136 | CTGCTCCCTGCCTCC[A/G]CCACCCTGGCACACC | 11060 |
rs539170640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872035 | AGAATAGAGGGTGGG[C/T]GTCAGAAGGCTCTAG | 11060 |
rs539178272 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69906073 | TCTTTCCTTTTCTTT[A/T]CTTTCTTTTTTTTTT | 11060 |
rs539212508 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760315 | GTACTACAAAAAGTA[A/G]AGACTAAGTGTTCAA | 11060 |
rs539219172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867812 | CTGCTTTCTGCCTGC[C/T]CTGGGGGCTGTATAA | 11060 |
rs539226430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851913 | GCTTAAATCTGGGGG[A/G]TGGAGTTTGCAGTGA | 11060 |
rs539232301 | snp | A/G | 6.63603e-05 | 0.00575984 | intron-variant | WWP2 | GRCh38.p7 | 16:69937506 | AGTGGACGATGCGCG[A/G]GGAGGGACCTGCCGG | 11060 |
rs539239332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803614 | AAAGCAAATTTGTTA[A/G]GAAAGTAAAGGAAGG | 11060 |
rs539258868 | in-del | -/T | 0.322483 | 0.239262 | intron-variant | WWP2 | GRCh38.p7 | 16:69894243 | ACTATACCCAGGCTA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs539259149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69891900 | CTGACCCTGACATCC[A/G]TTCAGTCATCAAGCC | 11060 |
rs539266579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852981 | AGTCCCTGGCTGTAG[A/G]AGATGGTTTGAAGGC | 11060 |
rs539272777 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858361 | CTCACTGCACGTAGT[A/T]GCAGCTCAATAAATA | 11060 |
rs539282260 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761429 | AATGCAAAAATTAGC[C/G]AGGCGTGGTGGTGCA | 11060 |
rs539360111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859592 | AAAAGTCATTCAGGT[C/T]CTTAGCTGAATTTAG | 11060 |
rs539360814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867305 | TTCCCCAAAGCAGCA[C/T]TGTGTGCTATGATAG | 11060 |
rs539408678 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780147 | TGGTTCCTTCCCGTC[A/G]TACTTTTATACTTTT | 11060 |
rs539423999 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941413 | AGCCTGCGTCTGCCT[C/G]TGTCGTGTGTGCTGA | 11060 |
rs539465585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858909 | GAATGCTGCTCCTTC[A/G]ACATGGGCACTGGAT | 11060 |
rs539478941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850260 | GGCGTGGTGGTGTGC[A/G]CCTGTAGTCCCAGCT | 11060 |
rs539496371 | in-del | -/CAACAACAA/CAACAACAACAACAACAACAA | 0.136532 | 0.224807 | intron-variant | WWP2 | GRCh38.p7 | 16:69783796 | CAACAACAACAACAA[lengthTooLong]CAACAACAAAATATT | 11060 |
rs539505269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808092 | TCCCATTGTCCCTTC[C/T]AGTTAATTTCTCCTC | 11060 |
rs539509647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815560 | TGGGAGGCTGAGGTG[A/G]GTGGATCACAAGGTC | 11060 |
rs539532671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69916448 | GAGCAGGAGTGTGAC[C/G]GAAGGGCTCAGTCTA | 11060 |
rs539534538 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822470 | GTTGTGACAGATGCG[A/T]TGGAGCAAAGTACAG | 11060 |
rs539550354 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808272 | CATGTGTCAATAGTC[-/T]TTTTTTTTTTTAATA | 11060 |
rs539572024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823003 | TTAGCCAGGCATGGT[G/T]GCACGTAATCTCAGC | 11060 |
rs539584520 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884017 | AAAAGCTTAGACAGT[A/G]TAAAGAATGTCTTTT | 11060 |
rs539600962 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830886 | CTGAGTTTCAGGGAA[C/T]TGGGGAATGGAAAGG | 11060 |
rs539612444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845126 | ACAAAACCTCTCGGA[G/T]CCCCAGTTTTTTTCA | 11060 |
rs539618762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936961 | CTGTGAGGTTTTCAG[A/G]GCCTCACTCTAGGTC | 11060 |
rs539658461 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931644 | AGCACCCCATCTCCT[A/G]TCGCGTGGCCTGTTA | 11060 |
rs539681785 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69810631 | AGAGATGGGGTTTCA[C/G]TGTGTTAGCCAGATA | 11060 |
rs539717225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883765 | AAACAGAAGAGCTAC[C/T]ATGGGTGAACCAGGT | 11060 |
rs539726946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851199 | TTTTTTGTATTTTTA[A/G]TAGAGATGAGGTTTC | 11060 |
rs539727427 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837053 | CTCTGCCTCCTCAGT[A/G]TCTGGGACTACAGTT | 11060 |
rs539736625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844533 | GGATCTAAATTCTTG[A/C]CCTATTTACTGGTCT | 11060 |
rs539807178 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842164 | GCTAAGAAGTTGCTT[A/C]GAGCTATTGAAAACA | 11060 |
rs539850415 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850490 | CTAGTGTGATGGATC[C/G]ATGGTGATGGTATGT | 11060 |
rs539872702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69913628 | AAGGAAAACCAGATT[A/G]TAATTGATATCCTCA | 11060 |
rs539896223 | in-del | -/CTGA | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69832769 | GGCTGGCTTGAACTC[-/CTGA]ACTCAAGTGATCTGC | 11060 |
rs539939595 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889279 | GCAGTGAGCTATGAT[C/G]ACACCACTGTACCCC | 11060 |
rs539955867 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69777690 | TTTGTATTTTATTTT[G/T]AAAATGCTTGTCAAG | 11060 |
rs539959482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765076 | AGGTGCAGTGGCGCC[C/T]GCCTGGCTACTCAGG | 11060 |
rs539968359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808923 | TCATAGGGTGGATGT[A/G]TGCTTACCTTTAGTA | 11060 |
rs540001924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69922993 | CTCCTGGGTTTAAGC[A/G]ATTATCCTGCCTCAG | 11060 |
rs540034281 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69802719 | GATTCTCCTGCCTCA[A/G]GCTTCCAAGTAGCTA | 11060 |
rs540055685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781849 | GGAAAGGCAGGAGAG[C/G]TAGAGAGAAACGTGA | 11060 |
rs540064976 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807620 | CAAGACCCTTTCTCC[-/AA]AAAAAAAAAAAAAAA | 11060 |
rs540069527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69915713 | ATTATATTCCCTGCA[A/G]TCCTGTTTATGTTTC | 11060 |
rs540071876 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69763882 | AAGTCTTCTACTCTT[C/T]TTCTTGTCAGAGAAG | 11060 |
rs540120610 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763333 | GTTATGTTCCTTAGA[A/T]CTGTGACCTGGATCA | 11060 |
rs540131555 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69820789 | ATTTTGTTCACTTTT[G/T]TGTACCTACAACACA | 11060 |
rs540146148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788183 | GCCTGAGCAACAGAG[C/T]AAGACCCCCGTCTCT | 11060 |
rs540146250 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | WWP2 | GRCh38.p7 | 16:69795261 | AAAAAAATGCGGATA[C/T]ACACACACACACACA | 11060 |
rs540163298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69884089 | TGTTGTGTTTCTTGC[A/G]GTTCTTTCAAAGATA | 11060 |
rs540187827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69899721 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 11060 |
rs540189291 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867082 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCTGA | 11060 |
rs540196202 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69806949 | TTTTATTTATTTATT[C/T]ATTTATTCATTCATT | 11060 |
rs540215929 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809390 | ACAGAGACCCTGTTT[A/C]CGGATGCGAGACTGT | 11060 |
rs540216595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778676 | AGACAGAGTCTCGCT[C/T]TGTTGCCCAGGCTGG | 11060 |
rs540247213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69900481 | TTTTAAAAAAGATAA[C/T]TAAAAGAATTTTTTA | 11060 |
rs540251835 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812282 | GCAATTCTTCCACCT[C/T]AGCCTCCTGAGTAGC | 11060 |
rs540254021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893185 | CTCTGGGACTCCCTC[C/T]CGGATCCCTGGTGGA | 11060 |
rs540260730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770884 | ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCAG | 11060 |
rs540300007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777015 | TTTAGTAAGACATAC[A/G]TTTTATATCTTAAAA | 11060 |
rs540337077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69769173 | ATACAAAAAACTAGT[C/T]AGGCGTGGTGACAGG | 11060 |
rs540363793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875598 | GGAATATTCTAAATC[A/C]TTGTTGTCATTTCAA | 11060 |
rs540382191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763719 | GGCCTCTTCCTGCTA[A/G]ATTGCAAATCCTTCA | 11060 |
rs540393168 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69791693 | TAGCTAATTCTTAAA[-/T]TTTTTTTTATAGAGA | 11060 |
rs540404185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812451 | ATCACAGGCATGAGA[C/T]ACCGCGCCTGCCCCC | 11060 |
rs540404964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926831 | CCTGCGTCGTCAGTA[A/G]GCAGGGGAAAATGCG | 11060 |
rs540410863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792053 | AAGAGAGAAATAACC[A/T]TTTAAATAGCGTAGG | 11060 |
rs540445766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807463 | TCTCTACAAAGATTT[A/T]AAAAAATTAGCTAGG | 11060 |
rs540464474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927449 | GGCCTGTGGCTGAAT[A/G]TGTCTGAGTCCCTTT | 11060 |
rs540464766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69919387 | AGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 11060 |
rs540472136 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69829672 | GGCCAAGCATCTGGC[C/T]GCTCAGGGGACCATA | 11060 |
rs540477385 | in-del | -/ATATATATATATATTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912982 | TATATATATATATAT[lengthTooLong]TTTTTTTTTTTTTTT | 11060 |
rs540483331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798009 | AGGCATGAGCCGCCA[C/T]GCCCGGCCTTAGCTG | 11060 |
rs540501681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893736 | TTTAGTAGAGCCAGG[G/T]TTTCACCATGTTGGC | 11060 |
rs540514785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833848 | TTGCCCAAAGCTTTG[A/T]TTCCAAGAGATCAGT | 11060 |
rs540542736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862314 | AGGTGATCCACTCAC[C/G]TCGGCCTCCCAAAGT | 11060 |
rs540550106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771687 | TGCTGAAAAACAATT[A/C]TCTTTTTCTCTCTGT | 11060 |
rs540550212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763196 | TGGACAGAGAAGTGT[A/C]TACCTAGACTGCTTT | 11060 |
rs540571935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906363 | AGGTGTCAGCCACCG[C/T]ACCCGGCCTTACGTA | 11060 |
rs540582886 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812080 | AGTTGTCCTGTGTCT[C/T]TAAATCTGGATCTGC | 11060 |
rs540589600 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69846049 | AGCCAGACTCCATCT[C/G]AAAAAAAAAAAAAAA | 11060 |
rs540599343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861073 | GGAGATTCCTCCTGT[G/T]CACAGTGGAGGTTGA | 11060 |
rs540609435 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938268 | GTCCTTCCATCTCAC[A/C]CTCCCAAAGTGCTGG | 11060 |
rs540642023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69812970 | GCTAGTTTCTGCATC[C/T]GGTGATTTTACTCTG | 11060 |
rs540646408 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931788 | CAGGCTGGCCCGATG[C/T]TCTGTCTTCCCAGAT | 11060 |
rs540646525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69939504 | GCAGCTTCATAGCCT[C/T]GAGTCTGGCAGCTTT | 11060 |
rs540656156 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762242 | GAGGCCAGAGGTGCC[C/T]AGGCCAGGCCTAGGT | 11060 |
rs540673462 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913835 | AGCACTTTGGGAGGG[C/T]GAGGCAGGTGGATCA | 11060 |
rs540673838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853893 | TTTAAAACCACATCT[C/T]CCATGGTGGTCGGCT | 11060 |
rs540681553 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886017 | AAGGGGGGTTGCCTA[G/T]AAACACTGAAGAAAT | 11060 |
rs540685013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69854251 | TGGTAGCTTGACCAT[A/G]TGCTGATGGAAGACC | 11060 |
rs540716227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839951 | ATACAACAGTGATTT[C/T]ATTAGACATATTCCT | 11060 |
rs540730313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818376 | CCACGCCCAGCTAAT[C/T]TTTTATTTTTAGTAG | 11060 |
rs540731828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845465 | GCTGTCTCCCAGACT[A/G]AATATTTAGCTTTTG | 11060 |
rs540782751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937302 | TCCTGCTCTGTGATA[C/T]GCTCACTGTGTACCC | 11060 |
rs540817634 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69873815 | AGATCATGGTTTCCC[C/G]CAGCTACCTCTGCTT | 11060 |
rs540819712 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69776537 | AAGTTTCTTAACTTA[A/T]AATGATAATAGGCCG | 11060 |
rs540833186 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888142 | CCCGAATCCCAACAC[A/G]ACTTCTCTCCCTGCC | 11060 |
rs540878068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805706 | GCCTCTACCTCCCAG[A/G]CTCAAGCAATCCTCC | 11060 |
rs540879868 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930575 | GTGGTGGTGCATGCC[G/T]GTAGTCCCAGCTACA | 11060 |
rs540937824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69790288 | CAGTTGATTAACACG[C/T]ATTTTGTATGTTACA | 11060 |
rs540950286 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69832124 | GTGAGCCACTGCGCC[C/G]TGCCTTCTTTGTTTG | 11060 |
rs540974480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69783643 | GAAGGTATTAATGAT[A/G]TTGAATAGAACAGGA | 11060 |
rs540980368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839220 | GGAGTGGACGGACCC[C/T]GTGGAAATCCTCATA | 11060 |
rs540982777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921740 | ACGGGACTATCACAC[A/G]GCCGACAATTTCTGG | 11060 |
rs541059948 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941366 | GTCTCCATGCTCCCA[A/G]ATTCTCGACCTTCCC | 11060 |
rs541062394 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765421 | AAGAAAGGTAAGGAT[A/C]CCCACCCTTGTGGAT | 11060 |
rs541086331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803179 | GGCTGAATTATTTTT[A/G]TTTTCTTATTTTTTA | 11060 |
rs541102560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898513 | TGTGGGCCAGTCTAA[C/T]GGGCATGAATGGTAC | 11060 |
rs541112683 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824062 | TCCTTCCCCTTGCCA[A/G]AAACAAAACTGAAAC | 11060 |
rs541129895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884168 | CACATGTGTATGCAC[A/G]CAAACTCACAAATGA | 11060 |
rs541132542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923151 | CGCCTCAGACTCCCA[A/G]AGTGCTGGGATCACC | 11060 |
rs541152416 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837888 | TCACAGCCCAAAAAA[C/G]TCTCAGAAGGATCAG | 11060 |
rs541166990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915364 | AATACCTATATCCTC[A/C]TCCCTCATCTTTGGT | 11060 |
rs541170400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885594 | TTTACATGGTTGCTA[A/G]GAGTTATTATAATCT | 11060 |
rs541173771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69803873 | AGATTGTGCCACTGC[A/G]GTCCAGCCTGGATGA | 11060 |
rs541196400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918176 | CCTTCATTCAAGTCC[A/G]TTTTCCCTGACTTGC | 11060 |
rs541201253 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69784097 | TCTTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 11060 |
rs541235140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817877 | TTGGGATTACAGGTG[A/T]GAGCCATTGTGCCCA | 11060 |
rs541296132 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69810415 | ATGTTGCCAGTTCAG[-/T]TTTTTTAACATCTTT | 11060 |
rs541341746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69858432 | CGCCAAAACTTCTGG[G/T]TGGGTCATGTTGCTG | 11060 |
rs541351427 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941801 | AAGAGGACTCCGGGC[C/T]TCACAGACCCTCCAG | 11060 |
rs541370829 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848339 | CCTGTAATCCCGGCT[A/G]CGTGGGGAGCTGAGG | 11060 |
rs541378793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865895 | ATGCCGGTCAGTTGC[C/T]GTGTGGAAACCACAA | 11060 |
rs541397122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816954 | GGAGTTCTCAGAGTT[A/G]GGATTTAACCCAGTT | 11060 |
rs541442159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69863722 | GTGCCCCTTTGTAGC[C/T]AGCTCCTCCTTGTAC | 11060 |
rs541449197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69903127 | GACATTGAGCTTTGC[A/G]GGACAATAATAGTCC | 11060 |
rs541450527 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940609 | AAACTCCCTCAGACT[C/T]TGTCCATGTATAAAC | 11060 |
rs541472196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788338 | CAGAAAAAAAAATGT[A/G]AGCTGGGTCTTGTCA | 11060 |
rs541474784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69895692 | ATAAGTCCCGGAAGT[C/T]GAGCCTGTAGTGAGC | 11060 |
rs541497529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765444 | TTGTGGATCTTCAAT[G/T]TTATTAGAGAAGGGC | 11060 |
rs541502194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877610 | CAGCTTTGGCCTGTC[C/T]TGGCTTTCAACCCAC | 11060 |
rs541514599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908054 | CAGACCAGCCTGGGC[A/G]ACATGGTGAAACCCG | 11060 |
rs541515644 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927617 | AGCCCGCTGGACAGA[A/T]CCCCCTGGCCCTGTG | 11060 |
rs541515873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862416 | CACCTAGGCTGGAGC[A/G]CAGCAGCAGGATCTC | 11060 |
rs541558737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814260 | CGAACTCCTGGGCTC[A/G]AGCGATCCTCTTGCC | 11060 |
rs541583570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781401 | CCCAGGCTGGAGTGC[C/G]GTGGCACAATCTTGG | 11060 |
rs541589728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904603 | CTCAAACTCCTGGTT[C/T]CAAGTGATCCTCCTG | 11060 |
rs541604671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929878 | CTGGGGCACAGGGTG[C/T]CTCAGGATTGCTGGT | 11060 |
rs541628091 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897619 | CAGCTAGAAAGAATG[G/T]CTGCAGTAGGCCAGG | 11060 |
rs541638422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767344 | GACCCTCACGAGGTC[A/G]GATAGCTAAGAAATG | 11060 |
rs541657111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897839 | TTTGAACCAGGGAGG[C/T]GGAGGTTACAGTGAG | 11060 |
rs541661304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890969 | GCTCCCCACTTGAAC[A/G]TGTACGATGGTCCAG | 11060 |
rs541665966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922330 | CTCAGCTGTATTTGC[C/T]AGACATTCTTTATTT | 11060 |
rs541666015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930743 | TCGGTGTGGTAGCAC[A/C]CTCCTGTAGTCCTAG | 11060 |
rs541679984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800472 | CCAATATACTTTTGC[C/T]TTTGGTTAGCAAAAG | 11060 |
rs541685120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844664 | GCAGCCAGGCTGCAA[A/C]AGGAAATCGGATGCA | 11060 |
rs541708170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69896392 | TACCAAAGTGCTGGG[G/T]TTACAGGTGTGAACC | 11060 |
rs541710419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816484 | TATATACTTTATATA[C/T]GTAATATATAAACAT | 11060 |
rs541712283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809088 | ATTGTTTGTGGTATT[A/G]GTTGTAGCTATTGCT | 11060 |
rs541715159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69774978 | TCTCAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 11060 |
rs541720559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766343 | AACTTGTCTCCCTCT[C/T]CCACCCTGGCTGGCC | 11060 |
rs541755857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775524 | TCTTATAGTTGCTAT[A/G]TCTCTCCTTACATTG | 11060 |
rs541768851 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861338 | GTAGATTGGACAAGT[C/T]ACCATTTACTATACC | 11060 |
rs541827453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857013 | TCATTTATGTTTCTC[A/G]TGATTCTTGATATCT | 11060 |
rs541875306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792912 | CCCAGGCTTGTCTCG[A/C]ACTCCTGGGCTCAGG | 11060 |
rs541878973 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790796 | GGCCAGGCTGGTCTC[A/G]AACTTCTGACCTCAA | 11060 |
rs541886617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857516 | CATCCAGTGGTGTGA[A/G]GAGAGCAAGAGCTCA | 11060 |
rs541927192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863255 | AATTATTAAGTTACT[A/G]TAATTTACAAACAGT | 11060 |
rs541943532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815085 | TTGGCTCACTGCAAC[C/T]TTCGCTTCCTGGGTT | 11060 |
rs541944680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894324 | GGGCTCAAGCGATCT[C/T]CCCGCCTTGGCCTCC | 11060 |
rs541960974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848186 | TGGCTCAGCGTGCAG[A/G]CTGGGTGTAATCCCA | 11060 |
rs541974127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844218 | ATAGTTGGGTCTCAC[G/T]GGGTGATGAATGACA | 11060 |
rs542022407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913770 | AAAATTCAGTAGAAT[G/T]GTTGAAAGGTAAATT | 11060 |
rs542047044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907542 | ATTAATATCCTTGAG[A/G]AAGTGGTAAGCATTA | 11060 |
rs542055820 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837393 | TTGAAGACAAAATGT[A/G]TCTCAAGGTGTTGTA | 11060 |
rs542105134 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859104 | CACCACAAACTCAGG[A/G]CTTAAAACAACACCA | 11060 |
rs542119221 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835750 | TGCATATATCATTCT[C/T]ATCTACTCTTGCGTC | 11060 |
rs542143358 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831810 | CTTAGGCATGCTGGC[A/C]TGGAAAAAAACAAAA | 11060 |
rs542144799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883026 | GGCGTGGTGGCACTC[A/G]CTTGTAATCCCAGCT | 11060 |
rs542156678 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872221 | ATAAAAAGAAATGTC[-/T]TTTTTTTTTTTTTGA | 11060 |
rs542163801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920740 | TGCAGTGACCTATAA[C/T]AGTGCCACTGCACTC | 11060 |
rs542180447 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830300 | TCTCACTTTGTTGCC[C/T]AGGCTGGTCCCAAAC | 11060 |
rs542191488 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867877 | GGCCAAGGTTGAAGT[A/C]ATGGGCAGAGCCGAG | 11060 |
rs542200949 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776814 | GCCTGGGCAACAAGA[C/G]CGAAATTCCATCTCG | 11060 |
rs542209272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888909 | TATGGTTTCGCCCTG[C/T]TGGCCAGGCTGGTCT | 11060 |
rs542225549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69934239 | TCTTTCTCTGAGACC[G/T]CCAGGAAGGGGCAGC | 11060 |
rs542225604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927746 | TGGGAAGCCTTCCTT[C/T]TGTGTGTTCTGAGGT | 11060 |
rs542249767 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69888722 | TCCTTTTTTTTTTTT[A/T]GAGATGGAGTCTTAA | 11060 |
rs542250134 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802931 | ATTATGTATGTGCAA[A/C]TATACCAAAATCTGA | 11060 |
rs542260211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799600 | CAGGAGATGTGTGAT[A/G]TGTTGAATGAAACTG | 11060 |
rs542288952 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826938 | GCGAGACTCCACCTC[-/A]AAAAAAAAAAAAAAA | 11060 |
rs542290974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834967 | GCCCATCTTGTTCCT[A/G]TTGAGTCACTAGAAT | 11060 |
rs542311148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791246 | TCTTTTTTTTTTTTT[A/G]AGACGGAGTCTCGCT | 11060 |
rs542326585 | snp | C/T | 1.6902e-05 | 0.00290701 | missense | WWP2 | GRCh38.p7 | 16:69939909 | AGCTGCTGTATGCCA[C/T]TGAGGAGACCGAGGG | 11060 |
rs542415709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836257 | ATGGCATTTGTTGGT[G/T]TTCTTTAGATCTAGA | 11060 |
rs542451174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854842 | AAGTGTGGGCCACCG[C/T]GCCTAGCCTCTTTTT | 11060 |
rs542451426 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925805 | TGTCTACTCAAGAGT[C/T]CATGCTACCACTAAG | 11060 |
rs542456250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762415 | CGCTGGCGCGGGGGG[C/T]GCGGTGGGCTGGCTG | 11060 |
rs542491666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826788 | AAAAATACAAAAAAA[A/C]ATTAGCCGGACATGG | 11060 |
rs542507229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868238 | TTCATGCAAAGTGAT[C/T]CCAGCTGCCCCTAGC | 11060 |
rs542526617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861242 | AGGTGAACACTTCCC[C/T]TCTGAACTCTCTAGC | 11060 |
rs542528041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69835629 | TTATAGTATATGGCT[A/G]GGTGTATTTTTTTTC | 11060 |
rs542535572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819373 | GTGTCTGCTACTCCT[G/T]TGTTACCTCATCTCA | 11060 |
rs542609617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912468 | TAGGAGGACCAGGTC[A/G]GGGGACACAAACTAT | 11060 |
rs542620006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817738 | ATCACAGCTCATTGC[A/G]GCCTTGACCTCCCAG | 11060 |
rs542620136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928872 | ATGAGAGTTTTAGAA[C/T]AAGACTTAGCCTGTA | 11060 |
rs542628634 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777109 | ATATATACACATATG[G/T]GTATATACAATACAC | 11060 |
rs542631056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69847700 | GCTGTGAGCCACCGC[A/G]CCTGGCCAGGCTCTT | 11060 |
rs542658914 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891679 | CTCAGCCATTCCCTT[G/T]GCTGCCTCTGGGATC | 11060 |
rs542662374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798426 | AGGCAATTTACCAAC[A/G]ATAAATTGGTGATGA | 11060 |
rs542684705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783477 | GAAGTTCGAGGCTGC[C/T]GTGAGCCATGATTAT | 11060 |
rs542708427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880751 | TTGCTTGTGTTTCAC[A/G]GGTGAAAGACACCAA | 11060 |
rs542710198 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69872794 | CACGTGCGCATGGAA[A/C]TTCCCCACACTTGGC | 11060 |
rs542710324 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887541 | CTCCCAACTAGCTGG[C/G]ATTATAGGTGTGCGC | 11060 |
rs542711259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910247 | AAATAAAACTCTAAT[A/G]TCATTAACAGTATTT | 11060 |
rs542723130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776365 | TGACTCTTTACCAGG[A/T]TAATCTTGTAAAGAA | 11060 |
rs542732137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874189 | GTGATGGTGGTTCAC[C/G]TTTACCTCACAGGCA | 11060 |
rs542732679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824036 | AGATTGTTGCCTGAA[C/T]GTGAGCTGTTTCCTT | 11060 |
rs542739383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867684 | GAGAGAGGACCTTGA[G/T]TGAGGACACACCGCA | 11060 |
rs542773871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881261 | CCACTGTTTTTACTT[A/C]GTGGTGTTCTGGTTT | 11060 |
rs542790338 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69784378 | GCGCTGGGAATACAG[G/T]CGTGAGCCACTGTGC | 11060 |
rs542804447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906956 | TGAGTAGGAATGTAA[C/T]ACTAAAAATATTTGT | 11060 |
rs542805823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770832 | CTCCCACACATCTGG[C/T]GTCAGAAGTATTCTG | 11060 |
rs542816420 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69846763 | GGAATAATGAATCCT[A/G]AATTCAGGAGGTTAT | 11060 |
rs542844237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762987 | GTAGGGTTTCCACTT[C/T]TTGGGAGCCTAGCCC | 11060 |
rs542856085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932991 | GGCGTTGCCTTCTGC[A/G]CTGGCCCCGTGGATG | 11060 |
rs542868069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901464 | GTCGCCCAGTCTGGG[G/T]TGCAGTGGCGCGATC | 11060 |
rs542869412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797875 | CCTGGGCAACAAGAG[A/C]CAAACTCTATCTCAG | 11060 |
rs542884406 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69938944 | CCCAAAGAGGGGCCC[C/T]GCTGAGCTAGAGAGC | 11060 |
rs542902065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840904 | CCAGACACCAAGCAG[G/T]ATTTCTGTAGCTTCA | 11060 |
rs542905541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912502 | TGAAGGCCAGGATGA[A/G]CTCAGAAACAAGAGA | 11060 |
rs542907140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812318 | TTACAGGCACCCACC[A/G]TCATGCCCAGCTAAT | 11060 |
rs542907262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804100 | TCTTTATTTGTTAAG[G/T]TTATTATTCTTCGTC | 11060 |
rs542926217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868847 | CCCATGAAGTGGGAA[A/C]TTTGAAATATTCATC | 11060 |
rs542937116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69899654 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 11060 |
rs542944350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804838 | TTCTAAATTAATTCA[A/G]ATAATTTTGAAGTTA | 11060 |
rs542991941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893106 | TCACTCTTTCTGAAA[C/G]CTTCCTTGCCATCTT | 11060 |
rs543017920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69884397 | GGGAGGCTGAGGTGG[A/G]AGGATCGCTTGAGCT | 11060 |
rs543021220 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69859891 | CCCCGCCCGATGATC[A/C]CCTTTCTTAAGGTCT | 11060 |
rs543030511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898694 | AATCTGCAGGATTCT[C/T]TTTTGTTGTTGTTTT | 11060 |
rs543042793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769108 | TGGATCATGAGGTCA[C/G]GAGATCGAGACCATC | 11060 |
rs543072918 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941610 | GCGTGTGTGTGCGTA[C/T]GTGTATATAACTGAA | 11060 |
rs543100423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845334 | AAGTGAGGCATTACC[G/T]GTGCGTTTACATCAA | 11060 |
rs543120254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69767682 | GTGCTGGAGGGGGCT[A/G]TGTGGGGATTGATGC | 11060 |
rs543171987 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919259 | TAACCTCCACTGCCC[A/G]GGTTCAAGCAATTCT | 11060 |
rs543223222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925232 | CGCAGGGTTCTTTTT[C/T]GGTTTTTCTGTAAAA | 11060 |
rs543266819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789038 | ATACTCATGGAGTTT[A/T]AAAATCTTAGTTTTT | 11060 |
rs543288457 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69917531 | GAAATTGAGAGCTAA[A/T]GGCAAGGAGGGATTG | 11060 |
rs543322373 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911244 | TGGGTCCTTCTATCC[A/G]GGAGCAATAAGTATT | 11060 |
rs543343443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69853208 | GGTATTTTGAGCAGA[A/C]AAGGATTTAATATGG | 11060 |
rs543364566 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837232 | GCCTGGCTGGCTGCT[C/T]TTAATTAATTTTTTT | 11060 |
rs543394050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844763 | AGTGTAAGCCTTATC[A/G]GAGTCCTCTGCAGTC | 11060 |
rs543420717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69795788 | GAGTAGCTGGGACTA[C/T]TGTTGTGCCCCACCA | 11060 |
rs543424653 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936611 | GTCATGTGATGGCGC[A/C/G]AGCTGGGGGAACCAA | 11060 |
rs543426268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930894 | CGAACAAACAAATAA[A/G]TAAGATGGGATGGGG | 11060 |
rs543436703 | snp | C/T | 0.0111196 | 0.0737302 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941847 | GAAATTCCCTGACCT[C/T]GCTGGTTTTGAGAAG | 11060 |
rs543455268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803129 | ATTTGATAACTATTA[A/G]CATTATGATGGATTT | 11060 |
rs543461752 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941780 | CAAAGCCACAGTCCT[C/T]CAGTCAAGAGGACTC | 11060 |
rs543468715 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894075 | TTTTCAGGTTGCTGC[A/G]TTTTTTTTTTTTTTA | 11060 |
rs543517348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929703 | GTTGGCCTGATGAGA[C/G]CTTAAAAGGGGTTTC | 11060 |
rs543529712 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896046 | GATTCTACTGTTGTC[A/G]GAGGCTGGGCCATGA | 11060 |
rs543530705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802499 | GCTTATGTTAGTGGA[A/G]CCATACAGTATTTGT | 11060 |
rs543536475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809982 | GAGTGGTGTCAAATC[A/G]TGCATACAGTTGTGT | 11060 |
rs543544978 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69891053 | CTCTAAGATGGCTAG[G/T]AGGGCTCTGTGGGCT | 11060 |
rs543562136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844194 | CCGTGTCTCGGTAGG[G/T]GACTTACAATAGTTG | 11060 |
rs543562374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936170 | TCTAGAACCTTCTCC[C/T]TGAGTCAAGGAGCTG | 11060 |
rs543574469 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917197 | AATCCTGATTCCAAG[C/G]GAAGCTTGGGCTACT | 11060 |
rs543575855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916758 | GGGTGACAGCTGGTC[A/T]TGAAGGTGAGGCACT | 11060 |
rs543592872 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772519 | CAGAGTTACAGCTCC[A/G]TGACTGCTCCTGCAG | 11060 |
rs543593032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831434 | AGTAGCATGGTCTGG[A/C]AGTTACAGTTTATGT | 11060 |
rs543615244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822526 | GACTTTGCCTGGCCT[G/T]GGTGGGGTGTGTGTG | 11060 |
rs543648291 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69858228 | CCACCTGGTTTGTGG[G/T]TTTTTTGGGGAGGAA | 11060 |
rs543655390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816446 | CTATATCTATAACTA[C/T]ATCTATATAATATAT | 11060 |
rs543680369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832078 | AAGCGAACCATCTGC[C/T]TCGGCCTCCCAAAGT | 11060 |
rs543690220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69766288 | ACTTCAGAGTACACC[C/G]TGGATGCATCTTTCC | 11060 |
rs543709370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924395 | GATCCCCTCTTATAA[C/T]GATTAAATTTTAGTA | 11060 |
rs543759606 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69915744 | AAAACTATATACATA[G/T]GACTTCGGGCCGGGT | 11060 |
rs543770254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922270 | AAAAAAAAATGCCTG[C/T]GTTCCACGCTGCAAC | 11060 |
rs543815261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69788252 | TGAGCCTAGGAGTTC[A/G]AGGCTGCAGTAAGCT | 11060 |
rs543824062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69907968 | ACTTTAAGCCGGGTG[C/T]GGTGGCTCACTCCTG | 11060 |
rs543838924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829578 | TCCTCCCTGCCCTGC[C/G]CTACCCTGCTAGCTG | 11060 |
rs543884948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902075 | TTCAAACAGGTGAAT[A/C]TGACCAAGAAATATG | 11060 |
rs543903331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69890277 | CCTAGCATGCGCCAC[A/G]CTACCTAACTCCCGT | 11060 |
rs543905159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883292 | GTTGACCAGGGTGAC[C/T]GTGGGCCAGTAATGT | 11060 |
rs543945846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778735 | CAACGTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 11060 |
rs543953608 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WWP2 | GRCh38.p7 | 16:69820328 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 11060 |
rs543965562 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827666 | TAAACATGGCTTTGA[A/T]ACCAGGCAACTGAGA | 11060 |
rs543966328 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907348 | AGCAAATAGAATTCC[C/T]ATTATGCTCACATCG | 11060 |
rs543994209 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69765626 | GTCAGGATTTCAAGA[C/G]CAGCCTGACCAACAT | 11060 |
rs543994990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909090 | CAAGATTTAGAGTGT[A/T]GATGCATTCCGCCGT | 11060 |
rs544036276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809250 | CTAGGATGACAATGG[C/T]GTACGTAGCCTATGT | 11060 |
rs544049636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843582 | TAAAATCTTCCCAAA[C/T]GAGGCCAGGCACAGT | 11060 |
rs544050755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932912 | GCTCGAGACCTCTCC[C/T]GGTGTGGGCATGTCT | 11060 |
rs544052629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903880 | CACCCAAATATTAGA[A/G]TTTTCCAAATAGTGA | 11060 |
rs544070352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822093 | GCTGGTCTCAAACTC[A/G]TGGGCTCAAGCGATC | 11060 |
rs544070463 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69765851 | TGGGGAGTTGGGGGC[-/G]GGGGGTTCTCACTTT | 11060 |
rs544081943 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863811 | ATATCTTAAAAATGG[A/G]AATGTACACGTATAG | 11060 |
rs544091336 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786865 | ATAAGACAAACTATA[A/C]CCTGGTTGCAGTTGC | 11060 |
rs544102890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781325 | GTCAAAGTTCATTTG[C/T]AGGTCTTTGGCTTTT | 11060 |
rs544106353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774198 | ATTCTTTCCATCTTA[A/C]ATTTCCACCCAACAT | 11060 |
rs544162759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69820861 | ACACACACACACGAC[A/G]TTGAAAGAGTGACTT | 11060 |
rs544185332 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69771907 | AACTATGCCTGAAGT[C/G]TTGAGTTTGGTTTCA | 11060 |
rs544206669 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69894286 | GGGTCTCACTCTGTT[G/T]CCCATGCGGATCTCA | 11060 |
rs544224501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862355 | CAGGCGTGAGCTACC[C/G]CGCCTGGCCCTTGTT | 11060 |
rs544252626 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834917 | TGTCTGTTTCTGCCA[A/G]GTAGAATGTAAATGC | 11060 |
rs544262358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69861212 | TACCTCAAGCCATCA[A/G]TGGCCACGTTGAGCA | 11060 |
rs544266870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847627 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 11060 |
rs544273931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69828019 | TGGGGTACCTTGTTA[C/T]GTGGGTGACTGTAAT | 11060 |
rs544360831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783335 | ATTCTTAGAGTAATA[C/T]GGTGAATTAATAACC | 11060 |
rs544388754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785751 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11060 |
rs544396839 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857205 | GCCTCTGGGGTTCAA[A/G]CGATTCTCCTGCCTC | 11060 |
rs544401916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853977 | GTCATTTCTCTGAAA[A/G]TGCACCCATAGGAGG | 11060 |
rs544407074 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881243 | TGTCTTCGCTCCCCA[C/G]GCCCACTGTTTTTAC | 11060 |
rs544407896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805845 | GTTGACTTTGTATCA[A/G]ATATCTATTAAGCAG | 11060 |
rs544447696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920219 | GACCTCAGTTTCCTT[A/G]GCAGAGGTGAGCAGA | 11060 |
rs544470180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875685 | TGCTCATCCATAAGA[C/G]ACAACTCCTAATCTA | 11060 |
rs544471484 | snp | A/G | 0.000115337 | 0.00759312 | missense | WWP2 | GRCh38.p7 | 16:69888170 | GCCCCAGCCACACCG[A/G]CTGAAGGAGAGGAAC | 11060 |
rs544478789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902765 | ATGGGGGGGACCAAA[C/T]CAAGACAGTCGGAGG | 11060 |
rs544479062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863169 | CTGTTTTTTTGACCA[C/T]ACCCTCACGCCATAC | 11060 |
rs544515365 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940567 | GGTTTGTCTAAGCTG[C/T]CTGGGTATCCACGGG | 11060 |
rs544540109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895562 | TGAGTCCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 11060 |
rs544542898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792782 | CTACAGCCTCGACCT[A/C]CTGGGCTCCAGGGAT | 11060 |
rs544559320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840727 | GTCCCTTGCTCTGTC[C/T]CGAATGTTGGTAGTT | 11060 |
rs544566420 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807080 | TTTGCCCAGGATGGA[A/G]TGCAATGGCATGATC | 11060 |
rs544580814 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69854771 | GGTCATGCTGGTCTC[C/G]AACTCCTGACCTCAG | 11060 |
rs544586306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69927639 | GGCCCTGTGGTTAGC[C/T]TTGGCTTTGGCCCTT | 11060 |
rs544609297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806664 | TTTTCTGAGAAAATC[A/G]GTTCATGAGATTTTC | 11060 |
rs544629595 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793789 | TCCTGAGCAGTAAGG[A/G]ATTATAGAAACTATA | 11060 |
rs544663115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933705 | AAAGTCTTGGAACAC[A/G]TCACCTGGGAGCCGA | 11060 |
rs544701350 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832204 | GAACAAAAACTGTTA[G/T]AGGAAATGTGAAACA | 11060 |
rs544703107 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859534 | GCACTCCAGCCTGGG[C/T]GACAGAGGGAGACCC | 11060 |
rs544720599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839994 | TTCCATGCCACGAGG[C/T]AAAATGTGAAGATGT | 11060 |
rs544724499 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858480 | CTTGACTCCTGAGAT[-/G]GCGATAATTTGAGGA | 11060 |
rs544738685 | snp | A/T | 0.000408873 | 0.0142923 | intron-variant | WWP2 | GRCh38.p7 | 16:69939004 | TGGGTTGCCTGACTG[A/T]GCCTTGACTTGCGGA | 11060 |
rs544739732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69797313 | CTGGTAATCGAAGAA[C/T]AGCAATAGAACAAAT | 11060 |
rs544768550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834676 | GGATTACAGGTGCCC[G/T]CTACCACACCCAGCT | 11060 |
rs544786466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932420 | GGGTGCCCCACTGGG[C/G]TGGACATTAAGCCTT | 11060 |
rs544802636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868029 | AGTTCTCCAAGAGAG[A/G]AAACTGCCAAAGAGA | 11060 |
rs544827555 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69920614 | CCTGATTATCCAAAA[A/T]TTCTCATTAAAAAAA | 11060 |
rs544829368 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761960 | CATATTACACTGTTG[C/T]TTATCTGAAATTCAA | 11060 |
rs544865475 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771341 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCTATTCT | 11060 |
rs544867248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769202 | GGCACCTGTAATCCC[C/T]GCTACTCGGAAGGCT | 11060 |
rs544897467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906420 | GCTGATCAATGCAGT[C/T]CACTAACCAGACATC | 11060 |
rs544903055 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896175 | CACCCAGGCTGGAGT[A/G]TAGTGGCGTGATCAT | 11060 |
rs544937207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867640 | GGTCCTGGTCGTGGC[A/T]GGCCTGCCTTCAGGA | 11060 |
rs544959699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909705 | ATGGACTTCTCAAAT[C/T]AGAAAAAAACAAACA | 11060 |
rs545004617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817161 | GGGAACTCATTATAC[A/G]TATTTCTTTGTAACT | 11060 |
rs545005888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842715 | TGCTTTGTTGCCTAC[A/G]CTGGAGTGCTATGGC | 11060 |
rs545007140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791152 | GAAGTTGGCCTATTG[A/G]ACCTGGTAACATCCT | 11060 |
rs545041089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69823281 | TTTGGCCTCAGGTGT[C/G]TCTTTCTGACACACA | 11060 |
rs545106111 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848167 | AGCTGTCAGCTGGGC[A/G]CAGTGGCTCAGCGTG | 11060 |
rs545107988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892951 | ATAAGGCCTAAAAAG[C/G]CCTGTGTAATATGAC | 11060 |
rs545108048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886152 | CAGTGGTGCAATCAT[G/T]GCTCACTTCAGCCTC | 11060 |
rs545118129 | snp | A/G | | | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934054 | GAACAATTACTGCCT[A/G]CAGATCAACCCCGCC | 11060 |
rs545148010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906194 | TCTCCTCCCTCAGCC[C/T]CCCAAGTAGCTGGGA | 11060 |
rs545151695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831311 | TCGGTGGTATGGGGT[A/G]GGGAGGGACAATAAT | 11060 |
rs545154280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826051 | GTGGGCAGATCACCT[A/G]AGGTCAGGAGTTTGA | 11060 |
rs545165357 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849816 | CTGTCTCTTAAAAAA[A/T]AAATCATGGAGATTA | 11060 |
rs545178740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777508 | GTTTCACCCTGTTGG[C/T]GAGGCTGGTCTCGAA | 11060 |
rs545183173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937483 | TGGGGTAATGTCAAG[G/T]GCTAGCGAGTGGACG | 11060 |
rs545191957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818454 | TCAAGTGATCTGCCT[A/G]CCTCAGCCTCCCAAA | 11060 |
rs545227348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898667 | TATTTGTCTTTATAT[A/G]TATTTATTTTTAATC | 11060 |
rs545242760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846354 | TAGTAGGATGTCATA[C/T]GTAGAAAGTTGAAAA | 11060 |
rs545259366 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918431 | CTGCCACTTCATTTT[G/T]TTAATAAAGTTTCAT | 11060 |
rs545260756 | in-del | -/TTAGGGTTT | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69793487 | CTGGAGGCTCAGAGA[-/TTAGGGTTT]TTATAGACAATTTGA | 11060 |
rs545319434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919096 | TGACCTGCCCTCCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs545343922 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916890 | TCATTGAGGCCGGGT[A/G]CAGTGGCTCACGCCT | 11060 |
rs545345905 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941063 | CGCCAGCGGAAAGTG[C/T]TCATTCTGCATAGGT | 11060 |
rs545349312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896469 | AAGAATATTGTGTCC[A/G]TCTTTGTGTTCCCTG | 11060 |
rs545368689 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891029 | CCCAGATGGCTTCCA[C/T]GTGCTCTTCTCTAAG | 11060 |
rs545397927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859834 | CTTCCAGGAGGTGAT[A/G]TGATGCTAATTAGAC | 11060 |
rs545415566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890510 | GAAAGACCTTTGTTT[C/G]GTTTGTAATTTCAAG | 11060 |
rs545420724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866025 | TGGCTAGGGAAGGAG[C/G]GGGTGTAACGAGGTG | 11060 |
rs545435275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903691 | GGGAATCGGTTGAAC[C/T]CAGGAGGTGGAGGTT | 11060 |
rs545450392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69863912 | TTCCTTTTATGCATT[A/G]AGTTTATTCCACTAT | 11060 |
rs545465990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858118 | ACCTTTAGAACCAGT[A/T]AAAAAAAAAAGTTTT | 11060 |
rs545488819 | snp | A/G | 3.3592e-05 | 0.00409815 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871819 | GACGCACAGACATTC[A/G]GGTGCTTCAGCCAGA | 11060 |
rs545505960 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909638 | GTCATCATCAGTACT[C/T]ACTGTGTTTTCCACT | 11060 |
rs545506107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809881 | GAAAAAGCTTTGAGG[A/G]TGTGGAGTGGGGAAG | 11060 |
rs545518795 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925689 | CAAGCTCCACCGAAC[A/C]ACTGTAGCATCCACC | 11060 |
rs545524836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850491 | TAGTGTGATGGATCC[A/G]TGGTGATGGTATGTA | 11060 |
rs545578460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788914 | GATGGGAGAGTGGCT[C/T]TCAGTATCTGAGCTC | 11060 |
rs545584822 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869396 | AAAAACTTAATTTTT[C/T]TTTTTTGTTAAACAA | 11060 |
rs545602708 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69762627 | TGCTCCGAAATGGGT[G/T]CCCCGGCCGCCAAGG | 11060 |
rs545627189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69916127 | AGGTTCCAGATTTTT[A/G]TGAGCCTTGTGTACT | 11060 |
rs545645158 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858546 | CCTTGTGCTTGCAAG[G/T]TGAACCACCAAGAGT | 11060 |
rs545653230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931293 | TCAGTGTGAGTTCCC[A/G]GCACAGCAGCAGGTA | 11060 |
rs545672998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866859 | TTATTTATTTTTGAG[A/G]CGGAGTCTCGCTCTG | 11060 |
rs545676411 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69891019 | AATTTTCCAACCCAG[A/T]TGGCTTCCACGTGCT | 11060 |
rs545710355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803282 | ATCCTAGATTCTTCA[A/G]CATGCATCTTGTTAA | 11060 |
rs545718379 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP2 | GRCh38.p7 | 16:69882508 | TAAGGCCTCTGCCCT[A/G]TGATCTTGTTCCAGA | 11060 |
rs545733937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768484 | GCGTGGTGGCAGACA[A/C]CTGTAATCCCAGCTA | 11060 |
rs545739645 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69795581 | AAATGATAACAATTG[A/G]TGAAGAGTATACAGT | 11060 |
rs545760384 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69843410 | AGTATAAAGAGATGA[A/G]GGGAGAGGGTTGGCA | 11060 |
rs545780322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882042 | CCAAGCTGGTCTCGA[A/G]CTCCTGGCTTCAAAT | 11060 |
rs545799517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69850115 | AAGTCGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 11060 |
rs545799806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935526 | GCCTTTTCTGTGAGC[A/G]TGGGGCAGACCTTTG | 11060 |
rs545806173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801321 | ACCGTAGCCTCTGCT[C/G]CTGGGCTCAAGTGAT | 11060 |
rs545835173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835763 | CTCATCTACTCTTGC[A/G]TCTCCCAAGAATAAG | 11060 |
rs545877575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903176 | TTTCCAGCATCAGCC[A/G]TGATCAAAGATGGAA | 11060 |
rs545899634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842906 | ACTCCTGGACTCAAC[C/T]GATTCTCCTGTCCTG | 11060 |
rs545909630 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69815902 | AGCTAAGACTACAGG[C/T]GTGTGCCACCATACC | 11060 |
rs545952707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923332 | GGGTGGGGGGGGTGC[A/G]TTCTGATAGAATAAC | 11060 |
rs545964313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888957 | ATCATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs545986213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870498 | TAGAGGCAGGGTCTC[A/G]TTATGTTGCCCAGGC | 11060 |
rs546047773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908108 | AAAATAGCTGGGCAT[C/G]GTAATGTGTGCCTGT | 11060 |
rs546062943 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838770 | GTACTCACCAAGGCC[C/T]TCAGTGGAACTGGCT | 11060 |
rs546067378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69880120 | TATAGTGTTATATGT[A/G]TCACTATAATATATA | 11060 |
rs546072963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69781170 | GGAGTCTGTCTGCAC[A/G]TTCAAGGGATAGTTG | 11060 |
rs546075044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863371 | AAGGCTGGGCGTGAT[G/T]GCTCATGCCTGTAAT | 11060 |
rs546095889 | in-del | -/ATTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778961 | TTTATTTATTTATTT[-/ATTT]TTTGAGATGGAGTCT | 11060 |
rs546099280 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69806461 | TTCCAACTTTGGGAA[C/T]AGTCTCTATAACATG | 11060 |
rs546124818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884265 | TTGAAGCTAACTTGA[A/G]GAGCTTCGTTCACCT | 11060 |
rs546125067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869940 | AATGGGGAACTTTCT[A/T]TTATAGCTCTTAATT | 11060 |
rs546143620 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69863886 | CTGTTGCTGCATGTA[-/C]CAGCACTTTATTCCT | 11060 |
rs546154217 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813441 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 11060 |
rs546157042 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69929301 | GTGACAAGTGTGAGT[G/T]AGCTTGGCTTTGGCT | 11060 |
rs546184765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69853641 | AGACTCAGGGACTGA[C/T]GAAGAGGACTGTTGC | 11060 |
rs546189933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69883241 | AGTTTTTCTATTTGA[A/C]GCCTCATTAGACTTG | 11060 |
rs546217310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877423 | TTAAGAGAATGTCGA[A/G]GCTGGTTTGATCTTC | 11060 |
rs546249900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796934 | AAGTTGTAGACACCA[C/T]TGTAGGACTGTCACC | 11060 |
rs546252215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812655 | AATTTTTAAAAATTA[C/T]TTGGCAGATTCCCCT | 11060 |
rs546259881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921671 | TCTTGTGTCGTGTTC[C/G]TGCTGGGACCCACTG | 11060 |
rs546262396 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767884 | ATTCTGTCACCCAGG[C/G]TGAAGTACAGTGGCA | 11060 |
rs546275437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69897871 | CGAGATCGTACCACT[A/G]CACTCTAGCCTGGGC | 11060 |
rs546281408 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874712 | TATTGAAGACTTTAC[C/T]CCCAAATTTTACATA | 11060 |
rs546355862 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810112 | GCCCTAACTGACATT[C/T]TCCTCTTCCACGGAC | 11060 |
rs546364292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69800257 | AGAGATGTGCCTCCA[C/T]TTTAATCCTGCAGAG | 11060 |
rs546366447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793436 | GACACAAAACAGGCC[A/G]TATGGGAGACAGAGT | 11060 |
rs546366464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889501 | CTTGGCCGAATGACT[C/T]AGCCTCTTGATAAGG | 11060 |
rs546367776 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908634 | GCTTCGCCATTGGGT[C/T]GGCCTCGCATGTCAT | 11060 |
rs546381199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906279 | GGGTTTTACTGTGTT[A/G]GCCAGGATGATCTTG | 11060 |
rs546382050 | snp | C/T | 0.000399281 | 0.0141238 | missense | WWP2 | GRCh38.p7 | 16:69842027 | ATTCCTTTCTAGGAT[C/T]ACAGCTGCCTTCGAG | 11060 |
rs546390007 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776450 | AGAGTACATAATAGA[C/T]GCTCAATAAATATTT | 11060 |
rs546406245 | snp | C/T | 0.000528175 | 0.0162422 | intron-variant | WWP2 | GRCh38.p7 | 16:69908711 | CTTTCTAACAGGGGC[C/T]TATGCCTTTCCACTG | 11060 |
rs546429462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822057 | TTTTTTGTAGAGACA[C/G]GGTCTCCCTTTGTTG | 11060 |
rs546433451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842342 | TTAATTTTTGTTTTT[A/G]TTTTAGATTCAGGGG | 11060 |
rs546459229 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | WWP2 | GRCh38.p7 | 16:69828825 | CTTCTTCCATGATCT[C/G/T]ATCTCTGTTTCACCT | 11060 |
rs546462948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69927229 | GCCCCAGGGCTGTGG[C/G]TGGGGCCGGCTCCCC | 11060 |
rs546479761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69780334 | ATATTTCAGGTACTA[G/T]ATAGCATTCCATTTT | 11060 |
rs546485481 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887614 | TTTTGCCATGTTGGC[C/T]AGGTGGATCTCGAAC | 11060 |
rs546499621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881753 | CTGGAGTGCAATGGC[A/G]TGCTCTCAGCTCACT | 11060 |
rs546509057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847790 | ACATTAATTTATTCA[C/T]GAGGGATCCACCCCC | 11060 |
rs546521557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922214 | TGAATTCTCAAGCAC[A/C]TGGATTTTGTTCTGC | 11060 |
rs546586012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813148 | CCATGGGTTATAACT[C/T]ATTTCTGGTGTAATT | 11060 |
rs546588845 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69900057 | GGGGGTGTTTAGGTT[A/G]CTTCCAGTTTTTCTG | 11060 |
rs546603673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933384 | TGTTGGGGTCTGGGG[A/G]TGAAGGGAGGGCAAA | 11060 |
rs546607118 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813739 | GTCCCAAAGTGCTGT[A/G]GGATTACAGCTGTGA | 11060 |
rs546611741 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69770233 | AGGATTTGGGGGCCA[A/G]TGGCCAGGGAAACCA | 11060 |
rs546648541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900803 | TGCTGGAATTACAGG[C/T]GTGAGTCACCGTGCC | 11060 |
rs546663326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932096 | GCACTTTGGGAGGCT[A/G]AGGCAGGTGGATCAC | 11060 |
rs546679825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69911964 | CTGGAAAGCCTCAGC[A/G]ATTAGAGGCACCAAG | 11060 |
rs546680467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898798 | AACCTCTGCCTCCCA[C/G]GTTCAAGCAGTTCTC | 11060 |
rs546685202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777174 | TACACATATGGATAT[A/C]CACATATGTGTATAT | 11060 |
rs546717440 | in-del | -/AAG | 0.0158469 | 0.0875917 | intron-variant | WWP2 | GRCh38.p7 | 16:69848508 | AGGTGCAGTGGCTCA[-/AAG]TGCCTGTAATCCCAG | 11060 |
rs546723970 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69769340 | AAAAAAAAAAAAAAT[A/G]GAAGTGGGTGCAAGG | 11060 |
rs546725596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804410 | TCATTTTTTTCCCTA[A/G]TATGTAGCTGATTGG | 11060 |
rs546746274 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69922119 | AACAGATTATTTTGT[-/G]GCTCTTAGGGTGTGG | 11060 |
rs546754934 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807369 | TTAATAATGAAAACA[C/T]GTTTGCTTTGTACTT | 11060 |
rs546767982 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69918580 | CCTACTGTCTGACCC[G/T]TTGCTGAAAAAGTTT | 11060 |
rs546772274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894405 | TTTTGAAATATGCAG[C/T]AGATGAGACTTTGGC | 11060 |
rs546820099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927849 | ATTTACAAAATAGAG[A/T]TGAAGTCTCGCTGTG | 11060 |
rs546822396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69779273 | GTTATTTTTCTTTAT[A/G]CATCAATTGGAAAGG | 11060 |
rs546835557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825334 | GAGGCTGAGGCAGGA[G/T]AATCCCTTGAACCCA | 11060 |
rs546839847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792442 | AATCTCACATAAAGT[C/T]GTGACTCTGTGTATA | 11060 |
rs546868069 | in-del | -/T | 0.441158 | 0.161117 | intron-variant | WWP2 | GRCh38.p7 | 16:69862709 | GCCAGCCATGAATTC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs546871022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806291 | TTGCTCAAGATAGAC[C/T]ATTCCTTGAAAATTT | 11060 |
rs546909253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894039 | AGGAGCAAGGTTCTC[C/T]TGGGGATCTCATGGC | 11060 |
rs546914295 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787390 | GCCCAGAGTTTCAAG[A/T]CCAGCCTGGGAAACA | 11060 |
rs546914570 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859705 | GGCCCCGACCCCTGC[A/G]TTCCTTCTCACGGTG | 11060 |
rs546918663 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69911331 | TGTTCAGACCACAGG[G/T]AAGCAAAGAGTGATC | 11060 |
rs546926662 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | WWP2 | GRCh38.p7 | 16:69918884 | AGTCTTGCTCTGTTG[-/C]CCATGCTGGAGTGCA | 11060 |
rs546930642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885927 | GGTATCTGATTTATT[A/G]TGTTTAGTTCCTGAT | 11060 |
rs546935641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791345 | CAATTCTCCTGCCTC[A/G]GCCTCCAAAGAAGCT | 11060 |
rs546937239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790655 | ATCTTGGCTCACTGC[A/G]ACCTCTGTCTCCTGG | 11060 |
rs546997999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846444 | AATGGATGGGGCTGG[A/G]TGTGGTGGCTCACGC | 11060 |
rs546998268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832555 | AAAAATTTTTAATGT[A/T]TTTTGAGACAGAGTC | 11060 |
rs547000889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69871991 | TCTCACCCGTTCTAA[C/T]GTGGACACGGGATCC | 11060 |
rs547004683 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69785034 | TGAGGTTAGGAGTTC[A/C/G]AGACCAGCTTGGCCA | 11060 |
rs547018951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783896 | GGAGTTCAAGGCTGC[A/G]CTGAGCATGTTCATG | 11060 |
rs547031804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936876 | GTCTGAGGTTCAGTC[A/G]GCGCTGGGGGCAGGA | 11060 |
rs547050188 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777591 | CAGGCATGAGCCACC[G/T]TGCTCGGCCTATATT | 11060 |
rs547072895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851747 | GCACTGTGGGAGGCC[A/G]AGGCAGGCATATCGC | 11060 |
rs547094730 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931617 | CCAGTGGCAGGCCGA[C/T]GCCCTCCTCCCAGCA | 11060 |
rs547140699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878670 | CCCAGCCTGTTTTTA[C/T]ACATGGTTTCATGTA | 11060 |
rs547150202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784445 | TGCCTTTTCACTGTG[A/G]TCCCATTCACACCAA | 11060 |
rs547160596 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812669 | ATTTGGCAGATTCCC[C/T]TCAACTTGGGGCTGT | 11060 |
rs547179956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767882 | TCATTCTGTCACCCA[G/T]GCTGAAGTACAGTGG | 11060 |
rs547194739 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838313 | GGTGCACAGCTCTCA[A/G]GGACTAGAACTGTGA | 11060 |
rs547195596 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69776835 | TTCCATCTCGAAAAA[A/T]AAAAAATAAAAAAAA | 11060 |
rs547223190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932706 | GCAGGGCTCAACTGC[A/G]TGTCACATGCCTGGG | 11060 |
rs547228257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874287 | CAGAAGCTCCCCTCT[C/T]CAGCAGCGCAGGACC | 11060 |
rs547255288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775301 | GTCAGAAAATCTTTC[A/G]TAGGCTTTATGACCT | 11060 |
rs547257887 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69840889 | TAACCATGGCACTTT[-/C]CAGACACCAAGCAGG | 11060 |
rs547258022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887101 | GGGGTCCTTGTGAAC[A/G]TAAGTGATCATCAAA | 11060 |
rs547264479 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923158 | GACTCCCAAAGTGCT[C/G]GGATCACCAGCCTGA | 11060 |
rs547272016 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69859482 | ATCGCTTGAGCCCAG[A/G]GAGGTCGAGGATGCA | 11060 |
rs547286348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811300 | TTTTTTCCCTCCCCA[A/G]TTTTTGTATTTTTAA | 11060 |
rs547291983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69841050 | TTGGTGCTTGGAGAA[A/G]AACATGTGTCATTCA | 11060 |
rs547293214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69904296 | CAGCCTCTTGAGCTG[A/G]CAATATTGTTACCCC | 11060 |
rs547299550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880365 | ATGATTTTTATTACT[G/T]ATGTGTTATCGTATT | 11060 |
rs547360596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822171 | CATGCCTGACCCCTG[C/T]TTTTCTTTCCTTCTT | 11060 |
rs547366393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69873342 | TCTGTGGACCACAAG[A/G]TGGAGTGGTCTGTGT | 11060 |
rs547383089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857241 | CCCGAGTAGCTGGGC[A/G]CGCTCCACCACGCTC | 11060 |
rs547409005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866135 | CCATTCAGTTGGTTG[A/C]GGAGCTTAGGATTTT | 11060 |
rs547412375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909324 | CTTTCAAAAGGGGAT[A/G]TATTCTGCTCCAAGA | 11060 |
rs547463653 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894772 | CAGTGCTCATTATCA[A/G]TGAGCCAACTGTGTG | 11060 |
rs547463722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69831595 | AAATATGACTCATCC[C/T]TGCTGCACGTACAAA | 11060 |
rs547469264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930971 | TCTAAAAGCAAGAAG[A/T]CTGGCTTTATTTCTA | 11060 |
rs547508812 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891297 | CCCTGGTGTTCCAGA[G/T]TCAGGGGACCAATGA | 11060 |
rs547530136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923645 | TACTGACTCCAAAAC[A/G]AGACCTGAAGCAGCA | 11060 |
rs547566057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850749 | TATTAGGGATGATAG[C/T]GTAGCAAACTAGGGT | 11060 |
rs547598823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905297 | TTGTCCGCTTTGGGG[C/G]GTGTGTAGAACCTCC | 11060 |
rs547602002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69870721 | TGGTATTTGAAACAT[C/T]TCACAGTTGCAAAGT | 11060 |
rs547637998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782931 | TTGCCGCAGCCTCCC[A/G]GTGTGCTGGAATTAC | 11060 |
rs547639108 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69857764 | CCTCCCAGGCTCAAG[G/T]GATCTTCCCACCTCA | 11060 |
rs547639421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849901 | GTACCTTATTATACA[C/T]TTATTTATTGCATAG | 11060 |
rs547652120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816707 | TATACACACGTATAC[A/G]TGTACACATGTACAT | 11060 |
rs547678278 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935193 | TTCTTCCCCTGCCTT[A/C]CTGAGTGTCCCACCC | 11060 |
rs547696204 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | WWP2 | GRCh38.p7 | 16:69897105 | CCGTCTTTTTTTTTT[C/T]GTTTGTGTGTTTTGT | 11060 |
rs547696924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891103 | GTCAGCCACCTACCT[A/G]GAGACTGACTAGCAC | 11060 |
rs547697213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69823570 | GCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 11060 |
rs547702055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850256 | GCCGGGCGTGGTGGT[A/G]TGCGCCTGTAGTCCC | 11060 |
rs547704385 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69858823 | TATCTCATTTATACT[A/G]GGTGTTCAAATTCCC | 11060 |
rs547716906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844895 | CATTCAGCAGGAAAT[A/G]TTTTTGCAAATATTA | 11060 |
rs547743596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765818 | GATGAAGTGAGACTC[C/T]GTCTTGCTTTTGGAG | 11060 |
rs547761379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764946 | TGGTGGCTCATGCCT[A/G]TAATTCCAGCACTTT | 11060 |
rs547767722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809281 | ACCTAACATTCCAGC[C/G]ATGTTTCATAAAGTC | 11060 |
rs547779617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902998 | GGACATTTAATCTGA[A/G]CAGGGGTCCAACTGC | 11060 |
rs547781358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808894 | TGCGTATGTACAGAT[C/G]TAGGAGCTTTGGTTC | 11060 |
rs547794213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774316 | GCTGGAGTGCAGTGG[C/T]GTGATCATAGCTCAC | 11060 |
rs547802513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799762 | TATTACAAATAGTGC[C/T]CTGTGCTTACTCGGC | 11060 |
rs547839905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896080 | GTTTTCACCTTATGT[A/G]TATGTATTCATGCAT | 11060 |
rs547841536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870124 | GAGCTTCTCTGTGTC[G/T]GTTTGCTTATCTGTA | 11060 |
rs547875386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69807075 | CTCTTTTTGCCCAGG[A/G]TGGAGTGCAATGGCA | 11060 |
rs547898250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793142 | GGGATCATGAGGTCA[A/G]GAGTTCAAGACCAGC | 11060 |
rs547910500 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856550 | GGGAGACTGAGGTGG[A/G]TGGATCACGAGGTCG | 11060 |
rs547914279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807679 | AAAGGGCAGCCAGGT[A/G]CAGTAGCTTATGTCT | 11060 |
rs547931249 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69890829 | ATCGAGCAGCCCAGG[A/G]AAGCCGATTCCCCTC | 11060 |
rs547942012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69939578 | GGGCATCTGATCTAC[C/T]GGGTTTTACATATGA | 11060 |
rs547981490 | in-del | -/ATTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790966 | GTTTCTTATTACATT[-/ATTG]ATTGTTTTTGTAGTC | 11060 |
rs547981748 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821994 | CCACCCCAGCCTCCC[A/G]AGTAGCTAAGACCAG | 11060 |
rs547988079 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69764000 | TTACTTTCCCATTTA[A/C]AAAGAGCGTATACCA | 11060 |
rs547991663 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844404 | GTGATGCCTTCTCAG[C/T]TTTGGTGCTAGTAAC | 11060 |
rs548023628 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763104 | AAGTGTGGGCACTTT[G/T]CCTGTAAAATGGCTT | 11060 |
rs548026174 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69821102 | GTTTTTTTGATTGGC[A/C]CCAGATGCCAGGCTT | 11060 |
rs548027816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829037 | ATTCTGTATTTCATC[A/C]TATAGAGCCTCTATT | 11060 |
rs548028773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802574 | CTTATTCATGTTGTA[A/G]CATGCGTCAGAAGAT | 11060 |
rs548030680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795184 | GAGGCTGCAGTGAGC[C/T]GTGATCGTGCCACTG | 11060 |
rs548033451 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941404 | GGGAGGTGCAGCCTG[C/T]GTCTGCCTCTGTCGT | 11060 |
rs548061632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914126 | AATTTGGAGATAAGA[A/T]GATGAGAAGATGTGA | 11060 |
rs548063582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69787658 | CTAGGGCTCGTTGCT[A/G]CCTGCACTCGCTCCC | 11060 |
rs548096044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935630 | CTGCCCAGTCCTTGC[A/G]GTCTGCAGGGCAGGG | 11060 |
rs548100943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896584 | TAAAATTTTTTAAAG[C/T]TTTTTTCTGATCTTA | 11060 |
rs548104687 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69800819 | ATCTGCCCGCCTCAT[C/G]CTCCCAAAGTGTTGG | 11060 |
rs548119585 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69895044 | AGGAGGGATGTTTTC[G/T]GGATCTTTCGGATTT | 11060 |
rs548191966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69889289 | ATGATCACACCACTG[C/T]ACCCCAGCCTGGACT | 11060 |
rs548200059 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830625 | ACCCTGCCAGAGTGT[A/G]AGTGTTGGGGGGCCG | 11060 |
rs548210381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843107 | ACTTGACTGCTTTTT[G/T]GTATGTCCGGGGCTG | 11060 |
rs548260221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855374 | ATTCTGCTGCAATGA[C/G]AGTCACCAAAGCCCC | 11060 |
rs548275501 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825728 | CCTCCTGGGCTCAAG[A/T]GATCCTCCCACCTCA | 11060 |
rs548286825 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853904 | ATCTCCCATGGTGGT[C/T]GGCTTTGGTGTTCAG | 11060 |
rs548292304 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940196 | TTCCAGAGGGCTGAC[C/T]CTCTCTGCAAAACTC | 11060 |
rs548313872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881697 | TTTTAAATTTTTTAA[A/T]TTTTTTATTTTTTAG | 11060 |
rs548319663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69784646 | TTGACTCCTGAGCAC[A/G]TGTTTTTAATATTCT | 11060 |
rs548323839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856270 | CAAAATTCTAGGGAC[A/G]GAAATCCAATCTGAA | 11060 |
rs548357746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771227 | TGTGTAGTTGTTTTC[C/T]CCTGTCAAAAGTTCT | 11060 |
rs548401203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901637 | ATTTTCTAATGGAGA[C/G]AGTGGATTTTGATTG | 11060 |
rs548408248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914915 | ACTCCATGATTTATC[A/G]CACCAAATCCCACCA | 11060 |
rs548410188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926809 | GAGAGAGTAAAACTC[G/T]GAAGACCCTGCGTCG | 11060 |
rs548415655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877187 | GTTTCGTGTGGCCAA[C/T]CCCGTCAATGATCTT | 11060 |
rs548431682 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69777883 | ATCAGCCTGAACAAC[A/G]TAGGGACCCCCTTCA | 11060 |
rs548473669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923179 | ACCAGCCTGAGCCAC[A/G]GCACCCGGCCGCCAT | 11060 |
rs548485297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836051 | CAGGTGATCCACCCA[C/T]CTCGGCCTCCCAAAG | 11060 |
rs548485360 | in-del | -/TTCATGTGTGT | 0.00119737 | 0.0244387 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941580 | TCAGGCTCACGGGTG[-/TTCATGTGTGT]TCGTGCGTGTGTGTG | 11060 |
rs548507290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69786703 | TGATCTGGCCATCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs548510298 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807667 | AAAAGGAAAATGAAA[C/G]GGCAGCCAGGTGCAG | 11060 |
rs548544150 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787559 | CACACCACTGCACTC[A/T]GCCTGGGCAACAGGG | 11060 |
rs548545155 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786687 | AACTCCTGACCTCAG[A/G]TGATCTGGCCATCTC | 11060 |
rs548550692 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69876637 | CCAAAGTGCTGAGAT[G/T]ATAGGCGTGAGCCAC | 11060 |
rs548563823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69860163 | TATAAAAAAAAATCA[A/G]AAAAATTAGCCAGGC | 11060 |
rs548565230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868461 | GGGCTGGAGTTGATC[A/G]TGGACATGTCTGTCT | 11060 |
rs548584279 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69785099 | AAATTAGCCAGGTGG[G/T]GCTGGTGCCTCTAAT | 11060 |
rs548587783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819640 | CTTGAACTCCTGGCC[C/G]CAAGCAATCTTCCTG | 11060 |
rs548609220 | in-del | -/CT/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831827 | GAAAAAAACAAAACC[-/CT/T]TTTTTTTTTTTTTTT | 11060 |
rs548623862 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69825788 | ATGCCACTACACCTG[-/TC]TAAGTTTTTACATTT | 11060 |
rs548631016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861490 | ATGGACTTGGCAGCG[A/G]TTTTATTTTTACCTT | 11060 |
rs548639555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887876 | GCATTAATGACTTGC[C/T]GTACTTTTCAAAGTC | 11060 |
rs548647368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770518 | GTCTCTTCATTTGTA[G/T]CCTTCATAATATCCT | 11060 |
rs548652650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926522 | TTGGAGCTGGATCTT[C/T]TCGATGCAGACACTT | 11060 |
rs548674670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817984 | GGGTCAGAAGGTGGG[C/T]GTGTTTCAAGTTTTT | 11060 |
rs548679429 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785118 | GGTGCCTCTAATTCC[A/C]GCTACCCATGAGGCT | 11060 |
rs548682836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768843 | TCTTTGTAAGGATGT[C/T]ATTTGGCAAAGTTGA | 11060 |
rs548693533 | snp | C/G/T | 3.29931e-05 | 0.00406149 | missense, stop-gained | WWP2 | GRCh38.p7 | 16:69798720 | CATAATCGTCAACCT[C/G/T]GAATTAACTCCTACG | 11060 |
rs548694313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69792216 | TCGAGGCCCTTAAAC[A/G]TAGGACAGCTATTTT | 11060 |
rs548709052 | in-del | -/TTGTT | 0.0166325 | 0.0896639 | intron-variant | WWP2 | GRCh38.p7 | 16:69862057 | AAATCAATAATCAGG[-/TTGTT]TTGTTTTGTTTTGTT | 11060 |
rs548720992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833430 | CTGGTGTGGTGATAT[C/G]TGTTTCCATCAGGAG | 11060 |
rs548727876 | snp | G/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761175 | GCAGGCACAGTGGCA[G/T]TCGCCTGTAGTCTCA | 11060 |
rs548737716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69820444 | AGATGGGATTTCACC[A/G]TGTTGGCCAGGCTGG | 11060 |
rs548754388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862052 | GGAGGAAAATCAATA[A/G]TCAGGTTGTTTTGTT | 11060 |
rs548789789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824302 | GTAGGAGGCTTATTC[A/T]TTGTGGGAGAGTGGT | 11060 |
rs548800262 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813717 | CTAGTGATCCTCCCA[C/T]GTTGGCGTCCCAAAG | 11060 |
rs548808163 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910619 | TTTCACCATTTTGGC[C/T]AGGCTGGTCTTGAAC | 11060 |
rs548819011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69852826 | ATACAGTTTTATTTT[C/T]ATATGGCCATACTCA | 11060 |
rs548832255 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920014 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 11060 |
rs548835010 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | WWP2 | GRCh38.p7 | 16:69867157 | TTTTTTTTTTTTTTT[A/T]AAACCAAACAAACAA | 11060 |
rs548846591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774365 | GGCTCAAGCGATCCT[C/G]CCACCTCACCTCAGC | 11060 |
rs548864896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913093 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 11060 |
rs548891416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869019 | TCAGCCTCTGAAGTA[A/G]CTGGGATTATAAGCG | 11060 |
rs548915527 | in-del | -/TCTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763689 | AAAACAATTTATTGC[-/TCTT]TCTTGTTTGCTGGCC | 11060 |
rs548920891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845522 | ACTTGGGTGCTATTC[A/G]CTGTGATCAAACAAA | 11060 |
rs548929126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69887251 | AGCATGAGCCTTTAC[A/C]AGAATGAGCACATTA | 11060 |
rs548933846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811241 | AGACTTTGGCTTTCC[C/T]AGAATCTCCTACTTT | 11060 |
rs548941000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841119 | GCACTAGGTCTTAGA[A/C]CAGGCCCTAGCCAGA | 11060 |
rs548957021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867702 | AGGACACACCGCATC[C/T]TGAGAAGGGCGAGCT | 11060 |
rs548962219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905597 | CAAAATCTGAAAACA[A/G]AAAATCCAAAATCTG | 11060 |
rs548963801 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910376 | TGTGTACTTTATAAC[A/G]TGTGCACTTTAAAAC | 11060 |
rs548983271 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926177 | ACTTAGGAGAGATGA[C/T]AGGCTTCATGGCTAT | 11060 |
rs549007276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812052 | CCAGGACCTCATGCA[A/G]GATGCAGTGTTTAGT | 11060 |
rs549025703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906248 | CAGCTATTTTTTTAT[A/G]TTTTTAGTAGAGACA | 11060 |
rs549056138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776019 | CTTAAATAGAGTGTA[C/T]GCCTTTCAGCCCTAA | 11060 |
rs549063128 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69897675 | AGCACTTTGGGAGGC[C/T]GAGCTGGGTGGATCA | 11060 |
rs549064985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904770 | GCAGTGGGAGGAACC[A/C]GGGCATCTGGGTCAA | 11060 |
rs549085728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851591 | CATTCCTCCTCCACA[G/T]TTTATTCATTCATTT | 11060 |
rs549088105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906423 | GATCAATGCAGTCCA[C/T]TAACCAGACATCCCA | 11060 |
rs549090622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860463 | TTAGGATGTTATGAG[A/G]GAATGAAAGGAAATT | 11060 |
rs549099998 | snp | A/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69936810 | TGTGCCCGTTCTCCG[A/T]GCCTGTTCCTCAGGC | 11060 |
rs549144779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925545 | CGGTGCTCTGTCCTC[C/T]CCTCCCGCGTGTCTT | 11060 |
rs549150959 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813574 | TTCAAGCGATCCCCC[A/C]ACCTCAGCCTCCAGA | 11060 |
rs549182116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766726 | TTTACTCAACCATCA[C/T]CTTCAGAGAGAGGCT | 11060 |
rs549228074 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69795244 | ATGGTTTTACCTAGG[-/A]AAAAAAAATGCGGAT | 11060 |
rs549256143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69812548 | CAGTGGTGTGAACAC[A/G]GCTCACTGCAGCCTC | 11060 |
rs549266341 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762038 | CTCAATTAAGTATTT[A/G]CTGACTTAACAGTCT | 11060 |
rs549281658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932067 | AGGCGCGGTGGCTCA[C/T]GCCTATAATCCCAGC | 11060 |
rs549288695 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926067 | CTAGTTATTATCGCC[A/G]TGTAGATTTCTCCTC | 11060 |
rs549289663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839429 | TAGCCTGCCTAGGGC[C/T]TGGTGCTTCTGCCTC | 11060 |
rs549295333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804578 | CACTCTGTCTATGCT[A/G]TTGTAAAATTATGTT | 11060 |
rs549298173 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772512 | GAGGCAGCAGAGTTA[C/T]AGCTCCGTGACTGCT | 11060 |
rs549309270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891266 | GAGATCCAGGCAAGG[C/T]GGGTTATTAATTTAC | 11060 |
rs549330415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902113 | GAATGGTTGAACACA[C/T]ACTGTAACAACGGGT | 11060 |
rs549331946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805288 | CGATTTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 11060 |
rs549335923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844996 | GTGCACACATGCTTA[C/T]GACTGTAGGCGGTGG | 11060 |
rs549345522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839896 | TGCTGACCCAGTGAT[A/G]TGAAATGTTTAGAAA | 11060 |
rs549456405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897514 | TCCCTGTATACAGTG[A/T]TACATGGAACTTGGG | 11060 |
rs549480273 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781550 | GATGGAGTTTGACCA[C/T]GTTGCCCAGGCTGGT | 11060 |
rs549481617 | in-del | -/TTTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817674 | CTTTTTTTTTTTTTT[-/TTTTTTTTTTTT]AAAGAGATGGAGTCT | 11060 |
rs549493817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788008 | CCTGTCCTGTCTCTC[C/G]GCTTCTGCACTTTGC | 11060 |
rs549515763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840058 | GAAATGAAAGCTTCT[A/G]ATTTAGAGAATCTTA | 11060 |
rs549531760 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69917238 | ACCAAGGAATTGGCT[G/T]TTCTCCCATTTTTCT | 11060 |
rs549556407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872650 | AGTATTGTTGCTAAG[A/G]GCTGAGTCAGATGAT | 11060 |
rs549601800 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904075 | CCATTGGCGCTCAGC[A/C/G]CTTTCATTTTTTAAT | 11060 |
rs549603387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823766 | AGCCACCGTGCCCAG[C/G]CAAAAATTTTTGTTA | 11060 |
rs549619037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783258 | CAAGTGATCTGCCTG[C/T]GTTGGCCTCCCAAAG | 11060 |
rs549624218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781657 | TTACTCTGAGTTAGA[C/T]GGTGTCTTAGTTCAT | 11060 |
rs549639420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795067 | GGTGAAATCCCGTCT[C/T]TACAAAAAAAATTAA | 11060 |
rs549656087 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886682 | TGAGAATTGCTTAAA[C/T]CTGGGAGGCAGAGGT | 11060 |
rs549696289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775192 | TTCAGATTCTTCTCT[A/G]TGTCCTTTTGTTTTC | 11060 |
rs549712260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782152 | GCTGGGCGTGTTAGC[A/G]GGTGCCTGTAATCCC | 11060 |
rs549717492 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862848 | CTCCCACCTCAGCCT[C/T]CCGCATAGCTGGGAT | 11060 |
rs549729931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69922637 | AGAGGAGGGGCAGCC[A/G]GTTGGCTCATTGGAG | 11060 |
rs549737371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886277 | GTAGAGATGAGTCCT[C/T]GCTAGGTTGCCCAGG | 11060 |
rs549759901 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837573 | CAGTGTGACTGTCAC[A/G]GGGGTAGAAATTAGC | 11060 |
rs549774681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878526 | TTCACTTCATTTTTC[G/T]TTTTTAAAATTTTCT | 11060 |
rs549806057 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917505 | CAGAACCACATGGAT[-/C]CCCCAAATTAGAAAT | 11060 |
rs549838636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794571 | TTTCTCCCAAAATTA[A/G]CTTGGCCCATGCCCA | 11060 |
rs549855901 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868916 | GTTGAGACAGAGTCT[C/T]TCTCTGTGTTGTCCA | 11060 |
rs549857296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935570 | CAGCCGGCCAGCGTG[C/T]GGGGCAGATGCGGGC | 11060 |
rs549887861 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769949 | GCATAATCTCGGCTC[A/G]CTGCAGCCTCTAAGC | 11060 |
rs549897846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829118 | CCTCTTGCCCACCCC[A/G]TTTTCTAATCTCTTT | 11060 |
rs549909243 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930465 | CCTGGACAACATAGC[A/G]AGACCGTGTCTCCAC | 11060 |
rs549930424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766055 | TCTAGATCTAATTGC[C/T]CACAATATCTTCACG | 11060 |
rs549944213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902494 | TGTTACTCATTGAAG[A/G]CCAAGGAGCAATGTG | 11060 |
rs549946153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821547 | AGGTGTCGGCTTTGG[A/C]AGTCGGTCAGCCTCG | 11060 |
rs549961433 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867539 | TGGAGGCCAGGGCTT[G/T]GACCATCAAAGCTTA | 11060 |
rs549968583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779001 | GTTGCCCAGGCTGGA[A/G]TGCAATGGTGCAATC | 11060 |
rs549987950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865527 | GGGGGGGTACCATAA[C/G]CTGCAGGCAGGAAGT | 11060 |
rs550004825 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939967 | CCTCCCACGCCCCCC[A/G]GCGCACATGTAGTCC | 11060 |
rs550014606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69863499 | CAAAAATTAGCTGGG[C/T]GAGGTGGCAGGCGCC | 11060 |
rs550022321 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP2 | GRCh38.p7 | 16:69894220 | AGCTGGGACTACAGG[C/T]GCATGCCACTATACC | 11060 |
rs550033956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822324 | ATCAGCTTTCGTGCA[A/G]TAAGCACCTTTGAAT | 11060 |
rs550077968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857192 | CATTGCAACCTCTGC[C/T]TCTGGGGTTCAAGCG | 11060 |
rs550090075 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850672 | AGTGAAGGCAAGGAG[A/G]AGTAAGAGAACTTGA | 11060 |
rs550091565 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875939 | GGTGAGTCCTTTTTA[G/T]TTTTTATTTATTTTT | 11060 |
rs550100284 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941339 | ACTGGTCCCGGGTGC[A/C]TTCCAAGCACAGTCT | 11060 |
rs550101299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821038 | CCGCCAAATGCAAGC[C/T]GTTGTTTCATTTTGC | 11060 |
rs550119164 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788973 | AAAATTGTGTCTCTT[A/G]GGAATATTTTTCTTG | 11060 |
rs550123258 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813681 | CCATGTTGCCCAAGG[C/G]TGGTCTTAAACTTTT | 11060 |
rs550128920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69896498 | TGTACCCAGCATACA[A/G]CTTGGCTTCCAAAGA | 11060 |
rs550129252 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836025 | CCAGGCTGATCTCGA[A/T]CTCCTGGGCTCAGGT | 11060 |
rs550135918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69772545 | TGCAGAGCAGGGCTA[C/T]GCTATAGGCAGTGTG | 11060 |
rs550155708 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939523 | TCTGGCAGCTTTTGC[A/C/G]TGGCCCTGGGGTGTT | 11060 |
rs550161953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807037 | ATTTATCTTTGTCTT[C/T]TTTTTTTTGAGATGG | 11060 |
rs550171142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907875 | AGATACTCTGTAAAT[G/T]AATCTTATATTACAA | 11060 |
rs550173186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914595 | AGACACTATCTCTTA[A/G]AAAAACAAAAAATTG | 11060 |
rs550180471 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815720 | TGAACCTGAGAGGCG[C/G]AGGTTGCAGTGAGCC | 11060 |
rs550181956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773180 | CCTACCGATACACGT[C/T]GCTCCTTTTTTTTTT | 11060 |
rs550216885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69764667 | ATTCAGTGAATATTT[A/G]TAAGTACCCACTCTG | 11060 |
rs550217549 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69876492 | GCCTCAGCCTCCAAA[A/G]TAGCTGGGATTACAG | 11060 |
rs550238564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814464 | TTTATAAATATTTAC[A/G]AATTCCTTCACATCT | 11060 |
rs550256189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907100 | GTTTGCTTGTGGAAG[C/T]AGGTGTCAGAAGTTG | 11060 |
rs550259111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69786639 | ATTTTTTAGTAGAGA[C/G]GGGGTTTTGCCATGT | 11060 |
rs550274070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806348 | TATTGGGGTTTTCCA[C/T]CTATATTCGTTAGTG | 11060 |
rs550282183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847886 | CATGAATTTTGGTGG[A/G]GACAAACTGCATCCA | 11060 |
rs550309448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69914030 | TGAACTGAGATCACA[C/T]CATTGCACTCCAGCC | 11060 |
rs550310199 | snp | C/T | 4.9836e-05 | 0.00499154 | intron-variant | WWP2 | GRCh38.p7 | 16:69798851 | GAAAGCCCCTTCTTT[C/T]TGAACGCAGCAAGAT | 11060 |
rs550345883 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929411 | ACCGGCTCTCCGTGT[C/T]TGAATCTGATGTTCT | 11060 |
rs550347908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69843019 | CAGGATTCTTAGAAG[A/G]GTCAGAGGCTCCTTG | 11060 |
rs550349777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69835149 | GATTTTGAGCAATGC[C/T]TCCAAAGGCAGCAGG | 11060 |
rs550355589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69800697 | AGCCTCCCAAGTAGC[C/T]GGGATTACAGGCATG | 11060 |
rs550364998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808822 | GCCATCATGAACAAC[A/G]CTGACATAAACACTC | 11060 |
rs550370957 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768233 | AAATCTTTTTAGAAG[G/T]TTGCAGTTCCCTGTT | 11060 |
rs550388315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843951 | TTTTAGCCAATACCC[A/G]CAGCATCTTAAAAGA | 11060 |
rs550402118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900843 | TTGCCAACCTCTATT[A/G]AGGAGCTTTGGTAAA | 11060 |
rs550419296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933863 | CGACTCCCTGGGACA[C/T]GTGTCCCCATACTAA | 11060 |
rs550423193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764149 | GGACTCAAGCCCAGA[C/T]CCTTAATCCTTAGAT | 11060 |
rs550445758 | in-del | -/GGC | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69822292 | TTGTAGCAGGGGCAG[-/GGC]GGCCTGACGCTGATT | 11060 |
rs550447481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902971 | AGGTCATGGATCAGG[C/G]AGGACCCGCAGGGAC | 11060 |
rs550472096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815256 | GATCAGGCCATCTTG[A/G]CCTCCCAAAGTGCTG | 11060 |
rs550474370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807941 | AGCCTGGGTGACAGA[A/G]CAAAACCCTATCTCA | 11060 |
rs550485918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920388 | TGACATCCAATTCTG[A/G]CATGTTTCAGAATTG | 11060 |
rs550506495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876022 | TGCAGTGGCATGATC[A/T]CAGCTCACTGCTGCA | 11060 |
rs550509362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901537 | CCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 11060 |
rs550516518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69793494 | CTCAGAGATTAGGGT[G/T]TTTATAGACAATTTG | 11060 |
rs550517793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808039 | CGTAATCATCACCCA[C/T]ATCAAGACATAGCAT | 11060 |
rs550548473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855134 | TTACAGGCATGAGCC[A/G]CTGAGCCCCAGCCGG | 11060 |
rs550572645 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894445 | TTACACACGTCTGCA[A/C/T]GTTTTAAGAACTGAA | 11060 |
rs550575242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791489 | CACCTCGGCCTGCCA[A/G]AGTGCTGGGATTACA | 11060 |
rs550581858 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810785 | TTTGAGACGGAGTCT[C/T]GCTCTGTTGCCCAGA | 11060 |
rs550584764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763262 | TTTCCCTTAGCTTAT[C/T]TTGTGACTGCTTATC | 11060 |
rs550621088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927918 | CCTCCTGCCTCAGCC[G/T]CCCAAAGTGCTGGGA | 11060 |
rs550631503 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69918136 | TTCCCCGTCTTTCTT[-/C]CGAGATCGGCTTTCA | 11060 |
rs550640777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893243 | ACTCTTCTCACACCT[G/T]TCATTGCTTGTTTTC | 11060 |
rs550656277 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833518 | AAGGGCACAGTCCCT[A/G]GGGACTTCCCAGAGT | 11060 |
rs550676804 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929376 | CAGCACCCAGGAGGT[A/G]GGAACCTCAGGGAAA | 11060 |
rs550681671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926472 | GGAAGTTGGCAGTGA[A/T]AGGATGGGCATCTGA | 11060 |
rs550688775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69790795 | TGGCCAGGCTGGTCT[C/T]GAACTTCTGACCTCA | 11060 |
rs550701217 | snp | A/C | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69774744 | GGAGGCCAAGGCAGG[A/C]GGATGGCTTGAGCCT | 11060 |
rs550705026 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69762687 | GGAGAGGAGCTTAGG[G/T]TCCCAGGCATGGAGA | 11060 |
rs550735441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928731 | CCAGGACAACATAGC[A/G]AGACCCTGTCTTTAT | 11060 |
rs550736864 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912019 | CCTTGGCTGGGCTCG[A/C/G]TTGCTCACGCCTGTA | 11060 |
rs550787276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69797616 | TAAATTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 11060 |
rs550798454 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920976 | TAGCAACATTATTCT[C/G]GGTTTATAGAGGTAG | 11060 |
rs550799190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882738 | AAGTAGTGAAAAATG[C/T]GGGAAACAAATCTGC | 11060 |
rs550800517 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906786 | TTGGGAGGCTGAGGC[A/C]GGGGTATCACTTGAA | 11060 |
rs550812973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848334 | GCATGCCTGTAATCC[C/T]GGCTACGTGGGGAGC | 11060 |
rs550841943 | snp | A/G | 8.24436e-05 | 0.00641989 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799243 | GAGAAATGAACTGCT[A/G]GGCACCGCATCTGTC | 11060 |
rs550872423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888500 | AGCTTGACTCAAAGA[A/G]TGTGGCTTTTACGGA | 11060 |
rs550883776 | in-del | -/TTGAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925777 | TATTGGCTTTTGGTC[-/TTGAG]TTTCAAGGTGTCTAC | 11060 |
rs550894418 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834583 | CCCAGGCTGTGTGCA[A/G]TGGTGCAATCTCGGC | 11060 |
rs550923070 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838675 | GGGTTGAAAGGCCTC[A/G]GTTCCTTCCCATACT | 11060 |
rs550929757 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818918 | AGCTAGGGCTTCTCC[C/T]CTGGCAACCAAAGAC | 11060 |
rs550935673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889135 | CCTGGGCAATATAGT[A/G]ATATCCTGCCTACAC | 11060 |
rs550982868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841081 | CTCATTCAACACATA[A/T]ATATGTAATTGTATT | 11060 |
rs550997669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926930 | ATTTCAGGCTCTGTA[A/G]AGGCAGGTGATGTAG | 11060 |
rs551001454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923746 | CAAGGTCACTGCTGT[A/G]GCTCAGCACTTACCC | 11060 |
rs551004082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69825576 | TTATTTTGAAAGCTA[A/G]TATTATTTATTGTAA | 11060 |
rs551032288 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801276 | TCACTTTGTCACTCA[G/T]GCTGGAGTGCAGTGG | 11060 |
rs551038988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777296 | CTTTGTGTGTGATAT[A/G]CTTTTATATTTTCTT | 11060 |
rs551044304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69805186 | CTGGGATTACAGGCG[C/T]CCAACACCATGCCTA | 11060 |
rs551051994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932243 | CTGAGGCGGGAGAAT[C/T]GCTTGAACCTGGGAG | 11060 |
rs551053948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938471 | AACAATATAAAAAAT[A/T]AGCCAGGCATGGTGG | 11060 |
rs551056157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846542 | CCTGGCCAACATGGC[A/G]AAACTTCTTCTCTAC | 11060 |
rs551067239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775996 | TTGGTTTTCCCTAAA[A/T]ACTCCTTCTTAAATA | 11060 |
rs551077059 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69847107 | TTTTTAAATTTGAGA[C/T]GGAGTCTTGCTCTGT | 11060 |
rs551110724 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69816551 | TAAAAAGTAAAAAAA[A/G]CAATACAGGCTCATA | 11060 |
rs551140557 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777761 | TATTTATATTATATA[A/T]AAATATGTTATTTAT | 11060 |
rs551196147 | in-del | -/CAAAAAAAAAAAAAAAAAAAAAAAAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912923 | CCAGTCTCTACAAAA[-/CAAAAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAATATATATAT | 11060 |
rs551223521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881597 | GTATTATTAAGGGAA[A/G]CTGGGTGAAGACCAT | 11060 |
rs551234226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867096 | CTGCCTCAGCCTCCT[G/T]AAGTGCTGGGATTAT | 11060 |
rs551253187 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925958 | TTGACTAATAGAAGC[C/T]ACCTTTTTATTTCTG | 11060 |
rs551264872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768779 | TTCCACGGGGCTTCC[A/G]ATAGTGTACCTCCCT | 11060 |
rs551264900 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760376 | CTCTGTCGCCCAGGC[C/T]GGAGTGCAGAGGCGT | 11060 |
rs551277832 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69800172 | TTGAGCCTCCTCTGG[-/T]TCTTTTCTTTTCGGC | 11060 |
rs551286334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804520 | ATTTGGGCCTGCTTA[A/G]GGACTTTCCATTGAA | 11060 |
rs551297359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859997 | TTGGAGGGGGGCTAG[A/G]GTGAGAGGGATGTCA | 11060 |
rs551322634 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867816 | TTTCTGCCTGCCCTG[A/G/T]GGGCTGTATAACTCG | 11060 |
rs551337388 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892116 | GCACCTAGCCTGGCA[C/T]ATAGTGGGACTCCAG | 11060 |
rs551399265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824153 | CGTCCATTCCAGCCT[C/T]CCAGGTTCTCCCAGG | 11060 |
rs551437886 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819858 | TGTGCCCATTTATAG[C/T]GAATTCCCCTTTCCA | 11060 |
rs551440580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816109 | GCTAACCCAGTCCTG[C/T]ATACCCAGTTAGTTT | 11060 |
rs551443699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69904000 | TCTTCGGGAGTGCTG[A/G]AGAGTTCTCAGCTAC | 11060 |
rs551444919 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912767 | CGAATGAACACAGCT[A/G]GGCACGGTGGCTCAC | 11060 |
rs551458716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909118 | CGTACCCTATGCCCA[G/T]CCTGTCCCTAAAGGC | 11060 |
rs551488313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810348 | TTGCCCAAAAGTGCT[G/T]GTTTGCCTCTTAAAG | 11060 |
rs551492317 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941453 | CTTAGCTTGCCACAG[C/T]GCAGCCTCTTCTGTC | 11060 |
rs551507841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917154 | GAAGGGAATGTATTG[A/G]CTCATGTAACTGAAA | 11060 |
rs551545581 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69845614 | TCTTTCCTCTGCTTG[A/G]TAAAGCTGTAGAACT | 11060 |
rs551549503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774385 | CTCACCTCAGCCTCC[C/T]GAGTAACTGTGACTA | 11060 |
rs551580477 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870369 | ACAGTGACGTGATCT[C/T]GGCTCCCTGAAACCT | 11060 |
rs551588473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839321 | CTGAAGGGAACTGAA[A/G]TATTCAGTGTGGACT | 11060 |
rs551599811 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887100 | TGGGGTCCTTGTGAA[C/T]GTAAGTGATCATCAA | 11060 |
rs551616659 | snp | G/T | 9.88631e-05 | 0.00703006 | missense | WWP2 | GRCh38.p7 | 16:69936334 | AACCTGGAAGAATGT[G/T]GCCTGGAGCTGTACT | 11060 |
rs551658167 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806699 | TTATTAGAATAAGGG[G/T]TTTAAATATCATTCT | 11060 |
rs551668579 | snp | A/G | 3.37764e-05 | 0.00410938 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931477 | GACCACTTGAGGCTC[A/G]ATTTAAAGTTCTTTT | 11060 |
rs551677798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936787 | GTGCCTAGACCCACC[A/G]TCTCACGTGTGCCCG | 11060 |
rs551681221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817927 | TACCTTTATGCTCCT[C/T]TTTTTTTTTCCCTAC | 11060 |
rs551736499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924599 | AGGGGGTGTGGGGGG[A/G]ATTCTAATGTAAACA | 11060 |
rs551750127 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP2 | GRCh38.p7 | 16:69850280 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11060 |
rs551753535 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871984 | TGTGGGCTCTCACCC[A/G]TTCTAACGTGGACAC | 11060 |
rs551754470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801953 | TTTTTTTTCTGAGAC[A/G]GAGTCTTGCCCTGTT | 11060 |
rs551764119 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898171 | TAGCTGGGATTACAG[A/G]CATCTACCACCATGC | 11060 |
rs551777084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802658 | CAGGCTGGAGTGCAG[A/T]GGCGCGATCTCGGCT | 11060 |
rs551780373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794443 | CTGAGGTGGGAAGAT[C/T]GCTTGAGCCCCAGAG | 11060 |
rs551780737 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889803 | TGGTGATCTGGTTGA[C/T]GATGACTTGGTGGTG | 11060 |
rs551804723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921848 | GGAGGCTGAGGCAGG[C/T]GGATCACTTGAGGTC | 11060 |
rs551880290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864477 | GCTGTGTTCCCGCCA[G/T]CAATGTATGAGAGTT | 11060 |
rs551890136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793828 | TTATTAGAATTCAAG[C/G]CCCTCCCATAATCCT | 11060 |
rs551905148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765904 | TTGGCCTCAAGACAT[C/T]CTCCTGCCTCAGCCT | 11060 |
rs551924734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915434 | CAAGAAATAATGAGC[A/C]AGGCTTGGTGGTGCA | 11060 |
rs551932665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923827 | TTTGCCTCTGTTGCC[A/G]AATGTTTTTAATGTG | 11060 |
rs551994423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822278 | GATCATGAGCCTTGC[A/T]TGTAGCAGGGGCAGG | 11060 |
rs552014834 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69787945 | ACCCCTAGGTCCCAG[C/T]CTAGTCCAGGCCACC | 11060 |
rs552017292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789293 | GGAGTGCAGTGGTGC[A/G]ATCTCGACTCACTGT | 11060 |
rs552021866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800651 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 11060 |
rs552023532 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69885752 | TGAGCTATAGTTTCC[G/T]TAAGTGTTAAGTGGG | 11060 |
rs552063145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781428 | TTGGCTCACTGCAGC[C/T]TTGACCTCCTGGGCT | 11060 |
rs552064128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922551 | CTGCAGAGTCCCGCT[G/T]TCCCCCATCTCCATC | 11060 |
rs552084647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891184 | GCCAGAGAGAGTACT[A/G]TTTCTGCCAGCGATC | 11060 |
rs552161300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876440 | CATGATCTTGGCTCA[C/G]TATAACCTACACCTC | 11060 |
rs552170104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883563 | AAGGTATAGCACAAA[C/G]TTTCTTTTTTTCAAC | 11060 |
rs552180286 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836945 | TTTACTTTTTTGAGA[C/T]GCAGTCTCATTTTGG | 11060 |
rs552204175 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837472 | GAGTAGATAAACCAG[A/G]TAGAAGAGCTAACTT | 11060 |
rs552253621 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69850257 | CCGGGCGTGGTGGTG[G/T]GCGCCTGTAGTCCCA | 11060 |
rs552253718 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822781 | GATCAGTGCTGTCCA[A/G]TAGAAACAGAATTTG | 11060 |
rs552260698 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69849222 | GGAAGCAGAGCTAGC[A/G]GGGAGGAGGGGTGGA | 11060 |
rs552262549 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940679 | CGCTGCTGTCACTTT[C/G]TGTCCAGGAGCTGGC | 11060 |
rs552324112 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773610 | CTCAGCCTCCTGAGT[A/T]GCTGGGACTACAGGC | 11060 |
rs552329158 | snp | C/T | | | missense | WWP2 | GRCh38.p7 | 16:69917771 | ACAATACTCGGACCA[C/T]CACCTGGCAGCGTCC | 11060 |
rs552338537 | in-del | -/A | 0.394904 | 0.203722 | intron-variant | WWP2 | GRCh38.p7 | 16:69825424 | CGAGATTCCATCTCC[-/A]AAAAAAAAAAAACCC | 11060 |
rs552345590 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69764114 | CCTTACTTTAGATTT[C/G]AGAGCTAGTAAATGA | 11060 |
rs552407518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870894 | GTTCTCTGAAGATGT[A/C]TGATAGGTTTTCTGC | 11060 |
rs552441202 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773175 | CTGTTCCTACCGATA[C/T]ACGTTGCTCCTTTTT | 11060 |
rs552452248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763401 | ATCTTCCTGTTTCTC[A/G]TGTTTACTAAAATTT | 11060 |
rs552455556 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791810 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCCCCACC | 11060 |
rs552497898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827445 | CCATGTTGTTGTATA[C/T]GCTTTATAATCACTA | 11060 |
rs552527180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902884 | CTGAATGAAGGGGAG[A/G]GATTTGTGTGAATTA | 11060 |
rs552546173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846647 | AATCACTTGAACCCC[C/T]GAGGTGGAGGTTGCA | 11060 |
rs552548249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938600 | TGCAGTGAGCTGGAC[C/T]GTGCCACTGCACTCC | 11060 |
rs552550957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870200 | AATGAGAACATATAT[G/T]TAAATGCATAGCACA | 11060 |
rs552559937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779622 | CATTCTCTAAGAGTC[A/G]GGACCAAAGGCTCAA | 11060 |
rs552624281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852123 | CAAAACGGCTGCACC[A/G]GTTTGCATTGCCACC | 11060 |
rs552644025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820521 | AGTGTTGGGATTACA[G/T]GCGTGAGCCACCGCT | 11060 |
rs552648801 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808318 | TATATTGCCCAGGCT[G/T]GTCTCAAGTGATCCT | 11060 |
rs552685719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846257 | TCACAGTAAAAATGG[A/G]TGAAAAATGGTTATA | 11060 |
rs552692390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932382 | CCATGTGGCCAGTCC[A/G]TTGGGCCTGGAACAG | 11060 |
rs552715201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920321 | GTCTAGCCCAGTGCG[C/G]TCTGCACACTTTCTT | 11060 |
rs552721717 | in-del | -/A | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837651 | CCTCCAGGAAGGAGG[-/A]AAAAAAAGTGCCAAC | 11060 |
rs552727021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886737 | TCCACTCCAGCTTGG[G/T]TGACGGAGCGAGACT | 11060 |
rs552747331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69807896 | TCTGGGAGATAGAGG[C/T]TGCAGTAAGCTGTAA | 11060 |
rs552755873 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760641 | AGCCTCCACGCCCCA[C/G]CAGCCAATTTAATTT | 11060 |
rs552760216 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767036 | GGAATAGGGGTTTTG[-/T]TTTTTTTTTTTTTTA | 11060 |
rs552769317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874593 | GGCAGCCCGTCTGTA[G/T]AAATATTATATTTCT | 11060 |
rs552776615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814306 | GCTGGAACTACAGGC[A/T]TGCGGTCCTGTGCCT | 11060 |
rs552800907 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780404 | TTTAAGTTGTTTATA[A/G]TTTTTTACTATTACA | 11060 |
rs552816551 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797292 | TGGCAAAAATATTCA[A/C]CCTTGCTGGTAATCG | 11060 |
rs552825927 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782945 | CAGTGTGCTGGAATT[A/C]CAGATGTGAGCCACT | 11060 |
rs552875518 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770159 | GAGCCACCACACCTG[A/G]TCAGTGTCTTTTTGT | 11060 |
rs552881200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813887 | GTCCCAACATAATCC[A/G]ATATAGGTAAAATTT | 11060 |
rs552883111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820993 | CGTGCTGCCCACTCC[A/G]GCGAGGCTATGGGCT | 11060 |
rs552893487 | in-del | -/TAGCCTTGCCGCCTTCAA | 0.00199481 | 0.0315187 | cds-indel | WWP2 | GRCh38.p7 | 16:69940887 | CCCGAGCGCCACTCC[-/TAGCCTTGCCGCCTTCAA]TAGAGAAGAAATCCC | 11060 |
rs552906125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804654 | GCTTCTTTTCTTTGC[A/G]TATATCACATCACTA | 11060 |
rs552933270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925086 | CGGAGGCACTGGGCC[A/G]AGCCTGCTTCCCGGG | 11060 |
rs552958291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840651 | GGTTGGGAAGGGTAC[A/G]CTGTGTTCTTCTAGA | 11060 |
rs552988667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880659 | CACTCATCCCATGCC[A/G]TGCTAATTACGAAAT | 11060 |
rs553036364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69893537 | AAATATGCATCTCTC[A/G]TAGTTCAGAATGCTG | 11060 |
rs553038853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761409 | GGAACCCTGTCTCTA[C/T]TAAAAATGCAAAAAT | 11060 |
rs553085033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831254 | CTGAATTAGGAACCA[A/G]AAGAAAACAGAACTA | 11060 |
rs553091911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881084 | CAGAGGGAACCTTGT[A/G]AAATACCCAAGGTTA | 11060 |
rs553101748 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69916961 | TTGAGTCCAGGAGTT[C/G]GAGACCAGTCTGGGC | 11060 |
rs553104672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817518 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGTGTGA | 11060 |
rs553107219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782494 | AAAGGGTGATCAGTT[G/T]TGTCAGATGCTGCCA | 11060 |
rs553122900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833569 | TTCAGCCTTACTGCT[C/G]TCTGTCGACCTCCAT | 11060 |
rs553134886 | snp | C/G/T | 1.65272e-05 | 0.0028746 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937163 | CGTGGAAGAGCAGAC[C/G/T]AAAGCCTTCCTGGAT | 11060 |
rs553179966 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887669 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGT | 11060 |
rs553184698 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834060 | TTGTGTACCTCAGCC[C/T]TTCTCCTGTAGCCAG | 11060 |
rs553189861 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69919074 | GTCTTGAACTCCTGA[C/T]CTCAAGTGACCTGCC | 11060 |
rs553226803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887421 | TTTTTTTTGAGACAC[A/G]ATTTTGCTGTCAGGC | 11060 |
rs553227060 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869395 | AAAAACTTAATTTTT[-/C]TTTTTTTGTTAAACA | 11060 |
rs553227775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69789386 | AGGCGTGTGCCACCG[C/T]GCCTGGCTACTTTTT | 11060 |
rs553234718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825992 | GTAGAAGCAGCCAGG[C/T]GCGGTGGCTCATGCC | 11060 |
rs553252831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919720 | CGAAGGTTGGGATCT[A/G]CAGCAGAACTAACAC | 11060 |
rs553265318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926047 | ACTCTGGAAACGCAT[C/T]GCTGCTAGTTATTAT | 11060 |
rs553268326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823847 | TTAGTGTAGGGTTAT[A/G]TTTGTACAGTTCTAG | 11060 |
rs553301802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859780 | TGATTTGAATCTCTC[G/T]GATTTTCTCTCCTGC | 11060 |
rs553316705 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877381 | AATTGAAGAGGGTTC[A/G]GGTCTTGCTCCAGAT | 11060 |
rs553325037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839513 | TGGTATCCTTGGGGA[C/T]GGGGTGCTCTGGGCC | 11060 |
rs553331866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903133 | GAGCTTTGCGGGACA[A/G]TAATAGTCCCTGAAA | 11060 |
rs553332032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811577 | TTGTAGTGAGACACA[C/G]TCTCTACAAAAATAA | 11060 |
rs553339096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791746 | GCTGGTTTCAAACTC[C/T]TGGACTCAAGCAGTT | 11060 |
rs553350445 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855385 | TGACAGTCACCAAAG[-/C]CCCCCCTGACCTGTC | 11060 |
rs553358976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878992 | AGCCTTGTAAATATC[A/G]GTTTATAATTTTTTG | 11060 |
rs553379393 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901765 | TTTGACCATTTTGGT[A/G]TATCAATTTATAAGG | 11060 |
rs553389856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890662 | CCGGCCTCACTCCTG[C/T]GTCAGTCACAGGCAA | 11060 |
rs553414510 | in-del | -/TGCTGGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782935 | CGCAGCCTCCCAGTG[-/TGCTGGA]ATTACAGATGTGAGC | 11060 |
rs553422345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879573 | CTTTTTAAGGCTGAA[C/T]AATATTCCGTTGTAT | 11060 |
rs553431303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788807 | AACTACCCCAGCCAG[C/T]AGAACAGTGCCTGAC | 11060 |
rs553438122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870452 | ACTACAGGCATGCAC[C/T]GGTAGTGCAGCTAGT | 11060 |
rs553439073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69866680 | TACTCATATGTATGC[A/G]TATACCATACTTTAT | 11060 |
rs553460997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845081 | GAATCCTGGCCTGTC[A/G]TTTACTTGCTATATG | 11060 |
rs553467561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909014 | TTAATATTGCTCCCA[C/T]GTCTTAGGACATATT | 11060 |
rs553469086 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923975 | TCAGTAATGATTCAA[C/T]GTGATTTGTGATGGA | 11060 |
rs553499492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69871238 | GCAATGAGCTATGAT[C/T]GTGCCACTCCAGCCT | 11060 |
rs553511093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910681 | CCCAAAGTGCTGGGA[C/T]TACAGATGTGAGCCA | 11060 |
rs553537691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867256 | GAGGTAACACTGTCA[C/G]GTGGTCAGCCAGGCT | 11060 |
rs553541188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781105 | AGTTTGTATACAACC[C/T]CTGAATGCTAAATTT | 11060 |
rs553562676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69795557 | ATAGAACAGAAAGCA[A/G]ATGTGGCAAAATGAT | 11060 |
rs553562766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802865 | CCACCTTGGCCTTCC[A/C]AAGTGCTGGGATTAC | 11060 |
rs553581377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768374 | AGCACTTTAGGAGGC[C/T]GAGGTGGGTAGATCA | 11060 |
rs553587271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792499 | CTAGATAAACTTGCT[C/T]ATATCTTTATTTTAG | 11060 |
rs553602507 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69915678 | GGAGTCAGCAATGGG[G/T]CAAGAGACCATCGTT | 11060 |
rs553618057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766135 | ACACCTGCCCCTCAG[A/G]CAGCCTTCCCCATCT | 11060 |
rs553656048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775531 | GTTGCTATATCTCTC[C/T]TTACATTGCCCATCT | 11060 |
rs553684711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872727 | GTAACTACTTGGGGG[A/T]GTGCAGGGGCCATCC | 11060 |
rs553688199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815795 | CCGTCTCGAAAAAAA[A/G]AAAAAAAAGGCAATG | 11060 |
rs553717815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891299 | CTGGTGTTCCAGAGT[C/T]AGGGGACCAATGAGA | 11060 |
rs553745101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849411 | GCAGTAGCTTATGCT[G/T]AAAATCTGGGTATTG | 11060 |
rs553752749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69858066 | GAGAATGGGAGATTA[A/G]GGCCCGGTTGGTTTT | 11060 |
rs553778071 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69809111 | CTATTGCTGCTGTTG[C/G]TGGCACCAGCCGTAG | 11060 |
rs553800313 | snp | C/T | 1.84531e-05 | 0.00303747 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842082 | TCCAGAGAACCGGCA[C/T]CAGCCCCCCAGCACA | 11060 |
rs553872997 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890638 | TCCGCTGAGCGAATG[C/T]CTGGAAGGCCGGCCT | 11060 |
rs553880122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848950 | CTCACTCCTTTACTC[C/T]TCTTTTTTTGTCCTG | 11060 |
rs553882130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856519 | CGGTGGCTCACGCCT[G/T]TAATCCCAGCACTGT | 11060 |
rs553902485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890971 | TCCCCACTTGAACAT[A/G]TACGATGGTCCAGAG | 11060 |
rs553905920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876940 | GGCTTTGTTGCTCCA[C/T]TTATAAAACACAAGC | 11060 |
rs553906486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810566 | CCGAGTAGCTGGGAC[G/T]ATAGGCACCCACCAC | 11060 |
rs553925925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821971 | ACTTCTGGCTTTAAA[C/T]GATCCTCCCACCCCA | 11060 |
rs553932554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930769 | CCTAGCTACTTGGAA[A/G]GCTAAAGCGGGAGGA | 11060 |
rs553947755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862804 | GATCACAGCTCACTG[C/T]GGCCTCGACCTCCCC | 11060 |
rs553965758 | in-del | -/TCATGTATGCGTGTGTGTAG | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69813071 | AAGGGCTTTCCGTTT[-/TCATGTATGCGTGTGTGTAG]TCATGTATGCGTGTG | 11060 |
rs553978419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764221 | TTATTTTATTTTGAG[A/G]CAGGATCTTACTCTG | 11060 |
rs553978601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894789 | GAGCCAACTGTGTGT[A/G]CATGGCTTAGATAAA | 11060 |
rs554003588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69851075 | GAGTGCAGTGGCTCA[A/G]TCTCAGCTTACTGCA | 11060 |
rs554025568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69938024 | AATTAATGTGTTGAT[C/T]CTTTTATACGTATGG | 11060 |
rs554131164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928135 | AGCTCGAGTCTTGGA[A/G]TCAGGAGGGGGTTGT | 11060 |
rs554135607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934874 | GTAGAGCCCAGAGAG[A/G]GCGCGCCAGTCCATG | 11060 |
rs554137293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834419 | GTTTTTCTTCTCTAC[C/T]CCACATCCTCTCCCA | 11060 |
rs554144255 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941988 | GGCACCCTCTGCCTC[C/T]GCCTGCTGGACCCGG | 11060 |
rs554174925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895449 | TGAGCACACATGTGG[A/G]TATTACAGCAATGTC | 11060 |
rs554180979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799611 | TGATATGTTGAATGA[A/C]ACTGTCAAATACCTC | 11060 |
rs554233786 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69881604 | TAAGGGAAACTGGGT[-/G]AAGACCATACTATCT | 11060 |
rs554235278 | in-del | -/TTTCT | 0.0252325 | 0.109451 | intron-variant | WWP2 | GRCh38.p7 | 16:69791232 | TTCTTTTTTTCTTTC[-/TTTCT]TTTTTTTTTTTTTGA | 11060 |
rs554239468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798928 | TCCCTGTGGCACCTC[C/T]GACTTTTTCTACCTA | 11060 |
rs554244597 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814433 | ACTCTCATGAGAACC[C/G]TGGCACTCAACACTA | 11060 |
rs554278499 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940405 | CTGCCTGTAATTGAG[C/T]CTCTCTGATGATGGA | 11060 |
rs554302077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835308 | CACACTTACGCCTTT[C/T]AGCCTCCCCTGTATG | 11060 |
rs554337783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69933730 | AGCCGACAATCACAC[G/T]TTTTCCCAAATATCA | 11060 |
rs554348494 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796645 | TAATGCACCATTTGT[A/G]GTCCCTATTTTTTAA | 11060 |
rs554363647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791936 | ATTTTCTTACCAGGG[G/T]GGAAAGAGCCAGCTT | 11060 |
rs554387762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69829476 | TTCCAGTCCAGCCCC[A/G]TTCATCTCTGCCCAC | 11060 |
rs554397540 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69922034 | GGTGAGCTGAGATCA[G/T]GCCACTGCACTCCAG | 11060 |
rs554399639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828802 | GGAGTTTCCTATTAT[G/T]CCATCCTCTTCTTCC | 11060 |
rs554454591 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788695 | TTTTCTTATCAGCCC[G/T]TGTCCCTGTTTAATT | 11060 |
rs554467097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929198 | CCCTCCGACCAATCA[A/G]CCAAAGAAGTGCTTC | 11060 |
rs554483169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69787172 | GGAGCCAAATTTTGT[A/G]AAATAGTTTACATGT | 11060 |
rs554491199 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909109 | GCATTCCGCCGTACC[C/T]TATGCCCAGCCTGTC | 11060 |
rs554510558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907923 | AATATATATGATGCT[C/T]GGAGGAGAGGGGTAG | 11060 |
rs554522688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912521 | AGAAACAAGAGATTA[A/T]ATGCGGATGCTATCT | 11060 |
rs554523167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906118 | TGCTCTGTCGCCCAG[A/G]CTGGAGTGCAGTGGT | 11060 |
rs554564063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69777363 | TGGAGTGCAGTGGTG[C/T]GGTCTTGGCTTATTG | 11060 |
rs554566711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785695 | GCCATGGCACAGTCT[C/T]GGCCCACTGCAACCT | 11060 |
rs554582595 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69906355 | GGGATTACAGGTGTC[A/C]GCCACCGCACCCGGC | 11060 |
rs554609487 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827102 | CCTTGTGTCATTTCA[C/T]TTGTTGACACTCCTG | 11060 |
rs554623172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818326 | AATTCTCCTGCCTCA[C/G]CCTCCCAAGTAGCTG | 11060 |
rs554630425 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69875561 | TCTCAAACTTTGCTG[C/G]AGCTTTATCAACTAA | 11060 |
rs554636811 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770581 | TTCCTTGAGTCCTGT[G/T]AGTTGCTCTAGCAAA | 11060 |
rs554639101 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801992 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACCA | 11060 |
rs554645129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69769143 | CTAACGTGATGAAAC[C/T]CATCTCTACTAAAAA | 11060 |
rs554657380 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940749 | GGGTCCAAGAGTTTC[C/T]CAAACAGCCACGCCT | 11060 |
rs554713263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805587 | ATTTATTAATCATTG[C/T]AGGTTAAAAAAAAAG | 11060 |
rs554720821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69918127 | AAAACTGAATTCCCC[A/G]TCTTTCTTCCGAGAT | 11060 |
rs554725736 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874216 | GGCAGCCTGTACTTT[A/G]TATAACGTCTGCCCC | 11060 |
rs554737545 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811988 | AACTAAGAAATTTCC[C/T]GTTTTTGCAGTGTTG | 11060 |
rs554744166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933021 | GGATGTTCCTTTTTT[A/C]CGTGGTGACCTCCTC | 11060 |
rs554750317 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69798430 | AATTTACCAACGATA[A/T]ATTGGTGATGATGAT | 11060 |
rs554751039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873664 | GAGCATTTTTCTCTT[A/C]GAAAACTCAGTGGCT | 11060 |
rs554782596 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69771503 | CCACCCGCCTGGGCC[G/T]CCTAAAGTGCTGGGA | 11060 |
rs554787018 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876896 | AAATATTCAGTAAAC[C/T]ATGCTGCAGACAGAT | 11060 |
rs554797729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814041 | GAAATATGTCAGACA[A/C]CTAAATTCTCAGGCC | 11060 |
rs554830806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893722 | AATTTTTTGTATTTT[C/T]TAGTAGAGCCAGGGT | 11060 |
rs554839662 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69904686 | CTAGTGTGCATTTTC[-/A]TCTGGCCACTTTTGC | 11060 |
rs554848024 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902306 | TGAGTGGATTGGGAC[A/G]TAGGGTTGGAACATG | 11060 |
rs554858004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778541 | GTAGTGGATAGTGGG[A/G]ATTTGGACCTAATAC | 11060 |
rs554896104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69869248 | GGAAAAAGAGAGTCC[A/G]CATTGAGTATTTCCA | 11060 |
rs554931147 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761650 | ATAATTCATTAAGTT[A/C]TCTGTGCCCTGTAGT | 11060 |
rs554946885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770859 | TCTGTGGGGCTGGGC[G/T]TGGTGGCTCACACCT | 11060 |
rs554963836 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69894976 | CACCATGCTTTTTCT[-/C]CCGCAGCCATTGGCT | 11060 |
rs555011739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860423 | GAATGTGTAGTGACA[C/T]ATAGCAGTGCCATAA | 11060 |
rs555042211 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782764 | AATCTTGGAGCGTGA[-/C]ATTGTTTGACTTTAG | 11060 |
rs555052371 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768770 | AGCCTGTAATTCCAC[A/G]GGGCTTCCAATAGTG | 11060 |
rs555058357 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69918849 | TCCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 11060 |
rs555104920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892030 | ATCTCCTCCACCATA[C/T]TCTAGGTGCCATACG | 11060 |
rs555129215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767319 | ACATTTAACCTTGTT[A/G]AGGTGAAGTGACCCT | 11060 |
rs555146258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939280 | GTGGGTGGAGCCGGA[G/T]GATCCTGCTTTGGGA | 11060 |
rs555161438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783542 | ATACAGCCAGACCCT[G/T]TGTCTAAATAGTAAT | 11060 |
rs555188744 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913285 | TGAGCCACCCACCTC[G/T]GCCTCCCAAAGTGGT | 11060 |
rs555203301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769678 | GCTCTTACTGTGTGT[C/G]CTCTGCTTTACCTGA | 11060 |
rs555259875 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863742 | CCTCCTTGTACCCGT[C/T]GCTGCTGGCAAGCAT | 11060 |
rs555267604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861056 | TTGGGGGCCAGCCCC[A/G]TGGAGATTCCTCCTG | 11060 |
rs555332550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853847 | ATGGAGACAAGAGAC[A/G]CAAGAGGCGGGGAGC | 11060 |
rs555368121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797135 | GTAATATACACTAGG[A/G]TGTCTGTCTAGCTCC | 11060 |
rs555371596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69803131 | TTGATAACTATTAAC[A/G]TTATGATGGATTTGC | 11060 |
rs555373442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811506 | ACCTCCCCACACTTT[C/G]GGAGGCTGAGGTGGG | 11060 |
rs555376870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69830351 | GCCTCGGCCTCCCAA[A/G]GTGTTGGGATTACAG | 11060 |
rs555406943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790198 | GTTGCTGTGAGCCGA[A/G]ACCACACCATTGCAC | 11060 |
rs555407862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866420 | GAGCCACTGCACCTA[C/G]CCTCATTTTATTAGA | 11060 |
rs555410660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803672 | CCCAGACCTGGGAGG[C/T]GGAGGCAGGTTGATC | 11060 |
rs555416257 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942098 | AGAGTGTTCCAGGCA[G/T]TCATTCATTTGGGAA | 11060 |
rs555417171 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69799818 | GGAACGTGATGGACG[C/T]GCCATCTGAATTAGC | 11060 |
rs555426513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817478 | TGGTCTCGAACTCCT[G/T]ACATCAAGTGATCCA | 11060 |
rs555443638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795424 | ATATCCTTATTTGCA[A/C]TAGCCATATTTCAAG | 11060 |
rs555471276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930729 | CATTTAAAATTAGCT[A/C]GGTGTGGTAGCACAC | 11060 |
rs555484217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810806 | GTTGCCCAGACTGGA[A/G]TGCAGTGGCACAATC | 11060 |
rs555484302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788775 | AGTAAGAGATTTTTG[C/T]CGCTTTGGTCACTGT | 11060 |
rs555493438 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817941 | TCTTTTTTTTTCCCT[A/G]CAGTAAATTCCCAGG | 11060 |
rs555504558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905053 | CAGCTGATCAGACCA[C/T]GCCCAAATAAGGCAG | 11060 |
rs555523417 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858216 | GAGTTATTTCTTCCA[C/T]CTGGTTTGTGGTTTT | 11060 |
rs555534208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69840523 | CATCTTTCATCCCAT[A/G]TGGACTTTGGAAAAT | 11060 |
rs555560405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854561 | TTTTTTTAAGTTTAT[G/T]TATTTTTGAGATGGA | 11060 |
rs555625140 | in-del | -/A | 0.391397 | 0.206172 | intron-variant | WWP2 | GRCh38.p7 | 16:69827154 | GAAATGGAAATTATG[-/A]AAAAAAAAAAAACTA | 11060 |
rs555632984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832930 | TGCAAACATGGCTCA[C/G]TGCAGCCTTGACCTT | 11060 |
rs555643826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823131 | GCGAGACTGTGTCTC[A/C]AAAAAGAAAAAAGTA | 11060 |
rs555665141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797743 | AAAATACAAAAATTA[A/G]CCAGGCACGGTGGCG | 11060 |
rs555717661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69907969 | CTTTAAGCCGGGTGC[A/G]GTGGCTCACTCCTGT | 11060 |
rs555726373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932278 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCATTG | 11060 |
rs555726550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923109 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 11060 |
rs555733303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816848 | ATTTATTCTTCCTCC[A/G]TACATTCAAGGTAGA | 11060 |
rs555779591 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881748 | CCAGGCTGGAGTGCA[A/G]TGGCATGCTCTCAGC | 11060 |
rs555780855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908529 | GAGTGATCTATAGTG[C/G]ATCCTGGTCCATTGA | 11060 |
rs555785785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844207 | GGTGACTTACAATAG[G/T]TGGGTCTCACGGGGT | 11060 |
rs555798880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916541 | AGCAGTAGTCCAGGG[A/G]TGAGGTGATACAGAT | 11060 |
rs555812003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884950 | GTGAATTATTTAATT[A/G]TTTAAGCCTATTTCT | 11060 |
rs555825031 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69794875 | AGTAGCCACAGGCAA[A/T]TTGTATATATTGATT | 11060 |
rs555847879 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855860 | GAATTTCTGCTTTAT[G/T]TATTTCGAGGTTATT | 11060 |
rs555853177 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879476 | TATAAGTGGATTAAC[A/G]TGTCCTTTTGTGTCT | 11060 |
rs555874550 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879921 | AATAATTAGGCCTGT[A/G]CATTTAAAAAATGTG | 11060 |
rs555903727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903620 | AAAATACAAAAAAAT[C/T]AGCCAGGTGTGGTGG | 11060 |
rs555942342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935406 | TTACTCACCATTGGC[C/T]GCCAGCTCTCGCTGT | 11060 |
rs555976676 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69915817 | GGCGAGAGGATTGCT[G/T]GAGCCCAGGAGTTTG | 11060 |
rs556002744 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847895 | TGGTGGGGACAAACT[A/G]CATCCAAACCATAGC | 11060 |
rs556016318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775450 | GTCTACTGATGAGCC[C/T]ATCAAGGCATTCTTC | 11060 |
rs556019373 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69789322 | GTAACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 11060 |
rs556023143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877328 | GCTATCTTCCAACTT[C/T]TCTTCTGCAACTTCC | 11060 |
rs556034805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910084 | ATTACTTTGTGTAGC[A/G]CTTTATAGAAAAAAT | 11060 |
rs556036880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904544 | TGACTATTTAAAAAA[A/T]TTTTTTTATAGAGAT | 11060 |
rs556048948 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69822533 | CCTGGCCTGGGTGGG[G/T]TGTGTGTGTGTGTGT | 11060 |
rs556085323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821340 | TGTTGGAAAGAAAAG[A/G]TCCTTTTAGCCACAA | 11060 |
rs556088334 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941518 | GTTACCATGGAAGCC[A/G]CTCCAGGGTGGGTCA | 11060 |
rs556110940 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69896884 | CAAGTGAGGAGAACT[G/T]AAGCAATTTGCCTGG | 11060 |
rs556125907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763470 | GAACGAATGTTCAAA[C/G]TGGACATTCACAGCA | 11060 |
rs556142843 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772784 | AGTCTGGTCCTGAGT[C/G/T]GAGTCCTCCCTCCTG | 11060 |
rs556143569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773729 | TCAAGCAGTCTGCCC[A/C]CATCAGCCTCCCAAA | 11060 |
rs556170214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69815644 | ATACACAAATTAGCC[A/G]GGTGTGGTGGCGGGT | 11060 |
rs556200414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863195 | CATACCTGCCTTCTA[C/T]AACTTTTGCTCACTT | 11060 |
rs556223954 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906095 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 11060 |
rs556227759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765388 | AACCTGTTCTGAATG[A/C]CAGGAATATAGCAGT | 11060 |
rs556237779 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904686 | CTAGTGTGCATTTTC[A/C]TCTGGCCACTTTTGC | 11060 |
rs556263592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869797 | ATCTTGTCAAATTCT[G/T]TTTCTTACTTTAGAG | 11060 |
rs556264647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862210 | AGCTGGGATTACAGG[C/T]ATTCGCCACCATGCC | 11060 |
rs556289129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69762919 | TAAACTTCAGGAGGG[A/T]TCACAGAATCTTGAT | 11060 |
rs556289445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882545 | GTTGAAACCACACAT[C/T]AGCAAAGTCAAAACA | 11060 |
rs556293163 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933879 | GTGTCCCCATACTAA[C/T]CTGAGACACGATGGT | 11060 |
rs556313762 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881283 | TTCTGGTTTGAGTAC[C/T]GGTTCTGCTACTTGC | 11060 |
rs556331497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69801138 | AGGTTCCAGTGAGCC[A/G]AGATTGCGCCACTGC | 11060 |
rs556346426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786391 | CCCTGTAATCCACCC[A/G]CCTCCCAAAGTGCTG | 11060 |
rs556350395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869178 | CAGGCATGAGCCACT[A/G]TGTGCGGCCAACAGC | 11060 |
rs556360050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890290 | ACGCTACCTAACTCC[C/T]GTCTGTTCAGAAAGT | 11060 |
rs556391320 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939211 | TCTTCCTGGAAGCAC[A/G]TCAGTGGGATGGAGA | 11060 |
rs556397301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820688 | AAGCGGTTCTCCCCA[C/T]ATACTACTGTTTATT | 11060 |
rs556410451 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69935649 | TGCAGGGCAGGGTGG[A/G]AGTCCCTCTGTAGGT | 11060 |
rs556423494 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795409 | TAACATTTAAAAATC[A/G]TATCCTTATTTGCAC | 11060 |
rs556428946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888835 | TCAGCCTCCCAAGTA[G/T]CTGGGGCTACAGGTG | 11060 |
rs556447130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69799966 | CAGTACCATATGTGG[C/T]GAATGAATGGCATGG | 11060 |
rs556461945 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941179 | CGCCAGCCTCCAACA[C/T]GGGGACTCTGCCGTA | 11060 |
rs556483425 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69821826 | GCCTCCCAAAGAGCT[G/T]GGATTATAGGCGTGA | 11060 |
rs556486068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793992 | GGACAATCTCAGCTT[A/G]CTGCACTTTCTGCCT | 11060 |
rs556509225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856006 | GCCAGGCACAGTGGT[A/G]TGTGCCTATAGTCCC | 11060 |
rs556525256 | snp | C/T | 0.000341507 | 0.0130628 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939868 | GGATCTTCCACCCTA[C/T]AAGAGCTACGAACAG | 11060 |
rs556528337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69857476 | TTGGCTCCCTGACTA[C/T]TTGATAATGGAGTGT | 11060 |
rs556531978 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933485 | GGATCGGGGTTGGAA[A/G]TGTGTTGCTGTGTAT | 11060 |
rs556538231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841511 | GGTGAGATCAGAGAA[A/G]CAGGTCAACTCAGAT | 11060 |
rs556545112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847428 | TTTTTAATTTTTTTG[A/G]GATGGAGTTTCACTC | 11060 |
rs556551124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806681 | TTCATGAGATTTTCA[A/G]ATTTATTAGAATAAG | 11060 |
rs556561438 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788906 | CCATCACAGATGGGA[A/G]AGTGGCTCTCAGTAT | 11060 |
rs556594384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849263 | GAGCTGAGCCTTGGG[C/T]ACTAGGCCATTCTCA | 11060 |
rs556613157 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843548 | TATCACTTGCGGAAA[A/G]TAGGTGAGTAACTGG | 11060 |
rs556636521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69807292 | CACCTGCCTCAGTCT[C/T]CCATACTGCCGGGAT | 11060 |
rs556668187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932979 | CTGTTCGGTGGTGGC[A/G]TTGCCTTCTGCGCTG | 11060 |
rs556684168 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761917 | CTTTTTTTAGTATAA[A/G]TATGTCCCATTCTGT | 11060 |
rs556691461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869772 | ACGGTTAAGATTTTG[G/T]TTTATGTTCATCTTG | 11060 |
rs556710046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69813540 | CTGGAGTGCAGTAGC[A/G]CAATCTCAGCTTCCT | 11060 |
rs556732870 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WWP2 | GRCh38.p7 | 16:69846686 | AGATTGCGCCACTGC[A/C]CTCCAGCTGAGTGAT | 11060 |
rs556737622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868788 | TGTGCTCATTCCACT[A/T]TTGAGGAGGAGCTGT | 11060 |
rs556758220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69892613 | ATCTTGGCTCACTGC[A/G]GCCTCAGCCTCACGG | 11060 |
rs556772234 | in-del | -/T | 0.20571 | 0.246046 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774048 | TGGTGGTCAGTGTTG[-/T]TTTTTTTTAATGCTC | 11060 |
rs556789458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929109 | TGCCCGGCTTCCATG[C/G]TGCACACAGCTGGGA | 11060 |
rs556873195 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762283 | TGCGAGCCTGGCCAG[C/T]CTCTTCCGGGTCAGG | 11060 |
rs556893670 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791479 | GTGATCCACCCACCT[C/T]GGCCTGCCAAAGTGC | 11060 |
rs556921732 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69918104 | GTGTTTAAGGAATCA[A/C/T]CGTGTCTAAAACTGA | 11060 |
rs556923305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910181 | AATCCCAAATGTCAC[A/T]TCATCTATCCATATT | 11060 |
rs556926760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928460 | GTCTGCCCCTGGAGC[A/C]CAGACTCCTCCCTTG | 11060 |
rs556929392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919142 | AGCCACCATCCCCGA[C/T]CACATTTAAATTTTC | 11060 |
rs556947067 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922307 | GCCCTTCCCAGACCT[G/T]TCTTACCCTCAGCTG | 11060 |
rs556960146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783998 | AATTTAACAGCATCA[G/T]TTCTCAAGTGTGGTC | 11060 |
rs556962562 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69817647 | ATTACTAGCAGCACT[G/T]TTTGTTAAACTCTTT | 11060 |
rs556974840 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874433 | TTTCCACAGACTTGC[A/G]AGATTTATTTAGCAG | 11060 |
rs556982945 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910733 | TTCTTCTTAACCTCT[C/G]TTGTCTAGGAGGGAC | 11060 |
rs556999901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791878 | TCTGCACCTGTCCAG[C/T]ACATACTTCTAAAGG | 11060 |
rs557000096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805446 | AACTTTCTGTTTTAG[C/T]GGTGATAGAGAAATG | 11060 |
rs557006928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777518 | GTTGGCGAGGCTGGT[C/T]TCGAACTCCTGACCT | 11060 |
rs557013383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69771296 | CTGTGTCTCCCAGGC[C/T]GGAGTGCAGTGTGCT | 11060 |
rs557025636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790134 | CGCATGTAATCCCAG[A/C]TACTTGGGAGGCTGA | 11060 |
rs557032958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847287 | ACGGGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 11060 |
rs557056285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69917515 | ATGGATCCCCAAATT[A/G]GAAATTGAGAGCTAA | 11060 |
rs557066990 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762176 | CTGGGACCATCCGGT[G/T]AGCAGAAACCCTTCC | 11060 |
rs557068422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69783344 | GTAATATGGTGAATT[A/G]ATAACCATGTTTTAA | 11060 |
rs557091433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893669 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGAGTACAG | 11060 |
rs557107539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906345 | CCACAGTGCTGGGAT[G/T]ACAGGTGTCAGCCAC | 11060 |
rs557123022 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899725 | GAGTGAGACTCCGTC[C/T]CAAAAAAAAAAAAAA | 11060 |
rs557135025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925176 | GTACCGCCTCCTCCC[C/T]GTCGCTCTGCCTTTT | 11060 |
rs557138164 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938093 | AAAATAGCGATTACA[C/G]GTATTCTTAGTACAT | 11060 |
rs557139914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778420 | ATGCAATTACTTTCC[A/G]TGGCTATTAGCAGGG | 11060 |
rs557155508 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69879766 | GTGATTTTGTATTTA[A/T]CATGTCATGCCCATG | 11060 |
rs557168254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820004 | CAGTGCATTAAGAGG[A/C]TGAGGCGGGGGCAGG | 11060 |
rs557171198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912312 | AAAACAAAACAAAAC[A/C]TCATTGGTTTTAGAT | 11060 |
rs557176090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832051 | CCAGGCGGGTCTCGA[A/C]CTCCTGAGCTCAAGC | 11060 |
rs557185229 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877168 | TCAACATTGAAAAGC[G/T]GTTGTTTCGTGTGGC | 11060 |
rs557195011 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902648 | AGTTTGATTGAAAAG[C/G]CTTTTAATCTCAGTG | 11060 |
rs557221794 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896319 | AGACAAGGTCTTGCT[A/G]TGTTACCCAGGCTGG | 11060 |
rs557240653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69913388 | ATGCCTGTGTTCCCA[A/G]CTACTTGGGAGGCTG | 11060 |
rs557246478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818285 | TGATCTTGGCTCACT[A/G]CAACCTCTGCCTCCC | 11060 |
rs557246482 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852880 | TACTTTCATGCTACG[A/G]TGGTATGTTAAGTAG | 11060 |
rs557260485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875365 | CGATGTTGATGGCTG[C/T]TGACTGATCAGGATG | 11060 |
rs557283911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792464 | CTGTGTATAAAGATA[C/T]ATTTCATGAAAGAGA | 11060 |
rs557289812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69784950 | TTTAAAGAAAAGAAA[G/T]AGTGGTCGAGTGCAG | 11060 |
rs557308939 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897765 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGCAT | 11060 |
rs557316071 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69767041 | TAGGGGTTTTGTTTT[G/T]TTTTTTTTTAATCTT | 11060 |
rs557333752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768507 | CCCAGCTACTTGGGA[A/G]CCTGAGGCAGGAGAA | 11060 |
rs557353659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824804 | GAGACAGAGTTTTAC[C/T]CTGTCACCCAGACTG | 11060 |
rs557379548 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863856 | TACTTAGCATAATGC[A/G]GTTGTGATTCACCTC | 11060 |
rs557392316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69866923 | GCTCACTGAAACCTC[C/T]GCCTCCTGGATTCGA | 11060 |
rs557404818 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816759 | TATACACACGTATAC[A/G]TATACACATACACAC | 11060 |
rs557441849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904442 | GGTGTGATCACGGCT[C/T]ACTGCAGCCTCCAAC | 11060 |
rs557442304 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931397 | TTTCATTCCTAGGGC[A/G]CATGCTATTGCCTCC | 11060 |
rs557448497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925829 | CACTAAGATATTTTG[A/G]CACTGCCTAACTCCC | 11060 |
rs557454805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839699 | GAATAAGCCCCTGCA[A/G]TCCCTCATCTAGATG | 11060 |
rs557458115 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69858957 | TAACTGTATGAGGGC[G/T]GCTGAACTAGACCAG | 11060 |
rs557472816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880466 | TTCAAAACAAATTTC[A/G]GACTTTGAATTCTTT | 11060 |
rs557477825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766232 | CTCTTCCTCTCACAC[C/T]CCACATCCAACTCAG | 11060 |
rs557481795 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69762770 | GAGCTGGAAGGGGGT[A/G]CCTGAAAATGGGTTT | 11060 |
rs557484065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891903 | ACCCTGACATCCGTT[C/T]AGTCATCAAGCCCTG | 11060 |
rs557529718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69774792 | CTGGACAACTTGGTA[A/C]AATCCTATCTCTACT | 11060 |
rs557543615 | in-del | -/TT | 0.491316 | 0.0653198 | intron-variant | WWP2 | GRCh38.p7 | 16:69821725 | TCTTTTCTTTCTTAC[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs557545483 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69795097 | AAAAGTTAGCCAGGC[A/G]TGGTGTTGCGCACTG | 11060 |
rs557558101 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829885 | TACTTGAACCTCCTG[A/G]GTTCAAGTAATCCTC | 11060 |
rs557559172 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846582 | AAAAATTAGCTTGGC[A/G]TGGTGGCGTGCACCT | 11060 |
rs557575174 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761468 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 11060 |
rs557579176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860979 | AAACAGGGAATGATG[C/T]CAGTAGCGAGAAAGT | 11060 |
rs557592879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776838 | CATCTCGAAAAAAAA[A/T]AAATAAAAAAAATTA | 11060 |
rs557620652 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891342 | TCATTTCTAATTCCA[A/G/T]TACCAACAAAGGGTG | 11060 |
rs557635215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796257 | GTGTATGTGTATGAG[C/T]GCAGATACTTCTCAA | 11060 |
rs557652476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867318 | CATTGTGTGCTATGA[G/T]AGAAATTTGTGTCTC | 11060 |
rs557663990 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931647 | ACCCCATCTCCTATC[A/G/T]CGTGGCCTGTTAAAC | 11060 |
rs557685038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769052 | GGCTGGGCGCAGTGG[C/T]TCACGCCTGTAATCC | 11060 |
rs557728812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844187 | ATGTTTTCCGTGTCT[C/T]GGTAGGTGACTTACA | 11060 |
rs557740750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69809902 | AGTGGGGAAGCTGTC[A/G]TTAACATGGGACATT | 11060 |
rs557748216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803054 | GAAATTTCTGGTTTG[C/T]ATTGTACCTTGGCAT | 11060 |
rs557829953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801053 | AATTACCCAGGGATG[A/G]TGGTGGGCGCCTGTA | 11060 |
rs557843954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903776 | TGTCTCAAAAAAAAA[A/G]AAAAAGAAAGAAAGA | 11060 |
rs557847892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69823087 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 11060 |
rs557861887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935373 | GCCAGCAGGACAGAC[C/T]GGTAAAACCCTAGAC | 11060 |
rs557880897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874655 | ACGAATGGCATAGCC[C/T]TTCATTGAGACTTGT | 11060 |
rs557898091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909344 | CTGCTCCAAGAAAGA[A/C]TCACCTCCCAGTAAA | 11060 |
rs557934189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69797075 | GGGCAGGATGGGAGA[C/T]GTCTAGATGTGTTTT | 11060 |
rs557983797 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838863 | AAGGGAAGGTAGAGC[A/G]CTTAGGAGAGCTTGA | 11060 |
rs557983855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845820 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACTTGA | 11060 |
rs557990925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844558 | TGGTCTCTGAATTCC[C/T]CTAGTTGATCGACCT | 11060 |
rs558061671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931310 | CACAGCAGCAGGTAT[C/T]GGAATGTTTGTGTCT | 11060 |
rs558069589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851916 | TAAATCTGGGGGGTG[C/G]AGTTTGCAGTGAGCT | 11060 |
rs558085830 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850868 | TTTTTAGAGCACTTT[C/T]AGGTTCCCCCAAACA | 11060 |
rs558093726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822505 | ATCTGGGAATGCATC[A/G]TGGGAGACTTTGCCT | 11060 |
rs558096891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845240 | ACAACGGGAGCACTC[A/G]GTGGAAGTGGCAGTG | 11060 |
rs558117037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937029 | TGCTGATCTGGTGGT[C/T]CTGCGCGGTAACGGC | 11060 |
rs558117628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913647 | TTGATATCCTCAAAG[A/G]TTTGGGAGAAAATAA | 11060 |
rs558124521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930636 | CTCAGGAGTTTGAGG[C/T]TGCAGTGAGCTATGA | 11060 |
rs558137727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890247 | ATGTGACCTTTACTA[C/T]GTACGTATTGTTTTC | 11060 |
rs558142374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69786827 | AGTCTATCCTAAGAC[C/T]TGTCCAGGTTCATTA | 11060 |
rs558155246 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811815 | CAAAGAACTCCTCAA[C/T]GTCGTCCTTCACCCA | 11060 |
rs558174765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914286 | ACAGCTCACCACACG[C/T]CTAGCCCAGAGGATA | 11060 |
rs558200953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69890870 | CCAGAGGCTGAAACA[C/T]GTTTCTGAGGTAGAG | 11060 |
rs558208509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800288 | AACTCCCTGATTGCT[C/T]TGTCTTCTGAATTGG | 11060 |
rs558233684 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858516 | GAGAAGAGGGGGCGC[C/T]CTTTATCACAGCCGC | 11060 |
rs558248765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920558 | GTCCTTTGACTTAGA[A/G]ACAAGGACGTATTTT | 11060 |
rs558259249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69836086 | GGGATTACAGACGTG[A/G]GCCACCGTGCCTGTG | 11060 |
rs558278696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69896183 | CTGGAGTATAGTGGC[A/G]TGATCATAGCTCACT | 11060 |
rs558285578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69814743 | TGGGCCTCCTCCCTT[A/G]TTGCTCCGTGAGGAT | 11060 |
rs558295392 | in-del | -/TG | 0.0035928 | 0.0422314 | intron-variant | WWP2 | GRCh38.p7 | 16:69803584 | TCCACCCTGCTTTTT[-/TG]TGTGTGTGTGTGTGA | 11060 |
rs558298944 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834966 | TGCCCATCTTGTTCC[C/T]GTTGAGTCACTAGAA | 11060 |
rs558330953 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873888 | GTCCTTGAGTCACTC[C/T]TGGACATTTCAATAG | 11060 |
rs558373720 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69815586 | AGGTCAGGAGTTTGA[C/G]ACCAGCGTGGCCAAT | 11060 |
rs558388910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922234 | TTTTGTTCTGCATCC[A/G]TCTGGTGCATCCTTA | 11060 |
rs558395930 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69862373 | CTGGCCCTTGTTTTG[-/T]TTTTTTTGAGATGGA | 11060 |
rs558411398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877482 | CCTATCACTTTTCTT[C/G]GTAAGGCTGTTTTAC | 11060 |
rs558434322 | snp | G/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69775116 | GTGGAGAAATACGAT[G/T]GGACAAAAGGGGTAT | 11060 |
rs558436730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69908411 | AGGGTCCTCAGCTTT[C/T]ATCATGTTCCTAAAG | 11060 |
rs558439197 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69916449 | AGCAGGAGTGTGACC[A/G]AAGGGCTCAGTCTAG | 11060 |
rs558444386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821274 | CCACACCCTCAACTT[C/G]TCAAAGTTGCAGCCG | 11060 |
rs558464665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781207 | GAGGAGGCCTGTGTG[G/T]CAGTAATCACAGCAT | 11060 |
rs558499677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900585 | TGGAGTGCAGTGGTG[C/T]GATCTCAGATCACTG | 11060 |
rs558502682 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918106 | GTTTAAGGAATCAAC[A/G]TGTCTAAAACTGAAT | 11060 |
rs558505755 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762250 | AGGTGCCCAGGCCAG[A/G]CCTAGGTGGCCCGCA | 11060 |
rs558505961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69903074 | GTTCCTCTGGCAACT[A/G]TTCTTCTCGCTAAGC | 11060 |
rs558514002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788629 | ATCCCCTGATCCAAC[A/G]CCACCTTTCTCATTG | 11060 |
rs558522987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779932 | ATAAAATGGTTAGAG[A/G]TGAAGATAACAAACA | 11060 |
rs558547079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69779231 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCGT | 11060 |
rs558577630 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801402 | ACCATGGCCTGGCTG[G/T]ATTTCATATTTTTAG | 11060 |
rs558608382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875251 | TATGTCTAAAAAATG[A/T]ATACACTTTAATTAA | 11060 |
rs558629930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812989 | GATTTTACTCTGATG[C/T]CTATAGATTTTTATT | 11060 |
rs558647966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794930 | GCTTTAAAAATATGT[C/T]TGGGGACTGGGCAGT | 11060 |
rs558655983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69786266 | TCTCTGCCTCACCCT[C/T]CTGAGTAGCTGGGAT | 11060 |
rs558667341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769795 | GTAGGTATGATTTTG[G/T]GAAATATATATTTAG | 11060 |
rs558671588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868549 | CTCCTGGGGGCTGCA[A/G]GTTCCAAATCAGAGA | 11060 |
rs558688210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798943 | CGACTTTTTCTACCT[A/G]TGGTACCCAAGGTGA | 11060 |
rs558688674 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69902731 | GATGAAAAATTGATA[A/C]CAGTGTCACTTTCTT | 11060 |
rs558726570 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69876318 | AGTTATAGCCTTATA[A/C]AATGTATTTGGTTTT | 11060 |
rs558744289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69888761 | CCAGGCTGGAGTGCA[A/G]TGGCACGATCTCAGC | 11060 |
rs558753627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69808138 | ATTCTGACTTCTATC[A/G]CTATTGTTCAGCTTT | 11060 |
rs558789302 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916186 | GGGAGTCAATGGAAG[-/TGT]TGTTGTTGTTGTTGT | 11060 |
rs558796381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863596 | TAGTGAGCCGAGATT[A/G]CGCCACTTCACTCCA | 11060 |
rs558821782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69907963 | CTGTGACTTTAAGCC[A/G]GGTGCGGTGGCTCAC | 11060 |
rs558822122 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771805 | AGTGCGGGAAGGTGA[A/G]TTGGGTGGGGGAAAT | 11060 |
rs558822151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895534 | TTTGGGAGGCCGAGT[A/C]AGGAGGATTGGTTGA | 11060 |
rs558843631 | snp | G/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941250 | CCATGCCCCACCGGG[G/T]TGCTGGGGCAGTAGT | 11060 |
rs558848921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69807185 | GGGTTACAGGCACAC[A/G]TCACCATGCCCGGCT | 11060 |
rs558875476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869730 | AGCACAAAAGGGCTT[C/T]TTTATTCCCAATATC | 11060 |
rs558883980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906747 | TAGCTGGGCCTCGTG[G/T]CATGCACTTGTTTTC | 11060 |
rs558926806 | in-del | -/ACAT | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69816773 | CATATACACATACAC[-/ACAT]ACACATATACACACA | 11060 |
rs558946188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819825 | CATGAATTTTTCAAT[C/T]GCCCCAGTGAGATCC | 11060 |
rs558959375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69893154 | CATCTTCAAGTGTCA[A/G]CTTAATCAGTAAATC | 11060 |
rs558967473 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768584 | CACTGCCCTCTAGCC[C/T]GGGCAACAAGAGCGA | 11060 |
rs559012728 | snp | A/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838059 | GAACCATGTCTCTAT[A/T]AAAAAAAAATTAAAA | 11060 |
rs559050443 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925703 | CCACTGTAGCATCCA[C/T]CCACCATCGCTAAAG | 11060 |
rs559052420 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900669 | CTGGGACTACAGGTG[C/T]GTGCCACCATGTCTG | 11060 |
rs559062669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69831603 | CTCATCCTTGCTGCA[C/T]GTACAAACTCTTCTC | 11060 |
rs559071535 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827827 | AATGACAAGGCAGCA[A/G]TAATGATGTGAACTG | 11060 |
rs559082287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69867056 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 11060 |
rs559098012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782999 | AATTCTCATATGAAG[A/G]GCTTTTGTCCTTTTT | 11060 |
rs559110642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826651 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 11060 |
rs559144495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867621 | AACCACTTTGGGGAG[C/T]GTGGGTCCTGGTCGT | 11060 |
rs559169385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898840 | TCTGGAGTAGCTGGG[A/G]TTACAGGCATGTGCC | 11060 |
rs559176536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69854709 | GCACCTGCCACCACG[C/T]CTGGATAATTTTTGT | 11060 |
rs559182472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806616 | TTGTTCAGCTTCTTT[G/T]TTTCGTCTTGACTCA | 11060 |
rs559223305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839250 | AAAGGCTGATTCCCT[C/G]TTGGTAATTATTAAA | 11060 |
rs559265134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905371 | TGTGTACCTTCTTCC[A/G]GGAGATCAGATCTGA | 11060 |
rs559265435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69765451 | TCTTCAATTTTATTA[C/G]AGAAGGGCACATTGA | 11060 |
rs559295294 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878193 | TCACTGGTCACAGAT[C/T]TCCATGACGGATATA | 11060 |
rs559306952 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69859955 | CTCAAGGGTGTGGCA[C/T]CTTGTCATATTCACA | 11060 |
rs559309051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811883 | TTCTGAGCCATTTTA[A/G]AGTAAATTACAAACC | 11060 |
rs559328664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848077 | ACAACAAAATGAGAA[G/T]AATGCATTTAATTTG | 11060 |
rs559345409 | in-del | -/T | 0.095182 | 0.196294 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774048 | GGTGGTCAGTGTTGT[-/T]TTTTTTTTAATGCTC | 11060 |
rs559358339 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856360 | AATGGGAATGTTCTA[C/T]GTCTCAGTTGTGGTG | 11060 |
rs559389326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917112 | TTGCAAGTAACAAAA[C/G]TTGTTAGCAACATTG | 11060 |
rs559391108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790341 | CAATAAAATAAGCTA[C/G]AGAAAAAATCATAAG | 11060 |
rs559419443 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69817949 | TTTCCCTACAGTAAA[-/T]TCCCAGGCATGCAGT | 11060 |
rs559441093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916080 | AAATAAATAAAAATC[A/T]CTAGTTTAGACAAAT | 11060 |
rs559517512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816485 | ATATACTTTATATAT[A/G]TAATATATAAACATA | 11060 |
rs559531109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851404 | TGCATAGTTTTGCCA[C/T]TTCCAGAATGTCGTA | 11060 |
rs559539477 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922755 | TTTCAAGTTGTACTG[C/T]GTACCTTAGGGAAGA | 11060 |
rs559545045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906159 | CTCACTGCAAGCTCC[A/G]CCTTCCGGGTTCACG | 11060 |
rs559560864 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874798 | CCGTGGTCAGATTCC[A/G]ATTCTTCATCTTTAA | 11060 |
rs559563010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832181 | TGTTTGATAGTGGCC[A/G]GTTACTAGAACAAAA | 11060 |
rs559581003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824954 | TTTTGTATTTTTGGT[A/G]GAGATGGGGTTTCAC | 11060 |
rs559581171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817905 | CCAGCCTAAATTCTT[A/G]TAAAGATACCTTTAT | 11060 |
rs559581520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781410 | GAGTGCGGTGGCACA[A/G]TCTTGGCTCACTGCA | 11060 |
rs559597803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783681 | CCAGGCTTGGTGGCT[C/T]ATGCTTGTAGTCCCA | 11060 |
rs559603214 | snp | C/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925179 | CCGCCTCCTCCCCGT[C/T]GCTCTGCCTTTTCCA | 11060 |
rs559616757 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882207 | GTGATTCACTTGCCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs559631856 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835200 | GGGCCTCTGTAGAGC[C/T]GTCTGCACAGCTGTA | 11060 |
rs559644498 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802750 | GGATTATGACAGGTA[A/C]CTGCCACCATGCCCA | 11060 |
rs559648384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917622 | GACAGGGCCTGCCCG[C/G]CTGTGCTAGGCATCC | 11060 |
rs559650154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823592 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGATTA | 11060 |
rs559665283 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942214 | TTTTTGTTTTTGACA[A/G]ATCACCATGCTGGCG | 11060 |
rs559691658 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69816048 | GGACAAAAGTAAAAG[A/T]CAGCTACAGACCCTG | 11060 |
rs559707220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936759 | CCGGGCCGAAAGGAT[C/G]TCTGTGGCCTGTGTG | 11060 |
rs559742728 | snp | A/T | 0.000926386 | 0.021502 | missense | WWP2 | GRCh38.p7 | 16:69871805 | CTTTGAACCCCCAGG[A/T]CGCACAGACATTCGG | 11060 |
rs559756402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800519 | AAATTACAGAAAGAA[A/G]ACAAAATTTGCCCCT | 11060 |
rs559762200 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815865 | CCCAATTTCCTTTCT[C/G]TGCTTTATTTTCTTT | 11060 |
rs559768112 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772961 | TTTCCCTTTCTGTGG[A/G]TTTTCACCTTTTTGT | 11060 |
rs559822935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69902834 | GGAATCAGGAGGCTC[A/G]TCTGGTTGGTGATAG | 11060 |
rs559823832 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69782054 | TTGGGAGGCTGAGAC[A/G]GGCGGATCACCTGAG | 11060 |
rs559846656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808466 | GGGTGCAATGGTGCA[A/G]TCTTGGCTCACTGCA | 11060 |
rs559881444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69870769 | TAGTAGAAGAGCCTC[A/G]TTTGGTGAAACAGAT | 11060 |
rs559883204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878109 | CACCGTGCCCAGCCC[A/G]AATTTGCTATTTTAT | 11060 |
rs559915090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922369 | GTATCTTAAAATATT[A/G]CTGGAACTTTGTGCT | 11060 |
rs559923177 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69912018 | ACCTTGGCTGGGCTC[A/G]GTTGCTCACGCCTGT | 11060 |
rs559940264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802627 | TTTTTTTGAGACAGG[C/G]TCTCGCACTGTCGCT | 11060 |
rs559956793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897847 | AGGGAGGCGGAGGTT[A/G]CAGTGAGCCGAGATC | 11060 |
rs559959195 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800072 | GGCGGGGAGAGTTGC[A/G]TCCCAGCGAGCGTGT | 11060 |
rs559976360 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787420 | ATAGGGAAGCCCTGT[C/G]TCTACAGAACATAAA | 11060 |
rs559977848 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817928 | ACCTTTATGCTCCTC[-/T]TTTTTTTTCCCTACA | 11060 |
rs560001424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69904613 | TGGTTTCAAGTGATC[C/T]TCCTGCCTTAGCCTC | 11060 |
rs560002158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794320 | ACTTTGAGCTCAGGC[A/T]TAAAGTTTGAGACCA | 11060 |
rs560006864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69815095 | GCAACCTTCGCTTCC[C/T]GGGTTCAAGCGATTC | 11060 |
rs560018289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891572 | GGTCAGGTACTGGGT[A/G]TGGCAGATGCAGTGC | 11060 |
rs560028705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764556 | TTAAGGAAAAAGATC[A/G]CACAGAAAAAGTTGT | 11060 |
rs560035713 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941831 | GGCCTGGATAGGGGT[A/G]GAAATTCCCTGACCT | 11060 |
rs560039905 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789450 | GGGCAGGCTGGCTTC[A/G]AACTCATGACCTCAT | 11060 |
rs560040636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766347 | TGTCTCCCTCTTCCA[C/T]CCTGGCTGGCCTTCA | 11060 |
rs560043846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859291 | GGCACAGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 11060 |
rs560059585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883873 | ATAAACAGTCAGATC[C/T]GAGTAGTGTTGATTG | 11060 |
rs560060192 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69859933 | CGACGACATACTTGA[C/T]GACATACTCAAGGGT | 11060 |
rs560067405 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837408 | GTCTCAAGGTGTTGT[A/G]TGATGGCTTCTGAGC | 11060 |
rs560096453 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936239 | CCCTTGGTGTCCCAC[A/G]GGCAACAGAGCAGGA | 11060 |
rs560102243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788394 | TGCTCCATTTCACAG[C/T]AGAAGCCGAAGCTCC | 11060 |
rs560144236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764057 | ATTGGGATGGTCAGT[A/G]TTGTCCCTATATCAC | 11060 |
rs560146457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69875763 | CTACTTCTTATTCTA[A/G]CTCTCTTGCTATTTC | 11060 |
rs560148467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882614 | ATGGGTGCTGTGGGC[C/T]TCACAGTGTGGAGTG | 11060 |
rs560221623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844238 | GATGAATGACAGTGT[A/G]ACTGGCAAATCTTGT | 11060 |
rs560240794 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940623 | TTTGTCCATGTATAA[A/T]CTTGAAGTGGTTGTG | 11060 |
rs560280850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842828 | GCATGTGCCACCATG[C/T]CTGGCTAATTTTTTT | 11060 |
rs560359494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902345 | ACAACTGAACCAAGG[C/G]CAGCTACAATCCATC | 11060 |
rs560367155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843817 | GAGGCTGCACTGAGC[C/T]AGCATCAGGGCACTG | 11060 |
rs560403956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69883426 | CACACACACACACAC[A/G]CTCATTTACTCCTAC | 11060 |
rs560404254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778793 | ATTATAGTTGCGCCA[C/T]CACTCCTCGCTAATT | 11060 |
rs560406719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876421 | CTAGGCTGGAATGCC[A/G]TGGCATGATCTTGGC | 11060 |
rs560407415 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781328 | AAAGTTCATTTGCAG[A/G]TCTTTGGCTTTTACT | 11060 |
rs560438690 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836788 | CCTGGGTGATTTTTT[A/G]TATTTTTAATAGAGA | 11060 |
rs560441277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779465 | TTTATCTACCCTGTT[G/T]CTCCTGCCTTCCCAG | 11060 |
rs560472815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828732 | TCTTGAACTCCTCAC[C/T]TCAGGTGATCCACCC | 11060 |
rs560489646 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69928624 | CTAAGAACAGGATAG[G/T]CAGGCCAGGCACGGT | 11060 |
rs560489940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920295 | TGCCCCTCTCCAGCC[A/G]GGGCCCCGCTGTCTA | 11060 |
rs560491771 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794625 | AATCAGAAGTAAGAT[G/T]GAATCAACTATGTCC | 11060 |
rs560504524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914480 | AAATGATTTCCTGCC[A/G]GGCACAGTGGCTCAA | 11060 |
rs560511995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792982 | AGGGTGAGCCACTGT[A/G]CCTGGCCTTTAAACC | 11060 |
rs560521616 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69824527 | CCCCTCCCCCTCCCT[-/C]CCCCCTTCCCTTTGT | 11060 |
rs560527319 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862490 | TCCTGACCTCAGGCA[A/G]TCCAACCACCTCGGC | 11060 |
rs560540393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69785890 | TCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGA | 11060 |
rs560542780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826300 | AGACCAGGCGCAGTG[C/G]CTTATGCCTGTAATC | 11060 |
rs560552116 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930761 | CCTGTAGTCCTAGCT[A/G]CTTGGAAAGCTAAAG | 11060 |
rs560555421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69799058 | AAGGATATATGTGGG[C/T]GTCTGCCTGTTTTGG | 11060 |
rs560566511 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783934 | ACTCCCGGCATGGGC[A/G]ACAGAGTGAGATACC | 11060 |
rs560567188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908068 | CAACATGGTGAAACC[C/T]GTCTCTACCAAAAAT | 11060 |
rs560601378 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886463 | GAAGAAAAAAAAAAA[A/C]CAAACAACTTTCTGG | 11060 |
rs560604948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927779 | TGGTAGCTCTGTAAC[A/G]GCTCTGGGCACCTCC | 11060 |
rs560606497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933779 | GCCCTGGTTCACTGT[A/T]GGTCTGAGCCTGCCC | 11060 |
rs560613341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69786431 | GGCATGAGCCACTGC[A/G]CCCAGCCAATCTTTT | 11060 |
rs560641348 | in-del | -/CTTC | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69920939 | TGGTCTTTTTGGAGT[-/CTTC]CTTCCTGCCTGCCTC | 11060 |
rs560657012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833820 | GGCACTGTTTGCAGC[C/G]CCTGCCTGTGACTTG | 11060 |
rs560659814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820949 | GTGTCCGGCTCACCT[C/T]GGAGGCTGACAGCAG | 11060 |
rs560661784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909172 | CTTCGTGAGAATGCC[A/G]CCAAGTTATCCAAAA | 11060 |
rs560677845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842294 | CAGAGCTTAGGATCC[G/T]TATTTATTTTTTTTT | 11060 |
rs560684787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867768 | AAAACCATTTGTGGA[A/G]TTTGGCCTGACTGGC | 11060 |
rs560694004 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP2 | GRCh38.p7 | 16:69869349 | TTCTCCCTTTTTCTC[C/T]TTTTTTTTTTTTGTT | 11060 |
rs560696773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821403 | GAATGTTCCAACAAT[C/T]CTGCACCCTGTGTCA | 11060 |
rs560730168 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918995 | ATTACAGGTGCCCAC[C/G]ACCACACCCGGCTAA | 11060 |
rs560733489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827283 | GCCCCTTTGTATACT[A/T]ATTTTTACATGATTT | 11060 |
rs560757401 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772212 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs560758421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847714 | CGCCTGGCCAGGCTC[A/T]TTTTAATAACCCATT | 11060 |
rs560767094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814261 | GAACTCCTGGGCTCA[A/G]GCGATCCTCTTGCCT | 11060 |
rs560781900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918528 | TTAAGTATCACAATA[A/G]AGACTGTACAGCTCA | 11060 |
rs560797141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907655 | CAGGAGTGTGGGGAT[A/G]AGTGGTCCTTGGCTG | 11060 |
rs560838424 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912813 | ACTTCCAGAGGCCAA[A/G]GCAGGAGGATCTGGA | 11060 |
rs560848093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784967 | GTGGTCGAGTGCAGT[A/G]GTTCACACCTGTAAT | 11060 |
rs560861232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913807 | GAGCATGGTGGCTCA[C/T]GCATGTAATCCCAGC | 11060 |
rs560872877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69809251 | TAGGATGACAATGGC[A/G]TACGTAGCCTATGTA | 11060 |
rs560880609 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813644 | TTTTTATTTTTTGTA[G/T]TTTTGTAGAGACAGG | 11060 |
rs560894584 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69854083 | GGGCACAATTCAGGG[C/T]ACGTGAGTGCTAGTT | 11060 |
rs560907032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69763000 | TTCTTGGGAGCCTAG[C/T]CCTTCAGCTCATTTT | 11060 |
rs560907071 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893858 | CCTCAGAATGCTCTT[C/G/T]TCTGTTCATAAAGGA | 11060 |
rs560924399 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796104 | ATATTAGTATTATAA[A/G]AAGTTAAATGTCCTG | 11060 |
rs560927020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898760 | CCATGCTGGAGTGCA[A/G]TGGCGCAATCTTGGC | 11060 |
rs560959179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868289 | CCCAGCCCATCATTC[A/C]GGGTAAGCCGCTATC | 11060 |
rs560973234 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP2 | GRCh38.p7 | 16:69889997 | TCTCACTCTGTTGCC[C/G]AGGCTGGAGTGCAGT | 11060 |
rs560988818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899680 | GTTGCAGAGCCAAGA[C/T]TGTACCACTGCACTC | 11060 |
rs560989299 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798597 | TTTTTAAAGCAATAA[C/T]TAAAAAGAGCCGGAA | 11060 |
rs560991837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777110 | TATATACACATATGT[A/G]TATATACAATACACA | 11060 |
rs560997231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804279 | TGGTCACCTCTATTT[C/T]TTCCTAGGTGTTTAT | 11060 |
rs561015399 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891429 | GCAGAATGCCTTTAT[A/C]TTTTATGAGGATATA | 11060 |
rs561015734 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914634 | TGGTGGTGCGTGCCT[A/G]TAGTCCTAGCTACTT | 11060 |
rs561028847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69784380 | GCTGGGAATACAGGC[A/G]TGAGCCACTGTGCCT | 11060 |
rs561061643 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769479 | AATAAAATATTGATA[C/T]TGGTGTGTAATTTCT | 11060 |
rs561065794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919339 | CCTGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 11060 |
rs561070112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811249 | GCTTTCCCAGAATCT[C/T]CTACTTTCAAGGAGG | 11060 |
rs561113845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806868 | GGATTTGTCAGATAC[C/T]ATATTTTGTAATATT | 11060 |
rs561121961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69770081 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA | 11060 |
rs561136982 | in-del | -/AAG | 0.00874735 | 0.0655527 | intron-variant | WWP2 | GRCh38.p7 | 16:69763068 | TTTAAAAAACAAAAA[-/AAG]AAAATAAATTAAAAA | 11060 |
rs561138636 | snp | A/C/T | 0.000215842 | 0.0103865 | intron-variant | WWP2 | GRCh38.p7 | 16:69937504 | CGAGTGGACGATGCG[A/C/T]GGGGAGGGACCTGCC | 11060 |
rs561143552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926246 | ATGATGAGACTTAGC[A/G]CATTTGATAGAGCTG | 11060 |
rs561176831 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852010 | AAACAAAACAAAACA[A/G]AGTTTTTAACTTGCT | 11060 |
rs561178781 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69894327 | CTCAAGCGATCTTCC[C/T]GCCTTGGCCTCCCAA | 11060 |
rs561183138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906958 | AGTAGGAATGTAATA[C/T]TAAAAATATTTGTCA | 11060 |
rs561218929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861316 | AAGCCCAACATACGG[C/T]CTGGAAGTAGATTGG | 11060 |
rs561233670 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69804982 | TTTCTTTTGTAATCT[G/T]TCAGTTTACTGAGTC | 11060 |
rs561258081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813102 | TGTAGGTATGTATTA[C/T]CAGCTTCTACTCATG | 11060 |
rs561273368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69852428 | TGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTT | 11060 |
rs561298093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790580 | GTTTAGCATCTTTTT[G/T]TTTGTTTGTTTTTGA | 11060 |
rs561307719 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850061 | ACTTGATATACATGA[A/G]TGCCAGGCTCTGAGC | 11060 |
rs561321191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884404 | TGAGGTGGGAGGATC[A/G]CTTGAGCTCAGGAGT | 11060 |
rs561325459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69882073 | GATCCACCTGCTTTG[A/G]CCTCCGAAAGTACTG | 11060 |
rs561350280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859438 | CGCATGCCTGTCATC[C/T]CGGTTACTCAGGAGG | 11060 |
rs561352603 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69813905 | ATAGGTAAAATTTAC[-/TA]TGTGATAAAGATGGC | 11060 |
rs561382256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69878536 | TTTTCTTTTTTAAAA[A/T]TTTCTTATAGAATGG | 11060 |
rs561392791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846391 | AGCCAAACAATACAT[A/G]TTGTATGGATACCTT | 11060 |
rs561407738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797407 | GCTTGTAGCTCCCTG[G/T]CTATGTAGAGTGGGA | 11060 |
rs561410828 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880489 | AATTCTTTGAAGCAC[A/T]GTAGGATGTAAGTAG | 11060 |
rs561418061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866986 | GGGACTACAGACATG[C/T]GCCACCAGGCCTGGC | 11060 |
rs561432270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886278 | TAGAGATGAGTCCTC[A/G]CTAGGTTGCCCAGGT | 11060 |
rs561442147 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870810 | ACAGGGAGGCTTAGA[C/T]ATTTTCACTGAGTGG | 11060 |
rs561497297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795804 | TGTTGTGCCCCACCA[C/T]GCCCAGCTAGTTTTT | 11060 |
rs561498225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880785 | CTTTACTGTGGCCCA[A/C]ATGTTACGAGCTGAT | 11060 |
rs561502588 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836745 | TCAGCCTCCCAGGTA[A/G]TGGGGACCACAGGTG | 11060 |
rs561503264 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69886859 | ACGTTCACGAAGAAT[C/G]TGGATAGCCACTTGT | 11060 |
rs561534505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69853221 | GAAAAGGATTTAATA[C/T]GGGGAATTAGATGCT | 11060 |
rs561583597 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848404 | GTGGTGAGCCCAGAT[C/T]GTGCCATTGCACTCC | 11060 |
rs561600878 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938180 | TACAATTAACTATTA[A/T]TTTTTTTTTTTTCAA | 11060 |
rs561604386 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69936178 | CTTCTCCTTGAGTCA[A/G]GGAGCTGTCCCCTGT | 11060 |
rs561635471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893137 | GTCCATTAATTCCTA[G/T]ACATCTTCAAGTGTC | 11060 |
rs561639913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782187 | ACCAGGGAGGCTGAG[A/G]CAGGAGAATCTCTTG | 11060 |
rs561648897 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838282 | ACTGATGCTCAGGTT[A/G]GGTAGTTTGCTTCAC | 11060 |
rs561670528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931354 | GACACTTGTCTAACC[C/T]GGAGCTGGCTGTCTC | 11060 |
rs561697828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891490 | AGTGCCCAAGTTCTA[C/T]ATTCGAGGTTTTACA | 11060 |
rs561716343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845421 | TGTCCTTGCTTTCTG[C/G]GGGCAGAGAGAATGA | 11060 |
rs561724054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909892 | ATCTGTACAAACTAG[C/T]CGGCACACTATGATG | 11060 |
rs561732765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69796415 | ACACTTCGATATCCC[G/T]CAGCTAGGCAAGATC | 11060 |
rs561743210 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69829647 | GAAACTTTTCCTGAT[A/G]TCCTGACCAGGCCAA | 11060 |
rs561754293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69866095 | TTTTAAGGTTTCTCT[A/G]GCGTCTTCTTGGCCA | 11060 |
rs561775939 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803030 | TTTACCTTCCCATCA[A/G]CAGTGGCTGAAATTT | 11060 |
rs561793797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69905136 | CCTCTAAAGACTTGC[C/T]GCTCACACTGCTTGG | 11060 |
rs561806387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930922 | GGGAGGAAGGGACTA[C/T]CCTGTTTATTCCGAA | 11060 |
rs561811001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929753 | GGATGGAGGGCGGCC[C/T]GGCTGGCGGGTGTTG | 11060 |
rs561852743 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810455 | TTTTGAGACGGAGTT[C/T]CGCTCTGTCCCCCAG | 11060 |
rs561856544 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837312 | CTCAGGTGATCCTCC[A/T]ACCTCAGCCTCCCAA | 11060 |
rs561928800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924484 | CTTGTTTTATTTAAC[A/G]ACCAGAACTTTTTGA | 11060 |
rs561940458 | in-del | -/TTTG | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69832132 | CTGCGCCCTGCCTTC[-/TTTG]TTTGTTTGTTTGTTT | 11060 |
rs561942824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69872820 | TTGGCTCTGCTTCCC[C/T]GTAAGTGAGACGGGA | 11060 |
rs561949823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69858370 | CGTAGTAGCAGCTCA[A/G]TAAATATTTGCTGAG | 11060 |
rs561970110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831469 | TTTTTTCTTTTGTTG[A/G]AATAAGGACGGCAAT | 11060 |
rs561972602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69822104 | ACTCGTGGGCTCAAG[C/T]GATCCTTCCACCTCA | 11060 |
rs561987089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839187 | AGGGAGGTTCAGATA[C/T]GTGGTTTTGTAAGGT | 11060 |
rs561997130 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764486 | GTGTAAGTCACCATG[A/C]CCAACTGAAAGTTTT | 11060 |
rs562028782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864165 | TTGATCTCAGGAGTT[C/T]GATATCAGCCTGGGC | 11060 |
rs562047222 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778814 | CTCGCTAATTTTTGT[A/G]TTTTTCATAGAGACG | 11060 |
rs562057895 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830326 | CAAACTGGTCTCAAG[C/G]CATCCTCCTGCCTCG | 11060 |
rs562065877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69922271 | AAAAAAAATGCCTGC[A/G]TTCCACGCTGCAACC | 11060 |
rs562083172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781332 | TTCATTTGCAGGTCT[A/T]TGGCTTTTACTCTTT | 11060 |
rs562106378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814220 | GGCTGCAGTGCAGTG[A/G]TGTGATCATAGGTAA | 11060 |
rs562153097 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903198 | AAGATGGAAGGGTGG[A/G]CCTTATCTGGGCCTG | 11060 |
rs562158713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69787519 | CGCTTGAGCCTGGGA[G/T]TTCAAGGCTGCAGTG | 11060 |
rs562162856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883853 | CTAACTAGATTTGCA[C/G]CTGCATAAACAGTCA | 11060 |
rs562175900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921748 | ATCACACGGCCGACA[A/G]TTTCTGGGGCATCTC | 11060 |
rs562185602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897143 | ACAGAATCTGTGTCA[C/T]CCAGGCTGGAGTGCA | 11060 |
rs562196818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913685 | TGTGCAACAAGAACA[A/G]GAGGCCATGAAATGG | 11060 |
rs562199981 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774230 | GGCCTCTTTCCTTCC[A/C/T]TGTATTCCCCAGACA | 11060 |
rs562240326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914673 | GAGGTGGGAGGATCA[C/G]TTGAGCTGGGAGGTC | 11060 |
rs562242965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903888 | TATTAGAGTTTTCCA[A/G]ATAGTGACTGAAAAA | 11060 |
rs562253703 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69813781 | TGGCCTCTGGTGTTG[A/G]TTTCATGCTAAAATG | 11060 |
rs562263865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815958 | AGTCAGGGTCTTACT[A/G]TGTTGCCCAGGCTGG | 11060 |
rs562271259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816476 | TATAAATATATATAC[A/T]TTATATATGTAATAT | 11060 |
rs562279083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69830455 | ACTGGCTTTGTAAAA[A/G]TGAGGCTATTTTCTC | 11060 |
rs562311594 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920622 | CCAAAATTTCTCATT[-/A]AAAAAAAAAAAATGG | 11060 |
rs562313133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810073 | AGCATCTTTTCCTGG[A/G]GAAGGACCTGATGGG | 11060 |
rs562325074 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | WWP2 | GRCh38.p7 | 16:69908818 | TGACCACAATACCAA[C/G]ACCACCACCTGGGAG | 11060 |
rs562327939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766325 | TGATGGCAACAGCCT[C/G]CTAACTTGTCTCCCT | 11060 |
rs562381650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69902776 | CAAACCAAGACAGTC[A/G]GAGGCTCCATCTATG | 11060 |
rs562381855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909100 | AGTGTTGATGCATTC[C/T]GCCGTACCCTATGCC | 11060 |
rs562385366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903365 | CCTTCATATTAAAAC[A/G]TTAGCCAAAGTGTAA | 11060 |
rs562429787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793220 | TAGCTGGGTGTGATG[G/T]CAGGCGCCTGTAATC | 11060 |
rs562431477 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763751 | GGGCAGGTTTCATAT[C/T]TTATTTGGCTGCTAG | 11060 |
rs562443982 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767175 | GGAATTAGTCTGGCT[A/T]CCTGGGTTGGCATCC | 11060 |
rs562454532 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941349 | GGTGCCTTCCAAGCA[C/T]AGTCTCCATGCTCCC | 11060 |
rs562469698 | snp | C/T | 0 | 0 | intron-variant | WWP2 | GRCh38.p7 | 16:69820881 | AAGAGTGACTTTCTC[C/T]TCTAATTACTGAGGA | 11060 |
rs562471343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856223 | AAGCTTATGTTCTAT[A/G]TGATTCCATTTATAT | 11060 |
rs562478136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771948 | AACTAAAAGTCTTTT[C/T]AGTCTTTTTTTTTTT | 11060 |
rs562514552 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69800429 | AGCAACCAGCATGAG[G/T]GTCCTTTTTTCCTCT | 11060 |
rs562543927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894917 | CTTACATAACGGAGG[A/G]CGTTGTGTTTGGACT | 11060 |
rs562547199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862034 | TTTTGTGCCTGTTTT[A/G]TAGGAGGAAAATCAA | 11060 |
rs562578861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881618 | TGAAGACCATACTAT[A/C]TTTTCAGATTTTCTG | 11060 |
rs562598861 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69771169 | GTGATAAAAGTGATC[A/T]GGTGCTTCAGGTATT | 11060 |
rs562599350 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69762333 | GACCCGGCCCGAGTG[C/T]GGGCGGTGGAAGGCG | 11060 |
rs562616385 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819423 | CAGATCCCTCGGGCC[A/G]CAGGTCTCCCTGCTG | 11060 |
rs562617576 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940580 | TGCCTGGGTATCCAC[A/G]GGACAAAAACAGCAA | 11060 |
rs562637005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763286 | GCTTATCTTGACGAA[A/C]TGTAACTAGGTAGGG | 11060 |
rs562642042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895629 | AAAAACATCAGCTGT[G/T]TGCACCTGTGATCCT | 11060 |
rs562646786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889711 | CAGCTCTGATCATGG[C/T]TGGGGCCAGTTTTCA | 11060 |
rs562709972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69883331 | AACTTAATTTCTGCT[A/G]ACTATGAGTTGTGAT | 11060 |
rs562715547 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69894293 | ACTCTGTTGCCCATG[C/G]GGATCTCAAACTCCT | 11060 |
rs562729710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913061 | AGAATTTTTGCTCTC[A/G]TTGCCCAGGCTGGAG | 11060 |
rs562729987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69848156 | CTTAGTTAAGAAGCT[C/G]TCAGCTGGGCGCAGT | 11060 |
rs562738324 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908167 | GGAGGATTGCTTGAG[C/T]CTGGGAGGTGGAGGC | 11060 |
rs562740397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927031 | TTGAAAACAGCTCTC[A/G]AATGCTAAGTGTGGA | 11060 |
rs562740700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69856877 | TTGTGTCCACTTGGC[A/G]TATTTTTTTCCCTAT | 11060 |
rs562770751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849098 | CTAAATAGATCATCA[A/G]CTGTGTCTGCAGACA | 11060 |
rs562780800 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69889170 | ACACACACACACACA[C/G]ACACACAAATGTGGG | 11060 |
rs562784393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798997 | ATTGAGCTCATAGAG[C/T]GTTCATTATTATCTA | 11060 |
rs562818786 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836964 | GTCTCATTTTGGTTG[C/T]TTAGGTTGGAGTGCC | 11060 |
rs562838713 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828234 | TTTCTTTCCCTCCTC[C/G]TAAGGGCAGATGCCC | 11060 |
rs562853906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69841909 | GGATGTCCATATCCC[A/G]TGGTGGTGGGCAACT | 11060 |
rs562854214 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69857281 | TTGTATTTTTAGTAG[A/G]GATGGGGTTTCACCT | 11060 |
rs562858640 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823558 | ACTGCAGCCTGTGCT[C/T]CTGGGTTCAAGCGAT | 11060 |
rs562875958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933719 | CATCACCTGGGAGCC[A/G]ACAATCACACGTTTT | 11060 |
rs562943811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832997 | AAGGTGGGACCGCAG[A/G]TGCACGCCACCACGT | 11060 |
rs562949092 | snp | G/T | 9.46835e-05 | 0.00687988 | missense | WWP2 | GRCh38.p7 | 16:69939058 | ACAACGAGAAGAGGA[G/T]CCGGCTGCTGCAGTT | 11060 |
rs562956327 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69876357 | ATGTTTTTTGGGGTT[G/T]TTTTTTTTTTTCGTT | 11060 |
rs562959406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69784171 | GTGGCATGATCTCGG[C/T]GCACTGCAACCTCTG | 11060 |
rs562978907 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842603 | TCTGTTTCTGCATTG[A/G]TTTGCTTAGGATAAT | 11060 |
rs562999532 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69893809 | TCGGCCTCCCAAAAT[C/G]CTGGGATTACAGGAG | 11060 |
rs563010431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933252 | CTGGCCCCCTTGGGA[C/T]ATCCCCTTGCTGGTT | 11060 |
rs563012425 | snp | A/C/G/T | 3.31539e-05 | 0.00407137 | intron-variant | WWP2 | GRCh38.p7 | 16:69939435 | CTGCTGGTTTTAGTG[A/C/G/T]GAGGTCGGGGGGCCT | 11060 |
rs563022082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792816 | CCTATCTCAGCCTCT[C/T]GAGTAACTGGAACTA | 11060 |
rs563027402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69847684 | AAGTGCTGGGATTAC[A/G]GCTGTGAGCCACCGC | 11060 |
rs563090204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873077 | GTGTTGAAATTTGGT[A/T]AGTGACGCTGAGATA | 11060 |
rs563095948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827140 | GTCTAATGTTTAACT[A/G]AAATGGAAATTATGA | 11060 |
rs563112315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69868980 | GCGACCTCCACCTCC[C/T]GGGTTCTAAGTGATT | 11060 |
rs563117799 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766066 | TTGCCCACAATATCT[G/T]CACGTGGATTCCTAT | 11060 |
rs563137352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69824187 | GGTGCTGTGGCTGCC[A/G]GAATAGCCATGTTAA | 11060 |
rs563137398 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900385 | GTAATCCCAGCACTT[C/G/T]TGGGAGGCCGAAGCA | 11060 |
rs563146485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69833924 | CTTTCTAACTCATGC[G/T]AGGGAGGAGGCCAGG | 11060 |
rs563147890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861239 | AGCAGGTGAACACTT[A/C]CCCTCTGAACTCTCT | 11060 |
rs563165284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927661 | TTGGCCCTTAACAGG[A/G]CAGACGTGGAGGATC | 11060 |
rs563167149 | in-del | -/AGAG | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923392 | AAACCCTTTAACGAA[-/AGAG]AGCCAACATTGCATG | 11060 |
rs563185491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69834747 | TGGCCAGGCTGGTCT[C/T]AAACTCCTGACCTCA | 11060 |
rs563226444 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69880194 | GTATATAAAATGAGG[A/G]CTGGGTCTAAATTAT | 11060 |
rs563228509 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69920245 | GCAGAAAGTGTGGTG[G/T]TTGTCTTAGTAAGTT | 11060 |
rs563241975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791208 | ATTCAGCCACGCACA[C/T]TTACTTCTTTTCTTT | 11060 |
rs563265866 | snp | C/T | 1.70255e-05 | 0.00291761 | intron-variant | WWP2 | GRCh38.p7 | 16:69917904 | AGGGCAGGCGCTTGG[C/T]CCGAGGTGGGGCCGC | 11060 |
rs563283811 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898566 | GTTCCCTGATTACTA[C/T]TGAGATTGAACCTCT | 11060 |
rs563285719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868134 | TGGAAACTCCAGATT[C/T]AGGGCAAGGGGAGAA | 11060 |
rs563297980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819333 | TTCCCTATGAGCCCA[C/G]CGGCCCCCTGTGATG | 11060 |
rs563308690 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69874130 | TAGGGATTTCTGCCC[A/C]CTCCAGTGCTGAGGG | 11060 |
rs563314328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899871 | GATGAAAAACAATAT[A/G]TAATTTCTAAACAAA | 11060 |
rs563332226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817178 | ATTTCTTTGTAACTT[G/T]ATTTTTTCACCCAGT | 11060 |
rs563370846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811163 | ACATTGTTAGCAGGT[A/G]GGGTCTAATACTCCA | 11060 |
rs563378350 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775993 | TCTTTGGTTTTCCCT[A/G]AAAACTCCTTCTTAA | 11060 |
rs563383488 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850162 | GAGGCCAAGGTGGGC[A/G]GATCATGAGGTCAGG | 11060 |
rs563393855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909149 | AGAGTGCTTCTTATT[C/T]GGCAGGGCTTCGTGA | 11060 |
rs563399479 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877955 | TGGGATTATAGGCGC[A/G]TGCCACCGTGCCCAG | 11060 |
rs563426792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69926174 | ATGACTTAGGAGAGA[A/T]GATAGGCTTCATGGC | 11060 |
rs563431327 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804881 | TTCCACTTTAAATTT[A/T]AAAAACCTTTGGTAT | 11060 |
rs563432029 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69812492 | CTTTTTTTTTTTTTT[A/T]AATTGAGACAGAGTC | 11060 |
rs563463559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69816587 | AAAAACATTATTAGT[A/G]TTTTTCTGATTATTA | 11060 |
rs563465125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909763 | ATGAAAATTATGAAA[A/G]TGTTCTTATTATTAT | 11060 |
rs563521391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813022 | TGAATTCCATCCTTC[C/T]TTCTGCATTTATTAA | 11060 |
rs563521454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69805233 | TAGAGACGGGGTTTC[A/G]TCATTAAGGCCAGGC | 11060 |
rs563526354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69911182 | CACCGATTCACTTAA[C/T]CATGGCCGTCCCTGC | 11060 |
rs563537034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69900658 | CTCCTGAGTAGCTGG[A/G]ACTACAGGTGCGTGC | 11060 |
rs563591316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69911811 | AACAATAAAGGGATG[C/G]AAGAGGAGAAACAGC | 11060 |
rs563596041 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69777094 | ACAGTATATGGATAT[A/G]TATATACACATATGT | 11060 |
rs563618390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936801 | CGTCTCACGTGTGCC[C/T]GTTCTCCGTGCCTGT | 11060 |
rs563641424 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883153 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAATT | 11060 |
rs563645829 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69806581 | TTTTTTTTTCAGTTT[C/T]CCCCCCCATAATTAC | 11060 |
rs563656307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811720 | GATTGTGTCACTGCA[A/G]TCCAGTCTGGATGAC | 11060 |
rs563674267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859411 | AATACAGAAATTAGC[C/T]AGGCATGGTGGCGCA | 11060 |
rs563674323 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69831144 | GGGCTTCAGAGACTC[-/TT]AATCCTGGCGTCCTT | 11060 |
rs563679041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69937485 | GGGTAATGTCAAGTG[C/T]TAGCGAGTGGACGAT | 11060 |
rs563690168 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810201 | GGAAACTCAGCTGGC[G/T]GTTTTCTGCCTGCCT | 11060 |
rs563766871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891030 | CCAGATGGCTTCCAC[G/T]TGCTCTTCTCTAAGA | 11060 |
rs563785053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69778678 | ACAGAGTCTCGCTCT[A/G]TTGCCCAGGCTGGAG | 11060 |
rs563786801 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838653 | AGGGATGGCAAGAGG[C/T]GGCTGGGGGTTGAAA | 11060 |
rs563792642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69851546 | ATATTTCATTGTCTG[A/C]ATGTACCACAGTTTA | 11060 |
rs563805545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69766604 | GCCTCCTGACTGGTC[C/T]CAAAACCTGCCAGTG | 11060 |
rs563813341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69859488 | TGAGCCCAGGGAGGT[C/T]GAGGATGCAGTGAGC | 11060 |
rs563836653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892161 | AAACAATGATTCTCT[C/G]TTTTTTTTAATTTAA | 11060 |
rs563844494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803371 | GAACATTTACATAAA[A/C]AAAACATTATCTTAC | 11060 |
rs563849885 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69896477 | TGTGTCCGTCTTTGT[A/G]TTCCCTGTACCCAGC | 11060 |
rs563859191 | snp | A/G | 0.000799041 | 0.019972 | intron-variant | WWP2 | GRCh38.p7 | 16:69804074 | TTTTTCTCTTTTGGT[A/G]TTGAAAGAACTCTTT | 11060 |
rs563896085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69846355 | AGTAGGATGTCATAC[A/G]TAGAAAGTTGAAAAA | 11060 |
rs563898422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69886202 | ATTCTCCCTCAGTCT[C/T]CTGAGTAGCTGGGAC | 11060 |
rs563928552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916164 | AGGATTTTGACTCAA[A/G]GGCAATGGGGAGTCA | 11060 |
rs563935289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859870 | GAGCACCGCCCCCCA[C/T]CCCCGCCCCGCCCGA | 11060 |
rs563953594 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932722 | TGTCACATGCCTGGG[A/G]TCAGTAAAACTGTAA | 11060 |
rs563957156 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69824856 | GCTCACTGCAGCCTC[C/T]ACCTCCCGGGTTCAA | 11060 |
rs563972132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891680 | TCAGCCATTCCCTTG[A/G]CTGCCTCTGGGATCT | 11060 |
rs563991139 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69857687 | TTTTTTTTGAGACAG[G/T]GTTTCGCTCTGTCAC | 11060 |
rs564018810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69788424 | CCATGTGATGTGACC[C/T]TTCCCCACCCCACAT | 11060 |
rs564018811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795596 | GTGAAGAGTATACAG[C/T]ATTTATTGTTCTATT | 11060 |
rs564020196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69898682 | ATATTTATTTTTAAT[C/T]TGCAGGATTCTTTTT | 11060 |
rs564028925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884311 | ACTCCAGCCAAGGAT[G/T]GGGACAATTTTAGGA | 11060 |
rs564042642 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776948 | AATCTAAAACCCTAC[C/T]TTAGATGGGATTGTT | 11060 |
rs564044292 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69809130 | CACCAGCCGTAGCAC[A/G]TTGTGCATGTGGCTG | 11060 |
rs564049025 | in-del | -/GTTT | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69814158 | ACCAAATGTGGGGTC[-/GTTT]GTTTGTTTGTTTGTT | 11060 |
rs564077127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69878328 | GATTGAGAAATAGAC[C/T]TGCTGGATGTCAGGT | 11060 |
rs564077212 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870419 | GATCCTCCTACTTCA[A/G]CCTCTTGAGTAGCTG | 11060 |
rs564097565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850545 | GACATTACCTAGATA[A/T]GCCTGGGAGATTTGG | 11060 |
rs564111927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69930076 | CCCAGCCTCCAACCA[C/T]CAAGGTCCAGAAGGT | 11060 |
rs564124751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830552 | CAGCGGTAGTAGCCC[A/G]AAGAAGAGACTGCAA | 11060 |
rs564150146 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941291 | TCCCGGCCTGGGCCC[C/T]CAGGATTCTAGGACC | 11060 |
rs564150795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802392 | CTGAAATTCTGTCCC[A/T]TTAAACCATGACTCC | 11060 |
rs564161515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822766 | AGGAGGCAGGTGCTA[A/G]ATCAGTGCTGTCCAA | 11060 |
rs564185823 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812933 | ACTGTGTAAATGTCT[A/C]TTCCTCATCACACCT | 11060 |
rs564212279 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941740 | AACAATCAGCAGCTG[C/T]GGGTGGTGTTGTTGT | 11060 |
rs564212354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935547 | CAGACCTTTGCTAGG[C/T]CAGGAGCCAGCCGGC | 11060 |
rs564212740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934904 | GGGCGCTGCCGTTCA[C/T]GCCACGCTGCCTCCT | 11060 |
rs564217067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69842907 | CTCCTGGACTCAACC[A/G]ATTCTCCTGTCCTGG | 11060 |
rs564251357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923388 | TTAAAAACCCTTTAA[C/T]GAAAGAGAGCCAACA | 11060 |
rs564277691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69883276 | TGGTGCCCTGTCCCT[A/G]GTTGACCAGGGTGAC | 11060 |
rs564323398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844736 | TTACTGGTGAGCAAG[C/G]TACCTTCCGATAGTG | 11060 |
rs564364505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764631 | TACCATAGCTTCCTC[C/T]TCCTGGGAAAACATT | 11060 |
rs564445154 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69786531 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 11060 |
rs564455808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69929302 | TGACAAGTGTGAGTG[A/T]GCTTGGCTTTGGCTG | 11060 |
rs564461936 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69826676 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 11060 |
rs564468888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921695 | CCCACTGAAGATGCC[C/T]GGCACAGCCTTGCAC | 11060 |
rs564470350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69913900 | CATGGTGAAACCCCC[A/G]TCTCTACTAAAAATA | 11060 |
rs564474559 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69787375 | AGGAGGATCCCTTAA[A/G]CCCAGAGTTTCAAGA | 11060 |
rs564481838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828233 | CTTTCTTTCCCTCCT[C/G]CTAAGGGCAGATGCC | 11060 |
rs564515918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779631 | AGAGTCAGGACCAAA[A/G]GCTCAAAACTGCTAC | 11060 |
rs564526669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820254 | TTTTTGTTATTATTA[C/T]TTTTTTGAGATGGAG | 11060 |
rs564536437 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882367 | TTTCTTTTCTTTTCC[C/G]TTTGAAACTCACCTA | 11060 |
rs564549694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793461 | CAGAGTTATCACTCA[C/G]ATCAGTCTTCCTGGA | 11060 |
rs564583094 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810143 | AGAATTCGTTCTTTC[A/T]TTTGCTCCCTTGTTT | 11060 |
rs564595572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920184 | TGGATTGCTCATTGT[A/C]CAGGGAGGAAACCAT | 11060 |
rs564603989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920888 | ATGTTGGTGTGTGAA[A/C]GGGAAGATTCCCAGA | 11060 |
rs564660422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822065 | AGAGACAGGGTCTCC[A/C]TTTGTTGCCTGAGCT | 11060 |
rs564677364 | in-del | -/A | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837818 | CCTGGAAACAAGATG[-/A]AAGGACAGTTTGTCT | 11060 |
rs564686948 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940704 | GCTGGCACCCCAGGT[A/G]TTCTGAGACCTTGAG | 11060 |
rs564702718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857142 | AGAGTCTCACTCTGT[C/T]GCTCAGGCTGGAGTG | 11060 |
rs564704407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907366 | TATGCTCACATCGTC[C/T]GCTTCTATATCAATA | 11060 |
rs564731293 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69808667 | TCGGCCTCCCAAAGT[G/T]TTGGGATTACAGGCG | 11060 |
rs564746595 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914491 | TGCCGGGCACAGTGG[C/T]TCAAACGTCTAATCC | 11060 |
rs564749497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69849075 | AGCCTAACCGTCTCC[A/G]GTGAGCTCTAAATAG | 11060 |
rs564762164 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795948 | CCACCATGCCCTGCT[G/T]CAAAATAAGAGTACT | 11060 |
rs564795495 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928564 | GTATTTGTTCCCCAG[A/C]CCCACTCCATGAACA | 11060 |
rs564822905 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936688 | GTGGGAGACTTCAAG[A/C]CTGCAGCGTGGAATT | 11060 |
rs564824481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908114 | GCTGGGCATCGTAAT[A/G]TGTGCCTGTAGTCCC | 11060 |
rs564840785 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771108 | GTGGTTCAGCTTATT[A/C]GCCTCCAGAAGATTG | 11060 |
rs564853938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814186 | GTTTGTTTTTGACAA[A/G]GTCTTGCTCTGTCGT | 11060 |
rs564869819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69861351 | GTCACCATTTACTAT[A/G]CCTTCTCTCTCAAGG | 11060 |
rs564899424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861980 | AATACCGCTTACCCG[A/G]ATTGGAATGTGAGAG | 11060 |
rs564943559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901508 | AGCTCTGCCTCCCGG[G/T]TTCATGCCATTCTCC | 11060 |
rs564950065 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | WWP2 | GRCh38.p7 | 16:69920816 | AAATAAAATGCATTA[A/C]AGCAATTTTTTTTTC | 11060 |
rs564950401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868313 | CGCTATCATTAGTGG[A/T]TAAGTGTTTCTGAAA | 11060 |
rs564952271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69875623 | TTTCAACAGTGTTCA[C/T]AGCATTTTCACTAGA | 11060 |
rs564990952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69769177 | AAAAAACTAGTCAGG[C/T]GTGGTGACAGGCACC | 11060 |
rs564991797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777717 | CAAGATTTATGTAGA[G/T]GATAAGTTCAGAGGA | 11060 |
rs565011776 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793814 | ACTATACCTACCTCT[C/T]ATTAGAATTCAAGCC | 11060 |
rs565012404 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942138 | TTTCACAAGTTCCAC[A/G]ACGGTCGAGGGACTC | 11060 |
rs565039023 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894978 | CCATGCTTTTTCTCC[C/T]GCAGCCATTGGCTGC | 11060 |
rs565065326 | snp | A/C/T | 3.29507e-05 | 0.00405887 | missense | WWP2 | GRCh38.p7 | 16:69934103 | CACCTCACCTACTTT[A/C/T]GCTTTATAGGCAGAT | 11060 |
rs565076081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933848 | GCTTGTCACAGGGCT[C/T]GACTCCCTGGGACAC | 11060 |
rs565077756 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761787 | CCCCACAAAGGCTGA[A/G]ATGTTTGTGGTCCTG | 11060 |
rs565100928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69792108 | TGAAGAAAGCTGATA[A/G]TGTAACCTGTGGGGT | 11060 |
rs565105513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69889065 | TGCCAATCAATTCCA[C/T]TGCTTTGGGAGGCTG | 11060 |
rs565132369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919461 | TGTGAACCACCATGC[C/G]TGGCCCACATTTAAA | 11060 |
rs565136811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763231 | CTTTTCTCTTTCTTC[C/T]GTTTAAATTATTCAG | 11060 |
rs565147677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853905 | TCTCCCATGGTGGTC[A/G]GCTTTGGTGTTCAGC | 11060 |
rs565152091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855045 | AATTTTTTGTAGAGA[G/T]AAGGTCTCCCCAGGC | 11060 |
rs565163481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887108 | TTGTGAACGTAAGTG[A/T]TCATCAAAGAGGTGA | 11060 |
rs565172568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805746 | CTCTGGAGTAGCTGG[A/G]ACTATAGGTGTGTTA | 11060 |
rs565187617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894422 | GATGAGACTTTGGCC[A/G]TATGTGGTTACACAC | 11060 |
rs565207882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917053 | ACAAAACCAAAGACC[A/G]TGCAACATGTTTACA | 11060 |
rs565215671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798557 | AGTTTTTAGAATCAA[A/G]ACAAAACAAAATGTA | 11060 |
rs565227109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763767 | TTATTTGGCTGCTAG[A/C]CTAGTGCCTGGCATG | 11060 |
rs565234311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805132 | GCAATCTCCACCTCC[G/T]GGGTTCAAGCGATTC | 11060 |
rs565290770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872034 | CAGAATAGAGGGTGG[A/G]CGTCAGAAGGCTCTA | 11060 |
rs565291290 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891032 | AGATGGCTTCCACGT[G/T]CTCTTCTCTAAGATG | 11060 |
rs565291517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846943 | CTGTCACCCTGGCTA[C/G]AGTGCAGTGGCTCAC | 11060 |
rs565309069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774682 | TGCCTTTTTAATTTC[C/T]ATTTTGGCCAGGTGC | 11060 |
rs565349753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775308 | AATCTTTCATAGGCT[C/T]TATGACCTGCTTTAT | 11060 |
rs565355683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882012 | TTTTGTATAGATGGG[G/T]TTTTGCCATGTTGAC | 11060 |
rs565369527 | in-del | -/CAA | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760431 | CCTCCCGGGTTCAAG[-/CAA]TTCTCCTGCCTCAGG | 11060 |
rs565383480 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762887 | CCGAGACTTTGATGA[C/T]GGTCCCATTCAGTTT | 11060 |
rs565430040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69871245 | GCTATGATCGTGCCA[C/T]TCCAGCCTGGGCAGC | 11060 |
rs565433749 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69881524 | CTGGAGTTTAGTTAA[C/T]AGTAGTATACTAATT | 11060 |
rs565523200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898172 | AGCTGGGATTACAGG[C/T]ATCTACCACCATGCT | 11060 |
rs565530211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841054 | TGCTTGGAGAAAAAC[A/G]TGTGTCATTCACTCA | 11060 |
rs565534411 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852437 | CCACCACGCCCAGCT[A/G]ATTTTTTTGTATTTT | 11060 |
rs565540316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909330 | AAAGGGGATGTATTC[C/T]GCTCCAAGAAAGAAT | 11060 |
rs565542874 | snp | A/G | 4.97946e-05 | 0.00498947 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933082 | GGCCGCGCCCTGTGT[A/G]TGTCTCTCTCTGTGT | 11060 |
rs565545218 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868206 | GTGGTGGCTGGCCAC[A/G]GGCAGGGAGGTGGCA | 11060 |
rs565563671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887631 | GGTGGATCTCGAACT[C/T]CTGACCTCAAGTGAT | 11060 |
rs565578492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891884 | GTCATACATCTTTCC[C/G]CTGACCCTGACATCC | 11060 |
rs565624010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781774 | ATTTGAGTCTGGGAA[A/G]TCTAAGGTGGAGGGC | 11060 |
rs565635024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766905 | ATTACAGGCATCTGC[C/T]ACTATGTCCAACTAA | 11060 |
rs565648521 | in-del | -/AACAACAACAACAACAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783788 | TGTTTCTACAACAAC[-/AACAACAACAACAACAAA]AACAACAACAACAAC | 11060 |
rs565655096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822977 | CTCCATCTTTACTAA[A/G]AGTACAAAAATTAGC | 11060 |
rs565674208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767950 | TCAAGTGATCCTCCC[A/G]TCTTAGCCTTCCAAG | 11060 |
rs565687589 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829247 | CTCCTGTCTGCTCTG[C/T]CTGTTTCTGTCCTTC | 11060 |
rs565719215 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825285 | CAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT | 11060 |
rs565744102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789252 | TTTGTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 11060 |
rs565754536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69915681 | GTCAGCAATGGGGCA[A/G]GAGACCATCGTTTTT | 11060 |
rs565756196 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941405 | GGAGGTGCAGCCTGC[A/G]TCTGCCTCTGTCGTG | 11060 |
rs565796100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904381 | GTGCGCATTTTCTTT[C/T]TTTTTTTTTTTGAGT | 11060 |
rs565814418 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69858908 | GGAATGCTGCTCCTT[C/T]GACATGGGCACTGGA | 11060 |
rs565830835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69897302 | GAGATGGGGTTTTGC[C/T]GTGTTGCTCAGGCTG | 11060 |
rs565841043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69810600 | GCCTGGCTAATTTTT[C/T]GTATTTTTTTTTAGT | 11060 |
rs565864306 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803586 | CCACCCTGCTTTTTT[G/T]TGTGTGTGTGTGAAA | 11060 |
rs565883319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69851854 | TGGGCGTGGTAGTGC[A/G]CTCCTGGAGTCCCAG | 11060 |
rs565890022 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760306 | TTTGGAGTGGTACTA[C/T]AAAAAGTAGAGACTA | 11060 |
rs565902093 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923986 | TCAACGTGATTTGTG[A/T]TGGAGAATTTTAGGC | 11060 |
rs565929664 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897410 | GCCCGGCACCTGAGG[A/T]GGTCTTTTTTTAACC | 11060 |
rs565988524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69904903 | CAAGAGGCCGTTAGC[C/T]TGAAGCTGTCTCCAT | 11060 |
rs565997536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908354 | CTATGAAACCCAGAA[A/C]TTGCAATACAAATTT | 11060 |
rs566062939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903495 | GAAAAATGGCCGGGC[A/G]CAGTGGCTCACACCT | 11060 |
rs566082332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799807 | TACTGGATGTTGGAA[C/T]GTGATGGACGCGCCA | 11060 |
rs566084875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69935275 | GGCCGGCCCTTCCCA[C/T]CGTCGAGGAGTTCTT | 11060 |
rs566127720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814653 | AAACAACCTCCTATT[C/T]ATTTAAAAATCTTTT | 11060 |
rs566138919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928881 | TTAGAACAAGACTTA[A/G]CCTGTAAGTGGGAGA | 11060 |
rs566155722 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837751 | CCCTCAGCACGCTTC[C/G]AATAGCGGTGTGTGT | 11060 |
rs566162371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764229 | TTTTGAGACAGGATC[A/T]TACTCTGTTGCCCAG | 11060 |
rs566169320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793713 | TAGGTTCTGCAATAG[C/T]GATGTTATCTATGGG | 11060 |
rs566182090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788600 | GCGTTTTCTCAAAAG[C/G]CACCCTCTTCCTGAT | 11060 |
rs566189071 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844487 | TAACTTAATTTGGGG[A/C]TCAAAGTCAGATTCA | 11060 |
rs566199608 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69903000 | ACATTTAATCTGAGC[A/C]GGGGTCCAACTGCAA | 11060 |
rs566202229 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811222 | GCTCTCCCAGGAGCA[C/T]TGCAGACTTTGGCTT | 11060 |
rs566242950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69799371 | ATCAACCTGGTATTG[C/G]AATTTCCCCCAGGAC | 11060 |
rs566290302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930357 | GTGGCCCCTGTGGTG[C/T]GTTCTACTGCCCTTA | 11060 |
rs566306959 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69821153 | AGCGGTCTCTGAAAA[C/G]CCCTCTGTGTGTCGC | 11060 |
rs566310952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829093 | CAGGAGCCGTCTTCG[A/G]TACCCGACCCCTCTT | 11060 |
rs566312733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69889292 | ATCACACCACTGTAC[C/T]CCAGCCTGGACTATG | 11060 |
rs566325589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910320 | AATTGTGTCACAAAT[A/T]AAACATTGACTTTAA | 11060 |
rs566391120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794757 | GTTGCCTTGGCAAAG[C/T]TGCTGGGATTATAAA | 11060 |
rs566398654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921363 | ACTAGACTAGCTAGC[G/T]GCCTCCCCTCCTCCT | 11060 |
rs566403432 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767901 | GAAGTACAGTGGCAT[A/G]ATCATGGCTCACTGC | 11060 |
rs566414368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793160 | GTTCAAGACCAGCCT[C/T]GCCAAGATGGTGAAA | 11060 |
rs566430901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69882471 | AATGTTAAGCATTAC[A/G]GACAATGTAAAGCAT | 11060 |
rs566462088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69908641 | CATTGGGTCGGCCTC[A/G]CATGTCATCTTTGAT | 11060 |
rs566477195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835319 | CTTTCAGCCTCCCCT[A/G]TATGCTCGAATCTGT | 11060 |
rs566483444 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931649 | CCCATCTCCTATCGC[A/G]TGGCCTGTTAAACCC | 11060 |
rs566491205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934529 | AACATTAAATATGTG[C/T]TCTGTTGAGGGCCTT | 11060 |
rs566501471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875249 | ATTATGTCTAAAAAA[C/T]GTATACACTTTAATT | 11060 |
rs566510897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786247 | CCTCCCGGGTTCAAG[A/C]AATTCTCTGCCTCAC | 11060 |
rs566510928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69893745 | GCCAGGGTTTCACCA[C/T]GTTGGCCAGGCTGTG | 11060 |
rs566522600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779863 | GCATTATTCAAGATA[C/T]GATCTTTTGCTTCCC | 11060 |
rs566543964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915009 | AATCTCCCAGGAGGA[A/G]GAGAAGGGAAGGCAA | 11060 |
rs566548883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857718 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCACAGC | 11060 |
rs566553943 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816701 | TATACATATACACAC[A/G]TATACATGTACACAT | 11060 |
rs566609661 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69842543 | GTTCATGTGTACTCA[A/G]TGTTTAGCTCCCACT | 11060 |
rs566618812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849172 | AGTCCACTGTGAACA[C/T]TTCAGGAAGTCCTGG | 11060 |
rs566632398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881712 | ATTTTTTATTTTTTA[G/T]ATAGAGCCTCACTCT | 11060 |
rs566642754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69877190 | TCGTGTGGCCAACCC[C/T]GTCAATGATCTTAGC | 11060 |
rs566658065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69907935 | GCTCGGAGGAGAGGG[A/G]TAGTCATAGAACCTG | 11060 |
rs566675570 | snp | G/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760872 | ATCTGAGCACTTTGG[G/T]AGGCCAAGGCAGGTG | 11060 |
rs566682844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69772690 | CATTACCATGGCATT[A/G]GCACACTGTCATGGC | 11060 |
rs566710941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806516 | GCAAAGAGCTCACCC[A/G]TAAAACCAACTGGGT | 11060 |
rs566766241 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836471 | GCCTTGCTTTGCTCT[C/T]AGTGACAGTAAATTA | 11060 |
rs566768577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69894662 | AAGGGGCTAGTGAGA[C/T]AGTGGTTCAGGCCGT | 11060 |
rs566806690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841956 | GTTCTGTTCCTGGCC[A/G]TCAAATCTCAAACAC | 11060 |
rs566813532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770623 | TAAGAACCTCGATTT[A/G]TAGCCGGTTGGTCAG | 11060 |
rs566848334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771253 | GTTCTGTAATAATTA[C/T]TATTTTTCTTTTTGA | 11060 |
rs566866988 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904109 | TATCCTTAAGCCAAA[C/T]ATCTTTCTCAGGACT | 11060 |
rs566879092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69906221 | GGGACTACAGGTGCC[C/T]GCCACCATGCCCAGC | 11060 |
rs566883938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860178 | AAAAAATTAGCCAGG[C/T]GTGGTGGTCCGATTC | 11060 |
rs566890449 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875695 | TAAGACACAACTCCT[A/G]ATCTATTCCAGTCTT | 11060 |
rs566890795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868522 | CTGCAGCTCCCTGAG[G/T]GGTCCAGCTTGCTCC | 11060 |
rs566913489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69862096 | TTGAGACAGACTTTC[A/G]CTCTTGTTGCCCCGG | 11060 |
rs566918653 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779310 | ATTCCAAATGCCTAC[-/A]ATTATATAATGTCAG | 11060 |
rs566941267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69813877 | ATATATTTTTGTCCC[A/G]ACATAATCCAATATA | 11060 |
rs566990017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69824479 | GTAAGGCACACACTT[C/T]TCAGAAAATAATATC | 11060 |
rs567002690 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903459 | GATAAGATGAAAGTT[A/G]AAAGAATTTTTGGAA | 11060 |
rs567003281 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926669 | TGGAGAGATCATTTA[G/T]TGAAGCTTCCACACA | 11060 |
rs567003541 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901778 | GTGTATCAATTTATA[A/G]GGGCCACTTGAAAAG | 11060 |
rs567012471 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69913165 | AAGTAGTTGGGGTTA[C/T]AGGCACATGCCACCA | 11060 |
rs567073560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907156 | GGTGCATGGAGGGCT[A/G]TCTGAAATCAGATGG | 11060 |
rs567074768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939669 | CAGCTGTCCTGGCCC[C/T]TCCCTTAACACCCCA | 11060 |
rs567094943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855477 | TAATGCAGAATCCCA[A/G]AGTGTTCCTTTTTTC | 11060 |
rs567102900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69866049 | CGAGGTGTCTCTGAC[C/T]TCGCATCTCATCATG | 11060 |
rs567137958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69882643 | TGCTTTCCCTGGGCC[A/G]CAGGGGTCGGGAGGG | 11060 |
rs567169116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880935 | TTGGAACACACAGTG[A/G]ACTGGCAGTGTCTCT | 11060 |
rs567175672 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WWP2 | GRCh38.p7 | 16:69820463 | TGGCCAGGCTGGTCT[C/T]GAAATCCTGATCTTA | 11060 |
rs567180336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69762790 | AAAATGGGTTTATGG[C/T]GTGGAGCCAGAGGGA | 11060 |
rs567184902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812577 | TCTATCTCCTGGGCT[C/T]GAGGAATCCTCCCAC | 11060 |
rs567243701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69812107 | CTGCATCAGTTCCTT[A/G]GGGTATTTATGTCTT | 11060 |
rs567253174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69899081 | ATTTGCTCCCAGTCT[A/G]TGGCTTGTCTTTTCA | 11060 |
rs567258685 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916736 | CTGTGGCATTCAATT[A/G]AATGAAGGGTGACAG | 11060 |
rs567296530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804587 | TATGCTATTGTAAAA[A/T]TATGTTTTAATATCT | 11060 |
rs567311892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910631 | GGCCAGGCTGGTCTT[A/G]AACTCTTGACCTTGT | 11060 |
rs567322345 | in-del | -/T | 0.00159681 | 0.0282109 | intron-variant | WWP2 | GRCh38.p7 | 16:69804075 | TTTTCTCTTTTGGTA[-/T]TGAAAGAACTCTTTA | 11060 |
rs567329547 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850611 | AGTTTGCCAGACCGA[C/T]GAAGTGGGGTTCAGG | 11060 |
rs567331277 | snp | A/G | 4.94621e-05 | 0.00497279 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931576 | TCGAAGATTCCTTCC[A/G]ACAGGTTAGATCATG | 11060 |
rs567358549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69817997 | GGCGTGTTTCAAGTT[C/T]TTGATGCCTGCTGCC | 11060 |
rs567359720 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927228 | TGCCCCAGGGCTGTG[G/T]CTGGGGCCGGCTCCC | 11060 |
rs567367443 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866054 | TGTCTCTGACCTCGC[A/C]TCTCATCATGGCTGG | 11060 |
rs567381191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768927 | CAATGCTGGACAGAG[A/G]AAGGAGGCCAAGAAA | 11060 |
rs567394704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887932 | GCCCAATACATGTAG[C/T]GTAACATTGTAGATA | 11060 |
rs567404963 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762039 | TCAATTAAGTATTTG[C/G]TGACTTAACAGTCTG | 11060 |
rs567433650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846588 | TAGCTTGGCATGGTG[A/G]CGTGCACCTGTAATC | 11060 |
rs567445561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69902333 | CATGGTTCATATACA[A/G]CTGAACCAAGGGCAG | 11060 |
rs567470348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69841144 | GCCAGATGGCAGTGG[G/T]CCAAATTCACATGGT | 11060 |
rs567480342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926574 | AGAGGTTGTGTCAAC[C/T]CTGTTATACCTGCAG | 11060 |
rs567488806 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | WWP2 | GRCh38.p7 | 16:69845649 | CTGTGAAAGGGTTTT[A/T]TCTGAGGGGTTCATT | 11060 |
rs567500291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69832468 | CTCAATGGTAATCAT[C/T]TAATATTTTGAACTA | 11060 |
rs567503172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791744 | AGGCTGGTTTCAAAC[A/T]CCTGGACTCAAGCAG | 11060 |
rs567533666 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872974 | ATCTTTAGAGACTGC[G/T]GGTCGTTTGGTAGTT | 11060 |
rs567571044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893449 | GCTATGACAGCAATA[G/T]TGCATTTTCTTCCCA | 11060 |
rs567589495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805307 | TCCCAAAGTGCTGGG[A/T]TTACAGACGTGAGTC | 11060 |
rs567592585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925062 | TGGCCGCCTTGAGCC[A/G]GAGCTGAGCGGAGGC | 11060 |
rs567602368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789374 | AGCTGGGACTACAGG[C/T]GTGTGCCACCGCGCC | 11060 |
rs567645942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69885001 | ACTTGCCTATTCATA[C/T]ATCAGTACCACATTG | 11060 |
rs567661763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831932 | CTCCTGGGCACAAGC[A/G]ATTATTCCGCCTCAG | 11060 |
rs567679847 | in-del | -/TT | 0.0741063 | 0.177655 | intron-variant | WWP2 | GRCh38.p7 | 16:69893570 | TTTTTTGTTTGTTTG[-/TT]TTTGTTTTTGTTTTT | 11060 |
rs567684521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781076 | TCAGAACTTATTAAC[A/G]TTAGTGTCACTAAAG | 11060 |
rs567728569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872673 | CAGATGATGGCACCA[C/G]TGGTGAATGGGTTGA | 11060 |
rs567746511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850975 | CATCATTGTCACTCA[A/G]AGTCCAAAATGTATA | 11060 |
rs567755171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910112 | AATTTGCTAACTCCC[A/G]ATCTGTAACCCCCAA | 11060 |
rs567765530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69898069 | CTTGCTCTGTTGCCC[A/G]GGCTGGAGTGTGCAG | 11060 |
rs567785994 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937048 | CGCGGTAACGGCCAC[A/G]CGGCCTGGCCGGGAG | 11060 |
rs567797483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936812 | TGCCCGTTCTCCGTG[A/C]CTGTTCCTCAGGCCT | 11060 |
rs567829345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880258 | TTAAGTAAACAGTGT[C/T]ATTTTTTACTGTGAT | 11060 |
rs567844544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69917975 | GACCTGCTTAGTGAG[C/T]AGGGAAAACAGCGTC | 11060 |
rs567879539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873107 | AGTTTTCTAGTGCTC[A/G]TGACAGCAGAGGTGT | 11060 |
rs567903879 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839485 | TACAGTCACCCACAG[G/T]ACTGAATCTGCCTGG | 11060 |
rs567911226 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69809703 | AACCCAGGAGGCAGA[A/G]GTTGCAGTGAGCCGA | 11060 |
rs567934067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790041 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 11060 |
rs567949867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69810528 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 11060 |
rs567967116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69879539 | CATCCATGTTGTAGC[A/G]TGTGTCAGAATTTCC | 11060 |
rs567980667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908966 | AGTGACGTTTATTCC[A/G]GGTCACTTGATTGCT | 11060 |
rs567998638 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761281 | CCATCTCTTAAAAAA[A/T]ATATTTCTCTGCCAG | 11060 |
rs568000661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69871142 | ATAAAAAAATGAGCC[A/G]GGCGTGGTGCTGTGT | 11060 |
rs568006973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774499 | TGGATTCAAGTGATC[C/T]ACCTGACTTGGCCTC | 11060 |
rs568028515 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854074 | CCACAATAAGGGCAC[A/C]ATTCAGGGCACGTGA | 11060 |
rs568042797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775214 | TTTGTTTTCAGAGAA[A/G]GATATTTCTTTCCTT | 11060 |
rs568043021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69903637 | GCCAGGTGTGGTGGC[A/G]CATACCTGTAGTCCC | 11060 |
rs568091562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792134 | GGGGTGTGACTGCGC[A/G]GTTTCCAGTTCCCTT | 11060 |
rs568101014 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804416 | TTTTCCCTAATATGT[A/G]GCTGATTGGTTTAGC | 11060 |
rs568103510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69922678 | TTTGGCTTTTGGTTT[C/T]CTGGCCATGATGCAT | 11060 |
rs568119247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69921943 | GCTGGGCGTGGTGGC[A/G]GGCACCTTTAGTCCC | 11060 |
rs568119306 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837012 | CACTGCAGCCTCGAC[C/T]TCCCGGGCTCAGGTG | 11060 |
rs568135299 | snp | C/T | 0.000380584 | 0.0137894 | intron-variant | WWP2 | GRCh38.p7 | 16:69930103 | AGGTGGGGCCAGCCC[C/T]TCACCCTTTTCTTCC | 11060 |
rs568136472 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69863539 | AGCTACAAGGGAGGC[C/T]GAGGCAGGAGAATTG | 11060 |
rs568138281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856413 | TTGGTAAAACTTGCC[A/G]AATTGTACCCTTAGA | 11060 |
rs568138895 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788767 | AGATCCACAGTAAGA[A/G]ATTTTTGTCGCTTTG | 11060 |
rs568142709 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774594 | AATGTTTTGCAGATA[-/CT]CTCAGTTTCTTCCTT | 11060 |
rs568185348 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941973 | TCACCGTACCCTTTC[A/G]GCACCCTCTGCCTCC | 11060 |
rs568187447 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904673 | ACTGTACCTGGCCCT[A/G]GTGTGCATTTTCATC | 11060 |
rs568204660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829332 | GGCTGATCTTGTCAC[A/G]CCTCAGTTAAAAAAC | 11060 |
rs568204821 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837631 | TCCTGTTGAACATTA[C/T]CAGTCCTCCAGGAAG | 11060 |
rs568218717 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69857938 | TAGGCGTAAGCTACC[A/G]CATCCGGCCTAACAG | 11060 |
rs568233255 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800687 | CTACCACCTCAGCCT[A/C]CCAAGTAGCTGGGAT | 11060 |
rs568236303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822331 | TTCGTGCAGTAAGCA[C/T]CTTTGAATTCCGAGC | 11060 |
rs568242081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816632 | TTACTAAAAAGGACA[A/G]TATTCTGAGTGCTTC | 11060 |
rs568258970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69864638 | CACTGCCACCTTGGC[C/T]TCTCGGGGTTCAAGC | 11060 |
rs568293919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766104 | TTTATAATCAACATC[A/C]ACAAAATTGAGCCCT | 11060 |
rs568311188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916340 | GCTGGGACCAAGGGC[A/G]CACACTCCACCACCC | 11060 |
rs568317006 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807831 | AGGTGTGGTGTTGCA[C/T]ACCTGTAGTCCCAGC | 11060 |
rs568343453 | snp | A/G | 3.71568e-05 | 0.0043101 | missense | WWP2 | GRCh38.p7 | 16:69871923 | ACAGTGGCTTGGCCA[A/G]TGGCACAGGTGAGTG | 11060 |
rs568351696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69822875 | GGCACCGTGGCTCAC[A/G]CCTGCAATCCCAGCA | 11060 |
rs568358635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814478 | CAAATTCCTTCACAT[C/G]TGTAATGCACAGAAG | 11060 |
rs568360738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883636 | CATCGGTTAAACATG[C/T]GCCATGGTGGTTTAC | 11060 |
rs568378754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764192 | ATTTATTGACACAAT[A/G]GAAAATTTTATTTTT | 11060 |
rs568428122 | in-del | -/GA | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69901443 | CTGAGATGGAGTCTT[-/GA]GCTCTGTCGCCCAGT | 11060 |
rs568450630 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899495 | AGCACTTCGCGAGGC[C/T]GAGGCAGGTGGATCA | 11060 |
rs568456298 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69902516 | AGCAATGTGTTGGGT[A/G]GGGACTGAAAACAAG | 11060 |
rs568461184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869493 | GGACCACAGGGGCAC[A/G]CCACCACACCTGGCT | 11060 |
rs568465895 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940361 | TTCGGGACTGAGAGC[A/G]CCAAGGGTCTTTGCC | 11060 |
rs568466844 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933504 | GTTGCTGTGTATTTA[A/C/T]GTTATGTTGCCCGCC | 11060 |
rs568474544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815269 | TGGCCTCCCAAAGTG[C/T]TGGGATTACGGGCGT | 11060 |
rs568476712 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69816218 | CCCTAAATTGAACAT[G/T]ATTATTAATATTTTG | 11060 |
rs568489382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69772583 | TAGCAGCTCAGGGGC[A/T]GTTTTGCTGTCATAT | 11060 |
rs568496812 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828430 | GGAGTACAACAGCGC[A/G]ATCTCAGCTCACCAC | 11060 |
rs568503402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808007 | ACAACTTGAATATGT[A/G]CATGTGTCCACAGCT | 11060 |
rs568512801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69820724 | TATTTTTCTCATTCA[C/T]TGTCCTCCACAAATA | 11060 |
rs568526646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69933864 | GACTCCCTGGGACAC[A/G]TGTCCCCATACTAAC | 11060 |
rs568544788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890094 | CAAGTAGCTGGGACT[A/G]CAGGCGTGCACCACC | 11060 |
rs568569436 | in-del | -/AC | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69820823 | CATGAATACATGCAT[-/AC]ATACACACACACACA | 11060 |
rs568609510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794670 | AATTTTGCAAAGGCA[A/G]TTTCACAATTAGAAA | 11060 |
rs568611630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69789298 | GCAGTGGTGCGATCT[C/T]GACTCACTGTAACCT | 11060 |
rs568630365 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787725 | CAATAGAAGATCACT[C/T]CTCTGGGCTTTACCT | 11060 |
rs568630763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806433 | CTAATTTTATAAAGT[A/G]AATTGATGTGCTTTC | 11060 |
rs568631918 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69800807 | TGACCTCAGGTGATC[C/T]GCCCGCCTCATCCTC | 11060 |
rs568661668 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821741 | TTTTTTTTTTTTTTT[-/TT]GTAGAGATGTAGTCT | 11060 |
rs568676393 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895928 | TGCTTAGTATGGTTA[A/C/G]TTTGTGACTCTGCAG | 11060 |
rs568681071 | snp | A/G | 0.00196297 | 0.0312671 | intron-variant | WWP2 | GRCh38.p7 | 16:69929552 | CTTGGGCTGAGAGGG[A/G]GGCCGGGCTGGGCTG | 11060 |
rs568681306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935571 | AGCCGGCCAGCGTGC[A/G]GGGCAGATGCGGGCC | 11060 |
rs568694240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835888 | GCTCCCTGCAATCTC[C/T]GCCTGCCGTGTTTAA | 11060 |
rs568694632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827636 | AAAGGAGGTTTGTTC[C/T]TTGGAAGGTGTTTAT | 11060 |
rs568700986 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842301 | TAGGATCCTTATTTA[-/T]TTTTTTTTTAATTGA | 11060 |
rs568705080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849882 | TCAATTAAAATGATA[C/T]ATGGTACCTTATTAT | 11060 |
rs568711071 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69939532 | TTTTGCGTGGCCCTG[C/G]GGTGTTGGGTTGGAG | 11060 |
rs568732607 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69785787 | ACCCACTACCACGCC[A/C/T]GACAAATTTGTTGTT | 11060 |
rs568765383 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69848335 | CATGCCTGTAATCCC[A/G]GCTACGTGGGGAGCT | 11060 |
rs568770885 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923186 | TGAGCCACGGCACCC[A/G]GCCGCCATGACTCCA | 11060 |
rs568788685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928053 | AATTTCAGTCGAGTC[A/T]TAGATACCAGGTAAG | 11060 |
rs568810348 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816341 | TAATTTCAGCACTTT[A/G]GAGACTGAGGTGAGA | 11060 |
rs568819638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935209 | CTGAGTGTCCCACCC[A/G]GCTCCCCTCTTAGGA | 11060 |
rs568821636 | in-del | -/A | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933457 | CTGAAGGCAGCATGG[-/A]TTACATTGTCATGGA | 11060 |
rs568829207 | in-del | -/CCGAGTAG | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69883871 | CATAAACAGTCAGAT[-/CCGAGTAG]CCGAGTAGTGTTGAT | 11060 |
rs568858263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69835167 | CAAAGGCAGCAGGAA[C/G]ACATACTGGAAGAGA | 11060 |
rs568873857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901563 | GACTACAGGCATGTA[C/T]CACCACGCCCAGCTA | 11060 |
rs568879098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784010 | TCAGTTCTCAAGTGT[A/G]GTCCTCAGACATTGG | 11060 |
rs568889440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900928 | TGCCATCCTGTGTTT[C/G]GAGGCATAAAGTGCT | 11060 |
rs568898134 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931702 | TGAGTCTTGGTGACT[C/G]TGTCTGCTGGATATT | 11060 |
rs568919835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888588 | TAGAAAACAGCTTTT[A/C]TCTCTTGAATTTTAT | 11060 |
rs568926084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69762696 | CTTAGGTTCCCAGGC[A/G]TGGAGAGGAGCGATC | 11060 |
rs568949535 | in-del | -/T | 0.220843 | 0.248294 | intron-variant | WWP2 | GRCh38.p7 | 16:69922896 | TTTTTGCCACGACTC[-/T]TTTTTTTTTTTGAGA | 11060 |
rs568949773 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69894114 | GGAGTCTCGCTCTGT[C/T]ACCCAGGCTGGAGTG | 11060 |
rs568976560 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69847907 | ACTGCATCCAAACCA[C/T]AGCAGGGAGTCAAGT | 11060 |
rs568993491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69876493 | CCTCAGCCTCCAAAG[C/T]AGCTGGGATTACAGG | 11060 |
rs569009090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876043 | CACTGCTGCAACCTC[C/T]GCCTCCTGGGTTAAA | 11060 |
rs569022816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69887169 | TAGTGTGTTTCACTT[C/T]TGTCTCATTGTCTAT | 11060 |
rs569025828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69842473 | AGTTTTTCAATTCTT[A/G]CTCCTCTCCCTCCTT | 11060 |
rs569076204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779019 | CAATGGTGCAATCTT[A/G]GCTCACTGCAACCTC | 11060 |
rs569078090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786671 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 11060 |
rs569093580 | in-del | -/TTTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912568 | AAATTGGAGGGTAGT[-/TTTG]TTTGTTTGTTTGTTT | 11060 |
rs569145219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813225 | TGGAGTGCAATGGCG[C/T]GATCTTCGCTCACCG | 11060 |
rs569169964 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890284 | TGCGCCACGCTACCT[A/G]ACTCCCGTCTGTTCA | 11060 |
rs569172224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920403 | GCATGTTTCAGAATT[A/G]GATGGAATCTGGTCT | 11060 |
rs569177613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69911475 | GAAAGGATGTGTTTG[A/G]GGAAGGATGCATGGG | 11060 |
rs569219397 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69847108 | TTTTAAATTTGAGAT[A/G]GAGTCTTGCTCTGTC | 11060 |
rs569234958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798209 | AAGTGTTCGTATCCT[G/T]TGGAGGAATACTCAA | 11060 |
rs569235591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69918781 | TGCATCCATTTACTG[G/T]CTCAAAACCTTTTGT | 11060 |
rs569241465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69912037 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 11060 |
rs569250669 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870299 | TTTATTTATTTATCC[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs569258761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69833289 | AAGAAACTGGACAGC[A/G]TGTCCTTTACAGTTT | 11060 |
rs569269898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69874442 | ACTTGCGAGATTTAT[A/T]TAGCAGCCTTTTTTG | 11060 |
rs569287412 | in-del | -/T | 1.6494e-05 | 0.00287171 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931273 | GTTGGGGTTATTGAG[-/T]TATTTCAGTGTGAGT | 11060 |
rs569312084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868364 | CCACATGCCCTTTCT[C/G]GGAAGGGAGGGCAGG | 11060 |
rs569327912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69867102 | CAGCCTCCTGAAGTG[C/T]TGGGATTATAGGCAT | 11060 |
rs569327923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859660 | CTGACCATCAGCGGG[A/G]GTCCCTCTCAACTCC | 11060 |
rs569352343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932873 | GCAGAGAGAGAGAGC[A/G]CTGTGGCCCGCAGCG | 11060 |
rs569368346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770433 | GCTGCACACGTGGAG[G/T]TTCTTGGAGGATGGC | 11060 |
rs569371506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926505 | CCTGGAAACATGCAG[C/G]TTTGGAGCTGGATCT | 11060 |
rs569413700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919528 | ACTAACTGCCTAAAC[A/G]GTCTCCTATACCGTG | 11060 |
rs569431940 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898873 | CACTCCCAGATACTT[A/T]TTCTGTATTTAGTAG | 11060 |
rs569448164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875121 | GGTTTGTTTCCAGAC[A/T]ATCACAATAAAGTGA | 11060 |
rs569458242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826469 | CCCAGCTACTTGGGA[A/G]GCTGAGACAGGAGAA | 11060 |
rs569539809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69818942 | CAAAGACAGTATTTA[C/T]GTCTAATTAACATCC | 11060 |
rs569563931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769671 | TTGAAGAGCTCTTAC[C/T]GTGTGTCCTCTGCTT | 11060 |
rs569594079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860086 | CAGACCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 11060 |
rs569619449 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880427 | TTTTTTTCCTCCATG[A/G]TATTCTTTGATCGTT | 11060 |
rs569624078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823117 | GCCTGCGCAACAGAG[C/T]GAGACTGTGTCTCAA | 11060 |
rs569648391 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761327 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 11060 |
rs569668267 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873226 | TGAGTGGAAGAAATT[G/T]ATTTGGGTTCCTTTG | 11060 |
rs569668674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935755 | TCAGGGAAGGAAGGC[A/G]GGTAGCGGTAGCAGA | 11060 |
rs569680795 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876138 | AATTTTTGTATTTTC[A/T]GTAGAGATGGGGTTT | 11060 |
rs569693197 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848746 | TTTAAGAATGCATGT[G/T]AACGCACATGAGAGA | 11060 |
rs569704665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69817929 | CCTTTATGCTCCTCT[C/T]TTTTTTTCCCTACAG | 11060 |
rs569706178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69831643 | TTATTAACTTGAAGC[C/T]ACTTGCAAATCTGAG | 11060 |
rs569722691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69872638 | AATGTAGGACTAAGT[A/G]TTGTTGCTAAGAGCT | 11060 |
rs569730009 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936360 | GTACTTCATCCAGGA[C/T]ATGGAGATACTGGGC | 11060 |
rs569737674 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829085 | TAGAATCCCAGGAGC[C/T]GTCTTCGATACCCGA | 11060 |
rs569750017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69783156 | CTGGGATTACAGGTG[C/T]GTGCCACCATGCCCG | 11060 |
rs569778765 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846368 | ACGTAGAAAGTTGAA[A/C]AATGCAAAGCCAAAC | 11060 |
rs569789825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804527 | CCTGCTTAGGGACTT[A/T]CCATTGAATCCATCG | 11060 |
rs569799317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893299 | CACACCAAGGTGGCC[A/G]GGAGCCTGGCACAGA | 11060 |
rs569804020 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941454 | TTAGCTTGCCACAGC[A/C/G]CAGCCTCTTCTGTCC | 11060 |
rs569838873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69846547 | CCAACATGGCGAAAC[A/T]TCTTCTCTACTAAAA | 11060 |
rs569847898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69768780 | TCCACGGGGCTTCCA[A/G]TAGTGTACCTCCCTG | 11060 |
rs569878142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69797649 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTAGGCA | 11060 |
rs569899920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839342 | AGTGTGGACTAAACA[C/G]TTAACTAGACAGAAG | 11060 |
rs569938297 | in-del | -/AC | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69816747 | CACACGTATACATAT[-/AC]ACACGTATACATATA | 11060 |
rs569977436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852753 | ATATATGTTTTGCCA[A/G]TATTTTCTCCCAGTC | 11060 |
rs569987138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69811941 | ATGTGTCTGGTTCCT[A/G]AAGGAGAAGGATACT | 11060 |
rs570001666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903577 | ATCGAGACCATCCTG[A/G]CCAACATGGTGAAAC | 11060 |
rs570009063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897485 | TGAAGCTTCCATGAA[C/T]TCTCTGATCTCATTC | 11060 |
rs570052216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890871 | CAGAGGCTGAAACAC[A/G]TTTCTGAGGTAGAGC | 11060 |
rs570053408 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69937857 | ATGTGACAGGAGGTC[A/G]TCAGTGGTCAGCCTT | 11060 |
rs570057109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931483 | TTGAGGCTCGATTTA[A/G]AGTTCTTTTCTTTTT | 11060 |
rs570071475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69786847 | CAGGTTCATTAAGTC[A/G]TTATAAGACAAACTA | 11060 |
rs570074400 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791813 | GTGTGAGCCACCGTG[A/C]CTGGCCCCCACCTCG | 11060 |
rs570114604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69891200 | TTTCTGCCAGCGATC[A/C]TTCCAGTTCATAGGC | 11060 |
rs570133405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69830843 | AGCCTTCTCTCTAGA[C/G]CTGGGGTGGACTCCA | 11060 |
rs570148247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904038 | GCATTAGGAGCAGAT[A/G]TTATAAAAGAGAGGC | 11060 |
rs570155215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69787948 | CCTAGGTCCCAGCCT[A/G]GTCCAGGCCACCATT | 11060 |
rs570184752 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915900 | AAAAATTAGTTGAAT[A/G]TGATGGTGCATTCCT | 11060 |
rs570186249 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833600 | AAAGTAGCATTAGAA[A/G]GTATTGGTAACCAGT | 11060 |
rs570202719 | in-del | -/C | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760496 | CCATGCCCGGCGAAT[-/C]TTTTTTTTTTTTTTT | 11060 |
rs570227430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69885767 | TTAAGTGTTAAGTGG[A/G]GATATCAATTGTAAC | 11060 |
rs570230388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931100 | TGACAAAGACAAATT[A/G]TTCATTTTCTGAGAA | 11060 |
rs570231004 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | WWP2 | GRCh38.p7 | 16:69793859 | AACCTTGTGGCTGTT[G/T]ATTAGTTTTACAAAG | 11060 |
rs570237948 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924852 | GTGCCCTCAGTCTGG[G/T]TGGACGCTGCACACC | 11060 |
rs570254419 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894979 | CATGCTTTTTCTCCC[A/G]CAGCCATTGGCTGCC | 11060 |
rs570268510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69782293 | ATCTCAAACAAACAA[A/G]CAGACAAACAGAGGG | 11060 |
rs570270125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916519 | GGGAGGTTAATTCTG[A/G]GGTAGGAGCAGTAGT | 11060 |
rs570292032 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769965 | CTGCAGCCTCTAAGC[A/G]ATTCCCGTGCCTCAG | 11060 |
rs570292105 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923837 | TTGCCGAATGTTTTT[A/C]ATGTGTTAACTACAA | 11060 |
rs570305953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789938 | TTGACTGAAAGCCTT[A/G]CCAATAACAGAAACA | 11060 |
rs570311744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69815618 | TGGTGAAACCCCCGT[C/G]TCTACTAAAAATACA | 11060 |
rs570329435 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908532 | TGATCTATAGTGGAT[C/T]CTGGTCCATTGATTC | 11060 |
rs570338796 | in-del | -/AGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808180 | AATTTCATATTAGTG[-/AGA]ACATGCAGTATGTTT | 11060 |
rs570357875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69921887 | AAGACCATCCTGGCC[A/T]ACATGGTGAAACCCT | 11060 |
rs570378386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69768298 | TGATTTAAATCATTA[A/C]TACTAATAATAACTA | 11060 |
rs570380665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69877268 | CACTTGGACTTTTAC[A/G]CTGTGTTTGAGGGAT | 11060 |
rs570391590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876675 | AGCCATAAAATGTAT[G/T]TCTTAAATAGTAAGA | 11060 |
rs570412100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69828547 | AATTTTGTATTTTTC[A/G]TAGAGACGGGTTTCT | 11060 |
rs570448445 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836953 | TTTGAGACGCAGTCT[C/T]ATTTTGGTTGCTTAG | 11060 |
rs570482354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770690 | GTCGCAAGTCAGGGG[C/G]AGTCTTGGGGAACTA | 11060 |
rs570507458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929048 | GGTCCCAGGACCAGG[A/G]ATCAGCTGTGAGGGA | 11060 |
rs570513424 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821326 | TATCAGCTGAGAGCT[A/G]TTGGAAAGAAAAGGT | 11060 |
rs570518889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771306 | CAGGCTGGAGTGCAG[C/T]GTGCTATCTTGGCTC | 11060 |
rs570528150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843254 | GTTAAGACCTCCTAC[A/G]CTTAGAGTCCAAATA | 11060 |
rs570530718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69862109 | TCGCTCTTGTTGCCC[C/T]GGCTGGAGTGCAATG | 11060 |
rs570530806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869434 | CTCTTTTGCCACGCT[C/G]TCAGGCTGAAGTGAT | 11060 |
rs570543597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800657 | GCAACCTCCGCCTCC[A/C]AGGTTCAAGCGATCC | 11060 |
rs570596003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69781508 | TGTGCCATCACACTC[A/G]GCTAATTTTTGTATT | 11060 |
rs570607692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69836093 | CAGACGTGAGCCACC[A/G]TGCCTGTGCATAAAA | 11060 |
rs570615556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863613 | GCCACTTCACTCCAG[C/T]CTGGGTGAAAGAGTG | 11060 |
rs570622139 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787406 | CCAGCCTGGGAAACA[C/T]AGGGAAGCCCTGTCT | 11060 |
rs570634765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774459 | ACGAGGTTTTGCCCT[A/G]TTGTTCAGGCTGGTC | 11060 |
rs570638246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69781029 | CTAGACCCTGTCTCA[A/G]AAAAACAGGTTGGTC | 11060 |
rs570666858 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69821873 | ATTTTTCTTTGTTTT[G/T]TTTTTTTTTTAAATA | 11060 |
rs570668085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765151 | GCAGTGAGTTGTGAT[C/T]GTGCCACTCATTGCA | 11060 |
rs570676317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864513 | TACTTTGCATCCTAA[C/T]CCAGACTTATTACTG | 11060 |
rs570727354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69778883 | TGCCCTCAAGTGATC[C/T]GCATGCCTGAGCCTC | 11060 |
rs570736018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69830011 | CTAAGCTGGAATGCA[A/G]TGGCGCGATGTTGGG | 11060 |
rs570748718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69889436 | TGGAGATTATAAGCA[C/T]GGACCTGTGAATCAG | 11060 |
rs570772160 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901338 | TACTTCCAGTGTATT[C/T]TTCTTAAGTTTAATT | 11060 |
rs570805131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763437 | AGCAAAAGGAGTTTC[A/T]TGAGTGCAGTGTAAC | 11060 |
rs570814068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907195 | ACTCCAGATGTTGAC[A/G]GTGTAGCCTATTAAT | 11060 |
rs570845761 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69875964 | ATTTTTTATTTTTTT[A/T]TTTTTTTGAGATGGA | 11060 |
rs570856877 | snp | C/T | 0.15698 | 0.23205 | intron-variant | WWP2 | GRCh38.p7 | 16:69820533 | ACAGGCGTGAGCCAC[C/T]GCTCTTGGCCCCCTG | 11060 |
rs570861993 | in-del | -/AC | 0.0123036 | 0.0774623 | intron-variant | WWP2 | GRCh38.p7 | 16:69832765 | GCCAGGCTGGCTTGA[-/AC]TCCTGAACTCAAGTG | 11060 |
rs570868015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827455 | GTATACGCTTTATAA[G/T]CACTAATCCAAATCT | 11060 |
rs570902589 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69813199 | TGGAGTTTTGCTCTT[C/G]TTGCCTAGGCTGGAG | 11060 |
rs570912726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847229 | AGCTGGGACTACAGG[C/T]ACATGCCACCATGCC | 11060 |
rs570924355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920331 | GTGCGCTCTGCACAC[C/T]TTCTTGGGCTAGGCT | 11060 |
rs570924509 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904332 | TTTTAAATCAGAAGG[A/G]CATTCAGAGGGAGAA | 11060 |
rs570928809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939178 | GCGGACAGCTCAGAG[A/G]GAGGGGGAAACCTAG | 11060 |
rs570968293 | in-del | -/CCA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780177 | TAAACGTTTGTGTGT[-/CCA]CAACAACAACGTATA | 11060 |
rs570985617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913313 | GGTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 11060 |
rs570999906 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921389 | CTCCTCTTGCTGGGC[G/T]TCAACTGAGACCTTG | 11060 |
rs571009963 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940315 | CCTCCTGGACTAGTT[C/T]GGCGAGGAGACTGGC | 11060 |
rs571011501 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896741 | TATTTTTTTTTTTTT[-/TTT]AAACACTAACTACAG | 11060 |
rs571017239 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69906376 | GCACCCGGCCTTACG[-/T]TATCTGTTTCTGGAC | 11060 |
rs571023869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880683 | ACGAAATCTTTGTCC[A/C]GTTTTGGTTGCTGTC | 11060 |
rs571024547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69783279 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 11060 |
rs571075847 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69901735 | AGCTGATAATGCTCT[C/T]ACCAAGACTGAAATT | 11060 |
rs571096869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69842358 | TTTTAGATTCAGGGG[G/T]TACATGTACAGGTTT | 11060 |
rs571096937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856330 | TGCAAAGGGGCACAA[G/T]GAAATTTTGGGAGCA | 11060 |
rs571105629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69855671 | ATGTAACCATGAGGA[G/T]ATCTGGGGAAAGAGA | 11060 |
rs571140670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900804 | GCTGGAATTACAGGC[A/G]TGAGTCACCGTGCCT | 11060 |
rs571150223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69939784 | AGGCAGGCATGGTGG[A/G]GCTATCAGAGCCCTG | 11060 |
rs571170757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932931 | GTGGGCATGTCTTCC[C/T]GCTTGGTGTTGGGTT | 11060 |
rs571171873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847794 | TAATTTATTCATGAG[C/G]GATCCACCCCCATGA | 11060 |
rs571186315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806292 | TGCTCAAGATAGACT[A/G]TTCCTTGAAAATTTT | 11060 |
rs571192809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887432 | ACACAATTTTGCTGT[C/T]AGGCAAATTTTTTGC | 11060 |
rs571213008 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790413 | TCATAAAGGTCTTCA[A/T]CCTCATCATTTTCAT | 11060 |
rs571261032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790109 | AAAATTAGCCAGGCG[G/T]GGTGGCAGGCGCATG | 11060 |
rs571274003 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764232 | TGAGACAGGATCTTA[C/T]TCTGTTGCCCAGGCT | 11060 |
rs571278980 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761694 | AATGCGATTGGATTA[C/G]TGTGGAGGGGCTTTT | 11060 |
rs571286595 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69762617 | GCGCGGGGGTTGCTC[C/G]GAAATGGGTGCCCCG | 11060 |
rs571296767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69860830 | AACATAGCAAGACTC[G/T]ATCTCTAGTTAAAAA | 11060 |
rs571324346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812672 | TGGCAGATTCCCCTC[A/C]ACTTGGGGCTGTCTG | 11060 |
rs571347469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790679 | CTCCTGGGTTCAAGC[A/G]ATTCTCATGCCTCAG | 11060 |
rs571359389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69853643 | ACTCAGGGACTGACG[A/G]AGAGGACTGTTGCAG | 11060 |
rs571402745 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762092 | ATGGGGCTAGTACCT[A/G]TCCCTGCCTCTATAA | 11060 |
rs571404387 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778459 | ACTTGAGTACGTGTA[C/T]GGAGTCATCTGTTCG | 11060 |
rs571409049 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910667 | GCCTGCCTTTGCCTC[C/T]CAAAGTGCTGGGATT | 11060 |
rs571422019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792443 | ATCTCACATAAAGTC[A/G]TGACTCTGTGTATAA | 11060 |
rs571445418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875346 | CTGGTGGAAGGTCTC[G/T]CCTCGATGTTGATGG | 11060 |
rs571448619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925103 | GCCTGCTTCCCGGGC[C/T]TTCCTACCATGCCAG | 11060 |
rs571459764 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888435 | TTAAAAAGAATCTCA[A/G]TCGCCTGGGGCAGAA | 11060 |
rs571465972 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69785293 | GGGAGGAAGGGGAGC[A/G]GATATGAGTTTTTAA | 11060 |
rs571471141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69919800 | GACTTTTTTTTTTTT[C/T]TTTTTTTTGAGACAA | 11060 |
rs571486031 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | WWP2 | GRCh38.p7 | 16:69818208 | TTTATTTATTTAATT[A/T]ATTTATTTTATTTTT | 11060 |
rs571538017 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69832021 | TTTAATAGAGGCAGG[A/G/T]TTTCACCATGTTGCC | 11060 |
rs571555019 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69849148 | GAAAAATAAACTCAG[C/G]CGGGTGTGAGTCCAC | 11060 |
rs571566950 | snp | A/T | 0.0015225 | 0.0275487 | intron-variant | WWP2 | GRCh38.p7 | 16:69888009 | TCTCATTCTTAGTTG[A/T]TCTTTAAAGTATGAT | 11060 |
rs571568681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69871303 | AAGTGAATGACAACA[A/G]CAAAAAGTGTCAACA | 11060 |
rs571581172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917998 | ACAGCGTCTGGCAAC[A/G]TCAGTGCTCTGCCCC | 11060 |
rs571582597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791822 | ACCGTGCCTGGCCCC[C/T]ACCTCGGCCTCTTAA | 11060 |
rs571595892 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69885238 | AAAAAAGTCATAGTG[-/T]TTTTTTTTAAAATTG | 11060 |
rs571598027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783330 | CTTTCATTCTTAGAG[A/T]AATATGGTGAATTAA | 11060 |
rs571641951 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933383 | GTGTTGGGGTCTGGG[C/G]GTGAAGGGAGGGCAA | 11060 |
rs571652248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885941 | TATGTTTAGTTCCTG[A/C]TATGATTAGCTAGAA | 11060 |
rs571726110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69825511 | TTTGTGGAGTAGGTG[C/T]CATAGTTTACCTTTC | 11060 |
rs571746735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69905981 | GTTAGCCTGTAGCTC[A/G]TGGTAGATTCTCAGT | 11060 |
rs571751303 | snp | G/T | 3.30879e-05 | 0.00406729 | missense | WWP2 | GRCh38.p7 | 16:69937568 | GCTGTGCGGCATGCA[G/T]GAGATAGACATGAGC | 11060 |
rs571758387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932234 | CTGGGGAGGCTGAGG[C/T]GGGAGAATCGCTTGA | 11060 |
rs571762733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69860210 | ATTCTTTAAAGGAGT[C/T]GGGGAGGTGATGAGT | 11060 |
rs571817990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814350 | GTATATTAAACACTA[C/T]GAATTTGTACTGAAG | 11060 |
rs571818732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846486 | GCATTTTGGGGAGGT[C/T]GAGGCGGATGGATCA | 11060 |
rs571857380 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816743 | CATGCACACGTATAC[A/G]TATACACACGTATAC | 11060 |
rs571882951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910728 | GTGGCTTCTTCTTAA[C/T]CTCTCTTGTCTAGGA | 11060 |
rs571926144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809117 | CTGCTGTTGCTGGCA[C/G]CAGCCGTAGCACGTT | 11060 |
rs571926895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923216 | ACAATTACTTTTGCA[C/T]CAACCTAATAAATGT | 11060 |
rs571937438 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69796221 | TGTCTAGAGCTTACT[C/G]TCAGAGTTTCAGGAA | 11060 |
rs571958214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69864784 | TGGAGTGCAATGGCT[C/T]GATTTTTAATAGAGA | 11060 |
rs571963353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873494 | GTGGGGAGTCCCAGG[G/T]CTGCCGTCTCAGCTG | 11060 |
rs571971784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896961 | ATAATCTTCCAGTAT[A/C]TGCTTTTAAAATCCA | 11060 |
rs572019627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69858071 | TGGGAGATTAGGGCC[C/T]GGTTGGTTTTGTTCC | 11060 |
rs572023150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890975 | CACTTGAACATGTAC[A/G]ATGGTCCAGAGAAGG | 11060 |
rs572037081 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941223 | TAGGTCATATTGAAA[A/T]CTTCAAGGTGACCAT | 11060 |
rs572047317 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69816305 | AATAATTACTTAGCC[C/T]AGTGCAGTGGCTCAC | 11060 |
rs572067341 | in-del | -/AAAAAAAAGGG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826947 | CCACCTCAAAAAAAA[-/AAAAAAAAGGG]GGGGGGGCGGAGAGA | 11060 |
rs572085071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815885 | TTATTTTCTTTCTGA[A/G]TAGCTAAGACTACAG | 11060 |
rs572086422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69850112 | GAAAAGTCGGCCGGG[C/T]GCAGTGGCTCACGCC | 11060 |
rs572099220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69930810 | CCAGGAATTCGAGGC[C/T]GCAGTGAGCCATGAT | 11060 |
rs572100716 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941700 | CCCGCCCCTTGCCTC[A/G]ATATTGCCAGTTTCT | 11060 |
rs572122757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822050 | TTTTGTATTTTTTGT[A/G]GAGACAGGGTCTCCC | 11060 |
rs572125667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884238 | AGTTATCTTAGAATG[C/T]TCCCATAGTATTTGA | 11060 |
rs572126380 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916339 | AGCTGGGACCAAGGG[C/T]GCACACTCCACCACC | 11060 |
rs572170895 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837950 | ATGAAGGCTAGGGCG[C/T]GGTGGCTCACTCCTG | 11060 |
rs572176870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788902 | GCAGCCATCACAGAT[A/G]GGAGAGTGGCTCTCA | 11060 |
rs572183665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849044 | TTAAAAGATCTGTAA[A/T]CTCGGAGACTTATAA | 11060 |
rs572221495 | snp | A/G | 0.00130149 | 0.0254765 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931255 | ACTGGGGCTCCCGTG[A/G]CAGTTGGGGTTATTG | 11060 |
rs572229827 | in-del | -/CA | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941347 | CGGGTGCCTTCCAAG[-/CA]CAGTCTCCATGCTCC | 11060 |
rs572244243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936060 | AGCAGGTACTGATGG[C/T]CTTTATTTTGTCTGC | 11060 |
rs572270570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845125 | CACAAAACCTCTCGG[A/T]TCCCCAGTTTTTTTC | 11060 |
rs572304868 | in-del | -/AATG | 0.00318978 | 0.0398085 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761137 | ATAAATAAATAAATA[-/AATG]AATAAATAAATAAAG | 11060 |
rs572305557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934877 | GAGCCCAGAGAGGGC[A/G]CGCCAGTCCATGGGC | 11060 |
rs572308294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802329 | GTACATTCACCTTGT[A/G]CAACCATCACCACCA | 11060 |
rs572335985 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766007 | TGCTAACAGCTTCCA[C/T]ATGTGTGTCTAGCCT | 11060 |
rs572349978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69843337 | CATTTTATACCTGTG[C/T]TAGTGGTGCAAACTC | 11060 |
rs572388374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883191 | GCAATTCTGTAAGGC[A/G]TGATGGACTTGTAAC | 11060 |
rs572415096 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918734 | CCATCTGGCCTGTTC[C/T]CCTCAGAGCAGTCTT | 11060 |
rs572462065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793414 | GCATTAGAGAAAGAG[A/T]TTAATTGACACAAAA | 11060 |
rs572463991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800113 | AAGAGTCTTTCTTTT[C/G]TCTCCAAGCCTGTCC | 11060 |
rs572475600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69763239 | TTTCTTCCGTTTAAA[C/T]TATTCAGTTTCCCTT | 11060 |
rs572479894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856619 | ATCTCACTAAAAATA[C/G]AAAAATTAGCTGGGT | 11060 |
rs572491119 | in-del | -/G | 0.000286763 | 0.0119708 | intron-variant | WWP2 | GRCh38.p7 | 16:69936037 | AGGAGGGACGTCTCT[-/G]GGTGGGAAGCAGGTA | 11060 |
rs572507580 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | WWP2 | GRCh38.p7 | 16:69780269 | CCTTTTTTTTTTTTT[C/T]CCCCTCTTGGCATTA | 11060 |
rs572508051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69808085 | AGAAGTTTCCCATTG[G/T]CCCTTCTAGTTAATT | 11060 |
rs572512936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69920455 | CTCCTTTTGAGCTGG[A/G]CCCAAAAGATTTTGC | 11060 |
rs572532904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894812 | TAGATAAACTCCAAG[G/T]GTGTCCCTTACAGTC | 11060 |
rs572553401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788180 | CCAGCCTGAGCAACA[C/G]AGCAAGACCCCCGTC | 11060 |
rs572594283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69895476 | TGTCAGATCGGTACA[A/G]AAGTTCCTAAAGTGG | 11060 |
rs572608396 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909939 | CGGCCCTCTGACTGT[G/T]TTTGTAAATAAGGTT | 11060 |
rs572614587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829473 | TCATTCCAGTCCAGC[C/T]CCGTTCATCTCTGCC | 11060 |
rs572665842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69787226 | TTGTCATCTTGTAGC[G/T]GTAATTCTTGAAGAA | 11060 |
rs572687980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69915258 | TGTACTTATAGTATT[C/T]TACATTGTCATCCAA | 11060 |
rs572693810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821407 | GTTCCAACAATCCTG[C/T]ACCCTGTGTCACTGA | 11060 |
rs572702763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69883763 | TTAAACAGAAGAGCT[A/G]CTATGGGTGAACCAG | 11060 |
rs572719175 | snp | C/T | 0.000287911 | 0.0119947 | intron-variant | WWP2 | GRCh38.p7 | 16:69938984 | GGGCAAAGTACTGGG[C/T]CCCGTGGGTTGCCTG | 11060 |
rs572723364 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837051 | ACCTCTGCCTCCTCA[G/T]TATCTGGGACTACAG | 11060 |
rs572745737 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69914517 | AATCCCAGCACTTTG[C/G]GGGGCCAAGGCAGGA | 11060 |
rs572754647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827853 | AACTGATAATTTATT[A/C]TAAAGACTTAACCTT | 11060 |
rs572806504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69912526 | CAAGAGATTAAATGC[A/G]GATGCTATCTCCATT | 11060 |
rs572825078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69868947 | GGCTGGAGTGCAGTG[A/G]TACAATCTCGGCTCA | 11060 |
rs572835690 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69925754 | TGTCCCTGAGCAGCT[-/G]GGGGGGCTATTGGCT | 11060 |
rs572840623 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69820784 | TGTGAATTTTGTTCA[C/G]TTTTGTGTACCTACA | 11060 |
rs572844364 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69875573 | CTGCAGCTTTATCAA[C/G]TAAGTATATGGAATA | 11060 |
rs572849208 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780829 | GGCAAGATGGTGAGA[C/T]CCTATCTCTACAAAA | 11060 |
rs572866213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69792678 | TGGTAAGAGGTACAC[A/G]ACATAACTTATGTAG | 11060 |
rs572882158 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69833830 | GCAGCCCCTGCCTGT[G/T]ACTTGCCCAAAGCTT | 11060 |
rs572904085 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69769784 | ATTTAGAGAGGGTAG[C/G]TATGATTTTGTGAAA | 11060 |
rs572932297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69814075 | AAGCCCTTGGGATTC[A/G]GGGACACACTTGTTT | 11060 |
rs572941543 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927564 | CCTTGGGAGGCCTCC[A/C]CACAGCAGCAGTGCC | 11060 |
rs572963045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69763704 | TCTTTCTTGTTTGCT[A/G]GCCTCTTCCTGCTAG | 11060 |
rs572985862 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795679 | TTTTTTTTTTTTGTG[A/G]GAGTCTCTCTCCATC | 11060 |
rs572987503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776975 | TGTTGTAGACCAGTA[A/G]TCTCAAGCTTTTTTG | 11060 |
rs573036114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906141 | GCAGTGGTGCGATCT[C/T]AGCTCACTGCAAGCT | 11060 |
rs573045249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869251 | AAAAGAGAGTCCACA[C/T]TGAGTATTTCCACAG | 11060 |
rs573072125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69901902 | GTTACAGTGAGTTGA[G/T]ATTGCACCACTGCAC | 11060 |
rs573080873 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806859 | CAACTTCTTGGATTT[G/T]TCAGATACCATATTT | 11060 |
rs573081585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861978 | CAAATACCGCTTACC[C/T]GGATTGGAATGTGAG | 11060 |
rs573091103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798516 | TTCATATTTTTTTTG[G/T]TGTGTGTACTCACAT | 11060 |
rs573092033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907367 | ATGCTCACATCGTCC[A/G]CTTCTATATCAATAG | 11060 |
rs573111339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69763074 | AAACAAAAAAAGAAA[A/G]TAAATTAAAAAAATA | 11060 |
rs573129281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798929 | CCCTGTGGCACCTCC[A/G]ACTTTTTCTACCTAT | 11060 |
rs573136878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819082 | TTCATTTTCTGTCCC[A/G]TCAGCACCTCCTGTC | 11060 |
rs573143438 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69808337 | TCAAGTGATCCTCCC[A/G]CTTTGGTCTCCAAAA | 11060 |
rs573161281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779113 | CGCCACCACACCCGG[A/C]TAATTTGTTATATTT | 11060 |
rs573163790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805005 | ACTGAGTCCTTTAGT[A/G]TAGGTTTGCAGTAGT | 11060 |
rs573195490 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855458 | TGTGCCTTGGTTTCT[A/G]TAATAATGCAGAATC | 11060 |
rs573199482 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761685 | GATTAAGGGAATGCG[A/C]TTGGATTAGTGTGGA | 11060 |
rs573248292 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829271 | GTCCTTCCTTTCCTC[C/G]GGCTTGTTTTCCACA | 11060 |
rs573261660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69852043 | GGTAAATACAAAGGA[A/G]CATGATTGCTGGGTC | 11060 |
rs573262603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69910926 | GGCTCACCTGTACGC[A/C]CTGCATAGCTTACTA | 11060 |
rs573278096 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852136 | CCAGTTTGCATTGCC[A/G]CCAGCAGTGAGTGAG | 11060 |
rs573278941 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69867522 | CAGGGTGTAGCTGAG[G/T]ATGGAGGCCAGGGCT | 11060 |
rs573286163 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877501 | AGGCTGTTTTACTTT[C/T]TTATCACTCAAGTGT | 11060 |
rs573314637 | snp | A/G | 6.61135e-05 | 0.00574912 | intron-variant | WWP2 | GRCh38.p7 | 16:69939302 | GCTTTGGGAAGGGAC[A/G]TCTCTGCTGACGTCG | 11060 |
rs573340744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69894203 | GCCTCGGCCTCCCGA[A/G]TAGCTGGGACTACAG | 11060 |
rs573344298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933022 | GATGTTCCTTTTTTC[C/T]GTGGTGACCTCCTCT | 11060 |
rs573364717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69887597 | TTTTAGCAGAGACGG[C/G]GTTTTGCCATGTTGG | 11060 |
rs573400938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859735 | GCCCCCTCCACCTTC[A/G]AGCCAGGAAAGGAGT | 11060 |
rs573449210 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762231 | AAGGCCTCCTCGAGG[C/T]CAGAGGTGCCCAGGC | 11060 |
rs573468240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69880579 | ACACAGTATGGCTTC[A/G]TCCATTTTTAAGTTT | 11060 |
rs573475508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69938784 | TGGGAAGAGAATACC[C/T]AGCCTGAGGTGTCCC | 11060 |
rs573481981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792591 | AATGTGTCAGTGGAG[A/T]GACCTGGCCAACTCC | 11060 |
rs573501599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893725 | TTTTTGTATTTTTTA[A/G]TAGAGCCAGGGTTTC | 11060 |
rs573528955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69873780 | TAGCAGCTTTGTTCT[A/G]CCAGATGCCTGTGTT | 11060 |
rs573537335 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795168 | TTCAGCCAGGTAGGT[C/T]GAGGCTGCAGTGAGC | 11060 |
rs573540603 | snp | G/T | 0.000399281 | 0.0141238 | missense | WWP2 | GRCh38.p7 | 16:69937190 | GGATGGCTTCAACGA[G/T]GTGGCCCCGCTGGAG | 11060 |
rs573575628 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845065 | TCAGGAGATGCAGAT[A/C]GAATCCTGGCCTGTC | 11060 |
rs573604741 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69846040 | GGGTGACAGAGCCAG[A/T]CTCCATCTCAAAAAA | 11060 |
rs573613751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69804021 | AGTGTTTATTGCCCT[A/G]TTAATGTCCTTTGCT | 11060 |
rs573628798 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873939 | TATTTTTAGGTACCA[A/T]TACTTGTTGTCCTTA | 11060 |
rs573648635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936630 | TGGGGGAACCAAAGC[C/T]GAGGTCCTTAGTTAC | 11060 |
rs573668580 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869273 | TTTCCACAGTTCAGT[C/T]GTACTCTGTCTCCAT | 11060 |
rs573681090 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760533 | GTTTTAGTAGAGATG[G/T]GGTTTCACCAGGTTG | 11060 |
rs573689046 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69804397 | TAGGGATCTAATTCA[-/T]TTTTTTTCCCTAATA | 11060 |
rs573699084 | snp | C/T | 6.64662e-05 | 0.00576443 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931783 | AGTGGCAGGCTGGCC[C/T]GATGCTCTGTCTTCC | 11060 |
rs573705658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791026 | GAGTCTTTTGCCTTG[C/T]TTCTGCCCTTTTGAG | 11060 |
rs573708489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923927 | CAACACACAGACACA[C/G]GCCCCCATGACTTGG | 11060 |
rs573744157 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936289 | CGGTAGACATCTCCC[A/C]ACTTGGTCTCCTGTG | 11060 |
rs573759284 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69880809 | AGCTGATCTTCAGTA[G/T]AAAGAACTTCTGTTG | 11060 |
rs573760145 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823247 | AAAGAAAAGTACTAA[C/T]GAGATATTTTACATA | 11060 |
rs573779964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803174 | TTTTTGGCTGAATTA[C/T]TTTTATTTTCTTATT | 11060 |
rs573783319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69930740 | AGCTCGGTGTGGTAG[C/T]ACACTCCTGTAGTCC | 11060 |
rs573785725 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837391 | TTTTGAAGACAAAAT[A/G]TGTCTCAAGGTGTTG | 11060 |
rs573803483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784044 | GTCTCCCAGACTCTT[C/T]TAGGGTTTTGCAAGG | 11060 |
rs573841778 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802277 | TGTAAAATTAATCAC[A/G]TTAATAATTTTTAGG | 11060 |
rs573846731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923110 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 11060 |
rs573858112 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69886670 | GAGACTGAGGCATGA[G/T]AATTGCTTAAACCTG | 11060 |
rs573868872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839939 | CCCTCCAGCCTGATA[A/C]AACAGTGATTTCATT | 11060 |
rs573874588 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819247 | TCCTATGGAACGGTT[C/T]TGAATGCAGCAGCCA | 11060 |
rs573901758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917618 | CTGTGACAGGGCCTG[C/G]CCGGCTGTGCTAGGC | 11060 |
rs573922760 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP2 | GRCh38.p7 | 16:69854841 | CAAGTGTGGGCCACC[A/G]CGCCTAGCCTCTTTT | 11060 |
rs573958583 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WWP2 | GRCh38.p7 | 16:69915877 | CCATGTCTACAAAAA[A/T]TTTTTTAAAAAATTA | 11060 |
rs573966779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932279 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC | 11060 |
rs574007824 | in-del | -/TGGA | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69808915 | CTTTGGTTCATAGGG[-/TGGA]TGGATGTATGCTTAC | 11060 |
rs574028820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69925972 | CCACCTTTTTATTTC[C/T]GACATAGCTGTGAAA | 11060 |
rs574035936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69890935 | CGTGATGAGGGCCAC[A/G]TGTGGGCCTGGGGAG | 11060 |
rs574058763 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784033 | GACATTGGGAGGTCT[A/C/T]CCAGACTCTTTTAGG | 11060 |
rs574066925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69878084 | AAGTGTTGGGATTAC[A/G]GGTGTGAGCCACCGT | 11060 |
rs574103222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69795430 | TTATTTGCACTAGCC[A/G]TATTTCAAGTGTCAA | 11060 |
rs574107433 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837876 | AAGATTCTGTGGTCA[C/T]AGCCCAAAAAAGTCT | 11060 |
rs574116165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766331 | CAACAGCCTCCTAAC[G/T]TGTCTCCCTCTTCCA | 11060 |
rs574119900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782009 | TTTTCGGAGCCGGGC[G/T]AGGTGGCTCATGCCT | 11060 |
rs574121740 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785812 | GTTGTTTTTTAGTAT[A/G]GATGGGGTTTCATCA | 11060 |
rs574150326 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812366 | GATGGGGTTTCATCA[C/T]GTTGGCCAGGCTGGT | 11060 |
rs574151305 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69865887 | AGAAAGGAATGCCGG[G/T]CAGTTGCTGTGTGGA | 11060 |
rs574179962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767338 | TGAAGTGACCCTCAC[A/G]AGGTCAGATAGCTAA | 11060 |
rs574185486 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942177 | TGACCTCAGGGTCAC[A/G]TAAGGGCTTGCCACC | 11060 |
rs574201694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69884149 | TATTCCTTGAAAAAA[C/T]ACACACATGTGTATG | 11060 |
rs574245329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69916577 | CATAGGAATGGAAAA[C/T]GGAAAGTCAGTGGCA | 11060 |
rs574260374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865261 | TGCCATGTTGCCCAG[G/T]CTGGTCTCGAACTCC | 11060 |
rs574284191 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69872278 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 11060 |
rs574295936 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69816478 | TAAATATATATACTT[A/T]ATATATGTAATATAT | 11060 |
rs574328055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69802179 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 11060 |
rs574330774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815030 | TTTGAGATGGAGTCT[C/T]ACTCCTCTGTCATTC | 11060 |
rs574345305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69870259 | TCAGTGAATATTATA[C/T]ACTTCTGTAGCCATT | 11060 |
rs574349176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903101 | AAGCCAGTTGAGGGG[G/T]TTCATAGAAGGACAT | 11060 |
rs574351667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69764401 | TTTTGCTATGTTGCC[C/T]GGGCTGTTTTCAAAC | 11060 |
rs574364433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782412 | CAAGAAGGCTCAGGT[C/G]GGGCAGGAGGAGGAT | 11060 |
rs574393805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69809057 | GTTATTTAAGTGGAT[A/G]TTTTCCAGTGGTTAT | 11060 |
rs574404792 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69863156 | TCCACATTCTTGCTG[-/T]TTTTTTTGACCATAC | 11060 |
rs574410667 | in-del | -/GAACAAGTCAATATTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899952 | ATATTGTAAATACCT[-/GAACAAGTCAATATTT]ATCTACAATGTTATT | 11060 |
rs574411478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69863663 | AACAAAGAAACAAAC[A/G]AACAAAAGATACAGA | 11060 |
rs574437838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69829485 | AGCCCCGTTCATCTC[C/T]GCCCACTTTCCTGAA | 11060 |
rs574443486 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895936 | ATGGTTAGTTTGTGA[C/T]TCTGCAGGGATTGTT | 11060 |
rs574448010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69856027 | CTATAGTCCCAGCCA[C/T]TGGGGAGGCTGAGCT | 11060 |
rs574455467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869875 | GACTGCCTCAACACA[C/T]TGGACCAAAGACTCC | 11060 |
rs574506385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69935407 | TACTCACCATTGGCC[A/G]CCAGCTCTCGCTGTC | 11060 |
rs574506406 | snp | C/T | 4.95307e-05 | 0.00497623 | intron-variant | WWP2 | GRCh38.p7 | 16:69939319 | CTCTGCTGACGTCGG[C/T]GTGTTTTACCTTGGA | 11060 |
rs574508302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915133 | CAGGCCACCTGTCCC[A/G]TCTGAGAATCTGGGG | 11060 |
rs574521889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69856886 | CTTGGCATATTTTTT[C/T]CCCTATTCATTTCAT | 11060 |
rs574524656 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902314 | TTGGGACGTAGGGTT[C/G]GAACATGGTTCATAT | 11060 |
rs574567578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896908 | TGCCTGGCACCACAT[A/G]TACAGATACACGTAT | 11060 |
rs574568020 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69844217 | AATAGTTGGGTCTCA[A/C]GGGGTGATGAATGAC | 11060 |
rs574620805 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921811 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11060 |
rs574641145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69815719 | TTGAACCTGAGAGGC[A/G]GAGGTTGCAGTGAGC | 11060 |
rs574641439 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941180 | GCCAGCCTCCAACAC[A/G]GGGACTCTGCCGTAA | 11060 |
rs574646311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850099 | GTGATTAAAAGATGA[A/G]AAGTCGGCCGGGCGC | 11060 |
rs574664138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69765413 | AGCAGTACAAGAAAG[C/G]TAAGGATCCCCACCC | 11060 |
rs574676678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883016 | AAATTAGCCAGGCGT[G/T]GTGGCACTCGCTTGT | 11060 |
rs574704181 | snp | A/G | 1.70023e-05 | 0.00291563 | missense | WWP2 | GRCh38.p7 | 16:69939873 | TTCCACCCTACAAGA[A/G]CTACGAACAGCTGAG | 11060 |
rs574727946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883859 | AGATTTGCAGCTGCA[A/T]AAACAGTCAGATCCG | 11060 |
rs574729479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779302 | GGTTTTACAATTCCA[A/G]ATGCCTACATTATAT | 11060 |
rs574735430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876748 | GGATGTTGTGTTAGC[A/G]GGCATGAAAACAACA | 11060 |
rs574736093 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870300 | TTATTTATTTATCCT[-/T]TTTTTTTTTTTTTTT | 11060 |
rs574738801 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918099 | CCTCTGTGTTTAAGG[A/G]ATCAACGTGTCTAAA | 11060 |
rs574750046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69888850 | GCTGGGGCTACAGGT[A/G]CACACCACCACACTG | 11060 |
rs574763691 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823475 | TCTCTTTTTCTTGTG[-/T]TTTTTTTTTTTTGAG | 11060 |
rs574777359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69799544 | TTATCCTTCCTTAGG[A/G]ACTGGAAACTTTCTG | 11060 |
rs574823070 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938849 | TCTCATGCACACACA[A/G]CCTCTTAGCAAAAGC | 11060 |
rs574844134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69901175 | AAATCTTATGGTTCT[C/T]CCCGGAAGTGGCCAA | 11060 |
rs574907425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763589 | AAAAATTAGTTTTTG[C/T]AGCAGCGCCTATGAG | 11060 |
rs574908202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934193 | CTTCCCTCTCCTGGT[A/G]AAGTGTGCCAGGGGC | 11060 |
rs574909004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927278 | ACAGGAAGAACAGCC[A/G]GACCAAGTGAGAGTG | 11060 |
rs574911239 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69833734 | GAGCCTCTTGCCAGC[G/T]GAATATTTTCATTAT | 11060 |
rs574917465 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888323 | CGGGGGTGGAAACAA[C/T]GTGGTTATTTATTAC | 11060 |
rs574917595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861979 | AAATACCGCTTACCC[A/G]GATTGGAATGTGAGA | 11060 |
rs574922887 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69851084 | GCTCAATCTCAGCTT[-/A]ACTGCAACCTCTGCC | 11060 |
rs574935913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794002 | AGCTTACTGCACTTT[C/T]TGCCTCCTGGGTTCA | 11060 |
rs574937174 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827126 | ACTCCTGCATACATG[C/T]CTAATGTTTAACTGA | 11060 |
rs574945229 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69921576 | GTTTCCCTTTCCCAA[A/C/T]TCCTAGTGTGCTAAT | 11060 |
rs574953044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907328 | CACAGACAAAATCAC[A/G]CATAAGCAAATAGAA | 11060 |
rs574960292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876370 | TTTTTTTTTTTTTTC[A/G]TTTTTTGTTTTTGAG | 11060 |
rs574980482 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852610 | ATATGCTTATATTCC[A/G]TCTGTATATCTTCTT | 11060 |
rs574985685 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762261 | CCAGGCCTAGGTGGC[C/T]CGCACCTGCGAGCCT | 11060 |
rs574997427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69814018 | GCCAGTGGCACAAGC[A/G]TCTCCAGGAAATATG | 11060 |
rs574997458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69806742 | GTCTGTAATATTTTT[A/T]ACTTTAAATTTTTGC | 11060 |
rs575025897 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP2 | GRCh38.p7 | 16:69841651 | TCTCTGGGTGTATTA[C/T]GGAGAAATGCCCCCG | 11060 |
rs575090070 | in-del | -/TTAT | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69809043 | TCTTCAAACCCAGAG[-/TTAT]TTAAGTGGATGTTTT | 11060 |
rs575102167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69828036 | TGGGTGACTGTAATG[A/G]GTAACTGGTGCTGAA | 11060 |
rs575122291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69843285 | TTATACTTGTTATAC[A/G]TATTACAAATGACGT | 11060 |
rs575126263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920705 | GGTGGGAGGATCACT[G/T]GAGCCCAGGAGTTTG | 11060 |
rs575153386 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69834251 | ACTCCAGCTGCCCTG[C/G]CCTCCCTGCCATTCC | 11060 |
rs575174188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69934728 | CCTGGGCCCCCTCTT[A/G]ACAAGTCCTATGCAA | 11060 |
rs575190245 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863779 | GTATTCTTTCTCTAA[C/G]TTTGACCTCTTCTTG | 11060 |
rs575230332 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP2 | GRCh38.p7 | 16:69847329 | ACTTCAGGCGATCCA[C/T]GCACCTTGGCCTCCC | 11060 |
rs575239374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910800 | AAGTAAAGATATTCA[A/G]TGGTACCTTCTAAGG | 11060 |
rs575239902 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69835618 | TCTATATGTTATTAT[A/T]GTATATGGCTGGGTG | 11060 |
rs575258327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929113 | CGGCTTCCATGCTGC[A/T]CACAGCTGGGAGCAA | 11060 |
rs575267688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69798416 | AAAATCTGGAAGGCA[A/G]TTTACCAACGATAAA | 11060 |
rs575313979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69783393 | GATAAGTCAGGCACC[A/G]GGCTTGGTGGTCCGA | 11060 |
rs575321033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69791225 | TACTTCTTTTCTTTT[C/T]TTCTTTCTTTTTTTT | 11060 |
rs575337323 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907311 | GTTCATCTAGTGTTT[C/T]TCACAGACAAAATCA | 11060 |
rs575351261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69784954 | AAGAAAAGAAAGAGT[C/G]GTCGAGTGCAGTGGT | 11060 |
rs575354150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69770824 | ATGTGGGGCTCCCAC[A/G]CATCTGGTGTCAGAA | 11060 |
rs575359291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881868 | AGCTATTTTTTTCTA[C/T]TTTTAGTAGAGACAG | 11060 |
rs575360742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69770062 | AGATGGGATTTCGCC[A/G]TGTTGGCCAGGCTGG | 11060 |
rs575406116 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815065 | TGGGGTGTAGTGGGA[C/T]GATCTTGGCTCACTG | 11060 |
rs575412323 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780977 | AGGTTGTAGTGAGCT[A/G]TGATCATGTCACTGC | 11060 |
rs575427604 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69919918 | CCACCTCAGCCCCCT[C/G]AAGTAGCTGGGACTA | 11060 |
rs575457544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938696 | AATTCTGGAACATTT[C/T]ATCTCCCCAAAAACC | 11060 |
rs575460600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875428 | TTTCTAATAAGACAA[C/T]ATGAAGTTCACAGCA | 11060 |
rs575466932 | in-del | -/A | 0.496105 | 0.0439572 | intron-variant | WWP2 | GRCh38.p7 | 16:69850386 | CTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 11060 |
rs575470088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69805524 | TTTTGCTTTCTTCTT[C/T]TTTTTTTATTTTATT | 11060 |
rs575474403 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782814 | CATTGTCACTTAGCC[A/G]TAGCTACATTTATTT | 11060 |
rs575477731 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69778493 | TGCTGAGACAGAGTG[A/T]GAAGTCTGGGCCTCA | 11060 |
rs575495604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69826781 | CTCTAATAAAAATAC[A/G]AAAAAAAATTAGCCG | 11060 |
rs575499365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69906109 | ACGGAGTCTTGCTCT[C/G]TCGCCCAGACTGGAG | 11060 |
rs575506808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811735 | ATCCAGTCTGGATGA[C/T]AGAGCCAGACCCAGT | 11060 |
rs575523125 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837649 | GTCCTCCAGGAAGGA[-/G]GAAAAAAAAGTGCCA | 11060 |
rs575523287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69873558 | TGCTGGAACATCCGG[C/T]GGTAGCTGAGCCTGG | 11060 |
rs575536115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69819334 | TCCCTATGAGCCCAC[C/T]GGCCCCCTGTGATGC | 11060 |
rs575547427 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69832121 | GGTGTGAGCCACTGC[A/G]CCCTGCCTTCTTTGT | 11060 |
rs575555543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69776921 | GCTTATTAGGTTCTG[C/T]AGTGTTTGTTTAATC | 11060 |
rs575586732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69859050 | TGGAAATTGAATTGT[C/T]ATTTATTTGCATTCA | 11060 |
rs575587649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777524 | GAGGCTGGTCTCGAA[C/T]TCCTGACCTCAAGCA | 11060 |
rs575587996 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69785531 | TGATATTCCAAAATC[A/T]CATACAAGTAAAAGA | 11060 |
rs575599742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69768558 | GAGGTTGCAGTGAGC[C/T]GAGATTGCATCACTG | 11060 |
rs575679758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69866924 | CTCACTGAAACCTCC[A/G]CCTCCTGGATTCGAG | 11060 |
rs575698110 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858453 | CATGTTGCTGGTTTA[C/T]GTTCCCTGGCGCCTT | 11060 |
rs575701582 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905272 | TAGCACTCTGGTCCT[C/T]AACCAAGAGTTGTCC | 11060 |
rs575701827 | in-del | -/T | 0.0755793 | 0.179102 | intron-variant | WWP2 | GRCh38.p7 | 16:69897095 | AGGTCTCTCCCCGTC[-/T]TTTTTTTTTTGTTTG | 11060 |
rs575703473 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69872782 | GACAGTGCCGTCCAC[C/G]TGCGCATGGAACTTC | 11060 |
rs575722443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69865852 | GGCCAGAACCACACC[A/G]TAGTCAGTGGCCTCT | 11060 |
rs575724694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69766250 | ACATCCAACTCAGCT[C/T]GTCCACAAAGCCTAC | 11060 |
rs575734216 | in-del | -/ATTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884976 | TTTCTGAACTTTCTT[-/ATTA]ATTGACACTTGCCTA | 11060 |
rs575738364 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821868 | CGGCTATTTTTCTTT[C/G]TTTTGTTTTTTTTTT | 11060 |
rs575740608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69859878 | CCCCCCACCCCCGCC[C/T]CGCCCGATGATCCCC | 11060 |
rs575741549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69900275 | TTTGCTCCCATTGAT[C/T]GTTCTTGATAGTAAC | 11060 |
rs575742463 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69867387 | AGCTCCTTGAGGTCA[C/G]GGACTCTGTTTTATC | 11060 |
rs575780366 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794528 | GGGAGACCCGGTCTC[-/A]AAAAAAAAAAAGAAA | 11060 |
rs575790917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69789525 | GAGCCACCGTGCCCA[A/G]CCTCCTATAGTTCAA | 11060 |
rs575817227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885977 | AGTAGATGATATCTC[A/G]AAGAGGGCAGCCAGA | 11060 |
rs575823979 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808599 | CAGAGACAGGGTTTC[G/T]CCATGTTGGCCAGGC | 11060 |
rs575830815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69797861 | GCATTACACTCCAGC[C/G]TGGGCAACAAGAGCC | 11060 |
rs575838890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69769090 | TTGGGAGGCCAAGGC[A/G]GGTGGATCATGAGGT | 11060 |
rs575844338 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855867 | TGCTTTATGTATTTC[A/G]AGGTTATTTCATTGG | 11060 |
rs575859696 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808896 | CGTATGTACAGATCT[A/G]GGAGCTTTGGTTCAT | 11060 |
rs575878961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790143 | TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGGGA | 11060 |
rs575912318 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780146 | GTGGTTCCTTCCCGT[C/T]GTACTTTTATACTTT | 11060 |
rs575919250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69767204 | CCAGTTTAGGCCTCC[A/G]GGATGGATGGATAAT | 11060 |
rs575922171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69899599 | GCCAGGTGTATTGGT[A/G]CATGCCTGTAATCTC | 11060 |
rs575953771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69891939 | GGGCCTCCAGACTGT[A/G]CTGTCTCAGCTTCCC | 11060 |
rs575953778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69885246 | TCATAGTGTTTTTTT[A/T]AAAATTGAGTAAAAT | 11060 |
rs575954926 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942038 | GTGGGGTGCAGAACA[A/G]TAACAGCTACAGACT | 11060 |
rs575979937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69897705 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 11060 |
rs576001580 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761032 | AAGGAGAATTGCTTG[A/T]ACCTGGGAGGCAGAG | 11060 |
rs576021019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69803099 | TTGTAAAAAAAAAAA[G/T]CCTTTTTTTTTCCTA | 11060 |
rs576022664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69903793 | AAAAGAAAGAAAGAA[A/C]AATGTGTTTAAGTTT | 11060 |
rs576037794 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761500 | ATTGCATGAACCGGC[A/G]AGACGGAGGTTGCAG | 11060 |
rs576068772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69936118 | CCTCTATAAGAGCTT[A/G]TGGAGAGGAATGTCC | 11060 |
rs576108508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69843427 | GGAGAGGGTTGGCAC[A/C]TTTGTTTATTGTTTA | 11060 |
rs576114916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69904460 | TGCAGCCTCCAACTC[C/T]TGGGCTCAAGTGATC | 11060 |
rs576118675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69935374 | CCAGCAGGACAGACC[A/G]GTAAAACCCTAGACT | 11060 |
rs576132072 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941191 | ACACGGGGACTCTGC[C/T]GTAACTGGAATCTTC | 11060 |
rs576132269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69936543 | CCACCTGTGGCCCAT[C/T]GGTCACTGTGGATGC | 11060 |
rs576143001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879148 | TCCGAGATTTAGAAG[C/T]TTATTTTAGAGGTTT | 11060 |
rs576161988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69836531 | AGGTCTCAAATAGAA[C/G]AGAGGAGGGTTATGT | 11060 |
rs576170538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69844188 | TGTTTTCCGTGTCTC[A/G]GTAGGTGACTTACAA | 11060 |
rs576201275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69864015 | ACAAGCAAAGCCTCT[A/G]TGAGCTTTTGCATAC | 11060 |
rs576216839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69816833 | TATATGTGTAAACTC[A/G]TTTATTCTTCCTCCG | 11060 |
rs576220720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69913500 | GAGCAAGACCCTGTC[C/T]CAAAAAATTATAATA | 11060 |
rs576227984 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795491 | GGCAGCACAGATGTG[C/G]AACATTTTCGTCATC | 11060 |
rs576236595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879842 | TATAAGTTTTCCCAT[A/G]TCACTGTTTTGCATT | 11060 |
rs576241457 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848155 | TCTTAGTTAAGAAGC[C/T]GTCAGCTGGGCGCAG | 11060 |
rs576257588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931685 | GCAGACTTTCCAGGG[C/T]GTGAGTCTTGGTGAC | 11060 |
rs576288733 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837778 | GTGTCCTGGAGCCAG[A/G]AGGCTGGGCGCCTTT | 11060 |
rs576301494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69845981 | CCTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 11060 |
rs576308031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69929698 | ACACTGTTGGCCTGA[C/T]GAGAGCTTAAAAGGG | 11060 |
rs576324180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69831358 | CTAGAAAGTTCTTTC[A/G]TACATTTGCTGTGAA | 11060 |
rs576324233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839795 | GCAACTAATTTCTTC[A/G]TCTGTACGCCATCAA | 11060 |
rs576393337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931311 | ACAGCAGCAGGTATC[A/G]GAATGTTTGTGTCTT | 11060 |
rs576398359 | snp | A/G | 6.59207e-05 | 0.00574073 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925435 | TTGTGTTTAGTCTTC[A/G]AGTGCTTCGACTGAC | 11060 |
rs576406903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69877553 | TTTCCTTCAAGAACT[C/T]CTCCTTTGCATTCGC | 11060 |
rs576416702 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69820860 | CACACACACACACGA[A/C]GTTGAAAGAGTGACT | 11060 |
rs576431180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69914303 | TAGCCCAGAGGATAA[A/C]AAAAGACTCACCCCA | 11060 |
rs576433995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69896291 | GCTCAGCTAATTTTT[G/T]TACTTTTTGTAGAGA | 11060 |
rs576436941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838934 | TCTTTGACTTGATCC[A/T]GAATTTTCTGCTAAG | 11060 |
rs576460605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69850056 | TATTCACTTGATATA[C/T]ATGAATGCCAGGCTC | 11060 |
rs576461786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69794868 | AGGAGATAGTAGCCA[C/T]AGGCAATTTGTATAT | 11060 |
rs576463650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69787458 | GCCAGGCATAGTGGT[G/T]CATGCTAGCTGGTCC | 11060 |
rs576490046 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789043 | CATGGAGTTTAAAAA[A/T]CTTAGTTTTTAATTT | 11060 |
rs576503399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69801136 | GGAGGTTCCAGTGAG[C/T]CGAGATTGCGCCACT | 11060 |
rs576503435 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69883284 | TGTCCCTGGTTGACC[A/C/G]GGGTGACCGTGGGCC | 11060 |
rs576551333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788192 | ACAGAGCAAGACCCC[C/T]GTCTCTAAAAAAAAA | 11060 |
rs576551477 | snp | C/T | | | utr-variant-5-prime, splice-donor-variant | WWP2 | GRCh38.p7 | 16:69762389 | CTTCTGTGGCCACGG[C/T]AGGTAGCGAGCGCTG | 11060 |
rs576562648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69822506 | TCTGGGAATGCATCA[C/T]GGGAGACTTTGCCTG | 11060 |
rs576585036 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69774859 | CCTGTAACCCTAGCT[A/C]CTCAGGAGGCTGAGG | 11060 |
rs576592287 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940563 | TGAAGGTTTGTCTAA[A/G]CTGCCTGGGTATCCA | 11060 |
rs576619925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69829572 | TGGTCTTCCTCCCTG[C/T]CCTGCCCTACCCTGC | 11060 |
rs576641657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69781230 | CACAGCATGATGAGG[A/G]TGGGGGGATACTGGG | 11060 |
rs576650190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923043 | TATAGGTGCCTGCCA[C/T]TATGCCTGGCTAATT | 11060 |
rs576651720 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911622 | GGGCCTCCAGTCACT[G/T]TTCTGTGCAAGATTT | 11060 |
rs576654631 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940929 | AATCCCTTTGCTAGA[G/T]AGGGTCCCCCAGGCA | 11060 |
rs576669742 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922605 | TGACATCTCTCATTT[G/T]AGGGGAATGTGGTAG | 11060 |
rs576678398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69781967 | CACCTCTTCAAGGCC[C/T]CACCTCTCAATACTG | 11060 |
rs576704451 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914188 | TTAGCAAGAACTTGC[A/G]GAATAGCAGGAAAGA | 11060 |
rs576715080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909066 | GGAAACAAAAGGCGC[A/G]TGGGAGGCCAAGATT | 11060 |
rs576720838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779244 | GCGTGAGCCACTGTG[C/T]GTGGCCCCGGCCGGT | 11060 |
rs576733500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869332 | TCCAGAGTTTGCTAC[A/G]TTTCTCCCTTTTTCT | 11060 |
rs576756281 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778454 | AAATTACTTGAGTAC[A/G]TGTACGGAGTCATCT | 11060 |
rs576764306 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765200 | GTGAGACCCTGTCTC[-/A]AAAAAAAAGAAAAAG | 11060 |
rs576774738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907463 | AAAAGGTCAACTTCT[C/T]CTAGACAGTACCCAA | 11060 |
rs576789940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69915317 | TCCATATTGAGAGGA[C/T]GAGGGGAGGAGATAG | 11060 |
rs576791997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69788724 | TTAATTTATTTCATT[A/T]GTTGACTGTCTCCTT | 11060 |
rs576809229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69771877 | GGGTCAATATGGTGC[C/T]TTATCCCTATTGTCA | 11060 |
rs576815836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69779943 | AGAGATGAAGATAAC[A/G]AACAGTCATAAAAAC | 11060 |
rs576816534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69893763 | TGGCCAGGCTGTGCT[C/T]GAACGCCTGACCTCA | 11060 |
rs576823547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69835395 | GGTTCCTCTGGCTCA[A/G]TTTTTTTAAAAAGCA | 11060 |
rs576830178 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69828070 | TGTGTGCATATGTAC[-/T]TTTTTTTTTAAGTAA | 11060 |
rs576833555 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776363 | CTTGACTCTTTACCA[A/G]GATAATCTTGTAAAG | 11060 |
rs576851242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69915739 | GTTTCAAAACTATAT[A/G]CATATGACTTCGGGC | 11060 |
rs576852367 | snp | A/C/G | 1.64738e-05 | 0.00286995 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69908779 | GGAACAGCGAGAGCT[A/C/G]CCCAACGGACGTGTC | 11060 |
rs576867380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69876336 | TGTATTTGGTTTTTT[G/T]GGGGCATGTTTTTTG | 11060 |
rs576873063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869287 | TCGTACTCTGTCTCC[A/G]TTGCCATGCAGTGTT | 11060 |
rs576909056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69769821 | TTTAGTCTTCCTCCC[A/G]TTTCCTGGCCTATAA | 11060 |
rs576912549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69827945 | GAGATTTACCAAGAC[A/G]GATGAAATCTTTGTA | 11060 |
rs576941005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69869758 | ATCCAAAGATAATGA[C/T]GGTTAAGATTTTGGT | 11060 |
rs576942963 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP2 | GRCh38.p7 | 16:69862352 | TTACAGGCGTGAGCT[A/G]CCGCGCCTGGCCCTT | 11060 |
rs576950922 | in-del | -/TTTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864119 | CTGTAATCCCAGCAC[-/TTTG]TTTGGGAGGCCAAGG | 11060 |
rs576958411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69808172 | TAGTATTGAATTTCA[C/T]ATTAGTGAGAACATG | 11060 |
rs576980376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69792776 | AGCTCACTACAGCCT[C/T]GACCTCCTGGGCTCC | 11060 |
rs576983604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69849539 | TAAGACATAGTCCCT[G/T]CTCAAAGTCCCTGCT | 11060 |
rs576985566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69857365 | CCCAAAGTGCTGGGA[G/T]TACAGGTGTGAGCCA | 11060 |
rs576985885 | in-del | -/TTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806933 | TTTGCCCTAGATCTG[-/TTTT]TTTTATTTATTTATT | 11060 |
rs576995650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69800330 | CCAAACCCTAGCCAG[A/C]CTTTTGTAATTTGAT | 11060 |
rs577036086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69920186 | GATTGCTCATTGTAC[A/C]GGGAGGAAACCATGG | 11060 |
rs577036478 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783949 | GACAGAGTGAGATAC[C/T]ATCTCTAAAAAACAT | 11060 |
rs577042915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69821323 | TGGTATCAGCTGAGA[A/G]CTGTTGGAAAGAAAA | 11060 |
rs577054187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69793208 | ATACAAAAAAATTAG[C/T]TGGGTGTGATGGCAG | 11060 |
rs577059447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69856199 | CTAAGCTTAAGAAGC[C/T]AGACATAGAAGCTTA | 11060 |
rs577073006 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | WWP2 | GRCh38.p7 | 16:69894274 | TGGTAGAGATGAGGG[G/T]CTCACTCTGTTGCCC | 11060 |
rs577083290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69764300 | GACCTGCCTGGGCTC[G/T]GGTGATCCTCCCATG | 11060 |
rs577110870 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904883 | TGTCATGTTAAATAA[A/G]TAAGCAAGAGGCCGT | 11060 |
rs577117826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861699 | GAAGAATTGAGGGGG[G/T]TGCAGGTGGGAGTAG | 11060 |
rs577122062 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874479 | CACTGCAGTTATGCA[A/T]GAAAAAGAAATTTGA | 11060 |
rs577122788 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899795 | GGCATAATTTAATTG[A/G]CAGTGTTTTTTTTCT | 11060 |
rs577122826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP2 | GRCh38.p7 | 16:69853950 | ATTGGTACTGCCTGG[C/T]TCTGGGGCAGAGTCA | 11060 |
rs577142803 | snp | A/C/G | 0.000115339 | 0.00759329 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888169 | TGCCCCAGCCACACC[A/C/G]GCTGAAGGAGAGGAA | 11060 |
rs577174592 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | WWP2 | GRCh38.p7 | 16:69904939 | CAGTTCTTACATAGC[-/A]AACTACAACCTAACT | 11060 |
rs577184327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69854768 | GTTGGTCATGCTGGT[C/G]TCGAACTCCTGACCT | 11060 |
rs577193500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69763806 | ACTTGATAAATATTT[A/G]GTGAATAAATGCATT | 11060 |
rs577199201 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798600 | TTAAAGCAATAACTA[A/T]AAAGAGCCGGAACAT | 11060 |
rs577233118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906376 | CGCACCCGGCCTTAC[A/G]TATCTGTTTCTGGAC | 11060 |
rs577239674 | snp | A/G | 4.86488e-05 | 0.00493174 | intron-variant | WWP2 | GRCh38.p7 | 16:69842157 | ACAAAGAGCTAAGAA[A/G]TTGCTTAGAGCTATT | 11060 |
rs577241872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69840654 | TGGGAAGGGTACGCT[A/G]TGTTCTTCTAGAGAT | 11060 |
rs577260939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69861206 | TCAGGGTACCTCAAG[A/C]CATCAATGGCCACGT | 11060 |
rs577275392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69938969 | GAGAGCTCCACGTTC[A/G]GGCAAAGTACTGGGC | 11060 |
rs577294450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69906757 | TCGTGGCATGCACTT[A/G]TTTTCCTAGCTACTT | 11060 |
rs577295803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846310 | ACATAATGTTGAACA[A/G]GAGAAGCAGGTCATA | 11060 |
rs577306360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69813439 | AGTGCTGGGATTACA[G/T]GCGTGAGCCACTGCG | 11060 |
rs577309785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69938053 | GGGTTTTGTTGTTGT[A/C]GTTATGAAATACAGC | 11060 |
rs577319559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69927628 | CAGATCCCCCTGGCC[C/T]TGTGGTTAGCCTTGG | 11060 |
rs577326776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69847558 | GGATTACAGGCATGC[A/G]CCACCATGCCTGACT | 11060 |
rs577352883 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839991 | TTTTTCCATGCCACG[A/T]GGCAAAATGTGAAGA | 11060 |
rs577358182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69846658 | CCCCCGAGGTGGAGG[G/T]TGCAGTGAGCCGAGA | 11060 |
rs577383617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69928297 | GAAGCAGATTTGAAG[A/G]CTCAGGAACTTCCTG | 11060 |
rs577389073 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69834605 | AATCTCGGCTCACTG[A/C]AACTTCTGTTTTCCG | 11060 |
rs577415926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69875674 | ACTGCTTTCTTTGCT[C/T]ATCCATAAGACACAA | 11060 |
rs577422921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69812995 | ACTCTGATGCCTATA[G/T]ATTTTTATTTTTGAA | 11060 |
rs577487626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69798978 | TTTTAGGTGTTCCTA[A/C]ACCATTGAGCTCATA | 11060 |
rs577523064 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863878 | ATTCACCTCTGTTGC[C/T]GCATGTACCAGCACT | 11060 |
rs577523988 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890375 | GGCAGCTCTGGGATG[-/T]TTTTTTGTGAGGTTT | 11060 |
rs577541345 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP2 | GRCh38.p7 | 16:69886757 | GGAGCGAGACTGTGT[C/T]TCAAAACAAAACAAC | 11060 |
rs577584465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69926084 | GTAGATTTCTCCTCG[C/T]GCTTGGTAGCCGCCT | 11060 |
rs577591356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69848112 | TTGATTCATAAAATT[C/T]TTCATTAATAGGGAT | 11060 |
rs577601434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69823264 | AGATATTTTACATAC[C/T]TTTTGGCCTCAGGTG | 11060 |
rs577617980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69917482 | GGTTGGGAACAGAGT[C/G]AGCTTCCCCAGAACC | 11060 |
rs577656898 | snp | C/T | 1.65381e-05 | 0.00287555 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931829 | AAACCCTATGACCTG[C/T]GCCGCCGGCTCTACA | 11060 |
rs577703548 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913961 | CCTATAATCCCAGCT[A/C]CTCGCGAGGCTGAGG | 11060 |
rs577705545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69790362 | AAATCATAAGGAGGA[A/T]AAAAATTTTACTATT | 11060 |
rs577720970 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP2 | GRCh38.p7 | 16:69784889 | ACACTTCAAGGAAAA[C/T]AACACAGTATTTGTT | 11060 |
rs577723670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69777035 | ATATCTTAAAACAGT[A/G]TATGTGTGTGTGTGT | 11060 |
rs577762983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892117 | CACCTAGCCTGGCAC[A/G]TAGTGGGACTCCAGG | 11060 |
rs577779229 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789292 | TGGAGTGCAGTGGTG[C/T]GATCTCGACTCACTG | 11060 |
rs577807055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69777470 | CACGACCAGATAATT[G/T]TTGTGTTTTTAGTAG | 11060 |
rs577809039 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850018 | TAGGAGGAAGGAAGG[C/T]AAATCTCTGCCGTTG | 11060 |
rs577826756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69892928 | GGGGATAAATTCCCA[A/T]ATCCTTAATAAGGCC | 11060 |
rs577828519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69832984 | CTAGCCTCCCATGAA[C/G]GTGGGACCGCAGGTG | 11060 |
rs577837575 | in-del | -/ATTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866850 | TTTATTTATTTATTT[-/ATTT]TTGAGACGGAGTCTC | 11060 |
rs577844582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69907105 | CTTGTGGAAGCAGGT[A/G]TCAGAAGTTGGAGCT | 11060 |
rs577862437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69881093 | CCTTGTGAAATACCC[A/G]AGGTTATAGAAAGCA | 11060 |
rs577889754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817087 | AATACTTTGTAATAT[A/G]GCCACTGTTTTGGGG | 11060 |
rs577894059 | snp | C/T | 0.000317018 | 0.012586 | synonymous-codon, missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931885 | GGACTATGGGGGCAT[C/T]GCCAGGTGAGCTTGA | 11060 |
rs577914839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69911744 | TTTATTTCTATTCTT[C/T]CTGAAAACCCACTAA | 11060 |
rs577926650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69817560 | CAGCCAGATGCTTTG[G/T]TTTTGTTTTGTATAA | 11060 |
rs577928242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69782533 | GTCATGTAAGAGGAG[A/T]TGGAGAATTGCTATG | 11060 |
rs577934952 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69882411 | CTTTCTTTTGCTAGA[C/T]TATTGGGCTTATTGA | 11060 |
rs577960302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909670 | TGACTTGAAGTCAAA[G/T]GAAGTTACCAAAGTT | 11060 |
rs578004983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69775547 | TTACATTGCCCATCT[A/G]TTCTCATGTGTTGTC | 11060 |
rs578029747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69919093 | AAGTGACCTGCCCTC[C/T]TCGGCCTCCCAAAGT | 11060 |
rs578049812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69782057 | GGAGGCTGAGACGGG[C/T]GGATCACCTGAGGTC | 11060 |
rs578050533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69879053 | AAAAAGTTTAACCTC[A/G]TTGCGTTTTCTCATT | 11060 |
rs578089272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69872739 | GGGTGTGCAGGGGCC[A/G]TCCCGATGGGGGCCC | 11060 |
rs578100690 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785259 | GACAAAAGACAAGGT[A/C]GTAGAGATGATGGAA | 11060 |
rs578168484 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP2 | GRCh38.p7 | 16:69860543 | AATTTGGCCACCTGG[A/G]TGGAAAGTCCAGGAA | 11060 |
rs578175539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69776202 | AGATGAAACAGAAAG[C/G]CTAAAGAGGGCTGGA | 11060 |
rs578185366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP2 | GRCh38.p7 | 16:69907420 | CAAAGCAAGCATTAC[C/T]GCAGAACTGACTGTA | 11060 |
rs578193257 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932149 | AGCCTGACCAACATG[A/G]AGAAACCCCGTCTCT | 11060 |
rs578194172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69811050 | ATGAGCCACCATGCC[C/T]GGCTGGAATTTTCAA | 11060 |
rs578194898 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP2 | GRCh38.p7 | 16:69768450 | CCCGTCTCTACTAAA[A/C]ATACAAAAAATTAGC | 11060 |
rs578217506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP2 | GRCh38.p7 | 16:69898619 | CTTTGGTTTCTTCTT[C/T]TATAAATTGCCTATT | 11060 |
rs578225377 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760662 | AATTTAATTTGTATG[C/T]ATGATAGAATCCATC | 11060 |
rs578261130 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930483 | ACCGTGTCTCCACAA[A/C]AATAAAAAAGATTAA | 11060 |
rs745320438 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818710 | AGGGTGCCACAATCT[A/G]TGGGTTTTCTGTCCA | 11060 |
rs745323302 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906623 | AGGGTAGGCACGTTG[A/G]TTTGTGATACCAGCA | 11060 |
rs745337347 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831150 | CAGAGACTCTTAATC[C/T]TGGCGTCCTTGGCCT | 11060 |
rs745393492 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791584 | TGGAATGTAGTGGCA[C/T]GATTACAGCTCACTG | 11060 |
rs745402432 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904504 | CTCCTGAGTAGGTAC[A/G]ATTACAGGTATGTGC | 11060 |
rs745415079 | snp | A/C/G | 0.000268571 | 0.0115852 | intron-variant | WWP2 | GRCh38.p7 | 16:69917695 | TATATTCATTCTGAG[A/C/G]TTCCTATTTCCAGCT | 11060 |
rs745424513 | snp | A/G | 1.76649e-05 | 0.00297189 | intron-variant | WWP2 | GRCh38.p7 | 16:69935817 | GGCAGTGCCCAGGGA[A/G]GGCCAAACCTCTGTG | 11060 |
rs745449729 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849693 | GTATGCCTGAGTCCC[A/G]GCTCTTTGGGAGGCT | 11060 |
rs745454433 | snp | C/T | 9.89462e-05 | 0.00703302 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908872 | CATCAACTGAGAAGA[C/T]CTGAGACTCTGGAAC | 11060 |
rs745479631 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766006 | ATGCTAACAGCTTCC[A/G]TATGTGTGTCTAGCC | 11060 |
rs745497802 | snp | A/G | 3.18051e-05 | 0.00398767 | missense | WWP2 | GRCh38.p7 | 16:69939052 | AGATGGACAACGAGA[A/G]GAGGATCCGGCTGCT | 11060 |
rs745498839 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807525 | TCGGGAGGCTGAGTC[A/G]GGAGGATTGCTTGAG | 11060 |
rs745507601 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | WWP2 | GRCh38.p7 | 16:69934124 | ATAGGCAGATTCATC[A/G]CCATGGTAAGGGGGC | 11060 |
rs745516118 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891967 | CCCATACTGATCCTG[C/G]TTTGCATTTATCACA | 11060 |
rs745533742 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774281 | TTTTTTTTTGAGACA[C/G]GGTCTTGCTCTGTCA | 11060 |
rs745540670 | snp | A/G | 1.65002e-05 | 0.00287225 | intron-variant | WWP2 | GRCh38.p7 | 16:69840266 | GCCCTGACAGATGGT[A/G]AGTGCCGCCCTGCTC | 11060 |
rs745544263 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845601 | CCTTTCCTCTCCTTC[-/T]TTCCTCTGCTTGGTA | 11060 |
rs745580617 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929468 | AGACAGGACAATGGA[C/T]GGGTGTATTACGTGA | 11060 |
rs745593689 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849542 | ACATAGTCCCTGCTC[-/A]AAAGTCCCTGCTTGT | 11060 |
rs745604227 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902617 | TGACCAAGATGCAGT[A/G]TTGAGACCCGTGGGT | 11060 |
rs745614713 | snp | A/G | 3.44098e-05 | 0.00414774 | intron-variant | WWP2 | GRCh38.p7 | 16:69937680 | CCCAGGCCTTGGCAG[A/G]GACATTTGGGCCATC | 11060 |
rs745655782 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937372 | ATGGGTTTGATTTGG[A/G]ACCCACCCTTCCCCA | 11060 |
rs745682729 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928422 | AATCCCTCTCAAGGT[C/T]CAGAATCACCAGCTA | 11060 |
rs745690603 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777092 | AAACAGTATATGGAT[-/AT]ATATATACACATATG | 11060 |
rs745693805 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894572 | AAATTAACTAGCGTG[A/T]AAGAAGCCAACTGGA | 11060 |
rs745696975 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796886 | AAGATAGTTACTGCT[A/G]TAAAAAATCTGAAGG | 11060 |
rs745714616 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763330 | TGTGTTATGTTCCTT[A/C]GAACTGTGACCTGGA | 11060 |
rs745716057 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827529 | AAAAAAACTCCAATG[C/T]ATACAAGGGAATTTT | 11060 |
rs745717247 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901333 | TTGAGTACTTCCAGT[A/G]TATTCTTCTTAAGTT | 11060 |
rs745723425 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931790 | GGCTGGCCCGATGCT[C/T]TGTCTTCCCAGATCA | 11060 |
rs745755357 | in-del | -/TTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806938 | CCTAGATCTGTTTTA[-/TTTA]TTTATTTATTTATTT | 11060 |
rs745772985 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937003 | TGGGTCTGGGTGTGC[A/G]AAGTGGGCTCTGCTG | 11060 |
rs745788396 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931603 | CATGGTGCCCGAAAC[C/T]AGTGGCAGGCCGACG | 11060 |
rs745806723 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876735 | TGGGCTACAGCATGG[A/G]TGTTGTGTTAGCGGG | 11060 |
rs745820112 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857545 | CATTGACTGGCTCCC[A/G]GCCTGAAGGTTTTCT | 11060 |
rs745845066 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | WWP2 | GRCh38.p7 | 16:69888062 | GAACCCACAACAGCC[A/G]CTGATCCCGAAGAAC | 11060 |
rs745856288 | in-del | -/AGAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809787 | GAGAAAGAGAGAGAG[-/AGAC]AGAGAGAGAGAGAGA | 11060 |
rs745861221 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773376 | TAGAGATTGGGTTTC[A/G]CTATGTTGGCCGGGC | 11060 |
rs745874078 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815279 | AAGTGCTGGGATTAC[C/G]GGCGTGAGCCACCTC | 11060 |
rs745881597 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922375 | TAAAATATTACTGGA[A/C]CTTTGTGCTTAGTTC | 11060 |
rs745896736 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886338 | TGCTTCAGGCTCCCA[A/G]AGTGCTGGAATTAGA | 11060 |
rs745911829 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858612 | CTTCATCTGTTTTTT[C/T]CTTCATGATTGATAT | 11060 |
rs745961162 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803186 | TTATTTTTATTTTCT[C/T]ATTTTTTACTTTTTT | 11060 |
rs745964567 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761002 | CTGTAGTCCCAGCTA[C/G]TCAGGAGGCTGAGGA | 11060 |
rs745984478 | snp | C/T | 4.28366e-05 | 0.00462779 | intron-variant | WWP2 | GRCh38.p7 | 16:69939147 | TCTCTCGCCCTCTGG[C/T]GTCCTGGCTGGCAGT | 11060 |
rs745986193 | in-del | -/C | 4.15822e-05 | 0.00455954 | intron-variant | WWP2 | GRCh38.p7 | 16:69842127 | AAGATCCCGGTAAGA[-/C]CCCCCTTGGTGAGGA | 11060 |
rs745997416 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857069 | AATTTCTGTCTGTCC[C/T]ACAGTTTCTGTTTCC | 11060 |
rs745998313 | in-del | -/GAGTCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781156 | AAAGAACTGAGATGG[-/GAGTCT]GTCTGCACGTTCAAG | 11060 |
rs746010757 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884898 | ATAAATGAAGAAGGT[A/G]TGGTAGAATTAGAAT | 11060 |
rs746038424 | snp | G/T | 1.66749e-05 | 0.00288741 | missense | WWP2 | GRCh38.p7 | 16:69917873 | ACTTCAGCCAAAGAT[G/T]CCTCTACCAGGTGAG | 11060 |
rs746057557 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899552 | CTAGCCAAGATGGTG[-/A]AACCCTGTCTCTACT | 11060 |
rs746068285 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932317 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 11060 |
rs746076520 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804051 | TCATTTTTATATTGA[A/C]GTGTGCATTTTTCTC | 11060 |
rs746100917 | snp | C/G | 1.67259e-05 | 0.00289183 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933084 | CCGCGCCCTGTGTGT[C/G]TCTCTCTCTGTGTCC | 11060 |
rs746104481 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834293 | AGGCATGCTCTCTCA[C/T]CTAGCACCTCTGGGC | 11060 |
rs746111497 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779351 | TGCTCATTAGATCTG[A/G]AACTCCAGACAAAGC | 11060 |
rs746118048 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863609 | TTGCGCCACTTCACT[C/G]CAGCCTGGGTGAAAG | 11060 |
rs746123857 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869795 | TCATCTTGTCAAATT[A/C]TGTTTCTTACTTTAG | 11060 |
rs746131716 | snp | A/G | 1.65332e-05 | 0.00287512 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931837 | TGACCTGCGCCGCCG[A/G]CTCTACATCATCATG | 11060 |
rs746164270 | snp | C/T | 1.7074e-05 | 0.00292177 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931919 | CCCCGGAAGGCTGCC[C/T]TGTACCCCGCTTCCC | 11060 |
rs746169015 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930861 | TGGGTGACAGAGCAA[A/G]ACCCCGTCTCTAGAA | 11060 |
rs746178023 | snp | G/T | 1.66529e-05 | 0.00288551 | intron-variant | WWP2 | GRCh38.p7 | 16:69937268 | TTGCTGGGACCCTGA[G/T]CCCCTGCCTCTGGGG | 11060 |
rs746191287 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822080 | CTTTGTTGCCTGAGC[C/T]GGTCTCAAACTCGTG | 11060 |
rs746206421 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864549 | TGTATAAAAACTCTG[A/T]CCATTCTTTTTGTTG | 11060 |
rs746223579 | snp | A/G | 5.02147e-05 | 0.00501047 | missense | WWP2 | GRCh38.p7 | 16:69871853 | ACCCCAGCAACCGGC[A/G]AGCAAAGCCCCGGTG | 11060 |
rs746234834 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922945 | CCCAGGTTAGAGTGC[A/G]GTGGCGCAATCTCGG | 11060 |
rs746235428 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940488 | GCCTCCCTAGCAGGC[A/G]CCAGCGGTGGAGGCT | 11060 |
rs746263709 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822973 | AAAGCTCCATCTTTA[C/T]TAAAAGTACAAAAAT | 11060 |
rs746270452 | snp | A/G | 1.65258e-05 | 0.00287448 | missense | WWP2 | GRCh38.p7 | 16:69937165 | TGGAAGAGCAGACCA[A/G]AGCCTTCCTGGATGG | 11060 |
rs746275601 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809841 | GGAGAGAGAGAAAAA[C/G]AAAAAAGAAAGAAGG | 11060 |
rs746284328 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853647 | AGGGACTGACGAAGA[A/G]GACTGTTGCAGGAAC | 11060 |
rs746313358 | snp | C/G | 1.65138e-05 | 0.00287343 | missense | WWP2 | GRCh38.p7 | 16:69787067 | TTTTGAGAAGTCTCA[C/G]CTCACTTTGAAAGGT | 11060 |
rs746357426 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811555 | GAGTTTGAGACCAGA[C/T]TCAGTATTGTAGTGA | 11060 |
rs746370325 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841843 | TCCATGGCATGGATC[A/G]GATCCATATGATCGT | 11060 |
rs746379715 | snp | C/T | 4.94279e-05 | 0.00497107 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931227 | CCGTTTCCTCTGCCA[C/T]GTGAGTTCTGGTACT | 11060 |
rs746381758 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889312 | CCTGGACTATGAAGC[A/G]AGACCCCTGTCTCAA | 11060 |
rs746399851 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854366 | GTTTGGTGAGATGAG[G/T]TTCGACTTTTCCTTT | 11060 |
rs746417776 | in-del | -/TCAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883423 | CACACACACACACAC[-/TCAC]ACACTCATTTACTCC | 11060 |
rs746430545 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770132 | CTCCCAAAGTGCTGA[C/G]ATTACAGGTGTGAGC | 11060 |
rs746439395 | snp | C/T | 1.65097e-05 | 0.00287308 | missense | WWP2 | GRCh38.p7 | 16:69935907 | CTCCCTTTCTACAAG[C/T]GGATGCTCAATAAGA | 11060 |
rs746454532 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876369 | GTTTTTTTTTTTTTT[-/C]GTTTTTTGTTTTTGA | 11060 |
rs746476156 | snp | A/G | 6.59761e-05 | 0.00574314 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888196 | GGAACCCAGCACTTC[A/G]GGTACACAGCAGCTC | 11060 |
rs746483888 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842781 | CTCAAGCAATCCACC[C/T]ACCTCAGCATCCTGA | 11060 |
rs746501913 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885717 | GTGCTATATGACCTT[A/G]AGAGGTGTTGTAGCC | 11060 |
rs746503953 | snp | A/G/T | 9.90514e-05 | 0.00703683 | missense | WWP2 | GRCh38.p7 | 16:69787033 | CTGCCAGCTCTAGCC[A/G/T]GGCAGGAGTGGCCCT | 11060 |
rs746530385 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937667 | GGTGGGTCCCGGGCC[A/C]AGGCCTTGGCAGGGA | 11060 |
rs746530540 | snp | A/G | 3.29576e-05 | 0.00405928 | missense | WWP2 | GRCh38.p7 | 16:69930192 | CCAGCGAGGGGGTGC[A/G]ATACTTTGTGGACCA | 11060 |
rs746549139 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789599 | CAGTATTGTTTCTTG[C/T]GTGTCTCTTCCAAGA | 11060 |
rs746555490 | snp | A/G | 1.70339e-05 | 0.00291833 | intron-variant | WWP2 | GRCh38.p7 | 16:69937669 | TGGGTCCCGGGCCCA[A/G]GCCTTGGCAGGGACA | 11060 |
rs746561740 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922249 | GTCTGGTGCATCCTT[-/A]AAAAAAAAAAAAAAT | 11060 |
rs746566200 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873786 | CTTTGTTCTGCCAGA[C/T]GCCTGTGTTATTGAG | 11060 |
rs746611292 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790451 | AGCTGAGGAGGAGGA[A/G]GAAGAGGAAGGATTG | 11060 |
rs746621844 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776551 | TAATGATAATAGGCC[-/G]GGGCGCAGTGGCTTA | 11060 |
rs746625587 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906752 | GGGCCTCGTGGCATG[C/T]ACTTGTTTTCCTAGC | 11060 |
rs746644386 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919043 | GAGATGGGGTTTTGC[C/T]ATGTTGGCCAGGCTG | 11060 |
rs746654340 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883637 | ATCGGTTAAACATGC[A/G]CCATGGTGGTTTACT | 11060 |
rs746671397 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872569 | GGAGGATATCTCATT[C/T]ATACATAGCATATTT | 11060 |
rs746677032 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | WWP2 | GRCh38.p7 | 16:69908772 | TCAGATGGGAACAGC[A/G]AGAGCTGCCCAACGG | 11060 |
rs746684275 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848787 | GTGTGTTTGTGTGTG[A/C]ATGTAGGCCTGGGGA | 11060 |
rs746688258 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915494 | CTGAGGCTGGAGGAT[-/A]GTTTGAGCCCAGCAG | 11060 |
rs746695444 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777540 | TCCTGACCTCAAGCA[A/G]TTCACCCACCTCAGC | 11060 |
rs746697942 | snp | G/T | 1.69066e-05 | 0.00290741 | intron-variant | WWP2 | GRCh38.p7 | 16:69799326 | GGGGTGCCGACGTGA[G/T]TCTTGGGTGGGGATG | 11060 |
rs746726177 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764552 | CATTTTAAGGAAAAA[A/G]ATCACACAGAAAAAG | 11060 |
rs746746967 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819292 | AGAAGTCAAATTGTA[C/T]TGCTACTCCATAAAA | 11060 |
rs746753136 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931597 | TTAGATCATGGTGCC[C/T]GAAACCAGTGGCAGG | 11060 |
rs746798505 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919186 | TTTCTTTTTTTTAAG[A/G]TGGAGTTTTGCTCTT | 11060 |
rs746818608 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916902 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 11060 |
rs746822336 | snp | C/T | 1.65479e-05 | 0.0028764 | intron-variant | WWP2 | GRCh38.p7 | 16:69930105 | GTGGGGCCAGCCCTT[C/T]ACCCTTTTCTTCCCG | 11060 |
rs746843145 | snp | C/T | 3.2981e-05 | 0.00406071 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931514 | TTTTTTTCAGTCAAA[C/T]GCCCTACCTAGCCAC | 11060 |
rs746847152 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820670 | TCTGCTTTATTTTCT[C/T]GTAAGCGGTTCTCCC | 11060 |
rs746852145 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892159 | TGAAACAATGATTCT[C/G]TCTTTTTTTTAATTT | 11060 |
rs746861829 | snp | A/G | 9.88924e-05 | 0.0070311 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936399 | GACCCACGAGCTGAA[A/G]GAGGGCGGCGAGAGC | 11060 |
rs746894539 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867658 | CCTGCCTTCAGGAGG[C/T]CTCAGTTCTTGAGAG | 11060 |
rs746899618 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843838 | AGGGCACTGGGTAAC[-/A]AGAGTGAGACTATGT | 11060 |
rs746911936 | snp | A/C | 1.64787e-05 | 0.00287038 | missense | WWP2 | GRCh38.p7 | 16:69936319 | GCCCCCAGAGAGAAC[A/C]ACCTGGAAGAATGTG | 11060 |
rs746921517 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788370 | TCCTCTGCTCAAACC[A/G]TTCAAGGGTGCTCCA | 11060 |
rs746940182 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902698 | TGACAGAAATATAAC[C/G]TCTGACAGGGATGCG | 11060 |
rs746949967 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838919 | TCTTATTATAATAGA[C/T]CTTTGACTTGATCCA | 11060 |
rs746961480 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878741 | TATTTTGCAGTTAAT[A/G]TTCCATAATTCATCT | 11060 |
rs746968669 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825791 | CCACTACACCTGTCT[A/G]AGTTTTTACATTTTT | 11060 |
rs746999045 | in-del | -/TTAT/TTATTTAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849464 | ACAATGGAATAAGTG[-/TTAT/TTATTTAT]TTATTTATTTATTTA | 11060 |
rs747012689 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882775 | TCTCAAGATGGGTGC[A/G]GTCCTTTTGGGGAGA | 11060 |
rs747018644 | snp | C/T | 3.10989e-05 | 0.00394316 | missense | WWP2 | GRCh38.p7 | 16:69939090 | GTCACCGGTACCTGC[C/T]GCCTGCCCGTCGGGG | 11060 |
rs747029040 | in-del | -/TTTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803308 | GTTAAAACAGGACAT[-/TTTC]TTTATTTTAATTCTT | 11060 |
rs747037650 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901589 | AGCTAATTTTTTTGT[A/G]TTTTGAGTAGAGACG | 11060 |
rs747038894 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813345 | TTTTATATTTTTAGT[A/G]GAGATGGGGTTTCTC | 11060 |
rs747053381 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877652 | CTAAACTTAATAATA[C/T]CTAGTATTTGATTTA | 11060 |
rs747086747 | in-del | -/TTAAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836615 | TAAATTTAAATTAAA[-/TTAAT]TTATTTTTTGAGACA | 11060 |
rs747096825 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772165 | AGGGTTTCATCATGT[G/T]GGTCAGGCTGGTCTC | 11060 |
rs747119186 | snp | A/C | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909506 | GCCACACACATCCCA[A/C]CTCATCTTCTGGTCC | 11060 |
rs747122438 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844181 | CCAGTCATGTTTTCC[A/G]TGTCTCGGTAGGTGA | 11060 |
rs747156634 | snp | A/G/T | 3.39768e-05 | 0.00412158 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931916 | GTGCCCCGGAAGGCT[A/G/T]CCCTGTACCCCGCTT | 11060 |
rs747172682 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812469 | CGCGCCTGCCCCCAA[-/C]CCCCCCCCTTTTTTT | 11060 |
rs747186257 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773145 | AGTCCTGACGGGGAG[C/T]TCCTTCATTGTATTC | 11060 |
rs747206553 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781630 | GCTGGGATTATAGGC[A/G]CCCGCTGGCTTTTAC | 11060 |
rs747206894 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804358 | TTCTGCATCCACATG[A/G]GTTTATTTTTGTGCC | 11060 |
rs747228442 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922547 | CTGGCTGCAGAGTCC[C/T]GCTTTCCCCCATCTC | 11060 |
rs747244483 | snp | A/G | 3.30923e-05 | 0.00406756 | missense | WWP2 | GRCh38.p7 | 16:69937149 | CGTTTCACCCGAGGC[A/G]TGGAAGAGCAGACCA | 11060 |
rs747256796 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896406 | GGTTACAGGTGTGAA[C/T]CACCGTGCCCATCCT | 11060 |
rs747275778 | snp | C/T | 1.67225e-05 | 0.00289154 | intron-variant | WWP2 | GRCh38.p7 | 16:69936479 | GCGCCGGGGGCTCCG[C/T]TCCAGGGGTGGCGTG | 11060 |
rs747295711 | snp | C/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760731 | CTTTGAGGCTAATTA[C/T]GTCATTAGTATTAAT | 11060 |
rs747311038 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791869 | ATGTGAGCCTCTGCA[C/T]CTGTCCAGCACATAC | 11060 |
rs747312873 | snp | C/T | 2.89423e-05 | 0.00380399 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939992 | TAGTCCTGAGTCCTC[C/T]CTGCCTGAGAGGCCA | 11060 |
rs747313043 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803001 | TCAAATAAATACTTA[C/T]GAGACCTGTACAATT | 11060 |
rs747326043 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925579 | TCCCTGTTCCTGTCC[C/T]TCTGTTTTCCATCTC | 11060 |
rs747333975 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833429 | TCTGGTGTGGTGATA[C/T]GTGTTTCCATCAGGA | 11060 |
rs747348365 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870825 | CATTTTCACTGAGTG[A/G]GCAAAGTCAAGCTGC | 11060 |
rs747352861 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906212 | CAAGTAGCTGGGACT[A/G]CAGGTGCCTGCCACC | 11060 |
rs747369807 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905433 | AATGTCTGTGGACCC[A/G]TTACAGGTTGAGTGT | 11060 |
rs747378917 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902903 | TTGTGTGAATTATGA[A/G]TAGCCATGCAGGTGA | 11060 |
rs747380914 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927859 | TAGAGATGAAGTCTC[A/G]CTGTGTTGCCCAGGC | 11060 |
rs747381256 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862292 | CAGGTCTGGAAGTCC[C/T]GACCTCAGGTGATCC | 11060 |
rs747390758 | snp | C/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942042 | GGTGCAGAACAATAA[C/G]AGCTACAGACTGGGT | 11060 |
rs747402842 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792609 | CCTGGCCAACTCCAC[A/G]TTAAGCAGATGTTCA | 11060 |
rs747404291 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863511 | GGGCGAGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 11060 |
rs747421802 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821240 | CCAAAGATGCCAAAA[A/G]CAACCCCCTCCCTCA | 11060 |
rs747424429 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779428 | TTTTAAAAGACACTG[A/G]AGAAAGAAAACATGG | 11060 |
rs747427596 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850695 | GAACTTGATGTATTT[A/G]AGGAAATAAAAGTCA | 11060 |
rs747443360 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780465 | GGCCTCTTCTGTGTG[G/T]GTTGGAGAATTTCTC | 11060 |
rs747467972 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809003 | TACTGTGCTCTGATC[A/G]TTTGTAATTACTGTT | 11060 |
rs747476794 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941393 | TCCCCCGGCCCGGGA[A/G]GTGCAGCCTGCGTCT | 11060 |
rs747490989 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935134 | AGGCACAGCGCGGGA[A/G]CCACATGCATAGCTG | 11060 |
rs747502315 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821725 | TCTTTTCTTTCTTAC[-/TTT]TTTTTTTTTTTTTTT | 11060 |
rs747508147 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821890 | TTTTTTTTTAAATAA[C/G]AAACAGGGTCTTACT | 11060 |
rs747523439 | in-del | -/GCTGCCCAGGCCCCCGACGCTCTGCCT | 1.66084e-05 | 0.00288165 | cds-indel | WWP2 | GRCh38.p7 | 16:69888218 | CAGCAGCTCCCAGCG[-/GCTGCCCAGGCCCCCGACGCTCTGCCT]GCTGGGTGAGTAGTC | 11060 |
rs747569170 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864238 | CTGGACATGGTGGTG[C/T]GCACCTGTGATCCCA | 11060 |
rs747581228 | snp | C/T | 1.67396e-05 | 0.00289301 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871849 | AACAACCCCAGCAAC[C/T]GGCGAGCAAAGCCCC | 11060 |
rs747593922 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928052 | AAATTTCAGTCGAGT[C/T]ATAGATACCAGGTAA | 11060 |
rs747608065 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781457 | CTCAAGGGATCCTCC[C/G]AACTCTGTGGTCCTG | 11060 |
rs747627842 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853549 | GGGTCTGGAAGTCTT[C/T]TAGGCCCTGCAGTGC | 11060 |
rs747632450 | snp | C/T | 0.000115882 | 0.007611 | intron-variant | WWP2 | GRCh38.p7 | 16:69937545 | ACTGCCGCCTCTCCC[C/T]AGCTGATGCTGTGCG | 11060 |
rs747638715 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809581 | AGACCAGCCTGACCA[A/G]CATGGTGGAACCCTG | 11060 |
rs747654649 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890563 | GAACAATGCAGAATC[A/G]TGTTGGCAGAAAGGA | 11060 |
rs747677703 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926961 | CCCAGTCAAGTGGGT[A/T]TTCATGCCAGTTCTG | 11060 |
rs747708870 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899628 | TCAGCTACTCGGGAG[A/G]CTGAGGCAGGGAATT | 11060 |
rs747744217 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828823 | CTCTTCTTCCATGAT[C/T]TCATCTCTGTTTCAC | 11060 |
rs747759717 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829528 | ATTGTGCCACAGGAC[C/G]TTTGCACACAACATT | 11060 |
rs747764450 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833883 | CTGCGGGGCCTGGCT[C/G]ATGTGCTCGGTGGGG | 11060 |
rs747801009 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908304 | TGGGTAGACGAAAAA[A/G]CCTGGAGGGCCTATA | 11060 |
rs747824412 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859023 | TGTATTTGAGAGTTC[C/T]ATCTTCTACTGTGGA | 11060 |
rs747847830 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888166 | CCCTGCCCCAGCCAC[A/G]CCGGCTGAAGGAGAG | 11060 |
rs747854529 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811522 | GGAGGCTGAGGTGGG[A/T]GGCCCTCTTGAGCCT | 11060 |
rs747893274 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935326 | GAAATGGGCACATTC[C/T]TCCCAGGTCTAGAGA | 11060 |
rs747897011 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907593 | CTTTATATATAGGTT[A/G]CTATATTCTGGGTAA | 11060 |
rs747899260 | snp | G/T | 1.64914e-05 | 0.00287149 | intron-variant | WWP2 | GRCh38.p7 | 16:69936292 | TAGACATCTCCCCAC[G/T]TGGTCTCCTGTGCCC | 11060 |
rs747924293 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931251 | TGGTACTGGGGCTCC[C/T]GTGGCAGTTGGGGTT | 11060 |
rs747926257 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830463 | TGTAAAAATGAGGCT[A/G]TTTTCTCTAGAAGAG | 11060 |
rs747946536 | snp | A/G | 5.01098e-05 | 0.00500524 | missense | WWP2 | GRCh38.p7 | 16:69888225 | TCCCAGCGGCTGCCC[A/G]GGCCCCCGACGCTCT | 11060 |
rs747991829 | snp | A/T | 1.65089e-05 | 0.00287301 | missense | WWP2 | GRCh38.p7 | 16:69935965 | TTGACCCTGAGTTCT[A/T]CAACTCCATTGTCTG | 11060 |
rs747994981 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845383 | GATGAATCAGACCTT[C/T]GGGATCAAGGGCAGT | 11060 |
rs748006573 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855519 | TGATTTTTATTACTT[-/A]AAAAAATGAGTTTGA | 11060 |
rs748010595 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919314 | GGGATTACAGGCACA[C/T]GCCACCGTGCCTGGC | 11060 |
rs748015841 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918011 | ACGTCAGTGCTCTGC[C/T]CCTGGAGATTTTACT | 11060 |
rs748064420 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805591 | ATTAATCATTGCAGG[C/T]TAAAAAAAAAGTCAG | 11060 |
rs748064720 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | WWP2 | GRCh38.p7 | 16:69840119 | TGTTGCCTTTTGTAC[C/T]CCACAGTGGAGAACA | 11060 |
rs748068111 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794078 | GTGCGCCACCACGCC[C/T]GGCTAAGTTTTGTAC | 11060 |
rs748082528 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893298 | GCACACCAAGGTGGC[C/T]GGGAGCCTGGCACAG | 11060 |
rs748103425 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930464 | GCCTGGACAACATAG[C/T]GAGACCGTGTCTCCA | 11060 |
rs748122425 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868542 | CAGCTTGCTCCTGGG[A/G]GCTGCAAGTTCCAAA | 11060 |
rs748126142 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903194 | ATCAAAGATGGAAGG[G/T]TGGGCCTTATCTGGG | 11060 |
rs748127945 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824902 | CAGCCTCCCAAGGAG[C/T]TGGGATTACAGGCAT | 11060 |
rs748141348 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919032 | ATTTTTAGTAGAGAT[-/G]GGGGTTTTGCCATGT | 11060 |
rs748150237 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940125 | AGTTCCCCCGACCCG[C/T]GGATGGCAGTCTGGA | 11060 |
rs748159090 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922185 | TTTCTTACTCTGCAA[C/T]GAGCCCCTTGCATTG | 11060 |
rs748174440 | snp | A/G | 1.65419e-05 | 0.00287588 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931805 | CTGTCTTCCCAGATC[A/G]TGAACATGAAACCCT | 11060 |
rs748175535 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838446 | GACCCTCCTTGACTT[-/AAA]AAAAAAAAAAAAAAA | 11060 |
rs748177518 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788179 | ACCAGCCTGAGCAAC[-/AG]AGCAAGACCCCCGTC | 11060 |
rs748190138 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823210 | ACATATCTGAAATGC[G/T]ATTTTAACATGTAAT | 11060 |
rs748219599 | snp | A/G | 4.5045e-05 | 0.00474558 | intron-variant | WWP2 | GRCh38.p7 | 16:69871947 | GTGAGTGATGGCACC[A/G]CACGCCAGCCTGCAC | 11060 |
rs748278176 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895944 | TTTGTGACTCTGCAG[A/G]GATTGTTACATGCTT | 11060 |
rs748278312 | in-del | -/CTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817659 | ACTTTTTGTTAAACT[-/CTTTTTTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs748287792 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825525 | GTCATAGTTTACCTT[G/T]CTGTATTTGAATTTT | 11060 |
rs748293702 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770367 | ATCATGCCTGCGTAA[G/T]GAAGCTTCCATAAAA | 11060 |
rs748296844 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902792 | GAGGCTCCATCTATG[G/T]GAGTCAGCGGCCACT | 11060 |
rs748307426 | snp | A/C | 0.000443489 | 0.0148845 | missense | WWP2 | GRCh38.p7 | 16:69888056 | AATGATGAACCCACA[A/C]CAGCCACTGATCCCG | 11060 |
rs748356463 | snp | A/T | 1.64836e-05 | 0.0028708 | missense | WWP2 | GRCh38.p7 | 16:69936412 | AAGGAGGGCGGCGAG[A/T]GCATCCGGGTCACAG | 11060 |
rs748356871 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826725 | TCTAATAAAAATACA[-/AA]AAAAAAAAAAAAAAT | 11060 |
rs748359354 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760472 | TACCTGGGATTACCC[A/G]CACCCGGACCATGCC | 11060 |
rs748383086 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843241 | CCTTGTAATGTTGGT[G/T]AAGACCTCCTACGCT | 11060 |
rs748384791 | snp | A/G | 3.37564e-05 | 0.00410817 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939895 | ACAGCTGAGAGAGAA[A/G]CTGCTGTATGCCATT | 11060 |
rs748390404 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877856 | GCTGTTGCCCACGCT[A/G]GAGTGCAATGGCATG | 11060 |
rs748391520 | snp | G/T | 2.45546e-05 | 0.00350381 | intron-variant | WWP2 | GRCh38.p7 | 16:69939803 | ATCAGAGCCCTGGCC[G/T]CCTAGGGCTGACTGT | 11060 |
rs748402667 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763133 | TTTTAGCTTACACTG[C/T]TGACCTAGCCCAGCG | 11060 |
rs748417497 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856158 | AAAGTAACTTAACAA[C/T]GTGAATGACTCTTAA | 11060 |
rs748420287 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887171 | GTGTGTTTCACTTCT[A/G]TCTCATTGTCTATTA | 11060 |
rs748461619 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924249 | GCTGTGGAAGGGGGC[G/T]TGCTGGCAGTTGAGT | 11060 |
rs748468320 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772076 | GCTATTCTCCTGCCT[C/T]GGCCTATCCCAAGTA | 11060 |
rs748489006 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800308 | TTCTGAATTGGTGTT[C/T]ATTTTCCCAAACCCT | 11060 |
rs748493826 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802091 | CCCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 11060 |
rs748505018 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897052 | TACCTGTGGCTCATC[A/G]TCTTTGGCTCTGTGC | 11060 |
rs748506233 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | WWP2 | GRCh38.p7 | 16:69934090 | CATCAACCCGGACCA[C/G]CTCACCTACTTTCGC | 11060 |
rs748510267 | in-del | -/C | 6.26782e-05 | 0.00559778 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933033 | TTTCCGTGGTGACCT[-/C]CTCTCCAGGCTCTGC | 11060 |
rs748526768 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778705 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 11060 |
rs748541805 | in-del | -/G | 1.64871e-05 | 0.00287111 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908865 | GGTAGGTCATCAACT[-/G]AGAAGACCTGAGACT | 11060 |
rs748546013 | snp | A/G/T | 4.95572e-05 | 0.0049776 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908895 | TCTGGAACTGACACC[A/G/T]TGAGTCACCCAATGG | 11060 |
rs748549161 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | WWP2 | GRCh38.p7 | 16:69917749 | GGCAGGTTTTACTAT[A/G]TGGATCACAATACTC | 11060 |
rs748549444 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922783 | AGAAGTATCCAAAAT[C/T]GTCAAGTGCTTCTAT | 11060 |
rs748560986 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831337 | ATAATGAGAAAATAC[C/T]CCAAACTAGAAAGTT | 11060 |
rs748578972 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790757 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTT | 11060 |
rs748585763 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791782 | ACCTTGGCCTCTTAA[A/G]GTGCTGGGATTACAG | 11060 |
rs748621512 | in-del | -/ATCACAAATGTTCTTAATGGC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875894 | GACCTCCTCCCATGA[-/ATCACAAATGTTCTTAATGGC]ATCTAGAATGGTGAG | 11060 |
rs748637298 | snp | A/G | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933462 | GGCAGCATGGATTAC[A/G]TTGTCATGGATCGGG | 11060 |
rs748650942 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833206 | CCAAACAAGATTGAT[A/G]TATCTTTTCAGTCTC | 11060 |
rs748688640 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862156 | CTGCAACCTCAGCCT[C/T]CAGGGTTCAAGTGAT | 11060 |
rs748705670 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871021 | CCAGGCATAGTGGCT[C/T]ATACTTGTAATCCCA | 11060 |
rs748724347 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779245 | CGTGAGCCACTGTGC[A/G]TGGCCCCGGCCGGTT | 11060 |
rs748736570 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905601 | ATCTGAAAACAAAAA[A/G]TCCAAAATCTGAAAC | 11060 |
rs748748471 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942145 | AGTTCCACGACGGTC[A/G]AGGGACTCTGTGATC | 11060 |
rs748773500 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801144 | CAGTGAGCCGAGATT[A/G]CGCCACTGCACTCCA | 11060 |
rs748777832 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924588 | AATTTGGCTGGAGGG[G/T]GTGTGGGGGGGATTC | 11060 |
rs748779753 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845840 | AGATCACTTGAGGTC[A/T]GGAGTTTGAGACCAG | 11060 |
rs748783689 | snp | A/G | 3.30142e-05 | 0.00406276 | intron-variant | WWP2 | GRCh38.p7 | 16:69840273 | CAGATGGTGAGTGCC[A/G]CCCTGCTCCTCAGGA | 11060 |
rs748785915 | snp | C/T | 3.30006e-05 | 0.00406192 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917745 | CCGAGGCAGGTTTTA[C/T]TATGTGGATCACAAT | 11060 |
rs748804597 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881169 | CTTTCCCTCCTTGGT[A/G]CCCCACTTTCCCGGT | 11060 |
rs748812131 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780381 | ATCCATTCCCCCATT[A/G]ATGGGTATTTAAGTT | 11060 |
rs748828761 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915541 | GCAACATAGTGAGAT[C/T]CTGTCTCTGTATTAA | 11060 |
rs748833983 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900201 | GAAAAATAATTAAAC[A/G]GTATTCACATAATAA | 11060 |
rs748858375 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891283 | GGTTATTAATTTACC[C/T]CTGGTGTTCCAGAGT | 11060 |
rs748868634 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852058 | ACATGATTGCTGGGT[C/G]ATATGGTAAAAGTAT | 11060 |
rs748870094 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928198 | TCTGGTTCCCTGTAG[C/T]TTCTGGAACTGATTA | 11060 |
rs748888387 | snp | C/T | 1.64925e-05 | 0.00287158 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935939 | ACCAACCCTGAAAGA[C/T]CTGGAGTCCATTGAC | 11060 |
rs748891429 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839522 | TGGGGACGGGGTGCT[C/T]TGGGCCACTTCTCAA | 11060 |
rs748893708 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771701 | TCTCTTTTTCTCTCT[A/G]TTTGTTTTTATATCT | 11060 |
rs748898465 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840328 | GGCGGGGGCCAGGAG[A/G]TGCTGAGAGCTTGGT | 11060 |
rs748950422 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890714 | GTCTTTATGTAGGGC[A/G]TGTGTGAGGGTTACT | 11060 |
rs748961907 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936878 | CTGAGGTTCAGTCGG[C/T]GCTGGGGGCAGGAGC | 11060 |
rs748965006 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931144 | CTGAACATCTTTGCT[C/T]TTCCTAGGACGAAGC | 11060 |
rs748988673 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828748 | TCAGGTGATCCACCC[A/G]TCTTGGCAAGGTCAT | 11060 |
rs748999075 | snp | G/T | 1.65059e-05 | 0.00287275 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929470 | ACAGGACAATGGACG[G/T]GTGTATTACGTGAAC | 11060 |
rs749025996 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797956 | CTCCTGGGCTGAAGC[A/T]GCCCTCCCACCTTGG | 11060 |
rs749027951 | snp | C/G | 3.31669e-05 | 0.00407215 | intron-variant | WWP2 | GRCh38.p7 | 16:69786983 | TGAATTCTTTTTTCT[C/G]TTTGTCTTACAGCTT | 11060 |
rs749029934 | snp | A/C | 0.000765667 | 0.0195511 | intron-variant | WWP2 | GRCh38.p7 | 16:69939133 | TCATCGGTATGTTTT[A/C]TCTCGCCCTCTGGCG | 11060 |
rs749052862 | snp | A/G/T | 0.000222173 | 0.0105379 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935855 | TCTTCCTTCCCAGGC[A/G/T]CTGTACCATGGAAAG | 11060 |
rs749055347 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876483 | GATTCTTGTGCCTCA[G/T]CCTCCAAAGTAGCTG | 11060 |
rs749121607 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936176 | ACCTTCTCCTTGAGT[C/T]AAGGAGCTGTCCCCT | 11060 |
rs749149864 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908415 | TCCTCAGCTTTCATC[A/G]TGTTCCTAAAGGGAC | 11060 |
rs749162563 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806945 | TCTGTTTTATTTATT[C/T]ATTTATTTATTCATT | 11060 |
rs749170429 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907665 | GGGATAAGTGGTCCT[C/T]GGCTGTATTTTGTAC | 11060 |
rs749179461 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880530 | CATCTGTATATACAC[C/T]GGGGAAGGATTTTAC | 11060 |
rs749179480 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902136 | CAACGGGTAATTGAG[C/T]ATTAATTTCCTGAAG | 11060 |
rs749187424 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825884 | TCACCTTGGCCTCTC[C/T]AAGTGTTGGGATTAC | 11060 |
rs749190953 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884815 | CTGCCTTTTCTTTAC[A/G]AACTGAACCTCCAGG | 11060 |
rs749192267 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | WWP2 | GRCh38.p7 | 16:69888149 | CCCAACACGACTTCT[C/T]TCCCTGCCCCAGCCA | 11060 |
rs749197211 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859779 | GTGATTTGAATCTCT[C/G]TGATTTTCTCTCCTG | 11060 |
rs749209924 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803374 | CATTTACATAAAAAA[A/T]ACATTATCTTACACA | 11060 |
rs749215554 | snp | A/C/T | 0.000132722 | 0.00814522 | missense | WWP2 | GRCh38.p7 | 16:69888216 | CACAGCAGCTCCCAG[A/C/T]GGCTGCCCAGGCCCC | 11060 |
rs749221247 | snp | C/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69775113 | ATCGTGGAGAAATAC[C/G]ATTGGACAAAAGGGG | 11060 |
rs749226026 | snp | A/G | 3.38518e-05 | 0.00411397 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931908 | GAGCTTGAGTGCCCC[A/G]GAAGGCTGCCCTGTA | 11060 |
rs749260362 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919541 | ACAGTCTCCTATACC[A/G]TGTCCCTGTGGGAAC | 11060 |
rs749280832 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894568 | TTTTAAATTAACTAG[C/T]GTGAAAGAAGCCAAC | 11060 |
rs749282458 | snp | A/T | 1.65825e-05 | 0.00287941 | missense | WWP2 | GRCh38.p7 | 16:69799190 | AATGTCACGGCACAG[A/T]GTCATTTAGATTTAA | 11060 |
rs749287202 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848589 | CTATAGTGAGCCAAG[A/G]TGGAGACCCTGCAAT | 11060 |
rs749297655 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804189 | AACTTTCTGTAGTCC[A/G]ATCTGTCACCCTTTA | 11060 |
rs749314438 | in-del | -/CACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912370 | GCAGGGAGTTAGATT[-/CACACACA]CACACACACACACAC | 11060 |
rs749326066 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925430 | GTTTCTTGTGTTTAG[A/T]CTTCGAGTGCTTCGA | 11060 |
rs749338277 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763975 | CTTCTCAGTCTCTTT[C/G]ACTTCATGATTACTT | 11060 |
rs749380598 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930391 | CCCTCTAGTGGCCAA[C/T]GTTGATGTCATATTA | 11060 |
rs749386001 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799615 | ATGTTGAATGAAACT[A/G]TCAAATACCTCTAGC | 11060 |
rs749403541 | snp | C/G | 1.64874e-05 | 0.00287113 | intron-variant | WWP2 | GRCh38.p7 | 16:69939790 | GCATGGTGGGGCTAT[C/G]AGAGCCCTGGCCTCC | 11060 |
rs749415882 | in-del | -/CCCG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878052 | ACCTCAGGTGATCCA[-/CCCG]CCTCAGCCTCCCAAA | 11060 |
rs749418137 | snp | A/T | 1.64776e-05 | 0.00287028 | missense | WWP2 | GRCh38.p7 | 16:69936329 | AGAACAACCTGGAAG[A/T]ATGTGGCCTGGAGCT | 11060 |
rs749421217 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904491 | CTCCTGCCTCAGTCT[C/T]CTGAGTAGGTACGAT | 11060 |
rs749426724 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893480 | AGGGCAAGAAAGTTG[A/G]GCCTAATGCTGTCAT | 11060 |
rs749433267 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786556 | CCTGGGCTCAAGTGA[-/T]TCTCCTGCCTCAGCC | 11060 |
rs749444637 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864950 | AGATATGTAATGATA[C/T]CTCATTGTAGTTTTA | 11060 |
rs749472010 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820352 | GTTCAAGTGATTCTC[C/T]TGCCTCCGCCTCCTG | 11060 |
rs749493460 | snp | C/G | 1.64936e-05 | 0.00287168 | missense | WWP2 | GRCh38.p7 | 16:69939372 | GAAGTTTTGCATTGA[C/G]AAAGTTGGCAAGGAA | 11060 |
rs749509109 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903423 | AAATGAACATAAAAG[A/C]TGTCAAAAGTGGAGA | 11060 |
rs749522041 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835866 | GGAATGTGGTGGCAC[G/T]ATCCTGGCTCCCTGC | 11060 |
rs749534450 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865522 | CTAAAGGGGGGGTAC[A/C]ATAACCTGCAGGCAG | 11060 |
rs749539069 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879828 | TTATCTGTTACATTT[A/G]TAAGTTTTCCCATAT | 11060 |
rs749559509 | snp | A/G | 4.15904e-05 | 0.00455999 | intron-variant | WWP2 | GRCh38.p7 | 16:69871939 | TGGCACAGGTGAGTG[A/G]TGGCACCGCACGCCA | 11060 |
rs749580186 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879112 | TTGTGTCTCTTTTCA[C/T]AGTATTTGATCATTT | 11060 |
rs749595930 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783219 | TTCATCACATTGGCC[A/G]GGTTGGTCTCAAACT | 11060 |
rs749606608 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811639 | TGCAACGGTAGTCCC[A/G]GCCACTTGGGAGGCT | 11060 |
rs749620778 | snp | A/C | 3.87529e-05 | 0.0044017 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933212 | TCCTCGTCTGCCCAG[A/C]CACAAACAGCCCAGC | 11060 |
rs749631853 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940140 | CGGATGGCAGTCTGG[A/G]ATAAAGCCCCCTAGT | 11060 |
rs749633432 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887728 | ATTCCTGTTATGTTG[A/C]TCTTTCCTGCTACTC | 11060 |
rs749636126 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889736 | TTTTCACTGCCTCTC[C/G]TGGTTATCAGTTTGG | 11060 |
rs749644279 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813004 | CCTATAGATTTTTAT[A/T]TTTGAATTCCATCCT | 11060 |
rs749648257 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925892 | GTTGGAATGATCCAC[C/T]CTAACAAATCTTTCT | 11060 |
rs749653795 | snp | G/T | 3.31535e-05 | 0.00407132 | intron-variant | WWP2 | GRCh38.p7 | 16:69937521 | GGGAGGGACCTGCCG[G/T]GGATGCTGACTGCCG | 11060 |
rs749676230 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842911 | TGGACTCAACCGATT[C/G]TCCTGTCCTGGCCTC | 11060 |
rs749726025 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937739 | TCACGCGCAAGGACC[-/T]TTCAGCTTTGGCCCT | 11060 |
rs749740379 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854723 | GCCTGGATAATTTTT[G/T]TATTTTTAGTAGAGG | 11060 |
rs749768227 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830693 | CAACAGGAATACCAG[A/T]GTTCACTGTTGGCCT | 11060 |
rs749779117 | in-del | -/GAGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877730 | AATGTAGGGTATAAG[-/GAGA]GAGAGAGAGAGAGAA | 11060 |
rs749781299 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924432 | ATAAAAATGCTTCAG[A/G]AAGAAAAAAAAGAAA | 11060 |
rs749787204 | snp | C/T | 1.67621e-05 | 0.00289495 | intron-variant | WWP2 | GRCh38.p7 | 16:69937284 | CCCCTGCCTCTGGGG[C/T]GATCCTGCTCTGTGA | 11060 |
rs749793847 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897185 | TCAGCTCACTGCAGC[C/G]TTGACCTCCCAGGCT | 11060 |
rs749835553 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873449 | ACTGACTAGCCCACC[C/T]TGAGCCTTGGGGAAG | 11060 |
rs749836760 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814432 | CACTCTCATGAGAAC[C/G]CTGGCACTCAACACT | 11060 |
rs749844853 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918948 | TCCTAGGTTCAAGCA[A/G]TTCTCCTGCCCCAGC | 11060 |
rs749851086 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant | WWP2 | GRCh38.p7 | 16:69939294 | AGGATCCTGCTTTGG[A/G]AAGGGACGTCTCTGC | 11060 |
rs749856534 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790678 | TCTCCTGGGTTCAAG[C/T]GATTCTCATGCCTCA | 11060 |
rs749887982 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875195 | TGCATATAAAAGTTA[C/T]GTTTACACTATACTA | 11060 |
rs749891362 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844506 | AAGTCAGATTCAGCT[A/G]TTAACAAGTTTGGAT | 11060 |
rs749901201 | snp | A/G | 1.65015e-05 | 0.00287237 | missense | WWP2 | GRCh38.p7 | 16:69935917 | ACAAGCGGATGCTCA[A/G]TAAGAGACCAACCCT | 11060 |
rs749921377 | snp | G/T | 1.65081e-05 | 0.00287293 | stop-gained | WWP2 | GRCh38.p7 | 16:69798801 | CGCATTGGGAGCTCT[G/T]AGCTTCTCTGGAATG | 11060 |
rs749924743 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802793 | ATTTTTAGTAGAGAC[A/G]GGAGTTTCACCATGT | 11060 |
rs749927890 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824769 | TTTGCACCTGTGGCT[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs749943045 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852220 | TTGGCTATTCTAATG[-/T]GGTATCTAGTGATAT | 11060 |
rs749971534 | in-del | -/TTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866279 | TTCACATTTTATTTA[-/TTTA]TTTATTTATTTATTT | 11060 |
rs749979312 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845532 | TATTCACTGTGATCA[A/G]ACAAAGGTGCTCTGA | 11060 |
rs749980432 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69931027 | TCTTAATGACAGTCA[C/T]TTCCTCACCTTACAT | 11060 |
rs749992969 | snp | A/C | 3.4093e-05 | 0.0041286 | missense | WWP2 | GRCh38.p7 | 16:69939116 | CGGGGGATTTGCCGA[A/C]CTCATCGGTATGTTT | 11060 |
rs749994228 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868662 | ACACATACACATGTG[-/CA]CACACACACACACAC | 11060 |
rs750011355 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892945 | TCCTTAATAAGGCCT[A/G]AAAAGGCCTGTGTAA | 11060 |
rs750013131 | snp | C/G | 1.71076e-05 | 0.00292464 | intron-variant | WWP2 | GRCh38.p7 | 16:69799123 | AATGTTTTCTTCTAA[C/G]TTATAGGAATGATCT | 11060 |
rs750027527 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761439 | TTAGCCAGGCGTGGT[A/G]GTGCACGCCTGTAAT | 11060 |
rs750036954 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895201 | TAAGAGATGTTGGAA[-/T]TTGGAGCTTCTCTGC | 11060 |
rs750076266 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939754 | AGTGTGGTGCAAGCC[C/T]TGTGGCCCTGCTGCA | 11060 |
rs750077025 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833875 | CAGTGGCCCTGCGGG[A/G]CCTGGCTGATGTGCT | 11060 |
rs750101743 | snp | C/T | 1.73896e-05 | 0.00294865 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931939 | CCCCGCTTCCCCAGG[C/T]TACAGCATCAATGGC | 11060 |
rs750103007 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849882 | TCAATTAAAATGATA[-/C]ATGGTACCTTATTAT | 11060 |
rs750108500 | snp | A/G | 6.61649e-05 | 0.00575135 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917724 | CTGGGAAAAACGCAC[A/G]GATCCCCGAGGCAGG | 11060 |
rs750121823 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879399 | ACCTGACCGGCCCCC[A/G]CCCACAGCCCATGGT | 11060 |
rs750137550 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780161 | CGTACTTTTATACTT[C/T]TAAACGTTTGTGTGT | 11060 |
rs750146909 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863910 | TATTCCTTTTATGCA[C/T]TGAGTTTATTCCACT | 11060 |
rs750161159 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878412 | GGTATGCCTGTATAT[A/T]AAACATGCAGAGTGT | 11060 |
rs750164467 | snp | G/T | | | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939095 | CGGTACCTGCCGCCT[G/T]CCCGTCGGGGGATTT | 11060 |
rs750167064 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821655 | TTCTACAGGTATATT[C/G]TGACTGTTTGCATTT | 11060 |
rs750181767 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907235 | ACTGAGGAGGTTGCT[A/G]GATGCCTGTGGGTTT | 11060 |
rs750211901 | snp | A/G | 5.57502e-05 | 0.00527939 | missense | WWP2 | GRCh38.p7 | 16:69842050 | CCTTCGAGAGACTCC[A/G]GTGGAACAGCAGTAG | 11060 |
rs750253078 | snp | G/T | 2.01359e-05 | 0.00317294 | missense | WWP2 | GRCh38.p7 | 16:69842120 | TTGGTGGAAGATCCC[G/T]GTAAGACCCCCCTTG | 11060 |
rs750256038 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910296 | CCCAGTCAATATTTG[A/G]CTTTCTATAATTGTG | 11060 |
rs750267889 | snp | A/G | 3.42536e-05 | 0.00413831 | intron-variant | WWP2 | GRCh38.p7 | 16:69937081 | ACCCCTGAGCAGTGG[A/G]TCTCAGACTCCACCC | 11060 |
rs750284154 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768785 | GGGGCTTCCAATAGT[A/G]TACCTCCCTGCTCCC | 11060 |
rs750287153 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777178 | CATATGGATATACAC[-/A]TATGTGTATATACAA | 11060 |
rs750343549 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923906 | ACCCTATCTCCCCCA[A/G]CCCCCCAACACACAG | 11060 |
rs750351965 | snp | C/T | 2.03461e-05 | 0.00318946 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939950 | GAGTAACCGAGGCCG[C/T]CCCTCCCACGCCCCC | 11060 |
rs750354017 | snp | A/G | 3.33806e-05 | 0.00408524 | intron-variant | WWP2 | GRCh38.p7 | 16:69936471 | AGTCTCAGGCGCCGG[A/G]GGCTCCGCTCCAGGG | 11060 |
rs750360147 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841262 | GTGATTGTAACAAAA[C/G]CTATCAGTGAAAACC | 11060 |
rs750367617 | snp | A/C/G | 0.000199617 | 0.00998863 | intron-variant | WWP2 | GRCh38.p7 | 16:69929549 | GGACTTGGGCTGAGA[A/C/G]GGGGGCCGGGCTGGG | 11060 |
rs750375020 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778255 | GGGGGACATTTTGAC[-/T]TTCCCATCCCCCTCC | 11060 |
rs750385696 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886943 | CTAAGGTGTTTTCCT[A/G]TGAATTTCTAGTATA | 11060 |
rs750395353 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896863 | GCTACTTTTATCCTC[A/T]TCTTGCAAGTGAGGA | 11060 |
rs750445855 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842227 | GAAACTGTTGGAGAT[C/T]TCCAGAGATCTTGTA | 11060 |
rs750449137 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933815 | ACTGACCAGCTGTTC[A/T]TATAGGTTAGCCCGG | 11060 |
rs750497012 | snp | A/G | 4.94947e-05 | 0.00497443 | intron-variant | WWP2 | GRCh38.p7 | 16:69908723 | GGCCTATGCCTTTCC[A/G]CTGTGTGTCTCATGC | 11060 |
rs750515642 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900992 | GATTTAAAGGCTAGT[C/T]CCTTATTTCAGGAAG | 11060 |
rs750518447 | snp | A/C | 1.95383e-05 | 0.0031255 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933198 | CTGCGTCGACGGACT[A/C]CTCGTCTGCCCAGCC | 11060 |
rs750532036 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789250 | TGTTTGTTTTTTTGA[A/G]ATGGAGTCTCGCTCT | 11060 |
rs750535247 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830276 | TTTTCTGTTTTATAG[A/C]GATGAGGGTCTCACT | 11060 |
rs750544305 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816899 | ATGAAGAAATTGAGG[G/T]GGAGAGATGCTATGT | 11060 |
rs750573809 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789925 | TAATAGCCTGCTGTT[A/G]ACTGAAAGCCTTGCC | 11060 |
rs750574470 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870616 | ACCTTTATTGTTGAG[A/G]GTAGTTTTATCGCCC | 11060 |
rs750575390 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906166 | CAAGCTCCGCCTTCC[A/G]GGTTCACGCCATTCT | 11060 |
rs750577791 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942002 | CCGCCTGCTGGACCC[A/G]GGGGTCTCCAAGCAG | 11060 |
rs750599740 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827318 | AATAGGGTGCATTCT[A/G]TAATGTCAGAGGTTG | 11060 |
rs750623601 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776112 | TCTATAGCCTCATGG[C/T]CAAATCCTAGTCTTT | 11060 |
rs750631683 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770629 | CCTCGATTTATAGCC[A/G]GTTGGTCAGAAGCAC | 11060 |
rs750664599 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776962 | CCTTAGATGGGATTG[C/T]TGTAGACCAGTAGTC | 11060 |
rs750671305 | snp | A/G | 6.63493e-05 | 0.00575936 | intron-variant | WWP2 | GRCh38.p7 | 16:69937510 | GACGATGCGCGGGGA[A/G]GGACCTGCCGGGGAT | 11060 |
rs750677116 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805224 | TATTTTTGGTAGAGA[C/T]GGGGTTTCATCATTA | 11060 |
rs750680120 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763768 | TATTTGGCTGCTAGC[C/T]TAGTGCCTGGCATGT | 11060 |
rs750686038 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772930 | CAAAATTTTGCTGCT[C/G]TTTCCGTTGTGTTTT | 11060 |
rs750686648 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909083 | GGGAGGCCAAGATTT[-/AG]AGTGTTGATGCATTC | 11060 |
rs750693034 | in-del | -/GGGGGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917656 | GACTTTTCTAGAATT[-/GGGGGA]TGGGAGTGGGGTGGT | 11060 |
rs750726951 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929145 | TATGCCTCTGGTTTG[A/C]GCTGTGCTGCTCCCT | 11060 |
rs750742176 | snp | C/G/T | 3.298e-05 | 0.00406068 | intron-variant | WWP2 | GRCh38.p7 | 16:69925513 | TCTCTTCCTGGCCCT[C/G/T]GGCCTTCCGTCAGCC | 11060 |
rs750753479 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931543 | ACGTGAAGATCAGCG[C/T]TTCCAGGCAGACGCT | 11060 |
rs750769732 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765038 | GTGAAACCCTGTCTC[C/T]ACAAAAAATACAAAA | 11060 |
rs750787678 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913113 | CACTGCAACCTCCAC[C/G]TCCCAGGTTCAAGCG | 11060 |
rs750840790 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893437 | AAAGAAAGAACAGCT[A/G]TGACAGCAATATTGC | 11060 |
rs750843156 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915187 | AAACCACACAGAAGA[C/T]GACAAGGAAGTTCTC | 11060 |
rs750856072 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900712 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 11060 |
rs750890385 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859437 | GCGCATGCCTGTCAT[A/C]CCGGTTACTCAGGAG | 11060 |
rs750895622 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899285 | GAGGCTTAGGCAGGC[A/G]GATTGCTTGAGCCCA | 11060 |
rs750907017 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936616 | GTGATGGCGCGAGCT[A/G]GGGGAACCAAAGCCG | 11060 |
rs750911437 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835804 | TAAAACCAAAGTAAA[-/T]TTTTTTTTTTTTTTT | 11060 |
rs750918538 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783135 | TCTGCCTCAGCCTCC[A/G]GATACCTGGGATTAC | 11060 |
rs750921911 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782806 | GTCAACATCATTGTC[A/G]CTTAGCCATAGCTAC | 11060 |
rs750928501 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784575 | GAAAAGAAAAAGCCA[G/T]GTTCGCCTGAGAATG | 11060 |
rs750931879 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824240 | TGCAGTGTTTAATTT[C/T]CCCTCTTCCTTCAGA | 11060 |
rs750941834 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860991 | ATGCCAGTAGCGAGA[A/C]AGTGAAGAGGCTTTT | 11060 |
rs750969912 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826181 | CTGAGTCAGGAGAAT[C/T]GCTTGGACTGAGGAG | 11060 |
rs750975606 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780907 | GTGGCAAATGCCTGT[A/C]GTCCCAGCTACTCAG | 11060 |
rs750993298 | snp | A/C | 1.65581e-05 | 0.00287728 | intron-variant | WWP2 | GRCh38.p7 | 16:69888011 | TCATTCTTAGTTGAT[A/C]TTTAAAGTATGATTT | 11060 |
rs751002274 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812803 | CAGCTTGTTTATTAT[C/T]GATGACATTAACTTT | 11060 |
rs751010011 | snp | A/G | 1.78058e-05 | 0.00298372 | missense | WWP2 | GRCh38.p7 | 16:69871913 | AACTCAGGCCACAGT[A/G]GCTTGGCCAATGGCA | 11060 |
rs751012894 | snp | A/G | 3.48123e-05 | 0.00417192 | missense | WWP2 | GRCh38.p7 | 16:69939039 | CAGGTGGTGAAGGAG[A/G]TGGACAACGAGAAGA | 11060 |
rs751024342 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771535 | TATAGGCATGAGGCA[C/G]AGAGCCTGAAGGACT | 11060 |
rs751068536 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908034 | TCGCTTGAGCTCAGG[A/G]GTTCCAGACCAGCCT | 11060 |
rs751077833 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843772 | TACTTGGGAGGCTGA[A/G]GTGGGAGGATTGCTT | 11060 |
rs751089239 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813599 | TCCAGAGTAGCTGGG[A/G]CTACAGGTGTGTGCT | 11060 |
rs751090271 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833354 | AGTGTGGGTCTGTGT[A/G]TCTCTCTGTCCCTCA | 11060 |
rs751094487 | snp | A/G | 4.95135e-05 | 0.00497537 | missense | WWP2 | GRCh38.p7 | 16:69798709 | AGCCCAAGGTGCATA[A/G]TCGTCAACCTCGAAT | 11060 |
rs751130699 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856531 | CCTGTAATCCCAGCA[C/G]TGTGGGAGACTGAGG | 11060 |
rs751150909 | snp | A/C | 1.66056e-05 | 0.00288141 | intron-variant | WWP2 | GRCh38.p7 | 16:69887997 | TATAAATAAAATTCT[A/C]ATTCTTAGTTGATCT | 11060 |
rs751158323 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920275 | TGCTCCAGGGTCGAC[A/G]ATCATGCCCCTCTCC | 11060 |
rs751174424 | snp | C/T | 1.66615e-05 | 0.00288626 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931882 | CCTGGACTATGGGGG[C/T]ATCGCCAGGTGAGCT | 11060 |
rs751180681 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856155 | TAAAAAGTAACTTAA[C/G]AACGTGAATGACTCT | 11060 |
rs751209257 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821726 | CTTTTCTTTCTTACT[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs751215399 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877578 | ATTCGCAACTTGGCT[A/G]ACTGTCACAAGAGTC | 11060 |
rs751222503 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844321 | TAGAACAGCGGTGGG[C/T]GAGGAATACTTGAGC | 11060 |
rs751241119 | snp | A/G | 1.64931e-05 | 0.00287163 | missense | WWP2 | GRCh38.p7 | 16:69798784 | CCAAGAAGACTGGGA[A/G]GCGCATTGGGAGCTC | 11060 |
rs751248420 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831045 | ATGGGCCTATGGGAT[C/T]GAGGGCAGAGGGAGG | 11060 |
rs751271043 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802579 | TCATGTTGTAACATG[C/T]GTCAGAAGATTTTTC | 11060 |
rs751293455 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792368 | CTTCTTAAGAGCTTT[C/T]TCAGTGTATAATTTT | 11060 |
rs751312260 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904049 | AGATGTTATAAAAGA[C/G]AGGCTTGCTGCCATT | 11060 |
rs751335329 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861852 | AACTGGCCCAGCTCC[A/G]CTGAATTTTTTTTTC | 11060 |
rs751344336 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832601 | GTCCGGAGTGCAGTG[A/G]CATGGATCTCAGCTC | 11060 |
rs751345623 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921910 | GAAACCCTGTCTCTA[A/C]TAAAAATACAAAAAT | 11060 |
rs751355850 | snp | C/T | 1.78204e-05 | 0.00298494 | missense | WWP2 | GRCh38.p7 | 16:69939848 | CTCAATAGCTTCAAC[C/T]GTCTGGATCTTCCAC | 11060 |
rs751371855 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779099 | GGATTACAGGTGCCC[A/G]CCACCACACCCGGCT | 11060 |
rs751421548 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810996 | CTGACCTCAAGTGAT[C/T]TGCCCGCCTTGGCCT | 11060 |
rs751425601 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808441 | AGTTTCACTCTTGTC[A/G]CCCAGGCTGGGGTGC | 11060 |
rs751428536 | snp | G/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909943 | CCTCTGACTGTTTTT[G/T]TAAATAAGGTTTTAT | 11060 |
rs751473066 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879523 | TGTGGCATTTTTGAT[G/T]CATCCATGTTGTAGC | 11060 |
rs751500324 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851735 | CCTGTAATCCTAGCA[C/T]TGTGGGAGGCCGAGG | 11060 |
rs751505730 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766614 | TGGTCCCAAAACCTG[C/T]CAGTGGTACTCCTTA | 11060 |
rs751515381 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796709 | GCCTCAGTTAACCTT[A/G]GTCCGTGTGTAAATC | 11060 |
rs751516740 | in-del | -/T | 1.6599e-05 | 0.00288084 | intron-variant | WWP2 | GRCh38.p7 | 16:69798845 | GTAAGAGAAAGCCCC[-/T]TCTTTTTGAACGCAG | 11060 |
rs751546339 | snp | A/G | 1.67363e-05 | 0.00289272 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933078 | GTGTGGCCGCGCCCT[A/G]TGTGTGTCTCTCTCT | 11060 |
rs751563099 | snp | C/T | 1.92676e-05 | 0.00310378 | missense | WWP2 | GRCh38.p7 | 16:69842039 | GATCACAGCTGCCTT[C/T]GAGAGACTCCAGTGG | 11060 |
rs751563211 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888555 | GAATCATTGGAGGAT[A/G]TTCGCCTAGATCCTG | 11060 |
rs751586629 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | WWP2 | GRCh38.p7 | 16:69840083 | ATCTTAACTTGGGGT[A/G]CATTCTCTTTAGCCC | 11060 |
rs751600274 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767820 | CATTATGGACTCTGA[A/C]ATTTCTTTTCTTTCT | 11060 |
rs751603209 | snp | C/G | | | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925475 | CTGGGCCCCCTCCCT[C/G]CTGGCTGGGGTAAGT | 11060 |
rs751612967 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935615 | CCGCACCAGCTGGCT[C/G]TGCCCAGTCCTTGCG | 11060 |
rs751617865 | snp | G/T | 3.32165e-05 | 0.00407519 | intron-variant | WWP2 | GRCh38.p7 | 16:69786969 | TATCAGATATTCTCT[G/T]AATTCTTTTTTCTGT | 11060 |
rs751625277 | multinucleotide-polymorphism | AC/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872278 | CTGGAGTGCAGTGGC[AC/GT]GATCTCGGCTCACTG | 11060 |
rs751634416 | snp | A/C | 1.65266e-05 | 0.00287455 | stop-gained | WWP2 | GRCh38.p7 | 16:69937217 | GGAGTGGCTGCGCTA[A/C]TTTGACGAGAAAGAG | 11060 |
rs751646186 | snp | C/T | 9.91719e-05 | 0.00704103 | intron-variant | WWP2 | GRCh38.p7 | 16:69930119 | TCACCCTTTTCTTCC[C/T]GTGTTTCCAGGATGA | 11060 |
rs751646868 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896923 | ATACAGATACACGTA[C/T]AACACACATCTACCA | 11060 |
rs751657715 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887916 | AAAACTTTTTGCTGT[C/T]GCCCAATACATGTAG | 11060 |
rs751668879 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797589 | ATCTTTATTTATTTC[A/C]GTTAAAATTTATAAA | 11060 |
rs751676355 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841110 | TTCTGGTATGCACTA[A/G]GTCTTAGACCAGGCC | 11060 |
rs751688419 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768649 | ATAACAAGTACCAAG[A/T]CATGGCAGTCCTGAC | 11060 |
rs751697149 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828292 | TGCCTTCCCAGGAAC[C/G]CTTCTTGATCTTCCT | 11060 |
rs751715302 | snp | C/T | 1.64923e-05 | 0.00287156 | missense | WWP2 | GRCh38.p7 | 16:69888195 | AGGAACCCAGCACTT[C/T]GGGTACACAGCAGCT | 11060 |
rs751720088 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907144 | TTACTGTGAACTGGT[A/G]CATGGAGGGCTATCT | 11060 |
rs751720627 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829176 | AAGTCTGCCCACTTC[C/T]TCAGCTCCACTTCTG | 11060 |
rs751726517 | in-del | -/CT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808835 | ACGCTGACATAAACA[-/CT]CTCAGGACATGTATT | 11060 |
rs751736850 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906417 | GGGGCTGATCAATGC[A/G]GTCCACTAACCAGAC | 11060 |
rs751754943 | snp | A/G | 7.40371e-05 | 0.00608383 | intron-variant | WWP2 | GRCh38.p7 | 16:69888269 | GTAGTCTTCTGTCCC[A/G]TAACAGATCTCTCCT | 11060 |
rs751755190 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883072 | GCAGGAGGATCGCTT[A/G]AACCCAGGAGGTGGA | 11060 |
rs751759957 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903501 | TGGCCGGGCGCAGTG[G/T]CTCACACCTGCAATC | 11060 |
rs751797314 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814884 | AGATAAATAAAACTA[C/T]TGAACCTTGGAACTT | 11060 |
rs751799849 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860547 | TGGCCACCTGGGTGG[-/A]AAGTCCAGGAAGAGA | 11060 |
rs751808613 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933873 | GGACACGTGTCCCCA[C/T]ACTAACCTGAGACAC | 11060 |
rs751832527 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829676 | AAGCATCTGGCTGCT[A/C]AGGGGACCATATGTT | 11060 |
rs751874497 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917417 | TGGCTGTGGCTGGCT[C/T]AACATACATCACATG | 11060 |
rs751913709 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776023 | AATAGAGTGTATGCC[G/T]TTCAGCCCTAATTCC | 11060 |
rs751914087 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931208 | GGTGGAAGTATCACC[A/G]GTTCCGTTTCCTCTG | 11060 |
rs751964806 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929870 | AAGCTGTGCTGGGGC[A/G]CAGGGTGCCTCAGGA | 11060 |
rs751973193 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817894 | AGCCATTGTGCCCAG[C/G]CTAAATTCTTGTAAA | 11060 |
rs751992065 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803780 | GGGCACAGTGGCGCA[C/T]GCCTGTAATCCCAGC | 11060 |
rs751998645 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907235 | ACTGAGGAGGTTGCT[-/AG]ATGCCTGTGGGTTTT | 11060 |
rs752003822 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848138 | GGGATTAACATAAGG[G/T]ATCTTAGTTAAGAAG | 11060 |
rs752018585 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875604 | TTCTAAATCCTTGTT[G/T]TCATTTCAACAGTGT | 11060 |
rs752046138 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765239 | AAAAAGTTTCACCTT[A/T]TTGTCTTTTTTTTTC | 11060 |
rs752053773 | snp | A/G | 4.43262e-05 | 0.00470756 | intron-variant | WWP2 | GRCh38.p7 | 16:69917928 | GGGCCGCCTCCCTGC[A/G]CTTGCGAATGTGCAG | 11060 |
rs752061146 | snp | G/T | 1.77128e-05 | 0.00297591 | intron-variant | WWP2 | GRCh38.p7 | 16:69935806 | GAGCTGGTCTTGGCA[G/T]TGCCCAGGGAAGGCC | 11060 |
rs752077925 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804814 | TCCCCACATAGGAAC[A/G]TGGAATGTTTCTAAA | 11060 |
rs752079959 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793673 | AGTAGATTGCCAGAA[A/G]GAAAAAATCTCAAAA | 11060 |
rs752097582 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835585 | TCTTGTTAACATTTT[C/T]TTGCCAAATTTGTTT | 11060 |
rs752100569 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786641 | TTTTTAGTAGAGACG[A/G]GGTTTTGCCATGTTG | 11060 |
rs752106625 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813469 | GCCCAGCCTTTTTTT[-/T]GTTGTTTTTTAAATT | 11060 |
rs752113529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865330 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC | 11060 |
rs752125261 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902231 | CATGAGAGAGATGCT[G/T]ATGTCATTCTAATAA | 11060 |
rs752127869 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877377 | ATAGAATTGAAGAGG[G/T]TTCGGGTCTTGCTCC | 11060 |
rs752142747 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822927 | GGATCATTTGAGGCC[A/G]GGAATTCAAGACCAG | 11060 |
rs752150293 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782925 | ATCCTCTTGCCGCAG[C/T]CTCCCAGTGTGCTGG | 11060 |
rs752169608 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818374 | ACCACGCCCAGCTAA[-/T]TTTTTTATTTTTAGT | 11060 |
rs752169838 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794735 | GTGGAAGTCTTTAAA[A/C]ATCATTGTTGCCTTG | 11060 |
rs752208286 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793364 | TAAAAAAATAATAAT[-/A]AATAAATAAATAAAT | 11060 |
rs752217029 | snp | G/T | 0.000666422 | 0.0182419 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931778 | GGGAGAGTGGCAGGC[G/T]GGCCCGATGCTCTGT | 11060 |
rs752219825 | snp | A/G | 1.67315e-05 | 0.00289231 | missense | WWP2 | GRCh38.p7 | 16:69871835 | GGTGCTTCAGCCAGA[A/G]CAACCCCAGCAACCG | 11060 |
rs752230894 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823938 | GCCTGTGCTGTTTCT[C/T]ATCAGCCGTGTAGCA | 11060 |
rs752235976 | snp | C/G | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933442 | CATGAGGTTTCTCAT[C/G]TGAAGGCAGCATGGA | 11060 |
rs752247326 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805164 | CGTGCCTCAGACTAC[C/T]GAGTAGCTGGGATTA | 11060 |
rs752305166 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909103 | GTTGATGCATTCCGC[C/T]GTACCCTATGCCCAG | 11060 |
rs752309163 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837475 | TAGATAAACCAGATA[G/T]AAGAGCTAACTTGGA | 11060 |
rs752320752 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803367 | TTGGAACATTTACAT[-/A]AAAAAAAACATTATC | 11060 |
rs752322418 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876382 | TTCGTTTTTTGTTTT[C/T]GAGATGCAGTCTCAC | 11060 |
rs752324705 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780934 | TCAGGAATCTGAGGC[A/G]GAAGGATCACTGGAA | 11060 |
rs752326277 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925464 | ACCATGATCCCCTGG[A/G]CCCCCTCCCTCCTGG | 11060 |
rs752344677 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783925 | TGCCACTGCACTCCC[A/G]GCATGGGCGACAGAG | 11060 |
rs752353935 | in-del | -/AAAT | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761124 | CTCAAGCAAGCAAAT[-/AAAT]AAATAAATAAATAAA | 11060 |
rs752367875 | snp | C/G/T | 4.95293e-05 | 0.00497621 | missense | WWP2 | GRCh38.p7 | 16:69787027 | TGGCATCTGCCAGCT[C/G/T]TAGCCGGGCAGGAGT | 11060 |
rs752376497 | in-del | -/AAAAA | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932331 | GCGAAACTCCATCTC[-/AAAAA]CAAAACAAACAAAAA | 11060 |
rs752380944 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920327 | CCCAGTGCGCTCTGC[A/G]CACTTTCTTGGGCTA | 11060 |
rs752389981 | snp | C/T | 1.9856e-05 | 0.00315081 | intron-variant | WWP2 | GRCh38.p7 | 16:69939831 | TGTCGTGCTTCCCCA[C/T]TCTCAATAGCTTCAA | 11060 |
rs752395142 | snp | C/T | 3.2963e-05 | 0.00405961 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936390 | CAAGGTGACGACCCA[C/T]GAGCTGAAGGAGGGC | 11060 |
rs752397965 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855267 | ACTTATTGAAAATAT[A/G]GTGGAGGTATTTGTC | 11060 |
rs752410088 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895975 | AGGTCACATGGAATA[A/G]TGTGTGTTTCTGGCT | 11060 |
rs752415269 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835802 | ATATAAAACCAAAGT[-/A]AATTTTTTTTTTTTT | 11060 |
rs752416248 | snp | A/G | 3.46159e-05 | 0.00416014 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871903 | GCCCGTCAAGAACTC[A/G]GGCCACAGTGGCTTG | 11060 |
rs752421129 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773133 | TTCCTTAGCAACAGT[A/C]CTGACGGGGAGCTCC | 11060 |
rs752444568 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800752 | GTATTTTTAGTAGAC[A/G]TGAGGTTTCACTGTG | 11060 |
rs752449815 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895067 | TCGGATTTGCCATCT[C/T]CTCTACCCCCCTGCC | 11060 |
rs752466834 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932222 | TAATCCCAGCTCCTG[G/T]GGAGGCTGAGGCGGG | 11060 |
rs752472899 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830936 | CTTCTGGAATTTCCC[A/C]CGGTTCCCTTCCTCT | 11060 |
rs752475646 | in-del | -/G | 1.64762e-05 | 0.00287016 | intron-variant | WWP2 | GRCh38.p7 | 16:69840115 | TCCATGTTGCCTTTT[-/G]TACCCCACAGTGGAG | 11060 |
rs752479198 | in-del | -/G | 6.65264e-05 | 0.00576704 | intron-variant | WWP2 | GRCh38.p7 | 16:69929549 | GGACTTGGGCTGAGA[-/G]GGGGGCCGGGCTGGG | 11060 |
rs752520735 | in-del | -/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876354 | GGCATGTTTTTTGGG[-/GT]TTTTTTTTTTTTTCG | 11060 |
rs752534568 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791389 | CCTGCCACCACACCC[A/G]GCTAATTTTCGTATT | 11060 |
rs752556716 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792557 | AAAATATCACCCTGC[A/T]GATTAACTGTAGGTT | 11060 |
rs752560262 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901329 | ATACTTGAGTACTTC[C/T]AGTGTATTCTTCTTA | 11060 |
rs752566957 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819112 | CTGCATTGCCTTTAG[A/G]ATATATTCTGGGATC | 11060 |
rs752590456 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869672 | TTTTTTCCTTACTCA[C/G]AAGTATACAAGCTCA | 11060 |
rs752617628 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869505 | CACGCCACCACACCT[A/G]GCTAATTTTTTAAAT | 11060 |
rs752619899 | snp | A/T | 1.64868e-05 | 0.00287109 | intron-variant | WWP2 | GRCh38.p7 | 16:69908747 | CTCATGCTACCCTTG[A/T]CTTTATTTTTCAGAT | 11060 |
rs752641472 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871386 | ATCATCTTTCTAGCT[A/G]TAGAGAAAATTGCTT | 11060 |
rs752641599 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861393 | AGTCTAATGAAATTG[C/T]CACCTTTGAGAAGGT | 11060 |
rs752666612 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832282 | CAGTTCAGTAGCCAT[C/T]TATGACGGGCCATTC | 11060 |
rs752688147 | snp | A/G | 6.34176e-05 | 0.0056307 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933191 | GCACCCTCTGCGTCG[A/G]CGGACTCCTCGTCTG | 11060 |
rs752692122 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848042 | AAATTTCCATAGTCA[C/T]ACAGGGAAATGGAAC | 11060 |
rs752721464 | snp | C/G | 3.37262e-05 | 0.00410633 | intron-variant | WWP2 | GRCh38.p7 | 16:69937106 | CCACCCATGGCTGCT[C/G]TTTGGTCTCAGGCTG | 11060 |
rs752751843 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819894 | AGCCCCTGGCAACCA[C/T]GAATCTACTTTGTGT | 11060 |
rs752756646 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765852 | TGGGGAGTTGGGGGC[A/G]GGGGTTCTCACTTTT | 11060 |
rs752759351 | snp | C/T | 1.6483e-05 | 0.00287076 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939965 | CCCCTCCCACGCCCC[C/T]CAGCGCACATGTAGT | 11060 |
rs752781641 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931187 | GTGCTTATGACCGCA[A/G]TTTTCGGTGGAAGTA | 11060 |
rs752795058 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918595 | TTTGCTGAAAAAGTT[G/T]GTTATCTTTGGTCTA | 11060 |
rs752795485 | snp | A/T | 1.98876e-05 | 0.00315332 | missense | WWP2 | GRCh38.p7 | 16:69842116 | TGCTTTGGTGGAAGA[A/T]CCCGGTAAGACCCCC | 11060 |
rs752811846 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766374 | TTCACTTTCTCCACA[C/T]AGGACCCAGGGCAAG | 11060 |
rs752834019 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898844 | GAGTAGCTGGGATTA[C/G]AGGCATGTGCCACCA | 11060 |
rs752856376 | snp | C/T | 1.658e-05 | 0.00287919 | intron-variant | WWP2 | GRCh38.p7 | 16:69929538 | CCCAGGGGTAAGGAC[C/T]TGGGCTGAGAGGGGG | 11060 |
rs752857573 | snp | A/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839952 | TACAACAGTGATTTC[A/T]TTAGACATATTCCTT | 11060 |
rs752865239 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926699 | ATTTGTTGATGTTCA[C/G]CTTGGGGATCCCTTA | 11060 |
rs752869572 | snp | C/G/T | 3.30848e-05 | 0.00406712 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935891 | CGACACGGGCTTCAC[C/G/T]CTCCCTTTCTACAAG | 11060 |
rs752869922 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838803 | AAATAGCAGCAGACT[C/T]ACTCAGAAAAGAATT | 11060 |
rs752884453 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842453 | GAACATAGTACCTGA[C/T]TGGTAGTTTTTCAAT | 11060 |
rs752888876 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796544 | CATATGACTATTCTG[C/T]GAAAAGACCAAAATT | 11060 |
rs752896102 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874504 | ATTTGAGGCCAAACC[A/G]GAGCTGGGTTCCAGG | 11060 |
rs752901791 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767723 | TGTTTGTGATTAATC[A/G]TTTCTCAGAACGACT | 11060 |
rs752920735 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785811 | TGTTGTTTTTTAGTA[G/T]AGATGGGGTTTCATC | 11060 |
rs752946433 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888121 | TGCTGCACCCTTGAG[C/T]GTGACCCCGAATCCC | 11060 |
rs752956957 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935665 | AGTCCCTCTGTAGGT[A/G]CAAGTCAGGATAAAG | 11060 |
rs752958878 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848926 | AGAGCCTCTTAGATA[-/G]TTTTCTTTCTCACTC | 11060 |
rs752965803 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879657 | CTCCACCTTTTGGCT[A/G]TTGGAATAATGCGGG | 11060 |
rs752967912 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856973 | TAGAGTTTTAAAAAA[A/C]CATATGATTTTAAAC | 11060 |
rs752977876 | snp | C/G/T | 6.80068e-05 | 0.0058309 | intron-variant | WWP2 | GRCh38.p7 | 16:69799152 | CTGCTTGGATGTAAT[C/G/T]AATCAGGTATTTGTT | 11060 |
rs752987931 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877686 | TGAGAGACATATGAC[C/T]CTTCCTTTTGCTTGA | 11060 |
rs753038154 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | WWP2 | GRCh38.p7 | 16:69888185 | GCTGAAGGAGAGGAA[C/T]CCAGCACTTCGGGTA | 11060 |
rs753044595 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898437 | TCACCTAACCAATTC[A/G]TACTCCTGTGAGCAT | 11060 |
rs753062895 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787520 | GCTTGAGCCTGGGAG[C/T]TCAAGGCTGCAGTGA | 11060 |
rs753063546 | in-del | -/CAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807955 | AGCAAAACCCTATCT[-/CAAA]CAAACAAACAAAACA | 11060 |
rs753089939 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884088 | CTGTTGTGTTTCTTG[C/T]GGTTCTTTCAAAGAT | 11060 |
rs753107645 | snp | A/T | 4.92429e-05 | 0.00496176 | intron-variant | WWP2 | GRCh38.p7 | 16:69939008 | TTGCCTGACTGTGCC[A/T]TGACTTGCGGACTTC | 11060 |
rs753126119 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801840 | ATGTTTATGACATCA[A/G]TGAAACTAAATTGAG | 11060 |
rs753139309 | snp | A/G | 1.67699e-05 | 0.00289563 | intron-variant | WWP2 | GRCh38.p7 | 16:69937657 | GGTTCTGGCAGGTGG[A/G]TCCCGGGCCCAGGCC | 11060 |
rs753144100 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918521 | GGTAGAGTTAAGTAT[C/G]ACAATAAAGACTGTA | 11060 |
rs753145112 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814754 | CCTTATTGCTCCGTG[A/C]GGATGGAGTGTTCTG | 11060 |
rs753160344 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858440 | CTTCTGGGTGGGTCA[C/T]GTTGCTGGTTTACGT | 11060 |
rs753199202 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774445 | TGGTTTTTGTTGAGA[C/T]GAGGTTTTGCCCTAT | 11060 |
rs753199713 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917611 | GCAACCTCTGTGACA[C/G]GGCCTGCCCGGCTGT | 11060 |
rs753203946 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845974 | AGAATTGCCTGAACC[C/T]GGGAGGCGGAGGTTG | 11060 |
rs753225945 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802965 | AATCTGAAATCCAAA[A/G]CACTTCCAGTCCCAA | 11060 |
rs753231567 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929943 | GGTTTTTGGCCATGA[A/G]ATAATAAGTGACCTC | 11060 |
rs753232017 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930805 | TAAGACCAGGAATTC[A/G]AGGCCGCAGTGAGCC | 11060 |
rs753243617 | snp | C/T | 1.648e-05 | 0.0028705 | missense | WWP2 | GRCh38.p7 | 16:69936368 | TCCAGGACATGGAGA[C/T]ACTGGGCAAGGTGAC | 11060 |
rs753283106 | snp | A/G | 3.30316e-05 | 0.00406383 | missense | WWP2 | GRCh38.p7 | 16:69917828 | AGCAGTGGCAGTCGC[A/G]GCGGAATCAGCTCCA | 11060 |
rs753284803 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763539 | TTCCTAATGTATTAT[G/T]AGTTCAAGTTTTTGG | 11060 |
rs753295562 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834042 | GTGACCTCCTACCTG[G/T]TCTTGTGTACCTCAG | 11060 |
rs753297316 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761910 | AAAAATACTTTTTTT[A/G]GTATAAATATGTCCC | 11060 |
rs753302747 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793433 | ATTGACACAAAACAG[G/T]CCATATGGGAGACAG | 11060 |
rs753320975 | in-del | -/CACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912372 | AGGGAGTTAGATTCA[-/CACACA]CACACACACACACAC | 11060 |
rs753327675 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821847 | ATAGGCGTGAGCCAC[A/C]ATGCCCGGCTATTTT | 11060 |
rs753346422 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931493 | ATTTAAAGTTCTTTT[C/T]TTTTTTTTTTTTCAG | 11060 |
rs753386199 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835302 | TCCAGCCACACTTAC[A/G]CCTTTCAGCCTCCCC | 11060 |
rs753426948 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | WWP2 | GRCh38.p7 | 16:69917825 | ATGAGCAGTGGCAGT[C/T]GCAGCGGAATCAGCT | 11060 |
rs753431611 | in-del | -/ACAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826722 | CTCTCTAATAAAAAT[-/ACAA]AAAAAAAAAAAAAAA | 11060 |
rs753434083 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | WWP2 | GRCh38.p7 | 16:69936281 | CCCTGACACGGTAGA[C/T]ATCTCCCCACTTGGT | 11060 |
rs753444063 | snp | C/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839779 | CAGGGGGATATTACT[C/T]GCAACTAATTTCTTC | 11060 |
rs753462718 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891004 | GGGTGTCGGAGACCC[A/G]ATTTTCCAACCCAGA | 11060 |
rs753465368 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795630 | ATTTTTCTATAGATT[A/G]GAAACTTAAAAATAG | 11060 |
rs753465393 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817575 | TTTTTGTTTTGTATA[A/G]ATGTACCCACAGTTT | 11060 |
rs753472180 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784172 | TGGCATGATCTCGGC[A/G]CACTGCAACCTCTGA | 11060 |
rs753509815 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937731 | GAGGAGGCCTCACGC[A/G]CAAGGACCTTCAGCT | 11060 |
rs753513030 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877421 | GCTTAAGAGAATGTC[C/G]AGGCTGGTTTGATCT | 11060 |
rs753514168 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822605 | GGCTTCCTGGAGGAA[A/G]TGACACCTGGACACC | 11060 |
rs753514813 | snp | A/T | 2.1397e-05 | 0.00327079 | intron-variant | WWP2 | GRCh38.p7 | 16:69842133 | CCGGTAAGACCCCCC[A/T]TGGTGAGGACAAAGA | 11060 |
rs753519439 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909169 | GGGCTTCGTGAGAAT[A/G]CCGCCAAGTTATCCA | 11060 |
rs753530267 | in-del | -/ATAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778073 | GAAACCCTGTCTCAA[-/ATAT]ATATATATATATATA | 11060 |
rs753533462 | in-del | -/ACCTACCT | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761606 | ATCATCTATCTATCC[-/ACCTACCT]ACCTACCTACCTACC | 11060 |
rs753539468 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782400 | GCAGGAGCCAACCAA[C/G]AAGGCTCAGGTGGGG | 11060 |
rs753549368 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865222 | AACTAGCAAATTTTT[A/G]TTATTTTTGTAGAGA | 11060 |
rs753551231 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815383 | CTCGAGCATAGCTCA[C/T]TGTAACCTTGAACTC | 11060 |
rs753554127 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887714 | CCTGGCCCCAACACA[C/T]TCCTGTTATGTTGAT | 11060 |
rs753570705 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923804 | ACGTGTGTTTTCTCA[C/T]TTGTTCCTTTGCCTC | 11060 |
rs753579058 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894075 | TTTCAGGTTGCTGCA[-/T]TTTTTTTTTTTTTTA | 11060 |
rs753593445 | snp | C/T | 1.74848e-05 | 0.0029567 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933180 | AGGATACCGGGGCAC[C/T]CTCTGCGTCGACGGA | 11060 |
rs753600026 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811999 | TTCCCGTTTTTGCAG[G/T]GTTGTTAATCTAATT | 11060 |
rs753604834 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810893 | CTGAGCAGGTGGGAT[C/T]ACAGGTTCACACCAC | 11060 |
rs753615939 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769943 | GCAATGGCATAATCT[C/T]GGCTCGCTGCAGCCT | 11060 |
rs753663554 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922162 | ATTATCGAGAAACAG[A/G]CAACTTGTTTCTTAC | 11060 |
rs753688057 | snp | A/G | 3.39104e-05 | 0.00411753 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933051 | CTCCAGGCTCTGCTT[A/G]GTGGGCTTCTGGTGT | 11060 |
rs753709587 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798946 | CTTTTTCTACCTATG[A/G]TACCCAAGGTGACTC | 11060 |
rs753723242 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789743 | ATGTTGTCAGACTTT[-/A]TAACTTTTGCCTGTT | 11060 |
rs753749769 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932775 | AGTCCAAAGCATTGT[C/T]TTGCCTTCACCCTGG | 11060 |
rs753772982 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69930149 | ATCCAGGAACCAGCT[C/T]TGCCCCCAGGATGGG | 11060 |
rs753776280 | snp | C/G/T | 0.00271002 | 0.0367133 | missense | WWP2 | GRCh38.p7 | 16:69937212 | CCGCTGGAGTGGCTG[C/G/T]GCTACTTTGACGAGA | 11060 |
rs753799970 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789402 | GCCTGGCTACTTTTT[A/G]TATATTTAGTAGAGA | 11060 |
rs753800039 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799759 | TAGTATTACAAATAG[C/T]GCCCTGTGCTTACTC | 11060 |
rs753800372 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797676 | GGCAGATCATCTGAG[C/G]TCAGGAGTTTGAGAC | 11060 |
rs753819563 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895277 | ACTTCAGCACTAGCC[A/G]AAGAGTCTTACCCAA | 11060 |
rs753833122 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905944 | CACCTTAAAGGATGA[A/G]GGCAAGGATTGCATA | 11060 |
rs753840545 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869590 | AGCTCAAGTGCCGTC[C/T]CATCTCAGCCTCCCA | 11060 |
rs753853941 | snp | C/T | 1.69556e-05 | 0.00291162 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939877 | ACCCTACAAGAGCTA[C/T]GAACAGCTGAGAGAG | 11060 |
rs753914076 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847692 | GGATTACAGCTGTGA[G/T]CCACCGCGCCTGGCC | 11060 |
rs753917725 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860387 | GAGGTTCACAAAACA[A/G]GACATGATCTCTGCC | 11060 |
rs753918144 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861353 | CACCATTTACTATAC[C/G]TTCTCTCTCAAGGTG | 11060 |
rs753935125 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | WWP2 | GRCh38.p7 | 16:69930266 | GAGTCGGGGTAAGGA[C/T]TTTGTGCAGGTAGCA | 11060 |
rs753949206 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918929 | GCTCACTGCAACCTC[C/T]GTCTCCTAGGTTCAA | 11060 |
rs753950572 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819031 | CAGTGACAATTCTGT[C/G]TCACTCAGGCTAAAA | 11060 |
rs753952196 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805491 | ACTTCTAGGTGTAAG[C/G]CTGGGTATTAGTAAC | 11060 |
rs753958992 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777212 | ACATATGGAGATATC[A/G]TATATGCACCTATTA | 11060 |
rs753982043 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789752 | AGACTTTTAACTTTT[A/G]CCTGTTTCATTGGTG | 11060 |
rs753992692 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927353 | CCCCAGGAGAGACCC[C/T]GCATCTTCCCCACAC | 11060 |
rs754002727 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849130 | CCTATCCCAGAAAGG[A/G]AAGAAAAATAAACTC | 11060 |
rs754009689 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915152 | GAGAATCTGGGGATG[C/T]ATCAGTGATAGGTTC | 11060 |
rs754011116 | snp | C/T | 4.97401e-05 | 0.00498674 | intron-variant | WWP2 | GRCh38.p7 | 16:69938987 | CAAAGTACTGGGCCC[C/T]GTGGGTTGCCTGACT | 11060 |
rs754025922 | snp | G/T | 1.6546e-05 | 0.00287624 | intron-variant | WWP2 | GRCh38.p7 | 16:69934162 | GTCTGCCTAGTTCCC[G/T]CCTCCTCTCCCTCCT | 11060 |
rs754034157 | snp | G/T | 2.58903e-05 | 0.00359784 | intron-variant | WWP2 | GRCh38.p7 | 16:69842004 | GCTTCTGTCTTTTCT[G/T]GTGATTGATTCCTTT | 11060 |
rs754042105 | snp | C/T | 1.67525e-05 | 0.00289413 | intron-variant | WWP2 | GRCh38.p7 | 16:69929438 | TTCTTTCTTTCTTCT[C/T]ATGTGGCAGAGAAGA | 11060 |
rs754049537 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765058 | AAAATACAAAAATTA[A/G]CCAGGTGCAGTGGCG | 11060 |
rs754056242 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766318 | CCCTGGATGATGGCA[A/G]CAGCCTCCTAACTTG | 11060 |
rs754062925 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789081 | ATTATATTTTGCGAC[-/AG]AGTCTCGCTCTGTCG | 11060 |
rs754080571 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936545 | ACCTGTGGCCCATCG[A/G]TCACTGTGGATGCCA | 11060 |
rs754080934 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805159 | ATTCTCGTGCCTCAG[A/C]CTACTGAGTAGCTGG | 11060 |
rs754107974 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837368 | ACTGCACCCAGCCCA[C/T]TGGCTCTTTTTGAAG | 11060 |
rs754115987 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934078 | CCCCGCCTCCTCCAT[C/T]AACCCGGACCACCTC | 11060 |
rs754154093 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798187 | GGCAGTTTTAAGAAC[-/T]TTTAAAAAGTGTTCG | 11060 |
rs754163804 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926781 | TCTCAGAGATTGGCA[C/G]CAACTCCAATGCGAG | 11060 |
rs754178456 | in-del | -/TT/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793911 | TGTTATTATCCTTGC[-/TT/TTT]TTTTTTTTTTTTTTT | 11060 |
rs754182260 | snp | C/T | 1.65501e-05 | 0.00287659 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937616 | CATCTACCGGCACTA[C/T]ACCAAGAACAGCAAG | 11060 |
rs754232226 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795261 | AAAAAATGCGGATAC[-/AC]ACACACACACACACA | 11060 |
rs754247670 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796511 | GTTGCGGCTCACTGC[C/T]GCTGCCCAGTAGTAC | 11060 |
rs754249748 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935716 | CCTCCCGCTGCGTCC[A/G]AGGCAGCTGCTGCTG | 11060 |
rs754277501 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934998 | GGGAGGGGCGTCCCA[A/G]CGTCTGTATTTAACT | 11060 |
rs754293445 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907393 | AATAGCATTGGAACA[A/G]ATTTGCATTTTCAAA | 11060 |
rs754301169 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | WWP2 | GRCh38.p7 | 16:69888104 | GGTGTGACGTCCCCA[C/T]CTGCTGCACCCTTGA | 11060 |
rs754311459 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931556 | CGTTTCCAGGCAGAC[A/G]CTTTTCGAAGATTCC | 11060 |
rs754383532 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828008 | GAGACTCCTTCTGGG[A/G]TACCTTGTTACGTGG | 11060 |
rs754399491 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780429 | ATTACAAATACTGCT[A/G]TGATGAACATCCTTG | 11060 |
rs754416650 | snp | A/G | 1.7051e-05 | 0.0029198 | intron-variant | WWP2 | GRCh38.p7 | 16:69799144 | GGAATGATCTGCTTG[A/G]ATGTAATGAATCAGG | 11060 |
rs754433678 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801998 | GCAGTGGCGCGATCT[C/T]GGCTCACCACAACCT | 11060 |
rs754434663 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772800 | GAGTCCTCCCTCCTG[C/G]CTCACCACCAGTGAT | 11060 |
rs754439907 | snp | C/T | 3.29679e-05 | 0.00405991 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931558 | TTTCCAGGCAGACGC[C/T]TTTCGAAGATTCCTT | 11060 |
rs754461753 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835341 | CGAATCTGTCACTCA[A/G]TTAGCTAATGGTTTC | 11060 |
rs754462591 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793528 | GGTAGGGGACTAGGG[A/G]ATGGGTGCTGCTTAT | 11060 |
rs754481103 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835680 | TTGCAGATATCATGA[C/T]ACTTTAATCCCCAAA | 11060 |
rs754483597 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875340 | TCTTCACTGGTGGAA[A/G]GTCTCTCCTCGATGT | 11060 |
rs754538502 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778658 | TTACGGTTATTTCTC[C/T]TGAGACAGAGTCTCG | 11060 |
rs754548156 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822710 | TTTGAGGCAGGAACA[A/G]GCTGGTTGCTGTCAA | 11060 |
rs754553196 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908209 | GAGATTGTGTCACTG[A/C]ACTTCAGCCTGGGCA | 11060 |
rs754556163 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781345 | CTTTGGCTTTTACTC[G/T]TTTTTTGTTTTTGTT | 11060 |
rs754569292 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884410 | GGGAGGATCGCTTGA[G/T]CTCAGGAGTTTGAGA | 11060 |
rs754584756 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809554 | GGTGTATCACCTGAG[A/G]TCAGGAGTTCGAGAC | 11060 |
rs754620257 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841674 | TGCCCCCGATTTCTG[G/T]CCCCTACTTTGCATG | 11060 |
rs754639439 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920303 | TCCAGCCAGGGCCCC[A/G]CTGTCTAGCCCAGTG | 11060 |
rs754689712 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799006 | ATAGAGCGTTCATTA[C/T]TATCTAGAGGGTTAC | 11060 |
rs754692336 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797995 | AGTGCTGGGATTCCA[C/G]GCATGAGCCGCCACG | 11060 |
rs754698142 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845127 | CAAAACCTCTCGGAT[A/C]CCCAGTTTTTTTCAG | 11060 |
rs754701403 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894442 | TGGTTACACACGTCT[A/G]CACGTTTTAAGAACT | 11060 |
rs754708117 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829471 | TCTCATTCCAGTCCA[A/G]CCCCGTTCATCTCTG | 11060 |
rs754709887 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769948 | GGCATAATCTCGGCT[C/T]GCTGCAGCCTCTAAG | 11060 |
rs754714923 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854107 | GCTAGTTCTACTTGA[A/T]CCAGATCTGTATCTG | 11060 |
rs754715768 | in-del | -/CAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826723 | TCTCTAATAAAAATA[-/CAA]AAAAAAAAAAAAAAA | 11060 |
rs754729331 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919253 | TCACTGTAACCTCCA[C/T]TGCCCGGGTTCAAGC | 11060 |
rs754755972 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921919 | TCTCTACTAAAAATA[C/G]AAAAATTAGCTGGGC | 11060 |
rs754781773 | in-del | -/CACCA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876109 | ATTATAGGCATGCAC[-/CACCA]CACCCAGCTAATTTT | 11060 |
rs754786989 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842465 | TGATTGGTAGTTTTT[C/T]AATTCTTGCTCCTCT | 11060 |
rs754787189 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893186 | TCTGGGACTCCCTCC[C/T]GGATCCCTGGTGGAC | 11060 |
rs754787651 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904051 | ATGTTATAAAAGAGA[A/G]GCTTGCTGCCATTGG | 11060 |
rs754821051 | snp | C/T | 7.62544e-05 | 0.00617425 | intron-variant | WWP2 | GRCh38.p7 | 16:69939135 | ATCGGTATGTTTTCT[C/T]TCGCCCTCTGGCGTC | 11060 |
rs754831962 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847836 | CCCACTAGGTCTCAC[A/C]TCCCAACTCTGCCAC | 11060 |
rs754845564 | snp | A/C | 1.64895e-05 | 0.00287132 | missense | WWP2 | GRCh38.p7 | 16:69930155 | GAACCAGCTCTGCCC[A/C]CAGGATGGGAGATGA | 11060 |
rs754846385 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868462 | GGCTGGAGTTGATCA[C/T]GGACATGTCTGTCTG | 11060 |
rs754855176 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810306 | CTCTGAGGGGACATT[-/C]CGCCCTGGCCATGGC | 11060 |
rs754863606 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867678 | GTTCTTGAGAGAGGA[C/G]CTTGAGTGAGGACAC | 11060 |
rs754867307 | in-del | -/T | 0.000187073 | 0.00966962 | intron-variant | WWP2 | GRCh38.p7 | 16:69827899 | ATTTCCCCAGGTACC[-/T]TTTAAAAAATTAAAA | 11060 |
rs754875413 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903142 | GGGACAATAATAGTC[C/T]CTGAAAGAGAGACTT | 11060 |
rs754881694 | snp | C/T | 5.91979e-05 | 0.00544017 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933057 | GCTCTGCTTGGTGGG[C/T]TTCTGGTGTGGCCGC | 11060 |
rs754886861 | snp | A/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940069 | GGGACCACACTGTCA[A/T]CTCGCTGCTGGCAGA | 11060 |
rs754899072 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859789 | TCTCTCTGATTTTCT[C/G]TCCTGCCACCTGCTG | 11060 |
rs754914703 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860439 | ATAGCAGTGCCATAA[A/G]GGGAACAATTAGGAT | 11060 |
rs754931807 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911659 | AAATAAAGAGTGCAA[A/T]CGTGCTTCTTAGAAG | 11060 |
rs754934364 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939721 | GAAGGCCTGACTGGC[-/A]GCCCCTGAGCCCTAG | 11060 |
rs754954272 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888566 | GGATGTTCGCCTAGA[C/T]CCTGCCTAGAAAACA | 11060 |
rs754970540 | snp | A/G | 1.69226e-05 | 0.00290878 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931910 | GCTTGAGTGCCCCGG[A/G]AGGCTGCCCTGTACC | 11060 |
rs754989311 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861637 | CTTCTCCTTTTACCC[A/G]CCCTCTCCTTTTTTT | 11060 |
rs755001712 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849149 | AAAAATAAACTCAGG[C/T]GGGTGTGAGTCCACT | 11060 |
rs755020164 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925562 | CTCCCGCGTGTCTTC[A/C]TTCCCTGTTCCTGTC | 11060 |
rs755021459 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805495 | CTAGGTGTAAGGCTG[A/G]GTATTAGTAACCTTT | 11060 |
rs755034377 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765071 | TAGCCAGGTGCAGTG[A/G]CGCCCGCCTGGCTAC | 11060 |
rs755052182 | snp | A/G | 1.6951e-05 | 0.00291122 | missense | WWP2 | GRCh38.p7 | 16:69939878 | CCCTACAAGAGCTAC[A/G]AACAGCTGAGAGAGA | 11060 |
rs755076570 | snp | A/G | 3.30077e-05 | 0.00406236 | intron-variant | WWP2 | GRCh38.p7 | 16:69925522 | GGCCCTTGGCCTTCC[A/G]TCAGCCACGGTGCTC | 11060 |
rs755136848 | snp | A/G | 1.65828e-05 | 0.00287943 | intron-variant | WWP2 | GRCh38.p7 | 16:69930276 | AAGGACTTTGTGCAG[A/G]TAGCAGCAGTGTCAG | 11060 |
rs755147228 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786748 | GAGCGACCATGCCTG[A/G]CAGAGGTGTCTTAGT | 11060 |
rs755174015 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806620 | TCAGCTTCTTTGTTT[C/T]GTCTTGACTCAATTT | 11060 |
rs755182291 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924045 | TAAATCAAGGTGAGC[G/T]TCCCCCACCTCCGTG | 11060 |
rs755186085 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837401 | AAAATGTGTCTCAAG[C/G]TGTTGTATGATGGCT | 11060 |
rs755196485 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766340 | CCTAACTTGTCTCCC[A/T]CTTCCACCCTGGCTG | 11060 |
rs755200869 | snp | A/C/G/T | 6.62829e-05 | 0.00575657 | intron-variant | WWP2 | GRCh38.p7 | 16:69934166 | GCCTAGTTCCCTCCT[A/C/G/T]CTCTCCCTCCTCTTC | 11060 |
rs755202482 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934878 | AGCCCAGAGAGGGCG[C/T]GCCAGTCCATGGGCG | 11060 |
rs755203027 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896979 | CTTTTAAAATCCATT[C/T]GTTTTTATTGTAAAA | 11060 |
rs755227187 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873084 | AATTTGGTAAGTGAC[A/G]CTGAGATAGTTTTCT | 11060 |
rs755244675 | snp | A/G | 5.10904e-05 | 0.00505397 | missense | WWP2 | GRCh38.p7 | 16:69871892 | CGGCACCGCCAGCCC[A/G]TCAAGAACTCAGGCC | 11060 |
rs755244981 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897199 | CCTTGACCTCCCAGG[C/T]TCAGGTGATCCTCTC | 11060 |
rs755259506 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848550 | GCTGAGTTGGGAGGA[-/T]TGCTTGAGCCCAGGA | 11060 |
rs755273957 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825080 | CATCTGTAGCTTTTA[C/T]GTGTATATTTGTGCT | 11060 |
rs755275763 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838639 | AAGTGGCCACTCCCA[C/G]GGATGGCAAGAGGTG | 11060 |
rs755292551 | snp | A/T | 1.64827e-05 | 0.00287073 | missense | WWP2 | GRCh38.p7 | 16:69888045 | CATCTTCAGTGAATG[A/T]TGAACCCACAACAGC | 11060 |
rs755292823 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859564 | TGTCTCAAAAAAAAA[-/G]GAAAAAGAAAAAAAA | 11060 |
rs755307899 | snp | C/G | 1.65562e-05 | 0.00287712 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937619 | CTACCGGCACTACAC[C/G]AAGAACAGCAAGCAG | 11060 |
rs755307917 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888116 | CCACCTGCTGCACCC[C/T]TGAGTGTGACCCCGA | 11060 |
rs755314912 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | WWP2 | GRCh38.p7 | 16:69934083 | CCTCCTCCATCAACC[C/T]GGACCACCTCACCTA | 11060 |
rs755318743 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884842 | CAGGAAGCCAAATAG[G/T]TGATATGGGGAGGTT | 11060 |
rs755327799 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820205 | GCCACTGTACTCCAG[C/G]CTGGGTGACAGAGTG | 11060 |
rs755332488 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882381 | CCTTTGAAACTCACC[C/T]ATTCAATCAAATATC | 11060 |
rs755333952 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855961 | TTCTTGTTTTTAGTG[C/T]TTTTTCTCTTAAAAT | 11060 |
rs755350444 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917432 | CAACATACATCACAT[A/G]TGCACTTCTGGTCCA | 11060 |
rs755365442 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813711 | TGGGCTCTAGTGATC[C/T]TCCCACGTTGGCGTC | 11060 |
rs755380901 | snp | A/G | 1.65452e-05 | 0.00287616 | missense | WWP2 | GRCh38.p7 | 16:69798825 | TGGAATGAGATCATC[A/G]TTTTGTAAGAGAAAG | 11060 |
rs755406501 | snp | C/G | 0.000105313 | 0.00725572 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933213 | CCTCGTCTGCCCAGC[C/G]ACAAACAGCCCAGCA | 11060 |
rs755439660 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771795 | CTAGGACCCAAGTGC[A/G]GGAAGGTGAGTTGGG | 11060 |
rs755441090 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888546 | TGCTTTCCTGAATCA[-/T]TGGAGGATGTTCGCC | 11060 |
rs755450061 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842290 | AGTCCAGAGCTTAGG[A/G]TCCTTATTTATTTTT | 11060 |
rs755455363 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802052 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 11060 |
rs755460282 | in-del | -/TGCACAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883651 | GCCATGGTGGTTTAC[-/TGCACAG]TGCACAGATCAACCC | 11060 |
rs755471485 | snp | A/G | 4.96874e-05 | 0.0049841 | intron-variant | WWP2 | GRCh38.p7 | 16:69937536 | GGGATGCTGACTGCC[A/G]CCTCTCCCCAGCTGA | 11060 |
rs755492819 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765598 | GGAGGCTGAGACGGG[C/T]GGATCACTTGAGGTC | 11060 |
rs755494903 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881936 | GACCTCCAGTGATCC[A/T]CCTGCCTTGGCCTCC | 11060 |
rs755506667 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | WWP2 | GRCh38.p7 | 16:69917746 | CGAGGCAGGTTTTAC[C/T]ATGTGGATCACAATA | 11060 |
rs755522894 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814519 | AATTCCTGTACCCAC[A/G]CCACCATGAAAGGTG | 11060 |
rs755536335 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69772801 | AGTCCTCCCTCCTGC[C/T]TCACCACCAGTGATT | 11060 |
rs755584890 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791608 | CTCACTGCAGCCTCA[A/G]AATAGGCTCAAGCAA | 11060 |
rs755590878 | snp | C/T | 1.64969e-05 | 0.00287196 | missense | WWP2 | GRCh38.p7 | 16:69935932 | ATAAGAGACCAACCC[C/T]GAAAGACCTGGAGTC | 11060 |
rs755608440 | in-del | -/T/TT | 0.443928 | 0.165461 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931493 | TTTAAAGTTCTTTTC[-/T/TT]TTTTTTTTTTTTCAG | 11060 |
rs755610431 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902310 | TGGATTGGGACGTAG[A/G]GTTGGAACATGGTTC | 11060 |
rs755616892 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891078 | TGGGCTGACTCGGGG[C/T]CTGGAGATCGTCAGC | 11060 |
rs755619951 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928080 | TAAGGCAGAGAGTGG[C/G]AGGGAGACTGAGGCC | 11060 |
rs755626161 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869402 | TAATTTTTTTTTTTT[-/G]GTTAAACAAGGTCTC | 11060 |
rs755627426 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760300 | CTTGGATTTGGAGTG[A/G]TACTACAAAAAGTAG | 11060 |
rs755644281 | snp | C/G/T | 3.29925e-05 | 0.00406145 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908873 | ATCAACTGAGAAGAC[C/G/T]TGAGACTCTGGAACT | 11060 |
rs755659304 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | WWP2 | GRCh38.p7 | 16:69939299 | CCTGCTTTGGGAAGG[A/G]ACGTCTCTGCTGACG | 11060 |
rs755713575 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815186 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 11060 |
rs755734366 | snp | A/G | 1.65343e-05 | 0.00287521 | missense | WWP2 | GRCh38.p7 | 16:69917726 | GGGAAAAACGCACAG[A/G]TCCCCGAGGCAGGTT | 11060 |
rs755757247 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817660 | CTTTTTGTTAAACTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTAA | 11060 |
rs755764675 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835804 | ATAAAACCAAAGTAA[A/T]TTTTTTTTTTTTTTT | 11060 |
rs755780737 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862975 | CAAGCAGTCCTCCGC[C/G]CTTGGCCTCCTAAAG | 11060 |
rs755782083 | snp | C/G | 1.853e-05 | 0.00304379 | missense | WWP2 | GRCh38.p7 | 16:69842053 | TCGAGAGACTCCAGT[C/G]GAACAGCAGTAGCTC | 11060 |
rs755782301 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921999 | GAATCGCTTGAACTC[A/G]GGAGGCAGAGGTTGG | 11060 |
rs755794742 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768107 | CTCCCAAAGTGTTTG[A/G]GGTTACAGGTGTGAG | 11060 |
rs755817517 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933469 | TGGATTACATTGTCA[C/T]GGATCGGGGTTGGAA | 11060 |
rs755829083 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910127 | GATCTGTAACCCCCA[A/G]CCTATCCGCCGCACC | 11060 |
rs755840030 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808584 | TTTTTGTATTTTCAG[C/G]AGAGACAGGGTTTCG | 11060 |
rs755842273 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885997 | GGGCAGCCAGATGAT[C/T]GGGAAAGGGGGGTTG | 11060 |
rs755847456 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781192 | GGATAGTTGAACAGT[A/G]AGGAGGCCTGTGTGG | 11060 |
rs755856225 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908350 | GGGTCTATGAAACCC[A/C]GAAATTGCAATACAA | 11060 |
rs755865292 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768027 | CTTTTTTGTAGAGAT[-/G]GGGTCCCACTATGTT | 11060 |
rs755873311 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864022 | AAGCCTCTATGAGCT[C/T]TTGCATACAGGCTTT | 11060 |
rs755910622 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932739 | CAGTAAAACTGTAAC[A/G]GCTTATGTCACCCTA | 11060 |
rs755917410 | in-del | -/TGTCCT | 1.67584e-05 | 0.00289464 | intron-variant | WWP2 | GRCh38.p7 | 16:69930307 | AGCCGAGGCCCAGGC[-/TGTCCT]TGTCCTTGTTCTGGC | 11060 |
rs755931254 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884629 | CAAGACCCTATCTTA[A/G]AAACAAAAAACAAAA | 11060 |
rs755932497 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809445 | GAGGTTGTTTCAGGA[A/G]GGAATTCTAGGATGA | 11060 |
rs755941984 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920439 | CACATTTCAGAGATT[A/G]CTCCTTTTGAGCTGG | 11060 |
rs755945837 | snp | C/G | 4.19745e-05 | 0.00458099 | intron-variant | WWP2 | GRCh38.p7 | 16:69842128 | AGATCCCGGTAAGAC[C/G]CCCCTTGGTGAGGAC | 11060 |
rs755950000 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882696 | TGGGCAAAGAGATGC[A/G]GCAAGAACACAAGGG | 11060 |
rs755956284 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768826 | TCTTTTTCCGTGCTT[A/G]GTCTTTGTAAGGATG | 11060 |
rs755962010 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895150 | AAGGACGACAGCCTT[A/G]TAAGAGTTCTTGGAT | 11060 |
rs755972426 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827696 | AGAGGCGGTTGTGGC[C/T]GCTGCGGTTCCCTGA | 11060 |
rs756014748 | snp | C/T | 1.7038e-05 | 0.00291868 | intron-variant | WWP2 | GRCh38.p7 | 16:69937094 | GGGTCTCAGACTCCA[C/T]CCATGGCTGCTCTTT | 11060 |
rs756020529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797853 | AGATTGTGGCATTAC[A/G]CTCCAGCCTGGGCAA | 11060 |
rs756021397 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771122 | TAGCCTCCAGAAGAT[G/T]GACAGGTCTGAAAGG | 11060 |
rs756069959 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829360 | AACCCTTTAGCACTG[C/T]GCAGTGGCTCTTAGG | 11060 |
rs756098646 | snp | C/T | 2.21668e-05 | 0.0033291 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939959 | AGGCCGCCCCTCCCA[C/T]GCCCCCCAGCGCACA | 11060 |
rs756100418 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789283 | TGCTCAGGCTGGAGT[C/G]CAGTGGTGCGATCTC | 11060 |
rs756111653 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922738 | TCCTTCTGGCTTTAT[-/AA]TTTTCAAGTTGTACT | 11060 |
rs756144699 | snp | A/G | 3.29478e-05 | 0.00405867 | missense | WWP2 | GRCh38.p7 | 16:69888132 | TGAGTGTGACCCCGA[A/G]TCCCAACACGACTTC | 11060 |
rs756144906 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859535 | CACTCCAGCCTGGGC[A/G]ACAGAGGGAGACCCT | 11060 |
rs756145419 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918728 | TCCAATCCATCTGGC[C/T]TGTTCCCCTCAGAGC | 11060 |
rs756145808 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896035 | TTATTTCCAAAGATT[C/T]TACTGTTGTCGGAGG | 11060 |
rs756153846 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816971 | GATTTAACCCAGTTC[C/T]TTTGTTCCTAGAGTC | 11060 |
rs756155464 | snp | A/C/G | 3.29548e-05 | 0.00405913 | intron-variant | WWP2 | GRCh38.p7 | 16:69840103 | CTCTTTAGCCCATCC[A/C/G]TGTTGCCTTTTGTAC | 11060 |
rs756168745 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858701 | TAGTATTGGAATCAG[A/T]GAAGAATTGACACAT | 11060 |
rs756192129 | snp | G/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69776214 | AAGGCTAAAGAGGGC[G/T]GGAGTCAGGGGACTT | 11060 |
rs756204622 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804169 | TTCTAACTTTGTATG[G/T]TTTTAACTTTCTGTA | 11060 |
rs756238979 | in-del | -/CCA | | | intron-variant, cds-indel | WWP2 | GRCh38.p7 | 16:69909503 | TGTGCCACACACATC[-/CCA]CCTCATCTTCTGGTC | 11060 |
rs756243591 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818205 | TTATTTATTTATTTA[A/G]TTTATTTATTTTATT | 11060 |
rs756252991 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879582 | GCTGAATAATATTCC[A/G]TTGTATATACATACC | 11060 |
rs756301824 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787152 | CTAACCACACCTTGG[C/T]CTGGGGAGCCAAATT | 11060 |
rs756318143 | snp | A/C | 3.29484e-05 | 0.00405871 | missense | WWP2 | GRCh38.p7 | 16:69840198 | CAGGCGGAGAGCTGA[A/C]AATTTTCCTGGACGG | 11060 |
rs756321218 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763839 | TAAAAGTCACACCGG[C/T]GTAAGTGGTGACAAA | 11060 |
rs756348437 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848195 | GTGCAGGCTGGGTGT[A/G]ATCCCAGCGCTTTGG | 11060 |
rs756366874 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911791 | TTAAAAAGGCATAAA[C/T]CTTCAACAATAAAGG | 11060 |
rs756372269 | in-del | -/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760498 | ATGCCCGGCGAATCT[-/T]TTTTTTTTTTTTTTT | 11060 |
rs756374389 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895593 | ACATAGCAAGACTTC[A/G]TCTCTACAAAAAATA | 11060 |
rs756374932 | snp | A/C | 9.49172e-05 | 0.00688837 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933199 | TGCGTCGACGGACTC[A/C]TCGTCTGCCCAGCCA | 11060 |
rs756375790 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853353 | AACTACTGTGCCCTT[-/G]GCAACCGCTTTATGT | 11060 |
rs756410522 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935675 | TAGGTACAAGTCAGG[A/G]TAAAGGCGTTGTTTA | 11060 |
rs756411124 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765048 | GTCTCTACAAAAAAT[A/G]CAAAAATTAGCCAGG | 11060 |
rs756413601 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786138 | CTTTTTGGAGATGTC[-/TT]TTTTTTTTTTTTCTT | 11060 |
rs756428956 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840922 | TTCTGTAGCTTCAAA[G/T]GGGTGCAATTTGAAT | 11060 |
rs756435168 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935059 | GGGAGGTCCTGCCAC[A/G]TGCCCCGTTGAGGGT | 11060 |
rs756438564 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835762 | TCTCATCTACTCTTG[A/C]GTCTCCCAAGAATAA | 11060 |
rs756451733 | snp | A/T | 1.68272e-05 | 0.00290057 | intron-variant | WWP2 | GRCh38.p7 | 16:69929430 | ATCTGATGTTCTTTC[A/T]TTCTTCTCATGTGGC | 11060 |
rs756464928 | snp | C/T | 1.6582e-05 | 0.00287936 | intron-variant | WWP2 | GRCh38.p7 | 16:69937516 | GCGCGGGGAGGGACC[C/T]GCCGGGGATGCTGAC | 11060 |
rs756472366 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795831 | TTTTGTATTTTTGGT[A/G]GAGACAGGGTTTAGC | 11060 |
rs756475186 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865111 | CTGGAGTGCAGTGGC[C/G]TGATCTCGGCTCACT | 11060 |
rs756478118 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873268 | AGTTCTGTGGCAGCA[C/T]CATATGGGGGCTTCA | 11060 |
rs756482091 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822993 | AGTACAAAAATTAGC[C/T]AGGCATGGTGGCACG | 11060 |
rs756483405 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931915 | AGTGCCCCGGAAGGC[A/T]GCCCTGTACCCCGCT | 11060 |
rs756528411 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837327 | TACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 11060 |
rs756553071 | snp | C/T | 1.66629e-05 | 0.00288638 | intron-variant | WWP2 | GRCh38.p7 | 16:69937269 | TGCTGGGACCCTGAG[C/T]CCCTGCCTCTGGGGC | 11060 |
rs756561198 | snp | G/T | 1.87369e-05 | 0.00306074 | missense | WWP2 | GRCh38.p7 | 16:69871924 | CAGTGGCTTGGCCAA[G/T]GGCACAGGTGAGTGA | 11060 |
rs756566153 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800411 | AGCCTCACATTAGGA[C/T]GCAGCAACCAGCATG | 11060 |
rs756572926 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906483 | GTAATATCTATCAGT[A/G]TAGATACATCAGGCT | 11060 |
rs756573449 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833891 | CCTGGCTGATGTGCT[C/T]GGTGGGGAGTCCTGG | 11060 |
rs756583448 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783180 | ATGCCCGGCTAATTC[G/T]TGTATTTTTAGTAGA | 11060 |
rs756588837 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812852 | GTGTCAGGTTTTTCC[A/G]CTGCAAAATTACTGT | 11060 |
rs756610751 | in-del | -/TTGCTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793908 | GGGCTGTTATTATCC[-/TTGCTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs756653204 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | WWP2 | GRCh38.p7 | 16:69888030 | AAAGTATGATTTGTG[C/T]ATCTTCAGTGAATGA | 11060 |
rs756685013 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855691 | GGGGAAAGAGAGTTT[A/G]GGCAGAAGAATGGCT | 11060 |
rs756687962 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784320 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 11060 |
rs756711130 | snp | A/G | 4.95111e-05 | 0.00497525 | intron-variant | WWP2 | GRCh38.p7 | 16:69936275 | GAAAGACCCTGACAC[A/G]GTAGACATCTCCCCA | 11060 |
rs756734868 | snp | A/G | 1.6525e-05 | 0.00287441 | missense | WWP2 | GRCh38.p7 | 16:69798813 | TCTGAGCTTCTCTGG[A/G]ATGAGATCATCATTT | 11060 |
rs756763602 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892734 | AGACAAGGTCTCCCT[A/G]TGTTTCCAAGGCTGG | 11060 |
rs756764558 | snp | A/G | 3.43826e-05 | 0.0041461 | missense | WWP2 | GRCh38.p7 | 16:69939041 | GGTGGTGAAGGAGAT[A/G]GACAACGAGAAGAGG | 11060 |
rs756777104 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817583 | TTGTATAAATGTACC[C/T]ACAGTTTAACCAGTC | 11060 |
rs756781225 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843848 | GGTAACAGAGTGAGA[C/G]TATGTCTGTAAAAAA | 11060 |
rs756794603 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844387 | ATTTCACTCTTTAGA[A/G]AGTGATGCCTTCTCA | 11060 |
rs756797873 | snp | C/G | 1.65015e-05 | 0.00287237 | missense | WWP2 | GRCh38.p7 | 16:69798712 | CCAAGGTGCATAATC[C/G]TCAACCTCGAATTAA | 11060 |
rs756809259 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790569 | AACTGTATGATGTTT[A/C]GCATCTTTTTTTTTG | 11060 |
rs756809457 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867059 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 11060 |
rs756814812 | snp | A/C/G | 0.000119738 | 0.00773666 | intron-variant | WWP2 | GRCh38.p7 | 16:69929407 | GGACACCGGCTCTCC[A/C/G]TGTTTGAATCTGATG | 11060 |
rs756824043 | in-del | -/GT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822534 | TGGCCTGGGTGGGGT[-/GT]GTGTGTGTGTGTGTG | 11060 |
rs756824840 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877721 | TTAGAGGCCAATGTA[-/G]GGTATAAGGAGAGAG | 11060 |
rs756828417 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773826 | ATGCAAATTTTTTGC[A/G]TTTTTTTAGTTCAGC | 11060 |
rs756837378 | snp | A/G | 1.66665e-05 | 0.00288669 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931883 | CTGGACTATGGGGGC[A/G]TCGCCAGGTGAGCTT | 11060 |
rs756841617 | in-del | -/TGAACAAGTCAATATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899950 | TATATTGTAAATACC[-/TGAACAAGTCAATATT]TGAACAAGTCAATAT | 11060 |
rs756851281 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891748 | CTCCTGACTCACTAC[C/G]TGGACAGTTCCATGT | 11060 |
rs756866745 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761879 | TACTCAATTCAATTT[C/G]ATCTTCAGATAATCA | 11060 |
rs756875696 | in-del | -/CACACACT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883421 | ACACACACACACACA[-/CACACACT]CATTTACTCCTACTT | 11060 |
rs756895104 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791515 | TTACAGGCGTAAGCC[A/G]CTGCACCTGGCCTCT | 11060 |
rs756906621 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831079 | GAAGAAGGAGGCTTG[C/T]TTCACTAAGCAGGTC | 11060 |
rs756907156 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861888 | AGCTATTAAAAGACA[A/G]TGACCAGTTAAGAGT | 11060 |
rs756908595 | snp | C/T | 4.76679e-05 | 0.00488177 | intron-variant | WWP2 | GRCh38.p7 | 16:69939012 | CTGACTGTGCCTTGA[C/T]TTGCGGACTTCCAGG | 11060 |
rs756917143 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909998 | TGACTTATTGTTTTT[A/G]GCTGTTTTTGTACTT | 11060 |
rs756922204 | in-del | -/TT | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760497 | CATGCCCGGCGAATC[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs756927331 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908857 | TCCTCCAGGGTAGGT[C/T]ATCAACTGAGAAGAC | 11060 |
rs756937665 | in-del | -/ATT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765950 | TTACAGGCATGAACC[-/ATT]GCACCTGGCTCAGTC | 11060 |
rs756957514 | in-del | -/TTTGTTTGTTTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912568 | AAATTGGAGGGTAGT[-/TTTGTTTGTTTG]TTTGTTTGTTTTTGC | 11060 |
rs756976576 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806952 | ATTTATTTATTTATT[-/CA]TATTCATTCATTCAT | 11060 |
rs756989147 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877458 | CAGACTACTCCCTAT[C/T]GCTTTCTCCCTATCA | 11060 |
rs756992104 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901090 | TAAACACAGTGCACA[A/G]GAATTATATTCCACT | 11060 |
rs757014863 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937786 | CCTTGCAAAAGGAGA[C/T]GATAGACCAGCCTTG | 11060 |
rs757067247 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884912 | TGTGGTAGAATTAGA[A/C]TATTACTATTTTGCA | 11060 |
rs757103138 | snp | C/T | 8.24219e-05 | 0.00641905 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936405 | CGAGCTGAAGGAGGG[C/T]GGCGAGAGCATCCGG | 11060 |
rs757108701 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886852 | GTAAGAAACGTTCAC[A/G]AAGAATCTGGATAGC | 11060 |
rs757130733 | snp | A/C/G | 6.59798e-05 | 0.00574336 | missense | WWP2 | GRCh38.p7 | 16:69840261 | GCAGTGCCCTGACAG[A/C/G]TGGTGAGTGCCGCCC | 11060 |
rs757131269 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808461 | GGCTGGGGTGCAATG[G/T]TGCAATCTTGGCTCA | 11060 |
rs757131841 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888348 | TATTACCTAGTGGCT[A/G]GTAGCCTCTGGGGAG | 11060 |
rs757136255 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922184 | GTTTCTTACTCTGCA[A/G]TGAGCCCCTTGCATT | 11060 |
rs757192511 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768050 | ACTATGTTACTCAGA[C/G]TGGTCTTGAACTCCG | 11060 |
rs757200917 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896142 | TTTCCTTTTTTTGGA[C/G]ACAGGGTCTCATTTT | 11060 |
rs757263773 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809265 | CGTACGTAGCCTATG[C/T]ACCTAACATTCCAGC | 11060 |
rs757310263 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802207 | TGCTGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 11060 |
rs757317101 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787962 | TAGTCCAGGCCACCA[C/T]TGTCTCCACCCTGAG | 11060 |
rs757334595 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905980 | TGTTAGCCTGTAGCT[C/T]GTGGTAGATTCTCAG | 11060 |
rs757346508 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879669 | GCTGTTGGAATAATG[A/C]GGGTGAGAACTTGGC | 11060 |
rs757374656 | snp | G/T | 5.02803e-05 | 0.00501374 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933080 | GTGGCCGCGCCCTGT[G/T]TGTGTCTCTCTCTGT | 11060 |
rs757429642 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829234 | TTTCATCTGCAGCCT[C/T]CTGTCTGCTCTGCCT | 11060 |
rs757434299 | snp | A/C | 1.66205e-05 | 0.00288271 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799291 | GAAGAACAATGGGGG[A/C]AAAAGTACGTATGAT | 11060 |
rs757443192 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824864 | CAGCCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 11060 |
rs757454843 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69774799 | ACTTGGTAAAATCCT[A/C]TCTCTACTAAAAATA | 11060 |
rs757456341 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768819 | CGTTTTCTCTTTTTC[C/T]GTGCTTAGTCTTTGT | 11060 |
rs757458810 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880665 | TCCCATGCCGTGCTA[A/G]TTACGAAATCTTTGT | 11060 |
rs757464706 | snp | C/T | 1.65389e-05 | 0.00287562 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937223 | GCTGCGCTACTTTGA[C/T]GAGAAAGAGCTGGAG | 11060 |
rs757492444 | in-del | -/TGAT | 0.000102889 | 0.00717173 | intron-variant | WWP2 | GRCh38.p7 | 16:69842006 | TTCTGTCTTTTCTTG[-/TGAT]TGATTCCTTTCTAGG | 11060 |
rs757497261 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919080 | AACTCCTGACCTCAA[A/G]TGACCTGCCCTCCTC | 11060 |
rs757524818 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | WWP2 | GRCh38.p7 | 16:69840096 | GTGCATTCTCTTTAG[A/C]CCATCCATGTTGCCT | 11060 |
rs757548759 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927377 | CCCACACACTGCTGT[A/G]GGACTCAGGACACCT | 11060 |
rs757632888 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936588 | TTGATGGTGGCTGCT[G/T]GTGGGCGGTCATGTG | 11060 |
rs757641576 | snp | A/G | 6.58935e-05 | 0.00573955 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931209 | GTGGAAGTATCACCA[A/G]TTCCGTTTCCTCTGC | 11060 |
rs757653786 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763732 | TAGATTGCAAATCCT[C/T]CAAGGGCAGGTTTCA | 11060 |
rs757662562 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864243 | CATGGTGGTGCGCAC[C/T]TGTGATCCCAGCTAC | 11060 |
rs757731089 | snp | A/G | 3.30158e-05 | 0.00406286 | missense | WWP2 | GRCh38.p7 | 16:69935908 | TCCCTTTCTACAAGC[A/G]GATGCTCAATAAGAG | 11060 |
rs757733286 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898225 | TAGAGACAGGGTTTC[A/G]CCATGTTAGCCAGGG | 11060 |
rs757781400 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769063 | GTGGCTCACGCCTGT[A/T]ATCCCAGCACTTTGG | 11060 |
rs757805460 | snp | A/G | 3.34818e-05 | 0.00409143 | missense | WWP2 | GRCh38.p7 | 16:69871850 | ACAACCCCAGCAACC[A/G]GCGAGCAAAGCCCCG | 11060 |
rs757807584 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | WWP2 | GRCh38.p7 | 16:69925507 | CTGAGTTCTCTTCCT[A/G]GCCCTTGGCCTTCCG | 11060 |
rs757821005 | snp | C/G | 1.77005e-05 | 0.00297489 | intron-variant | WWP2 | GRCh38.p7 | 16:69935811 | GGTCTTGGCAGTGCC[C/G]AGGGAAGGCCAAACC | 11060 |
rs757828954 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865363 | CCTCAAATCTTTTGA[A/T]TATTTAAAAAATATT | 11060 |
rs757836103 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932115 | CAGGTGGATCACCTG[A/T]GGTCGGGGGTTCGAG | 11060 |
rs757843422 | snp | C/G | 3.37467e-05 | 0.00410758 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939113 | CGTCGGGGGATTTGC[C/G]GAACTCATCGGTATG | 11060 |
rs757851530 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856960 | AACAGCATTTAACTA[C/G]AGTTTTAAAAAACCA | 11060 |
rs757861352 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904637 | TAGCCTCCCAAAGTT[C/G]TGGTACTGTAGGCAT | 11060 |
rs757865641 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783114 | TTCCCAGGTTCAAGC[A/G]ATTCTTCTGCCTCAG | 11060 |
rs757865673 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884221 | GCACTTTTTCGTTTA[C/G]TAGTTATCTTAGAAT | 11060 |
rs757876546 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823960 | CGTGTAGCATTCAGG[C/T]CCTAAATGAACACCT | 11060 |
rs757876636 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811454 | CACCCCTCCATCCCT[A/G]CAAAAAATAAAAAAA | 11060 |
rs757889044 | in-del | -/ATC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933742 | CACGTTTTCCCAAAT[-/ATC]ATCCTCAAATGCAGT | 11060 |
rs757918597 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854202 | ATAAAAAGAGTATGG[A/G]TGTTGGAGAAATGAC | 11060 |
rs757953808 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894328 | TCAAGCGATCTTCCC[A/G]CCTTGGCCTCCCAAA | 11060 |
rs757963038 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893006 | TGGGATCCACTCCAC[A/C]TCTCTGCCTAAGCCA | 11060 |
rs757981260 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776435 | CACCAAAACCAGTGC[A/G]GAGTACATAATAGAT | 11060 |
rs757983006 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919005 | CCCACCACCACACCC[A/G]GCTAATTTTTGTATT | 11060 |
rs757989650 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799837 | ATCTGAATTAGCCAA[C/T]GTGCCTCTACGTCAC | 11060 |
rs758007669 | snp | C/G | 3.32657e-05 | 0.0040782 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931781 | AGAGTGGCAGGCTGG[C/G]CCGATGCTCTGTCTT | 11060 |
rs758026411 | snp | G/T | | | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939886 | GAGCTACGAACAGCT[G/T]AGAGAGAAGCTGCTG | 11060 |
rs758066867 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842694 | TTGTTTTTTGATATG[C/G]GGTCTTGCTTTGTTG | 11060 |
rs758075246 | in-del | -/GTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876354 | GGCATGTTTTTTGGG[-/GTTT]TTTTTTTTTTTCGTT | 11060 |
rs758091198 | snp | C/T | 3.31384e-05 | 0.00407039 | intron-variant | WWP2 | GRCh38.p7 | 16:69798677 | TTTCTTTCTTTCTCT[C/T]CCAGTGGTGTCCGCA | 11060 |
rs758095666 | snp | A/G | 4.94686e-05 | 0.00497311 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931589 | CCAACAGGTTAGATC[A/G]TGGTGCCCGAAACCA | 11060 |
rs758108489 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818564 | TCTGCTGCATTTGCT[C/T]GTCCCAAGGTCGCCA | 11060 |
rs758117633 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903054 | GGTGATGGAAGAAAG[A/G]TCTTGTTCCTCTGGC | 11060 |
rs758130246 | in-del | -/TTAGAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883312 | GCCAGTAATGTATTG[-/TTAGAA]CTTAATTTCTGCTGA | 11060 |
rs758151060 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843632 | AGCTCTTTTGGAAGA[C/T]CAAAGTGGGAGGATC | 11060 |
rs758154753 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830511 | AGACCAAAACTTTAA[G/T]TTAGCAATGATAAAG | 11060 |
rs758160964 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930072 | AGGACCCAGCCTCCA[A/G]CCACCAAGGTCCAGA | 11060 |
rs758161938 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867453 | TGAGTACATTTCAGC[A/G]GCCCTCATGAAGGGC | 11060 |
rs758167956 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888756 | GTCACCCAGGCTGGA[G/T]TGCAATGGCACGATC | 11060 |
rs758178676 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810890 | CTCCTGAGCAGGTGG[C/G]ATTACAGGTTCACAC | 11060 |
rs758199264 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911486 | TTTGGGGAAGGATGC[A/G]TGGGGTGGTTATGCT | 11060 |
rs758219208 | snp | A/G | 8.31753e-05 | 0.00644831 | intron-variant | WWP2 | GRCh38.p7 | 16:69939442 | TTTTAGTGGGAGGTC[A/G]GGGGGCCTCAGACCC | 11060 |
rs758219262 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867857 | CTAAATGGTGAGGGG[A/G]CTTGGGCCAAGGTTG | 11060 |
rs758221040 | snp | C/T | 4.95438e-05 | 0.00497689 | intron-variant | WWP2 | GRCh38.p7 | 16:69939316 | CGTCTCTGCTGACGT[C/T]GGCGTGTTTTACCTT | 11060 |
rs758242885 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830978 | TTTGCAGTTATGTGT[A/G]GAATGAACACGGGCC | 11060 |
rs758252229 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878574 | ATTTTGTTGCCCAGG[A/C]CGGTCTCCAACTCCT | 11060 |
rs758253819 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791428 | AGACAGGGTTTCACC[A/G]TATTGGTCAGGCTGG | 11060 |
rs758264579 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808931 | TGGATGTATGCTTAC[C/T]TTTAGTAGACACCAT | 11060 |
rs758272566 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899726 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 11060 |
rs758279296 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861566 | GGAGCCGTAAATTGC[A/G]CTTGCAGTGACCAGA | 11060 |
rs758279520 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842817 | TGAGACAGCAGGCAT[G/T]TGCCACCATGCCTGG | 11060 |
rs758282875 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819236 | TGCTGTTGTCTTCCT[A/G]TGGAACGGTTCTGAA | 11060 |
rs758285921 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | WWP2 | GRCh38.p7 | 16:69908751 | TGCTACCCTTGACTT[C/T]ATTTTTCAGATGGGA | 11060 |
rs758308251 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777490 | GTTTTTAGTAGAGAT[A/G]GGGTTTCACCCTGTT | 11060 |
rs758313256 | snp | A/C | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925398 | AGTGGCTTTTTGTAA[A/C]CTCTGTGTTCTGCTG | 11060 |
rs758335524 | snp | C/T | 0.000143328 | 0.00846425 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933192 | CACCCTCTGCGTCGA[C/T]GGACTCCTCGTCTGC | 11060 |
rs758374464 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807400 | GTCTTTGAATTTTCA[C/T]CCCTGGATATTGAAT | 11060 |
rs758377169 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | WWP2 | GRCh38.p7 | 16:69908840 | ACCTGGGAGCGGCCC[C/T]TTCCTCCAGGGTAGG | 11060 |
rs758393272 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838842 | CCATGGCAGGGAAGA[A/G]AGATTAAGGGAAGGT | 11060 |
rs758394771 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778885 | CCCTCAAGTGATCCG[C/T]ATGCCTGAGCCTCCC | 11060 |
rs758404167 | snp | C/G | 1.65119e-05 | 0.00287327 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929461 | AGAGAAGAGACAGGA[C/G]AATGGACGGGTGTAT | 11060 |
rs758452298 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782928 | CTCTTGCCGCAGCCT[C/T]CCAGTGTGCTGGAAT | 11060 |
rs758495919 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922461 | CCCAACCCAGGGACC[A/C]TTACCCGGGAAGAGG | 11060 |
rs758496677 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766505 | CCTGCAAGCCTTCCA[C/T]GACCTGATCTCTCCT | 11060 |
rs758516062 | snp | A/G | 1.65633e-05 | 0.00287774 | missense | WWP2 | GRCh38.p7 | 16:69937144 | ACTGGCGTTTCACCC[A/G]AGGCGTGGAAGAGCA | 11060 |
rs758539749 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804141 | TAAATGTTTTTCTAG[C/T]TTTTCATTTGCATTC | 11060 |
rs758575255 | in-del | -/C | 4.15822e-05 | 0.00455954 | intron-variant | WWP2 | GRCh38.p7 | 16:69842126 | AAGATCCCGGTAAGA[-/C]CCCCCCTTGGTGAGG | 11060 |
rs758591694 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806126 | GGATCACTTGAGTCC[A/G]GGATTCTGAGGCTGC | 11060 |
rs758596847 | snp | A/G | 1.6884e-05 | 0.00290547 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939901 | GAGAGAGAAGCTGCT[A/G]TATGCCATTGAGGAG | 11060 |
rs758604668 | snp | C/T | 2.34915e-05 | 0.00342713 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939969 | TCCCACGCCCCCCAG[C/T]GCACATGTAGTCCTG | 11060 |
rs758611519 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882247 | AGGTGTGAACCACTG[C/T]GCCCAGCCTAAAGAA | 11060 |
rs758611900 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870727 | TTGAAACATCTCACA[A/G]TTGCAAAGTAGTAGA | 11060 |
rs758619089 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906173 | CGCCTTCCGGGTTCA[C/T]GCCATTCTCCTCCCT | 11060 |
rs758619215 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931104 | AAAGACAAATTGTTC[A/G]TTTTCTGAGAAATCG | 11060 |
rs758626723 | in-del | -/T | 1.67626e-05 | 0.002895 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931488 | CTCGATTTAAAGTTC[-/T]TTTTCTTTTTTTTTT | 11060 |
rs758627189 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931193 | ATGACCGCAGTTTTC[A/G]GTGGAAGTATCACCA | 11060 |
rs758682556 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858514 | CAGAGAAGAGGGGGC[A/G]CCCTTTATCACAGCC | 11060 |
rs758691107 | snp | A/G | 1.6569e-05 | 0.00287824 | missense | WWP2 | GRCh38.p7 | 16:69799284 | ACGTCTTGAAGAACA[A/G]TGGGGGCAAAAGTAC | 11060 |
rs758701872 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787815 | ACATCTAAAATTTAG[C/T]CTGTCTATAGCTGAG | 11060 |
rs758705368 | snp | C/G/T | 3.32747e-05 | 0.00407878 | intron-variant | WWP2 | GRCh38.p7 | 16:69934176 | CTCCTCCTCTCCCTC[C/G/T]TCTTCCCTCTCCTGG | 11060 |
rs758708587 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916525 | TTAATTCTGGGGTAG[A/G]AGCAGTAGTCCAGGG | 11060 |
rs758717332 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891005 | GGTGTCGGAGACCCA[A/G]TTTTCCAACCCAGAT | 11060 |
rs758718549 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813732 | CGTTGGCGTCCCAAA[A/G]TGCTGTGGGATTACA | 11060 |
rs758723057 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773026 | GGAACAGAGATAAAT[G/T]TATGTGTAGTCTGCT | 11060 |
rs758723491 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818224 | ATTTATTTTATTTTT[A/G]TGAGATGGAGTCTTG | 11060 |
rs758740519 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839959 | GTGATTTCATTAGAC[A/G]TATTCCTTCCCACTC | 11060 |
rs758769060 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929163 | TGTGCTGCTCCCTCT[C/G]GGTGGCCACACCACC | 11060 |
rs758770682 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846203 | TAAAGAAAGAGTTAT[A/C]TCATAAATTGTCATA | 11060 |
rs758801127 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761982 | GAAATTCAAATTTAA[A/G]TGGGTGTCCTGTACT | 11060 |
rs758807244 | snp | C/T | 1.65179e-05 | 0.00287379 | missense | WWP2 | GRCh38.p7 | 16:69917830 | CAGTGGCAGTCGCAG[C/T]GGAATCAGCTCCAGG | 11060 |
rs758814955 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760424 | ACCTCCGCCTCCCGG[C/G]TTCAAGCAATTCTCC | 11060 |
rs758827561 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69910924 | ATGGCTCACCTGTAC[A/G]CCCTGCATAGCTTAC | 11060 |
rs758834164 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792568 | CTGCTGATTAACTGT[A/G]GGTTACAAATGTGTC | 11060 |
rs758836126 | in-del | -/ATACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820824 | CATGAATACATGCAT[-/ATACAC]ACACACACACACACA | 11060 |
rs758842944 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833207 | CAAACAAGATTGATA[C/T]ATCTTTTCAGTCTCT | 11060 |
rs758890466 | snp | C/G | 2.68482e-05 | 0.00366379 | intron-variant | WWP2 | GRCh38.p7 | 16:69842168 | AGAAGTTGCTTAGAG[C/G]TATTGAAAACATGTT | 11060 |
rs758891090 | snp | A/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784701 | AAAAGCTCTTCTGCC[A/G/T]CCTGTTGAAGTATAA | 11060 |
rs758894705 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802973 | ATCCAAAACACTTCC[A/T]GTCCCAAGCATTTCA | 11060 |
rs758903595 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | WWP2 | GRCh38.p7 | 16:69934091 | ATCAACCCGGACCAC[A/C]TCACCTACTTTCGCT | 11060 |
rs758933862 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880888 | TGAGTGTCCACCACG[A/T]GTCTGTGATACACCA | 11060 |
rs758959430 | snp | C/T | 3.37507e-05 | 0.00410782 | intron-variant | WWP2 | GRCh38.p7 | 16:69937661 | CTGGCAGGTGGGTCC[C/T]GGGCCCAGGCCTTGG | 11060 |
rs758984962 | snp | A/G | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933539 | TAGAGTGGAAACAGG[A/G]TAGTTACTATTCAAA | 11060 |
rs758995885 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886741 | CTCCAGCTTGGGTGA[C/T]GGAGCGAGACTGTGT | 11060 |
rs758996419 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913284 | GTGAGCCACCCACCT[C/G]GGCCTCCCAAAGTGG | 11060 |
rs759007027 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794472 | AGGTGGAGGCTGCAG[C/T]GAGATGAGATTGCAC | 11060 |
rs759008625 | snp | A/G | 1.79809e-05 | 0.00299836 | intron-variant | WWP2 | GRCh38.p7 | 16:69917918 | GCCCGAGGTGGGGCC[A/G]CCTCCCTGCGCTTGC | 11060 |
rs759018558 | in-del | -/A | 1.66362e-05 | 0.00288406 | intron-variant | WWP2 | GRCh38.p7 | 16:69939442 | TTTAGTGGGAGGTCG[-/A]GGGGGCCTCAGACCC | 11060 |
rs759026185 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863344 | TAGTCACTATCATAA[G/T]CAAGATACAGAAAGG | 11060 |
rs759076647 | snp | A/G | 1.73369e-05 | 0.00294417 | intron-variant | WWP2 | GRCh38.p7 | 16:69917915 | TTGGCCCGAGGTGGG[A/G]CCGCCTCCCTGCGCT | 11060 |
rs759083316 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856204 | CTTAAGAAGCCAGAC[A/T]TAGAAGCTTATGTTC | 11060 |
rs759088222 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | WWP2 | GRCh38.p7 | 16:69930216 | TGGACCACAATACCC[A/G]CACCACCACCTTTAA | 11060 |
rs759101884 | in-del | -/TTTATTTATTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866279 | TTCACATTTTATTTA[-/TTTATTTATTTA]TTTATTTATTTATTT | 11060 |
rs759126941 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824126 | CAGTCATTCGGGCGG[C/T]TTCCGCCTGACCGTC | 11060 |
rs759132403 | snp | C/T | 4.21692e-05 | 0.0045916 | intron-variant | WWP2 | GRCh38.p7 | 16:69939824 | GGCTGACTGTCGTGC[C/T]TCCCCACTCTCAATA | 11060 |
rs759168746 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900368 | TGCAGTGGCTCACGC[C/G]TGTAATCCCAGCACT | 11060 |
rs759188858 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932674 | GATAAGCTGTGTCAC[A/G]ATCCACAGGGCCTTG | 11060 |
rs759208366 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801906 | TTTCTCTTTAAAAAT[A/G]TATCAATATATATTT | 11060 |
rs759213537 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905732 | TCACTTTGAGATCAG[A/G]ATTGGGAAGCCACCT | 11060 |
rs759246601 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940814 | GCAGGCCTGACCCGG[C/T]GGCACAGCCTGGCAG | 11060 |
rs759263594 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934033 | TTTATTTGAATATGC[C/T]GGAAAGAACAATTAC | 11060 |
rs759273655 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914971 | GGATGCAAGACACAG[A/G]GAACTTAACCCCGAG | 11060 |
rs759284028 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825851 | AGGCTGGTCTCAAAC[A/T]GGGCTCAAGGGATTT | 11060 |
rs759290018 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890803 | AACGCTCTTTATTCT[A/G]AGTCTGGCAGATCGA | 11060 |
rs759327057 | snp | C/T | 0.000136059 | 0.00824688 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871891 | CCGGCACCGCCAGCC[C/T]GTCAAGAACTCAGGC | 11060 |
rs759338290 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812310 | AGCTGGGATTACAGG[C/T]ACCCACCATCATGCC | 11060 |
rs759379928 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900101 | ATGACGTAACAGATG[C/T]ACTTATAGCTAAATT | 11060 |
rs759387061 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855129 | TGGGATTACAGGCAT[G/T]AGCCGCTGAGCCCCA | 11060 |
rs759389920 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800481 | TTTTGCTTTTGGTTA[A/G]CAAAAGTCCTTGTAG | 11060 |
rs759412417 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830885 | TCTGAGTTTCAGGGA[A/G]CTGGGGAATGGAAAG | 11060 |
rs759419131 | snp | C/G | 3.33578e-05 | 0.00408384 | intron-variant | WWP2 | GRCh38.p7 | 16:69798633 | GCCACAGGGGGGCAT[C/G]TGGGAGCCCTGGGAC | 11060 |
rs759419201 | snp | C/T | 2.42721e-05 | 0.0034836 | intron-variant | WWP2 | GRCh38.p7 | 16:69871960 | CCGCACGCCAGCCTG[C/T]ACTGAAGCTGTGGGC | 11060 |
rs759476857 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856303 | TGTGGGGGCATTGGA[G/T]GAGGGATTGACTGCA | 11060 |
rs759480193 | in-del | -/G | 1.65858e-05 | 0.00287969 | intron-variant | WWP2 | GRCh38.p7 | 16:69929540 | CAGGGGTAAGGACTT[-/G]GGCTGAGAGGGGGGC | 11060 |
rs759481408 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882390 | CTCACCTATTCAATC[-/A]AATATCTTTCTTTTG | 11060 |
rs759506132 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889787 | GTGTCACTCTAGTTG[C/T]TGGTGATCTGGTTGA | 11060 |
rs759515828 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927195 | CTGAATCTCAGATCC[C/T]TGGGGATCTGTGTTG | 11060 |
rs759530324 | snp | G/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761111 | GAGTGAAACTCTGTC[G/T]CAAGCAAGCAAATAA | 11060 |
rs759533708 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911947 | ATGTGCACCATGGGG[A/C]TCTGGAAAGCCTCAG | 11060 |
rs759563507 | snp | C/T | 1.66192e-05 | 0.00288259 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935879 | TGGAAAGTTCATCGA[C/T]ACGGGCTTCACCCTC | 11060 |
rs759564626 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844221 | GTTGGGTCTCACGGG[A/G]TGATGAATGACAGTG | 11060 |
rs759595712 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898571 | CTGATTACTATTGAG[A/C]TTGAACCTCTTTTTA | 11060 |
rs759609593 | snp | A/G | 8.24137e-05 | 0.00641873 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936411 | GAAGGAGGGCGGCGA[A/G]AGCATCCGGGTCACA | 11060 |
rs759622547 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875875 | CCTGTTGTGTTGATA[C/T]GTTGACCTCCTCCCA | 11060 |
rs759626310 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931174 | CAAGGTTCCCCTGGT[G/T]CTTATGACCGCAGTT | 11060 |
rs759653665 | snp | A/G/T | 9.59811e-05 | 0.00692697 | missense | WWP2 | GRCh38.p7 | 16:69939099 | ACCTGCCGCCTGCCC[A/G/T]TCGGGGGATTTGCCG | 11060 |
rs759662819 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886589 | ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 11060 |
rs759693369 | snp | A/G | 2.10666e-05 | 0.00324544 | missense | WWP2 | GRCh38.p7 | 16:69842024 | TTGATTCCTTTCTAG[A/G]ATCACAGCTGCCTTC | 11060 |
rs759716765 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819804 | ACTGAGTCATGCAGT[C/T]ATTGCCATGAATTTT | 11060 |
rs759718067 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792030 | GGAAAATGGTGGGGG[A/G]AAAGAGAAAGAGAGA | 11060 |
rs759721883 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774598 | TTTTGCAGATACTCT[-/CA]GTTTCTTCCTTCAGC | 11060 |
rs759774700 | in-del | -/ACAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763644 | TTTCACAGGGAACAA[-/ACAG]ACTTACGAGAGACGA | 11060 |
rs759782275 | snp | A/G | 1.88606e-05 | 0.00307082 | missense | WWP2 | GRCh38.p7 | 16:69842098 | CAGCCCCCCAGCACA[A/G]ACTGCTTTGGTGGAA | 11060 |
rs759817643 | snp | C/G | 1.65321e-05 | 0.00287502 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929519 | CAGTGGGAGGATCCC[C/G]GGACCCAGGGGTAAG | 11060 |
rs759823632 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918453 | AAGTTTCATTGAAAC[A/G]TAAGAACACCCAGCA | 11060 |
rs759830592 | in-del | -/TC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918343 | TATTATCTGACACAT[-/TC]TCAGGGATGAAGGAT | 11060 |
rs759869076 | snp | A/G | 4.9703e-05 | 0.00498488 | intron-variant | WWP2 | GRCh38.p7 | 16:69938988 | AAAGTACTGGGCCCC[A/G]TGGGTTGCCTGACTG | 11060 |
rs759898935 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867054 | TTGGCCAGGCTGGTC[C/T]CGAACTCCTGACCTC | 11060 |
rs759912811 | in-del | -/TACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820825 | ATGAATACATGCATA[-/TACA]CACACACACACACAC | 11060 |
rs759931866 | in-del | -/TTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806935 | TTGCCCTAGATCTGT[-/TTTA]TTTATTTATTTATTT | 11060 |
rs759936464 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821654 | TTTCTACAGGTATAT[G/T]GTGACTGTTTGCATT | 11060 |
rs759942056 | snp | C/G | 1.66479e-05 | 0.00288508 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931775 | GAAGGGAGAGTGGCA[C/G]GCTGGCCCGATGCTC | 11060 |
rs759951093 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768483 | GGCGTGGTGGCAGAC[A/G]CCTGTAATCCCAGCT | 11060 |
rs759955815 | snp | A/C | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839910 | TATGAAATGTTTAGA[A/C]AGAGTGCAGCTTCCC | 11060 |
rs759961322 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930694 | ACAGAGTGAGTCCCT[A/G]TTTCTAAAAAATAAT | 11060 |
rs759966566 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866606 | TTAGCAGAATGTCCT[C/T]GAGGTTCATCCATGT | 11060 |
rs759999020 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917995 | AAAACAGCGTCTGGC[-/A]ACGTCAGTGCTCTGC | 11060 |
rs760012222 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840927 | TAGCTTCAAAGGGGT[A/G]CAATTTGAATTGCAA | 11060 |
rs760013393 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938729 | ATACCCATTAAGCAG[C/T]CACTCCCATATTTAG | 11060 |
rs760026164 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938893 | CTCAGGTTGGAGGCT[C/G]TCATCCCCTGGCCAA | 11060 |
rs760039269 | in-del | -/TTGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850810 | TTTTTGTTGGTGTTC[-/TTGT]TTGTTTGTTTGTTTT | 11060 |
rs760043812 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828139 | GCACTGGGACCCTGA[A/G]TCAAGAGAAATAAGG | 11060 |
rs760045066 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | WWP2 | GRCh38.p7 | 16:69888176 | GCCACACCGGCTGAA[A/G]GAGAGGAACCCAGCA | 11060 |
rs760052411 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912055 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 11060 |
rs760071247 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858328 | TCTTTGTGTCCCCAG[C/G]AGGACCTAGAATAGT | 11060 |
rs760098713 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902935 | GGAGGAGTGAGGTTC[C/T]GTGAGAAAGGGAGGC | 11060 |
rs760102604 | snp | A/G | 1.67464e-05 | 0.0028936 | intron-variant | WWP2 | GRCh38.p7 | 16:69936483 | CGGGGGCTCCGCTCC[A/G]GGGGTGGCGTGGAGA | 11060 |
rs760114400 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814578 | ATGCTGTCCATGTTC[-/TGT]GTGTGTTTCTTCTCT | 11060 |
rs760123301 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768384 | GAGGCCGAGGTGGGT[A/G]GATCACCTGAAGTCA | 11060 |
rs760137313 | snp | A/G | 1.6501e-05 | 0.00287232 | missense | WWP2 | GRCh38.p7 | 16:69799260 | GCACCGCATCTGTCA[A/G]CCTCTCCAACGTCTT | 11060 |
rs760141288 | snp | A/G | 4.97393e-05 | 0.0049867 | intron-variant | WWP2 | GRCh38.p7 | 16:69939436 | TGCTGGTTTTAGTGG[A/G]AGGTCGGGGGGCCTC | 11060 |
rs760190553 | snp | C/T | 1.65597e-05 | 0.00287743 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936447 | GAACAAGGAAGAGTA[C/T]ATCATGTGAGTCTCA | 11060 |
rs760206009 | in-del | -/GCAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897913 | CTCCATCTCAAAACA[-/GCAAA]ACAAAACAAAACAAA | 11060 |
rs760237007 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914703 | CGAGGCTGCAGTGAG[C/T]CATGATCATGCCACT | 11060 |
rs760237556 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837757 | GCACGCTTCCAATAG[C/T]GGTGTGTGTCCTGGA | 11060 |
rs760251113 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847721 | CCAGGCTCTTTTTAA[G/T]AACCCATTCTTGCAG | 11060 |
rs760255620 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909922 | GGCCTGTGGACAAAA[C/T]CCGGCCCTCTGACTG | 11060 |
rs760260072 | snp | C/T | 8.55132e-05 | 0.00653829 | intron-variant | WWP2 | GRCh38.p7 | 16:69799127 | TTTTCTTCTAAGTTA[C/T]AGGAATGATCTGCTT | 11060 |
rs760277750 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934369 | CATAGAGCTCGTAAC[C/G]TAAAAATGCAAGAAG | 11060 |
rs760290659 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839537 | CTGGGCCACTTCTCA[A/G]TTCTCTCTCCTTAAG | 11060 |
rs760292890 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761505 | ATGAACCGGCGAGAC[A/G]GAGGTTGCAGTCAGC | 11060 |
rs760303995 | snp | A/G | 0.000234913 | 0.0108352 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933173 | CACGGACAGGATACC[A/G]GGGCACCCTCTGCGT | 11060 |
rs760307529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883138 | AGTTTGGGTGGCAGG[A/G]TGAGACTCCATCTCA | 11060 |
rs760312095 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886846 | CTCCCTGTAAGAAAC[A/G]TTCACGAAGAATCTG | 11060 |
rs760313368 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817540 | CAGGTGTGAGCTACT[A/G]TGCCCAGCCAGATGC | 11060 |
rs760317996 | snp | C/T | 1.70956e-05 | 0.00292361 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933036 | CCGTGGTGACCTCCT[C/T]TCCAGGCTCTGCTTG | 11060 |
rs760345617 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923600 | GGTAGCTGATTTCCC[A/G]GGAGAACCCTGAACG | 11060 |
rs760352459 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799241 | TTGAGAAATGAACTG[C/T]TAGGCACCGCATCTG | 11060 |
rs760354678 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836453 | AGCATGTGGCATCAG[A/G]TTGCCTTGCTTTGCT | 11060 |
rs760365867 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896676 | AATAACAACAGTTAA[C/T]AAACACCCCCCCAGA | 11060 |
rs760374317 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804720 | TTCCTACTCCCCATG[C/T]CCCCTAAAAAATCTC | 11060 |
rs760382785 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763292 | CTTGACGAACTGTAA[A/C]TAGGTAGGGTGCCTG | 11060 |
rs760432405 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798525 | TTTTTGGTGTGTGTA[C/T]TCACATTTCTTTAAA | 11060 |
rs760437660 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858761 | TAAAGTCCGTGTACT[A/T]CAACTCTGCCAGAAA | 11060 |
rs760446080 | in-del | -/GAACAGTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934923 | ACGCTGCCTCCTGGT[-/GAACAGTA]GACTGGCTGGTGCAG | 11060 |
rs760449769 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906323 | GTGATCTGCCCGCCT[C/T]GGCCTCCCACAGTGC | 11060 |
rs760486697 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822358 | GAGCTAGAGGCTGGC[G/T]CTGAAGTGGTGAACA | 11060 |
rs760496429 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876571 | GTGTCATCATGTTGG[G/T]CAGGCTGGTCTCAAA | 11060 |
rs760528299 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891395 | TGCTATCTCTTAGGA[A/G]CTGCATCTTCTTGAG | 11060 |
rs760559744 | snp | A/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69941808 | CTCCGGGCCTCACAG[A/T]CCCTCCAGGCCTGGA | 11060 |
rs760571421 | snp | A/C | 4.98169e-05 | 0.00499059 | intron-variant | WWP2 | GRCh38.p7 | 16:69786974 | GATATTCTCTGAATT[A/C]TTTTTTCTGTTTGTC | 11060 |
rs760616827 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873169 | GGCTTTTCACGGAAG[-/TGT]TGTTGTGGCATTGTT | 11060 |
rs760625605 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763727 | CCTGCTAGATTGCAA[A/G]TCCTTCAAGGGCAGG | 11060 |
rs760658141 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881382 | AATAATATCTTCCTC[A/T]TAAGGGCATTGGGAG | 11060 |
rs760662119 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770655 | AGCACGGGTAAAACA[A/C]CCTGGAGCTTGCAAT | 11060 |
rs760670277 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941611 | CGTGTGTGTGCGTAC[A/G]TGTATATAACTGAAG | 11060 |
rs760679459 | snp | C/G | 4.94564e-05 | 0.0049725 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931256 | CTGGGGCTCCCGTGG[C/G]AGTTGGGGTTATTGA | 11060 |
rs760710036 | snp | C/T | 3.37593e-05 | 0.00410834 | missense | WWP2 | GRCh38.p7 | 16:69871877 | CCCGGTGCTCGGAGC[C/T]GGCACCGCCAGCCCG | 11060 |
rs760750206 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810452 | TTTTTTTGAGACGGA[A/G]TTTCGCTCTGTCCCC | 11060 |
rs760769343 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant | WWP2 | GRCh38.p7 | 16:69934145 | GTAAGGGGGCCCCAG[A/G]GGTCTGCCTAGTTCC | 11060 |
rs760779727 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843273 | AGAGTCCAAATATTA[C/T]ACTTGTTATACGTAT | 11060 |
rs760789476 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799729 | GTGTGCATGTGTGCA[C/T]GTGTGTGTCTGGGAT | 11060 |
rs760802949 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830864 | GTGGACTCCAGCCTG[C/T]GTGTGTCTGAGTTTC | 11060 |
rs760810777 | snp | C/G | | | missense | WWP2 | GRCh38.p7 | 16:69937141 | CTGACTGGCGTTTCA[C/G]CCGAGGCGTGGAAGA | 11060 |
rs760818159 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867483 | CGAGGCCAGGTGTCC[C/T]ATGACACCCAAGGCT | 11060 |
rs760840397 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861313 | GCTAAGCCCAACATA[C/T]GGCCTGGAAGTAGAT | 11060 |
rs760840562 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927245 | TGGGGCCGGCTCCCC[A/G]GGGCTCACCGAGAAT | 11060 |
rs760852496 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | WWP2 | GRCh38.p7 | 16:69841983 | ACACGAGTTGAGCTC[C/G]TCAATGCTTCTGTCT | 11060 |
rs760855581 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791567 | TTCTCTGTTGCTCAG[A/G]CTGGAATGTAGTGGC | 11060 |
rs760856909 | snp | C/G | 1.66051e-05 | 0.00288137 | intron-variant | WWP2 | GRCh38.p7 | 16:69938979 | CGTTCGGGCAAAGTA[C/G]TGGGCCCCGTGGGTT | 11060 |
rs760866264 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898867 | TGCCACCACTCCCAG[A/T]TACTTTTTCTGTATT | 11060 |
rs760869052 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921583 | TTTCCCAACTCCTAG[C/T]GTGCTAATGTTGCCC | 11060 |
rs760877696 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800326 | TTTCCCAAACCCTAG[C/G]CAGCCTTTTGTAATT | 11060 |
rs760890967 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818855 | CTTTCATTCACAAGC[A/G]CATCCAGCCTCCTTG | 11060 |
rs760947004 | snp | A/G | 4.96405e-05 | 0.00498175 | missense | WWP2 | GRCh38.p7 | 16:69937609 | AGAGCACCATCTACC[A/G]GCACTACACCAAGAA | 11060 |
rs760968567 | snp | C/T | 4.97781e-05 | 0.00498864 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931755 | TCCCGCCCCTGCCTG[C/T]TGTGGAAGGGAGAGT | 11060 |
rs760982037 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875996 | TTTTGCTCTTGTTGC[C/T]CAGGCTGGCATGCAG | 11060 |
rs760986974 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819736 | AGGCATGTAATTCAG[C/G]GATTTTAAAATGATT | 11060 |
rs761056397 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931554 | AGCGTTTCCAGGCAG[A/G]CGCTTTTCGAAGATT | 11060 |
rs761063633 | snp | A/G | 0.000164785 | 0.00907555 | missense | WWP2 | GRCh38.p7 | 16:69936363 | CTTCATCCAGGACAT[A/G]GAGATACTGGGCAAG | 11060 |
rs761070182 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885248 | ATAGTGTTTTTTTTA[A/C]AATTGAGTAAAATGT | 11060 |
rs761104178 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772252 | AGTCTGCTTGGGATT[A/G]GGAAGGGGCAACTGC | 11060 |
rs761130408 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786139 | TTTTTGGAGATGTCT[-/T]TTTTTTTTTTTTCTT | 11060 |
rs761149182 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | WWP2 | GRCh38.p7 | 16:69939416 | GAAGCCACACCTGGT[A/G]AGCCTGCTGGTTTTA | 11060 |
rs761152765 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808161 | TCAGCTTTGCCTAGT[A/G]TTGAATTTCATATTA | 11060 |
rs761165636 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903565 | CAAGGTCAGAAGATC[A/G]AGACCATCCTGGCCA | 11060 |
rs761169612 | snp | A/C | 4.37302e-05 | 0.00467581 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933136 | GTAGGTTACGTCATG[A/C]TGTTCTACCACAGGG | 11060 |
rs761171650 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797209 | CTTGCTGGTCCCAAA[C/T]GAACATCAGAATTGT | 11060 |
rs761178572 | in-del | -/TGATTCAACGTGATTTG | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923967 | GATTTTTTTCAGTAA[-/TGATTCAACGTGATTTG]TGATGGAGAATTTTA | 11060 |
rs761188734 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69838355 | AGTGCCTGACCACAC[C/T]CCCTCTTAATCCACG | 11060 |
rs761199975 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931952 | GGCTACAGCATCAAT[C/G]GCCAGAAAGCTGCCT | 11060 |
rs761211622 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923404 | GAAAGAGAGCCAACA[C/T]TGCATGAAGGCTGAG | 11060 |
rs761222411 | snp | C/T | 4.5044e-05 | 0.00474552 | intron-variant | WWP2 | GRCh38.p7 | 16:69939819 | CCTAGGGCTGACTGT[C/T]GTGCTTCCCCACTCT | 11060 |
rs761261074 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826429 | ACAAAAAAATTAGCC[A/G]GGCGTGATGGTGGGT | 11060 |
rs761265157 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849920 | TTTATTGCATAGATA[-/T]TTATTTGGCATTTAC | 11060 |
rs761272774 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868138 | AACTCCAGATTTAGG[G/T]CAAGGGGAGAATCTG | 11060 |
rs761278022 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814266 | CCTGGGCTCAAGCGA[A/T]CCTCTTGCCTCAGCC | 11060 |
rs761278798 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839829 | CCCTATGCTTTTCTC[A/G]CAGTCCTGCAAGTAT | 11060 |
rs761299618 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856633 | ACAAAAATTAGCTGG[G/T]TGTGGTGGCATGTGC | 11060 |
rs761311112 | snp | C/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940603 | AACAGCAAACTCCCT[C/G]AGACTTTGTCCATGT | 11060 |
rs761316377 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804592 | TATTGTAAAATTATG[-/T]TTTAATATCTGGCAG | 11060 |
rs761330365 | snp | A/C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912213 | AGAATTGTTTGAACC[A/C/G]CAGCGGCGGAGGTTA | 11060 |
rs761338131 | in-del | -/TTTA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866271 | AAAAAGGTTTCACAT[-/TTTA]TTTATTTATTTATTT | 11060 |
rs761354117 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785455 | ATTGCATAATGAAAT[A/G]TGTCAACATTTGGAA | 11060 |
rs761381403 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767690 | GGGGGCTATGTGGGG[-/A]TTGATGCATCTGAGG | 11060 |
rs761390529 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878820 | AAATACCTGTATATA[A/G]CTTTGTTTCTTGAGT | 11060 |
rs761399815 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939567 | GGGGCTGTGATGGGC[A/G]TCTGATCTACCGGGT | 11060 |
rs761414227 | snp | A/T | 3.30066e-05 | 0.00406229 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929478 | ATGGACGGGTGTATT[A/T]CGTGAACCATAACAC | 11060 |
rs761416743 | snp | A/G | 1.73495e-05 | 0.00294524 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931937 | TACCCCGCTTCCCCA[A/G]GCTACAGCATCAATG | 11060 |
rs761444505 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787088 | TTTGAAAGGTGAGTG[A/G]CACTGTATAATGTCT | 11060 |
rs761460019 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887792 | ATGTTAGAAAAACTT[C/G]ATAAAGTTATGTAAA | 11060 |
rs761461353 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839893 | TGGTGCTGACCCAGT[A/G]ATATGAAATGTTTAG | 11060 |
rs761500926 | snp | A/C | 1.65348e-05 | 0.00287526 | missense | WWP2 | GRCh38.p7 | 16:69799214 | GATTTAAAGGTCTGG[A/C]GCTGCCATACCTTGA | 11060 |
rs761502608 | snp | A/C/T | 3.30258e-05 | 0.0040635 | missense | WWP2 | GRCh38.p7 | 16:69937198 | TCAACGAGGTGGCCC[A/C/T]GCTGGAGTGGCTGCG | 11060 |
rs761515481 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763159 | CAGCGTTACCTCAGC[A/C]ACATAGTGACTGCTG | 11060 |
rs761517582 | in-del | -/ATG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887294 | GCCTCTTTAGTGTGT[-/ATG]ATGAGCTTTTTGAAA | 11060 |
rs761519005 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888358 | TGGCTAGTAGCCTCT[A/G]GGGAGGCTGCTGTGC | 11060 |
rs761534873 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792306 | AAACAAGAAACAAGC[C/T]GTTTGGAACTTATTG | 11060 |
rs761549561 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845222 | TCAGTCAGAGGGCCT[C/T]ACACAACGGGAGCAC | 11060 |
rs761550151 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931160 | TTCCTAGGACGAAGC[A/G]AGGTTCCCCTGGTGC | 11060 |
rs761567700 | snp | A/G | 1.66863e-05 | 0.0028884 | intron-variant | WWP2 | GRCh38.p7 | 16:69798875 | GCAAGATGGGGAAAG[A/G]GAGAGGGTGCTCCGA | 11060 |
rs761570637 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834699 | ACCCAGCTCATGTTT[C/T]GTATTTTTAGTAGAG | 11060 |
rs761598926 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863820 | AAATGGAAATGTACA[C/T]GTATAGCCTTTGGTG | 11060 |
rs761599715 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915096 | TGAGGGAGAGATGTG[A/G]CCGAGAGAGGAAGGC | 11060 |
rs761606433 | snp | C/T | 1.9856e-05 | 0.00315081 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939948 | AGGAGTAACCGAGGC[C/T]GCCCCTCCCACGCCC | 11060 |
rs761615562 | snp | A/G | 4.94711e-05 | 0.00497324 | missense | WWP2 | GRCh38.p7 | 16:69917791 | TGGCAGCGTCCGACC[A/G]CGGAGTACGTGCGCA | 11060 |
rs761638554 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897542 | GGGACATGCATTTAA[A/G]CTGCTATACGGTGTT | 11060 |
rs761638948 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793310 | TGAGTCAAGATTGCA[C/T]CACTGCACTCCAGCC | 11060 |
rs761641434 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833871 | AGATCAGTGGCCCTG[C/T]GGGGCCTGGCTGATG | 11060 |
rs761685858 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933764 | TCAAATGCAGTTGCC[A/G]CCCTGGTTCACTGTA | 11060 |
rs761707200 | snp | A/C | 2.00696e-05 | 0.00316771 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842118 | CTTTGGTGGAAGATC[A/C]CGGTAAGACCCCCCT | 11060 |
rs761760910 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821561 | GAAGTCGGTCAGCCT[C/T]GTGGGAACACATATT | 11060 |
rs761762252 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821167 | AGCCCTCTGTGTGTC[A/G]CTTTCTATCATCCTG | 11060 |
rs761794916 | snp | C/T | 1.6516e-05 | 0.00287362 | missense | WWP2 | GRCh38.p7 | 16:69930255 | GCCCGGGGTTTGAGT[C/T]GGGGTAAGGACTTTG | 11060 |
rs761807681 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916392 | TTTTTGTAGAGATGG[A/G]GGTCTCCCTCTGTTG | 11060 |
rs761831231 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882112 | GGCATGAGCCACCGC[A/G]CCCAGCCTAAGTTTT | 11060 |
rs761843600 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864996 | AGAACTTATGATGTT[A/G]AGCATCTTTTTTTGT | 11060 |
rs761850047 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929432 | CTGATGTTCTTTCTT[C/T]CTTCTCATGTGGCAG | 11060 |
rs761861977 | snp | C/G | 6.73163e-05 | 0.00580117 | intron-variant | WWP2 | GRCh38.p7 | 16:69917891 | TCTACCAGGTGAGAG[C/G]GCAGGCGCTTGGCCC | 11060 |
rs761917086 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891440 | TTATCTTTTATGAGG[A/C]TATATAAATGCAGCA | 11060 |
rs761932903 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810135 | CCACGGACAGAATTC[G/T]TTCTTTCATTTGCTC | 11060 |
rs761964440 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929746 | TCCTGGTGGATGGAG[A/G]GCGGCCCGGCTGGCG | 11060 |
rs761966620 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900980 | TTAGTGTGCTTAGAT[A/T]TAAAGGCTAGTTCCT | 11060 |
rs761980829 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769477 | GAAATAAAATATTGA[G/T]ACTGGTGTGTAATTT | 11060 |
rs761982399 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938302 | TACAGGCGTGAGCCA[C/T]TGTGCCCAACCCATT | 11060 |
rs761993448 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | WWP2 | GRCh38.p7 | 16:69908810 | TATTATGTTGACCAC[A/G]ATACCAAGACCACCA | 11060 |
rs762001544 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869340 | TTGCTACGTTTCTCC[C/T]TTTTTCTCCTTTTTT | 11060 |
rs762006861 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890917 | TCCTTGGGGCATTTA[G/T]AACGTGATGAGGGCC | 11060 |
rs762013915 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789899 | AACTTTTGACTCCCC[C/T]AAAACTTTACTAATA | 11060 |
rs762022820 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811808 | AATAGAACAAAGAAC[C/T]CCTCAATGTCGTCCT | 11060 |
rs762031310 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794903 | ATTAGGTACTGAATT[C/G]GGGGAAAAATGGCTT | 11060 |
rs762039376 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830164 | TTCACCACATTGCCT[A/G]GGTGGGTCTTGAACT | 11060 |
rs762040586 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817902 | TGCCCAGCCTAAATT[A/C]TTGTAAAGATACCTT | 11060 |
rs762064474 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870907 | GTCTGATAGGTTTTC[-/T]GCTGCTAAATTCCAC | 11060 |
rs762083655 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928995 | GGACCACGCCCTGTA[A/G]GACAGAGGCGCCCAG | 11060 |
rs762144190 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883881 | TCAGATCCGAGTAGT[A/G]TTGATTGGAGGGTCT | 11060 |
rs762164829 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | WWP2 | GRCh38.p7 | 16:69840182 | AAAGGCAGCGTTGTC[C/T]CAGGCGGAGAGCTGA | 11060 |
rs762183783 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917644 | TAGGCATCCTGAGAC[-/TT]TTCTAGAATTGGGGG | 11060 |
rs762197919 | snp | C/T | 4.58684e-05 | 0.00478875 | intron-variant | WWP2 | GRCh38.p7 | 16:69939173 | GCAGTGCGGACAGCT[C/T]AGAGGGAGGGGGAAA | 11060 |
rs762202302 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935013 | GCGTCTGTATTTAAC[A/T]GGAAAGAGGGACACA | 11060 |
rs762222295 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885612 | GTTATTATAATCTTC[A/G]GTTGAATTAGAGGAT | 11060 |
rs762226818 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877159 | GCTCTTTCGTCAACA[C/T]TGAAAAGCTGTTGTT | 11060 |
rs762251119 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849982 | CCAGATGTGGCATGC[A/G]CCAGAAAGCTGGTTA | 11060 |
rs762252673 | snp | A/G | 1.67959e-05 | 0.00289787 | intron-variant | WWP2 | GRCh38.p7 | 16:69840302 | GACTGTGCCGGGACA[A/G]GGTGGGGCTGGGCGG | 11060 |
rs762284896 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818752 | ACTCTCATTCAGTCT[C/G]CCTTGCTCGTTTTTC | 11060 |
rs762289415 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778265 | TTGACTTTCCCATCC[C/T]CCTCCCAATAAGTCC | 11060 |
rs762289439 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764860 | ACGATCATATAATGT[A/G]TAAACATGTATGATA | 11060 |
rs762308324 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894911 | TGGTTTCTTACATAA[C/T]GGAGGGCGTTGTGTT | 11060 |
rs762310233 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807842 | TGCACACCTGTAGTC[C/G]CAGCTACTTGAGAGG | 11060 |
rs762313244 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849047 | AAAGATCTGTAATCT[C/T]GGAGACTTATAAAGC | 11060 |
rs762320041 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832397 | TTAGTGTATTTCTCT[-/A]AAAGATAAGAACTCT | 11060 |
rs762334892 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870144 | GCTTATCTGTAAAGC[A/G]GGGATAATAATATTA | 11060 |
rs762360961 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766040 | GCCTGTCTCGAGACT[A/T]CTAGATCTAATTGCC | 11060 |
rs762373705 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941596 | TCATGTGTGTTCGTG[C/T]GTGTGTGTGCGTACG | 11060 |
rs762381932 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant | WWP2 | GRCh38.p7 | 16:69925492 | TGGCTGGGGTAAGTA[C/T]TGAGTTCTCTTCCTG | 11060 |
rs762402210 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853632 | GCTGAGACCAGACTC[-/AG]GGACTGACGAAGAGG | 11060 |
rs762407550 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836966 | CTCATTTTGGTTGCT[G/T]AGGTTGGAGTGCCCT | 11060 |
rs762455321 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855451 | AACATTTTGTGCCTT[G/T]GTTTCTATAATAATG | 11060 |
rs762461461 | in-del | -/ACGTGCGCA | 1.64914e-05 | 0.00287149 | cds-indel | WWP2 | GRCh38.p7 | 16:69917798 | GTCCGACCGCGGAGT[-/ACGTGCGCA]ACTATGAGCAGTGGC | 11060 |
rs762466124 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920228 | TTCCTTAGCAGAGGT[A/G]AGCAGAAAGTGTGGT | 11060 |
rs762466287 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932539 | TCTGTACTTTAACAA[C/T]CAGGCCAGCAGCATC | 11060 |
rs762470106 | snp | C/T | 1.69913e-05 | 0.00291468 | intron-variant | WWP2 | GRCh38.p7 | 16:69929416 | CTCTCCGTGTTTGAA[C/T]CTGATGTTCTTTCTT | 11060 |
rs762479272 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904920 | GAAGCTGTCTCCATA[C/T]TTCCAGTTCTTACAT | 11060 |
rs762484352 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771351 | CTCCCGGGTTCAAGC[C/T]ATTCTCTTGCCTCAG | 11060 |
rs762488499 | snp | A/G | 4.96635e-05 | 0.0049829 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931854 | TCTACATCATCATGC[A/G]TGGCGAGGAGGGCCT | 11060 |
rs762490716 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795779 | CAGCCTCCTGAGTAG[C/G]TGGGACTACTGTTGT | 11060 |
rs762493059 | in-del | -/GACTCATCTTT | 1.66682e-05 | 0.00288684 | intron-variant | WWP2 | GRCh38.p7 | 16:69798646 | ATCTGGGAGCCCTGG[-/GACTCATCTTT]GACTTTTTCTTTCTT | 11060 |
rs762512033 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825994 | AGAAGCAGCCAGGCG[C/T]GGTGGCTCATGCCTG | 11060 |
rs762516294 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793561 | GTTGGGGATGAGATT[-/A]TAGAGGTGTGGAAAA | 11060 |
rs762555951 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932057 | TGAACCCGCCAGGCG[C/T]GGTGGCTCACGCCTA | 11060 |
rs762571504 | snp | A/G | 1.90991e-05 | 0.00309018 | intron-variant | WWP2 | GRCh38.p7 | 16:69939836 | TGCTTCCCCACTCTC[A/G]ATAGCTTCAACCGTC | 11060 |
rs762574554 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914757 | CAAGACCCTGTCTCA[A/G]AGAAACAAAAAAGAA | 11060 |
rs762575973 | snp | A/G/T | 3.35645e-05 | 0.0040965 | intron-variant | WWP2 | GRCh38.p7 | 16:69936489 | CTCCGCTCCAGGGGT[A/G/T]GCGTGGAGATCTAGT | 11060 |
rs762597985 | snp | G/T | 1.65026e-05 | 0.00287246 | missense | WWP2 | GRCh38.p7 | 16:69930249 | ATCCTCGCCCGGGGT[G/T]TGAGTCGGGGTAAGG | 11060 |
rs762601279 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827712 | GCTGCGGTTCCCTGA[A/G]GGCACAGAGCATGGG | 11060 |
rs762634781 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857810 | GAGACTACAGGTGTG[C/T]GCCACCATGCCTGGC | 11060 |
rs762638597 | snp | A/G | 3.64179e-05 | 0.00426704 | missense | WWP2 | GRCh38.p7 | 16:69939933 | CCGAGGGCTTTGGAC[A/G]GGAGTAACCGAGGCC | 11060 |
rs762649177 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69857865 | TGACAGTGTCTTCCT[G/T]TGTTGCCTAGTCTGG | 11060 |
rs762653214 | snp | A/G | 3.29468e-05 | 0.00405861 | missense | WWP2 | GRCh38.p7 | 16:69888071 | ACAGCCACTGATCCC[A/G]AAGAACCTTCCGTTG | 11060 |
rs762663557 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890591 | GGAGAGAAAATGGCC[A/G]CCTGTGTCCCCAGTG | 11060 |
rs762668001 | snp | C/T | 3.33034e-05 | 0.00408051 | intron-variant | WWP2 | GRCh38.p7 | 16:69936465 | CATGTGAGTCTCAGG[C/T]GCCGGGGGCTCCGCT | 11060 |
rs762668154 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785146 | GCTGAGGCACGAGAA[G/T]CACTTCAACTTGGGA | 11060 |
rs762689777 | snp | A/C | 1.6504e-05 | 0.00287258 | intron-variant | WWP2 | GRCh38.p7 | 16:69934139 | GCCATGGTAAGGGGG[A/C]CCCAGGGGTCTGCCT | 11060 |
rs762692298 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802518 | TACAGTATTTGTCCT[G/T]TTATGACTGGCTTAT | 11060 |
rs762714131 | snp | C/T | 1.65463e-05 | 0.00287626 | intron-variant | WWP2 | GRCh38.p7 | 16:69871981 | AGCTGTGGGCTCTCA[C/T]CCGTTCTAACGTGGA | 11060 |
rs762728340 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772370 | TCTGCCCTTACTTTC[A/G]GAGGTACCTGTACTA | 11060 |
rs762732099 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826572 | GTGAGACTCCGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAGTGGAG | 11060 |
rs762743326 | snp | A/G | 1.66316e-05 | 0.00288367 | intron-variant | WWP2 | GRCh38.p7 | 16:69798857 | CCCTTCTTTTTGAAC[A/G]CAGCAAGATGGGGAA | 11060 |
rs762773918 | snp | C/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761237 | TTGAAGCTGGGAGTT[C/G]GAGCCCAGCCAAAGC | 11060 |
rs762818192 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844288 | GCACCTGGAACTGGA[A/G]GAAACAATTTCTTAA | 11060 |
rs762819561 | in-del | -/TTTGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817249 | CAGTAATGGGTGTGC[-/TTTGT]TTTGTTTTGTTTTTT | 11060 |
rs762822439 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938180 | ACAATTAACTATTAA[-/T]TTTTTTTTTTTTCAA | 11060 |
rs762854830 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801197 | AAAAAAAAAAAAAAA[-/G]GCAATTTTACTTTAA | 11060 |
rs762879249 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898478 | TCCTGCTAAAACTTA[A/G]TGTTGTCAGGTTCGT | 11060 |
rs762905609 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832288 | AGTAGCCATCTATGA[C/T]GGGCCATTCCTGTCT | 11060 |
rs762909935 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844971 | TGCTGTTGCAGGTAT[A/G]AAGGTCACTGTGCAC | 11060 |
rs762925299 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | WWP2 | GRCh38.p7 | 16:69934038 | TTGAATATGCCGGAA[A/G]GAACAATTACTGCCT | 11060 |
rs762946298 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780539 | TACGCGTCTTTAACT[C/T]TGCCGGAGGTTGTCA | 11060 |
rs762964811 | snp | C/G | 1.77741e-05 | 0.00298107 | intron-variant | WWP2 | GRCh38.p7 | 16:69937699 | ATTTGGGCCATCAAC[C/G]AAAGGAAACGGGTCC | 11060 |
rs762976959 | snp | A/G | 1.69527e-05 | 0.00291137 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931463 | ACAGGAGAACAGATG[A/G]CCACTTGAGGCTCGA | 11060 |
rs763006269 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863726 | CCCTTTGTAGCCAGC[C/T]CCTCCTTGTACCCGT | 11060 |
rs763006367 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851607 | TTTATTCATTCATTT[A/T]CTGGTTGCTTCCAAG | 11060 |
rs763010039 | in-del | -/ATAATG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776536 | GAAGTTTCTTAACTT[-/ATAATG]ATAATAGGCCGGGCG | 11060 |
rs763033318 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931530 | GCCCTACCTAGCCAC[A/G]TGAAGATCAGCGTTT | 11060 |
rs763034598 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796623 | CTGTAAAGTCAAACG[C/T]CCTAAGTAATGCACC | 11060 |
rs763041788 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883978 | ATTTTTAATAGTTAT[A/G]TGTTACTAAAACTTT | 11060 |
rs763052311 | snp | C/T | 1.65438e-05 | 0.00287605 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937601 | CTGGCAGAAGAGCAC[C/T]ATCTACCGGCACTAC | 11060 |
rs763058987 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917387 | TCCTAGATTTGCTAG[C/T]AGATGTCCTGAGATT | 11060 |
rs763079446 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892528 | TCTTACCCTTTCCCA[A/G]TCTATTTTAACTTTT | 11060 |
rs763084660 | snp | C/T | 1.69137e-05 | 0.00290802 | intron-variant | WWP2 | GRCh38.p7 | 16:69871779 | AGTGACTTATGTCTG[C/T]CTGCTTTCTACTTTG | 11060 |
rs763102130 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840981 | TCAGTGGCCGGATGG[G/T]CCTTGACTGTGGAGA | 11060 |
rs763131363 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930635 | GCTCAGGAGTTTGAG[A/G]CTGCAGTGAGCTATG | 11060 |
rs763144507 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780970 | GAGGTCAAGGTTGTA[A/G]TGAGCTATGATCATG | 11060 |
rs763158843 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767734 | AATCATTTCTCAGAA[C/T]GACTGTCCATGGCTT | 11060 |
rs763166177 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775202 | TCTCTGTGTCCTTTT[C/G]TTTTCAGAGAAGGAT | 11060 |
rs763220326 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929763 | CGGCCCGGCTGGCGG[A/G]TGTTGCTGGTCTCCA | 11060 |
rs763271343 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863581 | TGGGGGCAGAGGTTG[C/T]AGTGAGCCGAGATTG | 11060 |
rs763311987 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938467 | TACTAACAATATAAA[A/G]AATTAGCCAGGCATG | 11060 |
rs763312169 | snp | C/G | 5.39428e-05 | 0.00519312 | intron-variant | WWP2 | GRCh38.p7 | 16:69888259 | TGCTGGGTGAGTAGT[C/G]TTCTGTCCCATAACA | 11060 |
rs763318720 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891627 | CAGACTGTTTCATGA[C/T]GCGTGCCCTGGTCAC | 11060 |
rs763322178 | snp | A/G | 3.24396e-05 | 0.00402725 | missense | WWP2 | GRCh38.p7 | 16:69939102 | TGCCGCCTGCCCGTC[A/G]GGGGATTTGCCGAAC | 11060 |
rs763338574 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789094 | ACAGAGTCTCGCTCT[A/G]TCGCCCAGGCTGGAC | 11060 |
rs763368253 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877376 | CATAGAATTGAAGAG[C/G]GTTCGGGTCTTGCTC | 11060 |
rs763400618 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860179 | AAAAATTAGCCAGGC[G/T]TGGTGGTCCGATTCC | 11060 |
rs763403135 | snp | A/C/G | 8.30136e-05 | 0.00644211 | intron-variant | WWP2 | GRCh38.p7 | 16:69937505 | GAGTGGACGATGCGC[A/C/G]GGGAGGGACCTGCCG | 11060 |
rs763403496 | snp | A/G | 3.29783e-05 | 0.00406055 | intron-variant | WWP2 | GRCh38.p7 | 16:69840085 | CTTAACTTGGGGTGC[A/G]TTCTCTTTAGCCCAT | 11060 |
rs763424001 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789694 | CTTCTAGCAATGTGC[A/G]AGAGTGCCTGTTTCC | 11060 |
rs763426856 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877929 | TCTCCTGCCTCAGCC[C/G]CCCCAGTAGCTGGGA | 11060 |
rs763429151 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829881 | ATGTTACTTGAACCT[C/T]CTGGGTTCAAGTAAT | 11060 |
rs763442752 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69910962 | TCCTGAGTTTTAGGT[A/C]AAGAACTTTGAGCCT | 11060 |
rs763448196 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887342 | CTAGCAAACAAATGA[C/T]AAATTTAAAGAAAAG | 11060 |
rs763479470 | in-del | -/GTATACATATACACAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816753 | TATACATATACACAC[-/GTATACATATACACAT]ACACACATACACATA | 11060 |
rs763492399 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775965 | AGTGTCCTTGTTTCT[A/G]TCTCCCCTGTTATCT | 11060 |
rs763493082 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | WWP2 | GRCh38.p7 | 16:69840165 | ACCTGCAGACGGAGA[A/G]CAAAGGCAGCGTTGT | 11060 |
rs763508332 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807802 | TACAAAAAAGAAATT[A/T]AAAAAAATTAGCCAG | 11060 |
rs763543297 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847888 | TGAATTTTGGTGGGG[A/T]CAAACTGCATCCAAA | 11060 |
rs763561480 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810018 | AAGTGGGTCACAGTG[C/T]GGTTAGGTAACTCCT | 11060 |
rs763563273 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817818 | CTTGTGTCACCATGC[A/T]TGGCTAATTTTGGCA | 11060 |
rs763574191 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763595 | TAGTTTTTGCAGCAG[C/T]GCCTATGAGTGAGGT | 11060 |
rs763608723 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839616 | TTTTTTTCCTTATTT[C/T]AAGACAATACATTTT | 11060 |
rs763618268 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887547 | ACTAGCTGGGATTAT[A/C]GGTGTGCGCCACCAT | 11060 |
rs763622504 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856485 | AAAATCATTAAAAGA[C/G]CCATTTGGTGGCCAG | 11060 |
rs763630668 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69910270 | CAGTATTTTGTTTAT[A/G]TTATCAAATACCCAG | 11060 |
rs763631312 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938820 | CCCAGAGATGTCCCA[C/T]GGACTGGTGGGAATC | 11060 |
rs763644681 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815258 | TCAGGCCATCTTGGC[C/T]TCCCAAAGTGCTGGG | 11060 |
rs763648511 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | WWP2 | GRCh38.p7 | 16:69925499 | GGTAAGTACTGAGTT[C/T]TCTTCCTGGCCCTTG | 11060 |
rs763662795 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784168 | GCAGTGGCATGATCT[C/T]GGCGCACTGCAACCT | 11060 |
rs763671638 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772561 | GCTATAGGCAGTGTG[A/T]CCCTAGTAGCAGCTC | 11060 |
rs763676700 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813578 | AGCGATCCCCCCACC[C/T]CAGCCTCCAGAGTAG | 11060 |
rs763685380 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902391 | TAGGGAAAGGAAAAA[A/G]TACCTAAGATTAATT | 11060 |
rs763693568 | snp | A/G | 1.65597e-05 | 0.00287743 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931859 | ATCATCATGCGTGGC[A/G]AGGAGGGCCTGGACT | 11060 |
rs763697852 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817416 | ACCATGCTCAGCTAA[C/T]TTTTGTATTTTTAGT | 11060 |
rs763698650 | snp | A/G | 1.75437e-05 | 0.00296168 | missense | WWP2 | GRCh38.p7 | 16:69871908 | TCAAGAACTCAGGCC[A/G]CAGTGGCTTGGCCAA | 11060 |
rs763706228 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896685 | AGTTAACAAACACCC[C/G]CCCAGAGCTGACCAT | 11060 |
rs763732833 | snp | A/C | 1.64868e-05 | 0.00287109 | missense | WWP2 | GRCh38.p7 | 16:69798771 | CTCCCCAGTGAGACC[A/C]AGAAGACTGGGAAGC | 11060 |
rs763735462 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924881 | CCCAGATGGGAGGTT[C/G]GGGGGGACGCCGAGG | 11060 |
rs763750993 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785181 | GAGGCTGCAGTGAGC[C/T]GAGATTGTGCTACTG | 11060 |
rs763751216 | in-del | -/T | 0.000411814 | 0.0143436 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931145 | TGAACATCTTTGCTC[-/T]TCCTAGGACGAAGCA | 11060 |
rs763763470 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775566 | TCATGTGTTGTCTGC[C/T]GTTTCCATTAGAGCC | 11060 |
rs763773885 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791454 | GCTGGTCTCAAACTC[C/G]TGACCTCAGGTGATC | 11060 |
rs763786417 | snp | C/T | 1.65677e-05 | 0.00287812 | intron-variant | WWP2 | GRCh38.p7 | 16:69798678 | TTCTTTCTTTCTCTC[C/T]CAGTGGTGTCCGCAA | 11060 |
rs763805967 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843650 | AAGTGGGAGGATCGC[C/T]TGAGGCCAGGAGTTC | 11060 |
rs763813695 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851495 | TTTACGTTTCTTTCA[C/T]GTCTTCTCATGGCTT | 11060 |
rs763842398 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69933718 | ACATCACCTGGGAGC[C/T]GACAATCACACGTTT | 11060 |
rs763854389 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802555 | CAGCATAATGTCCTC[A/G]AGGCTTATTCATGTT | 11060 |
rs763908610 | in-del | -/CACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883401 | TTCTAAGAATGTGCG[-/CACACACA]CACACACACACACAC | 11060 |
rs763930833 | snp | A/G | 1.79806e-05 | 0.00299833 | missense | WWP2 | GRCh38.p7 | 16:69939846 | CTCTCAATAGCTTCA[A/G]CCGTCTGGATCTTCC | 11060 |
rs763933071 | in-del | -/A | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940083 | TCTCGCTGCTGGCAG[-/A]AAAAGCCTGATCCCA | 11060 |
rs763940130 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926594 | TATACCTGCAGGGTA[C/T]CACTTAGTCAATGAG | 11060 |
rs763970660 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905153 | CTCACACTGCTTGGC[A/T]GCGCTCTCTGAGCCT | 11060 |
rs763971615 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871556 | TGTAGGGGCAATTCA[C/T]TCTGGATTTGTTTAC | 11060 |
rs763978892 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | WWP2 | GRCh38.p7 | 16:69934044 | ATGCCGGAAAGAACA[A/G]TTACTGCCTGCAGAT | 11060 |
rs763996918 | in-del | -/AAAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765212 | TCTCAAAAAAAAGAA[-/AAAG]AAAAAGAAAAAAAGT | 11060 |
rs764003516 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863736 | CCAGCTCCTCCTTGT[A/T]CCCGTCGCTGCTGGC | 11060 |
rs764012419 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792269 | CACTGAAAAACTGAT[A/C]TCTGAAAAGCATAGT | 11060 |
rs764042927 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | WWP2 | GRCh38.p7 | 16:69934140 | CCATGGTAAGGGGGC[C/T]CCAGGGGTCTGCCTA | 11060 |
rs764054382 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928697 | GGAGGATCACTTGAG[A/G]CCAGGAGTTCGAGAC | 11060 |
rs764063915 | in-del | -/CTCTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817657 | GCACTTTTTGTTAAA[-/CTCTTTTTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs764068042 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905934 | ATGGTGATTCCACCT[G/T]AAAGGATGAAGGCAA | 11060 |
rs764076465 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833800 | CTCTAGCCATGCTCT[A/G]AATTGGCACTGTTTG | 11060 |
rs764078463 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819991 | ATGCCTGTGATCTCA[C/G]TGCATTAAGAGGCTG | 11060 |
rs764085461 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851732 | ATGCCTGTAATCCTA[G/T]CACTGTGGGAGGCCG | 11060 |
rs764086074 | snp | C/T | 1.68701e-05 | 0.00290427 | intron-variant | WWP2 | GRCh38.p7 | 16:69917690 | GTCATTATATTCATT[C/T]TGAGGTTCCTATTTC | 11060 |
rs764128154 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808415 | TTTTATTTTTATTTT[G/T]TTTGAGATGGAGTTT | 11060 |
rs764152847 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797479 | TGGGGTGATGATATA[C/T]TCCCTGCCTCATGGG | 11060 |
rs764156333 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916113 | TGAGAAAGCTAGGAA[A/G]GTTCCAGATTTTTGT | 11060 |
rs764157107 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855330 | TTAAGTATTTTTTAG[-/T]TCACTTCAGTCTGCC | 11060 |
rs764167612 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890865 | TCCTGCCAGAGGCTG[A/C]AACACGTTTCTGAGG | 11060 |
rs764223455 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767773 | CTGAGGCCCCTTCCT[C/T]GTTGTTGCTTACTTA | 11060 |
rs764226847 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940685 | TGTCACTTTCTGTCC[A/G]GGAGCTGGCACCCCA | 11060 |
rs764240388 | in-del | -/GCG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776814 | GCCTGGGCAACAAGA[-/GCG]AAATTCCATCTCGAA | 11060 |
rs764247840 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915107 | TGTGGCCGAGAGAGG[A/G]AGGCCACTGCCAGGC | 11060 |
rs764255802 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900395 | CACTTTTGGGAGGCC[A/G]AAGCAGGAAGATTGC | 11060 |
rs764294633 | snp | C/T | 1.64909e-05 | 0.00287144 | missense | WWP2 | GRCh38.p7 | 16:69888194 | GAGGAACCCAGCACT[C/T]CGGGTACACAGCAGC | 11060 |
rs764322997 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787885 | AGCGTATCTGGTTGA[C/T]TCGATCTTCAAAATG | 11060 |
rs764326532 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826853 | CTGAGGCAGGAGAAT[A/G]GTGTGAACCCGGTAG | 11060 |
rs764334372 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841038 | GTTTGGGGTGCTTTG[A/G]TGCTTGGAGAAAAAC | 11060 |
rs764339705 | snp | C/T | 1.68371e-05 | 0.00290143 | intron-variant | WWP2 | GRCh38.p7 | 16:69936030 | CGCTGATAGGAGGGA[C/T]GTCTCTGGGTGGGAA | 11060 |
rs764355965 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812297 | TAGCCTCCTGAGTAG[A/C]TGGGATTACAGGCAC | 11060 |
rs764387748 | snp | C/T | 3.35419e-05 | 0.00409509 | intron-variant | WWP2 | GRCh38.p7 | 16:69936488 | GCTCCGCTCCAGGGG[C/T]GGCGTGGAGATCTAG | 11060 |
rs764410848 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789097 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGACTGC | 11060 |
rs764431749 | snp | C/T | 1.65378e-05 | 0.00287552 | missense | WWP2 | GRCh38.p7 | 16:69935892 | GACACGGGCTTCACC[C/T]TCCCTTTCTACAAGC | 11060 |
rs764432427 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789751 | CAGACTTTTAACTTT[A/T]GCCTGTTTCATTGGT | 11060 |
rs764433497 | snp | A/G | 4.62995e-05 | 0.0048112 | intron-variant | WWP2 | GRCh38.p7 | 16:69939165 | CCTGGCTGGCAGTGC[A/G]GACAGCTCAGAGGGA | 11060 |
rs764437368 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920101 | CACCCAGCTGATGGA[C/T]CCCCGACTTTTAATC | 11060 |
rs764447216 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817881 | GATTACAGGTGTGAG[C/T]CATTGTGCCCAGCCT | 11060 |
rs764519328 | snp | A/G/T | 6.53429e-05 | 0.00571559 | missense | WWP2 | GRCh38.p7 | 16:69939106 | GCCTGCCCGTCGGGG[A/G/T]ATTTGCCGAACTCAT | 11060 |
rs764525220 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763614 | TATGAGTGAGGTTGG[C/G]AAGATGTATTCTCAT | 11060 |
rs764567108 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874836 | AAGGCCCAGTGACTC[A/G]CTAGGTCTTAGTTTT | 11060 |
rs764622024 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933474 | TACATTGTCATGGAT[C/T]GGGGTTGGAAATGTG | 11060 |
rs764639858 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835387 | TATTATAGGGTTCCT[C/T]TGGCTCAATTTTTTT | 11060 |
rs764640725 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803728 | GCCTAGCCAATATGG[C/T]GAGACCCTGTCTCTA | 11060 |
rs764658690 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884209 | ATACATTGTTCTGCA[C/T]TTTTTCGTTTAGTAG | 11060 |
rs764713641 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893945 | TTGAGCTAAGCTTGA[C/T]TGCTTTCTGGGCCCT | 11060 |
rs764719636 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848994 | ATATCAGATTTATTG[A/G]CTCCCTTGCCTTGGC | 11060 |
rs764720071 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932000 | CCTCCCAAAGCTCTC[A/G]TGCATCTTCAGGAAT | 11060 |
rs764727391 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836671 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 11060 |
rs764729346 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822738 | CAAGTCACACAGGAG[A/G]CCAACGGCAGGGAGG | 11060 |
rs764734182 | snp | A/G | 3.29881e-05 | 0.00406115 | intron-variant | WWP2 | GRCh38.p7 | 16:69840081 | GAATCTTAACTTGGG[A/G]TGCATTCTCTTTAGC | 11060 |
rs764741347 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903027 | GCAAAAGGAAAAAAT[G/T]ATATCAAAAAAGGTG | 11060 |
rs764747845 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868191 | TGTGTGTGTTGGGGG[G/T]TGGTGGCTGGCCACG | 11060 |
rs764765702 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879398 | AACCTGACCGGCCCC[C/T]GCCCACAGCCCATGG | 11060 |
rs764766748 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764731 | GTGTACACTAGCCAC[A/G]TGGGGCTGCTGAGCA | 11060 |
rs764790347 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925457 | TCGACTGACCATGAT[C/G]CCCTGGGCCCCCTCC | 11060 |
rs764808007 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940616 | CTCAGACTTTGTCCA[C/T]GTATAAACTTGAAGT | 11060 |
rs764830430 | snp | C/G | 1.66294e-05 | 0.00288347 | intron-variant | WWP2 | GRCh38.p7 | 16:69936461 | ACATCATGTGAGTCT[C/G]AGGCGCCGGGGGCTC | 11060 |
rs764845420 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817640 | TTTTACAATTACTAG[C/G]AGCACTTTTTGTTAA | 11060 |
rs764851757 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888364 | GTAGCCTCTGGGGAG[A/G]CTGCTGTGCATTGAA | 11060 |
rs764855295 | snp | G/T | | | missense | WWP2 | GRCh38.p7 | 16:69798763 | TGGATGGACTCCCCA[G/T]TGAGACCAAGAAGAC | 11060 |
rs764860976 | snp | A/G | 1.67899e-05 | 0.00289736 | missense | WWP2 | GRCh38.p7 | 16:69871820 | ACGCACAGACATTCG[A/G]GTGCTTCAGCCAGAA | 11060 |
rs764918449 | snp | A/G | 4.00008e-05 | 0.004472 | intron-variant | WWP2 | GRCh38.p7 | 16:69939830 | CTGTCGTGCTTCCCC[A/G]CTCTCAATAGCTTCA | 11060 |
rs764961004 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832436 | CAACCCATGATGCCA[A/G]TTTCATACCTAGAAA | 11060 |
rs764968126 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882662 | GGGTCGGGAGGGCGT[-/C]CAGGGAAGAAGGCCG | 11060 |
rs764990782 | snp | C/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925189 | CCCGTCGCTCTGCCT[C/T]TTCCAAAACTCACTT | 11060 |
rs764995911 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878390 | ATAGTGCAACTCAAC[A/C]AAACAAGGTATGCCT | 11060 |
rs765016669 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930353 | TTGGGTGGCCCCTGT[G/T]GTGCGTTCTACTGCC | 11060 |
rs765020972 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834622 | ACTTCTGTTTTCCGG[G/T]TTCAAGCGATTCTCC | 11060 |
rs765041058 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929189 | CCACCCCCTCCCTCC[-/G]ACCAATCAACCAAAG | 11060 |
rs765045319 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855195 | ACAGAACTAAAATCT[A/G]GAATTTATATTCTGC | 11060 |
rs765047720 | snp | G/T | 6.67111e-05 | 0.00577504 | intron-variant | WWP2 | GRCh38.p7 | 16:69798639 | GGGGGGCATCTGGGA[G/T]CCCTGGGACTCATCT | 11060 |
rs765071317 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813442 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 11060 |
rs765083364 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887823 | AAAGGTAGTGTTAAT[A/G]TATTTATTTCGGATT | 11060 |
rs765126770 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897550 | CATTTAAACTGCTAT[A/G]CGGTGTTCTGTTACA | 11060 |
rs765133692 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | WWP2 | GRCh38.p7 | 16:69798750 | GTGGAGGTGGCGGTG[A/G]ATGGACTCCCCAGTG | 11060 |
rs765137236 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843471 | AATCCCCAGATATTT[A/T]GAGGACATTTTGAGG | 11060 |
rs765171141 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917787 | CACCTGGCAGCGTCC[A/G]ACCGCGGAGTACGTG | 11060 |
rs765196189 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872776 | AGAGGAGACAGTGCC[A/G]TCCACGTGCGCATGG | 11060 |
rs765202463 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790195 | GAGGTTGCTGTGAGC[C/T]GAGACCACACCATTG | 11060 |
rs765214464 | in-del | -/TGT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916189 | AGTCAATGGAAGTGT[-/TGT]TGTTGTTGTTGTTGT | 11060 |
rs765221955 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917231 | CAATATCACCAAGGA[A/G]TTGGCTTTTCTCCCA | 11060 |
rs765224217 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819878 | TCCCCTTTCCACCTC[C/T]AGCCCCTGGCAACCA | 11060 |
rs765229877 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861386 | TTTTTTTAGTCTAAT[C/G]AAATTGCCACCTTTG | 11060 |
rs765250865 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850195 | ATTGAGACCATCCTG[A/G]CTAACACGGTGAAAC | 11060 |
rs765260175 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764310 | GGCTCGGGTGATCCT[-/C]CCATGTCTGCCTCCC | 11060 |
rs765269791 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819053 | AGGCTAAAATCCTCC[A/G]TGCCTTCCTTGACTT | 11060 |
rs765286428 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791388 | ACCTGCCACCACACC[C/T]GGCTAATTTTCGTAT | 11060 |
rs765295510 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900986 | TGCTTAGATTTAAAG[A/G]CTAGTTCCTTATTTC | 11060 |
rs765301741 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766361 | ACCCTGGCTGGCCTT[C/T]ACTTTCTCCACACAG | 11060 |
rs765308817 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896148 | TTTTTTGGAGACAGG[A/G]TCTCATTTTGTCACC | 11060 |
rs765309143 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906365 | GTGTCAGCCACCGCA[C/T]CCGGCCTTACGTATC | 11060 |
rs765313515 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882160 | GGGGTTTCACCATGT[C/T]GACCACACTGGTCTT | 11060 |
rs765319651 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862449 | TCAGCTCACTGCAGC[C/T]TCCATTCCCCAGGCT | 11060 |
rs765344547 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69838749 | GTTATTTTATAGAAA[C/T]GTTTAGTACTCACCA | 11060 |
rs765349696 | snp | C/T | 1.98837e-05 | 0.00315301 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69842032 | TTTCTAGGATCACAG[C/T]TGCCTTCGAGAGACT | 11060 |
rs765399359 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891454 | GATATATAAATGCAG[C/T]AGCTGAATTGAGTAT | 11060 |
rs765401568 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881616 | GGTGAAGACCATACT[A/G]TCTTTTCAGATTTTC | 11060 |
rs765407157 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931179 | TTCCCCTGGTGCTTA[C/T]GACCGCAGTTTTCGG | 11060 |
rs765412514 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827316 | GTAATAGGGTGCATT[C/T]TATAATGTCAGAGGT | 11060 |
rs765437085 | snp | A/T | 5.77128e-05 | 0.00537151 | missense | WWP2 | GRCh38.p7 | 16:69842105 | CCAGCACAAACTGCT[A/T]TGGTGGAAGATCCCG | 11060 |
rs765444857 | snp | C/T | 1.66054e-05 | 0.00288139 | missense | WWP2 | GRCh38.p7 | 16:69935881 | GAAAGTTCATCGACA[C/T]GGGCTTCACCCTCCC | 11060 |
rs765452925 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921903 | ACATGGTGAAACCCT[A/G]TCTCTACTAAAAATA | 11060 |
rs765475532 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796520 | CACTGCCGCTGCCCA[A/G]TAGTACCGCATATGA | 11060 |
rs765479376 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809195 | TGGAAAATGTGGATT[G/T]CAACAGGGCAGTGGG | 11060 |
rs765510354 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794907 | GTACTGAATTGGGGG[-/A]AAAAATGGCTTTAAA | 11060 |
rs765511006 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767696 | TATGTGGGGATTGAT[A/G]CATCTGAGGGCTGTT | 11060 |
rs765511212 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900609 | ATCACTGCATCCTCC[A/G]CCTCCTGGACTCAAG | 11060 |
rs765516995 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69928987 | CTCCATAAGGACCAC[A/G]CCCTGTAGGACAGAG | 11060 |
rs765518581 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860670 | TTGGAGCCTGCCTCC[A/G]TCCTGCTGAATTCCT | 11060 |
rs765543279 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901833 | GCGAGTCCCTGTAAT[A/C]CCAGCTACTCGGGAG | 11060 |
rs765555175 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937348 | AAAACTCCCACTTCG[A/G]CAGGGCAGATGGGTT | 11060 |
rs765564042 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770505 | TGCCTCGCCCTACGT[C/T]TCTTCATTTGTATCC | 11060 |
rs765584431 | snp | C/G | 4.94189e-05 | 0.00497062 | missense | WWP2 | GRCh38.p7 | 16:69888120 | CTGCTGCACCCTTGA[C/G]TGTGACCCCGAATCC | 11060 |
rs765615361 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785765 | CCGAGTAGCTGGGAT[A/T]ACAGGCACCCACTAC | 11060 |
rs765616095 | snp | A/G | 1.65334e-05 | 0.00287514 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931836 | ATGACCTGCGCCGCC[A/G]GCTCTACATCATCAT | 11060 |
rs765616341 | snp | A/C | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761893 | TGATCTTCAGATAAT[A/C]AAAAAATACTTTTTT | 11060 |
rs765628048 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886655 | ATCCTAGCTACTTGG[G/T]AGACTGAGGCATGAG | 11060 |
rs765629014 | snp | A/C | 1.64819e-05 | 0.00287066 | missense | WWP2 | GRCh38.p7 | 16:69888183 | CGGCTGAAGGAGAGG[A/C]ACCCAGCACTTCGGG | 11060 |
rs765634532 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858438 | AACTTCTGGGTGGGT[C/T]ATGTTGCTGGTTTAC | 11060 |
rs765677083 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774418 | GGCATGTGCCACCAT[C/G]GCTAATTTTTGTGGT | 11060 |
rs765698978 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828165 | TAAGGGTGGTCCTGG[A/T]TGGTGAGTCCGTTAT | 11060 |
rs765703845 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802909 | CGCATCTGGCCCAAG[A/T]TATCTTATTATGTAT | 11060 |
rs765746277 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903105 | CAGTTGAGGGGGTTC[A/G]TAGAAGGACATTGAG | 11060 |
rs765766092 | in-del | -/TTTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912567 | AAATTGGAGGGTAGT[-/TTTG]TTTGTTTGTTTGTTT | 11060 |
rs765777531 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895751 | GATGACTGAGTGAGA[-/C]CCTGTCTCAGTTAAA | 11060 |
rs765786871 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828974 | TTTCCCTGTCAGAAG[C/G]ACCTCAACATGTGCA | 11060 |
rs765787035 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935331 | GGGCACATTCTTCCC[A/G]GGTCTAGAGACCCGC | 11060 |
rs765791996 | snp | G/T | 1.6501e-05 | 0.00287232 | intron-variant | WWP2 | GRCh38.p7 | 16:69936279 | GACCCTGACACGGTA[G/T]ACATCTCCCCACTTG | 11060 |
rs765792574 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814538 | CCATGAAAGGTGAAG[C/T]TGATTTTGAAAAGCT | 11060 |
rs765794146 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845760 | TTCTTCAAGAATAAT[C/T]AGATGAAGCCTGGGC | 11060 |
rs765800615 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814199 | AAGGTCTTGCTCTGT[C/T]GTCTAGGCTGCAGTG | 11060 |
rs765805202 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876258 | CCTTTAGGAGGTTTT[G/T]AATGGGTTTTGGCCA | 11060 |
rs765810279 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884291 | CACCTCCCCTTTCCC[A/C]ACTAACTCCAGCCAA | 11060 |
rs765817665 | snp | C/G | 0.00194638 | 0.0311352 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931777 | AGGGAGAGTGGCAGG[C/G]TGGCCCGATGCTCTG | 11060 |
rs765832163 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806058 | AAAAAAAATTAGCCA[-/G]GGTGTGATGGTGTAC | 11060 |
rs765883152 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801073 | GGGCGCCTGTAATCC[C/T]GGCTACTCAGGACGC | 11060 |
rs765884695 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847784 | GAGAGGACATTAATT[G/T]ATTCATGAGGGATCC | 11060 |
rs765888258 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816264 | TGTGTAAAATTTCAT[A/G]TCATGTATATTTTAC | 11060 |
rs765894133 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894336 | TCTTCCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 11060 |
rs765903105 | in-del | -/C | 3.46732e-05 | 0.00416358 | intron-variant | WWP2 | GRCh38.p7 | 16:69917915 | TGGCCCGAGGTGGGG[-/C]CCGCCTCCCTGCGCT | 11060 |
rs766017753 | snp | A/G | 4.94752e-05 | 0.00497344 | missense | WWP2 | GRCh38.p7 | 16:69917804 | CCGCGGAGTACGTGC[A/G]CAACTATGAGCAGTG | 11060 |
rs766026586 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763303 | GTAACTAGGTAGGGT[G/T]CCTGAGAGGTCTGTG | 11060 |
rs766044082 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781241 | GAGGGTGGGGGGATA[C/G]TGGGGAGCAGGAAGT | 11060 |
rs766058922 | snp | C/T | 4.96003e-05 | 0.00497973 | intron-variant | WWP2 | GRCh38.p7 | 16:69939301 | TGCTTTGGGAAGGGA[C/T]GTCTCTGCTGACGTC | 11060 |
rs766064924 | snp | A/G | 4.73339e-05 | 0.00486464 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933175 | CGGACAGGATACCGG[A/G]GCACCCTCTGCGTCG | 11060 |
rs766095910 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896906 | TTTGCCTGGCACCAC[A/G]TATACAGATACACGT | 11060 |
rs766107776 | snp | A/C | 2.10307e-05 | 0.00324267 | intron-variant | WWP2 | GRCh38.p7 | 16:69842129 | GATCCCGGTAAGACC[A/C]CCCTTGGTGAGGACA | 11060 |
rs766110156 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864027 | TCTATGAGCTTTTGC[A/G]TACAGGCTTTTATGC | 11060 |
rs766138227 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768839 | TTAGTCTTTGTAAGG[A/T]TGTCATTTGGCAAAG | 11060 |
rs766150913 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877473 | CGCTTTCTCCCTATC[A/G]CTTTTCTTGGTAAGG | 11060 |
rs766154469 | snp | C/G | 6.17799e-05 | 0.00555753 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69933045 | CCTCCTCTCCAGGCT[C/G]TGCTTGGTGGGCTTC | 11060 |
rs766154808 | snp | C/T | 1.66239e-05 | 0.00288299 | intron-variant | WWP2 | GRCh38.p7 | 16:69937502 | AGCGAGTGGACGATG[C/T]GCGGGGAGGGACCTG | 11060 |
rs766182398 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924510 | TTTGACAACACCCCC[-/C]TTCCCCGCAGGATAT | 11060 |
rs766196076 | snp | A/G | 1.6817e-05 | 0.0028997 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871813 | CCCCAGGACGCACAG[A/G]CATTCGGGTGCTTCA | 11060 |
rs766197151 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777178 | CATATGGATATACAC[-/AT]ATGTGTATATACAAT | 11060 |
rs766198913 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880190 | ACATGTATATAAAAT[C/G]AGGACTGGGTCTAAA | 11060 |
rs766228640 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769833 | CCCATTTCCTGGCCT[A/G]TAACTCCTAAAATCA | 11060 |
rs766241020 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911611 | AAGGGCTGACTGGGC[C/T]TCCAGTCACTGTTCT | 11060 |
rs766242992 | snp | A/C | 1.65149e-05 | 0.00287353 | missense | WWP2 | GRCh38.p7 | 16:69937200 | AACGAGGTGGCCCCG[A/C]TGGAGTGGCTGCGCT | 11060 |
rs766277093 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926516 | GCAGGTTTGGAGCTG[C/G]ATCTTCTCGATGCAG | 11060 |
rs766278265 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835651 | TTTTTTTTCCTGAGC[C/T]ATTTGAAGGTAAATT | 11060 |
rs766283407 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811948 | TGGTTCCTAAAGGAG[A/G]AGGATACTACAGTAC | 11060 |
rs766283936 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907740 | ATTCTTTCAGTAGTG[-/C]ACATAAGCCATCCTC | 11060 |
rs766287861 | snp | C/T | 1.69092e-05 | 0.00290763 | missense | WWP2 | GRCh38.p7 | 16:69871883 | GCTCGGAGCCGGCAC[C/T]GCCAGCCCGTCAAGA | 11060 |
rs766320794 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868669 | ACATGTGCACACACA[-/CA]CACACACACACACAC | 11060 |
rs766336361 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833010 | AGGTGCACGCCACCA[C/T]GTCCAACTAATTATT | 11060 |
rs766351396 | in-del | -/CTT | 0.000414594 | 0.0143918 | intron-variant | WWP2 | GRCh38.p7 | 16:69798844 | TGTAAGAGAAAGCCC[-/CTT]CTTTTTGAACGCAGC | 11060 |
rs766364911 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935560 | GGCCAGGAGCCAGCC[A/G]GCCAGCGTGCGGGGC | 11060 |
rs766372524 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830867 | GACTCCAGCCTGTGT[A/G]TGTCTGAGTTTCAGG | 11060 |
rs766378894 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888458 | GGGCAGAATCAATGC[A/T]ACCTTGTACTGTGAC | 11060 |
rs766441478 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818257 | CTGTTGCCCAGACTG[A/G]AGTGCAGTGGTGTGA | 11060 |
rs766473794 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896911 | CTGGCACCACATATA[C/T]AGATACACGTATAAC | 11060 |
rs766501320 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938968 | AGAGAGCTCCACGTT[C/T]GGGCAAAGTACTGGG | 11060 |
rs766514705 | snp | A/G/T | 6.58983e-05 | 0.00573981 | missense | WWP2 | GRCh38.p7 | 16:69908835 | CCACCACCTGGGAGC[A/G/T]GCCCCTTCCTCCAGG | 11060 |
rs766531139 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806249 | TTCCTAATAGTAATT[A/G]TCTTAGAATTTCTAG | 11060 |
rs766540283 | snp | C/G | 1.65463e-05 | 0.00287626 | missense | WWP2 | GRCh38.p7 | 16:69937611 | AGCACCATCTACCGG[C/G]ACTACACCAAGAACA | 11060 |
rs766549407 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789994 | ACGCCTGTAATCCCA[A/G]CACTTTGAGAGGCTG | 11060 |
rs766565108 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882278 | CCTGTTTTGTAAATG[A/T]TATTGTTATACAAAT | 11060 |
rs766567537 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906410 | CTTCTGAGGGGCTGA[C/T]CAATGCAGTCCACTA | 11060 |
rs766596026 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861314 | CTAAGCCCAACATAC[A/G]GCCTGGAAGTAGATT | 11060 |
rs766606426 | snp | A/G | 0.00014191 | 0.0084223 | intron-variant | WWP2 | GRCh38.p7 | 16:69841987 | GAGTTGAGCTCCTCA[A/G]TGCTTCTGTCTTTTC | 11060 |
rs766633308 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790904 | TTATATATTTAAGGG[C/T]GGTTGTATTTCCTTT | 11060 |
rs766649550 | snp | C/T | 6.58903e-05 | 0.00573941 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934069 | GCAGATCAACCCCGC[C/T]TCCTCCATCAACCCG | 11060 |
rs766654419 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775246 | GGGTATAAGGAGGGC[A/G]TCTCTCAAAGGAGGG | 11060 |
rs766655077 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891630 | ACTGTTTCATGATGC[A/G]TGCCCTGGTCACTCA | 11060 |
rs766675827 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827533 | AAACTCCAATGTATA[C/G]AAGGGAATTTTTTTA | 11060 |
rs766707669 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929771 | CTGGCGGGTGTTGCT[A/G]GTCTCCATACTGATT | 11060 |
rs766708103 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917500 | CTTCCCCAGAACCAC[A/G]TGGATCCCCAAATTA | 11060 |
rs766714882 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766237 | CCTCTCACACCCCAC[A/G]TCCAACTCAGCTCGT | 11060 |
rs766717512 | snp | A/C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808259 | TGACCTTTTTTTGCA[A/C/T]GTGTCAATAGTCTTT | 11060 |
rs766732656 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796498 | GTGGCTGACTGGTGT[C/T]GCGGCTCACTGCCGC | 11060 |
rs766736020 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819851 | GATCCTTTGTGCCCA[C/T]TTATAGTGAATTCCC | 11060 |
rs766769329 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877963 | TAGGCGCGTGCCACC[A/G]TGCCCAGCTAATTTT | 11060 |
rs766776147 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805150 | GTTCAAGCGATTCTC[C/G]TGCCTCAGACTACTG | 11060 |
rs766785766 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | WWP2 | GRCh38.p7 | 16:69888102 | TTGGTGTGACGTCCC[C/T]ACCTGCTGCACCCTT | 11060 |
rs766857670 | snp | C/T | 3.29663e-05 | 0.00405981 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931555 | GCGTTTCCAGGCAGA[C/T]GCTTTTCGAAGATTC | 11060 |
rs766912179 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895426 | TCTGTTCAATGAGAC[A/G]AATCTATTGAGCACA | 11060 |
rs766917559 | snp | A/G | 0.000136696 | 0.00826616 | missense | WWP2 | GRCh38.p7 | 16:69939114 | GTCGGGGGATTTGCC[A/G]AACTCATCGGTATGT | 11060 |
rs766923221 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937522 | GGAGGGACCTGCCGG[A/G]GATGCTGACTGCCGC | 11060 |
rs766923825 | in-del | -/ACACACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885144 | CACACACACACATTC[-/ACACACA]TTCTTCTTTAGAATG | 11060 |
rs766940432 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856653 | GTGGCATGTGCCTGT[A/G]GTCTCAGCTACTCGG | 11060 |
rs766943135 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902171 | TTGGGAAACCTTTGA[C/T]AAGAAAACATGGTTC | 11060 |
rs766945833 | snp | A/C | 3.29598e-05 | 0.00405941 | missense | WWP2 | GRCh38.p7 | 16:69936365 | TCATCCAGGACATGG[A/C]GATACTGGGCAAGGT | 11060 |
rs766946925 | snp | A/C | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69839843 | CACAGTCCTGCAAGT[A/C]TAAACAAACTAATAC | 11060 |
rs766964772 | in-del | -/CTTACTGCACCCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852348 | ATGGTGTGATCTCGG[-/CTTACTGCACCCT]CCACCTCCTAGGTTC | 11060 |
rs766977939 | in-del | -/TTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817662 | TTTTGTTAAACTCTT[-/TTTTTTTTTTT]TTTTTTTTTTTTTAA | 11060 |
rs766996953 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929479 | TGGACGGGTGTATTA[C/T]GTGAACCATAACACT | 11060 |
rs767022121 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886773 | TCAAAACAAAACAAC[C/T]CCTCACCAACTTTCT | 11060 |
rs767026070 | snp | A/G | 1.73697e-05 | 0.00294696 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931938 | ACCCCGCTTCCCCAG[A/G]CTACAGCATCAATGG | 11060 |
rs767032790 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900771 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 11060 |
rs767056330 | snp | A/G | 1.67225e-05 | 0.00289154 | intron-variant | WWP2 | GRCh38.p7 | 16:69798879 | GATGGGGAAAGAGAG[A/G]GGGTGCTCCGAGGGG | 11060 |
rs767090193 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835717 | CCCTATTCTTCTAAA[A/G]AGTCACTTGAAAATA | 11060 |
rs767090543 | snp | A/G | 1.64961e-05 | 0.00287189 | missense | WWP2 | GRCh38.p7 | 16:69798789 | AAGACTGGGAAGCGC[A/G]TTGGGAGCTCTGAGC | 11060 |
rs767111072 | in-del | -/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909990 | ATATTTGTTGACTTA[-/T]TGTTTTTGGCTGTTT | 11060 |
rs767114216 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885976 | CAGTAGATGATATCT[C/T]GAAGAGGGCAGCCAG | 11060 |
rs767124855 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909077 | GCGCATGGGAGGCCA[A/G]GATTTAGAGTGTTGA | 11060 |
rs767127471 | in-del | -/ACTTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894941 | TTGGACTGCCGACTT[-/ACTTC]AGCTCTGCCATTTCA | 11060 |
rs767132230 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780929 | GCTACTCAGGAATCT[A/G]AGGCGGAAGGATCAC | 11060 |
rs767145264 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837434 | TGAGCCTTCAAATAT[A/G]TAATGATTCCACTGG | 11060 |
rs767150713 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862916 | AATTTTTTATGGAGA[C/T]GAGGTCTCCCTGTGC | 11060 |
rs767168956 | snp | A/C | 1.66763e-05 | 0.00288753 | intron-variant | WWP2 | GRCh38.p7 | 16:69917705 | CTGAGGTTCCTATTT[A/C]CAGCTGGGAAAAACG | 11060 |
rs767170171 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888094 | TTCCGTTGTTGGTGT[A/G]ACGTCCCCACCTGCT | 11060 |
rs767177393 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792334 | TTGAGAGAGCAGATG[C/T]CAGACTCTATTGTGG | 11060 |
rs767188787 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845912 | AAAATTAGCCAGGCA[-/TG]GTGGTGTGTGCCTAT | 11060 |
rs767204349 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894997 | GCCATTGGCTGCCCC[A/G]TCTGTTTCCTGCCTC | 11060 |
rs767212267 | in-del | -/CTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803210 | CTTTTTTGCTCTGAT[-/CTC]CTGGCCTCTCAATAA | 11060 |
rs767295671 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932954 | GTTGGGTTAACTTGC[C/T]TCTGGTCCTCTGTTC | 11060 |
rs767300306 | in-del | -/T | 1.64776e-05 | 0.00287028 | intron-variant | WWP2 | GRCh38.p7 | 16:69840103 | TCTTTAGCCCATCCA[-/T]TGTTGCCTTTTGTAC | 11060 |
rs767313520 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932190 | CACAATTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 11060 |
rs767329750 | snp | C/T | 1.69301e-05 | 0.00290942 | intron-variant | WWP2 | GRCh38.p7 | 16:69936504 | GGCGTGGAGATCTAG[C/T]GGGTTGCAGAGAAAG | 11060 |
rs767342109 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834737 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCAAACT | 11060 |
rs767347861 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870246 | ATAATGTTAGAGTTC[A/G]GTGAATATTATATAC | 11060 |
rs767359680 | snp | G/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940835 | AGCCTGGCAGGGACC[G/T]CGTCCCCAAGCCTGG | 11060 |
rs767368639 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863869 | GCGGTTGTGATTCAC[C/T]TCTGTTGCTGCATGT | 11060 |
rs767373799 | snp | A/G | 6.02973e-05 | 0.00549045 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939949 | GGAGTAACCGAGGCC[A/G]CCCCTCCCACGCCCC | 11060 |
rs767387248 | snp | G/T | 1.64912e-05 | 0.00287147 | missense | WWP2 | GRCh38.p7 | 16:69917796 | GCGTCCGACCGCGGA[G/T]TACGTGCGCAACTAT | 11060 |
rs767387796 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913419 | AGGTGGGAGAATCAG[C/T]TGGGCCTGGAAGGTT | 11060 |
rs767404909 | in-del | -/TCTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817658 | CACTTTTTGTTAAAC[-/TCTTTTTTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs767428344 | snp | C/G | 1.66371e-05 | 0.00288414 | intron-variant | WWP2 | GRCh38.p7 | 16:69787124 | TTGTCTACGCCCAGG[C/G]AAGAGGGAGAATCTA | 11060 |
rs767441393 | in-del | -/G | 6.65264e-05 | 0.00576704 | intron-variant | WWP2 | GRCh38.p7 | 16:69929548 | GGACTTGGGCTGAGA[-/G]GGGGGGCCGGGCTGG | 11060 |
rs767519385 | snp | G/T | 6.58935e-05 | 0.00573955 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931163 | CTAGGACGAAGCAAG[G/T]TTCCCCTGGTGCTTA | 11060 |
rs767525846 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880578 | AACACAGTATGGCTT[C/T]GTCCATTTTTAAGTT | 11060 |
rs767531401 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890140 | TTTTTTTTTTTTTTT[-/G]TAGAGACAGGGTTTT | 11060 |
rs767536976 | snp | A/G | 3.30017e-05 | 0.00406199 | intron-variant | WWP2 | GRCh38.p7 | 16:69908715 | CTAACAGGGGCCTAT[A/G]CCTTTCCACTGTGTG | 11060 |
rs767557415 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789188 | TCAGCCTTCCAAGTA[A/G]CTGGGATTACCAGTG | 11060 |
rs767561938 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926241 | TAGAGATGATGAGAC[-/TT]AGCGCATTTGATAGA | 11060 |
rs767593201 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810326 | CTGGCCATGGCTGCA[A/G]AAAGACTTGCCCAAA | 11060 |
rs767615663 | in-del | -/TAGA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781014 | CCTGGGTGACAGGGC[-/TAGA]TAGACCCTGTCTCAA | 11060 |
rs767624734 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | WWP2 | GRCh38.p7 | 16:69840097 | TGCATTCTCTTTAGC[C/T]CATCCATGTTGCCTT | 11060 |
rs767693357 | snp | C/T | 1.65433e-05 | 0.002876 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937604 | GCAGAAGAGCACCAT[C/T]TACCGGCACTACACC | 11060 |
rs767714165 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799517 | TAATGTGATGCAGTG[A/G]TGTGTTGCCCTTTAT | 11060 |
rs767722262 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897867 | GAGCCGAGATCGTAC[C/G]ACTGCACTCTAGCCT | 11060 |
rs767735713 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776093 | TATGGGGGAGGGGAA[A/G]CATTCTATAGCCTCA | 11060 |
rs767743806 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936873 | TACGTCTGAGGTTCA[A/G]TCGGCGCTGGGGGCA | 11060 |
rs767774692 | snp | A/G | 3.29717e-05 | 0.00406015 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931542 | CACGTGAAGATCAGC[A/G]TTTCCAGGCAGACGC | 11060 |
rs767815623 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905637 | TGGTCCCAAGCATCT[A/G]GAGAAGGGGCTACTC | 11060 |
rs767818480 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818119 | GTCTTTTTAACTTAC[C/T]TTAGTCTGTTAGGCA | 11060 |
rs767826641 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808487 | GCTCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 11060 |
rs767837464 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884075 | CCTCCAAGGCCCACT[G/T]TTGTGTTTCTTGCGG | 11060 |
rs767845781 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807193 | GGCACACGTCACCAT[G/T]CCCGGCTAATTTTGT | 11060 |
rs767847928 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930799 | ATCGCTTAAGACCAG[G/T]AATTCGAGGCCGCAG | 11060 |
rs767859747 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840184 | AGGCAGCGTTGTCTC[A/G]GGCGGAGAGCTGACA | 11060 |
rs767862694 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | WWP2 | GRCh38.p7 | 16:69936352 | CTGGAGCTGTACTTC[A/G]TCCAGGACATGGAGA | 11060 |
rs767863001 | snp | C/T | 5.07078e-05 | 0.00503501 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931476 | TGACCACTTGAGGCT[C/T]GATTTAAAGTTCTTT | 11060 |
rs767868863 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824227 | TCATTTATCTCATTG[C/T]AGTGTTTAATTTTCC | 11060 |
rs767871012 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801816 | TTTTATATTTGTAGA[C/G/T]GTATATTGATGTTTA | 11060 |
rs767903816 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815788 | CAAGACTCCGTCTCG[-/A]AAAAAAAAAAAAAAA | 11060 |
rs767918642 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860232 | GTGATGAGTGACTGG[A/G]TTGGAAAGAATATGC | 11060 |
rs767927042 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859122 | TAAAACAACACCATT[G/T]ATTAGCTCACAGTTC | 11060 |
rs767932515 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764950 | GGCTCATGCCTATAA[G/T]TCCAGCACTTTGGGA | 11060 |
rs767952836 | snp | A/G | 1.65072e-05 | 0.00287286 | intron-variant | WWP2 | GRCh38.p7 | 16:69936271 | CCAGGAAAGACCCTG[A/G]CACGGTAGACATCTC | 11060 |
rs767991582 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940328 | TTCGGCGAGGAGACT[A/G]GCCACTGGGGGTGGC | 11060 |
rs768010310 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849069 | TTATAAAGCCTAACC[A/G]TCTCCGGTGAGCTCT | 11060 |
rs768013642 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862972 | GCTCAAGCAGTCCTC[C/T]GCCCTTGGCCTCCTA | 11060 |
rs768022466 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766045 | TCTCGAGACTTCTAG[A/G]TCTAATTGCCCACAA | 11060 |
rs768048169 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69839630 | TCAAGACAATACATT[C/T]TCAGGATTGAAAATT | 11060 |
rs768051952 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867161 | TTTTTTTTTTTTAAA[C/T]CAAACAAACAAAATC | 11060 |
rs768094842 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929908 | TGGCTGCTCAGTCCA[A/G]TGCCATCCATGCAGG | 11060 |
rs768098738 | snp | A/T | 1.65345e-05 | 0.00287524 | intron-variant | WWP2 | GRCh38.p7 | 16:69939290 | CCGGAGGATCCTGCT[A/T]TGGGAAGGGACGTCT | 11060 |
rs768112203 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767295 | TTGTCAGGCATCCCA[C/T]CATTTTATACATTTA | 11060 |
rs768133574 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791157 | TGGCCTATTGGACCT[A/G]GTAACATCCTGAGGT | 11060 |
rs768135459 | snp | C/G/T | 5.05918e-05 | 0.00502929 | intron-variant | WWP2 | GRCh38.p7 | 16:69929426 | TTGAATCTGATGTTC[C/G/T]TTCTTTCTTCTCATG | 11060 |
rs768136487 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827761 | CAGGGCCTGGGCAGG[A/G]GATTAATGGTGTGGC | 11060 |
rs768157616 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795802 | ACTGTTGTGCCCCAC[C/G]ACGCCCAGCTAGTTT | 11060 |
rs768171630 | snp | C/T | 1.84218e-05 | 0.00303489 | missense | WWP2 | GRCh38.p7 | 16:69842060 | ACTCCAGTGGAACAG[C/T]AGTAGCTCCAGAGAA | 11060 |
rs768202289 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768205 | GATGATGGGACAGGT[C/T]AGATTCTAACCAAAA | 11060 |
rs768202889 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768395 | GGGTAGATCACCTGA[A/G]GTCAGGAGTTTAAGA | 11060 |
rs768209450 | snp | C/T | 3.30284e-05 | 0.00406363 | missense | WWP2 | GRCh38.p7 | 16:69937195 | GCTTCAACGAGGTGG[C/T]CCCGCTGGAGTGGCT | 11060 |
rs768227840 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888308 | ACTGAGGCTCCTTTA[C/T]GGGGGTGGAAACAAC | 11060 |
rs768247689 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796306 | CCTGAAAAACCCATC[A/G]TAAGTTGAACATATC | 11060 |
rs768248926 | snp | C/T | 0.000115328 | 0.0075928 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931147 | AACATCTTTGCTCTT[C/T]CTAGGACGAAGCAAG | 11060 |
rs768297386 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840394 | CCTGGCCCATAGCTA[A/G]CCCGGACTCTTCTTA | 11060 |
rs768314847 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934397 | AAGCTAGAGAGAGTT[C/G]TGGAGAAACCAGAGC | 11060 |
rs768319509 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897505 | TGATCTCATTCCCTG[C/T]ATACAGTGATACATG | 11060 |
rs768321664 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931249 | TCTGGTACTGGGGCT[C/T]CCGTGGCAGTTGGGG | 11060 |
rs768339492 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937721 | AACGGGTCCTGAGGA[C/G]GCCTCACGCGCAAGG | 11060 |
rs768342715 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858941 | CCACAGAGTGATGCC[A/G]TAACTGTATGAGGGC | 11060 |
rs768349862 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797170 | TGTGATGCTTGTGTA[G/T]CTTTGTACTCCATGA | 11060 |
rs768359017 | snp | A/C | 1.64765e-05 | 0.00287019 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888157 | GACTTCTCTCCCTGC[A/C]CCAGCCACACCGGCT | 11060 |
rs768372983 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940317 | TCCTGGACTAGTTCG[A/G]CGAGGAGACTGGCCA | 11060 |
rs768387711 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69775121 | GAAATACGATTGGAC[A/G]AAAGGGGTATGATTG | 11060 |
rs768411191 | snp | G/T | 1.65067e-05 | 0.00287282 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929471 | CAGGACAATGGACGG[G/T]TGTATTACGTGAACC | 11060 |
rs768411815 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935954 | CCTGGAGTCCATTGA[C/T]CCTGAGTTCTACAAC | 11060 |
rs768424036 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807349 | CTATCCTTGTCTATT[G/T]TTGTTTAATAATGAA | 11060 |
rs768431903 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883729 | CTCTCCCTCCCCGCA[A/C]CCCACCCTGCAAAAA | 11060 |
rs768433959 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | WWP2 | GRCh38.p7 | 16:69888075 | CCACTGATCCCGAAG[A/C]ACCTTCCGTTGTTGG | 11060 |
rs768451025 | snp | A/T | 1.6516e-05 | 0.00287362 | stop-gained | WWP2 | GRCh38.p7 | 16:69799203 | AGAGTCATTTAGATT[A/T]AAAGGTCTGGAGCTG | 11060 |
rs768460930 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773634 | TACAGGCATGCACCA[C/T]CATGTCTGACTAATT | 11060 |
rs768461489 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762937 | ACAGAATCTTGATCG[C/T]CTTGCTTCCCTCGCG | 11060 |
rs768468487 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906821 | AGAATCAGAGGCTGT[A/G]GTGAGCTATGATCAC | 11060 |
rs768504698 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803388 | AAACATTATCTTACA[A/C]AATTACTGTATCGTT | 11060 |
rs768521922 | snp | C/G | 1.66493e-05 | 0.0028852 | intron-variant | WWP2 | GRCh38.p7 | 16:69798861 | TCTTTTTGAACGCAG[C/G]AAGATGGGGAAAGAG | 11060 |
rs768539237 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820923 | TCCTGTGACTTAGGT[C/T]TTTGCAGCCAGTGTC | 11060 |
rs768571817 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780745 | GAAATGGCTCATGCC[-/T]GTAATCCCAGCACTT | 11060 |
rs768593038 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804317 | TTTTTTCCTGGGTGT[C/T]TATGATTTTATTTTT | 11060 |
rs768602716 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890542 | TGTATGTTATAATTT[-/G]GGGGGGAACAATGCA | 11060 |
rs768622976 | snp | A/C | 1.64857e-05 | 0.00287099 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931539 | AGCCACGTGAAGATC[A/C]GCGTTTCCAGGCAGA | 11060 |
rs768634216 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902713 | CTCTGACAGGGATGC[A/G]CTGATGAAAAATTGA | 11060 |
rs768658691 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925433 | TCTTGTGTTTAGTCT[C/T]CGAGTGCTTCGACTG | 11060 |
rs768669307 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929650 | GGGACCTTTAGCCAC[A/C]CACAAGTGTCTTGAG | 11060 |
rs768682107 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937303 | CCTGCTCTGTGATAC[A/G]CTCACTGTGTACCCA | 11060 |
rs768693290 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814474 | TTTACAAATTCCTTC[A/C]CATCTGTAATGCACA | 11060 |
rs768695948 | in-del | -/TAATCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843491 | ACATTTTGAGGAAAA[-/TAATCT]TAAATGTACAAACTA | 11060 |
rs768708446 | snp | C/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909562 | TTTAGCTCCAGTTTT[C/G]CAGTAGAATGCTTGA | 11060 |
rs768720990 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865632 | GTTGGCTAAGTTTAC[A/G]TATTTATCAGGTTAT | 11060 |
rs768731278 | snp | C/G | 2.1896e-05 | 0.0033087 | intron-variant | WWP2 | GRCh38.p7 | 16:69871945 | AGGTGAGTGATGGCA[C/G]CGCACGCCAGCCTGC | 11060 |
rs768731876 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901603 | TATTTTGAGTAGAGA[C/T]GGGGTTTCACATGGT | 11060 |
rs768737926 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919359 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTAGT | 11060 |
rs768746283 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815975 | GTTGCCCAGGCTGGC[-/A]ATTTTAAACTTAAAT | 11060 |
rs768751912 | snp | A/G | 1.79735e-05 | 0.00299774 | intron-variant | WWP2 | GRCh38.p7 | 16:69937703 | GGGCCATCAACCAAA[A/G]GAAACGGGTCCTGAG | 11060 |
rs768758118 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834445 | TCCCAGCTTAACATT[A/C]TTCATCCCCCTTCTT | 11060 |
rs768769806 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783248 | CTCCTGACCTCAAGT[A/G]ATCTGCCTGCGTTGG | 11060 |
rs768772391 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819168 | CTGTCACCCATGTCC[A/G]AGTCACTTCTTGACT | 11060 |
rs768780346 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811661 | TGGGAGGCTGAGGTG[A/G]GAGGATCACTTGGGC | 11060 |
rs768783869 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811437 | CATAGTGAGACCCAT[-/G]CCACCCCTCCATCCC | 11060 |
rs768798483 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922589 | GCTCCACGTAACACC[G/T]TGACATCTCTCATTT | 11060 |
rs768806279 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794821 | CATTGCCATGGAAAA[G/T]AAGGGAGGATGTTCT | 11060 |
rs768814060 | snp | C/T | 4.99089e-05 | 0.00499519 | intron-variant | WWP2 | GRCh38.p7 | 16:69939797 | GGGGCTATCAGAGCC[C/T]TGGCCTCCTAGGGCT | 11060 |
rs768819897 | snp | C/T | 4.94319e-05 | 0.00497127 | missense | WWP2 | GRCh38.p7 | 16:69936331 | AACAACCTGGAAGAA[C/T]GTGGCCTGGAGCTGT | 11060 |
rs768820992 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69798728 | TCAACCTCGAATTAA[C/T]TCCTACGTGGAGGTG | 11060 |
rs768828029 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853768 | GCATGGCTGGCTAAT[C/G]AGACAAGGTGAAGGG | 11060 |
rs768844177 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836003 | AGATGGGGTTTCACC[A/C]TGTTGGCCAGGCTGA | 11060 |
rs768846110 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822283 | TGAGCCTTGCTTGTA[A/G]CAGGGGCAGGGCCTG | 11060 |
rs768851970 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824768 | CTTTGCACCTGTGGC[-/TTT]TTTTTTTTTTTTTTT | 11060 |
rs768853226 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810123 | CATTCTCCTCTTCCA[C/T]GGACAGAATTCGTTC | 11060 |
rs768885048 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877725 | AGGCCAATGTAGGGT[A/G]TAAGGAGAGAGAGAG | 11060 |
rs768917951 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854524 | AAACGTTGAATCAAT[G/T]CTGTATGTAGGCTTT | 11060 |
rs768917989 | snp | A/G | 3.73881e-05 | 0.0043235 | missense | WWP2 | GRCh38.p7 | 16:69842093 | GGCACCAGCCCCCCA[A/G]CACAAACTGCTTTGG | 11060 |
rs768936733 | in-del | -/CTCTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817657 | GCACTTTTTGTTAAA[-/CTCTTTTTTTT]TTTTTTTTTTTTTTT | 11060 |
rs768942102 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783301 | AGGCGTGAGCCACTA[C/T]GCCTGGCCAAGGGCT | 11060 |
rs768947288 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911248 | TCCTTCTATCCGGGA[A/G]CAATAAGTATTGGAC | 11060 |
rs768968920 | snp | C/T | 1.6585e-05 | 0.00287962 | intron-variant | WWP2 | GRCh38.p7 | 16:69787114 | TGTCTTCATCTTGTC[C/T]ACGCCCAGGGAAGAG | 11060 |
rs769007921 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842976 | ATCTGACTTATTTTT[A/T]ATTCTTTTTTATGGT | 11060 |
rs769042617 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | WWP2 | GRCh38.p7 | 16:69908790 | AGCTGCCCAACGGAC[A/G]TGTCTATTATGTTGA | 11060 |
rs769063026 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789793 | TTCTCAGTGTAGTTT[C/T]ATTTCCCACTTCTTT | 11060 |
rs769074072 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895574 | TTCGAGACCAGCCTG[A/G]GCAACATAGCAAGAC | 11060 |
rs769078443 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831205 | TCTTGTTTCATGTTT[C/G]TCAAATTTCCAGGTA | 11060 |
rs769090874 | snp | A/G | 1.67489e-05 | 0.00289381 | intron-variant | WWP2 | GRCh38.p7 | 16:69937285 | CCCTGCCTCTGGGGC[A/G]ATCCTGCTCTGTGAT | 11060 |
rs769099289 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770245 | CCAGTGGCCAGGGAA[A/G]CCAGCCTTGTAGTTA | 11060 |
rs769100523 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870930 | AATTCCACACTTTTC[A/T]TTGTGATTTCTGCAT | 11060 |
rs769101081 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861013 | GAGGCTTTTCTGGCG[C/T]ACCTGTACAGGTTGT | 11060 |
rs769115138 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881018 | ACTAGAGTGTGTCCC[A/G]GTCCTGAATGAATAT | 11060 |
rs769147952 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844024 | TTGTGGGCTTATGAG[A/G]TTGTGGTGACTGGCA | 11060 |
rs769151521 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830721 | CCTAGCTGGGTAGAA[A/G]AGACTTTCTGTTGTT | 11060 |
rs769173444 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842016 | TCTTGTGATTGATTC[C/T]TTTCTAGGATCACAG | 11060 |
rs769176530 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790196 | AGGTTGCTGTGAGCC[A/G]AGACCACACCATTGC | 11060 |
rs769209236 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890600 | ATGGCCGCCTGTGTC[C/T]CCAGTGAGCTGTTTG | 11060 |
rs769226686 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69908785 | GCGAGAGCTGCCCAA[C/T]GGACGTGTCTATTAT | 11060 |
rs769227972 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769218 | GCTACTCGGAAGGCT[A/G]AGGCAAGAGAATTGC | 11060 |
rs769228358 | in-del | -/TC | 1.88035e-05 | 0.00306617 | intron-variant | WWP2 | GRCh38.p7 | 16:69888277 | CTGTCCCATAACAGA[-/TC]TCTCCTCCTCAAAGA | 11060 |
rs769233546 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818731 | TTTCTGTCCATCTCT[C/G]TGGTCACTCTCATTC | 11060 |
rs769244866 | snp | A/G | 4.36729e-05 | 0.00467274 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933130 | CCTATGGTAGGTTAC[A/G]TCATGCTGTTCTACC | 11060 |
rs769293977 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914563 | AGGAGTTCAAGACCA[G/T]CCTGGGCAACACAGT | 11060 |
rs769308303 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931135 | CATGAACCCCTGAAC[A/G]TCTTTGCTCTTCCTA | 11060 |
rs769333666 | snp | A/G | 3.4035e-05 | 0.00412509 | missense | WWP2 | GRCh38.p7 | 16:69939920 | GCCATTGAGGAGACC[A/G]AGGGCTTTGGACAGG | 11060 |
rs769335447 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767943 | TTTGAGCTCAAGTGA[A/T]CCTCCCATCTTAGCC | 11060 |
rs769336623 | snp | A/G | 5.18202e-05 | 0.00508993 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931928 | GCTGCCCTGTACCCC[A/G]CTTCCCCAGGCTACA | 11060 |
rs769347287 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779210 | CCTGCCTCGGCCTCC[C/T]GAAGTGCTGGGATTA | 11060 |
rs769368212 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880090 | CGTTATCAAAATAAA[C/T]ATCCCATTAGAATTT | 11060 |
rs769370605 | in-del | -/CT | 1.65002e-05 | 0.00287225 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908879 | TGAGAAGACCTGAGA[-/CT]CTGGAACTGACACCA | 11060 |
rs769381131 | snp | A/C | 1.64977e-05 | 0.00287203 | intron-variant | WWP2 | GRCh38.p7 | 16:69934133 | TTCATCGCCATGGTA[A/C]GGGGGCCCCAGGGGT | 11060 |
rs769382011 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926971 | TGGGTTTTCATGCCA[G/T]TTCTGCTGAGTGATG | 11060 |
rs769384307 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837901 | AAGTCTCAGAAGGAT[C/T]AGAAGGATCAAGAGA | 11060 |
rs769402104 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806475 | ACAGTCTCTATAACA[A/T]GGGAATTATCTGTTC | 11060 |
rs769421139 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887586 | AAATTTTGTATTTTT[A/G]GCAGAGACGGGGTTT | 11060 |
rs769434121 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880303 | TGATCACTTTTAACA[G/T]TCTTACATACAGTGA | 11060 |
rs769449864 | snp | C/G | 1.76437e-05 | 0.00297011 | intron-variant | WWP2 | GRCh38.p7 | 16:69935821 | GTGCCCAGGGAAGGC[C/G]AAACCTCTGTGCTGT | 11060 |
rs769458291 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant | WWP2 | GRCh38.p7 | 16:69840269 | CTGACAGATGGTGAG[C/T]GCCGCCCTGCTCCTC | 11060 |
rs769465645 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926370 | TAGGCCAGCAGAAGA[C/T]GGTAAACGTTGGTTT | 11060 |
rs769470654 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766901 | TGGGATTACAGGCAT[C/T]TGCCACTATGTCCAA | 11060 |
rs769472114 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825962 | TACTATGGAAAATTT[C/G]AAACATAAATAAAAG | 11060 |
rs769475181 | snp | A/G | 5.19989e-05 | 0.0050987 | intron-variant | WWP2 | GRCh38.p7 | 16:69937689 | TGGCAGGGACATTTG[A/G]GCCATCAACCAAAGG | 11060 |
rs769494098 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807559 | AGGAGGCTGAGGCTG[C/T]AGCGAGTTGTTATTG | 11060 |
rs769507581 | snp | A/G/T | 4.95212e-05 | 0.00497579 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929469 | GACAGGACAATGGAC[A/G/T]GGTGTATTACGTGAA | 11060 |
rs769515135 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875501 | CGACGCTGTTTGACA[A/G]CATTTTAGCAACAGT | 11060 |
rs769521975 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69786772 | TCTTAGTAGACTCTG[C/T]CTCCTCTAGACTTTG | 11060 |
rs769547870 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814187 | TTTGTTTTTGACAAG[C/G]TCTTGCTCTGTCGTC | 11060 |
rs769568904 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827580 | CTTAAAAAATAATTT[C/T]CTAAGAGGACTCCTA | 11060 |
rs769571051 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849792 | CAGCCTGGACAACAT[-/A]GGGAGACCCTGTCTC | 11060 |
rs769572579 | snp | A/G | 3.43554e-05 | 0.00414446 | intron-variant | WWP2 | GRCh38.p7 | 16:69929399 | CAGGGAAAGGACACC[A/G]GCTCTCCGTGTTTGA | 11060 |
rs769591274 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855678 | CATGAGGATATCTGG[G/T]GAAAGAGAGTTTGGG | 11060 |
rs769594193 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888064 | ACCCACAACAGCCAC[C/T]GATCCCGAAGAACCT | 11060 |
rs769604648 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69917330 | CCCCAGGACCACATG[C/G]TTCCTCAGTCATATT | 11060 |
rs769625340 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898443 | AACCAATTCATACTC[C/T]TGTGAGCATGCATAA | 11060 |
rs769639010 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802447 | CTGGCAGCTACCGCT[A/C]TACTTTCTGCTTCTG | 11060 |
rs769654944 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828515 | GGGATCACAGGCATG[A/C]ACCACCACACCCCGC | 11060 |
rs769694734 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802559 | ATAATGTCCTCAAGG[C/G]TTATTCATGTTGTAA | 11060 |
rs769718292 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907600 | TATAGGTTACTATAT[C/T]CTGGGTAAGTAGAGT | 11060 |
rs769742356 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815282 | TGCTGGGATTACGGG[C/T]GTGAGCCACCTCACC | 11060 |
rs769743097 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781647 | CCGCTGGCTTTTACT[C/G]TGAGTTAGACGGTGT | 11060 |
rs769772696 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876175 | GTGGGCCAGTCTGGT[C/G]TTGAACTCCTGACCT | 11060 |
rs769785380 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882881 | CAGCAGACCGGGTGC[A/G]GTGGCTCATGCCTGT | 11060 |
rs769787214 | snp | C/G/T | 3.32575e-05 | 0.00407773 | intron-variant | WWP2 | GRCh38.p7 | 16:69798856 | CCCCTTCTTTTTGAA[C/G/T]GCAGCAAGATGGGGA | 11060 |
rs769810399 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868850 | ATGAAGTGGGAACTT[G/T]GAAATATTCATCTTT | 11060 |
rs769827295 | snp | A/G | 1.64972e-05 | 0.00287199 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931611 | CCGAAACCAGTGGCA[A/G]GCCGACGCCCTCCTC | 11060 |
rs769852109 | snp | A/G | 4.31788e-05 | 0.00464624 | intron-variant | WWP2 | GRCh38.p7 | 16:69939148 | CTCTCGCCCTCTGGC[A/G]TCCTGGCTGGCAGTG | 11060 |
rs769854058 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834311 | AGCACCTCTGGGCTT[C/G]CTTTTTCCTCTGCCT | 11060 |
rs769856069 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810757 | ACTAGAGGAATTTTC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs769865557 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902801 | TCTATGTGAGTCAGC[A/G]GCCACTGAGGAGGAA | 11060 |
rs769875182 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892459 | GCCCACTTGGCTACA[A/T]GCTTTTGCAATATTC | 11060 |
rs769886944 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925392 | TTCACCAGTGGCTTT[C/T]TGTAACCTCTGTGTT | 11060 |
rs769909215 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794011 | CACTTTCTGCCTCCT[A/G]GGTTCAAGCGATTCT | 11060 |
rs769910815 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69833645 | GAAGGGTGCAGTCGT[A/G]TAGCTGAAGAAGTAT | 11060 |
rs769913051 | snp | C/T | 3.29881e-05 | 0.00406115 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939348 | GATCACAGGTAGCAA[C/T]GGACCACAGAAGTTT | 11060 |
rs769949633 | snp | C/T | 1.67181e-05 | 0.00289115 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917880 | CCAAAGATTCCTCTA[C/T]CAGGTGAGAGGGCAG | 11060 |
rs769961635 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792054 | AGAGAGAAATAACCA[C/T]TTAAATAGCGTAGGT | 11060 |
rs769964887 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69852575 | TGCCTTGCCCGGCCT[A/G]TGATATGGAGAGTCT | 11060 |
rs769974344 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793037 | GTAATCACCCAGTGG[G/T]TTCTTCTTGCCCACT | 11060 |
rs769996888 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821401 | ACGAATGTTCCAACA[A/G]TCCTGCACCCTGTGT | 11060 |
rs769999485 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779986 | TTAATGAATATGAAC[-/A]TTTTGCCATATTTGC | 11060 |
rs770016215 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768541 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 11060 |
rs770024129 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938360 | GGCTTTCCACTTTGG[A/G]TTCCTTGGCTTCCCA | 11060 |
rs770050780 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775395 | TGCCAAGGTGTCATG[-/T]TTTGGGGTAAGGTAT | 11060 |
rs770057778 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840975 | GGAATCTCAGTGGCC[A/G]GATGGGCCTTGACTG | 11060 |
rs770118508 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809901 | GAGTGGGGAAGCTGT[C/G]GTTAACATGGGACAT | 11060 |
rs770120204 | snp | A/C | 1.69172e-05 | 0.00290832 | intron-variant | WWP2 | GRCh38.p7 | 16:69871772 | TTTTCACAGTGACTT[A/C]TGTCTGTCTGCTTTC | 11060 |
rs770125746 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877907 | CCGCCTCCCAGGTTC[A/C]AGCGATTCTCCTGCC | 11060 |
rs770191509 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910757 | GAGGGACGTAGGCCT[C/T]GACCCAGTGAGCATT | 11060 |
rs770192981 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909639 | TCATCATCAGTACTC[A/G]CTGTGTTTTCCACTT | 11060 |
rs770199135 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853652 | CTGACGAAGAGGACT[A/G]TTGCAGGAACTGGTG | 11060 |
rs770206455 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811562 | AGACCAGACTCAGTA[C/T]TGTAGTGAGACACAG | 11060 |
rs770208052 | snp | A/C | 1.67511e-05 | 0.00289401 | missense | WWP2 | GRCh38.p7 | 16:69871858 | AGCAACCGGCGAGCA[A/C]AGCCCCGGTGCTCGG | 11060 |
rs770215392 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887243 | CTACTTTGAGCATGA[A/G]CCTTTACAAGAATGA | 11060 |
rs770215655 | in-del | -/CATT | 3.36005e-05 | 0.00409867 | intron-variant | WWP2 | GRCh38.p7 | 16:69933934 | GTGCACGAAGGGACC[-/CATT]CATTATTCTTGTCTT | 11060 |
rs770245519 | in-del | -/ATTC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806953 | TTTATTTATTTATTT[-/ATTC]ATTCATTCATTCATT | 11060 |
rs770253570 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896490 | GTGTTCCCTGTACCC[A/G]GCATACAACTTGGCT | 11060 |
rs770269846 | snp | A/G | 5.10486e-05 | 0.0050519 | missense | WWP2 | GRCh38.p7 | 16:69888236 | GCCCAGGCCCCCGAC[A/G]CTCTGCCTGCTGGGT | 11060 |
rs770278853 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934150 | GGGGCCCCAGGGGTC[G/T]GCCTAGTTCCCTCCT | 11060 |
rs770283027 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841863 | CATATGATCGTCCCT[G/T]TTCCTCTTCTCCTGG | 11060 |
rs770286512 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | WWP2 | GRCh38.p7 | 16:69930210 | ACTTTGTGGACCACA[A/G]TACCCGCACCACCAC | 11060 |
rs770299956 | snp | A/T | 1.65176e-05 | 0.00287376 | missense | WWP2 | GRCh38.p7 | 16:69787074 | AAGTCTCAGCTCACT[A/T]TGAAAGGTGAGTGGC | 11060 |
rs770306874 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789605 | TGTTTCTTGTGTGTC[G/T]CTTCCAAGATACACC | 11060 |
rs770327300 | snp | C/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942176 | TTGACCTCAGGGTCA[C/T]GTAAGGGCTTGCCAC | 11060 |
rs770343343 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895871 | AGCATCAGATTAAAG[G/T]ATTACACTGAGCGTC | 11060 |
rs770353952 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916653 | GGGAATGATGTTGGC[A/C]TGGTTTCATCCCTGG | 11060 |
rs770369193 | in-del | -/TTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868889 | GTGGTTGACAGCTTT[-/TTG]TTGTTGTTGTTGTTG | 11060 |
rs770372325 | in-del | -/AGAGACGGG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802787 | TTTTTTATTTTTAGT[-/AGAGACGGG]AGTTTCACCATGTTG | 11060 |
rs770374654 | snp | A/G/T | 8.4276e-05 | 0.00649093 | missense | WWP2 | GRCh38.p7 | 16:69888233 | GCTGCCCAGGCCCCC[A/G/T]ACGCTCTGCCTGCTG | 11060 |
rs770375571 | snp | A/G | 1.65236e-05 | 0.00287429 | missense | WWP2 | GRCh38.p7 | 16:69937167 | GAAGAGCAGACCAAA[A/G]CCTTCCTGGATGGCT | 11060 |
rs770384015 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848405 | TGGTGAGCCCAGATC[A/G]TGCCATTGCACTCCA | 11060 |
rs770394965 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776621 | GATCACCTGAGGTCA[C/G]GTGTTCGAGACCAGC | 11060 |
rs770427384 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807424 | ATTGAATTTTTTTTC[C/T]TTCAATGTAGCATTG | 11060 |
rs770431102 | snp | A/C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905649 | TCTAGAGAAGGGGCT[A/C/G]CTCAACCTGTATAAT | 11060 |
rs770437373 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825995 | GAAGCAGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 11060 |
rs770461449 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829803 | GCAGGGACAACGTCT[C/G]TTTCCATTTTCCATG | 11060 |
rs770483572 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829009 | ACCTCCTCAGACTTG[A/G]TCCTGTTCCCGTATT | 11060 |
rs770510776 | in-del | -/GGATGCTGACTGCCGC | 1.6577e-05 | 0.00287893 | intron-variant | WWP2 | GRCh38.p7 | 16:69937521 | GGAGGGACCTGCCGG[-/GGATGCTGACTGCCGC]GGATGCTGACTGCCG | 11060 |
rs770523068 | snp | A/C | 1.70478e-05 | 0.00291952 | intron-variant | WWP2 | GRCh38.p7 | 16:69937671 | GGTCCCGGGCCCAGG[A/C]CTTGGCAGGGACATT | 11060 |
rs770525394 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | WWP2 | GRCh38.p7 | 16:69934011 | AGGTGCTCAACCCTA[C/T]GTATTGTTTATTTGA | 11060 |
rs770527275 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848895 | TCCCAGTGATTTTTT[A/T]ACATGGAAAAGTTTC | 11060 |
rs770533640 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914843 | GTAGAAGTCAAGGCA[C/T]CTTCAGACATTCTGG | 11060 |
rs770542482 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941687 | TTGTTTTGTAATGCC[C/T]GCCCCTTGCCTCGAT | 11060 |
rs770548975 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830641 | AGTGTTGGGGGGCCG[C/T]GGGGAGGTGGAGTAA | 11060 |
rs770555280 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817757 | TTGACCTCCCAGGCT[C/T]AAGTGATCCTCCCAC | 11060 |
rs770575440 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860668 | TTTTGGAGCCTGCCT[C/T]CGTCCTGCTGAATTC | 11060 |
rs770576884 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935747 | TAGTTCTGTCAGGGA[A/G]GGAAGGCGGGTAGCG | 11060 |
rs770593746 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69908777 | TGGGAACAGCGAGAG[C/T]TGCCCAACGGACGTG | 11060 |
rs770597470 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807500 | GGTGTGTGCCTCTGG[C/T]CCCAGCTACTCGGGA | 11060 |
rs770610091 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777545 | ACCTCAAGCAATTCA[C/T]CCACCTCAGCCTCCC | 11060 |
rs770613073 | snp | A/G | 3.30819e-05 | 0.00406692 | missense | WWP2 | GRCh38.p7 | 16:69937578 | ATGCAGGAGATAGAC[A/G]TGAGCGACTGGCAGA | 11060 |
rs770621955 | in-del | -/CCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831826 | TGGAAAAAAACAAAA[-/CCT]TTTTTTTTTTTTTTT | 11060 |
rs770623640 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927115 | ACGATCAGAAAAAAA[A/C]CCACAAAACTGTCAT | 11060 |
rs770636562 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898270 | CAACCTCAGGTGATC[C/T]GCCCACCTCGGCCTC | 11060 |
rs770642573 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806432 | GCTAATTTTATAAAG[G/T]AAATTGATGTGCTTT | 11060 |
rs770645209 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818661 | ACACAATGAATCGAT[C/T]CTTCCTGCTTGACAT | 11060 |
rs770646349 | snp | A/G | 3.29843e-05 | 0.00406092 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931598 | TAGATCATGGTGCCC[A/G]AAACCAGTGGCAGGC | 11060 |
rs770677977 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891313 | TCAGGGGACCAATGA[A/G]AGAAGGAAATCTGTC | 11060 |
rs770679920 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69881219 | CTCCCATTTGGGAAA[C/T]ATCAAAGCTGTCTTC | 11060 |
rs770684268 | snp | A/G | 0.000237598 | 0.0108969 | intron-variant | WWP2 | GRCh38.p7 | 16:69799333 | CGACGTGATTCTTGG[A/G]TGGGGATGGGAGGAC | 11060 |
rs770713707 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825824 | TAGACACAGGATCTC[C/G]CTATGTTGCCCAGGC | 11060 |
rs770724072 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908560 | TTCCATACAGGGGAG[A/C]TATTATAGTTTCTTC | 11060 |
rs770745843 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876525 | ATCTGCTACCACATC[C/T]GGCTAATTTTTGTAT | 11060 |
rs770749820 | snp | A/G | 6.59163e-05 | 0.00574054 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925444 | GTCTTCGAGTGCTTC[A/G]ACTGACCATGATCCC | 11060 |
rs770766124 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890735 | GAGGGTTACTGTTCT[C/T]GGGGATTGGGCACTT | 11060 |
rs770773964 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | WWP2 | GRCh38.p7 | 16:69840152 | CAGCTGACCCTGAAC[A/C]TGCAGACGGAGAACA | 11060 |
rs770786265 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765732 | GGGAGGCTGAGGCAC[A/G]AGAATTGCTTGAGCT | 11060 |
rs770807969 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813351 | ATTTTTAGTGGAGAT[A/G]GGGTTTCTCCATGTT | 11060 |
rs770835960 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875679 | TTTCTTTGCTCATCC[A/G]TAAGACACAACTCCT | 11060 |
rs770839687 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936930 | TGATTTCAAAGACTC[C/T]GGTGTCTGCAGGTCA | 11060 |
rs770880290 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760492 | CGGACCATGCCCGGC[A/G]AATCTTTTTTTTTTT | 11060 |
rs770905522 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920915 | CAGATTCTGGAGCTC[A/C]CATCTGCCTGGTCTT | 11060 |
rs770910169 | snp | A/G | 3.1271e-05 | 0.00395405 | missense | WWP2 | GRCh38.p7 | 16:69939091 | TCACCGGTACCTGCC[A/G]CCTGCCCGTCGGGGG | 11060 |
rs770928774 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827526 | TGTAAAAAAACTCCA[A/G]TGTATACAAGGGAAT | 11060 |
rs770932624 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854808 | CACCTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 11060 |
rs770951249 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907692 | GTACTGATCGGGCTT[A/G]TGTATTATCTCTGAA | 11060 |
rs770953604 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | WWP2 | GRCh38.p7 | 16:69936323 | CCAGAGAGAACAACC[C/T]GGAAGAATGTGGCCT | 11060 |
rs770954085 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931517 | TTTTCAGTCAAATGC[C/T]CTACCTAGCCACGTG | 11060 |
rs770974665 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777040 | TTAAAACAGTATATG[C/T]GTGTGTGTGTATATA | 11060 |
rs770990219 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853229 | TTTAATATGGGGAAT[G/T]AGATGCTTATAAAAG | 11060 |
rs771005989 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844813 | TTACTACGTGTAGCA[G/T]CTGAGTTTTCCCTGG | 11060 |
rs771026172 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779162 | CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTTC | 11060 |
rs771044009 | snp | C/T | 9.89136e-05 | 0.00703186 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931259 | GGGCTCCCGTGGCAG[C/T]TGGGGTTATTGAGTT | 11060 |
rs771045901 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856292 | CAATCTGAAGATGTG[A/G]GGGCATTGGAGGAGG | 11060 |
rs771046902 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868975 | TCACTGCGACCTCCA[C/T]CTCCCGGGTTCTAAG | 11060 |
rs771055082 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760781 | ACTGAGCCTTCATTC[A/G]ACTTGTCCAGAACAT | 11060 |
rs771057404 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894573 | AATTAACTAGCGTGA[A/T]AGAAGCCAACTGGAA | 11060 |
rs771084848 | in-del | -/CACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883408 | ATGTGCGCACACACA[-/CACA]CACACACACACACAC | 11060 |
rs771117318 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800381 | ATTGCAATATTTGGA[A/C]ATATACTTGTGGATA | 11060 |
rs771124264 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873871 | GATTTTCTTTGGTGA[-/T]GGTCCTTGAGTCACT | 11060 |
rs771131242 | in-del | -/GAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889361 | ACAGCAAAGACCTTG[-/GAT]GATAAGAAGACAGCC | 11060 |
rs771177393 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930641 | GAGTTTGAGGCTGCA[A/G]TGAGCTATGATGGCA | 11060 |
rs771291958 | snp | G/T | 3.306e-05 | 0.00406558 | missense | WWP2 | GRCh38.p7 | 16:69936432 | CCGGGTCACAGAGGA[G/T]AACAAGGAAGAGTAC | 11060 |
rs771293405 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791908 | GCTTTTTTGTTGCCT[C/T]TCTTGAAGGTGAATT | 11060 |
rs771328221 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903444 | AAAGTGGAGACTGCT[A/G]ATAAGATGAAAGTTG | 11060 |
rs771329319 | snp | C/T | 1.67256e-05 | 0.0028918 | intron-variant | WWP2 | GRCh38.p7 | 16:69936480 | CGCCGGGGGCTCCGC[C/T]CCAGGGGTGGCGTGG | 11060 |
rs771348015 | snp | C/T | 1.69487e-05 | 0.00291103 | intron-variant | WWP2 | GRCh38.p7 | 16:69871763 | CTTCTGTCCTTTTCA[C/T]AGTGACTTATGTCTG | 11060 |
rs771352727 | snp | A/G/T | 3.30738e-05 | 0.00406645 | missense | WWP2 | GRCh38.p7 | 16:69917845 | CGGAATCAGCTCCAG[A/G/T]GGGCCATGCAGCACT | 11060 |
rs771381011 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792677 | GTGGTAAGAGGTACA[C/T]GACATAACTTATGTA | 11060 |
rs771384183 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924508 | TTTTTGACAACACCC[C/G]CCTTCCCCGCAGGAT | 11060 |
rs771387463 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811784 | TCAAATTCAGAGAAG[G/T]GTTACAAGAATAGAA | 11060 |
rs771393098 | in-del | -/CTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831826 | GGAAAAAAACAAAAC[-/CTT]CTTTTTTTTTTTTTT | 11060 |
rs771426173 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902915 | TGAATAGCCATGCAG[G/T]TGAGGGAGGAGTGAG | 11060 |
rs771455603 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798133 | TCTCCTGTAGCACTG[A/G]TGGGAGGCTACATGG | 11060 |
rs771456258 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768401 | ATCACCTGAAGTCAG[G/T]AGTTTAAGACCAGCC | 11060 |
rs771460577 | snp | G/T | 1.67503e-05 | 0.00289393 | intron-variant | WWP2 | GRCh38.p7 | 16:69929572 | GGGCTGGGCTGGGTC[G/T]CTGTGCAGCTCCAGC | 11060 |
rs771484500 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906629 | GGCACGTTGGTTTGT[A/G]ATACCAGCACTTTGA | 11060 |
rs771486048 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887369 | AAAGGATGTGACCCT[A/G]TAAACTTGGCCTTGC | 11060 |
rs771491129 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797258 | AGCGGAAGAAGAAAT[A/G]TAGATGACTAACGAC | 11060 |
rs771541812 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934882 | CAGAGAGGGCGCGCC[A/G]GTCCATGGGCGCTGC | 11060 |
rs771568033 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816064 | CAGCTACAGACCCTG[C/G]TGCCTTCAACAGGCT | 11060 |
rs771569190 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831827 | GGAAAAAAACAAAAC[-/C]TTTTTTTTTTTTTTT | 11060 |
rs771571733 | snp | A/G | 1.65499e-05 | 0.00287657 | missense | WWP2 | GRCh38.p7 | 16:69937551 | GCCTCTCCCCAGCTG[A/G]TGCTGTGCGGCATGC | 11060 |
rs771577704 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896565 | TCACATTCTCAGTGG[C/T]CCTTAAAATTTTTTA | 11060 |
rs771603969 | snp | A/G | 0.000132773 | 0.0081467 | intron-variant | WWP2 | GRCh38.p7 | 16:69939820 | CTAGGGCTGACTGTC[A/G]TGCTTCCCCACTCTC | 11060 |
rs771611815 | snp | C/T | 4.57844e-05 | 0.00478436 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933160 | CACAGGGTAGAACCA[C/T]GGACAGGATACCGGG | 11060 |
rs771612282 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840570 | ATGTGACTTTGGCCC[A/G]TTATTTTCCTTCCCA | 11060 |
rs771631621 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889148 | TGATATCCTGCCTAC[-/AC]ACACACACACACACA | 11060 |
rs771634782 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810055 | GTGGCCTAGTCTTCC[C/T]GCAGCATCTTTTCCT | 11060 |
rs771693204 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933589 | TTATTGTAATAAACA[C/T]GCATCGTGCCCTTGT | 11060 |
rs771703869 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841782 | CTTGGATGTTCTTCA[A/G]TGTCTTGGAGAAGAG | 11060 |
rs771705520 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906314 | CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC | 11060 |
rs771708494 | snp | A/G | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925017 | GTGGTTCTTGGAGAA[A/G]GTTGGAGGTGGTGGT | 11060 |
rs771718624 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890753 | GGATTGGGCACTTCC[A/T]GTTTCCAGGCAGCTG | 11060 |
rs771762629 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789503 | AAAGTGCTGGGATTA[C/T]GGGCGTGAGCCACCG | 11060 |
rs771788124 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774485 | TGGTCTCGAACTCCT[A/G]GATTCAAGTGATCCA | 11060 |
rs771789461 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817367 | GATTCTCCCATCTTA[G/T]CCTCCCGAATAGTTG | 11060 |
rs771790030 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829621 | TTAGATGACAGTTAT[C/T]AGTTTCTCAAGAAAC | 11060 |
rs771795335 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916899 | CCGGGTGCAGTGGCT[C/G]ACGCCTGTAATCTCA | 11060 |
rs771828939 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871239 | CAATGAGCTATGATC[A/G]TGCCACTCCAGCCTG | 11060 |
rs771857198 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775419 | AAGGTATCTTAAACC[C/G]CATCAGCCATGTCCT | 11060 |
rs771868406 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901344 | CAGTGTATTCTTCTT[A/C]AGTTTAATTTTTGTC | 11060 |
rs771874836 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865001 | TTATGATGTTGAGCA[A/T]CTTTTTTTGTGCTTA | 11060 |
rs771879171 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804494 | TCAGCTTATATTAAA[A/T]ACATATGTGTATTTG | 11060 |
rs771883660 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763382 | CTTGTGTTAAAGCCT[A/G]TTCATCTTCCTGTTT | 11060 |
rs771891311 | snp | A/G | 1.68684e-05 | 0.00290412 | intron-variant | WWP2 | GRCh38.p7 | 16:69917894 | ACCAGGTGAGAGGGC[A/G]GGCGCTTGGCCCGAG | 11060 |
rs771912658 | snp | A/C | 1.65425e-05 | 0.00287593 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931506 | TTCTTTTTTTTTTTT[A/C]AGTCAAATGCCCTAC | 11060 |
rs771918775 | snp | C/G | 0.00309951 | 0.0392447 | missense | WWP2 | GRCh38.p7 | 16:69799215 | ATTTAAAGGTCTGGA[C/G]CTGCCATACCTTGAG | 11060 |
rs771920744 | snp | C/G | 1.67668e-05 | 0.00289537 | missense | WWP2 | GRCh38.p7 | 16:69888228 | CAGCGGCTGCCCAGG[C/G]CCCCGACGCTCTGCC | 11060 |
rs771925371 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794107 | ACTTGTAGTAGAGAC[A/G]GGGTTTCACCAAGTT | 11060 |
rs771934628 | in-del | -/TA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914911 | AGCTACTCCATGATT[-/TA]TCGCACCAAATCCCA | 11060 |
rs771945141 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776555 | TGATAATAGGCCGGG[C/T]GCAGTGGCTTACGCC | 11060 |
rs772006112 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890816 | CTAAGTCTGGCAGAT[C/T]GAGCAGCCCAGGGAA | 11060 |
rs772043997 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909376 | TAGCCATGAAGGGCT[C/T]CTGTATAAAATATGC | 11060 |
rs772048213 | in-del | -/T | 4.14508e-05 | 0.00455233 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939954 | AACCGAGGCCGCCCC[-/T]CCCACGCCCCCCAGC | 11060 |
rs772068560 | snp | C/T | 6.88634e-05 | 0.00586745 | intron-variant | WWP2 | GRCh38.p7 | 16:69871950 | AGTGATGGCACCGCA[C/T]GCCAGCCTGCACTGA | 11060 |
rs772085607 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837629 | TCTCCTGTTGAACAT[C/T]ATCAGTCCTCCAGGA | 11060 |
rs772092470 | snp | A/C | 1.66098e-05 | 0.00288177 | intron-variant | WWP2 | GRCh38.p7 | 16:69935994 | TGGATCAAGTGAGTT[A/C]CCTGCCCCCTTGCCC | 11060 |
rs772094095 | snp | A/G | 4.03071e-05 | 0.00448909 | intron-variant | WWP2 | GRCh38.p7 | 16:69939138 | GGTATGTTTTCTCTC[A/G]CCCTCTGGCGTCCTG | 11060 |
rs772098857 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834347 | GTTCTTCCTCCAGAT[A/G]CCCACGTGACTTCCC | 11060 |
rs772101164 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783629 | CAAATAGAATGACAG[A/G]AGGTATTAATGATGT | 11060 |
rs772108211 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69865896 | TGCCGGTCAGTTGCT[C/G]TGTGGAAACCACAAA | 11060 |
rs772124618 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876769 | GAAAACAACATTAAT[A/C]TCCTTGTAAATCTCC | 11060 |
rs772136022 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69847404 | TATTTATTTTTCTTA[-/T]TTTTTTTTTTTTTAA | 11060 |
rs772140489 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856241 | ATTCCATTTATATAA[C/T]ATCCTGGAAAAGGCA | 11060 |
rs772150301 | snp | A/T | 1.65353e-05 | 0.00287531 | stop-gained, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931814 | CAGATCATGAACATG[A/T]AACCCTATGACCTGC | 11060 |
rs772152932 | snp | C/G | 1.65614e-05 | 0.00287757 | intron-variant | WWP2 | GRCh38.p7 | 16:69798834 | ATCATCATTTTGTAA[C/G]AGAAAGCCCCTTCTT | 11060 |
rs772153969 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937041 | GGTCCTGCGCGGTAA[C/T]GGCCACGCGGCCTGG | 11060 |
rs772177832 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825551 | ATTTTTTTGATGAGC[A/G]CATTATTTTTTATTT | 11060 |
rs772180549 | snp | C/T | 3.33261e-05 | 0.0040819 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935876 | CCATGGAAAGTTCAT[C/T]GACACGGGCTTCACC | 11060 |
rs772183729 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781156 | AAAGAACTGAGATGG[A/G]AGTCTGTCTGCACGT | 11060 |
rs772202119 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854739 | TATTTTTAGTAGAGG[C/T]GAGGTTTCGCCAAGT | 11060 |
rs772207873 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800318 | GTGTTTATTTTCCCA[A/G]ACCCTAGCCAGCCTT | 11060 |
rs772231112 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69770423 | CTTCTGGATGGCTGC[A/C]CACGTGGAGGTTCTT | 11060 |
rs772233918 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843245 | GTAATGTTGGTTAAG[A/T]CCTCCTACGCTTAGA | 11060 |
rs772253222 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777143 | TGGATATATATACAC[-/AT]ATGTGTATATACAAT | 11060 |
rs772297725 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790759 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTTGC | 11060 |
rs772299867 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941347 | CGGGTGCCTTCCAAG[C/T]ACAGTCTCCATGCTC | 11060 |
rs772309780 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919698 | TTTTCTCAGAGCACT[C/T]TAGATGCGAAGGTTG | 11060 |
rs772316286 | snp | A/C | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69762014 | TATCTGGCAACCCTA[A/C]TAAAGGAGCTCAATT | 11060 |
rs772322100 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830778 | AGAGCCATCGTAACA[A/G]TAAATCCTGGAATCA | 11060 |
rs772347162 | snp | A/G | 1.69573e-05 | 0.00291177 | intron-variant | WWP2 | GRCh38.p7 | 16:69840312 | GGACAGGGTGGGGCT[A/G]GGCGGGGGCCAGGAG | 11060 |
rs772354073 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813240 | CGATCTTCGCTCACC[A/G]CAACCTCCGCCTCCT | 11060 |
rs772356174 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802324 | GTTAAGTACATTCAC[C/G]TTGTACAACCATCAC | 11060 |
rs772395854 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895440 | CGAATCTATTGAGCA[C/T]ACATGTGGATATTAC | 11060 |
rs772397704 | snp | C/T | 9.90262e-05 | 0.00703586 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939399 | GGAAACCTGGCTGCC[C/T]AGAAGCCACACCTGG | 11060 |
rs772412036 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903494 | AGAAAAATGGCCGGG[C/T]GCAGTGGCTCACACC | 11060 |
rs772415160 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831504 | ATGCCCTATTTATCT[A/G]TATTTATTAGTACCA | 11060 |
rs772419445 | in-del | -/AC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884770 | ATTCTGAAGACTGGT[-/AC]AAACAAAGGGAAAGA | 11060 |
rs772444842 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906880 | CAAGACTCTGTCTTT[-/A]AAAAAAATAAAAAGA | 11060 |
rs772485253 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894696 | CAATGGGAAGCGAGG[C/G]TGCTTTGGTCTGCAG | 11060 |
rs772486443 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778535 | CTTCTTGTAGTGGAT[A/G]GTGGGGATTTGGACC | 11060 |
rs772493060 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912101 | GAGACCATCCTGGCT[A/C]ACACGGTGAAACCCC | 11060 |
rs772493913 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904735 | TAAAATACTAAATGA[A/C]ATATGAAGATCTCCC | 11060 |
rs772514474 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | WWP2 | GRCh38.p7 | 16:69917759 | ACTATGTGGATCACA[A/G]TACTCGGACCACCAC | 11060 |
rs772519701 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814263 | ACTCCTGGGCTCAAG[C/T]GATCCTCTTGCCTCA | 11060 |
rs772543816 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879946 | AATGTGTATAATTTC[A/G]GTTTTTGCGTCAATA | 11060 |
rs772563519 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819589 | ATTTAATTTAATTTT[A/C]TAGAGATGGGATCTC | 11060 |
rs772579582 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861219 | AGCCATCAATGGCCA[C/T]GTTGAGCAGGTGAAC | 11060 |
rs772603134 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926846 | GGCAGGGGAAAATGC[A/G]TCAGATTAAACAAGA | 11060 |
rs772641079 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779252 | CACTGTGCGTGGCCC[C/T]GGCCGGTTATTTTTC | 11060 |
rs772655319 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807857 | CCAGCTACTTGAGAG[G/T]CAGTGGTGGGAGGAT | 11060 |
rs772662673 | snp | A/G | 4.59823e-05 | 0.00479469 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933161 | ACAGGGTAGAACCAC[A/G]GACAGGATACCGGGG | 11060 |
rs772668081 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902175 | GAAACCTTTGACAAG[-/A]AAACATGGTTCAGGA | 11060 |
rs772669307 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862164 | TCAGCCTCCAGGGTT[C/G]AAGTGATTCTCTTGC | 11060 |
rs772674509 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904894 | ATAAGTAAGCAAGAG[A/G]CCGTTAGCCTGAAGC | 11060 |
rs772711584 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817438 | ATTTTTAGTAGAGAC[A/G]GGGTTTTTGCTATGT | 11060 |
rs772738114 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789016 | ATGCAAATGTTATTT[A/G]TATAATATACTCATG | 11060 |
rs772753506 | snp | C/T | 1.6549e-05 | 0.0028765 | intron-variant | WWP2 | GRCh38.p7 | 16:69933962 | CTTTTCTGTCTCTTC[C/T]CTCACAGAGAGTGGT | 11060 |
rs772781669 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828883 | GGTGAGCCACAGATT[G/T]GAATCACTTCTGAGC | 11060 |
rs772790067 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941566 | GAGGTTTGGAAGCAT[C/T]AGGCTCACGGGTGTT | 11060 |
rs772799446 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804541 | TTCCATTGAATCCAT[C/T]GTTTTATTAGCCTTT | 11060 |
rs772802727 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816095 | TCATGGTAGAAACTG[C/G]TAACCCAGTCCTGCA | 11060 |
rs772808451 | in-del | -/GC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848164 | GAAGCTGTCAGCTGG[-/GC]GCGCAGTGGCTCAGC | 11060 |
rs772817827 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834777 | AAATGATCCGCCTGC[C/T]TTGGCCTCTGAAAGT | 11060 |
rs772827651 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69866253 | CCACAAAATGCTTTT[A/T]AAAAAAAGGTTTCAC | 11060 |
rs772836351 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936108 | TCTTTTCCAGCCTCT[A/G]TAAGAGCTTGTGGAG | 11060 |
rs772845306 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774363 | CAGGCTCAAGCGATC[A/C]TCCCACCTCACCTCA | 11060 |
rs772851577 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940119 | CCCTGCAGTTCCCCC[A/G]ACCCGCGGATGGCAG | 11060 |
rs772869666 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829741 | CAACTTTACATTTCC[A/T]TGTTACTTCCACTTC | 11060 |
rs772889691 | in-del | -/GA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831685 | AGGAAAAATAAGAGT[-/GA]GAGTTATTCCCCAAA | 11060 |
rs772896883 | in-del | -/G | 3.43133e-05 | 0.00414191 | intron-variant | WWP2 | GRCh38.p7 | 16:69917669 | TTGGGGGATGGGAGT[-/G]GGGTGGTCATTATAT | 11060 |
rs772904948 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69822332 | TCGTGCAGTAAGCAC[C/T]TTTGAATTCCGAGCT | 11060 |
rs772941934 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775456 | TGATGAGCCCATCAA[A/G]GCATTCTTCACTTCT | 11060 |
rs772951367 | snp | A/G/T | 6.60615e-05 | 0.00574691 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937199 | CAACGAGGTGGCCCC[A/G/T]CTGGAGTGGCTGCGC | 11060 |
rs772965043 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903847 | AACAGATATTTTGTC[-/TT]TATAAAAGGGGCAGC | 11060 |
rs772996364 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794120 | ACGGGGTTTCACCAA[C/G]TTGGCCAGGCTGGTT | 11060 |
rs773005230 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | WWP2 | GRCh38.p7 | 16:69799233 | GCCATACCTTGAGAA[A/G]TGAACTGCTAGGCAC | 11060 |
rs773016456 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826267 | AGTGAAACTCCGTCT[-/CA]AAAAAAAAAAAAAAG | 11060 |
rs773027951 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855763 | AGGAACAGTGGAGAG[C/G]CCAGTCCCACTGGAG | 11060 |
rs773040242 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906865 | AGCTCGGGCAACAGA[A/G]CAAGACTCTGTCTTT | 11060 |
rs773061673 | snp | A/G | 5.08255e-05 | 0.00504085 | intron-variant | WWP2 | GRCh38.p7 | 16:69917898 | GGTGAGAGGGCAGGC[A/G]CTTGGCCCGAGGTGG | 11060 |
rs773074583 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810427 | CAGTTTTTTAACATC[-/T]TTTTTTTTTTTTTTT | 11060 |
rs773080360 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874157 | AGGGCTTGATGTCCA[A/T]CTCTCCCCTTTCTGC | 11060 |
rs773086201 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795260 | AAAAAAAATGCGGAT[A/G]CACACACACACACAC | 11060 |
rs773086325 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782292 | CATCTCAAACAAACA[A/G]ACAGACAAACAGAGG | 11060 |
rs773100932 | snp | A/G | 3.37735e-05 | 0.00410921 | intron-variant | WWP2 | GRCh38.p7 | 16:69799322 | GAAGGGGGTGCCGAC[A/G]TGATTCTTGGGTGGG | 11060 |
rs773110589 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909641 | ATCATCAGTACTCAC[C/T]GTGTTTTCCACTTTG | 11060 |
rs773115489 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888410 | AAGAACTGCTTGTTC[C/T]ACATAAATCTTAAAA | 11060 |
rs773117705 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898467 | TGCATAAGCATTCCT[G/T]CTAAAACTTAGTGTT | 11060 |
rs773130140 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918110 | AAGGAATCAACGTGT[C/T]TAAAACTGAATTCCC | 11060 |
rs773131958 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781238 | GATGAGGGTGGGGGG[-/A]TACTGGGGAGCAGGA | 11060 |
rs773149907 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925434 | CTTGTGTTTAGTCTT[C/T]GAGTGCTTCGACTGA | 11060 |
rs773150825 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893331 | TAGGCTCCCAAGACA[C/T]GTTTGCAATGAATGG | 11060 |
rs773170056 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69872781 | AGACAGTGCCGTCCA[C/T]GTGCGCATGGAACTT | 11060 |
rs773172044 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883954 | GTGGTCAGCTATTTC[A/G]TAATAATTATTTTTA | 11060 |
rs773176195 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783640 | ACAGAAGGTATTAAT[G/T]ATGTTGAATAGAACA | 11060 |
rs773179648 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823416 | TGGGAAACTTCTCTT[A/C]TTTTATTTATTTATT | 11060 |
rs773192064 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800645 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCCAGG | 11060 |
rs773205333 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897552 | TTTAAACTGCTATAC[A/G]GTGTTCTGTTACATG | 11060 |
rs773216988 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798269 | TAATTTCCCCAGAGC[A/G]AACAATTGCAAGCAG | 11060 |
rs773218849 | snp | C/T | 3.37012e-05 | 0.00410481 | missense | WWP2 | GRCh38.p7 | 16:69871806 | TTTGAACCCCCAGGA[C/T]GCACAGACATTCGGG | 11060 |
rs773222084 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826726 | CTAATAAAAATACAA[-/A]AAAAAAAAAAAAAAT | 11060 |
rs773235587 | snp | A/G/T | 6.59395e-05 | 0.00574161 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69798746 | CTACGTGGAGGTGGC[A/G/T]GTGGATGGACTCCCC | 11060 |
rs773249235 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769621 | CAGAGCCAAGAATTT[C/T]AGTATCGAGAAGTGG | 11060 |
rs773263909 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882950 | TTGAGGTCAGGAGTT[A/C]CAGACCAGCCTGGCC | 11060 |
rs773285649 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880411 | AAGAGCTAGTTTTGC[A/C]TTTTTTTCCTCCATG | 11060 |
rs773291424 | in-del | -/A | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940585 | GGGTATCCACGGGAC[-/A]AAAACAGCAAACTCC | 11060 |
rs773298119 | snp | C/T | 1.66139e-05 | 0.00288213 | intron-variant | WWP2 | GRCh38.p7 | 16:69935996 | GATCAAGTGAGTTCC[C/T]TGCCCCCTTGCCCCA | 11060 |
rs773300139 | snp | C/G | 4.94197e-05 | 0.00497066 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931167 | GACGAAGCAAGGTTC[C/G]CCTGGTGCTTATGAC | 11060 |
rs773309509 | in-del | -/TTTTTTTTTTTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817661 | TTTTTGTTAAACTCT[-/TTTTTTTTTTTT]TTTTTTTTTTTTTAA | 11060 |
rs773310574 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873545 | CACTGTATCCTTGTG[C/T]TGGAACATCCGGTGG | 11060 |
rs773344802 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789226 | CCAGGCCTGGCTAAC[-/TT]TTTTGTTTGTTTGTT | 11060 |
rs773352487 | snp | A/C/T | 6.61402e-05 | 0.00575033 | missense, synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931826 | ATGAAACCCTATGAC[A/C/T]TGCGCCGCCGGCTCT | 11060 |
rs773363899 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783393 | GATAAGTCAGGCACC[-/G]GGCTTGGTGGTCCGA | 11060 |
rs773370772 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894397 | CATTGTCTTTTTGAA[A/G]TATGCAGCAGATGAG | 11060 |
rs773383475 | snp | A/G | 5.76784e-05 | 0.00536991 | intron-variant | WWP2 | GRCh38.p7 | 16:69938978 | ACGTTCGGGCAAAGT[A/G]CTGGGCCCCGTGGGT | 11060 |
rs773401510 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830803 | GAATCATCTGGCTTC[C/T]TTTACTGCAAAGGAA | 11060 |
rs773413103 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | WWP2 | GRCh38.p7 | 16:69917764 | GTGGATCACAATACT[C/T]GGACCACCACCTGGC | 11060 |
rs773414786 | snp | C/T | 3.29701e-05 | 0.00406005 | missense | WWP2 | GRCh38.p7 | 16:69936425 | AGAGCATCCGGGTCA[C/T]AGAGGAGAACAAGGA | 11060 |
rs773416819 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902055 | TTGGTGAAATGTTGA[C/T]TTGGTTCAAACAGGT | 11060 |
rs773420110 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929749 | TGGTGGATGGAGGGC[A/G]GCCCGGCTGGCGGGT | 11060 |
rs773420173 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939254 | TCTGCATCCTGGGGC[C/T]GAGCCCATCTGTGGG | 11060 |
rs773441037 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813332 | CACACCCAGCTAATT[A/T]TATATTTTTAGTGGA | 11060 |
rs773441857 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939719 | TGAAGGCCTGACTGG[-/C]CAGCCCCTGAGCCCT | 11060 |
rs773442574 | snp | A/C | 1.65836e-05 | 0.0028795 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931751 | TCCCTCCCGCCCCTG[A/C]CTGCTGTGGAAGGGA | 11060 |
rs773445578 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791827 | GCCTGGCCCCCACCT[C/T]GGCCTCTTAAGGTGC | 11060 |
rs773464348 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844118 | GATGCCATTTCCCCA[C/T]TCTCTTTTCTCCAAG | 11060 |
rs773489462 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818788 | CCCAGTCTGCAAACA[C/T]GGGGGTGCTCCATGG | 11060 |
rs773503057 | snp | A/T | 1.65348e-05 | 0.00287526 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908900 | AACTGACACCATGAG[A/T]CACCCAATGGCTTCT | 11060 |
rs773506844 | snp | G/T | 2.28569e-05 | 0.00338052 | intron-variant | WWP2 | GRCh38.p7 | 16:69939817 | CTCCTAGGGCTGACT[G/T]TCGTGCTTCCCCACT | 11060 |
rs773508065 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938418 | AGGTCAGGAGTTCAA[G/T]ACCAGCCTGGCCAAA | 11060 |
rs773528912 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800321 | TTTATTTTCCCAAAC[C/G]CTAGCCAGCCTTTTG | 11060 |
rs773607792 | in-del | -/TC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762581 | GCTCCCGCCCGAGTG[-/TC]GGGTGGGCGCGCCGC | 11060 |
rs773617409 | snp | A/G | 3.30098e-05 | 0.00406249 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929480 | GGACGGGTGTATTAC[A/G]TGAACCATAACACTC | 11060 |
rs773632685 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863475 | GAAACCCCGTCTTTA[C/T]TAAAAACACAAAAAT | 11060 |
rs773652220 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796338 | CAAGTTGAAAATGCA[C/T]CTGATACTCCTAATC | 11060 |
rs773682328 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69910938 | CGCCCTGCATAGCTT[A/G]CTAGTCCTTCCTGAG | 11060 |
rs773683409 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | WWP2 | GRCh38.p7 | 16:69936361 | TACTTCATCCAGGAC[A/G]TGGAGATACTGGGCA | 11060 |
rs773703944 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776763 | AACCTGGGAGGCGGA[A/G]GTTGTGGTGAGCCGA | 11060 |
rs773770913 | snp | A/G | 0.000132536 | 0.00813943 | missense | WWP2 | GRCh38.p7 | 16:69939401 | AAACCTGGCTGCCCA[A/G]AAGCCACACCTGGTG | 11060 |
rs773771915 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924392 | CTTGATCCCCTCTTA[C/T]AACGATTAAATTTTA | 11060 |
rs773773971 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909669 | TTGACTTGAAGTCAA[A/G]TGAAGTTACCAAAGT | 11060 |
rs773779758 | in-del | -/TTCT | 5.07142e-05 | 0.00503533 | intron-variant | WWP2 | GRCh38.p7 | 16:69929423 | TGTTTGAATCTGATG[-/TTCT]TTCTTTCTTCTCATG | 11060 |
rs773789065 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | WWP2 | GRCh38.p7 | 16:69937197 | TTCAACGAGGTGGCC[C/T]CGCTGGAGTGGCTGC | 11060 |
rs773797549 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886725 | AGATGGCGCCATTCC[A/C]CTCCAGCTTGGGTGA | 11060 |
rs773828106 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808945 | CCTTTAGTAGACACC[A/G]TCAGTTTTCTAGTGT | 11060 |
rs773848301 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885142 | ACACACACACACACA[-/TT]CTTCTTCTTTAGAAT | 11060 |
rs773864081 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922959 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 11060 |
rs773879544 | snp | C/G | 3.35469e-05 | 0.0040954 | intron-variant | WWP2 | GRCh38.p7 | 16:69937289 | GCCTCTGGGGCGATC[C/G]TGCTCTGTGATACGC | 11060 |
rs773903470 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931250 | CTGGTACTGGGGCTC[C/T]CGTGGCAGTTGGGGT | 11060 |
rs773906271 | in-del | -/GGAAACG | 3.57564e-05 | 0.00422811 | intron-variant | WWP2 | GRCh38.p7 | 16:69937703 | GGGCCATCAACCAAA[-/GGAAACG]GGTCCTGAGGAGGCC | 11060 |
rs773916764 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905689 | GTCATCTTGATCCTA[A/C]CTCAATGCCAGTGCT | 11060 |
rs773918117 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797182 | GTAGCTTTGTACTCC[A/C]TGAGTCTTTGGCTTG | 11060 |
rs773936579 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827855 | CTGATAATTTATTCT[A/G]AAGACTTAACCTTCC | 11060 |
rs773954634 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69814929 | AGAGAAGAAATTTTT[A/T]AAAAGTTGCTCTTCA | 11060 |
rs773960623 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845066 | CAGGAGATGCAGATC[A/G]AATCCTGGCCTGTCA | 11060 |
rs773966457 | snp | A/T | 1.72698e-05 | 0.00293847 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931931 | GCCCTGTACCCCGCT[A/T]CCCCAGGCTACAGCA | 11060 |
rs773981032 | snp | A/G | 1.66496e-05 | 0.00288522 | intron-variant | WWP2 | GRCh38.p7 | 16:69798863 | TTTTTGAACGCAGCA[A/G]GATGGGGAAAGAGAG | 11060 |
rs774006580 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785297 | GGAAGGGGAGCGGAT[A/G]TGAGTTTTTAAGTGA | 11060 |
rs774009817 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761342 | CTTTGGGAGGCCAAG[A/G]TGGGCGGATCATTTG | 11060 |
rs774013326 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922929 | GAGTCTCGCTCTGTT[A/G]CCCAGGTTAGAGTGC | 11060 |
rs774021191 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840397 | GGCCCATAGCTAGCC[C/T]GGACTCTTCTTAGCT | 11060 |
rs774026712 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823946 | TGTTTCTCATCAGCC[A/G]TGTAGCATTCAGGCC | 11060 |
rs774073903 | snp | A/G | 4.95176e-05 | 0.00497558 | synonymous-codon, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929473 | GGACAATGGACGGGT[A/G]TATTACGTGAACCAT | 11060 |
rs774102629 | snp | C/T | 0.00041307 | 0.0143654 | splice-donor-variant | WWP2 | GRCh38.p7 | 16:69787082 | GCTCACTTTGAAAGG[C/T]GAGTGGCACTGTATA | 11060 |
rs774134998 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803390 | ACATTATCTTACACA[A/G]TTACTGTATCGTTAT | 11060 |
rs774138710 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804790 | TAATGGGGAATTTTC[A/T]TACTGAACTCCCCAC | 11060 |
rs774150015 | snp | A/G | 1.92777e-05 | 0.00310459 | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69939943 | TGGACAGGAGTAACC[A/G]AGGCCGCCCCTCCCA | 11060 |
rs774156610 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914970 | GGGATGCAAGACACA[A/G]GGAACTTAACCCCGA | 11060 |
rs774181341 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837050 | CACCTCTGCCTCCTC[A/G]GTATCTGGGACTACA | 11060 |
rs774194448 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772169 | TTTCATCATGTTGGT[C/T]AGGCTGGTCTCGAAC | 11060 |
rs774233150 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804413 | TTTTTTTCCCTAATA[C/T]GTAGCTGATTGGTTT | 11060 |
rs774238123 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761057 | GCAGAGGTTGCAGTG[A/G]GCCAAGATTGAGCCA | 11060 |
rs774246959 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864987 | ACTTCCCGAAGAACT[G/T]ATGATGTTGAGCATC | 11060 |
rs774251870 | snp | C/T | 1.65181e-05 | 0.00287381 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799210 | TTTAGATTTAAAGGT[C/T]TGGAGCTGCCATACC | 11060 |
rs774265053 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907741 | TTCTTTCAGTAGTGC[A/G]CATAAGCCATCCTCA | 11060 |
rs774266822 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890739 | GTTACTGTTCTCGGG[C/G]ATTGGGCACTTCCTG | 11060 |
rs774276961 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69775273 | AGGGTCATATGACCC[A/G]TTTCAGGGGAAGGTC | 11060 |
rs774277256 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787292 | TAGCTAAAATTGTCT[-/A]AAAATGGTGATTTCA | 11060 |
rs774286440 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763036 | GAGATTTTCCCTGAA[C/T]GGGCCATCATCGAGG | 11060 |
rs774294057 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69782144 | AGAAATTAGCTGGGC[A/G]TGTTAGCGGGTGCCT | 11060 |
rs774344920 | snp | C/T | 8.29993e-05 | 0.00644149 | intron-variant | WWP2 | GRCh38.p7 | 16:69787116 | TCTTCATCTTGTCTA[C/T]GCCCAGGGAAGAGGG | 11060 |
rs774350006 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863739 | GCTCCTCCTTGTACC[C/T]GTCGCTGCTGGCAAG | 11060 |
rs774354576 | snp | A/G | 1.69622e-05 | 0.00291219 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935858 | TCCTTCCCAGGCGCT[A/G]TACCATGGAAAGTTC | 11060 |
rs774367312 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769392 | GCTCTGCCTGTTTCT[A/G]CAGCTGGTTAATTAG | 11060 |
rs774368555 | snp | C/T | 3.29804e-05 | 0.00406068 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917790 | CTGGCAGCGTCCGAC[C/T]GCGGAGTACGTGCGC | 11060 |
rs774402909 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69874453 | TTATTTAGCAGCCTT[C/T]TTTGGCTGCGCACTG | 11060 |
rs774410040 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784092 | TTCTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs774442311 | snp | A/C | 1.65031e-05 | 0.00287251 | intron-variant | WWP2 | GRCh38.p7 | 16:69934141 | CATGGTAAGGGGGCC[A/C]CAGGGGTCTGCCTAG | 11060 |
rs774455983 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853771 | TGGCTGGCTAATGAG[A/G]CAAGGTGAAGGGTAA | 11060 |
rs774457002 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860149 | AGACCCCCATCGCTA[-/T]TAAAAAAAAATCAAA | 11060 |
rs774473596 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919615 | CCACAGTGAGCTGGA[A/G]GTGGGGAAGCCCAGC | 11060 |
rs774475918 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778075 | AACCCTGTCTCAAAT[-/AT]ATATATATATATATA | 11060 |
rs774484607 | in-del | -/AT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870897 | CTCTGAAGATGTCTG[-/AT]AGGTTTTCTGCTGCT | 11060 |
rs774515888 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935563 | CAGGAGCCAGCCGGC[C/T]AGCGTGCGGGGCAGA | 11060 |
rs774523416 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780869 | ATAAATTAATAAAAA[-/AG]GAAAAAAATCAGCTG | 11060 |
rs774543280 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854614 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 11060 |
rs774545413 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842127 | AAGATCCCGGTAAGA[A/C]CCCCCTTGGTGAGGA | 11060 |
rs774550126 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69892555 | TTTTCTTTTTTTGAG[A/G]CATTGTCTTACTCTG | 11060 |
rs774557900 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931540 | GCCACGTGAAGATCA[A/G]CGTTTCCAGGCAGAC | 11060 |
rs774565505 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853280 | ATAGGAGTGAGGGGT[C/T]TCCCTGAGGTCTTTG | 11060 |
rs774571665 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | WWP2 | GRCh38.p7 | 16:69936332 | ACAACCTGGAAGAAT[A/G]TGGCCTGGAGCTGTA | 11060 |
rs774576767 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867928 | CCCTGCATTTGTCTG[C/G]GTGCTATTTTGGCCC | 11060 |
rs774587735 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823158 | AGTAAAAACAAAAAC[A/G]CAGGTGAAATTAATT | 11060 |
rs774624062 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920259 | GTTTGTCTTAGTAAG[A/T]TGCTCCAGGGTCGAC | 11060 |
rs774635245 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843184 | ATGGTTCTTTGTGCA[A/G]TTTTCTGTCATGCAT | 11060 |
rs774635737 | snp | G/T | 1.64893e-05 | 0.0028713 | missense | WWP2 | GRCh38.p7 | 16:69798729 | CAACCTCGAATTAAC[G/T]CCTACGTGGAGGTGG | 11060 |
rs774653393 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930690 | GGTGACAGAGTGAGT[C/T]CCTGTTTCTAAAAAA | 11060 |
rs774661579 | snp | C/G | 1.65012e-05 | 0.00287234 | missense | WWP2 | GRCh38.p7 | 16:69939392 | TTGGCAAGGAAACCT[C/G]GCTGCCCAGAAGCCA | 11060 |
rs774687229 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818746 | CTGGTCACTCTCATT[C/T]AGTCTCCCTTGCTCG | 11060 |
rs774696446 | snp | G/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940253 | GGTGTATGTGAGTGT[G/T]CAAGGGAAGGTGTTG | 11060 |
rs774715755 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849015 | TTGCCTTGGCATTAA[C/T]GGCCTCTGAAGATTT | 11060 |
rs774748100 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | WWP2 | GRCh38.p7 | 16:69908796 | CCAACGGACGTGTCT[A/G]TTATGTTGACCACAA | 11060 |
rs774749651 | snp | C/G | 0.000137953 | 0.00830407 | intron-variant | WWP2 | GRCh38.p7 | 16:69939168 | GGCTGGCAGTGCGGA[C/G]AGCTCAGAGGGAGGG | 11060 |
rs774778493 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790723 | TGGGTTTACAGGCAT[A/G]TGCCACCACACCTGG | 11060 |
rs774786242 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938785 | GGGAAGAGAATACCC[A/C]GCCTGAGGTGTCCCT | 11060 |
rs774874135 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878055 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 11060 |
rs774899973 | snp | C/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942135 | AGGTTTCACAAGTTC[C/T]ACGACGGTCGAGGGA | 11060 |
rs774904623 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860185 | TAGCCAGGCGTGGTG[G/T]TCCGATTCCATTCTT | 11060 |
rs774921551 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69807293 | ACCTGCCTCAGTCTC[C/G]CATACTGCCGGGATT | 11060 |
rs774942338 | snp | A/G | 4.37072e-05 | 0.00467458 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933135 | GGTAGGTTACGTCAT[A/G]CTGTTCTACCACAGG | 11060 |
rs774959911 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887384 | ATAAACTTGGCCTTG[A/C]TGCATTTAGCCCCAA | 11060 |
rs774979017 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819496 | ACTGGCCTTAAATCT[C/T]TCCTGAAACTGACCC | 11060 |
rs774981813 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826744 | AAAAAAAAAAAATTA[G/T]CCTAACACGGTGAAA | 11060 |
rs774994542 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861022 | CTGGCGCACCTGTAC[A/G]GGTTGTGCTCTGCAT | 11060 |
rs775002597 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911075 | CAGAAGTCCTGCCTC[C/T]AGGGAAGTATTAACC | 11060 |
rs775017644 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934328 | CGTGGACTGGCTCAC[C/T]CTCTCGGGGCTCCAC | 11060 |
rs775026569 | snp | A/C | 1.71173e-05 | 0.00292547 | intron-variant | WWP2 | GRCh38.p7 | 16:69929405 | AAGGACACCGGCTCT[A/C]CGTGTTTGAATCTGA | 11060 |
rs775046435 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897336 | TTGAACTCCTGGGCT[C/T]AAGCAATCTGCTCCC | 11060 |
rs775056359 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931142 | CCCTGAACATCTTTG[C/T]TCTTCCTAGGACGAA | 11060 |
rs775056850 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766034 | GCCTAGGCCTGTCTC[C/G]AGACTTCTAGATCTA | 11060 |
rs775062910 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69934899 | TCCATGGGCGCTGCC[A/G]TTCACGCCACGCTGC | 11060 |
rs775079816 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797247 | TGAAGGCTATGAGCG[A/G]AAGAAGAAATGTAGA | 11060 |
rs775096272 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856359 | CAATGGGAATGTTCT[A/G]TGTCTCAGTTGTGGT | 11060 |
rs775105467 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69825976 | TCAAACATAAATAAA[A/C]GTAGAAGCAGCCAGG | 11060 |
rs775146260 | snp | A/G | 6.59761e-05 | 0.00574314 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69930244 | TAAGGATCCTCGCCC[A/G]GGGTTTGAGTCGGGG | 11060 |
rs775147051 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772266 | TAGGAAGGGGCAACT[G/T]CTTGGTTGAACTGGG | 11060 |
rs775180834 | in-del | -/TT/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795649 | CTTAAAAATAGGAGG[-/TT/TTT]TTTTTTTTTTTTTTT | 11060 |
rs775187046 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813539 | GCTGGAGTGCAGTAG[C/T]GCAATCTCAGCTTCC | 11060 |
rs775208468 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | WWP2 | GRCh38.p7 | 16:69934035 | TATTTGAATATGCCG[A/G]AAAGAACAATTACTG | 11060 |
rs775228063 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905353 | CCTCCTAGTGGTGCA[A/C]AATGTGTACCTTCTT | 11060 |
rs775231290 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796247 | AGGAAAAAGTGTGTA[C/T]GTGTATGAGCGCAGA | 11060 |
rs775233863 | in-del | -/TAAAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803917 | CGTCTCAAAAAAAAA[-/TAAAG]TAAAGGAATAAAGAA | 11060 |
rs775294892 | snp | A/G | 1.6543e-05 | 0.00287597 | missense | WWP2 | GRCh38.p7 | 16:69937597 | GCGACTGGCAGAAGA[A/G]CACCATCTACCGGCA | 11060 |
rs775316719 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905794 | ATTTCAGTTCATCTT[C/T]CTTTTCTGCCCATTC | 11060 |
rs775326898 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | WWP2 | GRCh38.p7 | 16:69934135 | CATCGCCATGGTAAG[A/G]GGGCCCCAGGGGTCT | 11060 |
rs775337887 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803362 | TTTACTTTGGAACAT[G/T]TACATAAAAAAAACA | 11060 |
rs775354631 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818879 | CTCCTTGCTTTAAAT[G/T]TGGCCTATATGCCCA | 11060 |
rs775364475 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812125 | GTATTTATGTCTTTC[A/G]TGACATTGGCATCGG | 11060 |
rs775385150 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916901 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 11060 |
rs775389700 | snp | A/G | 6.60175e-05 | 0.00574494 | intron-variant | WWP2 | GRCh38.p7 | 16:69939320 | TCTGCTGACGTCGGC[A/G]TGTTTTACCTTGGAT | 11060 |
rs775403071 | snp | C/G | 1.64773e-05 | 0.00287026 | missense | WWP2 | GRCh38.p7 | 16:69936328 | GAGAACAACCTGGAA[C/G]AATGTGGCCTGGAGC | 11060 |
rs775416843 | snp | A/C | 1.7741e-05 | 0.00297829 | intron-variant | WWP2 | GRCh38.p7 | 16:69937697 | ACATTTGGGCCATCA[A/C]CCAAAGGAAACGGGT | 11060 |
rs775421511 | snp | C/T | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909475 | GTGCCCTGTTTGGTT[C/T]AGCTGTCAGGCGTGT | 11060 |
rs775423722 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793083 | ATTCACTGCTGGGCG[A/C]GGTGGCTCATGCCTG | 11060 |
rs775427221 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773387 | TTTCACTATGTTGGC[C/T]GGGCTGATCTCGAAC | 11060 |
rs775427622 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876840 | GTAATATGTTGAAAG[A/G]AATCTTTTTTCCTGA | 11060 |
rs775440876 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761178 | GGCACAGTGGCATTC[A/G]CCTGTAGTCTCAGCT | 11060 |
rs775450275 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821406 | TGTTCCAACAATCCT[G/T]CACCCTGTGTCACTG | 11060 |
rs775490653 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69761335 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCGGA | 11060 |
rs775504517 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862619 | TGGGCCTGAATCTGG[G/T]GTCAATGAACCTCCC | 11060 |
rs775520513 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900313 | ATACTGCCAACCTTT[C/T]ATCTGCAAAAATGTT | 11060 |
rs775545830 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792057 | GAGAAATAACCATTT[A/G]AATAGCGTAGGTGGT | 11060 |
rs775548102 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809200 | AATGTGGATTGCAAC[A/T]GGGCAGTGGGCTTTT | 11060 |
rs775587817 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69841214 | GGGGAAGTTAGATAT[C/T]AAATGAGTAAACACA | 11060 |
rs775587838 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817168 | CATTATACATATTTC[C/T]TTGTAACTTGATTTT | 11060 |
rs775611228 | snp | A/T | 1.69654e-05 | 0.00291246 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931461 | AGACAGGAGAACAGA[A/T]GACCACTTGAGGCTC | 11060 |
rs775628084 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781402 | CCAGGCTGGAGTGCG[A/G]TGGCACAATCTTGGC | 11060 |
rs775668093 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855148 | CGCTGAGCCCCAGCC[A/G]GCTTTTCATTTTGTT | 11060 |
rs775668691 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919943 | GGACTACAGGCATGC[A/G]CAGTCACACCTGGCT | 11060 |
rs775701030 | snp | C/T | 8.36155e-05 | 0.00646535 | intron-variant | WWP2 | GRCh38.p7 | 16:69936015 | CCCCTTGCCCCACCG[C/T]GCTGATAGGAGGGAC | 11060 |
rs775706283 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779778 | ATAATGGATTTCCAG[C/T]GTTTAGTGCTTTAAC | 11060 |
rs775736915 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834367 | CGTGACTTCCCCCAT[C/T]CTTTAGTCTTTGCTC | 11060 |
rs775754649 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931950 | CAGGCTACAGCATCA[A/G]TGGCCAGAAAGCTGC | 11060 |
rs775771784 | snp | G/T | 1.69158e-05 | 0.00290819 | intron-variant | WWP2 | GRCh38.p7 | 16:69871778 | CAGTGACTTATGTCT[G/T]TCTGCTTTCTACTTT | 11060 |
rs775772100 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853677 | CTGGTGAGGTTACAA[C/T]TGATGACTAGCCTTG | 11060 |
rs775784524 | snp | C/T | 3.22295e-05 | 0.00401419 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939101 | CTGCCGCCTGCCCGT[C/T]GGGGGATTTGCCGAA | 11060 |
rs775819093 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923381 | AAATTTTTTAAAAAC[C/G]CTTTAACGAAAGAGA | 11060 |
rs775835928 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809952 | CCTTGCTCTTGGTGT[A/G]GAACAATGTTTGCAG | 11060 |
rs775844473 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791382 | CAGGCACCTGCCACC[-/A]ACACCCGGCTAATTT | 11060 |
rs775861184 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69859234 | AACATTCTTATCTGC[A/C]TACACTGGGGAAGAA | 11060 |
rs775871149 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69914293 | ACCACACGCCTAGCC[C/T]AGAGGATAAAAAAAG | 11060 |
rs775895211 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845910 | AAAAATTAGCCAGGC[-/CA]ATGGTGGTGTGTGCC | 11060 |
rs775898714 | snp | C/T | 1.70481e-05 | 0.00291955 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888239 | CAGGCCCCCGACGCT[C/T]TGCCTGCTGGGTGAG | 11060 |
rs775925383 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789078 | ATTATTATATTTTGC[A/G]ACAGAGTCTCGCTCT | 11060 |
rs775978126 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894711 | CTGCTTTGGTCTGCA[A/G]GCCCTGTATCTGTTT | 11060 |
rs775990884 | snp | A/G | 9.8837e-05 | 0.00702914 | missense | WWP2 | GRCh38.p7 | 16:69908786 | CGAGAGCTGCCCAAC[A/G]GACGTGTCTATTATG | 11060 |
rs776002743 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816154 | ACCACTATTTCAATC[-/T]TGTGGAATGATTACA | 11060 |
rs776015555 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69789672 | TGCCTTCCTTGGAAG[A/G]AATACCCTTCTAGCA | 11060 |
rs776016578 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846051 | CAGACTCCATCTCAA[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 11060 |
rs776017242 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868103 | TTATTTTAAAGGTAA[C/T]ACAAGAGCCAAAAAC | 11060 |
rs776026921 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828996 | ACATGTGCAAGTCAC[A/C]TCCTCAGACTTGGTC | 11060 |
rs776053002 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911356 | GTGATCACTGTGAAA[C/G]AAGAGGATTGAGGAG | 11060 |
rs776066032 | snp | C/T | 1.71557e-05 | 0.00292875 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931926 | AGGCTGCCCTGTACC[C/T]CGCTTCCCCAGGCTA | 11060 |
rs776068182 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893909 | GATACTGTGCAGCAC[A/G]GCTCCTCTTCACTGA | 11060 |
rs776074454 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69763907 | GAGAAGCTTGTGATT[A/G]TCTGTGTCATTGGTC | 11060 |
rs776077841 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888309 | CTGAGGCTCCTTTAC[A/G]GGGGTGGAAACAACG | 11060 |
rs776125108 | snp | A/G | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940571 | TGTCTAAGCTGCCTG[A/G]GTATCCACGGGACAA | 11060 |
rs776145892 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870382 | CTTGGCTCCCTGAAA[A/C]CTCTACCTTCTGGGC | 11060 |
rs776151376 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | WWP2 | GRCh38.p7 | 16:69840156 | TGACCCTGAACCTGC[A/G]GACGGAGAACAAAGG | 11060 |
rs776154431 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848900 | GTGATTTTTTTACAT[C/G]GAAAAGTTTCAGAGC | 11060 |
rs776155666 | snp | C/T | 1.65214e-05 | 0.0028741 | missense | WWP2 | GRCh38.p7 | 16:69937170 | GAGCAGACCAAAGCC[C/T]TCCTGGATGGCTTCA | 11060 |
rs776164971 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69912145 | ATACAAAAAATTAGC[C/T]AGGCATGGTGGCACA | 11060 |
rs776192637 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873919 | AGCTATATTTCCCCT[A/T]CATTTATTTTTAGGT | 11060 |
rs776194189 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | WWP2 | GRCh38.p7 | 16:69934104 | ACCTCACCTACTTTC[A/G]CTTTATAGGCAGATT | 11060 |
rs776218589 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885830 | AGATAATCTAAAGTG[A/C]TTTGCACCTTTCCTG | 11060 |
rs776251528 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69836525 | AGCCAGAGGTCTCAA[A/G]TAGAACAGAGGAGGG | 11060 |
rs776258935 | snp | A/G | 1.70478e-05 | 0.00291952 | intron-variant | WWP2 | GRCh38.p7 | 16:69799339 | GATTCTTGGGTGGGG[A/G]TGGGAGGACCTGGCA | 11060 |
rs776281930 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69934019 | AACCCTATGTATTGT[C/T]TATTTGAATATGCCG | 11060 |
rs776284799 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783827 | AGAGTTGTGGTGGCA[C/T]ATCTATAGTCCCAGC | 11060 |
rs776289468 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69818681 | CTGCTTGACATATGT[G/T]CTGCCTTGGTTTCAG | 11060 |
rs776290018 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69764606 | ATGAAGTTTAGAAAA[C/T]GCTGTACTCTACCAT | 11060 |
rs776304990 | in-del | -/ACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795276 | CACACACACACACAC[-/ACA]CACACACACACACAC | 11060 |
rs776308428 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794173 | TCTACCTCCCTTAGC[C/T]TCCCAAAGTGCTGGG | 11060 |
rs776373700 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69871557 | GTAGGGGCAATTCAC[C/T]CTGGATTTGTTTACT | 11060 |
rs776380127 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69806437 | TTTTATAAAGTAAAT[G/T]GATGTGCTTTCCAAC | 11060 |
rs776384837 | snp | A/G | 3.29571e-05 | 0.00405924 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69925449 | CGAGTGCTTCGACTG[A/G]CCATGATCCCCTGGG | 11060 |
rs776392173 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896359 | CTTGGAGGCTCAAGC[A/G]ATCCTCCTATCTTGG | 11060 |
rs776420750 | in-del | -/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69941546 | CAGGGTGCAAGCTGC[-/T]TGGTGAGGTTTGGAA | 11060 |
rs776450176 | snp | C/T | 8.27096e-05 | 0.00643024 | missense | WWP2 | GRCh38.p7 | 16:69937579 | TGCAGGAGATAGACA[C/T]GAGCGACTGGCAGAA | 11060 |
rs776457458 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931526 | AAATGCCCTACCTAG[C/T]CACGTGAAGATCAGC | 11060 |
rs776475086 | snp | A/G | 6.76716e-05 | 0.00581646 | missense | WWP2 | GRCh38.p7 | 16:69871884 | CTCGGAGCCGGCACC[A/G]CCAGCCCGTCAAGAA | 11060 |
rs776531565 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906830 | GGCTGTAGTGAGCTA[C/T]GATCACACCACCACA | 11060 |
rs776553368 | snp | G/T | 1.65089e-05 | 0.00287301 | intron-variant | WWP2 | GRCh38.p7 | 16:69925532 | CTTCCGTCAGCCACG[G/T]TGCTCTGTCCTCTCC | 11060 |
rs776558787 | snp | A/G | 2.31463e-05 | 0.00340185 | intron-variant | WWP2 | GRCh38.p7 | 16:69871951 | GTGATGGCACCGCAC[A/G]CCAGCCTGCACTGAA | 11060 |
rs776602638 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813419 | CACCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 11060 |
rs776612270 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938214 | AGACAGGGTCTTGCT[A/C]TGGTGCCCAGCCTGG | 11060 |
rs776615058 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855050 | TTTGTAGAGATAAGG[C/T]CTCCCCAGGCTGGTC | 11060 |
rs776625004 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69843371 | TCCATGGCAACTGAA[C/T]GTCTAGGCAGGAAAA | 11060 |
rs776643222 | snp | A/T | 3.33311e-05 | 0.00408221 | intron-variant | WWP2 | GRCh38.p7 | 16:69787132 | GCCCAGGGAAGAGGG[A/T]GAATCTAACCACACC | 11060 |
rs776666922 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891434 | ATGCCTTTATCTTTT[A/G]TGAGGATATATAAAT | 11060 |
rs776737596 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798593 | TTATTTTTTAAAGCA[A/G]TAACTAAAAAGAGCC | 11060 |
rs776752933 | snp | A/T | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760811 | TCAGTCAAGAATGTC[A/T]ATTTAAAATGTTCTT | 11060 |
rs776810014 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69819755 | TTTAAAATGATTTTT[A/G]AAAATCATTAATTCA | 11060 |
rs776816621 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908935 | ACGGTCCCTTTCTGC[A/G]GAGGTAGCATAGCAC | 11060 |
rs776819186 | snp | A/G | 1.66338e-05 | 0.00288386 | missense | WWP2 | GRCh38.p7 | 16:69935877 | CATGGAAAGTTCATC[A/G]ACACGGGCTTCACCC | 11060 |
rs776834403 | snp | A/G | 3.30732e-05 | 0.00406638 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931830 | AACCCTATGACCTGC[A/G]CCGCCGGCTCTACAT | 11060 |
rs776845940 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886628 | AGCTGGGTGTGGTGG[C/T]GCACACCTGTAATCC | 11060 |
rs776855545 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900466 | AGACTCTGTCTCTAT[A/T]TTTAAAAAAGATAAT | 11060 |
rs776856653 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790972 | TATTACATTATTGAT[C/T]GTTTTTGTAGTCTTG | 11060 |
rs776858542 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802306 | GGTGTATAGGTTAGT[A/G]GTGTTAAGTACATTC | 11060 |
rs776891804 | in-del | -/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69836781 | GCCAGACCTGGGTGA[-/T]TTTTTTGTATTTTTA | 11060 |
rs776897893 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69937326 | TGTACCCACAGACAC[C/T]CAGCGTAAAACTCCC | 11060 |
rs776898394 | in-del | -/ACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816769 | TATACATATACACAT[-/ACAC]ACATACACATATACA | 11060 |
rs776905280 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69921641 | TTGCTTCACCGTTGC[A/G]GTTTCTTTTTGCCGT | 11060 |
rs776912111 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69862363 | AGCTACCGCGCCTGG[C/G]CCTTGTTTTGTTTTT | 11060 |
rs776915745 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | WWP2 | GRCh38.p7 | 16:69917783 | CCACCACCTGGCAGC[A/G]TCCGACCGCGGAGTA | 11060 |
rs776953004 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779571 | AAAAGTTTGGTCTTT[C/G/T]TTCTGTTGAACAGGC | 11060 |
rs776996491 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809107 | GTAGCTATTGCTGCT[A/G]TTGCTGGCACCAGCC | 11060 |
rs777023336 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | WWP2 | GRCh38.p7 | 16:69888171 | CCCCAGCCACACCGG[C/G]TGAAGGAGAGGAACC | 11060 |
rs777024997 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904839 | ATGCCCGGGAGAGAA[A/G]ACATCCCTACATGCT | 11060 |
rs777050923 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767658 | GATGGAGGGAAGTTT[C/T]ACAGGGTTGTGCTGG | 11060 |
rs777053571 | snp | C/T | 1.68329e-05 | 0.00290106 | intron-variant | WWP2 | GRCh38.p7 | 16:69929581 | TGGGTCTCTGTGCAG[C/T]TCCAGCACTGGGCAG | 11060 |
rs777054191 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69787341 | ACGCCTGTAATTCAG[C/T]ACTTTGGGAGGCTGA | 11060 |
rs777080600 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854217 | GTGTTGGAGAAATGA[C/T]TTTCTAGTCTTGAGA | 11060 |
rs777086626 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809766 | AGAGTGAAACTCCGT[C/G]AGAAAGAGAAAGAGA | 11060 |
rs777097298 | snp | C/T | 8.36561e-05 | 0.00646692 | missense | WWP2 | GRCh38.p7 | 16:69871841 | TCAGCCAGAACAACC[C/T]CAGCAACCGGCGAGC | 11060 |
rs777116579 | snp | G/T | 3.33267e-05 | 0.00408194 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931772 | GTGGAAGGGAGAGTG[G/T]CAGGCTGGCCCGATG | 11060 |
rs777121448 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69929367 | ACTCAGACCCAGCAC[C/G]CAGGAGGTGGGAACC | 11060 |
rs777141840 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905552 | TTTCAGATTAGGGAT[A/G]TTCAGCTGGTATGTA | 11060 |
rs777143460 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | WWP2 | GRCh38.p7 | 16:69930215 | GTGGACCACAATACC[C/T]GCACCACCACCTTTA | 11060 |
rs777185043 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922739 | TCCTTCTGGCTTTAT[A/T]TTTCAAGTTGTACTG | 11060 |
rs777191918 | in-del | -/TTGACT | 0.00047796 | 0.0154516 | intron-variant | WWP2 | GRCh38.p7 | 16:69908744 | TGTCTCATGCTACCC[-/TTGACT]TTATTTTTCAGATGG | 11060 |
rs777195882 | snp | C/T | 5.0218e-05 | 0.00501064 | intron-variant | WWP2 | GRCh38.p7 | 16:69936481 | GCCGGGGGCTCCGCT[C/T]CAGGGGTGGCGTGGA | 11060 |
rs777204935 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845795 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 11060 |
rs777211564 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | WWP2 | GRCh38.p7 | 16:69930188 | TACACCAGCGAGGGG[A/G]TGCGATACTTTGTGG | 11060 |
rs777212788 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894849 | GCTCCCTCGGTCCCA[C/T]ACACACAGAGGCACA | 11060 |
rs777216670 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826864 | GAATGGTGTGAACCC[A/G]GTAGGCGGAGCTTGC | 11060 |
rs777235757 | snp | A/G | 3.37564e-05 | 0.00410817 | intron-variant | WWP2 | GRCh38.p7 | 16:69937662 | TGGCAGGTGGGTCCC[A/G]GGCCCAGGCCTTGGC | 11060 |
rs777237527 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915385 | CATCTTTGGTAGTGG[A/G]AAGTCCATAAGCGAT | 11060 |
rs777241143 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870075 | TTAAACTGCCTGTAC[A/G]TGAATCTTTGCATCA | 11060 |
rs777247341 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798173 | TCTTGGAAAGGAATG[A/G]GCAGTTTTAAGAACT | 11060 |
rs777256178 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812773 | TCAGTGCAGCATATC[A/T]GGGAGCTCATGACTC | 11060 |
rs777260414 | in-del | -/ATGTATCT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878680 | TTTATACATGGTTTC[-/ATGTATCT]ATGTATCTATGTGCT | 11060 |
rs777271626 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932493 | CGAGAGCTCAGTACA[A/G]TGGCTCTGTTATCTA | 11060 |
rs777275755 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849927 | CATAGATATTTATTT[-/G]GCATTTACTCTGTAT | 11060 |
rs777321759 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890981 | AACATGTACGATGGT[C/T]CAGAGAAGGGTGTCG | 11060 |
rs777329417 | snp | C/T | 1.65485e-05 | 0.00287645 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937559 | CCAGCTGATGCTGTG[C/T]GGCATGCAGGAGATA | 11060 |
rs777341260 | in-del | -/AA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795556 | CATAGAACAGAAAGC[-/AA]ATGTGGCAAAATGAT | 11060 |
rs777346130 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799911 | GGCATGGCCCATGGC[A/G]GTGGTATTGGACCCT | 11060 |
rs777382271 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932346 | AAAAACAAAACAAAC[-/AAAA]AAACAAAATACGTGA | 11060 |
rs777385607 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828127 | CTTGCCTATAGAGCA[C/T]TGGGACCCTGAATCA | 11060 |
rs777417962 | in-del | -/GGC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826962 | AAAAAAAGGGGGGGG[-/GGC]GGCGGAGAGAATAAT | 11060 |
rs777430516 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868917 | TTGAGACAGAGTCTC[C/T]CTCTGTGTTGTCCAG | 11060 |
rs777443262 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69842733 | GGAGTGCTATGGCAC[C/T]ATCACAGCTCATAGC | 11060 |
rs777453904 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876420 | CCTAGGCTGGAATGC[C/T]GTGGCATGATCTTGG | 11060 |
rs777473810 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769876 | AAGTGATCAGTGTCT[-/T]TTTTTTTTTTTTTTT | 11060 |
rs777476848 | snp | A/G | 1.64784e-05 | 0.00287035 | splice-donor-variant, synonymous-codon | WWP2 | GRCh38.p7 | 16:69908851 | GCCCCTTCCTCCAGG[A/G]TAGGTCATCAACTGA | 11060 |
rs777487418 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936745 | ATCTGCATCTTTCTC[C/T]GGGCCGAAAGGATCT | 11060 |
rs777497120 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920460 | TTTGAGCTGGGCCCA[A/G]AAGATTTTGCCTGCC | 11060 |
rs777510267 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69790392 | TTATTCAGTGGAAGT[G/T]GGTCATCATAAAGGT | 11060 |
rs777512308 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909161 | ATTCGGCAGGGCTTC[A/G]TGAGAATGCCGCCAA | 11060 |
rs777543919 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875614 | TTGTTGTCATTTCAA[C/T]AGTGTTCACAGCATT | 11060 |
rs777572335 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69849591 | AGCAGTTGGTAAATA[C/T]GGAATAGGATTGAGA | 11060 |
rs777572650 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861745 | CTTCTCTGGGTGGTG[A/G]ACACTGTTTCTTTTC | 11060 |
rs777600272 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899834 | TGTTTAATAATCTTA[C/T]AATCGATGGCATTTT | 11060 |
rs777602489 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931594 | AGGTTAGATCATGGT[A/G]CCCGAAACCAGTGGC | 11060 |
rs777622808 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831027 | TACTCTCACCCGCTT[A/T]TGATGGGCCTATGGG | 11060 |
rs777632700 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805982 | CAGAAGGATCACTTG[A/T]GGCCAGTAGTTTGAG | 11060 |
rs777633522 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884679 | TTAAAACATATTTGA[A/G]TCCAGTGCCTCATAA | 11060 |
rs777668170 | snp | A/G | 0.000461201 | 0.0151785 | missense | WWP2 | GRCh38.p7 | 16:69908769 | TTTTCAGATGGGAAC[A/G]GCGAGAGCTGCCCAA | 11060 |
rs777692533 | snp | A/C | 0.0024956 | 0.0352359 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931513 | TTTTTTTTCAGTCAA[A/C]TGCCCTACCTAGCCA | 11060 |
rs777693878 | snp | C/G | 1.64857e-05 | 0.00287099 | intron-variant | WWP2 | GRCh38.p7 | 16:69936302 | CCCACTTGGTCTCCT[C/G]TGCCCCCAGAGAGAA | 11060 |
rs777729788 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796034 | TCTTTTTTTTTTTGC[A/G]ATGATGGGCATCGAT | 11060 |
rs777756000 | snp | A/G | 1.64746e-05 | 0.00287002 | utr-variant-5-prime, missense | WWP2 | GRCh38.p7 | 16:69840129 | TGTACCCCACAGTGG[A/G]GAACATGCAGCTGAC | 11060 |
rs777770288 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69765655 | ATGGTGAAACCCCAT[C/G]TCTACCCAAAATACA | 11060 |
rs777789409 | snp | C/T | 3.31011e-05 | 0.0040681 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69937148 | GCGTTTCACCCGAGG[C/T]GTGGAAGAGCAGACC | 11060 |
rs777791475 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903388 | AAGTGTAATAAAATC[A/C]GTGTTTCTCTCCTTG | 11060 |
rs777798420 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894470 | ACTGAAGGCTGCTGA[A/G]ACCTGGGCTGAAGAT | 11060 |
rs777812254 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879698 | GCTGTACAAGTATCT[C/G]AGCCCAAGATTTCAG | 11060 |
rs777813599 | snp | A/G | 1.69458e-05 | 0.00291078 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931912 | TTGAGTGCCCCGGAA[A/G]GCTGCCCTGTACCCC | 11060 |
rs777815423 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796637 | GTCCTAAGTAATGCA[C/T]CATTTGTAGTCCCTA | 11060 |
rs777817772 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784894 | TCAAGGAAAACAACA[C/T]AGTATTTGTTACCAA | 11060 |
rs777848036 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69840226 | CGGGCCAACTGTTGA[C/T]CTGGGAAATGTGCCT | 11060 |
rs777867890 | snp | C/G | 1.66244e-05 | 0.00288304 | intron-variant | WWP2 | GRCh38.p7 | 16:69929547 | AAGGACTTGGGCTGA[C/G]AGGGGGGCCGGGCTG | 11060 |
rs777887542 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69904469 | CAACTCCTGGGCTCA[A/G]GTGATCCTCCTGCCT | 11060 |
rs777896554 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888888 | TTTTTGTATTTTTAG[C/T]AGAGATATGGTTTCG | 11060 |
rs777913742 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880641 | TTTTCTTTATATGAG[C/T]TTCACTCATCCCATG | 11060 |
rs777919781 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827043 | ACTTGTCCTTCATCT[G/T]TAGCTCCCATCTTTT | 11060 |
rs777930975 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844704 | ATCACACGTGGTAGA[C/T]ATTCAGTGCTAGTTA | 11060 |
rs777955761 | in-del | -/T | 1.6473e-05 | 0.00286988 | frameshift-variant | WWP2 | GRCh38.p7 | 16:69934028 | TATTGTTTATTTGAA[-/T]ATGCCGGAAAGAACA | 11060 |
rs777963501 | snp | A/T | 5.01567e-05 | 0.00500758 | missense | WWP2 | GRCh38.p7 | 16:69799177 | TTTGTTTTTCAGGAA[A/T]GTCACGGCACAGAGT | 11060 |
rs777972372 | in-del | -/ACA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795274 | TACACACACACACAC[-/ACA]CACACACACACACAC | 11060 |
rs777975409 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896045 | AGATTCTACTGTTGT[C/T]GGAGGCTGGGCCATG | 11060 |
rs777983182 | in-del | -/GA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877732 | TGTAGGGTATAAGGA[-/GA]GAGAGAGAGAGAGAA | 11060 |
rs777993465 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772124 | GCACCACTACACCTG[A/G]CTAATTTTGTATTTT | 11060 |
rs778074314 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69889156 | TGCCTACACACACAC[-/A]ACACACACACACACA | 11060 |
rs778104261 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813761 | CAGCTGTGAGCCACT[C/G]TGCCTGGCCTCTGGT | 11060 |
rs778144870 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856386 | TGGTGATGGTAACAC[A/C]ACTATAAACATTTGG | 11060 |
rs778152274 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906364 | GGTGTCAGCCACCGC[A/G]CCCGGCCTTACGTAT | 11060 |
rs778153185 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926759 | GACCAAAGAAAGATC[A/G]TTAGTATCTCAGAGA | 11060 |
rs778168809 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | WWP2 | GRCh38.p7 | 16:69934098 | CGGACCACCTCACCT[A/G]CTTTCGCTTTATAGG | 11060 |
rs778169010 | snp | C/T | 1.6896e-05 | 0.0029065 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939907 | GAAGCTGCTGTATGC[C/T]ATTGAGGAGACCGAG | 11060 |
rs778176737 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793641 | TCACGAGTCAAGTCA[C/T]GGGCCCAGGCAAAGT | 11060 |
rs778181468 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939455 | TCGGGGGGCCTCAGA[C/G]CCGATGAGCTCCTGG | 11060 |
rs778187696 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69888070 | AACAGCCACTGATCC[C/T]GAAGAACCTTCCGTT | 11060 |
rs778189712 | snp | G/T | 1.65002e-05 | 0.00287225 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931110 | AAATTGTTCATTTTC[G/T]GAGAAATCGCATGAA | 11060 |
rs778221314 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821160 | TCTGAAAAGCCCTCT[C/G]TGTGTCGCTTTCTAT | 11060 |
rs778221479 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69834076 | TTCTCCTGTAGCCAG[A/G]CTGGTTGTGCTACAG | 11060 |
rs778223916 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864202 | GTAAAACCCCTTCTC[C/T]ACCAAAAATGCAAAA | 11060 |
rs778231935 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850301 | CTGAGGCAGGAGAAT[A/G]GTGTGAACCCAGGAG | 11060 |
rs778247836 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799572 | CTGTCTGCCTCTGCT[C/T]CTCTTCCCGTTGCAG | 11060 |
rs778254383 | snp | A/G | 1.70749e-05 | 0.00292184 | intron-variant | WWP2 | GRCh38.p7 | 16:69917674 | GGATGGGAGTGGGGT[A/G]GTCATTATATTCATT | 11060 |
rs778264942 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69781450 | TCCTGGGCTCAAGGG[A/T]TCCTCCCAACTCTGT | 11060 |
rs778274418 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906498 | GTAGATACATCAGGC[C/T]TAATAGTAGAAGTTA | 11060 |
rs778276485 | snp | C/T | 9.22169e-05 | 0.00678969 | intron-variant | WWP2 | GRCh38.p7 | 16:69939016 | CTGTGCCTTGACTTG[C/T]GGACTTCCAGGTGGT | 11060 |
rs778277166 | snp | C/T | 3.29674e-05 | 0.00405988 | synonymous-codon, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931562 | CAGGCAGACGCTTTT[C/T]GAAGATTCCTTCCAA | 11060 |
rs778293263 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809575 | AGTTCGAGACCAGCC[G/T]GACCAACATGGTGGA | 11060 |
rs778309067 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69821854 | TGAGCCACCATGCCC[A/G]GCTATTTTTCTTTGT | 11060 |
rs778337264 | snp | A/G | 3.30382e-05 | 0.00406423 | missense | WWP2 | GRCh38.p7 | 16:69917831 | AGTGGCAGTCGCAGC[A/G]GAATCAGCTCCAGGG | 11060 |
rs778352535 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902484 | TCCAACCAAATGTTA[C/T]TCATTGAAGGCCAAG | 11060 |
rs778364190 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906294 | AGCCAGGATGATCTT[A/G]ATCTCCTGACCTTGT | 11060 |
rs778375727 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780438 | ACTGCTATGATGAAC[A/C]TCCTTGAACATGGCC | 11060 |
rs778382093 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69930126 | TTTCTTCCCGTGTTT[C/G]CAGGATGATCCAGGA | 11060 |
rs778384507 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873385 | ACTGTGAGTGCAGTG[A/G]CCTGACCTCCTCCCT | 11060 |
rs778427480 | snp | C/T | 0.000125805 | 0.0079301 | intron-variant | WWP2 | GRCh38.p7 | 16:69917927 | GGGGCCGCCTCCCTG[C/T]GCTTGCGAATGTGCA | 11060 |
rs778439731 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932059 | AACCCGCCAGGCGCG[A/G]TGGCTCACGCCTATA | 11060 |
rs778442560 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924810 | AGGAAAACATTCCTG[A/G]GGGAGGTGAGGGCTT | 11060 |
rs778552888 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901209 | TTGGAGGAAGAATAG[A/G]ACTTGGCTCAGAAAC | 11060 |
rs778577592 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877467 | CCCTATCGCTTTCTC[A/C]CTATCACTTTTCTTG | 11060 |
rs778582196 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69810911 | AGGTTCACACCACCA[C/T]GCCCAGCTAATTTTT | 11060 |
rs778594792 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853434 | GCCAGTCACCACCAC[C/G]ACAGGACAAATGGCT | 11060 |
rs778621819 | snp | C/T | 1.65135e-05 | 0.00287341 | missense | WWP2 | GRCh38.p7 | 16:69787021 | ATGATATGGCATCTG[C/T]CAGCTCTAGCCGGGC | 11060 |
rs778630224 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808693 | AGGCGTGAGCCACTG[C/T]GCCCGGCCATGGCCT | 11060 |
rs778661747 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902606 | GATGACCCATGTGAC[C/G]AAGATGCAGTGTTGA | 11060 |
rs778669294 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69886892 | GGGATACAACAAAAA[G/T]AATTTCTGCATTAGG | 11060 |
rs778697993 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848742 | TTTGTTTAAGAATGC[A/C]TGTGAACGCACATGA | 11060 |
rs778701541 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926525 | GAGCTGGATCTTCTC[A/G]ATGCAGACACTTCTG | 11060 |
rs778712560 | snp | A/C/G | 0.000101234 | 0.00711392 | | | GRCh38.p7 | 16:69799319 | GATGAAGGGGGTGCC[A/C/G]ACGTGATTCTTGGGT | 11060 |
rs778713844 | snp | C/G | | | | | GRCh38.p7 | 16:69859799 | TTTCTCTCCTGCCAC[C/G]TGCTGGAGAAGGCGC | 11060 |
rs778736168 | snp | C/T | 1.64923e-05 | 0.00287156 | | | GRCh38.p7 | 16:69936291 | GTAGACATCTCCCCA[C/T]TTGGTCTCCTGTGCC | 11060 |
rs778745117 | snp | A/T | | | | | GRCh38.p7 | 16:69764226 | TTATTTTGAGACAGG[A/T]TCTTACTCTGTTGCC | 11060 |
rs778782456 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817294 | CATGCTGTCACCCAA[A/G]CTGGAGTGCAGTGGT | 11060 |
rs778804032 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860455 | GGGAACAATTAGGAT[A/G]TTATGAGAGAATGAA | 11060 |
rs778834704 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922336 | TGTATTTGCTAGACA[G/T]TCTTTATTTCTGAGT | 11060 |
rs778860974 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69830194 | TCCAGCGCTCAGGCG[A/G]TCTCTCTGCCTTGGC | 11060 |
rs778871271 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805561 | CACCTTTCTGACTGG[C/G]AATCTTTTTGATTTA | 11060 |
rs778905446 | snp | A/C/G | 1.66283e-05 | 0.00288338 | missense | WWP2 | GRCh38.p7 | 16:69888221 | CAGCTCCCAGCGGCT[A/C/G]CCCAGGCCCCCGACG | 11060 |
rs778905479 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936931 | GATTTCAAAGACTCC[A/G]GTGTCTGCAGGTCAC | 11060 |
rs778906546 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69932285 | CAGTGAGCCGAGATC[A/G]TGCCATTGCACTCCA | 11060 |
rs778917940 | snp | A/C/T | 0.00016169 | 0.00899015 | intron-variant | WWP2 | GRCh38.p7 | 16:69939137 | CGGTATGTTTTCTCT[A/C/T]GCCCTCTGGCGTCCT | 11060 |
rs778922883 | snp | C/T | 1.68963e-05 | 0.00290652 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939884 | AAGAGCTACGAACAG[C/T]TGAGAGAGAAGCTGC | 11060 |
rs778928521 | snp | C/T | 1.65004e-05 | 0.00287227 | intron-variant | WWP2 | GRCh38.p7 | 16:69925523 | GCCCTTGGCCTTCCG[C/T]CAGCCACGGTGCTCT | 11060 |
rs778940839 | snp | C/T | 5.01467e-05 | 0.00500708 | intron-variant | WWP2 | GRCh38.p7 | 16:69936477 | AGGCGCCGGGGGCTC[C/T]GCTCCAGGGGTGGCG | 11060 |
rs779004802 | snp | A/C | 3.29636e-05 | 0.00405964 | missense | WWP2 | GRCh38.p7 | 16:69888049 | TTCAGTGAATGATGA[A/C]CCCACAACAGCCACT | 11060 |
rs779018661 | snp | C/T | 3.34007e-05 | 0.00408647 | intron-variant | WWP2 | GRCh38.p7 | 16:69929445 | TTTCTTCTCATGTGG[C/T]AGAGAAGAGACAGGA | 11060 |
rs779023119 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69915242 | GTTACAAGTAAGGAA[A/G]TGTACTTATAGTATT | 11060 |
rs779049291 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795977 | CTAAATGCCAGTATG[A/G]TCCTAGATTGGGGCC | 11060 |
rs779062345 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870569 | GCCTCCCAAAGTGTT[A/G]GGATAACAGGCGTGA | 11060 |
rs779096737 | snp | A/C/T | 3.30908e-05 | 0.00406749 | missense | WWP2 | GRCh38.p7 | 16:69798826 | GGAATGAGATCATCA[A/C/T]TTTGTAAGAGAAAGC | 11060 |
rs779101373 | snp | C/T | 2.22591e-05 | 0.00333602 | intron-variant | WWP2 | GRCh38.p7 | 16:69871946 | GGTGAGTGATGGCAC[C/T]GCACGCCAGCCTGCA | 11060 |
rs779113307 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69772036 | GTGTGATCTTAGCTC[A/G]CCATGACCTGTCTCC | 11060 |
rs779139917 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800290 | CTCCCTGATTGCTTT[A/G]TCTTCTGAATTGGTG | 11060 |
rs779156269 | in-del | -/AGAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69884010 | AAAAAATAAAAGCTT[-/AGAC]AGTATAAAGAATGTC | 11060 |
rs779169669 | in-del | -/T | 2.38957e-05 | 0.00345648 | intron-variant | WWP2 | GRCh38.p7 | 16:69842012 | TTTTCTTGTGATTGA[-/T]TTCCTTTCTAGGATC | 11060 |
rs779206433 | snp | C/T | 2.48333e-05 | 0.00352364 | intron-variant | WWP2 | GRCh38.p7 | 16:69939801 | CTATCAGAGCCCTGG[C/T]CTCCTAGGGCTGACT | 11060 |
rs779214018 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69905275 | CACTCTGGTCCTCAA[C/T]CAAGAGTTGTCCGCT | 11060 |
rs779219923 | snp | A/G | 0.000116151 | 0.00761984 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933226 | GCCACAAACAGCCCA[A/G]CAGCTGGGGACTGGC | 11060 |
rs779247718 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69879918 | AAAAATAATTAGGCC[C/T]GTGCATTTAAAAAAT | 11060 |
rs779263415 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820580 | AAAAATAGGACCACA[C/T]GTATTGTATATTGTG | 11060 |
rs779304564 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913981 | CGAGGCTGAGGAAGG[A/T]GAATCGCTTGAACCT | 11060 |
rs779324052 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898319 | AGGTGTGAGCCACCA[C/T]TCCCAGCCAGTTATT | 11060 |
rs779359862 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69856870 | TTTTGTTTTGTGTCC[A/G]CTTGGCATATTTTTT | 11060 |
rs779372839 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69805162 | CTCGTGCCTCAGACT[A/C]CTGAGTAGCTGGGAT | 11060 |
rs779374332 | snp | A/G | 1.70139e-05 | 0.00291662 | intron-variant | WWP2 | GRCh38.p7 | 16:69799150 | ATCTGCTTGGATGTA[A/G]TGAATCAGGTATTTG | 11060 |
rs779378287 | in-del | -/AGG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900418 | AGATTGCTTGAGCCC[-/AGG]AGGAGTTCAAAACCA | 11060 |
rs779392372 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926829 | ACCCTGCGTCGTCAG[C/T]AGGCAGGGGAAAATG | 11060 |
rs779393177 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69935850 | GTGCCTCTTCCTTCC[A/C]AGGCGCTGTACCATG | 11060 |
rs779401805 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778293 | TCCATTAGTTTCTTC[A/C]ATAATGAAATACTTT | 11060 |
rs779405823 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907454 | GCTTCCCAGAAAAGG[G/T]CAACTTCTCCTAGAC | 11060 |
rs779420807 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792502 | GATAAACTTGCTCAT[A/G]TCTTTATTTTAGCCT | 11060 |
rs779422086 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69899250 | CTTGGTGGTTCTTGC[C/T]TGTAACTTTAGCACT | 11060 |
rs779483511 | snp | C/T | 3.29968e-05 | 0.00406169 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69917748 | AGGCAGGTTTTACTA[C/T]GTGGATCACAATACT | 11060 |
rs779489112 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69891489 | TAGTGCCCAAGTTCT[A/G]TATTCGAGGTTTTAC | 11060 |
rs779500520 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69885700 | ACCAGGGTGTGAATT[A/G]GGTGCTATATGACCT | 11060 |
rs779516462 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791743 | CAGGCTGGTTTCAAA[C/T]TCCTGGACTCAAGCA | 11060 |
rs779529624 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779227 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACTGT | 11060 |
rs779538505 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69888591 | AAAACAGCTTTTCTC[-/T]CTTGAATTTTATCGT | 11060 |
rs779564891 | snp | A/G | | | upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69760372 | CTCACTCTGTCGCCC[A/G]GGCTGGAGTGCAGAG | 11060 |
rs779594319 | snp | C/T | 1.71531e-05 | 0.00292852 | missense | WWP2 | GRCh38.p7 | 16:69935854 | CTCTTCCTTCCCAGG[C/T]GCTGTACCATGGAAA | 11060 |
rs779619213 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69780379 | TTATCCATTCCCCCA[C/T]TGATGGGTATTTAAG | 11060 |
rs779619617 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766941 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCAGG | 11060 |
rs779620020 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875122 | GTTTGTTTCCAGACT[A/G]TCACAATAAAGTGAA | 11060 |
rs779643433 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69927658 | GCTTTGGCCCTTAAC[A/G]GGGCAGACGTGGAGG | 11060 |
rs779677207 | snp | C/G | 1.84684e-05 | 0.00303873 | missense | WWP2 | GRCh38.p7 | 16:69842057 | GAGACTCCAGTGGAA[C/G]AGCAGTAGCTCCAGA | 11060 |
rs779678418 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906683 | TGAGCCCAAGAGTTC[A/G]AGACCAGCCTGGGCA | 11060 |
rs779683937 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69769875 | CAAGTGATCAGTGTC[-/TT]TTTTTTTTTTTTTTT | 11060 |
rs779707234 | snp | A/G/T | 0.00112185 | 0.0236579 | missense, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69929496 | TGAACCATAACACTC[A/G/T]CACGACCCAGTGGGA | 11060 |
rs779714706 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69873659 | TCTGCGAGCATTTTT[C/G]TCTTAGAAAACTCAG | 11060 |
rs779723914 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69867550 | GCTTTGACCATCAAA[A/G]CTTAAATGCCAAGTG | 11060 |
rs779727204 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69850675 | GAAGGCAAGGAGGAG[C/T]AAGAGAACTTGATGT | 11060 |
rs779754440 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919140 | TGAGCCACCATCCCC[A/G]ACCACATTTAAATTT | 11060 |
rs779760708 | snp | A/G | | | missense | WWP2 | GRCh38.p7 | 16:69939103 | GCCGCCTGCCCGTCG[A/G]GGGATTTGCCGAACT | 11060 |
rs779775595 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69919014 | ACACCCGGCTAATTT[C/T]TGTATTTTTAGTAGA | 11060 |
rs779784766 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828607 | TGACCTCAGGTGATC[C/T]GCCTGCCTTGGCCTG | 11060 |
rs779794553 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893058 | ACAAATGCATCACCC[A/T]CTCTCCGGACTTAGG | 11060 |
rs779804271 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808624 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAGGT | 11060 |
rs779807765 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903082 | GGCAACTATTCTTCT[C/T]GCTAAGCCAGTTGAG | 11060 |
rs779827378 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840319 | GTGGGGCTGGGCGGG[A/G]GCCAGGAGGTGCTGA | 11060 |
rs779840757 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828668 | TCGTGCCTGGCCTAA[C/T]TTTTATATTTTTAGT | 11060 |
rs779844161 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69858789 | AAAAGAATGTTACTT[A/G]CCCTCTAAGAATAGG | 11060 |
rs779871851 | snp | C/T | 0.000139738 | 0.0083576 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939122 | ATTTGCCGAACTCAT[C/T]GGTATGTTTTCTCTC | 11060 |
rs779875642 | in-del | -/CC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812469 | GCGCCTGCCCCCAAC[-/CC]CCCCCCCCTTTTTTT | 11060 |
rs779904131 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69902661 | AGCCTTTTAATCTCA[A/G]TGTGAAGGAGTTGCT | 11060 |
rs779924440 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815403 | ACCTTGAACTCCTGG[A/C]CCTAGGCCATAGATC | 11060 |
rs779928691 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829409 | ACACAGCATGTCACA[A/G]GGCATTGCAATGTCC | 11060 |
rs779967288 | in-del | -/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826267 | AGTGAAACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 11060 |
rs779982171 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69939691 | AACACCCCATGGTCC[A/C]GGCACCTGCAATGTG | 11060 |
rs779994047 | snp | C/T | 1.69758e-05 | 0.00291335 | intron-variant | WWP2 | GRCh38.p7 | 16:69937098 | CTCAGACTCCACCCA[C/T]GGCTGCTCTTTGGTC | 11060 |
rs779996006 | snp | C/G | 6.61726e-05 | 0.00575169 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931804 | TCTGTCTTCCCAGAT[C/G]ATGAACATGAAACCC | 11060 |
rs780011796 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69824275 | AGGATTCTTGGAGTA[-/T]TTTTTCTTAGTGTAG | 11060 |
rs780014514 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817008 | CATAACCTCTATACA[C/T]TCTGCCTTCCAAGGA | 11060 |
rs780033890 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69938049 | GTATGGGTTTTGTTG[C/T]TGTCGTTATGAAATA | 11060 |
rs780046309 | snp | C/G | 1.64923e-05 | 0.00287156 | missense | WWP2 | GRCh38.p7 | 16:69930146 | ATGATCCAGGAACCA[C/G]CTCTGCCCCCAGGAT | 11060 |
rs780052601 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69922467 | CCAGGGACCATTACC[C/T]GGGAAGAGGATTCCA | 11060 |
rs780073698 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69762792 | AATGGGTTTATGGCG[C/T]GGAGCCAGAGGGAAA | 11060 |
rs780073902 | snp | A/G | | | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69909410 | CTTCCCCTGCCCTGA[A/G]TTTGTGGAGGGAAAG | 11060 |
rs780081211 | snp | A/G | 0.000117427 | 0.00766157 | intron-variant | WWP2 | GRCh38.p7 | 16:69939461 | GGCCTCAGACCCGAT[A/G]AGCTCCTGGGACAGC | 11060 |
rs780086179 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877642 | TTCCTTATCACTAAA[C/G]TTAATAATATCTAGT | 11060 |
rs780145999 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | WWP2 | GRCh38.p7 | 16:69925517 | TTCCTGGCCCTTGGC[C/T]TTCCGTCAGCCACGG | 11060 |
rs780149223 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69923976 | CAGTAATGATTCAAC[A/G]TGATTTGTGATGGAG | 11060 |
rs780163637 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69776279 | TCTTCTTCCCTGGAG[A/G]GTAGGCCATTGCTCT | 11060 |
rs780169440 | snp | A/G | 1.64923e-05 | 0.00287156 | missense | WWP2 | GRCh38.p7 | 16:69939370 | CAGAAGTTTTGCATT[A/G]ACAAAGTTGGCAAGG | 11060 |
rs780174348 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69906174 | GCCTTCCGGGTTCAC[A/G]CCATTCTCCTCCCTC | 11060 |
rs780177862 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69804182 | TGTTTTTAACTTTCT[A/G]TAGTCCAATCTGTCA | 11060 |
rs780185202 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887901 | AAAGTCATGTTTTGT[A/G]AAACTTTTTGCTGTC | 11060 |
rs780201957 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69823007 | CCAGGCATGGTGGCA[C/T]GTAATCTCAGCTACT | 11060 |
rs780236524 | snp | A/G | 0.000100694 | 0.00709484 | intron-variant | WWP2 | GRCh38.p7 | 16:69871936 | CAATGGCACAGGTGA[A/G]TGATGGCACCGCACG | 11060 |
rs780242601 | in-del | -/C | 5.06385e-05 | 0.00503157 | intron-variant | WWP2 | GRCh38.p7 | 16:69871797 | GCTTTCTACTTTGAA[-/C]CCCCAGGACGCACAG | 11060 |
rs780249921 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864642 | GCCACCTTGGCCTCT[C/T]GGGGTTCAAGCGATC | 11060 |
rs780261684 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69794027 | GGTTCAAGCGATTCT[C/T]GTGTCTTAGCCTCCT | 11060 |
rs780297339 | in-del | -/TT | 0.01119 | 0.0739581 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931494 | TTTAAAGTTCTTTTC[-/TT]TTTTTTTTTTCAGTC | 11060 |
rs780303806 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848573 | GCCCAGGAATTTGAG[A/G]CTATAGTGAGCCAAG | 11060 |
rs780309295 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870747 | AAAGTAGTAGATGCT[C/T]ACTAAGTAGTAGAAG | 11060 |
rs780353556 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882541 | AGAAGTTGAAACCAC[A/G]CATCAGCAAAGTCAA | 11060 |
rs780379591 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69913316 | GGGATTACAGGCGTG[A/G]GCCACCACGCCCAGC | 11060 |
rs780388643 | in-del | -/TCTG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828330 | CTCTAGCTGTTCTTC[-/TCTG]TCTTTCTTGCAAGGT | 11060 |
rs780399445 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69869904 | CCCAGCAGGGTCGTT[C/G]TGCTGGAGGTGGATC | 11060 |
rs780422338 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802408 | TTAAACCATGACTCC[C/T]CCATCCTCCCCTCGC | 11060 |
rs780426023 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69854437 | AGGTCTGTGGAGGTG[C/G]TGATTTGGGGTTTGG | 11060 |
rs780453140 | snp | C/G | 0.00173074 | 0.0293662 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933206 | ACGGACTCCTCGTCT[C/G]CCCAGCCACAAACAG | 11060 |
rs780463790 | snp | C/T | 1.671e-05 | 0.00289045 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931491 | CGATTTAAAGTTCTT[C/T]TCTTTTTTTTTTTTC | 11060 |
rs780481704 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP2 | GRCh38.p7 | 16:69837357 | AGGCATGAGCCACTG[C/T]ACCCAGCCCATTGGC | 11060 |
rs780510975 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | WWP2 | GRCh38.p7 | 16:69888031 | AAGTATGATTTGTGC[A/G]TCTTCAGTGAATGAT | 11060 |
rs780516281 | snp | A/G | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942023 | CTCCAAGCAGTTGCT[A/G]TGGGGTGCAGAACAA | 11060 |
rs780517590 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69855765 | GAACAGTGGAGAGGC[C/T]AGTCCCACTGGAGAG | 11060 |
rs780523046 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69811495 | TGGTGGCTTATACCT[C/T]CCCACACTTTGGGAG | 11060 |
rs780540753 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69783185 | CGGCTAATTCTTGTA[G/T]TTTTAGTAGAGATGG | 11060 |
rs780542642 | snp | A/G | 1.65798e-05 | 0.00287917 | intron-variant | WWP2 | GRCh38.p7 | 16:69937520 | GGGGAGGGACCTGCC[A/G]GGGATGCTGACTGCC | 11060 |
rs780544814 | snp | G/T | 1.67055e-05 | 0.00289006 | intron-variant, nc-transcript-variant | WWP2, MIR140 | GRCh38.p7 | 16:69933100 | TCTCTCTCTGTGTCC[G/T]GCCAGTGGTTTTACC | 11060 |
rs780578021 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69876355 | GCATGTTTTTTGGGG[G/T]TTTTTTTTTTTTTCG | 11060 |
rs780579077 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799967 | AGTACCATATGTGGC[A/G]AATGAATGGCATGGA | 11060 |
rs780584459 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831110 | TTATGTTAATGGCCA[A/G]ATCAGTCACATCTTC | 11060 |
rs780604830 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69860672 | GGAGCCTGCCTCCGT[C/T]CTGCTGAATTCCTGC | 11060 |
rs780634641 | snp | C/G | 3.33567e-05 | 0.00408378 | intron-variant | WWP2 | GRCh38.p7 | 16:69937274 | GGACCCTGAGCCCCT[C/G]CCTCTGGGGCGATCC | 11060 |
rs780638270 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69926942 | GTAGAGGCAGGTGAT[A/G]TAGCCCAGTCAAGTG | 11060 |
rs780639432 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69777596 | ATGAGCCACCGTGCT[C/T]GGCCTATATTTTCTT | 11060 |
rs780640267 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936667 | CCAGCTGTGCTTTTT[C/T]GCCATGTGGGAGACT | 11060 |
rs780645035 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784327 | CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCC | 11060 |
rs780658889 | snp | A/G | 1.76721e-05 | 0.00297249 | intron-variant | WWP2 | GRCh38.p7 | 16:69935816 | TGGCAGTGCCCAGGG[A/G]AGGCCAAACCTCTGT | 11060 |
rs780665132 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69801991 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACC | 11060 |
rs780694295 | snp | A/G/T | 4.9603e-05 | 0.00497991 | missense | WWP2 | GRCh38.p7 | 16:69798820 | TTCTCTGGAATGAGA[A/G/T]CATCATTTTGTAAGA | 11060 |
rs780721383 | snp | A/G | 0.000341933 | 0.0130709 | intron-variant | WWP2 | GRCh38.p7 | 16:69937675 | CCGGGCCCAGGCCTT[A/G]GCAGGGACATTTGGG | 11060 |
rs780728138 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69936077 | TTTATTTTGTCTGCC[A/G]GTGTGGCCCCTGAGC | 11060 |
rs780734762 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69771682 | TCAATTGCTGAAAAA[C/T]AATTCTCTTTTTCTC | 11060 |
rs780754657 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791517 | ACAGGCGTAAGCCAC[C/T]GCACCTGGCCTCTTT | 11060 |
rs780762440 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813675 | GTTTCACCATGTTGC[C/T]CAAGGCTGGTCTTAA | 11060 |
rs780825825 | snp | C/T | 9.85497e-05 | 0.00701891 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69939047 | GAAGGAGATGGACAA[C/T]GAGAAGAGGATCCGG | 11060 |
rs780825994 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898398 | AGATCTTCAACTTCA[A/G]TAGGTATTATCAAAT | 11060 |
rs780828684 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887415 | CACTTTTTTTTTTTG[A/T]GACACAATTTTGCTG | 11060 |
rs780854302 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69875345 | ACTGGTGGAAGGTCT[C/T]TCCTCGATGTTGATG | 11060 |
rs780872650 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69851866 | TGCGCTCCTGGAGTC[C/T]CAGCTACTCGGGAGG | 11060 |
rs780890962 | snp | C/G | 3.73065e-05 | 0.00431878 | missense | WWP2 | GRCh38.p7 | 16:69842048 | TGCCTTCGAGAGACT[C/G]CAGTGGAACAGCAGT | 11060 |
rs780901524 | snp | A/G | 3.29652e-05 | 0.00405974 | intron-variant, utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69908862 | CAGGGTAGGTCATCA[A/G]CTGAGAAGACCTGAG | 11060 |
rs780903172 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69768065 | CTGGTCTTGAACTCC[A/G]GGCTCAAGTGATCCT | 11060 |
rs780916047 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69779158 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 11060 |
rs780927392 | snp | C/G | 3.3384e-05 | 0.00408545 | intron-variant | WWP2 | GRCh38.p7 | 16:69936470 | GAGTCTCAGGCGCCG[C/G]GGGCTCCGCTCCAGG | 11060 |
rs780928999 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908236 | GGCAACAGAGTGAGA[C/T]CCTGTTTCATTAAAA | 11060 |
rs780929622 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796881 | AGAGGAAGATAGTTA[C/T]TGCTATAAAAAATCT | 11060 |
rs780957211 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69883770 | GAAGAGCTACTATGG[G/T]TGAACCAGGTTGACT | 11060 |
rs781017151 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69907568 | CATTATATAAATACA[C/T]TTTTGCATCCTTTAT | 11060 |
rs781023946 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69766882 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 11060 |
rs781049236 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69893274 | TGCCTCTCTGCTATT[C/G]TTGGCTCTGCACACC | 11060 |
rs781073651 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827528 | TAAAAAAACTCCAAT[C/G]TATACAAGGGAATTT | 11060 |
rs781112716 | snp | C/T | | | utr-variant-3-prime | WWP2 | GRCh38.p7 | 16:69940118 | GCCCTGCAGTTCCCC[C/T]GACCCGCGGATGGCA | 11060 |
rs781118278 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931602 | TCATGGTGCCCGAAA[C/T]CAGTGGCAGGCCGAC | 11060 |
rs781127329 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69808542 | GAATAGTTGACATTA[C/T]AGGCACCTGCCACCA | 11060 |
rs781136305 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890257 | TACTACGTACGTATT[-/G]TTTTCCTAGCATGCG | 11060 |
rs781150084 | in-del | -/ATC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69767419 | GTCCTTCTACCACTT[-/ATC]ATTAGTGAGATGGGT | 11060 |
rs781168121 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828428 | CTGGAGTACAACAGC[A/G]CGATCTCAGCTCACC | 11060 |
rs781202978 | snp | A/G | 6.64187e-05 | 0.00576237 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69799186 | CAGGAATGTCACGGC[A/G]CAGAGTCATTTAGAT | 11060 |
rs781206542 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69897829 | AGAAGAATGGTTTGA[A/T]CCAGGGAGGCGGAGG | 11060 |
rs781213004 | snp | A/C/T | 3.29708e-05 | 0.00406011 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69936408 | GCTGAAGGAGGGCGG[A/C/T]GAGAGCATCCGGGTC | 11060 |
rs781219605 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69773265 | CTCACTGCAACCTTC[A/G]CCTCCCAGGTTCAAG | 11060 |
rs781220292 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69816796 | ATATACACACACACA[C/T]ATATACACACATGCA | 11060 |
rs781220607 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887983 | AAAAACCTAGCAAGT[A/G]TAAATAAAATTCTCA | 11060 |
rs781220739 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69797784 | ATCCCAGCTACTCAG[A/G]AGGCTAAGGCAGGAG | 11060 |
rs781221157 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845362 | CAAGGACTGTAGTTG[C/G]GAGGTGATGAATCAG | 11060 |
rs781240187 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69868466 | GGAGTTGATCATGGA[C/G]ATGTCTGTCTGAGGG | 11060 |
rs781247205 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69846669 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 11060 |
rs781284452 | snp | C/T | 1.65078e-05 | 0.00287291 | missense | WWP2 | GRCh38.p7 | 16:69888201 | CCAGCACTTCGGGTA[C/T]ACAGCAGCTCCCAGC | 11060 |
rs781293765 | snp | A/G | 1.66582e-05 | 0.00288597 | splice-donor-variant | WWP2 | GRCh38.p7 | 16:69799296 | ACAATGGGGGCAAAA[A/G]TACGTATGATGAAGG | 11060 |
rs781304874 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803811 | TACTCAGGAGTCTGA[C/G]GCCGGGGAGTCACTT | 11060 |
rs781305796 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788096 | GGCCAGGTGTGGTGA[C/T]TCATGCCTGTAATAT | 11060 |
rs781308964 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896980 | TTTTAAAATCCATTC[A/G]TTTTTATTGTAAAAT | 11060 |
rs781313683 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69911664 | AAGAGTGCAATCGTG[C/T]TTCTTAGAAGTGGAA | 11060 |
rs781320277 | snp | A/G | 5.67832e-05 | 0.00532808 | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933195 | CCTCTGCGTCGACGG[A/G]CTCCTCGTCTGCCCA | 11060 |
rs781363218 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69844918 | AAATATTATCCAAAG[A/G]CTGTCTCTTTGCCTC | 11060 |
rs781423690 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69878765 | TTCATCTAACCATTC[C/G]TTAATTCTTGTGTAT | 11060 |
rs781424308 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69803119 | TTTTTTTCCTATTTG[A/G]TAACTATTAACATTA | 11060 |
rs781493234 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69925685 | TAACCAAGCTCCACC[A/G]AACCACTGTAGCATC | 11060 |
rs781495985 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69861911 | TTAAGAGTGTGCTCA[A/G]AGGAAGGACAGACTT | 11060 |
rs781501910 | snp | C/T | 3.40942e-05 | 0.00412867 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931917 | TGCCCCGGAAGGCTG[C/T]CCTGTACCCCGCTTC | 11060 |
rs781506986 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69870953 | TTCTGCATTGCTTCT[C/T]ATTTACTTGGATGGA | 11060 |
rs781514045 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887119 | AGTGATCATCAAAGA[A/G]GTGAAGAGATGGTGA | 11060 |
rs781525422 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69895619 | AAATACAAACAAAAA[C/T]ATCAGCTGTGTGCAC | 11060 |
rs781536706 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898893 | GTATTTAGTAGAGAC[-/G]GGAATTCACCATGTT | 11060 |
rs781546150 | snp | C/T | | | downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69942104 | TTCCAGGCAGTCATT[C/T]ATTTGGGAAATACTC | 11060 |
rs781557823 | in-del | -/AG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69827376 | TCCAGCCTGGGCGAC[-/AG]AGACTCCATCTCAAA | 11060 |
rs781583005 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924085 | TCTGTGTGGGCAGGA[C/G]GCCCTGCCCTGAAAG | 11060 |
rs781587412 | snp | A/G | 1.65712e-05 | 0.00287843 | splice-donor-variant | WWP2 | GRCh38.p7 | 16:69937239 | GAGAAAGAGCTGGAG[A/G]TGAGTGTCTGAGGTT | 11060 |
rs781603811 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792832 | GAGTAACTGGAACTA[C/G]AGGTGTGAGCCACTA | 11060 |
rs781606052 | snp | C/G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69896468 | AAAGAATATTGTGTC[C/G/T]GTCTTTGTGTTCCCT | 11060 |
rs781613655 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69784946 | TTTTTTTAAAGAAAA[A/G]AAAGAGTGGTCGAGT | 11060 |
rs781621999 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931213 | AAGTATCACCAGTTC[C/T]GTTTCCTCTGCCATG | 11060 |
rs781627179 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69848173 | CAGCTGGGCGCAGTG[A/G]CTCAGCGTGCAGGCT | 11060 |
rs781627825 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69835668 | TTTGAAGGTAAATTG[C/G]AGATATCATGACACT | 11060 |
rs781647766 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69864473 | AGTGGCTGTGTTCCC[A/G]CCATCAATGTATGAG | 11060 |
rs781667264 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69828430 | GGAGTACAACAGCGC[-/G]ATCTCAGCTCACCAC | 11060 |
rs781679346 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69793722 | CAATAGCGATGTTAT[C/T]TATGGGAGCAATTGG | 11060 |
rs781688077 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant, upstream-variant-2KB | WWP2, MIR140 | GRCh38.p7 | 16:69931126 | GAGAAATCGCATGAA[C/T]CCCTGAACATCTTTG | 11060 |
rs781688135 | snp | C/G | 1.65031e-05 | 0.00287251 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69935915 | CTACAAGCGGATGCT[C/G]AATAAGAGACCAACC | 11060 |
rs781701646 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69798242 | AAGGCATGCAGATGT[A/T]TATGTTCACGGTAAT | 11060 |
rs781724320 | snp | A/T | | | intron-variant, downstream-variant-500B | WWP2, MIR140 | GRCh38.p7 | 16:69933450 | TTCTCATCTGAAGGC[A/T]GCATGGATTACATTG | 11060 |
rs781724437 | snp | C/T | 8.37023e-05 | 0.00646871 | synonymous-codon | WWP2 | GRCh38.p7 | 16:69871852 | AACCCCAGCAACCGG[C/T]GAGCAAAGCCCCGGT | 11060 |
rs781763876 | snp | A/G | 1.82467e-05 | 0.00302043 | missense | WWP2 | GRCh38.p7 | 16:69871919 | GGCCACAGTGGCTTG[A/G]CCAATGGCACAGGTG | 11060 |
rs781769373 | snp | C/T | | | intron-variant, utr-variant-5-prime | WWP2 | GRCh38.p7 | 16:69783116 | CCCAGGTTCAAGCGA[C/T]TCTTCTGCCTCAGCC | 11060 |
rs796075283 | in-del | -/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69785224 | TTAGGTGTGTGAGAC[-/TG]TCTCAAAAAAAAAAA | 11060 |
rs796090205 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887402 | ATTTAGCCCCAACAC[-/T]TTTTTTTTTTTGAGA | 11060 |
rs796098246 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69916051 | CAAAAAAAAAAAAAA[-/A]TCTTTGGTAACAAAA | 11060 |
rs796115867 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69809116 | GCTGCTGTTGCTGGC[A/C]CCAGCCGTAGCACGT | 11060 |
rs796123274 | in-del | -/GAAAG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69903782 | AAAAAAAAAAAAAAA[-/GAAAG]AAAGAAAAATGTGTT | 11060 |
rs796133455 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69882956 | TCAGGAGTTCCAGAC[A/C]AGCCTGGCCAACATA | 11060 |
rs796137970 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69900536 | CAACTTTTTTTTTTT[-/T]CTTTGAGACAGAGTC | 11060 |
rs796145390 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69924221 | TGTCCTTTCAGCTGG[G/T]GGTGGAGGGAGGGCT | 11060 |
rs796165160 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69880282 | CTGTGATTTTTTTTT[-/T]AGTGTTGATCACTTT | 11060 |
rs796199052 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69796020 | ATTTTTTTTTCTTTC[-/T]TTTTTTTTTTTGCGA | 11060 |
rs796275747 | in-del | -/TTT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69894243 | ACTATACCCAGGCTA[-/TTT]TTTTTTTTTTTTTTG | 11060 |
rs796293286 | multinucleotide-polymorphism | CT/GG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826958 | AAAAAAAAAAAGGGG[CT/GG]GGGGCGGAGAGAATA | 11060 |
rs796307145 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815787 | CAAGACTCCGTCTCG[-/A]AAAAAAAAAAAAAAA | 11060 |
rs796404333 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69799050 | GAGGGGAAAGGATAT[-/A]ATGTGGGTGTCTGCC | 11060 |
rs796410241 | in-del | -/GA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69877730 | AATGTAGGGTATAAG[-/GA]GAGAGAGAGAGAGAG | 11060 |
rs796447402 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69802618 | TGTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCGC | 11060 |
rs796448456 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69931007 | TCTTTTTTATTCTTC[A/G]AGGATCTTAATGACA | 11060 |
rs796475371 | in-del | CACACAC/TAT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795261 | AAAAAATGCGGATAC[CACACAC/TAT]CACACACACACACAC | 11060 |
rs796519846 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69813723 | ATCCTCCCACGTTGG[C/T]GTCCCAAAGTGCTGT | 11060 |
rs796523418 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69845338 | GAGGCATTACCGGTG[C/T]GTTTACATCAAGGAC | 11060 |
rs796533023 | in-del | -/CT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69831827 | GGAAAAAAACAAAAC[-/CT]TTTTTTTTTTTTTTT | 11060 |
rs796537462 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69908709 | TCCTTTCTAACAGGG[-/G]CCTATGCCTTTCCAC | 11060 |
rs796548913 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69920821 | AATGCATTAAAGCAA[-/T]TTTTTTTTTCCCTTA | 11060 |
rs796574121 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69840433 | GATCAGTATCACAAC[A/G]TGAATTTTCAAGGGT | 11060 |
rs796604606 | in-del | -/ACAC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69820854 | CACACACACACACAC[-/ACAC]GACGTTGAAAGAGTG | 11060 |
rs796606703 | in-del | ACA/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69795274 | ACACACACACACACA[ACA/C]ACACACACACACACA | 11060 |
rs796617315 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69778474 | CGGAGTCATCTGTTC[A/G]TGTTGCTGAGACAGA | 11060 |
rs796635055 | in-del | -/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69826955 | AAAAAAAAAAAAAAA[-/G]GGGGGGGGGCGGAGA | 11060 |
rs796655591 | snp | C/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69901371 | TGTCTAAGTAACCAG[C/G]AAGACATCTTTTCTT | 11060 |
rs796675658 | in-del | -/T | | | intron-variant, downstream-variant-500B | WWP2 | GRCh38.p7 | 16:69910415 | TCTGTGTACTGTGGC[-/T]TTTTTTTTTTTTAGA | 11060 |
rs796693827 | in-del | CC/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69812476 | CCCCCAACCCCCCCC[CC/T]TTTTTTTTTTTTTTA | 11060 |
rs796704518 | snp | G/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69887409 | CCCCAACACTTTTTT[G/T]TTTTGAGACACAATT | 11060 |
rs796705204 | in-del | -/TT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898028 | TCTTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTG | 11060 |
rs796709639 | in-del | -/CA | | | intron-variant | WWP2 | GRCh38.p7 | 16:69918161 | TTTCATTTCTGCCCC[-/CA]CTTCATTCAAGTCCA | 11060 |
rs796714977 | multinucleotide-polymorphism | CA/TG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69788281 | TGTGATTGTGCCACT[CA/TG]ACTCCAGCCCAGGCA | 11060 |
rs796717493 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69800185 | TGGTCTTTTCTTTTC[A/G]GCTGGGCACATAGAG | 11060 |
rs796748436 | snp | C/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69898027 | TTCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 11060 |
rs796760252 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69817622 | TGGCCCTTTCTATTG[-/T]TTTTTTACAATTACT | 11060 |
rs796763813 | in-del | -/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69832544 | TTTATTTTTAAAAAA[-/T]TTTTTAATGTTTTTT | 11060 |
rs796782161 | in-del | -/A | | | intron-variant | WWP2 | GRCh38.p7 | 16:69774982 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 11060 |
rs796869832 | snp | A/G | | | intron-variant | WWP2 | GRCh38.p7 | 16:69829250 | CTGTCTGCTCTGCCT[A/G]TTTCTGTCCTTCCTT | 11060 |
rs796877359 | snp | A/C | | | intron-variant | WWP2 | GRCh38.p7 | 16:69853813 | GGTACTCCCAGATTC[A/C]TCTACTGTGCTGTCA | 11060 |
rs796914955 | in-del | -/CT | | | intron-variant | WWP2 | GRCh38.p7 | 16:69792447 | CACATAAAGTCGTGA[-/CT]CTGTGTATAAAGATA | 11060 |
rs796931977 | snp | A/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69863341 | AGGTAGTCACTATCA[A/T]AATCAAGATACAGAA | 11060 |
rs796972461 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP2 | GRCh38.p7 | 16:69774056 | AGTGTTGTTTTTTTT[-/T]AATGCTCCCCAGATA | 11060 |
rs796979099 | in-del | -/TC | | | intron-variant | WWP2 | GRCh38.p7 | 16:69791234 | CTTTTTTTCTTTCTT[-/TC]TTTTTTTTTTTGAGA | 11060 |
rs796991895 | in-del | -/GG | | | intron-variant | WWP2 | GRCh38.p7 | 16:69815500 | AAAAAAAAAAAAAAA[-/GG]AGAGGGGCAGGGGCT | 11060 |
rs797016514 | in-del | GG/T | | | intron-variant | WWP2 | GRCh38.p7 | 16:69890541 | TGTATGTTATAATTT[GG/T]GGGGGAACAATGCAG | 11060 |