SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs141794609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448082 | CATGATTTTTCTTTT[A/G]TCATTGTTCTCTAAG | 11059 |
rs141874808 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86374764 | TCCCTGGCTGGAGTA[C/T]GGTGGCGCAAACATA | 11059 |
rs141890424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393954 | TCACCATGGGAAATC[A/G]GCAACCATTGAGAAG | 11059 |
rs141900499 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86438812 | CTCAAAAATACACAC[A/G]GTAACCATTATTATT | 11059 |
rs141938005 | in-del | -/AAAAACA | 0.193653 | 0.243567 | intron-variant | WWP1 | GRCh38.p7 | 8:86360049 | GTGAGACTCCCTCTC[-/AAAAACA]AAAAACAAAAAACAA | 11059 |
rs142021880 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343427 | TGCAGCTCCCCATCC[C/T]CCGCCCCCCCAGCGC | 11059 |
rs142055373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429189 | GAGGAATTGAAAGGG[C/T]AGATGGCTCTGTTGT | 11059 |
rs142104013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86394704 | TGTGACAGAATAATA[C/T]CTTTTTCCCTCTGAC | 11059 |
rs142118529 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452654 | CTCTTCAGTGGCTAC[A/G]GTACTTCGATGAAAA | 11059 |
rs142130784 | snp | A/T | 0.0108692 | 0.0729142 | intron-variant | WWP1 | GRCh38.p7 | 8:86440638 | TAGGAATATATTAAG[A/T]TCTTCCTTAATGTCA | 11059 |
rs142183386 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | WWP1 | GRCh38.p7 | 8:86390391 | TCACGCCACTGCACT[C/T]CAGCCTGGGCAAGAT | 11059 |
rs142208282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86391754 | TACAAAAGCTTGGTC[A/G]GTGTAAATGCAATTA | 11059 |
rs142212058 | snp | A/C | 0.000319534 | 0.0126359 | intron-variant | WWP1 | GRCh38.p7 | 8:86425216 | TATTTTTGTATTTTT[A/C]TTAAAGGTGGGAACA | 11059 |
rs142220936 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | WWP1 | GRCh38.p7 | 8:86428377 | CCGTGAGAGGAGTGG[-/A]AAAAAACAAAACAAA | 11059 |
rs142234418 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86348538 | GACATTTCTTAAATC[A/T]ACAGTTCACTCACAG | 11059 |
rs142254340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346179 | GAGTCTGAGGGATGA[A/G]TTGGGTAGAGAAGAG | 11059 |
rs142256388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86461563 | GTGAAGGGAGCGACA[C/T]TCTGTAGAGAGAGTT | 11059 |
rs142374149 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86412487 | TTAATGATTAATTGT[C/T]TCTGCCTTCAAGAAG | 11059 |
rs142391057 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364315 | ATTTTGAGAACAAGG[C/T]TTTCATATAGCTTAG | 11059 |
rs142420457 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411733 | AATTGGAATCTGAAG[C/T]TAGAAGTATATTAGA | 11059 |
rs142431787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86405023 | ATCATTCTATTGGCC[A/G]GTTTACAGAGGCTTC | 11059 |
rs142445664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363199 | TTTGTGAGATGGGGA[C/T]GAGGAAACAACAACA | 11059 |
rs142455074 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86458995 | ATAAGTCTATACCTT[C/G]GAGTCATTCTTTTTC | 11059 |
rs142460291 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86407393 | TTCAGCACTGTTGAC[A/C]TATTGGCCCAGGTAA | 11059 |
rs142479237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86406842 | GCTGTGTATATGCAA[A/G]CAGTCATTTCTCATG | 11059 |
rs142494215 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453968 | TTGGTTCTTTCATGT[A/G]ATCAAATGTGCATAT | 11059 |
rs142525105 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | WWP1 | GRCh38.p7 | 8:86408812 | CTACTTGGGAGGCTG[G/T]GGCAGGAGAATTGCT | 11059 |
rs142550620 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86356314 | TCTGTAAGTTTGGAA[C/G]CCAAGTTTTAATGTT | 11059 |
rs142558218 | snp | G/T | 0.00980159 | 0.0693161 | intron-variant | WWP1 | GRCh38.p7 | 8:86435564 | CTTATACTCAATAAT[G/T]TAGTCTTCTCTTTAT | 11059 |
rs142563904 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368377 | ATCCACTCAGACAAT[G/T]AAGTGGGAAATTTTA | 11059 |
rs142678266 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86376412 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 11059 |
rs142752321 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86381732 | TTTTGTATCCATAAA[G/T]AACTTCAGTTATTGC | 11059 |
rs142758930 | snp | C/T | 6.5937e-05 | 0.00574144 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442752 | CATCTTTCATACTTC[C/T]GTTTCATTGGTCGTT | 11059 |
rs142763873 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86387420 | AATCTTGATTTCTAA[G/T]CTTTTAAAATATATT | 11059 |
rs142905480 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86382709 | CATCTCAAACCCGCA[A/G]AAAACCAGGGTTCTA | 11059 |
rs142913912 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86428123 | TTTTACTAATTTTCA[A/G]TCTTCCACTTTTATA | 11059 |
rs142955198 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86447042 | AGGAATGAAATAGTC[A/G]TCTAGGAAAGTGGGA | 11059 |
rs142962904 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86394221 | GTTTTCAACAAATCC[A/G]TGATTTATAGAACAG | 11059 |
rs142990880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86451320 | CAAGAGCAGAATTGA[C/T]GTATTAAGGGGATAA | 11059 |
rs143003933 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86389364 | GTGATGACTCTTAAC[A/G]AGTATGCTGCCTTCA | 11059 |
rs143032000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86432670 | TGGAGTGCAATGATG[C/T]GATGTCAGCTCACTG | 11059 |
rs143055808 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375061 | ATAATATCTGTTTTT[-/A]ATCCTACTACACCAG | 11059 |
rs143082655 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | WWP1 | GRCh38.p7 | 8:86352440 | ATGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGGC | 11059 |
rs143113633 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467776 | GGTAATGTAAACTCT[A/G]CCACTTTTTTGTGTT | 11059 |
rs143134054 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86356449 | TATATTTATATATAT[A/T]TTTTTTTTTACTGTA | 11059 |
rs143208760 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86453633 | TTTTCTATATCAGTT[G/T]CATCATTTTACATTC | 11059 |
rs143246965 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86404178 | GATGCTAAACTGGCA[A/G]GTAAAATGCACATAT | 11059 |
rs143312824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382245 | AGTTTCCATGATACT[A/T]TTTCTAGACTGGGAT | 11059 |
rs143316407 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86352919 | AGCAGAAATTATTTT[C/G]AGTGAAGCTAATTCT | 11059 |
rs143348237 | in-del | -/TATTTATTTATTTATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422320 | AGAAGTACCAGTTTG[-/TATTTATTTATTTATT]TATTTATTTATTTAT | 11059 |
rs143350294 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86398031 | TTGTGCAGAAATTTT[A/G]CCTCAACCACAAGAG | 11059 |
rs143350413 | snp | C/G | 0.00230358 | 0.0338597 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427736 | TACCATGGAATCTGT[C/G]CGAAATTTTGAACAG | 11059 |
rs143374425 | snp | A/T | 0.000186759 | 0.0096615 | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468725 | ACAAGAGACAAAACC[A/T]GCTTTGTTTTGGAGA | 11059 |
rs143427826 | in-del | -/AG | 0.408359 | 0.193449 | intron-variant | WWP1 | GRCh38.p7 | 8:86392774 | TATCAACACAAACTC[-/AG]ATATTTTGAAGTCAA | 11059 |
rs143427846 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86426208 | ACTATGACAAGATCA[A/T]CAAGTTATAGTCATT | 11059 |
rs143452845 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86385504 | CATTTTTTTAAAAAA[A/T]GTTTATGGTGTGAAT | 11059 |
rs143496169 | snp | A/G | 3.29821e-05 | 0.00406078 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398458 | CAAGAAAATATAACA[A/G]ACTGCAGCTCATCTC | 11059 |
rs143558812 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86379212 | TATTAGTCCAGTGGC[A/G/T]CTGAACTTAGAGCAG | 11059 |
rs143615954 | in-del | -/ATCTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415398 | TATTGTGCTTGCCTT[-/ATCTC]ATCTCTTCATCTCTT | 11059 |
rs143616789 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86408144 | AGTTGGAGTCCTACA[G/T]TGTGGGTAGCCTTTT | 11059 |
rs143701426 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359693 | GGATCTTGTGTTAGT[A/G]ATCATCATCAGTGAA | 11059 |
rs143708541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383116 | ATAATAATTTTTATA[C/T]ATTTGGCTTAAAACT | 11059 |
rs143728798 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86399487 | TGGACTCATTACCTT[C/T]GAAAAAGCATGCTAG | 11059 |
rs143731208 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86373824 | GGCAACATTCTAATG[C/T]TTATTTTTATTTTTG | 11059 |
rs143870333 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385023 | AGTAAGACACTGTCT[-/C]AAAAAAAAAAAAAAG | 11059 |
rs143872016 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86404126 | CTGAAAGGAAATGCT[C/T]GTTGGAGCATTTCAG | 11059 |
rs143872208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354893 | GGGCACCTTCTTATT[C/G]CTGATTCTAGAAAGA | 11059 |
rs143926153 | in-del | -/AACTGTAAGCATAAATTA | 0.0399052 | 0.1355 | intron-variant | WWP1 | GRCh38.p7 | 8:86356899 | CAAGGTTGTTTCCAC[-/AACTGTAAGCATAAATTA]AATTGTTCTCTGATG | 11059 |
rs143927237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360500 | ACCTAGGTTCTGCCC[C/G]CTATGCAGTAGGCCT | 11059 |
rs143953971 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86396437 | GTGCTTTCGTATTTC[C/T]TTTAGTTTTTCTAGT | 11059 |
rs143975359 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WWP1 | GRCh38.p7 | 8:86449942 | TCAATAGAGATCATT[C/T]AGGTTGTGTCCAGTT | 11059 |
rs143975846 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86459141 | TTCAAGTGATTCTCC[C/T]GCCTCAGCACCCCCA | 11059 |
rs143984118 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WWP1 | GRCh38.p7 | 8:86375928 | GCCTAACCAAAATCT[A/G]TTGTCAAGCTTTGGG | 11059 |
rs143995711 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441943 | TCTAGTTGGATTTCG[C/T]ATATTGGACTTTAAA | 11059 |
rs144025894 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402552 | CCACCTCAGCCTCCC[C/T]AAAGTGTTGGGATTA | 11059 |
rs144058947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440412 | CTCTGTTGCTTTTAC[A/G]TATAAACAACAATTT | 11059 |
rs144060832 | snp | C/G | 0.000924428 | 0.0214793 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448460 | TTCACATGACCTGAA[C/G]TTGGGAGGTTCCAAT | 11059 |
rs144064477 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | WWP1 | GRCh38.p7 | 8:86400458 | GAATGGAAGGGAGCC[C/T]ATTTTTAAAAGAGAT | 11059 |
rs144069737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86417855 | TGAGAGCCTTGTTCT[A/G]GGCATGTGCAGCAGG | 11059 |
rs144084001 | snp | C/T | 0.000247196 | 0.0111147 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402129 | ACACACCTTCATCTC[C/T]GTCTCAGGTTGCTGC | 11059 |
rs144129917 | snp | A/G | 0.00013231 | 0.0081325 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448416 | GAAATGTACTTTTCT[A/G]TTGACATGGAGATTT | 11059 |
rs144227479 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86391483 | TATGTTTCACTCAGT[C/T]AGCCTCACTATTTCT | 11059 |
rs144246400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86434298 | GATCTGACCCCTCTT[A/G]TCTCTTCAACCTCCT | 11059 |
rs144271667 | in-del | -/T | 0.0383715 | 0.133092 | intron-variant | WWP1 | GRCh38.p7 | 8:86377088 | AGACCTCTGTATTGA[-/T]TTTTTTCTTTTTTTT | 11059 |
rs144302512 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341257 | GTTTAAAGCAGAGAT[G/T]AGTGGGCACATATGG | 11059 |
rs144318125 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86386254 | TTCTTTAACATAGGT[A/G]GAATTATTATGGAGA | 11059 |
rs144337448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419483 | AGATACAACATACAT[A/G]CAACAAGAACCCAAT | 11059 |
rs144369196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455033 | CTTACCATAGTAATG[G/T]TTATTTATACTATTA | 11059 |
rs144376260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86350615 | GCACGGATAGAGTTA[C/T]ATGAAGGTGCTTCTT | 11059 |
rs144382154 | snp | A/C/G | 9.90318e-05 | 0.00703613 | intron-variant | WWP1 | GRCh38.p7 | 8:86431531 | CGTCTTGCATATATC[A/C/G]GTAGGTAGAACCAAC | 11059 |
rs144523216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86355511 | AATATCAGTTTGAAT[A/G]AAGTGACCAATTACT | 11059 |
rs144541743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355792 | CACAAAACCACCTGA[C/T]GTAAGCTTTAGTTGA | 11059 |
rs144554205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434381 | CTGTGCCTTCAACAC[C/T]TTCAGCTTCCACCTT | 11059 |
rs144657283 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86350000 | TGTCCCCCACGCGCT[C/T]CAAGCCCCAATGGCA | 11059 |
rs144668491 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86429262 | CATGGCCTTCTGCCT[A/G]TACCTCATTGGCCAG | 11059 |
rs144734650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413728 | GCATTTGAGGCAGCA[A/C]GATATATAATGCTGA | 11059 |
rs144792972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373112 | CATGGTTTCTTTTGA[A/T]TCACTAAATATTTAG | 11059 |
rs144795103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86455152 | TGAAAACTCTTACCA[C/T]ACTAGGAATATAAGG | 11059 |
rs144854743 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86382331 | TGGGGGTATGTACAT[A/G]TATGTGTAATTCTGG | 11059 |
rs144868463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374488 | AAGTGGGATTACACA[C/G]TACTGTAATTCCCAT | 11059 |
rs144890490 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86351827 | TAACAGTCGTCTGGG[A/T]TGCTTATTAAACATG | 11059 |
rs144891512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432336 | ACCACCATATCTGTC[A/C]GTCTCCTACCATCTC | 11059 |
rs144926323 | in-del | -/TTTATTTA | 0.40853 | 0.193309 | intron-variant | WWP1 | GRCh38.p7 | 8:86352221 | AGCTAATTTTTTATT[-/TTTATTTA]TTTATTTATTTATTT | 11059 |
rs144931777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417026 | CCAAGCCTTGGACAC[A/G]TACCCTGGGAGTGAC | 11059 |
rs144931888 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WWP1 | GRCh38.p7 | 8:86370015 | AAGAACTAGATCAAT[C/T]CCAATATGGTTAAAG | 11059 |
rs144934971 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86376867 | TTGTCTTTGTCTTCC[A/G]TTTTGTTGATCTAAT | 11059 |
rs145000575 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86425132 | TTTAATGTAAAGCTT[A/G]TCTGTAATTTTTCTG | 11059 |
rs145012542 | snp | A/G | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461776 | TTTCTTGGTGTAGGA[A/G]GTAATGGGCCTCAAA | 11059 |
rs145053082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383799 | TAATTGAGTAGGATA[C/T]GGATATGCTCAGGAA | 11059 |
rs145089406 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433317 | CATGTGCCTGCTAAT[A/G]ACTCACAAATTTAGC | 11059 |
rs145134390 | in-del | -/G | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341134 | GTCCAGATCCCTGCT[-/G]GGGGAATACCTACGG | 11059 |
rs145155697 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86392990 | TGTAAATATTTGCCA[A/C]ATTATTAGATAAAAA | 11059 |
rs145176277 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86436751 | GTGGAGAATTTTTCA[C/T]AATGAGACGTCTTAT | 11059 |
rs145206055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391878 | GCATTTTAAAGGAAT[A/G]TCTTTCAGGCCCTTG | 11059 |
rs145224459 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86461421 | AAAGATTACTCTTCT[A/G]TGCTGTAGGTAGGGC | 11059 |
rs145279263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378813 | CTGTAATGAACTCAG[A/G]GAAGAGTTAATACTA | 11059 |
rs145295743 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86350384 | AGTGGAGTAGTGAAT[G/T]CATTTCATTTTAAGA | 11059 |
rs145302197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346591 | GGTTAAAGTGTAGTG[C/T]GATTGGTAAACAGTT | 11059 |
rs145349940 | in-del | -/T | 0.190205 | 0.242744 | intron-variant | WWP1 | GRCh38.p7 | 8:86463631 | ATGTGATTTTTTTTT[-/T]CTATTATATAATTAA | 11059 |
rs145371963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86445735 | TGAGAAATTTCCAAC[C/T]TGCTTTTCAAAGTGG | 11059 |
rs145405148 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86375507 | TACATGTGCAGTATA[C/T]GTATCTCATCTCTCC | 11059 |
rs145405822 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | WWP1 | GRCh38.p7 | 8:86349456 | TTGGGGCCACCCATG[-/T]TAACAGATTACCATA | 11059 |
rs145437325 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86458432 | AAGAATGATCGAGGG[G/T]ATAATGTCTAAGAAT | 11059 |
rs145460359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392826 | TTCACATTCAATGAT[G/T]TAAGTGCCTCTTTAT | 11059 |
rs145462274 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411599 | CACGGGTACTCCAGT[A/G]GTGTCTGAAGAAAAT | 11059 |
rs145462512 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86406469 | TATTATATTTTTTTC[A/T]TAGCTCTTTATTCTG | 11059 |
rs145475345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456701 | GAAAGTAACCTAAAT[A/G]TTCATTAACAAGTGA | 11059 |
rs145528161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411173 | TACACAAGGGAAGGG[C/T]GATTGAAAGGGATCA | 11059 |
rs145575404 | in-del | -/GC | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86463784 | TGCAAGACAGGCCAG[-/GC]GCACGGTGGCTCACA | 11059 |
rs145595682 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86420420 | TATGTTCCATGGCTC[A/T]TCTGTGGGGAGAGTT | 11059 |
rs145610172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461954 | TATTCATTAAAGTAG[C/T]CAGAATTTCAATTTT | 11059 |
rs145632516 | in-del | -/AAAG | 0.0383715 | 0.133092 | intron-variant | WWP1 | GRCh38.p7 | 8:86376586 | AAAAAAAAGAAAGAA[-/AAAG]AAAAGAAAAAGAAAA | 11059 |
rs145636948 | snp | C/T | 0.188631 | 0.242351 | intron-variant | WWP1 | GRCh38.p7 | 8:86372414 | ATCCACCCGCCTTGG[C/T]CTGCCAAAGTGCTGG | 11059 |
rs145660019 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341830 | GTAGATATAATCTAT[G/T]GGGGTTGGTCAGGTG | 11059 |
rs145673491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367373 | TGAATCAGATCTATT[A/C]TAATTGGATTTCTTT | 11059 |
rs145702038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415644 | CGAGATACAGAACAT[G/T]AATATCACCCTAGAA | 11059 |
rs145742545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86416352 | TTGTTTTGTAAAATG[A/G]AAGAGACTGACAGGT | 11059 |
rs145767678 | snp | A/G | 0.000562482 | 0.0167608 | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468751 | GGAGAATTCATCAGG[A/G]TCTTCCACTTTTCAT | 11059 |
rs145797818 | in-del | -/AG | 0.456095 | 0.141508 | intron-variant | WWP1 | GRCh38.p7 | 8:86405854 | CTTTCTAAATTCCAA[-/AG]AAAGTTATGAATTCT | 11059 |
rs145814822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373428 | AATCACCCACAACAA[C/T]GGCCAATTTGTCAAT | 11059 |
rs145818872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403575 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 11059 |
rs145851786 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86347713 | GTGAAATGTAGATAT[A/T]TATTTTTTTGAAAAT | 11059 |
rs145903511 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343550 | TTTCATCTTCGTGTT[C/G]TTTTTTTAAAAAAAT | 11059 |
rs145908332 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86421685 | AAAAATTAGCTGGGC[A/G]TGGTGGCTGGCGCCT | 11059 |
rs145918951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348565 | ACAGCACATACTGGC[A/G]TACCTACTATGTGCC | 11059 |
rs145919617 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86396959 | TCTCAAACTCCTAAG[C/T]TCAAGTGATCCTCCT | 11059 |
rs145955153 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440300 | TTTTTATTCCTAAAT[C/T]TTTTATTTAATTCAT | 11059 |
rs145979506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405509 | CAGGCATAGTGTAAT[A/G]TACAATATATATGCC | 11059 |
rs145987180 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86365975 | TTAACGTGGCACTGG[C/T]AAAATTGGAAACAAT | 11059 |
rs146099145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345319 | CCTGGAAAATTTCCA[C/T]ATGCGCCTATGCTTT | 11059 |
rs146123510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86428244 | GATTCTAAGAAGCAA[C/T]ACTCATCTGTTTTGC | 11059 |
rs146222252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366244 | GGCCATATGAGCTAG[C/T]GAATGGAATGGAGAT | 11059 |
rs146225070 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449389 | CAACTACTCACCTCT[A/C/G]TGGTATAGTGCAAAG | 11059 |
rs146247738 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86371187 | CAGGCATGAGCCACC[A/G]CCCCTACCTGTAGTT | 11059 |
rs146250530 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86453765 | CCCTAATGGGTGTGA[C/G]GGGATATCTCATTGT | 11059 |
rs146280768 | snp | C/T | 6.79648e-05 | 0.00582905 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448202 | TTACCATTCTACAAG[C/T]GTATGTTAAGTAAAA | 11059 |
rs146341676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86386739 | AGTTACAGGGATTCA[A/G]TTTTTTCCGTAGATA | 11059 |
rs146350155 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344770 | GAGGTATCTCTAAGA[C/G]AGCACAGAGTTCCTG | 11059 |
rs146369870 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341145 | CTGCTGGGGAATACC[A/T]ACGGAATTTCTGAGG | 11059 |
rs146370343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390538 | TCTCCACCAAAAAAT[A/G]CAAAAACCAGTCAGG | 11059 |
rs146421627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401676 | ATTAGGCTTAAATAT[A/T]TAAAATGTACAATTT | 11059 |
rs146425192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396643 | CTATTACTCCCACTC[A/G]AGTACAATAGTGCAA | 11059 |
rs146428704 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86450217 | AGCTTGGCATTCTTG[G/T]CCTCTTCTTATTTTT | 11059 |
rs146483796 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462376 | GAAGTAAACAAAGAC[A/C]CCGAAGAAATTGTTT | 11059 |
rs146502552 | snp | C/T | 3.31104e-05 | 0.00406867 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466904 | AATGAATGTGGCTTC[C/T]TATTTTGGAGGAGCT | 11059 |
rs146543566 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341651 | TCAAGGGAAAATTTA[A/G]GACCTAATCTTAAAA | 11059 |
rs146545999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419592 | AAGAAATTTGCCAGA[C/G]AGTAACACATAAGGA | 11059 |
rs146655800 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445812 | TGAAGCCTTGCCAAC[A/T]TCTGTTATTTTTTAA | 11059 |
rs146658223 | snp | A/G | 0.00294454 | 0.038257 | intron-variant | WWP1 | GRCh38.p7 | 8:86440702 | TTTTCTGTTCCATTT[A/G]TTCCATTTTTCTTCA | 11059 |
rs146663057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363135 | GGGGCAGTCTCCATT[C/G]TACAATATGGAATGA | 11059 |
rs146669466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436148 | TTGTATCTCCATGTT[A/G]TAGGTAAAGGTACTG | 11059 |
rs146784863 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86383432 | CGAAATGAAGCCCTC[A/T]CGAATTGTATAAGCT | 11059 |
rs146786253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86466074 | CTAGTCACTGCTACT[A/G]TAGGGACCAAAACCC | 11059 |
rs146788865 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86379314 | CACTCTTTAATTGCT[A/C/G]TGTTGCCGGTACTTA | 11059 |
rs146932216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421862 | ATATAAATTTACCAT[A/G]TTAACAAATAATCGG | 11059 |
rs146953102 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86389112 | ATAAACATTTATTGA[A/G]TTTTAGGAAGAGACA | 11059 |
rs146969291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385040 | AAAAAAAAAAAAAGT[A/T]AACAACTGCCAAGAA | 11059 |
rs146975792 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341904 | TCTCTGAAGTAGAAA[C/T]CGGGTCACCTGGTAA | 11059 |
rs147026965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453144 | TTGTGCATCCAATCT[C/T]CAGAAATTTTTCATC | 11059 |
rs147036968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447075 | GTGAATGCAGTAGGG[A/G]AATGTGATTACCAGG | 11059 |
rs147058787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406952 | GGGTGAGGACAAATA[C/T]GTGGTGCTTTGAGAT | 11059 |
rs147074886 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86404050 | TGGAGTGTCTCTAAT[A/C]TGAAAAATCTCAAAT | 11059 |
rs147126662 | snp | A/G | 0.000183457 | 0.00957575 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425223 | GTATTTTTATTAAAG[A/G]TGGGAACAAAGAAAA | 11059 |
rs147130289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86417576 | GCATTGTGCTTGGAA[C/T]GTAAGTGCTTACTGA | 11059 |
rs147146585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415228 | CCAGAGGTGTTTTTT[C/G]AGTCTCCTGTCCAAA | 11059 |
rs147190562 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86394538 | TCTTTTAGTGGTAAG[G/T]GCATTGAAGGAAATG | 11059 |
rs147233371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360829 | TAAAATAGGGCAAGG[C/T]GCTAGAGTTGGCCTA | 11059 |
rs147250288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355131 | AACTTAAAATTGGCA[C/T]TTTGGAATTGAAGAG | 11059 |
rs147297571 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86415775 | TAGGCTTCTTCTAAT[C/G]AGCATGATGTAACCT | 11059 |
rs147334542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417989 | GTCCGATAGTGACAA[A/G]TTCTATGAGACAAGA | 11059 |
rs147341548 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86382054 | CATGAAGAAGATAGA[C/T]AATTATAGAGTAATA | 11059 |
rs147357378 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | WWP1 | GRCh38.p7 | 8:86376425 | AATACAAAAATTAGC[C/T]GGGCATAGTGGCACA | 11059 |
rs147399265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434448 | TTTTCCCGAAACTCC[A/G]TATGGCTTTTGCCCT | 11059 |
rs147441715 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WWP1 | GRCh38.p7 | 8:86439500 | GCACTCAGTCTGAAT[A/C]TTTTCTTTTTTAAAA | 11059 |
rs147463115 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | WWP1 | GRCh38.p7 | 8:86394261 | TTATATACCTACCTC[C/T]TCAGAGACTCAAATT | 11059 |
rs147553353 | snp | C/G | 9.89234e-05 | 0.0070322 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461784 | TGTAGGAAGTAATGG[C/G]CCTCAAAAGTTTTGC | 11059 |
rs147612572 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86347564 | TCAGTTTTTTCCTTT[A/G]TGTTAAAATGGTAAT | 11059 |
rs147615845 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86391893 | GTCTTTCAGGCCCTT[A/G]AGAAAGACACTCACA | 11059 |
rs147648825 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86350385 | GTGGAGTAGTGAATG[C/T]ATTTCATTTTAAGAA | 11059 |
rs147685223 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407194 | TTAATTTTTTGCCCC[A/G]TGTTTCTGCATGAGC | 11059 |
rs147717608 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367399 | TCTTTCTTTCTTTCT[C/T]TTTCTTTCTTTCACA | 11059 |
rs147721113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86411350 | CCCTGAAATTTTGAG[C/G]AACAAAAATAAAATC | 11059 |
rs147753756 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86372642 | CAGTTTCATTTTTTT[C/T]CCATATGGATAATTC | 11059 |
rs147823010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388706 | TTTAGTTTTCACAAA[A/G]TCATTTCTTTTATAA | 11059 |
rs147891004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86451860 | CAGATTTTCTTCCTT[A/G]TTTCCTTTCTGTCAT | 11059 |
rs147893584 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368515 | TCAGATAAGCTCACT[A/G]TCTTAAATCTAACCC | 11059 |
rs147966518 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86410409 | TCAAACTCATTGATA[A/T]GAAATTGTACGTGGT | 11059 |
rs147977758 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86414656 | GATAGGACTATGGGT[A/G]CCTCAATCCTGTTGA | 11059 |
rs147990442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426491 | TGAATCCTGGAGGAT[A/G]AGTAGAATTCTGGTT | 11059 |
rs148052681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86447664 | ATTAATAGCTTCAGT[A/G]GATTTTTTTAGTTCC | 11059 |
rs148052948 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365599 | GTTATCAGGAGAGGG[A/G]CATTCTTGTGTTTTG | 11059 |
rs148106553 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86437840 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 11059 |
rs148150462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86393914 | ATATAGGCATTTCAG[A/G]TTTTGCCTTGTTCTC | 11059 |
rs148188975 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | WWP1 | GRCh38.p7 | 8:86376095 | TGATGAAGCTGATAG[C/G]TACTCCACTGAAGAA | 11059 |
rs148192844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344101 | CTTGTTTTTAGCCAT[C/T]AAGTAGTAAATTAGC | 11059 |
rs148243458 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86453678 | GAAAGATTCCAGTTT[C/G]TCCACATCTTTCCCA | 11059 |
rs148266302 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86404281 | CTTGAATATGGATTT[A/G]GAGGTTTTGATCTTA | 11059 |
rs148317590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398184 | AGCGTGGGATTGAGG[C/G]GGAAAGAGGAATTAC | 11059 |
rs148344407 | snp | A/T | 1.65326e-05 | 0.00287507 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430727 | GCAGAAAATGACCCT[A/T]ATGGACCTTTGCCAC | 11059 |
rs148422464 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86371406 | TTAGCTTTAAATGAT[A/G]ATGCCAAATTATTTT | 11059 |
rs148467388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355940 | TAGCTTTGAGCCCAA[A/G]GAAATCTGGCTTCAA | 11059 |
rs148496362 | snp | A/G | 3.3018e-05 | 0.00406299 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381538 | TACATTGGAATTTCA[A/G]GTTTGGAGCCATCGC | 11059 |
rs148518905 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86350310 | CTGCTAAGTAATGCC[A/G]TGGTTAAAGGTGAAA | 11059 |
rs148521067 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86429362 | CTCCAACAAAACAGG[A/G]TTTTGGTTCTCAAGA | 11059 |
rs148556107 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86382597 | CCAGCTACTTGGGAG[G/T]CTGAGGCAGGAGAAT | 11059 |
rs148567247 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | WWP1 | GRCh38.p7 | 8:86423116 | ATTGAATACCTAAAA[C/T]GTATTCAGACAAAAA | 11059 |
rs148582063 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86450899 | AGTTCTTCATAGGAC[A/G]TTATGTATTAGACTA | 11059 |
rs148588120 | in-del | -/A | 0.456803 | 0.140473 | intron-variant | WWP1 | GRCh38.p7 | 8:86358479 | ACACATTTATTGAGG[-/A]GTTTTTTTTTTTTTC | 11059 |
rs148651938 | snp | A/G | 0.00290342 | 0.0379905 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448474 | AGTTGGGAGGTTCCA[A/G]TATTCTGGTGACTGA | 11059 |
rs148677272 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86394564 | AAATGAGCAAAGCAG[A/T]GGTAAGGAGGTCTCC | 11059 |
rs148712957 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345880 | CTATTATATTACACA[A/G]TAAACTATTCCTGGA | 11059 |
rs148786372 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406682 | TGTGTGTGTGTTTCT[A/G]TACAGTTTTGTCACA | 11059 |
rs148800995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86418023 | AAGTGGATGAAGAGG[C/T]TAGAGAGCAGCTATA | 11059 |
rs148832275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86392957 | TATACACAAACGTAG[C/T]GTATGACAGCACCCA | 11059 |
rs148903326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420476 | GGGAAGGTACAACAT[A/G]TGTGTATATTTGGAA | 11059 |
rs148906739 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341844 | TGGGGGTTGGTCAGG[C/T]GGTTGGGCAAAAGCT | 11059 |
rs148927503 | in-del | -/T | 0.25334 | 0.249978 | intron-variant | WWP1 | GRCh38.p7 | 8:86457913 | CTGATTCTGTGCTCA[-/T]TTCCCAGGTTATGTT | 11059 |
rs148944432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86373442 | ATGGCCAATTTGTCA[A/G]TTTCTTCCTGTAGTT | 11059 |
rs148960478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86416385 | ATCTGCTGATGCAGT[A/G]GGTCAGTGGAGGGAG | 11059 |
rs148979073 | snp | A/C | 1.6531e-05 | 0.00287493 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466872 | TGCAATAGAAGAGAC[A/C]GAGGGATTTGGACAA | 11059 |
rs148988410 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86358032 | GTTTGATAGTTTGGG[G/T]GTTAGCATATGACTT | 11059 |
rs149043430 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86432643 | ACGGACTTTCGCTCC[C/T]GTTGCCCAGGCTGGA | 11059 |
rs149105634 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86453386 | TCCTTTTTTAGACTG[A/G]ATAATACTCCATTAT | 11059 |
rs149109232 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | WWP1 | GRCh38.p7 | 8:86354781 | GTGGAAGTATGGAAG[-/A]AAAAATATTGAGAGT | 11059 |
rs149113125 | in-del | -/CATATAGA | 0.466721 | 0.124627 | intron-variant | WWP1 | GRCh38.p7 | 8:86381078 | AAACCAAATTATTTC[-/CATATAGA]CATTTTCTCTGACTG | 11059 |
rs149116827 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86383947 | ACAGACTGGGTGCCT[A/T]AATGGAAATTGATTT | 11059 |
rs149171360 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86461500 | AGACAAAAATGAATG[G/T]GTCCTCATATAGCTG | 11059 |
rs149200495 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WWP1 | GRCh38.p7 | 8:86397916 | CATTGTCTCCATTTT[A/G]TAATTAAGAAACCAA | 11059 |
rs149270712 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414162 | GAAATATAGGCGAGA[A/G]TAGGAAATATTGGAA | 11059 |
rs149275487 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86463363 | CCAGTCTGGAGTGCA[A/G]TGGCACAATCTTGGC | 11059 |
rs149322653 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86407988 | TGAGAAATGCATATC[A/G]TCATGTACACACCAT | 11059 |
rs149359009 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86365148 | AATTAAAAATTAATG[G/T]ATTAACTCCCTCTGG | 11059 |
rs149377656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86349994 | GCAACCTGTCCCCCA[C/T]GCGCTCCAAGCCCCA | 11059 |
rs149435326 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86422656 | GGGATTACAGGTGTG[A/T]GCCACCACGCCCGGC | 11059 |
rs149437255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86344616 | CCTCTCAGAAGTCAA[A/C]TTCAAAGAGAGTAGA | 11059 |
rs149455539 | in-del | -/AAACA | 0.45574 | 0.142025 | intron-variant | WWP1 | GRCh38.p7 | 8:86465324 | CAAAAAGTAAAAAAG[-/AAACA]AAACAAAACAAATAG | 11059 |
rs149481948 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86375762 | TTCTTATGTCTGCTC[A/G]TGTATCAATAGGATA | 11059 |
rs149485423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86417341 | CCTAAGATATTTACC[A/G]TCTGGCTCTTTGTAG | 11059 |
rs149497629 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86440361 | TATTAAAGAGTTTAC[A/G]GGATTGATATATTCC | 11059 |
rs149533728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369628 | GTAATCTATGCCTCT[C/T]GCCTTTATTCTCAGT | 11059 |
rs149550983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86433967 | TCCTCTATCTCTCCT[A/G]CCTTACAAACAGTCC | 11059 |
rs149590615 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86390821 | CCCAATAGTCTACCA[C/T]ATCAGAATAGATTTT | 11059 |
rs149658848 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WWP1 | GRCh38.p7 | 8:86436123 | CAGCATCCCTTTGAG[A/G]TAGCACTTATTGTAT | 11059 |
rs149659036 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406445 | CAGAAGTACATGATA[A/C/T]CACAAGTTTATTATA | 11059 |
rs149685038 | snp | A/G | 0.00014845 | 0.00861411 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402152 | GTTGCTGCCAGACCC[A/G]AAAATACACCAGCTC | 11059 |
rs149739554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341821 | GGTGTGGACGTAGAT[A/G]TAATCTATGGGGGTT | 11059 |
rs149755978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86388526 | TTTTATGTTTCCCCT[A/G]GCACACTTTTTGATA | 11059 |
rs149793852 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86416225 | GAAGTGTGATAGAGG[A/G]CTCTTTGGAAGCATG | 11059 |
rs149806457 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86465778 | GACCTTGTTATCATA[C/T]TCTACCTTGAAGTAT | 11059 |
rs149846204 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86410065 | TAGATTTTCTAATGT[A/G]GTTTCCTAATATCAA | 11059 |
rs149869321 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86366691 | AGAGCTGTCTAGGCA[A/G]TTAGAGCCATTACAC | 11059 |
rs149912284 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86432304 | AAGCAATCCTAAAAG[A/G]TCTTTTGCAAAGTTG | 11059 |
rs149952411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86383561 | AGCCTGGCCAACATG[A/G]TGAGACCCTGTGTCT | 11059 |
rs150003704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86378004 | GAAATGCCACTGTTA[C/T]GCATTAGTATCTTGC | 11059 |
rs150006403 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86461406 | GACTTGATTGAACCT[A/G]AAGATTACTCTTCTG | 11059 |
rs150059284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86454622 | ACACCTAAATATTCC[A/G]TACCTCCAATTAAGA | 11059 |
rs150086332 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343266 | TCCTCCACCTTTCCC[-/T]TAACACCTCCCTGAA | 11059 |
rs150092097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385708 | AGACCACAAACAAAG[A/T]GGAATTAATGACCAA | 11059 |
rs150125445 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86392211 | TTTTTCTAGGCCAAG[A/T]TTGAGGCCTAGTCAA | 11059 |
rs150141573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86462784 | TGTGGTGCAAAAGCA[A/G]TGGTTTGTGAACCTG | 11059 |
rs150143935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86381233 | ACAAACAGTGTTACT[A/G]TGAAGTCTCAGTAAG | 11059 |
rs150181806 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86407564 | TGTCTTTGGCGGTGG[A/G]GAGAGCAGAATCTTC | 11059 |
rs150194913 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86457592 | ATATAGATGTGTGTG[C/T]GTGTGTGTGTAAATA | 11059 |
rs150233211 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | WWP1 | GRCh38.p7 | 8:86402486 | ATAGAGACAGAGTTT[C/T]ACTTTTTTGGCAACT | 11059 |
rs150259568 | snp | C/T | 1.6557e-05 | 0.00287719 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466830 | ACCATATAAGAGTTA[C/T]GAACAACTAAAGGAA | 11059 |
rs150281875 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86357177 | AAAATTATCAATATG[A/T]TCTATGTTCCAATTC | 11059 |
rs150333919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351702 | AACATGGCTGGCAAT[A/G]TATCAGCTAGTGATG | 11059 |
rs150335448 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468334 | TTTATTCAGAATTCA[C/T]AGTAAAGACGAAAGA | 11059 |
rs150368593 | in-del | -/A | 0.187685 | 0.242109 | intron-variant | WWP1 | GRCh38.p7 | 8:86439114 | TTGGGAGGCCAAGGC[-/A]GGGTGGATCATGATA | 11059 |
rs150390168 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369073 | CTAAGACTATAATTA[A/G]TAGTCAGACTTCATA | 11059 |
rs150440096 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402582 | ACAGGCATGAGCCAC[C/T]GCACCCAGCCTGTGC | 11059 |
rs150447303 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86444991 | CATGGTGCCAGCATC[A/G]TCTTCTGGTGAGGGC | 11059 |
rs150449308 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86364163 | TGAAAAGAGAATTGA[A/G]TTAAATAGCTTCACT | 11059 |
rs150495471 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86426977 | ACCATCCTGGCCAAC[A/G]TGGTGAAACCCCCAT | 11059 |
rs150499345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371824 | GAAGTCTCAGTTTCC[A/G]TGTAGTCAAAATATT | 11059 |
rs150596957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399620 | GCCTTCTGAATGTAT[A/G]TTTGGCTTAAGTACA | 11059 |
rs150648048 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86393994 | AAGCCCTGTGGCGGG[G/T]CACTGAGGTCTCCTC | 11059 |
rs150671796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86465498 | GGCCATGGTGGCATG[C/T]GCCTGTACTCCCAGC | 11059 |
rs150673078 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86382798 | CGTTGTCTGACACTT[A/C]AGTAGCTTGTAACAG | 11059 |
rs150689462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344322 | AGGGTTTTGAAAAGC[A/G]ATAATTATGAGCTAC | 11059 |
rs150724557 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86460438 | CTAGGCCTCCATTTC[A/C]TTATATGTACAGTGG | 11059 |
rs150768511 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86404822 | CTGTAATTGACATTC[C/T]GCTATCTGGCTGTTG | 11059 |
rs150804969 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86361443 | ACAACACTGTCAAAG[A/G]GGTTTTTCTAAAATA | 11059 |
rs150841032 | snp | A/G | 0.000345056 | 0.0131305 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438671 | TTATGGTGGCCTAGC[A/G]AGGTAAAATAAAAAA | 11059 |
rs150878560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86418836 | TCAAATACACACCCA[A/G]CACAGATCCCAGAAT | 11059 |
rs150946732 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86435932 | CTCAACCTCTGGGCT[C/T]GAACGATCTACCCAC | 11059 |
rs150965889 | snp | A/G | 3.29669e-05 | 0.00405984 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402130 | CACACCTTCATCTCC[A/G]TCTCAGGTTGCTGCC | 11059 |
rs150966036 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86356318 | TAAGTTTGGAACCCA[A/G]GTTTTAATGTTCTTA | 11059 |
rs151035211 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86457005 | AGGGGATGATGATTT[G/T]GATTACAAAAAGGGA | 11059 |
rs151035421 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86373834 | TAATGTTTATTTTTA[C/T]TTTTGCTTACTACTC | 11059 |
rs151036924 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86387738 | CATGTTAGCCAGACT[G/T]GTCTCGAACTCCTGA | 11059 |
rs151089127 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86451599 | TGGAGTTGAGGATAC[A/G]GGACAAAGAGGGTTT | 11059 |
rs151168868 | snp | C/T | 0.000164756 | 0.00907472 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461271 | GCGACTATTGCAGTT[C/T]GTCACTGGAACCTGC | 11059 |
rs151241822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86412517 | GCTTATTTAGTGATT[C/G]ACAGTTGTAAACGTG | 11059 |
rs151253512 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346549 | CTACTCAATTTTTTT[G/T]GGGTGGATTAAGTAG | 11059 |
rs151257507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86461635 | CAATTTTCTTCTTCA[A/G]GCAGAAGCAGCTTAC | 11059 |
rs151299736 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86406871 | TGTCATAGTTTTAAA[A/G]TGGAGTAAAAATGGT | 11059 |
rs151335168 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86363462 | TCCAAAAACAATGGC[A/T]TCCCATAAGTTTTTT | 11059 |
rs180730425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459997 | CACAGCTATTTTGTC[G/T]TATCCTTAGCTAAAG | 11059 |
rs180758491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428603 | TCAACCACATTTTTT[C/T]CAGAGGTTAAATAGT | 11059 |
rs180772068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450363 | TTACGCTAGTTGGAA[A/G]AAAACAGTAACACTA | 11059 |
rs180772562 | snp | A/C | 0.0665615 | 0.169854 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468442 | AAGAATTAAAAAAAA[A/C]ATTCTAATGTATGTG | 11059 |
rs180840759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86446314 | TTTTGAGAAGTGTCT[A/G]TTTATGCTTGCCCAG | 11059 |
rs180858120 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465337 | AAGAAACAAAACAAA[C/T]AGACCCAAAGAATTC | 11059 |
rs180887805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409344 | ATTCAAGCAATACTT[C/T]TGCCTCAGCCTCCTG | 11059 |
rs180913234 | snp | A/T | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86374888 | CTAATTTAAAAAAAA[A/T]TTTTTTTAGAGACAG | 11059 |
rs180923012 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86401270 | TTTAATAAAGTTATA[A/G]TAGTTTCAGGCCAGG | 11059 |
rs180938504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86383391 | GCCAAATGATCTTCT[A/G]GGAAGGTTGTAATGT | 11059 |
rs180940517 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424956 | TTTTTAAAATGTGGG[A/G]TATTCTCTTCCTTTT | 11059 |
rs180944836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365384 | GTTAGATAGGCATTT[G/T]TAGGCTTCAATACCT | 11059 |
rs180946477 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86346823 | ATACTTAATGGAGGA[A/G]AAATGATAAAAACAT | 11059 |
rs180954446 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86392970 | AGCGTATGACAGCAC[A/C]CATTTGTAAATATTT | 11059 |
rs180959100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86356480 | AAATCTTTGGTATTT[C/G]GTATAATATGCAAAC | 11059 |
rs181083751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360605 | ACACCTTTGCCTCCA[A/G]AATATATCTCTTTGC | 11059 |
rs181130176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459537 | ACTGGAAACAGTTCT[A/G]TAGAGGAGCTGAGCA | 11059 |
rs181140785 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441038 | AAAGTTAATTCTTCT[C/G]CCTCTTGCTAGTTAG | 11059 |
rs181155106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449945 | ATAGAGATCATTTAG[G/T]TTGTGTCCAGTTTGG | 11059 |
rs181157786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421442 | ATGGTTATCGTGTAT[A/G]AAAATAATTTAAAGA | 11059 |
rs181172939 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86406337 | CCACTTTGTTCCTCT[A/G]GTCATAACTTCTAGT | 11059 |
rs181180574 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86369852 | TACACTTGATGAGTT[A/G]GTGATTTATACTTTA | 11059 |
rs181186857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389547 | ATGGAGTCTCTTATG[G/T]CTACTTCTTTCTACA | 11059 |
rs181190489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86351659 | AAAGTTGCTAAAAGG[A/G]TAAGCACGAAATCTG | 11059 |
rs181245819 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86428210 | TTGCAGTATGCTACC[A/T]ATTCTGATTCTCTTC | 11059 |
rs181277559 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86396554 | GTCTTCTTTTATCAC[A/G]TGGTTTAAACATTTT | 11059 |
rs181293443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86392344 | AGAGTATATTCAGAA[C/T]TTCACTTTGTGTTTC | 11059 |
rs181294821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347309 | CTTTTTGGATGAATA[C/T]GCTGAGGCTAAAAAA | 11059 |
rs181296016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409035 | GGGGTTTTTAAAAAA[A/T]TTTTCTTGTGTATTC | 11059 |
rs181300254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86373803 | TCCTGTAGCAGGCAT[A/T]TCCAGGGCAACATTC | 11059 |
rs181314386 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86355874 | TGGGTTAGCTCAGCA[C/G]TTCTTATTTTATATT | 11059 |
rs181332957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412532 | CACAGTTGTAAACGT[A/G]TACAGTATATACAGT | 11059 |
rs181341003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86378764 | TGAGTATTTTGCCAA[A/G]TAAGGGTATTCAGTG | 11059 |
rs181363026 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86384275 | CACAATTCAGCCCCA[A/T]ACAAAAGGTAAATAA | 11059 |
rs181434133 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86464253 | AACTATTTATCTGTG[C/T]GGGGCTATAGATTAA | 11059 |
rs181437582 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WWP1 | GRCh38.p7 | 8:86446224 | TAACCTCAGGTGATC[C/T]GCCAACCTCGGCCTC | 11059 |
rs181522011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86455890 | ACCATAGTAAATAAG[A/G]TAGCGTGGTATTTGT | 11059 |
rs181522696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367755 | TAGTTTTTCTGTCTT[C/T]TCATATCCTGGGGAC | 11059 |
rs181596232 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86350424 | ATTAGTGCATAGCTG[C/T]GAAGCATTTTTGAAG | 11059 |
rs181600366 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429594 | TTTTTATGTATGTAT[C/G]AAAATATAAAAGATA | 11059 |
rs181609283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86414018 | AGATAAATGCTTCAG[C/G]AGACTTGTTGTCACC | 11059 |
rs181610672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86450906 | CATAGGACATTATGT[A/G]TTAGACTATGTCTTA | 11059 |
rs181621505 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86418109 | TTTTCAGTTGCTTTT[A/T]AAAAAAAACTTAGTC | 11059 |
rs181625550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86397809 | TATGTAGCATTTATC[A/G]AGCACTTATAAACTG | 11059 |
rs181633028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379819 | TAATAGTACCTGGCA[C/G]GGATGTTAATGGGCA | 11059 |
rs181702582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436207 | TGTGTATTTACTAAA[A/T]TAAAGCTTAAACAGC | 11059 |
rs181746491 | snp | A/C | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468625 | AGATTTGACTGAAGA[A/C]GGCAGCTTTCCAGTT | 11059 |
rs181754301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86440316 | TTTTATTTAATTCAT[G/T]TATTGGTGGGCTAGA | 11059 |
rs181755767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405831 | GCTACCATGTTGTCC[A/C]CTGCTACCTTTCTAA | 11059 |
rs181786903 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344713 | CGTGGTTTTGAAGGA[C/T]GATTATGACTTTGGA | 11059 |
rs181792925 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86369775 | AGTGTCTTTTTCTTG[G/T]AAGACTAAATGCTGT | 11059 |
rs181899965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455136 | CAGTAGTCATTCTTT[A/G]TGAAAACTCTTACCA | 11059 |
rs181903888 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417446 | AGAAATAAGATAACC[A/G]AAAGCAGTTCTGAAT | 11059 |
rs181906160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434709 | GGCATTTTTACCTAT[G/T]AATAAGTAATGCTGT | 11059 |
rs181911693 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86401812 | AACTTTAATATAAAA[C/T]ATGTCATATCTTTGT | 11059 |
rs181930898 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86459050 | TTTTTTTTTTTTTGA[A/G]ACAGAGTCTCACTCT | 11059 |
rs181998392 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86396775 | ATTTTTAATTTTTTT[A/T]AAAAAATAGAGACAG | 11059 |
rs182009285 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86379236 | AGAGCAGTTTGGAAC[A/G]ATGAAGGATGGAAAT | 11059 |
rs182014607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362379 | GTTTATTGAGTGATT[C/G]AATTGTAGTCTTATG | 11059 |
rs182023663 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86420626 | AGGAAGTTAATAAGT[A/T]AAAGAAGTAAATACC | 11059 |
rs182026521 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344059 | AATGCACCTTTTAAA[A/G]AAGAAAGTCGTTCTT | 11059 |
rs182029168 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86361359 | TCTGCTCCTCAATAC[C/G]TCTGCTGCTTCTTCT | 11059 |
rs182039699 | snp | G/T | 0.00482189 | 0.0488641 | intron-variant | WWP1 | GRCh38.p7 | 8:86425334 | GTAATATAGCACTCT[G/T]TATGCATTTGTAATT | 11059 |
rs182039990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86465995 | CACCTGGATAATCTC[C/T]AGAAACCTTCCACAT | 11059 |
rs182040137 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388605 | ATCTGTTTGGTCTGT[A/G]TTCTGGTTTTGATTG | 11059 |
rs182081916 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415080 | TGTACAGTTCCAGAA[A/C]TGAAGAAGAATATTC | 11059 |
rs182088008 | snp | A/C/G | 0.00637247 | 0.0561273 | intron-variant | WWP1 | GRCh38.p7 | 8:86443442 | TTTGGAATTTTAAGC[A/C/G]CTTTGCAGAAGCCCT | 11059 |
rs182095128 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367597 | TATACAATTCTGTGG[G/T]ATTTTCAAAGGGTTG | 11059 |
rs182099063 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86399055 | AAATGGATTCATATA[A/G]TATGTGACCTTTTGT | 11059 |
rs182109888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86382218 | AAATTTAACAATATA[C/T]CATAAATATTAAGTT | 11059 |
rs182109889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86421814 | GGGGACAGAGCGAGA[C/T]GCCATCTCAAAAAAA | 11059 |
rs182115391 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86363750 | GCAGTGAGCCGAGAT[C/T]GCACCACTGTACTCA | 11059 |
rs182116309 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345422 | AGCTTTTTTTATTTT[C/T]GAGGCAGGATTTCTT | 11059 |
rs182197039 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86347015 | TTTTATTTTATTTTA[C/T]TTATTTATTTTTGAG | 11059 |
rs182205465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418520 | ACCTCACTTAGCAAA[C/T]CCAAGAGAGCTGGAT | 11059 |
rs182214487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86436802 | GATGAACCAAATTAT[A/G]CTGTGTACTCAGGCA | 11059 |
rs182216249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403592 | GAGCCACCGTGCCTG[G/T]ACAGTAATAAGTCTT | 11059 |
rs182226752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86413428 | ATCAGCCAGCATACA[A/G]TACAATTAAAGCTAT | 11059 |
rs182227539 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367889 | CTCTCATTCTGTTCA[A/C]CATTTATTCCAAAAT | 11059 |
rs182228796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384878 | TTTATCAAAGATACA[A/T]AAAATTAGCCAGGCA | 11059 |
rs182243654 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86347625 | TTAAATTTGTAAGCA[C/T]TGTACCACAGAATAG | 11059 |
rs182289689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349458 | TGGGGCCACCCATGT[A/T]ACAGATTACCATAAA | 11059 |
rs182332660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447190 | AGGTACAGGCATTGA[C/G]TAACCTGAGAGTTGA | 11059 |
rs182351995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409589 | AATAGGCTGGGCACA[A/G]TGGCTCATGCCTGTA | 11059 |
rs182376833 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86383697 | AGTGAACTGAGATTG[C/T]GCCACTGCACTCCAA | 11059 |
rs182383661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453087 | TTAAAATATACCATC[A/T]TAACTATTTTTAAGT | 11059 |
rs182440264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466697 | CATATATAGTATACA[C/T]ATATCCATTCAGCAT | 11059 |
rs182458423 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | WWP1 | GRCh38.p7 | 8:86389977 | CTCCTCACTTCTCAG[A/G]CGGGGCAGCCCGGCA | 11059 |
rs182578107 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377341 | GACCACAGGTGATCC[A/G]CCTGCCTCGGCCTCC | 11059 |
rs182596994 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86462103 | GTAAGATGTAAGTAT[C/T]CCCTGTTTTTTATGA | 11059 |
rs182601060 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341957 | TATTTGCACATTGGC[C/T]TTTCTTCTAAAAGCA | 11059 |
rs182601228 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86423441 | CTTAAGGAGTATGCT[A/G]CCTTCAAGCATCTGT | 11059 |
rs182604771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86444725 | GGTAGGGTGGAAAGA[C/T]TGATGGGAGTAAAAT | 11059 |
rs182619665 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86407868 | GTGATGTTTGTTACA[A/C]TTAATGAACCATTAA | 11059 |
rs182619922 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86371143 | TCCACCTTTGGGAGG[C/G]ATCTCAGCCTCCCAA | 11059 |
rs182643956 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86354088 | GGTGTTGGCACCCAT[A/G]GGCTGAGTGCTACTG | 11059 |
rs182691349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406672 | TGTGTATGTGTGTGT[A/G]TGTGTTTCTATACAG | 11059 |
rs182761982 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86410966 | ATTTTTATAGTGACA[C/T]GTAGTCGAACTAGAT | 11059 |
rs182857893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86394114 | AGTTTCAGAATAATT[C/T]GTTACTCAGCAATAG | 11059 |
rs182864489 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86358566 | AACTCACCACTGCCT[A/C]AAGTTCCCCAGGCTC | 11059 |
rs182885679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466369 | AATTCCATGAAGACA[A/G]GGATTTTAGTTTTCT | 11059 |
rs182915690 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86410341 | TTCATCACCTTTTCC[A/G]TTGCTGCTCTGATTT | 11059 |
rs182918909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86447558 | AGTGTGAGCCACTGC[A/G]CCCCACCTTGAAGGT | 11059 |
rs182921570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426001 | ATTTCCCTTCCAGAT[C/T]CAATTTAAAGCCCAC | 11059 |
rs182929374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393663 | TTAGAAAACTTTGCT[A/G]TTATTAAGACTGTCA | 11059 |
rs182932879 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368681 | CTCTCTGTTTGCCTG[A/G]TCACGTTACACTGTC | 11059 |
rs182934506 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430057 | TACAAATATTAGCCG[A/G]GTGTGGTGGCGCATA | 11059 |
rs182945390 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86376657 | TGAAAGACTATCAGG[C/T]GACTCAAATCTGGAG | 11059 |
rs182954600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86398108 | CACTTATTATTTAAA[G/T]GTATTTATATGTTCT | 11059 |
rs182971240 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86363273 | TTAAAGCAGAGGGGA[A/T]TTCCTTATTATGTTG | 11059 |
rs183013442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453316 | TGACTGGGTTATTTC[A/C]CTCAGCCTAATATCC | 11059 |
rs183024023 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WWP1 | GRCh38.p7 | 8:86426958 | CTGAGGTCAGGAGTT[C/T]GAGACCATCCTGGCC | 11059 |
rs183026151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456392 | AACAAAAAAACTCAC[A/G]TAACTCAATAAAAAG | 11059 |
rs183026759 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86432504 | TTTTATTTCTCTACA[A/C]AATTATTCTTATCAG | 11059 |
rs183052306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370769 | AGAAGGTGTTAATGC[G/T]CAGAACTCATCTGTC | 11059 |
rs183058711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353404 | TATGTTAGTAATTTT[A/G]TGGTCAAAAATATGC | 11059 |
rs183111629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358112 | TAAGCTTCTCTCTTA[C/T]ATTCTTTTGTTTCTT | 11059 |
rs183155866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457153 | CTCAAAGTTGACTTA[C/T]GAAAAAAACTAAGAG | 11059 |
rs183160659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86437924 | CCTGCCTTAGCCTCC[C/T]GAATAGCTGGGACTA | 11059 |
rs183177542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86419087 | TCTTAATTTGAAAGA[C/T]AGAGATCAAAAAAAC | 11059 |
rs183183008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86451837 | TTTTACAGATTTTGT[A/G]TCACTGACAGATTTT | 11059 |
rs183219231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414489 | GTGGAACCAAGGTGG[A/C]TTCTTCTGGCATACA | 11059 |
rs183230058 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WWP1 | GRCh38.p7 | 8:86380325 | AGAGACAGAGAGTAG[A/G]TTAGTGGCTGCCTAG | 11059 |
rs183256627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344963 | GATTTTGAATTGGGA[A/G]TGAAACAATTTGAAC | 11059 |
rs183274810 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86457659 | GATACATGCTTTTCA[A/C/G]TATAGCTGTTTTTCT | 11059 |
rs183298483 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86419322 | ACTCAGAAGGCTGAG[A/G]CAGAAGAATCGCTTG | 11059 |
rs183338778 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86375426 | TCTCTCCCTTGCCCT[A/G]TAGGTTCACATTTTT | 11059 |
rs183357773 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86357929 | GCTTGGTGTTGGTAT[C/T]CTACCACCATTTGTC | 11059 |
rs183376660 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341038 | TAAGAGCTTCTGAAC[A/G]GGGAGGAAATTGAGC | 11059 |
rs183434291 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86407239 | CCTGTCCTTCCTCTT[C/T]CCTTTTCCTTTCCTT | 11059 |
rs183490470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438474 | AGTTAAAAGCATTGT[A/G]TAAGATAAGGAAATG | 11059 |
rs183511446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404712 | AACTGATTTATCTCT[C/G]TCACAGTAACTCCTT | 11059 |
rs183597306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434626 | GAGTGATAAGACATT[C/T]GTACTTTACTTATTT | 11059 |
rs183603798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86463292 | TTCCTCGATGAGATT[A/G]GTGGGGTTTTTTGTT | 11059 |
rs183614488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416671 | GACCATACCTAAACA[C/G]TAGGTAGAAGAGGGT | 11059 |
rs183614731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454908 | TAAGAGTGCTAATCA[A/G]TTAAGAGTGCAGAGC | 11059 |
rs183620680 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86444276 | ATGGCCAGCTTGTCT[C/G]GTTGCAAATTTTGGG | 11059 |
rs183624803 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WWP1 | GRCh38.p7 | 8:86401296 | CCAGGTACAATGGCT[C/T]ACACCTATAATCCCA | 11059 |
rs183646399 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366116 | GATGCCGGAGAGTGC[A/T]GGAGAGACTGTAGTT | 11059 |
rs183647677 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WWP1 | GRCh38.p7 | 8:86383562 | GCCTGGCCAACATGG[C/T]GAGACCCTGTGTCTA | 11059 |
rs183664414 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346842 | TGATAAAAACATACA[A/C]AGATGAATTTTATTG | 11059 |
rs183699149 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86390056 | CCTCAGATCCCAGAC[A/G]GGGTCGCAGCTGGGC | 11059 |
rs183776621 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WWP1 | GRCh38.p7 | 8:86349034 | AGCAACCAGATCTTT[C/T]TTTTTGAGAGGGAGT | 11059 |
rs183813890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86404075 | TCAAATCTGAAATGC[C/T]CCAAAATCTGAAACT | 11059 |
rs183815790 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368280 | GGAAAAGTTAACTTG[A/G]TCATACAGCTCTTAA | 11059 |
rs183848970 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86422524 | GTGCCACCATGGCTG[C/G]CTAATTTTTTTTTTT | 11059 |
rs183852742 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86460835 | TTTTTTTTGAGACAG[A/G]GTCTTGCTCTGTCGC | 11059 |
rs183941914 | snp | C/T | 3.30415e-05 | 0.00406444 | intron-variant | WWP1 | GRCh38.p7 | 8:86457891 | TTCACTAAATCTTTA[C/T]TGTGGCCTGATTCTG | 11059 |
rs183945076 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86419755 | AATCCAGGATGATAA[A/C]TGAAAACAGATCTAT | 11059 |
rs183958620 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86405044 | CAGAGGCTTCCGGAA[A/C]CTGCTCTGTTGGTAG | 11059 |
rs183964094 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368850 | AAGGCTGGATTATCT[A/G]CTTTCTCTTGTGTGC | 11059 |
rs183968458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386985 | GGACAGAAAAGGGCA[C/T]ACCCACTCACTCAAG | 11059 |
rs184000101 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86385433 | ACAATCTAGCTCTTC[A/G]GGAAGAACCCGGGAT | 11059 |
rs184012962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352326 | CCCTCCCAGTTTCAA[A/G]TGATTCTTGTGCCTC | 11059 |
rs184019858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347850 | TTTCCAAAATATATA[C/T]AGATTGGGTATCCCT | 11059 |
rs184035999 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86446227 | CCTCAGGTGATCCGC[A/C]AACCTCGGCCTCCCC | 11059 |
rs184057331 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86465011 | AAGTAATTACCACCC[A/T]CTGATTTCTGTTTTC | 11059 |
rs184059822 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86409085 | TCATTTTCACTACAA[A/T]TGAGTTTTACCATAT | 11059 |
rs184064055 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86424700 | ATCGCAGGCACTCGG[C/T]AGGCTGAGGCGGGAG | 11059 |
rs184110277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346595 | AAAGTGTAGTGCGAT[G/T]GGTAAACAGTTGACT | 11059 |
rs184157588 | snp | C/T | 0.187053 | 0.241946 | intron-variant | WWP1 | GRCh38.p7 | 8:86423889 | GACGGGGCGGCTGGC[C/T]GGGCGGGGGCTGCCC | 11059 |
rs184161148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370077 | TACCTTTTCCCAGCC[C/T]CTAAAGTAAGTGCTA | 11059 |
rs184166398 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86390707 | GAGACGAGAGGGAGA[C/T]GGGAGAGGGGGAGGG | 11059 |
rs184171306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354779 | GTTGTGGAAGTATGG[A/G]AGAAAAATATTGAGA | 11059 |
rs184173016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449118 | AATGCTGGGATAACA[A/G]GGTGTCACCATCCTG | 11059 |
rs184184991 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467468 | TGTTTTAAATAAATA[C/G]AATAGTTGAAAATTT | 11059 |
rs184197788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427334 | GCAAACGACCATGGC[A/G]CATGTATACCTGTGT | 11059 |
rs184202003 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86396296 | TGTAGAGACGGGGTT[C/T]CACCACGTTGGCCAG | 11059 |
rs184284353 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86408616 | TTTAGTAATGTTTTT[A/T]AAAGTGTTTTCTTCA | 11059 |
rs184286977 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86445470 | TGGCTTGGGAAAATG[A/G]CCTCCATCTGCATCT | 11059 |
rs184321498 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86371749 | TTAGTTTTTTGTTTC[A/G]CAAATTTATTCCAGT | 11059 |
rs184423228 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348541 | ATTTCTTAAATCTAC[A/G]GTTCACTCACAGCAC | 11059 |
rs184477397 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86450048 | TAGATTTTTAAAAAG[C/T]GAAGTTACTGGGTCA | 11059 |
rs184485924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86408819 | GGAGGCTGGGGCAGG[A/G]GAATTGCTTGAACCT | 11059 |
rs184494098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372494 | TGTCTCTTAAGAAAT[A/C]CTTCCATCCTGAGAG | 11059 |
rs184494352 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415773 | AGTAGGCTTCTTCTA[A/G]TCAGCATGATGTAAC | 11059 |
rs184496426 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391936 | CAGAGGAAGGATTTA[A/C/T]CATTGTAAGCCGTTT | 11059 |
rs184506885 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WWP1 | GRCh38.p7 | 8:86412978 | GGATTAGAGGCACCC[A/G]CCACTATGCCCAGCT | 11059 |
rs184509290 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86399524 | ACAAAGTGTGACTTT[A/T]ATTAATCTATAGTTA | 11059 |
rs184514271 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86355349 | TTCTGAGTAATTCTC[G/T]TAATCACCTCTCATC | 11059 |
rs184519545 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86378830 | AAGAGTTAATACTAT[A/G]TAGTCAGTAATAATA | 11059 |
rs184620478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428460 | TACTGGACAACTACA[G/T]ATAGTGTTTTGAGGC | 11059 |
rs184622422 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468107 | TTTTAGCAAACTGGG[C/T]TTCCTAATACAAAAT | 11059 |
rs184624815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395901 | AAAGAATTTACCAAG[A/C]AATACACACTAAAGA | 11059 |
rs184632088 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86411386 | TTTATTTTATGTTAC[A/G]TATTTTGAAAATATT | 11059 |
rs184636827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377607 | CATTGATCATGGAAC[A/G]CGGAAAAACTGATGG | 11059 |
rs184648535 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86400364 | ATAAATAAAGATAGT[A/G]AACAACAGAAGACAT | 11059 |
rs184653240 | snp | A/C | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342225 | TAAATGCAATTATTT[A/C]CTCTTGCAATGTGTT | 11059 |
rs184655516 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86396622 | TTTTTCAGACAGGGT[C/G]TCGCTCTATTACTCC | 11059 |
rs184657428 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86359608 | AAGCATTCTTTTCTC[C/T]TCCAAATCTCAGAGT | 11059 |
rs184658164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360966 | CCTTTGCAGCATTCA[A/G]GGTAATTAGGTTGAG | 11059 |
rs184682637 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86365120 | CTCAGAAAAAAATCT[A/G]TGTATTAACGTTAAT | 11059 |
rs184803858 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86416101 | AGGCACTCATTGAAC[G/T]TAATTACAAAGAGTT | 11059 |
rs184806497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383290 | TTATTTAACCATATT[C/G]CCATTGTTGGACATC | 11059 |
rs184859394 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86433681 | TGTTATGGTGGCTCA[C/T]GCCTATAATCCCAGC | 11059 |
rs184888475 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86384938 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG | 11059 |
rs184972645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458188 | AACACTTGTTAAAAG[C/T]ACTTTCTATTGCTTC | 11059 |
rs184984457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86454257 | TGCAATGCAAATGCT[A/G]TGGTAAATAGTTGTT | 11059 |
rs185005041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439535 | TGTACAATATTCTGT[G/T]GTATGGAAATATCAT | 11059 |
rs185029611 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360196 | AACATCTTTTACGCT[A/T]ATGTTTCTCTTTGAT | 11059 |
rs185036655 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86456548 | TAGTGTTGGTAGTTT[C/T]TTGTAATGTTAAATG | 11059 |
rs185043031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437171 | GCTGTGCTCCAACCC[A/G]GACTTGCCAGTCTTG | 11059 |
rs185057755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418665 | ATTCCCTTCCCTGCA[A/G]CCAGAACTTCTGCTC | 11059 |
rs185075927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403593 | AGCCACCGTGCCTGG[A/T]CAGTAATAAGTCTTA | 11059 |
rs185139825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378393 | TGTGACTCTTACTTA[C/T]TTCTTAAGTTTATTA | 11059 |
rs185149007 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86459155 | CCGCCTCAGCACCCC[C/T]ACTCCAAGTAGTTGG | 11059 |
rs185156368 | snp | C/G | | | utr-variant-5-prime, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342770 | GGTTCCGAGTGGCTG[C/G]TGGCGGCCTGGGCTG | 11059 |
rs185175913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459603 | AATAAAAGCCTTTTG[C/T]ATTCTATACTATTAC | 11059 |
rs185179734 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86382860 | TAAATATTTTTGCTC[G/T]TCTTATTTCTGTAGA | 11059 |
rs185181682 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86442239 | AAAATGAATTAATAT[G/T]GTGAGGTTGTTACAA | 11059 |
rs185184116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345588 | CTAATTTTTGTATTT[C/T]TTTTTTAGAGATGGG | 11059 |
rs185201421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86421546 | TATTTGAAAATAGGC[C/T]GGGCATGGTGGCTCA | 11059 |
rs185212067 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86389778 | GATGGGGCGGCTGCC[C/T]GGCGGAGGCCGCCCC | 11059 |
rs185218576 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86406475 | ATTTTTTTCTTAGCT[C/G]TTTATTCTGAAGTAA | 11059 |
rs185218817 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86369978 | AATAATAAAAAACAT[C/T]TGGGAACCAACTGCT | 11059 |
rs185288046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363938 | ACATTTTCCTTGAAA[A/G]GGTGGTTAGTTAGTT | 11059 |
rs185305366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445652 | GGTAGCACAATTTAT[C/T]TTCCTCTGGATATCT | 11059 |
rs185377212 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86374518 | TGGTACTCATTATAT[A/G]AATTTAGTTATTTCT | 11059 |
rs185417440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463932 | CGGGTGTGGTGGCAC[A/G]CACCTGTAGTCCCAG | 11059 |
rs185442566 | snp | C/T | 0.105924 | 0.204309 | intron-variant | WWP1 | GRCh38.p7 | 8:86424589 | TGGCAGATCACTCGC[C/T]GTTAGGAGCTGGAGA | 11059 |
rs185463061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86427269 | ATTAGGGCTAATGCT[C/T]TCCCTCCCCGTAAGG | 11059 |
rs185480193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369472 | GAAAGGGTTTATATA[C/G]AATAAAGAGAAAAAT | 11059 |
rs185499956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344011 | AAATCCACTTTACCT[A/G]CCTCACCAAATCTGT | 11059 |
rs185559271 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86392614 | AAATACAGCAGAGAA[A/G]TGTATCATTTGTGGT | 11059 |
rs185567752 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86347341 | AAGTTTAAAAAGTTA[A/C]ATTTCCAAAGTATGT | 11059 |
rs185567969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367757 | GTTTTTCTGTCTTCT[C/T]ATATCCTGGGGACCA | 11059 |
rs185589258 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86387646 | GCCTCCTGAGTAACT[A/G]GGGTTACAGACGTGT | 11059 |
rs185618890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86349567 | CAGCTTACTACTTTC[C/T]GCAAATCTGGATTTT | 11059 |
rs185629286 | snp | A/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467108 | CCAGGAAAAAGATCA[A/T]CCTTAAATTTTGAAG | 11059 |
rs185643648 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86405399 | TGAAAGGCTATTTAT[C/G]GTTCTTATTTATCAT | 11059 |
rs185698607 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86369800 | TGCTGTCTGAAAGCT[C/G]TATCTGTCCTTCTTT | 11059 |
rs185706531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389367 | ATGACTCTTAACGAG[C/T]ATGCTGCCTTCAAGC | 11059 |
rs185716499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86351246 | AAGTTGAAAATTCAA[A/G]CAAGTATTCACTTTG | 11059 |
rs185779228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393041 | AAGCATTTCTTTGAT[C/T]ATTAATAAGGTCAGA | 11059 |
rs185781486 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86357853 | CATACCTCCATGGAA[C/G]GATAGTTTTCCTTGT | 11059 |
rs185782910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420276 | GCTAATGAGCTTGAA[C/T]GTTTTAAGAGGAGAT | 11059 |
rs185889597 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WWP1 | GRCh38.p7 | 8:86409546 | GCCCTGATTTTACTT[C/T]ATTCTTGATCTTAAT | 11059 |
rs185918382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374978 | CCACCCTCCCAAATT[C/G]AGCCACTGTGCCTGG | 11059 |
rs185951460 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86465487 | AAAAGTTAGCTGGCC[A/G]TGGTGGCATGCGCCT | 11059 |
rs186053373 | snp | C/G | 0.00186741 | 0.0304995 | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468737 | ACCAGCTTTGTTTTG[C/G]AGAATTCATCAGGGT | 11059 |
rs186060099 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86446948 | TTCTTCTGGTTGCTT[C/G]TGTTTCCTCTGTGAA | 11059 |
rs186084266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86451397 | TAGGTTTAAAATTAC[C/T]TTGGTTTACAATTTG | 11059 |
rs186084627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414092 | TGTTTTTCAAATTGT[A/G]GAGTGCAACCCGTTA | 11059 |
rs186093427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429823 | GTAAAGTATTGATGC[C/T]AGTGTATTATTTTTA | 11059 |
rs186118912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351880 | GATCTCTGATATGGT[C/G]CTTGAGAGTGGAGCT | 11059 |
rs186208214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425591 | TTTTAAGGAAAGAAA[A/G]GTAGTATTTAGGACA | 11059 |
rs186216895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393431 | TTTTGTGTTCTTAGT[A/T]GAGGCAGGGTTTCTC | 11059 |
rs186227307 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WWP1 | GRCh38.p7 | 8:86409602 | CAGTGGCTCATGCCT[A/G]TAATCCCAGAACTTT | 11059 |
rs186229676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455663 | TAAGGAAGACCTAAA[C/T]AAATGAAGAGATATA | 11059 |
rs186231442 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86375808 | ATTGCTGGGTCAAAG[C/G]GTAGACACATGTAAT | 11059 |
rs186237212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451857 | TGACAGATTTTCTTC[C/T]TTATTTCCTTTCTGT | 11059 |
rs186237748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434827 | AGAACATTTTTCATC[C/T]GTTCCAAAGTGTTCC | 11059 |
rs186251748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86357948 | CCACCATTTGTCACA[A/G]TGTTTCTGTGGGAAA | 11059 |
rs186257664 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340919 | ATAAGGACATGAACA[A/G]TGGTTATGGAATACT | 11059 |
rs186306503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460145 | TGAAAATAACCAGTC[A/C]ATGAAATAGATAATT | 11059 |
rs186365387 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | WWP1 | GRCh38.p7 | 8:86361989 | GTATATATATATATA[C/T]ATACATATATATACA | 11059 |
rs186365590 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344232 | GTATGTGGAATAGTT[C/G]TTTGGGACATAGCTT | 11059 |
rs186405412 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86402790 | AAAAAATACTATGTA[A/G]TTCATGATATAAAAT | 11059 |
rs186408313 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86436283 | AATTTATTACCTCAA[A/G]GTTTTGATAATGCTA | 11059 |
rs186430329 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86356039 | GACTAATAATGATGA[C/G]TCTAATGGATAATTG | 11059 |
rs186459655 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367926 | ACTGTGAACAAGCCC[A/G]TTGTCTTCCATGGAA | 11059 |
rs186459679 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342200 | AAAGTCTTCGGGTAT[A/G]ACCAATGGCTAAATG | 11059 |
rs186471018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347672 | GATAAAGCAAAAGTT[C/G]ATTTCTTATCTGGAA | 11059 |
rs186478514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429149 | TGGGCCTCACATCCA[C/T]AGTCTAGGCAAGAAG | 11059 |
rs186501501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396979 | GTGATCCTCCTGTGT[A/C]GGCCTCCCAAAGTGC | 11059 |
rs186505798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86413514 | AGGAGTTACCTGCGC[C/T]GTTGACGTCAAAGAA | 11059 |
rs186513601 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86379321 | TAATTGCTATGTTGC[C/T]GGTACTTAAATATAG | 11059 |
rs186537871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420662 | AATGGACTGAAACAG[G/T]TGAAAATGTTGCCTT | 11059 |
rs186542622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398018 | CTTAATCTGACTCTT[A/G]TGCAGAAATTTTGCC | 11059 |
rs186548208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86362761 | CAAGGACTCAATGCT[A/G]GACAAGATCGAGTGT | 11059 |
rs186591310 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456080 | AAAATTAACTATAAG[C/T]CTACCTCAGTCCATA | 11059 |
rs186643762 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86418350 | TGTGTATTATTTATT[A/G]CTATATAATAAATTA | 11059 |
rs186650827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86384456 | GTCAAGAGTATACAC[A/G]TAATTTCCGGGTTGT | 11059 |
rs186780414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86440447 | AGATATAAATTTCTC[A/G]CACACTTGTTTTTCC | 11059 |
rs186782384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86406215 | AATTTATGAAAAGAG[A/G]ATAATATGCGACTAC | 11059 |
rs186783439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363519 | AAATTATATGTCTAT[A/G]GGCCGAGCATGGTGG | 11059 |
rs186786555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86380089 | TTTATGCACAATAGC[C/T]ACAAAGTGGAAGCAG | 11059 |
rs186791265 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344906 | GTTTTTAATGCCAGA[A/C]TTATGACCTTGGATT | 11059 |
rs186791569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345062 | TAGAAAGACCTCCCA[A/G]TTGTTGTAGTCATGG | 11059 |
rs186891048 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86390632 | AGGTTGCAGTGAACC[A/G]AGATGGCGGCAGCAC | 11059 |
rs186899408 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | WWP1 | GRCh38.p7 | 8:86447383 | GCAATTCTCCTGCCT[C/T]ATCTTCCTGAATAGC | 11059 |
rs186902409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408068 | TTTATCCCTCAAACC[C/G]TTTGCAACAGCTGTT | 11059 |
rs186923393 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86417762 | AAATACAATATTTAA[A/G]TCATATAGAAATATT | 11059 |
rs186933627 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86384043 | CTCTCTTCTTGGCTT[A/G]TAGATGGACATCTTT | 11059 |
rs186957286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347066 | CCAGGCTGGAGTTCA[G/T]TGGCACAGTCATGGC | 11059 |
rs187039830 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86462699 | TAGAGATAGGTGATT[A/C]TTTCAAGAGGTCAAA | 11059 |
rs187069737 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86423752 | GTACACTTCCCAGAC[A/G]GGGTGGCGGCCGGGC | 11059 |
rs187070904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86445423 | AATGCTGAGCTCCCA[C/T]CTGTACGTAAGAACA | 11059 |
rs187088578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465996 | ACCTGGATAATCTCT[A/G]GAAACCTTCCACATG | 11059 |
rs187132881 | snp | C/T | 0.00445358 | 0.0469783 | intron-variant | WWP1 | GRCh38.p7 | 8:86402014 | TAAGGCATTTTTTTT[C/T]CAAGGTTGGCTGTTG | 11059 |
rs187134554 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367703 | TTTTTCTTTTGCCAA[A/C]CCTGCTTTCTAAATT | 11059 |
rs187181459 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86466430 | AAAAATTCTCGGTAA[A/T]TGACTGATGAATGAG | 11059 |
rs187198138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86404925 | TTCATCTTTTATACT[A/G]CTAGGCTTCACACAG | 11059 |
rs187204574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410378 | TTTTCTTTCCCTTGA[C/G]TTAGTTTAGCTAATT | 11059 |
rs187209439 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86448065 | GTTTACTTGTGAAGT[C/G]TCATGATTTTTCTTT | 11059 |
rs187210143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443840 | GCTCTAATGTGGGAG[G/T]GCATTCTTGATTGAG | 11059 |
rs187213316 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468486 | TAGAGGGAAACTGGC[A/C]TTCAAAAAGGACTGC | 11059 |
rs187221866 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86426217 | AGATCATCAAGTTAT[A/G]GTCATTCATTTAGTC | 11059 |
rs187223266 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86386331 | AGAGGATCTCTTGAG[G/T]CCCAGAGTTCAAGGC | 11059 |
rs187228221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368716 | TGTTCCATTGTCCAC[C/T]ATGCAAGCAGTTCTC | 11059 |
rs187231914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348835 | AGCAAACAGCCCTAA[A/G]CCAAGTGACTTAAAA | 11059 |
rs187232562 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86406999 | TCATGTGAAACTTAA[C/G]CTCTCAAAGATTAAA | 11059 |
rs187300308 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86370568 | GAGGCTCAGGATCCA[C/G]AGTACCCCACATTTC | 11059 |
rs187306495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453927 | CTATTTTAACTGCAG[A/C]CATCTTGGGCCTTTT | 11059 |
rs187311908 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86432641 | AGACGGACTTTCGCT[C/T]CTGTTGCCCAGGCTG | 11059 |
rs187346744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353594 | ATCTCCTGGGTTCAC[A/G]CAATTCTCCTGCCTC | 11059 |
rs187474249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86378127 | CTTTTATTACTTTGC[A/G]TTTTAAAATACACGT | 11059 |
rs187498307 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86450858 | GTGGGAAGAGAGCTA[A/T]TGTTTCTGCTGGGAG | 11059 |
rs187498417 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86389978 | TCCTCACTTCTCAGA[C/T]GGGGCAGCCCGGCAG | 11059 |
rs187504566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407278 | GGTTTTATCTGTTCA[A/G]TCTTTCTTATATCCA | 11059 |
rs187506576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86352624 | CTCACCTTGCCCTCT[C/T]TCCCAATGTGCTGGG | 11059 |
rs187510455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86370958 | GCAACCTCTGCCTCC[C/T]GGGTTTAAGTAATTC | 11059 |
rs187513495 | snp | G/T | 0.180383 | 0.240111 | intron-variant | WWP1 | GRCh38.p7 | 8:86390217 | CTTCCCAGACTGGGC[G/T]GCCGGGCAGAGGGGC | 11059 |
rs187543173 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466900 | CAAGAATGAATGTGG[C/T]TTCTTATTTTGGAGG | 11059 |
rs187560115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427061 | CCAGCTACCCAGGAG[G/T]CTGAGGCAGGAAAAT | 11059 |
rs187585023 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86394316 | ACACTAAGGAAGAAG[A/G]TCTAGGAGGTACAAA | 11059 |
rs187585360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86358946 | GAAGACAAATAGCAA[C/G]TAGTTCAAAACTGGA | 11059 |
rs187601998 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86449042 | ATAGGGTCTCACTGT[A/G]TTGCCCAGGCTGGTC | 11059 |
rs187635064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427270 | TTAGGGCTAATGCTT[A/T]CCCTCCCCGTAAGGG | 11059 |
rs187638271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395958 | TCTATTCAAACAGCT[A/G]TATATTTTAGGGAGA | 11059 |
rs187645720 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457189 | GTATTACATATTTTA[C/T]TATACCTAAAATAAT | 11059 |
rs187647241 | snp | C/G | 1.6574e-05 | 0.00287867 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411769 | ACACCTCTAATTCTA[C/G]AAGTAGTTCTGCTTT | 11059 |
rs187698900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86414750 | ACATTTTTTAATTCA[C/T]TTTATATAGAGATAT | 11059 |
rs187703237 | snp | C/G | 0.000317281 | 0.0125913 | intron-variant | WWP1 | GRCh38.p7 | 8:86380676 | ATTGATTAGTGTGCA[C/G]TACTACTTTTTGGCA | 11059 |
rs187709058 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86354155 | TATGTAAACTGAGAA[G/T]AATATACCCAATTCA | 11059 |
rs187760193 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86453131 | AAATATATTCACATT[A/G]TGCATCCAATCTCCA | 11059 |
rs187796002 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86431041 | ATGTATATTATATAT[A/G]TATATATTATAAGGG | 11059 |
rs187798127 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86399269 | CATGAGAAGATAAAT[G/T]CTTCACAGATTGTGG | 11059 |
rs187810777 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WWP1 | GRCh38.p7 | 8:86363810 | AAAAAAAAAAAAAAA[A/G]AAAAGAAATTTGTCT | 11059 |
rs187816716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382219 | AATTTAACAATATAC[C/T]ATAAATATTAAGTTT | 11059 |
rs187828294 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345459 | CTGTCCCTGTGGCTG[C/G]AGTGCAGTGGCGCCT | 11059 |
rs187831428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86448619 | CCTTTGGGAAGTTCT[C/T]CTCACCAGTACCAAT | 11059 |
rs187839419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86411174 | ACACAAGGGAAGGGC[A/G]ATTGAAAGGGATCAT | 11059 |
rs187847549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377555 | CATTTCTGTTCTTAA[A/C]CCTTATCTGATTGGC | 11059 |
rs187982290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86398857 | CACTTTTTAAAAGTA[C/T]ACATTTTAGTCGTTT | 11059 |
rs187983311 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86438960 | GTAGGATCTGATTTT[A/G]TTTTTTTATATAGTG | 11059 |
rs187986372 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86430450 | CACATCTGGCTAATT[A/T]AAAAAAAATTTTTTT | 11059 |
rs187991194 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371536 | GTTTTTACCATTCTA[A/G]TGAATTTAAAAATGA | 11059 |
rs188049387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86377058 | CCAAGTTGTTGCTCC[C/T]TTTATTAGATTACAA | 11059 |
rs188225940 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86378953 | GCTGTTCTTCTGATT[G/T]TTCAAGTAAGGGATG | 11059 |
rs188228045 | snp | C/T | 0.00721081 | 0.0596112 | intron-variant | WWP1 | GRCh38.p7 | 8:86457917 | TTCTGTGCTCATTTC[C/T]CAGGTTATGTTGTGT | 11059 |
rs188230207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419938 | GGGTCCATGCCTTAA[A/G]TGCTGAAGGAAATTA | 11059 |
rs188236177 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86439277 | GAACCCAGGAGGCGG[A/C]GCTTGCAGTGAGCTG | 11059 |
rs188242378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387236 | ACATTCTTCCATTAG[C/T]AGTGGTCCTGTGTAT | 11059 |
rs188248095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405059 | CCTGCTCTGTTGGTA[A/G]CAGCCATTTAACTGA | 11059 |
rs188248165 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86361232 | TGGGCTTGGAGATAA[C/G]AGTTGTAGTGGTAGT | 11059 |
rs188256545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344043 | TGTATTATACAAGCA[A/G]AATGCACCTTTTAAA | 11059 |
rs188276047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419627 | TTCAGACAGTCTGAT[A/G]AGAAAAGTTCTAGAA | 11059 |
rs188284083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86457737 | GGTAAAATAAAGTAC[C/T]AGAGAATCCTTTATG | 11059 |
rs188317237 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86393958 | CATGGGAAATCAGCA[A/G]CCATTGAGAAGACTC | 11059 |
rs188328920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358235 | AAATATTGGTGAGGT[A/G]AGCATGGACTTGAAT | 11059 |
rs188344560 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86423193 | CAAATGTCAGAAAAA[C/G]GGTAATTTTTATTTT | 11059 |
rs188346803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461526 | AGCTGAGGTGGCCAT[A/T]GCTTTGCTCCCTATG | 11059 |
rs188352644 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86399565 | TTCTTCTAAGTTGCC[A/G/T]TTAAGTGATTCTCAT | 11059 |
rs188354535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364202 | GACTTGAATTTCTGT[A/T]AATAAAGTGAATTTT | 11059 |
rs188379406 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86446262 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 11059 |
rs188389130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86346785 | ATTGCCCTTTATAGT[A/G]GTATCCAAGGAACTA | 11059 |
rs188390845 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86365356 | AAGATAGTCGAAGTT[A/G]TTAGATTCTGTGGTT | 11059 |
rs188399584 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86465091 | TTTGAGAGAAAGAAG[G/T]AATTGGGAGAATTGT | 11059 |
rs188399772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86409295 | TTGGAGTACAGTGGC[A/G]TGATCCTGGCTCACT | 11059 |
rs188409853 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86424711 | TCGGCAGGCTGAGGC[A/G]GGAGAATCAGGCAGG | 11059 |
rs188485411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419146 | AGACTAGGGCTGGGC[A/G]CGGTGGCTCCCGTCT | 11059 |
rs188489578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385577 | ATGGAGCAGGTGACT[G/T]TTACCAGAAGTATAT | 11059 |
rs188518499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348023 | ATTAGATCATAAGCT[C/G]TACCATTGAAAAAAA | 11059 |
rs188549553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86369822 | TCCTTCTTTTGCATC[A/G]CAGGCCCCAGTAATT | 11059 |
rs188553459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389465 | TTTCAGAGAGCACCA[G/T]GTTGGGGGTAAGGTT | 11059 |
rs188569548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351607 | GTGCTGGGATTTACA[A/G]GCATGAGCCACCAGG | 11059 |
rs188576533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383381 | CCACTTATCTGCCAA[A/G]TGATCTTCTAGGAAG | 11059 |
rs188610858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444440 | GGAATTCTTGGCACA[C/T]AGAGAGTATTAAAAG | 11059 |
rs188617102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415919 | AACTATGCCTACCGT[A/T]TAGCAGGCACTCAAT | 11059 |
rs188626889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86382869 | TTGCTCTTCTTATTT[C/T]TGTAGAGATTCTCTT | 11059 |
rs188649652 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345705 | CGTAAGCCACCCTGC[C/T]GGGCCTACTGGGAGC | 11059 |
rs188722434 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420866 | AAAAATAGTAAAGGA[C/T]ATTTGTGAAGAAACA | 11059 |
rs188722606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449907 | GGTGTATTTTTTTCT[A/G]TATTCTTCAGCTATT | 11059 |
rs188730769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428190 | TATTTTACTTAGAGC[C/T]AGTCTTGCAGTATGC | 11059 |
rs188738791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86406297 | AGTCCTTGGAGAGTG[A/G]TATTTAAGAAAAATA | 11059 |
rs188738859 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467562 | CATATACTAGATCCA[A/G]TACTATTTAGTTTAT | 11059 |
rs188760587 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86404577 | GAGGAACATGAAGGT[C/T]CCATCATAAATAATT | 11059 |
rs188790079 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445568 | CACCATTGATGGGCA[C/G]CTGGATTTATTCTAG | 11059 |
rs188795244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368440 | AGCCATCCTATAGTC[A/G]TCTGGTCAAAGACCT | 11059 |
rs188872051 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | WWP1 | GRCh38.p7 | 8:86424641 | AACCCCGTCTCCACC[A/G]AAAAAATACGAAAAC | 11059 |
rs188881245 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | WWP1 | GRCh38.p7 | 8:86392028 | CAATAAATTCTTTTG[G/T]CAGCCTTAAGTTTTC | 11059 |
rs188885210 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86408973 | TTGTTGATCTTGTGT[C/T]TGTTCATTTTGCTGA | 11059 |
rs188890601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86373530 | TCTGGATAGAGATTT[C/T]TGTTGTTGTTGAGAC | 11059 |
rs188911469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355809 | TAAGCTTTAGTTGAT[A/G]AGAGAATAGTAACTT | 11059 |
rs188927259 | snp | G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467358 | TGGCTGTTCAGAAAG[G/T]TATTAAGGGCTTAGG | 11059 |
rs188938055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438014 | ACCATGTTAGCCAGG[A/G]TGGTCTCAATCTCCT | 11059 |
rs189054453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86359630 | TCTCAGAGTAAGAGC[A/G]GTTTTGTCTATACCT | 11059 |
rs189055932 | snp | A/G | 0.464297 | 0.136514 | intron-variant | WWP1 | GRCh38.p7 | 8:86424217 | AGACGGGGCGGCGGG[A/G]CAGAGGCGCTCCCCA | 11059 |
rs189056263 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342511 | TTCCTAAGGCAGCAT[C/T]CGAGCGCCCTCGCTG | 11059 |
rs189085844 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468255 | GCTAAGTACATACAG[A/G]AAAACAGTAATTATT | 11059 |
rs189090683 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86428497 | AAGAAACCTAAAATA[C/T]AGAAGCTAGCAGATA | 11059 |
rs189100808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396658 | GAGTACAATAGTGCA[A/G]TCATCACTTGCTGCA | 11059 |
rs189135008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86369123 | GTAGACCTAGTAATA[C/T]GTTGTCATAAAAAAT | 11059 |
rs189156293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455678 | TAAATGAAGAGATAT[A/G]CGATGTTATATTGTT | 11059 |
rs189242358 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86463400 | CAACCTCTGCCTCCC[A/T]AGTTCAAGCGATTCT | 11059 |
rs189282496 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468624 | CAGATTTGACTGAAG[A/G]AGGCAGCTTTCCAGT | 11059 |
rs189313111 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86450859 | TGGGAAGAGAGCTAT[A/T]GTTTCTGCTGGGAGG | 11059 |
rs189381295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450200 | TTTAATGTACCCTTC[C/T]TAGCTTGGCATTCTT | 11059 |
rs189389465 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413108 | TGGGATTACAGGTGT[A/G]AGCCACCATGCCTGG | 11059 |
rs189433553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86349419 | TCTAGCCCAGGTTCA[A/G]GGGTACAAATGTGTG | 11059 |
rs189440675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86454433 | CCTGACTGACATAGA[C/T]TGTCACTAATCCTGG | 11059 |
rs189451077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86356426 | AACTTATCAAATGCA[C/T]GCATATATATATTTA | 11059 |
rs189457179 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86416400 | AGGTCAGTGGAGGGA[G/T]AGATTGGCCAATACT | 11059 |
rs189474426 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86401387 | CAACAAAGGGAGATC[C/T]AGTCTCTACAAAAAT | 11059 |
rs189482758 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367441 | GACTTGAGAAAGACA[G/T]TTTGAAGTAAGCAGG | 11059 |
rs189488432 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86383565 | TGGCCAACATGGTGA[C/G]ACCCTGTGTCTACCA | 11059 |
rs189575512 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86412408 | TTTTCTTTAAAGAGT[A/T]TTCTATATGTGTATT | 11059 |
rs189605392 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86378703 | ATGAGATTAAAGATT[A/G]TTATCTTTGAAAAAT | 11059 |
rs189610662 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343799 | GATAAGTTTAACAAA[A/T]TTTTTTCTGTGTGTG | 11059 |
rs189618965 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381083 | CAAATTATTTCCATT[A/T]TCTCTGACTGTTTTG | 11059 |
rs189625011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421652 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 11059 |
rs189626531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434678 | TCCTTCACTAGTATA[A/T]AAGCTCCACAAAACA | 11059 |
rs189637650 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345305 | TGGTAAAATGCTGGC[C/G]TGGAAAATTTCCATA | 11059 |
rs189637964 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86363543 | ATGGTGGCTCACTCC[C/T]GTAATCCCAGCACTT | 11059 |
rs189639950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406513 | TAAACAGAAAGTTGC[A/G]AAGAAATGTATGGGA | 11059 |
rs189642923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417342 | CTAAGATATTTACCG[G/T]CTGGCTCTTTGTAGA | 11059 |
rs189643113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86455079 | ATGCATAGTCACACC[A/G]CCCTTTTATAGGTTA | 11059 |
rs189701283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433866 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCATTG | 11059 |
rs189721134 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86400453 | GACAGGAATGGAAGG[A/G]AGCCTATTTTTAAAA | 11059 |
rs189732055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374765 | CCCTGGCTGGAGTAC[A/G]GTGGCGCAAACATAC | 11059 |
rs189780900 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86441026 | AAGAATATGTTGAAA[C/G]TTAATTCTTCTGCCT | 11059 |
rs189794336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443323 | AAGTGATCCGCCTGT[C/T]TCGGCCTCCCAAAGT | 11059 |
rs189800835 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86399037 | ATTCTGGCCATTTTC[C/T]ATAAATGGATTCATA | 11059 |
rs189809268 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86459699 | TGCATTATATACAGT[A/T]TGCATACCGTTGTTT | 11059 |
rs189872137 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86360244 | AATAAGTTTCTGGTG[G/T]TTTTTTTTGCTTGGT | 11059 |
rs189892161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464250 | TCTAACTATTTATCT[A/G]TGTGGGGCTATAGAT | 11059 |
rs189909080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435239 | ATCCAGCCATAAATA[C/T]AATGTCCTTCTTTGT | 11059 |
rs189923427 | snp | C/G/T | 8.23765e-05 | 0.00641738 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402095 | AACTCATGCTGCTCG[C/G/T]ATGTAGTTAATGGAG | 11059 |
rs189952204 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86403009 | GAAGGAATGCCTAAG[C/G]AAGATGTCCTCTATA | 11059 |
rs189971028 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384465 | ATACACGTAATTTCC[A/G]GGTTGTGATTAAAAC | 11059 |
rs189979430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367775 | ATCCTGGGGACCAAG[G/T]ACAACTTGATAAAAG | 11059 |
rs189983106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347545 | CCGTGTAGAGGTAAA[C/G]TTGTCAGTTTTTTCC | 11059 |
rs190000007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459297 | TGCCTTGGCCTCCTG[A/T]AGTGCTGGGATTGCA | 11059 |
rs190070693 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86426883 | AGAAGGAGAGGCCGG[A/G]CATGGTGGCTCATGC | 11059 |
rs190163579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86417935 | TATTTCAGTGGGAAG[A/G]CAAACAGTGGCCTTA | 11059 |
rs190219693 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459037 | TCTTTTTTTTTTTTT[C/T]TTTTTTTTTTGAGAC | 11059 |
rs190258807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420611 | AATCACAATAAGTCA[A/G]GGAAGTTAATAAGTA | 11059 |
rs190263028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86388560 | TCTAATCATATTGCC[C/T]TTTTTTCCCTCTAGG | 11059 |
rs190281641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86349659 | TTACTACGCAAATGG[A/G]AATACCTAGCACTCT | 11059 |
rs190373610 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468741 | GCTTTGTTTTGGAGA[A/T]TTCATCAGGGTCTTC | 11059 |
rs190393986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444534 | GGAGATAAGTAACCA[A/G]CAAAAGATCTGAGGT | 11059 |
rs190404650 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408630 | TTAAAGTGTTTTCTT[C/T]ACGCTGGTTGTGCAG | 11059 |
rs190406460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451764 | CTTCTCTGTATGAGG[C/T]GGTGTATGCTGCTTC | 11059 |
rs190424061 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86346891 | ATTGTACTATACCTT[A/C]TGTTAGTATAGCATT | 11059 |
rs190432111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86371823 | AGAAGTCTCAGTTTC[C/T]GTGTAGTCAAAATAT | 11059 |
rs190498779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405635 | CTCCTGGGCTCAAGC[G/T]ATCCTCCTGCCTTAG | 11059 |
rs190502951 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86440128 | GTTCAGACATAAGAA[A/G]GGTACATCTTAGAAA | 11059 |
rs190531887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86369525 | TACAGAGAAAGTTTC[A/G]TGTAGTAAAGTGAAT | 11059 |
rs190538592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86393599 | GCTTAACTTTGTGAG[C/T]TGTTGAACATTGACT | 11059 |
rs190548038 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86410236 | AACACCTTAAATAAC[A/T]TAAGAATGATCTATC | 11059 |
rs190562586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376142 | TTCTACTTTTGCTCT[A/G]TATAAGAAGCTTAGA | 11059 |
rs190569746 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340966 | ATTTGAAACCAAACA[C/G]TCAATAACAAAAGGC | 11059 |
rs190571822 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | WWP1 | GRCh38.p7 | 8:86357956 | TGTCACAATGTTTCT[A/G/T]TGGGAAAATTTGTGT | 11059 |
rs190672515 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86390792 | ACCACTCCCCCATTC[C/T]ACCATAGTAGGAACC | 11059 |
rs190676583 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355066 | GCATGTAGGTCTGTC[C/T]GACTTGAAAACTGTT | 11059 |
rs190718704 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86370009 | CAGCTGAAGAACTAG[A/G]TCAATCCCAATATGG | 11059 |
rs190730685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425947 | TTCATTTACTCACAC[A/G]TTCTATGTGTACCTG | 11059 |
rs190730783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447515 | TCATGATCCACCCGC[C/T]TCAGCCTCCCAAAGT | 11059 |
rs190861833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429416 | TATAATTAACTGGGT[C/G]TGTTACAAGATTATA | 11059 |
rs190871557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413763 | AAAACAGCCCTGTGA[A/T]GAATTTTGTGTGATT | 11059 |
rs190887983 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397010 | TGGGGTTACAGGTGT[A/G]AGCCACCAGGCCTGG | 11059 |
rs190893686 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86352957 | AAATGCCTACTAAAA[A/G]TTAAGCTAGAAGTTA | 11059 |
rs190902037 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361991 | ATATATATATATATA[C/T]ACATATATATACACA | 11059 |
rs190908005 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86379418 | TATTATTCTCTCACA[A/G]TAGAATGGAAGCTTA | 11059 |
rs190954609 | snp | A/G | 0.039522 | 0.134904 | intron-variant | WWP1 | GRCh38.p7 | 8:86389955 | GGGCGGCTGCCAGGC[A/G]GAGGGGCTCCTCACT | 11059 |
rs190959638 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400219 | CACCTGTAATCCCAG[C/T]TACTCAGGAGTCTGA | 11059 |
rs190972613 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86352298 | GGCGCTATCTCGGCT[C/T]ACTGCAACCTCTCCC | 11059 |
rs190985992 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86456341 | TACACCCTGGGAGAA[A/G]CTATTGAGACAAAGA | 11059 |
rs191005528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418352 | TGTATTATTTATTGC[C/T]ATATAATAAATTACC | 11059 |
rs191011868 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86456556 | GTAGTTTCTTGTAAT[A/G]TTAAATGTACATCTA | 11059 |
rs191013628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86394095 | TTGTTATTTTTAGCC[A/G]GTAAGTTTCAGAATA | 11059 |
rs191022046 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437904 | TCCCGGGTTCACACC[A/G]TTCTCCTGCCTTAGC | 11059 |
rs191037053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86357918 | GGGCTTTCACGGCTT[A/G]GTGTTGGTATCCTAC | 11059 |
rs191040148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86418903 | CTAACAGTATCTTCT[A/G]TTGAAGACCTCTCCA | 11059 |
rs191050518 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86385182 | TTGATAGAGATATTA[A/T]GTTTCTGAGGTGTGC | 11059 |
rs191060767 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86403772 | AGTAGACTAAAATAC[A/G]GTTTCCCAAGTACTC | 11059 |
rs191087099 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86452408 | ACTCTAAAATTATAT[A/G]TATTCATACATATAC | 11059 |
rs191184165 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344959 | AGATGATTTTGAATT[C/G]GGAGTGAAACAATTT | 11059 |
rs191244099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410522 | GTAAAAAAATCATAT[A/G]CATTTGTTAAAAATG | 11059 |
rs191265372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86436595 | TAGTACGTAGAATAG[C/T]GCCTTTGCACATAGA | 11059 |
rs191271632 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86377300 | ACGGGGTTTCACCGT[A/G]TTGGCCAGGCTGGTC | 11059 |
rs191314772 | snp | C/G/T | 0.000250426 | 0.0111872 | intron-variant | WWP1 | GRCh38.p7 | 8:86458043 | ATTTGCTTTTATCTT[C/G/T]TTTGAAACAAAGTAC | 11059 |
rs191350473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414341 | CTTACTGTGTAAACT[C/G]TGGTCAAAAAAAGTT | 11059 |
rs191361327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86380302 | ATGTCCAGAATAGGC[A/C]AATTTAAAGAGACAG | 11059 |
rs191463339 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462848 | CAAACTGCTACCTCT[A/C/G]TTCTTCAACACCATA | 11059 |
rs191467115 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86416401 | GGTCAGTGGAGGGAG[A/T]GATTGGCCAATACTA | 11059 |
rs191493990 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86445429 | GAGCTCCCACCTGTA[A/C/T]GTAAGAACATGCAGT | 11059 |
rs191529166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367709 | TTTTGCCAACCCTGC[A/T]TTCTAAATTGCTGAA | 11059 |
rs191560534 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461830 | AAAGACACTTGGTTA[C/T]CAAGAAGCCATACAT | 11059 |
rs191596821 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86429984 | CGGGTGGATCGCTTG[A/C]GCCTAGGAGTTCGAG | 11059 |
rs191610014 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86398070 | GGTACCTTGAGCTGA[A/C]AAGCAAGTTTAGACA | 11059 |
rs191612449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86363072 | AAAAACAAAATTATC[A/G]CAAATTTAGTTACAG | 11059 |
rs191621158 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86404952 | ACAGCATTCCCCTAG[A/C]CTTTTCACCACCTCT | 11059 |
rs191627762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368735 | CAAGCAGTTCTCTGG[A/T]TGTGCCGTTCTTTCT | 11059 |
rs191630774 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386490 | TGTGTGTGTTTGGGT[A/G]GGGGGGCGGGGTGTC | 11059 |
rs191642736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466247 | AATTGAGTATGGCAA[A/G]ATTGAAAAAGTGTCA | 11059 |
rs191642931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348997 | AGCTGATGGCTTAGG[G/T]CTCACAAGAGTACAA | 11059 |
rs191645316 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467792 | CCACTTTTTTGTGTT[C/T]AAAATTTTGGTTTTT | 11059 |
rs191762280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384245 | AAAACTTCAACATAC[C/G]AATTTGGTGGGGGAC | 11059 |
rs191774206 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86419754 | AAATCCAGGATGATA[A/C]ATGAAAACAGATCTA | 11059 |
rs191795197 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86347236 | CGTGGCCCTCCCACC[A/G]TGGCCTTCCAAAGTG | 11059 |
rs191801749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421990 | TCTTGGTGCAGGACA[A/G]CTTATCAAAACTCAC | 11059 |
rs191808509 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86460640 | CTTTCCAAGATTCTC[A/G]TGTATTTCCTTCCAG | 11059 |
rs191832519 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86390024 | CCCAGAAGGGGTGGC[A/G]GTCTGGCAGAGACAC | 11059 |
rs191896277 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WWP1 | GRCh38.p7 | 8:86423372 | CAGAGGACCCTGCGG[C/T]CTTCCACAGTGTTTG | 11059 |
rs191909724 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86407441 | CTGTCCTGTGCATTA[C/T]ATTAATAGAATGTTT | 11059 |
rs191917107 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86370987 | TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA | 11059 |
rs191937098 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86353721 | CTCCTGACCTCAAGT[A/G]ATCCGCCTGCCTTGG | 11059 |
rs192086728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447074 | AGTGAATGCAGTAGG[A/G]AAATGTGATTACCAG | 11059 |
rs192092243 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444068 | GGGGGCATAGGAAAA[C/T]ATGGATAGAAGCAGG | 11059 |
rs192117307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86407119 | TGGGTGTGGTCTTAT[A/G]TCTTGTGGAGATGAG | 11059 |
rs192117877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409576 | TAGAAGTTCTTACAA[C/T]AGGCTGGGCACAGTG | 11059 |
rs192123956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347706 | TACATTGGTGAAATG[C/T]AGATATTTATTTTTT | 11059 |
rs192125899 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | WWP1 | GRCh38.p7 | 8:86375063 | AATATCTGTTTTTAT[A/C]CTACTACACCAGTTC | 11059 |
rs192128359 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449075 | AAACTCTTGGCCTCA[A/G]GTCATCCTCCTTTCC | 11059 |
rs192142014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86370733 | AGTGTAGAATGTTAA[A/G]TCTTGGAGACAGAAC | 11059 |
rs192144637 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467440 | TGAAGACAGGTGCTT[G/T]AACTTGTCAGTTTGT | 11059 |
rs192146704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86411947 | GATTATTGAATGTGT[A/G]CATAAAATGTTTTCA | 11059 |
rs192155026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427324 | GATAGCTGCAGCAAA[C/T]GACCATGGCACATGT | 11059 |
rs192165032 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396173 | GCGCGATCTCAGCTC[A/G]TTGCAACTTCCACCT | 11059 |
rs192171135 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344411 | GCTGTTTACCCCACG[G/T]TGGCTGAAATTTCCT | 11059 |
rs192185640 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86378151 | TACACGTTTACTGTT[C/T]TTGATTTTTCTTTGG | 11059 |
rs192194708 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359787 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11059 |
rs192302685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415712 | CTACTATAGATTAAT[A/T]TTCCCTGCTGTAGAA | 11059 |
rs192305057 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86372373 | CCGTGTTGGCCAGGC[A/G]GGTCTTGAACTCCTG | 11059 |
rs192310456 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86432464 | ATTGCTCCAACAGTT[A/G]TCACCTTTGTGTTGC | 11059 |
rs192311687 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86355078 | GTCCGACTTGAAAAC[G/T]GTTCTCTGCATTACA | 11059 |
rs192318707 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399300 | CCTTCCTTCAGACAT[A/C]ATTGTGGCCTTCCCT | 11059 |
rs192331016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86382784 | TTTATTTAGTTTCCC[A/G]TTGTCTGACACTTAA | 11059 |
rs192350654 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86434195 | CAAAATTTAATTAAA[A/C]GTCATTTATTTGCAC | 11059 |
rs192385859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86408583 | ATTGAGAGATATTTT[A/G]TGTCTGTATTCATTC | 11059 |
rs192418398 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86371586 | TCTCTGATGGGCAGT[A/G]AGATTCAACATTGTT | 11059 |
rs192473952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465616 | CACAGCCAGACCCTG[A/T]CTCCAAATAAATAAT | 11059 |
rs192475522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453271 | GTTGATACCTCCTAT[A/G]AGTGAAATCATACAG | 11059 |
rs192487838 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368168 | CATATACTCTAAGTG[C/T]TAAGTGTTTTACATG | 11059 |
rs192509980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86393266 | GGCTGGAGTGCACTG[A/G]CACGATCTCGGCTCA | 11059 |
rs192562502 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86358534 | TCTCCCAGGCTAGAG[A/T]GCAGTGGTGCCGTCA | 11059 |
rs192609515 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420154 | GGGTCTGCTAGGAGA[A/G]GAGTGAAAGGAATGC | 11059 |
rs192611620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439362 | AAAAAAAAAAAGTTT[G/T]TAAAGCTTTTTGTAG | 11059 |
rs192621868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405232 | GTTTTTGGAGATGGG[A/C]TAGGGGTGTGCATAT | 11059 |
rs192651877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377574 | TATCTGATTGGCAGC[A/C]ACATGTAAGAATAAG | 11059 |
rs192674879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359086 | CCAACACAGTCCCCA[A/G]GTGATTCTGCCATGC | 11059 |
rs192684804 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342223 | GCTAAATGCAATTAT[C/T]TACTCTTGCAATGTG | 11059 |
rs192701705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457754 | GAGAATCCTTTATGC[C/T]AAATTGCCACAGTTT | 11059 |
rs192738829 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86454688 | TATAGTGGGAGCCCT[A/G]TATTGAAGTGGAGAT | 11059 |
rs192754002 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86390639 | AGTGAACCGAGATGG[C/T]GGCAGCACAGTCCAG | 11059 |
rs192762256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354249 | TATAATACCTTCTCA[C/T]TGATGTCAGATCTAT | 11059 |
rs192765947 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86454113 | TTCTGTAGGGCACCT[A/G]TGGACACCACAATCC | 11059 |
rs192771793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86416049 | TGGTTAACAAGGTCA[A/G]AAGCCACTGAAAAAT | 11059 |
rs192775958 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86383134 | TTGGCTTAAAACTTT[C/T]TCTTTTTCTTAAAGC | 11059 |
rs192787432 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345716 | CTGCCGGGCCTACTG[C/G]GAGCTTTTTAAAACA | 11059 |
rs192844514 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341673 | ATCTTAAAACGTGAT[C/T]ATGCTGAGGAGTTGT | 11059 |
rs192859176 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368641 | CAATATAAACTATTC[C/T]ATAGGATCCTATGCA | 11059 |
rs192901498 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86439111 | CACTTTGGGAGGCCA[A/G]GGCGGGTGGATCATG | 11059 |
rs192930878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438174 | ATAAGGAAGATAAAA[C/T]ACATATACTGTTCAT | 11059 |
rs192940853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86404635 | AAATCTATGACAATC[A/G]GAAAAATAGTGATAA | 11059 |
rs192951472 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342659 | CGCGGCCACGCGGCG[C/T]GCTCCCGAGGAAGGG | 11059 |
rs192966202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432997 | TCTCCTTTAAACCAA[C/T]TCCAAGGAAGTTCCC | 11059 |
rs192985563 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86400339 | CTTCGTCTCGGGGGG[A/T]AAAAAATAAATAAAT | 11059 |
rs192992557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86364784 | GCACTCTATCCTGGG[C/T]GACAAAAGTGAGACC | 11059 |
rs193005395 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390940 | CATGGTTTTTCATCT[A/C/G]TCTTTTCTGATATAT | 11059 |
rs193016600 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363910 | AAAATGACAAAAGTA[A/G]TGTACGTGAAACACA | 11059 |
rs193063126 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86348517 | GCCACCACGCCTGGC[C/T]GTCTTGACATTTCTT | 11059 |
rs193090527 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86424225 | CGGCGGGGCAGAGGC[A/G]CTCCCCACATCTCAG | 11059 |
rs193127753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86448633 | TTCTCACCAGTACCA[A/G]TGTTCTTGAAAAAAG | 11059 |
rs193133540 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86387618 | CCTAGGTTCAAGCAA[G/T]TCTCCCACCTCAGCC | 11059 |
rs193136877 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86411318 | CATACTTAAATTTTT[A/G]TCATTTACATATTCA | 11059 |
rs193173013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457637 | ACCATATATACATAC[A/G]GTAAAGGATACATGC | 11059 |
rs193175689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419192 | TGGGAGGCCTGGGCA[C/T]GCAGATCACTTGGTC | 11059 |
rs193177143 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86385916 | CAACACAGCCATGCA[C/G]ATGCTCACATGTCCT | 11059 |
rs193216478 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345491 | CTGGGCTCATTGCAA[A/C]CTCCGCCTCCCAGGC | 11059 |
rs193250608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445593 | TTCTAGGTCTTTCCT[A/G]TTGTGAGTAGCGCTG | 11059 |
rs193251531 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408649 | CTGGTTGTGCAGTGG[C/T]TTACGCCTGTAATCC | 11059 |
rs193278361 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467021 | TCAAAGTATGTTTTC[C/T]GTTCTTCCACAGAAA | 11059 |
rs193285550 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86427188 | AAAAAGAGGGAGAAA[A/G]GATAGCCAGATGATA | 11059 |
rs193290203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86369145 | ATAAAAAATATGGCT[A/G]TAGACTTCTAATACT | 11059 |
rs193292942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395310 | ACTCGCCATTGTAAC[A/G]TGAAAGCAGCCATAG | 11059 |
rs199521023 | snp | A/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457997 | GACATTATACAAGAA[A/G]CAGCAAGCAAATCAT | 11059 |
rs199523467 | snp | A/G | 0.00102834 | 0.022652 | intron-variant | WWP1 | GRCh38.p7 | 8:86448106 | CTCTAAGAAATTGTT[A/G]TTTTGCAAATTTTAA | 11059 |
rs199531543 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353992 | CTTGTTTTAAAACTT[C/T]CTTTGTGATTTAATT | 11059 |
rs199590221 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395326 | TGAAAGCAGCCATAG[A/G]GAATATGTAAATGAA | 11059 |
rs199598335 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387345 | GGTAGAAGGGAGTGC[A/C]AAAATAGCCTGTGAA | 11059 |
rs199603825 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86421504 | AATTGGGTTCTTTTT[G/T]GGGGGGGTTCTCCCA | 11059 |
rs199616388 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381085 | AATTATTTCCATTTT[C/G]TCTGACTGTTTTGGT | 11059 |
rs199647151 | in-del | -/GTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422326 | CCAGTTTGTATTTAT[-/GTA]TTATTTATTTATTTA | 11059 |
rs199656588 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358641 | CACACCCAGCTATTG[-/T]TTTTTTTTTAATTTC | 11059 |
rs199665139 | in-del | -/AG | 0.00953873 | 0.0683987 | intron-variant | WWP1 | GRCh38.p7 | 8:86462412 | GGAAATGAATATGAT[-/AG]GTGTGATTGGAACTT | 11059 |
rs199667539 | snp | A/G | 0.000587391 | 0.0171275 | intron-variant | WWP1 | GRCh38.p7 | 8:86430648 | TATTTCTACTTTCAT[A/G]TTAAAACACTGTTAT | 11059 |
rs199689721 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385043 | AAAAAAAAAAGTAAA[G/T]AACTGCCAAGAACAA | 11059 |
rs199745953 | snp | G/T | 0.000213131 | 0.0103209 | intron-variant | WWP1 | GRCh38.p7 | 8:86452515 | TTTAAGTATTTTACT[G/T]CACATATAAATTACC | 11059 |
rs199755621 | snp | A/G | 0.00103418 | 0.0227161 | intron-variant | WWP1 | GRCh38.p7 | 8:86380713 | ACTCACTAGTGAATT[A/G]TTTGTCTGTTAGTTT | 11059 |
rs199783719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398338 | AGAATATTCTTCTTT[C/G]TAGTGGAAAGAGTGA | 11059 |
rs199822258 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395414 | TTTTTGAGGAGATAT[A/T]TTTTAAGAGAGAATG | 11059 |
rs199830853 | in-del | -/TATATATGTATAT | 0.039522 | 0.134904 | intron-variant | WWP1 | GRCh38.p7 | 8:86431021 | ATATATTATAAGGGA[-/TATATATGTATAT]TATATATGTATATAT | 11059 |
rs199840435 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466556 | TTTTTTTTTTTTAAA[-/T]TTGTCTTTATCCATA | 11059 |
rs199846033 | snp | A/G | 0.00199806 | 0.0315442 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381620 | GCTCTGTTGATACAC[A/G]ATAGAAAATGTAAGT | 11059 |
rs199847266 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381078 | TAAACCAAATTATTT[A/C]CATTTTCTCTGACTG | 11059 |
rs199851304 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344762 | CTAGCAGAGAGGTAT[G/T]TCTAAGAGAGCACAG | 11059 |
rs199872299 | in-del | -/ACAT | 0.105924 | 0.204309 | intron-variant | WWP1 | GRCh38.p7 | 8:86362086 | TACACATATATACAC[-/ACAT]ATATATATACACTAG | 11059 |
rs199876369 | snp | A/G | 0.000367831 | 0.0135565 | intron-variant | WWP1 | GRCh38.p7 | 8:86430787 | ATCTATAAGGGAGAT[A/G]TATATCTCTCCATAT | 11059 |
rs199877389 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86410660 | TAGGAAATTCTGATC[-/T]TTTTTTTTGGGTCTT | 11059 |
rs199881497 | snp | A/G | 5.02391e-05 | 0.00501169 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411828 | GGGTGTATGGATCCT[A/G]TACGGCAGCAGTCTG | 11059 |
rs199897378 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412885 | CCAGGCTAGAGTGCA[A/G]TGGCACGATCTTGGC | 11059 |
rs199916257 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | WWP1 | GRCh38.p7 | 8:86424380 | CGGCCAGGCAGAGAC[G/T]CTCCTCACTTCCCAG | 11059 |
rs199919126 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348914 | GGGCAGGTTTTGCTG[A/G]TGATCACTCTAATGG | 11059 |
rs199956267 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394956 | AAAAAAAAAAAAAAA[C/T]CCAGGAGATGAGGGG | 11059 |
rs199963155 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349030 | AGAAGCAACCAGATC[-/T]TTTTTTTTTGAGAGG | 11059 |
rs199985016 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402159 | CCAGACCCAAAAATA[C/T]ACCAGCTCCAAAACC | 11059 |
rs199989601 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348407 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 11059 |
rs200016346 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444342 | TTAAGTTTGAAGTAG[A/G]CATCCACATGGAGAT | 11059 |
rs200017492 | in-del | -/AT | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86433303 | TTATGCTTTTAAAAC[-/AT]GTGCCTGCTAATGAC | 11059 |
rs200024940 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442849 | AGGCTTTTAAAAAAA[A/T]AAAAAAGGATAAGCA | 11059 |
rs200037897 | in-del | -/CAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416445 | TAACTCTGGGATTGT[-/CAG]AGTTATGACAAGGCA | 11059 |
rs200039723 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396566 | CACATGGTTTAAACA[-/T]TTTTTTTTTTTTTTG | 11059 |
rs200063533 | snp | A/C | 0.000100152 | 0.00707573 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411819 | CAGCCAGATGGGTGT[A/C]TGGATCCTGTACGGC | 11059 |
rs200102691 | in-del | -/TTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445974 | TTCTTTTCTTTTCTT[-/TTC]TTTTTTTTTTTTTTT | 11059 |
rs200149548 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442745 | TCCAGACCATCTTTC[A/G]TACTTCTGTTTCATT | 11059 |
rs200170387 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423064 | TTGAAGGTTTCTTCA[-/T]TTTTTTTTTTTTTTT | 11059 |
rs200193279 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | WWP1 | GRCh38.p7 | 8:86380345 | TGGCTGCCTAGGGAT[-/G]GGGGTGGGGAGAGGG | 11059 |
rs200199791 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362008 | CATATATATACACAC[-/AT]ATATATATACACATA | 11059 |
rs200219357 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381082 | CCAAATTATTTCCAT[A/T]TTCTCTGACTGTTTT | 11059 |
rs200228718 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368358 | TCCTGGTTAGGGAAC[C/T]ATCATCCACTCAGAC | 11059 |
rs200237769 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86410719 | CTTTTTTTTTTTTTT[A/G]CTGTATCTGGAATGA | 11059 |
rs200239869 | in-del | -/CCGAAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400095 | CAGTACTTTGGGAGG[-/CCGAAG]CGGGCAGATCATGAG | 11059 |
rs200248439 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468344 | ATTCATAGTAAAGAC[A/G]AAAGAAAGGCAGAGA | 11059 |
rs200287759 | in-del | -/T | 0.0836354 | 0.186609 | intron-variant | WWP1 | GRCh38.p7 | 8:86386627 | ACTTGCCCAAAATTC[-/T]TTTTTGGAATGGAGT | 11059 |
rs200296477 | snp | A/G | 0.499999 | 0.000599041 | intron-variant | WWP1 | GRCh38.p7 | 8:86432562 | AAGCAAAAAAAAAAA[A/G]AAATTACAACTCTTC | 11059 |
rs200323999 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WWP1 | GRCh38.p7 | 8:86356901 | AGGTTGTTTCCACAA[C/T]TGTAAGCATAAATTA | 11059 |
rs200329390 | snp | C/T | 2.2066e-05 | 0.00332153 | intron-variant | WWP1 | GRCh38.p7 | 8:86381677 | TAAGTTTATTTTAGA[C/T]ACTTTGAACATATCC | 11059 |
rs200341450 | in-del | -/TATT | 0.451856 | 0.147493 | intron-variant | WWP1 | GRCh38.p7 | 8:86431162 | ATATTATAGAATATA[-/TATT]ATATTCTACATAATT | 11059 |
rs200390732 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433249 | TTTTTTTTTTTTTTT[A/C]TTAACTACATTCATT | 11059 |
rs200418398 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438825 | ACGGTAACCATTATT[A/G]TTATTACTACTCTTG | 11059 |
rs200431225 | snp | A/C/G | 9.91857e-05 | 0.00704159 | intron-variant | WWP1 | GRCh38.p7 | 8:86457883 | TTATTCTCTTCACTA[A/C/G]ATCTTTATTGTGGCC | 11059 |
rs200435540 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405327 | CTGAAACCAAAAGGA[-/TT]TTTTTTTTTTTTTTT | 11059 |
rs200438463 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395084 | GGGAGCTGAGCTTGA[A/T]CTCCTCTAGTCTACA | 11059 |
rs200465594 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414884 | CATTCTGAATCCCCC[-/A]CCCCATCCCCCCACC | 11059 |
rs200553123 | snp | A/G | 6.64121e-05 | 0.00576209 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466931 | AGCTCTTGCATTTAA[A/G]TACCCCAGCCAAGAA | 11059 |
rs200585765 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442688 | TGAGTATGCGGGCAA[A/G]AACAACTATTGTCTG | 11059 |
rs200611145 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427393 | CCCAGAACTTAAAGT[-/A]AAATTAAAAAAAAAA | 11059 |
rs200614763 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446515 | AATTTTTGTTTTTGT[A/T]GGACTTAGCCAGAAA | 11059 |
rs200667503 | snp | C/T | 9.89691e-05 | 0.00703383 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398414 | AAACTGGTGAATTGA[C/T]AGTTGTGCTTGATGG | 11059 |
rs200669920 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449021 | AATTTTTTTTTTTTT[-/G]TAAAGATAGGGTCTC | 11059 |
rs200676320 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86417169 | GTGGACCAGGAACTC[-/TG]TGTTCTGAGAATGTT | 11059 |
rs200680953 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460848 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 11059 |
rs200692115 | snp | A/C | 6.63053e-05 | 0.00575745 | intron-variant | WWP1 | GRCh38.p7 | 8:86374026 | TTCCCCTTTTTTAAA[A/C]TAGGTTTTAGCTGAA | 11059 |
rs200712043 | snp | A/G | 0.00199806 | 0.0315443 | intron-variant | WWP1 | GRCh38.p7 | 8:86461768 | TGTCTTATTTTCTTG[A/G]TGTAGGAAGTAATGG | 11059 |
rs200744944 | snp | A/G | 0.000731759 | 0.019114 | intron-variant | WWP1 | GRCh38.p7 | 8:86430776 | TTTTGCTAATGATCT[A/G]TAAGGGAGATATATA | 11059 |
rs200745201 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381086 | ATTATTTCCATTTTC[A/T]CTGACTGTTTTGGTA | 11059 |
rs200829163 | snp | C/T | 0.00103268 | 0.0226997 | intron-variant | WWP1 | GRCh38.p7 | 8:86380715 | TCACTAGTGAATTAT[C/T]TGTCTGTTAGTTTCT | 11059 |
rs200843439 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388257 | GTCTGTTTTTTTTTT[-/T]CCTTTTTTCTTTTTT | 11059 |
rs200847228 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395490 | CATACTGTCCCAAAC[A/G]AGAGAGCAAAGAGAA | 11059 |
rs200858774 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86402295 | CCTTTTTGTGTAGTC[-/T]TTTTTTTTGAGACGG | 11059 |
rs200859457 | snp | C/T | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402115 | AGTTAATGGAGACAA[C/T]ACACCTTCATCTCCG | 11059 |
rs200860048 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | WWP1 | GRCh38.p7 | 8:86361829 | CTGTCTGCACACCCC[-/T]TTCTGTCAATGAACT | 11059 |
rs200861665 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412698 | TGTTAGTGTACGTTG[-/T]GTTTTTTTTTTGGAA | 11059 |
rs200863041 | in-del | -/A | 0.0334418 | 0.12491 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468433 | CAAGCCTAAAGAATT[-/A]AAAAAAAAAATTCTA | 11059 |
rs200869416 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392775 | ATCAACACAAACTCA[G/T]ATATTTTGAAGTCAA | 11059 |
rs200895342 | snp | G/T | 0.000699033 | 0.0186823 | intron-variant | WWP1 | GRCh38.p7 | 8:86430758 | CAGGCTGGGGTAAGC[G/T]GTTTTTGCTAATGAT | 11059 |
rs200965759 | in-del | -/TTTTTT | 0.188 | 0.24219 | intron-variant | WWP1 | GRCh38.p7 | 8:86423064 | TTGAAGGTTTCTTCA[-/TTTTTT]TTTTTTTTTTGGAAA | 11059 |
rs201035516 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381084 | AAATTATTTCCATTT[A/T]CTCTGACTGTTTTGG | 11059 |
rs201066229 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362063 | ACACATATATACACA[C/T]ATATATATACACATA | 11059 |
rs201072917 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408221 | TGTTTTTTGTGGCTT[A/C]ACTTCTCATTTCTTT | 11059 |
rs201087938 | snp | A/G | 8.26822e-05 | 0.00642917 | intron-variant | WWP1 | GRCh38.p7 | 8:86398665 | TATTTGAATATGGGT[A/G]GCGACATGATGTGGA | 11059 |
rs201096113 | snp | C/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411722 | TACCAGTGCAGAATT[C/G]GAATCTGAAGCTAGA | 11059 |
rs201127505 | snp | C/T | 3.17183e-05 | 0.00398223 | intron-variant | WWP1 | GRCh38.p7 | 8:86442599 | ATGCTAAAAAATAAC[C/T]TTGACTTATTTTCTT | 11059 |
rs201150004 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414890 | TGAATCCCCCCCCCA[-/T]CCCCCCACCCCCGCC | 11059 |
rs201183675 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | WWP1 | GRCh38.p7 | 8:86460240 | GGTGTTTCATGGGAG[-/A]AAAATACCACAAACT | 11059 |
rs201187430 | in-del | -/TG | 0.0103295 | 0.0711199 | intron-variant | WWP1 | GRCh38.p7 | 8:86380466 | ATGGTTGTGCCACTC[-/TG]AATATAGTGAAACCA | 11059 |
rs201195308 | in-del | -/TGTATGTA/TGTATGTATGTA | 0.264906 | 0.249555 | intron-variant | WWP1 | GRCh38.p7 | 8:86422317 | TCAGAAGTACCAGTT[-/TGTATGTA/TGTATGTATGTA]TGTATTTATTTATTT | 11059 |
rs201195618 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414247 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTGTATGT | 11059 |
rs201240268 | in-del | -/TTT | 0.458084 | 0.138567 | intron-variant | WWP1 | GRCh38.p7 | 8:86405327 | CTGAAACCAAAAGGA[-/TTT]TTTTTTTTTTTTTTT | 11059 |
rs201277837 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448543 | CTTATTAAGCTTAAT[C/T]TCTAGAACACTTCAG | 11059 |
rs201291864 | snp | A/G | 2.19561e-05 | 0.00331324 | intron-variant | WWP1 | GRCh38.p7 | 8:86448100 | ATTGTTCTCTAAGAA[A/G]TTGTTATTTTGCAAA | 11059 |
rs201301754 | in-del | -/AT | 0.480064 | 0.0978296 | intron-variant | WWP1 | GRCh38.p7 | 8:86362063 | CACATATATACACAC[-/AT]ATATATATACACATA | 11059 |
rs201313316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86443183 | ACTCAAACGATCCTC[C/T]CACCTCAGCCTCCCA | 11059 |
rs201328093 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430450 | CACATCTGGCTAATT[-/A]AAAAAAAATTTTTTT | 11059 |
rs201389877 | in-del | -/AGAAAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364830 | GAAAGAAAGAAAGAA[-/AGAAAG]AGAGAGAGAGAGAGA | 11059 |
rs201400948 | snp | A/T | 1.65029e-05 | 0.00287248 | intron-variant | WWP1 | GRCh38.p7 | 8:86435543 | GTACTATAGTGGTAA[A/T]TAAATCTTATACTCA | 11059 |
rs201423896 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86407890 | AACCATTAATAATAC[-/A]TTGTTATTAACTAAA | 11059 |
rs201436587 | snp | C/T | 9.88761e-05 | 0.00703052 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461244 | GAAAGAGACAGACAA[C/T]GAAGTAAGAATGCGA | 11059 |
rs201441962 | in-del | -/T | 0.0463947 | 0.145069 | intron-variant | WWP1 | GRCh38.p7 | 8:86397444 | CACCTCAAATACTTA[-/T]TTTTTTTTGTGATGA | 11059 |
rs201487600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427611 | TTTCTTATATTGAGA[A/G]ATTATTGTTTATTAT | 11059 |
rs201497668 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425595 | AAGGAAAGAAAGGTA[A/G]TATTTAGGACAGTTT | 11059 |
rs201517326 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381077 | ATAAACCAAATTATT[G/T]CCATTTTCTCTGACT | 11059 |
rs201523715 | in-del | -/TGGAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412709 | CGTTGGTTTTTTTTT[-/TGGAA]TTGTTTTTTTTTTTC | 11059 |
rs201545639 | in-del | -/GTGA | 0.000555434 | 0.0166556 | intron-variant | WWP1 | GRCh38.p7 | 8:86438548 | GAACTTGTACTGCAT[-/GTGA]GTATTTAATATTCAT | 11059 |
rs201546677 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459515 | TCTTTGAAAAGGCAG[A/G]GAAAAAACTGGAAAC | 11059 |
rs201550416 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353492 | TTGAGGAGCCTATTG[-/T]TTTTTTTTTTCTTCT | 11059 |
rs201567236 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390258 | CCAGACGACGGGCGG[C/T]CAGGCAGAGACGCTC | 11059 |
rs201572069 | snp | C/T | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402196 | ATCTGAGCCTGCCGA[C/T]GACACTGGTAAGCAA | 11059 |
rs201617981 | snp | A/G | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430714 | TTCAATGTTAGCTGC[A/G]GAAAATGACCCTTAT | 11059 |
rs201619828 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452264 | CTAGGATTTGGCTAT[A/C]TTACTAAATAGTGAA | 11059 |
rs201652395 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402512 | CAACTGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 11059 |
rs201654619 | snp | C/T | 4.96151e-05 | 0.00498047 | intron-variant | WWP1 | GRCh38.p7 | 8:86381496 | TTGTTAATAATTTTA[C/T]CCTTCCAGAAATGTT | 11059 |
rs201662084 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | WWP1 | GRCh38.p7 | 8:86464069 | TGTCTCAAAAAAAAC[-/A]AAAAAAAAGATCAAA | 11059 |
rs201685414 | in-del | -/TTTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445977 | TTTCTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 11059 |
rs201713935 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376323 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 11059 |
rs201729551 | snp | A/G | 0.00199798 | 0.0315436 | intron-variant | WWP1 | GRCh38.p7 | 8:86380681 | TTAGTGTGCAGTACT[A/G]CTTTTTGGCAACACA | 11059 |
rs201766606 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448193 | GGTTTCTCTTTACCA[C/T]TCTACAAGCGTATGT | 11059 |
rs201830684 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348401 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCTC | 11059 |
rs201830760 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435521 | TCACTTCCGTTATTT[A/G]TGCCAGGTACTATAG | 11059 |
rs201858843 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388894 | TATTCCCATTTGCTA[G/T]CAGCCAGTAGACTTC | 11059 |
rs201863324 | snp | A/C | 0.000115389 | 0.0075948 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431632 | TACAGAATGAAGAAC[A/C]CCTGCCAGAAGGCTG | 11059 |
rs201869888 | snp | A/G | 0.000168859 | 0.009187 | intron-variant | WWP1 | GRCh38.p7 | 8:86380892 | TGTAAAGGACGGAAA[A/G]TCTTCACAAGAAAGT | 11059 |
rs201895119 | in-del | -/TTTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445973 | TTTCTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 11059 |
rs201900700 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437892 | GCAAGCTCCACCTCC[C/T]GGGTTCACACCATTC | 11059 |
rs201901338 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86356821 | TAATCTATTTTAATA[-/T]TTTTTTAAAGGTTCT | 11059 |
rs201904767 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363815 | AAAAAAAAAAAAAAA[C/T]AAATTTGTCTGTGGT | 11059 |
rs201919584 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427396 | GAACTTAAAGTAAAA[-/T]TTAAAAAAAAAAGAA | 11059 |
rs201937444 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442842 | TTAGAGAAGGCTTTT[A/T]AAAAAAAAAAAAAGG | 11059 |
rs201951609 | snp | A/G/T | 3.30111e-05 | 0.00406259 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374071 | CACTGCTTCACCAAG[A/G/T]TCTGATACTAGTAAT | 11059 |
rs201960797 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WWP1 | GRCh38.p7 | 8:86395496 | GTCCCAAACAAGAGA[C/T]CAAAGAGAAAAGTCA | 11059 |
rs201996526 | snp | A/C | 0.000324678 | 0.0127371 | intron-variant | WWP1 | GRCh38.p7 | 8:86401992 | AATTATACTTAAATG[A/C]TTGAAATAAGGCATT | 11059 |
rs201996950 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365698 | CGGGTCACAGTGGTT[-/G]ATGCCTGTAATCCCA | 11059 |
rs202016012 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432550 | GATATAAAAAAAAAG[A/C]AAAAAAAAAAAGAAA | 11059 |
rs202068395 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86421503 | AATTGGGTTCTTTTT[-/G]TGGGGGGGTTCTCCC | 11059 |
rs202107014 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428699 | GCCTAGTTTCCATAG[C/T]GTTTCCTGCTGCCTT | 11059 |
rs202218609 | snp | A/G | 3.30115e-05 | 0.00406259 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435654 | GCACTACCTAGTCAT[A/G]TAAAGATCAATGTGT | 11059 |
rs202221520 | snp | G/T | 0.000119477 | 0.00772816 | intron-variant | WWP1 | GRCh38.p7 | 8:86425204 | GTCTCTTACTGTTAT[G/T]TTTGTATTTTTATTA | 11059 |
rs202221570 | in-del | -/TA | 0.0138799 | 0.0821421 | intron-variant | WWP1 | GRCh38.p7 | 8:86384977 | GCAGTGAGCCAAGAT[-/TA]TATACCACTGCATTC | 11059 |
rs267602027 | snp | C/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425279 | TGGATCATAATACTC[C/G]AACTACCACATGGGA | 11059 |
rs367585293 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346817 | TTACTAATACTTAAT[A/G]GAGGAAAAATGATAA | 11059 |
rs367645058 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415384 | TACAATTGACCCTTT[A/G]TTGTGCTTGCCTTAT | 11059 |
rs367656719 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369323 | TTGTTGAAATTGATA[A/G]TTTTATTTGCTGTAT | 11059 |
rs367680509 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441577 | TCTCTTTAAAACACT[C/T]GACCTGCAATCCTGC | 11059 |
rs367681300 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86412264 | CTCTTCTTTTCCTCA[-/G]CTAATATTGAGTGCT | 11059 |
rs367686497 | snp | C/T | 4.54091e-05 | 0.00476471 | intron-variant | WWP1 | GRCh38.p7 | 8:86442616 | TGACTTATTTTCTTA[C/T]AGAGAATGGTTTTTC | 11059 |
rs367691799 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384458 | CAAGAGTATACACGT[A/G]ATTTCCGGGTTGTGA | 11059 |
rs367708970 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394480 | CTCTGCTCTGCTAGA[G/T]ACTTCATTTCATTTG | 11059 |
rs367717181 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351525 | TTTTTTTTTTTAGTA[A/G]AGATGTTGCCCAGGC | 11059 |
rs367767843 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383558 | ACCAGCCTGGCCAAC[A/G]TGGTGAGACCCTGTG | 11059 |
rs367874866 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461910 | TTGTTTTGTTTTTTT[A/T]AAAATATGTAAGATC | 11059 |
rs367877952 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462515 | AGGCTAATTAAAGAA[C/T]TGAGATGTCAAAGAA | 11059 |
rs367902938 | snp | G/T | 1.69513e-05 | 0.00291125 | intron-variant | WWP1 | GRCh38.p7 | 8:86398333 | AAATTAGAATATTCT[G/T]CTTTCTAGTGGAAAG | 11059 |
rs367922814 | in-del | -/CA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406426 | CAGTATGGTGAGTTT[-/CA]GACAGAAGTACATGA | 11059 |
rs368011967 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86414428 | ATATTTTAGGTTGAC[A/C/G]TAAGATGGGTCTTGA | 11059 |
rs368074595 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398594 | ACAGGAAAATGGTGA[C/T]GCCTTACATGAAAAT | 11059 |
rs368078196 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438091 | AGGCCTGAGGCACCA[C/T]ACCCGGCCTGTATAC | 11059 |
rs368091024 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86390477 | GCTGGCAGATCACTC[A/G]CGGTCAGGAGCTGGA | 11059 |
rs368102126 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359400 | GGTGCCATTACTCAG[C/G]TGGGCCCAAGTTTCT | 11059 |
rs368158108 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364859 | AGAGAGAGAGAGAGA[A/G]AGAAGAAAGAGAGAA | 11059 |
rs368174129 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394459 | ACTGAATTAGTTGGA[C/T]AAGATCTCTGCTCTG | 11059 |
rs368181390 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86372149 | CTGCCTCAGCCTCCC[A/G]TGTAGCTGGGACTAC | 11059 |
rs368245018 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438425 | GATATGTATGTCTTC[A/G]TCTAGTTTGTGAAAG | 11059 |
rs368248479 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86408632 | AAAGTGTTTTCTTCA[C/T]GCTGGTTGTGCAGTG | 11059 |
rs368286337 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359484 | ATTTTGTCTATTCTC[A/G]TTGACCATTGTATTC | 11059 |
rs368311644 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86436643 | TTGATGAACAAATAA[A/G]TGAATGCAGTATTTC | 11059 |
rs368317749 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457321 | TTTTTTTATTTTCAA[A/G]TATATAAGATAGCAT | 11059 |
rs368349859 | snp | A/G/T | 3.29849e-05 | 0.00406098 | intron-variant | WWP1 | GRCh38.p7 | 8:86452701 | CCCTTTTATTATGCT[A/G/T]TTGTAGGGAATGTTA | 11059 |
rs368363888 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413811 | TTTTTCTGAAAACCA[C/T]GAATAAGCATTAAAG | 11059 |
rs368366128 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86385731 | ATGACCAACTTGAAA[-/G]TAGACACTGTCTTAT | 11059 |
rs368379582 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446936 | AACACAAAAGTTTTC[C/T]TCTGGTTGCTTCTGT | 11059 |
rs368381848 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86441594 | ACCTGCAATCCTGCC[-/T]TCTCATGTGGCGTCA | 11059 |
rs368385703 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | WWP1 | GRCh38.p7 | 8:86461762 | AAACTTTGTCTTATT[C/T]TCTTGGTGTAGGAAG | 11059 |
rs368412309 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86400912 | TTTAAAACAATGCTC[A/G]GGCTGCTCTGTGGAG | 11059 |
rs368455285 | in-del | -/TT | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86448834 | TTTCTTTACATTCTC[-/TT]GTTTTAAATTTTTGT | 11059 |
rs368493767 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390314 | TGGGCACAGGCTGCA[A/G]TCTCGGCACTTTGGG | 11059 |
rs368501883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346355 | GTGAACCCGGGAGGC[A/G]GAGCTTGTAGTGAGC | 11059 |
rs368524141 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448014 | ATATAATATTTTAGT[G/T]TTCATGATTTATGCC | 11059 |
rs368565138 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351300 | GACAGTTCTAGCTTC[A/G]TTTTGGCATGGGCAG | 11059 |
rs368572142 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413631 | ATTTTCAGTAGAGCC[A/G]ACTGCACATTCAGAT | 11059 |
rs368639560 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454050 | CCTTCTGGCAAGTCT[C/G]ACTAACCTAGGAAGT | 11059 |
rs368667255 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86364663 | ACAAAGAAATTAACC[A/C]GGCATGGTGGTGCGT | 11059 |
rs368675186 | snp | G/T | 1.82794e-05 | 0.00302314 | intron-variant | WWP1 | GRCh38.p7 | 8:86442828 | TTGTTACAAATGTAT[G/T]AGAGAAGGCTTTTAA | 11059 |
rs368739423 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437036 | GATTGATTTTAGTAA[A/G]TGTACATCTGAATTC | 11059 |
rs368766576 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391705 | GGGGTGGGGGGTTCA[A/G]TGGAGGCTCAGTAGA | 11059 |
rs368889565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86375412 | CCCATTTTCCCACTT[C/T]TCTCCCTTGCCCTGT | 11059 |
rs368903677 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396638 | TCGCTCTATTACTCC[C/T]ACTCGAGTACAATAG | 11059 |
rs368912223 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354367 | TTTGTTTGGCAAATG[C/T]TTGTGTGTGGATAAG | 11059 |
rs368913513 | snp | A/G | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461233 | TTACAGTTTGTGAAA[A/G]AGACAGACAATGAAG | 11059 |
rs368942244 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342247 | CAATGTGTTCGAGGT[C/G]ACCCAGCTAGGTCAA | 11059 |
rs368952361 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452934 | CTTGAAGAGTTGTTG[A/G]AACATTATTAATAAT | 11059 |
rs368952788 | snp | G/T | 3.64983e-05 | 0.00427175 | intron-variant | WWP1 | GRCh38.p7 | 8:86411894 | GTTAAGCTTTTTAAT[G/T]TCTGACTTGCATTTA | 11059 |
rs368955294 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400936 | TGTGGAGAGCAGTTA[A/T]GGGATGACCTGTGTA | 11059 |
rs369024258 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359910 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 11059 |
rs369046585 | in-del | -/GAGT | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86359620 | CTCTTCCAAATCTCA[-/GAGT]AAGAGCGGTTTTGTC | 11059 |
rs369087336 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376304 | CCAGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA | 11059 |
rs369098005 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP1 | GRCh38.p7 | 8:86401989 | TTGAATTATACTTAA[A/G]TGATTGAAATAAGGC | 11059 |
rs369098263 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373832 | CTAATGTTTATTTTT[-/T]ATTTTTGCTTACTAC | 11059 |
rs369105688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86423751 | GGTACACTTCCCAGA[C/T]GGGGTGGCGGCCGGG | 11059 |
rs369105959 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346265 | TTTGGGCTGGGGAGT[A/G]GGGAGGAGAGAGGTG | 11059 |
rs369113098 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466538 | TAAAAAGAAAATGGA[-/T]TTTTTTTTTTTTTTA | 11059 |
rs369127749 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397194 | AAGTTAAGGACTTCA[A/T]CAAAAACGTGAAATG | 11059 |
rs369189733 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409207 | TGCTGATTTTAATTT[A/T]TTCTTTTTCTTTTTC | 11059 |
rs369191482 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455190 | CTTAGTTTGATAAAG[A/G]GAATCATCATCAACA | 11059 |
rs369213021 | snp | C/G | 6.63702e-05 | 0.00576027 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411778 | ATTCTAGAAGTAGTT[C/G]TGCTTTTGAAGCAGC | 11059 |
rs369305792 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360192 | TCTAAACATCTTTTA[C/T]GCTTATGTTTCTCTT | 11059 |
rs369314227 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418250 | ATACTGATTTGCAAA[-/A]CAGTTGAAGGCCCAA | 11059 |
rs369334153 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366831 | TCCTGTTTACTCTTT[C/T]ATTTTATAAATTCAT | 11059 |
rs369344340 | in-del | -/T | 0.0832709 | 0.186283 | intron-variant | WWP1 | GRCh38.p7 | 8:86388207 | TCCTACTTACTTTTA[-/T]ATTTCTCTTAGGTAG | 11059 |
rs369366795 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86427035 | GGGCATGGTGGTCTG[C/T]GCCTGTAATCCCAGC | 11059 |
rs369370516 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387029 | GCCCTAATTCCATCC[A/G]TGAGGACTGCGCCCT | 11059 |
rs369372595 | snp | C/T | 3.30278e-05 | 0.0040636 | intron-variant | WWP1 | GRCh38.p7 | 8:86435604 | ATACTATAACTCAGA[C/T]GATATTATGATATTA | 11059 |
rs369407123 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440484 | CAGACATTGCTTTAC[C/T]GTTTTCTAGCATTGA | 11059 |
rs369467707 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379485 | TGTGTATGACATGAA[A/G]GAGGCTTTTCCCTTC | 11059 |
rs369473652 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341587 | GTACACAGTTCTTTC[A/G]AAAAGCTCAGTTAAA | 11059 |
rs369506786 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459185 | GGATTACGGGTGTGC[A/G]CCACCATGCCCGGCT | 11059 |
rs369508849 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406661 | TCTACCTGTGTGTGT[-/GT]ATGTGTGTGTGTGTG | 11059 |
rs369527723 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390714 | GAGGGAGACGGGAGA[A/G]GGGGAGGGAGAGGGG | 11059 |
rs369531114 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412305 | AAACCTTGCTGATTG[C/G]CTCTATTAAAAATGC | 11059 |
rs369584586 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361047 | ACATAGGCATTTATG[A/G]GTTTGGATTTATTGT | 11059 |
rs369655213 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466774 | TGAAAACATCTGATT[C/T]TGTTTTTGTTTCTGT | 11059 |
rs369658767 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370296 | CAGACATAAAAATAG[A/G]CAGAAATATCTCAGT | 11059 |
rs369704672 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403017 | GCCTAAGGAAGATGT[A/C]CTCTATAATCCTTAG | 11059 |
rs369704830 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466316 | AAGACAAAGAAACAT[A/C]TATATTTGTTAATTG | 11059 |
rs369731154 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426652 | CTGAAAATGTGGACA[A/G]TTCATTTTTATGCCA | 11059 |
rs369735999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360965 | TCCTTTGCAGCATTC[A/G]GGGTAATTAGGTTGA | 11059 |
rs369748307 | snp | A/G | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461272 | CGACTATTGCAGTTC[A/G]TCACTGGAACCTGCC | 11059 |
rs369752631 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429057 | GTGTCATCAAGGACC[C/T]GGGTTCTTTCTGCCC | 11059 |
rs369769440 | in-del | -/CTGTAAGCATAAATTAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356901 | AGGTTGTTTCCACAA[-/CTGTAAGCATAAATTAAA]TTGTTCTCTGATGTT | 11059 |
rs369809571 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370946 | TCTTAGCTCACTGCA[A/C]CCTCTGCCTCCCGGG | 11059 |
rs369833686 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468001 | TATTTTTGTCATAAC[A/G]CTTTTTAATTGTTTT | 11059 |
rs369837007 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392077 | GGGAGTTAGGGTTAT[C/G]CCTAAGAGCCTTGAA | 11059 |
rs369853690 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348032 | TAAGCTCTACCATTG[A/G]AAAAAACCCAAAGAT | 11059 |
rs369863129 | snp | C/T | 1.76207e-05 | 0.00296817 | intron-variant | WWP1 | GRCh38.p7 | 8:86402229 | CTATTTATGACACCT[C/T]GTTTAAAGGAAAAGT | 11059 |
rs369900598 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395985 | GAGAAGCCAAATCAC[C/T]AAATTCCAGACACTT | 11059 |
rs369920628 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366608 | GGTCACATGGAAATG[A/G]AAAATCTAACAGAAT | 11059 |
rs369931003 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409222 | ATTCTTTTTCTTTTT[C/T]TTTCTTTTTTTTTTT | 11059 |
rs369982607 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86391401 | AATTTTTTGGCTCTG[C/T]GGAGATGTGTGGTAT | 11059 |
rs369996949 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427398 | ACTTAAAGTAAAATT[-/A]AAAAAAAAAAGAAAA | 11059 |
rs370036792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86443937 | TGCTGTGTGGGACCT[C/T]TAGGAAATTCACATA | 11059 |
rs370078554 | snp | G/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344399 | ATGGTAATCTTTGCT[G/T]TTTACCCCACGGTGG | 11059 |
rs370100282 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374312 | ATTTATTGAACCTAT[G/T]CTGGATGAAGAGAAG | 11059 |
rs370119015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372312 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTAATTT | 11059 |
rs370125792 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351173 | TATAAAGCAGAAAGC[A/T]TGGTGGCTAGAACGT | 11059 |
rs370133616 | snp | C/T | 0.000115885 | 0.00761113 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431446 | GGTTTACTTTGTGAA[C/T]CATAACACAAAAACA | 11059 |
rs370222426 | snp | C/T | 0.000148899 | 0.00862714 | intron-variant | WWP1 | GRCh38.p7 | 8:86461869 | CAAGAATCCTAAATA[C/T]GAAGGTGAAAGCCAC | 11059 |
rs370232616 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358706 | TAGAGACAAGGTTTT[A/G]CCGTGTTGCCTAGGC | 11059 |
rs370305437 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374593 | GCAAAAAATAAAAAA[C/T]ATTTTAACATCCTGA | 11059 |
rs370306559 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375276 | TATATCACCAAATTG[A/G]TAATTAGTTAAGTTC | 11059 |
rs370312881 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413324 | AGTCTCTCATGTGCC[A/G]GTCACTGTGGCAAAG | 11059 |
rs370313562 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356582 | ACTGATACCATTTAG[G/T]TTTATCTTTTGTTGA | 11059 |
rs370327247 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368612 | AAAGTACTATGCATG[A/G]TATATTTTAAATACA | 11059 |
rs370332000 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372015 | GCCTGGCTAATTTTT[-/G]TATTTTTTTTTTTTT | 11059 |
rs370341847 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347300 | CAATCATTGCTTTTT[A/G]GATGAATATGCTGAG | 11059 |
rs370343383 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367974 | AAACCGTGACTCCCA[A/G]ATGTTTCTTCTCCAT | 11059 |
rs370359814 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457207 | TACCTAAAATAATGT[G/T]CATTTCATACATAAG | 11059 |
rs370360845 | snp | A/C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436547 | ATGTGAGCTCCATGA[A/C/G]AGCAGGGACTATTGG | 11059 |
rs370361941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86456666 | CATGTTAATCATTTT[A/G]TTCATCAATGCTAAA | 11059 |
rs370379822 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377746 | TTTAGACTTTCAACA[A/G]GAAACTGTCAGAAGC | 11059 |
rs370402534 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445221 | GAATCAGGGGTACAT[G/T]TGCAGGTTTGTTAAA | 11059 |
rs370585491 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86371296 | TCTGAGTATTTTTCA[A/C/G]TTTTTTTGTTATTAT | 11059 |
rs370587501 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP1 | GRCh38.p7 | 8:86427825 | TCTATTCGGTAATTA[A/G]CAAATTGTAAGATGT | 11059 |
rs370596048 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392682 | AATTCTCTTTAGCCT[G/T]ATTAACTGAGTGAAT | 11059 |
rs370604192 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439236 | TAGTTCCAGCTACTC[A/G]GGAGGGTAAGGCAGG | 11059 |
rs370613602 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403790 | TTCCCAAGTACTCAC[A/G]GTAGGTAGAATTTTT | 11059 |
rs370620437 | snp | C/T | 1.67335e-05 | 0.00289248 | intron-variant | WWP1 | GRCh38.p7 | 8:86435736 | CAGAATAAAACACCA[C/T]TTGTCTCATTGTATT | 11059 |
rs370655307 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368238 | GACTTTGTTTTTCCT[A/G]TTCTACTGCTACAGG | 11059 |
rs370688123 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393028 | AGTTTTATTATCAAA[C/G]CATTTCTTTGATTAT | 11059 |
rs370688411 | in-del | -/GA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405855 | TTTCTAAATTCCAAA[-/GA]AAGTTATGAATTCTG | 11059 |
rs370725819 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355776 | GGCTAGCTTAACAGC[A/C]CACAAAACCACCTGA | 11059 |
rs370738256 | snp | A/C/G | 3.30192e-05 | 0.00406309 | intron-variant | WWP1 | GRCh38.p7 | 8:86398493 | CAGTAAGCTAACTTT[A/C/G]TATGTTTGTAAAATT | 11059 |
rs370820325 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392347 | GTATATTCAGAACTT[C/T]ACTTTGTGTTTCAAT | 11059 |
rs370844847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86431235 | TATATGTTATATTCT[A/C]TATAATATATATTAT | 11059 |
rs370879519 | snp | G/T | | | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468734 | AAAACCAGCTTTGTT[G/T]TGGAGAATTCATCAG | 11059 |
rs370893563 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382478 | CCAGGGTGGGCAGAT[A/C]ACTTGAGATCAGAAG | 11059 |
rs370902687 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86419344 | AATCGCTTGAACCTG[A/G]GAGACGGAGGTTGCA | 11059 |
rs370915104 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371463 | GCCTACCAGCGGTGT[A/G]TAAGAGCCACCACTG | 11059 |
rs370932199 | snp | C/T | 8.34718e-05 | 0.00645979 | intron-variant | WWP1 | GRCh38.p7 | 8:86425339 | ATAGCACTCTTTATG[C/T]ATTTGTAATTATATT | 11059 |
rs370957714 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368032 | TCTAACTAGCTGTCT[A/G]TTACACCTGGTTGTT | 11059 |
rs370960332 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420250 | CAGAAGGCAGGTGCA[A/G]TCATAGAACAGCTAA | 11059 |
rs370964867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461612 | TTCTTATTGCTGGAT[C/G]TCTGCAACAATTTTC | 11059 |
rs371121779 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467736 | TAATAAATTGATGCA[A/G]TTTCATACTTAGGAA | 11059 |
rs371133724 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369280 | TTTAAGTGTCATACA[A/G]CTTTATTAAATGAAG | 11059 |
rs371156233 | in-del | -/ACTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375662 | GATGTAAAAAAGCTA[-/ACTA]GTCTCCTTTTGCTGG | 11059 |
rs371178533 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345471 | CTGGAGTGCAGTGGC[A/G]CCTTCTGGGCTCATT | 11059 |
rs371181355 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379294 | AGTTCAGACATAACA[C/T]TGAACACTCTTTAAT | 11059 |
rs371224018 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446129 | TGGGACCACAGGCAC[A/G]CACCACCACACTCAG | 11059 |
rs371237610 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398910 | TTACCTTCTCTACTG[G/T]CTGATTTCAGAATAT | 11059 |
rs371245042 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453244 | TACTTTGTTTCTGTG[A/G]GTTTGACTACTGTTG | 11059 |
rs371275452 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400338 | CTTCGTCTCGGGGGG[-/G]AAAAAAATAAATAAA | 11059 |
rs371276495 | snp | C/T | 0.00194835 | 0.0311509 | intron-variant | WWP1 | GRCh38.p7 | 8:86461352 | TGTAATTTCTCTGTA[C/T]GTAATTTTGTGATAA | 11059 |
rs371278529 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404808 | AGGAAGTAGAAGAAC[G/T]GTAATTGACATTCCG | 11059 |
rs371293640 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443969 | GAGTTGAGTAGGGCA[A/G]TGAGTGACCTGATCT | 11059 |
rs371337413 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86355704 | TACTTTTACACACTT[-/A]TCTTTTTACGATTAA | 11059 |
rs371362096 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378654 | AATCACATTATTTAT[A/G]TGTACATTTTGCTAG | 11059 |
rs371369859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360005 | AGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 11059 |
rs371372509 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401334 | GGGGGTCAAGATGGG[A/G]GGATCGCTTGAGGCC | 11059 |
rs371406833 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391040 | TCTTCATCCTTGATG[A/G]TATGTGTTATTACAG | 11059 |
rs371416277 | snp | C/T | 6.83422e-05 | 0.00584521 | intron-variant | WWP1 | GRCh38.p7 | 8:86452543 | ACCTATTTTTAAATA[C/T]CATCTTTATTTTCAG | 11059 |
rs371469392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86415425 | CATCTCTTCATCCAT[C/T]TGATTTTTAGTGCAT | 11059 |
rs371475129 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390367 | GGTGGAGGTTGTAGC[A/G]AGCCGAGATCACGCC | 11059 |
rs371534069 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434810 | GAACCTGACAACACA[A/T]GAGAACATTTTTCAT | 11059 |
rs371549398 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376305 | CAGGCGCGGTGGCTC[A/T]TGCCTGTAATCCCAG | 11059 |
rs371640230 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347872 | GGTATCCCTAATTCA[A/G]AGTTTGAAATGCTCC | 11059 |
rs371650373 | snp | A/G | 0.000214601 | 0.0103564 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381552 | AAGTTTGGAGCCATC[A/G]CACTTTAAAAGCAGA | 11059 |
rs371652309 | snp | G/T | 1.67553e-05 | 0.00289437 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398343 | ATTCTTCTTTCTAGT[G/T]GAAAGAGTGAAAGAA | 11059 |
rs371718215 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461996 | AATACAGCATTCTAT[A/T]ACTGAACACTTTAGC | 11059 |
rs371720678 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409600 | CACAGTGGCTCATGC[C/G]TGTAATCCCAGAACT | 11059 |
rs371738174 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364925 | TTAAAAATACAATTG[A/C]GTAGAAACTCACTTT | 11059 |
rs371753417 | in-del | -/AGGGGGAGGGAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390725 | GAGAGGGGGAGGGAG[-/AGGGGGAGGGAG]GAGGAGCGGGAGGGA | 11059 |
rs371785576 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407987 | TTGAGAAATGCATAT[C/T]GTCATGTACACACCA | 11059 |
rs371795924 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454833 | ACCTTTCTTTTACAT[A/G]TAAGATGACTGAAGC | 11059 |
rs371840483 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413749 | ATAATGCTGAAGAGA[A/G]AACAGCCCTGTGAAG | 11059 |
rs371846088 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458079 | ATATTTTCTAATGAA[A/G]TGGTGGTTTTAAAAA | 11059 |
rs371852452 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344160 | ATGGTTAGTATTTTA[A/G/T]AAAATGGAAAGTGTA | 11059 |
rs371855155 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369624 | ATAAGTAATCTATGC[C/T]TCTTGCCTTTATTCT | 11059 |
rs371863493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390606 | GGCTGAGGCAGGAGA[A/G]TCAGGCAGGGAGGTT | 11059 |
rs371872652 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360011 | CTGAGATTGCGCCAC[C/T]GCACTCCAGCCTGGG | 11059 |
rs371876665 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370147 | AAATATGATTGTTTG[A/G]TTTGAATTTCATAAT | 11059 |
rs371937284 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445605 | CCTATTGTGAGTAGC[A/G]CTGTGGGGAACATAC | 11059 |
rs371941164 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402340 | ACCCAGGCTGGAGTG[C/T]AGTGGTGCGATCTCG | 11059 |
rs371945475 | snp | C/T | 3.38203e-05 | 0.00411206 | intron-variant | WWP1 | GRCh38.p7 | 8:86458063 | AAACAAAGTACTCAA[C/T]ATATTTTCTAATGAA | 11059 |
rs371952096 | in-del | -/AAAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451050 | ACCTCATCTCTACAA[-/AAAT]AAATAAATAAATAAA | 11059 |
rs371953172 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359491 | CTATTCTCATTGACC[A/G]TTGTATTCCCAGTGC | 11059 |
rs371982197 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383698 | GTGAACTGAGATTGC[A/G]CCACTGCACTCCAAG | 11059 |
rs371991228 | in-del | -/TC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459022 | TTTCTTTTTCTTTTT[-/TC]TTTTTTTTTTTTTTT | 11059 |
rs372040186 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415437 | CATCTGATTTTTAGT[A/G]CATTTCAATGAGTTG | 11059 |
rs372062503 | snp | A/C/G | 3.30029e-05 | 0.00406209 | intron-variant | WWP1 | GRCh38.p7 | 8:86452720 | TAGGGAATGTTAGTG[A/C/G]GGGGAGGGACTAATT | 11059 |
rs372073465 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86372785 | TTTTTCCCCTTCGTT[A/G]GTCTTATCAGACATT | 11059 |
rs372090884 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406966 | ACGTGGTGCTTTGAG[A/G]TGGATATACCATAAA | 11059 |
rs372104566 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438465 | CATCTCTTGAGTTAA[A/C]AGCATTGTATAAGAT | 11059 |
rs372117754 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383613 | TGAGTGTGGTGGCAC[A/G]TGCCTGTAATCCCAG | 11059 |
rs372125430 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420732 | TTGTTTTTTGCAATA[A/G]GTCTCACAGACTGTA | 11059 |
rs372130356 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451903 | TTACAGCTGCTTTAT[A/G]TATGTCTCTTCAGAA | 11059 |
rs372162120 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420980 | GTGAAACTTGATCAG[G/T]TTTTTAGGTATTCAT | 11059 |
rs372189504 | snp | C/T | 0.000105377 | 0.00725791 | intron-variant | WWP1 | GRCh38.p7 | 8:86430786 | GATCTATAAGGGAGA[C/T]ATATATCTCTCCATA | 11059 |
rs372195464 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462115 | TATTCCCTGTTTTTT[A/C]TGAAGTTTGTGCCCC | 11059 |
rs372216082 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432909 | CATCACACCCAGCCC[A/G]CAGTTCATTTTTATT | 11059 |
rs372217633 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380278 | ATTATATGATTCCAT[A/C]TATATGAAATGTCCA | 11059 |
rs372231275 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445976 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 11059 |
rs372232786 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465699 | CTATATGTGAAAGAT[A/G]TAAGAGAACAGAAAG | 11059 |
rs372242659 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345738 | TTTAAAACAGTAGAA[A/C]CTTCAGGTTCTTCTG | 11059 |
rs372291084 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422554 | TCTTTGGGATTTTTA[A/G]TAGAGATGGGGTTTC | 11059 |
rs372324292 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455334 | ACCCTAGCCAGTGGC[A/G]AAAGCAGAAATAAGA | 11059 |
rs372347078 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359776 | CAGTCCTCGGCGGGC[G/T]CAGTGGCTCACGCCT | 11059 |
rs372434601 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445486 | CCTCCATCTGCATCT[A/G]TGTTGTTGCAAAGGA | 11059 |
rs372443063 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463841 | CGAGGTGGGAGGATC[A/G]CTTGAGCTCAGGAGT | 11059 |
rs372462719 | snp | A/G | 3.61076e-05 | 0.00424882 | intron-variant | WWP1 | GRCh38.p7 | 8:86411496 | GTAATTGATTGCTTT[A/G]TCATTACTTGATAGA | 11059 |
rs372477125 | snp | C/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436585 | CTGTTCTGCCTAGTA[C/G/T]GTAGAATAGTGCCTT | 11059 |
rs372493959 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467603 | GGAAGGATTCATTGA[A/G]CAGCATAGAAGTTTG | 11059 |
rs372497132 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380560 | TTACAGAAACATTCA[A/G]ATGGCTCTCAAGCAT | 11059 |
rs372512422 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409210 | TGATTTTAATTTATT[C/T]TTTTTCTTTTTCTTT | 11059 |
rs372528445 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86410818 | TTTAATCTGAGTGTT[G/T]TCTTTTTGTCATTAA | 11059 |
rs372649535 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362051 | ACATATATATACACA[C/T]ATATATACACACATA | 11059 |
rs372659125 | snp | A/G | 0.000461893 | 0.0151899 | intron-variant | WWP1 | GRCh38.p7 | 8:86435614 | TCAGATGATATTATG[A/G]TATTATTTTTGTTTT | 11059 |
rs372732624 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341606 | AGCTCAGTTAAAATG[G/T]AAGGGGAGAGAGAAC | 11059 |
rs372758538 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444882 | GTGATGACTAAGTAT[C/T]TTAGTCTGTTTTGTG | 11059 |
rs372776883 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406352 | GGTCATAACTTCTAG[C/T]GTCAAATAACTTTTT | 11059 |
rs372778349 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436543 | TAGAATGTGAGCTCC[A/G]TGAGAGCAGGGACTA | 11059 |
rs372791390 | in-del | -/TAAAG | 0.00993419 | 0.0697739 | intron-variant | WWP1 | GRCh38.p7 | 8:86461946 | TAACTGCTTATTCAT[-/TAAAG]TAGTCAGAATTTCAA | 11059 |
rs372806994 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372093 | CAGTGGCGCGATCTC[A/G]ACTCACTGCAAGCTC | 11059 |
rs372815272 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418284 | TTGTGGAGCGTATGG[A/T]CTAATATATAGGTCT | 11059 |
rs372821973 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449346 | CCAGGCAGTAAACTT[C/T]TTAGGCTTACAGGCA | 11059 |
rs372829672 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86350909 | GAGAATTAGTTAAAT[G/T]AACCTGTTTTGTATA | 11059 |
rs372830528 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347831 | GATATAAATGAGGAT[C/G]TAATTTCCAAAATAT | 11059 |
rs372834946 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427305 | AAAACCTAGATGATG[A/T]GTTGATAGCTGCAGC | 11059 |
rs372879086 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465769 | TTTTTTTCTGACCTT[A/G]TTATCATACTCTACC | 11059 |
rs372889362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378145 | TTAAAATACACGTTT[A/T]CTGTTCTTGATTTTT | 11059 |
rs372903662 | snp | A/G | 0.000329489 | 0.0128311 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402111 | ATGTAGTTAATGGAG[A/G]CAACACACCTTCATC | 11059 |
rs372965218 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377882 | CTTTTTAAAGTAAAA[-/GT]GTCAAATCATATACC | 11059 |
rs372997647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435114 | AGAATTTCCTTCCAC[A/G]TCTCTTCTGTCTGGA | 11059 |
rs373075087 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86460504 | TGTGAGAACTAAATC[C/G]ATGAAAACCAGTGGC | 11059 |
rs373146443 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86445723 | CTCTTAGTTCATTGA[A/G]AAATTTCCAACCTGC | 11059 |
rs373156436 | snp | C/G | 1.67259e-05 | 0.00289183 | intron-variant | WWP1 | GRCh38.p7 | 8:86425344 | ACTCTTTATGCATTT[C/G]TAATTATATTTTATC | 11059 |
rs373157142 | in-del | -/C | 0.00023801 | 0.0109063 | intron-variant | WWP1 | GRCh38.p7 | 8:86440587 | CTTTTTCCTGAAGTT[-/C]AATAATTTCACTGTT | 11059 |
rs373177893 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WWP1 | GRCh38.p7 | 8:86461347 | TTCACTGTAATTTCT[C/G]TGTACGTAATTTTGT | 11059 |
rs373220036 | in-del | -/C | 0.482008 | 0.0931261 | intron-variant | WWP1 | GRCh38.p7 | 8:86423812 | GGCCGGGCAGAGGCG[-/C]CCCCCCCCCACCTCC | 11059 |
rs373252215 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374455 | TTAGCCATTTGTTCA[A/G]TCATTGGGCAAATAT | 11059 |
rs373257572 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355793 | ACAAAACCACCTGAC[A/G]TAAGCTTTAGTTGAT | 11059 |
rs373284446 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353960 | TTTTTCTAGGTTAAA[A/C]ATTTTGGTAATTGTA | 11059 |
rs373311302 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417195 | AATGTTGTCAGCAGC[A/G]GGAACTGGGTACACA | 11059 |
rs373334216 | snp | A/G | 6.60077e-05 | 0.00574452 | intron-variant | WWP1 | GRCh38.p7 | 8:86461747 | TTTAAAGGACCAGAT[A/G]AACTTTGTCTTATTT | 11059 |
rs373344955 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86401911 | AAAATTTTAAAAAAG[A/G]AATAACAAAAAAGAA | 11059 |
rs373364659 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344506 | AAGATGAACCGATTA[A/G]CAATTTCTGCCTTCA | 11059 |
rs373374504 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459010 | GGAGTCATTCTTTTT[C/T]TTTTTCTTTTTTCTT | 11059 |
rs373392396 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430815 | TATATATATATATAT[A/C]TATATATATATATAT | 11059 |
rs373424950 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417411 | TAAAGTGCATTCTAG[A/G]AAATGCACTTTAGAA | 11059 |
rs373429602 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393556 | TAAATAAATTCTGAA[A/G]TTTTTTGTTACATGG | 11059 |
rs373455019 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349652 | ATCTGGCTTACTACG[C/T]AAATGGGAATACCTA | 11059 |
rs373475559 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341756 | GAGCAGGCAGTGGAG[-/AG]GAGCAGGGACATCTA | 11059 |
rs373524632 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467268 | ACCTTGTTAATATTA[C/T]CTAGGGGAAAAAGTG | 11059 |
rs373553709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428419 | AAATGGTGTGATCAT[A/T]GGAGGTAGAAAAGAT | 11059 |
rs373564079 | snp | G/T | 1.66156e-05 | 0.00288228 | intron-variant | WWP1 | GRCh38.p7 | 8:86442789 | CCATGGTGAGTTCCT[G/T]ACTTTATTATTATTT | 11059 |
rs373666777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375667 | AAAAAAGCTAACTAG[C/T]CTCCTTTTGCTGGAC | 11059 |
rs373705326 | snp | C/T | 1.67891e-05 | 0.00289729 | intron-variant | WWP1 | GRCh38.p7 | 8:86435745 | ACACCATTTGTCTCA[C/T]TGTATTCTGTGCATC | 11059 |
rs373736886 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398597 | GGAAAATGGTGATGC[C/T]TTACATGAAAATGGA | 11059 |
rs373738847 | snp | A/G | 0.000103212 | 0.00718298 | intron-variant | WWP1 | GRCh38.p7 | 8:86401973 | TTCTCATGAAATGTT[A/G]TTGAATTATACTTAA | 11059 |
rs373766321 | snp | G/T | 1.66546e-05 | 0.00288566 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411806 | AGCCAAATCAAGACA[G/T]CCAGATGGGTGTATG | 11059 |
rs373779643 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409226 | TTTTTCTTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 11059 |
rs373799586 | in-del | -/TAAAG | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86427387 | ATGTATCCCAGAACT[-/TAAAG]TAAAATTAAAAAAAA | 11059 |
rs373842590 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429353 | GTTTCTACCTCCAAC[-/A]AAAACAGGGTTTTGG | 11059 |
rs373911965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394417 | TTTTTTAAGCACCTA[C/T]CTTCTCTCAGTTGCT | 11059 |
rs373927088 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382783 | ATTTATTTAGTTTCC[C/T]GTTGTCTGACACTTA | 11059 |
rs373964378 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343975 | ATTTTTTTTTTTTAA[C/T]AAGAGTTCATGTTTA | 11059 |
rs373974276 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456233 | TTTTAGAACACAAAA[-/A]GCAATAACCATGAAA | 11059 |
rs373988990 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394216 | AACATGTTTTCAACA[A/G]ATCCATGATTTATAG | 11059 |
rs374006142 | snp | C/G/T | 0.000103884 | 0.00720642 | intron-variant | WWP1 | GRCh38.p7 | 8:86425197 | GTGTGTTGTCTCTTA[C/G/T]TGTTATTTTTGTATT | 11059 |
rs374027324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415143 | AGCACGATTTTGCCT[A/G]AAGAACTTTGCATGT | 11059 |
rs374036882 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349839 | TGATTTACCCGATCT[C/T]GTGAATTGGAACAGA | 11059 |
rs374038412 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369299 | TATTAAATGAAGTGC[A/G]GAGAATAATTGTTGA | 11059 |
rs374047848 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454405 | CGATATATATGAAAA[A/C]CAGGACTCTGAACCT | 11059 |
rs374052706 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430032 | GGCAAAACCTTGTCT[C/T]TACAAAAAATACAAA | 11059 |
rs374068693 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357012 | AAAATAAAATGGTTT[G/T]TATACAAGGATTGCA | 11059 |
rs374156202 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453827 | TATCAAGAATTTTCT[A/G]AAGCTTATTTTCCCA | 11059 |
rs374177049 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383810 | GATACGGATATGCTC[A/G]GGAAAAATAAAATTT | 11059 |
rs374181697 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366059 | GTGCTTCGCAAATGT[A/G]AAGTATTAATGACAT | 11059 |
rs374182968 | snp | C/T | 4.94817e-05 | 0.00497377 | intron-variant | WWP1 | GRCh38.p7 | 8:86461760 | ATAAACTTTGTCTTA[C/T]TTTCTTGGTGTAGGA | 11059 |
rs374189926 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387107 | GTAGTGATTAAGTTT[C/T]AACATACAAATTTTG | 11059 |
rs374207044 | snp | C/G | 1.65353e-05 | 0.00287531 | intron-variant | WWP1 | GRCh38.p7 | 8:86398545 | GAAGTATATAAAAAC[C/G]TAGTTTTTTTCTTTC | 11059 |
rs374294763 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368798 | GACGCAGTTCTCTCA[A/G]AGGTTATCTTCTCTG | 11059 |
rs374308629 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347358 | TTTCCAAAGTATGTG[A/G]CTAGTTAGTGGCCAC | 11059 |
rs374381032 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413362 | AGAAGCTGTTCTTAC[C/T]GTCAAGAACCTCATC | 11059 |
rs374391881 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345490 | TCTGGGCTCATTGCA[A/G]CCTCCGCCTCCCAGG | 11059 |
rs374402851 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456254 | AACCATGAAAGAAAA[A/T]TATGGATACATTGGA | 11059 |
rs374424758 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388618 | GTGTTCTGGTTTTGA[G/T]TGATACTGTTAGTCA | 11059 |
rs374426200 | snp | C/T | 0.000251528 | 0.0112116 | intron-variant | WWP1 | GRCh38.p7 | 8:86435742 | AAAACACCATTTGTC[C/T]CATTGTATTCTGTGC | 11059 |
rs374452710 | in-del | -/TCTCTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430791 | TAAGGGAGATATATA[-/TCTCTC]TCTCTCCATATATAT | 11059 |
rs374483987 | snp | A/C/G | 0.000144593 | 0.00850174 | intron-variant | WWP1 | GRCh38.p7 | 8:86448125 | TGCAAATTTTAAATA[A/C/G]AATTTTTCATTTTTC | 11059 |
rs374486355 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362770 | AATGCTAGACAAGAT[A/C]GAGTGTAGTGTCTTT | 11059 |
rs374495964 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86457395 | AATTTGGATAGCCAG[G/T]TTGGGGGAGATCTAT | 11059 |
rs374517688 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358540 | AGGCTAGAGTGCAGT[A/G]GTGCCGTCACAACTC | 11059 |
rs374559275 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398431 | GTTGTGCTTGATGGA[C/T]TGGTGATTGAGCAAG | 11059 |
rs374577305 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342580 | GAGGCTTTGGGCGGC[C/G]GCGGCGTAGCGCGCG | 11059 |
rs374581903 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381172 | TAATGGCATAAATTT[A/G]TGTATAGTAAAAGTA | 11059 |
rs374642232 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341577 | GTTGTTTTTGGTACA[C/T]AGTTCTTTCAAAAAG | 11059 |
rs374642415 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453025 | TTAGTGGTCTTAACT[C/G]TATTTAGACTTGTTA | 11059 |
rs374653846 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86379363 | AATCTTGCATTTATC[A/C]CATTGTATTTCAGTG | 11059 |
rs374661823 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401642 | GAAACTACTTTCAGA[A/G]CTTTTAAAATAGATT | 11059 |
rs374747317 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419389 | CACCACTGCAGTCCA[C/G]CTTGGGTGACAGAGC | 11059 |
rs374808159 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408449 | TTCCAAAGTGGCTGT[A/G]CTCCTGCATTCCCAC | 11059 |
rs374816849 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390716 | GGGAGACGGGAGAGG[A/G]GGAGGGAGAGGGGGA | 11059 |
rs374831543 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424847 | GGAGGGGGAGGGGAG[-/C]GGGAGGGGGAGGGGG | 11059 |
rs374840958 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384253 | AACATACGAATTTGG[C/T]GGGGGACACAATTCA | 11059 |
rs374889410 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381855 | ATCCACAAGTACCCT[A/G]TTATCAGTGACTATC | 11059 |
rs375025581 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432318 | GGTCTTTTGCAAAGT[C/T]GTACCACCATATCTG | 11059 |
rs375041897 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, missense, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468706 | TGAGGCTACACAGAA[A/C]CCTACAAGAGACAAA | 11059 |
rs375083198 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396214 | AGCAATTCTCCTGCG[A/T]CAGCCTCCTAAGTAG | 11059 |
rs375091817 | snp | A/C/G | 0.000511037 | 0.015977 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461229 | TTCATTACAGTTTGT[A/C/G]AAAGAGACAGACAAT | 11059 |
rs375123726 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396592 | TTTTGCAAAGAATTT[C/T]TTTTTCTTCTTTCTT | 11059 |
rs375155087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86421435 | AGTATATATGGTTAT[C/G]GTGTATAAAAATAAT | 11059 |
rs375161512 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394614 | GTCCTGCTTCTTCCC[A/C]ATCTACAGTGCCTGG | 11059 |
rs375168620 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86441999 | CTTATCACATTTAAA[G/T]ATTTAACCTTTTAAA | 11059 |
rs375183533 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441236 | CTCACAAGACCTGCT[C/G]CATCCTCTTACCTGG | 11059 |
rs375206439 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WWP1 | GRCh38.p7 | 8:86435589 | CTTTATACAATACAT[A/G]TACTATAACTCAGAT | 11059 |
rs375233089 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396482 | TTGTTTGTTTGTTTT[C/T]GATGTAAAGTAGAAA | 11059 |
rs375254942 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439678 | TTTTCTACATTCACT[A/G]AATATATTGTTAACA | 11059 |
rs375259397 | in-del | -/CAGCATTTGAGG | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86413711 | GTTATAGTTTGAGTT[-/CAGCATTTGAGG]CAGCAAGATATATAA | 11059 |
rs375310245 | snp | C/T | 0.000155988 | 0.00883004 | intron-variant | WWP1 | GRCh38.p7 | 8:86398300 | TCTGAAGCATTTTTA[C/T]ATGTGGCAAAAGCTT | 11059 |
rs375320511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86433713 | GTTTGGGAGGCCGAG[A/G]CGGGCAGATCACCTG | 11059 |
rs375328354 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462379 | GTAAACAAAGACCCC[A/G]AAGAAATTGTTTTTC | 11059 |
rs375348600 | snp | A/C/T | 6.59124e-05 | 0.00574042 | synonymous-codon, stop-gained, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461257 | AATGAAGTAAGAATG[A/C/T]GACTATTGCAGTTCG | 11059 |
rs375350554 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378387 | TCTTCATGTGACTCT[C/T]ACTTATTTCTTAAGT | 11059 |
rs375362237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401192 | GTAGTCATGATTTTA[A/G]TGCCTAGTATATGCT | 11059 |
rs375419539 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347598 | ACTGCAGTGGCTATT[A/G]GTAGGTGATATTTAA | 11059 |
rs375423543 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347847 | TAATTTCCAAAATAT[A/G]TATAGATTGGGTATC | 11059 |
rs375454489 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363794 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 11059 |
rs375473240 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401335 | GGGGTCAAGATGGGA[A/G]GATCGCTTGAGGCCA | 11059 |
rs375488060 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375704 | GTTCCACTGTTTGCT[A/G]TTACCAATAGTGCTG | 11059 |
rs375524985 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86446824 | CTTGAGTTGGAGAGA[-/G]GGAGGAGATTTATTT | 11059 |
rs375525652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86383894 | CACACCTAAGAAGTC[A/G]GTAAATTAGTTTGCA | 11059 |
rs375572644 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345869 | AATGTTATTTGCTAT[C/T]ATATTACACAATAAA | 11059 |
rs375579702 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86412914 | GCTCACTGCAACTTC[C/T]GCCTCCCAGGTTCAA | 11059 |
rs375593042 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350698 | CATTAACAGAATGTA[A/G]GTATGATAGCCTTTT | 11059 |
rs375624984 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359021 | AGTAGTGGGAGAAAC[-/AT]GTGGGAAGTCGTTGG | 11059 |
rs375652219 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454588 | CTGAAGATGGACATC[G/T]TGCATCCTCTAAATT | 11059 |
rs375727216 | in-del | -/TTTC | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367382 | TCTATTCTAATTGGA[-/TTTC]TTTCTTTCTTTCTCT | 11059 |
rs375746632 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364576 | TTGGGAGTCTGGGGT[-/T]GGGAGGCTCACTTGA | 11059 |
rs375759074 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390404 | CTCCAGCCTGGGCAA[C/G]ATTGAGCACTGAGTG | 11059 |
rs375802955 | snp | A/T | 1.67444e-05 | 0.00289343 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402200 | GAGCCTGCCGATGAC[A/T]CTGGTAAGCAAGGCT | 11059 |
rs375827618 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404166 | TTTTGGATTAGGGAT[A/G]CTAAACTGGCAAGTA | 11059 |
rs375836975 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360078 | AAAAACAAAAAAAAA[A/C]CACAATCCTCTAAAT | 11059 |
rs375882491 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86434923 | GTCACTGTGAGTCAA[A/T]CCATATTGTAAAACC | 11059 |
rs375898053 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86385038 | CAAAAAAAAAAAAAA[-/G]TAAACAACTGCCAAG | 11059 |
rs375921073 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465771 | TTTTTCTGACCTTGT[C/T]ATCATACTCTACCTT | 11059 |
rs376028240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417934 | GTATTTCAGTGGGAA[A/G]ACAAACAGTGGCCTT | 11059 |
rs376033100 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86355320 | GTTTGGCCTGCCATT[A/G]AGAAGCTCTGTGTTT | 11059 |
rs376034455 | snp | C/T | 4.9525e-05 | 0.00497595 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381551 | CAAGTTTGGAGCCAT[C/T]GCACTTTAAAAGCAG | 11059 |
rs376037022 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86397031 | CCAGGCCTGGCCACA[A/G]AGAAATTTCTGTCCG | 11059 |
rs376058209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86365512 | CTGGTAGATATTGCA[A/G]GTACTCTTCAAATCA | 11059 |
rs376068337 | snp | A/T | 6.60524e-05 | 0.00574646 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452597 | CTCGAGGAGTACAAG[A/T]ACAGACCAAAGCTTT | 11059 |
rs376087118 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425432 | TATATTCAATTTCTT[C/T]ACATTTCCTTATATA | 11059 |
rs376110798 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | WWP1 | GRCh38.p7 | 8:86427605 | TTTCATTTTCTTATA[C/T]TGAGAGATTATTGTT | 11059 |
rs376162346 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382252 | ATGATACTTTTTCTA[C/G]ACTGGGATTTTAAGG | 11059 |
rs376176040 | in-del | -/CTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396601 | GAATTTCTTTTTCTT[-/CTT]TCTTTTTTCAGACAG | 11059 |
rs376190623 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380082 | TAACAGCTTTATGCA[C/T]AATAGCCACAAAGTG | 11059 |
rs376224043 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446558 | GGCTAATATCAAGAG[A/G]GCATTTCCTAGGTTT | 11059 |
rs376231165 | in-del | -/AAGTTG | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86451574 | GACAAATGGGAAGAA[-/AAGTTG]GAGTTGGAGTTGAGG | 11059 |
rs376264905 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446269 | TTACAGGCGTGAGCC[A/G]CTGCGCCCAGCAGCT | 11059 |
rs376274992 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425952 | TTACTCACACATTCT[-/AT]GTGTACCTGGAATAT | 11059 |
rs376275613 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440575 | GCCCACACAGTCCTT[C/T]TTCCTGAAGTTCAAT | 11059 |
rs376287812 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86461068 | CCTGCTTCGGCCTCC[A/C]AAAATGCTGGGATTA | 11059 |
rs376292875 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372109 | ACTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 11059 |
rs376298492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418654 | GAGAAACCCTAATTC[C/T]CTTCCCTGCAGCCAG | 11059 |
rs376300818 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392953 | TTTATATACACAAAC[A/G]TAGCGTATGACAGCA | 11059 |
rs376305041 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367522 | AGTACTGGAAATGTC[A/G]TTTATTATCTACATT | 11059 |
rs376310736 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430817 | TATATATATATATAT[A/G]TATATATATATATAT | 11059 |
rs376343550 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86353317 | GGATCCAAAATCTGA[G/T]CCTGTCATCAGAAGA | 11059 |
rs376371785 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416977 | TCTGGTCACCACCAC[A/G]TTCTGGGGACTCACT | 11059 |
rs376392848 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459023 | TTCTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 11059 |
rs376433419 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452425 | ATTCATACATATACA[C/T]ACACATCACATTTAT | 11059 |
rs376455074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86461590 | AGTTTTCTTCCCAAT[A/G]ATCTAATTCTTATTG | 11059 |
rs376462170 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396879 | GCTGGGATTAGAGGC[A/G]TGAGCCACCGTGTCT | 11059 |
rs376535570 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435653 | TGCACTACCTAGTCA[C/T]GTAAAGATCAATGTG | 11059 |
rs376550150 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389898 | CCCCCACCTCCTGGA[C/T]GGGGCGGCTGCCGGG | 11059 |
rs376565445 | snp | A/G | 5.02046e-05 | 0.00500997 | intron-variant | WWP1 | GRCh38.p7 | 8:86435735 | GCAGAATAAAACACC[A/G]TTTGTCTCATTGTAT | 11059 |
rs376616908 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361963 | CTGAAAATATGCCTA[-/GT]GTGTGTGTGTGTATA | 11059 |
rs376616921 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419856 | AAAAAGCAGGTTTCA[C/T]AATAATCAGAATGGC | 11059 |
rs376711780 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86384210 | CTCTAAAAACGTCAC[A/T]TTTTGAGGTACTGGG | 11059 |
rs376712551 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448878 | TTTCACTCTGTCGCT[C/T]AGGCCGTCGTAGTGG | 11059 |
rs376785234 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409216 | TAATTTATTCTTTTT[C/T]TTTTTCTTTCTTTTT | 11059 |
rs376823750 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372981 | ACCTTTCCTTTCCTA[C/G]TATGTCTTTAAGGCT | 11059 |
rs376899914 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412985 | AGGCACCCGCCACTA[G/T]GCCCAGCTAATTTTT | 11059 |
rs376911353 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366978 | CTTTGGAGTTGCTCT[A/G]TTGAGGGGGGAGACT | 11059 |
rs376915887 | in-del | -/TA | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86425951 | TTTACTCACACATTC[-/TA]TGTGTACCTGGAATA | 11059 |
rs376919343 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370893 | TTTTTTGAGACAGAG[C/T]CTTTCTCTGTTGCCC | 11059 |
rs376965989 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408916 | CTCTGTCTCAAAAAA[A/G]AAAAAATTTTTTTTC | 11059 |
rs376984065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436806 | AACCAAATTATGCTG[A/T]GTACTCAGGCATACA | 11059 |
rs376990767 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411654 | ACTACTGTTGAAGAT[C/T]CTCCAGTTCAAGAAA | 11059 |
rs377000797 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379243 | TTTGGAACGATGAAG[A/G]ATGGAAATGAGTTTT | 11059 |
rs377046219 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86424367 | CCCAGACGATGGGCG[G/T]CCAGGCAGAGACGCT | 11059 |
rs377063263 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388832 | AGCATTTATTATTTT[A/G]ACTTCTGCAGTCTTT | 11059 |
rs377068921 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408446 | TCTTCCAAAGTGGCT[-/G]GTACTCCTGCATTCC | 11059 |
rs377083766 | snp | C/G | 6.69355e-05 | 0.00578475 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411826 | ATGGGTGTATGGATC[C/G]TGTACGGCAGCAGTC | 11059 |
rs377084694 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346792 | TTTATAGTGGTATCC[A/G]AGGAACTAGTTACTA | 11059 |
rs377133105 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362057 | ATATACACACATATA[C/T]ACACACATATATATA | 11059 |
rs377149952 | snp | A/G/T | 6.00667e-05 | 0.00547994 | intron-variant | WWP1 | GRCh38.p7 | 8:86438539 | TTTTGAAAGGAACTT[A/G/T]TACTGCATGTGAGTA | 11059 |
rs377158819 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86370537 | GCTTCTGTAATTGTT[C/T]GTTGGACAAACTCTT | 11059 |
rs377164348 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344205 | GGAGCTACTCAGATT[G/T]AGAATTGTAAAGTAT | 11059 |
rs377203401 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414228 | GAAAGTTTGTTTTTC[-/T]GTGTGTGTGTGTGTG | 11059 |
rs377265181 | snp | G/T | 1.65485e-05 | 0.00287645 | intron-variant | WWP1 | GRCh38.p7 | 8:86461363 | TGTACGTAATTTTGT[G/T]ATAATAATGGCCTTT | 11059 |
rs377275005 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439160 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 11059 |
rs377285409 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371385 | CATTGAAGGGCATAC[A/C]AATGTTTAGCTTTAA | 11059 |
rs377301366 | in-del | -/TTG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394896 | CAAATCTTTGTGGCG[-/TTG]ATGATTTTGCAAAAA | 11059 |
rs377319623 | in-del | -/ATAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430799 | GATATATATCTCTCC[-/ATAT]ATATATATATATATA | 11059 |
rs377374631 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462879 | CCCTTGAGGTTTAAA[-/G]AAAAAAAAAAAAAAG | 11059 |
rs377380818 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468159 | TGCTTTTAATATGCA[C/G]TGTAAATTTCATTAA | 11059 |
rs377387565 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427474 | GGAAAAAAAAGATAT[C/T]AGTGGTAGAATGGGA | 11059 |
rs377387911 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403771 | AAGTAGACTAAAATA[C/T]GGTTTCCCAAGTACT | 11059 |
rs377393271 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WWP1 | GRCh38.p7 | 8:86398491 | ACCAGTAAGCTAACT[C/T]TATATGTTTGTAAAA | 11059 |
rs377399050 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422349 | TTTATTTATTTATTT[-/A]TTTATTTATTTATAT | 11059 |
rs377412554 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394074 | CTCGGCAATAATGAG[C/T]GATTATTGTTATTTT | 11059 |
rs377442053 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456324 | TAAGTGAAAAAGCAA[C/T]CTACACCCTGGGAGA | 11059 |
rs377442089 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399207 | AGTCAGATACTATGG[A/T]TAAATAGGTATCATA | 11059 |
rs377454568 | snp | A/C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376741 | CCATGACAGTATTTA[A/C/T]CATTTTGAGCGTCAG | 11059 |
rs377517002 | snp | C/T | 0.00016841 | 0.00917477 | intron-variant | WWP1 | GRCh38.p7 | 8:86380886 | ACCTTGTGTAAAGGA[C/T]GGAAAATCTTCACAA | 11059 |
rs377524451 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450412 | TTCATCAAAAGATCA[C/T]GCATAAGGCACTGGA | 11059 |
rs377540932 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398212 | TACTTAACTAGTTGT[C/T]AAAGGCATGCAAAGA | 11059 |
rs377556503 | in-del | -/TAT | 0.000577772 | 0.0169868 | intron-variant | WWP1 | GRCh38.p7 | 8:86435607 | CTATAACTCAGATGA[-/TAT]TATGATATTATTTTT | 11059 |
rs377604414 | in-del | -/CAAAAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360068 | ACAAAAAACAAAAAA[-/CAAAAAA]AAAACACAATCCTCT | 11059 |
rs377717874 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370985 | ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 11059 |
rs377738924 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403165 | GTTGGGAATTAAGTT[G/T]AAATCCTGGTCTTTT | 11059 |
rs377741550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86428948 | AGAATGTTATCTTGC[A/G]AGTAATAGAATCTCC | 11059 |
rs377745744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381701 | CATATCCTGAATCCT[A/G]AAAGCAAAAACATAG | 11059 |
rs377747444 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367545 | TCTACATTCAGGACT[G/T]TTTTCTGTTCTTTGC | 11059 |
rs377763782 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443871 | AAAGAGACCAGTATA[A/G]TTGCAGCAGAGGATA | 11059 |
rs377766831 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388349 | AGCCTCCAACTCCTG[A/G]ACTCAAGCGATCCTC | 11059 |
rs386727438 | in-del | ACGTGATTATG/CTCCA | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341666 | GGACCTAATCTTAAA[ACGTGATTATG/CTCCA]CTGAGGAGTTGTAGG | 11059 |
rs386727439 | multinucleotide-polymorphism | CC/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371117 | TTGACCTCAAGTGAT[CC/TT]ACCTTGGGATCCACC | 11059 |
rs386727440 | in-del | C/TGTGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414244 | GTGTGTGTGTGTGTG[C/TGTGT]ATGTGTGTGTATGTA | 11059 |
rs386727441 | multinucleotide-polymorphism | CC/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426995 | GTGAAACCCCCATCT[CC/TT]ACTAAAAATACAAAA | 11059 |
rs397687924 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375569 | TGCTTTGCTTTTTTT[-/T]AACTTTACAGTATTA | 11059 |
rs397708741 | in-del | -/GTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441630 | TGAATCAGAGTTGTT[-/GTT]TCCCCTGTAGATTAG | 11059 |
rs397714831 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396580 | TTTTTTTTTTTTTTT[-/T]GCAAAGAATTTCTTT | 11059 |
rs397743246 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436963 | TGATTTTTTTTTTTT[-/T]GAGTTAATAAATTCT | 11059 |
rs397743675 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412709 | GTTGGTTTTTTTTTT[-/T]GGAATTGTTTTTTTT | 11059 |
rs397774376 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391521 | ATAGGAAAAAAAAAA[-/A]TCCCTCTATTGTTAC | 11059 |
rs397891478 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373085 | TGTTTTTTTTTTTTT[-/T]GTAATTTCCAACATG | 11059 |
rs397891960 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341755 | GGAGCAGGCAGTGGA[-/GA]GGAGCAGGGACATCT | 11059 |
rs397943510 | in-del | -/C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410719 | TTTTTTTTTTTTTTT[-/C/T]CTGTATCTGGAATGA | 11059 |
rs397944017 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402430 | GCTGGGATTACAGGC[-/C]ACCCACCACCACAAC | 11059 |
rs397951102 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368475 | GTATCCTGAGTTTTT[-/T]CTTTCATGGTGCCAA | 11059 |
rs398008612 | in-del | -/T | 0 | 0 | intron-variant | WWP1 | GRCh38.p7 | 8:86433248 | TTTTTTTTTTTTTTT[-/T]GTTAACTACATTCAT | 11059 |
rs398008613 | in-del | -/A | 0 | 0 | intron-variant | WWP1 | GRCh38.p7 | 8:86442855 | TTAAAAAAAAAAAAA[-/A]GGATAAGCATTATAT | 11059 |
rs398067998 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395414 | tttTTGAGGAGATAT[-/AT]TTTAAGAGAGAATGG | 11059 |
rs527247142 | snp | A/G | 0.000380546 | 0.0137887 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452576 | TAATGACAGAATGGC[A/G]TTTTTCTCGAGGAGT | 11059 |
rs527272160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390344 | GAGGCCAAGGCAGGC[A/G]GCTGGGAGGTGGAGG | 11059 |
rs527281336 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361252 | GTAGTGGTAGTGATG[A/G]TAAGAAGTAATTGGC | 11059 |
rs527313800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383433 | GAAATGAAGCCCTCA[C/T]GAATTGTATAAGCTA | 11059 |
rs527319182 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86464360 | TCACTCTTTCCACTA[-/T]TTTTTTTTGGAAGTA | 11059 |
rs527333562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375621 | AGAATATTCTTTTTC[A/G]TCATTGCGCCATATC | 11059 |
rs527340532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424577 | GGAGGCTGAGGCTGG[A/C]AGATCACTCGCCGTT | 11059 |
rs527387089 | in-del | -/G | 0.0138882 | 0.0821658 | intron-variant | WWP1 | GRCh38.p7 | 8:86400333 | CAAGACTTCGTCTCG[-/G]GGGGGAAAAAAATAA | 11059 |
rs527389105 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468000 | TTATTTTTGTCATAA[C/T]ACTTTTTAATTGTTT | 11059 |
rs527409256 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416947 | TACCTTCCTCCCTTG[C/T]TGCCCAAGGCCTGCT | 11059 |
rs527449615 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468568 | ATAAATTTTGCCATG[A/G]CAGAAGTTATTGAAT | 11059 |
rs527464905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418615 | TAGTGAAGATGACAC[C/T]GTAAATGGCAGGACT | 11059 |
rs527475833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411453 | TTAGTCTGGATTAGG[C/G]TCTGAATAAGTGTAG | 11059 |
rs527527954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462318 | GGTAAAGAGCATGAT[A/G]TGGGAGTACGCAGAG | 11059 |
rs527531369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370035 | TATGGTTAAAGAGCT[A/G]TGAAAACCTCTCTGA | 11059 |
rs527568204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454727 | AACGGGAGATCAAGA[A/C]GCATAAGAATAGGAA | 11059 |
rs527628877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404840 | TATCTGGCTGTTGAT[G/T]CTGTGCACTTTGCCT | 11059 |
rs527657028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354796 | GAAAAATATTGAGAG[C/T]TTTTGTGCCTTAGAG | 11059 |
rs527662459 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86397559 | AAAATTCCTTCTAAC[G/T]GAAGCTGTGTATCCT | 11059 |
rs527672269 | in-del | -/TG | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86363179 | GTAGTGGCAGAACAC[-/TG]GGTTTTGTGAGATGG | 11059 |
rs527698966 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86439971 | AGATAAGTAATAATA[A/T]ATGTGGAATTATCAG | 11059 |
rs527726818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347363 | AAAGTATGTGGCTAG[C/T]TAGTGGCCACAATTA | 11059 |
rs527774790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86375745 | CTTCATACAAAAGTC[A/G]TTTCTTATGTCTGCT | 11059 |
rs527778590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432867 | CCTGCTTTGGCCTCC[C/G]AAAGTGCTGGGATTA | 11059 |
rs527786562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440650 | AAGATCTTCCTTAAT[A/G]TCAGGGAAGTTTTCT | 11059 |
rs527791936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384453 | TTGGTCAAGAGTATA[A/C]ACGTAATTTCCGGGT | 11059 |
rs527803219 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341814 | AAGTCTGGGTGTGGA[C/T]GTAGATATAATCTAT | 11059 |
rs527833877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354768 | TTCTCTATATTGTTG[C/T]GGAAGTATGGAAGAA | 11059 |
rs527881578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86385164 | ATTTGAGGGGCAAGG[C/T]TATTGATAGAGATAT | 11059 |
rs527890264 | snp | A/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341629 | GAGAGAACCAGAGGT[A/T]TTAAAATCAAGGGAA | 11059 |
rs527905767 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86425999 | AGATTTCCCTTCCAG[A/C]TTCAATTTAAAGCCC | 11059 |
rs527938239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426608 | TAGACTCTCACATGA[A/G]GCCCTTGTAGGATCT | 11059 |
rs527951776 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386531 | TGCAGGCCCTGTGGT[A/T]TACTCAATTATTTTT | 11059 |
rs527995491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463108 | TGCTTTCTTTTATGG[A/G]ACACTATTTTTACTT | 11059 |
rs528001190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377973 | TTTATGGTCTCATCT[A/G]TCTTCCCATTGATTT | 11059 |
rs528014610 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392952 | ATTTATATACACAAA[C/T]GTAGCGTATGACAGC | 11059 |
rs528049179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463957 | TCCCAGCTACTCTGG[A/T]GGCTGAGGTGGGAGG | 11059 |
rs528060143 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86413550 | TCGAAAGCTATGACA[A/C/T]GTCAGTGGATTCTGA | 11059 |
rs528134424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456716 | GTTCATTAACAAGTG[A/C]ATGGATAAGCAAATT | 11059 |
rs528139961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364552 | TAAAAATAAAAAATA[C/T]TTCAGTGCTTTGGGA | 11059 |
rs528156078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448950 | GCAATTCTGCCTTAG[C/T]CTCCTGAGTAGCTGG | 11059 |
rs528156994 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86457433 | TCTGTCTGTCTGTCT[A/G]TCTATCTATCTATCT | 11059 |
rs528240004 | in-del | -/AAAT | 0.00161388 | 0.0283608 | intron-variant | WWP1 | GRCh38.p7 | 8:86451051 | ACCTCATCTCTACAA[-/AAAT]AAATAAATAAATAAA | 11059 |
rs528244006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449640 | TGACGCATCTTAAAA[G/T]GTAATGGGCCTAAAA | 11059 |
rs528267532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86349406 | AGCAAGTCACAAATC[C/T]AGCCCAGGTTCAAGG | 11059 |
rs528268142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357771 | TCAGCAATTTATTTC[A/G]GAATTTTGCTTTGAT | 11059 |
rs528277278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86442526 | CTTAAAGACTGTTGA[A/G]CAGAGGTATGATGTA | 11059 |
rs528322337 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343597 | CTCCTTACCTTTACG[A/C]CCTTTAAATGATCAG | 11059 |
rs528401872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435295 | TAGTCCCCATTACTT[A/G]AGCTTCTTTTGGCCC | 11059 |
rs528440148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379120 | ATAAGACTTACATAT[A/T]CTGAGGAAATATATG | 11059 |
rs528519063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421315 | CTTAAGCATTTTGTG[A/G]CTTAGGTTTGTTAGA | 11059 |
rs528525161 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86376979 | TGTCAGTGAGGACAC[-/G]TGAGAATCAGAGGGA | 11059 |
rs528527309 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467650 | AGATGCTAGGTATTT[A/G]TGGAATTAAAAAGAA | 11059 |
rs528574199 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86431308 | TCCCTGATATGTTTT[-/TA]TATATATAATATATA | 11059 |
rs528601135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86373152 | TAAATTCTATTTATA[G/T]TTTTCAAATTTATCT | 11059 |
rs528620119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466211 | GTATTTTAAAATTTT[C/T]ATCAGTTAATACCAG | 11059 |
rs528624135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86366306 | ATAGATGCAGAGGCT[G/T]TGATGGCTTGGGGTA | 11059 |
rs528640054 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355039 | AAATATGCACAAATA[A/G]AGTTGAAGTTTGCAT | 11059 |
rs528643592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458229 | TTGCTGAAATGAAGG[A/T]GTTGAGTGACAGAAT | 11059 |
rs528709376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367130 | ACTGCTCTGTTACAT[A/G]TCATCCTATCTTGTT | 11059 |
rs528730014 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86450579 | GTATATTCACTTTCT[A/G]TAAAGTTAAGCACTG | 11059 |
rs528746096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359531 | TGTCTCCTACTTCAC[C/T]GAGAAAATTGGAGAC | 11059 |
rs528757148 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443217 | AGCTGAGACTACAGG[C/T]TCACACCACCATGCC | 11059 |
rs528761451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408866 | AGTGAGCTGAGATCG[C/T]GCTACTGCACTCCAA | 11059 |
rs528805855 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466244 | TGGAATTGAGTATGG[C/T]AAGATTGAAAAAGTG | 11059 |
rs528845652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462586 | AATCCCAGAAAAATC[A/G]GCCAGAAAACAGTAT | 11059 |
rs528853174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370527 | TCTTTACTGGGCTTC[G/T]GTAATTGTTCGTTGG | 11059 |
rs528899781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86419350 | TTGAACCTGGGAGAC[A/G]GAGGTTGCAGTGAGC | 11059 |
rs528915526 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405921 | ATTGTGGGTCAATAC[-/T]TAAGGGGTTTAAGAC | 11059 |
rs528927270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363200 | TTGTGAGATGGGGAC[G/T]AGGAAACAACAACAA | 11059 |
rs528941378 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | WWP1 | GRCh38.p7 | 8:86371117 | TTGACCTCAAGTGAT[C/T]CACCTTGGGATCCAC | 11059 |
rs528992695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463853 | ATCGCTTGAGCTCAG[C/G]AGTTCGAGACCAGCC | 11059 |
rs529006500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456647 | ACACAAAGACTCATA[C/T]ATACATGTTAATCAT | 11059 |
rs529019317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413524 | TGCGCCGTTGACGTC[A/G]AAGAATACTTTCGAA | 11059 |
rs529045549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405666 | CCCCCTGAATAGTTG[A/G]GACTATAGGCATGTG | 11059 |
rs529046145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364283 | CTAATAGTTTAGAGT[A/G]GGTGGGTCATAGAAT | 11059 |
rs529053638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355899 | TATATTTTGTTTCTG[C/G]AGTGCGTATGTAGTG | 11059 |
rs529095689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86358709 | AGACAAGGTTTTACC[A/G]TGTTGCCTAGGCTGG | 11059 |
rs529108496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349333 | CTGCAACCAGATCTT[A/C]TTAAGGTTTAGACTT | 11059 |
rs529116945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440883 | GTTTTGCTGCTTCTA[A/G]TGTGATTTTTCTTCA | 11059 |
rs529126367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86385147 | CCTATCCTTAAATTC[C/T]GATTTGAGGGGCAAG | 11059 |
rs529149247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391725 | GGCTCAGTAGAGTCA[A/G]GAAAATGAAAAATTA | 11059 |
rs529162975 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WWP1 | GRCh38.p7 | 8:86348465 | ACAGGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA | 11059 |
rs529164527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86441700 | TTGTCTGAGGACTAC[A/G]ATAATATGCCTAGAA | 11059 |
rs529169806 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342412 | GGCCCCGCCCCTTCC[A/G]CACGTTCAGGCCCCG | 11059 |
rs529176071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399224 | AAATAGGTATCATAC[C/T]GCTCTCTGGATTGGC | 11059 |
rs529187367 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413060 | TCTCGAACTCCTGAC[A/C]TCATGATCCACCCGC | 11059 |
rs529200011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392142 | TTTAGTGTGTGTGCA[A/G]TGGTGGTAGTGGTGC | 11059 |
rs529266316 | snp | C/G | | | downstream-variant-500B, missense, stop-lost, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468696 | ATGCACTAGGTGAGG[C/G]TACACAGAACCCTAC | 11059 |
rs529281941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378168 | TGATTTTTCTTTGGC[C/T]TTTATTTGAATATTT | 11059 |
rs529287652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386375 | CATTGTGTCTGTGTA[C/T]AGTTGCTGTACCCTA | 11059 |
rs529307009 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86387186 | TAAATTATTTTTATT[C/G]GTTGCCATATATATA | 11059 |
rs529387939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378982 | TGGAGAAATTAATTG[A/G]CTTACTGTGGTCAGG | 11059 |
rs529397500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427299 | GGGCTTAAAACCTAG[A/G]TGATGTGTTGATAGC | 11059 |
rs529399550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420308 | TATGCAACTGGAAAA[C/G]TATTTGGGGTTTAAC | 11059 |
rs529407732 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384146 | TCATTGGATTAGGGC[C/T]TACCCCAATGACATT | 11059 |
rs529438072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421162 | ATTGTCTGATTTTAG[C/T]GAAATGCTTTATAAG | 11059 |
rs529439522 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433921 | AAACTCCATCTTAGG[-/A]AAAAAAAAAAAATGT | 11059 |
rs529505953 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389744 | GGCCGGGCAGAGGCG[C/T]CCCCCCACCCACCTC | 11059 |
rs529506514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414358 | GGTCAAAAAAAGTTT[A/G]AAAGCCACTAATCCA | 11059 |
rs529514072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447919 | GTCTTTTATCATCCT[A/G]TACAGTTTTTGATAT | 11059 |
rs529516090 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86415042 | ATATGTACCTCATGC[C/G]GTATACCAAGGAGGC | 11059 |
rs529548242 | snp | C/T | 0.000169704 | 0.00920996 | intron-variant | WWP1 | GRCh38.p7 | 8:86458067 | AAAGTACTCAACATA[C/T]TTTCTAATGAAATGG | 11059 |
rs529549291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86407152 | GGTTTGCATAAGCTT[C/T]TGCTATCATAACTAT | 11059 |
rs529625416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400767 | CAGTAAAATCGATTA[C/T]CTGCTGCAAAGTGAG | 11059 |
rs529669727 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454714 | GAGATGAAACTAAAA[C/T]GGGAGATCAAGAAGC | 11059 |
rs529686832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450410 | TATTCATCAAAAGAT[A/C]ATGCATAAGGCACTG | 11059 |
rs529699502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350680 | AGTTAAAAAATATCC[C/T]AGCATTAACAGAATG | 11059 |
rs529710470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393465 | GTTGGCTAGGCTGAT[C/T]TTGAACTCCTCAAGT | 11059 |
rs529712220 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86401354 | CGCTTGAGGCCAGGA[A/G]TTTGAGACCAGCCTG | 11059 |
rs529723968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443453 | AAGCGCTTTGCAGAA[A/G]CCCTTATGGAACTAT | 11059 |
rs529725818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451074 | AAATAAATAAATAAA[A/T]TTTTTTTAAAAAATT | 11059 |
rs529737692 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86458645 | TACTCTACTAATTGG[G/T]ACTCTTTTGAGCAAC | 11059 |
rs529750616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351430 | AGCAGGCTTGACCTC[A/G]GGGGCTCAAGCAATC | 11059 |
rs529770428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344302 | CTGCTGGTAAGATCT[A/T]CATCAGGGTTTTGAA | 11059 |
rs529811526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444391 | GGTATAAGTCTGGCA[A/G]TGAAAGGATATTTAG | 11059 |
rs529855151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344489 | GTATTTTGGGAAATA[A/C]AAAGATGAACCGATT | 11059 |
rs529878593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381059 | AATGCTTGCTTTTGC[A/T]TTATAAACCAAATTA | 11059 |
rs529968317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86415916 | CAAAACTATGCCTAC[C/T]GTATAGCAGGCACTC | 11059 |
rs529993011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430091 | GTAGTCCTAGCTACT[C/T]GGTTGTTGCTGAGGT | 11059 |
rs530007682 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466717 | CCATTCAGCATTTCT[A/G]TGTGCTTTGAAAAGT | 11059 |
rs530021486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381708 | TGAATCCTAAAAGCA[A/G]AAACATAGTTTTGTA | 11059 |
rs530035976 | snp | A/C/G | 0.000217206 | 0.0104191 | intron-variant | WWP1 | GRCh38.p7 | 8:86374172 | ATGAACTTTTCTTTT[A/C/G]AATACCTAATTCAGC | 11059 |
rs530051544 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349668 | AAATGGGAATACCTA[A/G]CACTCTCCTTGGTTA | 11059 |
rs530052728 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416519 | CAGAAGTTGCCCAGT[A/C/T]GTTCACCAAATTTTA | 11059 |
rs530074386 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374777 | TACGGTGGCGCAAAC[A/C/T]TACCTCCTTGTAGCC | 11059 |
rs530074440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367468 | CAGGCAATTAAGATA[C/T]GCCTTCTAAATGAGG | 11059 |
rs530087857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459772 | GGTGTTCCATGGCTT[C/T]CTGTTTACACATTTG | 11059 |
rs530107344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86377147 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 11059 |
rs530119081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86451970 | AGTTAGGAAATCTTC[A/G]TGTTTTCCAATAAAA | 11059 |
rs530119777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360385 | GTGGAGTTGGTCACT[C/G]TTTCCTCCTCCTTGA | 11059 |
rs530154535 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86355793 | CAAAACCACCTGACG[-/T]TAAGCTTTAGTTGAT | 11059 |
rs530167654 | in-del | -/ATATATATATATATATATATATATATAT | 0.0185938 | 0.0946107 | intron-variant | WWP1 | GRCh38.p7 | 8:86362164 | ATATATATACAAGGC[-/ATATATATATATATATATATATATATAT]ATATATATATACTGG | 11059 |
rs530178421 | snp | C/T | 1.71358e-05 | 0.00292704 | intron-variant | WWP1 | GRCh38.p7 | 8:86402214 | CACTGGTAAGCAAGG[C/T]TATTTATGACACCTT | 11059 |
rs530186425 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408407 | TTTTAAAGTATGTTT[A/G]CTTTTGTAACAAACG | 11059 |
rs530196465 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86460833 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 11059 |
rs530204690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452916 | GTGTCACTTGTTAGG[A/G]GTCTTGAAGAGTTGT | 11059 |
rs530206912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445339 | CAACCCTTGCCTTCC[A/T]CCCTCTCTCCCTCCC | 11059 |
rs530212022 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86352212 | GCGACACCTAGCTAA[C/T]TTTTTATTTTTATTT | 11059 |
rs530285635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346424 | CGAGACTCTGTCTCA[A/G]AAAAAAAGAACTTTA | 11059 |
rs530286034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86361105 | GAGTTACCTTCATGT[A/G]TCCTGCTTTAGAAGG | 11059 |
rs530296503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402879 | TGGTTCTTTTATCCC[A/G]TCTTTCAGTATACAA | 11059 |
rs530326385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437990 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 11059 |
rs530359883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86352886 | TCAAAACATTTCCTC[C/T]GTACTTCTTTCTACA | 11059 |
rs530360650 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86430939 | TATATTCTATATATT[A/C]TATATTCTGTAGAAT | 11059 |
rs530387579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86395561 | GGGTTAAACCCTGAC[C/T]AGCCTAAAGAAGACC | 11059 |
rs530405591 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460941 | CAGCCTCTCGAGTAG[C/T]TGGGACTACAGGCGC | 11059 |
rs530438274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86386995 | GGGCACACCCACTCA[C/T]TCAAGTCCTTTTATA | 11059 |
rs530472510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457548 | TATACATAATAGATA[A/C]ACACACACATTTAGA | 11059 |
rs530487213 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | WWP1 | GRCh38.p7 | 8:86400117 | GGGCAGATCATGAGG[G/T]CAGGAGTTCGAGACC | 11059 |
rs530502010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450369 | TAGTTGGAAAAAAAC[A/G]GTAACACTATATTTT | 11059 |
rs530520789 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86400518 | TTTGAGCTAAGATTA[A/G]TAAGCCACAAATGAA | 11059 |
rs530571183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449723 | TAGTACTACCATTTT[C/T]ACCCTCTTAGATGCT | 11059 |
rs530580825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350175 | TTCTCCTTTCCAAGA[A/G]CAGGTAGATTCATTG | 11059 |
rs530608761 | snp | A/G | 2.71706e-05 | 0.00368572 | intron-variant | WWP1 | GRCh38.p7 | 8:86442607 | AAATAACCTTGACTT[A/G]TTTTCTTATAGAGAA | 11059 |
rs530620832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435334 | TGTATACCCTTCTCT[A/C]CCAGCAGAAATCTTC | 11059 |
rs530645715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388080 | TTAAATAGCCATACA[C/T]GGCCGCTGGCTACTG | 11059 |
rs530652093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344233 | TATGTGGAATAGTTC[C/T]TTGGGACATAGCTTA | 11059 |
rs530653033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343789 | TTTTCTATTTGATAA[A/G]TTTAACAAATTTTTT | 11059 |
rs530664532 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369703 | GTTTAATCTACCTCC[A/G]TATGAATCAATATCT | 11059 |
rs530673459 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401822 | TAAAACATGTCATAT[A/C]TTTGTTCATTACTCT | 11059 |
rs530715769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387485 | CACATTCATATATGT[A/G]TATTTATTTATTTAT | 11059 |
rs530741456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429218 | GTTGCAAGCCCTTGC[A/C]TTTTTTACTTAGCGA | 11059 |
rs530789264 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436334 | TAGATACTGTATTCC[A/G]TTTGAGAATTCCTTT | 11059 |
rs530824080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422595 | TCAGGCTGGTCTTGA[G/T]CTCCTGACCTCAGGT | 11059 |
rs530844407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86380173 | GGTATTTGGCAAGAA[A/G]AGGAGTGGAGTACTG | 11059 |
rs530860119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415804 | CTTTATTATTTTTCT[A/G]GCACTTAAATTATGT | 11059 |
rs530882057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86380922 | TGTATTTTTTGGAAT[A/G]TGTTTTTTGTTTTGT | 11059 |
rs530888470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367341 | TTCAAAGTCTTAACA[C/T]TGCAGAGTGTGCAGA | 11059 |
rs530889379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373232 | ATTTTTTGAAATTTA[A/G]TGAGATTTTCATTAT | 11059 |
rs530927432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458989 | TTCTTTATAAGTCTA[C/T]ACCTTGGAGTCATTC | 11059 |
rs530949832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86415268 | TTTCCCCACATTTCC[A/G]TATCCTGCTTTATTT | 11059 |
rs530961757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451349 | AAGTTGATGGTGAGA[A/G]TTAGTGGCTATAGTG | 11059 |
rs530977471 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86366415 | AGATCAGTGGTGATG[A/G]TATGGACAGAGAGTC | 11059 |
rs530979861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359571 | CATTTCCTTAACTTT[C/T]TTTCCAGACATTTTC | 11059 |
rs530997488 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352294 | CAGTGGCGCTATCTC[A/G]GCTCACTGCAACCTC | 11059 |
rs531069807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86352196 | AGTACAGGTGTGTGC[C/T]GCGACACCTAGCTAA | 11059 |
rs531087782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445128 | CAGCTCTGTAGGGAA[C/T]TAATAGAGTGAGAAC | 11059 |
rs531113985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401711 | ATTATTGTGGGAGAC[A/C]GTATTTATTTTGACT | 11059 |
rs531121340 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466078 | TCACTGCTACTGTAG[A/G]GACCAAAACCCTGAA | 11059 |
rs531122001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394795 | TGATCCAAAATGTTA[C/T]AACTCAATCTTCCAT | 11059 |
rs531130335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345423 | GCTTTTTTTATTTTC[A/G]AGGCAGGATTTCTTT | 11059 |
rs531138772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360258 | GGTTTTTTTTGCTTG[G/T]TAAGCCACAGGCTTC | 11059 |
rs531176885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437115 | TCTATTTGATGTATA[A/G]CACTGAGCCCACGAC | 11059 |
rs531181345 | in-del | -/GAAA | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86425583 | TGTAATTTTTTTAAG[-/GAAA]GAAAGGTAGTATTTA | 11059 |
rs531186953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464665 | GGACCACCAGTGCAC[A/G]CCACTATGCCTGGCT | 11059 |
rs531206296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389729 | CTTCCCAGACGGGGC[A/G]GCCGGGCAGAGGCGC | 11059 |
rs531220091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366531 | GTAGTTCCAGTGATA[C/T]GATTTTGAGCCTTAG | 11059 |
rs531241452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382059 | AGAAGATAGACAATT[A/G]TAGAGTAATATAAAA | 11059 |
rs531303049 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86409028 | TCTAATGGGGTTTTT[-/A]AAAAAAATTTTCTTG | 11059 |
rs531322335 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86375021 | TCCTCTTAATCAAAA[A/G]ATCTCCATTCAAAAT | 11059 |
rs531391639 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467305 | GCTCCATGTTCTTCT[C/T]TCCCTTATGTAACAT | 11059 |
rs531403246 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413757 | GAAGAGAAAACAGCC[C/G]TGTGAAGAATTTTGT | 11059 |
rs531409493 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363512 | AGAGGTTAAATTATA[C/T]GTCTATGGGCCGAGC | 11059 |
rs531420120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417292 | TATGTAAGTACCTAC[A/G]TAATCATCTTGATTA | 11059 |
rs531422895 | snp | A/C | 0.00205273 | 0.0319711 | intron-variant | WWP1 | GRCh38.p7 | 8:86430791 | ATAAGGGAGATATAT[A/C]TCTCTCCATATATAT | 11059 |
rs531423234 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86423830 | CCCCCCCACCTCCCG[C/G]ACGGGGCGGCGGCTG | 11059 |
rs531442691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375949 | AAGCTTTGGGATTGT[A/T]CATAATTAGACACTG | 11059 |
rs531458393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410438 | GTATTTCTAATGTTA[C/T]TTATATTAAACATGT | 11059 |
rs531487216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361339 | GTAGTCCACCACTTA[G/T]AGATTCTGCTCCTCA | 11059 |
rs531594276 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394666 | TTGAATGGATAAATA[C/T]ATCGGAGTTGGTTTG | 11059 |
rs531615102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369497 | AAAAATAGATTGGGG[G/T]TGGGGATCAGGGTAC | 11059 |
rs531633204 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352441 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGGCC | 11059 |
rs531670089 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425655 | TAAACTATGTTATTT[C/T]ATAAGATTTAATGAC | 11059 |
rs531688230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453804 | TTTGCATTTCCCTAA[C/T]GATTAGTTATCAAGA | 11059 |
rs531699415 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86362099 | ACACATATATATATA[C/T]ACTAGGCATATATAT | 11059 |
rs531704503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397259 | AGATCAGATGGAAGT[A/G]TTTGGCCTCAGTTTG | 11059 |
rs531719571 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86353223 | AAATTTCAAGCTAAT[C/T]TCTAACTGTTATTTA | 11059 |
rs531722095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390443 | TCCGTCTGCAATCCC[A/G]GCACTTCGGGAGGCC | 11059 |
rs531728555 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86350602 | GGCACAAAGAAGGGC[A/G]CGGATAGAGTTACAT | 11059 |
rs531758200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86432329 | AAGTTGTACCACCAT[A/G]TCTGTCCGTCTCCTA | 11059 |
rs531784768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353849 | TTTTGAGGAAAAACA[A/G]CAGCCATCTCTTTTT | 11059 |
rs531810818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383588 | GTCTACCAAAAATAC[A/C]AAAATTAGCTGAGTG | 11059 |
rs531897718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439751 | TTTCAATTTTGTCCC[C/T]TATTTGTTCTGCCCC | 11059 |
rs531905363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433485 | CTGGGAGGTTGAGGC[A/G]GGTAGATCACTTGAG | 11059 |
rs531922673 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443784 | TGAATCATGCAGATA[C/T]CTTGGAGACTATTCT | 11059 |
rs531933683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385119 | ATATTCAGTACTAAA[A/G]ACATTTTTTGTTCCT | 11059 |
rs531941223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418823 | GTAAAGTAAATTTTC[A/G]AATACACACCCAACA | 11059 |
rs531966298 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341048 | TGAACGGGGAGGAAA[C/T]TGAGCAATGAGGGGA | 11059 |
rs531968221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86384302 | ATAAATTTATTTGAA[A/G]AATTAAATCTCATGA | 11059 |
rs532004316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86394161 | GCAGTTTTTAAAAAC[A/G]GCTTCAGAATGTGGC | 11059 |
rs532055994 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364806 | AGTGAGACCCTGCCT[C/T]GAAAGAAAGAAAGAA | 11059 |
rs532094386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389692 | CCCAGACGGGGTGGC[A/G]GCCAGGCAGACGGGC | 11059 |
rs532116379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444435 | ATTTGGGAATTCTTG[G/T]CACATAGAGAGTATT | 11059 |
rs532145518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430169 | TCACGCCACTGCACC[C/T]CAGTCTGGGTAATAG | 11059 |
rs532153077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445060 | GTGTATGAAAGTCAC[A/T]TGATGAGAGAGGAAG | 11059 |
rs532155483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86436403 | TGATCTCAGAGAGAC[C/T]TTCTCTGAGCCTACT | 11059 |
rs532161135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394669 | AATGGATAAATACAT[C/T]GGAGTTGGTTTGTTT | 11059 |
rs532228650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86423796 | ACTTCCCAGAAGGGG[C/T]GGCCGGGCAGAGGCG | 11059 |
rs532235013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416680 | TAAACACTAGGTAGA[A/G]GAGGGTTATGGTTGA | 11059 |
rs532246878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374890 | AATTTAAAAAAAAAT[C/T]TTTTTAGAGACAGGG | 11059 |
rs532285875 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366723 | GTTCACTAGGATTAT[A/C]AAAAATCCCAGTTTG | 11059 |
rs532311910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409669 | GTTCAAGACTGGCCT[A/G]GCCAACAAGGTGAAA | 11059 |
rs532316936 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414039 | TGTTGTCACCACTTA[C/T]GATCTTTGTATTAGA | 11059 |
rs532321707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417084 | CAGCTGCCAGGGGAG[G/T]AGAGAAGGGCACACA | 11059 |
rs532342372 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456918 | GACATTCTTAAAAGG[A/C]CAAATATAATCTGTG | 11059 |
rs532366386 | in-del | -/AAA | 0.00462158 | 0.047848 | intron-variant | WWP1 | GRCh38.p7 | 8:86442842 | TTAGAGAAGGCTTTT[-/AAA]AAAAAAAAAAAGGAT | 11059 |
rs532397997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424118 | GCAGAGGGGCTCCTC[A/G]CTTCTCAGATGGGGC | 11059 |
rs532410403 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409526 | GGCGTGAGCCACTGT[G/T]CCCAGCCCTGATTTT | 11059 |
rs532455262 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467206 | TATAGAGCTCCAAGT[A/G]TATTAAACATGACAG | 11059 |
rs532464566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402980 | TTTCCAAAAGTAAGC[A/G]TTACTGTATTATAGA | 11059 |
rs532465571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460036 | CTATTTTTAAGATAC[A/G]TTTCCACTCTTAATC | 11059 |
rs532466397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397672 | TTTAATGCATAGTCT[A/G]AATATATAGTCTAAC | 11059 |
rs532478923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445785 | GAACAAAGTATATGT[C/G]TCTTTTTTTTCTGAA | 11059 |
rs532501258 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86395768 | AGAATTAGTAATAAG[A/T]GAAGATAGTGGAAAA | 11059 |
rs532504866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86460902 | ACAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 11059 |
rs532513484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360521 | CAGTAGGCCTTTCCT[G/T]AGTGGGTACCTGTCA | 11059 |
rs532621326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453688 | AGTTTCTCCACATCT[C/T]TCCCAACATTTATTT | 11059 |
rs532642376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403748 | GCTCCCCTTAAAAAA[A/G]AAAAAAGAAGTAGAC | 11059 |
rs532647890 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349426 | CAGGTTCAAGGGTAC[A/T]AATGTGTGAATCCAT | 11059 |
rs532664316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432240 | GTTGACAGATCTCTC[C/T]TTCATTCTTACTCTA | 11059 |
rs532702320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432616 | AGTTCATTTTTTTGT[G/T]TTTTTTTTGAGACGG | 11059 |
rs532711176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446340 | CCCAGTTTTTAATGG[G/T]TTTTTTTTTCTTGTT | 11059 |
rs532727389 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86353639 | CTGGGATTATAGGTA[C/T]GTGACACCTGCTGGC | 11059 |
rs532741324 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86390114 | GCGGCGGGGCAGAGG[C/T]GCTCCCCACATCTCA | 11059 |
rs532743894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376214 | AGGACCAATGGACAG[C/T]ACACCTGAGGTGTAA | 11059 |
rs532750555 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468106 | CTTTTAGCAAACTGG[A/G]CTTCCTAATACAAAA | 11059 |
rs532778983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347014 | ATTTTATTTTATTTT[A/G]TTTATTTATTTTTGA | 11059 |
rs532849695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86412406 | GATTTTCTTTAAAGA[A/G]TATTCTATATGTGTA | 11059 |
rs532887309 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444822 | AACTGGAAATGCTTA[C/T]GGAGTCAAGAATGGG | 11059 |
rs532914836 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86409620 | ATCCCAGAACTTTGG[A/G]AGGCCAAGTTGGGTG | 11059 |
rs532961178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363639 | AAACCCCGTCTCTAC[A/G]AAAAATAAACAAATT | 11059 |
rs532982270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376688 | AACCAGTTGGAAAAT[A/T]GATGTGGACCAAGGC | 11059 |
rs533014198 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413468 | AAGTTTAGGATGCCA[C/T]GACAAGGAATACATG | 11059 |
rs533021163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370265 | AAACATTTAAACATC[A/G]TAAAAGATGTTTGAG | 11059 |
rs533022161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86447384 | CAATTCTCCTGCCTC[A/C]TCTTCCTGAATAGCT | 11059 |
rs533033835 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446848 | TTTATTTAGCACACA[A/C]ACCAAGTGATGGAAA | 11059 |
rs533089587 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388708 | TAGTTTTCACAAAAT[C/G]ATTTCTTTTATAATA | 11059 |
rs533108541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412461 | TTTGGCACTGATAAT[A/C]CTAATATTAATTAAT | 11059 |
rs533148014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86412895 | GTGCAATGGCACGAT[C/T]TTGGCTCACTGCAAC | 11059 |
rs533176705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86441431 | AACCTTTAGAAAAAC[A/G]TTTATTAACAGGCTG | 11059 |
rs533211731 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446136 | ACAGGCACGCACCAC[C/T]ACACTCAGCTAATTT | 11059 |
rs533233582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448088 | TTTTCTTTTATCATT[A/G]TTCTCTAAGAAATTG | 11059 |
rs533258256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398152 | TATGCACAGAAGCAA[C/T]TAAAGGTGATATTGA | 11059 |
rs533258555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426083 | TTTTATGGGATATTT[A/C]TCTTTTATGGAATAA | 11059 |
rs533264015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386273 | TTATTATGGAGAGTG[G/T]GTAAAAATTATATCT | 11059 |
rs533265775 | snp | A/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342379 | GCTTAGAGCAGCCTC[A/T]TCCCAAATCTCAGCG | 11059 |
rs533281459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348450 | CTTGAACTCCAGACC[A/G]CAGGTGATCTGCCCG | 11059 |
rs533349400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391508 | ATTTCTTAAACTACA[C/T]AGGAAAAAAAAAATC | 11059 |
rs533366893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433682 | GTTATGGTGGCTCAC[A/G]CCTATAATCCCAGCA | 11059 |
rs533420156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86420820 | CTATCTGAAAGTATA[C/T]GTAATTTTGATAAAA | 11059 |
rs533434586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372384 | AGGCGGGTCTTGAAC[C/T]CCTGACCTCAGGTGA | 11059 |
rs533493481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426833 | CAGATTGCTTGGTAT[A/G]CAGCAAGCACTGTCA | 11059 |
rs533505332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86414276 | GTAAGTAAAATCAGT[A/G]GATAAATAGCAATCT | 11059 |
rs533524876 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466977 | TGTATATAAGCTGTT[A/C]ATTCTGTACAGTGAA | 11059 |
rs533531986 | in-del | -/AACGTTT | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86420274 | CAGCTAATGAGCTTG[-/AACGTTT]TAAGAGGAGATTTAT | 11059 |
rs533568999 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364015 | AACCCTGATAAGAAG[A/C]GCACATTAAATTGCT | 11059 |
rs533586591 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86420221 | ACAGCACTCACTCTA[C/G]ACTAGAAGCTAATCA | 11059 |
rs533593949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464103 | TGCAAGAAGAGGAAA[C/G]AGTAGATTTTGTATA | 11059 |
rs533627447 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86394823 | CATGTTCAGAATTGT[G/T]AAATAATATATACTG | 11059 |
rs533645292 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391432 | TTTTAGCTTTCTTTC[C/G]CTTATGTCACCAGTG | 11059 |
rs533655799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86364677 | CAGGCATGGTGGTGC[A/G]TGCCTGTAGTGTCAA | 11059 |
rs533664596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368737 | AGCAGTTCTCTGGAT[G/T]TGCCGTTCTTTCTGT | 11059 |
rs533668743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86356381 | GGAGTGGGAAACCTG[G/T]TTTCTGATGTTCACT | 11059 |
rs533669482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452420 | TATGTATTCATACAT[A/T]TACACACACATCACA | 11059 |
rs533673773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360853 | TGGCCTATGGTGATC[A/G]GGAATTCTTTCTGAA | 11059 |
rs533700195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361369 | AATACCTCTGCTGCT[G/T]CTTCTCTTTCCCCTA | 11059 |
rs533736932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86352587 | CCAGGCTGGTCTTGA[A/G]CTCCTGGACTCAAGT | 11059 |
rs533777183 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444169 | GTGAGAAGTGATTTG[G/T]ATTCTGGGTATATTG | 11059 |
rs533779974 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86375067 | TCTGTTTTTATCCTA[C/T]TACACCAGTTCAAAA | 11059 |
rs533790696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416861 | GTACAGCTCTAGCAG[G/T]CTGTCACTGTGAGTC | 11059 |
rs533805276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396008 | AGACACTTGAAATCA[C/T]GAGAGATGACAAGAA | 11059 |
rs533905205 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419307 | CCTGTAGTCCCAGCT[A/C]CTCAGAAGGCTGAGG | 11059 |
rs533908918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86460971 | CCCGACACCACGCCC[A/G]GCTAATTTTTTGTAT | 11059 |
rs533924074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390474 | CAGGCTGGCAGATCA[C/T]TCGCGGTCAGGAGCT | 11059 |
rs533939395 | in-del | -/AAAC | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86391541 | TCTATTGTTACAGAT[-/AAAC]AAAGCTGGACACTGT | 11059 |
rs534023091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446086 | TCCTGGGTTCAAGCA[A/T]TTCTCTTGCCTCAAC | 11059 |
rs534033989 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445441 | GTACGTAAGAACATG[A/C]AGTATTTGGTAGTTG | 11059 |
rs534058495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86346688 | ATAAACTTTGATTTC[A/G]TAATTATTAGAAAGA | 11059 |
rs534062426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418178 | CAAATATTTAATCGA[C/T]AAATATTTATTAAAC | 11059 |
rs534063177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438504 | GTGTTATTTTGAAAA[C/T]AGAGATTAAATTTAA | 11059 |
rs534084132 | in-del | -/TC | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86452297 | ACCTCCTATTTATTT[-/TC]TTTCTTTTTTCTGTG | 11059 |
rs534097464 | snp | A/C | 0.000165322 | 0.00909031 | missense, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466852 | CTAAAGGAAAAACTT[A/C]TTTTTGCAATAGAAG | 11059 |
rs534117174 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434958 | TTCCTAGGTGCCGTG[C/T]CACCAACTCTGCCTT | 11059 |
rs534144947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418980 | CATTATTATCACTCT[G/T]TAATTAATCCACAAT | 11059 |
rs534152320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86439242 | CAGCTACTCGGGAGG[C/G]TAAGGCAGGAGAATG | 11059 |
rs534181053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412569 | AGAAAGTATATATGG[A/C]CACGTGCTTTCCAAC | 11059 |
rs534210977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432380 | TCCTATAGATGAACT[A/G]TCATTGTTATTATCA | 11059 |
rs534226138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383714 | CCACTGCACTCCAAG[C/T]CTGGGCTACAGAGCG | 11059 |
rs534260255 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364491 | GAGGTAATGTACTGT[A/G]AAGCAGAAGAGTTTT | 11059 |
rs534278045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447624 | AGTAAGGGAAGACAT[A/G]ACTTCATGAGGGGGC | 11059 |
rs534280408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456027 | GGGAATATCTTTTCA[A/G]CAAATGATGTTGAAT | 11059 |
rs534302853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86405807 | AAATTGTTGGGATTA[C/T]AGGGGTGAGCTACCA | 11059 |
rs534306859 | snp | C/T | 0.000190531 | 0.00975853 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468343 | AATTCATAGTAAAGA[C/T]GAAAGAAAGGCAGAG | 11059 |
rs534316174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376385 | ACTGGCCTGGCCAAC[A/T]TGGTGAAACCCCATC | 11059 |
rs534429503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370559 | CAAACTCTTGAGGCT[C/T]AGGATCCACAGTACC | 11059 |
rs534431957 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378293 | ATTGAAATATTTCAA[C/T]GTTAAACTTTTCAAA | 11059 |
rs534433280 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86362706 | AAGATGACAGTGTGT[A/G]GGTATACCACTTCAG | 11059 |
rs534435122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430568 | AGGCATGAGCCACTG[C/T]GCCCAACCCCTTATC | 11059 |
rs534435940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462692 | GACATCCTAGAGATA[A/G]GTGATTCTTTCAAGA | 11059 |
rs534484199 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342055 | ACTTTGTCAGATTGT[C/T]GTGTGCGTTAATTGT | 11059 |
rs534590679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397915 | CCATTGTCTCCATTT[C/T]GTAATTAAGAAACCA | 11059 |
rs534612145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347695 | ATCTGGAAAAGTACA[C/T]TGGTGAAATGTAGAT | 11059 |
rs534663768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372108 | GACTCACTGCAAGCT[C/G]CGCCTCCCGGGTTCA | 11059 |
rs534674374 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86391145 | TTCCCCAGAATCCAA[C/T]TAACTGCGTCTTGTT | 11059 |
rs534713033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391764 | TGGTCAGTGTAAATG[C/T]AATTAGGCCCTTGTG | 11059 |
rs534744112 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366078 | TATTAATGACATTGC[C/T]AGTAGGTCCCCTACA | 11059 |
rs534771022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365827 | GCTTTAAAAGAAATC[A/T]CATAGCTTCTTTCCC | 11059 |
rs534803268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385771 | TTTTTTTCAGTGCTT[A/C]CCACAGTCCACAGCC | 11059 |
rs534824980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457691 | GAAGAATACTCTAAA[G/T]GCGGTTTTTGGTTTG | 11059 |
rs534843218 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86443100 | CTTTTGAGAAAGGAT[-/CA]CACAGTCTGTTGCCC | 11059 |
rs534844626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377647 | AACAGAAAACTACCT[A/G]TTGTCATATAGTAAT | 11059 |
rs534913283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419689 | ATAACAAACACAAAT[C/T]TCTTTATTGAAGAAT | 11059 |
rs534952357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420324 | TATTTGGGGTTTAAC[A/G]ATAAGAATGTAGACA | 11059 |
rs534967587 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379331 | GTTGCCGGTACTTAA[A/G]TATAGTATTTGCTTG | 11059 |
rs534991830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86437893 | CAAGCTCCACCTCCC[A/G]GGTTCACACCATTCT | 11059 |
rs534992284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387657 | AACTGGGGTTACAGA[C/T]GTGTGCTACCATGCA | 11059 |
rs535031924 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86407118 | GTGGGTGTGGTCTTA[C/G/T]GTCTTGTGGAGATGA | 11059 |
rs535040080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413841 | GAATGTAAAGCAGGG[A/G]AGTGGCATAATCCTC | 11059 |
rs535046112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454157 | TCCTTACAATTACAG[C/T]ATATAATAGGATAGT | 11059 |
rs535048375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457186 | TAAGTATTACATATT[A/T]TACTATACCTAAAAT | 11059 |
rs535056359 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463426 | ATTCTCCTGCCTCAG[C/T]CTCTCGGGTAGCTGG | 11059 |
rs535126091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86446941 | AAAAGTTTTCTTCTG[C/G]TTGCTTCTGTTTCCT | 11059 |
rs535135227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449303 | TCCATTTGCCAGCCA[A/G]GTAAGTCCAAACATT | 11059 |
rs535146707 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347229 | CTGGACTCGTGGCCC[A/T]CCCACCATGGCCTTC | 11059 |
rs535156029 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439571 | ATAGATTAGCATGCA[C/T]ACATTCTTATTTTTT | 11059 |
rs535158245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399709 | TACCAAATGTTGTCA[A/G]TTGCATAGTAAGACG | 11059 |
rs535160646 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376616 | AAAAACCTGATCTGG[C/T]TAATTTGAGGTGAAA | 11059 |
rs535207619 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86349772 | CTTCTGCTTGAGGGC[A/T]GTGGGATCTAACAAA | 11059 |
rs535240369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390540 | TCCACCAAAAAATAC[A/G]AAAACCAGTCAGGCG | 11059 |
rs535249242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86458853 | TAAAATATACTTCAA[C/T]GTGTGTAAAGTGGCA | 11059 |
rs535253008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347639 | ATTGTACCACAGAAT[A/G]GTTATTCTCCTGTCA | 11059 |
rs535263798 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463604 | AGCCACCATGCCCGG[C/T]CAATTAGTGGTATTT | 11059 |
rs535274219 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86442884 | ATTTGCTATTCACAA[C/G]TTTTGTTACCAAGAA | 11059 |
rs535286163 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410024 | GAAAATAATCATATG[A/G]CGTTTATCCTTTAAT | 11059 |
rs535313466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435108 | TGTGGTAGAATTTCC[C/T]TCCACGTCTCTTCTG | 11059 |
rs535322741 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342018 | TAGTTGACTTTTCTG[C/T]AAAATGCAGACAGTA | 11059 |
rs535352579 | in-del | -/TGTG | 0.219424 | 0.248123 | intron-variant | WWP1 | GRCh38.p7 | 8:86414228 | GAAAGTTTGTTTTTC[-/TGTG]TGTGTGTGTGTGTGT | 11059 |
rs535364108 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440490 | TTGCTTTACTGTTTT[C/G]TAGCATTGAATGTTA | 11059 |
rs535365455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433775 | ATGGTAAAATTAGCT[A/G]GGCGTGATGGCGTGT | 11059 |
rs535386682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362557 | AGGAAGTGAGTTCAT[C/G]AAAGGAATTTTTTTC | 11059 |
rs535455941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370842 | CATGGTATTGCTTAT[A/G]GCTATATTCATTCTT | 11059 |
rs535503231 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86404964 | TAGCCTTTTCACCAC[C/G]TCTGATTATTGCTAG | 11059 |
rs535573331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371962 | TTCTCCCTCCCTCAG[C/T]GTCCTGAGTAGCTGA | 11059 |
rs535583126 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438145 | TAGAGAAAAGAAAAT[G/T]TTTTTAGAAAATCAT | 11059 |
rs535590025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397718 | AAATGACCTTGAGTT[C/T]AAATAAGAACTAGAT | 11059 |
rs535620532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390936 | ATTTCATGGTTTTTC[A/G]TCTATCTTTTCTGAT | 11059 |
rs535647498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432960 | TACTTGCATGGTTGT[C/G]TCTGTATTGCTGTTC | 11059 |
rs535690491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406569 | TCCTCCAGTGTTAAC[A/G]TCTTGTATAACTATT | 11059 |
rs535709505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384843 | CCATCTCTACCAGAG[A/G]TACAAAAAATTAGCC | 11059 |
rs535743318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425494 | AATCTGTAGGGCTTC[C/G]TCAAGAGACTGTCAA | 11059 |
rs535762900 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396104 | GCTTTTGTAGTTTTC[-/T]TTTTTTTTTTTTGAG | 11059 |
rs535777307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86353119 | ATGATGTGTCTCTTA[C/T]AGGGAAAAGCTTTTG | 11059 |
rs535780077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419145 | CAGACTAGGGCTGGG[C/T]GCGGTGGCTCCCGTC | 11059 |
rs535791320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392445 | TAATTAGACTGAGGT[C/T]TTTTATTTATTTTAT | 11059 |
rs535791337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86400238 | TCAGGAGTCTGAAGC[A/G]GGAGAATTGCTTGAA | 11059 |
rs535827226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392975 | ATGACAGCACCCATT[C/T]GTAAATATTTGCCAC | 11059 |
rs535851505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427062 | CAGCTACCCAGGAGG[C/T]TGAGGCAGGAAAATC | 11059 |
rs535855171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419599 | TTGCCAGACAGTAAC[A/G]CATAAGGACCAGTTC | 11059 |
rs535882483 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373596 | TTTCATATAAATTTG[A/T]TTTTTAAGATTATAG | 11059 |
rs535909935 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452213 | CACATGATATTTGGA[C/T]TTATTTGTCTAGATA | 11059 |
rs535936369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387604 | TGCAGCCTTTGCCTC[C/G]TAGGTTCAAGCAATT | 11059 |
rs535938971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86427559 | ACATGTCTTGAACTT[A/G]ATATTTAAATTGAGT | 11059 |
rs535951046 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465141 | CATTAGAGGAACACG[C/G]CTAAGATTGCTAGGC | 11059 |
rs535965393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363946 | CTTGAAAGGGTGGTT[A/G]GTTAGTTTTGCTTTG | 11059 |
rs535974848 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86421560 | CCGGGCATGGTGGCT[C/T]ACGCCTGTAATCTCA | 11059 |
rs535975729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406022 | GAAGCTTGAGTAAGG[G/T]GATCCATCTGACGGT | 11059 |
rs535976230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379316 | CTCTTTAATTGCTAT[C/G]TTGCCGGTACTTAAA | 11059 |
rs536004518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86356152 | GGAGTCAGAGGCCTG[A/G]TTCAGGTTCCGTGTT | 11059 |
rs536018535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448621 | TTTGGGAAGTTCTTC[C/T]CACCAGTACCAATGT | 11059 |
rs536021357 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86427362 | TGTAACAAACCTGCA[C/T]GTTCTACACATGTAT | 11059 |
rs536026671 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410231 | GTTATAACACCTTAA[A/G]TAACATAAGAATGAT | 11059 |
rs536061153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421892 | GGAAAAGCTATTTGA[C/T]CCTCTCTCAAAATTT | 11059 |
rs536105029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449165 | TAATGGCAGTTCTTT[A/T]AATCTCCTATTTCCT | 11059 |
rs536111154 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424997 | TACTTTGAGTTTCCA[A/G]TACTGTAATAAAAAG | 11059 |
rs536114344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86415363 | CATACACTTCCCACT[A/G]GATTTTACAATTGAC | 11059 |
rs536134265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442085 | AGTGCTGTGTATCTC[A/G]GTATCACCTGCAAAT | 11059 |
rs536176068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458623 | TCAGGGATATTCTTC[A/C]GATAACTACTCTACT | 11059 |
rs536178215 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383884 | TAGCATCCTGCACAC[C/T]TAAGAAGTCGGTAAA | 11059 |
rs536214791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434440 | GTATGCTCTTTTCCC[A/G]AAACTCCATATGGCT | 11059 |
rs536226652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386754 | ATTTTTTCCGTAGAT[A/G]CTGTCTTACTGCATT | 11059 |
rs536232197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343150 | GGTCTTGCCCGGAGT[C/T]CGCCCTGGCAAAGGC | 11059 |
rs536234248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350212 | ATCTGGGTTTTTCTC[A/G]CATTATCACTTAACC | 11059 |
rs536253620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351186 | GCATGGTGGCTAGAA[C/T]GTAAGCCCTTAAATC | 11059 |
rs536291376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444168 | AGTGAGAAGTGATTT[G/T]GATTCTGGGTATATT | 11059 |
rs536311790 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344596 | TTCATAAATGGTACC[A/C]AAATCCTCTCAGAAG | 11059 |
rs536334277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86444711 | AGTTATTCATGAGTG[A/G]TAGGGTGGAAAGACT | 11059 |
rs536349458 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449889 | AATAGCTAGGTACAT[G/T]GTGGTGTATTTTTTT | 11059 |
rs536425946 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434615 | TTCTAGGTCAGGAGT[C/G]ATAAGACATTTGTAC | 11059 |
rs536427855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344980 | GAAACAATTTGAACA[C/T]TTTGTTTCAGAAGGA | 11059 |
rs536428567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389348 | CTTGAGATTAGGGAG[G/T]GTGATGACTCTTAAC | 11059 |
rs536432049 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399850 | TCACAATCATTTCAG[C/T]CTTTACCTGCCCAAA | 11059 |
rs536442984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465271 | CTCGAAAGCAGCAAA[A/G]GTTTTTGAAGAGTGG | 11059 |
rs536445456 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WWP1 | GRCh38.p7 | 8:86380238 | TAATGCTGAGTGAAA[A/G]AAGCCAGTCACAAAA | 11059 |
rs536454762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429675 | TATTAGTGGGCATTT[C/G]TTTTAAAGAAAATTG | 11059 |
rs536467544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414666 | TGGGTGCCTCAATCC[C/T]GTTGATTGTAATGTA | 11059 |
rs536484765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366016 | CTGTTTTCTTGACAT[A/G]ACGTATGTGAAAATT | 11059 |
rs536501971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407362 | GATGGGCACATAGGT[A/T]TCAGAGTTTCTCAAT | 11059 |
rs536517808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86381399 | ATAAATGAAATTCAC[A/G]GTTTTTAAAACATTA | 11059 |
rs536523689 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359392 | TGGGGATTGGTGCCA[G/T]TACTCAGCTGGGCCC | 11059 |
rs536558789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374571 | TAGGAAATGTTTCTT[G/T]TAGAAAGCAAAAAAT | 11059 |
rs536571630 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86396883 | GGATTAGAGGCGTGA[A/G]CCACCGTGTCTGGCC | 11059 |
rs536573957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366554 | AGCCTTAGTGATGAG[C/T]AGTTCCTATCAAATT | 11059 |
rs536608438 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86459032 | TTTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 11059 |
rs536628722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399445 | TAGAATTAACACCTG[A/G]AAATATAAAAATATA | 11059 |
rs536703254 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427162 | GAGCGAAACGCCATC[G/T]CAAAAAAAAAAAAAA | 11059 |
rs536707545 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342801 | CCGGGGCCGACGCCT[G/T]GGTGGCTGCTGCCGC | 11059 |
rs536716214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351699 | CTTAACATGGCTGGC[A/G]ATATATCAGCTAGTG | 11059 |
rs536766437 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455320 | ATATTTTACCAAATA[A/C]CCTAGCCAGTGGCAA | 11059 |
rs536789088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394334 | TAGGAGGTACAAAAA[A/T]ATCAGCTTCTGCCTT | 11059 |
rs536865574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437158 | GGCATGCTGGTGAGC[C/T]GTGCTCCAACCCAGA | 11059 |
rs536909372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464547 | CCAAGATAGAGTCTT[G/T]CTGTGTTACCTATGT | 11059 |
rs536916501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389771 | CCTCCCGGATGGGGC[A/G]GCTGCCCGGCGGAGG | 11059 |
rs536942293 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86423309 | GGACAATAGTGGAGG[C/G]AAGGTCAGCAGATAA | 11059 |
rs536948984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465177 | TGGATTGCTCACTTG[A/G]ATTAGAGCATGAAAC | 11059 |
rs536961550 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86372659 | CATATGGATAATTCC[A/G]GGTTTCTTTAAGTGT | 11059 |
rs536962451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382158 | ATAGACACAAACATA[C/T]TTCTTTTTTGCTTTG | 11059 |
rs536970518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466597 | TATTATTTGTAATTC[C/T]ATTTTCCTCTTGGAG | 11059 |
rs536973373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414609 | TGTTTTCTTTTGTTT[A/G]GTAACTTACTGAGTC | 11059 |
rs537002090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86365943 | AGCCCAATGGGAGAT[A/G]GAAGTGAAAAGTGAT | 11059 |
rs537028710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348624 | GTGTTGAGATGACAG[A/G]TATGAAGCCTTTCCT | 11059 |
rs537081119 | in-del | -/TG | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86406652 | TTCACCATTTCTACC[-/TG]TGTGTGTGTATGTGT | 11059 |
rs537083098 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411928 | AGCAACTCTGTTAAC[A/C]TACGATTATTGAATG | 11059 |
rs537089716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86358077 | ATGTTTAATTAAGGT[C/T]GGGGAGTATCCAAGT | 11059 |
rs537118554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350441 | AAGCATTTTTGAAGC[A/G]TTTCATGTACACTAA | 11059 |
rs537146705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386684 | TGAAAATATAAACTA[C/G]TTGTAATGACTGTAA | 11059 |
rs537230697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350949 | ATTCTTTACCTTAGA[A/G]GTAAACAAACTAGAT | 11059 |
rs537272899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379235 | TAGAGCAGTTTGGAA[C/T]GATGAAGGATGGAAA | 11059 |
rs537280676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372168 | AGCTGGGACTACAGG[C/T]GCGCGCCACCATGCC | 11059 |
rs537292156 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344473 | TGCATAATTGTGGGA[A/G]GTATTTTGGGAAATA | 11059 |
rs537299328 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373904 | TTTTAATGGGATGGT[A/G]ATAGGCTTGATAATT | 11059 |
rs537356350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86380667 | TTCTTATTGATTGAT[C/T]AGTGTGCAGTACTAC | 11059 |
rs537362905 | in-del | -/TAGAAGCTTA | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86398741 | ATTTGCCACACAGTT[-/TAGAAGCTTA]TGTCTAAGCATGTCA | 11059 |
rs537421906 | in-del | -/T | 0.102726 | 0.202016 | intron-variant | WWP1 | GRCh38.p7 | 8:86412716 | TTTTTTTTGGAATTG[-/T]TTTTTTTTTTTCTCA | 11059 |
rs537464370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407289 | TTCAATCTTTCTTAT[A/G]TCCATTTGTCAACAG | 11059 |
rs537503593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86408124 | TCCTTTCCAGGATGC[C/T]ACATAGTTGGAGTCC | 11059 |
rs537534820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416174 | AATAAGAGCTGTATT[C/G]AAATTGCTGTGAGTT | 11059 |
rs537563368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367750 | TCATATAGTTTTTCT[G/T]TCTTCTCATATCCTG | 11059 |
rs537566037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443042 | CATTTATAGTATGAC[C/T]ACTTTTATTTGTTTA | 11059 |
rs537583943 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349992 | GAGCAACCTGTCCCC[C/G]ACGCGCTCCAAGCCC | 11059 |
rs537584071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409256 | TTTTTTTTCTTCAGA[C/T]GGAGTCTTGCTCTTT | 11059 |
rs537591110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401092 | TAAAATGTTTGATTT[C/T]GTTGTTAGTTATTTA | 11059 |
rs537626230 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422018 | CACCATTCCAAGTTA[A/G]GGCTTCTTGATAAGC | 11059 |
rs537644869 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406563 | CCAGCCTCCTCCAGT[A/G]TTAACATCTTGTATA | 11059 |
rs537670564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401919 | AAAAAAGAAATAACA[A/G]AAAAGAAACTTAAGA | 11059 |
rs537684370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435989 | CAGGCTTGAGCCACT[A/G]CATCTGGCCTGAGTG | 11059 |
rs537689259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449092 | TCATCCTCCTTTCCT[C/T]AGCCTCCCAAAATGC | 11059 |
rs537706987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437575 | ACCCAAAATAGAACT[A/G]TCCATTTAATACTAG | 11059 |
rs537707925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402354 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 11059 |
rs537758180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389312 | CCCTGCGGCCTTCCG[C/T]AGTGTTTGTGTCCCT | 11059 |
rs537765119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445409 | GTCCATGTGTGCCCA[A/G]TGCTGAGCTCCCACC | 11059 |
rs537799316 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390824 | AATAGTCTACCATAT[C/G]AGAATAGATTTTGCA | 11059 |
rs537803964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437737 | AAGCCTTACCAATAA[A/C]GTAAAGAGTCAGTTA | 11059 |
rs537809391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429435 | TACAAGATTATATTC[A/G]TCAAGATGCATATAC | 11059 |
rs537814958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422154 | ATTTGTAACCATCAC[A/T]CAAGTCAAGAAAGAG | 11059 |
rs537836106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395934 | TTTTAAAAGGCTCTT[A/C]TTTAGGAATCTATTC | 11059 |
rs537838643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389904 | CCTCCTGGACGGGGC[A/G]GCTGCCGGGCGGAGA | 11059 |
rs537889501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430538 | CACCTTGCCCTCCCA[A/G]GGTGCTGAGATTACA | 11059 |
rs537928175 | snp | C/T | 1.65061e-05 | 0.00287277 | intron-variant | WWP1 | GRCh38.p7 | 8:86431508 | ATGTATATACAGCAG[C/T]CTTAAGTCGTCTTGC | 11059 |
rs537959826 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363240 | ACTGGTTAATGTCAG[A/G]TTACTTTTTTGTAAG | 11059 |
rs537967630 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391887 | AGGAATGTCTTTCAG[A/G]CCCTTGAGAAAGACA | 11059 |
rs537999385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368375 | TCATCCACTCAGACA[A/G]TGAAGTGGGAAATTT | 11059 |
rs537999987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451734 | GGCTTTCTCTTCATC[A/G]TCTAGAATCTGTGGC | 11059 |
rs538015154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424366 | TCCCAGACGATGGGC[A/G]GCCAGGCAGAGACGC | 11059 |
rs538026804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460263 | CACAAACTATTAAGA[C/G]TGGCAGCAGGGAGGT | 11059 |
rs538060697 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86417594 | AAGTGCTTACTGAAT[A/G]TTTGTTAGATGGTAA | 11059 |
rs538065362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452339 | CTATTTATTTTAAAA[C/G]CATCCTTTTTAATAG | 11059 |
rs538066973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409738 | TGGTGGCGGGTGCCT[A/G]TAATCCCGGCTACTG | 11059 |
rs538067073 | snp | C/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402033 | GGTTGGCTGTTGAAG[C/G]CACGAATGGAATAGA | 11059 |
rs538080370 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341693 | TGAGGAGTTGTAGGC[A/C]GTGGAGAGGGTGAAG | 11059 |
rs538087390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360653 | AGTAACTATTAATTG[C/G]GGGCCTTTCCCCAGC | 11059 |
rs538090816 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86460490 | CTCATAGAATTGTTG[-/T]TGAGAACTAAATCCA | 11059 |
rs538148837 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446620 | CATTTAAGTATTTAA[A/T]CCATCTTGAGTTAAT | 11059 |
rs538177054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361895 | TTTTAAACTCACTGA[C/G]AGCAAAGAGCATATT | 11059 |
rs538188674 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341801 | AAGGAAAACTAGTAA[G/T]TCTGGGTGTGGACGT | 11059 |
rs538192390 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86445954 | CTGCTTATATGTCTT[G/T]TCTTTTCTTTTCTTT | 11059 |
rs538224244 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345707 | TAAGCCACCCTGCCG[G/T]GCCTACTGGGAGCTT | 11059 |
rs538227792 | in-del | -/GAG | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86446823 | GGCTTGAGTTGGAGA[-/GAG]GAGGAGATTTATTTA | 11059 |
rs538240854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86388343 | TACGGTAGCCTCCAA[C/T]TCCTGGACTCAAGCG | 11059 |
rs538311276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390179 | TCCTAGACGGGATGG[C/T]GGCCAGGAAGAGGCG | 11059 |
rs538311832 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86382367 | GGGTTCATAGCTTTT[A/T]TCAGATTCTCAAAAT | 11059 |
rs538344107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382994 | ATCCACATGTAACTT[A/C]AAGATCTGTTTTGAT | 11059 |
rs538368297 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86373446 | CCAATTTGTCAATTT[A/C]TTCCTGTAGTTTTTA | 11059 |
rs538417057 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452990 | TTGCTTCAAAGATCA[C/G]AATTTTAAGTCATGA | 11059 |
rs538444424 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393354 | GCTCTTAGGAATAAC[C/T]CTAGCTACTTAACTG | 11059 |
rs538469964 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415973 | TTGTGCTACATTAAA[C/G/T]GATTTAGAATGACTG | 11059 |
rs538497767 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409062 | ATTCTAAATAAATAA[A/T]CTATTTGTCATTTTC | 11059 |
rs538509728 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424302 | GGCGGCCGGGAAGAG[A/G]CGCTCCTCACTTCCC | 11059 |
rs538524300 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86432602 | ATGTGTTCAATCGCA[A/G]TTCATTTTTTTGTTT | 11059 |
rs538567997 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86463339 | TGAGATGGAGTCTCA[C/G]TCTGTCACCCAGTCT | 11059 |
rs538594793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401880 | AAAAACTCAATTGTT[C/T]GGAAATAGAATCTAA | 11059 |
rs538602457 | snp | A/T | 8.23621e-05 | 0.00641672 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427731 | CGGCCTACCATGGAA[A/T]CTGTCCGAAATTTTG | 11059 |
rs538610527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435871 | GTTTTGTTTTGTTCT[A/G]TTTTCTTAAATAGAG | 11059 |
rs538624426 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449597 | ATTAGGCCCATGGGC[C/T]GTAATTTGCCAGCAC | 11059 |
rs538642596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351791 | GTATTGACCAGTGTT[G/T]GTCAAAGCGCAATCC | 11059 |
rs538686445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86436770 | GAGACGTCTTATTCC[C/T]CCCCTAGTATTATAA | 11059 |
rs538707797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345006 | AAGGATTAGTGGGAT[A/G]GAGGTCTGTAGTGTG | 11059 |
rs538714926 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370246 | TCTTTATACATTTCA[A/G]GGAAAACATTTAAAC | 11059 |
rs538742969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86465803 | AAGTATAAAGGGGAG[A/G]GCAGTATATGGTCTG | 11059 |
rs538777325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374331 | GATGAAGAGAAGATA[C/T]AGCCTCTGTAATGGT | 11059 |
rs538791504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366659 | CCACTAGAAAAGTTT[A/C]TTTGAGATACATCAA | 11059 |
rs538814090 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430459 | CTAATTAAAAAAAAA[A/T]TTTTTTTTATAGAGA | 11059 |
rs538816993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86458670 | AGCAACTTAGTGACT[A/G]GACTTCTGGCTTACT | 11059 |
rs538879200 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392200 | TGAGTTTGCAGTTTT[C/T]CTAGGCCAAGATTGA | 11059 |
rs538892779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375202 | TGTGTGTTTTCCCCC[C/T]TTAGGACGTATAATC | 11059 |
rs538895847 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455582 | AAAGCATCAAAAAAT[A/G]AGCAAATTTAACCAA | 11059 |
rs538955957 | in-del | -/ATAT | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86452061 | ACATGGCCTGTGAAC[-/ATAT]ATATGGTCATTACAT | 11059 |
rs538968619 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467524 | TAAAGTAATGGATAG[A/C]ACCATAACTTACACA | 11059 |
rs538979277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452105 | CTTGCCTTGCTGGTG[C/T]GGAAGGCTTTGAGTC | 11059 |
rs538979837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368546 | CCAGAGCTTCCAAAG[C/T]TATTTTTCCAAAATG | 11059 |
rs539050416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86355877 | GTTAGCTCAGCACTT[C/T]TTATTTTATATTTTG | 11059 |
rs539085650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395091 | GAGCTTGAACTCCTC[C/T]AGTCTACACTCTTGG | 11059 |
rs539086493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361671 | TCTTTCCTTTCCACT[G/T]CTTTCCTTTTGTATG | 11059 |
rs539099178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86389413 | CACATCTTGCACCCC[C/G]CTTAATCCATTTAAC | 11059 |
rs539114947 | in-del | -/CTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382532 | GGTGAAACCTCGCCT[-/CTA]CTAAAAGTACAAAAA | 11059 |
rs539125682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362501 | AGCAACCAAATTGCA[A/G]GGGTAGAAGAATCGG | 11059 |
rs539137442 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86389815 | CCCTCCCAGATGGGG[C/T]GGCTGGCGGGGTGGG | 11059 |
rs539178841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378444 | TTATTGTGAGTGGGA[A/T]TTTTGAGTTAACTCT | 11059 |
rs539234673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354025 | TCCATTAACGTATTG[G/T]CTATTTAGAGCTCGG | 11059 |
rs539267026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382889 | GAGATTCTCTTATTA[A/G]TTCCTAAAAGTAGGT | 11059 |
rs539308363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86424290 | CCTGGACAGGATGGC[A/G]GCCGGGAAGAGGCGC | 11059 |
rs539327223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416895 | GAGACAAAGCCAGAG[A/C]AGCCCCCTTTACCCC | 11059 |
rs539345057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417412 | AAAGTGCATTCTAGA[A/T]AATGCACTTTAGAAA | 11059 |
rs539350334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383885 | AGCATCCTGCACACC[C/T]AAGAAGTCGGTAAAT | 11059 |
rs539373681 | snp | A/G | 0.000399281 | 0.0141238 | splice-acceptor-variant, intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368938 | ATTTATTTGTTTACA[A/G]GGTTGTCTCCTCACA | 11059 |
rs539374105 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341241 | GAAAATCTTAGTACA[C/T]GTTTAAAGCAGAGAT | 11059 |
rs539413272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424796 | AGAGGGAGAGCGTGG[A/G]AAGAGAGGGAGAGGG | 11059 |
rs539413873 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440298 | ATTTTTTATTCCTAA[A/G]TTTTTTATTTAATTC | 11059 |
rs539437879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384611 | GTTGCCTTTGATTCA[A/G]TCTCTTGGTTTAGTA | 11059 |
rs539440111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86376449 | TGGCACATGCCTGTA[A/G]TCCCAGCTACTTGGG | 11059 |
rs539457311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388004 | TTGAGCATTTGAAAT[A/G]TGGTTTGTAGAACTA | 11059 |
rs539478830 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86376949 | ACTTCTGCAATAAAG[A/T]TTACTACTCCTGATT | 11059 |
rs539489981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86403383 | TCACTGCAACTTCTG[C/T]CTCCTGGGTTTAAGA | 11059 |
rs539502419 | snp | C/G | 0.00182769 | 0.0301745 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411679 | AAGAAATACTGACTT[C/G]CTCAGAAAACAATGA | 11059 |
rs539567179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443372 | AGCCACCACTCCCAG[C/T]CTACTTTTCAATAAA | 11059 |
rs539571508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86412629 | TTGTAGCTATTGAAA[C/T]TGCACTTCTAGATGT | 11059 |
rs539601653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371208 | ACCTGTAGTTCATTC[A/G]TTCTCACTACTATAT | 11059 |
rs539666568 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347222 | CGAACTCCTGGACTC[A/G]TGGCCCTCCCACCAT | 11059 |
rs539669096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405086 | CTGATGTCTTTTTGT[A/G]TGATTGTTCATCACT | 11059 |
rs539684147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86390501 | AGCTGGAGACCAGCC[C/T]GTCCAACACGGCGAA | 11059 |
rs539686648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363912 | AATGACAAAAGTAGT[G/T]TACGTGAAACACATT | 11059 |
rs539706130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405875 | TTATGAATTCTGGAA[C/T]ACACCTGGCACTTTG | 11059 |
rs539721616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432480 | TCACCTTTGTGTTGC[A/G]TTATCAGGTTTTATT | 11059 |
rs539806694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432923 | CACAGTTCATTTTTA[C/T]TGCTCCCCTTTACAG | 11059 |
rs539813134 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387861 | ATTTTCTTCCATCTT[C/T]ATAATGAAAAGTTAG | 11059 |
rs539846992 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86359490 | TCTATTCTCATTGAC[C/T]ATTGTATTCCCAGTG | 11059 |
rs539861068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351519 | AGTTTTTTTTTTTTT[G/T]TAGTAGAGATGTTGC | 11059 |
rs539868420 | in-del | -/GTA | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86361061 | GAGTTTGGATTTATT[-/GTA]GTTAAAATGAGAGAA | 11059 |
rs539875858 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415445 | TTTTAGTGCATTTCA[A/G]TGAGTTGCAGACATC | 11059 |
rs539976696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86363488 | TTTTTTTTAACAAAG[C/G]CTACTGAAAGAGGTT | 11059 |
rs540019048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86389615 | CACATTTCCCCCTTT[G/T]CTATTCGACAAAACC | 11059 |
rs540019324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395220 | AGGGAACAAGCCACC[A/C]TAAGCAGAGGTTGTC | 11059 |
rs540065179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456255 | ACCATGAAAGAAAAA[C/T]ATGGATACATTGGAC | 11059 |
rs540080153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355382 | CAGCTCAGCTCCATG[A/G]CTCTGCTTTGTGCTG | 11059 |
rs540101804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430092 | TAGTCCTAGCTACTC[A/G]GTTGTTGCTGAGGTG | 11059 |
rs540103417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389920 | GCTGCCGGGCGGAGA[C/T]GCTCCTCACTTCCCG | 11059 |
rs540116352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86356032 | TTAATGGGACTAATA[A/G]TGATGACTCTAATGG | 11059 |
rs540137931 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441430 | TAACCTTTAGAAAAA[C/T]GTTTATTAACAGGCT | 11059 |
rs540157638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86346699 | TTTCATAATTATTAG[A/G]AAGACTGTTGTTTTT | 11059 |
rs540166212 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360263 | TTTTTGCTTGGTAAG[C/T]CACAGGCTTCAGGTC | 11059 |
rs540175013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398803 | AGCTTTTTAAAAAAT[C/T]ACAGCTTTATTGAGA | 11059 |
rs540209085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424053 | ACTTCCCAGACGGGG[C/T]GGCTGCCGGGCGGAG | 11059 |
rs540264609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444399 | TCTGGCAATGAAAGG[A/T]TATTTAGTTTGGAGA | 11059 |
rs540279853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424387 | GCAGAGACGCTCCTC[A/G]CTTCCCAGACGGGGT | 11059 |
rs540329066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360650 | GTCAGTAACTATTAA[C/T]TGGGGGCCTTTCCCC | 11059 |
rs540347012 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86442215 | TGGATGGGGCAAGTC[-/AT]GTGCATAAAAATGAA | 11059 |
rs540416709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345304 | TTGGTAAAATGCTGG[A/C]CTGGAAAATTTCCAT | 11059 |
rs540454655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446295 | CAGCTGCTTATGTAT[C/G]TTCTTTTGAGAAGTG | 11059 |
rs540459162 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366213 | GGAAGAATAGGACCC[A/T]TCAAGTTCAGGATGG | 11059 |
rs540502709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86454330 | TATTCTTTTTCTCAA[A/G]TATTTTCAATCTACC | 11059 |
rs540508029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430577 | CCACTGCGCCCAACC[C/T]CTTATCATATTTTTA | 11059 |
rs540522562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382425 | GGGTTCTAGCTGGGG[A/G]TGGTGGCTCATGCCT | 11059 |
rs540540498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86439063 | TAAAAAGTTTTAAAG[C/G]CTGGACGTGGTGGCT | 11059 |
rs540595860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86354607 | AATAGTGAATTAACA[C/T]TGTGTATCTATTACA | 11059 |
rs540599834 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420070 | TCTTCTTTCTTAGAA[A/C]GCTACTAGGACTTGT | 11059 |
rs540612338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86397057 | GTCCGGTGATTAGTA[A/G]TTCTAGATTTTTGTC | 11059 |
rs540627047 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467170 | TATCTATATAAACAT[A/G]TATGATAGTGGCTCT | 11059 |
rs540643380 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425731 | AGGCCCAAAACTATG[A/G]TCTACAAAGATTGCC | 11059 |
rs540658776 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347237 | GTGGCCCTCCCACCA[C/T]GGCCTTCCAAAGTGC | 11059 |
rs540664081 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86407739 | TTTAAATTAATAGAC[-/TT]TATATTTTAGAACAG | 11059 |
rs540688009 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467777 | GTAATGTAAACTCTG[C/T]CACTTTTTTGTGTTC | 11059 |
rs540744572 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86369338 | ATTTTATTTGCTGTA[A/T]CTCTTCACTTTTAAG | 11059 |
rs540754196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86433058 | TCTTCACATTGTTAA[C/T]CCAGGCGTTGGTTTG | 11059 |
rs540755639 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86411147 | CAGTTCGTTTGATGT[A/T]AGCTACCACTTACAC | 11059 |
rs540760777 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468613 | GTATGATTTAGCAGA[C/T]TTGACTGAAGAAGGC | 11059 |
rs540779687 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | WWP1 | GRCh38.p7 | 8:86361980 | TGTGTGTGTGTATAT[A/G]TATATATATATACAT | 11059 |
rs540782727 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86369263 | ATGACAGTACCTTAT[A/C]TTTTAAGTGTCATAC | 11059 |
rs540795863 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447536 | CTCCCAAAGTGCTGG[A/G]ATTACAAGTGTGAGC | 11059 |
rs540835158 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86447171 | TAGCATGTTCCATTG[-/C]CCTAGGTACAGGCAT | 11059 |
rs540881600 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WWP1 | GRCh38.p7 | 8:86396549 | ATAAGGTCTTCTTTT[A/T]TCACATGGTTTAAAC | 11059 |
rs540893660 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86462928 | AAGTTCTTTATGAAG[C/T]AGTAAAAATTACTAA | 11059 |
rs540894607 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86346955 | TGGTTCTCATGACAA[C/T]TGATAAGTTGGTGTG | 11059 |
rs540894755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370919 | TGCCCAGGCTGGAGT[A/G]CAGTGGCAAGATCTT | 11059 |
rs540912649 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468592 | ATTGAATATCATTCA[C/T]TGTAGGTATGATTTA | 11059 |
rs540932243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463784 | GTGCAAGACAGGCCA[A/G]GCACGGTGGCTCACA | 11059 |
rs540942502 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86363618 | ACCAGCCTGGCCAAC[A/T]TGGTGAAACCCCGTC | 11059 |
rs540965663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390388 | AGATCACGCCACTGC[A/C]CTCCAGCCTGGGCAA | 11059 |
rs541060472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456455 | ACTTCCCAATAGGAT[A/G]TACACAGATGGCAAG | 11059 |
rs541081117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406128 | TAGCTTCTGACAGGA[A/G]GTAACGTGGTGTCTC | 11059 |
rs541095260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448672 | TGTTGCTTCATTTTC[C/G]CACTGCCATTTGCTG | 11059 |
rs541106992 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86425022 | AAAAAGGGAATAATT[A/C]AGAGGTTAAAAAAGT | 11059 |
rs541115799 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400732 | AACATTTGAAGACTG[-/T]TCAGTATGTTTTTGA | 11059 |
rs541119764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398877 | TTTAGTCGTTTTTAA[C/T]ATATTAAGAGAGTTG | 11059 |
rs541121394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376631 | CTAATTTGAGGTGAA[A/G]AAGAACATACTGAAA | 11059 |
rs541131913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407301 | TATATCCATTTGTCA[A/G]CAGATGTTTATTTTG | 11059 |
rs541135484 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396350 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 11059 |
rs541165383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392020 | ACAACAGACAATAAA[A/T]TCTTTTGGCAGCCTT | 11059 |
rs541223700 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353469 | GAAAGGATTAGTTTG[C/T]ATTTCTTTTTGAGGA | 11059 |
rs541252362 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342315 | TTAAGAAGTCCTGCT[C/T]CGGGATCAGCCGCCG | 11059 |
rs541288000 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351800 | AGTGTTTGTCAAAGC[C/G]CAATCCTTATATAAC | 11059 |
rs541315395 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359353 | ATGAACTATTAAAAT[G/T]AGCTGGAAGAAAAGT | 11059 |
rs541332383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412777 | CACTGCTTAATTACG[A/G]TTTCAGCCTTTGGTC | 11059 |
rs541339976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427155 | GTGACAAGAGCGAAA[C/T]GCCATCTCAAAAAAA | 11059 |
rs541366710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378794 | GGACGTATTTTGGAT[G/T]GATCTGTAATGAACT | 11059 |
rs541368225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355756 | TAAGGAAAGGTATTT[C/T]CAAAGGCTAGCTTAA | 11059 |
rs541416726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86353489 | CTTTTTGAGGAGCCT[A/G]TTGTTTTTTTTTTCT | 11059 |
rs541425575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348377 | GCATGCACCACCACA[C/T]CTGGCTAATTTTGTA | 11059 |
rs541517351 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86432939 | TGCTCCCCTTTACAG[G/T]AAAGCTACTTGCATG | 11059 |
rs541590022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434157 | GTTACTCTCCATACA[A/G]CACAGAGACTGAATT | 11059 |
rs541610977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86375963 | TTCATAATTAGACAC[G/T]GAAGTGGTATCTTAG | 11059 |
rs541635561 | in-del | -/G | 0.00120579 | 0.0245243 | intron-variant | WWP1 | GRCh38.p7 | 8:86400333 | GCAAGACTTCGTCTC[-/G]GGGGGAAAAAAATAA | 11059 |
rs541641194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86383966 | GGAAATTGATTTTCT[C/T]ACATATCCAGAGGCT | 11059 |
rs541651259 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467979 | TCCCCCTTTTTACAC[A/G]GATAATTATTTTTGT | 11059 |
rs541665788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417875 | TGTGCAGCAGGGCAG[A/G]AGAGCTCAAGGCTCT | 11059 |
rs541693557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86369501 | ATAGATTGGGGGTGG[A/G]GATCAGGGTACAGAG | 11059 |
rs541693923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86376510 | GGAGGTGGAGGTTGC[A/G]GTGAGCCGAGATGGC | 11059 |
rs541734892 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377096 | TGTATTGATTTTTTC[G/T]TTTTTTTGAAATGGA | 11059 |
rs541840637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404739 | CCTTGAAATAGGTGG[C/T]AGTATTTTTCCTTTT | 11059 |
rs541854608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86462859 | CTCTATTCTTCAACA[C/T]CATACCCTTGAGGTT | 11059 |
rs541867705 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348604 | TTCTAGGTGCTGGGA[G/T]TACAGTGTTGAGATG | 11059 |
rs541875850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86397270 | AAGTATTTGGCCTCA[A/G]TTTGAATAATAAAGT | 11059 |
rs541877219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412689 | TCAGTCACTATGTTA[A/G]TGTACGTTGGTTTTT | 11059 |
rs541893445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363588 | GGGCCGATCACTTGA[A/G]GTCAGGAGTTCAAGA | 11059 |
rs541929402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374766 | CCTGGCTGGAGTACG[G/T]TGGCGCAAACATACC | 11059 |
rs541929550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86431984 | TTCATAGGTATTAAC[C/T]CATTTTATCTTCCAA | 11059 |
rs541946881 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86362535 | CAAGCTTAGACATCA[-/T]TATTTTAGGAAGTGA | 11059 |
rs541953783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383427 | CACTTCGAAATGAAG[C/T]CCTCACGAATTGTAT | 11059 |
rs542028638 | in-del | -/T | 0.196149 | 0.244131 | intron-variant | WWP1 | GRCh38.p7 | 8:86464520 | GCAGTTGGAAATCCA[-/T]TTTTTTTTTTCCCAA | 11059 |
rs542037661 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462321 | AAAGAGCATGATGTG[A/G]GAGTACGCAGAGAAA | 11059 |
rs542054555 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86424932 | ATAACTTGGAATTCT[G/T]TAAGTAACTTTTTAA | 11059 |
rs542100395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425951 | TTTACTCACACATTC[C/T]ATGTGTACCTGGAAT | 11059 |
rs542108058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86441282 | AGCCTCATCATAGAG[G/T]GAAGTCACTTGGTTC | 11059 |
rs542117074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462243 | AACTAACGGGAACCT[A/G]CTTTGGGTTGGGTGG | 11059 |
rs542139657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412383 | ATTATAATTACTCAA[C/T]TTCCCATGATTTTCT | 11059 |
rs542141104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434000 | CAAGAATTCTAGTTA[C/T]CTCAACTTCAAAACA | 11059 |
rs542185717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426562 | AAACAAAATTCACTC[A/G]TGACACCCTTGGAAC | 11059 |
rs542197649 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86385293 | CTGCAGTGTGTCTGT[-/A]GTTCCTCATCTATTT | 11059 |
rs542224228 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419813 | AGTACATTGGGGCCA[A/C/G]TTAAATTCTAAATAT | 11059 |
rs542225793 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379783 | TAAGTGCCACAGTTA[C/T]GTAATTTCAGAAAGA | 11059 |
rs542243139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354773 | TATATTGTTGTGGAA[G/T]TATGGAAGAAAAATA | 11059 |
rs542260455 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86456229 | AGTTTTTTAGAACAC[-/A]AAAAGCAATAACCAT | 11059 |
rs542276620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447081 | GCAGTAGGGAAATGT[A/G]ATTACCAGGAAACAG | 11059 |
rs542311835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86420519 | GGGTAAGTGTAGATG[A/T]GTATGTGTGCAGGAA | 11059 |
rs542350161 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403857 | GAATAGATACAATTA[C/T]GGTGAAATTAATGAG | 11059 |
rs542362700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447858 | AGTTAGGTTAATTCA[A/G]TTTATAAAACATTTA | 11059 |
rs542366039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464611 | GCCTCAACCTCCTGG[A/G]TTCAAGCAATCCTCC | 11059 |
rs542370728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347323 | ATGCTGAGGCTAAAA[A/G]AAAAGTTTAAAAAGT | 11059 |
rs542371699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440589 | TTTTCCTGAAGTTCA[A/T]TAATTTCACTGTTGA | 11059 |
rs542390792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86414152 | ATGAAATAAAGAAAT[A/G]TAGGCGAGAATAGGA | 11059 |
rs542429218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391293 | CTAATACATTGTCTC[A/G]GAATGTTTGTGGATT | 11059 |
rs542444929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449590 | CCAGATGATTAGGCC[C/T]ATGGGCCGTAATTTG | 11059 |
rs542458576 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86363420 | TTGTCTTGGTCTGGT[A/C/T]TTTTGGGGCCTAGTG | 11059 |
rs542458885 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418024 | AGTGGATGAAGAGGC[A/T]AGAGAGCAGCTATAT | 11059 |
rs542474545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406944 | TACTTTTAGGGTGAG[G/T]ACAAATACGTGGTGC | 11059 |
rs542544542 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367497 | GGATTTGATAGATCT[A/G/T]TAACCTAAGAGTACT | 11059 |
rs542581161 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345568 | GCGCTTGCCACCACA[-/C]CCGGCTAATTTTTGT | 11059 |
rs542582198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86425518 | CTGTCAAGCATTGGC[A/G]TGAGTTACTGAGAGA | 11059 |
rs542583113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349954 | AAGGGTTTCTTGACT[A/G]TCACTCTGGCCTTGA | 11059 |
rs542592021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377462 | TATTGCAGTCTGGCT[C/G]TTTATTGTCTGTAAA | 11059 |
rs542602765 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343557 | TTCGTGTTCTTTTTT[A/T]AAAAAAATTTAATTT | 11059 |
rs542631122 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400857 | TTTCAAAAGATTTGT[G/T]GGCTAACCAGGAGAG | 11059 |
rs542643911 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86377463 | ATTGCAGTCTGGCTG[-/T]TTATTGTCTGTAAAC | 11059 |
rs542676885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463870 | GTTCGAGACCAGCCT[A/G]GGCAACATGGTGAAA | 11059 |
rs542692090 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423014 | AATCAGTATATTATT[C/T]CATAGACACTTTGTG | 11059 |
rs542716799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371713 | TATTCTTATATATGT[A/G]GTTTAAATACTAATC | 11059 |
rs542719646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364284 | TAATAGTTTAGAGTA[A/G]GTGGGTCATAGAATA | 11059 |
rs542720507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387851 | TTTTTATATAATTTT[A/C]TTCCATCTTCATAAT | 11059 |
rs542753635 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WWP1 | GRCh38.p7 | 8:86372311 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTAATT | 11059 |
rs542757189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379806 | CAGAAAGACAAGTTA[A/G]TAGTACCTGGCAGGG | 11059 |
rs542802862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373051 | TATATGTGGTATTTT[C/T]GTTTTTCAGTTCTTA | 11059 |
rs542835537 | in-del | -/AT | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86431219 | ATTCTCTATAATATA[-/AT]ATATGTTATATTCTC | 11059 |
rs542838054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366271 | AGATCAGCAAGATAC[A/G]GGAAGGGTGAGTTGT | 11059 |
rs542843402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365251 | TTTGAAGAAAAATAC[A/G]TTTTTCTCATAGAAA | 11059 |
rs542860210 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396980 | TGATCCTCCTGTGTC[A/G]GCCTCCCAAAGTGCT | 11059 |
rs542898754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400096 | AGTACTTTGGGAGGC[C/T]GAAGCGGGCAGATCA | 11059 |
rs542920642 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86466103 | CCTGAACACCCGAAT[A/C]CTAATCTAGCTACTC | 11059 |
rs542921708 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428363 | GCCATAAGCAAACAT[A/C]CGTGAGAGGAGTGGA | 11059 |
rs542923140 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86449827 | TACTCCGTAGCTTAC[-/T]TTTTTTTTGTCTTAA | 11059 |
rs542925561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367028 | ATCTTTGCCACATTC[A/G]TTGAGTTTTAAATTT | 11059 |
rs542949131 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86372731 | GGGTTTGTCCTTATA[-/TG]CATTGGTCTGTTTTA | 11059 |
rs542959305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458815 | TATTTTAAAGAGATG[A/T]AGACACTTCTAGAAA | 11059 |
rs542968693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433302 | ATTATGCTTTTAAAA[C/T]ATGTGCCTGCTAATG | 11059 |
rs542969118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434677 | CTCCTTCACTAGTAT[A/G]TAAGCTCCACAAAAC | 11059 |
rs542986651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400436 | TTTAAACAGGACAAG[A/T]TGACAGGAATGGAAG | 11059 |
rs542987520 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86387212 | ATATATTAAATGACC[C/G]TTATTTTCACATTCT | 11059 |
rs543033200 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460152 | AACCAGTCAATGAAA[C/T]AGATAATTTTAGAGG | 11059 |
rs543052704 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86348757 | TTTTTCTGGGGTTTG[A/T]ACAAATTATGCAGAA | 11059 |
rs543056668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425737 | AAAACTATGATCTAC[A/G]AAGATTGCCATGAGT | 11059 |
rs543093533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426389 | ATTTATAATTGGTTG[A/C]TGAAAGGAGTTTACA | 11059 |
rs543125805 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86462978 | TTGAGTATATGTTTT[C/T]TTAACATTTGTGTGA | 11059 |
rs543180634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429093 | CTCTGCCATCCATAT[C/G]GCACTTCAGGCCTGT | 11059 |
rs543213721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463826 | AGCACTTTGGAAGGC[C/T]GAGGTGGGAGGATCG | 11059 |
rs543216489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421751 | ATGGTGTGAACCCGG[C/G]AGGCGGAGCTTACAT | 11059 |
rs543247682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371458 | AAAACGCCTACCAGC[A/G]GTGTATAAGAGCCAC | 11059 |
rs543253122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415043 | TATGTACCTCATGCC[A/G]TATACCAAGGAGGCA | 11059 |
rs543365903 | in-del | -/AAAG | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86415546 | TTAGATAAAGATGAC[-/AAAG]AAAGAAAAACACGAG | 11059 |
rs543368537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357424 | AAATCAGTATGAAAA[G/T]TATGATGGTTCATTT | 11059 |
rs543417948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349868 | GACAGCATCCCATGC[A/G]GAAAATGGGCCACAG | 11059 |
rs543467773 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418553 | TGGCCTGTCAGTGGG[A/G]AAAGCTCAGAATATG | 11059 |
rs543480150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442430 | GTAGTTTGGCCACAT[C/T]GAAACTAGCAGGTAA | 11059 |
rs543498710 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428747 | ATGACTTGTACAGAA[A/G]TCTGTGGTAAGGTTC | 11059 |
rs543512461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370960 | AACCTCTGCCTCCCG[A/G]GTTTAAGTAATTCTC | 11059 |
rs543512869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392688 | CTTTAGCCTTATTAA[C/T]TGAGTGAATTTGCTT | 11059 |
rs543513961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377388 | CAGGCTGAGCCACCA[C/T]GCCCAGGCTTTTCTT | 11059 |
rs543521186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343457 | CAACCCCCACCTCCA[C/T]CTTTTGTGACCTGGT | 11059 |
rs543552096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377731 | TTCGATATTTTAGAT[G/T]TTAGACTTTCAACAG | 11059 |
rs543602626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387068 | AATCCCTTCCTAAAG[A/T]CCCTAATTTTTAATA | 11059 |
rs543662615 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86375060 | ATAATATCTGTTTTT[-/A]ATCCTACTACACCAG | 11059 |
rs543678766 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86372406 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTGCCAA | 11059 |
rs543678868 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86379478 | CATCCGGTGTGTATG[A/T]CATGAAAGAGGCTTT | 11059 |
rs543712847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372898 | CTCTTTATTAACTCC[G/T]TTCTTTGGGTTTGTT | 11059 |
rs543736746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86406186 | GTAACCTTGGACAAA[C/T]TGAACATCCTCAAAA | 11059 |
rs543760095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86441605 | TGCCTTCTCATGTGG[A/C]GTCAGTGGGCTGAAT | 11059 |
rs543770054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465467 | GTCTCTACAAAAAAA[A/C]ATACAAAAGTTAGCT | 11059 |
rs543772939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399085 | TGACTGACTTCTTTT[C/T]CTTAGCATGTTTCAA | 11059 |
rs543804602 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342393 | CTTCCCAAATCTCAG[A/C]GGCGGCCCCGCCCCT | 11059 |
rs543811993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407695 | TTGTTGAATTATTGA[A/G]TAGAAATAATTTGTT | 11059 |
rs543834888 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86366619 | AATGAAAAATCTAAC[-/AG]AATTATATTTTTATA | 11059 |
rs543843925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444868 | TTGTATTGCTGATAG[C/T]GATGACTAAGTATCT | 11059 |
rs543860030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86366172 | GGGAAGAGTGCAGTG[A/G]TAGAGATTCCTAGTG | 11059 |
rs543861158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399826 | GTTGGCTGGGGAGGG[G/T]TATACAAATCACAAT | 11059 |
rs543883729 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458794 | TGTTGTGAGTTTATT[C/G]CTTGATATTTTAAAG | 11059 |
rs543900101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408628 | TTTTAAAGTGTTTTC[G/T]TCACGCTGGTTGTGC | 11059 |
rs543900189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400713 | CATATAATAATTTGT[A/G]ATAAACATTTGAAGA | 11059 |
rs543944548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456625 | AAATGAAATGAAATA[C/T]ATATCCACACAAAGA | 11059 |
rs543960359 | in-del | -/A | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468489 | GGGAAACTGGCCTTC[-/A]AAAAAGGACTGCGTA | 11059 |
rs543982158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86387791 | AGCCTCTGAAAGTGC[C/T]GGGATTATAGGCATG | 11059 |
rs543987734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86435182 | TTTCTTTGAAATAGT[C/G]TGTAGTAGACTTTGA | 11059 |
rs544038505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444363 | ACATGGAGATGTAAA[A/G]GAGATAGTTGGAGGT | 11059 |
rs544055832 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454595 | TGGACATCTTGCATC[C/T]TCTAAATTCATACAC | 11059 |
rs544057465 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388357 | ACTCCTGGACTCAAG[C/G]GATCCTCCCACCACA | 11059 |
rs544070884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428018 | ACTTTATAATATTTT[A/G]AAATATTCTAGTTTA | 11059 |
rs544074816 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434824 | AAGAGAACATTTTTC[A/T]TCTGTTCCAAAGTGT | 11059 |
rs544084258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429230 | TGCCTTTTTTACTTA[A/G]CGAAGGATGCCCTCA | 11059 |
rs544117505 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415923 | ATGCCTACCGTATAG[C/T]AGGCACTCAATAAAT | 11059 |
rs544124052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436214 | TTACTAAAATAAAGC[C/T]TAAACAGCTTTTGGA | 11059 |
rs544136148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389032 | GCTTTGATAACTTGC[C/T]TAAAGTTAGAAACCC | 11059 |
rs544170748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430005 | GGAGTTCGAGACCAG[C/T]CTCAGAAACATGGCA | 11059 |
rs544199657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415577 | GAGTCTTGAATGTAC[C/T]ATTATGATGAATTTT | 11059 |
rs544206946 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86423635 | TTCTTTCTACACAGA[C/T]ACAGCAACAATCTGA | 11059 |
rs544224622 | snp | A/G | 3.35267e-05 | 0.00409417 | intron-variant | WWP1 | GRCh38.p7 | 8:86458050 | TTTATCTTTTTTGAA[A/G]CAAAGTACTCAACAT | 11059 |
rs544262070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450376 | AAAAAAACAGTAACA[C/G]TATATTTTGAGGAAA | 11059 |
rs544278919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424045 | CGCTCCTCACTTCCC[A/C]GACGGGGCGGCTGCC | 11059 |
rs544314340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359373 | GGAAGAAAAGTCTTG[A/C]CTATGGGGATTGGTG | 11059 |
rs544333050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466699 | TATATAGTATACATA[C/T]ATCCATTCAGCATTT | 11059 |
rs544340967 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441259 | TTACCTGGGGTATGT[A/C]TTACTTCAGCCTCAT | 11059 |
rs544345996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86451000 | GTGGATCACTTGAGC[C/T]CAGGAGTTCAAGACC | 11059 |
rs544386871 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360877 | TTCTGAAGAGATCAT[A/G]TATAAGTTGAGTTCT | 11059 |
rs544387662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367976 | ACCGTGACTCCCAAA[C/T]GTTTCTTCTCCATGG | 11059 |
rs544414964 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390832 | ACCATATCAGAATAG[A/G]TTTTGCAGTTATTGA | 11059 |
rs544438689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452796 | CACAATCTTGAATCC[A/T]CTCATTTGTCCTGAT | 11059 |
rs544447647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409573 | TAATAGAAGTTCTTA[A/C]AATAGGCTGGGCACA | 11059 |
rs544452195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394528 | ACAAAAACATTCTTT[C/T]AGTGGTAAGTGCATT | 11059 |
rs544487119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345111 | GTGGTGCACGCGAAT[A/G]GAAAGGAAGAAAGGA | 11059 |
rs544489439 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347298 | GCCAATCATTGCTTT[A/T]TGGATGAATATGCTG | 11059 |
rs544526573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453460 | TTGAGGGACCTTTGT[A/G]TGGCTTCCATCTTTT | 11059 |
rs544532843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86352739 | CTGAACCTTCCAGAT[A/G]TTTAAAACAGCCTAA | 11059 |
rs544539741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389488 | GTAAGGTTATAGATT[A/T]ACAGCATCCCAAGGC | 11059 |
rs544654153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419448 | ACAGACTATTTTAAT[A/G]TCCTCTGAGGGATAA | 11059 |
rs544704352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407035 | AGTTAGGAAGCTATG[C/T]CTTGTAACCCAGAAG | 11059 |
rs544707617 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467118 | GATCATCCTTAAATT[C/T]TGAAGCAAGTGAGAG | 11059 |
rs544726268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375370 | AGTCAAAACCAAGGT[A/C]CATTTAGAGAGGTCT | 11059 |
rs544782029 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457982 | GAAATACTGTTTATC[A/G]ACATTATACAAGAAA | 11059 |
rs544787848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368562 | TATTTTTCCAAAATG[C/T]AATTCTCATCACTGA | 11059 |
rs544792351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365640 | GATCAATCAGTGATA[C/T]AGGGAGAGGTCAAGT | 11059 |
rs544831686 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420817 | AAACTATCTGAAAGT[A/G]TATGTAATTTTGATA | 11059 |
rs544916341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435299 | CCCCATTACTTGAGC[A/T]TCTTTTGGCCCACCA | 11059 |
rs544953750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86403585 | CAGGCGTGAGCCACC[A/G]TGCCTGGACAGTAAT | 11059 |
rs544965057 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388884 | TTTAATTTTATATTC[C/G]CATTTGCTAACAGCC | 11059 |
rs544987330 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390513 | GCCCGTCCAACACGG[C/T]GAAACCCCGTCTCCA | 11059 |
rs545015955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372808 | CAGACATTTATTTAT[C/T]TTAGTGTTTTCTAAG | 11059 |
rs545040970 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400320 | TCTGGGCGACAGAGC[A/G]AGACTTCGTCTCGGG | 11059 |
rs545052598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457437 | TCTGTCTGTCTATCT[A/G]TCTATCTATCTATCT | 11059 |
rs545103588 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372521 | AGAGGACACAAAACA[A/T]TAGTTTTCTGCTGTA | 11059 |
rs545136904 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445344 | CTTGCCTTCCTCCCT[C/T]TCTCCCTCCCATCGT | 11059 |
rs545140634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366106 | ACAGTGAAGGGATGC[C/G]GGAGAGTGCTGGAGA | 11059 |
rs545149678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422485 | GTGCATCAGCATACC[A/G]AGTAGCTTGGATTAC | 11059 |
rs545165555 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451462 | TAAGGTGTACTCTTA[C/T]AATGAGTGTGGTGGT | 11059 |
rs545176003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86373871 | TTTTCTGTTATTTCA[A/G]CTAACTTTAGGGTTT | 11059 |
rs545177607 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86358344 | ATGTAAAATTTCAGT[A/T]CTATGCTATATAGGT | 11059 |
rs545195443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466683 | TGGCAAAATTTTAAC[A/G]TATATAGTATACATA | 11059 |
rs545219430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450929 | ATGTCTTAAAAGATG[C/G]ATGAGAGGCTGGTGG | 11059 |
rs545238225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401271 | TTAATAAAGTTATAA[G/T]AGTTTCAGGCCAGGT | 11059 |
rs545260668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351225 | TGCTCGTAATTCAGT[A/T]TTATGAAGTTGAAAA | 11059 |
rs545299621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460477 | ATGATTCTACCTATC[C/T]CATAGAATTGTTGTG | 11059 |
rs545311757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360230 | CAAAATCATCTGAAA[A/G]TAAGTTTCTGGTGGT | 11059 |
rs545362177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388041 | TTAATTTTAAACTTG[A/G]TTTTATTTTAATTAA | 11059 |
rs545398251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388876 | AGTTGCTTTTTAATT[C/T]TATATTCCCATTTGC | 11059 |
rs545407177 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390954 | TATCTTTTCTGATAT[A/T]TTTGGGGTAATGGTG | 11059 |
rs545461467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429891 | GATAGTCTCCTCTTC[A/G]TGACATTTTATGAAC | 11059 |
rs545471765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445104 | GAAGTGCCATACTCT[C/T]TTTAAAACCAGCTCT | 11059 |
rs545485029 | snp | A/G | 1.65916e-05 | 0.00288019 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380814 | AGAAATTACGAAAAC[A/G]GCAAAATCCAGTAGT | 11059 |
rs545491740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345403 | TCATCTCAGAATTTC[G/T]TGGAGCTTTTTTTAT | 11059 |
rs545541409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86389944 | CTTCCCGGACGGGGC[A/G]GCTGCCAGGCGGAGG | 11059 |
rs545578194 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86382621 | GGAGAATCGCTTGAA[A/C]CCGGGAGGTGGAGGT | 11059 |
rs545582968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415719 | AGATTAATTTTCCCT[G/T]CTGTAGAACTTACTA | 11059 |
rs545611974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367908 | TTATTCCAAAATATC[C/T]CCACTGTGAACAAGC | 11059 |
rs545658268 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86383299 | CATATTCCCATTGTT[A/G]GACATCTAGATTGTT | 11059 |
rs545694554 | in-del | -/AG | 0.00119784 | 0.0244435 | intron-variant | WWP1 | GRCh38.p7 | 8:86414301 | CAATCTGGTATACAC[-/AG]AGATATTTATATAAA | 11059 |
rs545722669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86424134 | CTTCTCAGATGGGGC[A/G]GCCGGGCAGAGACAC | 11059 |
rs545737170 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86436500 | CTTTTTCATAACCAC[C/G]CAACATAGTGTATTT | 11059 |
rs545752703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410092 | TCAAATCATCCTTGA[A/G]TTTATACATGATGTT | 11059 |
rs545773497 | snp | C/T | 6.62153e-05 | 0.00575354 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452575 | TTAATGACAGAATGG[C/T]GTTTTTCTCGAGGAG | 11059 |
rs545795131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86411240 | TCAGAATTGATGATT[C/T]GGAGGGAAAACACTG | 11059 |
rs545876452 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468475 | AGGTTATGTGATAGA[C/G]GGAAACTGGCCTTCA | 11059 |
rs545879896 | in-del | -/TTG | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86408955 | GGTCTTGAAGTAATC[-/TTG]TTGTTGATCTTGTGT | 11059 |
rs545880430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418278 | CAAACTTTGTGGAGC[A/G]TATGGTCTAATATAT | 11059 |
rs545883136 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412157 | TTATTTCTACTTTTC[A/G/T]TAAGAGTGACCATGA | 11059 |
rs545955093 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408126 | CTTTCCAGGATGCTA[C/T]ATAGTTGGAGTCCTA | 11059 |
rs546026542 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439086 | TGGTGGCTTACGCCT[A/G]TAATCCCAGCACTTT | 11059 |
rs546054957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86424406 | CCCAGACGGGGTGGC[A/G]GCCGGGCAGAGGCTG | 11059 |
rs546058621 | snp | A/C/G | 0.000198726 | 0.00996624 | intron-variant | WWP1 | GRCh38.p7 | 8:86431791 | TTGCTTAGTGAGCAC[A/C/G]TGAGATTTAGTCTCT | 11059 |
rs546105880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86447817 | GCCTTTTCAGGTGCA[C/T]AGGGCCCTTTTATAT | 11059 |
rs546142522 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86397932 | TAATTAAGAAACCAA[A/G]GCTTAAAGATGTTTG | 11059 |
rs546194575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461464 | AAAGAAAAATGAGTG[C/G]CTAATATCAAAGCAC | 11059 |
rs546203062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393503 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 11059 |
rs546218392 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436870 | GGAGTAATGATACTC[-/T]TGAGCCCCAAGAGAA | 11059 |
rs546249987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362089 | ACATATATACACACA[C/T]ATATATATACACTAG | 11059 |
rs546319428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454446 | GACTGTCACTAATCC[C/T]GGTTACCATCTTCCT | 11059 |
rs546335406 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380453 | ATTGATTGTGGTGAT[C/G]GTTGTGCCACTCTGA | 11059 |
rs546351803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353705 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAAGT | 11059 |
rs546367526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447052 | TAGTCATCTAGGAAA[C/G]TGGGAGAGTGAATGC | 11059 |
rs546370678 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462900 | AAAAAAAAAGAAAAA[G/T]GCAAGTTCGTTGAAG | 11059 |
rs546374436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354695 | TATTCCTTTCAAGTT[C/T]TTAAATGTAATTTCT | 11059 |
rs546385653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347256 | CTTCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 11059 |
rs546399954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397202 | GACTTCATCAAAAAC[A/G]TGAAATGTTCCATGA | 11059 |
rs546439163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86422738 | TAAAGAGAAATTAAC[A/G]GGAATCACAGAAGAA | 11059 |
rs546448924 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340992 | AAGGCTGGTTCAATA[C/T]TGGGTGTCAGCTTGA | 11059 |
rs546488670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86445558 | GCTTACAGTCCACCA[C/T]TGATGGGCACCTGGA | 11059 |
rs546490870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347746 | TGAATTTAATTCTGT[A/T]GCTTTTACAGATGAA | 11059 |
rs546592758 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86425997 | TCAGATTTCCCTTCC[-/AG]ATTCAATTTAAAGCC | 11059 |
rs546640796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409036 | GGGTTTTTAAAAAAA[C/T]TTTCTTGTGTATTCT | 11059 |
rs546669048 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86359765 | ATCATTAAAAACAGT[C/T]CTCGGCGGGCGCAGT | 11059 |
rs546679434 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86401848 | ACTCTATTTACCTAT[C/G]ATTTTACTTGAAACA | 11059 |
rs546694861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445352 | CCTCCCTCTCTCCCT[C/T]CCATCGTAGTCCCCA | 11059 |
rs546698167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436298 | AGTTTTGATAATGCT[A/G]TCAAATTAAAATTAA | 11059 |
rs546700053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86351700 | TTAACATGGCTGGCA[A/G]TATATCAGCTAGTGA | 11059 |
rs546743881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344801 | TTTGGGGAAAGGCAG[G/T]TAATTATGTTTGGGT | 11059 |
rs546748717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381106 | CTGTTTTGGTACAGA[A/T]ATAAATAGGACTGCA | 11059 |
rs546776491 | in-del | -/CTTTTT | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86383130 | ATATTTGGCTTAAAA[-/CTTTTT]CTTTTTCTTAAAGCA | 11059 |
rs546806286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402970 | GAAAGTTTATTTTCC[A/G]AAAGTAAGCATTACT | 11059 |
rs546819124 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | WWP1 | GRCh38.p7 | 8:86437994 | TTTAGTAGAGACGGG[C/G]TTTCACCATGTTAGC | 11059 |
rs546904301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430457 | GGCTAATTAAAAAAA[A/T]ATTTTTTTTTATAGA | 11059 |
rs546932889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382214 | CTAGAAATTTAACAA[C/T]ATACCATAAATATTA | 11059 |
rs546948516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466720 | TTCAGCATTTCTATG[G/T]GCTTTGAAAAGTATT | 11059 |
rs546983149 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422737 | CTAAAGAGAAATTAA[C/T]GGGAATCACAGAAGA | 11059 |
rs546989791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464919 | TACACACATGCGCGC[A/G]CGTGTGTGTGTGTAT | 11059 |
rs547007833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368120 | CCCACAATAAAAACA[A/G]TAAGTCATCTTTATT | 11059 |
rs547031088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86432125 | ACGATGACAGTCAGT[C/G]TCTGTCTAGACTCTG | 11059 |
rs547037595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451991 | TCCAATAAAACAGCA[C/G]GTAAAGAACCTGTTC | 11059 |
rs547044644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360479 | CAGACTGTTAGTCCT[C/G]GGGTTACCTAGGTTC | 11059 |
rs547053540 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86383469 | TACCTTGGCTGTGTG[A/C]AGTGGTTCATGCCTG | 11059 |
rs547059981 | snp | A/G | 0.000120131 | 0.00774928 | intron-variant | WWP1 | GRCh38.p7 | 8:86402216 | CTGGTAAGCAAGGCT[A/G]TTTATGACACCTTGT | 11059 |
rs547060922 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468049 | GCTGAACTACAAAAA[A/T]GTGTAACAAATTAAA | 11059 |
rs547107299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86352286 | TTGGAGTGCAGTGGC[A/G]CTATCTCGGCTCACT | 11059 |
rs547116886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424579 | AGGCTGAGGCTGGCA[G/T]ATCACTCGCCGTTAG | 11059 |
rs547131036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86461044 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTGCTT | 11059 |
rs547140117 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386949 | CTGAAGGGGATGAAC[A/T]CTGTCCTCACATGGC | 11059 |
rs547144417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394843 | AATATATACTGTAAA[C/T]ACCCTCCCACTGCAG | 11059 |
rs547145477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376119 | TGAAGAACCACTTAC[A/G]TAATTCCTTCTACTT | 11059 |
rs547151435 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86421580 | CTGTAATCTCAGCAC[C/T]TTGGGAGGCCGAGGC | 11059 |
rs547168693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345498 | CATTGCAACCTCCGC[C/T]TCCCAGGCTCAAGAG | 11059 |
rs547187349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86416988 | CCACATTCTGGGGAC[G/T]CACTTTTGGTAGCTA | 11059 |
rs547195915 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461410 | TGATTGAACCTAAAG[A/G]TTACTCTTCTGTGCT | 11059 |
rs547216575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86363034 | TCATAAAGTGCTTAT[A/G]TAATCTTACCTTGAA | 11059 |
rs547228378 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86395745 | AAAAATTTATGAATT[A/G]GAATTGCAGAATTAG | 11059 |
rs547266967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390095 | TCCTCACATCCCAGA[C/T]GGAGCGGCGGGGCAG | 11059 |
rs547286107 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86430965 | AGAATGTTATATATT[C/G]TGTATACTATATAGA | 11059 |
rs547322686 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86424218 | GACGGGGCGGCGGGG[C/T]AGAGGCGCTCCCCAC | 11059 |
rs547340879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454778 | GGCAGGGTTTATAAT[A/G]TTCTCACATACTGCC | 11059 |
rs547350857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375666 | TAAAAAAGCTAACTA[A/G]TCTCCTTTTGCTGGA | 11059 |
rs547363574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404863 | CTTTGCCTTCTTCCT[A/G]TTCATTTTGATGTGT | 11059 |
rs547401036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86397643 | AGTCTAATATATAGA[A/C]GTCTAATATATCGTT | 11059 |
rs547417409 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361160 | ATCTAGGTTGGGAGT[A/G]AAGAGTGGGGCAGGA | 11059 |
rs547438558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391415 | GCGGAGATGTGTGGT[A/G]TTTTTAGCTTTCTTT | 11059 |
rs547481163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86453308 | ACTTTCTGTGACTGG[A/G]TTATTTCACTCAGCC | 11059 |
rs547509949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461603 | ATGATCTAATTCTTA[C/T]TGCTGGATCTCTGCA | 11059 |
rs547537064 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341367 | TGTCAGGAGAGCTCC[A/G]AAAAGCCAAAGAATG | 11059 |
rs547577343 | snp | C/T | 5.32288e-05 | 0.00515864 | intron-variant | WWP1 | GRCh38.p7 | 8:86411520 | TGATAGATGATTTTA[C/T]TAATTTTCCCTTCTC | 11059 |
rs547579366 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429545 | TCAGAATATATTTCT[A/G]GGTTATAAGAATGGA | 11059 |
rs547586887 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370575 | AGGATCCACAGTACC[A/C]CACATTTCTGGATTT | 11059 |
rs547590809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354013 | TGATTTAATTTTTCC[A/T]TTAACGTATTGGCTA | 11059 |
rs547624438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412414 | TTAAAGAGTATTCTA[G/T]ATGTGTATTCCATTC | 11059 |
rs547654824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377531 | TTTTAGCATATTTAC[C/T]CTTATCCTCATTTCT | 11059 |
rs547661232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413074 | CCTCATGATCCACCC[A/G]CCTTGCTTCCCAAAG | 11059 |
rs547668397 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86396820 | GGCCAGGTTGGTCTT[A/G]AACTCCTGGGCTCAA | 11059 |
rs547679285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446579 | TCCTAGGTTTTCTTT[A/T]AGGATTTTAATAGTT | 11059 |
rs547704732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347217 | GGCCTCGAACTCCTG[A/G]ACTCGTGGCCCTCCC | 11059 |
rs547704927 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454596 | GGACATCTTGCATCC[C/T]CTAAATTCATACACC | 11059 |
rs547719306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447381 | AAGCAATTCTCCTGC[C/T]TCATCTTCCTGAATA | 11059 |
rs547782401 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86458326 | TAGTCTAAATTCCAC[-/T]TTAATTCTAGAAGTA | 11059 |
rs547784877 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86356010 | TCAACCTAATTTTTC[A/T]TATCTGTTAATGGGA | 11059 |
rs547795452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86432888 | GCTGGGATTACAGGC[A/G]TGAGCCATCACACCC | 11059 |
rs547806191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440025 | TCCTCATTTACAACA[A/T]CATTAAACTTTTCCA | 11059 |
rs547841958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440682 | CTATTATGTCTTTGA[A/G]TATTTTTTCTGTTCC | 11059 |
rs547856883 | in-del | -/TATT | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86393208 | TTATTTTTTAATTTG[-/TATT]TATTTATTTTTTTGA | 11059 |
rs547880368 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397869 | TATGGTTTTGCATTT[G/T]GTCCTCAACACTGTC | 11059 |
rs547882511 | snp | A/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425241 | GGAACAAAGAAAAGA[A/T]CCTCATGGTAGAACC | 11059 |
rs547928513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375584 | TAACTTTACAGTATT[A/T]TTCTGGAGTTTGTTT | 11059 |
rs547969233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368725 | GTCCACTATGCAAGC[A/G]GTTCTCTGGATGTGC | 11059 |
rs548017203 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376938 | ATCTCACAATAACTT[C/T]TGCAATAAAGATTAC | 11059 |
rs548045256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419985 | CTGTATCCAGCCACA[C/T]TGTTTAGTGTTTGCA | 11059 |
rs548060917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463112 | TTCTTTTATGGAACA[A/C]TATTTTTACTTGAAA | 11059 |
rs548061738 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373751 | GGTATGGGAATCTCA[C/T]TCCTTCCCCTTGTAG | 11059 |
rs548067652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86464530 | AATCCATTTTTTTTT[C/T]CCCAAGATAGAGTCT | 11059 |
rs548071945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86403192 | TTTTTATTCAAGAGC[A/G]TATGTTCCTCCCTGT | 11059 |
rs548090855 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | WWP1 | GRCh38.p7 | 8:86418247 | AGTATACTGATTTGC[-/A]AAACAGTTGAAGGCC | 11059 |
rs548109644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403807 | TAGGTAGAATTTTTT[A/C]GTCTTAATTTAAGGT | 11059 |
rs548115010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363826 | AAAAGAAATTTGTCT[A/G]TGGTCTTGCTGATTT | 11059 |
rs548137889 | in-del | -/ACAC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457547 | GTATACATAATAGAT[-/ACAC]ACACACATTTAGATA | 11059 |
rs548166778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430423 | GTAGCTGGGACTTTA[A/G]GCATGTGCCAACACA | 11059 |
rs548175375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86427104 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCAC | 11059 |
rs548190154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382072 | TTATAGAGTAATATA[A/C]AAATTTTCTATAATT | 11059 |
rs548196529 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86396774 | AATTTTTAATTTTTT[A/T]AAAAAAATAGAGACA | 11059 |
rs548197867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362235 | AAAAATTGTTAAAAT[A/G]CCTAATGCCTAGTTT | 11059 |
rs548240324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353906 | GATGTTTACAAGTGA[A/G]TACCGAACAGAACGT | 11059 |
rs548253714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86423847 | CGGGGCGGCGGCTGG[A/G]CAGAGGCGCCCCCCA | 11059 |
rs548385386 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401119 | TTTATTTGCTGATGT[A/G]TATACTATACATTTT | 11059 |
rs548408811 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348240 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCCCTCTTG | 11059 |
rs548412832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439764 | CCTTATTTGTTCTGC[C/T]CCAGCCTAATTTGGC | 11059 |
rs548448587 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398694 | GAACATATTTCCTGA[A/G]TAAGAAGTTTTATAT | 11059 |
rs548456270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432710 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 11059 |
rs548472811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453150 | ATCCAATCTCCAGAA[A/T]TTTTTCATCCTGCAA | 11059 |
rs548512533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445975 | TCTTTTCTTTTCTTT[C/T]CTTTTTTTTTTTTTT | 11059 |
rs548512633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453818 | ATGATTAGTTATCAA[G/T]AATTTTCTAAAGCTT | 11059 |
rs548517464 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86355843 | ATTGATACAGCAAAC[-/TT]CTCATTTTAAGGCAT | 11059 |
rs548541889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419373 | CAGTGAGCTGAGATC[A/T]CACCACTGCAGTCCA | 11059 |
rs548596568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439203 | AAAAAATTAGCCAGG[C/T]GTGGTGGTGGGCGCC | 11059 |
rs548597181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446472 | TTGCTGTGCAGAAGC[A/T]CTTTAGTTTAATTAG | 11059 |
rs548597653 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461378 | GATAATAATGGCCTT[G/T]GGACATACAATAGAC | 11059 |
rs548617256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390460 | CACTTCGGGAGGCCC[A/G]GGCTGGCAGATCACT | 11059 |
rs548617759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347107 | CCTAGACCTCAGCCT[C/T]CCAAGTACTTGGGAC | 11059 |
rs548638483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455960 | AAGTAGATCCACACC[C/T]ACATTGTCAATTGAT | 11059 |
rs548705185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383671 | TGCTTGAACTGGGAG[A/G]CGGAGGTTGCAGTGA | 11059 |
rs548711819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86413009 | AATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 11059 |
rs548763001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448886 | TGTCGCTCAGGCCGT[C/T]GTAGTGGCGTGATCA | 11059 |
rs548776295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376349 | CGAGGCAGGTGGATC[A/C]CGTGAGGCCAGGAGT | 11059 |
rs548780625 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86349356 | TTAGACTTGTAAGGG[A/T]TACAGTATCATTTCT | 11059 |
rs548790757 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341105 | GAGGAGGCCTGCATG[C/T]ATTCTGGAGAAGGAG | 11059 |
rs548795870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405678 | TTGGGACTATAGGCA[C/T]GTGCCACCATGCCTG | 11059 |
rs548797497 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463062 | AAGGAAAGCTTTTGG[A/G]CAGTTGTTTGAGTTG | 11059 |
rs548814399 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389302 | AGGCAGAGGACCCTG[C/T]GGCCTTCCGCAGTGT | 11059 |
rs548816648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86355905 | TTGTTTCTGCAGTGC[A/G]TATGTAGTGAAAAGA | 11059 |
rs548873948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86448884 | TCTGTCGCTCAGGCC[A/G]TCGTAGTGGCGTGAT | 11059 |
rs548891205 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342413 | GCCCCGCCCCTTCCA[A/C]ACGTTCAGGCCCCGC | 11059 |
rs548936127 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86393000 | GCCACATTATTAGAT[-/A]AAAAAAATGAGAAGT | 11059 |
rs548936380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412546 | TGTACAGTATATACA[A/G]TACAGTCAGAAAGTA | 11059 |
rs548965367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404970 | TTTCACCACCTCTGA[C/T]TATTGCTAGTGACAT | 11059 |
rs548997625 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391587 | GAACATACTTTAATC[A/C]ATAATATGTTTTTGC | 11059 |
rs549049708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386379 | GTGTCTGTGTACAGT[G/T]GCTGTACCCTAGCCT | 11059 |
rs549068724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372496 | TCTCTTAAGAAATCC[C/T]TCCATCCTGAGAGGA | 11059 |
rs549071836 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359974 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 11059 |
rs549083723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378184 | TTTATTTGAATATTT[A/G]AGTCTCCCTTCCTTT | 11059 |
rs549126978 | in-del | -/GT/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414248 | TGTGTGTGTGTGTGT[-/GT/TA]ATGTGTGTGTATGTA | 11059 |
rs549127870 | snp | A/G | 3.29815e-05 | 0.00406075 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398446 | TTGGTGATTGAGCAA[A/G]AAAATATAACAAACT | 11059 |
rs549152936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365679 | GAAAGCTTTAATTTT[C/T]TGGCGGGTCACAGTG | 11059 |
rs549157703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86440903 | ATTTTTCTTCATTAG[C/T]GGTTTTACTGTTTTC | 11059 |
rs549194755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86433778 | GTAAAATTAGCTGGG[C/T]GTGATGGCGTGTGCC | 11059 |
rs549215807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391750 | AAATTACAAAAGCTT[C/G]GTCAGTGTAAATGCA | 11059 |
rs549253400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464920 | ACACACATGCGCGCG[C/T]GTGTGTGTGTGTATT | 11059 |
rs549284195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414383 | AATCCAGGGGAGAAA[A/T]TAAGAGAGCCTGAAG | 11059 |
rs549314498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407164 | CTTCTGCTATCATAA[C/G]TATTACATAAGATTT | 11059 |
rs549337331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357952 | CATTTGTCACAATGT[G/T]TCTGTGGGAAAATTT | 11059 |
rs549340375 | in-del | -/A | 0.474588 | 0.10982 | intron-variant | WWP1 | GRCh38.p7 | 8:86442844 | AGAGAAGGCTTTTAA[-/A]AAAAAAAAAAAGGAT | 11059 |
rs549351259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461647 | TCAGGCAGAAGCAGC[G/T]TACATTGTGAATTTC | 11059 |
rs549358508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426959 | TGAGGTCAGGAGTTC[A/G]AGACCATCCTGGCCA | 11059 |
rs549380002 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351505 | AACATGCTCAGCTAG[-/T]TTTTTTTTTTTTTTT | 11059 |
rs549407213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427314 | ATGATGTGTTGATAG[C/T]TGCAGCAAACGACCA | 11059 |
rs549421717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86379072 | ACACCATCATATACT[C/G]ACTTTTCCTTCTTCC | 11059 |
rs549440193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462509 | CGTTATAGGCTAATT[A/G]AAGAACTGAGATGTC | 11059 |
rs549443792 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86413834 | CATTAAAGAATGTAA[A/G]GCAGGGGAGTGGCAT | 11059 |
rs549447229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350272 | GCAGTATTTTTTGTT[C/T]GTTTGTTTTTAGTTC | 11059 |
rs549465346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86425092 | TAATAGCCTTTATAT[A/G]TATAGCTGTGTGTGT | 11059 |
rs549484277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421209 | ACAGTACTGAATATC[A/G]TGAGTGTTCCAGTGT | 11059 |
rs549500250 | snp | C/T | 0.000188768 | 0.00971332 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468641 | GGCAGCTTTCCAGTT[C/T]GTTTTCAGGGTGCTG | 11059 |
rs549560918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355067 | CATGTAGGTCTGTCC[A/G]ACTTGAAAACTGTTC | 11059 |
rs549565099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86455681 | ATGAAGAGATATACG[A/G]TGTTATATTGTTAAA | 11059 |
rs549583399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347596 | TCACTGCAGTGGCTA[C/T]TGGTAGGTGATATTT | 11059 |
rs549583787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370271 | TTAAACATCATAAAA[G/T]ATGTTTGAGCAGACA | 11059 |
rs549593808 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86459224 | CATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 11059 |
rs549674117 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424289 | TCCTGGACAGGATGG[C/G]GGCCGGGAAGAGGCG | 11059 |
rs549703116 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | WWP1 | GRCh38.p7 | 8:86442838 | TGTATTAGAGAAGGC[A/T]TTTAAAAAAAAAAAA | 11059 |
rs549703139 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86450498 | ACAATCTAAGTGGTT[A/T]AAAAAAATGCTATCA | 11059 |
rs549740814 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369906 | TACATTCTTTAAATT[-/A]AAAAAAAAAACCCAT | 11059 |
rs549745794 | in-del | -/TTAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451934 | TGTTTTGTTTTCATC[-/TTAA]TTGAGTTCTTCTATT | 11059 |
rs549785674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376690 | CCAGTTGGAAAATAG[A/T]TGTGGACCAAGGCAG | 11059 |
rs549800765 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367990 | ATGTTTCTTCTCCAT[G/T]GACCTGTTTCCTCAA | 11059 |
rs549829740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86440819 | TTTCCATTTTATTTT[C/G]ATTTTTCTCAAGCCT | 11059 |
rs549839932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391604 | TAATATGTTTTTGCA[A/G]TAAGGAAGAGATTCC | 11059 |
rs549854532 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403364 | GCAGTGGCAGGATTT[C/T]GGCTCACTGCAACTT | 11059 |
rs549863502 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363873 | ATTCTGTGCCAGGAA[A/G]TATTTTTAGTGCTTT | 11059 |
rs549946615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447412 | GCTGGGACTACAGGC[A/G]CGTGCCACCATGCCC | 11059 |
rs549957133 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86397661 | CTAATATATCGTTTA[A/T]TGCATAGTCTAAATA | 11059 |
rs549986607 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346184 | TGAGGGATGAATTGG[C/G]TAGAGAAGAGCAGTT | 11059 |
rs550016959 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347417 | TTTGTTCCTATGTCA[A/G]TATTCTTTTCCCACC | 11059 |
rs550018957 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348977 | AGTTGCTGGCCTTAC[C/T]TGGTAGCTGATGGCT | 11059 |
rs550062679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420253 | AAGGCAGGTGCAATC[A/G]TAGAACAGCTAATGA | 11059 |
rs550089382 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86371845 | TCAAAATATTCACCC[G/T]TTTTTTCTTTTTTTG | 11059 |
rs550093156 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456184 | GAATGTGAAAGTGAA[A/G]AACATAAGAGAAATC | 11059 |
rs550141633 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86381757 | TATTGCTTGTGATTG[A/T]TTAACTTTGTGGCAT | 11059 |
rs550167955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400148 | AGCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 11059 |
rs550177953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86364704 | TCAACTACTTGAGAG[C/T]CTCAGGCAGGAGGAT | 11059 |
rs550243788 | in-del | -/TATA | 0.00517822 | 0.0506191 | intron-variant | WWP1 | GRCh38.p7 | 8:86457572 | ATTTAGATATAAATC[-/TATA]TATATAGATGTGTGT | 11059 |
rs550244738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426117 | ACTCAGGCCTTGACC[C/G]TACAGTGTTAAATGA | 11059 |
rs550280593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434926 | ACTGTGAGTCAAACC[A/G]TATTGTAAAACCTGT | 11059 |
rs550298408 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86371282 | TCTACCAATGGACAT[C/T]TGAGTATTTTTCAAT | 11059 |
rs550307033 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAA | 0.210301 | 0.246828 | intron-variant | WWP1 | GRCh38.p7 | 8:86451215 | AGACCCTATGTTATT[-/AAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 11059 |
rs550317484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86427487 | ATTAGTGGTAGAATG[A/G]GAAGGTAATTTAGGT | 11059 |
rs550340899 | snp | C/T | 6.61605e-05 | 0.00575116 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442681 | GCTTATTTGAGTATG[C/T]GGGCAAGAACAACTA | 11059 |
rs550381396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464157 | CTTGATTTCAAACCC[A/G]TATTGTGCATTCCCT | 11059 |
rs550400136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392958 | ATACACAAACGTAGC[A/G]TATGACAGCACCCAT | 11059 |
rs550429278 | snp | C/T | 0.000798881 | 0.01997 | intron-variant | WWP1 | GRCh38.p7 | 8:86414300 | GCAATCTGGTATACA[C/T]AGAGATATTTATATA | 11059 |
rs550436769 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86387499 | TATATTTATTTATTT[A/G]TTTATTTATTTTATC | 11059 |
rs550466199 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | WWP1 | GRCh38.p7 | 8:86388433 | GATCAATTCTGGAAG[C/T]TCCTTGAGTATTTTC | 11059 |
rs550468184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86456885 | ATATCACAAAAATAT[A/G]TATGTATGCATATAT | 11059 |
rs550502853 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410327 | ATGATATTAGAACTT[C/T]CATCACCTTTTCCAT | 11059 |
rs550530499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86422643 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 11059 |
rs550544901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458541 | AGTGTACCACACTAA[C/T]CTTGAACATTTTATT | 11059 |
rs550555367 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358743 | CGAACTCCTGGGCTC[A/T]ATTAATCCACCCACC | 11059 |
rs550590842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86357924 | TCACGGCTTGGTGTT[A/G]GTATCCTACCACCAT | 11059 |
rs550594812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449819 | TATACACATTACTCC[A/G]TAGCTTACTTTTTTT | 11059 |
rs550613465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350176 | TCTCCTTTCCAAGAA[C/T]AGGTAGATTCATTGA | 11059 |
rs550670011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415291 | CTTTATTTTCCCCAA[C/T]ATTTTATGTTGAAAA | 11059 |
rs550671935 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445781 | TTCTGAACAAAGTAT[A/G]TGTCTCTTTTTTTTC | 11059 |
rs550682195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393411 | TGCCACCATGCCTGG[C/G]TAATTTTTGTGTTCT | 11059 |
rs550683828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366519 | TTCTCCTGACATGTA[A/G]TTCCAGTGATATGAT | 11059 |
rs550708769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435355 | AGAAATCTTCCTGTG[A/G]TATTTTGTTGGACTT | 11059 |
rs550714430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351667 | TAAAAGGGTAAGCAC[A/G]AAATCTGGGATACTG | 11059 |
rs550771990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86388085 | TAGCCATACATGGCC[G/T]CTGGCTACTGTATTG | 11059 |
rs550776063 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86387210 | ATATATATTAAATGA[-/C]CCTTATTTTCACATT | 11059 |
rs550777859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86352198 | TACAGGTGTGTGCCG[C/T]GACACCTAGCTAATT | 11059 |
rs550868496 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355647 | AATTATGTGTTAAAC[A/G]TGATCTCTAACAGCT | 11059 |
rs550889422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444572 | TCAAATAGGAGTGGT[C/T]CCCAGAGGACAAGGG | 11059 |
rs550917752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414931 | GATTAGGCAACTGGG[A/T]CATGGCATATTTGAC | 11059 |
rs550925116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413553 | AAAGCTATGACACGT[A/C]AGTGGATTCTGAAAG | 11059 |
rs550943688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373236 | TTTGAAATTTAGTGA[G/T]ATTTTCATTATATTT | 11059 |
rs550946891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86389329 | GTGTTTGTGTCCCTG[A/G]GTACTTGAGATTAGG | 11059 |
rs550980534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373930 | TAATTTTCATGTACT[A/T]TTTGAGAACTTCTTA | 11059 |
rs550987331 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443345 | TCCCAAAGTGCTCAG[A/G]TTACAAATGTGAGCC | 11059 |
rs551046636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408986 | GTCTGTTCATTTTGC[C/T]GAAATGTTTTAGCTC | 11059 |
rs551062945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359581 | ACTTTCTTTCCAGAC[A/G]TTTTCAAAGATAAGC | 11059 |
rs551067622 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86456803 | TCCAACAACAGCATG[A/G]ATGAATCTCAAAAAC | 11059 |
rs551125537 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86401779 | GAATGAATACACTTA[G/T]AACTGAAAAGTAATT | 11059 |
rs551128879 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386457 | CTCTCCCTTCCTTTC[C/T]TCCTCGTTCTTCTTT | 11059 |
rs551149643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86442527 | TTAAAGACTGTTGAG[C/T]AGAGGTATGATGTAT | 11059 |
rs551175358 | in-del | -/ATAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391058 | TGTGTTATTACAGCC[-/ATAA]ATAAACCTTATTTAC | 11059 |
rs551187907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86399350 | TCAGAAACTCCCTGG[C/T]ATTCACAGTTCATGA | 11059 |
rs551192584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86445171 | TAGTCTATTAGTTGC[A/G]GGTCAAAATTCTTTG | 11059 |
rs551277104 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361167 | TTGGGAGTGAAGAGT[C/G]GGGCAGGAAGACCAT | 11059 |
rs551282223 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342545 | ATGCTCGGGGGAGGC[A/G]GATTCCGGGTCCGGA | 11059 |
rs551290807 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86389761 | CCCCCACCCACCTCC[A/C]GGATGGGGCGGCTGC | 11059 |
rs551291784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394808 | TATAACTCAATCTTC[C/T]ATGTTCAGAATTGTG | 11059 |
rs551373278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465150 | AACACGGCTAAGATT[G/T]CTAGGCAAAATTGGA | 11059 |
rs551385597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391276 | TTTGCTCCTTTAATC[C/G]TCTAATACATTGTCT | 11059 |
rs551387749 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86364588 | GGGTGGGAGGCTCAC[A/T]TGAGCTAAGGAGTTC | 11059 |
rs551388033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355984 | AGTTTCATGGCCCTG[C/G]GCAATTTACTTCAAC | 11059 |
rs551412033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465565 | TTCAGCCTGGGAGGT[A/C]GAGGTCGCAGTGAGC | 11059 |
rs551420790 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412782 | CTTAATTACGGTTTC[A/T]GCCTTTGGTCTTCCT | 11059 |
rs551424861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86356630 | GCCAAAGAAAGCCCT[A/G]TGTTTTTGTCTGTCT | 11059 |
rs551430074 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353725 | TGACCTCAAGTGATC[C/T]GCCTGCCTTGGCCTT | 11059 |
rs551433298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379198 | GTCTGGGCCTTCTAT[A/G]TTAGTCCAGTGGCGC | 11059 |
rs551458275 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86449667 | AAAATCAAACTTTTC[A/T]TTTTTCCTAGATATT | 11059 |
rs551465020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372617 | TTATATATGATGTGC[A/G]GTAGGGGTCCAGTTT | 11059 |
rs551466829 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383285 | TATTATTATTTAACC[A/G]TATTCCCATTGTTGG | 11059 |
rs551498451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458243 | GAGTTGAGTGACAGA[A/C]TCTTATTTAAGTAAT | 11059 |
rs551552091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86358595 | TCAAGTGATTGTCCT[A/G]CCTCAGCCTCTTGAC | 11059 |
rs551560323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343607 | TTACGACCTTTAAAT[A/G]ATCAGTCTTGTTCAC | 11059 |
rs551576359 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86392931 | CCTTTCTGAAAAGTT[C/G]TACTAATTTATATAC | 11059 |
rs551588900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359532 | GTCTCCTACTTCACC[G/T]AGAAAATTGGAGACA | 11059 |
rs551660911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387414 | GACCATAATCTTGAT[G/T]TCTAATCTTTTAAAA | 11059 |
rs551689901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351622 | GGCATGAGCCACCAG[C/G]CCTGGCCAAATAAAC | 11059 |
rs551704885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86428224 | CTATTCTGATTCTCT[C/T]CCCAGATTCTAAGAA | 11059 |
rs551778004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379903 | ATGTGGAGAAATCAG[C/T]GTATATTGTTGATAG | 11059 |
rs551778297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389254 | AGGGAAGGTCAGCAG[A/G]TAAACATGTGAACAA | 11059 |
rs551785761 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | WWP1 | GRCh38.p7 | 8:86378329 | GAATATATCATATCA[-/T]TTTTTTTAAGCCTTT | 11059 |
rs551787248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393749 | TCATACTTTTGAGTA[A/T]GTTGGCCAGCCTCTA | 11059 |
rs551788871 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418197 | TATTTATTAAACTCC[A/T]TGTCTGTGTGGCAGG | 11059 |
rs551792733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86460954 | AGCTGGGACTACAGG[C/T]GCCCGACACCACGCC | 11059 |
rs551813177 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86381184 | TTTGTGTATAGTAAA[A/C]GTATCATGTAAGTCT | 11059 |
rs551816954 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86389703 | TGGCGGCCAGGCAGA[C/T]GGGCTCCTCACTTCC | 11059 |
rs551819550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373199 | AACTTAATTGTATTA[C/T]GGACAGAAACTTAGA | 11059 |
rs551858778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366332 | GGGTATGATGGCATG[A/G]GGATGATGGGTGATG | 11059 |
rs551898570 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86381906 | TTATTATATTCTTTA[A/C]AACTTGAGAAAATTA | 11059 |
rs551976718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408024 | TATCATACAGAATAG[G/T]TTTACTACTCTAAAA | 11059 |
rs551989033 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366958 | AATGAAATATTTATT[C/T]TATGCTTTGGAGTTG | 11059 |
rs551999990 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392834 | CAATGATGTAAGTGC[C/T]TCTTTATTCTTTCGA | 11059 |
rs552001697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422918 | GATGAAAGAATTTTC[A/C]TGGGGCAGTATCACC | 11059 |
rs552015211 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86408922 | CTCAAAAAAAAAAAA[A/T]TTTTTTTTCTTCGGA | 11059 |
rs552016485 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86451273 | CATGAAAGCTTGCCC[G/T]ATAGAGGGAGATTTT | 11059 |
rs552032335 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86374340 | AAGATATAGCCTCTG[C/T]AATGGTGGGAGAATT | 11059 |
rs552037273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409703 | CATCTCTACCAAAAA[A/C]TAGGAAAACTAACCA | 11059 |
rs552122910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86402306 | TAGTCTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT | 11059 |
rs552145475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344926 | GACCTTGGATTTACC[C/T]GGTGGTGGGGCTTCC | 11059 |
rs552195794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368705 | CACTGTCCTTATGTT[C/T]CATTGTCCACTATGC | 11059 |
rs552232134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437063 | ATTCATGGTAGACTT[C/T]ATTTTGCTTTTTACC | 11059 |
rs552232184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429405 | TAAATATTGAGTATA[A/C]TTAACTGGGTCTGTT | 11059 |
rs552255745 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86438035 | TCAATCTCCTGACCT[C/T]GTGATCCACCTGCCT | 11059 |
rs552303521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86423800 | CCCAGAAGGGGCGGC[C/T]GGGCAGAGGCGCCCC | 11059 |
rs552319566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430181 | ACCCCAGTCTGGGTA[A/G]TAGAGCAGGAAGATC | 11059 |
rs552332125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86374913 | AGACAGGGTCTCACT[A/G]TGTTGCCCACGCTGG | 11059 |
rs552343317 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86439112 | ACTTTGGGAGGCCAA[G/T]GCGGGTGGATCATGA | 11059 |
rs552343578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86431290 | ATATAAGGGATACAT[A/G]TATCCCTGATATGTT | 11059 |
rs552384101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432279 | TGTCTTTGCATAACT[A/G]AGAAAATAGAAGCAA | 11059 |
rs552391999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86446341 | CCAGTTTTTAATGGG[G/T]TTTTTTTTCTTGTTG | 11059 |
rs552417430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368211 | TAATTCACATTGTAA[C/T]ATGAGATAGATGACT | 11059 |
rs552449457 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467235 | AGCCATTCATTCATA[A/C]AGATCTGGATTTGCT | 11059 |
rs552475673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460128 | TTACCCATTTATGTC[A/G]TTGAAAATAACCAGT | 11059 |
rs552512397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86460903 | CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT | 11059 |
rs552519461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390423 | GAGCACTGAGTGAGC[G/T]AGACTCCGTCTGCAA | 11059 |
rs552520356 | snp | G/T | 0 | 0 | intron-variant | WWP1 | GRCh38.p7 | 8:86453136 | TATTCACATTGTGCA[G/T]CCAATCTCCAGAAAT | 11059 |
rs552560999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352370 | GCTGGGATTACAGGT[A/G]CATGCCACCAGGCCC | 11059 |
rs552621165 | in-del | -/GTGCTTTGTCACTAAAATGACAAAAGTAGTGTAC | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86363882 | CAGGAAGTATTTTTA[lengthTooLong]GTGAAACACATTTTC | 11059 |
rs552638481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395844 | CCAACTAGTCTGTCT[G/T]TTGAGGATGAGAATG | 11059 |
rs552665787 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376526 | GTGAGCCGAGATGGC[A/G]TCACTGCATTCCAGC | 11059 |
rs552671158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346567 | GTGGATTAAGTAGCT[A/G]GCTAGTACGGTTAAA | 11059 |
rs552676928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390132 | TCCCCACATCTCAGA[C/T]GATGGGCAGCCGGGC | 11059 |
rs552677801 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86435083 | TTTGGGTTTTAGGTT[A/C]GGCTTAGGATGTGGT | 11059 |
rs552684201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427091 | TCACTTGAACCTGGG[A/C]GGCAGAGGTTGCAGT | 11059 |
rs552687115 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421902 | TTTGATCCTCTCTCA[A/G]AATTTTGCAGATGGG | 11059 |
rs552700236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414731 | TGTTAACCCTTTACT[C/G]TCCACATTTTTTAAT | 11059 |
rs552797810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415379 | GATTTTACAATTGAC[C/T]CTTTATTGTGCTTGC | 11059 |
rs552799750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450221 | TGGCATTCTTGGCCT[C/G]TTCTTATTTTTCTGC | 11059 |
rs552823644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382971 | CTTTAAAAAGGTTCT[C/T]TCTGCAAATCCACAT | 11059 |
rs552829955 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440446 | TAGATATAAATTTCT[C/T]GCACACTTGTTTTTC | 11059 |
rs552851251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424636 | AGTGAAACCCCGTCT[C/T]CACCAAAAAAATACG | 11059 |
rs552893288 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464679 | CGCCACTATGCCTGG[C/G]TAATTTTTTAATTTT | 11059 |
rs552922612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435082 | GTTTGGGTTTTAGGT[C/T]AGGCTTAGGATGTGG | 11059 |
rs552930857 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86444185 | ATTCTGGGTATATTG[C/T]GAAGTTAGAACTAAC | 11059 |
rs553086217 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344986 | ATTTGAACACTTTGT[A/T]TCAGAAGGATTAGTG | 11059 |
rs553087525 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368161 | TCGTGTCATATACTC[-/T]TAAGTGCTAAGTGTT | 11059 |
rs553097409 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370053 | AAAACCTCTCTGATT[A/C]CATATTCTTACCTTT | 11059 |
rs553146702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372767 | TTCCTATTTTGTTTC[A/G]TTTTTTTCCCCTTCG | 11059 |
rs553172681 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463432 | CTGCCTCAGCCTCTC[A/G]GGTAGCTGGGATTAT | 11059 |
rs553208357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408421 | TACTTTTGTAACAAA[C/T]GGCCAAACTGTCTTC | 11059 |
rs553219752 | snp | A/G | 5.00914e-05 | 0.00500432 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380764 | AAAAAGAACTGGTTC[A/G]GAACAGCAATATATA | 11059 |
rs553237770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466602 | TTTGTAATTCCATTT[G/T]CCTCTTGGAGATGTT | 11059 |
rs553292174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351198 | GAACGTAAGCCCTTA[A/C]ATCATGTTTATTGCT | 11059 |
rs553295014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367807 | CATACCACTATGCAG[A/G]TTGTTGTCCCTGAGG | 11059 |
rs553296199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86401214 | GTATATGCTAATTTG[C/T]AACTAATATTTGAAG | 11059 |
rs553300847 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466984 | AAGCTGTTCATTCTG[A/T]ACAGTGAATTTTCCG | 11059 |
rs553322185 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383808 | AGGATACGGATATGC[C/T]CAGGAAAAATAAAAT | 11059 |
rs553329778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368511 | TAGTTCAGATAAGCT[C/T]ACTATCTTAAATCTA | 11059 |
rs553331839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360197 | ACATCTTTTACGCTT[A/C]TGTTTCTCTTTGATA | 11059 |
rs553416524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459527 | CAGAGAAAAAACTGG[A/C]AACAGTTCTATAGAG | 11059 |
rs553422039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437953 | TACAGGCGCCCACCA[C/T]CACGCCTGGCTAACT | 11059 |
rs553432892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86375146 | TAATTTAAAAAATTA[C/T]CAAAAACAATAGGTC | 11059 |
rs553493776 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86388749 | TATTTAAACATCTTG[A/G]TAGATTATATTAGCC | 11059 |
rs553497908 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86435978 | TGCTGGGATTACAGG[C/G]TTGAGCCACTGCATC | 11059 |
rs553523663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395276 | TGAGCATAAAGGCCG[C/T]ATATGGTTTCTGTTA | 11059 |
rs553547881 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86381424 | ACATTACTGAAATAA[A/T]TGCTTTAATAGGAAT | 11059 |
rs553560842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389934 | ACGCTCCTCACTTCC[C/T]GGACGGGGCGGCTGC | 11059 |
rs553564311 | in-del | -/CGGAGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353515 | TTTCTTCTTCTGAGA[-/CGGAGT]CTCACTCTGTTGCCC | 11059 |
rs553624934 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379633 | CATATCTCAGGTATA[C/T]TAGATTTTCACTTTC | 11059 |
rs553631460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86423370 | GGCAGAGGACCCTGC[A/G]GCCTTCCACAGTGTT | 11059 |
rs553647213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390234 | CCGGGCAGAGGGGCT[C/T]CTCACATCCCAGACG | 11059 |
rs553679231 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366291 | GGGTGAGTTGTTGGC[A/T]TAGATGCAGAGGCTG | 11059 |
rs553693200 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413378 | GTCAAGAACCTCATC[A/G]TCTAAGTGGTGGGGG | 11059 |
rs553696202 | in-del | -/TG | 0.426141 | 0.17741 | intron-variant | WWP1 | GRCh38.p7 | 8:86414230 | AAGTTTGTTTTTCTG[-/TG]TGTGTGTGTGTGTGT | 11059 |
rs553716061 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365653 | TATAGGGAGAGGTCA[A/G]GTGTGGACAAGAAAG | 11059 |
rs553717404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416275 | CTTTCTGTGTGAAGA[C/T]AAAGGGAAGGAGGAA | 11059 |
rs553743739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460453 | CTTATATGTACAGTG[A/G]GGATGCTAATGATTC | 11059 |
rs553765453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86383729 | CCTGGGCTACAGAGC[G/T]AGACTCCCTCTCAAA | 11059 |
rs553777479 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86392277 | AGAGAGAATCTTTGT[A/C]ACTATACCCATAGGT | 11059 |
rs553778467 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86410030 | AATCATATGACGTTT[A/T]TCCTTTAATCTGCTA | 11059 |
rs553779660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417782 | ATAGAAATATTAATA[G/T]TTCTTAAGCTCACCA | 11059 |
rs553800164 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345975 | CAATGATGGTGTTCT[C/T]TCATGTATGAAGATA | 11059 |
rs553817368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402503 | CTTTTTTGGCAACTG[A/G]CTGGTCTCGAACTCC | 11059 |
rs553819816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449629 | TGAACTACAGATGAC[A/G]CATCTTAAAATGTAA | 11059 |
rs553837333 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449717 | TATGAATAGTACTAC[C/T]ATTTTCACCCTCTTA | 11059 |
rs553861397 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342222 | GGCTAAATGCAATTA[C/T]TTACTCTTGCAATGT | 11059 |
rs553863587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86418244 | GTTAGTATACTGATT[C/T]GCAAAACAGTTGAAG | 11059 |
rs553878344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352598 | TTGAACTCCTGGACT[C/T]AAGTGATCCTCTCAC | 11059 |
rs553882878 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447137 | TCATAGAGCAGTCAG[C/T]TTGGTTGTTTATGCA | 11059 |
rs553890374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345951 | AAAGTGGAATCAGGA[A/G]ATTGTTGACAATGAT | 11059 |
rs553900289 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404235 | TCTGAAACATTTCTG[G/T]TTCCAGGCATTTTAG | 11059 |
rs553901767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411973 | TTTCATTGTTCAGAA[C/T]TTTGAAATCTAAGTT | 11059 |
rs553901780 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86419004 | CCACAATCCACAAGC[C/T]CCACCCAGGCACATA | 11059 |
rs553903774 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430634 | CCACATGCTTGGCTT[A/C]TTTCTACTTTCATAT | 11059 |
rs553904962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424742 | GAGGTTGCAGTGAGC[C/T]GAGATGGCAGCGGTA | 11059 |
rs553965588 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393401 | TGCAGGCACGTGCCA[-/C]CATGCCTGGCTAATT | 11059 |
rs553971256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394895 | ACAAATCTTTGTGGC[A/G]TTGATGATTTTGCAA | 11059 |
rs553984388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412583 | GACACGTGCTTTCCA[A/G]CACAGTTTACAGTGA | 11059 |
rs553985361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437887 | TCACTGCAAGCTCCA[C/T]CTCCCGGGTTCACAC | 11059 |
rs553985431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446179 | TAGAGATGGGGTTTC[A/C]CCATGTTGGCCGGGC | 11059 |
rs554041348 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431725 | CATTCAAAGATCCTC[A/G]CAATGGGAAGTCATC | 11059 |
rs554069885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86383267 | ACAGTACCTTGCCTG[A/G]ATTATTATTATTTAA | 11059 |
rs554070856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438734 | TGTATACAGGGAAAG[C/T]ATTCTTCAAAACATA | 11059 |
rs554105290 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86424308 | CGGGAAGAGGCGCTC[C/T]TCACTTCCCAGACTG | 11059 |
rs554129379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424398 | CCTCACTTCCCAGAC[A/G]GGGTGGCGGCCGGGC | 11059 |
rs554243075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366838 | TACTCTTTCATTTTA[C/T]AAATTCATTGAAATG | 11059 |
rs554295434 | snp | C/T | 0.00263108 | 0.0361748 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468374 | ATCTGCTTGGTTGAA[C/T]AGACTCCTTTTCCAA | 11059 |
rs554310586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401936 | AAAGAAACTTAAGAG[A/C]ATTTAGTAAATCCTA | 11059 |
rs554332455 | snp | C/G | 0.000165325 | 0.00909038 | intron-variant | WWP1 | GRCh38.p7 | 8:86461862 | GTAAGTTCAAGAATC[C/G]TAAATACGAAGGTGA | 11059 |
rs554347635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86402388 | CCTCTTGGGTTCAAG[C/T]GATTCCCCTGCCTCA | 11059 |
rs554387381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86362708 | GATGACAGTGTGTAG[A/G]TATACCACTTCAGAA | 11059 |
rs554392853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404561 | AAAATAAAATGGATG[G/T]GAGGAACATGAAGGT | 11059 |
rs554397152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447046 | ATGAAATAGTCATCT[A/G]GGAAAGTGGGAGAGT | 11059 |
rs554415298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354671 | TTATAACAAAATGTG[A/G]CAGTACTGTATTCCT | 11059 |
rs554432000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397060 | CGGTGATTAGTAGTT[C/G]TAGATTTTTGTCTTG | 11059 |
rs554451358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86444968 | GACTGTGCAGGCTGT[A/G]CAAGAAGCATGGTGC | 11059 |
rs554495074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347243 | CTCCCACCATGGCCT[C/T]CCAAAGTGCTGGAAT | 11059 |
rs554565446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86423177 | AATCCTAGATAAATA[C/T]CAAATGTCAGAAAAA | 11059 |
rs554571315 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393740 | CTGTTTTTCTCATAC[G/T]TTTGAGTATGTTGGC | 11059 |
rs554578554 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WWP1 | GRCh38.p7 | 8:86424048 | TCCTCACTTCCCAGA[C/T]GGGGCGGCTGCCGGG | 11059 |
rs554635135 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86424628 | GCCAACACAGTGAAA[C/G]CCCGTCTCCACCAAA | 11059 |
rs554644586 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452268 | GATTTGGCTATCTTA[C/T]TAAATAGTGAAGAAC | 11059 |
rs554650374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360007 | TGAGCTGAGATTGCG[C/T]CACTGCACTCCAGCC | 11059 |
rs554661358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438231 | TCCTCATTCTCATTG[G/T]CTTCACATTGAATAG | 11059 |
rs554683835 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86390180 | CCTAGACGGGATGGC[A/G]GCCAGGAAGAGGCGC | 11059 |
rs554687889 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456339 | CCTACACCCTGGGAG[-/A]AACTATTGAGACAAA | 11059 |
rs554707359 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374924 | CACTATGTTGCCCAC[G/T]CTGGTCTTGAACTCT | 11059 |
rs554709337 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402786 | CCACAAAAAATACTA[C/T]GTAATTCATGATATA | 11059 |
rs554716729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86383056 | AAGAAAATATAATTA[C/T]GGATTATAATAATTA | 11059 |
rs554724498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86433905 | CCTAGGCAACAAGAG[C/T]GAAACTCCATCTTAG | 11059 |
rs554728406 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346302 | GTGAAATAAGAAACT[G/T]TAAGAACTTTATTGG | 11059 |
rs554749912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451758 | CTGTGGCTTCTCTGT[A/G]TGAGGTGGTGTATGC | 11059 |
rs554786573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452365 | AATAGTTAACAATGT[G/T]TTAGAACTGATTTCC | 11059 |
rs554799186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453534 | TTTCTTTGAGATCCC[A/G]TTTCTTTTGGATATG | 11059 |
rs554805609 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86451611 | ACGGGACAAAGAGGG[-/T]TTTAGTAATTGAAGA | 11059 |
rs554868921 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86446947 | TTTCTTCTGGTTGCT[-/TC]TGTTTCCTCTGTGAA | 11059 |
rs554871854 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468262 | ACATACAGAAAAACA[C/G]TAATTATTGTTTTGC | 11059 |
rs554874481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445414 | TGTGTGCCCAATGCT[A/G]AGCTCCCACCTGTAC | 11059 |
rs554880375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352525 | TGAGCCACCGTGCCC[A/T]GCCTAATTTTTTATT | 11059 |
rs554880478 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345196 | CTGATCCAGGTTGGT[G/T]GGGAGAACAGTGGTA | 11059 |
rs554908278 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395740 | TTTGCAAAAATTTAT[A/G]AATTAGAATTGCAGA | 11059 |
rs554962284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382415 | TTAAAAACCAGGGTT[C/T]TAGCTGGGGGTGGTG | 11059 |
rs554966873 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347233 | ACTCGTGGCCCTCCC[A/G]CCATGGCCTTCCAAA | 11059 |
rs555110726 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418957 | ATTGTTCTCTAACAA[A/G]ACAGTCCCATTATTA | 11059 |
rs555162633 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | WWP1 | GRCh38.p7 | 8:86461349 | CACTGTAATTTCTCT[A/G]TACGTAATTTTGTGA | 11059 |
rs555171960 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415895 | TATTTCTATATTCTT[C/T]GTGCTCAAAACTATG | 11059 |
rs555174196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440260 | ATAGTTTTAATGAAT[A/G]TAGCTAGTTCCTCCA | 11059 |
rs555177185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86369170 | AATACTCCTGAGGCT[C/T]AGTTTTCTCATCTCT | 11059 |
rs555193143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411117 | GCCATCATACAGTTC[C/G]TACTATTGGCAAAAC | 11059 |
rs555280379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86370846 | GTATTGCTTATAGCT[A/G]TATTCATTCTTTTTT | 11059 |
rs555290525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384856 | AGATACAAAAAATTA[G/T]CCAGGCTTTATCAAA | 11059 |
rs555291579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353515 | TTTCTTCTTCTGAGA[C/T]GGAGTCTCACTCTGT | 11059 |
rs555317568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371381 | TACTCATTGAAGGGC[A/G]TACAAATGTTTAGCT | 11059 |
rs555319369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363604 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 11059 |
rs555323290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377225 | CAAATAGCTGAGATT[A/G]CAGGTGCATGCCAGC | 11059 |
rs555328087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390855 | GTTATTGAGGTCATT[C/T]GTTCCTTTTCAGATT | 11059 |
rs555368190 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444368 | GAGATGTAAAAGAGA[C/T]AGTTGGAGGTATAAG | 11059 |
rs555375198 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362019 | ACACATATATATATA[C/T]ACATATATATACACA | 11059 |
rs555400910 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396413 | TGCTTTTGTAGTTTT[-/TG]TGTGTGTGTGCTTTC | 11059 |
rs555406105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439424 | ATCTTGAACTCCTGA[A/G]CTCAAGAGATTCCCC | 11059 |
rs555442897 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86432563 | AGCAAAAAAAAAAAG[A/G]AATTACAACTCTTCC | 11059 |
rs555471567 | in-del | -/TCT | 0.470132 | 0.118498 | intron-variant | WWP1 | GRCh38.p7 | 8:86430798 | GATATATATCTCTCC[-/TCT]ATATATATATATATA | 11059 |
rs555490352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390563 | GTCAGGCGTGGCAGC[A/G]GGCGCCTGCAATCCC | 11059 |
rs555490417 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86397732 | TTAAATAAGAACTAG[A/G]TGTTCTAATAATGGG | 11059 |
rs555527440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413413 | GAAGAGAAGTAGACA[A/G]TCAGCCAGCATACAG | 11059 |
rs555531653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456417 | AAAAAGATAAGAAAA[C/T]ATTTTTAAATGGACA | 11059 |
rs555532393 | in-del | -/GA | 0.0107246 | 0.0724382 | intron-variant | WWP1 | GRCh38.p7 | 8:86424600 | CGCCGTTAGGAGCTG[-/GA]GAGACCAGCCCGGCC | 11059 |
rs555543563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391955 | TGTAAGCCGTTTTTA[A/G]TAAATGCTCTAAGAA | 11059 |
rs555555971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86406034 | AGGGGATCCATCTGA[C/T]GGTTTAGTTGCTATG | 11059 |
rs555585296 | in-del | -/TTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370881 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGAGTCTTTC | 11059 |
rs555629001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392536 | CATTAAGTTCAATTC[A/G]AAGTAAATTATGTCC | 11059 |
rs555636689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425516 | GACTGTCAAGCATTG[A/G]CATGAGTTACTGAGA | 11059 |
rs555671178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86377609 | TTGATCATGGAACGC[A/G]GAAAAACTGATGGAA | 11059 |
rs555696000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412695 | ACTATGTTAGTGTAC[A/G]TTGGTTTTTTTTTTG | 11059 |
rs555704118 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364911 | GTAAAATTAAAAATT[-/A]AAAAATACAATTGAG | 11059 |
rs555723788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361838 | CACCCCTTTCTGTCA[A/G]TGAACTTAAAATTGA | 11059 |
rs555786714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86434446 | TCTTTTCCCGAAACT[C/T]CATATGGCTTTTGCC | 11059 |
rs555812903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86386774 | CTTACTGCATTTGTT[C/T]TGCTGTAACAAAATA | 11059 |
rs555893516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347225 | ACTCCTGGACTCGTG[A/G]CCCTCCCACCATGGC | 11059 |
rs555903555 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392017 | GTTACAACAGACAAT[A/G]AATTCTTTTGGCAGC | 11059 |
rs555932022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428355 | TACTTATTGCCATAA[A/G]CAAACATCCGTGAGA | 11059 |
rs555940748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448622 | TTGGGAAGTTCTTCT[C/T]ACCAGTACCAATGTT | 11059 |
rs555966829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86390421 | TTGAGCACTGAGTGA[A/G]CGAGACTCCGTCTGC | 11059 |
rs555975632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449196 | AAATGTAGGCATTTT[A/T]CCAAGATTTTATTTC | 11059 |
rs555995450 | snp | A/G | 0.000511117 | 0.015978 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398593 | TACAGGAAAATGGTG[A/G]TGCCTTACATGAAAA | 11059 |
rs555996760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446918 | AGTGAGCAGATATAG[A/T]AGAACACAAAAGTTT | 11059 |
rs556053895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86396888 | AGAGGCGTGAGCCAC[C/T]GTGTCTGGCCTTAAT | 11059 |
rs556063353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442167 | AATACAAAAAAATAC[A/G]TGGCTTTTGCCTTTG | 11059 |
rs556074581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376452 | CACATGCCTGTAATC[C/T]CAGCTACTTGGGAGG | 11059 |
rs556082670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439334 | GGTGATGGAGCAAGA[C/T]GCTGTGTCAAAAAAA | 11059 |
rs556094435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390510 | CCAGCCCGTCCAACA[C/G]GGCGAAACCCCGTCT | 11059 |
rs556132996 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343156 | GCCCGGAGTTCGCCC[C/T]GGCAAAGGCCTGTGC | 11059 |
rs556136754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444937 | TGGATAATTTATAAA[A/G]AAAAGGGGTTTGTTT | 11059 |
rs556172422 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419148 | ACTAGGGCTGGGCGC[A/G]GTGGCTCCCGTCTGT | 11059 |
rs556180137 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354970 | CCTCACAATACTATA[C/T]TAATTTGGTGTTATT | 11059 |
rs556206111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86396303 | ACGGGGTTTCACCAC[A/G]TTGGCCAGGATGGTC | 11059 |
rs556235396 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86438802 | CAGAATTTTTCTCAA[A/C]AATACACACGGTAAC | 11059 |
rs556238732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403410 | AAGAGATTCTTGTGC[C/T]TCAGCCTCCTGAGTA | 11059 |
rs556269694 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467996 | ATAATTATTTTTGTC[A/C]TAACACTTTTTAATT | 11059 |
rs556294395 | snp | C/T | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86390269 | GCGGCCAGGCAGAGA[C/T]GCTCCTCACTTCCCA | 11059 |
rs556305890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405102 | TGATTGTTCATCACT[G/T]AATAAAGGATGAATT | 11059 |
rs556325894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419102 | TAGAGATCAAAAAAA[C/T]AACCTAGAAAATACT | 11059 |
rs556333242 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | WWP1 | GRCh38.p7 | 8:86394328 | AGGTCTAGGAGGTAC[-/A]AAAAAAATCAGCTTC | 11059 |
rs556344528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86397976 | ATACACAGCCAATAA[A/G]TAGCAGAACTGGAAT | 11059 |
rs556411344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445806 | TTTTTCTGAAGCCTT[A/G]CCAACATCTGTTATT | 11059 |
rs556426121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432500 | CAGGTTTTATTTCTC[C/T]ACAAAATTATTCTTA | 11059 |
rs556431793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398817 | TTACAGCTTTATTGA[G/T]ATATCATACATATAT | 11059 |
rs556443018 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424697 | GCAATCGCAGGCACT[C/T]GGCAGGCTGAGGCGG | 11059 |
rs556516249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424907 | TTCTTGATTCAATTT[C/T]TGTTTTCTGATAACT | 11059 |
rs556518327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432936 | TATTGCTCCCCTTTA[C/T]AGGAAAGCTACTTGC | 11059 |
rs556543673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86369972 | CAAGTCAATAATAAA[A/G]AACATTTGGGAACCA | 11059 |
rs556549554 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86448617 | TGCCTTTGGGAAGTT[A/C/G]TTCTCACCAGTACCA | 11059 |
rs556550305 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381257 | CAGTAAGACTCCTGT[A/G]TTGGTGTTTTGGCTT | 11059 |
rs556570908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86434415 | TCTTAGCCTTTATTC[C/T]GTCTGCCTGGTATGC | 11059 |
rs556586150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86441202 | TATTCCTAGTTTTAT[A/G]TATGTGTCTAAACAC | 11059 |
rs556652724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462800 | TGGTTTGTGAACCTG[C/T]TTGTGCCTTAGCACA | 11059 |
rs556657863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427051 | GCCTGTAATCCCAGC[C/T]ACCCAGGAGGCTGAG | 11059 |
rs556685811 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86370132 | TTTTTAAAATACCAC[-/A]AATATGATTGTTTGA | 11059 |
rs556686881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413256 | AGCTTTCCTTTCCCT[C/T]TCAAAAATCTCTTGT | 11059 |
rs556698296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385922 | AGCCATGCACATGCT[A/C]ACATGTCCTTACTCT | 11059 |
rs556698594 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465216 | AGCAAAGAGCATAAG[C/T]TTCCTTTCCCCACCA | 11059 |
rs556699192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447818 | CCTTTTCAGGTGCAC[A/G]GGGCCCTTTTATATT | 11059 |
rs556703228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363916 | ACAAAAGTAGTGTAC[A/G]TGAAACACATTTTCC | 11059 |
rs556779250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456323 | TTAAGTGAAAAAGCA[A/G]CCTACACCCTGGGAG | 11059 |
rs556781272 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86355450 | CCAAAATATTAAAAA[A/T]TTTTGAATTTTAAGG | 11059 |
rs556794619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457309 | GAGGTTAGTATATTT[C/T]TTTATTTTCAAATAT | 11059 |
rs556896501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86464566 | TGTTACCTATGTTAG[A/G]GTGCAGTGGCACAGA | 11059 |
rs556921373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86450185 | TCTCTGCTTACCAAC[C/T]TTAATGTACCCTTCT | 11059 |
rs556924089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392370 | GTTTCAATTTTGAGG[C/T]GGAGAGAACCACTTT | 11059 |
rs556932432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342989 | GCGGGAGGGGGCACG[A/G]GCCCTGAGCCTTGGC | 11059 |
rs556936786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348715 | TCAGGTTGTAATTTT[A/G]CGGAGTGTAATTAAT | 11059 |
rs556937356 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86365160 | ATGTATTAACTCCCT[C/G]TGGTTGAAAATCTGA | 11059 |
rs557011485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86350448 | TTTGAAGCATTTCAT[A/G]TACACTAAAAAACGG | 11059 |
rs557048600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377847 | TTTTTTTAGCTATTG[C/T]GTCTTCTAAAGCATT | 11059 |
rs557080262 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438757 | AAAACATATGTGAAT[A/T]TATTGTATTAAATTT | 11059 |
rs557128281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86378583 | AAAAAAAATCTATAT[A/G]TTCTACTAACTAGAA | 11059 |
rs557147103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86443175 | CCTTGCAGACTCAAA[C/T]GATCCTCCCACCTCA | 11059 |
rs557167964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393220 | TTGTATTTATTTATT[G/T]TTTTGAGACAGGGTC | 11059 |
rs557173786 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440948 | TAGGCTCTGCTAGCT[C/T]ATCTGTTGTCTCATA | 11059 |
rs557186117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435222 | TAACTCACTAACAAA[A/G]GATCCAGCCATAAAT | 11059 |
rs557202778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387804 | GCCGGGATTATAGGC[A/G]TGACCCACTGCAACC | 11059 |
rs557216196 | in-del | -/CTTGTC | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86357990 | ATTCCAAGAAGCCAT[-/CTTGTC]CTTAAACTTTTGGGG | 11059 |
rs557216293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86372212 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 11059 |
rs557241577 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465681 | GACAGAATTTGGCAA[A/G]GGCTATATGTGAAAG | 11059 |
rs557252954 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86372675 | GGTTTCTTTAAGTGT[C/G]CCTCTTTTCTCATGG | 11059 |
rs557270999 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86373633 | ACTTGGTTGCTCTTC[A/G]TCTTAGGTACTCCCA | 11059 |
rs557307893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440330 | TGTATTGGTGGGCTA[C/G]ATTCATCAAATGGTT | 11059 |
rs557324399 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418119 | CTTTTAAAAAAAAAC[-/TT]AGTCATATTTCCACA | 11059 |
rs557373868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86373757 | GGAATCTCACTCCTT[C/T]CCCTTGTAGCAGGCC | 11059 |
rs557395599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400375 | TAGTAAACAACAGAA[G/T]ACATAAATATGCTAA | 11059 |
rs557398252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433149 | AAAAGTAGTGCTGTG[A/G]GCCATACTTTCTTGA | 11059 |
rs557400602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466058 | ACTCAGGGCTATCTC[A/T]CTAGTCACTGCTACT | 11059 |
rs557418115 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412338 | TTTTTCATTGCTGGT[C/T]AGTAATTCTTAATCT | 11059 |
rs557435928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443966 | TAAGAGTTGAGTAGG[C/G]CAATGAGTGACCTGA | 11059 |
rs557437019 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86433867 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCATTGC | 11059 |
rs557456732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86393911 | GTCATATAGGCATTT[C/T]AGGTTTTGCCTTGTT | 11059 |
rs557479485 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407997 | CATATCGTCATGTAC[A/G]CACCATTACAGTATC | 11059 |
rs557485379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401149 | TTATAGTTCTGGGGT[A/G]TAATATTTAGCTTTT | 11059 |
rs557488454 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341526 | TTCAGTCAAGAGATA[C/T]TTGTTGAATTCTGTA | 11059 |
rs557547249 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466561 | TTTTTTTAAATTTGT[C/T]TTTATCCATATTGCT | 11059 |
rs557625951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429011 | AACATCAAGTCTGGG[A/G]TAAAAGTGTAAGTGC | 11059 |
rs557626179 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360152 | CGTCTCAAAAAAAAA[A/C]CAAAAAACCAAACCA | 11059 |
rs557661929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426226 | AGTTATAGTCATTCA[A/T]TTAGTCCATTCATTG | 11059 |
rs557673841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86364186 | GCTTCACTAGCTATT[C/G]GACTTGAATTTCTGT | 11059 |
rs557679784 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86464472 | TAATCCAGTAAATAT[C/T]AGTAGCTATAATTCA | 11059 |
rs557688610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377695 | CTACTCAAGGATAGT[A/G]GCATATAGAAGTGTA | 11059 |
rs557689514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387734 | TCACCATGTTAGCCA[G/T]ACTGGTCTCGAACTC | 11059 |
rs557727617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371414 | AAATGATAATGCCAA[A/G]TTATTTTCCAACAGG | 11059 |
rs557747548 | snp | A/G | 0.000132336 | 0.00813331 | intron-variant | WWP1 | GRCh38.p7 | 8:86398668 | TTGAATATGGGTGGC[A/G]ACATGATGTGGAACA | 11059 |
rs557799763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391161 | TAACTGCGTCTTGTT[A/G]GGGAGATTGTTCCAC | 11059 |
rs557800200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357185 | CAATATGTTCTATGT[G/T]CCAATTCTCATTTAA | 11059 |
rs557836985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86358007 | TGTCCTTAAACTTTT[A/G]GGGTCTAATGTTTGA | 11059 |
rs557837680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425646 | ATAGTGATCTAAACT[A/G]TGTTATTTCATAAGA | 11059 |
rs557838622 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363500 | AAGGCTACTGAAAGA[A/G]GTTAAATTATATGTC | 11059 |
rs557868363 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342062 | CAGATTGTTGTGTGC[A/G]TTAATTGTGCGGACA | 11059 |
rs557883868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391795 | TTTGGTAGCTGGCAA[A/G]TAACGAAGTCAGGAT | 11059 |
rs557885664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384905 | GGCATGTGCCTGTAG[C/T]CCCAACTACTTGGGA | 11059 |
rs557901223 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387909 | TCAGTAAGGGCTGCT[A/G]TCCAACAGAACTTCT | 11059 |
rs557953737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399713 | AAATGTTGTCAATTG[C/T]ATAGTAAGACGCTTT | 11059 |
rs557968001 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415601 | GAATTTTGGCAAATG[C/T]GTATGTCTGTGTAAC | 11059 |
rs557998151 | snp | A/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342019 | AGTTGACTTTTCTGT[A/T]AAATGCAGACAGTAG | 11059 |
rs558012055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349834 | AGTAGTGATTTACCC[A/G]ATCTCGTGAATTGGA | 11059 |
rs558024127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343406 | CTCTCCGTTCTTCAC[C/G]GACTCTGCAGCTCCC | 11059 |
rs558066517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388358 | CTCCTGGACTCAAGC[A/G]ATCCTCCCACCACAG | 11059 |
rs558078110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86372124 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 11059 |
rs558082105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456473 | CACAGATGGCAAGTA[A/C]ATACTTGAAAAATGC | 11059 |
rs558104627 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390035 | TGGCGGTCTGGCAGA[C/G]ACACTCCTCAGATCC | 11059 |
rs558137560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86413966 | CCGGCATTCCAGTTC[A/G]AAACAGTAAGTACAT | 11059 |
rs558141786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406134 | CTGACAGGAGGTAAC[A/G]TGGTGTCTCAGCTCA | 11059 |
rs558150216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86380481 | TGAATATAGTGAAAC[C/G]ATTGAATTGTACAGT | 11059 |
rs558183960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457702 | TAAATGCGGTTTTTG[G/T]TTTGAGTTCAATAAA | 11059 |
rs558248531 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86415439 | TCTGATTTTTAGTGC[A/G]TTTCAATGAGTTGCA | 11059 |
rs558268426 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86407269 | TCTTTTTTCGGTTTT[A/G]TCTGTTCAATCTTTC | 11059 |
rs558270158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450142 | TTCTTGTAAATTGCT[A/G]TGGCCTTTCAAATTT | 11059 |
rs558293068 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86442375 | CAAAAGTGTGGCATA[A/C]AAATAAGCATGTTAT | 11059 |
rs558304524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400267 | AACCCGGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 11059 |
rs558342017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393063 | AAGGTCAGATGTTTA[C/T]TAGTCATTCATACTT | 11059 |
rs558360186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442907 | ACCAAGAAAGTTTCC[C/G]TGGAGAGTGTAAAAA | 11059 |
rs558459177 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86450972 | ATCCCAGGACTTTGG[G/T]AGGCCGAGGTGGGTG | 11059 |
rs558493801 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86435891 | CTTAAATAGAGATGG[A/T]ATTTCGCCATGTTGC | 11059 |
rs558500381 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362037 | ATATATATACACACA[C/T]ATATATATACACACA | 11059 |
rs558515014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428674 | GTAGCTAGCAGGGAG[A/G]GAGTGGGCAGCCTAG | 11059 |
rs558523156 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464521 | GCAGTTGGAAATCCA[A/T]TTTTTTTTTCCCAAG | 11059 |
rs558523667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436772 | GACGTCTTATTCCCC[C/G]CCTAGTATTATAATG | 11059 |
rs558544314 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432622 | TTTTTTTGTTTTTTT[C/T]TTGAGACGGACTTTC | 11059 |
rs558562958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437492 | TACAGTTTGGGGAAA[C/G]CAGTAGGGGAGATAA | 11059 |
rs558579052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373510 | GTGAATTTTATTTTG[A/T]CTTGTCTGGATAGAG | 11059 |
rs558645440 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425513 | AGAGACTGTCAAGCA[C/T]TGGCATGAGTTACTG | 11059 |
rs558678827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445397 | CCATCTATTTATGTC[C/T]ATGTGTGCCCAATGC | 11059 |
rs558694869 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432688 | TGTCAGCTCACTGCA[A/G]CCTCCACCTCCTGGG | 11059 |
rs558699349 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351485 | CTGGGACTACAGTTA[C/T]GCACTAACATGCTCA | 11059 |
rs558732605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458673 | AACTTAGTGACTGGA[C/T]TTCTGGCTTACTTCT | 11059 |
rs558734439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86466541 | AAAGAAAATGGATTT[C/T]TTTTTTTTTTTAAAT | 11059 |
rs558776525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389825 | TGGGGCGGCTGGCGG[A/G]GTGGGGGCTGCCCCC | 11059 |
rs558786247 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466658 | AAATTTAGATTACTC[-/TA]AATACTTCTGGCAAA | 11059 |
rs558788247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451640 | GAAAAGTTTTGGAGG[C/T]AGCCTTAGAAAAGCA | 11059 |
rs558806676 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86391043 | TCATCCTTGATGGTA[-/TG]TGTTATTACAGCCAT | 11059 |
rs558824142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444777 | TGGATACAGCAAATA[C/T]AAACAAGGAATCATA | 11059 |
rs558861269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359909 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGCGCC | 11059 |
rs558870319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461136 | TTTGAACCAATTCAG[C/T]GTTATTTAATTTCTT | 11059 |
rs558870432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360977 | TTCAGGGTAATTAGG[C/T]TGAGGAATGTCAGGA | 11059 |
rs558876155 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412172 | GTAAGAGTGACCATG[A/G]TACTCCATATAATAT | 11059 |
rs558880334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394491 | TAGAGACTTCATTTC[A/G]TTTGGGGAGGTCAAC | 11059 |
rs558950617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413548 | TTTCGAAAGCTATGA[C/G]ACGTCAGTGGATTCT | 11059 |
rs558951181 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467556 | GAAAGTCATATACTA[C/G]ATCCAATACTATTTA | 11059 |
rs559000517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389422 | CACCCCCCTTAATCC[A/C]TTTAACCCTGAGTGG | 11059 |
rs559006919 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461636 | AATTTTCTTCTTCAG[A/G]CAGAAGCAGCTTACA | 11059 |
rs559035925 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86414181 | GAAATATTGGAAGAT[C/G]TTAAATGTAGTAAGA | 11059 |
rs559084495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461718 | TTATTTAAGCAGTTG[C/T]CAGAAGAAAAAAGTT | 11059 |
rs559093201 | snp | A/G/T | 6.60735e-05 | 0.00574743 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381514 | TTCCAGAAATGTTAC[A/G/T]CCACAGACTACATTG | 11059 |
rs559110007 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467080 | TTATTTATTGTTCCC[C/T]TGAAATGACTGACCA | 11059 |
rs559130828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375257 | TAGTAATTCTCTATT[A/T]GGTTATATCACCAAA | 11059 |
rs559149177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416941 | TGAAAGTACCTTCCT[C/T]CCTTGCTGCCCAAGG | 11059 |
rs559165464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368549 | GAGCTTCCAAAGTTA[C/T]TTTTCCAAAATGCAA | 11059 |
rs559173192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86442512 | TGGGCAGTGGAGTTC[C/T]TAAAGACTGTTGAGC | 11059 |
rs559206200 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86406318 | AAGAAAAATATATTC[A/T]GTTCCACTTTGTTCC | 11059 |
rs559252693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349372 | TACAGTATCATTTCT[A/G]CCTTATTATACTGGT | 11059 |
rs559279968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344138 | TAGAAATGATCATTT[C/T]TCATAAATGGTTAGT | 11059 |
rs559407282 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86371748 | ATTAGTTTTTTGTTT[C/T]GCAAATTTATTCCAG | 11059 |
rs559446364 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86364433 | ATTTTAATGTAAGAA[C/T]ATGTTTTGCTTACAT | 11059 |
rs559455905 | snp | C/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377146 | GCTGGAGTGCAGTGG[C/G/T]GTGATCTTGGCTCAC | 11059 |
rs559479300 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86357622 | CCCTGGCATTCTTGG[A/G]ATTTAGTATTCAGTG | 11059 |
rs559487272 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344379 | AAGTTTCTGCCTTCA[A/G]AGAGATGGTAATCTT | 11059 |
rs559496750 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86379074 | ACCATCATATACTGA[C/T]TTTTCCTTCTTCCAG | 11059 |
rs559532029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365259 | AAAATACATTTTTCT[C/T]ATAGAAATACTTCCT | 11059 |
rs559549096 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86400097 | GTACTTTGGGAGGCC[G/T]AAGCGGGCAGATCAT | 11059 |
rs559670200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86392847 | GCCTCTTTATTCTTT[C/T]GAAAATTTTTTTGTA | 11059 |
rs559680073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435289 | CTGTAATAGTCCCCA[A/T]TACTTGAGCTTCTTT | 11059 |
rs559756164 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86393276 | CACTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 11059 |
rs559766008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394152 | ATTGTTTGAGCAGTT[C/T]TTAAAAACGGCTTCA | 11059 |
rs559767014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428200 | AGAGCCAGTCTTGCA[C/G]TATGCTACCTATTCT | 11059 |
rs559794590 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86379816 | AGTTAATAGTACCTG[C/G]CAGGGATGTTAATGG | 11059 |
rs559795430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86387854 | TTATATAATTTTCTT[C/T]CATCTTCATAATGAA | 11059 |
rs559802357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389147 | AAACATATAAAGAAT[A/G]TGTGGTTTCTTTTTT | 11059 |
rs559815459 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403640 | CAAGGTTGGTGTTTG[C/G]GGAGATGTTTACCAA | 11059 |
rs559830706 | in-del | -/AC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458128 | TGAGACTGCTTTTGG[-/AC]ACAGTTTATAATTTT | 11059 |
rs559890261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389618 | ATTTCCCCCTTTTCT[A/G]TTCGACAAAACCCCC | 11059 |
rs559974702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352035 | CTAGCTAGCTAAAAT[A/C]TTCCTTTTTTTTTTT | 11059 |
rs559977020 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86422294 | AAATTGAAAACTAGT[C/G]TCTTAAACTCAGAAG | 11059 |
rs559977405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415063 | CCAAGGAGGCAGTTA[C/T]ATGTACAGTTCCAGA | 11059 |
rs560008573 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363238 | TGACTGGTTAATGTC[A/G]GGTTACTTTTTTGTA | 11059 |
rs560021379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451082 | AAATAAAATTTTTTT[A/T]AAAAATTAGCTGGGC | 11059 |
rs560055747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86401415 | AATTTAAAAAATTAG[C/T]TGGGCACTGTGATGC | 11059 |
rs560068531 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446233 | GTGATCCGCCAACCT[C/T]GGCCTCCCCAAGTGC | 11059 |
rs560070979 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | WWP1 | GRCh38.p7 | 8:86423881 | CCCTCCCGGACGGGG[C/T]GGCTGGCCGGGCGGG | 11059 |
rs560105115 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417083 | CCAGCTGCCAGGGGA[A/C/G]GAGAGAAGGGCACAC | 11059 |
rs560133647 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451207 | ACCGAGTGAGACCCT[A/G]TGTTATTAAAAAAAA | 11059 |
rs560148365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410384 | TTCCCTTGAGTTAGT[G/T]TAGCTAATTTCAAAC | 11059 |
rs560155221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430578 | CACTGCGCCCAACCC[C/T]TTATCATATTTTTAG | 11059 |
rs560183670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382436 | GGGGGTGGTGGCTCA[C/T]GCCTGTAATCCCAGT | 11059 |
rs560193764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86424060 | AGACGGGGCGGCTGC[C/T]GGGCGGAGGGGCTCC | 11059 |
rs560205822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444410 | AAGGATATTTAGTTT[C/G]GAGATAGGCATTTGG | 11059 |
rs560211576 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419473 | GGATAAAAGTAGATA[C/G]AACATACATACAACA | 11059 |
rs560237069 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413599 | CAAATAGTGGAGGCA[C/T]GAGTGGTGAAAATTT | 11059 |
rs560244052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86436319 | TTAAAATTAAATTGG[C/T]AGATACTGTATTCCA | 11059 |
rs560273605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430125 | AGGATTGCTTGAGCC[C/T]GGGAAGCAGAGGCTG | 11059 |
rs560288249 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451882 | TTCTGTCATACTTCC[C/G]TGCTCTTACAGCTGC | 11059 |
rs560323095 | snp | A/G | 0 | 0 | intron-variant | WWP1 | GRCh38.p7 | 8:86402643 | GAATTTAAAAATTAC[A/G]ATGCCTGAAATTTTT | 11059 |
rs560325029 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455124 | CTTAAGAAGATACAG[C/T]AGTCATTCTTTATGA | 11059 |
rs560352802 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348134 | AAAACCATACGTCAG[A/G]TGGTTTTTAAGTTAT | 11059 |
rs560364867 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86423764 | GACGGGGTGGCGGCC[A/G]GGCAGAGGGGCTCCT | 11059 |
rs560386076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439069 | GTTTTAAAGGCTGGA[C/T]GTGGTGGCTTACGCC | 11059 |
rs560389843 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86374889 | TAATTTAAAAAAAAA[A/T]TTTTTTAGAGACAGG | 11059 |
rs560440146 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | WWP1 | GRCh38.p7 | 8:86403733 | AATTTCTTTAATAAT[G/T]CTCCCCTTAAAAAAA | 11059 |
rs560459890 | snp | A/G | 1.72994e-05 | 0.00294099 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466764 | TTCATTTTATTGAAA[A/G]CATCTGATTTTGTTT | 11059 |
rs560475132 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467204 | TTTATAGAGCTCCAA[C/G]TGTATTAAACATGAC | 11059 |
rs560495282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368686 | TGTTTGCCTGATCAC[A/G]TTACACTGTCCTTAT | 11059 |
rs560528688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361200 | AGCAAGCTGTGCTTA[C/G]TTTGGATGAGAAATT | 11059 |
rs560558334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460900 | CTACAAGCTCCACCT[C/T]CCGGGTTCACGCCAT | 11059 |
rs560589651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400762 | ATATTCAGTAAAATC[A/G]ATTATCTGCTGCAAA | 11059 |
rs560603370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347006 | TATATTTTATTTTAT[C/T]TTATTTTATTTATTT | 11059 |
rs560615673 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392947 | TACTAATTTATATAC[A/G]CAAACGTAGCGTATG | 11059 |
rs560626308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401352 | ATCGCTTGAGGCCAG[A/G]AATTTGAGACCAGCC | 11059 |
rs560655523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402973 | AGTTTATTTTCCAAA[A/C]GTAAGCATTACTGTA | 11059 |
rs560681783 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86363003 | TAATTTAGCATTTAT[-/A]ATAGTACTCGATAAT | 11059 |
rs560693989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395753 | ATGAATTAGAATTGC[A/G]GAATTAGTAATAAGA | 11059 |
rs560704295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346483 | TATTCTTTTCTTTCA[A/G]GAAGCCTTTATCAAA | 11059 |
rs560751655 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363326 | TTTTAGGGAAAGCTG[G/T]TCTGCTGGTCTGCTT | 11059 |
rs560784273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359386 | TGCCTATGGGGATTG[C/G]TGCCATTACTCAGCT | 11059 |
rs560813507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429231 | GCCTTTTTTACTTAG[C/T]GAAGGATGCCCTCAC | 11059 |
rs560840876 | in-del | -/AAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451251 | AAAAAAAAAAAAAAA[-/AAA]GATACATGAAAGCTT | 11059 |
rs560859658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430055 | AATACAAATATTAGC[C/T]GGGTGTGGTGGCGCA | 11059 |
rs560883371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450399 | TGAGGAAAATATATT[A/C]ATCAAAAGATCATGC | 11059 |
rs560897512 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392552 | AAGTAAATTATGTCC[A/G]AAATGATTTATAATG | 11059 |
rs560898336 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455799 | AAGGAAATACAGAGG[C/T]CCTAGAAGAGCAAAG | 11059 |
rs560900718 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394602 | TAGTCAAGGTTTGTC[C/G]TGCTTCTTCCCCATC | 11059 |
rs560919921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451005 | TCACTTGAGCCCAGG[A/G]GTTCAAGACCAGCCT | 11059 |
rs560920977 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348564 | CACAGCACATACTGG[C/T]GTACCTACTATGTGC | 11059 |
rs560950847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350661 | TACCCTAAATTATTT[A/G]GGTAGTTAAAAAATA | 11059 |
rs561014255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86351415 | GTGATCATGGTTCAT[A/G]GCAGGCTTGACCTCG | 11059 |
rs561014262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344286 | ACCTTAAAATGTGAA[A/G]CTGCTGGTAAGATCT | 11059 |
rs561018965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389525 | ATTTTTCTTAGTACA[A/G]AACAAAATGGAGTCT | 11059 |
rs561026319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344753 | AAGGTAATCCTAGCA[C/G]AGAGGTATCTCTAAG | 11059 |
rs561075696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451969 | TAGTTAGGAAATCTT[C/T]GTGTTTTCCAATAAA | 11059 |
rs561115080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436245 | ACAAGTTGATTCTTG[C/T]TTTGACACAATACTT | 11059 |
rs561137540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389105 | TCATTAAATAAACAT[A/T]TATTGAGTTTTAGGA | 11059 |
rs561161880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452843 | TTCTAGCATTGGGTA[A/G]GAGTCTTAATTATGT | 11059 |
rs561208452 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467127 | TAAATTTTGAAGCAA[A/G]TGAGAGACTTTATTA | 11059 |
rs561237704 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397304 | CACTGATAACTTTCT[C/T]TTTTAGTTTTTATTT | 11059 |
rs561249164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417010 | TGGTAGCTACCAGGT[C/T]CCAAGCCTTGGACAC | 11059 |
rs561255140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460689 | AATAGTGGCCAGCCT[C/T]CGTGTTCTCATGAGG | 11059 |
rs561275810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410244 | AAATAACATAAGAAT[C/G]ATCTATCCAATAAAG | 11059 |
rs561281157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374771 | CTGGAGTACGGTGGC[A/G]CAAACATACCTCCTT | 11059 |
rs561282797 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395824 | ACCAATACAAAATTA[C/T]ATGCCCAACTAGTCT | 11059 |
rs561293280 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346379 | AGTGAGCCGAGATTG[C/T]GCCACTACACTCCAG | 11059 |
rs561301590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86361044 | ATCACATAGGCATTT[A/G]TGAGTTTGGATTTAT | 11059 |
rs561307973 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384051 | TTGGCTTGTAGATGG[A/G]CATCTTTTCCCTGTA | 11059 |
rs561317771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368010 | TGTTTCCTCAACTGC[A/G]TGCTTCTCTAACTAG | 11059 |
rs561348728 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425611 | TATTTAGGACAGTTT[A/G]TATGTATGGTTCTCC | 11059 |
rs561355148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466704 | AGTATACATATATCC[A/G]TTCAGCATTTCTATG | 11059 |
rs561371285 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86416473 | GCAGCAAGCAGTCTT[A/T]CTGCCAACCCCTGTT | 11059 |
rs561407181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368588 | ACTGAAACCATCAGG[A/G]TAAACTTTAAAGTAC | 11059 |
rs561419200 | snp | C/T | 0.000132802 | 0.0081476 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402178 | AGCTCCAAAACCACT[C/T]GCATCTGAGCCTGCC | 11059 |
rs561424539 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86459757 | AGCTTCATTACAGTC[A/G]GTGTTCCATGGCTTT | 11059 |
rs561477900 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86376076 | TCTATTTTTGAAACA[G/T]TTCTGATGAAGCTGA | 11059 |
rs561503581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402848 | CATTGATTTCTAAGT[A/G]AAAGTGAGTAATGAA | 11059 |
rs561506754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438947 | CAATGTACAAAATGT[A/G]GGATCTGATTTTGTT | 11059 |
rs561527298 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WWP1 | GRCh38.p7 | 8:86390318 | CACAGGCTGCAATCT[C/T]GGCACTTTGGGAGGC | 11059 |
rs561551334 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86407898 | ATAATACATTGTTAT[G/T]AACTAAAGTCCATAG | 11059 |
rs561561571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369519 | TCAGGGTACAGAGAA[A/G]GTTTCATGTAGTAAA | 11059 |
rs561569344 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468522 | CCATAAAAGAGTTAA[C/G]TATTAGAATTACAAA | 11059 |
rs561592727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432014 | ATAACCCCTTGAGGT[A/G]GATACTATTATTTTT | 11059 |
rs561660860 | in-del | -/TTT | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86416578 | ATTCTTCCACATTTC[-/TTT]TTTTTTTTTTAAGCA | 11059 |
rs561667352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437956 | AGGCGCCCACCACCA[C/T]GCCTGGCTAACTTTT | 11059 |
rs561701668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430857 | TTTATATATATATAT[C/T]TCCCTTATATATGTC | 11059 |
rs561728518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382809 | ACTTAAGTAGCTTGT[A/G]ACAGTTCACTAAAAA | 11059 |
rs561768509 | snp | C/T | 0.031825 | 0.122064 | intron-variant | WWP1 | GRCh38.p7 | 8:86424552 | CTCCGTCTGCAATCC[C/T]GGCACCTCGGGAGGC | 11059 |
rs561831751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390754 | GGAGCGGGAGGGAGA[A/G]GGAGAAGAATATGTG | 11059 |
rs561854980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424964 | ATGTGGGGTATTCTC[G/T]TCCTTTTCTGCTAAC | 11059 |
rs561890100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418522 | CTCACTTAGCAAACC[C/T]AAGAGAGCTGGATTC | 11059 |
rs561921329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461569 | GGAGCGACATTCTGT[A/G]GAGAGAGTTTTCTTC | 11059 |
rs561972990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362256 | TGCCTAGTTTCTTTG[A/G]TTATTGATCACCTTT | 11059 |
rs562007408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86381238 | CAGTGTTACTATGAA[A/G]TCTCAGTAAGACTCC | 11059 |
rs562046027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419378 | AGCTGAGATCACACC[A/G]CTGCAGTCCAGCTTG | 11059 |
rs562106420 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386151 | AGTATGCTTTGCTGG[A/G/T]TCTCCTGTACTGAAA | 11059 |
rs562116557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86433607 | ACCTGTGATATTCCC[C/T]GTCACAGTTGATAAC | 11059 |
rs562119862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447887 | TAGGAAGATTGAGGC[A/G]GGGTATGGTAATAGA | 11059 |
rs562131401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86455492 | CATGGGTACAATGTT[A/G]ATACTTTAAAAATCA | 11059 |
rs562161999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439802 | TATTGTTTAGCAAAA[C/T]ATTTTGATTAAATCT | 11059 |
rs562214930 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360720 | ATAAGATAGTCTCTG[C/T]CCTCAGGGATCTTAC | 11059 |
rs562224237 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341778 | GGGACATCTAGCCTC[A/C]GAGATAGAAGGAAAA | 11059 |
rs562234580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377486 | CTGTAAACCGAGGTT[C/T]TCTGCCCTAAGCCAA | 11059 |
rs562329810 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447654 | CTAAGGTAGTATTAA[C/T]AGCTTCAGTGGATTT | 11059 |
rs562369670 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360972 | CAGCATTCAGGGTAA[C/T]TAGGTTGAGGAATGT | 11059 |
rs562370796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434149 | ACAATGTTGTTACTC[A/T]CCATACAGCACAGAG | 11059 |
rs562390111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86395371 | TTCAAATAAAACTTT[A/G]TTTATGAAAAATAGG | 11059 |
rs562395449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386183 | CAACTTATCACTAAT[A/C]ATGTCCTTGGTATTT | 11059 |
rs562405564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426587 | TGGAACCAGCAAATA[A/G]TTGGTTAGACTCTCA | 11059 |
rs562422506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346204 | GAAGAGCAGTTAGCA[A/C]TATCAGATCATTCAT | 11059 |
rs562434173 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86377948 | TTCATTCTTTTCAAA[A/T]GTTTCAAAATTTATG | 11059 |
rs562455491 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86437111 | ATGGTCTATTTGATG[G/T]ATAGCACTGAGCCCA | 11059 |
rs562470990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394738 | CACATATACAAACAC[A/G]TGTAGATGGGAATTA | 11059 |
rs562507371 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86389728 | ACTTCCCAGACGGGG[C/T]GGCCGGGCAGAGGCG | 11059 |
rs562524154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349671 | TGGGAATACCTAGCA[C/T]TCTCCTTGGTTAGAA | 11059 |
rs562544880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437944 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 11059 |
rs562560333 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369039 | GATACATAGTAAGTG[G/T]TTAACAATTTTTTTA | 11059 |
rs562573674 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86424471 | CTGGGAGGTGGAGGT[C/T]GTAGCTAGCCGAGAT | 11059 |
rs562584932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86403776 | GACTAAAATACGGTT[C/T]CCCAAGTACTCACAG | 11059 |
rs562605660 | in-del | -/CAGTATTGAAGC | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367192 | CTTCAAAATTAGACT[-/CAGTATTGAAGC]CAGGACTTTGTCTTC | 11059 |
rs562621499 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467888 | TCTGTTAGTGTTTGA[A/G]TATCTTCATTCCTCT | 11059 |
rs562642925 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440290 | ATAACATGATTTTTT[A/T]TTCCTAAATTTTTTA | 11059 |
rs562662469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417854 | TTGAGAGCCTTGTTC[C/T]AGGCATGTGCAGCAG | 11059 |
rs562667039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86431862 | TCAAGAAAACCTACA[C/G]AAGTGAAACCTTAGT | 11059 |
rs562696499 | in-del | -/TC | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86393169 | GAGCTCTTATTTTTT[-/TC]TCTCAGTTAATCATT | 11059 |
rs562698352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424141 | GATGGGGCGGCCGGG[C/T]AGAGACACTCCTCAC | 11059 |
rs562722613 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467266 | TTACCTTGTTAATAT[C/T]ATCTAGGGGAAAAAG | 11059 |
rs562799696 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368712 | CTTATGTTCCATTGT[C/G/T]CACTATGCAAGCAGT | 11059 |
rs562806184 | in-del | -/CAGA | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86385292 | TCTGCAGTGTGTCTG[-/CAGA]TGTTCCTCATCTATT | 11059 |
rs562909382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397218 | TGAAATGTTCCATGA[C/T]TGCAAAAACTGCAGA | 11059 |
rs562923614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86439743 | CTTTTATTTTTCAAT[G/T]TTGTCCCTTATTTGT | 11059 |
rs562928991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454581 | TTTTAATCTGAAGAT[A/G]GACATCTTGCATCCT | 11059 |
rs562943959 | in-del | -/CT | 0.00835141 | 0.0640778 | intron-variant | WWP1 | GRCh38.p7 | 8:86362159 | GCATATATATATACA[-/CT]AGGCATATATATATA | 11059 |
rs562944150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390690 | GAGACCGTGGAAAGT[A/G]GGAGACGAGAGGGAG | 11059 |
rs562946647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86412224 | GGTGATCTGTTTTCC[A/G]GACCTCATACTGGAG | 11059 |
rs562960963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362845 | TTAGTATCTCAAAAG[C/T]ACCTCAGTGTTTAGA | 11059 |
rs562971521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86347017 | TTATTTTATTTTATT[C/T]ATTTATTTTTGAGAC | 11059 |
rs563166986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384293 | AAAAGGTAAATAAAT[G/T]TATTTGAAGAATTAA | 11059 |
rs563188098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86391267 | CCCAAAGCTTTTGCT[C/T]CTTTAATCCTCTAAT | 11059 |
rs563203341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385070 | ACAAAATAAGTAACC[C/T]AAGAAAAACATGACA | 11059 |
rs563230377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86463048 | GAATGATTTTCTTGA[A/C]GGAAAGCTTTTGGGC | 11059 |
rs563238754 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349006 | CTTAGGGCTCACAAG[A/T]GTACAAAACAGAAGC | 11059 |
rs563242842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349200 | CTAATTTTTGTATTA[A/G]TAGAGATGGGGTTTC | 11059 |
rs563278650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363661 | AAACAAATTAGCCGG[G/T]TGTGGGCACCTGTGG | 11059 |
rs563307262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349897 | AGATGGGCAGAGATC[A/G]ATTCCCTCTGCCCTT | 11059 |
rs563362895 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436294 | TCAAAGTTTTGATAA[C/T]GCTATCAAATTAAAA | 11059 |
rs563417647 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343495 | AGTGACCTTGCAGAT[A/T]TTACCAGTCCTTATC | 11059 |
rs563418658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419780 | ATCTATTTTAAGACA[A/G]TTTGTTGTGAAAATT | 11059 |
rs563424651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86404369 | TAGTTGTATGTTTTG[A/G]CATTTGGATGTATTC | 11059 |
rs563429029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86463834 | GGAAGGCCGAGGTGG[A/G]AGGATCGCTTGAGCT | 11059 |
rs563457457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413521 | ACCTGCGCCGTTGAC[A/G]TCAAAGAATACTTTC | 11059 |
rs563480766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86441619 | GCGTCAGTGGGCTGA[A/G]TCAGAGTTGTTTCCC | 11059 |
rs563497632 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354440 | TAAATGAACTTTCAG[-/T]TTTTTTTTTAGCTTT | 11059 |
rs563499348 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342396 | CCCAAATCTCAGCGG[A/C]GGCCCCGCCCCTTCC | 11059 |
rs563516016 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86406214 | AAATTTATGAAAAGA[C/G]GATAATATGCGACTA | 11059 |
rs563522519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364243 | TGCTTTGAGGGAGAG[A/T]AATAAATTTGTATTC | 11059 |
rs563530379 | in-del | -/AA | 0.368554 | 0.220102 | intron-variant | WWP1 | GRCh38.p7 | 8:86442843 | TAGAGAAGGCTTTTA[-/AA]AAAAAAAAAAAGGAT | 11059 |
rs563539225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386355 | TCAAGGCTGCAGTGA[A/C]CTATCATTGTGTCTG | 11059 |
rs563554333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379730 | ATACTACTTCTTTTC[A/G]AAGCTAACTTTCCAG | 11059 |
rs563554605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399125 | ATGTTGCAGCATATA[C/T]AGTGCTTTATTTTTT | 11059 |
rs563592888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86372938 | TCTTTCAGACTTACC[A/G]GATGACCTACTAACA | 11059 |
rs563640132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399935 | GATTCATTAATGTTC[A/G]TTCAACAGATAGTTA | 11059 |
rs563649340 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460692 | AGTGGCCAGCCTCCG[A/T]GTTCTCATGAGGATG | 11059 |
rs563683586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442431 | TAGTTTGGCCACATC[A/G]AAACTAGCAGGTAAC | 11059 |
rs563698748 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380191 | GAGTGGAGTACTGGT[A/G]CATGTTACAATATGG | 11059 |
rs563706270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392745 | GACAAATTTTGTTTT[A/G]TAAATTCACTTACTA | 11059 |
rs563720643 | in-del | -/TT | 0.00116347 | 0.0240911 | intron-variant | WWP1 | GRCh38.p7 | 8:86425333 | GGTAATATAGCACTC[-/TT]TATGCATTTGTAATT | 11059 |
rs563742451 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462595 | AAAATCGGCCAGAAA[A/G]CAGTATAGGGAAGGA | 11059 |
rs563782117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365520 | TATTGCAAGTACTCT[G/T]CAAATCACTGGAATG | 11059 |
rs563796071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387113 | ATTAAGTTTCAACAT[A/G]CAAATTTTGTGGGAT | 11059 |
rs563847776 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437366 | TGCTCATTATAGCTG[A/T]GTTCCTTTCCTACTG | 11059 |
rs563874543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462381 | AAACAAAGACCCCGA[A/G]GAAATTGTTTTTCAA | 11059 |
rs563905153 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86432606 | GTTCAATCGCAGTTC[A/T]TTTTTTTGTTTTTTT | 11059 |
rs563906923 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86421719 | GTCCCAGCTACTTGG[A/G]AGGCTGAGACAGGAG | 11059 |
rs563924796 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433548 | CAAGAGCTAGTCTCT[-/A]AAAAAAAAAAAAATT | 11059 |
rs563963338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86462944 | AGTAAAAATTACTAA[C/T]TTTATTAAATCTTGA | 11059 |
rs563992520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425025 | AAGGGAATAATTAAG[A/T]GGTTAAAAAAGTACT | 11059 |
rs563998205 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86354946 | ATTAACACCTTTTTT[A/T]AAAAAAACCCTCACA | 11059 |
rs564001698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465475 | AAAAAAAAATACAAA[A/G]GTTAGCTGGCCATGG | 11059 |
rs564002695 | snp | A/C | 0.0014503 | 0.0268895 | intron-variant | WWP1 | GRCh38.p7 | 8:86458060 | TTGAAACAAAGTACT[A/C]AACATATTTTCTAAT | 11059 |
rs564009232 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86410390 | TGAGTTAGTTTAGCT[A/G]ATTTCAAACTCATTG | 11059 |
rs564058555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86370194 | TTAAAGCTTGCACAT[A/G]TGGTATTTTATTATA | 11059 |
rs564085097 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380519 | GGTGAATTATATGAT[A/G]TGTGAATGATAGCTC | 11059 |
rs564148831 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408154 | CTACAGTGTGGGTAG[C/G]CTTTTCAGATTGGCT | 11059 |
rs564223578 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86385223 | AAATGTTTGATAGTC[A/G]GCACCTTGAATAGAA | 11059 |
rs564266105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412430 | ATGTGTATTCCATTC[A/G]GTAATTTCTTTGACC | 11059 |
rs564282156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86398137 | CTCCAAAATTTATAA[C/T]ATGCACAGAAGCAAT | 11059 |
rs564299733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419243 | GCCAATATGGTAAAA[A/C]CCTGTCTCTACTAAA | 11059 |
rs564303010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412892 | AGAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC | 11059 |
rs564309670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86386257 | TTTAACATAGGTGGA[A/G]TTATTATGGAGAGTG | 11059 |
rs564328397 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86454794 | TTCTCACATACTGCC[C/T]TGTATGTGGGAAGGC | 11059 |
rs564436232 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383050 | TGAGTTAAGAAAATA[C/T]AATTATGGATTATAA | 11059 |
rs564460016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413581 | AAGAAGAGGAGGAGT[G/T]AGCAAATAGTGGAGG | 11059 |
rs564519787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426810 | GAACATGGGCATTGG[C/T]TATAGAGCAGATTGC | 11059 |
rs564532749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414267 | TGTGTGTATGTAAGT[A/G]AAATCAGTAGATAAA | 11059 |
rs564536642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378018 | ATGCATTAGTATCTT[G/T]CTTTTCTCTTTACTT | 11059 |
rs564545529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86441397 | TACCCTTCAGGCAGT[A/G]TCAGTGATTGTGTTT | 11059 |
rs564549750 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467637 | ACATGTTACTTTGAG[A/C]TGCTAGGTATTTGTG | 11059 |
rs564556961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420216 | CTCAGACAGCACTCA[C/T]TCTAGACTAGAAGCT | 11059 |
rs564569688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414895 | CCCCCCCCCATCCCC[C/T]CACCCCCGCCCCTAA | 11059 |
rs564569865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86407078 | AAAGTAAGGCTTGGG[A/G]GATGTTCATTCAGAA | 11059 |
rs564580221 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86434158 | TTACTCTCCATACAG[A/C]ACAGAGACTGAATTT | 11059 |
rs564586799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392022 | AACAGACAATAAATT[C/T]TTTTGGCAGCCTTAA | 11059 |
rs564603237 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384633 | GGTTTAGTACTTGGA[A/C]TCTGAGTTTTAGTTG | 11059 |
rs564620130 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86364351 | GTTAAAATTGGCATT[-/A]AAAAGGGAATCTACA | 11059 |
rs564658014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407494 | CACTAGGTGCCAGTA[A/G]TATCTTACCTTCTCC | 11059 |
rs564675050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442436 | TGGCCACATCGAAAC[C/T]AGCAGGTAACTTAAA | 11059 |
rs564736440 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466129 | TACTCAGTGCTGTAC[C/T]TCACAAAACGAAATG | 11059 |
rs564764103 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341306 | TCATAACAGGAGAGA[G/T]AGAGCATGTGAGCAT | 11059 |
rs564789058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449691 | AGATATTGCCTCCTA[C/T]TGATGTCTTCTATGA | 11059 |
rs564805503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464672 | CAGTGCACGCCACTA[C/T]GCCTGGCTAATTTTT | 11059 |
rs564806952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86435312 | GCTTCTTTTGGCCCA[C/T]CATGTATGTATACCC | 11059 |
rs564820772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420781 | GGTATATATAATTAT[A/G]TAGCTATGAAGGTAT | 11059 |
rs564832482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350072 | CTCTTCCTTGGAGAG[A/G]TGTCATTATAGTGGA | 11059 |
rs564843469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436160 | GTTATAGGTAAAGGT[A/G]CTGAGACTGAGAGAC | 11059 |
rs564848281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400111 | CGAAGCGGGCAGATC[A/G]TGAGGTCAGGAGTTC | 11059 |
rs564888213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86392940 | AAAGTTCTACTAATT[C/T]ATATACACAAACGTA | 11059 |
rs564897474 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86457532 | ATATACATAATGTGT[C/G]TATACATAATAGATA | 11059 |
rs564909763 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369066 | TTTAAAACTAAGACT[A/G]TAATTAATAGTCAGA | 11059 |
rs564920949 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86445654 | TAGCACAATTTATTT[C/T]CCTCTGGATATCTAT | 11059 |
rs564932169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357893 | ACAATTTGGCTGTTA[A/C]AGTACCAGTGGGCTT | 11059 |
rs564932627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429210 | GCTCTGTTGTTGCAA[A/G]CCCTTGCCTTTTTTA | 11059 |
rs564934128 | snp | G/T | 0.000399281 | 0.0141238 | splice-donor-variant | WWP1 | GRCh38.p7 | 8:86458026 | ATTTGGTTTTGGCAG[G/T]TATTTGCTTTTATCT | 11059 |
rs564934366 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403557 | GTCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 11059 |
rs564969726 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366627 | ATCTAACAGAATTAT[A/G]TTTTTATAACAGGAT | 11059 |
rs564999793 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86374534 | AATTTAGTTATTTCT[A/C]GGAGGTTTCAGTTAA | 11059 |
rs565007135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444322 | GAATATTTAGGTTTG[A/G]CTTGTTAAGTTTGAA | 11059 |
rs565017363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394063 | CCTCTTGAGTTCTCG[G/T]CAATAATGAGTGATT | 11059 |
rs565018917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358458 | ATCTGTGTATCTTCA[C/T]TTAATACACATTTAT | 11059 |
rs565048505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400480 | AAAAGAGATGCCAAG[A/G]AATCATCTCTGAGGA | 11059 |
rs565071557 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86458980 | ATACATCCGTTCTTT[A/T]TAAGTCTATACCTTG | 11059 |
rs565074079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344663 | GCAAGGTAGGGATAA[A/G]AGGGTTAGTTTGTAG | 11059 |
rs565077043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86443348 | CAAAGTGCTCAGATT[A/G]CAAATGTGAGCCACC | 11059 |
rs565086546 | in-del | -/AC | 0.0209421 | 0.100162 | intron-variant | WWP1 | GRCh38.p7 | 8:86457547 | GTATACATAATAGAT[-/AC]ACACACACATTTAGA | 11059 |
rs565131231 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | WWP1 | GRCh38.p7 | 8:86421835 | CTCAAAAAAAAAAAA[A/T]TTTTTTTGAAAATAT | 11059 |
rs565148766 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86380041 | AAAACATACGTCCAC[-/A]AAAAAAGCCTGTGCA | 11059 |
rs565158814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459609 | AGCCTTTTGCATTCT[A/G]TACTATTACCTATTA | 11059 |
rs565159049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359564 | TAGGTAACATTTCCT[C/T]AACTTTCTTTCCAGA | 11059 |
rs565160038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388078 | ATTTAAATAGCCATA[C/G]ATGGCCGCTGGCTAC | 11059 |
rs565235313 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375208 | TTTTCCCCCTTTAGG[A/C]CGTATAATCAAAATA | 11059 |
rs565237426 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347578 | TGTGTTAAAATGGTA[A/G]TCTCACTGCAGTGGC | 11059 |
rs565250345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388898 | CCCATTTGCTAACAG[C/T]CAGTAGACTTCTCTT | 11059 |
rs565255173 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86423467 | TCTGTTTAACAAAGC[A/G]CATCTTGCACTGCCC | 11059 |
rs565303622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397492 | GCAATTTTGAAATGT[A/T]CAACACATTATTTAC | 11059 |
rs565339512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86447594 | TTTTAATGATTGACT[A/G]TGGAATCTAAACTGA | 11059 |
rs565379019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86373894 | TAGGGTTTTCTTTTA[A/T]TGGGATGGTAATAGG | 11059 |
rs565413177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367288 | ATGTTTGTTAATTGA[C/T]CCAGGCACATAGATA | 11059 |
rs565433389 | snp | A/T | 0.031825 | 0.122064 | intron-variant | WWP1 | GRCh38.p7 | 8:86408923 | TCAAAAAAAAAAAAA[A/T]TTTTTTTCTTCGGAT | 11059 |
rs565522130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409481 | CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 11059 |
rs565536623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405022 | CATCATTCTATTGGC[C/T]GGTTTACAGAGGCTT | 11059 |
rs565553594 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86441764 | TATATAAGGAATGGA[A/G]GATTGTGGCTAAGCA | 11059 |
rs565558716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355262 | ATGATATCCTGATGA[C/T]GAGCACAGTGTAGAA | 11059 |
rs565614855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445113 | TACTCTTTTTAAAAC[C/T]AGCTCTGTAGGGAAC | 11059 |
rs565623231 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342435 | AGGCCCCGCCCCTCC[C/T]TACTATTGGCTGTCC | 11059 |
rs565660589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86413010 | ATTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTT | 11059 |
rs565670767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86455963 | TAGATCCACACCTAC[A/G]TTGTCAATTGATTTT | 11059 |
rs565687852 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452182 | GTTAAATGACTAGCT[A/G]TTCCTTCCCGGTGGG | 11059 |
rs565692124 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398058 | AGAGTCATCTGTGGT[A/G]CCTTGAGCTGAAAAG | 11059 |
rs565696106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86363788 | TGACAGAGTGAGACT[A/C]CATCTCAAAAAAAAA | 11059 |
rs565705481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405776 | GCCCCAAGCAATCAT[C/T]CCACCTCAGCTTCCC | 11059 |
rs565724121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355921 | TATGTAGTGAAAAGA[G/T]CATTAGCTTTGAGCC | 11059 |
rs565745473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372092 | GCAGTGGCGCGATCT[C/T]GACTCACTGCAAGCT | 11059 |
rs565753288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86433828 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCA | 11059 |
rs565766223 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348177 | CATGGTTTTTAAGTT[A/T]TAAGGAAGAGTAGCA | 11059 |
rs565775917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86348553 | TACAGTTCACTCACA[A/G]CACATACTGGCGTAC | 11059 |
rs565817465 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454039 | GTAGGATTTAGCCTT[C/T]TGGCAAGTCTGACTA | 11059 |
rs565818678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86377619 | AACGCGGAAAAACTG[A/G]TGGAAAAAATCAAAC | 11059 |
rs565827915 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346089 | CTTCTAGTTTTTAAC[A/G]TTTTGTGATTCTCGA | 11059 |
rs565869032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365803 | CCTGTCTCTATTTAT[A/G]TATAAAAAGCTTTAA | 11059 |
rs565922029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434331 | TGGTTTTCGCTCCTC[C/G]TCATTCACCGTGTTC | 11059 |
rs565950562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464419 | TTTATTTTCATATCA[A/G]AGTGAATTAATATTT | 11059 |
rs566008862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426976 | GACCATCCTGGCCAA[C/T]GTGGTGAAACCCCCA | 11059 |
rs566035749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86378385 | TCTCTTCATGTGACT[C/G]TTACTTATTTCTTAA | 11059 |
rs566051636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393021 | AATGAGAAGTTTTAT[C/T]ATCAAAGCATTTCTT | 11059 |
rs566058469 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86420323 | GTATTTGGGGTTTAA[A/C/T]GATAAGAATGTAGAC | 11059 |
rs566074318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465603 | GTAGCCTAGGCGACA[A/C]AGCCAGACCCTGTCT | 11059 |
rs566088822 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373073 | CAGTTCTTAGTTTGT[-/T]TTTTTTTTTTTTGTA | 11059 |
rs566124780 | in-del | -/C | 0.0134861 | 0.0810011 | intron-variant | WWP1 | GRCh38.p7 | 8:86390719 | GACGGGAGAGGGGGA[-/C]GGGAGAGGGGGAGGG | 11059 |
rs566146341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421217 | GAATATCATGAGTGT[C/T]CCAGTGTAGGATATA | 11059 |
rs566153532 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461026 | ATGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 11059 |
rs566179792 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86388258 | GTACCAGGTTGTCTG[G/T]TTTTTTTTTCCTTTT | 11059 |
rs566181417 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86414408 | CTGAAGTGAGGTAAA[C/T]GCTAATATTTTAGGT | 11059 |
rs566231420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450542 | TCAAAAACAGTCTAA[A/G]TAAAATTTCACTATG | 11059 |
rs566250663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86350754 | TGATAGCTGTTCAGT[A/G]TACTCATAAATCTGA | 11059 |
rs566259546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407191 | ATTTTAATTTTTTGC[C/T]CCGTGTTTCTGCATG | 11059 |
rs566267038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400839 | GATAAAGGTGTGGCT[A/G]ATTTTCAAAAGATTT | 11059 |
rs566272414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421919 | ATTTTGCAGATGGGG[A/G]AGGGAGGTAGAAGGA | 11059 |
rs566290298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86435090 | TTTAGGTTAGGCTTA[A/G]GATGTGGTAGAATTT | 11059 |
rs566295875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400256 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 11059 |
rs566299388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86449967 | CCAGTTTGGGCCACT[A/G]CAAACAAGACAGCAG | 11059 |
rs566311303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415407 | TGCCTTATCTCATCT[C/T]TTCATCTCTTCATCC | 11059 |
rs566336244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86442856 | TAAAAAAAAAAAAAA[A/G]GATAAGCATTATATT | 11059 |
rs566337764 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443686 | TCTGAAGGAAAGAGT[A/G]TGTTGCTTTTTTTAT | 11059 |
rs566396589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415939 | AGGCACTCAATAAAT[A/G]TTTGTTAAATAAGTG | 11059 |
rs566403622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443479 | ACTATTGTCTTTTGG[A/G]AAGTGTTTGTATTTA | 11059 |
rs566437235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409037 | GGTTTTTAAAAAAAT[G/T]TTCTTGTGTATTCTA | 11059 |
rs566491017 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383431 | TCGAAATGAAGCCCT[C/T]ACGAATTGTATAAGC | 11059 |
rs566516839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428521 | GCAGATAGAAAGGAA[A/G]TAGGAAAGAGACATA | 11059 |
rs566518525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381151 | AATTTTGGCATTTCA[A/T]AATAATAATGGCATA | 11059 |
rs566529882 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86422810 | ATAGAATAGGAAAAA[G/T]ATAAAAACGTCATTT | 11059 |
rs566551253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444726 | GTAGGGTGGAAAGAC[G/T]GATGGGAGTAAAATC | 11059 |
rs566672727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437251 | AAAGCCTACTTACTA[A/G]TAACCTTGATGTAAG | 11059 |
rs566680785 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86366619 | AATGAAAAATCTAAC[A/C]GAATTATATTTTTAT | 11059 |
rs566706217 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362047 | ACACACATATATATA[C/T]ACACATATATACACA | 11059 |
rs566708657 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438000 | AGAGACGGGGTTTCA[A/C/T]CATGTTAGCCAGGAT | 11059 |
rs566761227 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86356070 | TAATGTTAGAGATAA[-/T]TTTTTTTGTAAAGTG | 11059 |
rs566768934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367632 | AACATAATCAGCTTA[A/G]ATATTACTGACCATA | 11059 |
rs566777519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86452006 | GGTAAAGAACCTGTT[C/T]TCCAGCCTTAAGCCC | 11059 |
rs566786395 | snp | C/T | 0.000230335 | 0.0107291 | intron-variant | WWP1 | GRCh38.p7 | 8:86402233 | TTATGACACCTTGTT[C/T]AAAGGAAAAGTAAAT | 11059 |
rs566795874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451598 | TTGGAGTTGAGGATA[C/T]GGGACAAAGAGGGTT | 11059 |
rs566812599 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391529 | AAAAAAAATCCCTCT[A/G]TTGTTACAGATAAAC | 11059 |
rs566821477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438760 | ACATATGTGAATATA[C/T]TGTATTAAATTTTTG | 11059 |
rs566857314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345534 | CCTGCCTCAGTCTCC[C/T]GAATAGCTTGAACTA | 11059 |
rs566873676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400203 | CAGGCATGGTGGTGC[A/G]CACCTGTAATCCCAG | 11059 |
rs566905983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86394416 | GTTTTTTAAGCACCT[A/G]CCTTCTCTCAGTTGC | 11059 |
rs566947022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344999 | GTTTCAGAAGGATTA[G/T]TGGGATAGAGGTCTG | 11059 |
rs566983403 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366980 | TTGGAGTTGCTCTAT[G/T]GAGGGGGGAGACTGC | 11059 |
rs567014984 | in-del | -/TAAACTA | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86458495 | CGTGTGTGTTTTGCT[-/TAAACTA]TAATAGGATGGTCTC | 11059 |
rs567028010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389806 | CCCCCACCTCCCTCC[A/C]AGATGGGGCGGCTGG | 11059 |
rs567036354 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341530 | GTCAAGAGATACTTG[C/T]TGAATTCTGTACACA | 11059 |
rs567061993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427526 | TAGTTCATAGTTTTA[C/T]ATGTTTTAGTTATTT | 11059 |
rs567099843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86421554 | AATAGGCCGGGCATG[A/G]TGGCTCACGCCTGTA | 11059 |
rs567103807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392371 | TTTCAATTTTGAGGC[A/G]GAGAGAACCACTTTA | 11059 |
rs567113542 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WWP1 | GRCh38.p7 | 8:86390100 | ACATCCCAGACGGAG[C/G]GGCGGGGCAGAGGCG | 11059 |
rs567141449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375180 | TCATTGCAGTTTAAG[A/G]TTTCTTTGTGTGTTT | 11059 |
rs567145605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364128 | TACTCAAAAATGTAC[G/T]TGATTAGAATTAATG | 11059 |
rs567185660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421875 | ATATTAACAAATAAT[C/T]GGGAAAAGCTATTTG | 11059 |
rs567188276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386212 | TTTCAATAATTATAC[A/G]TTTGTTTAGTGTGTT | 11059 |
rs567243334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350197 | GATTCATTGATTGCT[A/G]TCTGGGTTTTTCTCG | 11059 |
rs567272078 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442727 | TCCAGCATCAACCAT[C/T]AATCCAGACCATCTT | 11059 |
rs567287437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458617 | TCCAAATCAGGGATA[C/T]TCTTCAGATAACTAC | 11059 |
rs567291134 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454428 | CTGAACCTGACTGAC[A/T]TAGACTGTCACTAAT | 11059 |
rs567305625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434989 | TTCTCTCACTGACCA[C/T]GTGAACCGTGTGATC | 11059 |
rs567313094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388195 | CTTTCCTTTCCTTCC[C/T]ACTTACTTTTATATT | 11059 |
rs567318222 | in-del | -/ATTGC | 0.00716266 | 0.059414 | intron-variant | WWP1 | GRCh38.p7 | 8:86421774 | CTTACATGAGCCAAG[-/ATTGC]ATTGCGCCACTGCAT | 11059 |
rs567331989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387507 | TTTATTTATTTATTT[A/G]TTTTATCATTATTAT | 11059 |
rs567410815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451367 | AGTGGCTATAGTGGC[A/G]CCTACAGTGATAGCT | 11059 |
rs567418736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351167 | AATGTTTATAAAGCA[C/G]AAAGCATGGTGGCTA | 11059 |
rs567431039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351684 | AATCTGGGATACTGA[C/T]TTAACATGGCTGGCA | 11059 |
rs567451666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444610 | AAGTGTGTTTCAAGA[A/G]GGAAGACATGGTCAA | 11059 |
rs567458016 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421988 | CCTCTTGGTGCAGGA[C/G]AACTTATCAAAACTC | 11059 |
rs567458961 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421995 | GTGCAGGACAACTTA[C/T]CAAAACTCACCATTC | 11059 |
rs567474233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86380233 | AAATGTAATGCTGAG[G/T]GAAAGAAGCCAGTCA | 11059 |
rs567530538 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447978 | GATTGTTTTAACTTT[A/G]TTTTTCATACCTAGC | 11059 |
rs567537081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445214 | AATTTTAGAATCAGG[A/G]GTACATGTGCAGGTT | 11059 |
rs567540151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415896 | ATTTCTATATTCTTC[A/G]TGCTCAAAACTATGC | 11059 |
rs567552887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415316 | TGAAAATTTACAAAT[A/G]TACAGAAAATTATAA | 11059 |
rs567554455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459007 | CTTGGAGTCATTCTT[A/T]TTCTTTTTCTTTTTT | 11059 |
rs567590265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86408991 | TTCATTTTGCTGAAA[C/T]GTTTTAGCTCCAATT | 11059 |
rs567604947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345470 | GCTGGAGTGCAGTGG[C/T]GCCTTCTGGGCTCAT | 11059 |
rs567667246 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86358849 | CATTGGGCTAGAGGC[G/T]GGAATTACAATGAAG | 11059 |
rs567699943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401167 | ATATTTAGCTTTTTT[C/T]GATCATCCTGTAGTC | 11059 |
rs567784486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401794 | GAACTGAAAAGTAAT[G/T]AAAACTTTAATATAA | 11059 |
rs567793203 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402621 | TTAATCTTCTAGTCT[A/G]TGATAGGAATTTAAA | 11059 |
rs567807196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375597 | TTATTCTGGAGTTTG[C/T]TTCATAACAGAATAT | 11059 |
rs567809168 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368390 | ATGAAGTGGGAAATT[G/T]TAGTTTTTCAGATTC | 11059 |
rs567812702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394322 | AGGAAGAAGGTCTAG[A/G]AGGTACAAAAAAATC | 11059 |
rs567814350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86437153 | AAGGAGGCATGCTGG[A/T]GAGCTGTGCTCCAAC | 11059 |
rs567841200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389770 | ACCTCCCGGATGGGG[C/T]GGCTGCCCGGCGGAG | 11059 |
rs567889456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389338 | TCCCTGGGTACTTGA[G/T]ATTAGGGAGTGTGAT | 11059 |
rs567927690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86381282 | TGGCTTGCTGATTCC[A/G]AAAATCCTCATCTAG | 11059 |
rs567989435 | snp | A/C/G | 0.00358891 | 0.0422285 | intron-variant | WWP1 | GRCh38.p7 | 8:86356725 | TTGTCTTTTCTTTCT[A/C/G]ATGTTTTCTAGTAAA | 11059 |
rs568035431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86395992 | CAAATCACCAAATTC[C/T]AGACACTTGAAATCA | 11059 |
rs568038881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86423880 | TCCCTCCCGGACGGG[A/G]CGGCTGGCCGGGCGG | 11059 |
rs568084293 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466949 | CCCCAGCCAAGAAAA[A/G]TTGCACAGATAGTGT | 11059 |
rs568124910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460389 | TTAGTTCTGCCACTT[C/T]AGCAGTTTGGGAAGG | 11059 |
rs568125888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416819 | ATTATCTGGTCTCTG[A/G]CCAAATCCAGCCCAC | 11059 |
rs568152017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410540 | TTTGTTAAAAATGCA[C/G]ATCCCCAGGTTCTTC | 11059 |
rs568157587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410019 | GTTTTGAAAATAATC[A/G]TATGACGTTTATCCT | 11059 |
rs568164898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390462 | CTTCGGGAGGCCCAG[C/G]CTGGCAGATCACTCG | 11059 |
rs568199625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403210 | TGTTCCTCCCTGTGT[G/T]TGTCTATTTATGGAA | 11059 |
rs568257057 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352964 | TACTAAAAGTTAAGC[C/T]AGAAGTTATGATTCA | 11059 |
rs568259268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353294 | CCTCCTCAGTCCTGT[C/G]ACCAGCAGGATCCAA | 11059 |
rs568265436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453206 | AAGTCCCCCTTTTCC[C/T]CAGCCCCTGGCAACT | 11059 |
rs568276961 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355348 | TTTCTGAGTAATTCT[C/G]TTAATCACCTCTCAT | 11059 |
rs568294644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418176 | ACCAAATATTTAATC[A/G]ACAAATATTTATTAA | 11059 |
rs568294792 | snp | A/T | 3.36655e-05 | 0.00410264 | intron-variant | WWP1 | GRCh38.p7 | 8:86425215 | TTATTTTTGTATTTT[A/T]ATTAAAGGTGGGAAC | 11059 |
rs568350134 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86446059 | TGATCTCAGCTCACT[A/G]CAACCTCTGCCTCCT | 11059 |
rs568367753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403850 | AAGAGAAGAATAGAT[A/C]CAATTATGGTGAAAT | 11059 |
rs568376338 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86439216 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTTCCAGCT | 11059 |
rs568388954 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86446529 | TTGGACTTAGCCAGA[A/C]ATTTTTTTGTCAAGG | 11059 |
rs568427448 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370438 | TGTGTGCAGAAATGT[C/T]TCCATAAGATTCATA | 11059 |
rs568435973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347207 | TCCTCAGGCTGGCCT[C/T]GAACTCCTGGACTCG | 11059 |
rs568532534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86376377 | AGTTTGTGACTGGCC[C/T]GGCCAACATGGTGAA | 11059 |
rs568584331 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86432795 | GTATTTTCAGTAGAG[A/G]TGGGGTTTCGCCATG | 11059 |
rs568610819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384419 | AAAGTAATTAAAATT[A/T]GATTTTAATTTAAGT | 11059 |
rs568635667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462640 | TGAATGCAGGGAGAG[C/T]AGTTAGAAAATTGTT | 11059 |
rs568662395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412550 | CAGTATATACAGTAC[A/G]GTCAGAAAGTATATA | 11059 |
rs568700686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409155 | AAATATAATCAATAC[C/T]GAATTGGCTTGGTAA | 11059 |
rs568747964 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414461 | AGTTGTGGGGAGATA[C/G]AATAGAAAAAGAGTG | 11059 |
rs568762377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370538 | CTTCTGTAATTGTTC[G/T]TTGGACAAACTCTTG | 11059 |
rs568783415 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443231 | GCTCACACCACCATG[C/T]CAGCTAATTTTTTTG | 11059 |
rs568809234 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86411262 | AAAACACTGGTTATC[A/T]TAATGCTGGTTCCTC | 11059 |
rs568827051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402308 | GTCTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 11059 |
rs568833411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410419 | TGATATGAAATTGTA[C/T]GTGGTATTTCTAATG | 11059 |
rs568835388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362655 | AAAAGGAGGGTTTAA[A/G]TGAGGGAGGAGAAGG | 11059 |
rs568869897 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WWP1 | GRCh38.p7 | 8:86423829 | CCCCCCCCACCTCCC[A/G]GACGGGGCGGCGGCT | 11059 |
rs568872238 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389102 | TCTTCATTAAATAAA[C/T]ATTTATTGAGTTTTA | 11059 |
rs568907291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422984 | TTTAGATGGGTACTT[C/T]TGAAATTATAGCAAA | 11059 |
rs568909568 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444943 | ATTTATAAAGAAAAG[A/G]GGTTTGTTTGACTGT | 11059 |
rs568915461 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | WWP1 | GRCh38.p7 | 8:86466551 | GATTTTTTTTTTTTT[A/T]TAAATTTGTCTTTAT | 11059 |
rs568949996 | in-del | -/TAATT | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86384398 | GACAAATGAGTAAAA[-/TAATT]TAAAGTAATTAAAAT | 11059 |
rs568954656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416748 | AGAATTCTCATTAAT[C/T]AGTAATTTGGTAATT | 11059 |
rs568959886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367716 | AACCCTGCTTTCTAA[A/G]TTGCTGAACCTAAAT | 11059 |
rs568970936 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368297 | CATACAGCTCTTAAG[A/T]GGCAGAACTGGAAAT | 11059 |
rs569057520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86431318 | GTTTTTATATATATA[A/G]TATATATTATATATA | 11059 |
rs569162373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86445398 | CATCTATTTATGTCC[A/G]TGTGTGCCCAATGCT | 11059 |
rs569167116 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414995 | GAGAGTGATGAGAAA[C/G]TGTTCTGTATTTTGT | 11059 |
rs569184420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395107 | AGTCTACACTCTTGG[A/G]CGTACCATCAAACCA | 11059 |
rs569207999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345706 | GTAAGCCACCCTGCC[A/G]GGCCTACTGGGAGCT | 11059 |
rs569213849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86438096 | TGAGGCACCACACCC[A/G]GCCTGTATACTGTAT | 11059 |
rs569219223 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443368 | TGTGAGCCACCACTC[A/C]CAGCCTACTTTTCAA | 11059 |
rs569233193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86390144 | AGACGATGGGCAGCC[A/G]GGCAGACACGCTCCT | 11059 |
rs569276996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461662 | TTACATTGTGAATTT[A/C]TTTATTTTGTATCAT | 11059 |
rs569402056 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86390430 | GAGTGAGCGAGACTC[A/C]GTCTGCAATCCCGGC | 11059 |
rs569411109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354151 | ATCATATGTAAACTG[A/G]GAATAATATACCCAA | 11059 |
rs569437392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382978 | AAGGTTCTTTCTGCA[A/C]ATCCACATGTAACTT | 11059 |
rs569450695 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86355071 | TAGGTCTGTCCGACT[A/T]GAAAACTGTTCTCTG | 11059 |
rs569464990 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365576 | TTTACTCTGCAGCAC[A/G]CTTGTAAGTTATCAG | 11059 |
rs569477301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460523 | AAAACCAGTGGCACA[C/G]TATTTGGCAGGAACC | 11059 |
rs569559245 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86376296 | AAACTAGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 11059 |
rs569564772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86362521 | AGAAGAATCGGTGAC[A/G]AGCTTAGACATCATT | 11059 |
rs569583671 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374358 | TGGTGGGAGAATTTG[A/G]GCTTTTGAATAAGTA | 11059 |
rs569590871 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468649 | TCCAGTTCGTTTTCA[C/G]GGTGCTGGTCTCCCT | 11059 |
rs569604878 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369594 | AGTATTGTAAACTTT[C/T]AAGATTCTTCTCAAA | 11059 |
rs569645254 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427120 | GTGAGCCAAGATCAC[A/G]CCATTGCACTTCAGC | 11059 |
rs569649294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370477 | CTTGGAAGACTGACA[A/G]CTTGTTATTTGTTGG | 11059 |
rs569662714 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86429232 | CCTTTTTTACTTAGC[A/G]AAGGATGCCCTCACC | 11059 |
rs569679561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447443 | AGCTAATTTTTTGTA[A/T]TTTTAGTAAGGACGG | 11059 |
rs569717295 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395717 | AGCTGTAGAGAAAAA[-/C]CAGAGTATTTGCAAA | 11059 |
rs569768820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86440220 | TTATTTGCCTCAACT[A/G]TTTGGGTCTAAGTTT | 11059 |
rs569791431 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411379 | TCTCCATTTTATTTT[A/G]TGTTACATATTTTGA | 11059 |
rs569807784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371286 | CCAATGGACATCTGA[A/G]TATTTTTCAATTTTT | 11059 |
rs569825891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384743 | TGGTGGCTCACACCT[A/G]TAATCCTGGCACTGT | 11059 |
rs569840714 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86371847 | AAAATATTCACCCTT[G/T]TTTTCTTTTTTTGAA | 11059 |
rs569849258 | snp | A/G | 2.0995e-05 | 0.00323991 | intron-variant | WWP1 | GRCh38.p7 | 8:86448122 | TTTTGCAAATTTTAA[A/G]TAAAATTTTTCATTT | 11059 |
rs569885910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440861 | ACTGTTTGCAGTACT[G/T]CCCTACGTTTTGCTG | 11059 |
rs569905442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398242 | AATTCCTTCCAAATG[A/T]CAAGTACTGAATTAG | 11059 |
rs569908993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391716 | TTCAATGGAGGCTCA[G/T]TAGAGTCAGGAAAAT | 11059 |
rs570014941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86396191 | GCAACTTCCACCTCC[C/T]GAATTCAAGCAATTC | 11059 |
rs570064742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86413318 | TATCCTAGTCTCTCA[C/T]GTGCCAGTCACTGTG | 11059 |
rs570066858 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416724 | CAGTTATAAATTAGA[A/G]TTCTATTGAGAATTC | 11059 |
rs570067572 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467479 | AATACAATAGTTGAA[A/C]ATTTTTCTCTGTTAC | 11059 |
rs570127972 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468094 | ATATTAATGCTACTT[G/T]TAGCAAACTGGGCTT | 11059 |
rs570156789 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437154 | AGGAGGCATGCTGGT[A/G]AGCTGTGCTCCAACC | 11059 |
rs570227091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86353376 | AAATATGGTTGAAAT[A/C]AACATAGGTTGCTAT | 11059 |
rs570246163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86364723 | AGGCAGGAGGATAGC[A/G]GGAGTCCAATAGTTA | 11059 |
rs570268159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456933 | ACAAATATAATCTGT[A/G]GTGAAATCATTGATC | 11059 |
rs570284987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442061 | AAGTTAAAAGTGTTA[A/C]ATAGCAGCAGTGCTG | 11059 |
rs570295254 | in-del | -/TAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86435320 | GGCCCACCATGTATG[-/TAT]TATACCCTTCTCTCC | 11059 |
rs570341660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354022 | TTTTCCATTAACGTA[C/T]TGGCTATTTAGAGCT | 11059 |
rs570354599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86461431 | CTTCTGTGCTGTAGG[C/T]AGGGCTTCATTTAGA | 11059 |
rs570433524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86390479 | TGGCAGATCACTCGC[G/T]GTCAGGAGCTGGAGA | 11059 |
rs570456933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417390 | TCTAGTGCATTATAG[A/T]TCTAATAAAGTGCAT | 11059 |
rs570493648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410867 | TTATGTCTCCCTCTG[A/C]CATTTCCATTAGAAC | 11059 |
rs570495310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86430545 | CCCTCCCAAGGTGCT[A/G]AGATTACAGGCATGA | 11059 |
rs570523088 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86369575 | ACTGTTCCCCAGTTT[G/T]CACAGTATTGTAAAC | 11059 |
rs570530442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86418014 | ACAAGATAAAAGTGG[A/C]TGAAGAGGCTAGAGA | 11059 |
rs570545674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86403347 | GTTGCCCAGGCTAGA[A/G]GGCAGTGGCAGGATT | 11059 |
rs570548391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404073 | TCTCAAATCTGAAAT[C/G]CTCCAAAATCTGAAA | 11059 |
rs570557477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86384554 | GGTTCAAGACAGCCT[G/T]GAAGCAATTTAAAAA | 11059 |
rs570567420 | snp | C/T | 4.95536e-05 | 0.00497738 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411577 | CACCAACTGATAATG[C/T]GTCTGTCACGGGTAC | 11059 |
rs570578824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446621 | ATTTAAGTATTTAAT[C/G]CATCTTGAGTTAATT | 11059 |
rs570587984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396849 | AAGTGATGCGCCTGC[C/T]TCACCTCCCAAAATG | 11059 |
rs570648249 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347218 | GCCTCGAACTCCTGG[A/C]CTCGTGGCCCTCCCA | 11059 |
rs570729517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86347550 | TAGAGGTAAACTTGT[A/C]AGTTTTTTCCTTTGT | 11059 |
rs570740907 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86376297 | AACTAGGCCAGGCGC[C/G]GTGGCTCATGCCTGT | 11059 |
rs570743870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397650 | TATATAGAAGTCTAA[C/T]ATATCGTTTAATGCA | 11059 |
rs570744385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413101 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCA | 11059 |
rs570808598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440046 | AACTTTTCCAGAAAC[A/G]AAACACTGCCTATCA | 11059 |
rs570827089 | snp | A/T | 9.90949e-05 | 0.0070383 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425254 | GATCCTCATGGTAGA[A/T]CCTATTATGTGGATC | 11059 |
rs570827698 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86405855 | TTTCTAAATTCCAAA[C/G]AAAGTTATGAATTCT | 11059 |
rs570842976 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86432921 | CCCACAGTTCATTTT[C/T]ATTGCTCCCCTTTAC | 11059 |
rs570843469 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86376908 | AAAGTCACCTTAAAA[C/T]TACCAGTCTTACTGA | 11059 |
rs570865835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406446 | AGAAGTACATGATAT[C/G]ACAAGTTTATTATAT | 11059 |
rs570866952 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463414 | CAAGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC | 11059 |
rs570929500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86370686 | CATTTCTTCTTTGTC[A/G]TAAGGAGTTGGAAGA | 11059 |
rs570933940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426075 | AATGTTATTTTTATG[A/G]GATATTTCTCTTTTA | 11059 |
rs570964094 | snp | C/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409821 | GCTGTGATTGTGCCA[C/G/T]TGCACTCCAGTCTGG | 11059 |
rs570967650 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86441845 | CAGATTACTGTAAGC[A/C/T]TTTGAGTTTGGAACC | 11059 |
rs571019836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419477 | AAAAGTAGATACAAC[A/G]TACATACAACAAGAA | 11059 |
rs571053730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456199 | AAACATAAGAGAAAT[A/C]TTGATGTAGGCAGAA | 11059 |
rs571090617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86434869 | AAAGTTCTTTGTGCC[C/T]GTCAGGCCCTCAATC | 11059 |
rs571141937 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440463 | CACACTTGTTTTTCC[A/G]ATACTCAGACATTGC | 11059 |
rs571142827 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416440 | GAGGATTAACTCTGG[G/T]ATTGTAGTTATGACA | 11059 |
rs571156710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456864 | GTGTATATGTGTATA[C/T]ACTATATATCACAAA | 11059 |
rs571184174 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456186 | ATGTGAAAGTGAAAA[A/G]CATAAGAGAAATCTT | 11059 |
rs571196581 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391808 | AAGTAACGAAGTCAG[A/G/T]ATTCTGTCCTCCCAC | 11059 |
rs571206181 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464745 | GGGTCTTAAACTCTG[A/G]GCTCAAGCTGTCCTG | 11059 |
rs571214973 | in-del | -/AAAT | 0.0217408 | 0.101969 | intron-variant | WWP1 | GRCh38.p7 | 8:86451054 | CATCTCTACAAAAAT[-/AAAT]AAATAAATAAATAAA | 11059 |
rs571240452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449026 | TTTTTTTTTTGTAAA[G/T]ATAGGGTCTCACTGT | 11059 |
rs571245175 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342074 | TGCGTTAATTGTGCG[G/T]ACACGTATACTCGGT | 11059 |
rs571264529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399411 | TTTAAATTGGAATAA[A/C]ATAATAGAGCAAATA | 11059 |
rs571276231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465167 | TAGGCAAAATTGGAT[C/T]GCTCACTTGGATTAG | 11059 |
rs571286547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86356657 | GTCTTTTAAAGGTCC[A/G]TAGCTGCTTAGGTTA | 11059 |
rs571299112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392331 | TAACATACACATTAG[A/C]GTATATTCAGAACTT | 11059 |
rs571310638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86349455 | ATTTGGGGCCACCCA[G/T]GTAACAGATTACCAT | 11059 |
rs571315335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86465567 | CAGCCTGGGAGGTCG[A/C]GGTCGCAGTGAGCCG | 11059 |
rs571321023 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342639 | TTAGGGCGCGGCGCC[C/G]GCGACGCGGCCACGC | 11059 |
rs571321849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343714 | GTAGTGTCTGTTATA[A/G]TTTTGACATTTTTAC | 11059 |
rs571410785 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86393830 | CCCCTCCCACACTGC[A/G]TCAGAGATTATCTGT | 11059 |
rs571421721 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422212 | TCTCATGTCGCTTCC[A/G]AAACACTGCCTTCTC | 11059 |
rs571423912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420429 | TGGCTCATCTGTGGG[G/T]AGAGTTTACATAGTC | 11059 |
rs571432456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386667 | ATTAATAATTCCACA[A/C]ATGAAAATATAAACT | 11059 |
rs571444385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358597 | AAGTGATTGTCCTAC[C/T]TCAGCCTCTTGACTA | 11059 |
rs571456703 | in-del | -/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341270 | TGAGTGGGCACATAT[-/G]GGGGCACTGTGAAGA | 11059 |
rs571469208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86378508 | AGTTTAAAAATACTT[A/G]TATAACCTTAGAGTG | 11059 |
rs571488595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427390 | TATCCCAGAACTTAA[A/G]GTAAAATTAAAAAAA | 11059 |
rs571530433 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WWP1 | GRCh38.p7 | 8:86353911 | TTACAAGTGAATACC[G/T]AACAGAACGTATATA | 11059 |
rs571533216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86451956 | AGTTCTTCTATTCTA[A/G]TTAGGAAATCTTCGT | 11059 |
rs571585469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415251 | TGTCCAAATCAAGCC[A/G]GTTTCCCCACATTTC | 11059 |
rs571597063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351638 | CCTGGCCAAATAAAC[A/C]AAAAAAAAGTTGCTA | 11059 |
rs571626154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86365942 | AAGCCCAATGGGAGA[C/T]AGAAGTGAAAAGTGA | 11059 |
rs571646008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86450153 | TGCTATGGCCTTTCA[A/G]ATTTACCCCCTTAGT | 11059 |
rs571649975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366340 | TGGCATGGGGATGAT[A/G]GGTGATGGCATGGGC | 11059 |
rs571665687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414560 | ACTCCACATCATCTT[A/C]CCTCTTTGCTTAAAA | 11059 |
rs571731143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86439465 | CTCCCAAAGTACTGA[A/G]ATTACAGGTGTGAGG | 11059 |
rs571760198 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86393314 | CGGGTTGAAGCGATT[A/C]TCCTTGCCTCAACCT | 11059 |
rs571766517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401073 | TTCCACTGCCAATAA[A/G]ACTTAAAATGTTTGA | 11059 |
rs571798723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86440276 | TAGCTAGTTCCTCCA[C/T]AACATGATTTTTTAT | 11059 |
rs571800645 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340867 | TAAACTTGTTCATAC[A/T]TTTTTATTACTTTTA | 11059 |
rs571805800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444502 | TGAAGAAGTTGTTCA[A/G]GGACAATTATAGTCA | 11059 |
rs571810633 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378413 | AAGTTTATTACTAGA[-/T]TTTTTTGAAGGGATG | 11059 |
rs571815255 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341418 | ACAGATGTATATTTT[C/T]GAATGATCTTTGTGG | 11059 |
rs571831969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443914 | TAATAGGAGATGAGA[G/T]TGAGAGATGCTGTGT | 11059 |
rs571850205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344943 | GTGGTGGGGCTTCCA[C/T]AGATGATTTTGAATT | 11059 |
rs572005098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86432587 | CTCTTCCCTTTACCA[A/G]TGTGTTCAATCGCAG | 11059 |
rs572018409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86428854 | GTAATACATATAGCT[C/T]TGTTTTTGGTTGGAC | 11059 |
rs572020301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436448 | GTCCTTCTCTTCTCC[C/T]TCACAGTCACATTCC | 11059 |
rs572073582 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422668 | GTGAGCCACCACGCC[C/T]GGCCCACCAGTTTTT | 11059 |
rs572077981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86363616 | AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCG | 11059 |
rs572107441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376554 | AGCCTGGGGGATAAA[G/T]TGAGGCTCTGTCTCA | 11059 |
rs572143222 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449840 | TACTTTTTTTTGTCT[G/T]AAGGACAGTACAGTT | 11059 |
rs572182731 | in-del | -/TG | 0.486153 | 0.0820481 | intron-variant | WWP1 | GRCh38.p7 | 8:86414231 | GTTTGTTTTTCTGTG[-/TG]TGTGTGTGTGTGTGT | 11059 |
rs572193809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400266 | GAACCCGGGAGGCGG[A/G]GGTTGCAGTGAGCTG | 11059 |
rs572231915 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86462923 | CGTTGAAGTTCTTTA[C/T]GAAGCAGTAAAAATT | 11059 |
rs572281464 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365787 | GGGCAAATAGTGAGA[C/G]CCTGTCTCTATTTAT | 11059 |
rs572287704 | in-del | -/AT/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401863 | ATTTTACTTGAAACA[-/AT/T]TAAAAACTCAATTGT | 11059 |
rs572302443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86391956 | GTAAGCCGTTTTTAG[C/T]AAATGCTCTAAGAAA | 11059 |
rs572321893 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432805 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 11059 |
rs572324926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419147 | GACTAGGGCTGGGCG[C/T]GGTGGCTCCCGTCTG | 11059 |
rs572331560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405284 | TGCTTTTAATCTCTT[A/G]ATCTGCAGTTCCACA | 11059 |
rs572337174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392586 | AAATCTCTCTTTATA[C/T]TGAATGGTGGGGAAA | 11059 |
rs572344931 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392313 | CCATAGAAATAGTAT[A/G]GCTAACATACACATT | 11059 |
rs572387936 | in-del | -/TTAAAT | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466641 | TTTTATATGTAAGTC[-/TTAAAT]TTAGATTACTCTAAA | 11059 |
rs572403940 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453405 | ATACTCCATTATAGA[A/G]TATTATGTACACTAC | 11059 |
rs572412937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412764 | GTCTGATGTTGTCCA[C/G]TGCTTAATTACGGTT | 11059 |
rs572413035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419682 | TAACAAAATAACAAA[A/C]ACAAATTTCTTTATT | 11059 |
rs572414073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86456441 | ATGGACAAAGGCTTA[C/T]TTCCCAATAGGATAT | 11059 |
rs572414322 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446245 | CCTCGGCCTCCCCAA[G/T]TGCTGGGATTACAGG | 11059 |
rs572424794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86386799 | AAAATACCTGAGACT[A/G]GGTAACTTATGGAGA | 11059 |
rs572431410 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425129 | TCTTTTAATGTAAAG[C/G]TTATCTGTAATTTTT | 11059 |
rs572497840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86356292 | TTATATGTTAACTTA[C/T]GTTGATTCTGTAAGT | 11059 |
rs572509825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86398869 | GTATACATTTTAGTC[A/G]TTTTTAATATATTAA | 11059 |
rs572536620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86404900 | TTTATAGGATCTCAA[A/T]GCTATGCTGTTCATC | 11059 |
rs572574306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86421590 | AGCACTTTGGGAGGC[C/T]GAGGCGGAAGGATCA | 11059 |
rs572609112 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WWP1 | GRCh38.p7 | 8:86441308 | GGTTCAACTACTACT[A/G]TGTTACAACTGGACT | 11059 |
rs572686035 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455932 | CAAATTGGTGGAACA[-/C]TAGAATGTCCAGAAG | 11059 |
rs572706296 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342244 | TTGCAATGTGTTCGA[A/G]GTCACCCAGCTAGGT | 11059 |
rs572749206 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | WWP1 | GRCh38.p7 | 8:86360651 | CAGTAACTATTAATT[-/G]GGGGGCCTTTCCCCA | 11059 |
rs572759785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86378782 | AGGGTATTCAGTGGA[C/T]GTATTTTGGATGGAT | 11059 |
rs572770429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343328 | CTGACTTTCACCCCA[A/G]TTTCAGCGTTGCAAA | 11059 |
rs572834647 | in-del | -/GGAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465421 | CAGTAGAAATGATGA[-/GGAG]GGAGGAGCCTGGGCA | 11059 |
rs572838739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86444214 | ACAGTTTTCTGACAG[A/T]TTAGATGCAGGGGTG | 11059 |
rs572845293 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86372317 | GTGAGCCACCGCGCC[C/T]GGCCTAATTTTTGTA | 11059 |
rs572956488 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86412920 | TGCAACTTCCGCCTC[A/C]CAGGTTCAAGTGAGT | 11059 |
rs572986974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86407411 | TTGGCCCAGGTAATT[A/C]TTTGTTGTAGGGGGC | 11059 |
rs573001714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86450243 | TTTTTCTGCTAAACC[A/G]GTCATCTCTGAGTGA | 11059 |
rs573046420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350485 | GCATCCTAATGCAAA[C/T]CTCTTTGCAAATTTC | 11059 |
rs573071445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351211 | TAAATCATGTTTATT[A/G]CTCGTAATTCAGTAT | 11059 |
rs573131283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466644 | TATATGTAAGTCTTA[A/G]ATTTAGATTACTCTA | 11059 |
rs573171382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359101 | GGTGATTCTGCCATG[C/T]AGCCAGATTGGGGAC | 11059 |
rs573192257 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466999 | TACAGTGAATTTTCC[A/G]AACCTCTCAAAGTAT | 11059 |
rs573266648 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388104 | GCTACTGTATTGGTC[A/T]GTGCAGTATCAGACT | 11059 |
rs573292004 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360426 | TGAAGTTTTCTTTTG[A/G]TTTTCCTCACCCCTT | 11059 |
rs573300658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429849 | TTTTAAATCATTTTC[A/G]AAAAACTAATAATTA | 11059 |
rs573308365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86388850 | TTCTGCAGTCTTTTA[A/T]ATCAGACCTGAGTTG | 11059 |
rs573309707 | snp | A/G | 4.97963e-05 | 0.00498955 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380808 | AGATGGAGAAATTAC[A/G]AAAACAGCAAAATCC | 11059 |
rs573315469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426507 | AGTAGAATTCTGGTT[G/T]GTAGAGAAATAGGGA | 11059 |
rs573332445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86422424 | CTGGAGTGCGGTGCA[A/G]TCTTGGCTCACTGCA | 11059 |
rs573353971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86419790 | AGACAATTTGTTGTG[A/G]AAATTTTAGTACATT | 11059 |
rs573355527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86358181 | TACTTTTGTATTGGA[C/T]GTTTTTCTATTGAGC | 11059 |
rs573404550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86374633 | GATATTTCCAATTCA[C/T]AATAATAACTGTAGT | 11059 |
rs573441690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86420507 | TGGTTGGGAGGAGGG[C/T]AAGTGTAGATGTGTA | 11059 |
rs573444888 | in-del | -/TATTT | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86346993 | GTAATAACTGCTTTA[-/TATTT]TATTTTATTTTATTT | 11059 |
rs573513197 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418990 | ACTCTTTAATTAATC[C/T]ACAATCCACAAGCCC | 11059 |
rs573545763 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441751 | ATAATTCAGCAGGTA[C/T]ATAAGGAATGGAGGA | 11059 |
rs573548484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416314 | AGAAGTGAGCAAGAG[A/G]ACATACAGAACTGAG | 11059 |
rs573569700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434439 | GGTATGCTCTTTTCC[C/T]GAAACTCCATATGGC | 11059 |
rs573573343 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415914 | CTCAAAACTATGCCT[A/G]CCGTATAGCAGGCAC | 11059 |
rs573577360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86457834 | ACATAATTTGCCATG[C/T]GCATAACTGCATTAG | 11059 |
rs573577423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86449547 | AAAATGTAAAAACTA[G/T]TCTTAGCTCAAATGC | 11059 |
rs573585301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416894 | GGAGACAAAGCCAGA[A/G]CAGCCCCCTTTACCC | 11059 |
rs573594134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86386740 | GTTACAGGGATTCAA[C/T]TTTTTCCGTAGATAC | 11059 |
rs573617971 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86349902 | GGCAGAGATCGATTC[C/G]CTCTGCCCTTGTGAT | 11059 |
rs573722324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395141 | TAAAATTAGGACGTA[C/T]CATCAAACCACTGGT | 11059 |
rs573730888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86350461 | ATGTACACTAAAAAA[C/T]GGGCCCCTGCATCCT | 11059 |
rs573731298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86464610 | AGCCTCAACCTCCTG[G/T]GTTCAAGCAATCCTC | 11059 |
rs573759055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86378597 | TATTCTACTAACTAG[A/G]ACAACTTTTTGAATT | 11059 |
rs573786413 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86365191 | AATTGGGTGATAACG[A/C/T]ATAGTAAGAATTGGG | 11059 |
rs573793193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WWP1 | GRCh38.p7 | 8:86465263 | CATAGCAACTCGAAA[A/G]CAGCAAAAGTTTTTG | 11059 |
rs573817652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86414662 | ACTATGGGTGCCTCA[A/G]TCCTGTTGATTGTAA | 11059 |
rs573843938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366000 | AACAATTGTACTTAG[C/T]CTGTTTTCTTGACAT | 11059 |
rs573847226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372224 | AGACGGGGTTTCACC[A/G]TGTTACCCAGGATGG | 11059 |
rs573882538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358146 | GTATTTAATAAGTCA[A/C]ACTAGCATTTTAGAT | 11059 |
rs573905549 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444656 | GATAGACTGAGCAAG[A/G]TGAAGCCTGGGATTT | 11059 |
rs573909802 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367107 | AGGTTCCACATTTAT[C/T]GAACTAAACTGCTCT | 11059 |
rs573960644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86394062 | CCCTCTTGAGTTCTC[A/G]GCAATAATGAGTGAT | 11059 |
rs573979998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86443181 | AGACTCAAACGATCC[G/T]CCCACCTCAGCCTCC | 11059 |
rs574065420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366961 | GAAATATTTATTTTA[C/T]GCTTTGGAGTTGCTC | 11059 |
rs574072598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435232 | ACAAAAGATCCAGCC[A/G]TAAATACAATGTCCT | 11059 |
rs574081560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86400412 | ATAGCGATAAGCACT[A/G]TGAAGTCATTTAAAC | 11059 |
rs574103148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86387806 | CGGGATTATAGGCAT[A/G]ACCCACTGCAACCCA | 11059 |
rs574117512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86393233 | TTTTTTTGAGACAGG[A/G]TCTCACTCTGTCTCT | 11059 |
rs574136869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86379745 | GAAGCTAACTTTCCA[A/G]ATAAAACATTAAAGC | 11059 |
rs574214446 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378987 | AAATTAATTGACTTA[C/G]TGTGGTCAGGCTTTT | 11059 |
rs574301336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86429058 | TGTCATCAAGGACCC[A/G]GGTTCTTTCTGCCCT | 11059 |
rs574316842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86415636 | ATCTTTATCGAGATA[C/T]AGAACATTAATATCA | 11059 |
rs574325364 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350887 | TGTGTTTAGTTAGAC[G/T]GGGGAGGAGAATTAG | 11059 |
rs574328398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395219 | AAGGGAACAAGCCAC[C/G]ATAAGCAGAGGTTGT | 11059 |
rs574328850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416224 | GGAAGTGTGATAGAG[A/G]ACTCTTTGGAAGCAT | 11059 |
rs574338132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86422235 | GCCTTCTCGAGTTCT[C/T]GTGTTTAAGAAAAAG | 11059 |
rs574349529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458797 | TGTGAGTTTATTGCT[C/T]GATATTTTAAAGAGA | 11059 |
rs574388492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86459463 | TTGGTTAAAAAGTTA[C/T]TGTCTGTATAGTAAG | 11059 |
rs574421278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86409300 | GTACAGTGGCGTGAT[C/G]CTGGCTCACTGCAAC | 11059 |
rs574441272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360159 | AAAAAAAAACAAAAA[A/G]CCAAACCAAACCAAT | 11059 |
rs574467679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86351962 | TTGAGAACTGTTGGT[A/G]GAAACTGAATTGGTT | 11059 |
rs574508905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424049 | CCTCACTTCCCAGAC[A/G]GGGCGGCTGCCGGGC | 11059 |
rs574535146 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462124 | TTTTTTATGAAGTTT[G/T]TGCCCCATGGTGGGG | 11059 |
rs574562042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86451761 | TGGCTTCTCTGTATG[A/G]GGTGGTGTATGCTGC | 11059 |
rs574579432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436898 | GAATTTCAAACCATA[A/G]CTTAATTTTACGATT | 11059 |
rs574633671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86417729 | AACTGTTTCTGATTA[C/T]AAAATTAAGACATGA | 11059 |
rs574700318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86382417 | AAAAACCAGGGTTCT[A/G]GCTGGGGGTGGTGGC | 11059 |
rs574705111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86453599 | CCTCTATTTAATTTT[C/T]TGAGGAACTACCATA | 11059 |
rs574718343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345251 | TTTACCCTCAGCATA[C/T]GTGTGCTACTTTACA | 11059 |
rs574778384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345802 | CTGTATATATACAGA[A/G]ACACAATATTACATT | 11059 |
rs574789106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446274 | GGCGTGAGCCACTGC[A/G]CCCAGCAGCTGCTTA | 11059 |
rs574794232 | snp | A/G | 0.00183037 | 0.0301966 | intron-variant | WWP1 | GRCh38.p7 | 8:86431526 | TAAGTCGTCTTGCAT[A/G]TATCAGTAGGTAGAA | 11059 |
rs574812375 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86346954 | TTGGTTCTCATGACA[A/C]CTGATAAGTTGGTGT | 11059 |
rs574864876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86434276 | AACAGCCTAAATGGC[C/T]TTACAGGATCTGACC | 11059 |
rs574914749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411121 | TCATACAGTTCCTAC[G/T]ATTGGCAAAACAGTT | 11059 |
rs574988448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86353523 | TCTGAGACGGAGTCT[C/T]ACTCTGTTGCCCAGG | 11059 |
rs574992761 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356588 | ACCATTTAGGTTTAT[C/G]TTTTGTTGACATAAT | 11059 |
rs575009630 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86461406 | GACTTGATTGAACCT[-/A]AAGATTACTCTTCTG | 11059 |
rs575043553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86411943 | ATACGATTATTGAAT[A/G]TGTGCATAAAATGTT | 11059 |
rs575051883 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383832 | ATAAAATTTAATAAA[C/T]ACTCATACAGTCAGT | 11059 |
rs575069451 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379687 | TATAATGACATTTTG[A/C]TTTTTAAGCTTTTAT | 11059 |
rs575076373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86454266 | AATGCTATGGTAAAT[A/G]GTTGTTATACTATAT | 11059 |
rs575085533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401302 | ACAATGGCTCACACC[C/T]ATAATCCCAGCACTT | 11059 |
rs575095594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86354255 | ACCTTCTCATTGATG[C/T]CAGATCTATTTCAGA | 11059 |
rs575122838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86401915 | TTTTAAAAAAGAAAT[A/G]ACAAAAAAGAAACTT | 11059 |
rs575140484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86372837 | AGAAGTAGCTCTGAC[G/T]TTGTTGATCCTTTCT | 11059 |
rs575163152 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WWP1 | GRCh38.p7 | 8:86414902 | CCATCCCCCCACCCC[C/T]GCCCCTAAATAGCGA | 11059 |
rs575187762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86436800 | ATGATGAACCAAATT[A/T]TGCTGTGTACTCAGG | 11059 |
rs575198482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86366128 | TGCTGGAGAGACTGT[A/G]GTTCCTGAGTTAAGC | 11059 |
rs575204716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362669 | AATGAGGGAGGAGAA[A/G]GGAGGGAAGGCATTA | 11059 |
rs575222063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86415527 | AATATGTTTTAAAAT[G/T]TTTTTAGATAAAGAT | 11059 |
rs575236340 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351215 | TCATGTTTATTGCTC[A/G]TAATTCAGTATTATG | 11059 |
rs575236658 | in-del | -/T | 0.24449 | 0.249939 | intron-variant | WWP1 | GRCh38.p7 | 8:86371041 | TGGCTAATTTTTGTA[-/T]TTTTTTTTTTTTTTT | 11059 |
rs575294865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86430530 | AATCCTCCCACCTTG[C/G]CCTCCCAAGGTGCTG | 11059 |
rs575362711 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86450982 | TTTGGGAGGCCGAGG[G/T]GGGTGGATCACTTGA | 11059 |
rs575391942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86458713 | TTTCATTTTCAGGTG[A/T]AGAGTAATGCTGGGT | 11059 |
rs575399891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86444352 | AGTAGACATCCACAT[A/G]GAGATGTAAAAGAGA | 11059 |
rs575400361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86358473 | TTTAATACACATTTA[G/T]TGAGGAGTTTTTTTT | 11059 |
rs575413526 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432727 | ATTCTCCTGCCTCAG[C/T]CCCCTGAGTAGCTGG | 11059 |
rs575421984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394066 | CTTGAGTTCTCGGCA[A/G]TAATGAGTGATTATT | 11059 |
rs575437489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86359342 | TGTTTCTAACCATGA[A/T]CTATTAAAATGAGCT | 11059 |
rs575460557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345104 | CTGAGCTGTGGTGCA[C/T]GCGAATGGAAAGGAA | 11059 |
rs575462608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86394514 | AGGTCAACCAAAAAA[C/G]AAAAACATTCTTTTA | 11059 |
rs575496652 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436219 | AAAATAAAGCTTAAA[C/T]AGCTTTTGGAACAAG | 11059 |
rs575507797 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WWP1 | GRCh38.p7 | 8:86388922 | TTCTCTTTTCTTATT[C/T]ATGACTTTTTGAAAT | 11059 |
rs575524284 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86359952 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 11059 |
rs575546739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351365 | TTGAGACAGGGTCTC[C/T]GACAGCTCTGTCTCC | 11059 |
rs575554251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86352733 | TAACATCTGAACCTT[C/T]CAGATGTTTAAAACA | 11059 |
rs575610142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86351817 | AATCCTTATATAACA[A/G]TCGTCTGGGATGCTT | 11059 |
rs575632400 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86389902 | CACCTCCTGGACGGG[G/T]CGGCTGCCGGGCGGA | 11059 |
rs575644738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86423628 | TGTCTACTTCTTTCT[A/G]CACAGACACAGCAAC | 11059 |
rs575666690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86353452 | TTTTCTCAATTTGAG[G/T]AGAAAGGATTAGTTT | 11059 |
rs575682399 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408060 | TTCATTTGTTTATCC[C/G]TCAAACCCTTTGCAA | 11059 |
rs575698433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86424035 | CGGGCGGAGACGCTC[C/T]TCACTTCCCAGACGG | 11059 |
rs575730636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86346815 | AGTTACTAATACTTA[A/G]TGGAGGAAAAATGAT | 11059 |
rs575735641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86416980 | GGTCACCACCACATT[C/T]TGGGGACTCACTTTT | 11059 |
rs575744957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86347226 | CTCCTGGACTCGTGG[C/T]CCTCCCACCATGGCC | 11059 |
rs575761005 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367951 | ATGGAAGTTAATACC[A/C]CTTACATAAACCGTG | 11059 |
rs575780834 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380244 | TGAGTGAAAGAAGCC[A/G]GTCACAAAAAAAACC | 11059 |
rs575838630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360982 | GGTAATTAGGTTGAG[G/T]AATGTCAGGAATAGA | 11059 |
rs575870521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375312 | TTTCAGTTTTTTTTT[A/T]AATTTTGTTTTATAA | 11059 |
rs575906047 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WWP1 | GRCh38.p7 | 8:86410967 | TTTTTATAGTGACAC[A/G]TAGTCGAACTAGATC | 11059 |
rs575912577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86376477 | GGGAGGCTTAGGCAT[C/G]AGAATCACTTGAACA | 11059 |
rs575919998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86361840 | CCCCTTTCTGTCAAT[A/G]AACTTAAAATTGAGT | 11059 |
rs575954197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446229 | TCAGGTGATCCGCCA[A/C]CCTCGGCCTCCCCAA | 11059 |
rs575971682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86410208 | TTTCACTTTTTCTCC[C/G]CTAATGTGTTATAAC | 11059 |
rs575974453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86396332 | TCTTGATCTCCAGAT[A/C]TTGTGATCCGCCCGC | 11059 |
rs575979841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86395419 | GAGGAGATATATTTT[A/G]AGAGAGAATGGCTGC | 11059 |
rs576002131 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369298 | TTATTAAATGAAGTG[C/T]GGAGAATAATTGTTG | 11059 |
rs576009820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402787 | CACAAAAAATACTAT[A/G]TAATTCATGATATAA | 11059 |
rs576038522 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398927 | TGATTTCAGAATATT[C/T]TACCTTGAAGAGAAA | 11059 |
rs576071722 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86390287 | TCCTCACTTCCCAGA[C/G]GGGGTGGCGGCTGGG | 11059 |
rs576078472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446923 | GCAGATATAGTAGAA[C/T]ACAAAAGTTTTCTTC | 11059 |
rs576123091 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423197 | TGTCAGAAAAAGGGT[A/T]ATTTTTATTTTTATT | 11059 |
rs576141141 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86405111 | ATCACTTAATAAAGG[A/G/T]TGAATTCAGGTATCT | 11059 |
rs576181456 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346400 | TACACTCCAGCCTGG[A/G]CAACAGAGCGAGACT | 11059 |
rs576217846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86405984 | ATATGAGGGCTTCCA[C/T]CTCCCCCACCTCCTG | 11059 |
rs576231155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86431893 | ATAGCTGTCTTTGCT[C/G]TCATTTGACAATGGA | 11059 |
rs576256023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86398853 | AATTCACTTTTTAAA[A/G]GTATACATTTTAGTC | 11059 |
rs576310069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86462174 | AACAAATAACTATTT[A/G]CAAATCCTGGGAAGT | 11059 |
rs576317326 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WWP1 | GRCh38.p7 | 8:86424477 | GGTGGAGGTTGTAGC[A/T]AGCCGAGATCACGCC | 11059 |
rs576334065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412349 | TGGTTAGTAATTCTT[A/G]ATCTCTTTTAAGTTT | 11059 |
rs576361472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86419126 | AAATACTGTTTTAAG[A/G]TATCAGACTAGGGCT | 11059 |
rs576362552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86362952 | TTGAAAATTGTTTCT[C/T]GTATTTAATATTATT | 11059 |
rs576400350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86460474 | CTAATGATTCTACCT[A/G]TCTCATAGAATTGTT | 11059 |
rs576402493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86360216 | TTCTCTTTGATAGTC[A/C]AAATCATCTGAAAAT | 11059 |
rs576444714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86425457 | TATATAAATAATGAA[A/T]GTTCAGTCAATGAGA | 11059 |
rs576446071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86412652 | CTAGATGTCTCTACA[C/G]TATTGTCTTCATTTT | 11059 |
rs576486080 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | WWP1 | GRCh38.p7 | 8:86364575 | TTTGGGAGTCTGGGG[-/T]TGGGAGGCTCACTTG | 11059 |
rs576576644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86356094 | TAAAGTGACTGACAT[A/G]TAATAGGAGCCCAGT | 11059 |
rs576582384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86455301 | CTCTTACCACTTCTA[C/T]TCAATATTTTACCAA | 11059 |
rs576583590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86389939 | CCTCACTTCCCGGAC[A/G]GGGCGGCTGCCAGGC | 11059 |
rs576595305 | in-del | -/AA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364833 | AGAAAGAAAGAAAGA[-/AA]GAGAGAGAGAGAGAG | 11059 |
rs576659441 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341763 | CAGTGGAGAGGAGCA[C/G]GGACATCTAGCCTCC | 11059 |
rs576674176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447821 | TTTCAGGTGCACAGG[A/G]CCCTTTTATATTTCC | 11059 |
rs576692166 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432199 | TGAAATGATTTTTCC[A/G]GATTTAAAGATACCT | 11059 |
rs576794915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86402628 | TCTAGTCTATGATAG[G/T]AATTTAAAAATTACA | 11059 |
rs576902840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86446198 | TGTTGGCCGGGCTGG[A/T]CTCGAACTCCTAACC | 11059 |
rs576914621 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394212 | GTGAAACATGTTTTC[A/G]ACAAATCCATGATTT | 11059 |
rs576916380 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371832 | AGTTTCCGTGTAGTC[A/G]AAATATTCACCCTTT | 11059 |
rs576992831 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369223 | CCTCACACAGTGTTA[C/T]TGTAATGCTCAGATG | 11059 |
rs577007164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86445474 | TTGGGAAAATGGCCT[C/T]CATCTGCATCTGTGT | 11059 |
rs577116753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86439682 | CTACATTCACTAAAT[A/G]TATTGTTAACAGTAG | 11059 |
rs577123842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86375862 | TCTCCATGGGGTCTG[C/T]ACCATTTTGTGTCTA | 11059 |
rs577172987 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400339 | CTTCGTCTCGGGGGG[-/A]AAAAAATAAATAAAT | 11059 |
rs577193587 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348506 | TACAGGCATGAGCCA[C/T]CACGCCTGGCCGTCT | 11059 |
rs577216418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369438 | ACATGTGCTCTTGAG[C/T]CTGGGGATTGGGTGA | 11059 |
rs577252865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86369881 | TACTGTATCTACTTC[C/T]GTGCCTTCCATACAT | 11059 |
rs577274451 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86448615 | CATGCCTTTGGGAAG[-/TTC]TTCTCACCAGTACCA | 11059 |
rs577277867 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467857 | TTTGAATGCTCTAAT[A/G]TAAGGCTAATGATTT | 11059 |
rs577318241 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423815 | CGGGCAGAGGCGCCC[-/C]CCCCCCACCTCCCGG | 11059 |
rs577341692 | in-del | -/AGTC | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86385219 | TAGAAAATGTTTGAT[-/AGTC]AGCACCTTGAATAGA | 11059 |
rs577386923 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378632 | AGGTTGTCTTCTAGT[C/T]ATTTAAAATCACATT | 11059 |
rs577395594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397105 | AGATAACTTGTGAAC[A/T]TATTTATGCTGGACA | 11059 |
rs577403432 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86362039 | ATATATACACACACA[C/T]ATATATACACACATA | 11059 |
rs577408308 | in-del | -/AGCCTTCTG | 0.0023933 | 0.0345097 | intron-variant | WWP1 | GRCh38.p7 | 8:86454033 | TCCTATGTAGGATTT[-/AGCCTTCTG]GCAAGTCTGACTAAC | 11059 |
rs577425106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86362514 | CAAGGGTAGAAGAAT[C/T]GGTGACAAGCTTAGA | 11059 |
rs577462292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86447679 | GGATTTTTTTAGTTC[C/T]CCAAAATTGGTGGGA | 11059 |
rs577482433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86397919 | TGTCTCCATTTTGTA[A/T]TTAAGAAACCAAGGC | 11059 |
rs577520692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86391164 | CTGCGTCTTGTTAGG[A/G]AGATTGTTCCACTTC | 11059 |
rs577542260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86356359 | TTCTTCAGAAACATG[C/T]AGTATAGGAGTGGGA | 11059 |
rs577560341 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416577 | ATTCTTCCACATTTC[-/T]TTTTTTTTTTTTTAA | 11059 |
rs577594583 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341547 | GAATTCTGTACACAC[C/T]CATGAAGTGTTGGGG | 11059 |
rs577611244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86355368 | TCACCTCTCATCCTC[A/C]GCTCAGCTCCATGAC | 11059 |
rs577626945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86357376 | TAACAGCCAAATACT[C/G]TTTTCATTTTGATGA | 11059 |
rs577628006 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86425720 | TAATGACTTAAAGGC[A/C]CAAAACTATGATCTA | 11059 |
rs577631561 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WWP1 | GRCh38.p7 | 8:86390658 | AGCACAGTCCAGCCT[C/T]GGCTCAGCATCAGAG | 11059 |
rs577716791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86426266 | ACTTGGGGTTTATTT[C/T]ACTGAAACTGTTGTC | 11059 |
rs577769468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86371457 | GAAAACGCCTACCAG[C/T]GGTGTATAAGAGCCA | 11059 |
rs577790185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86377325 | CTGGTCTCGAACTCC[C/T]GACCACAGGTGATCC | 11059 |
rs577792181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86385896 | AAACATAAAGCAGTA[C/T]TGAACAACACAGCCA | 11059 |
rs577830854 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468161 | CTTTTAATATGCACT[G/T]TAAATTTCATTAACT | 11059 |
rs577882344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344314 | TCTACATCAGGGTTT[C/T]GAAAAGCAATAATTA | 11059 |
rs577885286 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453235 | CTACCCTTCTACTTT[A/G]TTTCTGTGAGTTTGA | 11059 |
rs577901394 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419263 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGC | 11059 |
rs577919141 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363531 | TATGGGCCGAGCATG[G/T]TGGCTCACTCCTGTA | 11059 |
rs577925558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WWP1 | GRCh38.p7 | 8:86448762 | ATAGTGCTCACCACA[A/G]CCTGTTTCTTGAAAC | 11059 |
rs577949796 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450899 | GTTCTTCATAGGACA[-/T]TTATGTATTAGACTA | 11059 |
rs577976654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WWP1 | GRCh38.p7 | 8:86449330 | CATTTTCAGGAAAGA[A/G]CCAGGCAGTAAACTT | 11059 |
rs577978787 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WWP1 | GRCh38.p7 | 8:86413477 | ATGCCATGACAAGGA[A/G]TACATGCAGAGAAGG | 11059 |
rs577992696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86399772 | GAGAAATTCAAATGG[G/T]TTCTTTTACCTAGAC | 11059 |
rs578006007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86413980 | CAAAACAGTAAGTAC[A/G]TAAACCTAATTCTGT | 11059 |
rs578046214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86442384 | GGCATACAAATAAGC[A/T]TGTTATATCTATATG | 11059 |
rs578061371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86392686 | CTCTTTAGCCTTATT[A/G]ACTGAGTGAATTTGC | 11059 |
rs578062233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WWP1 | GRCh38.p7 | 8:86442997 | AGCCACTTAGTCTTT[A/G]AAAGTCCTTTCATTT | 11059 |
rs578063102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86406786 | TACCCTCTTTAAAGC[C/T]ACATCCACTCTCAAG | 11059 |
rs578077579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86393090 | ACTTCATCATTTATG[A/T]TTGTCTCATGCTCTT | 11059 |
rs578128576 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424721 | GAGGCGGGAGAATCA[A/G]GCAGGGAGGTTGCAG | 11059 |
rs578129604 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344031 | ACCAAATCTGTGTGT[A/C]TTATACAAGCAAAAT | 11059 |
rs578230578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86435161 | GATTTAAGGATTATC[A/G]AAGATTTTCTTTGAA | 11059 |
rs578239809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86427901 | CTATCCCTTGACCAT[A/T]ATCACATATCTATTT | 11059 |
rs578262688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WWP1 | GRCh38.p7 | 8:86421683 | CAAAAAATTAGCTGG[A/G]CGTGGTGGCTGGCGC | 11059 |
rs745311448 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378275 | TGTATTAAATTGGAG[C/G]TAATTGAAATATTTC | 11059 |
rs745311948 | snp | G/T | 1.65146e-05 | 0.0028735 | intron-variant | WWP1 | GRCh38.p7 | 8:86431757 | GTGTGAGTGAAAACC[G/T]GAAGTTCTCCTTTAA | 11059 |
rs745335087 | snp | A/G | 3.35289e-05 | 0.0040943 | intron-variant | WWP1 | GRCh38.p7 | 8:86430654 | TACTTTCATATTAAA[A/G]CACTGTTATTTTATT | 11059 |
rs745384961 | in-del | -/ACAC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362072 | TACACACATATATAT[-/ACAC]ATATATACACACATA | 11059 |
rs745404941 | in-del | -/T | 3.46837e-05 | 0.00416421 | intron-variant | WWP1 | GRCh38.p7 | 8:86380910 | TCACAAGAAAGTGTA[-/T]TTTTTTGGAATATGT | 11059 |
rs745438299 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437324 | GTTATACTAGCCTGT[A/G]AATAAATTCATCATT | 11059 |
rs745468899 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407361 | GATGGGCACATAGGT[-/A]ATCAGAGTTTCTCAA | 11059 |
rs745509421 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366364 | CATGGGCCAGGGAAG[A/G]ACAGTAGCACTAGTT | 11059 |
rs745514956 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419349 | CTTGAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 11059 |
rs745529117 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379741 | TTTCGAAGCTAACTT[G/T]CCAGATAAAACATTA | 11059 |
rs745534115 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458480 | TATGTATTTTTTTAG[C/T]GTGTGTGTTTTGCTT | 11059 |
rs745534692 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388786 | TCTTATTTTATTTGC[C/T]TAAGATTTTAAAAGT | 11059 |
rs745538674 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421482 | CTCTTAATAAAAAAA[A/T]AAATTTAATTGGGTT | 11059 |
rs745539340 | snp | A/C | 0.00033227 | 0.0128851 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398359 | GAAAGAGTGAAAGAA[A/C]AATTAAAACTTTCCT | 11059 |
rs745568104 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404938 | CTGCTAGGCTTCACA[C/T]AGCATTCCCCTAGCC | 11059 |
rs745629221 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371310 | AATTTTTTTGTTATT[A/G]TGAAGAATGCTTATA | 11059 |
rs745712311 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350932 | TTTGTATAAAGTAGG[A/C]TATTCTTTACCTTAG | 11059 |
rs745723521 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462460 | GGGAGATGAAAAAAT[C/T]GGGGGATGTAGGCAG | 11059 |
rs745724394 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428207 | GTCTTGCAGTATGCT[A/G]CCTATTCTGATTCTC | 11059 |
rs745725963 | snp | A/C | 1.75029e-05 | 0.00295823 | intron-variant | WWP1 | GRCh38.p7 | 8:86380695 | TACTTTTTGGCAACA[A/C]ATACTCACTAGTGAA | 11059 |
rs745796720 | snp | A/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411652 | GTACTACTGTTGAAG[A/T]TCCTCCAGTTCAAGA | 11059 |
rs745805116 | snp | C/T | 0.000188164 | 0.00969777 | downstream-variant-500B, intron-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468757 | TTCATCAGGGTCTTC[C/T]ACTTTTCATACCCAA | 11059 |
rs745815534 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436586 | TGTTCTGCCTAGTAC[A/G]TAGAATAGTGCCTTT | 11059 |
rs745816824 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395229 | GCCACCATAAGCAGA[A/G]GTTGTCCATAAAGAG | 11059 |
rs745821560 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402349 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 11059 |
rs745827094 | snp | C/T | 1.6549e-05 | 0.0028765 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411568 | CCTCATTTGCACCAA[C/T]TGATAATGCGTCTGT | 11059 |
rs745833820 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451239 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 11059 |
rs745853034 | in-del | -/TC | 4.95995e-05 | 0.00497969 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466851 | ACTAAAGGAAAAACT[-/TC]TTTTTGCAATAGAAG | 11059 |
rs745853949 | snp | A/C | 3.30136e-05 | 0.00406273 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435468 | ACTAAAGGTGGTCCA[A/C]AAATTGCTTATGAAC | 11059 |
rs745855455 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359749 | AATAATACTCTCTTT[C/T]ATCATTAAAAACAGT | 11059 |
rs745867548 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343579 | ATTTAATTTTGTAGT[C/T]TGCTCCTTACCTTTA | 11059 |
rs745907344 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361495 | GAAAATGTAGTGGTT[C/T]TGTATGGCTTTCCTG | 11059 |
rs745937186 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362998 | GCTTAATAATTTAGC[A/G]TTTATATAGTACTCG | 11059 |
rs745949941 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465110 | TGGGAGAATTGTTAG[A/C]GAATAGGCAAGTATT | 11059 |
rs745975087 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466112 | CCGAATCCTAATCTA[A/G]CTACTCAGTGCTGTA | 11059 |
rs745986760 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452430 | TACATATACACACAC[A/G]TCACATTTATATGTT | 11059 |
rs746007625 | snp | A/T | 1.65408e-05 | 0.00287578 | intron-variant | WWP1 | GRCh38.p7 | 8:86398669 | TGAATATGGGTGGCG[A/T]CATGATGTGGAACAT | 11059 |
rs746062554 | snp | A/T | 6.69142e-05 | 0.00578383 | intron-variant | WWP1 | GRCh38.p7 | 8:86430664 | TTAAAACACTGTTAT[A/T]TTATTTCTCTCCCTA | 11059 |
rs746093238 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439949 | ACCAAGTACAACTGA[C/T]GGGGATAGATAAGTA | 11059 |
rs746100431 | snp | C/T | 1.69252e-05 | 0.00290901 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448267 | TGAATTTTATAACTC[C/T]CTTATCTGGATAAGG | 11059 |
rs746102182 | snp | A/C/G | 3.33224e-05 | 0.0040817 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380863 | GATGAACAGCTAACT[A/C/G]TGTAAGTACCTTGTG | 11059 |
rs746118561 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400333 | GCAAGACTTCGTCTC[G/T]GGGGGAAAAAAATAA | 11059 |
rs746162328 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406972 | TGCTTTGAGATGGAT[A/G]TACCATAAAGTTCAT | 11059 |
rs746179892 | snp | C/T | 1.70009e-05 | 0.0029155 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438618 | TATGACTTGAGGAGG[C/T]GCTTATATGTAATAT | 11059 |
rs746203287 | in-del | -/TCTGTCTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457425 | CTGTCTGTCTGTCTG[-/TCTGTCTA]TCTGTCTATCTATCT | 11059 |
rs746284366 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444227 | AGATTAGATGCAGGG[G/T]TGTGAGAGAGAGTCA | 11059 |
rs746313081 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439342 | AGCAAGACGCTGTGT[-/C]AAAAAAAAAAAAAAA | 11059 |
rs746323332 | snp | C/T | | | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466657 | TAAATTTAGATTACT[C/T]TAAATACTTCTGGCA | 11059 |
rs746337366 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430299 | AGATATATTTTTGAG[A/T]CAGCTTCTCGCTCTG | 11059 |
rs746355667 | snp | A/G | 3.35441e-05 | 0.00409523 | intron-variant | WWP1 | GRCh38.p7 | 8:86435744 | AACACCATTTGTCTC[A/G]TTGTATTCTGTGCAT | 11059 |
rs746374616 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461807 | AGTTTTGCATTGAAA[A/G]AGTTGGCAAAGACAC | 11059 |
rs746379941 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402088 | AGTCCAAAACTCATG[C/T]TGCTCGTATGTAGTT | 11059 |
rs746384228 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444031 | GCTTGCTTTACGAGT[A/C]TGTAGAAGACAGACT | 11059 |
rs746386183 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409666 | GGAGTTCAAGACTGG[C/T]CTGGCCAACAAGGTG | 11059 |
rs746391786 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432422 | CTCTGCTGGTACATT[C/T]GATTCCTACCCCCAC | 11059 |
rs746396959 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346667 | ATAGCATGTTATTAC[A/C]TGTTAATAAACTTTG | 11059 |
rs746425861 | snp | A/G/T | 4.96219e-05 | 0.00498085 | intron-variant | WWP1 | GRCh38.p7 | 8:86461361 | TCTGTACGTAATTTT[A/G/T]TGATAATAATGGCCT | 11059 |
rs746433603 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341994 | ATAACCAACAGTACT[C/T]TTCTAAACTAGTTGA | 11059 |
rs746433660 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393826 | TAGTCCCCTCCCACA[C/G]TGCGTCAGAGATTAT | 11059 |
rs746455521 | snp | A/G | 0.000181937 | 0.009536 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435689 | GCAGACATTGTTTGA[A/G]GATTCCTTCCAACAG | 11059 |
rs746475245 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412022 | TTTATTTACTTGCTA[C/T]AAAACAAGTACTTTT | 11059 |
rs746478113 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358182 | ACTTTTGTATTGGAC[A/G]TTTTTCTATTGAGCA | 11059 |
rs746480061 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341311 | ACAGGAGAGATAGAG[A/C]ATGTGAGCATCAAAG | 11059 |
rs746533109 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342283 | ATTTATGGACAGCCT[A/G]CTTTTGCCCCCGGAC | 11059 |
rs746626718 | in-del | -/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363941 | TTTCCTTGAAAGGGT[-/TA]GGTTAGTTAGTTTTG | 11059 |
rs746657886 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435506 | TAGGTGGAAGCTTGC[C/T]CACTTCCGTTATTTG | 11059 |
rs746660985 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant | WWP1 | GRCh38.p7 | 8:86398644 | CAACTGCCAGGTAGA[A/G]TATTTTATTTGAATA | 11059 |
rs746673106 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434489 | TTTTTGCTCAAATGT[C/T]ACTTTGTCTGTGAGC | 11059 |
rs746697577 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378104 | AAAAAAATATTTTGA[A/G]AAATTTCCTTTTATT | 11059 |
rs746700404 | snp | A/T | 3.30961e-05 | 0.0040678 | intron-variant | WWP1 | GRCh38.p7 | 8:86461205 | ATTTCATATTAAAGT[A/T]CATTTAATTTCATTA | 11059 |
rs746757605 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383973 | GATTTTCTCACATAT[C/G]CAGAGGCTGGAAGTC | 11059 |
rs746792128 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349010 | GGGCTCACAAGAGTA[C/T]AAAACAGAAGCAACC | 11059 |
rs746929475 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408770 | AAAAATTTAGCCGGG[A/T]GTGGTGACGCATGCC | 11059 |
rs746929549 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426739 | AAATTGGCAGCAATA[C/T]AATGGCAGGAAGGTG | 11059 |
rs746941749 | snp | A/G | 1.68553e-05 | 0.00290299 | intron-variant | WWP1 | GRCh38.p7 | 8:86380887 | CCTTGTGTAAAGGAC[A/G]GAAAATCTTCACAAG | 11059 |
rs746954800 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410915 | CAGTAGGTTTTGTTC[G/T]GTAATCTATTCACCC | 11059 |
rs746958202 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369761 | TGCCTAGAGGAAGAA[A/G]TGTCTTTTTCTTGGA | 11059 |
rs746966342 | snp | A/G | 1.689e-05 | 0.00290598 | intron-variant | WWP1 | GRCh38.p7 | 8:86448307 | TTTGTTTTGCAATAA[A/G]TCATTTTTTTGAAAC | 11059 |
rs746967181 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371186 | ACAGGCATGAGCCAC[C/T]GCCCCTACCTGTAGT | 11059 |
rs746971224 | in-del | -/CATATATATA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430798 | AGATATATATCTCTC[-/CATATATATA]TATATATATATATAT | 11059 |
rs746974194 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351728 | TGATGGTTTTGCTGT[A/G]CAGCCTGGGAACAAG | 11059 |
rs746978277 | snp | A/C/G | 3.31352e-05 | 0.00407022 | synonymous-codon, missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411768 | GACACCTCTAATTCT[A/C/G]GAAGTAGTTCTGCTT | 11059 |
rs747023542 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450352 | GTGTGCATTTATTAC[A/G]CTAGTTGGAAAAAAA | 11059 |
rs747027118 | in-del | -/TGTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380716 | CACTAGTGAATTATT[-/TGTC]TGTTAGTTTCTAGTG | 11059 |
rs747029570 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391113 | AGACTCTCCTAACAT[A/C]AATTATTTGTATTGT | 11059 |
rs747046366 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461832 | AGACACTTGGTTACC[A/G]AGAAGCCATACATGG | 11059 |
rs747050311 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373254 | TTTCATTATATTTCA[A/G]TGTATTTTTTTTGTT | 11059 |
rs747077765 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346749 | TGATACAATTATAAT[A/G]AGCATTGGAAAATCC | 11059 |
rs747144019 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463740 | AACGAATGTTACAAA[A/G]TGACGCATGGGTAAA | 11059 |
rs747153297 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396539 | GGGGTATTCTATAAG[G/T]TCTTCTTTTATCACA | 11059 |
rs747190218 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374761 | CTCTCCCTGGCTGGA[A/G]TACGGTGGCGCAAAC | 11059 |
rs747200829 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432213 | CAGATTTAAAGATAC[C/T]TTAATTAAGCGGTTG | 11059 |
rs747214594 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396716 | CTCTCATCTCAGCCT[C/T]CTGAATAGCTGGGAA | 11059 |
rs747229026 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360540 | GGGTACCTGTCACAG[C/T]ATGGCTGGCTTTCAG | 11059 |
rs747263035 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399234 | CATACCGCTCTCTGG[A/G]TTGGCATTATCCTGT | 11059 |
rs747277527 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419285 | TAGCCAGGCATGGTG[A/G]CACGCGCCTGTAGTC | 11059 |
rs747325199 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366133 | GAGAGACTGTAGTTC[C/T]TGAGTTAAGCAGACC | 11059 |
rs747338983 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350759 | GCTGTTCAGTATACT[C/T]ATAAATCTGATTGAC | 11059 |
rs747372824 | in-del | -/GGG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389270 | TAAACATGTGAACAA[-/GGG]TCTGTGGTTTTCCTA | 11059 |
rs747382537 | snp | G/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367117 | TTTATTGAACTAAAC[G/T]GCTCTGTTACATATC | 11059 |
rs747437698 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425249 | GAAAAGATCCTCATG[A/G]TAGAACCTATTATGT | 11059 |
rs747487009 | snp | A/T | 1.86104e-05 | 0.00305038 | intron-variant | WWP1 | GRCh38.p7 | 8:86411905 | TAATGTCTGACTTGC[A/T]TTTAAGTAGCAACTC | 11059 |
rs747491029 | snp | A/G | 1.65282e-05 | 0.00287469 | intron-variant | WWP1 | GRCh38.p7 | 8:86442578 | TGTTTTTAAATTCAC[A/G]TATTAATGCTAAAAA | 11059 |
rs747496330 | snp | G/T | 1.65321e-05 | 0.00287502 | missense, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466858 | GAAAAACTTCTTTTT[G/T]CAATAGAAGAGACAG | 11059 |
rs747506268 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404826 | AATTGACATTCCGCT[A/G]TCTGGCTGTTGATTC | 11059 |
rs747521566 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443513 | ATTTACGTATTTATT[C/T]ACACTTTATTATCTA | 11059 |
rs747544213 | snp | A/C/G | 5.08861e-05 | 0.0050439 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438629 | GAGGCGCTTATATGT[A/C/G]ATATTTAGAGGAGAA | 11059 |
rs747572158 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355048 | CAAATAGAGTTGAAG[C/T]TTGCATGTAGGTCTG | 11059 |
rs747594373 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460062 | TAATCTGCTCCCTAT[G/T]TTCCTTGCTTTCTGT | 11059 |
rs747601081 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408654 | TGTGCAGTGGCTTAC[G/T]CCTGTAATCCCAGCA | 11059 |
rs747647939 | snp | A/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354985 | TTAATTTGGTGTTAT[A/G/T]ATCCTCATTTGACAG | 11059 |
rs747697204 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355938 | ATTAGCTTTGAGCCC[A/G]AGGAAATCTGGCTTC | 11059 |
rs747711963 | snp | C/T | 3.39092e-05 | 0.00411746 | intron-variant | WWP1 | GRCh38.p7 | 8:86380897 | AGGACGGAAAATCTT[C/T]ACAAGAAAGTGTATT | 11059 |
rs747712119 | snp | A/G | 3.42659e-05 | 0.00413906 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411857 | TGGGAATGCCAACAC[A/G]GAAACCTTGCCATCA | 11059 |
rs747713032 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379322 | AATTGCTATGTTGCC[A/G]GTACTTAAATATAGT | 11059 |
rs747722890 | snp | C/G | 1.71457e-05 | 0.0029279 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438602 | TATGGCATTAAAACC[C/G]TATGACTTGAGGAGG | 11059 |
rs747738044 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461339 | AATGTAATTTCACTG[C/T]AATTTCTCTGTACGT | 11059 |
rs747795104 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410406 | ATTTCAAACTCATTG[A/G]TATGAAATTGTACGT | 11059 |
rs747799334 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437168 | TGAGCTGTGCTCCAA[C/G]CCAGACTTGCCAGTC | 11059 |
rs747878965 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376223 | GGACAGTACACCTGA[C/G]GTGTAACTTTCAAAT | 11059 |
rs747889105 | snp | A/G | 4.95209e-05 | 0.00497574 | intron-variant | WWP1 | GRCh38.p7 | 8:86431517 | CAGCAGCCTTAAGTC[A/G]TCTTGCATATATCAG | 11059 |
rs747893275 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341240 | AGAAAATCTTAGTAC[A/C]TGTTTAAAGCAGAGA | 11059 |
rs747908301 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427738 | CCATGGAATCTGTCC[A/G]AAATTTTGAACAGTG | 11059 |
rs747969019 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348116 | TTAGGGAATGTATAA[C/T]GTAAAACCATACGTC | 11059 |
rs748009574 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439590 | TTCTTATTTTTTGCT[A/G]TTGTAAGTAACATCA | 11059 |
rs748037355 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438920 | TGCTGCTTTTTTTAA[C/T]AGTTAATCATACAAT | 11059 |
rs748037492 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453652 | CATTTTACATTCCTA[C/T]TAAACATGTAGAAAG | 11059 |
rs748066905 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422442 | TTGGCTCACTGCAAC[C/T]TCTACCTCCTGGGTT | 11059 |
rs748079223 | in-del | -/ATTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405326 | TCTGAAACCAAAAGG[-/ATTT]TTTTTTTTTTTTTTT | 11059 |
rs748088844 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425456 | TTATATAAATAATGA[A/G]TGTTCAGTCAATGAG | 11059 |
rs748093596 | snp | A/C | 3.63445e-05 | 0.00426274 | intron-variant | WWP1 | GRCh38.p7 | 8:86431365 | ATTTTATATATAGAT[A/C]CTAAATAGTTATTAA | 11059 |
rs748105819 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404597 | CATAAATAATTCTCA[A/T]GACATTCATAGTAAC | 11059 |
rs748121310 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345966 | GATTGTTGACAATGA[-/T]GGTGTTCTTTCATGT | 11059 |
rs748196962 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350604 | CACAAAGAAGGGCAC[A/G]GATAGAGTTACATGA | 11059 |
rs748201762 | in-del | -/CATATATATATA/TCT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430797 | AGATATATATCTCTC[-/CATATATATATA/TCT]CATATATATATATAT | 11059 |
rs748204466 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385682 | TCTGAGGTAACATTT[A/G]TAACAATTATAGACC | 11059 |
rs748231412 | in-del | -/GGGAGAGGGGGA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390708 | AGACGAGAGGGAGAC[-/GGGAGAGGGGGA]GGGAGAGGGGGAGGG | 11059 |
rs748293707 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428241 | CCAGATTCTAAGAAG[C/T]AACACTCATCTGTTT | 11059 |
rs748299213 | in-del | -/A | 0.0334418 | 0.12491 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468434 | CAAGCCTAAAGAATT[-/A]AAAAAAAAATTCTAA | 11059 |
rs748308484 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442376 | AAAAGTGTGGCATAC[A/G]AATAAGCATGTTATA | 11059 |
rs748323373 | snp | C/T | 1.6609e-05 | 0.0028817 | intron-variant | WWP1 | GRCh38.p7 | 8:86374016 | CATGAATAAATTCCC[C/T]TTTTTTAAAATAGGT | 11059 |
rs748348760 | snp | C/G | 0.000460267 | 0.0151632 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402187 | ACCACTCGCATCTGA[C/G]CCTGCCGATGACACT | 11059 |
rs748376275 | snp | C/T | 5.06633e-05 | 0.0050328 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411542 | TCCCTTCTCAGTTAA[C/T]GGAGAATCATCCTCA | 11059 |
rs748377856 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371428 | AATTATTTTCCAACA[C/G]GATTTTGCCATCTGA | 11059 |
rs748416440 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376991 | ACACTGAGAATCAGA[C/G]GGATTAAGTGCCTTG | 11059 |
rs748440731 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434809 | TGAACCTGACAACAC[A/C]AGAGAACATTTTTCA | 11059 |
rs748443475 | in-del | -/CAC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457554 | TAATAGATACACACA[-/CAC]ATTTAGATATAAATC | 11059 |
rs748467357 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364226 | GAATTTTATGTGTTG[C/G]TTGCTTTGAGGGAGA | 11059 |
rs748501459 | in-del | -/CTC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366506 | CTTCCCTCTTCCCTT[-/CTC]CTGACATGTAGTTCC | 11059 |
rs748508218 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467740 | AAATTGATGCAATTT[C/T]ATACTTAGGAACATA | 11059 |
rs748523786 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462520 | AATTAAAGAACTGAG[A/G]TGTCAAAGAAAAATT | 11059 |
rs748565197 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436079 | AACACCGGCATCTTA[C/T]ATTTCTCATTTTATT | 11059 |
rs748578485 | snp | C/T | 1.65105e-05 | 0.00287315 | intron-variant | WWP1 | GRCh38.p7 | 8:86398494 | AGTAAGCTAACTTTA[C/T]ATGTTTGTAAAATTT | 11059 |
rs748622179 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417988 | TGTCCGATAGTGACA[A/G]GTTCTATGAGACAAG | 11059 |
rs748644018 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389552 | GTCTCTTATGTCTAC[C/T]TCTTTCTACACAGAC | 11059 |
rs748679774 | snp | A/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452591 | GTTTTTCTCGAGGAG[A/T]ACAAGAACAGACCAA | 11059 |
rs748682525 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441677 | CTATGGTGTCCACCA[C/T]TGCCCAGTTGTCTGA | 11059 |
rs748709808 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402771 | GATTCTTAAGCTTTG[C/T]CACAAAAAATACTAT | 11059 |
rs748709823 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425282 | ATCATAATACTCGAA[C/T]TACCACATGGGAGAG | 11059 |
rs748727070 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456129 | CTTACCTCTGCCCAT[A/G]TAATTATTCATGCTT | 11059 |
rs748748958 | snp | A/G | 3.31923e-05 | 0.0040737 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381587 | TTATTAGGAAAAGCA[A/G]CGATAGATTTGAAAC | 11059 |
rs748750363 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365871 | TATACATTGAGAACA[A/C]CAAGTTTATTTGAAG | 11059 |
rs748819110 | snp | A/T | 1.70799e-05 | 0.00292227 | intron-variant | WWP1 | GRCh38.p7 | 8:86398325 | AAGCTTTTAAATTAG[A/T]ATATTCTTCTTTCTA | 11059 |
rs748823326 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405551 | TTGTTTGTTTTTTTG[-/A]GACAGGGTCTTGCCC | 11059 |
rs748836148 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368605 | AAACTTTAAAGTACT[A/G]TGCATGGTATATTTT | 11059 |
rs748874278 | snp | A/G | 1.66313e-05 | 0.00288364 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425229 | TTATTAAAGGTGGGA[A/G]CAAAGAAAAGATCCT | 11059 |
rs748896247 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459756 | TAGCTTCATTACAGT[C/T]GGTGTTCCATGGCTT | 11059 |
rs748915723 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422327 | CCAGTTTGTATTTAT[G/T]TATTTATTTATTTAT | 11059 |
rs748941357 | in-del | -/AA | 2.02649e-05 | 0.00318308 | intron-variant | WWP1 | GRCh38.p7 | 8:86381663 | CCTTTATTTCCTTAT[-/AA]GTTTATTTTAGACAC | 11059 |
rs748952586 | snp | A/C/G | 3.30171e-05 | 0.00406296 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381526 | TACGCCACAGACTAC[A/C/G]TTGGAATTTCAAGTT | 11059 |
rs748963057 | in-del | -/AT | 0.000373742 | 0.013665 | intron-variant | WWP1 | GRCh38.p7 | 8:86430784 | TGATCTATAAGGGAG[-/AT]ATATATATCTCTCCA | 11059 |
rs748970635 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408530 | TCAAGGAGAGTTGTT[A/T]ATTGTTTATTATTAT | 11059 |
rs749003889 | snp | G/T | 1.80699e-05 | 0.00300577 | intron-variant | WWP1 | GRCh38.p7 | 8:86411889 | GGTATGTTAAGCTTT[G/T]TAATGTCTGACTTGC | 11059 |
rs749024812 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395394 | AAAATAGGTAATGGA[A/C]CAGATTTTTGAGGAG | 11059 |
rs749039371 | snp | C/T | 0.000199114 | 0.00997584 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466927 | GAGGAGCTCTTGCAT[C/T]TAAATACCCCAGCCA | 11059 |
rs749116931 | in-del | -/TGA | | | downstream-variant-500B, cds-indel, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468468 | ATGTGACAGGTTATG[-/TGA]TAGAGGGAAACTGGC | 11059 |
rs749155862 | snp | C/T | 1.66529e-05 | 0.00288551 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411556 | ATGGAGAATCATCCT[C/T]ATTTGCACCAACTGA | 11059 |
rs749190769 | snp | C/T | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438670 | ATTATGGTGGCCTAG[C/T]GAGGTAAAATAAAAA | 11059 |
rs749193805 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437712 | ATTACTAATACCTAC[C/G]ATTGACTGGAAGCCT | 11059 |
rs749204210 | snp | G/T | 1.67666e-05 | 0.00289534 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402202 | GCCTGCCGATGACAC[G/T]GGTAAGCAAGGCTAT | 11059 |
rs749208541 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431743 | ATGGGAAGTCATCTG[C/T]GTGAGTGAAAACCTG | 11059 |
rs749217959 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396451 | CCTTTAGTTTTTCTA[A/G]TTGTTTGTTTTTTGT | 11059 |
rs749232032 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361847 | TGTCAATGAACTTAA[-/T]AATTGAGTCACGTGT | 11059 |
rs749238272 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396624 | TTTCAGACAGGGTCT[C/T]GCTCTATTACTCCCA | 11059 |
rs749259215 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | WWP1 | GRCh38.p7 | 8:86431528 | AGTCGTCTTGCATAT[A/G]TCAGTAGGTAGAACC | 11059 |
rs749265283 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380035 | AGAAATGAAAACATA[C/G]GTCCACAAAAAAGCC | 11059 |
rs749303129 | in-del | -/TCT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457426 | CTGTCTGTCTGTCTG[-/TCT]GTCTATCTATCTATC | 11059 |
rs749306163 | snp | C/T | 1.69496e-05 | 0.0029111 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448249 | TTTGGAATCTATTGA[C/T]ACTGAATTTTATAAC | 11059 |
rs749327525 | snp | G/T | 1.64735e-05 | 0.00286993 | stop-gained, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427728 | CAGCGGCCTACCATG[G/T]AATCTGTCCGAAATT | 11059 |
rs749330474 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364029 | GAGCACATTAAATTG[C/T]TCTGATCATATTTTC | 11059 |
rs749352767 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348380 | TGCACCACCACACCT[G/T]GCTAATTTTGTATTT | 11059 |
rs749365748 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455256 | TTTGAAAGTTTCCCA[C/T]TGAGTTTGGGAAAAA | 11059 |
rs749375342 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453994 | CATATGAAAAACAGC[A/T]CTTCAGATTTCATAC | 11059 |
rs749376324 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391800 | TAGCTGGCAAGTAAC[A/G]AAGTCAGGATTCTGT | 11059 |
rs749399663 | in-del | -/AAC | 1.65123e-05 | 0.0028733 | cds-indel, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442689 | GAGTATGCGGGCAAG[-/AAC]AACTATTGTCTGCAG | 11059 |
rs749434700 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366668 | AAGTTTCTTTGAGAT[A/T]CATCAAGAGAGCTGT | 11059 |
rs749476446 | snp | A/C/G | 3.52021e-05 | 0.00419524 | intron-variant | WWP1 | GRCh38.p7 | 8:86380675 | GATTGATTAGTGTGC[A/C/G]GTACTACTTTTTGGC | 11059 |
rs749481853 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405329 | GAAACCAAAAGGATT[-/TT]TTTTTTTTTTTTTTT | 11059 |
rs749529794 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411636 | TCTCCAAATTGCACT[A/G]GTACTACTGTTGAAG | 11059 |
rs749532840 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442227 | GTCATGTGCATAAAA[A/G]TGAATTAATATTGTG | 11059 |
rs749537755 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421023 | GTTAAGCTTTCATAC[A/C]GAATAGCCCATTGTT | 11059 |
rs749546428 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353351 | GATCTTTTTTCCTGG[A/G]AAAACCTAAAAATAT | 11059 |
rs749558008 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392183 | GAGGAAATCATTTGT[A/G]CTGAGTTTGCAGTTT | 11059 |
rs749562411 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385547 | GGATAAAAGTCCTTG[A/C]AGGCAGATTACAATA | 11059 |
rs749586257 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405940 | GGGGTTTAAGACAAA[C/G]GATATATTTCTGTCA | 11059 |
rs749686620 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432906 | AGCCATCACACCCAG[C/T]CCACAGTTCATTTTT | 11059 |
rs749722406 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446679 | AGTTTCATTCTTCTG[C/T]ATGAAGAAGCCAGCT | 11059 |
rs749730699 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462734 | TTTTCATACTAAGCC[A/G]TTATTTGCCTTTTTA | 11059 |
rs749737674 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415574 | CACGAGTCTTGAATG[C/T]ACCATTATGATGAAT | 11059 |
rs749745446 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466196 | TTTAAGCATTTTTTA[C/G]TATTTTAAAATTTTT | 11059 |
rs749756197 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376029 | TGAACTATAAGGGAT[A/C]TTTGGATTTTGGTTT | 11059 |
rs749846104 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363213 | ACGAGGAAACAACAA[C/T]AAAAAAAGCTGACTG | 11059 |
rs749867096 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414332 | AACACACTTCTTACT[G/T]TGTAAACTGTGGTCA | 11059 |
rs749918911 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460353 | AGTGGTTTAGGGCTC[A/G]TCTAGACTTGAGTTC | 11059 |
rs749921725 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361229 | TTATGGGCTTGGAGA[G/T]AAGAGTTGTAGTGGT | 11059 |
rs749924661 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362318 | AAAGATTAAATTAGA[A/G]GCTTATGTCAGTATT | 11059 |
rs749925332 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375435 | TGCCCTGTAGGTTCA[C/T]ATTTTTATTAGTTTT | 11059 |
rs750015761 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398615 | ACATGAAAATGGAGA[A/G]CCTTCAGCAAGGACA | 11059 |
rs750076594 | snp | C/T | 1.64947e-05 | 0.00287177 | stop-gained, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427803 | CAACAGTTTAACCAA[C/T]GATACCTCTATTCGG | 11059 |
rs750078692 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438519 | TAGAGATTAAATTTA[A/G]ATTGTTTTGAAAGGA | 11059 |
rs750107029 | snp | C/T | 3.30164e-05 | 0.00406289 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427665 | AGAAGAGTTGATGAT[C/T]GTAGAAGAGTTTATT | 11059 |
rs750114811 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399901 | CCAAATATATAGGCA[A/G]CAAGGGAAAGGAGGG | 11059 |
rs750129527 | snp | A/G | 1.69876e-05 | 0.00291436 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448201 | TTTACCATTCTACAA[A/G]CGTATGTTAAGTAAA | 11059 |
rs750135751 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439235 | GTAGTTCCAGCTACT[C/T]GGGAGGGTAAGGCAG | 11059 |
rs750180855 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343946 | CCTGAAATAGTTGGT[A/T]TACAGTTACCTGCAT | 11059 |
rs750198696 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351587 | CCCTACCTCGACCTC[C/G]CATAGTGCTGGGATT | 11059 |
rs750242304 | in-del | -/TGTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385211 | GCTCTATATAGAAAA[-/TGTT]TGATAGTCAGCACCT | 11059 |
rs750250094 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372782 | ATTTTTTTCCCCTTC[A/G]TTAGTCTTATCAGAC | 11059 |
rs750255116 | snp | C/G | 1.65337e-05 | 0.00287517 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411750 | AGAAGTATATTAGAG[C/G]CTGACACCTCTAATT | 11059 |
rs750287631 | snp | A/C | 1.93996e-05 | 0.00311439 | intron-variant | WWP1 | GRCh38.p7 | 8:86438559 | GCATGTGAGTATTTA[A/C]TATTCATGTTTTTGT | 11059 |
rs750308649 | snp | A/C | 1.65072e-05 | 0.00287286 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435658 | TACCTAGTCATGTAA[A/C]GATCAATGTGTCCCG | 11059 |
rs750328934 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436548 | TGTGAGCTCCATGAG[A/T]GCAGGGACTATTGGT | 11059 |
rs750333342 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429069 | ACCCGGGTTCTTTCT[C/G]CCCTTTTGCTCTGCC | 11059 |
rs750334175 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462233 | AACAGAGAACAACTA[A/G]CGGGAACCTACTTTG | 11059 |
rs750341818 | snp | C/T | 3.29924e-05 | 0.00406142 | intron-variant | WWP1 | GRCh38.p7 | 8:86461756 | CCAGATAAACTTTGT[C/T]TTATTTTCTTGGTGT | 11059 |
rs750384599 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413345 | TGTGGCAAAGACATA[C/T]AAGAAGCTGTTCTTA | 11059 |
rs750387459 | snp | A/C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464398 | TTTTCCCATTAAAAT[A/C/G]TTATGTTTATTTTCA | 11059 |
rs750395095 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461314 | GGAGGATTTGCTGAG[C/T]TCATGGGTAAATGTA | 11059 |
rs750397448 | snp | A/G | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402030 | CAAGGTTGGCTGTTG[A/G]AGGCACGAATGGAAT | 11059 |
rs750444457 | snp | A/G/T | 1.65045e-05 | 0.00287263 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374101 | TAACCACAGTGGAAG[A/G/T]TTGCAGTTACAGGTA | 11059 |
rs750455530 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429977 | GCTGAGGCGGGTGGA[A/T]CGCTTGAGCCTAGGA | 11059 |
rs750490522 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404036 | ATTTCTAATACAGGT[-/G]GAGTGTCTCTAATCT | 11059 |
rs750504832 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376575 | CTCTGTCTCAAAAAA[A/G]AAAGAAAGAAAAAGA | 11059 |
rs750514952 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394282 | GACTCAAATTGTTCT[G/T]TCTCAAATTGCTGTA | 11059 |
rs750526874 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434120 | CCTCTCTCTGCTTTC[C/T]TCCCACACCTTGTAC | 11059 |
rs750564858 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341524 | TGTTCAGTCAAGAGA[C/T]ACTTGTTGAATTCTG | 11059 |
rs750571078 | snp | C/T | 0.000149416 | 0.00864209 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381588 | TATTAGGAAAAGCAA[C/T]GATAGATTTGAAACA | 11059 |
rs750576816 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448018 | AATATTTTAGTTTTC[A/G]TGATTTATGCCATTC | 11059 |
rs750607666 | in-del | -/ATC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455192 | AGTTTGATAAAGGGA[-/ATC]ATCATCATCAACAAC | 11059 |
rs750611365 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466973 | ATAGTGTATATAAGC[G/T]GTTCATTCTGTACAG | 11059 |
rs750622621 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468515 | GCGTATACCATAAAA[G/T]AGTTAAGTATTAGAA | 11059 |
rs750624295 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | WWP1 | GRCh38.p7 | 8:86381466 | AATAGAATGACAACG[C/T]CTACTCCTGTATTTT | 11059 |
rs750628033 | snp | A/G | 1.65203e-05 | 0.002874 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448440 | GAGATTTTGGGAAAA[A/G]TTACTTCACATGACC | 11059 |
rs750652442 | in-del | -/ATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397499 | TGAAATGTACAACAC[-/ATT]ATTTACTATGTACAT | 11059 |
rs750674032 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427163 | GCGAAACGCCATCTC[-/A]AAAAAAAAAAAAAAG | 11059 |
rs750696091 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417592 | GTAAGTGCTTACTGA[A/T]TATTTGTTAGATGGT | 11059 |
rs750743664 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422265 | GGAAAATATTTTCTG[G/T]TTATTGTATTTTAAA | 11059 |
rs750745907 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348294 | CGCAATCTTGGCTCA[C/T]TGCAGCTTCCGCCTC | 11059 |
rs750788189 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457546 | GTATACATAATAGAT[-/A]ACACACACACATTTA | 11059 |
rs750813544 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369495 | AGAAAAATAGATTGG[A/G]GGTGGGGATCAGGGT | 11059 |
rs750829025 | snp | A/T | 1.80572e-05 | 0.00300471 | intron-variant | WWP1 | GRCh38.p7 | 8:86411494 | AGGTAATTGATTGCT[A/T]TATCATTACTTGATA | 11059 |
rs750835355 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448874 | AGAGTTTCACTCTGT[C/T]GCTCAGGCCGTCGTA | 11059 |
rs750875112 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459024 | TCTTTTTCTTTTTTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTGAGAC | 11059 |
rs750880501 | snp | A/G | 0.00028085 | 0.0118468 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402160 | CAGACCCAAAAATAC[A/G]CCAGCTCCAAAACCA | 11059 |
rs750900528 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360744 | ATCTTACCTTGCAGA[A/G]TTGGGGGTATGGATA | 11059 |
rs750927733 | in-del | -/TAAA | 3.60354e-05 | 0.00424457 | intron-variant | WWP1 | GRCh38.p7 | 8:86431367 | TTTATATATAGATCC[-/TAAA]TAGTTATTAAATATT | 11059 |
rs750931446 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462044 | AATATTTGAGAAATG[A/C]ATCCAGTGATTCAAC | 11059 |
rs750932311 | in-del | -/TTA | 1.70081e-05 | 0.00291612 | intron-variant | WWP1 | GRCh38.p7 | 8:86427620 | TTGAGAGATTATTGT[-/TTA]TTATTGTTTACTTGT | 11059 |
rs750936669 | snp | G/T | 1.66103e-05 | 0.00288182 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431432 | GATTCAACAGACAGG[G/T]TTTACTTTGTGAATC | 11059 |
rs750948404 | snp | G/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452662 | TGGCTACAGTACTTC[G/T]ATGAAAAAGAATTAG | 11059 |
rs750985260 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372511 | TTCCATCCTGAGAGG[A/T]CACAAAACAATAGTT | 11059 |
rs751012742 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428923 | AATGAGGTAACAGAT[G/T]TGTATCAGAAGAATG | 11059 |
rs751041916 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355636 | GAATACGTGGAAATT[A/T]TGTGTTAAACATGAT | 11059 |
rs751163738 | snp | C/G | 3.30011e-05 | 0.00406195 | intron-variant | WWP1 | GRCh38.p7 | 8:86461338 | AAATGTAATTTCACT[C/G]TAATTTCTCTGTACG | 11059 |
rs751170217 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413130 | CATGCCTGGCCAGCT[C/T]TCCATCATTTTAACT | 11059 |
rs751182631 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463247 | TGGTGGTGATAATTA[C/G]CACCATGAGCTTGAC | 11059 |
rs751184350 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462368 | GAAATGCTGAAGTAA[A/G]CAAAGACCCCGAAGA | 11059 |
rs751203429 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402046 | AGGCACGAATGGAAT[A/G]GATAATCATGTACCT | 11059 |
rs751234023 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449862 | AGTACAGTTAAATCT[A/G]ACTCATTTTTTAATA | 11059 |
rs751274016 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414147 | ACATAATGAAATAAA[G/T]AAATATAGGCGAGAA | 11059 |
rs751275557 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344523 | AATTTCTGCCTTCAC[A/G]CTAATTAGGTAGATA | 11059 |
rs751281687 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360976 | ATTCAGGGTAATTAG[A/G]TTGAGGAATGTCAGG | 11059 |
rs751284414 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365349 | TGGAGGGAAGATAGT[C/T]GAAGTTATTAGATTC | 11059 |
rs751302879 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378514 | AAAATACTTATATAA[C/T]CTTAGAGTGGAGGAC | 11059 |
rs751327320 | in-del | -/T | 8.78279e-05 | 0.00662618 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466743 | AAGTATTCTATTAGA[-/T]TTTTTTTCATTTTAT | 11059 |
rs751334096 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401943 | CTTAAGAGAATTTAG[C/T]AAATCCTATGAAAAT | 11059 |
rs751337671 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350211 | TATCTGGGTTTTTCT[C/T]GCATTATCACTTAAC | 11059 |
rs751376295 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | WWP1 | GRCh38.p7 | 8:86381474 | GACAACGTCTACTCC[C/T]GTATTTTTGTTAATA | 11059 |
rs751382475 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385485 | AGTATGATTTCTGGC[-/A]AGACATTTTTTTAAA | 11059 |
rs751387364 | snp | A/G | 3.30071e-05 | 0.00406232 | intron-variant | WWP1 | GRCh38.p7 | 8:86411903 | TTTAATGTCTGACTT[A/G]CATTTAAGTAGCAAC | 11059 |
rs751419374 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346017 | TTACCATCAATTAAA[C/T]ATAGTTACTGCCTTT | 11059 |
rs751446949 | in-del | -/AAAAAAAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439343 | CAAGACGCTGTGTCA[-/AAAAAAAAA]AAAAAAAAAAAAAAG | 11059 |
rs751475642 | snp | A/G | 5.03233e-05 | 0.00501589 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411832 | GTATGGATCCTGTAC[A/G]GCAGCAGTCTGGGAA | 11059 |
rs751475667 | snp | A/G | 0.000719166 | 0.018949 | intron-variant | WWP1 | GRCh38.p7 | 8:86440584 | GTCCTTTTTCCTGAA[A/G]TTCAATAATTTCACT | 11059 |
rs751477414 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442124 | AAACCTGTTGTATAT[A/C]CATCCTAGAGTGCTT | 11059 |
rs751524730 | snp | G/T | 1.7648e-05 | 0.00297047 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438587 | TGTTTTTAATTAGAT[G/T]ATGGCATTAAAACCC | 11059 |
rs751530711 | snp | A/G | 4.96718e-05 | 0.00498331 | intron-variant | WWP1 | GRCh38.p7 | 8:86427828 | ATTCGGTAATTAGCA[A/G]ATTGTAAGATGTTAA | 11059 |
rs751558280 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354361 | CTGTAGTTTGTTTGG[C/G]AAATGCTTGTGTGTG | 11059 |
rs751571385 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463112 | TCTTTTATGGAACAC[-/T]TATTTTTACTTGAAA | 11059 |
rs751574383 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408069 | TTATCCCTCAAACCC[G/T]TTGCAACAGCTGTTT | 11059 |
rs751579168 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401505 | GTTGAAGCTGCAGTG[A/T]GCCACTGCACTCCAG | 11059 |
rs751631392 | in-del | -/AAAAAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360069 | CAAAAAACAAAAAAC[-/AAAAAAA]AAACACAATCCTCTA | 11059 |
rs751644854 | snp | C/T | 8.23974e-05 | 0.00641809 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431664 | GAAATTAGATATACT[C/T]GTGAAGGTGTAAGGT | 11059 |
rs751657299 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369139 | GTTGTCATAAAAAAT[A/G]TGGCTATAGACTTCT | 11059 |
rs751679155 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355449 | GCCAAAATATTAAAA[A/C]TTTTTGAATTTTAAG | 11059 |
rs751701567 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403447 | ATTACAGGTGTGTGC[C/T]ACCATGCCCCCTAAT | 11059 |
rs751719760 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460691 | TAGTGGCCAGCCTCC[A/G]TGTTCTCATGAGGAT | 11059 |
rs751734054 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340981 | GTCAATAACAAAAGG[C/G]TGGTTCAATATTGGG | 11059 |
rs751744022 | in-del | -/GGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404734 | TAACTCCTTGAAATA[-/GGT]GGTAGTATTTTTCCT | 11059 |
rs751785002 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434058 | CCCCCATTGCCACCA[-/T]TTTGGTCCAAGCTAC | 11059 |
rs751818013 | snp | C/T | 1.93414e-05 | 0.00310972 | intron-variant | WWP1 | GRCh38.p7 | 8:86381649 | GTTTTTTGTTCTGAC[C/T]TTTATTTCCTTATAA | 11059 |
rs751849768 | snp | A/G | 3.39968e-05 | 0.00412277 | intron-variant | WWP1 | GRCh38.p7 | 8:86452545 | CTATTTTTAAATACC[A/G]TCTTTATTTTCAGTT | 11059 |
rs751851760 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433814 | TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGGAGA | 11059 |
rs751903148 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346211 | AGTTAGCAATATCAG[A/C]TCATTCATTTGGATT | 11059 |
rs751914338 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352745 | CTTCCAGATGTTTAA[A/G]ACAGCCTAAGATAAT | 11059 |
rs751919157 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422229 | AACACTGCCTTCTCG[A/G]GTTCTTGTGTTTAAG | 11059 |
rs751926066 | in-del | -/AT | 5.08023e-05 | 0.0050397 | intron-variant | WWP1 | GRCh38.p7 | 8:86425364 | TATATTTTATCACAC[-/AT]GTGGTTTTTAAATTT | 11059 |
rs751958525 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | WWP1 | GRCh38.p7 | 8:86374152 | TTTAATATGGTGATT[C/T]CCTGATGAACTTTTC | 11059 |
rs751972767 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391152 | GAATCCAACTAACTG[C/T]GTCTTGTTAGGGAGA | 11059 |
rs752000662 | in-del | -/AGTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393174 | TTATTTTTTTCTCTC[-/AGTT]AGTTAATCATTAGCC | 11059 |
rs752012409 | snp | C/T | 1.79803e-05 | 0.0029983 | intron-variant | WWP1 | GRCh38.p7 | 8:86411505 | TGCTTTATCATTACT[C/T]GATAGATGATTTTAT | 11059 |
rs752012490 | snp | A/G | 1.66136e-05 | 0.00288211 | intron-variant | WWP1 | GRCh38.p7 | 8:86374006 | TTATCTAACACATGA[A/G]TAAATTCCCCTTTTT | 11059 |
rs752050769 | in-del | -/T | 1.66813e-05 | 0.00288797 | intron-variant | WWP1 | GRCh38.p7 | 8:86374168 | CCTGATGAACTTTTC[-/T]TTTGAATACCTAATT | 11059 |
rs752054790 | snp | G/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411589 | ATGCGTCTGTCACGG[G/T]TACTCCAGTAGTGTC | 11059 |
rs752078878 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420607 | AACAAATCACAATAA[G/T]TCAAGGAAGTTAATA | 11059 |
rs752079213 | snp | G/T | 0.000757002 | 0.0194404 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468412 | TTATGAACACTCTGG[G/T]AATTTTCAAGCCTAA | 11059 |
rs752090679 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441956 | CGCATATTGGACTTT[A/C]AAATGGGTGGTAAAA | 11059 |
rs752107594 | snp | A/G | 1.84415e-05 | 0.00303651 | intron-variant | WWP1 | GRCh38.p7 | 8:86435419 | ATTCAACTTTATTAT[A/G]AGTTAATTTGGTTTA | 11059 |
rs752120231 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449189 | ATTTCCTAAATGTAG[A/G]CATTTTTCCAAGATT | 11059 |
rs752132153 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376565 | TAAAGTGAGGCTCTG[C/T]CTCAAAAAAAAAAGA | 11059 |
rs752141518 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350406 | ATTTTAAGAATTTAG[C/G]TTATTAGTGCATAGC | 11059 |
rs752150227 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387039 | CATCCGTGAGGACTG[C/T]GCCCTCTTGATTTAA | 11059 |
rs752189706 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426363 | TGTATTTTTAGTAAT[A/T]AGTTTAAGGAATTTA | 11059 |
rs752197881 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385129 | CTAAAAACATTTTTT[A/G]TTCCTATCCTTAAAT | 11059 |
rs752204319 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370954 | CACTGCAACCTCTGC[C/T]TCCCGGGTTTAAGTA | 11059 |
rs752228291 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400332 | GCAAGACTTCGTCTC[-/G]GGGGGGAAAAAAATA | 11059 |
rs752245986 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462240 | AACAACTAACGGGAA[C/T]CTACTTTGGGTTGGG | 11059 |
rs752250712 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442123 | AAAACCTGTTGTATA[C/T]ACATCCTAGAGTGCT | 11059 |
rs752308058 | snp | C/T | 0.000330196 | 0.0128448 | intron-variant | WWP1 | GRCh38.p7 | 8:86440652 | GATCTTCCTTAATGT[C/T]AGGGAAGTTTTCTTC | 11059 |
rs752308874 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412248 | ACTGGAGAGCAAATA[G/T]CTCTTCTTTTCCTCA | 11059 |
rs752309357 | snp | C/T | 3.29826e-05 | 0.00406082 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402149 | CAGGTTGCTGCCAGA[C/T]CCAAAAATACACCAG | 11059 |
rs752313783 | snp | C/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461798 | GGCCTCAAAAGTTTT[C/G]CATTGAAAAAGTTGG | 11059 |
rs752317802 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360068 | CAAAAAACAAAAAAC[-/A]AAAAAAAAAACACAA | 11059 |
rs752328448 | in-del | -/AGCCGAC | | | utr-variant-5-prime, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342910 | CGCCCGGCTGCCGGG[-/AGCCGAC]AGCCGACAGCTTCGC | 11059 |
rs752350336 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357874 | TTTTCCTTGTAAAGT[A/G]TTAACAATTTGGCTG | 11059 |
rs752388655 | in-del | -/CTGTAATTTCT | 1.64996e-05 | 0.0028722 | intron-variant | WWP1 | GRCh38.p7 | 8:86461336 | GTAAATGTAATTTCA[-/CTGTAATTTCT]CTGTACGTAATTTTG | 11059 |
rs752393499 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376446 | TAGTGGCACATGCCT[A/G]TAATCCCAGCTACTT | 11059 |
rs752480786 | snp | A/T | 1.64988e-05 | 0.00287213 | intron-variant | WWP1 | GRCh38.p7 | 8:86452715 | TATTGTAGGGAATGT[A/T]AGTGGGGGGAGGGAC | 11059 |
rs752484751 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387957 | CTGTATCTCTGCTAT[C/T]CAATATGGTAGCCTT | 11059 |
rs752484822 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86435262 | TTCTTTGTGTATATG[A/T]GTGTCCTGTTGCTGT | 11059 |
rs752496220 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362629 | GAGCCCCAAATCTGT[C/T]TGATGACCAAAAAAG | 11059 |
rs752526696 | in-del | -/ATTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412478 | TAATATTAATTAATG[-/ATTA]ATTGTCTCTGCCTTC | 11059 |
rs752533227 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398421 | TGAATTGACAGTTGT[A/G]CTTGATGGATTGGTG | 11059 |
rs752555908 | snp | A/G | 8.28947e-05 | 0.00643743 | missense, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466820 | TGGATCTACCACCAT[A/G]TAAGAGTTATGAACA | 11059 |
rs752583475 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442721 | GATAAATCCAGCATC[A/G]ACCATTAATCCAGAC | 11059 |
rs752584705 | snp | C/G | 1.70769e-05 | 0.00292202 | intron-variant | WWP1 | GRCh38.p7 | 8:86425368 | TTTTATCACACATGT[C/G]GTTTTTAAATTTATT | 11059 |
rs752586364 | snp | C/T | 1.72931e-05 | 0.00294045 | intron-variant | WWP1 | GRCh38.p7 | 8:86398307 | CATTTTTATATGTGG[C/T]AAAAGCTTTTAAATT | 11059 |
rs752610939 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454664 | AGAGGTGCACTCAGA[A/G]AGGGATGTTATAGTG | 11059 |
rs752663967 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456189 | TGAAAGTGAAAAACA[C/T]AAGAGAAATCTTGAT | 11059 |
rs752715875 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415267 | GTTTCCCCACATTTC[C/T]GTATCCTGCTTTATT | 11059 |
rs752746410 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348635 | ACAGATATGAAGCCT[C/T]TCCTCTTGGAACCTG | 11059 |
rs752785038 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351901 | GAGTGGAGCTTAGGG[A/T]TCTTCATTTTTTGCA | 11059 |
rs752831418 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368000 | TCCATGGACCTGTTT[C/T]CTCAACTGCATGCTT | 11059 |
rs752846318 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361017 | GAGGAGAAGGAAGAG[-/GT]GGGGCAACAGATCAC | 11059 |
rs752895568 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457682 | GTTTTTCTTGAAGAA[C/T]ACTCTAAATGCGGTT | 11059 |
rs752898501 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407558 | ACTAAATGTCTTTGG[C/T]GGTGGGGAGAGCAGA | 11059 |
rs752944503 | snp | C/T | 1.77395e-05 | 0.00297816 | intron-variant | WWP1 | GRCh38.p7 | 8:86435428 | TATTATGAGTTAATT[C/T]GGTTTATTTTTGTTT | 11059 |
rs752945571 | in-del | -/T | 1.73966e-05 | 0.00294924 | intron-variant | WWP1 | GRCh38.p7 | 8:86411531 | TTTATTAATTTTCCC[-/T]TCTCAGTTAATGGAG | 11059 |
rs752983180 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353919 | GAATACCGAACAGAA[C/T]GTATATATTATACTT | 11059 |
rs752995914 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445044 | CACAAGGGGAAGCAG[C/T]GTGTATGAAAGTCAC | 11059 |
rs752999713 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457984 | AATACTGTTTATCGA[C/T]ATTATACAAGAAACA | 11059 |
rs753017132 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390916 | TCCCTATTGTTTTCT[C/T]GTATATTTCATGGTT | 11059 |
rs753061595 | snp | A/G | 1.65562e-05 | 0.00287712 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448401 | GAAGAATGTGGCTTA[A/G]AAATGTACTTTTCTG | 11059 |
rs753076124 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345779 | AGAACTCTTACTGTA[C/G]AGATATGCTGTATAT | 11059 |
rs753100311 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426408 | AAGGAGTTTACAATC[A/G]TTTTATAAATTAATG | 11059 |
rs753113497 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377849 | TTTTTAGCTATTGTG[A/T]CTTCTAAAGCATTTT | 11059 |
rs753125568 | snp | C/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344425 | GGTGGCTGAAATTTC[C/G]TTTACTTCCTTGTAC | 11059 |
rs753153847 | snp | C/T | 1.66952e-05 | 0.00288917 | intron-variant | WWP1 | GRCh38.p7 | 8:86374171 | GATGAACTTTTCTTT[C/T]GAATACCTAATTCAG | 11059 |
rs753162248 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449709 | ATGTCTTCTATGAAT[A/G]GTACTACCATTTTCA | 11059 |
rs753217875 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355857 | CTTCTCATTTTAAGG[C/T]ATGGGTTAGCTCAGC | 11059 |
rs753221585 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389649 | ATCATCATCATGGCC[C/T]GTTCTCAATGAGCTG | 11059 |
rs753224474 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438044 | TGACCTCGTGATCCA[C/G]CTGCCTTGGCCTTCC | 11059 |
rs753247176 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396155 | CCAGGCTGGAGTGCA[G/T]TGGCGCGATCTCAGC | 11059 |
rs753264630 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411725 | CAGTGCAGAATTGGA[A/G]TCTGAAGCTAGAAGT | 11059 |
rs753301969 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400033 | TTACATTCTGATGGG[A/G]TAAAGGTAGATAGTA | 11059 |
rs753344218 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349657 | GCTTACTACGCAAAT[A/G]GGAATACCTAGCACT | 11059 |
rs753352388 | in-del | -/AATG | 1.64817e-05 | 0.00287064 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461242 | GTGAAAGAGACAGAC[-/AATG]AAGTAAGAATGCGAC | 11059 |
rs753365556 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363524 | ATATGTCTATGGGCC[A/G]AGCATGGTGGCTCAC | 11059 |
rs753388742 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362088 | CACATATATACACAC[-/AT]ATATATATACACTAG | 11059 |
rs753435651 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412694 | CACTATGTTAGTGTA[C/T]GTTGGTTTTTTTTTT | 11059 |
rs753443447 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443234 | CACACCACCATGCCA[A/G]CTAATTTTTTTGTAT | 11059 |
rs753449472 | in-del | -/CTACCTTCTCT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394414 | ATGTTTTTTAAGCAC[-/CTACCTTCTCT]CAGTTGCTGAGGATA | 11059 |
rs753454818 | snp | C/T | 1.67323e-05 | 0.00289239 | intron-variant | WWP1 | GRCh38.p7 | 8:86427634 | TTTATTATTGTTTAC[C/T]TGTGGTAGTTGGGAA | 11059 |
rs753489450 | snp | C/T | 1.6534e-05 | 0.00287519 | splice-donor-variant | WWP1 | GRCh38.p7 | 8:86374122 | GTTACAGGTAACTGG[C/T]AAGTTATTTTTATAT | 11059 |
rs753495269 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369566 | CTGATTGGCACTGTT[C/G]CCCAGTTTGCACAGT | 11059 |
rs753515378 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86431788 | ATATTGCTTAGTGAG[C/T]ACATGAGATTTAGTC | 11059 |
rs753522685 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442757 | TTCATACTTCTGTTT[C/T]ATTGGTCGTTTTATT | 11059 |
rs753540316 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391861 | TATCCTTCCCAATGA[C/T]TGCATTTTAAAGGAA | 11059 |
rs753551691 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384563 | CAGCCTTGAAGCAAT[C/T]TAAAAATACTTTTAT | 11059 |
rs753575982 | snp | A/G | 0.000497059 | 0.015757 | intron-variant | WWP1 | GRCh38.p7 | 8:86440719 | TCCATTTTTCTTCAG[A/G]AACATCAGTCATGGG | 11059 |
rs753579687 | snp | A/G | 0.000188094 | 0.00969595 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468373 | GATCTGCTTGGTTGA[A/G]TAGACTCCTTTTCCA | 11059 |
rs753591524 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384832 | ATGGTGAAACCCCAT[C/T]TCTACCAGAGATACA | 11059 |
rs753618687 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364550 | TTTAAAAATAAAAAA[C/T]ATTTCAGTGCTTTGG | 11059 |
rs753636438 | snp | A/T | 4.99197e-05 | 0.00499573 | splice-acceptor-variant | WWP1 | GRCh38.p7 | 8:86435450 | TTTTTGTTTTTCTTT[A/T]GAACTAAAGGTGGTC | 11059 |
rs753658919 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462030 | TTCTCATTAATAGAA[A/C]TATTTGAGAAATGCA | 11059 |
rs753661841 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340769 | TGGCACTGGGTGGCA[A/G]AGCTGTGTTTTGATG | 11059 |
rs753678548 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398602 | ATGGTGATGCCTTAC[A/G]TGAAAATGGAGAGCC | 11059 |
rs753684215 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401965 | TATGAAAATTCTCAT[G/T]AAATGTTGTTGAATT | 11059 |
rs753712492 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436478 | CAGCCATTTATGGTG[C/T]TTTATTCTTTTTCAT | 11059 |
rs753729231 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465905 | TTATTTAGATGCCTT[C/G]TTTCAAAGGCTCTTT | 11059 |
rs753733811 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427765 | AGTGGCAATCTCAGC[A/G]GAACCAATTGCAGGG | 11059 |
rs753735898 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460157 | GTCAATGAAATAGAT[A/G]ATTTTAGAGGAATGT | 11059 |
rs753739107 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462338 | AGTACGCAGAGAAAG[A/G]GCATTCTTTGAACAG | 11059 |
rs753754612 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341203 | TATTTAAAGGGACCA[G/T]ACAGCAAAAGCAAAA | 11059 |
rs753813691 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453107 | TATTTTTAAGTGTTC[A/G]ATAATGTTAAATATA | 11059 |
rs753820908 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398396 | ACAAGAATGGCATAG[C/T]ACAAACTGGTGAATT | 11059 |
rs753854970 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454779 | GCAGGGTTTATAATG[G/T]TCTCACATACTGCCC | 11059 |
rs753855631 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436827 | CAGGCATACAGGGAC[C/T]TTTATTTATACTTTG | 11059 |
rs753860223 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415915 | TCAAAACTATGCCTA[C/T]CGTATAGCAGGCACT | 11059 |
rs753931665 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365510 | GTCTGGTAGATATTG[C/T]AAGTACTCTTCAAAT | 11059 |
rs753944391 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344323 | GGGTTTTGAAAAGCA[A/G]TAATTATGAGCTACC | 11059 |
rs753955889 | snp | A/G | 1.65715e-05 | 0.00287845 | intron-variant | WWP1 | GRCh38.p7 | 8:86381463 | ATTAATAGAATGACA[A/G]CGTCTACTCCTGTAT | 11059 |
rs753967378 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378800 | ATTTTGGATGGATCT[C/G]TAATGAACTCAGAGA | 11059 |
rs753988766 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359058 | AAATCTGTATGAGAA[A/T]CACCTAGAATGCCCA | 11059 |
rs754011648 | snp | A/G | 1.66866e-05 | 0.00288842 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411817 | GACAGCCAGATGGGT[A/G]TATGGATCCTGTACG | 11059 |
rs754013780 | snp | A/G | 1.65842e-05 | 0.00287955 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380819 | TTACGAAAACAGCAA[A/G]ATCCAGTAGTTCTTC | 11059 |
rs754016024 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427018 | AATACAAAAAATTAG[C/T]TGGGCATGGTGGTCT | 11059 |
rs754068799 | snp | A/G | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411739 | AATCTGAAGCTAGAA[A/G]TATATTAGAGCCTGA | 11059 |
rs754079621 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378309 | GTTAAACTTTTCAAA[A/T]CTAGGAATATATCAT | 11059 |
rs754100633 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452152 | TCACGGCAATGCTTG[G/T]TGTAAGAAGAGCCTG | 11059 |
rs754127848 | in-del | -/CT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423030 | ATAGACACTTTGTGC[-/CT]CTTGGATTTAATATT | 11059 |
rs754193543 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397986 | AATAAGTAGCAGAAC[A/T]GGAATTTGAAACCAA | 11059 |
rs754253704 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357697 | TTCTGGATAAAAGTA[G/T]CTATAATTTGTTTTG | 11059 |
rs754269556 | snp | A/C | 1.66485e-05 | 0.00288513 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431425 | AAGAGTGGATTCAAC[A/C]GACAGGGTTTACTTT | 11059 |
rs754292684 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462133 | AAGTTTGTGCCCCAT[A/G]GTGGGGCACAAATGA | 11059 |
rs754299143 | snp | A/G | 8.24002e-05 | 0.0064182 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402066 | ATCATGTACCTACAA[A/G]CACTCTAGTCCAAAA | 11059 |
rs754323020 | snp | C/T | 1.74385e-05 | 0.00295278 | intron-variant | WWP1 | GRCh38.p7 | 8:86448551 | GCTTAATTTCTAGAA[C/T]ACTTCAGAACTAAAT | 11059 |
rs754325086 | snp | A/T | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448227 | GTAAAAAACTTACTA[A/T]TAAGGATTTGGAATC | 11059 |
rs754375920 | snp | G/T | 1.65416e-05 | 0.00287586 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448413 | TTAGAAATGTACTTT[G/T]CTGTTGACATGGAGA | 11059 |
rs754381920 | snp | A/T | 4.94287e-05 | 0.00497111 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411623 | AGAAAATGCCTTGTC[A/T]CCAAATTGCACTAGT | 11059 |
rs754426880 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395444 | GGCTGCAGGTTTTTG[A/G]ACACTAATGAAAAAC | 11059 |
rs754435365 | snp | C/T | 1.75585e-05 | 0.00296293 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438589 | TTTTTAATTAGATTA[C/T]GGCATTAAAACCCTA | 11059 |
rs754486223 | snp | A/G | 1.66228e-05 | 0.0028829 | intron-variant | WWP1 | GRCh38.p7 | 8:86435710 | CTTCCAACAGGTAAG[A/G]AGGATTTTAGCAGAA | 11059 |
rs754544417 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451261 | AAAAAAAAGATACAT[A/G]AAAGCTTGCCCGATA | 11059 |
rs754554173 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383327 | GTTTTCAATTCTGTT[A/G]TGTTAGACTCTACTG | 11059 |
rs754555410 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405121 | AAAGGATGAATTCAG[A/G]TATCTTTTCAAGGAG | 11059 |
rs754561993 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440674 | GTTTTCTTCTATTAT[A/G]TCTTTGAATATTTTT | 11059 |
rs754583831 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422331 | TTTGTATTTATTTAT[G/T]TATTTATTTATTTAT | 11059 |
rs754625024 | in-del | -/CATT | 1.64823e-05 | 0.0028707 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431710 | ACACAAGAACAACAA[-/CATT]CAAAGATCCTCGCAA | 11059 |
rs754625801 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438761 | CATATGTGAATATAT[-/TG]TATTAAATTTTTGAA | 11059 |
rs754659044 | snp | G/T | 4.02325e-05 | 0.00448494 | intron-variant | WWP1 | GRCh38.p7 | 8:86381659 | CTGACCTTTATTTCC[G/T]TATAAGTTTATTTTA | 11059 |
rs754678034 | in-del | -/CCA | 0.00018655 | 0.00965609 | intron-variant | WWP1 | GRCh38.p7 | 8:86430797 | GAGATATATATCTCT[-/CCA]TATATATATATATAT | 11059 |
rs754690181 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410294 | AAAACCTTTCTGAGC[C/T]TGGAGCCTTTAGGAG | 11059 |
rs754692802 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355714 | CACTTATCTTTTTAC[A/G]ATTAATTGTTCTTTC | 11059 |
rs754705436 | in-del | -/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399502 | GAAAAAGCATGCTAG[-/TA]TATATGACAAAGTGT | 11059 |
rs754710411 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383635 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11059 |
rs754713572 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461154 | TATTTAATTTCTTCA[A/G]GTGTCTACTACTTTC | 11059 |
rs754723040 | snp | C/T | 3.29674e-05 | 0.00405988 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402055 | TGGAATAGATAATCA[C/T]GTACCTACAAGCACT | 11059 |
rs754788827 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86431815 | AGTCTCTAATTTATC[C/G]TCAAGTTTAGCAAAA | 11059 |
rs754794465 | snp | C/T | 1.67908e-05 | 0.00289743 | intron-variant | WWP1 | GRCh38.p7 | 8:86452552 | TAAATACCATCTTTA[C/T]TTTCAGTTTAATGAC | 11059 |
rs754797613 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455217 | AACAACAAAAAACCT[C/T]AGCATTATTCTAAAT | 11059 |
rs754801966 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465912 | GATGCCTTGTTTCAA[A/T]GGCTCTTTCCTGACT | 11059 |
rs754838137 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414517 | ACACAGCACCAGGCT[C/G]TGTAACCCTTTGAGT | 11059 |
rs754866591 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375504 | AGATACATGTGCAGT[A/G]TACGTATCTCATCTC | 11059 |
rs754893450 | snp | A/G | 8.46962e-05 | 0.00650699 | intron-variant | WWP1 | GRCh38.p7 | 8:86425210 | TACTGTTATTTTTGT[A/G]TTTTTATTAAAGGTG | 11059 |
rs754925349 | snp | C/T | 1.66394e-05 | 0.00288434 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381595 | AAAAGCAACGATAGA[C/T]TTGAAACAAGCTCTG | 11059 |
rs754944012 | snp | G/T | 1.68579e-05 | 0.00290321 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411839 | TCCTGTACGGCAGCA[G/T]TCTGGGAATGCCAAC | 11059 |
rs755033627 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436836 | AGGGACTTTTATTTA[C/T]ACTTTGTACAAGCCA | 11059 |
rs755045351 | snp | G/T | 1.78662e-05 | 0.00298878 | intron-variant | WWP1 | GRCh38.p7 | 8:86411513 | CATTACTTGATAGAT[G/T]ATTTTATTAATTTTC | 11059 |
rs755052603 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418960 | GTTCTCTAACAAAAC[A/G]GTCCCATTATTATCA | 11059 |
rs755081900 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468667 | TGCTGGTCTCCCTCA[A/C]GTAAGAAATTACGAT | 11059 |
rs755090529 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447093 | TGTGATTACCAGGAA[A/G]CAGACCAGTGATGAA | 11059 |
rs755099784 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442321 | AAAATTGTTGAAATG[A/G]GATTTAAGCTGAATT | 11059 |
rs755101744 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399642 | TTAAGTACATATATT[A/T]AATGTCCATATAATT | 11059 |
rs755103962 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404407 | GATATAAAAAGGAGA[C/T]GAAATTGAGGCTTTC | 11059 |
rs755136878 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456891 | CAAAAATATGTATGT[A/G]TGCATATATATGACA | 11059 |
rs755164630 | in-del | -/AC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353201 | AAATTAATGAAAGAA[-/AC]AAAACAAATTTCAAG | 11059 |
rs755182699 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350491 | TAATGCAAATCTCTT[C/T]GCAAATTTCTGAAAA | 11059 |
rs755182860 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366885 | AGAAGTAATATTACT[A/G]TATTCGTATATATAA | 11059 |
rs755218394 | snp | A/G | 1.65056e-05 | 0.00287272 | intron-variant | WWP1 | GRCh38.p7 | 8:86431514 | ATACAGCAGCCTTAA[A/G]TCGTCTTGCATATAT | 11059 |
rs755265807 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387714 | TTTTTGGTAGAGATG[A/G]GGTTTCACCATGTTA | 11059 |
rs755271191 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462137 | TTGTGCCCCATGGTG[C/G]GGCACAAATGACAAA | 11059 |
rs755299743 | snp | A/G | 1.67469e-05 | 0.00289364 | intron-variant | WWP1 | GRCh38.p7 | 8:86442805 | ACTTTATTATTATTT[A/G]TTTAAGTTTGTTACA | 11059 |
rs755309529 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446683 | TCATTCTTCTGTATG[A/C]AGAAGCCAGCTGGGG | 11059 |
rs755354517 | snp | C/T | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448394 | CAACATTGAAGAATG[C/T]GGCTTAGAAATGTAC | 11059 |
rs755357434 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393472 | AGGCTGATCTTGAAC[A/T]CCTCAAGTGATCCAC | 11059 |
rs755410214 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376826 | CTGTGCTAAATGGCA[C/T]CAGGTTTTAGTGCCT | 11059 |
rs755426707 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341771 | AGGAGCAGGGACATC[C/T]AGCCTCCGAGATAGA | 11059 |
rs755444915 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352938 | AAGCTAATTCTTTTT[-/A]AAAAAATGCCTACTA | 11059 |
rs755456055 | snp | C/T | 3.29614e-05 | 0.00405951 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411682 | AAATACTGACTTCCT[C/T]AGAAAACAATGAATG | 11059 |
rs755470484 | snp | A/G | 1.66192e-05 | 0.00288259 | intron-variant | WWP1 | GRCh38.p7 | 8:86374157 | TATGGTGATTCCCTG[A/G]TGAACTTTTCTTTTG | 11059 |
rs755478026 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420074 | CTTTCTTAGAAAGCT[A/G]CTAGGACTTGTGTTT | 11059 |
rs755483784 | snp | A/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411593 | GTCTGTCACGGGTAC[A/T]CCAGTAGTGTCTGAA | 11059 |
rs755525898 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | WWP1 | GRCh38.p7 | 8:86374012 | AACACATGAATAAAT[C/T]CCCCTTTTTTAAAAT | 11059 |
rs755533180 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377736 | TATTTTAGATTTTAG[A/G]CTTTCAACAGGAAAC | 11059 |
rs755550054 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451685 | TCTAGAAAGCAAAAA[A/G]AAGAGTTAGAAATGG | 11059 |
rs755594608 | snp | C/G | 0.000163653 | 0.00904431 | intron-variant | WWP1 | GRCh38.p7 | 8:86440691 | CTTTGAATATTTTTT[C/G]TGTTCCATTTGTTCC | 11059 |
rs755605029 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412313 | CTGATTGGCTCTATT[A/G]AAAATGCAGTTTTTC | 11059 |
rs755626522 | in-del | -/CCTC | 1.67002e-05 | 0.00288961 | intron-variant | WWP1 | GRCh38.p7 | 8:86427852 | ATGTTAACATAACTT[-/CCTC]CCTCAGGTGTTTCTT | 11059 |
rs755660986 | snp | C/T | 1.7243e-05 | 0.00293619 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411862 | ATGCCAACACAGAAA[C/T]CTTGCCATCAGGGTA | 11059 |
rs755675655 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452992 | GCTTCAAAGATCAGA[A/G]TTTTAAGTCATGAGT | 11059 |
rs755687317 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398115 | TATTTAAATGTATTT[A/G]TATGTTCTCCAAAAT | 11059 |
rs755711382 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438528 | AATTTAAATTGTTTT[C/G]AAAGGAACTTGTACT | 11059 |
rs755745625 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383120 | TAATTTTTATATATT[C/T]GGCTTAAAACTTTTT | 11059 |
rs755762311 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421552 | AAAATAGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 11059 |
rs755768796 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346372 | AGCTTGTAGTGAGCC[A/G]AGATTGCGCCACTAC | 11059 |
rs755787820 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347644 | ACCACAGAATAGTTA[C/T]TCTCCTGTCAAGGAT | 11059 |
rs755860486 | snp | C/T | 1.70589e-05 | 0.00292047 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438609 | TTAAAACCCTATGAC[C/T]TGAGGAGGCGCTTAT | 11059 |
rs755876815 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353527 | GACGGAGTCTCACTC[-/T]TGTTGCCCAGGCTGG | 11059 |
rs755897749 | snp | A/G | 3.32873e-05 | 0.00407953 | missense, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466802 | TGTTCAGTTTTAATC[A/G]CTTGGATCTACCACC | 11059 |
rs755922522 | snp | A/G | 0.000329772 | 0.0128366 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431732 | AGATCCTCGCAATGG[A/G]AAGTCATCTGTGTGA | 11059 |
rs755942418 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406461 | CACAAGTTTATTATA[-/T]TTTTTTCTTAGCTCT | 11059 |
rs755988712 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429094 | TCTGCCATCCATATC[A/G]CACTTCAGGCCTGTT | 11059 |
rs756036521 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361266 | GGTAAGAAGTAATTG[G/T]CCTAGGCAGAAATCT | 11059 |
rs756057526 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414415 | GAGGTAAATGCTAAT[A/G]TTTTAGGTTGACATA | 11059 |
rs756076852 | in-del | -/TTTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405327 | CTGAAACCAAAAGGA[-/TTTT]TTTTTTTTTTTTTTT | 11059 |
rs756098401 | snp | C/T | 1.71968e-05 | 0.00293225 | intron-variant | WWP1 | GRCh38.p7 | 8:86398317 | TGTGGCAAAAGCTTT[C/T]AAATTAGAATATTCT | 11059 |
rs756103018 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374206 | CTTATTCCAGAAATA[G/T]AATTTCTTTTAGATT | 11059 |
rs756125364 | in-del | -/TTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405328 | TGAAACCAAAAGGAT[-/TTT]TTTTTTTTTTTTTTT | 11059 |
rs756130115 | snp | G/T | 1.71158e-05 | 0.00292534 | intron-variant | WWP1 | GRCh38.p7 | 8:86427607 | TCATTTTCTTATATT[G/T]AGAGATTATTGTTTA | 11059 |
rs756151238 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467025 | AGTATGTTTTCCGTT[C/G]TTCCACAGAAATATG | 11059 |
rs756179012 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359629 | ATCTCAGAGTAAGAG[C/T]GGTTTTGTCTATACC | 11059 |
rs756179088 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388079 | TTTAAATAGCCATAC[A/G]TGGCCGCTGGCTACT | 11059 |
rs756215182 | snp | A/G | 0.000187846 | 0.00968958 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468651 | CAGTTCGTTTTCAGG[A/G]TGCTGGTCTCCCTCA | 11059 |
rs756215598 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341540 | ACTTGTTGAATTCTG[C/T]ACACACTCATGAAGT | 11059 |
rs756251352 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417630 | AAATACTTGAAGTTA[A/C]CTCAGGATAAAACAG | 11059 |
rs756260344 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404490 | TTCTTTCCATTGGTA[A/G]TAAGTTCAGTTCTCG | 11059 |
rs756328974 | snp | C/G | 1.68675e-05 | 0.00290405 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411543 | CCCTTCTCAGTTAAT[C/G]GAGAATCATCCTCAT | 11059 |
rs756334938 | in-del | -/AAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364833 | AGAAAGAAAGAAAGA[-/AAG]AGAGAGAGAGAGAGA | 11059 |
rs756347748 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454944 | GAGAAAATACAGATT[C/T]TGTCTTGTTTTGCTT | 11059 |
rs756364152 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365388 | GATAGGCATTTTTAG[A/G]CTTCAATACCTTTTA | 11059 |
rs756416537 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468521 | ACCATAAAAGAGTTA[A/C]GTATTAGAATTACAA | 11059 |
rs756442651 | snp | A/T | 1.73024e-05 | 0.00294124 | intron-variant | WWP1 | GRCh38.p7 | 8:86435434 | GAGTTAATTTGGTTT[A/T]TTTTTGTTTTTCTTT | 11059 |
rs756445406 | snp | C/T | 1.71823e-05 | 0.00293101 | intron-variant | WWP1 | GRCh38.p7 | 8:86427859 | CATAACTTCCTCCCT[C/T]AGGTGTTTCTTTCTT | 11059 |
rs756446307 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459708 | TACAGTATGCATACC[A/G]TTGTTTGTAATCTTC | 11059 |
rs756456685 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449836 | AGCTTACTTTTTTTT[G/T]TCTTAAGGACAGTAC | 11059 |
rs756459180 | snp | A/G | 1.6766e-05 | 0.00289529 | intron-variant | WWP1 | GRCh38.p7 | 8:86430768 | TAAGCTGTTTTTGCT[A/G]ATGATCTATAAGGGA | 11059 |
rs756477829 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395382 | CTTTATTTATGAAAA[A/T]TAGGTAATGGACCAG | 11059 |
rs756482816 | snp | A/G | 1.65518e-05 | 0.00287674 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448403 | AGAATGTGGCTTAGA[A/G]ATGTACTTTTCTGTT | 11059 |
rs756504098 | snp | A/G | 3.303e-05 | 0.00406373 | intron-variant | WWP1 | GRCh38.p7 | 8:86398646 | ACTGCCAGGTAGAAT[A/G]TTTTATTTGAATATG | 11059 |
rs756537722 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392120 | ATGGTGGTGCTTGCT[C/G]AAGTCTTTTAGTGTG | 11059 |
rs756547277 | in-del | -/CT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427422 | AAGAAAATAAGCAAA[-/CT]CTTGTAGTGCAGGAC | 11059 |
rs756634471 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86424590 | GGCAGATCACTCGCC[A/G]TTAGGAGCTGGAGAC | 11059 |
rs756643368 | in-del | -/G | 1.65116e-05 | 0.00287324 | intron-variant | WWP1 | GRCh38.p7 | 8:86431570 | AATGAGATATTTTTA[-/G]TACCTAGAAAAGGTT | 11059 |
rs756645608 | snp | A/G | 1.69893e-05 | 0.00291451 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448212 | ACAAGCGTATGTTAA[A/G]TAAAAAACTTACTAT | 11059 |
rs756657544 | snp | C/T | 3.29799e-05 | 0.00406065 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398453 | TTGAGCAAGAAAATA[C/T]AACAAACTGCAGCTC | 11059 |
rs756750338 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428937 | TGTGTATCAGAAGAA[C/T]GTTATCTTGCAAGTA | 11059 |
rs756759998 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395147 | TAGGACGTATCATCA[A/C]ACCACTGGTAAAAAT | 11059 |
rs756832515 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413171 | TATGTTCAGGCCAGA[C/G]TTTTCTTTGAGCTTA | 11059 |
rs756859272 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464122 | AGATTTTGTATAACA[A/C]AGTACAAAGTGTTCT | 11059 |
rs756859494 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449895 | TAGGTACATTGTGGT[A/G]TATTTTTTTCTATAT | 11059 |
rs756865918 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397727 | TGAGTTTAAATAAGA[A/G]CTAGATGTTCTAATA | 11059 |
rs756887477 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396246 | TGGGACTACAGGCAA[C/T]TGCCACCATGCCCAG | 11059 |
rs756893324 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344577 | TGTCTTTTAATATAT[A/G]AGTTTCATAAATGGT | 11059 |
rs756896047 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348241 | TTTTTTTTTTGAGAC[A/G]GAGTTTCCCTCTTGC | 11059 |
rs756912816 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451476 | ATAATGAGTGTGGTG[A/G]TAAAGGGAGGACAGA | 11059 |
rs756966363 | snp | A/G | 3.30186e-05 | 0.00406303 | intron-variant | WWP1 | GRCh38.p7 | 8:86435616 | AGATGATATTATGAT[A/G]TTATTTTTGTTTTTA | 11059 |
rs756975354 | snp | C/G | 1.66261e-05 | 0.00288319 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425230 | TATTAAAGGTGGGAA[C/G]AAAGAAAAGATCCTC | 11059 |
rs756982094 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379715 | TATTTGAAAATGCAA[A/G]TACTACTTCTTTTCG | 11059 |
rs756999920 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384550 | ATAAGGTTCAAGACA[A/G]CCTTGAAGCAATTTA | 11059 |
rs757014900 | snp | A/G | 1.65105e-05 | 0.00287315 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442778 | TCGTTTTATTGCCAT[A/G]GTGAGTTCCTGACTT | 11059 |
rs757022377 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350362 | TTTTATTACATTATA[G/T]CTTCTGAGTGGAGTA | 11059 |
rs757023371 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436546 | AATGTGAGCTCCATG[A/G]GAGCAGGGACTATTG | 11059 |
rs757044822 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456736 | ATAAGCAAATTGTTG[C/T]ATATTCATATAATGG | 11059 |
rs757051807 | in-del | -/TATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464241 | ATCTCCATTTCTAAC[-/TATT]TATCTGTGTGGGGCT | 11059 |
rs757064879 | snp | A/T | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402104 | TGCTCGTATGTAGTT[A/T]ATGGAGACAACACAC | 11059 |
rs757068816 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442138 | TACATCCTAGAGTGC[C/T]TGTAAGAGTTAAGAA | 11059 |
rs757081841 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411641 | AAATTGCACTAGTAC[C/T]ACTGTTGAAGATCCT | 11059 |
rs757090241 | snp | A/G | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435453 | TTGTTTTTCTTTAGA[A/G]CTAAAGGTGGTCCAC | 11059 |
rs757120136 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428069 | AGTTTTATATCCTAC[A/G]GGGTAGTTTCATAAA | 11059 |
rs757133332 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385413 | AAAGAAGAGAACAGC[A/G]AAAGACAATCTAGCT | 11059 |
rs757162550 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372661 | TATGGATAATTCCAG[A/G]TTTCTTTAAGTGTCC | 11059 |
rs757172016 | in-del | -/TTTG | 0.000187837 | 0.00968933 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466773 | TTGAAAACATCTGAT[-/TTTG]TTTTTGTTTCTGTTC | 11059 |
rs757186456 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371207 | TACCTGTAGTTCATT[C/T]GTTCTCACTACTATA | 11059 |
rs757218844 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362218 | CTGGAAAACTTCATT[A/C]AAAAAATTGTTAAAA | 11059 |
rs757229104 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387582 | CAGGGGTGCAGTCTC[A/G]GCTCACTGCAGCCTT | 11059 |
rs757241754 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398603 | TGGTGATGCCTTACA[C/T]GAAAATGGAGAGCCT | 11059 |
rs757256027 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434350 | TTCACCGTGTTCTAG[C/T]TTCATTGGACGCTAG | 11059 |
rs757288642 | snp | A/G | 3.36627e-05 | 0.00410246 | intron-variant | WWP1 | GRCh38.p7 | 8:86458057 | TTTTTGAAACAAAGT[A/G]CTCAACATATTTTCT | 11059 |
rs757299775 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342553 | GGGAGGCGGATTCCG[A/G]GTCCGGAGTTGGAGG | 11059 |
rs757334475 | snp | A/G/T | 3.38623e-05 | 0.00411463 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448260 | TTGATACTGAATTTT[A/G/T]TAACTCCCTTATCTG | 11059 |
rs757352321 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445327 | TAGGTAGTTTTTCAA[C/T]CCTTGCCTTCCTCCC | 11059 |
rs757352807 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388160 | GAATTTATCTCTGCC[-/T]TTTTTTTTTTTTTAA | 11059 |
rs757377992 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378360 | GTTTCCATTGGTAAA[A/G]TTTTATAGTTCTCTT | 11059 |
rs757383304 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391979 | CTAAGAAAGAGTAGT[C/T]GGGGGCCTATCATCA | 11059 |
rs757388570 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375688 | TTTGCTGGACATTGG[C/T]GTTCCACTGTTTGCT | 11059 |
rs757420987 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341036 | ACTAAGAGCTTCTGA[A/C]CGGGGAGGAAATTGA | 11059 |
rs757430853 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427020 | TACAAAAAATTAGCT[A/G]GGCATGGTGGTCTGC | 11059 |
rs757439265 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362940 | TAACTTTCATTATTG[A/G]AAATTGTTTCTCGTA | 11059 |
rs757459439 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432239 | GGTTGACAGATCTCT[C/T]CTTCATTCTTACTCT | 11059 |
rs757512337 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415234 | GTGTTTTTTGAGTCT[C/T]CTGTCCAAATCAAGC | 11059 |
rs757550098 | snp | A/C | 1.65842e-05 | 0.00287955 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380823 | GAAAACAGCAAAATC[A/C]AGTAGTTCTTCTAAT | 11059 |
rs757560533 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438379 | CGGGTCAACTATATG[C/T]GAAAGTGAGTCAGGA | 11059 |
rs757595282 | snp | A/T | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457951 | ATGCAGGAGGTTGAC[A/T]TGGCAGATTGGCAGA | 11059 |
rs757603124 | snp | A/G | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411743 | TGAAGCTAGAAGTAT[A/G]TTAGAGCCTGACACC | 11059 |
rs757662348 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372447 | TTACAGGAGTGAATA[G/T]TCACACTTTTCTTAT | 11059 |
rs757674502 | snp | A/C | 1.64893e-05 | 0.0028713 | stop-gained, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461799 | GCCTCAAAAGTTTTG[A/C]ATTGAAAAAGTTGGC | 11059 |
rs757693639 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402078 | CAAGCACTCTAGTCC[A/G]AAACTCATGCTGCTC | 11059 |
rs757711077 | in-del | -/ATTATTGTTT | 0.000119579 | 0.00773146 | intron-variant | WWP1 | GRCh38.p7 | 8:86427612 | TTCTTATATTGAGAG[-/ATTATTGTTT]ATTATTGTTTACTTG | 11059 |
rs757747889 | snp | C/G | 1.66443e-05 | 0.00288477 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431426 | AGAGTGGATTCAACA[C/G]ACAGGGTTTACTTTG | 11059 |
rs757763810 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391125 | CATAAATTATTTGTA[C/T]TGTTTTCCCCAGAAT | 11059 |
rs757777503 | in-del | -/AGA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425773 | TATACCTAAAATTGT[-/AGA]AGGTTTTAAATTAAT | 11059 |
rs757778230 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408092 | AGCTGTTTTTAAATA[C/T]TGGCTCTATAGTTTT | 11059 |
rs757804824 | snp | A/G | 5.27162e-05 | 0.00513374 | intron-variant | WWP1 | GRCh38.p7 | 8:86430781 | CTAATGATCTATAAG[A/G]GAGATATATATCTCT | 11059 |
rs757810582 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354494 | AGGATTGTGTCCCTG[A/T]ATTTTGGATTCTAAT | 11059 |
rs757811861 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365077 | AAGATGTAAAAATTA[A/G]AGAGTAAGAGAAAAC | 11059 |
rs757815541 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368318 | AACTGGAAATGAAAT[C/T]CAAATAATCTTACTC | 11059 |
rs757827524 | in-del | -/AAAAG | 1.68136e-05 | 0.0028994 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380743 | TCTAGTGCCAAACTT[-/AAAAG]AAAAAAGAACTGGTT | 11059 |
rs757830347 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426421 | TCATTTTATAAATTA[A/G]TGACAAAAATTGGTT | 11059 |
rs757883340 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410483 | TTGGAAAGGTATATT[G/T]CATGGTTTCTCCAGC | 11059 |
rs757890527 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442057 | AATAAAGTTAAAAGT[A/G]TTAAATAGCAGCAGT | 11059 |
rs757945391 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438404 | CAGGAAAAGCTTAAC[-/A]AGATTGATATGTATG | 11059 |
rs757963925 | snp | A/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427707 | AACACCAGAACAACA[A/G]CGTGGCAGCGGCCTA | 11059 |
rs757974670 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388854 | GCAGTCTTTTAAATC[A/C]GACCTGAGTTGCTTT | 11059 |
rs757976710 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419504 | AGAACCCAATGCTAT[A/G]AAAATGGAATACTCA | 11059 |
rs758007712 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368057 | GTTGTTAGCAATTTT[-/C]TTTTGAACTGCATAT | 11059 |
rs758067176 | snp | C/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463190 | TTTCTTGAGAAGTAA[C/G/T]GATGTTAGCTTGTCA | 11059 |
rs758098761 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342087 | CGGACACGTATACTC[A/G]GTCAATAAGTATCTG | 11059 |
rs758102490 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407402 | GTTGACATATTGGCC[C/G]AGGTAATTCTTTGTT | 11059 |
rs758108001 | snp | A/G | 3.29973e-05 | 0.00406172 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398628 | GAGCCTTCAGCAAGG[A/G]CAACTGCCAGGTAGA | 11059 |
rs758125015 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362433 | TAGGTGTAAGGTGGC[A/C]ACTGTTTGGCCTTGG | 11059 |
rs758142464 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394729 | TCTGACACACACATA[C/T]ACAAACACATGTAGA | 11059 |
rs758156424 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453589 | ATATGGTAATCCTCT[A/G]TTTAATTTTTTGAGG | 11059 |
rs758187270 | in-del | -/AAAAAAAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439341 | AGCAAGACGCTGTGT[-/AAAAAAAAA]CAAAAAAAAAAAAAA | 11059 |
rs758191851 | in-del | -/TTTTG | 4.99264e-05 | 0.00499607 | intron-variant | WWP1 | GRCh38.p7 | 8:86461893 | AAGCCACAGAGAATC[-/TTTTG]TTTTGTTTTTTTAAA | 11059 |
rs758197791 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348190 | TTATAAGGAAGAGTA[A/G]CATTTGTTGATTTAG | 11059 |
rs758199395 | snp | A/T | 9.06725e-05 | 0.00673261 | intron-variant | WWP1 | GRCh38.p7 | 8:86438579 | CATGTTTTTGTTTTT[A/T]ATTAGATTATGGCAT | 11059 |
rs758222919 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401803 | AGTAATTAAAACTTT[A/G]ATATAAAACATGTCA | 11059 |
rs758242371 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396566 | ACATGGTTTAAACAT[-/T]TTTTTTTTTTTTTTG | 11059 |
rs758248743 | in-del | -/ATG | 1.65176e-05 | 0.00287376 | intron-variant | WWP1 | GRCh38.p7 | 8:86435611 | AACTCAGATGATATT[-/ATG]ATATTATTTTTGTTT | 11059 |
rs758257052 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416378 | CAGGTTGATCTGCTG[A/G]TGCAGTAGGTCAGTG | 11059 |
rs758257928 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400252 | CAGGAGAATTGCTTG[A/C]ACCCGGGAGGCGGAG | 11059 |
rs758264838 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440868 | GCAGTACTGCCCTAC[A/G]TTTTGCTGCTTCTAA | 11059 |
rs758312228 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417502 | TAGTTTGAGAAAGAC[A/T]AATTCTATTTAGAAC | 11059 |
rs758319485 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367832 | CTGAGGGCTTGTGAT[A/T]AGCACAGTATTAATA | 11059 |
rs758344151 | snp | C/T | 1.65553e-05 | 0.00287705 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411759 | TTAGAGCCTGACACC[C/T]CTAATTCTAGAAGTA | 11059 |
rs758356277 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343956 | TTGGTTTACAGTTAC[C/T]TGCATTTTTTTTTTT | 11059 |
rs758374166 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409550 | TGATTTTACTTTATT[C/T]TTGATCTTAATAGAA | 11059 |
rs758375024 | snp | A/C | 3.30191e-05 | 0.00406306 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435662 | TAGTCATGTAAAGAT[A/C]AATGTGTCCCGGCAG | 11059 |
rs758418379 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404463 | CTACAGCTTGTCTGA[-/G]TACTTTATAGATTCT | 11059 |
rs758424117 | in-del | -/AGA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404800 | GCACAGCTAGGAAGT[-/AGA]AGAACTGTAATTGAC | 11059 |
rs758432108 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459425 | AAGGAAGATGCTAAC[C/G]AATGTGTATAATATG | 11059 |
rs758436565 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351949 | TATGCACATTAGTTT[C/G]AGAACTGTTGGTAGA | 11059 |
rs758442249 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351310 | GCTTCGTTTTGGCAT[-/G]GGCAGAGCTCCTTAT | 11059 |
rs758467063 | in-del | -/TATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86431161 | ATATTATAGAATATA[-/TATT]TATTATATTCTACAT | 11059 |
rs758487846 | snp | C/T | 3.26813e-05 | 0.00404223 | intron-variant | WWP1 | GRCh38.p7 | 8:86430788 | TCTATAAGGGAGATA[C/T]ATATCTCTCCATATA | 11059 |
rs758522430 | snp | A/T | 1.75919e-05 | 0.00296574 | intron-variant | WWP1 | GRCh38.p7 | 8:86452531 | CACATATAAATTACC[A/T]ATTTTTAAATACCAT | 11059 |
rs758534319 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353979 | TTGGTAATTGTAACT[G/T]GTTTTAAAACTTTCT | 11059 |
rs758537063 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406621 | ACATGAATACAACCC[A/C]TACAGCTTGTTCACA | 11059 |
rs758571178 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443450 | TTTAAGCGCTTTGCA[A/G]AAGCCCTTATGGAAC | 11059 |
rs758574272 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374632 | TGATATTTCCAATTC[A/G]TAATAATAACTGTAG | 11059 |
rs758596820 | snp | C/G | 1.65707e-05 | 0.00287838 | intron-variant | WWP1 | GRCh38.p7 | 8:86381467 | ATAGAATGACAACGT[C/G]TACTCCTGTATTTTT | 11059 |
rs758605834 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457376 | AATAGGTTTGGAACT[A/G]ATGAATTTGGATAGC | 11059 |
rs758619244 | snp | A/T | 0.000132127 | 0.00812686 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448442 | GATTTTGGGAAAAGT[A/T]ACTTCACATGACCTG | 11059 |
rs758722633 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368816 | GTTATCTTCTCTGTG[A/G]TCCCTTTCTTGATCC | 11059 |
rs758738071 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437128 | TAGCACTGAGCCCAC[A/G]ACTGCCTCCAAGGAG | 11059 |
rs758761975 | in-del | -/T | 1.65486e-05 | 0.00287646 | intron-variant | WWP1 | GRCh38.p7 | 8:86374128 | GTAACTGGTAAGTTA[-/T]TTTTTATATTTAATA | 11059 |
rs758787938 | snp | C/G | 0.000168336 | 0.00917277 | intron-variant | WWP1 | GRCh38.p7 | 8:86440733 | GGAACATCAGTCATG[C/G]GTATGTGGAATCTCC | 11059 |
rs758903097 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396189 | TTGCAACTTCCACCT[C/T]CCGAATTCAAGCAAT | 11059 |
rs758940344 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379277 | AAGACCCTGGTAGTA[A/G]CAGTTCAGACATAAC | 11059 |
rs758955066 | snp | A/C | 5.03428e-05 | 0.00501686 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402172 | TACACCAGCTCCAAA[A/C]CCACTCGCATCTGAG | 11059 |
rs759033286 | snp | C/G | 1.75511e-05 | 0.0029623 | intron-variant | WWP1 | GRCh38.p7 | 8:86402226 | AGGCTATTTATGACA[C/G]CTTGTTTAAAGGAAA | 11059 |
rs759034429 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374565 | CAGAGCTAGGAAATG[C/T]TTCTTGTAGAAAGCA | 11059 |
rs759037149 | snp | C/T | 1.75452e-05 | 0.00296181 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466744 | AAGTATTCTATTAGA[C/T]TTTTTTCATTTTATT | 11059 |
rs759057808 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396922 | TAAATTTTTTAGAGA[C/T]TAGATCTCACTGTGT | 11059 |
rs759068809 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441941 | TATCTAGTTGGATTT[C/T]GCATATTGGACTTTA | 11059 |
rs759089340 | in-del | -/AGG | 1.6477e-05 | 0.00287024 | cds-indel, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461298 | CTGCCGTTTACCTCT[-/AGG]AGGATTTGCTGAGCT | 11059 |
rs759115312 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465851 | ATATCTTTAACTTCA[C/T]TTAAAATACAAAGAA | 11059 |
rs759127307 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433231 | TTTTCCTAAGCCTCT[-/T]TTTTTTTTTTTTTTT | 11059 |
rs759139645 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401155 | TTCTGGGGTATAATA[C/T]TTAGCTTTTTTTGAT | 11059 |
rs759149555 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457303 | TAATAGGAGGTTAGT[A/C]TATTTTTTTATTTTC | 11059 |
rs759162700 | snp | C/T | 0.000183966 | 0.009589 | intron-variant | WWP1 | GRCh38.p7 | 8:86431393 | TAAATATTATACTCA[C/T]TTTATATTTCAGAAA | 11059 |
rs759168982 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394962 | AAAAAAAAAGCCAGG[A/G]GATGAGGGGGTTGGG | 11059 |
rs759200102 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356909 | TCCACAACTGTAAGC[A/C]TAAATTAAATTGTTC | 11059 |
rs759204723 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386851 | TTCTAGGATCTGGAA[A/G]TCCAAGATCAAGATG | 11059 |
rs759223873 | snp | A/G | 3.30131e-05 | 0.00406269 | intron-variant | WWP1 | GRCh38.p7 | 8:86431535 | TTGCATATATCAGTA[A/G]GTAGAACCAACCAAC | 11059 |
rs759240223 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443026 | TTTTAAATTTAAAAC[C/T]CATTTATAGTATGAC | 11059 |
rs759254229 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349807 | AGGACCCAAGAGTCC[A/G]TGCTGCTTGGAAGTA | 11059 |
rs759274246 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340851 | TATGTTTCAAAAGGG[C/T]TAAACTTGTTCATAC | 11059 |
rs759274687 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427546 | TTTAGTTATTTTAAC[A/G]TGTCTTGAACTTGAT | 11059 |
rs759295214 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429269 | TTCTGCCTATACCTC[A/G]TTGGCCAGAATTGGT | 11059 |
rs759365484 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376337 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACGT | 11059 |
rs759377599 | snp | A/G | 1.65111e-05 | 0.0028732 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442687 | TTGAGTATGCGGGCA[A/G]GAACAACTATTGTCT | 11059 |
rs759412876 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358481 | ACATTTATTGAGGAG[-/TT]TTTTTTTTTTTCCTT | 11059 |
rs759415071 | snp | A/C | | | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466664 | AGATTACTCTAAATA[A/C]TTCTGGCAAAATTTT | 11059 |
rs759421160 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371718 | TTATATATGTAGTTT[A/G]AATACTAATCTTTAA | 11059 |
rs759431081 | snp | C/T | 1.66131e-05 | 0.00288206 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466934 | TCTTGCATTTAAATA[C/T]CCCAGCCAAGAAAAA | 11059 |
rs759444197 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447752 | CACGATGGGGTTAGT[C/G]CTAAAAGCCTCACAG | 11059 |
rs759491080 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441848 | ATTACTGTAAGCATT[G/T]GAGTTTGGAACCCTT | 11059 |
rs759493580 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393991 | ACAAAGCCCTGTGGC[A/G]GGGCACTGAGGTCTC | 11059 |
rs759494186 | snp | A/C/G | 3.67183e-05 | 0.00428463 | intron-variant | WWP1 | GRCh38.p7 | 8:86435420 | TTCAACTTTATTATG[A/C/G]GTTAATTTGGTTTAT | 11059 |
rs759531162 | snp | C/T | | | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343142 | GGGTCACGGGTCTTG[C/T]CCGGAGTTCGCCCTG | 11059 |
rs759549299 | snp | A/G | 8.24328e-05 | 0.00641947 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411714 | ATTCCTTCTACCAGT[A/G]CAGAATTGGAATCTG | 11059 |
rs759576961 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363610 | AGTTCAAGACCAGCC[G/T]GGCCAACATGGTGAA | 11059 |
rs759592971 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438095 | CTGAGGCACCACACC[C/T]GGCCTGTATACTGTA | 11059 |
rs759678231 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421836 | TCAAAAAAAAAAAAT[A/T]TTTTTTGAAAATATA | 11059 |
rs759696287 | in-del | -/T | 0.00125646 | 0.025033 | intron-variant | WWP1 | GRCh38.p7 | 8:86402006 | GATTGAAATAAGGCA[-/T]TTTTTTTTCAAGGTT | 11059 |
rs759699894 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457960 | GTTGACTTGGCAGAT[A/T]GGCAGAGAAATACTG | 11059 |
rs759705335 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439081 | GGACGTGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 11059 |
rs759727780 | snp | A/T | 3.30207e-05 | 0.00406316 | intron-variant | WWP1 | GRCh38.p7 | 8:86398564 | TTTTTTTCTTTCTTG[A/T]TGTTCAGTAGAAATA | 11059 |
rs759751905 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396792 | AAAAATAGAGACAGC[A/G]TCTTGCTATGTTGGC | 11059 |
rs759754754 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419836 | CTAAATATTTTCAGC[A/G]ATTGAAAAAGCAGGT | 11059 |
rs759759294 | snp | G/T | 3.31917e-05 | 0.00407367 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411779 | TTCTAGAAGTAGTTC[G/T]GCTTTTGAAGCAGCC | 11059 |
rs759814789 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381765 | GTGATTGATTAACTT[C/T]GTGGCATTTTATGAA | 11059 |
rs759822447 | snp | C/T | 1.64939e-05 | 0.0028717 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398418 | TGGTGAATTGACAGT[C/T]GTGCTTGATGGATTG | 11059 |
rs759833865 | snp | C/T | 1.65996e-05 | 0.00288089 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380805 | TGTAGATGGAGAAAT[C/T]ACGAAAACAGCAAAA | 11059 |
rs759859991 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358545 | AGAGTGCAGTGGTGC[C/T]GTCACAACTCACCAC | 11059 |
rs759918842 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468471 | GACAGGTTATGTGAT[-/A]AGAGGGAAACTGGCC | 11059 |
rs759966657 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449559 | CTATTCTTAGCTCAA[A/T]TGCTGGACAAAAAAA | 11059 |
rs760001121 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360607 | ACCTTTGCCTCCAGA[A/G]TATATCTCTTTGCTG | 11059 |
rs760073633 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359318 | TATAAACAACTCTAA[C/G]AGTTTCATTGTTTCT | 11059 |
rs760094842 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412849 | TATTATTATTTTGGA[A/G]CAGAGTTTCATTCTT | 11059 |
rs760120064 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461909 | TTGTTTTGTTTTTTT[-/A]AAAAATATGTAAGAT | 11059 |
rs760136995 | snp | C/T | 1.65274e-05 | 0.00287462 | intron-variant | WWP1 | GRCh38.p7 | 8:86435577 | ATTTAGTCTTCTCTT[C/T]ATACAATACATATAC | 11059 |
rs760220595 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349337 | AACCAGATCTTCTTA[A/C]GGTTTAGACTTGTAA | 11059 |
rs760242384 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363453 | GGAGCTTAGTCCAAA[A/G]ACAATGGCTTCCCAT | 11059 |
rs760244899 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415805 | TTTATTATTTTTCTA[A/G]CACTTAAATTATGTG | 11059 |
rs760246022 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423894 | GGCGGCTGGCCGGGC[A/G]GGGGCTGCCCCCCAC | 11059 |
rs760268706 | snp | A/G | 3.75672e-05 | 0.00433384 | intron-variant | WWP1 | GRCh38.p7 | 8:86402251 | AGGAAAAGTAAATGA[A/G]GTTTATGTATCCATC | 11059 |
rs760295743 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417192 | GAGAATGTTGTCAGC[A/T]GCGGGAACTGGGTAC | 11059 |
rs760296153 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399946 | GTTCATTCAACAGAT[A/G]GTTACTTAATGCCTG | 11059 |
rs760326017 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368892 | TACTTTACCTTTTGC[A/G]TCTATTTTAGGAATT | 11059 |
rs760345148 | snp | C/G | 1.65551e-05 | 0.00287702 | intron-variant | WWP1 | GRCh38.p7 | 8:86431787 | AATATTGCTTAGTGA[C/G]CACATGAGATTTAGT | 11059 |
rs760345631 | snp | A/G | 3.30518e-05 | 0.00406507 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411574 | TTGCACCAACTGATA[A/G]TGCGTCTGTCACGGG | 11059 |
rs760349125 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400876 | TAACCAGGAGAGTGA[C/T]GTGATGACCTGGTTT | 11059 |
rs760355525 | snp | A/C | | | downstream-variant-500B, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468688 | AAATTACGATGCACT[A/C]GGTGAGGCTACACAG | 11059 |
rs760385716 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462104 | TAAGATGTAAGTATT[-/C]CCTGTTTTTTATGAA | 11059 |
rs760388474 | in-del | -/AA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400756 | TTTTTGATATTCAGT[-/AA]AATCGATTATCTGCT | 11059 |
rs760420386 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459935 | TGTTCTGATGAAATA[C/T]GTGCCTCAGCACAAT | 11059 |
rs760432505 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444972 | GTGCAGGCTGTACAA[G/T]AAGCATGGTGCCAGC | 11059 |
rs760442233 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364676 | CCAGGCATGGTGGTG[C/T]GTGCCTGTAGTGTCA | 11059 |
rs760442739 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407368 | CACATAGGTATCAGA[G/T]TTTCTCAATTTCAGC | 11059 |
rs760462031 | snp | A/C | 1.65877e-05 | 0.00287986 | intron-variant | WWP1 | GRCh38.p7 | 8:86430694 | AATCTTTTCTCCAAT[A/C]AGGCTTCAATGTTAG | 11059 |
rs760513687 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390503 | CTGGAGACCAGCCCG[C/T]CCAACACGGCGAAAC | 11059 |
rs760526278 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427748 | TGTCCGAAATTTTGA[A/G]CAGTGGCAATCTCAG | 11059 |
rs760546362 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459220 | TTTGCATTTTTAGTA[G/T]AGACGGGGTTTCACC | 11059 |
rs760579564 | snp | A/C/G | 5.35359e-05 | 0.00517354 | intron-variant | WWP1 | GRCh38.p7 | 8:86448144 | TTTTCATTTTTCTTT[A/C/G]CAGGCACTATTTCAT | 11059 |
rs760619312 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445832 | TTATTTTTTAATGTT[A/T]TAACAAAAGCCATTC | 11059 |
rs760697544 | in-del | -/AAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386511 | GCGGGGTGTCTTGAC[-/AAT]GATGCAGGCCCTGTG | 11059 |
rs760730271 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392374 | CAATTTTGAGGCGGA[A/G]AGAACCACTTTAAAT | 11059 |
rs760730867 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447922 | TTTTATCATCCTATA[C/G]AGTTTTTGATATATG | 11059 |
rs760771250 | snp | C/T | 5.056e-05 | 0.00502767 | intron-variant | WWP1 | GRCh38.p7 | 8:86435753 | TGTCTCATTGTATTC[C/T]GTGCATCTAAAGAAA | 11059 |
rs760773219 | snp | C/G | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411729 | GCAGAATTGGAATCT[C/G]AAGCTAGAAGTATAT | 11059 |
rs760786879 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433230 | TTTTTCCTAAGCCTC[-/TT]TTTTTTTTTTTTTTT | 11059 |
rs760789622 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359023 | TAGTGGGAGAAACAT[C/G]TGGGAAGTCGTTGGT | 11059 |
rs760790027 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440668 | AGGGAAGTTTTCTTC[A/T]ATTATGTCTTTGAAT | 11059 |
rs760797123 | snp | A/T | 6.60764e-05 | 0.00574751 | intron-variant | WWP1 | GRCh38.p7 | 8:86461730 | TTGTCAGAAGAAAAA[A/T]GTTTAAAGGACCAGA | 11059 |
rs760843557 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450552 | TCTAAATAAAATTTC[A/T]CTATGTAAGATGTAT | 11059 |
rs760862734 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441234 | CTCTCACAAGACCTG[C/T]TCCATCCTCTTACCT | 11059 |
rs760865874 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412622 | TCAACTGTTGTAGCT[A/G]TTGAAACTGCACTTC | 11059 |
rs760876616 | snp | C/T | 0.000132026 | 0.00812377 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427808 | GTTTAACCAACGATA[C/T]CTCTATTCGGTAATT | 11059 |
rs760880230 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438538 | GTTTTGAAAGGAACT[C/T]GTACTGCATGTGAGT | 11059 |
rs760918738 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395675 | ATAGTGAAATGCGTA[A/C]TACCAAAGACAAATA | 11059 |
rs760919612 | snp | A/G | 0.000120292 | 0.00775447 | intron-variant | WWP1 | GRCh38.p7 | 8:86401977 | CATGAAATGTTGTTG[A/G]ATTATACTTAAATGA | 11059 |
rs760967369 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | WWP1 | GRCh38.p7 | 8:86435594 | TACAATACATATACT[A/G]TAACTCAGATGATAT | 11059 |
rs760967845 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418750 | TGGAGGTCAGAGATA[C/T]TGTCCTAAATCAGCA | 11059 |
rs760988893 | snp | A/G | 0.000287689 | 0.0119901 | intron-variant | WWP1 | GRCh38.p7 | 8:86448524 | ATTGGGTAAGGTGAT[A/G]TACCTTATTAAGCTT | 11059 |
rs761004663 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345122 | GAATGGAAAGGAAGA[A/G]AGGAAGTCGAATAGC | 11059 |
rs761027021 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345326 | AATTTCCATATGCGC[C/G]TATGCTTTGTGGATA | 11059 |
rs761050870 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349613 | ACAGGGAAAGCTGAG[G/T]CTAAAAAGTGCAAAT | 11059 |
rs761088295 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411445 | GTAGTTGCTTAGTCT[A/G]GATTAGGCTCTGAAT | 11059 |
rs761094748 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429770 | TTCTTCTCCCATTTC[A/G]TCTTCCCTCTATAGA | 11059 |
rs761119571 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382020 | TTTTATTATTATATA[A/G]TTAGTTTATTGTAAA | 11059 |
rs761128937 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371605 | TTCAACATTGTTTCA[C/T]GTTTGTTGGCCTTAG | 11059 |
rs761136994 | in-del | -/TGA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357386 | ATACTCTTTTCATTT[-/TGA]TGATAACTTTAAGGG | 11059 |
rs761159979 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425992 | CATACTCAGATTTCC[A/C]TTCCAGATTCAATTT | 11059 |
rs761202867 | in-del | -/AC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454552 | TTAATCTTTTTAAAA[-/AC]CATCGACTTCATTTT | 11059 |
rs761216213 | snp | A/T | 3.31472e-05 | 0.00407093 | intron-variant | WWP1 | GRCh38.p7 | 8:86381458 | TACTTATTAATAGAA[A/T]GACAACGTCTACTCC | 11059 |
rs761234925 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370374 | TTGGACTCTGTAGTT[A/G]TTGCTGTATCATAGA | 11059 |
rs761264441 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428559 | AATGTAAGTAACTTT[C/G]TCCAAAATCCTGCTG | 11059 |
rs761290731 | snp | A/G/T | 3.3344e-05 | 0.00408303 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411811 | AATCAAGACAGCCAG[A/G/T]TGGGTGTATGGATCC | 11059 |
rs761302757 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388947 | TGAAATAAAGATGAC[-/TT]TGTTGTTTTGATATG | 11059 |
rs761305046 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357682 | GTTTAATATCAGGGA[A/T]TCTGGATAAAAGTAG | 11059 |
rs761322468 | snp | A/G | 4.94376e-05 | 0.00497156 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427785 | CAATTGCAGGGAGCT[A/G]TGCAACAGTTTAACC | 11059 |
rs761329592 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426878 | AAGAAAGAAGGAGAG[C/G]CCGGGCATGGTGGCT | 11059 |
rs761342002 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391608 | ATGTTTTTGCAATAA[A/G]GAAGAGATTCCAGCA | 11059 |
rs761359679 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375234 | AAATACCATGTTTTA[A/G]TGTACTTTAGTAATT | 11059 |
rs761364401 | snp | A/T | 5.05438e-05 | 0.00502686 | intron-variant | WWP1 | GRCh38.p7 | 8:86448335 | AACCCATTTTGTTTC[A/T]TTTTGTTAATTAGTG | 11059 |
rs761369373 | in-del | -/TATTTATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352227 | TTTTTTATTTTTATT[-/TATTTATT]TATTTATTTTAAGAC | 11059 |
rs761409259 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433365 | AATTTTGCTTTCTAT[A/G]TTCAGCTGCTTATTG | 11059 |
rs761421877 | snp | C/T | 3.34079e-05 | 0.00408691 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380763 | AAAAAAGAACTGGTT[C/T]GGAACAGCAATATAT | 11059 |
rs761460642 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415678 | TGTGATTCTGAGGCA[A/G]TCAATATTCTAATTT | 11059 |
rs761476187 | snp | G/T | 3.31752e-05 | 0.00407265 | intron-variant | WWP1 | GRCh38.p7 | 8:86374146 | TTTATATTTAATATG[G/T]TGATTCCCTGATGAA | 11059 |
rs761476274 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411699 | GAAAACAATGAATGT[A/G]TTCCTTCTACCAGTG | 11059 |
rs761519845 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402727 | TAGAGGTCAGAACTT[C/T]TACTGAGCAAGTGCT | 11059 |
rs761529616 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461288 | TCACTGGAACCTGCC[A/G]TTTACCTCTAGGAGG | 11059 |
rs761540893 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380201 | CTGGTGCATGTTACA[A/T]TATGGATGAACCTCA | 11059 |
rs761546518 | snp | C/T | 3.42677e-05 | 0.00413916 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448171 | TCATGGAAAGTTTAT[C/T]GATACTGGTTTCTCT | 11059 |
rs761608913 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402101 | TGCTGCTCGTATGTA[A/G]TTAATGGAGACAACA | 11059 |
rs761652370 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351576 | CAAGTGATCCCCCCT[A/G]CCTCGACCTCCCATA | 11059 |
rs761675580 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443261 | GTATTTTTAGTTGAG[A/G]TGGGGTTTCATCATG | 11059 |
rs761702435 | in-del | -/GTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441625 | TGGGCTGAATCAGAG[-/GTT]TTGTTTCCCCTGTAG | 11059 |
rs761730245 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440684 | TTATGTCTTTGAATA[-/T]TTTTTTCTGTTCCAT | 11059 |
rs761771347 | in-del | -/GATGCCTTACATGAAAATGGA | 1.6492e-05 | 0.00287154 | cds-indel, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398591 | ATACAGGAAAATGGT[-/GATGCCTTACATGAAAATGGA]GATGCCTTACATGAA | 11059 |
rs761855368 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359236 | TGTGTATAAATAATC[A/G]ATTTGAATGACCAGG | 11059 |
rs761872936 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462693 | ACATCCTAGAGATAG[A/G]TGATTCTTTCAAGAG | 11059 |
rs761889708 | snp | A/G | 3.30699e-05 | 0.00406618 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430717 | AATGTTAGCTGCAGA[A/G]AATGACCCTTATGGA | 11059 |
rs761926760 | snp | C/T | 4.97154e-05 | 0.0049855 | intron-variant | WWP1 | GRCh38.p7 | 8:86381464 | TTAATAGAATGACAA[C/T]GTCTACTCCTGTATT | 11059 |
rs761928586 | snp | G/T | 1.73742e-05 | 0.00294734 | intron-variant | WWP1 | GRCh38.p7 | 8:86425195 | TAGTGTGTTGTCTCT[G/T]ACTGTTATTTTTGTA | 11059 |
rs761949618 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409587 | ACAATAGGCTGGGCA[C/T]AGTGGCTCATGCCTG | 11059 |
rs762052520 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411207 | TTCAGAGTTTAGATG[A/G]CCCATACAGACTTCC | 11059 |
rs762078463 | in-del | -/AAATA | 2.13099e-05 | 0.00326412 | intron-variant | WWP1 | GRCh38.p7 | 8:86448120 | TATTTTGCAAATTTT[-/AAATA]AAATTTTTCATTTTT | 11059 |
rs762103236 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86431606 | TGTGATTTTAACTTT[A/G]TCTTTTAGCTTACAG | 11059 |
rs762110404 | in-del | -/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453091 | ATATACCATCTTAAC[-/TA]TATTTTTAAGTGTTC | 11059 |
rs762119768 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347356 | AATTTCCAAAGTATG[G/T]GGCTAGTTAGTGGCC | 11059 |
rs762134075 | in-del | -/ATATATAT | 0.355205 | 0.226786 | intron-variant | WWP1 | GRCh38.p7 | 8:86430799 | GATATATATCTCTCC[-/ATATATAT]ATATATATATATATA | 11059 |
rs762147731 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341408 | GTGGAATGACACAGA[C/T]GTATATTTTCGAATG | 11059 |
rs762147933 | snp | C/T | 1.99902e-05 | 0.00316144 | intron-variant | WWP1 | GRCh38.p7 | 8:86438540 | TTTGAAAGGAACTTG[C/T]ACTGCATGTGAGTAT | 11059 |
rs762156170 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383380 | TCCACTTATCTGCCA[A/G]ATGATCTTCTAGGAA | 11059 |
rs762171006 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348419 | GACGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 11059 |
rs762179834 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358818 | CTGGCCCATTTATTA[G/T]TTAGTAGGGGCCAGA | 11059 |
rs762189964 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440154 | AGAAATGAGGAAATA[C/T]GGTATTTTTACAGTG | 11059 |
rs762193039 | snp | A/G | 0.000236423 | 0.0108699 | intron-variant | WWP1 | GRCh38.p7 | 8:86448303 | AGATTTTGTTTTGCA[A/G]TAAGTCATTTTTTTG | 11059 |
rs762229826 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466378 | AAGACAGGGATTTTA[A/G]TTTTCTTCACTGTAT | 11059 |
rs762234993 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400833 | AGATGGGATAAAGGT[A/G]TGGCTGATTTTCAAA | 11059 |
rs762259112 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384236 | CTGGGGAGTAAAACT[A/T]CAACATACGAATTTG | 11059 |
rs762262756 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360971 | GCAGCATTCAGGGTA[A/T]TTAGGTTGAGGAATG | 11059 |
rs762265865 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452871 | TGTTCTCTGAACCAT[A/G]TAATTCCATGAGCAC | 11059 |
rs762283634 | in-del | -/TCT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408348 | TTACGTGAATATAAG[-/TCT]TCAATTCAGTTGGAT | 11059 |
rs762288663 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439204 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 11059 |
rs762296936 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399781 | AAATGGGTTCTTTTA[A/C]CTAGACTTCTGAATC | 11059 |
rs762304864 | in-del | -/TTTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352228 | TTTTATTTTTATTTA[-/TTTA]TTTATTTATTTATTT | 11059 |
rs762313384 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459332 | TGAGCCACCATGCCC[A/G]GCTTTTCTTTCCTTT | 11059 |
rs762352025 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403256 | AACATGGAAAGAAGC[-/A]ATTCAGTAATTACAT | 11059 |
rs762360380 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382528 | ACATGGTGAAACCTC[A/G]CCTCTACTAAAAGTA | 11059 |
rs762378414 | snp | G/T | 1.65559e-05 | 0.00287709 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398374 | CAATTAAAACTTTCC[G/T]TGGAAAACAAGAATG | 11059 |
rs762379815 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347853 | CAAAATATATATAGA[-/T]TTGGGTATCCCTAAT | 11059 |
rs762428509 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425799 | AATTAATAAAGTTTT[C/T]ATTACATACTAAAAT | 11059 |
rs762441712 | snp | C/T | 1.65329e-05 | 0.0028751 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381571 | TTTAAAAGCAGATGC[C/T]TTATTAGGAAAAGCA | 11059 |
rs762444803 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457413 | GGGGGAGATCTATCT[A/G]TCTGTCTGTCTGTCT | 11059 |
rs762455715 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451291 | AGAGGGAGATTTTGG[G/T]ACAGGGAAAACAGCA | 11059 |
rs762475679 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428846 | CATAAAAAGTAATAC[A/G]TATAGCTTTGTTTTT | 11059 |
rs762482412 | snp | C/T | 2.69458e-05 | 0.00367045 | intron-variant | WWP1 | GRCh38.p7 | 8:86431378 | ATCCTAAATAGTTAT[C/T]AAATATTATACTCAC | 11059 |
rs762484613 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402035 | TTGGCTGTTGAAGGC[A/G]CGAATGGAATAGATA | 11059 |
rs762549568 | snp | C/T | 1.66333e-05 | 0.00288381 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448379 | TTCACCCAGAGATAA[C/T]AACATTGAAGAATGT | 11059 |
rs762555082 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444471 | GCAATATGATTGTTT[A/G]TAGAGTGAGTATGGA | 11059 |
rs762618492 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343785 | TTCTTTTTCTATTTG[A/G]TAAGTTTAACAAATT | 11059 |
rs762623502 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373702 | ATGCTTCTGCCATAT[A/G]TTAGGAGTTTCTACT | 11059 |
rs762629584 | snp | A/G | 1.70365e-05 | 0.00291855 | intron-variant | WWP1 | GRCh38.p7 | 8:86380902 | GGAAAATCTTCACAA[A/G]AAAGTGTATTTTTTG | 11059 |
rs762652862 | snp | A/G | 3.32624e-05 | 0.004078 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448505 | GGAGAACAAAGATGA[A/G]TATATTGGGTAAGGT | 11059 |
rs762662521 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421929 | TGGGGAAGGGAGGTA[A/G]AAGGAAAGAGTGCTG | 11059 |
rs762669912 | in-del | -/TTTG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396462 | TCTAGTTGTTTGTTT[-/TTTG]TTTGTTTGTTTGTTT | 11059 |
rs762682134 | snp | A/G | 6.65391e-05 | 0.00576759 | intron-variant | WWP1 | GRCh38.p7 | 8:86430755 | CACCAGGCTGGGGTA[A/G]GCTGTTTTTGCTAAT | 11059 |
rs762692901 | snp | C/T | 4.43341e-05 | 0.00470798 | intron-variant | WWP1 | GRCh38.p7 | 8:86438716 | GAAATAAGTATATCT[C/T]ATTGTATACAGGGAA | 11059 |
rs762734719 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453906 | TCTCTGCCTGCTTTG[A/G]GTGTGCTATTTTAAC | 11059 |
rs762748044 | snp | A/T | 1.66957e-05 | 0.00288922 | intron-variant | WWP1 | GRCh38.p7 | 8:86461893 | AAGCCACAGAGAATC[A/T]TTTGTTTTGTTTTTT | 11059 |
rs762804954 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371317 | TTGTTATTATGAAGA[A/G]TGCTTATACTTGGTA | 11059 |
rs762809855 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456357 | CTATTGAGACAAAGA[C/T]CTTATATCTGGAATA | 11059 |
rs762828577 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86435405 | ACTGAATACTAAATA[C/T]TCAACTTTATTATGA | 11059 |
rs762842114 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394557 | TTGAAGGAAATGAGC[-/A]AAGCAGTGGTAAGGA | 11059 |
rs762865329 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378467 | TTAACTCTCCCTACC[C/T]TCTCACAGGTGACTC | 11059 |
rs762870341 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368073 | TTTTGAACTGCATAT[C/T]CAAATGAAACTTGTA | 11059 |
rs762880587 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398413 | CAAACTGGTGAATTG[A/G]CAGTTGTGCTTGATG | 11059 |
rs762881388 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436697 | AATATTTAAGGATAA[A/G]TAATCCAAATACTGT | 11059 |
rs762905183 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | WWP1 | GRCh38.p7 | 8:86452687 | AATTAGAGGTTAGGC[C/T]CTTTTATTATGCTAT | 11059 |
rs762929747 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439139 | ATGATATCAGGAGAT[C/T]GAGACCATCCTGGCT | 11059 |
rs762936143 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418490 | GCTGCAGTCATTTGG[A/G]GGATGGTTAAGTGCA | 11059 |
rs762966512 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433934 | AGGAAAAAAAAAAAA[A/T]GTAGAATCATCCACA | 11059 |
rs763048409 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438970 | ATTTTGTTTTTTTAT[A/G]TAGTGTGGGCATCTT | 11059 |
rs763049109 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410296 | AACCTTTCTGAGCCT[-/G]GAGCCTTTAGGAGGG | 11059 |
rs763077452 | snp | C/G | 1.6617e-05 | 0.00288239 | intron-variant | WWP1 | GRCh38.p7 | 8:86425330 | CAGGGTAATATAGCA[C/G]TCTTTATGCATTTGT | 11059 |
rs763115694 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381025 | GTTAAATTTTTTTTT[A/T]AAGGGGAGGATGCAT | 11059 |
rs763135223 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440045 | AAACTTTTCCAGAAA[C/T]GAAACACTGCCTATC | 11059 |
rs763144832 | in-del | -/TATTTTTG | 1.72046e-05 | 0.00293292 | intron-variant | WWP1 | GRCh38.p7 | 8:86425201 | GTTGTCTCTTACTGT[-/TATTTTTG]TATTTTTATTAAAGG | 11059 |
rs763211012 | snp | C/T | 1.65422e-05 | 0.0028759 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442679 | TTGCTTATTTGAGTA[C/T]GCGGGCAAGAACAAC | 11059 |
rs763234755 | snp | C/T | 3.29919e-05 | 0.00406138 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411584 | TGATAATGCGTCTGT[C/T]ACGGGTACTCCAGTA | 11059 |
rs763244770 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374899 | AAAAATTTTTTTAGA[C/G]ACAGGGTCTCACTAT | 11059 |
rs763248454 | in-del | -/AG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462221 | TGAGAGTACTCTAAC[-/AG]AGAACAACTAACGGG | 11059 |
rs763252033 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361212 | TTAGTTTGGATGAGA[A/C]ATTATGGGCTTGGAG | 11059 |
rs763272387 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355371 | CCTCTCATCCTCAGC[G/T]CAGCTCCATGACTCT | 11059 |
rs763284623 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425200 | TGTTGTCTCTTACTG[C/T]TATTTTTGTATTTTT | 11059 |
rs763304978 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401449 | TCTGTGATCCTAGCT[A/G]ATCAAGAGGCTGAGG | 11059 |
rs763382713 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376310 | GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 11059 |
rs763407177 | snp | C/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431633 | ACAGAATGAAGAACC[C/G]CTGCCAGAAGGCTGG | 11059 |
rs763439842 | in-del | -/AAAGAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364828 | AAGAAAGAAAGAAAG[-/AAAGAA]AGAGAGAGAGAGAGA | 11059 |
rs763444138 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361610 | TTTTTAACCTGCTTA[G/T]GTTAGTCATCTCACC | 11059 |
rs763450141 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358478 | ACACATTTATTGAGG[-/A]AGTTTTTTTTTTTTT | 11059 |
rs763484699 | snp | C/T | 1.68812e-05 | 0.00290522 | intron-variant | WWP1 | GRCh38.p7 | 8:86427627 | ATTATTGTTTATTAT[C/T]GTTTACTTGTGGTAG | 11059 |
rs763497035 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387066 | TTAATCCCTTCCTAA[A/G]GACCCTAATTTTTAA | 11059 |
rs763523419 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415562 | AAGAAAGAAAAACAC[A/G]AGTCTTGAATGTACC | 11059 |
rs763525604 | snp | A/G | 4.95462e-05 | 0.00497701 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374112 | GAAGGTTGCAGTTAC[A/G]GGTAACTGGTAAGTT | 11059 |
rs763666039 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428909 | GGTGAACAGGGCAGA[A/G]TGAGGTAACAGATGT | 11059 |
rs763692029 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373947 | TTGAGAACTTCTTAG[C/T]TGATTTAAACAAGTA | 11059 |
rs763738186 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360888 | TCATATATAAGTTGA[C/G]TTCTAAGACTGAGAA | 11059 |
rs763788449 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372357 | TAGAGACAGGTTTTC[A/G]CCGTGTTGGCCAGGC | 11059 |
rs763797591 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430512 | GAACTCCTGGGCTTA[A/C]GTAATCCTCCCACCT | 11059 |
rs763835535 | in-del | -/AA/AAAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364835 | AAGAAAGAAAGAAAG[-/AA/AAAT]AGAGAGAGAGAGAGA | 11059 |
rs763856375 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461965 | GTAGTCAGAATTTCA[A/G]TTTTGAGAACAGATT | 11059 |
rs763869325 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413116 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCAGCTCT | 11059 |
rs763873164 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377523 | TTTTTTATTTTTAGC[A/G]TATTTACTCTTATCC | 11059 |
rs763885728 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460144 | TTGAAAATAACCAGT[C/G]AATGAAATAGATAAT | 11059 |
rs763930796 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436720 | AATACTGTATTGTCA[A/G]TTTTTGCCCAATGAA | 11059 |
rs763938528 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434286 | ATGGCCTTACAGGAT[A/C]TGACCCCTCTTATCT | 11059 |
rs763976853 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457427 | TGTCTGTCTGTCTGT[A/C]TGTCTATCTATCTAT | 11059 |
rs764000465 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365206 | AATAGTAAGAATTGG[G/T]TATTCATACTAACTT | 11059 |
rs764013039 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418664 | AATTCCCTTCCCTGC[A/G]GCCAGAACTTCTGCT | 11059 |
rs764055627 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350160 | TGAATAAGGTGCTGC[C/T]TCTCCTTTCCAAGAA | 11059 |
rs764068017 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403628 | TGTATTTTTACCCAA[A/G]GTTGGTGTTTGGGGA | 11059 |
rs764079468 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398441 | ATGGATTGGTGATTG[A/G]GCAAGAAAATATAAC | 11059 |
rs764084203 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419013 | ACAAGCCCCACCCAG[G/T]CACATAAAACTCCCA | 11059 |
rs764121351 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388084 | ATAGCCATACATGGC[C/T]GCTGGCTACTGTATT | 11059 |
rs764150672 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427757 | TTTTGAACAGTGGCA[A/G]TCTCAGCGGAACCAA | 11059 |
rs764176392 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390514 | CCCGTCCAACACGGC[A/G]AAACCCCGTCTCCAC | 11059 |
rs764179612 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355443 | AAGAATGCCAAAATA[C/T]TAAAAATTTTTGAAT | 11059 |
rs764186098 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382086 | AAAAATTTTCTATAA[-/T]TTTACTATCCAAGGA | 11059 |
rs764215672 | snp | A/G | 1.6591e-05 | 0.00288015 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380815 | GAAATTACGAAAACA[A/G]CAAAATCCAGTAGTT | 11059 |
rs764264459 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382467 | ACTTTGGGAGGCCAG[C/G]GTGGGCAGATCACTT | 11059 |
rs764301227 | snp | A/G | 8.01073e-05 | 0.00632829 | intron-variant | WWP1 | GRCh38.p7 | 8:86438535 | ATTGTTTTGAAAGGA[A/G]CTTGTACTGCATGTG | 11059 |
rs764315044 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430799 | GATATATATCTCTCC[-/AT]ATATATATATATATA | 11059 |
rs764317440 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369124 | TAGACCTAGTAATAC[A/G]TTGTCATAAAAAATA | 11059 |
rs764335062 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414103 | TTGTAGAGTGCAACC[C/T]GTTAATAGGTTATGA | 11059 |
rs764354459 | snp | A/C | 1.65138e-05 | 0.00287343 | intron-variant | WWP1 | GRCh38.p7 | 8:86435600 | ACATATACTATAACT[A/C]AGATGATATTATGAT | 11059 |
rs764386086 | snp | A/C | 5.07739e-05 | 0.00503829 | intron-variant | WWP1 | GRCh38.p7 | 8:86430774 | GTTTTTGCTAATGAT[A/C]TATAAGGGAGATATA | 11059 |
rs764390296 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397253 | CACTGAAGATCAGAT[G/T]GAAGTATTTGGCCTC | 11059 |
rs764422315 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410450 | TTATTTATATTAAAC[-/AT]GTTTTCTTTATAACA | 11059 |
rs764464478 | snp | C/T | 1.70035e-05 | 0.00291572 | intron-variant | WWP1 | GRCh38.p7 | 8:86448527 | GGGTAAGGTGATATA[C/T]CTTATTAAGCTTAAT | 11059 |
rs764473950 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457195 | CATATTTTACTATAC[C/G]TAAAATAATGTTCAT | 11059 |
rs764491710 | snp | A/G | 1.67388e-05 | 0.00289294 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431416 | TTCAGAAAAAAGAGT[A/G]GATTCAACAGACAGG | 11059 |
rs764503048 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361615 | AACCTGCTTATGTTA[A/G]TCATCTCACCTCTCT | 11059 |
rs764517290 | snp | A/G | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448404 | GAATGTGGCTTAGAA[A/G]TGTACTTTTCTGTTG | 11059 |
rs764521557 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358757 | CAATTAATCCACCCA[C/T]CTTGGCCTCCCAAGG | 11059 |
rs764532911 | snp | A/G | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452571 | CAGTTTAATGACAGA[A/G]TGGCGTTTTTCTCGA | 11059 |
rs764558194 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86347275 | ACAGGCGTGAGCCAT[C/T]GCTTCCAGCCAATCA | 11059 |
rs764558512 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397783 | ATAAAAATGATAAAC[A/G]ATTGTCACAATATGT | 11059 |
rs764578100 | snp | A/G | 4.97137e-05 | 0.00498542 | intron-variant | WWP1 | GRCh38.p7 | 8:86381462 | TATTAATAGAATGAC[A/G]ACGTCTACTCCTGTA | 11059 |
rs764601521 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349699 | GAAAAGAGGAGAACA[-/T]TTGTGGCCTCTGAGG | 11059 |
rs764621036 | snp | A/G | 3.29843e-05 | 0.00406092 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398611 | CCTTACATGAAAATG[A/G]AGAGCCTTCAGCAAG | 11059 |
rs764625424 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401174 | GCTTTTTTTGATCAT[A/C]CTGTAGTCATGATTT | 11059 |
rs764636473 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380924 | TATTTTTTGGAATAT[A/G]TTTTTTGTTTTGTAA | 11059 |
rs764680170 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456150 | ATTCATGCTTACAAT[G/T]AAAAAGAATTATAAG | 11059 |
rs764778118 | in-del | -/TTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433231 | TTTCCTAAGCCTCTT[-/TTT]TTTTTTTTTTTTTTT | 11059 |
rs764806923 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441950 | GGATTTCGCATATTG[C/G]ACTTTAAAATGGGTG | 11059 |
rs764808098 | snp | A/C | 1.65329e-05 | 0.0028751 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430725 | CTGCAGAAAATGACC[A/C]TTATGGACCTTTGCC | 11059 |
rs764809593 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386922 | CAAGATGGCACCTTG[G/T]TGCTGCATCCTCTGA | 11059 |
rs764829795 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426177 | TGCAATATAGCAAAC[A/C]ATGAAGTTCATTTTA | 11059 |
rs764836352 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448866 | TTTTAGAGAGAGTTT[C/G]ACTCTGTCGCTCAGG | 11059 |
rs764855573 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443086 | GAAAAAATTTTAATT[A/C]TTTTGAGAAAGGATC | 11059 |
rs764859361 | snp | C/T | 1.68326e-05 | 0.00290104 | intron-variant | WWP1 | GRCh38.p7 | 8:86448338 | CCATTTTGTTTCATT[C/T]TGTTAATTAGTGTAT | 11059 |
rs764859449 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427790 | GCAGGGAGCTATGCA[A/G]CAGTTTAACCAACGA | 11059 |
rs764893834 | in-del | -/T | 3.29848e-05 | 0.00406095 | intron-variant | WWP1 | GRCh38.p7 | 8:86461326 | GAGCTCATGGGTAAA[-/T]GTAATTTCACTGTAA | 11059 |
rs764912750 | snp | C/T | 2.00066e-05 | 0.00316274 | intron-variant | WWP1 | GRCh38.p7 | 8:86438542 | TGAAAGGAACTTGTA[C/T]TGCATGTGAGTATTT | 11059 |
rs764928613 | snp | C/T | 1.6996e-05 | 0.00291508 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448195 | TTTCTCTTTACCATT[C/T]TACAAGCGTATGTTA | 11059 |
rs764934041 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349792 | GATCTAACAAAGTAC[A/G]GGACCCAAGAGTCCA | 11059 |
rs764997576 | snp | G/T | 3.3399e-05 | 0.00408637 | intron-variant | WWP1 | GRCh38.p7 | 8:86427636 | TATTATTGTTTACTT[G/T]TGGTAGTTGGGAAAG | 11059 |
rs765043590 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | WWP1 | GRCh38.p7 | 8:86461750 | AAAGGACCAGATAAA[C/T]TTTGTCTTATTTTCT | 11059 |
rs765068878 | in-del | -/AGAAGATGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86365060 | TTATGTTACTGGAAA[-/AGAAGATGT]AAAAATTAGAGAGTA | 11059 |
rs765075953 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447788 | AGTGAGAGTAAGAAA[C/T]GAACGAGAGAGCTGC | 11059 |
rs765077772 | in-del | -/GA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377017 | CCTTGGGTTAATAAT[-/GA]GAAACCAACTGAGGT | 11059 |
rs765094785 | snp | A/C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461311 | CTAGGAGGATTTGCT[A/C/G]AGCTCATGGGTAAAT | 11059 |
rs765100613 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433798 | TGGCGTGTGCCTGTA[A/G]TCCCAGCTACTCAGG | 11059 |
rs765108181 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416109 | ATTGAACTTAATTAC[A/G]AAGAGTTTATTTATT | 11059 |
rs765130847 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434882 | CCTGTCAGGCCCTCA[A/G]TCAATAGGCAAGAGA | 11059 |
rs765150942 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341373 | GAGAGCTCCGAAAAG[C/T]CAAAGAATGATTTTA | 11059 |
rs765217021 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363631 | ACATGGTGAAACCCC[A/G]TCTCTACGAAAAATA | 11059 |
rs765241341 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462195 | CCTGGGAAGTCCTTC[A/G]AAGGGAAAAATGAGA | 11059 |
rs765269062 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380697 | CTTTTTGGCAACACA[A/T]ACTCACTAGTGAATT | 11059 |
rs765275297 | in-del | -/G | 1.64972e-05 | 0.00287199 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402041 | GTTGAAGGCACGAAT[-/G]GAATAGATAATCATG | 11059 |
rs765277551 | snp | A/G | 4.97269e-05 | 0.00498608 | synonymous-codon, missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402019 | CATTTTTTTTTCAAG[A/G]TTGGCTGTTGAAGGC | 11059 |
rs765320455 | in-del | -/CTGGATAAATTATTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457275 | CTAGAGAATATTATT[-/CTGGATAAATTATTA]ATAGGAGGTTAGTAT | 11059 |
rs765357577 | snp | A/C | 3.88041e-05 | 0.0044046 | intron-variant | WWP1 | GRCh38.p7 | 8:86452516 | TTAAGTATTTTACTT[A/C]ACATATAAATTACCT | 11059 |
rs765357652 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379140 | GGAAATATATGAGCA[C/G]TTTTATTCAAAGAAT | 11059 |
rs765371534 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429919 | AACTTAGTGTCTTGG[C/G]TGGGAGCGGTGGCTT | 11059 |
rs765377339 | in-del | -/TCT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383385 | TTATCTGCCAAATGA[-/TCT]TCTAGGAAGGTTGTA | 11059 |
rs765382851 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421849 | ATTTTTTTTGAAAAT[A/G]TAAATTTACCATATT | 11059 |
rs765396284 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366920 | ATTTAAAATTAAGTC[C/G]TCTATTTTGTAGTTT | 11059 |
rs765407112 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396842 | TGGGCTCAAGTGATG[C/T]GCCTGCCTCACCTCC | 11059 |
rs765437497 | snp | A/G | 1.67172e-05 | 0.00289108 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411823 | CAGATGGGTGTATGG[A/G]TCCTGTACGGCAGCA | 11059 |
rs765448297 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353668 | GCTAATTTTTGTAGA[C/G]ATGGGGGTTTCACCA | 11059 |
rs765486529 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428762 | ATCTGTGGTAAGGTT[C/T]CATAATTTAGCTGTA | 11059 |
rs765565606 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | WWP1 | GRCh38.p7 | 8:86411492 | TTAGGTAATTGATTG[C/T]TTTATCATTACTTGA | 11059 |
rs765568542 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359376 | AGAAAAGTCTTGCCT[A/G]TGGGGATTGGTGCCA | 11059 |
rs765599777 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459235 | GAGACGGGGTTTCAC[C/G]ATGTTGGCCAGGCTG | 11059 |
rs765606928 | snp | C/T | 4.94686e-05 | 0.00497311 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452661 | GTGGCTACAGTACTT[C/T]GATGAAAAAGAATTA | 11059 |
rs765624718 | snp | A/C | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431631 | TTACAGAATGAAGAA[A/C]CCCTGCCAGAAGGCT | 11059 |
rs765648415 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463859 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 11059 |
rs765675546 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350489 | CCTAATGCAAATCTC[-/TT]TGCAAATTTCTGAAA | 11059 |
rs765679738 | snp | A/G | 1.66183e-05 | 0.00288251 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431431 | GGATTCAACAGACAG[A/G]GTTTACTTTGTGAAT | 11059 |
rs765701212 | in-del | -/TCTGTCTG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457410 | TTTGGGGGAGATCTA[-/TCTGTCTG]TCTGTCTGTCTGTCT | 11059 |
rs765715341 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412884 | GCCAGGCTAGAGTGC[A/G]ATGGCACGATCTTGG | 11059 |
rs765731814 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360615 | CTCCAGAATATATCT[A/C]TTTGCTGTGCTGTGT | 11059 |
rs765768322 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396087 | GAGAAAGCTGAAATT[C/T]GTGCTTTTGTAGTTT | 11059 |
rs765769052 | in-del | -/AA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395489 | CATACTGTCCCAAAC[-/AA]AAGAGAGCAAAGAGA | 11059 |
rs765771211 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453007 | ATTTTAAGTCATGAG[A/T]TCTTAGTGGTCTTAA | 11059 |
rs765775270 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415840 | ACAGTGTTATTATCT[C/G]TTGTCTCTCCACTAG | 11059 |
rs765784930 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345570 | GCTTGCCACCACACC[C/G]GGCTAATTTTTGTAT | 11059 |
rs765795557 | in-del | -/GC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396423 | TTTTTGTGTGTGTGT[-/GC]GCTTTCGTATTTCCT | 11059 |
rs765804394 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467475 | AATAAATACAATAGT[C/T]GAAAATTTTTCTCTG | 11059 |
rs765812374 | in-del | -/AAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364830 | AAAGAAAGAAAGAAA[-/AAAA]GAAAGAGAGAGAGAG | 11059 |
rs765834745 | snp | G/T | 3.83936e-05 | 0.00438125 | intron-variant | WWP1 | GRCh38.p7 | 8:86431390 | TATTAAATATTATAC[G/T]CACTTTATATTTCAG | 11059 |
rs765846340 | in-del | -/TTTAAC | 1.65026e-05 | 0.00287246 | intron-variant | WWP1 | GRCh38.p7 | 8:86431597 | GGTTCATCTTGTGAT[-/TTTAAC]TTTATCTTTTAGCTT | 11059 |
rs765866782 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425100 | TTATATATATAGCTG[-/TG]TGTGTGTGTATAGTC | 11059 |
rs765890322 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372478 | TTGGTTAGTATGCCC[C/G]TGTCTCTTAAGAAAT | 11059 |
rs765922832 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454366 | TTGAATCTGCTGATA[C/T]GAAAGCTGTTGGATA | 11059 |
rs765932663 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417211 | GGAACTGGGTACACA[A/C]CATGCCCACAACCCG | 11059 |
rs765960618 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383260 | TAAGTATACAGTACC[C/T]TGCCTGGATTATTAT | 11059 |
rs765961795 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402128 | AACACACCTTCATCT[C/T]CGTCTCAGGTTGCTG | 11059 |
rs765977574 | in-del | -/TTC/TTCTTTTC/TTTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445978 | TTCTTTTCTTTTCTT[-/TTC/TTCTTTTC/TTTT]TTTTTTTTTTTTTTT | 11059 |
rs765994357 | snp | C/T | 1.66521e-05 | 0.00288544 | intron-variant | WWP1 | GRCh38.p7 | 8:86430757 | CCAGGCTGGGGTAAG[C/T]TGTTTTTGCTAATGA | 11059 |
rs766014902 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348532 | CGTCTTGACATTTCT[G/T]AAATCTACAGTTCAC | 11059 |
rs766015937 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402036 | TGGCTGTTGAAGGCA[C/T]GAATGGAATAGATAA | 11059 |
rs766057304 | snp | C/T | 3.42161e-05 | 0.00413605 | intron-variant | WWP1 | GRCh38.p7 | 8:86425203 | TGTCTCTTACTGTTA[C/T]TTTTGTATTTTTATT | 11059 |
rs766061249 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355623 | GAATGCTTTCCCAGA[A/G]TACGTGGAAATTATG | 11059 |
rs766074157 | in-del | -/AG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364829 | GAAAGAAAGAAAGAA[-/AG]AGAAAGAGAGAGAGA | 11059 |
rs766102605 | snp | A/T | | | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411569 | CTCATTTGCACCAAC[A/T]GATAATGCGTCTGTC | 11059 |
rs766179741 | snp | C/G | 6.81361e-05 | 0.00583639 | intron-variant | WWP1 | GRCh38.p7 | 8:86438720 | TAAGTATATCTCATT[C/G]TATACAGGGAAAGTA | 11059 |
rs766218565 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355321 | TTTGGCCTGCCATTA[A/G]GAAGCTCTGTGTTTC | 11059 |
rs766234646 | snp | A/T | 1.80461e-05 | 0.00300379 | intron-variant | WWP1 | GRCh38.p7 | 8:86438580 | ATGTTTTTGTTTTTA[A/T]TTAGATTATGGCATT | 11059 |
rs766234983 | snp | C/T | 1.66944e-05 | 0.0028891 | intron-variant | WWP1 | GRCh38.p7 | 8:86461895 | GCCACAGAGAATCTT[C/T]TGTTTTGTTTTTTTA | 11059 |
rs766240464 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391857 | GCCCTATCCTTCCCA[A/G]TGATTGCATTTTAAA | 11059 |
rs766272239 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465810 | AAGGGGAGGGCAGTA[C/T]ATGGTCTGCTTAGTT | 11059 |
rs766280460 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433671 | GAAATCACCTTGTTA[C/T]GGTGGCTCACGCCTA | 11059 |
rs766362220 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457925 | TCATTTCCCAGGTTA[C/T]GTTGTGTGGCATGCA | 11059 |
rs766385662 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345691 | TGCTGGGATTACAGC[A/G]TAAGCCACCCTGCCG | 11059 |
rs766415434 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395789 | TAGTGGAAAAATATC[G/T]TCAAAGAGTTGAGAT | 11059 |
rs766425908 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362369 | CCACATCAGTGTTTA[C/T]TGAGTGATTGAATTG | 11059 |
rs766473870 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431642 | AGAACCCCTGCCAGA[A/G]GGCTGGGAAATTAGA | 11059 |
rs766474154 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394373 | AAGTTCCCCTAGGAC[A/G]GGACTACCTTAATCA | 11059 |
rs766497701 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361227 | AATTATGGGCTTGGA[A/G]ATAAGAGTTGTAGTG | 11059 |
rs766498005 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401478 | GGCAGGAGGATTACT[G/T]GAGCCTAAGAGGTTG | 11059 |
rs766510315 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341155 | ATACCTACGGAATTT[A/C]TGAGGACGTGTTTGT | 11059 |
rs766526469 | snp | C/G | 1.64917e-05 | 0.00287151 | intron-variant | WWP1 | GRCh38.p7 | 8:86452688 | ATTAGAGGTTAGGCC[C/G]TTTTATTATGCTATT | 11059 |
rs766528425 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427872 | TCAGGTGTTTCTTTC[-/T]TTTTTTTTTTTTGCT | 11059 |
rs766565032 | snp | A/G | 3.39184e-05 | 0.00411802 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381613 | GAAACAAGCTCTGTT[A/G]ATACACAATAGAAAA | 11059 |
rs766566785 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418801 | AGGTTAGTAAGTGAA[A/G]AAGGTTGTAAAGTAA | 11059 |
rs766665438 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363865 | AGGTATTTATTCTGT[A/G]CCAGGAAGTATTTTT | 11059 |
rs766679686 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437925 | CTGCCTTAGCCTCCC[A/G]AATAGCTGGGACTAC | 11059 |
rs766705606 | snp | C/G | 1.65943e-05 | 0.00288043 | intron-variant | WWP1 | GRCh38.p7 | 8:86374148 | TATATTTAATATGGT[C/G]ATTCCCTGATGAACT | 11059 |
rs766705930 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370562 | ACTCTTGAGGCTCAG[C/G]ATCCACAGTACCCCA | 11059 |
rs766706200 | snp | C/T | 0.000376223 | 0.0137102 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468391 | GACTCCTTTTCCAAA[C/T]CCTTATTATGAACAC | 11059 |
rs766728076 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384481 | GGTTGTGATTAAAAC[A/T]TAAGTTTTCTGATTC | 11059 |
rs766734572 | snp | A/G | 1.85496e-05 | 0.0030454 | intron-variant | WWP1 | GRCh38.p7 | 8:86435417 | ATATTCAACTTTATT[A/G]TGAGTTAATTTGGTT | 11059 |
rs766757245 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357686 | AATATCAGGGATTCT[A/G]GATAAAAGTAGCTAT | 11059 |
rs766760701 | snp | A/G | 3.29799e-05 | 0.00406065 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411587 | TAATGCGTCTGTCAC[A/G]GGTACTCCAGTAGTG | 11059 |
rs766794992 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407842 | TTGTATTACTAACAT[C/T]TTGCATTACTGTGAT | 11059 |
rs766811841 | snp | C/T | 7.20526e-05 | 0.00600176 | intron-variant | WWP1 | GRCh38.p7 | 8:86411503 | ATTGCTTTATCATTA[C/T]TTGATAGATGATTTT | 11059 |
rs766813425 | in-del | -/AGAC | 1.64851e-05 | 0.00287093 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461234 | TACAGTTTGTGAAAG[-/AGAC]AGACAATGAAGTAAG | 11059 |
rs766826649 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426022 | TAAAGCCCACCATTT[C/T]AAAACACATTCAAAA | 11059 |
rs766854576 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462107 | GATGTAAGTATTCCC[C/T]GTTTTTTATGAAGTT | 11059 |
rs766872161 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371737 | ACTAATCTTTAATTA[C/G]TTTTTTGTTTCGCAA | 11059 |
rs766885022 | in-del | -/GTTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386064 | CCGAGTCTTAGTTCA[-/GTTT]GTCTAATTTCCTGCT | 11059 |
rs766925099 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359186 | CATCTTTTTTTCTCT[A/C]CCTAAATTTTAATGA | 11059 |
rs766929883 | snp | G/T | 0.000168591 | 0.00917972 | intron-variant | WWP1 | GRCh38.p7 | 8:86440641 | GAATATATTAAGATC[G/T]TCCTTAATGTCAGGG | 11059 |
rs766932058 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373971 | ACAAGTAGTTTTAAT[A/G]TCTTGAAAATTACAA | 11059 |
rs766966967 | in-del | -/CAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455201 | AAAGGGAATCATCAT[-/CAA]CAACAAAAAACCTCA | 11059 |
rs766984847 | snp | A/C | 1.74851e-05 | 0.00295673 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466752 | TATTAGATTTTTTTC[A/C]TTTTATTGAAAACAT | 11059 |
rs767008274 | snp | C/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341660 | AATTTAGGACCTAAT[C/G]TTAAAACGTGATTAT | 11059 |
rs767018568 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343987 | TAACAAGAGTTCATG[-/T]TTATGTGTAAATCCA | 11059 |
rs767036351 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346210 | CAGTTAGCAATATCA[A/G]ATCATTCATTTGGAT | 11059 |
rs767044765 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371988 | GCTGAGACTGCAGGC[G/T]CCCACCACCACGCCT | 11059 |
rs767049925 | snp | A/C | 1.66145e-05 | 0.00288218 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466935 | CTTGCATTTAAATAC[A/C]CCAGCCAAGAAAAAT | 11059 |
rs767158285 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362002 | TATATACATATATAT[A/G]CACACATATATATAT | 11059 |
rs767226203 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459176 | AAGTAGTTGGGATTA[C/T]GGGTGTGCGCCACCA | 11059 |
rs767281746 | snp | G/T | 1.64939e-05 | 0.0028717 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398419 | GGTGAATTGACAGTT[G/T]TGCTTGATGGATTGG | 11059 |
rs767301057 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457550 | TACATAATAGATACA[C/T]ACACACATTTAGATA | 11059 |
rs767321145 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452880 | AACCATATAATTCCA[G/T]GAGCACAAAATCATC | 11059 |
rs767334816 | snp | A/C | 6.7714e-05 | 0.00581828 | intron-variant | WWP1 | GRCh38.p7 | 8:86425364 | TATATTTTATCACAC[A/C]TGTGGTTTTTAAATT | 11059 |
rs767360695 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443317 | GAGCTGAAGTGATCC[G/T]CCTGTCTCGGCCTCC | 11059 |
rs767403717 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351580 | TGATCCCCCCTACCT[C/T]GACCTCCCATAGTGC | 11059 |
rs767405269 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | WWP1 | GRCh38.p7 | 8:86452707 | TATTATGCTATTGTA[A/G]GGAATGTTAGTGGGG | 11059 |
rs767425285 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387792 | GCCTCTGAAAGTGCC[A/G]GGATTATAGGCATGA | 11059 |
rs767432291 | snp | A/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442709 | CTATTGTCTGCAGAT[A/T]AATCCAGCATCAACC | 11059 |
rs767512952 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429047 | TGACTCAGTAGTGTC[A/G]TCAAGGACCCGGGTT | 11059 |
rs767518341 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411297 | CTTAAGGTTGTTATT[A/G]TTATACATACTTAAA | 11059 |
rs767535767 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412082 | GACATATATGTAGTA[C/T]GAAGGGAAAAGAAAA | 11059 |
rs767543646 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461988 | AACAGATTAATACAG[C/T]ATTCTATAACTGAAC | 11059 |
rs767569800 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341186 | AAGCACATTATTGCA[G/T]CTATTTAAAGGGACC | 11059 |
rs767599555 | snp | C/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411597 | GTCACGGGTACTCCA[C/G]TAGTGTCTGAAGAAA | 11059 |
rs767606284 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341459 | CACCAATTTCAACTA[C/T]GAAGCCAGAGGACAA | 11059 |
rs767672547 | snp | A/T | 3.30595e-05 | 0.00406554 | intron-variant | WWP1 | GRCh38.p7 | 8:86435578 | TTTAGTCTTCTCTTT[A/T]TACAATACATATACT | 11059 |
rs767697853 | snp | A/C | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341102 | GAAGAGGAGGCCTGC[A/C]TGCATTCTGGAGAAG | 11059 |
rs767698794 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436477 | CCAGCCATTTATGGT[-/G]CTTTATTCTTTTTCA | 11059 |
rs767726159 | snp | A/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461249 | AGACAGACAATGAAG[A/T]AAGAATGCGACTATT | 11059 |
rs767766899 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357297 | GTGTTTTCTAAACTG[A/G]TGACTCTTGGAGGGA | 11059 |
rs767767874 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399816 | ATTCTTGCTGGTTGG[A/C]TGGGGAGGGGTATAC | 11059 |
rs767773883 | snp | C/T | 4.9807e-05 | 0.00499009 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380807 | TAGATGGAGAAATTA[C/T]GAAAACAGCAAAATC | 11059 |
rs767779129 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457977 | GCAGAGAAATACTGT[G/T]TATCGACATTATACA | 11059 |
rs767796901 | snp | A/G | 1.64985e-05 | 0.0028721 | missense, splice-acceptor-variant, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398574 | TCTTGTTGTTCAGTA[A/G]AAATACAGGAAAATG | 11059 |
rs767812686 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382614 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 11059 |
rs767817046 | snp | A/G | 3.40032e-05 | 0.00412316 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448203 | TACCATTCTACAAGC[A/G]TATGTTAAGTAAAAA | 11059 |
rs767878132 | snp | A/G | 1.71314e-05 | 0.00292667 | intron-variant | WWP1 | GRCh38.p7 | 8:86380906 | AATCTTCACAAGAAA[A/G]TGTATTTTTTGGAAT | 11059 |
rs767909098 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86381190 | TATAGTAAAAGTATC[A/G]TGTAAGTCTTTAGAC | 11059 |
rs767916117 | in-del | -/ATATATATA | 0.0253123 | 0.109615 | intron-variant | WWP1 | GRCh38.p7 | 8:86430801 | TATATATCTCTCCAT[-/ATATATATA]TATATATATATATAT | 11059 |
rs767916965 | in-del | -/T | 1.65293e-05 | 0.00287479 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448429 | CTGTTGACATGGAGA[-/T]TTTGGGAAAAGTTAC | 11059 |
rs767919094 | snp | G/T | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448398 | ATTGAAGAATGTGGC[G/T]TAGAAATGTACTTTT | 11059 |
rs767938504 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348444 | GCTGGTCTTGAACTC[C/G]AGACCACAGGTGATC | 11059 |
rs767947381 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439215 | AGGCGTGGTGGTGGG[C/T]GCCTGTAGTTCCAGC | 11059 |
rs767958695 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355835 | AACTTCAGATTGATA[C/T]AGCAAACTTCTCATT | 11059 |
rs767964384 | snp | C/T | 3.29821e-05 | 0.00406078 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411720 | TCTACCAGTGCAGAA[C/T]TGGAATCTGAAGCTA | 11059 |
rs768002537 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440208 | TTATCTGAGCCCTTA[C/T]TTGCCTCAACTATTT | 11059 |
rs768031066 | in-del | -/TGGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396519 | CTATGGTGCTACAAA[-/TGGT]TGGGGTATTCTATAA | 11059 |
rs768042837 | in-del | -/TTGT | 3.41047e-05 | 0.00412931 | intron-variant | WWP1 | GRCh38.p7 | 8:86427616 | TATATTGAGAGATTA[-/TTGT]TTATTATTGTTTACT | 11059 |
rs768052525 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459949 | ATGTGCCTCAGCACA[A/G]TTCTTCACTGAAATA | 11059 |
rs768121866 | snp | A/C | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368670 | CAGTTTAGACCCTCT[A/C]TGTTTGCCTGATCAC | 11059 |
rs768123692 | snp | G/T | 1.6659e-05 | 0.00288604 | intron-variant | WWP1 | GRCh38.p7 | 8:86374166 | TCCCTGATGAACTTT[G/T]CTTTTGAATACCTAA | 11059 |
rs768129530 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425836 | TATTAGGCTGTCATT[C/G]AAGGCCATTCACAAA | 11059 |
rs768145496 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355599 | AGAGTGAGAATGTCA[C/T]GTTGTCCTGAATGCT | 11059 |
rs768162177 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458830 | TAGACACTTCTAGAA[A/C]TTTATCTTAAAATAT | 11059 |
rs768276034 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421748 | AGAATGGTGTGAACC[C/T]GGGAGGCGGAGCTTA | 11059 |
rs768278104 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405434 | ACTGTGCATATCTCT[A/G]CATTTCGCTGCAGAA | 11059 |
rs768282811 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352979 | TAGAAGTTATGATTC[A/G]TTATTAAATAGTCTG | 11059 |
rs768318109 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450455 | GTTAAGCCTGAGCCT[C/T]CCACAAAGTCCAACA | 11059 |
rs768322394 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413515 | GGAGTTACCTGCGCC[A/G]TTGACGTCAAAGAAT | 11059 |
rs768342604 | snp | A/G | 1.65589e-05 | 0.00287736 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430703 | TCCAATCAGGCTTCA[A/G]TGTTAGCTGCAGAAA | 11059 |
rs768357613 | snp | A/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445621 | CTGTGGGGAACATAC[A/G/T]GTGCTTGTGTCCTTT | 11059 |
rs768360687 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392224 | AGATTGAGGCCTAGT[A/C]AAGAAGGTCCTGAGG | 11059 |
rs768369343 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437757 | AGAGTCAGTTAACAC[A/G]TAGAGTCAGTTAACA | 11059 |
rs768382742 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408570 | ACTGAATCTTCCCAT[A/T]GAGAGATATTTTATG | 11059 |
rs768405246 | in-del | -/CGA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400761 | GATATTCAGTAAAAT[-/CGA]TTATCTGCTGCAAAG | 11059 |
rs768425206 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395476 | TGAGTCCACAGATTC[A/G]TACTGTCCCAAACAA | 11059 |
rs768481238 | in-del | -/T | 3.30677e-05 | 0.00406605 | intron-variant | WWP1 | GRCh38.p7 | 8:86398548 | TATATAAAAACCTAG[-/T]TTTTTTTCTTTCTTG | 11059 |
rs768488474 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378476 | CCTACCCTCTCACAG[G/T]TGACTCATTTTCTGA | 11059 |
rs768514303 | snp | A/G | 6.75436e-05 | 0.00581096 | intron-variant | WWP1 | GRCh38.p7 | 8:86380891 | GTGTAAAGGACGGAA[A/G]ATCTTCACAAGAAAG | 11059 |
rs768520644 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421606 | GAGGCGGAAGGATCA[C/T]GAGGTCAGCAGTTTG | 11059 |
rs768542140 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380044 | AACATACGTCCACAA[A/G]AAAGCCTGTGCACAA | 11059 |
rs768574453 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450445 | TTCTATATTTGTTAA[A/G]CCTGAGCCTTCCACA | 11059 |
rs768579597 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384826 | GGCAACATGGTGAAA[-/C]CCCATCTCTACCAGA | 11059 |
rs768580133 | snp | G/T | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448463 | ACATGACCTGAAGTT[G/T]GGAGGTTCCAATATT | 11059 |
rs768606158 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400475 | TTTTTAAAAGAGATG[C/T]CAAGGAATCATCTCT | 11059 |
rs768629119 | snp | A/G/T | 3.32172e-05 | 0.00407526 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402179 | GCTCCAAAACCACTC[A/G/T]CATCTGAGCCTGCCG | 11059 |
rs768652790 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367738 | AACCTAAATTGATCA[C/T]ATAGTTTTTCTGTCT | 11059 |
rs768653240 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461844 | ACCAAGAAGCCATAC[A/G]TGGTAAGTTCAAGAA | 11059 |
rs768657995 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419508 | CCCAATGCTATAAAA[A/G]TGGAATACTCAAAGG | 11059 |
rs768709416 | in-del | -/CTT | 0.000165489 | 0.00909489 | cds-indel, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466900 | CAAGAATGAATGTGG[-/CTT]CTTATTTTGGAGGAG | 11059 |
rs768730517 | in-del | -/TCTA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457430 | CTGTCTGTCTGTCTG[-/TCTA]TCTATCTATCTATCT | 11059 |
rs768762858 | in-del | -/CAATAGGCCACCA | 1.64909e-05 | 0.00287144 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442767 | GTTTCATTGGTCGTT[-/CAATAGGCCACCA]TTATTGCCATGGTGA | 11059 |
rs768815186 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449539 | ATTTTTTTAAAATGT[-/A]AAAACTATTCTTAGC | 11059 |
rs768867275 | snp | C/G | 1.65121e-05 | 0.00287329 | intron-variant | WWP1 | GRCh38.p7 | 8:86461738 | AGAAAAAAGTTTAAA[C/G]GACCAGATAAACTTT | 11059 |
rs768869515 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427024 | AAAAATTAGCTGGGC[A/G]TGGTGGTCTGCGCCT | 11059 |
rs768939131 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356940 | TCTGATGTTGGCCAA[C/T]GACTTCGTCTAGTTT | 11059 |
rs768960593 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385598 | AGAAGTATATGTGGG[A/G]GCTCTCAAGGGTAAT | 11059 |
rs768978585 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416836 | CAAATCCAGCCCACC[A/C]CTTTTATAGGTACAG | 11059 |
rs768979408 | snp | G/T | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452643 | TGAAGTTGTTCCTCT[G/T]CAGTGGCTACAGTAC | 11059 |
rs768981472 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433176 | TTGATTTCCCTCTGC[A/G]TTTCTGTTCTTCTAT | 11059 |
rs768990169 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461520 | TCATATAGCTGAGGT[C/G]GCCATTGCTTTGCTC | 11059 |
rs769013900 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371362 | ATTTTATAAAATTCA[A/G]AATTACTCATTGAAG | 11059 |
rs769088234 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415600 | TGAATTTTGGCAAAT[A/G]CGTATGTCTGTGTAA | 11059 |
rs769103515 | snp | C/G/T | 4.96918e-05 | 0.00498436 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398371 | GAACAATTAAAACTT[C/G/T]CCTTGGAAAACAAGA | 11059 |
rs769122929 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376197 | TTTATTGTAACTTGC[A/G]TAGGACCAATGGACA | 11059 |
rs769124513 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363226 | AACAAAAAAAGCTGA[C/T]TGGTTAATGTCAGGT | 11059 |
rs769141519 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399520 | TATGACAAAGTGTGA[C/T]TTTTATTAATCTATA | 11059 |
rs769213572 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419370 | TTGCAGTGAGCTGAG[A/G]TCACACCACTGCAGT | 11059 |
rs769214384 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360814 | ATTACTAGGACAGAT[-/A]AAAATAGGGCAAGGT | 11059 |
rs769233680 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400976 | CTCTCCTGGTCACTT[-/A]ACATGATAATTTCCA | 11059 |
rs769291013 | in-del | -/TT | 1.65622e-05 | 0.00287764 | intron-variant | WWP1 | GRCh38.p7 | 8:86381478 | ACGTCTACTCCTGTA[-/TT]TTTGTTAATAATTTT | 11059 |
rs769304190 | snp | A/G | 1.69594e-05 | 0.00291194 | intron-variant | WWP1 | GRCh38.p7 | 8:86380898 | GGACGGAAAATCTTC[A/G]CAAGAAAGTGTATTT | 11059 |
rs769308369 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86453720 | CTGTTTCTTGTTTTG[A/G]TTTTTTGCTTGTTTT | 11059 |
rs769319485 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418280 | AACTTTGTGGAGCGT[A/G]TGGTCTAATATATAG | 11059 |
rs769354890 | snp | A/G | 1.77432e-05 | 0.00297847 | intron-variant | WWP1 | GRCh38.p7 | 8:86425173 | AGAGTCATTTTTAAG[A/G]TTGTCCTAGTGTGTT | 11059 |
rs769393848 | snp | A/G | 1.65509e-05 | 0.00287666 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448490 | TATTCTGGTGACTGA[A/G]GAGAACAAAGATGAA | 11059 |
rs769395445 | snp | C/T | 3.31664e-05 | 0.00407211 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411773 | CTCTAATTCTAGAAG[C/T]AGTTCTGCTTTTGAA | 11059 |
rs769398113 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437372 | TTATAGCTGAGTTCC[G/T]TTCCTACTGAGAAAT | 11059 |
rs769402941 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366401 | GTCTTTGATTAGGGA[A/G]ATCAGTGGTGATGAT | 11059 |
rs769475109 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428209 | CTTGCAGTATGCTAC[C/T]TATTCTGATTCTCTT | 11059 |
rs769479231 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402107 | TCGTATGTAGTTAAT[A/G]GAGACAACACACCTT | 11059 |
rs769502810 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458508 | CTTAAACTATAATAG[A/G]ATGGTCTCAGGAATC | 11059 |
rs769537066 | snp | A/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350963 | AAGTAAACAAACTAG[A/G/T]TTGTTCTTCTCTTTT | 11059 |
rs769546134 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358695 | CTATTTTTTTGTAGA[C/G]ACAAGGTTTTACCGT | 11059 |
rs769561730 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405469 | TAATGTATTTAATCA[C/T]GATGTGTGGCCCCTA | 11059 |
rs769578841 | snp | C/T | 4.99147e-05 | 0.00499549 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402193 | CGCATCTGAGCCTGC[C/T]GATGACACTGGTAAG | 11059 |
rs769594885 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352620 | TCCTCTCACCTTGCC[C/T]TCTCTCCCAATGTGC | 11059 |
rs769613177 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377349 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAGAGTGC | 11059 |
rs769615961 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393992 | CAAAGCCCTGTGGCG[A/G]GGCACTGAGGTCTCC | 11059 |
rs769628265 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412219 | TCCTTGGTGATCTGT[G/T]TTCCAGACCTCATAC | 11059 |
rs769666486 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396551 | AAGGTCTTCTTTTAT[A/C]ACATGGTTTAAACAT | 11059 |
rs769679659 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395275 | TTGAGCATAAAGGCC[A/G]CATATGGTTTCTGTT | 11059 |
rs769712215 | in-del | -/ATGTATG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422323 | GTACCAGTTTGTATT[-/ATGTATG]TATTTATTTATTTAT | 11059 |
rs769716034 | snp | A/G | 4.95233e-05 | 0.00497586 | intron-variant | WWP1 | GRCh38.p7 | 8:86431522 | GCCTTAAGTCGTCTT[A/G]CATATATCAGTAGGT | 11059 |
rs769716395 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449000 | CATTCCCAGCTAATT[G/T]AAAACAATTTTTTTT | 11059 |
rs769720026 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425642 | ATGGATAGTGATCTA[A/T]ACTATGTTATTTCAT | 11059 |
rs769739686 | snp | A/T | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425284 | CATAATACTCGAACT[A/T]CCACATGGGAGAGAC | 11059 |
rs769774228 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378294 | TTGAAATATTTCAAT[A/G]TTAAACTTTTCAAAT | 11059 |
rs769835999 | in-del | -/TATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387485 | ACATTCATATATGTA[-/TATT]TATTTATTTATTTAT | 11059 |
rs769890976 | snp | A/T | 3.31862e-05 | 0.00407333 | intron-variant | WWP1 | GRCh38.p7 | 8:86374022 | TAAATTCCCCTTTTT[A/T]AAAATAGGTTTTAGC | 11059 |
rs769910341 | snp | A/C | 0.00010489 | 0.00724112 | intron-variant | WWP1 | GRCh38.p7 | 8:86431368 | TTATATATAGATCCT[A/C]AATAGTTATTAAATA | 11059 |
rs769911500 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384109 | GTGTCTGCGTCCAAA[C/T]TTCCCCTTATCAGGA | 11059 |
rs769912397 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436606 | ATAGTGCCTTTGCAC[A/G]TAGAGGGTATTCAAT | 11059 |
rs769926182 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362999 | CTTAATAATTTAGCA[G/T]TTATATAGTACTCGA | 11059 |
rs769942103 | snp | C/T | 1.65589e-05 | 0.00287736 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466907 | GAATGTGGCTTCTTA[C/T]TTTGGAGGAGCTCTT | 11059 |
rs769997017 | snp | A/G | 1.90549e-05 | 0.0030866 | intron-variant | WWP1 | GRCh38.p7 | 8:86438686 | GAGGTAAAATAAAAA[A/G]CACATATCTGCCTTG | 11059 |
rs770020102 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | WWP1 | GRCh38.p7 | 8:86461217 | AGTACATTTAATTTC[A/G]TTACAGTTTGTGAAA | 11059 |
rs770031722 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348305 | CTCACTGCAGCTTCC[A/G]CCTCCTGGGTTCAAG | 11059 |
rs770047019 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86352039 | TAGCTAAAATATTCC[-/TT]TTTTTTTTTTTTTTT | 11059 |
rs770055948 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368953 | GGGTTGTCTCCTCAC[A/T]GACTATGAGCTCCTT | 11059 |
rs770059472 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437830 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 11059 |
rs770103456 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400344 | TCTCGGGGGGAAAAA[A/T]ATAAATAAATAAAGA | 11059 |
rs770112429 | in-del | -/GTGA | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342121 | TATCACCGGGCTGAT[-/GTGA]GTGAGGACTAGGTGG | 11059 |
rs770124471 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | WWP1 | GRCh38.p7 | 8:86431789 | TATTGCTTAGTGAGC[A/G]CATGAGATTTAGTCT | 11059 |
rs770138158 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447575 | CCACCTTGAAGGTAG[-/T]TTATTTTAATGATTG | 11059 |
rs770143254 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432673 | AGTGCAATGATGCGA[C/T]GTCAGCTCACTGCAA | 11059 |
rs770148262 | snp | A/G | 3.29772e-05 | 0.00406048 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435514 | AGCTTGCTCACTTCC[A/G]TTATTTGTGCCAGGT | 11059 |
rs770174441 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444254 | GTCAAGTATGGCAAC[A/G]ATATTTATGGCCAGC | 11059 |
rs770192111 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373552 | TGTTGAGACAGAGTC[C/T]CGCTCTGTTGCCCAG | 11059 |
rs770212850 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361523 | CTGGTATTCTTCATG[C/G]TATAGCTTCTTTCTG | 11059 |
rs770229787 | snp | C/T | 1.69269e-05 | 0.00290915 | intron-variant | WWP1 | GRCh38.p7 | 8:86457911 | GCCTGATTCTGTGCT[C/T]ATTTCCCAGGTTATG | 11059 |
rs770241960 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391179 | GAGATTGTTCCACTT[C/T]TTCACATTTAAGCCC | 11059 |
rs770245296 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374820 | GCTGAAGTGATCCTC[A/G]TGCTTCAGCCTCCCA | 11059 |
rs770278776 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391684 | TAAAAGGAGAATGAA[A/G]GAGTGGGGGTGGGGG | 11059 |
rs770295529 | snp | A/G | 1.65173e-05 | 0.00287374 | intron-variant | WWP1 | GRCh38.p7 | 8:86398506 | TTATATGTTTGTAAA[A/G]TTTCAAGGAAAAAGA | 11059 |
rs770341480 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86340738 | TAAGCACCTAGGGCC[C/T]GTGAAAGTCAGAATG | 11059 |
rs770399298 | snp | A/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427701 | GATCATAACACCAGA[A/T]CAACAACGTGGCAGC | 11059 |
rs770429800 | snp | C/G | 1.68227e-05 | 0.00290018 | intron-variant | WWP1 | GRCh38.p7 | 8:86448518 | GAATATATTGGGTAA[C/G]GTGATATACCTTATT | 11059 |
rs770487977 | snp | A/C/G | 4.95506e-05 | 0.00497727 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398392 | GAAAACAAGAATGGC[A/C/G]TAGCACAAACTGGTG | 11059 |
rs770505576 | snp | A/G | 3.30322e-05 | 0.00406387 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452592 | TTTTTCTCGAGGAGT[A/G]CAAGAACAGACCAAA | 11059 |
rs770560280 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455703 | ATTGTTAAAGTGTCA[A/G]TTCTCTCCAAATTGA | 11059 |
rs770658340 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408778 | AGCCGGGTGTGGTGA[C/T]GCATGCCTATAATCC | 11059 |
rs770663889 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378140 | GCATTTTAAAATACA[A/C]GTTTACTGTTCTTGA | 11059 |
rs770665928 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364772 | GATTATGCCACTGCA[C/G]TCTATCCTGGGCGAC | 11059 |
rs770692223 | in-del | -/AAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401918 | TAAAAAAGAAATAAC[-/AAAA]AAGAAACTTAAGAGA | 11059 |
rs770711742 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392419 | TGAGATGGCTGCCAT[C/T]CAAATACTGATAATT | 11059 |
rs770716764 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366203 | GGAGATTGTGGGAAG[A/T]ATAGGACCCATCAAG | 11059 |
rs770735913 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426909 | CATGCCTGTAATCCC[C/T]ACACTTTGGGAGGCC | 11059 |
rs770765709 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357675 | GACAAAAGTTTAATA[C/T]CAGGGATTCTGGATA | 11059 |
rs770778985 | in-del | -/CATGAATATTAAATACT | 5.71625e-05 | 0.00534584 | intron-variant | WWP1 | GRCh38.p7 | 8:86438686 | AGGTAAAATAAAAAA[-/CATGAATATTAAATACT]CACATATCTGCCTTG | 11059 |
rs770794234 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370860 | ATATTCATTCTTTTT[lengthTooLong]TTTTTTTTTTTTTTT | 11059 |
rs770812975 | snp | C/T | 1.65457e-05 | 0.00287621 | utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374037 | TAAAATAGGTTTTAG[C/T]TGAATTTTGGGACAT | 11059 |
rs770839042 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410934 | ATCTATTCACCCTTA[C/G]AGTTTTAATTTGACT | 11059 |
rs770842425 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant | WWP1 | GRCh38.p7 | 8:86431751 | TCATCTGTGTGAGTG[A/G]AAACCTGAAGTTCTC | 11059 |
rs770855712 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461441 | GTAGGTAGGGCTTCA[C/T]TTAGAAGAAAGAAAA | 11059 |
rs770863115 | snp | C/G | 3.30677e-05 | 0.00406605 | intron-variant | WWP1 | GRCh38.p7 | 8:86398548 | GTATATAAAAACCTA[C/G]TTTTTTTCTTTCTTG | 11059 |
rs770865889 | snp | C/T | 1.65985e-05 | 0.00288079 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411562 | AATCATCCTCATTTG[C/T]ACCAACTGATAATGC | 11059 |
rs770874605 | snp | C/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341342 | GAACCTTGAATATCA[C/T]GTTAATCTTTGTCAG | 11059 |
rs770874760 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358242 | GGTGAGGTGAGCATG[G/T]ACTTGAATCTTAGAT | 11059 |
rs770897083 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400196 | AATGAGCCAGGCATG[A/G]TGGTGCGCACCTGTA | 11059 |
rs770938405 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366743 | ATCCCAGTTTGGCCA[A/G]AACTGAGAGGTTTCC | 11059 |
rs770952224 | snp | A/T | 1.67773e-05 | 0.00289626 | intron-variant | WWP1 | GRCh38.p7 | 8:86430649 | ATTTCTACTTTCATA[A/T]TAAAACACTGTTATT | 11059 |
rs770960597 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461910 | TTGTTTTGTTTTTTT[-/A]AAAATATGTAAGATC | 11059 |
rs770973206 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360582 | GCTTTGCTCATAGGA[C/T]GCCATGCACACCTTT | 11059 |
rs771067511 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86398868 | AGTATACATTTTAGT[C/T]GTTTTTAATATATTA | 11059 |
rs771141330 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396740 | CTGGGAATACAGGCA[C/T]ATGCCACTGCACCTG | 11059 |
rs771151926 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361436 | TACCCTTACAACACT[A/G]TCAAAGGGGTTTTTC | 11059 |
rs771156436 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393498 | TCCACCCACCTCAGC[C/T]TCCCAAAGTGCTGGG | 11059 |
rs771216116 | in-del | -/TTGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370140 | ATACCACAAATATGA[-/TTGT]TTGATTTGAATTTCA | 11059 |
rs771259130 | snp | C/T | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411709 | AATGTATTCCTTCTA[C/T]CAGTGCAGAATTGGA | 11059 |
rs771266665 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390422 | TGAGCACTGAGTGAG[C/T]GAGACTCCGTCTGCA | 11059 |
rs771283804 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443668 | AGTAATCAATAGATA[C/T]ATTCTGAAGGAAAGA | 11059 |
rs771284237 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342487 | CGGAAGACCCGGAGG[A/G]GCGGAGTTTTCCTAA | 11059 |
rs771299212 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346875 | TTTGCTGGCATTAAG[A/G]ATTGTACTATACCTT | 11059 |
rs771325265 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419333 | TGAGGCAGAAGAATC[A/G]CTTGAACCTGGGAGA | 11059 |
rs771336859 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404831 | ACATTCCGCTATCTG[A/G]CTGTTGATTCTGTGC | 11059 |
rs771358021 | snp | A/G | 1.65151e-05 | 0.00287355 | intron-variant | WWP1 | GRCh38.p7 | 8:86435554 | GTAAATAAATCTTAT[A/G]CTCAATAATTTAGTC | 11059 |
rs771392823 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350777 | AAATCTGATTGACTG[A/G]GCTGGGTGGAAGCTG | 11059 |
rs771401121 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368548 | GAGCTTCCAAAGTTA[-/T]TTTTTCCAAAATGCA | 11059 |
rs771409401 | snp | A/G | 4.94588e-05 | 0.00497262 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461231 | CATTACAGTTTGTGA[A/G]AGAGACAGACAATGA | 11059 |
rs771418233 | in-del | -/T | 6.59875e-05 | 0.00574364 | intron-variant | WWP1 | GRCh38.p7 | 8:86431607 | GTGATTTTAACTTTA[-/T]CTTTTAGCTTACAGA | 11059 |
rs771428503 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437965 | CCACCACGCCTGGCT[A/C]ACTTTTTGTATTTTT | 11059 |
rs771452429 | snp | A/G | 4.957e-05 | 0.00497821 | intron-variant | WWP1 | GRCh38.p7 | 8:86461353 | GTAATTTCTCTGTAC[A/G]TAATTTTGTGATAAT | 11059 |
rs771479787 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440933 | CTTCATTTTCTTCTT[C/T]AGGCTCTGCTAGCTC | 11059 |
rs771507657 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428616 | TTTCAGAGGTTAAAT[A/G]GTAAGTTCTCATTTG | 11059 |
rs771513324 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant | WWP1 | GRCh38.p7 | 8:86398667 | TTTGAATATGGGTGG[C/T]GACATGATGTGGAAC | 11059 |
rs771537843 | in-del | -/TTAT | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344557 | CTATACACAAATGCC[-/TTAT]TTGTCTTTTAATATA | 11059 |
rs771555722 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360244 | ATAAGTTTCTGGTGG[-/T]TTTTTTTTGCTTGGT | 11059 |
rs771562484 | snp | A/T | 4.96151e-05 | 0.00498047 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411571 | CATTTGCACCAACTG[A/T]TAATGCGTCTGTCAC | 11059 |
rs771588506 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376250 | AAATGATCTTGACCT[A/G]TGTATAAGAGTTCTT | 11059 |
rs771610672 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461086 | AATGCTGGGATTACA[-/G]GTGTGAGCCACCACG | 11059 |
rs771617012 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429505 | TCATTATTATAGAAT[G/T]CTTGATAGAATACTT | 11059 |
rs771666966 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RMDN1, WWP1 | GRCh38.p7 | 8:86468642 | GCAGCTTTCCAGTTC[A/G]TTTTCAGGGTGCTGG | 11059 |
rs771680583 | snp | C/T | 1.65086e-05 | 0.00287298 | intron-variant | WWP1 | GRCh38.p7 | 8:86431564 | ACCTTGAATGAGATA[C/T]TTTTAGTACCTAGAA | 11059 |
rs771796936 | snp | A/T | 2.02542e-05 | 0.00318225 | intron-variant | WWP1 | GRCh38.p7 | 8:86448128 | AAATTTTAAATAAAA[A/T]TTTTCATTTTTCTTT | 11059 |
rs771814392 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393693 | ACTTACAAGCTATGT[A/T]ACCTAATGTGTTCAT | 11059 |
rs771835365 | snp | C/T | 1.6473e-05 | 0.00286988 | stop-gained, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427737 | ACCATGGAATCTGTC[C/T]GAAATTTTGAACAGT | 11059 |
rs771837137 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355965 | TTCAAATTCAGACTT[-/A]ACTAGTTTCATGGCC | 11059 |
rs771842957 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458536 | ATCCAAGTGTACCAC[A/C]CTAATCTTGAACATT | 11059 |
rs771879285 | snp | C/T | 3.38329e-05 | 0.00411282 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448272 | TTTATAACTCCCTTA[C/T]CTGGATAAGGTTTGA | 11059 |
rs771915171 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367762 | TCTGTCTTCTCATAT[C/T]CTGGGGACCAAGGAC | 11059 |
rs771946094 | snp | A/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411653 | TACTACTGTTGAAGA[A/T]CCTCCAGTTCAAGAA | 11059 |
rs771954158 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368800 | CGCAGTTCTCTCAGA[A/G]GTTATCTTCTCTGTG | 11059 |
rs771974145 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384635 | TTAGTACTTGGACTC[-/T]TGAGTTTTAGTTGGC | 11059 |
rs772007298 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369642 | TTGCCTTTATTCTCA[A/G]TAGTTATCTTTCTGT | 11059 |
rs772015985 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427078 | TGAGGCAGGAAAATC[A/C]CTTGAACCTGGGAGG | 11059 |
rs772088674 | in-del | -/AAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438137 | AAGTAAGCTAGAGAA[-/AAG]AAAATTTTTTTAGAA | 11059 |
rs772098692 | in-del | -/CATA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430798 | AGATATATATCTCTC[-/CATA]TATATATATATATAT | 11059 |
rs772101198 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402093 | AAAACTCATGCTGCT[C/T]GTATGTAGTTAATGG | 11059 |
rs772123139 | snp | A/G/T | 6.98501e-05 | 0.00590941 | intron-variant | WWP1 | GRCh38.p7 | 8:86380696 | ACTTTTTGGCAACAC[A/G/T]TACTCACTAGTGAAT | 11059 |
rs772145569 | in-del | -/TGT | 3.44116e-05 | 0.00414784 | intron-variant | WWP1 | GRCh38.p7 | 8:86401969 | AAAATTCTCATGAAA[-/TGT]TGTTGAATTATACTT | 11059 |
rs772156308 | snp | A/G | 1.65479e-05 | 0.0028764 | intron-variant | WWP1 | GRCh38.p7 | 8:86398673 | TATGGGTGGCGACAT[A/G]ATGTGGAACATATTT | 11059 |
rs772212633 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428401 | AAACAAAACTCCTCT[A/G]ATAAATGGTGTGATC | 11059 |
rs772243625 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442417 | GATCAGTGAATTTGT[A/G]GTTTGGCCACATCGA | 11059 |
rs772251921 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371000 | CCTCCTGAGTAGCTG[G/T]GATTACAGGCACCTG | 11059 |
rs772255304 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387743 | TAGCCAGACTGGTCT[C/T]GAACTCCTGACCTCA | 11059 |
rs772267841 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412573 | AGTATATATGGACAC[A/G]TGCTTTCCAACACAG | 11059 |
rs772344112 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463664 | TAATTAAATGTGTCA[A/G]CATTTAGAAAATCCT | 11059 |
rs772352355 | snp | C/T | 1.66815e-05 | 0.00288799 | intron-variant | WWP1 | GRCh38.p7 | 8:86430673 | TGTTATTTTATTTCT[C/T]TCCCTAATCTTTTCT | 11059 |
rs772393771 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358822 | CCCATTTATTATTTA[A/G]TAGGGGCCAGACATT | 11059 |
rs772415930 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402816 | AAAATATATTTCTGA[A/G]AGAACTTTAGTTAAT | 11059 |
rs772417575 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436269 | AATACTTGGCTAAGA[A/G]TTTATTACCTCAAAG | 11059 |
rs772429373 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467808 | AAAATTTTGGTTTTT[A/T]TGAAGCCAGATGGAT | 11059 |
rs772444234 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385490 | GATTTCTGGCAAGAC[A/G]TTTTTTTAAAAAAAG | 11059 |
rs772448232 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443126 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC | 11059 |
rs772474004 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418036 | GGCTAGAGAGCAGCT[A/G]TATAAATTATTATTT | 11059 |
rs772476881 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350645 | TGATGGCTGTCCTCC[C/T]TACCCTAAATTATTT | 11059 |
rs772492166 | snp | A/G | 1.6615e-05 | 0.00288223 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411789 | AGTTCTGCTTTTGAA[A/G]CAGCCAAATCAAGAC | 11059 |
rs772508040 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464923 | CACATGCGCGCGCGT[-/GT]GTGTGTGTATTGAGA | 11059 |
rs772527631 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433565 | AAAAAAAAAAAATTA[C/T]AACAACAACAACAAA | 11059 |
rs772534932 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400804 | TGAGCTTGGAGAGAA[A/G]TAGGTTAGAGAGAAG | 11059 |
rs772557224 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364346 | AAATGGTTAAAATTG[C/G]CATTAAAAAGGGAAT | 11059 |
rs772563887 | in-del | -/ATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383268 | CAGTACCTTGCCTGG[-/ATT]ATTATTATTTAACCA | 11059 |
rs772565204 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455603 | ATTTAACCAAAAACA[C/T]ACAAGACCTCTATAC | 11059 |
rs772569394 | snp | A/G | 1.69735e-05 | 0.00291315 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438623 | CTTGAGGAGGCGCTT[A/G]TATGTAATATTTAGA | 11059 |
rs772584047 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384244 | TAAAACTTCAACATA[C/G]GAATTTGGTGGGGGA | 11059 |
rs772630419 | in-del | -/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414249 | GTGTGTGTGTGTGTA[-/TA]TGTGTGTGTATGTAA | 11059 |
rs772664526 | snp | G/T | 6.62844e-05 | 0.00575655 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448493 | TCTGGTGACTGAGGA[G/T]AACAAAGATGAATAT | 11059 |
rs772765444 | snp | A/G | 6.59685e-05 | 0.00574281 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461816 | TTGAAAAAGTTGGCA[A/G]AGACACTTGGTTACC | 11059 |
rs772767671 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457091 | TCTGTTGAAAATCTT[C/T]GAACTATATACCTAA | 11059 |
rs772780744 | snp | A/G | 3.40119e-05 | 0.00412368 | intron-variant | WWP1 | GRCh38.p7 | 8:86380901 | CGGAAAATCTTCACA[A/G]GAAAGTGTATTTTTT | 11059 |
rs772816997 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341269 | GATGAGTGGGCACAT[A/G]TGGGGCACTGTGAAG | 11059 |
rs772833158 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346602 | AGTGCGATTGGTAAA[-/C]AGTTGACTTTTCTGC | 11059 |
rs772835948 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415797 | ATGTAACCTTTATTA[A/T]TTTTCTAGCACTTAA | 11059 |
rs772855966 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363350 | TCTGCTTTAACTGTC[C/T]GCTTCCTTGAACTTT | 11059 |
rs772873691 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376256 | TCTTGACCTATGTAT[A/G]AGAGTTCTTAGGTAA | 11059 |
rs772875045 | in-del | -/AGTTGG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451574 | ACAAATGGGAAGAAA[-/AGTTGG]AGTTGGAGTTGGAGT | 11059 |
rs772893498 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422664 | AGGTGTGAGCCACCA[C/T]GCCCGGCCCACCAGT | 11059 |
rs772894725 | snp | A/G | 6.71998e-05 | 0.00579615 | intron-variant | WWP1 | GRCh38.p7 | 8:86448350 | ATTTTGTTAATTAGT[A/G]TATATATATTTATTT | 11059 |
rs772919888 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441422 | GTGTTTTATAACCTT[G/T]AGAAAAACGTTTATT | 11059 |
rs772940315 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371189 | GGCATGAGCCACCGC[C/T]CCTACCTGTAGTTCA | 11059 |
rs772971796 | snp | A/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367845 | ATAAGCACAGTATTA[A/T]TACGGCTCAGCAGAA | 11059 |
rs772978514 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377351 | GATCCGCCTGCCTCG[A/G]CCTCCCAGAGTGCTG | 11059 |
rs772997689 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369539 | CATGTAGTAAAGTGA[A/G]TAGTTTTTTACCTGA | 11059 |
rs773033800 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86454170 | AGTATATAATAGGAT[A/T]GTATTTGCATATAAC | 11059 |
rs773045444 | snp | A/G | 3.3129e-05 | 0.00406982 | intron-variant | WWP1 | GRCh38.p7 | 8:86461880 | AATACGAAGGTGAAA[A/G]CCACAGAGAATCTTT | 11059 |
rs773065668 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355303 | CTCATCAGCAGTTCT[C/G]GGTTTGGCCTGCCAT | 11059 |
rs773069639 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407291 | CAATCTTTCTTATAT[A/C]CATTTGTCAACAGAT | 11059 |
rs773085476 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408766 | GCAAAAAAATTTAGC[C/T]GGGTGTGGTGACGCA | 11059 |
rs773122499 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345535 | CTGCCTCAGTCTCCC[A/G]AATAGCTTGAACTAC | 11059 |
rs773157993 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394423 | AAGCACCTACCTTCT[C/G]TCAGTTGCTGAGGAT | 11059 |
rs773173491 | in-del | -/CATATATATATATA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430798 | AGATATATATCTCTC[-/CATATATATATATA]TATATATATATATAT | 11059 |
rs773195155 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459184 | GGGATTACGGGTGTG[C/T]GCCACCATGCCCGGC | 11059 |
rs773240325 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402108 | CGTATGTAGTTAATG[C/G]AGACAACACACCTTC | 11059 |
rs773276258 | in-del | -/TAAC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459363 | TTTAAAAATGCAAAT[-/TAAC]AAAAATGTTGGAGAA | 11059 |
rs773276850 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389743 | CGGCCGGGCAGAGGC[A/G]CCCCCCCACCCACCT | 11059 |
rs773278067 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449198 | ATGTAGGCATTTTTC[C/T]AAGATTTTATTTCAA | 11059 |
rs773285554 | snp | A/G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463602 | TGAGCCACCATGCCC[A/G/T]GCCAATTAGTGGTAT | 11059 |
rs773291753 | snp | A/G | 3.15075e-05 | 0.00396897 | intron-variant | WWP1 | GRCh38.p7 | 8:86431373 | TATAGATCCTAAATA[A/G]TTATTAAATATTATA | 11059 |
rs773301386 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411299 | TAAGGTTGTTATTAT[G/T]ATACATACTTAAATT | 11059 |
rs773308597 | snp | C/T | 1.94937e-05 | 0.00312194 | intron-variant | WWP1 | GRCh38.p7 | 8:86438689 | GTAAAATAAAAAACA[C/T]ATATCTGCCTTGAAA | 11059 |
rs773323562 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371502 | TTTTTGCCATTATTT[A/G]GCACTATCAACATTC | 11059 |
rs773330160 | snp | C/T | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461822 | AAGTTGGCAAAGACA[C/T]TTGGTTACCAAGAAG | 11059 |
rs773331204 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436760 | TTTTCATAATGAGAC[A/G]TCTTATTCCCCCCCT | 11059 |
rs773336050 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462773 | AAATTTCTGCTTGTG[G/T]TGCAAAAGCAATGGT | 11059 |
rs773370868 | snp | A/G | 1.67685e-05 | 0.00289551 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442659 | GAAGTTTTGAACCCA[A/G]TGTATTGCTTATTTG | 11059 |
rs773372021 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395531 | TGGTGACCAGGTCAC[C/T]AGGTGACTAGGTCAG | 11059 |
rs773380843 | snp | A/C | 4.97574e-05 | 0.00498761 | intron-variant | WWP1 | GRCh38.p7 | 8:86425326 | CCTCCAGGGTAATAT[A/C]GCACTCTTTATGCAT | 11059 |
rs773396260 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455679 | AAATGAAGAGATATA[C/T]GATGTTATATTGTTA | 11059 |
rs773424150 | snp | A/G | 1.65658e-05 | 0.00287795 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466912 | TGGCTTCTTATTTTG[A/G]AGGAGCTCTTGCATT | 11059 |
rs773425058 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364499 | GTACTGTAAAGCAGA[A/G]GAGTTTTCTGTGTAA | 11059 |
rs773437846 | in-del | -/AG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392773 | TATCAACACAAACTC[-/AG]AGATATTTTGAAGTC | 11059 |
rs773451526 | in-del | -/G | 1.64972e-05 | 0.00287199 | intron-variant | WWP1 | GRCh38.p7 | 8:86452713 | GCTATTGTAGGGAAT[-/G]TTAGTGGGGGGAGGG | 11059 |
rs773457346 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358978 | AGATGACACCTGAGC[A/G]GACAGATGATTAGAA | 11059 |
rs773509607 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450456 | TTAAGCCTGAGCCTT[C/T]CACAAAGTCCAACAA | 11059 |
rs773523095 | snp | C/T | 1.65345e-05 | 0.00287524 | intron-variant | WWP1 | GRCh38.p7 | 8:86398544 | AGAAGTATATAAAAA[C/T]CTAGTTTTTTTCTTT | 11059 |
rs773560096 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448791 | ACTCAGTGTTTTCTT[-/G]AATTCCATGATCCTA | 11059 |
rs773569074 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402957 | TGAATAGCTCTCAGA[A/G]AGTTTATTTTCCAAA | 11059 |
rs773599307 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364401 | CTTCATACTCAAAAC[-/TG]TGATATGTATGGTGC | 11059 |
rs773617258 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357661 | AAAGCTGTTTTGATG[-/A]CAAAAGTTTAATATC | 11059 |
rs773638917 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410278 | TCATAGAATTTTCTC[-/A]AAAACCTTTCTGAGC | 11059 |
rs773660074 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370113 | AACTTGTTTCCATCT[C/T]TTCTTTTTAAAATAC | 11059 |
rs773694927 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389416 | ATCTTGCACCCCCCT[G/T]AATCCATTTAACCCT | 11059 |
rs773726812 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419526 | AATACTCAAAGGACT[-/A]AAAAAACTCTTGGAA | 11059 |
rs773786638 | in-del | -/TATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422332 | TTGTATTTATTTATT[-/TATT]TATTTATTTATTTAT | 11059 |
rs773827652 | snp | A/G | 3.30289e-05 | 0.00406366 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452594 | TTTCTCGAGGAGTAC[A/G]AGAACAGACCAAAGC | 11059 |
rs773850604 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460053 | TTCCACTCTTAATCT[A/G]CTCCCTATGTTCCTT | 11059 |
rs773902784 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427258 | TTAGAAATTATATTA[A/G]GGCTAATGCTTTCCC | 11059 |
rs773909515 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456516 | GGGAAATGCAAATCA[-/T]AAGCACCACTTTGAG | 11059 |
rs773976350 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354962 | AAAAAACCCTCACAA[-/T]TACTATATTAATTTG | 11059 |
rs774003211 | snp | A/C | 7.44144e-05 | 0.00609932 | intron-variant | WWP1 | GRCh38.p7 | 8:86431392 | TTAAATATTATACTC[A/C]CTTTATATTTCAGAA | 11059 |
rs774021897 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348789 | ACACAAGGAACCAGG[G/T]GAGTGTTGTTTCAGT | 11059 |
rs774042882 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433329 | AATGACTCACAAATT[G/T]AGCTCAGACTTCTCA | 11059 |
rs774056120 | snp | A/G | 1.68371e-05 | 0.00290143 | intron-variant | WWP1 | GRCh38.p7 | 8:86448519 | AATATATTGGGTAAG[A/G]TGATATACCTTATTA | 11059 |
rs774103986 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378490 | GGTGACTCATTTTCT[C/G]ATAGTTTAAAAATAC | 11059 |
rs774105908 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465544 | GGTGGGAGGAGGGAG[G/T]ATTGCTTCAGCCTGG | 11059 |
rs774121684 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375050 | ATGACATTATCATAA[C/T]ATCTGTTTTTATCCT | 11059 |
rs774170810 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396675 | CATCACTTGCTGCAG[C/T]CTCGAACTCCTGGGC | 11059 |
rs774178193 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348507 | CAGGCATGAGCCACC[-/A]ACGCCTGGCCGTCTT | 11059 |
rs774185332 | snp | C/T | 1.66905e-05 | 0.00288876 | intron-variant | WWP1 | GRCh38.p7 | 8:86461896 | CCACAGAGAATCTTT[C/T]GTTTTGTTTTTTTAA | 11059 |
rs774196333 | snp | A/G | 1.6534e-05 | 0.00287519 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442682 | CTTATTTGAGTATGC[A/G]GGCAAGAACAACTAT | 11059 |
rs774230655 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441606 | GCCTTCTCATGTGGC[A/G]TCAGTGGGCTGAATC | 11059 |
rs774276760 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445388 | CTATTTTTCCCATCT[A/G]TTTATGTCCATGTGT | 11059 |
rs774280576 | in-del | -/AG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452476 | TTTAGAAAAAGAGAA[-/AG]AACTATAGAAGTTCT | 11059 |
rs774296259 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460415 | AAGGACAAATCATTT[-/A]AAACTCTCTAGGCCT | 11059 |
rs774323203 | snp | A/C | 0.00257598 | 0.035796 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466933 | CTCTTGCATTTAAAT[A/C]CCCCAGCCAAGAAAA | 11059 |
rs774328157 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414513 | GCATACACAGCACCA[C/G]GCTGTGTAACCCTTT | 11059 |
rs774352511 | in-del | -/TTG | 3.3042e-05 | 0.00406447 | intron-variant | WWP1 | GRCh38.p7 | 8:86398561 | TAGTTTTTTTCTTTC[-/TTG]TTGTTCAGTAGAAAT | 11059 |
rs774368754 | snp | A/G | 4.96635e-05 | 0.0049829 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411567 | TCCTCATTTGCACCA[A/G]CTGATAATGCGTCTG | 11059 |
rs774391966 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398415 | AACTGGTGAATTGAC[A/G]GTTGTGCTTGATGGA | 11059 |
rs774413062 | in-del | -/CT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420751 | TCACAGACTGTATGA[-/CT]CTGTTTATGTGAAGG | 11059 |
rs774414377 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363907 | ACTAAAATGACAAAA[A/G]TAGTGTACGTGAAAC | 11059 |
rs774414394 | snp | A/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461813 | GCATTGAAAAAGTTG[A/G]CAAAGACACTTGGTT | 11059 |
rs774419798 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419535 | AAGGACTAAAAAACT[C/G]TTGGAAATTTAATTC | 11059 |
rs774423426 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425693 | TTAAATGACTTAAAG[G/T]CCCAAATGATTTAAT | 11059 |
rs774426722 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427046 | TCTGCGCCTGTAATC[C/T]CAGCTACCCAGGAGG | 11059 |
rs774469003 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421759 | AACCCGGGAGGCGGA[A/G]CTTACATGAGCCAAG | 11059 |
rs774469907 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447889 | GGAAGATTGAGGCAG[G/T]GTATGGTAATAGAAG | 11059 |
rs774494839 | snp | G/T | | | intron-variant, nc-transcript-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86343103 | TACCTTCTCCAGCCC[G/T]GGAGTCGGGAGTTTT | 11059 |
rs774514461 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427734 | CCTACCATGGAATCT[G/T]TCCGAAATTTTGAAC | 11059 |
rs774532803 | in-del | -/G | 1.64909e-05 | 0.00287144 | frameshift-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86442769 | TTCATTGGTCGTTTT[-/G]ATTGCCATGGTGAGT | 11059 |
rs774543446 | snp | C/T | 9.91686e-05 | 0.00704092 | intron-variant | WWP1 | GRCh38.p7 | 8:86398554 | AAAAACCTAGTTTTT[C/T]TCTTTCTTGTTGTTC | 11059 |
rs774558404 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376211 | CGTAGGACCAATGGA[C/T]AGTACACCTGAGGTG | 11059 |
rs774613912 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411710 | ATGTATTCCTTCTAC[C/T]AGTGCAGAATTGGAA | 11059 |
rs774628305 | snp | C/T | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86457927 | ATTTCCCAGGTTATG[C/T]TGTGTGGCATGCAGG | 11059 |
rs774657730 | in-del | -/ATATATATATAT | 0.0294807 | 0.117776 | intron-variant | WWP1 | GRCh38.p7 | 8:86430799 | GATATATATCTCTCC[-/ATATATATATAT]ATATATATATATATA | 11059 |
rs774662373 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462633 | GCAAGGGTGAATGCA[C/G]GGAGAGTAGTTAGAA | 11059 |
rs774682145 | snp | A/T | 1.66765e-05 | 0.00288756 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380766 | AAAGAACTGGTTCGG[A/T]ACAGCAATATATACA | 11059 |
rs774682618 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414229 | AAGTTTGTTTTTCTG[-/TG]TGTGTGTGTGTGTGT | 11059 |
rs774690098 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391902 | GCCCTTGAGAAAGAC[A/G]CTCACATGTTATAGG | 11059 |
rs774790902 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416879 | GTCACTGTGAGTCAT[G/T]GAGACAAAGCCAGAG | 11059 |
rs774795559 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400638 | GAAATTCTTCTAACT[C/T]TAGAGAATAATATTT | 11059 |
rs774838477 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366514 | TTCCCTTCTCCTGAC[A/G]TGTAGTTCCAGTGAT | 11059 |
rs774859127 | snp | A/T | 3.30028e-05 | 0.00406205 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374088 | CTGATACTAGTAATA[A/T]CCACAGTGGAAGGTT | 11059 |
rs774912106 | snp | A/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411573 | TTTGCACCAACTGAT[A/G]ATGCGTCTGTCACGG | 11059 |
rs774916277 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445624 | TGGGGAACATACAGT[A/G]CTTGTGTCCTTTGGT | 11059 |
rs774922871 | in-del | -/CTTAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355701 | TTATACTTTTACACA[-/CTTAT]CTTTTTACGATTAAT | 11059 |
rs774946271 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440130 | TCAGACATAAGAAAG[A/G]TACATCTTAGAAATG | 11059 |
rs775055599 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86382480 | AGGGTGGGCAGATCA[C/G]TTGAGATCAGAAGTT | 11059 |
rs775086989 | snp | A/C | 1.65397e-05 | 0.00287569 | intron-variant | WWP1 | GRCh38.p7 | 8:86431767 | AAACCTGAAGTTCTC[A/C]TTTAAATATTGCTTA | 11059 |
rs775092451 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421125 | TTTTATATAAACAAA[-/T]AAAGTAAATCATAAC | 11059 |
rs775093173 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443150 | TGATCTCAGCTAACT[A/G]CAACCTCCACCTTGC | 11059 |
rs775097803 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367533 | TGTCGTTTATTATCT[A/G]CATTCAGGACTTTTT | 11059 |
rs775134934 | snp | A/G | 1.65941e-05 | 0.00288041 | intron-variant | WWP1 | GRCh38.p7 | 8:86430692 | CTAATCTTTTCTCCA[A/G]TCAGGCTTCAATGTT | 11059 |
rs775137795 | snp | A/C | 1.65026e-05 | 0.00287246 | intron-variant | WWP1 | GRCh38.p7 | 8:86431595 | AAGGTTCATCTTGTG[A/C]TTTTAACTTTATCTT | 11059 |
rs775138801 | snp | G/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341378 | CTCCGAAAAGCCAAA[G/T]AATGATTTTAAGCAG | 11059 |
rs775139995 | snp | A/G | 3.30628e-05 | 0.00406575 | intron-variant | WWP1 | GRCh38.p7 | 8:86457884 | TATTCTCTTCACTAA[A/G]TCTTTATTGTGGCCT | 11059 |
rs775198805 | snp | A/G | 1.66189e-05 | 0.00288256 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466939 | CATTTAAATACCCCA[A/G]CCAAGAAAAATTGCA | 11059 |
rs775212575 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421107 | CCTTCTTTCCCGTGA[A/G]CTTTTTATATAAACA | 11059 |
rs775228665 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86397061 | GGTGATTAGTAGTTC[C/T]AGATTTTTGTCTTGT | 11059 |
rs775232590 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428793 | TATAGTAATTATACC[A/G]TGTGGTATATATAGT | 11059 |
rs775254736 | snp | A/C | 1.64928e-05 | 0.00287161 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398584 | CAGTAGAAATACAGG[A/C]AAATGGTGATGCCTT | 11059 |
rs775269836 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388998 | TCTTCCAAGAAGTTG[A/C]ATATTTTACCTCTGA | 11059 |
rs775294508 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418828 | GTAAATTTTCAAATA[C/T]ACACCCAACACAGAT | 11059 |
rs775338765 | in-del | -/GTGT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464921 | CACACATGCGCGCGC[-/GTGT]GTGTGTGTATTGAGA | 11059 |
rs775356122 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378465 | AGTTAACTCTCCCTA[C/T]CCTCTCACAGGTGAC | 11059 |
rs775385910 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468452 | AAAAAAATTCTAATG[C/T]ATGTGACAGGTTATG | 11059 |
rs775398609 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343673 | CTGCTGTGGTAAATA[C/T]ATGAAACCTTCATTA | 11059 |
rs775479912 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439136 | ATCATGATATCAGGA[G/T]ATCGAGACCATCCTG | 11059 |
rs775489225 | in-del | -/TAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384284 | GCCCCAAACAAAAGG[-/TAAA]TAAATTTATTTGAAG | 11059 |
rs775491616 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86390478 | CTGGCAGATCACTCG[C/T]GGTCAGGAGCTGGAG | 11059 |
rs775572725 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440020 | ATATTTCCTCATTTA[C/T]AACATCATTAAACTT | 11059 |
rs775578474 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86441231 | ACACTCTCACAAGAC[C/T]TGCTCCATCCTCTTA | 11059 |
rs775601573 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438339 | CCTGTGCATTCACCA[A/T]GTTGACTTAAACTCA | 11059 |
rs775622339 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418323 | TCTTTTGAATGGTTT[A/G]TAGCGTTTCCTTGTG | 11059 |
rs775640477 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368980 | CCTTGAAAGAGGGAA[G/T]CGTGTCTTACTCATC | 11059 |
rs775665283 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399362 | TGGCATTCACAGTTC[A/G]TGACAATTAATAGAG | 11059 |
rs775669291 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380717 | ACTAGTGAATTATTT[C/G]TCTGTTAGTTTCTAG | 11059 |
rs775673934 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421853 | TTTTTGAAAATATAA[A/G]TTTACCATATTAACA | 11059 |
rs775675643 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86345001 | TTCAGAAGGATTAGT[A/G]GGATAGAGGTCTGTA | 11059 |
rs775685299 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391192 | TTCTTCACATTTAAG[C/T]CCTAGTGAGCTTTCA | 11059 |
rs775712444 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346719 | CTGTTGTTTTTTACT[C/G]TTTGTATAAAAATAT | 11059 |
rs775741335 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425392 | ATTTATTTAGTACAG[C/T]GTAATTTGATTCTTT | 11059 |
rs775769270 | snp | C/T | 5.21789e-05 | 0.00510752 | intron-variant | WWP1 | GRCh38.p7 | 8:86380913 | ACAAGAAAGTGTATT[C/T]TTTGGAATATGTTTT | 11059 |
rs775777416 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463929 | AGCCGGGTGTGGTGG[C/T]ACACACCTGTAGTCC | 11059 |
rs775781665 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | WWP1 | GRCh38.p7 | 8:86435587 | CTCTTTATACAATAC[A/G]TATACTATAACTCAG | 11059 |
rs775788415 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385552 | AAAGTCCTTGAAGGC[-/A]GATTACAATATGGAG | 11059 |
rs775852669 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413945 | CTGTTTTATAAATGA[A/G]GGAAGCCGGCATTCC | 11059 |
rs775853681 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86374880 | TTGCCTGGCTAATTT[A/T]AAAAAAAATTTTTTT | 11059 |
rs775888094 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460458 | ATGTACAGTGGGGAT[G/T]CTAATGATTCTACCT | 11059 |
rs775905244 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361539 | TATAGCTTCTTTCTG[A/C]CTTAATAGTTTTGTC | 11059 |
rs775918978 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384142 | CCAGTCATTGGATTA[A/G]GGCCTACCCCAATGA | 11059 |
rs775961303 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417226 | ACATGCCCACAACCC[A/G]GGATGCCCCAGCACA | 11059 |
rs775975643 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422322 | AGTACCAGTTTGTAT[-/G]TTATTTATTTATTTA | 11059 |
rs776034384 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465352 | TAGACCCAAAGAATT[A/C]TCTGATGGTCCAGGT | 11059 |
rs776035317 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429567 | AAGAATGGAGGCATA[C/G]ATAAAAATGTGTTTT | 11059 |
rs776040960 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419049 | TTTTCAGTGCCCTTC[C/T]CATTAGATATCTGAG | 11059 |
rs776053128 | snp | C/G | 1.69364e-05 | 0.00290997 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380732 | GTCTGTTAGTTTCTA[C/G]TGCCAAACTTAAAAG | 11059 |
rs776087283 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452532 | ACATATAAATTACCT[A/G]TTTTTAAATACCATC | 11059 |
rs776103142 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86448732 | CATTTTCCCTTTTTT[A/T]ACTTAGGCTTTTAAA | 11059 |
rs776155938 | snp | C/T | 0.000151221 | 0.00869412 | intron-variant | WWP1 | GRCh38.p7 | 8:86435748 | CCATTTGTCTCATTG[C/T]ATTCTGTGCATCTAA | 11059 |
rs776158254 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450545 | AAAACAGTCTAAATA[A/G]AATTTCACTATGTAA | 11059 |
rs776185929 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468146 | TCCATTTGTATCATG[C/G]TTTTAATATGCACTG | 11059 |
rs776194607 | in-del | -/AAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466169 | CTTTGTAAACTGAAA[-/AAT]AATAGTTATTTTAAG | 11059 |
rs776221214 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425436 | TTCAATTTCTTTACA[C/T]TTCCTTATATAAATA | 11059 |
rs776225114 | snp | A/G | 4.94425e-05 | 0.0049718 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411684 | ATACTGACTTCCTCA[A/G]AAAACAATGAATGTA | 11059 |
rs776275901 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant, splice-donor-variant | WWP1 | GRCh38.p7 | 8:86435540 | CAGGTACTATAGTGG[C/T]AAATAAATCTTATAC | 11059 |
rs776276535 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402096 | ACTCATGCTGCTCGT[A/G]TGTAGTTAATGGAGA | 11059 |
rs776277994 | snp | A/G | 3.30169e-05 | 0.00406293 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411578 | ACCAACTGATAATGC[A/G]TCTGTCACGGGTACT | 11059 |
rs776279442 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349687 | TCTCCTTGGTTAGAA[A/G]AGAGGAGAACATTTG | 11059 |
rs776303417 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364898 | AGAGAGAAAATAAAG[G/T]AAAATTAAAAATTAA | 11059 |
rs776308925 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86403126 | TAAACATCTTAGGAC[A/G]TGTTTAAGATTATTA | 11059 |
rs776318473 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86455895 | AGTAAATAAGATAGC[A/G]TGGTATTTGTGAAAG | 11059 |
rs776320522 | snp | A/C | 1.65198e-05 | 0.00287395 | utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86374050 | AGCTGAATTTTGGGA[A/C]ATGGCCACTGCTTCA | 11059 |
rs776329579 | snp | A/C | 0.33656 | 0.234537 | intron-variant | WWP1 | GRCh38.p7 | 8:86430803 | TATATCTCTCCATAT[A/C]TATATATATATATAT | 11059 |
rs776351565 | snp | A/G | 1.74946e-05 | 0.00295753 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448150 | TTTTTCTTTGCAGGC[A/G]CTATTTCATGGAAAG | 11059 |
rs776355661 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366327 | GCTTGGGGTATGATG[C/G]CATGGGGATGATGGG | 11059 |
rs776417397 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392221 | CCAAGATTGAGGCCT[A/C]GTCAAGAAGGTCCTG | 11059 |
rs776426327 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86411036 | TGGATTGCAGTACTG[C/G]GTTATTTCTTGAAAA | 11059 |
rs776450371 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408817 | TGGGAGGCTGGGGCA[A/G]GAGAATTGCTTGAAC | 11059 |
rs776464497 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369807 | TGAAAGCTGTATCTG[G/T]CCTTCTTTTGCATCA | 11059 |
rs776480662 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434585 | TTTAACAATGCCTTT[G/T]TTATTGTTTTATTGT | 11059 |
rs776485683 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392538 | TTAAGTTCAATTCGA[A/G]GTAAATTATGTCCAA | 11059 |
rs776510356 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86446100 | AATTCTCTTGCCTCA[A/G]CCTCCTGAGTAGCTG | 11059 |
rs776512149 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461481 | TAATATCAAAGCACT[C/T]GTAAGACAAAAATGA | 11059 |
rs776518299 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464878 | GAAGACCTCTGCCTT[A/C]AATAAAAGTGATAGA | 11059 |
rs776539182 | snp | A/G | 0.000203455 | 0.010084 | intron-variant | WWP1 | GRCh38.p7 | 8:86402002 | AAATGATTGAAATAA[A/G]GCATTTTTTTTTCAA | 11059 |
rs776544937 | in-del | -/CTCTCC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391101 | AATAAACCCCCCAGA[-/CTCTCC]TAACATAAATTATTT | 11059 |
rs776594160 | snp | A/G | 1.65466e-05 | 0.00287628 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86430709 | CAGGCTTCAATGTTA[A/G]CTGCAGAAAATGACC | 11059 |
rs776604277 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361475 | ACATATATTCCTTCT[C/G]TGCTGAAAATGTAGT | 11059 |
rs776621885 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383293 | TTTAACCATATTCCC[A/G]TTGTTGGACATCTAG | 11059 |
rs776632049 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450884 | GGGAGGAGTCAGGAA[A/G]GTTCTTCATAGGACA | 11059 |
rs776653446 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86421651 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11059 |
rs776692006 | in-del | -/TATTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86346992 | GTAATAACTGCTTTA[-/TATTT]TATTTTATTTTATTT | 11059 |
rs776704726 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86447555 | ACAAGTGTGAGCCAC[C/T]GCGCCCCACCTTGAA | 11059 |
rs776717408 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413867 | TCCTCTTTGCTTTTA[C/T]TAAGATCATTTTTGC | 11059 |
rs776721386 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395813 | TTGAGATCATTACCA[A/G]TACAAAATTATATGC | 11059 |
rs776725383 | snp | A/G | 1.68875e-05 | 0.00290576 | intron-variant | WWP1 | GRCh38.p7 | 8:86448325 | ATTTTTTTGAAACCC[A/G]TTTTGTTTCATTTTG | 11059 |
rs776726541 | snp | C/T | 4.95233e-05 | 0.00497586 | intron-variant | WWP1 | GRCh38.p7 | 8:86461742 | AAAAGTTTAAAGGAC[C/T]AGATAAACTTTGTCT | 11059 |
rs776789801 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380581 | TCTCAAGCATTATCA[A/G]TAGCCCTTTTGTATT | 11059 |
rs776792141 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442888 | GCTATTCACAAGTTT[C/T]GTTACCAAGAAAGTT | 11059 |
rs776800707 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413636 | CAGTAGAGCCGACTG[A/C]ACATTCAGATTCCTA | 11059 |
rs776806978 | in-del | -/T | 0.00125646 | 0.025033 | intron-variant | WWP1 | GRCh38.p7 | 8:86402005 | GATTGAAATAAGGCA[-/T]TTTTTTTTTCAAGGT | 11059 |
rs776815392 | snp | A/G | 1.70179e-05 | 0.00291696 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438639 | TATGTAATATTTAGA[A/G]GAGAAGAAGGACTTG | 11059 |
rs776817881 | in-del | -/TAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457247 | TTTGACAATTTCACA[-/TAG]TAGAATATTCCTAGA | 11059 |
rs776838235 | snp | C/T | 1.75789e-05 | 0.00296465 | intron-variant | WWP1 | GRCh38.p7 | 8:86425185 | AAGATTGTCCTAGTG[C/T]GTTGTCTCTTACTGT | 11059 |
rs776870210 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371915 | GACGTGACCTCAGCT[C/T]ACTGCAGCCTCCACC | 11059 |
rs776886305 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438979 | TTTTATATAGTGTGG[A/G]CATCTTTCTATGTTA | 11059 |
rs776925939 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86440400 | TTGCATAATGTTCTC[-/T]GTTGCTTTTACATAT | 11059 |
rs776935392 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86404926 | TCATCTTTTATACTG[C/G]TAGGCTTCACACAGC | 11059 |
rs776937131 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86386807 | TGAGACTAGGTAACT[C/T]ATGGAGAACATAAAT | 11059 |
rs776986605 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86389551 | AGTCTCTTATGTCTA[C/G]TTCTTTCTACACAGA | 11059 |
rs777033899 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459108 | GATCTCAGCTCATTG[C/T]ACCCTCTGCCTCCCA | 11059 |
rs777047769 | snp | A/C | 0.0023656 | 0.0343104 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452653 | CCTCTTCAGTGGCTA[A/C]AGTACTTCGATGAAA | 11059 |
rs777049011 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408207 | TAAGGTTTCTCCATG[-/T]TTTTTTGTGGCTTGA | 11059 |
rs777070749 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368139 | GTCATCTTTATTGAG[C/T]CTTTACTTCGTGTCA | 11059 |
rs777212287 | snp | C/T | 4.95569e-05 | 0.00497755 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381564 | ATCGCACTTTAAAAG[C/T]AGATGCTTTATTAGG | 11059 |
rs777227802 | snp | C/T | 1.77193e-05 | 0.00297647 | intron-variant | WWP1 | GRCh38.p7 | 8:86411878 | CTTGCCATCAGGGTA[C/T]GTTAAGCTTTTTAAT | 11059 |
rs777236577 | snp | C/G | 3.30251e-05 | 0.00406343 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425256 | TCCTCATGGTAGAAC[C/G]TATTATGTGGATCAT | 11059 |
rs777237450 | snp | A/G | 5.13589e-05 | 0.00506723 | intron-variant | WWP1 | GRCh38.p7 | 8:86398323 | AAAAGCTTTTAAATT[A/G]GAATATTCTTCTTTC | 11059 |
rs777269106 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408903 | TGACAGAGCAAGACT[C/G]TGTCTCAAAAAAAAA | 11059 |
rs777291038 | snp | C/T | 1.65094e-05 | 0.00287305 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381525 | TTACGCCACAGACTA[C/T]ATTGGAATTTCAAGT | 11059 |
rs777312589 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86410801 | GGCCATGTCCAGTAG[C/T]ATTTAATCTGAGTGT | 11059 |
rs777314179 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412675 | TTCATTTTGTTACCT[C/G]AGTCACTATGTTAGT | 11059 |
rs777341965 | in-del | -/AG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405853 | CTTTCTAAATTCCAA[-/AG]AGAAAGTTATGAATT | 11059 |
rs777369390 | snp | G/T | 1.66724e-05 | 0.0028872 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86425224 | TATTTTTATTAAAGG[G/T]GGGAACAAAGAAAAG | 11059 |
rs777380252 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380924 | ATTTTTTGGAATATG[-/T]TTTTTTGTTTTGTAA | 11059 |
rs777412229 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400264 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 11059 |
rs777422842 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86363744 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 11059 |
rs777448348 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383528 | AGGCGGATCACCTGA[A/G]GTCAAGAGTTTGAGA | 11059 |
rs777451505 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393736 | AATTCTGTTTTTCTC[A/T]TACTTTTGAGTATGT | 11059 |
rs777463226 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443190 | CGATCCTCCCACCTC[A/T]GCCTCCCAAGTAGCT | 11059 |
rs777474714 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349008 | TAGGGCTCACAAGAG[C/T]ACAAAACAGAAGCAA | 11059 |
rs777490968 | in-del | -/TAT | 1.65091e-05 | 0.00287303 | intron-variant | WWP1 | GRCh38.p7 | 8:86435615 | CAGATGATATTATGA[-/TAT]TATTTTTGTTTTTAG | 11059 |
rs777504729 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439808 | TTAGCAAAACATTTT[G/T]ATTAAATCTTTCTAA | 11059 |
rs777557253 | in-del | -/T | 8.78279e-05 | 0.00662618 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466744 | AAGTATTCTATTAGA[-/T]TTTTTTCATTTTATT | 11059 |
rs777572937 | in-del | -/TAAG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354379 | ATGCTTGTGTGTGGA[-/TAAG]TAAGGTTAATAAATA | 11059 |
rs777592651 | in-del | -/ATATATATATATATATATATATATAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362164 | ATATATATACAAGGC[-/ATATATATATATATATATATATATAT]ATATATATATATACT | 11059 |
rs777593997 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449007 | GCTAATTTAAAACAA[-/T]TTTTTTTTTTTTTGT | 11059 |
rs777602999 | in-del | -/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86399952 | TCAACAGATAGTTAC[-/TT]AATGCCTGTTTGATG | 11059 |
rs777645430 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466552 | TTTTTTTTTTTTTTT[-/A]AAATTTGTCTTTATC | 11059 |
rs777676610 | in-del | -/ATT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405326 | TCTGAAACCAAAAGG[-/ATT]TTTTTTTTTTTTTTT | 11059 |
rs777695716 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387896 | ATTTAAGCATCATTC[A/G]GTAAGGGCTGCTGTC | 11059 |
rs777697555 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427717 | CAACAACGTGGCAGC[A/G]GCCTACCATGGAATC | 11059 |
rs777698046 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385175 | AAGGTTATTGATAGA[G/T]ATATTATGTTTCTGA | 11059 |
rs777702857 | snp | C/T | 1.66955e-05 | 0.0028892 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411553 | TTAATGGAGAATCAT[C/T]CTCATTTGCACCAAC | 11059 |
rs777708680 | snp | C/T | 3.34857e-05 | 0.00409167 | intron-variant | WWP1 | GRCh38.p7 | 8:86435446 | TTTATTTTTGTTTTT[C/T]TTTAGAACTAAAGGT | 11059 |
rs777711133 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428403 | ACAAAACTCCTCTGA[C/T]AAATGGTGTGATCAT | 11059 |
rs777758049 | snp | C/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431740 | GCAATGGGAAGTCAT[C/G]TGTGTGAGTGAAAAC | 11059 |
rs777775031 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370855 | TAGCTATATTCATTC[-/T]TTTTTTTTTTTTTTT | 11059 |
rs777777787 | snp | A/G | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86452585 | AATGGCGTTTTTCTC[A/G]AGGAGTACAAGAACA | 11059 |
rs777811711 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406670 | TGTGTGTATGTGTGT[G/T]TGTGTGTTTCTATAC | 11059 |
rs777815572 | snp | A/G | 1.69743e-05 | 0.00291322 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448231 | AAAACTTACTATTAA[A/G]GATTTGGAATCTATT | 11059 |
rs777830977 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426609 | AGACTCTCACATGAG[C/G]CCCTTGTAGGATCTC | 11059 |
rs777849699 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359831 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 11059 |
rs777870601 | snp | G/T | 0.000109636 | 0.0074031 | intron-variant | WWP1 | GRCh38.p7 | 8:86448102 | TGTTCTCTAAGAAAT[G/T]GTTATTTTGCAAATT | 11059 |
rs777878304 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461426 | TTACTCTTCTGTGCT[A/G]TAGGTAGGGCTTCAT | 11059 |
rs777890266 | in-del | -/AAAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464070 | TGTCTCAAAAAAAAC[-/AAAA]AAAAGATCAAAAAGT | 11059 |
rs777905305 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86361579 | TCTCTCCCCATACCC[-/T]TCCTAACAGAACTAC | 11059 |
rs777935914 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420950 | TATGGGAATTATTAC[A/C]TAAAAATAGCAAAAG | 11059 |
rs777972060 | snp | A/G | 6.59217e-05 | 0.00574078 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402062 | GATAATCATGTACCT[A/G]CAAGCACTCTAGTCC | 11059 |
rs777989472 | snp | A/C | 1.65899e-05 | 0.00288005 | intron-variant | WWP1 | GRCh38.p7 | 8:86374023 | AAATTCCCCTTTTTT[A/C]AAATAGGTTTTAGCT | 11059 |
rs777997832 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464668 | CCACCAGTGCACGCC[A/C]CTATGCCTGGCTAAT | 11059 |
rs778004610 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86370075 | CTTACCTTTTCCCAG[C/T]CCCTAAAGTAAGTGC | 11059 |
rs778009356 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86429540 | TTTCTTCAGAATATA[A/T]TTCTAGGTTATAAGA | 11059 |
rs778010969 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445169 | ATTAGTCTATTAGTT[G/T]CAGGTCAAAATTCTT | 11059 |
rs778011536 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86353313 | AGCAGGATCCAAAAT[A/C]TGATCCTGTCATCAG | 11059 |
rs778058007 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86418082 | CATAAATAGAATCAT[A/G]CTGTATATAGTTTTT | 11059 |
rs778080699 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367069 | AAAATAGCTTTGCCT[A/G]AGTGCAGGCTTTCTA | 11059 |
rs778086010 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411629 | TGCCTTGTCTCCAAA[C/T]TGCACTAGTACTACT | 11059 |
rs778150675 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368490 | TCTTTCATGGTGCCA[A/G]TGCTCTAGTTCAGAT | 11059 |
rs778161874 | in-del | -/T | 1.65486e-05 | 0.00287646 | intron-variant | WWP1 | GRCh38.p7 | 8:86374129 | GTAACTGGTAAGTTA[-/T]TTTTATATTTAATAT | 11059 |
rs778195236 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457795 | GCTTATTGTGATCAT[C/T]ATATGCCATGCATAT | 11059 |
rs778206615 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432032 | TACTATTATTTTTCC[C/T]TTTACCAAGTGAGGA | 11059 |
rs778218287 | snp | A/G | 1.65329e-05 | 0.0028751 | intron-variant | WWP1 | GRCh38.p7 | 8:86398661 | ATTTTATTTGAATAT[A/G]GGTGGCGACATGATG | 11059 |
rs778228366 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86366123 | GAGAGTGCTGGAGAG[A/C]CTGTAGTTCCTGAGT | 11059 |
rs778236110 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86360169 | AAAAAACCAAACCAA[A/G]CCAATCCTCTAAACA | 11059 |
rs778273412 | snp | A/C | 1.67868e-05 | 0.00289709 | intron-variant | WWP1 | GRCh38.p7 | 8:86430646 | CTTATTTCTACTTTC[A/C]TATTAAAACACTGTT | 11059 |
rs778283523 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350747 | GTTCTTTTGATAGCT[C/G]TTCAGTATACTCATA | 11059 |
rs778286535 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462711 | ATTCTTTCAAGAGGT[C/T]AAAACTATTTTCATA | 11059 |
rs778287201 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426333 | TAGCGTCTATTATTC[C/T]CTTTGTGACCCCATT | 11059 |
rs778310751 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379288 | AGTAGCAGTTCAGAC[A/G]TAACATTGAACACTC | 11059 |
rs778342934 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457181 | GAGATTAAGTATTAC[A/G]TATTTTACTATACCT | 11059 |
rs778384754 | snp | C/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368734 | GCAAGCAGTTCTCTG[C/G]ATGTGCCGTTCTTTC | 11059 |
rs778384873 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86383353 | TACTGAACCTCCATA[G/T]AAAGATAACTATCCA | 11059 |
rs778434680 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341204 | ATTTAAAGGGACCAG[A/G]CAGCAAAAGCAAAAA | 11059 |
rs778437062 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422418 | CCCAGGCTGGAGTGC[A/G]GTGCAATCTTGGCTC | 11059 |
rs778437888 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369578 | GTTCCCCAGTTTGCA[C/T]AGTATTGTAAACTTT | 11059 |
rs778473795 | snp | C/G | 1.65165e-05 | 0.00287367 | intron-variant | WWP1 | GRCh38.p7 | 8:86431756 | TGTGTGAGTGAAAAC[C/G]TGAAGTTCTCCTTTA | 11059 |
rs778501502 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86415887 | ATTTTGTCTATTTCT[A/G]TATTCTTCGTGCTCA | 11059 |
rs778516761 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398454 | TGAGCAAGAAAATAT[A/G]ACAAACTGCAGCTCA | 11059 |
rs778527124 | snp | A/T | 1.65392e-05 | 0.00287564 | intron-variant | WWP1 | GRCh38.p7 | 8:86457877 | ATATAATTATTCTCT[A/T]CACTAAATCTTTATT | 11059 |
rs778546668 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414693 | TGTACAGCCAAGTTG[A/G]GAACTGCTACTTCAA | 11059 |
rs778555453 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430640 | GCTTGGCTTATTTCT[A/G]CTTTCATATTAAAAC | 11059 |
rs778595986 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411642 | AATTGCACTAGTACT[A/G]CTGTTGAAGATCCTC | 11059 |
rs778607877 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452098 | ACAATCCCTTGCCTT[A/G]CTGGTGTGGAAGGCT | 11059 |
rs778615644 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86465929 | GCTCTTTCCTGACTC[C/T]GACATGGGAGGGTCA | 11059 |
rs778623387 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86425099 | CTTTATATATATAGC[-/TG]TGTGTGTGTATAGTC | 11059 |
rs778629413 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460270 | TATTAAGAGTGGCAG[C/G]AGGGAGGTGTTCATT | 11059 |
rs778649126 | snp | A/G | 3.30393e-05 | 0.0040643 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435462 | TTTAGAACTAAAGGT[A/G]GTCCACAAATTGCTT | 11059 |
rs778652077 | snp | G/T | 1.66219e-05 | 0.00288283 | splice-acceptor-variant | WWP1 | GRCh38.p7 | 8:86427642 | TGTTTACTTGTGGTA[G/T]TTGGGAAAGAAGAGT | 11059 |
rs778680308 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462140 | TGCCCCATGGTGGGG[C/T]ACAAATGACAAACAG | 11059 |
rs778700144 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438881 | ATATGTAAATTTGTA[C/T]ATATGTGTAATATAG | 11059 |
rs778739340 | snp | C/G | 1.65272e-05 | 0.0028746 | | | GRCh38.p7 | 8:86411747 | GCTAGAAGTATATTA[C/G]AGCCTGACACCTCTA | 11059 |
rs778743913 | in-del | -/ATTTGGTTT | 1.80922e-05 | 0.00300762 | | | GRCh38.p7 | 8:86435425 | CTTTATTATGAGTTA[-/ATTTGGTTT]ATTTTTGTTTTTCTT | 11059 |
rs778789058 | in-del | -/CATATATATATATATA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430798 | AGATATATATCTCTC[-/CATATATATATATATA]TATATATATATATAT | 11059 |
rs778818636 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86427156 | TGACAAGAGCGAAAC[A/G]CCATCTCAAAAAAAA | 11059 |
rs778891189 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362615 | TTTAAGTAGTACATG[A/G]GCCCCAAATCTGTTT | 11059 |
rs778945934 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439588 | CATTCTTATTTTTTG[A/C]TATTGTAAGTAACAT | 11059 |
rs778961397 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86349316 | GAGCCACCGTGCCTG[A/G]TCTGCAACCAGATCT | 11059 |
rs778983748 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380616 | CTTCATTCTGCCAAC[A/G]AGAAGAGTTCTAGTT | 11059 |
rs778998623 | in-del | -/AC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457549 | ATACATAATAGATAC[-/AC]ACACACATTTAGATA | 11059 |
rs779001469 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367335 | TGACTTTTCAAAGTC[-/TT]AACACTGCAGAGTGT | 11059 |
rs779014326 | snp | A/G | 3.3065e-05 | 0.00406588 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448422 | TACTTTTCTGTTGAC[A/G]TGGAGATTTTGGGAA | 11059 |
rs779041282 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86443380 | CTCCCAGCCTACTTT[G/T]CAATAAAAGGAAAAT | 11059 |
rs779044709 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341411 | GAATGACACAGATGT[A/G]TATTTTCGAATGATC | 11059 |
rs779065156 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456988 | TTGTTTTGATTACAA[A/C]AAGGGGATGATGATT | 11059 |
rs779108247 | in-del | -/ATAAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86356599 | TTATCTTTTGTTGAC[-/ATAAT]AGAGTAACGATGCCA | 11059 |
rs779117705 | in-del | -/A | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341911 | AGTAGAAACCGGGTC[-/A]CCTGGTAAGCAATGT | 11059 |
rs779134007 | snp | A/G | 1.70084e-05 | 0.00291615 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438617 | CTATGACTTGAGGAG[A/G]CGCTTATATGTAATA | 11059 |
rs779144633 | in-del | -/CACTTAC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395610 | TCATTTCCTTCAATG[-/CACTTAC]CACTAAAAGAATGTT | 11059 |
rs779157252 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385646 | CATGGTTTAGTGATA[A/G]TGGGAAAGTTATTGT | 11059 |
rs779170875 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348279 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCAC | 11059 |
rs779186268 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86442326 | TGTTGAAATGGGATT[G/T]AAGCTGAATTGAAGT | 11059 |
rs779234278 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377760 | AGGAAACTGTCAGAA[A/G]CATAGAGTATGCAAG | 11059 |
rs779260243 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86436070 | CATTTGCAAAACACC[A/G]GCATCTTACATTTCT | 11059 |
rs779280483 | in-del | -/GGGGCTGCCCCCATAAGCGCTAACTTAAGTTAGCGCTTAT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423941 | GCGGCTGGCCGGGCG[lengthTooLong]GGGGCTGCCCCCCAC | 11059 |
rs779282728 | snp | C/T | 3.30022e-05 | 0.00406202 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402157 | TGCCAGACCCAAAAA[C/T]ACACCAGCTCCAAAA | 11059 |
rs779305034 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412981 | TTAGAGGCACCCGCC[A/G]CTATGCCCAGCTAAT | 11059 |
rs779317283 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86388089 | ATACATGGCCGCTGG[-/C]CTACTGTATTGGTCA | 11059 |
rs779329320 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86357796 | TTTGATTTTGCAGGA[A/G]CAGTGTATATGCACA | 11059 |
rs779336984 | snp | G/T | 6.63372e-05 | 0.00575884 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380833 | AAATCCAGTAGTTCT[G/T]CTAATCCAAAATGGG | 11059 |
rs779354616 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86417963 | TTATGTAAAAAAACT[C/T]GTTGAGTAATGTCCG | 11059 |
rs779370099 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376940 | CTCACAATAACTTCT[G/T]CAATAAAGATTACTA | 11059 |
rs779382495 | snp | A/T | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86341802 | AGGAAAACTAGTAAG[A/T]CTGGGTGTGGACGTA | 11059 |
rs779400493 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86393518 | AAAGTGCTGGGATTA[C/T]AGATTTATTATAAAT | 11059 |
rs779438301 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394656 | CACTCAAATATTGAA[C/T]GGATAAATACATCGG | 11059 |
rs779460630 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461801 | CTCAAAAGTTTTGCA[C/T]TGAAAAAGTTGGCAA | 11059 |
rs779463662 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381553 | AGTTTGGAGCCATCG[C/T]ACTTTAAAAGCAGAT | 11059 |
rs779485855 | in-del | -/TG | 1.6757e-05 | 0.00289452 | intron-variant | WWP1 | GRCh38.p7 | 8:86430658 | TTCATATTAAAACAC[-/TG]TTATTTTATTTCTCT | 11059 |
rs779502188 | in-del | -/GTG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86380445 | GTTTTAAAATTGATT[-/GTG]GTGATGGTTGTGCCA | 11059 |
rs779513617 | snp | G/T | 1.65181e-05 | 0.00287381 | intron-variant | WWP1 | GRCh38.p7 | 8:86461354 | TAATTTCTCTGTACG[G/T]AATTTTGTGATAATA | 11059 |
rs779590886 | snp | A/G | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86435486 | ATTGCTTATGAACGC[A/G]GCTTTAGGTGGAAGC | 11059 |
rs779594013 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379898 | TGAGAATGTGGAGAA[A/G]TCAGTGTATATTGTT | 11059 |
rs779639526 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86407089 | TGGGAGATGTTCATT[C/G]AGAACCCAAGTCAGT | 11059 |
rs779645144 | snp | A/G | 1.65872e-05 | 0.00287981 | intron-variant | WWP1 | GRCh38.p7 | 8:86461195 | ATAGTTTAGCATTTC[A/G]TATTAAAGTACATTT | 11059 |
rs779652389 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86463552 | ACCTTGTGATCTGCC[C/T]GCCTTGGCCTCGCAA | 11059 |
rs779668252 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402537 | CCTCAAGTGATCTGC[C/G]CACCTCAGCCTCCCT | 11059 |
rs779675593 | snp | A/G | | | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438637 | TATATGTAATATTTA[A/G]AGGAGAAGAAGGACT | 11059 |
rs779691905 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368122 | CACAATAAAAACAAT[-/AA]GTCATCTTTATTGAG | 11059 |
rs779701683 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459722 | CGTTGTTTGTAATCT[A/T]CCCTTTCAGGCTTTT | 11059 |
rs779723300 | in-del | -/TAA | 0.000115876 | 0.00761081 | intron-variant | WWP1 | GRCh38.p7 | 8:86381485 | CTCCTGTATTTTTGT[-/TAA]TAATTTTACCCTTCC | 11059 |
rs779777313 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412239 | AGACCTCATACTGGA[G/T]AGCAAATAGCTCTTC | 11059 |
rs779784633 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86426916 | TAATCCCCACACTTT[-/G]GGGAGGCCAAGAGGT | 11059 |
rs779787218 | snp | A/C | 1.65581e-05 | 0.00287728 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411760 | TAGAGCCTGACACCT[A/C]TAATTCTAGAAGTAG | 11059 |
rs779794031 | snp | A/G | 1.65083e-05 | 0.00287296 | missense, intron-variant, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86398637 | GCAAGGACAACTGCC[A/G]GGTAGAATATTTTAT | 11059 |
rs779840878 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354028 | ATTAACGTATTGGCT[A/G]TTTAGAGCTCGGGCC | 11059 |
rs779854460 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450260 | TCATCTCTGAGTGAG[A/G]GAAGTTACCAATAAC | 11059 |
rs779857907 | in-del | -/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364832 | AGAAAGAAAGAAAGA[-/G]AAGAGAGAGAGAGAG | 11059 |
rs779866289 | snp | A/T | 1.65677e-05 | 0.00287812 | intron-variant | WWP1 | GRCh38.p7 | 8:86381471 | AATGACAACGTCTAC[A/T]CCTGTATTTTTGTTA | 11059 |
rs779872032 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86460445 | TCCATTTCCTTATAT[G/T]TACAGTGGGGATGCT | 11059 |
rs779890636 | snp | A/C | 6.60633e-05 | 0.00574694 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448444 | TTTTGGGAAAAGTTA[A/C]TTCACATGACCTGAA | 11059 |
rs779899225 | in-del | -/CT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378383 | GTTCTCTTCATGTGA[-/CT]CTTACTTATTTCTTA | 11059 |
rs779921371 | snp | C/T | 0.000134183 | 0.00818985 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411831 | TGTATGGATCCTGTA[C/T]GGCAGCAGTCTGGGA | 11059 |
rs779942241 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86467133 | TTGAAGCAAGTGAGA[A/G]ACTTTATTAAAAATA | 11059 |
rs779948647 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416786 | AGTTGAGGGGTGTTC[A/G]TGAATTTTCACTACG | 11059 |
rs779964250 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86452453 | TATATGTTTATATAT[A/G]TGGCATATTTAGAAA | 11059 |
rs780022183 | snp | A/G | 4.95054e-05 | 0.00497496 | intron-variant | WWP1 | GRCh38.p7 | 8:86431499 | CTCAAGGGTATGTAT[A/G]TACAGCAGCCTTAAG | 11059 |
rs780024492 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396403 | TGCGCCTGGCTGCTT[A/T]TGTAGTTTTTGTGTG | 11059 |
rs780062997 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86444790 | TATAAACAAGGAATC[A/T]TAGAGAATTGGTCAC | 11059 |
rs780077500 | snp | A/C | 3.34325e-05 | 0.00408842 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402175 | ACCAGCTCCAAAACC[A/C]CTCGCATCTGAGCCT | 11059 |
rs780092038 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86451740 | CTCTTCATCGTCTAG[A/T]ATCTGTGGCTTCTCT | 11059 |
rs780095949 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376806 | GGGAAAGAATGATCA[C/T]GGACCTGTGCTAAAT | 11059 |
rs780130440 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86402094 | AAACTCATGCTGCTC[A/G]TATGTAGTTAATGGA | 11059 |
rs780147811 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86343807 | TAACAAATTTTTTTC[-/TG]TGTGTGTGTAGGTTA | 11059 |
rs780186637 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456772 | TATTCAGTGATAGAA[A/G]ATATGAACTACTGGT | 11059 |
rs780235539 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86430361 | TCACAGTTCACTGTA[G/T]CCTCCACCTCCTGGG | 11059 |
rs780327733 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86461061 | TGATCCGCCTGCTTC[A/G]GCCTCCCAAAATGCT | 11059 |
rs780354517 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86416801 | ATGAATTTTCACTAC[A/G]GGATTATCTGGTCTC | 11059 |
rs780378522 | in-del | -/GC | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462805 | TGTGAACCTGCTTGT[-/GC]CTTAGCACAAATCAA | 11059 |
rs780445634 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408510 | ATCTCACCAACATTT[G/T]CATTTCAAGGAGAGT | 11059 |
rs780469680 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434218 | ATTTGCACAAAACCC[G/T]TCAGTGGTTTCCATC | 11059 |
rs780490492 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392182 | GGAGGAAATCATTTG[C/T]GCTGAGTTTGCAGTT | 11059 |
rs780563516 | snp | A/T | 1.66073e-05 | 0.00288156 | intron-variant | WWP1 | GRCh38.p7 | 8:86442788 | GCCATGGTGAGTTCC[A/T]GACTTTATTATTATT | 11059 |
rs780565302 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354763 | TACTTTTCTCTATAT[C/T]GTTGTGGAAGTATGG | 11059 |
rs780600206 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400819 | ATAGGTTAGAGAGAA[C/G]ATGGGATAAAGGTGT | 11059 |
rs780600410 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86396289 | TATTTTTTGTAGAGA[C/T]GGGGTTTCACCACGT | 11059 |
rs780614026 | in-del | -/A | 1.67857e-05 | 0.00289699 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86380747 | TGCCAAACTTAAAAG[-/A]AAAAAAGAACTGGTT | 11059 |
rs780616174 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86355665 | ATCTCTAACAGCTTA[C/T]CTACTCCATTGTTTA | 11059 |
rs780618306 | snp | A/T | 1.65674e-05 | 0.00287809 | intron-variant | WWP1 | GRCh38.p7 | 8:86442568 | ATTTAAGATCTGTTT[A/T]TAAATTCACATATTA | 11059 |
rs780658806 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86413283 | TTGTCCTGTGTCCCA[C/T]GTTTGGTAAATTAGT | 11059 |
rs780664094 | snp | C/T | 1.67136e-05 | 0.00289076 | intron-variant | WWP1 | GRCh38.p7 | 8:86435731 | TTTAGCAGAATAAAA[C/T]ACCATTTGTCTCATT | 11059 |
rs780667679 | snp | C/T | 1.69689e-05 | 0.00291275 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438624 | TTGAGGAGGCGCTTA[C/T]ATGTAATATTTAGAG | 11059 |
rs780671317 | snp | A/C | 1.70321e-05 | 0.00291818 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86411853 | AGTCTGGGAATGCCA[A/C]CACAGAAACCTTGCC | 11059 |
rs780686933 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439387 | TTGTAGAAATGAGGG[C/T]CTCACAGTTTTGCCC | 11059 |
rs780718987 | snp | A/G | 1.6513e-05 | 0.00287336 | intron-variant | WWP1 | GRCh38.p7 | 8:86461351 | CTGTAATTTCTCTGT[A/G]CGTAATTTTGTGATA | 11059 |
rs780733797 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86395187 | ATTAGTTTAAGCTAA[C/T]GTCAGAGAATAAACA | 11059 |
rs780734348 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86344613 | AATCCTCTCAGAAGT[C/T]AACTTCAAAGAGAGT | 11059 |
rs780737025 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86466124 | CTAGCTACTCAGTGC[C/T]GTACCTCACAAAACG | 11059 |
rs780744979 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86350208 | GCTATCTGGGTTTTT[-/C]CTCGCATTATCACTT | 11059 |
rs780750028 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86419340 | GAAGAATCGCTTGAA[C/T]CTGGGAGACGGAGGT | 11059 |
rs780783840 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450047 | CTAGATTTTTAAAAA[A/G]TGAAGTTACTGGGTC | 11059 |
rs780784245 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86405271 | TAACATAATTAAATG[C/T]TTTTAATCTCTTAAT | 11059 |
rs780785531 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1, LOC105375624 | GRCh38.p7 | 8:86346335 | GGCTGAGGCAGGAGG[A/G]TGGTGTGAACCCGGG | 11059 |
rs780803256 | snp | C/G | 1.71658e-05 | 0.00292961 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86438601 | TTATGGCATTAAAAC[C/G]CTATGACTTGAGGAG | 11059 |
rs780808049 | snp | A/G | | | upstream-variant-2KB, intron-variant | WWP1, LOC105375624 | GRCh38.p7 | 8:86342073 | GTGCGTTAATTGTGC[A/G]GACACGTATACTCGG | 11059 |
rs780817543 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377318 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCACAG | 11059 |
rs780854759 | snp | C/G | 3.29788e-05 | 0.00406058 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86461793 | TAATGGGCCTCAAAA[C/G]TTTTGCATTGAAAAA | 11059 |
rs780958519 | in-del | -/TTTG | 1.69591e-05 | 0.00291191 | intron-variant, downstream-variant-500B | WWP1, RMDN1 | GRCh38.p7 | 8:86466779 | ACATCTGATTTTGTT[-/TTTG]TTTCTGTTCAGTTTT | 11059 |
rs780980418 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437296 | GAAAATTTGGTATAC[A/G]TATTGTTTTTAAGTT | 11059 |
rs780983666 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86428137 | AATCTTCCACTTTTA[C/T]AAATTTTGTTTGCTT | 11059 |
rs781031567 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86438505 | TGTTATTTTGAAAAT[A/G]GAGATTAAATTTAAA | 11059 |
rs781047134 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, utr-variant-5-prime, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86381507 | TTTACCCTTCCAGAA[A/G]TGTTACGCCACAGAC | 11059 |
rs781052732 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86359594 | ACATTTTCAAAGATA[A/G]GCATTCTTTTCTCTT | 11059 |
rs781164686 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86387589 | GCAGTCTCGGCTCAC[C/T]GCAGCCTTTGCCTCC | 11059 |
rs781170743 | snp | C/T | 3.34169e-05 | 0.00408746 | intron-variant | WWP1 | GRCh38.p7 | 8:86452556 | TACCATCTTTATTTT[C/T]AGTTTAATGACAGAA | 11059 |
rs781174374 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86412142 | AATTTGATTCTTGGT[C/T]TATTTCTACTTTTCG | 11059 |
rs781189470 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86351506 | AACATGCTCAGCTAG[-/T]TTTTTTTTTTTTTTA | 11059 |
rs781215320 | snp | C/T | 1.66076e-05 | 0.00288158 | intron-variant | WWP1 | GRCh38.p7 | 8:86374014 | CACATGAATAAATTC[C/T]CCTTTTTTAAAATAG | 11059 |
rs781224009 | snp | A/G | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86448464 | CATGACCTGAAGTTG[A/G]GAGGTTCCAATATTC | 11059 |
rs781226827 | in-del | -/TCTG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86457414 | GGGGAGATCTATCTG[-/TCTG]TCTGTCTGTCTGTCT | 11059 |
rs781241471 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433229 | TTTTTTCCTAAGCCT[-/C]TTTTTTTTTTTTTTT | 11059 |
rs781246583 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86378601 | CTACTAACTAGAACA[A/G]CTTTTTGAATTAATA | 11059 |
rs781272808 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462386 | AAGACCCCGAAGAAA[C/T]TGTTTTTCAAGGAAA | 11059 |
rs781320893 | snp | C/G | 4.98782e-05 | 0.00499366 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86466944 | AAATACCCCAGCCAA[C/G]AAAAATTGCACAGAT | 11059 |
rs781414117 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86362996 | ATGCTTAATAATTTA[A/G]CATTTATATAGTACT | 11059 |
rs781436222 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86434003 | GAATTCTAGTTACCT[C/T]AACTTCAAAACATAT | 11059 |
rs781489428 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86449323 | GTCCAAACATTTTCA[A/G]GAAAGAACCAGGCAG | 11059 |
rs781497511 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86431724 | ACATTCAAAGATCCT[C/T]GCAATGGGAAGTCAT | 11059 |
rs781545950 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86459517 | TTTGAAAAGGCAGAG[A/C]AAAAACTGGAAACAG | 11059 |
rs781609195 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86408267 | CACTTATTATAAAGG[A/C]TCCTTGGTTACTTCA | 11059 |
rs781626074 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406837 | AACTTGCTGTGTATA[C/T]GCAAGCAGTCATTTC | 11059 |
rs781679282 | snp | A/G | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86367317 | TATGTGACAGCATTT[A/G]TTTGACTTTTCAAAG | 11059 |
rs781686880 | snp | C/G | 3.30267e-05 | 0.00406353 | synonymous-codon, nc-transcript-variant | WWP1 | GRCh38.p7 | 8:86427811 | TAACCAACGATACCT[C/G]TATTCGGTAATTAGC | 11059 |
rs781693542 | snp | A/C | 1.7056e-05 | 0.00292022 | intron-variant | WWP1 | GRCh38.p7 | 8:86442821 | TTTAAGTTTGTTACA[A/C]ATGTATTAGAGAAGG | 11059 |
rs781708883 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86420277 | CTAATGAGCTTGAAC[A/G]TTTTAAGAGGAGATT | 11059 |
rs781712433 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391134 | TTTGTATTGTTTTCC[A/C]CAGAATCCAACTAAC | 11059 |
rs781718102 | snp | C/T | | | intron-variant, upstream-variant-2KB | WWP1 | GRCh38.p7 | 8:86368414 | CAGATTCTTGTTTTT[C/T]TGTAACCCTCAGCCA | 11059 |
rs781727642 | snp | A/T | 0.000205233 | 0.0101279 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | WWP1, RMDN1 | GRCh38.p7 | 8:86468443 | AGAATTAAAAAAAAA[A/T]TTCTAATGTATGTGA | 11059 |
rs781747642 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354585 | ATGCTTAGGAAGAGT[A/G]TTTGTAAATAGTGAA | 11059 |
rs796092476 | in-del | -/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86377269 | TTTTTTTTTTTTTTT[-/T]GTATTTTCAGTAGAT | 11059 |
rs796111411 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86376609 | GAAAAAGAAAAACCT[A/G]ATCTGGCTAATTTGA | 11059 |
rs796140558 | in-del | -/GT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86464931 | CGCGCGTGTGTGTGT[-/GT]ATTGAGAGAGAGATT | 11059 |
rs796190095 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456387 | ATATTAACAAAAAAA[C/G]TCACGTAACTCAATA | 11059 |
rs796231760 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86369382 | ATTTTTTAACTATCT[C/T]TCATGGTTTTAGTTT | 11059 |
rs796258335 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86348239 | CTTTTTTTTTTTGAG[-/A]CGGAGTTTCCCTCTT | 11059 |
rs796281288 | snp | A/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86384206 | GAGTCTCTAAAAACG[A/T]CACATTTTGAGGTAC | 11059 |
rs796290890 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86371217 | TCATTCGTTCTCACT[A/G]CTATATAATGCTCCA | 11059 |
rs796318518 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86458858 | TATACTTCAACGTGT[A/G]TAAAGTGGCACATAC | 11059 |
rs796328046 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86391455 | CACCAGTGTGAGATA[C/G]TGATATCTGAGGTAT | 11059 |
rs796349100 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364837 | AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 11059 |
rs796365679 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86354120 | TTAAGTTAACTTCAG[A/G]TTAAGCCCTAGTTTT | 11059 |
rs796399106 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439357 | CAAAAAAAAAAAAAA[-/A]GTTTTTAAAGCTTTT | 11059 |
rs796400668 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86402974 | GTTTATTTTCCAAAA[G/T]TAAGCATTACTGTAT | 11059 |
rs796413599 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86400401 | GCTAATTAGACATAG[C/T]GATAAGCACTATGAA | 11059 |
rs796426891 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86439342 | GCAAGACGCTGTGTC[-/A]AAAAAAAAAAAAAAA | 11059 |
rs796430481 | in-del | -/AA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364832 | AAGAAAGAAAGAAAG[-/AA]AGAGAGAGAGAGAGA | 11059 |
rs796454840 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86462879 | CCTTGAGGTTTAAAG[-/A]AAAAAAAAAAAAAAG | 11059 |
rs796462530 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86422206 | ATACTCTCTCATGTC[A/G]CTTCCGAAACACTGC | 11059 |
rs796490549 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379467 | TATATCCTTAACATC[C/T]GGTGTGTATGACATG | 11059 |
rs796532836 | multinucleotide-polymorphism | GA/TT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456407 | TAACTCAATAAAAAG[GA/TT]AAGAAAACATTTTTA | 11059 |
rs796547639 | in-del | AGT/GG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86358479 | CACATTTATTGAGGA[AGT/GG]TTTTTTTTTTTCCTT | 11059 |
rs796549196 | in-del | -/TA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414248 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTGTATGTAA | 11059 |
rs796559745 | snp | G/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86433732 | GCAGATCACCTGAGG[G/T]CAGGAGTTCGAGACC | 11059 |
rs796607451 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409847 | TCTGGGCCACAGAGC[A/G]AGACACCTTCTCAAA | 11059 |
rs796637039 | snp | C/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86456715 | TGTTCATTAACAAGT[C/G]AATGGATAAGCAAAT | 11059 |
rs796641390 | in-del | -/CTAA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375659 | ATAGATGTAAAAAAG[-/CTAA]CTAGTCTCCTTTTGC | 11059 |
rs796707863 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86406521 | AAGTTGCAAAGAAAT[A/G]TATGGGAAGGTCCCA | 11059 |
rs796733145 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86423940 | GGCGGCTGGCCGGGC[A/G]GGGGCTGCCCCCATA | 11059 |
rs796735815 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401565 | AAAAAAAAAAAAAAA[-/A]GTTTACAGTAGTTTA | 11059 |
rs796801719 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86375433 | CTTGCCCTGTAGGTT[C/T]ACATTTTTATTAGTT | 11059 |
rs796820980 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86409226 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 11059 |
rs796831022 | snp | A/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86379244 | TTGGAACGATGAAGG[A/C]TGGAAATGAGTTTTG | 11059 |
rs796843246 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86392443 | GATAATTAGACTGAG[A/G]TTTTTTATTTATTTT | 11059 |
rs796846832 | multinucleotide-polymorphism | CAT/TCA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414888 | CTGAATCCCCCCCCC[CAT/TCA]CCCCCACCCCCGCCC | 11059 |
rs796854350 | snp | A/G | | | intron-variant | WWP1 | GRCh38.p7 | 8:86437600 | TACTAGAAGGAGGAA[A/G]GAGTATAGTTGACCC | 11059 |
rs796871967 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86373494 | CCACCCCATGTAGAC[C/T]GTGAATTTTATTTTG | 11059 |
rs796885257 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86432598 | ACCAATGTGTTCAAT[C/T]GCAGTTCATTTTTTT | 11059 |
rs796913193 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86450423 | ATCATGCATAAGGCA[C/T]TGGACTTTCTATATT | 11059 |
rs796913870 | in-del | -/A | | | intron-variant | WWP1 | GRCh38.p7 | 8:86385037 | TCAAAAAAAAAAAAA[-/A]GTAAACAACTGCCAA | 11059 |
rs796916252 | in-del | -/C | | | intron-variant | WWP1 | GRCh38.p7 | 8:86445971 | CTTTTCTTTTCTTTT[-/C]TTTTCTTTTTTTTTT | 11059 |
rs796922910 | snp | C/T | | | intron-variant | WWP1 | GRCh38.p7 | 8:86372273 | GTGATCCGCCCGTCT[C/T]GGCCTCCCAAAGTGC | 11059 |
rs796946172 | in-del | -/TG | | | intron-variant | WWP1 | GRCh38.p7 | 8:86414228 | GAAAGTTTGTTTTTC[-/TG]TGTGTGTGTGTGTGT | 11059 |
rs796956615 | in-del | -/GTT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86394895 | ACAAATCTTTGTGGC[-/GTT]GATGATTTTGCAAAA | 11059 |
rs796981266 | in-del | -/AT | | | intron-variant | WWP1 | GRCh38.p7 | 8:86401863 | CATTTTACTTGAAAC[-/AT]AAAAACTCAATTGTT | 11059 |
rs796989194 | in-del | -/AA | | | intron-variant | WWP1 | GRCh38.p7 | 8:86364829 | AGAAAGAAAGAAAGA[-/AA]GAAAGAGAGAGAGAG | 11059 |