SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs558515136 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687992 | GCCGAGATGGCGCCA[C/T]TGCTCTTCAGCCTGG | 11137 |
rs558608439 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PWP1 | GRCh38.p7 | 12:107691679 | GGTTTCCATCTTATT[A/G]TCGCTGGTGTACCTC | 11137 |
rs558892746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704882 | TAGGGTTGAAAGCAT[A/G]AGGTGTTTTTTTTTA | 11137 |
rs558991155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699220 | GCTGAGATCGTGCAA[C/T]TGCACTCTAGCCAGG | 11137 |
rs559161612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107686498 | TAATCCAAGTGAGAT[A/G]TTGATGGTAGCAGGG | 11137 |
rs559288529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107710818 | ATAGCAAAAGTAGTG[A/T]AGTCTTTTTAGGAAA | 11137 |
rs559377180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693332 | CCTGGAAATTTTTCA[C/T]AGGGGTGTTTTTTTT | 11137 |
rs559427766 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PWP1 | GRCh38.p7 | 12:107688015 | AGCCTGGGCAACAGA[-/G]GCGAGACTCCGTCTC | 11137 |
rs559772005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691389 | GTGTGTTCTCTGTGC[A/G]AGAGGAAATCATTAA | 11137 |
rs559856890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698244 | GTGTGTTCCTGTAAT[C/T]CCAGCTACTTGGGAG | 11137 |
rs560109471 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694318 | GAAACTTTGAAGATT[C/T]GAAGAGATTATTAGG | 11137 |
rs560148061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107712020 | ACCATTTATAAAGTA[C/T]TAAGTGCACAATTCT | 11137 |
rs560192937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704322 | CCTGGCTCTGAGCTC[A/G]GCCAGAGAAGGGGAA | 11137 |
rs560205432 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685759 | GAAATGAGCGCCGAC[G/T]CTGCCCAAACAGGAG | 11137 |
rs560278030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703856 | TGAGGCCACCTTTAT[A/G]TTTAAATTATTTGCA | 11137 |
rs560315258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709879 | TAAGTGCATAATTGC[C/T]TAAATGCTTACATTT | 11137 |
rs560469080 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684086 | TTAAACCTCTTTTTC[A/T]TTATAAATTATCATG | 11137 |
rs560514513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689857 | GTGAGCTGAGATGAC[A/G]ACTACCTATATTGCT | 11137 |
rs560739292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702403 | CTCGTGCCTCAGCCT[C/T]CTGAGTAACTGGGAT | 11137 |
rs560753184 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705533 | CCTCCCCCCACCCCA[C/T]GACAGGCCCCAGTGT | 11137 |
rs560811665 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107706022 | TCCCACCAACAGTGT[-/A]AAACTGTTCCTATTT | 11137 |
rs561073813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711045 | TCAGAGCAGACAGCC[C/T]CGAACAGAGATTTAC | 11137 |
rs561081211 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704087 | ACGGGGTTTATAGCT[C/T]ATATCAGTGCTCCTT | 11137 |
rs561118799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697235 | TCAAATTGTGGCCCA[A/G]AGACCAGCAGCAGCA | 11137 |
rs561171583 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684106 | AAATTATCATGTCTT[A/G]GGTATGTCTTTATTA | 11137 |
rs561171729 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702744 | ATGGGGTTTCTTTCC[A/G]CTTATTTAGATACTC | 11137 |
rs561210335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690532 | GCTGTAGTGCAATCT[C/T]GGCTCACTGCAGCCT | 11137 |
rs561246047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703104 | AAAATAATCCCAAAC[A/G]TTTATATATGGCTTT | 11137 |
rs561280840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702433 | TTACAGGCATGCGCC[A/C]CCATGCCCAGCTAAT | 11137 |
rs561482165 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692286 | AATTTAAGTTCAGTG[C/G]AAAAAGCATACTGCA | 11137 |
rs561569476 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688082 | AGGACTCATGTAAGG[C/G]TGATTTGTTAAGGAA | 11137 |
rs561746846 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107708525 | CACACTGGTCGATTT[A/G]ACTGTTGGTCACGCC | 11137 |
rs561811700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695373 | TTTGAACATGAATTC[C/T]CATCACAGGGATGTG | 11137 |
rs561892640 | in-del | -/TG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688562 | ATGACCATGTGGTCT[-/TG]TTATTAGAAGGTAGC | 11137 |
rs561995001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107688292 | GAATCTATAAAATCT[A/G]TATTTTTTAATATAG | 11137 |
rs562009404 | in-del | -/AAA | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107687735 | CATGCCACATCTCTT[-/AAA]AATTAAAATTAAGGC | 11137 |
rs562086774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694947 | TCTCACGTGGTTAAG[A/G]GTATATTTTAAAGTA | 11137 |
rs562162942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107707608 | GTTTTAGCATGAAGG[A/G]CTGTTGAATTTTGTC | 11137 |
rs562195997 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712638 | GAACAGAGGCAAGTG[A/C]CCCAGAGACTCCACT | 11137 |
rs562359270 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690755 | AGGGAGAGTCGAAAA[C/T]GACATTGAGGAAATA | 11137 |
rs562399702 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711636 | GAGGTAGTCTGGTGC[A/G]TTCTACAAACACAGA | 11137 |
rs562485978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709749 | ATATAAGTTAGACTG[C/T]AGACACAGTAACACT | 11137 |
rs562509373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703147 | ATCTGGCTTGCGGCA[A/T]GCTTTCACATGTTAT | 11137 |
rs562596811 | snp | A/G | 3.29755e-05 | 0.00406038 | missense | PWP1 | GRCh38.p7 | 12:107709158 | CTCGTGACTGCTTCA[A/G]CTGACAAATACGTGA | 11137 |
rs562699770 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699481 | AAGACTGTAGCCATT[A/G]TGATCTTACCTCATG | 11137 |
rs562841748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107689129 | TCCATATACCTTTTC[C/G]TCAACTGCAGTCAGT | 11137 |
rs562875415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708256 | CACCTGCTTCCCTCT[C/T]ATCTCAAAAGAAGAG | 11137 |
rs563031882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701766 | CACTGCACCCCCCAC[C/T]TCTGGGGTTCAAGTG | 11137 |
rs563118132 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PWP1 | GRCh38.p7 | 12:107707794 | ATGTGCTGCTGGATT[C/T]GGTTTGCCAGTATTT | 11137 |
rs563149174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708838 | CACCAGTAAGTCATA[C/T]AGCTGATTTTCACTA | 11137 |
rs563153926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700899 | TTTAATTTGCATTTC[C/T]CCCCCTTTTTTTAAG | 11137 |
rs563553678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705536 | CCCCCCACCCCACGA[A/C]AGGCCCCAGTGTGTG | 11137 |
rs563810427 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685821 | CTGTGCAGATCCCTG[A/G]GCGTGTGGCAGCAGT | 11137 |
rs564258184 | in-del | -/A | 0.141258 | 0.225111 | intron-variant | PWP1 | GRCh38.p7 | 12:107695265 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAGTT | 11137 |
rs564327009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700562 | TAATGTATGTTACCC[A/G]TTCATTTACGTGTGG | 11137 |
rs564476666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706692 | TTTTGTCAGGTTTGT[C/T]AAAGATCAGATGATT | 11137 |
rs564562208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706034 | TGTAAAACTGTTCCT[A/G]TTTCTCCACATCTCT | 11137 |
rs564754480 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PWP1 | GRCh38.p7 | 12:107686837 | CGGGTGTGGTGGTGG[A/G]TGCCTGTAGTCCCAG | 11137 |
rs564797453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107687537 | GTCTGGGAACCACTA[C/T]TTGAAGAGTTTATAG | 11137 |
rs564822939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686468 | GCTGGGAGATGAATA[G/T]GGAATTTCTTGCAGT | 11137 |
rs564973300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699584 | CAGGCAGGAGCTCTG[C/T]CATCTGTTTCTTTGC | 11137 |
rs565060461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705445 | TTACATATGTATACA[C/T]GTGCGATGTTGGTGT | 11137 |
rs565107222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107691296 | AGCACAGAGAAGGTG[A/G]ATGGGCAGTTGCTGG | 11137 |
rs565449950 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684207 | CTACTGGTGGGCAGT[C/G]GGGGAGTGGGTGGGG | 11137 |
rs565471262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703805 | TCTAGAAGTCATTTT[A/C]AGAGTATCACTTGGT | 11137 |
rs565484188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698106 | GTGGCTCACTCCTGT[A/C]ATCCCAGCAGTTTAG | 11137 |
rs565627004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107699028 | CAACACTTTGGGAGG[C/T]CGAGAGTGGATCATG | 11137 |
rs565710999 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | PWP1 | GRCh38.p7 | 12:107689163 | TCACAATACAGTAGT[-/C]CCCCCCTTATCCACG | 11137 |
rs565760279 | snp | A/T | 1.65916e-05 | 0.00288019 | intron-variant | PWP1 | GRCh38.p7 | 12:107704772 | CGAATGTTGTTGTTT[A/T]GCTTTTCTAGGTTGC | 11137 |
rs565798839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710549 | CACCTCCCCCTGCCC[C/T]TGTAAAAAAAAAAAA | 11137 |
rs565798952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704164 | AAACCAACTTTGCAG[A/T]CTTTATTTTCATTTC | 11137 |
rs565833060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691561 | GGGCCTGGCTTGGGG[C/G]ACTAGGAATGAGGAG | 11137 |
rs565845892 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686045 | CCCAGCTGGGGGAAC[G/T]TGGACCCGGAACTCG | 11137 |
rs565868148 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696739 | AGAGTTCTTAACACA[C/T]CATCACTTTATTGTT | 11137 |
rs565869685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692133 | TCTCGTGTAGCAGAA[A/G]TTGCTTTCTCTGTTG | 11137 |
rs565870213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698610 | TTTTAAAGAGGTAAG[C/G]TCTTGCTCTGTCTCC | 11137 |
rs565891454 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685608 | AAGCCCGCAGGCATC[C/G]TCACATGCAGTCCTG | 11137 |
rs566012865 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684268 | TGGGGAAGCAAAACC[A/T]GCATCCTATTTATGA | 11137 |
rs566098397 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683878 | CCTTGTAATCCAACT[A/G]CCTCGGCCTCCCAAA | 11137 |
rs566132056 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696180 | TGGGACTACAGGCAC[A/G]TACCACCACACCCAG | 11137 |
rs566218039 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693339 | TTTTTCATAGGGGTG[-/T]TTTTTTTTTGTTTTT | 11137 |
rs566346040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690018 | CACTGAGCAGGTTAA[A/G]TAAGTTATTTACTTA | 11137 |
rs566426707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107690672 | TTCACCATGTTGGCC[A/G]GGATGGTCTCAATCT | 11137 |
rs566435538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696723 | TATTTTATGAAGTTA[C/T]AGAGTTCTTAACACA | 11137 |
rs566612754 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704869 | AAGTATTTGGGTTTA[C/G]GGTTGAAAGCATAAG | 11137 |
rs566686574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702769 | ATACTCTTGTTTCCT[C/T]TCATAATCTTCGGTA | 11137 |
rs566686611 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant | PWP1 | GRCh38.p7 | 12:107709252 | GAATCTCCCTGGGTA[C/T]CTGTTTTTTATTTAT | 11137 |
rs566953379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695052 | CGAGTTCAGGAGATC[A/G]AGACCATCCTGGCTA | 11137 |
rs567043344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701812 | CCTCCTGAGTAGCTG[A/G]GATTACTGGTGCATG | 11137 |
rs567071189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687988 | GTGAGCCGAGATGGC[A/G]CCATTGCTCTTCAGC | 11137 |
rs567141677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694349 | CTGATAAGTCCTTTT[C/G]TTATAGGAAACACAG | 11137 |
rs567182142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701305 | GCCTCCCTTTGCCTG[C/T]TTTTTGTGTTTGATG | 11137 |
rs567244263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690756 | GGGAGAGTCGAAAAT[G/T]ACATTGAGGAAATAG | 11137 |
rs567266116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691417 | TAAAGGTTTTTGAGC[A/G]TGGAACACATAATAA | 11137 |
rs567328307 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705988 | TACTGTCTTCCACAA[C/T]GGTTGAACTAGTTTA | 11137 |
rs567402010 | snp | G/T | 1.7821e-05 | 0.00298499 | intron-variant | PWP1 | GRCh38.p7 | 12:107697643 | ATGACAGAGGTAAGT[G/T]TACTCGGGAGTAGGG | 11137 |
rs567488371 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PWP1 | GRCh38.p7 | 12:107696900 | CCTGATATGTGAGAT[A/G]TTACCAGCTAGAGTT | 11137 |
rs567495450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709326 | TTTTCTGTTGGAACT[A/G]TTGCATTAACAAATA | 11137 |
rs567527116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703497 | CTACATTTTCTTTAA[C/G]TGCCAGCCTTTATGT | 11137 |
rs567619149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695893 | TTCTATGAATGACCT[A/G]GAAGACAGGACCATT | 11137 |
rs567634407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708825 | TTTTCATAAGTTCCA[C/T]CAGTAAGTCATATAG | 11137 |
rs567655389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695103 | TACTAAAAATACAAA[A/C]AAAAAAAAAAAAATC | 11137 |
rs567738381 | in-del | -/AGC | 0.000230909 | 0.0107425 | cds-indel | PWP1 | GRCh38.p7 | 12:107709122 | TTAGGTCTTGATCTT[-/AGC]AGTCAAATCAAGGGC | 11137 |
rs567741234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701968 | TAGGCATGAGCCACC[A/G]CGCCCAGCCCCATTT | 11137 |
rs567775452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689334 | TAGGAAAAACATAAT[A/G]TATATAAGGTTTGGT | 11137 |
rs568061130 | snp | A/C | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712924 | ATTGTCTTCCTATTA[A/C]GTATGAGTTTTAGTA | 11137 |
rs568194051 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PWP1 | GRCh38.p7 | 12:107707063 | CATTTGTTTGTGTCC[C/T]CTTTTATTTCGTTGA | 11137 |
rs568451823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687341 | ATTAAAAAGAGACAT[A/G]TAGCCTTTCAAATAC | 11137 |
rs568480059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689558 | CGAGACCAGCCGGGC[C/G]AACATGGCGAAACCC | 11137 |
rs568480332 | snp | C/T | 6.63559e-05 | 0.00575965 | intron-variant | PWP1 | GRCh38.p7 | 12:107696627 | TGATTTCCAGTCTTA[C/T]GTATTTTCTCCTAGC | 11137 |
rs568497835 | snp | C/T | 0.00102217 | 0.0225841 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693074 | CCGAGCTGAACAGGA[C/T]CAGTGCAATTTAGAG | 11137 |
rs568537754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693585 | ATATAAAAATACAAG[C/G]CTGGGTGCGGTGTCT | 11137 |
rs568695221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706216 | GAGAAGTGTCTATTC[A/G]TATCCTTCGCCCACT | 11137 |
rs568853261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107702669 | GTAGATCAGTTTATA[A/G]CTCCATCTGTAGATG | 11137 |
rs568862294 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PWP1 | GRCh38.p7 | 12:107707883 | CGTTGTGTCTCTGCC[A/G]GGCTTTGGTATCAGG | 11137 |
rs568892298 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686298 | CAAAAGGCTTTTTGA[C/T]AACACCACTAGCTTC | 11137 |
rs568964355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702163 | TGATGCCAGGAAATA[C/T]GAACTTGCCAACTTT | 11137 |
rs569174043 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | PWP1 | GRCh38.p7 | 12:107709840 | ACAGAAGCAATTTTT[-/G]TAGTACCATCTCATG | 11137 |
rs569329986 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712674 | TCCTAACTGTTCTCA[A/G]ATTAATGCTCATGAT | 11137 |
rs569525494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700619 | TGGATACTGTGAATA[A/C]TGCTGCTATGAATGT | 11137 |
rs569564253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706280 | TTTGAGTTCATTGTA[C/G]ATTCTGGATATTAGC | 11137 |
rs569736427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699213 | GCAGTGAGCTGAGAT[C/T]GTGCAACTGCACTCT | 11137 |
rs569772729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107698695 | GCTCAAGAGATCCTG[C/G]GATTCTCCTGCCTCA | 11137 |
rs569813630 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700976 | CTCAAGCAATCCCCC[C/T]GCCTCAGCTTCCCAA | 11137 |
rs569849940 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686105 | GAGGGCGGCTTTGCC[C/T]GGATTGTCGCGACTA | 11137 |
rs569895521 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692088 | AACAAATAACCCAGC[C/T]TGGAGAGATGGCATT | 11137 |
rs569982737 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712552 | AAAGCGTAAAATCCG[A/G]TAATATTAAAAGATA | 11137 |
rs570174780 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107711289 | TTGGGCAGGCCAGGC[A/G]TTCCTTGCCCTCATT | 11137 |
rs570482187 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107686694 | AAGTCCCGCCGGGCG[C/T]GGTGGCTCACGCCTG | 11137 |
rs570697127 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689618 | AGGCGTGGTGGCGCA[A/C]ATCTGTAATCCCAGC | 11137 |
rs570803968 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686793 | AACACGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 11137 |
rs570811911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704958 | ATTTTGCTGGTTGCC[A/G]GCCATTCCAAAGTGT | 11137 |
rs570915906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699949 | TGGCTGGGGAGGCCT[C/G]ACAGTTATGGCAGAA | 11137 |
rs570972422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705292 | GAAAAGCCCAGCTTT[C/T]ATCCAGAGCAAAGAT | 11137 |
rs571057902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687774 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 11137 |
rs571118746 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107711396 | GGCCAGATTTTGGGG[C/G]GCTTGTTCCCAGCAA | 11137 |
rs571244122 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704429 | AAACCACTGTAACGT[C/T]AGAGGCACCAGTGCC | 11137 |
rs571361126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709387 | TAGTCAAATTTGGTG[A/G]GATTTTATGACTTAG | 11137 |
rs571444135 | snp | C/T | 0.000164379 | 0.00906435 | intron-variant | PWP1 | GRCh38.p7 | 12:107697772 | TCCAAAGAAAACTTA[C/T]TTCTGATTACATAAA | 11137 |
rs571776404 | in-del | -/CTCACT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698095 | AGGCCACGCACGTGG[-/CTCACT]CCTGTAATCCCAGCA | 11137 |
rs571787698 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683833 | AGACGGGGTTTCACT[A/G]CGTTGGCCAGGCTTG | 11137 |
rs571813290 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694670 | TTCTAATTTCAAAAA[A/C]TTGAGAACCTATTAG | 11137 |
rs572054898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710346 | AGACAACAGTGAGGA[G/T]CTAGATATTAGCGCT | 11137 |
rs572079281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710986 | AAAGACACACACACA[C/G]AAATATAGAGATGTG | 11137 |
rs572253418 | snp | A/G | 3.2994e-05 | 0.00406152 | intron-variant | PWP1 | GRCh38.p7 | 12:107703637 | GTTAGGTAATTTTAC[A/G]AAAAGCAAACCAACA | 11137 |
rs572290309 | snp | A/G | 1.65732e-05 | 0.00287859 | intron-variant | PWP1 | GRCh38.p7 | 12:107703066 | CACAGCGGTTCTTAA[A/G]AATCGGACACAAATA | 11137 |
rs572292140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709484 | GGCTGGGGAGAGGGT[G/T]TTCTAGGACACAAGT | 11137 |
rs572340888 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107690953 | GAATAGGACATGAGA[C/T]ATGGTCTGTGTTGGG | 11137 |
rs572366872 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684808 | TGCAAAAAGGTCCCC[A/G]AATAGAGCCCACAGG | 11137 |
rs572372649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690505 | GTCTTGCTCTGTTGC[C/T]CAGGCTAGAGTGCTG | 11137 |
rs572426452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697848 | GCTAGTATATTAATA[C/T]GAATAGCTACTATAG | 11137 |
rs572590540 | in-del | -/TC | 0.000198249 | 0.00995415 | intron-variant | PWP1 | GRCh38.p7 | 12:107710394 | TCACCATCTTCCTGT[-/TC]TCTCTCTAGGGAGTT | 11137 |
rs572636804 | snp | A/G | 1.65927e-05 | 0.00288029 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688737 | ACCCAGAGGATGACA[A/G]GACGCTTGATGATGA | 11137 |
rs572653182 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690378 | CCATGTCTAAATAAT[-/A]AAAAAAGTTTAAAAA | 11137 |
rs572885906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689575 | ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA | 11137 |
rs573136432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107702185 | GCCAACTTTGTTCTT[C/T]TTTTCAGTACTATTT | 11137 |
rs573224321 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708131 | GTGTTGTACTTCGGC[G/T]CTCACTCTTCAGGTA | 11137 |
rs573485604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693931 | TCTTCCTAATAATTC[A/G]ACACAAAGGGCCACG | 11137 |
rs573607067 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PWP1 | GRCh38.p7 | 12:107686838 | GGGTGTGGTGGTGGA[C/T]GCCTGTAGTCCCAGC | 11137 |
rs573679998 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683889 | AACTGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 11137 |
rs573774573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689602 | AATACAAAACTTAGC[C/T]AGGCGTGGTGGCGCA | 11137 |
rs573837729 | snp | A/G | 0.000185399 | 0.00962626 | intron-variant | PWP1 | GRCh38.p7 | 12:107688838 | TGGTTTGTAATTACA[A/G]GCTCAATATGTTGGA | 11137 |
rs573865603 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703518 | GCCTTTATGTGGGAG[C/T]ATGGTTTGCCCTTTG | 11137 |
rs573866671 | in-del | -/AGTA | 0.000676211 | 0.0183752 | intron-variant | PWP1 | GRCh38.p7 | 12:107692899 | TACTCTGAAAGATAC[-/AGTA]AGTATTTACATCTTT | 11137 |
rs574020904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708196 | CATATATATTAGAAT[C/T]CCAAATATTTAGGGA | 11137 |
rs574086804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107707610 | TTTAGCATGAAGGGC[G/T]GTTGAATTTTGTCAA | 11137 |
rs574154190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694281 | CGATACTCTCCTCCC[A/C]CAGCAGTCTTCAGAT | 11137 |
rs574275694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706574 | CTGGAATTAATTTTT[C/G]TATAAGCTGTGAGGA | 11137 |
rs574277498 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700495 | TTCAGTCATGTTCCA[A/G/T]TAAGTGTCAGAGTTT | 11137 |
rs574361835 | snp | C/T | 0.175576 | 0.238665 | intron-variant | PWP1 | GRCh38.p7 | 12:107705860 | GCACATATGCACATA[C/T]GTGTGCATGTGTCTT | 11137 |
rs574393190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107687556 | AAGAGTTTATAGGAA[A/G]AAGAGATTGAATTTA | 11137 |
rs574612618 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712832 | GCCATTCTGTGCCTA[A/G]TGCTATACAAGGCAT | 11137 |
rs574680426 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712471 | TTTTAAAAAGTAATT[C/T]CTTAAACATACCATC | 11137 |
rs574909497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686193 | TCTCACTGTTCCCAC[A/C]CTCAAGCCCAACCCC | 11137 |
rs574985872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695221 | CAGTGGGCTGAGATC[A/G]TGTCACTGCACTCCA | 11137 |
rs574987695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107688258 | TGAAGTTTCAGGTAG[C/T]GAGAGATCTTATTTG | 11137 |
rs575001387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692429 | CCCTTATTTATTATG[C/T]TGATTTCAGTGTTTC | 11137 |
rs575027528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694859 | TTGGGTTTGGAAGGA[A/T]TCTCCAAATTGCCCA | 11137 |
rs575145982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699280 | AAACAAAACAAAATA[A/G]TCTTAAGGTTTAAAG | 11137 |
rs575258188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107705361 | GTAGTGCTTTGCAAA[A/G]GTGAGAAAGAGTTTT | 11137 |
rs575260109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698879 | ATTACAGTGTGGGCC[A/G]CTGCACCCAGCCCCT | 11137 |
rs575364719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701520 | ATCGCTTAAGTCAGG[A/G]TCATGAAGGTTTACA | 11137 |
rs575694003 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712885 | CTTTGCTCTCCACCT[A/G]ACAAGGGACAGTTTT | 11137 |
rs575780929 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712505 | CACAGTTAATCTAGA[C/T]TTGTAAATAGGTAGT | 11137 |
rs575838472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686234 | TCGCACGCACATGGA[C/T]TTAGCGGGCCGGAAA | 11137 |
rs575966597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705707 | AGGACATGAACTCAT[C/T]CTTTTTTATGGCTGC | 11137 |
rs576001495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693177 | CCATTTCATTTTTAG[A/G]TGCCAGATCCTATTG | 11137 |
rs576036054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107692507 | TTCAATCATGAATGC[A/G]GGGAGCTAGCTAGAG | 11137 |
rs576065888 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690584 | TTTTCCTGCCTTAGC[C/T]TCCCGAATGCTGGGA | 11137 |
rs576087453 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107691252 | CCCAAAGGAGGGGAA[A/G]TGCTCGGCAAGTTGA | 11137 |
rs576097725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107705032 | GTTTGAAATACTAAG[C/T]ATAGTTAGTATTTTT | 11137 |
rs576174478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697903 | CTCCTCCAAATACAG[C/T]AGCTATTTATACAGA | 11137 |
rs576245975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697256 | AGCAGCAGCACAGCA[C/T]GGTTATCACCTGTGA | 11137 |
rs576320675 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685640 | AAAGCCTTTTCTCTA[C/T]ACTTCACACAGCCCA | 11137 |
rs576380541 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684923 | ACCTTCCTGTTTCTT[C/T]TGCTTGCCTCTCTCA | 11137 |
rs576509313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107687043 | CGACATGTGCACATA[C/T]AGTATGTCAGTGGGA | 11137 |
rs576567443 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PWP1 | GRCh38.p7 | 12:107705764 | ACATTTTCTTAATCC[A/C]GTCTATCATTGATGG | 11137 |
rs576614517 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107705450 | TATGTATACATGTGC[C/G]ATGTTGGTGTGCTGC | 11137 |
rs576615187 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | PWP1 | GRCh38.p7 | 12:107703760 | AAGTAAGAAAGCACA[A/G]CAAGAATGATTGCTA | 11137 |
rs576645052 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107710151 | GTGATAACGAAGATG[A/C]GTGGCCTGAGTGGTC | 11137 |
rs576756326 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687564 | ATAGGAAAAAGAGAT[G/T]GAATTTATGAAATCC | 11137 |
rs576775527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700789 | TACATTTTCACCAAC[A/G]ATGCACACAAGGGCT | 11137 |
rs576833018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686149 | GAAGGTCTGGTTCGC[C/T]TGAGCCTGGAGAGTC | 11137 |
rs576919449 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685776 | TGCCCAAACAGGAGC[C/T]TGCGCATGCGCTCTG | 11137 |
rs577104364 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698034 | GGGTTGGGAGCTATA[C/T]TGATACTTGTATAAT | 11137 |
rs577358026 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708519 | CTCTGCCACACTGGT[C/T]GATTTGACTGTTGGT | 11137 |
rs577416899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107698193 | ATGGTGAAACCCTGT[C/T]TCTACTAAATATACA | 11137 |
rs577420175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704891 | AAGCATAAGGTGTTT[G/T]TTTTTAAATAAGAGA | 11137 |
rs577505386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107704305 | GCCTAAGACATGAGT[A/G]ACCTGGCTCTGAGCT | 11137 |
rs577650439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710932 | AGGCCGAGACCAGCT[C/T]GGTTGGGGAGACCCT | 11137 |
rs577688908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107710206 | AGAACCAGCATGCTG[C/T]GCTTGTCTGGCTTCA | 11137 |
rs577744941 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698830 | ACTCCCGGCCTCAAG[C/T]GATGTTCCCACGTTA | 11137 |
rs577755875 | snp | A/G | 0.000399281 | 0.0141238 | missense | PWP1 | GRCh38.p7 | 12:107708966 | ATAATTTGGATGCAC[A/G]TTCAGATAAGCCAAT | 11137 |
rs577875971 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684458 | CATCCTTGAAAAATA[G/T]TATCTGCCATATGGT | 11137 |
rs577897727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697067 | AAGGTAAACACTGTT[C/T]ATACTGTCTTACGTC | 11137 |
rs577912896 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684032 | TTGCCTTCTGCAGTG[A/G]TTGTGAGGCTTCCCC | 11137 |
rs577971512 | snp | C/T | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107696324 | AGGCACGAGCCACTG[C/T]GCCCAGCCTGGAATC | 11137 |
rs578018187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689609 | AACTTAGCCAGGCGT[A/G]GTGGCGCACATCTGT | 11137 |
rs578107117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708286 | GCCAAGCCTTCTCTT[C/T]CCTGGCCTAGCAGTC | 11137 |
rs745376936 | snp | A/C/T | 4.96761e-05 | 0.00498357 | intron-variant | PWP1 | GRCh38.p7 | 12:107703056 | TTTAGTTGATCACAG[A/C/T]GGTTCTTAAAAATCG | 11137 |
rs745426332 | in-del | -/G | 6.59729e-05 | 0.005743 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107709232 | TAGGGACATGAAAAT[-/G]GTAAGAATCTCCCTG | 11137 |
rs745563164 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711664 | AGAGATAATATATAT[A/G]TCTCCCCACTGTATG | 11137 |
rs745574499 | snp | A/G | 4.0971e-05 | 0.00452591 | splice-donor-variant | PWP1 | GRCh38.p7 | 12:107688803 | AGGAAGGTGACCCAG[A/G]TTAGTTTATCCACTT | 11137 |
rs745576577 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107703699 | GGTCCAAACACTGCA[A/G]TTTCATCCATTTGAA | 11137 |
rs745625736 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692125 | CAGCTCTTTCTCGTG[C/T]AGCAGAAATTGCTTT | 11137 |
rs745641774 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704100 | CTCATATCAGTGCTC[C/T]TTTTTACAGATTGGG | 11137 |
rs745665762 | snp | G/T | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696511 | TTTTTATGTACACCA[G/T]GATATACTCTTGTCT | 11137 |
rs745776391 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | PWP1 | GRCh38.p7 | 12:107712165 | GGAGTGCAAGAAATT[C/T]ATCTATTAGTGGCCC | 11137 |
rs745872628 | snp | A/G | 1.75093e-05 | 0.00295877 | intron-variant | PWP1 | GRCh38.p7 | 12:107697422 | GATTAGAAGTTCTGT[A/G]TGTCTTTTTTTGTGT | 11137 |
rs745908678 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699030 | ACACTTTGGGAGGCC[A/G]AGAGTGGATCATGAG | 11137 |
rs745952551 | snp | C/G | 1.6966e-05 | 0.00291251 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686019 | AGCGTCTTTACGGCA[C/G]TGGGGGTCCGCCCAG | 11137 |
rs745978102 | snp | A/T | 0.000180067 | 0.00948688 | intron-variant | PWP1 | GRCh38.p7 | 12:107697824 | TTTCTTACACAAAAC[A/T]AGTTCAAAGCTAGTA | 11137 |
rs746168875 | snp | C/G/T | 3.29882e-05 | 0.00406118 | intron-variant | PWP1 | GRCh38.p7 | 12:107688567 | CATGTGGTCTTGTTA[C/G/T]TAGAAGGTAGCATTT | 11137 |
rs746321176 | snp | A/G | 8.46805e-05 | 0.00650639 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697591 | GAAGAAAAAGAAAGG[A/G]AAGAAGGTAAAGAAG | 11137 |
rs746424861 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | PWP1 | GRCh38.p7 | 12:107709230 | TCTAGGGACATGAAA[A/G]TGGTAAGAATCTCCC | 11137 |
rs746471222 | in-del | -/T | 1.65018e-05 | 0.00287239 | intron-variant | PWP1 | GRCh38.p7 | 12:107712095 | TTAGTTTCTTACCTG[-/T]TTATTTGTATTTTAG | 11137 |
rs746500767 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696131 | TCCACCTCCCAGGTT[A/C]AAGCTATTCTCCTGC | 11137 |
rs746501244 | snp | A/T | 1.65266e-05 | 0.00287455 | intron-variant | PWP1 | GRCh38.p7 | 12:107704625 | CCCTAACTTTGCCTG[A/T]ATGTGTCTAGGTCAG | 11137 |
rs746520266 | in-del | -/AAAAAAAAAAAAAAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686970 | GTGAGACTCCGTCTC[-/AAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAATAGAA | 11137 |
rs746530850 | snp | A/T | 1.65012e-05 | 0.00287234 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692836 | GACTCTTGGTGAATC[A/T]CTCTTGGGTCTTACG | 11137 |
rs746588613 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694781 | GAGGAGCTGAGAAAG[A/C]AGTTAAAGCTGTTAT | 11137 |
rs746596993 | snp | C/T | 6.6107e-05 | 0.00574884 | intron-variant | PWP1 | GRCh38.p7 | 12:107709245 | ATGGTAAGAATCTCC[C/T]TGGGTATCTGTTTTT | 11137 |
rs746598297 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708741 | ATCCAGTAGACATGT[C/T]AACTGAATTAGCCCA | 11137 |
rs746694995 | snp | A/G | 1.65611e-05 | 0.00287755 | intron-variant | PWP1 | GRCh38.p7 | 12:107692939 | ATTATGCTCTTAAGT[A/G]TTCAAAAAACCTTAC | 11137 |
rs746732865 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707607 | AGTTTTAGCATGAAG[G/T]GCTGTTGAATTTTGT | 11137 |
rs746771109 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701970 | GGCATGAGCCACCGC[A/G]CCCAGCCCCATTTGT | 11137 |
rs746860135 | in-del | -/CT | 1.64933e-05 | 0.00287165 | intron-variant | PWP1 | GRCh38.p7 | 12:107703776 | CAAGAATGATTGCTA[-/CT]CTGTTTTTATCCTCT | 11137 |
rs746977496 | in-del | -/AG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694684 | AATTGAGAACCTATT[-/AG]AGTTTTTTTTGTCAT | 11137 |
rs746980455 | in-del | -/TATTC | 3.31186e-05 | 0.00406918 | intron-variant | PWP1 | GRCh38.p7 | 12:107709265 | TATCTGTTTTTTATT[-/TATTC]TGTTTCTGACCTTGT | 11137 |
rs747030058 | snp | A/C | 1.66001e-05 | 0.00288094 | upstream-variant-2KB, utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107685955 | GCTGCGGCGTGGCCA[A/C]AGAGACACCAGACAA | 11137 |
rs747065182 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691831 | CTGTCCTATGGATTA[C/T]TATTAACTTCATTTT | 11137 |
rs747106880 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702869 | TATTGTAAATGCAAT[C/G]CTTTTCTCATATTTA | 11137 |
rs747218002 | snp | A/G | 3.34342e-05 | 0.00408852 | intron-variant | PWP1 | GRCh38.p7 | 12:107693108 | CATGGTAAGTGATAA[A/G]TCCCTTATTAAAAGA | 11137 |
rs747485683 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | PWP1 | GRCh38.p7 | 12:107688575 | CTTGTTATTAGAAGG[C/T]AGCATTTGGGTGATT | 11137 |
rs747495210 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711015 | TGAAGTGGGAAATCA[A/G]GGGTCTCACAGCCTT | 11137 |
rs747575766 | snp | A/G | 1.68004e-05 | 0.00289826 | intron-variant | PWP1 | GRCh38.p7 | 12:107699324 | AATATATTCAGTTTT[A/G]TTATGAGGGGGACTT | 11137 |
rs747623244 | snp | C/T | 3.29679e-05 | 0.00405991 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693065 | AGTTTGTGGCCGAGC[C/T]GAACAGGACCAGTGC | 11137 |
rs747628607 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705296 | AGCCCAGCTTTCATC[C/T]AGAGCAAAGATTAGT | 11137 |
rs747659301 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690927 | AGAGCAGTGTAGTTG[A/G]AGTGTGGAAAGAATA | 11137 |
rs747702379 | snp | C/G | 1.65386e-05 | 0.00287559 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699378 | ATTATTACAGAGTTC[C/G]TCAGCAGAAGGGCAT | 11137 |
rs747713924 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704449 | GCACCAGTGCCTTCA[A/G]GTGTTAAGATCAGAA | 11137 |
rs747764091 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686316 | CACCACTAGCTTCAC[C/T]AGCACCCAAGTGCAT | 11137 |
rs747799425 | snp | C/T | 0.000609216 | 0.0174426 | intron-variant | PWP1 | GRCh38.p7 | 12:107710538 | AGTTCTCTGCACACC[C/T]CCCCCTGCCCCTGTA | 11137 |
rs747940137 | in-del | -/T | 1.64776e-05 | 0.00287028 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107712201 | CAGCAGGAGCTCAGA[-/T]TACACCCATGGAGTC | 11137 |
rs747945603 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695812 | TATAATCAGCTAGAC[C/T]ATTAAAAGATAAAAT | 11137 |
rs747963675 | in-del | -/TTCG | 1.64838e-05 | 0.00287083 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107710477 | GTCAAAAAGAAGGGC[-/TTCG]TTCGGGTCTGGGATA | 11137 |
rs748033317 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694548 | TTGTGATCTGTTTAT[G/T]CATAGCAGGCACTTT | 11137 |
rs748037554 | snp | C/T | 4.94841e-05 | 0.00497389 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704723 | GAGAGTGACTTGGAA[C/T]CACTTTTCACCTTGT | 11137 |
rs748131399 | snp | C/T | 1.65173e-05 | 0.00287374 | intron-variant | PWP1 | GRCh38.p7 | 12:107704631 | CTTTGCCTGAATGTG[C/T]CTAGGTCAGTGGCTT | 11137 |
rs748230828 | snp | C/T | 1.65375e-05 | 0.0028755 | missense | PWP1 | GRCh38.p7 | 12:107708965 | TATAATTTGGATGCA[C/T]GTTCAGATAAGCCAA | 11137 |
rs748244591 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701905 | CTTGTCTCAAACTCC[A/G]GACCTCAAGTGATCT | 11137 |
rs748276050 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707925 | CTCATAAAATGAGTT[-/A]GGGGGGAAAGAGTTT | 11137 |
rs748343531 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701262 | CCTCCCAAAGTGCTG[C/G]GATAACAGGCATGAG | 11137 |
rs748426966 | snp | A/C | 3.30344e-05 | 0.004064 | intron-variant | PWP1 | GRCh38.p7 | 12:107709065 | AACTTATGATGAAGT[A/C]AATCTGTATTTCAAA | 11137 |
rs748427071 | snp | A/T | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696535 | CTTGTCTGCATATCC[A/T]CTGAGTGTGGAATGG | 11137 |
rs748467153 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709871 | CTTATTTTTAAGTGC[A/T]TAATTGCCTAAATGC | 11137 |
rs748492230 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697447 | TTGTGTAATCATACA[G/T]GCATTGTTTCCTCCC | 11137 |
rs748549929 | snp | A/G | 1.65457e-05 | 0.00287621 | intron-variant | PWP1 | GRCh38.p7 | 12:107702900 | ATGCTCTTGACTTTT[A/G]AAAGATTACCTGATT | 11137 |
rs748622210 | snp | C/T | 1.82151e-05 | 0.00301782 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688783 | CGACTTAGATAAATA[C/T]GATGAGGAAGGTGAC | 11137 |
rs748712055 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688695 | CACGCACCCAGGCAC[A/G]CCCAAGAGAGCCCCT | 11137 |
rs748794899 | snp | A/C | 1.68312e-05 | 0.00290092 | intron-variant | PWP1 | GRCh38.p7 | 12:107710542 | CTCTGCACACCTCCC[A/C]CTGCCCCTGTAAAAA | 11137 |
rs748988886 | snp | C/T | 8.23744e-05 | 0.0064172 | missense | PWP1 | GRCh38.p7 | 12:107712146 | CGAGAGAGGCTTGTT[C/T]TTGGGAGTGCAAGAA | 11137 |
rs748997227 | snp | C/G | 1.64933e-05 | 0.00287165 | intron-variant | PWP1 | GRCh38.p7 | 12:107702930 | TGGATTCTTCCCTTT[C/G]TCAGAAATGTTTTAG | 11137 |
rs749041878 | snp | G/T | 1.65072e-05 | 0.00287286 | missense | PWP1 | GRCh38.p7 | 12:107704742 | TTTTCACCTTGTCAT[G/T]TCTTGGTAAGAGTAC | 11137 |
rs749084645 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694308 | AGATCGTCTTGAAAC[A/T]TTGAAGATTCGAAGA | 11137 |
rs749100196 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693537 | TTCACTCCTCTCCTA[C/T]TCCTGCTATAAAAAA | 11137 |
rs749276199 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703191 | CACAAAGCCCTGTGT[A/G]GTAGGTATAATGCCC | 11137 |
rs749330151 | snp | A/G | 1.70403e-05 | 0.00291888 | intron-variant | PWP1 | GRCh38.p7 | 12:107697463 | GCATTGTTTCCTCCC[A/G]TAGGAAATTACATTG | 11137 |
rs749332264 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701001 | TCCCAAGTCACTTGG[A/G]GTACAGGGGCTTGCC | 11137 |
rs749457374 | snp | A/T | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712354 | ACATTCCTTTCTGCA[A/T]CTGCGGTGGCACCAC | 11137 |
rs749576800 | snp | C/T | 1.66272e-05 | 0.00288328 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685849 | AGTGCGGTCGTGGTC[C/T]CTCCCTATGCAGCCT | 11137 |
rs749581735 | snp | G/T | 1.6557e-05 | 0.00287719 | missense | PWP1 | GRCh38.p7 | 12:107697560 | TCTTCACACTCGGAA[G/T]TAAACTTTCAAAAAA | 11137 |
rs749654705 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690166 | CTTAATACAAATGTT[A/G]TCTGCAACAAAGTAA | 11137 |
rs749678889 | snp | A/G | 1.88581e-05 | 0.00307062 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688790 | GATAAATATGATGAG[A/G]AAGGTGACCCAGGTT | 11137 |
rs749828566 | snp | C/T | 1.70281e-05 | 0.00291783 | intron-variant | PWP1 | GRCh38.p7 | 12:107692786 | AGATGACTATTTTAT[C/T]ATTGTAGTTTGTCAA | 11137 |
rs749879560 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698462 | GCCCAGGAGGTTGAG[A/G]TTGCAGTGAGCCATG | 11137 |
rs749922675 | snp | C/G | 8.30089e-05 | 0.00644186 | upstream-variant-2KB, utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107685907 | TGAGGACCATGAACC[C/G]CAGCCGCCAGGTGAC | 11137 |
rs749968462 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | PWP1 | GRCh38.p7 | 12:107697653 | TAAGTTTACTCGGGA[A/G]TAGGGGTGAAGGGTA | 11137 |
rs750019297 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710657 | CCTTCTGTATAGCTG[A/G]GATTACAGGTGTGAG | 11137 |
rs750102470 | in-del | -/GTTA | 3.30557e-05 | 0.00406531 | intron-variant | PWP1 | GRCh38.p7 | 12:107712079 | TTAATTTCCTGATCT[-/GTTA]GTTTCTTACCTGTTT | 11137 |
rs750242818 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685817 | GGCCCTGTGCAGATC[C/T]CTGAGCGTGTGGCAG | 11137 |
rs750294298 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697531 | CCTTGATATAGTGGA[C/T]TCTTTAGAGCCAGTC | 11137 |
rs750334462 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699593 | GCTCTGTCATCTGTT[C/T]CTTTGCATCCTCCAG | 11137 |
rs750463029 | in-del | -/AAAAG | 0.000177289 | 0.00941346 | intron-variant | PWP1 | GRCh38.p7 | 12:107697821 | TCTTTCTTACACAAA[-/AAAAG]ACTAGTTCAAAGCTA | 11137 |
rs750477747 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706467 | GACATGAAGTCCTTG[C/T]CCATGCCTATGTCCT | 11137 |
rs750502852 | snp | C/G | 1.65031e-05 | 0.00287251 | missense | PWP1 | GRCh38.p7 | 12:107710510 | AGCACAGTCTCTTCA[C/G]GTAAGGATTTTTAGT | 11137 |
rs750519767 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708293 | CTTCTCTTCCCTGGC[C/T]TAGCAGTCAGACTGC | 11137 |
rs750534514 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694246 | CTGCGCTCATATCCT[C/T]AGACAAGTCCATCCT | 11137 |
rs750559214 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705141 | TGAGAATGCTAACCT[A/G]TTAATTTGTAGCACT | 11137 |
rs750594287 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685518 | AAGTCTACGGAACTG[A/C]AAGCAAAATAAAGAT | 11137 |
rs750625437 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | PWP1 | GRCh38.p7 | 12:107702964 | GTGCATCAGCTGACA[A/G]CACTGTAATTCTGTG | 11137 |
rs750680842 | snp | A/G | 1.65556e-05 | 0.00287707 | intron-variant | PWP1 | GRCh38.p7 | 12:107699450 | GTAAAAAGAAATAAC[A/G]TTTGAATGATTGTAA | 11137 |
rs750698291 | snp | A/T | 1.6517e-05 | 0.00287372 | intron-variant | PWP1 | GRCh38.p7 | 12:107712084 | TTCCTGATCTGTTAG[A/T]TTCTTACCTGTTTAT | 11137 |
rs750725194 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696072 | GAGTCTCACTATGTC[A/G]CCCAGGCTGGAGTGC | 11137 |
rs750762832 | snp | A/G | 3.29837e-05 | 0.00406088 | missense | PWP1 | GRCh38.p7 | 12:107704684 | TGAAAGCCATCGAAT[A/G]TGGCGATTCAGTGGG | 11137 |
rs750842913 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | PWP1 | GRCh38.p7 | 12:107692902 | TCTGAAAGATACAGT[A/G]AGTATTTACATCTTT | 11137 |
rs750916283 | in-del | -/TGA | 3.29783e-05 | 0.00406055 | cds-indel | PWP1 | GRCh38.p7 | 12:107688633 | AGAAGGTGGTGGCAG[-/TGA]TGAAGAGGAGACAGG | 11137 |
rs751014329 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709622 | TATCTCTTTGCATAA[C/G]TAGTTCTGACTACAC | 11137 |
rs751035596 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693006 | CTCACTTAGGAACAA[C/T]ATGAACGTGAAGATT | 11137 |
rs751041160 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691520 | GAGGAGCAGAAACTT[A/C]AGATAAATTAGGCCA | 11137 |
rs751083294 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709510 | AAGTGAAATGGCTGC[-/T]TTTTTTTTTTTTTTT | 11137 |
rs751110052 | snp | G/T | 1.64925e-05 | 0.00287158 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688622 | GCTCATAGAGAAGAA[G/T]GTGGTGGCAGTGATG | 11137 |
rs751186951 | in-del | -/TTGT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697082 | ATACTGTCTTACGTC[-/TTGT]TTGTTTGCACACCTT | 11137 |
rs751189731 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693056 | TAATCTTATAGTTTG[C/T]GGCCGAGCTGAACAG | 11137 |
rs751274825 | in-del | -/ATA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703931 | GAACATGATTCTGTC[-/ATA]ATAATATAACTGTAG | 11137 |
rs751281717 | snp | G/T | | | missense | PWP1 | GRCh38.p7 | 12:107704704 | GATTCAGTGGGCAGA[G/T]AGAGAGAGTGACTTG | 11137 |
rs751340623 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684824 | AATAGAGCCCACAGG[C/T]GGACACCCCCCGTTT | 11137 |
rs751371760 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698344 | CCTGTGTGACAGAGC[A/G]AGACTCTGTCTCAAG | 11137 |
rs751415192 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697157 | CATGAAGGAGGACGG[A/G]AGGAGGGTTATTCTC | 11137 |
rs751427418 | snp | C/T | 1.65559e-05 | 0.00287709 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688478 | GAAGAAGTAAAACGC[C/T]TCATTGCTGAGGCAA | 11137 |
rs751663905 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704856 | TTTTAACAGTATGAA[A/G]TATTTGGGTTTAGGG | 11137 |
rs751696349 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703938 | ATTCTGTCATAATAA[C/T]ATAACTGTAGGAACT | 11137 |
rs751758283 | snp | C/T | 1.65135e-05 | 0.00287341 | intron-variant | PWP1 | GRCh38.p7 | 12:107688849 | TACAAGCTCAATATG[C/T]TGGATCATGTTTGTG | 11137 |
rs751772588 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708819 | GTTAATTTTTCATAA[A/G]TTCCACCAGTAAGTC | 11137 |
rs751819394 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685766 | GCGCCGACGCTGCCC[A/T]AACAGGAGCCTGCGC | 11137 |
rs751842123 | snp | A/G | 1.70632e-05 | 0.00292084 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688763 | GATGATGAGCTGGCT[A/G]AGTACGACTTAGATA | 11137 |
rs751892446 | snp | C/T | 1.67713e-05 | 0.00289575 | intron-variant | PWP1 | GRCh38.p7 | 12:107696444 | TGACTCATTCTGATA[C/T]ATTAAAGTCTCTTTT | 11137 |
rs751932602 | snp | A/C | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712642 | AGAGGCAAGTGCCCC[A/C]GAGACTCCACTTTCA | 11137 |
rs751937492 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711755 | TGATGTGTGTGAGTC[C/G]TAAGTCCGAAAAGTT | 11137 |
rs751968290 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694184 | TTGCACAATGTCTGG[C/T]GCACTCTGCCTACAG | 11137 |
rs752010110 | in-del | -/GGGGG | 1.67826e-05 | 0.00289673 | intron-variant | PWP1 | GRCh38.p7 | 12:107699331 | TCAGTTTTATTATGA[-/GGGGG]ACTTTAATACAAAAA | 11137 |
rs752060483 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | PWP1 | GRCh38.p7 | 12:107712113 | ATTTGTATTTTAGTA[A/G]ATGAAGCATTTGGAA | 11137 |
rs752135129 | in-del | -/AAT | 1.65285e-05 | 0.00287471 | cds-indel | PWP1 | GRCh38.p7 | 12:107709001 | ACACTTAATGCACAC[-/AAT]GATGAAATCTCTGGT | 11137 |
rs752164567 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701506 | GTATCTAGCAAACCA[C/T]CGCTTAAGTCAGGGT | 11137 |
rs752216810 | snp | C/T | 1.70035e-05 | 0.00291572 | intron-variant | PWP1 | GRCh38.p7 | 12:107708897 | TTTTGTGACGTAGCA[C/T]GACCTTGCCCATCTT | 11137 |
rs752249668 | in-del | -/TGTTT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704839 | CTGAAAAGCTTTTTC[-/TGTTT]TAACAGTATGAAGTA | 11137 |
rs752251974 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689726 | ACTCCAGCCTGGGTG[A/C]CACAGTGGGACTCCA | 11137 |
rs752269987 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687921 | CTGTAATCCCAGCTG[C/T]TCAAGAGGCTAAGGC | 11137 |
rs752339670 | in-del | -/ATT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710054 | ATTTAAACTGGCATC[-/ATT]GTTATTGTTTAAAAG | 11137 |
rs752398438 | in-del | -/AT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711659 | ACACAGAGATAATAT[-/AT]ATATATCTCCCCACT | 11137 |
rs752414723 | snp | C/G | 3.30562e-05 | 0.00406534 | splice-donor-variant | PWP1 | GRCh38.p7 | 12:107709017 | ATGATGAAATCTCTG[C/G]TGAGCAAGAGTAATG | 11137 |
rs752414887 | snp | C/T | 1.65323e-05 | 0.00287505 | intron-variant | PWP1 | GRCh38.p7 | 12:107696469 | TCTTTTCCCAATCTT[C/T]TCAGTTTATAATCAA | 11137 |
rs752420849 | in-del | -/GGTGACGTGCGTGGCCTGGGTCCGCT | 1.65899e-05 | 0.00288005 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant | PWP1 | GRCh38.p7 | 12:107685917 | GAACCGCAGCCGCCA[-/GGTGACGTGCGTGGCCTGGGTCCGCT]GCGGCGTGGCCAAAG | 11137 |
rs752480182 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697080 | TTTATACTGTCTTAC[A/G]TCTTGTTTGCACACC | 11137 |
rs752496601 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709423 | TTTGTGGGGAATTCA[C/G]TGACTGGTTCTTTTC | 11137 |
rs752561403 | snp | A/T | 1.65222e-05 | 0.00287417 | missense | PWP1 | GRCh38.p7 | 12:107699418 | GTCCTTGACCTTTCA[A/T]GGAATAAGCTAATCA | 11137 |
rs752564787 | snp | A/G | 0.00011553 | 0.00759944 | intron-variant | PWP1 | GRCh38.p7 | 12:107688534 | CCAGATGAAATCTAT[A/G]TCTTAAATGATGATG | 11137 |
rs752582488 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708691 | TCTACTGCTCTAGCC[C/T]CATTCCAGACCATTC | 11137 |
rs752728105 | in-del | -/TAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697936 | ACCAACCTTGAACTT[-/TAA]TAAAAAAATTTCTGT | 11137 |
rs752742969 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | PWP1 | GRCh38.p7 | 12:107703787 | GCTACTCTGTTTTTA[C/T]CCTCTAGAAGTCATT | 11137 |
rs752761899 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698565 | TTCTTCCCTGTTCCT[C/T]GTAATGAAATTTTTT | 11137 |
rs752794889 | snp | A/G | 3.44145e-05 | 0.00414802 | intron-variant | PWP1 | GRCh38.p7 | 12:107692773 | TATGTTTTTGTCAAG[A/G]TGACTATTTTATTAT | 11137 |
rs752845865 | snp | C/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684131 | TTATTAGCAGTGTGA[C/G]AACAGACTACCACAG | 11137 |
rs752926149 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | PWP1 | GRCh38.p7 | 12:107709170 | TCAGCTGACAAATAC[A/G]TGAAGATCTGGGACA | 11137 |
rs753043911 | in-del | -/A | 4.95303e-05 | 0.00497621 | intron-variant | PWP1 | GRCh38.p7 | 12:107709083 | CTGTATTTCAAAGCG[-/A]AAAGTGTCTAAACTT | 11137 |
rs753253525 | in-del | -/TTCC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689305 | ATTATCATTATTTGA[-/TTCC]TAGGTACATATAGGA | 11137 |
rs753306460 | in-del | -/TGGGCTGC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686253 | CGGGCCGGAAAGGGG[-/TGGGCTGC]TGGGCTGCTGTTTTT | 11137 |
rs753372053 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | PWP1 | GRCh38.p7 | 12:107696622 | TTCAATGATTTCCAG[C/T]CTTATGTATTTTCTC | 11137 |
rs753404229 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699822 | TATGGCAAAATACAT[A/G]TAACATAAAAGTTAA | 11137 |
rs753478021 | snp | C/T | 1.6607e-05 | 0.00288153 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685879 | TGGTTTCTAGCGTGA[C/T]ACGCCCTTGACTTGA | 11137 |
rs753525689 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702342 | CTGGAGTCCAGTGAC[A/G]TGATCTTGGTTCTCT | 11137 |
rs753607444 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708537 | TTTGACTGTTGGTCA[C/G]GCCTTGGTTCCTTGA | 11137 |
rs753650086 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705195 | ATAAGACCTCTGTCT[-/A]AATACCCTTATTATC | 11137 |
rs753690607 | snp | A/G | 1.65272e-05 | 0.0028746 | intron-variant | PWP1 | GRCh38.p7 | 12:107709027 | CTCTGGTGAGCAAGA[A/G]TAATGCTTCTTTCAT | 11137 |
rs753730854 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705198 | AGACCTCTGTCTAAA[C/T]ACCCTTATTATCTAA | 11137 |
rs753852212 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703989 | GAGGCTGTACTTTGC[C/G]TTTATGGGAAGAATT | 11137 |
rs753871504 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687755 | TTAAAATTAAGGCCG[A/G]GCACGGTGGCTCACG | 11137 |
rs753897291 | snp | G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685682 | GTGGATTCCTCGCCC[G/T]GCTGCTTCCGCTTCC | 11137 |
rs753988444 | in-del | -/AATA | 1.72457e-05 | 0.00293642 | intron-variant | PWP1 | GRCh38.p7 | 12:107697609 | GAAGGTAAAGAAGTT[-/AATA]AATATTTAAACTCTA | 11137 |
rs754018834 | in-del | -/AAG | 6.65901e-05 | 0.0057698 | cds-indel | PWP1 | GRCh38.p7 | 12:107688461 | AGGTAGAGCTGAGTA[-/AAG]AAGAAGTAAAACGCC | 11137 |
rs754066376 | snp | A/G | 1.65963e-05 | 0.0028806 | intron-variant | PWP1 | GRCh38.p7 | 12:107710369 | TTAGCGCTTTCTGAA[A/G]AGATTGAAATCACCA | 11137 |
rs754067824 | snp | A/C | 6.59761e-05 | 0.00574314 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710500 | CTGGGATATAAGCAC[A/C]GTCTCTTCAGGTAAG | 11137 |
rs754186059 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691623 | GCTGGGAGTTTAGCA[G/T]CATCCTAGTGGATGA | 11137 |
rs754204360 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702429 | GGGATTACAGGCATG[C/T]GCCACCATGCCCAGC | 11137 |
rs754294249 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701743 | GAGTGAGTGGTGTGA[A/T]CTCAGCTCACTGCAC | 11137 |
rs754348033 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692884 | TCAAGATCCTTACGT[C/T]ACTCTGAAAGATACA | 11137 |
rs754460018 | snp | A/T | 3.29826e-05 | 0.00406082 | missense | PWP1 | GRCh38.p7 | 12:107704711 | TGGGCAGATAGAGAG[A/T]GTGACTTGGAATCAC | 11137 |
rs754463694 | snp | A/C | 1.6507e-05 | 0.00287284 | intron-variant | PWP1 | GRCh38.p7 | 12:107703796 | TTTTTATCCTCTAGA[A/C]GTCATTTTAAGAGTA | 11137 |
rs754467819 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690439 | ATCTGTTAGAATATC[A/G]TTGAAATGCTGAGTA | 11137 |
rs754552298 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711762 | TGTGAGTCCTAAGTC[C/T]GAAAAGTTCTGTGCC | 11137 |
rs754588186 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686235 | CGCACGCACATGGAC[C/T]TAGCGGGCCGGAAAG | 11137 |
rs754599042 | snp | C/T | 1.67483e-05 | 0.00289377 | intron-variant | PWP1 | GRCh38.p7 | 12:107696446 | ACTCATTCTGATACA[C/T]TAAAGTCTCTTTTCC | 11137 |
rs754600049 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711675 | ATATATCTCCCCACT[A/G]TATGATTCCTGCATC | 11137 |
rs754674042 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699840 | ACATAAAAGTTAACA[A/C]TTGTATTAGTCTGTC | 11137 |
rs754692533 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698813 | GCCTGGGCTGGTCTC[A/G]AACTCCCGGCCTCAA | 11137 |
rs754767490 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694345 | TAGGCTGATAAGTCC[C/T]TTTGTTATAGGAAAC | 11137 |
rs754802951 | snp | C/G | 1.67242e-05 | 0.00289168 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107685992 | GCCTGGTCGCTGGGA[C/G]ACAAGGGGAGCAGCG | 11137 |
rs754804944 | snp | A/G | 4.06661e-05 | 0.00450904 | intron-variant | PWP1 | GRCh38.p7 | 12:107697735 | TATGAAATTATTGTA[A/G]TTTTTAGTTTTGAAA | 11137 |
rs754831783 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702412 | CAGCCTCCTGAGTAA[C/G]TGGGATTACAGGCAT | 11137 |
rs754929994 | in-del | -/T | 1.64798e-05 | 0.00287047 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107712122 | TTAGTAAATGAAGCA[-/T]TTGGAAGACGAGAGA | 11137 |
rs755003907 | snp | A/G | 6.60829e-05 | 0.00574779 | utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107688498 | TGCTGAGGCAAAGGA[A/G]AAATTGCAGTAAGTT | 11137 |
rs755033561 | snp | A/G | 3.46344e-05 | 0.00416125 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688769 | GAGCTGGCTGAGTAC[A/G]ACTTAGATAAATATG | 11137 |
rs755232176 | snp | C/G | 3.2722e-05 | 0.00404474 | intron-variant | PWP1 | GRCh38.p7 | 12:107688852 | AAGCTCAATATGTTG[C/G]ATCATGTTTGTGGTG | 11137 |
rs755253889 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695709 | AAACCTTTTTTAAAA[A/G]TATTAAGAGTAATTT | 11137 |
rs755275391 | in-del | -/C | 1.6748e-05 | 0.00289374 | intron-variant | PWP1 | GRCh38.p7 | 12:107699337 | TTATTATGAGGGGGA[-/C]TTTAATACAAAAAAT | 11137 |
rs755351878 | snp | A/C | 0.000441194 | 0.014846 | intron-variant | PWP1 | GRCh38.p7 | 12:107710535 | TTTAGTTCTCTGCAC[A/C]CCTCCCCCTGCCCCT | 11137 |
rs755451331 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701821 | TAGCTGGGATTACTG[A/G]TGCATGCCACCATGC | 11137 |
rs755471521 | in-del | -/CTTTC | 4.95806e-05 | 0.00497874 | intron-variant | PWP1 | GRCh38.p7 | 12:107709036 | GCAAGAGTAATGCTT[-/CTTTC]ATTTTTCTTAACTTA | 11137 |
rs755504113 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702489 | TCACCATGTTGGCCA[A/G]GCTGGTCTTGAACTC | 11137 |
rs755609738 | snp | C/G | 1.65007e-05 | 0.00287229 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696482 | TTTTCAGTTTATAAT[C/G]AAGAAGAAGACTCTT | 11137 |
rs755613730 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711841 | GTAGAATAAGGCCAG[G/T]AGAGGGTCACTTATA | 11137 |
rs755725388 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698567 | CTTCCCTGTTCCTTG[C/T]AATGAAATTTTTTTC | 11137 |
rs755803884 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696583 | CCCAGATGATTCTAC[C/T]GGTAATTAGAAAACT | 11137 |
rs755813456 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710849 | GAGACAAGATCAGAT[A/G]TAATTGGTAATGTTT | 11137 |
rs755829843 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709922 | TTATATCCCAGAACA[C/T]AAACCGTGGTTACCT | 11137 |
rs755934299 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685838 | CGTGTGGCAGCAGTG[A/C]GGTCGTGGTCCCTCC | 11137 |
rs755980117 | snp | C/T | 1.68196e-05 | 0.00289992 | intron-variant | PWP1 | GRCh38.p7 | 12:107708907 | TAGCATGACCTTGCC[C/T]ATCTTTTACTCTTTC | 11137 |
rs756067972 | snp | C/T | 1.64961e-05 | 0.00287189 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704726 | AGTGACTTGGAATCA[C/T]TTTTCACCTTGTCAT | 11137 |
rs756141968 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699677 | GCCCTCTCTCCACCA[C/T]CACTGGAAAAAAACA | 11137 |
rs756338265 | snp | C/T | 1.65367e-05 | 0.00287543 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697555 | GCCAGTCTTCACACT[C/T]GGAAGTAAACTTTCA | 11137 |
rs756379742 | snp | A/C | 1.64833e-05 | 0.00287078 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709187 | GAAGATCTGGGACAT[A/C]TTAGGAGATAGGCCA | 11137 |
rs756478033 | snp | A/G | 1.65037e-05 | 0.00287256 | missense | PWP1 | GRCh38.p7 | 12:107703021 | CTAGCCTCGCTGTAC[A/G]CACAGACAAGGTATG | 11137 |
rs756507457 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701703 | GTTTTGTGTGAGACA[A/G]GGTCTTACTCTGTCA | 11137 |
rs756516267 | snp | A/G | 1.65293e-05 | 0.00287479 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712256 | GCTTACCTTAACTGG[A/G]AATTTTAAAAAGTTG | 11137 |
rs756582137 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706561 | GTCTTTAATCCATCT[G/T]GAATTAATTTTTGTA | 11137 |
rs756611179 | snp | G/T | 1.64855e-05 | 0.00287097 | intron-variant | PWP1 | GRCh38.p7 | 12:107703673 | CTCTGCATTTATGTT[G/T]CCTCCCTTTAGGTCC | 11137 |
rs756674523 | snp | A/C | 1.83927e-05 | 0.00303249 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688785 | ACTTAGATAAATATG[A/C]TGAGGAAGGTGACCC | 11137 |
rs756904472 | snp | A/T | 1.64827e-05 | 0.00287073 | missense | PWP1 | GRCh38.p7 | 12:107703686 | TTTCCTCCCTTTAGG[A/T]CCAAACACTGCAGTT | 11137 |
rs756954590 | snp | C/T | 1.66007e-05 | 0.00288098 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685885 | CTAGCGTGACACGCC[C/T]TTGACTTGAGGACCA | 11137 |
rs756982712 | snp | A/C | 1.66142e-05 | 0.00288216 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708928 | TTACTCTTTCTAGGC[A/C]AGTACAGATGACGGC | 11137 |
rs757134014 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698380 | AAAAAGAACTGCTAG[A/G]CCAGTCATAGTAGCT | 11137 |
rs757229494 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697215 | AGAGATTGAGCCTTT[A/C]CTACTCAAATTGTGG | 11137 |
rs757256697 | in-del | -/A | 1.64954e-05 | 0.00287183 | intron-variant | PWP1 | GRCh38.p7 | 12:107688568 | TGTGGTCTTGTTATT[-/A]AGAAGGTAGCATTTG | 11137 |
rs757365735 | snp | A/G | 3.3054e-05 | 0.00406521 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699426 | CCTTTCATGGAATAA[A/G]CTAATCAGGTAAAAA | 11137 |
rs757463509 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693288 | CAGTACATCACTTTG[A/G]TATCTGAATTTTCTA | 11137 |
rs757530537 | snp | A/G | 0.000353982 | 0.0132991 | intron-variant | PWP1 | GRCh38.p7 | 12:107697819 | TGTTCTTTCTTACAC[A/G]AAACTAGTTCAAAGC | 11137 |
rs757551840 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703952 | ATATAACTGTAGGAA[C/T]TAGCAACTTCTTTGG | 11137 |
rs757628472 | snp | A/C | 1.68764e-05 | 0.00290481 | intron-variant | PWP1 | GRCh38.p7 | 12:107692792 | CTATTTTATTATTGT[A/C]GTTTGTCAATTTTTC | 11137 |
rs757686722 | snp | A/G | 1.65083e-05 | 0.00287296 | intron-variant | PWP1 | GRCh38.p7 | 12:107703797 | TTTTATCCTCTAGAA[A/G]TCATTTTAAGAGTAT | 11137 |
rs757751655 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711763 | GTGAGTCCTAAGTCC[A/G]AAAAGTTCTGTGCCG | 11137 |
rs757860444 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694189 | CAATGTCTGGCGCAC[C/T]CTGCCTACAGATTCT | 11137 |
rs757877458 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694510 | GAAGCCTATAGATTA[C/G]GCCCATTTTATCTCA | 11137 |
rs757883172 | snp | A/C | | | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692898 | TTACTCTGAAAGATA[A/C]AGTAAGTATTTACAT | 11137 |
rs757884605 | in-del | -/TT | 1.65334e-05 | 0.00287514 | intron-variant | PWP1 | GRCh38.p7 | 12:107709248 | TAAGAATCTCCCTGG[-/TT]GTATCTGTTTTTTAT | 11137 |
rs757974055 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689776 | TGGGTGGGAAGAGAA[A/C]AAGGAAATAGAACAG | 11137 |
rs757998439 | snp | A/G | 1.64917e-05 | 0.00287151 | stop-gained | PWP1 | GRCh38.p7 | 12:107704687 | AAGCCATCGAATGTG[A/G]CGATTCAGTGGGCAG | 11137 |
rs758011074 | in-del | -/TTA | 0.000247891 | 0.0111303 | intron-variant | PWP1 | GRCh38.p7 | 12:107712080 | TAATTTCCTGATCTG[-/TTA]GTTTCTTACCTGTTT | 11137 |
rs758012327 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700705 | GCGTTATTACTGAAT[C/T]TTATGGTAATTCTAT | 11137 |
rs758022367 | snp | C/T | 1.67671e-05 | 0.00289539 | intron-variant | PWP1 | GRCh38.p7 | 12:107704603 | TAGGAGAATTGAACT[C/T]TTAAAACCCTAACTT | 11137 |
rs758104182 | snp | C/G | 1.74977e-05 | 0.00295779 | intron-variant | PWP1 | GRCh38.p7 | 12:107697424 | TTAGAAGTTCTGTAT[C/G]TCTTTTTTTGTGTAA | 11137 |
rs758242231 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697096 | TCTTGTTTGCACACC[A/T]TGTTCACATTCATGA | 11137 |
rs758297068 | snp | C/G | 1.65908e-05 | 0.00288012 | upstream-variant-2KB, utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107685935 | GACGTGCGTGGCCTG[C/G]GTCCGCTGCGGCGTG | 11137 |
rs758327987 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695862 | TATGAACATTATGAA[C/T]TTATGAACATTTGTT | 11137 |
rs758330774 | snp | A/T | 1.6519e-05 | 0.00287388 | intron-variant | PWP1 | GRCh38.p7 | 12:107709061 | TCTTAACTTATGATG[A/T]AGTAAATCTGTATTT | 11137 |
rs758348596 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708712 | CAGACCATTCACCAC[A/G]GCTTCATACTCATAT | 11137 |
rs758387572 | snp | A/T | 1.65053e-05 | 0.0028727 | missense | PWP1 | GRCh38.p7 | 12:107697537 | TATAGTGGACTCTTT[A/T]GAGCCAGTCTTCACA | 11137 |
rs758459336 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702766 | TAGATACTCTTGTTT[C/T]CTTTCATAATCTTCG | 11137 |
rs758489113 | snp | A/G | 9.9739e-05 | 0.00706113 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688741 | AGAGGATGACAGGAC[A/G]CTTGATGATGATGAG | 11137 |
rs758820503 | snp | C/T | 3.29679e-05 | 0.00405991 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693012 | TAGGAACAATATGAA[C/T]GTGAAGATTTCTTGA | 11137 |
rs758840576 | snp | A/G | 0.00018167 | 0.009529 | intron-variant | PWP1 | GRCh38.p7 | 12:107697839 | TAGTTCAAAGCTAGT[A/G]TATTAATATGAATAG | 11137 |
rs758856356 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691801 | TTCCTCCGTTTTCCT[C/T]ATTCGCTTGGCCATC | 11137 |
rs758909392 | in-del | -/AA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689312 | TATTTGATTCCTAGG[-/AA]TACATATAGGAAAAA | 11137 |
rs758934165 | in-del | -/GCTG | 1.68032e-05 | 0.0028985 | frameshift-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688756 | GCTTGATGATGATGA[-/GCTG]GCTGAGTACGACTTA | 11137 |
rs758970054 | snp | C/T | 4.95045e-05 | 0.00497492 | intron-variant | PWP1 | GRCh38.p7 | 12:107703636 | TGTTAGGTAATTTTA[C/T]GAAAAGCAAACCAAC | 11137 |
rs758989222 | in-del | -/A | 0.000180115 | 0.00948816 | intron-variant | PWP1 | GRCh38.p7 | 12:107697823 | TTTCTTACACAAAAC[-/A]TAGTTCAAAGCTAGT | 11137 |
rs759072503 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709529 | TTTTTTTTTTTTTTA[-/A]AACCCTGAAATCAAG | 11137 |
rs759122398 | snp | A/G | 1.65455e-05 | 0.00287619 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688727 | GAGGATGGTGACCCA[A/G]AGGATGACAGGACGC | 11137 |
rs759216869 | snp | A/G | 3.43018e-05 | 0.00414122 | intron-variant | PWP1 | GRCh38.p7 | 12:107708893 | TAGATTTTGTGACGT[A/G]GCATGACCTTGCCCA | 11137 |
rs759439163 | snp | A/T | 0.000253646 | 0.0112587 | intron-variant | PWP1 | GRCh38.p7 | 12:107710553 | TCCCCCTGCCCCTGT[A/T]AAAAAAAAAAAAAAA | 11137 |
rs759462964 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702035 | TTAGTACCCTTGTCA[A/G]AAACCAGTGACTATA | 11137 |
rs759470214 | in-del | -/TACAT | 3.35632e-05 | 0.0040964 | intron-variant | PWP1 | GRCh38.p7 | 12:107696442 | GATGACTCATTCTGA[-/TACAT]TAAAGTCTCTTTTCC | 11137 |
rs759472669 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691185 | AAGCCTTTAGTGCCA[C/G]AGCAATATTGAGCTT | 11137 |
rs759489108 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689615 | GCCAGGCGTGGTGGC[A/G]CACATCTGTAATCCC | 11137 |
rs759499506 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | PWP1 | GRCh38.p7 | 12:107702952 | ATGTTTTAGCAAGTG[C/T]ATCAGCTGACAACAC | 11137 |
rs759587321 | snp | A/T | 1.65201e-05 | 0.00287398 | missense | PWP1 | GRCh38.p7 | 12:107699399 | AGAAGGGCATACCGA[A/T]GCTGTCCTTGACCTT | 11137 |
rs759610817 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696947 | TTTAGAAAACATAAG[C/G]TAAAACCGAAATGAA | 11137 |
rs759646848 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | PWP1 | GRCh38.p7 | 12:107703667 | AGAGATCTCTGCATT[C/T]ATGTTTCCTCCCTTT | 11137 |
rs759689035 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710309 | TTGGTTTTGAATAAC[C/T]ATTTAAATCATAGAT | 11137 |
rs759717132 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | PWP1 | GRCh38.p7 | 12:107703779 | GAATGATTGCTACTC[C/T]GTTTTTATCCTCTAG | 11137 |
rs759723995 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698084 | ACTGCTAGGCCAGGC[A/C]ACGCACGTGGCTCAC | 11137 |
rs759779968 | snp | A/G | | | synonymous-codon | PWP1 | GRCh38.p7 | 12:107712193 | CCCTTTTGGCAGCAG[A/G]AGCTCAGATACACCC | 11137 |
rs759814442 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696563 | TGGCTGAATTTTGAT[A/C]CTAGCCCAGATGATT | 11137 |
rs759970576 | in-del | -/AA | 0.419266 | 0.183981 | intron-variant | PWP1 | GRCh38.p7 | 12:107710553 | TCCCCCTGCCCCTGT[-/AA]AAAAAAAAAAAAAAA | 11137 |
rs760032804 | snp | A/T | 1.65165e-05 | 0.00287367 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712250 | TTTCCTGCTTACCTT[A/T]ACTGGGAATTTTAAA | 11137 |
rs760051086 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696653 | CTAGCTCCATAAATT[A/T]TGTATTCTCTTGAAT | 11137 |
rs760139370 | snp | C/T | 6.64562e-05 | 0.005764 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107697489 | CATTGCTGTAGGAAA[C/T]ATGACCCCTGTTATT | 11137 |
rs760166971 | snp | A/G | 3.30568e-05 | 0.00406538 | intron-variant | PWP1 | GRCh38.p7 | 12:107709019 | GATGAAATCTCTGGT[A/G]AGCAAGAGTAATGCT | 11137 |
rs760275468 | snp | C/T | 1.65422e-05 | 0.0028759 | missense | PWP1 | GRCh38.p7 | 12:107697500 | GAAACATGACCCCTG[C/T]TATTGAAGTGTGGGA | 11137 |
rs760360760 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689430 | TACTGCCTGCATTTT[C/G]AGATGCTGTTCTTGG | 11137 |
rs760363308 | snp | A/G | 1.64985e-05 | 0.0028721 | splice-acceptor-variant | PWP1 | GRCh38.p7 | 12:107709110 | ACTTATCTTCCTTTA[A/G]GTCTTGATCTTAGCA | 11137 |
rs760407043 | snp | A/G | 4.95626e-05 | 0.00497784 | intron-variant | PWP1 | GRCh38.p7 | 12:107704628 | TAACTTTGCCTGAAT[A/G]TGTCTAGGTCAGTGG | 11137 |
rs760461654 | in-del | -/A | 3.31978e-05 | 0.00407404 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107697569 | CGGAAGTAAACTTTC[-/A]AAAAAAGAAGAAAAA | 11137 |
rs760491833 | snp | A/T | 2.26442e-05 | 0.00336475 | intron-variant | PWP1 | GRCh38.p7 | 12:107688818 | GTTAGTTTATCCACT[A/T]CTGATGGTTTGTAAT | 11137 |
rs760517195 | snp | A/C | 1.64852e-05 | 0.00287094 | missense | PWP1 | GRCh38.p7 | 12:107702961 | CAAGTGCATCAGCTG[A/C]CAACACTGTAATTCT | 11137 |
rs760667588 | snp | A/G | 1.64985e-05 | 0.0028721 | missense | PWP1 | GRCh38.p7 | 12:107704656 | TGGCTTTGTATGACT[A/G]CCGAAGTCCAGATGA | 11137 |
rs760712336 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712529 | AGGTAGTAATTTATA[A/G]AATTTTTAAAGCGTA | 11137 |
rs760806378 | snp | C/T | 6.59652e-05 | 0.00574267 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692881 | TGATCAAGATCCTTA[C/T]GTTACTCTGAAAGAT | 11137 |
rs760856390 | snp | C/T | 1.6501e-05 | 0.00287232 | intron-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692987 | TCAATGACATTTTTT[C/T]CCTCTCACTTAGGAA | 11137 |
rs760897133 | in-del | -/GG | 0.000150634 | 0.00867723 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107685997 | GTCGCTGGGAGACAA[-/GG]GGAGCAGCGTCTTTA | 11137 |
rs760952622 | snp | C/G | 1.66114e-05 | 0.00288192 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685870 | TATGCAGCCTGGTTT[C/G]TAGCGTGACACGCCC | 11137 |
rs761037727 | snp | G/T | 1.77037e-05 | 0.00297515 | intron-variant | PWP1 | GRCh38.p7 | 12:107697637 | ACTCTAATGACAGAG[G/T]TAAGTTTACTCGGGA | 11137 |
rs761187546 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | PWP1 | GRCh38.p7 | 12:107703790 | ACTCTGTTTTTATCC[C/T]CTAGAAGTCATTTTA | 11137 |
rs761190851 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683830 | TAGAGACGGGGTTTC[A/C]CTACGTTGGCCAGGC | 11137 |
rs761227223 | snp | A/G | 1.65124e-05 | 0.00287331 | missense | PWP1 | GRCh38.p7 | 12:107697514 | GTTATTGAAGTGTGG[A/G]ACCTTGATATAGTGG | 11137 |
rs761238189 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701204 | CAATCACTGCTCACT[G/T]TAGTCTTGACCTTCT | 11137 |
rs761273638 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696603 | ATTAGAAAACTTAAG[A/G]TTGTTCAATGATTTC | 11137 |
rs761304092 | snp | C/T | 1.75606e-05 | 0.00296311 | intron-variant | PWP1 | GRCh38.p7 | 12:107688426 | TTACACATATTGTAA[C/T]GAAATCTTTGCTCTC | 11137 |
rs761387314 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703449 | CTTCTAACATTTGAG[A/G]GACTAAGTATTCTGC | 11137 |
rs761405123 | snp | A/G | 1.66349e-05 | 0.00288395 | utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107688462 | GGTAGAGCTGAGTAA[A/G]GAAGAAGTAAAACGC | 11137 |
rs761459318 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691606 | AAGGGATTGCAGAGG[C/T]AGCTGGGAGTTTAGC | 11137 |
rs761560192 | snp | C/T | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712482 | AATTCCTTAAACATA[C/T]CATCTGTCACAGTTA | 11137 |
rs761561208 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685187 | AGGATCGCTGTTTTC[A/C]CAGGTGTAAAACGGA | 11137 |
rs761563914 | snp | A/G | 1.81714e-05 | 0.0030142 | intron-variant | PWP1 | GRCh38.p7 | 12:107697649 | GAGGTAAGTTTACTC[A/G]GGAGTAGGGGTGAAG | 11137 |
rs761701297 | snp | G/T | 3.2993e-05 | 0.00406145 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692844 | GTGAATCTCTCTTGG[G/T]TCTTACGGTCTACGG | 11137 |
rs761728274 | in-del | -/CTC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707095 | CAGTGGTTTGTAGTT[-/CTC]CTTGAAGAGGTCCTT | 11137 |
rs761946450 | in-del | -/C | 1.66363e-05 | 0.00288407 | intron-variant | PWP1 | GRCh38.p7 | 12:107704610 | ATTGAACTCTTAAAA[-/C]CCTAACTTTGCCTGA | 11137 |
rs761953676 | snp | A/T | 1.65463e-05 | 0.00287626 | intron-variant | PWP1 | GRCh38.p7 | 12:107712066 | TTTATATTCTGACTT[A/T]ATTTCCTGATCTGTT | 11137 |
rs761964210 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698832 | TCCCGGCCTCAAGCG[A/G]TGTTCCCACGTTAGC | 11137 |
rs761971201 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700544 | ATAATATTCCATTGT[A/G]TGTAATGTATGTTAC | 11137 |
rs762046350 | in-del | -/AG | 0.000105891 | 0.0072756 | intron-variant | PWP1 | GRCh38.p7 | 12:107697633 | TTAAACTCTAATGAC[-/AG]AGGTAAGTTTACTCG | 11137 |
rs762168944 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | PWP1 | GRCh38.p7 | 12:107688607 | TCTTTTTCTTTCTGT[C/G]CTCATAGAGAAGAAG | 11137 |
rs762343437 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695208 | GAGGCAGGGCTTGCA[A/G]TGGGCTGAGATCGTG | 11137 |
rs762364041 | snp | C/G/T | 3.29757e-05 | 0.00406041 | missense, stop-gained, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693003 | CCTCTCACTTAGGAA[C/G/T]AATATGAACGTGAAG | 11137 |
rs762429199 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708155 | TCAGGTACGCAACTT[C/G]CAGAGATTATTTGCT | 11137 |
rs762545979 | snp | A/G | 1.65209e-05 | 0.00287405 | missense | PWP1 | GRCh38.p7 | 12:107699394 | TCAGCAGAAGGGCAT[A/G]CCGATGCTGTCCTTG | 11137 |
rs762599278 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695071 | CCATCCTGGCTAACA[C/T]GGTAAAACCCAGTCT | 11137 |
rs762660682 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701507 | TATCTAGCAAACCAT[C/T]GCTTAAGTCAGGGTC | 11137 |
rs762712072 | snp | A/G | 1.64939e-05 | 0.0028717 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688620 | GTGCTCATAGAGAAG[A/G]AGGTGGTGGCAGTGA | 11137 |
rs762740936 | snp | A/T | 1.70804e-05 | 0.00292232 | intron-variant | PWP1 | GRCh38.p7 | 12:107697706 | GGTATTCTTGGTGAG[A/T]TGGGGTAGGTAGTTA | 11137 |
rs762827640 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691424 | TTTTGAGCATGGAAC[A/G]CATAATAATGGAACA | 11137 |
rs762850619 | in-del | -/CCCTC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711692 | TGATTCCTGCATCCT[-/CCCTC]CCCTCCCATGCAAAA | 11137 |
rs762859540 | snp | C/G | 3.29679e-05 | 0.00405991 | missense | PWP1 | GRCh38.p7 | 12:107710460 | TTATTTATGCCTTTG[C/G]AGGTCAAAAAGAAGG | 11137 |
rs762872251 | in-del | -/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712731 | GTTTGATAAGTAAAA[-/G]TTACATGCCCCTGTT | 11137 |
rs762966615 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692762 | GTCATAGGAAATATG[C/T]TTTTGTCAAGATGAC | 11137 |
rs763077716 | snp | G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685714 | TTTTGTCCCCTCCTA[G/T]TTCTCATTCGGCGCC | 11137 |
rs763093092 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699173 | CTGAGGCAGGAGAAT[C/T]GCTTGAATCCAGGAG | 11137 |
rs763105107 | snp | A/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684569 | ACAAATAATCTGCCT[A/G]CACAAACAATGAGCA | 11137 |
rs763210428 | snp | A/C | 1.72767e-05 | 0.00293905 | intron-variant | PWP1 | GRCh38.p7 | 12:107708881 | TTTACCCATTGTTAG[A/C]TTTTGTGACGTAGCA | 11137 |
rs763234173 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702887 | TTTCTCATATTTAAT[C/G]CTCTTGACTTTTAAA | 11137 |
rs763315145 | in-del | -/CTTAA | 0.000198275 | 0.00995481 | intron-variant | PWP1 | GRCh38.p7 | 12:107709047 | GCTTCTTTCATTTTT[-/CTTAA]CTTATGATGAAGTAA | 11137 |
rs763347327 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694938 | GAATATTGATCTCAC[A/G]TGGTTAAGAGTATAT | 11137 |
rs763383975 | in-del | -/CTT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703875 | AAATTATTTGCACTA[-/CTT]ATTTTTCCTTTTAAC | 11137 |
rs763464173 | in-del | -/A/AA/AAA/AAAA | 0.684211 | 0.152624 | intron-variant | PWP1 | GRCh38.p7 | 12:107710552 | TCCCCCTGCCCCTGT[-/A/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 11137 |
rs763471580 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708000 | TTCATGAAGTAATGA[G/T]TCTGAGATACTTAAT | 11137 |
rs763474512 | snp | G/T | 1.64958e-05 | 0.00287187 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709115 | TCTTCCTTTAGGTCT[G/T]GATCTTAGCAGTCAA | 11137 |
rs763556500 | snp | A/G | 8.26849e-05 | 0.00642928 | intron-variant | PWP1 | GRCh38.p7 | 12:107696611 | ACTTAAGGTTGTTCA[A/G]TGATTTCCAGTCTTA | 11137 |
rs763591441 | snp | C/T | 3.55638e-05 | 0.00421671 | intron-variant | PWP1 | GRCh38.p7 | 12:107693147 | GTGATGGTAAAATAA[C/T]AAGTGAAATAGTTAC | 11137 |
rs763610619 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691489 | GAACAGGTTGGCAGA[G/T]AGGGTGAATCTCTTA | 11137 |
rs763710961 | snp | A/G | 8.26358e-05 | 0.00642737 | intron-variant | PWP1 | GRCh38.p7 | 12:107709025 | ATCTCTGGTGAGCAA[A/G]AGTAATGCTTCTTTC | 11137 |
rs763769539 | snp | A/G | 4.98219e-05 | 0.00499084 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688738 | CCCAGAGGATGACAG[A/G]ACGCTTGATGATGAT | 11137 |
rs763816007 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698302 | GGGAGGCAGAGGTTG[C/T]AGTGAGCTCACACCA | 11137 |
rs763822435 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699498 | GATCTTACCTCATGC[C/G]TACACTCATCTCTTT | 11137 |
rs763823377 | snp | A/T | 1.64844e-05 | 0.00287087 | missense | PWP1 | GRCh38.p7 | 12:107710473 | TGGAGGTCAAAAAGA[A/T]GGGCTTCGGGTCTGG | 11137 |
rs763858022 | snp | A/G | 8.24219e-05 | 0.00641905 | missense | PWP1 | GRCh38.p7 | 12:107702963 | AGTGCATCAGCTGAC[A/G]ACACTGTAATTCTGT | 11137 |
rs763932262 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708656 | TGTGTTCACGTGGAT[A/G]TAACTATGGCCTCTT | 11137 |
rs764104270 | snp | C/G | 2.36309e-05 | 0.00343728 | intron-variant | PWP1 | GRCh38.p7 | 12:107688824 | TTATCCACTTCTGAT[C/G]GTTTGTAATTACAAG | 11137 |
rs764119020 | in-del | -/A | 0.000131883 | 0.00811935 | frameshift-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693010 | CTTAGGAACAATATG[-/A]ACGTGAAGATTTCTT | 11137 |
rs764132731 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695528 | GGGGTTCTGACTAGT[A/G]GGTTCTGTTTTATCA | 11137 |
rs764138806 | snp | A/G | 3.29821e-05 | 0.00406078 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692882 | GATCAAGATCCTTAC[A/G]TTACTCTGAAAGATA | 11137 |
rs764154497 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709578 | GAACCTCAGGGCACC[A/G]TAGCTATTAGGGTCA | 11137 |
rs764207565 | snp | C/G | 1.65012e-05 | 0.00287234 | intron-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692989 | AATGACATTTTTTTC[C/G]TCTCACTTAGGAACA | 11137 |
rs764212335 | in-del | -/G | 1.69792e-05 | 0.00291364 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686020 | CGTCTTTACGGCACT[-/G]GGGGGTCCGCCCAGC | 11137 |
rs764314671 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694963 | GTATATTTTAAAGTA[C/T]TATTACCAGTTGCTG | 11137 |
rs764373193 | snp | A/G | 1.66051e-05 | 0.00288137 | intron-variant | PWP1 | GRCh38.p7 | 12:107710366 | ATATTAGCGCTTTCT[A/G]AAGAGATTGAAATCA | 11137 |
rs764420458 | in-del | -/AAAG | 1.67231e-05 | 0.00289159 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107697582 | TTCAAAAAAGAAGAA[-/AAAG]AAAGGAAAGAAGGTA | 11137 |
rs764421491 | snp | C/T | 1.70006e-05 | 0.00291548 | intron-variant | PWP1 | GRCh38.p7 | 12:107688441 | TGAAATCTTTGCTCT[C/T]TTACAGGTAGAGCTG | 11137 |
rs764511041 | snp | G/T | 1.66114e-05 | 0.00288192 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685871 | ATGCAGCCTGGTTTC[G/T]AGCGTGACACGCCCT | 11137 |
rs764601665 | snp | A/T | 3.30743e-05 | 0.00406645 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712263 | TTAACTGGGAATTTT[A/T]AAAAGTTGGCCTAAA | 11137 |
rs764608610 | snp | A/G | 1.81158e-05 | 0.00300958 | intron-variant | PWP1 | GRCh38.p7 | 12:107697650 | AGGTAAGTTTACTCG[A/G]GAGTAGGGGTGAAGG | 11137 |
rs764626588 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692906 | AAAGATACAGTAAGT[A/G]TTTACATCTTTTTTC | 11137 |
rs764684698 | snp | A/G | 1.66007e-05 | 0.00288098 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685897 | GCCCTTGACTTGAGG[A/G]CCATGAACCGCAGCC | 11137 |
rs764705682 | snp | A/G | 1.65067e-05 | 0.00287282 | intron-variant | PWP1 | GRCh38.p7 | 12:107703793 | CTGTTTTTATCCTCT[A/G]GAAGTCATTTTAAGA | 11137 |
rs764758489 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701469 | CTACTTTATTTCTTT[C/T]GTTGTTCATGCTTTT | 11137 |
rs764848179 | snp | C/G | 1.651e-05 | 0.0028731 | missense | PWP1 | GRCh38.p7 | 12:107697517 | ATTGAAGTGTGGGAC[C/G]TTGATATAGTGGACT | 11137 |
rs764881362 | snp | A/G/T | 4.97998e-05 | 0.00498977 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688467 | AGCTGAGTAAAGAAG[A/G/T]AGTAAAACGCCTCAT | 11137 |
rs764921986 | in-del | -/AAG | 1.86565e-05 | 0.00305416 | intron-variant | PWP1 | GRCh38.p7 | 12:107710561 | CCCTGTAAAAAAAAA[-/AAG]AAAAAAAAAAAAGAC | 11137 |
rs764954997 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709406 | TTTATGACTTAGAAC[A/G]CTTTGTGGGGAATTC | 11137 |
rs765070373 | snp | A/G | 2.88238e-05 | 0.00379619 | intron-variant | PWP1 | GRCh38.p7 | 12:107688844 | GTAATTACAAGCTCA[A/G]TATGTTGGATCATGT | 11137 |
rs765084671 | in-del | -/GGGTTAGGCTAGTTAAC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711168 | CCGGATTAAAGGAAT[-/GGGTTAGGCTAGTTAAC]GGGTTAGGCTAGTTA | 11137 |
rs765212247 | snp | G/T | 1.64895e-05 | 0.00287132 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709148 | CAAGGGCTGTCTCGT[G/T]ACTGCTTCAGCTGAC | 11137 |
rs765258322 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710509 | AAGCACAGTCTCTTC[A/G]GGTAAGGATTTTTAG | 11137 |
rs765263145 | in-del | -/T | 3.54067e-05 | 0.00420739 | intron-variant | PWP1 | GRCh38.p7 | 12:107697637 | CTCTAATGACAGAGG[-/T]TAAGTTTACTCGGGA | 11137 |
rs765272135 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689647 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCAC | 11137 |
rs765427724 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698133 | TTAGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG | 11137 |
rs765444638 | in-del | -/AGAG | 1.64923e-05 | 0.00287156 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107704705 | ATTCAGTGGGCAGAT[-/AGAG]AGAGTGACTTGGAAT | 11137 |
rs765454711 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | PWP1 | GRCh38.p7 | 12:107712076 | GACTTAATTTCCTGA[C/T]CTGTTAGTTTCTTAC | 11137 |
rs765463701 | snp | A/G | 1.702e-05 | 0.00291714 | intron-variant | PWP1 | GRCh38.p7 | 12:107693121 | AAATCCCTTATTAAA[A/G]GATTTTCTAAGTGAT | 11137 |
rs765504503 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | PWP1 | GRCh38.p7 | 12:107699443 | TAATCAGGTAAAAAG[A/G]AATAACATTTGAATG | 11137 |
rs765512436 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710312 | GTTTTGAATAACCAT[G/T]TAAATCATAGATTCT | 11137 |
rs765562316 | in-del | -/TT/TTT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696029 | CATGATATTGGAATC[-/TT/TTT]TTTTTTTTTTTTTTT | 11137 |
rs765660170 | snp | G/T | 1.64917e-05 | 0.00287151 | missense | PWP1 | GRCh38.p7 | 12:107704680 | CAGATGAAAGCCATC[G/T]AATGTGGCGATTCAG | 11137 |
rs765722552 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702705 | TTTCCATATTAACAC[A/T]ATTAAGTCTTCTAAT | 11137 |
rs765748092 | snp | A/G | 1.70635e-05 | 0.00292087 | intron-variant | PWP1 | GRCh38.p7 | 12:107704587 | TTATAAATAAAACAT[A/G]TAGGAGAATTGAACT | 11137 |
rs765773194 | snp | A/T | 1.64947e-05 | 0.00287177 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688621 | TGCTCATAGAGAAGA[A/T]GGTGGTGGCAGTGAT | 11137 |
rs765839770 | snp | A/G | 1.66905e-05 | 0.00288876 | intron-variant | PWP1 | GRCh38.p7 | 12:107704783 | GTTTTGCTTTTCTAG[A/G]TTGCTAATGACTTTT | 11137 |
rs765853932 | in-del | -/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711391 | TTATGGCCAGATTTT[-/G]GGGGGGCTTGTTCCC | 11137 |
rs765929466 | snp | C/T | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712541 | ATAGAATTTTTAAAG[C/T]GTAAAATCCGGTAAT | 11137 |
rs765952702 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693970 | TTGGAACCAAAACAT[C/T]GTGATCACCTTTCTT | 11137 |
rs765961450 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705069 | TTTTAATGGCTAAAT[A/C]AGTCCAAGATGATAT | 11137 |
rs766072400 | in-del | -/AAG | | | cds-indel | PWP1 | GRCh38.p7 | 12:107696483 | TTTCAGTTTATAATC[-/AAG]AAGAAGACTCTTTTT | 11137 |
rs766162069 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689512 | GCACTTTGGGAGGCC[C/G]AGGCAGGTGGATCAC | 11137 |
rs766225745 | snp | A/T | 4.96973e-05 | 0.00498459 | intron-variant | PWP1 | GRCh38.p7 | 12:107709266 | ATCTGTTTTTTATTT[A/T]TTCTGTTTCTGACCT | 11137 |
rs766392451 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | PWP1 | GRCh38.p7 | 12:107702988 | TTCTGTGGGATATGT[C/T]CTTGGGGAAACCAGC | 11137 |
rs766423795 | snp | C/T | 1.9313e-05 | 0.00310743 | intron-variant | PWP1 | GRCh38.p7 | 12:107697727 | TAGGTAGTTATGAAA[C/T]TATTGTAATTTTTAG | 11137 |
rs766498959 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | PWP1 | GRCh38.p7 | 12:107712108 | TGTTTATTTGTATTT[C/T]AGTAAATGAAGCATT | 11137 |
rs766625396 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711178 | AGGAATGGGTTAGGC[C/T]AGTTAACTGCAGCAG | 11137 |
rs766672571 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702391 | GTTCAAGCTATTCTC[A/G]TGCCTCAGCCTCCTG | 11137 |
rs766725036 | snp | A/G | 1.68493e-05 | 0.00290248 | intron-variant | PWP1 | GRCh38.p7 | 12:107696427 | CGGGATGTGATTTTT[A/G]ATGACTCATTCTGAT | 11137 |
rs767040941 | in-del | -/T | 1.65382e-05 | 0.00287556 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107708967 | TAATTTGGATGCACG[-/T]TCAGATAAGCCAATT | 11137 |
rs767079203 | snp | G/T | 1.67002e-05 | 0.00288961 | intron-variant | PWP1 | GRCh38.p7 | 12:107696451 | TTCTGATACATTAAA[G/T]TCTCTTTTCCCAATC | 11137 |
rs767164669 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685803 | TCTGCCCTGGCAGCG[A/G]CCCTGTGCAGATCCC | 11137 |
rs767198599 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701599 | ATGATCCATTTTGAG[-/T]TTTTTTTTGTGTGTA | 11137 |
rs767204466 | snp | A/G | 1.65518e-05 | 0.00287674 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688730 | GATGGTGACCCAGAG[A/G]ATGACAGGACGCTTG | 11137 |
rs767220710 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691615 | CAGAGGTAGCTGGGA[A/G]TTTAGCATCATCCTA | 11137 |
rs767254929 | snp | C/T | 4.94841e-05 | 0.00497389 | missense | PWP1 | GRCh38.p7 | 12:107710499 | TCTGGGATATAAGCA[C/T]AGTCTCTTCAGGTAA | 11137 |
rs767263845 | in-del | -/CT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709727 | ACTGTATGCCAACCA[-/CT]GAGTTATATAAGTTA | 11137 |
rs767327036 | in-del | -/CTTGA | 1.65982e-05 | 0.00288077 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685885 | CTAGCGTGACACGCC[-/CTTGA]CTTGAGGACCATGAA | 11137 |
rs767345154 | snp | A/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685517 | GAAGTCTACGGAACT[A/G]CAAGCAAAATAAAGA | 11137 |
rs767380669 | snp | C/T | 1.65168e-05 | 0.00287369 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699405 | GCATACCGATGCTGT[C/T]CTTGACCTTTCATGG | 11137 |
rs767542936 | snp | A/G/T | 4.94607e-05 | 0.00497276 | intron-variant | PWP1 | GRCh38.p7 | 12:107703670 | GATCTCTGCATTTAT[A/G/T]TTTCCTCCCTTTAGG | 11137 |
rs767576824 | snp | A/G | 8.24586e-05 | 0.00642047 | utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107688648 | TGATGAAGAGGAGAC[A/G]GGCAGTCCTTCAGAA | 11137 |
rs767593590 | snp | A/C | 4.95021e-05 | 0.0049748 | intron-variant | PWP1 | GRCh38.p7 | 12:107703786 | TGCTACTCTGTTTTT[A/C]TCCTCTAGAAGTCAT | 11137 |
rs767619615 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711561 | TTCTACAAAATCCAA[C/T]TTTCCGGAAGGGGCC | 11137 |
rs767646290 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694201 | CACTCTGCCTACAGA[G/T]TCTCCGTTTTGTTTT | 11137 |
rs767732374 | snp | C/T | 3.31609e-05 | 0.00407177 | intron-variant | PWP1 | GRCh38.p7 | 12:107710373 | CGCTTTCTGAAGAGA[C/T]TGAAATCACCATCTT | 11137 |
rs767899053 | snp | A/C | 1.65192e-05 | 0.00287391 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712251 | TTCCTGCTTACCTTA[A/C]CTGGGAATTTTAAAA | 11137 |
rs767935901 | snp | C/G/T | 0.000282434 | 0.0118806 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685863 | CCCTCCCTATGCAGC[C/G/T]TGGTTTCTAGCGTGA | 11137 |
rs767984546 | snp | A/G | 3.29636e-05 | 0.00405964 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696573 | TTGATCCTAGCCCAG[A/G]TGATTCTACTGGTAA | 11137 |
rs768105905 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703206 | GGTAGGTATAATGCC[C/G]ATCTTAGAGATGAAA | 11137 |
rs768115605 | snp | C/T | 0.000148492 | 0.00861532 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692838 | CTCTTGGTGAATCTC[C/T]CTTGGGTCTTACGGT | 11137 |
rs768186695 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692942 | ATGCTCTTAAGTGTT[C/G]AAAAAACCTTACTGG | 11137 |
rs768204947 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695220 | GCAGTGGGCTGAGAT[C/T]GTGTCACTGCACTCC | 11137 |
rs768362918 | in-del | -/TG | 1.64944e-05 | 0.00287175 | intron-variant | PWP1 | GRCh38.p7 | 12:107703779 | GAATGATTGCTACTC[-/TG]TTTTTATCCTCTAGA | 11137 |
rs768487642 | snp | A/T | 1.64841e-05 | 0.00287085 | stop-gained | PWP1 | GRCh38.p7 | 12:107703741 | GATTTCTGGCTCATA[A/T]GATAAGTAAGAAAGC | 11137 |
rs768502578 | snp | C/T | 0.000115381 | 0.00759455 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107712208 | GAGCTCAGATACACC[C/T]ATGGAGTCTTAATGA | 11137 |
rs768553694 | in-del | -/TG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706169 | ATGAGCATTTTTTCA[-/TG]TGTCTGTTGGCTGCA | 11137 |
rs768571340 | in-del | -/CT | 1.66327e-05 | 0.00288376 | intron-variant | PWP1 | GRCh38.p7 | 12:107710360 | ATCTAGATATTAGCG[-/CT]TTCTGAAGAGATTGA | 11137 |
rs768581069 | snp | C/T | 4.96052e-05 | 0.00497998 | intron-variant | PWP1 | GRCh38.p7 | 12:107710527 | TAAGGATTTTTAGTT[C/T]TCTGCACACCTCCCC | 11137 |
rs768622154 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693550 | TACTCCTGCTATAAA[A/G]AACCTGGAAGTAAAA | 11137 |
rs768773490 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698685 | AAACGCCTAGGCTCA[A/G]GAGATCCTGGGATTC | 11137 |
rs768786437 | snp | A/C | 1.67385e-05 | 0.00289292 | intron-variant | PWP1 | GRCh38.p7 | 12:107693110 | TGGTAAGTGATAAAT[A/C]CCTTATTAAAAGATT | 11137 |
rs768859333 | snp | G/T | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696519 | TACACCATGATATAC[G/T]CTTGTCTGCATATCC | 11137 |
rs768975190 | snp | A/G | 3.35115e-05 | 0.00409324 | intron-variant | PWP1 | GRCh38.p7 | 12:107699334 | GTTTTATTATGAGGG[A/G]GACTTTAATACAAAA | 11137 |
rs769026120 | snp | C/T | 1.65496e-05 | 0.00287655 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708952 | TGACGGCTTTGTATA[C/T]AATTTGGATGCACGT | 11137 |
rs769081529 | snp | C/T | 1.65037e-05 | 0.00287256 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688687 | GCAGAGTGCACGCAC[C/T]CAGGCACGCCCAAGA | 11137 |
rs769161127 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688896 | CTCTTAGATTTTATT[G/T]TTCTTGACATCAGTA | 11137 |
rs769171647 | snp | A/G | 1.64972e-05 | 0.00287199 | intron-variant | PWP1 | GRCh38.p7 | 12:107688584 | AGAAGGTAGCATTTG[A/G]GTGATTCTCTTTTTC | 11137 |
rs769490977 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696325 | GGCACGAGCCACTGC[A/G]CCCAGCCTGGAATCT | 11137 |
rs769497002 | snp | C/T | 1.65364e-05 | 0.0028754 | missense | PWP1 | GRCh38.p7 | 12:107699380 | TATTACAGAGTTCCT[C/T]AGCAGAAGGGCATAC | 11137 |
rs769545856 | snp | A/C | 4.95372e-05 | 0.00497656 | splice-acceptor-variant | PWP1 | GRCh38.p7 | 12:107704634 | TGCCTGAATGTGTCT[A/C]GGTCAGTGGCTTTGT | 11137 |
rs769546991 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692850 | CTCTCTTGGGTCTTA[C/T]GGTCTACGGGAGTAA | 11137 |
rs769626726 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702130 | TTGTTGTGATTGCTG[C/T]AGATTTTCAGTAAGT | 11137 |
rs769634343 | snp | A/T | 6.59587e-05 | 0.00574239 | intron-variant | PWP1 | GRCh38.p7 | 12:107703765 | AGAAAGCACAGCAAG[A/T]ATGATTGCTACTCTG | 11137 |
rs769635684 | in-del | -/TATT | 1.65018e-05 | 0.00287239 | intron-variant | PWP1 | GRCh38.p7 | 12:107692905 | GAAAGATACAGTAAG[-/TATT]TACATCTTTTTTCTA | 11137 |
rs769650955 | snp | C/T | 1.64882e-05 | 0.00287121 | stop-gained, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693069 | TGTGGCCGAGCTGAA[C/T]AGGACCAGTGCAATT | 11137 |
rs769730767 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687767 | CGGGCACGGTGGCTC[-/A]ACGCCTGTAATCCCA | 11137 |
rs769730901 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708059 | ATGCTGTTCTAGCCA[A/G]GCAGCCTGAAGCCTG | 11137 |
rs769732611 | in-del | -/C | 1.66019e-05 | 0.00288109 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712273 | ATTTTAAAAAGTTGG[-/C]CTAAAAATGTTCCAT | 11137 |
rs769744306 | snp | A/T | 3.30814e-05 | 0.00406689 | intron-variant | PWP1 | GRCh38.p7 | 12:107692963 | ACCTTACTGGCTCTC[A/T]GCTTCTAGTCAATGA | 11137 |
rs769828108 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699114 | AAATATAAAAATTAG[C/T]TGGGCATGGTGGCAT | 11137 |
rs769842976 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691270 | CTCGGCAAGTTGATC[G/T]GCATGAGTGAAGCAC | 11137 |
rs769948563 | in-del | -/CA | 3.2981e-05 | 0.00406071 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107710497 | GGTCTGGGATATAAG[-/CA]CAGTCTCTTCAGGTA | 11137 |
rs769959413 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696541 | TGCATATCCTCTGAG[C/T]GTGGAATGGCTGAAT | 11137 |
rs770032446 | snp | A/C | 1.65072e-05 | 0.00287286 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688697 | CGCACCCAGGCACGC[A/C]CAAGAGAGCCCCTGG | 11137 |
rs770053591 | in-del | -/TT | 8.4268e-05 | 0.00649052 | intron-variant | PWP1 | GRCh38.p7 | 12:107704795 | TAGGTTGCTAATGAC[-/TT]TTTAAATTCCATAGT | 11137 |
rs770054438 | snp | A/G | 1.65321e-05 | 0.00287502 | missense | PWP1 | GRCh38.p7 | 12:107708974 | GATGCACGTTCAGAT[A/G]AGCCAATTTTTACAC | 11137 |
rs770095437 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695074 | CCTGGCTAACACGGT[-/A]AAAACCCAGTCTCTA | 11137 |
rs770121134 | snp | C/G | 6.60655e-05 | 0.00574703 | intron-variant | PWP1 | GRCh38.p7 | 12:107702912 | TTTAAAAGATTACCT[C/G]ATTGGATTCTTCCCT | 11137 |
rs770152817 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693526 | ATTGCCTGTTTTTCA[C/T]TCCTCTCCTACTCCT | 11137 |
rs770246188 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703143 | TTTTATCTGGCTTGC[A/G]GCATGCTTTCACATG | 11137 |
rs770260494 | snp | C/T | 3.29962e-05 | 0.00406165 | intron-variant | PWP1 | GRCh38.p7 | 12:107688610 | TTTTCTTTCTGTGCT[C/T]ATAGAGAAGAAGGTG | 11137 |
rs770287957 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700250 | AGTTCAGTGGCTTTC[A/T]GTACATTCACAGAGT | 11137 |
rs770288820 | in-del | -/AAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686990 | AAAAAAAAAAAAAAA[-/AAAA]AAAAAAAAAATAGAA | 11137 |
rs770341929 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707781 | GATAAGCTTTTTGAT[A/G]TGCTGCTGGATTCGG | 11137 |
rs770350200 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685624 | TCACATGCAGTCCTG[A/C]AAAGCCTTTTCTCTA | 11137 |
rs770389011 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696182 | GGACTACAGGCACGT[A/T]CCACCACACCCAGCT | 11137 |
rs770478940 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708744 | CAGTAGACATGTCAA[C/T]TGAATTAGCCCATGT | 11137 |
rs770541286 | snp | C/G | 1.64757e-05 | 0.00287012 | missense | PWP1 | GRCh38.p7 | 12:107712149 | GAGAGGCTTGTTCTT[C/G]GGAGTGCAAGAAATT | 11137 |
rs770546499 | in-del | -/T | 1.65545e-05 | 0.00287697 | intron-variant | PWP1 | GRCh38.p7 | 12:107702896 | TTTAATGCTCTTGAC[-/T]TTTAAAAGATTACCT | 11137 |
rs770568941 | in-del | -/AA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710024 | TGTAAAAAAGAAAAC[-/AA]AAAGTTTAAAAATGA | 11137 |
rs770632814 | snp | C/T | 2.45384e-05 | 0.00350265 | intron-variant | PWP1 | GRCh38.p7 | 12:107710547 | CACACCTCCCCCTGC[C/T]CCTGTAAAAAAAAAA | 11137 |
rs770640857 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688715 | AGAGAGCCCCTGGAG[A/G]ATGGTGACCCAGAGG | 11137 |
rs770681134 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691439 | ACATAATAATGGAAC[A/G]TACACTTTAGGAAGT | 11137 |
rs770690776 | snp | A/G | 1.6588e-05 | 0.00287988 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693094 | GCAATTTAGAGGTGC[A/G]TGGTAAGTGATAAAT | 11137 |
rs770780680 | snp | C/G/T | 4.9513e-05 | 0.00497538 | intron-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692983 | CTAGTCAATGACATT[C/G/T]TTTTCCTCTCACTTA | 11137 |
rs770812973 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701992 | CCCATTTGTTAAGAC[A/T]TTTTTCCCCATTGAA | 11137 |
rs771006966 | snp | C/T | 3.29669e-05 | 0.00405984 | missense | PWP1 | GRCh38.p7 | 12:107710480 | CAAAAAGAAGGGCTT[C/T]GGGTCTGGGATATAA | 11137 |
rs771108513 | snp | A/G | 1.69628e-05 | 0.00291224 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107697467 | TGTTTCCTCCCATAG[A/G]AAATTACATTGCTGT | 11137 |
rs771159175 | snp | C/G | 1.65288e-05 | 0.00287474 | missense | PWP1 | GRCh38.p7 | 12:107708989 | AAGCCAATTTTTACA[C/G]TTAATGCACACAATG | 11137 |
rs771275065 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691915 | ACAGCTGGTGAAAGA[C/T]GGTGCTGAGTTTTGA | 11137 |
rs771291383 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690964 | GAGACATGGTCTGTG[C/T]TGGGCACAGGAAGAT | 11137 |
rs771311826 | snp | C/T | 1.68414e-05 | 0.0029018 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686012 | GGGGAGCAGCGTCTT[C/T]ACGGCACTGGGGGTC | 11137 |
rs771329055 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698985 | ATCAAAACAATAGGT[C/T]GGGTGCAGTAGCTCA | 11137 |
rs771347617 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711046 | CAGAGCAGACAGCCC[C/T]GAACAGAGATTTACC | 11137 |
rs771466772 | snp | G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685534 | AAGCAAAATAAAGAT[G/T]GGTGAAACTTTGCTT | 11137 |
rs771530896 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705308 | ATCCAGAGCAAAGAT[G/T]AGTTAAATTTGTTGC | 11137 |
rs771533127 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693851 | TATACTGGATAGACA[C/G]GTTTTTCTCATGTTT | 11137 |
rs771593183 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | PWP1 | GRCh38.p7 | 12:107703703 | CAAACACTGCAGTTT[C/T]ATCCATTTGAAGCAC | 11137 |
rs771689809 | snp | A/G | 2.08227e-05 | 0.0032266 | intron-variant | PWP1 | GRCh38.p7 | 12:107688806 | AAGGTGACCCAGGTT[A/G]GTTTATCCACTTCTG | 11137 |
rs771756352 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687637 | CAGTTGCGGTGGCTC[A/G]TGCCTGTAATCCTAG | 11137 |
rs771779097 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686469 | CTGGGAGATGAATAG[A/G]GAATTTCTTGCAGTA | 11137 |
rs771848884 | snp | A/G | 0.000335711 | 0.0129516 | intron-variant | PWP1 | GRCh38.p7 | 12:107710561 | CCCCTGTAAAAAAAA[A/G]AAAAAAAAAAAAGAC | 11137 |
rs771937374 | in-del | -/TT | 3.29717e-05 | 0.00406015 | frameshift-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696496 | TCAAGAAGAAGACTC[-/TT]TTTATGTACACCATG | 11137 |
rs771985668 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691035 | CTCTGGGTAGAGATG[G/T]GATTGACCAAAGTCA | 11137 |
rs772066549 | in-del | -/T | 0.000131865 | 0.00811882 | intron-variant | PWP1 | GRCh38.p7 | 12:107703680 | TTTATGTTTCCTCCC[-/T]TTAGGTCCAAACACT | 11137 |
rs772102868 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712504 | TCACAGTTAATCTAG[A/G]TTTGTAAATAGGTAG | 11137 |
rs772173337 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689372 | GTGGTTTTAGACCAC[C/G]ACTGAGGGTCTTGGA | 11137 |
rs772293695 | snp | C/T | 1.65751e-05 | 0.00287876 | missense | PWP1 | GRCh38.p7 | 12:107697494 | CTGTAGGAAACATGA[C/T]CCCTGTTATTGAAGT | 11137 |
rs772331320 | in-del | -/TGTT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690772 | ACATTGAGGAAATAG[-/TGTT]AACTGTTAAAGCAAG | 11137 |
rs772396962 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant | PWP1 | GRCh38.p7 | 12:107709239 | ATGAAAATGGTAAGA[A/G]TCTCCCTGGGTATCT | 11137 |
rs772484426 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | PWP1 | GRCh38.p7 | 12:107709099 | AAAGTGTCTAAACTT[A/G]TCTTCCTTTAGGTCT | 11137 |
rs772524042 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697679 | GGGTAAGACCGTACA[C/T]TTTTTCAATCAGGTA | 11137 |
rs772590731 | snp | C/T | 0.00012143 | 0.00779103 | intron-variant | PWP1 | GRCh38.p7 | 12:107697615 | AAAGAAGTTAATAAA[C/T]ATTTAAACTCTAATG | 11137 |
rs772647673 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694774 | GATCAAAGAGGAGCT[A/G]AGAAAGAAGTTAAAG | 11137 |
rs772683715 | snp | G/T | 4.94319e-05 | 0.00497127 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696549 | CTCTGAGTGTGGAAT[G/T]GCTGAATTTTGATCC | 11137 |
rs772722107 | snp | A/C | 4.94939e-05 | 0.00497439 | intron-variant | PWP1 | GRCh38.p7 | 12:107688611 | TTTCTTTCTGTGCTC[A/C]TAGAGAAGAAGGTGG | 11137 |
rs772733976 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693881 | TTTTAAATAGAGTTA[C/T]TTCAGATATTTCCCC | 11137 |
rs772781473 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704534 | AAACAGGCTTTAAAT[C/G]AATCTTGATTTCACA | 11137 |
rs772875397 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687434 | AATACTGATGTTTAT[A/G]TCCCACTCCCAAGTA | 11137 |
rs772881940 | snp | A/C | 1.64838e-05 | 0.00287083 | missense | PWP1 | GRCh38.p7 | 12:107710470 | CTTTGGAGGTCAAAA[A/C]GAAGGGCTTCGGGTC | 11137 |
rs772905649 | snp | A/C | 1.65015e-05 | 0.00287237 | intron-variant | PWP1 | GRCh38.p7 | 12:107702921 | TTACCTGATTGGATT[A/C]TTCCCTTTCTCAGAA | 11137 |
rs773021019 | snp | A/G/T | 3.30073e-05 | 0.00406236 | missense | PWP1 | GRCh38.p7 | 12:107704643 | GTGTCTAGGTCAGTG[A/G/T]CTTTGTATGACTGCC | 11137 |
rs773027565 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704887 | TGAAAGCATAAGGTG[-/T]TTTTTTTTTAAATAA | 11137 |
rs773137970 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701304 | GGCCTCCCTTTGCCT[A/G]TTTTTTGTGTTTGAT | 11137 |
rs773152598 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709035 | AGCAAGAGTAATGCT[G/T]CTTTCATTTTTCTTA | 11137 |
rs773199766 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690749 | GGGGAGAGGGAGAGT[C/T]GAAAATGACATTGAG | 11137 |
rs773242389 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712522 | TGTAAATAGGTAGTA[A/G]TTTATAGAATTTTTA | 11137 |
rs773250313 | snp | A/T | 1.6549e-05 | 0.0028765 | intron-variant | PWP1 | GRCh38.p7 | 12:107709256 | CTCCCTGGGTATCTG[A/T]TTTTTATTTATTCTG | 11137 |
rs773346967 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686742 | GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG | 11137 |
rs773405520 | snp | C/G | 8.24423e-05 | 0.00641984 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712225 | TGGAGTCTTAATGAA[C/G]ATCATCTAATTTCCT | 11137 |
rs773453205 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696542 | GCATATCCTCTGAGT[A/G]TGGAATGGCTGAATT | 11137 |
rs773485716 | in-del | -/TGT | 0.000148971 | 0.00862921 | intron-variant | PWP1 | GRCh38.p7 | 12:107704761 | TGGTAAGAGTACGAA[-/TGT]TGTTGTTTTGCTTTT | 11137 |
rs773539343 | in-del | -/T | 0.000131887 | 0.00811949 | intron-variant | PWP1 | GRCh38.p7 | 12:107703668 | AGATCTCTGCATTTA[-/T]TGTTTCCTCCCTTTA | 11137 |
rs773545120 | in-del | -/ATATAAGCACAGTCTCTTCAGGTAAGGATT/T | 0.00040444 | 0.0142156 | intron-variant | PWP1 | GRCh38.p7 | 12:107710551 | CTCCCCCTGCCCCTG[lengthTooLong]TAAAAAAAAAAAAAA | 11137 |
rs773568190 | snp | C/T | 1.65304e-05 | 0.00287488 | missense | PWP1 | GRCh38.p7 | 12:107708977 | GCACGTTCAGATAAG[C/T]CAATTTTTACACTTA | 11137 |
rs773737124 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697783 | CTTATTTCTGATTAC[A/G]TAAAACCTCCATTAT | 11137 |
rs773738723 | snp | A/G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699189 | GCTTGAATCCAGGAG[A/G/T]TGGAGGTTGCAGTGA | 11137 |
rs773832364 | snp | C/T | 1.69766e-05 | 0.00291342 | intron-variant | PWP1 | GRCh38.p7 | 12:107704799 | TTGCTAATGACTTTT[C/T]AAATTCCATAGTAGA | 11137 |
rs773849884 | in-del | -/AAAAAAAAAAAAAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686971 | TGAGACTCCGTCTCA[-/AAAAAAAAAAAAAAAAAAAA]AAAAAAAAAATAGAA | 11137 |
rs773866418 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703300 | TCCTAAAAAAGGATG[A/G]GGTCTGTCAGTCACA | 11137 |
rs773867342 | in-del | -/AAT | 1.74199e-05 | 0.00295121 | intron-variant | PWP1 | GRCh38.p7 | 12:107693142 | TCTAAGTGATGGTAA[-/AAT]AATAAGTGAAATAGT | 11137 |
rs773894671 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696553 | GAGTGTGGAATGGCT[A/G]AATTTTGATCCTAGC | 11137 |
rs773903943 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692564 | TAAAAGGGTCTAATT[C/T]CCTGATACAGTTCTT | 11137 |
rs773941925 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688718 | GAGCCCCTGGAGGAT[A/G]GTGACCCAGAGGATG | 11137 |
rs774029350 | snp | A/G | 3.29707e-05 | 0.00406008 | missense | PWP1 | GRCh38.p7 | 12:107702951 | AATGTTTTAGCAAGT[A/G]CATCAGCTGACAACA | 11137 |
rs774054728 | snp | A/G | 1.66302e-05 | 0.00288355 | intron-variant | PWP1 | GRCh38.p7 | 12:107693101 | AGAGGTGCATGGTAA[A/G]TGATAAATCCCTTAT | 11137 |
rs774143503 | snp | C/T | 1.98592e-05 | 0.00315106 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688798 | TGATGAGGAAGGTGA[C/T]CCAGGTTAGTTTATC | 11137 |
rs774181037 | snp | C/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712385 | AAATATCCGGTCTTT[C/G]TGCTTGCTCTTCAGA | 11137 |
rs774302050 | snp | G/T | 1.65217e-05 | 0.00287412 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712249 | ATTTCCTGCTTACCT[G/T]AACTGGGAATTTTAA | 11137 |
rs774306718 | snp | A/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685059 | CGTCCAGCCACTCAC[A/G]AGTTCTAACAGATGA | 11137 |
rs774345430 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689059 | TTTAATAATCTGTAA[A/C]CCACTTGTGAGTTTT | 11137 |
rs774674351 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700537 | AGGCTAAATAATATT[A/C]CATTGTATGTAATGT | 11137 |
rs774707957 | snp | A/G | 1.6838e-05 | 0.0029015 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107697475 | CCCATAGGAAATTAC[A/G]TTGCTGTAGGAAACA | 11137 |
rs774709044 | snp | A/C | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696554 | AGTGTGGAATGGCTG[A/C]ATTTTGATCCTAGCC | 11137 |
rs774799413 | snp | A/T | 1.65285e-05 | 0.00287471 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708991 | GCCAATTTTTACACT[A/T]AATGCACACAATGAT | 11137 |
rs774822665 | in-del | -/AA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709528 | TTTTTTTTTTTTTTT[-/AA]AACCCTGAAATCAAG | 11137 |
rs774867825 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695030 | GGAGGCCAAGGCGGG[C/T]GGATCACGAGTTCAG | 11137 |
rs775048619 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702166 | TGCCAGGAAATATGA[A/G]CTTGCCAACTTTGTT | 11137 |
rs775169683 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692313 | TGCATTTCTTTTTTC[A/T]TATGCCAATAAGGCA | 11137 |
rs775177655 | snp | C/T | 1.65531e-05 | 0.00287686 | intron-variant | PWP1 | GRCh38.p7 | 12:107712060 | TGTCTTTTTATATTC[C/T]GACTTAATTTCCTGA | 11137 |
rs775184257 | snp | C/T | 2.23023e-05 | 0.00333926 | intron-variant | PWP1 | GRCh38.p7 | 12:107688816 | AGGTTAGTTTATCCA[C/T]TTCTGATGGTTTGTA | 11137 |
rs775256548 | snp | A/C | 1.64893e-05 | 0.0028713 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710425 | TCTCTTCTGTTCTTC[A/C]TGTTGCCCTGATTTG | 11137 |
rs775294296 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | PWP1 | GRCh38.p7 | 12:107712198 | TTGGCAGCAGGAGCT[C/T]AGATACACCCATGGA | 11137 |
rs775318559 | in-del | -/T | 3.50674e-05 | 0.00418718 | intron-variant | PWP1 | GRCh38.p7 | 12:107697427 | GAAGTTCTGTATGTC[-/T]TTTTTTGTGTAATCA | 11137 |
rs775377671 | in-del | -/TAAG | 1.64844e-05 | 0.00287087 | splice-donor-variant | PWP1 | GRCh38.p7 | 12:107703744 | TTCTGGCTCATATGA[-/TAAG]TAAGAAAGCACAGCA | 11137 |
rs775390104 | in-del | -/ATC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710180 | TCAGAAGTTGCAGAT[-/ATC]ATTGTGGAAGAACCA | 11137 |
rs775539355 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700279 | GTTGTGCAACCATCA[C/T]CACAATGCATCTCCA | 11137 |
rs775562875 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | PWP1 | GRCh38.p7 | 12:107704751 | TGTCATTTCTTGGTA[A/G]GAGTACGAATGTTGT | 11137 |
rs775606169 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691358 | AGTAAACTTAGAATA[C/T]CAGGCTTAGCAATCT | 11137 |
rs775715971 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707921 | TGGCCTCATAAAATG[A/T]GTTAGGGGGGAAAGA | 11137 |
rs775778218 | snp | C/T | 1.7402e-05 | 0.0029497 | intron-variant | PWP1 | GRCh38.p7 | 12:107697617 | AGAAGTTAATAAATA[C/T]TTAAACTCTAATGAC | 11137 |
rs775857099 | snp | A/G | 1.75959e-05 | 0.00296608 | intron-variant | PWP1 | GRCh38.p7 | 12:107688425 | CTTACACATATTGTA[A/G]TGAAATCTTTGCTCT | 11137 |
rs775864168 | snp | A/T | 1.6552e-05 | 0.00287676 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697498 | AGGAAACATGACCCC[A/T]GTTATTGAAGTGTGG | 11137 |
rs775866212 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | PWP1 | GRCh38.p7 | 12:107709242 | AAAATGGTAAGAATC[C/T]CCCTGGGTATCTGTT | 11137 |
rs775940406 | snp | A/G | | | splice-donor-variant | PWP1 | GRCh38.p7 | 12:107704748 | CCTTGTCATTTCTTG[A/G]TAAGAGTACGAATGT | 11137 |
rs775940957 | snp | G/T | 1.6536e-05 | 0.00287537 | intron-variant | PWP1 | GRCh38.p7 | 12:107709249 | TAAGAATCTCCCTGG[G/T]TATCTGTTTTTTATT | 11137 |
rs776111945 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686689 | AGAAAAAGTCCCGCC[A/G]GGCGCGGTGGCTCAC | 11137 |
rs776196947 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694937 | CGAATATTGATCTCA[C/T]GTGGTTAAGAGTATA | 11137 |
rs776219352 | snp | G/T | 2.47307e-05 | 0.00351636 | intron-variant | PWP1 | GRCh38.p7 | 12:107688829 | CACTTCTGATGGTTT[G/T]TAATTACAAGCTCAA | 11137 |
rs776255624 | snp | C/T | 5.43385e-05 | 0.00521213 | intron-variant | PWP1 | GRCh38.p7 | 12:107697648 | AGAGGTAAGTTTACT[C/T]GGGAGTAGGGGTGAA | 11137 |
rs776339188 | snp | C/T | 1.64885e-05 | 0.00287123 | intron-variant | PWP1 | GRCh38.p7 | 12:107703758 | ATAAGTAAGAAAGCA[C/T]AGCAAGAATGATTGC | 11137 |
rs776428500 | snp | C/T | 1.65971e-05 | 0.00288067 | intron-variant | PWP1 | GRCh38.p7 | 12:107703074 | TTCTTAAAAATCGGA[C/T]ACAAATATTGGCTAA | 11137 |
rs776448099 | in-del | -/AGG | 3.40933e-05 | 0.00412862 | intron-variant | PWP1 | GRCh38.p7 | 12:107704589 | ATAAATAAAACATAT[-/AGG]AGAATTGAACTCTTA | 11137 |
rs776502458 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691108 | AGCACAGTAGATAAC[A/G]TTGTGGAGGCAGAAC | 11137 |
rs776504314 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695037 | AAGGCGGGCGGATCA[C/T]GAGTTCAGGAGATCG | 11137 |
rs776569396 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697950 | TTTAAAAAAATTTCT[G/T]TTATCATGTTGAATT | 11137 |
rs776590833 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689538 | ATCACTTGAGGTCAG[C/G]AGTTCGAGACCAGCC | 11137 |
rs776594747 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702015 | CCATTGAACATTTAA[C/T]TACCTTAGTACCCTT | 11137 |
rs776614694 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692839 | TCTTGGTGAATCTCT[C/T]TTGGGTCTTACGGTC | 11137 |
rs776701941 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696528 | ATATACTCTTGTCTG[C/T]ATATCCTCTGAGTGT | 11137 |
rs776717722 | snp | C/G | 5.0255e-05 | 0.00501248 | intron-variant | PWP1 | GRCh38.p7 | 12:107693112 | GTAAGTGATAAATCC[C/G]TTATTAAAAGATTTT | 11137 |
rs776793810 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | PWP1 | GRCh38.p7 | 12:107709224 | GTTCATTCTAGGGAC[A/G]TGAAAATGGTAAGAA | 11137 |
rs776885207 | snp | A/G | 3.32563e-05 | 0.00407763 | intron-variant | PWP1 | GRCh38.p7 | 12:107704773 | GAATGTTGTTGTTTT[A/G]CTTTTCTAGGTTGCT | 11137 |
rs776921120 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | PWP1 | GRCh38.p7 | 12:107688592 | GCATTTGGGTGATTC[C/T]CTTTTTCTTTCTGTG | 11137 |
rs777008949 | snp | A/G | 1.68485e-05 | 0.00290241 | splice-acceptor-variant | PWP1 | GRCh38.p7 | 12:107688446 | TCTTTGCTCTCTTAC[A/G]GGTAGAGCTGAGTAA | 11137 |
rs777056526 | snp | G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684018 | GCCTTTCTTCTCTTT[G/T]GCCTTCTGCAGTGAT | 11137 |
rs777082054 | snp | A/G | 3.33673e-05 | 0.00408442 | intron-variant | PWP1 | GRCh38.p7 | 12:107699350 | GACTTTAATACAAAA[A/G]ATAATTAAAACAATT | 11137 |
rs777084869 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708737 | TCATATCCAGTAGAC[A/C]TGTCAACTGAATTAG | 11137 |
rs777145628 | in-del | -/TCA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694697 | TTAGAGTTTTTTTTG[-/TCA]TCATCGATTTTTTTA | 11137 |
rs777215632 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697663 | CGGGAGTAGGGGTGA[A/G]GGGTAAGACCGTACA | 11137 |
rs777247609 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699003 | GTGCAGTAGCTCACA[C/G]CTGTAATCCCAACAC | 11137 |
rs777258591 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692942 | TGCTCTTAAGTGTTC[-/A]AAAAAACCTTACTGG | 11137 |
rs777258926 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704669 | CTGCCGAAGTCCAGA[C/T]GAAAGCCATCGAATG | 11137 |
rs777313501 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696484 | TTCAGTTTATAATCA[A/G]GAAGAAGACTCTTTT | 11137 |
rs777550823 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688201 | CAAAACCAGTCTTTG[C/G]AGTTTTAAGACTAAG | 11137 |
rs777563790 | snp | G/T | 0.000132135 | 0.00812713 | missense | PWP1 | GRCh38.p7 | 12:107712143 | AGACGAGAGAGGCTT[G/T]TTCTTGGGAGTGCAA | 11137 |
rs777568883 | snp | C/G | 3.33072e-05 | 0.00408075 | intron-variant | PWP1 | GRCh38.p7 | 12:107708922 | CATCTTTTACTCTTT[C/G]TAGGCCAGTACAGAT | 11137 |
rs777660039 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697152 | CACCCCATGAAGGAG[A/G]ACGGGAGGAGGGTTA | 11137 |
rs777685782 | snp | A/G | 6.59816e-05 | 0.00574338 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688677 | AAGATGGCATGCAGA[A/G]TGCACGCACCCAGGC | 11137 |
rs777734695 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694576 | TTTAATGTGAAATTA[C/T]TCTTTCTAACTCTTG | 11137 |
rs777779716 | in-del | -/TGGAT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705111 | ATCCTCATGCTTAAA[-/TGGAT]TGGATCTCTAGTGAT | 11137 |
rs777938211 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | PWP1 | GRCh38.p7 | 12:107709067 | CTTATGATGAAGTAA[A/G]TCTGTATTTCAAAGC | 11137 |
rs777949386 | snp | C/T | 9.32844e-05 | 0.00682887 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688786 | CTTAGATAAATATGA[C/T]GAGGAAGGTGACCCA | 11137 |
rs778021642 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710999 | CAGAAATATAGAGAT[A/G]TGAAGTGGGAAATCA | 11137 |
rs778134603 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711684 | CCCACTGTATGATTC[C/T]TGCATCCTCCCTCCC | 11137 |
rs778135079 | snp | A/G | 1.65378e-05 | 0.00287552 | missense | PWP1 | GRCh38.p7 | 12:107697556 | CCAGTCTTCACACTC[A/G]GAAGTAAACTTTCAA | 11137 |
rs778150834 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant | PWP1 | GRCh38.p7 | 12:107703675 | CTGCATTTATGTTTC[C/T]TCCCTTTAGGTCCAA | 11137 |
rs778297462 | in-del | -/TTT | 3.29832e-05 | 0.00406085 | intron-variant | PWP1 | GRCh38.p7 | 12:107703653 | AAAGCAAACCAACAG[-/TTT]AGATCTCTGCATTTA | 11137 |
rs778307597 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107712151 | GAGGCTTGTTCTTGG[A/G]AGTGCAAGAAATTCA | 11137 |
rs778349209 | snp | A/G | 1.7156e-05 | 0.00292878 | intron-variant | PWP1 | GRCh38.p7 | 12:107692779 | TTTGTCAAGATGACT[A/G]TTTTATTATTGTAGT | 11137 |
rs778510949 | snp | G/T | 1.65452e-05 | 0.00287616 | intron-variant | PWP1 | GRCh38.p7 | 12:107703048 | TATGGTGATTTAGTT[G/T]ATCACAGCGGTTCTT | 11137 |
rs778526615 | snp | A/C | 1.65252e-05 | 0.00287443 | intron-variant | PWP1 | GRCh38.p7 | 12:107709050 | TCTTTCATTTTTCTT[A/C]ACTTATGATGAAGTA | 11137 |
rs778529996 | in-del | -/AGG | 1.64836e-05 | 0.0028708 | cds-indel | PWP1 | GRCh38.p7 | 12:107709190 | GATCTGGGACATCTT[-/AGG]AGATAGGCCAAGTCT | 11137 |
rs778656888 | in-del | -/TATG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705836 | CCACAATATGCACTA[-/TATG]TATGTGCACATATGC | 11137 |
rs778680784 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686249 | CTTAGCGGGCCGGAA[A/G]GGGGTGGGCTGCTGT | 11137 |
rs778686129 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699896 | CGAGGCTGGGTAATA[C/T]GTAAAGGAAAGAGGT | 11137 |
rs778713817 | snp | C/T | | | | | GRCh38.p7 | 12:107708649 | CCAGGCCTGTGTTCA[C/T]GTGGATGTAACTATG | 11137 |
rs778722765 | snp | G/T | 1.66043e-05 | 0.00288129 | | | GRCh38.p7 | 12:107696628 | GATTTCCAGTCTTAT[G/T]TATTTTCTCCTAGCT | 11137 |
rs778725132 | snp | A/G | 1.64789e-05 | 0.0028704 | | | GRCh38.p7 | 12:107696510 | CTTTTTATGTACACC[A/G]TGATATACTCTTGTC | 11137 |
rs778768655 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685454 | AATTCATTTTGGAGA[A/C]AGCTTTTTAAAAAAC | 11137 |
rs778802822 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694437 | TTGCTTCATCATGGC[C/T]TCCATTGATTAGCTT | 11137 |
rs778810475 | snp | A/C | 0.000180115 | 0.00948816 | intron-variant | PWP1 | GRCh38.p7 | 12:107697823 | CTTTCTTACACAAAA[A/C]TAGTTCAAAGCTAGT | 11137 |
rs778811268 | snp | C/T | 1.65773e-05 | 0.00287895 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708937 | CTAGGCCAGTACAGA[C/T]GACGGCTTTGTATAT | 11137 |
rs778880225 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701228 | ACCTTCTGGGGCTCA[C/G]GTGATCCTCCCACCT | 11137 |
rs778970178 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702423 | GTAACTGGGATTACA[A/G]GCATGCGCCACCATG | 11137 |
rs778982929 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701886 | TTTCACCATGTAGGC[C/T]AGGCTTGTCTCAAAC | 11137 |
rs779006289 | snp | A/G | 8.27657e-05 | 0.00643242 | intron-variant | PWP1 | GRCh38.p7 | 12:107710381 | GAAGAGATTGAAATC[A/G]CCATCTTCCTGTTCT | 11137 |
rs779364604 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691775 | TATCCATTTTTCCAT[C/G]TAGATGTTCATTCCT | 11137 |
rs779371026 | snp | A/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685267 | AACAGCGCCTTCAAC[A/G]TAAGTAAGCCCTTTG | 11137 |
rs779380731 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | PWP1 | GRCh38.p7 | 12:107709225 | TTCATTCTAGGGACA[C/T]GAAAATGGTAAGAAT | 11137 |
rs779383882 | snp | A/G | 1.65102e-05 | 0.00287312 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692899 | TACTCTGAAAGATAC[A/G]GTAAGTATTTACATC | 11137 |
rs779414109 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709990 | TTCTATAACAAATAT[A/G]TATTACCTATTAATA | 11137 |
rs779451882 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690172 | ACAAATGTTATCTGC[A/G]ACAAAGTAAAATCAC | 11137 |
rs779468364 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711920 | GGCAAAGAAAGTAAA[A/G]TACAAAAATAAATTG | 11137 |
rs779472914 | snp | A/C | 3.31559e-05 | 0.00407147 | intron-variant | PWP1 | GRCh38.p7 | 12:107692811 | TGTCAATTTTTCTTA[A/C]AGATGCTGAGACTCT | 11137 |
rs779473784 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | PWP1 | GRCh38.p7 | 12:107703731 | CACAGACTCTGATTT[C/T]TGGCTCATATGATAA | 11137 |
rs779487353 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709724 | CCTACTGTATGCCAA[C/G]CACTGAGTTATATAA | 11137 |
rs779494551 | in-del | -/CCATGTCTTGGATT | 1.6536e-05 | 0.00287537 | intron-variant | PWP1 | GRCh38.p7 | 12:107709249 | AAGAATCTCCCTGGG[-/CCATGTCTTGGATT]TATCTGTTTTTTATT | 11137 |
rs779526509 | in-del | -/TT | 1.64985e-05 | 0.0028721 | intron-variant | PWP1 | GRCh38.p7 | 12:107688594 | ATTTGGGTGATTCTC[-/TT]TTTCTTTCTGTGCTC | 11137 |
rs779544020 | in-del | -/TACC | 1.65113e-05 | 0.00287322 | intron-variant | PWP1 | GRCh38.p7 | 12:107712088 | GATCTGTTAGTTTCT[-/TACC]TACCTGTTTATTTGT | 11137 |
rs779555197 | snp | C/T | 3.32237e-05 | 0.00407563 | intron-variant | PWP1 | GRCh38.p7 | 12:107704611 | TTGAACTCTTAAAAC[C/T]CTAACTTTGCCTGAA | 11137 |
rs779617684 | in-del | -/AAAAAAAAAAAAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686970 | GTGAGACTCCGTCTC[-/AAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAATAG | 11137 |
rs779831543 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693530 | CCTGTTTTTCACTCC[A/T]CTCCTACTCCTGCTA | 11137 |
rs779860569 | snp | A/C | 1.65993e-05 | 0.00288086 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107685953 | CCGCTGCGGCGTGGC[A/C]AAAGAGACACCAGAC | 11137 |
rs779902328 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710935 | CCGAGACCAGCTCGG[C/T]TGGGGAGACCCTAAC | 11137 |
rs779943215 | snp | C/G | 1.65111e-05 | 0.0028732 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697546 | CTCTTTAGAGCCAGT[C/G]TTCACACTCGGAAGT | 11137 |
rs780231658 | snp | G/T | 1.64954e-05 | 0.00287183 | intron-variant | PWP1 | GRCh38.p7 | 12:107688568 | ATGTGGTCTTGTTAT[G/T]AGAAGGTAGCATTTG | 11137 |
rs780328607 | snp | C/T | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693049 | CCAGTGATAATCTTA[C/T]AGTTTGTGGCCGAGC | 11137 |
rs780335728 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689945 | GTTTCTTTTGGAATG[G/T]GCTACCCTAGGTGGC | 11137 |
rs780342052 | snp | C/G | 1.64955e-05 | 0.00287184 | missense | PWP1 | GRCh38.p7 | 12:107710411 | TCTCTCTAGGGAGTT[C/G]TCTTCTGTTCTTCAT | 11137 |
rs780355843 | in-del | -/AAG | 1.65436e-05 | 0.00287602 | intron-variant | PWP1 | GRCh38.p7 | 12:107699440 | AGCTAATCAGGTAAA[-/AAG]AAATAACATTTGAAT | 11137 |
rs780521739 | snp | A/G | 1.65463e-05 | 0.00287626 | intron-variant | PWP1 | GRCh38.p7 | 12:107710531 | GATTTTTAGTTCTCT[A/G]CACACCTCCCCCTGC | 11137 |
rs780571637 | in-del | -/AG | 1.75742e-05 | 0.00296425 | frameshift-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688774 | GGCTGAGTACGACTT[-/AG]ATAAATATGATGAGG | 11137 |
rs780606764 | snp | G/T | 1.65479e-05 | 0.0028764 | intron-variant | PWP1 | GRCh38.p7 | 12:107692959 | AAAAACCTTACTGGC[G/T]CTCTGCTTCTAGTCA | 11137 |
rs780700395 | in-del | -/ACA | 0.000212925 | 0.0103159 | intron-variant | PWP1 | GRCh38.p7 | 12:107697826 | CTTACACAAAACTAG[-/ACA]TTCAAAGCTAGTATA | 11137 |
rs780703367 | snp | C/G | 3.29701e-05 | 0.00406005 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693064 | TAGTTTGTGGCCGAG[C/G]TGAACAGGACCAGTG | 11137 |
rs780737720 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710028 | AAAAAAGAAAACAAA[A/G]TTTAAAAATGATTTA | 11137 |
rs780798259 | in-del | -/TGT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697801 | AAACCTCCATTATCA[-/TGT]TGTTCTTTCTTACAC | 11137 |
rs780867724 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709723 | ACCTACTGTATGCCA[A/G]CCACTGAGTTATATA | 11137 |
rs781092307 | snp | C/T | 9.91162e-05 | 0.00703905 | intron-variant | PWP1 | GRCh38.p7 | 12:107704629 | AACTTTGCCTGAATG[C/T]GTCTAGGTCAGTGGC | 11137 |
rs781179045 | snp | A/C | 1.67357e-05 | 0.00289268 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107685994 | CTGGTCGCTGGGAGA[A/C]AAGGGGAGCAGCGTC | 11137 |
rs781183182 | snp | C/T | 0.000154404 | 0.00878512 | intron-variant | PWP1 | GRCh38.p7 | 12:107697754 | TTAGTTTTGAAAAGG[C/T]CATCCAAAGAAAACT | 11137 |
rs781186422 | in-del | -/T | 1.64757e-05 | 0.00287012 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107712150 | GAGGCTTGTTCTTGG[-/T]GAGTGCAAGAAATTC | 11137 |
rs781246704 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700204 | GGACATAGCCAAATC[C/G]TATCACCATTTTTAC | 11137 |
rs781248031 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711190 | GGCTAGTTAACTGCA[A/G]CAGGAACATGCCCTT | 11137 |
rs781276923 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687217 | CCTGGGCACAGACTG[-/T]TTTATTTACTGTTTC | 11137 |
rs781298018 | snp | G/T | 3.55208e-05 | 0.00421416 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688775 | GCTGAGTACGACTTA[G/T]ATAAATATGATGAGG | 11137 |
rs781351544 | snp | G/T | 0.000416559 | 0.0144259 | intron-variant | PWP1 | GRCh38.p7 | 12:107699472 | TGATTGTAAAAGACT[G/T]TAGCCATTGTGATCT | 11137 |
rs781443937 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700191 | GAGATTTGGGTGGGG[A/G]CATAGCCAAATCCTA | 11137 |
rs781548341 | snp | A/G | 1.65214e-05 | 0.0028741 | intron-variant | PWP1 | GRCh38.p7 | 12:107709063 | TTAACTTATGATGAA[A/G]TAAATCTGTATTTCA | 11137 |
rs781555179 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | PWP1 | GRCh38.p7 | 12:107712122 | TTAGTAAATGAAGCA[C/T]TTGGAAGACGAGAGA | 11137 |
rs781565223 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700718 | ATCTTATGGTAATTC[C/T]ATTTTTAATTTTTTG | 11137 |
rs781569660 | in-del | -/G | 3.30396e-05 | 0.00406432 | frameshift-variant | PWP1 | GRCh38.p7 | 12:107699399 | GAAGGGCATACCGAT[-/G]GCTGTCCTTGACCTT | 11137 |
rs781623978 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691989 | TTCTATAGATACAGT[A/C]CAGCAGAGGATAGTT | 11137 |
rs781659412 | snp | C/T | 4.95168e-05 | 0.00497553 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688694 | GCACGCACCCAGGCA[C/T]GCCCAAGAGAGCCCC | 11137 |
rs796120110 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688337 | TTTGATTCTTATCTT[C/G]ATGACATTGCTTGGC | 11137 |
rs796191911 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692686 | TAGTTTCCTTTCCCA[A/G]CTCTAGATGATCCAG | 11137 |
rs796538244 | in-del | -/AAAAAAAAAAAAAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686981 | TCTCAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAA]TAGAAAAAGACCCTG | 11137 |
rs796758508 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698090 | AGGCCAGGCCACGCA[C/T]GTGGCTCACTCCTGT | 11137 |
rs796988252 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711774 | GTCCGAAAAGTTCTG[-/T]GCCGGTTATGATCAG | 11137 |