SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs149223130 | snp | C/G | 0.000461209 | 0.0151787 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667587 | ACCAGATCAGGAAGA[C/G]TGTATGTATTGGTAC | 317 |
rs149234579 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98699205 | TCTGCATTTTGGGCA[A/G]TGCTTCTAATTTTTT | 317 |
rs149283781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657451 | CAGACCATTGCTTAC[A/G]TCCTCTTTTCTGGGA | 317 |
rs149303143 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646070 | ATTTTGTTGTGGGTT[A/G]CAAAAGGTTTTGAGA | 317 |
rs149321598 | snp | A/G | 5.00755e-05 | 0.00500352 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662761 | GTTAATATGAAGAAG[A/G]CAGATTTGCCAGAAC | 317 |
rs149355843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676953 | CCTGGCTGAGAAGAG[C/T]AGCTTTAAAGTACAT | 317 |
rs149400694 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98704000 | ATGATTTTGTACTTA[C/T]CTGTTAAATTTTATG | 317 |
rs149446616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661186 | GATTACAGGCGTGAG[C/T]CACTGCGCTCGGCCC | 317 |
rs149563295 | snp | C/G/T | 0.0107246 | 0.0724382 | intron-variant | APAF1 | GRCh38.p7 | 12:98711813 | TTCTTCTCCATTGTC[C/G/T]TCACTGCCCCAGCTC | 317 |
rs149589840 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725516 | TACCCTGCTGGCAAC[A/G]GGAGATGACAATGGA | 317 |
rs149604516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666651 | TTCCGTCTCCTCAAA[C/T]CTGTGAAAATTTATC | 317 |
rs149631310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98728344 | CCCTCATCTTACTAG[C/T]CAGCTTTTTGAGGCT | 317 |
rs149672765 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650682 | GGTATAGACTATACT[C/G]TTGTCAGAAGTATGC | 317 |
rs149718728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705337 | AGAAAGTGGGAAGAG[A/G]GGGGAGGATTCTCAA | 317 |
rs149789132 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98695957 | TTTAATTTCTAGGAG[C/T]CTGCCTATTACTTGC | 317 |
rs149790641 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98725718 | CTCCACTGCAGAAAC[G/T]GATTCATTTTAGAGT | 317 |
rs149828175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684113 | TTTGAGAGGGGTAGT[A/G]AAAGACATTTCAGTT | 317 |
rs149861603 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98692374 | AGGCGTGAGCCACTG[C/T]ACCCAGCCTATGTTT | 317 |
rs149880887 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98715038 | TTCTCATCCAGGACT[G/T]ACTTACTTTCTTCTC | 317 |
rs149920083 | in-del | -/TC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674440 | GGTCTCTCTCTCTCT[-/TC]CTCTCTCTCTGAGAA | 317 |
rs149929649 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98669097 | TTTACATTTAATAGT[A/G]TATATTGGAATGATG | 317 |
rs149982140 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98701362 | CTTGTGTGTTTACCT[A/G]GGAGTGGAATTACTG | 317 |
rs150005477 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649523 | GTGGAGTACCACAGA[A/G]GCCAGTTGTTTTTGT | 317 |
rs150017979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98658617 | TATAAGAAAACCATA[A/G]TGGGTGAGTTATATG | 317 |
rs150045662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719385 | TGAGACAGTCTTGCT[C/T]TGTTGCCAGGCTGGA | 317 |
rs150056794 | snp | A/G | 0.000445916 | 0.0149251 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666356 | ATTGCAGCCAGCTTC[A/G]GGTACTTGCATCTTG | 317 |
rs150070471 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | APAF1 | GRCh38.p7 | 12:98655909 | CTGCCCCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 317 |
rs150158913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694230 | CAAATAATTTTTGGC[A/C]AAGTCCTCAAAAGCA | 317 |
rs150188379 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | APAF1 | GRCh38.p7 | 12:98676456 | TCAAGTGATCTGCCC[A/G]CCTCGTCCTCCCAAA | 317 |
rs150239970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98671278 | ATTGAAGTTTAAAAG[C/T]TAGGAAAATAAGATG | 317 |
rs150355642 | snp | A/C/T | 3.30908e-05 | 0.00406749 | synonymous-codon, stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686775 | AATCAAAAAGAATGT[A/C/T]GAAATACCATGTTTG | 317 |
rs150367992 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656688 | CTTAGAATATTCGCC[A/C/G]TCTTGCCTTATCTGA | 317 |
rs150369319 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729635 | AAAGCTTTTTCATTC[A/G]AAATTGATTCCTAAT | 317 |
rs150404772 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98652289 | ATACAAATACCAAAT[C/T]TGATTCCCCTCCAGT | 317 |
rs150457288 | snp | A/G | 0.000230624 | 0.0107359 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648430 | ACATCAAGACATCCT[A/G]CATCATGGATCACAT | 317 |
rs150517766 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98718569 | TTTCCTAAACTCCTT[A/G]GAGGAGTGGGGAAGT | 317 |
rs150574514 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98686543 | TTGAGTCCCTTAGTC[A/G]ATTTACATGCTGATC | 317 |
rs150592308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98673541 | AGCTTGAAATAATAA[A/G]TATGAGTGGCTCTCT | 317 |
rs150629452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662316 | GCAAAGAGGAAGAAT[C/T]ATTTTCCTAGATCTA | 317 |
rs150753355 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | APAF1 | GRCh38.p7 | 12:98664687 | TGCAGATACCCACCA[-/C]CACACCTGGGTAATT | 317 |
rs150784677 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98722801 | AGTGGGGCCAGGATC[A/T]GTAGACTTCCCCAGC | 317 |
rs150786881 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | APAF1 | GRCh38.p7 | 12:98668641 | TGGTATGCATTATAC[A/G]AGAAAGAGAAGAATC | 317 |
rs150803631 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98708523 | CATAGTTTGTCTCTC[A/G]CTTTAAGATGAAGAC | 317 |
rs150823984 | snp | C/T | 9.93032e-05 | 0.00704569 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648774 | TTCCTGTTGTCTCTT[C/T]TTCCAGTGGTAAAGA | 317 |
rs150839793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700951 | ATTTCTTCTTATGGC[C/T]GAATAATATTCCATT | 317 |
rs150892328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695519 | ACAGGTGTGCACCAC[C/T]ATGCCTGGCTAGAAG | 317 |
rs150954862 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | APAF1 | GRCh38.p7 | 12:98665107 | CTGTCATGGCTCACC[A/G]TAGCCTCAACCTCCT | 317 |
rs150962088 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98679261 | CCCCCTCTTTGCTGA[C/G]AGCTGTGCAGATGAC | 317 |
rs151008594 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734464 | ATTCAAAGATTTTTT[C/T]TGTTTCTGTAACTGG | 317 |
rs151013928 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732129 | TCTGGCCACTGCTGT[A/G]ATGGACTCTATAGCT | 317 |
rs151043372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656540 | TTGTTTGTTATATTT[G/T]AGACTTTCATGCAGT | 317 |
rs151055112 | in-del | -/TTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672154 | TGTTTCCATGAAGAT[-/TTTA]TTTATTTATTTATTT | 317 |
rs151098873 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98725640 | CAGGGAAGCATAGTC[C/G]TGAAGTTGTGGTTGG | 317 |
rs151139898 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659245 | GCAGAATCTTTGCAC[A/G]CGGTTGGATCAGGAT | 317 |
rs151167119 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98702565 | CGTGGTGGCTCACAC[C/T]GGTAATCCCAGCACT | 317 |
rs151175404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98714540 | GTAAGTGGCAGAGCT[A/G]GGATTCAAACCCAGA | 317 |
rs151219176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697064 | AACCAGATTGAACTT[A/G]TTCTTCTTTTTCATT | 317 |
rs151257034 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98693589 | CTCTCTCTTGTTAAT[A/T]TGCTCCTTAAATGAT | 317 |
rs151283247 | in-del | -/GAGAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689436 | CTTTTGTGTGAGGGT[-/GAGAGA]GAGAGAGAGAGAGAG | 317 |
rs151308317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98687562 | GAGATTTATTTCTTA[C/T]AGTTCTGGGGGAGAG | 317 |
rs180758034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670527 | ATGTGTTACAAATAA[A/G]TATTTTTTTAAAACT | 317 |
rs180763828 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98692334 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 317 |
rs180774473 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98712588 | GTGACACGATCACAG[C/G]CGACTGCAGCCTTGA | 317 |
rs180779783 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733751 | AGCAGTTCTTTTTGT[A/G]AAGTAAAACTTGTAT | 317 |
rs180802127 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98656915 | TATTGATGTAATCAC[C/T]GTCTCATTCATTGAC | 317 |
rs180805363 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98704157 | TTAATAGAAATGGGG[G/T]TCTCACTGTGTTGCC | 317 |
rs180824203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680706 | TAGGTATGAGCCACT[A/G]TGCGTGGCCTGAAAA | 317 |
rs180963620 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724539 | CATGCTGCTAACTTT[A/G]GTTTGATAAACCTTC | 317 |
rs181082442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700045 | TCAATGACTGAACAA[C/G]ATAGTGAAATTTTTA | 317 |
rs181083795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728455 | CCGGGTGTGGTGACT[C/T]ACACCTGTAATCCCA | 317 |
rs181084280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98676708 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 317 |
rs181107186 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98718939 | TCCCCATCTCAAATA[C/T]ATAATGGCCTTGTTC | 317 |
rs181171557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685997 | AAAATATTTAAGCAT[A/G]CATCTCAGAGATCTT | 317 |
rs181176992 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663994 | TCAAATAGACACACA[A/G]TTTTGTTTGTTTATT | 317 |
rs181179949 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649066 | TTAGAGACAATAAGA[C/T]AATTTATAGGCCCTT | 317 |
rs181188103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98707522 | GATATGATTTACTCC[C/T]TATTTCCAACACTCC | 317 |
rs181404427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654664 | CCCTCGCCTCGGCCT[C/T]CCAAAGTTCTGGGAT | 317 |
rs181407546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98679828 | CTGCAGCAGTCAGCA[C/T]GTCTGTGCGCAGTGG | 317 |
rs181407735 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98672723 | TTAATCTTCAAAACA[A/C]GTTTATAAGGTAAAT | 317 |
rs181413653 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98702780 | CAGTGAGCTGAGATC[G/T]CCCCAAGCTGAGATT | 317 |
rs181415158 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98724009 | TCAAATGCAACCTCT[A/G]CTGCATATTGTAGGC | 317 |
rs181461444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714091 | GCTTCCATCTCAGGC[A/T]CATCTCTCAAACTGT | 317 |
rs181532890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98676124 | TTTACTTGTACTCAA[A/G]GTGACAGGGATGTAA | 317 |
rs181535545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98648012 | TTTTTACATATGTAT[G/T]TGAATGTCTCCTTGA | 317 |
rs181546874 | snp | C/G | 0.00112048 | 0.0236429 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699486 | TTGGAGGACCCTCAA[C/G]AGGATATGGAAGTGA | 317 |
rs181594492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730104 | TAATTATCAATAAAA[A/T]TTTTTTTAAAAAAGA | 317 |
rs181602728 | snp | A/G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734514 | TAGTGTTAATAGTAG[A/G/T]TAACTTGTTTTTATT | 317 |
rs181776327 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98717990 | ATAAACCTGGCTGGC[A/T]GGTTCTCAGAGCTAA | 317 |
rs181826218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653423 | GCACTCTGGGAGGCC[A/G]AGGTGGACAGATCAT | 317 |
rs181831449 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98679483 | ACCACATTCTTCCTG[C/G]TTGTAGGACAAGAAC | 317 |
rs181990799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98693682 | TTGCTCCATTCTGGT[C/T]GGTAATGGTAATACT | 317 |
rs182000402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664510 | AGATTTAAAAAGTTG[A/G]GATTATGTATATGTG | 317 |
rs182019193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687081 | TAAAGTTCTATAATG[C/T]AGGCTGGGTGCGGTG | 317 |
rs182026131 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98729160 | TAGCAGAGGCTTCAC[C/T]TGGAGGGGAATGCTT | 317 |
rs182171961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675355 | GTAGATAGATCAAGC[A/C]GACATAAAGAACATT | 317 |
rs182205952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98713110 | AGGCATGAGCCACCA[C/T]ATCCAGCCTATTGTA | 317 |
rs182250616 | snp | C/T | 0.000569142 | 0.0168596 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644740 | GCCCAGGGCAGCTTC[C/T]TCACCAGGGGGAGCA | 317 |
rs182280587 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98671792 | TCAGGTGGTGAATAC[C/G]ATCACTCCAGGAGGA | 317 |
rs182293964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717617 | TGGACCTCAGGTGAT[A/C]CACCCACCTTGGCCT | 317 |
rs182340467 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98695148 | ACCTCTGCCTTTTGG[A/G]TTCAAGCAGTTCTCC | 317 |
rs182344899 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673295 | AGACCAGCCTGGTCA[A/T]CATGGTGAAACCCAT | 317 |
rs182363605 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735823 | AAATAAGTAAAATCT[A/G]TAGTGAATTTGGTGG | 317 |
rs182419493 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98647317 | GCTACTCAGAAGTAA[C/G]TCAAACATTTCGATG | 317 |
rs182489729 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98721259 | GCTATTCTTAATCTG[C/T]CCTCAGTGGTTGTCA | 317 |
rs182623143 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98705343 | TGGGAAGAGAGGGGA[G/T]GATTCTCAAGGGAGA | 317 |
rs182626466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725884 | GGAAAATAATTTTGT[A/C]AATTATGGTCTGGAT | 317 |
rs182638539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98660921 | GTATTTTTGGGAAAA[A/G]CCTACTAGGTGATTC | 317 |
rs182654671 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98705785 | TGAAATGAAGGTTAG[A/G]TGACAGTATTAGTGG | 317 |
rs182804545 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98688404 | GCAACCATCTAAGAT[A/G]CATTCTGCATCTCTT | 317 |
rs182811475 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644186 | GGACAGGAAGTAACG[C/G]TTTATAACAACGTGA | 317 |
rs182817905 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730843 | GTAGGTATCCAGAAG[C/T]TTAAAAAGTTCTTAA | 317 |
rs182914857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683525 | GTGTTCTCAGGCTCT[A/G]CCTCCCTTTCCATCT | 317 |
rs182931797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98677953 | GTAAATAGGAACTGG[A/G]CTAGACTATTTCCTA | 317 |
rs182936719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98650440 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 317 |
rs182948149 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701063 | CAATGTACAGATCAA[A/C]ACTCAAAATATTCCT | 317 |
rs182951511 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | APAF1 | GRCh38.p7 | 12:98720741 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 317 |
rs183070117 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98657948 | CTTTGTGCATATATA[C/T]AAGTATCTCTTTTGG | 317 |
rs183080362 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98704600 | ATCCATAGGCTTCTC[C/T]TAATTCTAGGTGCAG | 317 |
rs183082658 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98682042 | AACTAGAATGATGAT[C/T]AATTTTTTTGTTTTT | 317 |
rs183103159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708767 | TCTATTCACGGTTTT[G/T]CTTGTTTTTGGACTT | 317 |
rs183215749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98682450 | CTGCTACAGCTTGCA[A/G]GGTTAAGTGTCGATC | 317 |
rs183373356 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98665875 | GTTGTTACAGAGAAC[C/G]TTGGAAGGATAAGAC | 317 |
rs183444074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98659916 | TCATATGTACCATTG[C/T]AGGCTTTCAGGAAAT | 317 |
rs183486992 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688899 | GGCCCACCACAGTCT[A/G]TCTCCTGGGCTTAGA | 317 |
rs183487402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708226 | CTGGGATTACAGGTG[C/T]GAGCCCCTGCGCCTG | 317 |
rs183496932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712867 | TTGTTGCACAGGCTG[A/G]AGTGCAGTGGTACAA | 317 |
rs183506281 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98711118 | AGTACTTCTGGGGTG[A/C]ATTGGGATATGGAAT | 317 |
rs183509253 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731617 | GGGAAAGACAAAATG[C/T]TAGGTACTGCCATAG | 317 |
rs183510672 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734054 | AAATGTGAAATAGAA[C/T]AATTTTCATCTAATT | 317 |
rs183567561 | snp | A/G | 1.65261e-05 | 0.0028745 | intron-variant | APAF1 | GRCh38.p7 | 12:98667657 | AAGGTAAGATGACCC[A/G]TTTAAAAATTCTTTT | 317 |
rs183604251 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98687324 | CTGAGATCACGCCAC[A/T]CCACTCCAGCCTGGG | 317 |
rs183630730 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98717169 | CCCCGCACCTGGCCT[A/G]CTGTGCTCTATTTTT | 317 |
rs183650301 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645165 | CGCGCGGGCATGAGC[C/G]GTGGCAGGAGTGCGC | 317 |
rs183680203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695550 | AAATTTTAATCTCCT[A/G]TTTGTAGGATATGAC | 317 |
rs183700684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98698449 | ATTTATTTTTCTCTT[C/T]AGTATCAGGGAAGGC | 317 |
rs183703684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675270 | TCATTTGTTATTTGT[C/G]TAGTACTTTTGGGCC | 317 |
rs183894971 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98673598 | TAGAAGTCCAGGTTG[G/T]TATCTGTGATCTTTA | 317 |
rs183902207 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98716410 | CACTGTGTACTAAGG[A/G]TACTGTGAATGCATT | 317 |
rs183943858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670355 | TGGCCATCTGTGCTT[C/T]TTGTTTTGTGAATTG | 317 |
rs183945945 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98701593 | TGTGTTTTCCCAATT[A/G]CCAATGATGTTGAAC | 317 |
rs183966567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692086 | CTACTTTTTATGTTT[A/C]ATTATTATTTTTTTT | 317 |
rs184075036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98677171 | TTAATTAGATTTCTT[C/T]CAACTCAGTGACATT | 317 |
rs184085462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674177 | TTTATTTTTTTGTAG[A/C]GATAAGGTCTCACTA | 317 |
rs184090081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646072 | TTTGTTGTGGGTTAC[A/G]AAAGGTTTTGAGACT | 317 |
rs184092800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98719644 | AGCGTAAGCCACCAC[A/G]CCTGGCCACTTTTGA | 317 |
rs184104369 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98696528 | CACGAGTTTGGGTCA[G/T]GATAAATAAACCATC | 317 |
rs184106924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98717097 | CTGGTCTTGAACTCC[C/T]GACCTTGTGATCCGC | 317 |
rs184212839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650000 | ACTGGGTAGAAGAGG[A/G]TTTAAGAAATGTTGG | 317 |
rs184239133 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98700255 | AGGTTCAGAGCAGCC[A/G]AATGATTTGTCTAAA | 317 |
rs184542851 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98702570 | TGGCTCACACCGGTA[A/G]TCCCAGCACTTTGGG | 317 |
rs184542872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679540 | AAAAGAGCTGTAACA[C/T]AAACAGGGCTGAGAC | 317 |
rs184556575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98722919 | TGTTTTTTTTTTTCT[A/G]TCTTCTGGTATAATT | 317 |
rs184564621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646994 | ATGCTCTATTCACTC[G/T]TATGTTTGATAAGGA | 317 |
rs184575319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98652491 | TTAGCCTTTTGGGTT[G/T]CTTTTTTTATGGATT | 317 |
rs184626513 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653719 | ATATATATATATATA[G/T]ATATAGTTTTTAACT | 317 |
rs184729110 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98678531 | CCTGGGTGTAGCTGT[A/T]GCCGCCCAAACCACA | 317 |
rs184748337 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733685 | GTAATCCTCCTGCCT[C/T]AGCCTCCCAAAGTGT | 317 |
rs184754996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662278 | TTTTTCCTTATTTGA[A/G]TCAGCATATTGAGAA | 317 |
rs184823032 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98692440 | GATTCAGGGGTACAT[G/T]TGCAGGTTTGTTATG | 317 |
rs184855841 | snp | A/C | 1.64977e-05 | 0.00287203 | intron-variant | APAF1 | GRCh38.p7 | 12:98712293 | TCTTACAGCCTAATA[A/C]CTGATTTTGCCTCAT | 317 |
rs184877149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684265 | ATTTTTATTTATTTA[G/T]TTATTTTTTCAGAAG | 317 |
rs184884198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98706186 | TCCTAGAGATTTGTC[A/G]TCATCAAGGTGTTTT | 317 |
rs184890158 | snp | A/G | 4.94295e-05 | 0.00497115 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727194 | AATGTCTCAAACGGT[A/G]AGCTTCTTCATTTGT | 317 |
rs184902934 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684982 | AGCCAGTGAAAATAT[G/T]TAATTGTGAAGCTGC | 317 |
rs184936398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657311 | CCATCATTTTATTGT[C/T]CATCATTCAGTTGCT | 317 |
rs185017421 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98663293 | TTTTTGATATAAGTA[C/T]TTTTAATTTATTTCT | 317 |
rs185022806 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98707095 | GCAGCTTCTAAGATA[A/T]TTTTTTTTCATGTAC | 317 |
rs185027731 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98727865 | AGAATCGCTTGAACC[C/T]GGGAGGTGAAGGTTG | 317 |
rs185088412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98664043 | ATTTATTTTTTGAGA[C/T]GAGTCTCACTCTGTC | 317 |
rs185098033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98686462 | GATTCTAAACCACTC[C/T]GTTGAAATAAGTAGT | 317 |
rs185250557 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98669400 | CAGAAAAAAACGATG[A/G]AAAGGAAAACAGAGA | 317 |
rs185269114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98711651 | TGACAACTGATTTAA[A/G]CTTGAGAAATATTTT | 317 |
rs185285999 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733260 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 317 |
rs185360893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719030 | TGATGCCCTTATCCT[C/T]GTTCTACTCCATTGG | 317 |
rs185363907 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690260 | ACTCTTTCTGGGTAG[A/C]ATTCTACTTTGTAGA | 317 |
rs185511349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647930 | TACTCTAGCCTCCCA[A/G]TGTGCTGGGATTATA | 317 |
rs185534402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98698824 | TATTCAAGTGGTCCT[A/G]CTAGTGAGCAAAGTT | 317 |
rs185617788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694743 | CTGTTTGGATTTTAG[A/G]CATAGATATATCTTA | 317 |
rs185621968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98714740 | TTTAGCATCATCTGT[A/G]TTTTCCTTAGGCTTT | 317 |
rs185650890 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98675372 | ACATAAAGAACATTT[A/T]AAAATCTAATCCTCT | 317 |
rs185669463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717687 | GGCTTATATATATAA[C/T]TTTTTCCCCATAAAT | 317 |
rs185669852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678942 | CTCCCCTTGGCACCT[A/C]CAGCCTGGGTGCCAT | 317 |
rs185695524 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98672776 | TTATTTTTTTTGAGA[C/T]GGCGTTTCACTCTTG | 317 |
rs185696909 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98722046 | TTCTTTGGATACCTT[C/T]CCAACCTTTTTTCTC | 317 |
rs185699523 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644343 | GGAAATGAGATACAA[A/C/G]AAACGCCCGAAAGGG | 317 |
rs185699596 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724315 | CACCCTGAAGAGCAT[G/T]CTTTCCTCCTCCTCC | 317 |
rs185807574 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653022 | GATGTAGTCAAACTA[A/C]TCAGTTTTTTTTTTT | 317 |
rs185809992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98681018 | CAAACTAATAATTAC[A/G]TTACTGGTCTAAAAA | 317 |
rs185811596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98702226 | ACCTGCCACCGCGCC[C/T]GGCTAATTTTTTGTA | 317 |
rs185831216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98724639 | GTTTCCTGACCCTCA[A/G]GCAAGGTTAGCTGCT | 317 |
rs185840462 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98676141 | TGACAGGGATGTAAC[A/G]TATATGAAATTCTGT | 317 |
rs185846240 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98648200 | TTTGTCCATTTAAAA[A/G]TTTTTGCCAAGGAAA | 317 |
rs185895075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658084 | TGTTTTTTGCTTTTT[C/T]TGGTATGTTTAAGAT | 317 |
rs185912929 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | APAF1 | GRCh38.p7 | 12:98682060 | TTTTTTTGTTTTTTT[G/T]TTTTTTTTTTTGAGA | 317 |
rs185957642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699665 | ATTCATAAAAATAAA[A/G]TCTAGCTGTGTGATT | 317 |
rs185959166 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704213 | CAAGCAATACTCCCC[C/T]AGCCTTGGCCTCCCA | 317 |
rs185961833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718249 | CTTTCTTTTTTTTCT[G/T]TTTGAGACAGTCTTG | 317 |
rs185976672 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98707673 | AGTGCTTACTATATT[A/C]AAGACATTATGCAAA | 317 |
rs185990690 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98676780 | GCCTCCCAAGTAGCT[G/T]GGATTACAGGCACGT | 317 |
rs186017926 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98704746 | GTGGGCAGTGTTTTG[C/T]TGGGCAGAGACTTTG | 317 |
rs186023952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725700 | ATTGTATTCACAGCT[C/G]CACTCCACTGCAGAA | 317 |
rs186098781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649375 | CATTTTCTTAACTTC[G/T]CTTGGAAATTTTCAG | 317 |
rs186120537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98728679 | AGTCAGCTAAGGTCA[C/T]ACCACTGTACTCCAG | 317 |
rs186128629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700100 | AAAAGTAAATAAGAA[A/T]ATTCTTTGCTTTTCT | 317 |
rs186163005 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98708191 | CTCAGGTGATCTACC[C/T]GCCTTGGCCTCCCAA | 317 |
rs186167102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729667 | AGATCTTATGATACT[G/T]TTATTTCTTACTGAA | 317 |
rs186236712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664597 | GCTGGAGTGCAGTAA[A/G]ATCACAGCTCACTGC | 317 |
rs186256361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98687092 | AATGTAGGCTGGGTG[C/T]GGTGGCTCACGCCTG | 317 |
rs186272491 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735193 | CAAGAGGAGGATTTT[G/T]TTTTGTAGTTTGCAG | 317 |
rs186320516 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655663 | TTGTCACCTAGGCTG[C/G]AGTGCAGTGGCATGA | 317 |
rs186340198 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98702984 | GCTAATTTTATTTTA[A/G]CAAACCTCTGCTCTA | 317 |
rs186400502 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98671233 | TATTCTAATTAATTT[G/T]CTTCCTACCCTACTG | 317 |
rs186514675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680111 | TCTCTAGTTATGTGA[A/G]GGCATACACATTCTG | 317 |
rs186604035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684197 | TTATCTTTAGAAAGT[A/G]CTGAAACAGTTATTG | 317 |
rs186604592 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98688215 | CTCCAATAAGATTCC[C/G]AATTCCACTTTATTA | 317 |
rs186637838 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730366 | TGCTGACAAATTTAA[C/G]TGCTCAGCTTTGACA | 317 |
rs186672071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695518 | TACAGGTGTGCACCA[C/T]CATGCCTGGCTAGAA | 317 |
rs186684172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660952 | TGATGCATATTCGTT[A/G]TATTTTTATGGTGCA | 317 |
rs186685572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715904 | AATCCAATGGAAATC[A/G]TTTCATTCTTTCCTT | 317 |
rs186780826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672317 | TTATAGGCGCCCACC[A/C]CCATGCCTGTCTAGT | 317 |
rs186790076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98713173 | TATTAGTCATTGTTC[A/G]TTAAACTAACAATCA | 317 |
rs186842000 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98666111 | TAAGATACCGTTTTT[G/T]TGTGTGTGTGATAAT | 317 |
rs186855672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98708465 | TTTTGGATTATAATC[C/T]AATATTGAAACCTTT | 317 |
rs186942839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98674682 | AATCCCAGCTCTGCT[A/G]TTGATTAGTTGTGTA | 317 |
rs186943003 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646584 | CTTCTTTGAGTAGAC[G/T]GTGAATTATTTCAGG | 317 |
rs186944574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709435 | GAGCTCGGAGTGGTG[A/G]TAACAGATGCCCTAA | 317 |
rs186947775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98688765 | AAGCCTAGCCTACCA[C/T]TCTTTTCTTTTTTCT | 317 |
rs186951486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697006 | AGTGCTCTGAGAGCA[A/G]ATAAGGACTCTGTTG | 317 |
rs187000881 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694050 | CTCTATTCAATAAAT[A/G]GTGCTGGGATAACTG | 317 |
rs187010424 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734250 | TTCCTTCTTTCCTTT[C/T]TCTTCTTTTATCTCC | 317 |
rs187065429 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | APAF1 | GRCh38.p7 | 12:98717115 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 317 |
rs187212756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720899 | ATGAATCTGGGAGGC[A/G]AAGCTTGCAGTGAGC | 317 |
rs187275287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651072 | ATCTTGGAACAGGTT[G/T]TAACTACTTTGTTTT | 317 |
rs187281910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678198 | CTTTTGAGTTCCAGA[C/G]AGAATGCATATTAAA | 317 |
rs187283488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701110 | ACCTTATCCCCTAGC[C/T]GACCTATAATGGTTG | 317 |
rs187293155 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98720024 | CCATGACACTGGTGT[A/T]CTAGCTGTAAAACTC | 317 |
rs187443580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726652 | TTGCTCTGAGTTCGC[A/G]TCTTTGGATGAAAGT | 317 |
rs187456676 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733353 | GGCCGGGATGGTCTC[A/C/G]ATCTCTTGACCTCAT | 317 |
rs187496717 | snp | C/G | 0.00205227 | 0.0319675 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644747 | GCAGCTTCTTCACCA[C/G]GGGGAGCAGGACGTG | 317 |
rs187689494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98705803 | ACAGTATTAGTGGAA[A/G]ATAATCTGAATATGG | 317 |
rs187753923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673446 | GTCTCAAAAAACAAA[A/C]AAAAAAAAAACAAAA | 317 |
rs187756020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98678551 | CCCAAACCACAGCTG[C/T]AGGCTCGGGCCTCCG | 317 |
rs187767702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98721668 | CAGTTCGTCTTCTAA[A/G]GTTCTCTTGCTTGCA | 317 |
rs187823599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98689269 | TACCTTAATTGTCTG[C/T]TCTGGGCAAGGTGTT | 317 |
rs187835952 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98711461 | GCTCTTCGTAGTTCA[A/C/G]TTTTCATTTTGAATA | 317 |
rs187886733 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660243 | CCCAGCTACTCAGGA[C/G/T]GCTAAGGTGGGAGGA | 317 |
rs187907500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98705387 | AGGAGAGATTTTCAG[C/T]TGTGGAACCACTTTC | 317 |
rs187945549 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733032 | TTAGAGGTTTTTTGC[A/C]CTCTTTAAATTTGCT | 317 |
rs187977718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98664082 | TGGAGTGCAGTGGTG[C/T]GACCTCTGCTCACTG | 317 |
rs187987639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717398 | GTTTTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 317 |
rs187996744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707727 | ACATATAAATTTACT[A/G]ATTCTCACAATAGTC | 317 |
rs187998489 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98687065 | TGTACAACCTAATGC[A/T]TAAAGTTCTATAATG | 317 |
rs188021974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98652783 | AGGCACCCACCACCA[C/T]GCCTGGCTAATTTTG | 317 |
rs188039964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731377 | GTACATTTTTCGGGT[A/G]GTTGAACTAAGTGAT | 317 |
rs188178572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683377 | GGACTTTCTGGTCAC[A/G]ATGATAGAAACTACA | 317 |
rs188204092 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98726152 | TACAAACCATGCCAA[C/T]TTTATTTAGAAAACA | 317 |
rs188204280 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733469 | ACAGGGTCTTGCACT[A/G]TCACCCAGGCTGGAG | 317 |
rs188255012 | snp | A/G | 4.9489e-05 | 0.00497414 | intron-variant | APAF1 | GRCh38.p7 | 12:98712307 | AACTGATTTTGCCTC[A/G]TTTTTCATTAGCTCA | 317 |
rs188259081 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733738 | TGGCCTGGCCTTCAG[C/T]AGTTCTTTTTGTGAA | 317 |
rs188326364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670358 | CCATCTGTGCTTTTT[A/G]TTTTGTGAATTGTGG | 317 |
rs188348291 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | APAF1 | GRCh38.p7 | 12:98692143 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 317 |
rs188485208 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98712236 | CTGTGTTTTATTTTA[C/T]TTTTTTCAATTGAAG | 317 |
rs188526613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673732 | AGCATTTGAGTTTCT[C/G]TACTGTGCTAAGCAC | 317 |
rs188544441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98716926 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 317 |
rs188685164 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650182 | TCAAAGACAGTTCCC[A/G]ACTTCTAGTAGTTAA | 317 |
rs188689373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700793 | CTCTCTTGCTAGACC[C/T]TTGTAATCTCTAATG | 317 |
rs188691711 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98668191 | TGTTTTATTAGTATA[A/T]TTTTTTATTAGTAAA | 317 |
rs188703000 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645184 | GCAGGAGTGCGCGGC[C/G]GCAGCGGTGGCCGCC | 317 |
rs188829340 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695984 | TTGCCTTTCTGCTTT[C/G]TAGACTTGATGATTT | 317 |
rs188889043 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98654195 | ATGGTTAGAGATTTA[A/C]ATATCAGATGGTCAT | 317 |
rs188905358 | snp | C/T | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98702599 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 317 |
rs188909448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98679708 | GCTTCTGGGCACCAC[C/T]GTGTTCCCCGGTGCC | 317 |
rs188922163 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98723436 | TAATTTTTCTCATGC[C/T]TGTTTTCTGTTAATT | 317 |
rs188957525 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98677321 | GAATTTTGTATTTTG[A/G]GGAACATAACCATGT | 317 |
rs188974492 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98647186 | TTTCGGAGGCTGTGG[C/T]GGGTGGATCACCTGA | 317 |
rs189006089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698757 | GCTGAGACACTGCTC[A/T]TGGCCCAGAGGAGTG | 317 |
rs189133248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728985 | GCTCTGTGGCACAAT[A/G]TTTATGGCTTGGTTC | 317 |
rs189237320 | snp | C/T | 1.67002e-05 | 0.00288961 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662762 | TTAATATGAAGAAGG[C/T]AGATTTGCCAGAACA | 317 |
rs189247565 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98647994 | TAATTCTCCTTGTGG[A/T]TATTTTTACATATGT | 317 |
rs189255846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98684291 | AGAAGAAAAAATTAT[A/G]CAGAAGCTCAGTGTG | 317 |
rs189262154 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98706665 | TGGTGAGCTAAACCT[C/T]CTACAAACTAAGAAA | 317 |
rs189264233 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | APAF1 | GRCh38.p7 | 12:98727810 | GCCGGGCGTGGTGGC[A/G]TATGCCTGTAATCCC | 317 |
rs189274286 | snp | A/C | 0.000637958 | 0.0178486 | intron-variant | APAF1 | GRCh38.p7 | 12:98680252 | GCAGTTTATTATAAA[A/C]AATATTTTATTGTTA | 317 |
rs189281615 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98675272 | ATTTGTTATTTGTCT[A/T]GTACTTTTGGGCCAT | 317 |
rs189300695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98724421 | CCTTGTTGAAACACC[C/T]ATTACCTAACGGTTT | 317 |
rs189409398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98713079 | CCATCTTGGCCTCCC[A/G]GAGTGTTGGGATTAC | 317 |
rs189410462 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98679236 | CAGAGAGGAGCAACC[C/T]ACTCTAGTGCCCCCT | 317 |
rs189412496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98653320 | GGTTCCTATGGAAAT[A/G]TTTTCTTTGGGTGGT | 317 |
rs189639207 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98663684 | TTCTCTTTTGAGACA[A/T]GTCTCACTCTGTCGT | 317 |
rs189656929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98707506 | CTTGAATTTAAATAC[A/G]GATATGATTTACTCC | 317 |
rs189810553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98690536 | TCATCTTATCTCCTT[C/T]GCTAATTCCAAATTC | 317 |
rs189840257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710490 | GCAGAATAGAGAAGA[C/T]GAGAGTAATAGAGCA | 317 |
rs189842240 | snp | C/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731591 | AACATGCTTACTTGA[C/G]CCACTCACATGGGAA | 317 |
rs189898825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685190 | TTAGCATAAATCACC[A/G]GAGATGACTATAATC | 317 |
rs189924723 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728293 | AATAATAATAGCAGC[A/G]GTATATGGCTTTATA | 317 |
rs189963088 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672977 | TGGTCAGGCTGGTCT[C/T]GAACTCCAGACCTCA | 317 |
rs189967059 | snp | A/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644514 | CCAGGCAGCCTCGCG[A/T]CCACTTACCAGGCCA | 317 |
rs189972761 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98694848 | TAAATTGTGGTTTTC[C/T]TATGGGTTATCTGTT | 317 |
rs189986401 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98714963 | CCAGCCTTCTGATAT[C/T]CTGTCTCCCTCATCA | 317 |
rs189992637 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735473 | TTGTCATTTATCTGT[G/T]GATTAGACCACTAAA | 317 |
rs190055784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98669734 | AATTTCTGGGTCAAA[C/T]AGTATGTGCAGTTTA | 317 |
rs190106277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717737 | TGCTGTTCCCTCCAA[A/G]TTGCTTTTTTCTGTT | 317 |
rs190177024 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98676071 | TGTCTGACTGCCAAC[C/T]CTTGATTTCTAAAAT | 317 |
rs190326312 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98676452 | GACCTCAAGTGATCT[G/T]CCCGCCTCGTCCTCC | 317 |
rs190328340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98699675 | ATAAAGTCTAGCTGT[G/T]TGATTTTGGGCAGTC | 317 |
rs190332569 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98718637 | CTTATTTTCACGAGG[C/T]ATTAAAAATATGGCC | 317 |
rs190338731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98698827 | TCAAGTGGTCCTACT[A/G]GTGAGCAAAGTTTAC | 317 |
rs190448001 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98702328 | CCTTGGCCTCGCAAA[A/G]TGCTGGGATTACAGG | 317 |
rs190458717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98671459 | TTAAGCTTTTAAAGT[G/T]GCAAGATCACAGAAA | 317 |
rs190471272 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643366 | GGTCTCTTCTAAAAT[C/T]CTATCACTCTGGAAG | 317 |
rs190474973 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98682380 | TTTACTGAAAACTGA[A/G]CACTATAAGAGGCTA | 317 |
rs190479087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704929 | GGATTACAGGTGCCC[A/G]CCAGCATGCCCGGCT | 317 |
rs190482836 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98725737 | TCATTTTAGAGTTAG[A/T]GTGAAGCATTCCCTG | 317 |
rs190624207 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | APAF1 | GRCh38.p7 | 12:98708192 | TCAGGTGATCTACCC[A/G]CCTTGGCCTCCCAAA | 317 |
rs190624274 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677648 | TCAAGAAAATTGCAA[C/G]TTAGAAATAACAGAG | 317 |
rs190627194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649774 | GATAAATTGAATGGT[A/G]GAAACAAGTATAAGG | 317 |
rs190628301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98650341 | TACAAAAAAAATCAG[C/T]TGGGTGTGGTGGTGA | 317 |
rs190638351 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729860 | TTAGCTTTATGAAAG[G/T]ATGTACTAAGGGGTA | 317 |
rs190700105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722092 | GTCTCCTATGCTCTA[C/G]TCAGATGGACTCATG | 317 |
rs190702460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692678 | GCATTAATTTGCTTA[A/G]GATAATGGCCTCCAG | 317 |
rs190749655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700242 | AATGAGGCAACTGAG[A/G]TTCAGAGCAGCCAAA | 317 |
rs190974757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657787 | GTGTAACTTTGGGCA[A/G]ATTACTCAACTTTTC | 317 |
rs190985571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681192 | TCAGCCTCTTGAGTA[C/G]CTGAGATCACAGGTG | 317 |
rs190987686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704459 | AGCACTTCTTCAGTG[G/T]TCTCTGCTTATTTAG | 317 |
rs190993315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98676886 | CTGACCTCAGGTGAT[C/T]CACCCACCTTGGCCT | 317 |
rs191000434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98719329 | GGAGTTCATAATGCC[A/G]ATTTTGTTGCTTTAG | 317 |
rs191192176 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98708476 | AATCTAATATTGAAA[C/G]CTTTCTAGCATCATA | 317 |
rs191217501 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98655985 | AAACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 317 |
rs191282386 | snp | A/C | 1.64909e-05 | 0.00287144 | intron-variant | APAF1 | GRCh38.p7 | 12:98666140 | ATACCTGTCTACAGT[A/C]CTGGTCATTGTACTT | 317 |
rs191392578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667409 | GCGTGAGCCACCGAG[C/T]CCGGCCTCTCTGTAC | 317 |
rs191413685 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98688890 | CCTGATCCTGGCCCA[C/T]CACAGTCTATCTCCT | 317 |
rs191427642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688245 | ATTCCTGTCTCTATT[A/G]TCTCTCCTGTTTATT | 317 |
rs191436434 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730421 | TTGATTCTCTGGCCT[C/T]CACAGAATTCCATCA | 317 |
rs191531014 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98659634 | GCTCATGCCTGTAAT[A/C]CCAGCTGCTCAGGAG | 317 |
rs191538718 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646843 | ACTATAAAGGCTGTT[A/T]TTCTTTCCTCATGTC | 317 |
rs191539162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694365 | TCTTTCAATCTGGAA[A/G]CTTATCCTTCAGTTC | 317 |
rs191542921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98697154 | CCCTGGAGTGTTCCC[C/T]TGTCTTTTTGATGTT | 317 |
rs191547028 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98674814 | CATACATATAGTACT[C/T]AGAACAGCACCCAGT | 317 |
rs191552272 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734280 | CAAGGTTAATCAGGA[A/G]AAATAGCTTTTGACA | 317 |
rs191682576 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98652035 | ACCGAGGTTGGTCTC[A/G]AACTCCTGAGCTCAA | 317 |
rs191699859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701329 | CTGCAGCATTGGTGT[A/G]CAAGTATCTATTTGA | 317 |
rs191701684 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98678464 | GTAGCCGCCCAAGCC[A/G]CAGCTGTGGACCTGG | 317 |
rs191719132 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721089 | ATAGAGACATCCCCA[A/G]ACTCAACTTTTGCAT | 317 |
rs191796152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713227 | TTTCAGATTTCCTTT[A/G]TTACTGTTTCTCATG | 317 |
rs191835249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98720688 | GAAAAGTTTCCAGCC[A/G]GGTGCGGTGGCTCAC | 317 |
rs191974277 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98673478 | AAAAACCTTGGGTCT[A/G]CCTGGCTTTATTTTG | 317 |
rs191982390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664951 | TTCAACCACTTCTGT[A/G]TTATTGGACATTGTT | 317 |
rs191982666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98716189 | TACCTTCATGCCTCT[A/G]TATGGCATGCTTATA | 317 |
rs192032159 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701052 | CTTGTTGTAACCAAT[G/T]TACAGATCAAAACTC | 317 |
rs192062352 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645433 | GAGTAGCGCCGGGCT[C/T]CCTCCGGGGTGCAGC | 317 |
rs192071921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673780 | TCTTTCCCCTAAGGA[A/G]TTCAAAATCTCGTAG | 317 |
rs192074826 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98706968 | ACCTTTTCATTTTCT[A/G]TTATTATCTCTACCT | 317 |
rs192079817 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | APAF1 | GRCh38.p7 | 12:98727811 | CCGGGCGTGGTGGCA[C/T]ATGCCTGTAATCCCA | 317 |
rs192224878 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | APAF1 | GRCh38.p7 | 12:98702084 | CATTTTTTTTTTTTT[A/G]AGATGGAGTCTCGCT | 317 |
rs192293278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724955 | GACTAACATTTAAAG[A/T]TTACTTGTCACATGC | 317 |
rs192296186 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652853 | CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCC | 317 |
rs192298333 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98695545 | AGAAGAAATTTTAAT[C/T]TCCTATTTGTAGGAT | 317 |
rs192407003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98711498 | AGATCAAAATGTGCT[A/G]TGTAAAATAATGTTA | 317 |
rs192421145 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733244 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC | 317 |
rs192461619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98683498 | GCATAGCTGACTCCA[A/G]ATGCTTAAACTGTGT | 317 |
rs192530110 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98660988 | TGCTCACTGAAGCTC[C/T]GCTTCCTGGGTTCAA | 317 |
rs192544640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705955 | CCTATCCCTTCGCCT[C/T]GCTCTCCCTCCTTCC | 317 |
rs192545881 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684222 | TTATTGAAAATTGCC[A/G]TCTCCATCCCCCTGT | 317 |
rs192556619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98726809 | TATTCAGAATATAGG[A/G]AAGTTACTGATTTTT | 317 |
rs192587274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726369 | GAAAAGTTTGGGTAT[G/T]GGGATGACTACTTTG | 317 |
rs192650014 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722003 | CCCATACCTCAGAAT[A/T]TTAGCTTCATCAGGC | 317 |
rs192709057 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98678599 | GGACCCCTTCCCCCT[C/G]GTGCAGCTGTAGCTG | 317 |
rs192728631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670027 | TGAAATCACTGCAAC[C/T]GCCACTTCCTGGGCT | 317 |
rs192731229 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712265 | AGCCTCTGTTCTGAC[A/C/G]AACAAAAACTGCTCT | 317 |
rs192787984 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98660440 | AACTCTTCTACTTCC[A/G]TGTACTTCAGGAGTG | 317 |
rs192844595 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98705396 | TTTCAGTTGTGGAAC[C/G]ACTTTCATTTTTGGC | 317 |
rs192898520 | snp | A/G | 3.36564e-05 | 0.00410208 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662788 | GAACAAGCTCATAGT[A/G]TTATAAAAGAATGTA | 317 |
rs192902328 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98696365 | AACAACCCGCACTCT[A/T]GAGAACTAATCCATT | 317 |
rs192935446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98690596 | TGCCATTATTATTAG[A/G]TTGCCAAATGTTCAA | 317 |
rs192992501 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733547 | AAGCAATCCTCCTGC[C/T]TCAGCCTCCCAAGTA | 317 |
rs193028599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689846 | ATCTATAGGTAGAAA[C/G]TGCTTGGTTTGTCTT | 317 |
rs193046952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722677 | ATGCCTTCTCACTTC[C/T]GTCATTTTGAGGATT | 317 |
rs193060273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684833 | ACAGGAAAAAACCTC[C/T]GCCATGTGGGAGGGG | 317 |
rs193062215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98717010 | AGCTGGGATTACAGC[C/T]GTATGCCACCATGCC | 317 |
rs193218673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98668480 | AAGTCATTGCTCTCA[C/T]GAGTTTATGTTCTGG | 317 |
rs199525775 | snp | C/G/T | 3.29507e-05 | 0.00405887 | synonymous-codon, missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706581 | GATGGATCATCATTT[C/G/T]TGACATCTTCTGATG | 317 |
rs199621981 | in-del | -/T | 0.0970352 | 0.198 | intron-variant | APAF1 | GRCh38.p7 | 12:98671130 | TAAAAAGGAATCTCA[-/T]TTTTTTTTTACATTT | 317 |
rs199625521 | in-del | -/A | 0.24019 | 0.249807 | intron-variant | APAF1 | GRCh38.p7 | 12:98647254 | AACCCCGTCTGTACT[-/A]AAAAAAAAAAAAAAA | 317 |
rs199648389 | snp | A/G | 1.65381e-05 | 0.00287555 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665590 | AATTGGTGCACTTTT[A/G]CGTGATTTTCCCAAT | 317 |
rs199688058 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724895 | AGACAATATTGAAAG[A/G]AAAAAAAAATAGCAT | 317 |
rs199783677 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662550 | ACCAGAGACAAGAGT[A/G]TTACAGATTCAGTAA | 317 |
rs199795296 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673468 | AAAACAAAAAAAAAA[-/C]CTTGGGTCTGCCTGG | 317 |
rs199795679 | snp | A/T | 0.144296 | 0.226554 | intron-variant | APAF1 | GRCh38.p7 | 12:98715281 | ATATATATATATATA[A/T]GACATTCATTTGTTT | 317 |
rs199828818 | snp | A/T | 0.260227 | 0.249791 | intron-variant | APAF1 | GRCh38.p7 | 12:98689497 | GTGTGTGTGTGTGTG[A/T]GAGAGAGACACAGGG | 317 |
rs199829267 | in-del | -/T | 0.46754 | 0.123192 | intron-variant | APAF1 | GRCh38.p7 | 12:98723620 | GTCAACCTCCAAGTG[-/T]TTTTTTTTTTTTTTT | 317 |
rs199836156 | snp | A/G | 0.00523871 | 0.0509108 | intron-variant | APAF1 | GRCh38.p7 | 12:98699600 | AGCCAACTTCAGTCT[A/G]ATTTAAAGAAAGTTA | 317 |
rs199854014 | in-del | -/G | 0.000153794 | 0.00876773 | intron-variant | APAF1 | GRCh38.p7 | 12:98723623 | ACCTCCAAGTGTTTT[-/G]TTTTTTTTTTTTAAG | 317 |
rs199857372 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670189 | GCTCGAGTAATCCAC[C/T]CTCTTCAGCCTCTCA | 317 |
rs199944569 | snp | A/G | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648495 | GAAAAAGTAAGAAAT[A/G]AGGTAAAGCTCTCTG | 317 |
rs199965950 | snp | G/T | 1.66877e-05 | 0.00288852 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665519 | TGACAAAATAGGATG[G/T]TATTAGCATAGTGAC | 317 |
rs199967440 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664542 | TGCCCTTTTTTTTTT[-/T]AAAGAGCCAGGGTCT | 317 |
rs199975148 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671680 | CTAAGCTGCAGGCCA[A/G]GCAGGAGGTCGATAA | 317 |
rs200022669 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695056 | TTTCTTTTTCTTGCA[-/T]TTTTTTTCCCTCCCG | 317 |
rs200045670 | snp | A/T | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725576 | AGAGCACTGCTCTTC[A/T]TGTAGCTTGGGCTAG | 317 |
rs200051674 | in-del | -/ATAC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707711 | TATATATATATATAT[-/ATAC]ACATATAAATTTACT | 317 |
rs200058672 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660641 | ATTTCTGTCATCTTA[G/T]CAGCCTCTCTTTCAT | 317 |
rs200105604 | in-del | -/A | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98687584 | GGGGGAGAGGGTACC[-/A]GCAGAGAAGGGAGAG | 317 |
rs200116348 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688470 | ACCACTGTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 317 |
rs200169486 | snp | A/T | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665280 | TATATATATATATAT[A/T]TTTTTTTTTTTTTGT | 317 |
rs200196415 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654837 | TTTTTTTTTTTTTTA[A/T]TTTATTTTTTTATTG | 317 |
rs200206774 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695361 | AATGCCGCCCCCCCC[-/G]CTTTTTTTTTTTTGA | 317 |
rs200221100 | in-del | -/AGAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659778 | AAAAAAAAAAGAGAG[-/AGAA]AGAAAGAAAGAACCA | 317 |
rs200279687 | snp | C/G | 8.32993e-05 | 0.00645312 | intron-variant | APAF1 | GRCh38.p7 | 12:98665821 | GATCCTCATCATTGG[C/G]TATTTATTGCATGTA | 317 |
rs200295459 | snp | A/G | 0.00199806 | 0.0315442 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683143 | CTCTTTTCTCTTTAG[A/G]TTTGGAATTCTATGA | 317 |
rs200330421 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | APAF1 | GRCh38.p7 | 12:98667496 | TCTGGCTTCTGAAAC[A/G]TTTCATTGGGTTGCA | 317 |
rs200348381 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728996 | CAATGTTTATGGCTT[G/T]GTTCCTGCCTTTCAG | 317 |
rs200461221 | snp | C/T | 8.23839e-05 | 0.00641757 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703414 | TGGGAGAAATCCACA[C/T]GGGCCATCACAGCAC | 317 |
rs200511176 | in-del | -/A | 0.11963 | 0.213316 | intron-variant | APAF1 | GRCh38.p7 | 12:98654877 | GGGTGTTTCTCACAG[-/A]GGGGGATTTGGCAGG | 317 |
rs200521786 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694878 | TTTTATCATGAACAA[-/T]TTTTTTTTTTTTTTT | 317 |
rs200533513 | snp | A/C | 8.24097e-05 | 0.00641857 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649589 | AGCTCTCCAAATTGA[A/C]AGGTGAACCAGGATG | 317 |
rs200562772 | snp | A/G | 0.000148286 | 0.00860936 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686843 | AGATGATAAGCTTTT[A/G]GCTAGTTGTTCAGCT | 317 |
rs200621810 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648667 | GCTGATTAAAATGAT[A/G]CTTAAAAAAGATAAT | 317 |
rs200715583 | in-del | -/TATAT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665275 | ATATATATATATATA[-/TATAT]TTTTTTTTTTTTTTG | 317 |
rs200727659 | snp | C/T | 0.00199794 | 0.0315433 | intron-variant | APAF1 | GRCh38.p7 | 12:98708758 | GTTGAATTTTCTATT[C/T]ACGGTTTTTCTTGTT | 317 |
rs200729421 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669388 | TCATTGGAAAAACAG[A/G]AAAAAACGATGAAAA | 317 |
rs200771041 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662640 | ATATGTGACATACCA[A/G]ATTACTTACTTTGTC | 317 |
rs200776393 | snp | A/C/G | 4.94868e-05 | 0.00497407 | intron-variant | APAF1 | GRCh38.p7 | 12:98671515 | GATTGTGTTTCTAAG[A/C/G]GATTTCAGTTTATTT | 317 |
rs200811395 | snp | A/G | 0.000288426 | 0.0120054 | intron-variant | APAF1 | GRCh38.p7 | 12:98680411 | AGTGAAGGTAGGAAA[A/G]TCTTTTCCTCTTGAG | 317 |
rs200830441 | snp | A/G | 0.00034587 | 0.0131459 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659181 | TCCCAGGGGGAGTGC[A/G]TTGGGTTTCAGTTGG | 317 |
rs200907242 | in-del | -/A | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647027 | ACAAGAAGTCTCTTA[-/A]TATTAGGACTTCAAT | 317 |
rs200948182 | in-del | -/ACCTATT | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98724418 | GTCCCTTGTTGAAAC[-/ACCTATT]ACCTAACGGTTTATA | 317 |
rs200972415 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715760 | AATCCTCTGTTGGAA[-/G]GTTGTTTATTTTGAA | 317 |
rs200980865 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652688 | CTGGAGTGCCATGGC[G/T]CGATCTTGGCTCACC | 317 |
rs200996862 | snp | A/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647026 | AACAAGAAGTCTCTT[A/T]ATATTAGGACTTCAA | 317 |
rs201015522 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652635 | ATTTTATTTTATTTT[-/A]TTTTTTTTGAGACGG | 317 |
rs201029707 | snp | A/G/T | 0.000265604 | 0.0115212 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732492 | CTTAAGAAAATACAC[A/G/T]TGTCCCCTGACTTCA | 317 |
rs201047547 | snp | C/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643817 | TAATGATATGGTTTT[C/T]TTTTTTTTTTTTTTT | 317 |
rs201068722 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711926 | GTCTCAGTCTTGTTT[A/C]ACCAACAGCTTTGAA | 317 |
rs201068873 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702842 | GCAGAAGTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 317 |
rs201081099 | in-del | -/T | 0.0448719 | 0.142907 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735241 | TTTTCCCTTGCTGTA[-/T]TTTTTTTGTATTATA | 317 |
rs201107103 | snp | G/T | 0.000316353 | 0.0125728 | intron-variant | APAF1 | GRCh38.p7 | 12:98665818 | AATGATCCTCATCAT[G/T]GGGTATTTATTGCAT | 317 |
rs201122276 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715473 | AGTCCAGGTTTCAGC[A/G]CAAGAAAACTGTATG | 317 |
rs201251553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681242 | AATTTTTGTAGTTTT[A/G]GTAGAGACAGAGTTT | 317 |
rs201282564 | in-del | -/ATAT/ATTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672180 | TTTATTTATTTATTT[-/ATAT/ATTT]TTGAGACAGAGTCTC | 317 |
rs201296888 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667110 | TCTGTATATATATAT[A/G]TATTTTTTTTTTTTT | 317 |
rs201299555 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714724 | TTCTGGTGTCTCCTG[C/T]TTTAGCATCATCTGT | 317 |
rs201299622 | in-del | -/ATATATATATATATAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715236 | GCATACATGGTGTGC[-/ATATATATATATATAT]ATATATATATATATA | 317 |
rs201309144 | snp | A/C/G | 3.31252e-05 | 0.00406958 | intron-variant | APAF1 | GRCh38.p7 | 12:98662582 | GGGTAAGGATTATTC[A/C/G]TTTACTTTTTAGTAC | 317 |
rs201473140 | snp | A/G | 0.14665 | 0.227637 | intron-variant | APAF1 | GRCh38.p7 | 12:98715280 | TATATATATATATAT[A/G]TGACATTCATTTGTT | 317 |
rs201496530 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708252 | GCCTGGCCCAAACTT[-/C]TTACCTTGTGGATTG | 317 |
rs201499126 | snp | A/T | 1.67508e-05 | 0.00289398 | intron-variant | APAF1 | GRCh38.p7 | 12:98649441 | ATTACTTCAGTAATT[A/T]TTCCAAAGTTCTATT | 317 |
rs201519833 | snp | A/T | 1.648e-05 | 0.0028705 | intron-variant | APAF1 | GRCh38.p7 | 12:98667494 | TTTCTGGCTTCTGAA[A/T]CGTTTCATTGGGTTG | 317 |
rs201541593 | snp | A/G | 0.000149466 | 0.00864352 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715446 | TAGAACTTGTAAACA[A/G]TAGAATCTTCCAGTC | 317 |
rs201562861 | snp | A/C | 0.000533458 | 0.0163231 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662749 | TTATCCCTTTTTGTT[A/C]ATATGAAGAAGGCAG | 317 |
rs201583471 | snp | A/G | 0.000248783 | 0.0111503 | intron-variant | APAF1 | GRCh38.p7 | 12:98708561 | TTTAGAGATGGAATG[A/G]TAATTTCTTTATCTC | 317 |
rs201587280 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676665 | GTTTTTTTTTTTTTT[G/T]AAATGGAGTCTTGCT | 317 |
rs201605746 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | APAF1 | GRCh38.p7 | 12:98671756 | CCAAAGGGAGTGGTG[C/T]GCTAACTATATCATT | 317 |
rs201625604 | snp | A/G | 7.83546e-05 | 0.00625869 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644576 | CAGGCACGTTCGGGG[A/G]TCTGCCCAGCCCCCG | 317 |
rs201629052 | snp | A/C/G | 1.65231e-05 | 0.00287424 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665730 | AAATGCTCAGAGAAG[A/C/G]CATCAAAGATTATTA | 317 |
rs201678092 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725508 | GTGGACAGTACCCTG[C/T]TGGCAACGGGAGATG | 317 |
rs201698124 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691722 | CACCTAGTTTTTTTG[-/T]TTTTTTTGTGTTTTT | 317 |
rs201743914 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693957 | TGATTTGCTTGAGTT[-/C]CTTATGAATTCTGGA | 317 |
rs201755650 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723495 | GAGCATTTATACTGT[A/G]AGTCACATTTAAAGT | 317 |
rs201838716 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661905 | ACAACTGGGAACTGG[C/T]ATAGAGGTTCTTGGT | 317 |
rs201869264 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662344 | CTAGCCATCTATTTG[-/T]TTTAAAAAAAATTTA | 317 |
rs201872620 | snp | A/G | 3.29707e-05 | 0.00406008 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666296 | ATGGAAAGTCGTTTC[A/G]TTATTATTTACATGA | 317 |
rs201897485 | in-del | -/AT/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667099 | TCTGTATATATATAT[-/AT/TA]GTATTTTTTTTTTTT | 317 |
rs201911170 | snp | A/G | 1.64955e-05 | 0.00287184 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712329 | ATTAGCTCATTAATG[A/G]AAGAACAGGTCAGAT | 317 |
rs201917086 | snp | A/T | 0.00199792 | 0.0315431 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732467 | GACCTTCTACACAAA[A/T]GGAACCAATCTTAAG | 317 |
rs201932795 | snp | G/T | 0.000132072 | 0.00812518 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665692 | TTATGAGGCTCTAGA[G/T]GAAGCCATGTCTATA | 317 |
rs201949595 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667112 | TGTATATATATATGT[-/A]TTTTTTTTTTTTTGA | 317 |
rs201963658 | snp | C/G/T | 0.00199792 | 0.0315431 | intron-variant | APAF1 | GRCh38.p7 | 12:98666365 | AGCTTCAGGTACTTG[C/G/T]ATCTTGGTTTACTTT | 317 |
rs202065446 | snp | A/T | 0.000346446 | 0.0131569 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648694 | TAATGATTCCTACGT[A/T]TCATTCTACAATGCT | 317 |
rs202106733 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659771 | AAAAAAAAAAAAAAA[-/G]AGAGAGAGAAAGAAA | 317 |
rs202216630 | snp | A/G | 9.8881e-05 | 0.0070307 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699518 | AGTGAAGTGTTGTTC[A/G]TGGTCTGCTGATGGT | 317 |
rs202243082 | snp | A/C | 0.00199792 | 0.0315431 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671601 | CTTCTTGGACGACAG[A/C]CATTTCCTAATATTG | 317 |
rs202244203 | snp | C/T | 0.000249449 | 0.0111652 | intron-variant | APAF1 | GRCh38.p7 | 12:98648583 | CTACTTTATGTTGCA[C/T]ACATATTCATTGTTG | 317 |
rs367569272 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722501 | TTAGTAATTAAGAAA[C/T]GTCCTTTACATAGAC | 317 |
rs367578785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695928 | GCTTGGATTTCTCCA[C/T]TGCAGGCTCAGAATT | 317 |
rs367664693 | snp | A/G | 0.00209438 | 0.0322925 | intron-variant | APAF1 | GRCh38.p7 | 12:98649458 | TCCAAAGTTCTATTC[A/G]TTCATGCTTGTTTTG | 317 |
rs367677069 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670489 | TTTCTATAAAAATAA[A/G]GATTGAAGCCCTGAT | 317 |
rs367694884 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681153 | TGCAATCTCTGCCTC[C/T]AGGATTCAATTGATT | 317 |
rs367695748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660897 | ATATCAGAATATAGG[A/G]TGAGAAGAGTATTTT | 317 |
rs367695845 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710201 | TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGAGATG | 317 |
rs367737265 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682052 | ATGATTAATTTTTTT[-/G]TTTTTTTTTTTTTTT | 317 |
rs367767619 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652814 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 317 |
rs367782321 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645319 | AGAGGTAGCGAGTGG[A/G]CGTGACTGCTCTATC | 317 |
rs367796414 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685594 | CTGCCTCAGCCTCCC[A/G]AAGTGCTAGGATTAC | 317 |
rs367861545 | snp | A/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647029 | AAGAAGTCTCTTAAT[A/T]TTAGGACTTCAATGT | 317 |
rs367870018 | snp | A/G | 6.59707e-05 | 0.00574291 | intron-variant | APAF1 | GRCh38.p7 | 12:98659367 | GGTCAAATTTAGTTG[A/G]TGTGTCAGGTCCCAT | 317 |
rs367920751 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709550 | CAGAGATGTCCTGGA[A/C]GTGGTGATAGCGTTG | 317 |
rs367942061 | snp | A/G | 3.29875e-05 | 0.00406112 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715475 | TCCAGGTTTCAGCAC[A/G]AGAAAACTGTATGGC | 317 |
rs367942215 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690014 | TCATAGTACAGAATT[A/G]TACTCAAGTATTCAG | 317 |
rs368006226 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691764 | CCTCATTTTACATCA[A/G]TGTTTTATTCTTTCT | 317 |
rs368037586 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704944 | ACCAGCATGCCCGGC[C/T]AATTTTTTTTTGTAT | 317 |
rs368109498 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98698260 | GTCTCACTGTGTTGC[A/C]CAGGCTGGTCTTGAA | 317 |
rs368133650 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733133 | TTTAGCAGGCCCCCC[A/C]ACCTTTTTTTTTTGT | 317 |
rs368137126 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732384 | TCACACAGTGTAATT[A/G]CCAATCTAATGAGAA | 317 |
rs368174559 | snp | A/G | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648417 | GCTCTGGAAAAGGAC[A/G]TCAAGACATCCTACA | 317 |
rs368216528 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705279 | GGGACTCAGCTCTGG[A/C]GGCTCTGAGTGACAA | 317 |
rs368222332 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707693 | CATTATGCAAAGTAC[-/TA]TATATATATATATAT | 317 |
rs368267229 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | APAF1 | GRCh38.p7 | 12:98675415 | AACTTATCTGTTCTT[C/T]TAGTTGTCATCACTC | 317 |
rs368374940 | snp | A/G | 3.33578e-05 | 0.00408384 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699419 | AAAGCTTTGGGATGC[A/G]ACATCAGCAAATGAG | 317 |
rs368427585 | in-del | -/A | 0.445724 | 0.155538 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665278 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 317 |
rs368429786 | snp | C/T | 0.000609761 | 0.0174502 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666295 | AATGGAAAGTCGTTT[C/T]GTTATTATTTACATG | 317 |
rs368434348 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654214 | TCAGATGGTCATTTG[A/G]TCTGTTTGCCTTTTT | 317 |
rs368437914 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676557 | AATATCTATACTGGT[A/G]GAATAGTTGATATTC | 317 |
rs368448895 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714626 | TGAGATCGTTCATCC[C/T]GCTCATTTAGGAAGG | 317 |
rs368450225 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672475 | TGGCCTTCTGTGAAG[A/G]TGTAAATGAGATAAT | 317 |
rs368465361 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714364 | AGTGGCAGTTTCATA[C/T]GGTGTAGCCTCATAT | 317 |
rs368507199 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702083 | ACATTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 317 |
rs368539451 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684834 | CAGGAAAAAACCTCT[G/T]CCATGTGGGAGGGGG | 317 |
rs368564782 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691207 | CGAGACTCCGTCTTG[-/A]AAAAAAAAGAAAAAA | 317 |
rs368589663 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | APAF1 | GRCh38.p7 | 12:98727217 | TCATTTGTGTGCTCC[A/G]CTTTCAGAAGAAGGA | 317 |
rs368597507 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666195 | CAATTCCTAGGTGTT[A/G]TGTATTCTCTGGGAC | 317 |
rs368645870 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712058 | TGTGTCTCAGGTGGC[A/G]GGCGCAGCAGCTGCT | 317 |
rs368679479 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730703 | CATGTTAATGAGACT[A/G]TCCAAAAGCACAGAG | 317 |
rs368720372 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702835 | AACAAGAGCAGAAGT[C/T]TGTCTCAAAAAAAAA | 317 |
rs368744142 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659336 | CTGATGCTTCGCAAA[C/T]ACCCAAGGTACCGAT | 317 |
rs368761323 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679476 | TCAGCGTACCACATT[C/G]TTCCTGGTTGTAGGA | 317 |
rs368800260 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731883 | CAGTATTTGTTTAGT[A/G]AATAAATAATATAGA | 317 |
rs368863812 | snp | C/T | 0.00015299 | 0.00874479 | intron-variant | APAF1 | GRCh38.p7 | 12:98662652 | CCAAATTACTTACTT[C/T]GTCTTGTGATTTTTG | 317 |
rs368892228 | snp | C/T | 6.67501e-05 | 0.00577673 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735610 | CTGATGGTTCCTGCC[C/T]GGTATGGCTGGCATG | 317 |
rs368955909 | snp | C/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646943 | GACCTAGAGCTGACA[C/T]CCTCCTTGAACGAGA | 317 |
rs369045067 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98673958 | CTGAGAGAATTAAAA[-/T]TTTTTTTTTAAGTTA | 317 |
rs369052697 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725354 | TGGCTGAATAGCAAT[C/G]AAGGCAGATGCTTAT | 317 |
rs369089258 | snp | A/G | 0.0006094 | 0.017445 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677506 | TGCCTGCTTTTCTGA[A/G]GATGGTCAGAGAATA | 317 |
rs369100773 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715650 | TATTTTAAACACATT[A/G]CGTTGGGCATACATT | 317 |
rs369123286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661569 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 317 |
rs369129559 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98682198 | AGCTGGGACTACAGG[C/T]GGCCGCCACCGCGCC | 317 |
rs369134711 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700918 | GTTCATTCATGTTGT[A/T]GCATGTATCAGAACT | 317 |
rs369195693 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652073 | ACCCACCTTGGCCTC[C/G]CAAAGTGCTGGAATT | 317 |
rs369243616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678123 | TTTAGTCTTTGCAAG[A/T]TTATGACTCCATAGC | 317 |
rs369329547 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675607 | ACAACTGTTTACATA[A/G]CATTTACATTGTACT | 317 |
rs369341962 | snp | A/G | 1.6664e-05 | 0.00288647 | intron-variant | APAF1 | GRCh38.p7 | 12:98667692 | GACTTCCCTTTTTCC[A/G]TATGTATTACAAATA | 317 |
rs369367488 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98673018 | CCGCCTCAGCCTCCC[A/G]AAGTGTTGGGATTAC | 317 |
rs369378547 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710953 | CAAATTCAGGAGTAG[A/G]TACTGGGAGTAAATC | 317 |
rs369386500 | snp | G/T | 2.35724e-05 | 0.00343302 | intron-variant | APAF1 | GRCh38.p7 | 12:98683100 | CTCTGTTCTCCCTTT[G/T]AAAATAATGGATATT | 317 |
rs369419996 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | APAF1 | GRCh38.p7 | 12:98648614 | TATACTAAACTACTT[A/C]ATTTTTTTTAGCCCA | 317 |
rs369544125 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667574 | CGCATACTCTTTCAC[C/T]AGATCAGGAAGACTG | 317 |
rs369603958 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714354 | TTACCTATAAAGTGG[C/T]AGTTTCATATGGTGT | 317 |
rs369724283 | in-del | -/ACTGCTTAGTTG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682004 | TGTTATATGGCATAG[-/ACTGCTTAGTTG]TCTTACATAGTAACT | 317 |
rs369724536 | snp | C/T | 2.17012e-05 | 0.00329395 | missense, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732559 | ATATTTTACAGACTT[C/T]AGAATAAAATAGTTA | 317 |
rs369734554 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | APAF1 | GRCh38.p7 | 12:98712504 | TATATGTCTGGCATT[G/T]TGCACTTCTATTTTT | 317 |
rs369751053 | snp | A/C | 1.66421e-05 | 0.00288458 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732497 | GAAAATACACGTGTC[A/C]CCTGACTTCAAAACA | 317 |
rs369766511 | snp | A/G | 1.67228e-05 | 0.00289156 | intron-variant | APAF1 | GRCh38.p7 | 12:98648849 | TTCTATCACTTTGCT[A/G]TCAAAATTGCTTTGG | 317 |
rs369768631 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703400 | TACTAGTGGCCTATT[A/G]GGAGAAATCCACACG | 317 |
rs369800567 | snp | A/C | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646273 | TCATTACTATAAATT[A/C]AGGAACATTTTATGT | 317 |
rs369895498 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98673468 | AAAACAAAAAAAAAA[A/C]CTTGGGTCTGCCTGG | 317 |
rs369909924 | snp | A/T | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662798 | ATAGTATTATAAAAG[A/T]ATGTAAAGGTATGGT | 317 |
rs369924917 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98691369 | TTCTTGGGCCTTCCT[A/G]AGCCTTATAAAGCCA | 317 |
rs369972462 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729109 | AGGGAGGTGGAAGCA[C/T]AAAGGAGAGGAGTGA | 317 |
rs369973575 | snp | C/T | 6.59163e-05 | 0.00574054 | intron-variant | APAF1 | GRCh38.p7 | 12:98667495 | TTCTGGCTTCTGAAA[C/T]GTTTCATTGGGTTGC | 317 |
rs370055386 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645153 | GGCACTTCTACGCGC[G/T]CGGGCATGAGCCGTG | 317 |
rs370056417 | snp | A/C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718436 | GACAAGGTTTCACGA[A/C/T]GTTGGCCAGGCTGGT | 317 |
rs370062165 | snp | A/G | 0.000199296 | 0.00998039 | intron-variant | APAF1 | GRCh38.p7 | 12:98723333 | TTAAAGTATAAATTT[A/G]TTTTTTGAAAAAGTA | 317 |
rs370063590 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661026 | TCCTGCCTCAGCCTC[C/T]TAGTAGCTGGGACTA | 317 |
rs370083452 | snp | C/T | 0.000115614 | 0.0076022 | intron-variant | APAF1 | GRCh38.p7 | 12:98725371 | AGGCAGATGCTTATT[C/T]TGAGTGTTTATAGCA | 317 |
rs370098029 | snp | C/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644421 | ACAGAAGGCCCAGGT[C/T]TGGGAGGTTGGATCA | 317 |
rs370240643 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702032 | GCTACGCTGCCTACC[A/G]TATGTGCATGCTTGC | 317 |
rs370287396 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732934 | TATTTATTACTGTTA[C/T]GCAGGCTGTGCCTCA | 317 |
rs370296466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689829 | TACATATATCTATCT[A/G]TATCTATAGGTAGAA | 317 |
rs370370266 | snp | A/G | 0.000136549 | 0.00826172 | intron-variant | APAF1 | GRCh38.p7 | 12:98708755 | TTGGTTGAATTTTCT[A/G]TTCACGGTTTTTCTT | 317 |
rs370371079 | snp | A/G | 0.000587087 | 0.017123 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644580 | CACGTTCGGGGGTCT[A/G]CCCAGCCCCCGCCTC | 317 |
rs370518109 | multinucleotide-polymorphism | AA/CC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691248 | GTACCTACTGTTCCT[AA/CC]CTTTCCTTCTTTTCC | 317 |
rs370526015 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668664 | GAAGAATCAAAGATG[A/G]CTCCAAGAATCAAAG | 317 |
rs370541343 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707867 | TTCATCAAGAAAGTC[C/T]TCTTGAAATGAAATA | 317 |
rs370544974 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657380 | TCTGGAGTGAAAACC[A/G]ATTTTTTTCTCTATG | 317 |
rs370551857 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644777 | GGCCGCCTTGGCGTT[A/C]GTGGGAACCCTGGGC | 317 |
rs370556186 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663258 | TTGACTTTAAGAAAT[C/T]ATCCTTGACTCACTT | 317 |
rs370556260 | snp | A/G | 5.86803e-05 | 0.00541634 | intron-variant | APAF1 | GRCh38.p7 | 12:98686721 | CAATACTAGTTGTTT[A/G]TTTATCTTTTTTTCT | 317 |
rs370572309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98702275 | TTTCACCATGTTAGC[C/T]AGGATGGTCTCGATC | 317 |
rs370598135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731133 | GCTTTGTGACCTTGC[A/G]CAAGATTGTTTAACT | 317 |
rs370625919 | snp | A/G | 0.000181913 | 0.00953537 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649635 | AATGGCAGGCTGTGG[A/G]AAGTCTGTATTAGCT | 317 |
rs370678679 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675181 | TTTTGGTGTTTACTA[C/T]AGAAAGGTTTAGGTT | 317 |
rs370694077 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714167 | TCTTTACCTTGATGC[A/C]AAGTCAGTACCACAT | 317 |
rs370713452 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723052 | ATGTGGACACCACAG[C/T]CTTCTCTCTTATTCC | 317 |
rs370736160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652464 | TTTGAACATTTCTTC[A/G]TAAGCTTGTTGTTAG | 317 |
rs370766797 | snp | G/T | 0.00270199 | 0.0366564 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735525 | CATCAACCTTTCTAT[G/T]TAGGCTTTATCAGCT | 317 |
rs370767391 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | APAF1 | GRCh38.p7 | 12:98708565 | GAGATGGAATGATAA[C/T]TTCTTTATCTCTTAA | 317 |
rs370857584 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673791 | AGGAGTTCAAAATCT[C/T]GTAGTGAAGAAAGGA | 317 |
rs370903985 | snp | C/G | 1.64746e-05 | 0.00287002 | intron-variant | APAF1 | GRCh38.p7 | 12:98703507 | GTGTAGAGGTGAGTA[C/G]TTGAATTTATTCTGT | 317 |
rs370928764 | snp | C/G/T | 3.29453e-05 | 0.00405854 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659192 | GTGCATTGGGTTTCA[C/G/T]TTGGGAAACAAGACA | 317 |
rs370935331 | snp | C/T | | | upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645059 | CCACGTCGGGCGCGC[C/T]GCCGCTGCCCGAGTC | 317 |
rs370958029 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649353 | ATTGAAGTTAATATG[C/T]TAGCCACATTTTCTT | 317 |
rs370991051 | snp | C/T | 3.59628e-05 | 0.0042403 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735673 | TTTATTCACTTAGTT[C/T]GTTCATGCATTTGTT | 317 |
rs371038672 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689046 | TCTGAAACTCCTGGG[C/T]TCGAGTAGTCTGCCT | 317 |
rs371065242 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98693616 | TGATTCAAACTTACC[A/C]GGCATTTTATAAGTC | 317 |
rs371118366 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666196 | AATTCCTAGGTGTTA[C/T]GTATTCTCTGGGACA | 317 |
rs371145680 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732159 | TTCCTGTCTGCAGCT[C/T]TCAAGCAGGCTGCAT | 317 |
rs371169377 | snp | A/G | 1.99551e-05 | 0.00315866 | intron-variant | APAF1 | GRCh38.p7 | 12:98686708 | ATGTTTCCCCACTCA[A/G]TACTAGTTGTTTATT | 317 |
rs371342736 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664563 | TTTTAAAGAGCCAGG[G/T]TCTTGCTCTGTCACC | 317 |
rs371385003 | snp | A/G | 3.31587e-05 | 0.00407164 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686770 | ATTTGAATCAAAAAG[A/G]ATGTCGAAATACCAT | 317 |
rs371399207 | snp | A/G | 5.2645e-05 | 0.00513027 | intron-variant | APAF1 | GRCh38.p7 | 12:98662425 | CTTAAGATAAGTGTC[A/G]TTAGTGATTAATATT | 317 |
rs371407416 | snp | G/T | 0.000142865 | 0.00845056 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644748 | CAGCTTCTTCACCAG[G/T]GGGAGCAGGACGTGG | 317 |
rs371417225 | snp | C/T | 8.23676e-05 | 0.00641693 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671690 | GGCCAAGCAGGAGGT[C/T]GATAATGGAATGCTT | 317 |
rs371440544 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726625 | GGCAGGGCTGCTTTG[A/G]AAATGTTCATTTTGC | 317 |
rs371449495 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708274 | TGTGGATTGGTATCA[A/G]ACAGTTTGATAACCA | 317 |
rs371542016 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721221 | TGCCTAGTCAGAAAC[C/G]TTCTGTAACAAAAGC | 317 |
rs371567538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718514 | TGGGATTACAGGTGT[A/G]AGCCACCGTGCCCGG | 317 |
rs371572763 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645367 | AACCAGAGGTGGGGA[A/G]TCTGGGCAGTCGGCG | 317 |
rs371581202 | in-del | -/GAGAGAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689436 | CTTTTGTGTGAGGGT[-/GAGAGAGA]GAGAGAGAGAGAGAG | 317 |
rs371593761 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732392 | TGTAATTACCAATCT[A/G]ATGAGAATTTTATTT | 317 |
rs371633206 | snp | C/T | 9.90851e-05 | 0.00703795 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666352 | AAGAATTGCAGCCAG[C/T]TTCAGGTACTTGCAT | 317 |
rs371666925 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655530 | ACTTCCCAGTAGGGG[C/T]GGCCGTAGTATTTTC | 317 |
rs371681667 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696281 | GGGAGGGGAAGTGGG[C/T]GTGTGCAAAGAGATC | 317 |
rs371701080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682343 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGATGA | 317 |
rs371735204 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685256 | CCCAAAGAGAGGAGA[G/T]ATAATATAAACCCCT | 317 |
rs371739358 | in-del | -/TT | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734924 | AACACACATCAGGTT[-/TT]AAAAAGCCTTGAATG | 317 |
rs371757589 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672267 | CCTCCCGGATTCAAA[C/T]GATTCTCCTGCCTCA | 317 |
rs371806363 | in-del | -/TGGC | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98711035 | AGTCACCTCTGAATA[-/TGGC]TGGCTTGCTTTGATT | 317 |
rs371871697 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686757 | AAATAGCTTTGGGAT[C/T]TGAATCAAAAAGAAT | 317 |
rs371897242 | snp | C/T | 6.59055e-05 | 0.00574007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677465 | TCCCGCTTAGTTGTC[C/T]GCCCCCACACAGATG | 317 |
rs372020077 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733203 | GCAGTGGCGCGATCT[C/T]GGCTCACCACAATCG | 317 |
rs372032284 | snp | A/G | 4.94466e-05 | 0.00497201 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699503 | GGATATGGAAGTGAT[A/G]GTGAAGTGTTGTTCG | 317 |
rs372087287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716003 | TTGTGGATATGGAGG[A/C]CTAAACTTACTATAT | 317 |
rs372096318 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | APAF1 | GRCh38.p7 | 12:98648520 | TCTCTGAAGCAGTCC[A/G]CACTTCCTTAAAAAT | 317 |
rs372125027 | snp | G/T | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715535 | CTTATTTCAAGTTCT[G/T]ATGATGCTGAAATTC | 317 |
rs372134117 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659771 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAAAGAAA | 317 |
rs372152700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98650103 | TCAGTTCTAGGCTGC[C/T]CCCATTCATCAGTGT | 317 |
rs372154070 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700151 | TGGTATTTGTGGTAT[G/T]CAGAGTGCCCTCACA | 317 |
rs372221659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98675530 | AAGAAGTAGATGGTT[A/T]TGTTTGTATTGAACA | 317 |
rs372234984 | snp | C/T | 3.29658e-05 | 0.00405978 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686803 | TTGGTCATACAAATT[C/T]AGTCAATCACTGCAG | 317 |
rs372243253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660720 | GCTGCAAGTACAAAG[A/G]TAAATAAAGCATTCC | 317 |
rs372259373 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648468 | GATGGATTTTTAACA[A/G]TATCAGAAGAGGAAA | 317 |
rs372261485 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645241 | GCATAAGCGGGCGCG[A/C]GCCGTCCGGGCTGGG | 317 |
rs372400613 | snp | A/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671556 | GCAGTCAGTGAGAAT[A/T]TTCAGGAGTTTTTAT | 317 |
rs372424286 | snp | A/G | 4.94572e-05 | 0.00497254 | intron-variant | APAF1 | GRCh38.p7 | 12:98659349 | AACACCCAAGGTACC[A/G]ATGGTCAAATTTAGT | 317 |
rs372493723 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646399 | TGTAAGCCTTGACAA[A/G]CATAGGCAAATGCCC | 317 |
rs372498851 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683601 | GTGGCAGAAAATGTG[A/G]CTACCTTACAGCTCA | 317 |
rs372549328 | in-del | -/TTTTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688774 | TACCACTCTTTTCTT[-/TTTTC]TTTTCTTTTCTTTTC | 317 |
rs372682086 | snp | A/G/T | 4.95334e-05 | 0.00497641 | intron-variant | APAF1 | GRCh38.p7 | 12:98725380 | CTTATTTTGAGTGTT[A/G/T]ATAGCATTGCTAAAC | 317 |
rs372696815 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699833 | GTATGAACTAACATA[C/T]TCAGGGCCCCAGGAA | 317 |
rs372738633 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680351 | GCTTTGTTGTGCATT[C/T]TCTACAGATGACAGA | 317 |
rs372767312 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710225 | AGAGATGAAACTATT[C/T]TCTCATAGTATATTT | 317 |
rs372790619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720002 | GAAACTTACTTGTTA[C/T]AGGCTCCCATGACAC | 317 |
rs372848277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98654706 | GCTGCTGTGCCTGGC[C/T]GATTTTTACAAATTT | 317 |
rs372861046 | snp | C/T | 0.000118148 | 0.00768507 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732515 | TGACTTCAAAACATA[C/T]GTGACTGTGGATAAT | 317 |
rs372899482 | snp | A/C | 0.000412143 | 0.0143493 | intron-variant | APAF1 | GRCh38.p7 | 12:98677587 | AAAATGCAAAGAGGC[A/C]TGTATCCAGTTTTGT | 317 |
rs372956336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684466 | TCTCTCCTCCTCCCT[C/T]TCTTCTTCTGTCTCC | 317 |
rs372956757 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654279 | TTTAAATGCCCTAAA[G/T]TTTTAGTTATACATT | 317 |
rs373020287 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696684 | GTTTGTTTTTAGAGA[C/T]GGGGTTTCACCATGT | 317 |
rs373026616 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672864 | GGTTCAAGCCATTCT[C/T]CTGCCTCAGCCTCCC | 317 |
rs373031668 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644429 | CCCAGGTCTGGGAGG[C/T]TGGATCACCTCCGGC | 317 |
rs373035647 | snp | A/G | 0.00107041 | 0.0231097 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648397 | GTTTGCTTCAACATA[A/G]AGAAGCTCTGGAAAA | 317 |
rs373040331 | snp | A/C/T | 3.30038e-05 | 0.00406212 | stop-gained, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648703 | CTACGTATCATTCTA[A/C/T]AATGCTCTACTACAT | 317 |
rs373043585 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98691383 | TGAGCCTTATAAAGC[A/C]AAAAAGTGAAAAACC | 317 |
rs373043911 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693878 | CTAAGAAAGAATCTA[A/T]GGGAAGTAAATTTTT | 317 |
rs373051639 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688545 | GGTACCATCATGGCT[C/T]ACTGCAGCCTTCACT | 317 |
rs373209321 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667586 | CACCAGATCAGGAAG[A/G]CTGTATGTATTGGTA | 317 |
rs373241517 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667662 | AAGATGACCCATTTA[A/C]AAATTCTTTTATCTG | 317 |
rs373313449 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659402 | CAATAAGATGTAACT[A/G]CTGACCTCTTGAGAA | 317 |
rs373420202 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652457 | ACTCAAGTTTGAACA[C/T]TTCTTCATAAGCTTG | 317 |
rs373421982 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652125 | TGGTGTGTTTTTAAA[A/C]ATTTTTTTGTAGAGA | 317 |
rs373431163 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692513 | TGGTCCTGTCATCCA[G/T]ATAGCATAGTACCCA | 317 |
rs373444324 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721779 | CTTGTTGGGGAGGAC[G/T]ACTGCTAAATGTGGT | 317 |
rs373491125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649891 | AGCAGGAGTTTGGAG[A/G]AAGAATAAAAGTTAG | 317 |
rs373503667 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707009 | GCTGCCCAAGTTCAG[A/G]ACTTTGTTAACTGTT | 317 |
rs373523168 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680000 | AAACTTGGGCAAAGG[C/T]GCCACCGGCCACAGA | 317 |
rs373535568 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697635 | ACAGACACTACTGCA[C/G]TCTTGGTGAGAACTG | 317 |
rs373558323 | snp | C/T | 4.96841e-05 | 0.00498393 | intron-variant | APAF1 | GRCh38.p7 | 12:98708577 | TAATTTCTTTATCTC[C/T]TAATCAGCTCTGGGA | 317 |
rs373618689 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686288 | CATTTGTCCCATGGA[A/G]TGTGCCATATTTTGG | 317 |
rs373647874 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645261 | TCCGGGCTGGGTGGA[G/T]CCGGCGGGATTTGAC | 317 |
rs373666945 | in-del | -/TAGT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723495 | GAGCATTTATACTGT[-/TAGT]CACATTTAAAGTAAA | 317 |
rs373697884 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699143 | CAACATGTAATTTTT[A/C]GCTTCCACACCATGC | 317 |
rs373705811 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708484 | ATTGAAACCTTTCTA[A/G]CATCATAGGTATTTT | 317 |
rs373708723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647357 | CTAAACGTCTATATA[C/T]ATTCATATGATACCA | 317 |
rs373741328 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98670729 | TATTTTTATTTTCTA[A/G]TATTTTTAAATGTTT | 317 |
rs373749980 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690003 | TTCTTTGTAACTCAT[A/G]GTACAGAATTGTACT | 317 |
rs373753930 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709533 | AGGTGTCGTTGCATT[A/G]ACAGAGATGTCCTGG | 317 |
rs373754920 | snp | A/C/T | 0.00013181 | 0.0081172 | intron-variant | APAF1 | GRCh38.p7 | 12:98706621 | TCAGGGTGAGAAATA[A/C/T]TGAGATTTTCATTTT | 317 |
rs373804535 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98728709 | GCCTGGGCAACAGAG[C/T]GAGACTATCTCAAAA | 317 |
rs373823709 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730080 | TGTACCCCCAAAATA[C/T]GTACAACTTAATTAT | 317 |
rs373829999 | in-del | -/TTTAA/TTTAAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724734 | CTAACTGTTCGTGAG[-/TTTAA/TTTAAT]CCTGTCTTTGTGATT | 317 |
rs373865610 | snp | C/T | 0.000164853 | 0.00907741 | intron-variant | APAF1 | GRCh38.p7 | 12:98666164 | TGTACTTTTGTGGCA[C/T]ATTAAATACTTACAA | 317 |
rs373875367 | snp | C/T | 5.09057e-05 | 0.00504482 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665540 | GCATAGTGACTTCAT[C/T]TTTTTTTTAAAGGCT | 317 |
rs373998929 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683081 | AATGGACATTGCTTT[C/G]CCCCTCTGTTCTCCC | 317 |
rs374004436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717067 | TAGAGATGAGATTCC[A/G]CCATGCTGGCCAGGC | 317 |
rs374060808 | in-del | -/AT | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734223 | TCCCTTGTCTCTCTC[-/AT]CCTCTTTTCCTTCCT | 317 |
rs374092603 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675230 | ATTGAGTTTCTGTTT[C/T]CAATGAAATTATTTA | 317 |
rs374107607 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714230 | GTCTTTTAGATAGTT[C/T]AAAAATAAACTCACA | 317 |
rs374132694 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695353 | CTGCGCCCAATGCCG[-/C]CCCCCCCCCTTTTTT | 317 |
rs374135572 | snp | A/G | 1.79922e-05 | 0.0029993 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735541 | TAGGCTTTATCAGCT[A/G]TATGTAAATTCAATT | 317 |
rs374145554 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701844 | TGTGAGTCTACTCCT[A/G]TTGTTAGGTCTTTTT | 317 |
rs374151657 | snp | C/G | 0.00038117 | 0.0138 | intron-variant | APAF1 | GRCh38.p7 | 12:98727127 | TTTAAAACCAGAGAA[C/G]CTTCTGGATAACTCT | 317 |
rs374162552 | snp | A/T | 5.53643e-05 | 0.00526109 | intron-variant | APAF1 | GRCh38.p7 | 12:98649692 | TTTAGAAGGTAAGTG[A/T]CTTAGTCCATTTCAT | 317 |
rs374193816 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98674141 | GCTGAGACTACAGGC[A/C]CATATTACCATGCCT | 317 |
rs374226856 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98703942 | ATAGGATGTTCATTG[C/G]CAGGCACTAATGAAT | 317 |
rs374336587 | snp | A/C | 0.000582094 | 0.0170502 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644581 | ACGTTCGGGGGTCTG[A/C]CCAGCCCCCGCCTCC | 317 |
rs374349572 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649822 | GGAAGGATATGTTAA[C/T]TCTCTGAAGGGAGGG | 317 |
rs374367664 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684508 | CCTCCTCCTCCCCCC[-/A]CCCCCCCTCTCATTC | 317 |
rs374477567 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98702305 | CTCCTGACCTCGTGA[A/T]CCACCTGCCTTGGCC | 317 |
rs374478772 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710199 | TTTTTTTTTTTTTTT[G/T]TATTTTTAGTAGAGA | 317 |
rs374500915 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659234 | CTGATGAAACTGCAG[A/G]ATCTTTGCACACGGT | 317 |
rs374556081 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646790 | GGAAAAATTTGCATT[A/G]TATTTGAAATAAAGT | 317 |
rs374560085 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703406 | TGGCCTATTGGGAGA[A/G]ATCCACACGGGCCAT | 317 |
rs374585670 | snp | A/C | 0.000157988 | 0.00888644 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644745 | GGGCAGCTTCTTCAC[A/C]AGGGGGAGCAGGACG | 317 |
rs374594822 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722446 | ATTAAATAAGTTAAT[C/T]TGAAGTCAAGTATTA | 317 |
rs374616782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98722581 | TATGCATATTTTGTG[C/T]TAGTTACTCATGTTA | 317 |
rs374617395 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709174 | CATACTGAAGTACAC[C/T]TGTTCATTTACACAC | 317 |
rs374653081 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | APAF1 | GRCh38.p7 | 12:98671726 | GGAATGGATGTAAGT[A/T]GGTTAGGAGAGAAAC | 317 |
rs374689156 | in-del | -/ATA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649033 | ACTGCTGAGATAATA[-/ATA]TGTCTACCCTAATTT | 317 |
rs374848524 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728116 | GTGACAGTGGCAGGG[A/G]TGCCCTCAATCCAGA | 317 |
rs374851226 | snp | C/T | 8.24872e-05 | 0.00642159 | intron-variant | APAF1 | GRCh38.p7 | 12:98723153 | CCAATGAGATAGGAT[C/T]GGGGGAGGATTATAA | 317 |
rs374857536 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | APAF1 | GRCh38.p7 | 12:98654974 | AGGCAGAGGACCCTG[C/T]GGCCTTCCGCAGTGT | 317 |
rs374919923 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653235 | GGATTTTTGACATTT[A/C/G]ATTGTATTGCAAAAC | 317 |
rs374978814 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700772 | AAGTAATAACTCCTC[C/T]TTCCCCTCTCTTGCT | 317 |
rs374989716 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672948 | TTTTTAGTAGAGACA[G/T]GGTTTCTCCATGTTG | 317 |
rs374998401 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666291 | TCGGAATGGAAAGTC[A/G]TTTCGTTATTATTTA | 317 |
rs375036035 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666545 | CATTGATACAATACT[C/G]TTCACTAACCTACGT | 317 |
rs375102770 | snp | A/G | 1.65241e-05 | 0.00287433 | intron-variant | APAF1 | GRCh38.p7 | 12:98648500 | AGTAAGAAATGAGGT[A/G]AAGCTCTCTGAAGCA | 317 |
rs375105315 | snp | A/G | 3.44691e-05 | 0.00415131 | intron-variant | APAF1 | GRCh38.p7 | 12:98699404 | TTATTACTTTAATTC[A/G]AAGCTTTGGGATGCG | 317 |
rs375126374 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682454 | TACAGCTTGCAGGGT[A/T]AAGTGTCGATCCCGT | 317 |
rs375182344 | snp | A/G | 6.59044e-05 | 0.00574002 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677466 | CCCGCTTAGTTGTCC[A/G]CCCCCACACAGATGC | 317 |
rs375195806 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98674463 | TCTCTCTCTCTCTCT[C/G]AGAAGCAGCCCCCTA | 317 |
rs375198023 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721382 | GGCAAAGCTAGAATA[A/G]GCAGTGTCTGTAAAC | 317 |
rs375207439 | snp | A/C/T | 6.59243e-05 | 0.00574094 | stop-gained, missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699517 | TAGTGAAGTGTTGTT[A/C/T]GTGGTCTGCTGATGG | 317 |
rs375216001 | snp | A/T | 1.6571e-05 | 0.0028784 | intron-variant | APAF1 | GRCh38.p7 | 12:98727333 | TAAGAGTTCCCCAAG[A/T]ACTGTGAAAGAAAAT | 317 |
rs375253607 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698885 | CCAGTTAGTTTTGTA[A/G]CCCTATCTGGCCCTG | 317 |
rs375268504 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723510 | TAGTCACATTTAAAG[G/T]AAAGGGGTCAGAACA | 317 |
rs375291730 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98719808 | GCTTTAGAAGTGAAG[C/G]ATAGAATGCATATGT | 317 |
rs375350272 | snp | A/C | 0.0146672 | 0.084371 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644856 | TTCCCTCTCCCCGGC[A/C]TCCTCGTTGCTTCAC | 317 |
rs375368528 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684033 | TTTTTTTGAATTGTT[C/T]TTTGGTTTGATTTCA | 317 |
rs375378839 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720831 | AATTAGCCAGGCGTG[A/G]TGACAGGCACCTGTA | 317 |
rs375402599 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677995 | AGAATTTCCTTTAAG[A/T]TTCCCTTTGTTTTCA | 317 |
rs375449857 | snp | A/G | 5.59613e-05 | 0.00528938 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732542 | TAATCTTGGTATTTT[A/G]TATATTTTACAGACT | 317 |
rs375497407 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683204 | ACTCAGAGCAAGTCA[A/G]TTGCTGCCATTTCAC | 317 |
rs375523422 | snp | A/T | | | upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645099 | TGGGAACGCGGCGCG[A/T]CCCTGAGGCTTAGCC | 317 |
rs375547104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679960 | TCAGGCCAAGTGGGT[C/G]AAACAAGACCAGTGG | 317 |
rs375551840 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699638 | TGTTCATTTTTGCAT[C/T]TTACAATGTTTATTC | 317 |
rs375577690 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667063 | TCTGCCAGGTTTCTG[C/T]ACTGTAAAGTCATTA | 317 |
rs375590239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705276 | GTAGGGACTCAGCTC[G/T]GGAGGCTCTGAGTGA | 317 |
rs375602833 | snp | A/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733452 | CTTCTCTTTTAATGG[A/T]GACAGGGTCTTGCAC | 317 |
rs375652538 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660863 | TATGGCAGTGATTCT[C/T]AAATTGGTAAGGGTA | 317 |
rs375666487 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | APAF1 | GRCh38.p7 | 12:98659363 | CGATGGTCAAATTTA[G/T]TTGGTGTGTCAGGTC | 317 |
rs375699480 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98714527 | TTTCATAAAATCAGT[A/C]AGTGGCAGAGCTAGG | 317 |
rs375756272 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719498 | GGGACTACAGGCCCG[C/T]GCCACCATTTCCGGC | 317 |
rs375777430 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646555 | ATTCACATTCCCACT[A/C/T]TCTCTCTCTTTTTCT | 317 |
rs375797968 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706048 | CAGATATCTATATGC[A/G]TATATATCCATACCT | 317 |
rs375812429 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721052 | TTCTACAAGTATATA[C/T]ACATTGCAAAAATAG | 317 |
rs375966404 | snp | A/G | 0.000162253 | 0.00900556 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732570 | ACTTTAGAATAAAAT[A/G]GTTAAGCATTAATGT | 317 |
rs376015106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718115 | CTACCCTCAGTTGTG[C/T]TGGTGCCCTTAAATT | 317 |
rs376065572 | snp | A/G | 4.98782e-05 | 0.00499366 | intron-variant | APAF1 | GRCh38.p7 | 12:98665807 | GTAATGGGATCAATG[A/G]TCCTCATCATTGGGT | 317 |
rs376079372 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693975 | TATGAATTCTGGATA[C/T]TAGACCTTTGTTGGA | 317 |
rs376175905 | snp | A/T | 4.94417e-05 | 0.00497176 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671565 | GAGAATTTTCAGGAG[A/T]TTTTATCTTTAAATG | 317 |
rs376183842 | in-del | -/TACTGTGCTAAGCACTAGCATTTGAGTTTCTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673701 | GCGTTTGAGTTTCTG[lengthTooLong]TACTGTGCTAAGCAC | 317 |
rs376318016 | in-del | -/TT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665279 | ATATATATATATATA[-/TT]TTTTTTTTTTTTTGT | 317 |
rs376335743 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673885 | ATAGAACTGATAAGT[A/T]TTTGGCTTGGAAAAA | 317 |
rs376341920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692829 | GTGTCTTTGCTGTTA[C/T]GAATAGTGCTGCAGT | 317 |
rs376345086 | snp | C/T | 6.59076e-05 | 0.00574016 | intron-variant | APAF1 | GRCh38.p7 | 12:98667502 | TTCTGAAACGTTTCA[C/T]TGGGTTGCAGGATCT | 317 |
rs376371060 | in-del | -/ATAT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665256 | TGCTTAGACTGGCGC[-/ATAT]ATATATATATATATA | 317 |
rs376383317 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672285 | TTCTCCTGCCTCAGC[C/T]TCCAAAGTAGCTGGG | 317 |
rs376396556 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709599 | GAAAGCAGATGCCTC[A/C]TGGAAGATTAAAACA | 317 |
rs376407178 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728917 | TTTTGATGTATCTTT[C/T]ATCTATCCACTCAAA | 317 |
rs376462245 | snp | A/T | 1.71555e-05 | 0.00292873 | intron-variant | APAF1 | GRCh38.p7 | 12:98662632 | ACATTTAAATATGTG[A/T]CATACCAAATTACTT | 317 |
rs376465399 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98716063 | GTCCCAATGCACATT[C/G]TTTTAAAATTCAAAT | 317 |
rs376489741 | snp | C/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646915 | CTTTGTGGGAAATGT[C/G]TTTAGCAAGGAGGAC | 317 |
rs376492610 | in-del | -/TCA | | | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735514 | AAGCTAAATACATCA[-/TCA]ACCTTTCTATTTAGG | 317 |
rs376494061 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667890 | ATCCTCCCACTTCAG[C/G]CCCCCATGTAGCTGG | 317 |
rs376505007 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98687340 | CCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 317 |
rs376525749 | snp | C/G/T | 0.00213746 | 0.0326301 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644555 | CGTCCCCAGCGACAG[C/G/T]AGGCTCAGGCACGTT | 317 |
rs376555132 | in-del | -/AAAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727591 | ATGAGTTTAGTAACT[-/AAAGA]AAAGAACAGAAAAAA | 317 |
rs376597105 | snp | C/T | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648714 | TCTACAATGCTCTAC[C/T]ACATGAAGGATATAA | 317 |
rs376598281 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713957 | GCTTTGTTTTCTCTT[A/T]ATTATTGTGAAAAAT | 317 |
rs376626592 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710861 | GAATAAATTGTATCA[C/T]GTCTTTGAGCCTCAG | 317 |
rs376632932 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | APAF1 | GRCh38.p7 | 12:98647947 | GTGCTGGGATTATAG[G/T]CTTGAGCTACCACAC | 317 |
rs376687206 | snp | A/G | 8.24069e-05 | 0.00641846 | intron-variant | APAF1 | GRCh38.p7 | 12:98667491 | TTGTTTCTGGCTTCT[A/G]AAACGTTTCATTGGG | 317 |
rs376693352 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732901 | ATTTGGAAGAAATTG[G/T]TATTTTAATACTGTC | 317 |
rs376707970 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652148 | TGTAGAGACAGGTTT[C/T]TGCTATCTTGTCCAG | 317 |
rs376709239 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706937 | ATCCAATTACTTGCC[A/G]ATTCTGAGAGAGTCT | 317 |
rs376721744 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98664233 | CATCTTGGCCAGGGT[A/G]GTCTTGAACTCCTGA | 317 |
rs376748797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700369 | ATGAGGGATATTACT[G/T]TTTTAAAGAGCATAA | 317 |
rs376806366 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666333 | AGTAGATTTTCTTAC[A/G]GAGAAGAATTGCAGC | 317 |
rs376917041 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98649738 | ATAGACATGTAAAAA[-/T]ATTATGATATATCAA | 317 |
rs376958146 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683169 | TATGACTGGGGAACT[A/G]GTACACACCTATGAT | 317 |
rs377007489 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728447 | AATTAGTGCCGGGTG[C/T]GGTGACTCACACCTG | 317 |
rs377046554 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693724 | CCAGCTGCCATCCTG[A/T]GGTCTTCCTTACCAT | 317 |
rs377151147 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689401 | TATTTTTTAATGCCC[A/G]TCAAAACTTTAGGCA | 317 |
rs377160893 | in-del | -/CTTTCCTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724316 | ACCCTGAAGAGCATG[-/CTTTCCTC]CTCCTCCACTGGTGA | 317 |
rs377171914 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649616 | GATGGGTCACCATAC[A/G]TGGAATGGCAGGCTG | 317 |
rs377292966 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731499 | TTCTGGAAAATCCCA[A/G]GTTAGTGCATGCTGG | 317 |
rs377310524 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672799 | CACTCTTGTCGCCCA[C/G]GCTGGAGTGCAATGG | 317 |
rs377316633 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98710373 | CTTATGCCATCTTTT[C/T]GTTTGATTTTTCTTG | 317 |
rs377376484 | snp | A/G | 0.00318876 | 0.0398022 | intron-variant | APAF1 | GRCh38.p7 | 12:98699365 | TAGAAGTGTGATTAT[A/G]GAGTAAAACAAACTT | 317 |
rs377421920 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701736 | CCATGCTAAAAGAAA[C/G]CTACCCAAAGGTGTT | 317 |
rs377459800 | in-del | -/AAGAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727597 | TTAGTAACTAAAGAA[-/AAGAA]CAGAAAAAAATATTG | 317 |
rs377478232 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682266 | CACCATGTTAGCCAG[G/T]ATGGTGTTGATCTCC | 317 |
rs377482193 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687694 | ATGACCTAATCACTT[C/T]TGAAGGTCCCATCTC | 317 |
rs377484625 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707778 | AGGCAGAGAAAGACT[A/G]AGAAAGGTCATTGGT | 317 |
rs377486420 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679250 | CCACTCTAGTGCCCC[C/G]TCTTTGCTGAGAGCT | 317 |
rs377532286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701453 | CAGCTGCACCGTTTT[A/G]CATTCCACTAGCAAT | 317 |
rs377621175 | snp | A/G | 4.94319e-05 | 0.00497127 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703415 | GGGAGAAATCCACAC[A/G]GGCCATCACAGCACC | 317 |
rs377621845 | snp | C/T | 6.68014e-05 | 0.00577895 | intron-variant | APAF1 | GRCh38.p7 | 12:98649452 | AATTATTCCAAAGTT[C/T]TATTCATTCATGCTT | 317 |
rs377641177 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702530 | TATAAATCTTAAAAA[C/T]TGAAGAAACTGCGGC | 317 |
rs377650542 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98683284 | CTCAAAGTAAGTGTG[A/G]ATATTGAGAATTAGG | 317 |
rs377713202 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668073 | ACAGGCATGAGCCAC[C/T]GCGGCTGGCTGAAGA | 317 |
rs377727906 | snp | A/C/T | 4.94262e-05 | 0.00497098 | intron-variant | APAF1 | GRCh38.p7 | 12:98683315 | TAGATAAATTTGATT[A/C/T]GTACATCAGAGTATC | 317 |
rs386377532 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674449 | GGAGGTCTCTCTCTC[-/CT]TCTCTCTCTCTCTGA | 317 |
rs386765652 | multinucleotide-polymorphism | CAG/TGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661091 | TATTTTTAGTAGAGA[CAG/TGA]GGTTTCACCGTGTTA | 317 |
rs386765653 | multinucleotide-polymorphism | AA/GG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667196 | TAAACTCCTGGGCTC[AA/GG]TTGGTCCTGAGTAGC | 317 |
rs386765654 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718325 | GAAACCTCCACCTCC[AAA/GAG]GTTCAAGTGATTCTT | 317 |
rs386765655 | in-del | CCTG/TTTAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724735 | CTAACTGTTCGTGAG[CCTG/TTTAA]TCTTTGTGATTAAAC | 317 |
rs386765656 | multinucleotide-polymorphism | AT/TC | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734223 | TCCCTTGTCTCTCTC[AT/TC]CCTCTTTTCCTTCCT | 317 |
rs397744805 | in-del | -/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98676664 | GTTTTTTTTTTTTTT[-/T]GAAATGGAGTCTTGC | 317 |
rs397952983 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673456 | CAAAAAAAAAAAAAA[-/A]CAAAAAAAAAACCTT | 317 |
rs397955270 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707712 | ATATATATATATATA[-/TA]CATATAAATTTACTA | 317 |
rs397975606 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723635 | TTTTTTTTTTTTTTT[-/T]AAGGTATGGAATATT | 317 |
rs398020795 | in-del | -/A | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98647725 | ATAATACTGTTGCTG[-/A]AAAAAAAAAAAAAAA | 317 |
rs398020798 | in-del | -/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733920 | TTAGGAAAGATCAGG[-/T]TTCATTCAAGTAAGA | 317 |
rs398044705 | in-del | -/A | 0.5 | 0 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730821 | ATTGAGTGCCAGTAA[-/A]GATAAAGTAGGTATC | 317 |
rs527254951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661195 | CGTGAGCCACTGCGC[C/T]CGGCCCCTCCTTCTC | 317 |
rs527284806 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683820 | GTCAACTCTACTTGA[A/G]TCGTAAGTAGAGCTT | 317 |
rs527298858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98655705 | TGCAGCCTCAACTTT[A/C]CAGGCTCAGGTCATC | 317 |
rs527314665 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715532 | ACTCTTATTTCAAGT[C/T]CTGATGATGCTGAAA | 317 |
rs527350053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646927 | TGTGTTTAGCAAGGA[C/G]GACCTAGAGCTGACA | 317 |
rs527377325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707791 | CTGAGAAAGGTCATT[A/G]GTTCTTAACATGCCA | 317 |
rs527444688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684722 | AACTTGGCCCTATTT[G/T]AATAAATGTACCACT | 317 |
rs527490620 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712583 | GTACAGTGACACGAT[C/T]ACAGCCGACTGCAGC | 317 |
rs527500977 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98677894 | AAAACAGTGATTAGG[A/C]AAATACCTATTTTAT | 317 |
rs527514366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669175 | TTATCGAACATTTAG[A/G]TTTTCAGTTTTTTTG | 317 |
rs527523574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98729929 | TTGATAATACAGTAG[A/G]GAAATTATAGTTAAC | 317 |
rs527580406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98691201 | GAAGAGCGAGACTCC[A/G]TCTTGAAAAAAAAAG | 317 |
rs527602042 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98715104 | GGAGGGCAAGCCCAG[A/C]CAGCCACTTGTTTGA | 317 |
rs527641331 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98679295 | AGGACCAGCTGCAGA[C/G]AGGAGCTACCCTCTC | 317 |
rs527656837 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726087 | CCTAATTGAGTCACA[G/T]TCTGCATGCTAGGCC | 317 |
rs527659985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98694785 | CTTTGCTATCTGCTC[A/G]TATTTAAGAATACAT | 317 |
rs527693812 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722305 | CTATCATTGTATCTT[-/C]TATTGTAGGACTTTT | 317 |
rs527708627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672081 | CTGTGACTTTGAACA[A/G]GTTACAGGTTTTTCT | 317 |
rs527716851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724348 | TGGTGAACTGTCCCA[G/T]CATCCTGCCTCTGGT | 317 |
rs527747561 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722905 | CTGGCATATTGTGTG[-/T]TTTTTTTTTTTCTAT | 317 |
rs527778835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725038 | TGTCCTCATTTTACA[C/G]ATGCCGTGTCTGAAG | 317 |
rs527785409 | snp | C/T | 1.65682e-05 | 0.00287817 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708646 | AGCAAGAAGTAGATG[C/T]TGTGTTTCAAGAAAA | 317 |
rs527858275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98693618 | ATTCAAACTTACCAG[A/G]CATTTTATAAGTCTT | 317 |
rs527879137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647636 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 317 |
rs527944604 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674934 | TTGAATGAACTCATG[C/T]TTCAGTTAGTGGCTG | 317 |
rs527960225 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694356 | ATGGTGGCTTCTTTC[A/C]ATCTGGAAACTTATC | 317 |
rs528014107 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732146 | TGGACTCTATAGCTT[A/C/T]CTGTCTGCAGCTCTC | 317 |
rs528026175 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98678831 | TGCTGACATGCCAGC[C/T]CCCTGCCGCCTCGGC | 317 |
rs528090281 | in-del | -/TTTA | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98664004 | ACACAGTTTTGTTTG[-/TTTA]TTTATTTATTTATTT | 317 |
rs528145001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728383 | ATTCTTGGTTTACAG[A/T]TGAGGAAAATGATTT | 317 |
rs528188858 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678996 | GTTCCTGGGTGGAAG[C/G]GGGCGGGTCACCAAT | 317 |
rs528232886 | in-del | -/CTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709311 | CTACTCTAGTCTGTT[-/CTC]CTTCTGCCACCCAAC | 317 |
rs528246234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696726 | GTCTTGAACTCCTGG[A/G]CTCAAGTGGTCCGCT | 317 |
rs528254447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651401 | AGGTATTTTAAATTT[A/G]CATAGATGTTATGGT | 317 |
rs528307292 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644114 | TTGCAAGTATTTCCA[C/T]TAGGTATTTATGGGG | 317 |
rs528353606 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734387 | ATTTTCTCTGAAATA[C/T]ATTATTAAGGGCAAT | 317 |
rs528418571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98681923 | GAAATGCCAAAGGAC[A/G]TTAGTACCTCTAAAA | 317 |
rs528420939 | in-del | -/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735349 | ATATAGCTTATATGA[-/T]TTTTTTTGCCTTGGT | 317 |
rs528458271 | snp | C/G | 1.65026e-05 | 0.00287246 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699465 | GTGAAACAGTTCTTC[C/G]TAAATTTGGAGGACC | 317 |
rs528464946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98691086 | GTGGCGCATGCCTGT[A/G]ATCCCAACTACTCAG | 317 |
rs528469291 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645158 | TTCTACGCGCGCGGG[C/T]ATGAGCCGTGGCAGG | 317 |
rs528475375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653735 | ATATAGTTTTTAACT[A/G]TTTATGTCTATACAG | 317 |
rs528518338 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645477 | AGGGCGCCACAGGCC[A/G]GGAAGACCTCCTCCC | 317 |
rs528579696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692114 | TTTAGACAGAGTCTC[A/G]CTCTGTTGCTGAGGC | 317 |
rs528599148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98729325 | TAGGAAGTGGGGAGC[A/G]GGGAATGGTTTCAGG | 317 |
rs528640414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684017 | AGAAAGATCTGCTAA[C/T]TTTTTTTGAATTGTT | 317 |
rs528643561 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651803 | GAGCTGGGTGCACAC[A/G]CCACCATGCCTGGCT | 317 |
rs528681150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98667858 | CTCATTACACCCTCA[C/T]CTCCTGGGCTCAAGT | 317 |
rs528765280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653202 | GAGTTCACTTCCATT[C/T]TCAAATACAGGAACA | 317 |
rs528791411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705950 | TCATCCCTATCCCTT[C/T]GCCTCGCTCTCCCTC | 317 |
rs528870039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694688 | TGAAGTTTTCATATT[C/G]CAGTGTAATAGATAT | 317 |
rs528874204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657484 | GATCCTTTCCTTGAC[C/T]TTGTGCAGGTTCAAA | 317 |
rs528877600 | snp | C/T | 1.65127e-05 | 0.00287334 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648727 | ACTACATGAAGGATA[C/T]AAAGATCTTGCTGCC | 317 |
rs529021285 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675233 | GAGTTTCTGTTTTCA[A/G]TGAAATTATTTATTC | 317 |
rs529037865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1 | GRCh38.p7 | 12:98665150 | TCCTCCCACCTCAGC[C/T]TCCTAAGTAGCCGGC | 317 |
rs529069360 | snp | A/G | 4.97607e-05 | 0.00498777 | intron-variant | APAF1 | GRCh38.p7 | 12:98671757 | CAAAGGGAGTGGTGC[A/G]CTAACTATATCATTA | 317 |
rs529080234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716360 | TTATCCCAATTATAA[C/T]GAAATTTTGTTTAGA | 317 |
rs529107227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663946 | TATAGGCATGAGCTA[C/T]CATACCTGGCCACCT | 317 |
rs529198185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701599 | TTCCCAATTACCAAT[A/G]ATGTTGAACAAAAGA | 317 |
rs529247113 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673256 | GAGGCCGAGGCGGGC[A/G]GATCACCTGAGGTCA | 317 |
rs529315650 | snp | C/T | 0.000214145 | 0.0103454 | intron-variant | APAF1 | GRCh38.p7 | 12:98659152 | TTCATTATTCTTTCC[C/T]TCACTAGGTTGTTTC | 317 |
rs529331747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718752 | CCAGCCTGGGCAACA[C/T]AGCGAGACCCCATCT | 317 |
rs529379367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703727 | TGACAGGGAATTCAG[C/G]AAGCATTTGCTGAAT | 317 |
rs529384805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703041 | AGTATTCATTTTCTC[C/T]TTTGAATAAACAAGC | 317 |
rs529416924 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698553 | TTGGCCATGTTTCTT[A/T]GTATATATAATACTT | 317 |
rs529447142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98679946 | CTGAATGCAGCCTGT[C/T]AGGCCAAGTGGGTGA | 317 |
rs529512852 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98672877 | CTCCTGCCTCAGCCT[A/C]CCGAGTAGCTGGAAT | 317 |
rs529534371 | snp | C/T | 0.000263557 | 0.0114764 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725465 | ATTGAGGGGCCACAA[C/T]GGCTGTGTGCGCTGC | 317 |
rs529554598 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670471 | TTTTCTATAAAAAAT[A/G]ATTTTCTATAAAAAT | 317 |
rs529598243 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704894 | AAGCTATTCTCTTGC[C/T]TTAGCTTTCTGAGTA | 317 |
rs529609081 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731423 | TGACTGAAAACAAAT[C/G]AATCTCAGGTTGGTG | 317 |
rs529625754 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686989 | AGCCTGCTTCTTTCA[A/G]TTTCCAGGAGCATAT | 317 |
rs529631318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718170 | TGTCACTGTCTGTCT[A/G]CTTTCTTCCTTTTTT | 317 |
rs529645049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98711452 | AGATGTTCAGCTCTT[C/T]GTAGTTCAATTTTCA | 317 |
rs529646649 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98669991 | GTTGCCCAGGCTGGA[A/G]TATAGTGGCATGATT | 317 |
rs529683147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714139 | TCTTAAAGAGTCCTT[C/G]GTTTCCCTTTTCTCT | 317 |
rs529696304 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682382 | TACTGAAAACTGAAC[A/G]CTATAAGAGGCTATA | 317 |
rs529721418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654019 | GAGTTTTCCCTGAAT[A/G]AAGGCAACTTTTCTC | 317 |
rs529740738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722482 | GCTCTAAATACAGTT[A/G]CTTTTAGTAATTAAG | 317 |
rs529779336 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656918 | TGATGTAATCACCGT[C/T]TCATTCATTGACGAT | 317 |
rs529801350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98714863 | TTTTTTTTTGACATA[A/G]TCATTATCTTTTGAA | 317 |
rs529865560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692016 | TAAGTAACATACCAT[A/G]CCTCAAAGTTATTGC | 317 |
rs529969095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98729239 | GATACTCTATATCAG[C/T]GGTCCCCAGCCTTTT | 317 |
rs529989722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685923 | ATTACAGGGGTGAGC[C/G]GCCATGTCCAGCCTG | 317 |
rs530029187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721609 | ATTGGGTTCTTAAAA[C/T]ATGAAAATTACTAAT | 317 |
rs530089847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731936 | CAAGGGCTCTTGCAT[A/C]ACACCTGGGGAAAGG | 317 |
rs530123943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678622 | TGTAGCTGCCCAAGC[A/G]GTGGCTGCAGACTCA | 317 |
rs530146709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731267 | TCCATTATGAACATC[C/T]CCCCACCAGAGATGT | 317 |
rs530149610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724036 | AGGCAATAAAAATCA[C/T]TGAAAAGCATTTACA | 317 |
rs530149685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715673 | CATACATTCAGATTA[C/T]GTACATGGGCTTAGA | 317 |
rs530207519 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661744 | AAAGTGCTGGGATTA[C/T]AGGCCTAGAGTATTT | 317 |
rs530286461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663822 | TTCCACCATGCCTAG[C/T]TAATTTTTGTATTTT | 317 |
rs530294159 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98655435 | CCCTCACCTCCCGGA[A/C]GGGGCGGCCGGCCGG | 317 |
rs530365332 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98693578 | TTATCTTCAAACTCT[C/G]TCTTGTTAATTTGCT | 317 |
rs530377171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689361 | CTTTTCTTAGGATGT[C/T]TTTTGCCTTCGATTT | 317 |
rs530394889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98688512 | AGTCTCACTCTTTCA[C/T]TCAGGCTGGAGTGCA | 317 |
rs530475517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98726709 | TTTCATTTTTCAACC[A/G]CTGCAGGAAAAAGTT | 317 |
rs530543991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727797 | AATACAAAAAATAGC[C/T]GGGCGTGGTGGCATA | 317 |
rs530559512 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704052 | GCCCTGGAAGAATTC[C/G]ACCCAGTGAAGTGCT | 317 |
rs530595603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98658380 | TATTGGTAAGTTGCT[C/T]TCAGATCCATAACAC | 317 |
rs530653497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98674408 | ACTTTCCAGAGTTGA[C/T]CATTCCTTAATACTT | 317 |
rs530654088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650510 | GTTTTTTGTTTTTTT[G/T]TTTTTGATATGTATG | 317 |
rs530663930 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98707457 | ATGCCATCTAATTCT[A/G]TGTCATTTTCTAGTG | 317 |
rs530693787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703608 | CTTGCTTGAGAAATT[A/C]TAGAGTATTTTCTTT | 317 |
rs530753667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696646 | CTGTGCTTGAAACTT[A/G]GGAGTGATCTTTTTG | 317 |
rs530783506 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98651297 | CCTTTCCCCTCTCCA[C/T]GGACAATCCTAATGT | 317 |
rs530790260 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98652210 | CTCCCGCCTTGGCCT[C/T]CCAAAGTGCTGGGGT | 317 |
rs530838098 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643992 | GGCTGATTATTCGTA[C/T]TTTTGGTAGAGATGG | 317 |
rs530872659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688678 | AGATAGGATCTTACT[A/G]TGTTGCCCATGCTTG | 317 |
rs530890206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697986 | CCTGGGGTGCACAGG[A/G]ACCCTGGATACAGTG | 317 |
rs530973517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653126 | TATTCTCTGGAGTCT[A/G]CCTTTGTATGTCCAC | 317 |
rs531001681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98698735 | GCAGTCATTATCACT[C/G]TGTGAGGCTGAGACA | 317 |
rs531045703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719511 | CGTGCCACCATTTCC[A/G]GCTAATTTTTTTTTT | 317 |
rs531066880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690911 | TCATAACAGTGTCCA[A/C]AAAGTCCTGTACTTG | 317 |
rs531075805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660183 | AAACCCTGTCTTTCT[A/G]AAAAATACAAAAATT | 317 |
rs531110602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712478 | TCTGTACAGAATTAA[A/G]TAAAACTAATTATAT | 317 |
rs531129107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667239 | TAGTTGGGTCTGCAG[G/T]CATATGCCACCACAC | 317 |
rs531135102 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706952 | AATTCTGAGAGAGTC[A/T]ACCTTTTCATTTTCT | 317 |
rs531139990 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648555 | AGAATTTCAGAACTT[C/G]TACTGGTCTCCACTA | 317 |
rs531220101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656767 | TGACATGGCAACTTT[C/T]TTCCTTTATATCCTA | 317 |
rs531234238 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | APAF1 | GRCh38.p7 | 12:98656812 | AGGAAATGGGTGGGC[A/G]TTGTTCTTGCTCTCT | 317 |
rs531266999 | in-del | -/AA | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98647096 | GTATTTTATTGTAAG[-/AA]ATGATAATGTGTGCT | 317 |
rs531275221 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98648239 | GTTTTGTTCTTTTTA[A/C/T]GTTTCTTGTTTATTA | 317 |
rs531311315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98656314 | AATATATACACATAC[A/G]GAACACAGCTTTAAG | 317 |
rs531413086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701463 | GTTTTACATTCCACT[A/G]GCAATGTACAAGGGT | 317 |
rs531476362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694493 | TGTCCATTTGCCCTA[C/G]TTTTTGAAAGATTTC | 317 |
rs531488001 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733805 | GTCTACCCTTTTCTC[A/G]CTGTAGCTGCTGGCA | 317 |
rs531491800 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664273 | CCACCTGCCTCAGCC[A/T]CCCAAAGTGCTGGGA | 317 |
rs531525601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678579 | CCGGCTCCACAGAGC[A/G]GGCAGGACCCCTTCC | 317 |
rs531533484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98687724 | CTCAATACTTGCATC[A/G]GGGATTAAGTATTTA | 317 |
rs531557355 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98714804 | TTTCCTCTCTTTTTG[-/T]TTTTTTTGGTATGAG | 317 |
rs531575291 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667257 | TATGCCACCACACCT[A/G]ACTGATTTTTTTTAT | 317 |
rs531596999 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98663207 | GCGAAGTTAAACTTT[C/T]TACTTGTTTATTGAA | 317 |
rs531599787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673453 | AAAACAAAAAAAAAA[A/C]AAACAAAAAAAAAAC | 317 |
rs531599884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664906 | TGAAAAAAATTTACC[A/C]GTGGCATAATATTGA | 317 |
rs531614715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98698006 | TGGATACAGTGTAGC[A/G]ACTTGCTCAGAATGA | 317 |
rs531658812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665453 | GCTTTTGATAACATG[A/C]AGCAGAAATTGTTTC | 317 |
rs531709710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718072 | TATGTACACCTTCCC[C/T]TGATCCCTCATTCTC | 317 |
rs531768947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717162 | CATGAGCCCCCGCAC[C/T]TGGCCTACTGTGCTC | 317 |
rs531776753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725896 | TGTAAATTATGGTCT[G/T]GATTATAAATGAATT | 317 |
rs531796491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657751 | ACTTTAAGTTTGAAT[C/T]TCAACTCTGCTTCAT | 317 |
rs531858948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670085 | GAGTAGCTGGGAGCA[C/T]GGGTGTGCACCACCA | 317 |
rs531896427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695014 | GAACTGGTTGGGTGT[C/T]CAGAGTAAAAATTTT | 317 |
rs531920116 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726405 | CAGTGTAGATGAGGA[A/T]GATGGGGTTTTCCCC | 317 |
rs531940943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98676213 | TTCCTTTACACCTTA[C/T]TATTTATTTATTTAT | 317 |
rs531945868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679425 | CTATTTTATCGCTCA[A/G]TAAAGCTCCTGTTTG | 317 |
rs532002892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98677040 | TATTTTAAAAAAGAG[A/T]TGGAGAATTTTTGAA | 317 |
rs532044412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720764 | AGGTCAGGAGATCGA[G/T]ACCATCCTGGCTAAC | 317 |
rs532047525 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695362 | ATGCCGCCCCCCCCC[-/CT]TTTTTTTTTTTTGAG | 317 |
rs532049021 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98664267 | CGTGATCCACCTGCC[-/T]CAGCCACCCAAAGTG | 317 |
rs532105176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713185 | TTCGTTAAACTAACA[A/G]TCATCTTATCCAGTT | 317 |
rs532135552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98682146 | GCAAGCTCCGACTCC[C/T]GGGTTCATGCCATTC | 317 |
rs532138370 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709442 | GAGTGGTGGTAACAG[A/G]TGCCCTAAGAGCAGA | 317 |
rs532145434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661103 | AGATGAGGTTTCACC[A/G]TGTTAACCAGGATGG | 317 |
rs532162168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690129 | AGATTCAGCAATGCT[A/G]CTAACTCCTGAGAAA | 317 |
rs532177769 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98729176 | TGGAGGGGAATGCTT[G/T]AAGTGAGTCTTTTGA | 317 |
rs532203268 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644993 | AACTCCCGGGCGCGC[G/T]CAGGCCGACGGGACC | 317 |
rs532229593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721564 | AAGCCAGAAATGCCT[C/T]CATTTCTTCCCCTTC | 317 |
rs532234227 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653802 | CTTTAATTTTTTCTT[A/G]TTTGTAGGGAAATAG | 317 |
rs532273425 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652189 | AACTCCTGGGCTCAA[C/G]TGATGCTCCCGCCTT | 317 |
rs532319788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683026 | ATCTTGTCCAACTAG[A/G]AAAATCTGCTATGAC | 317 |
rs532475117 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734415 | AATGGAGATAAATTA[A/C]TAGTAGATGTGGTTC | 317 |
rs532491347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692789 | TTTCCTTTAACCTTC[C/T]GTTGATGGGCACCTA | 317 |
rs532528731 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98685848 | TGCTATGGTGGTCAG[G/T]CTGGTCTTGAACTCC | 317 |
rs532535453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98705996 | AAACTATTTTCTGTT[C/T]TTGGCTTAACTGTCC | 317 |
rs532539838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646684 | GAATGAATTGATAAA[C/T]CCGTTTAGACTCTTT | 317 |
rs532555539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684823 | GGAAATAAATACAGG[A/G]AAAAACCTCTGCCAT | 317 |
rs532646069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98706988 | TATCTCTACCTTTCC[A/C]TTTCTGCTGCCCAAG | 317 |
rs532668858 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98654899 | TTTGGCAGGGTCATG[G/T]GACAATAGTGGAGGG | 317 |
rs532683995 | snp | A/G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716015 | AGGCCTAAACTTACT[A/G/T]TATATTCTTTTAAAA | 317 |
rs532736582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692196 | CATGCCATTCTCCTG[C/T]CTCAGCCTCCCTAGT | 317 |
rs532754357 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685136 | TTGCCAAAACTAACA[C/T]TTAGCAATAATTGAT | 317 |
rs532761364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695806 | AGAAGGTACTGGGTG[C/T]CAGCACTTCCTGAGT | 317 |
rs532764984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653932 | CCTATTTGTTTCTGT[C/G]CTTTCCAAGATTTCT | 317 |
rs532822025 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733660 | GCTGGTCTTGAACTC[G/T]TGGCCTCAAGTAATC | 317 |
rs532925113 | snp | G/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730876 | TCCAAATTATTCCTA[G/T]TTATAAGTGAAAAAA | 317 |
rs532976491 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721293 | TCTTTGTTATATCTG[C/T]TCCAGAAGGCTGTCT | 317 |
rs532981119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664807 | CCTGAAGTGCTAGGA[C/G]TACAGACACATGTCG | 317 |
rs533051534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98710270 | GCTCTTGAAGAGCAC[A/G]AATACAGCTTGAGTT | 317 |
rs533067795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98726052 | TTCACATTTCCGTCA[C/T]TGTGGGGCAGCGAAG | 317 |
rs533094584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689200 | TCTAAGGTTCTTCAC[A/C]TTCCGTCATTCTGCC | 317 |
rs533106338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680871 | GAAATCTTTGAGTGC[A/G]TTGTGATTAGGAGTG | 317 |
rs533117429 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647863 | TGATGGACATTTAGG[A/T]TGCGTTCATCACTGA | 317 |
rs533165701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651576 | CAACTCTCTGCTGCT[A/G]CAGCAAAGCTGGGTT | 317 |
rs533171408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657557 | ATTAATATGTCAAGT[C/T]CTATTCAGTACTCCA | 317 |
rs533225438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98652181 | TGGTCTCAAACTCCT[A/G]GGCTCAAGTGATGCT | 317 |
rs533265160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695193 | AAGTAGCTGGGATTA[C/T]AGGCACGCACCACCA | 317 |
rs533308044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697738 | CAGGTAGTAAGCAGA[A/G]GTCCTGCAAAATGAT | 317 |
rs533332408 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98703890 | GTGGTGAGAAATGAG[C/T]CCAGTTCAGATTTCT | 317 |
rs533334479 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | APAF1 | GRCh38.p7 | 12:98712306 | TAACTGATTTTGCCT[C/T]ATTTTTCATTAGCTC | 317 |
rs533372428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660066 | AATGTCAGGAAGGGG[A/C]CAGGGACAGTGGCTC | 317 |
rs533373588 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705715 | CATGAATAACAAGAG[A/C]AATGTGTACATGTTA | 317 |
rs533443069 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98676170 | TCACTGCACTAATAG[-/T]TTTTTTCTGGTTTAA | 317 |
rs533452632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718766 | ATAGCGAGACCCCAT[A/C]TCTGCAAAACAAAAT | 317 |
rs533650610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684304 | ATACAGAAGCTCAGT[A/G]TGTATAAGAGTTAAA | 317 |
rs533659322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692957 | TTAAGTTATTTGAGA[A/C]ATCTCCAAACTGCTT | 317 |
rs533684737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719367 | CTTTTCTTTTCTTTT[C/T]TTTGAGACAGTCTTG | 317 |
rs533749029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679613 | AAAGCTGCGGCCCTT[C/T]GGGGAGCCCAGACTT | 317 |
rs533761458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98661190 | ACAGGCGTGAGCCAC[C/T]GCGCTCGGCCCCTCC | 317 |
rs533815849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699687 | TGTGTGATTTTGGGC[A/G]GTCTTCCTAACCTGT | 317 |
rs533850313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98699232 | TTTTCTTTTTAAGAA[C/T]GTAATAATGAAACTG | 317 |
rs533869365 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98653452 | ATTTGAGGTCAGGAG[A/T]TTGAGACCAGCCTGG | 317 |
rs533902653 | snp | A/G | 5.20052e-05 | 0.00509901 | intron-variant | APAF1 | GRCh38.p7 | 12:98671117 | TGAAAAATTAGTGCT[A/G]AAAAGGAATCTCATT | 317 |
rs533960900 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98663492 | GCACTGGGACTACAG[C/G]CATGAGTCACCATGT | 317 |
rs533961600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707595 | TTTGAGGCCAGGAAC[C/G]CTGGCTGGTCCCCAC | 317 |
rs534035777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714321 | AATACATAATGAACC[A/G]TGTGAAATTACCAGC | 317 |
rs534098411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98706430 | TTTTCAATATTTTTG[C/T]TCTCTTCAAAATGCT | 317 |
rs534113663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729586 | CCAGGGACTGGGGAC[C/T]CCTCTATATTGGGCT | 317 |
rs534120090 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680798 | GTGGGGAAAAGCAAT[A/G]ACAAATTAGTGAGTT | 317 |
rs534156368 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662088 | GAGCTCAGTTCTAGT[C/T]TGGTTTTGGTGCTTA | 317 |
rs534186476 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659446 | TCCTGCTGTTCTATA[A/G]GGAGGATAAGAGAGA | 317 |
rs534195036 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692553 | TCATTCCCCCCTCCC[C/T]AACTCTAGTAGTCCC | 317 |
rs534199115 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726085 | CTCCTAATTGAGTCA[C/T]AGTCTGCATGCTAGG | 317 |
rs534206629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98678383 | GCTCTGTGGAGCTGG[C/T]GGTAGCTGGGGACAA | 317 |
rs534209352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656071 | TACAGGCATGAGCCA[C/T]CGCGCCCGGCCTTGC | 317 |
rs534217008 | in-del | -/A | 0.445724 | 0.155538 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665276 | TATATATATATATAT[-/A]TATTTTTTTTTTTTT | 317 |
rs534299844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718433 | AGAGACAAGGTTTCA[C/T]GATGTTGGCCAGGCT | 317 |
rs534306249 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701096 | TCAGAAAACTTTGAA[C/G]CTTATCCCCTAGCCG | 317 |
rs534370654 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98711857 | CTTAATTTACACTGT[C/T]TTGTGAGTGATTTGG | 317 |
rs534440393 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704024 | TTTTATGTTCAGAAT[G/T]TATACCTAGCTGGCC | 317 |
rs534448310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730597 | GTATTTAGTTTGTAT[A/G]TTTAAATGACAATCA | 317 |
rs534557903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670292 | AGAAATCTGATACTT[G/T]AAAAATGGTAAATTT | 317 |
rs534580284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726187 | ATTTTTTTTAGATAT[A/G]TAATTTTGACTTTTA | 317 |
rs534591977 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98681003 | AACCAGGTGGATGAA[A/C]AAACTAATAATTACG | 317 |
rs534655470 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98673941 | GAAGGAGAGAATGGT[A/T]TCTGAGAGAATTAAA | 317 |
rs534681766 | snp | A/G | 6.67267e-05 | 0.00577572 | downstream-variant-500B, synonymous-codon | APAF1, ANKS1B | GRCh38.p7 | 12:98735587 | GAGTGCCTCCTCAGT[A/G]TGTCTCTCTGATGGT | 317 |
rs534681845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708429 | TGCATCTTACTATAG[A/C]TTGTGTTAGTAAATA | 317 |
rs534690518 | in-del | -/ATA | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98649027 | AACTGTACTGCTGAG[-/ATA]ATAATATGTCTACCC | 317 |
rs534723463 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98717032 | ACCATGCCAAGCTAA[-/T]TTTTTTGTATTTTTT | 317 |
rs534742764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659617 | TTAGCCAGGTGTTGG[C/T]GGCTCATGCCTGTAA | 317 |
rs534751877 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645636 | GGTCTTCGTGCGCCC[C/T]GGGGCTGCAGAGATC | 317 |
rs534785882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680162 | AGTAGCTTTGCCAAG[C/G]TTCCTTTCTGTTTTG | 317 |
rs534837000 | in-del | -/AG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710370 | GTCTTATGCCATCTT[-/AG]TTCGTTTGATTTTTC | 317 |
rs534837290 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98678300 | CTTTTTGATGGCAGC[A/G]GCGGGCTGCCTGGAG | 317 |
rs534922998 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644432 | AGGTCTGGGAGGTTG[C/G]ATCACCTCCGGCTGG | 317 |
rs534986006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682649 | CATAGAACACTTGTC[A/G]TGTTCATTATCTCAT | 317 |
rs535069280 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654816 | TTAAAGTAGTATTTT[-/C]TTTTTTTTTTTTTTT | 317 |
rs535074929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728750 | AAAAAAACCAAAAAT[A/C]AAGTTACATAATTAG | 317 |
rs535169386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98676628 | TTTGGTATGTCTGAA[C/T]AATTGTAGTTTGAGA | 317 |
rs535169837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732325 | TGCTTGAGTTCGGTT[C/G]GGGGGAGGAGATAGG | 317 |
rs535222050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723837 | TTCAAATAATATATG[C/T]AAAAGGACATAACAG | 317 |
rs535279901 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644762 | GGGGGAGCAGGACGT[A/G]GCCGCCTTGGCGTTC | 317 |
rs535343190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690459 | TTGTCAGCCTATTAT[C/T]TCCTGGTTTTTACTC | 317 |
rs535367118 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651008 | GGGATTAAAATTGAC[G/T]AACAATCTATGGAAT | 317 |
rs535415429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98686281 | ATTTAGTCATTTGTC[C/G]CATGGAATGTGCCAT | 317 |
rs535516015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702341 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACCGT | 317 |
rs535550712 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98695403 | ACTCTGTCACACAGG[C/G]TGGAGTGCTGGAGTG | 317 |
rs535561286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687974 | CTGCCACCAAGCCTG[G/T]CTAATTTTTGTATTT | 317 |
rs535658166 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98647204 | GTGGATCACCTGAGG[G/T]CAGGAATTCAAGACC | 317 |
rs535660568 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695389 | TGAGACAGGGTCTCA[C/G]TCTGTCACACAGGCT | 317 |
rs535675653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700405 | ATATAAAATATGGTT[A/G]TATAAGAACTCACTG | 317 |
rs535777018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98664924 | GGCATAATATTGATA[C/T]ATCTTAATTTATTCA | 317 |
rs535820960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98649156 | AATATATGTTCTTGA[A/G]AGGTATTCCATAAAT | 317 |
rs535952410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98691270 | CTTCTTTTCCTGGCA[C/T]CTTGTTTCATTAGTT | 317 |
rs535955298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696011 | ATTTTGTTGCTGCTG[C/T]CTCTTTCTCCATTTT | 317 |
rs536014845 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98672316 | ATTATAGGCGCCCAC[C/G]ACCATGCCTGTCTAG | 317 |
rs536052629 | snp | A/C/G/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98708160 | CCATGTTGGTCAGAC[A/C/G/T]TCTTGAACTCCTGAC | 317 |
rs536096903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716887 | TTATTTTTTTTTGAG[A/G]TGGAGTCTCACTCTG | 317 |
rs536105132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708793 | GACTTGAGATTAAGC[A/G]TAATTATTTTGTATC | 317 |
rs536109059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98717290 | TAGATAGAATATTTT[A/G]TCTCTCTGAGGAGAT | 317 |
rs536168997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668242 | AATTATTTTTGTTTT[C/T]ACCTGTAGTGATTAG | 317 |
rs536177549 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667405 | ACAGGCGTGAGCCAC[C/G]GAGCCCGGCCTCTCT | 317 |
rs536178170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704793 | TTTTGTGTTACTTTG[C/T]TTTTGAGACAGAGTC | 317 |
rs536181010 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689657 | GTAGAGATGGGGCCT[C/T]CCTGTGTTACCCAGG | 317 |
rs536249067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653357 | CATAAATTAAAGAAT[A/G]TTAAGTTGTTAACTT | 317 |
rs536279872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705449 | TTGGACTCTTAGAGA[C/T]AAGGCGGAGAAAATT | 317 |
rs536299490 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98715269 | ATATATATATATATA[C/T]ATATATATATATGAC | 317 |
rs536381161 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659066 | AGATGTGATGGGATT[C/G]TAAATTGGAGTAAAT | 317 |
rs536400596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675546 | TGTTTGTATTGAACA[C/T]GTACAGACTCTTTTC | 317 |
rs536400906 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98668578 | GCATGGAAGGGGAAA[-/T]GAAAGTGATGATAGA | 317 |
rs536419064 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677834 | GAGGAAATAATTGTT[A/G]GAAGACGTAGGGCTT | 317 |
rs536419851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692335 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 317 |
rs536490872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719882 | TTGTGGTGGCAATAT[C/T]TAATTGTATTGTTAA | 317 |
rs536582215 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650193 | TCCCAACTTCTAGTA[A/G]TTAATAATTTTTTTT | 317 |
rs536618843 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656329 | AGAACACAGCTTTAA[A/G]TTTAAGTGAAGTCTC | 317 |
rs536622319 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668212 | TATTAGTAAAAATGG[A/G]ATTATAGCTTGCATA | 317 |
rs536625845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98725637 | GGCCAGGGAAGCATA[A/G]TCCTGAAGTTGTGGT | 317 |
rs536665953 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98670110 | CCACCACACCCGGCT[A/G]ATTTTTGTATGTTTT | 317 |
rs536760464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710708 | GGATTACAGGCAAGA[A/G]CTGCCATGCCCCACT | 317 |
rs536813573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695329 | GTTCTGGGATTACAG[A/G]TGTGAGCCACTGCGC | 317 |
rs536911775 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733295 | GTGCGCACATGCCAG[C/G]CTAATTTTTGTATTT | 317 |
rs536919326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729527 | TCACCTTCTGCTCTG[C/T]GGATGGGTTCCTAAA | 317 |
rs536924890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687863 | GTCGCCCAGGCTGGA[A/G]TACAATGGTGTGATC | 317 |
rs536987934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680049 | CAACACCCCAAAGAT[A/C]CTGTAACATTTTCAT | 317 |
rs536991775 | snp | A/G/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648712 | ATTCTACAATGCTCT[A/G/T]CTACATGAAGGATAT | 317 |
rs536993752 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713364 | TTTTCTCCTCTTCTT[A/G]GAAGCCCAGCCATGT | 317 |
rs537002947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98680951 | CAACCCCAATTTTTT[A/T]AATTTGCTTATGAAC | 317 |
rs537044426 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644376 | AAACAAGGCTGGGCT[C/G]TTTCCTTCCTTTGGG | 317 |
rs537050382 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734760 | AAACCTTAATTTTAT[C/G]AAAAGAAATTTCTGT | 317 |
rs537058143 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670499 | AATAAGGATTGAAGC[A/C]CTGATCTATCATATG | 317 |
rs537122015 | in-del | -/TGAGCTACCACACC | 0.0107246 | 0.0724382 | intron-variant | APAF1 | GRCh38.p7 | 12:98647950 | CTGGGATTATAGGCT[-/TGAGCTACCACACC]TGATTGGAAACTCAT | 317 |
rs537191444 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671216 | CTCCTTTGATTTTTG[G/T]TTATTCTAATTAATT | 317 |
rs537196416 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705151 | TTTTTAGAAACAGTA[C/G]TAAGTAGCAACCCCT | 317 |
rs537207178 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98716267 | ACAGGAAGATGTTGC[-/T]TTTTTTCCGCCTTCC | 317 |
rs537214297 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98687220 | ATACAAAAATTAGCT[C/G]GGTGTGGTGGTGAGT | 317 |
rs537283825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98703195 | TTTTAAGATGAGCAG[C/T]ATTTTTAAAGTATAT | 317 |
rs537415104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689689 | TGGTCTTGAACTAAG[A/C]TCAAGCGATCCTCCC | 317 |
rs537581251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98686166 | TCAGAATCCAAACAA[A/G]CTTTATGTAGCATTT | 317 |
rs537591924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682483 | GTTTACAGAAGAGGA[C/T]GCAGATTCAGAGATG | 317 |
rs537612869 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658467 | ATTAATTTTTCACAG[C/T]AACTCTGAAATAGGT | 317 |
rs537644742 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662460 | TTTTAAATTAGGTCT[C/G]TCTTGATCTTGGATG | 317 |
rs537655394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659443 | TTTTCCTGCTGTTCT[A/G]TAGGGAGGATAAGAG | 317 |
rs537707937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646196 | AACCAGAGTGTCTTA[C/T]TTGCTTAGCTATTGG | 317 |
rs537715225 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98651664 | ATTATTTATTTATTT[A/T]TGTTTTTTTTTAAAG | 317 |
rs537740001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98696441 | TGTTTATGAGGGATC[C/G]ACCCCCATGACCCAG | 317 |
rs537811184 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98693000 | GAACAAATTTACATT[C/T]CCACCAGCAGTGTAT | 317 |
rs537832528 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695765 | GGACTTTTAAAGATT[C/T]CTCTTGACTTAGCTT | 317 |
rs537898921 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717412 | CGGAGTTTCACTCTT[A/G]TTGCCTAGGCTGGAG | 317 |
rs537952599 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718857 | GAGGATCGCTTGAGC[A/C]TAGGAGGTCCAGGCT | 317 |
rs538046271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654416 | TGATTTTTACAAATT[G/T]TATTTTATTTTATTT | 317 |
rs538070611 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720567 | TTGTGAACATTGAGG[A/T]CTACTTTGGTAGTTT | 317 |
rs538126693 | snp | C/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98699785 | ACCGTTTGGGAAATA[C/T]GTTTTGTATTGCTTT | 317 |
rs538127097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98707447 | GTCTCTCTTAATGCC[A/G]TCTAATTCTATGTCA | 317 |
rs538228937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656547 | TTATATTTTAGACTT[C/T]CATGCAGTCACTATT | 317 |
rs538243480 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98659748 | TAAGAGTGAAACTCC[A/C]TCAGAAAAAAAAAAA | 317 |
rs538301875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649060 | TAATTTTTAGAGACA[A/G]TAAGACAATTTATAG | 317 |
rs538336896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704749 | GGCAGTGTTTTGTTG[A/G]GCAGAGACTTTGAAT | 317 |
rs538349020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698263 | TCACTGTGTTGCCCA[A/G]GCTGGTCTTGAACTC | 317 |
rs538378850 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719862 | TTATTTAGTATATAT[A/G]TTAATTGTGGTGGCA | 317 |
rs538400427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681994 | TTTTGTTTGTTGTTA[A/T]ATGGCATAGACTGCT | 317 |
rs538406450 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685042 | TGAGTTTATCTAGGA[C/T]TGGGATAAAGGAGTC | 317 |
rs538418291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731416 | GCCTTAGTGACTGAA[A/G]ACAAATGAATCTCAG | 317 |
rs538457375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694074 | ATAACTGGCTAGCCA[C/T]ATGCAGAAGAATGAA | 317 |
rs538479133 | snp | A/G | 4.94295e-05 | 0.00497115 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723720 | TGTGACATTTCTCAC[A/G]ATGCTACCAAGTTTT | 317 |
rs538501577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724515 | ACTTTCCAACTTCAT[A/C]TTTTTGTGCATGCTG | 317 |
rs538516011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719020 | CTCTTTCCTTTGATG[C/T]CCTTATCCTCGTTCT | 317 |
rs538601899 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650019 | AAGAAATGTTGGCAG[A/G]TATACCACTGACCTT | 317 |
rs538629265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660552 | GTTTCACAGTTTTCA[A/T]TAGCCAAAAGGGAGA | 317 |
rs538639070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98677287 | TGCTGTCATTTGCAT[A/G]TTAGTAATCTGATTT | 317 |
rs538694686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729458 | GAGAAACTAATGCCA[C/T]CACTGATCTCTCAGG | 317 |
rs538707683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721055 | TACAAGTATATATAC[A/G]TTGCAAAAATAGTCA | 317 |
rs538743739 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729386 | TTAGATTCTCGTAAG[A/G]AGTGCACAAGCTAGA | 317 |
rs538885695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726993 | TGAAAAATTAGAGCA[C/T]TGCTTATATATTAAA | 317 |
rs538946765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719772 | CCTTTCTCATTCTTT[C/T]GATCTTGCCATTTTA | 317 |
rs538984479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676709 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 317 |
rs539036602 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710649 | CGCTGGTCTTGAACT[C/T]CTGGCCTCAAGTGCT | 317 |
rs539047955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668505 | TTCTGGGAGGAGGCA[G/T]ACATTAAACAAATTT | 317 |
rs539049578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98677308 | AATCTGATTTTAAGA[A/G]TTTTGTATTTTGGGG | 317 |
rs539079962 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724695 | TTATTCATTTGTTAG[A/G]ACATTTACTTCATAC | 317 |
rs539090638 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733247 | TCAAGCAATTCTCCT[G/T]CCTCAGCCTCCCGAG | 317 |
rs539147380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714462 | AACATCCTGGATGTT[C/T]GATGTTGTTATTCTT | 317 |
rs539179699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717485 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 317 |
rs539205819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672917 | ATGCCACCACGCCTG[A/G]CCGATTTTGTATTTT | 317 |
rs539235552 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644774 | CGTGGCCGCCTTGGC[G/T]TTCGTGGGAACCCTG | 317 |
rs539235688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98653271 | CTTTTAAAAGTACAG[A/G]TAATATAAGAGATCT | 317 |
rs539299934 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98691238 | TCCTGTACTTGTACC[G/T]ACTGTTCCTCCCTTT | 317 |
rs539332062 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98694769 | TCTTAGCTATCTGAT[C/G]CTTTGCTATCTGCTC | 317 |
rs539390214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687699 | CTAATCACTTTTGAA[C/G]GTCCCATCTCTCAAT | 317 |
rs539499634 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644189 | CAGGAAGTAACGGTT[A/T]ATAACAACGTGAACG | 317 |
rs539531556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688847 | TGAAACAGGGTCTTA[C/T]TCTGTTGTCTAGGCT | 317 |
rs539546025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664408 | GTCCATTTTGAAAAT[G/T]TGTGAAACTAAAAAA | 317 |
rs539587293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98681021 | ACTAATAATTACGTT[A/G]CTGGTCTAAAAACAT | 317 |
rs539609215 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670838 | AACTATGGATGTGTT[C/G]TTTCTCACTAGCTTT | 317 |
rs539641482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656889 | TTGAGGTTCATGTCT[C/T]TAACCTTTCCTATTG | 317 |
rs539669635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98661129 | GATGGTCTTGATCTC[C/T]TGACCTCGTGATCTG | 317 |
rs539688847 | in-del | -/G | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644005 | ATTTTTGGTAGAGAT[-/G]GGGGTTTCACCATGT | 317 |
rs539740333 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713024 | GGTTTCACCAGTGTT[A/G]CCCAGGCTGGCCTTA | 317 |
rs539781156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650058 | TGGTAGGTTCTCAGG[G/T]TATTCATCAGGAATA | 317 |
rs539809095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682967 | TTTTTAAACATTAAG[A/G]CAAAATATTGCCATA | 317 |
rs539813801 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98691449 | TGTCATTCTGTTTTT[C/G]TCTTTCCCTTCATGA | 317 |
rs539859053 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728442 | TACATAATTAGTGCC[A/G/T]GGTGTGGTGACTCAC | 317 |
rs539864402 | snp | C/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731432 | ACAAATGAATCTCAG[C/G]TTGGTGGAATGTGCT | 317 |
rs539902353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696883 | TTTGGATTTTAAACC[C/G]TGAAAAAGAAAAAAG | 317 |
rs539913464 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733875 | GTTGGACACTATTCC[C/T]GCTCCCTCTTGTTTC | 317 |
rs539918527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683692 | GCCTTTATTTGACTC[A/G]TTTTGGCTTACATGC | 317 |
rs539927856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676133 | ACTCAAAGTGACAGG[A/G]ATGTAACGTATATGA | 317 |
rs540128016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702397 | GCTCCCACTGGAAGC[C/T]TTTTTGTTTCTTTCT | 317 |
rs540133868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710607 | ATTTTTTTTTGTAGA[A/G]ATGGGGGCATCTCAC | 317 |
rs540139845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98690765 | TCTGCTGTTCTTAAG[C/T]CCCTAACCCTTTTAT | 317 |
rs540142147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703169 | ATGAATTTTCCTTTA[C/T]AGAAAATATGTTTTA | 317 |
rs540163326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658759 | TTGGCATCTAGTGGA[C/T]AGAGACCAAAAAGGC | 317 |
rs540226275 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709364 | GGAAGGCATTTCTCA[A/G]CTAGCTGAAGAGAGA | 317 |
rs540244582 | in-del | -/T | 0.00438594 | 0.0466233 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665385 | CTTTCTTATTTCTAA[-/T]TTTTTTTGGGATAAA | 317 |
rs540362469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700490 | TTGCTTATGAGTTTG[C/T]ACCCCTTTAGCAGGA | 317 |
rs540376842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98693296 | AAAAGGTCTTACTAC[A/G]TTGGCCAGGCTGGTC | 317 |
rs540451792 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98672916 | TATGCCACCACGCCT[C/G]GCCGATTTTGTATTT | 317 |
rs540462354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704941 | CCCACCAGCATGCCC[A/G]GCTAATTTTTTTTTG | 317 |
rs540471057 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98713846 | AGAGAAGAGACTATA[C/T]GCTTAGACACAAAGT | 317 |
rs540484953 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98714581 | TGTGTGCTCAACTGT[G/T]ATGCTATCCTGCCCT | 317 |
rs540514304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698534 | AAGTAGAAAAGTTTT[G/T]GTTTTGGCCATGTTT | 317 |
rs540555878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669671 | GACAATTAGATTGTT[A/T]AAGCATATTCATCTG | 317 |
rs540594544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654737 | TAGGTAGTACAAATT[A/T]AAAAAAATGGAAACT | 317 |
rs540618689 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98662257 | AGAAGGCAGTCTCTA[A/C]TTTTTTTTTTCCTTA | 317 |
rs540638821 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656935 | CATTCATTGACGATT[A/G]GAGTTCGTAGATTAT | 317 |
rs540650398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98699927 | GCTTTCTTCATCACT[C/G]CTTTTTTTTCTTCAA | 317 |
rs540673306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650255 | TAATCCCAGCTGAGG[C/T]GTGGATCACCTGAGG | 317 |
rs540735915 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679278 | GCTGTGCAGATGACA[-/G]GAGGACCAGCTGCAG | 317 |
rs540761979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695714 | AGTAGGGACACAGGC[C/T]CCCTGGGTTGCAGAG | 317 |
rs540769238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647274 | AAAAAAAAAAATAAG[A/G]CAAGGTGGGGGAGAA | 317 |
rs540773754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668863 | AGATATATGAGTCTA[G/T]AATTCTGGGGAGAAT | 317 |
rs540806758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721422 | CTGTTCAGCATAGCC[A/C]TTGATCCTCCAGTCC | 317 |
rs540816328 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684515 | CTCCCCCCACCCCCC[C/G]TCTCATTCTCTCTCA | 317 |
rs540843784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672646 | TTATAAAAAGGAAAG[C/G]ATAGCTATTAATACC | 317 |
rs540854151 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666594 | GCCAATTTAGGATCC[C/T]GTATTGCATATGATT | 317 |
rs540885087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98717848 | GGCTGAAAGCTCTGT[A/G]TGTTGACTGAGATCT | 317 |
rs540914487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661397 | CCAGGCATATTTTTT[A/T]AATCTCTCAGTCTCA | 317 |
rs540967564 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656582 | ACATTGCCAAATTCT[G/T]ATCTAAGTCTTCTTC | 317 |
rs540975748 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698361 | CCCAGCCTGATTTTC[A/G]TATTAATAGGGAAAC | 317 |
rs540987840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98658147 | TGATCTAATGCTACT[A/G]TTTACCATATTTTAC | 317 |
rs541040772 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673337 | ATACAAAAATTAGCT[C/G]GATGTGGTGAATTGT | 317 |
rs541042752 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705442 | TCCCAGCTTGGACTC[C/T]TAGAGATAAGGCGGA | 317 |
rs541139987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696566 | CATAGCAGAGCTGTA[C/T]GTGTTCTCTGCATCT | 317 |
rs541212901 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699250 | AATAATGAAACTGGA[G/T]ATCTTAATTTAAAAG | 317 |
rs541279741 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703244 | TGTTTATGACTGTCA[A/G]TAATTATGCCAGTTA | 317 |
rs541304435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673205 | GGATCTTGTGGCTGG[A/G]CATGGTGGCTCATGC | 317 |
rs541318093 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98664696 | CCACCACCACACCTG[A/G]GTAATTTTTAAATTT | 317 |
rs541370620 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98674269 | AGTTCTTGGATTACA[A/G]GCATGAGCCACCACA | 317 |
rs541396971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727469 | GGAGGATCGCTGGAG[G/T]CTGTGAGGTCAAGGC | 317 |
rs541422123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718755 | GCCTGGGCAACATAG[C/T]GAGACCCCATCTCTG | 317 |
rs541430146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678485 | GTGGACCTGGGAACC[C/T]GCTCCATGGAGCAGG | 317 |
rs541445263 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717985 | GGAGGATAAACCTGG[C/T]TGGCAGGTTCTCAGA | 317 |
rs541452461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731004 | TATGGAATACATGGT[A/G]ATAAATGGTGGTGTG | 317 |
rs541499112 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98667049 | TGTTTAAAGTGGTAT[A/C]TGCCAGGTTTCTGCA | 317 |
rs541542586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670462 | TTATTAGAATTTTCT[A/G]TAAAAAATAATTTTC | 317 |
rs541557346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712963 | ACTGGGACTTCAGGT[A/G]TGCACCACCACACCT | 317 |
rs541561943 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647403 | TTTGAGACAGAGTCT[C/T]AGTCTGTCGCCCAGG | 317 |
rs541570656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662930 | TTTCTGGGAGATTTA[A/G]TATTTTAGGTTCTCT | 317 |
rs541603444 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733378 | CCTCATGATCTACCC[A/G]CCTTGGCCTCCCAAA | 317 |
rs541609894 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660737 | AAATAAAGCATTCCT[C/T]GGGAATGTTATAGTA | 317 |
rs541640946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646354 | CGAATCAATAACTTT[A/T]TATCAGTTTTGTGCC | 317 |
rs541679942 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715197 | TGAGTGTTTTATTTT[A/C]GGGTCCAATATGTTT | 317 |
rs541697886 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643584 | TATTTCTAATATTCA[-/T]TTTTTCCTAATGACA | 317 |
rs541741873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681223 | TGCACCACCATGCCC[A/G]GCTAATTTTTGTAGT | 317 |
rs541754097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682061 | TTTTTTGTTTTTTTT[G/T]TTTTTTTTTTGAGAC | 317 |
rs541829471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722560 | TCTGTGTCTCAGATA[C/T]GTTTGTATGCATATT | 317 |
rs541851994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723092 | TACTGAAATGCCATG[C/T]GAGTAAAAGACTTTA | 317 |
rs541853053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98694943 | GCTGTGGCACCATCT[C/T]GGCTCACTGCAAGAT | 317 |
rs541916254 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98687280 | AGGCAGAGAATTGCT[G/T]GAACCCGGGAGGTGG | 317 |
rs541930021 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732878 | GGTTGACATAATTAA[C/T]GAGAAGAATTTGGAA | 317 |
rs541977928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663646 | GCTTGGAAATACCTT[A/C]TTTTTCTTCTTTTTC | 317 |
rs542039178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656602 | AAGTCTTCTTCTGTC[A/T]TTCCTATGTGTTTCT | 317 |
rs542078854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692609 | GTCTTTGTGTACCCA[A/G]TGTTTAGCTCTGGCT | 317 |
rs542103811 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98708245 | CCCCTGCGCCTGGCC[A/C]AAACTTCTTACCTTG | 317 |
rs542119424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98677848 | TAGAAGACGTAGGGC[G/T]TCATAGCACAGGGAA | 317 |
rs542156788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685496 | GCCGTGCCACCATGC[C/T]TGGCTAATTTTTTGT | 317 |
rs542213540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731970 | GATTCAGTAGAGAGA[A/G]CATTGTTTCCTGTAG | 317 |
rs542250561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98698416 | TGTAACTGAAGGTTC[A/G]GGCTTTTATGTTTAT | 317 |
rs542250810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689945 | GTTGAATATAGGTTT[A/T]TGATCTGCAGGGAAC | 317 |
rs542303175 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726048 | GAGGTTCACATTTCC[A/G]TCATTGTGGGGCAGC | 317 |
rs542357812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682236 | TTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC | 317 |
rs542367409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666862 | TGGTTTTTAAAAAAT[G/T]TTTTGTAGAGATAGT | 317 |
rs542408867 | in-del | -/G | 0.445724 | 0.155538 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665294 | TTTTTTTTTTTTTTT[-/G]TAATGACATCTTAGC | 317 |
rs542412683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98647466 | CAACCTCTGCCGCCC[C/T]GGTTCAAGCAGTTCT | 317 |
rs542420860 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663403 | TTAAAATTTATATAT[A/G]GAATCTCGCTGTGTT | 317 |
rs542421926 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | APAF1 | GRCh38.p7 | 12:98716069 | ATGCACATTCTTTTA[A/C]AATTCAAATAGTATT | 317 |
rs542428682 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98651935 | TCTTCCCACCTCAGC[A/C]TCCGGAGTAGCTGGG | 317 |
rs542429488 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646970 | GAGAACTAATACTCA[A/G]TAGTAACAATGCTCT | 317 |
rs542435834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98711115 | CACAGTACTTCTGGG[C/G]TGAATTGGGATATGG | 317 |
rs542455334 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98700715 | ACTACTATATATTTC[C/T]AAAACTTTTTCATCA | 317 |
rs542466150 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98674925 | TATGGAAGATTGAAT[A/G]AACTCATGTTTCAGT | 317 |
rs542476410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651308 | TCCATGGACAATCCT[A/G]ATGTATTTAATGTAT | 317 |
rs542503189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703628 | GTATTTTCTTTATAG[C/G]CTAATGACCTCTAAC | 317 |
rs542536618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697499 | CAAGTCAAACTAAGA[C/T]TTCTTCAAACTCGGA | 317 |
rs542626713 | snp | C/G | 8.80902e-05 | 0.00663606 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644534 | TTACCAGGCCAGGCC[C/G]AGGCACGTCCCCAGC | 317 |
rs542663001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98653365 | AAAGAATATTAAGTT[A/G]TTAACTTTTAGCTGG | 317 |
rs542665392 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644846 | GCCCAGCCCCTTCCC[C/T]CTCCCCGGCATCCTC | 317 |
rs542775405 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98699864 | GTCCTCTTACACAAT[G/T]TATGCCATCGAATCC | 317 |
rs542819173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720653 | CCAGTATATAGGACT[A/G]TGTTAGTTCTTGCTG | 317 |
rs542820988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98719100 | CTGGTTAATTTTGAG[A/G]GCTCACAAGGCTCAC | 317 |
rs542825849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659873 | CTAAAATTGCTTTTT[C/T]TCTTTGCATGCTACC | 317 |
rs542848441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712078 | CAGCAGCTGCTTTTT[A/G]AACCTTGTAATGCTT | 317 |
rs542867060 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704212 | TCAAGCAATACTCCC[A/C]CAGCCTTGGCCTCCC | 317 |
rs542878760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98721120 | TTGACTAATGGTGGT[A/G]GAAGTTTAGTGATAT | 317 |
rs542934971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676803 | AGGCACGTGCCACCA[C/T]ACCCAGCTAATTTTT | 317 |
rs542994414 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681523 | CCTTTTTCAAAGGGG[A/T]TAAATCTGGAGTACT | 317 |
rs543054796 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98705839 | GCTTTTGTTCATCCT[A/C]TTATTTTTTGGATTG | 317 |
rs543084040 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696164 | GGGTAATTTATAAAG[A/G]AAAGGGGTTTACTTG | 317 |
rs543198438 | snp | A/G | 5.01853e-05 | 0.005009 | intron-variant | APAF1 | GRCh38.p7 | 12:98649446 | TTCAGTAATTATTCC[A/G]AAGTTCTATTCATTC | 317 |
rs543214134 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732852 | AAATTCTGTCTTGAT[A/G]CATTCAAAATGGTTG | 317 |
rs543215771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98724011 | AAATGCAACCTCTAC[C/T]GCATATTGTAGGCAA | 317 |
rs543276628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724831 | TCACAGCGCTTGGAA[C/T]TTGGTAGTTTTCAGT | 317 |
rs543355265 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651686 | TTTTTAAAGAGACAG[A/T]GTGTCACCCTGTTGC | 317 |
rs543389534 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98661008 | CCTGGGTTCAAGTGA[G/T]TCTCCTGCCTCAGCC | 317 |
rs543398079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664524 | GAGATTATGTATATG[C/T]GGTTTTGGATTTTGC | 317 |
rs543398994 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664418 | AAAATGTGTGAAACT[A/G]AAAAAAAAATAGAAA | 317 |
rs543457426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709969 | CAACCTCCACCTCCT[A/G]GGTTCAAGAGATTCT | 317 |
rs543472335 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700134 | CCACATCTAATAGTA[C/G]CTGGTATTTGTGGTA | 317 |
rs543503048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702213 | TGGGACTACAGGCAC[C/T]TGCCACCGCGCCCGG | 317 |
rs543532908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98658064 | AATTCATTTATCTTT[C/G]AGTCTGTTTTTTGCT | 317 |
rs543566508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702444 | TCTTAAATCAGTATA[G/T]TGTATCAATACATGT | 317 |
rs543664267 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721562 | GGAAGCCAGAAATGC[C/T]TCCATTTCTTCCCCT | 317 |
rs543769984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680552 | CACTATCTGAAAATT[C/T]TTTACTTTTTTTTAA | 317 |
rs543772379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98681136 | GTACAATCTCGGCTC[A/G]CTGCAATCTCTGCCT | 317 |
rs543782992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663905 | CTCAGGTGATTGCCC[A/G]CCTCAGCCTCCCAAA | 317 |
rs543790149 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733509 | ATAATCATACCTCAT[C/T]GCAGCCTCAGACTCC | 317 |
rs543831351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98725916 | ATAAATGAATTGCAA[A/G]TTCTGCTTTTTCTGT | 317 |
rs543843520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726377 | TGGGTATTGGGATGA[C/G]TACTTTGGTAACCAG | 317 |
rs543940824 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672757 | ATTTTTATTTTATTT[C/T]ATTTTATTTTTTTTG | 317 |
rs543988888 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98645045 | AGGGGTCGCGCGCGC[C/T]ACGTCGGGCGCGCCG | 317 |
rs544002812 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725874 | CAGAATTTGAGGAAA[A/T]TAATTTTGTAAATTA | 317 |
rs544065483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98653525 | TGCTGGGCGTGGTGG[C/T]GCATGCCTGTAATCC | 317 |
rs544103551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690846 | ACCAAGAGTCCCCTA[A/T]CATAAGCCCCCTCAG | 317 |
rs544106172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689002 | TACTTTTATTAGAGA[C/T]GGGGTTTTGCCTATG | 317 |
rs544169539 | snp | A/G | 0.000119369 | 0.00772466 | intron-variant | APAF1 | GRCh38.p7 | 12:98662809 | AAAGAATGTAAAGGT[A/G]TGGTTATTTATTTGT | 317 |
rs544179627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692461 | GTTTGTTATGTGAGT[A/G]TATTGCATGATGCTG | 317 |
rs544225180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701237 | TCATACTTGGGTTGT[A/G]TATCACATTTTTTTC | 317 |
rs544247166 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729533 | TCTGCTCTGCGGATG[A/G]GTTCCTAAAAGGCCA | 317 |
rs544286655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98722138 | ACGTTTCCCTGCTCC[C/T]ATACTTTAACTCCAA | 317 |
rs544496420 | snp | A/G/T | 1.74598e-05 | 0.00295459 | intron-variant | APAF1 | GRCh38.p7 | 12:98662838 | GTTTATGAGGAGATT[A/G/T]TAGGGAGTTATATAA | 317 |
rs544516909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715334 | ATGGAAATTCTGTAC[C/T]CTCCAGTCTAATTTT | 317 |
rs544528519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700649 | TGCCATTTTAACCAT[C/G]TAAAAATGTGCATTT | 317 |
rs544535123 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656828 | TTGTTCTTGCTCTCT[C/G]TTGTCTCATCCAGAC | 317 |
rs544606958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656077 | CATGAGCCACCGCGC[C/G]CGGCCTTGCCTGGCT | 317 |
rs544609609 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681639 | CCAGACTAAATTTGA[A/G]ACCTTGGAAAAATCT | 317 |
rs544706972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696585 | TTCTCTGCATCTTTA[A/G]CACCTGAACCCTATT | 317 |
rs544755933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674094 | TTGACCTCTTGGGCT[C/T]AAGCAACCCTCCTGC | 317 |
rs544766657 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671033 | ACAGAACTTGTAGGC[C/T]CTGCTCATCTGATTC | 317 |
rs544795967 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98722943 | TATAATTAACTGTTC[C/T]CCAAGCAACTGAAGA | 317 |
rs544828742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665390 | TTATTTCTAATTTTT[G/T]TTGGGATAAATATCT | 317 |
rs544851881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98710314 | TGGGTTTTAGAAGTG[C/T]TTTATTAACTTCTAG | 317 |
rs544889544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658334 | AATAATAATCATGGC[C/T]ATTCCTAGTGTTTAC | 317 |
rs544893755 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702345 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 317 |
rs544955362 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720042 | AGCTGTAAAACTCAG[C/T]GTAATAGTCACCTTT | 317 |
rs544984046 | snp | A/C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655869 | GCTCACTGCAAGCTC[A/C/G]GCCTCCCGGGTTCAC | 317 |
rs545009279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651193 | TTATTCATATTCCTT[A/C]GTTCACGGCTTATTA | 317 |
rs545022429 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98651960 | GCTGGGACCACAGGT[C/G]CATGCTGACACACCC | 317 |
rs545029416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98660071 | CAGGAAGGGGCCAGG[A/G]ACAGTGGCTCATGCC | 317 |
rs545046057 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643759 | TCAAAATATGAGCAC[C/T]CCTCCAAGCTCTGCT | 317 |
rs545077926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697444 | CTAGCATAGTGTTTA[A/G]TAAATGTGTTAAAGA | 317 |
rs545085786 | snp | A/G | 0.00012529 | 0.00791386 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644497 | GCCCACAGGAGGCCG[A/G]CCCAGGCAGCCTCGC | 317 |
rs545126070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652961 | TTATTTTAATTTGCC[A/G]TCTGATTAATTTTTT | 317 |
rs545126539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681325 | CCTTTGACTCCCAAA[G/T]TGCTGAGATTATAGG | 317 |
rs545133464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713628 | TGTTGTCTTTATCAC[A/T]AGTGAAATTCATCCC | 317 |
rs545140449 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653008 | TAGACGAGAACTCTG[A/T]TGTAGTCAAACTAAT | 317 |
rs545146483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98679196 | GGCTTAGCCAGTGCT[A/G]AGCAGACACTGGGAC | 317 |
rs545187407 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735018 | CTTGGGAGGCTAAGA[C/G]AGGAGGATTCCTTGA | 317 |
rs545198603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661216 | CCTCCTTCTCTTGAT[A/C]TTGATCTGTGTAGAG | 317 |
rs545200054 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672258 | CAACCTCTGCCTCCC[A/G]GATTCAAACGATTCT | 317 |
rs545250865 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676199 | AAGTATACATTACAT[G/T]CCTTTACACCTTATT | 317 |
rs545269285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728275 | TTTTGAAATTTCTTC[A/C]GTAATAATAATAGCA | 317 |
rs545328158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708846 | AGTTAAATAAATATA[C/T]ATAAGTCTTGAGCTG | 317 |
rs545372758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720422 | TTTGTAAATGATTAA[A/G]TGGAGGTTTGTTTTA | 317 |
rs545399113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660930 | GGAAAAGCCTACTAG[A/G]TGATTCTGATGCATA | 317 |
rs545407873 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661330 | TTAAAATTGACTTCT[A/G]TTGAGTAAAATAATG | 317 |
rs545467749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723913 | TGCCCATTGGCATTT[A/C]GTTGGTATCAAATGA | 317 |
rs545479433 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98718067 | TTTAGTATGTACACC[-/T]TCCCTTGATCCCTCA | 317 |
rs545495852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663818 | CATGTTCCACCATGC[A/C]TAGCTAATTTTTGTA | 317 |
rs545532020 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98698645 | TGTGCTTTGGAAGCT[G/T]ACTTAAAGCCTGAGC | 317 |
rs545573251 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706699 | ATGGGTAGCACTGAG[A/G]TAAGCAGAATAGGAA | 317 |
rs545581054 | snp | A/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98682183 | CTCAGCCTCCCGAGT[A/T]GCTGGGACTACAGGC | 317 |
rs545604986 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731090 | AGATAGGCTGCCTGA[A/G]TTCAAAGCCTGCCTC | 317 |
rs545673668 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718273 | AGTCTTGCTCTATTG[C/T]CTAGGCCGGAGTGCA | 317 |
rs545754266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679829 | TGCAGCAGTCAGCAC[A/G]TCTGTGCGCAGTGGC | 317 |
rs545754501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675774 | TCCCTCATCAATACT[G/T]AGGAACAACTGTACT | 317 |
rs545873173 | snp | G/T | 1.75928e-05 | 0.00296582 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680341 | AGGATGAAGTGCTTT[G/T]TTGTGCATTCTCTAC | 317 |
rs545903035 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726173 | TTAGAAAACAATCTA[G/T]TTTTTTTAGATATAT | 317 |
rs545928038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98701447 | CCACAGCAGCTGCAC[C/T]GTTTTACATTCCACT | 317 |
rs545932379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673445 | TGTCTCAAAAAACAA[A/C]AAAAAAAAAAACAAA | 317 |
rs545989022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685750 | AAGCAATTCTTATGC[C/T]TCAGCCTCCCAAGTA | 317 |
rs546014793 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693793 | CACTTGTTTTTCAGT[-/T]TTTTTTTTTTTTTTT | 317 |
rs546050898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723135 | TACACTCTCTCCACC[C/T]CTCCAATGAGATAGG | 317 |
rs546064435 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | APAF1 | GRCh38.p7 | 12:98727962 | AGAAAATAAATAAAT[A/T]AATAAATTAATTAAT | 317 |
rs546146867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688139 | GGAAAAAAGCTTATT[C/T]AGCCTTCTGAAATTT | 317 |
rs546159610 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679180 | GCCCATAAAAGCCTC[A/C/G]GGCTTAGCCAGTGCT | 317 |
rs546189882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725044 | CATTTTACAGATGCC[A/G]TGTCTGAAGCTATAG | 317 |
rs546217051 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732996 | TTACCCCAAGGGGGT[G/T]TTGTTCTCCTAAATA | 317 |
rs546229225 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733435 | CGTGCCTGGCCAGGC[C/T]CCTTCTCTTTTAATG | 317 |
rs546352259 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98720716 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 317 |
rs546384354 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690310 | GGTGCTGGGAGCATT[C/T]TTAGGTAGAATATTC | 317 |
rs546397713 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705660 | ATTTACAGCAGAACC[C/G]AGGATAAAATACCAG | 317 |
rs546447781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702104 | GGAGTCTCGCTCTTT[C/T]GCCCAGGCTGGAGTG | 317 |
rs546449665 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714618 | AGGGTTTGTGAGATC[C/G]TTCATCCCGCTCATT | 317 |
rs546480450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690048 | ATTTTCTTGACTACA[A/C]CTTTTCTAGGAAAAT | 317 |
rs546482373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681934 | GGACATTAGTACCTC[A/T]AAAAAGTCAAAATCC | 317 |
rs546494552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682300 | CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 317 |
rs546575677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98727889 | AAGGTTGCAGTGAGC[C/T]GAGATCACACCATTG | 317 |
rs546579266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674639 | GAGGTTAAAATAACA[C/T]ACCCTGGCTCTAGAC | 317 |
rs546607303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98677241 | CTCTTACAAATGCTA[C/T]TTTTGTTATTTTTTT | 317 |
rs546653356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98667336 | GCCCAGGCTAGTCTC[A/G]AAGTCCTGGCCTCAA | 317 |
rs546669018 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679051 | GGGCCTGAAGACTGG[A/G]GGCTGGGCTGCTGGT | 317 |
rs546755962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660482 | TTTGTTCAACAGTTA[A/G]TTAATTCAGCAAATA | 317 |
rs546775994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713172 | CTATTAGTCATTGTT[C/T]GTTAAACTAACAATC | 317 |
rs546952447 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735367 | TTTTTGCCTTGGTAT[A/G]CATTTTAAAATATGA | 317 |
rs547042610 | snp | C/G | 3.29538e-05 | 0.00405904 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683182 | CTAGTACACACCTAT[C/G]ATGAGCACTCAGAGC | 317 |
rs547046735 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659996 | TCTTACTTTGAATCC[A/G]TTATTTCTAATGGGT | 317 |
rs547109573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684093 | TTGCAATTGAACATG[A/G]TATTTTTGAGAGGGG | 317 |
rs547171587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716376 | GAAATTTTGTTTAGA[G/T]CCTTCCTGTTACTAT | 317 |
rs547213421 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733228 | CAATCGCTGCCTCCT[A/G]GGTTCAAGCAATTCT | 317 |
rs547238337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98664964 | GTATTATTGGACATT[A/G]TTTACGTTGTTTAAG | 317 |
rs547285886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98691131 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAAGTTG | 317 |
rs547318975 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645163 | CGCGCGCGGGCATGA[A/G]CCGTGGCAGGAGTGC | 317 |
rs547436839 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727440 | AAAAGGCTGCTACTC[C/T]GGAGGCTAAGGTGGG | 317 |
rs547474441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98650720 | CTAACCCTTGGTTTT[C/T]CCCCTCTATCATTAC | 317 |
rs547515484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703126 | AAGCTTTTATTTCTC[C/T]TTAGGCTAGCTTGAG | 317 |
rs547527888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98696142 | CTGAAACATAATACC[C/T]GAGACTGGGTAATTT | 317 |
rs547587792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656414 | CTCAGGAAACTTTAG[A/G]AGTAAGCAGTAGGGC | 317 |
rs547661094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664925 | GCATAATATTGATAT[A/G]TCTTAATTTATTCAA | 317 |
rs547672538 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725535 | GATGACAATGGAGAA[A/T]TCAGGGTAGGCTGTT | 317 |
rs547688311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702231 | CCACCGCGCCCGGCT[A/G]ATTTTTTGTATTTTT | 317 |
rs547699528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656867 | CTCCCTTCTCCAGCT[G/T]AATGCTTTGAGGTTC | 317 |
rs547756732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98661570 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 317 |
rs547825431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703830 | GTATAGATATGTGGC[A/G]TTTCTTAAACAGTGT | 317 |
rs547886343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696776 | GCTAGGATTACAGAC[A/G]TGAGCCACTGCACCC | 317 |
rs547903588 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727548 | CGACATCCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 317 |
rs547950850 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650614 | AAATATGGAGGCTAG[A/G]GTATATCTATGTGTA | 317 |
rs547976663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725985 | ATAGCCATTTCCAGT[C/G]TGGTTTGTTGCAGTC | 317 |
rs548013879 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653024 | TGTAGTCAAACTAAT[C/T]AGTTTTTTTTTTTGT | 317 |
rs548015798 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709930 | GCCTAGGCTGGAGTG[C/T]AGTGGCACGATCTTG | 317 |
rs548026818 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | APAF1 | GRCh38.p7 | 12:98655437 | CTCACCTCCCGGACG[A/G]GGCGGCCGGCCGGGC | 317 |
rs548044420 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98680758 | CAAAAATGCCTAGGT[A/T]GATCACCTCAGGATT | 317 |
rs548079128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668325 | TTACTAGTAGCTTTC[C/T]TTTTTGGGCAGTATG | 317 |
rs548079850 | snp | A/G | 0.000181559 | 0.00952609 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665650 | GAATAAGCAGTTTAA[A/G]AGAATAAGGAAATCT | 317 |
rs548092364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98729249 | ATCAGCGGTCCCCAG[C/G]CTTTTTGGCACTAGG | 317 |
rs548186398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723565 | TATAGACCTGTCTTG[C/T]AGCTGATTATGCTTT | 317 |
rs548186871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98677184 | TTCCAACTCAGTGAC[A/G]TTTGTAACACGTGAC | 317 |
rs548189117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714293 | TCCCTCAAAGTCATC[A/G]AATAATATAAATAAT | 317 |
rs548212272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98706364 | TGTAGTTTTGATAGT[A/G]TGTTTCTGAGCAATA | 317 |
rs548252852 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98654096 | AAGCTAAATTGCTCC[C/G]TCTTGTGCCCATAGT | 317 |
rs548262541 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98720810 | TCTACTAAAAAATAC[-/A]AAAAAAATTAGCCAG | 317 |
rs548284987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731271 | TTATGAACATCCCCC[C/G]ACCAGAGATGTGCAT | 317 |
rs548294189 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645695 | TGCCCCGGGGCGAAG[A/G]GTATGTGGCGAGACA | 317 |
rs548328611 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98678649 | CTCAGGCATCCCTGT[A/T]CTCTTGGGGGACCTG | 317 |
rs548362480 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98679396 | AAGGAGCTGCCCCCC[A/G]CAGGTTTATTGAGCT | 317 |
rs548390374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670914 | GAGGTTAATGATGTT[A/T]TACCTAAAATTTTTT | 317 |
rs548411644 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98720923 | AGTGAGCTGAGATCC[C/T]GCCACTACACTCCAG | 317 |
rs548419530 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692857 | AGTGAATATACAAGT[G/T]CATGTGTCTTTTTGG | 317 |
rs548460401 | in-del | -/TTA | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665497 | TAAGTAAGTCGATTC[-/TTA]TTAGTGACAAAATAG | 317 |
rs548492139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98685924 | TTACAGGGGTGAGCC[A/G]CCATGTCCAGCCTGA | 317 |
rs548593082 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692209 | TGCCTCAGCCTCCCT[A/C]GTAGCTGGGAGTACA | 317 |
rs548713142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663338 | TAGAAACTATTAGCT[C/G]TTTGTCATATTTTTA | 317 |
rs548823148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696652 | TTGAAACTTGGGAGT[C/G]ATCTTTTTGTTTGTT | 317 |
rs548866803 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716470 | GACCTTTGGGTGTAG[A/T]TGGAAATTATTTTAC | 317 |
rs548884575 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | APAF1 | GRCh38.p7 | 12:98689465 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTCTGTGTG | 317 |
rs548994856 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704122 | TTCAAAGATGGATTA[A/G]TGCTTTTTTTTTTTG | 317 |
rs549016992 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727840 | CAGCTACTTGGGAGG[C/G]TGAGGCAGGAGAATC | 317 |
rs549041592 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733774 | ACTTGTATGTTGGAA[A/G]GAGTAGATTTTATTG | 317 |
rs549056283 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707211 | AAGCTTCTCCACAGC[A/G]TGGCCTTATTCTGCT | 317 |
rs549065510 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98653137 | GTCTGCCTTTGTATG[A/T]CCACTAATTCAAGAA | 317 |
rs549090091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705221 | TGCCATCCTTAGCAA[C/T]CTCCAGGAAACAATG | 317 |
rs549112519 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645120 | AGGCTTAGCCACGCC[C/G]CGTCCGCGGGGTAGG | 317 |
rs549158737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719585 | TCTCGATCTCTTGAC[C/T]TTGTGATCCTCCCGC | 317 |
rs549283931 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716395 | TCCTGTTACTATGAT[C/T]ACTGTGTACTAAGGG | 317 |
rs549298256 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649315 | TGTTTGTCTTTGCTC[C/T]CTGTTGTCTGAGAAA | 317 |
rs549304525 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98711758 | TAGGTAATCTTTGTT[C/G]AAGCATTGTAAATCC | 317 |
rs549340496 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644018 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTAGT | 317 |
rs549445654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690270 | GGTAGAATTCTACTT[C/T]GTAGAGTTTAGCTAG | 317 |
rs549455782 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98691004 | ATGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC | 317 |
rs549476605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683077 | AAGCAATGGACATTG[C/G]TTTGCCCCTCTGTTC | 317 |
rs549560408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712501 | AATTATATGTCTGGC[A/G]TTGTGCACTTCTATT | 317 |
rs549570204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659517 | AGCACTTTGGGAGGC[C/T]GAGGCTGTTGGATTA | 317 |
rs549680831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660219 | GGTGTGGTGGTACAC[A/G]CCTGTGGTCCCAGCT | 317 |
rs549713023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715651 | ATTTTAAACACATTA[C/T]GTTGGGCATACATTC | 317 |
rs549736101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708481 | AATATTGAAACCTTT[C/G]TAGCATCATAGGTAT | 317 |
rs549736726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664907 | GAAAAAAATTTACCA[C/G]TGGCATAATATTGAT | 317 |
rs549851070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98701537 | TTTAAAATTATAGCC[A/G]TCCTAGTAGGTGTGA | 317 |
rs549863618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694606 | TCCTTTTAAATATTA[C/T]TCTGTTCTTGTTTCA | 317 |
rs549889334 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670105 | GTGCACCACCACACC[C/G]GGCTAATTTTTGTAT | 317 |
rs549930327 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661657 | ATATTATATTAGAGA[C/T]GGGGTTTCTCCATGT | 317 |
rs549938748 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98715236 | GCATACATGGTGTGC[A/G]TATATATATATATAT | 317 |
rs549973717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670798 | TTTGGAGCTGAAGTA[C/T]GAGGCCCATTTTATG | 317 |
rs549978827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702322 | CACCTGCCTTGGCCT[C/T]GCAAAGTGCTGGGAT | 317 |
rs549993049 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723459 | TGTTAATTGCAGTCA[C/G]CTACATCTGCTGTGT | 317 |
rs550011792 | in-del | -/TTTA/TTTATTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672157 | TCCATGAAGATTTTA[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 317 |
rs550055645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672261 | CCTCTGCCTCCCGGA[A/T]TCAAACGATTCTCCT | 317 |
rs550060632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732320 | CTGTTTGCTTGAGTT[C/T]GGTTGGGGGGAGGAG | 317 |
rs550068084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98672825 | AATGGCACGATCTCC[A/G]CTCACGGCAACCTCC | 317 |
rs550139152 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98679465 | CCTTCCACCTGTCAG[C/T]GTACCACATTCTTCC | 317 |
rs550168603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667261 | CCACCACACCTGACT[A/G]ATTTTTTTTATTTTT | 317 |
rs550215511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710374 | TTATGCCATCTTTTC[A/G]TTTGATTTTTCTTGA | 317 |
rs550239651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668979 | GTTTACATTTGGAAA[A/C]CCATATGTACTTTCA | 317 |
rs550259951 | in-del | -/T | 0.0012 | 0.0244655 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665385 | TTTCTTATTTCTAAT[-/T]TTTTTTTGGGATAAA | 317 |
rs550295957 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710208 | TTTTTTGTATTTTTA[A/G]TAGAGATGAAACTAT | 317 |
rs550308325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98721585 | CTTCCCCTTCCCCCA[A/G]CATATCTCATTGGGT | 317 |
rs550369448 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98713962 | GTTTTCTCTTTATTA[C/T]TGTGAAAAATTTATT | 317 |
rs550415811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724525 | TTCATCTTTTTGTGC[A/G]TGCTGCTAACTTTGG | 317 |
rs550443784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679904 | ACTCGCCCTTGGCAG[C/G]CTTGGGACCCAGGCT | 317 |
rs550456527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98675489 | ATATCCATAGATTCA[A/G]CCAACCTGGATTGAA | 317 |
rs550469158 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | APAF1 | GRCh38.p7 | 12:98667483 | TTATAAAATTGTTTC[C/T]GGCTTCTGAAACGTT | 317 |
rs550517908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729505 | GTAATGTTCACTCAC[C/T]AGCCGCTCACCTTCT | 317 |
rs550534062 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98682211 | GGCGGCCGCCACCGC[C/G]CCTGGCTAATTTTTT | 317 |
rs550540151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98720828 | AAAAATTAGCCAGGC[A/G]TGGTGACAGGCACCT | 317 |
rs550554219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713200 | ATCATCTTATCCAGT[G/T]GGCTGTATATTTTTC | 317 |
rs550561608 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709456 | GATGCCCTAAGAGCA[A/G]ATGCCCTAAGGAGCA | 317 |
rs550578877 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689305 | TCAGCTACTGTCCCT[C/G]TATGTGTTTCTTGGG | 317 |
rs550579617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730236 | GAGAAATGACCACCA[A/G]TTGTTCTCCTTTAGT | 317 |
rs550590345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683042 | AAAATCTGCTATGAC[A/G]GGATAAGATAGCATT | 317 |
rs550699837 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716219 | AGTGCTCTTCTTGAT[C/T]TTCCCATTTGAGAAG | 317 |
rs550747059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698975 | TGCTCTGCTAGGTCA[C/T]GACCTAACTTGGACT | 317 |
rs550750358 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735483 | TCTGTTGATTAGACC[A/C]CTAAAGTGAAGGATT | 317 |
rs550754846 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687851 | CAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC | 317 |
rs550807613 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735867 | AGGGGAAGGGGTTAC[A/G]GTTTTAGATGGACTG | 317 |
rs550824779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700054 | GAACAAGATAGTGAA[A/T]TTTTTATAAAGTAAA | 317 |
rs550912589 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733259 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 317 |
rs550921129 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98728602 | GGCGGGCACCTGTAG[C/T]CCCAGCTACTTGGGA | 317 |
rs550927820 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664678 | AGCTGGGACTGCAGA[A/T]ACCCACCACCACACC | 317 |
rs551002131 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660968 | TATTTTTATGGTGCA[A/G]TCTCTGCTCACTGAA | 317 |
rs551014146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692790 | TTCCTTTAACCTTCC[A/G]TTGATGGGCACCTAG | 317 |
rs551103442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670086 | AGTAGCTGGGAGCAC[A/G]GGTGTGCACCACCAC | 317 |
rs551147132 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685548 | CATTATGTTGGCCAG[G/T]ATGGTCTCAATCTCC | 317 |
rs551147904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709425 | TGGTATTCAGGAGCT[C/T]GGAGTGGTGGTAACA | 317 |
rs551199444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98702287 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 317 |
rs551217396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692223 | TAGTAGCTGGGAGTA[C/T]AGGCGCCCGCTGCCA | 317 |
rs551315918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651577 | AACTCTCTGCTGCTG[C/T]AGCAAAGCTGGGTTG | 317 |
rs551337360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695199 | CTGGGATTACAGGCA[C/T]GCACCACCACACCTG | 317 |
rs551354190 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730940 | GTACATACTGAATGA[C/T]AAGAAATTCACATTA | 317 |
rs551369009 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644242 | TCAGAAAGCGTGGCC[A/G]AATCTGCAGCTCTTA | 317 |
rs551384691 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98688665 | TTTTTTTTTTTAGAG[A/G]TAGGATCTTACTATG | 317 |
rs551388057 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668425 | ATTGAGTGCTTGTTA[A/T]GTATATTGCTCTTCA | 317 |
rs551491376 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98680901 | GTTGCTGCACAAACT[C/T]GGGGATTCCTGTTGT | 317 |
rs551574711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98648975 | ATATTTTTTATTTGC[A/G]TCCACATTAACTCTC | 317 |
rs551580001 | snp | C/T | 0.000115396 | 0.00759505 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671038 | ACTTGTAGGCCCTGC[C/T]CATCTGATTCATGAA | 317 |
rs551667681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695875 | CTGGGTGCCAGCACT[G/T]CCTGAGTCTTTTTGG | 317 |
rs551709084 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98655806 | TTTTTTTTTTTGAGA[A/C]AGAGTCTCACTCTGT | 317 |
rs551766092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646951 | GCTGACATCCTCCTT[C/G]AACGAGAACTAATAC | 317 |
rs551768246 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656285 | TTTTCCAAACTTTAT[A/T]CTCTGCAATTATAAA | 317 |
rs551859759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697909 | TGCTTTTCAGGCTCT[A/G]AGATGAACTGTTTTA | 317 |
rs551873978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98690165 | ACTGTTTTGATTCTG[A/G]TACTCTGGTTGAATC | 317 |
rs551902275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647674 | TGCGCCCGGCCCCCA[C/T]GTTATGTGTTGTATG | 317 |
rs551947262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656104 | GGCTAATTTTTTGTA[C/T]TTTTTTAGGGACGTG | 317 |
rs551951062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98718770 | CGAGACCCCATCTCT[A/G]CAAAACAAAATAATT | 317 |
rs551951286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730038 | TATCCCAATTATCCT[A/G]ATTTGATCATTACAC | 317 |
rs551982391 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682770 | CACAAGTCATAAGTG[A/G]TAGAGCCAGCTCTTG | 317 |
rs552008548 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657497 | ACCTTGTGCAGGTTC[A/G]AAGACTCCATGTCAC | 317 |
rs552032520 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666283 | TTCTGTGATCGGAAT[A/G]GAAAGTCGTTTCGTT | 317 |
rs552092526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659396 | ATGTCCCAATAAGAT[A/G]TAACTACTGACCTCT | 317 |
rs552099441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722590 | TTTGTGCTAGTTACT[C/T]ATGTTATTTCATTCC | 317 |
rs552120645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672097 | GTTACAGGTTTTTCT[C/T]TCATATGTAAAATGG | 317 |
rs552178930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707362 | GCTCTACTTACCTGT[A/C]TCTCTGTTTGTTGAA | 317 |
rs552203010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692988 | TACAAAGTCACCGAA[C/G]AAATTTACATTCCCA | 317 |
rs552228477 | snp | A/T | 0.000369543 | 0.013588 | intron-variant | APAF1 | GRCh38.p7 | 12:98662448 | TTAATATTTTTTTTT[A/T]AAATTAGGTCTCTCT | 317 |
rs552311949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669255 | TTCCTTGGCAAATTC[C/T]GAGAAGTAGAATTAC | 317 |
rs552348448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721851 | ATTTTAAGATTTTGC[C/T]TAGGTCTGATTAAAG | 317 |
rs552369500 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98664032 | TTATTTATTTTATTT[A/G]TTTTTTGAGACGAGT | 317 |
rs552379369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718662 | ATGGCCTTACTGGGC[A/G]CAGCGGCTCACACCT | 317 |
rs552379706 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654079 | TACAGCCTCCTCATG[C/T]AAAGCTAAATTGCTC | 317 |
rs552413406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98714341 | AAATTACCAGCATTT[A/G]CCTATAAAGTGGCAG | 317 |
rs552444759 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98678832 | GCTGACATGCCAGCC[C/T]CCTGCCGCCTCGGCC | 317 |
rs552458211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679303 | CTGCAGAGAGGAGCT[A/G]CCCTCTCTGCTGATA | 317 |
rs552560602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98711951 | TTTGAAATGTAGCAG[A/G]AAAGTATATTTTAAC | 317 |
rs552615545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717149 | CTGGGATTACAGGCA[C/T]GAGCCCCCGCACCTG | 317 |
rs552639887 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665539 | AGCATAGTGACTTCA[-/T]TTTTTTTTTAAAGGC | 317 |
rs552692684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718998 | CCCTCTCAGTTATTT[C/T]GACCTTCTCTTTCCT | 317 |
rs552696308 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703443 | ACCATCCAGTACTGT[A/G]ACTTCTCCCCACAAA | 317 |
rs552779382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681017 | ACAAACTAATAATTA[C/T]GTTACTGGTCTAAAA | 317 |
rs552781252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673216 | CTGGGCATGGTGGCT[A/C]ATGCCTGGAATCCCA | 317 |
rs552819668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731373 | TGCTGTACATTTTTC[A/G]GGTAGTTGAACTAAG | 317 |
rs552841078 | snp | A/G | 0.00015963 | 0.00893249 | intron-variant | APAF1 | GRCh38.p7 | 12:98671124 | TTAGTGCTAAAAAGG[A/G]ATCTCATTTTTTTTT | 317 |
rs552931457 | snp | A/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731947 | GCATCACACCTGGGG[A/T]AAGGGAAGATTCAGT | 317 |
rs552931863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732208 | AACGGTTGGAGTTGG[A/G]TGTAGGCGGAGCAGT | 317 |
rs553016698 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650902 | TGAACTTTCTTTGTG[C/T]ATTTATAATATTCCA | 317 |
rs553018950 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653018 | CTCTGATGTAGTCAA[A/G]CTAATCAGTTTTTTT | 317 |
rs553107362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728768 | GTTACATAATTAGTA[A/G]ATAGAAAAGCCAGGA | 317 |
rs553142755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651933 | GATCTTCCCACCTCA[A/G]CCTCCGGAGTAGCTG | 317 |
rs553163136 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733806 | TCTACCCTTTTCTCA[C/G]TGTAGCTGCTGGCAG | 317 |
rs553197097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668477 | ACAAAGTCATTGCTC[C/T]CACGAGTTTATGTTC | 317 |
rs553220636 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98673942 | AAGGAGAGAATGGTA[A/T]CTGAGAGAATTAAAA | 317 |
rs553229264 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734988 | TGCGGTGGCACGTGC[C/G]TGTAATCCCAGCTCC | 317 |
rs553246733 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699289 | AAAGTCATGCATAGG[G/T]AAAAATAATTCATCA | 317 |
rs553290965 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735589 | GTGCCTCCTCAGTGT[G/T]TCTCTCTGATGGTTC | 317 |
rs553301709 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644765 | GGAGCAGGACGTGGC[A/C]GCCTTGGCGTTCGTG | 317 |
rs553330312 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98698258 | AGGTCTCACTGTGTT[G/T]CCCAGGCTGGTCTTG | 317 |
rs553345615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720195 | TTGACGATTTCAGGT[A/G]TTCTCAGCTAGGGGG | 317 |
rs553415282 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695447 | GCAGCTCACTGCAGC[C/T]TCAACCTCCTAGGCT | 317 |
rs553425177 | snp | G/T | 3.295e-05 | 0.00405881 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667549 | ACTCAGTTTCAGAGA[G/T]ATCACCAGCCGCATA | 317 |
rs553434211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675725 | GACTTGAGCATCCAT[A/G]GATTTTGGTATCTGT | 317 |
rs553449336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731545 | CAAAGTCCATTGGGT[A/G]TACTTTTAGCAGTTA | 317 |
rs553456492 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693325 | TCTCAAACTCCTGGC[C/T]TCAAGTGATCCTTTG | 317 |
rs553497662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98676647 | TGTAGTTTGAGAGAA[A/G]CAGTTTTTTTTTTTT | 317 |
rs553504857 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644464 | TGTTGAGCCGGGTGG[A/G]AGCCCAAACAGCAGG | 317 |
rs553530257 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98713030 | ACCAGTGTTGCCCAG[C/G]CTGGCCTTAAACTCT | 317 |
rs553589759 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690889 | AAAGCCTCTGCTCCA[C/T]TTTTTCTCATAACAG | 317 |
rs553636414 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98647247 | ATGGTGAAACCCCGT[C/G]TGTACTAAAAAAAAA | 317 |
rs553664972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700434 | TGAGGGATCATGTAT[A/G]TGATTGTTATTGATT | 317 |
rs553788257 | snp | C/T | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729600 | CTCCTCTATATTGGG[C/T]TGATCACTTGGACAT | 317 |
rs553800380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688001 | ATTTTTAGTAGAGAC[A/G]GAGTTTCACCACGTT | 317 |
rs553821159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679611 | GAAAAGCTGCGGCCC[C/T]TCGGGGAGCCCAGAC | 317 |
rs553861570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680229 | ATTGAATGATGACCA[A/G]TAGTTAAGCAGTTTA | 317 |
rs553865848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688816 | TCTTCTCTTTTCTTT[C/G]TTTCTTTCTTTTTTT | 317 |
rs553910376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664253 | TGAACTCCTGACCTC[A/G]TGATCCACCTGCCTC | 317 |
rs553946303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716111 | TATGAAAAACAGACC[C/T]TTTCCCCCATTTCTC | 317 |
rs554013473 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733331 | AGAGACGGGGTTTCA[A/C]CATGTTGGCCGGGAT | 317 |
rs554064516 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98685679 | CTTCCTCTATCACCC[A/G]GGCTGGAGTGCAGTG | 317 |
rs554114837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98702351 | ATTACAGGCGTGAGC[C/T]ACCGTGCCTGGGCTA | 317 |
rs554125919 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98686344 | GGTACTTGACTTGCT[C/T]CACCATTTTTAGGGT | 317 |
rs554136379 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98702020 | TTGGCCTCCGGCGCT[A/T]CGCTGCCTACCATAT | 317 |
rs554176574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695513 | GGGACTACAGGTGTG[C/T]ACCACCATGCCTGGC | 317 |
rs554204215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649186 | TGTTCTTCCTTTTAC[A/G]CTTGCCTTCCCAGTC | 317 |
rs554215201 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728589 | AGCTGGGTTTTGTGG[C/T]GGGCACCTGTAGTCC | 317 |
rs554247035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705470 | GGAGAAAATTTCATA[C/T]AATTAGTTCATAACC | 317 |
rs554312135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699196 | ATTTTATGTTCTGCA[G/T]TTTGGGCAGTGCTTC | 317 |
rs554357301 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645276 | TCCGGCGGGATTTGA[C/T]TGCTCCGCTGTCCAG | 317 |
rs554409740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708811 | ATTATTTTGTATCTA[A/G]CAGGTGTCCAGCAGA | 317 |
rs554453702 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98661185 | GGATTACAGGCGTGA[A/G]CCACTGCGCTCGGCC | 317 |
rs554457354 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650200 | TCTAGTAGTTAATAA[-/T]TTTTTTTTTTAGTAG | 317 |
rs554475345 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98726777 | TGGTACATTAAAAAA[A/T]TTTTTTTCTCCCTGA | 317 |
rs554477555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709570 | TGATAGCGTTGTAGA[C/T]AGTGGCAGCAAGAGA | 317 |
rs554552223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98715270 | TATATATATATATAT[A/G]TATATATATATGACA | 317 |
rs554653099 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686004 | TTAAGCATGCATCTC[A/G]GAGATCTTAAATATA | 317 |
rs554732772 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | APAF1 | GRCh38.p7 | 12:98707531 | TACTCCTTATTTCCA[A/G]CACTCCACTGCTTCT | 317 |
rs554809886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98652500 | TGGGTTTCTTTTTTT[A/G]TGGATTTTGTTTATA | 317 |
rs554811266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712843 | TTTTTTTTGAATCAG[A/G]ATCTCACCTTGTTGC | 317 |
rs554815984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704821 | GTCTCTCTCTGTCAC[C/T]CAGGCTGCAGTGTAG | 317 |
rs554874293 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98713233 | ATTTCCTTTATTACT[A/G]TTTCTCATGCTTTTT | 317 |
rs554950490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718367 | CCTCCTGAGTAGCTG[A/G]GATTACAGGCACCTG | 317 |
rs554951984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98706675 | AACCTCCTACAAACT[A/G]AGAAATTGATGGGTA | 317 |
rs554955493 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677454 | TCACGAATCTTTCCC[A/G]CTTAGTTGTCCGCCC | 317 |
rs554966001 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98669568 | TGAATGGTCATCTTT[G/T]CATGTCATTTATATA | 317 |
rs554984806 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697391 | AACTCATTGAGGGTA[A/G]TATCTGTATCTGATT | 317 |
rs554992830 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689165 | TAAACTGTAGGAAAC[A/G]CAGACTCATTGGGAT | 317 |
rs555001637 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720898 | CATGAATCTGGGAGG[C/T]GAAGCTTGCAGTGAG | 317 |
rs555030077 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688994 | ATTTTTTGTACTTTT[A/G]TTAGAGATGGGGTTT | 317 |
rs555106753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673832 | ATAATTACAATATAA[C/T]GCAATGAGTATAACA | 317 |
rs555113837 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98656018 | TCGATCTCCTGACCT[A/T]GTGATCCGCCCACCT | 317 |
rs555126865 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98695351 | CCACTGCGCCCAATG[C/T]CGCCCCCCCCCTTTT | 317 |
rs555161676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724911 | AAAAAAAAATAGCAT[C/T]TGGCTGCCAAGAAGT | 317 |
rs555171028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676860 | ATGTTGGCCAGGCTG[A/G]TCTTGAACTCCTGAC | 317 |
rs555255895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687255 | GTAATCCCAGCTACT[A/T]GGGAGGCTGAGGCAG | 317 |
rs555321120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98679717 | CACCACCGTGTTCCC[C/T]GGTGCCAGCGTGTAA | 317 |
rs555377192 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668543 | TTCAGTGGGTAGTTA[A/G]GTGCTCAGAAGAAGG | 317 |
rs555410006 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98710727 | CCATGCCCCACTCAA[A/C]CCTTAACAAGTTGTA | 317 |
rs555444396 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705157 | GAAACAGTACTAAGT[A/G]GCAACCCCTCTTTCA | 317 |
rs555450846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658948 | GCCACAGATTTACTT[C/T]AAACTTCAGTTTCTT | 317 |
rs555463331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98667021 | ATTATGGGTGATGTT[A/G]ATGTTGATAATTTGT | 317 |
rs555479091 | snp | A/G | 1.66197e-05 | 0.00288263 | intron-variant | APAF1 | GRCh38.p7 | 12:98727347 | GAACTGTGAAAGAAA[A/G]TAATAGCCTATATCA | 317 |
rs555492568 | in-del | -/ATTTT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665278 | TATATATATATATAT[-/ATTTT]TTTTTTTTTTTGTAA | 317 |
rs555498615 | snp | A/T | 9.21786e-05 | 0.00678829 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735535 | TCTATTTAGGCTTTA[A/T]CAGCTATATGTAAAT | 317 |
rs555537625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682528 | AGCTTACATTAAACT[G/T]GGAACAGTAATAGGG | 317 |
rs555558578 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733311 | CTAATTTTTGTATTT[C/T]TAGTAGAGACGGGGT | 317 |
rs555603169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675567 | GACTCTTTTCTTGTT[A/G]TTATTTCCTAAACAC | 317 |
rs555607893 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699080 | CAGCAGTGGCAAGTC[A/G]TGAGTCTCTTCATCT | 317 |
rs555689924 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734832 | TTGTACACACTGTTA[C/G]GGGCTCATCTCATGT | 317 |
rs555724168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673054 | TGAGCCACTGCACCC[A/G]GCCTAAATTTTATTT | 317 |
rs555768404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651676 | TTTTTGTTTTTTTTT[A/T]AAGAGACAGAGTGTC | 317 |
rs555777929 | snp | G/T | 0.432797 | 0.170544 | intron-variant | APAF1 | GRCh38.p7 | 12:98682052 | ATGATTAATTTTTTT[G/T]TTTTTTTTTTTTTTT | 317 |
rs555781533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689696 | GAACTAAGCTCAAGC[A/G]ATCCTCCCACTTTGG | 317 |
rs555790344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98674932 | GATTGAATGAACTCA[C/T]GTTTCAGTTAGTGGC | 317 |
rs555794462 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675145 | TATTCAAAGAATGCT[C/T]TATTTAAGTACTAGA | 317 |
rs555815025 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644418 | GGCACAGAAGGCCCA[A/G]GTCTGGGAGGTTGGA | 317 |
rs555848536 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717461 | GCTTGCTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 317 |
rs555930609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719164 | TCAGTGTCTCCTGCT[C/G]TTCTCTAGTTGTTCC | 317 |
rs555998732 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98672737 | AGTTTATAAGGTAAA[-/T]TTTTATTTTTATTTT | 317 |
rs556038973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696496 | CCAACACTGCCACAG[C/T]GGGGATCCAATTTCA | 317 |
rs556051078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689015 | GATGGGGTTTTGCCT[A/G]TGTTTCCCAGGCTGG | 317 |
rs556055705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98654427 | AATTTTATTTTATTT[C/T]ATTTTATTTTGAGAC | 317 |
rs556068837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647120 | TGTGTGCTAAAAAAA[A/T]TTGACAGTAGAGGCC | 317 |
rs556134012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701295 | GTTTGTTTCCACCTT[G/T]TGGCTACTGTGAATA | 317 |
rs556144486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701910 | TGTGGAATAGGCAAG[C/T]TTGCCAAGTTTCCTC | 317 |
rs556146460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694244 | CCAAGTCCTCAAAAG[C/T]AATTGCTACAAAAAC | 317 |
rs556177872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98693005 | AATTTACATTCCCAC[C/G]AGCAGTGTATAAGCG | 317 |
rs556184500 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647255 | ACCCCGTCTGTACTA[-/A]AAAAAAAAAAAAAAT | 317 |
rs556243281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98678885 | TGAGCATAGGAGGGA[A/G]GCCAAGGGGGTGCTG | 317 |
rs556326689 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98723019 | TCAATTTACATAACC[A/G]CAGCTTCTGTCTGTA | 317 |
rs556335001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731418 | CTTAGTGACTGAAAA[C/T]AAATGAATCTCAGGT | 317 |
rs556375636 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98662912 | CATGAACATCCAAAA[A/T]CTTTTCTGGGAGATT | 317 |
rs556404854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98655973 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCGTGT | 317 |
rs556434136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663576 | ATATAGAAGCTTAAA[A/T]TTTTAAACAGTCAAA | 317 |
rs556492585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657080 | ACATTTCTTAACTCT[C/T]CCCTGATTACAGGCT | 317 |
rs556515442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708761 | GAATTTTCTATTCAC[A/G]GTTTTTCTTGTTTTT | 317 |
rs556536109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704155 | TTTTAATAGAAATGG[G/T]GGTCTCACTGTGTTG | 317 |
rs556548243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697466 | TGTTAAAGATGATAA[A/C]CCCTTGCTGTGTCAC | 317 |
rs556548626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704768 | GAGACTTTGAATTGG[A/G]AGTGTTTTGTTTTGT | 317 |
rs556588343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656563 | CATGCAGTCACTATT[C/T]AGTACATTGCCAAAT | 317 |
rs556612460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698311 | TCCCACCTTGGCTTC[C/T]CAAAGTGCTGGGATT | 317 |
rs556613130 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98649099 | TTATTTTCCAGTTCT[A/G]TGTGTTTATAGAGTT | 317 |
rs556651229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660583 | CAGCAGTTTAGTTGC[C/T]GCTTGTCTTAAGAGT | 317 |
rs556673660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98712725 | CCCTGTGTTGCCCAG[A/G]CTGGTCTCAAACTCC | 317 |
rs556695839 | in-del | -/GTT | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98666849 | TGAGAGTACTTGGTG[-/GTT]TTTAAAAAATTTTTT | 317 |
rs556752448 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692862 | ATATACAAGTGCATG[G/T]GTCTTTTTGGTAGAA | 317 |
rs556756434 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728009 | TAAATAAAAAGGAAA[A/G]GAAAAAAAAAGGCAG | 317 |
rs556772225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674792 | TATATGTATATAAAC[A/G]TATAGACATACATAT | 317 |
rs556833576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666767 | TGTTTTTCCTGACTA[A/G]ATTGAAGTTATAGAT | 317 |
rs556846260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98716809 | GTTAGATCTCCCGGA[C/T]TGATAATCTAGTTTT | 317 |
rs556872083 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674353 | GTAATAGGATGTAAG[A/G]TGAAAAGTCAAAGAC | 317 |
rs556910803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98665998 | ATTTCTGTGGTTCTA[A/G]TGCAGCTGAAGAAGC | 317 |
rs556912938 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704745 | TGTGGGCAGTGTTTT[C/G]TTGGGCAGAGACTTT | 317 |
rs556935599 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653283 | CAGATAATATAAGAG[A/T]TCTAAATTTGATTAA | 317 |
rs556941382 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98671857 | AAGCATTCTTACTTA[C/T]TGAAAAGTTCTAGAG | 317 |
rs556965592 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98651982 | GACACACCCAGCTAA[A/T]TTTTGTATTTTTTGT | 317 |
rs557018066 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650057 | CTGGTAGGTTCTCAG[A/G]GTATTCATCAGGAAT | 317 |
rs557085668 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644499 | CCACAGGAGGCCGGC[C/G]CAGGCAGCCTCGCGT | 317 |
rs557124449 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644810 | TGACCGCGCCCCCTC[A/G]CAGACTTGGCACCGC | 317 |
rs557148770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727025 | GCCACTGGAAATAAA[C/T]GGCAATATTAGTATC | 317 |
rs557182018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661944 | ATAAACAAATTGATT[A/T]AAAAAAACCACTTGT | 317 |
rs557202780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714463 | ACATCCTGGATGTTC[A/G]ATGTTGTTATTCTTG | 317 |
rs557211516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728292 | TAATAATAATAGCAG[C/T]AGTATATGGCTTTAT | 317 |
rs557223549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98649831 | TGTTAACTCTCTGAA[A/G]GGAGGGGATGGATAG | 317 |
rs557229561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659805 | AGAACCATTGCTTTC[C/T]TGCTTTTCTCTCTTG | 317 |
rs557251961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98712062 | TCTCAGGTGGCGGGC[A/G]CAGCAGCTGCTTTTT | 317 |
rs557272864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728884 | TTGTGGTGCTTCAGG[G/T]TCATATTTTTGGTGT | 317 |
rs557318911 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98682864 | TTCATTCATATAAAC[-/AT]GTGAAATCTTGCCCT | 317 |
rs557340144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710829 | CAGACTTCTTTATCA[A/G]CTAGTTCTATGATGT | 317 |
rs557362183 | in-del | -/T | 0.210909 | 0.246925 | intron-variant | APAF1 | GRCh38.p7 | 12:98712825 | TGGCTATTGTATACC[-/T]TTTTTTTTTTGAATC | 317 |
rs557389454 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667973 | AGATGGGGTTTCACT[A/G]TGTTGCTCAGGCTGG | 317 |
rs557424008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661287 | CTCAGTAACTTTTCC[C/T]TAGTTCTACTTTTCC | 317 |
rs557424087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98668531 | AATTTATTATATTTC[A/G]GTGGGTAGTTAAGTG | 317 |
rs557436019 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98653541 | GCATGCCTGTAATCC[C/T]AGCTACCCAGGTGGC | 317 |
rs557446122 | in-del | -/TGCT | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98724314 | CCACCCTGAAGAGCA[-/TGCT]TTCCTCCTCCTCCAC | 317 |
rs557464281 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698928 | AGAGTCTTGCTTGTC[C/T]CTGTTTTCAGAGACT | 317 |
rs557495421 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735754 | AACACAGGAGTGAGC[A/G]AAACAAAAGTCTTGC | 317 |
rs557559886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664496 | GTCTTTTAGAACAAA[G/T]ATTTAAAAAGTTGAG | 317 |
rs557573907 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98657410 | GCTGGGAAGTGGAAT[A/C]GGTATTTGCTCCTCA | 317 |
rs557610457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731735 | TTGTCTCTTGCCCCC[A/G]TTTTAGCTGTGAGAT | 317 |
rs557641952 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709042 | GTGCAAGGGGGATGA[A/G]CATATGGAAGCATTT | 317 |
rs557644456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675937 | GCACCTTTATGTGTC[A/G]GGTGCTGTTTAGAAT | 317 |
rs557714992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98686458 | TAATGATTCTAAACC[A/G]CTCCGTTGAAATAAG | 317 |
rs557768062 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696064 | GAGAGAAAAATTCCT[A/C]TTACTATTGTTTACC | 317 |
rs557816112 | snp | A/G | 0.00731681 | 0.0600405 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644492 | AGGGGGCCCACAGGA[A/G]GCCGGCCCAGGCAGC | 317 |
rs557879439 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98672947 | TTTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 317 |
rs557922358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98709064 | GAAGCATTTTTAAAA[A/G]GGAAGGATTCCAGGG | 317 |
rs557985178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98687130 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 317 |
rs557992597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682000 | TTGTTGTTATATGGC[A/G]TAGACTGCTTAGTTG | 317 |
rs558023855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650079 | ATCAGGAATAGTTGT[A/G]TAGCTCCATCAGTTC | 317 |
rs558043519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679195 | GGGCTTAGCCAGTGC[C/T]GAGCAGACACTGGGA | 317 |
rs558072674 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98650961 | TCCCCATTTAAATTG[C/T]TCTACATTATTGTGA | 317 |
rs558088678 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672777 | TATTTTTTTTGAGAC[A/G]GCGTTTCACTCTTGT | 317 |
rs558177221 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98667287 | TTTTTTATTTTTTGT[-/A]AAAAAATTAAATATA | 317 |
rs558244733 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98699693 | ATTTTGGGCAGTCTT[C/T]CTAACCTGTCATGGT | 317 |
rs558264298 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733968 | TTTAAAAAGCAGTTT[C/T]TCCACTGCTAAATGT | 317 |
rs558298604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98657922 | CCAATAAATATCTGA[C/T]GTAAATAGATCTTTG | 317 |
rs558327705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726349 | AAGAATTGGGGAGCC[A/G]ATTGGAAAAGTTTGG | 317 |
rs558342846 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714023 | GATAAAGTACATCAT[A/G]GATATGTATTTCTTA | 317 |
rs558361071 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652905 | GCTGGTATTACAGGC[A/G]TGAGCCACTGTGCTC | 317 |
rs558374045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709800 | GAACTGGTGGGACAT[C/T]CTCCCTTGCCCTGAG | 317 |
rs558375256 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98656708 | GCCTTATCTGAAACT[A/G/T]GGCAGTTTCCTGAGT | 317 |
rs558408541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653473 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 317 |
rs558434534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661191 | CAGGCGTGAGCCACT[A/G]CGCTCGGCCCCTCCT | 317 |
rs558461838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98703178 | CCTTTATAGAAAATA[C/T]GTTTTAAGATGAGCA | 317 |
rs558462286 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98654197 | GGTTAGAGATTTACA[C/T]ATCAGATGGTCATTT | 317 |
rs558503000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98691481 | TGGGCTTCTTAAGTC[A/G]TCTATACTTGCCTCT | 317 |
rs558527396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707609 | CCCTGGCTGGTCCCC[A/G]CAGCATCCTAATACA | 317 |
rs558724107 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729631 | TCTGAAAGCTTTTTC[A/G]TTCAAAATTGATTCC | 317 |
rs558747979 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | APAF1 | GRCh38.p7 | 12:98694152 | AAATTTAAATATATG[A/G]CCTCAAGCTATTAAA | 317 |
rs558756316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678384 | CTCTGTGGAGCTGGC[A/G]GTAGCTGGGGACAAG | 317 |
rs558773342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98713436 | GGGGAATATGGGTGC[A/G]GGGCTGCCTGTGCTT | 317 |
rs558785613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705725 | AAGAGAAATGTGTAC[A/G]TGTTACAATTATTGT | 317 |
rs558854990 | snp | A/G | 0.000115326 | 0.00759274 | intron-variant | APAF1 | GRCh38.p7 | 12:98706439 | TTTTTGCTCTCTTCA[A/G]AATGCTTATGTATGT | 317 |
rs558878046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663508 | CATGAGTCACCATGT[C/T]CAGCCTGTTACCCAG | 317 |
rs558897231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722907 | TGGCATATTGTGTGT[G/T]TTTTTTTTTCTATCT | 317 |
rs558900529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715873 | AATTTCTCTTTATTT[C/T]TCTTTACAGTAGTAA | 317 |
rs558979913 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98670341 | TACCGGTGAGATTTT[A/G]GCCATCTGTGCTTTT | 317 |
rs559013737 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679279 | CTGTGCAGATGACAG[C/G]AGGACCAGCTGCAGA | 317 |
rs559074077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717120 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 317 |
rs559134996 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98669687 | AAGCATATTCATCTG[A/G]TTATTTTCTTAGGAT | 317 |
rs559135967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709398 | AGTCCCAAAGATCCA[C/T]TGGCAGAGGAATGGT | 317 |
rs559146420 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98717932 | TTTTGTCTTGGTCTC[C/T]TCAGATTCCTAGAGA | 317 |
rs559147388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696571 | CAGAGCTGTATGTGT[G/T]CTCTGCATCTTTAAC | 317 |
rs559218137 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643661 | TTTAAGTGAACACAA[C/G]TGCTATGTTTTTGTA | 317 |
rs559229143 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685674 | AGAGTCTTCCTCTAT[C/T]ACCCAGGCTGGAGTG | 317 |
rs559259505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710169 | GTGAGCCACCGTGCC[C/G]GGCCTAAGGGTTTTT | 317 |
rs559261786 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659581 | ACATGGTGAAACCCC[A/G]TCTCTACTAAACATA | 317 |
rs559303001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695774 | AAGATTCCTCTTGAC[G/T]TAGCTTCACCTTTAT | 317 |
rs559362076 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98676151 | TAACGTATATGAAAT[-/TC]TCTGTCACTGCACTA | 317 |
rs559412551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660017 | TCTAATGGGTTAACA[C/T]AGAACAACAGAGAAT | 317 |
rs559424959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652159 | GTTTTTGCTATCTTG[C/T]CCAGGCTGGTCTCAA | 317 |
rs559454716 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98688464 | CCTTCTACCACTGTT[A/T]TCTTTCTTTTTTTTT | 317 |
rs559484281 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734139 | AGAGAATTCTCTGGT[C/T]TTCTGTGTAATTCCA | 317 |
rs559528579 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98664782 | TCAAGCAATCCTCCC[A/T]CCTCAGCCTCCTGAA | 317 |
rs559596107 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706421 | TTCTTGCTATTTTCA[A/G]TATTTTTGCTCTCTT | 317 |
rs559596881 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98647633 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 317 |
rs559628432 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703344 | AAAGTATTTTACCTT[C/T]ATAGGTATCTCTATT | 317 |
rs559688526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658271 | GTAAATAAAAATACA[C/T]ATTTCAAGATGTTTT | 317 |
rs559705068 | snp | A/C | 1.90871e-05 | 0.0030892 | intron-variant | APAF1 | GRCh38.p7 | 12:98649700 | GTAAGTGTCTTAGTC[A/C]ATTTCATAGTCTAGT | 317 |
rs559743585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662348 | CCATCTATTTGTTTT[A/T]AAAAAAATTTAATTT | 317 |
rs559759971 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691090 | CGCATGCCTGTAATC[C/G]CAACTACTCAGGAGG | 317 |
rs559806393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663004 | ATTAAAATAATATTT[A/G]CCATCTACCCACAGT | 317 |
rs559814017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675158 | CTTTATTTAAGTACT[A/G]GAAACTTTTTTGGTG | 317 |
rs559834927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727569 | AAAAAAAAAATCTGG[C/T]AGTAAAATGAGTTTA | 317 |
rs559923866 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704435 | ATCAAGGGAGCCATG[A/T]CTACTGCAAGCACTT | 317 |
rs559935831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657281 | AGTCCTCTCCTAGAC[G/T]TCAGCCATCATTGTC | 317 |
rs559964806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680770 | GGTTGATCACCTCAG[A/G]ATTAAACAAGCAGTG | 317 |
rs559990173 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718118 | CCCTCAGTTGTGCTG[G/T]TGCCCTTAAATTCAG | 317 |
rs559993985 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731814 | ATAAGCAAATTCAGT[A/G]ATTGGGAAGGAAAGG | 317 |
rs560034345 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | APAF1 | GRCh38.p7 | 12:98647273 | AAAAAAAAAAAATAA[A/G]ACAAGGTGGGGGAGA | 317 |
rs560035307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718756 | CCTGGGCAACATAGC[A/G]AGACCCCATCTCTGC | 317 |
rs560056100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98723117 | ACTTTAGACAAGAGA[A/G]TGTACACTCTCTCCA | 317 |
rs560118532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670487 | ATTTTCTATAAAAAT[A/G]AGGATTGAAGCCCTG | 317 |
rs560139199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98677885 | TGTGATTAAAAAACA[A/G]TGATTAGGAAAATAC | 317 |
rs560200263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98670028 | GAAATCACTGCAACC[A/G]CCACTTCCTGGGCTC | 317 |
rs560213908 | snp | C/G | 3.29533e-05 | 0.00405901 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715520 | GCCGATGAGAAGACT[C/G]TTATTTCAAGTTCTG | 317 |
rs560252704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732119 | GAGAGTTGAGTCTGG[C/G]CACTGCTGTAATGGA | 317 |
rs560358634 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98724312 | CACCACCCTGAAGAG[C/T]ATGCTTTCCTCCTCC | 317 |
rs560369987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692625 | TGTTTAGCTCTGGCT[C/T]ATAAGTGAGAACTTG | 317 |
rs560410121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98678514 | GGCCAGAGCCCTGCC[C/T]TCCTGGGTGTAGCTG | 317 |
rs560431664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98684644 | ACTGGATTGGACCAA[A/G]ATTACAGAGTAATGT | 317 |
rs560434891 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674774 | GAGGATTAAATTAGT[G/T]TATATATGTATATAA | 317 |
rs560444742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731007 | GGAATACATGGTGAT[A/G]AATGGTGGTGTGCCA | 317 |
rs560450850 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722023 | CTTCATCAGGCCCAC[A/G]GGGCTGTTTCTTTGG | 317 |
rs560528912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689976 | TTGACATCTTTTTGT[G/T]GTATTATACCTTTCT | 317 |
rs560547248 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697060 | CTACAACCAGATTGA[A/G]CTTGTTCTTCTTTTT | 317 |
rs560584491 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694589 | ATTCTTGTGTGATTA[C/G]TTCCTTTTAAATATT | 317 |
rs560595532 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711063 | ATTTTACAAGTTTTA[C/T]TATTGTCCTCAATAT | 317 |
rs560660849 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731298 | GCATTTGTTACAATT[A/G]ATGGATCCACATTGA | 317 |
rs560675679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724988 | GTAATTTCACTCTCT[A/G]TAATCTCATTTAATC | 317 |
rs560710807 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | APAF1 | GRCh38.p7 | 12:98684578 | TAGTGCTCTTTAGGC[A/G]TATTTATGTTTATAG | 317 |
rs560774539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98700844 | GTATTTCATATAAAT[A/G]GAATCATATAATATC | 317 |
rs560785006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659881 | GCTTTTTCTCTTTGC[A/G]TGCTACCTACCACAT | 317 |
rs560801783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694355 | AATGGTGGCTTCTTT[C/T]AATCTGGAAACTTAT | 317 |
rs560805735 | snp | A/C | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735809 | GAGGCAGAAAAAGTA[A/C]ATAAGTAAAATCTAT | 317 |
rs560815444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697525 | TCGGACACTTTTTAA[A/G]AAGTCATCATTTGAC | 317 |
rs560868612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728375 | TAAATTTCATTCTTG[G/T]TTTACAGATGAGGAA | 317 |
rs560905576 | snp | A/C | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644369 | AAGGGAAAAACAAGG[A/C]TGGGCTGTTTCCTTC | 317 |
rs560946627 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709154 | GTGAAAGGAGCTGGG[C/T]TTTACATACTGAAGT | 317 |
rs560979126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98707262 | TTCCTACAGGGAACC[A/G]ACACTGGACTGCTCA | 317 |
rs561040529 | snp | C/T | 0.000197173 | 0.0099271 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644540 | GGCCAGGCCCAGGCA[C/T]GTCCCCAGCGACAGC | 317 |
rs561116265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705894 | TGCATGATTCCAAAG[A/T]CAAAGTTTTATAATG | 317 |
rs561168031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721167 | GCACAGTGTGTTTCC[A/G]TGCAACAACAACAAC | 317 |
rs561169808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713144 | TTTTATACTAAATAA[A/C]TCTTTCTGTGATCTA | 317 |
rs561174454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98651388 | GTTGTTGGTATGCAG[A/G]TATTTTAAATTTGCA | 317 |
rs561211016 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644041 | AGGCTAGTCTCGAAC[C/T]CCTGACCTCAAGTGA | 317 |
rs561224847 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645476 | AAGGGCGCCACAGGC[C/G]GGGAAGACCTCCTCC | 317 |
rs561280883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713757 | ATTACTTATGGCACT[A/G]GCCACAGTTATTTTA | 317 |
rs561360208 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678929 | ACTGGCCTGCAGGCT[C/T]CCCTTGGCACCTACA | 317 |
rs561397043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683823 | AACTCTACTTGAATC[A/G]TAAGTAGAGCTTAAT | 317 |
rs561397952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699874 | ACAATTTATGCCATC[A/G]AATCCAGTGTTCCTC | 317 |
rs561493973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667836 | GAGTGCAGTGGCACA[A/G]TCTCAGCTCATTACA | 317 |
rs561504142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724033 | TGTAGGCAATAAAAA[A/T]CATTGAAAAGCATTT | 317 |
rs561566651 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648717 | ACAATGCTCTACTAC[A/G]TGAAGGATATAAAGA | 317 |
rs561567252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716303 | TCCTGCCTTCAGCTT[A/G]TGTGCATGCACACGT | 317 |
rs561569053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661381 | AGACTAGCTTACAAA[G/T]CCAGGCATATTTTTT | 317 |
rs561569072 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681675 | TTGATAGATTGGACT[C/T]GTGGCTTAACCAACA | 317 |
rs561590804 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653393 | TGGGTGTGGTGGCTC[A/G]TGCCTGTAATCCCAG | 317 |
rs561595989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702454 | GTATATTGTATCAAT[A/G]CATGTAGTAAATAAA | 317 |
rs561616927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668690 | CAAAGATGACTCAAA[C/T]CCCAGTGGAAAGAAC | 317 |
rs561627429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653194 | AATCTCTGGAGTTCA[C/T]TTCCATTCTCAAATA | 317 |
rs561639295 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660795 | TGCACTTTTTAAAAA[C/T]GCCCTAATGCACCCA | 317 |
rs561643253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650200 | TTCTAGTAGTTAATA[A/T]TTTTTTTTTTAGTAG | 317 |
rs561681794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717112 | TGACCTTGTGATCCG[C/T]CCGCCTCGGCCTCCC | 317 |
rs561730287 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98702223 | GGCACCTGCCACCGC[A/G]CCCGGCTAATTTTTT | 317 |
rs561773950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665484 | TTAGTAATGTAAGTA[A/G]GTAAGTCGATTCTTA | 317 |
rs561799415 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666484 | GCTTCCCCTAATATT[A/G]ACATTTTATATAACC | 317 |
rs561851429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670892 | TTACTGTTTCTCTTA[A/G]CAGTGTGAGGTTAAT | 317 |
rs561851503 | in-del | -/CCTC | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98724320 | TGAAGAGCATGCTTT[-/CCTC]CTCCTCCACTGGTGA | 317 |
rs561862594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708503 | CATAGGTATTTTATG[A/T]GAAACATAGTTTGTC | 317 |
rs561871021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659108 | CAGTAAAACCATTTA[A/C]AGGAGTACTCCTGTT | 317 |
rs561905476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679237 | AGAGAGGAGCAACCC[A/G]CTCTAGTGCCCCCTC | 317 |
rs561924558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98672559 | CACTGAACCCTGATT[A/T]TTCTGTCTCTTAAAG | 317 |
rs561958857 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694011 | AGTTTAACAAGGCCA[A/T]CAAAAGCAATGCGGG | 317 |
rs561961409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710481 | GAGAGAGGAGCAGAA[C/T]AGAGAAGACGAGAGT | 317 |
rs562017726 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | APAF1 | GRCh38.p7 | 12:98665144 | AAGCAATCCTCCCAC[C/T]TCAGCCTCCTAAGTA | 317 |
rs562023461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726419 | AAGATGGGGTTTTCC[C/T]CCTTTCATTACAAAG | 317 |
rs562039927 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98719955 | GAGTCCTAGGAAGCA[-/G]TATGATTGCAATGAA | 317 |
rs562044252 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672912 | GGCATATGCCACCAC[A/G]CCTGGCCGATTTTGT | 317 |
rs562116231 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733158 | TTTTGTTTTTGGAGA[C/G]AGAGTCTTGCTTTGT | 317 |
rs562117411 | in-del | -/CAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721170 | CAGTGTGTTTCCGTG[-/CAA]CAACAACAACAACAA | 317 |
rs562125951 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663686 | CTCTTTTGAGACAAG[C/T]CTCACTCTGTCGTCC | 317 |
rs562151315 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670116 | CACCCGGCTAATTTT[A/T]GTATGTTTTGTAGAG | 317 |
rs562183769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98679928 | CCAGGCTGGTAGTGT[A/G]AGCTGAATGCAGCCT | 317 |
rs562190950 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714801 | CATATTTCCTCTCTT[C/T]TTGTTTTTTTGGTAT | 317 |
rs562194819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669087 | GCAAAATATATTTAC[A/G]TTTAATAGTGTATAT | 317 |
rs562259504 | in-del | -/GTATGACAGAGCAT | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98668573 | ACAGAGCATGGAAGG[-/GTATGACAGAGCAT]GGAAAGAAAGTGATG | 317 |
rs562259944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98681180 | GATTCTTATGCCTCA[A/G]CCTCTTGAGTAGCTG | 317 |
rs562294713 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734041 | AGATTTTTCTAAGAA[A/G]TGTGAAATAGAACAA | 317 |
rs562360698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680645 | AAACTCCAATTCCTG[G/T]GCTCAAGTGATCCTC | 317 |
rs562392155 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98682255 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 317 |
rs562393330 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733539 | CTGGGTTCAAGCAAT[A/C]CTCCTGCCTCAGCCT | 317 |
rs562416934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725932 | TTCTGCTTTTTCTGT[G/T]CTGAAAGAAAAGATC | 317 |
rs562424947 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98721589 | CCCTTCCCCCAGCAT[A/G]TCTCATTGGGTTCTT | 317 |
rs562427138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729743 | GATAAGTGTTTGGAA[A/G]TATTTGAATGACTGG | 317 |
rs562427277 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712235 | CTGTGTTTTATTTTA[-/T]TTTTTTTCAATTGAA | 317 |
rs562465554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98662314 | TAGCAAAGAGGAAGA[A/G]TCATTTTCCTAGATC | 317 |
rs562476249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714861 | TTTTTTTTTTTGACA[C/T]AGTCATTATCTTTTG | 317 |
rs562553520 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98677710 | GTTTCTCTAGAGATT[A/T]AAAAGATACAGTTAC | 317 |
rs562563854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661489 | TATTTTTATTTTTAT[C/T]TTTTTAGATGGAGTT | 317 |
rs562611425 | snp | C/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98683947 | TAATGTTTGATTGTA[C/T]CTTTTTTTCCTCTTA | 317 |
rs562612565 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686970 | TTCACATTTCTACAG[A/T]AAGAGCCTGCTTCTT | 317 |
rs562620745 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679336 | TGAACACTTGTCAGG[A/G]GGACTTGCCTAGCAG | 317 |
rs562667179 | snp | C/T | 2.18672e-05 | 0.00330653 | intron-variant | APAF1 | GRCh38.p7 | 12:98699385 | AAAACAAACTTTTTC[C/T]TTTTTATTACTTTAA | 317 |
rs562681565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98691931 | TCATCTTTTTTCAGG[C/T]ATGTCATCTGCAACC | 317 |
rs562687972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723400 | AGCCACTGTGAGGCT[A/C]ATTACTTACTTAAAA | 317 |
rs562698486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690868 | CCCCCTCAGAAATTG[A/C]TGTAAAAAGCCTCTG | 317 |
rs562710823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98683044 | AATCTGCTATGACAG[C/G]ATAAGATAGCATTTG | 317 |
rs562781939 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674031 | AGACAGGACCTCACT[A/T]TGTCATTTAGGTTGA | 317 |
rs562810601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700695 | CACAATGCTGTGTAG[C/G]CATTACTACTATATA | 317 |
rs562814194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98678621 | CTGTAGCTGCCCAAG[C/T]GGTGGCTGCAGACTC | 317 |
rs562818391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98691876 | TACCACCTCTATCAC[C/T]GCTCTTCCATCCCAG | 317 |
rs562876662 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669200 | TTTTTGGTCCTTATG[A/C]TGTAATGAGCATTCT | 317 |
rs562933776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707091 | GCATGCAGCTTCTAA[A/G]ATATTTTTTTTTCAT | 317 |
rs562974821 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660684 | CCAACATTGAGTGTT[A/G]TGCCAGGTTCTGGGC | 317 |
rs562976615 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | APAF1 | GRCh38.p7 | 12:98655358 | GGCACACCTCCCAGA[C/T]GGGGTGGTGGCCGGG | 317 |
rs563089249 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735063 | GTCCAGCCTGGGTGA[C/T]ATAGCAAGACCCTGT | 317 |
rs563089259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726684 | CTCCTTTCCCAGTTA[A/T]GAGGCGGTGTTTCAT | 317 |
rs563194062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656078 | ATGAGCCACCGCGCC[C/T]GGCCTTGCCTGGCTA | 317 |
rs563229831 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643926 | GTTCAAGCGATTCTC[C/G]TGCCTCAGCCTCCGG | 317 |
rs563277561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703574 | AATGGGCAGCTTAAA[C/T]CATTAACTGCTGAGG | 317 |
rs563354847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710967 | GATACTGGGAGTAAA[A/T]CGCCTGGTATGTGGT | 317 |
rs563380073 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704030 | GTTCAGAATGTATAC[C/T]TAGCTGGCCCTGGAA | 317 |
rs563429606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659040 | TTCTACTCTAAATCA[A/G]GAGAAGTTGAAGATG | 317 |
rs563451777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710354 | TTGGCAGTGATAACA[C/T]AGTCTTATGCCATCT | 317 |
rs563457319 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98645046 | GGGGTCGCGCGCGCC[A/C]CGTCGGGCGCGCCGC | 317 |
rs563478026 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701445 | TTCCACAGCAGCTGC[A/G]CCGTTTTACATTCCA | 317 |
rs563491267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713042 | CAGGCTGGCCTTAAA[C/T]TCTTGGGCTCAAGTG | 317 |
rs563532576 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98658378 | AATATTGGTAAGTTG[C/T]TCTCAGATCCATAAC | 317 |
rs563554635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650496 | CATCTCAAAAAAAAG[G/T]TTTTTGTTTTTTTTT | 317 |
rs563583136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98651273 | TTTCAAAATTTCCTA[C/T]TCTTATTTCCTTTCC | 317 |
rs563630126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704511 | GCCTTGCCCATTACT[C/G]TGAAGGTGTTGGGGG | 317 |
rs563692514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705191 | TTTCTTGTCACTTCT[A/G]AAGTCCTTACCCTCT | 317 |
rs563770967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664027 | TTTATTTATTTATTT[A/T]ATTTATTTTTTGAGA | 317 |
rs563838198 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676323 | CAAGCGATTCTCATG[C/T]CTCAGCCTCCCGAGT | 317 |
rs563859837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98674404 | TCCCACTTTCCAGAG[C/T]TGACCATTCCTTAAT | 317 |
rs563907822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731124 | CACTCATTAGCTTTG[A/T]GACCTTGCACAAGAT | 317 |
rs563926774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719495 | GCTGGGACTACAGGC[C/G]CGTGCCACCATTTCC | 317 |
rs563933326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667227 | CTAATTCCCGAGTAG[C/T]TGGGTCTGCAGGCAT | 317 |
rs563990765 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667592 | ATCAGGAAGACTGTA[A/T]GTATTGGTACAACTT | 317 |
rs564063315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716278 | GTTGCTTTTTTCCGC[C/T]TTCCACCTGTCCTGC | 317 |
rs564265584 | snp | G/T | 0.000399281 | 0.0141238 | splice-donor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98715554 | ATGCTGAAATTCAGG[G/T]GAGAGGGAGGATGAA | 317 |
rs564291645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685828 | TTTTAGTAGAGATGG[C/G]GTTTTGCTATGGTGG | 317 |
rs564319213 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98678557 | CCACAGCTGCAGGCT[C/G/T]GGGCCTCCGGCTCCA | 317 |
rs564331748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670616 | ATGTAGTTAAATACA[C/T]TTTTATATAGTTAAG | 317 |
rs564355224 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98718296 | GGAGTGCAGTGGTGC[A/C]ATCTCGGCTCACTGA | 317 |
rs564383167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664862 | TTTTCTATATCTTGA[A/G]CATTTTCCCATGTTG | 317 |
rs564439343 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658597 | AACTTCCTATTTTAA[A/G]TCTGTATAAGAAAAC | 317 |
rs564440712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725068 | GCTATAGAAGCTTAT[A/G]TGAGTTGTCCTAGTC | 317 |
rs564446637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723932 | GGTATCAAATGAATG[A/G]AATGAAATACATTGA | 317 |
rs564532243 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | APAF1 | GRCh38.p7 | 12:98686898 | TGTACACTATTAAAA[C/T]AGGTTGTATTTTATG | 317 |
rs564549916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725890 | TAATTTTGTAAATTA[C/T]GGTCTGGATTATAAA | 317 |
rs564554146 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697765 | TGATGTTAGATAACA[C/G]CATTTCAAGGTCAAA | 317 |
rs564591666 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98677008 | CAGTTAGGAAATGAG[C/G]ATTTTGCTATGATTT | 317 |
rs564714596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694984 | TGATGTCAAAGTCTT[G/T]ATATCTTTTGTCTTG | 317 |
rs564727447 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734273 | TTATCTCCAAGGTTA[A/G]TCAGGAAAAATAGCT | 317 |
rs564776669 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709387 | AAGAGAGAAGGAGTC[C/T]CAAAGATCCATTGGC | 317 |
rs564803343 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707226 | ATGGCCTTATTCTGC[C/T]CCACTCTGTCTCCCA | 317 |
rs564846095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98668874 | TCTAGAATTCTGGGG[A/G]GAATTATAGATGAAA | 317 |
rs564951561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668031 | TCAAGTGATCCACTC[C/G]CTTCAGCCTCCCAAA | 317 |
rs565005337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98686019 | AGAGATCTTAAATAT[A/G]AATACTATGTTTATT | 317 |
rs565029751 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644955 | CTTCCACTGCGATAT[C/T]GCTCCAAATCCGAGG | 317 |
rs565048639 | snp | A/C | 0.000200398 | 0.0100079 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644565 | GACAGCAGGCTCAGG[A/C]ACGTTCGGGGGTCTG | 317 |
rs565088456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697627 | AGCAGGGGACAGACA[C/G]TACTGCACTCTTGGT | 317 |
rs565090645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713902 | TCTCAATACTCTTAT[A/G]TATTTGTCATGGCCC | 317 |
rs565098117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98690102 | TTTGTTTGTTAGAAT[C/T]TCTAGGGAAGGAGAT | 317 |
rs565172834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656535 | TCCAGTTGTTTGTTA[C/T]ATTTTAGACTTTCAT | 317 |
rs565236190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646678 | TTGAATGAATGAATT[A/G]ATAAACCCGTTTAGA | 317 |
rs565352411 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98693352 | TTTGGCCTCAGCCTC[C/G]CAAAGTGCTGGGCTT | 317 |
rs565352941 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98684744 | TGTACCACTAAAAAA[A/C]AATAAGACTGTTATA | 317 |
rs565488585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714645 | CATTTAGGAAGGTTT[C/T]CATTCACACAATTCC | 317 |
rs565500042 | snp | C/G | 3.31301e-05 | 0.00406989 | intron-variant | APAF1 | GRCh38.p7 | 12:98708576 | ATAATTTCTTTATCT[C/G]TTAATCAGCTCTGGG | 317 |
rs565512048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98653784 | TCTTTTGAAATTTCA[A/G]TGCTTTAATTTTTTC | 317 |
rs565570770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653858 | CAGTAGTGACATTTT[A/T]CATTACTGTATTCGT | 317 |
rs565571159 | snp | A/G | 1.66156e-05 | 0.00288228 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732396 | ATTACCAATCTAATG[A/G]GAATTTTATTTTTCT | 317 |
rs565582751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654748 | AATTTAAAAAAATGG[A/G]AACTTAAGGCAACAG | 317 |
rs565597531 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645567 | GCTCCGGGACTGTGG[C/G]GTCAGGCTGCGTTGG | 317 |
rs565600799 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650297 | AGACCAGCCTGGGCA[A/G]CATGGTGAAATCCCG | 317 |
rs565689665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98687673 | ATTCATGAGGGTAGC[A/G]CCCTCATGACCTAAT | 317 |
rs565752582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679963 | GGCCAAGTGGGTGAA[A/G]CAAGACCAGTGGGCC | 317 |
rs565827881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651575 | CCAACTCTCTGCTGC[C/T]GCAGCAAAGCTGGGT | 317 |
rs565912341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656883 | AATGCTTTGAGGTTC[A/C]TGTCTCTAACCTTTC | 317 |
rs565949071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98648838 | TCCATTATACCTTCT[A/G]TCACTTTGCTATCAA | 317 |
rs565979363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700916 | AGGTTCATTCATGTT[A/G]TAGCATGTATCAGAA | 317 |
rs565989451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657826 | AGTTTCCTCATTTTC[A/G]AAATGAAGATAATAG | 317 |
rs566038436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703144 | AGGCTAGCTTGAGAG[C/T]TCATCTGTGATGAAT | 317 |
rs566041492 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670695 | AAGATTTCCTTCACT[A/G]CAAGCTTACAAAAAT | 317 |
rs566049514 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98658717 | GGAGACATTTTTGTT[A/T]GTCAGTACTGGTGAA | 317 |
rs566075556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696778 | TAGGATTACAGACAT[G/T]AGCCACTGCACCCTG | 317 |
rs566087000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98696267 | CTCATGGTGGAAAGG[A/G]GAGGGGAAGTGGGCG | 317 |
rs566101820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703851 | TAAACAGTGTAGGCA[C/T]AGACTCTTTTCTTCT | 317 |
rs566104290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726018 | CTGTGGACTGCCTGC[C/T]TGTTAAACAGTGCAG | 317 |
rs566220586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98655480 | CCCCCACCTCCCTCC[C/T]GGACGGGGCGGCTGG | 317 |
rs566229691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717438 | TGGAGTGCAATGGTG[C/T]GACCTTGGCTTGCTG | 317 |
rs566266154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98692363 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 317 |
rs566284383 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679572 | TGCCCCTTGCTTGCC[A/G]CATTGCAAGTGAAGA | 317 |
rs566284705 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98693898 | AGTAAATTTTTAAGG[G/T]GTCTTTATTATAATG | 317 |
rs566415906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710572 | GGTAGGACAGAGTTT[A/G]ATGAGTTGTCATTCA | 317 |
rs566429449 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645769 | TTTCCCTCCACCGGC[C/T]TGGAGTCTCCCAGTC | 317 |
rs566445624 | snp | C/G | 0.000131807 | 0.00811701 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715516 | CACAGCCGATGAGAA[C/G]ACTCTTATTTCAAGT | 317 |
rs566445699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661637 | TGTGCCACCTCGCCT[A/G]GCTAATATTATATTA | 317 |
rs566469180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680460 | TCATTTTATTTTTCC[A/G]TGATCATGAGACCAG | 317 |
rs566475366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98707296 | TTTCCCAAACACTCC[A/G]TAGTTCCCTGCTTCT | 317 |
rs566529718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676546 | AGCAGTAATATAATA[C/T]CTATACTGGTGGAAT | 317 |
rs566588452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700219 | GGTTACAGTAGCCCT[A/G]TGATAATAATGAGGC | 317 |
rs566603899 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98715819 | CTGTCTTGGTATTTG[A/G]ATTTGTATCAGTAAG | 317 |
rs566623885 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98729286 | TTTCCTTGGAAGACA[A/G]TTTTTCCACAGATGG | 317 |
rs566634199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720945 | ACACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 317 |
rs566669375 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652564 | TTTTTTTCTTTTTGC[C/T]TTTTAGGAGTTTCTT | 317 |
rs566713479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669103 | TTTAATAGTGTATAT[C/T]GGAATGATGGTATTC | 317 |
rs566726846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98685013 | CTTCATGTAACTTGC[C/T]TTATCTGAAGAATTG | 317 |
rs566732602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670268 | ATTCTTGTTACTCCT[G/T]TAGTCTTCAGAAATC | 317 |
rs566748755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713310 | CACATATATCAAATA[C/G]TATCTATCAAGATTT | 317 |
rs566788770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98685941 | CATGTCCAGCCTGAA[A/T]AGAGGATTTTACAGC | 317 |
rs566809788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721778 | GCTTGTTGGGGAGGA[C/T]GACTGCTAAATGTGG | 317 |
rs566810062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714319 | ATAATACATAATGAA[A/C]CATGTGAAATTACCA | 317 |
rs566867611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98663957 | GCTACCATACCTGGC[C/T]ACCTTATTTTTCATT | 317 |
rs566885966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718391 | GCACCTGCCATCACA[C/T]GCAGCTAATTTTTTT | 317 |
rs566898819 | snp | C/G | 1.6698e-05 | 0.00288941 | intron-variant | APAF1 | GRCh38.p7 | 12:98670953 | ACAGTGCTGCTGATA[C/G]TACTTTTTGTTTTTT | 317 |
rs566927729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663400 | AACTTAAAATTTATA[A/T]ATAGAATCTCGCTGT | 317 |
rs567008140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718897 | TATGATCATGCTACC[A/G]CACTCCAGCCTGGGC | 317 |
rs567037482 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719386 | GAGACAGTCTTGCTC[G/T]GTTGCCAGGCTGGAG | 317 |
rs567041527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730492 | GTGACCATATTTGCA[A/G]AGTTCTTGGGGAACC | 317 |
rs567054935 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98722792 | GCCAGCTTCAGTGGG[G/T]CCAGGATCTGTAGAC | 317 |
rs567112163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687888 | GTGATCTTGGCTCAC[G/T]GCAGCCTCTGCCTCC | 317 |
rs567112607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98696010 | GATTTTGTTGCTGCT[A/G]TCTCTTTCTCCATTT | 317 |
rs567124083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726768 | AATTTTTGTTGGTAC[A/C]TTAAAAAAATTTTTT | 317 |
rs567124784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688756 | TGAGCCACCAAGCCT[A/G]GCCTACCACTCTTTT | 317 |
rs567153937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731272 | TATGAACATCCCCCC[A/G]CCAGAGATGTGCATT | 317 |
rs567191434 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | APAF1 | GRCh38.p7 | 12:98689472 | AGAGAGAGTGTGTGT[C/G]TCTGTGTGTGTGTGT | 317 |
rs567207071 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671731 | GGATGTAAGTAGGTT[A/G]GGAGAGAAACCAAAG | 317 |
rs567207749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98689496 | TGTGTGTGTGTGTGT[A/G]AGAGAGAGACACAGG | 317 |
rs567233666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673912 | AAAATGAGGAATTCA[A/G]GGGAGGGTTCCATGA | 317 |
rs567266779 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673713 | CTGTACTGTGCTAAG[C/T]ACTAGCATTTGAGTT | 317 |
rs567381786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667303 | AAAAAATTAAATATA[C/T]GGATATCTCTCTATG | 317 |
rs567383655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659565 | AAGACCAGCCTGACT[A/T]ACATGGTGAAACCCC | 317 |
rs567458422 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734355 | GAACTTTAGTTGAAG[C/T]GTAAATCTAAAGAAA | 317 |
rs567542438 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733797 | TTTTATTGGTCTACC[C/T]TTTTCTCACTGTAGC | 317 |
rs567565341 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684090 | TCTTTGCAATTGAAC[A/C]TGATATTTTTGAGAG | 317 |
rs567571015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672207 | TCTCACTATGTTGCC[A/G]AGGCTGGAGTGCAGT | 317 |
rs567593596 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731413 | AGAGCCTTAGTGACT[A/G]AAAACAAATGAATCT | 317 |
rs567610813 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645148 | AGGCGGGCACTTCTA[C/T]GCGCGCGGGCATGAG | 317 |
rs567642525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698768 | GCTCATGGCCCAGAG[A/G]AGTGAAGGTGGATCT | 317 |
rs567656821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728741 | CAAACAAACAAAAAA[A/C]CCAAAAATAAAGTTA | 317 |
rs567664372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98691076 | GCTGGGCGTGGTGGC[A/G]CATGCCTGTAATCCC | 317 |
rs567677432 | snp | C/T | 9.19853e-05 | 0.00678117 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735536 | CTATTTAGGCTTTAT[C/T]AGCTATATGTAAATT | 317 |
rs567716317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675570 | TCTTTTCTTGTTATT[A/C]TTTCCTAAACACGAT | 317 |
rs567726135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683089 | TTGCTTTGCCCCTCT[C/G]TTCTCCCTTTGAAAA | 317 |
rs567737598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728028 | AAAAAAAGGCAGTTA[C/G]TATTATCCCCATTTT | 317 |
rs567803382 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723473 | ACCTACATCTGCTGT[A/G]TTTAATGAGCATTTA | 317 |
rs567830028 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671562 | AGTGAGAATTTTCAG[G/T]AGTTTTTATCTTTAA | 317 |
rs567874055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98715659 | CACATTACGTTGGGC[A/G]TACATTCAGATTATG | 317 |
rs567875437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98651713 | TTGCCCAGGCTGAGT[G/T]CAGTGGCCATATCAT | 317 |
rs568039883 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98707711 | ATATATATATATATA[C/T]ACATATAAATTTACT | 317 |
rs568056054 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98693796 | CTTGTTTTTCAGTTT[G/T]TTTTTTTTTTTTCGT | 317 |
rs568068477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694608 | CTTTTAAATATTATT[C/T]TGTTCTTGTTTCATG | 317 |
rs568115044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687029 | CTGTAATTGCTTATC[A/G]TAATGATTGTTTATG | 317 |
rs568159183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732323 | TTTGCTTGAGTTCGG[C/T]TGGGGGGAGGAGATA | 317 |
rs568202004 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661696 | CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC | 317 |
rs568203391 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98658529 | TGAGACTGAGGTTAA[A/G]TGATTTGATAAAGAT | 317 |
rs568243504 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98695381 | TTTTTTTTTGAGACA[C/G]GGTCTCACTCTGTCA | 317 |
rs568262422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708051 | TCCCAGGTTCAAGCA[A/G]TTCTCCTGTCTCAGC | 317 |
rs568270389 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726843 | TGTATATGTACTACC[C/T]TACTGAACTGTTTCT | 317 |
rs568353259 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98672272 | CGGATTCAAACGATT[C/G]TCCTGCCTCAGCCTC | 317 |
rs568367007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664166 | TGGGATTACAGGTGC[A/G]TGCTACCTCACCCAG | 317 |
rs568393059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98700946 | ACTGTATTTCTTCTT[A/G]TGGCTGAATAATATT | 317 |
rs568613175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672840 | GCTCACGGCAACCTC[C/T]TCCTCCTGGGTTCAA | 317 |
rs568635846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98667335 | TGCCCAGGCTAGTCT[C/T]GAAGTCCTGGCCTCA | 317 |
rs568638965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699031 | GCATGTGGTAGGTTC[A/G]TGAAACACACTTCAT | 317 |
rs568644449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98724583 | TGAAGCATTATGACT[C/T]ATCTTTCTAGACCTA | 317 |
rs568674551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657090 | ACTCTTCCCTGATTA[C/T]AGGCTAGACCCTGAT | 317 |
rs568717526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98713216 | GGCTGTATATTTTTC[A/G]GATTTCCTTTATTAC | 317 |
rs568756427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716860 | TCTATAGTGTGCTTT[A/G]TGTTTTTTTCTTTAT | 317 |
rs568769593 | in-del | -/ATTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672177 | TTTATTTATTTATTT[-/ATTT]TTGAGACAGAGTCTC | 317 |
rs568777645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705424 | GGCCCTTAGCTCTGT[A/T]TGTCCCAGCTTGGAC | 317 |
rs568784482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98676429 | GGCCAAGCTCATCTC[A/G]AACTCCTGACCTCAA | 317 |
rs568820704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98653338 | TTCTTTGGGTGGTGA[C/T]TGGCATAAATTAAAG | 317 |
rs568884455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98721950 | AGTTGTGGCTGCTTT[A/T]TCTTTATCTTTTTAT | 317 |
rs568884757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730255 | TTCTCCTTTAGTGTA[A/G]AGATAAACTAGAACT | 317 |
rs568964108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98706271 | TTCAGTTGGTTCCCT[A/G]TTGATGAGTATTTAG | 317 |
rs568973668 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645249 | GGGCGCGCGCCGTCC[C/G]GGCTGGGTGGATCCG | 317 |
rs569107734 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682951 | TATTTGCAAATAATT[G/T]TTTTTAAACATTAAG | 317 |
rs569201047 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712807 | GCATGGGAGCTTTTG[G/T]GCCTGGCTATTGTAT | 317 |
rs569221642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729521 | AGCCGCTCACCTTCT[A/G]CTCTGCGGATGGGTT | 317 |
rs569239318 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98719632 | GCTGGGATTACAAGC[A/G]TAAGCCACCACGCCT | 317 |
rs569299970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98715237 | CATACATGGTGTGCA[C/T]ATATATATATATATA | 317 |
rs569315042 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98669472 | CATTTTGCTGCTTCT[A/G]TAAACATACTTGTCT | 317 |
rs569325493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670106 | TGCACCACCACACCC[A/G]GCTAATTTTTGTATG | 317 |
rs569346478 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688368 | GCTCTAGTTCAGGCT[A/G]TTGTCTGCTCATGCC | 317 |
rs569396885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726109 | TGCTAGGCCAGTTTT[C/T]ATTACCCTGCAGTGC | 317 |
rs569415647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684210 | GTACTGAAACAGTTA[C/T]TGAAAATTGCCGTCT | 317 |
rs569469304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702300 | TCGATCTCCTGACCT[C/T]GTGATCCACCTGCCT | 317 |
rs569512005 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645647 | GCCCCGGGGCTGCAG[A/G]GATCCAGGGGAGGCG | 317 |
rs569534831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695229 | GGCTCATTTTTGTGT[C/T]TTTAGTAGAGACGGG | 317 |
rs569558395 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98680909 | ACAAACTTGGGGATT[A/C]CTGTTGTAAGATACA | 317 |
rs569586796 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698979 | CTGCTAGGTCACGAC[C/G]TAACTTGGACTGGGT | 317 |
rs569615516 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98722260 | TCTCTAAGGAATTAC[-/T]TTTTTTTGAGTTTCA | 317 |
rs569666509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680046 | AATCAACACCCCAAA[G/T]ATCCTGTAACATTTT | 317 |
rs569678616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673005 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 317 |
rs569775890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718301 | GCAGTGGTGCAATCT[C/T]GGCTCACTGAAACCT | 317 |
rs570037661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689578 | GATCCTCCTGCCTCA[A/G]CCGCCTGAGTAGCTG | 317 |
rs570058825 | snp | C/G/T | 5.68794e-05 | 0.00533264 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735516 | AGCTAAATACATCAA[C/G/T]CTTTCTATTTAGGCT | 317 |
rs570101496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682001 | TGTTGTTATATGGCA[C/T]AGACTGCTTAGTTGT | 317 |
rs570108643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718772 | AGACCCCATCTCTGC[A/G]AAACAAAATAATTTA | 317 |
rs570134342 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734584 | GAGGGTAAGGGAATA[C/G]ATCACTCAGATGTAT | 317 |
rs570155240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646986 | TAGTAACAATGCTCT[A/G]TTCACTCTTATGTTT | 317 |
rs570192339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647804 | TGGCTGCATAATATT[A/C]CATTTTATATACATA | 317 |
rs570250043 | snp | A/G | 8.28494e-05 | 0.00643567 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665774 | ATCCTTCAGAAGGAC[A/G]TTAAGGTGCCTACAA | 317 |
rs570275439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98651598 | AGCTGGGTTGAACTT[C/T]TATGTGAGTAAGAAT | 317 |
rs570280673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98703179 | CTTTATAGAAAATAT[A/G]TTTTAAGATGAGCAG | 317 |
rs570363184 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656205 | AGTGCTGGGAGCCAC[C/T]GTGCCAGGCTCTAAA | 317 |
rs570420790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700268 | CCAAATGATTTGTCT[A/T]AAGTTACATTGTGAT | 317 |
rs570433331 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98655846 | TGGAGTGCAGTGGCG[C/T]GGTCTCGGCTCACTG | 317 |
rs570483617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98700874 | CGGTCCTTTTGTGTC[A/T]GACTCATTTCATTGA | 317 |
rs570521793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98714375 | CATATGGTGTAGCCT[C/G]ATATCATCAAATAAT | 317 |
rs570592903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98708728 | TTTTTAGAAAACAAT[C/T]GGAAAATTGTTTTGG | 317 |
rs570593955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98722663 | CCACATGAAAAACAA[C/T]GCCTTCTCACTTCCG | 317 |
rs570655834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701762 | GTGTTCCTTAACTGC[A/G]TGTAGATCCCGATTT | 317 |
rs570669591 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98670068 | TTCCACCTCAGCCTC[C/T]TGAGTAGCTGGGAGC | 317 |
rs570680739 | in-del | -/TGT | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98710842 | CAACTAGTTCTATGA[-/TGT]TGAATAAATTGTATC | 317 |
rs570685568 | snp | A/G | 3.33239e-05 | 0.00408177 | intron-variant | APAF1 | GRCh38.p7 | 12:98662451 | ATATTTTTTTTTTAA[A/G]TTAGGTCTCTCTTGA | 317 |
rs570741124 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant | APAF1 | GRCh38.p7 | 12:98706468 | GTGATTTCCTATATG[C/T]TGTGTTTATTCTGTA | 317 |
rs570783028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98671171 | TTAATGATGGGAATG[A/G]GCAGAATAGAAGGGG | 317 |
rs570870557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664037 | TATTTTATTTATTTT[C/T]TGAGACGAGTCTCAC | 317 |
rs570883168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98656941 | TTGACGATTGGAGTT[C/T]GTAGATTATAACCTT | 317 |
rs570907987 | snp | C/T | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665374 | CTGAATGAAATCTTT[C/T]TTATTTCTAATTTTT | 317 |
rs570961178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98648986 | TTGCATCCACATTAA[C/G]TCTCAACTTTTCTTC | 317 |
rs570983494 | in-del | -/GGGT | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98668577 | AGCATGGAAGGGGAA[-/GGGT]AGAAAGTGATGATAG | 317 |
rs571007553 | in-del | -/TTAA | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732659 | CTTTTTATAAAGCTC[-/TTAA]TTGTTGTGCAGTATT | 317 |
rs571018129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98686048 | TTATCATACCATACT[A/T]TTATCACACCTAACA | 317 |
rs571077410 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723068 | CTTCTCTCTTATTCC[A/T]CTCTGTTTTACTGAA | 317 |
rs571100868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715887 | TTTCTTTACAGTAGT[A/G]AAATCCAATGGAAAT | 317 |
rs571108475 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669436 | ACCATTACTAATGCT[C/T]TTGTGTATAGTTTTC | 317 |
rs571143936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732219 | TTGGGTGTAGGCGGA[A/G]CAGTGAGGCCATCAC | 317 |
rs571205132 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98654797 | TTGTTTGTTTAAATA[-/T]TTTTTAAAGTAGTAT | 317 |
rs571207339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666639 | CTTGTCATTTTTTTC[C/T]GTCTCCTCAAATCTG | 317 |
rs571316387 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735480 | TTATCTGTTGATTAG[A/C]CCACTAAAGTGAAGG | 317 |
rs571338971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661099 | GTAGAGATGAGGTTT[A/C]ACCGTGTTAACCAGG | 317 |
rs571398131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98729363 | TGTTCCACCTCAGAT[C/G]ATCAGCATTAGATTC | 317 |
rs571504783 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98647918 | CTTTTTATTTTTTAC[C/T]CTAGCCTCCCAATGT | 317 |
rs571512868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726965 | CTTTTTCTTATTCTG[A/G]TGTACCTTTATTTGA | 317 |
rs571521427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718999 | CCTCTCAGTTATTTC[A/G]ACCTTCTCTTTCCTT | 317 |
rs571576581 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98727546 | AGCGACATCCTGTCT[-/C]AAAAAAAAAAAAAAA | 317 |
rs571613993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692171 | CACTGCAAGCTCCGC[C/T]TCCTGGGTTCATGCC | 317 |
rs571665161 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693446 | TTCAGGGTTTACATC[A/G]TTGTAACTAATCACA | 317 |
rs571680313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684106 | TGATATTTTTGAGAG[G/T]GGTAGTAAAAGACAT | 317 |
rs571739195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98677292 | TCATTTGCATGTTAG[C/T]AATCTGATTTTAAGA | 317 |
rs571827465 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695452 | TCACTGCAGCCTCAA[C/T]CTCCTAGGCTCAAGT | 317 |
rs571901754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653261 | AAAACCTTTTCTTTT[A/G]AAAGTACAGATAATA | 317 |
rs571997444 | in-del | -/AA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677911 | AATACCTATTTTATC[-/AA]AGTCTTAGGCATAGG | 317 |
rs572035827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723870 | GCTCTCTACATGTCT[G/T]TTTCATATTTTGTGA | 317 |
rs572065894 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98687286 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 317 |
rs572168034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98693180 | ATTTTATTTTTTTGT[A/G]TGTGGCTACTGTAAA | 317 |
rs572179845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98708283 | GTATCAAACAGTTTG[A/T]TAACCAGCAGGAGGT | 317 |
rs572250433 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721249 | AGCTGCAAAGGCTAT[G/T]CTTAATCTGCCCTCA | 317 |
rs572268949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98723123 | GACAAGAGAATGTAC[A/G]CTCTCTCCACCCCTC | 317 |
rs572288228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656684 | ACTTCTTAGAATATT[C/T]GCCGTCTTGCCTTAT | 317 |
rs572293113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98685695 | GGCTGGAGTGCAGTG[C/G]AGCGATCTTGGCTCA | 317 |
rs572336784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718159 | TTCTAGTTTGCTGTC[A/G]CTGTCTGTCTACTTT | 317 |
rs572404826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98686361 | ACCATTTTTAGGGTT[A/G]GATAACCTGACATTT | 317 |
rs572412376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98650040 | CACTGACCTTAGCGA[A/T]CCTGGTAGGTTCTCA | 317 |
rs572452537 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98678853 | CGCCTCGGCCCCCTC[C/T]GGACTTTGGGTGCTG | 317 |
rs572466450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690710 | GGTCTGTTCATCCCT[A/T]ATTTATTTGCTTTTC | 317 |
rs572479625 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729062 | CAATAAAGTCCCTAA[A/G]GTTTAGAAGGGGTCT | 317 |
rs572495875 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732160 | TCCTGTCTGCAGCTC[C/T]CAAGCAGGCTGCATG | 317 |
rs572529229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682900 | AAATGTCATGTGTTC[A/G]TGACACTCTAGTTAT | 317 |
rs572530010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664257 | CTCCTGACCTCGTGA[C/T]CCACCTGCCTCAGCC | 317 |
rs572588413 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733815 | TTCTCACTGTAGCTG[C/G]TGGCAGCCCTGTGCC | 317 |
rs572697485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98702355 | CAGGCGTGAGCCACC[A/G]TGCCTGGGCTACTAA | 317 |
rs572838888 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735811 | GGCAGAAAAAGTAAA[C/T]AAGTAAAATCTATAG | 317 |
rs572842999 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645310 | CGGAGAAGAAGAGGT[A/G]GCGAGTGGACGTGAC | 317 |
rs572865403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98715271 | ATATATATATATATA[C/T]ATATATATATGACAT | 317 |
rs572947558 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650304 | CCTGGGCAACATGGT[A/G]AAATCCCGTCTCTAC | 317 |
rs572974164 | snp | G/T | 1.6477e-05 | 0.00287024 | intron-variant | APAF1 | GRCh38.p7 | 12:98667503 | TCTGAAACGTTTCAT[G/T]GGGTTGCAGGATCTA | 317 |
rs572974450 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711395 | GAATAAAACATTTTT[A/T]AGTTACTACTTAAAG | 317 |
rs572987240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707541 | TTCCAACACTCCACT[A/G]CTTCTCTGGCTCATT | 317 |
rs572989063 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676707 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 317 |
rs573008287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652687 | GCTGGAGTGCCATGG[C/T]GCGATCTTGGCTCAC | 317 |
rs573025851 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653084 | CAAGTAGTCCTATTA[C/T]AGTCTTATTATTCAT | 317 |
rs573063285 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644918 | CCTAGGAGAGGTGGG[C/T]GGCGACCTCAACCCA | 317 |
rs573140220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705542 | GAGGTACTTGTTTTG[C/T]CCATGCTAGTTCTGA | 317 |
rs573189029 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98656739 | TTACTACCTTCTCCA[-/T]AACCTTCTTAAGTGA | 317 |
rs573192180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713798 | ATTTTCATAAGGAAT[C/T]ACACAAATATTCTCT | 317 |
rs573202813 | snp | A/G | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659226 | CTGGGCTTCTGATGA[A/G]ACTGCAGAATCTTTG | 317 |
rs573241860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98699905 | AAATGTATTTAAAAC[A/G]TAGAATGCTTTCTTC | 317 |
rs573254870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662233 | TATGTTCTGATTTAG[A/G]GTTTGAGGAGAAGGC | 317 |
rs573318327 | snp | G/T | 3.38851e-05 | 0.00411599 | intron-variant | APAF1 | GRCh38.p7 | 12:98662656 | ATTACTTACTTTGTC[G/T]TGTGATTTTTGTTTG | 317 |
rs573318416 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98654725 | TTTTACAAATTTTAG[G/T]TAGTACAAATTTAAA | 317 |
rs573328920 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | APAF1 | GRCh38.p7 | 12:98656034 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 317 |
rs573334153 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98700458 | ATTGATTTAGTGCTA[C/G]AATCCTTGGATGTTG | 317 |
rs573387679 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677497 | TGTTTACCATGCCTG[C/T]TTTTCTGAGGATGGT | 317 |
rs573410139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729561 | CCACAGACCAGTACC[A/G]GTCCATGGCCCAGGG | 317 |
rs573419861 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708478 | TCTAATATTGAAACC[C/T]TTCTAGCATCATAGG | 317 |
rs573431988 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681819 | TGTTTTCTAAGCCAG[A/T]GGTAGAAATACCTAT | 317 |
rs573450623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669584 | CATGTCATTTATATA[C/G]AGTGACATGATTTTT | 317 |
rs573544665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710017 | AGTAGCTGGGACTAC[A/G]TGTGTGCTACCACGC | 317 |
rs573548152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661387 | GCTTACAAAGCCAGG[C/T]ATATTTTTTTAATCT | 317 |
rs573599549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98717803 | AGCTCTCAGTGGTCA[C/T]TGGCTATCAGAGATC | 317 |
rs573630569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710729 | ATGCCCCACTCAAAC[C/G]TTAACAAGTTGTAAA | 317 |
rs573659135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705326 | AGATGGGGAGAAGAA[A/G]GTGGGAAGAGAGGGG | 317 |
rs573667915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702494 | ATTTGGCAAAAACTT[C/T]GGAAGAGTATATTCA | 317 |
rs573669247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98651065 | AATTGTTATCTTGGA[A/G]CAGGTTTTAACTACT | 317 |
rs573713801 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651457 | ACACAATGTTTTTAA[G/T]ATTTATCCTTGTTGC | 317 |
rs573732089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658950 | CACAGATTTACTTCA[A/G]ACTTCAGTTTCTTCA | 317 |
rs573772167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679726 | GTTCCCCGGTGCCAG[A/C]GTGTAAGCTGCTTGT | 317 |
rs573780976 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733321 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 317 |
rs573787578 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677948 | TTCTTGTAAATAGGA[A/G]CTGGACTAGACTATT | 317 |
rs573821603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98673188 | AATGGGATTTAAACC[C/T]TGGATCTTGTGGCTG | 317 |
rs573843831 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668713 | GAAAGAACGGAGTCC[A/C]TGAACTGAAACAGGG | 317 |
rs573847110 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696891 | TAAACCCTGAAAAAG[-/A]AAAAAAGTATACTTC | 317 |
rs573969764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674192 | AGATAAGGTCTCACT[A/G]TGTTGCCCAAGCTGA | 317 |
rs573976579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727376 | CATACTTTCCAAGCT[A/G]TTTTCACTTCCTGTT | 317 |
rs573989624 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703040 | GAGTATTCATTTTCT[C/G]TTTTGAATAAACAAG | 317 |
rs574158174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670455 | TACTGTTTTATTAGA[A/T]TTTTCTATAAAAAAT | 317 |
rs574172271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719243 | TCCTAATTCTTAATA[C/G]TTATATTCTTAGCCC | 317 |
rs574225129 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734045 | TTTTCTAAGAAATGT[A/G]AAATAGAACAATTTT | 317 |
rs574265054 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734940 | TAAAAAGCCTTGAAT[A/G]GCCCTTGTCTTAAAA | 317 |
rs574290170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726453 | GATCTAAAACTCCAG[C/G]AACAGGTATATAGTG | 317 |
rs574344514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98677774 | GGAAGTGCCCTTTAC[C/T]CTGCCAGTCAGTTCC | 317 |
rs574362806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98685492 | AGGTGCCGTGCCACC[A/G]TGCCTGGCTAATTTT | 317 |
rs574401264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731002 | AGTATGGAATACATG[A/G]TGATAAATGGTGGTG | 317 |
rs574413991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689827 | AGTACATATATCTAT[C/G]TATATCTATAGGTAG | 317 |
rs574441160 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692878 | GTCTTTTTGGTAGAA[A/T]GATTTGTTTTCCTTT | 317 |
rs574507281 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694901 | TTTTTTTTTTAGACA[G/T]TCTTGGTGTGTTGCC | 317 |
rs574668493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98671264 | GGAAAGTAGGTAGGA[C/T]TGAAGTTTAAAAGCT | 317 |
rs574668665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662913 | ATGAACATCCAAAAA[C/T]TTTTCTGGGAGATTT | 317 |
rs574694082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701926 | TTGCCAAGTTTCCTC[A/G]ATCACTGTCAGCCAC | 317 |
rs574697776 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98692490 | TGATGCCGAGGTTTG[G/T]GTACAACTGGTCCTG | 317 |
rs574731357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663639 | TTGTTATGCTTGGAA[A/G]TACCTTATTTTTCTT | 317 |
rs574787735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98649151 | TTAGAAATATATGTT[A/C]TTGAAAGGTATTCCA | 317 |
rs574812028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98693053 | CCTCCCTGGCATCTT[C/T]TATTTTTTGACTAAA | 317 |
rs574842868 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720988 | AAAGAAAAAAAAAAT[G/T]TCCTTAACATTTCTA | 317 |
rs574847982 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98697468 | TTAAAGATGATAAAC[C/G]CTTGCTGTGTCACTT | 317 |
rs574890369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663225 | CTTGTTTATTGAATA[C/T]GTTTTAAGAAGTTAT | 317 |
rs574891254 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732870 | TTCAAAATGGTTGAC[A/G]TAATTAATGAGAAGA | 317 |
rs574909445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698395 | TTTCTCATATATTCT[A/G]GATAATGTAACTGAA | 317 |
rs575025748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98690636 | AAAACTAGGCCATTT[A/G]TGTGTTGTACAAATA | 317 |
rs575073263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666079 | TTAAGAAATGGAGAC[A/G]TTCTTACTCAGGGCT | 317 |
rs575135198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98666803 | GCAAGAATACCAATG[A/T]TGTTGTATCTTTCTC | 317 |
rs575158183 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651236 | ACTAGGCTGAGCTTT[C/T]CACTGTATTTATTTA | 317 |
rs575202612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98697598 | AATGTGATTGTGGCT[C/T]ACAGAGCACTCGCAG | 317 |
rs575241845 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683953 | TTGATTGTATCTTTT[C/T]TTCCTCTTAAGTGGA | 317 |
rs575244568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98728855 | CTAGTGATTGAGGCC[A/G]CAATTTGAATGTGTT | 317 |
rs575337806 | snp | G/T | 4.86251e-05 | 0.00493054 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644530 | CCACTTACCAGGCCA[G/T]GCCCAGGCACGTCCC | 317 |
rs575347848 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674746 | TAATGGTAGTATTTT[A/G]TAGCATTGTTGTGAG | 317 |
rs575373606 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644824 | CACAGACTTGGCACC[A/G]CCCAGAGCCCAGCCC | 317 |
rs575399468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659838 | TTTAAAACGAAAAAA[A/G]AAAGTGGCTGCCACT | 317 |
rs575433966 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98712064 | TCAGGTGGCGGGCGC[A/C]GCAGCTGCTTTTTAA | 317 |
rs575434651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98659070 | GTGATGGGATTGTAA[A/G]TTGGAGTAAATCTGA | 317 |
rs575463501 | snp | C/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644310 | TCTGAGCGATAGGGG[C/T]ATGCTACCAGCACGG | 317 |
rs575483878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719051 | ACTCCATTGGATTCT[A/G]TTCCCTGTGGTTTCT | 317 |
rs575510790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679673 | CCTCTTTGGGGCCCC[A/G]CGGTTCCTGGCATCT | 317 |
rs575533380 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | APAF1 | GRCh38.p7 | 12:98720588 | TTGGTAGTTTTTGAT[A/C]CTTTACCTTGAAGTA | 317 |
rs575545663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98721111 | CTTTTGCATTTGACT[A/G]ATGGTGGTGGAAGTT | 317 |
rs575546305 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653343 | TGGGTGGTGATTGGC[A/G]TAAATTAAAGAATAT | 317 |
rs575626989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705809 | TTAGTGGAAAATAAT[A/C]TGAATATGGAAGCTG | 317 |
rs575642787 | in-del | -/T | 0.469148 | 0.120308 | intron-variant | APAF1 | GRCh38.p7 | 12:98662148 | GATAGTAATGGTCGC[-/T]TTTTTTTTTTTTTTT | 317 |
rs575662140 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656298 | ATTCTCTGCAATTAT[A/G]AATATATACACATAC | 317 |
rs575707221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98654617 | TTCACCATGTTGGCC[A/G]GGTTGGTTTCGAACA | 317 |
rs575715490 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695110 | CAGGCTGGAGTGCAG[G/T]GGCGTGATCTCAGCT | 317 |
rs575741771 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656581 | TACATTGCCAAATTC[C/T]GATCTAAGTCTTCTT | 317 |
rs575746787 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98661323 | TGCAAAATTAAAATT[C/G]ACTTCTGTTGAGTAA | 317 |
rs575800230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683399 | GAAACTACAATAATA[C/T]ATTAGCTGAAGCAAA | 317 |
rs575848340 | snp | C/T | 1.94015e-05 | 0.00311454 | intron-variant | APAF1 | GRCh38.p7 | 12:98699393 | CTTTTTCTTTTTTAT[C/T]ACTTTAATTCAAAGC | 317 |
rs575870498 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709083 | AGGATTCCAGGGTCT[A/T]TGAAAGAACAGAAGT | 317 |
rs575882277 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681497 | ATATGGAAGACAGAC[C/T]TTACTTTAACCCTTT | 317 |
rs575911531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675943 | TTATGTGTCGGGTGC[C/T]GTTTAGAATAGATAC | 317 |
rs575996323 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732938 | TATTACTGTTATGCA[A/G]GCTGTGCCTCAGGGT | 317 |
rs576033687 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710871 | TATCACGTCTTTGAG[C/T]CTCAGTTTGTAAAGG | 317 |
rs576034246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729837 | AAAGATAAATTAGAG[A/G]ACAGTTTTTAGCTTT | 317 |
rs576062205 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98657414 | GGAAGTGGAATAGGT[A/G]TTTGCTCCTCAAGGC | 317 |
rs576079253 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645830 | GACCTAGGCGCAAAG[C/G]CTTGGGTAAGTTGAC | 317 |
rs576083748 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700314 | TTCTGATTTATGGCT[C/T]ACTTACATTCTCATC | 317 |
rs576101911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709892 | TTTCTTTTGTTTTTC[C/T]TTTGAGACAGTTTCT | 317 |
rs576105401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98672456 | AGGCATGAGCCACCA[C/T]GCCTGGCCTTCTGTG | 317 |
rs576153636 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721454 | GTGAAGCCCAGAAAG[C/T]GGGAGGAGAGAGCCA | 317 |
rs576179485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98687192 | AGATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 317 |
rs576287580 | snp | A/G | 4.95692e-05 | 0.00497816 | intron-variant | APAF1 | GRCh38.p7 | 12:98725364 | GCAATCAAGGCAGAT[A/G]CTTATTTTGAGTGTT | 317 |
rs576318298 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647379 | TGATACCAACACTTG[-/T]TTTTTTTTTTTGAGA | 317 |
rs576331303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | IKBIP, APAF1 | GRCh38.p7 | 12:98643241 | CAGGTGTGAGCCACC[A/G]CGCCCAGCCGTAACA | 317 |
rs576362691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681135 | GGTACAATCTCGGCT[C/G]ACTGCAATCTCTGCC | 317 |
rs576369294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98671749 | AGAGAAACCAAAGGG[A/C]GTGGTGCGCTAACTA | 317 |
rs576436585 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700929 | TTGTAGCATGTATCA[A/G]AACTGTATTTCTTCT | 317 |
rs576439382 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98679695 | CTGGCATCTCCAAGC[G/T]TCTGGGCACCACCGT | 317 |
rs576561234 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661520 | TCGCTCTTGTTGCCC[A/G]GGTTGGAGTGCAATG | 317 |
rs576612967 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98652878 | TGATCCCCCTGCCTC[A/G]CCTCCCAAAGTGCTG | 317 |
rs576621437 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | APAF1 | GRCh38.p7 | 12:98727125 | GTTTTAAAACCAGAG[A/G]AGCTTCTGGATAACT | 317 |
rs576673127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98653485 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 317 |
rs576691742 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645378 | GGGAGTCTGGGCAGT[A/C]GGCGACCCGCGAAGA | 317 |
rs576703546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688194 | TCTTCCTCAAATCCC[C/T]ACCTTCTCCAATAAG | 317 |
rs576781746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98700632 | GCATATAATGTAAAA[A/G]TTGCCATTTTAACCA | 317 |
rs576793308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684344 | TCTGGCTGAATGGGA[A/C]CTACATTTCTTCTTG | 317 |
rs576838832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696383 | GAACTAATCCATTCC[C/T]AGGGAACTCACCCCA | 317 |
rs576861432 | in-del | -/AC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717353 | ATATAGAAATTATAT[-/AC]ACACACACACACACA | 317 |
rs576900336 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714353 | TTTACCTATAAAGTG[A/G]CAGTTTCATATGGTG | 317 |
rs577019185 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693259 | CAGAAATGCTGCTGA[-/T]TTTTTTTTTTCTTAA | 317 |
rs577021225 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98678386 | CTGTGGAGCTGGCGG[G/T]AGCTGGGGACAAGCA | 317 |
rs577021602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730690 | TGCATCTACCCAGCA[G/T]GTTAATGAGACTATC | 317 |
rs577154639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656075 | GGCATGAGCCACCGC[A/G]CCCGGCCTTGCCTGG | 317 |
rs577184220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98693489 | CGTGTGAATTTTTTT[C/T]CTCTCTCATTAGCTT | 317 |
rs577187794 | snp | A/T | 4.94262e-05 | 0.00497098 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703446 | ATCCAGTACTGTGAC[A/T]TCTCCCCACAAAACC | 317 |
rs577326997 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689766 | CCTGGACTGCAAAGC[A/G]TTCTTCAGAAAGTGT | 317 |
rs577337025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98647346 | TGAATAAACTTCTAA[A/G]CGTCTATATATATTC | 317 |
rs577377731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98648213 | AAATTTTTGCCAAGG[A/C]AAAAAAATCAGTTTT | 317 |
rs577380501 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98658836 | TTGCCATCCCAAAAA[-/G]TCAGAAGTACAAGGT | 317 |
rs577448072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98715333 | GATGGAAATTCTGTA[A/C]CCTCCAGTCTAATTT | 317 |
rs577464937 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656779 | TTTTTTCCTTTATAT[-/C]CTACATACTTTAGCA | 317 |
rs577476998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98705213 | TTACCCTCTGCCATC[C/T]TTAGCAATCTCCAGG | 317 |
rs577521294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98710843 | AACTAGTTCTATGAT[A/G]TTGAATAAATTGTAT | 317 |
rs577576897 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98678411 | CAAGCAGGAACCCTA[C/T]CCCTTCTGAATTGGG | 317 |
rs577610969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659677 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 317 |
rs577633487 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643662 | TTAAGTGAACACAAG[C/T]GCTATGTTTTTGTAG | 317 |
rs577635656 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98659985 | AAGTGCAAACTTCTT[A/C]CTTTGAATCCGTTAT | 317 |
rs577637788 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726853 | CTACCTTACTGAACT[A/G]TTTCTAATGAGTTTT | 317 |
rs577649499 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98696581 | TGTGTTCTCTGCATC[G/T]TTAACACCTGAACCC | 317 |
rs577710208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98697426 | TATATAGTCTCAAAG[G/T]GACTAGCATAGTGTT | 317 |
rs577757125 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645925 | ATTTGAGGACATGGA[A/G]TATTTGATAACCATC | 317 |
rs577768952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674029 | TGAGACAGGACCTCA[C/G]TTTGTCATTTAGGTT | 317 |
rs577777193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665381 | AAATCTTTCTTATTT[C/T]TAATTTTTTTTGGGA | 317 |
rs577791032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726280 | TATGGAAAGAATTGC[A/G]TGCTGAAAGATTAGA | 317 |
rs577829543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98665900 | TAAGACCCAGGGGAC[A/T]GAGGTGGTGGGGTGT | 317 |
rs577850295 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734997 | ACGTGCCTGTAATCC[C/T]AGCTCCTTGGGAGGC | 317 |
rs577914203 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735674 | TTATTCACTTAGTTT[A/G]TTCATGCATTTGTTT | 317 |
rs577927833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98720357 | TAACAAAACTCTATA[C/G]ATATTTTCGAGAAAT | 317 |
rs578012799 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678339 | GCCATCATGCTGGCT[A/G]CAGCAGGGAGGCGCA | 317 |
rs578020483 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98713037 | TTGCCCAGGCTGGCC[G/T]TAAACTCTTGGGCTC | 317 |
rs578044186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98721018 | ACAATTTAAATTTTA[C/T]TCATATAGCTGAAAA | 317 |
rs578053697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98713447 | GTGCAGGGCTGCCTG[C/T]GCTTGCCTGTTCCAC | 317 |
rs578069495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675761 | GTCCTAGAACCAATC[A/C]CTCATCAATACTGAG | 317 |
rs578078931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689876 | TCTGATTTCCACTTA[C/T]AAATGTGTTGTACTG | 317 |
rs578174920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98705125 | AAGTAAATGTGGAGC[A/G]TTTGTTAGGATTTTT | 317 |
rs578193557 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708724 | GTATTTTTTAGAAAA[C/T]AATTGGAAAATTGTT | 317 |
rs578193753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98727581 | TGGCAGTAAAATGAG[A/T]TTAGTAACTAAAGAA | 317 |
rs578212318 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706432 | TTCAATATTTTTGCT[C/G]TCTTCAAAATGCTTA | 317 |
rs578257927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98682760 | ATTTGTGACACACAA[A/G]TCATAAGTGGTAGAG | 317 |
rs578259044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675194 | TATAGAAAGGTTTAG[A/G]TTGGTATAAGCTTAA | 317 |
rs745324859 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656056 | CAAAGTGCTGGGATT[-/A]ACAGGCATGAGCCAC | 317 |
rs745331570 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681124 | TGGAGTGCAGTGGTA[C/G]AATCTCGGCTCACTG | 317 |
rs745348129 | snp | G/T | 1.79268e-05 | 0.00299384 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644657 | GGGCTCCGCAGCAGG[G/T]GCTCCCTTGGGCCCC | 317 |
rs745352763 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690555 | AATTCCAAATTCTGG[A/G]AAGACTGCATTATCC | 317 |
rs745381849 | snp | C/T | 3.33433e-05 | 0.00408296 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732382 | TGTCACACAGTGTAA[C/T]TACCAATCTAATGAG | 317 |
rs745395636 | in-del | -/ATT | 1.66316e-05 | 0.00288367 | intron-variant | APAF1 | GRCh38.p7 | 12:98648592 | GTTGCATACATATTC[-/ATT]GTTGTATACTAAACT | 317 |
rs745404599 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671691 | GCCAAGCAGGAGGTC[A/G]ATAATGGAATGCTTT | 317 |
rs745407782 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692438 | TAGATTCAGGGGTAC[A/G]TGTGCAGGTTTGTTA | 317 |
rs745436384 | snp | G/T | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648376 | TGGATGCAAAAGCTC[G/T]AAATTGTTTGCTTCA | 317 |
rs745453320 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715926 | TCTTTCCTTTTAAGA[A/G]CAAAATGTTTATTAC | 317 |
rs745482953 | in-del | -/T/TT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665538 | AGCATAGTGACTTCA[-/T/TT]TTTTTTTTTTAAAGG | 317 |
rs745529226 | snp | A/C | 0.000149744 | 0.00865157 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732496 | AGAAAATACACGTGT[A/C]CCCTGACTTCAAAAC | 317 |
rs745533546 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731347 | AGTCCGTAATTAGGG[C/T]TTGTTCTTGGTGCTG | 317 |
rs745558849 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696136 | TGTTTTCTGAAACAT[A/T]ATACCTGAGACTGGG | 317 |
rs745560384 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698319 | TGGCTTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 317 |
rs745564176 | snp | A/T | 1.85955e-05 | 0.00304916 | intron-variant | APAF1 | GRCh38.p7 | 12:98715400 | GCTTAGTTTCTTCTT[A/T]ATTTTCTGTGTTTTT | 317 |
rs745628140 | snp | G/T | 1.68604e-05 | 0.00290343 | intron-variant | APAF1 | GRCh38.p7 | 12:98648869 | AATTGCTTTGGGTTT[G/T]TCTTATTGTAGATGT | 317 |
rs745631210 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656524 | AGTTCTCTGTCTCCA[A/G]TTGTTTGTTATATTT | 317 |
rs745657317 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657341 | TTCTTAGCACATACT[C/T]TTGACTCTTTAGTCC | 317 |
rs745663782 | in-del | -/TATCATGTTTATGTAAATATGGAATGTC | 1.65312e-05 | 0.00287495 | intron-variant | APAF1 | GRCh38.p7 | 12:98727156 | TGTTAATGAATTGTG[-/TATCATGTTTATGTAAATATGGAATGTC]TATCATGTTTATGTA | 317 |
rs745664662 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715508 | ATCCAGTTCACAGCC[A/G]ATGAGAAGACTCTTA | 317 |
rs745676629 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710159 | GATTATAGGTGTGAG[C/T]CACCGTGCCCGGCCT | 317 |
rs745686802 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | APAF1 | GRCh38.p7 | 12:98683309 | ATTAGGTAGATAAAT[C/T]TGATTCGTACATCAG | 317 |
rs745777559 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720647 | CATGAGCCAGTATAT[A/G]GGACTATGTTAGTTC | 317 |
rs745789162 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686401 | GGGGGTAATTTATAT[G/T]ACATATTACTTATTG | 317 |
rs745791119 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686836 | TTTCACCAGATGATA[A/T]GCTTTTGGCTAGTTG | 317 |
rs745840047 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722126 | AGGTCCCTTTTCACG[C/T]TTCCCTGCTCCTATA | 317 |
rs745844200 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672077 | AATTCTGTGACTTTG[A/G]ACAAGTTACAGGTTT | 317 |
rs745862330 | snp | C/T | 4.96964e-05 | 0.00498455 | intron-variant | APAF1 | GRCh38.p7 | 12:98667675 | TAAAAATTCTTTTAT[C/T]TGACTTCCCTTTTTC | 317 |
rs745869743 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699713 | CCTGTCATGGTTCTT[C/T]GGAACTGTGCTCCGT | 317 |
rs745902161 | snp | A/G | 3.32094e-05 | 0.00407475 | intron-variant | APAF1 | GRCh38.p7 | 12:98708544 | AGATGAAGACATGTT[A/G]TTTTAGAGATGGAAT | 317 |
rs745909861 | in-del | -/TTC | | | cds-indel, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662524 | ACAGTCAGTGTCAGA[-/TTC]TTCTTACAACCAGAG | 317 |
rs745910434 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647057 | TGTAATCACTATTTT[A/G]TACAATCTTAATTAA | 317 |
rs745914937 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682076 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTTT | 317 |
rs745929548 | snp | A/C | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648467 | TGATGGATTTTTAAC[A/C]ATATCAGAAGAGGAA | 317 |
rs745941566 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726986 | CTTTATTTGAAAAAT[A/T]AGAGCACTGCTTATA | 317 |
rs745954515 | snp | A/G | 1.66529e-05 | 0.00288551 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708671 | AGAAAATGAAGTGAT[A/G]GTCCTTGCAGTTGAC | 317 |
rs745962333 | snp | A/G | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648692 | GATAATGATTCCTAC[A/G]TATCATTCTACAATG | 317 |
rs745966963 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654546 | CCAAGTAGCTGGGAC[C/T]ACAGGTGTGTGCCAC | 317 |
rs746026740 | snp | A/G | 3.32497e-05 | 0.00407722 | intron-variant | APAF1 | GRCh38.p7 | 12:98648582 | ACTACTTTATGTTGC[A/G]TACATATTCATTGTT | 317 |
rs746066041 | in-del | -/AAATAAAG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720603 | CCTTTACCTTGAAGT[-/AAATAAAG]GCCAAGTATTACCCA | 317 |
rs746088959 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661180 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCT | 317 |
rs746117309 | in-del | -/G | 1.6941e-05 | 0.00291036 | intron-variant | APAF1 | GRCh38.p7 | 12:98723618 | TGTCAACCTCCAAGT[-/G]GTTTTTTTTTTTTTT | 317 |
rs746130435 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683163 | GAATTCTATGACTGG[A/G]GAACTAGTACACACC | 317 |
rs746141016 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662355 | TTTGTTTTAAAAAAA[A/G]TTTAATTTGGTAGAT | 317 |
rs746177196 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700993 | CACATTTTTTCTTTG[-/T]TTTTTTTTTTTCTTA | 317 |
rs746187312 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692593 | TTGTTCTTATCTTTA[C/T]GTCTTTGTGTACCCA | 317 |
rs746207393 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667827 | CTCAGGCTGGAGTGC[A/G]GTGGCACAATCTCAG | 317 |
rs746245652 | snp | A/G | 2.48019e-05 | 0.00352141 | intron-variant | APAF1 | GRCh38.p7 | 12:98649729 | GTAAGGTAGATAGAC[A/G]TGTAAAAATATTATG | 317 |
rs746246585 | snp | A/G | 0.000138911 | 0.00833283 | intron-variant | APAF1 | GRCh38.p7 | 12:98723636 | TTTTTTTTTTTTTTT[A/G]AGGTATGGAATATTA | 317 |
rs746268838 | snp | C/T | 1.65059e-05 | 0.00287275 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666348 | AGAGAAGAATTGCAG[C/T]CAGCTTCAGGTACTT | 317 |
rs746326392 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659193 | TGCATTGGGTTTCAG[C/T]TGGGAAACAAGACAA | 317 |
rs746354452 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704608 | GCTTCTCCTAATTCT[A/C]GGTGCAGCAGTGCAT | 317 |
rs746374886 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723749 | TTCATCTACCTCTGC[C/T]GACAAGACTGCAAAG | 317 |
rs746385368 | snp | A/G | 1.65023e-05 | 0.00287244 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699556 | TAATGGTGGCAGCAA[A/G]AAATAAAATCTTTGT | 317 |
rs746392893 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690703 | GAATTATGGTCTGTT[C/T]ATCCCTAATTTATTT | 317 |
rs746413382 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703380 | TGACAGCTTTTTGAC[A/G]TTCATACTAGTGGCC | 317 |
rs746426956 | snp | G/T | 1.64806e-05 | 0.00287054 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671569 | ATTTTCAGGAGTTTT[G/T]ATCTTTAAATGGACA | 317 |
rs746440518 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653999 | CCTCCTGTGAAAGTA[A/G]TGTGGAGTTTTCCCT | 317 |
rs746448736 | snp | C/T | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729509 | TGTTCACTCACCAGC[C/T]GCTCACCTTCTGCTC | 317 |
rs746458215 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678535 | GGTGTAGCTGTAGCC[A/G]CCCAAACCACAGCTG | 317 |
rs746482334 | snp | A/G | 1.67276e-05 | 0.00289197 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732507 | GTGTCCCCTGACTTC[A/G]AAACATATGTGACTG | 317 |
rs746490911 | in-del | -/A | 1.65102e-05 | 0.00287312 | frameshift-variant, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665694 | ATGAGGCTCTAGATG[-/A]AGCCATGTCTATAAG | 317 |
rs746496117 | in-del | -/TG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696108 | AGTTTGGAAATGGTC[-/TG]TGTCTGTTCTCTGTT | 317 |
rs746515411 | snp | G/T | 1.68405e-05 | 0.00290172 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715433 | GCTTTGAAGATTTTA[G/T]AACTTGTAAACAATA | 317 |
rs746536627 | in-del | -/C | 0.000280433 | 0.011838 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677437 | TAGAAACAAAAAAAA[-/C]ATCACGAATCTTTCC | 317 |
rs746537250 | snp | A/G | 3.75446e-05 | 0.00433254 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735528 | CAACCTTTCTATTTA[A/G]GCTTTATCAGCTATA | 317 |
rs746547221 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667396 | GCTGGGATTACAGGC[A/G]TGAGCCACCGAGCCC | 317 |
rs746549280 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695504 | TGAGGAGCTGGGACT[A/G]CAGGTGTGCACCACC | 317 |
rs746604749 | snp | A/C | 3.41448e-05 | 0.00413174 | intron-variant | APAF1 | GRCh38.p7 | 12:98648881 | TTTGTCTTATTGTAG[A/C]TGTAATCTTTTGAAG | 317 |
rs746614623 | snp | C/T | 0.000282761 | 0.011887 | intron-variant | APAF1 | GRCh38.p7 | 12:98665812 | GGGATCAATGATCCT[C/T]ATCATTGGGTATTTA | 317 |
rs746668454 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693019 | CCAGCAGTGTATAAG[C/T]GTTCCCTTTTCTCTG | 317 |
rs746699746 | in-del | -/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647027 | CAAGAAGTCTCTTAA[-/T]TATTAGGACTTCAAT | 317 |
rs746728734 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686863 | GTTGTTCAGCTGATG[C/G]AACCTTAAAGGTATG | 317 |
rs746732100 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686163 | GAATCAGAATCCAAA[C/G]AAACTTTATGTAGCA | 317 |
rs746738305 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712594 | CGATCACAGCCGACT[G/T]CAGCCTTGACCTTCT | 317 |
rs746765668 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669562 | TTACATTGAATGGTC[A/G]TCTTTTCATGTCATT | 317 |
rs746778861 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646584 | CTTCTTTGAGTAGAC[-/TG]TGAATTATTTCAGGC | 317 |
rs746781136 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671821 | GATTTAACTACTTTC[A/G]AAAGGGCTGGAACTT | 317 |
rs746811712 | snp | A/G | 1.66674e-05 | 0.00288676 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699420 | AAGCTTTGGGATGCG[A/G]CATCAGCAAATGAGA | 317 |
rs746812450 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682310 | TGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 317 |
rs746875464 | snp | A/T | 9.88794e-05 | 0.00703064 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662517 | GCTTTTGACAGTCAG[A/T]GTCAGATTCTTCTTA | 317 |
rs746876526 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720454 | TTATCTTTGTATCCC[C/T]AAAGCCTGGAATCCA | 317 |
rs746887648 | snp | A/G | 1.6513e-05 | 0.00287336 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671064 | ATGAATTTGTGGAAT[A/G]CAGACATATACTAGA | 317 |
rs746891424 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725567 | GCTGACATGAGAGCA[C/G]TGCTCTTCTTGTAGC | 317 |
rs746894632 | in-del | -/GCCCA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708104 | GGTGCACACCACCAT[-/GCCCA]GCCAAGTTTTGTATT | 317 |
rs746926896 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698628 | AGGTTTTACCTGGGA[G/T]TTGTGCTTTGGAAGC | 317 |
rs746933460 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707694 | TTATGCAAAGTACTA[-/TA]TATATATATATATAT | 317 |
rs746959740 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718666 | CCTTACTGGGCGCAG[C/T]GGCTCACACCTTTAA | 317 |
rs747009471 | in-del | -/A | 1.91881e-05 | 0.00309737 | intron-variant | APAF1 | GRCh38.p7 | 12:98648930 | TGAAAACTGCATGTT[-/A]AAAAAATTGTAGTGA | 317 |
rs747013535 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710632 | TCTCACTATGTTGAC[C/T]ACGCTGGTCTTGAAC | 317 |
rs747016494 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697382 | TGGCCTGTCAACTCA[C/T]TGAGGGTAGTATCTG | 317 |
rs747018045 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660726 | AGTACAAAGATAAAT[A/G]AAGCATTCCTTGGGA | 317 |
rs747055731 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730188 | CAAAATGTTGCATTA[A/G]CCTACATCTTTATTC | 317 |
rs747092806 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733484 | ATCACCCAGGCTGGA[A/G]TGCAGTGGCATAATC | 317 |
rs747108997 | in-del | -/G | 3.29998e-05 | 0.00406187 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732428 | GAACAGTGGTGGAAC[-/G]GTTGTCACTGGGGAA | 317 |
rs747204567 | snp | A/G | 1.65419e-05 | 0.00287588 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723659 | GAATATTATTACTGG[A/G]AATAAAGAAAAAGAC | 317 |
rs747210489 | in-del | -/AGGTATATATAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671085 | ATATACTAGATGAAA[-/AGGTATATATAT]TAACATGAAAAATTA | 317 |
rs747215847 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663176 | AAACTGGTGTCTTAA[-/T]TTGCATTTTTTTTTA | 317 |
rs747222525 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727614 | GAACAGAAAAAAATA[C/T]TGAAAACAAAAAAGA | 317 |
rs747226252 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725945 | GTGCTGAAAGAAAAG[A/G]TCTCTTTAGCACTAT | 317 |
rs747227563 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675558 | ACATGTACAGACTCT[G/T]TTCTTGTTATTATTT | 317 |
rs747251439 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659215 | ACAAGACAAATCTGG[A/G]CTTCTGATGAAACTG | 317 |
rs747259827 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709967 | TGCAACCTCCACCTC[C/T]TGGGTTCAAGAGATT | 317 |
rs747278919 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677116 | GTATCAAAGGAAAAT[A/G]GAAAGTGACATGTTG | 317 |
rs747297304 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | APAF1 | GRCh38.p7 | 12:98667505 | TGAAACGTTTCATTG[C/G]GTTGCAGGATCTACA | 317 |
rs747301528 | snp | A/G | 4.95364e-05 | 0.00497652 | intron-variant | APAF1 | GRCh38.p7 | 12:98659389 | AGGTCCCATGTCCCA[A/G]TAAGATGTAACTACT | 317 |
rs747306543 | snp | C/G | 2.38849e-05 | 0.0034557 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644588 | GGGGTCTGCCCAGCC[C/G]CCGCCTCCGCTGCTC | 317 |
rs747315377 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689302 | ATTTCAGCTACTGTC[C/T]CTGTATGTGTTTCTT | 317 |
rs747331633 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723759 | TCTGCTGACAAGACT[A/G]CAAAGGTAGGTCAAT | 317 |
rs747341698 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651939 | CCCACCTCAGCCTCC[A/G]GAGTAGCTGGGACCA | 317 |
rs747360468 | in-del | -/AA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727547 | GCGACATCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 317 |
rs747369160 | snp | C/T | 8.23906e-05 | 0.00641783 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659315 | GCTAAAGACCGTCTC[C/T]GCATTCTGATGCTTC | 317 |
rs747384651 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725422 | CCTTCCAGATCTGGA[A/G]TTTTGATCTCCTTTT | 317 |
rs747408213 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716928 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 317 |
rs747451623 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717339 | ATATATATAATATAT[A/G]TATAGAAATTATATA | 317 |
rs747502853 | snp | A/C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703146 | GCTAGCTTGAGAGCT[A/C/T]ATCTGTGATGAATTT | 317 |
rs747503376 | snp | C/G | 1.77751e-05 | 0.00298115 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644671 | GGGCTCCCTTGGGCC[C/G]CGACTTCTTCCGGCT | 317 |
rs747507106 | snp | G/T | 3.29489e-05 | 0.00405874 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703475 | CCATTTGGCAGTGGT[G/T]GCTTTGTCCCAGTAC | 317 |
rs747531870 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664541 | TTTTGGATTTTGCCC[-/T]TTTTTTTTTTAAAGA | 317 |
rs747537426 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671977 | CAGTACTAAGTGCTT[A/G]ACTTACTGTAATTTA | 317 |
rs747538511 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671714 | AATGCTTTACCTGGA[A/G]TGGATGTAAGTAGGT | 317 |
rs747572732 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650441 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 317 |
rs747618944 | snp | A/T | 1.64901e-05 | 0.00287137 | intron-variant | APAF1 | GRCh38.p7 | 12:98686919 | GTATTTTATGGAAAG[A/T]CTTATGATTTGATTA | 317 |
rs747624326 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705915 | TTTTATAATGCGTTA[C/T]ATTCAGAGAAGTCTT | 317 |
rs747669491 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656294 | CTTTATTCTCTGCAA[G/T]TATAAATATATACAC | 317 |
rs747749195 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683729 | CTAGGGTAACCCCAG[C/T]GGACAGTAGGATGGA | 317 |
rs747796064 | snp | A/G | 8.23852e-05 | 0.00641762 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667624 | CTGGCCTATCACATG[A/G]CCAGTGCCAAGATGC | 317 |
rs747818910 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667665 | ATGACCCATTTAAAA[A/G]TTCTTTTATCTGACT | 317 |
rs747821940 | snp | A/G | 1.65304e-05 | 0.00287488 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699444 | AATGAGAGGAAAAGC[A/G]TTAATGTGAAACAGT | 317 |
rs747823382 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705003 | TGGCCAGGGTGGTCT[C/T]GAATTCCTGACCTCA | 317 |
rs747836791 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699525 | TGTTGTTCGTGGTCT[C/G]CTGATGGTGCAAGGA | 317 |
rs747854765 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720139 | CATTGTATACTATGT[A/G]TTCTATCAAAAGTTA | 317 |
rs747875020 | snp | A/G | 1.65222e-05 | 0.00287417 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671068 | ATTTGTGGAATACAG[A/G]CATATACTAGATGAA | 317 |
rs747922133 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682520 | CTTGCTCAAGCTTAC[A/G]TTAAACTGGGAACAG | 317 |
rs747950449 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734310 | AGGGGAAAAAACTCA[A/G]TAACTAGCTATTTTT | 317 |
rs747973393 | in-del | -/A | 1.64836e-05 | 0.0028708 | intron-variant | APAF1 | GRCh38.p7 | 12:98666175 | GCATATTAAATACTT[-/A]ACAACAATTCCTAGG | 317 |
rs747979101 | snp | C/T | 1.69479e-05 | 0.00291095 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662802 | TATTATAAAAGAATG[C/T]AAAGGTATGGTTATT | 317 |
rs748042592 | snp | A/G | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644453 | CTCCGGCTGGATGTT[A/G]AGCCGGGTGGGAGCC | 317 |
rs748055027 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647429 | CCAGGCTGGAGTACA[-/G]TAGAGTGGTCTCGGC | 317 |
rs748071547 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709835 | CCCTGAGACATAGGA[C/T]TGAGAAGGACAGAAA | 317 |
rs748107954 | in-del | -/A | 0.000257739 | 0.0113491 | intron-variant | APAF1 | GRCh38.p7 | 12:98662438 | TCATTAGTGATTAAT[-/A]TTTTTTTTTTAAATT | 317 |
rs748116668 | snp | A/G | 1.6601e-05 | 0.00288101 | intron-variant | APAF1 | GRCh38.p7 | 12:98727342 | CCCAAGAACTGTGAA[A/G]GAAAATAATAGCCTA | 317 |
rs748132790 | in-del | -/TC | 1.95593e-05 | 0.00312718 | intron-variant | APAF1 | GRCh38.p7 | 12:98683127 | TATTTGTAAATTTTT[-/TC]TCTTTTCTCTTTAGA | 317 |
rs748135543 | snp | A/G | 6.84955e-05 | 0.00585176 | intron-variant | APAF1 | GRCh38.p7 | 12:98680426 | ATCTTTTCCTCTTGA[A/G]TTGTAATCACAACAG | 317 |
rs748153375 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697273 | GCCCTCAGCTTGAAT[A/G]TAGCCTCCCCACTGT | 317 |
rs748163554 | snp | C/T | 6.64673e-05 | 0.00576448 | intron-variant | APAF1 | GRCh38.p7 | 12:98648601 | ATATTCATTGTTGTA[C/T]ACTAAACTACTTAAT | 317 |
rs748179136 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659179 | TTTCCCAGGGGGAGT[A/G]CATTGGGTTTCAGTT | 317 |
rs748182585 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703322 | ATATTAGAATAGCTT[A/G]TCTCTTAAAGTATTT | 317 |
rs748239831 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706239 | ATGATATTCCATTAT[A/G]TGATTAATGTAGTTT | 317 |
rs748302396 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708997 | AACTCATGTTGTCTA[C/T]AAGAGTGATTCAGAC | 317 |
rs748311911 | snp | A/C | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725442 | GATCTCCTTTTGCCA[A/C]TTCATGAATTGAGGG | 317 |
rs748311918 | snp | G/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730524 | TGAAATAAAGCAGCA[G/T]AATAGGTTTACATAG | 317 |
rs748315424 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659334 | TTCTGATGCTTCGCA[A/G]ACACCCAAGGTACCG | 317 |
rs748318435 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661017 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCTAGTAG | 317 |
rs748323907 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677105 | TCATTATTAATGTAT[-/C]AAAGGAAAATGGAAA | 317 |
rs748354219 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687868 | CCAGGCTGGAGTACA[A/G]TGGTGTGATCTTGGC | 317 |
rs748366980 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | APAF1 | GRCh38.p7 | 12:98703543 | CTGGGTTTCCAGAGA[A/T]CAAAGGATGACAGAG | 317 |
rs748418506 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649114 | ATGTGTTTATAGAGT[A/T]TATAGGAAAAAATAA | 317 |
rs748440240 | snp | A/G | 1.76846e-05 | 0.00297354 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644691 | TTCTTCCGGCTCTTC[A/G]CCTCAGACATGTCTG | 317 |
rs748446850 | in-del | -/G | 2.04121e-05 | 0.00319463 | upstream-variant-2KB, frameshift-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644612 | GCTGCTCCGGGCCAC[-/G]GGGGTCTTCCCGCCC | 317 |
rs748469927 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728120 | CAGTGGCAGGGATGC[C/T]CTCAATCCAGAGCTG | 317 |
rs748472037 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719146 | CCAGACTGTACCTCA[-/C]ACTCAGTGTCTCCTG | 317 |
rs748521309 | snp | C/T | | | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648653 | CAAAGAGCAGCTATG[C/T]TGATTAAAATGATAC | 317 |
rs748533847 | in-del | -/CGCTCGGTCGC | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643846 | TTTGAGACGGAGTCT[-/CGCTCGGTCGC]CCAGGCTGGAGTGCA | 317 |
rs748556478 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650368 | GTGAGCACCTGTAAT[A/C]CCAGCTACTCGGGAG | 317 |
rs748600489 | snp | C/T | 1.65162e-05 | 0.00287365 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665718 | CTATAAGTGTTGAAA[C/T]GCTCAGAGAAGACAT | 317 |
rs748622554 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715652 | TTTTAAACACATTAC[A/G]TTGGGCATACATTCA | 317 |
rs748647427 | in-del | -/ATCA | 6.84744e-05 | 0.00585086 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735558 | TGTAAATTCAATTCT[-/ATCA]ATCAAAATTTTCTGA | 317 |
rs748652555 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713547 | AACAAGACCAAATAG[A/G]TAAAAATAGAAACAC | 317 |
rs748713197 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664970 | TTGGACATTGTTTAC[A/G]TTGTTTAAGATTTTT | 317 |
rs748713336 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680961 | TTTTTTAATTTGCTT[A/G]TGAACTGGCTTATAT | 317 |
rs748739981 | snp | C/T | 0.000263604 | 0.0114775 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703410 | CTATTGGGAGAAATC[C/T]ACACGGGCCATCACA | 317 |
rs748754370 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664311 | CGTGAGCCACCACAC[C/G]TGGCCAGTTTTGTTA | 317 |
rs748759076 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716745 | TTCTTTGATTCTTTC[C/G]TTTTTGTTCCAGTTT | 317 |
rs748794901 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644967 | TATTGCTCCAAATCC[A/G]AGGAAATTCAAACTC | 317 |
rs748810396 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718399 | ATCACATGCAGCTAA[-/T]TTTTTTTGTATTTTT | 317 |
rs748814087 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687846 | TGAGACAGTCTCACT[C/T]TGTCGCCCAGGCTGG | 317 |
rs748863900 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733065 | AAAAATATTGTGTCT[A/G]TGTGCATAGTCTGCA | 317 |
rs748879722 | snp | C/G | 3.29723e-05 | 0.00406018 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671539 | TTTATTTGTAGGATT[C/G]TGCAGTCAGTGAGAA | 317 |
rs748915330 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727240 | AAGAAGGAGCTGCTA[C/T]CCATGGAGGCTGGGT | 317 |
rs748926828 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681359 | GAGCCACTGTGCCCC[G/T]CCAGAGAGTAATTTT | 317 |
rs748928789 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697105 | TCTCATTTTGTACTT[C/T]AGCTTATGCTGATCC | 317 |
rs748972679 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717432 | CTAGGCTGGAGTGCA[A/G]TGGTGCGACCTTGGC | 317 |
rs748981340 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734102 | AATGGCATTGTGAAT[C/G]CCATTCTTTTAATGA | 317 |
rs748983930 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682442 | TCAATTTCCTGCTAC[A/G]GCTTGCAGGGTTAAG | 317 |
rs749009060 | snp | A/C | 1.65899e-05 | 0.00288005 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665559 | TTTTTAAAGGCTCTC[A/C]CCTTGTAGTATCTTT | 317 |
rs749017270 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661160 | CCCACCTTGGCCTCC[A/C]AAAGTGCTGGGATTA | 317 |
rs749018529 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696240 | CCTGATGAGGGCCTT[C/T]GGCTGCTTCCACTCA | 317 |
rs749023240 | snp | A/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643686 | TTTGTAGCTTTACCA[A/T]ATTCAATCTGTAACT | 317 |
rs749040226 | snp | A/G | 1.66999e-05 | 0.00288958 | intron-variant | APAF1 | GRCh38.p7 | 12:98727362 | ATAATAGCCTATATC[A/G]TACTTTCCAAGCTAT | 317 |
rs749052401 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658863 | AGGTTTAGAAACTGT[A/G]CTGTGCAGTGATCAC | 317 |
rs749072022 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689067 | TAGTCTGCCTGCCTT[-/G]GCCTCCTGAAGTGCT | 317 |
rs749082504 | snp | A/G | 6.63735e-05 | 0.00576041 | intron-variant | APAF1 | GRCh38.p7 | 12:98648610 | GTTGTATACTAAACT[A/G]CTTAATTTTTTTTAG | 317 |
rs749088101 | in-del | -/C | 1.66868e-05 | 0.00288845 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686763 | CTTTGGGATTTGAAT[-/C]AAAAAGAATGTCGAA | 317 |
rs749119537 | in-del | -/AT | 1.64757e-05 | 0.00287012 | intron-variant | APAF1 | GRCh38.p7 | 12:98715578 | GGATGAACTCTTAAC[-/AT]ATTTAATGCTGATTC | 317 |
rs749134752 | snp | G/T | 1.65192e-05 | 0.00287391 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648737 | GGATATAAAGATCTT[G/T]CTGCCCTTCTCCATG | 317 |
rs749168519 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683181 | ACTAGTACACACCTA[C/T]GATGAGCACTCAGAG | 317 |
rs749217205 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723537 | AACAGCCAGTGTATT[A/G]AAACTCTTGTTTTAT | 317 |
rs749220581 | snp | A/G | 1.67419e-05 | 0.00289321 | intron-variant | APAF1 | GRCh38.p7 | 12:98712468 | TCAGAATCTTTCTGT[A/G]CAGAATTAAATAAAA | 317 |
rs749221771 | snp | C/T | 3.35632e-05 | 0.0040964 | intron-variant | APAF1 | GRCh38.p7 | 12:98666387 | GTTTACTTTTTTTTT[C/T]CCTTTTTCCTTTGAA | 317 |
rs749234735 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673901 | TTTGGCTTGGAAAAA[G/T]GAGGAATTCAAGGGA | 317 |
rs749268221 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708808 | ATAATTATTTTGTAT[C/T]TAACAGGTGTCCAGC | 317 |
rs749284479 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | APAF1 | GRCh38.p7 | 12:98683300 | ATATTGAGAATTAGG[C/T]AGATAAATTTGATTC | 317 |
rs749288279 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675082 | ATGTTCTCTCATAGA[A/G]TGGTTAGCTATTTAT | 317 |
rs749370222 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718934 | GCAAGTCCCCATCTC[-/A]AATATATAATGGCCT | 317 |
rs749374846 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725555 | GGTAGGCTGTTTGCT[A/G]ACATGAGAGCACTGC | 317 |
rs749384246 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722362 | TCTTTGCTAAACTCT[C/T]AAGTTTCTTTATGCT | 317 |
rs749387431 | snp | A/G | 3.29506e-05 | 0.00405884 | intron-variant | APAF1 | GRCh38.p7 | 12:98706449 | CTTCAAAATGCTTAT[A/G]TATGTGATTTCCTAT | 317 |
rs749410709 | snp | A/T | 1.76871e-05 | 0.00297375 | intron-variant | APAF1 | GRCh38.p7 | 12:98662611 | ACCTTTATATTTAAT[A/T]TAATTACATTTAAAT | 317 |
rs749412360 | snp | A/G | 3.30006e-05 | 0.00406192 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662471 | GTCTCTCTTGATCTT[A/G]GATGATGTTTGGGAC | 317 |
rs749452333 | snp | A/G | 3.57136e-05 | 0.00422558 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644749 | AGCTTCTTCACCAGG[A/G]GGAGCAGGACGTGGC | 317 |
rs749455435 | snp | A/G | 1.6607e-05 | 0.00288153 | intron-variant | APAF1 | GRCh38.p7 | 12:98708536 | TCGCTTTAAGATGAA[A/G]ACATGTTATTTTAGA | 317 |
rs749487254 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715524 | ATGAGAAGACTCTTA[C/T]TTCAAGTTCTGATGA | 317 |
rs749499327 | in-del | -/TC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674441 | TGTGAAGTGGAGGTC[-/TC]TCTCTCTCTCTCTCT | 317 |
rs749506128 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700002 | CACCTACAATTTTAT[A/G]ATTTGATGACTCTGA | 317 |
rs749506718 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701669 | AGGAAGATAATTTTA[A/T]ATTGCATGAAATGCC | 317 |
rs749508732 | snp | A/G | 1.75065e-05 | 0.00295854 | intron-variant | APAF1 | GRCh38.p7 | 12:98680247 | GTTAAGCAGTTTATT[A/G]TAAAAAATATTTTAT | 317 |
rs749575227 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648452 | GGATCACATGATTAG[C/T]GATGGATTTTTAACA | 317 |
rs749581921 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648955 | TAGTGATGTTTTCAA[C/T]TTAAATATTTTTTAT | 317 |
rs749631286 | in-del | -/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688639 | TCACACCTGGCGAAA[-/TTT]TTTTTTTTTTTTTTT | 317 |
rs749666725 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664792 | CTCCCACCTCAGCCT[C/G]CTGAAGTGCTAGGAC | 317 |
rs749682848 | snp | A/C | 3.36304e-05 | 0.0041005 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680378 | CAGATTTATAGCAAC[A/C]TGCTCAGTGGATAAA | 317 |
rs749704574 | snp | C/G | 1.64909e-05 | 0.00287144 | intron-variant | APAF1 | GRCh38.p7 | 12:98666141 | TACCTGTCTACAGTC[C/G]TGGTCATTGTACTTT | 317 |
rs749757628 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649543 | GTTGTTTTTGTCACA[A/G]GGAAGAAGCTGGTGA | 317 |
rs749807311 | snp | G/T | 1.70905e-05 | 0.00292318 | intron-variant | APAF1 | GRCh38.p7 | 12:98723623 | AACCTCCAAGTGTTT[G/T]TTTTTTTTTTTTAAG | 317 |
rs749813416 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678598 | AGGACCCCTTCCCCC[-/T]GGTGCAGCTGTAGCT | 317 |
rs749857661 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722922 | TTTTTTTTTTCTATC[A/T]TCTGGTATAATTAAC | 317 |
rs749865792 | snp | C/G | 1.99277e-05 | 0.00315649 | intron-variant | APAF1 | GRCh38.p7 | 12:98649709 | TTAGTCCATTTCATA[C/G]TCTAGTAAGGTAGAT | 317 |
rs749924325 | in-del | -/AAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658301 | TATGGCTCAATTAAC[-/AAT]GATGATGATAACAGT | 317 |
rs749924784 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644788 | CGTTCGTGGGAACCC[G/T]GGGCGGTGACCGCGC | 317 |
rs749932082 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651162 | TTTTGTGGGATCTCA[A/G]GTTCAGAGGACTGAG | 317 |
rs749938985 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652556 | TTCCAATTTTTTTTT[A/C]TTTTTGCTTTTTAGG | 317 |
rs749978738 | snp | C/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643487 | GCTATTCCCTCCTCC[C/T]GCCAGAAAAAAAAAG | 317 |
rs749986237 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706531 | CTGATTGCAGAGGAC[A/G]TTTAAGTTGGGTTCA | 317 |
rs749988551 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725504 | CTCTGTGGACAGTAC[C/T]CTGCTGGCAACGGGA | 317 |
rs750033912 | in-del | -/AG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713079 | CCATCTTGGCCTCCC[-/AG]AGTGTTGGGATTACA | 317 |
rs750038068 | snp | C/T | 3.47977e-05 | 0.00417105 | intron-variant | APAF1 | GRCh38.p7 | 12:98677386 | AGTTACTTTTACTCT[C/T]ATTTATTTAATTTCT | 317 |
rs750066592 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725104 | AATCTAGTGAACAGT[G/T]GAGCTAGCACTCACA | 317 |
rs750071482 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722459 | ATTTGAAGTCAAGTA[-/T]TAATAAAGCTCTAAA | 317 |
rs750082321 | in-del | -/A | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646148 | ATATTTTAGTTTAAC[-/A]GGACTAGGTGAAATT | 317 |
rs750120603 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723327 | GGTAATTTAAAGTAT[A/T]AATTTGTTTTTTGAA | 317 |
rs750148711 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658818 | GTCCCTTACAACAAA[C/G]AATTGCCATCCCAAA | 317 |
rs750162239 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676265 | CCCAGGCTGGAGTGC[A/G]GTGGTATGATCTTGG | 317 |
rs750195115 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688750 | TAGGCGTGAGCCACC[A/G]AGCCTAGCCTACCAC | 317 |
rs750196538 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651069 | GTTATCTTGGAACAG[A/G]TTTTAACTACTTTGT | 317 |
rs750207615 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698765 | ACTGCTCATGGCCCA[A/G]AGGAGTGAAGGTGGA | 317 |
rs750250344 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689817 | TTTGGTTCTGAGTAC[A/G]TATATCTATCTATAT | 317 |
rs750252310 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674791 | ATATATGTATATAAA[C/T]GTATAGACATACATA | 317 |
rs750269514 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672212 | CTATGTTGCCAAGGC[C/T]GGAGTGCAGTGGTGT | 317 |
rs750311065 | snp | G/T | 1.65384e-05 | 0.00287557 | intron-variant | APAF1 | GRCh38.p7 | 12:98649472 | CATTCATGCTTGTTT[G/T]GTTTTGGATTTTAGT | 317 |
rs750361334 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant | APAF1 | GRCh38.p7 | 12:98723148 | CCCCTCCAATGAGAT[A/G]GGATCGGGGGAGGAT | 317 |
rs750362945 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701412 | ATTTATTTAGTTTTC[C/T]GAGGAACCACTAGAT | 317 |
rs750363951 | snp | C/G | 1.65239e-05 | 0.00287431 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649629 | ACATGGAATGGCAGG[C/G]TGTGGGAAGTCTGTA | 317 |
rs750365782 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702542 | AAATTGAAGAAACTG[A/C]GGCTGGGCGTGGTGG | 317 |
rs750367842 | snp | G/T | 1.66693e-05 | 0.00288693 | intron-variant | APAF1 | GRCh38.p7 | 12:98723352 | TTTGAAAAAGTATTC[G/T]CATATTGCAATGATT | 317 |
rs750427694 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650101 | CATCAGTTCTAGGCT[G/T]CCCCCATTCATCAGT | 317 |
rs750438876 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727856 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 317 |
rs750450897 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715124 | CACTTGTTTGATGAA[A/G]TGGGTAGTTGAGTAC | 317 |
rs750464153 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664301 | GGATTACAGGCGTGA[A/G]CCACCACACGTGGCC | 317 |
rs750475464 | snp | C/G | 1.64776e-05 | 0.00287028 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727283 | CTTTTCTCCAGATGG[C/G]AAAATGCTTATCTCT | 317 |
rs750478743 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680461 | CATTTTATTTTTCCA[C/T]GATCATGAGACCAGA | 317 |
rs750495766 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715363 | TTAGTTTAATATCTT[C/T]GGGGTGTAATGCCTA | 317 |
rs750499402 | snp | A/T | 1.67514e-05 | 0.00289403 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662777 | CAGATTTGCCAGAAC[A/T]AGCTCATAGTATTAT | 317 |
rs750507815 | snp | A/G | 9.885e-05 | 0.0070296 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671618 | ATTTCCTAATATTGT[A/G]CAACTGGGTCTCTGT | 317 |
rs750536014 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685797 | TGGGCCACCACTCCC[A/C]GCTAATTTTTTGTGT | 317 |
rs750553739 | in-del | -/CTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716973 | TGGGTTCAGGCAATT[-/CTC]CTGGCTCAGCCTCCT | 317 |
rs750610991 | snp | C/T | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729560 | GCCACAGACCAGTAC[C/T]GGTCCATGGCCCAGG | 317 |
rs750635443 | snp | A/G | 3.30077e-05 | 0.00406236 | intron-variant | APAF1 | GRCh38.p7 | 12:98712270 | CTGTTCTGACGAACA[A/G]AAACTGCTCTTACAG | 317 |
rs750647611 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon, missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732428 | TGAACAGTGGTGGAA[C/T]GTTGTCACTGGGGAA | 317 |
rs750664698 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679139 | CTGCCCATGGACCAG[C/T]TGGCATGTACTTCCT | 317 |
rs750688002 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712373 | GAAGCTCAAGTTAGC[C/T]GCTGTTGCTTAAGTC | 317 |
rs750711057 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695149 | CCTCTGCCTTTTGGG[G/T]TCAAGCAGTTCTCCT | 317 |
rs750738247 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660205 | ACAAAAATTAATCTG[A/G]TGTGGTGGTACACAC | 317 |
rs750740410 | snp | C/T | 1.66751e-05 | 0.00288744 | intron-variant | APAF1 | GRCh38.p7 | 12:98648833 | TTGTATCCATTATAC[C/T]TTCTATCACTTTGCT | 317 |
rs750808870 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683249 | ATCTTCTCTTAGCCA[C/G]TGGGTCAAGTGACTG | 317 |
rs750874670 | in-del | -/TCT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656590 | AAATTCTGATCTAAG[-/TCT]TCTTCTGTCATTCCT | 317 |
rs750892155 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688935 | CTCCCACCTCAGCCT[C/G]TTGAGTAGCTGGGAC | 317 |
rs750944458 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719966 | AGCAGTATGATTGCA[A/G]TGAAATTTGGCTTTA | 317 |
rs750959260 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659305 | TATTGAAGAGGCTAA[A/G]GACCGTCTCCGCATT | 317 |
rs750983482 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697863 | CTATAACTTTTTAAG[C/T]ATTTTGTAGGGTATC | 317 |
rs750995933 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674618 | TCTGAAGTATAGAAT[A/G]GTTTGGAGGTTAAAA | 317 |
rs750996873 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667612 | TGGTACAACTTTCTG[A/G]CCTATCACATGGCCA | 317 |
rs750997348 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705581 | AGTAGTTCTGTAATT[C/T]AAAGTGTAATGAGAG | 317 |
rs751014484 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724958 | TAACATTTAAAGATT[A/G]CTTGTCACATGCTAG | 317 |
rs751017701 | snp | A/T | 1.64931e-05 | 0.00287163 | intron-variant | APAF1 | GRCh38.p7 | 12:98725392 | GTTTATAGCATTGCT[A/T]AACAATCCTAATTGC | 317 |
rs751032444 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650091 | TGTATAGCTCCATCA[A/G]TTCTAGGCTGCCCCC | 317 |
rs751034271 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657248 | TGATTCCAGAATATC[C/G]TCTCTATTCATACTA | 317 |
rs751040856 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719517 | ACCATTTCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 317 |
rs751049273 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658657 | ATCAGTAGTTCTCAA[C/G]GAGGGGTGATTTCAC | 317 |
rs751071524 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648426 | AAGGACATCAAGACA[C/T]CCTACATCATGGATC | 317 |
rs751102050 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | APAF1 | GRCh38.p7 | 12:98677561 | TTACAGGTAAAACAC[A/G]TCTCTTGAGAAAAAT | 317 |
rs751106475 | snp | A/T | 1.74096e-05 | 0.00295034 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680345 | TGAAGTGCTTTGTTG[A/T]GCATTCTCTACAGAT | 317 |
rs751118837 | in-del | -/AAC | | | intron-variant, cds-indel | APAF1, ANKS1B | GRCh38.p7 | 12:98729942 | AGGGAAATTATAGTT[-/AAC]AATTTATTGTATATT | 317 |
rs751127168 | in-del | -/AAGAACTCTGCTGTAATGTTA | 1.65299e-05 | 0.00287483 | cds-indel, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708609 | ACAAAGAAAGTATGT[-/AAGAACTCTGCTGTAATGTTA]AAGCAAGAAGTAGAT | 317 |
rs751135737 | snp | A/G | 3.30628e-05 | 0.00406575 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708597 | CAGCTCTGGGAGACA[A/G]AGAAAGTATGTAAGA | 317 |
rs751172038 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667605 | TATGTATTGGTACAA[-/CT]TTCTGGCCTATCACA | 317 |
rs751211976 | snp | A/G | 1.70909e-05 | 0.00292321 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735641 | AAGAAGATCCTGTAA[A/G]AAAGAGAATTCATTT | 317 |
rs751223111 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | APAF1 | GRCh38.p7 | 12:98723156 | ATGAGATAGGATCGG[A/G]GGAGGATTATAACAG | 317 |
rs751248548 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723120 | TTAGACAAGAGAATG[C/T]ACACTCTCTCCACCC | 317 |
rs751280166 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673524 | TGTCATGCTTCCCTT[A/G]CAGCTTGAAATAATA | 317 |
rs751284404 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648255 | GTTTCTTGTTTATTA[A/G]TGAGATTATGTATCT | 317 |
rs751307468 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688440 | CTAAGTTCAGAGATA[C/G]TAGAATAACCTTCTA | 317 |
rs751333239 | in-del | -/TG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722900 | AGCTCACTGGCATAT[-/TG]TGTGTTTTTTTTTTT | 317 |
rs751350338 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701044 | CATACAGCCTTGTTG[C/T]AACCAATGTACAGAT | 317 |
rs751404478 | snp | A/G | 1.69522e-05 | 0.00291132 | intron-variant | APAF1 | GRCh38.p7 | 12:98723599 | ATATAAAATGTTCTT[A/G]AAAGTGTCAACCTCC | 317 |
rs751423061 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662148 | GATAGTAATGGTCGC[-/TT]TTTTTTTTTTTTTTT | 317 |
rs751439895 | snp | C/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730472 | ATAAGATGTTACAAA[C/G]ATCAGTGACCATATT | 317 |
rs751481863 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676384 | CTGCTAATTTTTGTA[-/T]TTTTAGTAGAGATGG | 317 |
rs751482366 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692501 | TTTGGGTACAACTGG[C/T]CCTGTCATCCAGATA | 317 |
rs751492751 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714679 | TTGTTTTCAAGGGGC[A/T]TTTCTTCCAGACGTG | 317 |
rs751516302 | snp | C/T | 9.05059e-05 | 0.00672642 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644533 | CTTACCAGGCCAGGC[C/T]CAGGCACGTCCCCAG | 317 |
rs751530547 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713083 | CTTGGCCTCCCAGAG[C/T]GTTGGGATTACAGGC | 317 |
rs751559179 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664058 | CGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 317 |
rs751568034 | in-del | -/T | 0.0114066 | 0.0746537 | intron-variant | APAF1 | GRCh38.p7 | 12:98662438 | CATTAGTGATTAATA[-/T]TTTTTTTTTTAAATT | 317 |
rs751585974 | snp | C/T | 3.35796e-05 | 0.0040974 | intron-variant | APAF1 | GRCh38.p7 | 12:98699604 | AACTTCAGTCTGATT[C/T]AAAGAAAGTTAAAAC | 317 |
rs751592519 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677976 | ATTTCCTAAGTTGTT[C/T]TAAAGAATTTCCTTT | 317 |
rs751614473 | snp | A/C | 1.651e-05 | 0.0028731 | intron-variant | APAF1 | GRCh38.p7 | 12:98671489 | ATGGAAAAATGTCAG[A/C]TCGTGGCTCTGATTG | 317 |
rs751620088 | snp | C/G/T | 8.26513e-05 | 0.00642804 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712428 | GAGATGAAAATGGAG[C/G/T]CATTGAGGTATTCAG | 317 |
rs751642711 | in-del | -/TATC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685033 | CTGAAGAATTGAGTT[-/TATC]TAGGACTGGGATAAA | 317 |
rs751656516 | in-del | -/TTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676210 | ACATTCCTTTACACC[-/TTA]TTATTTATTTATTTA | 317 |
rs751718621 | snp | A/G | 2.18912e-05 | 0.00330834 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732563 | TTTACAGACTTTAGA[A/G]TAAAATAGTTAAGCA | 317 |
rs751721415 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683273 | GTGACTGCTTCCTCA[A/G]AGTAAGTGTGGATAT | 317 |
rs751796312 | snp | C/T | 1.66788e-05 | 0.00288775 | intron-variant | APAF1 | GRCh38.p7 | 12:98648836 | TATCCATTATACCTT[C/T]TATCACTTTGCTATC | 317 |
rs751846665 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706816 | ATTACCATGGGCCAA[A/G]TGCTGTGGGAACTTC | 317 |
rs751875283 | snp | A/G | 1.6537e-05 | 0.00287545 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686776 | ATCAAAAAGAATGTC[A/G]AAATACCATGTTTGG | 317 |
rs751896428 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686847 | GATAAGCTTTTGGCT[A/G]GTTGTTCAGCTGATG | 317 |
rs751898239 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656119 | TTTTTTTAGGGACGT[A/G]GTTTCACCATGTTGC | 317 |
rs752007246 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682344 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTGATGAT | 317 |
rs752038243 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646140 | AGATTTGCATATTTT[A/G]GTTTAACAGGACTAG | 317 |
rs752069194 | snp | G/T | 1.6729e-05 | 0.00289209 | intron-variant | APAF1 | GRCh38.p7 | 12:98662591 | TTATTCGTTTACTTT[G/T]TAGTACCTTTATATT | 317 |
rs752094345 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734014 | GGCCAATTTTAATCA[C/T]AAGCCTTAATAAGAT | 317 |
rs752116281 | snp | A/G | | | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735621 | TGCCCGGTATGGCTG[A/G]CATGAAGAAGATCCT | 317 |
rs752145548 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735113 | GAAAGACAAGGTAAC[A/G]TGAAGAAAGAAGAGA | 317 |
rs752149600 | snp | A/C | 3.30863e-05 | 0.00406719 | intron-variant | APAF1 | GRCh38.p7 | 12:98727151 | TAACTCTGTTAATGA[A/C]TTGTGTATCATGTTT | 317 |
rs752153806 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706563 | GGTGTGATGTTTTCT[C/T]CTGATGGATCATCAT | 317 |
rs752161586 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671371 | CTATGTTTAAAAGTC[A/G]GAAGAGGATTACTAT | 317 |
rs752227133 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666232 | ACTGAAGAAGTTGAA[G/T]ACATACTGCAGGAGT | 317 |
rs752231166 | snp | A/T | 2.19277e-05 | 0.00331109 | intron-variant | APAF1 | GRCh38.p7 | 12:98683115 | GAAAATAATGGATAT[A/T]TGTAAATTTTTTCTC | 317 |
rs752239491 | in-del | -/TCTTCAGAATCTTTC | 1.66095e-05 | 0.00288175 | intron-variant | APAF1 | GRCh38.p7 | 12:98712450 | GGTATTCAGTGCTAG[-/TCTTCAGAATCTTTC]TGTACAGAATTAAAT | 317 |
rs752257720 | in-del | -/C | 1.64768e-05 | 0.00287021 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723727 | TTTCTCACGATGCTA[-/C]CAAGTTTTCATCTAC | 317 |
rs752299349 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | APAF1 | GRCh38.p7 | 12:98659157 | TATTCTTTCCCTCAC[G/T]AGGTTGTTTCCCAGG | 317 |
rs752314764 | snp | G/T | 1.87943e-05 | 0.00306542 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735526 | ATCAACCTTTCTATT[G/T]AGGCTTTATCAGCTA | 317 |
rs752327456 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648091 | TAAACAATTCCATAT[C/G]TTACTGCTTTCCAGA | 317 |
rs752330919 | snp | C/G | 1.692e-05 | 0.00290856 | intron-variant | APAF1 | GRCh38.p7 | 12:98723611 | CTTAAAAGTGTCAAC[C/G]TCCAAGTGTTTTTTT | 317 |
rs752338425 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700969 | ATAATATTCCATTGT[A/G]TGTATATATCACATT | 317 |
rs752354073 | snp | A/G | 3.29837e-05 | 0.00406088 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666311 | GTTATTATTTACATG[A/G]TCTTCAAGTAGATTT | 317 |
rs752406917 | snp | G/T | | | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644570 | CAGGCTCAGGCACGT[G/T]CGGGGGTCTGCCCAG | 317 |
rs752422240 | snp | A/C | 3.55095e-05 | 0.00421349 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644546 | GCCCAGGCACGTCCC[A/C]AGCGACAGCAGGCTC | 317 |
rs752439595 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724006 | TAATCAAATGCAACC[C/T]CTACTGCATATTGTA | 317 |
rs752466423 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699392 | ACTTTTTCTTTTTTA[C/T]TACTTTAATTCAAAG | 317 |
rs752511035 | snp | G/T | 4.95438e-05 | 0.00497689 | intron-variant | APAF1 | GRCh38.p7 | 12:98703328 | GAATAGCTTATCTCT[G/T]AAAGTATTTTACCTT | 317 |
rs752512193 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659280 | GTTTTTCCCAGAGGC[C/T]TCCACTTAATATTGA | 317 |
rs752522022 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644859 | CCTCTCCCCGGCATC[A/C]TCGTTGCTTCACTGA | 317 |
rs752560095 | snp | C/T | 3.29576e-05 | 0.00405928 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703427 | CACGGGCCATCACAG[C/T]ACCATCCAGTACTGT | 317 |
rs752560323 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646658 | GGGAGGGGCACAAAT[A/G]TGTATTGAATGAATG | 317 |
rs752561648 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688638 | TCACACCTGGCGAAA[-/TT]TTTTTTTTTTTTTTT | 317 |
rs752587169 | in-del | -/ATAAAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672633 | ATCTTACCTTTCCTT[-/ATAAAA]AGGAAAGGATAGCTA | 317 |
rs752612461 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671638 | TGGGTCTCTGTGAGC[C/T]GGAAACTTCAGAAGT | 317 |
rs752622248 | snp | A/G | 8.27287e-05 | 0.00643098 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732483 | GGAACCAATCTTAAG[A/G]AAATACACGTGTCCC | 317 |
rs752637333 | snp | C/T | 1.98553e-05 | 0.00315075 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644617 | TCCGGGCCACGGGGG[C/T]CTTCCCGCCCTCGCT | 317 |
rs752662545 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727398 | CTTCCTGTTTCTCAG[C/T]TGGGCCTTTTACAAC | 317 |
rs752707499 | in-del | -/CTG | | | utr-variant-3-prime, cds-indel, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732963 | CAGGGTAGCAGTGGC[-/CTG]CTTTTTGAACCACAC | 317 |
rs752715933 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729034 | CAGTCTATGGGGGAA[A/G]CAGGTGGTAAACCAA | 317 |
rs752721543 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690200 | ATCTTGCTTTGCTGA[C/T]GGAAGATAACTGTTT | 317 |
rs752738676 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686809 | ATACAAATTCAGTCA[A/G]TCACTGCAGATTTTC | 317 |
rs752792108 | snp | G/T | 3.30038e-05 | 0.00406212 | intron-variant | APAF1 | GRCh38.p7 | 12:98667649 | AGATGCACAAGGTAA[G/T]ATGACCCATTTAAAA | 317 |
rs752844788 | snp | A/C | 1.64972e-05 | 0.00287199 | intron-variant | APAF1 | GRCh38.p7 | 12:98723146 | CACCCCTCCAATGAG[A/C]TAGGATCGGGGGAGG | 317 |
rs752986176 | snp | A/G | 5.0929e-05 | 0.00504598 | intron-variant | APAF1 | GRCh38.p7 | 12:98671104 | ATATATATTAACATG[A/G]AAAATTAGTGCTAAA | 317 |
rs753009072 | snp | C/G | 4.94181e-05 | 0.00497057 | intron-variant | APAF1 | GRCh38.p7 | 12:98725548 | AAATCAGGGTAGGCT[C/G]TTTGCTGACATGAGA | 317 |
rs753017289 | snp | A/G | 1.64923e-05 | 0.00287156 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98670988 | GAACTTTGTGCTTTA[A/G]TGTTTTCCCTGGATT | 317 |
rs753038475 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711526 | TTAAGGAAAAACTAC[C/G]TGTGATTGGTTGACT | 317 |
rs753042213 | snp | A/G | 0.00027464 | 0.0117152 | intron-variant | APAF1 | GRCh38.p7 | 12:98662602 | CTTTTTAGTACCTTT[A/G]TATTTAATTTAATTA | 317 |
rs753069459 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681958 | AAAATCCCAGTGAAG[G/T]TTCATTAGGTAATTT | 317 |
rs753084099 | snp | C/T | 1.65318e-05 | 0.002875 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708614 | GAAAGTATGTAAGAA[C/T]TCTGCTGTAATGTTA | 317 |
rs753107484 | in-del | -/TTAT | 5.1272e-05 | 0.00506294 | intron-variant | APAF1 | GRCh38.p7 | 12:98662813 | AATGTAAAGGTATGG[-/TTAT]TTATTTGTTTATGAG | 317 |
rs753124446 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682980 | AGGCAAAATATTGCC[A/G]TATTTTAGAAAGGGG | 317 |
rs753139253 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696018 | TGCTGCTGTCTCTTT[C/T]TCCATTTTCCTTCGC | 317 |
rs753148886 | snp | A/G | 6.66889e-05 | 0.00577408 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662723 | TAGGAAAGGAAAAAG[A/G]ACTTGAAATTTTATC | 317 |
rs753152882 | in-del | -/AATGAAATAT | 1.64732e-05 | 0.0028699 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671656 | AACTTCAGAAGTTTA[-/AATGAAATAT]TCAGCAAGCTAAGCT | 317 |
rs753165073 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648435 | AAGACATCCTACATC[A/G]TGGATCACATGATTA | 317 |
rs753193091 | in-del | -/GGG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704522 | TACTGTGAAGGTGTT[-/GGG]GGAGAGTTGCTAAGC | 317 |
rs753203820 | snp | A/G | 1.66385e-05 | 0.00288426 | intron-variant | APAF1 | GRCh38.p7 | 12:98648530 | AGTCCACACTTCCTT[A/G]AAAATTTTTAGAATT | 317 |
rs753241888 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699328 | GAATAAGTTTATGTG[G/T]CATTTAATTTAGGAA | 317 |
rs753246030 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709342 | ACAAAGAGTGGGACA[C/T]GTGAGAGGAAGGCAT | 317 |
rs753300065 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683483 | GGAGCATGGCTTCAG[G/T]CATAGCTGACTCCAA | 317 |
rs753313527 | snp | A/T | 0.00027998 | 0.0118284 | intron-variant | APAF1 | GRCh38.p7 | 12:98708712 | GTCTGCAAGTGAGTA[A/T]TTTTTAGAAAACAAT | 317 |
rs753320288 | snp | A/T | 1.69991e-05 | 0.00291535 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680359 | GTGCATTCTCTACAG[A/T]TGACAGATTTATAGC | 317 |
rs753365647 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688641 | ACACCTGGCGAAATT[-/T]TTTTTTTTTTTTTTT | 317 |
rs753375465 | snp | A/C | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646460 | ATTTGGTGACTTCAA[A/C]AACAGTCATTGAAGC | 317 |
rs753417958 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723736 | ATGCTACCAAGTTTT[C/T]ATCTACCTCTGCTGA | 317 |
rs753427373 | snp | A/T | 1.65089e-05 | 0.00287301 | intron-variant | APAF1 | GRCh38.p7 | 12:98703338 | TCTCTTAAAGTATTT[A/T]ACCTTCATAGGTATC | 317 |
rs753433659 | snp | C/T | 1.84289e-05 | 0.00303548 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644637 | CCGCCCTCGCTCCGC[C/T]TCCCGGGCTCCGCAG | 317 |
rs753489861 | snp | C/G | 6.58968e-05 | 0.00573969 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659285 | TCCCAGAGGCTTCCA[C/G]TTAATATTGAAGAGG | 317 |
rs753512898 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705363 | CTCAAGGGAGATTTT[-/C]AGTTTCTTAGGAGAG | 317 |
rs753598795 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726780 | TACATTAAAAAAATT[A/T]TTTTCTCCCTGATTA | 317 |
rs753610838 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661638 | GTGCCACCTCGCCTG[A/G]CTAATATTATATTAG | 317 |
rs753611857 | in-del | -/CACTTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724376 | GGTCTGCACCTCTTC[-/CACTTT]ATCTTCCATACCACT | 317 |
rs753659629 | snp | A/G | 1.66366e-05 | 0.0028841 | intron-variant | APAF1 | GRCh38.p7 | 12:98671766 | TGGTGCGCTAACTAT[A/G]TCATTATTTTTCAGG | 317 |
rs753672795 | snp | C/G | 1.77413e-05 | 0.00297831 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644722 | GAGACCCTAGGACGA[C/G]AAGCCCAGGGCAGCT | 317 |
rs753677497 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677634 | TTAAATCCTAAAATT[C/T]AAGAAAATTGCAACT | 317 |
rs753678514 | in-del | -/C | 1.6473e-05 | 0.00286988 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725511 | ACAGTACCCTGCTGG[-/C]CAACGGGAGATGACA | 317 |
rs753697604 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660143 | TTGAGTCCAGGAGTT[C/T]GAGACCAGCATGGGC | 317 |
rs753712744 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677507 | GCCTGCTTTTCTGAG[A/G]ATGGTCAGAGAATAG | 317 |
rs753741775 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725476 | ACAACGGCTGTGTGC[A/G]CTGCTCTGCCTTCTC | 317 |
rs753747121 | snp | C/T | 4.95258e-05 | 0.00497599 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665667 | GAATAAGGAAATCTT[C/T]GTCTTATGATTATGA | 317 |
rs753779358 | in-del | -/AG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669386 | TTTCATTGGAAAAAC[-/AG]AAAAAAACGATGAAA | 317 |
rs753782480 | snp | A/G | 4.97459e-05 | 0.00498703 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665786 | GACGTTAAGGTGCCT[A/G]CAAAGGTAATGGGAT | 317 |
rs753812248 | snp | C/T | 0.000166522 | 0.00912323 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732572 | TTTAGAATAAAATAG[C/T]TAAGCATTAATGTAG | 317 |
rs753853817 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702915 | CAAAAACAGGAAAAT[G/T]ATTGACTATAATGGA | 317 |
rs753853947 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718090 | ATCCCTCATTCTCAG[A/T]ATTGTAATTCTACCC | 317 |
rs753865642 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715487 | CACAAGAAAACTGTA[C/T]GGCACATCCAGTTCA | 317 |
rs753876879 | snp | C/T | 1.67061e-05 | 0.00289011 | intron-variant | APAF1 | GRCh38.p7 | 12:98648844 | ATACCTTCTATCACT[C/T]TGCTATCAAAATTGC | 317 |
rs753971510 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651636 | GTATTTGTAGCTAGG[A/C]GCAAAATTAGTAATT | 317 |
rs753984114 | snp | G/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732244 | CATCACCAGTGTTCA[G/T]CAGGAAGAGGCTGAC | 317 |
rs754044920 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, intron-variant | APAF1 | GRCh38.p7 | 12:98727184 | GTAGATATGGAATGT[C/T]TCAAACGGTGAGCTT | 317 |
rs754050351 | snp | A/G | 1.78398e-05 | 0.00298657 | intron-variant | APAF1 | GRCh38.p7 | 12:98671125 | TAGTGCTAAAAAGGA[A/G]TCTCATTTTTTTTTA | 317 |
rs754064256 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666056 | TTGAGGAGTAGCTGA[A/G]TTTCTTCTTAAGAAA | 317 |
rs754108532 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727267 | GGGTGACTGACCTTT[A/G]CTTTTCTCCAGATGG | 317 |
rs754127964 | snp | C/G | 1.75111e-05 | 0.00295893 | intron-variant | APAF1 | GRCh38.p7 | 12:98662843 | TGAGGAGATTATAGG[C/G]AGTTATATAATTTCC | 317 |
rs754166984 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681845 | CCTATTAAAGAACTT[C/T]AAAATAAGATAAACT | 317 |
rs754177684 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658523 | AATCAATGAGACTGA[A/G]GTTAAATGATTTGAT | 317 |
rs754181897 | in-del | -/GGT | 1.649e-05 | 0.00287136 | intron-variant | APAF1 | GRCh38.p7 | 12:98671727 | GAATGGATGTAAGTA[-/GGT]TAGGAGAGAAACCAA | 317 |
rs754190099 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653486 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 317 |
rs754208779 | snp | A/G | 3.331e-05 | 0.00408092 | intron-variant | APAF1 | GRCh38.p7 | 12:98648540 | TCCTTAAAAATTTTT[A/G]GAATTTCAGAACTTG | 317 |
rs754236062 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714376 | ATATGGTGTAGCCTC[A/G]TATCATCAAATAATA | 317 |
rs754256829 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680816 | AAATTAGTGAGTTTG[G/T]CTTCCATTAATAGAC | 317 |
rs754271606 | in-del | -/CCT | 1.64874e-05 | 0.00287113 | intron-variant | APAF1 | GRCh38.p7 | 12:98706662 | TGATGGTGAGCTAAA[-/CCT]CCTACAAACTAAGAA | 317 |
rs754283068 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707094 | TGCAGCTTCTAAGAT[A/G]TTTTTTTTTCATGTA | 317 |
rs754309023 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681526 | TTTTCAAAGGGGTTA[A/T]ATCTGGAGTACTGGA | 317 |
rs754360084 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723027 | CATAACCGCAGCTTC[C/T]GTCTGTAAAATGTGG | 317 |
rs754393240 | in-del | -/TT | 4.94458e-05 | 0.00497197 | intron-variant | APAF1 | GRCh38.p7 | 12:98677556 | AACCTTACAGGTAAA[-/TT]ACACATCTCTTGAGA | 317 |
rs754413122 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708136 | ATTTTTAGTAGAAAT[A/T]GGGTTTCACCATGTT | 317 |
rs754439819 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683230 | TTCACCAACAGTAGT[C/T]ATCATCTTCTCTTAG | 317 |
rs754450904 | snp | A/T | 1.66443e-05 | 0.00288477 | intron-variant | APAF1 | GRCh38.p7 | 12:98665816 | TCAATGATCCTCATC[A/T]TTGGGTATTTATTGC | 317 |
rs754488982 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725315 | GAATTGCCAGATATT[A/G]GAATGTCCATGTGAT | 317 |
rs754498012 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | APAF1 | GRCh38.p7 | 12:98677573 | CACATCTCTTGAGAA[A/G]AATGCAAAGAGGCAT | 317 |
rs754516281 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734222 | TTCCCTTGTCTCTCT[C/T]ATCCTCTTTTCCTTC | 317 |
rs754525727 | snp | G/T | 1.73369e-05 | 0.00294417 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735651 | TGTAAAAAAGAGAAT[G/T]CATTTATTTATTCAC | 317 |
rs754546280 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685779 | TAGCTGGGATTACAG[A/G]CATGGGCCACCACTC | 317 |
rs754547312 | snp | A/C | 1.72874e-05 | 0.00293997 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680348 | AGTGCTTTGTTGTGC[A/C]TTCTCTACAGATGAC | 317 |
rs754555583 | in-del | -/AC | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729883 | AAGGGGTACAAAAAT[-/AC]AGATAAACAAAAGGA | 317 |
rs754575365 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649498 | TTAGTAAGGACAGTC[C/T]TGTGTGAAGGTGGAG | 317 |
rs754625181 | in-del | -/T | 1.65784e-05 | 0.00287905 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708650 | GAAGTAGATGTTGTG[-/T]TTTCAAGAAAATGAA | 317 |
rs754633677 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650503 | AAAAAAAGTTTTTTG[-/T]TTTTTTTTTTTTGAT | 317 |
rs754640492 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683568 | CTTCCTCTGTGTTGG[C/T]TCAGGCATGCTCTTT | 317 |
rs754647777 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666217 | CTCTGGGACATGGAA[A/G]CTGAAGAAGTTGAAG | 317 |
rs754650498 | snp | A/G | 8.24695e-05 | 0.0064209 | intron-variant | APAF1 | GRCh38.p7 | 12:98723157 | TGAGATAGGATCGGG[A/G]GAGGATTATAACAGA | 317 |
rs754661330 | in-del | -/TTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716092 | ATAGTATTACAAGAC[-/TTA]TTATGAAAAACAGAC | 317 |
rs754663602 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98645009 | CAGGCCGACGGGACC[A/C]GAGGAGGAGGGGCAG | 317 |
rs754700839 | snp | A/G | 3.34778e-05 | 0.00409119 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649655 | CTGTATTAGCTGCAG[A/G]AGCTGTTAGAGATCA | 317 |
rs754703778 | snp | A/G | 1.69378e-05 | 0.00291009 | intron-variant | APAF1 | GRCh38.p7 | 12:98723605 | AATGTTCTTAAAAGT[A/G]TCAACCTCCAAGTGT | 317 |
rs754716752 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646500 | ATTGCCCCCTTCTGT[A/G]AGCTCCAAGTTACTT | 317 |
rs754755261 | snp | C/G | 3.29484e-05 | 0.00405871 | intron-variant | APAF1 | GRCh38.p7 | 12:98659154 | CATTATTCTTTCCCT[C/G]ACTAGGTTGTTTCCC | 317 |
rs754789767 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699519 | GTGAAGTGTTGTTCG[C/T]GGTCTGCTGATGGTG | 317 |
rs754812968 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727038 | AATGGCAATATTAGT[A/G]TCTGTGTTAGGGTTG | 317 |
rs754839203 | snp | C/T | 6.60404e-05 | 0.00574594 | intron-variant | APAF1 | GRCh38.p7 | 12:98671491 | GGAAAAATGTCAGAT[C/T]GTGGCTCTGATTGTG | 317 |
rs754842939 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675131 | GTTTGACCAGTCCAT[A/G]TTCAAAGAATGCTTT | 317 |
rs754854448 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697193 | CTGTCTTAAGCTGGT[A/G]TAAGATAGGCTAATC | 317 |
rs754900925 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | APAF1 | GRCh38.p7 | 12:98725553 | AGGGTAGGCTGTTTG[C/T]TGACATGAGAGCACT | 317 |
rs754904382 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727198 | TCTCAAACGGTGAGC[C/T]TCTTCATTTGTGTGC | 317 |
rs754923668 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672877 | CTCCTGCCTCAGCCT[-/C]CCGAGTAGCTGGAAT | 317 |
rs754952556 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651666 | TATTTATTTATTTTT[G/T]TTTTTTTTTAAAGAG | 317 |
rs755110996 | in-del | -/TC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687473 | TAAAATATTTTGAGA[-/TC]TGTTTTAGTTTATTT | 317 |
rs755133056 | snp | C/T | 1.66907e-05 | 0.00288879 | intron-variant | APAF1 | GRCh38.p7 | 12:98648840 | CATTATACCTTCTAT[C/T]ACTTTGCTATCAAAA | 317 |
rs755141827 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716767 | TTCCAGTTTGCTTTC[C/T]CTTTTTGTAACACCC | 317 |
rs755160411 | snp | A/G | 4.94271e-05 | 0.00497102 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667522 | TTGCAGGATCTACAT[A/G]AGAAGATAATCACTC | 317 |
rs755193271 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702946 | GCAATTTGGTAGTTC[C/T]AGAGAGAAATAAAAA | 317 |
rs755205027 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666104 | AGGGCTTTAAGATAC[C/T]GTTTTTTTGTGTGTG | 317 |
rs755242803 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725430 | ATCTGGAGTTTTGAT[C/G]TCCTTTTGCCACTTC | 317 |
rs755258167 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650289 | GGAGTTCAAGACCAG[A/C]CTGGGCAACATGGTG | 317 |
rs755276894 | in-del | -/TTAG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708829 | GGTGTCCAGCAGACA[-/TTAG]TTAAATAAATATATA | 317 |
rs755284995 | snp | A/G | 3.2963e-05 | 0.00405961 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667636 | ATGGCCAGTGCCAAG[A/G]TGCACAAGGTAAGAT | 317 |
rs755288182 | in-del | -/GTGT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689497 | TGTGTGTGTGTGTGA[-/GTGT]GAGAGAGACACAGGG | 317 |
rs755373174 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715631 | ATGCCTAAAATCTGG[C/T]GTATATTTTAAACAC | 317 |
rs755387709 | in-del | -/TTAAG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692942 | AATGGTAGTTCTGTT[-/TTAAG]TTATTTGAGAAATCT | 317 |
rs755406259 | in-del | -/CCAGGCAGCCTCGCGTCCACTTACCAGG | 0.000123556 | 0.00785893 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644499 | CCACAGGAGGCCGGC[-/CCAGGCAGCCTCGCGTCCACTTACCAGG]CCAGGCCCAGGCACG | 317 |
rs755457660 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680888 | TGTGATTAGGAGTGT[C/T]GCTGCACAAACTTGG | 317 |
rs755461165 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657146 | CTTTTGAAATCTTGA[C/T]GTTGAGCATTCTCTT | 317 |
rs755473881 | snp | C/G/T | 3.38016e-05 | 0.00411095 | intron-variant | APAF1 | GRCh38.p7 | 12:98662597 | GTTTACTTTTTAGTA[C/G/T]CTTTATATTTAATTT | 317 |
rs755479492 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694931 | CCAGGCTGGAGTGCT[A/G]TGGCACCATCTCGGC | 317 |
rs755498688 | snp | C/T | 0.001023 | 0.0225932 | intron-variant | APAF1 | GRCh38.p7 | 12:98727166 | ATTGTGTATCATGTT[C/T]ATGTAGATATGGAAT | 317 |
rs755498862 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694170 | TCAAGCTATTAAAAT[C/G]CTAGAAGAAAACCTA | 317 |
rs755552913 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695795 | TCACCTTTATCAGAA[G/T]GTACTGGGTGCCAGC | 317 |
rs755593687 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644823 | TCACAGACTTGGCAC[C/T]GCCCAGAGCCCAGCC | 317 |
rs755627260 | in-del | -/TTATT | 9.91441e-05 | 0.00704004 | intron-variant | APAF1 | GRCh38.p7 | 12:98725366 | AATCAAGGCAGATGC[-/TTATT]TTGAGTGTTTATAGC | 317 |
rs755633684 | snp | C/T | 1.93156e-05 | 0.00310764 | intron-variant | APAF1 | GRCh38.p7 | 12:98683127 | TATTTGTAAATTTTT[C/T]CTCTTTTCTCTTTAG | 317 |
rs755639919 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673298 | CCAGCCTGGTCAACA[C/T]GGTGAAACCCATCTT | 317 |
rs755648185 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666236 | AAGAAGTTGAAGACA[C/T]ACTGCAGGAGTTTGT | 317 |
rs755681060 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698127 | ATTTAGACATGTATA[A/G]TCAAGTTGGATTGTG | 317 |
rs755683310 | snp | C/G | 1.69215e-05 | 0.00290869 | intron-variant | APAF1 | GRCh38.p7 | 12:98723613 | TAAAAGTGTCAACCT[C/G]CAAGTGTTTTTTTTT | 317 |
rs755686542 | snp | G/T | 1.64931e-05 | 0.00287163 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666315 | TTATTTACATGATCT[G/T]CAAGTAGATTTTCTT | 317 |
rs755708284 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682358 | GCGCCCGGCCTGATG[A/T]TTACTTTTTACTGAA | 317 |
rs755727824 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734029 | TAAGCCTTAATAAGA[C/T]TTTTCTAAGAAATGT | 317 |
rs755740436 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699526 | GTTGTTCGTGGTCTG[A/C]TGATGGTGCAAGGAT | 317 |
rs755740531 | snp | A/C/G | 3.2955e-05 | 0.00405914 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723728 | TTCTCACGATGCTAC[A/C/G]AAGTTTTCATCTACC | 317 |
rs755768948 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697028 | ACTCTGTTGGGGAAG[C/G]GTTCACATACCTGAT | 317 |
rs755789982 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659171 | CTAGGTTGTTTCCCA[C/G]GGGGAGTGCATTGGG | 317 |
rs755815651 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699427 | GGGATGCGACATCAG[-/C]AAATGAGAGGAAAAG | 317 |
rs755856547 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694032 | CAATGCGGGAGAGGA[-/CT]CTCTCTATTCAATAA | 317 |
rs755859380 | snp | A/T | 1.65151e-05 | 0.00287355 | intron-variant | APAF1 | GRCh38.p7 | 12:98703329 | AATAGCTTATCTCTT[A/T]AAGTATTTTACCTTC | 317 |
rs755864877 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659941 | GGAAATGTCTTAAGT[A/G]GGTGAGTTGGTGAGT | 317 |
rs755872148 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671639 | GGGTCTCTGTGAGCC[A/G]GAAACTTCAGAAGTT | 317 |
rs755880604 | snp | A/C | 1.87366e-05 | 0.00306071 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644631 | GTCTTCCCGCCCTCG[A/C]TCCGCTTCCCGGGCT | 317 |
rs755897055 | snp | G/T | 1.64917e-05 | 0.00287151 | intron-variant | APAF1 | GRCh38.p7 | 12:98671526 | TAAGAGATTTCAGTT[G/T]ATTTGTAGGATTGTG | 317 |
rs755923178 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723373 | TGCAATGATTATATT[C/G]AGACAGTCAAAAGCC | 317 |
rs755943177 | snp | A/G | 9.91785e-05 | 0.00704126 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708611 | AAAGAAAGTATGTAA[A/G]AACTCTGCTGTAATG | 317 |
rs755995180 | snp | A/T | 1.66283e-05 | 0.00288338 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665548 | ACTTCATTTTTTTTT[A/T]AAAGGCTCTCCCCTT | 317 |
rs756033039 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650111 | AGGCTGCCCCCATTC[A/G]TCAGTGTGTTCTCAT | 317 |
rs756075829 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687704 | CACTTTTGAAGGTCC[C/T]ATCTCTCAATACTTG | 317 |
rs756082336 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98665938 | AGAAATCCCTCTGCT[A/G]TTAGCTTCCATTAAG | 317 |
rs756120322 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665654 | AAGCAGTTTAAGAGA[A/G]TAAGGAAATCTTCGT | 317 |
rs756138030 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673785 | CCCCTAAGGAGTTCA[A/G]AATCTCGTAGTGAAG | 317 |
rs756138161 | snp | A/T | 1.65605e-05 | 0.0028775 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732486 | ACCAATCTTAAGAAA[A/T]TACACGTGTCCCCTG | 317 |
rs756158454 | in-del | -/ATTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669168 | CTCTAGTTATCGAAC[-/ATTT]ATTTAGGTTTTCAGT | 317 |
rs756164693 | snp | A/G | 1.65127e-05 | 0.00287334 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648728 | CTACATGAAGGATAT[A/G]AAGATCTTGCTGCCC | 317 |
rs756177170 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686812 | CAAATTCAGTCAATC[A/G]CTGCAGATTTTCACC | 317 |
rs756184861 | in-del | -/CT | 1.64768e-05 | 0.00287021 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715518 | CAGCCGATGAGAAGA[-/CT]CTTATTTCAAGTTCT | 317 |
rs756228371 | snp | C/T | 3.30376e-05 | 0.0040642 | intron-variant | APAF1 | GRCh38.p7 | 12:98667654 | CACAAGGTAAGATGA[C/T]CCATTTAAAAATTCT | 317 |
rs756263592 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671012 | CTGGATTGGATTAAA[A/G]CAAAAACAGAACTTG | 317 |
rs756270373 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730977 | GTGCATGAAGGGAAA[A/G]CTGATCTGAAGTATG | 317 |
rs756290188 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661061 | CTCCCCACCACACGC[C/T]GGGCTAATTTTTTGT | 317 |
rs756301921 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713182 | TTGTTCGTTAAACTA[A/G]CAATCATCTTATCCA | 317 |
rs756308809 | snp | G/T | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725551 | TCAGGGTAGGCTGTT[G/T]GCTGACATGAGAGCA | 317 |
rs756314920 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680619 | GCAGTGGCATGATCA[C/T]AGCTCACTGTAAACT | 317 |
rs756319379 | snp | A/G/T | 6.62365e-05 | 0.00575452 | synonymous-codon, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662456 | TTTTTTTTAAATTAG[A/G/T]TCTCTCTTGATCTTG | 317 |
rs756323821 | snp | A/T | 1.91316e-05 | 0.0030928 | intron-variant | APAF1 | GRCh38.p7 | 12:98699394 | TTTTTCTTTTTTATT[A/T]CTTTAATTCAAAGCT | 317 |
rs756390473 | snp | A/G | 1.74928e-05 | 0.00295738 | intron-variant | APAF1 | GRCh38.p7 | 12:98662604 | TTTTAGTACCTTTAT[A/G]TTTAATTTAATTACA | 317 |
rs756411622 | in-del | -/TTTG | 3.43731e-05 | 0.00414552 | intron-variant | APAF1 | GRCh38.p7 | 12:98662820 | AGGTATGGTTATTTA[-/TTTG]TTTATGAGGAGATTA | 317 |
rs756434679 | snp | A/G | 8.25089e-05 | 0.00642243 | intron-variant | APAF1 | GRCh38.p7 | 12:98727169 | GTGTATCATGTTTAT[A/G]TAGATATGGAATGTC | 317 |
rs756482718 | snp | A/C/G | 3.2955e-05 | 0.00405914 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648451 | TGGATCACATGATTA[A/C/G]TGATGGATTTTTAAC | 317 |
rs756501180 | snp | C/T | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729590 | GGACTGGGGACTCCT[C/T]TATATTGGGCTGATC | 317 |
rs756503344 | in-del | -/TTTATATG | 1.64741e-05 | 0.00286998 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671658 | CTTCAGAAGTTTATC[-/TTTATATG]AGCAAGCTAAGCTGC | 317 |
rs756525296 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721611 | TGGGTTCTTAAAATA[A/T]GAAAATTACTAATTC | 317 |
rs756555581 | snp | C/T | 1.65375e-05 | 0.0028755 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708627 | AACTCTGCTGTAATG[C/T]TAAAGCAAGAAGTAG | 317 |
rs756605547 | snp | A/T | 1.66482e-05 | 0.0028851 | intron-variant | APAF1 | GRCh38.p7 | 12:98648534 | CACACTTCCTTAAAA[A/T]TTTTTAGAATTTCAG | 317 |
rs756607971 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693879 | TAAGAAAGAATCTAT[A/G]GGAAGTAAATTTTTA | 317 |
rs756609234 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656246 | TATCCTAGAGATAAT[C/T]TTGGTTAACAATTCG | 317 |
rs756638702 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705789 | ATGAAGGTTAGATGA[C/T]AGTATTAGTGGAAAA | 317 |
rs756653729 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723739 | CTACCAAGTTTTCAT[C/T]TACCTCTGCTGACAA | 317 |
rs756655231 | snp | A/T | 1.69576e-05 | 0.00291179 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680362 | CATTCTCTACAGATG[A/T]CAGATTTATAGCAAC | 317 |
rs756690038 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706984 | TTATTATCTCTACCT[G/T]TCCATTTCTGCTGCC | 317 |
rs756729987 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658682 | TTTCACACCCCCCCA[A/G]GTGACATTTGACAAT | 317 |
rs756772271 | snp | C/T | 1.65075e-05 | 0.00287289 | intron-variant | APAF1 | GRCh38.p7 | 12:98703341 | CTTAAAGTATTTTAC[C/T]TTCATAGGTATCTCT | 317 |
rs756839017 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698529 | GTTGCAAGTAGAAAA[C/G]TTTTGGTTTTGGCCA | 317 |
rs756839291 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659299 | ACTTAATATTGAAGA[A/G]GCTAAAGACCGTCTC | 317 |
rs756840957 | snp | C/T | 2.82004e-05 | 0.00375492 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644567 | CAGCAGGCTCAGGCA[C/T]GTTCGGGGGTCTGCC | 317 |
rs756846991 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696031 | TTCTCCATTTTCCTT[C/T]GCCTTGTGGATTATG | 317 |
rs756858621 | in-del | -/GA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689442 | TGTGAGGGTGAGAGA[-/GA]GAGAGAGAGAGAGAG | 317 |
rs756868583 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671687 | GCAGGCCAAGCAGGA[A/G]GTCGATAATGGAATG | 317 |
rs756886354 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657254 | CAGAATATCCTCTCT[A/C]TTCATACTATCAGTC | 317 |
rs756898847 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676398 | ATTTTTAGTAGAGAT[-/G]GGGTTTCACCATGTT | 317 |
rs756914447 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703442 | CACCATCCAGTACTG[C/T]GACTTCTCCCCACAA | 317 |
rs756946634 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667100 | GGGAGATTCTCTGTA[-/TA]TATATATATGTATTT | 317 |
rs756953954 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663856 | TAGAGACGGGGTTTC[A/G]CCATGTTGGTCAGGC | 317 |
rs756959332 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674668 | ACTGCCTGGGTTTGA[A/G]TCCCAGCTCTGCTAT | 317 |
rs756965747 | snp | G/T | 1.82384e-05 | 0.00301974 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644643 | TCGCTCCGCTTCCCG[G/T]GCTCCGCAGCAGGGG | 317 |
rs757009936 | snp | A/C | 6.68349e-05 | 0.0057804 | intron-variant | APAF1 | GRCh38.p7 | 12:98671768 | GTGCGCTAACTATAT[A/C]ATTATTTTTCAGGTG | 317 |
rs757046622 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665668 | AATAAGGAAATCTTC[A/G]TCTTATGATTATGAG | 317 |
rs757066467 | snp | A/G | 1.89073e-05 | 0.00307462 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735515 | AAGCTAAATACATCA[A/G]CCTTTCTATTTAGGC | 317 |
rs757087470 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722089 | TGCGTCTCCTATGCT[C/G]TAGTCAGATGGACTC | 317 |
rs757169069 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664059 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 317 |
rs757171141 | snp | A/G | 1.65847e-05 | 0.0028796 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665788 | CGTTAAGGTGCCTAC[A/G]AAGGTAATGGGATCA | 317 |
rs757175459 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721632 | TTACTAATTCATTCT[C/G]TTTAGAATTACTCTC | 317 |
rs757184252 | snp | A/G | 3.35115e-05 | 0.00409324 | intron-variant | APAF1 | GRCh38.p7 | 12:98712470 | AGAATCTTTCTGTAC[A/G]GAATTAAATAAAACT | 317 |
rs757186699 | in-del | -/T | 1.64731e-05 | 0.00286989 | intron-variant | APAF1 | GRCh38.p7 | 12:98725571 | ACATGAGAGCACTGC[-/T]CTTCTTGTAGCTTGG | 317 |
rs757220580 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699682 | CTAGCTGTGTGATTT[G/T]GGGCAGTCTTCCTAA | 317 |
rs757237121 | snp | A/C/T | 8.23953e-05 | 0.00641807 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715507 | CATCCAGTTCACAGC[A/C/T]GATGAGAAGACTCTT | 317 |
rs757252142 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648283 | TCTTTTCATATTTTT[A/G]TTGGCCTGACAAATA | 317 |
rs757273980 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701284 | ATGGACACTTGGTTT[A/G]TTTCCACCTTTTGGC | 317 |
rs757281043 | snp | A/C | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729464 | CTAATGCCACCACTG[A/C]TCTCTCAGGAGACAA | 317 |
rs757316084 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709336 | CACCCAACAAAGAGT[A/G]GGACACGTGAGAGGA | 317 |
rs757331016 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713146 | TTATACTAAATAAAT[C/T]TTTCTGTGATCTATT | 317 |
rs757360181 | snp | A/G | 1.74848e-05 | 0.0029567 | intron-variant | APAF1 | GRCh38.p7 | 12:98662617 | ATATTTAATTTAATT[A/G]CATTTAAATATGTGA | 317 |
rs757373827 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671039 | CTTGTAGGCCCTGCT[C/T]ATCTGATTCATGAAT | 317 |
rs757428659 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671130 | CTAAAAAGGAATCTC[A/T]TTTTTTTTTACATTT | 317 |
rs757459967 | snp | A/G | 3.32508e-05 | 0.00407729 | intron-variant | APAF1 | GRCh38.p7 | 12:98648575 | GGTCTCCACTACTTT[A/G]TGTTGCATACATATT | 317 |
rs757485552 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678085 | ACATGATGAAATTAG[C/T]TAAAACTTGTATTTA | 317 |
rs757493517 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727270 | TGACTGACCTTTGCT[A/T]TTCTCCAGATGGCAA | 317 |
rs757495661 | snp | A/T | 8.29841e-05 | 0.0064409 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708655 | TAGATGTTGTGTTTC[A/T]AGAAAATGAAGTGAT | 317 |
rs757500870 | snp | C/G | 1.68088e-05 | 0.00289899 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680385 | ATAGCAACCTGCTCA[C/G]TGGATAAAAAAGTGA | 317 |
rs757541629 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656136 | TTTCACCATGTTGCT[C/T]AGGCTGGTCTCGAAA | 317 |
rs757551566 | snp | C/G | 3.72745e-05 | 0.00431693 | intron-variant | APAF1 | GRCh38.p7 | 12:98708743 | TGGAAAATTGTTTTG[C/G]TTGAATTTTCTATTC | 317 |
rs757575463 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729073 | CTAAAGTTTAGAAGG[A/G]GTCTGGGACATGCTT | 317 |
rs757661181 | snp | A/C | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648704 | TACGTATCATTCTAC[A/C]ATGCTCTACTACATG | 317 |
rs757675000 | snp | A/G/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683228 | ATTTCACCAACAGTA[A/G/T]TCATCATCTTCTCTT | 317 |
rs757689723 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705524 | AGTCACTGGGCCTAT[G/T]ATGAGGTACTTGTTT | 317 |
rs757690871 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719434 | GGCTCACTGCAGCCT[C/G]CGCCTCCTGGGTTCA | 317 |
rs757702293 | snp | A/T | 1.65679e-05 | 0.00287814 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683152 | CTTTAGATTTGGAAT[A/T]CTATGACTGGGGAAC | 317 |
rs757730495 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668702 | AAACCCCAGTGGAAA[A/G]AACGGAGTCCATGAA | 317 |
rs757755298 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667287 | TTTTTTATTTTTTGT[A/T]AAAAAATTAAATATA | 317 |
rs757781136 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703450 | AGTACTGTGACTTCT[C/T]CCCACAAAACCATTT | 317 |
rs757791240 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718324 | TGAAACCTCCACCTC[C/T]GAGGTTCAAGTGATT | 317 |
rs757833080 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685359 | TTTTTTTTTTTGAGA[C/T]GGCATCTTGCTCTGT | 317 |
rs757855515 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725129 | CTCACATTCAGGTCT[C/G]CTTCACTCCACAGAC | 317 |
rs757924189 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696795 | CCACTGCACCCTGCC[-/G]GGGAGTAATCAGTCT | 317 |
rs757928400 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720209 | TATTCTCAGCTAGGG[A/G]GAAGAATAATTTCTA | 317 |
rs757953012 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686125 | CCATATTCTCAAAAC[A/T]TGCATTTCTATCATG | 317 |
rs757979558 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678555 | AACCACAGCTGCAGG[C/T]TCGGGCCTCCGGCTC | 317 |
rs757980121 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707128 | TGCAGTCATGTCATT[G/T]TTGCTCAAAAATAAG | 317 |
rs757986082 | snp | G/T | 6.58957e-05 | 0.00573964 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706550 | AAGTTGGGTTCATGG[G/T]GTGATGTTTTCTCCT | 317 |
rs758005958 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721934 | TCATGTGCATACCTG[C/T]AGTTGTGGCTGCTTT | 317 |
rs758021604 | snp | A/T | 1.65086e-05 | 0.00287298 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665676 | AATCTTCGTCTTATG[A/T]TTATGAGGCTCTAGA | 317 |
rs758032954 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651218 | TTATTATAGTAGATC[A/T]GTACTAGGCTGAGCT | 317 |
rs758039577 | snp | A/T | 4.94474e-05 | 0.00497205 | intron-variant | APAF1 | GRCh38.p7 | 12:98677557 | AACCTTACAGGTAAA[A/T]CACATCTCTTGAGAA | 317 |
rs758052483 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694452 | GTTTCTGGATTAAAA[-/T]TTTTTTTCCTCTCCT | 317 |
rs758063841 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648206 | CATTTAAAAATTTTT[G/T]CCAAGGAAAAAAAAT | 317 |
rs758073552 | snp | A/G | 1.67178e-05 | 0.00289113 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735616 | GTTCCTGCCCGGTAT[A/G]GCTGGCATGAAGAAG | 317 |
rs758090671 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687147 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 317 |
rs758115685 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660750 | CTTGGGAATGTTATA[-/G]TATACTGAGTGAGAG | 317 |
rs758129366 | in-del | -/A | 4.97876e-05 | 0.00498912 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677429 | CCTGTATTTAGAAAC[-/A]AAAAAAACATCACGA | 317 |
rs758148327 | snp | G/T | 1.66294e-05 | 0.00288347 | intron-variant | APAF1 | GRCh38.p7 | 12:98665808 | TAATGGGATCAATGA[G/T]CCTCATCATTGGGTA | 317 |
rs758151691 | snp | G/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646677 | ATTGAATGAATGAAT[G/T]GATAAACCCGTTTAG | 317 |
rs758155975 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715513 | GTTCACAGCCGATGA[A/G]AAGACTCTTATTTCA | 317 |
rs758201221 | snp | A/G | 3.30316e-05 | 0.00406383 | intron-variant | APAF1 | GRCh38.p7 | 12:98649478 | TGCTTGTTTTGTTTT[A/G]GATTTTAGTAAGGAC | 317 |
rs758227409 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660265 | GTGGGAGGATCACTT[A/G]AGCCTATGAGATTGA | 317 |
rs758268458 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683774 | CAAGGGTCACAAGTT[C/T]AGTTATATGGAAGTG | 317 |
rs758307834 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677868 | AGCACAGGGAATAGG[C/G]CTGTGATTAAAAAAC | 317 |
rs758311077 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729236 | GATGATACTCTATAT[C/T]AGCGGTCCCCAGCCT | 317 |
rs758339778 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695911 | TGTGGGGTGATTGGG[-/C]TGCTTGGATTTCTCC | 317 |
rs758365663 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711685 | AGGTCACATGTTTTA[A/G]ATGAGTGATAAGGCA | 317 |
rs758392274 | snp | C/T | 5.01375e-05 | 0.00500662 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699418 | CAAAGCTTTGGGATG[C/T]GACATCAGCAAATGA | 317 |
rs758417207 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712806 | GGCATGGGAGCTTTT[A/G]TGCCTGGCTATTGTA | 317 |
rs758439891 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669933 | CCTCCCCTCTTCCTG[-/C]CCTTGCCCTTTCTTT | 317 |
rs758448810 | snp | A/G | 1.65403e-05 | 0.00287574 | intron-variant | APAF1 | GRCh38.p7 | 12:98727323 | TATATTAAGGTAAGA[A/G]TTCCCCAAGAACTGT | 317 |
rs758454889 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671620 | TTCCTAATATTGTAC[A/G]ACTGGGTCTCTGTGA | 317 |
rs758478742 | snp | G/T | 1.64961e-05 | 0.00287189 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732432 | CAGTGGTGGAACGTT[G/T]TCACTGGGGAATCCT | 317 |
rs758538954 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692231 | GGGAGTACAGGCGCC[C/T]GCTGCCATGCCCGGC | 317 |
rs758539393 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676972 | TTTAAAGTACATCAT[A/C]ATAATGGTGGGTGTT | 317 |
rs758543506 | snp | A/G | 1.65002e-05 | 0.00287225 | intron-variant | APAF1 | GRCh38.p7 | 12:98712284 | AAAAACTGCTCTTAC[A/G]GCCTAATAACTGATT | 317 |
rs758566308 | snp | C/T | 0.000250186 | 0.0111817 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665528 | AGGATGGTATTAGCA[C/T]AGTGACTTCATTTTT | 317 |
rs758593996 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727403 | TGTTTCTCAGTTGGG[C/T]CTTTTACAACCCAGC | 317 |
rs758597432 | snp | C/G | 1.64969e-05 | 0.00287196 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683164 | AATTCTATGACTGGG[C/G]AACTAGTACACACCT | 317 |
rs758599595 | snp | C/T | 3.30017e-05 | 0.00406199 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712381 | AGTTAGCTGCTGTTG[C/T]TTAAGTCCACATCTT | 317 |
rs758608665 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704068 | ACCCAGTGAAGTGCT[A/G]TATTAGTTTTTTCAT | 317 |
rs758632038 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690259 | AACTCTTTCTGGGTA[G/T]AATTCTACTTTGTAG | 317 |
rs758689138 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716956 | CTGTAACCTCTGCCT[C/T]CTGGGTTCAGGCAAT | 317 |
rs758689255 | in-del | -/ATGT | 1.65214e-05 | 0.0028741 | intron-variant | APAF1 | GRCh38.p7 | 12:98727160 | AATGAATTGTGTATC[-/ATGT]ATGTTTATGTAGATA | 317 |
rs758691720 | snp | A/T | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648715 | CTACAATGCTCTACT[A/T]CATGAAGGATATAAA | 317 |
rs758722635 | snp | C/T | 4.94662e-05 | 0.00497299 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715483 | TCAGCACAAGAAAAC[C/T]GTATGGCACATCCAG | 317 |
rs758724237 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683264 | CTGGGTCAAGTGACT[A/G]CTTCCTCAAAGTAAG | 317 |
rs758767392 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667241 | GTTGGGTCTGCAGGC[A/G]TATGCCACCACACCT | 317 |
rs758799249 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696830 | ACTTAAAATGTATTT[A/T]TTGAATACTTAGTGT | 317 |
rs758814204 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703033 | CATTTATGAGTATTC[A/G]TTTTCTCTTTTGAAT | 317 |
rs758831215 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733859 | AGTTGTCAGTATCTG[A/C]GTTGGACACTATTCC | 317 |
rs758870589 | snp | A/C | 1.74937e-05 | 0.00295745 | intron-variant | APAF1 | GRCh38.p7 | 12:98662428 | AAGATAAGTGTCATT[A/C]GTGATTAATATTTTT | 317 |
rs758874019 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723753 | TCTACCTCTGCTGAC[A/G]AGACTGCAAAGGTAG | 317 |
rs758901927 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667621 | TTTCTGGCCTATCAC[A/G]TGGCCAGTGCCAAGA | 317 |
rs758919119 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732757 | CATACCTTTAATCTT[A/G]TTTTTCATGATCATC | 317 |
rs758924156 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659306 | ATTGAAGAGGCTAAA[G/T]ACCGTCTCCGCATTC | 317 |
rs758991431 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654817 | TAAAGTAGTATTTTC[-/TT]TTTTTTTTTTTTTTT | 317 |
rs758992275 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660498 | TTAATTCAGCAAATA[C/T]TTACCATTATAATTA | 317 |
rs758999715 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | APAF1 | GRCh38.p7 | 12:98725396 | ATAGCATTGCTAAAC[A/G]ATCCTAATTGCCTTC | 317 |
rs759011965 | snp | C/G | 1.79059e-05 | 0.00299209 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644658 | GGCTCCGCAGCAGGG[C/G]CTCCCTTGGGCCCCG | 317 |
rs759065118 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648005 | GTGGATATTTTTACA[C/T]ATGTATTTGAATGTC | 317 |
rs759065424 | snp | A/G | 1.73519e-05 | 0.00294545 | intron-variant | APAF1 | GRCh38.p7 | 12:98662831 | TTTATTTGTTTATGA[A/G]GAGATTATAGGGAGT | 317 |
rs759075433 | snp | C/T | 1.65315e-05 | 0.00287498 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708604 | GGGAGACAAAGAAAG[C/T]ATGTAAGAACTCTGC | 317 |
rs759118081 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649282 | CTTCCATTTTCTTTA[G/T]TCATCTTGAAGGATA | 317 |
rs759119224 | snp | A/C | 1.66222e-05 | 0.00288285 | intron-variant | APAF1 | GRCh38.p7 | 12:98648526 | AAGCAGTCCACACTT[A/C]CTTAAAAATTTTTAG | 317 |
rs759138022 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687361 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 317 |
rs759154322 | snp | A/T | 1.64871e-05 | 0.00287111 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666302 | AGTCGTTTCGTTATT[A/T]TTTACATGATCTTCA | 317 |
rs759164816 | in-del | -/AAAG | 1.65296e-05 | 0.00287481 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723663 | ATTATTACTGGAAAT[-/AAAG]AAAAAGACTTTGTCT | 317 |
rs759182999 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677754 | TCTAAACTTACAGGT[A/G]GTAAGGAAGTGCCCT | 317 |
rs759184606 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712639 | TTCCCACTTAAGCCT[C/T]CTGAGTAGCTGGGAC | 317 |
rs759213602 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678589 | AGAGCAGGCAGGACC[C/T]CTTCCCCCTGGTGCA | 317 |
rs759227465 | snp | C/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730213 | TTATTCAGTTATTAG[C/G]AGATCCTGAGAAATG | 317 |
rs759254163 | snp | A/G | 0.000557919 | 0.0166928 | intron-variant | APAF1 | GRCh38.p7 | 12:98683104 | GTTCTCCCTTTGAAA[A/G]TAATGGATATTTGTA | 317 |
rs759256347 | snp | C/T | 0.000280392 | 0.0118371 | intron-variant | APAF1 | GRCh38.p7 | 12:98712315 | TTGCCTCATTTTTCA[C/T]TAGCTCATTAATGGA | 317 |
rs759267236 | in-del | -/AAGATTCCCTTTGTTTTCAGAAAATATTAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677992 | TAAAGAATTTCCTTT[lengthTooLong]TGAGTACTTTTCTTT | 317 |
rs759299029 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663607 | TCTATCAACTCTTAA[A/T]ATTATTTCTTTCATT | 317 |
rs759307185 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683196 | TGATGAGCACTCAGA[A/G]CAAGTCAATTGCTGC | 317 |
rs759307574 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693241 | TTTAATGTTATTGAT[A/G]TACAGAAATGCTGCT | 317 |
rs759340274 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675180 | TTTTTGGTGTTTACT[A/G]TAGAAAGGTTTAGGT | 317 |
rs759382270 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723717 | TCTTGTGACATTTCT[C/G]ACGATGCTACCAAGT | 317 |
rs759403755 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | APAF1 | GRCh38.p7 | 12:98667464 | AGTTACTGTGATGCT[C/T]AGGTTATAAAATTGT | 317 |
rs759412251 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691937 | TTTTTCAGGTATGTC[A/T]TCTGCAACCTTCATT | 317 |
rs759423254 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719534 | TTTTTTTTTTTTTTT[-/A]GTAGAGTTGGGGTTT | 317 |
rs759433559 | snp | A/T | 4.94613e-05 | 0.00497275 | intron-variant | APAF1 | GRCh38.p7 | 12:98723799 | CCATGCATAAAACTT[A/T]GGTAGTGGTTATGTA | 317 |
rs759437111 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656062 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC | 317 |
rs759441502 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705196 | TGTCACTTCTAAAGT[A/C]CTTACCCTCTGCCAT | 317 |
rs759450443 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728950 | GACTGTGTTGAATGT[C/T]CAGTGTGTGCTAAGC | 317 |
rs759455114 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659256 | GCACACGGTTGGATC[A/G]GGATGAGAGTTTTTC | 317 |
rs759485502 | snp | A/G | 1.67911e-05 | 0.00289746 | intron-variant | APAF1 | GRCh38.p7 | 12:98699609 | CAGTCTGATTTAAAG[A/G]AAGTTAAAACTTCTG | 317 |
rs759494539 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705979 | TCCTTCCCTGCATAT[A/G]TAAACTATTTTCTGT | 317 |
rs759599867 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668228 | ATTATAGCTTGCATA[A/G]TTATTTTTGTTTTTA | 317 |
rs759621299 | snp | A/G | 0.000178047 | 0.00943354 | intron-variant | APAF1 | GRCh38.p7 | 12:98680256 | TTTATTATAAAAAAT[A/G]TTTTATTGTTACTTG | 317 |
rs759653800 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697517 | CTTCAAACTCGGACA[C/G]TTTTTAAAAAGTCAT | 317 |
rs759683805 | in-del | -/GACC | 4.94752e-05 | 0.00497344 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699476 | TTCCTAAATTTGGAG[-/GACC]GACCCTCAAGAGGAT | 317 |
rs759745837 | snp | A/T | 1.68354e-05 | 0.00290128 | downstream-variant-500B, stop-gained | APAF1, ANKS1B | GRCh38.p7 | 12:98735568 | AATTCTATCAAAATT[A/T]TCTGAGTGCCTCCTC | 317 |
rs759773140 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | APAF1 | GRCh38.p7 | 12:98715602 | GCTGATTCTAGCAAA[A/G]GAACACTATGATTAT | 317 |
rs759795819 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant | APAF1 | GRCh38.p7 | 12:98666168 | CTTTTGTGGCATATT[A/G]AATACTTACAACAAT | 317 |
rs759806743 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681849 | TTAAAGAACTTTAAA[A/C]TAAGATAAACTCTCT | 317 |
rs759810056 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734678 | TTAAGGAGGTTTTTT[A/G]TTTTTAAATGGTGGG | 317 |
rs759825309 | snp | A/G | 1.66824e-05 | 0.00288806 | intron-variant | APAF1 | GRCh38.p7 | 12:98649454 | TTATTCCAAAGTTCT[A/G]TTCATTCATGCTTGT | 317 |
rs759884217 | snp | C/T | 1.64779e-05 | 0.00287031 | stop-gained, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649567 | CTGGTGAATGCAATT[C/T]AGCAGAAGCTCTCCA | 317 |
rs759895384 | snp | C/T | 3.29908e-05 | 0.00406132 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98670983 | TAAAGGAACTTTGTG[C/T]TTTAATGTTTTCCCT | 317 |
rs759933798 | snp | A/T | 1.65425e-05 | 0.00287593 | intron-variant | APAF1 | GRCh38.p7 | 12:98727152 | AACTCTGTTAATGAA[A/T]TGTGTATCATGTTTA | 317 |
rs759943994 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674549 | TCATAGGATTTGTCA[C/T]ACTTTATAGTGATTA | 317 |
rs760041627 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696685 | TTTGTTTTTAGAGAC[A/G]GGGTTTCACCATGTT | 317 |
rs760061998 | snp | G/T | 0.000153104 | 0.00874807 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644482 | CCCAAACAGCAGGGG[G/T]CCCACAGGAGGCCGG | 317 |
rs760067486 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689443 | GTGAGGGTGAGAGAG[A/T]GAGAGAGAGAGAGAG | 317 |
rs760089515 | snp | A/G | 1.66771e-05 | 0.00288761 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662714 | AGAGTTCCTTAGGAA[A/G]GGAAAAAGGACTTGA | 317 |
rs760104591 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709293 | TTAGGGATCCAAACA[A/G]CACTACTCTAGTCTG | 317 |
rs760122718 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675746 | TGGTATCTGTAGTGG[A/G]TCCTAGAACCAATCC | 317 |
rs760180511 | in-del | -/AT | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665256 | TGCTTAGACTGGCGC[-/AT]ATATATATATATATA | 317 |
rs760194245 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712330 | TTAGCTCATTAATGG[A/G]AGAACAGGTCAGATT | 317 |
rs760203216 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661485 | TTTTTATTTTTATTT[G/T]TATTTTTTTAGATGG | 317 |
rs760217344 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705097 | GATCTTGAACCTTAT[G/T]TGTAGATCCTCAAAG | 317 |
rs760244628 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728704 | CTCCAGCCTGGGCAA[C/G]AGAGCGAGACTATCT | 317 |
rs760249414 | snp | A/C | 6.58903e-05 | 0.00573941 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683211 | GCAAGTCAATTGCTG[A/C]CATTTCACCAACAGT | 317 |
rs760266444 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676116 | TTGACATATTTACTT[A/G]TACTCAAAGTGACAG | 317 |
rs760324432 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98711225 | GACAAATTTAGTGTC[C/T]TCATGCTTGTATTTC | 317 |
rs760325358 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726482 | TGCAGAAGACTAGGA[G/T]AGTATACAGTTTGCA | 317 |
rs760337840 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683956 | ATTGTATCTTTTTTT[-/C]CTCTTAAGTGGATAA | 317 |
rs760356021 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691350 | TTTCCACAGCTTACA[A/G]ATGTTCTTGGGCCTT | 317 |
rs760384892 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676312 | CCTCCAGGGTTCAAG[C/T]GATTCTCATGCCTCA | 317 |
rs760410639 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652540 | TATTTTCCATTGGGG[A/T]TTCCAATTTTTTTTT | 317 |
rs760417324 | snp | C/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735231 | TTTCTAAAGCATTTT[C/G]CCTTGCTGTATTTTT | 317 |
rs760440119 | snp | G/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659281 | TTTTTCCCAGAGGCT[G/T]CCACTTAATATTGAA | 317 |
rs760458871 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689819 | TGGTTCTGAGTACAT[A/G]TATCTATCTATATCT | 317 |
rs760473774 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703429 | CGGGCCATCACAGCA[C/T]CATCCAGTACTGTGA | 317 |
rs760531403 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725475 | CACAACGGCTGTGTG[C/T]GCTGCTCTGCCTTCT | 317 |
rs760538944 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703819 | TCTCTTATCCAGTAT[A/G]GATATGTGGCATTTC | 317 |
rs760558746 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652322 | GTACATTTCCCCCAG[A/G]TGAGTATGGGGACTC | 317 |
rs760561694 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718033 | AACAGGAAGTATTAA[C/T]AGATGTTGGATCTCA | 317 |
rs760566673 | snp | C/G | 1.65007e-05 | 0.00287229 | intron-variant | APAF1 | GRCh38.p7 | 12:98659378 | GTTGGTGTGTCAGGT[C/G]CCATGTCCCAATAAG | 317 |
rs760587585 | snp | A/G | 1.64784e-05 | 0.00287035 | utr-variant-5-prime, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648353 | AGAGAGAAAGATCTG[A/G]GGGAAGATGGATGCA | 317 |
rs760590789 | snp | A/C | 1.77231e-05 | 0.00297678 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644718 | TCTGGAGACCCTAGG[A/C]CGACAAGCCCAGGGC | 317 |
rs760646025 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666963 | AGTGCTGAGATTGTA[A/G]GTATGAGCCACTATT | 317 |
rs760691992 | snp | A/C | 3.29701e-05 | 0.00406005 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649597 | AAATTGAAAGGTGAA[A/C]CAGGATGGGTCACCA | 317 |
rs760738827 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681688 | CTCGTGGCTTAACCA[A/G]CAGTTAATTCACTCT | 317 |
rs760739557 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732196 | CCAGCACAACTCAAC[A/G]GTTGGAGTTGGGTGT | 317 |
rs760754914 | in-del | -/TTTATGTTTGTGT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678034 | TAATGAGTACTTTTC[-/TTTATGTTTGTGT]TCTGCCTTTTGATTT | 317 |
rs760784833 | in-del | -/T/TT/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667765 | TTGCTTTCCATTTGA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 317 |
rs760792555 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733322 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 317 |
rs760801576 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658154 | ATGCTACTGTTTACC[A/G]TATTTTACACATAGG | 317 |
rs760834151 | snp | A/C/G/T | 0.000718245 | 0.0189385 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708680 | AGTGATGGTCCTTGC[A/C/G/T]GTTGACCATATAAGA | 317 |
rs760882230 | snp | G/T | 1.64893e-05 | 0.0028713 | intron-variant | APAF1 | GRCh38.p7 | 12:98659114 | AACCATTTAAAGGAG[G/T]ACTCCTGTTGAAAGG | 317 |
rs760924177 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655906 | CTCCTGCCCCAGCCT[-/C]CCGAGTAGCTGGGAT | 317 |
rs760954769 | snp | C/G | 3.29549e-05 | 0.00405911 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671592 | AATGGACACCTTCTT[C/G]GACGACAGCCATTTC | 317 |
rs760972323 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674253 | TTCCTTGACTTCCCA[A/G]AGTTCTTGGATTACA | 317 |
rs760996447 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696604 | CTGAACCCTATTTCT[C/T]TCAGCAACACTATTG | 317 |
rs761053474 | snp | C/T | 1.79686e-05 | 0.00299733 | intron-variant | APAF1 | GRCh38.p7 | 12:98708727 | TTTTTTAGAAAACAA[C/T]TGGAAAATTGTTTTG | 317 |
rs761076388 | snp | A/G | 3.32563e-05 | 0.00407763 | intron-variant | APAF1 | GRCh38.p7 | 12:98699586 | TAAGTACTTTAAAAA[A/G]CCAACTTCAGTCTGA | 317 |
rs761085092 | snp | C/G | 8.23689e-05 | 0.00641698 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727256 | CCATGGAGGCTGGGT[C/G]ACTGACCTTTGCTTT | 317 |
rs761157351 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688640 | CACACCTGGCGAAAT[-/TT]TTTTTTTTTTTTTTT | 317 |
rs761176384 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708086 | TGAGTAGCTGGGACC[A/G]CAGGTGCACACCACC | 317 |
rs761197564 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687945 | GTCTCCCAAGTAGAT[A/C]GGAGTACAGGCGCCT | 317 |
rs761201338 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672655 | GGAAAGGATAGCTAT[G/T]AATACCATCTTTTTA | 317 |
rs761221845 | in-del | -/A | 1.64749e-05 | 0.00287005 | intron-variant, frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703468 | ACAAAACCATTTGGC[-/A]AGTGGTTGCTTTGTC | 317 |
rs761233274 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680760 | AAAATGCCTAGGTTG[A/T]TCACCTCAGGATTAA | 317 |
rs761246902 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722973 | AAAACAAATTTTATT[G/T]AGGAGGAAAAGTATT | 317 |
rs761325999 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721733 | GAATGAGCATTCTGA[-/G]GGCAGAAGATGAGAG | 317 |
rs761349739 | snp | A/G | 6.58892e-05 | 0.00573936 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725499 | GCCTTCTCTGTGGAC[A/G]GTACCCTGCTGGCAA | 317 |
rs761359651 | snp | G/T | 1.7067e-05 | 0.00292117 | intron-variant | APAF1 | GRCh38.p7 | 12:98670925 | TGTTATACCTAAAAT[G/T]TTTTGATCTCTAACA | 317 |
rs761360731 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726462 | CTCCAGGAACAGGTA[C/T]ATAGTGCAGAAGACT | 317 |
rs761477565 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706521 | TCAAAGGTGGCTGAT[C/T]GCAGAGGACATTTAA | 317 |
rs761504755 | in-del | -/TATATATATAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653692 | AAAAAAAAAAAAAAA[-/TATATATATAT]TATATATATATATAT | 317 |
rs761524176 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703666 | TATTAAACCACATAG[A/C]CAGCTTTATTATTTT | 317 |
rs761528124 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688536 | GAGTGCAGTGGTACC[A/G]TCATGGCTCACTGCA | 317 |
rs761550622 | snp | A/G | 0.000141348 | 0.00840559 | intron-variant | APAF1 | GRCh38.p7 | 12:98662416 | AAAAGGAAGCTTAAG[A/G]TAAGTGTCATTAGTG | 317 |
rs761581262 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689663 | ATGGGGCCTCCCTGT[A/G]TTACCCAGGCTGGTC | 317 |
rs761605795 | snp | A/G | 1.77558e-05 | 0.00297953 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644725 | ACCCTAGGACGACAA[A/G]CCCAGGGCAGCTTCT | 317 |
rs761612379 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677526 | GTCAGAGAATAGCTT[C/T]TTGTGGAGCTGATAA | 317 |
rs761637675 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696473 | CACCTCCTATCAAGC[C/G]CTACTTCCCAACACT | 317 |
rs761667072 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656073 | CAGGCATGAGCCACC[A/G]CGCCCGGCCTTGCCT | 317 |
rs761691120 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681483 | GGGTTATCACTGATA[C/T]ATGGAAGACAGACCT | 317 |
rs761699492 | in-del | -/AA | 3.29451e-05 | 0.00405851 | frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659202 | TTTCAGTTGGGAAAC[-/AA]GACAAATCTGGGCTT | 317 |
rs761720699 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680188 | TTTTGCAAAATGACA[A/G]TGATTAAACTCACTT | 317 |
rs761725300 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717910 | TTGTTGTGAGTATCT[G/T]CAGGTCTTTTGTCTT | 317 |
rs761725653 | in-del | -/CTC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684478 | CCTCTCTTCTTCTGT[-/CTC]CTCCTCCTCCTCCCT | 317 |
rs761730145 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648381 | GCAAAAGCTCGAAAT[C/T]GTTTGCTTCAACATA | 317 |
rs761736799 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680281 | TACTTGTGCAGGTGT[C/T]CAAAGCTGAAACAGG | 317 |
rs761758965 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702455 | TATATTGTATCAATA[C/T]ATGTAGTAAATAAAA | 317 |
rs761762347 | snp | C/G | 1.64808e-05 | 0.00287057 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723689 | CTTTGTCTGTCACCA[C/G]GGTACAGTACTTTCT | 317 |
rs761771600 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98665886 | GAACCTTGGAAGGAT[A/G]AGACCCAGGGGACTG | 317 |
rs761777763 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant | APAF1 | GRCh38.p7 | 12:98666178 | ATATTAAATACTTAC[A/G]ACAATTCCTAGGTGT | 317 |
rs761786811 | snp | C/T | 3.33478e-05 | 0.00408323 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735604 | GTCTCTCTGATGGTT[C/T]CTGCCCGGTATGGCT | 317 |
rs761865771 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727216 | TTCATTTGTGTGCTC[C/T]GCTTTCAGAAGAAGG | 317 |
rs761898037 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652446 | TTTCTCTGGTAACTC[A/G]AGTTTGAACATTTCT | 317 |
rs761899526 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706877 | AATACTGCATTTGAT[C/T]CCTCAGAAAAATTTT | 317 |
rs761903065 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657886 | AATGAATGAACATAC[A/C]GAGAACTCTTAGAAT | 317 |
rs761964469 | snp | C/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643469 | CTTATTAAAATGAAA[C/T]GGGCTATTCCCTCCT | 317 |
rs761965932 | snp | A/G | 2.11155e-05 | 0.0032492 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644605 | CGCCTCCGCTGCTCC[A/G]GGCCACGGGGGTCTT | 317 |
rs761999940 | snp | A/G | 1.6696e-05 | 0.00288924 | intron-variant | APAF1 | GRCh38.p7 | 12:98699595 | TAAAAAGCCAACTTC[A/G]GTCTGATTTAAAGAA | 317 |
rs762019953 | in-del | -/AT | 8.30296e-05 | 0.00644266 | intron-variant | APAF1 | GRCh38.p7 | 12:98708539 | CTTTAAGATGAAGAC[-/AT]GTTATTTTAGAGATG | 317 |
rs762046476 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688740 | GCTGGGATTATAGGC[A/G]TGAGCCACCAAGCCT | 317 |
rs762070029 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668870 | TGAGTCTAGAATTCT[G/T]GGGAGAATTATAGAT | 317 |
rs762087633 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659801 | AGAAAGAACCATTGC[G/T]TTCCTGCTTTTCTCT | 317 |
rs762101149 | snp | C/G | 1.65397e-05 | 0.00287569 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732412 | GAATTTTATTTTTCT[C/G]TGAACAGTGGTGGAA | 317 |
rs762106922 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707924 | TGTGTTTAGTGATGT[A/G]GTTGATTTACGTTCT | 317 |
rs762122714 | snp | A/G | 4.94254e-05 | 0.00497094 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671610 | CGACAGCCATTTCCT[A/G]ATATTGTACAACTGG | 317 |
rs762135366 | snp | C/T | 1.76714e-05 | 0.00297244 | intron-variant | APAF1 | GRCh38.p7 | 12:98662851 | TTATAGGGAGTTATA[C/T]AATTTCCCTTTTGTT | 317 |
rs762174133 | snp | A/T | 1.64936e-05 | 0.00287168 | intron-variant | APAF1 | GRCh38.p7 | 12:98671730 | TGGATGTAAGTAGGT[A/T]AGGAGAGAAACCAAA | 317 |
rs762188284 | snp | C/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646808 | TTTGAAATAAAGTTG[C/T]TAGAAACGTCAAGTA | 317 |
rs762198187 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683232 | CACCAACAGTAGTCA[A/T]CATCTTCTCTTAGCC | 317 |
rs762222425 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646263 | ACATCGAATTTCATT[A/G]CTATAAATTAAGGAA | 317 |
rs762223867 | snp | G/T | 3.29891e-05 | 0.00406122 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712349 | ACAGGTCAGATTGAT[G/T]ATCTGACTGAAGCTC | 317 |
rs762226148 | snp | A/C | 1.73438e-05 | 0.00294476 | missense, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732526 | CATATGTGACTGTGG[A/C]TAATCTTGGTATTTT | 317 |
rs762242487 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656653 | TCTGTGAGCAGGAAA[-/CT]CTCTTGTATCATCAA | 317 |
rs762264513 | in-del | -/TTT | 0.000675139 | 0.0183607 | intron-variant | APAF1 | GRCh38.p7 | 12:98723620 | GTCAACCTCCAAGTG[-/TTT]TTTTTTTTTTTTTAA | 317 |
rs762300381 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688286 | TCTTTCTTTGGTCTT[A/C]AGATCAACCCATCTT | 317 |
rs762317028 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721374 | TTGAATCAGGCAAAG[C/G]TAGAATAGGCAGTGT | 317 |
rs762322831 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650801 | TTTTTAAGCCCCTAC[A/T]GCAAAGTTGATCACT | 317 |
rs762334389 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685438 | CCTCCCGGGTTCAAG[C/T]GATTTCCCTGCCTCA | 317 |
rs762349701 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735160 | GCTGCAAATTTCATG[A/G]CAGTTCATGCAGTCG | 317 |
rs762402964 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663477 | CCTTAGCCTCCTAAA[A/G]CACTGGGACTACAGG | 317 |
rs762430187 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647805 | GGCTGCATAATATTC[C/T]ATTTTATATACATAC | 317 |
rs762432240 | in-del | -/TTTTTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667265 | CACACCTGACTGATT[-/TTTTTTA]TTTTTTATTTTTTGT | 317 |
rs762442275 | snp | A/G | 3.51648e-05 | 0.00419299 | intron-variant | APAF1 | GRCh38.p7 | 12:98648900 | AATCTTTTGAAGAGA[A/G]TGTGACCAGTTCACT | 317 |
rs762447515 | snp | C/T | 1.69292e-05 | 0.00290935 | intron-variant | APAF1 | GRCh38.p7 | 12:98662657 | TTACTTACTTTGTCT[C/T]GTGATTTTTGTTTGC | 317 |
rs762479508 | snp | A/G | 1.65963e-05 | 0.0028806 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671079 | ACAGACATATACTAG[A/G]TGAAAAGGTATATAT | 317 |
rs762484061 | snp | A/C | 4.96422e-05 | 0.00498183 | intron-variant | APAF1 | GRCh38.p7 | 12:98708582 | TCTTTATCTCTTAAT[A/C]AGCTCTGGGAGACAA | 317 |
rs762490601 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725514 | AGTACCCTGCTGGCA[A/G]CGGGAGATGACAATG | 317 |
rs762549428 | in-del | -/A | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729540 | TGCGGATGGGTTCCT[-/A]AAAGGCCACAGACCA | 317 |
rs762594123 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664007 | CAGTTTTGTTTGTTT[A/G]TTTATTTATTTATTT | 317 |
rs762601497 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648407 | ACATAGAGAAGCTCT[A/G]GAAAAGGACATCAAG | 317 |
rs762608144 | snp | C/G | 1.98037e-05 | 0.00314666 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680320 | TTCTAGAAATCAAGG[C/G]TCATGAGGATGAAGT | 317 |
rs762644156 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713330 | TATCAAGATTTCGCT[A/G]ACTATGCAAAGAGCA | 317 |
rs762663868 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716164 | AGCTTTTAGATGATT[A/C]TTTTGATATTACCTT | 317 |
rs762712144 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680940 | ATTTTAAAATGCAAC[C/T]CCAATTTTTTTAATT | 317 |
rs762737867 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672693 | TTATAATGCTACATA[A/T]TCAAGTTATTCTATT | 317 |
rs762784665 | snp | A/G | 1.68624e-05 | 0.0029036 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708692 | TGCAGTTGACCATAT[A/G]AGACGTCTGCAAGTG | 317 |
rs762810726 | snp | C/T | 3.29973e-05 | 0.00406172 | intron-variant | APAF1 | GRCh38.p7 | 12:98683094 | TTGCCCCTCTGTTCT[C/T]CCTTTGAAAATAATG | 317 |
rs762854460 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693405 | GGCTAACTGATTTTT[A/G]TACATTGATTTTGAT | 317 |
rs762901399 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714228 | AAGTCTTTTAGATAG[C/T]TTAAAAATAAACTCA | 317 |
rs762928753 | snp | A/G | 4.94368e-05 | 0.00497152 | intron-variant | APAF1 | GRCh38.p7 | 12:98659136 | GTTGAAAGGCCTTAA[A/G]TTCATTATTCTTTCC | 317 |
rs762929388 | snp | A/G | 6.69355e-05 | 0.00578475 | intron-variant | APAF1 | GRCh38.p7 | 12:98723364 | TTCTCATATTGCAAT[A/G]ATTATATTGAGACAG | 317 |
rs762945871 | snp | A/G | 1.65419e-05 | 0.00287588 | intron-variant | APAF1 | GRCh38.p7 | 12:98671750 | GAGAAACCAAAGGGA[A/G]TGGTGCGCTAACTAT | 317 |
rs762980809 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656560 | TTTCATGCAGTCACT[A/G]TTCAGTACATTGCCA | 317 |
rs762991931 | snp | C/G | 7.08353e-05 | 0.00595085 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644709 | TCAGACATGTCTGGA[C/G]ACCCTAGGACGACAA | 317 |
rs763046456 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718960 | GGCCTTGTTCTTAGG[A/G]GATCTCTTTGCCCCA | 317 |
rs763064670 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717681 | GTGCCTGGCTTATAT[A/G]TATAATTTTTTCCCC | 317 |
rs763098062 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705361 | TTCTCAAGGGAGATT[G/T]TCAGTTTCTTAGGAG | 317 |
rs763183597 | snp | A/G | 1.78755e-05 | 0.00298955 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735543 | GGCTTTATCAGCTAT[A/G]TGTAAATTCAATTCT | 317 |
rs763208735 | snp | C/T | 1.87767e-05 | 0.00306398 | missense, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732543 | AATCTTGGTATTTTA[C/T]ATATTTTACAGACTT | 317 |
rs763216271 | snp | A/G | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644486 | AACAGCAGGGGGCCC[A/G]CAGGAGGCCGGCCCA | 317 |
rs763232805 | in-del | -/TTCT | | | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735449 | TTTTGGATTGTTTCA[-/TTCT]TTCTTTGCTTGTCAT | 317 |
rs763238156 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | APAF1 | GRCh38.p7 | 12:98715558 | TGAAATTCAGGTGAG[A/G]GGGAGGATGAACTCT | 317 |
rs763247589 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668605 | TAGAGGGGTAGAATC[A/G]TCATGATTTGCTTAT | 317 |
rs763257040 | snp | C/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645946 | GATAACCATCCTGCT[C/T]CTGTACCAGGAAGAG | 317 |
rs763265874 | snp | A/G | 6.6024e-05 | 0.00574523 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665636 | CTCAAACAGCTTCAG[A/G]ATAAGCAGTTTAAGA | 317 |
rs763295435 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698904 | TATCTGGCCCTGCCA[A/G]GCACACAAAGAGTCT | 317 |
rs763301890 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670329 | TTCTCCTTTGATTAC[C/T]GGTGAGATTTTGGCC | 317 |
rs763313470 | in-del | -/T | 0.0212005 | 0.100751 | intron-variant | APAF1 | GRCh38.p7 | 12:98666378 | TGCATCTTGGTTTAC[-/T]TTTTTTTTTCCTTTT | 317 |
rs763317313 | snp | C/G/T | 3.33563e-05 | 0.00408378 | intron-variant | APAF1 | GRCh38.p7 | 12:98648834 | TGTATCCATTATACC[C/G/T]TCTATCACTTTGCTA | 317 |
rs763334786 | snp | A/G | 3.29995e-05 | 0.00406185 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715470 | TCCAGTCCAGGTTTC[A/G]GCACAAGAAAACTGT | 317 |
rs763359913 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659658 | TCAGGAGGCTGAGGC[A/G]GGAGAATCGCTTGAA | 317 |
rs763443228 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683024 | GCATCTTGTCCAACT[A/T]GGAAAATCTGCTATG | 317 |
rs763444312 | snp | C/T | 2.47982e-05 | 0.00352115 | intron-variant | APAF1 | GRCh38.p7 | 12:98699364 | CTAGAAGTGTGATTA[C/T]AGAGTAAAACAAACT | 317 |
rs763463259 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734984 | CAGGTGCGGTGGCAC[A/G]TGCCTGTAATCCCAG | 317 |
rs763464521 | snp | A/G | 0.000115461 | 0.00759718 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712334 | CTCATTAATGGAAGA[A/G]CAGGTCAGATTGATT | 317 |
rs763493399 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644750 | GCTTCTTCACCAGGG[C/G]GAGCAGGACGTGGCC | 317 |
rs763499299 | snp | A/G | 1.69381e-05 | 0.00291011 | intron-variant | APAF1 | GRCh38.p7 | 12:98670938 | ATTTTTTGATCTCTA[A/G]CAGTGCTGCTGATAC | 317 |
rs763506833 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677336 | GGGAACATAACCATG[G/T]TAAAAGACAGTTTAT | 317 |
rs763529331 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697744 | GTAAGCAGAGGTCCT[A/G]CAAAATGATGTTAGA | 317 |
rs763555812 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661315 | TCCTTTTTTGCAAAA[C/T]TAAAATTGACTTCTG | 317 |
rs763556767 | in-del | -/TG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705096 | AGATCTTGAACCTTA[-/TG]TGTAGATCCTCAAAG | 317 |
rs763599650 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690984 | GAGGCCGAGGTGGGC[A/G]GATCATGAGGTCAGG | 317 |
rs763669752 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705111 | TGTGTAGATCCTCAA[A/G]GTAAATGTGGAGCGT | 317 |
rs763706847 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674572 | AGTGATTATCTGTTT[A/G]CTTGGTTTTCTCTCA | 317 |
rs763781521 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702383 | TAAACATTTTAATAG[C/T]TCCCACTGGAAGCTT | 317 |
rs763804980 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | APAF1 | GRCh38.p7 | 12:98725375 | AGATGCTTATTTTGA[A/G]TGTTTATAGCATTGC | 317 |
rs763858103 | snp | A/G | 5.32155e-05 | 0.005158 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644720 | TGGAGACCCTAGGAC[A/G]ACAAGCCCAGGGCAG | 317 |
rs763860807 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703437 | CACAGCACCATCCAG[C/T]ACTGTGACTTCTCCC | 317 |
rs763872979 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679855 | GTGGCTGGACCCCAC[A/G]CTCACTCACACACGC | 317 |
rs763887899 | snp | C/T | 1.84725e-05 | 0.00303906 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644636 | CCCGCCCTCGCTCCG[C/T]TTCCCGGGCTCCGCA | 317 |
rs763913744 | snp | A/G | 1.66194e-05 | 0.00288261 | intron-variant | APAF1 | GRCh38.p7 | 12:98671764 | AGTGGTGCGCTAACT[A/G]TATCATTATTTTTCA | 317 |
rs763920923 | snp | C/T | 3.29995e-05 | 0.00406185 | intron-variant | APAF1 | GRCh38.p7 | 12:98659379 | TTGGTGTGTCAGGTC[C/T]CATGTCCCAATAAGA | 317 |
rs763928339 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706503 | TGGAATACAGACTCA[C/G]GTTCAAAGGTGGCTG | 317 |
rs763974517 | snp | A/C | 1.65067e-05 | 0.00287282 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665661 | TTAAGAGAATAAGGA[A/C]ATCTTCGTCTTATGA | 317 |
rs764010936 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701040 | TTCACATACAGCCTT[G/T]TTGTAACCAATGTAC | 317 |
rs764015461 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668596 | AAGTGATGATAGAGG[G/T]GTAGAATCATCATGA | 317 |
rs764024243 | in-del | -/CAAAGCTAGAATAGGC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721369 | GAACATTGAATCAGG[-/CAAAGCTAGAATAGGC]AGTGTCTGTAAACTA | 317 |
rs764099277 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729243 | CTCTATATCAGCGGT[C/T]CCCAGCCTTTTTGGC | 317 |
rs764102892 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678071 | TGATTTTGCAGAGAA[C/T]ATGATGAAATTAGTT | 317 |
rs764145355 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692394 | AGCCTATGTTTCATG[A/G]TTTAAAAAAAAAAAT | 317 |
rs764160449 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730464 | TCTGGTTTATAAGAT[A/G]TTACAAAGATCAGTG | 317 |
rs764190416 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693469 | TAATCACAATTGAGC[C/T]GTATCGTGTGAATTT | 317 |
rs764198018 | snp | C/G | 8.59439e-05 | 0.00655474 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644511 | GGCCCAGGCAGCCTC[C/G]CGTCCACTTACCAGG | 317 |
rs764223272 | snp | A/C | 1.64882e-05 | 0.00287121 | intron-variant | APAF1 | GRCh38.p7 | 12:98659115 | ACCATTTAAAGGAGT[A/C]CTCCTGTTGAAAGGC | 317 |
rs764266322 | snp | A/G | 1.66588e-05 | 0.00288602 | intron-variant | APAF1 | GRCh38.p7 | 12:98723348 | GTTTTTTGAAAAAGT[A/G]TTCTCATATTGCAAT | 317 |
rs764268296 | snp | A/T | 1.80775e-05 | 0.00300639 | intron-variant | APAF1 | GRCh38.p7 | 12:98699398 | TCTTTTTTATTACTT[A/T]AATTCAAAGCTTTGG | 317 |
rs764323516 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699492 | GACCCTCAAGAGGAT[A/G]TGGAAGTGATAGTGA | 317 |
rs764325283 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697996 | ACAGGGACCCTGGAT[A/G]CAGTGTAGCGACTTG | 317 |
rs764332452 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670423 | TATTTTTTCTCTTGA[C/T]GTGTTTTTCTTTTTC | 317 |
rs764355213 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683150 | CTCTTTAGATTTGGA[A/G]TTCTATGACTGGGGA | 317 |
rs764437457 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727262 | AGGCTGGGTGACTGA[C/T]CTTTGCTTTTCTCCA | 317 |
rs764463198 | snp | C/T | 3.29538e-05 | 0.00405904 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671595 | GGACACCTTCTTGGA[C/T]GACAGCCATTTCCTA | 317 |
rs764470006 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661417 | TCTCAGTCTCATTTG[G/T]TTTGTGCTTTTGTAA | 317 |
rs764482629 | in-del | -/A | 1.64741e-05 | 0.00286998 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671673 | AGCAAGCTAAGCTGC[-/A]AGGCCAAGCAGGAGG | 317 |
rs764496783 | snp | G/T | 1.66482e-05 | 0.0028851 | intron-variant | APAF1 | GRCh38.p7 | 12:98648535 | ACACTTCCTTAAAAA[G/T]TTTTAGAATTTCAGA | 317 |
rs764535985 | snp | A/T | 3.32187e-05 | 0.00407532 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732398 | TACCAATCTAATGAG[A/T]ATTTTATTTTTCTCT | 317 |
rs764543038 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719259 | TTATATTCTTAGCCC[A/C]ACCCTCATTTCCTCC | 317 |
rs764561179 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685196 | TAAATCACCAGAGAT[G/T]ACTATAATCCCTTTT | 317 |
rs764572626 | in-del | -/CAGA | 1.64757e-05 | 0.00287012 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706599 | ACATCTTCTGATGAC[-/CAGA]CAATCAGGGTGAGAA | 317 |
rs764575621 | snp | C/G | 1.7487e-05 | 0.00295689 | intron-variant | APAF1 | GRCh38.p7 | 12:98662841 | TATGAGGAGATTATA[C/G]GGAGTTATATAATTT | 317 |
rs764594572 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667608 | GTATTGGTACAACTT[C/T]CTGGCCTATCACATG | 317 |
rs764614689 | snp | A/C/G | 0.000126347 | 0.00794726 | intron-variant | APAF1 | GRCh38.p7 | 12:98708730 | TTTAGAAAACAATTG[A/C/G]AAAATTGTTTTGGTT | 317 |
rs764623295 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant | APAF1 | GRCh38.p7 | 12:98725381 | TTATTTTGAGTGTTT[A/G]TAGCATTGCTAAACA | 317 |
rs764669890 | snp | C/T | 1.85317e-05 | 0.00304393 | intron-variant | APAF1 | GRCh38.p7 | 12:98683130 | TTGTAAATTTTTTCT[C/T]TTTTCTCTTTAGATT | 317 |
rs764710758 | snp | A/G | 1.76502e-05 | 0.00297066 | intron-variant | APAF1 | GRCh38.p7 | 12:98662420 | GGAAGCTTAAGATAA[A/G]TGTCATTAGTGATTA | 317 |
rs764788511 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700967 | GAATAATATTCCATT[G/T]TATGTATATATCACA | 317 |
rs764813793 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690708 | ATGGTCTGTTCATCC[C/G]TAATTTATTTGCTTT | 317 |
rs764815056 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721813 | AAAAGAAGTAAAAAA[A/G]AGGGGAATAAGAGAT | 317 |
rs764854868 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712993 | TAGCTAATTTTTCTG[-/T]TTTTGTAGAGATGGA | 317 |
rs764871200 | in-del | -/GAGAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689438 | TTTGTGTGAGGGTGA[-/GAGAGA]GAGAGAGAGAGAGAG | 317 |
rs764895219 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725501 | CTTCTCTGTGGACAG[A/T]ACCCTGCTGGCAACG | 317 |
rs764913306 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | APAF1 | GRCh38.p7 | 12:98662574 | TCAGTAATGGGTAAG[A/G]ATTATTCGTTTACTT | 317 |
rs764931291 | in-del | -/GT | 5.00672e-05 | 0.00500311 | downstream-variant-500B, frameshift-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735585 | CTGAGTGCCTCCTCA[-/GT]GTGTCTCTCTGATGG | 317 |
rs764951044 | snp | A/G | 1.777e-05 | 0.00298072 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644730 | AGGACGACAAGCCCA[A/G]GGCAGCTTCTTCACC | 317 |
rs764952058 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706527 | GTGGCTGATTGCAGA[A/G]GACATTTAAGTTGGG | 317 |
rs764992089 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648028 | TGAATGTCTCCTTGA[A/C]GTAAATCCTTAGAAA | 317 |
rs765006856 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677548 | AGCTGATAAAACCTT[A/G]CAGGTAAAACACATC | 317 |
rs765046279 | snp | G/T | 1.66835e-05 | 0.00288816 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735607 | TCTCTGATGGTTCCT[G/T]CCCGGTATGGCTGGC | 317 |
rs765058180 | snp | C/T | 3.6848e-05 | 0.00429216 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680287 | TGCAGGTGTTCAAAG[C/T]TGAAACAGGAGAGAA | 317 |
rs765064029 | snp | A/G | 1.66189e-05 | 0.00288256 | intron-variant | APAF1 | GRCh38.p7 | 12:98665804 | AAGGTAATGGGATCA[A/G]TGATCCTCATCATTG | 317 |
rs765075615 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677766 | GGTGGTAAGGAAGTG[C/T]CCTTTACCCTGCCAG | 317 |
rs765077795 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648382 | CAAAAGCTCGAAATT[A/G]TTTGCTTCAACATAG | 317 |
rs765096279 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728981 | TACTGCTCTGTGGCA[C/T]AATGTTTATGGCTTG | 317 |
rs765098716 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691984 | TCATTCCTAACTTCC[C/T]GCTAGTTGTTGTCAC | 317 |
rs765126284 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661724 | TCCGCCTGCCCTGGC[C/G]TCCCAAAGTGCTGGG | 317 |
rs765160935 | snp | A/G | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643749 | TGCACGGTGATCAAA[A/G]TATGAGCACTCCTCC | 317 |
rs765185635 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656068 | GATTACAGGCATGAG[C/T]CACCGCGCCCGGCCT | 317 |
rs765188930 | snp | G/T | 1.64803e-05 | 0.00287052 | splice-acceptor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98666189 | TTACAACAATTCCTA[G/T]GTGTTATGTATTCTC | 317 |
rs765256155 | snp | A/C | 4.653e-05 | 0.00482316 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644532 | ACTTACCAGGCCAGG[A/C]CCAGGCACGTCCCCA | 317 |
rs765282620 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704038 | TGTATACCTAGCTGG[A/C]CCTGGAAGAATTCCA | 317 |
rs765309528 | snp | A/G/T | 4.05098e-05 | 0.0045004 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644612 | GCTGCTCCGGGCCAC[A/G/T]GGGGTCTTCCCGCCC | 317 |
rs765321160 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727090 | ATAATTTTAGAATAC[A/G]TATATATGGACATAT | 317 |
rs765334055 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705261 | CTTCCTTCTTGAAAT[G/T]TAGGGACTCAGCTCT | 317 |
rs765394902 | snp | G/T | 2.21825e-05 | 0.00333028 | intron-variant | APAF1 | GRCh38.p7 | 12:98671131 | TAAAAAGGAATCTCA[G/T]TTTTTTTTACATTTA | 317 |
rs765395529 | snp | G/T | 1.65312e-05 | 0.00287495 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732414 | ATTTTATTTTTCTCT[G/T]AACAGTGGTGGAACG | 317 |
rs765405502 | snp | A/G | 4.94311e-05 | 0.00497123 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727282 | GCTTTTCTCCAGATG[A/G]CAAAATGCTTATCTC | 317 |
rs765449255 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671612 | ACAGCCATTTCCTAA[C/T]ATTGTACAACTGGGT | 317 |
rs765482627 | in-del | -/TG | 3.8412e-05 | 0.0043823 | intron-variant | APAF1 | GRCh38.p7 | 12:98723622 | AACCTCCAAGTGTTT[-/TG]TTTTTTTTTTTTTAA | 317 |
rs765503614 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667195 | TTAAACTCCTGGGCT[C/T]GGTTGGTCCTGAGTA | 317 |
rs765505499 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682950 | ATATTTGCAAATAAT[A/T]TTTTTTAAACATTAA | 317 |
rs765558556 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668478 | CAAAGTCATTGCTCT[C/G]ACGAGTTTATGTTCT | 317 |
rs765564077 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718155 | TTCTTTCTAGTTTGC[C/T]GTCACTGTCTGTCTA | 317 |
rs765565025 | in-del | -/AAG | 1.76855e-05 | 0.00297362 | intron-variant | APAF1 | GRCh38.p7 | 12:98662413 | TTTAAAAGGAAGCTT[-/AAG]ATAAGTGTCATTAGT | 317 |
rs765579098 | snp | A/G | 1.6522e-05 | 0.00287414 | intron-variant | APAF1 | GRCh38.p7 | 12:98671743 | GTTAGGAGAGAAACC[A/G]AAGGGAGTGGTGCGC | 317 |
rs765585822 | snp | C/T | 0.000115459 | 0.00759712 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712351 | AGGTCAGATTGATTA[C/T]CTGACTGAAGCTCAA | 317 |
rs765587353 | snp | A/T | 1.78605e-05 | 0.0029883 | intron-variant | APAF1 | GRCh38.p7 | 12:98662855 | AGGGAGTTATATAAT[A/T]TCCCTTTTGTTAATT | 317 |
rs765597275 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709324 | TTCTCCTTCTGCCAC[A/C]CAACAAAGAGTGGGA | 317 |
rs765639224 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683235 | CAACAGTAGTCATCA[A/T]CTTCTCTTAGCCACT | 317 |
rs765641337 | snp | A/G | 1.65225e-05 | 0.00287419 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665604 | TACGTGATTTTCCCA[A/G]TCGCTGGGAGTACTA | 317 |
rs765642913 | snp | A/T | 1.65679e-05 | 0.00287814 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715451 | CTTGTAAACAATAGA[A/T]TCTTCCAGTCCAGGT | 317 |
rs765701526 | snp | A/T | 1.66341e-05 | 0.00288388 | intron-variant | APAF1 | GRCh38.p7 | 12:98648819 | TAACTTCGTATGGTT[A/T]GTATCCATTATACCT | 317 |
rs765741073 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659470 | AGAGAGAACCATTGC[A/G]GCCAGGTGCAGTGGC | 317 |
rs765765979 | snp | A/G | 3.85483e-05 | 0.00439006 | intron-variant | APAF1 | GRCh38.p7 | 12:98686725 | ACTAGTTGTTTATTT[A/G]TCTTTTTTTCTTTCA | 317 |
rs765785265 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688904 | ACCACAGTCTATCTC[C/T]TGGGCTTAGATGATC | 317 |
rs765855595 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698170 | TTCTTTGTAAAATTC[A/G]GGCAATAGTTGCTTT | 317 |
rs765914551 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735174 | GGCAGTTCATGCAGT[C/T]GGTCAAGAGGAGGAT | 317 |
rs765965285 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652870 | ACCTCAGGTGATCCC[C/T]CTGCCTCGCCTCCCA | 317 |
rs765971618 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646445 | TTTTCCAAGTGCTAC[A/G]TTTGGTGACTTCAAA | 317 |
rs765980204 | snp | A/G | 3.31472e-05 | 0.00407093 | intron-variant | APAF1 | GRCh38.p7 | 12:98727133 | ACCAGAGAAGCTTCT[A/G]GATAACTCTGTTAAT | 317 |
rs765984017 | snp | G/T | 1.68485e-05 | 0.00290241 | intron-variant | APAF1 | GRCh38.p7 | 12:98662665 | TTTGTCTTGTGATTT[G/T]TGTTTGCAGGTCCTA | 317 |
rs765984453 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706552 | GTTGGGTTCATGGTG[G/T]GATGTTTTCTCCTGA | 317 |
rs766028734 | snp | C/G | 2.36913e-05 | 0.00344167 | intron-variant | APAF1 | GRCh38.p7 | 12:98683095 | TGCCCCTCTGTTCTC[C/G]CTTTGAAAATAATGG | 317 |
rs766034386 | snp | A/G | 1.65356e-05 | 0.00287533 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708593 | TAATCAGCTCTGGGA[A/G]ACAAAGAAAGTATGT | 317 |
rs766035695 | snp | C/T | 1.66095e-05 | 0.00288175 | intron-variant | APAF1 | GRCh38.p7 | 12:98648521 | CTCTGAAGCAGTCCA[C/T]ACTTCCTTAAAAATT | 317 |
rs766046054 | in-del | -/TAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683462 | TGTAACTGAAAAGTC[-/TAGA]TAGAGGGAGCATGGC | 317 |
rs766072509 | in-del | -/AAAG | 3.30688e-05 | 0.00406612 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708596 | TCAGCTCTGGGAGAC[-/AAAG]AAAGTATGTAAGAAC | 317 |
rs766079170 | snp | A/G | 1.68906e-05 | 0.00290603 | downstream-variant-500B, missense | APAF1, ANKS1B | GRCh38.p7 | 12:98735630 | TGGCTGGCATGAAGA[A/G]GATCCTGTAAAAAAG | 317 |
rs766081615 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659968 | GAGTGGTCTTTGCTA[C/G]AAAGTGCAAACTTCT | 317 |
rs766096504 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726689 | TTCCCAGTTATGAGG[C/T]GGTGTTTCATTTTTC | 317 |
rs766119267 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728803 | AACCCAGGTCTCTGC[C/G]TCTGCTTTCTCTAGC | 317 |
rs766131635 | snp | A/G/T | 3.29583e-05 | 0.00405934 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666199 | TCCTAGGTGTTATGT[A/G/T]TTCTCTGGGACATGG | 317 |
rs766133042 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722725 | AGATATTTGAAGCTT[-/G]GGAACTCTTGTGTTT | 317 |
rs766172140 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715235 | GGCATACATGGTGTG[C/T]ATATATATATATATA | 317 |
rs766182126 | snp | A/G | 3.39265e-05 | 0.00411851 | intron-variant | APAF1 | GRCh38.p7 | 12:98723591 | GCTTTTTAATATAAA[A/G]TGTTCTTAAAAGTGT | 317 |
rs766220748 | snp | A/C/G | 4.97445e-05 | 0.004987 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649642 | GGCTGTGGGAAGTCT[A/C/G]TATTAGCTGCAGAAG | 317 |
rs766269001 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703862 | GGCACAGACTCTTTT[C/T]TTCTTAAAAAAGGTG | 317 |
rs766273568 | snp | C/T | 4.9423e-05 | 0.00497082 | intron-variant | APAF1 | GRCh38.p7 | 12:98659150 | AGTTCATTATTCTTT[C/T]CCTCACTAGGTTGTT | 317 |
rs766316399 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652671 | CGCTCTTGTTGCCCA[A/G]GCTGGAGTGCCATGG | 317 |
rs766319681 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676396 | GTATTTTTAGTAGAG[A/T]TGGGGTTTCACCATG | 317 |
rs766348548 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723695 | CTGTCACCAGGGTAC[A/G]GTACTTTCTTGTGAC | 317 |
rs766378928 | snp | G/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731081 | TTGGCCTTGAGATAG[G/T]CTGCCTGAGTTCAAA | 317 |
rs766410773 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716661 | TAGTTTTTATTCATT[A/G]TTTTGGATATTCAGT | 317 |
rs766414508 | snp | C/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733425 | CGTGAGCCACCGTGC[C/G]TGGCCAGGCCCCTTC | 317 |
rs766417490 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667018 | TTTATTATGGGTGAT[A/G]TTAATGTTGATAATT | 317 |
rs766427389 | in-del | -/GTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720655 | AGTATATAGGACTAT[-/GTTA]GTTCTTGCTGGTATG | 317 |
rs766455032 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon, missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732449 | CACTGGGGAATCCTC[A/G]CAGACCTTCTACACA | 317 |
rs766467599 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718071 | GTATGTACACCTTCC[C/T]TTGATCCCTCATTCT | 317 |
rs766516357 | in-del | -/T | 0.0114066 | 0.0746537 | intron-variant | APAF1 | GRCh38.p7 | 12:98662439 | CATTAGTGATTAATA[-/T]TTTTTTTTTAAATTA | 317 |
rs766563241 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680804 | AAAAGCAATGACAAA[G/T]TAGTGAGTTTGTCTT | 317 |
rs766623648 | in-del | -/C | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646488 | GCTTGATAATTATTG[-/C]CCCCCTTCTGTGAGC | 317 |
rs766624750 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717854 | AAGCTCTGTGTGTTG[A/G]CTGAGATCTTCTCTA | 317 |
rs766627138 | snp | C/G | 1.65075e-05 | 0.00287289 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665644 | GCTTCAGAATAAGCA[C/G]TTTAAGAGAATAAGG | 317 |
rs766644403 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732243 | CCATCACCAGTGTTC[A/G]TCAGGAAGAGGCTGA | 317 |
rs766647595 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696629 | CTATTGTCTGTACTC[A/G]CCTGTGCTTGAAACT | 317 |
rs766680485 | snp | A/G | 3.30682e-05 | 0.00406608 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665747 | ATCAAAGATTATTAC[A/G]CAGATCTTTCCATCC | 317 |
rs766780619 | in-del | -/AGAC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692102 | ATTATTATTTTTTTT[-/AGAC]AGAGTCTCGCTCTGT | 317 |
rs766785130 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658402 | CCATAACACTAATAA[C/T]CTGTTTTAATCCTTT | 317 |
rs766832638 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708117 | ATGCCCAGCCAAGTT[G/T]TGTATTTTTAGTAGA | 317 |
rs766860165 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723011 | GCCCCTAGTCAATTT[A/C]CATAACCGCAGCTTC | 317 |
rs766869338 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701441 | ATTTTTCCACAGCAG[-/C]TGCACCGTTTTACAT | 317 |
rs766871252 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674485 | AGCCCCCTAACTTAC[G/T]GAAGCTAGATTAGAT | 317 |
rs766875043 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656964 | ATAACCTTCCTCTTA[C/T]GCTCTTTGTCTGTTA | 317 |
rs766891590 | snp | A/G | 1.68678e-05 | 0.00290407 | intron-variant | APAF1 | GRCh38.p7 | 12:98670943 | TTGATCTCTAACAGT[A/G]CTGCTGATACTACTT | 317 |
rs766941395 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662438 | TCATTAGTGATTAAT[A/G]TTTTTTTTTTAAATT | 317 |
rs766952884 | snp | C/T | 1.66277e-05 | 0.00288333 | intron-variant | APAF1 | GRCh38.p7 | 12:98648527 | AGCAGTCCACACTTC[C/T]TTAAAAATTTTTAGA | 317 |
rs767010301 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725515 | GTACCCTGCTGGCAA[C/T]GGGAGATGACAATGG | 317 |
rs767021293 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726466 | AGGAACAGGTATATA[C/G]TGCAGAAGACTAGGA | 317 |
rs767036586 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710955 | AATTCAGGAGTAGAT[A/T]CTGGGAGTAAATCGC | 317 |
rs767077671 | snp | A/C | 4.94972e-05 | 0.00497455 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648687 | AAAAAGATAATGATT[A/C]CTACGTATCATTCTA | 317 |
rs767084775 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696916 | TACTTCCTGGCTGTT[C/G]TGAACTGTTCAGAAT | 317 |
rs767104968 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659667 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 317 |
rs767120982 | snp | C/T | 3.42132e-05 | 0.00413587 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680354 | TTGTTGTGCATTCTC[C/T]ACAGATGACAGATTT | 317 |
rs767135307 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676140 | GTGACAGGGATGTAA[C/T]GTATATGAAATTCTG | 317 |
rs767166161 | in-del | -/TTTG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672180 | ATTTATTTATTTATT[-/TTTG]AGACAGAGTCTCACT | 317 |
rs767172044 | snp | G/T | 2.23972e-05 | 0.00334635 | intron-variant | APAF1 | GRCh38.p7 | 12:98683112 | TTTGAAAATAATGGA[G/T]ATTTGTAAATTTTTT | 317 |
rs767196364 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701826 | CTTTCTTTCCAATTC[C/T]TATGTGAGTCTACTC | 317 |
rs767196527 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734737 | ATTTAAGCAAATGTG[-/A]AAAAGTGAAACCTTA | 317 |
rs767224954 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689713 | TCCTCCCACTTTGGT[C/T]TCCCAAAGTACTGGG | 317 |
rs767225080 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674689 | GCTCTGCTATTGATT[A/C]GTTGTGTATCATAAG | 317 |
rs767226550 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725078 | CTTATATGAGTTGTC[C/T]TAGTCACAAGAATCT | 317 |
rs767229201 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98729014 | TCCTGCCTTTCAGCA[C/G]CTTACAGTCTATGGG | 317 |
rs767233730 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666308 | TTCGTTATTATTTAC[A/G]TGATCTTCAAGTAGA | 317 |
rs767263068 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718202 | CCCATAGTAACTTTG[G/T]GATTCAACAGCAATT | 317 |
rs767264865 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | APAF1 | GRCh38.p7 | 12:98703327 | AGAATAGCTTATCTC[C/T]TAAAGTATTTTACCT | 317 |
rs767272161 | in-del | -/TGTC | 1.64876e-05 | 0.00287116 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723677 | TAAAGAAAAAGACTT[-/TGTC]TGTCACCAGGGTACA | 317 |
rs767282600 | snp | A/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731444 | CAGGTTGGTGGAATG[A/T]GCTTGATTACACTGT | 317 |
rs767285611 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659264 | TTGGATCAGGATGAG[A/T]GTTTTTCCCAGAGGC | 317 |
rs767289096 | snp | A/T | 3.29478e-05 | 0.00405867 | intron-variant | APAF1 | GRCh38.p7 | 12:98659155 | ATTATTCTTTCCCTC[A/T]CTAGGTTGTTTCCCA | 317 |
rs767290381 | in-del | -/TCTC | 1.66758e-05 | 0.0028875 | downstream-variant-500B, frameshift-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735590 | TGCCTCCTCAGTGTG[-/TCTC]TCTGATGGTTCCTGC | 317 |
rs767323655 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702480 | ATAAAAATCATCTTA[C/T]TTGGCAAAAACTTTG | 317 |
rs767345305 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | APAF1 | GRCh38.p7 | 12:98723804 | CATAAAACTTTGGTA[A/G]TGGTTATGTATAATG | 317 |
rs767350011 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | APAF1 | GRCh38.p7 | 12:98667465 | GTTACTGTGATGCTT[A/G]GGTTATAAAATTGTT | 317 |
rs767385385 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671632 | TACAACTGGGTCTCT[A/G]TGAGCCGGAAACTTC | 317 |
rs767394128 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98665899 | ATAAGACCCAGGGGA[C/T]TGAGGTGGTGGGGTG | 317 |
rs767409373 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667712 | TATTACAAATAAGTG[C/T]TTTTTTTCTGTTATT | 317 |
rs767447642 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666659 | CCTCAAATCTGTGAA[A/G]ATTTATCAGTCTTTA | 317 |
rs767449301 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650003 | GGGTAGAAGAGGGTT[G/T]AAGAAATGTTGGCAG | 317 |
rs767460868 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672958 | AGACAGGGTTTCTCC[A/T]TGTTGGTCAGGCTGG | 317 |
rs767506420 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714968 | CTTCTGATATCCTGT[C/T]TCCCTCATCATCTTT | 317 |
rs767521865 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703418 | AGAAATCCACACGGG[C/T]CATCACAGCACCATC | 317 |
rs767537079 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680204 | TGATTAAACTCACTT[A/C]AAGATTTTTATTGAA | 317 |
rs767557034 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716327 | CACACGTTCACAGAC[A/G]CTCATTTATCAATCC | 317 |
rs767561383 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694341 | TAAACTGCCTACAGA[A/G]TGGTGGCTTCTTTCA | 317 |
rs767562909 | snp | C/T | 1.65822e-05 | 0.00287938 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665785 | GGACGTTAAGGTGCC[C/T]ACAAAGGTAATGGGA | 317 |
rs767600058 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649583 | AGCAGAAGCTCTCCA[A/G]ATTGAAAGGTGAACC | 317 |
rs767661593 | snp | A/T | 2.01945e-05 | 0.00317755 | intron-variant | APAF1 | GRCh38.p7 | 12:98699391 | AACTTTTTCTTTTTT[A/T]TTACTTTAATTCAAA | 317 |
rs767691718 | snp | A/C/G/T | 8.32698e-05 | 0.00645209 | intron-variant | APAF1 | GRCh38.p7 | 12:98649457 | TTCCAAAGTTCTATT[A/C/G/T]ATTCATGCTTGTTTT | 317 |
rs767699613 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715486 | GCACAAGAAAACTGT[A/G]TGGCACATCCAGTTC | 317 |
rs767712620 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98670987 | GGAACTTTGTGCTTT[A/G]ATGTTTTCCCTGGAT | 317 |
rs767714104 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693793 | ACACTTGTTTTTCAG[G/T]TTTTTTTTTTTTTTT | 317 |
rs767754397 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | APAF1 | GRCh38.p7 | 12:98723142 | TCTCCACCCCTCCAA[C/T]GAGATAGGATCGGGG | 317 |
rs767776876 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98663179 | CTGGTGTCTTAATTT[A/G]CATTTTTTTTTAGCG | 317 |
rs767856436 | in-del | -/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688472 | ACTGTTTTCTTTCTT[-/TTT]TTTTTTTTTTTTTTT | 317 |
rs767861971 | snp | A/C | 1.6489e-05 | 0.00287128 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699480 | CTAAATTTGGAGGAC[A/C]CTCAAGAGGATATGG | 317 |
rs767905121 | in-del | -/T | 1.66674e-05 | 0.00288676 | frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662732 | AAAAAGGACTTGAAA[-/T]TTTATCCCTTTTTGT | 317 |
rs767913331 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727245 | GGAGCTGCTACCCAT[A/G]GAGGCTGGGTGACTG | 317 |
rs767956974 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685628 | TGTGAGCCACCACGC[C/T]CAGCTTATAAACTCC | 317 |
rs767988499 | snp | A/G | 1.69677e-05 | 0.00291266 | intron-variant | APAF1 | GRCh38.p7 | 12:98671103 | TATATATATTAACAT[A/G]AAAAATTAGTGCTAA | 317 |
rs768014520 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706885 | ATTTGATTCCTCAGA[A/T]AAATTTTTGACCCTT | 317 |
rs768015266 | snp | A/G | 3.30524e-05 | 0.00406511 | intron-variant | APAF1 | GRCh38.p7 | 12:98727158 | GTTAATGAATTGTGT[A/G]TCATGTTTATGTAGA | 317 |
rs768016167 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708911 | GATAATTCCTCATCT[C/T]ACTGCTCTTCTGTTG | 317 |
rs768082582 | in-del | -/TTTACA | 3.74153e-05 | 0.00432508 | intron-variant | APAF1 | GRCh38.p7 | 12:98671137 | GGAATCTCATTTTTT[-/TTTACA]TTTAATTCTAGATTT | 317 |
rs768104025 | snp | C/T | 1.66205e-05 | 0.00288271 | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648810 | TTAGTGGAATAACTT[C/T]GTATGGTTTGTATCC | 317 |
rs768119868 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652242 | ACAGATGAAAGTCAC[C/T]ATGTCCAGCCAAAAT | 317 |
rs768144818 | snp | A/T | 1.8506e-05 | 0.00304182 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735534 | TTCTATTTAGGCTTT[A/T]TCAGCTATATGTAAA | 317 |
rs768162508 | snp | A/G | 4.95413e-05 | 0.00497677 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665705 | GATGAAGCCATGTCT[A/G]TAAGTGTTGAAATGC | 317 |
rs768199255 | snp | A/C/G | 3.35747e-05 | 0.00409712 | missense, synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715435 | TTTGAAGATTTTAGA[A/C/G]CTTGTAAACAATAGA | 317 |
rs768215449 | snp | A/G | 1.72065e-05 | 0.00293308 | intron-variant | APAF1 | GRCh38.p7 | 12:98648886 | CTTATTGTAGATGTA[A/G]TCTTTTGAAGAGAGT | 317 |
rs768256473 | snp | C/T | 6.59033e-05 | 0.00573997 | intron-variant | APAF1 | GRCh38.p7 | 12:98683321 | AATTTGATTCGTACA[C/T]CAGAGTATCTCCTTT | 317 |
rs768268017 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703530 | TATTCTGTGAAGCCT[A/G]GGTTTCCAGAGATCA | 317 |
rs768316288 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731762 | AGATTCATGGGTAAA[C/T]TTTATGATTCCCATT | 317 |
rs768321120 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704782 | GAAGTGTTTTGTTTT[A/G]TGTTACTTTGTTTTT | 317 |
rs768332131 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693450 | GGGTTTACATCATTG[-/T]AACTAATCACAATTG | 317 |
rs768332699 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696252 | CTTCGGCTGCTTCCA[C/T]TCATGGTGGAAAGGG | 317 |
rs768370588 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650899 | TTATGAACTTTCTTT[G/T]TGTATTTATAATATT | 317 |
rs768457157 | in-del | -/T | 1.65105e-05 | 0.00287315 | intron-variant | APAF1 | GRCh38.p7 | 12:98649480 | TTGTTTTGTTTTGGA[-/T]TTTTAGTAAGGACAG | 317 |
rs768500958 | snp | A/G | 1.6693e-05 | 0.00288898 | intron-variant | APAF1 | GRCh38.p7 | 12:98667694 | CTTCCCTTTTTCCAT[A/G]TGTATTACAAATAAG | 317 |
rs768516013 | snp | A/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733101 | TCCTTTAATTGACTC[A/T]ATAAGTGAGTCTTGG | 317 |
rs768525436 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694963 | CACTGCAAGATGGTG[A/G]ACTTTTGATGTCAAA | 317 |
rs768546773 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725570 | GACATGAGAGCACTG[C/G]TCTTCTTGTAGCTTG | 317 |
rs768551064 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683171 | TGACTGGGGAACTAG[C/T]ACACACCTATGATGA | 317 |
rs768604604 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716181 | TTTGATATTACCTTC[A/G]TGCCTCTATATGGCA | 317 |
rs768615449 | snp | A/C | 1.65976e-05 | 0.00288072 | intron-variant | APAF1 | GRCh38.p7 | 12:98708553 | CATGTTATTTTAGAG[A/C]TGGAATGATAATTTC | 317 |
rs768615855 | snp | A/G | 1.64787e-05 | 0.00287038 | utr-variant-5-prime, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648359 | AAAGATCTGAGGGAA[A/G]ATGGATGCAAAAGCT | 317 |
rs768631377 | snp | A/C | 1.65146e-05 | 0.0028735 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671066 | GAATTTGTGGAATAC[A/C]GACATATACTAGATG | 317 |
rs768637465 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662518 | CTTTTGACAGTCAGT[A/G]TCAGATTCTTCTTAC | 317 |
rs768677050 | in-del | -/ATC | 0.00035224 | 0.0132663 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735533 | TTCTATTTAGGCTTT[-/ATC]ATCAGCTATATGTAA | 317 |
rs768684422 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657688 | TGCAAACAATGCTGC[A/G]GTGAATATTCTTGTG | 317 |
rs768692708 | snp | A/G | 1.70968e-05 | 0.00292371 | intron-variant | APAF1 | GRCh38.p7 | 12:98662641 | TATGTGACATACCAA[A/G]TTACTTACTTTGTCT | 317 |
rs768708171 | in-del | -/AGA | 1.65594e-05 | 0.0028774 | cds-indel, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665766 | ATCTTTCCATCCTTC[-/AGA]AGGACGTTAAGGTGC | 317 |
rs768714954 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686551 | CTTAGTCGATTTACA[C/T]GCTGATCTAAAGGCT | 317 |
rs768735568 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679869 | CGCTCACTCACACAC[A/G]CCTCGCTGTTCCACG | 317 |
rs768735670 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659058 | GAAGTTGAAGATGTG[A/G]TGGGATTGTAAATTG | 317 |
rs768781275 | snp | C/T | 1.65803e-05 | 0.00287922 | intron-variant | APAF1 | GRCh38.p7 | 12:98666370 | CAGGTACTTGCATCT[C/T]GGTTTACTTTTTTTT | 317 |
rs768839143 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673918 | AGGAATTCAAGGGAG[C/G]GTTCCATGAAGGAGA | 317 |
rs768844558 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659223 | AATCTGGGCTTCTGA[C/T]GAAACTGCAGAATCT | 317 |
rs768916963 | snp | A/C | 3.54767e-05 | 0.00421154 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644675 | TCCCTTGGGCCCCGA[A/C]TTCTTCCGGCTCTTC | 317 |
rs768957601 | snp | C/T | 3.29598e-05 | 0.00405941 | splice-donor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98723766 | ACAAGACTGCAAAGG[C/T]AGGTCAATCAATTGA | 317 |
rs768966238 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664829 | CACATGTCGCCACAC[C/G]CAGCTGGATCTTACC | 317 |
rs768970288 | snp | A/T | 1.64811e-05 | 0.00287059 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671718 | CTTTACCTGGAATGG[A/T]TGTAAGTAGGTTAGG | 317 |
rs768971192 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659330 | CGCATTCTGATGCTT[C/T]GCAAACACCCAAGGT | 317 |
rs768972479 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717063 | TTAGTAGAGATGAGA[G/T]TCCACCATGCTGGCC | 317 |
rs768991777 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713334 | AAGATTTCGCTAACT[A/G]TGCAAAGAGCATTTT | 317 |
rs769012939 | snp | G/T | 1.65353e-05 | 0.00287531 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665592 | TTGGTGCACTTTTAC[G/T]TGATTTTCCCAATCG | 317 |
rs769026904 | snp | C/T | 1.66183e-05 | 0.00288251 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644602 | CCCCGCCTCCGCTGC[C/T]CCGGGCCACGGGGGT | 317 |
rs769126565 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702881 | AAACTTGGATTACCC[A/G]AAGTAGTTTTTTGGG | 317 |
rs769135505 | snp | A/G | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729694 | TGAAAACATTCAAGT[A/G]TAGGAGATGATTCTC | 317 |
rs769157410 | snp | A/G | 3.34913e-05 | 0.00409201 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732508 | TGTCCCCTGACTTCA[A/G]AACATATGTGACTGT | 317 |
rs769159250 | in-del | -/TT | 0.00111013 | 0.0235337 | intron-variant | APAF1 | GRCh38.p7 | 12:98723620 | GTCAACCTCCAAGTG[-/TT]TTTTTTTTTTTTTTA | 317 |
rs769232906 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723198 | TGATATTCAGGTATG[G/T]AATTGGCAATTGGAC | 317 |
rs769237137 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | APAF1 | GRCh38.p7 | 12:98686924 | TTATGGAAAGTCTTA[C/T]GATTTGATTATAGAA | 317 |
rs769264932 | snp | A/T | 1.67652e-05 | 0.00289522 | intron-variant | APAF1 | GRCh38.p7 | 12:98677408 | TTAATTTCTGTTCAT[A/T]TTTTCCCTGTATTTA | 317 |
rs769307688 | snp | A/G | 1.65321e-05 | 0.00287502 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671070 | TTGTGGAATACAGAC[A/G]TATACTAGATGAAAA | 317 |
rs769311146 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649540 | CCAGTTGTTTTTGTC[A/T]CAAGGAAGAAGCTGG | 317 |
rs769359806 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713138 | GTACACTTTTATACT[A/G]AATAAATCTTTCTGT | 317 |
rs769388330 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696140 | TTCTGAAACATAATA[C/T]CTGAGACTGGGTAAT | 317 |
rs769413101 | snp | C/T | 1.70064e-05 | 0.00291597 | intron-variant | APAF1 | GRCh38.p7 | 12:98670927 | TTATACCTAAAATTT[C/T]TTGATCTCTAACAGT | 317 |
rs769416375 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716126 | CTTTCCCCCATTTCT[C/T]GTTCTCCAGAGGCAC | 317 |
rs769427886 | snp | A/G | 1.69957e-05 | 0.00291506 | intron-variant | APAF1 | GRCh38.p7 | 12:98662653 | CAAATTACTTACTTT[A/G]TCTTGTGATTTTTGT | 317 |
rs769445933 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679672 | CCCTCTTTGGGGCCC[C/T]GCGGTTCCTGGCATC | 317 |
rs769449478 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710995 | GGTAACTTCTTGTTT[A/G]CTGTGGGTGTCAAAA | 317 |
rs769469396 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717357 | TAGAAATTATATACA[C/T]ACACACACACATATA | 317 |
rs769508417 | snp | C/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731395 | TGAACTAAGTGATCT[C/G]TAAGAGCCTTAGTGA | 317 |
rs769537902 | in-del | -/AAGGTCACAGATCAACAGGATCCCAAG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655148 | CACAGGGTTGGGGGT[-/AAGGTCACAGATCAACAGGATCCCAAG]GCAGAAGAATTTTTC | 317 |
rs769561677 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722133 | TTTTCACGTTTCCCT[C/G]CTCCTATACTTTAAC | 317 |
rs769637846 | snp | A/T | 1.69905e-05 | 0.00291461 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662805 | TATAAAAGAATGTAA[A/T]GGTATGGTTATTTAT | 317 |
rs769639048 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant | APAF1 | GRCh38.p7 | 12:98712294 | CTTACAGCCTAATAA[C/T]TGATTTTGCCTCATT | 317 |
rs769663040 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706492 | TTCTGTAGTTGTGGA[A/G]TACAGACTCACGTTC | 317 |
rs769668394 | in-del | -/T | 1.64806e-05 | 0.00287054 | intron-variant | APAF1 | GRCh38.p7 | 12:98666186 | ACTTACAACAATTCC[-/T]TAGGTGTTATGTATT | 317 |
rs769703045 | snp | C/G | 1.64743e-05 | 0.00287 | missense, intron-variant, splice-acceptor-variant | APAF1 | GRCh38.p7 | 12:98727224 | TGTGCTCCGCTTTCA[C/G]AAGAAGGAGCTGCTA | 317 |
rs769745898 | snp | A/G | 9.88973e-05 | 0.00703128 | intron-variant | APAF1 | GRCh38.p7 | 12:98723786 | CAATCAATTGAAACC[A/G]TGCATAAAACTTTGG | 317 |
rs769794217 | snp | A/G | 1.71496e-05 | 0.00292822 | intron-variant | APAF1 | GRCh38.p7 | 12:98680429 | TTTTCCTCTTGAGTT[A/G]TAATCACAACAGAAT | 317 |
rs769803036 | snp | C/T | 0.000263609 | 0.0114776 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703412 | ATTGGGAGAAATCCA[C/T]ACGGGCCATCACAGC | 317 |
rs769817820 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659246 | CAGAATCTTTGCACA[C/T]GGTTGGATCAGGATG | 317 |
rs769818259 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672198 | GAGACAGAGTCTCAC[C/T]ATGTTGCCAAGGCTG | 317 |
rs769828620 | in-del | -/TTTATTTATC | 1.97543e-05 | 0.00314273 | intron-variant | APAF1 | GRCh38.p7 | 12:98686718 | ACTCAATACTAGTTG[-/TTTATTTATC]TTTTTTTCTTTCACA | 317 |
rs769841126 | snp | A/G | 1.66123e-05 | 0.00288199 | intron-variant | APAF1 | GRCh38.p7 | 12:98648602 | TATTCATTGTTGTAT[A/G]CTAAACTACTTAATT | 317 |
rs769851844 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699165 | CACCATGCAAGACTC[-/T]TTAACTTTTTATTTA | 317 |
rs769860151 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698832 | TGGTCCTACTAGTGA[A/G]CAAAGTTTACAGTAT | 317 |
rs769947936 | snp | A/C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720761 | ACGAGGTCAGGAGAT[A/C/T]GAGACCATCCTGGCT | 317 |
rs769952075 | snp | C/G | 0.000131791 | 0.00811655 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725455 | CACTTCATGAATTGA[C/G]GGGCCACAACGGCTG | 317 |
rs769974597 | snp | A/T | 1.66765e-05 | 0.00288756 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662753 | CCCTTTTTGTTAATA[A/T]GAAGAAGGCAGATTT | 317 |
rs769975027 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645790 | TCTCCCAGTCTTGTC[C/T]CGGCAGTGCCGCCCT | 317 |
rs769977477 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734693 | GTTTTTAAATGGTGG[A/G]TCAAGGAGCTAGTTT | 317 |
rs769991981 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684554 | CATCTCTAACCTCTC[C/T]GCACCACATAGTGCT | 317 |
rs769993350 | snp | C/G | 1.76849e-05 | 0.00297357 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644697 | CGGCTCTTCACCTCA[C/G]ACATGTCTGGAGACC | 317 |
rs770027864 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647113 | ATGATAATGTGTGCT[A/G]AAAAAAATTGACAGT | 317 |
rs770050438 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686490 | AGTAATTGTTTAGTT[A/T]GTTATTTAGTACTCA | 317 |
rs770050548 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670145 | AGTTGAGGTTTCACT[A/G]TGTTGCCCAGGCTGA | 317 |
rs770108783 | snp | C/T | 5.44895e-05 | 0.00521937 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735539 | TTTAGGCTTTATCAG[C/T]TATATGTAAATTCAA | 317 |
rs770122877 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690707 | TATGGTCTGTTCATC[C/G]CTAATTTATTTGCTT | 317 |
rs770153458 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675806 | GTTTGTTTTATCACT[A/T]CTACTAAAGTGTAAT | 317 |
rs770164310 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702551 | AAACTGCGGCTGGGC[A/G]TGGTGGCTCACACCG | 317 |
rs770180034 | snp | C/T | 1.80224e-05 | 0.00300181 | intron-variant | APAF1 | GRCh38.p7 | 12:98648914 | AGTGTGACCAGTTCA[C/T]TGAAAACTGCATGTT | 317 |
rs770194972 | snp | C/T | 1.86371e-05 | 0.00305257 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732536 | TGTGGATAATCTTGG[C/T]ATTTTATATATTTTA | 317 |
rs770288956 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690730 | ATTTGCTTTTCCACT[A/G]GTGCCTATTCTAATC | 317 |
rs770317784 | in-del | -/TGCC | 1.6752e-05 | 0.00289408 | downstream-variant-500B, frameshift-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735574 | TCAAAATTTTCTGAG[-/TGCC]TGCCTCCTCAGTGTG | 317 |
rs770317808 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645795 | CAGTCTTGTCCCGGC[A/G]GTGCCGCCCTCCCCA | 317 |
rs770322698 | snp | C/T | 6.59957e-05 | 0.005744 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648691 | AGATAATGATTCCTA[C/T]GTATCATTCTACAAT | 317 |
rs770350894 | snp | C/G | 1.65206e-05 | 0.00287403 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665724 | GTGTTGAAATGCTCA[C/G]AGAAGACATCAAAGA | 317 |
rs770358022 | in-del | -/TTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672171 | TATTTATTTATTTAT[-/TTA]TTTATTTTTGAGACA | 317 |
rs770359398 | snp | G/T | 1.64917e-05 | 0.00287151 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699549 | GCAAGGATAATGGTG[G/T]CAGCAAAAAATAAAA | 317 |
rs770359491 | snp | A/G | 1.66699e-05 | 0.00288698 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671086 | TATACTAGATGAAAA[A/G]GTATATATATTAACA | 317 |
rs770374669 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713617 | GGTAAAAATATTGTT[A/G]TCTTTATCACAAGTG | 317 |
rs770405143 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679419 | ATTGAGCTATTTTAT[C/T]GCTCAATAAAGCTCC | 317 |
rs770472412 | snp | C/T | 1.71829e-05 | 0.00293106 | intron-variant | APAF1 | GRCh38.p7 | 12:98662818 | AAAGGTATGGTTATT[C/T]ATTTGTTTATGAGGA | 317 |
rs770491067 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694683 | TTTTTTGAAGTTTTC[A/G]TATTCCAGTGTAATA | 317 |
rs770507947 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731281 | CCCCCCACCAGAGAT[A/G]TGCATTTGTTACAAT | 317 |
rs770541633 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713579 | TTGCAAGGCAAAAAT[A/G]TAGTATAATAAAAGG | 317 |
rs770565230 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693039 | CCTTTTCTCTGCAGC[C/T]TCCCTGGCATCTTTT | 317 |
rs770582842 | in-del | -/C | 4.94898e-05 | 0.00497418 | intron-variant | APAF1 | GRCh38.p7 | 12:98723153 | CCAATGAGATAGGAT[-/C]GGGGGAGGATTATAA | 317 |
rs770595178 | snp | A/G | 0.000132094 | 0.00812585 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648639 | AGCCCACTCAACAGC[A/G]AAGAGCAGCTATGCT | 317 |
rs770610441 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727241 | AGAAGGAGCTGCTAC[C/T]CATGGAGGCTGGGTG | 317 |
rs770635496 | in-del | -/A | 3.57414e-05 | 0.00422722 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644746 | GGCAGCTTCTTCACC[-/A]GGGGGAGCAGGACGT | 317 |
rs770676597 | snp | C/T | 1.65861e-05 | 0.00287972 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665560 | TTTTAAAGGCTCTCC[C/T]CTTGTAGTATCTTTA | 317 |
rs770695547 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656040 | CGCCCACCTCGGCCT[A/C]CCAAAGTGCTGGGAT | 317 |
rs770702797 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720503 | TTTGCTGAGCTGAAG[C/T]TATTGCCAAACTTTG | 317 |
rs770735285 | snp | A/C | 1.69017e-05 | 0.00290699 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708693 | GCAGTTGACCATATA[A/C]GACGTCTGCAAGTGA | 317 |
rs770735404 | snp | C/T | 3.35317e-05 | 0.00409448 | intron-variant | APAF1 | GRCh38.p7 | 12:98727368 | GCCTATATCATACTT[C/T]CCAAGCTATTTTCAC | 317 |
rs770748352 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | APAF1 | GRCh38.p7 | 12:98683303 | TTGAGAATTAGGTAG[A/G]TAAATTTGATTCGTA | 317 |
rs770761439 | snp | A/C | 1.65332e-05 | 0.00287512 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648757 | CCTTCTCCATGATGG[A/C]ATTCCTGTTGTCTCT | 317 |
rs770762915 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658342 | TCATGGCCATTCCTA[A/G]TGTTTACTAGTTTGA | 317 |
rs770783336 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669651 | GAATGGCCAGTTGGT[C/T]GATGGACAATTAGAT | 317 |
rs770788246 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | APAF1 | GRCh38.p7 | 12:98712312 | ATTTTGCCTCATTTT[C/T]CATTAGCTCATTAAT | 317 |
rs770791080 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718829 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGTTGGAG | 317 |
rs770802316 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705956 | CTATCCCTTCGCCTC[A/G]CTCTCCCTCCTTCCC | 317 |
rs770822802 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671995 | TTACTGTAATTTAGT[A/G]TAGTGGTGAGGAGCA | 317 |
rs770864896 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662488 | ATGATGTTTGGGACT[C/G]TTGGGTGTTGAAAGC | 317 |
rs770877630 | snp | C/T | 1.67492e-05 | 0.00289384 | intron-variant | APAF1 | GRCh38.p7 | 12:98666391 | ACTTTTTTTTTTCCT[C/T]TTTCCTTTGAAATAA | 317 |
rs770938196 | snp | G/T | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725559 | GGCTGTTTGCTGACA[G/T]GAGAGCACTGCTCTT | 317 |
rs770944215 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649051 | TGTCTACCCTAATTT[G/T]TAGAGACAATAAGAC | 317 |
rs770992106 | snp | C/G | 1.77099e-05 | 0.00297568 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644711 | AGACATGTCTGGAGA[C/G]CCTAGGACGACAAGC | 317 |
rs771023796 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734585 | AGGGTAAGGGAATAG[A/T]TCACTCAGATGTATT | 317 |
rs771038553 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98706805 | GTTCATTGAGGATTA[C/T]CATGGGCCAAGTGCT | 317 |
rs771062804 | snp | A/C/G | 0.000132827 | 0.00814846 | intron-variant | APAF1 | GRCh38.p7 | 12:98708539 | CTTTAAGATGAAGAC[A/C/G]TGTTATTTTAGAGAT | 317 |
rs771107940 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659417 | ACTGACCTCTTGAGA[A/G]CATCATGCCTTTTTC | 317 |
rs771109590 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677170 | ATTAATTAGATTTCT[G/T]CCAACTCAGTGACAT | 317 |
rs771159626 | snp | A/G | 1.73375e-05 | 0.00294422 | intron-variant | APAF1 | GRCh38.p7 | 12:98680249 | TAAGCAGTTTATTAT[A/G]AAAAATATTTTATTG | 317 |
rs771161001 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661062 | TCCCCACCACACGCC[A/G]GGCTAATTTTTTGTA | 317 |
rs771165833 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674597 | CTCTCATACTAGTCC[A/G]TGTGTTCTGAAGTAT | 317 |
rs771167842 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648456 | CACATGATTAGTGAT[A/G]GATTTTTAACAATAT | 317 |
rs771182671 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698722 | GGTTTGGGCATGGGC[A/C]GTCATTATCACTCTG | 317 |
rs771186518 | snp | G/T | 5.30837e-05 | 0.00515161 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735546 | TTTATCAGCTATATG[G/T]AAATTCAATTCTATC | 317 |
rs771188333 | in-del | -/TTTTCACCAGATGATAAGC | 1.64804e-05 | 0.00287053 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686820 | GTCAATCACTGCAGA[-/TTTTCACCAGATGATAAGC]TTTTGGCTAGTTGTT | 317 |
rs771239250 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723212 | GGAATTGGCAATTGG[A/G]CAAATGTATCTTTCT | 317 |
rs771263499 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666253 | CTGCAGGAGTTTGTA[A/G]ATAAGTCTCTTTTAT | 317 |
rs771282420 | snp | A/C | 1.64909e-05 | 0.00287144 | intron-variant | APAF1 | GRCh38.p7 | 12:98666146 | GTCTACAGTCCTGGT[A/C]ATTGTACTTTTGTGG | 317 |
rs771292389 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687970 | GCGCCTGCCACCAAG[C/T]CTGGCTAATTTTTGT | 317 |
rs771307259 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724479 | TCTTTTTCTGCTATA[C/T]TGTTTCCTCTGTGCC | 317 |
rs771309273 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | APAF1 | GRCh38.p7 | 12:98715560 | AAATTCAGGTGAGAG[A/G]GAGGATGAACTCTTA | 317 |
rs771341003 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675576 | CTTGTTATTATTTCC[C/T]AAACACGATGGTATT | 317 |
rs771381529 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694267 | ACAAAAACAAACTTT[A/G]ACAAGTGGAACCTAA | 317 |
rs771430171 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649561 | AAGAAGCTGGTGAAT[A/G]CAATTCAGCAGAAGC | 317 |
rs771437713 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722939 | CTGGTATAATTAACT[G/T]TTCTCCAAGCAACTG | 317 |
rs771447003 | snp | A/G | 1.6516e-05 | 0.00287362 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699452 | GAAAAGCATTAATGT[A/G]AAACAGTTCTTCCTA | 317 |
rs771474216 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705935 | AGAGAAGTCTTGCTT[C/T]CATCCCTATCCCTTC | 317 |
rs771499531 | in-del | -/CTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656743 | TACCTTCTCCATAAC[-/CTT]CTTAAGTGACATGGC | 317 |
rs771504646 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728469 | TCACACCTGTAATCC[A/C]AGCACTTTGGGAGGC | 317 |
rs771508556 | snp | A/G | 8.68555e-05 | 0.0065895 | intron-variant | APAF1 | GRCh38.p7 | 12:98662834 | ATTTGTTTATGAGGA[A/G]ATTATAGGGAGTTAT | 317 |
rs771522663 | in-del | -/T | 0.000551024 | 0.0165894 | intron-variant | APAF1 | GRCh38.p7 | 12:98648616 | TACTAAACTACTTAA[-/T]TTTTTTTAGCCCACT | 317 |
rs771536594 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650604 | AGAGACTTAGAAATA[C/T]GGAGGCTAGGGTATA | 317 |
rs771540360 | snp | A/G | 4.38837e-05 | 0.00468401 | intron-variant | APAF1 | GRCh38.p7 | 12:98649722 | TAGTCTAGTAAGGTA[A/G]ATAGACATGTAAAAA | 317 |
rs771546198 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671705 | CGATAATGGAATGCT[C/T]TACCTGGAATGGATG | 317 |
rs771589815 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652027 | GTCATGTTACCGAGG[C/T]TGGTCTCGAACTCCT | 317 |
rs771602849 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688137 | AGGGAAAAAAGCTTA[A/T]TCAGCCTTCTGAAAT | 317 |
rs771635032 | snp | A/G | 1.65578e-05 | 0.00287726 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665576 | CTTGTAGTATCTTTA[A/G]TTGGTGCACTTTTAC | 317 |
rs771652223 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712319 | CTCATTTTTCATTAG[C/T]TCATTAATGGAAGAA | 317 |
rs771655993 | snp | A/G | 1.70313e-05 | 0.00291811 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715427 | TTTTCTGCTTTGAAG[A/G]TTTTAGAACTTGTAA | 317 |
rs771695263 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705004 | GGCCAGGGTGGTCTC[A/G]AATTCCTGACCTCAA | 317 |
rs771721924 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698204 | TTTTTGTTTTTTAAA[A/T]TTTTTTTAAATTGAA | 317 |
rs771741661 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717913 | TTGTGAGTATCTTCA[C/G]GTCTTTTGTCTTGGT | 317 |
rs771761157 | snp | C/T | 3.29755e-05 | 0.00406038 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677442 | ACAAAAAAAACATCA[C/T]GAATCTTTCCCGCTT | 317 |
rs771813021 | snp | C/T | 3.39064e-05 | 0.00411728 | intron-variant | APAF1 | GRCh38.p7 | 12:98648875 | TTTGGGTTTGTCTTA[C/T]TGTAGATGTAATCTT | 317 |
rs771831357 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734427 | TTAATAGTAGATGTG[C/G]TTCCCAGAAAATATA | 317 |
rs771834365 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677993 | AAAGAATTTCCTTTA[A/T]GATTCCCTTTGTTTT | 317 |
rs771852161 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697319 | TTCAAATGACACCTG[A/G]CATATTTTGTGTTTA | 317 |
rs771871531 | snp | C/G | 3.29473e-05 | 0.00405864 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683197 | GATGAGCACTCAGAG[C/G]AAGTCAATTGCTGCC | 317 |
rs771910922 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668076 | GGCATGAGCCACCGC[A/G]GCTGGCTGAAGATTT | 317 |
rs771928469 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718597 | AGTCCAGCATTTCTA[A/G]CTTCACAGCTCTGCA | 317 |
rs772005315 | in-del | -/TATT | 1.64931e-05 | 0.00287163 | intron-variant | APAF1 | GRCh38.p7 | 12:98703356 | CTTCATAGGTATCTC[-/TATT]TATGTTGACAGCTTT | 317 |
rs772012005 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | APAF1 | GRCh38.p7 | 12:98659351 | CACCCAAGGTACCGA[C/T]GGTCAAATTTAGTTG | 317 |
rs772027707 | snp | A/G | 0.000131781 | 0.00811621 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725466 | TTGAGGGGCCACAAC[A/G]GCTGTGTGCGCTGCT | 317 |
rs772060174 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733197 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACCA | 317 |
rs772084615 | snp | G/T | 0.000156311 | 0.00883918 | intron-variant | APAF1 | GRCh38.p7 | 12:98680264 | AAAAAATATTTTATT[G/T]TTACTTGTGCAGGTG | 317 |
rs772086661 | snp | A/C/T | 3.33157e-05 | 0.00408129 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708673 | AAAATGAAGTGATGG[A/C/T]CCTTGCAGTTGACCA | 317 |
rs772099355 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | APAF1 | GRCh38.p7 | 12:98666174 | TGGCATATTAAATAC[C/T]TACAACAATTCCTAG | 317 |
rs772116915 | snp | A/C | 1.65913e-05 | 0.00288017 | intron-variant | APAF1 | GRCh38.p7 | 12:98667683 | CTTTTATCTGACTTC[A/C]CTTTTTCCATATGTA | 317 |
rs772132639 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654658 | GTGATCCCCTCGCCT[C/T]GGCCTCCCAAAGTTC | 317 |
rs772162064 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707295 | TTTTCCCAAACACTC[C/T]GTAGTTCCCTGCTTC | 317 |
rs772164094 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645264 | GGGCTGGGTGGATCC[A/G]GCGGGATTTGACTGC | 317 |
rs772197509 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657941 | AATAGATCTTTGTGC[A/G]TATATACAAGTATCT | 317 |
rs772199650 | snp | C/G | | | splice-donor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98723313 | GATGGAACAGTGAAG[C/G]TAATTTAAAGTATAA | 317 |
rs772209593 | snp | A/G | 0.000152134 | 0.0087203 | intron-variant | APAF1 | GRCh38.p7 | 12:98680405 | TAAAAAAGTGAAGGT[A/G]GGAAAATCTTTTCCT | 317 |
rs772237159 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696516 | ATCCAATTTCAACAC[A/G]AGTTTGGGTCAGGAT | 317 |
rs772239949 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689226 | CTGCCACATCCTTTC[C/T]TGTCAAGTTTGTTTC | 317 |
rs772304516 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666285 | CTGTGATCGGAATGG[A/G]AAGTCGTTTCGTTAT | 317 |
rs772315089 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709886 | ATTTTCTTTCTTTTG[C/T]TTTTCTTTTGAGACA | 317 |
rs772326353 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659194 | GCATTGGGTTTCAGT[C/T]GGGAAACAAGACAAA | 317 |
rs772347669 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675487 | CTATATCCATAGATT[C/G]AACCAACCTGGATTG | 317 |
rs772350178 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724235 | TGTCAGGGCTGTATC[C/T]TGTCTTTTGTGCTCT | 317 |
rs772365446 | snp | A/T | 1.65072e-05 | 0.00287286 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699559 | TGGTGGCAGCAAAAA[A/T]TAAAATCTTTGTAAG | 317 |
rs772417545 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702016 | GTTTTTGGCCTCCGG[C/T]GCTACGCTGCCTACC | 317 |
rs772431433 | snp | A/G | 2.48296e-05 | 0.00352338 | intron-variant | APAF1 | GRCh38.p7 | 12:98649731 | AAGGTAGATAGACAT[A/G]TAAAAATATTATGAT | 317 |
rs772453065 | snp | G/T | 1.64925e-05 | 0.00287158 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723288 | TTCAAGACTGCTTTC[G/T]TGGTCATTTGATGGA | 317 |
rs772471980 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687876 | GAGTACAATGGTGTG[A/G]TCTTGGCTCACTGCA | 317 |
rs772482875 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671583 | TTATCTTTAAATGGA[C/T]ACCTTCTTGGACGAC | 317 |
rs772495579 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650371 | AGCACCTGTAATCCC[A/G]GCTACTCGGGAGGCT | 317 |
rs772507894 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671301 | TAAGATGTTCAGTGG[-/T]TTTTTTTAAAAAAAG | 317 |
rs772552908 | snp | G/T | 3.33311e-05 | 0.00408221 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723639 | TTTTTTTTTTTTAAG[G/T]TATGGAATATTATTA | 317 |
rs772564707 | snp | C/T | 1.69902e-05 | 0.00291458 | intron-variant | APAF1 | GRCh38.p7 | 12:98670932 | CCTAAAATTTTTTGA[C/T]CTCTAACAGTGCTGC | 317 |
rs772565160 | snp | C/T | 1.73426e-05 | 0.00294466 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644487 | ACAGCAGGGGGCCCA[C/T]AGGAGGCCGGCCCAG | 317 |
rs772577644 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715699 | TTAGATGAAACCTAT[A/G]GGTGTTTCATATTTT | 317 |
rs772580757 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680868 | GTTGAAATCTTTGAG[C/T]GCATTGTGATTAGGA | 317 |
rs772583649 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722725 | AGATATTTGAAGCTT[A/G]GGAACTCTTGTGTTT | 317 |
rs772653492 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649239 | AGTCAGGAAATAATT[C/G]GGTGAGTAAAGCAGA | 317 |
rs772659675 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703395 | ATTCATACTAGTGGC[C/T]TATTGGGAGAAATCC | 317 |
rs772678360 | snp | A/C/T | 6.60702e-05 | 0.00574729 | missense, synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699449 | GAGGAAAAGCATTAA[A/C/T]GTGAAACAGTTCTTC | 317 |
rs772694688 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713286 | CTACTTAGTTGTTTG[A/G]CTGTTCTCCACATAT | 317 |
rs772701293 | snp | C/T | 1.65468e-05 | 0.00287631 | intron-variant | APAF1 | GRCh38.p7 | 12:98662579 | AATGGGTAAGGATTA[C/T]TCGTTTACTTTTTAG | 317 |
rs772740859 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667978 | GGGTTTCACTATGTT[G/T]CTCAGGCTGGTCTCA | 317 |
rs772770863 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726471 | CAGGTATATAGTGCA[A/G]AAGACTAGGAGAGTA | 317 |
rs772792972 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654116 | GTGCCCATAGTCAAG[A/G]TGTTTAGATTCTTTC | 317 |
rs772814348 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692985 | CTTTACAAAGTCACC[A/G]AACAAATTTACATTC | 317 |
rs772816914 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682812 | TCTGACCAGAAATCT[A/G]TTATGCTAACCTCTT | 317 |
rs772870332 | snp | A/T | 1.65589e-05 | 0.00287736 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671076 | AATACAGACATATAC[A/T]AGATGAAAAGGTATA | 317 |
rs772883514 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705108 | TTATGTGTAGATCCT[C/T]AAAGTAAATGTGGAG | 317 |
rs772984932 | snp | A/C | 1.72365e-05 | 0.00293563 | intron-variant | APAF1 | GRCh38.p7 | 12:98680437 | TTGAGTTGTAATCAC[A/C]ACAGAATTCATTTTA | 317 |
rs773008248 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703741 | GCAAGCATTTGCTGA[A/T]TGCCTAACATGTGCC | 317 |
rs773038605 | snp | C/T | 3.14302e-05 | 0.00396411 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680293 | TGTTCAAAGCTGAAA[C/T]AGGAGAGAAACTTCT | 317 |
rs773070279 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727228 | CTCCGCTTTCAGAAG[A/G]AGGAGCTGCTACCCA | 317 |
rs773089739 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734100 | TGAATGGCATTGTGA[A/G]TGCCATTCTTTTAAT | 317 |
rs773107141 | in-del | -/T | 0.0212005 | 0.100751 | intron-variant | APAF1 | GRCh38.p7 | 12:98666377 | TGCATCTTGGTTTAC[-/T]TTTTTTTTTTCCTTT | 317 |
rs773119241 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733283 | GGGACTACAGGTGTG[C/T]GCACATGCCAGGCTA | 317 |
rs773132320 | in-del | -/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643812 | AGCATAATGATATGG[-/T]TTTTCTTTTTTTTTT | 317 |
rs773139246 | snp | C/G/T | 3.29692e-05 | 0.00406001 | synonymous-codon, missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666294 | GAATGGAAAGTCGTT[C/G/T]CGTTATTATTTACAT | 317 |
rs773148827 | snp | A/G | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659337 | TGATGCTTCGCAAAC[A/G]CCCAAGGTACCGATG | 317 |
rs773181328 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681599 | TCCTGAAGTTTTCAC[C/T]TACTGGAAGAGGGCT | 317 |
rs773195005 | snp | A/T | 3.32022e-05 | 0.00407431 | intron-variant | APAF1 | GRCh38.p7 | 12:98648607 | ATTGTTGTATACTAA[A/T]CTACTTAATTTTTTT | 317 |
rs773198742 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673435 | GTGAAGCTCTGTCTC[-/A]AAAAAACAAAAAAAA | 317 |
rs773198834 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666883 | TAGAGATAGTGTTTT[A/G]CCATGTTGCCCAGGC | 317 |
rs773205052 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732180 | CAGGCTGCATGTTTC[C/T]CCAGCACAACTCAAC | 317 |
rs773212660 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683180 | AACTAGTACACACCT[A/T]TGATGAGCACTCAGA | 317 |
rs773237250 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718007 | GTTCTCAGAGCTAAG[C/T]TGGGGAAGATAACAG | 317 |
rs773265772 | snp | A/G | 4.94262e-05 | 0.00497098 | intron-variant | APAF1 | GRCh38.p7 | 12:98706441 | TTTGCTCTCTTCAAA[A/G]TGCTTATGTATGTGA | 317 |
rs773274132 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674386 | GCCATTTCCCTCCTA[C/G]CTTCCCACTTTCCAG | 317 |
rs773318734 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677464 | TTCCCGCTTAGTTGT[C/T]CGCCCCCACACAGAT | 317 |
rs773325915 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645957 | TGCTCCTGTACCAGG[A/G]AGAGAAATTCTGTAA | 317 |
rs773332119 | snp | A/T | 3.53638e-05 | 0.00420484 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644701 | TCTTCACCTCAGACA[A/T]GTCTGGAGACCCTAG | 317 |
rs773341738 | snp | C/T | 3.29723e-05 | 0.00406018 | intron-variant | APAF1 | GRCh38.p7 | 12:98659348 | AAACACCCAAGGTAC[C/T]GATGGTCAAATTTAG | 317 |
rs773360952 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672661 | GATAGCTATTAATAC[C/T]ATCTTTTTAATGCCT | 317 |
rs773373410 | in-del | -/ACTGGGTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708316 | TTATCTTTGAGTAAC[-/ACTGGGTT]AAGCAACCTGCCTGA | 317 |
rs773415353 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658126 | TTATGATTGATGCTA[C/T]TGGAATGATCTAATG | 317 |
rs773435057 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697369 | TTACTTCCCTTACTG[G/T]CCTGTCAACTCATTG | 317 |
rs773445196 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717649 | CCAATGTGCTGGGAT[G/T]ACAGGCATGAGCCAC | 317 |
rs773476745 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724267 | TTGATGACTCTTTAG[A/T]GCATCTTAGAGTTAT | 317 |
rs773513071 | in-del | -/C | 6.67791e-05 | 0.00577798 | downstream-variant-500B, frameshift-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735582 | TTCTGAGTGCCTCCT[-/C]CAGTGTGTCTCTCTG | 317 |
rs773514371 | in-del | -/ATTA | 0.000104413 | 0.00722466 | intron-variant | APAF1 | GRCh38.p7 | 12:98662432 | TAAGTGTCATTAGTG[-/ATTA]ATATTTTTTTTTTAA | 317 |
rs773526670 | snp | A/G | 1.65214e-05 | 0.0028741 | intron-variant | APAF1 | GRCh38.p7 | 12:98671744 | TTAGGAGAGAAACCA[A/G]AGGGAGTGGTGCGCT | 317 |
rs773530484 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687925 | CAAGCGATTCTCGTG[C/T]CCCAGTCTCCCAAGT | 317 |
rs773534244 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672650 | AAAAAGGAAAGGATA[C/G]CTATTAATACCATCT | 317 |
rs773561445 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708003 | CCAGGCTGGAGTGCA[A/G]TGGCACTATCTTGGC | 317 |
rs773569845 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700152 | GTATTTGTGGTATTC[-/A]AGAGTGCCCTCACAT | 317 |
rs773574010 | snp | C/T | 1.65233e-05 | 0.00287426 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665606 | CGTGATTTTCCCAAT[C/T]GCTGGGAGTACTACC | 317 |
rs773587844 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674232 | CCTGGACACAATTGA[A/T]CCTCCTTCCTTGACT | 317 |
rs773591717 | snp | A/G | 1.651e-05 | 0.0028731 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715463 | AGAATCTTCCAGTCC[A/G]GGTTTCAGCACAAGA | 317 |
rs773614557 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709095 | TCTTTGAAAGAACAG[A/T]AGTCACTTTAGGTGA | 317 |
rs773646112 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702050 | TGTGCATGCTTGCAG[G/T]GACTATGCATTCACT | 317 |
rs773649524 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722878 | AGGAAAATTTAATCA[G/T]ATGGTGAGCTCACTG | 317 |
rs773664804 | snp | A/C | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662535 | CAGATTCTTCTTACA[A/C]CCAGAGACAAGAGTG | 317 |
rs773669118 | snp | C/T | 1.86604e-05 | 0.00305448 | intron-variant | APAF1 | GRCh38.p7 | 12:98648924 | GTTCACTGAAAACTG[C/T]ATGTTAAAAAAATTG | 317 |
rs773698509 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690975 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAT | 317 |
rs773700554 | snp | C/G | 1.65198e-05 | 0.00287395 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665726 | GTTGAAATGCTCAGA[C/G]AAGACATCAAAGATT | 317 |
rs773751622 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693453 | TTTACATCATTGTAA[A/C]TAATCACAATTGAGC | 317 |
rs773754048 | snp | A/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727243 | AAGGAGCTGCTACCC[A/T]TGGAGGCTGGGTGAC | 317 |
rs773763415 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687020 | TTAATGTAACTGTAA[C/T]TGCTTATCGTAATGA | 317 |
rs773765371 | snp | G/T | 1.65026e-05 | 0.00287246 | intron-variant | APAF1 | GRCh38.p7 | 12:98686925 | TATGGAAAGTCTTAT[G/T]ATTTGATTATAGAAA | 317 |
rs773770783 | in-del | -/TAAAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681845 | CCTATTAAAGAACTT[-/TAAAA]TAAGATAAACTCTCT | 317 |
rs773776704 | snp | C/T | 1.66134e-05 | 0.00288208 | intron-variant | APAF1 | GRCh38.p7 | 12:98648523 | CTGAAGCAGTCCACA[C/T]TTCCTTAAAAATTTT | 317 |
rs773784439 | in-del | -/GAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720109 | AAAACTACATCTGAT[-/GAA]GTTCTTTTGAGACAT | 317 |
rs773794530 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649245 | GAAATAATTGGGTGA[A/G]TAAAGCAGATATAGA | 317 |
rs773840959 | snp | C/G | 3.29522e-05 | 0.00405894 | intron-variant | APAF1 | GRCh38.p7 | 12:98662671 | TTGTGATTTTTGTTT[C/G]CAGGTCCTAAATATG | 317 |
rs773868732 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717750 | AAGTTGCTTTTTTCT[C/G]TTTGGTTGTTTTGAC | 317 |
rs773894374 | snp | C/T | 1.72785e-05 | 0.00293921 | intron-variant | APAF1 | GRCh38.p7 | 12:98662826 | GGTTATTTATTTGTT[C/T]ATGAGGAGATTATAG | 317 |
rs773902530 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658464 | ATCATTAATTTTTCA[C/G]AGCAACTCTGAAATA | 317 |
rs773960391 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689661 | AGATGGGGCCTCCCT[A/G]TGTTACCCAGGCTGG | 317 |
rs773985785 | snp | A/G | 1.66768e-05 | 0.00288758 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732381 | TTGTCACACAGTGTA[A/G]TTACCAATCTAATGA | 317 |
rs774056691 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675122 | TTAAATTGTGTTTGA[C/T]CAGTCCATATTCAAA | 317 |
rs774076296 | snp | C/T | 1.69542e-05 | 0.0029115 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708696 | GTTGACCATATAAGA[C/T]GTCTGCAAGTGAGTA | 317 |
rs774078486 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648666 | TGCTGATTAAAATGA[C/T]ACTTAAAAAAGATAA | 317 |
rs774095537 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723699 | CACCAGGGTACAGTA[A/C]TTTCTTGTGACATTT | 317 |
rs774103915 | snp | A/G | 1.69714e-05 | 0.00291298 | intron-variant | APAF1 | GRCh38.p7 | 12:98666405 | TTTTTCCTTTGAAAT[A/G]ATTTTAGATTTATTG | 317 |
rs774106132 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681425 | GCTTCTACCAGGAGC[A/T]TTTATACTAATATAG | 317 |
rs774137714 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716258 | CGAATTCCCTACAGG[A/C]AGATGTTGCTTTTTT | 317 |
rs774171361 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659248 | GAATCTTTGCACACG[A/G]TTGGATCAGGATGAG | 317 |
rs774204904 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | APAF1 | GRCh38.p7 | 12:98712313 | TTTTGCCTCATTTTT[C/T]ATTAGCTCATTAATG | 317 |
rs774252639 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683185 | GTACACACCTATGAT[A/G]AGCACTCAGAGCAAG | 317 |
rs774346140 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667553 | AGTTTCAGAGATATC[A/G]CCAGCCGCATACTCT | 317 |
rs774377509 | in-del | -/TGAT | 2.49144e-05 | 0.00352938 | intron-variant | APAF1 | GRCh38.p7 | 12:98699357 | AAAATTCTAGAAGTG[-/TGAT]TGATTATAGAGTAAA | 317 |
rs774388902 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731807 | AAATATTATAAGCAA[A/G]TTCAGTGATTGGGAA | 317 |
rs774406993 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716512 | GAAGACATTGCTCCA[-/T]TTTCTTCCAAGTTCC | 317 |
rs774411275 | snp | A/C | 1.64868e-05 | 0.00287109 | intron-variant | APAF1 | GRCh38.p7 | 12:98723796 | AAACCATGCATAAAA[A/C]TTTGGTAGTGGTTAT | 317 |
rs774480986 | snp | C/G | 1.64787e-05 | 0.00287038 | utr-variant-5-prime, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648350 | CAGAGAGAGAAAGAT[C/G]TGAGGGAAGATGGAT | 317 |
rs774499367 | snp | C/T | 3.29511e-05 | 0.00405887 | intron-variant | APAF1 | GRCh38.p7 | 12:98715586 | TCTTAACATATTTAA[C/T]GCTGATTCTAGCAAA | 317 |
rs774512133 | in-del | -/AG | 0.000346098 | 0.0131503 | utr-variant-5-prime, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648336 | CATGGTTGACAGCTC[-/AG]AGAGAGAAAGATCTG | 317 |
rs774554248 | snp | A/T | 6.93441e-05 | 0.00588789 | intron-variant | APAF1 | GRCh38.p7 | 12:98699379 | TAGAGTAAAACAAAC[A/T]TTTTCTTTTTTATTA | 317 |
rs774555968 | in-del | -/T | 0.00149831 | 0.0273297 | intron-variant | APAF1 | GRCh38.p7 | 12:98671131 | TAAAAAGGAATCTCA[-/T]TTTTTTTTACATTTA | 317 |
rs774566477 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647706 | GGGATCATGTTTCTG[G/T]TTTTTTTTTTTTTTT | 317 |
rs774596730 | snp | C/T | 6.62032e-05 | 0.00575302 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665761 | CACAGATCTTTCCAT[C/T]CTTCAGAAGGACGTT | 317 |
rs774605842 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657830 | TCCTCATTTTCAAAA[G/T]GAAGATAATAGTGTC | 317 |
rs774654988 | snp | A/G | 3.39368e-05 | 0.00411913 | downstream-variant-500B, synonymous-codon | APAF1, ANKS1B | GRCh38.p7 | 12:98735563 | AATTCAATTCTATCA[A/G]AATTTTCTGAGTGCC | 317 |
rs774796950 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686611 | TTTTGTGTTTGATAC[A/G]TTTGTGTTACTGTGA | 317 |
rs774817570 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649041 | GATAATAATATGTCT[A/C]CCCTAATTTTTAGAG | 317 |
rs774818579 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688472 | CACTGTTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 317 |
rs774830724 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701640 | AAAGATTTTAAGAGA[-/C]CTGTTCTAGTGAGAG | 317 |
rs774840943 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649562 | AGAAGCTGGTGAATG[C/T]AATTCAGCAGAAGCT | 317 |
rs774849783 | snp | A/G | 1.67234e-05 | 0.00289161 | intron-variant | APAF1 | GRCh38.p7 | 12:98671089 | ACTAGATGAAAAGGT[A/G]TATATATTAACATGA | 317 |
rs774877020 | snp | A/G | 1.65091e-05 | 0.00287303 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699457 | GCATTAATGTGAAAC[A/G]GTTCTTCCTAAATTT | 317 |
rs774884721 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713402 | AAGTTGTTTCCATTT[C/T]GGTACTGATAAGGCT | 317 |
rs774892171 | snp | A/G | 2.31425e-05 | 0.00340158 | intron-variant | APAF1 | GRCh38.p7 | 12:98649725 | TCTAGTAAGGTAGAT[A/G]GACATGTAAAAATAT | 317 |
rs774906739 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667825 | TTCTCAGGCTGGAGT[A/G]CAGTGGCACAATCTC | 317 |
rs774943331 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694076 | AACTGGCTAGCCATA[C/T]GCAGAAGAATGAAAC | 317 |
rs774964306 | snp | C/G | 0.000230981 | 0.0107442 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648688 | AAAAGATAATGATTC[C/G]TACGTATCATTCTAC | 317 |
rs774966225 | snp | C/T | 6.61605e-05 | 0.00575116 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665588 | TTAATTGGTGCACTT[C/T]TACGTGATTTTCCCA | 317 |
rs774976361 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662034 | GTAAAAAATGGTCAC[A/G]TATCATCATTATTGT | 317 |
rs775021247 | snp | C/G | 4.96331e-05 | 0.00498138 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648769 | TGGCATTCCTGTTGT[C/G]TCTTCTTCCAGTGGT | 317 |
rs775076443 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659666 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 317 |
rs775079178 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688115 | AGGTAGGAAAAATGC[A/G]AGAGTTAGGGAAAAA | 317 |
rs775082489 | in-del | -/GTTTTGCCTAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689006 | TTTATTAGAGATGGG[-/GTTTTGCCTAT]GTTTCCCAGGCTGGT | 317 |
rs775099681 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650797 | GATTTTTTTAAGCCC[C/G]TACTGCAAAGTTGAT | 317 |
rs775142739 | snp | A/T | 1.69677e-05 | 0.00291266 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715429 | TTCTGCTTTGAAGAT[A/T]TTAGAACTTGTAAAC | 317 |
rs775163513 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679769 | CCAGCCACAGCCTCA[C/T]AGAGAGCCAGAGCCC | 317 |
rs775176080 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704940 | GCCCACCAGCATGCC[C/T]GGCTAATTTTTTTTT | 317 |
rs775277185 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731411 | TAAGAGCCTTAGTGA[C/T]TGAAAACAAATGAAT | 317 |
rs775291215 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | APAF1 | GRCh38.p7 | 12:98667467 | TACTGTGATGCTTAG[A/G]TTATAAAATTGTTTC | 317 |
rs775321405 | in-del | -/T | 5.02281e-05 | 0.00501114 | intron-variant | APAF1 | GRCh38.p7 | 12:98648855 | ACTTTGCTATCAAAA[-/T]TTGCTTTGGGTTTGT | 317 |
rs775323050 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678653 | GGCATCCCTGTACTC[C/T]TGGGGGACCTGGAAG | 317 |
rs775325950 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714844 | AAGCCTTTTTTTTTC[-/T]TTTTTTTTTTTTGAC | 317 |
rs775334036 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716127 | TTTCCCCCATTTCTC[A/G]TTCTCCAGAGGCACC | 317 |
rs775336955 | snp | G/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725471 | GGGCCACAACGGCTG[G/T]GTGCGCTGCTCTGCC | 317 |
rs775344183 | snp | A/G/T | 3.29529e-05 | 0.00405901 | intron-variant | APAF1 | GRCh38.p7 | 12:98683316 | AGATAAATTTGATTC[A/G/T]TACATCAGAGTATCT | 317 |
rs775344984 | in-del | -/AA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675310 | ATATCCTTTATTATG[-/AA]AGTCACTTTCTGAGC | 317 |
rs775371165 | snp | A/G | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730385 | TCAGCTTTGACACCA[A/G]GTTTCTAGAGACCAC | 317 |
rs775397727 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667582 | CTTTCACCAGATCAG[A/G]AAGACTGTATGTATT | 317 |
rs775401339 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686519 | CAGCCTAAAAACCTC[A/G]GTGAGCCTTTGAGTC | 317 |
rs775421938 | in-del | -/GTACT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678025 | AGAAAATATTAATGA[-/GTACT]TTTCTTTATGTTTGT | 317 |
rs775461454 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | APAF1 | GRCh38.p7 | 12:98706482 | GCTGTGTTTATTCTG[C/T]AGTTGTGGAATACAG | 317 |
rs775463511 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693371 | AGTGCTGGGCTTACA[A/G]GCATGAACCACTGTG | 317 |
rs775507125 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662491 | ATGTTTGGGACTCTT[C/G]GGTGTTGAAAGCTTT | 317 |
rs775514151 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707302 | AAACACTCCGTAGTT[C/G]CCTGCTTCTGTGCTT | 317 |
rs775518444 | in-del | -/C | 1.64772e-05 | 0.00287025 | intron-variant, frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703412 | ATTGGGAGAAATCCA[-/C]ACGGGCCATCACAGC | 317 |
rs775537135 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727291 | CAGATGGCAAAATGC[C/T]TATCTCTGCTGGAGG | 317 |
rs775551448 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667113 | GTATATATATATGTA[-/T]TTTTTTTTTTTTGAG | 317 |
rs775588952 | snp | A/G | 2.5434e-05 | 0.003566 | intron-variant | APAF1 | GRCh38.p7 | 12:98649733 | GGTAGATAGACATGT[A/G]AAAATATTATGATAT | 317 |
rs775597203 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662800 | AGTATTATAAAAGAA[-/TG]TAAAGGTATGGTTAT | 317 |
rs775606666 | in-del | -/T/TT/TTT | 0.479507 | 0.126302 | intron-variant | APAF1 | GRCh38.p7 | 12:98723619 | GTCAACCTCCAAGTG[-/T/TT/TTT]TTTTTTTTTTTTTTT | 317 |
rs775615293 | snp | C/T | 1.64827e-05 | 0.00287073 | intron-variant | APAF1 | GRCh38.p7 | 12:98666177 | CATATTAAATACTTA[C/T]AACAATTCCTAGGTG | 317 |
rs775624899 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723501 | TTATACTGTTAGTCA[C/T]ATTTAAAGTAAAGGG | 317 |
rs775633157 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647254 | AACCCCGTCTGTACT[A/G]AAAAAAAAAAAAAAA | 317 |
rs775644489 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699485 | TTTGGAGGACCCTCA[A/G]GAGGATATGGAAGTG | 317 |
rs775647653 | snp | C/G/T | 3.29664e-05 | 0.00405984 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666290 | ATCGGAATGGAAAGT[C/G/T]GTTTCGTTATTATTT | 317 |
rs775659227 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703280 | AATTGTCATATTTTT[C/T]TCAGGACTTATATTT | 317 |
rs775677161 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697696 | TGTTAAGTCAGTATC[A/G]TTGGTTGGTTCACAC | 317 |
rs775683789 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98670165 | GCCCAGGCTGATCTT[A/G]ACCCCTGGGCTCGAG | 317 |
rs775699465 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661312 | TTTTCCTTTTTTGCA[A/T]AATTAAAATTGACTT | 317 |
rs775738729 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672208 | CTCACTATGTTGCCA[A/G]GGCTGGAGTGCAGTG | 317 |
rs775782347 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712264 | AAGCCTCTGTTCTGA[C/T]GAACAAAAACTGCTC | 317 |
rs775798433 | snp | A/G | 1.65501e-05 | 0.00287659 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723310 | TTTGATGGAACAGTG[A/G]AGGTAATTTAAAGTA | 317 |
rs775866105 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645805 | CCGGCAGTGCCGCCC[A/T]CCCCACTAAGACCTA | 317 |
rs775893970 | in-del | -/TTTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712226 | TGGTTATTTTCTGTG[-/TTTTA]TTTTATTTTTTTCAA | 317 |
rs775903350 | in-del | -/CGAGGCGGGCGGATCA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720731 | GGCACTTTGGGAGGC[-/CGAGGCGGGCGGATCA]CGAGGTCAGGAGATC | 317 |
rs775922661 | snp | A/C | 1.66189e-05 | 0.00288256 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723646 | TTTTTAAGGTATGGA[A/C]TATTATTACTGGAAA | 317 |
rs775928461 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677326 | TTGTATTTTGGGGAA[C/T]ATAACCATGTTAAAA | 317 |
rs775962792 | in-del | -/CCT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653984 | TGCTACCAGGATAAG[-/CCT]CCTGTGAAAGTAGTG | 317 |
rs776002033 | snp | A/G | 3.49199e-05 | 0.00417836 | intron-variant | APAF1 | GRCh38.p7 | 12:98648896 | ATGTAATCTTTTGAA[A/G]AGAGTGTGACCAGTT | 317 |
rs776005626 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727249 | CTGCTACCCATGGAG[A/G]CTGGGTGACTGACCT | 317 |
rs776015387 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728255 | AAATCTTTAAAAAAA[C/T]ATATTTTTGAAATTT | 317 |
rs776028107 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671590 | TAAATGGACACCTTC[C/T]TGGACGACAGCCATT | 317 |
rs776055850 | snp | A/G | | | intron-variant, upstream-variant-2KB | IKBIP, APAF1 | GRCh38.p7 | 12:98643243 | GGTGTGAGCCACCGC[A/G]CCCAGCCGTAACAAA | 317 |
rs776110169 | snp | A/T | 8.2373e-05 | 0.00641714 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667591 | GATCAGGAAGACTGT[A/T]TGTATTGGTACAACT | 317 |
rs776182563 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679643 | TGGGAGCTCCCCAAG[A/C]TAGGGCTGTGACTCC | 317 |
rs776209168 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678565 | GCAGGCTCGGGCCTC[C/T]GGCTCCACAGAGCAG | 317 |
rs776282437 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682662 | TCATGTTCATTATCT[C/G]ATTTGATATCTTAAA | 317 |
rs776313306 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725575 | GAGAGCACTGCTCTT[C/T]TTGTAGCTTGGGCTA | 317 |
rs776327563 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656421 | AACTTTAGGAGTAAG[C/G]AGTAGGGCTTGTCTA | 317 |
rs776360721 | snp | G/T | 1.70801e-05 | 0.00292229 | intron-variant | APAF1 | GRCh38.p7 | 12:98670924 | ATGTTATACCTAAAA[G/T]TTTTTGATCTCTAAC | 317 |
rs776369613 | in-del | -/TACT | 1.64851e-05 | 0.00287093 | intron-variant | APAF1 | GRCh38.p7 | 12:98666171 | TTGTGGCATATTAAA[-/TACT]TACAACAATTCCTAG | 317 |
rs776387511 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725496 | TCTGCCTTCTCTGTG[G/T]ACAGTACCCTGCTGG | 317 |
rs776444753 | in-del | -/TGAGGTCAGGAGTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727724 | GGTGGGCGGATCACC[-/TGAGGTCAGGAGTT]TGAGACCAGCCTGGC | 317 |
rs776457513 | snp | C/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645858 | GACCTCCTCGCTTTT[C/T]TCCCCGAGCCAGGTT | 317 |
rs776465989 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98729952 | TAGTTAACAATTTAT[C/T]GTATATTTCAAAATA | 317 |
rs776468871 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98656059 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACCGC | 317 |
rs776474806 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684014 | CCCAGAAAGATCTGC[-/T]AACTTTTTTTGAATT | 317 |
rs776516384 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734647 | ATAAATACAGTGAAT[A/G]CAATCCTTTGCATTG | 317 |
rs776548359 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718848 | CTGAGGTTGGAGGAT[C/T]GCTTGAGCCTAGGAG | 317 |
rs776549603 | in-del | -/A | 3.29457e-05 | 0.00405854 | frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659170 | ACTAGGTTGTTTCCC[-/A]GGGGGAGTGCATTGG | 317 |
rs776551018 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690753 | TTCTAATCCTTTTCT[-/G]CTGTTCTTAAGCCCC | 317 |
rs776591844 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668215 | TAGTAAAAATGGGAT[C/T]ATAGCTTGCATAATT | 317 |
rs776603289 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705165 | ACTAAGTAGCAACCC[C/G]TCTTTCAGCCTTTCT | 317 |
rs776606994 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648375 | ATGGATGCAAAAGCT[C/G]GAAATTGTTTGCTTC | 317 |
rs776607206 | snp | G/T | 8.52624e-05 | 0.0065287 | intron-variant | APAF1 | GRCh38.p7 | 12:98662647 | ACATACCAAATTACT[G/T]ACTTTGTCTTGTGAT | 317 |
rs776611505 | snp | A/G | 7.03062e-05 | 0.00592859 | intron-variant | APAF1 | GRCh38.p7 | 12:98680267 | AAATATTTTATTGTT[A/G]CTTGTGCAGGTGTTC | 317 |
rs776613503 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655994 | TTCACCGTGTTAGCC[A/G]GGATGGTTTCGATCT | 317 |
rs776665787 | in-del | -/CAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98721169 | CAGTGTGTTTCCGTG[-/CAA]CAACAACAACAACAA | 317 |
rs776681072 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | APAF1 | GRCh38.p7 | 12:98659121 | TAAAGGAGTACTCCT[A/G]TTGAAAGGCCTTAAG | 317 |
rs776687272 | snp | A/C | 1.6649e-05 | 0.00288518 | intron-variant | APAF1 | GRCh38.p7 | 12:98666376 | CTTGCATCTTGGTTT[A/C]CTTTTTTTTTTCCTT | 317 |
rs776724492 | snp | C/T | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734837 | CACACTGTTAGGGGC[C/T]CATCTCATGTAGGCA | 317 |
rs776731061 | snp | A/C | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648475 | TTTTAACAATATCAG[A/C]AGAGGAAAAAGTAAG | 317 |
rs776741226 | snp | C/G | 2.1219e-05 | 0.00325716 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644604 | CCGCCTCCGCTGCTC[C/G]GGGCCACGGGGGTCT | 317 |
rs776770955 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661072 | ACGCCGGGCTAATTT[G/T]TTGTATTTTTAGTAG | 317 |
rs776799189 | snp | C/T | 1.64806e-05 | 0.00287054 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723687 | GACTTTGTCTGTCAC[C/T]AGGGTACAGTACTTT | 317 |
rs776814584 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709285 | TGTATTGCTTAGGGA[A/T]CCAAACAGCACTACT | 317 |
rs776815411 | snp | C/T | 6.00474e-05 | 0.00547906 | upstream-variant-2KB, stop-gained, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644523 | CTCGCGTCCACTTAC[C/T]AGGCCAGGCCCAGGC | 317 |
rs776837005 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697596 | AAATGTGATTGTGGC[-/T]TCACAGAGCACTCGC | 317 |
rs776870902 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684442 | CTTCCCTTCCTCTTG[A/T]CCTTCCTTTCTCTCC | 317 |
rs776940896 | snp | C/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733591 | GCACGAGCCACCACA[C/G]CCAGCTAATTTTTAA | 317 |
rs776953955 | snp | A/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643456 | TTAAGATGCCAATCT[A/T]ATTAAAATGAAATGG | 317 |
rs776973655 | snp | A/G/T | 7.95614e-05 | 0.00630676 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644616 | CTCCGGGCCACGGGG[A/G/T]TCTTCCCGCCCTCGC | 317 |
rs776987794 | snp | C/T | 1.77303e-05 | 0.00297739 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644678 | CTTGGGCCCCGACTT[C/T]TTCCGGCTCTTCACC | 317 |
rs777008679 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659432 | ACATCATGCCTTTTT[C/T]CTGCTGTTCTATAGG | 317 |
rs777010088 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726174 | TAGAAAACAATCTAT[G/T]TTTTTTAGATATATA | 317 |
rs777013051 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732400 | CCAATCTAATGAGAA[C/T]TTTATTTTTCTCTGA | 317 |
rs777017529 | snp | C/T | 1.65138e-05 | 0.00287343 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665710 | AGCCATGTCTATAAG[C/T]GTTGAAATGCTCAGA | 317 |
rs777035808 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655950 | ACCACACCCAGCTAA[-/T]TTTTTTGTATTTTTA | 317 |
rs777043106 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717085 | ATGCTGGCCAGGCTG[C/G]TCTTGAACTCCTGAC | 317 |
rs777048128 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724624 | CAGCTCTTCTGAAGC[A/G]TTTCCTGACCCTCAA | 317 |
rs777048830 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697452 | GTGTTTAATAAATGT[C/G]TTAAAGATGATAAAC | 317 |
rs777052715 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703409 | CCTATTGGGAGAAAT[C/T]CACACGGGCCATCAC | 317 |
rs777052879 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671606 | TGGACGACAGCCATT[C/T]CCTAATATTGTACAA | 317 |
rs777059545 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710288 | TACAGCTTGAGTTAA[C/T]TTTTTCCATATGGGT | 317 |
rs777065914 | snp | C/G | 1.64953e-05 | 0.00287182 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712335 | TCATTAATGGAAGAA[C/G]AGGTCAGATTGATTA | 317 |
rs777070756 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689400 | ATATTTTTTAATGCC[C/T]GTCAAAACTTTAGGC | 317 |
rs777105871 | snp | A/G | 3.29652e-05 | 0.00405974 | splice-donor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98671720 | TTACCTGGAATGGAT[A/G]TAAGTAGGTTAGGAG | 317 |
rs777119808 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707192 | TACTTCTGTTTCTGC[C/T]ATTAAGCTTCTCCAC | 317 |
rs777125322 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727680 | GCACGGTGGCTCACG[-/C]CTGTAATCCTAGCAC | 317 |
rs777155570 | snp | A/C/T | 3.30645e-05 | 0.00406588 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665593 | TGGTGCACTTTTACG[A/C/T]GATTTTCCCAATCGC | 317 |
rs777158081 | in-del | -/ATG | 7.17052e-05 | 0.00598727 | downstream-variant-500B, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735542 | GGCTTTATCAGCTAT[-/ATG]ATGTAAATTCAATTC | 317 |
rs777209455 | in-del | -/TTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664007 | AGTTTTGTTTGTTTA[-/TTTA]TTTATTTATTTATTT | 317 |
rs777293241 | snp | C/T | 3.29739e-05 | 0.00406028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671538 | GTTTATTTGTAGGAT[C/T]GTGCAGTCAGTGAGA | 317 |
rs777307024 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716732 | GAAGTTGAATTATTT[A/C]TTTGATTCTTTCCTT | 317 |
rs777309249 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657162 | GTTGAGCATTCTCTT[C/G]TACTCTTTACCCACC | 317 |
rs777352704 | snp | A/G/T | 6.5933e-05 | 0.00574132 | synonymous-codon, missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699539 | TGCTGATGGTGCAAG[A/G/T]ATAATGGTGGCAGCA | 317 |
rs777403695 | snp | C/T | 1.65132e-05 | 0.00287339 | intron-variant | APAF1 | GRCh38.p7 | 12:98703333 | GCTTATCTCTTAAAG[C/T]ATTTTACCTTCATAG | 317 |
rs777404206 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683807 | ACAAATGAGTGAGGT[C/T]AACTCTACTTGAATC | 317 |
rs777419896 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694520 | TTTCTTTAGCTTTAC[-/T]TTTCTTTCCTTCTAT | 317 |
rs777446636 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702222 | AGGCACCTGCCACCG[C/T]GCCCGGCTAATTTTT | 317 |
rs777529217 | snp | A/G | 6.58913e-05 | 0.00573945 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671660 | TTCAGAAGTTTATCA[A/G]CAAGCTAAGCTGCAG | 317 |
rs777531131 | snp | C/G | 6.76235e-05 | 0.0058144 | intron-variant | APAF1 | GRCh38.p7 | 12:98671100 | AGGTATATATATTAA[C/G]ATGAAAAATTAGTGC | 317 |
rs777544649 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705937 | AGAAGTCTTGCTTTC[A/G]TCCCTATCCCTTCGC | 317 |
rs777545846 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720224 | GGAAGAATAATTTCT[A/G]GAGATATTTTTAGAA | 317 |
rs777653290 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686129 | ATTCTCAAAACATGC[A/G]TTTCTATCATGTTTG | 317 |
rs777675629 | snp | C/G | 1.66087e-05 | 0.00288168 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665553 | ATTTTTTTTTTAAAG[C/G]CTCTCCCCTTGTAGT | 317 |
rs777683848 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661117 | CGTGTTAACCAGGAT[A/G]GTCTTGATCTCCTGA | 317 |
rs777684491 | snp | C/G | 1.66452e-05 | 0.00288484 | intron-variant | APAF1 | GRCh38.p7 | 12:98727354 | GAAAGAAAATAATAG[C/G]CTATATCATACTTTC | 317 |
rs777766184 | in-del | -/TTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98686718 | ACTCAATACTAGTTG[-/TTTA]TTTATCTTTTTTTCT | 317 |
rs777773906 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690065 | TTTTCTAGGAAAATA[C/T]TTAAATACTCCTGGG | 317 |
rs777784600 | in-del | -/TT | 1.6476e-05 | 0.00287014 | intron-variant | APAF1 | GRCh38.p7 | 12:98715573 | AGGGAGGATGAACTC[-/TT]AACATATTTAATGCT | 317 |
rs777800292 | snp | G/T | 3.30284e-05 | 0.00406363 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648731 | CATGAAGGATATAAA[G/T]ATCTTGCTGCCCTTC | 317 |
rs777805227 | snp | C/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725457 | CTTCATGAATTGAGG[C/G]GCCACAACGGCTGTG | 317 |
rs777810915 | snp | A/C | 1.65806e-05 | 0.00287924 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732489 | AATCTTAAGAAAATA[A/C]ACGTGTCCCCTGACT | 317 |
rs777873748 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727461 | CTAAGGTGGGAGGAT[C/T]GCTGGAGTCTGTGAG | 317 |
rs777874229 | in-del | -/G | 1.6473e-05 | 0.00286988 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725479 | ACGGCTGTGTGCGCT[-/G]CTCTGCCTTCTCTGT | 317 |
rs777903794 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690478 | TGGTTTTTACTCAGT[A/G]AAAGACTTCAGAAGA | 317 |
rs777921326 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698596 | GAGATTTGAAAATGT[A/G]CCTGGCCAGAAAAAT | 317 |
rs777960598 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709423 | AATGGTATTCAGGAG[C/T]TCGGAGTGGTGGTAA | 317 |
rs777960954 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671032 | AACAGAACTTGTAGG[C/T]CCTGCTCATCTGATT | 317 |
rs777964396 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709910 | TGAGACAGTTTCTCT[C/G]TGTTGCCTAGGCTGG | 317 |
rs777981927 | snp | A/T | 1.64882e-05 | 0.00287121 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727176 | ATGTTTATGTAGATA[A/T]GGAATGTCTCAAACG | 317 |
rs777992532 | snp | A/T | 1.65562e-05 | 0.00287712 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708641 | GTTAAAGCAAGAAGT[A/T]GATGTTGTGTTTCAA | 317 |
rs778035063 | in-del | -/GG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717565 | ATATTTAGTAGAGAT[-/GG]GGTTTCTTCATGTTG | 317 |
rs778044060 | snp | A/G | 8.42779e-05 | 0.00649091 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98680370 | ACAGATGACAGATTT[A/G]TAGCAACCTGCTCAG | 317 |
rs778049714 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677406 | TTTAATTTCTGTTCA[-/T]TTTTTTCCCTGTATT | 317 |
rs778075105 | snp | C/T | 3.55114e-05 | 0.0042136 | intron-variant | APAF1 | GRCh38.p7 | 12:98662610 | TACCTTTATATTTAA[C/T]TTAATTACATTTAAA | 317 |
rs778129494 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689264 | CCCTATACCTTAATT[G/T]TCTGTTCTGGGCAAG | 317 |
rs778171239 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703077 | GGAGAACTACTCTGT[A/G]TGTTAATTGGGCCAG | 317 |
rs778174295 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688471 | CCACTGTTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 317 |
rs778242420 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720124 | GAAGTTCTTTTGAGA[C/T]ATTGTATACTATGTA | 317 |
rs778307064 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723201 | TATTCAGGTATGGAA[C/T]TGGCAATTGGACAAA | 317 |
rs778322898 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98725723 | CTGCAGAAACGGATT[C/T]ATTTTAGAGTTAGAG | 317 |
rs778325329 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651924 | GGCTCAAGTGATCTT[A/C]CCACCTCAGCCTCCG | 317 |
rs778329235 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664519 | AAGTTGAGATTATGT[A/G]TATGTGGTTTTGGAT | 317 |
rs778379007 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669136 | ATAAATACTTGTGCC[C/G]TAATTTACTTAACCA | 317 |
rs778406212 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98717205 | GTTTTCCTCAGTTTT[G/T]CCTTCCAGCCATTTT | 317 |
rs778433753 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671293 | CTAGGAAAATAAGAT[A/G]TTCAGTGGTTTTTTT | 317 |
rs778449956 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666238 | GAAGTTGAAGACATA[C/T]TGCAGGAGTTTGTAA | 317 |
rs778457530 | snp | C/G | 3.29908e-05 | 0.00406132 | intron-variant | APAF1 | GRCh38.p7 | 12:98703353 | TACCTTCATAGGTAT[C/G]TCTATTTATGTTGAC | 317 |
rs778485671 | snp | C/T | 1.66045e-05 | 0.00288132 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732493 | TTAAGAAAATACACG[C/T]GTCCCCTGACTTCAA | 317 |
rs778498609 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659301 | TTAATATTGAAGAGG[A/C]TAAAGACCGTCTCCG | 317 |
rs778499033 | snp | C/G | 2.62974e-05 | 0.00362602 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644575 | TCAGGCACGTTCGGG[C/G]GTCTGCCCAGCCCCC | 317 |
rs778525244 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704936 | AGGTGCCCACCAGCA[G/T]GCCCGGCTAATTTTT | 317 |
rs778544251 | snp | A/G | 1.74775e-05 | 0.00295608 | intron-variant | APAF1 | GRCh38.p7 | 12:98677381 | AAAATAGTTACTTTT[A/G]CTCTCATTTATTTAA | 317 |
rs778544930 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697246 | TACCTCCTGTACAAA[A/G]TGTTCCCTCAAGCCC | 317 |
rs778546488 | snp | A/G | 1.6574e-05 | 0.00287867 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665567 | GGCTCTCCCCTTGTA[A/G]TATCTTTAATTGGTG | 317 |
rs778567480 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660486 | TTCAACAGTTAATTA[A/G]TTCAGCAAATACTTA | 317 |
rs778576678 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705863 | TGGATTGACTTTTTT[A/G]AAGTGATAAAATATT | 317 |
rs778619034 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734300 | AGCTTTTGACAGGGG[A/G]AAAAACTCAATAACT | 317 |
rs778622726 | in-del | -/T | 1.65641e-05 | 0.00287781 | intron-variant | APAF1 | GRCh38.p7 | 12:98727141 | GCTTCTGGATAACTC[-/T]TGTTAATGAATTGTG | 317 |
rs778632030 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696420 | AGGCATTAGAAGGCA[-/T]TCATCTGTTTATGAG | 317 |
rs778635647 | in-del | -/TTCA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704299 | CAGGCTTTCTTAGTC[-/TTCA]TTCATTCCTTAGGTT | 317 |
rs778654991 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98676841 | GTAGAGACGGTGTTT[C/T]GCCATGTTGGCCAGG | 317 |
rs778671229 | snp | G/T | 3.30175e-05 | 0.00406296 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665671 | AAGGAAATCTTCGTC[G/T]TATGATTATGAGGCT | 317 |
rs778720170 | in-del | -/A | | | | | GRCh38.p7 | 12:98706244 | TTCCATTATGTGATT[-/A]AATGTAGTTTATTCA | 317 |
rs778721405 | snp | C/T | | | | | GRCh38.p7 | 12:98648154 | AGTGCATAAGAATGG[C/T]CATTTTCTCATACCT | 317 |
rs778771599 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709615 | TGGAAGATTAAAACA[C/T]AAGAGGCTATCTATA | 317 |
rs778794795 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698502 | TTTGCATTACCCAGA[C/T]TACCTGCAGTTGTTG | 317 |
rs778819519 | snp | A/T | 1.8936e-05 | 0.00307695 | intron-variant | APAF1 | GRCh38.p7 | 12:98715382 | GTGTAATGCCTATGT[A/T]TTGCTTAGTTTCTTC | 317 |
rs778853424 | snp | C/T | 3.43e-05 | 0.00414112 | intron-variant | APAF1 | GRCh38.p7 | 12:98662628 | AATTACATTTAAATA[C/T]GTGACATACCAAATT | 317 |
rs778908657 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648457 | ACATGATTAGTGATG[C/G]ATTTTTAACAATATC | 317 |
rs778918980 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651829 | TGGCTAATTATTTAT[G/T]TATGAAACAGGGTCT | 317 |
rs778936197 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659082 | TAAATTGGAGTAAAT[C/G]TGATGCTTAACAGTA | 317 |
rs778942552 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | APAF1 | GRCh38.p7 | 12:98683304 | TGAGAATTAGGTAGA[C/T]AAATTTGATTCGTAC | 317 |
rs778943117 | snp | A/G | 9.88712e-05 | 0.00703035 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727191 | TGGAATGTCTCAAAC[A/G]GTGAGCTTCTTCATT | 317 |
rs778991920 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728011 | AATAAAAAGGAAAAG[-/A]AAAAAAAAGGCAGTT | 317 |
rs778995599 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686819 | AGTCAATCACTGCAG[A/G]TTTTCACCAGATGAT | 317 |
rs779010907 | in-del | -/TTG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719369 | TTTCTTTTCTTTTTT[-/TTG]AGACAGTCTTGCTCT | 317 |
rs779069813 | snp | A/C | 1.65982e-05 | 0.00288077 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708656 | AGATGTTGTGTTTCA[A/C]GAAAATGAAGTGATG | 317 |
rs779079030 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675150 | AAAGAATGCTTTATT[G/T]AAGTACTAGAAACTT | 317 |
rs779083325 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723922 | GCATTTAGTTGGTAT[C/G]AAATGAATGAAATGA | 317 |
rs779144426 | snp | A/G | 6.61463e-05 | 0.00575055 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683155 | TAGATTTGGAATTCT[A/G]TGACTGGGGAACTAG | 317 |
rs779162481 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716806 | GATGTTAGATCTCCC[A/G]GACTGATAATCTAGT | 317 |
rs779176654 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702948 | AATTTGGTAGTTCTA[C/G]AGAGAAATAAAAATG | 317 |
rs779183383 | snp | A/G | 8.34829e-05 | 0.00646022 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662763 | TAATATGAAGAAGGC[A/G]GATTTGCCAGAACAA | 317 |
rs779196602 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651759 | CAAACTTTTAGGCTC[A/G]AGTGATCCTCCCACC | 317 |
rs779199907 | in-del | -/G | 1.64808e-05 | 0.00287057 | frameshift-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662512 | TGAAAGCTTTTGACA[-/G]TCAGTGTCAGATTCT | 317 |
rs779212954 | snp | A/C/T | 3.38102e-05 | 0.00411147 | splice-donor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98680404 | ATAAAAAAGTGAAGG[A/C/T]AGGAAAATCTTTTCC | 317 |
rs779225119 | snp | C/G | 1.66322e-05 | 0.00288371 | intron-variant | APAF1 | GRCh38.p7 | 12:98648580 | CCACTACTTTATGTT[C/G]CATACATATTCATTG | 317 |
rs779226780 | in-del | -/A | 1.69289e-05 | 0.00290933 | intron-variant | APAF1 | GRCh38.p7 | 12:98723615 | AAAGTGTCAACCTCC[-/A]AGTGTTTTTTTTTTT | 317 |
rs779232554 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710141 | GCCTCCCAAAGAGCT[-/G]GGGATTATAGGTGTG | 317 |
rs779246349 | snp | G/T | 5.03453e-05 | 0.00501698 | intron-variant | APAF1 | GRCh38.p7 | 12:98723625 | CCTCCAAGTGTTTTT[G/T]TTTTTTTTTTAAGGT | 317 |
rs779280928 | snp | A/G | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729802 | TGCAATTTTACCACC[A/G]TAAGAATCTAGCTTA | 317 |
rs779299447 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699555 | ATAATGGTGGCAGCA[A/G]AAAATAAAATCTTTG | 317 |
rs779402537 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680921 | ATTCCTGTTGTAAGA[C/T]ACAATTTTAAAATGC | 317 |
rs779406623 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664926 | CATAATATTGATATA[C/T]CTTAATTTATTCAAC | 317 |
rs779406967 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695857 | CACCTTTATCAGAAG[C/G]TACTGGGTGCCAGCA | 317 |
rs779418235 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726896 | TCTTGGATTTTCTAG[G/T]GAGAGATTTACAAAT | 317 |
rs779479872 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | APAF1 | GRCh38.p7 | 12:98677560 | CTTACAGGTAAAACA[C/T]ATCTCTTGAGAAAAA | 317 |
rs779520346 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731269 | CATTATGAACATCCC[C/T]CCACCAGAGATGTGC | 317 |
rs779532810 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723743 | CAAGTTTTCATCTAC[C/T]TCTGCTGACAAGACT | 317 |
rs779559276 | snp | A/C/G | 3.5569e-05 | 0.00421704 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644733 | ACGACAAGCCCAGGG[A/C/G]AGCTTCTTCACCAGG | 317 |
rs779571995 | in-del | -/A | 4.97876e-05 | 0.00498912 | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677428 | CCTGTATTTAGAAAC[-/A]AAAAAAAACATCACG | 317 |
rs779574454 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98683475 | GTCTAGAGGGAGCAT[G/T]GCTTCAGGCATAGCT | 317 |
rs779594536 | snp | C/T | 3.32618e-05 | 0.00407797 | intron-variant | APAF1 | GRCh38.p7 | 12:98665809 | AATGGGATCAATGAT[C/T]CTCATCATTGGGTAT | 317 |
rs779614230 | snp | A/G | 8.65029e-05 | 0.00657602 | intron-variant | APAF1 | GRCh38.p7 | 12:98677391 | CTTTTACTCTCATTT[A/G]TTTAATTTCTGTTCA | 317 |
rs779653660 | snp | A/T | 3.30158e-05 | 0.00406286 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665678 | TCTTCGTCTTATGAT[A/T]ATGAGGCTCTAGATG | 317 |
rs779665888 | in-del | -/TTTTT | 1.76382e-05 | 0.00296965 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665539 | AGCATAGTGACTTCA[-/TTTTT]TTTTTAAAGGCTCTC | 317 |
rs779703679 | snp | G/T | 1.7047e-05 | 0.00291945 | intron-variant | APAF1 | GRCh38.p7 | 12:98648880 | GTTTGTCTTATTGTA[G/T]ATGTAATCTTTTGAA | 317 |
rs779714415 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718398 | CCATCACATGCAGCT[A/G]ATTTTTTTGTATTTT | 317 |
rs779750674 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681322 | CTGCCTTTGACTCCC[A/G]AAGTGCTGAGATTAT | 317 |
rs779750826 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697045 | TTCACATACCTGATA[C/T]TACAACCAGATTGAA | 317 |
rs779756742 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649491 | TTGGATTTTAGTAAG[A/G]ACAGTCCTGTGTGAA | 317 |
rs779793240 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688892 | TGATCCTGGCCCACC[A/G]CAGTCTATCTCCTGG | 317 |
rs779804867 | snp | A/G | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643567 | ACGAGTTGGTTTTAA[A/G]GTTATTTCTAATATT | 317 |
rs779838528 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696198 | CATGATTCTGATGGC[C/T]GGAAATTCCAGGATT | 317 |
rs779872265 | snp | C/G | 1.64942e-05 | 0.00287173 | intron-variant | APAF1 | GRCh38.p7 | 12:98723155 | AATGAGATAGGATCG[C/G]GGGAGGATTATAACA | 317 |
rs779903658 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723433 | TTTTAATTTTTCTCA[A/T]GCTTGTTTTCTGTTA | 317 |
rs779926398 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667375 | CCTACCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 317 |
rs779960308 | in-del | -/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646521 | AAGTTACTTGTGCTC[-/T]TGTTTTTGCACTTCG | 317 |
rs779968101 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686846 | TGATAAGCTTTTGGC[C/T]AGTTGTTCAGCTGAT | 317 |
rs779969240 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant | APAF1 | GRCh38.p7 | 12:98712286 | AAACTGCTCTTACAG[C/T]CTAATAACTGATTTT | 317 |
rs779982484 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98675004 | GTTTAGTTCTTGTTC[G/T]CTTATGAATTGTTGA | 317 |
rs779984143 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98657523 | GTCACTTCAAGTTAT[A/G]AAAAGTCTAATTTTC | 317 |
rs779994121 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647705 | GGGATCATGTTTCTG[-/T]TTTTTTTTTTTTTTT | 317 |
rs780035318 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658862 | AAGGTTTAGAAACTG[C/T]GCTGTGCAGTGATCA | 317 |
rs780052398 | in-del | -/TTTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672173 | TTATTTATTTATTTA[-/TTTA]TTTATTTTTGAGACA | 317 |
rs780082497 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664391 | TACAAAGGGTGATGC[A/G]TGTCCATTTTGAAAA | 317 |
rs780153425 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701659 | TTCTAGTGAGAGGAA[A/G]ATAATTTTATATTGC | 317 |
rs780176134 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98665953 | GTTAGCTTCCATTAA[C/G]GGCTTTGTGTTGAAC | 317 |
rs780185808 | in-del | -/AGA | 1.64746e-05 | 0.00287002 | cds-indel, intron-variant, splice-acceptor-variant | APAF1 | GRCh38.p7 | 12:98727223 | GTGTGCTCCGCTTTC[-/AGA]AGAAGGAGCTGCTAC | 317 |
rs780203359 | snp | A/T | 1.64901e-05 | 0.00287137 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683166 | TTCTATGACTGGGGA[A/T]CTAGTACACACCTAT | 317 |
rs780207328 | in-del | -/GAT | | | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735918 | TGTACAGACCTGAAA[-/GAT]GATGTGAGGAAGTGA | 317 |
rs780217391 | snp | C/T | 5.00121e-05 | 0.00500035 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665534 | GTATTAGCATAGTGA[C/T]TTCATTTTTTTTTTA | 317 |
rs780217415 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant | APAF1 | GRCh38.p7 | 12:98648589 | TATGTTGCATACATA[C/T]TCATTGTTGTATACT | 317 |
rs780260260 | snp | C/T | 1.6519e-05 | 0.00287388 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666355 | AATTGCAGCCAGCTT[C/T]AGGTACTTGCATCTT | 317 |
rs780260375 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683271 | AAGTGACTGCTTCCT[C/T]AAAGTAAGTGTGGAT | 317 |
rs780316558 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98679172 | CTTCTGAAGCCCATA[A/C]AAGCCTCGGGCTTAG | 317 |
rs780332778 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659310 | AAGAGGCTAAAGACC[A/G]TCTCCGCATTCTGAT | 317 |
rs780364276 | in-del | -/CC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724735 | CTAACTGTTCGTGAG[-/CC]TGTCTTTGTGATTAA | 317 |
rs780399310 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98713207 | TATCCAGTTGGCTGT[A/G]TATTTTTCAGATTTC | 317 |
rs780459323 | snp | A/G | 7.12657e-05 | 0.0059689 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644666 | AGCAGGGGCTCCCTT[A/G]GGCCCCGACTTCTTC | 317 |
rs780544831 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723756 | ACCTCTGCTGACAAG[A/G]CTGCAAAGGTAGGTC | 317 |
rs780545365 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696048 | CCTTGTGGATTATGC[C/T]GAGAGAAAAATTCCT | 317 |
rs780548843 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98694041 | GAGAGGACTCTCTAT[G/T]CAATAAATGGTGCTG | 317 |
rs780564438 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700155 | ATTTGTGGTATTCAG[A/C]GTGCCCTCACATATA | 317 |
rs780565840 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658809 | CATAGGACAGTCCCT[G/T]ACAACAAAGAATTGC | 317 |
rs780615265 | in-del | -/AG | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733159 | TTTGTTTTTGGAGAC[-/AG]AGTCTTGCTTTGTTG | 317 |
rs780618856 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666223 | GACATGGAAACTGAA[A/G]AAGTTGAAGACATAC | 317 |
rs780628408 | snp | A/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643440 | ATGGAGAAAAATTCT[A/T]TTAAGATGCCAATCT | 317 |
rs780661111 | snp | C/T | 3.51525e-05 | 0.00419225 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735662 | GAATTCATTTATTTA[C/T]TCACTTAGTTTGTTC | 317 |
rs780671464 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703397 | TCATACTAGTGGCCT[A/G]TTGGGAGAAATCCAC | 317 |
rs780671548 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | APAF1 | GRCh38.p7 | 12:98725411 | AATCCTAATTGCCTT[C/T]CAGATCTGGAGTTTT | 317 |
rs780720806 | snp | C/T | 9.88517e-05 | 0.00702966 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703451 | GTACTGTGACTTCTC[C/T]CCACAAAACCATTTG | 317 |
rs780723168 | snp | A/G | 1.65438e-05 | 0.00287605 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699439 | CAGCAAATGAGAGGA[A/G]AAGCATTAATGTGAA | 317 |
rs780750349 | snp | C/T | 1.66474e-05 | 0.00288503 | intron-variant | APAF1 | GRCh38.p7 | 12:98665817 | CAATGATCCTCATCA[C/T]TGGGTATTTATTGCA | 317 |
rs780785542 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | APAF1 | GRCh38.p7 | 12:98723172 | GGAGGATTATAACAG[A/G]CTTATTTCTTTGATA | 317 |
rs780803533 | snp | G/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649502 | TAAGGACAGTCCTGT[G/T]TGAAGGTGGAGTACC | 317 |
rs780804274 | snp | C/T | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731296 | GTGCATTTGTTACAA[C/T]TGATGGATCCACATT | 317 |
rs780832700 | snp | A/G | 1.69226e-05 | 0.00290878 | intron-variant | APAF1 | GRCh38.p7 | 12:98723609 | TTCTTAAAAGTGTCA[A/G]CCTCCAAGTGTTTTT | 317 |
rs780833686 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672032 | TTGGAGCCACAGAAC[C/T]GGGTTTGAGCCTCAG | 317 |
rs780845725 | snp | A/G | 1.65195e-05 | 0.00287393 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671067 | AATTTGTGGAATACA[A/G]ACATATACTAGATGA | 317 |
rs780889932 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708241 | TGAGCCCCTGCGCCT[A/G]GCCCAAACTTCTTAC | 317 |
rs780894384 | in-del | -/G | 1.80083e-05 | 0.00300064 | intron-variant | APAF1 | GRCh38.p7 | 12:98708729 | TTTTAGAAAACAATT[-/G]GAAAATTGTTTTGGT | 317 |
rs780929796 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712760 | TTTAAGCGATTGTCC[A/G]GCCTCAGCCTCCCAA | 317 |
rs780941504 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98696381 | GAGAACTAATCCATT[-/C]CCAGGGAACTCACCC | 317 |
rs780969177 | in-del | -/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98662344 | CTAGCCATCTATTTG[-/TTT]TAAAAAAAATTTAAT | 317 |
rs780979961 | snp | A/C/T | 8.24836e-05 | 0.00642151 | intron-variant | APAF1 | GRCh38.p7 | 12:98723147 | ACCCCTCCAATGAGA[A/C/T]AGGATCGGGGGAGGA | 317 |
rs780981578 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707336 | CTTAAGTGGTTTCTT[A/T]TATTTGGAATGCTCT | 317 |
rs781059713 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648557 | AATTTCAGAACTTGT[A/T]CTGGTCTCCACTACT | 317 |
rs781078640 | snp | C/T | 1.66988e-05 | 0.00288949 | intron-variant | APAF1 | GRCh38.p7 | 12:98648842 | TTATACCTTCTATCA[C/T]TTTGCTATCAAAATT | 317 |
rs781095784 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653005 | AGTAGACGAGAACTC[-/T]TGATGTAGTCAAACT | 317 |
rs781120511 | snp | C/G | 4.94214e-05 | 0.00497074 | missense, intron-variant | APAF1 | GRCh38.p7 | 12:98727213 | TTCTTCATTTGTGTG[C/G]TCCGCTTTCAGAAGA | 317 |
rs781127726 | snp | A/G | 3.29473e-05 | 0.00405864 | intron-variant | APAF1 | GRCh38.p7 | 12:98683298 | GGATATTGAGAATTA[A/G]GTAGATAAATTTGAT | 317 |
rs781215041 | in-del | -/ACA | 4.94499e-05 | 0.00497217 | intron-variant | APAF1 | GRCh38.p7 | 12:98677559 | CCTTACAGGTAAAAC[-/ACA]TCTCTTGAGAAAAAT | 317 |
rs781228664 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689570 | ACTAAAGTGATCCTC[C/T]TGCCTCAACCGCCTG | 317 |
rs781292200 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664232 | TCATCTTGGCCAGGG[C/T]AGTCTTGAACTCCTG | 317 |
rs781296082 | snp | A/T | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667536 | TAAGAAGATAATCAC[A/T]CAGTTTCAGAGATAT | 317 |
rs781301099 | snp | A/G | 1.68926e-05 | 0.0029062 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662796 | TCATAGTATTATAAA[A/G]GAATGTAAAGGTATG | 317 |
rs781375405 | snp | A/G | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646816 | AAAGTTGCTAGAAAC[A/G]TCAAGTATTTTACTA | 317 |
rs781378235 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | APAF1 | GRCh38.p7 | 12:98725543 | TGGAGAAATCAGGGT[A/G]GGCTGTTTGCTGACA | 317 |
rs781388890 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698780 | GAGGAGTGAAGGTGG[A/T]TCTTCTTGAAGGCCT | 317 |
rs781420888 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667639 | GCCAGTGCCAAGATG[C/T]ACAAGGTAAGATGAC | 317 |
rs781435330 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692547 | GGTGCCTCATTCCCC[A/C]CTCCCCAACTCTAGT | 317 |
rs781444065 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98699704 | TCTTCCTAACCTGTC[A/G]TGGTTCTTTGGAACT | 317 |
rs781466059 | snp | A/G | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648650 | CAGCAAAGAGCAGCT[A/G]TGCTGATTAAAATGA | 317 |
rs781471884 | snp | A/T | 5.02685e-05 | 0.00501316 | intron-variant | APAF1 | GRCh38.p7 | 12:98662449 | TAATATTTTTTTTTT[A/T]AATTAGGTCTCTCTT | 317 |
rs781472134 | snp | A/T | 3.55948e-05 | 0.00421855 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644741 | CCCAGGGCAGCTTCT[A/T]CACCAGGGGGAGCAG | 317 |
rs781561654 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98677201 | TTGTAACACGTGACA[A/G]GTTGCTTGATAAAGG | 317 |
rs781574920 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98660789 | TGGCTCTGCACTTTT[A/T]AAAAATGCCCTAATG | 317 |
rs781618438 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653422 | AGCACTCTGGGAGGC[C/G]GAGGTGGACAGATCA | 317 |
rs781643760 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648431 | CATCAAGACATCCTA[C/T]ATCATGGATCACATG | 317 |
rs781655092 | in-del | -/C | 2.08753e-05 | 0.00323067 | upstream-variant-2KB, frameshift-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644608 | CTCCGCTGCTCCGGG[-/C]CACGGGGGTCTTCCC | 317 |
rs781661345 | snp | C/T | 6.58968e-05 | 0.00573969 | intron-variant | APAF1 | GRCh38.p7 | 12:98703509 | GTAGAGGTGAGTAGT[C/T]GAATTTATTCTGTGA | 317 |
rs781661564 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98705569 | CTGAAATGATAAAGT[A/G]GTTCTGTAATTTAAA | 317 |
rs781682684 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668775 | GAATGGGGATGGTTA[A/G]GAACTCATTTTGGAT | 317 |
rs781687687 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673977 | TTTTTTAAGTTAAAA[A/T]GTTTAATTTTTGTTG | 317 |
rs781779128 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704592 | GGCATGAGATCCATA[A/G]GCTTCTCCTAATTCT | 317 |
rs796099496 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707693 | CATTATGCAAAGTAC[-/TA]TATATATATATATAT | 317 |
rs796119016 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673442 | CTCTGTCTCAAAAAA[A/C]AAAAAAAAAAAAAAC | 317 |
rs796183480 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719362 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTGAGACAG | 317 |
rs796192646 | in-del | -/TC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674440 | CTTGTGAAGTGGAGG[-/TC]TCTCTCTCTCTCTCT | 317 |
rs796198821 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695389 | TGAGACAGGGTCTCA[-/CT]CTGTCACACAGGCTG | 317 |
rs796229067 | in-del | -/TC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688646 | GGCGAAATTTTTTTT[-/TC]TTTTTTTTTTTTTTA | 317 |
rs796295821 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98728563 | CATCTCTGCTAAAAA[-/A]TACAAAAATTAGCTG | 317 |
rs796432759 | in-del | -/TAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693690 | TCTGGTCGGTAATGG[-/TAA]TAATACTATTCCCAG | 317 |
rs796522892 | in-del | -/ATAAAC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682857 | CCTGCTTTCATTCAT[-/ATAAAC]ATAAACATGTGAAAT | 317 |
rs796606583 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724904 | TGAAAGAAAAAAAAA[-/A]TAGCATTTGGCTGCC | 317 |
rs796652982 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707570 | TTGACGTATCTTACA[-/T]TATAAGCTCTTTGAG | 317 |
rs796698474 | in-del | -/AC | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689505 | GTGTGTGAGAGAGAG[-/AC]ACAGGGTCTTACTTT | 317 |
rs796703094 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688645 | CTGGCGAAATTTTTT[C/T]TTTTTTTTTTTTTTT | 317 |
rs796763418 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727563 | AAAAAAAAAAAAAAA[-/A]TCTGGCAGTAAAATG | 317 |
rs796807068 | in-del | -/TGTG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689474 | GAGAGTGTGTGTGTC[-/TGTG]TGTGTGTGTGTGTGT | 317 |
rs796858804 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98667099 | TGGGGAGATTCTCTG[-/TA]TATATATATGTATTT | 317 |
rs796867355 | snp | A/T | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665274 | TATATATATATATAT[A/T]TATATTTTTTTTTTT | 317 |
rs796877002 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710962 | GAGTAGATACTGGGA[A/G]TAAATCGCCTGGTAT | 317 |
rs796912601 | in-del | -/GAGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689436 | CTTTTGTGTGAGGGT[-/GAGA]GAGAGAGAGAGAGAG | 317 |
rs797002314 | in-del | -/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666852 | GAGTACTTGGTGGTT[-/TTT]AAAAAATTTTTTGTA | 317 |
rs797004866 | in-del | -/AT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650910 | CTTTGTGTATTTATA[-/AT]ATTCCAATTTATAGG | 317 |