SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12159 | snp | A/T | 0 | 0 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735244 | TTCCCTTGCTGTATT[A/T]TTTTGTATTATAAAT | 317 |
rs919699 | snp | C/T | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98690548 | GCAGTCTTCCCAGAA[C/T]TTGGAATTAGCAAAG | 317 |
rs1007573 | snp | C/T | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98698843 | TGAGATACAAAATAC[C/T]GTAAACTTTGCTCAC | 317 |
rs1131019 | snp | A/G | | | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733572 | caagtagctgagact[A/G]caggcacgagccacc | 317 |
rs1131020 | snp | A/G | 0 | 0 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734993 | tggcacgtgcctgta[A/G]tcccagctccttggg | 317 |
rs1131021 | snp | A/G | 0 | 0 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735014 | gctccttgggaggct[A/G]agacaggaggattcc | 317 |
rs1148446 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727690 | gcctcccaaagtgct[A/G]ggattacaggcgtga | 317 |
rs1195707 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98672437 | tggctcatgcctgta[A/G]tcccagcactttggg | 317 |
rs1195708 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98672416 | gcactttgggaggcc[A/G]aggcatgcagctcac | 317 |
rs1201632 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98672390 | ctcacttgaaatcag[A/G]agtttgagaccagcc | 317 |
rs1209284 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98727678 | gctaggattacaggc[A/G]tgagccaccgtgcct | 317 |
rs1439122 | snp | A/G | 0.235273 | 0.249566 | intron-variant | APAF1 | GRCh38.p7 | 12:98682729 | ccctaacttacctgc[A/G]tctcagttccctctt | 317 |
rs1439123 | snp | C/T | 0.235273 | 0.249566 | intron-variant | APAF1 | GRCh38.p7 | 12:98682538 | cagctttcaacccta[C/T]tactgttcccagttt | 317 |
rs1439124 | snp | A/C | 0.25801 | 0.249872 | intron-variant | APAF1 | GRCh38.p7 | 12:98726292 | TTTTCCATAATTTCT[A/C]ATCTTTCAGCATGCA | 317 |
rs1566302 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98698770 | TCATGGCCCAGAGGA[A/G]TGAAGGTGGATCTTC | 317 |
rs1866477 | snp | A/C | 0.184521 | 0.241273 | intron-variant | APAF1 | GRCh38.p7 | 12:98726055 | GCCCTTCGCTGCCCC[A/C]CAATGACGGAAATGT | 317 |
rs2060175 | snp | A/G | 0.449853 | 0.150196 | intron-variant | APAF1 | GRCh38.p7 | 12:98719780 | AGCCCTACTAAAATG[A/G]CAAGATCAAAAGAAT | 317 |
rs2118851 | snp | C/G | 0.181022 | 0.240296 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645548 | GGCCGGGCCTCACCG[C/G]GGCGCTCCGGGACTG | 317 |
rs2118852 | snp | G/T | 0.180702 | 0.240204 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645689 | CGGACCTGCCCCGGG[G/T]CGAAGGGTATGTGGC | 317 |
rs2278361 | snp | C/T | 0.293807 | 0.246132 | intron-variant | APAF1 | GRCh38.p7 | 12:98649429 | GAATAATTACTGAAG[C/T]AATACCATAAAAAAC | 317 |
rs2288713 | snp | G/T | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98715645 | ATGCCCAACGTAATG[G/T]GTTTAAAATATACAC | 317 |
rs2288714 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | APAF1 | GRCh38.p7 | 12:98714510 | CTGATTTTATGAAAA[C/T]TGTGGAAATAAGAGT | 317 |
rs2288715 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | APAF1 | GRCh38.p7 | 12:98712664 | TCGGGCATGGTGACG[C/T]ACACCTTTAGTCCCA | 317 |
rs2288716 | snp | A/G | 0.474091 | 0.11083 | intron-variant | APAF1 | GRCh38.p7 | 12:98710643 | TGAGGCCAGGAGTTC[A/G]AGACCAGCGTGGTCA | 317 |
rs2288717 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | APAF1 | GRCh38.p7 | 12:98709998 | gtcccagctactcag[A/G]aggctcaggcatgag | 317 |
rs2288718 | snp | C/G | 0.0861826 | 0.188849 | intron-variant | APAF1 | GRCh38.p7 | 12:98705146 | TTGCTACTTAGTACT[C/G]TTTCTAAAAATCCTA | 317 |
rs2288719 | snp | A/C | 0.270621 | 0.249148 | intron-variant | APAF1 | GRCh38.p7 | 12:98704133 | CTATTAAAAAACAAA[A/C]AAAAAAAGCACTAAT | 317 |
rs2288720 | snp | C/T | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98703692 | GTCAAATCAAGTCTG[C/T]AATCACTGTTAAAAT | 317 |
rs2288721 | snp | C/T | 0.144296 | 0.226554 | intron-variant | APAF1 | GRCh38.p7 | 12:98700706 | AGTTTTGGAAATATA[C/T]AGTAGTAATGGCTAC | 317 |
rs2288722 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98698634 | AAGTCAGCTTCCAAA[G/T]CACAACTCCCAGGTA | 317 |
rs2288723 | snp | A/G | 0.269267 | 0.249256 | intron-variant | APAF1 | GRCh38.p7 | 12:98697561 | CTCATACATGAATAC[A/G]GAAATCAAAATCCTG | 317 |
rs2288724 | snp | G/T | 0.264906 | 0.249555 | intron-variant | APAF1 | GRCh38.p7 | 12:98691249 | GGAAAAGAAGGAAAG[G/T]GAGGAACAGTAGGTA | 317 |
rs2288725 | snp | G/T | 0.264906 | 0.249555 | intron-variant | APAF1 | GRCh38.p7 | 12:98691248 | GAAAAGAAGGAAAGG[G/T]AGGAACAGTAGGTAC | 317 |
rs2288726 | snp | G/T | 0.161924 | 0.233971 | intron-variant | APAF1 | GRCh38.p7 | 12:98690609 | TTTTACAGCTTTCTT[G/T]AACATTTGGCAACCT | 317 |
rs2288727 | snp | A/T | 0.269267 | 0.249256 | intron-variant | APAF1 | GRCh38.p7 | 12:98690021 | AAATTTACTGAATAC[A/T]TGAGTACAATTCTGT | 317 |
rs2288728 | snp | A/T | 0.207559 | 0.246371 | intron-variant | APAF1 | GRCh38.p7 | 12:98688717 | ATCCCAGCACTGGGA[A/T]TGCTTGAGCCCAGGA | 317 |
rs2288729 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | APAF1 | GRCh38.p7 | 12:98673812 | ATTGTAATTATTTGC[C/T]TAAACTCCTTTCTTC | 317 |
rs2288730 | snp | G/T | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98672736 | AAATAAAAATAAAAT[G/T]TACCTTATAAACTTG | 317 |
rs2288731 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | APAF1 | GRCh38.p7 | 12:98670065 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGGAAGGA | 317 |
rs2288732 | snp | C/T | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98668900 | TGTGCTAATAATTCC[C/T]TATTTTCATCTTTCA | 317 |
rs2288733 | snp | C/T | 0.237593 | 0.249692 | intron-variant | APAF1 | GRCh38.p7 | 12:98661109 | TCAAGACCATCCTGG[C/T]TAACACGGTGAAACC | 317 |
rs2288734 | snp | C/T | 0.192088 | 0.2432 | intron-variant | APAF1 | GRCh38.p7 | 12:98661093 | TAACACGGTGAAACC[C/T]CATCTCTACTAAAAA | 317 |
rs2288735 | snp | C/T | 0.192088 | 0.2432 | intron-variant | APAF1 | GRCh38.p7 | 12:98661092 | AACACGGTGAAACCT[C/T]ATCTCTACTAAAAAT | 317 |
rs2288736 | snp | A/G | 0.193028 | 0.243422 | intron-variant | APAF1 | GRCh38.p7 | 12:98661091 | ACACGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 317 |
rs2288737 | snp | A/G | 0.121022 | 0.21416 | intron-variant | APAF1 | GRCh38.p7 | 12:98651782 | cacccagctcctcag[A/G]aggctaaggtgggag | 317 |
rs2288738 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | APAF1 | GRCh38.p7 | 12:98651414 | AAAACAGAATAATAC[C/T]ATAACATCTATGCAA | 317 |
rs2288739 | snp | A/G | 0.185472 | 0.241529 | intron-variant | APAF1 | GRCh38.p7 | 12:98650985 | TTAATCCCTAGAATT[A/G]AAAATTCATCACAAT | 317 |
rs2289315 | snp | A/G | 0.0995161 | 0.199636 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644771 | GGACGTGGCCGCCTT[A/G]GCGTTCGTGGGAACC | 317 |
rs2289316 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644902 | CCAGCTCCATAGTTC[C/T]CCTAGGAGAGGTGGG | 317 |
rs2289317 | snp | A/C | 0.2462 | 0.249971 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644929 | TGGGCGGCGACCTCA[A/C]CCCACAGCGCCTTCC | 317 |
rs2304006 | snp | C/T | 0.27544 | 0.248702 | intron-variant | APAF1 | GRCh38.p7 | 12:98725562 | AAGAAGAGCAGTGCT[C/T]TCATGTCAGCAAACA | 317 |
rs2372445 | snp | C/T | 0.18134 | 0.240387 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665245 | tctcattatattgct[C/T]agactggCGCatata | 317 |
rs2840025 | snp | A/G | 0.269267 | 0.249256 | intron-variant | APAF1 | GRCh38.p7 | 12:98685111 | TGGCAAAAATTATTT[A/G]GAAATGATTAGTAAG | 317 |
rs2888315 | snp | A/G | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98693683 | TGCTCCATTCTGGTC[A/G]GTAATGGTAATACTA | 317 |
rs3214599 | in-del | -/T | 0.127944 | 0.218179 | intron-variant | APAF1 | GRCh38.p7 | 12:98715758 | TCAAAATAAACAACC[-/T]TCCAACAGAGGATTC | 317 |
rs3214600 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704152 | GGCAACACAGTGAGA[-/C]CCCCCATTTCTATTA | 317 |
rs3217367 | in-del | -/CAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691420 | GACAATTTTAAAGAA[-/CAA]TACAATCAAGGAAGA | 317 |
rs3217465 | in-del | -/AGCGCCTTCCAC | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644946 | CACAGCGCCTTCCAC[-/AGCGCCTTCCAC]TGCGATATTGCTCCA | 317 |
rs3782558 | snp | C/G | 0.49928 | 0.018956 | intron-variant | APAF1 | GRCh38.p7 | 12:98712015 | AGAAATGGTGTGGAG[C/G]TAGCTGTGGGATTAC | 317 |
rs3782560 | snp | C/T | 0.206029 | 0.246103 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731134 | CTTTGTGACCTTGCA[C/T]AAGATTGTTTAACTT | 317 |
rs3815997 | snp | A/G | 0.264358 | 0.249587 | intron-variant | APAF1 | GRCh38.p7 | 12:98677245 | AAGAAAAAAAATAAC[A/G]AAAGTAGCATTTGTA | 317 |
rs3825264 | snp | A/G | 0.206029 | 0.246103 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730962 | TTCACATTAATTCAT[A/G]TGCATGAAGGGAAAG | 317 |
rs3834481 | in-del | -/T | 0.0410182 | 0.13721 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735248 | CTTGCTGTATTWTTT[-/T]GTATTATAAATTACA | 317 |
rs4319556 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | APAF1 | GRCh38.p7 | 12:98682808 | CCCTTCTGACCAGAA[A/G]TCTATTATGCTAACC | 317 |
rs4341587 | snp | C/T | 0.221737 | 0.248397 | intron-variant | APAF1 | GRCh38.p7 | 12:98693809 | TTTTTTTTTTTTTTT[C/T]GTCTTCTTTCTTGGC | 317 |
rs4403844 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | APAF1 | GRCh38.p7 | 12:98682811 | TTCTGACCAGAAATC[C/T]ATTATGCTAACCTCT | 317 |
rs4609647 | snp | C/T | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98693832 | ttcttggcttacttt[C/T]tcagcttggtggaga | 317 |
rs4762502 | snp | A/G | 0.184521 | 0.241273 | intron-variant | APAF1 | GRCh38.p7 | 12:98667197 | aaactcctgggctcg[A/G]ttggtcctgagtagc | 317 |
rs4762503 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98708259 | cCAAACTTCTTACCT[C/G/T]GTGGATTGGTATCAA | 317 |
rs4762504 | snp | A/G | 0.499872 | 0.0079862 | intron-variant | APAF1 | GRCh38.p7 | 12:98718302 | cagtggtgcaatctc[A/G]gctcactgaaacctc | 317 |
rs4762505 | snp | A/C | 0.185155 | 0.241444 | intron-variant | APAF1 | GRCh38.p7 | 12:98720514 | GAAGTTATTGCCAAA[A/C]TTTGAAGAATCAGCT | 317 |
rs5800361 | in-del | -/A | 0.356811 | 0.226034 | intron-variant | APAF1 | GRCh38.p7 | 12:98724895 | AGACAATATTGAAAG[-/A]AAAAAAAAATAGCAT | 317 |
rs6538879 | snp | A/G | 0.349452 | 0.229367 | intron-variant | APAF1 | GRCh38.p7 | 12:98694316 | ACAGCAAAAGAAACT[A/G]TCAACAGAGTAAACT | 317 |
rs6538880 | snp | A/G | 0.184521 | 0.241273 | intron-variant | APAF1 | GRCh38.p7 | 12:98727770 | ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA | 317 |
rs6538881 | snp | A/T | 0.350546 | 0.22889 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734223 | TCCCTTGTCTCTCTC[A/T]TCCTCTTTTCCTTCC | 317 |
rs6538882 | snp | C/T | 0.350546 | 0.22889 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734224 | CCCTTGTCTCTCTCA[C/T]CCTCTTTTCCTTCCT | 317 |
rs7132133 | snp | A/C/T | | | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644870 | CATCCTCGTTGCTTC[A/C/T]CTGAGTCTTTCAGCT | 317 |
rs7138008 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98654835 | ttttttttttttttt[A/T]aatttatttttttat | 317 |
rs7297940 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650501 | caaaaaaaaGTTTTT[G/T]GTTTTTTTTTTTTTG | 317 |
rs7298561 | snp | A/G | 0.349233 | 0.229462 | intron-variant | APAF1 | GRCh38.p7 | 12:98677065 | TTTGAAGGTATCCTT[A/G]TATAATGATTTATCT | 317 |
rs7299536 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | APAF1 | GRCh38.p7 | 12:98707632 | CTAATACAGCATTAT[A/G]TATGAATTATAGCTA | 317 |
rs7299740 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | APAF1 | GRCh38.p7 | 12:98707969 | tttgtttttttgaga[C/T]ggagtctcgctctgt | 317 |
rs7300187 | snp | G/T | 0 | 0 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735763 | GTGAGCAAAACAAAA[G/T]TCTTGCTCTACTGCA | 317 |
rs7302131 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | APAF1 | GRCh38.p7 | 12:98704283 | AGATAGATTAGTTTT[C/T]CCAGGCTTTCTTAGT | 317 |
rs7302510 | snp | A/T | | | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644393 | TTCCTTCCTTTGGGG[A/T]CAAGACAGAGGCACA | 317 |
rs7303112 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | APAF1 | GRCh38.p7 | 12:98678114 | TAGGATACTTTTAGT[C/T]TTTGCAAGATTATGA | 317 |
rs7303489 | snp | C/G | 0.48491 | 0.0855403 | intron-variant | APAF1 | GRCh38.p7 | 12:98648127 | tgcattcattttcta[C/G]tttccccaattagtg | 317 |
rs7303874 | snp | A/G | 0.26326 | 0.249648 | intron-variant | APAF1 | GRCh38.p7 | 12:98678455 | gttcctgctgtagcc[A/G]cccaagccacagctg | 317 |
rs7304836 | snp | A/T | 0.428182 | 0.17536 | intron-variant | APAF1 | GRCh38.p7 | 12:98727970 | AATAAATAAATAAAT[A/T]AATTAATTAATTAAT | 317 |
rs7307338 | snp | A/G | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98679096 | CTGGAGTGGGAACTT[A/G]TAGTGCCTTTTCCAG | 317 |
rs7311388 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | APAF1 | GRCh38.p7 | 12:98715761 | ATCCTCTGTTGGAAG[G/T]TTGTTTATTTTGAAA | 317 |
rs7311426 | snp | G/T | 0.186737 | 0.241863 | intron-variant | APAF1 | GRCh38.p7 | 12:98683965 | TTTTTTCCTCTTAAG[G/T]GGATAAAGATAGCTA | 317 |
rs7311674 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | APAF1 | GRCh38.p7 | 12:98710163 | ataggtgtgagccac[C/T]gtgcccggccTAAGG | 317 |
rs7312213 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650494 | tccatctcaaaaaaa[A/G]GTTTTTTGTTTTTTT | 317 |
rs7312463 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | APAF1 | GRCh38.p7 | 12:98650641 | TGTACACATGGCCTC[A/G]GTTTAATTTCATAGC | 317 |
rs7312536 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650495 | ccatctcaaaaaaaa[G/T]TTTTTTGTTTTTTTT | 317 |
rs7312538 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98650502 | aaaaaaaaGTTTTTT[G/T]TTTTTTTTTTTTTGA | 317 |
rs7313090 | snp | A/G | 0.18325 | 0.240924 | intron-variant | APAF1 | GRCh38.p7 | 12:98680994 | TCAGTGGAAAACCAG[A/G]TGGATGAACAAACTA | 317 |
rs7313725 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98726139 | CTTAAGATATACATA[C/G]AAACCATGCCAATTT | 317 |
rs7314884 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | APAF1 | GRCh38.p7 | 12:98716277 | tgTTGCTTTTTTCCG[A/C]CTTCCACCTGTCCTG | 317 |
rs7314932 | snp | A/G | 0.269267 | 0.249256 | intron-variant | APAF1 | GRCh38.p7 | 12:98716423 | GGGTACTGTGAATGC[A/G]TTTTTTGCCTTAACG | 317 |
rs7315397 | snp | A/G | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98656588 | CCAAATTCTGATCTA[A/G]GTCTTCTTCTGTCAT | 317 |
rs7315547 | snp | C/T | 0.350982 | 0.228698 | intron-variant | APAF1 | GRCh38.p7 | 12:98707663 | AAATTCATTCAGTGC[C/T]TACTATATTCAAGAC | 317 |
rs7316588 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | APAF1 | GRCh38.p7 | 12:98711446 | GAGAGAAGATGTTCA[C/G]CTCTTCGTAGTTCAA | 317 |
rs7962978 | snp | A/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98689385 | TCGATTTCACTTGCC[A/G]TATTTTTTAATGCCC | 317 |
rs7963431 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689434 | GCCTTTTGTGTGAGG[A/G]Tgagagagagagaga | 317 |
rs7963562 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689581 | cctcctgcctcaacc[G/T]cctgagtagctggga | 317 |
rs7963569 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689605 | gctgggacttcaggc[A/G]tgtgtgacaatgcct | 317 |
rs7963633 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | APAF1 | GRCh38.p7 | 12:98689928 | TCTGTTTCTTTGATT[A/G]GGTTGAATATAGGTT | 317 |
rs7965985 | snp | C/T | 0.484771 | 0.0859212 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665359 | ATAATCAGGAACTTA[C/T]TGAATGAAATCTTTC | 317 |
rs7966685 | snp | A/C/G | 0.030278 | 0.119257 | intron-variant | APAF1 | GRCh38.p7 | 12:98690177 | CTGATACTCTGGTTG[A/C/G]ATCTTTGATCTTGCT | 317 |
rs7977880 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689174 | GGAAACGCAGACTCA[C/T]TGGGATGACTTCTAA | 317 |
rs7978375 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689575 | agtgatcctcctgcc[C/T]caaccgcctgagtag | 317 |
rs7980303 | snp | C/T | 0.181022 | 0.240296 | intron-variant | APAF1 | GRCh38.p7 | 12:98702113 | ctctttcgcccaggc[C/T]ggagtgcagtggcgc | 317 |
rs9668836 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693359 | tcagcctcccaaagt[A/G]ctgggcttacaagca | 317 |
rs9668841 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693477 | attgagccgtatcgt[A/G]tgaatttttttcctc | 317 |
rs9668846 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693701 | aatggtaatactatt[A/C]ccagagtccagctgc | 317 |
rs9669341 | snp | G/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98693483 | ccgtatcgtgtgaat[G/T]tttttcctctctcat | 317 |
rs9669349 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693556 | tttgtttagttttta[A/T]atgtgcttatcttca | 317 |
rs9669753 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693780 | cttttaaattggaac[A/C]cttgtttttcagttt | 317 |
rs10082736 | snp | A/G | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98652416 | CTTCTATAAAGTTGT[A/G]TCTTTTACTTTGCAT | 317 |
rs10161526 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98716187 | attaccttcatgcct[A/C]tatatggcatgctta | 317 |
rs10431447 | snp | C/G | 0.184838 | 0.241358 | intron-variant | APAF1 | GRCh38.p7 | 12:98728546 | CCAACATGGCAAAAC[C/G]CCATCTCTGCTAAAA | 317 |
rs10437887 | snp | A/G | 0.167158 | 0.235875 | intron-variant | APAF1 | GRCh38.p7 | 12:98721101 | CCAAACTCAACTTTT[A/G]CATTTGACTAATGGT | 317 |
rs10437888 | snp | A/G | 0.185472 | 0.241529 | intron-variant | APAF1 | GRCh38.p7 | 12:98721441 | ATCCTCCAGTCCAGT[A/G]AAGCCCAGAAAGCGG | 317 |
rs10541967 | snp | C/G | 0.444444 | 0.157135 | intron-variant | APAF1 | GRCh38.p7 | 12:98689474 | AGAGAGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 317 |
rs10562439 | in-del | -/GA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689436 | CTTTTGTGTGAGGGT[-/GA]GAGAGAGAGAGAGAG | 317 |
rs10578894 | in-del | -/AG | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98689463 | GAGAGAGAGAGAGAG[-/AG]TGTGTGTGTCTGTGT | 317 |
rs10668292 | in-del | -/TA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707692 | ATATATATATATATA[-/TA]CATATAAATTTACTA | 317 |
rs10718979 | in-del | -/A | 0.375 | 0.216506 | intron-variant | APAF1 | GRCh38.p7 | 12:98727547 | GCGACATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 317 |
rs10745833 | snp | A/T | 0.499759 | 0.0109798 | intron-variant | APAF1 | GRCh38.p7 | 12:98662347 | GCCATCTATTTGTTT[A/T]AAAAAAAATTTAATT | 317 |
rs10745834 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | APAF1 | GRCh38.p7 | 12:98666572 | ACGTGTTCTTTTTGT[A/G]GTCCAGGCCAATTTA | 317 |
rs10745836 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | APAF1 | GRCh38.p7 | 12:98701397 | ATATGGTAATTCTTT[A/G]TTTATTTAGTTTTCT | 317 |
rs10777940 | snp | C/T | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98652749 | GTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 317 |
rs10777943 | snp | C/T | 0.499265 | 0.0191552 | intron-variant | APAF1 | GRCh38.p7 | 12:98701004 | CTTTGTTTTTTTTTT[C/T]CTTACAAACCAGTGT | 317 |
rs10860356 | snp | A/T | 0.484701 | 0.0861117 | intron-variant | APAF1 | GRCh38.p7 | 12:98649905 | GAAAGAATAAAAGTT[A/T]GCTAGGCAGTGAAGG | 317 |
rs10860358 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | APAF1 | GRCh38.p7 | 12:98687090 | ATAATGTAGGCTGGG[C/T]GCGGTGGCTCACGCC | 317 |
rs10860359 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | APAF1 | GRCh38.p7 | 12:98716669 | ATTCATTGTTTTGGA[C/T]ATTCAGTCTTCCTTT | 317 |
rs10860361 | snp | A/G | 0.499154 | 0.0205497 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735719 | TGTACCATGTGCCTG[A/G]CATTGTGGTAGGTAT | 317 |
rs11109556 | snp | A/G | 0.0460142 | 0.144533 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645389 | CAGTCGGCGACCCGC[A/G]AAGACTTGAGGTGCC | 317 |
rs11109557 | snp | A/G | 0.293807 | 0.246132 | intron-variant | APAF1 | GRCh38.p7 | 12:98650379 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 317 |
rs11109558 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | APAF1 | GRCh38.p7 | 12:98652584 | AGGAGTTTCTTATAT[A/G]TTCTAGACATTAAAC | 317 |
rs11109559 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653691 | aaaaaaaaaaaAAAa[A/T]atatatatatatata | 317 |
rs11109560 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653693 | aaaaaaaaaAAAAAa[A/T]atatatatatatata | 317 |
rs11109561 | snp | A/G | 0.186421 | 0.24178 | intron-variant | APAF1 | GRCh38.p7 | 12:98662308 | AGAGTATAGCAAAGA[A/G]GAAGAATCATTTTCC | 317 |
rs11109562 | snp | A/T | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665276 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 317 |
rs11109563 | snp | A/T | 0 | 0 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665278 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 317 |
rs11109564 | snp | A/G | 0.264358 | 0.249587 | intron-variant | APAF1 | GRCh38.p7 | 12:98666122 | TTTTTTGTGTGTGTG[A/G]TAATACCTGTCTACA | 317 |
rs11109565 | snp | A/G | 0.254385 | 0.249962 | intron-variant | APAF1 | GRCh38.p7 | 12:98667035 | TAATGTTGATAATTT[A/G]TTTAAAGTGGTATCT | 317 |
rs11109566 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668134 | TGTTGTTGTCGTCGT[C/T]GTTTGGTATTTTGCT | 317 |
rs11109568 | snp | C/G | 0.270892 | 0.249126 | intron-variant | APAF1 | GRCh38.p7 | 12:98670554 | AACTTCTTTGGTCTT[C/G]AGTTTAATTTATATT | 317 |
rs11109569 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98672763 | ATTTTATTTTATTTT[A/T]TTTTTTTTGAGACGG | 317 |
rs11109570 | snp | C/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98678285 | TGTGCTCTGACACTT[C/T]TTTTTGATGGCAGCG | 317 |
rs11109571 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98685429 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTTC | 317 |
rs11109572 | snp | A/T | 0.299916 | 0.244966 | intron-variant | APAF1 | GRCh38.p7 | 12:98689495 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACACAG | 317 |
rs11109573 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | APAF1 | GRCh38.p7 | 12:98693070 | ATTTTTTGACTAAAA[A/C]AAAAAAACAACACAT | 317 |
rs11109574 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702668 | cgtctctactaaaaa[A/T]aaaaaaattagctgg | 317 |
rs11109575 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710200 | TTTTTTTTTTTTTTG[G/T]ATTTTTAGTAGAGAT | 317 |
rs11109576 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | APAF1 | GRCh38.p7 | 12:98712589 | TGACACGATCACAGC[C/T]GACTGCAGCCTTGAC | 317 |
rs11109577 | snp | C/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98714842 | GAAAGCCTTTTTTTT[C/T]CTTTTTTTTTTTTTG | 317 |
rs11109578 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714843 | AAAGCCttttttttt[C/T]tttttttttttttGA | 317 |
rs11109579 | snp | G/T | 0.482534 | 0.0918038 | intron-variant | APAF1 | GRCh38.p7 | 12:98715220 | ATATGTTTGCATGTA[G/T]GCATACATGGTGTGC | 317 |
rs11109580 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720976 | tgtctcaaaaaaaaa[A/G]aaaaaaaaaaTTTCC | 317 |
rs11109581 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98720977 | gtctcaaaaaaaaag[A/G]aaaaaaaaaTTTCCT | 317 |
rs11109582 | snp | A/G | 0.453697 | 0.14494 | intron-variant | APAF1 | GRCh38.p7 | 12:98723141 | CTCTCCACCCCTCCA[A/G]TGAGATAGGATCGGG | 317 |
rs11109583 | snp | C/T | 0.0276762 | 0.114333 | intron-variant | APAF1 | GRCh38.p7 | 12:98725577 | GAGCACTGCTCTTCT[C/T]GTAGCTTGGGCTAGC | 317 |
rs11109584 | snp | A/G | 0.142609 | 0.225759 | intron-variant | APAF1 | GRCh38.p7 | 12:98727901 | agccgagatcacacc[A/G]ttgcactgcagccta | 317 |
rs11296996 | in-del | -/A | 0.476918 | 0.104919 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733918 | CTTCTTACTTGAATG[-/A]AACCTGATCTTTCCT | 317 |
rs11334064 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98661767 | GAGTATTTTTTTTTT[-/T]GTAATGCACAGCCAT | 317 |
rs11335734 | in-del | -/A | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98706710 | TGAGGTAAGCAGAAT[-/A]GGAAACTAGTACTAT | 317 |
rs11613414 | snp | C/G/T | 1.6651e-05 | 0.00288535 | intron-variant | APAF1 | GRCh38.p7 | 12:98667689 | TCTGACTTCCCTTTT[C/G/T]CCATATGTATTACAA | 317 |
rs11613534 | snp | A/C | 0.0136048 | 0.0813469 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671665 | AAGTTTATCAGCAAG[A/C]TAAGCTGCAGGCCAA | 317 |
rs11614667 | snp | G/T | 0.00934559 | 0.067716 | intron-variant | APAF1 | GRCh38.p7 | 12:98673622 | ATCTTTATGGCATTA[G/T]GCCCTCTTTCCAAAT | 317 |
rs11829360 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | APAF1 | GRCh38.p7 | 12:98717119 | gtgatccgcccgcct[C/T]ggcctcccaaagtgc | 317 |
rs11830511 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | APAF1 | GRCh38.p7 | 12:98694250 | cctcaaaagcaattg[C/T]tacaaaaacaaactt | 317 |
rs11830551 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98655299 | cgcctttctattcca[C/T]aaagccgccattgtc | 317 |
rs11830651 | snp | G/T | 0.0637235 | 0.166737 | intron-variant | APAF1 | GRCh38.p7 | 12:98694839 | gtgaacTTTTAAATT[G/T]TGGTTTTCCTATGGG | 317 |
rs11831003 | snp | A/G | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98707679 | TACTATATTCAAGAC[A/G]TTATGCAAAGTACTA | 317 |
rs11831799 | snp | A/C | 0.444444 | 0.157135 | intron-variant | APAF1 | GRCh38.p7 | 12:98673461 | AAAAAAAAAAACAAA[A/C]AAAAAACCTTGGGTC | 317 |
rs11832663 | snp | C/T | 0.0169455 | 0.0904743 | intron-variant | APAF1 | GRCh38.p7 | 12:98683140 | TTTCTCTTTTCTCTT[C/T]AGATTTGGAATTCTA | 317 |
rs11833466 | snp | A/G | 0.221919 | 0.248418 | intron-variant | APAF1 | GRCh38.p7 | 12:98693810 | ttttttttttttttc[A/G]tcttctttcttggct | 317 |
rs11833684 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | APAF1 | GRCh38.p7 | 12:98681969 | GAAGGTTCATTAGGT[A/G]ATTTATTTCTTTTGT | 317 |
rs11835097 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98662299 | ATATTGAGAAGAGTA[C/T]AGCAAAGAGGAAGAA | 317 |
rs11836211 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | APAF1 | GRCh38.p7 | 12:98708223 | gtgctgggattacag[A/G]tgtgagcccctgcgc | 317 |
rs11836469 | snp | A/C | 0.0332131 | 0.124513 | intron-variant | APAF1 | GRCh38.p7 | 12:98673457 | CAAAAAAAAAAAAAA[A/C]AAAAAAAAAACCTTG | 317 |
rs11836812 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98675630 | attgtactaggtatt[C/T]tgagtaatctataga | 317 |
rs11836984 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | APAF1 | GRCh38.p7 | 12:98709474 | GCCCTAAGGAGCACT[A/G]GAATTCAAGAGCAGG | 317 |
rs11837006 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | APAF1 | GRCh38.p7 | 12:98709542 | TGCATTGACAGAGAT[A/G]TCCTGGAAGTGGTGA | 317 |
rs11837552 | snp | C/T | 0.249603 | 0.25 | intron-variant | APAF1 | GRCh38.p7 | 12:98680039 | GCCAGAAAATCAACA[C/T]CCCAAAGATCCTGTA | 317 |
rs12049976 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647845 | taaaatctatattca[A/G]aatgatggacattta | 317 |
rs12049983 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98648040 | tgaagtaaatcctta[A/G]aaatgggatttctgg | 317 |
rs12099502 | snp | A/C | 0.030278 | 0.119257 | intron-variant | APAF1 | GRCh38.p7 | 12:98658876 | GTGCTGTGCAGTGAT[A/C]ACTGACAACACAGGA | 317 |
rs12099604 | snp | A/G | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98673416 | ACTCCAGCCTGGGCA[A/G]CAAAGTGAAGCTCTG | 317 |
rs12099698 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98668705 | ccccagtggaaagaa[C/T]ggagtccatgaactg | 317 |
rs12099797 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | APAF1 | GRCh38.p7 | 12:98676793 | ctgggattacaggca[C/T]gtgccaccacaccca | 317 |
rs12299716 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98713685 | GTGGTTTTTCAAAAA[C/T]CTTGGTTCCTTCTCT | 317 |
rs12304057 | snp | A/G | 0.0463947 | 0.145069 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643495 | CTCCTCCCGCCAGAA[A/G]AAAAAAGGCTGGGAA | 317 |
rs12304328 | snp | C/T | 0.140908 | 0.224942 | intron-variant | APAF1 | GRCh38.p7 | 12:98696795 | gccactgcaccctgc[C/T]GGGAGTAATCAGTCT | 317 |
rs12307986 | snp | A/G | 0.0283406 | 0.115616 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733323 | tttttagtagagacg[A/G]ggtttcaccatgttg | 317 |
rs12313788 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | APAF1 | GRCh38.p7 | 12:98722566 | TCTCAGATACGTTTG[C/T]ATGCATATTTTGTGC | 317 |
rs12316526 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | APAF1 | GRCh38.p7 | 12:98720982 | aaaaaaaaagaaaaa[A/G]aaaaTTTCCTTAACA | 317 |
rs12368223 | snp | A/C | 0.126219 | 0.217206 | intron-variant | APAF1 | GRCh38.p7 | 12:98696352 | ccagactgttttcaa[A/C]aacccgcactcttga | 317 |
rs12368428 | snp | C/G | 0.269538 | 0.249235 | intron-variant | APAF1 | GRCh38.p7 | 12:98721890 | GCTGTTTAACATTGG[C/G]CAATAAAAAGCTAGA | 317 |
rs12368451 | snp | A/G | 0.499587 | 0.0143711 | intron-variant | APAF1 | GRCh38.p7 | 12:98721883 | TATTTCTGCTGTTTA[A/G]CATTGGCCAATAAAA | 317 |
rs12369297 | snp | A/T | 0.484771 | 0.0859212 | intron-variant | APAF1 | GRCh38.p7 | 12:98656293 | ACTTTATTCTCTGCA[A/T]TTATAAATATATACA | 317 |
rs12370618 | snp | A/T | 0.264358 | 0.249587 | intron-variant | APAF1 | GRCh38.p7 | 12:98694445 | TGCTTGTGTTTCTGG[A/T]TTAAaattttttttc | 317 |
rs12426636 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | APAF1 | GRCh38.p7 | 12:98700328 | TCACTTACATTCTCA[G/T]CTAATAGTGATTTCA | 317 |
rs12578662 | snp | C/T | 0.264632 | 0.249571 | intron-variant | APAF1 | GRCh38.p7 | 12:98679244 | agcaacccactctag[C/T]gccccctctttgctg | 317 |
rs12580228 | snp | C/T | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98668128 | TACCACTGTTGTTGT[C/T]GTCGTTGTTTGGTAT | 317 |
rs12581119 | snp | A/G | 0.437118 | 0.165792 | intron-variant | APAF1 | GRCh38.p7 | 12:98718545 | CCTTCTTTTTTATGT[A/G]AAATCAAGTTTCCTA | 317 |
rs12581708 | snp | A/G | 0.148326 | 0.228391 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735844 | AATTTGGTGGTATGT[A/G]CAAGCGGAGGGGAAG | 317 |
rs12581724 | snp | C/T | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98663074 | TGTGACCTCTGCTGT[C/T]AGAGTTAAAAATAGA | 317 |
rs12581734 | snp | C/T | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98663143 | TTTATAAAAATAGTG[C/T]TCTAATTTGGTAAGT | 317 |
rs12582226 | snp | A/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98675115 | CTTATTTTTAAATTG[A/T]GTTTGACCAGTCCAT | 317 |
rs12582317 | snp | C/G | 0.249603 | 0.25 | intron-variant | APAF1 | GRCh38.p7 | 12:98679081 | tgtggactgaatgga[C/G]tggagtgggaactta | 317 |
rs12813112 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | APAF1 | GRCh38.p7 | 12:98678873 | tttgggtgctgatga[A/G]cataggagggaagcc | 317 |
rs12816094 | snp | A/C | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98691483 | GGCTTCTTAAGTCAT[A/C]TATACTTGCCTCTGT | 317 |
rs12816253 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691536 | TTAACCATTTTTTAG[C/T]CTGGTTTCATCTTCC | 317 |
rs12816300 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691614 | AATTTTTTTTGTAGT[A/C]TAAGGCCCTCTGGAT | 317 |
rs12816581 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691535 | CTTAACCATTTTTTA[G/T]CCTGGTTTCATCTTC | 317 |
rs12816623 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691612 | TCAATTTTTTTTGTA[C/G]TCTAAGGCCCTCTGG | 317 |
rs12817338 | snp | G/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98691423 | TCCTTGATTGTATTG[G/T]TCTTTAAAATTGTCA | 317 |
rs12817484 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691444 | AAAATTGTCATTCTG[G/T]TTTTCTCTTTCCCTT | 317 |
rs12817709 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98691572 | TTCCCTTGAAGAATG[A/T]AAAAATCCAGTTTTA | 317 |
rs12819455 | snp | C/T | 0.00566568 | 0.052922 | intron-variant | APAF1 | GRCh38.p7 | 12:98688397 | CCTGATAGCAACCAT[C/T]TAAGATGCATTCTGC | 317 |
rs12826701 | snp | C/G | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98689468 | agagagagagagtgt[C/G]tgtgtctgtgtgtgt | 317 |
rs12829605 | snp | G/T | 0.268995 | 0.249277 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733653 | tgtctaggctggtct[G/T]gaactcttggcctca | 317 |
rs12831555 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647991 | CATTAATTCTccttg[G/T]ggatatttttacata | 317 |
rs17028590 | snp | A/G | 0.202035 | 0.245356 | intron-variant | APAF1 | GRCh38.p7 | 12:98677903 | ATTAGGAAAATACCT[A/G]TTTTATCAAAGTCTT | 317 |
rs17028602 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | APAF1 | GRCh38.p7 | 12:98686390 | TTAAAAAATATGGGG[G/T]TAATTTATATTACAT | 317 |
rs17028605 | snp | C/T | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98686542 | TTTGAGTCCCTTAGT[C/T]GATTTACATGCTGAT | 317 |
rs17028634 | snp | C/G/T | 0.0528381 | 0.153711 | intron-variant | APAF1 | GRCh38.p7 | 12:98698578 | ATACTTCTTTTTACT[C/G/T]GAGAGATTTGAAAAT | 317 |
rs17028651 | snp | A/C | 0.0490535 | 0.14873 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731419 | TTAGTGACTGAAAAC[A/C]AATGAATCTCAGGTT | 317 |
rs17028653 | snp | C/T | 0.0535932 | 0.154675 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731855 | CTACAGCCCTTGCTA[C/T]GTTTGAGATGTTCAG | 317 |
rs17041383 | snp | C/T | 0.366885 | 0.220993 | intron-variant | APAF1 | GRCh38.p7 | 12:98702429 | AGGTCTATGTCTTGA[C/T]CTTAAATCAGTATAT | 317 |
rs17227584 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | APAF1 | GRCh38.p7 | 12:98684891 | AAGGACAAGGTTTAC[C/T]TTAAGATGTGCTATA | 317 |
rs17227606 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732853 | AATTCTGTCTTGATG[C/T]ATTCAAAATGGTTGA | 317 |
rs17815365 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98699235 | TCTTTTTAAGAACGT[A/G]ATAATGAAACTGGAG | 317 |
rs28489427 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647909 | TTCTTTTTTCTTTTT[A/C/T]TTTTTTACTCTAGCC | 317 |
rs28544215 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98673449 | TCAAAAAACAAAAAA[A/C]AAAAAAACAAAAAAA | 317 |
rs28548709 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98647902 | CCATTAATTCTTTTT[C/T]CTTTTTATTTTTTAC | 317 |
rs28626683 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653458 | GGTCAGGAGTTTGAG[A/C]CCAGCCTGGCCAACA | 317 |
rs28661533 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | APAF1 | GRCh38.p7 | 12:98688668 | TTTTTTTTAGAGATA[A/G]GATCTTACTATGTTG | 317 |
rs34019025 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98654835 | TTTTTTTTTTTTTTT[-/T]AATTTATTTTTTTAT | 317 |
rs34021924 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707293 | ATTTTCCCAAACACT[-/C]CCGTAGTTCCCTGCT | 317 |
rs34038166 | in-del | -/T | | | intron-variant, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98729783 | ACATGAGACCCACAC[-/T]AGCTGCAATTTTACC | 317 |
rs34108074 | in-del | -/T | 0.0197608 | 0.0974162 | intron-variant | APAF1 | GRCh38.p7 | 12:98726180 | ACAATCTATTTTTTT[-/T]AGATATATAATTTTG | 317 |
rs34144325 | snp | C/T | 0.293807 | 0.246132 | intron-variant | APAF1 | GRCh38.p7 | 12:98651142 | TTAATTCATATTCCT[C/T]GTACTTTTGTGGGAT | 317 |
rs34273507 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | APAF1 | GRCh38.p7 | 12:98656865 | TACTCCCTTCTCCAG[C/T]TGAATGCTTTGAGGT | 317 |
rs34313440 | in-del | -/A | 0.476833 | 0.105105 | intron-variant | APAF1 | GRCh38.p7 | 12:98728558 | AACCCCATCTCTGCT[-/A]AAAAATACAAAAATT | 317 |
rs34325673 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715088 | TTTTTTTTTTTTTTT[-/T]GGAGGGCAAGCCCAG | 317 |
rs34461602 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685625 | GGTGTGAGCCACCAC[-/G]GCCCAGCTTATAAAC | 317 |
rs34463741 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700087 | GGAAAATATGAAAAA[-/G]AGTAAATAAGAAAAT | 317 |
rs34499194 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703055 | TTTTGAATAAACAAG[-/C]CATTAGGGAGAACTA | 317 |
rs34536171 | in-del | -/A/AA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98659752 | GTGAAACTCCATCAG[-/A/AA]AAAAAAAAAAAAAAA | 317 |
rs34546993 | in-del | -/TC | 0.262435 | 0.249691 | intron-variant | APAF1 | GRCh38.p7 | 12:98674439 | CTTGTGAAGTGGAGG[-/TC]TCTCTCTCTCTCTCT | 317 |
rs34602173 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688639 | TCACACCTGGCGAAA[-/T]TTTTTTTTTTTTTTT | 317 |
rs34602753 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666269 | TAAGTCTCTTTTATT[-/C]CTGTGATCGGAATGG | 317 |
rs34745438 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98685683 | TCTATCACCCAGGCT[-/G]GGAGTGCAGTGGAGC | 317 |
rs34768177 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98658945 | AAGCCACAGATTTAC[-/T]TTCAAACTTCAGTTT | 317 |
rs34774971 | in-del | -/T | 0.300169 | 0.244914 | intron-variant | APAF1 | GRCh38.p7 | 12:98676650 | GTTTTTTTTTTTTTT[-/T]GAAATGGAGTCTTGC | 317 |
rs34777464 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98714024 | TAAAGTACATCATGG[-/G]ATATGTATTTCTTAA | 317 |
rs34779436 | in-del | -/C/TC/TTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688641 | CACCTGGCGAAATTT[-/C/TC/TTT]TTTTTTTTTTTTTTT | 317 |
rs34850935 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653689 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 317 |
rs34873465 | snp | C/T | 0.206073 | 0.246111 | intron-variant | APAF1 | GRCh38.p7 | 12:98667497 | CTGGCTTCTGAAACG[C/T]TTCATTGGGTTGCAG | 317 |
rs34976764 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712625 | AGCTCAAGTGATTTT[-/C]CCCACTTAAGCCTCC | 317 |
rs34980617 | in-del | -/A | 0.259951 | 0.249802 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730819 | AAATTGAGTGCCAGT[-/A]AAGATAAAGTAGGTA | 317 |
rs35049411 | snp | A/G | 0.0195694 | 0.0969626 | intron-variant | APAF1 | GRCh38.p7 | 12:98690001 | CTTTCTTTGTAACTC[A/G]TAGTACAGAATTGTA | 317 |
rs35051816 | snp | C/T | 0.00981408 | 0.0693594 | intron-variant | APAF1 | GRCh38.p7 | 12:98698758 | CTGAGACACTGCTCA[C/T]GGCCCAGAGGARTGA | 317 |
rs35067498 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98700461 | ATTTAGTGCTACAAT[-/C]CCTTGGATGTTGGTT | 317 |
rs35072360 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707094 | GCAGCTTCTAAGATA[-/T]TTTTTTTTTCATGTA | 317 |
rs35094611 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688639 | TCACACCTGGCGAAA[-/T]TTTTTTTTTTTTTTT | 317 |
rs35097930 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649956 | GGTGGGAAAGGTAGT[-/G]GGGTGGTTACTGGGG | 317 |
rs35152045 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708333 | GGGTTAAGCAACCTG[-/C]CCTGAAGTTACAACT | 317 |
rs35186423 | in-del | -/C | | | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98729942 | GGGAAATTATAGTTA[-/C]ACAATTTATTGTATA | 317 |
rs35203836 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98726408 | GTAGATGAGGAAGAT[-/G]GGGGTTTTCCCCCTT | 317 |
rs35326207 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98649090 | GCCCTTGTTTATTTT[-/C]CCAGTTCTATGTGTT | 317 |
rs35404649 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684702 | GGTTCACTTTTACTC[-/A]AAAAAACTTGGCCCT | 317 |
rs35491776 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708329 | CACTGGGTTAAGCAA[-/C]CCTGCCTGAAGTTAC | 317 |
rs35614669 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98722128 | TCCCTTTTCACGTTT[-/C]CCCTGCTCCTATACT | 317 |
rs35681517 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | APAF1 | GRCh38.p7 | 12:98724281 | GTGCATCTTAGAGTT[A/G]TCTTCTCCTCTTTGT | 317 |
rs35688852 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98720448 | TTTTAATTATCTTTG[C/T]ATCCCCAAAGCCTGG | 317 |
rs35715320 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | APAF1 | GRCh38.p7 | 12:98673764 | GTTACTAGATGTGAG[A/G]TCTTTCCCCTAAGGA | 317 |
rs35746294 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734295 | AAATAGCTTTTGACA[-/G]GGGGAAAAAACTCAA | 317 |
rs35750533 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98723341 | TAAATTTGTTTTTTG[-/A]AAAAGTATTCTCATA | 317 |
rs35760675 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681254 | TTGGTAGAGACAGAG[-/T]TTTTGCCATGTTGGT | 317 |
rs35810153 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709427 | GTATTCAGGAGCTCG[A/G]AGTGGTGGTAACAGA | 317 |
rs35957629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98690201 | TCTTGCTTTGCTGAC[A/G]GAAGATAACTGTTTT | 317 |
rs35979016 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98724764 | AAACTATAAACTTTT[-/C]CAAGGATAGTGACTG | 317 |
rs36077634 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98709417 | CAGAGGAATGGTATT[A/C]AGGAGCTCGGAGTGG | 317 |
rs36091713 | in-del | -/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98652020 | GGTTTTGTCATGTTA[-/C]CCGAGGTTGGTCTCG | 317 |
rs41514747 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | APAF1 | GRCh38.p7 | 12:98704023 | ATTTTATGTTCAGAA[A/T]GTATACCTAGCTGGC | 317 |
rs56115813 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | APAF1 | GRCh38.p7 | 12:98716915 | CTGTCACCCAGGCTG[A/G]AGTGCAGTGGCGCGA | 317 |
rs56239900 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719589 | GATCTCTTGACCTTG[A/T]GATCCTCCCGCCTCA | 317 |
rs56241477 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98668918 | AATTATTAGCACATA[G/T]ATGGTATTTGATTGA | 317 |
rs56248141 | snp | C/T | 0.104859 | 0.203554 | intron-variant | APAF1 | GRCh38.p7 | 12:98653651 | GACAGAGTGAGATGC[C/T]GTCTCAAAAAAAAAA | 317 |
rs56394057 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | APAF1 | GRCh38.p7 | 12:98693075 | TTGACTAAAAAAAAA[A/C]AACAACACATATATA | 317 |
rs56947674 | snp | C/G | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98656376 | ATAACTGCAAACTTA[C/G]ACTGAAGGAGGCCTG | 317 |
rs57140718 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689461 | GAGAGAGAGAGAGAG[A/T]GAGTGTGTGTGTCTG | 317 |
rs57171247 | snp | C/T | 0.015186 | 0.0858043 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665674 | GAAATCTTCGTCTTA[C/T]GATTATGAGGCTCTA | 317 |
rs57391188 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689470 | AGAGAGAGAGTGTGT[C/G]TGTCTGTGTGTGTGT | 317 |
rs57738133 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694703 | CCAGTGTAATAGATA[A/T]TTTTCTATTTGTTGG | 317 |
rs58034998 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680993 | TTCAGTGGAAAACCA[A/G]GTGGATGAACAAACT | 317 |
rs58115001 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | APAF1 | GRCh38.p7 | 12:98704586 | AGTGAGGGCATGAGA[C/T]CCATAGGCTTCTCCT | 317 |
rs58431430 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | APAF1 | GRCh38.p7 | 12:98672417 | TGAGCTGCATGCCTC[C/G]GCCTCCCAAAGTGCT | 317 |
rs58671221 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98651685 | TTTTTTAAAGAGACA[G/T]AGTGTCACCCTGTTG | 317 |
rs58689985 | snp | C/G/T | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98652034 | TACCGAGGTTGGTCT[C/G/T]GAACTCCTGAGCTCA | 317 |
rs58713555 | in-del | -/AATATA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653691 | AAAAAAAAAAAAAAA[-/AATATA]TATATATATATATAT | 317 |
rs58734555 | in-del | -/A | | | intron-variant | APAF1 | GRCh38.p7 | 12:98687377 | AAAAAAAAAAAAAAA[-/A]GTTCTGTAATGTAGA | 317 |
rs58969166 | in-del | -/TATATAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653688 | AAAAAAAAAAAAAAA[-/TATATAT]AAAATATATATATAT | 317 |
rs59548547 | in-del | -/TTA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98727973 | AAATAAATAAATTAA[-/TTA]ATTAATTAATTAAAA | 317 |
rs60201657 | snp | A/G | 0.229723 | 0.249176 | intron-variant | APAF1 | GRCh38.p7 | 12:98656377 | TAACTGCAAACTTAC[A/G]CTGAAGGAGGCCTGA | 317 |
rs60275805 | in-del | -/C/CTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688642 | ACCTGGCGAAATTTT[-/C/CTT]TTTTTTTTTTTTTTT | 317 |
rs60298983 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719533 | TTTTTTTTTTTTTTT[-/T]AGTAGAGTTGGGGTT | 317 |
rs60521401 | snp | A/T | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98657596 | TTACATATAAGGTTC[A/T]GTTGGGCCTGCCTGA | 317 |
rs60570492 | snp | A/G | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98687357 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 317 |
rs60631192 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98696655 | AAACTTGGGAGTGAT[C/G]TTTTTGTTTGTTTGT | 317 |
rs60688334 | in-del | -/ATATATATATATATATATGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715281 | TATATATATATATAT[-/ATATATATATATATATATGA]GACATTCATTTGTTT | 317 |
rs60735761 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689463 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTCTGTG | 317 |
rs60760345 | snp | C/T | 0.0221141 | 0.102801 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98734943 | AAAGCCTTGAATGGC[C/T]CTTGTCTTAAAAAGA | 317 |
rs61061691 | in-del | -/AC/GA/GACA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689505 | TGTGTGAGAGAGAGA[-/AC/GA/GACA]CACAGGGTCTTACTT | 317 |
rs61222492 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664956 | CCACTTCTGTATTAT[G/T]GGACATTGTTTACGT | 317 |
rs61301412 | in-del | -/AAAAAAAAAAA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653682 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]TATATATATATATAT | 317 |
rs61430351 | in-del | -/ATATATATATAT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715270 | TATATATATATATAT[-/ATATATATATAT]GACATTCATTTGTTT | 317 |
rs61553790 | snp | A/G/T | 0.0592355 | 0.161582 | intron-variant | APAF1 | GRCh38.p7 | 12:98667112 | TGTATATATATATGT[A/G/T]TTTTTTTTTTTTTGA | 317 |
rs61742041 | snp | C/T | 0.000280077 | 0.0118305 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703439 | CAGCACCATCCAGTA[C/T]TGTGACTTCTCCCCA | 317 |
rs61757705 | snp | A/G | 0.000658794 | 0.0181373 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706570 | TGTTTTCTCCTGATG[A/G]ATCATCATTTTTGAC | 317 |
rs61758870 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671707 | ATAATGGAATGCTTT[A/T]CCTGGAATGGATGTA | 317 |
rs61758871 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677487 | ACACAGATGCTGTTT[A/C]CCATGCCTGCTTTTC | 317 |
rs61932038 | snp | G/T | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665395 | TCTAATTTTTTTTGG[G/T]ATAAATATCTAGAAG | 317 |
rs61932042 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98699741 | CGTGAGATAAGGATG[A/G]CCTTGTAAGGAAAGG | 317 |
rs61932043 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98713953 | TCAGGCTTTGTTTTC[C/T]CTTTATTATTGTGAA | 317 |
rs61932057 | snp | C/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731131 | TAGCTTTGTGACCTT[C/G]CACAAGATTGTTTAA | 317 |
rs66619012 | in-del | -/T | 0.225597 | 0.248806 | intron-variant | APAF1 | GRCh38.p7 | 12:98688471 | CCACTGTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 317 |
rs66849928 | in-del | -/T | 0.449726 | 0.150364 | intron-variant | APAF1 | GRCh38.p7 | 12:98647706 | GGGATCATGTTTCTG[-/T]TTTTTTTTTTTTTTT | 317 |
rs67353662 | in-del | -/T | 0.130694 | 0.219696 | intron-variant | APAF1 | GRCh38.p7 | 12:98714834 | GAAAGCCTTTTTTTT[-/T]CTTTTTTTTTTTTTG | 317 |
rs67372449 | snp | A/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98653683 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 317 |
rs67886092 | in-del | -/C | 0.190519 | 0.242821 | intron-variant | APAF1 | GRCh38.p7 | 12:98651666 | CTCTTTAAAAAAAAA[-/C]AAAAATAAATAAATA | 317 |
rs68164480 | in-del | -/A | 0.375 | 0.216506 | intron-variant | APAF1 | GRCh38.p7 | 12:98688660 | TAAGATCCTATCTCT[-/A]AAAAAAAAAAAAAAA | 317 |
rs68165158 | in-del | -/TGTG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689496 | GTGTGTGTGTGTGTG[-/TGTG]AGAGAGAGACACAGG | 317 |
rs71081873 | in-del | -/AG/CA | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98674462 | AGGGGGCTGCTTCTC[-/AG/CA]AGAGAGAGAGAGAGA | 317 |
rs71081876 | in-del | -/ATATAT | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98715276 | AAACAAATGAATGTC[-/ATATAT]ATATATATATATATA | 317 |
rs71305589 | in-del | -/A | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98667766 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 317 |
rs71305590 | in-del | -/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98659772 | CTTTCTTTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 317 |
rs71436926 | in-del | C/TG | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98661091 | TATTTTTAGTAGAGA[C/TG]AGGTTTCACCGTGTT | 317 |
rs71436927 | multinucleotide-polymorphism | AA/CC | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98691248 | GTACCTACTGTTCCT[AA/CC]CTTTCCTTCTTTTCC | 317 |
rs71436928 | in-del | -/A | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98720977 | AAAAAGAAAAAAAAA[-/A]TTTCCTTAACATTTC | 317 |
rs71436929 | in-del | -/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98722927 | TTTTCTATCTTCTGG[-/G]TATAATTAACTGTTC | 317 |
rs71436930 | in-del | -/A | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98722983 | TATTTAGGAGGAAAA[-/A]GTATTTTATTTTGCC | 317 |
rs71436931 | in-del | -/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98723052 | TGTGGACACCACAGT[-/T]CTTCTCTCTTATTCC | 317 |
rs71436932 | in-del | -/AAAT | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98727991 | ATTAATTAAAAAAAT[-/AAAT]AAAAAGGAAAAGAAA | 317 |
rs71443529 | in-del | -/AAA | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98710198 | CTCTACTAAAAATAC[-/AAA]AAAAAAAAAAAAAAA | 317 |
rs71462244 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98653680 | AAAAAAAAAAAAAAA[A/T]AATATATATATATAT | 317 |
rs71462245 | snp | C/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98678893 | GGAGGGAAGCCAAGG[C/G]GGTGCTGAGGGCAGT | 317 |
rs71462246 | snp | A/C | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98684493 | CTCCTCCTCCTCCTC[A/C]CTCCTCCTCCCCCCA | 317 |
rs71462247 | snp | A/C | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98684510 | TCCTCCTCCCCCCAC[A/C]CCCCCTCTCATTCTC | 317 |
rs71462248 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98722329 | GACTTTTTGGGTTTG[G/T]TGTTGTATTTCTCAT | 317 |
rs71462249 | snp | A/T | 0.153997 | 0.230832 | intron-variant | APAF1 | GRCh38.p7 | 12:98727974 | AATAAATAAATTAAT[A/T]AATTAATTAATTAAA | 317 |
rs71949084 | in-del | -/AT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98707702 | AGTACTATATATATA[-/AT]TATATATATACATAT | 317 |
rs72354759 | in-del | -/ATTT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98672165 | AGATTTTATTTATTT[-/ATTT]ATTTATTTATTTTTG | 317 |
rs73142304 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98669028 | GGTATGTTATTTCTT[A/G]GTTATGATACATAGT | 317 |
rs73142307 | snp | A/C | 0.0127354 | 0.0787751 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677505 | ATGCCTGCTTTTCTG[A/C]GGATGGTCAGAGAAT | 317 |
rs73142310 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | APAF1 | GRCh38.p7 | 12:98689075 | CTGCCTTGGCCTCCT[A/G]AAGTGCTGAGATTAT | 317 |
rs73142311 | snp | A/T | 0.106987 | 0.205054 | intron-variant | APAF1 | GRCh38.p7 | 12:98689120 | GCATCCGGCCCTACC[A/T]CTATTTTCAACATAA | 317 |
rs73142316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98726458 | AAAACTCCAGGAACA[A/G]GTATATAGTGCAGAA | 317 |
rs73142318 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734579 | GGGGAGAGGGTAAGG[A/G]AATAGATCACTCAGA | 317 |
rs73374754 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | APAF1 | GRCh38.p7 | 12:98650837 | TATTTCAGGATAAAT[G/T]TAGCTTAAGTTCCTT | 317 |
rs73374762 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | APAF1 | GRCh38.p7 | 12:98657862 | GCTTGATAGTGTGCT[A/G]TAGGATTAAATGAAT | 317 |
rs73374765 | snp | A/G | 0.270351 | 0.24917 | intron-variant | APAF1 | GRCh38.p7 | 12:98661421 | AGTCTCATTTGGTTT[A/G]TGCTTTTGTAATTTT | 317 |
rs73374767 | snp | C/T | 0.268724 | 0.249298 | intron-variant | APAF1 | GRCh38.p7 | 12:98661894 | TTTTGGAGAGAACAA[C/T]TGGGAACTGGCATAG | 317 |
rs73374768 | snp | C/T | 0.268724 | 0.249298 | intron-variant | APAF1 | GRCh38.p7 | 12:98661901 | GAGAACAACTGGGAA[C/T]TGGCATAGAGGTTCT | 317 |
rs73374774 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | APAF1 | GRCh38.p7 | 12:98668079 | ATGAGCCACCGCGGC[C/T]GGCTGAAGATTTGAA | 317 |
rs73374795 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98681392 | TTTTTGTTAAGTATT[C/T]TCTTGTTCCTAAATT | 317 |
rs73378418 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | APAF1 | GRCh38.p7 | 12:98683801 | AGTGGGACAAATGAG[C/T]GAGGTCAACTCTACT | 317 |
rs73378420 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | APAF1 | GRCh38.p7 | 12:98684390 | CCCTTTCCCTCTCCT[C/G]TCTCTCTCTCCCTCT | 317 |
rs73378423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98684959 | CTTGTGATTCTTGAG[C/T]AGAGAGAAGCCAGTG | 317 |
rs73378440 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | APAF1 | GRCh38.p7 | 12:98699796 | AATATGTTTTGTATT[A/G]CTTTCCCCTATTAGG | 317 |
rs73378442 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98706938 | TCCAATTACTTGCCA[A/T]TTCTGAGAGAGTCTA | 317 |
rs73378448 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | APAF1 | GRCh38.p7 | 12:98709579 | TGTAGATAGTGGCAG[C/T]AAGAGAAAGCAGATG | 317 |
rs73378450 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | APAF1 | GRCh38.p7 | 12:98710503 | GACGAGAGTAATAGA[A/G]CACATGTGTGGAAGG | 317 |
rs73378457 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | APAF1 | GRCh38.p7 | 12:98721829 | AGGGGAATAAGAGAT[G/T]TCATTTATTTTAAGA | 317 |
rs73378459 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | APAF1 | GRCh38.p7 | 12:98723066 | GTCTTCTCTCTTATT[C/G]CTCTCTGTTTTACTG | 317 |
rs73378465 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | APAF1 | GRCh38.p7 | 12:98728319 | TTATAGTTTACAAAA[C/T]GCTTCACTCCCCTCA | 317 |
rs73378466 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98729910 | AAGGAGTAATTTCTA[G/T]TATTTGATAATACAG | 317 |
rs73378469 | snp | C/T | 0.0626037 | 0.165477 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731300 | ATTTGTTACAATTGA[C/T]GGATCCACATTGACA | 317 |
rs73378471 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731870 | CGTTTGAGATGTTCA[A/G]TATTTGTTTAGTAAA | 317 |
rs74337521 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98693753 | ATCATCCTAGGGATT[C/T]CTTTTGCTTTTCTTT | 317 |
rs74403939 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98659025 | TCTTGCACGTAAAAT[G/T]TCTACTCTAAATCAA | 317 |
rs74413253 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | APAF1 | GRCh38.p7 | 12:98675380 | AACATTTTAAAATCT[A/T]ATCCTCTTAACTTTG | 317 |
rs74415043 | snp | A/G | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98713385 | CCAGCCATGTGGGGT[A/G]TAAGTTGTTTCCATT | 317 |
rs74446759 | snp | A/G | 0.0218709 | 0.10226 | intron-variant | APAF1 | GRCh38.p7 | 12:98671755 | ACCAAAGGGAGTGGT[A/G]CGCTAACTATATCAT | 317 |
rs74448404 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643365 | GGGTCTCTTCTAAAA[C/T]TCTATCACTCTGGAA | 317 |
rs74472032 | snp | C/T | 0.264632 | 0.249571 | intron-variant | APAF1 | GRCh38.p7 | 12:98679854 | AGTGGCTGGACCCCA[C/T]GCTCACTCACACACG | 317 |
rs74475256 | snp | C/T | 0.202035 | 0.245356 | intron-variant | APAF1 | GRCh38.p7 | 12:98678796 | TGCAGCCCGGCCAGA[C/T]GTGCACATGCTTGGG | 317 |
rs74485890 | snp | G/T | | | intron-variant, missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98703481 | GGCAGTGGTTGCTTT[G/T]TCCCAGTACTGTGTA | 317 |
rs74501925 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98701003 | TCTTTGTTTTTTTTT[C/T]TCTTACAAACCAGTG | 317 |
rs74536771 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98667125 | GTATTTTTTTTTTTT[G/T]GAGACAGGGTCTTAC | 317 |
rs74552945 | snp | A/T | 0.000256655 | 0.0113253 | intron-variant | APAF1 | GRCh38.p7 | 12:98662440 | ATTAGTGATTAATAT[A/T]TTTTTTTTAAATTAG | 317 |
rs74560839 | snp | A/T | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98727562 | AAAAAAAAAAAAAAA[A/T]ATCTGGCAGTAAAAT | 317 |
rs74575585 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98687449 | CATTTTGTTTCAAGC[A/G]TATGTTCATAAAATA | 317 |
rs74585090 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98674101 | CTTGGGCTCAAGCAA[A/C]CCTCCTGCTTCAACC | 317 |
rs74618286 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646381 | TGCCCCTGCTGGGCA[C/T]TTTGTAAGCCTTGAC | 317 |
rs74619561 | snp | A/G | 0.121369 | 0.214369 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645405 | AAGACTTGAGGTGCC[A/G]CAGCGGCATCCGGAG | 317 |
rs74630492 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | APAF1 | GRCh38.p7 | 12:98722712 | TGGGGGATAGCTGAG[A/G]TATTTGAAGCTTGGG | 317 |
rs74642378 | in-del | -/TT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98715087 | TCTTTTTTTTTTTTT[-/TT]GGAGGGCAAGCCCAG | 317 |
rs74727546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98651075 | TTGGAACAGGTTTTA[A/G]CTACTTTGTTTTGAG | 317 |
rs74747398 | snp | C/T | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98663536 | CAGTTTTTTGTGTAC[C/T]TTTTATTTGTTGTAT | 317 |
rs74773501 | snp | C/G | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98684490 | TGTCTCCTCCTCCTC[C/G]TCCCTCCTCCTCCCC | 317 |
rs74777180 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98667126 | TATTTTTTTTTTTTT[G/T]AGACAGGGTCTTACT | 317 |
rs74842747 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98696636 | CTGTACTCGCCTGTG[A/C]TTGAAACTTGGGAGT | 317 |
rs75011174 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664204 | TTGTAGTTTTAGTAG[A/C]GATGGGGTTTCATCA | 317 |
rs75026831 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684508 | CCTCCTCCTCCCCCC[A/C]CCCCCCCTCTCATTC | 317 |
rs75126458 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | APAF1 | GRCh38.p7 | 12:98701670 | GGAAGATAATTTTAT[A/G]TTGCATGAAATGCCT | 317 |
rs75137293 | snp | G/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98644151 | GGGTGGGGCAGATGT[G/T]TCCCGGAATGGGGCA | 317 |
rs75170480 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | APAF1 | GRCh38.p7 | 12:98664822 | CTACAGACACATGTC[A/G]CCACACCCAGCTGGA | 317 |
rs75190853 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98709467 | AGCAGATGCCCTAAG[A/G]AGCACTGGAATTCAA | 317 |
rs75377389 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | APAF1 | GRCh38.p7 | 12:98650978 | CTACATTATTGTGAT[G/T]AATTTTCAATTCTAG | 317 |
rs75549713 | snp | A/C | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690824 | ATTCAAAGGATTAAA[A/C]CCATCCACCAAGAGT | 317 |
rs75579173 | snp | C/T | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646339 | ATGAGAGTTTTGATT[C/T]GAATCAATAACTTTT | 317 |
rs75579867 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | APAF1 | GRCh38.p7 | 12:98663081 | TCTGCTGTTAGAGTT[A/C]AAAATAGAGTGAGAA | 317 |
rs75622772 | snp | A/T | 0.00810009 | 0.0631224 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666331 | CAAGTAGATTTTCTT[A/T]CAGAGAAGAATTGCA | 317 |
rs75666371 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | APAF1 | GRCh38.p7 | 12:98650157 | CTCTGTATGACACTT[C/T]TAGGGGAATTCAAAG | 317 |
rs75766418 | snp | A/G | 0.206642 | 0.246211 | intron-variant | APAF1 | GRCh38.p7 | 12:98661649 | CCTGGCTAATATTAT[A/G]TTAGAGACGGGGTTT | 317 |
rs75802049 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98693230 | TGGCTCTCAGCTTTA[A/G]TGTTATTGATGTACA | 317 |
rs75854369 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98699718 | CATGGTTCTTTGGAA[A/C]TGTGCTCCGTGAGAT | 317 |
rs76114477 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | APAF1 | GRCh38.p7 | 12:98681423 | TGGCTTCTACCAGGA[A/G]CATTTATACTAATAT | 317 |
rs76116877 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98666453 | AGATAGTTTCTGTGC[A/G]TAAGTCCTTCACCTA | 317 |
rs76211385 | snp | A/G | 0.206947 | 0.246265 | intron-variant | APAF1 | GRCh38.p7 | 12:98699059 | CATTCCTGGCACAGC[A/G]GAGGGCAGCAGTGGC | 317 |
rs76259518 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | APAF1 | GRCh38.p7 | 12:98725606 | GCACTGTTCACAGTG[A/G]GGACCTTTGTTCACG | 317 |
rs76302028 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98682816 | ACCAGAAATCTATTA[C/T]GCTAACCTCTTTAAA | 317 |
rs76325208 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | APAF1 | GRCh38.p7 | 12:98722743 | AACTCTTGTGTTTTG[A/G]TTTGAAGCTGCTTTG | 317 |
rs76362318 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98689533 | CTTTGTCACCCAGGC[C/T]GGAGTGCAGTGGTCT | 317 |
rs76370671 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | APAF1 | GRCh38.p7 | 12:98669092 | ATATATTTACATTTA[A/G]TAGTGTATATTGGAA | 317 |
rs76371171 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | APAF1 | GRCh38.p7 | 12:98658639 | AGTTATATGTTCCAG[A/G]ACATCAGTAGTTCTC | 317 |
rs76396995 | snp | A/T | 0.180702 | 0.240204 | upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98645103 | AACGCGGCGCGTCCC[A/T]GAGGCTTAGCCACGC | 317 |
rs76466875 | snp | C/G | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98704770 | GACTTTGAATTGGAA[C/G]TGTTTTGTTTTGTGT | 317 |
rs76602498 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98703686 | TTTATTATTTTAACA[A/G]TGATTGCAGACTTGA | 317 |
rs76611271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98696981 | ATGAAAATCATAAAC[A/G]TATGAAGACAGTGCT | 317 |
rs76680641 | snp | A/G | | | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649636 | ATGGCAGGCTGTGGG[A/G]AGTCTGTATTAGCTG | 317 |
rs76709270 | snp | G/T | 0.00010614 | 0.00728415 | intron-variant | APAF1 | GRCh38.p7 | 12:98723621 | TCAACCTCCAAGTGT[G/T]TTTTTTTTTTTTTTA | 317 |
rs76711301 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98667114 | TATATATATATGTAT[A/T]TTTTTTTTTTTGAGA | 317 |
rs76732147 | snp | A/G | 3.295e-05 | 0.00405881 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667544 | TAATCACTCAGTTTC[A/G]GAGATATCACCAGCC | 317 |
rs76742622 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | APAF1 | GRCh38.p7 | 12:98701701 | TGTTTTAAAAATCTG[C/T]ACAGCAGTTCCCTGT | 317 |
rs76787622 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | APAF1 | GRCh38.p7 | 12:98666105 | GGGCTTTAAGATACC[A/G]TTTTTTTGTGTGTGT | 317 |
rs76871446 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | APAF1 | GRCh38.p7 | 12:98721886 | TTCTGCTGTTTAGCA[C/T]TGGCCAATAAAAAGC | 317 |
rs76878990 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643815 | CATAATGATATGGTT[C/T]TCTTTTTTTTTTTTT | 317 |
rs76945651 | snp | G/T | 0.0215338 | 0.101505 | intron-variant | APAF1 | GRCh38.p7 | 12:98723624 | ACCTCCAAGTGTTTT[G/T]TTTTTTTTTTTAAGG | 317 |
rs76975087 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98674312 | TATTTTAAATAATAC[A/G]TTCCTGATTAAGACA | 317 |
rs76998785 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | APAF1 | GRCh38.p7 | 12:98693777 | TTTCTTTTAAATTGG[A/G]ACACTTGTTTTTCAG | 317 |
rs77001512 | snp | G/T | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98686172 | TCCAAACAAACTTTA[G/T]GTAGCATTTGTTCTG | 317 |
rs77058764 | snp | A/T | 0.029116 | 0.117091 | intron-variant | APAF1 | GRCh38.p7 | 12:98668611 | GGTAGAATCATCATG[A/T]TTTGCTTATGGGTTT | 317 |
rs77103840 | snp | C/G | 0.254385 | 0.249962 | intron-variant | APAF1 | GRCh38.p7 | 12:98716282 | CTTTTTTCCGCCTTC[C/G]ACCTGTCCTGCCTTC | 317 |
rs77108372 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98690612 | TTGCCAAATGTTCAA[G/T]AAAGCTGTAAAACTA | 317 |
rs77124339 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98647726 | TTTTTTTTTTTTTTT[C/T]AGCAACAGTATTATG | 317 |
rs77127123 | snp | A/C/T | 0.00338806 | 0.0410194 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715542 | CAAGTTCTGATGATG[A/C/T]TGAAATTCAGGTGAG | 317 |
rs77147874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698508 | TTACCCAGATTACCT[A/G]CAGTTGTTGCAAGTA | 317 |
rs77280378 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98681898 | ATCAGTGCTTTGATA[A/G]CATACAAAGGAAATG | 317 |
rs77296419 | snp | C/G | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98652990 | TTTCCTGGGTGTTCT[C/G]AGTAGACGAGAACTC | 317 |
rs77355388 | snp | C/T | 0.00150903 | 0.027427 | intron-variant | APAF1 | GRCh38.p7 | 12:98648519 | CTCTCTGAAGCAGTC[C/T]ACACTTCCTTAAAAA | 317 |
rs77391446 | snp | C/T | 0.208169 | 0.246476 | intron-variant | APAF1 | GRCh38.p7 | 12:98712562 | TTGCTGTGTCACCCA[C/T]GCTGAGTACAGTGAC | 317 |
rs77424512 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98704446 | CATGACTACTGCAAG[C/T]ACTTCTTCAGTGTTC | 317 |
rs77436830 | in-del | -/T | 0.449726 | 0.150364 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647028 | CAAGAAGTCTCTTAA[-/T]ATTAGGACTTCAATG | 317 |
rs77492371 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | APAF1 | GRCh38.p7 | 12:98675005 | TTTAGTTCTTGTTCT[C/G]TTATGAATTGTTGAG | 317 |
rs77609568 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | APAF1 | GRCh38.p7 | 12:98660540 | CTGTTATCAAGTGTT[A/T]CACAGTTTTCATTAG | 317 |
rs77652205 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | APAF1 | GRCh38.p7 | 12:98692727 | AAAGGACATGATTTT[A/G]TTCTTTTTTATGGCT | 317 |
rs77677500 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98701005 | TTTGTTTTTTTTTTT[C/T]TTACAAACCAGTGTT | 317 |
rs77835688 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98705788 | AATGAAGGTTAGATG[A/G]CAGTATTAGTGGAAA | 317 |
rs77954860 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98725195 | CTAAATTAAGGAAGG[A/C]GTGACATTGATCCTT | 317 |
rs77957517 | snp | A/G | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98656254 | AGATAATCTTGGTTA[A/G]CAATTCGGAGTAAAT | 317 |
rs78031307 | snp | A/G | 0.264358 | 0.249587 | intron-variant | APAF1 | GRCh38.p7 | 12:98678303 | TTTGATGGCAGCGGC[A/G]GGCTGCCTGGAGTGG | 317 |
rs78065602 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708159 | ACCATGTTGGTCAGA[C/T]GTCTTGAACTCCTGA | 317 |
rs78092915 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98659756 | AAACTCCATCAGAAA[A/G]AAAAAAAAAAAAAAA | 317 |
rs78095695 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98671308 | GTTCAGTGGTTTTTT[A/T]AAAAAAAGAATGTAT | 317 |
rs78152264 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98701444 | TTTCCACAGCAGCTG[C/T]ACCGTTTTACATTCC | 317 |
rs78224597 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | APAF1 | GRCh38.p7 | 12:98671243 | AATTTGCTTCCTACC[C/G]TACTGGGAAAGTAGG | 317 |
rs78282483 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665480 | TTTCTTAGTAATGTA[A/G]GTAAGTAAGTCGATT | 317 |
rs78380680 | snp | A/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98666747 | CCAAATTTGGTTTTG[A/T]GTGATGTTTTTCCTG | 317 |
rs78489365 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | APAF1 | GRCh38.p7 | 12:98674705 | GTTGTGTATCATAAG[A/G]GGAAAGTTATTTAAC | 317 |
rs78492828 | snp | A/G/T | 0.000166483 | 0.00912234 | intron-variant | APAF1 | GRCh38.p7 | 12:98699590 | TACTTTAAAAAGCCA[A/G/T]CTTCAGTCTGATTTA | 317 |
rs78511607 | snp | A/T | | | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98647028 | CAAGAAGTCTCTTAA[A/T]ATTAGGACTTCAATG | 317 |
rs78596065 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | APAF1 | GRCh38.p7 | 12:98652374 | GACGGTTGGTATGAT[C/G]CAGCTTTGTAATTTT | 317 |
rs78642754 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98699786 | CCGTTTGGGAAATAT[A/G]TTTTGTATTGCTTTC | 317 |
rs78679629 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | APAF1 | GRCh38.p7 | 12:98659438 | TGCCTTTTTCCTGCT[C/G]TTCTATAGGGAGGAT | 317 |
rs78749537 | snp | C/G | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98707329 | GCTTTTCCTTAAGTG[C/G]TTTCTTATATTTGGA | 317 |
rs78771907 | snp | C/T | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98653936 | TTTGTTTCTGTCCTT[C/T]CCAAGATTTCTTTGT | 317 |
rs78787764 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98662161 | GCTTTTTTTTTTTTT[G/T]TTTTGGCACTCAGTA | 317 |
rs78789463 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98688643 | ACCTGGCGAAATTTT[C/T]TTTTTTTTTTTTTTT | 317 |
rs78802781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98682898 | AGAAATGTCATGTGT[C/T]CATGACACTCTAGTT | 317 |
rs78804831 | snp | A/G | 0.000131841 | 0.00811808 | intron-variant | APAF1 | GRCh38.p7 | 12:98723773 | TGCAAAGGTAGGTCA[A/G]TCAATTGAAACCATG | 317 |
rs78829515 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98718544 | GCCTTCTTTTTTATG[A/G]AAATCAAGTTTCCTA | 317 |
rs78870008 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98688135 | TTAGGGAAAAAAGCT[C/T]ATTCAGCCTTCTGAA | 317 |
rs78892251 | snp | A/C | 0.180702 | 0.240204 | intron-variant | APAF1 | GRCh38.p7 | 12:98658856 | AAGTACAAGGTTTAG[A/C]AACTGTGCTGTGCAG | 317 |
rs78913179 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98726211 | ACTTTTAGAAAACAA[A/T]CTTTTTAGGAGGCTT | 317 |
rs78918342 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98709397 | GAGTCCCAAAGATCC[A/G]TTGGCAGAGGAATGG | 317 |
rs78925600 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98675198 | GAAAGGTTTAGGTTG[A/G]TATAAGCTTAAATTT | 317 |
rs78965115 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98679117 | CCTTTTCCAGGCTTG[C/T]CCATGTCTGCCCATG | 317 |
rs79053765 | snp | A/G | 0.128288 | 0.218372 | intron-variant | APAF1 | GRCh38.p7 | 12:98692645 | GTGAGAACTTGTGGT[A/G]TTTGGTTTTCTGTTC | 317 |
rs79070974 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | APAF1 | GRCh38.p7 | 12:98722061 | CCCAACCTTTTTTCT[C/T]TTCTGTTTCTTCTGC | 317 |
rs79089398 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | APAF1 | GRCh38.p7 | 12:98654114 | TTGTGCCCATAGTCA[A/G]GATGTTTAGATTCTT | 317 |
rs79152008 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98664205 | TGTAGTTTTAGTAGA[A/G]ATGGGGTTTCATCAT | 317 |
rs79200230 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643834 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 317 |
rs79290726 | snp | C/T | 0.00386533 | 0.0437918 | intron-variant | APAF1 | GRCh38.p7 | 12:98662581 | TGGGTAAGGATTATT[C/T]GTTTACTTTTTAGTA | 317 |
rs79333195 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98659102 | GCTTAACAGTAAAAC[C/T]ATTTAAAGGAGTACT | 317 |
rs79349771 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98701406 | TTCTTTATTTATTTA[G/T]TTTTCTGAGGAACCA | 317 |
rs79384865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668451 | CTTCATTAAGAGGAT[A/G]AAGCACAGGCACAAA | 317 |
rs79491399 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98728188 | ACTAGCAAGTTGGGT[A/G]TTTAACTTAGTTCTG | 317 |
rs79512170 | snp | A/G | 0.0179118 | 0.0929251 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644717 | GTCTGGAGACCCTAG[A/G]ACGACAAGCCCAGGG | 317 |
rs79517178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674346 | AACAATAGTAATAGG[A/T]TGTAAGATGAAAAGT | 317 |
rs79568598 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | APAF1 | GRCh38.p7 | 12:98698200 | TTTCTTTTTGTTTTT[A/T]AAAATTTTTTTAAAT | 317 |
rs79804889 | in-del | -/A | 0.268995 | 0.249277 | intron-variant | APAF1 | GRCh38.p7 | 12:98710882 | TGAGCCTCAGTTTGT[-/A]AAGGTCCTTTTCATC | 317 |
rs79854935 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98664427 | GAAACTAAAAAAAAA[A/T]TAGAAATTATCCATA | 317 |
rs79944693 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | APAF1 | GRCh38.p7 | 12:98728195 | AGTTGGGTGTTTAAC[C/T]TAGTTCTGTTTTCCA | 317 |
rs79948018 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98693557 | TTGTTTAGTTTTTAT[A/G]TGTGCTTATCTTCAA | 317 |
rs79955712 | snp | A/G | 0.208169 | 0.246476 | intron-variant | APAF1 | GRCh38.p7 | 12:98724730 | GTTCACTAACTGTTC[A/G]TGAGCCTGTCTTTGT | 317 |
rs79988622 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98647391 | CTTGTTTTTTTTTTT[G/T]AGACAGAGTCTCAGT | 317 |
rs80047148 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98710969 | TACTGGGAGTAAATC[G/T]CCTGGTATGTGGTAA | 317 |
rs80101223 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | APAF1 | GRCh38.p7 | 12:98720008 | TACTTGTTATAGGCT[C/T]CCATGACACTGGTGT | 317 |
rs80143132 | snp | C/T | 0.084364 | 0.187256 | intron-variant | APAF1 | GRCh38.p7 | 12:98728908 | TTGGTGTTTTTTTGA[C/T]GTATCTTTTATCTAT | 317 |
rs80188674 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98697417 | TGATTCATTTATATA[A/G]TCTCAAAGTGACTAG | 317 |
rs80321581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98692021 | AACATACCATGCCTC[A/G]AAGTTATTGCACTCC | 317 |
rs80344227 | snp | G/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98725031 | GTACAATTGTCCTCA[G/T]TTTACAGATGCCGTG | 317 |
rs80353625 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | APAF1 | GRCh38.p7 | 12:98684221 | GTTATTGAAAATTGC[C/T]GTCTCCATCCCCCTG | 317 |
rs111232069 | snp | G/T | 0.000625988 | 0.0176806 | utr-variant-5-prime, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648349 | TCAGAGAGAGAAAGA[G/T]CTGAGGGAAGATGGA | 317 |
rs111293527 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98704066 | CCACCCAGTGAAGTG[C/G]TATATTAGTTTTTTC | 317 |
rs111317482 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98680416 | AGGTAGGAAAATCTT[C/T]TCCTCTTGAGTTGTA | 317 |
rs111368810 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | APAF1 | GRCh38.p7 | 12:98720991 | GAAAAAAAAAATTTC[C/G]TTAACATTTCTACAA | 317 |
rs111382335 | snp | A/C | 0.0490535 | 0.14873 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733222 | TCACCACAATCGCTG[A/C]CTCCTGGGTTCAAGC | 317 |
rs111387764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98703944 | AGGATGTTCATTGCC[A/G]GGCACTAATGAATAA | 317 |
rs111410833 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | APAF1 | GRCh38.p7 | 12:98661826 | GTATAATTATGCTAT[C/T]AGGTTTTAGTTATAT | 317 |
rs111411987 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98700202 | GTATTCAAGAAGCAG[C/T]GGGTTACAGTAGCCC | 317 |
rs111495253 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734488 | TAACTGGAACTAAAT[C/G]AAATGATTACTAGTG | 317 |
rs111555994 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98717036 | ATGCCAAGCTAATTT[C/T]TTGTATTTTTTTTAG | 317 |
rs111643962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98665867 | CTGAGCATGTTGTTA[C/G]AGAGAACCTTGGAAG | 317 |
rs111705093 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98690838 | AACCATCCACCAAGA[C/G]TCCCCTATCATAAGC | 317 |
rs111705125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98709591 | CAGCAAGAGAAAGCA[C/G]ATGCCTCATGGAAGA | 317 |
rs111723316 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98649134 | GGAAAAAATAAGAAT[C/T]TTTAGAAATATATGT | 317 |
rs111760682 | snp | C/T | 0.5 | 0 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98683226 | CCATTTCACCAACAG[C/T]AGTCATCATCTTCTC | 317 |
rs111833166 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | APAF1 | GRCh38.p7 | 12:98724969 | GATTACTTGTCACAT[C/G]CTAGTAATTTCACTC | 317 |
rs111857424 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | APAF1 | GRCh38.p7 | 12:98706406 | GGTATTGCTGGCTCA[C/T]TCTTGCTATTTTCAA | 317 |
rs111880910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98682829 | TATGCTAACCTCTTT[A/G]AAGCACTTCTCTGCC | 317 |
rs111885484 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662552 | CAGAGACAAGAGTGT[C/T]ACAGATTCAGTAATG | 317 |
rs111938550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717160 | GGCATGAGCCCCCGC[A/G]CCTGGCCTACTGTGC | 317 |
rs111960050 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98707910 | AGACACAGTTACAGT[A/G]TGTTTAGTGATGTAG | 317 |
rs112021294 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | APAF1 | GRCh38.p7 | 12:98717136 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 317 |
rs112089778 | snp | A/C | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98717155 | TTACAGGCATGAGCC[A/C]CCGCACCTGGCCTAC | 317 |
rs112090662 | in-del | -/AGATA | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98694051 | CTATTCAATAAATGG[-/AGATA]TGCTGGGATAACTGG | 317 |
rs112099215 | in-del | -/C | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98714593 | TGTTATGCTATCCTG[-/C]CCTTGCCTCAGGGTT | 317 |
rs112219060 | snp | A/C | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98652822 | GTAGAGACGGGGTTT[A/C]TCCATGTTGGTCAGG | 317 |
rs112236198 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | APAF1 | GRCh38.p7 | 12:98667822 | TGTTTCTCAGGCTGG[A/T]GTGCAGTGGCACAAT | 317 |
rs112236636 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98718896 | CTATGATCATGCTAC[C/T]GCACTCCAGCCTGGG | 317 |
rs112256212 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | APAF1 | GRCh38.p7 | 12:98724660 | GTTAGCTGCTCTACC[G/T]CCAGTGTTTCTATTA | 317 |
rs112291353 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98683697 | TATTTGACTCATTTT[A/G]GCTTACATGCTCATA | 317 |
rs112353483 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708279 | ATTGGTATCAAACAG[C/T]TTGATAACCAGCAGG | 317 |
rs112358290 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98703652 | CTCTAACTTTGGGAT[A/G]TTAAACCACATAGCC | 317 |
rs112359747 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98697963 | TTGCCATTTAAAGCA[C/T]GCAGAGGCCTGGGGT | 317 |
rs112363625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707805 | TGGTTCTTAACATGC[C/T]AGTCTCAATGAGCTT | 317 |
rs112394296 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | APAF1 | GRCh38.p7 | 12:98720691 | AAGTTTCCAGCCGGG[C/T]GCGGTGGCTCACGCC | 317 |
rs112437685 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98701950 | CAGCCACTAATTTTT[A/T]AAAAAATGACCTATC | 317 |
rs112458209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98669894 | CCCCTCCCCTCCCCT[C/T]TTCCTGCCCTCCCCT | 317 |
rs112537517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98682093 | GAGTCTCGCTCTTTC[A/G]CCCAGGTTGAACTGC | 317 |
rs112599246 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98647426 | CGCCCAGGCTGGAGT[A/G]CAGTAGAGTGGTCTC | 317 |
rs112605025 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98648505 | GAAATGAGGTAAAGC[C/T]CTCTGAAGCAGTCCA | 317 |
rs112605394 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98702501 | AAAAACTTTGGAAGA[C/G]TATATTCAGCATTTA | 317 |
rs112627534 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98682995 | ATATTTTAGAAAGGG[G/T]AGAGGTTTCATTAGC | 317 |
rs112692220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718065 | CATTTAGTATGTACA[C/T]CTTCCCTTGATCCCT | 317 |
rs112694108 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98695933 | GATTTCTCCACTGCA[A/G]GCTCAGAATTTAATT | 317 |
rs112762079 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98663772 | CAAGCAGTTCTTCTG[C/T]CTCAGCCTCTCGAGT | 317 |
rs112771036 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | APAF1 | GRCh38.p7 | 12:98685862 | GGCTGGTCTTGAACT[C/G]CTGACCTCAGGTGAT | 317 |
rs112776504 | in-del | -/AA | 0 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98693066 | TTTTATTTTTTGACT[-/AA]AAAAAAAAAACAACA | 317 |
rs112781829 | snp | C/T | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98690806 | TAATGTTACCTCATA[C/T]CCATTCAAAGGATTA | 317 |
rs112813081 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98656117 | TATTTTTTTAGGGAC[A/G]TGGTTTCACCATGTT | 317 |
rs112844480 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732152 | CTATAGCTTCCTGTC[C/T]GCAGCTCTCAAGCAG | 317 |
rs112850510 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682325 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 317 |
rs112860087 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98704677 | TGCACACAGAGGCAG[A/G]GAGTGTGAAAAAGCT | 317 |
rs112954276 | snp | C/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98694579 | TTAAGTATTCATTCT[C/T]GTGTGATTAGTTCCT | 317 |
rs113017898 | in-del | -/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98666105 | GGCTTTAAGATACCG[-/T]TTTTTTTGTGTGTGT | 317 |
rs113035658 | snp | A/G | 0.000636292 | 0.0178253 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649657 | GTATTAGCTGCAGAA[A/G]CTGTTAGAGATCATT | 317 |
rs113090746 | in-del | -/TAAC | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98677134 | AAGTGACATGTTGAT[-/TAAC]TAGATTTGATTAATT | 317 |
rs113100940 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98664497 | TCTTTTAGAACAAAG[A/T]TTTAAAAAGTTGAGA | 317 |
rs113104589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98660743 | AGCATTCCTTGGGAA[C/T]GTTATAGTATACTGA | 317 |
rs113187761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98660717 | AGTGCTGCAAGTACA[A/G]AGATAAATAAAGCAT | 317 |
rs113191658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98683810 | AATGAGTGAGGTCAA[C/T]TCTACTTGAATCGTA | 317 |
rs113248677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98654315 | AAAAAGGCCTTTGAC[C/T]CTAGGTAATAGGTAC | 317 |
rs113354620 | snp | A/C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735282 | GACTTCATATATATA[A/C/T]TTTTTTTTTACATTA | 317 |
rs113358917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98672564 | AACCCTGATTATTCT[C/G]TCTCTTAAAGGAGTC | 317 |
rs113360522 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98696796 | CCACTGCACCCTGCC[A/G]GGAGTAATCAGTCTT | 317 |
rs113385506 | snp | G/T | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98702942 | TGGAGCAATTTGGTA[G/T]TTCTAGAGAGAAATA | 317 |
rs113403511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98717163 | ATGAGCCCCCGCACC[C/T]GGCCTACTGTGCTCT | 317 |
rs113501222 | snp | C/T | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98687285 | GAGAATTGCTTGAAC[C/T]CGGGAGGTGGAGGTT | 317 |
rs113501353 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643484 | TGGGCTATTCCCTCC[C/T]CCCGCCAGAAAAAAA | 317 |
rs113502567 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98684064 | AACCTTTCTTCCTTG[A/G]TACCATACCATCTTT | 317 |
rs113529464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98674989 | GATCAAAGGGCATAG[A/G]TTTAGTTCTTGTTCT | 317 |
rs113547860 | snp | A/T | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98725398 | AGCATTGCTAAACAA[A/T]CCTAATTGCCTTCCA | 317 |
rs113577911 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645368 | ACCAGAGGTGGGGAG[A/T]CTGGGCAGTCGGCGA | 317 |
rs113613007 | snp | C/G | 0.254105 | 0.249966 | intron-variant | APAF1 | GRCh38.p7 | 12:98695087 | AGATGGAGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 317 |
rs113651043 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98707806 | GGTTCTTAACATGCC[A/G]GTCTCAATGAGCTTG | 317 |
rs113714048 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | APAF1 | GRCh38.p7 | 12:98729220 | TGTAAAAGTGGTAGA[A/T]GATGATACTCTATAT | 317 |
rs113828905 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | APAF1 | GRCh38.p7 | 12:98672817 | TGGAGTGCAATGGCA[C/T]GATCTCCGCTCACGG | 317 |
rs113829829 | snp | C/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98697515 | TTCTTCAAACTCGGA[C/G]ACTTTTTAAAAAGTC | 317 |
rs113858373 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98723827 | GTATAATGAGTTCAA[A/G]TAATATATGCAAAAG | 317 |
rs113907867 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645393 | CGGCGACCCGCGAAG[A/G]CTTGAGGTGCCGCAG | 317 |
rs113963416 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730334 | TTGGAAGCTGGGGAG[A/T]CTTCGGCTATATTAG | 317 |
rs113968613 | snp | A/G | 0.5 | 0 | intron-variant | APAF1 | GRCh38.p7 | 12:98648247 | CTTTTTACGTTTCTT[A/G]TTTATTAGTGAGATT | 317 |
rs113987233 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646006 | GGGGTTTTCGTGGAT[A/G]AACGTGCGCTGTTTT | 317 |
rs114213594 | snp | A/G | 0.00367531 | 0.04271 | intron-variant | APAF1 | GRCh38.p7 | 12:98677387 | GTTACTTTTACTCTC[A/G]TTTATTTAATTTCTG | 317 |
rs114232401 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98683379 | ACTTTCTGGTCACAA[A/T]GATAGAAACTACAAT | 317 |
rs114335874 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98679811 | TGGAGCTGCCTGCCC[C/T]GCTGCAGCAGTCAGC | 317 |
rs114387314 | snp | C/T | 0.452227 | 0.146984 | intron-variant | APAF1 | GRCh38.p7 | 12:98724736 | TAACTGTTCGTGAGC[C/T]TGTCTTTGTGATTAA | 317 |
rs114579712 | snp | C/T | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98700943 | AGAACTGTATTTCTT[C/T]TTATGGCTGAATAAT | 317 |
rs114713788 | snp | A/G | 0.030278 | 0.119257 | intron-variant | APAF1 | GRCh38.p7 | 12:98664914 | ATTTACCAGTGGCAT[A/G]ATATTGATATATCTT | 317 |
rs114825860 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | APAF1 | GRCh38.p7 | 12:98674128 | AACCTCCTGAGTAGC[C/T]GAGACTACAGGCACA | 317 |
rs114977763 | snp | C/T | 0.030278 | 0.119257 | intron-variant | APAF1 | GRCh38.p7 | 12:98712786 | CCCAAAGTGTGGGGA[C/T]TATAGGCATGGGAGC | 317 |
rs115155998 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | APAF1 | GRCh38.p7 | 12:98686265 | TTGATTTATTAGAGC[A/C]ATTTAGTCATTTGTC | 317 |
rs115185919 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98658919 | AACTTTACTTGGTAA[A/G]ATTTTCCCGATAAGC | 317 |
rs115296011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98716801 | ATTCAGATGTTAGAT[C/T]TCCCGGACTGATAAT | 317 |
rs115297386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98724473 | TCACCATCTTTTTCT[A/G]CTATATTGTTTCCTC | 317 |
rs115502224 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98674543 | CCCATATCATAGGAT[C/T]TGTCACACTTTATAG | 317 |
rs115567249 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98653967 | GTTATTAGATTATTA[A/G]TTGCTACCAGGATAA | 317 |
rs115701358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652441 | TTGCATTTCTCTGGT[A/G]ACTCAAGTTTGAACA | 317 |
rs115702150 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98722673 | AACAATGCCTTCTCA[C/T]TTCCGTCATTTTGAG | 317 |
rs115729180 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98714578 | GGCTGTGTGCTCAAC[C/T]GTTATGCTATCCTGC | 317 |
rs115805629 | snp | G/T | 0.0573587 | 0.15934 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732992 | ACACTTACCCCAAGG[G/T]GGTTTTGTTCTCCTA | 317 |
rs115826246 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | APAF1 | GRCh38.p7 | 12:98703892 | GGTGAGAAATGAGTC[C/T]AGTTCAGATTTCTTA | 317 |
rs115984314 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98656147 | TGCTCAGGCTGGTCT[C/T]GAAATTCTGGGCTCA | 317 |
rs116039326 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98696895 | ACCCTGAAAAAGAAA[A/G]AAGTATACTTCCTGG | 317 |
rs116205465 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | APAF1 | GRCh38.p7 | 12:98679169 | TCCCTTCTGAAGCCC[A/G]TAAAAGCCTCGGGCT | 317 |
rs116289685 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735211 | TTGTAGTTTGCAGAT[A/G]AGCATTTCTAAAGCA | 317 |
rs116426123 | snp | A/G | 0.452227 | 0.146984 | intron-variant | APAF1 | GRCh38.p7 | 12:98724738 | ACTGTTCGTGAGCCT[A/G]TCTTTGTGATTAAAC | 317 |
rs116501350 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645337 | TGACTGCTCTATCCC[A/G]GGCAAAAGGGATAGA | 317 |
rs116514277 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98673600 | GAAGTCCAGGTTGGT[A/G]TCTGTGATCTTTATG | 317 |
rs116565057 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98688929 | ATGATCCTCCCACCT[C/T]AGCCTCTTGAGTAGC | 317 |
rs116591662 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98657761 | TGAATCTCAACTCTG[C/T]TTCATTAGCTGTGTA | 317 |
rs116593758 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | APAF1 | GRCh38.p7 | 12:98721979 | ATTCTTTTGGAGCTG[A/G]CCTGTTTTCCCATAC | 317 |
rs116624926 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | APAF1 | GRCh38.p7 | 12:98691730 | TTTTTTTGTTTTTTT[A/G]TGTTTTTTTTGAAAC | 317 |
rs116626329 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98701728 | CTGTTTTACCATGCT[A/G]AAAGAAAGCTACCCA | 317 |
rs116674040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661450 | TTTCAACCTATGTAT[A/G]TGCCTAGAGTATTTC | 317 |
rs116676922 | snp | C/T | 0.452227 | 0.146984 | intron-variant | APAF1 | GRCh38.p7 | 12:98724735 | CTAACTGTTCGTGAG[C/T]CTGTCTTTGTGATTA | 317 |
rs116702561 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | APAF1 | GRCh38.p7 | 12:98679650 | TCCCCAAGCTAGGGC[A/T]GTGACTCCCTCTTTG | 317 |
rs116884285 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733132 | ATTTAGCAGGCCCCC[C/T]CACCTTTTTTTTTTG | 317 |
rs116928965 | snp | A/G | 0.0452528 | 0.143452 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735094 | CTTAAAAGAAAAATG[A/G]GAAGAAAGACAAGGT | 317 |
rs116988718 | snp | C/T | 4.94474e-05 | 0.00497205 | intron-variant | APAF1 | GRCh38.p7 | 12:98723188 | CTTATTTCTTTGATA[C/T]TCAGGTATGGAATTG | 317 |
rs117067507 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98707438 | AGAATGCCTGTCTCT[C/G]TTAATGCCATCTAAT | 317 |
rs117069060 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98665911 | GGACTGAGGTGGTGG[A/G]GTGTTGGGTGTAGAA | 317 |
rs117101956 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98692430 | CTTTTATTTAGATTC[A/C]GGGGTACATGTGCAG | 317 |
rs117104034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98703554 | GAGATCAAAGGATGA[C/T]AGAGAATGGGCAGCT | 317 |
rs117235066 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98660604 | TCTTAAGAGTATAAC[A/C]TTGGATTCAGTCAAC | 317 |
rs117235991 | snp | A/C | 0.0198392 | 0.0976012 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699448 | AGAGGAAAAGCATTA[A/C]TGTGAAACAGTTCTT | 317 |
rs117359388 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98687611 | AGAGAGTGAGGAGGC[A/G/T]GCTGAACTTATCCAT | 317 |
rs117452856 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98701746 | AGAAAGCTACCCAAA[G/T]GTGTTCCTTAACTGC | 317 |
rs117466473 | snp | A/T | 0.116138 | 0.211142 | intron-variant | APAF1 | GRCh38.p7 | 12:98652635 | ATTTTATTTTATTTT[A/T]TTTTTTTTGAGACGG | 317 |
rs117592012 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98700621 | TGTGATAAAATGCAT[A/G]TAATGTAAAAGTTGC | 317 |
rs117629149 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | APAF1 | GRCh38.p7 | 12:98689199 | TTCTAAGGTTCTTCA[C/T]CTTCCGTCATTCTGC | 317 |
rs117670652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98726649 | ATTTTGCTCTGAGTT[C/T]GCGTCTTTGGATGAA | 317 |
rs117751447 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | APAF1 | GRCh38.p7 | 12:98692819 | AGGTTGGTTTGTGTC[C/T]TTGCTGTTACGAATA | 317 |
rs117770849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98729123 | ACAAAGGAGAGGAGT[A/G]ACCAGACCAACCTCA | 317 |
rs117808368 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98713743 | TTATTTTTTAACCAA[A/T]TACTTATGGCACTGG | 317 |
rs117894982 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732290 | ATTCAGCATTAAATC[C/T]GAGACATTTTCCTCC | 317 |
rs117962329 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646705 | TAGACTCTTTCACTC[A/T]ATACATTGTGTAAAG | 317 |
rs117974213 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98657406 | CTATGCTGGGAAGTG[C/G]AATAGGTATTTGCTC | 317 |
rs118005084 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | APAF1 | GRCh38.p7 | 12:98709532 | AAGGTGTCGTTGCAT[C/T]GACAGAGATGTCCTG | 317 |
rs118043459 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98713730 | AGGTGTCTGGGAATT[A/G]TTTTTTAACCAATTA | 317 |
rs118102803 | snp | C/T | 0.00772225 | 0.0616562 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732569 | GACTTTAGAATAAAA[C/T]AGTTAAGCATTAATG | 317 |
rs118113879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98677159 | TGATTAATTTGATTA[A/G]TTAGATTTCTTCCAA | 317 |
rs137869499 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98703285 | TCATATTTTTTTCAG[A/G]ACTTATATTTGAAAT | 317 |
rs137933277 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98649915 | AAGTTAGCTAGGCAG[G/T]GAAGGTAGGGATGGG | 317 |
rs137935495 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98694974 | GGTGAACTTTTGATG[G/T]CAAAGTCTTTATATC | 317 |
rs137940277 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98690658 | GTACAAATATAAGTT[G/T]TACAGCTCAGCTGGG | 317 |
rs137983508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98661128 | GGATGGTCTTGATCT[C/G]CTGACCTCGTGATCT | 317 |
rs137988298 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735849 | GGTGGTATGTACAAG[C/T]GGAGGGGAAGGGGTT | 317 |
rs138060614 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98704137 | GTGCTTTTTTTTTTT[-/G]TTTTTTAATAGAAAT | 317 |
rs138067541 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98653195 | ATCTCTGGAGTTCAC[G/T]TCCATTCTCAAATAC | 317 |
rs138068283 | snp | C/T | 1.65045e-05 | 0.00287263 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98686785 | AATGTCGAAATACCA[C/T]GTTTGGTCATACAAA | 317 |
rs138084893 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98653080 | GTTCAAGTAGTCCTA[-/T]TTACAGTCTTATTAT | 317 |
rs138085252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689230 | CACATCCTTTCCTGT[C/T]AAGTTTGTTTCTTCT | 317 |
rs138126255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98711627 | TTATGACACTAAGAG[A/G]GAGGTATCTGACAAC | 317 |
rs138148311 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98656831 | TTCTTGCTCTCTGTT[G/T]TCTCATCCAGACCAT | 317 |
rs138188210 | snp | C/T | 0.00330665 | 0.0405264 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98725431 | TCTGGAGTTTTGATC[C/T]CCTTTTGCCACTTCA | 317 |
rs138197021 | snp | A/G | 0.022942 | 0.104618 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644732 | GACGACAAGCCCAGG[A/G]CAGCTTCTTCACCAG | 317 |
rs138315125 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98676335 | ATGCCTCAGCCTCCC[A/G]AGTAGCTAGGATTAC | 317 |
rs138329204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98672438 | CCAAAGTGCTGGGAC[C/T]ACAGGCATGAGCCAC | 317 |
rs138330341 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98685316 | ATCAGTATTTTGTCA[A/G]TCTTATTTTATAAAT | 317 |
rs138330961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98666477 | TCACCTAGCTTCCCC[A/T]AATATTAACATTTTA | 317 |
rs138431329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98686567 | GCTGATCTAAAGGCT[A/G]CCCCATTGCTTGTTA | 317 |
rs138460842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98698667 | AGCCTGAGCAGCAGC[G/T]TTCTCCCCCAACCCC | 317 |
rs138526583 | snp | A/G | 0.00731647 | 0.0600392 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699432 | GCGACATCAGCAAAT[A/G]AGAGGAAAAGCATTA | 317 |
rs138571218 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731586 | TAGTGAACATGCTTA[C/T]TTGACCCACTCACAT | 317 |
rs138584854 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98657428 | TATTTGCTCCTCAAG[C/G]CTTCATCCAGACCAT | 317 |
rs138594575 | in-del | -/ATA | | | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665276 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 317 |
rs138616141 | snp | A/G | 8.33785e-05 | 0.00645618 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662715 | GAGTTCCTTAGGAAA[A/G]GAAAAAGGACTTGAA | 317 |
rs138619900 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | APAF1 | GRCh38.p7 | 12:98727966 | AATAAATAAATAAAT[A/T]AATTAATTAATTAAT | 317 |
rs138638140 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98652361 | CTACTTGTGCAGTGA[C/T]GGTTGGTATGATCCA | 317 |
rs138686057 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665447 | CTTAAGGCTTTTGAT[A/G]ACATGCAGCAGAAAT | 317 |
rs138865151 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98710844 | ACTAGTTCTATGATG[C/T]TGAATAAATTGTATC | 317 |
rs138872414 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98708198 | GATCTACCCGCCTTG[G/T]CCTCCCAAAGTGCTG | 317 |
rs138910177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98671404 | ATTTGTTACTTAATG[A/G]TTGGCTGTTCAATTT | 317 |
rs138929176 | snp | C/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98681490 | CACTGATATATGGAA[C/G]ACAGACCTTACTTTA | 317 |
rs138939479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98722241 | AATGTGCTATCTCCA[A/G]ATTTTCTCTAAGGAA | 317 |
rs138987646 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98714733 | CTCCTGCTTTAGCAT[A/C]ATCTGTATTTTCCTT | 317 |
rs138996945 | snp | A/G | 0.206336 | 0.246157 | intron-variant | APAF1 | GRCh38.p7 | 12:98720860 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 317 |
rs139016212 | snp | C/T | 0.000164794 | 0.00907577 | stop-gained, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723229 | AAATGTATCTTTCTA[C/T]GAGGCCATCAGGAAA | 317 |
rs139060875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98687010 | AGGAGCATATTTAAT[G/T]TAACTGTAATTGCTT | 317 |
rs139072016 | snp | C/T | 0.000790653 | 0.0198671 | intron-variant | APAF1 | GRCh38.p7 | 12:98648866 | CAAAATTGCTTTGGG[C/T]TTGTCTTATTGTAGA | 317 |
rs139083690 | snp | A/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699501 | GAGGATATGGAAGTG[A/T]TAGTGAAGTGTTGTT | 317 |
rs139121628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98709011 | ACAAGAGTGATTCAG[A/T]CATGTCTGATGGAGT | 317 |
rs139274870 | snp | A/C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649497 | TTTAGTAAGGACAGT[A/C/T]CTGTGTGAAGGTGGA | 317 |
rs139293553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658403 | CATAACACTAATAAC[C/T]TGTTTTAATCCTTTA | 317 |
rs139326503 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | APAF1 | GRCh38.p7 | 12:98701159 | ATTTATGTATATAAT[A/G]GGCTTAATTATTTAA | 317 |
rs139343359 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98706795 | TTCGTTACATGTTCA[C/T]TGAGGATTACCATGG | 317 |
rs139345050 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98661411 | TTAATCTCTCAGTCT[C/T]ATTTGGTTTGTGCTT | 317 |
rs139378273 | snp | C/G/T | 0.000264055 | 0.0114874 | missense, synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666345 | TACAGAGAAGAATTG[C/G/T]AGCCAGCTTCAGGTA | 317 |
rs139396408 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98702000 | TGATTTCCTGCCCTG[C/T]GTTTTTGGCCTCCGG | 317 |
rs139401961 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98728030 | AAAAAGGCAGTTACT[A/G]TTATCCCCATTTTGT | 317 |
rs139448516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98679269 | TTGCTGAGAGCTGTG[C/T]AGATGACAGGAGGAC | 317 |
rs139536814 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98678035 | AATGAGTACTTTTCT[G/T]TATGTTTGTGTTCTG | 317 |
rs139550753 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | APAF1, IKBIP | GRCh38.p7 | 12:98645592 | CGTTGGGTGGACGCC[C/G]ACCTCGCCAACCTTC | 317 |
rs139629204 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98682462 | GCAGGGTTAAGTGTC[A/C/G]ATCCCGTTTACAGAA | 317 |
rs139660301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704947 | AGCATGCCCGGCTAA[G/T]TTTTTTTTGTATTTT | 317 |
rs139683823 | in-del | -/TTA | 0.453818 | 0.144769 | intron-variant | APAF1 | GRCh38.p7 | 12:98724737 | ACTGTTCGTGAGCCT[-/TTA]GTCTTTGTGATTAAA | 317 |
rs139749004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98683524 | TGTGTTCTCAGGCTC[C/T]ACCTCCCTTTCCATC | 317 |
rs139782973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98723824 | TATGTATAATGAGTT[C/T]AAATAATATATGCAA | 317 |
rs139786967 | snp | C/T | 6.59044e-05 | 0.00574002 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723719 | TTGTGACATTTCTCA[C/T]GATGCTACCAAGTTT | 317 |
rs139788089 | snp | A/G | 0.00121081 | 0.0245751 | intron-variant | APAF1 | GRCh38.p7 | 12:98662811 | AGAATGTAAAGGTAT[A/G]GTTATTTATTTGTTT | 317 |
rs139795949 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98650606 | AGACTTAGAAATATG[C/G]AGGCTAGGGTATATC | 317 |
rs139940389 | snp | A/G | 0.000757488 | 0.0194466 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706504 | GGAATACAGACTCAC[A/G]TTCAAAGGTGGCTGA | 317 |
rs139951279 | snp | A/C/T | 3.30656e-05 | 0.00406595 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648758 | CTTCTCCATGATGGC[A/C/T]TTCCTGTTGTCTCTT | 317 |
rs139960385 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98663720 | CTGGAGTGCAGTGGC[G/T]TGATCTCGGCTCACT | 317 |
rs139964896 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98733981 | TTCTCCACTGCTAAA[C/T]GTTAGTCATTGAGGT | 317 |
rs139966250 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98692340 | CGCCTGCCTCGGCCT[C/G]CCAAAGTGCTGGGAT | 317 |
rs140029024 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98729043 | GGGGAAGCAGGTGGT[A/G]AACCAATAAAGTCCC | 317 |
rs140030216 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733474 | GTCTTGCACTATCAC[C/T]CAGGCTGGAGTGCAG | 317 |
rs140151475 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98727244 | AGGAGCTGCTACCCA[C/T]GGAGGCTGGGTGACT | 317 |
rs140171862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646782 | ATGCCCATGGAAAAA[C/T]TTGCATTATATTTGA | 317 |
rs140174192 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | APAF1 | GRCh38.p7 | 12:98718648 | GAGGCATTAAAAATA[C/T]GGCCTTACTGGGCGC | 317 |
rs140202028 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | APAF1 | GRCh38.p7 | 12:98695543 | CTAGAAGAAATTTTA[A/G]TCTCCTATTTGTAGG | 317 |
rs140245163 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | APAF1 | GRCh38.p7 | 12:98702680 | AAATAAAAAAATTAG[C/G]TGGGCGTGGTGGTGC | 317 |
rs140313256 | in-del | -/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98678320 | CTGCCTGGAGTGGCT[-/G]GCTGCCATCATGCTG | 317 |
rs140318784 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98694944 | CTGTGGCACCATCTC[A/C/G]GCTCACTGCAAGATG | 317 |
rs140327382 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677550 | CTGATAAAACCTTAC[A/G]GGTAAAACACATCTC | 317 |
rs140352209 | snp | C/T | 0.0260105 | 0.111035 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98735419 | ATAAAATTCACAAAA[C/T]TGTTTTGAAAAACAT | 317 |
rs140383110 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98713154 | AATAAATCTTTCTGT[G/T]ATCTATTAGTCATTG | 317 |
rs140386258 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98656608 | TCTTCTGTCATTCCT[A/G]TGTGTTTCTGCCATA | 317 |
rs140447354 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98709099 | TGAAAGAACAGAAGT[C/G]ACTTTAGGTGAGGAA | 317 |
rs140453549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98694005 | ATGCATAGTTTAACA[A/G]GGCCAACAAAAGCAA | 317 |
rs140473803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674304 | GCAGGTTTTATTTTA[A/G]ATAATACATTCCTGA | 317 |
rs140491790 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98687850 | ACAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTA | 317 |
rs140537329 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98648227 | GAAAAAAAATCAGTT[A/T]TGTTCTTTTTACGTT | 317 |
rs140629032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98707064 | GCCACAAGTCTTCTT[C/T]CTTGCTTTTCTGCAT | 317 |
rs140641536 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98719330 | GAGTTCATAATGCCG[A/G]TTTTGTTGCTTTAGA | 317 |
rs140641858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675466 | CGACCCTCCATATCC[A/G]TGGTTCTATATCCAT | 317 |
rs140675171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98715829 | ATTTGGATTTGTATC[A/G]GTAAGTATACTTTTT | 317 |
rs140746213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98679883 | CGCCTCGCTGTTCCA[C/T]GCCTGACTCGCCCTT | 317 |
rs140772800 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666254 | TGCAGGAGTTTGTAA[A/G]TAAGTCTCTTTTATT | 317 |
rs140799322 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98695881 | GCCAGCACTTCCTGA[A/G]TCTTTTTGGAGTTCT | 317 |
rs140836008 | snp | G/T | 0.00199806 | 0.0315443 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712338 | TTAATGGAAGAACAG[G/T]TCAGATTGATTATCT | 317 |
rs140890103 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | APAF1 | GRCh38.p7 | 12:98656074 | AGGCATGAGCCACCG[C/T]GCCCGGCCTTGCCTG | 317 |
rs140891416 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | APAF1 | GRCh38.p7 | 12:98700367 | GAATGAGGGATATTA[C/T]TGTTTTAAAGAGCAT | 317 |
rs140896989 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734542 | ATTGTTGGTGCATAT[C/T]AGTATAACTGTGGGG | 317 |
rs140946023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98729334 | GGGAGCGGGGAATGG[A/T]TTCAGGATTAAACTG | 317 |
rs140961577 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98657010 | TTGATACCTGTGTGG[A/T]TGAGTCATCCAAAAC | 317 |
rs141017719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684015 | CCAGAAAGATCTGCT[A/G]ACTTTTTTTGAATTG | 317 |
rs141029437 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98698254 | GATGAGGTCTCACTG[C/T]GTTGCCCAGGCTGGT | 317 |
rs141030439 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98657804 | TTACTCAACTTTTCT[A/G]TTCTTCAGTTTCCTC | 317 |
rs141051658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98725678 | ATTCTTTTTGTTTCT[G/T]GTGCACATTGTATTC | 317 |
rs141077961 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98670061 | GTGATCCTTCCACCT[C/T]AGCCTCCTGAGTAGC | 317 |
rs141157255 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659331 | GCATTCTGATGCTTC[A/G]CAAACACCCAAGGTA | 317 |
rs141162050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695119 | GTGCAGTGGCGTGAT[C/T]TCAGCTCACCACAAC | 317 |
rs141234943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98649805 | TACAGAGTTAGAACA[A/G]AGGAAGGATATGTTA | 317 |
rs141253527 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | APAF1 | GRCh38.p7 | 12:98722683 | TCTCACTTCCGTCAT[C/T]TTGAGGATTGCGATG | 317 |
rs141273503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98674512 | AGATCTGTCTGTATT[C/T]GAGAGAACTGTTTGC | 317 |
rs141328519 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98710634 | TCACTATGTTGACCA[C/T]GCTGGTCTTGAACTC | 317 |
rs141352935 | snp | C/T | 0.000115742 | 0.00760641 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648761 | CTCCATGATGGCATT[C/T]CTGTTGTCTCTTCTT | 317 |
rs141394021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98681264 | ACAGAGTTTTGCCAT[A/G]TTGGTCAGGCTGGTA | 317 |
rs141422750 | in-del | -/AT | 0.0584853 | 0.160693 | intron-variant | APAF1 | GRCh38.p7 | 12:98650912 | TTGTGTATTTATAAT[-/AT]TCCAATTTATAGGTT | 317 |
rs141444986 | in-del | -/CT | | | intron-variant | APAF1 | GRCh38.p7 | 12:98695391 | AGACAGGGTCTCACT[-/CT]GTCACACAGGCTGGA | 317 |
rs141477813 | snp | G/T | 0.204496 | 0.245824 | intron-variant | APAF1 | GRCh38.p7 | 12:98715234 | AGGCATACATGGTGT[G/T]CATATATATATATAT | 317 |
rs141494029 | snp | C/G/T | 0.00319034 | 0.0398225 | intron-variant | APAF1 | GRCh38.p7 | 12:98652199 | CTCAAGTGATGCTCC[C/G/T]GCCTTGGCCTCCCAA | 317 |
rs141502272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98726123 | TTATTACCCTGCAGT[A/G]CTTAAGATATACATA | 317 |
rs141521987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98700829 | TGCGAATTTGCCTAG[A/G]TATTTCATATAAATG | 317 |
rs141569889 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | APAF1 | GRCh38.p7 | 12:98722076 | CTTCTGTTTCTTCTG[C/T]GTCTCCTATGCTCTA | 317 |
rs141640862 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98657716 | GTGGATGCAGAATAG[G/T]GTAGAAGTTGAACAT | 317 |
rs141674878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98686610 | TTTTTGTGTTTGATA[C/T]GTTTGTGTTACTGTG | 317 |
rs141675057 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731856 | TACAGCCCTTGCTAC[A/G]TTTGAGATGTTCAGT | 317 |
rs141686387 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98656510 | CTCAGTTACTGTAGA[G/T]TTCTCTGTCTCCAGT | 317 |
rs141729480 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | APAF1 | GRCh38.p7 | 12:98685880 | GACCTCAGGTGATAC[A/G]CCCACCTCAGCCTCC | 317 |
rs141735706 | snp | A/C | 0.0861826 | 0.188849 | intron-variant | APAF1 | GRCh38.p7 | 12:98727785 | GTCTCTACTAAAAAT[A/C]CAAAAAATAGCCGGG | 317 |
rs141767256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689930 | TGTTTCTTTGATTAG[A/G]TTGAATATAGGTTTA | 317 |
rs141824871 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665723 | AGTGTTGAAATGCTC[A/G]GAGAAGACATCAAAG | 317 |
rs141911270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704234 | TGGCCTCCCAAAATG[C/G]TGGGATTACAGGTGT | 317 |
rs141918026 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98706272 | TCAGTTGGTTCCCTA[C/T]TGATGAGTATTTAGT | 317 |
rs141949581 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | APAF1 | GRCh38.p7 | 12:98708204 | CCCGCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 317 |
rs141959835 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | APAF1 | GRCh38.p7 | 12:98662145 | TTGGATAGTAATGGT[C/T]GCTTTTTTTTTTTTT | 317 |
rs141981472 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98703299 | GGACTTATATTTGAA[A/T]TGGGAGGATATTAGA | 317 |
rs142044358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98669395 | AAAAACAGAAAAAAA[A/C]GATGAAAAGGAAAAC | 317 |
rs142059001 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98683068 | GCATTTGCAAAGCAA[G/T]GGACATTGCTTTGCC | 317 |
rs142070777 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98711039 | CACCTCTGAATATGG[C/T]TTGCTTTGATTTTAC | 317 |
rs142112677 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | APAF1 | GRCh38.p7 | 12:98665186 | AGGCACACACCACCA[A/C]ACCTGGCTGATTTTT | 317 |
rs142160690 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98672257 | GCAACCTCTGCCTCC[C/T]GGATTCAAACGATTC | 317 |
rs142171589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98702420 | TTCTTTCTAAGGTCT[A/G]TGTCTTGATCTTAAA | 317 |
rs142230441 | snp | C/G | 1.66649e-05 | 0.00288655 | missense, utr-variant-3-prime, nc-transcript-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98732501 | ATACACGTGTCCCCT[C/G]ACTTCAAAACATATG | 317 |
rs142269091 | snp | A/G | 4.94409e-05 | 0.00497172 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723207 | GGTATGGAATTGGCA[A/G]TTGGACAAATGTATC | 317 |
rs142293344 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734407 | TTAAGGGCAATGGAG[A/G]TAAATTAATAGTAGA | 317 |
rs142318195 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | APAF1 | GRCh38.p7 | 12:98688297 | TCTTAAGATCAACCC[A/G]TCTTTGACATTGTTG | 317 |
rs142343936 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98690684 | CTGGGCCTTATTTGC[C/T]GCTGAATTATGGTCT | 317 |
rs142409655 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98728857 | AGTGATTGAGGCCGC[A/C]ATTTGAATGTGTTGT | 317 |
rs142416419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98652046 | TCTCGAACTCCTGAG[C/T]TCAAGCAATTCACCC | 317 |
rs142489760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98650224 | TTAGTAGGCCAGGCA[C/T]GGTGGCTCATGCTTG | 317 |
rs142510482 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98718434 | GAGACAAGGTTTCAC[A/G]ATGTTGGCCAGGCTG | 317 |
rs142533643 | snp | C/T | 0.000654189 | 0.0180739 | upstream-variant-2KB, synonymous-codon | APAF1, IKBIP | GRCh38.p7 | 12:98644645 | GCTCCGCTTCCCGGG[C/T]TCCGCAGCAGGGGCT | 317 |
rs142580021 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | APAF1 | GRCh38.p7 | 12:98653572 | TGAGGCATAAGAATC[A/G]CTTGAACATGGGAGG | 317 |
rs142752734 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | APAF1 | GRCh38.p7 | 12:98672457 | GGCATGAGCCACCAC[A/G]CCTGGCCTTCTGTGA | 317 |
rs142790780 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | APAF1 | GRCh38.p7 | 12:98656538 | AGTTGTTTGTTATAT[A/T]TTAGACTTTCATGCA | 317 |
rs142801463 | in-del | -/GTGA/GTGTGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98689495 | TGTGTGTGTGTGTGT[-/GTGA/GTGTGA]GAGAGAGAGACACAG | 317 |
rs142801831 | snp | A/C | 0.000626349 | 0.0176857 | intron-variant | APAF1 | GRCh38.p7 | 12:98677583 | GAGAAAAATGCAAAG[A/C]GGCATGTATCCAGTT | 317 |
rs142807564 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98718269 | AGACAGTCTTGCTCT[A/G]TTGCCTAGGCCGGAG | 317 |
rs142822252 | in-del | -/TA | 0.207559 | 0.246371 | intron-variant | APAF1 | GRCh38.p7 | 12:98667098 | TGGGGAGATTCTCTG[-/TA]TATATATATATGTAT | 317 |
rs142899470 | in-del | -/CCACAGCGCCTT | 0.292008 | 0.246445 | upstream-variant-2KB, utr-variant-5-prime | APAF1, IKBIP | GRCh38.p7 | 12:98644930 | GGCGGCGACCTCAAC[-/CCACAGCGCCTT]CCACAGCGCCTTCCA | 317 |
rs142906611 | snp | G/T | 0.000153988 | 0.00877328 | splice-acceptor-variant, intron-variant | APAF1 | GRCh38.p7 | 12:98706484 | TGTGTTTATTCTGTA[G/T]TTGTGGAATACAGAC | 317 |
rs142918745 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98651013 | TAAAATTGACTAACA[A/G]TCTATGGAATTAAAT | 317 |
rs142998333 | in-del | -/TTTA/TTTATTTA | 0.0011988 | 0.0244533 | intron-variant | APAF1 | GRCh38.p7 | 12:98672153 | TGTTTCCATGAAGAT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 317 |
rs143016650 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98649271 | ATAGATAGAAACTTC[C/T]ATTTTCTTTAGTCAT | 317 |
rs143020660 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | APAF1 | GRCh38.p7 | 12:98695089 | ATGGAGTCTTGCTCT[A/G]TTGCCCAGGCTGGAG | 317 |
rs143050298 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98712826 | ATACCTTTTTTTTTT[-/T]GAATCAGGATCTCAC | 317 |
rs143097832 | snp | G/T | 0.00115295 | 0.0239822 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699524 | GTGTTGTTCGTGGTC[G/T]GCTGATGGTGCAAGG | 317 |
rs143121294 | in-del | -/TGAGGTGA | | | intron-variant | APAF1 | GRCh38.p7 | 12:98697222 | TCTCAGGGAGTAGAG[-/TGAGGTGA]CTACCTCCTGTACAA | 317 |
rs143123251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98689562 | CTGGGCTAACTAAAG[C/T]GATCCTCCTGCCTCA | 317 |
rs143198215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98658134 | GATGCTACTGGAATG[A/G]TCTAATGCTACTGTT | 317 |
rs143208155 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98733579 | CTGAGACTACAGGCA[C/T]GAGCCACCACACCCA | 317 |
rs143246247 | snp | G/T | 0.00199806 | 0.0315443 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712339 | TAATGGAAGAACAGG[G/T]CAGATTGATTATCTG | 317 |
rs143274201 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98680975 | TATGAACTGGCTTAT[A/G]TATTCAGTGGAAAAC | 317 |
rs143434708 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98657496 | GACCTTGTGCAGGTT[C/G]AAAGACTCCATGTCA | 317 |
rs143451310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98670421 | CCTATTTTTTCTCTT[C/G]ACGTGTTTTTCTTTT | 317 |
rs143467699 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98699351 | TTTAGGAAAAATTCT[A/G]GAAGTGTGATTATAG | 317 |
rs143518770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98663841 | TTTTTGTATTTTCAG[A/T]AGAGACGGGGTTTCG | 317 |
rs143528358 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98715519 | AGCCGATGAGAAGAC[C/T]CTTATTTCAAGTTCT | 317 |
rs143555343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98664560 | TTTTTTTAAAGAGCC[A/G]GGGTCTTGCTCTGTC | 317 |
rs143578655 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98663331 | CAAAAAATAGAAACT[A/G]TTAGCTCTTTGTCAT | 317 |
rs143592994 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704678 | GCACACAGAGGCAGG[C/G]AGTGTGAAAAAGCTC | 317 |
rs143593431 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98659032 | CGTAAAATTTCTACT[C/T]TAAATCAAGAGAAGT | 317 |
rs143622471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98712759 | GTTTAAGCGATTGTC[C/T]GGCCTCAGCCTCCCA | 317 |
rs143683713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716299 | CCTGTCCTGCCTTCA[C/G]CTTATGTGCATGCAC | 317 |
rs143765428 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | APAF1 | GRCh38.p7 | 12:98717602 | GCTGGTCTTGAACTC[G/T]GGACCTCAGGTGATC | 317 |
rs143787749 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643656 | TTAGTTTTAAGTGAA[C/T]ACAAGTGCTATGTTT | 317 |
rs143842243 | snp | C/T | 0.000378803 | 0.0137571 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659206 | AGTTGGGAAACAAGA[C/T]AAATCTGGGCTTCTG | 317 |
rs143871220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98718849 | TGAGGTTGGAGGATC[A/G]CTTGAGCCTAGGAGG | 317 |
rs143938593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98647352 | AACTTCTAAACGTCT[A/G]TATATATTCATATGA | 317 |
rs143942135 | snp | G/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692744 | TCTTTTTTATGGCTG[G/T]GTTGTATCCCATGGT | 317 |
rs143961269 | snp | A/G | 3.30066e-05 | 0.00406229 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723668 | TACTGGAAATAAAGA[A/G]AAAGACTTTGTCTGT | 317 |
rs143963802 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667631 | ATCACATGGCCAGTG[C/T]CAAGATGCACAAGGT | 317 |
rs143982681 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646687 | TGAATTGATAAACCC[G/T]TTTAGACTCTTTCAC | 317 |
rs143985030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98695623 | TTTAGAAAAAAGACT[G/T]TCTCTTAATTTTCCT | 317 |
rs143989803 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98687028 | ACTGTAATTGCTTAT[C/T]GTAATGATTGTTTAT | 317 |
rs144097309 | snp | A/G | 0.00176413 | 0.0296471 | intron-variant | APAF1 | GRCh38.p7 | 12:98677406 | ATTTAATTTCTGTTC[A/G]TTTTTTCCCTGTATT | 317 |
rs144131396 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98699942 | CCTTTTTTTTCTTCA[A/G]TTTTGATTACATTGG | 317 |
rs144176447 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98709272 | CAATTGAAAGAACTG[C/T]ATTGCTTAGGGATCC | 317 |
rs144204135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98668384 | TGGATAGTGGAAAAG[C/T]ATATTCATTGATTCA | 317 |
rs144267380 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | APAF1 | GRCh38.p7 | 12:98669521 | CATAATAGAAATAGT[A/C]TCATATATTGCTTTT | 317 |
rs144336881 | snp | C/T | 0.000411912 | 0.0143453 | synonymous-codon, intron-variant | APAF1 | GRCh38.p7 | 12:98727190 | ATGGAATGTCTCAAA[C/T]GGTGAGCTTCTTCAT | 317 |
rs144360239 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | APAF1 | GRCh38.p7 | 12:98667196 | TAAACTCCTGGGCTC[A/G]GTTGGTCCTGAGTAG | 317 |
rs144417276 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98674332 | TGATTAAGACAAAAA[A/G]CAATAGTAATAGGAT | 317 |
rs144469589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646283 | AAATTAAGGAACATT[A/T]TATGTTTAAGAGGAC | 317 |
rs144474317 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | APAF1 | GRCh38.p7 | 12:98718280 | CTCTATTGCCTAGGC[C/T]GGAGTGCAGTGGTGC | 317 |
rs144579512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98712061 | GTCTCAGGTGGCGGG[C/T]GCAGCAGCTGCTTTT | 317 |
rs144595680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98693497 | TTTTTTTCCTCTCTC[A/G]TTAGCTTTCTGTTTT | 317 |
rs144643655 | snp | A/G | 3.31389e-05 | 0.00407042 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98665569 | CTCTCCCCTTGTAGT[A/G]TCTTTAATTGGTGCA | 317 |
rs144656472 | in-del | -/G | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | APAF1, IKBIP | GRCh38.p7 | 12:98643876 | CTGGAGTGCAGTGAT[-/G]GCGATCTTGGCTCAT | 317 |
rs144685671 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98652086 | TCCCAAAGTGCTGGA[A/G]TTGCAGGTGTAAGCC | 317 |
rs144715006 | snp | A/G | 9.89136e-05 | 0.00703186 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98677443 | CAAAAAAAACATCAC[A/G]AATCTTTCCCGCTTA | 317 |
rs144721573 | snp | A/G | 0.000610163 | 0.0174559 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666322 | CATGATCTTCAAGTA[A/G]ATTTTCTTACAGAGA | 317 |
rs144728788 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662710 | GTGGAGAGTTCCTTA[C/G]GAAAGGAAAAAGGAC | 317 |
rs144749677 | snp | A/C | 0.000710573 | 0.0188357 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98699566 | AGCAAAAAATAAAAT[A/C]TTTGTAAGTACTTTA | 317 |
rs144775569 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98660088 | CAGTGGCTCATGCCT[A/G]TAGTCCCAGCACTTT | 317 |
rs144787055 | snp | G/T | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649668 | AGAAGCTGTTAGAGA[G/T]CATTCCCTTTTAGAA | 317 |
rs144787965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98657342 | TCTTAGCACATACTC[C/T]TGACTCTTTAGTCCT | 317 |
rs144815185 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98650711 | GCCTGATTCCTAACC[A/C]TTGGTTTTTCCCCTC | 317 |
rs144824950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98731078 | CTTTTGGCCTTGAGA[C/T]AGGCTGCCTGAGTTC | 317 |
rs144825559 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98656206 | GTGCTGGGAGCCACC[A/G]TGCCAGGCTCTAAAT | 317 |
rs144848589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692481 | GCATGATGCTGATGC[C/T]GAGGTTTGGGTACAA | 317 |
rs144908006 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98674863 | AAATATTAGTTGTTA[C/T]TAAGAATAGCATTTA | 317 |
rs145015264 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | APAF1 | GRCh38.p7 | 12:98669386 | TTTCATTGGAAAAAC[A/G]GAAAAAAACGATGAA | 317 |
rs145031265 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98708103 | AGGTGCACACCACCA[C/T]GCCCAGCCAAGTTTT | 317 |
rs145098547 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98715350 | CTCCAGTCTAATTTT[A/G]GTTTAATATCTTTGG | 317 |
rs145099984 | snp | A/C/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730128 | AAAAAGAAAGGATGT[A/C/G]TGTTATCCCTTTACA | 317 |
rs145131107 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98710767 | AGCTCAGCTTGGTGT[A/G]GTGGAGAGAATAGTG | 317 |
rs145223718 | in-del | -/CCATG | | | intron-variant | APAF1 | GRCh38.p7 | 12:98692012 | CACTTAAGTAACATA[-/CCATG]CCTCAAAGTTATTGC | 317 |
rs145226502 | snp | A/G | 0.000297152 | 0.0121856 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648493 | AGGAAAAAGTAAGAA[A/G]TGAGGTAAAGCTCTC | 317 |
rs145244442 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98709072 | TTTAAAAGGGAAGGA[A/T]TCCAGGGTCTTTGAA | 317 |
rs145245931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719760 | TTGCTGTTATCTCCT[C/T]TCTCATTCTTTTGAT | 317 |
rs145257741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98659017 | TACCAGTATCTTGCA[C/T]GTAAAATTTCTACTC | 317 |
rs145263832 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734324 | AATAACTAGCTATTT[C/T]TGACCTCCTGATCAG | 317 |
rs145270473 | snp | C/T | 0.000378997 | 0.0137606 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98662526 | AGTCAGTGTCAGATT[C/T]TTCTTACAACCAGAG | 317 |
rs145299228 | snp | C/G/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | APAF1, ANKS1B | GRCh38.p7 | 12:98735800 | GGCCAGGGAGAGGCA[C/G/T]AAAAAGTAAATAAGT | 317 |
rs145339910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98729195 | TGAGTCTTTTGAATA[A/G]CAGTTTACTTGTAAA | 317 |
rs145363348 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98732326 | GCTTGAGTTCGGTTG[C/G]GGGGAGGAGATAGGG | 317 |
rs145393515 | snp | C/T | 0.000444726 | 0.0149052 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98667559 | AGAGATATCACCAGC[C/T]GCATACTCTTTCACC | 317 |
rs145403822 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98715158 | GAAGGACCACTGGTT[C/G]CTACTGCTGTCTGAT | 317 |
rs145414367 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | APAF1 | GRCh38.p7 | 12:98687865 | CGCCCAGGCTGGAGT[A/G]CAATGGTGTGATCTT | 317 |
rs145416277 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98734036 | TAATAAGATTTTTCT[A/G]AGAAATGTGAAATAG | 317 |
rs145431122 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98698000 | GGACCCTGGATACAG[A/T]GTAGCGACTTGCTCA | 317 |
rs145478792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98709422 | GAATGGTATTCAGGA[A/G]CTCGGAGTGGTGGTA | 317 |
rs145496423 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98694970 | AGATGGTGAACTTTT[A/G]ATGTCAAAGTCTTTA | 317 |
rs145497334 | snp | A/C | 3.30131e-05 | 0.00406269 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712408 | TCTTCAGTACATTGC[A/C]TTTGGAGATGAAAAT | 317 |
rs145559611 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98692942 | AATGGTAGTTCTGTT[A/T]TAAGTTATTTGAGAA | 317 |
rs145582430 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98705675 | CAGGATAAAATACCA[G/T]GCTGCTGGTAGACAT | 317 |
rs145624115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98694829 | AATGGGAATTGTGAA[C/T]TTTTAAATTGTGGTT | 317 |
rs145646542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98663943 | GATTATAGGCATGAG[C/T]TACCATACCTGGCCA | 317 |
rs145707116 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98711620 | TTTTAGTTTATGACA[C/T]TAAGAGAGAGGTATC | 317 |
rs145742976 | snp | C/T | 0.0410537 | 0.137264 | intron-variant, downstream-variant-500B | APAF1 | GRCh38.p7 | 12:98665349 | CTTAATAAAGATAAT[C/T]AGGAACTTACTGAAT | 317 |
rs145757678 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98684321 | GTATAAGAGTTAAAG[C/T]TTGCTGCTCTGGCTG | 317 |
rs145772658 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98680042 | AGAAAATCAACACCC[C/G]AAAGATCCTGTAACA | 317 |
rs145776709 | in-del | -/AGC | 0.00636936 | 0.0560724 | | | GRCh38.p7 | 12:98649876 | ATGAGATGACATCTT[-/AGC]AGGAGTTTGGAGAAA | 317 |
rs145807191 | snp | C/T | 0.00317431 | 0.0397124 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98706501 | TGTGGAATACAGACT[C/T]ACGTTCAAAGGTGGC | 317 |
rs145807330 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | APAF1 | GRCh38.p7 | 12:98661344 | TGTTGAGTAAAATAA[C/T]GTAGCCACTTTCAGA | 317 |
rs145836591 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98675964 | GAATAGATACCATTA[C/T]TTCCATTTGACATAT | 317 |
rs145961418 | snp | C/T | 0.021333 | 0.101051 | intron-variant | APAF1 | GRCh38.p7 | 12:98653638 | CTCCATCCTGGGTGA[C/T]AGAGTGAGATGCCGT | 317 |
rs146004775 | snp | A/C | 0.000153988 | 0.00877327 | upstream-variant-2KB, missense | APAF1, IKBIP | GRCh38.p7 | 12:98644698 | GGCTCTTCACCTCAG[A/C]CATGTCTGGAGACCC | 317 |
rs146017991 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | APAF1 | GRCh38.p7 | 12:98704712 | TCCTGTATGAAACAG[C/T]GGGAAGAAGTAGGGT | 317 |
rs146067706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | APAF1 | GRCh38.p7 | 12:98722124 | GCAGGTCCCTTTTCA[C/T]GTTTCCCTGCTCCTA | 317 |
rs146069069 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98701774 | TGCATGTAGATCCCG[A/C/T]TTTCTTACCCTTTGG | 317 |
rs146097285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98704361 | CAGATCACAGTTCCA[A/G]GAAGATGGGTATGGG | 317 |
rs146118725 | snp | A/G | | | intron-variant | APAF1 | GRCh38.p7 | 12:98708978 | TAAGAATACCATGAG[A/G]ACAAACTCATGTTGT | 317 |
rs146119246 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98682986 | AATATTGCCATATTT[-/T]AGAAAGGGGAGAGGT | 317 |
rs146140531 | snp | A/G | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98687260 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGAGAAT | 317 |
rs146191079 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98728005 | AAAATAAATAAAAAG[G/T]AAAAGAAAAAAAAAG | 317 |
rs146198251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98690288 | AGAGTTTAGCTAGCT[C/G]TTAGTGGGTGCTGGG | 317 |
rs146217019 | snp | C/T | 9.88843e-05 | 0.00703081 | intron-variant | APAF1 | GRCh38.p7 | 12:98686883 | TTAAAGGTATGCTTT[C/T]GTACACTATTAAAAT | 317 |
rs146238655 | snp | A/G | 0.0020579 | 0.0320112 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98723220 | CAATTGGACAAATGT[A/G]TCTTTCTACGAGGCC | 317 |
rs146297180 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98667887 | GTGATCCTCCCACTT[C/T]AGCCCCCCATGTAGC | 317 |
rs146300180 | in-del | -/TAGTTAC | 0.00914312 | 0.0669923 | intron-variant | APAF1 | GRCh38.p7 | 12:98711395 | GAATAAAACATTTTT[-/TAGTTAC]TACTTAAAGAATTCT | 317 |
rs146317828 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | APAF1 | GRCh38.p7 | 12:98672275 | ATTCAAACGATTCTC[C/T]TGCCTCAGCCTCCAA | 317 |
rs146324917 | snp | A/C/G | 6.65064e-05 | 0.00576623 | intron-variant, synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98648811 | TAGTGGAATAACTTC[A/C/G]TATGGTTTGTATCCA | 317 |
rs146382169 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98688839 | CTTTTTTTTGAAACA[A/G]GGTCTTATTCTGTTG | 317 |
rs146390216 | snp | A/G | 0.00214041 | 0.0326439 | intron-variant | APAF1 | GRCh38.p7 | 12:98723777 | AAGGTAGGTCAATCA[A/G]TTGAAACCATGCATA | 317 |
rs146420669 | snp | A/G/T | 0.000544252 | 0.0164888 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98708697 | TTGACCATATAAGAC[A/G/T]TCTGCAAGTGAGTAT | 317 |
rs146424586 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98671040 | TTGTAGGCCCTGCTC[A/G]TCTGATTCATGAATT | 317 |
rs146437624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646755 | ACTTGCAGATATTGT[A/G]AACTGGGTTTTATGC | 317 |
rs146505676 | snp | A/G | 0.0009057 | 0.021261 | synonymous-codon, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98659284 | TTCCCAGAGGCTTCC[A/G]CTTAATATTGAAGAG | 317 |
rs146524415 | snp | A/G | 0.198944 | 0.244731 | intron-variant | APAF1 | GRCh38.p7 | 12:98702191 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 317 |
rs146613849 | in-del | -/GTTA | 0.0547245 | 0.156101 | intron-variant | APAF1 | GRCh38.p7 | 12:98723493 | ATGAGCATTTATACT[-/GTTA]GTCACATTTAAAGTA | 317 |
rs146615927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98680094 | ATGTAACAGTGAATA[A/G]TTCTCTAGTTATGTG | 317 |
rs146641691 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | APAF1 | GRCh38.p7 | 12:98684008 | TGGAATCCCAGAAAG[A/G]TCTGCTAACTTTTTT | 317 |
rs146673680 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98683348 | CTTTGATTTTCTTAT[G/T]TATACTACTATTAGG | 317 |
rs146734785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98660705 | GGTTCTGGGCCAAGT[A/G]CTGCAAGTACAAAGA | 317 |
rs146801709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98663560 | GTTGTATTCTTTTGA[C/T]ATATAGAAGCTTAAA | 317 |
rs146874832 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | APAF1 | GRCh38.p7 | 12:98679768 | TCCAGCCACAGCCTC[A/G]CAGAGAGCCAGAGCC | 317 |
rs146885431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98675293 | TTTGGGCCATCTACT[A/C]TATATCCTTTATTAT | 317 |
rs147031167 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98685081 | AAGTGGACATGAGGA[A/G]CAGTATATATCTCAC | 317 |
rs147047265 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98681421 | TTTGGCTTCTACCAG[A/G]AGCATTTATACTAAT | 317 |
rs147107691 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | APAF1 | GRCh38.p7 | 12:98665874 | TGTTGTTACAGAGAA[C/T]CTTGGAAGGATAAGA | 317 |
rs147199448 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98713041 | CCAGGCTGGCCTTAA[A/T]CTCTTGGGCTCAAGT | 317 |
rs147222625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98718063 | AACATTTAGTATGTA[C/T]ACCTTCCCTTGATCC | 317 |
rs147249307 | snp | A/G | 0.000329489 | 0.0128311 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98666243 | TGAAGACATACTGCA[A/G]GAGTTTGTAAATAAG | 317 |
rs147264833 | in-del | -/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98719516 | ACCATTTCCGGCTAA[-/T]ATTTTTTTTTTTTTT | 317 |
rs147306238 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | APAF1 | GRCh38.p7 | 12:98695707 | CTGCCAGAGTAGGGA[C/T]ACAGGCCCCCTGGGT | 317 |
rs147312968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98657790 | TAACTTTGGGCAAAT[C/T]ACTCAACTTTTCTAT | 317 |
rs147330076 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | APAF1 | GRCh38.p7 | 12:98655984 | GAAACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 317 |
rs147400886 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | APAF1 | GRCh38.p7 | 12:98682299 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 317 |
rs147417898 | snp | A/C/G | 0.00593574 | 0.0541538 | intron-variant | APAF1 | GRCh38.p7 | 12:98677589 | AATGCAAAGAGGCAT[A/C/G]TATCCAGTTTTGTGC | 317 |
rs147505651 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | APAF1 | GRCh38.p7 | 12:98662096 | TTCTAGTTTGGTTTT[A/G]GTGCTTAAAGACTGA | 317 |
rs147522046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98658295 | ATGTTTTATGGCTCA[A/G]TTAACAATGATGATG | 317 |
rs147585547 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | APAF1 | GRCh38.p7 | 12:98709090 | CAGGGTCTTTGAAAG[A/C]ACAGAAGTCACTTTA | 317 |
rs147589428 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | APAF1 | GRCh38.p7 | 12:98705957 | TATCCCTTCGCCTCG[C/T]TCTCCCTCCTTCCCT | 317 |
rs147683192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98692997 | ACCGAACAAATTTAC[A/G]TTCCCACCAGCAGTG | 317 |
rs147699305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98688154 | CAGCCTTCTGAAATT[C/T]ATAGGCCTAAAAAAA | 317 |
rs147700706 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649541 | CAGTTGTTTTTGTCA[C/T]AAGGAAGAAGCTGGT | 317 |
rs147804308 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98669966 | CAGGATCTCACCAGG[A/T]TGTCACTCTGTTGCC | 317 |
rs147850238 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98726481 | GTGCAGAAGACTAGG[A/C]GAGTATACAGTTTGC | 317 |
rs147892161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98656331 | AACACAGCTTTAAGT[C/T]TAAGTGAAGTCTCAA | 317 |
rs147901080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728925 | TATCTTTTATCTATC[C/T]ACTCAAAAAGACTGT | 317 |
rs147904570 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | APAF1 | GRCh38.p7 | 12:98725958 | AGATCTCTTTAGCAC[G/T]ATACCCATTTGATAG | 317 |
rs147908953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98652153 | AGACAGGTTTTTGCT[A/G]TCTTGTCCAGGCTGG | 317 |
rs147932236 | snp | C/T | 0.000569845 | 0.01687 | missense, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98649673 | CTGTTAGAGATCATT[C/T]CCTTTTAGAAGGTAA | 317 |
rs147971793 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98657505 | CAGGTTCAAAGACTC[C/T]ATGTCACTTCAAGTT | 317 |
rs147973432 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | APAF1, ANKS1B | GRCh38.p7 | 12:98732772 | GTTTTTCATGATCAT[C/T]ATTAACAGTTTGTCC | 317 |
rs148108264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98704117 | TTTCCTTCAAAGATG[A/G]ATTAGTGCTTTTTTT | 317 |
rs148115333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98716390 | ATCCTTCCTGTTACT[A/G]TGATCACTGTGTACT | 317 |
rs148165039 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98670912 | GTGAGGTTAATGATG[G/T]TATACCTAAAATTTT | 317 |
rs148185299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98695114 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACC | 317 |
rs148237361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98689905 | TGTTCAGTCATTTTA[A/C]TGTGTCTTCTGTTTC | 317 |
rs148273308 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98649756 | TATGATATATCAATA[C/T]GTGATAAATTGAATG | 317 |
rs148324424 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | APAF1 | GRCh38.p7 | 12:98667368 | TGATCCTCCTACCTT[C/G]GCCTCCCAAAGTGCT | 317 |
rs148325167 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | APAF1 | GRCh38.p7 | 12:98681130 | GCAGTGGTACAATCT[C/T]GGCTCACTGCAATCT | 317 |
rs148431164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | APAF1, IKBIP | GRCh38.p7 | 12:98646593 | GTAGACTGTGAATTA[C/T]TTCAGGCAAATGACT | 317 |
rs148475519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98672880 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC | 317 |
rs148491682 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98712146 | GGATTGAAATGAAAG[A/C/T]GTGAAGTGCTAAATG | 317 |
rs148495006 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | APAF1 | GRCh38.p7 | 12:98696926 | CTGTTCTGAACTGTT[A/C]AGAATAAAGTTGGAG | 317 |
rs148551763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98662107 | TTTTGGTGCTTAAAG[A/C]CTGAGTTGGAAAATC | 317 |
rs148588457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | APAF1 | GRCh38.p7 | 12:98650874 | GAAGGAATGAGTTTT[C/T]CTTTCAATATTATGA | 317 |
rs148685304 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | APAF1 | GRCh38.p7 | 12:98708237 | GGTGTGAGCCCCTGC[A/G]CCTGGCCCAAACTTC | 317 |
rs148710599 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | APAF1 | GRCh38.p7 | 12:98659023 | TATCTTGCACGTAAA[A/G]TTTCTACTCTAAATC | 317 |
rs148758248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98728647 | ACTCACTTGAACCCC[A/G]GGGGAGCAGAAGTTG | 317 |
rs148808800 | snp | A/G | 0.207253 | 0.246318 | intron-variant | APAF1 | GRCh38.p7 | 12:98687297 | AACCCGGGAGGTGGA[A/G]GTTGCAGTGAGCTGA | 317 |
rs148854272 | snp | C/T | 0.0011566 | 0.0240201 | synonymous-codon, intron-variant, nc-transcript-variant | APAF1 | GRCh38.p7 | 12:98712429 | AGATGAAAATGGAGC[C/T]ATTGAGGTATTCAGT | 317 |
rs148864265 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | APAF1 | GRCh38.p7 | 12:98663950 | GGCATGAGCTACCAT[A/G]CCTGGCCACCTTATT | 317 |
rs148910969 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | APAF1 | GRCh38.p7 | 12:98726723 | CACTGCAGGAAAAAG[A/T]TGTCTCCATTAAAAT | 317 |
rs148968107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98684741 | AAATGTACCACTAAA[A/G]AAAAATAAGACTGTT | 317 |
rs148969717 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | APAF1 | GRCh38.p7 | 12:98682581 | ACTATAAAACCTTTA[-/T]TTTTTTTAACTAAGC | 317 |
rs149073415 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | APAF1 | GRCh38.p7 | 12:98702236 | GCGCCCGGCTAATTT[C/T]TTGTATTTTTAGTGG | 317 |
rs149082685 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | APAF1, ANKS1B | GRCh38.p7 | 12:98730658 | GCTTATTCAACTGAT[A/T]ATGATATAGCCCAGC | 317 |
rs149172292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | APAF1 | GRCh38.p7 | 12:98719763 | CTGTTATCTCCTTTC[C/T]CATTCTTTTGATCTT | 317 |
rs149194964 | snp | C/T | | | intron-variant | APAF1 | GRCh38.p7 | 12:98680927 | GTTGTAAGATACAAT[C/T]TTAAAATGCAACCCC | 317 |