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 |