SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3057 | snp | A/G | 0.460813 | 0.134379 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317591 | CTGATGGAAGCATCA[A/G]TGATGGATTTGGCTT | 50807 |
rs716077 | snp | A/G | 0.328616 | 0.237317 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113467 | TCATTATAAGAGTAT[A/G]GAAAAATTCCTGAGA | 50807 |
rs749126 | snp | A/G | 0.233527 | 0.249457 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091180 | GTTTACTGGAACCAC[A/G]CCTGGCATACAGTGA | 50807 |
rs752716 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079169 | cactgcactccagtc[C/T]gggtgacagagaaag | 50807 |
rs754021 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289527 | TCTTAAAGTTTGGAC[C/T]AGTCTGCAAGGTAGC | 50807 |
rs876575 | snp | A/G | 0.474 | 0.111014 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198605 | GGTACTGTATCTAAC[A/G]TATATTATCTAAAGA | 50807 |
rs897050 | snp | A/G | 0.321053 | 0.23969 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106826 | AGTATTCCTGGAGGA[A/G]CAGGAAAGAGAAGTG | 50807 |
rs897052 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055461 | GGCAAGACCCACTGC[A/G]GGGTACCATACTCAA | 50807 |
rs897053 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055739 | AGAGAATCATGTAAT[A/G]GGCCTTCAATAGAAA | 50807 |
rs929990 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264814 | AACACACGATGATCA[C/T]TATGTACGCAAAGGG | 50807 |
rs966185 | snp | A/G | 0.498842 | 0.0240367 | missense | ASAP1 | GRCh38.p7 | 8:130112313 | TGCCAGCCAAGCCCT[A/G]TCAAGAAAGAGCGCT | 50807 |
rs1008819 | snp | C/T | 0.360842 | 0.224085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263914 | TGTCATTATTGTCTA[C/T]GTTACTTTAGACACA | 50807 |
rs1017281 | snp | C/T | 0.489608 | 0.0713316 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234967 | ccacatagtaggtgc[C/T]taacaaatggtagAT | 50807 |
rs1030386 | snp | C/T | 0.161267 | 0.233723 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311270 | TTTTCAAGTTTTCCC[C/T]AATGGCCATATTTTA | 50807 |
rs1031473 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067730 | AGAATACAGGAAAAC[A/G]CTGGGTTCTTAATGG | 50807 |
rs1031474 | snp | A/G | 0.39527 | 0.203462 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105751 | CACTAGTGTCCCAGC[A/G]CACTCTACTCCACCA | 50807 |
rs1031475 | snp | A/T | 0.397452 | 0.201886 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105666 | TCCTTCTTTGTATAA[A/T]TATACGGTTAATTAC | 50807 |
rs1118887 | snp | A/T | 0.473266 | 0.112482 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189775 | ggaactctcatacgc[A/T]gttggtggtaatata | 50807 |
rs1123205 | snp | C/G | 0.486855 | 0.0799975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336864 | GAGAAGTAGTTTCTT[C/G]AAATGTTCTCTGGTG | 50807 |
rs1158569 | snp | A/C | 0.496746 | 0.040204 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318766 | TAACTTCAAATATAG[A/C]CTAGACACTTAAAAA | 50807 |
rs1158570 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318827 | TTGTCAGTGGAAATG[C/T]CAAATGGAGTGGCCA | 50807 |
rs1298714 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276728 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 50807 |
rs1340019 | snp | C/T | 0.248188 | 0.249993 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343801 | TGTCATTGTATTAAA[C/T]GTTTCCCTCCCTCCC | 50807 |
rs1340020 | snp | A/C | 0.357664 | 0.225629 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343755 | TTGTGTGTTTTGTAC[A/C]GTTGGCTTAGCAGTT | 50807 |
rs1340021 | snp | C/G | 0.49306 | 0.0584955 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337072 | GTGAGTCCTGACTGG[C/G]TTAGCTATTTGTGAT | 50807 |
rs1340022 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322219 | TCAGTTTCTTATGCA[A/G]TTTTTCACTGCATAC | 50807 |
rs1365181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217861 | CTGGGTTATTTCCCA[A/G]TCCAGACTCATGTTC | 50807 |
rs1365182 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235257 | CTGAAGCCTTGATTG[C/T]GATTTGGAAGAGCAG | 50807 |
rs1417007 | snp | C/G | 0.333952 | 0.235483 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340340 | TAACCTTGTTTGACT[C/G]TTTTGTAGGCTAAAT | 50807 |
rs1417008 | snp | G/T | 0.226188 | 0.248863 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265006 | GACTAAAATTACTGG[G/T]GTACAAGGAAGTGGT | 50807 |
rs1417009 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265080 | AGGATGTGGCCCTTT[A/T]CTCATGGCAACAAAG | 50807 |
rs1417010 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268818 | CATTTGCAGTCTCCA[C/T]AAAATTATACTACTG | 50807 |
rs1426101 | snp | A/G | 0.388701 | 0.211287 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230514 | AGGGTCAAGGAAGGG[A/G]TTTTTTTCCCCCAAA | 50807 |
rs1426102 | snp | C/G | 0.24019 | 0.249807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301123 | CCCAGCATAAGCAGA[C/G]GACATGAGAAATAGT | 50807 |
rs1469285 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217587 | AGGTAATCCCTGCCT[C/T]TTGCGGTCTGGTGGT | 50807 |
rs1469286 | snp | C/T | 0.33533 | 0.234987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214773 | AGAATTCGTAGTGAT[C/T]GGTGTTCAAAGTAAC | 50807 |
rs1469287 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214503 | CTTTCCAAAATATTA[C/T]GTCATATAGAGAACA | 50807 |
rs1469288 | snp | C/T | 0.474363 | 0.110278 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214406 | AGTCCTAGGTAACTT[C/T]CACACCTCAACTAAA | 50807 |
rs1538728 | snp | C/T | 0.497695 | 0.0338674 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336114 | CTGTTTCTGAAACTT[C/T]GTTTTGCATTATCTT | 50807 |
rs1549454 | snp | A/G | 0.357238 | 0.225832 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249740 | TACAACTGGGAGGAA[A/G]TAATATATAAATAAA | 50807 |
rs1549455 | snp | C/T | 0.341685 | 0.232581 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252774 | GGAAAATAATAATTA[C/T]AGGTACAACAAGGTA | 50807 |
rs1556972 | snp | C/G | 0.233527 | 0.249457 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263324 | GTCAGATCCCACCCT[C/G]TCAGGAATTTGAACT | 50807 |
rs1801625 | snp | A/C | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052884 | AGCCACACCAGTGTC[A/C]GGATGGAAGTCTGCA | 50807 |
rs1815642 | snp | A/T | 0.0182089 | 0.0937193 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288784 | CAGCAGCATTACTTA[A/T]AGAAGAAAAGAAGGG | 50807 |
rs1934563 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298655 | TAATGGGGAACAAGA[A/C]CGGTAATGAGCCTGG | 50807 |
rs1960661 | snp | C/T | 0.328616 | 0.237317 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189995 | CATAGGAAAAAAATC[C/T]AGTTTTAAACTGGGC | 50807 |
rs1974313 | snp | A/G | 0.336474 | 0.234568 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263069 | TTTTTACTAATACGA[A/G]TATGAATTTACTAAT | 50807 |
rs1978550 | snp | C/T | 0.499121 | 0.020948 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263786 | AATAACAACTTCCAG[C/T]GCCTTCTACCAACTA | 50807 |
rs1978551 | snp | C/G | 0.350546 | 0.22889 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245549 | GGTGGTGTTTTCTTG[C/G]ATGGACTAAATCCTT | 50807 |
rs2005040 | snp | G/T | 0.475081 | 0.108804 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289211 | AAGTATAGTTTTTTT[G/T]TTTGTTTGTTTTTGT | 50807 |
rs2009449 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296884 | CCTCTCCCTGGCCAG[G/T]GGTTCTTATTTACTT | 50807 |
rs2027377 | snp | A/T | 0.342582 | 0.232225 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309403 | TTAGTCTAAGTGTCA[A/T]AGCACCCAAAGTCTT | 50807 |
rs2033059 | snp | C/T | 0.457154 | 0.139954 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258970 | CCCTATTTGCCCCAT[C/T]GATTCCAAAAATAAA | 50807 |
rs2045091 | snp | A/G | 0.318896 | 0.240319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063613 | GGAAGATGAAGCTAC[A/G]TCATGCAGCAGGTCT | 50807 |
rs2045092 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063400 | TGTGGACAGGGTCTA[A/G]ATACCTGAAGCTGGG | 50807 |
rs2045093 | snp | C/T | 0.354665 | 0.227036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079346 | AAGGCTGGATAAAAA[C/T]TGCCCGTAAGAGATC | 50807 |
rs2052710 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254841 | TTTCTTAAGTAGCAA[A/C]AACCAATCTAACAAC | 50807 |
rs2085064 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090508 | AATGAATTAGTTCCC[A/C]CAAGCCAGGCAAGAA | 50807 |
rs2114196 | snp | C/T | 0.470034 | 0.11868 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213053 | CACTTTCACTGGAGG[C/T]CTTGCTCAAAGTGTG | 50807 |
rs2114197 | snp | A/G | 0.175254 | 0.238565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244811 | TCCAGGATTGCAGGG[A/G]TTAAAGATGGAGATG | 50807 |
rs2123870 | snp | G/T | 0.476746 | 0.10529 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064174 | aacctggtcctgcag[G/T]ctgttctcaacagaa | 50807 |
rs2185366 | snp | A/G | 0.468949 | 0.12067 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330476 | GGTGTTCACAGGTGA[A/G]TGGGGTGGTGGTTGT | 50807 |
rs2303444 | snp | C/T | 0.219435 | 0.248125 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214506 | AGCCTTTCCAAAATA[C/T]TACGTCATATAGAGA | 50807 |
rs2305510 | snp | A/C | 0.223789 | 0.248622 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126098 | GTGGGTTCTGTGGAA[A/C]GAATGTTGAAGACAA | 50807 |
rs2305511 | snp | A/C | 0.357238 | 0.225832 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126329 | AGAAAGGCTTTCCTT[A/C]AGAGACCCTATGCAA | 50807 |
rs2305512 | snp | C/T | 0.00113632 | 0.023809 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130115694 | CAATCCACACGTCCA[C/T]GTAGAATATGAGTGG | 50807 |
rs2305513 | snp | A/G | 0.495821 | 0.0455185 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115585 | TCAACAACTACCCCA[A/G]CTTTTCTAGTCTGTG | 50807 |
rs2395989 | snp | C/T | 0.321769 | 0.239477 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068628 | ctgcatatgggtata[C/T]atgatccagacacac | 50807 |
rs2395992 | snp | A/G | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230846 | ATTCTAATCTATTAT[A/G]TCTCTTACATATGCT | 50807 |
rs2396015 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197455 | Gttcttttcttttct[C/T]ttttcttttgagaca | 50807 |
rs2554367 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 8:130262482 | ATTTCAAATAGGTTA[A/G]ACAGAAGGTTTATTC | 50807 |
rs2554368 | snp | A/G | | | | | GRCh38.p7 | 8:130267786 | ATATTTTCTCCTTGA[A/G]AAAATCTTCCCGTAA | 50807 |
rs2554369 | snp | A/G | 0.39527 | 0.203462 | | | GRCh38.p7 | 8:130301801 | CAGATATGCATATGC[A/G]TTGTTGTTGAGAGTA | 50807 |
rs2554370 | snp | A/G | | | | | GRCh38.p7 | 8:130249493 | TAAGAAGATGATGGA[A/G]AAAATGGTGAGAGGC | 50807 |
rs2554371 | snp | A/G | | | | | GRCh38.p7 | 8:130249202 | GACTAGACATATTTA[A/G]AAACACTCTGCAATG | 50807 |
rs2554372 | snp | A/G | 0.469544 | 0.119585 | | | GRCh38.p7 | 8:130321667 | TCATTTTATATTTAA[A/G]CAACCATGGAAATAC | 50807 |
rs2554373 | snp | A/G | 0.486 | 0.0824865 | | | GRCh38.p7 | 8:130246289 | CCATTGGTACAAAAG[A/G]CAGAGTGGTTTAATG | 50807 |
rs2554374 | snp | A/G | 0.498908 | 0.0233371 | | | GRCh38.p7 | 8:130244152 | AATAGGTCTGATACC[A/G]TGCTACCTGTTGGGG | 50807 |
rs2554375 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 8:130284104 | GGGTTTTGTCCATTA[A/G]AACCTCTGTCCTCCG | 50807 |
rs2670873 | snp | C/T | 0.46885 | 0.12085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316056 | AGAGAAAAGCACTTC[C/T]GTCTTTTCAGCTTAA | 50807 |
rs2670874 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317322 | TGATATTCCTCCCTT[C/T]TCAGCCAAAATTGGG | 50807 |
rs2670875 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262623 | GGAAAGTAAGGGGTT[C/T]TTTTAGTCTAAATAT | 50807 |
rs2670876 | snp | A/G | 0.228842 | 0.249103 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257640 | CCAAATTTACCGACT[A/G]TAGATCCCTTTTTTT | 50807 |
rs2670877 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335769 | ATAGTCTGAGGTTAA[A/G]AAAATGTAGCTCAGG | 50807 |
rs2670878 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130335786 | AAATGTAGCTCAGGA[A/G]AAAATCCTGTGAACA | 50807 |
rs2670879 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330511 | taacagaatgaatta[A/G]acatgctttctgtcc | 50807 |
rs2670880 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329222 | TGGAAAACTTATTTA[G/T]TTAAGTGGCTTAGTG | 50807 |
rs2670881 | snp | G/T | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327308 | AGCTTGCCCAACAAT[G/T]TTGGTACAACAGTTT | 50807 |
rs2670882 | snp | A/G | 0.165527 | 0.235296 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325590 | CTTTCCTCTTTGTAT[A/G]TCCCAAAACGCCTTC | 50807 |
rs2670883 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324394 | AGTTGGTTAATGATA[C/T]TCAACCTTTTCATCC | 50807 |
rs2670884 | snp | A/G | 0.494143 | 0.0537956 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243588 | TGGCTGGAACATAAT[A/G]AGTAGTGGAGGGTGT | 50807 |
rs2670885 | snp | A/G | 0.403684 | 0.197183 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275862 | AACTACATTCCTCAC[A/G]GAGAACAACAGAACT | 50807 |
rs2670886 | snp | C/T | 0.163892 | 0.234703 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244432 | AATCCAAAATGACCA[C/T]GTGGGTACAATAAAC | 50807 |
rs2670887 | snp | C/T | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245956 | CGGGACTCTTGGAGG[C/T]TACAGTGGTTCCCAA | 50807 |
rs2670888 | snp | C/T | 0.38934 | 0.207568 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247918 | GCATGTGTACCTGCA[C/T]ACAGAAAATAGGCTT | 50807 |
rs2670889 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303049 | TTCCCTTCTGCCTTA[A/G]GTATGGATTCTTTGG | 50807 |
rs2670890 | snp | C/T | 0.387263 | 0.208947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302677 | CTTGAGATGTCCCCA[C/T]GTGCCCCTCCCCCTC | 50807 |
rs2670891 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268457 | CATGCCATTATACTC[C/T]AGCCTGGGTGACAGA | 50807 |
rs2791338 | snp | A/G | 0.388587 | 0.208071 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273391 | CTGCTTCCACTCAAG[A/G]TCTGCAGAAGGGGAA | 50807 |
rs2791339 | snp | C/T | 0.135825 | 0.222405 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275688 | GAAACGTAAGCATTT[C/T]GATGCTTTTAAAATT | 50807 |
rs2791341 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297978 | TGGGAGCTGAAACAT[C/T]TGGGTTCCAGTCCCA | 50807 |
rs2791342 | snp | C/T | 0.420255 | 0.183066 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302183 | TTGAAAAACCATGTA[C/T]AACTTTTCACCTTAA | 50807 |
rs2791343 | snp | C/T | 0.451359 | 0.148171 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303784 | tgagggaaggagaga[C/T]gactaggtggaccac | 50807 |
rs2791344 | snp | C/T | 0.467845 | 0.122652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310246 | AATAATAGAAATAAC[C/T]ATTGTTATGGGCTCA | 50807 |
rs2791345 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319861 | TGACAAAAAAACTTT[C/T]TAGGTGAAAAAGGCA | 50807 |
rs2791346 | snp | A/T | 0.247053 | 0.249983 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320686 | TGTAGCTTTCCACAC[A/T]ACCAGGAAGAAGTAT | 50807 |
rs2791347 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130327135 | GGGCACTTTATCTTT[C/T]TGAGCAGATGTAATG | 50807 |
rs2791348 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329262 | CCATCCTGGTCTCTG[G/T]TGCTCCTCTCAAAAC | 50807 |
rs2791349 | snp | A/C | 0.360632 | 0.224189 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333660 | TGTAACAATTTTTTT[A/C]AAGTATGGCAGGGCA | 50807 |
rs2791350 | snp | C/T | 0.420574 | 0.182769 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339107 | TAAATACAGATACAG[C/T]GACTCTTCATTGGAG | 50807 |
rs2791351 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342310 | ccttccctcagtttt[C/T]tcatctgtaaaatga | 50807 |
rs2791352 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346459 | ATCTGCATTTTTTTT[C/T]TTGAGGATGAGTCTG | 50807 |
rs2791353 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262416 | aaaaaaaaaaaaaaa[A/G]agagagagagagaga | 50807 |
rs2791354 | snp | A/G | 0.225005 | 0.248747 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350995 | TCTGCCCAGTCCAAG[A/G]AGGATTGCTTGCAGC | 50807 |
rs2894508 | snp | A/G | 0.497151 | 0.037632 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233341 | CTCAACAAGGGTTGA[A/G]TGAATCGCTACATGT | 50807 |
rs2912191 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287790 | CTTTAACATAGGGAA[C/T]GCTCAGAGGGCTGTG | 50807 |
rs2912192 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300155 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 50807 |
rs2912193 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247605 | TTTTACATAGAGCCT[C/G]CTGGAATGGGAAGAA | 50807 |
rs2912194 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285943 | AAGTTAAGACAGGTA[C/G]CAAATTATTTATGAT | 50807 |
rs2943086 | snp | A/G | 0.387642 | 0.208697 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318732 | ACGTGATAGAGTTGG[A/G]GTTCAGTCCATGTTC | 50807 |
rs2994295 | snp | G/T | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283979 | CTAAGAGTGGGTATT[G/T]CACTGACTGTATCCA | 50807 |
rs2994296 | snp | C/T | 0.136847 | 0.222927 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286117 | TTATTTGCTATTTTC[C/T]AAATGAAGAAAAGAA | 50807 |
rs2994298 | snp | A/G | 0.242775 | 0.249896 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330627 | GAGGCCTTCATGAGC[A/G]TTTAAGGTTTATATT | 50807 |
rs3078915 | in-del | -/CAGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074487 | acacacacacacaca[-/CAGA]GAGAGAACGAGAGTA | 50807 |
rs3078919 | snp | C/T | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080478 | TCATTCATTCTCTCT[C/T]TTTTTTTTTTTTTTT | 50807 |
rs3079890 | in-del | -/CT | 0.493969 | 0.05458 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336059 | CTACTCAACTCCAAA[-/CT]CTGTCTCATCAGCCT | 50807 |
rs3079892 | in-del | -/ACG | 0.45889 | 0.13735 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342754 | TGCCAACTCTCAGAA[-/ACG]ACAAGTTAAAGTTGC | 50807 |
rs3106532 | snp | G/T | 0.0637235 | 0.166737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246894 | CTGTGGGTACTCATA[G/T]TAACTTAGTGCCAGA | 50807 |
rs3217641 | in-del | -/T | 0.319381 | 0.24018 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115778 | AATATTGGGATGTTT[-/T]CAGCATTTAAATTAA | 50807 |
rs3758027 | snp | A/C | 0.000955204 | 0.0218332 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054712 | AAGGATGTGGACAAT[A/C]TTAAGGTTCTGCGTT | 50807 |
rs3758028 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055871 | GGCTTGCCCACCCAC[C/T]GCGTGTGGTCTTAGT | 50807 |
rs3812476 | snp | A/G | 0.330714 | 0.236612 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110398 | GCCTCCAGACTGAAT[A/G]CAATAATGGAAAAAG | 50807 |
rs3891541 | snp | C/T | 0.273856 | 0.248859 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312462 | GGAGGGGAAAAAAAA[C/T]CCATTAGGAATTCTG | 50807 |
rs3924350 | snp | A/G | 0.273049 | 0.248935 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372608 | AGAATTCAAGCCACA[A/G]TGACATAAGTGAGGA | 50807 |
rs3924416 | snp | A/C | 0.248188 | 0.249993 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375002 | TCCAGTTAGGCTAAG[A/C]TCCCAAAGCTGACTT | 50807 |
rs3924865 | snp | A/T | 0.487746 | 0.0773096 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417477 | CTTTCCGCCCGTATC[A/T]CTTGTGTCAGAGCGA | 50807 |
rs3935174 | snp | A/T | 0.470565 | 0.117691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152840 | CCCAGAGTGAATCAG[A/T]TACTATATCTAGTTG | 50807 |
rs3937694 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090238 | GAAGTGCCTTTATTC[A/C]CATTGTATAGACTCG | 50807 |
rs3997633 | in-del | -/AACAAACA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230099 | ACAAACAAACAAACA[-/AACAAACA]CCAACCCCAAACTAG | 50807 |
rs4130059 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363463 | TAAGTATAGAATTTA[A/G]AATACATTTATCCTT | 50807 |
rs4236749 | snp | C/T | 0.336474 | 0.234568 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052907 | GTGTGGCTTCAGTAC[C/T]GAGGCTGCTAAAGCT | 50807 |
rs4259451 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190189 | tttttgctttggttg[A/T]ctgtgcttttgaggt | 50807 |
rs4281151 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107438 | gatccgcccgcctca[A/G]cctcccaaagtgctg | 50807 |
rs4319146 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107564 | tgtatgtatgtattt[C/T]tgagatagagtctca | 50807 |
rs4363239 | snp | A/C | 0.25634 | 0.24992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352827 | GAATCTACATTCTGT[A/C]TCTTCATTCATTTCA | 50807 |
rs4504679 | snp | A/G | 0.458545 | 0.137872 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408742 | attcagacaatcaca[A/G]ttccttgcaaagttc | 50807 |
rs4526396 | snp | C/T | 0.424659 | 0.17887 | intron-variant | ASAP1 | GRCh38.p7 | 8:130388902 | ggctccagggccaga[C/T]tccctgcagccaagt | 50807 |
rs4574884 | snp | A/G | 0.413914 | 0.188765 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355235 | CACAGAGATTTAACT[A/G]AAAGCATCAACATCT | 50807 |
rs4609234 | snp | A/G | 0.457154 | 0.139954 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397639 | GTGCCAGTTAAGCAA[A/G]GGATGGGGGGAACTG | 50807 |
rs4629915 | snp | C/T | 0.246769 | 0.249979 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130386823 | CCACTTTTAGGTTCA[C/T]GGCTCAGCCAAAAAC | 50807 |
rs4639572 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106412 | TGGCAGGTGCTGTCA[C/T]ATACTGAGCAAGTCT | 50807 |
rs4733567 | snp | G/T | 0.0581099 | 0.160244 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052741 | tttgtttttgttttt[G/T]ttttttttttgAAAA | 50807 |
rs4733568 | snp | C/T | 0.459914 | 0.13578 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062390 | GTCTAGTCATATCTC[C/T]AAAAAAGTCAAAATC | 50807 |
rs4733569 | snp | C/T | 0.336474 | 0.234568 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086991 | CTCCTGCCTATTCCA[C/T]TCATCTTCCAAGGCT | 50807 |
rs4733570 | snp | C/T | 0.163564 | 0.234582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174307 | CTGGAAAGTGAAGCA[C/T]ATGTGTGAGTTCTGA | 50807 |
rs4733571 | snp | G/T | 0.483563 | 0.0891524 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278418 | GACCCTACCTAAAAA[G/T]GAACTGCACTTTTTG | 50807 |
rs4733572 | snp | A/T | 0.498133 | 0.030494 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287225 | CACAGTGCCTGGAAC[A/T]AGCAAATAATAGTTA | 50807 |
rs4733573 | snp | A/G | 0.336702 | 0.234484 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296635 | CCTCCTTCAACCTCA[A/G]ATCCTGCATCAAGGA | 50807 |
rs4733575 | snp | C/T | 0.321769 | 0.239477 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410017 | ATCTGGGTGTGAACA[C/T]AATGTCATAGGACCT | 50807 |
rs4733764 | snp | G/T | 0.478104 | 0.102316 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087383 | AAATCAGCTGGACAT[G/T]GTGGCGGGTGCCTGC | 50807 |
rs4733765 | snp | A/C/T | 0.640032 | 0.0992789 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088152 | ttattttttttgaga[A/C/T]ggagtttcgctcttg | 50807 |
rs4733768 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135151 | ACTCTAGGCTAGGCA[A/G]TCACACCCTTCATCT | 50807 |
rs4733769 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140304 | CCTCAAGTGAGATTA[C/T]AGGCGTGAGGCACCA | 50807 |
rs4733770 | snp | A/G | 0.476487 | 0.105846 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140419 | AATGTTTATTATGTA[A/G]GTAAACATGTGTCAC | 50807 |
rs4733771 | snp | A/G | 0.507946 | 0.227247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147681 | TAAAAGGCACATACA[A/G]TAAGATCCTGAATGG | 50807 |
rs4733772 | snp | A/G | 0.331874 | 0.236213 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162813 | ACAGAGGGAGACTCC[A/G]TCTCAAAAAAAAAAA | 50807 |
rs4733773 | snp | C/T | 0.357024 | 0.225933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174393 | CGAGGATGTCTCATT[C/T]ATCTCTTAGCCACTT | 50807 |
rs4733774 | snp | A/C | 0.356169 | 0.226336 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184437 | AGAGGGGCAGGCAGA[A/C]GGCCACTGTGTTTCC | 50807 |
rs4733775 | snp | A/G | 0.469642 | 0.119404 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201324 | CAAGGAAAAATGCAA[A/G]ACAAATTACACCATG | 50807 |
rs4733776 | snp | C/T | 0.497984 | 0.0316851 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216934 | CCCAGCAGTCTGGTA[C/T]CAACACAGCATCCAA | 50807 |
rs4733777 | snp | C/T | 0.469544 | 0.119585 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259316 | CTTTTAAATCTGTCC[C/T]CTTTTATTTTAGCTA | 50807 |
rs4733780 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284009 | ACAAAAACCTTGTGG[A/G]GGACTGGGTATGTGA | 50807 |
rs4733781 | snp | A/C | 0.462909 | 0.131034 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284521 | GAGGGCTGGGCTGAA[A/C]ATAAACTAAAAGGGA | 50807 |
rs4733782 | snp | A/C | 0.332799 | 0.23589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292143 | AAAATCTATAAAGAG[A/C]AGACTATAGGGAAAA | 50807 |
rs4733783 | snp | A/T | 0.347473 | 0.230215 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312781 | CCTAGCACAGAAATT[A/T]TCCCCCCTAGAAATA | 50807 |
rs4733788 | snp | A/G | 0.343254 | 0.231956 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324790 | ACATTCACATGGCCC[A/G]CATCTTAACCATGCA | 50807 |
rs4733793 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374605 | AAGCTTACATACTTG[A/T]CGACTTTAATAAAAT | 50807 |
rs4733794 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374607 | GCTTACATACTTGTC[A/G]ACTTTAATAAAATGC | 50807 |
rs5018867 | snp | C/T | 0.398894 | 0.200825 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107183 | CTCTCTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 50807 |
rs5021076 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300159 | ACACACACACAGAGA[C/G]AGAGAGAGAGAGAGA | 50807 |
rs5021077 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300157 | ACACACACACACAGA[C/G]AGAGAGAGAGAGAGA | 50807 |
rs5027392 | snp | C/T | 0.458545 | 0.137872 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409335 | AGTACAAAATCCCCA[C/T]GACCAATTCAAATGG | 50807 |
rs5895032 | in-del | -/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052751 | TTTTTTTTTTTTTTT[-/T]GAAAAAAACCAGTTT | 50807 |
rs5895033 | in-del | -/A | 0.34303 | 0.232046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055535 | AAAAAAAAAAAAAAA[-/A]GGCTGCTATGTACTA | 50807 |
rs5895034 | in-del | -/ACAG/AG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074486 | CACACACACACACAC[-/ACAG/AG]AGAGAGAACGAGAGT | 50807 |
rs5895036 | in-del | -/A | 0.477853 | 0.102875 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090297 | AGAGGATTAAAACTT[-/A]AAGAGAAATTTGGAA | 50807 |
rs5895037 | in-del | -/A | 0.497211 | 0.037236 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093788 | TACACTCTTCATATT[-/A]AAAAAAAAAAGTCTA | 50807 |
rs5895039 | in-del | -/T | 0.328616 | 0.237317 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113636 | GAGGTAGTTAACTGC[-/T]TTATAAGGAAAACTC | 50807 |
rs5895041 | in-del | -/CA/CACACC/CACC | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268535 | ACACACACACACACA[-/CA/CACACC/CACC]ACTGTGTAACTATAG | 50807 |
rs5895042 | in-del | -/A | 0.483923 | 0.0882034 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322304 | ATGCCATCTGTGGTT[-/A]AAAAAAAAAAAAAAT | 50807 |
rs5895043 | in-del | -/GAC | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342756 | CCAACTCTCAGAAAC[-/GAC]AAGTTAAAGTTGCTT | 50807 |
rs6415509 | snp | A/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079780 | TTTCTTGTTGTGGCC[A/T]GCCCCACTTGGCTGA | 50807 |
rs6415510 | snp | A/T | 0.399968 | 0.200024 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199433 | AATGGGGGAAGGGGC[A/T]AGATTCAGGAGAGGG | 50807 |
rs6415511 | snp | A/C | 0.352721 | 0.227922 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327735 | AGAAACAGAAAGTAG[A/C]TTAGTAAAGGATTTG | 50807 |
rs6415512 | snp | C/G | 0.385741 | 0.209939 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347623 | CCCCCAGGCTGAAGA[C/G]GAAGACTTAGCCCCA | 50807 |
rs6415513 | snp | C/T | 0.333491 | 0.235646 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355376 | TGTGCATTAGTGATC[C/T]AAAGAGCAAAAAAAG | 50807 |
rs6415514 | snp | C/T | 0.352504 | 0.228019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355651 | TGTGGTAATGTTAAG[C/T]CCCATATTTTTAAAG | 50807 |
rs6415515 | snp | C/T | 0.369754 | 0.219451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373111 | ACACAGAAATACATA[C/T]ACACACACACACACA | 50807 |
rs6415516 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377154 | atatgttctcactca[A/T]aagtgggagctaagc | 50807 |
rs6415517 | snp | C/T | 0.325799 | 0.238232 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386642 | ACAACTGTACCTCAC[C/T]CTGCAGAAACAGTTA | 50807 |
rs6470796 | snp | C/T | 0.450231 | 0.149691 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130052053 | GGAAGCCTTGATTCT[C/T]TCCTGTCAGCAGGGT | 50807 |
rs6470797 | snp | C/T | 0.449726 | 0.150364 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057573 | CCTGCCTTGGCCTCC[C/T]GAGTAGCTGGGACTA | 50807 |
rs6470798 | snp | A/G | 0.163564 | 0.234582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062899 | GGATTGCTTGAGCCC[A/G]GGGTCCAAGGCTACA | 50807 |
rs6470799 | snp | C/T | 0.462472 | 0.13174 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086800 | CAGAATAAGACCCTG[C/T]CTCAAAAACAAAGAA | 50807 |
rs6470800 | snp | G/T | 0.471578 | 0.115772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088714 | ggagcctcaggaaac[G/T]aatgcaGGTTTCTCC | 50807 |
rs6470801 | snp | C/T | 0.397994 | 0.201489 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111507 | ACAAATCCCCTAATT[C/T]ACATGATGCCAGTAA | 50807 |
rs6470802 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117196 | GAGTGCCAGGTCCTA[C/T]GGGACAGACACTGTT | 50807 |
rs6470804 | snp | A/C | 0.404733 | 0.196361 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133244 | CACACTGCCTTTTTC[A/C]GTCTAGACAGGCTAC | 50807 |
rs6470805 | snp | A/G | 0.495095 | 0.0492773 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149325 | AATTTGGTTCCCACA[A/G]TTCTGCATTACTTTG | 50807 |
rs6470806 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195295 | AATCCAAGCAATTGG[C/G]GGGGGCCAAGGTGTG | 50807 |
rs6470807 | snp | A/G | 0.495596 | 0.0467178 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216048 | aaaaaggaaaggaaa[A/G]gaaagaaaaggaaaa | 50807 |
rs6470810 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249225 | GTCTAGTCATGCCAC[C/T]CTCTGACTTTAAAAC | 50807 |
rs6470811 | snp | G/T | 0.487684 | 0.0775019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326687 | ATGTAAATGTTCAAG[G/T]GTTCTACACTTTGAA | 50807 |
rs6470812 | snp | A/G | 0.475437 | 0.108066 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328019 | CCCACTTTTGCAAAA[A/G]AAAAATATATATATA | 50807 |
rs6470813 | snp | C/T | 0.354019 | 0.227333 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330018 | GCTTTCAGGGAGAGA[C/T]AGTTGTAATCTAATT | 50807 |
rs6470814 | snp | A/G | 0.332799 | 0.23589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333820 | GGCCTATTATGTGAC[A/G]AGCAGCATGCAGAAT | 50807 |
rs6470815 | snp | C/T | 0.493386 | 0.0571263 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335553 | AATATGAAGAGATCA[C/T]GATTCAAAGCCAGAA | 50807 |
rs6470816 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337469 | GAGCCCTGTTATAAA[C/T]TGTAAATTCTGAACG | 50807 |
rs6470817 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414956 | agagacaggatttca[C/T]catattggtcaggct | 50807 |
rs6470818 | snp | A/G | 0.121022 | 0.21416 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417509 | GCAGTCCCTTCTCAC[A/G]GTTCAGAGATTGTTG | 50807 |
rs6470819 | snp | A/G | 0.305436 | 0.243776 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423926 | GGAAAATGGGGGGTG[A/G]CTGCTAATGAGTATG | 50807 |
rs6470820 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423993 | TCTAAAATTGACTGC[A/G]GCGATGGCTGCACAA | 50807 |
rs6980501 | snp | A/G | 0.497473 | 0.0354532 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414218 | GACCTTTCATTGGAC[A/G]AATGTTTGCTGACCC | 50807 |
rs6981371 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130994 | accccatctctacta[A/C]aaacacaaaaaaatt | 50807 |
rs6981372 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130997 | ccatctctactaaaa[A/T]cacaaaaaaattagc | 50807 |
rs6981861 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284057 | TAGACTCATCATCAT[C/G]ACATCCGCCTTAAAT | 50807 |
rs6982030 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284162 | ACCGAATGTGTAGGG[C/T]GTCTTGAAAATTTGG | 50807 |
rs6982081 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131389 | AACTAAGGCTTCCCT[C/T]TGAGGCATGTGCTTT | 50807 |
rs6982649 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423445 | acttgaaaatgtgcc[C/T]accctttgtccctga | 50807 |
rs6982661 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086518 | CCTGTATTAAGAATT[C/T]ATGggctgggtgtgg | 50807 |
rs6982831 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088536 | ggctgcaccactcca[C/T]ggatcacctggagtc | 50807 |
rs6983271 | snp | G/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410609 | GCCTAGGGTCTGCTG[G/T]GCTGCCCATTGTGTG | 50807 |
rs6984045 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080167 | TTTGCGGTTTTTTAT[C/T]TCTGGTAAAGGAGTG | 50807 |
rs6984815 | snp | A/G | 0.369346 | 0.219673 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143825 | TGGAAGTGTAAAGTT[A/G]TTAGCACAGGCATAT | 50807 |
rs6984963 | snp | A/G | 0.45843 | 0.138046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319850 | ttttaatgacatgac[A/G]aaaaaactttctagg | 50807 |
rs6985541 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445096 | AATTCTCTCTCCGTG[A/G]CCAGAAGCAGTAGGA | 50807 |
rs6985563 | snp | C/T | 0.464629 | 0.128197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320098 | atgagaaaTTACTTA[C/T]AATGTTCtttaaaaa | 50807 |
rs6986119 | snp | G/T | 0.409041 | 0.192888 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408183 | TAGCAACCCCTTATT[G/T]TTGttttatgtgtca | 50807 |
rs6986163 | snp | A/G | 0.409212 | 0.192748 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408412 | tttgctctctgcttg[A/G]gctgggacatgcatc | 50807 |
rs6986746 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284605 | CAATGGCTTCCTTTG[A/G]TTTGGGAACCAGTGA | 50807 |
rs6988261 | snp | C/T | 0.491783 | 0.0635686 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175515 | ataggtgtgagccag[C/T]acacctggACtgttg | 50807 |
rs6988276 | snp | A/T | 0.359787 | 0.224604 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175543 | ttgttgagttttttt[A/T]atatattctggatat | 50807 |
rs6988422 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353785 | cagaggtgagagaat[C/T]gcttgaacctgggag | 50807 |
rs6989356 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111261 | ggtgccacacacctg[G/T]ggttccagctacttg | 50807 |
rs6989965 | snp | C/G | 0.0648419 | 0.167978 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084553 | GTTTGTGGAAAGAGA[C/G]GGGGCATTGGCTCAG | 50807 |
rs6990443 | snp | A/G | 0.316485 | 0.240998 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385928 | ttcaacctctccctg[A/G]agtctgggaatgatc | 50807 |
rs6991291 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173384 | GACAGAGAGCCACCA[C/T]GACCTGCCAAAACAT | 50807 |
rs6991382 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138370 | AGTGAGAGACCCCAG[A/G]GGATTCCATGTTCAA | 50807 |
rs6991549 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203404 | TCCCCTCACTAACCC[A/G]TGTTTCCCGGTGCTG | 50807 |
rs6991714 | snp | A/G | 0.342358 | 0.232314 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173458 | TCTCTGTTTTAGCTC[A/G]TCCTAGTTCAGTGGA | 50807 |
rs6991810 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291421 | ACTGTCCTCACTAAG[C/G]GGAAAGGTCTGCTGA | 50807 |
rs6991855 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315789 | AGAAAAAAAGCAACA[C/T]TGAGCACCCAAACCA | 50807 |
rs6991975 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102651 | gtcttcaattttttt[A/G]gaacagtttaagaat | 50807 |
rs6992032 | snp | A/G | 0.351418 | 0.228505 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072793 | ggacttgcaattgat[A/G]tgtgtgtgtgtgtgt | 50807 |
rs6992094 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278561 | CAAAAGTCTTCCATG[A/C]AAATAAGCCTTTCTC | 50807 |
rs6992270 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336970 | TAGTATAAAAATAGT[C/T]TTGATCTCTCAGAAC | 50807 |
rs6992305 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102841 | caggtaggtaccacc[A/G]tgcccaagtaatttt | 50807 |
rs6992421 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163287 | AAACAAGGATTCAGA[A/C]ACTAACAACTTATAA | 50807 |
rs6992854 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133392 | CCGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 50807 |
rs6993913 | snp | A/C/T | 0.0115206 | 0.075079 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246088 | CTCAATTAATCACTG[A/C/T]GAGTTGTAAAGGAAG | 50807 |
rs6993944 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391745 | TCATTTCAGTCCAAT[A/T]CAGTAAATGTAATAA | 50807 |
rs6994242 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364052 | CTCGTGCAATTTCAG[G/T]TAATAATAATAATTA | 50807 |
rs6994477 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391807 | AGAGAGAGCTCCTGT[A/G]ACAATCCCAGGCCAG | 50807 |
rs6994854 | snp | A/G | 0.468349 | 0.121752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392077 | CTCATCTGGTTTGCA[A/G]ACTTCTTGAGGGGAA | 50807 |
rs6995074 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392356 | GAATAAGACATCTAA[C/T]AGGGAAAAGGGATGT | 50807 |
rs6996001 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108936 | aggcgccactacgcc[C/T]ggctcattttgtatt | 50807 |
rs6996027 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417117 | ATACACACAGAAGTG[A/C]AACCCATGTACAACT | 50807 |
rs6996058 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129905 | AAGATTAAAACAGTA[A/T]TTTTTATATCAGTCT | 50807 |
rs6996106 | snp | A/C | 0.340108 | 0.233197 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086249 | TGAATCCTGGCCCCC[A/C]CGTACTAGCTGTGAG | 50807 |
rs6996422 | snp | C/G | 0.499053 | 0.0217445 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109006 | TCTCGAACTCCCGAC[C/G]TCAGGTGATCCGGCC | 50807 |
rs6996435 | snp | C/T | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086361 | TGAGGTACGTTAACA[C/T]ATGCGAAGTGCTCAA | 50807 |
rs6996469 | snp | C/T | 0.352287 | 0.228117 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255381 | TGTACATTTTCTCTA[C/T]GTACCTAATAAATGT | 50807 |
rs6996788 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352372 | GCAAGGGGAGCTGAC[A/G]AACAAGATCAGACGT | 50807 |
rs6998031 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279885 | TTGCCTCTCTTGAAC[A/C]AATAATCAATATAAA | 50807 |
rs6999216 | snp | A/T | 0.35809 | 0.225425 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355765 | CTATGGTGGCTATCC[A/T]TCAGTAAAAAAACCT | 50807 |
rs7000069 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130180096 | ggaaagagaaagaga[A/G]ggagggaatagagag | 50807 |
rs7001981 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441187 | GCAGGACTGGCACCT[C/T]CCACAGGGAAGCCAC | 50807 |
rs7002892 | snp | A/T | 0.433382 | 0.169915 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222889 | ACTAGTGTACTTGGT[A/T]AAGTGCAGGAGCCTC | 50807 |
rs7003309 | snp | A/C | 0.4021 | 0.198407 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097860 | TGAGAATATCTCCCC[A/C]AACAGTACTCAGCAA | 50807 |
rs7003541 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149041 | tttgtagagataggg[A/T]ttctccatgttgccc | 50807 |
rs7003568 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097846 | CTATGAAGGTGGTTT[A/G]AGAATATCTCCCCCA | 50807 |
rs7004723 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201579 | GCATTATCTGCAGCA[C/T]CTGATTTCATTTGAC | 50807 |
rs7004884 | snp | A/G | 0.386504 | 0.209444 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123023 | TCATGGTAGTTTTAC[A/G]ATCAAATTAACTTTT | 50807 |
rs7005039 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366249 | AATTGCCTACTATTT[A/T]AAAATTGTAACAGTA | 50807 |
rs7005271 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366179 | CCTTCAGAAACTCCC[A/G]TCTACAACAGATTAT | 50807 |
rs7006336 | snp | A/G | 0.34146 | 0.23267 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140821 | AGGAGCCAAGTACGC[A/G]TAAGTTTTGACTGTC | 50807 |
rs7006481 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323774 | ATGCTAGGCACTCAG[C/T]AGATCTTTGATAAAC | 50807 |
rs7006600 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353779 | aggaggcagaggtga[C/G]agaattgcttgaacc | 50807 |
rs7006658 | snp | C/T | 0.2776 | 0.248472 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189530 | attgtgtatatatac[C/T]gtattttctttatct | 50807 |
rs7006802 | snp | C/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198785 | ggccactctcatttc[C/G]tctgtgctctgctgt | 50807 |
rs7007010 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198953 | ACCCATTCTCACTGC[A/G]CTACAACTCCTTTTG | 50807 |
rs7007359 | snp | C/G | 0.431621 | 0.171796 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381845 | tggaatgccctgcac[C/G]caggcctctgcatgc | 50807 |
rs7008180 | snp | C/G | 0.198324 | 0.244601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075532 | GGCCCTGAGCTCCTC[C/G]GAGCTTCCGTCTGTA | 50807 |
rs7008182 | snp | A/T | 0.49681 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332499 | ATAATACAAAGAACA[A/T]CTAATTTTACTTCAA | 50807 |
rs7008507 | snp | A/T | 0.394354 | 0.204112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149843 | GATTATGAGTGATGT[A/T]ACTGGCAGCAAAAAA | 50807 |
rs7009083 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159405 | aggtgggcagatcac[A/G]aggtcagaagatcga | 50807 |
rs7010399 | snp | A/T | 0.445592 | 0.155704 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425021 | aaataaataaataaa[A/T]aaaAGAGTGGACAAA | 50807 |
rs7010678 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115133 | gtctagatgttgctg[C/T]aaaggaattttttag | 50807 |
rs7011509 | snp | A/G | 0.430136 | 0.173352 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388390 | gcagcatgagctgca[A/G]gaggagtgaggagaa | 50807 |
rs7011658 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199549 | TCTGGCAAGAagaga[A/G]gaaagaatgaaggtc | 50807 |
rs7012283 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072788 | ggcctggacttgcaa[C/T]tgatatgtgtgtgtg | 50807 |
rs7012705 | snp | A/C | 0.479663 | 0.0987666 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177234 | AGCTATACAAGTTAG[A/C]ATCACCATTACTAGC | 50807 |
rs7014098 | snp | C/T | 0.315273 | 0.241329 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391604 | CACCTAGGCAGGTAC[C/T]AGGGGACAGGAGAGG | 50807 |
rs7014715 | snp | C/T | 0.163892 | 0.234703 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186232 | AACGTTTTTGTTCTC[C/T]GCTGCATTTAGAACT | 50807 |
rs7014800 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195426 | GGGCATGATGGCGCA[C/T]GCCTGTAGTTTCAGC | 50807 |
rs7014892 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195299 | caagcaattggcggg[A/G]gccaaggtgtgggaa | 50807 |
rs7015970 | snp | C/T | 0.498415 | 0.0281103 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085916 | ACTTCAGTAATGTAA[C/T]GCTGGGGCTATTTTG | 50807 |
rs7016144 | snp | A/G | 0.429987 | 0.173507 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388642 | gactgagagggtaga[A/G]tcacaagaagaaatc | 50807 |
rs7016413 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331203 | GGGGCATGGCTATTT[C/T]GAGTGGAAAGAGCGA | 50807 |
rs7016780 | snp | A/C/G | 1.64817e-05 | 0.00287064 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054693 | AAGGCAGCAGTCTTG[A/C/G]ATGAAGGATGTGGAC | 50807 |
rs7017024 | snp | G/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054692 | GAAGGCAGCAGTCTT[G/T]CATGAAGGATGTGGA | 50807 |
rs7017089 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419312 | AAAACCATCCCCATC[A/G]TCTGCCACTAATTAC | 50807 |
rs7017795 | snp | A/G | 0.20511 | 0.245937 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201033 | CAATATCACCTGGAA[A/G]CTTGTTGGTTATGAA | 50807 |
rs7018225 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349231 | GTGTTTGGTGTTGCC[C/T]TAGTCCTCTCCTTAG | 50807 |
rs7018391 | snp | C/G | 0.258843 | 0.249844 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231260 | GAGACAAAAATGTAA[C/G]GAAATGAGAAAATCA | 50807 |
rs7357470 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074113 | TCAAACAAACAAGTT[C/T]TTAAAAAAAAAAAGG | 50807 |
rs7386417 | snp | C/T | 0.455858 | 0.141853 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071607 | gtagctgagagtaaa[C/T]aaataaatgggcaaa | 50807 |
rs7386870 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417887 | ctgtactggtggttc[C/T]aataaaagtctcagg | 50807 |
rs7387355 | snp | A/G | 0.351853 | 0.228311 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064464 | aaggaacagtctgga[A/G]tggagccggagtccg | 50807 |
rs7387699 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326783 | AAAGCAAAGCATTAA[C/T]TTAATGCTTCTCTCC | 50807 |
rs7459933 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156175 | AGCATTCCAAAGCTA[C/G]GGTCAAAAATTACCA | 50807 |
rs7460225 | snp | C/T | 0.459118 | 0.137002 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327127 | TGTTGGTAGGGCACT[C/T]TATCTTTCTGAGCAG | 50807 |
rs7460645 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061778 | TTACTATGTTTAGGA[A/G]AGCTCCAAATCAGTT | 50807 |
rs7460858 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421023 | AACAtacagtatagc[C/T]actaagcaggcaggc | 50807 |
rs7462179 | snp | A/C | 0.498009 | 0.0314867 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133668 | ACTCCGTCTCAAAAA[A/C]AAACAAACAAACAAA | 50807 |
rs7462286 | snp | C/T | 0.327445 | 0.237702 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155068 | CAGTGTCATCCTAAA[C/T]ATCAAACACTCAATC | 50807 |
rs7462417 | snp | C/T | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063586 | GGGAAAGAGAGGAGA[C/T]TGGCCTTCTTGAGAC | 50807 |
rs7462977 | snp | A/G | 0.0729998 | 0.176553 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410832 | CTGATCTTGAGTGAT[A/G]AAAAATCACTTCTGG | 50807 |
rs7463793 | snp | A/G | 0.127944 | 0.218179 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441710 | TTGAAAATCTGGCTC[A/G]CTGTGGCTGGTGAGG | 50807 |
rs7463951 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229314 | TGACTGCTTGTTAGA[A/G]GTTGTCATGGCATGG | 50807 |
rs7464740 | snp | A/C | 0.20511 | 0.245937 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443223 | GGAGACCTCCCCCCC[A/C]CACCGGGCGGCCTCG | 50807 |
rs7464885 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166989 | CCTGAAGTGCATGTC[C/T]TCAAAACTAGGATTG | 50807 |
rs7465238 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145899 | cagggtggggtacgg[G/T]ggtgtgatctcggct | 50807 |
rs7812299 | snp | C/T | 0.409382 | 0.192607 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405225 | CCTCCTTGGTGCCAG[C/T]TGGACTCACACAACA | 50807 |
rs7812469 | snp | C/T | 0.408871 | 0.193029 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405327 | GTCCAAGACAGTGTG[C/T]GGCAGAACTAAGATC | 50807 |
rs7812798 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343704 | tacacaaatattcac[C/T]gctccaaggtgaaca | 50807 |
rs7813167 | snp | C/T | 0.311123 | 0.242413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364973 | AACACAAAAAACAAA[C/T]GCCAAACAAACAAAC | 50807 |
rs7813441 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152100 | AAATGCTCATCTCTC[A/T]TTTCTACTATTCTGC | 50807 |
rs7813449 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188787 | tggtgtagctccaga[A/G]cttgtgttcttaaac | 50807 |
rs7814745 | snp | C/T | 0.116138 | 0.211142 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419678 | GCTACAGGGTGGTTT[C/T]AGCAACAGGGAGCCC | 50807 |
rs7815166 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419942 | CTACATCTGCCTGCA[C/T]CACCTTCTTCTTCtt | 50807 |
rs7815532 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272274 | aaaatgcaatttaaa[A/C]ccataatgacatatc | 50807 |
rs7815718 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444509 | ATGTATATTGTGCAT[A/G]TCTATGTCTACTTTC | 50807 |
rs7816255 | snp | A/G | 0.470811 | 0.117228 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083858 | GAGTACAACGGCATC[A/G]TCTCAGCTCACTGCA | 50807 |
rs7816470 | snp | A/G | 0.120326 | 0.21374 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414950 | tttagtagagacagg[A/G]tttcaccatattggt | 50807 |
rs7816581 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113907 | ccacctctgcctccc[C/G]ggcagctgggaccac | 50807 |
rs7816822 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253137 | CACATAGCTACCAAC[C/T]AGATGCTGGAATTTA | 50807 |
rs7816836 | snp | A/G | 0.382279 | 0.212137 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414978 | ggtcaggctagtcac[A/G]aactcctgacctcag | 50807 |
rs7817038 | snp | A/G | 0.120326 | 0.21374 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415337 | gtggggtgtggtggt[A/G]tacacctatagtccc | 50807 |
rs7817803 | snp | A/C | 0.474272 | 0.110462 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307576 | TTCTCCCCAACACCC[A/C]ACAGGTAACCACCTT | 50807 |
rs7817849 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423513 | ggacaagtatgtaca[A/T]gcaaaaactagaaac | 50807 |
rs7818165 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162094 | tgtgagcaccatgct[C/T]gaccTAAATGTTCAC | 50807 |
rs7818168 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162098 | agcaccatgctcgac[C/T]TAAATGTTCACTTTT | 50807 |
rs7818185 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162130 | ATCAGGGCCTATAGC[C/T]TTGAATTCTATAGTA | 50807 |
rs7818718 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373015 | acacagacacacata[C/T]acacagacacacaca | 50807 |
rs7818960 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372999 | gcacagacatacaca[C/G]acacagacacacata | 50807 |
rs7818969 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373005 | acatacacagacaca[C/G]acacacatacacaca | 50807 |
rs7818977 | snp | C/G | 0.277334 | 0.248501 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373021 | ACACACATACACACA[C/G]ACACACACACACATA | 50807 |
rs7818996 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373059 | acagacccacacaca[C/G]acacagacataagca | 50807 |
rs7820841 | snp | A/T | 0.213635 | 0.247341 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107511 | ttttttttttttttt[A/T]aaaaatgtatgtatg | 50807 |
rs7821176 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202847 | TTTCAGTTGCTTAAC[A/G]TATCTGTGGCAATAT | 50807 |
rs7821366 | snp | A/G | 0.304438 | 0.244001 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415720 | ttgaacccaggaggc[A/G]gaggttgcagtgagc | 50807 |
rs7821440 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057438 | TCTTGACCTGTCTTC[A/G]AAGCCCCATGGCTGt | 50807 |
rs7821742 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233220 | TCATCCCACAGGTTA[C/T]AATGCTGGGATTTTC | 50807 |
rs7822048 | snp | C/T | 0.46885 | 0.12085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378995 | acagaactcttgcag[C/T]ctcctgagtggtaag | 50807 |
rs7822125 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345586 | AGGTGGGGGCTATGG[A/G]GCCAGGCAAACCCAG | 50807 |
rs7822259 | snp | A/G | 0.331179 | 0.236453 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409374 | GGTCTTTCAGTTTCC[A/G]TATCTGCTGGCAAGC | 50807 |
rs7822764 | snp | A/G | 0.173965 | 0.238157 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102600 | tggtattagggcaat[A/G]ctggcctcattggaa | 50807 |
rs7822957 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403616 | ggagtgcagtggcgc[A/G]atcttggctcattgc | 50807 |
rs7823146 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403759 | gggtttcgccatgtc[A/G]agcaggctggtctcg | 50807 |
rs7825499 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166585 | GCAGTCATCTTCCAA[C/T]GTATCTCTAATAGTA | 50807 |
rs7825930 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386524 | CAGGGCTAAGCGCTG[C/T]GCTCTCCACCCTGTA | 50807 |
rs7826083 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108626 | CAATGTGGTGAAACC[C/T]TGTCCCTACTAAAAA | 50807 |
rs7826256 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263997 | CTGACAACTTAGGTT[C/T]TAGCCCCTGTTAAAA | 50807 |
rs7826415 | snp | G/T | 0.348354 | 0.22984 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099700 | ttttttttttttttt[G/T]gagacagagtcttgc | 50807 |
rs7826683 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146193 | GGAATGTGGGCAGGA[A/G]GTAACATCACAGCTG | 50807 |
rs7827068 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195273 | AGGAATggtggctca[G/T]gcctgtaatccaagc | 50807 |
rs7828689 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375286 | AATATTCTATTGGCC[A/G]CTGCAGGAATGGGCC | 50807 |
rs7828824 | snp | A/G | 0.409382 | 0.192607 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405397 | TCTGCATAAATCATA[A/G]AAGGGTCTTGCAGAT | 50807 |
rs7828842 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222424 | ATCCTGAAACTCATG[C/T]GATACTCCCTCAAGG | 50807 |
rs7830887 | snp | A/C | 0.163564 | 0.234582 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086760 | agtgagctatgatca[A/C]gccactgcactccag | 50807 |
rs7832287 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222534 | ATCCTTCTCCACTGA[C/T]ACACTCAGGAAAGAC | 50807 |
rs7832651 | snp | A/G | 0.499703 | 0.0121769 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252972 | AGTTTGGAAACCACC[A/G]AGCCTTTTAGCTTCC | 50807 |
rs7832716 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097659 | GCAGAAGTGACTATG[C/T]TCACCCTGGCAGGCC | 50807 |
rs7832888 | snp | A/G | 0.467234 | 0.12373 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375869 | CAGCTGTCTACAGCC[A/G]TACCTTTGCTGATGT | 50807 |
rs7833007 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095947 | TTAAGGAGGCCAATA[C/T]GTTTCACTTAGGTTG | 50807 |
rs7833272 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165449 | CTTACACTGAGAAAT[C/T]ATTCAAAGAGACCAC | 50807 |
rs7834461 | snp | C/T | 0.498871 | 0.0237351 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231703 | AAAAGATTAACATTT[C/T]CAACCTAATTCATTT | 50807 |
rs7834677 | snp | C/G | 0.221439 | 0.248363 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423773 | ataattatggatgat[C/G]attatttgcttcttt | 50807 |
rs7834860 | snp | C/T | 0.131381 | 0.220067 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423992 | TTCTAAAATTGACTG[C/T]GGCGATGGCTGCACA | 50807 |
rs7836266 | snp | C/T | 0.164873 | 0.23506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101766 | ttgcagagatagggt[C/T]tcaccatgttgccca | 50807 |
rs7836273 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381673 | aataaaatctactcc[C/T]atgacttagtctaaa | 50807 |
rs7836536 | snp | C/T | 0.163892 | 0.234703 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197035 | GCATGTGGCCACTCA[C/T]CACTCCCGGCCTGCG | 50807 |
rs7836688 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229132 | AAACCAGTTCAGAAT[C/T]AGCAACAATCTGCTT | 50807 |
rs7836994 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373013 | agacacagacacaca[C/T]acacacagacacaca | 50807 |
rs7837226 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223649 | TGATGGGGTTATTAA[A/G]GGAAATAGATGAGAA | 50807 |
rs7837833 | snp | A/C | 0.320096 | 0.239972 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106025 | GCTTCCCTTTCCACA[A/C]CCTGGCAGTCAGGTG | 50807 |
rs7838372 | snp | G/T | 0.163892 | 0.234703 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166444 | GTCCTCCGTAGTCAG[G/T]TCTGAGTTTTTACCT | 50807 |
rs7838539 | snp | A/G | 0.406641 | 0.194842 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400207 | ACCCACACACTTTCC[A/G]CTACGCGGACTTCTT | 50807 |
rs7838650 | snp | C/T | 0.406641 | 0.194842 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400208 | CCCACACACTTTCCA[C/T]TACGCGGACTTCTTA | 50807 |
rs7838861 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359553 | GGCTGAGCCTGTCCT[C/T]TGCGACACACACCCA | 50807 |
rs7839088 | snp | C/T | 0.115438 | 0.210697 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415553 | agcactttgggaggc[C/T]gaggctggtggatca | 50807 |
rs7839155 | snp | A/G | 0.470327 | 0.118136 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306623 | AACCTTAGGGCACAA[A/G]CGGAACAAACTCAGC | 50807 |
rs7839214 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415618 | catggtgaaacccca[C/T]ttctacgaaaaatac | 50807 |
rs7839523 | snp | G/T | 0.462253 | 0.132093 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269580 | AGTTTCATACTGACA[G/T]AGTGGTCATCTCAGC | 50807 |
rs7840060 | snp | C/G | 0.444444 | 0.157135 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300153 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 50807 |
rs7840188 | snp | A/G | 0.115788 | 0.21092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418288 | ggcacggtcgcacac[A/G]cctgtaatcccagca | 50807 |
rs7842504 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400558 | tttgggaggccgagg[C/T]gggcagatcacgagg | 50807 |
rs7843126 | snp | A/G | 0.348794 | 0.229651 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099967 | gtaaatagcactgca[A/G]taaacatggggtgca | 50807 |
rs7844582 | snp | C/T | 0.316968 | 0.240864 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379628 | aggaaaattggagaa[C/T]tgcttggtatagaga | 50807 |
rs7846376 | snp | A/G | 0.411074 | 0.191194 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143197 | ATGACACTTTTCAAA[A/G]CTGACAATTCTACAA | 50807 |
rs7846662 | snp | C/T | 0.355096 | 0.226837 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231399 | ACTGTCATTTTTTTC[C/T]TGCCCAGAAATATTA | 50807 |
rs9297805 | snp | C/T | 0.409212 | 0.192748 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229050 | AATGCAACAGACAAA[C/T]TAGCCGAGCAAAGTC | 50807 |
rs9297806 | snp | C/T | 0.337614 | 0.234145 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346366 | TGTCAGGAAGTTCTT[C/T]TGAGTCTAACCTACA | 50807 |
rs9297807 | snp | C/T | 0.409382 | 0.192607 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406584 | tcacccaggttcaag[C/T]gattctcctgcctca | 50807 |
rs9643252 | snp | A/G | 0.469445 | 0.119766 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320421 | ATTAGCTGGTGTGGT[A/G]GTACTTGTCTGTAGT | 50807 |
rs9649962 | snp | A/G | 0.16028 | 0.233346 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376396 | CTGTATGCAGCTGGA[A/G]CAAGAAGAGCATGGC | 50807 |
rs9693372 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373031 | acacagacacacaca[C/T]acatacacacataca | 50807 |
rs9693383 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372969 | GCATATACACACACA[G/T]ACATACACACATACG | 50807 |
rs9693386 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373090 | cacacagacaccccc[A/C]cacacacacagaaat | 50807 |
rs9694314 | snp | C/T | 0.243061 | 0.249904 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368852 | tgttagtccaaccct[C/T]ggacttcctagtaat | 50807 |
rs9694613 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373109 | acacacagaaataca[C/T]atacacacacacaca | 50807 |
rs9773235 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417201 | gtacaactgcacaca[C/T]acagaaaacaaccca | 50807 |
rs9942745 | snp | A/G | 0.256619 | 0.249912 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101167 | caccaatacaaagct[A/G]ttctggttactatag | 50807 |
rs9942820 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100983 | tattatgtttaagtc[C/T]ttaattcatcttgag | 50807 |
rs10085959 | snp | C/T | 0.138207 | 0.223612 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194710 | tcaacctaagtccct[C/T]acattcacagttcac | 50807 |
rs10086454 | snp | C/T | 0.407158 | 0.194426 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399003 | acttcccagccttct[C/T]tgccgcaaaatgtag | 50807 |
rs10086773 | snp | C/T | 0.473414 | 0.142873 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408442 | cttcttttttggaca[C/T]tggcgctcctggttc | 50807 |
rs10087287 | snp | A/C | 0.296619 | 0.245615 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395708 | gtctcactctgtcac[A/C]caggctggagtgcag | 50807 |
rs10087626 | snp | C/T | 0.244776 | 0.249945 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395908 | tgatcttaggtaatc[C/T]gcccgcctccgtctc | 50807 |
rs10087951 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204114 | gtgagttgcgggcta[C/T]tgagcgaagctgagt | 50807 |
rs10088554 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228761 | AAAAAACCTTTAACT[G/T]GAAAAATATATAAAC | 50807 |
rs10088575 | snp | A/C | 0.140242 | 0.224618 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082613 | ggctcaaatgatcct[A/C]ccgcctcagcctccc | 50807 |
rs10089819 | snp | C/T | 0.409382 | 0.192607 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160722 | CGTTGAACTGCAGAA[C/T]GAGAACATGGTCTTT | 50807 |
rs10090106 | snp | A/G | 0.409041 | 0.192888 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401710 | GAAAACATAGTAGGC[A/G]GTCTACACCTGTACA | 50807 |
rs10090231 | snp | A/G | 0.389261 | 0.207621 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401837 | GAAGAATCCCGCTGT[A/G]TCTCCCACGCCGAGT | 50807 |
rs10090767 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402011 | GGACAAGAGTCATCC[A/G]GTGAAACTGGGCAGA | 50807 |
rs10091130 | snp | C/G | 0.352084 | 0.228208 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361641 | ACTGGTCTGCAATTA[C/G]AATTTCAAAGGTTCA | 50807 |
rs10091313 | snp | A/G | 0.491936 | 0.0629843 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213846 | AAGTGTGCACATGGT[A/G]TGAGGGCTGGGGAGG | 50807 |
rs10091450 | snp | C/T | 0.395453 | 0.203331 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234776 | TGCAGCTCACAAGCA[C/T]AGAGCCTCAGGTACA | 50807 |
rs10092647 | snp | A/C | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444846 | TCATTGTGGTTTCCC[A/C]CGGAAATGCCACATT | 50807 |
rs10095631 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130062127 | AGGGTTCTTTAAGGC[A/C]CTATTACAGTATTAC | 50807 |
rs10095984 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176019 | GGAGGATATGTCTGT[C/T]TGGAAAGCAGCATGT | 50807 |
rs10096176 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245502 | CAAAAATTTAACATA[C/G]CACCTTCGACCAATA | 50807 |
rs10096261 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090337 | ATTTGTGATATGAAA[C/T]GCTGATGTGAAACTT | 50807 |
rs10097893 | snp | C/T | 0.136506 | 0.222754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194527 | GTGTTTTCACTTCTA[C/T]AGTTCTTTCAGGAAT | 50807 |
rs10098244 | snp | A/G | 0.124837 | 0.216412 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403589 | gagacagtttcactc[A/G]ttgcccagactggag | 50807 |
rs10098396 | snp | C/T | 0.420892 | 0.182472 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434004 | GTATTGAACACAGAT[C/T]GCCTTGCTTAAAATC | 50807 |
rs10098622 | snp | A/C | 0.402277 | 0.198272 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434176 | caaaaattaactgtg[A/C]ctggtggcgcacacc | 50807 |
rs10099391 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266974 | tgaggataagagaca[C/T]agaagatagaatgag | 50807 |
rs10099549 | snp | C/T | 0.425123 | 0.178415 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398939 | tctcttcttctataa[C/T]aataactctcaattt | 50807 |
rs10099586 | snp | A/G | 0.407158 | 0.194426 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399058 | agaatataagtagga[A/G]caggaggtgcaactt | 50807 |
rs10099820 | snp | A/G | 0.114387 | 0.210022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121175 | gtccagtttaccttc[A/G]gcgctcagtggatct | 50807 |
rs10100892 | snp | C/T | 0.383824 | 0.211166 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224775 | GCCATCAAAACACAA[C/T]GCTACAATAAATACT | 50807 |
rs10101611 | snp | C/T | 0.139225 | 0.224118 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066584 | tcttttttctttctt[C/T]cttctctctctctcc | 50807 |
rs10103052 | snp | C/T | 0.168785 | 0.236441 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213467 | TAAACTAACCTTTTG[C/T]ATCTAATGGATTATG | 50807 |
rs10103132 | snp | C/T | 0.406986 | 0.194565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396415 | ACAAGACCAGCATCA[C/T]CACTTCCCATCTCTC | 50807 |
rs10103280 | snp | A/G | 0.379354 | 0.213933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405499 | GAGGCTGCTGGGGTC[A/G]GGGGGAAGGCCACTG | 50807 |
rs10104573 | snp | C/T | 0.139225 | 0.224118 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139597 | AGCTAAGCATGACGG[C/T]GCATGCCTGTAATCC | 50807 |
rs10106205 | snp | C/T | 0.195526 | 0.243993 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068165 | ggggcactggatgca[C/T]aaagaaatgcaaact | 50807 |
rs10107054 | snp | A/T | 0.409552 | 0.192466 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406571 | actgcaacctccgtc[A/T]cccaggttcaagcga | 50807 |
rs10107675 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336122 | GCAAAACAAAGTTTC[A/T]GAAACAGCCCTGTGA | 50807 |
rs10109236 | snp | C/T | 0.346147 | 0.230772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345145 | TTGCCTAACAAAGTG[C/T]TGTGTGGACGAAATG | 50807 |
rs10109827 | snp | A/T | 0.164219 | 0.234823 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102558 | tggctggtagttttc[A/T]ttttttgttgtgtcc | 50807 |
rs10111650 | snp | A/G | 0.242201 | 0.249878 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394755 | TTTATTTCTCAACCC[A/G]GCCAACGCTTAGGGA | 50807 |
rs10112253 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277328 | CGGCTATAGGCAACA[A/G]GAGAAAAACACCAAT | 50807 |
rs10113410 | snp | A/G | 0.481242 | 0.0950111 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089397 | TTTTACTACCTGCTC[A/G]TGCCTGGTGTCTACC | 50807 |
rs10113820 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224835 | tttatctctggaaaa[A/G]tatcttcacaaaagc | 50807 |
rs10505547 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116530 | ATTTTACCACTTTTT[C/G]TAATGTAGCACATTG | 50807 |
rs10505548 | snp | A/G | 0.35809 | 0.225425 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258208 | AAGACGTTAGGGCAC[A/G]TTTAGATGCTTGAGG | 50807 |
rs10505549 | snp | G/T | 0.334182 | 0.235401 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266372 | GGGAATCATATCAGT[G/T]ACTTAATCTCAAATA | 50807 |
rs10538783 | in-del | -/ACAG | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417234 | TACAACTGCACACAT[-/ACAG]ACAGACAGATATACA | 50807 |
rs10544429 | in-del | -/ACAG | 0.273049 | 0.248935 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372966 | CAGGCATATACACAC[-/ACAG]ACATACACACATACG | 50807 |
rs10547542 | in-del | -/AG | 0.46137 | 0.133501 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299687 | AGAATTTAAAGAAAC[-/AG]AGAGATCAAGAAGAC | 50807 |
rs10568607 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108786 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAGATGGAGTTTCAC | 50807 |
rs10576537 | in-del | -/TC | 0.193653 | 0.243567 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079024 | CATGCTGAGGCCTTG[-/TC]TCTACAAAAAAATAA | 50807 |
rs10580646 | snp | A/G | 0.244898 | 0.249948 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283587 | ACTCCATCACAGAAA[A/G]AAAAAAAAAAAAAAA | 50807 |
rs10597824 | in-del | -/AT | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277802 | ATGTCTTTGCCACTC[-/AT]TATTGTGTCTGTTGA | 50807 |
rs10602064 | in-del | -/AAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312292 | TAAAAAAAAAAAAAA[-/AAA]GTACCATGCCTAAAA | 50807 |
rs10657960 | in-del | -/TCA | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317043 | TTTGGTACATTATAC[-/TCA]ACCTTGAGACTCATT | 50807 |
rs10678353 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082737 | TTTTTTTTTTTTTTT[-/T]GGTAGAGACAAGGTC | 50807 |
rs10678909 | in-del | -/CC/TC/TCTCT/TCTCTCTCTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276761 | CTCTCTCTCTCTCTC[-/CC/TC/TCTCT/TCTCTCTCTT]CTCTAACAAAAAAGC | 50807 |
rs10679649 | in-del | -/T/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205608 | ATAAAATACACGGCT[-/T/TT]TTTTTTTTTTTTTTT | 50807 |
rs10689183 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205609 | TTTTTTTTTTTTTTT[-/T]AGCTTAAACTCACTT | 50807 |
rs10690482 | in-del | -/AAA | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085755 | AAAAAAAAAAAAAAA[-/AAA]GGAAAGAGGTTCAAT | 50807 |
rs10710342 | in-del | -/A | 0.409552 | 0.192466 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409262 | gtgagacggtgtctc[-/A]aaaaaaaaaacaaaa | 50807 |
rs10956511 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118348 | ATAAGGAGCACACCT[C/T]TTCACTCTCATATTC | 50807 |
rs10956512 | snp | C/G | 0.39121 | 0.2063 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188603 | GCCAGGTATGGTGGT[C/G]TACAACTGTAGTTCC | 50807 |
rs10956513 | snp | A/T | 0.365439 | 0.221752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235978 | TTCAACAACTTTTTT[A/T]AATACCACTATCCTC | 50807 |
rs10956514 | snp | A/G | 0.490836 | 0.0670685 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240512 | ATCCTCTGAAATGTC[A/G]TATATGTAAAATTAA | 50807 |
rs10956515 | snp | C/T | 0.337841 | 0.23406 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249395 | CATGATGTCCTAACA[C/T]GCCAGGCTCCTTTCT | 50807 |
rs10956516 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257317 | AATGAGCAAGCAGTT[C/T]CCCCAATATCCAATG | 50807 |
rs10956517 | snp | A/G | 0.33693 | 0.2344 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272072 | GGGGAGGCTGAGACA[A/G]GAGGATTGCTTGAGC | 50807 |
rs10956519 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321599 | TCTAACTACATAAAC[C/G]TAATAAAGACTCTGT | 50807 |
rs10956520 | snp | A/G | 0.287867 | 0.247116 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399101 | cttaaaggatgggac[A/G]tgcctttctctgtct | 50807 |
rs10956521 | snp | A/G | 0.424193 | 0.179323 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399397 | TAATTAATATCACCT[A/G]AAAAGATACCTGCAA | 50807 |
rs10956522 | snp | C/T | 0.40595 | 0.195396 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399410 | CTGAAAAGATACCTG[C/T]AAAATGAATGCCATT | 50807 |
rs10956523 | snp | A/G | 0.457969 | 0.138741 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402644 | GTGATTCCTAGCTCA[A/G]TGTGGCATCTCCATC | 50807 |
rs10956524 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402920 | ATAATCTTTTGTGGG[G/T]TTTTTTTTTTTTTAA | 50807 |
rs10956525 | snp | C/T | 0.268452 | 0.249318 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430605 | AAGTTTTAAGGAGAT[C/T]TCCCTGAGGCAGCTC | 50807 |
rs11271133 | snp | A/C | 0.46875 | 0.121031 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300188 | GAGAGAGAGAGAGAG[A/C]GAGCGAGCGAGCAGT | 50807 |
rs11285770 | in-del | -/C | 0.288646 | 0.246995 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267102 | AGTGAGACTCTGTCT[-/C]AAAACAAACAAACAA | 50807 |
rs11311647 | in-del | -/A | 0.398714 | 0.200958 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375565 | TTGGACTCTCGAGGG[-/A]AAAAAAAAAAAAGGT | 50807 |
rs11315329 | in-del | -/G | 0.388021 | 0.208447 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247232 | TCAGAGTCTGATTTT[-/G]GTTCATTCTTGTCTC | 50807 |
rs11324057 | in-del | -/T | 0.498481 | 0.027514 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176689 | ATGTCTCTCTTCCTG[-/T]TTTTTTTTTTTTTCT | 50807 |
rs11324757 | in-del | -/T | 0.405429 | 0.195811 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219197 | CAGGTCTCACATGTC[-/T]TTTTTTTTTTTAACA | 50807 |
rs11327491 | in-del | -/T | 0.463559 | 0.129972 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162318 | TTTGTTTTGTTGTTG[-/T]TTTTTTAAGAGAGGC | 50807 |
rs11340723 | in-del | -/T | 0.154993 | 0.231244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418777 | CAAAAAAAATAGGAG[-/T]TTTTTTTTTTTTAAT | 50807 |
rs11348187 | in-del | -/T | 0.497881 | 0.0324789 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317102 | AGTTTCACATCATGC[-/T]TTTTTTTTTTTTTTA | 50807 |
rs11351906 | in-del | -/A | 0.425277 | 0.178263 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381549 | CACAGTTTGAGCACC[-/A]AAAGAGAATGGAGAA | 50807 |
rs11354681 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334134 | GTTTGCTTCTGCTCC[-/T]TCTGGCAGCAGCAGA | 50807 |
rs11392401 | in-del | -/T | 0.235777 | 0.249595 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169102 | GATTTACCACCAGTA[-/T]TAAAAAAAAAAGAGT | 50807 |
rs11392655 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257786 | TTGGACTCAAGAGCA[-/C]CCCCCCCCCCATTAT | 50807 |
rs11414704 | in-del | -/TT | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082501 | CCACCACACGTGGCC[-/TT]TTTTTTTTTTTTTTT | 50807 |
rs11420981 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352213 | TTTTTTTTTTTTTTT[-/T]AAGACTACAATCTCC | 50807 |
rs11421234 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196342 | AAAAAAAAAAAAAAA[-/A]GTTGTAGGTCACACT | 50807 |
rs11435697 | in-del | -/A | 0.409382 | 0.192607 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405277 | TTATAGATGAAAAAA[-/A]TCATAACTCACAAGA | 50807 |
rs11451150 | in-del | -/A | 0.120326 | 0.21374 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417073 | CACATACACACATGC[-/A]AAAGTGCAACCCATG | 50807 |
rs11455175 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400492 | GTAACGTGGCATAGG[-/A]GAAAAAAAAAAAGGC | 50807 |
rs11552955 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227530 | CCCAAAGTGCTAGAA[C/T]TACAGGCCTGAGCCA | 50807 |
rs11557146 | snp | C/T | | | missense | ASAP1 | GRCh38.p7 | 8:130214591 | GTCAAGTTTTCTACT[C/T]TTACAAAGGAACTGT | 50807 |
rs11774131 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077528 | AAGAGTTGGTTGCTG[C/T]TGCTGCTGCTTTTTT | 50807 |
rs11774346 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368178 | TGCTCTGGCCTTAGA[G/T]GTTGAGAGGCATTAT | 50807 |
rs11774633 | snp | C/T | 0.439502 | 0.163061 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177997 | AAGAATACAGTTAAC[C/T]AGCTGCAGAGCCAAA | 50807 |
rs11774659 | snp | C/T | 0.441158 | 0.161117 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178090 | CCTCCTTAAATGTTT[C/T]AGTTGAATACAGGTA | 50807 |
rs11774686 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178073 | cATAATATTAATGCT[A/G]ACCTCCTTAAATGTT | 50807 |
rs11774690 | snp | C/G | 0.490508 | 0.0682328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178252 | TTCTGGAAGGTCCTT[C/G]CATTATTTTCGGTAT | 50807 |
rs11774947 | snp | A/C | 0.497907 | 0.0322805 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283777 | GCCTTAAAACCAGGT[A/C]TAGAAAATCAGATTT | 50807 |
rs11775172 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368774 | aagatggcaagagat[A/G]cgggagagtcgtggt | 50807 |
rs11775292 | snp | C/T | 0.498589 | 0.02652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204949 | GAATTACTTGTATAG[C/T]AAAAGTTAACCATAA | 50807 |
rs11775309 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419715 | AAGACAGGAGGGAGG[A/G]AGAGGGAGGCTGAGG | 50807 |
rs11775398 | snp | A/G | 0.262985 | 0.249663 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427521 | ATACTTGGCCTATAA[A/G]ATCCCAATTTAATCT | 50807 |
rs11775609 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209036 | TGCAATTCCCCTGTA[A/G]GCATGTGTTCTTTTT | 50807 |
rs11776078 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068723 | tcaccctgagaaggg[C/G]gactgtccaactcta | 50807 |
rs11776241 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130184778 | CTTAAAGAGAACTTA[C/G]TAGAAACTatttatt | 50807 |
rs11776262 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398135 | gacATGtttttattg[A/C]catataagatacata | 50807 |
rs11776395 | snp | C/G | 0.00943375 | 0.0680285 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215451 | aaaaattaacaatta[C/G]ctgggtgtagggccg | 50807 |
rs11776732 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437429 | TCTCAGTTAAGTCAG[C/T]ATGGTCAGTGCAAAA | 50807 |
rs11776768 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437521 | CATTCCACTGAGCCA[C/T]CCTGCATCCCCCAAG | 50807 |
rs11776863 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132993 | GAGTGGGAGAGAGAA[A/G]AGAAGTGAGTATAAG | 50807 |
rs11777289 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177052 | CATTATGATTAATAA[C/T]GGATCTGACTTACTT | 50807 |
rs11777354 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151514 | ATGGGTAGCTGGACA[C/T]AACTGGCATGACAGC | 50807 |
rs11777909 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242980 | TGAGATTTTTTCTGA[C/T]GATCATCAAACTTGG | 50807 |
rs11778072 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364802 | ACTTCCTCAGCAACA[A/C]ATAGCTCTGTTAGCA | 50807 |
rs11778323 | snp | C/T | 0.325799 | 0.238232 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414212 | TAGAAAGACCTTTCA[C/T]TGGACGAATGTTTGC | 50807 |
rs11778454 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086710 | tcaggagactgaggt[A/G]ggaagatagcttgag | 50807 |
rs11778504 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380734 | ACATGAAATTAAttt[A/C]atttttttagagaca | 50807 |
rs11778593 | snp | C/T | 0.0429648 | 0.14013 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409154 | gtagtcccagctact[C/T]gggaggctggggcag | 50807 |
rs11778712 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379454 | aaacctctcaattta[C/T]agctggttggtcaga | 50807 |
rs11778881 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278941 | TCATCCATTAGTTCA[C/T]TCAAAACAATCCTTA | 50807 |
rs11779014 | snp | A/G | 0.346811 | 0.230494 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341488 | TAAAACCTGGGACAG[A/G]AAACTGCTGACTGCC | 50807 |
rs11779191 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092800 | CACACACCACTACCA[A/G]CAAAATCAACAGAGA | 50807 |
rs11779293 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394176 | cttaaactttgacca[C/T]cggtgagctgggcgg | 50807 |
rs11779475 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130175918 | ATTATCTGTAAAATG[A/C]CAGATAATAAAGCAA | 50807 |
rs11780440 | snp | A/G | 0.00938946 | 0.0678717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081782 | CTGGGAGTCCTGACC[A/G]CAAATCAATGTGCTC | 50807 |
rs11780644 | snp | A/G | 0.328148 | 0.237472 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437665 | TGTTACACACAGGAC[A/G]AGTTTTTACAGAGGC | 50807 |
rs11781126 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395780 | caagcgattctcctg[C/T]ctcagcctcccgagg | 50807 |
rs11781178 | snp | A/G | 0.00947846 | 0.0681864 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360950 | TGGCCCATGCTAGTT[A/G]AGCTAATTAAGCTCT | 50807 |
rs11781211 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395958 | ggtgtgagccaccgc[A/G]cctggccatatttct | 50807 |
rs11781272 | snp | C/G | 0.0652144 | 0.168387 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054602 | CACACATTATATCCC[C/G]CTCCTGAGGTGGCCC | 50807 |
rs11781294 | snp | A/C | 0.113093 | 0.209181 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054682 | AGGGTTACATGAAGG[A/C]AGCAGTCTTGCATGA | 50807 |
rs11781752 | snp | A/G | 0.388964 | 0.20782 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195733 | CTTAAGGAAGCAAGT[A/G]ACTGTAATTAATATT | 50807 |
rs11781836 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247214 | TCCTTTCCCCAATGG[G/T]CCTCAGAGTCTGATT | 50807 |
rs11781851 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071059 | gagaaagCAGAGTTT[A/C]CCCAAATCATCTAAG | 50807 |
rs11781912 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247476 | TCATAACCATGTTGC[A/T]CTCCAACCCTTCAAC | 50807 |
rs11781929 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131522 | taatcccagcacttt[C/T]tggggtcgaggtggg | 50807 |
rs11782152 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156276 | CATGTATAAGCATTT[C/T]AATTTTTTACTCTTC | 50807 |
rs11782240 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397147 | TATGAGAAttttgtt[A/G]ttgttgttgttaaga | 50807 |
rs11782883 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093168 | GGAATGATAGTAATA[C/T]TCCACATACACACAA | 50807 |
rs11783764 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403673 | ttctcctccctcagc[C/T]tcccaagtagctggg | 50807 |
rs11783860 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103108 | ttacttattattaat[C/T]tgctcaggttttcta | 50807 |
rs11783940 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073295 | cttgggaggccgagg[C/T]aggagaatcgcttga | 50807 |
rs11784041 | snp | G/T | 0.460252 | 0.135255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354641 | TCATAACTTAAAAAT[G/T]GTCAAGAGTAAAATG | 50807 |
rs11784477 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379728 | ACCAGAGATGCTGGA[C/T]GCTGCCTGTGCCATT | 50807 |
rs11784539 | snp | C/T | 0.390277 | 0.206936 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400943 | tggagtgcaacagtg[C/T]gatcttggcccactg | 50807 |
rs11784613 | snp | A/T | 0.00938946 | 0.0678717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100312 | gccatttatatgtcg[A/T]gttttctttctttct | 50807 |
rs11784638 | snp | A/G | 0.426813 | 0.17674 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410227 | AGGAATAAGACCTTC[A/G]TCAAAAAACCTCACC | 50807 |
rs11784783 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395727 | gctggagtgcagtga[C/T]gtgacctcggctcac | 50807 |
rs11784842 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395939 | ccaaagtgctgggat[G/T]ataggtgtgagccac | 50807 |
rs11784889 | snp | A/T | 0.12932 | 0.218944 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396119 | CACAGACCCTGGCAC[A/T]TAGTAGGTCGTCAGA | 50807 |
rs11784953 | snp | C/T | 0.12932 | 0.218944 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396320 | ATGTATTTCCCCAGG[C/T]TTGAGTGTAGGACCT | 50807 |
rs11784988 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396463 | CCTTCCTTTATGTAT[C/T]TAACTGAAGTATAGT | 50807 |
rs11785125 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325972 | tgatgttttaagtac[C/T]atcattatccccaat | 50807 |
rs11785146 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247387 | AAAATTGAACATCAG[A/C]ATGGCCCTAAGATAT | 50807 |
rs11785172 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304993 | tcttcttcctcacac[A/G]ctctacaccttggcc | 50807 |
rs11785286 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240446 | ATAATACAAGTCTAA[A/G]TGTGCTACAAAGTTT | 50807 |
rs11785594 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411410 | CCCAGCTCCTTGCCC[C/T]TTGGTTCTGACAACC | 50807 |
rs11785806 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397168 | gttgttaagaaagag[A/T]ctagttctgttgccc | 50807 |
rs11786205 | snp | A/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262571 | GTAGCCTTTGAATGT[A/T]AACTGGAATTCCTAG | 50807 |
rs11786359 | snp | A/C | 0.323197 | 0.239044 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419150 | AAAAACCGAGGCTTC[A/C]GTCAAACAGATGGTC | 50807 |
rs11786705 | snp | A/G | 0.339656 | 0.233371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341845 | ATTAACAAATAAGAG[A/G]TAAAAGAGCAGCAAG | 50807 |
rs11787251 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149142 | ttacaggcatgagcc[A/G]ccgcgcctggccTGA | 50807 |
rs11787373 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325332 | GTAATACAGATTTCT[A/C]GCACTGAGGCCAACT | 50807 |
rs11984555 | snp | A/T | 0.498982 | 0.0225409 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364066 | GGTAATAATAATAAT[A/T]AAAAAAAGCCAATTC | 50807 |
rs11984909 | snp | A/G | 0.431029 | 0.17242 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396088 | TTTTTGTTTCCCTTG[A/G]TATCCTGGCAGCTTG | 50807 |
rs11986237 | snp | C/T | 0.143959 | 0.226396 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083949 | AGGCATGCGCCACCA[C/T]GTCTGGCTAATTTTT | 50807 |
rs11988507 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387437 | cttacttgggaggct[G/T]aggcaggagaatcac | 50807 |
rs11988989 | snp | A/G | 0.135143 | 0.222054 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091846 | ATGTCATATATACCC[A/G]AGTCAGCACCCAGCA | 50807 |
rs11991819 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195325 | gggaactgcttgagc[C/G]catgagttcaagaac | 50807 |
rs11992217 | snp | G/T | 0.431473 | 0.171952 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387290 | CCTGTAATCCCGGCA[G/T]TTGGGGAGGCCGAGG | 50807 |
rs11992885 | snp | C/T | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402318 | GATGCGACAGACAGA[C/T]AGACAGACACCTGCA | 50807 |
rs11992932 | snp | G/T | 0.409041 | 0.192888 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402338 | AGACACCTGCAGCTG[G/T]GTGCCCACGAGAAAG | 50807 |
rs11992957 | snp | C/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402386 | CAAAGGAAACCAGTT[C/G]CAGGAAGAAGGCAGA | 50807 |
rs11993714 | snp | C/T | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402763 | CTAAAGATCTCTCCA[C/T]TTATCTCTCCCCACC | 50807 |
rs11993716 | snp | A/G | 0.274393 | 0.248807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161880 | ATCACAGCTCACTGC[A/G]GCCTGAACCTCCCAA | 50807 |
rs11993741 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402666 | ATCTCCATCCAGGGC[A/G]AAAAACCGAGAGACA | 50807 |
rs11995309 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295515 | AACAGGGATACGGGA[C/T]AATAATACCTAGTTA | 50807 |
rs11995727 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059924 | ctctaccaaaaatat[A/T]aaaaaaaagccaggc | 50807 |
rs11996310 | snp | A/T | 0.164546 | 0.234942 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387588 | TTTTTAACTACTTGT[A/T]TACATATATCAAAAT | 50807 |
rs11997462 | snp | C/T | 0.40853 | 0.193309 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402597 | GGATATAAAAATAAA[C/T]TGAGCCAAGGGACCT | 50807 |
rs12056438 | snp | A/G | 0.489722 | 0.0709447 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144756 | AGTAATTCATTCTAG[A/G]GTAGATGGCTGAATT | 50807 |
rs12056781 | snp | C/T | 0.249038 | 0.249998 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434414 | TGCGTATTTCAGGTT[C/T]GTCGTATATAAAATG | 50807 |
rs12155934 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360490 | GCTGTACTGAACCTG[C/T]ACTGTGCCTCCAGCG | 50807 |
rs12155939 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267127 | aaacaaacaaacaaa[A/C]aaaaaacaaaacaaa | 50807 |
rs12334490 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115118 | tttggtcaaatacta[A/G]tctagatgttgctgt | 50807 |
rs12541083 | snp | A/C | 0.33303 | 0.235809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313223 | AATCCCTAAAGCCTG[A/C]AGATAATTTCTAAGC | 50807 |
rs12541938 | snp | A/G | 0.321053 | 0.23969 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068267 | tcaggacttgaggct[A/G]gactaagctcagatg | 50807 |
rs12542329 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168791 | CCCCTCCCTGCTCCT[C/G]TTATGGCCCCAGAAG | 50807 |
rs12542411 | snp | C/T | 0.322245 | 0.239334 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109064 | ATAGGCGTAAGCCAC[C/T]GCACCCGGTCCAAGA | 50807 |
rs12543817 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107510 | Ctttttttttttttt[A/T]aaaaaatgtatgtat | 50807 |
rs12544998 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168770 | TGGAACTGATGGCTG[A/T]ATACTCCCCTCCCTG | 50807 |
rs12545910 | snp | A/G | 0.340784 | 0.232934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170116 | TTGAGCATGAGGACT[A/G]TCTCATCTCCCTATC | 50807 |
rs12546088 | snp | A/C | 0.337386 | 0.23423 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066672 | TTTAGAATAGTTCCT[A/C]TACCTACCAACTACA | 50807 |
rs12546128 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070155 | cattctcctgcctca[A/G]cctcctgagtagctg | 50807 |
rs12546206 | snp | A/G | 0.490836 | 0.0670685 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154802 | AACATACTGTATTCA[A/G]AATGCTAGCCTTGCT | 50807 |
rs12546603 | snp | A/G | 0.325091 | 0.238456 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077673 | GCCTCAGCTAACTGC[A/G]TTTAAAAGAAAAGAA | 50807 |
rs12547397 | snp | A/G | 0.334182 | 0.235401 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257069 | TTTATAAAAACTAAT[A/G]TAACTGTTTTCCAAA | 50807 |
rs12547540 | snp | C/T | 0.35207 | 0.228214 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188499 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA | 50807 |
rs12548888 | snp | A/G | 0.470811 | 0.117228 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164452 | AAAAATTAGCCAGGC[A/G]TGGTGGTACATGCCT | 50807 |
rs12549794 | snp | C/T | 0.471768 | 0.115407 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202001 | CGTACTAGGGTGACA[C/T]AGTAATGTCTCATAG | 50807 |
rs12550192 | snp | A/T | 0.130008 | 0.219321 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397721 | GGAACTTTTCCCCCA[A/T]CAAAGGGGTTGGTTG | 50807 |
rs12550365 | snp | A/T | 0.459914 | 0.13578 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123800 | GCCCGGCTAATTTTT[A/T]AAAAATTTTTAATAG | 50807 |
rs12550366 | snp | A/T | 0.468949 | 0.12067 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123801 | CCCGGCTAATTTTTA[A/T]AAAATTTTTAATAGA | 50807 |
rs12675390 | snp | C/T | 0.394354 | 0.204112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205446 | ATATATACACTAGGA[C/T]ACCTGTTTATTGGAT | 50807 |
rs12675543 | snp | C/T | 0.324145 | 0.238752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105262 | TAGCAACCATTTACA[C/T]AGCATTTACATTGTA | 50807 |
rs12675936 | snp | C/T | 0.124837 | 0.216412 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120346 | AAAAATTAAATCGCT[C/T]GATTCAAGTCTGAGA | 50807 |
rs12676014 | snp | A/T | 0.123105 | 0.215401 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232845 | TTGTATCACTTAAGC[A/T]TTGTGAGAAAACAAG | 50807 |
rs12676156 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407276 | CCTTCTGAGAGACTG[C/T]GGAGAGCACATCTCA | 50807 |
rs12676536 | snp | C/T | 0.268452 | 0.249318 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121547 | agcacactgggaggc[C/T]gaggtgggtgaatca | 50807 |
rs12676577 | snp | G/T | 0.122064 | 0.214785 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082530 | TTTTTAAGAGACAAG[G/T]TCTTGCTCTGTCACC | 50807 |
rs12676836 | snp | C/T | 0.337614 | 0.234145 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212730 | GACAAACAAATGTAT[C/T]AGGTGAGCAAACGCA | 50807 |
rs12676977 | snp | C/T | 0.281049 | 0.248064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121676 | gtaatcccagctatt[C/T]gggaggctgcgacag | 50807 |
rs12677139 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092386 | atcccctgcactgta[A/G]aaagctgaggtggga | 50807 |
rs12677193 | snp | C/T | 0.493658 | 0.0559517 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107907 | AAGAGGAGAAGGTGA[C/T]GCTGGAAAGGCTTCT | 50807 |
rs12678030 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399714 | CTACTTTATGTAAAA[C/T]ACTTTACATTTTTTC | 50807 |
rs12678062 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399888 | acaatggcgcaatct[C/T]ggctcaccaaaacct | 50807 |
rs12678316 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148879 | tggctctgtcgccca[A/G]gctggagtgcagtgg | 50807 |
rs12678808 | snp | C/G | 0.327914 | 0.237549 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395988 | TGTTGTTTTAAGCCA[C/G]CAAGTTTGTGGTACT | 50807 |
rs12679149 | snp | A/T | 0.389903 | 0.207189 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121763 | cactccagcctaggc[A/T]atgagagtgaaattc | 50807 |
rs12679213 | snp | C/G | 0.00938946 | 0.0678717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371749 | aaacagaaaaggctt[C/G]ggctcctgataacca | 50807 |
rs12679283 | snp | A/G | 0.342358 | 0.232314 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308717 | CAACTCCCTCAGTAC[A/G]TATCAACTAATAAGA | 50807 |
rs12679327 | snp | C/G/T | 0.00938946 | 0.0678717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331734 | GTATTTTATTAGCAA[C/G/T]ATTAAAAATACAAGC | 50807 |
rs12680178 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399587 | TCAGGTTGGCCTCTC[C/T]GCCTCCAGCCTCTCA | 50807 |
rs12680697 | snp | A/G | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399541 | TTTACCCTGGAAGGC[A/G]GTATCATGTCTCGAT | 50807 |
rs12680942 | snp | A/G | 0.464629 | 0.128197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251787 | ATGCAAGTAATTTCA[A/G]TTGCACTGATAAGTT | 50807 |
rs12681050 | snp | C/T | 0.00938946 | 0.0678717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229543 | GTGGTCCTTAACAGT[C/T]ATTAATCTGAATCTT | 50807 |
rs12681590 | snp | C/T | 0.161924 | 0.233971 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331849 | AAGTGGGGAGAATGA[C/T]CAGAATCCACAAAAG | 50807 |
rs12681664 | snp | A/G | 0.243633 | 0.249919 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406205 | CTGCCTAAAGACAGA[A/G]CAAAGAACAAAAGAA | 50807 |
rs12681954 | snp | C/T | 0.333491 | 0.235646 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236089 | AAGGACGAAAGCCCA[C/T]ATCTGTCCAACTTCA | 50807 |
rs12681955 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236112 | CAACTTCACGGCCTG[C/T]GCTCTTTCTATTATA | 50807 |
rs12682258 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093686 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGCTAAGAA | 50807 |
rs12707941 | snp | G/T | 0.493523 | 0.0565391 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432550 | TAGTTACAAATAACA[G/T]AAAACTCCCATCAGA | 50807 |
rs13248539 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400719 | tggcgtgaagccggg[A/T]ggcggagcttgcagt | 50807 |
rs13249018 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121449 | gccaagtatcctctg[A/G]gggcaaagtcaccct | 50807 |
rs13249894 | snp | C/T | 0.418974 | 0.184249 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407632 | CAGAATTCATTACCA[C/T]CAAGCATCAGATTTG | 50807 |
rs13250093 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085738 | AGACGTTGTCTTTAA[A/G]AAAAAAAAAAAAAAA | 50807 |
rs13250469 | snp | C/T | 0.359998 | 0.2245 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129821 | TGTGATGCAGAAAAC[C/T]GAACATTTCAAAACC | 50807 |
rs13250580 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400606 | tcctggctaacacgg[G/T]gaaacccgtctctac | 50807 |
rs13251129 | snp | C/G | 0.164219 | 0.234823 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086248 | GTGAATCCTGGCCCC[C/G]ACGTACTAGCTGTGA | 50807 |
rs13251433 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130440156 | tgctgctgtccagtt[C/T]taagccaccatcctc | 50807 |
rs13252244 | snp | A/C | 0.106633 | 0.204807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228743 | AAATAATGAAAAAAA[A/C]CAAAAAAACCTTTAA | 50807 |
rs13253189 | snp | A/G | 0.25634 | 0.24992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133757 | TTTCCACTATATCAC[A/G]CTCCCTTTTATTGAC | 50807 |
rs13254924 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435406 | TAGGCACTAGGGATT[A/C]CAGAAATGATCAGGG | 50807 |
rs13255178 | snp | C/T | 0.243633 | 0.249919 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405349 | ACTAAGATCCTGACC[C/T]GGGTGGTCTAAAAAA | 50807 |
rs13256967 | snp | A/G | 0.266546 | 0.249452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128999 | tctggggagagaccc[A/G]tgtaggaggtgattg | 50807 |
rs13258946 | snp | A/C | 0.492823 | 0.0594727 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344146 | ggaaactacgggata[A/C]accaccactttcttt | 50807 |
rs13259204 | snp | C/T | 0.0186899 | 0.0948454 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209775 | ttgaactaactggca[C/T]tgtttttttagtgga | 50807 |
rs13259736 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070919 | ggagagagaggggga[C/G]agagagggggagaga | 50807 |
rs13260346 | snp | C/G | 0.314057 | 0.241654 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387842 | ATATTTACTGAACAT[C/G]TATGTACCAGACTCT | 50807 |
rs13265869 | snp | C/T | 0.496753 | 0.0401586 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340893 | AGGCTGACCAATCAT[C/T]GCGATGAATGACAAA | 50807 |
rs13267150 | snp | A/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172435 | ACTACTGAAATAAAC[A/T]TTTTTTAAAAATAAG | 50807 |
rs13269464 | snp | C/T | 0.470618 | 0.117591 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087736 | ACAAGTTTGATTCCA[C/T]ATTTAATGTTAGGCA | 50807 |
rs13269735 | snp | C/T | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131635 | AAAAAAAAAAAGAAA[C/T]GAAAATTAGCTGGGC | 50807 |
rs13269931 | snp | C/T | 0.261332 | 0.249743 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250321 | CAAAAAACTAGTAAA[C/T]GGAAAAATCAGGATT | 50807 |
rs13271077 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381682 | tactcccatgactta[A/G]tctaaaggccttata | 50807 |
rs13272051 | snp | A/G | 0.46845 | 0.121572 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389480 | GTATTACAAAACCAA[A/G]TCTTATTTTGCATTT | 50807 |
rs13272223 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141390 | GCAGGCCCTCGGAGA[C/G]CTCCCTGCTCACTCC | 50807 |
rs13272567 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428163 | CAAACGTCACTTCAC[A/C]TCTTGAGGAACTGTC | 50807 |
rs13272817 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428201 | AGTGTCCATCTCACT[A/C]TCTAGACTGGGAATA | 50807 |
rs13272819 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428203 | TGTCCATCTCACTCT[A/C]TAGACTGGGAATATT | 50807 |
rs13272849 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420823 | acttgaactcgggag[C/G]cagaggttgcagtga | 50807 |
rs13273116 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428327 | TCATGCCAGTGCTCG[A/C]TAAATTAAAGCCACA | 50807 |
rs13274091 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130429948 | GATGATACATCCCAG[A/T]GCCTGGGCAACGTGC | 50807 |
rs13274832 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429949 | ATGATACATCCCAGA[A/G]CCTGGGCAACGTGCC | 50807 |
rs13275147 | snp | G/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399950 | TCAGCCTCCCAAGTA[G/T]CTGGGATTACAGGCA | 50807 |
rs13275883 | snp | A/C | 0.419296 | 0.183954 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370326 | aaacaaacaaacaaa[A/C]aaaacagagagcagc | 50807 |
rs13275897 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123595 | GCTCTGGAaaacaaa[C/T]aaacaaacaaacaaa | 50807 |
rs13276034 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188741 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 50807 |
rs13276168 | snp | G/T | 0.409212 | 0.192748 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407487 | CATCTGTACATAGAC[G/T]CTCAATAAATATCTG | 50807 |
rs13276180 | snp | A/C/G | 2.36992e-05 | 0.00344224 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358195 | GTGAGTCACGGCGCA[A/C/G]GCTcccggggccgcg | 50807 |
rs13278110 | snp | C/T | 0.349671 | 0.229272 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085159 | GGGGGAAATTGTTAT[C/T]AGGTATTAATTCAAG | 50807 |
rs13278799 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276730 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 50807 |
rs13280092 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221452 | agtctgcataaataa[A/C]ccttgttaaaataat | 50807 |
rs13281273 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169839 | agctagtaagcagca[A/G]agctggtggaattca | 50807 |
rs13438852 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082742 | tttttttttttggta[A/G]agacaaggtctcact | 50807 |
rs13439019 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350913 | CTCATAGGCAAATCA[A/G]GTTGGGTCAACAGTC | 50807 |
rs13439267 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369680 | atgaaatgccacttt[A/G]cacccactaggatgg | 50807 |
rs13439329 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130082203 | ACTGGCATTACTAGA[A/G]GAACCAAAGGCTTTC | 50807 |
rs13439609 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270452 | CTGTATGTAAAAGTA[C/T]AAAGAAATAACTTCC | 50807 |
rs16893265 | snp | C/G | 0.227074 | 0.248947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191987 | AACTAATTTTACACA[C/G]CGGAAGGTTTCCCAA | 50807 |
rs16893271 | snp | A/G | 0.340784 | 0.232934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268143 | CAGAAATGATTTAGT[A/G]AATTAAGGAACATCT | 50807 |
rs16893272 | snp | A/T | 0.0513262 | 0.151752 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295931 | AATTTATGATATCCC[A/T]TCATCTTTGCCTCTC | 50807 |
rs16904197 | snp | C/T | 0.338296 | 0.233889 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064019 | GTCAGGGAAGGCCAC[C/T]CTGATATGGCAAGAG | 50807 |
rs16904198 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065835 | TTTCATAATCGTGTA[A/C]TAGCCTCACTGTTCT | 50807 |
rs16904199 | snp | A/G | 0.335788 | 0.23482 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066304 | TCACAGGCTTGTACT[A/G]CTGGTTTCCACTGGG | 50807 |
rs16904200 | snp | C/T | 0.0509478 | 0.151255 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082911 | GTCTTCAGGGCTAGA[C/T]ATCAAATCTTATACT | 50807 |
rs16904201 | snp | A/G | 0.171704 | 0.237423 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084093 | CCACTGCGCCAGGCC[A/G]ATAACACCACTTTTT | 50807 |
rs16904202 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091824 | CCCTTAAGAGACAGG[C/T]AGAATCATGTCATAT | 50807 |
rs16904203 | snp | C/T | 0.138886 | 0.22395 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094848 | GATAATAGACAATGG[C/T]GAGGTTCTCTAGCAA | 50807 |
rs16904204 | snp | C/T | 0.335101 | 0.23507 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107007 | ACTGAATGCTCACTA[C/T]GTGCCAGTCATTTCA | 50807 |
rs16904205 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108296 | ATATAATGCCTGATT[C/G]TAGAGGCCTGGCTTC | 50807 |
rs16904206 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121869 | TCCTGTTTAAAACCT[C/T]TCAATCACACTTACA | 50807 |
rs16904207 | snp | A/T | 0.125182 | 0.216612 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174516 | ACCAGTCACCGCACT[A/T]TTATACACAATTCAT | 50807 |
rs16904208 | snp | A/G | 0.33693 | 0.2344 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176472 | TAACATGGTTCTACT[A/G]CTTGATGTCTCAGAA | 50807 |
rs16904209 | snp | C/T | 0.239614 | 0.249784 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177134 | TCCCAGAACTGGGCA[C/T]AGTAGCTGATCTTTG | 50807 |
rs16904210 | snp | C/T | 0.239614 | 0.249784 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177255 | CATTACTAGCGAAGG[C/T]TAATATATGTATACT | 50807 |
rs16904211 | snp | A/C | 0.133093 | 0.220981 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177704 | TTTACTTTGAAAAAA[A/C]GTTATCATCAAATTT | 50807 |
rs16904212 | snp | C/T | 0.339656 | 0.233371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178305 | CTTTACTAATACAGA[C/T]TTTACTTTTCTGGTA | 50807 |
rs16904213 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183854 | ATTAGATTTAAAACT[A/G]AAGAGAGTCAAACGC | 50807 |
rs16904214 | snp | C/G | 0.237882 | 0.249706 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187052 | CATGCAACCACTTTA[C/G]GTCAGTGTACCCAAC | 50807 |
rs16904215 | snp | C/T | 0.244205 | 0.249933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191509 | GATGAATAAACACTG[C/T]TCCTACCTGTGGAGA | 50807 |
rs16904216 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207293 | TTAATGAGAGGAAGG[A/G]TAAGTTTAGAGAGAT | 50807 |
rs16904217 | snp | A/G | 0.079617 | 0.182947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211135 | AGCCTCTCGAATCCT[A/G]TGTTACAAGGTAGAA | 50807 |
rs16904218 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211872 | GCTTAACGTTTCTGG[C/T]CTTCACTAGCCTAAG | 50807 |
rs16904219 | snp | C/T | 0.342358 | 0.232314 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213379 | CAGAGAAAAAGAATA[C/T]TGTAACTGGCCAAAT | 50807 |
rs16904220 | snp | A/G | 0.125874 | 0.217008 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222942 | AGATGCCAAGTGATT[A/G]AGAAACCTGAAAATC | 50807 |
rs16904221 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223890 | CATGAACGAAGAAAA[A/G]TCTTCCAGAGGATAG | 50807 |
rs16904223 | snp | C/T | 0.34146 | 0.23267 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232621 | CATGGAGACAATTTG[C/T]TTAAAAAAAAAAAAC | 50807 |
rs16904224 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237221 | AGTGTGTGAAATGGA[C/T]AGCATTTTAGTCAGT | 50807 |
rs16904225 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237902 | TGGTCTGCTTGGGAA[C/T]CCCTAGATGATATGT | 50807 |
rs16904226 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240448 | AATACAAGTCTAAGT[A/G]TGCTACAAAGTTTTA | 50807 |
rs16904227 | snp | C/G | 0.240478 | 0.249819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244185 | AGCACTCAGTGGAAG[C/G]TGACTGAATGAACAA | 50807 |
rs16904228 | snp | C/T | 0.151001 | 0.229563 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259732 | ATGGACAGGAAGGGG[C/T]GACAGTGTGTGCAAT | 50807 |
rs16904229 | snp | C/T | 0.234692 | 0.249531 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259932 | AGTCATAGGCAGCAC[C/T]GAAAATTATTTTAAA | 50807 |
rs16904230 | snp | G/T | 0.233527 | 0.249457 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264590 | ATCTAAGCTTTTTTT[G/T]GAACTATAACTGTAT | 50807 |
rs16904231 | snp | C/T | 0.353803 | 0.227431 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269353 | CAAGTAAAATAGCCA[C/T]TCTGTGACCTGACTG | 50807 |
rs16904232 | snp | C/T | 0.232067 | 0.249356 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274665 | TATTTCATTCAAGTC[C/T]GAGTGATCAACAGAA | 50807 |
rs16904233 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274811 | ACATAAAGCCTTCCT[C/G]AATACCACCAGTACA | 50807 |
rs16904234 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275961 | GGTACTGATAATGAC[C/T]GGACTTCATCAGCGG | 50807 |
rs16904235 | snp | G/T | 0.227074 | 0.248947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284237 | TAAAACCTGGAAATT[G/T]AGTAATAATGATCCA | 50807 |
rs16904236 | snp | A/C | 0.237593 | 0.249692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284305 | GAAAACTGGACAAAC[A/C]ACCATTCTAGACAGT | 50807 |
rs16904237 | snp | C/T | 0.232943 | 0.249417 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286739 | AAGATTCACAGCATC[C/T]GACATGTTTACTGAG | 50807 |
rs16904238 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288700 | AGAAGATGGCATCTG[G/T]ACTATGGTAAAACCA | 50807 |
rs16904239 | snp | A/G | 0.333722 | 0.235565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291632 | TGATAAGTTTGACGA[A/G]TGAGTGAGAAAGTAA | 50807 |
rs16904240 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294757 | GTAAAGTCAACAAAA[A/G]GCCAATTCTAGCAGC | 50807 |
rs16904241 | snp | A/G | 0.341685 | 0.232581 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297608 | ACTATCTCCCATCAC[A/G]ATAAAACCCCCAGAA | 50807 |
rs16904242 | snp | C/G | 0.33303 | 0.235809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302823 | CAATCACTTCTAAGG[C/G]GAGAAAACTATGAAG | 50807 |
rs16904243 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305727 | ATTTTATAAATCGAG[A/G]AAACTAAAGACCAGA | 50807 |
rs16904244 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308425 | GTATGTATGTCTGTA[C/T]ACAAAAATAATTCAG | 50807 |
rs16904245 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308557 | ATAGTCAAATTAACA[C/T]TAGCATCAAGGAAGA | 50807 |
rs16904246 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309317 | GGTACACAATTTCCT[A/G]TAAAACAACAGAGGA | 50807 |
rs16904247 | snp | C/G | 0.231189 | 0.249291 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317219 | TTCTTACATAAAACT[C/G]GTACCTAAGCAAGTG | 50807 |
rs16904248 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319233 | TATGTTACTGTTGCA[C/T]TGGATCACATAGCCA | 50807 |
rs16904249 | snp | A/G | 0.340559 | 0.233022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323417 | GTAACCAACACTATC[A/G]GACAAGGGAAAGGCA | 50807 |
rs16904250 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327263 | TCTTCCAATGGCTCC[A/G]CTCAAATAAGTCACT | 50807 |
rs16904251 | snp | C/T | 0.23031 | 0.249223 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345969 | CAAGAAATTTAGTAA[C/T]TGTGGGTTTTTCCAA | 50807 |
rs16904252 | snp | A/G | 0.200182 | 0.244986 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347398 | ACTAACATCTTCCAA[A/G]CGTCACTGAGTGCCA | 50807 |
rs16904253 | snp | A/T | 0.251859 | 0.249993 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350392 | CCTCTCAAAGCAATG[A/T]GGACTAAACTAGATC | 50807 |
rs16904254 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361407 | GAGATGCAAAGAAGA[A/G]AGATTATTACAACAA | 50807 |
rs16904255 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364599 | TTGGGGTATATGTGC[A/G]TGTGTTTTCCTTCTG | 50807 |
rs16904256 | snp | C/T | 0.242488 | 0.249887 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371897 | TAATCCTAATTTATA[C/T]AATGGGCCCATGAAA | 50807 |
rs16904257 | snp | A/G | 0.227664 | 0.249 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375180 | AGGCCAGTGTCAGGG[A/G]TGGTTTATGGTTATT | 50807 |
rs16904258 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376098 | ATGTGGGCTCCCAGA[G/T]GCACATACTACAGTA | 50807 |
rs16904259 | snp | C/T | 0.34303 | 0.232046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378772 | TGCCCTGCAGATGTC[C/T]GTCAAATGCATATTA | 50807 |
rs16904260 | snp | C/T | 0.287085 | 0.247234 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387722 | ATATATATATGAAAA[C/T]TGTCTAGTCCATGAA | 50807 |
rs16904261 | snp | A/G | 0.240478 | 0.249819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391742 | AGGTCATTTCAGTCC[A/G]ATACAGTAAATGTAA | 50807 |
rs16904262 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405297 | AATCATAACTCACAA[A/G]ATATGAAATAACGTG | 50807 |
rs16904263 | snp | A/G | 0.285257 | 0.247501 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405783 | CCGTACCTCACCCAC[A/G]GCACTTGGAGACCCA | 50807 |
rs16904264 | snp | A/T | 0.269538 | 0.249235 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407561 | CTGTACAACCTCTCA[A/T]TTCCCGCTGCCACCA | 50807 |
rs16904265 | snp | C/G | 0.0894459 | 0.191631 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409354 | GGATTTTGTACTAAT[C/G]GCTAGGTCTTTCAGT | 50807 |
rs16904266 | snp | C/T | 0.0741063 | 0.177655 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409424 | CCAACCCTGATCAGC[C/T]CTGATTTAGGCATCT | 50807 |
rs16904267 | snp | C/T | 0.42666 | 0.176893 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409870 | CCTACTCTGAGTATA[C/T]TGCAGGCACTGGGCC | 50807 |
rs16904268 | snp | C/T | 0.418814 | 0.184396 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410094 | GGCTACAGCTTCCCA[C/T]AGTGAGAATTATCTT | 50807 |
rs17195950 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065946 | GCTAGATCCAGTTCC[C/T]TCTTGGGCCGTTTTC | 50807 |
rs17196525 | snp | C/T | 0.347473 | 0.230215 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111707 | CTCCACTCCACATTA[C/T]AAAAAGTACAGGTTC | 50807 |
rs17209339 | snp | C/T | 0.349013 | 0.229557 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112968 | GGTTCCTGCATTCCC[C/T]TTGGAAATATCCCTT | 50807 |
rs17210536 | snp | C/T | 0.297636 | 0.24542 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205544 | TACAATGAAACAGTA[C/T]GCAGCCTGTTAGAGC | 50807 |
rs17211546 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244167 | TGGTATCAGACCTAT[G/T]AGAGCACTCAGTGGA | 50807 |
rs17211799 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247993 | TGTGAAAGCTTCCAG[A/G]TGCCCTTTAAAATAC | 50807 |
rs17212137 | snp | G/T | 0.49975 | 0.0111793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259878 | GCTCATGAGGATAAA[G/T]AAATACTAAGGCTTT | 50807 |
rs17212453 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274594 | TCTGCCTCTCTTCTC[A/G]CTATCGCATTCATTG | 50807 |
rs17213208 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130294895 | AAATTAACATGTCTG[C/G]AAGTAAAAAAGATGA | 50807 |
rs17215817 | snp | A/G | 0.445064 | 0.156365 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407414 | CCCTCTGTGTGAATG[A/G]GCACTGTCTGCAGTG | 50807 |
rs17282526 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195697 | GGAGGCCGAGGTCTA[C/T]CTTTCATTATGCAAA | 50807 |
rs17282889 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208965 | AAGGACTAGAAAGAT[A/G]AACTCCAAGTGTCAA | 50807 |
rs17284300 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258579 | TTCAGGCTCTACCTC[A/G]GAAGGGCTCTGTGAG | 50807 |
rs17284725 | snp | A/T | 0.48679 | 0.0801892 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270478 | CTTCCCTCATTTAAA[A/T]GGTTAATTGGATAAC | 50807 |
rs17285138 | snp | A/T | 0.464629 | 0.128197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285450 | TATCACTAGAAAAAA[A/T]TTTATGGTCTAAATA | 50807 |
rs17286363 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320710 | GAAGTATCATTCCTC[C/T]CTAGTATCACATTAA | 50807 |
rs17287702 | snp | C/T | 0.240765 | 0.249829 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384315 | CCTTTTCAGATGCAA[C/T]ATCAAAGCTGTCATT | 50807 |
rs28380096 | snp | A/C | 0.19334 | 0.243495 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087668 | CAGAGTGGTGGTGTG[A/C]ACAGGTGGCCTAAAA | 50807 |
rs28396295 | snp | G/T | 0.498813 | 0.0243321 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383466 | AGAGCCCAGAGGATC[G/T]ACTATGAACCAGGCA | 50807 |
rs28407848 | snp | A/G | 0.349013 | 0.229557 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109028 | GATCCGGCCACCTCG[A/G]TCTCCCAAAGTGTTG | 50807 |
rs28413707 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170066 | TTTCTCAAAACACTA[C/T]CTGTTTTGCTGTCTC | 50807 |
rs28428574 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251735 | AAGAACAGAGGGACA[A/C]AAAACATTAACACAA | 50807 |
rs28439118 | snp | C/G | 0.128208 | 0.218327 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390942 | TATATATCCCCCGCC[C/G]CCCCAAAATTGAAAG | 50807 |
rs28445973 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374408 | GGACCAGTGGCTCAC[A/C]CCTGTAATTCCAGCA | 50807 |
rs28484664 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256739 | TGAATATACACATTC[A/T]TATATATATATATAT | 50807 |
rs28488217 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087655 | CTGGTGGGTACAACA[C/G]AGTGGTGGTGTGAAC | 50807 |
rs28491737 | snp | G/T | 0.136166 | 0.22258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195328 | AACTGCTTGAGCCCA[G/T]GAGTTCAAGAACAGC | 50807 |
rs28495072 | snp | C/G | 0.388964 | 0.20782 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180659 | TCTAATAATCAAACA[C/G]AGTCTGCCTTTAAGC | 50807 |
rs28545757 | snp | A/G | 0.316 | 0.241131 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382179 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 50807 |
rs28559741 | snp | A/T | 0.408017 | 0.193729 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391444 | AGTAATTTTTATGTT[A/T]TGCATACTTCACCAC | 50807 |
rs28562521 | snp | C/T | 0.408871 | 0.193029 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410893 | TGAGACAGAGTCTTG[C/T]TCTGTCGCCCAGGCT | 50807 |
rs28572338 | snp | C/T | 0.081446 | 0.184634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141637 | ATGGCAGCCTTGACC[C/T]CCCAGGCGAAGTGAT | 50807 |
rs28584026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296793 | TAAGCTACTTTCCAA[A/G]CAGGTAAAATTTGCT | 50807 |
rs28587625 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392464 | AACAATAACAATTAG[C/T]ATTTAGTAAGCACCT | 50807 |
rs28620907 | snp | G/T | 0.141934 | 0.225437 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116163 | AGGCCCAACTGGTGG[G/T]CCTGGAACCTGGCAC | 50807 |
rs28655885 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083941 | AGGATTACAGGCATG[C/T]GCCACCACGTCTGGC | 50807 |
rs28666821 | snp | A/G | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086743 | TGTGAGGTGGAGGCT[A/G]CAGTGAGCTATGATC | 50807 |
rs28668341 | snp | C/G | 0.468148 | 0.122112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390939 | GGGTATATATCCCCC[C/G]CCCCCCCAAAATTGA | 50807 |
rs28707621 | snp | C/T | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404014 | CAGAGAAACTCTGCA[C/T]CTTCAGATTAGATCA | 50807 |
rs28716119 | snp | C/T | 0.40853 | 0.193309 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404063 | TTAATTATGTTTCAA[C/T]GTGAAGACTGATTAA | 50807 |
rs28736405 | snp | C/T | 0.167484 | 0.23599 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136692 | ACTCACAGTCAAGCA[C/T]TGGTTTAGTTCAATG | 50807 |
rs28736860 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309008 | AAATTTGCCTGATGC[G/T]CCACACCACAAATGA | 50807 |
rs28752214 | snp | C/T | 0.359364 | 0.22481 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099123 | TCTGGAAGTGATCCT[C/T]CTACCTCAGTCTGCC | 50807 |
rs28759724 | snp | C/T | 0.246769 | 0.249979 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068659 | AGGAGGCTATTCCTG[C/T]GGTAACTGGCAGCTT | 50807 |
rs28857237 | snp | C/T | 0.138886 | 0.22395 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175063 | CCTACTGGCAATGCA[C/T]AGGTTGCAATCTTCC | 50807 |
rs33919419 | in-del | -/GACA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372969 | GCATATACACACACA[-/GACA]TACACACATACGCAC | 50807 |
rs33928192 | in-del | -/T | 0.181978 | 0.240568 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372335 | CAAAGACTTCTTTGC[-/T]TTTAAAATCAATGTT | 50807 |
rs33952386 | in-del | -/T | 0.411074 | 0.191194 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356089 | TCTCATAAAAAAAAA[-/T]ATTTGCTTTTAAATT | 50807 |
rs34003529 | snp | A/C | 0.419296 | 0.183954 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410481 | TAGCCACGCAATCCA[A/C]TCCTCATGCCAGCAG | 50807 |
rs34006260 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376903 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 50807 |
rs34012319 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087891 | CAGCTCACATCTTCT[C/G]TGAAGACTAGAAAAA | 50807 |
rs34014736 | snp | C/T | 0.103438 | 0.202533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134598 | TTACACAAGGTCACA[C/T]GGCAATAAAACAGCT | 50807 |
rs34019017 | snp | C/T | 0.409721 | 0.192325 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410606 | GGAGCCTAGGGTCTG[C/T]TGTGCTGCCCATTGT | 50807 |
rs34033236 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212369 | GGGGAGTGGGTGTGG[-/A]AAAAGGGCTGTAGCT | 50807 |
rs34038220 | in-del | -/T | 0.400325 | 0.199756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170193 | ATTTTAAGGAATATC[-/T]TTTTTTTTTTTGAGA | 50807 |
rs34043344 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350250 | GTACTGGGGAGGACT[-/C]CCCAGACTGTGAATT | 50807 |
rs34048790 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130418244 | TCACATACAATTAAT[-/G]CACAATTTAAAGTAT | 50807 |
rs34054368 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063994 | GAGAGTGACCACCAA[-/G]GAGGGTGTGGTCAGG | 50807 |
rs34065178 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130185028 | GACCACAGAAAATGT[-/G]CCAGCCTTCTCCATT | 50807 |
rs34074098 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130251815 | TTTAAAATTCCACAT[-/G]GGAACAATAATAAAA | 50807 |
rs34077610 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344226 | AAATTTGAAATATGT[-/C]CCATGAATTTCAACA | 50807 |
rs34077950 | in-del | -/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084643 | GGAGTTGGAAATGGG[-/G]TTCAAATCTCACTTC | 50807 |
rs34081670 | in-del | -/T | 0.372592 | 0.217879 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183262 | CAGAAAGGTATCAGA[-/T]TTTTTTTTTTATTAG | 50807 |
rs34113483 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271712 | CTGAACTAAACTTGC[-/T]TTCATTACCAGGATT | 50807 |
rs34126425 | in-del | -/A | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401393 | TGAGATTACAGTCAC[-/A]TGCTACCACACCCAG | 50807 |
rs34133505 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249614 | ATCTCTCTTCATTCA[-/G]CTAGTGCTATGAGAG | 50807 |
rs34136345 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208029 | ATGTATACTAAACAC[-/T]TTTCCCCTACTTTTC | 50807 |
rs34138357 | in-del | -/ACACACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420236 | TGGCCATAATGAAAT[-/ACACACAC]ACACACACACACACA | 50807 |
rs34140268 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094674 | AGAGCTGGGATAAGG[-/G]CAGGTGTCCAGGACT | 50807 |
rs34141564 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376904 | CAAAACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 50807 |
rs34143800 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161349 | CAGGATGGCTTCTTT[-/T]CTGACACTCAGGATC | 50807 |
rs34159694 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256448 | ACCACTCTGAATTCA[-/T]TTCATTTGGCACAAT | 50807 |
rs34161158 | in-del | -/T | 0.497091 | 0.0380279 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160546 | CAGCAGTGAAAAGTG[-/T]TATGATGTCGTGGAG | 50807 |
rs34179841 | snp | C/T | 0.162253 | 0.234095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393051 | CAGTTATATTATGAG[C/T]GTTCTCATAACTTAT | 50807 |
rs34180756 | snp | C/G | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391574 | AAAAACTTTGGTTCT[C/G]AATCTATCCTGCTGC | 50807 |
rs34188408 | multinucleotide-polymorphism | AC/GT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400207 | ACCCACACACTTTCC[AC/GT]TACGCGGACTTCTTA | 50807 |
rs34188811 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174713 | AATCTTCTAAACAAA[-/G]GGGGTTTAGAGAGCT | 50807 |
rs34200957 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392785 | TGTGCAGAGATCAGA[C/T]GGTGAGAGAAGGAGG | 50807 |
rs34209897 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196335 | GACAAGAGTGAAACT[-/C]CCATCTCAAAAAAAA | 50807 |
rs34226410 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130280565 | ATATAATTTAATAAT[-/G]CCTACTGGACTCTTC | 50807 |
rs34227813 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303713 | CTATATGACATTCTG[-/A]AAAAGGCAAAACTAT | 50807 |
rs34233859 | in-del | -/TA | 0.136166 | 0.22258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222261 | TTATCTAACTGACAC[-/TA]TGTGTTATACCTTAC | 50807 |
rs34235479 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102432 | GAAACATCCTTGCAT[-/A]CCCTGCGATAAATCA | 50807 |
rs34250532 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130152930 | AAATCCAACCCCCCC[-/CA]AAAAAAATCCTGGTT | 50807 |
rs34281474 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130322336 | AAATGCTGTAACTAA[-/C]ACATGATTCCTTCTC | 50807 |
rs34303787 | snp | C/T | 0.107694 | 0.205546 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105639 | GAAAGCTTAAGTTAA[C/T]TACTTTAAAAAGTAA | 50807 |
rs34317454 | in-del | -/T | | | frameshift-variant | ASAP1 | GRCh38.p7 | 8:130118648 | TGATCTACATACTTT[-/T]GCAGTGATATATTCT | 50807 |
rs34326035 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205363 | CTACCTTGAAACACT[-/G]GAATGTGAATCCTTA | 50807 |
rs34331765 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416695 | AATGCATTAGTGCCC[-/C]AAAAGGGGCAGGAGA | 50807 |
rs34334020 | snp | A/C | 0.379942 | 0.213577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392738 | GCCTCAGGTTGCTTC[A/C]ACTCGTGGCAGAAGG | 50807 |
rs34338606 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130436253 | TCTCACCTGTAATCC[-/C]TAGTACTTTGGAAGG | 50807 |
rs34338648 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331241 | CCTATTACCCCTTAG[A/C]CCATTCTCTGGAAGG | 50807 |
rs34344345 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312454 | CACTAAAAGGAGGGG[-/A]AAAAAAACCCATTAG | 50807 |
rs34379401 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191050 | ATAACCGGGAAATAG[-/T]TTTTTTTTTTTTTTC | 50807 |
rs34380724 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221586 | TTTCTGCTCTTTGCT[-/A]AAAATGGTATATAAG | 50807 |
rs34381679 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111435 | GCTTTGGTCACACAG[-/G]AACCTGGGTTAGAAT | 50807 |
rs34383827 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331051 | AGTTCCCCCAGCTGC[-/A]AAAAGGGAATAAGAT | 50807 |
rs34384744 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101404 | GCATTAATTCTTCCA[-/C]ATCATGAGCATGTGA | 50807 |
rs34387098 | snp | C/T | 0.298905 | 0.24517 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283983 | GAGTGGGTATTGCAC[C/T]GACTGTATCCACAAA | 50807 |
rs34402384 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130181895 | ATCCGTCAAGTCTTC[-/T]TTTAAGTTATGGTGG | 50807 |
rs34422467 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120310 | GCAGCTACTGTGTTG[-/C]ATGGATGGAGCAGCA | 50807 |
rs34429651 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302364 | TCGTTTTTTCACAGA[C/T]ACAGAAAATGTGGCA | 50807 |
rs34436294 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254662 | GTCTGTAAATTATGA[-/C]CCCTTATGTAAACAG | 50807 |
rs34438161 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392834 | CTTTTAAACAAACAG[C/T]TGTCACGGGAACTAA | 50807 |
rs34456271 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140128 | GTCTCAACCTCCTAG[-/G]CTCAAGCGATCCTCC | 50807 |
rs34456940 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068144 | GGATCCAACTCCCCA[G/T]GAGTTGGGGCACTGG | 50807 |
rs34471225 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074038 | AGGGGAAACTTTAGC[-/C]TAAGACACTTAGAGA | 50807 |
rs34484540 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145859 | TTTTTTTTTTTTTTT[-/T]GAGATGGGGTCTCAC | 50807 |
rs34492373 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392902 | GACCCAAACATTTCC[C/T]ATCAGGCCCCACCTT | 50807 |
rs34505485 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359316 | GCCAAATTTCGGTGG[-/A]AAAAGTACCACCTCA | 50807 |
rs34518677 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130240703 | AAATGAATACAGGAG[-/A]ATGTAAAGTTGTGCC | 50807 |
rs34531563 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311909 | AAAAAAAAATAGTAA[-/T]TTTGAATACGATCCA | 50807 |
rs34532721 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182911 | ATAAAAAAGCTAACT[-/G]GAAACAGTGGGGAAA | 50807 |
rs34542318 | snp | A/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401442 | TAGAGACAAGGTTTC[A/G]CCATGTTGGTCAGGC | 50807 |
rs34562395 | in-del | -/A | 0.495927 | 0.0449436 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228701 | GTGAGACCCTGTCTT[-/A]AAAAAAAAAAAAAAG | 50807 |
rs34568641 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282429 | GTCTATTGGTAAAAA[C/T]AAATCAAAATATTTT | 50807 |
rs34587973 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332917 | GAAGTTTTTTTTTTT[-/T]AAAGGGAAAATAATA | 50807 |
rs34615656 | in-del | -/A | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254838 | TTTTTCTTAAGTAGC[-/A]AACAACCAATCTAAC | 50807 |
rs34617761 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089047 | AGCACATGCCCTCAG[-/T]AAGGAGTTCATGTAC | 50807 |
rs34625354 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350321 | CCCTGGGTTGGGCAG[-/C]CCCTGAATTCAAATC | 50807 |
rs34626937 | in-del | -/A | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212561 | ATGAACAAGTTATAT[-/A]ATCTCAATTTGCCTC | 50807 |
rs34629557 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130220755 | AATTGACTCAGTTCA[-/C]GCCATGGCTGAGGAG | 50807 |
rs34635974 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112993 | TCCCTTGAAGCCCCT[C/T]CTAGTACAGGTGCTC | 50807 |
rs34642519 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274181 | GCATTGCTTTCCCTT[-/G]GGGGAAGTACCAACT | 50807 |
rs34651952 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331141 | CAGGCACACATATTA[-/C]AATGTCAGCTAATCT | 50807 |
rs34656350 | snp | C/G | 0.491525 | 0.0645418 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257830 | CTACTAATCTCAGAA[C/G]TAGTTCTCCATGTAA | 50807 |
rs34671004 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130330360 | CCCTGTAAGATTTCT[-/C]CCAGTTGGAACCTGT | 50807 |
rs34676374 | snp | A/G | 0.409041 | 0.192888 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410794 | GACACATTCCAACAC[A/G]GGCTCTCCCACCTAA | 50807 |
rs34680836 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130123927 | CCACTGCACCCAGCC[-/A]AAAAAAAAAAAAAGA | 50807 |
rs34692282 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434308 | CCACTGCACTACAGC[-/C]TGGGAGACAGAGTGA | 50807 |
rs34721076 | snp | C/T | 0.271972 | 0.249033 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415208 | GGAAACTGGGGATGC[C/T]TTTTAAACTACAGGG | 50807 |
rs34721219 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391471 | CCACAATTAAAATAT[C/T]TTAAAATAAAGATTT | 50807 |
rs34724088 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206124 | CCCACCAACCCACAT[-/G]GGATAGATCACATTT | 50807 |
rs34730078 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206469 | AAAAAAAAAAACAAC[-/T]TTTAACACAAACCAC | 50807 |
rs34737610 | snp | C/T | 0.40853 | 0.193309 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401354 | GGGTTCAAGCAATTC[C/T]ACTGCCTCAACCTCC | 50807 |
rs34751583 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130214382 | AAATCCTAGGCGACT[-/A]AAAAGCTTTTTAGTT | 50807 |
rs34799517 | in-del | -/AC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284843 | TTCCTTTTACACTCT[-/AC]ACACACACACACACA | 50807 |
rs34816649 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120188 | GGTCAAAGTCCTTTT[-/T]AGGATGGCTAGAGCC | 50807 |
rs34822664 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130125072 | ACTAACTGCCCTTTT[-/T]GGTTAAGGCTAATGA | 50807 |
rs34824172 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130332368 | CCACACCACCTGCAC[-/T]TTTTTGAATATTCAA | 50807 |
rs34857454 | snp | C/T | 0.262435 | 0.249691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224354 | GCATACTTTGTAGCA[C/T]TAATCACACTTATAA | 50807 |
rs34868705 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310824 | AATGCAGGAACAATT[-/C]CCATTTCCCTATATA | 50807 |
rs34870383 | snp | A/G | 0.00800401 | 0.062753 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130214613 | AAACTTGACAAACGC[A/G]GTGCCAAGGTCGGGG | 50807 |
rs34874442 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323697 | TGCAGACATCACTTG[-/C]CAAAGAATTTATCAT | 50807 |
rs34904133 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253247 | GCCAGAAACTTAACC[C/G]GGCTGTGCCTCAGTT | 50807 |
rs34905534 | in-del | -/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064893 | TCAGTTTACTAAGAA[-/TG]TGTGTGTGTGTGTGT | 50807 |
rs34933250 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257625 | ATTAATGCTGTTGCG[-/A]AAAAAAGGGATCTAC | 50807 |
rs34936340 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346753 | CAGTGTATTCACTTG[-/C]CCTTGCTATGAAAAA | 50807 |
rs34956760 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191064 | GTTTTTTTTTTTTTT[-/T]CCACTGCTCTGCGGC | 50807 |
rs34962169 | snp | C/T | 0.105569 | 0.204058 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313885 | CAATGCCACTGCACT[C/T]GACACCACGTCCCAT | 50807 |
rs34978580 | in-del | -/TT/TTT | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107200 | TTTTTTTTTTTTTTT[-/TT/TTT]GAGACGGAGTCTCAC | 50807 |
rs34987314 | snp | C/T | 0.409721 | 0.192325 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410440 | CAAGTTTATTCTATA[C/T]TCGGAGGGAGGCTAG | 50807 |
rs35004363 | in-del | -/A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074126 | TCTTAAAAAAAAAAA[-/A/G]GGGGGCAATTGTGAG | 50807 |
rs35009361 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129479 | CATGAATGAGAAAAA[-/A]GCCAAATTTATTTTC | 50807 |
rs35009497 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391746 | CATTTCAGTCCAATA[C/T]AGTAAATGTAATAAT | 50807 |
rs35009653 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130404874 | CTTATGATGCACCAC[-/A]AAAGGAATATGTCTC | 50807 |
rs35011453 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130430762 | TGTATTCAGAATTGG[-/T]TTTGGGTTGGAAGAA | 50807 |
rs35012366 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130258499 | ATCCTTCATTACTTT[-/C]CCAGTTGTTTCATGT | 50807 |
rs35020130 | in-del | -/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390933 | CTTCTGGGTATATAT[-/C/T]CCCCCGCCCCCCCAA | 50807 |
rs35025734 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177445 | TTTCTTTAAAACTTT[-/C]CAAAGGAATTAAATG | 50807 |
rs35046250 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162702 | GGCGCCTGTACTCCC[-/A]AGCTACTCAGGAGGC | 50807 |
rs35055966 | in-del | -/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257788 | GGACTCAAGAGCACC[-/G]CCCCCCCCATTATTT | 50807 |
rs35060121 | in-del | -/A | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382309 | AAAAAAAAAAAAAAA[-/A]GAAATTAAAGATATC | 50807 |
rs35062353 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399446 | CTGGACTCTTGACTT[-/A]AAAAAAGAAAAAAAC | 50807 |
rs35072710 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130255459 | AATAACCTTTGCATA[-/T]TTTTTTTTCCTGCAT | 50807 |
rs35075210 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420447 | AAGTGAAAATGTACA[-/A]TTCAAATAAATACTT | 50807 |
rs35077517 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338544 | CACAGTCATCCCAGC[-/A]AAACACTCTGCAGTA | 50807 |
rs35079970 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190793 | GTGCTGGGATTACAG[-/T]ACGTGAGCCACCGCA | 50807 |
rs35084445 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275876 | CGGAGAACAACAGAA[-/C]TGGAGGAGAACGTAA | 50807 |
rs35089636 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259933 | TCATAGGCAGCACCG[-/A]AAAATTATTTTAAAA | 50807 |
rs35091752 | snp | C/T | 0.499295 | 0.0187567 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387901 | ATGAGCAGCCATCAG[C/T]GACCTTGTCCATTAG | 50807 |
rs35104220 | snp | A/G | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391426 | TTAAAAACAGTTAAC[A/G]ATAGTAATTTTTATG | 50807 |
rs35117563 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359180 | GGTTTGGGGGCTTTT[-/A]AAAAAAATAATTTTC | 50807 |
rs35117671 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310139 | AATACAGTTTTTTTT[G/T]GGGGGGGGAGGGGGG | 50807 |
rs35118657 | snp | A/C | 0.409212 | 0.192748 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409271 | TGTCTCAAAAAAAAA[A/C]ACAAAAAACCTCCTC | 50807 |
rs35123370 | snp | C/T | 0.415235 | 0.18761 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410707 | CATCTGGGCAGCTGC[C/T]CCCTCATGCTGCAGC | 50807 |
rs35131449 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352161 | CCAAACATACTTTCT[C/T]TACATTAAGCAAAAG | 50807 |
rs35142045 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311085 | ACGCAGTCCAGGGCA[-/G]GGTTGTCAGAAATGT | 50807 |
rs35169399 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328611 | ATGGCTCAGTAGTTC[-/T]TTTTTTTTTTTTTTT | 50807 |
rs35172221 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423637 | TGGAAGGAGAGTCCC[-/C]TATATATTATATGAA | 50807 |
rs35177978 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130377209 | GATACAGTGAACTTT[-/G]GGGGACTCAGGGGGA | 50807 |
rs35183706 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301781 | CGACTGTCTTTCCAT[A/G]TCAACAGATATGCAT | 50807 |
rs35191776 | in-del | -/A/AA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092957 | AAAAAAAAAAAAAAA[-/A/AA]TTAAGGCTTTTCTAA | 50807 |
rs35195899 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182832 | AAACTATAAAAAGGC[-/AA]AAAAAAAAAAAAAAA | 50807 |
rs35197480 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130239493 | ACAGAGCCTTATCTT[-/G]CTAACCACTACCTAA | 50807 |
rs35199935 | in-del | -/A/CA | 0.499767 | 0.0107802 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188690 | GTGAGCCGAGATCAC[-/A/CA]CACTGCATTCCAGCC | 50807 |
rs35207670 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256849 | CTATAAAGGGAGGGG[-/C]ACAAATTTCCTTTGA | 50807 |
rs35210585 | in-del | -/C | | | splice-acceptor-variant | ASAP1 | GRCh38.p7 | 8:130079972 | GACCCCCATCGTTAC[-/C]TACAAGGAAAACCGA | 50807 |
rs35211252 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337054 | ATCTTTACAATAGGG[A/C]CAATCACAAATAGCT | 50807 |
rs35212783 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272136 | ACCACTGCACTACAG[-/C]CTAGGGGACAGAGCA | 50807 |
rs35220844 | snp | A/G | 0.161924 | 0.233971 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392814 | GGTGGGGGAGGGGCT[A/G]GGATCTTTTAAACAA | 50807 |
rs35229803 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400062 | CAACCTCAGGTGATC[C/T]GCCCACCTCGGCCTC | 50807 |
rs35232892 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218519 | ATTTCATGCAAAGGT[-/G]TAGAAAGAATTACAA | 50807 |
rs35235070 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190867 | GATTACTACAGCTTA[-/G]TAGTATAATTTGAAG | 50807 |
rs35244156 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275737 | TTTTCTAAATATTAT[C/T]CAAATAAACATAAAA | 50807 |
rs35245330 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130211366 | TTGTAGGTAGCCCTT[-/G]GGGAGTTTTCACATA | 50807 |
rs35256608 | snp | A/G | 0.49334 | 0.057322 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098349 | ACATTCTCATCTTTA[A/G]ACACTTTTTTGAGAT | 50807 |
rs35278606 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307039 | TTCCTTAAAGAGATA[-/C]CCTCTGGGCAATCCT | 50807 |
rs35298769 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232557 | TCATACACAACAAGG[-/G]AAAAGTGAGACACAA | 50807 |
rs35305115 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391536 | ATATATCAGTCCTCA[C/T]GGCTTTGAGAAAATA | 50807 |
rs35311325 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143380 | ACTGTTAATACCTTA[-/T]ATTTTACCAAGATGT | 50807 |
rs35321979 | in-del | -/AACT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119090 | TTGGTCGTCTGATAT[-/AACT]CTCTATTTTTTATTT | 50807 |
rs35338707 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342732 | TATAACTTGACTTTT[-/A]AAAAAGATGCCAACT | 50807 |
rs35346643 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177299 | CTATTTTGAAAAACT[-/C]CTTGTTTGTGTAGGC | 50807 |
rs35352314 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130430286 | CTCACCAAGATGAAT[-/A]AAAATGGCAAGGAGG | 50807 |
rs35357991 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329120 | CTGGATTTAACACTT[-/A]AGGGTATGAGAGCCC | 50807 |
rs35364242 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130309500 | ATCATAAGATGAGGC[-/A]CGGTATGCAACTGCT | 50807 |
rs35374618 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396003 | CAAGTTTGTGGTACT[-/A]TTGTCACAGCAGCCC | 50807 |
rs35374936 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130308920 | GGTGGTGTGCGCCTC[-/A]AAAAAAAGAATGACA | 50807 |
rs35386978 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206468 | ATAAAAAAAAAAACA[A/C/T]CTTTAACACAAACCA | 50807 |
rs35401019 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387007 | ACTATGGTGACTCAC[-/A]AAAAGTTATCCCACG | 50807 |
rs35420210 | in-del | -/AA/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376930 | AAAAAAAAAAAAAAA[-/AA/G]GTCTTGCTCTCCAGT | 50807 |
rs35427556 | snp | A/G | 0.49931 | 0.0185575 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382676 | ACATGGTGAAACCTC[A/G]TTTCTATTAAAAATA | 50807 |
rs35429166 | in-del | -/A | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073391 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAC | 50807 |
rs35447339 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223138 | TTATAAAACCACAAA[-/G]GGATTATTTCTACTT | 50807 |
rs35447484 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222262 | TATCTAACTGACACT[-/AT]GTGTTATACCTTACC | 50807 |
rs35447783 | in-del | -/T | 0.209997 | 0.246779 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359634 | TGCCATCTTGCACTG[-/T]TTTTTTTTTTTTTTT | 50807 |