SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9174 | snp | C/T | 0.494174 | 0.0536558 | synonymous-codon, nc-transcript-variant | ANAPC4 | GRCh38.p7 | 4:25417661 | CCGTACCATGCATTT[C/T]GAGAAGCACTGGAGA | 29945 |
rs186408 | snp | A/G | 0.251014 | 0.249998 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25389962 | TTTGAAAAAAGGAAT[A/G]AGCCTGATGTGACTG | 29945 |
rs315664 | snp | C/T | 0.247337 | 0.249986 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25409021 | ggtatgatttgggac[C/T]actaccttgactctt | 29945 |
rs315665 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25407071 | TTTTCTTTTATAGAT[G/T]ATAAGACACACAAAC | 29945 |
rs315666 | snp | A/G | 0.245631 | 0.249962 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25387180 | TCTGCATTAGTGTGT[A/G]TAGTCAAGTAATACA | 29945 |
rs315667 | snp | A/G | 0.00183583 | 0.0302414 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25391052 | CGGTAGAGAGTAAAT[A/G]TGTATTTAACAGGTT | 29945 |
rs315668 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25393003 | gccctggagtcaaca[A/G]tgttatttctgctgc | 29945 |
rs315669 | snp | A/C | 0.318896 | 0.240319 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25393163 | TCTAGAGATCAGTAT[A/C]TTTTTAAAATTGAAT | 29945 |
rs315670 | snp | A/C | 0.319136 | 0.24025 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25393190 | GAATAATTGACCAAA[A/C]CAGTATTTTGACAGT | 29945 |
rs315671 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25394009 | AGATCATAATTTCTT[A/T]CAAATGGCTTCGTCT | 29945 |
rs315672 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25398568 | ccaggttgcatagag[C/T]ctgtgggcagttgtt | 29945 |
rs315676 | snp | C/G | 0.367913 | 0.220446 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25380594 | TAAAAAGTTCCCAAA[C/G]TGATATTTATAATTC | 29945 |
rs315677 | snp | C/T | 0.27893 | 0.24832 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25380159 | CCTGTACCTAATCTT[C/T]TATGTCAACGGGAGA | 29945 |
rs315678 | snp | A/G | 0.278399 | 0.248382 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25378105 | TCCTTGTCCAATTTA[A/G]AGGTATTTTTAGTGG | 29945 |
rs315679 | snp | G/T | 0.282105 | 0.24793 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25377147 | GTCCCTGTCCGCCCC[G/T]TCTGGCTCTCAGCAC | 29945 |
rs315680 | snp | C/T | 0.383439 | 0.21141 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25376164 | CGCCTCACTGCAAGC[C/T]CCGCCTCACTGCAAG | 29945 |
rs315681 | snp | C/T | 0.224116 | 0.248656 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25376125 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 29945 |
rs315682 | snp | A/G | 0.283421 | 0.247756 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25375570 | GTCACGGGCTTTGCA[A/G]CCCTTGCCTTTGCCA | 29945 |
rs316770 | snp | C/T | 0.119978 | 0.213528 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25404376 | ACCTTAGAAGACTTT[C/T]TTTTTGCAGAGGTAG | 29945 |
rs364071 | snp | C/T | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25404539 | ATCCTTACTACATAT[C/T]CTAACTGTAGTAAGA | 29945 |
rs369536 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25376147 | cggctcactgcaagc[C/T]ccgcctcactgcaag | 29945 |
rs395431 | snp | A/G | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25405952 | GAAATCAGGTGCTTA[A/G]ATATTAGTCCCTGTG | 29945 |
rs416299 | snp | C/T | 0 | 0 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25404488 | ATTGTCCTTACTACA[C/T]ATTCTAACTGTAGTA | 29945 |
rs418952 | snp | C/T | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25404448 | TCTATCCTTACTACA[C/T]ATTCTAACTGTAGTA | 29945 |
rs451500 | snp | C/T | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25404567 | AGAATCCTTACTACA[C/T]ATTCTAACTGTAGTA | 29945 |
rs454026 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25394505 | taattgatacataat[A/G]tgttacatacttacg | 29945 |
rs908056 | snp | A/G | 0.437542 | 0.165312 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25392909 | CCTTCATACTCCAGC[A/G]AGCCAGCACAGGCTT | 29945 |
rs1017716 | snp | G/T | 0.491629 | 0.0641526 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25416709 | TTTCGTTACTAGAGA[G/T]AACCACAGAGGTAGC | 29945 |
rs1380113 | snp | A/G | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25411090 | TTCTTTTTCAAGGCA[A/G]AACCTATTATGTATT | 29945 |
rs1533133 | snp | C/T | 0.43978 | 0.162738 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25382683 | CATGTGATGGTGATA[C/T]GCAGTGAAACTCACT | 29945 |
rs1993602 | snp | C/T | 0.424503 | 0.179021 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25413484 | GGCAGAAGACCATGG[C/T]CGTTTTTAATGAGGT | 29945 |
rs2012277 | snp | C/T | 0.421051 | 0.182323 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25406182 | TGGACAGCATTAAAA[C/T]TAGCCTCATGAGCTA | 29945 |
rs2012284 | snp | C/T | 0.420892 | 0.182472 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25406052 | CCAGTGATGGAATCT[C/T]CTTCCAGGGAAGTCT | 29945 |
rs2012286 | snp | A/G | 0.421684 | 0.181726 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25406039 | AGGACTGTGACAACC[A/G]GTGATGGAATCTTCT | 29945 |
rs2045530 | snp | C/T | 0.170408 | 0.236992 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25388098 | CACACCACTGCACTC[C/T]GGCCTGGGTGAGACC | 29945 |
rs2168971 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25401693 | CTGCATCAGTCTTCC[G/T]TCACTTTTGACATTT | 29945 |
rs2168972 | snp | C/T | 0.421526 | 0.181876 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25416029 | TTTTATGATAAAGTC[C/T]TTGGAGTTGCTGTGC | 29945 |
rs2271388 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25388415 | GTTGTAAAACTGGGT[A/G]TCTTTTTTAAAAATT | 29945 |
rs2271389 | snp | A/G | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25391106 | TCACTGTATTGTAAT[A/G]ATCATTAAAATAATG | 29945 |
rs2292405 | snp | C/T | 0.164219 | 0.234823 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25383118 | TTCTTTTTTTAGTTT[C/T]TAAAATATTGAAGGA | 29945 |
rs2292406 | snp | A/T | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25391853 | TCATATTTGCTCATC[A/T]TCTTAAGGTTATGTG | 29945 |
rs2292407 | snp | C/T | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392267 | ATACGTAGTTTGACC[C/T]ACACTCTAAATTACA | 29945 |
rs2292408 | snp | A/G | 0.496906 | 0.0392072 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392456 | TTTATGTGAATATTT[A/G]TTATCGGCTTCTAAA | 29945 |
rs2292409 | snp | C/T | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392599 | ATTGAGAACCTACTT[C/T]CACCGCACCCTATTT | 29945 |
rs2292410 | snp | A/G | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392717 | TTCACATGAGTTTAC[A/G]TTTGTTCATAATAAA | 29945 |
rs2305953 | snp | G/T | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25409580 | AAAAATAAACCGATT[G/T]TAGGCCCTAAGTCTT | 29945 |
rs2305954 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25413485 | GCAGAAGACCATGGT[C/T]GTTTTTAATGAGGTT | 29945 |
rs2324712 | snp | A/G | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25412364 | gaactcaacctccaa[A/G]cccctctctcttcct | 29945 |
rs2324761 | snp | C/T | 0.286825 | 0.247273 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25381161 | TAAGAAAAAAGTGAA[C/T]TGTTTTTGTAAAATA | 29945 |
rs3214034 | snp | A/T | 0.496326 | 0.0430272 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25406894 | CAATGAGGTAAGAAG[A/T]TGATATTTCTGTAAT | 29945 |
rs3214035 | snp | A/T | 0.13519 | 0.222078 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ANAPC4 | GRCh38.p7 | 4:25415487 | GAGTAATGGACTAAT[A/T]GCTATTAAATTTGGG | 29945 |
rs3214036 | snp | A/G/T | 0.0192304 | 0.0961541 | synonymous-codon, nc-transcript-variant | ANAPC4 | GRCh38.p7 | 4:25418286 | GGAAGAAGTGTTGTC[A/G/T]GAGTCAGAGGCAGAG | 29945 |
rs3215196 | in-del | -/CA | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392697 | GTATTGTGGGAAAAA[-/CA]GTCTTCACATGAGTT | 29945 |
rs3756202 | snp | C/T | 0.278664 | 0.248351 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25405734 | TTAAGGGATCTAACG[C/T]CTACATCCTGACATC | 29945 |
rs3816585 | snp | C/G | 0.0810805 | 0.184299 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25414258 | AGTGATGGTCAGTCA[C/G]TTTCTGTAGAGTATC | 29945 |
rs3816586 | snp | G/T | 0.421368 | 0.182025 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25415155 | AATTGAAAGTAGAAG[G/T]TCTGAAAAATAAATC | 29945 |
rs3816587 | snp | C/T | 0.495963 | 0.0447464 | intron-variant, downstream-variant-500B | ANAPC4 | GRCh38.p7 | 4:25415622 | GATCAGACTCAGTTA[C/T]GGTGGTAATATAGGT | 29945 |
rs3822217 | snp | A/G | 0.433236 | 0.170072 | upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25377097 | AGGGAGGAGCGAGGG[A/G]CGGATCGAGGTGGGG | 29945 |
rs4317194 | snp | C/T | 0.437542 | 0.165312 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25392855 | TCATGCCAGCTGGTA[C/T]GTGTCCCTTGGCTGT | 29945 |
rs6448354 | snp | A/C | 0.439363 | 0.163222 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25387962 | AGACCCCCATCTCTA[A/C]AAAAAAAAATGTATA | 29945 |
rs6448355 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25412295 | tgtcccagtgtattt[A/C]tggcggtttcattat | 29945 |
rs6814162 | snp | A/G | 0.439224 | 0.163383 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25387879 | TAGTGGTTCATGCCT[A/G]TAATCCTAGCACTTT | 29945 |
rs6819212 | snp | C/T | 0 | 0 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25414918 | TTGGCATATAATCAT[C/T]GTAGGACTTTTTTTA | 29945 |
rs6830160 | snp | G/T | 0.191267 | 0.243003 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25377604 | GGTCTGCTCCCGGGG[G/T]GCCCAAGAACACCGA | 29945 |
rs6831977 | snp | C/G | 0.421209 | 0.182174 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25402730 | GTTTGTGGCAAGGCT[C/G]TTGTAACCAGTTGGA | 29945 |
rs6834554 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25413420 | GGTGAGTCTAAGTTT[A/G]TAGTAAGTGAGATTG | 29945 |
rs6835099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25383795 | gctaaaaaatgctaa[C/T]gatcatctgagcttt | 29945 |
rs6836283 | snp | A/T | 0.122064 | 0.214785 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25408537 | ccaaaaAAAAAAAAA[A/T]tttttttttttttga | 29945 |
rs6848308 | snp | C/G | 0.437683 | 0.165152 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25392779 | TTGGTGATTTAGGCT[C/G]AGCTTAGCCAAGATG | 29945 |
rs6849634 | snp | A/G | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25410385 | AATCTGACCAGATTT[A/G]GCAATTGCTTAGATC | 29945 |
rs6856574 | snp | C/G | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25411185 | GATAAAGGTACAGGA[C/G]ACGCTACTTATTTAC | 29945 |
rs7435058 | snp | A/C | 0.422684 | 0.183196 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25412299 | ccagtgtatttctgg[A/C]ggtttcattatgtag | 29945 |
rs7658636 | snp | A/G | 0.456685 | 0.140646 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25412589 | ACATAGTGAAACCCT[A/G]TCTCTACTAAAAATT | 29945 |
rs7661300 | snp | C/T | 0.439502 | 0.163061 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25384252 | cccatcttcaggctc[C/T]acttctaattctagt | 29945 |
rs7663274 | snp | C/T | 0.435407 | 0.167703 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25409357 | TCTTTTAATACTTTG[C/T]GGTTTGTTTAGTTGC | 29945 |
rs7684466 | snp | C/T | 0.439363 | 0.163222 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25384846 | ACCATTTGACCCATA[C/T]GATGCAGAATGGATT | 29945 |
rs7698046 | snp | C/T | 0.278133 | 0.248412 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25411313 | TTGGCTATTATTGAT[C/T]CAGGGAACTTTGCCA | 29945 |
rs9654100 | snp | G/T | 0.437542 | 0.165312 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25396073 | CTCTTGTCCCAACTT[G/T]TTCTTCACATGCATT | 29945 |
rs9991246 | snp | C/T | 0.439363 | 0.163222 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25383698 | AAAGTTATGTTTATA[C/T]TATGCTATAGTACAT | 29945 |
rs9993416 | snp | A/G | 0.421684 | 0.181726 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25400113 | cagagaagacagcaa[A/G]tatagcctcttgagg | 29945 |
rs9993776 | snp | A/C | 0.421842 | 0.181577 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25400484 | agagtaaggatgggg[A/C]ggcggtgttggaggt | 29945 |
rs9996892 | snp | A/C | 0.421526 | 0.181876 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25401341 | GAGCTTTGCTTCAGG[A/C]TACTGGTGCCCACGT | 29945 |
rs10001307 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25390361 | TCAGAGACTAATTTC[C/T]TTACTAAGATAAAAT | 29945 |
rs10001352 | snp | G/T | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25411352 | ATAGGTCCTGTCCTC[G/T]TTTATTTGCCCCACA | 29945 |
rs10004635 | snp | A/G | 0.114036 | 0.209795 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25384328 | gtgttgaacccctca[A/G]agtcatccatgaggg | 29945 |
rs10005501 | snp | A/G | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25409367 | CTTTGTGGTTTGTTT[A/G]GTTGCTTGACTAAAC | 29945 |
rs10005866 | snp | G/T | 0.437542 | 0.165312 | intron-variant, upstream-variant-2KB | ANAPC4 | GRCh38.p7 | 4:25393278 | AAAAATTTAAGAATG[G/T]TTTATTATGAAATTC | 29945 |
rs10016263 | snp | G/T | 0.421684 | 0.181726 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25400178 | agcagaattgctggg[G/T]ttttttcttcttttt | 29945 |
rs10016572 | snp | G/T | 0.421842 | 0.181577 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25400485 | gagtaaggatgggga[G/T]gcggtgttggaggtt | 29945 |
rs10020325 | snp | A/G/T | 0.114036 | 0.209795 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25389159 | caccacacccagcta[A/G/T]ttttttttttttttt | 29945 |
rs10020759 | snp | A/C | 0.118933 | 0.212888 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25389627 | CTTCAAACAATATAT[A/C]GACCTTAATATCTAT | 29945 |
rs10023139 | snp | C/T | 0.489363 | 0.0721468 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25402931 | TATGAATCCCCCACA[C/T]ACTAATCTTATTTCT | 29945 |
rs10026762 | snp | A/C | | | intron-variant | ANAPC4 | GRCh38.p7 | 4:25414024 | TTCATTGTAAACAGT[A/C]TTAGTTACAGAGCTG | 29945 |
rs10027814 | snp | A/G | 0.439502 | 0.163061 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25384937 | tgaccagtcatgaat[A/G]agcaataatattttg | 29945 |
rs10027825 | snp | A/G | 0.439502 | 0.163061 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25384977 | ttttttcagagcagt[A/G]ggcctcaacagtgga | 29945 |
rs10031316 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25410651 | gttgagcatcttaat[C/T]caaaaatctgaaatc | 29945 |
rs10032586 | snp | A/G | 0.141258 | 0.225111 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25398846 | agggagtcatagata[A/G]ttatgagtttagggc | 29945 |
rs10033436 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25386396 | ttttatatttttagt[A/G]gagacgggatttcac | 29945 |
rs10034844 | snp | A/G | 0.420733 | 0.18262 | intron-variant | ANAPC4 | GRCh38.p7 | 4:25411987 | aaatgtcaggtctct[A/G]ggtccccacatctct | 29945 |
rs10517073 | snp | A/G | 0.499784 | 0.0103811 | intron-variant, downstream-variant-500B | ANAPC4 | GRCh38.p7 | 4:25415749 | CCTGCAGTTTATGTC[A/G]TACGGTTTCCTATAA | 29945 |