SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13141 | snp | A/G | 0.011718 | 0.0756419 | missense | ANAPC5 | GRCh38.p7 | 12:121318281 | GATCGGCTTACCTGC[A/G]CAAAAGCCAAGTTCA | 51433 |
rs15289 | snp | A/T | 0.00673393 | 0.0576335 | utr-variant-3-prime | ANAPC5 | GRCh38.p7 | 12:121308437 | GACATGAACAAGTCC[A/T]AAATCTTATACTCTG | 51433 |
rs938107 | snp | C/T | 0.499053 | 0.0217445 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326361 | CACAGCAGTGTTTAC[C/T]GAGATGGAGGGCTTT | 51433 |
rs1135180 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332975 | aaaaatatagagaca[A/G]ggttttggtatgttg | 51433 |
rs1135181 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332967 | AGAGACAAGGTTTTG[C/G]TATGTTGCCCAGGTT | 51433 |
rs1135182 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332965 | agacagggttttggt[A/G]tgttgcccaggttgt | 51433 |
rs1135183 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332931 | tgaacgcctggtctc[A/G]agtgatcctcccacc | 51433 |
rs1135184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332930 | gaacgcctggtctca[A/G]gtgatcctcccacct | 51433 |
rs1135185 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332903 | accttggcctcccaa[A/G]gtgctgggattatag | 51433 |
rs1169961 | snp | A/C | 0.484701 | 0.0861117 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347992 | AATAATCACTCCAAA[A/C]ATGCAAATAAGGATT | 51433 |
rs1169962 | snp | A/T | 0.492533 | 0.0606443 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348669 | GACTCCGTCTCCAAT[A/T]AAAAAAAAAGAGTAC | 51433 |
rs1169963 | snp | C/T | 0.418814 | 0.184396 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348980 | ATTAAAAAGACCATT[C/T]GGggcctggcgcagt | 51433 |
rs1169964 | snp | A/C | 0.332106 | 0.236133 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349165 | caaagtCTAGGCACC[A/C]AGCCAAAAATTAACT | 51433 |
rs1617736 | snp | C/T | 0.251296 | 0.249997 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354289 | AGGCCTGAGCCACTG[C/T]GCCTGGATGCATGGC | 51433 |
rs1622534 | snp | A/C | 0.492137 | 0.0622048 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351757 | ccactgcgcccggcc[A/C]GGTTTTATGGCATTT | 51433 |
rs1647256 | snp | A/T | 0.36796 | 0.220421 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352084 | TCCGCACAGAGCAGA[A/T]GCTCAGTAAAAGTTT | 51433 |
rs1706462 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349039 | GGAGGCTGAAGCAGG[C/T]AGATTACTTGAGGTC | 51433 |
rs1706463 | snp | A/G | 0.466412 | 0.125164 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349040 | GAGGCTGAAGCAGGC[A/G]GATTACTTGAGGTCA | 51433 |
rs1799525 | snp | A/C | 0.478096 | 0.102335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352124 | GCAGGAGCCAGCGGG[A/C]GCCTCTCACCTGCAG | 51433 |
rs2089886 | snp | A/G | 0.286042 | 0.247388 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323973 | GGAAAGAGCAAAGGA[A/G]AATGGTTATATTAGA | 51433 |
rs2280067 | snp | C/T | 0.455144 | 0.142885 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330445 | ATTAATAATTAAAGT[C/T]ATATGAAACTGCCAA | 51433 |
rs2393834 | snp | C/T | 0.175897 | 0.238765 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313186 | CAAAAATTAGCCAGG[C/T]GTGGTAGCATGCGCC | 51433 |
rs2461474 | snp | C/G | 0.415563 | 0.18732 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316452 | AAAACAGGTATTCAA[C/G]CCCGGGCGCGGTGGC | 51433 |
rs2668242 | snp | G/T | 0.268452 | 0.249318 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319114 | tgtgtgtgtgtgtgt[G/T]tgtgtatacacagca | 51433 |
rs2668243 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317473 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 51433 |
rs2668244 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316914 | TATCAGTGCTTCATT[C/G]TTTTTCATGGCTGAA | 51433 |
rs2668259 | snp | G/T | 0.486855 | 0.0799975 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350530 | CCACGCCCGGCTAAT[G/T]TTTTGTATTTTTAGT | 51433 |
rs2668260 | snp | A/G | 0.472709 | 0.11358 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350419 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 51433 |
rs2668261 | snp | C/T | 0.361474 | 0.223771 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350310 | GAAACAGATCTGGGT[C/T]CCTGGGCCTCTATAT | 51433 |
rs2668262 | snp | C/T | 0.418653 | 0.184544 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350299 | GGGTCCCTGGGCCTC[C/T]ATATTATGGGATCTT | 51433 |
rs2686357 | snp | G/T | 0 | 0 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307939 | GCTCCTGGTCATTGG[G/T]CCAAAAATTATGAAA | 51433 |
rs2686358 | snp | C/T | 0.44858 | 0.151875 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315910 | tcttagacatgatac[C/T]aaaagcacaagcaac | 51433 |
rs2686359 | snp | G/T | 0.445196 | 0.1562 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318839 | GCCTGGCCAACATGG[G/T]GAAACCCTGCCTCTA | 51433 |
rs2695142 | snp | A/G | 0.433818 | 0.169443 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355688 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 51433 |
rs2695143 | snp | A/G | 0.474903 | 0.109173 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350488 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 51433 |
rs2942064 | snp | A/G | 0.305989 | 0.24365 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319857 | TAAGTACAAAATGGC[A/G]AATGTTCATCTTAAT | 51433 |
rs2942065 | snp | A/T | 0.44546 | 0.155869 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319954 | TGGGGGGATTTAAAA[A/T]TTTTTTAAAATATCT | 51433 |
rs2942067 | snp | A/G | 0.445724 | 0.155538 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317758 | AAATTCTTCCAGTGC[A/G]TTTGACCTTCACTCA | 51433 |
rs2948123 | snp | A/G | 0.44638 | 0.154709 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311758 | ggatcacttgagctc[A/G]ggcagttgagggtgc | 51433 |
rs2948124 | snp | C/G | 0.0618563 | 0.164627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312334 | tctgtgaggctgagg[C/G]gggtggatcacctga | 51433 |
rs2948125 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314620 | aacaaaataaggaca[C/T]acacttttttttttt | 51433 |
rs2948127 | snp | A/G | 0.41507 | 0.187755 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316768 | AAAAAGAAAACAGGT[A/G]TTCAAACAAAAGCTG | 51433 |
rs2948129 | snp | G/T | 0.446118 | 0.155041 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320159 | TATCATTCTCATTCA[G/T]GTTTTTTATACTTTT | 51433 |
rs2950417 | snp | C/T | 0.473174 | 0.112665 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350663 | GACGGAGTCTCGCTC[C/T]GTCGCTCAGGCCAGA | 51433 |
rs3751162 | snp | C/T | 0.297267 | 0.245491 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335749 | AAATAATCAATGTAT[C/T]TTAAACGCTGTAAAT | 51433 |
rs4980984 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312680 | ccaccgcactccagc[C/T]taggcgacagagcga | 51433 |
rs4980985 | snp | C/T | 0.31014 | 0.242659 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336443 | AGCACTTTGGGAGGC[C/T]GAGGAGGGTGGATCA | 51433 |
rs4980992 | snp | C/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312685 | gcactccagcctagg[C/G]gacagagcgagactc | 51433 |
rs4980993 | snp | A/C | 0.286042 | 0.247388 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326996 | ACAGTGTCGAGCAGA[A/C]CTGTCCAACACGTGT | 51433 |
rs7132036 | snp | G/T | 0.481319 | 0.0948228 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352718 | TGTTGGTTGTTGTTG[G/T]TGGTGGTGGTGGTGG | 51433 |
rs7132039 | snp | G/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352738 | ggtggtggtggtggt[G/T]gtCGttgttgttgtt | 51433 |
rs7133933 | snp | G/T | 0.241914 | 0.249869 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341102 | cgggaggcagaggtg[G/T]cggtgagctgagatt | 51433 |
rs7136642 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332942 | cacttgagaccaggc[A/G]ttcaagaacaacctg | 51433 |
rs7297531 | snp | G/T | 0.415235 | 0.18761 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322048 | tatttgtatttttag[G/T]agagacagggtttca | 51433 |
rs7954151 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349565 | tgagatcccaccact[C/G]taaaaaaattaaaaa | 51433 |
rs7954711 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349852 | gctgggactacaggc[A/G]cacatcacaatgccc | 51433 |
rs7954852 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349988 | agtgccggggttaca[A/G]gtgtgatcccacccg | 51433 |
rs7955965 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344905 | CTCTAAGTTCCAaag[C/G]gtttaggcagaaaag | 51433 |
rs7957078 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332724 | CCCATAGATCCAAGA[C/T]CAGAAACAAAGAAGC | 51433 |
rs7963796 | snp | A/G | 0.298144 | 0.245321 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339749 | gctgggattacaggc[A/G]tgagctgccacgccc | 51433 |
rs7970741 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337693 | ACCGACGCCCATGCC[C/T]AGCTCATCCTCTGGG | 51433 |
rs7971785 | snp | G/T | 0.399432 | 0.200425 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332518 | TCACTATCTGAGATA[G/T]TACAACTATGCTTAG | 51433 |
rs9668513 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342196 | TCTCCTCAGAACTAG[G/T]AAAGAAAAACATAAA | 51433 |
rs9738248 | snp | A/C | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342166 | TGTATCGAAAGAGTT[A/C]AAAAAATTTAACTCT | 51433 |
rs9738904 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342165 | TTGTATCGAAAGAGT[C/T]CAAAAAATTTAACTC | 51433 |
rs10400462 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341857 | GTGCTTCGTTAGTGA[A/G]GCAGAGGGGACCAAG | 51433 |
rs10400545 | snp | A/G | 0.110519 | 0.207473 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341930 | ACGGGCCTATGCCAC[A/G]ACACACATCACAGGA | 51433 |
rs10744759 | snp | C/T | 0.288127 | 0.247076 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325179 | AAAAAAAATTAAAAA[C/T]TGGCTGGGCGCGGTG | 51433 |
rs10744760 | snp | C/T | 0.26326 | 0.249648 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329656 | atttcattcttgttg[C/T]ccaggctggagtgca | 51433 |
rs10774591 | snp | A/G | 0.287867 | 0.247116 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326067 | TCAGAAAACATGGGC[A/G]GTGCTTCCCAGACAT | 51433 |
rs10849866 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321722 | TTTGTATTTTTAGTA[A/G]AGGCAGTGTTTTGCC | 51433 |
rs11065524 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321650 | AATTCTGATGTCTTA[A/G]CCCCCACCTCCCGAG | 51433 |
rs11065526 | snp | A/G | 0.365646 | 0.221644 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340041 | GAAAGCTCTggccag[A/G]cgcagtggctcacgc | 51433 |
rs11065527 | snp | A/T | 0.305186 | 0.243833 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343210 | ATAAGAAAAGTCTGA[A/T]TTTTAACATTTCTGC | 51433 |
rs11065528 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343510 | ggcagaggagcagca[A/G]gccaacctggggatc | 51433 |
rs11065529 | snp | G/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351525 | tgcagtggcgcgatc[G/T]cggctcactgcaacc | 51433 |
rs11408254 | in-del | -/T | 0.437683 | 0.165152 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349720 | GAATCACTGTTTCTA[-/T]TTTTTTTTTTTTTTT | 51433 |
rs11448974 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349721 | AATCACTGTTTCTAT[-/T]TTTTTTTTTTTTTTT | 51433 |
rs11457183 | in-del | -/A/AA | 0.495291 | 0.0482933 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350680 | AAAAAAAAAAAAAAA[-/A/AA]TCCTCTCCATGAGTG | 51433 |
rs11503159 | snp | A/G | 0.116809 | 0.211566 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339896 | TTTTTTTTTTTCCCA[A/G]ATGGAGTGTCGTTCT | 51433 |
rs11541849 | snp | A/G | | | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345866 | GTGAAAGAAAAATGG[A/G]AAAAGAAGAACTTGA | 51433 |
rs11541850 | snp | C/T | 0.0573584 | 0.15934 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352375 | GACAACTGGCGGCAG[C/T]GCGCCGCGGGCCCGA | 51433 |
rs11610335 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345418 | TAGGGGAAAGGACAG[A/C]GAAGTCATAAGACAC | 51433 |
rs11611253 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315274 | aaagctacaaaacat[G/T]gttgaagtaagttaa | 51433 |
rs11613001 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342790 | tttgatcccgggagg[C/T]ggaggttgcagcgag | 51433 |
rs11614079 | snp | G/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329105 | ATTCTGTACGTATGA[G/T]TTTCTTTCCCAGGTG | 51433 |
rs11614093 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329198 | ttgctctgtcgccca[G/T]gctggagtgcagtgc | 51433 |
rs11614859 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342808 | aggttgcagcgagcc[A/G]agatcacgccactgc | 51433 |
rs11615493 | snp | C/G | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336709 | caaaCACTGTTTTTT[C/G]CATCAGTCTAGTATA | 51433 |
rs11616052 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348370 | GCTGAAGTCTATAAA[A/G]AGTATGACGAGAggc | 51433 |
rs11831548 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335063 | TCCTATCTTCTTTTT[A/T]AAAAATACATTTTTT | 51433 |
rs11831561 | snp | A/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335166 | AGCAAATCtttattt[A/T]ttttttctttttttt | 51433 |
rs11835448 | snp | A/C/T | 0.0241279 | 0.107592 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333492 | AAGAAAGGCTCTGAT[A/C/T]GAGAGGTTATTAAAT | 51433 |
rs11835527 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333770 | ctctcaatcttctcc[C/T]gtagccataccctca | 51433 |
rs11836127 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334727 | AGCAAACCTGACTTT[C/T]AGTAAGCCTATGTAG | 51433 |
rs11836319 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335413 | tcacgtgatccaccc[A/G]ccttggcctcccaaa | 51433 |
rs11837857 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343722 | CCCATTTATAAACAA[C/T]GTCACCCCCTGCCAC | 51433 |
rs12228261 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312297 | ggctgggcgcagtgg[C/T]tcatgcctgtaatcc | 51433 |
rs12228568 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312594 | tgcctgtagttccag[C/T]tactaaggaggctga | 51433 |
rs12301472 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334127 | CAAAAAATAATTTTT[A/T]AAAAAATTAGCTGGG | 51433 |
rs12303740 | snp | G/T | 0.116138 | 0.211142 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354262 | CTCCGCCTCCAAAAG[G/T]GCTGGGATTACAGGC | 51433 |
rs12321214 | snp | C/T | 0.141596 | 0.225274 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332101 | CAGCCTCCCAAGTAA[C/T]TGGGACTACAGGCTC | 51433 |
rs12368808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318950 | gcttgaacccaggag[A/G]cagagattgcagtga | 51433 |
rs12369119 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315765 | gcagaagaataagag[C/T]ggagccctatctcat | 51433 |
rs12579382 | snp | C/T | 0.243633 | 0.249919 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332621 | CCCTAGTACCTACAA[C/T]AGTGCCTAGTACACA | 51433 |
rs12582191 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317927 | TTTCCAAAAGCTTTC[A/G]ATGAACATCTGTGTT | 51433 |
rs12582728 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331852 | TATGTTTGTTTGTTT[G/T]TTTTTTAGAGACAGG | 51433 |
rs12809143 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351758 | cactgcgcccggccC[C/G]GTTTTATGGCATTTT | 51433 |
rs12810194 | snp | G/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351760 | ctgcgcccggccCGG[G/T]TTTATGGCATTTTTA | 51433 |
rs12819229 | snp | G/T | 0.078151 | 0.181571 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336015 | GATAGATGAGAATAC[G/T]GGGCCTTACCTAGTT | 51433 |
rs12821054 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339946 | cagtggtgtgatctc[A/G]gctcactgtaacctc | 51433 |
rs12830931 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337791 | CTCTGCACTTACCCC[C/T]CCTGTGGCACTATCA | 51433 |
rs17850069 | snp | A/G | | | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121319809 | TTTTTTGATCACATA[A/G]CATCCATAACTAGTA | 51433 |
rs33999891 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334030 | TTGTAATCCCAGCAC[-/T]TTTGGAAGGCCAAGG | 51433 |
rs34016648 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326721 | AAAATAGGCACAGGG[A/G]CTGGCACAGAACAAA | 51433 |
rs34155676 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313991 | GCAAAAATTCTCAAC[-/A]AAAATACTTGCAAAC | 51433 |
rs34301487 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333129 | GAGACCATCCTGACC[A/G]ATATGGTGAAATCCC | 51433 |
rs34467784 | in-del | -/A/AA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351924 | CAGACATGAACTTGC[-/A/AA]AAAAAAAAAAAATGC | 51433 |
rs34514383 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325644 | GCTGAGGCAGGCGGA[-/T]TCACCTGAGGCCAGG | 51433 |
rs34606348 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335078 | AAAAAATACATTTTT[A/T]AAAAATGCATCACAA | 51433 |
rs34705650 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350901 | ACCACAACTGATATA[-/G]GGGGAAGGTATATGC | 51433 |
rs34780788 | snp | A/G | 0.375 | 0.216506 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318067 | TGAATACACAGCTCA[A/G]GAAAGCCAGTGCCAC | 51433 |
rs34791908 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312706 | GCGAGACTCTGTCAC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs34820493 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334046 | TTGGAAGGCCAAGGT[-/G]GGGAGGATTGCTGGA | 51433 |
rs34868151 | in-del | -/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355422 | TTAGCCAGGCATGGT[-/G]GGGGGGTGCCTGTAA | 51433 |
rs35021667 | in-del | -/T | 0.448963 | 0.151372 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340733 | ATTTTTGTGTGTGTG[-/T]TTTTTTTTAGCAGAA | 51433 |
rs35055879 | in-del | -/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315654 | TGTTTTCTTTTTTTT[-/C]CTTTGATCAACTGGT | 51433 |
rs35114805 | in-del | -/CT | 0.0614824 | 0.164198 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316724 | GGTGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA | 51433 |
rs35252229 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318881 | AAAAATTAGCTGGGC[A/G]TAGTGGTGGGCACCT | 51433 |
rs35297026 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319117 | TGTGTATACACAAAC[-/A]CACACACACACACAC | 51433 |
rs35368013 | snp | A/G | 0.00192715 | 0.0309816 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335685 | TGTTGAACTGAAAAC[A/G]TCTTGGACACGGAGG | 51433 |
rs35481664 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340637 | CGCTCACCGCAACCT[C/T]CACCTCCCGGGTTCA | 51433 |
rs35572979 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313620 | ACAAGAATACCATGA[-/G]ACAATTCTATGCAAG | 51433 |
rs35625608 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334371 | GATGTCTCCATTATT[-/G]GAACTGTGAACACTA | 51433 |
rs35688561 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316762 | AAAAAAAAAAAGAAA[A/C]CAGGTGTTCAAACAA | 51433 |
rs35708047 | in-del | -/TT | 0.0599851 | 0.162463 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322648 | TGGTTATTTCTAATA[-/TT]TTCCATTTAAAAAAT | 51433 |
rs35718230 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339657 | GTGTTTTAATAGAGA[C/T]GGGGTTTCACCATGT | 51433 |
rs35742192 | in-del | -/AA | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310934 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 51433 |
rs35879072 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348418 | CCTATAATCCCAACA[-/T]TTTTGGGAGGCCAAG | 51433 |
rs35897335 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332083 | AGGCGATCCTCCTGC[-/T]CTCAGCCTCCCAAGT | 51433 |
rs35903379 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329687 | ATGGCACAATCTCGG[C/T]TCACTGCAATCTCCA | 51433 |
rs35933671 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309146 | GAGTGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs35989752 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316733 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51433 |
rs36095958 | snp | A/G | 0.00144423 | 0.0268334 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327120 | GTGTAGCTCTGCGAG[A/G]TGGCAGAGTGCGACA | 51433 |
rs36122756 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350005 | TGTGATCCCACCCGG[A/C]CTTTTATTTACCAAA | 51433 |
rs55794509 | snp | A/G | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121356048 | ACCTCCTGTGCTCAA[A/G]CGATCCTCCCACCTC | 51433 |
rs55955829 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323388 | GGAGTGTAGTGGTGC[A/G]ATCTCAGCTCATTGC | 51433 |
rs55971000 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323400 | TGCAATCTCAGCTCA[C/T]TGCAACCTCTACCTC | 51433 |
rs56126037 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323387 | TGGAGTGTAGTGGTG[C/T]AATCTCAGCTCATTG | 51433 |
rs56126551 | in-del | -/T | 0.42263 | 0.180829 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354003 | TTTTTTTTTTTTTTT[-/T]CCCGATACGGAGTCT | 51433 |
rs56332209 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314652 | TGAGAGGGAGTCTTG[A/C]TGTTGCCCAACCTGT | 51433 |
rs57825515 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322956 | CTTGAACCCAGGAGG[C/T]AGAGGTTGCAGTGAG | 51433 |
rs58008079 | in-del | -/AAG/AGA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315501 | GAAAAAGAACAAAGA[-/AAG/AGA]CTCCCACTTCCTGAT | 51433 |
rs58016198 | in-del | -/AA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344597 | AAAAAAAAAAAAAAA[-/AA]GAAAGAAAAAGAAAG | 51433 |
rs58510481 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344597 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAGAAAG | 51433 |
rs59155973 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321549 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 51433 |
rs59191226 | in-del | -/GAGA | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310259 | AAAAAAAAAGAGAGA[-/GAGA]ATTAAAATGGTACAC | 51433 |
rs59411698 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309168 | AAAAAAAAAAAAAAA[-/A]GGCCGGGCGCAGTGG | 51433 |
rs59997381 | snp | C/T | 0.175254 | 0.238565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338130 | TGTAATCCCAGCACT[C/T]TGGGAGGCAGAGGCT | 51433 |
rs60691023 | in-del | -/T | 0.365853 | 0.221536 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332577 | CAAGTTTTTTTTTTT[-/T]CTTTTTCACTGCTGT | 51433 |
rs60773958 | snp | A/G | 0.107341 | 0.205301 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345150 | ATCTGCTGAGGGACT[A/G]GGGTGAAGGACAGGG | 51433 |
rs60806586 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343167 | GAGTTAGACCTAAAT[A/T]AATCAAGTTAAGAGA | 51433 |
rs61151210 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339581 | GTTCAAGCGATTCTT[C/T]TGCTTCAGCCTCCCA | 51433 |
rs61516038 | in-del | -/TTTTG/TTTTGTTTTG/TTTTGTTTTGTTTTG | 0.528876 | 0.0908698 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353435 | ACTGTGCCTTGTGCC[lengthTooLong]TTTTGTTTTGTTTTG | 51433 |
rs61757696 | snp | A/T | 0.00787932 | 0.0622702 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121320403 | GGCGTGCTGACTATT[A/T]GGCGGAAATCGTTCC | 51433 |
rs61757697 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342006 | GAATTCACATACCTG[C/T]TGAGAAAGAAAAAAT | 51433 |
rs61955065 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354006 | TTTTTTTTTTTTTCC[C/T]GATACGGAGTCTTGC | 51433 |
rs62620751 | snp | C/T | 0.0581537 | 0.160297 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331462 | TTAATATCCCATTAA[C/T]AATCACAAACATGCA | 51433 |
rs66518635 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331852 | TATGTTTGTTTGTTT[-/G]TTTTTTAGAGACAGG | 51433 |
rs66834329 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325512 | TTAAAAATTAAAAAA[-/T]AAAAAAGAATTGAAC | 51433 |
rs71079053 | in-del | -/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321367 | TTTTTTTTTTTTTTT[-/T]ATGAGACAGGGTCTT | 51433 |
rs71079054 | in-del | -/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339869 | TTTTTTTTTTTTTTT[-/T]CCCAGATGGAGTGTC | 51433 |
rs71079055 | in-del | -/T/TT | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349736 | TTTTTTTTTTTTTTT[-/T/TT]GGAGACGGATGCCCA | 51433 |
rs71079056 | in-del | -/TTGTTGGTGGTGGTG | 0 | 0 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352720 | TGGTTGTTGTTGTTG[-/TTGTTGGTGGTGGTG]GTGGTGGTGGTGGTG | 51433 |
rs71305664 | in-del | -/AGA/GAA | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315502 | CTGAAAAAGAACAAA[-/AGA/GAA]GACTCCCACTTCCTG | 51433 |
rs71453553 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349039 | GGAGGCTGAAGCAGG[CA/TG]GATTACTTGAGGTCA | 51433 |
rs71454687 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338512 | GAGAATCACTTGAAC[C/T]CGGGAGGCAGAGATT | 51433 |
rs71454688 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338654 | TATGGGGAAAAATTA[C/T]TCCAAAAATATAGAA | 51433 |
rs71454689 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339560 | ACTGCAAACTCCGCC[C/T]CATGGGTTCAAGCGA | 51433 |
rs71454690 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339619 | GGGACGACAGGCACA[C/T]GCCACCACATCAGCT | 51433 |
rs71454691 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348936 | AGTTGAATTATGTTG[C/T]TTTTCTTACTGTGAA | 51433 |
rs71454692 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351538 | TCTCGGCTCACTGCA[A/G]CCTCCGCTTCCCAGG | 51433 |
rs71790112 | in-del | -/T | 0.393619 | 0.204631 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319238 | CTTATCTGTATTTTC[-/T]TTTTTTTTTTTTGGA | 51433 |
rs73405770 | snp | A/G | 0.124837 | 0.216412 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323054 | ACAAACAAACAAAAA[A/G]CCTTAGAAGTGGAAA | 51433 |
rs73405781 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344626 | AGTATTTGGGATAGG[C/T]GCTACCTCGTGGTCA | 51433 |
rs73405782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346296 | ATGGCTGTTACACTA[A/T]CTGAAATGATATTTA | 51433 |
rs74387348 | snp | C/T | 0.416218 | 0.186739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311496 | CAGTGTTCCAAAGCA[C/T]ATGAAGCAAAAACTG | 51433 |
rs74453755 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350696 | AAAAAAAAAAAAAAA[A/G]TCCTCTCCATGAGTG | 51433 |
rs74564432 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354047 | AGTCTGGAGTACAGT[A/C]GCTCGATTTCGGCTC | 51433 |
rs74644630 | snp | A/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310253 | ATGTTTAAAAAAAAA[A/G]GAGAGAATTAAAATG | 51433 |
rs74644631 | snp | G/T | 0.0477268 | 0.146926 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337408 | CTGAAATTTAAAAAT[G/T]GTAACTCAGTAGAAA | 51433 |
rs74679277 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318164 | GACTACCTTTCCAGA[C/T]GTCAATATGAACAAA | 51433 |
rs74728277 | snp | A/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351936 | TTGCAAAAAAAAAAA[A/T]TGCATGTAAAGCGCC | 51433 |
rs74786391 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310070 | AATATAGCAGGGGGC[A/G]GTTATTCACACTATG | 51433 |
rs74820648 | snp | A/G | 0.0158469 | 0.0875917 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308025 | ACAGGAACCACAAGC[A/G]CTGGTTCAGTCCAAC | 51433 |
rs75046962 | snp | G/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317269 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 51433 |
rs75088361 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315998 | CTAACAAGAAAGTGA[A/G]AAGACCAAACACAGA | 51433 |
rs75105144 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314457 | AATCAATCAATGCAG[A/G]AAAAAAAAATTTGAC | 51433 |
rs75133175 | snp | A/C/T | 3.36005e-05 | 0.00409867 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352177 | AGCCTCCGCCGCTCC[A/C/T]TGAGGCTGACGGCGC | 51433 |
rs75189734 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323718 | TTTTGTCTACATAGA[C/T]GCTCAGGCCACATGT | 51433 |
rs75261496 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313791 | GCCCAGGGCCAGACT[A/G]CTTCACTGGTGAATT | 51433 |
rs75354932 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351464 | CCTTGGCTTTATGCC[C/T]TTTTTTTTTTTGAAA | 51433 |
rs75416075 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316681 | GAGCTTGCAGTGAGC[C/G]GAGATTGCACCACTG | 51433 |
rs75463228 | snp | G/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340555 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 51433 |
rs75672629 | snp | A/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321342 | AAGAACAAACAAATT[A/T]CTTTTTTTTTTTTTT | 51433 |
rs75718536 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338160 | TGAGGCATGAGTATC[A/G]CTTGAGCCCAGGAGT | 51433 |
rs75734416 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322586 | TCGTAGTATTTTATC[A/G]GGAAAATCAATTATG | 51433 |
rs75918756 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335790 | TAAGACAACTGCAGA[C/G]AGTTCCACTGTCTAC | 51433 |
rs76232928 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314456 | AAATCAATCAATGCA[A/G]AAAAAAAAAATTTGA | 51433 |
rs76282096 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327989 | TCAGATGACGTGGGT[C/T]TGAGTCCTTTCTCTG | 51433 |
rs76296260 | snp | G/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349736 | TTTTTTTTTTTTTTT[G/T]GGAGACGGATGCCCA | 51433 |
rs76804421 | snp | G/T | | | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352269 | CCAGTCCTTGATGCC[G/T]AACACATTGGCGTGC | 51433 |
rs76947285 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310252 | TATGTTTAAAAAAAA[A/G]AGAGAGAATTAAAAT | 51433 |
rs77102996 | snp | G/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329633 | TTTTTTTTTTTTTTT[G/T]AGATGGAATTTCATT | 51433 |
rs77154669 | snp | A/G | 0.147991 | 0.228242 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322671 | TTAAAAAATGCTACA[A/G]TGAATATCTTGGTGC | 51433 |
rs77176335 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343998 | GATAACAGTAGTTAG[A/G]GAAGGAGAAGTAAAA | 51433 |
rs77267993 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351462 | GTCCTTGGCTTTATG[C/G/T]CTTTTTTTTTTTTGA | 51433 |
rs77543176 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329465 | CCGATTTTAAAGTGT[A/C]TACATTAAATTACTA | 51433 |
rs77636759 | snp | A/C | | | missense | ANAPC5 | GRCh38.p7 | 12:121319805 | TGTATTTTTTGATCA[A/C]ATAGCATCCATAACT | 51433 |
rs77643638 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340302 | GCCTGGGCAACAAAA[A/G]CAAAACTCCATCTCA | 51433 |
rs77665338 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322585 | ATCGTAGTATTTTAT[C/T]GGGAAAATCAATTAT | 51433 |
rs77789874 | snp | A/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312732 | AAAAAAAAAAAAAAT[A/T]ACCCTAGTGTGGTGG | 51433 |
rs77796854 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350697 | AAAAAAAAAAAAAAA[G/T]CCTCTCCATGAGTGC | 51433 |
rs77885487 | snp | C/T | 0.0010054 | 0.0223984 | missense | ANAPC5 | GRCh38.p7 | 12:121309765 | CTTGGCCACTAAGAA[C/T]ATGGCACGACCTTTG | 51433 |
rs78010053 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348264 | CAAAGTGCTTTGTAA[A/G]CTGGAAAACACTATA | 51433 |
rs78031662 | snp | A/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319032 | CTCAAAAAAAAAAAA[A/T]GTTTTTGTTGTTGAA | 51433 |
rs78035279 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352539 | CCCTCCCCGCACTCT[A/T]GTACATTCTGACTGG | 51433 |
rs78242344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329016 | TCAACTAAAAAATGC[C/T]AGCTTAAATTCATGG | 51433 |
rs78279975 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337581 | GGACCCTGCCACATG[A/C]TCTCCTCTTGACCAT | 51433 |
rs78358876 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349273 | GATTAAAACTATACA[A/G]TAGGGGGCCAGGTGT | 51433 |
rs78375200 | snp | G/T | 0.113513 | 0.211231 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348999 | GCCTGGCGCAGTGGC[G/T]CACGCCTGTAATACC | 51433 |
rs78376526 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321249 | AACAAAATTCCGTCT[A/C]AAAAAAAAAAATTTT | 51433 |
rs78411593 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319644 | TATAAAACAAAAACA[A/C]AACCATTTAACAATT | 51433 |
rs78488548 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317718 | TAATGTACAGCCAGT[C/T]TGGAGAACCTCCACT | 51433 |
rs78763063 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341588 | TGGTGGCTGAATAGA[C/G]AGTGGTTAGATAAGT | 51433 |
rs78982107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337906 | AGTGCCTGTATGGGG[C/T]CTTATGGGAGCCAGG | 51433 |
rs78983215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317692 | TATTTTTTAAATCTC[C/T]GCAATAATTCTAATG | 51433 |
rs78999191 | snp | A/C/T | 0.0228417 | 0.1044 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331454 | ACTAAACATTAATAT[A/C/T]CCATTAATAATCACA | 51433 |
rs79105156 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344184 | ACAGAGAAGGGTCTC[A/G]GTTCTCAAGGGGTGA | 51433 |
rs79378079 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321250 | ACAAAATTCCGTCTC[A/C]AAAAAAAAAATTTTT | 51433 |
rs79387984 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331945 | TTCCTGGACTCAGGC[A/G]ATGGACCTCAGCCTC | 51433 |
rs79486147 | snp | A/G | 0.0617778 | 0.164537 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308739 | AACTCAACCCTTCAC[A/G]TATAGTTTTCAAAAC | 51433 |
rs79487416 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315745 | AGAATAACCTATATC[C/T]GTATGCAGAAGAATA | 51433 |
rs79531715 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320559 | CCTGTTCCCGTTCTT[C/G]ATGCAGCAACCTGAG | 51433 |
rs79880512 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336694 | TCCAAAACAAACAAA[A/C]AAACACTGTTTTTTG | 51433 |
rs79909096 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348761 | AAAACTAAATTTAGA[A/C]TCTTTTTCAGAGAAT | 51433 |
rs79980248 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310250 | AGTATGTTTAAAAAA[A/G]AAAGAGAGAATTAAA | 51433 |
rs80103231 | snp | C/T | 0.115438 | 0.210697 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333829 | TTCACTACATGAAGA[C/T]GTCAAACACATGCTT | 51433 |
rs80124621 | snp | G/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327515 | TGTTCCCTGCAGTCA[G/T]AGTATGTTAATTAGT | 51433 |
rs80199434 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316128 | AGTTAAAAAACAGGT[A/G]AAGGATCGGAATAGA | 51433 |
rs111285880 | in-del | -/C | 0.132751 | 0.2208 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334987 | TTTTCATAAACTGTT[-/C]CAGTGCCAATAAGGT | 51433 |
rs111320099 | snp | C/T | 0.0184072 | 0.0941529 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309714 | ACCTTCTGCTTTCTT[C/T]GGCTGATCGTAGGAA | 51433 |
rs111559847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318062 | CTTACTGAATACACA[A/G]CTCAGGAAAGCCAGT | 51433 |
rs111582580 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337089 | TGGGCGTGGTGGCAC[A/G]TGCCTGTAATCCCAG | 51433 |
rs111640641 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350210 | AGTGATAAATTTTTT[A/T]AAAAAGCCTTTATAA | 51433 |
rs111724696 | snp | A/C/T | 8.98119e-05 | 0.0067007 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318280 | AGATCGGCTTACCTG[A/C/T]GCAAAAGCCAAGTTC | 51433 |
rs111753112 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346431 | AGAGAAATAGCTCAC[A/G]CTGAATAACATAAAA | 51433 |
rs111759075 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334568 | GATAGCCTCCATGTT[C/T]TGAAAGTTGTTTTAT | 51433 |
rs111791371 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346044 | AACCTACAAAATAAG[A/G]CGAGAGACAAGGGGA | 51433 |
rs111876015 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347170 | CAAAATGTTACTCCC[A/G]TATTTCTGAAAAGTA | 51433 |
rs111940471 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308034 | ACAAGCGCTGGTTCA[C/G]TCCAACAAGGCAGGG | 51433 |
rs111961078 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345919 | CATATCAGCATCCTC[C/T]ACTGTCTTTTTCTCA | 51433 |
rs112035973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342481 | CCAAAAACCGTAAAA[C/G]TCTTAGAAGATCTTC | 51433 |
rs112043055 | snp | G/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323816 | ATTTTAACTGGCCAG[G/T]CTCACCAATTATTTT | 51433 |
rs112059041 | snp | C/T | 0.287085 | 0.247234 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321047 | CTGAGGTTGGGAGTT[C/T]GAGACCAGCCTGACC | 51433 |
rs112065851 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320630 | TTTTTTTGGGACAGA[G/T]TCTCGCTCTGTAGCC | 51433 |
rs112121884 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311182 | GGAGGATCCCATCAG[C/T]CCAGGAGTTCAAGGT | 51433 |
rs112131951 | snp | A/G | 0.174288 | 0.23826 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318747 | TGAAAGAGGCTGAGC[A/G]CGGTGGCTCACACCT | 51433 |
rs112149286 | in-del | -/A | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325506 | TAAAAATTAAAAATT[-/A]AAAAAAAAAAAAGAA | 51433 |
rs112248993 | snp | A/C | 0.182933 | 0.240836 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310761 | CAACATGGTGAAACC[A/C]TGTCTTTCCTAAAAA | 51433 |
rs112285776 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322044 | CTAATATTTGTATTT[C/T]TAGGAGAGACAGGGT | 51433 |
rs112305467 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338739 | TATTAATACTTTAGT[A/G]TATATTATCCTAGTC | 51433 |
rs112358864 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121356193 | CTCACAAAATCCTCC[C/T]ACCTCAGTCTCCCAA | 51433 |
rs112408010 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325512 | ATTAAAAATTAAAAA[A/T]AAAAAAGAATTGAAC | 51433 |
rs112447102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342697 | AAACCTGTCTCTACT[A/G]AAATACAAAAAATTA | 51433 |
rs112450644 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331440 | TTGACTAATGACAGA[C/T]TAAACATTAATATCC | 51433 |
rs112455670 | snp | G/T | 0.14933 | 0.228835 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325810 | AGGCAGAGGTTGCAG[G/T]GAGCTGAGATCGTGC | 51433 |
rs112534314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346824 | GATATAGCAGAACAA[C/T]GATAGACATGACTTA | 51433 |
rs112537090 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312285 | ACCACAGACTCTGGC[C/T]GGGCGCAGTGGCTCA | 51433 |
rs112607932 | snp | C/T | 0.108402 | 0.206034 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354339 | AGACACGAGGTCTTG[C/T]GATGTTGTCCAGGCT | 51433 |
rs112617629 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317010 | CACATTTATATGAGT[C/T]CAGTTATGCAAACTG | 51433 |
rs112773762 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333411 | GGAAGCAGTTCCTTA[C/G]TAAGTTAAATAGGTT | 51433 |
rs112795038 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339312 | TGCCTCTGCCTCCCA[A/C]AGTGCTGGGATTATA | 51433 |
rs112808731 | snp | A/G | 1.72791e-05 | 0.00293926 | missense | ANAPC5 | GRCh38.p7 | 12:121318327 | CCAAGTACTGTAACC[A/G]GTACTCCTTGGAGAG | 51433 |
rs112831315 | in-del | -/A | 0.168785 | 0.236441 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339514 | CTCGCTCTGTCGCAC[-/A]AGCTGAAGTACAGTG | 51433 |
rs112857720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336230 | TACTAGGAAGCAAAA[C/T]AGATATATTTCTGCA | 51433 |
rs112946054 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331326 | GTGAACAAAACTCCC[A/G]AGACCAGAGGATGGC | 51433 |
rs113012479 | snp | A/C | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349164 | CCAAAGTCTAGGCAC[A/C]AAGCCAAAAATTAAC | 51433 |
rs113016079 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338017 | CAAATTAAATGTTTA[C/T]ATTTAACTGGGTTAT | 51433 |
rs113066454 | snp | A/G | 0.14665 | 0.227637 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321853 | GACAAATTACTTTTG[A/G]GTTTTGCTGTTGTTG | 51433 |
rs113088151 | snp | C/T | 0.116838 | 0.211584 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310900 | GATCACACCACTGCA[C/T]TCCAGCCTGGGTGAC | 51433 |
rs113097134 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340645 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 51433 |
rs113139253 | snp | C/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330819 | ATCAAGAATCTCAAT[C/G]AGACCTGTCAAACAT | 51433 |
rs113154299 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310251 | GTATGTTTAAAAAAA[A/G]AAGAGAGAATTAAAA | 51433 |
rs113179471 | in-del | -/AGAG | 0.499968 | 0.00399348 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310252 | ATGTTTAAAAAAAAA[-/AGAG]AGAGAGAATTAAAAT | 51433 |
rs113180621 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346825 | ATATAGCAGAACAAT[A/G]ATAGACATGACTTAG | 51433 |
rs113205214 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327845 | AAACACCTCAGTTAA[C/G]AGAAAAGCAACTTTC | 51433 |
rs113262962 | in-del | -/A | 0.416218 | 0.186739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311490 | AAACAACAGTGTTCC[-/A]AAGCATATGAAGCAA | 51433 |
rs113276803 | snp | A/C/G/T | 0.00021392 | 0.0103401 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352107 | AAAAGTTTGCTGCAC[A/C/G/T]AGCAGGAGCCAGCGG | 51433 |
rs113277875 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344307 | TTTGGGGCCGAGTGC[A/G]GTGGCTCACGCCTGT | 51433 |
rs113363039 | snp | C/T | 0.5 | 0 | missense | ANAPC5 | GRCh38.p7 | 12:121318568 | GTAAAAGCTTATGTG[C/T]CTCTGACATTTGGTT | 51433 |
rs113500678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311985 | CCTAACATATATATA[C/T]AAAGCATGCCACCCA | 51433 |
rs113639033 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331005 | GTGTTCCACTGCCCT[A/G]GTGATTTTGCTATTA | 51433 |
rs113695704 | snp | C/G/T | 0 | 0 | splice-donor-variant, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331346 | CAGAGGATGGCCTCA[C/G/T]CAAACAGTGCTGGAG | 51433 |
rs113720618 | snp | A/C/T | 0.000139703 | 0.00835672 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335506 | GGTTCCTTCAATTTG[A/C/T]GCAAGGACAAAGGTC | 51433 |
rs113743250 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341872 | GGCAGAGGGGACCAA[A/G]AGTAAAGGCTGACAC | 51433 |
rs113776729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308847 | AACCACTAGGGTGAG[A/G]TTTTCAAAAAGGTCT | 51433 |
rs113780227 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323441 | GCAATCCTCCCACCT[C/T]AGCCTCCCTAGTAGC | 51433 |
rs113828403 | snp | A/C/T | 0.00113634 | 0.0238096 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346084 | CTGACATCCAGGCTA[A/C/T]GCAATGGCAACTCCA | 51433 |
rs114147962 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345874 | TTCTTTTTCCATTTT[C/T]CTTTCACCCTCATCT | 51433 |
rs114172811 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324124 | GCACCATCCAATTTA[C/T]TTGAAGGAAAGTTTC | 51433 |
rs114213300 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346583 | CTCTTCATAAGTCTG[A/G]GCTGGTGACCCTCAC | 51433 |
rs114248389 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351706 | TCGTGATCCACCCGC[C/T]TTACCCTCCCAAAGT | 51433 |
rs114313098 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327472 | CAGCTGGGAGTACAC[A/G]CTCCCAGATCCCCCC | 51433 |
rs114334895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345095 | GGCTATGAGATAAGT[A/G]AACAAGTTCCAAACA | 51433 |
rs114339751 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342157 | ATGGATTCTTGTATC[A/G]AAAGAGTTCAAAAAA | 51433 |
rs114367016 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334507 | GATCTTTGAATTAGT[A/G]ATTTCCCACCTTTCA | 51433 |
rs114514914 | snp | A/G | 0.113334 | 0.209338 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341198 | AAATGTTTGGGGCAC[A/G]CTGGTTCATGTCTGT | 51433 |
rs114517123 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348684 | AAAAAAAAAAGAGTA[C/T]CACAAGGAATAAAGA | 51433 |
rs114544541 | snp | A/G | 0.000371108 | 0.0136168 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318373 | GAGCATGGGCAGCGC[A/G]ATGGTAGGGGAGGAA | 51433 |
rs114577558 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334909 | GAAGTAATGAAAGAG[A/G]CTAGGCACTAAGACG | 51433 |
rs114635317 | snp | C/T | 0.00021458 | 0.0103559 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330608 | AAATGTACTGCCTTC[C/T]TCACAGAATGCTCCA | 51433 |
rs114730469 | snp | A/G | 0.000463883 | 0.0152226 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327132 | GAGGTGGCAGAGTGC[A/G]ACAGCAAAGGACTCT | 51433 |
rs114820787 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320309 | TTTTCTGAGGGGAGA[C/T]TATGTCCCACTTTAT | 51433 |
rs114872735 | snp | A/G | 0.00307583 | 0.0390954 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308603 | GAGTCTGGCCTGGAA[A/G]TAAACGACGTCCCTG | 51433 |
rs114915570 | snp | A/G | 0.000399281 | 0.0141238 | missense | ANAPC5 | GRCh38.p7 | 12:121320389 | AGGCAGATTACCTGG[A/G]CGTGCTGACTATTAG | 51433 |
rs115146269 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338244 | ATTTCTTTAAAAAAA[A/T]TTTTTTTAAAGTAAA | 51433 |
rs115171904 | snp | C/T | 0.00146884 | 0.0270604 | missense | ANAPC5 | GRCh38.p7 | 12:121319772 | TGATATTTGCCATCA[C/T]TCATTGCTCTGTCAA | 51433 |
rs115307933 | snp | C/T | 0.00139606 | 0.0263834 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351154 | GACGGGAGGATTGCT[C/T]GAGTCCAGGAGTTCC | 51433 |
rs115319479 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325978 | GAGGTGCCAGTGCCA[C/T]GAAGAGGGAAGAAAC | 51433 |
rs115493583 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327952 | GTTCCTGTCACAGAG[A/C]AGAGGAGCCCGGTGC | 51433 |
rs115614545 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310602 | TTAACACACAAGAAA[A/G]CAGTAATGGAGGAAC | 51433 |
rs115738542 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349576 | CACTCTAAAAAAATT[A/T]AAAAAAAAATAAATT | 51433 |
rs115741634 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342979 | TAATTTCTTTTAGAC[A/G]AAGAATTATAATCAT | 51433 |
rs115750764 | snp | A/G | 0.00105615 | 0.0229556 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318412 | GTACAGCTCTGCCAC[A/G]GACAGTAGGACACTG | 51433 |
rs115883214 | snp | A/G | 0.00289516 | 0.0379368 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308612 | CTGGAAGTAAACGAC[A/G]TCCCTGATGCGCTCT | 51433 |
rs115934510 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | ANAPC5 | GRCh38.p7 | 12:121308547 | TGCCGGAAGAGCATC[A/G]CACACCGGTTCCTCT | 51433 |
rs115939291 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344980 | CCTGAAGAACAGATG[C/T]AGGGAGACAGGAGTT | 51433 |
rs116010790 | snp | G/T | 0.209135 | 0.246638 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352721 | TGGTTGTTGTTGTTG[G/T]TGGTGGTGGTGGTGG | 51433 |
rs116012709 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327441 | CAGCGCGAGGAGACA[C/G]GTAGTGGTTAGGGCA | 51433 |
rs116050005 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328716 | GTACACGGGAAAGAG[C/T]CAGCAGGGCTTTAGC | 51433 |
rs116135448 | snp | C/T | 0.00930212 | 0.0675613 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330632 | TGCTCCAGCAGAACA[C/T]AGCTATCGGATCTCT | 51433 |
rs116190468 | snp | A/C/T | 0.0185938 | 0.0946107 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349851 | AGCTGGGACTACAGG[A/C/T]GCACATCACAATGCC | 51433 |
rs116227311 | snp | C/T | 6.61529e-05 | 0.00575083 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327168 | GTTCTGCTGCACGCC[C/T]GCATTCACCGCCTCC | 51433 |
rs116306489 | snp | C/G | 0.00115869 | 0.0240417 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352221 | GCTCATCTCGTTCAG[C/G]AGCACCAGCACCGCG | 51433 |
rs116437533 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332996 | CTATATTTTTAAAAA[C/T]AAAAAGAAGAAATTC | 51433 |
rs116523210 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327297 | GCTTTGGCCATGCCC[A/G]TCAGCTATCTTGAGT | 51433 |
rs116560122 | snp | A/G | 0.00188728 | 0.0306607 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318431 | AGTAGGACACTGACC[A/G]TAAAGAGGAAAACAC | 51433 |
rs116573315 | snp | C/T | 0.0183063 | 0.0939044 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308534 | CTCCTGATGCAGCTG[C/T]CGGAAGAGCATCGCA | 51433 |
rs116640700 | snp | A/C/T | 0.000237173 | 0.0108873 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309654 | GTCCTAAACTTTCAA[A/C/T]GCTTTCTGGAATAGC | 51433 |
rs116707883 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340181 | AAATTAGGCAGCTGT[A/G]GTGGCAGGCACCTCT | 51433 |
rs116961756 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343686 | TACAAAAACTACTCA[A/T]AGAAAGTGCGATAAG | 51433 |
rs117071358 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344306 | ATTTGGGGCCGAGTG[C/T]GGTGGCTCACGCCTG | 51433 |
rs117172105 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314247 | TCTACTAAAATACAA[A/C]AATTACTTGGGCATG | 51433 |
rs117440392 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340997 | ATGTTCAGATTATGT[G/T]TCCAAGAAAATGAAA | 51433 |
rs117452140 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350003 | GGTGTGATCCCACCC[A/G]GCCTTTTATTTACCA | 51433 |
rs117512370 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324845 | TATGATTGTGCCACC[A/G]CACTCCATCCTGGGC | 51433 |
rs117562882 | snp | G/T | 0.0185938 | 0.0946107 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308172 | TTACATAATGATGGA[G/T]TGTGTACAATTTCTA | 51433 |
rs117651104 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338662 | AAAATTATTCCAAAA[A/G]TATAGAAAACCTACA | 51433 |
rs117683496 | snp | C/G | 9.91965e-05 | 0.0070419 | intron-variant, stop-gained, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352242 | CAGCACCGCGATCTT[C/G]TACGGCGTCACCCAG | 51433 |
rs117963325 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323392 | TGTAGTGGTGCAATC[C/T]CAGCTCATTGCAACC | 51433 |
rs118133543 | snp | C/T | 0.077417 | 0.180873 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334219 | ATGAGTTTGAGGTTA[C/T]AGTTAGCTATGATCA | 51433 |
rs118176996 | snp | A/G | 0.0182358 | 0.0937301 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318255 | GCACAAATATGTGCT[A/G]TAAAAACAGAGATCG | 51433 |
rs137972372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341406 | ACCCAGGAGGCAGAG[A/G]TAGCAGGGACCCGAG | 51433 |
rs138103467 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335644 | CCGGTAAGAATCAGA[C/T]GATCAAAATAATGGA | 51433 |
rs138123190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332343 | TGTTCAAATATTAAG[C/T]TGGCAGAGATCAAGG | 51433 |
rs138134307 | snp | G/T | 0.000159437 | 0.00892711 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318301 | AGCCAAGTTCAGCAC[G/T]GTTTCAGAGGCCAAG | 51433 |
rs138175231 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354114 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAACTAC | 51433 |
rs138182382 | snp | C/T | 0.00528208 | 0.0511189 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320479 | AGTAGAAACACACAA[C/T]TTGATCAGCATAACC | 51433 |
rs138201522 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337209 | GCAACAGAGTAAGAC[G/T]CTGTTTCCAAAAACA | 51433 |
rs138226513 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324327 | CTAGAAAGATCTAAG[G/T]CAAGATGAAGAAAGG | 51433 |
rs138273182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319319 | CTCACTGCAACCTCC[A/G]CCTCATGGGTTCAAG | 51433 |
rs138276234 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348308 | TCACAAACACAATCT[A/C]ATTTGATCTTCTCCC | 51433 |
rs138450820 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315494 | AAAACAATCCTGAAA[A/G]AGAACAAAGACTCCC | 51433 |
rs138513974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341722 | TAAAATGTTGAGAGA[A/C]GGGTTAAATCACAGG | 51433 |
rs138532723 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344624 | AAAGTATTTGGGATA[A/G]GCGCTACCTCGTGGT | 51433 |
rs138537425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351703 | ACCTCGTGATCCACC[C/T]GCCTTACCCTCCCAA | 51433 |
rs138614006 | snp | C/T | 8.2498e-05 | 0.00642201 | missense | ANAPC5 | GRCh38.p7 | 12:121309794 | TGTCCAGGATAGCCC[C/T]GTCAGCCAAGATGGG | 51433 |
rs138745992 | snp | C/T | 1.67298e-05 | 0.00289217 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346995 | ACTCGCCTTCAGCCA[C/T]CAGTTTGATTCTGAA | 51433 |
rs138789548 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337939 | GCTTGCCCCAGCTCT[A/C]CTTATTTGTTTCATA | 51433 |
rs138838921 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323320 | ATACTCTTATATTGT[C/T]GGGATGTTTATCTTT | 51433 |
rs138931971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344997 | GGGAGACAGGAGTTA[A/G]GTCAAGGAGAAAAGT | 51433 |
rs139005234 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334479 | AGCCACAGGGCAGGT[C/G]GGGGGGTGAAGGGAT | 51433 |
rs139133202 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328139 | AACATGCATGGGAAA[A/G]AAGTTTTCAGTCTGT | 51433 |
rs139209777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346542 | TCACTTTGCATACTA[C/T]ATCAATAATGTATTT | 51433 |
rs139227556 | in-del | -/AAG | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342245 | TGCACAGAGCCCATA[-/AAG]AAGCCCTGGCATGCA | 51433 |
rs139255677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310130 | AGCATTAATATCCTT[C/T]AGCTTGGTGATTCTG | 51433 |
rs139298522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342521 | GCTAGTAATAAAAAA[C/T]AAATAATACATTTTT | 51433 |
rs139334549 | snp | A/G | 0.000444865 | 0.0149075 | missense | ANAPC5 | GRCh38.p7 | 12:121320407 | TGCTGACTATTAGGC[A/G]GAAATCGTTCCTTCA | 51433 |
rs139346128 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312255 | ATTAGAAAATGCAAT[A/G]AGGTGTATAAAAATA | 51433 |
rs139347356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314552 | CCTCTATAAAAAACC[C/T]ACAGCTAGCATGATA | 51433 |
rs139384208 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317549 | GAGCCACCACACCTG[A/G]CCATGTACATTTTAT | 51433 |
rs139439499 | snp | C/T | 1.65225e-05 | 0.00287419 | intron-variant, synonymous-codon, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352284 | GAACACATTGGCGTG[C/T]ACAACCCCATTGGTC | 51433 |
rs139696351 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316192 | AAGCACATGAAAAGA[C/T]ACTCAACATCATTAG | 51433 |
rs139751384 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338945 | TTATATAATGTGTAT[A/G]TACACATTATATTTT | 51433 |
rs139963308 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354683 | GGAGAAGCTGGCTTT[G/T]GCCAGGAATTTAATA | 51433 |
rs140117497 | in-del | -/AGAG | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310253 | TGTTTAAAAAAAAAA[-/AGAG]GAGAGAATTAAAATG | 51433 |
rs140166955 | in-del | -/T | 0.215747 | 0.247642 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325511 | ATTAAAAATTAAAAA[-/T]AAAAAAAGAATTGAA | 51433 |
rs140248928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347265 | ATCTGCAATGACTAA[A/G]AAGAGTAAGATGGAT | 51433 |
rs140257918 | snp | A/G | 4.94939e-05 | 0.00497439 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335577 | AAGATTCAGAGCGGC[A/G]TATCTCAAGCTCCGG | 51433 |
rs140292131 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322165 | ACCGCACCTGGCCTG[-/T]GTTTTTTTTTTTGAG | 51433 |
rs140305746 | in-del | -/AA | 0.287606 | 0.247155 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319113 | ATGCTGTGTATACAC[-/AA]ACACACACACACACA | 51433 |
rs140315759 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307991 | CCAGTCAGGGACCAA[C/T]AAGTCCTCGTGAGCA | 51433 |
rs140338670 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329192 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 51433 |
rs140377052 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333544 | AGTTATTACAAGATA[C/T]CATGGAATGTTGCAA | 51433 |
rs140423985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337134 | GAGGCAGGAGAATCA[C/G]TTGAACCAGGGAGTC | 51433 |
rs140617768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323468 | TAGCTGGAACTACAG[A/G]CATGTGCCACCACAC | 51433 |
rs140643683 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330408 | ACAGAGAGAAACCTA[C/T]CACACAGAATTTAGT | 51433 |
rs140753558 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346364 | GTAATCTCCATAAGA[A/G]GAAATTCCATGTCTA | 51433 |
rs140767578 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313012 | ATCTCAAATCAATAA[A/G]CGAATCTTCCACCTT | 51433 |
rs140788777 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344215 | AGAGGCAGGGGAAAC[A/G]GATAAGCAAGCAAGC | 51433 |
rs140792985 | snp | A/G | 0.000725881 | 0.0190372 | missense | ANAPC5 | GRCh38.p7 | 12:121309730 | GGCTGATCGTAGGAA[A/G]CTGCTGAAGCCACCT | 51433 |
rs140857252 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333691 | AGAGGGTTCAATAAG[-/G]GGGAAACTGTTTCCT | 51433 |
rs141004861 | snp | C/T | 0.000182577 | 0.00955276 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352209 | CTCGCCTGTGCGGCT[C/T]ATCTCGTTCAGCAGC | 51433 |
rs141045075 | snp | A/G | 0.000148838 | 0.00862536 | missense | ANAPC5 | GRCh38.p7 | 12:121327184 | GCATTCACCGCCTCC[A/G]GGCTGTTCATGCTCA | 51433 |
rs141069279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322893 | AGCCGGGCGCAGTGG[C/T]AGGTGCCTGTAATCC | 51433 |
rs141167213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333723 | ATAATGAGCAGAAAT[A/C]TTTTGTCCTTTAACC | 51433 |
rs141256427 | in-del | -/TA | 0.0130921 | 0.0798413 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338772 | TGTTCTGTATGTGTG[-/TA]TATATGTTACATATC | 51433 |
rs141278522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327665 | AAAAACAAGACTGGT[A/G]AAAAAGGCACTTCCT | 51433 |
rs141306512 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336218 | GCAGATCTCAGTTAC[C/T]AGGAAGCAAAATAGA | 51433 |
rs141486437 | snp | A/G | 0.0034421 | 0.0413425 | missense | ANAPC5 | GRCh38.p7 | 12:121318603 | GCTTGTAATACAACC[A/G]CTTTCCTGAAACAGA | 51433 |
rs141586075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348046 | AGTAATACTTCACAT[C/T]TGCATACCATTTTTG | 51433 |
rs141628719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338784 | GTGTATATATGTTAC[A/G]TATCATATTCTGATT | 51433 |
rs141875634 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319295 | CTGGAGGCAATGGTG[C/T]GATCTTGGCTCACTG | 51433 |
rs141903243 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315752 | CCTATATCCGTATGC[A/T]GAAGAATAAGAGTGG | 51433 |
rs141913815 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322379 | GGTCAGTCTGGTCTC[C/T]AACTCCTGACCTCAG | 51433 |
rs141981839 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320228 | AGCCTGTGTTTTTAA[A/G]CTTTATATAAATAAT | 51433 |
rs142119690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317985 | TTGCTAAATCAAGCA[A/T]CACTCTGTGTCAGCT | 51433 |
rs142136830 | snp | C/T | 3.31625e-05 | 0.00407188 | synonymous-codon, intron-variant | ANAPC5 | GRCh38.p7 | 12:121331401 | GGCAATCCTAATTGC[C/T]TCCTGCAGGGCGAGC | 51433 |
rs142220645 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308840 | AAAACAAACCACTAG[-/G]GGTGAGGTTTTCAAA | 51433 |
rs142221483 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312077 | TGTTTGGGCCACAAA[A/G]TAACACTCAATAAAT | 51433 |
rs142286810 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340243 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 51433 |
rs142401708 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342273 | ATGCATGGTCAAATG[C/G]TTTTTGGCAACAGTG | 51433 |
rs142566618 | snp | C/T | 0.0752113 | 0.178743 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355884 | AATAAGCCACCTTTA[C/T]TTAGGGCATGCCGTT | 51433 |
rs142669319 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320662 | TGCTGGAGTGCAGTG[G/T]CGCGATCTCGGCTCA | 51433 |
rs142727611 | snp | C/T | 0.000153988 | 0.00877328 | missense | ANAPC5 | GRCh38.p7 | 12:121318336 | GTAACCGGTACTCCT[C/T]GGAGAGGGCCAGAGC | 51433 |
rs143014110 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309313 | GCCAGTCTTGGTGGT[A/G]TGCGCCTTTACATAT | 51433 |
rs143064498 | snp | A/T | 0.030278 | 0.119257 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341898 | GACACAGACTGACCA[A/T]CAAACCTATGCACAT | 51433 |
rs143075711 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349002 | TGGCGCAGTGGCTCA[C/T]GCCTGTAATACCAGC | 51433 |
rs143099018 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332201 | CTCCTGGCCTCAAGC[A/G]ATCCTCCTTCTTTGG | 51433 |
rs143105051 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334479 | GCCACAGGGCAGGTG[-/G]GGGGGGTGAAGGGAT | 51433 |
rs143113420 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353780 | TTTAAATTATACTTT[A/C]TCTCTCTCTCATTCT | 51433 |
rs143202096 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310463 | AGTTACTCAGGAGGC[C/T]GAGGCAGGAGAATCA | 51433 |
rs143243261 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315106 | CCAAAACCTGTTACA[C/G]GTAATAAGTTTGGCA | 51433 |
rs143310882 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319509 | AAAGTGCTGGGATTA[C/T]AGGTGTAAGTCACCA | 51433 |
rs143351072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350409 | TCCTCGGGCCGGGCG[C/T]GGTGGCTCATGCCTG | 51433 |
rs143445758 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355666 | GGAGTTTGACACATG[C/T]CTGGCCAACATGGTG | 51433 |
rs143544201 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343716 | GCATTCCCCATTTAT[A/G]AACAATGTCACCCCC | 51433 |
rs143579319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332288 | TTTAGAAAGTATTTT[C/G]AGGATTCCCACTTCT | 51433 |
rs143656269 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337218 | TAAGACTCTGTTTCC[A/C]AAAACAAACAAACAA | 51433 |
rs143914138 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346171 | TTGCAGTTGCCATTC[C/T]CTCCTCCTGGAATGT | 51433 |
rs143981188 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348549 | ACACACCTGTAGTCC[C/T]AGCTACTTGGGAGGC | 51433 |
rs144031139 | snp | A/T | 0.0271762 | 0.113356 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352455 | TATCCCAGGAAACAG[A/T]CATCCGCGTGCTCGC | 51433 |
rs144114201 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317644 | TAGAGATTCTGACTC[C/T]GTAGGTCTGAGGCAA | 51433 |
rs144195789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326326 | AGAGAAAAATATGAT[C/G]AAGGAAACATCTGGA | 51433 |
rs144242008 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311441 | TACTCATGAAACAGT[C/G]GATTCATCAAGATAT | 51433 |
rs144370647 | in-del | -/AC | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319115 | GCTGTGTATACACAA[-/AC]ACACACACACACACA | 51433 |
rs144381309 | snp | A/C/T | 0.000214337 | 0.0103501 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335755 | TCAATGTATTTTAAA[A/C/T]GCTGTAAATATCTCT | 51433 |
rs144469445 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338370 | CGAGGAGGGCAGATC[A/G]TGAGGTCAGGAGTTG | 51433 |
rs144510826 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321245 | CAAGAACAAAATTCC[A/G]TCTCAAAAAAAAAAA | 51433 |
rs144599157 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346480 | CAGAGGGATAGAGCA[C/T]GGGATAAAGCTAATA | 51433 |
rs144633905 | snp | A/C/G | 0.0346267 | 0.127524 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344388 | ATTTGAGACCAGCCT[A/C/G]GCCAACACAGTGAAA | 51433 |
rs144692103 | snp | G/T | 0.030278 | 0.119257 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349324 | CCAGCACTTTGGGAA[G/T]CTGAGGCAGGTGGAT | 51433 |
rs144710413 | snp | A/G | 3.41997e-05 | 0.00413506 | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352139 | CGCCTCTCACCTGCA[A/G]CAGGGGCAGGAGCAG | 51433 |
rs144716812 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347094 | TACCTCAAATAATGT[A/T]TTTTACAGGCAATTC | 51433 |
rs144794447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345436 | AGTCATAAGACACAA[C/T]ACAGTCCCCAGGACT | 51433 |
rs144892909 | snp | C/T | 0.00144404 | 0.0268316 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351067 | AGCTAAACCTGTGTC[C/T]GCAAAATGAAATAAC | 51433 |
rs144912201 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328387 | CTCTGACAGGCTGTG[C/T]TTCCAGTGCAGGAGG | 51433 |
rs144967528 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312730 | AAAAAAAAAAAAAAA[-/A]TTACCCTAGTGTGGT | 51433 |
rs144971466 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345910 | GGTCAGTTCCATATC[A/G]GCATCCTCCACTGTC | 51433 |
rs145007196 | snp | A/C | 4.95217e-05 | 0.00497578 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328327 | CTACCTGCGGCCATA[A/C]AGCCTCCAGATGGCC | 51433 |
rs145096975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321685 | TGGAATTACAGGTGC[A/G]CGCCACCATGCTCAG | 51433 |
rs145133882 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328628 | TTAAAAGGAAAGTAC[C/T]TATAACCTGGCCTTA | 51433 |
rs145225603 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347288 | AGATGGATCCATAAG[G/T]AATAATAAAATTTGG | 51433 |
rs145225775 | in-del | -/TT | 0.0287284 | 0.116357 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324811 | CAGGTTGAGGTGGAG[-/TT]TTCAAGGCTGCAGTG | 51433 |
rs145354580 | snp | G/T | 0.00199481 | 0.0315187 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308013 | TCGTGAGCAGCCACA[G/T]GAACCACAAGCGCTG | 51433 |
rs145410389 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342555 | TAAAAAAAATTAAAA[A/C]CTCTTAGAAGAAAAC | 51433 |
rs145471995 | snp | G/T | 0.000428244 | 0.0146266 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335628 | ACTTTTGCTTTCGGC[G/T]CCGGTAAGAATCAGA | 51433 |
rs145508722 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318295 | CGCAAAAGCCAAGTT[C/G]AGCACTGTTTCAGAG | 51433 |
rs145667932 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324192 | ACTCATGATAAAGCT[G/T]CCTTCTCTGCAGCTG | 51433 |
rs145735955 | snp | A/C/T | 0.00434325 | 0.0464002 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330541 | AAAGAGACAAAGGCT[A/C/T]GACCATTTATGGAAA | 51433 |
rs145755944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339786 | TTTGCCTGTTAATTA[C/T]GTTAAAACAAGTCCT | 51433 |
rs145924442 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337905 | CAGTGCCTGTATGGG[A/G]CCTTATGGGAGCCAG | 51433 |
rs145944568 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341625 | TAGAACAAAAATATT[A/C]ATTGTAGAATCGAGG | 51433 |
rs146018829 | snp | C/T | 0.299158 | 0.245119 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320688 | GCTCATTGCAAGCTC[C/T]GCTTCCCGGGTTCAC | 51433 |
rs146091696 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340445 | GGTAAGGTAAGGAAG[A/G]ATCCAGCTGTACTTT | 51433 |
rs146141345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341923 | GCACATAACGGGCCT[A/G]TGCCACAACACACAT | 51433 |
rs146166745 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344910 | AGTTCCAAAGGGTTT[A/G]GGCAGAAAAGTGCTG | 51433 |
rs146249623 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355680 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 51433 |
rs146286251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317041 | TTCAGAATAGGCAAA[C/T]TCATAGAGACAGAAA | 51433 |
rs146296663 | snp | C/G | 0.000612923 | 0.0174953 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320472 | GCCCTAAAGTAGAAA[C/G]ACACAATTTGATCAG | 51433 |
rs146402769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338916 | ATGTTTATAATACAG[A/G]GTGTATTCCAAATTT | 51433 |
rs146461498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313006 | AAGAAGATCTCAAAT[C/T]AATAAGCGAATCTTC | 51433 |
rs146576669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331108 | GGTTTCTCTTCTTTC[A/T]TGGCAAGTTGCATTA | 51433 |
rs146587849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335880 | CCCTAGAGGCAGAAT[A/G]AAACAGCTTCAAGAC | 51433 |
rs146732546 | snp | A/G | 0.0150606 | 0.0854603 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307748 | GCCTCCCAAACTGCT[A/G]GGATTACAGGCGTGA | 51433 |
rs146743799 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312115 | GAATGAAATCATACA[A/C]AGAATCTCCTCTGAT | 51433 |
rs146915919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314262 | AAATTACTTGGGCAT[A/G]GTGGTGCACACCTGT | 51433 |
rs146935401 | snp | C/G | 0.000399281 | 0.0141238 | missense | ANAPC5 | GRCh38.p7 | 12:121308654 | CTTTGCAAAATAGTT[C/G]TTGGCTTCATTGAGG | 51433 |
rs147084340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315191 | AAAAATTTCATTTAA[A/G]TTACCATCAAAAAGA | 51433 |
rs147106808 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319297 | GGAGGCAATGGTGCG[A/C]TCTTGGCTCACTGCA | 51433 |
rs147155453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329080 | GGAGCCACTTTTGTC[A/G]TTATAATCAATTCTG | 51433 |
rs147178738 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333144 | GATATGGTGAAATCC[C/T]ATCTCTACTAAAAAT | 51433 |
rs147260587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346329 | TGTTTACTTTTACCA[A/G]CTGGCTCCCCCAACC | 51433 |
rs147280511 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348659 | GACAGAGCAAGACTC[C/T]GTCTCCAATAAAAAA | 51433 |
rs147306166 | snp | A/C/T | 0.000352091 | 0.0132639 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352183 | CGCCGCTCCATGAGG[A/C/T]TGACGGCGCCCTCGC | 51433 |
rs147495931 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310548 | TGAGACAAAGTCTTG[A/G]TCTGTTGCCCAGGCT | 51433 |
rs147672484 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342662 | TCAAGAGATCAAGAC[A/C]ATCCTGACCAACATG | 51433 |
rs147746301 | snp | C/T | 0.000115341 | 0.00759324 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308552 | GAAGAGCATCGCACA[C/T]CGGTTCCTCTCCTGG | 51433 |
rs147849925 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343267 | ATATAAAGTAGCTAG[A/G]AAAAGGATTACACTG | 51433 |
rs147971964 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347373 | GGTTGCTCACACTTG[C/T]AATCCCAGCACTTTG | 51433 |
rs148025794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344071 | CAGTTACCAGTATGG[A/G]TGATGGACTATATAT | 51433 |
rs148117423 | snp | C/T | 5.09498e-05 | 0.00504701 | intron-variant, missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352159 | GGCAGGAGCAGCTGG[C/T]TGAGCCTCCGCCGCT | 51433 |
rs148185195 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309395 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 51433 |
rs148267359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326814 | AAAACACACAAACCT[C/T]TGCTACCTTAAATGT | 51433 |
rs148319073 | snp | A/G | 8.375e-05 | 0.00647055 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121318420 | CTGCCACGGACAGTA[A/G]GACACTGACCGTAAA | 51433 |
rs148425102 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321513 | GTGCATGCCACCACA[C/T]ACCTGGCTATACAAA | 51433 |
rs148551902 | snp | C/T | 0.00035696 | 0.0133549 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346097 | TACGCAATGGCAACT[C/T]CACAATGGCAATGAC | 51433 |
rs148581684 | snp | A/G | 1.654e-05 | 0.00287571 | missense | ANAPC5 | GRCh38.p7 | 12:121308488 | GTCCTCTCTAGAGAT[A/G]GTTTATCAAGGGTAC | 51433 |
rs148709783 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311852 | AAAATAAAACAAAAC[A/G]AAAACCACAATAATA | 51433 |
rs148813674 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313318 | GTGACAAGAGCTAAA[C/T]TCCATCTCAAAAAAA | 51433 |
rs148884719 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343389 | ATATGAATTTATCAT[C/T]TAATTCTGACAACCC | 51433 |
rs148940916 | snp | A/G | 0.113685 | 0.209567 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339940 | GGAGTGCAGTGGTGT[A/G]ATCTCGGCTCACTGT | 51433 |
rs149021724 | snp | A/G/T | 0.000222296 | 0.0105403 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351114 | CAGTGGCTCACTCCT[A/G/T]TAATCCCAATACTCT | 51433 |
rs149057486 | snp | A/G | 6.60273e-05 | 0.00574537 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330640 | CAGAACATAGCTATC[A/G]GATCTCTTCTGCCCC | 51433 |
rs149180697 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319352 | ATTCTCCTCCCTCAG[C/T]CTCCCAAGTAGCTGG | 51433 |
rs149213493 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329685 | CAATGGCACAATCTC[A/G]GCTCACTGCAATCTC | 51433 |
rs149330193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332228 | TTGGCCTCCCAAAGT[G/T]CTGGGATTATAGGCA | 51433 |
rs149347809 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316419 | TGACTCAGCAATTCC[A/G]TTCGTAGGCATCAAA | 51433 |
rs149351292 | snp | C/T | 1.64792e-05 | 0.00287042 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347859 | ATTAACTTGTAAAGT[C/T]TTGACAGTGTAATAT | 51433 |
rs149413106 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345358 | AAGAACACATTCAAA[C/T]TGAGTAGTCTGAGAA | 51433 |
rs149448471 | in-del | -/AAG | 0.445328 | 0.156035 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315500 | TCCTGAAAAAGAACA[-/AAG]AAGACTCCCACTTCC | 51433 |
rs149562185 | snp | A/C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354251 | GACCCGCCCATCTCC[A/C/G]CCTCCAAAAGTGCTG | 51433 |
rs149669679 | snp | A/G/T | 0.000170635 | 0.00923528 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352339 | TCGTGGACGCTGGCC[A/G/T]TGGCGGCCCGAGACT | 51433 |
rs149719053 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321164 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 51433 |
rs149801264 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339763 | CATGAGCTGCCACGC[C/G]CATCCTGTTTGCCTG | 51433 |
rs149854864 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335227 | CTGGAGTGCAATGGC[A/G]TGCTCTCGGCTCACT | 51433 |
rs149950177 | snp | C/G | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346752 | ATATAGATCAAAACA[C/G]TAAGGCAATAAATAC | 51433 |
rs150107628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313153 | CAACATGGCGAAACC[C/T]CGTCTCTATTAAAAT | 51433 |
rs150238916 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323315 | TTTTTATACTCTTAT[A/T]TTGTCGGGATGTTTA | 51433 |
rs150259373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310112 | GTCTTTACAAAAAGA[C/T]CCAGCATTAATATCC | 51433 |
rs150336422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341402 | TTTAACCCAGGAGGC[A/G]GAGGTAGCAGGGACC | 51433 |
rs150386567 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337208 | GGCAACAGAGTAAGA[C/T]TCTGTTTCCAAAAAC | 51433 |
rs150469729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348296 | AAATACTATTTTTCA[C/G]AAACACAATCTCATT | 51433 |
rs150507920 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352222 | CTCATCTCGTTCAGC[A/G]GCACCAGCACCGCGA | 51433 |
rs150628928 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316140 | GGTAAAGGATCGGAA[C/T]AGACGTTTCTCCAAA | 51433 |
rs150722189 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333972 | TTCAGCTTGTCTACA[A/T]CCCTTTTAAAGCCTC | 51433 |
rs150840587 | snp | A/G | 0.0755793 | 0.179102 | splice-donor-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354101 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCGAG | 51433 |
rs150858594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342284 | AATGGTTTTTGGCAA[C/T]AGTGCCAAGACCATT | 51433 |
rs150954477 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355930 | TCCTCATCAATCGTT[A/T]TTGGGTTTTTTGTTT | 51433 |
rs151007874 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349993 | CGGGGTTACAGGTGT[A/G]ATCCCACCCGGCCTT | 51433 |
rs151113884 | snp | A/C | 0.105214 | 0.203807 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322848 | GCCAACATGGTGAAA[A/C]CCCATCTCGACTAAA | 51433 |
rs151167417 | snp | C/G | 7.23288e-05 | 0.00601325 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318235 | ACAGACTCACCAGCT[C/G]TTGAGCACAAATATG | 51433 |
rs151169485 | snp | A/G | 8.25008e-05 | 0.00642212 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335574 | GGCAAGATTCAGAGC[A/G]GCGTATCTCAAGCTC | 51433 |
rs151231719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346518 | ATCAAAGAAACACCA[C/T]GTATGCCCTCACTTT | 51433 |
rs151249117 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336471 | TCACCTGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 51433 |
rs151305333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329923 | CCCAGCCAGATAAGC[C/T]TTTTCAATGCCCCTC | 51433 |
rs180823096 | snp | A/C | 0.000351285 | 0.0132484 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319835 | TAGTAAGAAAAAAAA[A/C]CACAATTAAGTACAA | 51433 |
rs180844832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338807 | TTCTGATTTTGTTAA[A/G]AATATGTGTATACAT | 51433 |
rs180865243 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348570 | CTTGGGAGGCTGAGG[C/T]GGGAGAATGGCTTGA | 51433 |
rs181044194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315087 | AACCATAAAAAAAAA[A/G]TCCCCAAAACCTGTT | 51433 |
rs181089113 | snp | A/C/G | 5.65076e-05 | 0.00531518 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352388 | GCGCTGCCGCCAGTT[A/C/G]TCACCACAAGGCACA | 51433 |
rs181090624 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334475 | AAAAAGCCACAGGGC[A/C]GGTGGGGGGGTGAAG | 51433 |
rs181298858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310114 | CTTTACAAAAAGATC[C/T]AGCATTAATATCCTT | 51433 |
rs181417368 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328738 | GGCTTTAGCATTAGA[G/T]GGACCTGGACTTAAA | 51433 |
rs181508855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347980 | CCCCTCTGCTTTAAT[A/G]ATCACTCCAAACATG | 51433 |
rs181552451 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314117 | AATGAAAGAAAAAAT[A/C/T]GGGGCTGGGCGCAGT | 51433 |
rs181572768 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344594 | CTCAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 51433 |
rs181688271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322940 | AAAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 51433 |
rs181694460 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351281 | GGGAGGCTGAGGTGG[A/G]AGGATCACCTGAGCC | 51433 |
rs181838447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339608 | CCCAAGTAGCTGGGA[C/T]GACAGGCACATGCCA | 51433 |
rs181874908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333508 | GAGAGGTTATTAAAT[A/G]TGGGAAGACCAAAAG | 51433 |
rs181923885 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309165 | AAAAAAAAAAAAAAA[A/T]AAAGGCCGGGCGCAG | 51433 |
rs181929864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347098 | TCAAATAATGTATTT[C/T]ACAGGCAATTCAGAG | 51433 |
rs182024296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322573 | CAAATTTATATCATC[A/G]TAGTATTTTATCGGG | 51433 |
rs182041276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344126 | GAACACATTCTATGA[A/G]TCAGGCACTCTACTA | 51433 |
rs182176815 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329684 | GCAATGGCACAATCT[C/T]GGCTCACTGCAATCT | 51433 |
rs182180827 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311040 | CAAACTTTTTTTTTT[A/T]AAAGTATCCACTGTA | 51433 |
rs182213979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328032 | TGCGTTTGCGATCGC[A/G]GGTAGATCAGATGTG | 51433 |
rs182221986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334961 | AGGGGGCAGACTATT[C/T]AGGCAGAAGGTTTTC | 51433 |
rs182505444 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353186 | CTGAGTCAGTTTCCT[A/G]CCTAATAAACTACAA | 51433 |
rs182525995 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316088 | AATAATTTTTACAAG[G/T]GAACATCAAAAAGAT | 51433 |
rs182542330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317329 | CACGATCCTGGCTCA[C/T]TGCAACCTCCGCCTC | 51433 |
rs182562904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335848 | AATAAGATGGTCATA[A/G]TTTAGCTTAATCTTC | 51433 |
rs182613260 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355354 | TTGAGGTCAGGAGCT[C/T]GAGACCAGCCTGGGC | 51433 |
rs182622322 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321015 | AGCACTTTGGGAGGC[C/G]AAGACGGGTGGATCA | 51433 |
rs182780278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340138 | CCTGCCCAACATGGC[A/C]AAATCCCGTCTCTAC | 51433 |
rs182826414 | snp | C/G | 0.000888777 | 0.0210618 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330680 | AGCCAGCTCTGGCAA[C/G]AGAAATCATCAAAAT | 51433 |
rs182826635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344837 | AAAGAGGTCAGGGAA[A/G]TTCATTGGGCCAGGT | 51433 |
rs182838269 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312906 | ACACAGACTCTCATT[A/T]ATGAAATTTGTGGGA | 51433 |
rs182891017 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340514 | AATCTGTTTGAAATT[A/C]ATCTGCAGAGGTAAT | 51433 |
rs183066670 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316608 | CGTGGTGGCGGGCGC[C/T]TGTAGTCCCACCTAC | 51433 |
rs183067066 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354580 | AGAAGACATTGATAT[A/C]TTGTAATACAAGCTT | 51433 |
rs183120222 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321687 | GAATTACAGGTGCGC[A/G]CCACCATGCTCAGCT | 51433 |
rs183167864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324022 | TCCTCTGGGTTGCAA[A/G]AGGAAGCTCAGAAAG | 51433 |
rs183182366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341145 | TCCAGCCTCAGTGAC[A/G]GAGTGAGACTCCGTC | 51433 |
rs183370126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320777 | CCGGCTAATTTTTTT[C/G]TATTTTTAGTAGAGA | 51433 |
rs183386258 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324808 | TAGGCAGGTTGAGGT[A/G]GAGTTCAAGGCTGCA | 51433 |
rs183439072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325226 | CCAACACTCTGGGAG[A/G]CCAAGGCAGGTGGAT | 51433 |
rs183442997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345712 | GCCCTTATCAGTTAA[C/T]TTCCCAGATCTGGAA | 51433 |
rs183463508 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349768 | GCTGGAGTGCAGTGA[A/T]GTGATCTCAGCTCAC | 51433 |
rs183687286 | snp | C/G/T | 0.000197682 | 0.00994023 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345921 | TATCAGCATCCTCCA[C/G/T]TGTCTTTTTCTCACC | 51433 |
rs183712343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349667 | GAATTCCAAACAGCA[A/G]AAAACAACATGAGCA | 51433 |
rs183720546 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307822 | GATGAATTCCTGGAC[A/G]TAATTTATCATCATC | 51433 |
rs183782885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313199 | GGCGTGGTAGCATGC[A/G]CCTGTAATCCCAGCT | 51433 |
rs183787682 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350383 | CACAGCTTCACACTT[G/T]CTGTAAGAAATCCTC | 51433 |
rs183792379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331066 | TAGTATACATCTTTT[C/G]TTAATGCCAGTGCTA | 51433 |
rs183913114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330202 | CACTCAGCCTGAAGC[C/T]CCTAAGTAGGCAGAA | 51433 |
rs184031745 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308287 | AAAAAGTTGGTGTCC[C/T]TTGCTACCAAAAGGG | 51433 |
rs184094759 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325749 | GTGGACACCTATAGT[C/T]CCAGCTATTCGGGAG | 51433 |
rs184135618 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333916 | TATGATATGGCTTTG[A/T]ATGTCTCAACACCCT | 51433 |
rs184141433 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314958 | TTTATTCAACATGTA[C/T]TGGAAGTTTTACTCA | 51433 |
rs184189601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351876 | GAAGATACAGGATCT[C/G]AGACTCTAACTCTCA | 51433 |
rs184408951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337755 | TGAGATCCTATAAGC[A/C]CCTCCATGCTCCCAT | 51433 |
rs184429406 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322232 | GGTGTGGTCTAGGCT[C/T]ACTGCAACCTCCACC | 51433 |
rs184574551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342978 | GTAATTTCTTTTAGA[C/T]AAAGAATTATAATCA | 51433 |
rs184686579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318974 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 51433 |
rs184692462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346289 | TTTCTTCATGGCTGT[C/T]ACACTATCTGAAATG | 51433 |
rs184803934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338546 | GTGAGCCGAAATCAC[A/G]CCACTGCACTCCAGC | 51433 |
rs184884471 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348615 | GGTTGCAGTGAGCCA[A/C]GATCACGCCATTGCA | 51433 |
rs184888600 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329756 | AAGTAGCTGGGATCA[C/G]AGGCATGTCCCACCA | 51433 |
rs185066884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327445 | GCGAGGAGACACGTA[C/G]TGGTTAGGGCACAGC | 51433 |
rs185073213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308899 | CATGCCTGTAATCCT[A/G]GCACTTTGGGAGGCC | 51433 |
rs185074235 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322034 | CCACGCCCAGCTAAT[A/T]TTTGTATTTTTAGGA | 51433 |
rs185075143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346769 | AAGGCAATAAATACA[A/T]ACTGCAACACCTCCA | 51433 |
rs185132727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352400 | GTTGTCACCACAAGG[C/T]ACAACACTACCGGGT | 51433 |
rs185139063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334654 | TAAAAACAGAGGCAC[A/G]CTGAGGCAACAGTAT | 51433 |
rs185142091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324536 | TTACTTTTTAGGGTC[C/T]TACTCCCAGAAAAAA | 51433 |
rs185381141 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329176 | GGGTTGTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 51433 |
rs185391765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310518 | CAGTGAGCCACAATC[A/G]TGCCACTGCACTCCA | 51433 |
rs185457608 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348494 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAACA | 51433 |
rs185465156 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350836 | GGTGGAGGTTACCGT[A/C]TAATGGGAGAGAAGG | 51433 |
rs185483819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313547 | AAGACTCAAATAACC[A/G]AAGTCAGGGATGACA | 51433 |
rs185741023 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336572 | TACTCCCAGCTACTC[A/G]AGAGGCTGAGGCAGG | 51433 |
rs185785400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339066 | TTTCTTTTTTTTTTT[C/T]TTTTTTGAGACAGAG | 51433 |
rs185801038 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311549 | ACAATTCAACAATAA[G/T]AGGCCAGGCACAGTA | 51433 |
rs185848670 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355831 | CCACTGCACTCTAGC[C/T]TGGACGACAGAGTGA | 51433 |
rs185863234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317490 | AACTCCTGACCTTGT[A/G]ATCTGCCCACCTCAG | 51433 |
rs186147010 | snp | G/T | 0.029116 | 0.117091 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320621 | TTTCTTTTTTTTTTT[G/T]GGGACAGAGTCTCGC | 51433 |
rs186163408 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339761 | GGCATGAGCTGCCAC[A/G]CCCATCCTGTTTGCC | 51433 |
rs186176181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315355 | AGCATTAAGATGGCA[A/G]TGTTCTCCAAACTGA | 51433 |
rs186215910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345134 | AGGAAGGACTGACTG[A/G]ATCTGCTGAGGGACT | 51433 |
rs186363271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322712 | GCATACTGGTCCAAT[G/T]ATTTCCTTAGCATAA | 51433 |
rs186377495 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344145 | GGCACTCTACTAAAC[A/G]CTGGGGAAATGTGAT | 51433 |
rs186475906 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321261 | TCTCAAAAAAAAAAA[A/T]TTTTTTTTAATTACA | 51433 |
rs186538080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340193 | TGTGGTGGCAGGCAC[C/T]TCTAATCCCAGCTAC | 51433 |
rs186583704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344646 | CCTCGTGGTCAGGGA[G/T]GCCCGTCTGAGGAAA | 51433 |
rs186681440 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350551 | CCGGGCGTGGTGGCG[A/G]GAGCCTATAGTCCCA | 51433 |
rs186824552 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322993 | TCACACCACTGCACT[A/C]CAGCCTTGGCCCCAG | 51433 |
rs186869704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328701 | GGAGAGAGGCAGAGG[A/G]TACACGGGAAAGAGC | 51433 |
rs186900379 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355555 | GAGCAAAAACTCCAT[C/T]TCAAAAATAAATAAA | 51433 |
rs187026075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347223 | AAAATTTGTCAAACT[A/G]TCACATCAACCAATA | 51433 |
rs187045922 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309188 | GGGCGCAGTGGCTCA[C/T]ACCTATAATCCCAGC | 51433 |
rs187110877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316159 | CGTTTCTCCAAAGAA[C/T]ATATGCAAATGGCCA | 51433 |
rs187119656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330834 | GAGACCTGTCAAACA[C/T]ATCAACATCATTAAA | 51433 |
rs187125094 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313054 | AAAGAGGCCGGGCGC[A/G]GTGGTTCACGCCTGT | 51433 |
rs187125352 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349829 | TTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 51433 |
rs187180438 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353644 | ACGGGGTGTCACCGT[A/G]TTAGCCAGGATGGTC | 51433 |
rs187353514 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316686 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 51433 |
rs187366959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334974 | TTTAGGCAGAAGGTT[C/T]TCATAAACTGTTCCA | 51433 |
rs187369824 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354929 | AAAATCCTAAATAAC[A/T]ATTTTACTGTAAATT | 51433 |
rs187373101 | snp | A/G | 7.15948e-05 | 0.00598266 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335756 | CAATGTATTTTAAAC[A/G]CTGTAAATATCTCTG | 51433 |
rs187474185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341567 | ATATCAAAAAATAAG[A/C]TGAAATGGTGGCTGA | 51433 |
rs187491625 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321752 | CATGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGG | 51433 |
rs187502448 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313210 | ATGCGCCTGTAATCC[C/T]AGCTACTCGGGAGGC | 51433 |
rs187506039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340607 | AGTAGCGCAATCTTG[A/G]CTCACTGCAACCTCC | 51433 |
rs187719892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345724 | TAACTTCCCAGATCT[A/G]GAAGGGTAAAAAGGG | 51433 |
rs187721282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336077 | TAAAGATCCTAAAAC[C/T]TGAATTCATATACAA | 51433 |
rs187749307 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325188 | TAAAAACTGGCTGGG[C/T]GCGGTGGCTAACGCC | 51433 |
rs187763678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331575 | TTATTCTCTCAGAGG[C/T]GTGCCCCAACCCTAG | 51433 |
rs187956876 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320810 | GGGTTTCACTGTGTT[A/C]GCCAGGATGGTCTCG | 51433 |
rs187997345 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317395 | AGTGGCTGGGATTAC[A/G]GGCACGTGCCACCAC | 51433 |
rs188149908 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322415 | CTGCCCACCTCAGCC[A/C]CCCAAATTGCTGGGA | 51433 |
rs188159306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343696 | ACTCATAGAAAGTGC[A/G]ATAAGCATTCCCCAT | 51433 |
rs188191540 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121307999 | GGACCAACAAGTCCT[C/T]GTGAGCAGCCACAGG | 51433 |
rs188383048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326110 | GCTGGCAAAGGCGCC[A/G]TGGAACCCATCAGTC | 51433 |
rs188407170 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346390 | GTCTATCTTACACGT[C/T]CAGAGCCTGGCACAT | 51433 |
rs188419370 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308311 | AAAAGGGAAGAAAAG[A/G]GGAATAAAACAAATA | 51433 |
rs188510287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330215 | GCCCCTAAGTAGGCA[A/G]AAAGCCAGATTTGGC | 51433 |
rs188544731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325412 | AGGTTGCAGTGAGCT[A/G]AGATCACACCATTGC | 51433 |
rs188547487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351975 | CGTAAACGCTCAGTA[C/T]GTGTTAGCTACCGGT | 51433 |
rs188555375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334176 | TAGTCACAGCTAGGA[A/G]GCTGAGATGGACTGC | 51433 |
rs188589078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315051 | TCTCTATTTGCAGAT[A/G]ACATGATCTTATACA | 51433 |
rs188723500 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312263 | ATGCAATGAGGTGTA[C/T]AAAAATACCACAGAC | 51433 |
rs188749344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317598 | AATCACTGAGGAAGG[C/T]AGTAAGAAACAGATT | 51433 |
rs188798508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338060 | CCAATTTTACCTAGA[C/T]GAGTTTTTCTATAAG | 51433 |
rs188800981 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355924 | CTACAATCCTCATCA[A/G]TCGTTATTGGGTTTT | 51433 |
rs188803644 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349717 | ACCAGAATCACTGTT[C/T]CTATTTTTTTTTTTT | 51433 |
rs188832984 | snp | A/C/G | 3.3298e-05 | 0.00408021 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318449 | AAGAGGAAAACACAG[A/C/G]ATGAGAAGATCCACC | 51433 |
rs189021718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336604 | GAATCACTGAGAACC[C/T]GGGAGGCAGAGGTTG | 51433 |
rs189245489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322761 | GGTGCGGTAGCTCAC[A/G]CCTGTAATCCCAGCA | 51433 |
rs189260197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344542 | TGAGTCAAGATTGTG[C/T]CATTGCACTCCAGGC | 51433 |
rs189351568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338666 | TTATTCCAAAAATAT[A/G]GAAAACCTACAGAAG | 51433 |
rs189507304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346771 | GGCAATAAATACAAA[C/T]TGCAACACCTCCAAC | 51433 |
rs189510319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327797 | AAGTGGCTAAATGTG[A/C]AAGTACACAATAAGA | 51433 |
rs189571110 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319407 | CTGGCTAATTTTTTG[A/T]ACTTTTAGTAGAGAG | 51433 |
rs189607276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322047 | ATATTTGTATTTTTA[A/G]GAGAGACAGGGTTTC | 51433 |
rs189629448 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345231 | CTTCCTTACAACAGC[G/T]TCCTTAGAGGCTAGA | 51433 |
rs189657948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324609 | GGCTAAAGAATTGAG[A/C]CACAAGGCACTGTGA | 51433 |
rs189845410 | snp | A/G/T | 0.000165378 | 0.00909195 | missense | ANAPC5 | GRCh38.p7 | 12:121309715 | CCTTCTGCTTTCTTC[A/G/T]GCTGATCGTAGGAAG | 51433 |
rs189863699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348542 | TGGTGGCACACACCT[A/G]TAGTCCCAGCTACTT | 51433 |
rs189874449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342498 | CTTAGAAGATCTTCC[G/T]TCCACCTGCTAGTAA | 51433 |
rs189904583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329443 | AGGTGTGAGCCACCA[C/T]GCCAGGCCGATTTTA | 51433 |
rs189909896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310869 | AACCCAGGAGGTAAT[A/G]GATGCAGTGAGCAGA | 51433 |
rs189919555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347562 | CCTGAGCTCAGGAAG[C/T]CCAGGCTGCGTTGAG | 51433 |
rs190100550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333072 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 51433 |
rs190115314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328707 | AGGCAGAGGGTACAC[A/G]GGAAAGAGCCAGCAG | 51433 |
rs190328174 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317323 | CGGTGTCACGATCCT[A/G]GCTCACTGCAACCTC | 51433 |
rs190338306 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355343 | AGGCAGATCACTTGA[A/G]GTCAGGAGCTCGAGA | 51433 |
rs190339084 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313909 | TGGGGCCACTATTAC[C/T]CTAATACTAAAGCCA | 51433 |
rs190340300 | snp | C/T | 0.000576462 | 0.0169676 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335758 | ATGTATTTTAAACGC[C/T]GTAAATATCTCTGGT | 51433 |
rs190420301 | snp | A/G/T | 0.0286704 | 0.116912 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351234 | AAAAATTAGCTGGGC[A/G/T]TAGTGACCCGCGCCT | 51433 |
rs190567775 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320691 | CATTGCAAGCTCCGC[C/T]TCCCGGGTTCACGCC | 51433 |
rs190585352 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339914 | GGAGTGTCGTTCTTG[C/T]GGCCCAGGCTGGAGT | 51433 |
rs190651527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315769 | AAGAATAAGAGTGGA[A/G]CCCTATCTCATAGTA | 51433 |
rs190667168 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309089 | GGGAGGCAGAGGTTG[A/C/T]AGTGAGCTGAGATCA | 51433 |
rs190727132 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352677 | GGGCTGAAGGGACTG[A/T]GGAGCTCCCAAAGTG | 51433 |
rs190795625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316447 | AAATGAAAACAGGTA[C/T]TCAACCCCGGGCGCG | 51433 |
rs190946342 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340327 | ATCTCAAAAAAAAAA[A/C]AAAAACCAACAATGT | 51433 |
rs190967572 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334923 | GGCTAGGCACTAAGA[C/G/T]GGCAATGTTACATAG | 51433 |
rs190970310 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121348670 | ACTCCGTCTCCAATA[A/T]AAAAAAAAGAGTACC | 51433 |
rs191042943 | snp | A/C/G | 9.88768e-05 | 0.00703062 | missense, synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121320391 | GCAGATTACCTGGGC[A/C/G]TGCTGACTATTAGGC | 51433 |
rs191199094 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320868 | TCAGCCTCCCAAAGT[A/G]CTGGAATTACAGGCG | 51433 |
rs191205473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323575 | GAGCTCAAGTGATAC[A/G]CCTGCTTCAGCCTCC | 51433 |
rs191407598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326584 | CGGTTGGAGACCTGC[C/T]TCTGACATTTACAGG | 51433 |
rs191426274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346519 | TCAAAGAAACACCAC[A/G]TATGCCCTCACTTTG | 51433 |
rs191436763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344828 | AATAAAGAGAAAGAG[A/G]TCAGGGAAGTTCATT | 51433 |
rs191502632 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349743 | TTTTTTTTTGGAGAC[A/G]GATGCCCAGGCTGGA | 51433 |
rs191636855 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330883 | AGTCATTGTTCTGCT[C/T]CACCTGACAGCCACT | 51433 |
rs191640033 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313070 | GTGGTTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 51433 |
rs192001770 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321933 | TGCAGTGGCATGATC[G/T]CAGCTCACTGCAACC | 51433 |
rs192029502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329968 | AGGACTATAATTCAC[A/G]GCCTTCCCTATCACT | 51433 |
rs192060201 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354280 | TGGGATTACAGGCCT[A/G]AGCCACTGTGCCTGG | 51433 |
rs192071688 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342472 | AATGTGAGGCCAAAA[A/G]CCGTAAAACTCTTAG | 51433 |
rs192295835 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339086 | TTGAGACAGAGTCTT[G/T]CTCTGTCGCCAAGGC | 51433 |
rs192301156 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121355754 | AATCCCAGCTACTTG[C/G]GAGGCTGAGGCCGGA | 51433 |
rs192310752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311922 | AAAAATTAGACAGAA[A/G]ATCAGCAAGGAAAGA | 51433 |
rs192339715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337730 | GCTTCTGTCACCTTC[C/T]AGATGAAGGTGAGAT | 51433 |
rs192342706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317671 | GCAAGGCCTCAGGTA[C/T]GAAGATATTTTTTAA | 51433 |
rs192558707 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340700 | TGGGATTACAGACGG[C/G]CATCACCACACCCGG | 51433 |
rs192602215 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321269 | AAAAAAATTTTTTTT[A/T]AATTACACACGTAAG | 51433 |
rs192646762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336287 | ACTATTTAAGAAAAT[C/T]TTCCGAGTAAAAAAT | 51433 |
rs192734197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325702 | TGAAACCTCATCTCT[A/G]CTAAAAATACAAAAA | 51433 |
rs192820677 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322106 | CATGACCTCGTGATC[C/T]GCCTGCCTCGGTCTC | 51433 |
rs192873605 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312503 | TGAGGTCAGGAGATC[A/G]AGACCATCCTAACAC | 51433 |
rs192948610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346144 | TCCTTCAGAAGAGTA[A/T]GAAAGAGACACTTGC | 51433 |
rs192958876 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308138 | AGAGCTCTTGTCTGA[A/G]AATAGGTGCTAAATG | 51433 |
rs193117156 | snp | C/T | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332521 | CTATCTGAGATATTA[C/T]AACTATGCTTAGCGT | 51433 |
rs193212743 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325190 | AAAACTGGCTGGGCG[C/T]GGTGGCTAACGCCTA | 51433 |
rs193267308 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313301 | ATTGCACTCCAGCCT[C/T]GGTGACAAGAGCTAA | 51433 |
rs193286006 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350810 | ACAAAAACAGGACTA[A/G]GTACTGAGCTGGTGG | 51433 |
rs199640158 | snp | C/T | 1.94626e-05 | 0.00311945 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319658 | AAAACCATTTAACAA[C/T]TATTTTATTCTGGGG | 51433 |
rs199648147 | in-del | -/T | 0.0356815 | 0.128715 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321261 | TCTCAAAAAAAAAAA[-/T]TTTTTTTTAATTACA | 51433 |
rs199651766 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335661 | ATCAAAATAATGGAG[G/T]AGACTGTGTGTTGAA | 51433 |
rs199680151 | snp | A/G | 0.000345566 | 0.0131402 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327082 | GAAGCACGTGGGCCC[A/G]GCCACCTGCCTACCT | 51433 |
rs199705811 | snp | A/G | 0.000313306 | 0.0125122 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308697 | GCCTCCAGAGCTGAC[A/G]GAAAGGGGAAAATAA | 51433 |
rs199925143 | snp | A/G | 6.59435e-05 | 0.00574172 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328405 | CCAGTGCAGGAGGTC[A/G]GAGTCCTTTAGGGCA | 51433 |
rs199951770 | snp | A/C | 0.00199798 | 0.0315436 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346994 | AACTCGCCTTCAGCC[A/C]TCAGTTTGATTCTGA | 51433 |
rs200039400 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327010 | AACTGTCCAACACGT[A/G]TCCAGTGCTTTCCTC | 51433 |
rs200074790 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340538 | AGGTAATTCCGTAAA[-/T]TTTTTTTTTTTTTTT | 51433 |
rs200078162 | snp | C/T | 0.00199792 | 0.0315431 | missense | ANAPC5 | GRCh38.p7 | 12:121308559 | ATCGCACACCGGTTC[C/T]TCTCCTGGGTCTTCC | 51433 |
rs200230127 | snp | A/G | 0.00199806 | 0.0315443 | missense | ANAPC5 | GRCh38.p7 | 12:121320449 | ACTTCAGAAGCTGCA[A/G]CAAAACAGCCCTAAA | 51433 |
rs200315604 | in-del | -/TG | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339871 | GTTTTCTTCCAGTTT[-/TG]TTTTTTTTTTTTTTT | 51433 |
rs200539545 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331579 | TCTCTCAGAGGCGTG[A/C]CCCAACCCTAGCAGC | 51433 |
rs200571344 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321204 | TGGTGCACTGAGATC[A/G]TGCCATTGCACTCCA | 51433 |
rs200700631 | snp | G/T | 0.000116596 | 0.00763441 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337275 | AACACAGCAACAAAT[G/T]CTGGGAAAGACTTAC | 51433 |
rs200789659 | snp | C/G/T | 6.60037e-05 | 0.0057444 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318495 | GATGTACAAGAGACC[C/G/T]CTTACCTGATCACCA | 51433 |
rs200823029 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328342 | CAGCCTCCAGATGGC[C/T]GTTTTCTGTGCGATG | 51433 |
rs200963566 | in-del | -/C | 0.0244538 | 0.107838 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317412 | GCACGTGCCACCACG[-/C]CCGGCTAATTTTTGT | 51433 |
rs200968974 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308597 | ATGGTAGAGTCTGGC[C/T]TGGAAGTAAACGACG | 51433 |
rs201004490 | snp | A/G | 6.64739e-05 | 0.00576477 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347924 | GGATTTTAAAGAGCT[A/G]GAGACTGATAAAGAA | 51433 |
rs201038764 | snp | A/G | 1.654e-05 | 0.00287571 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330584 | AAGATGAGCCTTACC[A/G]GTAACCCAAAATGTA | 51433 |
rs201109196 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352013 | ATCTTTATTTCTTCA[C/T]GTTCCTCCAGGCAGG | 51433 |
rs201214898 | snp | A/G | 1.6501e-05 | 0.00287232 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121309795 | GTCCAGGATAGCCCC[A/G]TCAGCCAAGATGGGC | 51433 |
rs201254620 | snp | C/T | 0.000296663 | 0.0121755 | missense | ANAPC5 | GRCh38.p7 | 12:121328368 | CGATGCTGATATCGA[C/T]GAGCTCTGACAGGCT | 51433 |
rs201349222 | snp | C/T | 1.67304e-05 | 0.00289222 | splice-acceptor-variant | ANAPC5 | GRCh38.p7 | 12:121318426 | CGGACAGTAGGACAC[C/T]GACCGTAAAGAGGAA | 51433 |
rs201386198 | snp | A/G | 6.61901e-05 | 0.00575245 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318476 | CACCACCACATCTCC[A/G]TGAGATGTACAAGAG | 51433 |
rs201395836 | in-del | -/GTTGTTGTTGTT/TT | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352707 | GTTTTTTTGTTGTTG[-/GTTGTTGTTGTT/TT]GTTGTTGTTGTTGGT | 51433 |
rs201464964 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339872 | TTTTCTTCCAGTTTT[-/G]TTTTTTTTTTTTTTT | 51433 |
rs201536561 | in-del | -/AG | 0.146985 | 0.227789 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320903 | CCACCATGCCTGGCC[-/AG]AGACTCAAATTTCTA | 51433 |
rs201565505 | snp | A/C | 1.69115e-05 | 0.00290782 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345816 | TCACAGGAAAAGGAT[A/C]CCTGTCAGAAAAGCC | 51433 |
rs201582258 | in-del | -/T | 0.228547 | 0.249078 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329618 | CAAGCTTGTGCTTCC[-/T]TTTTTTTTTTTTTTG | 51433 |
rs201634790 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335590 | GCGTATCTCAAGCTC[C/T]GGCCATAGCCCTCTT | 51433 |
rs201693033 | snp | C/T | 0.000168779 | 0.00918483 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309675 | CTGGAATAGCATTGC[C/T]TAACAGTCTTCGTAC | 51433 |
rs201698453 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325511 | AATTAAAAATTAAAA[A/T]AAAAAAAGAATTGAA | 51433 |
rs201734457 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349575 | CACTCTAAAAAAATT[-/A]AAAAAAAAAATAAAT | 51433 |
rs201834054 | snp | A/G | 0.00199792 | 0.0315431 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346002 | AAGAAAGCTTACTGT[A/G]GGCCAAGATCATGTG | 51433 |
rs201855949 | snp | A/G | 1.73159e-05 | 0.00294239 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328533 | ACGACCCAAGATAGA[A/G]ATTACATGACAGAAT | 51433 |
rs201961617 | in-del | -/ACAA | 0.274661 | 0.248781 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319111 | GCATGCTGTGTATAC[-/ACAA]ACACACACACACACA | 51433 |
rs202023687 | in-del | -/A | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338582 | GACAGGGCAAGACTC[-/A]AGTCTCAAAAAAACA | 51433 |
rs202072221 | snp | C/T | 0.477853 | 0.102875 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316758 | AAAAAAAAAAAAAAA[C/T]AAAACAGGTGTTCAA | 51433 |
rs202166878 | in-del | -/AATAAGATG | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341561 | AAATATATATCAAAA[-/AATAAGATG]AAATGGTGGCTGAAT | 51433 |
rs367550046 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315374 | TCTCCAAACTGACCT[A/G]CAGATTCAAATACAA | 51433 |
rs367672185 | snp | A/G | 0.000329435 | 0.01283 | missense | ANAPC5 | GRCh38.p7 | 12:121308637 | CGCTCTTTGCAGTCA[A/G]CCTTTGCAAAATAGT | 51433 |
rs367701247 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350537 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 51433 |
rs367817165 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121337986 | CAATTATATAAAATA[C/T]GTAGAAAGTTAGCTA | 51433 |
rs367817326 | in-del | -/C | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319116 | CTGTGTATACACAAA[-/C]ACACACACACACACA | 51433 |
rs368001928 | snp | C/T | 3.92495e-05 | 0.00442981 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352098 | ATGCTCAGTAAAAGT[C/T]TGCTGCACGAGCAGG | 51433 |
rs368017839 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343721 | CCCCATTTATAAACA[A/G]TGTCACCCCCTGCCA | 51433 |
rs368024007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316401 | TTAAACACAAAATTA[C/T]CATGACTCAGCAATT | 51433 |
rs368058151 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350778 | CATTCTAGGAGGCTT[-/T]GGGGATGTACCAGTA | 51433 |
rs368102538 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | ANAPC5 | GRCh38.p7 | 12:121328386 | GCTCTGACAGGCTGT[A/G]TTTCCAGTGCAGGAG | 51433 |
rs368132972 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333626 | CTGATGTTTGAATAC[C/G]CTTAATAACATCTTT | 51433 |
rs368193512 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332550 | GTTGTTTATTCCCTA[G/T]TTCCCCTGATATAAG | 51433 |
rs368194221 | snp | A/G | 8.58082e-05 | 0.00654956 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331469 | CCCATTAATAATCAC[A/G]AACATGCATAAGCAA | 51433 |
rs368249432 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314851 | GTCCAGGCTGGTCTC[A/G]AACTCCTGGCCTTAA | 51433 |
rs368257208 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320752 | GGACCACAGGTGCCT[A/G]CCACCATGTCCGGCT | 51433 |
rs368276376 | snp | A/C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344663 | CCCGTCTGAGGAAAG[A/C/T]TGAGCTGTGATCTGA | 51433 |
rs368305060 | snp | A/G | 5.04053e-05 | 0.00501997 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309866 | TTCCAAGAATGAGCT[A/G]AAAAAGAAACATCAT | 51433 |
rs368463935 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340698 | GCTGGGATTACAGAC[A/G]GGCATCACCACACCC | 51433 |
rs368484764 | snp | C/T | 4.99521e-05 | 0.00499736 | missense | ANAPC5 | GRCh38.p7 | 12:121327116 | CCGCGTGTAGCTCTG[C/T]GAGGTGGCAGAGTGC | 51433 |
rs368577703 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350738 | CTCTATCGCATTTCA[C/T]TCATTTTACAAAAAA | 51433 |
rs368605285 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316758 | AAAAAAAAAAAAAAA[-/G]AAAACAGGTGTTCAA | 51433 |
rs368606735 | snp | C/T | 1.65817e-05 | 0.00287933 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347764 | ATTTTCATCTACCTT[C/T]ACACCTTTTCATATA | 51433 |
rs368709917 | in-del | -/GTTTTGTTT | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353438 | GTGCCTTGTGCCTTT[-/GTTTTGTTT]TGTTTTGTTTTGTTT | 51433 |
rs368729676 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327432 | CTGGATGTGCAGCGC[A/G]AGGAGACACGTAGTG | 51433 |
rs368877111 | snp | A/C | 3.35801e-05 | 0.00409743 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121342038 | CTGCTTGTTTTTGGG[A/C]CAGAGGCCCACTGCA | 51433 |
rs368900204 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347204 | TTGTTGTTTTCTTGA[C/T]CATAAAATTTGTCAA | 51433 |
rs368930697 | snp | C/T | 9.88924e-05 | 0.0070311 | missense | ANAPC5 | GRCh38.p7 | 12:121308535 | TCCTGATGCAGCTGC[C/T]GGAAGAGCATCGCAC | 51433 |
rs368946538 | in-del | -/A | 0.173965 | 0.238157 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312879 | GCAAGGCTCTGTCTC[-/A]AAAAAAAAAATACAC | 51433 |
rs369115044 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334480 | GCCACAGGGCAGGTG[G/T]GGGGGTGAAGGGATC | 51433 |
rs369123565 | snp | A/G | 5.22425e-05 | 0.00511063 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335507 | GTTCCTTCAATTTGC[A/G]CAAGGACAAAGGTCT | 51433 |
rs369148501 | snp | C/T | 0.000197723 | 0.00994094 | utr-variant-5-prime, missense | ANAPC5 | GRCh38.p7 | 12:121347842 | GTGGACAAGACTCTT[C/T]AATTAACTTGTAAAG | 51433 |
rs369174498 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121317960 | TCATTTCTTTATTCA[C/T]ATCCCCTTGTTGCTA | 51433 |
rs369267306 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328906 | GTCAAACAGTGCTGC[A/G]CACATATGTAATAGG | 51433 |
rs369320958 | snp | C/G | 0.000184191 | 0.00959488 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331438 | TGTTGACTAATGACA[C/G]ACTAAACATTAATAT | 51433 |
rs369366104 | snp | A/G | 4.94205e-05 | 0.0049707 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308621 | AACGACGTCCCTGAT[A/G]CGCTCTTTGCAGTCA | 51433 |
rs369385246 | snp | A/G | 5.0104e-05 | 0.00500494 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335541 | AACTTACTAGTGACC[A/G]AAGCGGCAGTGCAGG | 51433 |
rs369406067 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329354 | AGACGAGCTTTTACC[A/G]TAACGGTCAGGCTGG | 51433 |
rs369413518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339696 | CTGGTCTCGAACTCC[C/T]GACCTCAAATGATCC | 51433 |
rs369480295 | snp | A/C | | | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121354277 | TGCTGGGATTACAGG[A/C]CTGAGCCACTGTGCC | 51433 |
rs369565783 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345912 | TCAGTTCCATATCAG[C/T]ATCCTCCACTGTCTT | 51433 |
rs369665440 | in-del | -/CGTCCA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351619 | CCGCCACCACGTCCA[-/CGTCCA]GCTAATTTTTTGTGT | 51433 |
rs369699372 | snp | A/C | 0.000153988 | 0.00877328 | stop-gained | ANAPC5 | GRCh38.p7 | 12:121308626 | CGTCCCTGATGCGCT[A/C]TTTGCAGTCAACCTT | 51433 |
rs369743249 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323900 | AAAAATATTCCCATC[A/G]TGGCCTGCAATTCCT | 51433 |
rs369753396 | snp | C/T | 1.71272e-05 | 0.00292632 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330689 | TGGCAAGAGAAATCA[C/T]CAAAATATATCATAA | 51433 |
rs369765214 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338735 | ACGCTATTAATACTT[C/T]AGTGTATATTATCCT | 51433 |
rs369797495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318167 | TACCTTTCCAGACGT[C/T]AATATGAACAAATGA | 51433 |
rs369805668 | snp | A/C | 0.000168522 | 0.00917783 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352376 | CGGGCCCGCGGCGCG[A/C]TGCCGCCAGTTGTCA | 51433 |
rs369843287 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318635 | TCAAAATGAACACAA[A/G]TGTTTTAACTAGTCA | 51433 |
rs369898477 | snp | A/G | 0.000118148 | 0.00768507 | missense | ANAPC5 | GRCh38.p7 | 12:121318371 | AGGAGCATGGGCAGC[A/G]CGATGGTAGGGGAGG | 51433 |
rs369934710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329866 | GTGATCCACCCACCC[C/T]GGCCTCCCAAAGTGC | 51433 |
rs369937244 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331250 | TTTGCTGCTGAAGAT[-/T]CTCTGCTCCAACTGC | 51433 |
rs370126114 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121311420 | AGGAAAAAGGAGGAC[A/G]TTATATACTCATGAA | 51433 |
rs370149756 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324779 | AGGTGGTGTGCACCT[A/G]TAGTCCCAGCTACTA | 51433 |
rs370239348 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352743 | TGGTGGTGGTTGTCG[C/T]TGTTGTTGTTTGAGA | 51433 |
rs370345225 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344594 | TCAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAAGA | 51433 |
rs370418052 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313870 | AGAAAAAGGAGAAGA[A/G]AGAATACTTTCTAAC | 51433 |
rs370468197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330498 | CCATTCTAAATCTAT[C/T]GCTGGTTAATGACAG | 51433 |
rs370620501 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332425 | GTTGAGTGACCTGTA[C/T]ATGTATCTGGAGTAA | 51433 |
rs370628749 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342107 | AATAGTAAAGAATTA[C/T]ACAAAAGTAAAAATG | 51433 |
rs370641273 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326708 | AGACAGTACCCATAA[A/G]ATAGGCACAGGGACT | 51433 |
rs370670517 | in-del | -/CT | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121321196 | AGAGGTTGTGGTGCA[-/CT]GAGATCGTGCCATTG | 51433 |
rs370672887 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349720 | AGAATCACTGTTTCT[A/T]TTTTTTTTTTTTTTT | 51433 |
rs370673612 | snp | A/G | 0.00119952 | 0.0244606 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121345453 | CAGTCCCCAGGACTG[A/G]TAACAGTGGGGTACC | 51433 |
rs370754318 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319687 | GGTTAGAGTTTTCAA[A/G]GTTTCTTACCTATAA | 51433 |
rs370763275 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312209 | CATACTCTTAAGTAA[A/C]CAATGTGTCAAAGAA | 51433 |
rs370811261 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349514 | ATGGTAAGCTAGGAT[A/C]GCACCACGGCACTCC | 51433 |
rs370901184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320085 | TAGATACCAATGAAG[C/T]CCTTTGCAAATTCTA | 51433 |
rs371017962 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332305 | GGATTCCCACTTCTG[A/T]AATATTTTTTCCTTT | 51433 |
rs371062195 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352940 | TCAAATAGAATGTTT[-/A]AATGATTGTGTTTAA | 51433 |
rs371151967 | snp | C/T | 1.69447e-05 | 0.00291068 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309660 | AACTTTCAATGCTTT[C/T]TGGAATAGCATTGCC | 51433 |
rs371157572 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324393 | CTTCTAGTTGTGTAC[C/T]AAAAGGCTTCCTAAC | 51433 |
rs371233998 | snp | A/G | 4.96019e-05 | 0.00497981 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121327165 | GTTGTTCTGCTGCAC[A/G]CCCGCATTCACCGCC | 51433 |
rs371290988 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328019 | GTCACTTGTTAACTG[A/C/T]GTTTGCGATCGCGGG | 51433 |
rs371336108 | snp | A/G | 0.000414246 | 0.0143858 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318270 | ATAAAAACAGAGATC[A/G]GCTTACCTGCGCAAA | 51433 |
rs371351583 | snp | C/T | 5.28322e-05 | 0.00513939 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121327059 | ATGGTAGAGCCTCCA[C/T]TGCTCCAGAAGCACG | 51433 |
rs371418158 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322633 | TGGTTTTTGATATTT[C/T]GGTTATTTCTAATAT | 51433 |
rs371434186 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351098 | ACATGACGGCCGGGC[G/T]CAGTGGCTCACTCCT | 51433 |
rs371469277 | in-del | -/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352343 | GACGCTGGCCATGGC[-/G]GGCCCGAGACTAAGT | 51433 |
rs371470685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328636 | AAAGTACCTATAACC[C/T]GGCCTTAACCCTGAG | 51433 |
rs371525321 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121328439 | ATCAGCTTGTTTGCC[A/G]TCTTCCCAGCAAAAG | 51433 |
rs371615799 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309990 | ACCTGACATGTACTA[C/T]GTTAAAACAGGAACC | 51433 |
rs371719600 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333906 | ACATTACTTATATGA[C/T]ATGGCTTTGAATGTC | 51433 |
rs371799358 | snp | A/C/T | 3.3748e-05 | 0.00410769 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341979 | TAGAACAGAAGTTCA[A/C/T]GATAAATTACAGAAT | 51433 |
rs371839663 | snp | C/T | 0.000378085 | 0.0137441 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309897 | GGCACTGTACATACC[C/T]AAACCCACTGCCCTT | 51433 |
rs371872787 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308874 | GTCTTTAAGACTGGG[C/T]GAAGTGGCTCATGCC | 51433 |
rs372139978 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326937 | CAACTTTGCAGACTC[C/T]ACCCTTGGTCCCCTT | 51433 |
rs372152082 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | ANAPC5 | GRCh38.p7 | 12:121308028 | GGAACCACAAGCGCT[A/G]GTTCAGTCCAACAAG | 51433 |
rs372186574 | snp | A/G | 1.65488e-05 | 0.00287647 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345993 | CTTGGCTGAAAGAAA[A/G]CTTACTGTAGGCCAA | 51433 |
rs372244715 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342100 | AAACAAAAATAGTAA[A/C]GAATTACACAAAAGT | 51433 |
rs372331169 | snp | A/G | 0.00014855 | 0.00861703 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347891 | TGGGCCCTGTGTAAA[A/G]GAGAGATAGGGAGGT | 51433 |
rs372451754 | snp | C/T | 6.60709e-05 | 0.00574727 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330598 | CGGTAACCCAAAATG[C/T]ACTGCCTTCTTCACA | 51433 |
rs372485822 | snp | C/G | 5.13949e-05 | 0.00506901 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335521 | CGCAAGGACAAAGGT[C/G]TATAAACTTACTAGT | 51433 |
rs372504555 | snp | A/G | 3.55006e-05 | 0.00421296 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330703 | ATCAAAATATATCAT[A/G]ACAGTGGCAATGGCT | 51433 |
rs372720294 | in-del | -/GA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320906 | CCATGCCTGGCCAGA[-/GA]CTCAAATTTCTAAGG | 51433 |
rs372759993 | snp | G/T | 0.000394548 | 0.0140399 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352377 | GGGCCCGCGGCGCGC[G/T]GCCGCCAGTTGTCAC | 51433 |
rs372818058 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121329099 | TAATCAATTCTGTAC[A/G]TATGAGTTTCTTTCC | 51433 |
rs372968831 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341598 | ATAGAGAGTGGTTAG[A/G]TAAGTAATAAATAGA | 51433 |
rs373004230 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331505 | GCAGGAAGTCATCTG[C/T]ACACAGTCATCCAAA | 51433 |
rs373022933 | snp | C/G | 1.65633e-05 | 0.00287774 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318637 | AAAATGAACACAAGT[C/G]TTTTAACTAGTCACT | 51433 |
rs373065302 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353682 | CCTGACCTCGTGATC[C/T]TCCCGCCTCGGCCTC | 51433 |
rs373110905 | snp | A/G/T | 3.70482e-05 | 0.00430383 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352370 | AAGTCTCGGGCCCGC[A/G/T]GCGCGCTGCCGCCAG | 51433 |
rs373131860 | snp | A/G | 1.69324e-05 | 0.00290962 | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121352161 | CAGGAGCAGCTGGTT[A/G]AGCCTCCGCCGCTCC | 51433 |
rs373153436 | in-del | -/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344647 | TCGTGGTCAGGGAGG[-/G]CCCGTCTGAGGAAAG | 51433 |
rs373173396 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318041 | TCACTGAAGAGGCGA[A/G]TCCTCCTTACTGAAT | 51433 |
rs373194952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352020 | TTTCTTCACGTTCCT[C/T]CAGGCAGGGAGAGTA | 51433 |
rs373195408 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | ANAPC5 | GRCh38.p7 | 12:121308639 | CTCTTTGCAGTCAAC[A/C]TTTGCAAAATAGTTC | 51433 |
rs373299039 | snp | C/T | 3.30098e-05 | 0.00406249 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308717 | GGGGAAAATAACACA[C/T]ACATTTAACTCAACC | 51433 |
rs373415393 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352129 | AGCCAGCGGGCGCCT[C/T]TCACCTGCAGCAGGG | 51433 |
rs373562790 | snp | A/G | 8.23811e-05 | 0.00641746 | missense | ANAPC5 | GRCh38.p7 | 12:121308554 | AGAGCATCGCACACC[A/G]GTTCCTCTCCTGGGT | 51433 |
rs373604461 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121342000 | ATTACAGAATTCACA[C/T]ACCTGTTGAGAAAGA | 51433 |
rs373699821 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310401 | CCTGTCTCAAAAAAC[A/C]AATTTAAAACAATTA | 51433 |
rs373837134 | snp | G/T | 1.76512e-05 | 0.00297074 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328541 | AGATAGAGATTACAT[G/T]ACAGAATTTGTTTTG | 51433 |
rs373880794 | snp | A/G | 0.000197681 | 0.00993988 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121335642 | CTCCGGTAAGAATCA[A/G]ACGATCAAAATAATG | 51433 |
rs373904844 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320695 | GCAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 51433 |
rs373921421 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313622 | CAAGAATACCATGAA[C/G]AATTCTATGCAAGAA | 51433 |
rs374015840 | snp | C/T | 8.31981e-05 | 0.0064492 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121337291 | CTGGGAAAGACTTAC[C/T]GCTTCAGCAAAATCA | 51433 |
rs374016636 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330097 | AGAGAGTAAATAATT[C/T]CGATTTTTCAGGCCA | 51433 |
rs374112460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325745 | GGTGGTGGACACCTA[C/T]AGTCCCAGCTATTCG | 51433 |
rs374135868 | snp | G/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352710 | TTTTTTGTTGTTGGT[G/T]GTTGTTGTTGGTGGT | 51433 |
rs374144611 | snp | A/G | 3.29919e-05 | 0.00406138 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121328339 | ATACAGCCTCCAGAT[A/G]GCCGTTTTCTGTGCG | 51433 |
rs374232851 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347189 | TTCTGAAAAGTATCA[C/T]TGTTGTTTTCTTGAT | 51433 |
rs374343484 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121356144 | TAGAGATAGAGTCTC[A/G]CTGTGTTGCTCAGGC | 51433 |
rs374369112 | snp | C/G/T | 3.35931e-05 | 0.00409822 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121309686 | TTGCCTAACAGTCTT[C/G/T]GTACAGCTTCCTACC | 51433 |
rs374524956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343037 | TTTCTTCAATTTTCA[C/T]GATGAAATTCAGTTT | 51433 |
rs374535083 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324106 | CATACCACAAAACAA[C/T]GTGCACCATCCAATT | 51433 |
rs374638714 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350728 | ACTCATCCACCTCTA[C/T]CGCATTTCATTCATT | 51433 |
rs374639377 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340678 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 51433 |
rs374669386 | snp | A/G | 8.28315e-05 | 0.00643497 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308741 | CTCAACCCTTCACGT[A/G]TAGTTTTCAAAACGT | 51433 |
rs374764595 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347962 | CATAAATTCATTTAT[C/T]AACCCCTCTGCTTTA | 51433 |
rs374859800 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350574 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 51433 |
rs374939401 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121324738 | TCCATCTCTAAGAAA[C/G]AAGAATTAAAATAAT | 51433 |
rs375034304 | snp | C/T | 1.65233e-05 | 0.00287426 | synonymous-codon | ANAPC5 | GRCh38.p7 | 12:121308495 | CTAGAGATGGTTTAT[C/T]AAGGGTACCCCATGA | 51433 |
rs375081639 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333296 | TGCACTCCAGCCTGG[A/G]CAACAGAGCAAGACT | 51433 |
rs375108672 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121326102 | AGAAACCAGCTGGCA[A/G]AGGCGCCGTGGAACC | 51433 |
rs375347310 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121328025 | TGTTAACTGCGTTTG[C/T]GATCGCGGGTAGATC | 51433 |
rs375423567 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310734 | AGGTCAGGGGTTCGA[C/G]ACCAGCCTGGCCAAC | 51433 |
rs375575693 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333771 | TCTCAATCTTCTCCC[A/G]TAGCCATACCCTCAA | 51433 |
rs375639591 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318464 | GATGAGAAGATCCAC[C/T]ACCACATCTCCGTGA | 51433 |
rs375682791 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320710 | CGGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC | 51433 |
rs375724639 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320609 | AATTTCTTTTCTTTC[-/T]TTTTTTTTTTTTGGG | 51433 |
rs375952346 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343866 | GCTCTGGACAGTGTA[C/T]CTGTTTACTTGTCAG | 51433 |
rs376133573 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323891 | GTATCCCCCAAAAAT[A/G]TTCCCATCGTGGCCT | 51433 |
rs376163609 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121352116 | CTGCACGAGCAGGAG[C/G]CAGCGGGCGCCTCTC | 51433 |
rs376223210 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310933 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 51433 |
rs376304104 | snp | A/C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335029 | AAGTTACTGACTAGT[A/C/G]CAGGTTGATGAGCTG | 51433 |
rs376467619 | snp | C/T | 1.69186e-05 | 0.00290844 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341969 | ATCACAGGACTAGAA[C/T]AGAAGTTCATGATAA | 51433 |
rs376590849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332379 | TGATCTGCTACCTTT[C/T]TATTTAACCAGAGAT | 51433 |
rs376706141 | snp | A/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341372 | CTATTTGGGAGTCTG[A/T]TGCATAAGAATAGCT | 51433 |
rs376710093 | snp | A/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121330656 | GATCTCTTCTGCCCC[A/T]GCACATAAAGCCAGC | 51433 |
rs376863108 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121346990 | CTTCAACTCGCCTTC[A/G]GCCATCAGTTTGATT | 51433 |
rs376970952 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121341053 | GAAATGTTTGGGCTG[C/G]GCGTGGTGGCTCACA | 51433 |
rs376997360 | snp | C/G | 3.36774e-05 | 0.00410336 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331336 | CTCCCAAGACCAGAG[C/G]ATGGCCTCACCAAAC | 51433 |
rs377123840 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, utr-variant-5-prime | ANAPC5 | GRCh38.p7 | 12:121345871 | TTCTTCTTTTTCCAT[C/T]TTTCTTTCACCCTCA | 51433 |
rs377175953 | snp | C/T | 0.000153988 | 0.00877328 | splice-acceptor-variant | ANAPC5 | GRCh38.p7 | 12:121319819 | ACATAGCATCCATAA[C/T]TAGTAAGAAAAAAAA | 51433 |
rs377207134 | snp | C/T | 0.00208904 | 0.0322515 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352379 | GCCCGCGGCGCGCTG[C/T]CGCCAGTTGTCACCA | 51433 |
rs377231485 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350863 | AAGGCCATCACTCAC[A/G]TAACCATGAATATAA | 51433 |
rs377282055 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353856 | CCTCAGCCTCCAGTT[A/T]AAGTAGGTAATTAGA | 51433 |
rs377285552 | snp | A/G | 3.29783e-05 | 0.00406055 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121308695 | CAGCCTCCAGAGCTG[A/G]CGGAAAGGGGAAAAT | 51433 |
rs377308371 | in-del | -/TGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG/TGTTGTTGGTGGTGG/TGTTGTTGGTGGTGGTGGTGGTGG | 0.499997 | 0.00119808 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352718 | GTTGGTTGTTGTTGT[lengthTooLong]TGGTGGTGGTGGTGG | 51433 |
rs377328212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121325133 | TGCACCACTACATTC[C/T]AGCCCTGGTGATACA | 51433 |
rs377332140 | snp | G/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121330909 | CCACTGAGTGGCAGG[G/T]GTTTCAGAAAAAAAG | 51433 |
rs377348221 | in-del | -/AAAC | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314413 | GACACTCTATCTCAA[-/AAAC]AAACAAACAAAAACC | 51433 |
rs377350103 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121323217 | AAGTAGTACCTTAAC[C/T]GCTTTAAATTTAATT | 51433 |
rs377411877 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318914 | AATCCCAGCTACTCA[C/G]AAGGCTGAGGCAGGA | 51433 |
rs377504172 | snp | A/G | 1.70912e-05 | 0.00292324 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335523 | CAAGGACAAAGGTCT[A/G]TAAACTTACTAGTGA | 51433 |
rs377582765 | snp | G/T | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353712 | CCCAAAGTGCTGGGA[G/T]TACAGGCGTGAGCCA | 51433 |
rs386377974 | in-del | -/GAGA | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310256 | TTAAAAAAAAAAGAG[-/GAGA]AGAATTAAAATGGTA | 51433 |
rs397688754 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121332588 | CAAGTTTTTTTTTTT[-/T]CTTTTTCACTGCTGT | 51433 |
rs397702709 | in-del | -/TTTTGTTTTG | | | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353460 | TTTTGTTTTGTTTTG[-/TTTTGTTTTG]AGACGGAGTCTCCTC | 51433 |
rs397777891 | in-del | -/AGA | 0 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121315504 | GAAAAAGAACAAAGA[-/AGA]CTCCCACTTCCTGAT | 51433 |
rs397803981 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340740 | TGTGTGTGTTTTTTT[-/T]TAGCAGAAACAGGGT | 51433 |
rs398044834 | in-del | -/TT | 0.5 | 0 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322650 | GTTATTTCTAATATT[-/TT]CCATTTAAAAAATGC | 51433 |
rs527462958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333021 | AAATTCTGTTCATCA[A/G]AATATTATTTGTGGC | 51433 |
rs527475609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121340524 | AAATTCATCTGCAGA[A/G]GTAATTCCGTAAATT | 51433 |
rs527532263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347473 | CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA | 51433 |
rs527540995 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121322730 | TTCCTTAGCATAAAA[A/C]CTTAGAAGTAGGCTG | 51433 |
rs527635941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310605 | ACACACAAGAAAGCA[A/G]TAATGGAGGAACTGA | 51433 |
rs527911347 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331214 | CCTTTCTGAATTCCC[A/G]TGACCACCTAACTTG | 51433 |
rs527942776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121331669 | AGGGCATAAAGCAAA[C/G]GCTTTTATCTCCGCT | 51433 |
rs528058022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338435 | TCTACTAAAGATACA[A/G]AACATTAGCCGGGTG | 51433 |
rs528069945 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310595 | CATCTACTTAACACA[C/T]AAGAAAGCAGTAATG | 51433 |
rs528119404 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121338997 | TGTAACTTTATTTCC[C/T]GTTCTTTTCATTTTA | 51433 |
rs528129393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344316 | GAGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51433 |
rs528139320 | snp | A/C | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336652 | ACCACTGCACGCCAG[A/C]CTGGGCAACAAGAGC | 51433 |
rs528288873 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347451 | CCTAGGCAACAAAGC[A/G]AAATCCCATCTCTAC | 51433 |
rs528305787 | in-del | -/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121339873 | TTTCTTCCAGTTTTT[-/T]TTTTTTTTTTTTTTT | 51433 |
rs528312714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121316269 | ACCCACTAGGAAGGA[A/T]GTAATAATTAAAAAT | 51433 |
rs528328506 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121318746 | TTGAAAGAGGCTGAG[C/T]GCGGTGGCTCACACC | 51433 |
rs528553953 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121351335 | CCGCGATCACACTAC[C/T]GCACTCCAGCCTGGG | 51433 |
rs528562947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121336931 | ACTCAATATAAAAAG[C/T]AGCCTTGGCCAGGCG | 51433 |
rs528664019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121343192 | AAGAGAAAACCAACC[A/C]AAATAAGAAAAGTCT | 51433 |
rs528726253 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121350405 | GAAATCCTCGGGCCG[C/G]GCGCGGTGGCTCATG | 51433 |
rs528735169 | snp | A/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313413 | AATAAGGATTAAAGT[A/G]GAGATAAACAAAATG | 51433 |
rs528735477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121349986 | AAAGTGCCGGGGTTA[C/T]AGGTGTGATCCCACC | 51433 |
rs528855476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121314588 | TGATGAAAGACTGAA[C/T]GCTTTCCCCCTACAG | 51433 |
rs528907962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121320853 | CGTGATCTGCCCGCC[C/T]CAGCCTCCCAAAGTG | 51433 |
rs528920635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121313780 | AACAAAGAAAAGCCC[A/G]GGGCCAGACTGCTTC | 51433 |
rs529064666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121335248 | TCGGCTCACTGCAAC[C/T]TCCACCTCCCGGGTT | 51433 |
rs529124128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121334678 | ACAGTATAAACCAGT[A/G]TCACCTGACTGAGCA | 51433 |
rs529307347 | in-del | -/TTACAGGTGTAAGTCACCATGCCCAG | 0.0569829 | 0.158885 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121319506 | CCCAAAGTGCTGGGA[-/TTACAGGTGTAAGTCACCATGCCCAG]TTACAGGTGTAAGTC | 51433 |
rs529342035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121347665 | TTTTCAACAAAACAG[A/G]ATTAAGTAAAGGCTC | 51433 |
rs529394480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121312572 | ATTAGCCTGGTGTGG[C/T]GGCACATGCCTGTAG | 51433 |
rs529477659 | snp | C/T | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121310385 | GGCAACACAGCAAGA[C/T]CCTGTCTCAAAAAAC | 51433 |
rs529656605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121333673 | CCTCACTGACACCTT[C/T]CTCAGAGGGTTCAAT | 51433 |
rs529760706 | snp | C/G | | | intron-variant | ANAPC5 | GRCh38.p7 | 12:121344579 | ACAGTGAGACTTGAT[C/G]TCAAAAAAAAAAAAA | 51433 |
rs529892463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121353568 | GCTTCAGCCTACCGA[C/G]TAGCTGGGACTACAG | 51433 |
rs529900077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC5 | GRCh38.p7 | 12:121346474 | AAAAGCCAGAGGGAT[A/G]GAGCATGGGATAAAG | 51433 |
rs529957195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC5 | GRCh38.p7 | 12:121352549 | TGTACAAGAGTGCGG[A/G]GAGGGGTGCACCAAA | 51433 |