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 |