SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3208238 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, upstream-variant-2KB | ANAPC11, NPB | GRCh38.p7 | 17:81900284 | GGTGCCTGTGTTCTC[A/G]GCATATAGATGTGGT | 51529 |
rs8067831 | snp | G/T | 0.190519 | 0.242821 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889635 | TCAACAAAGGAAAAT[G/T]TACAACACACCCAAG | 51529 |
rs11431521 | in-del | -/A | 0 | 0 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897006 | TTTTTATTTTTATTT[-/A]TTTATTTATTTTCGA | 51529 |
rs11544150 | snp | C/T | | | upstream-variant-2KB, missense, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889242 | ACAGCAGACGTGCAC[C/T]TTGAGCGGAAGGCAG | 51529 |
rs11550400 | snp | C/T | | | missense, synonymous-codon | ANAPC11 | GRCh38.p7 | 17:81900024 | CAGCAGGTGCAGCAG[C/T]ACTGCCCCATGTGCC | 51529 |
rs11550402 | snp | A/C | | | missense, synonymous-codon | ANAPC11 | GRCh38.p7 | 17:81900042 | TGCCCCATGTGCCGC[A/C]AGGAATGGAAGTTCA | 51529 |
rs11550403 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81891824 | GCCGGCGCTGCCAAC[C/G]GAAGGGCGGGTAGGG | 51529 |
rs17352203 | snp | C/T | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896836 | AACNGGGCAAGACTC[C/T]ATCTCAAAAAAAAAA | 51529 |
rs34211234 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898446 | GACACAGTGTGCTCA[A/G]GCTTTGTTAACATGG | 51529 |
rs34442438 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889649 | GTACAACACACCCAA[-/G]GGGCTGTTCCAAGAA | 51529 |
rs34747694 | snp | C/T | 0.444444 | 0.157135 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898183 | CTGAGGGCAGGCATT[C/T]GACTTCTGGAGCAGC | 51529 |
rs34832929 | in-del | -/T | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897281 | GGGATTACAGGCATG[-/T]AGCCACTGCGCCCAG | 51529 |
rs34978095 | in-del | -/G | | | frameshift-variant | ANAPC11 | GRCh38.p7 | 17:81899952 | ACTGCCCGCTGGTGT[-/G]GGGGCCAGTGCTCCC | 51529 |
rs34992485 | snp | A/C | | | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890342 | TCTCACATTAACCCA[A/C]TAAGACAGGCACAAA | 51529 |
rs35637287 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889421 | AGCGTGAGTTGCTTT[-/G]GGGGGTGGTTCTCTG | 51529 |
rs61751632 | snp | G/T | 0.0453125 | 0.143538 | synonymous-codon, intron-variant | ANAPC11 | GRCh38.p7 | 17:81899345 | GCCCATCAACACAGC[G/T]TCCCCAACGCCTGGG | 51529 |
rs62077240 | snp | A/C | | | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890084 | TCTCCAAAACTGATT[A/C]CCAAAAAGTCATTTC | 51529 |
rs62077241 | snp | C/G | | | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81891140 | TCCGGGACCGGACCC[C/G]GAAAGAACGACCTCG | 51529 |
rs62077242 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895141 | CTCACTGCAACCTCC[A/G]CCTCCTGGGCTCAAG | 51529 |
rs62077243 | snp | C/T | | | utr-variant-3-prime, intron-variant, upstream-variant-2KB, downstream-variant-500B | ANAPC11, PCYT2, NPB | GRCh38.p7 | 17:81900480 | CGGCCCTGGGACCCT[C/T]CCTCAGGCTGGCTCT | 51529 |
rs71367088 | in-del | -/C | 0.5 | 0 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897434 | CACTGCACCCGCCCC[-/C]TGTCTTTGCTTCTTA | 51529 |
rs74006124 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899095 | TCCAGCTCCACAATG[C/T]CAGGCCGACCCTGCC | 51529 |
rs74006125 | snp | C/G | 0.00445807 | 0.0470017 | missense, intron-variant | ANAPC11 | GRCh38.p7 | 17:81899261 | TCTCCATGGAGAAAG[C/G]ATTTCTAGGTGTTTG | 51529 |
rs74006126 | snp | C/G | 0.0115965 | 0.0752581 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899579 | CCAGCCTCAAGCACA[C/G]GGGACACAGGGTGGG | 51529 |
rs79790414 | snp | C/T | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898855 | CGGGTGGGGAATGCA[C/T]TAGAACGAAGTGACA | 51529 |
rs111334610 | snp | C/G | | | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81891913 | GGAGGCGGAGCCTAC[C/G]CGCCCCTCCCTCCCC | 51529 |
rs111419775 | snp | A/G | 0.157972 | 0.232445 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894398 | GGCAGGCTTATACCT[A/G]TGTTGGTGCCTAAAC | 51529 |
rs111502339 | in-del | -/TTAGT | 0.5 | 0 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895956 | CAAACAAAAAAAAGA[-/TTAGT]TTAAACTTTTTATTT | 51529 |
rs111848880 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893481 | GTGATCCACCCTCCT[C/T]GGCCTCCCAAAGTGC | 51529 |
rs111897318 | snp | A/G | 0 | 0 | downstream-variant-500B, intron-variant, upstream-variant-2KB | ANAPC11, PCYT2, NPB | GRCh38.p7 | 17:81900717 | GAGGCTCCTTTGTGT[A/G]CCTCTGCTCCCCACA | 51529 |
rs111927478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899670 | CTGGGTGAGGGGAGG[C/T]GCCTGCTGCGGTTGC | 51529 |
rs112084595 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894171 | GCCTCAGCTACTCAG[C/G]AGGCCGAAGCACAAG | 51529 |
rs112154648 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81891785 | GCCGCGACTGTGGTC[A/G]TTTTTATACCTTCCC | 51529 |
rs112480169 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890922 | TTCCCGGCCTGAGAG[A/G]ATCCGGCCGAAACGG | 51529 |
rs113130670 | snp | A/G/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893228 | CTCCCGAGTAGCTGG[A/G/T]ATTACAGTTGCCCAC | 51529 |
rs113423282 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899585 | TCAAGCACAGGGGAC[A/C]CAGGGTGGGCTAGGC | 51529 |
rs113727280 | snp | G/T | 0.00914312 | 0.0669923 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81891770 | TGTTGAGGGAGTCGG[G/T]CCGCGACTGTGGTCG | 51529 |
rs114233604 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81888832 | GGTATCGGGGTGCTC[A/G]TGGGTGGAGAGGTGT | 51529 |
rs116480717 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899853 | TACCTGCACCCCTGC[C/T]TGGCTTGTCACATGC | 51529 |
rs137864015 | snp | C/T | 0.00205462 | 0.0319858 | stop-gained, synonymous-codon, missense | ANAPC11 | GRCh38.p7 | 17:81899936 | CAAGGTGCCCGGCGA[C/T]GACTGCCCGCTGGTG | 51529 |
rs137935308 | snp | C/G | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890252 | ACAAGGTCTTTATAA[C/G]ACAGTACTCAAGGCA | 51529 |
rs137953736 | snp | A/C | 0.0174273 | 0.0917852 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893525 | ATGAGCCACCACCTG[A/C]GGCTAATTTTTTTGT | 51529 |
rs138108291 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889702 | GCAAGGGAAGCAGTC[A/C]GATATCAGACCAGCT | 51529 |
rs138275378 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895443 | GATCCTGTCACAGAC[G/T]CCATAGGATGAAACT | 51529 |
rs138312995 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant, upstream-variant-2KB | ANAPC11, PCYT2, NPB | GRCh38.p7 | 17:81900640 | GTAGGGATCAGTGTC[C/T]TGACACTGGGAAGTG | 51529 |
rs138325924 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897055 | ACCAGGGCTGGAGTG[C/T]AGTGGCACGATCTTG | 51529 |
rs138513877 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890013 | TGCTCACTGGCCCTA[C/T]TCTGTCCTCCCAAGG | 51529 |
rs138529209 | snp | A/C/G | 0.0858192 | 0.188533 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893344 | TGATCTGCCTGCCTC[A/C/G]GCCTCCCAAAGTGCT | 51529 |
rs139036307 | snp | A/G | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896857 | TTGCCCTGTTGCTCA[A/G]ACTGGAGTGCAATGG | 51529 |
rs139217829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897009 | TATTTTTATTTATTT[A/C]TTTATTTTCGAGACA | 51529 |
rs139259052 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897831 | AAATGGAGTCTCACT[A/G]TGTTTCCCAGGCTGG | 51529 |
rs139322064 | snp | C/G | 3.3716e-05 | 0.00410571 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894458 | GTCGTCCTGTTCCCT[C/G]CGCCGCAGGCTCTGC | 51529 |
rs139387162 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895507 | AGAGTCTGGGCGGGC[A/G]GATCACAAGGTCAAG | 51529 |
rs139402425 | snp | A/C/G | 1.65102e-05 | 0.00287312 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890758 | ACCTGTCTCCACGCC[A/C/G]GCACCACCGCCGAAG | 51529 |
rs139424088 | snp | C/G | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890367 | CACAAAATTTAAAAA[C/G]CAACTGGGCTGGGTC | 51529 |
rs139430768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896678 | GGGCCAGGTGCATGC[C/T]CATATTGATTGACAG | 51529 |
rs139617866 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898499 | AGGAGTTGAGAGTCT[A/T]ATTTTTGGACCTGCT | 51529 |
rs139766589 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896509 | GGTTTTTCATGAGAC[C/T]GAAATGAGCGTAAAG | 51529 |
rs140259479 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893453 | CAGGTTGGTCTCGAA[C/T]TCCTGACCTCAAGTG | 51529 |
rs140674821 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890564 | CACTGGGTCTGTCCT[A/G]CAGCCCTTCAGAGCT | 51529 |
rs140895234 | snp | A/T | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893281 | GTATTTTTAGTAGAG[A/T]CAGGGTTTCAGTATG | 51529 |
rs141215340 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896925 | TTCAAAGGATTCTCC[A/G]GCCTCAGCCTCCCAA | 51529 |
rs141252779 | snp | A/G | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898780 | TCAGGAGACCAGCAG[A/G]TCCTGGAATGAGTCA | 51529 |
rs141281593 | snp | A/G | 0.00589927 | 0.0539892 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889276 | TAAGCTGCGACCAGA[A/G]CGATCATAGTGCACA | 51529 |
rs141544877 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890306 | CCTGTGCTTCACAAG[A/C]TACATAAAGAAGATT | 51529 |
rs141649108 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890176 | AGCTTCAACCAAAGA[C/T]GGATTTGAGAGTCAT | 51529 |
rs141853377 | snp | A/G | 0.00013282 | 0.00814814 | synonymous-codon, intron-variant | ANAPC11 | GRCh38.p7 | 17:81899354 | CACAGCTTCCCCAAC[A/G]CCTGGGCAGCACACC | 51529 |
rs141897076 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896447 | GAAAAAAAGTGGAAA[C/T]GTTTGATTATGTTTA | 51529 |
rs142010421 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897763 | TGCTGGGATTACAGA[C/T]GTGAGCCACCATGCC | 51529 |
rs142012194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894045 | GCACTTTGGGAGGCC[A/G]CAGTGGCAGATCGCT | 51529 |
rs142037924 | snp | A/T | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897000 | TTGTATTTTTATTTT[A/T]ATTTTTTATTTATTT | 51529 |
rs142049212 | snp | C/T | 0.0005644 | 0.0167893 | missense, intron-variant | ANAPC11 | GRCh38.p7 | 17:81899353 | ACACAGCTTCCCCAA[C/T]GCCTGGGCAGCACAC | 51529 |
rs142206233 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B, intron-variant, upstream-variant-2KB | ANAPC11, PCYT2, NPB | GRCh38.p7 | 17:81900953 | TAGAGAGACAGGACT[C/T]TATATGAAGAGTATA | 51529 |
rs142460219 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81888910 | GCCCCGCACTCAGAG[A/G]TGTACTATGGCGGTT | 51529 |
rs142635225 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81892957 | CAAACTCCTGGGCTC[C/G]AGCTATCCTCCCACG | 51529 |
rs142854740 | snp | C/T | 3.36956e-05 | 0.00410447 | missense, intron-variant | ANAPC11 | GRCh38.p7 | 17:81899263 | TCCATGGAGAAAGCA[C/T]TTCTAGGTGTTTGGG | 51529 |
rs143027185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896757 | ATCCTACTGTCTCAG[C/G]CTCCCAAGTAGCATA | 51529 |
rs143042197 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81889811 | CCTACTCAAGCCTGC[A/G]GCAAAGTCTGAAGTC | 51529 |
rs143094452 | snp | C/T | 1.69602e-05 | 0.00291201 | missense, synonymous-codon | ANAPC11 | GRCh38.p7 | 17:81899966 | GTGGGGCCAGTGCTC[C/T]CACTGCTTCCACATG | 51529 |
rs143294470 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895936 | CAAGACTCCATCTCA[A/G]AAAACAAACAAAAAA | 51529 |
rs143332165 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897043 | TCTCACTCTGTCACC[A/T]GGGCTGGAGTGCAGT | 51529 |
rs143371559 | snp | A/G | 0.0701645 | 0.173664 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894781 | GGAGTGCAATGGCGC[A/G]ATCTCGGCTTGCCGC | 51529 |
rs143412983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896620 | GGAATGGGGAGGACC[A/G]AGAAGCTACTCACTA | 51529 |
rs143639770 | snp | A/G | 6.60001e-05 | 0.00574419 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890773 | GGCACCACCGCCGAA[A/G]CCACTGTCGAAAAGA | 51529 |
rs143758680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81899071 | CAGGACAGGAGGGTG[A/G]CCACGAGCTCCAGCT | 51529 |
rs144025777 | snp | A/G | 0.0448719 | 0.142907 | downstream-variant-500B, intron-variant, upstream-variant-2KB | ANAPC11, PCYT2, NPB | GRCh38.p7 | 17:81900780 | CAGCCCCGGCATCTC[A/G]GGCTGCTTCTGGACA | 51529 |
rs144130608 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896694 | CATATTGATTGACAG[A/G]GTCTCACTGTGTTGC | 51529 |
rs144149412 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81898241 | CATGTGTCCACACCT[A/C/T]GTCTGGCTGCATCCG | 51529 |
rs144224512 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897625 | GGGACCACAGGCATG[C/G]TCCACAATGCCTGGC | 51529 |
rs144660827 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894332 | GGTTCGGACTCCTGG[C/G/T]CCGGTATGATCTTCC | 51529 |
rs144796634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894000 | AACGGGGCTCATAGC[A/G]GGGCATAGGGGTTCA | 51529 |
rs144847387 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893299 | GGGTTTCAGTATGTT[A/G]GCCAGGCTGGTCTTG | 51529 |
rs144896741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81896734 | ACGTGAACTCCTGGG[C/T]TCCAGCCATCCTACT | 51529 |
rs145009430 | snp | A/C/G | 0.00447073 | 0.0470678 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81894463 | CCTGTTCCCTCCGCC[A/C/G]CAGGCTCTGCTGCCA | 51529 |
rs145230119 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | ANAPC11, ALYREF | GRCh38.p7 | 17:81893524 | CATGAGCCACCACCT[G/T]CGGCTAATTTTTTTG | 51529 |
rs145274135 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81895117 | TGGAGTGCAATGGCG[C/T]GATCTCGGCTCACTG | 51529 |
rs145741918 | snp | A/T | | | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897001 | TGTATTTTTATTTTT[A/T]TTTTTTATTTATTTT | 51529 |
rs146199391 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890198 | GAGAGTCATGTCACT[A/G]ACGGGACACGGCGGT | 51529 |
rs146246997 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ANAPC11 | GRCh38.p7 | 17:81897783 | GCCACCATGCCTGAA[C/T]AAAACTACATAAATT | 51529 |
rs146289501 | snp | C/T | 1.65048e-05 | 0.00287265 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | ANAPC11, ALYREF | GRCh38.p7 | 17:81890818 | GTCGGGAAGTTGTTT[C/T]GGCTGAAAAAAAAAC | 51529 |