SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs551481200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397620 | GGAGAATGGGGGGCT[A/G]GGCGTGGTGGCTCAT | 51434 |
rs551495869 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405466 | AGGCCTGACATTCCT[A/G]TCTTCTTACGTTAAC | 51434 |
rs551521545 | snp | A/G | 1.66167e-05 | 0.00288237 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386493 | TATTTATTAAACATT[A/G]AACCTTTAAATCTAT | 51434 |
rs551534548 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404914 | AACCTCTGTCACCCG[A/C/G]GTTCAAGGAATTCTC | 51434 |
rs551707197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399060 | GAGTCTTACTCTGTC[A/G]CCCAGGCTAGAATGC | 51434 |
rs551719890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390325 | GTGATCCAACCACCT[C/T]GGCCTCCCAAAGTGC | 51434 |
rs551831480 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377189 | GATACCAACCAATTA[C/T]AGGTGGTTGGAACCA | 51434 |
rs551833447 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385558 | ATCATGGGTGCAGGC[A/G]GCTTGGAGAAGAGGA | 51434 |
rs551848139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389919 | ACTGGGAGACAGAGC[A/G]AGACTCCGTCTCAAA | 51434 |
rs552037747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383295 | TACAAAAAATTAGCC[A/G]GGCATAGTGGCACGC | 51434 |
rs552062241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377299 | GGCACACACCTGTCT[A/C]GTCATCTGTAACTAG | 51434 |
rs552120915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400849 | GTCAGGAGTTCCAGA[C/G]AAGCCTGGCCAACAT | 51434 |
rs552125500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383777 | GCTACTCAGGAGGCT[G/T]AGGCAGGAGAATCGC | 51434 |
rs552169267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384597 | AGGCTGAGGCAGAAA[A/G]TTGCTTAAACCAGGA | 51434 |
rs552182293 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388529 | AGAATGGCATCAAGG[A/G]CTAATGGGCACTGCC | 51434 |
rs552332877 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372865 | ATCAAGTGATGTTGC[A/G]CAGGCTTTGGGTCTT | 51434 |
rs552448138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388159 | CTCATGCCCCAGCCT[A/T]CCGAGAAGCTGGGAC | 51434 |
rs552580994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374965 | ATTCATTTATTTGCC[C/T]CCTAAGCAATCTTTC | 51434 |
rs552601201 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394647 | GCACTCCAGCCTGGG[C/T]AACAAGAGTGAAATT | 51434 |
rs552611779 | in-del | -/CA | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373149 | AGAAACTCCCAGCCC[-/CA]GAGCTCAGGGTGTGA | 51434 |
rs552829080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395302 | AAACATAGAGTTATC[A/G]TATGACCCAGCAATT | 51434 |
rs552936704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392448 | GCACTAACTAAAATA[C/T]ACCAGGCCCCTACTG | 51434 |
rs552958124 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389931 | GCGAGACTCCGTCTC[-/A]AAAAAACAACAAAAA | 51434 |
rs553031670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388846 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 51434 |
rs553243934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374448 | CCCAAAAAATGTGCT[A/G]AAGCCTGGCCTCTCC | 51434 |
rs553248526 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381954 | GCTGTGACAGCTGGA[-/G]AAAAAAAAAAAAAAA | 51434 |
rs553354636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401097 | CTAATGAAAATCCAA[C/T]GGGCAGCAGCAGCTG | 51434 |
rs553416234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400431 | CTATTCCACAAGAAA[C/T]TTTAAAGTATAAATC | 51434 |
rs553494765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388172 | CTTCCGAGAAGCTGG[A/G]ACTACAGGCACGCGC | 51434 |
rs553542639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394269 | GCCAAAGTGGGAGGA[C/G]AGTTTGAGCCCAGGA | 51434 |
rs553671926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387994 | GCTAAAAGGCAACTG[C/T]TTCCCTATTCTGAGC | 51434 |
rs553835723 | snp | A/C | 1.6681e-05 | 0.00288794 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386505 | ATTGAACCTTTAAAT[A/C]TATTATAAATCCTCT | 51434 |
rs553899983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398822 | TGGTGGCACATGCCT[C/G]TAATCCCAGCTATTC | 51434 |
rs553934852 | snp | A/C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374570 | GAGTTTTTCTCCACA[A/C/T]ATTTCTTAAACTTTT | 51434 |
rs553960135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401678 | GCGGGATCACCAGAG[A/G]TCAGGAGTTGAAGAC | 51434 |
rs554146799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392752 | CACTGCACACAGCTT[A/G]TATGCACCTAAACTC | 51434 |
rs554186615 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389005 | GAGAATGGTGTGAAA[A/C]CGGGAGGCGGAGCTT | 51434 |
rs554298732 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387428 | GAGAGAGAGAGAGAG[A/G]GAGACCGACCTTGTC | 51434 |
rs554334206 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396288 | TGTGGAGTAGATGCA[A/G]AATTTCCAGTTGAAG | 51434 |
rs554388133 | snp | C/T | 0 | 0 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372451 | AGGCTGCATCCTGGA[C/T]AGCATGCCTAGGCCA | 51434 |
rs554412844 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374106 | ACGGAAGTGCTCAGA[A/G]CAGGGCAGGCCACTG | 51434 |
rs554421907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385152 | GGCGCCTATAATCCC[A/C]GCTACTCGGGAGGCT | 51434 |
rs554489039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391938 | CTCCACTAAAATGCA[A/G]AAAAGTAGCTGGGCG | 51434 |
rs554600290 | in-del | -/CT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397887 | GCGACAAGAGTGAAA[-/CT]CTGTCTTTTAAAAAA | 51434 |
rs554614601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401261 | TGGAGACTCTCCAGT[C/T]AGAGAAGACCAGGTC | 51434 |
rs554671269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380706 | ACGCCTGTAATCCTA[C/G]CACTTTGGGAGGCCG | 51434 |
rs554715525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392832 | TGGAGTTTCACTCTT[C/G]TTGCCCAGGCTGGAG | 51434 |
rs554734747 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393817 | GGTTGCAGTGAGCTG[A/G]GATTGCACCATTGCA | 51434 |
rs554751373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399500 | CATACATTAGTGTTT[G/T]CGGGAGGAAGGGACA | 51434 |
rs554834369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402080 | CTTGGTTGGCTGAGG[C/G]AGGAGGATCGCTTGA | 51434 |
rs554840150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386588 | AATATAAAATTCTTC[A/G]TAATAAAAAACTTTA | 51434 |
rs554854713 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385995 | TCCCTAAAAGGATAT[C/T]ATGGTTTTAGGGATG | 51434 |
rs554886774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394353 | AAAAATTGGCCAGGT[G/T]CGGTGGCTCCCGCCT | 51434 |
rs555235817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384707 | AAAACAAAAAAAACA[A/C]AAAACCAAAGGAGCA | 51434 |
rs555376467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378336 | TGACCTCAGGTGATC[C/T]GCCCAGCTCAGCCTC | 51434 |
rs555377537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397787 | GTAATCCCACCTACT[C/T]GGGAGGTTGAGACAG | 51434 |
rs555438634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384151 | ATGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 51434 |
rs555500466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391601 | GAATGAAGGATATGT[A/G]CTGCTGACAAATGCA | 51434 |
rs555512860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390813 | TATGACTGATGGACT[A/G]TCTTTCTCAACAAAT | 51434 |
rs555571074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377808 | TCTTCCCCAGAGAAC[C/T]TGATGGATGTAGAAA | 51434 |
rs555582576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383372 | GAACCAGGGAGACAG[A/G]GGTTGCAGTGAGCCG | 51434 |
rs555623690 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380571 | CAGGAGAATGGTTTG[A/C]ACCCGGAAGGTGGAG | 51434 |
rs555696355 | snp | A/G | 4.95421e-05 | 0.00497681 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382944 | TCGTGCCAGTAGGTA[A/G]CCATATACATCCATT | 51434 |
rs555774074 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405040 | GCAACAAGGCTGTTT[C/G]TTTCACCTGGGTGCA | 51434 |
rs555995257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402121 | CGGAGGCTGCAGTGA[A/G]CCAAGACTGCGCCAC | 51434 |
rs556179306 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405264 | AGTAAGCAGGGGGTA[C/T]ATGACATGCACCGGT | 51434 |
rs556307611 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405165 | TCCTGTCTCAAGAGC[C/T]GAGCTCCCCGAGTGA | 51434 |
rs556409581 | snp | A/C | | | intron-variant, missense, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401504 | ATATCCAGGCTAAAA[A/C]CTGAAGGAGGAGGCA | 51434 |
rs556426178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379093 | TCTCGAACTCCTGAC[A/G]TCAGGTGTTCCACCC | 51434 |
rs556480365 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404349 | CACAACAATCCATAA[A/G]GTTGAAGTTGTCATT | 51434 |
rs556552139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377061 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 51434 |
rs556561886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398712 | GTTGTAATCCCAGCA[C/T]TTTGTGAGGCCAAGG | 51434 |
rs556668877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378213 | GATTCTCCTCCCTCA[A/G]CCTCCCGAGTAGCTG | 51434 |
rs556860500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397859 | GAGATTGCGCCACTA[C/T]ACTCCAGCCTGGGCG | 51434 |
rs557174062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381488 | ACTACAGGTGTGAGC[C/G]ACCATGCCCAGCTAA | 51434 |
rs557234138 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398816 | CTGGCGTGGTGGCAC[A/G]TGCCTGTAATCCCAG | 51434 |
rs557302941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374646 | AACACAAATGAAAAA[C/G]TGGCAAACAAACATT | 51434 |
rs557421248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396194 | GGCACTGGGGCCTGG[A/G]GACCCTGTTCTAAAT | 51434 |
rs557489861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388730 | ATTTACTTTTTACTG[C/G]AAAATCTACCCACAA | 51434 |
rs557633468 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390700 | AAAATGCAAAGAAAA[A/C]TACTTAAAAGGAAAA | 51434 |
rs557636655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377173 | ATTAGTGAGCCGAAT[A/G]GATACCAACCAATTA | 51434 |
rs557813174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390067 | CAATATTCCAATTTA[A/G]AATTAGATTTTTTTT | 51434 |
rs557874684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396941 | GGGTGCGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 51434 |
rs557922732 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386039 | CAGTCAGGCACACCA[C/T]AAATTTATAAGTCAT | 51434 |
rs558136526 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404158 | TTCCTGCCAAGTCAG[A/G]CTTCGGCCCTGGGGG | 51434 |
rs558285245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402162 | CATGGGCGACAGAGC[A/G]AGGCTGTCTCAAAAA | 51434 |
rs558404475 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395811 | CAAAGTGCTGGGATT[-/A]ACAGGCGTGAGCCAC | 51434 |
rs558411261 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376006 | ATAACTCCTGTGACA[A/C]AGCTCACTGCCTCCT | 51434 |
rs558458129 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393395 | CATTCTTTATTCCTT[C/T]ATTTTATTAATAAAC | 51434 |
rs558465996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403027 | TATTAGAGGCGTGAG[A/C]CACCGCGCCCGGCCC | 51434 |
rs558553556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388333 | TAAGCCACCATGCCC[A/G]GCCAAAAACCATAAT | 51434 |
rs558619667 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394942 | TTTCATCAGCTGGAT[A/G/T]TTCAGGGTCCCCCAC | 51434 |
rs558693235 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386860 | AATCCCTAGTCCTAA[C/G]CAGGCAAGCTAGGTT | 51434 |
rs558762295 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393549 | CCTGGGCAAATGGTG[C/G]AGACCATCTCTATTT | 51434 |
rs558867651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399554 | CACGGTTTCTTTTTG[A/T]TGGGATAATGAAAAC | 51434 |
rs558885045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401524 | AGGAGGAGGCAACGC[G/T]GAGATGAGGACCGTC | 51434 |
rs559010349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395038 | TTAATGCATGAGAAA[A/G]CATGGAGAGAGGGAG | 51434 |
rs559072106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402478 | GGGACTACAGGCGCC[C/T]GCCACCACGCCTGGC | 51434 |
rs559272942 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386721 | TCAGAACACAACATA[C/T]GCTACATGGTGTTAA | 51434 |
rs559364438 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382496 | TATATATATATATAT[A/T]TATAGAGACAGGGTC | 51434 |
rs559459812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379881 | TCCTTTGAACTCCCA[C/G]GGTCAATTCACATGA | 51434 |
rs559488163 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372684 | GGTGTGTACCACCAT[A/G]CCCGGTTAATTTTTG | 51434 |
rs559734609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393624 | TGTAACCCCAGCACT[C/T]TGTGAGGCCGAGGTG | 51434 |
rs559838131 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386994 | CAGCACTTTGGGAGG[A/C]CCACGTGGGAGAATC | 51434 |
rs560126467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396793 | GTGCTGGGATTACAG[G/T]CGTGAGCCATCATGC | 51434 |
rs560139517 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403903 | ACTGAGGATTTACAA[C/T]GAGACAAAAGGCACC | 51434 |
rs560153451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378571 | CCAAACAGACTGCAA[C/G]TGGCAGCCCTTGCCT | 51434 |
rs560328401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397940 | GGGATAGCAAGAGGA[C/T]TGGCCTTGATAAAAG | 51434 |
rs560446662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392192 | AAGATTATTCTTGGA[G/T]TAAGAGAAGACTTTC | 51434 |
rs560472016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399707 | AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGGTG | 51434 |
rs560743775 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378049 | AGCTGCATTCGGTCA[A/C]CTGTAGGGCTAGGTT | 51434 |
rs560750774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390335 | CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 51434 |
rs560946011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399852 | TGTAATCACAGCACT[C/T]TGGGAGGCCAAGGAG | 51434 |
rs560967258 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373867 | GTTATATAAAAAGTA[C/T]TCTTGGCCCAGAAGC | 51434 |
rs561031522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391965 | GGCGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 51434 |
rs561213848 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393721 | AAAATTACAAAATTA[C/G]TTGGGCATGGTGGCG | 51434 |
rs561395549 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378466 | AGCAACTTAGGGAGA[A/C]AGACTCTTTTATTTG | 51434 |
rs561416211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384495 | ATTCAAGACCAGCCT[A/G]GCCAAGATAGTGAAA | 51434 |
rs561480564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398884 | TGGGAGGCAGAGGTT[A/G]CGGTGAGCCAAGATA | 51434 |
rs561626744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377245 | GTTTGGTTGGGCTAA[A/T]TATAAACCAATCCAA | 51434 |
rs561638942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383678 | ACGAGGTCAGGAGTT[C/T]GAGACTAGGCTAACA | 51434 |
rs561828771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376676 | CCCAAATTCAATGAA[C/T]CAAATTATGAGTTTA | 51434 |
rs562201283 | in-del | -/CTAACT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378847 | TTAACCAGAAATTAC[-/CTAACT]CTAACTATTTTTTTT | 51434 |
rs562224300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395894 | CAGCGGTCCCCAACC[G/T]TTTTGGCACCAGGGG | 51434 |
rs562299304 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397007 | AGGAGATCGAGACCA[G/T]CCTGGCTAACGCGGT | 51434 |
rs562329843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403288 | CGTCCTCAGAGCCTC[C/T]GCCTTCTATGTCTCC | 51434 |
rs562414935 | snp | C/T | 3.30437e-05 | 0.00406457 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396375 | TTACTCACAGCATTC[C/T]GATATTCCTTATCAT | 51434 |
rs562439034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384238 | AAAATAAAATAGAAA[G/T]AAAAAAAAATTAGCC | 51434 |
rs562452826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377854 | GGCACCTTCAGTTTA[C/G]GGAAGGAAACAAGCA | 51434 |
rs562656751 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405369 | GGGGTCAGTTAAGGC[A/G]GGAACCGGCCCTTTT | 51434 |
rs562946390 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404438 | TTGACTTGGAATCAG[A/T]TCGACTGGTTAATTA | 51434 |
rs563028882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388895 | ACCATCCCGGCTAAC[A/G]CAGTGAAACCCCGTC | 51434 |
rs563054751 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389259 | AAATGGTAGAGAACG[C/T]TAGTTAACTTGATTC | 51434 |
rs563113931 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382509 | ATTTATAGAGACAGG[G/T]TCTTGCTACATTGCC | 51434 |
rs563158841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383757 | GGCGTGTGCCTGTAA[G/T]CCCAGCTACTCAGGA | 51434 |
rs563195757 | in-del | -/GA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395043 | GCATGAGAAAACATG[-/GA]GAGAGGGAGCAGGGT | 51434 |
rs563504962 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380558 | TGGGAGGCTGAGGCA[C/G]GAGAATGGTTTGAAC | 51434 |
rs563610509 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375290 | CACATGGCATGGCCA[A/G]TCTGCATGTCTGAGA | 51434 |
rs563644485 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372728 | GCGGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 51434 |
rs563819395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383174 | TTGGGCACAGTGGCT[C/G]ACACCTGTAATTCCA | 51434 |
rs563819432 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375353 | GTCACTGAGATGCTA[A/G]GCACACAAGTGGTGC | 51434 |
rs563858738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401618 | CAAAGAGGCCAGAAG[C/G]GATGGTTCACGCCTG | 51434 |
rs563876590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382632 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 51434 |
rs563901250 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376550 | CTCCAGTCTGGGCAA[A/C]AGAGCGAGACTCCAT | 51434 |
rs564068808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389518 | AATGCTACAAAAATC[A/G]GCTACACTATTTAAA | 51434 |
rs564123808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395781 | CTGACCTCGTGATCC[A/G]CCCGCCTAGGCCTCC | 51434 |
rs564138176 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399669 | GGTGGCTTATGCCTA[C/T]AATCCTAGCTACTTA | 51434 |
rs564333602 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381651 | GCTTCCCCAGATTAT[C/T]CTAACAGAGTTTGGG | 51434 |
rs564436839 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373832 | CTGTCTATTCCTTGA[A/G]CTTTTGGATTTAGAA | 51434 |
rs564441009 | snp | C/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381581 | ACCTCATGATCTGCC[C/T]GTCTCGGCCTCCCAA | 51434 |
rs564574003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374762 | TGTCCCATGTTCTTA[C/T]GATGTAATTAAACAT | 51434 |
rs564652550 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395394 | AACATGATTTACTGC[A/C]GTCTTAGACTCCTAG | 51434 |
rs564666418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400774 | AATGAGGCTGGGCTC[A/G]GTGGCTCACGCCTGC | 51434 |
rs564727991 | in-del | -/ACAAAAAAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384685 | TCTCACAAAAAAAAA[-/ACAAAAAAAAA]CAAAAAAAACAAAAA | 51434 |
rs564735258 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390217 | GGGATTACAGGCACC[C/T]GCCACCACGCCCAGC | 51434 |
rs564797519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403227 | CCTAGCGATGTGACA[C/G]TCGCGCTGCCCCGCG | 51434 |
rs565016469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386163 | TGGTATTACCTAAGC[A/G]TTAGAGACATGTGTC | 51434 |
rs565018297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378899 | AGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGGGCA | 51434 |
rs565044430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394397 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 51434 |
rs565089675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392021 | CGCTTGAACCCGGGA[A/G]GTGGAGGTTGCAGTG | 51434 |
rs565103072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379642 | CCCTCAACAAATCCA[A/G]AGGCATAGCTCTCTG | 51434 |
rs565153636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398954 | CTCCATCTCCAAAAA[C/T]AAAAACAAAAACAAG | 51434 |
rs565296816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393906 | AGCCGGACATGGTGG[C/T]TCACGCCTGTAATCC | 51434 |
rs565359889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393257 | ATTACCAAATGTGTA[A/C]ACCTATGGAAGGCAA | 51434 |
rs565502969 | snp | A/G | 0.00016728 | 0.00914396 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386514 | TTAAATCTATTATAA[A/G]TCCTCTTAGTTGCTG | 51434 |
rs565566333 | in-del | -/CAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391189 | AGAGAGACTCCATCT[-/CAAA]CAAACAAACAAAAAA | 51434 |
rs565686279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380276 | GAATCACTTAAACCC[A/G]GCAAGTGGAGGTTGC | 51434 |
rs565709206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378928 | CAGTGGTGACATCTC[A/G]GCTCACTGCAACCCA | 51434 |
rs565817115 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387233 | AGAGAGAGAGAGAGA[C/G]AGAGACAGAGAGACA | 51434 |
rs565988217 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373965 | ATACATGGAAGGTTG[A/G]TCAGGCTCTGTTTTA | 51434 |
rs566053218 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382382 | ATACAGACCTAGATA[G/T]GTAAATAATGCATCC | 51434 |
rs566117329 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385140 | GGTGTGGTGGCGGGC[A/G]CCTATAATCCCAGCT | 51434 |
rs566339757 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380220 | GCTGGGTGTGGTGGT[A/G]TATGCCTGTAATCCC | 51434 |
rs566407190 | snp | A/G | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372774 | TCAAGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 51434 |
rs566414794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378223 | CCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAAG | 51434 |
rs566452580 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404988 | ACCACTGTCATGTGC[A/G]TCCGTGTGAAGAGAC | 51434 |
rs566509936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391477 | TCCTTGTCCTTTACA[C/T]AGACTGAGAAGCCAG | 51434 |
rs566515669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396661 | GATTACAGGCACATG[A/G]CACCACACCCAGCTA | 51434 |
rs566609203 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405495 | ACAAGAAGAATAAAA[C/T]GAAATAGTCGTAAAG | 51434 |
rs566684093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390728 | AAACTCCAGGATTGA[C/T]GTCAATACTTGTAAA | 51434 |
rs566878767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389926 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAACAAC | 51434 |
rs566967667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383308 | CCGGGCATAGTGGCA[C/T]GCGCCTGTAATCCCA | 51434 |
rs566999197 | snp | A/G | 3.29837e-05 | 0.00406088 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382892 | AGATATTGAAAAGGC[A/G]GCATCCAAGGTTCTC | 51434 |
rs567281404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390461 | AAAAGAAAAAAGGTC[A/G]ACCCCCAATCTCTTC | 51434 |
rs567345132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389968 | ACAAAAACAAAAAAA[A/G]AGCCAGAAAATCTAA | 51434 |
rs567369110 | in-del | -/TACCT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392136 | CTTACAAAAGGAAGA[-/TACCT]TACCTTGAGCATTGC | 51434 |
rs567387343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399210 | ATTTTTGGTAGAGAC[A/G]GGGTTTCGCCATGTT | 51434 |
rs567534455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380004 | ATCATATGGATGTGG[A/G]GTTATCCCACGAGTA | 51434 |
rs567607529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383395 | GTGAGCCGAGATCAC[A/G]CCACTGCACTGCCTG | 51434 |
rs567699543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383888 | CTCAAAAAAAAAAAA[A/G]AAAAAAAAAAGAAAA | 51434 |
rs567789752 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373077 | CCACCCCTCACCTCC[A/G]ATTAATTGTATACTC | 51434 |
rs567908839 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396086 | ATAAGAATCTAATGC[A/C/T]GCAGCTGATCTGACA | 51434 |
rs567913613 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401667 | AGGCCGAGGCGGCGG[A/G]ATCACCAGAGGTCAG | 51434 |
rs567933120 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375689 | AAGTTCTTAATGACT[A/G]CAGTAGATAGAAACA | 51434 |
rs568252603 | snp | A/C | 3.58083e-05 | 0.00423118 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403629 | TCTATCACATTCATC[A/C]TGCTCTGCAAAGCCG | 51434 |
rs568277676 | in-del | -/AGAAAAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400102 | TCTCCCCAGAAAAAC[-/AGAAAAAAA]ACAACAAAAAGAGTA | 51434 |
rs568495565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402871 | CTCCCGAGTAGCTGG[A/G]ACCGCAGGCACGCAC | 51434 |
rs568495896 | in-del | -/AAGCA | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373589 | GGCAAGTTACTAGCT[-/AAGCA]AAGAGGAAAACTGTT | 51434 |
rs568601005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388697 | ACCATGAAAAAGTCC[C/T]AATTTTCATTACCAG | 51434 |
rs568817218 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400937 | AATCTGTAATCCCTG[C/T]TACTCAGGAGGCTGA | 51434 |
rs568819695 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389014 | GTGAAACCGGGAGGC[A/G]GAGCTTGCAGTGAAC | 51434 |
rs568829429 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395818 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 51434 |
rs569013647 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397670 | TGGGACACCAAGGCA[A/G]GCGGATCACCTGAGG | 51434 |
rs569035903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396893 | AGAAACCTCACCACT[C/T]TGAATCCTTTTTAAA | 51434 |
rs569061916 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401189 | ACACTAATACATCTA[C/G]AGAGTAAAAGTTTCC | 51434 |
rs569094486 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404791 | TGTGTGAGACCTTCT[A/G]TTTGATTTTGGTGGG | 51434 |
rs569096874 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385330 | CTCACCCACATTCTA[C/T]AAAAAGGGACCTATG | 51434 |
rs569150609 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403405 | ACGCCCTCGCAGACC[C/T]CGGAGCCTCCGCTGG | 51434 |
rs569327816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387317 | AGAGAGAGACAGAGA[A/G]ACAGAGAGAGAGAGA | 51434 |
rs569330178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394615 | TGGGCAACTTTGCAG[C/T]GAGCCCCCATGCTAT | 51434 |
rs569349376 | in-del | -/T/TT | 0.49306 | 0.0584955 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396683 | CCCAGCTAATTTTTG[-/T/TT]TTTTTTTTTTTAGTA | 51434 |
rs569404902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388746 | AAAATCTACCCACAA[C/T]CCTGTGCAAATAAAG | 51434 |
rs569429040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382757 | TACCTCTTAAACCTG[C/T]GCTTTCAATTTATAT | 51434 |
rs569455963 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391624 | CAAATGCAGACTCAT[A/G]CAGGTGCTCTAAGAA | 51434 |
rs569489810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389099 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAGA | 51434 |
rs569505167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380713 | TAATCCTAGCACTTT[A/G]GGAGGCCGAGGCGGG | 51434 |
rs569516301 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389739 | GATTGAGACCATCCC[A/G]GCTAACACAGTGAAA | 51434 |
rs569574197 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375898 | ATATTTTAAGAAAAA[A/C]TTTTTAGAAGTCATG | 51434 |
rs569777900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381328 | TTCCCCGGATGATGT[G/T]TTTTTGTTGTTGTTG | 51434 |
rs570043139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394037 | AAAAATTAGCTGGGC[G/T]TGGTGGCGGGTGCCT | 51434 |
rs570065421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382071 | CTTATTCCAAACCAC[A/G]CTTATAGTTTTAACC | 51434 |
rs570224007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400911 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCGAATCT | 51434 |
rs570311886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403078 | GGCCAGAAAGTGGAC[C/T]CTCCTGATACACTTA | 51434 |
rs570739347 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397754 | TACAAAATTAGACGG[C/G]TGTGGTGGCGCATGC | 51434 |
rs570747254 | in-del | -/GGGAA | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373706 | AGGACAATGACTTCT[-/GGGAA]CAGGAAGCTCCCTAG | 51434 |
rs570781876 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380105 | TCTGTAATCCCAGCA[C/T]TTTAGGAGGCTGAAT | 51434 |
rs570844551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401597 | GCTTGGTGCATTCAA[A/G]TAACACAAAGAGGCC | 51434 |
rs571013660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394658 | TGGGCAACAAGAGTG[A/T]AATTCCACCTCAAAA | 51434 |
rs571146538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392699 | TTTATAAATAAAAAA[G/T]TAGTAAAGCTCACAA | 51434 |
rs571156602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399308 | TACAGGCGTGAGCCA[C/T]TGCGCCCAGCCGAGT | 51434 |
rs571263215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384546 | CAAAAACTAGCCAGG[C/T]GTGGTGGCACACACC | 51434 |
rs571392245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385843 | TCTGTTGGAGGTCCC[C/T]GTGAAGATTACCCTT | 51434 |
rs571428789 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387223 | AGCCTGGGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs571494652 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | ANAPC7 | GRCh38.p7 | 12:110372905 | GACTCATAGAAACTT[C/T]TTGCCCATTTTAAAT | 51434 |
rs571505993 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405689 | AAAGGAGCATTTGTC[A/G/T]TATAGAATGATTGGT | 51434 |
rs571610943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380576 | GAATGGTTTGAACCC[A/G]GAAGGTGGAGGTTGC | 51434 |
rs572090386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378603 | TTTCCACACCCACAG[C/T]GAGACGCCCTATGAG | 51434 |
rs572153560 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372434 | AGGAAGCCCATGAAG[C/T]GAGGCTGCATCCTGG | 51434 |
rs572177548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397993 | GCTTGCACCTGTAAT[A/C]CGAGCACTTTGGGAG | 51434 |
rs572300628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391949 | TGCAAAAAAGTAGCT[A/G]GGCGTGGTGGCACAC | 51434 |
rs572315286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398843 | CCAGCTATTCGGGAG[A/G]CTGAGGCAGGAGAAT | 51434 |
rs572362534 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381526 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCACGTT | 51434 |
rs572391983 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380575 | AGAATGGTTTGAACC[C/T]GGAAGGTGGAGGTTG | 51434 |
rs572441058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392805 | TTGTTTGTTTTTTTG[G/T]TTTTTTTGAGATGGA | 51434 |
rs572547468 | in-del | -/GCA | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401099 | ATGAAAATCCAATGG[-/GCA]GCAGCAGCAGCTGCA | 51434 |
rs572551774 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392744 | CAAGTTCACACTGCA[C/T]ACAGCTTGTATGCAC | 51434 |
rs572573472 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398908 | CAAGATAGTGTGCCA[C/T]TGCACTCCAGCCTGG | 51434 |
rs572651393 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402180 | GCTGTCTCAAAAAAA[C/T]AAAAATAAATAAACA | 51434 |
rs572662876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377179 | GAGCCGAATAGATAC[A/C]AACCAATTATAGGTG | 51434 |
rs572796068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389575 | TAGCGTAATTTAAAT[A/T]TGTAACTTTGTAAAG | 51434 |
rs572810260 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390101 | GAGACGGAGTTTCAC[G/T]CTTGTCACCCAGGCT | 51434 |
rs572874792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396945 | GCGGTGGCTTACGCC[C/T]GTAATCCCAGCACTT | 51434 |
rs572886730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390091 | TTTTTTTTTTGAGAC[A/G]GAGTTTCACGCTTGT | 51434 |
rs572887118 | snp | C/G | 1.64838e-05 | 0.00287083 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396324 | ACTTTTGAAGTTTTA[C/G]TTAGCGCTTTCTTCT | 51434 |
rs572891194 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404255 | CTGGATCCAGGAATT[A/G]GCTGATACCCATATA | 51434 |
rs572953563 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384117 | TGAGGCAGGAGAATT[C/G]CTTGAACTCAGAGGG | 51434 |
rs573234590 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382493 | ATATATATATATATA[G/T]ATTTATAGAGACAGG | 51434 |
rs573297930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381582 | CCTCATGATCTGCCC[A/G]TCTCGGCCTCCCAAA | 51434 |
rs573421593 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375143 | ATATAAATGCGGACC[A/G]ATCTGTAACATCTCC | 51434 |
rs573432232 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385812 | TGAGAACTCACTGCC[A/C]GTGTCCTAACTGCCA | 51434 |
rs573533738 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389886 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 51434 |
rs573550338 | snp | A/T | 0.000396825 | 0.0140803 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403687 | AAAGCCGGTAGAGGA[A/T]CCTTAGGGAAGACTC | 51434 |
rs573572489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383680 | GAGGTCAGGAGTTCG[A/C]GACTAGGCTAACAGG | 51434 |
rs573739870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378374 | ATTAGGATTACAGGC[A/G]TAAGCCACCGTGCCT | 51434 |
rs573901104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384784 | CTTGTCCTTCTATCC[G/T]GTGGTGTGATACACA | 51434 |
rs573912319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376384 | TCCATCCTGGCTAAC[A/G]CAGTGAAACCCCGTC | 51434 |
rs573972345 | snp | A/C | 1.66994e-05 | 0.00288953 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382985 | AAGGACATAGTGAGA[A/C]GAGGTGTTTTAAGAA | 51434 |
rs574001183 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375207 | CTCTGAAGCTCTCAC[C/G]CATACCCAGGGCTCC | 51434 |
rs574126788 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110376973 | TATAAAAAAAAATAA[A/T]AAAAAATAAAAAAAT | 51434 |
rs574146899 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404306 | ACTTAACGTTTTAGG[A/G]AAGTTTTACACAAGT | 51434 |
rs574162282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395039 | TAATGCATGAGAAAA[C/T]ATGGAGAGAGGGAGC | 51434 |
rs574188729 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376709 | ATAAATCAGGACTGA[-/A]AAAAAAAAAAAAGGG | 51434 |
rs574231243 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405054 | TGTTTCACCTGGGTG[A/C]AGGCAGGATGGTAGC | 51434 |
rs574288025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388849 | ACTTTGGGAGGCCGA[G/T]GTGGGTGGATCACGA | 51434 |
rs574354949 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402538 | ACGGGGTTACACTGT[A/G]TTAGCCAGGATGATC | 51434 |
rs574426564 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389326 | ATAAGAAAGTGAGAA[A/T]CTCTTGACATAGCTA | 51434 |
rs574604920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388091 | CCCTGGGCTGGAATG[C/T]AGTGGCACAATCTCA | 51434 |
rs574654103 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373288 | CCAGGGAAATTAACC[C/T]ACCCAATATGCAAAC | 51434 |
rs574710886 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382497 | ATATATATATATATT[G/T]ATAGAGACAGGGTCT | 51434 |
rs574889127 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394016 | CTCTACTAAAAATAC[-/A]AAAAAAAAAATTAGC | 51434 |
rs574910681 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392232 | CAGAACAGGATTTAG[C/T]ATACAGCATCCAGGC | 51434 |
rs574944063 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383068 | TGAGGCCCCAGCTCC[-/T]GCAGGGGCTAAGCCC | 51434 |
rs575083466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383092 | TAAGCCCTTTCCACC[A/G]TCACAGGCTCCTCCA | 51434 |
rs575085383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389999 | AAGTTCCTAAGAATG[C/T]AGAAGTTATAGGCAA | 51434 |
rs575187322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383411 | CCACTGCACTGCCTG[C/G]GTGACAGACTGAGAC | 51434 |
rs575525907 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376461 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 51434 |
rs575553648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394898 | GAAAAAACAAAGAAT[A/G]AGCATGTGTAGTATT | 51434 |
rs575700708 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375117 | AACCCATGTTGGCAC[C/T]GTTTCTACCGATATA | 51434 |
rs575808541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374734 | AAAAAATAGGAATTT[A/C]TCTGAGTATAGGTGT | 51434 |
rs575840005 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381507 | ATGCCCAGCTAATTT[G/T]TGTATTTTTAGTAGA | 51434 |
rs575928403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382221 | AGCAGAGAGGCATTC[A/G]GAGAATTTGTAAAGC | 51434 |
rs575944623 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372619 | CCACCTCCTGGGTTC[A/G]AGTGATTCTCCTGCC | 51434 |
rs576004792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380350 | AGTGAGACTCTATCT[C/T]AAATAAAAATAAAAA | 51434 |
rs576097591 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373146 | GGAAGAAACTCCCAG[C/G]CCCAGAGCTCAGGGT | 51434 |
rs576163808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401310 | ATTTATTGGATGTGT[A/G]AACTTGGACAAGGGT | 51434 |
rs576224424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402106 | CTTGAACCCAGGAAG[C/T]GGAGGCTGCAGTGAG | 51434 |
rs576231895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392841 | ACTCTTGTTGCCCAG[A/G]CTGGAGTGCAATGGC | 51434 |
rs576253173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394354 | AAAATTGGCCAGGTG[C/T]GGTGGCTCCCGCCTG | 51434 |
rs576448479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399521 | GGAAGGGACAATTGG[A/C]GAGTGATTACTAATA | 51434 |
rs576502160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401400 | TTATTGCGCACAGCC[A/G]CTGCGCTTTCAATTG | 51434 |
rs576522664 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391104 | CTGAGACAGGAGAAT[C/G]GCTTGAACCCAGGAG | 51434 |
rs576625808 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378255 | ATGCACCACCACACC[A/C]GGCTAGTTTTGTATT | 51434 |
rs576763928 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392762 | AGCTTGTATGCACCT[A/G]AACTCAAACTAGACA | 51434 |
rs576773852 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377091 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 51434 |
rs577098481 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395667 | CCTCAGCCTCCCAAG[A/T]AGCTGGGACTACAGG | 51434 |
rs577103305 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388367 | GTATTTCTTGATTGA[A/G]TATGTGACAACAGGA | 51434 |
rs577118118 | in-del | -/ACTGATG | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382274 | TCTTCTGGCCCCATC[-/ACTGATG]GCTCAGTACTAAGCA | 51434 |
rs577144876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380737 | AGGCGGGCGGATCAC[A/G]AGGTCAGAAGATTGA | 51434 |
rs577147903 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389006 | AGAATGGTGTGAAAC[A/C/T]GGGAGGCGGAGCTTG | 51434 |
rs577168280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392995 | AGACGGGGTTTCTCC[A/G]TGTTGGTCAAGCTGG | 51434 |
rs577231122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393589 | AAAAAAAAAATTGGC[C/T]GGGCATGGTGGCTCC | 51434 |
rs577285756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400340 | AAAGGAAATGTTGGG[A/G]TGAGGTTCAAGACTC | 51434 |
rs577322620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399654 | ATTGTGGCCATGTGC[A/G]GTGGCTTATGCCTAT | 51434 |
rs577690209 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404460 | GGTTAATTATGTTGG[A/G]TCGCAAACTCAAATG | 51434 |
rs577693205 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386083 | GACCCCCTCAAAAGA[A/G]AAAAAGCCAAATAAT | 51434 |
rs577715463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384310 | GCTAAGGCAGGAGGA[C/T]TGCTTGAGCCCAGGA | 51434 |
rs577784368 | in-del | -/TGTT | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405035 | TGTGAGCAACAAGGC[-/TGTT]TGTTTCACCTGGGTG | 51434 |
rs577846664 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402658 | TATTAAGCAGGAGAG[A/G]GACATGCACTCAAGG | 51434 |
rs577852734 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405175 | AGAGCCGAGCTCCCC[A/G]AGTGAGCAATTCCTG | 51434 |
rs577970131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377132 | ACAGAGCAAGATGCC[A/G]TCTCAAAAAAAAAAA | 51434 |
rs578092894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397869 | CACTACACTCCAGCC[G/T]GGGCGACAAGAGTGA | 51434 |
rs578169269 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398802 | AATACAAAATTAGCC[A/T]GGCGTGGTGGCACAT | 51434 |
rs745382632 | snp | C/T | 1.66302e-05 | 0.00288355 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374165 | CATGCCGAACCACTG[C/T]TCCTGGTCAGCCCAC | 51434 |
rs745392860 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395740 | AGACGGCGTTTCACC[A/G]TGTTAGCCAGGATGG | 51434 |
rs745401482 | in-del | -/AA | 0.00847878 | 0.0645562 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396226 | CTTGGAGTCTTTCTC[-/AA]AAAAAAAAAAAAAAA | 51434 |
rs745498551 | snp | C/G | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375229 | CAGGGCTCCTGCCCT[C/G]TGGACTCCCACCTTC | 51434 |
rs745656677 | snp | A/G | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381776 | AATCTAAGCGACAAG[A/G]TGCGAGCCGTATGGC | 51434 |
rs745758366 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387676 | TTTTGCTACTTCAGA[C/T]ACATCAGACTTCCAG | 51434 |
rs745764739 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401280 | GAAGACCAGGTCCAG[A/G]CATCGTACTCCTCCA | 51434 |
rs745836429 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400209 | ATGCTTAGATACAAA[A/C]GTATTATTACATCCA | 51434 |
rs745876646 | in-del | -/AC | 7.299e-05 | 0.00604067 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381973 | AAAAAAAAAAAAAAA[-/AC]ACAAAAACCCCAGAA | 51434 |
rs745915542 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381397 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 51434 |
rs746033616 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377356 | CAGGTTTTATAAAAA[C/T]TAATGATGAACAGGA | 51434 |
rs746105094 | snp | A/G | 8.4386e-05 | 0.00649507 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388659 | GATAGCAAAATAAGC[A/G]TATATTGCAAAGAAA | 51434 |
rs746138821 | in-del | -/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396068 | AATAGGGTTTGTGTT[-/C]CTATAAGAATCTAAT | 51434 |
rs746222719 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390918 | AATTATTGGCCGGGC[A/G]CAGTGGTTCACACCT | 51434 |
rs746236548 | snp | C/G | 1.6577e-05 | 0.00287893 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396397 | CCTTATCATGAAAGA[C/G]AGAATCTGCATGATA | 51434 |
rs746263951 | snp | C/G | 3.44003e-05 | 0.00414716 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396500 | TCCTCCCTTTCAATC[C/G]AAGCTCCCCCAGCTT | 51434 |
rs746278576 | snp | A/C/T | 0.00023374 | 0.0108081 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381964 | CTGGAGAAAAAAAAA[A/C/T]AAAAAAAAACACAAA | 51434 |
rs746298493 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404229 | ATTCCCTAGATCCGT[A/G]GAAATAAAGGCTGGA | 51434 |
rs746316741 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388818 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51434 |
rs746627163 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396888 | TACAGAGAAACCTCA[A/C]CACTTTGAATCCTTT | 51434 |
rs746724334 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377523 | GGCTAAAAGGGTAAG[G/T]GTCTGTGCATTTGCT | 51434 |
rs746812107 | snp | C/T | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375568 | CATTTAACCCTCATT[C/T]GATCATTTAATATCT | 51434 |
rs746820496 | in-del | -/AGA | 1.66174e-05 | 0.00288243 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382968 | ATCCATTCCTAGAAG[-/AGA]AGGACATAGTGAGAA | 51434 |
rs746848750 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381460 | TCCTGCTTCAGCCTC[C/T]CAAGTAGCTGGGACT | 51434 |
rs746866672 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403298 | GCCTCTGCCTTCTAT[A/G]TCTCCAAGCCGCCGC | 51434 |
rs746900196 | snp | C/T | 6.59239e-05 | 0.00574087 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387789 | GTGCACAAAAGCATA[C/T]GCTTTGATCCACACA | 51434 |
rs746902230 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374551 | TTTTTAGAGTTCTCA[A/G]TTTGAGTTTTTCTCC | 51434 |
rs746902256 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389216 | AAAAGACGCTGCCCT[C/T]TGGAAACTGGAATAA | 51434 |
rs746908544 | in-del | -/AAA | 0.00694533 | 0.0585186 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396226 | CTTGGAGTCTTTCTC[-/AAA]AAAAAAAAAAAAAAA | 51434 |
rs746953116 | snp | A/G/T | 3.55753e-05 | 0.00421742 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374375 | GCCTGAATCTCTGCC[A/G/T]TGCTCTTGCTGGCTG | 51434 |
rs746953510 | snp | A/C | 1.65886e-05 | 0.00287993 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388466 | ATTGAGAACTACTAT[A/C]TTTGACAGTAAACAT | 51434 |
rs746987162 | snp | C/T | | | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401414 | CACTGCGCTTTCAAT[C/T]GGTGGGTGATGCGAA | 51434 |
rs747009521 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402723 | AGGCGCCACGCCCAC[C/G]CATTAATGGAGTCTC | 51434 |
rs747048670 | snp | A/G | | | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401427 | ATTGGTGGGTGATGC[A/G]AAGGGTAGAAAAGTG | 51434 |
rs747063653 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376919 | CAAGGTCAGGATTTC[G/T]AAACCGGCCTGGCCA | 51434 |
rs747082495 | snp | A/G | 1.72636e-05 | 0.00293794 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388673 | CGTATATTGCAAAGA[A/G]AATCTCTCACCATGA | 51434 |
rs747157447 | snp | A/G | 6.59076e-05 | 0.00574016 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374264 | CTCCTCCTGAGTGGC[A/G]TCCGTGGGACTCTCC | 51434 |
rs747227682 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400023 | TTGAACCCAGCAGGC[A/G]GAGGTTGCAGTGAGC | 51434 |
rs747313898 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379807 | GAGGAACTGCATCTT[C/G]TAAGATCTATTTTAA | 51434 |
rs747383292 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382921 | TCAACATCCTCTAGC[C/T]GCCCTTCTCGTGCCA | 51434 |
rs747435205 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391750 | TTATGAAGGAGATTA[C/T]GGTATATTTCTAATA | 51434 |
rs747568516 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405575 | ATGTTTTTCAGGGCT[C/G]CTTCAAGTGGGATTG | 51434 |
rs747625247 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376708 | CATAAATCAGGACTG[-/A]AAAAAAAAAAAAAGG | 51434 |
rs747628664 | snp | C/T | 3.82431e-05 | 0.00437265 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403550 | ATTACTCATTGTAAG[C/T]AACAAGCTGCTGAGG | 51434 |
rs747671702 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385885 | TTTTTCAAGATCAGT[A/G]ATTTTTCTGTTGTTC | 51434 |
rs747751155 | snp | A/C | 3.33328e-05 | 0.00408231 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403643 | CCTGCTCTGCAAAGC[A/C]GCGGGCAGCGGCGGC | 51434 |
rs747759235 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384743 | ACCTACCTCACAATT[C/T]GAAAGCCTGCTATTT | 51434 |
rs747810245 | snp | C/G | 1.64811e-05 | 0.00287059 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386286 | TATCTCTGATCCCCC[C/G]CAACAACAGCCACTG | 51434 |
rs747810973 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401951 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs747882093 | snp | A/G | 8.27109e-05 | 0.00643029 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388485 | GACAGTAAACATGCC[A/G]TGAAAACAGGCAGGA | 51434 |
rs747915895 | in-del | -/TC | 0.000150357 | 0.00866925 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396244 | AAAAAAAAAAAAAAA[-/TC]ACAATTCTATCTCCA | 51434 |
rs748016515 | snp | A/G | 1.65553e-05 | 0.00287705 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388634 | TTTATCTGTACAAAC[A/G]CAAATAACAGATAGC | 51434 |
rs748017065 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398739 | AAGGTGGGTGGATCA[C/T]CTAAGTTCAGGACCT | 51434 |
rs748088234 | snp | C/G | | | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377705 | CTCCAAATTGCTAAC[C/G]TTCAAAGTTTCAGAC | 51434 |
rs748151069 | in-del | -/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403464 | CCCACGTGCCCTGAG[-/C]CCCCGCTCCCAGACC | 51434 |
rs748155382 | snp | C/T | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375875 | AACAGTTCTCTAATG[C/T]TGTTAATATATTTTA | 51434 |
rs748181414 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389298 | TCTTAAAACAGAAGA[C/T]GAACTATCTCACATA | 51434 |
rs748238077 | snp | A/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403941 | ACTACTCGGTCAATT[A/T]GAATGAGTCTGAGAG | 51434 |
rs748243736 | snp | A/C | 3.53182e-05 | 0.00420213 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396245 | AAAAAAAAAAAAAAT[A/C]ACAATTCTATCTCCA | 51434 |
rs748298890 | snp | A/G | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381782 | AGCGACAAGGTGCGA[A/G]CCGTATGGCCTCCCG | 51434 |
rs748329774 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402862 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACCGCA | 51434 |
rs748460716 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391055 | ATTAGGCAGGTGCAG[C/T]GGTACGCGCCTGTAG | 51434 |
rs748507511 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386418 | GTACAGATCTGCCAA[A/G]CTTCCCAATAGGTCC | 51434 |
rs748508339 | snp | C/T | 3.47343e-05 | 0.00416725 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374137 | CGGCCATGGAGCTGC[C/T]GCCCCCTCACTGCAT | 51434 |
rs748604434 | snp | A/G | 3.30644e-05 | 0.00406585 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395191 | ACATTCAGCCATTTT[A/G]TATTTCACTTCAATT | 51434 |
rs748627493 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379896 | GGGTCAATTCACATG[A/G]ACTTAAAATATTACA | 51434 |
rs748741438 | snp | A/C | 2.00298e-05 | 0.00316457 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403697 | GAGGATCCTTAGGGA[A/C]GACTCCAAAATGGCG | 51434 |
rs748783622 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386299 | CCCCAACAACAGCCA[C/T]TGTCTTCCTGCCCCA | 51434 |
rs748792115 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386429 | CCAAGCTTCCCAATA[A/G]GTCCACGTTATCTCG | 51434 |
rs748820672 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373990 | GTTTTAGAAATGAAG[C/T]CACGACTAGGAATTG | 51434 |
rs748864802 | in-del | -/TAA | 1.64741e-05 | 0.00286998 | cds-indel, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377457 | GGTCAGGGCTTTATC[-/TAA]TAATGTTTTGGCTTT | 51434 |
rs748871984 | in-del | -/AAAC | 0.000535942 | 0.016361 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381970 | AAAAAAAAAAAAAAA[-/AAAC]AAACACAAAAACCCC | 51434 |
rs748872654 | in-del | -/CT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383566 | CAATATGGTGAGACC[-/CT]GTCTCTAAAGAAATT | 51434 |
rs748912487 | snp | A/G | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372699 | GCCCGGTTAATTTTT[A/G]TATTTTTAACAGAGC | 51434 |
rs748942760 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387957 | TCCACATGCAAGGAG[A/C]AACGGGCTACATCTT | 51434 |
rs748963334 | snp | C/G/T | 3.42063e-05 | 0.00413548 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374143 | TGGAGCTGCCGCCCC[C/G/T]TCACTGCATGCCGAA | 51434 |
rs749047737 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400024 | TGAACCCAGCAGGCG[C/G]AGGTTGCAGTGAGCC | 51434 |
rs749160446 | snp | A/G | 1.72344e-05 | 0.00293546 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377649 | ACGTGAAGACATTCA[A/G]TGCCATTACCATTCC | 51434 |
rs749261920 | snp | A/C/G | 1.68062e-05 | 0.00289877 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403649 | CTGCAAAGCCGCGGG[A/C/G]AGCGGCGGCAGCACT | 51434 |
rs749317348 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378471 | CTTAGGGAGAAAGAC[A/T]CTTTTATTTGAAACG | 51434 |
rs749343138 | snp | A/G | | | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377804 | GTGCTCTTCCCCAGA[A/G]AACTTGATGGATGTA | 51434 |
rs749370734 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391557 | TGTTTGAGGCACACA[C/T]CTTTGCTCCTAGCTG | 51434 |
rs749383338 | snp | A/G | 0.000302893 | 0.0123026 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381960 | ACAGCTGGAGAAAAA[A/G]AAAAAAAAAAAAACA | 51434 |
rs749408620 | in-del | -/AGAGAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387234 | GAGAGAGAGAGAGAG[-/AGAGAC]AGAGAGACAGAGAGA | 51434 |
rs749415801 | snp | C/T | | | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386445 | GTCCACGTTATCTCG[C/T]AATAAGGATTTTTTC | 51434 |
rs749468985 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381114 | ACCAGAAAAAAAATC[A/T]GAAAAAATGGATTAT | 51434 |
rs749475167 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390666 | GGCCTCAGATTTTCC[A/G]TATTAGGCTACTATT | 51434 |
rs749732210 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393346 | TATTTCCTATAATAA[A/G]AAATATCAAAGTCTT | 51434 |
rs749772145 | snp | C/T | 1.65157e-05 | 0.0028736 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396271 | CTCCAATTACCTGAC[C/T]TTGTGGAGTAGATGC | 51434 |
rs749774380 | snp | A/G | 1.65493e-05 | 0.00287652 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381829 | TCTTGGACTCTGCCC[A/G]TGTTCCTAAGTGCTG | 51434 |
rs749816901 | snp | A/G | 4.96422e-05 | 0.00498183 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396389 | CCGATATTCCTTATC[A/G]TGAAAGAGAGAATCT | 51434 |
rs749880586 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378180 | GCTCACTGCAATCTC[C/T]GCCTCCCGGGTTCAA | 51434 |
rs749918487 | in-del | -/CA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387234 | AGAGAGAGAGAGAGA[-/CA]GAGACAGAGAGACAG | 51434 |
rs749922810 | snp | A/C | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377349 | CTGAGGTCAGGTTTT[A/C]TAAAAATTAATGATG | 51434 |
rs749985145 | snp | G/T | 3.7386e-05 | 0.00432338 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387942 | GCACGATATCTCTCT[G/T]CCACATGCAAGGAGC | 51434 |
rs750063065 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388578 | TGGTGACTGAAGGGC[A/G]CTCCTGACCAGCCTT | 51434 |
rs750135941 | in-del | -/CACAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392090 | AGCAAGACTCCACCT[-/CACAA]AAAAAAAAAAAAAAA | 51434 |
rs750222106 | snp | C/T | 8.24178e-05 | 0.00641889 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396326 | TTTTGAAGTTTTACT[C/T]AGCGCTTTCTTCTGC | 51434 |
rs750264243 | snp | A/G | 0.000223714 | 0.0105739 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381953 | AGCTGTGACAGCTGG[A/G]GAAAAAAAAAAAAAA | 51434 |
rs750293481 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385500 | CATTGCCATTCCAAG[C/T]TGCCAGCTGTTGCCA | 51434 |
rs750337645 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381146 | AAAGTATGGGGTGAC[A/G]AATCCAGTGAAAGCC | 51434 |
rs750413054 | in-del | -/AGAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387244 | GAGAGAGAGACAGAG[-/AGAC]AGAGAGACAGAGAGA | 51434 |
rs750459818 | snp | A/C/G | 8.30255e-05 | 0.0064425 | missense, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403670 | CGGCAGCACTGACTC[A/C/G]AAAAGCCGGTAGAGG | 51434 |
rs750521717 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395367 | TTGCCCAGGCTGCAA[C/T]GCAGTGGTGCAAACA | 51434 |
rs750575361 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386323 | TGCCCCAAGAATTAC[C/T]TACCTTTTATCAGAT | 51434 |
rs750683112 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377387 | CAGAAAATAAGACAC[A/G]CTTACTAAGTAGTTC | 51434 |
rs750689017 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373457 | TTGAAAAGGGCTTCC[A/C]TTCTGATCACCCCAA | 51434 |
rs750761717 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392776 | TAAACTCAAACTAGA[A/C]ACCAGATCTTTTTTT | 51434 |
rs750775202 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387090 | ACAAAAATTAGCTGG[A/G]TGTGGTGGCATGCGC | 51434 |
rs750842457 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382368 | TTTTCCAAATGAGAA[C/T]ACAGACCTAGATAGG | 51434 |
rs750854289 | snp | A/G | 3.29544e-05 | 0.00405908 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377604 | GTTGGAGGCTAAGTA[A/G]CATTCGATAAGACCT | 51434 |
rs750906887 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400780 | GCTGGGCTCGGTGGC[C/T]CACGCCTGCAATCCA | 51434 |
rs750909603 | snp | C/G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385793 | CCTTATTTCCCACTA[C/G/T]TCCTGAGAACTCACT | 51434 |
rs750996175 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399890 | CACCTGAGGTCAGGA[C/G]TTCGACCAGCCTGGC | 51434 |
rs751109154 | snp | C/T | 6.59609e-05 | 0.00574248 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388614 | ACAGGTTTGCCAGCA[C/T]CATGTTTATCTGTAC | 51434 |
rs751154745 | in-del | -/AC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376447 | GTGGCAGGTGCCTGT[-/AC]AGTCCCAGCTACTCG | 51434 |
rs751162576 | snp | A/G | 1.68049e-05 | 0.00289865 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395063 | AGGGAGCAGGGTTAG[A/G]AGAGCTGAGGAGAAA | 51434 |
rs751164186 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377427 | CACCACAGCCTTAAT[A/G]TAATCTGGCCTTTGG | 51434 |
rs751242086 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376918 | ACAAGGTCAGGATTT[C/T]GAAACCGGCCTGGCC | 51434 |
rs751287017 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377613 | TAAGTAACATTCGAT[A/G]AGACCTGAAAAAAGT | 51434 |
rs751324036 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391356 | GGTGAAGATTTACCA[A/G]GATTTAATAATCTAA | 51434 |
rs751372073 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404644 | ATTTTTACAGTAGTA[C/G]ATGCAAAAAAAATGC | 51434 |
rs751413690 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390030 | GTGATAAAAGACCTT[C/T]CTAATAGTACACAGA | 51434 |
rs751439107 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405225 | ATTCTAAGGGGGTCC[A/G]CGTGAGAGAGTCGTG | 51434 |
rs751466144 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372524 | GTGACCCCAACTATC[C/T]GTGGGGCTTTATTTT | 51434 |
rs751525641 | snp | A/G | 1.66818e-05 | 0.00288802 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386507 | TGAACCTTTAAATCT[A/G]TTATAAATCCTCTTA | 51434 |
rs751529559 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383109 | CACAGGCTCCTCCAA[C/T]TACTATTTCCAGTTT | 51434 |
rs751646812 | snp | A/C | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374234 | TTCCCCACTCCCTTC[A/C]ATGTCGTCCACATCC | 51434 |
rs751790732 | snp | A/C | 1.7617e-05 | 0.00296786 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396232 | GTCTTTCTCAAAAAA[A/C]AAAAAAAAAAATCAC | 51434 |
rs751795804 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395490 | AAAGACAGGGGTCTC[A/G]CTATGTTGCCAAGGC | 51434 |
rs751929988 | in-del | -/G | 5.84778e-05 | 0.00540699 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381963 | CTGGAGAAAAAAAAA[-/G]AAAAAAAAAACACAA | 51434 |
rs751956453 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374871 | GACCCAAGGCTACCC[C/T]TACCCAAGCATTCAC | 51434 |
rs751974146 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402244 | TAGAGAGCAGTGAAC[A/G]GAGTAATGAGATGAA | 51434 |
rs751990385 | in-del | -/CAAAAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384397 | CCCTGTCTCTAACAA[-/CAAAAC]CAAAACCAAAACCAA | 51434 |
rs752016031 | in-del | -/AGAA | 1.72469e-05 | 0.00293652 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387903 | CAAGCCTAAACCAAC[-/AGAA]AGCAGAAGAAAGAAA | 51434 |
rs752128175 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386372 | CCTGTTCAAACTTGA[A/G]GACAGAGTTTTTATT | 51434 |
rs752152085 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400984 | GAGCCTGGGAGGTGG[A/G]GGCTGTAGTCAGCCG | 51434 |
rs752163086 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401682 | GATCACCAGAGGTCA[A/G]GAGTTGAAGACCAGA | 51434 |
rs752187264 | snp | C/T | 1.72065e-05 | 0.00293308 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395257 | TCTTTGAAACGTTAT[C/T]CCAACAATATGACAG | 51434 |
rs752188441 | snp | A/T | 1.65669e-05 | 0.00287805 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377628 | AAGACCTGAAAAAAG[A/T]AAAACACGTGAAGAC | 51434 |
rs752310239 | snp | C/T | 1.75517e-05 | 0.00296236 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381737 | CACACCATTCACCTA[C/T]GTTTTCTTTCTTACC | 51434 |
rs752460830 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378283 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 51434 |
rs752471810 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379284 | AAAAACAGAATGCAC[G/T]TGCCTAACCTAAATC | 51434 |
rs752503841 | snp | G/T | 5.3312e-05 | 0.00516267 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374111 | AGTGCTCAGAGCAGG[G/T]CAGGCCACTGCGGCC | 51434 |
rs752565406 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392321 | ATCATACTGAAGAAA[C/T]AGCTTCAAAAACTCA | 51434 |
rs752599830 | snp | A/C | 1.66949e-05 | 0.00288915 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395082 | GCTGAGGAGAAAAAC[A/C]CATAAACATTCAACT | 51434 |
rs752641209 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392057 | AGATTGTGCCACTGC[A/C]CTCCAGCCTGGCAAC | 51434 |
rs752662978 | snp | A/C/T | 3.29534e-05 | 0.00405904 | synonymous-codon, missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376104 | CATTGCCTCCTGATA[A/C/T]TCATTGACAGCTACA | 51434 |
rs752694872 | snp | A/C | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404944 | CCCTGCCTCAGCTTC[A/C]CGAGTAGCTGGGATT | 51434 |
rs752884167 | snp | A/G | 0.0419331 | 0.138594 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381957 | GTGACAGCTGGAGAA[A/G]AAAAAAAAAAAAAAA | 51434 |
rs753022552 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398044 | GAAGGTTGGGAGTTT[C/G]AGACTAGCCTGGCCA | 51434 |
rs753036966 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381586 | ATGATCTGCCCGTCT[C/T]GGCCTCCCAAAGTGC | 51434 |
rs753109984 | snp | A/C | 1.67276e-05 | 0.00289197 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386513 | TTTAAATCTATTATA[A/C]ATCCTCTTAGTTGCT | 51434 |
rs753143306 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394189 | CAAAACAAAAAAAAC[-/A]AAAACAAAAATAAAA | 51434 |
rs753190006 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398074 | AATAAGGTGAAACCC[C/T]GTCTCTAGTAAAAAT | 51434 |
rs753234725 | snp | C/T | 4.99297e-05 | 0.00499623 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387870 | TGCCACCTCTGCCCC[C/T]TTTACAGAAAGGGAC | 51434 |
rs753267092 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375076 | TTATTTTCTCACTTG[C/T]TTCTGAGATTCTAAA | 51434 |
rs753319774 | snp | A/G | 1.72359e-05 | 0.00293558 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381879 | TTGAACACTATTACT[A/G]TTCAGCTGAATGGCC | 51434 |
rs753479201 | snp | A/T | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375402 | ATTGAATGTGATCAG[A/T]CTCTATTAAAGACAG | 51434 |
rs753588844 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401147 | ACTTTTCCCTTCTGA[C/T]CTAGACCAGCTTCTA | 51434 |
rs753594888 | in-del | -/AC | 8.35848e-05 | 0.00646416 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395080 | GAGCTGAGGAGAAAA[-/AC]ACATAAACATTCAAC | 51434 |
rs753686130 | snp | A/G | 1.75644e-05 | 0.00296342 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395272 | TCCAACAATATGACA[A/G]TTCTTCAAAACGTTA | 51434 |
rs753687507 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380252 | GCTACTCAGGAGGCT[A/G]AAGCAGGAGAATCAC | 51434 |
rs753699254 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389654 | CTAAAAGTTCTGGCC[A/G]GGCGCAGTGGCTCAT | 51434 |
rs753753946 | snp | C/T | 1.69487e-05 | 0.00291103 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381746 | CACCTATGTTTTCTT[C/T]CTTACCTTCATAACA | 51434 |
rs753757514 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394952 | TGGATTTTCAGGGTC[C/G]CCCACCCCCACTCCA | 51434 |
rs753808928 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396317 | AGGTCTCACTTTTGA[A/G]GTTTTACTTAGCGCT | 51434 |
rs753843631 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392582 | ATGAGCAAGGCAGGA[A/G]ACATGACAGTATTAT | 51434 |
rs753886608 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384632 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 51434 |
rs753925448 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382647 | CGATCTTGGCTCACT[A/G]CAACCTCTGCCTCCT | 51434 |
rs753952124 | snp | A/G | 0.000168705 | 0.00918282 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396472 | AAAACAAGAGAAAAT[A/G]TAATACATCTTTTCC | 51434 |
rs754001701 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373258 | AGCTGAAATCTGGCC[A/G]AAGACTCTCAGGCTC | 51434 |
rs754007870 | snp | A/G | 3.23934e-05 | 0.00402438 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403613 | CATGTCCCGCACGTG[A/G]TCTATCACATTCATC | 51434 |
rs754021937 | snp | A/T | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382875 | TTCTGCATGCTGATC[A/T]GAGATATTGAAAAGG | 51434 |
rs754086982 | snp | A/G | 1.73498e-05 | 0.00294527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387904 | AAGCCTAAACCAACA[A/G]AAAGCAGAAGAAAGA | 51434 |
rs754117400 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373517 | GGGAACTGCCCCAGG[C/T]GCACCTCTGGTTCAT | 51434 |
rs754148483 | snp | C/G | 1.67167e-05 | 0.00289103 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382989 | ACATAGTGAGAAGAG[C/G]TGTTTTAAGAAGAGA | 51434 |
rs754160625 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399646 | ATTGCATTATTGTGG[C/G]CATGTGCGGTGGCTT | 51434 |
rs754198690 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397581 | AAAAAAACACTAAAA[A/G]CTAAAGAAAATGCCA | 51434 |
rs754265266 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383549 | TTCAAGACCAGCCTG[A/G]GCAATATGGTGAGAC | 51434 |
rs754314981 | snp | A/G | 1.6681e-05 | 0.00288794 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377374 | ATGATGAACAGGACA[A/G]AAAATAAGACACACT | 51434 |
rs754506470 | snp | C/T | 1.67775e-05 | 0.00289629 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395069 | CAGGGTTAGGAGAGC[C/T]GAGGAGAAAAACACA | 51434 |
rs754542204 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398331 | TAAGACAGGACAATC[A/G]CTTGAGCCCAGGAGA | 51434 |
rs754616050 | snp | C/T | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375752 | AAGAAGAATATAAAA[C/T]ATATACTAGGTACAG | 51434 |
rs754745865 | in-del | -/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392092 | CAAGACTCCACCTCA[-/C]AAAAAAAAAAAAAAA | 51434 |
rs754769469 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400885 | AACCCCATCTCTATT[-/A]AAAAAAAAAAAAAAA | 51434 |
rs754878727 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390074 | CCAATTTAAAATTAG[A/G]TTTTTTTTTTTGAGA | 51434 |
rs754973840 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403825 | CTGTCGTGGTCCTTT[C/T]CAGGTGAAATGAGTT | 51434 |
rs754976723 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383130 | TTTCCAGTTTCCTAC[A/G]AAGTGACTATTAAAA | 51434 |
rs754991275 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402754 | CCGTTTCCTTTTTTT[C/G]AGACAGGCAGTCGTT | 51434 |
rs755099459 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381423 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 51434 |
rs755158061 | snp | A/G/T | 0.000115942 | 0.00761308 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396244 | AAAAAAAAAAAAAAA[A/G/T]CACAATTCTATCTCC | 51434 |
rs755195184 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381334 | GGATGATGTTTTTTT[-/G]TTGTTGTTGTTGTTG | 51434 |
rs755224326 | snp | C/T | 0.00013187 | 0.00811895 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396329 | TGAAGTTTTACTTAG[C/T]GCTTTCTTCTGCTGT | 51434 |
rs755248162 | snp | C/T | 8.28164e-05 | 0.00643439 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381779 | CTAAGCGACAAGGTG[C/T]GAGCCGTATGGCCTC | 51434 |
rs755299232 | in-del | -/AAAAC/AAAACAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381969 | AAAAAAAAAAAAAAA[-/AAAAC/AAAACAC]AAAACACAAAAACCC | 51434 |
rs755361929 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395516 | AAGGCTAGTCTCAAA[C/T]TCCTGACCTCAAGTC | 51434 |
rs755379887 | snp | G/T | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386386 | AGGACAGAGTTTTTA[G/T]TGTCTCCAGCTCTGA | 51434 |
rs755468041 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394044 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTGTAATCC | 51434 |
rs755502745 | snp | C/T | 1.74382e-05 | 0.00295276 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374134 | CTGCGGCCATGGAGC[C/T]GCCGCCCCCTCACTG | 51434 |
rs755560278 | snp | C/T | 1.70577e-05 | 0.00292037 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381742 | CATTCACCTATGTTT[C/T]CTTTCTTACCTTCAT | 51434 |
rs755697659 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385902 | TTTTTCTGTTGTTCA[C/T]GCCTAATTACTGCCT | 51434 |
rs755727221 | in-del | -/A | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375587 | CATTTAATATCTAAT[-/A]AGGTAGCTAGATATA | 51434 |
rs755730846 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401035 | AGCCTGGGCAACAAA[A/G]CAAGACTCCGTCTGA | 51434 |
rs755751593 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399940 | CTCTACTAAAAATAC[A/G]AAAATTAGCCAGGCA | 51434 |
rs755822389 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386425 | TCTGCCAAGCTTCCC[A/G]ATAGGTCCACGTTAT | 51434 |
rs755860246 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379301 | GCCTAACCTAAATCT[C/T]TACCAGCAAAAGAAG | 51434 |
rs755894547 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388642 | TACAAACACAAATAA[C/G]AGATAGCAAAATAAG | 51434 |
rs756023368 | snp | A/G | 6.65668e-05 | 0.00576879 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395090 | GAAAAACACATAAAC[A/G]TTCAACTTACTTTGG | 51434 |
rs756025557 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378312 | TTGGTCAGGCTGCTC[A/T]CGAACTCCTGACCTC | 51434 |
rs756144574 | snp | C/T | 1.67214e-05 | 0.00289144 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377635 | GAAAAAAGTAAAACA[C/T]GTGAAGACATTCAAT | 51434 |
rs756243601 | snp | A/C | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404087 | ACCTAACGGCCTTTA[A/C]AGTGGCGCATGCGCA | 51434 |
rs756285136 | snp | C/T | 1.65329e-05 | 0.0028751 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396383 | AGCATTCCGATATTC[C/T]TTATCATGAAAGAGA | 51434 |
rs756339658 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400850 | TCAGGAGTTCCAGAC[A/G]AGCCTGGCCAACATG | 51434 |
rs756357916 | snp | A/G | 0.00013314 | 0.00815797 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382836 | AAAAGAGAATGCATA[A/G]TCATACCCAGAAACC | 51434 |
rs756448703 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383294 | ATACAAAAAATTAGC[C/T]GGGCATAGTGGCACG | 51434 |
rs756449067 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392915 | ATTCTCCTGCCTCAG[C/T]CTCCAGAGTAGCTGA | 51434 |
rs756492320 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398109 | AAATTAGCCAGGTGC[A/G]GTGGCGAGTGCCTGT | 51434 |
rs756538413 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381676 | TTTGGGAAGTGCTGG[A/C]CTAATGAAACCTTCC | 51434 |
rs756564830 | snp | A/G | 3.32209e-05 | 0.00407546 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374321 | TAGAGACTTCTGGTC[A/G]TTGGGGTCCAAACTA | 51434 |
rs756628403 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396301 | CAGAATTTCCAGTTG[A/G]AGGTCTCACTTTTGA | 51434 |
rs756775406 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375108 | AGCAGCTAAAACCCA[C/T]GTTGGCACCGTTTCT | 51434 |
rs756804998 | snp | C/T | 1.67784e-05 | 0.00289636 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387705 | AGACAAGCAAAGGGC[C/T]TCAAGAACACTGAAT | 51434 |
rs756834403 | in-del | -/AAC | 6.82384e-05 | 0.00584077 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381971 | AAAAAAAAAAAAAAA[-/AAC]AACACAAAAACCCCA | 51434 |
rs756863104 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388797 | AAAAGAAAGAAGAAA[C/T]TGGCCAGGTGCAGTG | 51434 |
rs756894970 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387960 | ACATGCAAGGAGCAA[C/T]GGGCTACATCTTCCC | 51434 |
rs756901586 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392669 | AAGTAACAGAAAAAA[A/T]ACTATTCTTCTCATT | 51434 |
rs756958004 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383028 | TCCCACATACAGGAG[C/T]AGCACCCAACATCAG | 51434 |
rs756974166 | in-del | -/AGAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384233 | AAAGTAAAATAAAAT[-/AGAA]AGAAAAAAAAATTAG | 51434 |
rs756974249 | snp | A/T | 1.72701e-05 | 0.0029385 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377650 | CGTGAAGACATTCAA[A/T]GCCATTACCATTCCA | 51434 |
rs757004344 | snp | A/G | 1.81125e-05 | 0.00300931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387931 | AAGAAAGTAAGGCAC[A/G]ATATCTCTCTTCCAC | 51434 |
rs757004730 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402495 | CCACCACGCCTGGCT[A/G]AATTTTTTTGGTATT | 51434 |
rs757019826 | snp | C/T | 7.10139e-05 | 0.00595835 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396222 | AATTCTTGGAGTCTT[C/T]CTCAAAAAAAAAAAA | 51434 |
rs757083812 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401206 | GAGTAAAAGTTTCCA[C/T]TATAACGCCATTTGG | 51434 |
rs757111583 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405233 | GGGGTCCGCGTGAGA[C/G]AGTCGTGATCGATTG | 51434 |
rs757126058 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380286 | AACCCGGCAAGTGGA[C/G]GTTGCAGTGAGCTGA | 51434 |
rs757172491 | snp | C/T | 3.34381e-05 | 0.00408876 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381757 | TCTTTCTTACCTTCA[C/T]AACAATCTAAGCGAC | 51434 |
rs757214314 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379389 | CCTAAATCTCCAAAT[A/G]GCAGCTTAAGAAGCC | 51434 |
rs757238111 | in-del | -/TTAAG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400275 | CTACTTACACATGCA[-/TTAAG]TTATCTCTGTAATGA | 51434 |
rs757263211 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382082 | CCACACTTATAGTTT[-/T]AACCTAAGATATTAG | 51434 |
rs757306388 | in-del | -/TG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400158 | GTTCTCTTCAAACTC[-/TG]TGATTCTATGTATGT | 51434 |
rs757387660 | snp | A/G | 3.32198e-05 | 0.00407539 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403617 | TCCCGCACGTGGTCT[A/G]TCACATTCATCCTGC | 51434 |
rs757389587 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391645 | GCTCTAAGAATGATG[A/G]CAATGAAAATCAAGC | 51434 |
rs757598375 | snp | A/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376131 | TACAAGGAAATCTCC[A/T]AGGATCCGATGCAGG | 51434 |
rs757626468 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385545 | AAACATCATTTTCAT[C/G]ATGGGTGCAGGCAGC | 51434 |
rs757711630 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378530 | AGGGCTTCCCTAAAC[A/G]AGATGAACAGTACTT | 51434 |
rs757734149 | in-del | -/GA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387216 | CACTCTAGCCTGGGA[-/GA]GAGAGAGAGAGAGAG | 51434 |
rs757767691 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380771 | CATCCTGGCTAGCAC[A/G]GTGAAACACTGTCTC | 51434 |
rs757779045 | snp | C/T | 1.65499e-05 | 0.00287657 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396390 | CGATATTCCTTATCA[C/T]GAAAGAGAGAATCTG | 51434 |
rs757877857 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389793 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT | 51434 |
rs757903615 | snp | A/C | 1.65375e-05 | 0.0028755 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396491 | TACATCTTTTCCTCC[A/C]TTTCAATCCAAGCTC | 51434 |
rs757928328 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376173 | CTGATTAGCCAGTGC[A/G]TTCCTCAGCAAAGCA | 51434 |
rs757959144 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388552 | GCACTGCCTCAGCAC[C/T]TCCTTATAGCTGGTG | 51434 |
rs758009768 | snp | C/T | 3.75291e-05 | 0.00433164 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387943 | CACGATATCTCTCTT[C/T]CACATGCAAGGAGCA | 51434 |
rs758016617 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375388 | CTGTGTGCTGAACAA[C/T]TGAATGTGATCAGAC | 51434 |
rs758064759 | snp | C/T | 1.648e-05 | 0.0028705 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388598 | TGACCAGCCTTCTTG[C/T]ACAGGTTTGCCAGCA | 51434 |
rs758118135 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402332 | AAGTGCAATAAAGGA[-/T]TTTTTTTTTTTTTTT | 51434 |
rs758133410 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377396 | AGACACACTTACTAA[C/G]TAGTTCTGCTTTTTT | 51434 |
rs758154741 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389979 | AAAAAAGCCAGAAAA[C/T]CTAAAAGTTCCTAAG | 51434 |
rs758243013 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389161 | CTTCCCTAAGAGGAA[A/T]GTCACATTACCTTCC | 51434 |
rs758330439 | snp | C/T | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402711 | AGGAAACATGAAAGG[C/T]GCCACGCCCACCCAT | 51434 |
rs758443883 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384696 | AAAACAAAAAAAAAC[-/A]AAAAAAAACAAAAAA | 51434 |
rs758445505 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392016 | GAATCGCTTGAACCC[-/G]GGGAGGTGGAGGTTG | 51434 |
rs758471066 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386343 | TTTTATCAGATAAGG[A/T]TCCAACATCTGTGCC | 51434 |
rs758513320 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396388 | TCCGATATTCCTTAT[C/T]ATGAAAGAGAGAATC | 51434 |
rs758547384 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379444 | GCTGTCCAAATATTA[C/T]AGGACGGACTATTCA | 51434 |
rs758640910 | snp | C/T | 1.75366e-05 | 0.00296108 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374128 | AGGCCACTGCGGCCA[C/T]GGAGCTGCCGCCCCC | 51434 |
rs758680090 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393382 | CCTATGGAGTAGCCA[C/T]TCTTTATTCCTTTAT | 51434 |
rs758681229 | snp | A/C | 3.2981e-05 | 0.00406071 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395128 | TTGTCTTGAAGGGAT[A/C]CCATCAAGTATAGCA | 51434 |
rs758778656 | snp | A/C | 1.65493e-05 | 0.00287652 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403628 | GTCTATCACATTCAT[A/C]CTGCTCTGCAAAGCC | 51434 |
rs758788374 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373661 | CATTGCAGAAGGAAG[C/T]AAGATTTACTAGGGA | 51434 |
rs758808945 | snp | C/T | 1.6922e-05 | 0.00290873 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403487 | CCCAGACCGCCGCCG[C/T]TTTCTCCTCAGCCCC | 51434 |
rs758883207 | snp | A/C | 3.29891e-05 | 0.00406122 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386281 | CCTATTATCTCTGAT[A/C]CCCCCCAACAACAGC | 51434 |
rs758884103 | in-del | -/AAGTG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378411 | GCTCCTAGAGTCTTA[-/AAGTG]AATTTACAGTTTGAC | 51434 |
rs759011423 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379930 | CAAAACAAAGTTGGA[A/C]CCTGATTGTGCCCAC | 51434 |
rs759068447 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394826 | ACTGTAGCCTGGGTG[A/C]CAGTGAGACTCTGTC | 51434 |
rs759123525 | snp | C/T | 3.2993e-05 | 0.00406145 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396284 | ACTTTGTGGAGTAGA[C/T]GCAGAATTTCCAGTT | 51434 |
rs759124363 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379959 | ACTCTGGAGGTCACA[A/T]TGAACAGACCCATTC | 51434 |
rs759217247 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379056 | TAGTAGAGATGGTAG[A/T]TCACCATGTTGGCTA | 51434 |
rs759250267 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401906 | GTGAACCCAGAAGGC[A/G]AAGCTTGCAGTGAGC | 51434 |
rs759280978 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392178 | TTCATCTGTGCAACA[A/C]GATTATTCTTGGAGT | 51434 |
rs759357903 | in-del | -/AC/AGAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387357 | GAGAGAGAGACAGAG[-/AC/AGAC]AGAGAGAGACAGAGA | 51434 |
rs759361572 | in-del | -/GAGA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381951 | AAGCTGTGACAGCTG[-/GAGA]GAGAAAAAAAAAAAA | 51434 |
rs759372550 | snp | G/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403654 | AAGCCGCGGGCAGCG[G/T]CGGCAGCACTGACTC | 51434 |
rs759408589 | snp | A/G | 1.77868e-05 | 0.00298213 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374108 | GGAAGTGCTCAGAGC[A/G]GGGCAGGCCACTGCG | 51434 |
rs759512682 | snp | C/T | 3.30066e-05 | 0.00406229 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387827 | AGTCCAAGTTAGGCA[C/T]GGTTTGGATCACATT | 51434 |
rs759639186 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376080 | CCTTAGTGCTATACT[A/G]TACTGGTCCATTGCC | 51434 |
rs759671095 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398837 | GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 51434 |
rs759763835 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397873 | ACACTCCAGCCTGGG[C/T]GACAAGAGTGAAACT | 51434 |
rs759801152 | snp | C/G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377898 | TGCAGCATGTGAGCA[C/G/T]CCCATCTGACCACTG | 51434 |
rs759818197 | snp | A/G | 1.66626e-05 | 0.00288635 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376249 | ACCCTCACTTAAGTC[A/G]TGTACAAAAAAACCA | 51434 |
rs759875383 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381058 | GAGCGGTGGGAGGAC[-/A]AAAAAAAAAAAACCC | 51434 |
rs759966133 | snp | G/T | 1.68422e-05 | 0.00290187 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381857 | CTGCTCCCTTAAGTA[G/T]CAGAGCTTGAACACT | 51434 |
rs760034349 | in-del | -/C | 0.000117364 | 0.00765952 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403749 | CCACACGCGGCACCA[-/C]CCCCCAAGCAAGAGG | 51434 |
rs760079349 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388762 | CCTGTGCAAATAAAG[A/G]CAGACTGACCCCATT | 51434 |
rs760134947 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403296 | GAGCCTCTGCCTTCT[A/G]TGTCTCCAAGCCGCC | 51434 |
rs760155593 | snp | C/T | 5.00956e-05 | 0.00500453 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386508 | GAACCTTTAAATCTA[C/T]TATAAATCCTCTTAG | 51434 |
rs760193445 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380902 | GAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCA | 51434 |
rs760198290 | snp | C/G | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396304 | AATTTCCAGTTGAAG[C/G]TCTCACTTTTGAAGT | 51434 |
rs760214385 | snp | A/C | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375245 | TGGACTCCCACCTTC[A/C]CTTCTACAGACTACT | 51434 |
rs760262629 | snp | A/C | 6.42901e-05 | 0.00566929 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381968 | AGAAAAAAAAAAAAA[A/C]AAAAACACAAAAACC | 51434 |
rs760339465 | snp | C/T | 3.43371e-05 | 0.00414335 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381874 | AGAGCTTGAACACTA[C/T]TACTGTTCAGCTGAA | 51434 |
rs760373488 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395875 | AATCAGCTATCATCT[A/G]AATCAGCGGTCCCCA | 51434 |
rs760411217 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380155 | CAGGAGTTCGGGACC[A/G]GCCTGGCTAACATGG | 51434 |
rs760487546 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374184 | TGGTCAGCCCACTGG[A/G]CCGCCTCACTGTCGC | 51434 |
rs760520067 | snp | C/T | 6.64308e-05 | 0.0057629 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386491 | GATATTTATTAAACA[C/T]TGAACCTTTAAATCT | 51434 |
rs760599811 | snp | A/G | 1.73237e-05 | 0.00294305 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395264 | AACGTTATTCCAACA[A/G]TATGACAGTTCTTCA | 51434 |
rs760625256 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378076 | GGTTTAAGATGGAAG[A/C]CTCCTAGGGTCTTTA | 51434 |
rs760786613 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377516 | AAACGGTGGCTAAAA[A/G]GGTAAGGGTCTGTGC | 51434 |
rs760792705 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404428 | TGTTAAATGGTTGAC[C/T]TGGAATCAGATCGAC | 51434 |
rs760918431 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385486 | AGATTCCAAGCTGCC[A/G]TTGCCATTCCAAGCT | 51434 |
rs761035176 | snp | A/C | 0.000187085 | 0.00966993 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403591 | TGGAGTGCAGCCCCG[A/C]GGCCGCCATGTCCCG | 51434 |
rs761178778 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388537 | ATCAAGGGCTAATGG[A/G]CACTGCCTCAGCACC | 51434 |
rs761372460 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396900 | CACCACTTTGAATCC[-/T]TTTTTAAAAACAGGC | 51434 |
rs761407750 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404477 | CGCAAACTCAAATGT[A/G]TACAGGGACCAGGGA | 51434 |
rs761507578 | in-del | -/ATTT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391439 | TATTAACAGACATTC[-/ATTT]AGACACATTTTGACT | 51434 |
rs761589851 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380997 | TCTTGCATGGTGTCT[A/G]ACACAGAGAGATTCA | 51434 |
rs761687318 | snp | A/C | 3.33195e-05 | 0.0040815 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376046 | TCAGTGGCCTTCCCC[A/C]AAGGGAGGCTAGTGC | 51434 |
rs761763728 | snp | A/C/G | 8.41466e-05 | 0.00648591 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395053 | ACATGGAGAGAGGGA[A/C/G]CAGGGTTAGGAGAGC | 51434 |
rs761767633 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397022 | TCCTGGCTAACGCGG[C/T]GAAACCCCATCTCTA | 51434 |
rs761934224 | in-del | -/T | 1.67269e-05 | 0.00289191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382992 | TAGTGAGAAGAGGTG[-/T]TTTAAGAAGAGAAGC | 51434 |
rs761987798 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374745 | ATTTCTCTGAGTATA[G/T]GTGTCCCATGTTCTT | 51434 |
rs761999222 | in-del | -/AAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | CTGTGACAGCTGGAG[-/AAA]AAAAAAAAAAAAAAA | 51434 |
rs762048752 | snp | A/G | 4.94295e-05 | 0.00497115 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388564 | CACCTCCTTATAGCT[A/G]GTGACTGAAGGGCGC | 51434 |
rs762069465 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391464 | ATTTTGACTCACTTC[C/G]TTGTCCTTTACATAG | 51434 |
rs762081472 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400738 | AAATGTGGGTCTCAC[C/T]AGTAAGGTCCAAAGC | 51434 |
rs762082179 | snp | A/C | 7.47692e-05 | 0.00611384 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403663 | GCAGCGGCGGCAGCA[A/C]TGACTCGAAAAGCCG | 51434 |
rs762124188 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382299 | CAGTACTAAGCACAA[C/T]GCATTCACCAACTCA | 51434 |
rs762145703 | snp | C/T | | | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401506 | ATCCAGGCTAAAACC[C/T]GAAGGAGGAGGCAAC | 51434 |
rs762157581 | in-del | -/ATCAGCTCAGTTTTT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389352 | AGCTAGTTAAGAAGG[-/ATCAGCTCAGTTTTT]CCTAATAAGGAAATG | 51434 |
rs762188234 | snp | A/C | 2.81235e-05 | 0.00374979 | missense, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403726 | CGGCGTCGCCGGGGT[A/C]CATCGGGTCCACACG | 51434 |
rs762256593 | snp | A/T | 1.66663e-05 | 0.00288667 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377375 | TGATGAACAGGACAG[A/T]AAATAAGACACACTT | 51434 |
rs762383009 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402316 | TGGGAAAGAATTTTC[A/G]TAAGTGCAATAAAGG | 51434 |
rs762432111 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378993 | CCTCCCAAGTAGCTG[G/T]GACTACAGGCGTGCA | 51434 |
rs762445223 | snp | G/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405618 | GGGAACCTAGAGTGG[G/T]AGAGATTAAGCTGAA | 51434 |
rs762539545 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391925 | GGTGAAACCCCGTCT[A/C]CACTAAAATGCAAAA | 51434 |
rs762641278 | in-del | -/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404740 | AGCTCCTGTAGATCC[-/T]TTTTCCCATCTCATC | 51434 |
rs762717273 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404600 | CTTAAAGGAGACAGT[C/T]GTTTTGGTCTAGATT | 51434 |
rs762751283 | snp | A/T | 0.000233672 | 0.0108065 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382984 | GAAGGACATAGTGAG[A/T]AGAGGTGTTTTAAGA | 51434 |
rs762759610 | snp | G/T | 3.09047e-05 | 0.00393083 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403581 | AGCCGCACGTTGGAG[G/T]GCAGCCCCGCGGCCG | 51434 |
rs762764075 | in-del | -/CAAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398948 | GCCAAACTCCATCTC[-/CAAAAA]CAAAAACAAAAACAA | 51434 |
rs762826034 | snp | A/G | 1.68383e-05 | 0.00290153 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382805 | ATTATCTCTTAATCT[A/G]CTGACAACTGGGGAG | 51434 |
rs762846112 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397673 | GACACCAAGGCAGGC[A/G]GATCACCTGAGGTCA | 51434 |
rs762881656 | snp | C/T | 1.66668e-05 | 0.00288672 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382977 | TAGAAGAGAAGGACA[C/T]AGTGAGAAGAGGTGT | 51434 |
rs762918560 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381219 | GTCTGCACATTGGTA[A/G]CCCCTGGGGACCTCC | 51434 |
rs762957344 | in-del | -/TT | 1.64741e-05 | 0.00286998 | frameshift-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386328 | CAAGAATTACTTACC[-/TT]TTATCAGATAAGGAT | 51434 |
rs763034314 | snp | C/T | 1.66338e-05 | 0.00288386 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386497 | TATTAAACATTGAAC[C/T]TTTAAATCTATTATA | 51434 |
rs763045259 | in-del | -/GTT | 5.26745e-05 | 0.00513171 | cds-indel, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403529 | CGCCTCAACTCACGG[-/GTT]GTTATTACTCATTGT | 51434 |
rs763131153 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389179 | CACATTACCTTCCCA[A/C]AAGGCCCAGTAATAT | 51434 |
rs763198405 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376360 | AAGCCCTATTCAGTT[A/G]AGAAATTTTCCATCC | 51434 |
rs763204221 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377609 | AGGCTAAGTAACATT[C/T]GATAAGACCTGAAAA | 51434 |
rs763213316 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389500 | GTACTAACTCACTAA[A/C]GTAATGCTACAAAAA | 51434 |
rs763239910 | snp | A/C | 3.29717e-05 | 0.00406015 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387801 | ATACGCTTTGATCCA[A/C]ACAGAGAGCCAGTCC | 51434 |
rs763272079 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374197 | GGGCCGCCTCACTGT[C/T]GCTGCCCTCCAGGTC | 51434 |
rs763296976 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378233 | CGAGTAGCTGGGATT[-/A]ACAAGCATGCACCAC | 51434 |
rs763381630 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401624 | GGCCAGAAGCGATGG[C/T]TCACGCCTGTAATCC | 51434 |
rs763386980 | snp | A/C | 3.41279e-05 | 0.00413072 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395243 | ACAATGGAAATATTT[A/C]TTTGAAACGTTATTC | 51434 |
rs763463380 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402125 | GGCTGCAGTGAGCCA[-/AG]ACTGCGCCACTCAAC | 51434 |
rs763476213 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403331 | GCCACATCCCCGCGG[G/T]ACTTGACGCCGGCAC | 51434 |
rs763538022 | snp | C/T | 1.7179e-05 | 0.00293074 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381875 | GAGCTTGAACACTAT[C/T]ACTGTTCAGCTGAAT | 51434 |
rs763751618 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380224 | GGTGTGGTGGTGTAT[A/G]CCTGTAATCCCAGCT | 51434 |
rs763785925 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404992 | CTGTCATGTGCGTCC[C/G]TGTGAAGAGACCACC | 51434 |
rs763795325 | in-del | -/AAAAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376568 | GCGAGACTCCATCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 51434 |
rs763920208 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394951 | CTGGATTTTCAGGGT[C/G]CCCCACCCCCACTCC | 51434 |
rs764008152 | snp | C/T | 5.22735e-05 | 0.00511214 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395267 | GTTATTCCAACAATA[C/T]GACAGTTCTTCAAAA | 51434 |
rs764028219 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392551 | CACAAGTTGCACAAA[A/C]CAGTTTTTCAATAAA | 51434 |
rs764063239 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396305 | ATTTCCAGTTGAAGG[C/T]CTCACTTTTGAAGTT | 51434 |
rs764089463 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395631 | AGAGTCTCGTTCTGT[C/T]ACCCAGGCTGGTGTC | 51434 |
rs764136297 | snp | C/T | 3.40096e-05 | 0.00412354 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381744 | TTCACCTATGTTTTC[C/T]TTCTTACCTTCATAA | 51434 |
rs764219174 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399022 | TGAGCTGAATAATTC[-/T]TTTTTTTTTTTTTTT | 51434 |
rs764237755 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373230 | AGCTGCAGCAAAAGA[A/G]CCAGGCAGACGCAGC | 51434 |
rs764265198 | snp | A/G | 5.01433e-05 | 0.00500691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382988 | GACATAGTGAGAAGA[A/G]GTGTTTTAAGAAGAG | 51434 |
rs764405314 | snp | C/T | 6.22142e-05 | 0.00557703 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403600 | GCCCCGCGGCCGCCA[C/T]GTCCCGCACGTGGTC | 51434 |
rs764418996 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398178 | TTGAACCCAGGAGGC[A/C]GAGGTTGGGGTGAGC | 51434 |
rs764442142 | in-del | -/AA/G | 0.00159574 | 0.0282015 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | TGTGACAGCTGGAGA[-/AA/G]AAAAAAAAAAAAAAA | 51434 |
rs764442525 | in-del | -/AAGA | 1.74033e-05 | 0.0029498 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387912 | ACCAACAGAAAGCAG[-/AAGA]AAGAAAGTAAGGCAC | 51434 |
rs764543170 | in-del | -/GCGC | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402130 | CAGTGAGCCAAGACT[-/GCGC]CACTCAACTCCAGCA | 51434 |
rs764584620 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376112 | CCTGATACTCATTGA[C/T]AGCTACAAGGAAATC | 51434 |
rs764610871 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391205 | AAACAAACAAACAAA[A/C]AAAGTCAACTATTTT | 51434 |
rs764881696 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404494 | ACAGGGACCAGGGAG[A/G]TAACTGAGCCAATGA | 51434 |
rs764885954 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398106 | AAAAATTAGCCAGGT[-/A]GCGGTGGCGAGTGCC | 51434 |
rs765033413 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396325 | CTTTTGAAGTTTTAC[C/T]TAGCGCTTTCTTCTG | 51434 |
rs765061710 | snp | A/T | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402509 | TAAATTTTTTTGGTA[A/T]TTTTTAAGCAGAGAC | 51434 |
rs765157994 | snp | C/G | 3.9265e-05 | 0.00443068 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396456 | GAGAATAACTCACTA[C/G]AAAACAAGAGAAAAT | 51434 |
rs765178921 | snp | A/C | 3.3451e-05 | 0.00408954 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403620 | CGCACGTGGTCTATC[A/C]CATTCATCCTGCTCT | 51434 |
rs765195191 | snp | A/C/T | 3.36991e-05 | 0.00410471 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382800 | CAACCATTATCTCTT[A/C/T]ATCTACTGACAACTG | 51434 |
rs765197462 | in-del | -/AAAA | 0.0213377 | 0.101062 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | CTGTGACAGCTGGAG[-/AAAA]AAAAAAAAAAAAAAA | 51434 |
rs765508712 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373405 | CTGGGGCTGAATCAA[A/T]GCATTGCGAATAAGA | 51434 |
rs765540184 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386319 | TTCCTGCCCCAAGAA[C/T]TACTTACCTTTTATC | 51434 |
rs765592628 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397557 | GCGAGATCTCGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs765592741 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388569 | CCTTATAGCTGGTGA[C/T]TGAAGGGCGCTCCTG | 51434 |
rs765593613 | snp | C/T | 1.75684e-05 | 0.00296376 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374126 | GCAGGCCACTGCGGC[C/T]ATGGAGCTGCCGCCC | 51434 |
rs765646006 | snp | C/T | 1.65734e-05 | 0.00287862 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377384 | GGACAGAAAATAAGA[C/T]ACACTTACTAAGTAG | 51434 |
rs765654625 | snp | A/G | 9.88403e-05 | 0.00702925 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377589 | TGCTTCTCGAATACT[A/G]TTGGAGGCTAAGTAA | 51434 |
rs765722574 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399695 | ACTTAGAGGCTGAGG[A/C]AGGAGAATCGCTTGA | 51434 |
rs765729638 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397924 | GATCGGGAAAGCCAA[C/T]GGGATAGCAAGAGGA | 51434 |
rs765869196 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378113 | TATTTATTTTTTTTG[C/T]GACAGAGTTTCACTC | 51434 |
rs765955989 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378994 | CTCCCAAGTAGCTGG[C/G]ACTACAGGCGTGCAC | 51434 |
rs765990501 | snp | G/T | 3.2969e-05 | 0.00405998 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388606 | CTTCTTGTACAGGTT[G/T]GCCAGCATCATGTTT | 51434 |
rs766012952 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397545 | GCCTGGCGACAGAGC[A/G]AGATCTCGTCTCAAA | 51434 |
rs766049396 | snp | G/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404607 | GAGACAGTCGTTTTG[G/T]TCTAGATTTTGTTTT | 51434 |
rs766082531 | in-del | -/TTTTCTT | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404823 | ATCATCACTGTGAAC[-/TTTTCTT]TTTTCTTTTTTTCGA | 51434 |
rs766100515 | snp | A/C | 5.04274e-05 | 0.00502107 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382811 | TCTTAATCTACTGAC[A/C]ACTGGGGAGAAAAGA | 51434 |
rs766116039 | snp | G/T | 1.68168e-05 | 0.00289967 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395060 | GAGAGGGAGCAGGGT[G/T]AGGAGAGCTGAGGAG | 51434 |
rs766205420 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389481 | TTAAGGCTTTGGCCC[A/G]TAGGTACTAACTCAC | 51434 |
rs766246442 | snp | A/G | 9.35016e-05 | 0.00683682 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403641 | ATCCTGCTCTGCAAA[A/G]CCGCGGGCAGCGGCG | 51434 |
rs766255835 | in-del | -/AC | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372964 | AACTACTGTACACTT[-/AC]AGTTTTTACATTTTA | 51434 |
rs766327105 | snp | A/C | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386345 | TTATCAGATAAGGAT[A/C]CAACATCTGTGCCTG | 51434 |
rs766408974 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396071 | AGGGTTTGTGTTCCT[A/G]TAAGAATCTAATGCC | 51434 |
rs766427112 | in-del | -/GGGCAGCG | 5.44766e-05 | 0.00521875 | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403646 | GCTCTGCAAAGCCGC[-/GGGCAGCG]GCGGCAGCACTGACT | 51434 |
rs766432476 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397744 | CTACTAAAAATACAA[A/G]ATTAGACGGGTGTGG | 51434 |
rs766536374 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376376 | AGAAATTTTCCATCC[C/T]GGCTAACACAGTGAA | 51434 |
rs766702987 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374205 | TCACTGTCGCTGCCC[C/T]CCAGGTCCCCTTCTT | 51434 |
rs766754223 | snp | C/G | 1.66203e-05 | 0.00288268 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376050 | TGGCCTTCCCCCAAG[C/G]GAGGCTAGTGCCTAC | 51434 |
rs766767310 | snp | C/G/T | 9.02323e-05 | 0.00671625 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403677 | ACTGACTCGAAAAGC[C/G/T]GGTAGAGGATCCTTA | 51434 |
rs766877353 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387556 | TATTTTTACAGGTCT[C/T]CAACAGAGATGATTA | 51434 |
rs766883484 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401665 | GGAGGCCGAGGCGGC[C/G]GGATCACCAGAGGTC | 51434 |
rs766906274 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378860 | ACCTAACTCTAACTA[-/T]TTTTTTTTTTTTTTT | 51434 |
rs766907617 | in-del | -/ACA | 1.6764e-05 | 0.00289512 | cds-indel, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387884 | CTTTTACAGAAAGGG[-/ACA]ACAAGCCTAAACCAA | 51434 |
rs766944853 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373067 | GCTGTGACACCCACC[A/C]CTCACCTCCGATTAA | 51434 |
rs766950438 | snp | C/T | 3.43189e-05 | 0.00414225 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395254 | ATTTCTTTGAAACGT[C/T]ATTCCAACAATATGA | 51434 |
rs767013286 | snp | A/G | 5.03225e-05 | 0.00501585 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395070 | AGGGTTAGGAGAGCT[A/G]AGGAGAAAAACACAT | 51434 |
rs767125699 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380036 | TAACTCTGGCCCAAG[A/G]TAAGATGGCCACGAA | 51434 |
rs767151483 | snp | A/C | 1.65337e-05 | 0.00287517 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377626 | ATAAGACCTGAAAAA[A/C]GTAAAACACGTGAAG | 51434 |
rs767165016 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392196 | TTATTCTTGGAGTAA[C/G]AGAAGACTTTCATAG | 51434 |
rs767294556 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379173 | AGCCAATTACCTAAC[G/T]CTTAAGGGCAACATG | 51434 |
rs767331395 | snp | C/T | 1.7009e-05 | 0.0029162 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381864 | CTTAAGTAGCAGAGC[C/T]TGAACACTATTACTG | 51434 |
rs767395535 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391456 | TTAGACACATTTTGA[C/T]TCACTTCCTTGTCCT | 51434 |
rs767425887 | snp | C/G | 5.33262e-05 | 0.00516336 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374110 | AAGTGCTCAGAGCAG[C/G]GCAGGCCACTGCGGC | 51434 |
rs767500635 | snp | A/C | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375035 | CCACGCCTAGCAAAC[A/C]CCACCTCTAATGGAA | 51434 |
rs767659183 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376091 | TACTATACTGGTCCA[C/T]TGCCTCCTGATACTC | 51434 |
rs767743380 | in-del | -/AAGT | 1.75823e-05 | 0.00296493 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387920 | AAAGCAGAAGAAAGA[-/AAGT]AAGGCACGATATCTC | 51434 |
rs767863216 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398034 | GCAGATCACTGAAGG[C/T]TGGGAGTTTGAGACT | 51434 |
rs767924239 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110376986 | AATAAAAAATAAAAA[A/G]ATTAGCTGGGCATGG | 51434 |
rs767984314 | in-del | -/A | 0.000118744 | 0.0077044 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403766 | CCCCAAGCAAGAGGT[-/A]ACTACTGAAGTGCCC | 51434 |
rs767997930 | snp | C/T | 1.67304e-05 | 0.00289222 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386511 | CCTTTAAATCTATTA[C/T]AAATCCTCTTAGTTG | 51434 |
rs768045854 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382316 | CATTCACCAACTCAG[C/T]TAATGCTTAACCCTA | 51434 |
rs768053095 | snp | A/G | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387828 | GTCCAAGTTAGGCAC[A/G]GTTTGGATCACATTC | 51434 |
rs768116042 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382701 | CAGTCTCCCAAAGTG[C/T]TGAGATTACAGGCAT | 51434 |
rs768163388 | snp | A/G | 1.68849e-05 | 0.00290554 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396425 | ATACACCAAAAGCTG[A/G]TACTTCTGAGGTGGG | 51434 |
rs768190716 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384471 | GCACTTTGGGAGGCC[A/G]AGGTGGAAATTCAAG | 51434 |
rs768233115 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385903 | TTTTCTGTTGTTCAC[A/G]CCTAATTACTGCCTT | 51434 |
rs768287933 | snp | C/T | 8.76693e-05 | 0.00662019 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403506 | CTCCTCAGCCCCAGG[C/T]AGCTACCCGCCTCAA | 51434 |
rs768346328 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381970 | AAAAAAAAAAAAAAA[A/C]AAACACAAAAACCCC | 51434 |
rs768371441 | in-del | -/CT | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401767 | AGGCGGGCGGATCAC[-/CT]GAGGTCAGGAGATCG | 51434 |
rs768390954 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383686 | AGGAGTTCGAGACTA[A/G]GCTAACAGGTGAAAC | 51434 |
rs768394350 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395882 | TATCATCTAAATCAG[C/T]GGTCCCCAACCTTTT | 51434 |
rs768490213 | in-del | -/CA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392092 | CAAGACTCCACCTCA[-/CA]AAAAAAAAAAAAAAA | 51434 |
rs768499967 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389236 | AACTGGAATAACATT[C/T]ATTTAAGAAATGGTA | 51434 |
rs768547668 | in-del | -/T | 0.000116456 | 0.00762984 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382971 | ATTCCTAGAAGAGAA[-/T]GGACATAGTGAGAAG | 51434 |
rs768592404 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387790 | TGCACAAAAGCATAC[A/G]CTTTGATCCACACAG | 51434 |
rs768637059 | snp | C/G | 1.64933e-05 | 0.00287165 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395166 | CTTTATCTTGTTTTA[C/G]CATTGTATAACATTC | 51434 |
rs768645921 | snp | C/T | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375834 | TGAACACAGATGTTA[C/T]AGTGGTGTGGGATGG | 51434 |
rs768735830 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374667 | AACAAACATTACCAG[A/G]TAAATTCAAATGGAA | 51434 |
rs768758481 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377517 | AACGGTGGCTAAAAG[A/G]GTAAGGGTCTGTGCA | 51434 |
rs768772375 | snp | C/G | 3.30071e-05 | 0.00406232 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376213 | TCATATTTCTGTTCT[C/G]TGCCTGGGGGAATAA | 51434 |
rs768776206 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400564 | GTTTCAAACTATCCT[A/G]TAACATCTTTAAGAA | 51434 |
rs768797447 | snp | A/T | 3.64392e-05 | 0.00426828 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377670 | TTACCATTCCAACCC[A/T]TGCTTCCACTCTGAC | 51434 |
rs768849261 | snp | C/T | | | intron-variant, missense, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401481 | TCAGAGAAGGCTCTT[C/T]AGGAGAGATATCCAG | 51434 |
rs768882166 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379825 | AGATCTATTTTAATG[C/T]CTGTGACTGAGTCAC | 51434 |
rs768900503 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403942 | CTACTCGGTCAATTT[C/G]AATGAGTCTGAGAGG | 51434 |
rs769056153 | in-del | -/TTTAT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393393 | GCCATTCTTTATTCC[-/TTTAT]TTTATTAATAAACTC | 51434 |
rs769131120 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378770 | CAGATTTTCTCTGCA[C/T]ACTCCTCCACCCTAG | 51434 |
rs769259837 | snp | A/C | 3.45913e-05 | 0.00415866 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388674 | GTATATTGCAAAGAA[A/C]ATCTCTCACCATGAA | 51434 |
rs769291661 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391811 | AATTAAAATGGCTTC[C/T]TGGCCGGGCGTGGTG | 51434 |
rs769378462 | snp | A/C/G | 0.00021663 | 0.0104055 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403646 | GCTCTGCAAAGCCGC[A/C/G]GGCAGCGGCGGCAGC | 51434 |
rs769381704 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405581 | TTCAGGGCTGCTTCA[A/G]GTGGGATTGGGGGTG | 51434 |
rs769422236 | in-del | -/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404306 | CTTAACGTTTTAGGA[-/T]AAGTTTTACACAAGT | 51434 |
rs769453795 | in-del | -/A | 5.32297e-05 | 0.00515868 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374114 | CTCAGAGCAGGGCAG[-/A]GCCACTGCGGCCATG | 51434 |
rs769561629 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377470 | TCTAATAATGTTTTG[A/G]CTTTCTCCTGTGTCA | 51434 |
rs769607628 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398377 | GCCAAGATCATGCCA[C/T]TTGTACACCAGCCTG | 51434 |
rs769651432 | snp | A/G | | | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377718 | ACCTTCAAAGTTTCA[A/G]ACAAAGGGCAGGCCA | 51434 |
rs769662800 | snp | A/G | 1.65685e-05 | 0.00287819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376232 | CTGGGGGAATAAAAA[A/G]GACCCTCACTTAAGT | 51434 |
rs769741989 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390407 | CACAACAGTATTTGC[C/T]AGATCATTAACCTAA | 51434 |
rs769752251 | in-del | -/GA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387215 | TGCACTCTAGCCTGG[-/GA]GAGAGAGAGAGAGAG | 51434 |
rs769773172 | snp | A/C | 6.30219e-05 | 0.00561311 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403573 | TGCTGAGGAGCCGCA[A/C]GTTGGAGTGCAGCCC | 51434 |
rs769894816 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376138 | AAATCTCCTAGGATC[C/T]GATGCAGGACACAGT | 51434 |
rs769907413 | snp | A/G | 6.57268e-05 | 0.00573228 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403744 | TCGGGTCCACACGCG[A/G]CACCACCCCCAAGCA | 51434 |
rs769915811 | in-del | -/ACTC | 1.65021e-05 | 0.00287241 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396362 | AGCCATGGTATACTT[-/ACTC]ACAGCATTCCGATAT | 51434 |
rs770094008 | snp | A/G | | | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401530 | AGGCAACGCTGAGAT[A/G]AGGACCGTCGCAGGA | 51434 |
rs770251791 | snp | A/C | 0.00066641 | 0.0182417 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396247 | AAAAAAAAAAAATCA[A/C]AATTCTATCTCCAAT | 51434 |
rs770280648 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401686 | ACCAGAGGTCAGGAG[C/T]TGAAGACCAGACTGG | 51434 |
rs770300870 | in-del | -/AA | 1.65641e-05 | 0.00287781 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377627 | AAGACCTGAAAAAAG[-/AA]TAAAACACGTGAAGA | 51434 |
rs770361211 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380799 | CTCTACTAAAAATAC[A/C]AAAAATTAGCCAGGT | 51434 |
rs770381068 | snp | A/G | 1.95835e-05 | 0.00312911 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377687 | GCTTCCACTCTGACA[A/G]CTCTCCAAATTGCTA | 51434 |
rs770448842 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379926 | ATAACAAAACAAAGT[G/T]GGACCCTGATTGTGC | 51434 |
rs770459872 | snp | A/G | 1.78341e-05 | 0.00298609 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374095 | TCCTTCAGTCCACGG[A/G]AGTGCTCAGAGCAGG | 51434 |
rs770507662 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386431 | AAGCTTCCCAATAGG[C/T]CCACGTTATCTCGCA | 51434 |
rs770516781 | snp | A/G | 3.56812e-05 | 0.00422366 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374093 | GTTCCTTCAGTCCAC[A/G]GAAGTGCTCAGAGCA | 51434 |
rs770541076 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394587 | TGAGCCCCCATGCTA[C/T]TGCACTCCAGCCTGG | 51434 |
rs770604729 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372752 | GGCTGGTCTCAAACT[C/T]CTGGCCTCAAGTGAT | 51434 |
rs770701456 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385106 | CCCGTCTCTTCTAAA[A/T]AAATACAAAAATTAG | 51434 |
rs770740746 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386123 | GGAGAAGACACTTGA[A/G]TTCAAGCAAAAACAG | 51434 |
rs770747404 | snp | C/T | 8.57861e-05 | 0.00654872 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395251 | AATATTTCTTTGAAA[C/T]GTTATTCCAACAATA | 51434 |
rs770775189 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398675 | AAAGCTACAGCAGGC[C/T]GGGGCATGGTGGCTC | 51434 |
rs770814512 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400040 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 51434 |
rs770824248 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386300 | CCCAACAACAGCCAC[C/T]GTCTTCCTGCCCCAA | 51434 |
rs770939172 | snp | A/C | 2.02034e-05 | 0.00317826 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403699 | GGATCCTTAGGGAAG[A/C]CTCCAAAATGGCGGC | 51434 |
rs771053134 | snp | C/G | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387803 | ACGCTTTGATCCACA[C/G]AGAGAGCCAGTCCAA | 51434 |
rs771079899 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382322 | CCAACTCAGTTAATG[C/T]TTAACCCTAGAAGGA | 51434 |
rs771088599 | snp | C/G | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377068 | CTTGAACCCGGGAGG[C/G]GGAGGTTGCAGTGAG | 51434 |
rs771120525 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396580 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 51434 |
rs771168913 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390872 | GTCACTTTAAAAGAA[C/T]GAGTTTTGAGTAATA | 51434 |
rs771233453 | snp | C/G | 1.65228e-05 | 0.00287422 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388494 | CATGCCATGAAAACA[C/G]GCAGGAAATATCTCT | 51434 |
rs771257033 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389591 | TGTAACTTTGTAAAG[A/C]TAAATTAAAATAATC | 51434 |
rs771444645 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396276 | ATTACCTGACTTTGT[A/G]GAGTAGATGCAGAAT | 51434 |
rs771449357 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380830 | GTAATCCTAGCTACT[A/G]GGGAGGCTGAGGCAG | 51434 |
rs771499699 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381832 | TGGACTCTGCCCATG[C/T]TCCTAAGTGCTGCTC | 51434 |
rs771567026 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395597 | CCTGGCCTCATCTTC[-/T]TTTTTTTTTTTTTGA | 51434 |
rs771626202 | snp | A/G | 5.92014e-05 | 0.00544033 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381961 | CAGCTGGAGAAAAAA[A/G]AAAAAAAAAAAACAC | 51434 |
rs771640300 | snp | G/T | 1.75984e-05 | 0.00296629 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374371 | AGAGGCCTGAATCTC[G/T]GCCTTGCTCTTGCTG | 51434 |
rs771659945 | snp | C/G | 3.31945e-05 | 0.00407383 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396399 | TTATCATGAAAGAGA[C/G]AATCTGCATGATACA | 51434 |
rs771740342 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396295 | TAGATGCAGAATTTC[C/T]AGTTGAAGGTCTCAC | 51434 |
rs771757058 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393867 | GCGAAACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs771800898 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379053 | TTTTAGTAGAGATGG[C/T]AGTTCACCATGTTGG | 51434 |
rs771827539 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373082 | CCTCACCTCCGATTA[A/C]TTGTATACTCAGAGC | 51434 |
rs771873408 | snp | C/G | 3.40397e-05 | 0.00412537 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374345 | CAAACTAGGGGACAA[C/G]AAAACAAAGGAGAGG | 51434 |
rs771964665 | snp | G/T | 1.66225e-05 | 0.00288287 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374166 | ATGCCGAACCACTGC[G/T]CCTGGTCAGCCCACT | 51434 |
rs772020710 | snp | A/G | 0.000112975 | 0.00751497 | missense, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403722 | ATGGCGGCGTCGCCG[A/G]GGTCCATCGGGTCCA | 51434 |
rs772055770 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388039 | AAACCATAATTTAGT[A/G]TTTCTTTTCTTTTTG | 51434 |
rs772059942 | in-del | -/A/GA | 0.000702001 | 0.0187218 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381952 | AGCTGTGACAGCTGG[-/A/GA]AGAAAAAAAAAAAAA | 51434 |
rs772072113 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386463 | TAAGGATTTTTTCTC[C/T]AGTGAACTTTAAGAT | 51434 |
rs772119984 | snp | A/G | 1.67203e-05 | 0.00289134 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376255 | ACTTAAGTCATGTAC[A/G]AAAAAACCACAACTA | 51434 |
rs772139448 | in-del | -/T | 1.6865e-05 | 0.00290383 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382796 | AGAGCAACCATTATC[-/T]CTTAATCTACTGACA | 51434 |
rs772143395 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401284 | ACCAGGTCCAGGCAT[C/T]GTACTCCTCCATTTA | 51434 |
rs772180548 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387767 | TTGCTCTTGAGTTGT[A/C]ACCAGTGTGCACAAA | 51434 |
rs772233373 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400273 | GTCTACTTACACATG[A/C]ATTAAGTTATCTCTG | 51434 |
rs772281431 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384020 | AGCCTGGCCAAGATG[A/G]TGAAACCCCGTCTCT | 51434 |
rs772304167 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391736 | ATATCCACAGGTCAT[A/T]ATGAAGGAGATTATG | 51434 |
rs772387908 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405517 | GTCGTAAAGTGTTGC[A/G]GCAGCGAAAATTTTT | 51434 |
rs772390778 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378044 | TCTCCAGCTGCATTC[A/G]GTCACCTGTAGGGCT | 51434 |
rs772400319 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377500 | ACTGGGTCTTCAAGA[A/C]AAACGGTGGCTAAAA | 51434 |
rs772402967 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399865 | CTTTGGGAGGCCAAG[A/G]AGGGAGGATCACCTG | 51434 |
rs772541248 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390934 | CAGTGGTTCACACCT[C/T]TAATCCTAGCACTTT | 51434 |
rs772607400 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397283 | AGAAAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 51434 |
rs772651489 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404232 | CCCTAGATCCGTGGA[A/G]ATAAAGGCTGGATCC | 51434 |
rs772651852 | snp | G/T | 1.66568e-05 | 0.00288585 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382973 | TTCCTAGAAGAGAAG[G/T]ACATAGTGAGAAGAG | 51434 |
rs772836382 | snp | A/G | 1.66164e-05 | 0.00288235 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376240 | ATAAAAAAGACCCTC[A/G]CTTAAGTCATGTACA | 51434 |
rs772869804 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391209 | AAACAAACAAAAAAA[C/G]TCAACTATTTTAAAA | 51434 |
rs772935157 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384980 | TAAAGATCACTGCCT[C/T]GGGCTGGGTGCAGTG | 51434 |
rs773020694 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379266 | CTACTGGAACTTCAG[-/A]AAAAAAACAGAATGC | 51434 |
rs773023079 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382981 | AGAGAAGGACATAGT[A/G]AGAAGAGGTGTTTTA | 51434 |
rs773169754 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397447 | AGTCCCAGCTACTCG[A/G]GAAGCTGAGGCAGGA | 51434 |
rs773175187 | in-del | -/TTAC | 3.29478e-05 | 0.00405867 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386319 | TTCCTGCCCCAAGAA[-/TTAC]TTACCTTTTATCAGA | 51434 |
rs773205851 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376330 | TGCAACACAAAGCGA[A/G]GGCAAGCACACCTGA | 51434 |
rs773293057 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381823 | ATTGCTTCTTGGACT[C/T]TGCCCATGTTCCTAA | 51434 |
rs773294463 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389433 | TTTTCTTTGACAATT[C/T]GACTTGTGGCTAGAC | 51434 |
rs773433289 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386026 | CCATCCAAATTCTCA[C/G]TCAGGCACACCATAA | 51434 |
rs773448071 | in-del | -/A | 1.96903e-05 | 0.00313763 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396461 | AACTCACTAGAAAAC[-/A]AAGAGAAAATGTAAT | 51434 |
rs773472548 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374798 | CATTTCAGGAGCCAA[C/T]CAAAAACATCACGCT | 51434 |
rs773505960 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403033 | AGGCGTGAGCCACCG[A/C]GCCCGGCCCCGTTTT | 51434 |
rs773596521 | snp | A/C | 1.66302e-05 | 0.00288355 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386496 | TTATTAAACATTGAA[A/C]CTTTAAATCTATTAT | 51434 |
rs773597810 | snp | C/T | | | intron-variant, synonymous-codon, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401539 | TGAGATGAGGACCGT[C/T]GCAGGAGGAACAGCA | 51434 |
rs773688790 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386436 | TCCCAATAGGTCCAC[A/G]TTATCTCGCAATAAG | 51434 |
rs773742168 | snp | C/T | 3.35841e-05 | 0.00409767 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374155 | CCCCTCACTGCATGC[C/T]GAACCACTGCTCCTG | 51434 |
rs773768233 | snp | A/G | 1.69703e-05 | 0.00291288 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395237 | TAAAAGACAATGGAA[A/G]TATTTCTTTGAAACG | 51434 |
rs773802195 | snp | G/T | 3.56754e-05 | 0.00422332 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374098 | TTCAGTCCACGGAAG[G/T]GCTCAGAGCAGGGCA | 51434 |
rs773853846 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380813 | CAAAAAATTAGCCAG[A/G]TGTAATCCTAGCTAC | 51434 |
rs773932388 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394612 | GCCTGGGCAACTTTG[C/T]AGTGAGCCCCCATGC | 51434 |
rs773943892 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379938 | AGTTGGACCCTGATT[A/G]TGCCCACTCTGGAGG | 51434 |
rs773971089 | snp | A/C | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372816 | ACAGGTGTGAGCACG[A/C]CTAGCCTTATATGTC | 51434 |
rs774058530 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386141 | CAAGCAAAAACAGCT[A/G]CTCAAATGGTATTAC | 51434 |
rs774114886 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392022 | GCTTGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 51434 |
rs774132905 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398589 | CCTAATGAGGAACTC[A/G]TATTTTCAACCTCCA | 51434 |
rs774182769 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377673 | CCATTCCAACCCATG[A/C]TTCCACTCTGACAGC | 51434 |
rs774196567 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383711 | TGAAACCCCATCTCT[A/G]CTAAAAATACAAAAA | 51434 |
rs774268194 | snp | A/G | 6.31253e-05 | 0.00561771 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403653 | AAAGCCGCGGGCAGC[A/G]GCGGCAGCACTGACT | 51434 |
rs774315287 | snp | C/T | 0.000115334 | 0.00759299 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386306 | AACAGCCACTGTCTT[C/T]CTGCCCCAAGAATTA | 51434 |
rs774539300 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377881 | AGCACATGTAAGGAA[C/G]CTGCAGCATGTGAGC | 51434 |
rs774600740 | snp | A/T | 6.62394e-05 | 0.00575459 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376059 | CCCAAGGGAGGCTAG[A/T]GCCTACCTTAGTGCT | 51434 |
rs774602007 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397847 | TTGCTGTGAGCCGAG[A/G]TTGCGCCACTACACT | 51434 |
rs774645270 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390908 | TGAAAAAGTCAATTA[C/T]TGGCCGGGCGCAGTG | 51434 |
rs774685307 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403184 | AAAAAAACGTTCTTC[C/T]GGAAGGAGCCGAGAG | 51434 |
rs774733081 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389610 | ATTAAAATAATCCTA[C/T]CTAACATGCAACTGG | 51434 |
rs774800150 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396279 | ACCTGACTTTGTGGA[A/G]TAGATGCAGAATTTC | 51434 |
rs774811866 | snp | C/G | 3.55935e-05 | 0.00421847 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374374 | GGCCTGAATCTCTGC[C/G]TTGCTCTTGCTGGCT | 51434 |
rs774880509 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403655 | AGCCGCGGGCAGCGG[-/C]GGCAGCACTGACTCG | 51434 |
rs774922917 | snp | C/T | 1.68224e-05 | 0.00290016 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381855 | TGCTGCTCCCTTAAG[C/T]AGCAGAGCTTGAACA | 51434 |
rs774995922 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380058 | GGCCACGAAAAAGAA[C/T]AGGCCTAACAGGCCA | 51434 |
rs775085875 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394921 | GTAGTATTCTCCAGC[C/T]ATCATTTTCATCAGC | 51434 |
rs775145723 | snp | C/G/T | 5.46543e-05 | 0.00522725 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381716 | CTGCTGCCACACCCA[C/G/T]GGATTCACACCATTC | 51434 |
rs775181443 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395825 | TTACAGGCGTGAGCC[A/G]CTGCGCCCAGCTTCT | 51434 |
rs775181644 | snp | A/G | 1.66457e-05 | 0.00288489 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396409 | AGAGAGAATCTGCAT[A/G]ATACACCAAAAGCTG | 51434 |
rs775237541 | in-del | -/CT | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403795 | CCGAATAAAAAGAAA[-/CT]CGAGTCCCTGCTCCT | 51434 |
rs775354583 | snp | A/T | 0.000113154 | 0.00752092 | missense, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403725 | GCGGCGTCGCCGGGG[A/T]CCATCGGGTCCACAC | 51434 |
rs775492366 | snp | A/C | 1.648e-05 | 0.0028705 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388530 | GAATGGCATCAAGGG[A/C]TAATGGGCACTGCCT | 51434 |
rs775495920 | snp | G/T | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386466 | GGATTTTTTCTCTAG[G/T]GAACTTTAAGATATT | 51434 |
rs775528352 | in-del | -/A | 1.67674e-05 | 0.00289541 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382821 | CTGACAACTGGGGAG[-/A]AAAGAGAATGCATAA | 51434 |
rs775552816 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388040 | AACCATAATTTAGTA[C/T]TTCTTTTCTTTTTGA | 51434 |
rs775617033 | snp | A/C | 1.67312e-05 | 0.00289229 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376260 | AGTCATGTACAAAAA[A/C]ACCACAACTACCATT | 51434 |
rs775654101 | in-del | -/GTTT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387145 | CTGAGCAGGAGGATG[-/GTTT]GAGCCCGGGAGATTG | 51434 |
rs775730668 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385347 | AAAAGGGACCTATGC[C/T]CACTGTTACCCATCT | 51434 |
rs775747178 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400306 | ATGACACACGAAAAA[A/G]TAGTTATTGCCTCTG | 51434 |
rs775836296 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390974 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 51434 |
rs775836962 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398887 | GAGGCAGAGGTTGCG[A/G]TGAGCCAAGATAGTG | 51434 |
rs775854160 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374409 | CGTCATCTCCCTGGC[C/T]CGGCAGTGAAATGAC | 51434 |
rs775860007 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378062 | CACCTGTAGGGCTAG[A/G]TTTAAGATGGAAGAC | 51434 |
rs775879078 | snp | A/C | 0.000104221 | 0.00721801 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381966 | GGAGAAAAAAAAAAA[A/C]AAAAAAACACAAAAA | 51434 |
rs775922227 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404272 | CTGATACCCATATAA[A/G]CCAGTATGTGTCTGG | 51434 |
rs775948214 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391740 | CCACAGGTCATTATG[A/T]AGGAGATTATGGTAT | 51434 |
rs776059081 | snp | A/C | 0.000272898 | 0.0116779 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381971 | AAAAAAAAAAAAAAA[A/C]AACACAAAAACCCCA | 51434 |
rs776192421 | snp | G/T | 9.85513e-05 | 0.00701897 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403531 | CCTCAACTCACGGGT[G/T]GTTATTACTCATTGT | 51434 |
rs776203843 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379568 | GGATCAAGAAGTTAA[A/T]CTGAAATCAATGGTT | 51434 |
rs776229522 | snp | G/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387793 | ACAAAAGCATACGCT[G/T]TGATCCACACAGAGA | 51434 |
rs776312502 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382930 | TCTAGCCGCCCTTCT[C/T]GTGCCAGTAGGTAGC | 51434 |
rs776444558 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395886 | ATCTAAATCAGCGGT[C/T]CCCAACCTTTTTGGC | 51434 |
rs776485115 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381587 | TGATCTGCCCGTCTC[A/G]GCCTCCCAAAGTGCT | 51434 |
rs776508303 | snp | A/G | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374187 | TCAGCCCACTGGGCC[A/G]CCTCACTGTCGCTGC | 51434 |
rs776561997 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391651 | AGAATGATGGCAATG[-/A]AAATCAAGCAGTGGA | 51434 |
rs776687633 | snp | G/T | | | intron-variant, missense, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401492 | TCTTTAGGAGAGATA[G/T]CCAGGCTAAAACCTG | 51434 |
rs776706760 | snp | A/G | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375858 | GGGATGGTTATGAGT[A/G]AAACAGTTCTCTAAT | 51434 |
rs776792536 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374731 | TACAAAAAATAGGAA[C/T]TTCTCTGAGTATAGG | 51434 |
rs776889608 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386722 | CAGAACACAACATAC[A/G]CTACATGGTGTTAAA | 51434 |
rs776949011 | in-del | -/GAGAA | 1.66879e-05 | 0.00288855 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382981 | AGAGAAGGACATAGT[-/GAGAA]GAGGTGTTTTAAGAA | 51434 |
rs777012063 | snp | A/G | 0.000210342 | 0.0102531 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403659 | GCGGGCAGCGGCGGC[A/G]GCACTGACTCGAAAA | 51434 |
rs777031732 | snp | C/G | 1.6832e-05 | 0.00290099 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395051 | AAACATGGAGAGAGG[C/G]AGCAGGGTTAGGAGA | 51434 |
rs777094203 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379894 | CAGGGTCAATTCACA[C/T]GAACTTAAAATATTA | 51434 |
rs777201239 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387930 | AAAGAAAGTAAGGCA[C/T]GATATCTCTCTTCCA | 51434 |
rs777229395 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373858 | TAGAAATTAGTTATA[C/T]AAAAAGTACTCTTGG | 51434 |
rs777275120 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401139 | CTTAAAGGACTTTTC[C/T]CTTCTGACCTAGACC | 51434 |
rs777343991 | in-del | -/A | 0.000100514 | 0.00708851 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376254 | ACTTAAGTCATGTAC[-/A]AAAAAAACCACAACT | 51434 |
rs777382780 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386427 | TGCCAAGCTTCCCAA[C/T]AGGTCCACGTTATCT | 51434 |
rs777399112 | snp | A/G | 1.95131e-05 | 0.00312349 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403694 | GTAGAGGATCCTTAG[A/G]GAAGACTCCAAAATG | 51434 |
rs777534363 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388623 | CCAGCATCATGTTTA[C/T]CTGTACAAACACAAA | 51434 |
rs777556847 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400022 | CTTGAACCCAGCAGG[C/T]GGAGGTTGCAGTGAG | 51434 |
rs777618067 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401321 | GTGTGAACTTGGACA[A/G]GGGTATTTCACCTCC | 51434 |
rs777660692 | in-del | -/TC | 0.000357328 | 0.0133618 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395242 | GACAATGGAAATATT[-/TC]TTTGAAACGTTATTC | 51434 |
rs777669420 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379351 | GTAAGAAATATCAAA[A/G]GGTGTAGTCAGAGTT | 51434 |
rs777720148 | snp | A/G | 0.00282317 | 0.0374648 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381959 | GACAGCTGGAGAAAA[A/G]AAAAAAAAAAAAAAC | 51434 |
rs777720590 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391277 | ACCAGTTATAAACAC[-/A]AAGCAGTCATCATTT | 51434 |
rs777787036 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391481 | TGTCCTTTACATAGA[C/T]TGAGAAGCCAGTTAA | 51434 |
rs777877097 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405237 | TCCGCGTGAGAGAGT[C/T]GTGATCGATTGAGTA | 51434 |
rs777960162 | snp | C/T | 1.65436e-05 | 0.00287602 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396387 | TTCCGATATTCCTTA[C/T]CATGAAAGAGAGAAT | 51434 |
rs777965099 | snp | C/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404167 | AGTCAGGCTTCGGCC[C/G]TGGGGGAACTCCTTG | 51434 |
rs778044685 | snp | A/G | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382858 | CCAGAAACCACCCAC[A/G]GTTCTGCATGCTGAT | 51434 |
rs778072322 | snp | A/T | 1.67953e-05 | 0.00289782 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387699 | ACTTCCAGACAAGCA[A/T]AGGGCCTCAAGAACA | 51434 |
rs778072382 | snp | C/T | 1.72653e-05 | 0.00293809 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374139 | GCCATGGAGCTGCCG[C/T]CCCCTCACTGCATGC | 51434 |
rs778283085 | in-del | -/AC | 7.299e-05 | 0.00604067 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381972 | AAAAAAAAAAAAAAA[-/AC]ACACAAAAACCCCAG | 51434 |
rs778326396 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396406 | GAAAGAGAGAATCTG[A/C]ATGATACACCAAAAG | 51434 |
rs778392635 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396263 | AATTCTATCTCCAAT[C/T]ACCTGACTTTGTGGA | 51434 |
rs778465893 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376888 | ACCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 51434 |
rs778494172 | snp | C/T | 3.30797e-05 | 0.00406679 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387743 | GTGGCTCTCACCAGA[C/T]GGTACTGATTGCTCT | 51434 |
rs778512682 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385904 | TTTCTGTTGTTCACG[C/T]CTAATTACTGCCTTT | 51434 |
rs778571694 | in-del | -/AAT | 1.73312e-05 | 0.00294369 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395263 | AAACGTTATTCCAAC[-/AAT]ATGACAGTTCTTCAA | 51434 |
rs778617063 | snp | A/G | 1.72107e-05 | 0.00293343 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374354 | GGACAACAAAACAAA[A/G]GAGAGGCCTGAATCT | 51434 |
rs778626201 | snp | A/C | 1.79351e-05 | 0.00299454 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396223 | ATTCTTGGAGTCTTT[A/C]TCAAAAAAAAAAAAA | 51434 |
rs778642374 | snp | C/T | 5.22653e-05 | 0.00511174 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377652 | TGAAGACATTCAATG[C/T]CATTACCATTCCAAC | 51434 |
rs778681300 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381769 | TCATAACAATCTAAG[C/T]GACAAGGTGCGAGCC | 51434 |
rs778746037 | in-del | -/AAAAAAAAAAAA | | | | | GRCh38.p7 | 12:110389082 | GTGAGACTCCATCTT[-/AAAAAAAAAAAA]AAAAAAAAAGAAAAG | 51434 |
rs778877038 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401208 | GTAAAAGTTTCCATT[A/G]TAACGCCATTTGGAG | 51434 |
rs778912289 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379394 | ATCTCCAAATGGCAG[C/G]TTAAGAAGCCTCACT | 51434 |
rs778969082 | snp | C/T | 2.4145e-05 | 0.00347446 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403711 | AAGACTCCAAAATGG[C/T]GGCGTCGCCGGGGTC | 51434 |
rs779000200 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378526 | GCTGAGGGCTTCCCT[A/G]AACGAGATGAACAGT | 51434 |
rs779016457 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392873 | CCACGTCGGCTCACC[A/G]CAACCTCTGCCTCCT | 51434 |
rs779024506 | in-del | -/TAT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400211 | GCTTAGATACAAAAG[-/TAT]TATTACATCCACAGA | 51434 |
rs779077818 | in-del | -/ATA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396009 | GGCATTAGTCAGATT[-/ATA]ATAAGGAACACACAA | 51434 |
rs779092483 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405442 | GTACACATGCAGGCT[C/T]GGGTTCAGAGGCCTG | 51434 |
rs779099539 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382891 | GAGATATTGAAAAGG[C/T]GGCATCCAAGGTTCT | 51434 |
rs779106498 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391702 | TTAACATTACTATTT[C/T]CAAAAAAAAGTCCTA | 51434 |
rs779142936 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394669 | GTGAAATTCCACCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs779280065 | in-del | -/AAGTAAAACACGTG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377625 | GATAAGACCTGAAAA[-/AAGTAAAACACGTG]AAGACATTCAATGCC | 51434 |
rs779442465 | snp | A/G | 2.91958e-05 | 0.00382061 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396497 | TTTTCCTCCCTTTCA[A/G]TCCAAGCTCCCCCAG | 51434 |
rs779476741 | snp | A/G | 1.65726e-05 | 0.00287855 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396395 | TTCCTTATCATGAAA[A/G]AGAGAATCTGCATGA | 51434 |
rs779542207 | snp | A/G | 0.000191596 | 0.00978577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381962 | AGCTGGAGAAAAAAA[A/G]AAAAAAAAAAACACA | 51434 |
rs779559503 | snp | G/T | 9.88582e-05 | 0.00702989 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377411 | GTAGTTCTGCTTTTT[G/T]CACCACAGCCTTAAT | 51434 |
rs779616373 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376180 | GCCAGTGCGTTCCTC[A/G]GCAAAGCAATTCCAT | 51434 |
rs779664549 | in-del | -/TA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401325 | GAACTTGGACAAGGG[-/TA]TTTCACCTCCCTGAG | 51434 |
rs779752908 | in-del | -/AAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389093 | CTTAAAAAAAAAAAA[-/AAAA]AAAAAAAAAGAAAAG | 51434 |
rs779892068 | in-del | -/GACC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387431 | AGAGAGAGAGAGAGA[-/GACC]GACCTTGTCTCAAAA | 51434 |
rs779945494 | snp | A/G | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375471 | AAAGAAACCACTTCT[A/G]TATTAAACAGTAAGA | 51434 |
rs780033421 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389209 | TCTGAACAAAAGACG[C/T]TGCCCTCTGGAAACT | 51434 |
rs780126405 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381047 | CTGGATGGGGGCGAG[C/T]GGTGGGAGGACAAAA | 51434 |
rs780135466 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379777 | ATTTTTAAATGCTTA[C/T]AAAAATATGTTTTGG | 51434 |
rs780178618 | in-del | -/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378990 | CAGCCTCCCAAGTAG[-/C]TGGGACTACAGGCGT | 51434 |
rs780187306 | in-del | -/A/AA/AAA | 0.547474 | 0.10796 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396225 | CTTGGAGTCTTTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 51434 |
rs780227737 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401300 | GTACTCCTCCATTTA[C/T]TGGATGTGTGAACTT | 51434 |
rs780237576 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395141 | ATCCCATCAAGTATA[A/G]CAATGGCATCTTTAT | 51434 |
rs780291180 | snp | A/G | 1.75262e-05 | 0.0029602 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374129 | GGCCACTGCGGCCAT[A/G]GAGCTGCCGCCCCCT | 51434 |
rs780341014 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373757 | CATCCAACTTGGGAG[A/G]TGACATTATCGTGCT | 51434 |
rs780584692 | snp | C/T | 3.29625e-05 | 0.00405958 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386283 | TATTATCTCTGATCC[C/T]CCCCAACAACAGCCA | 51434 |
rs780632272 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385806 | TATTCCTGAGAACTC[A/G]CTGCCAGTGTCCTAA | 51434 |
rs780677540 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405558 | TGGAGAGATAATGGG[C/T]GATGTTTTTCAGGGC | 51434 |
rs780720069 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384572 | ACACCTGTAATCCCA[A/G]CTACTCAAGAGGCTG | 51434 |
rs780728439 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399920 | CCAACATGTTGAAAC[C/G]TCGTCTCTACTAAAA | 51434 |
rs780742694 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374602 | ATACCTATTACCCCT[-/A]AGCATTCTGCTAGAG | 51434 |
rs780818226 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398346 | GCTTGAGCCCAGGAG[A/C]CAGAAGTTGCAGTGG | 51434 |
rs780865314 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392677 | GAAAAAATACTATTC[C/T]TCTCATTTTATAAAT | 51434 |
rs780970303 | snp | A/G | 1.65282e-05 | 0.00287469 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388628 | ATCATGTTTATCTGT[A/G]CAAACACAAATAACA | 51434 |
rs781184953 | snp | C/T | 3.69201e-05 | 0.00429636 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377674 | CATTCCAACCCATGC[C/T]TCCACTCTGACAGCT | 51434 |
rs781275985 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389282 | CTTGATTCTTTCTTG[A/G]TCTTAAAACAGAAGA | 51434 |
rs781355019 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402805 | CAATGATGCGATCAC[A/G]GCTCACTGCAGCCTC | 51434 |
rs781367378 | snp | A/G | 9.92277e-05 | 0.00704301 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381780 | TAAGCGACAAGGTGC[A/G]AGCCGTATGGCCTCC | 51434 |
rs781486148 | snp | C/T | 3.2963e-05 | 0.00405961 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386285 | TTATCTCTGATCCCC[C/T]CCAACAACAGCCACT | 51434 |
rs781496556 | snp | A/G | 9.24599e-05 | 0.00679863 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403679 | TGACTCGAAAAGCCG[A/G]TAGAGGATCCTTAGG | 51434 |
rs781527041 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389914 | TCCAGACTGGGAGAC[A/G]GAGCGAGACTCCGTC | 51434 |
rs781541340 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386404 | TCTCCAGCTCTGAAG[G/T]ACAGATCTGCCAAGC | 51434 |
rs781653356 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396108 | GATCTGACAGGAGGC[A/G]GAGCTCAGGCAGTAA | 51434 |
rs781723057 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395543 | AGTCCTCCTACCTCC[A/G]CCTCTGGAAGTGCTT | 51434 |
rs796192574 | in-del | -/TGAGCAGAGATTGTGCCAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385208 | AGGCGGAGGTTGCAG[-/TGAGCAGAGATTGTGCCAC]TGAGCAGAGATTGTG | 51434 |
rs796290045 | in-del | -/AG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387353 | GAGAGAGAGAGAGAC[-/AG]AGAGAGAGAGAGACA | 51434 |
rs796343629 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383735 | ACAAAAATTAGCTGG[C/G]CATGGTGGCGTGTGC | 51434 |
rs796381988 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383910 | AAAAGAAAAAAAAAA[A/G]AAAAAAGAAGGGCCA | 51434 |
rs796463112 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387294 | GAGAGAGACAGAGAG[A/G]GAGAGAGAGAGAGAG | 51434 |
rs796510186 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387347 | AGAGGCAGAGAGAGA[C/G]AGAGACAGAGAGAGA | 51434 |
rs796517905 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387387 | AGAGAGAGAGACAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs796569385 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387322 | GAGACAGAGAGACAG[A/G]GAGAGAGAGAGAGGC | 51434 |
rs796595026 | in-del | -/AA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | CTGTGACAGCTGGAG[-/AA]AAAAAAAAAAAAAAA | 51434 |
rs796653545 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387394 | GAGACAGAGAGAGAG[A/G]GAGAGAGAGAGAGAG | 51434 |
rs796724726 | snp | A/C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387285 | AGAGAGAGAGAGAGA[A/C/G]ACAGAGAGAGAGAGA | 51434 |
rs796776917 | in-del | -/GA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381952 | AAGCTGTGACAGCTG[-/GA]GAAAAAAAAAAAAAA | 51434 |
rs796794011 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387381 | ACAGAGAGAGAGAGA[A/G]ACAGAGAGAGAGAGA | 51434 |
rs796836183 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387292 | GAGAGAGAGACAGAG[A/G]GAGAGAGAGAGAGAG | 51434 |
rs796883338 | in-del | -/AGAGGC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387332 | GACAGAGAGAGAGAG[-/AGAGGC]AGAGAGAGAGAGAGA | 51434 |
rs796985237 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385986 | AAACAAAATTCCCTA[A/G]AAGGATATTATGGTT | 51434 |
rs796991887 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387247 | AGAGAGACAGAGAGA[C/G]AGAGAGACAGAGAGA | 51434 |
rs797002895 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400111 | AAAAACAGAAAAAAA[-/A]CAACAAAAAGAGTAT | 51434 |